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		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4589</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4589"/>
		<updated>2019-05-07T17:11:33Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, of which includes many important agriculture crops or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[plant roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|Interactions with arbuscular mycorrhizal fungi[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely. There aren&#039;t any known chemical controls that can be used against it but regardless, it&#039;s ability to remain dormant and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil (without AMF, or verticillium)[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.[[https://pnwhandbooks.org/plantdisease/pathogen-articles/common/fungi/verticillium-wilt-pacific-northwest]]&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt. [[https://www.mortonarb.org/trees-plants/tree-and-plant-advice/help-diseases/verticillium-wilt]]&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.[[https://ag.umass.edu/landscape/fact-sheets/verticillium-wilt]]&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833. [[https://ask.extension.org/questions/406833]]&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html. [[http://ipm.ucanr.edu/PMG/r602101511.html]]&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science. [[https://books.google.com/books?id=S0Djy-X2GTcC&amp;amp;pg=PA81&amp;amp;source=gbs_toc_r&amp;amp;cad=4#v=onepage&amp;amp;q&amp;amp;f=false]]&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/. [[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/]]&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182. [[https://www.jstor.org/stable/3756235?seq=1#metadata_info_tab_contents]]&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/. [[https://mycology.adelaide.edu.au/descriptions/ascomycetes/]]&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3. [[https://www.sciencedirect.com/science/article/pii/S0304423801003363]]&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122. [[https://www.jstor.org/stable/4353663?seq=1#metadata_info_tab_contents]]&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37. [[https://link.springer.com/article/10.1007/s10658-017-1273-y]]&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4588</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4588"/>
		<updated>2019-05-07T17:03:23Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, of which includes many important agriculture crops or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[plant roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|Interactions with arbuscular mycorrhizal fungi[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely. There aren&#039;t any known chemical controls that can be used against it but regardless, it&#039;s ability to remain dormant and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil (without AMF, or verticillium)[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt. [[https://www.mortonarb.org/trees-plants/tree-and-plant-advice/help-diseases/verticillium-wilt]]&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4546</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4546"/>
		<updated>2019-05-06T12:56:35Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Interactions with Arbuscular Mycorrhizal Fungi */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, of which includes many important agriculture crops or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[plant roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|Interactions with arbuscular mycorrhizal fungi[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely. There aren&#039;t any known chemical controls that can be used against it but regardless, it&#039;s ability to remain dormant and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil (without AMF, or verticillium)[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4171</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4171"/>
		<updated>2019-05-04T02:01:41Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. &lt;br /&gt;
&lt;br /&gt;
Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3] Leeches have well developed digestive glands called diverticula, all other annelids lack this[3].&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
Leeches are said to have evolved from ogligochaetes, they differ morphologically by having a set number of segments, rather than an ever growing number of segments. They have also lost the chaetae for movement but instead can use their anterior and posterior suckers for movement as well as feeding, which are also unique to them[9].&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
Although most polychates can regenerate lost body parts, while not entirely known, their life span is thought to last anywhere from a month to three years depending on species. This can be dependent on reproductive cycles or the fact that they are slow and cannot escape predation[3]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3]. Oligochaetes are able to regenerate lost body parts, but they do not do this forever, some earthworm species have been known to live up to ten years [3]. &lt;br /&gt;
====Hirudinea====&lt;br /&gt;
Leeches are hermaphroditic but sexually meaning both sperm and eggs are need in order for fertilization to occur. Once fertlized eggs, any nuber from 1- 100 bunched together in a cocoon, can be deposited onto rocks or vegetation.  Young leeches will hatch from the eggs. [3] &lt;br /&gt;
&lt;br /&gt;
Similarily to polychaetes not much is known about the life cycle or span of leeches. Some reproduce once and then die, and other may reproduce three times before they die[3]. &lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[[Oligochaetes]] are the primary annelids found in [[soil]], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other [[microfauna]].[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrients for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
[9]Iyer, R. G., D. V. Rogers, M. Levine, C. J. Winchell, and D. A. Weisblat. 2019. Reproductive differences among species, and between individuals and cohorts, in the leech genus Helobdella (Lophotrochozoa; Annelida; Clitellata; Hirudinida; Glossiphoniidae), with implications for reproductive resource allocation in hermaphrodites. PLOS ONE 14:e0214581.[[https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0214581]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4159</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4159"/>
		<updated>2019-05-04T01:27:17Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. &lt;br /&gt;
&lt;br /&gt;
Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3] Leeches have well developed digestive glands called diverticula, all other annelids lack this[3].&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[[Oligochaetes]] are the primary annelids found in [[soil]], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other [[microfauna]].[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
[9]Iyer, R. G., D. V. Rogers, M. Levine, C. J. Winchell, and D. A. Weisblat. 2019. Reproductive differences among species, and between individuals and cohorts, in the leech genus Helobdella (Lophotrochozoa; Annelida; Clitellata; Hirudinida; Glossiphoniidae), with implications for reproductive resource allocation in hermaphrodites. PLOS ONE 14:e0214581.[[https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0214581]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4157</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4157"/>
		<updated>2019-05-04T01:16:31Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Classification */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. &lt;br /&gt;
&lt;br /&gt;
Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3] Leeches have well developed digestive glands called diverticula, all other annelids lack this[3].&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[[Oligochaetes]] are the primary annelids found in [[soil]], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other [[microfauna]].[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4156</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4156"/>
		<updated>2019-05-04T01:15:12Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Role in Soil */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3] Leeches have well developed digestive glands called diverticula, all other annelids lack this[3].&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[[Oligochaetes]] are the primary annelids found in [[soil]], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other [[microfauna]].[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4155</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4155"/>
		<updated>2019-05-04T01:14:16Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Morphology/Anatomy */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3] Leeches have well developed digestive glands called diverticula, all other annelids lack this[3].&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4153</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4153"/>
		<updated>2019-05-04T01:11:58Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4152</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4152"/>
		<updated>2019-05-04T01:11:28Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Distribution and Habitat */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4151</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4151"/>
		<updated>2019-05-04T01:11:05Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
[[File:Leech.jpg|200px|thumb|left| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
[[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4150</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4150"/>
		<updated>2019-05-04T01:09:52Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|800px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of clitellates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] [[File:Polychaete.jpg|300px|thumb|right| Polychaete anatomy. a,b) free moving c,d) tube dwelling [8]]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Polychaetes play an important role in turnover of sediment on the ocean floor [8]. &lt;br /&gt;
&lt;br /&gt;
Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity[8].&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The larvae are usually free-living for sometime, using cilia for movement[8].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=File:Polychaete.jpg&amp;diff=4149</id>
		<title>File:Polychaete.jpg</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=File:Polychaete.jpg&amp;diff=4149"/>
		<updated>2019-05-04T01:07:32Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: Image courtesy of: https://www.britannica.com/animal/annelid/media/26308/389&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Image courtesy of: https://www.britannica.com/animal/annelid/media/26308/389&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4148</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4148"/>
		<updated>2019-05-04T01:04:26Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Parasitic */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[plant roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|Interactions with arbuscular mycorrhizal fungi[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4147</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4147"/>
		<updated>2019-05-04T00:54:32Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Morphology/Anatomy */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
The body of polychaetes is dependent on whether they are ocean-dwelling, sedentary, which live in tubes, or free-living. Most polychaetes breathe through their body wall, however some exhibit gill like structures. They also have sensory organs such as taste buds, eyes that may range in complexity.&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4146</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4146"/>
		<updated>2019-05-04T00:45:17Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Classification */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade also includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychaetes are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4145</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4145"/>
		<updated>2019-05-04T00:43:17Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Classification */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4144</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4144"/>
		<updated>2019-05-04T00:42:54Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4143</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4143"/>
		<updated>2019-05-04T00:37:47Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Sieving */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. The solution must be at room temperature for accurate readings[6]. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine was recommended to shake the solution! This was to ensure even distribution of the soil throughout the water solution.[7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
==Conclusion==&lt;br /&gt;
&lt;br /&gt;
In conclusion, performing both experiments is a good way to compare and contrast results. The gravel/sand, and silt proportions should resemble one another between the two tests, however a more accurate proportion of clay particle may be obtained from a hydrometer reading. &lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4142</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4142"/>
		<updated>2019-05-04T00:37:06Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Conclusion */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. The solution must be at room temperature for accurate readings[6]. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine was recommended to shake the solution! This was to ensure even distribution of the soil throughout the water solution.[7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
==Conclusion==&lt;br /&gt;
&lt;br /&gt;
In conclusion, performing both experiments is a good way to compare and contrast results. The gravel/sand, and silt proportions should resemble one another between the two tests, however a more accurate proportion of clay particle may be obtained from a hydrometer reading. &lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4141</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4141"/>
		<updated>2019-05-04T00:36:23Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. The solution must be at room temperature for accurate readings[6]. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine was recommended to shake the solution! This was to ensure even distribution of the soil throughout the water solution.[7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
==Conclusion==&lt;br /&gt;
&lt;br /&gt;
In conclusion, performing both experiments is a good way to compare and contrast results, the gravel/sand, and silt proportions should resemble one another between the two results, however a more accurate proportion of clay particle may be obtained from a hydrometer reading. &lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4140</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4140"/>
		<updated>2019-05-04T00:34:09Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Hydrometer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. The solution must be at room temperature for accurate readings[6]. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine was recommended to shake the solution! This was to ensure even distribution of the soil throughout the water solution.[7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4139</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4139"/>
		<updated>2019-05-04T00:21:25Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Hydrometer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine was recommended to shake the solution! This was to ensure even distribution of the soil throughout the water solution.[7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4138</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4138"/>
		<updated>2019-05-04T00:20:03Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Hydrometer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine were recommended to even shake the solution! [7]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[6], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[6], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4137</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4137"/>
		<updated>2019-05-04T00:19:32Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine were recommended to even shake the solution! [13]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[12], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[12], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;br /&gt;
&lt;br /&gt;
7. Bouyoucos, G. J. 1927. Directions for Determining the Colloidal Material of Soils by the Hydrometer Method. Science 66:16-17.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4136</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4136"/>
		<updated>2019-05-04T00:19:14Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Hydrometer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. When measuring soil samples using a hydrometer, sodium hexametaphospahte is added to the water, this acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5] This will result in a more accurate reading of sand, silt, and clay particles than could be achieved by sieving alone. &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder. &lt;br /&gt;
&lt;br /&gt;
The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. Historically, the use of a milk shake, or malt machine were recommended to even shake the solution! [13]&lt;br /&gt;
&lt;br /&gt;
The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. &lt;br /&gt;
&lt;br /&gt;
The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  &lt;br /&gt;
&lt;br /&gt;
Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. &lt;br /&gt;
&lt;br /&gt;
To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least, 12 at the most[12], however if 100% accuracy isn&#039;t need, an hour will suffice. &lt;br /&gt;
&lt;br /&gt;
The solution, with the hydrometer in it still, will then sit for at least 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[12], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample.&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4132</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4132"/>
		<updated>2019-05-03T23:59:41Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. Measuring soil samples using a hydrometer will give an accurate reading of sand silt and clay particles.  &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder.  The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. To obtain an accurate reading of clay and silt percentages the solution should sit for 6.5-8 hours at least[12], however if 100% accuracy isn&#039;t need, an hour will suffice. The solution, with the hydrometer in it still, will then sit for at least an 1-8 hours depending on the accuracy desired.  During this time the silt will settle to the bottom on the cylinder and the clay particles will remain suspended in the water[12], this suspension will allow the hydrometer to stay suspended as well and the water line will correlate to a reading which will allow the reader to determine the amount of clay in the sample. The remaining part of the proportion of sand + clay subtracted from the total soil sample will determine the amount of silt in the sample. &lt;br /&gt;
&lt;br /&gt;
The proportion of clay is able to be determined due to the sodium hexametaphospahte, which acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5]&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;br /&gt;
&lt;br /&gt;
6. Carolyn, C. B., and G. Karl. 1989. Comparison of Hydrometer Settling Times in Soil Particle Size Analysis. Journal of Range Management 42:81-83.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4130</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4130"/>
		<updated>2019-05-03T23:27:26Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Resistance */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|Interactions with arbuscular mycorrhizal fungi[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4128</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4128"/>
		<updated>2019-05-03T23:26:14Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, elm trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cotton, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As stated, there are over 200 species that may act as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4127</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4127"/>
		<updated>2019-05-03T23:25:09Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Signs and Symptoms */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
&lt;br /&gt;
A mixture of defense mechanisms from the infected host, along with enzymatic reactions from the fungus, lead to the degradation of the host vascular system[12].&lt;br /&gt;
&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4126</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4126"/>
		<updated>2019-05-03T23:21:49Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Life Cycle */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae.gif|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4125</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4125"/>
		<updated>2019-05-03T23:21:29Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
[[file: vdahliae|right|thumb|300px|frame|Life cycle of verticillium[12].]]&lt;br /&gt;
&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;br /&gt;
&lt;br /&gt;
[12]Keykhasaber, M., B. P. H. J. Thomma, and J. A. Hiemstra. 2018. Verticillium wilt caused by Verticillium dahliae in woody plants with emphasis on olive and shade trees. European Journal of Plant Pathology 150:21-37.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=File:Vdahliae.gif&amp;diff=4124</id>
		<title>File:Vdahliae.gif</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=File:Vdahliae.gif&amp;diff=4124"/>
		<updated>2019-05-03T23:18:58Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: image courtesy of: https://link.springer.com/article/10.1007/s10658-017-1273-y&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;image courtesy of: https://link.springer.com/article/10.1007/s10658-017-1273-y&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4112</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4112"/>
		<updated>2019-05-03T21:39:58Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Interactions with Arbuscular Mycorrhizal Fungi */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].  If &#039;&#039;V. dahliae&#039;&#039; is present in the rhizosphere prior to AMF introduction the AMF formation will be reduced.  However if the host plant already has mycorrhizal formation prior to verticillium infection the plant can continue to thrive and the mycorrhizal networks will not be reduced[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4111</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4111"/>
		<updated>2019-05-03T21:39:43Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Bio-Diversity */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae&#039;&#039; infected only increased the inoculation of the soil[10].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4106</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4106"/>
		<updated>2019-05-03T21:11:35Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Bio-Diversity */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3]. It has also been observed that continuous cultivation of disease susceptible host plant in areas of known &#039;&#039;V. dalihae infected only increased the inoculation of the soil. &#039;&#039;V. dahliae&#039;&#039; microscelrotia were found to germinate after being dormant for 13 years, when tried at 22 years the sclerotia did not germinate, so perhaps planting with non-susceptible plants for an extended amount of time (20-30 years) the area in question may be rid of the fungus.&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4104</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4104"/>
		<updated>2019-05-03T21:02:56Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Interactions with Arbuscular Mycorrhizal Fungi */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3] &lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4103</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4103"/>
		<updated>2019-05-03T21:02:42Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Interactions with Arbuscular Mycorrhizal Fungi */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrhizal Fungi]] ([[AMF]]) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3] &lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4102</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4102"/>
		<updated>2019-05-03T21:01:56Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the [[ascomycota]] genus of [[fungi]], more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, [[chlorosis]] (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most noticeable from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of [[Arbuscular Mycorrizhal Fungi]] ([[AMF]]) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3] &lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4101</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4101"/>
		<updated>2019-05-03T20:58:25Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Life Cycle */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the ascomycota genus of fungi, more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, chlorosis (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most nocticble from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, [[mycelia]] and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the [[cortex]] of the [[roots]], and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the [[xylem]] [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The [[hyphae]] and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of Arbuscular Mycorrizhal Fungi (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3] &lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4100</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4100"/>
		<updated>2019-05-03T20:57:22Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the ascomycota genus of fungi, more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, chlorosis (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most nocticble from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
 &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, mycelia and microsclerotia (dark, durable, resting structures which are made up of a few thick walled cells[8,11]) of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. Microscelorita are also resistant to desiccation[11]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the cortex of the roots, and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the xylem [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6]. The hyphae and conidia of verticillium cannot survive outside of the host in the soil however the microsclerotia can, and they are produced abundantly in the &amp;quot;stems of infected hosts.&amp;quot; [11]&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of Arbuscular Mycorrizhal Fungi (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
====Bio-Diversity====&lt;br /&gt;
Bio-diversity may also help in aiding infected trees, while verticillium is prevalent in many forest landscapes, plant biota aren&#039;t greatly impacted by the disease[3] &lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;br /&gt;
&lt;br /&gt;
[11]Menzies, J. D. 1963. Survival of Microbial Plant Pathogens in Soil. Botanical Review 29:79-122.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4098</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4098"/>
		<updated>2019-05-03T20:27:05Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Life Cycle and Reproduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. &lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4097</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4097"/>
		<updated>2019-05-03T20:26:24Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Polychaetes */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[8]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[8]. [[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4096</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4096"/>
		<updated>2019-05-03T20:25:57Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[11]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[11]. [[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
[8]annelid - Polychaetes.[[https://www.britannica.com/animal/polychaete]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4095</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4095"/>
		<updated>2019-05-03T20:25:22Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Polychaetes */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
&lt;br /&gt;
== Classification ==&lt;br /&gt;
&lt;br /&gt;
Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Distribution and Habitat ==&lt;br /&gt;
&lt;br /&gt;
Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
&lt;br /&gt;
[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
&lt;br /&gt;
The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. Males and females will release their gametes into the water where they are fertilized.[11]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5].&lt;br /&gt;
&lt;br /&gt;
Other polychaetes are hermaphroditic while some reproduce by budding, where a part of the adult body breaks off and mature into a new individual[11]. [[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Role in Soil ==&lt;br /&gt;
&lt;br /&gt;
[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
&lt;br /&gt;
2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
&lt;br /&gt;
3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
&lt;br /&gt;
4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
&lt;br /&gt;
5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
&lt;br /&gt;
6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
&lt;br /&gt;
[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
&lt;br /&gt;
2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
&lt;br /&gt;
3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
&lt;br /&gt;
4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
&lt;br /&gt;
5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4094</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4094"/>
		<updated>2019-05-03T19:35:07Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Resistance */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the ascomycota genus of fungi, more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, chlorosis (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most nocticble from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; exists in three life stages; dormant, parasitic, and saprophytic. &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, mycelia and microsclerotia (dark, durable, resting structures produced by the fungus[8])of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the cortex of the roots, and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the xylem [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6].&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during times of extreme heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of Arbuscular Mycorrizhal Fungi (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4093</id>
		<title>Verticillium Wilt</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Verticillium_Wilt&amp;diff=4093"/>
		<updated>2019-05-03T19:33:16Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[file: Vertfigure4composite.jpg|thumb|300px|right|Japanese Maple (Right) and Red Maple (Left) with premature fall coloring due to Verticillium Wilt[1].]]&lt;br /&gt;
Verticillium wilt is the result of a soil-borne fungal pathogen called &#039;&#039;Verticillium dahliae&#039;&#039; that infects over 200 species of plants[1]. In all there are ten recognized species of &#039;&#039;Verticillium&#039;&#039; but &#039;&#039;V. dahliae&#039;&#039; has the widest range of hosts. These can include, maple trees, tomato plants, eggplants, peach trees, black raspberry, spinach, pumpkin, alfalfa, hops, cherry trees, peony, snapdragons, chrysanthemums, etc[1]. As said there are over 200 species that acts as a host, many of which include many important agriculture crops, or forest species. &lt;br /&gt;
[[file: Maplecanker.jpg|right|thumb|100px|Maple tree with canker[4].]]&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; belongs to the ascomycota genus of fungi, more commonly known as sac-fungi[9]. Ascomycota can reproduce sexually and asexually, however &#039;&#039;V. dahliae&#039;&#039; reproduce asexually though conidia[9].&lt;br /&gt;
&lt;br /&gt;
=Signs and Symptoms=&lt;br /&gt;
[[file: Longsectionalvwilt.jpg|left|thumb|100px|frame|Long cross section of branch infected with verticillium[1].]]&lt;br /&gt;
There are many signs and symptoms of Verticillium Wilt that a host plant may exhibit. These include, wilting of the leaves, chlorosis (yellowing of the leaves), stunted plant growth[1], the edges of the leaves my appear &amp;quot;scorched&amp;quot; or brown, and dead twigs and branches may appear. Specifically on maples areas of dead bark, called cankers, may appear[2].&lt;br /&gt;
[[file: Crosssectionalvwilt.jpg|right|thumb|100px|frame|Cross section of branch infected with verticillium[1].]]&lt;br /&gt;
&lt;br /&gt;
These symptoms may appear on one side of the plant as a whole, one branch, or one grouping of leaves. Symptoms are most nocticble from mid to late summer or during times of extreme heat or drought[1]. &lt;br /&gt;
&lt;br /&gt;
Symptoms expressed are dependent on the host for example, in spinach or cauliflower symptoms don&#039;t appear until the plant begins to flower[1].&lt;br /&gt;
&lt;br /&gt;
When a cross section is taken, infected branches on trees will show dark green or brown rings[1]. This is because verticillium infects and spreads through the vascular systems of its hosts, this disrupts the water and mineral transportation to the branches and leaves of the hosts[3]. While vascular staining occurs often, it is not always present[3].&lt;br /&gt;
=Life Cycle=&lt;br /&gt;
&#039;&#039;V. dahliae&#039;&#039; exists in three life stages; dormant, parasitic, and saprophytic. &lt;br /&gt;
====Dormant====&lt;br /&gt;
In its dormant phase, mycelia and microsclerotia (dark, durable, resting structures produced by the fungus[8])of the fungus are capable of surviving in dried conditions, they can survive in soil away from a host or embedded in fragments of tissue[6]. The structures will be ready to germinate once in the presence of a host[7]. The microsclerotia can either stand alone, become embedded in plant leaves or branches; once the branches or leaves die and fall off the tree they can be transported by wind to other places[3]. Because microsclerotia allow verticillium to lie dormant for a long time, it is highly unlikely that the soil it is infecting will ever be rid of the fungus. The only way to avoid infecting plants are to plant species that are not susceptible to infection by the fungus[3]. &lt;br /&gt;
====Parasitic====&lt;br /&gt;
Verticillium infects its host by entering the host through the cortex of the roots, and grows as a mass of mycelia towards the xylem, from there most times it will continue to travel up the xylem [6]. Once the hyphae invade the vessels, the fungus reproduces asexually through conidia, the conidia can then travel from its start point in the xylem throughout the entire plant[6,9]. Verticillium will only infect health roots, it has been previously believed that it&#039;s a wound infection, however it is not[6].&lt;br /&gt;
=Resistance=&lt;br /&gt;
 [[file: AMF.JPG|right|thumb|300px|[10].]]Controlling &#039;&#039;V. dahliae&#039;&#039; is very unlikely, there aren&#039;t any known chemical controls that can be used against it, regardless it&#039;s ability to remain dormant, and widespread throughout soil would make use of such treatments futile. Crop rotation with plants that are resistant to the fungus is suggested as to break up the establishment verticillium has among non-resistant hosts[9].It has also been found that when fields are flooded especially during time of great heat, inoculation of host plants was much lower, perhaps due to the stress put on the plant (remember verticillium infects healthy roots)[9].&lt;br /&gt;
====Interactions with [[Arbuscular Mycorrhizal Fungi]]====&lt;br /&gt;
In a study done to observe the effects of Arbuscular Mycorrizhal Fungi (AMF) on plants infected with &#039;&#039;V. dahliae&#039;&#039; it was found that AMF greatly helped the infected plant. In this study they observed an eggplant and tomato plant, each of which had a control &lt;br /&gt;
(one growing in neutral soil), one infected with verticillium, one infected with AMF, and the last was infected with both AMF and verticillium. While the plant only infected with AMF did substantially better than the other three in both the tomato and eggplant, the AMF and veritcillium infected plants still did better than the plants growing in neutral soil without AMF, or verticillium[10].&lt;br /&gt;
====N,K,P Availability====&lt;br /&gt;
It has been found that cotton plants, which are susceptible to verticillium infection, were more resistant when there were high levels of potassium (K), and the disease was more damaging when there were higher level of nitrogen (N)[9].&lt;br /&gt;
&lt;br /&gt;
=References=&lt;br /&gt;
&lt;br /&gt;
[1]Dung, Jeremiah K.S., and Jerry Weiland. “Verticillium Wilt in the Pacific Northwest.” Pacific Northwest Pest Management Handbooks, OSU &lt;br /&gt;
Extension Service - Extension and Experiment Station Communications, 13 Oct. 2016, pnwhandbooks.org/plantdisease/pathogen- &lt;br /&gt;
articles/common/fungi/verticillium-wilt-pacific-northwest.&lt;br /&gt;
&lt;br /&gt;
[2]“Verticillium Wilt.” Verticillium Wilt | The Morton Arboretum, www.mortonarb.org/trees-plants/tree-and-plant-advice/help-   diseases/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[3]Brazee, Nicholas. “Verticillium Wilt.” Center for Agriculture, Food and the Environment, 26 Feb. 2018, ag.umass.edu/landscape/fact- &lt;br /&gt;
sheets/verticillium-wilt.&lt;br /&gt;
&lt;br /&gt;
[4]Anita. “Silver Maple - Bleeding Canker? - Ask an Expert.” EXtension, 14 June 2017, ask.extension.org/questions/406833.&lt;br /&gt;
&lt;br /&gt;
[5]Gubler, W D, and B L Teviotdale. “How to Manage Pests.” UC IPM Online, University of California, ipm.ucanr.edu/PMG/r602101511.html.&lt;br /&gt;
&lt;br /&gt;
[6]Mace, M. 2012. Fungal Wilt Diseases of Plants. Elsevier Science.&lt;br /&gt;
&lt;br /&gt;
[7]Inderbitzin, Patrik, et al. “Phylogenetics and Taxonomy of the Fungal Vascular Wilt Pathogen Verticillium, with the Descriptions of Five New Species.” PloS One, Public Library of Science, 7 Dec. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3233568/.&lt;br /&gt;
&lt;br /&gt;
[8]Gordee, R. S., and C. L. Porter. 1961. Structure, Germination, and Physiology of Microsclerotia of Verticillium albo-atrum. Mycologia 53:171-182.&lt;br /&gt;
&lt;br /&gt;
[9]“Ascomycota.” Ascomycota | Mycology Online, University of Adelaide, 15 May 2001, mycology.adelaide.edu.au/descriptions/ascomycetes/.&lt;br /&gt;
&lt;br /&gt;
[10]Karagiannidis, Nikitas, et al. “Effect of Verticillium Wilt (Verticillium Dahliae Kleb.) and Mycorrhiza (Glomus Mosseae) on Root Colonization, Growth and Nutrient Uptake in Tomato and Eggplant Seedlings.” Scientia Horticulturae, vol. 94, no. 1-2, 2002, pp. 145–156., doi:10.1016/s0304-4238(01)00336-3.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4092</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4092"/>
		<updated>2019-05-03T19:30:27Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Hydrometer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
&lt;br /&gt;
Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
&lt;br /&gt;
===Hydrometer===&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Clay]] particles are made up of either three or four charged ions, because of this they tend to cling to one another [3], this tendency is called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. Measuring soil samples using a hydrometer will give an accurate reading of sand silt and clay particles.  &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder.  The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. The solution, with the hydrometer in it still, will then sit for at least an hour, the reading on the hydrometer will show the amount of clay in the sample, and the remainder of the sample will be silt. &lt;br /&gt;
&lt;br /&gt;
The proportion of clay is able to be determined due to the sodium hexametaphospahte, which acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5]&lt;br /&gt;
&lt;br /&gt;
===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
&lt;br /&gt;
2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
&lt;br /&gt;
3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
&lt;br /&gt;
4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
&lt;br /&gt;
5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4091</id>
		<title>Soil Particle Size Analysis Methods</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Soil_Particle_Size_Analysis_Methods&amp;diff=4091"/>
		<updated>2019-05-03T19:27:05Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: /* Sieving */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Soil Particle Size Analysis Methods==&lt;br /&gt;
&lt;br /&gt;
[[File:sieve.jpg|left|thumb|caption|US Standard Sieve]]&lt;br /&gt;
&lt;br /&gt;
There are three basic classifications of [[soil]] particle size. They include [[clay]], [[silt]] and [[sand]], from smallest to largest, respectively. There are several different methods to determining how much clay, silt and sand is in a sample of soil, two include sieving, and another which uses a hydrometer. There is another method used in determining the amount of organic mater in soil, to do this one might use the [[Loss on Ignition]] test, however the purpose of this article will be to focus on clay, silt and sand only.  &lt;br /&gt;
&lt;br /&gt;
===Sieving===&lt;br /&gt;
&lt;br /&gt;
To begin, the soil sample needs to be dried to a constant weight, for 24 hrs at 120˚F this will eliminate all the moisture held in the soil.&lt;br /&gt;
Once the soil is dried to constant weight, the sieving can begin. The sieves come with different size screens and they should be chosen according to the particles that are to be isolated.  &lt;br /&gt;
&lt;br /&gt;
There should be one sieve on top with larger holes to accommodate for gravel that is in the soil. Gravel includes any particle larger than 2mm and will be considered as &amp;quot;sand&amp;quot;. [1]&lt;br /&gt;
[[File:sievestack.jpeg|right|thumb|caption|Stacked Sieve: largest screen size at the top, smallest screen sieve at the bottom]]&lt;br /&gt;
&lt;br /&gt;
Course sand particles range from 1.0 - 2.0 mm while very fine sand particles range from 0.05 - 0.10mm.[1] Choosing two or more sieves within that range might be helpful to account for larger or smaller sand particles; for instance, include a sieve at 2.0mm and one at 0.05mm. &lt;br /&gt;
Silt particles ranges from 0.05mm - 0.002 mm [1], therefore a sieve with a corresponding screen hole size of 0.002 mm should suffice.&lt;br /&gt;
&lt;br /&gt;
Lastly, clay particles are anything smaller than 0.002mm. [1] At the bottom of the stack of sieves should be placed a bottom container with a solid bottom to collect the clay particle that will sift past the 0.002mm sieve.  &lt;br /&gt;
&lt;br /&gt;
Once the sieves are set up, the soil sample that has been dried to a constant weight will be sifted through the sieves using a sieve shaker. After about 15-20 min of shaking the soil should be separated into gravel, sand, silt and clay. The proportions can then be calculated to determine how much of each particle is one soil sample. For instance, 26g sand/50g total soil = 52% sand.&lt;br /&gt;
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Soil sieving is a purely mechanical process of determining soil particle size in a sample of soil. [2] A better method to accurately separating clay particles from the soil would be to use a hydrometer.&lt;br /&gt;
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===Hydrometer===&lt;br /&gt;
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Because [[clay]] particles are made up of either three or four charged ions, they tend to cling to one another [3], this being called flocculation[4].  This can sometimes pose a problem when trying to accurately determine the proportion of clay particles in a sample of soil. Measuring soil samples using a hydrometer will give an accurate reading of sand silt and clay particles.  &lt;br /&gt;
[[File:hydrometer.jpg|right|thumb]]&lt;br /&gt;
To measure using a hydrometer, a solution of water mixed with sodium hexametaphosphate is prepared and poured into a 1000ml graudated cylinder.  The soil sample (for example 50g soil) is then poured into the solution and shaken or stirred until evenly distributed. The hydrometer is then placed in the graduated cylinder, and a measurement is read off of it after 40 seconds. The hydrometer is then taken out and the solution of soil, water, and sodium hexmetaphosphate it stirred or shaken again.  Another 40 second reading will be taken and then an average of the two readings will be calculated to determine the amount of sand (and gravel) in the sample. The solution, with the hydrometer in it still, will then sit for at least an hour, the reading on the hydrometer will show the amount of clay in the sample, and the remainder of the sample will be silt. &lt;br /&gt;
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The proportion of clay is able to be determined due to the sodium hexametaphospahte, which acts as a defloccuant, meaning the clay particle ions will now repulse each other instead of clinging to one another. [4,5]&lt;br /&gt;
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===References=== &lt;br /&gt;
1. Whiting, David, et al. Estimating Soil Texture. 2003, Estimating Soil Texture, culter.colorado.edu/~kittel/SoilChar(&amp;amp;RibbonTest)_handout.pdf.&lt;br /&gt;
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2. “Particle Size Analysis (for Soils/Sediments).” UCL Department of Geography, www.geog.ucl.ac.uk/resources/laboratory/laboratory- &lt;br /&gt;
methods/particle-size-analysis/particle-size-analysis-for-soils-sediments.&lt;br /&gt;
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3. “1.8 Clay Mineral Structure.” Fundamentals of Soil Ecology, by David C. Coleman et al., Academic Press, 2018.&lt;br /&gt;
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4. Tozzi, Nilo. “Deflocculants: A Detailed Overview.” Deflocculants: A Detailed Overview, digitalfire.com/4sight/education/deflocculants_a_detailed_overview_324.html.&lt;br /&gt;
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5. Andreola, Fernanda, et al. “The Role of Sodium Hexametaphosphate in the Dissolution Process of Kaolinite and Kaolin.” Journal of the European Ceramic Society, Elsevier, 24 Sept. 2003, www.sciencedirect.com/science/article/pii/S0955221903003662.&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
	<entry>
		<id>https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4090</id>
		<title>Annelids</title>
		<link rel="alternate" type="text/html" href="https://soil.evs.buffalo.edu/index.php?title=Annelids&amp;diff=4090"/>
		<updated>2019-05-03T17:51:24Z</updated>

		<summary type="html">&lt;p&gt;Taylorga: &lt;/p&gt;
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&lt;div&gt;Annelids, or segmented worms, are segmented bilaterian invertebrates that are very important to a variety of marine and terrestrial environments. All annelids have a central body cavity called a coelom, bristles called setae, and segments called annulations which they are named after. There are three major groups of of annelids; the class Polychaeta which are almost entirely marine in nature and the subclasses of  Oligochaeta which are earthworms and their relatives, and Hirudinea which are leeches. Among these groups there are approximately 17,000 described species. Many of the species of annelids reproduce sexually and are hermaphroditic, but some are able to asexually reproduce. Annelids are found across the entire planet in almost every kind of environment imaginable. Annelids are generally soft tissue organisms, but there is evidence of them in the fossil record dating back to the Ordovician period.[[File:Annelida.png|600px|thumb|right|]]&lt;br /&gt;
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== Classification ==&lt;br /&gt;
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Annelids belong to the clade Lophotrochozoa. This clade includes the phyla Mollusca, Sipuncula, Brachiopodia, and Phorondia. [1] The two major groups of &lt;br /&gt;
annelids are the clitellates and polychaetes. Clitellates include members of the subclasses oligochaeta (eg. earthworms) and hirundinea (leeches). Oligochaetea are primarily terestrial, preferring damp soil, while leeches are mostly made up of freshwater aquatic species. Polychaetes are almost entirely made up of marine species, but a few freshwater species do exist.[1] There are abut 17,000 species of annelid and about 12,000 of them are members of polychaetes. Polychates are then divided into two groups dependent on if they are mostly mobile throughout life or if they live in tubes or burrows for the majority of their existence. There are also about 42 different groups of cilliates[2].[[File:Leech.jpg|200px|thumb|right| &#039;&#039;Haemadipsa picta&#039;&#039; or the Tiger Leech member of the hirundinea subclass]]&lt;br /&gt;
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== Distribution and Habitat ==&lt;br /&gt;
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Annelids, due to their incredible diversity, live in nearly every habitat on planet, however they have no means of protecting themselves from desiccation, therefore they prefer to live in wet environments. These environments include oceanic sea floors, freshwater systems, and damp soil.[3] The class Polychaeta are primarily benthic [[organisms]] that can live in saline, brackish, or freshwater environments. Their distribution in these areas are primarily controlled by the space available to them, the dissolved oxygen content in the water, the rate of movement of the water, and the relative salinity and temperature of the water to the Polychaeta.[4] Oligochaetes are primarily found in the soil but a few are found in aquatic environments, and leeches are almost entirely aquatic or limited to humid areas.[3]&lt;br /&gt;
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== Morphology/Anatomy ==&lt;br /&gt;
Annelids are bilaterally symmetrical [[animals]]. The entire body of an annelid is composed of segments. They are named after the Latin word &amp;quot;anellus&amp;quot; which means little ring.[2] These segments can grow in number as the annelid grows in length, with exception of leeches which can have 34 segments and grow by expanding those 34 segments.[3] Annelids also have setae, or chaetae, which are long filaments or hooked structures made up up many chitinous cylinders held together by sclerotinized proteins.[2] These seatae are important in anchoring the annelids down and to help them move up surfaces. &lt;br /&gt;
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[[File:EarthwormCrossSection.jpg|200px|thumb|left| Cross section of an earthworm]]&lt;br /&gt;
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The digestive tract of an annelid is essentially one tube that runs from the mouth of the organism to the anus. The area between the inner cavity and the outside of the annelid is called the coelem. This area is filled with a coelemic fluid that also contains the other organ systems of the animals. This fluid is very important for a variety of functions of the organism such as locomotion, osmoregulation, and multiple metabolic processes among others. In polychaetes this fluid is also used to keep the worm&#039;s salt levels similar to the surrounding water. The coelmic fluids of leeches are filled with connective tissue and becomes more so as the leech ages. Oxygen is generally absorbed through the skin of the annelid and passed through the body by a closed circulatory system.[3]&lt;br /&gt;
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== Life Cycle and Reproduction ==&lt;br /&gt;
[[File:Earthwormsmating.jpg|200px|thumb|Left|Two earthworms exchanging sperm.]]&lt;br /&gt;
====Polychaetes====&lt;br /&gt;
Many terrestrial annelids are hermaphroditic however, many polychaetes have defined male and female sexes for spawning[2].  Polychaete spawn near the surface marine environments. When they want to spawn they will swim to the surface and the females will release the eggs and the males will fertilize them.[5]  The worms then undergo various stages of development under the protection of their mother until they are fully developed displaying a type of brooding behavior[5]. [[File:Bobbit Worm.jpg|200px|thumb|Right|&#039;&#039;Eunice aphroditois&#039;&#039; &lt;br /&gt;
or the Bobbit Worm, an aquatic predatory polychaete worm that buries beneath sediments to ambush prey]]&lt;br /&gt;
====Oligochaetes====&lt;br /&gt;
Oligochaetes are also hermaphroditic, each individual posses both male and female reproductive organs. While they may appear to reproduce sexually, they are instead exchanging sperm which is then stored in sperm sacs[7]. The sperm is later released along with the eggs into a cocoon initially located on the clitellum. Other oligochaetes can reproduce parthenogenetically without fertilization by sperm[7]. Oligochaetes do not undergo a larval stage rather they simply exit the cocoon as small oligochaetes and grow larger as they become more mature[3].&lt;br /&gt;
====Hirudinea====&lt;br /&gt;
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== Role in Soil ==&lt;br /&gt;
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[Oligochaetes] are the primary annelids found in [[soil], there are believed to be more than 5,000 earthworm species[7]. Earthworms are considered ecosystem engineers because of the role they play in the structure of soils and the diversity of the soil ecosystem. Earthworms either get their food from the surface leaf litter or the organic residue found in soil.[6] The majority of organics that an earthworm will ingest are from dead plant matter, but they will also consume living animals such as [[nematodes]] and other microfauna.[6] Earthworms prefer foods with a high nitrogen content and they also eat to burrow as well. As they burrow they leave nutrient rich casts which are important for returning nutrients to the soil. This aerates the soil, provides more nutrient for living plants, and helps prevent erosion. These nutrient rich casts are a big reason why earthworms are important to agriculture and why they are sought out when planting an new field.[6]&lt;br /&gt;
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== References ==&lt;br /&gt;
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1. Parry, L. , Tanner, A. , Vinther, J. and Smith, A. (2014), The origin of annelids. Palaeontology, 57: 1091-1103. doi:10.1111/pala.12129&lt;br /&gt;
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2. Rouse, G. W. (2001). Annelida (Segmented Worms). In eLS, (Ed.). doi:10.1038/npg.els.0001599&lt;br /&gt;
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3. Reish, D. J. (2013, December 18). Annelid. Retrieved April 12, 2018, from https://www.britannica.com/animal/annelid&lt;br /&gt;
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4. Lardicci, C. , Abbiati, M. , Crema, R. , Morri, C. , Bianchi, C. N. and Castelli, A. (1993), The Distribution of Polychaetes Along Environmental Gradients: An Example from the Or betel I o Lagoon, Italy. Marine Ecology, 14: 35-52. doi:10.1111/j.1439-0485.1993.tb00363.x&lt;br /&gt;
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5. Annie Mercier, Sandrine Baillon, Jean-François Hamel,Life history and seasonal breeding of the deep-sea annelid Ophryotrocha sp. (Polychaeta: Dorvelleidae),Deep Sea Research Part I: Oceanographic Research Papers,Volume 91,2014,Pages 27-35,ISSN 0967-0637,https://doi.org/10.1016/j.dsr.2014.05.007.&lt;br /&gt;
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6. Lenardt, A. (2014, April 7). The Role of Earthworms in Soil Systems. Retrieved April 14, 2018, from https://blogs.unbc.ca/biol202/2014/04/07/the-role-of-earthworms-in-soil-systems/&lt;br /&gt;
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[7]“4.4 The Macrofauna.” Fundamentals of Soil Ecology, by David C. Coleman et al., Elsevier ; London, 2018, pp. 132–168.&lt;br /&gt;
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&#039;&#039;Image Sources&#039;&#039;&lt;br /&gt;
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1.Taken By Phynix Davis in Roosevelt Park on 4/14/2018&lt;br /&gt;
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2.https://imgur.com/gallery/7oQDJ&lt;br /&gt;
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3. http://www.savalli.us/BIO385/Diversity/09.Annelida.html&lt;br /&gt;
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4.http://www.soilanimals.com/look/soil-food-web&lt;br /&gt;
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5. https://www.mnn.com/earth-matters/animals/stories/bobbitt-worm-blue-planet&lt;/div&gt;</summary>
		<author><name>Taylorga</name></author>
	</entry>
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