My
research program is aimed at achieving a deeper, mechanistic
understanding of basic ecological and evolutionary processes.
I aim to better understand
the general underlying “rules of nature” that control the survival,
growth, and reproduction in individual organisms, and then use these rules
to make predictions about the structure and function of communities and ecosystems.
To do so, I work in broad collaboration with scientists from many disciplines
to develop simple, quantitative models, based on first principles, and then
rigorously
test
these models with data from field or laboratory studies. I work in both
terrestrial
and aquatic ecosystems with a variety of different organisms. In fact, much
of my research combines data from different organisms and ecosystems, often
at broad spatial or temporal scales (i.e., macroecology). In the coming years,
I wish to use a combination of experimental, theoretical and field-based
approaches to address questions. This research helps to link species to
ecosystems,
genes to phenotypes, and also ecology to evolution. It has implications for
current environmental problems such as global climate change. Three current
focus areas of research are described below:
Controls on Individual Metabolism: This research focuses
on how first principles of physics, chemistry and biology combine to constrain
the physiology or life history of organisms. In particular,
I focus on how the effects of body size, temperature, and resource supply
constrain basic rate processes in individuals,
particularly metabolic rate (B). This research falls under the heading of
physiological ecology. For
example, my colleagues and I have shown how the combined effects of body
size and temperature explains
much of the variation in metabolic rate for various taxonomic groups ranging
from plants, to animals and microbes (Gillooly
et al. 2001)(see Figure).
Since metabolic rate controls many other biological rates and times, the
simple equation describing the size and temperature-dependence of metabolic
rate,
, can be used to predict
many other biological rates and times in individuals, including hatching
rates and lifespans (Gillooly
et al. 2002).
This research has implications at all levels of biological organization and
is the basis of our “metabolic theory of ecology” (Brown
et al. 2004).
Linking Ecosystem Processes to Individual Metabolism: This
research focuses on linking the nutrient cycling of carbon, phosphorus and
nitrogen in whole ecosystems to the flux, storage and turnover of these important
nutrients in
individuals. In other words, this research aims to link species to ecosystems.
By combining our metabolic framework with that of ecological
stoichiometry, I aim to quantify the contribution of biota to biogeochemical
cycles. For example, recent research by our group has shown that we can
predict the concentration of RNA and phosphorus at the individual-level
using this
approach(Gillooly et al. 2005a).
We also can predict many aspects of the global carbon cycle such as turnover
rate (see
Figure)(Allen et al. 2005). In
the future, this research could have important implications for understanding
the
response of ecosystems to global change.
Linking Evolutionary Dynamics and Patterns of Biodiversity to Individual
Metabolism: This research focuses on predicting rates of evolution
based on rates of energy flux (i.e., metabolic rate) occurring in individuals.
Specifically, this research first aims to develop models that predict rates
of molecular evolution, and rates of speciation and extinction, based on
the size and temperature-dependence of individual metabolic rate. I then
aim to address how such evolutionary dynamics may contribute to patterns
in biodiversity. For example, recent research by our group has shown that
a metabolic approach can predict rates of neutral molecular evolution (Gillooly
et al. 2005b). This research helps in understanding the origin and
maintenance of biodiversity (Allen et al.
2002).
It will involve both theoretical work and a series of laboratory experiments.
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