Skip to main content
Log in

Primary productivity and phytoplankton size fraction dominance in a temperate North Atlantic estuary

  • Published:
Estuaries Aims and scope Submit manuscript

Abstract

The composition, productivity, and standing crop of net (>20 μm) and nano-(<20 μm) phytoplankton of Peconic Bay, Long Island, New York was examined from June 1978 through May 1979. Nanoplankton, primarily small solitary flagellates, chlorophytes, and diatoms, dominated from May through September accounting for 88.5% of the productivity and 88.1% of the standing crop (measured as chlorophyll a). An apparent net plankton bloom began in December and continued through March. The dominant organism through most of the winter bloom was the chain-forming diatom Skeletonema costatum (Grev.) Cl. Net plankton at this time represented 66.4% of the standing crop. For both size fractions, productivity/chlorophyll a (g C per g chl a per d, integrated through the euphotic zone) was a function of light energy over the year with the exception of a few sampling dates during the post-winter bloom period. Assimilation numbers (g C per g chl a per h at saturating light intensities) were a function of temperature between 0 and 20°C. Nitrogen deficiency did not appear to be a factor in regulating phytoplankton growth rate through the euphotic zone, as ratios of 14C assimilation for dark bottles enriched with NH3 and with no enrichment exhibited no relationship to environmental dissolved inorganic nitrogen concentrations. Zooplankton grazing pressure appeared to have been an important factor in regulating the upper limit of phytoplankton biomass and in influencing size fraction dominance. Dominance of one phytoplankton size fraction over the other on any given date was not based on physiological differences between the two groups since both fractions were composed of the same species. Apparent net phytoplankton blooms (in terms of productivity and chlorophyll a) were artifacts of increased chain lengths of nanoplankton diatoms such as Skeletonema costatum, and to a lesser extent, Thalassiosira nordenskioldii Cl. and Detonula confervacea (Cl.) Gran, rather than to the dominance of large, solitary cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature Cited

  • Anderson, G. C. 1965. Fractionation of phytoplankton communities off the Washington and Oregon coasts. Limnol. Oceanogr. 10:477–480.

    Google Scholar 

  • Banse, K. 1976. Rates of growth, respiration and photosynthesis of unicellular algae as related to cell size—a review. J. Phycol. 12:135–140.

    Google Scholar 

  • Bruno, S. F., R. D. Staker, and G. M. Sharma. 1980. Dynamics of phytoplankton productivity in the Peconic Bay estuary, Long Island. Estuarine Coastal Mar. Sci. 10:247–263.

    Article  CAS  Google Scholar 

  • Caperon, J., and J. Meyer. 1972. Nitrogen limited growth of marine phytoplankton. II. Uptake kinetics and their role in nutrient limited growth of phytoplankton. Deep-Sea Res. 19:619–632.

    CAS  Google Scholar 

  • Conover, R. J. 1966. Assimilation of organic matter by zooplankton. Limnol. Oceanogr. 14:701–709.

    Google Scholar 

  • Durbin, E. G., R. W. Krawiec, and T. J. Smayda. 1975. Seasonal studies on the relative importance of different size fractions of phytoplankton in Narragansett Bay (USA). Mar. Biol. 32:271–287.

    Article  CAS  Google Scholar 

  • El-Sayed, S. Z., and J. T. Turner. 1977. Productivity of the Antarctic and tropica/subtropical regions: a comparative study, p. 463–503. In M. J. Dunbar (ed.), Polar Oceans. Arctic Inst. N. America, Calgary.

    Google Scholar 

  • Eppley, R. W. 1972. Temperature and phytoplankton growth in the sea. Fish. Bull. U.S. 70:1063–1085.

    Google Scholar 

  • Eppley, R. W., A. F. Carlucci, O. Holm-Hansen, D. Kiefer, J. J. McCarthy, E. Venrick, and P. M. Williams. 1971. Phytoplankton growth and composition in shipboard cultures supplied with nitrate, ammonia, or urea as the nitrogen source. Limnol. Oceanogr. 16:741–751.

    CAS  Google Scholar 

  • Eppley, R. W., E. H. Renger, E. L. Vanrick, and M. M. Mullin. 1973. A study of phytoplankton dynamics and nutrient cycling in the central gyre of the North Pacific Ocean. Limnol. Oceanogr. 18:534–551.

    CAS  Google Scholar 

  • Eppley, R. W., J. N. Rogers, and J. J. McCarthy. 1969. Half-saturation constants for uptake of nitrate and ammonium by marine phytoplankton. Limnol. Oceanogr. 14:912–920.

    CAS  Google Scholar 

  • Eppley, R. W., and P. R. Sloan. 1966. Growth rates of marine phytoplankton: correlation with light absorption by cell chlorophyll a. Physiol. Plant. 19:47–59.

    Article  CAS  Google Scholar 

  • Frost, B. W. 1972. Effects of size and concentration of food particles on the feeding behavior of the marine planktonic copepod Calanus pacificus. Limnol. Oceanogr. 17:804–815.

    Google Scholar 

  • Gaudy, R. 1974. Feeding four species of pelagic copepods under experimental conditions. Mar. Biol. 25:125–141.

    Article  Google Scholar 

  • Gilmartin, M., and N. Revelante. 1978. The phytoplankton characteristics of the barrier island lagoons of the Gulf of California. Estuarine Coastal Mar. Sci. 7:29–47.

    Article  Google Scholar 

  • Hardy, C. D. 1976. A Preliminary Description of the Peconic Bay Estuary. MSRC Spec. Rept. 3, Mar. Sci. Res. Cent., S.U.N.Y., Stony Brook, 65 p.

    Google Scholar 

  • Hollman, R. 1976. Environment Atlas of Block Island and Long Island Sound Waters. II. Physical and chemical data base at observed and standard depths. 1970–73. New York Ocean Sci. Lab. Tech. Rept. No. 35.

  • Holmes, R. W. 1958. Size fractionation of photosynthesizing phytoplankton. In Physical, Chemical and Biological Oceanographic Observations obtained in Expedition SCOPE in the Eastern Tropical Pacific, Nov.–Dec. 1956. Spec. Scient. Rept. U.S. Fish Wildl. Serv. (Fish.) 279:169–171.

  • Holmes, R. W. 1970. The Secchi disk in turbid coastal waters. Limnol. Oceanogr. 15:688–694.

    Google Scholar 

  • Laws, E. A. 1975. The importance of respiration losses in controlling the size distribution of marine phytoplankton. Ecology 56:419–426.

    Article  Google Scholar 

  • Lorenzen, C. J. 1967. Vertical distribution of chlorophyll and phaeo-pigments: Baja California. Deep-Sea Res. 14:735–745.

    CAS  Google Scholar 

  • Lorenzen, C. J. 1972. Extinction of light in the oce by phytoplankton. J. Cons. Perm. Int. Explor. Mer. 34:262–267.

    Google Scholar 

  • Malone, T. C. 1971a. The relative importance of nanoplankton and netplankton as primary producers in the California Current System. Fish. Bull. U.S. 69:799–820.

    Google Scholar 

  • Malone, T. C. 1971b. Diurnal rhythms in netplankton and nanoplankton assimilation ratios. Mar. Biol. 10:285–289.

    Article  Google Scholar 

  • Malone, T. C. 1971c. The relative importance of nanoplankton and netplankton as primary producers in tropical oceanic and neritic phytoplankton communities. Limnol. Oceanogr. 16:633–639.

    Google Scholar 

  • Malone, T. C. 1976. Phytoplankton productivity in the apex of the New York Bight: environmental regulation of productivity/chlorophyll a, p. 260–272. In M. G. Gross (ed.), The Middle Atlantic Continental Shelf and New York Bight. Limnol. Oceanogr. (Spec. Symp. 2).

  • Malone, T. C. 1977a. Environmental regulation of phytoplankton productivity in the Lower Hudson River estuary. Estuarine Coastal Mar. Sci. 5:157–171.

    Article  CAS  Google Scholar 

  • Malone, T. C. 1977b. Light saturated photosynthesis by phytoplankton size fractions in the New York Bight, USA. Mar. Biol. 42:281–291.

    Article  CAS  Google Scholar 

  • Malone, T. C., and M. B. Chervin. 1979. The production and fate of phytoplankton size fractions in the plume of the Hudson River, N.Y. Bight. Limnol. Oceanogr. 24:683–696.

    CAS  Google Scholar 

  • Martin, J. H. 1970. Phytoplankton-zooplankton relationships in Narragansett Bay. IV. The seasonal importance of grazing. Limnol. Oceanogr. 15:413–418.

    Google Scholar 

  • McCarthy, J. J., W. R. Taylor, and M. E. Loftus. 1974. Significance of nanoplankton in the Chesapeake Bay estuary and problems associated with the measurement of nanoplankton productivity. Mar. Biol. 24:7–16.

    Article  Google Scholar 

  • Morris, I., C. S. Yentsch, and C. M. Yentsch. 1971. The physiological state with respect to nitrogen of phytoplankton from low nutrient subtropical water as measured by the effect of ammonium ion on dark carbon dioxide fixation. Limnol. Oceanogr. 16:859–868.

    Google Scholar 

  • Mullin, M. M. 1963. Some factors affecting the feeding of marine copepods of the genus Calanus. Limnol. Oceanogr. 8:239–250.

    Google Scholar 

  • Munk, W. H., and G. A. Riley. 1952. Adsorption of nutrients by aquatic plants. J. Mar. Res. 11:215–240.

    Google Scholar 

  • Richman, S., and J. N. Rogers. 1969. The feeding of Calanus helgolandicus on synchronously growing populations of the marine diatom Ditylum brightwelli. Limnol. Oceanogr. 14:701–709.

    Google Scholar 

  • Riley, G. A. 1957. Phytoplankton of the north central Sargasso Sea, 1950–1952. Limnol. Oceanogr. 2:252–270.

    Google Scholar 

  • Ryther, J. H., and W. M. Dunstan. 1971. Nitrogen, phosphorus and eutrophication in the coastal marine environment. Science 171:1008–1013.

    Article  CAS  Google Scholar 

  • Saijo, Y., and K. Takasue. 1965. Further studies on the size distribution of photosynthesizing phytoplankton in the Indian Ocean. J. Oceanogr. Soc. Jap. 20:264–271.

    Google Scholar 

  • Smayda, T. J. 1965. A quantitative analysis of the phytoplankton of the Gulf of Panama. II. On the relationship between 14C assimilation and the diatom standing crop. Bull. Inter-Am. Trop. Tuna Comm. 9:467–531.

    Google Scholar 

  • Smayda, T. J. 1973. The growth of Skeletonema costatum during a winter-spring bloom in Narragansett Bay. Norw. J. Bot. 20:219–247.

    Google Scholar 

  • Staker, R. D., and S. F. Bruno. 1978. An annual phytoplankton study in coastal waters off eastern Long Island (Block Island Sound). Bot. Mar. 21:439–449.

    Article  Google Scholar 

  • Strickland, J. D. H., and T. R. Parsons. 1972. A Practical Handbook of Seawater Analysis. Bull. Fish. Res. Board Can. 167:1–311.

    Google Scholar 

  • Syrett, P. J. 1962. Nitrogen assimilation, p. 171–188. In R. A. Lewin (ed.), Biochemistry of Algae. Academic Press, New York.

    Google Scholar 

  • Taguchi, S. 1976. Relationship between photosynthesis and cell size of marine diatoms. J. Phycol. 12:185–189.

    Google Scholar 

  • Turner, J. T. 1982. The annual cycle of zooplankton in a Long Island estuary. Estuaries 5:261–274.

    Article  Google Scholar 

  • Turner, J. T., S. F. Bruno, R. J. Larson, R. D. Staker, and G. M. Sharma. 1983. Seasonality of plankton assemblages in a temperature estuary. Mar. Ecol. (Pubbl. Stn. Zool. Napoli I) 4:81–99.

    Google Scholar 

  • Walsh, J. J., T. E. Whitledge, F. W. Barvenik, C. W. Wirick, and S. O. Howe. 1978. Wind events and food chain dynamics within the New York Bight. Limnol. Oceanogr. 23:659–683.

    Article  CAS  Google Scholar 

  • Williams, R. B. 1964. Division rates of salt marsh diatoms in relation to salinity and cell size. Ecology 45:877–880.

    Article  Google Scholar 

  • Yenstch, C. S., and J. H. Ryther. 1959. Relative significance of the net phytoplankton and nanoplankton in the waters of Vineyard Sound. J. Cons. Perm. Int. Explor. Mer. 24:231–238.

    Google Scholar 

  • Yentsch, C. M., C. S. Yentsch, and L. R. Strube. 1977. Variations in ammonium enhancement, an indication of nitrogen deficiency in New England coastal phytoplankton populations. J. Mar. Res. 35:537–555.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bruno, S.F., Staker, R.D., Sharma, G.M. et al. Primary productivity and phytoplankton size fraction dominance in a temperate North Atlantic estuary. Estuaries 6, 200–211 (1983). https://doi.org/10.2307/1351512

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.2307/1351512

Keywords

Navigation