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Selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston and cultured algae

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Abstract

I investigated selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston from Chesapeake Bay and laboratory-cultured algae of different sizes or chemical content. In 15 of 16 experiments with complex natural suspensions as food, small(<150 μm) and large (>150 μm) larvae selected most strongly for small (2 to 4 μm) food particles, but in the presence of a large (>10 μm)-cell dinoflagellate bloom, large larvae strongly selected much larger (22 to 30 μm) food material (presumably dinoflagellates). When fed simplified mixtures of four cultured algal species (Synechococcus bacillaris, Isochrysis sp., Dunaliella tertiolecta, and Prorocentrum minimum) ranging in size from 1 to 11 μm, small larvae preferred 1 μm algae while large larvae preferred 11 μm algae. In experiments with algal mixtures, and with suspensions of natural particles and added algae, large larvae preferred algal species harvested from exponential-phase cultures over other species from stationary-phase cultures. Larval ingestion rates of the cultured alga Thalassiosira pseudonana were about three times higher for cells with a low carbon:nitrogen ratio (7.2:1) than for high C:N ratio (16.2:1) cells when these cells were offered separately in suspensions of equal concentration. As a result, more algal cells, algal C, and algal N was ingested by larvae fed low C:N cells. However, larvae did not show a significant preference for either type of cell when they were offered in a 1:1 cell mixture. Feeding patterns of C. virginica larvae in natural food suspensions can vary with the composition of these complex suspensions, and ingestion seems dependent not only on the size, but on the growth rate and chemical quality of food particles.

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References

  • Allan JD, Richman S, Heinle DR, Huff R (1977) Grazing in juvenile stages of some estuarine calanoid copepods. Mar Biol 43: 317–331

    Google Scholar 

  • Appelmans N (1994) Sites of particle selection determined from observations of individual feeding larvae of the sand dollar Dendraster excentricus. Limnol Oceanogr 39: 404–411

    Google Scholar 

  • Baldwin BS (1992) The natural diet and feeding behavior of planktotrophic larvae of the eastern oyster Crassostrea virginica (Gmelin). Doctoral dissertation. University of Maryland, College Park

    Google Scholar 

  • Baldwin BS, Newell RIE (1991) Omnivorous feeding by planktotrophic larvae of the eastern oyster Crassostrea virginica. Mar Ecol Prog Ser 78: 285–301

    Google Scholar 

  • Baldwin BS, Newell RIE (1995) Relative importance of different size food particles in the natural diet of oyster larvae (Crassostrea virginica). Mar Ecol Prog Ser 120: 135–145

    Google Scholar 

  • Bautista B, Harris RP (1992) Copepod gut contents, ingestion rates and grazing impact on phytoplankton in relation to size structure of zooplankton and phytoplankton during a spring bloom. Mar Ecol Prog Ser 82: 41–50

    Google Scholar 

  • Bayne BL (1983) The physiological ecology of marine molluscan larvae. In: Verdonk NH, van den Biggelaar JAM, Tompa A (eds) The Mollusca. Vol III. Development. Academic Press, New York, pp 229–343

    Google Scholar 

  • Berggreen U, Hansen B, Kiørboe T (1988) Food size spectra, ingestion and growth of the copepod Acartia tonsa during development: implications for determination of copepod production. Mar Biol 99: 341–352

    Google Scholar 

  • Bernard C, Rassoulzadegan F (1993) The role of picoplankton (cyanobacteria and plastidic picoflagellates) in the diet of tintinnids. J Plankton Res 15: 361–373

    Google Scholar 

  • Butler NM, Suttle CA, Neill WE (1989) Discrimination by freshwater zooplankton between single algal cells differing in nutritional status. Oecologia 78: 368–372

    Google Scholar 

  • Chesson, J (1978) Measuring preference in selective predation. Ecology 59: 211–215

    Google Scholar 

  • Claustre H, Marty J-C, Cassiani L, Daguat J (1988) Fatty acid dynamics in phytoplankton and microzooplankton communities during a spring bloom in the coastal Ligurian Sea: ecological implications. Mar microb Fd Webs 3: 51–66

    Google Scholar 

  • Confer JL, Moore MV (1987) Interpreting selectivity indices calculated from field data or conditions of prey replacement. Can J Fish aquat Sciences 44: 1529–1533

    Google Scholar 

  • Cowles TJ, Olson RJ, Chisholm SW (1988) Food selection by copepods: discrimination on the basis of food quality. Mar Biol 100: 41–49

    Google Scholar 

  • Davidson K, Flynn KJ, Cunningham A (1991) Relationships between photopigments, cell carbon, cell nitrogen and growth rate for a marine nanoflagellate. J exp mar Biol Ecol 153: 87–96

    Google Scholar 

  • Enright CT, Newkirk GF, Cragie JS, Castell JD (1986) Growth of juvenile Ostrea edulis L. fed Chaetoceros gracilis Schütt of varied chemical composition. J exp mar Biol Ecol 96: 15–26

    Google Scholar 

  • Flaak AR, Epifanio CE (1978) Dietary protein levels and growth of the oyster Crassostrea virginica. Mar Biol 45: 157–163

    Google Scholar 

  • Fritz LW, Lutz RA, Foote MA, Van Dover CL, Ewart JW (1984) Selective feeding and grazing rates of oyster (Crassostrea virginica) larvae on natural phytoplankton assemblages. Estuaries 7: 513–518

    Google Scholar 

  • Gallager SM (1988) Visual observations of particle manipulation during feeding in larvae of a bivalve mollusc. Bull mar Sci 43: 344–365

    Google Scholar 

  • Gallegos CL (1992) Phytoplankton photosynthesis, productivity, and species composition in a eutrophic estuary: comparison of bloom and non-bloom assemblages. Mar Ecol Prog Ser 81: 257–267

    Google Scholar 

  • Gifford DJ (1991) The protozoan-metazoan trophic link in pelagic ecosystems. J Protozool 38: 81–86

    Google Scholar 

  • Goldman JC, McCarthy JJ, Peavey DW (1979) Growth rate influence on the chemical composition of phytoplankton in oceanic waters. Nature, Lond 279: 210–215

    Google Scholar 

  • Guillard RR (1958) Some factors in the use of nanoplankton cultures as food for larval and juvenile bivalves. Proc natn Shellfish Ass 48: 134–142

    Google Scholar 

  • Guillard RR (1975) Culture of phytoplankton for feeding marine invertebrates. In: Smith WL, Chanley MH (eds) Culture of marine invertebrate animals. Plenum Press, New York, pp 29–60

    Google Scholar 

  • Guillard RR, Wangersky PJ (1958) The production of extracellular carbohydrates by some marine flagellates. Limnol Oceanogr 3: 449–454

    Google Scholar 

  • Hansen B (1991) Feeding behaviour in larvae of the opisthobranch Philine apertau. II. Food size spectra and particle selectivity in relation to larval behavior and morphology of the velar structures. Mar Biol 111: 263–270

    Google Scholar 

  • Harrison PJ, Thompson PA, Calderwood GS (1990) Effects of nutrient and light limitation on the biochemical composition of phytoplankton. J appl Phycol 2: 45–56

    Google Scholar 

  • Hart MW (1991) Particle captures and method of suspension feeding by echinoderm larvae. Biol Bull mar biol Lab, Woods Hole 180: 12–27

    Google Scholar 

  • Hitchcock GL (1982) A comparative study of the size-dependent organic composition of marine diatoms and dinoflagellates. J Plankton Res 4: 363–377

    Google Scholar 

  • Houde SEL, Roman MR (1987) Effects of food quality on the functional ingestion response of the copepod Acartia tonsa. Mar Ecol Prog Ser 40: 69–77

    Google Scholar 

  • Huntley ME, Ciminiello P, Lopez MDG (1987) Importance of food quality in determining development and survival of Calanus pacificus (Copepoda: Calanoida). Mar Biol 95: 103–113

    Google Scholar 

  • Huntley ME, Sykes P, Rohan S, Marin V (1986) Chemically-mediated rejection of dinoflagellate prey by the copepods Calanus pacificus and Paracalanus parvus: mechanism, occurrence and significance. Mar Ecol Prog Ser 28: 105–120

    Google Scholar 

  • Ivlev VS (1961) Experimental ecology of the feeding of fishes. Yale University Press, New Haven, Connecticut

    Google Scholar 

  • Jezequel VM, Poulet SA, Harris RP, Moal J, Samain JF (1988) Interspecific and intraspecific composition and variation of free amino acids in marine phytoplankton. Mar Ecol Prog Ser 44: 303–313

    Google Scholar 

  • Kiørboe T, Andersen KP, Dam HG (1990) Coagulation efficiency and aggregate formation in marine phytoplankton. Mar Biol 107: 235–245

    Google Scholar 

  • Kleppel GS, Holliday DV, Pieper RE (1991) Trophic interations between copepods and microplankton: a question about the role of diatoms. Limnol Oceanogr 36: 172–178

    Google Scholar 

  • Langdon CJ, Waldcock MJ (1981) The effect of algal and artificial diets on the growth and fatty acid composition of Crassostrea gigas spat. J mar biol Ass UK 61: 431–448

    Google Scholar 

  • Lechowicz MJ (1982) The sampling characteristics of electivity indices. Oecologia 52: 22–30

    Google Scholar 

  • Lorenzen CJ (1966) A method for the continuous measurement of in vivo chlorophyll concentration. Deep-Sea Res 13: 223–227

    Google Scholar 

  • Luckenbach MW, Sellner KG, Shumway SE, Greene K (1993) Effects of two bloom-forming dinoflagellates, Prorocentrum mariae-labouriae and Gyrodinium uncatenum, on growth and survival of the eastern oyster, Crassostrea virginica (Gmelin, 1791). J Shellfish Res 12: 411–416

    Google Scholar 

  • Mackie G (1969) Quantitative studies of feeding in the oyster Crassostrea virginica. Proc natn Shellfish Ass 59: 6–7 (Abstract)

    Google Scholar 

  • Malej A, Harris RP (1993) Inhibition of copepod grazing by diatom exudates: a factor in the development of mucus aggregates? Mar Ecol Prog Ser 96: 33–42

    Google Scholar 

  • Marin V, Huntley ME, Frost B (1986) Measuring feeding rates of pelagic herbivores: analysis of experimental design and methods. Mar Biol 93: 49–58

    Google Scholar 

  • Moal J, Martin-Jezequel V, Harris RP, Samain J-F, Poulet SA (1987) Interspecific and intraspecific variability of the chemical composition of marine phytoplankton. Oceanol Acta 10: 339–346

    Google Scholar 

  • Morey-Gaines G (1979) The ecological role of red tides in the Los Angeles-Long Beach Harbor food web. In: Taylor DL, Seliger HH (eds) Toxic dinoflagellate blooms. Elsevier North Holland, Inc., New York, pp 315–320

    Google Scholar 

  • Morris I (1981) Photosynthetic products, physiological state, and phytoplankton growth. Can Bull Fish aquat Sciences 210: 83–102

    Google Scholar 

  • Post AF, Dubinsky Z, Wyman K, Falkowski PG (1985) Physiological responses of a marine planktonic diatom to transitions in growth irradiance. Mar Ecol Prog Ser 25: 141–149

    Google Scholar 

  • Poulet SA, Marsot P (1978) Chemosensory grazing by marine calanoid copepods (Arthropoda: Crustacea). Science, NY 200: 1403–1405

    Google Scholar 

  • Rassoulzadegan F, Fenaux L (1979) Grazing of echinoderm larvae (Paracentrotus lividus and Arbacia lixula) on natually occurring particulate matter. J Plankton Res 1: 215–223

    Google Scholar 

  • Rassoulzadegan F, Fenaux L, Strathmann RR (1984) Effect of flavor and size on selection of food by suspension-feeding plutei. Limnol Oceanogr 29: 357–361

    Google Scholar 

  • Richman S, Heinle DR, Huff R (1977) Grazing by adult estuarine calanoid copepods of the Chesapeake Bay. Mar Biol 42: 69–84

    Google Scholar 

  • Riisgård HU (1988) Feeding rates in hard clam (Mercenaria mercenaria) veliger larvae as a function of algal (Isochrysis galbana) concentration. J Shellfish Res 7: 377–380

    Google Scholar 

  • Riisgård HU, Randlov A, Kristensen PS (1980) Rates of water processing, oxygen consumption and efficiency of particle retention in veligers and young post-metamorphic Mytilus edulis. Ophelia 19: 37–47

    Google Scholar 

  • Rivkin RB, Bosch I, Pearse JS, Lessard EJ (1986) Bacterivory: a novel feeding mode for asteroid larvae. Science, NY 223: 1311–1314

    Google Scholar 

  • Scott JM (1980) Effect of growth rate of the food alga on the growth/ingestion efficiency of a marine herbivore. J mar biol Ass UK 60: 681–702

    Google Scholar 

  • Seliger HH, Boggs JA, Rivkin RB, Biggley WH, Aspden KRH (1982) The transport of oyster larvae in an estuary. Mar Biol 71: 57–72

    Google Scholar 

  • Sellner KG, Kachur ME (1987) Phytoplankton: relationships between phytoplankton, nutrients, oxygen flux and secondary producers. In: Heck KL, Jr. (ed) Ecological studies in the middle reach of Chesapeake Bay. Springer-Verlag, New York, pp 12–37

    Google Scholar 

  • Shumway SE (1990a) A review of the effects of algal blooms on shellfish and aquaculture. J Wld Aquacult Soc 21: 65–104

    Google Scholar 

  • Shumway SE (1990b) Auditing the impact of toxic algal blooms on oysters. Envir Auditor 2: 41–56

    Google Scholar 

  • Sprung M (1984) Physiological energetics of mussel larvae (Mytilus edulis). II. Food uptake. Mar Ecol Prog Ser 17: 295–305

    Google Scholar 

  • Steidinger KA (1979) Collection, enumeration, and identification of free-living marine dinoflagellates. In: Taylor DL, Seliger HH (eds) Toxic dinoflagellate blooms. Elsevier North Holland, Inc, New York, pp 319–331

    Google Scholar 

  • Sterner RW, Hagemeir DD, Smith WL, Smith RF (1993) Phytoplankton nutrient limitation and food quality for Daphnia. Limnol Oceanogr 38: 857–871

    Google Scholar 

  • Sterner RW, Smith RF (1993) Clearance, ingestion and release of N and P by Daphnia obtusa feeding on Scenedesmus acutus of varying quality. Bull mar Sci 53: 228–239

    Google Scholar 

  • Strathmann RR (1987) Larval feeding. In: Giese AC, Pearse JS, Pearse VB (eds) Reproduction of marine invertebrates. Vol. IX. General aspects: seeking unity in diversity. Blackwell Scientific Publications, Palo Alto, California, pp 465–550

    Google Scholar 

  • Thompson PA, Harrison PJ (1992) Effects of monospecific algal diets of varying biochemical composition on the growth and survival of Pacific oyster (Crassostrea gigas) larvae. Mar Biol 113: 645–654

    Google Scholar 

  • Utting SD (1986) A preliminary study on the growth of Crassostrea gigas larvae and spat in relation to dietary protein. Aquaculture, Amsterdam 56: 123–138

    Google Scholar 

  • Walne PR (1965) Observations on the influence of food supply and temperature on the feeding and growth of the larvae of Ostrea edulis. Fishery Invest, Lond 2: 24: 1–45

    Google Scholar 

  • Vanderploeg HA, Scavia D (1979) Calculation and use of selectivity coefficients of feeding: zooplankton grazing. Ecol Modelling 7: 135–149

    Google Scholar 

  • Van Valkenburg SD, Flemer DA (1974) The distribution and productivity of nannoplankton in a temperate estuarine area. Estur cstl mar Sci 2: 311–322

    Google Scholar 

  • White AW (1981) Marine zooplankton can accumulate and retain dinoflagellate toxins and cause fish kills. Limnol Oceanogr 26: 103–109

    Google Scholar 

  • Whyte JNC, Bourne N, Hodgson CA (1989) Influence of algal diets on biochemical composition and energy reserves in Patinopecten yessoensis (Jay) larvae. Aquaculture, Amsterdam 78: 333–347

    Google Scholar 

  • Wikfors GH (1986) Altering growth and gross chemical composition of two microalgal molluscan food species by varying nitrate and phosphate. Aquaculture, Amsterdam 59: 1–14

    Google Scholar 

  • Wilson JH (1979) Observations on the grazing rates and growth of Ostrea edulis L. larvae when fed algal cultures of different ages. J exp mar Biol Ecol 38: 187–199

    Google Scholar 

  • Wilson JH (1980) Particle retention and selection by larvae and spat of Ostrea edulis in algal suspensions. Mar Biol 57: 135–145

    Google Scholar 

  • Zubkoff PC, Munday JC, Rhodes RG, Warinner JE (1979) Mesoscale features of summer (1975–1977) dinoflagellate blooms in the York River, Virginia (Chesapeake Bay estuary). In: Taylor DL, Seliger HH (eds) Toxic dinoflagellate blooms. Elsevier North Holland, Inc, New York, pp 279–286

    Google Scholar 

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Communicated by N.H. Marcus, Tallahassee

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Baldwin, B.S. Selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston and cultured algae. Marine Biology 123, 95–107 (1995). https://doi.org/10.1007/BF00350328

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