3 faunally-distinct depth zones: 200 to 800 m (upper slope), 800 to 1425 m (middle slope) and 1425 to 1800 m (lower slope). Differences in δ 15 N and δ 13 C between October 1996 and May 1998 were observed only in the crustaceans Aristeus antennatus and Nematocarcinus exilis. There were few differences among depths in δ 15 N or δ 13 C of benthic fishes or crustaceans: the shrimps A. antennatus and Acanthephyra eximia showed higher δ 15 N values at greater depth, and δ 13 C values of the fishes Alepocephalus rostratus (Alepocephalidae) and Coelorhynchus coelorhynchus (Macrouridae) also tended to increase with increasing depth. Differences in plankton and suprabenthos were also observed among zones (at depth, greater δ 15 N values of gelatinous plankton, calanoid copepods and peracarids were recorded, along with smaller δ 13 C values of gelatinous plankton and peracarids). These are attributed to a microbially-mediated increase in δ 15 N and a reduction in δ 13 C of the particulate material remaining after preferential utilization of labile organic matter in the stable and relatively high (13°C) temperature of the Mediterranean water column. Strong positive correlations between δ 15 N and δ 13 C data for plankton, fishes and crustaceans indicated a single primary source material for these communities, which is attributed to marine snow.
The community structure of decapod crustacean assemblages was established and analysed from two experimental trawl samplings. The data were taken in the south-west Balearic Islands (Algerian Basin, western Mediterranean Sea) at depths ranging from ∼200 to 1800 m. The results of multivariate analysis indicate that the community structure remained constant between samplings. The analysis also revealed that there exist differences between bathyal decapod communities at a regional level (<1000 km) when compared with well-studied nearby areas. The differences relate mainly to the relative contribution of different species and feeding guilds, not to the taxonomic composition of the assemblages studied. It is proposed that these differences result from contrasting surface production regimes (coastal vs open sea) and food web organization (relative dependence on mesopelagic or infaunal prey).
Food resource partitioning and trends in feeding strategies were examined in 3882 individual decapod crustaceans collected from 1989 to 1990, using bottom trawls at depths between 380 and 2261 m in the Catalan Sea (western Mediterranean). The vertical distribution of available food resources near the bottom was the most important factor responsible for food resource partitioning among bathyal decapod crustaceans by depth stratum and season. Decapods were assigned to five different trophic groups according to the food resource exploited and feeding strategy employed (macroplankton feeders, macroplankton-epibenthic feeders, epibenthic feeders, epibenthic-endobenthic feeders, and deposit feeders). There was little dietary overlap, indicating that species did partition the available resources. Overall, dietary overlap values among species increased with depth. Although a trend to increase H’ values for diets with depth was observed, this was not significant (P < 0.10), whereas differences in the percentage of empty stomachs and the frequency of foraminiferans and pteropods in the foreguts increased significantly (P < 0.05) with depth. This last result is indicative of a progressive increase in the importance of deposit feeding in decapod crustaceans as depth increases.
The deep-slope decapod fauna of the Catalan Sea was extensively sampled with an OTSB-14 bottom trawl. A total of 67 bottom tows were taken from 1985 to 1989 at bottom depths ranging from 552 to 2261 m. Species in which abundance decreased with depth were Plesionika acanthonotus, Polycheles typhlops, Calocaris macandreae and Geryon longipes. Highest densities of Acanthephyra eximia, Stereomastis sculpta, and Nematocarcinus exilis were attained at the greatest depths studied. Total abundance, biomass and species richness for decapod crustaceans as a whole decreased with depth. Maximum decapod biomass and diversity occurred on the upper-middle slope on soft bottoms in the .Catalan Sea and in all regions for which data were available. In the Catalan Sea, an oligotrophic area, the abundance of decapods as a group seemed to be higher than in northAtlantic eutrophic regions. In these latter areas, other deep-sea benthic invertebrate groups, particularly ophiuroids, predominate.
Sinking of gelatinous zooplankton biomass is an important component of the biological pump removing carbon from the upper ocean. The export efficiency, e.g., how much biomass reaches the ocean interior sequestering carbon, is poorly known because of the absence of reliable sinking speed data. We measured sinking rates of gelatinous particulate organic matter (jelly-POM) from different species of scyphozoans, ctenophores, thaliaceans, and pteropods, both in the field and in the laboratory in vertical columns filled with seawater using high-quality video. Using these data, we determined taxon-specific jelly-POM export efficiencies using equations that integrate biomass decay rate, seawater temperature, and sinking speed. Two depth scenarios in several environments were considered, with jelly-POM sinking from 200 and 600 m in temperate, tropical, and polar regions. Jelly-POM sank on average between 850 and 1500 m d 21 (salps: 800-1200 m d 21 ; ctenophores: 1200-1500 m d 21 ; scyphozoans: 1000-1100 m d 21 ; pyrosomes: 1300 m d 21 ). High latitudes represent a fast-sinking and low-remineralization corridor, regardless of species. In tropical and temperate regions, significant decomposition takes place above 1500 m unless jelly-POM sinks below the permanent thermocline. Sinking jelly-POM sequesters carbon to the deep ocean faster than anticipated, and should be incorporated into biogeochemical and modeling studies to provide more realistic quantification of export via the biological carbon pump worldwide.
Zonation of deep-sea decapod crustacean fauna was established in the Catalan Sea (Western Mediterranean) based on a total of 66 bottom trawls carried out between 552 and 2261 m depth. An OTSB-14 bottom trawl was used as sampling gear. The main boundaries were located at 1200 to 1300 m and around 1900 to 2000 m. The 1200 to 1300 m boundary separates the decapod communities dwelling on the middle and lower slopes. The most important causes of decapod zonation in the Mediterranean are more closely linked to trophic factors, in view of the fact that basic hydrographic parameters (temperature, salinity) remain constant along the entire slope. In the Catalan Sea impoverlshment of the organic matter content in the bottom sediment with depth and resuspension associated with the steeper portions of the slope (i.e. submarine canyons) are probably the most important factors responsible for the changes recorded. These factors may be directly responsible for the near absence of a variety of organisms that are highly abundant components of the endofauna on the middle slope but disappear below 1200 m. The limits of influence of different macroplanktonic groups (euphausiids, mesopelagic fishes) in the diet of benthic decapods also coincided with the observed boundaries between decapod communities.
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