Brian J. Wilsey
B.S. 1986 Henderson State University
M.S. 1988 Louisiana State University
Ph.D. 1995 Syracuse University
Title and Mailing Address:
Associate Professor, Department of
Ecology, Evolution, and Organismal
Biology,
253 Bessey Hall,
Iowa State University, Ames, IA 50011-1020
Office: 131 Bessey Hall
Lab: 40 Bessey Hall
Phone: (515)294-0232
Fax: (515)294-1337
E-mail: bwilsey@iastate.edu
RESEARCH INTERESTS
In the Wilsey lab, we are interested in the ecology of prairie
grasslands. Tallgrass prairies are among the most
species-diverse ecosystems. We commonly count 20-30 plant species in Iowa
within small
quadrats (0.4 m2), and most small prairies (< 10 ha) support more than one
hundred species (
Martin et al. 2005, Wilsey et al. 2005a). It is
still
largely unknown how this very high species diversity develops and is
maintained over time. Developing a better understanding of mechanisms behind
diversity maintenance is a central focus of work in the lab (e.g. Wilsey et al.
2005, Polley et al. 2005, Martin and
Wilsey 2006, Isbell et al. 2009, Wilsey et al. 2009).
Furthermore, we
are studying how changes in
species diversity influence community stability and ecosystem process rates
(i.e. ecosystem services).
Information from
our studies will be useful in the management and
restoration of
grassland ecosystems.
Loess Hills, Iowa (Sylvan Runkel
Preserve)
Is plant diversity an important predictor of ecosystem process rates?
Biodiversity is declining worldwide from human activities. In recent years,
ecologists have focused on how species
composition and diversity may impact community and ecosystem processes.
Species
composition and diversity may influence processes independently of, or
interactively with, the abiotic components of the environment. Species
diversity has two components, 1) richness, or the number
of species in a given area, and 2) evenness, or how evenly distributed biomass
or abundance is among species. Several high profile studies in the 1990's
found
that net primary productivity and resistance to invasions declined as species
richness was reduced in experimental plots (Naeem et al. 1994, Tilman et al.
1997, Hector et al. 1999).
However, since high and low richness plots had different species compositions,
it was not easy to differentiate between the "sampling effect", i.e. having
high
productivity because there was a greater probability of selecting productive
species in high richness plots, and complementarity effects that are based on
more
efficient resource use by a complement of species. Since 1997, we have been
experimentally
varying the other component of diversity, evenness, in experimental grassland
plots. By varying evenness instead of richness, plots with different levels of
diversity are created, but without the variability caused by different species
compositions. In the first experiment, which was done in an old field, we
found that total primary productivity decreased linearly as community
diversity (evenness) was reduced, and that it was largely invariant to changes
in species
composition. (Wilsey and Potvin
2000). A second experiment found that communities with lowered evenness
were less resistant to invasion by plants and spittle bugs (Wilsey and Polley
2002). In more recent experiments, we found that species richness and evenness
have additive effects on primary productivity and ecosystem C exchange (Wilsey
and Polley 2004), and that invasion resistance (Losure et al. 2007) and NPP
(Isbell et al. 2008) can vary
between extinction scenarios in prairie communities. Species that green-up
early
in the growing season were especially important in preventing invasion because
their growth period matched the period of maximum invasion pressure (Losure et
al. 2007).
Species diversity partioning
What should we be measuring in biodiversity studies? Are species abundances
related to local extinction risk? Do changes in rarity (quantified with
evenness measures) occur before local extinctions? Under what conditions is
seed limitation important and how do they alter diversity components? Species
diversity has
multiple components, and we are attempting to develop a
better understanding of how components are related and whether they respond
similarly to ecological processes. We have found that a diversity partitioning
approach provides us with a more complete understanding of diversity compared
to using single measures alone. Studies have looked at
relationships between richness, evenness (inverse of dominance), and
heterogeneity measures (Stirling
and Wilsey 2001, Wilsey et al. 2005b) and between local (alpha) and regional
scale (beta) measures (Martin et al. 2005, Wilsey 2009). We have looked at
relationships
between evenness and richness in a literature survey (Stirling and Wilsey
2001) and with across-grassland data (Wilsey et al. 2005b) at the local scale.
Surprisingly, we
found that richness and evenness can be negatively correlated in plant
communities (Stirling and Wilsey 2001, Wilsey et al. 2005b), and that evenness
accounts for much more of the variation in plant diversity (H') than does
richness (Stirling and Wilsey
2001).
Evidence from plant communities suggested that evenness and richness are acting
as diversity components (Stirling and Wilsey 2001) each responding in their own
way to changes in the environment, with richness responding
more to migration during seed dispersal events and evenness responding more to
competition intensity and ungulate grazing (Martin and Wilsey 2006, Wilsey
and Stirling 2007). Changes in evenness often precede (and predict) changes in
richness (Wilsey and Polley 2004, Wilsey and Stirling 2007, Wilsey et al.
2009). Thus, species richness alone seems to be an incomplete
indicator of diversity
in plant communities, and studies of both dimensions of diversity (evenness and
richness) can be more informative than studies with richness alone. Current
research is
testing various mechanisms of biodiversity maintenance in native vs. exotic
communities (Wilsey et al. 2009).
Past Interests:
In the past, we studied how herbivores affect plant responses to
changes in the environment; for example, are responses to global change larger
or smaller in
areas where plants are defoliated by herbivores? In studies that grew grasses
under both elevated and ambient
levels of atmospheric CO2, we found that defoliation had little
affect on the response of many species to elevated CO2 >(Wilsey et
al.
1997), but that in some species, defoliation
led to a smaller increase in growth under elevated CO2 (Wilsey
1996, 2001).
Another study found that patches in tropical pastures that had been grazed by
cattle had lower
ecosystem respiration and net CO2 release than did ungrazed patches
(Wilsey et al. 2002).
Selected Current and Past Projects
- MEND:
Maintenance of Exotic vs. Native Diversity
-
Effects of Dominant Species on Loess Hill Prairie Restorations
- Grazing
Effects on Plant and Ecosystem Processes
- Quantifying
Prairie Restoration Success
GRADUATE STUDENTS AND POSTDOCS
Leanne Martin, M.S. May 2005, Ph.D. student
David Losure, M.S., May 2006
Andrea Blong, M.S., May 2007
Kathryn Yurkonis, Ph.D. candidate
Forest Isbell, Ph.D. candidate
Tim Dickson, Postdoc
Pedram Daneshgar, Postdoc
SELECTED RECENT PUBLICATIONS AND DATASETS FROM THE WILSEY LAB:(Complete List).
-
Wilsey, B.J. 2009. An empirical comparison of beta diversity indices in
establishing prairies. Ecology
in press
-
Wilsey, B.J., Teaschner, T.B., Daneshgar, P.P., Isbell, F.I. and H.W. Polley.
2009. Biodiversity maintenance mechanisms differ between native and novel
exotic-dominated communities. Ecology Letters
12:432-442
-
Isbell, F.I., Polley, H.W. and B.J. Wilsey. 2009. Species interaction
mechanisms maintain grassland plant species diversity.Ecology
90:1821-1830
-
Dickson, T.L. and B.J. Wilsey. 2009. Biodiversity and tallgrass prairie
decomposition: the relative importance of species identity, evenness, richness
and microtopography.Plant Ecology201:639-649
-
Dickson, T.L., Wilsey, B.J., Busby, R.R. and D.L. Gebhart. 2009. A non-native
legume causes large community and ecosystem changes in both the presence and
absence of a cover crop. Biological Invasionsin press
-
Yurkonis, K.A., B.J. Wilsey, K.E. Moloney, and A. van der Valk. 2009. Paired
drilled and broadcast grassland reconstructions have similar diversity but
differ in dominant plant distributions. Restoration Ecology in press
-
Wilsey, B.J. 2009. Productivity and subordinate species response to dominant
grass species and seed source during restoration.Restoration Ecology
in press
-
Isbell, F.I., Losure, D.A., Yurkonis, K.A. and B.J. Wilsey. 2008. Diversity-
productivity relationships in two realistic rarity-extinction
scenarios.Oikos.
117:996-1005
-
Losure, D.A., Wilsey, B.J. and K.A. Moloney. 2007. Evenness-invasibility
relationships differ between two extinction scenarios in tallgrass
prairie. Oikos.
116:87-98.
[PDF]
-
Wilsey, B. and G. Stirling. 2007. Species richness and evenness respond in a
different manner to propabule density in developing prairie microcosm
communities. Plant Ecology.
190:259-273.
[PDF]
-
Polley, H.W., Wilsey, B.J. and J.D. Derner. 2007. Dominant species constrain
effects of species diversity on temporal variability in biomass production of
tallgrass prairie. Oikos.
116:2044-2052.
[PDF]
-
Wilsey, B.J. and H.W. Polley. 2006.
Aboveground productivity and root-shoot allocation differ between native and
introduced grass species. Oecologia.
150:300-309.
[PDF]
-
Martin, L.M. and B.J. Wilsey. 2006. Assessing grassland restoration success:
relative roles of seed additions and native ungulate activities. Journal of
Applied Ecology
43:1098-1110.
[PDF]
-
Wilsey, B.J. Martin, L.M. and H.W. Polley. 2005a.
Predicting plant extinction based on species-area curves in prairie fragments
with high beta richness. Conservation Biology.
19:1835-1841.
[PDF][Dataset][Appendix]
-
Wilsey, B.J. Chalcraft, D.R., Bowles, C.M., and M.R. Willig. 2005b.
Relationships among indices suggest that richness is an incomplete surrogate
for grassland biodiversity. Ecology
86:1178-1184.
[PDF]
-
Martin, L.M., Moloney, K.A. and B.J. Wilsey. 2005. An assessment of grassland
restoration success using species diversity components. J. Applied Ecology
42:327-336.
[PDF]
-
Wilsey, B.J. and H.W. Polley. 2004. Realistically low species evenness does
not alter grassland species-richness-productivity relationships. Ecology
85:2693-2700.[PDF]
-
Wilsey, B.J. and H.W. Polley. 2003. Effects of seed additions and grazing
history on species diversity and aboveground productivity of sub-humid Texas
grasslands. Ecology 84:920-932.[PDF]
- Wilsey, B.J. and H.W. Polley. 2002. Reductions in grassland species
evenness increase dicot seedling invasion and spittle bug infestation.
Ecology
Letters 5:676-684.[PDF]
- Wilsey, B.J., Parent, G., Roulet, N.T., Moore, T.R., and C. Potvin. 2002.
Tropical pasture carbon cycling: relationships between C source/sink strength,
aboveground biomass, and grazing. Ecology Letters 5:367-376.[PDF]
- Stirling, G. and B. Wilsey. 2001. Empirical relationships between
species
richness, evenness and proportional diversity.
American Naturalist 158:286-300.[PDF]
- Wilsey, B.J. and C. Potvin. 2000. Biodiversity and ecosystem functioning:
the importance of species evenness in an old field. Ecology
81(4):887-892 Abstract
Date Last Modified: June 2, 2009
Copyright 2000 Brian J Wilsey