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1986) and low level of replication resulting in too low a statistical power (Ragnarrson,<br />

1996).<br />

The present study was observational and not intended to determine the mechanisms<br />

responsible for any differences in abundances between patch and non-patch<br />

communities. However, the increased silt/clay fraction and higher meiofaunal<br />

abundances in patches may have been due to increased passive deposition due to the<br />

reduction in velocity of near-bed flow. In the same way, passive larval entrainment<br />

may be responsible for some of the observed differences in this study. This was<br />

observed even though tube-building spionids have been shown to ingest settling<br />

bivalve larvae (Breese and Phibbs, 1972; Daro and Polk, 1973). Once an individual of<br />

a species had colonised a P. elegans patch, the physico-chemical effects of the tubes<br />

possibly concurred to provide an increased food supply in the form of the flourishing<br />

microbial and meiofaunal communities observed in this study. Furthermore, the<br />

resistance to shearing forces provided by the beds may have allowed a dense<br />

community by virtue of individuals not being 'swept' away (Morgan, 1997).<br />

Increased abundances of meiofauna (43%) were observed by Reise (1983b) in P.<br />

elegans patches compared to areas lacking the spionid, whilst a similar increase has<br />

been documented for beds of another spionid, Polydora ciliata, by Noji (1994), who<br />

suggested that the meiofauna were utilising the worms faecal pellets as a food source.<br />

The presence of C. volutator in patches, while almost completely absent outside<br />

patches, probably resulted from active habitat selection of adults to areas of increased<br />

silt/clay fraction and more stabilised sediments. This amphipod attains particularly<br />

high densities in muddy sediments with high numbers of diatoms (Lawrie, 1996). Its<br />

almost exclusive existence within patches suggests some sort of functional group<br />

interaction (sensu Woodin, 1976) for this tube-building, deposit-feeding amphipod.<br />

Similarly, Reise (1978) noticed C. volutator beds harbouring large numbers of P.<br />

elegans in the Wadden Sea.<br />

Sediment differences between P. elegans patches and non-patch areas.<br />

Sediment analyses indicated that although sediment water content was the same for<br />

patch and non-patch areas, the former consistently contained significantly increased<br />

228

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