Benthic suspension feeders: their paramount role in littoral marine food webs

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Abstract

In recent years, particular attention has been paid to coupling and energy transfer between benthos and plankton. Because of their abundance, certain benthic suspension feeders have been shown to have a major impact in marine ecosystems. They capture large quantities of particles and might directly regulate primary production and indirectly regulate secondary production in littoral food chains. Suspension feeders develop dense, three-dimensional communities whose structural complexity depends on flow speed. It has been postulated that these communities can self-organize to enhance food capture and thus establish boundary systems capable of successfully exploiting a less structured system, namely, the plankton.

Section snippets

Evidence for the exploitation of plankton in benthic communities

Recently[12], there have been attempts to assess the individual components of food webs within or between systems and thus achieve an overall understanding of marine ecosystems. Attention has focused on coupling between the benthos and the plankton and, in particular, on energy transfer between the pelagic and benthic ecosystems[13].

The level of exploitation of the plankton by suspension feeders can be measured by direct and indirect methods. Direct methods involve estimating capture rates,

Communities of suspension feeders: life in patches

The colonies or individuals in a population act to slow current flow or increase the residence time of water in their vicinity, thereby increasing the residence time of particles. The substratum, on which the populations rest, also slows the flow and raises turbulence, again increasing the residence time of particles. In the case of closely spaced colonies,the operant hydrodynamic model is interactive flow, whereas in the case of more widely spaced colonies, flow is independent, generating

Suspension feeder communities: a successional approach

The structure (measured as complexity and diversity) and biomass of communities of suspension feeders can increase with food availability. This general pattern is linked to flow speed, with higher flow rates resulting in larger colony and individual sizes[27]. The effect of suspension feeder communities on planktonic ones is a sharp drop in the concentration and an increase in the retention time on the bottom of suspended particles of all kinds, depending on the density of suspension feeders

Suspension feeder communities as a boundary system: from the standpoint of succession and energy transfer

The sea shore is a clear example of a boundary between ecological systems (i.e. the terrestrial and marine). Communities of benthic suspension feeders also lie at a boundary between the substratum (`bottom') and the water column (`sea'). From the standpoint of water column structure and dynamics, the hard bottom benthos—that is, the living stratum immediately above the substratum—has usually been regarded as a sink where the remains of the water column production comes to rest. However, in

Suspension feeder communities in deep areas

Environments with strong, variable currents that are able to transport large concentrations of suspended particles can also be found at great depth on the continental shelf and slope. In fact, any topographical structure that breaks the smooth, even profile of the substratum will bring about a change in the direction and intensity of flow[36](Appendix C). Littoral communities of suspension feeders are usually composed of organisms with short larval development times that act to limit dispersal

The self-organization of suspension feeder communities

Benthic suspension feeders form communities that can self-organize into patches by means of asexual reproduction or dispersal of larvae over short distances. However, the self-organizing concept is not only related to aggregated recruitment. After larval settlement, the number of colonies or individuals that survive decreases during their growth. Survival of suspension feeders is closely related to maximizing prey capture, which involves the spatial organization of all the members in each

Acknowledgements

Part of this paper was presented as a lecture at the `Illa del Rei' University Summer School courses in Menorca, Spain. We are particularly grateful to Prof. R. Margalef for his teaching during those courses. We also wish to thank Dr J.L. Pretus of the University of Barcelona, who organized the courses, and our colleagues Prof. W. Arntz, Prof. J. Ros, Prof. F. Boero, Dr M. Ribes and Dr M. Zabala, as well as two anonymous reviewers, for their critical comments. Support for this work was provided

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