Growth rates, grazing, sinking, and iron limitation of equatorial Pacific phytoplankton

Concentrations of phytoplankton and NO{sub 3} are consistently low and high in surface waters of the oceanic eastern and central equatorial Pacific, and phytoplankton populations are dominated by small solitary phytoplankton. Growth rates of natural phytoplankton populations, needed to assess the relative importance of many of the processes considered in the equatorial Pacific, were estimated by several methods. The growth rates of natural phytoplankton populations were found to be {approximately}0.7 d{sup {minus}1} or 1 biomass doubling d{sup {minus}1} and were similar for all methods. To keep this system in its observed balance requires that loss rates approximate observed growth rates. Grazing rates, measured with a dilution grazing experiment, were high, accounting for a large fraction of the daily production. Additions of various forms of Fe to 5-7-d incubations utilizing ultraclean techniques resulted in significant shifts in autotrophic and heterotrophic assemblages between initial samples, controls, and Fe enrichments, which were presumably due to Fe, grazing by both protistan and metazoan components, and incubation artifacts. Estimated growth rates of small pennate diatoms showed increases in Fe enrichments with respect to controls. The growth rates of the pennate diatoms were similar to those estimated for the larger size fraction of the natural populations.

[1]  Francisco P. Chavez,et al.  Standing stocks of particulate carbon and nitrogen in the equatorial Pacific at 150°W , 1992 .

[2]  F. Morel,et al.  Limitation of productivity by trace metals in the sea , 1991 .

[3]  K. Coale,et al.  Effects of iron, manganese, copper, and zinc enrichments on productivity and biomass in the subarctic Pacific , 1991 .

[4]  S. Fitzwater,et al.  The case for iron , 1991 .

[5]  Thomas M. Powell,et al.  Ecological dynamics in the subarctic Pacific, a possibly iron-limited ecosystem , 1991 .

[6]  H. D. Baar,et al.  Metal enrichment experiments in the Weddell-Scotia Seas: Effects of iron and manganese on various plankton communities , 1991 .

[7]  A. Gargett Physical processes and the maintenance of nutrient‐rich euphotic zones , 1991 .

[8]  Francisco P. Chavez,et al.  Phytoplankton taxa in relation to primary production in the equatorial Pacific , 1990 .

[9]  H. Marchant,et al.  Kakoeca antarctica gen. et sp.n., a loricate choanoflagellate (Acanthoecidae, Choanoflagellida) from Antarctic sea ice with a unique protoplast suspensory membrane , 1990 .

[10]  D. M. Nelson,et al.  Phytoplankton growth and new production in the Weddell Sea marginal ice zone in the austral spring and autumn , 1990 .

[11]  R. Olson,et al.  Spatial and temporal distributions of prochlorophyte picoplankton in the North Atlantic Ocean , 1990 .

[12]  F. Morel,et al.  Availability of well-defined iron colloids to the marine diatom Thalassiosira weissflogii , 1990 .

[13]  R. Gordon,et al.  Yes, it does: A reply to the comment by Banse , 1990 .

[14]  K. Banse Does iron really limit phytoplankton production in the offshore subarctic Pacific , 1990 .

[15]  W. Broecker Comment on “Iron deficiency limits phytoplankton growth in Antarctic waters” by John H. Martin et al. , 1990 .

[16]  John H. Martin glacial-interglacial Co2 change : the iron hypothesis , 1990 .

[17]  W. G. Harrison,et al.  Primary productivity and size structure of phytoplankton biomass on a transect of the equator at 135°W in the Pacific Ocean , 1990 .

[18]  D. Vaulot,et al.  A simple method to preserve oceanic phytoplankton for flow cytometric analyses. , 1989, Cytometry.

[19]  W. Broenkow,et al.  Vertex: phytoplankton/iron studies in the Gulf of Alaska , 1989 .

[20]  F. Chavez Size Distribution of phytoplankton in the central and eastern tropical Pacific , 1989 .

[21]  Sallie W. Chisholm,et al.  A novel free-living prochlorophyte abundant in the oceanic euphotic zone , 1988, Nature.

[22]  F. Chavez,et al.  An estimate of new production in the equatorial Pacific , 1987 .

[23]  E. Laws,et al.  High phytoplankton growth and production rates in the North Pacific subtropical gyre1,2 , 1987 .

[24]  E. Stoermer,et al.  Estim.ation of intracellular carbon and silica content of diatoms from natural assemblages using morphometric techniques , 1984 .

[25]  J. Waterbury,et al.  Biochemical composition and short term nutrient incorporation patterns in a unicellular marine cyanobacterium,Synechococcus(WH7803)1 , 1984 .

[26]  S. Fowler,et al.  Dissolved and fecal pellet carbon and nitrogen release by zooplankton in tropical waters , 1983 .

[27]  S. Fitzwater,et al.  Metal contamination and its effect on primary production measurements1 , 1982 .

[28]  A. T. Chan COMPARATIVE PHYSIOLOGICAL STUDY OF MARINE DIATOMS AND DINOFLAGELLATES IN RELATION TO IRRADIANCE AND CELL SIZE. II. RELATIONSHIP BETWEEN PHOTOSYNTHESIS, GROWTH, AND CARBON/CHLOROPHYLL a RATIO 1, 2 , 1980 .

[29]  Roger Desrosières SURFACE MACROPHYTOPLANKTON OF THE PACIFIC OCEAN ALONG THE EQUATOR , 1969 .

[30]  P. R. Sloan,et al.  RELATIONSHIP BETWEEN CARBON CONTENT, CELL VOLUME, AND AREA IN PHYTOPLANKTON , 1966 .

[31]  C. Lorenzen,et al.  Fluorometric Determination of Chlorophyll , 1965 .

[32]  M. Silver,et al.  The “particle” flux: Origins and biological components , 1991 .

[33]  F. Chavez,et al.  The Galápagos Islands and Their Relation to Oceanographic Processes in the Tropical Pacific , 1991 .

[34]  F. Wilkerson,et al.  Regional perspectives in global new production , 1989 .

[35]  B. Prézelin,et al.  Pico- and ultraplankton Sargasso Sea communities: variability and comparative distributions of Synechococcus spp. and algae , 1988 .

[36]  S. El-Sayed,et al.  Contributions of the net, nano- and picoplankton to the phytoplankton standing crop and primary productivity in the Southern Ocean , 1987 .

[37]  J. Waterbury,et al.  Biological and ecological characterization of the marine unicellular Cyanobacterium Synechococcus , 1987 .

[38]  B. Frost,et al.  Grazing control of phytoplankton stock in the open subarctic Pacific Ocean: a model assessing the role of mesozooplankton, particularly the large calanoid copepods Neocalanus spp. , 1987 .

[39]  B. C. Booth The Use of Autofluorescence for Analyzing Oceanic Phytoplankton Communities , 1987 .

[40]  F. Chavez,et al.  Ocean variability in relation to living resources during the 1982–83 El Niño , 1986, Nature.

[41]  F. Azam,et al.  Toxic effects of latex and Tygon tubing on marine phytoplankton, zooplankton and bacteria , 1986 .

[42]  Thomas L. Hayward,et al.  DETERMINING CHLOROPHYLL ON THE 1984 CALCOFI SURVEYS , 1984 .

[43]  M. Elbrächter,et al.  On the Ecological Significance of Thalassiosira partheneia in the Northwest African Upwelling Area , 1978 .

[44]  John J. Walsh,et al.  Herbivory as a factor in patterns of nutrient utilization in the sea1 , 1976 .

[45]  J. Ryther,et al.  Organic chelators: Factors affecting primary production in the cromwell current upwelling☆ , 1969 .

[46]  G. Hasle A quantitative study of phytoplankton from the equatorial Pacific , 1959 .