Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-24T20:35:38.960Z Has data issue: false hasContentIssue false

Marine Pelagic Ciliates and Their Productivity During Summer in Plymouth Coastal Waters

Published online by Cambridge University Press:  11 May 2009

E. D. Pilling
Affiliation:
Department of Biological Sciences, Polytechnic South West, Drake Circus, Plymouth, PL 8AA
R. J. G. Leakey
Affiliation:
Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL 3DH
P. H. Burkill
Affiliation:
Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL 3DH

Extract

The ciliate list for Plymouth waters has been extended by 14 species using modern taxonomic techniques. Ciliates were abundant in the plankton where they formed a significant food resource. Their community biomass and production was estimated to average 12 µ C 1 and 9 µ C 1 respectively during the summer. The ciliate community was dominated by a diverse assemblage of aloricate choreotrichs, suggesting a complex trophic role for this protozoan group.

Ciliate protozoans are ubiquitous and often abundant in marine waters where they are frequently considered to play an important ecological role in trophic flux and nutrient cycling within the plankton (Fenchel, 1987). In spite of this, however, their ecological role in British coastal waters is poorly understood. In Plymouth waters, for instance, there has been only one previous study of marine pelagic Protozoa (Lackey & Lackey, 1963), despite the presence of a marine laboratory in the region for over 100 years. As the study by Lackey & Lackey (1963) focused solely upon the taxonomy of local protists, the ecological role of protozoans in Plymouth waters is unknown. To redress this anomaly the present pilot study was undertaken in Plymouth waters with the following objectives: to identify the dominant ciliates from this region using techniques unavailable to Lackey & Lackey (1963), to quantify ciliate abundance and cell sizes, and to estimate their biomass and production.

Triplicate water samples were collected, using a 3-litre water bottle, from surface waters at each of four stations along a 20-km transect between Plymouth Sound (50°21'N 04°09'W) and the Eddystone Rock (50°ll'N 04°16'W) during June, July and August 1988.

Type
Short Communications
Copyright
Copyright © Marine Biological Association of the United Kingdom 1992

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Burkill, P.H., 1982. Ciliates and other microzooplankton components of a nearshore food-web: standing stocks and production processes. Annales de l'lnstitut Océanographique, Paris, 58, supplement, 335350.Google Scholar
Burkill, P.H., Mantoura, R.F.C., Llewellyn, C.A. & Owens, N.J.P. 1987. Microzooplankton grazing and selectivity of phytoplankton in coastal waters. Marine Biology, 93, 581590.CrossRefGoogle Scholar
Fenchel, T., 1968. The ecology of marine microbenthos. III. The reproductive potential of ciliates. Ophelia, 5, 123126.CrossRefGoogle Scholar
Fenchel, T., 1987. Ecology of Protozoa. New York: Springer-Verlag.Google Scholar
Finlay, B.J., 1978. Community production and respiration by ciliated protozoa in the benthos of a small eutrophic loch. Freshwater Biology, 8, 327341.CrossRefGoogle Scholar
Harris, G.P., 1986. Phytoplankton ecology: structure, function and fluctuation. London: Chapman & Hall.CrossRefGoogle Scholar
Hasle, G.R., 1978. The inverted microscope method. In Phytoplankton Manual (ed. A., Sournia), pp. 8896. Paris: United Nations Education Scientific and Cultural Organisation.Google Scholar
Hedin, H., 1974. Tintinnids on the Swedish west coast. Zoon, 2, 123133.Google Scholar
Krainer, K.H. & Foissner, W., 1990. Revision of the genus Askenasia Blochmann, 1895, with proposal to two new species, and a description of Rhabdoaskenasia minima N.G., N.Sp. (Ciliophora, Cyclotrichida). Journal of Protozoology, 37, 414427.CrossRefGoogle Scholar
Lackey, J.B. & Lackey, E.W., 1963. Microscopic algae and protozoa in the waters near Plymouth in August 1962. Journal of the Marine Biological Association of the United Kingdom, 43, 797805.CrossRefGoogle Scholar
Leppanen, J-M. & Bruun, J-E., 1986. The role of pelagic ciliates including the autotrophic Mesodinium rubrum during the spring bloom of 1982 in the open northern Baltic proper. Ophelia, supplement 4,147157.Google Scholar
Lynn, D.H. & Montagnes, D.J.S., 1988. Taxonomic descriptions of some conspicuous species of strobilidiine ciliates (Ciliophora: Choreotrichida) from the Isles of Shoals, Gulf of Maine. Journal of the Marine Biological Association of the United Kingdom, 68, 639658.CrossRefGoogle Scholar
Lynn, D.H. & Montagnes, D.J.S., 1991. Global production of heterotrophic marine planktonic ciliates. In Protozoa and their role in Marine Processes (ed Reid, P.C. et al), pp. 281308. Springer-Verlag: Berlin. [NATO ASI Series G: Ecological Sciences, Volume G25.]Google Scholar
Lynn, D.H., Montagnes, D.J.S., Dale, T., Gilron, G.L. & Strom, S.L., 1991. A reassessment of the genus Strombidinopsis (Ciliophora: Choreotrichida) with descriptions of four new planktonic species and remarks on its taxonomy and phylogeny. Journal of the Marine Biological Association of the United Kingdom, 71, 597612.CrossRefGoogle Scholar
Lynn, D.H., Montagnes, D.J.S., & Small, E.B., 1988. Taxonomic descriptions of some conspicuous species of the family Strombidiidae (Ciliophora: Oligotrichida) from the Isles of Shoals, Gulf of Maine. Journal of the Marine Biological Association of the United Kingdom, 68, 259276.CrossRefGoogle Scholar
Marshall, S.M., 1969. Protozoa, Order Tintinnida. In Fiches d'identification du zooplancton (ed Fraser, J. H. and Hansen, V. K.), sheets 117127. Conseil International pour l'Exploration de la Mer.Google Scholar
Middlebrook, K., Emerson, C.W., Roff, J.C., & Lynn, D.H., 1987. Distribution and abundance of tintinnids in the Quoddy region of the Bay of Fundy. Canadian Journal of Zoology, 65, 594601.CrossRefGoogle Scholar
Montagnes, D.J.S., & Lynn, D.H., 1987. A quantitative protargol stain (QPS) for ciliates: method description and test of its quantitative nature. Marine Microbial Food Webs, 2, 8393.Google Scholar
Montagnes, D.J.S., Lynn, D.H., Stoecker, D.K. & Small, E.B., 1988a. Taxonomic descriptions of one new species and redescription of four species in the family Strombidiidae (Ciliophora, Oligotrichida). Journal of Protozoology, 35, 189197.CrossRefGoogle Scholar
Montagnes, D.J.S., Lynn, D.H., Roff, J.C., & Taylor, W.D., 1988b. The annual cycle of heterotrophic planktonic ciliates in the waters surrounding the Isles of Shoals, Gulf of Maine: an assessment of their trophic role. Marine Biology, 99, 2130.CrossRefGoogle Scholar
Putt, M. & Stoecker, D.K., (1989). An experimentally determined carbon:volume ratio for marine ‘oligotrichous’ ciliates from estuarine and coastal waters. Limnology and Oceanography, 34, 10971103.CrossRefGoogle Scholar
Revelante, N. & Gilmartin, M. 1983. Microzooplankton distribution in the northern Adriatic Sea with emphasis on the relative abundance of ciliated protozoans. Oceanologia Acta, 6, 407415.Google Scholar
Small, E.B. & Lynn, D.H., 1985. Phylum Ciliophora (Doflein, 1901). In An illustrated guide to the Protozoa (ed. Lee, J.J. et al), pp. 393575. Kansas: Allen.Google Scholar
Stoecker, D.K. 1991. Mixotrophy in marine planktonic ciliates: physiological and ecological aspects of plastid-retention by oligotrichs. In Protozoa and their role in marine Processes (ed P.C., Reid et al.), pp. 161180. Berlin: Springer-Verlag. [NATO ASI Series G: Ecological Sciences, Volume G25.]CrossRefGoogle Scholar
Verity, P.G., 1986. Growth rates of natural tintinnid populations in Narragansett Bay. Marine Ecology Progress Series, 9,117126.CrossRefGoogle Scholar
Verity, P.G., 1987. Abundance, community composition, size distribution and production rates of tintinnids in Narragansett Bay, Rhode Island. Estuarine, Coastal and Shelf Science, 24, 671690.Google Scholar