Robert A. Armstrong
Associate Professor
Ph.D., 1975, University of Minnesota
rarmstrong@notes.cc.sunysb.edu

Mathematical modeling in marine ecology
and biogeochemistry.


Research Interests (Global Research)

My specialty is the mathematical modeling of ecological, physiological, and biogeochemical processes, and the application of these models to understanding and prediction in marine sciences.  My goal is to translate qualitative ideas and data into the minimal amount of mathematics that will allow adequate representation of mechanism, then to confront the resulting models with data.

My current research addresses several specific issues.  First, I have been modeling deep-water fluxes of organic carbon and the associated fluxes of "ballast" minerals (silicate and carbonate minerals, and dust).  Work with several collaborators has shown that deep-water carbon fluxes may be more accurately predicted from mineral ballast fluxes than from surface production of organic carbon, challenging an existing scientific bias towards marine photosynthesis as the dominant process determining the marine carbon cycle.  The empirical component of these studies is centered on the French DYFAMED site off Nice and Monaco, in the Mediterranean Sea.

This biogeochemical work is intimately tied to a second major interest: the structure of oceanic food webs.  If, as suggested by the carbon flux study described above, deep-ocean carbon fluxes may be more directly related to mineral production than to surface carbon production, then predicting the taxonomic structure of plankton communities becomes of critical importance: within the phytoplankton, diatoms, coccolithophorids, and prochlorophytes may have different consequences for the sinking of carbon; and within zooplankton, little-studied groups such as radiolarians, foraminifera, and pteropods may be critical components of the ocean carbon cycle.

Finally, modeling of food chains must be based on reliable models of phytoplankton physiology, since food chain effects are assessed as residuals after growth has been subtracted. Here I have developed new models of phytoplankton physiology that reflect processes missed by earlier models, but whose representation is crucial if food chain effects are to be properly evaluated.

Most Relevant Publications:

Armstrong, R.A. Nitrogen allocation and photoacclimation in the Geider et al. (1998) model of photosynthesis: alternative representations based on optimality. Deep-Sea Research II (in review)

Armstrong, R.A. 2003.  Representing size structure and biogeochemical diversity in ecosystem models of the ocean carbon cycle.  pp. 254-271  In The role of models in ecosystem science, C.D. Canham, J.J. Cole, and W.K. Lauenroth, eds. Princeton University Press, Princeton, NJ, USA.

Armstrong, R.A. 2003.  A hybrid spectral representation of phytoplankton growth and zooplankton response: The "control rod" model of plankton interaction.  Deep-Sea Research II 50:2895-2916.

Armstrong, R.A., C. Lee, J.I. Hedges, S. Honjo, and S.G. Wakeham.  2002. A new, mechanistic model for organic carbon fluxes in the ocean, based on the quantitative association of POC with ballast minerals.  Deep-Sea Research II 49:219-236.

Armstrong, R.A. 1999. Stable model structures for representing biogeochemical diversity and size spectra in plankton communities. J. Plankton Res. 21:445-464.

Armstrong, R.A. 1999. An optimization-based model of iron-light-ammonium colimitation of nitrate uptake and phytoplankton growth. Limnol. Oceanogr. 44:1436-1446.

Armstrong, R.A., and R. McGehee. 1980. Competitive exclusion. Amer. Nat. 115:151-170.

 

Page last modified on Thursday, September 29, 2005 by George E. Carroll