329 resultados para CHONDROPHYCUS FURCATUS


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The ALMOFRONT2 dataset contains mesozooplankton data collected in 1997 - 1998 in the Alboran Sea (South Western Mediterranean Sea) between : 37° 00' N, 2° 54' W and 35° 18' N, 0°00' E.

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The ingestion on ciliates and phytoplankton dataset is based on samples taken during October 2008 in Northern Aegean Sea, the area influenced by the Black Sea water outflow. A Lagrangian experiment was established and copepod ingestion was estimated from experiments performed at stations according to the different positions of drifters during the cruise. Copepods for the experiments were obtained with slow non-quantitative tows from the upper 20 m layer of the water column using 200 µm mesh size nets fitted with a large non-filtering cod end. For the grazing experiments we used the following copepod species: Clausocalanus furcatus, and Temoraa stylifera according to the relevant reference (Bamstedt et al. 2000). Copepod clearance rates on ciliates were calculated according to Frost equations (Frost 1972). Ingestion rates were calculated by multiplying clearance rates by the initial standing stocks (Bamstedt et al. 2000). The egg production dataset is based on samples taken during October 2008 in Northern Aegean Sea, the area influenced by the Black Sea water outflow. A Lagrangian experiment was established and copepod egg production was estimated from experiments performed at stations according to the different positions of drifters during the cruise. Egg production rates of the dominant calanoid copepods were determined by incubation of fertilised females (eggs female/day) collected in the 0-20m layer. Copepod egg production was measured for the copepods Clausocalanus furcatus, Temora stylifera. On board experiments for the estimation of copepod egg production were taken place. For the estimation of copepod production (mgC/m**2/day), lengths (copepods and eggs) were converted to body carbon (Hopcroft et al., 1998) and production was estimated from biomass and weight-specific egg production rates, by assuming that those rates are representative for juvenile specific growth rates (Berggreen et al., 1988).

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Ocean Drilling Program (ODP) Leg 114 recovered nannofossil-bearing sediments from seven sites in the high latitudes of the South Atlantic Ocean. Cretaceous sections were recovered from Sites 698 and 700, located on the Northeast Georgia Rise and its lower flanks, respectively. These contain distinctive high-latitude nannofossil floras similar to those from high-latitude areas of the Northern Hemisphere. Most of the biostratigraphic datums used to date the upper Campanian to Maestrichtian interval appear to lie at approximately the same level in both hemispheres. The FAD of Nephrolithus frequens is confirmed to be diachronous with an earlier occurrence in high latitudes. The LAD of Monomarginatus primus n. sp. also appears to be diachronous with a later LAD in the high latitudes of the Southern Hemisphere. Fossiliferous Paleocene to lowermost Miocene sediments were recovered at all seven sites, from the Northeast Georgia Rise in the west to the Meteor Rise in the east. These nannofossil floras, although restricted in diversity and only poorly preserved, are sufficiently distinctive to allow the recognition of 19 zones and three subzones, which are used to date and correlate the cores recovered. Only Site 704 on the Meteor Rise yielded a substantial section of Miocene to Quaternary nannofossil-rich sediments. The nannofossil floras of this section are of very low diversity, with usually fewer than eight species present. Some stratigraphic ranges of important biostratigraphic datum species are observed to be different in the high-latitude sections from those recorded from low-latitude areas. The LAD of Reticulofenestra bisecta, when calibrated by magnetostratigraphy, appears to occur earlier in Hole 699A (within Chron C6CR) than in Hole 703A and possibly Hole 704B and in other published accounts of lower latitude sites in the South Atlantic. The FAD of Nannotetrina fulgens/N. cristata appears to occur later in Hole 702B (Chron C20R) than it does in other published accounts of lower latitude sites in the South Atlantic. Diachroneity is also suspected in the stratigraphic ranges of Chiasmolithus solitus and Chiasmolithus oamaruensis, although poor magnetostratigraphic results through the critical interval prevent confirmation of this. Differences in the relative stratigraphic ranges of lsthmolithus recurvus and Cribrocentrum coenurumlC. reticulatum at Sites 699 and 703 are noted. These possibly suggest warmer surface waters on the eastern side (Site 703) of the middle to late Eocene South Atlantic than those on the western side (Site 699). The diversities of the nannofossil floras and the presence of the warm-water genera Discoaster, Sphenolithus, Helicosphaera, and Amaurolithus reflect the changing surface water temperatures throughout the Cenozoic. Warmer periods are inferred for the late Paleocene to early middle Eocene, late middle Eocene to late Eocene, latest Oligocene to earliest Miocene, and possibly the Pliocene. Colder periods are inferred for the middle Eocene, most of the Oligocene, and the Miocene. Dramatic changes in the nannofossil floras of the Pleistocene of Site 704 are thought to reflect a rapidly changing environment. Monomarginatus primus, a new species from the Upper Cretaceous strata of Hole 700B, is described.

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Two of five holes drilled at two separate sites during Leg 123 of the Ocean Drilling Program intersected thick and relatively complete sections of Upper Cretaceous-Paleogene nannofossiliferous sediments. Although dominated by turbidite deposition in the upper part, Hole 765C contains a thick and relatively complete Albian-Oligocene section, including a particularly thick Aptian interval, with abundant and fairly well-preserved nannofossils. Several unconformities are confidently interpreted in this section that span much of the Santonian, late Campanian, Maestrichtian, late Eocene, and early Oligocene. Hole 766A contains a thick and relatively complete Albian-lower Eocene section having generally abundant and well-preserved nannofossils. Several unconformities also have been identified in this section that span much of the Coniacian, early Campanian, Maestrichtian, and late Eocene through early Pliocene. The chronostratigraphic position and length of all these unconformities may have considerable significance for reconstructing the sedimentary history and for interpreting the paleoceanography of this region. A particularly thick section of upper Paleocene-lower Eocene sediments, including a complete record across the Paleocene/Eocene boundary, also was cored in Hole 766A that contains abundant and diverse nannofossil assemblages. Although assemblages from this section were correlated successfully using a standard low-latitude zonation, difficulties were encountered that reduced biostratigraphic resolution. Several lines of evidence suggest a mid-latitude position for Site 766 during this time, including (1) high assemblage diversity characteristic of mid-latitude zones of upwelling and (2) absence of certain ecologically controlled markers found only in low latitudes.