TY - JOUR
T1 - Site properties have a stronger influence than fire severity on ectomycorrhizal fungi and associated N-cycling bacteria in regenerating post-beetle-killed lodgepole pine forests
AU - Kennedy, Nabla M.
AU - Robertson, Susan J.
AU - Green, D. Scott
AU - Scholefield, Scott R.
AU - Arocena, Joselito M.
AU - Tackaberry, Linda E.
AU - Massicotte, Hugues B.
AU - Egger, Keith N.
N1 - Funding Information:
This project was funded by the Government of Canada through the Mountain Pine Beetle Initiative (administered by Natural Resources Canada, Canadian Forest Service) as well as a Discovery Grant from the Natural Sciences and Engineering Research Council of Canada (NSERC) to HBM. We are grateful to Ashley Gosselin, Jennifer Dupuis, Jordan Koopmans, Mark Thompson, Patrick McMechan, and Dana O’Bryan for field and laboratory assistance.
Publisher Copyright:
© 2014, Institute of Microbiology, Academy of Sciences of the Czech Republic, v.v.i.
PY - 2015/9/11
Y1 - 2015/9/11
N2 - Following a pine beetle epidemic in British Columbia, Canada, we investigated the effect of fire severity on rhizosphere soil chemistry and ectomycorrhizal fungi (ECM) and associated denitrifying and nitrogen (N)-fixing bacteria in the root systems of regenerating lodgepole pine seedlings at two site types (wet and dry) and three fire severities (low, moderate, and high). The site type was found to have a much larger impact on all measurements than fire severity. Wet and dry sites differed significantly for almost all soil properties measured, with higher values identified from wet types, except for pH and percent sand that were greater on dry sites. Fire severity caused few changes in soil chemical status. Generally, bacterial communities differed little, whereas ECM morphotype analysis revealed ectomycorrhizal diversity was lower on dry sites, with a corresponding division in community structure between wet and dry sites. Molecular profiling of the fungal ITS region confirmed these results, with a clear difference in community structure seen between wet and dry sites. The ability of ECM fungi to colonize seedlings growing in both wet and dry soils may positively contribute to subsequent regeneration. We conclude that despite consecutive landscape disturbances (mountain pine beetle infestation followed by wildfire), the “signature” of moisture on chemistry and ECM community structure remained pronounced.
AB - Following a pine beetle epidemic in British Columbia, Canada, we investigated the effect of fire severity on rhizosphere soil chemistry and ectomycorrhizal fungi (ECM) and associated denitrifying and nitrogen (N)-fixing bacteria in the root systems of regenerating lodgepole pine seedlings at two site types (wet and dry) and three fire severities (low, moderate, and high). The site type was found to have a much larger impact on all measurements than fire severity. Wet and dry sites differed significantly for almost all soil properties measured, with higher values identified from wet types, except for pH and percent sand that were greater on dry sites. Fire severity caused few changes in soil chemical status. Generally, bacterial communities differed little, whereas ECM morphotype analysis revealed ectomycorrhizal diversity was lower on dry sites, with a corresponding division in community structure between wet and dry sites. Molecular profiling of the fungal ITS region confirmed these results, with a clear difference in community structure seen between wet and dry sites. The ability of ECM fungi to colonize seedlings growing in both wet and dry soils may positively contribute to subsequent regeneration. We conclude that despite consecutive landscape disturbances (mountain pine beetle infestation followed by wildfire), the “signature” of moisture on chemistry and ECM community structure remained pronounced.
UR - http://www.scopus.com/inward/record.url?scp=84938966879&partnerID=8YFLogxK
U2 - 10.1007/s12223-014-0374-7
DO - 10.1007/s12223-014-0374-7
M3 - Article
C2 - 25540132
AN - SCOPUS:84938966879
SN - 0015-5632
VL - 60
SP - 399
EP - 410
JO - Folia Microbiologica
JF - Folia Microbiologica
IS - 5
ER -