|Forest Investment Account (FIA) - Forest Science Program|
|FIA Project Y091075|
|Mycorrhizal fungi: unlocking its ecology and role for the establishment and growth performance of different conifer species in coastal ecosystems|
|Project lead: Simard, Suzanne (University of British Columbia)|
|Subject: Forest Investment Account (FIA), British Columbia|
|Series: Forest Investment Account (FIA) - Forest Science Program|
|This proposed PhD project examines the ecology of mycorrhizal associations in two contrasting coastal ecosystems, one dominated by western redcedar and the other by western hemlock, to understand how it influences seedling establishment of different tree species. It will contribute to the forestry regeneration project known as the Salal Cedar Hemlock Integrated Research Project (SCHIRP), which is addressing well-known regeneration problems of conifers on northern Vancouver Island (http://www.forestry.ubc.ca/schirp/homepage.html). One objective of SCHIRP is to identify factors and underlying ecological mechanisms differentiating Cedar-Hemlock (CH) and Hemlock-Amabilis fir (HA) ecosystems that influence the growth and nutrient acquisition of different regenerating conifer species (Prescott, 1996; Mallik & Prescott, 2001; Blevins & Prescott, 2002). A new objective, initiated by Western Forest Products, is to refine the biogeoclimatic ecological classification (BEC) system and associated ecosystem-based interpretations for improved forest management (McWilliams & Klinka, 2005; McWilliams et al., 2007).|
Mycorrhizal associations between symbiotic fungi and tree roots are crucial for seedling nutrient uptake, survival and growth, and tree productivity in nutrient-limited environments (van der Heijden et al., 1998; Jonsson et al., 2001; Read & Perez-Moreno, 2003). Two dissimilar mycorrhizal associations we will study are arbuscular mycorrhizae (AM), which colonize western redcedar, and ectomycorrhizae (EM), which associate with western hemlock. AM and EM fungal species are biologically distinct, with AM fungi forming intra-cellular arbuscules and EM fungi forming an extra-cellular Hartig net, both serving as sites for nutrient-carbon exchange with the host tree. Cedar and hemlock have strict fidelity to its specific class (AM vs EM) of fungi (Molina et al. 1992), but potentially with considerable fungal species variability within each class. We hypothesize that the class of mycorrhizal inoculum present in the soil is governed by the dominant host tree species, such that CH sites dominated by cedar contain predominantly AM inoculum, whereas HA sites dominated by hemlock contain predominantly EM inoculum. Preliminary surveys suggest there is a strong correlation between dominance by AM or EM classes of fungi and the ability for cedar and hemlock seedlings to become established following harvest. On cedar-origin sites, for example, low EM inoculum potential would limit establishment of hemlock, matching field observations. Further study is required to confirm this hypothesis.
Our questions are:
1. Are there differences in AM and EM fungal communities or inoculum potential between CH and HA sites?
2. How does mycorrhizal inoculum of different ecosystems influence seedling establishment, survival, foliar nutrients and growth?
3. Can modifying mycorrhizal inoculum at the time of planting improve seedling establishment?
There are two parts to this project. The first part involves the molecular characterization of mycorrhizal fungal communities within adjacent CH and HA ecosystems of old growth, clear-cut and regenerating sites, and determining inoculum potential. This will enhance earlier work involving molecular characterization of EM fungi on hemlock saplings in fertilized and control sites at the SCHIRP study area, where it was discovered that legacy effects of fertilization on tree growth persisted for many years in the fungal community (Wright 2006). Here, we will augment this earlier research by expanding the fungal community characterization to old-growth and newly regenerating forests, and to include western redcedar as well as western hemlock. The second part of this project involves planting cedar and hemlock seedlings at each CH and HA clearcut site with (a) soil transferred from hemlock, and (b) soil transferred from cedar forests nearby. This study will be repeated in the greenhouse under a common garden environment. For each study, mycorrhizal colonization, composition and diversity will be evaluated using microscopic and molecular techniques, and these parameters will be related to seedling performance. The results will be used to inform management interpretations of the new ecological classification that is being developed for the area. Interpretations will include recommendations for choice of tree species to regenerate (informing stocking standards) as well as choice of fungal inoculants to add at the time of planting.
Blevins LL, Prescott CE 2002. Salal Cedar Hemlock Integrated Research Program Update #2: Silvicultural Practises for Regeneration of Cedar-Hemlock Sites in Coastal British Columbia.In. Vancouver, B.C.: University of British Columbia.
Jonsson LM, Nilsson M-C, Wardle DA, Zackrisson O. 2001. Context dependent effects of ectomycorrhizal species richness on tree seedling productivity. Oikos 93: 353-364.
Mallik AU, Prescott CE. 2001. Growth inhibitory effects of salal on western hemlock and western red cedar. Agronomy Journal 93(1): 85-92.
McWilliams J, Green B, Lewis T. 2007. Phase II Review of Ecosystem Classification in TFL6.In. Vancouver: B.A. Blackwell and Associates Ltd., prepared for Western Forest Products Inc. 1-103.
McWilliams J, Klinka K. 2005. Site identification of the SCHIRP plots using the Biogeoclimatic Ecosystem Classification system.In. Vancouver, Canada: Internal report. B.A. Blackwell and Associates Ltd.
Molina R, Massicotte H, Trappe JM. 1992. Specificity phenomena in mycorrhizal symbioses: community-ecological consequences and practical implications. In MF Allen, Mycorrhizal Functioning: An Integrative Plant-fungal Process. Springer, ISBN 0412018918. 552 pp.
Prescott CE 1996. A field guide to regeneration of salal-dominated cedar-hemlock (CH) sites in the CWHvm1.In. Vancouver B.C.: University of British Columbia. 1-83.
Read DJ, Perez-Moreno J. 2003. Mycorrhizas and nutrient cycling in ecosystems – a journey towards relevance? New Phytologist 157: 475-492.
van der Heijden MGA, Klironomos JN, Ursic M, Moutoglis P, Streitwolf-Engel R, Boller T, Wiemken A, Sanders IR. 1998. Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature 396: 69-72.
Wright SHA. 2006. Long-term effects of nitrogen and phosphorus fertilization on ectomycorrhizal diversity of 18-year-old western hemlock (Tsuga heterophylla) on northern Vancouver Island. Master's thesis, University of British Columbia Vancouver.
|Related projects:  FSP_Y102075,  FSP_Y113075|
|Contact: Simard, Suzanne, (250) 352-0601, firstname.lastname@example.org|
|Executive summary (16Kb)|
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Updated May 02, 2011
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