Spatial ecology of ectomycorrhizal fungal communities
Ectomycorrhizal (ECM) fungi evolved recently (about 150 million years ago), in many separate events, from saprotrophic fungi (brown‐rot, white‐rot and litter decaying) (Hibbett et al., 2000; Wang and Qiu, 2006; Tedersoo et al., 2010a; Kohler et al., 2015). Their importance to host carbon and nutrien...
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ftunivwestsyd:oai:researchdirect.westernsydney.edu.au:uws_38697 2023-05-15T15:08:37+02:00 Spatial ecology of ectomycorrhizal fungal communities Pickles, Brian J. Anderson, Ian C. (R10589) Martin, Francis (Editor) Hawkesbury Institute for the Environment (Host institution) 2016 print 24 http://ebookcentral.proquest.com/lib/uwsau/reader.action?ppg=385&docID=4729653&tm=1487046393940 http://handle.westernsydney.edu.au:8081/1959.7/uws:38697 eng eng U.S., Wiley-Blackwell Molecular Mycorrhizal Symbiosis--9781118951415--9781118951422 pp: 363-386 XXXXXX - Unknown ectomycorrhizal fungi fungal communities spatial ecology book chapter 2016 ftunivwestsyd 2020-12-05T17:11:10Z Ectomycorrhizal (ECM) fungi evolved recently (about 150 million years ago), in many separate events, from saprotrophic fungi (brown‐rot, white‐rot and litter decaying) (Hibbett et al., 2000; Wang and Qiu, 2006; Tedersoo et al., 2010a; Kohler et al., 2015). Their importance to host carbon and nutrient cycling has been well documented (Smith and Read, 2008), but remains an area of fruitful research. ECM fungi associate with approximately 2% of known plant species, but those species tend to be large, woody, and dominant members of global ecosystems (Brundrett, 2009). Although research on ECM systems has typically focused on northern hemisphere temperate and boreal forests, the symbiosis is widespread, occurring in arctic, tundra, Mediterranean and tropical ecosystems as a result of biogeographical processes (Taylor and Alexander, 2005) and, in some cases, human intervention (e.g., Hayward et al., 2014). Physiologically, ECM fungi form structures that exist along a gradient from the microscopic (e.g., spores, individual hyphae, Hartig net) to the macroscopic (e.g., clusters of ECM root tips, tubercules, rhizomorphs, mycelial networks and sporocarps; Smith and Read, 2008). Thus, due to their biology, they have the potential to display multiple levels of spatial organization simultaneously. Understanding these different levels of organization, and how ECM fungi interact with their hosts, the soil environment, and other trophic groups, is key to making inferences about their biology and their impact on ecosystem‐level ecological processes. Book Part Arctic Tundra University of Western Sydney (UWS): Research Direct Arctic Hayward ENVELOPE(167.350,167.350,-78.117,-78.117) |
institution |
Open Polar |
collection |
University of Western Sydney (UWS): Research Direct |
op_collection_id |
ftunivwestsyd |
language |
English |
topic |
XXXXXX - Unknown ectomycorrhizal fungi fungal communities spatial ecology |
spellingShingle |
XXXXXX - Unknown ectomycorrhizal fungi fungal communities spatial ecology Pickles, Brian J. Anderson, Ian C. (R10589) Spatial ecology of ectomycorrhizal fungal communities |
topic_facet |
XXXXXX - Unknown ectomycorrhizal fungi fungal communities spatial ecology |
description |
Ectomycorrhizal (ECM) fungi evolved recently (about 150 million years ago), in many separate events, from saprotrophic fungi (brown‐rot, white‐rot and litter decaying) (Hibbett et al., 2000; Wang and Qiu, 2006; Tedersoo et al., 2010a; Kohler et al., 2015). Their importance to host carbon and nutrient cycling has been well documented (Smith and Read, 2008), but remains an area of fruitful research. ECM fungi associate with approximately 2% of known plant species, but those species tend to be large, woody, and dominant members of global ecosystems (Brundrett, 2009). Although research on ECM systems has typically focused on northern hemisphere temperate and boreal forests, the symbiosis is widespread, occurring in arctic, tundra, Mediterranean and tropical ecosystems as a result of biogeographical processes (Taylor and Alexander, 2005) and, in some cases, human intervention (e.g., Hayward et al., 2014). Physiologically, ECM fungi form structures that exist along a gradient from the microscopic (e.g., spores, individual hyphae, Hartig net) to the macroscopic (e.g., clusters of ECM root tips, tubercules, rhizomorphs, mycelial networks and sporocarps; Smith and Read, 2008). Thus, due to their biology, they have the potential to display multiple levels of spatial organization simultaneously. Understanding these different levels of organization, and how ECM fungi interact with their hosts, the soil environment, and other trophic groups, is key to making inferences about their biology and their impact on ecosystem‐level ecological processes. |
author2 |
Martin, Francis (Editor) Hawkesbury Institute for the Environment (Host institution) |
format |
Book Part |
author |
Pickles, Brian J. Anderson, Ian C. (R10589) |
author_facet |
Pickles, Brian J. Anderson, Ian C. (R10589) |
author_sort |
Pickles, Brian J. |
title |
Spatial ecology of ectomycorrhizal fungal communities |
title_short |
Spatial ecology of ectomycorrhizal fungal communities |
title_full |
Spatial ecology of ectomycorrhizal fungal communities |
title_fullStr |
Spatial ecology of ectomycorrhizal fungal communities |
title_full_unstemmed |
Spatial ecology of ectomycorrhizal fungal communities |
title_sort |
spatial ecology of ectomycorrhizal fungal communities |
publisher |
U.S., Wiley-Blackwell |
publishDate |
2016 |
url |
http://ebookcentral.proquest.com/lib/uwsau/reader.action?ppg=385&docID=4729653&tm=1487046393940 http://handle.westernsydney.edu.au:8081/1959.7/uws:38697 |
long_lat |
ENVELOPE(167.350,167.350,-78.117,-78.117) |
geographic |
Arctic Hayward |
geographic_facet |
Arctic Hayward |
genre |
Arctic Tundra |
genre_facet |
Arctic Tundra |
op_relation |
Molecular Mycorrhizal Symbiosis--9781118951415--9781118951422 pp: 363-386 |
_version_ |
1766339941676089344 |