|
Adelaide Rhodes, Ph.D., Postdoctoral Research Associate
![]()
I have spent the past nine years developing practical
culture systems for marine copepods to be used in the study of early larval
fish development. The reliable laboratory culture of copepods has allowed me to
test hypotheses on trophic uptake and bioconversion of lipids by marine
organisms; fish growth and development; larval fish behavior; predator-prey
interactions; etc. While I am mainly
interested in fatty acids, my research interest in copepods has expanded to
include ecological processes, invasive species, and functional genomic
regulation of lipid storage. Copepods hold the key to the successful recruitment and/or aquaculture of many important commercial and ornamental species.
|
||
|
Education
2004 Ph.D. Zoology, North Carolina State University, Raleigh, NC
1992 M.S. Oceanography, Florida Institute of Technology, Melbourne,FL 1990 B.A. Physics, University of Virginia, Charlottesville, VA Dissertation Research
As a doctoral student, my research focused
on elucidating the lipid and carotenoid bioconversion capabilities of marine
harpacticoid copepods. I conducted basic
experiments that varied the diets of the model organism Nitokra lacustris. I
measured the differences in population growth rates, lipid content and lipid
quality. I created a model that
predicted population growth rates based on observation of individual life
history parameters and validated the model with a series of large-scale
(>100 L) culture experiments in a fish hatchery. In order to complete this work, I created
novel methods for the growth and maintenance of harpacticoid copepods
species. In fact, I still have the
original culture of Nitokra lacustris,
started in 1998, sitting on my kitchen counter.
Recent Accomplishments
In my postdoctoral research experience at the Northwest
Fisheries Science Center in Seattle, Washington, I designed and carried out
fish feeding experiments on larval and juvenile coldwater marine species (rock
sole, rockfish, Pacific cod, etc.). I
used a variety of live and inert feeds to investigate the transfer of nutrients
from zooplankton to ichthyoplankton utilizing several methods: HPLC, GC, and inert markers (ICP). At the
Northwest Fisheries Science Center, I recently completed two projects on fish
growth and nutrient utilization, which are being prepared for publication: 1.) protein replacement diets for lingcod Ophiodon elongatus utilizing Alaskan
fisheries by-product and by-catch meals, and 2.) a rapid method to measure the
relative uptake of live prey and inert feeds fed to larval finfish.
|
||
|
Recent Classes
Spring, 2008: BIO 490E (ECO 486B, University of Washington, Seattle
"The Future of Our Planet: Climate, Ecosystems, and Society." Co-instructors: Susan Bates (Atmospheric Sciences); Lisa Marin (Biology) - 2 credit seminar Spring 2007: TESC 408, University of Washington, Tacoma (sole instructor) "Marine Plankton" - 6 credit lecture/lab Awards and Honors
2008 Future Faculty Fellows, University of Washington, Teaching Apprenticeship: "The Future of Our Planet: Climate, Ecosystems and Society" 2007 University of Washington Postdoctoral Research Symposium Speaker 2005 Plenary Speaker, World Association of Copepodologists Section on the Role of Copepods in Aquaculture, 9th ICOC 2002 1st Place Student Poster Award, World Aquaculture Society 2001 Starr Fellowship, Bermuda Biological Station for Research 2000 University Alumni Fellowship, North Carolina State University 2000 Aylesworth Scholarship, Florida Sea Grant 1996 Dean John A. Knauss Marine Policy Fellowship, National Sea Grant, NOAA1992 Aylesworth Scholarship, Florida Sea Grant 1992 Citizens Environmental Appreciation Award, Indian River Lagoon National Estuary Program |
Genomics Research (2007-2008)
I have recently started to incorporate a functional and
comparative genetic approach to my research on larval fish development and
copepod biology. I feel that this
approach can provide valuable information on basic physiological processes,
such as digestive enzyme development in marine fish and lipid storage in marine
copepods. Once these physiological
processes have been characterized in the species of interest, I will be able to
measure organismal responses to environmental stressors such as reduced prey
availability, ocean acidification, the presence of endocrine disruptors and
other forms of pollution. By monitoring
the expression levels of select genes in laboratory cultures of copepods and/or
fish larvae subjected to abiotic and biotic stresses such as toxic algal
species and temperatures outside the optimum range we could predict the impacts
to the food chain from these possible threats to ecosystem health. Aquaculture (2006-2007)
One project tested the efficacy of utilizing Alaskan fisheries by-product and by-catch meals as part of larval and juvenile fish diets. The second project analyzed the uptake of various prey items through the trophic food chain utilizing a variety of live feeds fed inert metal oxides and then fed to larval finfish. During my time at NOAA Fisheries, I also worked on constructing a functional hatchery scale copepod production system to produce millions of copepods per day for research and analysis of the transfer of nutrients. We are awaiting further funding to complete and field test this pilot system. Ballast Water Research Team (2005-2006)
In my first year as a postdoctoral researcher at UW, I assisted the Ballast Water Research Team under the supervision of Russell Herwig and Jeff Cordell at the University of Washington. My role in the team was to provide and maintain cultures of nearly forty species of freshwater and marine zooplankton, many of them started from field samples. These cultures were utilized in a range of tests designed to improve the Environmental Technology Verification (ETV) process. The ETV process screens promising new technologies for the reduction of non-indigenous species introduction through ballast water exchange. After culturing and screening the microzooplankton species, we developed a short list of seven surrogate organisms that could potentially be used to represent the response of a much broader group of organisms. We then developed and conducted ecotoxicological assays for microzooplankton using ten proposed ballast water treatment technologies (e.g. ozone, UV, several biocides). After screening, I collected the data from the hundreds of experiments conducted by our lab and our collaborators at Woods Hole, West Virginia University and Old Dominion and prepared a comprehensive database tool for comparing and analyzing the effectiveness of proposed treatments for ridding ballast tanks of bacteria, phytoplankton, protists and zooplankton. The database results were presented to representatives from the EPA, NOAA, and U.S. Coast Guard at a scientific panel meeting in 2007. The U.S. Coast Guard and the Smithsonian Environmental Research Center will make this database tool available to researchers around the world as part of the National Ballast Information Clearing House (NBIC). Other Collaborative Research Activities
Due to my expertise with culturing and maintaining
phytoplankton and zooplankton cultures, I often help local colleagues develop
and implement experiments involving zooplankton. For example, working with colleagues from the
Department of Oceanography at UW, Dr. Anitra Ingalls and Dr. Carme Huguet, I
will be assisting in a study of how copepod ingestion of Crenarchaeota may impact lipid biomarkers. Crenarchaeota lipid biomarkers are used to determine the change in
surface water temperatures over time, and it is possible that the encapsulation
of Crenarchaeota in calanoid faecal
pellets may alter the lipid biomarkers.
This experiment will involve field sampling of zooplankton that reside
in the water column alongside the Crenarchaeota
as well as laboratory experiments to measure the key lipid biomarkers in
copepod faecal pellets. In another interesting experimental system, I will be using
radiolabeled liposomes to measure the omega-3 bioconversion capability of
freshwater and marine zooplankton. I am
collaborating with Dr. Michael Brett in the Department of Civil &
Environmental Engineering at the UW on this project, and we are awaiting
notification of funding to continue the work.
If successful, we will be able to trace the bioconversion of 18:3n3 to the essential fatty acids
eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) by lower trophic
levels food in freshwater and marine systems.
For the freshwater system, we will track lipid bioaccumulation and/or
bioconversion by the calanoid copepod Diaptomus
ashlandi fed to a freshwater model fish species Tilapia nilotica. In the
marine system, we hope to replicate the experiment using Acartia tsuensis, a local calanoid, fed to larval rockfish (Sebastes sp.). |
Selected Publications
Rhodes, A. 2007. Dietary effects on carotenoid composition in
the marine harpacticoid copepod Nitokra
lacustris. Journal of Plankton Research 29(Supplement 1):i73-i83. Rhodes, A. and L. Boyd. 2005. Formulated feeds for harpacticoid copepods: Implications for population growth and fatty acid composition. In: C.S. Lee, P. J. O'Bryen and N. H. Marcus (Eds.) Copepods in Aquaculture, Blackwell Publishing, Oxford, UK, pp. 61-73. ISBN 0-8138-0066-8 Rhodes, A. 2003. Methods for mass culture of Nitokra lacustris, a marine harpacticoid copepod. In: H.I. Browman and A.B. Skiftesvik (Eds.). The Big Fish Bang. Proceedings of the 26th Annual Larval Fish Conference. Institute of Marine Research, Bergen, Norway, pp: 449-465. ISBN 82-7461-059-8 Rhodes, A. 2004. Marine Harpacticoid Copepod Culture for the Production of Long Chain Highly Unsaturated Fatty Acids and Carotenoid Pigments. Ph.D. Dissertation, North Carolina State University, 161 pp. |
|
Send mail to: acer@u.washington.edu
Last modified: 11/23/2007 1:05 PM |
||