269 resultados para Nemertea


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In der Nordsee wurden auf der Forschungsplattform FINO 1 Felduntersuchungen durchgeführt, um spezielle Fragen zu möglichen Auswirkungen von Offshore-Windenergieparks auf die marine Umwelt zu beantworten. Der Fokus war dabei auf die Konsequenzen für die Lebensgemeinschaft am Meeresboden gerichtet. Es wurden die benthosökologischen Prozesse im Nahbereich der Piles sowie die mittelfristige Entwicklung der Aufwuchsfauna auf der künstlichen Unterwasserstruktur dokumentiert. Die Ansammlung pelagischer Fischen um die Plattform und der Export organischen Materials von der Plattform wurden quantifiziert. Die räumliche Ausdehnung und die Erheblichkeit von Auswirkungen auf die Lebensgemeinschaften des Meeresbodens wurden anhand mathematischer Modellierung abgeschätzt. Zusätzlich wurde die Anwendbarkeit der elektrochemischen Akretionstechnologie zur Schaffung naturnaher Kalksubstrate in der Nordsee getestet und geeignete Parameter für eine erfolgreiche Umsetzung unter Nordseebedingungen ermittelt. Die auch 4,5 Jahre nach Errichtung der Plattform noch ansteigende Artenzahl der Aufwuchsfauna lässt darauf schließen, dass der Sukzessionsprozess noch nicht abgeschlossen ist. Die stark vertikal zonierte Aufwuchsfauna auf der Unterwasserkonstruktion erreicht eine Masse von ca. 5 Tonnen mit ausgeprägten saisonalen Schwankungen. Anhand von echoakustischen Untersuchungen wurden saisonal auftretende Ansammlungen pelagischer Fische um die Plattform dokumentiert. Der Nahbereich der Plattform unterschied sich durch eine Schillauflage und eine räumlich und zeitlich sehr variable Sediment- und Bodenfaunazusammensetzung deutlich von einem Referenzgebiet in 200-400 m Abstand von der Plattform. Eine konzentrische Zonierung mit unterschiedlich stark ausgeprägten Veränderungen der Bodenfauna lässt auf komplexe Veränderung des gesamten lokalen Nahrungsgefüges im Nahbereich der Plattform schließen. Anhand einer Modellierung konnte der Materialexport in die umgebenden Weichbodenbereiche für einzelne Piles und einen hypothetischen Windpark abgeschätzt werden. Die lokale Ausbildung einer hohen Biomasse auf der Unterwasserkonstruktion von WEA sowie der Export mit anschließender Sedimentation lassen zumindest lokal einen erheblichen Einfluss auf Stoff- und Energieflüsse erwarten.

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Structure of assemblages associated with mussel aggregations of Bathymodiolus azoricus was investigated. Mussel beds were found on hydrothermal vent fields on the Mid-Atlantic Ridge (Menez Gwen, Lucky Strike, and Rainbow) at depths 850-2400 m. The community structure of the mussel bed assemblages varied between studied areas. Large number of species was unique to mussel beds of the Menez Gwen field; the most observed taxa were not specialized hydrothermal species. All other nonunique species were found within the Lucky Strike region. The lowest mussel assemblage structure evenness was observed in the shallowest Menez Gwen area (850 m depth). We assume that two types of mussel assemblages (nematode-dominated and copepod-dominated) exist within the Lucky Strike field. The assemblages of B. azoricus differ significantly from assemblages of B. thermophilus inhabiting Pacific hydrothermal vents.

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The Sesame dataset contains mesozooplankton data collected during March 2008 in the Cilician Basin (between between 35.40'- 36.79 N latitude and 33.19- 36.07 E ). Mesozooplankton samples were collected by using a WP-2 closing net with 200 micron mesh size during day hours (07:00-18:00). Samples were taken in the 0-50, 50-100, 100-200 m layer at 6 stations in the Cilician Basin. The dataset includes samples analyzed for mesozooplankton species composition, abundance and total biomass (Dry weight(mg/m**3)). Taxon-specific mesozooplankton abundance: 1/2 sample or an aliquot was analyzed under the binocular microscope. Copepod species were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Taxonomic identification was done at the METU-Institute of Marine Sciences by Tuba Terbiyik using the relevant taxonomic literatures. Mesozooplankton total abundance: 1/2 sample or an aliquot was analyzed under the binocular microscope. Copepod species were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Taxonomic identification was done at the METU-Institute of Marine Sciences using the relevant taxonomic literatures

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Sampling was conducted from March 24 to August 5 2010, in the fjord branch Kapisigdlit located in the inner part of the Godthåbsfjord system, West Greenland. The vessel "Lille Masik" was used during all cruises except on June 17-18 where sampling was done from RV Dana (National Institute for Aquatic Resources, Denmark). A total of 15 cruises (of 1-2 days duration) 7-10 days apart was carried out along a transect composed of 6 stations (St.), spanning the length of the 26 km long fjord branch. St. 1 was located at the mouth of the fjord branch and St. 6 was located at the end of the fjord branch, in the middle of a shallower inner creek . St. 1-4 was covering deeper parts of the fjord, and St. 5 was located on the slope leading up to the shallow inner creek. Mesozooplankton was sampled by vertical net tows using a Hydrobios Multinet (type Mini) equipped with a flow meter and 50 µm mesh nets or a WP-2 net 50 µm mesh size equipped with a non-filtering cod-end. Sampling was conducted at various times of day at the different stations. The nets were hauled with a speed of 0.2-0.3 m s**-1 from 100, 75 and 50 m depth to the surface at St. 2 + 4, 5 and 6, respectively. The content was immediately preserved in buffered formalin (4% final concentration). All samples were analyzed in the Plankton sorting and identification center in Szczecin (www.nmfri.gdynia.pl). Samples containing high numbers of zooplankton were split into subsamples. All copepods and other zooplankton were identified down to lowest possible taxonomic level (approx. 400 per sample), length measured and counted. Copepods were sorted into development stages (nauplii stage 1 - copepodite stage 6) using morphological features and sizes, and up to 10 individuals of each stage was length measured.

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After detachment from benthic habitats, the epibiont assemblages on floating seaweeds undergo substantial changes, but little is known regarding whether succession varies among different seaweed species. Given that floating algae may represent a limiting habitat in many regions, rafting organisms may be unselective and colonize any available seaweed patch at the sea surface. This process may homogenize rafting assemblages on different seaweed species, which our study examined by comparing the assemblages on benthic and floating individuals of the fucoid seaweeds Fucus vesiculosus and Sargassum muticum in the northern Wadden Sea (North Sea). Species richness was about twice as high on S. muticum as on F. vesiculosus, both on benthic and floating individuals. In both seaweed species benthic samples were more diverse than floating samples. However, the species composition differed significantly only between benthic thalli, but not between floating thalli of the two seaweed species. Separate analyses of sessile and mobile epibionts showed that the homogenization of rafting assemblages was mainly caused by mobile species. Among these, grazing isopods from the genus Idotea reached extraordinarily high densities on the floating samples from the northern Wadden Sea, suggesting that the availability of seaweed rafts was indeed limiting. Enhanced break-up of algal rafts associated with intense feeding by abundant herbivores might force rafters to recolonize benthic habitats. These colonization processes may enhance successful dispersal of rafting organisms and thereby contribute to population connectivity between sink populations in the Wadden Sea and source populations from up-current regions.

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In 1986 participants of the Benthos Ecology Working Group of ICES conducted a synoptic mapping of the infauna of the southern and central North Sea. Together with a mapping of the infauna of the northern North Sea by Eleftheriou and Basford (1989, doi:10.1017/S0025315400049158) this provides the database for the description of the benthic infauna of the whole North Sea in this paper. Division of the infauna into assemblages by TWINSPAN analysis separated northern assemblages from southern assemblages along the 70 m depth contour. Assemblages were further separated by the 30, 50 m and 100 m depth contour as well as by the sediment type. In addition to widely distributed species, cold water species do not occur further south than the northern edge of the Dogger Bank, which corresponds to the 50 m depth contour. Warm water species were not found north of the 100 m depth contour. Some species occur on all types of sediment but most are restricted to a special sediment and therefore these species are limited in their distribution. The factors structuring species distributions and assemblages seem to be temperature, the influence of different water masses, e.g. Atlantic water, the type of sediment and the food supply to the benthos.

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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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Macrofaunal assemblages with prevalence of Bresiliidae shrimps and Mytilidae mussels are abundant in at hydrothermal vents along the Mid-Atlantic Ridge. Mussels inhabit zones of diffuse seeps of hydrothermal fluids with temperature abnormalities up to several degrees. Shrimps inhabit an extreme biotope in a mixed interface between seawater and hydrothermal fluids at temperature up to 20-30°C. We studied the mussel and shrimp assemblages in three hydrothermal vent fields: Rainbow, Broken Spur, and Snake Pit. Species richness of the mussel assemblages within at least two fields (Broken Spur and Snake Pit) is higher as compared with shrimps from the same hydrothermal vent fields. Fauna inhibiting shrimp swarms lack almost any taxa specific for particular assemblages: almost all the taxa are also present in the mussel beds. Structure of the shrimp assemblage is less homogeneous as compared with that of the mussel assemblage. Population prevalence of one taxon (Copepoda) in the shrimp assemblage is most likely connected with extreme and unstable conditions of the biotope occupied by the shrimps in a hydrothermal field. Taxonomic similarity between the mussel and shrimp assemblages within one hydrothermal vent field is higher as compared with similarity between the mussel (or shrimp) assemblages from different fields.

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Ongoing zooplankton research at the Plymouth Marine Laboratory has established a time series of zooplankton species since 1988 at L4, a coastal station off Plymouth. Samples were collected by vertical net hauls (WP2 net, mesh 200 µm; UNESCO 1968) from the sea floor (approximately 50 m) to the surface and stored in 4% formalin. Much of the zooplankton analysis has been to the level of "major taxonomic groups" only, and a number of different analysts have participated over the years. The level of expertise has generally been consistent, but the user should be aware that levels of taxonomic discrimination may vary during the course of the dataset. The dominant calanoid copepods are generally well discriminated to species throughout. Calanus has not been routinely examined for species determination, the assumption being that the local population is entirely composed of Calanus helgolandicus. In certain years there has been a particular interest in Temora stylifera, Centropages cherchiae and other species reflected in the dataset. The lack of records in other previous years does not necessarily reflect species absence. We view it as essential for all users of L4 plankton data to establish and maintain contact with the nominated current data originators as well as fully consulting the metadata. While not impinging on free data access, this ensures that this large, species-rich but slightly complex species database is being used in the correct way, and any potential issues with the data are clarified. Furthermore, a proper dialogue with these local experts on the time series will enable where appropriate the most recent sampling timepoints to be used. The data can be downloaded from BODC or from doi:10.1594/PANGAEA.778092 as files for each year by searching for "L4 zooplankton". The most comprehensive dataset is the version downloadable directly from this page. The entire set of zooplankton samples is stored at the Plymouth Marine Laboratory in buffered formalin, and may be available for further taxonomic analysis on request.