519 resultados para Echinodermata


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The MARECHIARA-mesozooplankton dataset contains mesozooplankton data collected in the ongoing time-series at Sation MC (40°48.5' N, 14°15' E) in the Gulf of Naples. This dataset spans over the period 1984-2006 and contains data of mesozooplankton abundance and species composition as well as biomass (as dry weight). Mesozooplankton was regularly sampled in 1984-1990 and 1995-2006, only a few samples were collected in 1991-1992 and no samples in 1993-1994. During the first period of the series sampling frequency was fortnightly, and weekly since 1995.

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The NA64-Mesozooplankton dataset contains biogeochemistry and mesozooplankton data collected in a series of 9 cruises in the Northern Adriatic completed from January 1965 to September 1965 monthly, and December 1965. Biogeochemistry sampling was undertaken using 5L Nansen bottles fired at 0m, 5m, 10m, 20m, 30m and/or bottom depths. The dataset includes 709 samples analysed for nitrate, phosphate, temperature, salinity and density. Mesozooplankton sampling was undertaken at the same locations as for biogeochemistry, using two different net (Hensen non-closing and Appstein closing net). The dataset includes 146 samples analysed for mesozooplankton composition (at higher taxonomic level), abundance and volume settlement. After sedimentation and volume measurement, the fish larva and fish eggs were extracted from samples (egss of Engraulis encrasicholus were determined). Chaetognaths were partly isolated. Identification at higher taxonomic level of zooplankters was completed. Taxonomic identification was done at Smithonian Mediterranean Centre in Salambo. After sedimentation and volume measurement, the fish larva and fish eggs were extracted from samples (egss of Engraulis encrasicholus were determined). Chaetognaths were partly isolated. Identification at higher taxonomic level of zooplankters was completed. Taxonomic identification was done at Smithonian Mediterranean Centre in Salambo.

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The O91- Mesozooplankton dataset is based on samples collected in mid October-mid November 1991 at 20 stations in the South Aegean, the SE.Ionian Sea and in NW Levantine. Samples were collected at discrete layers (from the surface till 300m. These data are published. Sampling volume was estimated by multiplying the mouth area with the wire length. The entire sample (for deep layers) or aliquot of Taxon-specific mesozooplankton abundance (1/4) (for the upper layer) was analyzed under the binocular microscope. Copepod and cladoceran species were identified and enumerated; the other zooplankters were identified and enumerated at higher taxonomic level (commonly named as zooplankton groups). Taxonomic identification was done by I.Siokou-Frangou, E.Christou, and N.Fragopoulu, using the relevant taxonomic literature. The entire sample (for deep layers) or aliquot of Mesozooplankton total abundance (1/4) (for the upper layer) was analyzed under the binocular microscope. All zooplankters were enumerated.

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Sparse to moderately abundant foraminiferal assemblages from Oligocene and Lower Miocene sediments in the CRP-2/2A drillhole contain C.27 genera and 42 species of calcareous benthic foraminifera. No planktic or agglutinated taxa were observed. On the basis of their faunal characteristics, four Foraminiferal Units are defined in drillhole succession: Foraminiferal Unit I (26.91-193.95 mbsf), mostly sparse assemblages with Elphidium magellanicum and Cribroelphidium sp.; Foraminiferal Unit II (193.95-342.42 mbsf), mostly moderately abundant assemblages with Cassidulinoides aequilatera and Eponides bradyi; Foraminiferal Unit III (342.42-486.19 mbsf), moderately abundant to sparse assemblages characterised by Cassidulinoides chapmani and Stainforthia sp.; and Foraminiferal Unit IV, Improverished (486.19-624.15, total depth, mbsf), with mostly barren residues, but with large Milioliidae recorded in situ at various horizons in the drill core. Foraminiferal Units I-IV lack taxa allowing correlation to standard zonal schemes. Inspection of faunal records from CIROS-1 and DSDP 270 indicates that, although the faunas show an overall similarity, CRP-2/2A Foraminiferal Units I-IV are not identifiable at these sites. The units are therefore most likely to reflect local environmental changes, and probably will prove useful for local correlation, but their lateral extent is undetermined. All four assemblages apparently represent various glacially-influenced shelf environments, and appear to reflect a long term deepening trend from Units IV to II, from perhaps inner to mid or outer-shelf depths, followed by a return to shallower, inner shelf, conditios for Unit I.

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The Gollum Channels and Whittard Canyon (NE Atlantic) are two areas that receive high input of organic matter and phytodetritus from euphotic layers, but they are typified by different trophic and hydrodynamic conditions. Sediment biogeochemistry was analysed in conjunction with structure and diversity of the nematode community and differences were tested between study areas, water depths (700 m vs 1000 m), stations, and sediment layers. The Gollum Channels and Whittard Canyon harboured high meiofauna abundances (1054-1426 ind. 10 cm**-2) and high nematode diversity (total of 181 genera). Next to enhanced meiofauna abundance and nematode biomass, there were signs of high levels of organic matter deposition leading to reduced sedimentary conditions, which in turn structured the nematode community. Striking in this respect was the presence of large numbers of 'chemosynthetic' Astomonema nematodes (Astomonema southwardorum, Order Monhysterida, Family Siphonolaimidae). This genus lacks a mouth, buccal cavity and pharynx and possesses a rudimentary gut containing internal, symbiotic prokaryotes which have been recognised as sulphur-oxidising bacteria. Dominance of Astomonema may indicate the presence of reduced environments in the study areas, which is partially confirmed by the local biogeochemical environment. The nematode communities were mostly affected by sediment layer differences and concomitant trophic conditions rather than other spatial gradients related to study area, water depth or station differences, pointing to small-scale heterogeneity as the main source of variation in nematode structure and function. Furthermore, the positive relation between nematode standing stocks, and quantity and quality of the organic matter was stronger when hydrodynamic disturbance was greater. Analogically, this study also suggests that structural diversity can be positively correlated with trophic conditions and that this relation is tighter when hydrodynamic disturbance is greater.