I use this "gallery" as a place to post talks that I have given.
Establishment and spread in the face of uncertainty:
When a population arrives in a novel environment (e.g. pathogen arriving in a new host species, a species transported to a novel habitat), demographic stochasticity and environmental heterogeneity may determine whether the population successfully establishes and, upon establishment, the rate at which is spreads across the landscape. This talk at University of Chicago (Feb. 25, 2013) attempts to synthesize some of my work in the past few years on the question of establishment and spread in the presence of demographic or environmental stochasticity.
Metastability: all
populations eventually go extinct. However, the time to extinction
may be exceptionally long and be preceeded by transient dynamics
that exhibit a regular statistical pattern. For stochastic models in
population biology, these duration of these transients often depends
on size of the system (e.g. the carrying capacity of a population).
For example, the above figure compares and constrasts the stochastic
dynamics (in red) and the mean field dynamics (in black) of a
host-parasitoid model; lower subfigures correspond to higher host
carrying capacities. These figures suggest that as the system size increases, the
attractors of the mean field model (a period four orbit) should provide a good description
of the metastable behavior of the stochastic model. In collaboration
with Mathieu Faure, we have proven tha this correspondence holds
for a general class of Markov chains. Furthermore, we provide
estimates of how time to extinction time scales with system system size. Here is a somewhat technical talk that I gave at
Berkeley's Analysis and PDE seminar (Nov. 19th, 2012) on this
topic. You can read about the nitty gritty mathematical details here. .
Eco-evo feedbacks:
Ecological communities consist of complex webs of interacting
species, each of which contain phenotypically diverse
individuals. Species interactions drive ecological dynamics, while
the genetic variation within species provides the raw material for
natural selection. While ecological and evolutionary processes were
traditionally not studied together, there is mounting evidence that
feedbacks between the ecological and evolutionary processes (eco-evo
feedbacks) occur over commensurate time scales (e.g. tens to
thousands of generations instead of hundreds of thousands of
generations). This raises the possibility that one can not be
considered without the other.
Dan Bolnick, Reinhard Burger and I studied these feedbacks for
species sharing a predator with phenotypic variation in its ability
to attack either prey species. Here is talk that I gave about some of our results
at ESA in 2011.
Hedging your
bets: All populations experience variability in environmental
conditions (e.g. temperature, percipitation) across time or
space. Since these environmental conditions influnence the
propensity to survive, grow, and reproduce, populations can hedge
their bets by distributing individuals across time and
space. Understanding the evolution of these bet-hedging strategies
and their ecological consequences continues to be one of the focii
of my research. Here is a talk that I
gave to students at the US Naval Academy (Nov. 27, 2012) introducing
them to the world of bet-hedging. Some of my contributions to
this theory include evolution of patch selection
in stochastic environments, stochastic growth rates of
populations in spatially and temporally variable environments,
and upcoming work on the evolution of reproductive strategies of
plants experiencing pollen variability.