Cores were obtained with a multiple corer at a bathyal site (1320 to 1360m depth) in the Porcupine Seabight during April and July 1982. In July (but not April) the sediment surface was overlain by a layer of phytodetritus, material rapidly sedlmented from the euphotik zone following the spring bloom. The phytodetrital fraction of samples (0 to 1 cm layer of subcores; 3.46 cm2 surface area) removed from the July cores harboured dense, low-diversity populations of benthic foraminifers which resembled the phytodetritus-dwelling assemblages already described from the much deeper (4550 m) BIOTRANS site in the northeast Atlantic. Our new observations consolidate the view that phytodetritus is a microhabitat for some deep-sea benthic foraminiferal species. The bathyal populations were dominated by Alabaminella weddellensis (75 '70 of total) and also included Episton~inella exigua and Tinogullmia sp. nov. These 3 species occurred also in the BIOTRANS phytodetrital assemblages. The April san~ples and the total July samples (phytodetritus plus sediment fractions) yielded diverse foraminiferal populations of similar density and species richness. However, there were some important taxonomic dfferences. In particular, the 8 species consistently present in the phytodetritus were significantly more abundant in the July san~ples, while the most common species in the April sanlples (01.dmrnina sp. nov. A ) was entirely absent during July. We argue that the infhtence of phytodetritus, rather than spatial variability (patchiness), was responsible for some of the differences in species abundances. Other species, however, maintain more stable populat~on densities. Our results suggest that deep-sea benthic foraminifers, like those living in shallow water, probably display a variety of life-history strategies and populdtion dynamics.
INTRODUCTIONThe delivery of organic material to the food-limited deep-sea benthic ecosystem is a central topic in biological oceanography (Angel 1984, Fowler & Knauer 1986, Bruland et al. 1989) One potentially important pathway is provided by rapidly sedimented phytoplankton blooms (Takahashi 1986) which accumulate during the spring and early summer on the sea-floor as a layer of 'phytodetritus'. This material was first reported in sediment cores and bottom photographs taken at depths of 1000 to 4500m in the Porcupine Seabight (an area centred around 51°30'N; 13'00' W) and on the adjacent abyssal plain (Billett et al. 1983, Lampitt 1985, Rice et al. 1986). Elsewhere in the northeast Atlantic it has been observed in the Rockall Trough (Barnett et al. 1982), the northern Bay of Biscay (Sibuet 1984, p. (Gardner et al. 1984). Phytodetritus is known to be ingested by deposit-feeding echinoderms (Billett et al. 1988) and other inegabenthic animals (Thiel et al. in press). Evidence from the BIOTRANS site (4550m depth) indicates that it is also degraded rapidly by deep-sea bacterial populations (Lochte & Turley 1988) and colonised and eaten by small benthic foraminifers (Gooday 1988a). The presen...