Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-26T18:47:47.248Z Has data issue: false hasContentIssue false

Epilithic diatoms of the Clyde Estuary

Published online by Cambridge University Press:  05 December 2011

R. O. McLean
Affiliation:
Department of Biology, Paisley College of Technology, High Street, Paisley PA1 2BE, Scotland
T. A. K. Gow
Affiliation:
The Chemical Defence Establishment, Porton Down, Nr. Salisbury, Wiltshire SP4 OJQ, England
J. Webster
Affiliation:
Department of Biology, Paisley College of Technology, High Street, Paisley PA1 2BE, Scotland
A. Arthur
Affiliation:
Department of Biology, Paisley College of Technology, High Street, Paisley PA1 2BE, Scotland
D. J. Curtis
Affiliation:
Department of Biology, Paisley College of Technology, High Street, Paisley PA1 2BE, Scotland
Get access

Synopsis

Epilithic diatom communities of the Clyde Estuary demonstrated no spring or autumn bloom. Species diversity and dominance were stable at the ends of the estuary and fluctuated through the year in midestuary. Species succession differed from regions where one species dominated throughout the year, e.g. Opephora martyi Heribaud at Bowling (high tide), to those where the dominant species was constantly changing e.g. Erskine (low tide). In all 307 species were recorded, twenty-nine very rare, 172 rare, nineteen were abundant, some e.g. Opephora martyi, Navicula mutica var. cohnii (Hilse) Grun. having wide niche breadth (B>60). others being restricted in their distribution e.g. Nitzschia paleacea Kütz. (B=10.4), Navicula pseudocomoides Hendey (B = 14–8). N. mutica var. cohnii and var. mutica Kütz. were difficult to distinguish in terms of valve morphology, as intermediate forms existed. In the estuary, smaller valves occurred towards the freshwater end. Two clones, originating from a 12/μm and a 26 nm valve (length) corresponding to descriptions of var. cohnii and var. mutica respectively, behaved similarly in culture throughout a range of salinity, in terms of size expression, suggesting no taxonomic difference. Diatom community photosynthesis was affected by salinity, reflecting the site of origin.

Type
Research Article
Copyright
Copyright © Royal Society of Edinburgh 1986

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

Arthur, A., McLean, R. O. & Gow, T. A. K. in press. Polymorphism in Navicula mutica (Kütz.). Proceedings of the Eighth Symposium on Living and Fossil Diatoms, Paris 1984.Google Scholar
Gow, T. A. K. 1985. Studies on Benthic Microalgae in a Polluted Estuary. Ph.D. thesis, Paisley College (C.N.A.A.).Google Scholar
Guillard, R. R. L. 1963. Culture of phytoplankton for feeding marine invertebrates. In Culture of Marine Invertebrate Animals, ed. Smith, R. L. & Chanely, M. H., pp. 2961. New York: Plenum Press.Google Scholar
Hendey, N. I. 1974. The permanganate method for cleaning freshly gathered diatoms. Journal of the Quekett Microscopical Club 32, 423426.Google Scholar
Lund, J. W. G. 1945. Observations on soil algae 1. The ecology, size and taxonomy of British soil diatoms part I. New Phytologist 44, 196219.CrossRefGoogle Scholar
Mclntire, C. D. & Overton, W. S. 1971. Distributional patterns in assemblages of attached diatoms from the Yaquina Estuary. Ecology 53, 758777.CrossRefGoogle Scholar
Webster, J. R. 1983. Nutrition in the Epilithic Diatom Melosira nummuloides (Dill.) C.Ag. Ph.D. thesis Paisley College (C.N.A.A.).Google Scholar