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SEMINAR: MBF602 STUDENT SEMINAR: TODAY @ 1PM---ANDREW KOUGH & ANDREW KEMPSELL
| From: | Pam Harris <pharris@rsmas.miami.edu> |
| Subject: | SEMINAR: MBF602 STUDENT SEMINAR: TODAY @ 1PM---ANDREW KOUGH & ANDREW KEMPSELL |
| Date: | Fri, 18 Nov 2011 09:46:40 -0500 |
|
MBF Student Seminar
Series
Andrew Kough Advisor:
Dr. Claire Paris “Lessons from the Larval
Connectivity of Caribbean Spiny
Lobsters” The oceanic dispersal of the planktonic larvae that connect disjunct marine animal populations remains an enduring mystery, complicating the management of species that support valuable fisheries, especially since larvae recognize no international boundaries. While revolutionary techniques such as stable isotopic tagging and parentage analysis have been proven effective at identifying small scale demographic connectivity patterns in reef fish, they are financially and logistically impractical on fishery relevant scales and unproven with invertebrates. A commonly applied alternative technique is coupled-biophysical modeling. This study focuses on the larval transport of the spiny lobster, Panulirus argus, as a representative species with a rich history of scientific inquiry, commercial worth exceeding 1B$USD, and cultural value firmly entrenched in many different countries. The goal is to reveal the sources, sinks, and routes connecting the Caribbean metapopulation; synthesizing empirical data from laboratory studies, mail surveys, and previously published works to parameterize an individual based model of lobster larval connectivity. Results were then evaluated using two independent sites, separated by over 500 miles, giving staunch support to the model’s performance - something never before achieved for spiny lobster or any other larvae at such large spatio-temporal scales. This sets a precedent for future explorations into wide-scale larval dispersal, demonstrating a successful union of empirical research and probabilistic modeling. Andrew Kempsell
D-Aspartate
(D-Asp)
may be a novel neurotransmitter in the Aplysia nervous system.
Previous
studies have led to the proposal that D-Asp is an alternate
agonist at
ionotropic glutamate (L-Glu) receptor-channels (L-Glu
receptors), specifically
at N-methyl-D-Aspartate (NMDA) receptors, which are calcium
channels with a
role in both vertebrate and invertebrate learning and memory.
Pharmacological
differences were documented between D-Asp- and L-Glu-activated
currents in whole
cell voltage clamp studies in buccal S cluster neurons.
Kynurenate, a general
L-Glu receptor antagonist, blocked D-Asp whole cell current
amplitude
significantly by 27±19%.
In
the same cells, kynurenate blocked a significantly greater
proportion (65±13%)
of
L-Glu-elicited currents, suggesting that the two agonists bind,
in part, at
different sites. PPDA, a subunit-specific NMDA receptor blocker,
significantly
reduced D-Asp and L-Glu currents by 46±22%
and 46±11%, respectively,
suggesting that ~46% binding of D-Asp and L-Glu is
pharmacologically similar
and might represent an NMDA-like receptor activated by these
agonists. APV, a
known NMDA receptor antagonist in vertebrates, blocked a small
but significant
percentage of D-Asp currents, but did not block L-Glu currents.
Together, these
findings suggest that D-Asp and L-Glu receptors share some
binding sites but
that there may be a unique D-Asp receptor not distinguishable
with pharmacological
tools. Friday, November 18, 2011 1:00pm RSMAS
campus,
S/A 103 Pamela
Harris
Administrative Assistant Marine Biology and Fisheries Rosenstiel School of Marine and Atmospheric Science University of Miami 4600 Rickenbacker Causeway/SLAB-118 Miami, FL 33149 (305) 421-4176 fax - (305) 421-4600 pharris@rsmas.miami.edu http://www.rsmas.miami.edu/academics/divisions/marine-biology-fisheries/ |
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- From: Pam Harris <pharris@rsmas.miami.edu>
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