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  • 1
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    Southend-on-Sea : Aqua Press
    Keywords: Marine invertebrates Europe, Northern ; Marine fishes Europe, Northern ; Marine invertebrates Europe, Northern ; Pictorial works ; Marine fishes Europe, Northern ; Pictorial works ; Bestimmungsbuch ; Europäisches Nordmeer ; Fische ; Wirbellose
    Type of Medium: Image
    Pages: 608 Seiten , Illustrationen
    Edition: 1st english edition
    ISBN: 0954406028 , 8292496084 , 9780954406028 , 9788292496084
    DDC: 592.17733
    Language: English
    Note: "Foreword by David Bellamy" - Umschlag , "First published in Norway by KOM" - Vortitelseite , Literaturverzeichnis: Seiten 587-588 , Literaturangaben
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  • 2
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    PANGAEA
    In:  Supplement to: Andrade, Hector; Renaud, Paul E; Wlodarska-Kowalczuk, Maria; Pardus, Joanna; Carroll, Michael L; Cochrane, Sabine K J; Dahle, Salve; Palerud, Rune (2017): Benthic fauna in soft sediments from the Barents and Pechora Seas. Metadata and database from Akvaplan-niva AS research expeditions, from 1992-2005. Akvaplan-niva Rapport, APN-6770-001, 14 pp, hdl:10013/epic.51439.d001
    Publication Date: 2023-12-13
    Description: Benthic infaunal abundance data from 138 stations in the Barents Sea and surrounding waters are provided in a public database. All samples were collected with a 0.1 m2 van Veen grab and identification was carried out by professional taxonomists. Most abundance data are presented at the species level.
    Keywords: Abietinaria sp.; Abyssoninoe hibernica; Abyssoninoe sp.; Acanthonotozoma cristatum; Acanthonotozoma inflatum; Acanthonotozoma serratum; Acanthonotozoma sp.; Acanthostepheia behringiensis; Acanthostepheia malmgreni; Aceroides latipes; Aceroides sedovi; Acidostoma obesum; Actiniaria indeterminata; Actinia sp.; Actiniidae indeterminata; Admete couthouyi; Admete sp.; Admete viridula; Aeginina longicornis; Aeta sp.; Aglaophamus malmgreni; Alcyonacea indeterminata; Alcyonidium disciforme; Alcyonidium excavatum; Alcyonidium gelatinosum; Alcyonidium gelatinosum andessoni; Alcyonidium mamillatum; Alcyonidium mytili; Alcyonidium protoseideum; Alcyonidium radicellatum; Alcyonidium sp.; Allia sp.; Alvania jeffreysi; Alvania moerchi; Alvania scrobiculata; Alvania sp.; Alvania viridula; Alvania wyvillethomsoni; Amaeana trilobata; Amage auricula; Amauropsis islandica; Ampelisca eschrichtii; Ampelisca macrocephala; Ampelisca sp.; Ampeliscidae indeterminata; Ampharete acutifrons; Ampharete baltica; Ampharete borealis; Ampharete finmarchica; Ampharete goesi; Ampharete lindstroemi; Ampharete sp.; Ampharete vega; Ampharetidae indeterminata; Amphiblestrum auritum; Amphiblestrum septentrionalis; Amphiblestrum solidum; Amphicteis gunneri; Amphicteis ninonae; Amphicteis sundevalli; Amphictene auricoma; Amphilochidae indeterminata; Amphilochus manudens; Amphilochus sp.; Amphipholis torelli; Amphipoda indeterminata; Amphiporidae indeterminata; Amphitrite cirrata; Amphitrite groenlandica; Amphitritinae indeterminata; Amphiura sp.; Amphiura sundevalli; Ampithoe sp.; Anasca spp.; Anatoma crispata; Anobothrus gracilis; Anonyx laticoxae; Anonyx lilljeborgii; Anonyx nugax; Anonyx sarsi; Anonyx sp.; Anopla indeterminata; Antalis entalis; Antalis sp.; Anthozoa indeterminata; Antinoella badia; Antinoella sp.; Aoridae indeterminata; Aphelochaeta marioni; Aphelochaeta sp.; Apherusa sarsii; Aphroditidae indeterminata; Apistobranchus sp.; Apistobranchus tullbergi; Aplacophora spp.; Apomatus sp.; Apseudidae indeterminata; Arachnidium simplex; Arctic_sta1; Arctic_sta10; Arctic_sta11; Arctic_sta118; Arctic_sta119; Arctic_sta12; Arctic_sta122; Arctic_sta128; Arctic_sta13; Arctic_sta133; Arctic_sta135; Arctic_sta140; Arctic_sta141; Arctic_sta145; Arctic_sta148; Arctic_sta15; Arctic_sta151; Arctic_sta159; Arctic_sta16; Arctic_sta161; Arctic_sta162; Arctic_sta163; Arctic_sta17; Arctic_sta171; Arctic_sta174; Arctic_sta178; Arctic_sta18; Arctic_sta21; Arctic_sta22; Arctic_sta24; Arctic_sta26; Arctic_sta28; Arctic_sta29; Arctic_sta31; Arctic_sta32; Arctic_sta34; Arctic_sta4; Arctic_sta45; Arctic_sta47; Arctic_sta48; Arctic_sta5; Arctic_sta50; Arctic_sta5191; Arctic_sta5192; Arctic_sta5193; Arctic_sta52; Arctic_sta54; Arctic_sta5531; Arctic_sta5532; Arctic_sta5533; Arctic_sta5534; Arctic_sta5535; Arctic_sta5536; Arctic_sta5537; Arctic_sta5538; Arctic_sta56; Arctic_sta57; Arctic_sta58; Arctic_sta6; Arctic_sta617; Arctic_sta618; Arctic_sta619; Arctic_sta620; Arctic_sta621; Arctic_sta622; Arctic_sta623; Arctic_sta624; Arctic_sta625; Arctic_sta626; Arctic_sta627; Arctic_sta628; Arctic_sta629; Arctic_sta630; Arctic_sta65; Arctic_sta7; Arctic_sta8; Arctic_sta811; Arctic_sta812; Arctic_sta813; Arctic_sta814; Arctic_sta815; Arctic_sta816; Arctic_sta817; Arctic_sta818; Arctic_sta819; Arctic_sta820; Arctic_sta821; Arctic_sta822; Arctic_sta823; Arctic_sta824; Arctic_sta9; Arctic_staBS1; Arctic_staBS10; Arctic_staBS11; Arctic_staBS12; Arctic_staBS13; Arctic_staBS14; Arctic_staBS15; Arctic_staBS16; Arctic_staBS17; Arctic_staBS18; Arctic_staBS19; Arctic_staBS2; Arctic_staBS20; Arctic_staBS21; Arctic_staBS22; Arctic_staBS23; Arctic_staBS24; Arctic_staBS25; Arctic_staBS26; Arctic_staBS27; Arctic_staBS28; Arctic_staBS29; Arctic_staBS3; Arctic_staBS30; Arctic_staBS31; Arctic_staBS32; Arctic_staBS33; Arctic_staBS34; Arctic_staBS35; Arctic_staBS36; Arctic_staBS37; Arctic_staBS38; Arctic_staBS39; Arctic_staBS4; Arctic_staBS40; Arctic_staBS41; Arctic_staBS42; Arctic_staBS43; Arctic_staBS44; Arctic_staBS45; Arctic_staBS46; Arctic_staBS47; Arctic_staBS5; Arctic_staBS6; Arctic_staBS7; Arctic_staBS8; Arctic_staBS9; Arctica islandica; Arctinula greenlandica; Arctolembos arcticus; Arctonula arctica; Argissa hamatipes; Ariadnaria borealis; Aricidea catherinae; Aricidea hartmani; Aricidea nolani; Aricidea quadrilobata; Aricidea sp.; Arrhinopsis longicornis; Arrhis phyllonyx; Arrhis phyllonyx arcticus; Artacama proboscidea; Ascidiacea indeterminata; Ascidia sp.; Asellota indeterminata; Astarte borealis; Astarte crebricostata; Astarte crenata; Astarte elliptica; Astarte montagui; Astarte sp.; Astarte sulcata; Astartidae indeterminata; Asterias rubens; Asteroidea indeterminata; Astrorhiza limicola; Asychis biceps; Athecata indeterminata; Atylus carinatus; Atylus smittii; Atylus sp.; Augeneria algida; Autolytus sp.; Axinopsida orbiculata; Axionice flexuosa; Axionice maculata; Axiothella sp.; Balanidae indeterminata; Balanus balanus; Balanus crenatus; Balanus sp.; Barents Sea; Bathyarca frielei; Bathyarca glacialis; Bathyarca pectunculoides; Bathyarca sp.; Bispira crassicornis; Bivalvia; Boltenia echinata; Boreonymphon robustum; Boreotrofon sp.; Boreotrophon truncatus; Bowerbankia arctica; Bowerbankia caudata; Bowerbankia imbricata; Bowerbankia sp.; Brachiopoda indeterminata; Brachydiastylis resima; Brachyura indeterminata; Brada granulosa; Brada inhabilis; Brada rugosa; Brada sp.; Brada villosa; Branchiomma arcticum; Branchiomma bombyx; Branchiomma infarctum; Branchiomma sp.; Brisaster fragilis; Brookesena turrita; Bryozoa indeterminata; Buccinidae indeterminata; Buccinum cyaneum; Buccinum glaciale; Buccinum sp.; Buccinum undatum; Buffonellaria biaperta; Buffonellaria divergens; Bugula elongata; Bugula fastigiata; Bugula harmsworthi; Bugula purpurotincta; Bushiella (Jungaria) quadrangularis; Byblis arcticus; Byblis erythrops; Byblis gaimardi; Byblis longicornis; Byblis minuticornis; Byblis sp.; Bylgides elegans; Bylgides groenlandicus; Bylgides promamme; Bylgides sarsi; Bylgides sp.; Caecognathia elongata; Calanoida indeterminata; Calathura brachiata; Calliopiidae indeterminata; Calliopius laeviusculus; Callopora craticula; Callopora lata; Callopora lineata; Callopora obesa; Callopora smitti; Callopora sp.; Callopora whiteavesi; Campanularia volubilis; Campylaspis costata; Campylaspis glabra; Campylaspis horrida; Campylaspis rubicunda; Campylaspis sp.; Campylaspis stephenseni; Campylaspis sulcata; Campylaspis umbensis; Capitella capitata; Capitella sp.; Capitellidae indeterminata; Capnella florida; Capnella glomerata; Caprellidae indeterminata; Cardiidae indeterminata; Carinina sp.; Carinoma sp.; Caudofoveata indeterminata; Cauloramphopus spiniferum; Cellepora nodulosa; Cellepora pumicosa; Cellepora sp.; Celleporella hyalina; Celleporina incrassata; Celleporina sp.; Celleporina surcularis; Celleporina ventricosa; Ceradocus torelli; Cerebratulus longifissus; Cerebratulus sp.; Cerianthus lloydii; Cerianthus sp.; Cerithiella metula; Chaetoderma intermedium; Chaetoderma nitidulum; Chaetoderma sp.; Chaetonymphon sp.; Chaetozone setosa; Chaetozone sp.; Chartella membranaceotruncata; Cheilopora sincera; Cheiloporina sincera; Cheiloporina sp.; Cheilostomatida indeterminata; Chirimia biceps; Chironomidae indeterminata; Chitinopoma serrula; Chlamys islandica; Chlamys sp.; Chone analis; Chone duneri; Chone filicaudata; Chone infundibuliformis; Chone murmanica; Chone paucibranchiata; Chone perseyi; Chone sp.; Ciliatocardium ciliatum; Cingula globosus; Cingula sp.; Circeis armoricana; Circeis spirillum; Cirratulidae indeterminata; Cirratulus caudatus; Cirratulus cirratus; Cirratulus sp.; Cirripedia indeterminata; Cirrophorus branchiatus; Cirrophorus furcatus; Cistenides hyperborea; Clavodorum sp.; Clinocardium ciliatum; Clione limacina; Clymenura borealis; Clymenura polaris; Clymenura sp.; Cnemidocarpa rhizopus; Cnidaria indeterminata; Colus sabini; Colus sp.; Copepoda indeterminata; Corophiidae indeterminata; Corophium bonnellii; Corophium
    Type: Dataset
    Format: text/tab-separated-values, 190164 data points
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  • 3
    ISSN: 1751-8369
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geography , Geosciences
    Notes: Kongsfjorden is a glacial fjord in the Arctic (Svalbard) that is influenced by both Atlantic and Arctic water masses and harbours a mixture of boreal and Arctic flora and fauna. Inputs from large tidal glaciers create steep environmental gradients in sedimentation and salinity along the length of this fjord. The glacial inputs cause reduced biomass and diversity in the benthic community in the inner fjord. Zooplankton suffers direct mortality from the glacial outflow and primary production is reduced because of limited light levels in the turbid, mixed inner waters. The magnitude of the glacial effects diminishes towards the outer fjord. Kongsfjorden is an important feeding ground for marine mammals and seabirds. Even though the fjord contains some boreal fauna, the prey consumed by upper trophic levels is mainly Arctic organisms. Marine mammals constitute the largest top-predator biomass, but seabirds have the largest energy intake and also export nutrients and energy out of the marine environment. Kongsfjorden has received a lot of research attention in the recent past. The current interest in the fjord is primarily based on the fact that Kongsfjorden is particularly suitable as a site for exploring the impacts of possible climate changes, with Atlantic water influx and melting of tidal glaciers both being linked to climate variability. The pelagic ecosystem is likely to be most sensitive to the Atlantic versus Arctic influence, whereas the benthic ecosystem is more affected by long-term changes in hydrography as well as changes in glacial runoff and sedimentation. Kongsfjorden will be an important Arctic monitoring site over the coming decades and a review of the current knowledge, and a gap analysis, are therefore warranted. Important knowledge gaps include a lack of quantitative data on production, abundance of key prey species, and the role of advection on the biological communities in the fjord.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2019-09-23
    Description: The North Sea Benthos Project 2000 was initiated as a follow-up to the 1986 ICES North Sea Benthos Survey with the major aim to identify changes in the macrofauna species distribution and community structure in the North Sea and their likely causes. The results showed that the large-scale spatial distribution of macrofauna communities in the North Sea hardly changed between 1986 and 2000, with the main divisions at the 50 m and 100 m depth contours. Water temperature and salinity as well as wave exposure, tidal stress and primary production were influential environmental factors on a large (North Sea-wide) spatial scale. The increase in abundance and regional changes in distribution of various species with a southern distribution in the North Sea in 2000 were largely associated with an increase in sea surface temperature, primary production and, thus, food supply. This can be most likely related to the North Sea hydro-climate change in the late 1980s influenced by the variability in the North Atlantic Oscillation (NAO). Only one cold-temperate species decreased in abundance in 2000 at most of the stations. Indications for newly established populations of offshore non-native species were not found.
    Type: Article , PeerReviewed
    Format: text
    Format: other
    Format: text
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  • 5
  • 6
    Publication Date: 2014-10-07
    Repository Name: EPIC Alfred Wegener Institut
    Type: Inbook , peerRev
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  • 7
    Publication Date: 2017-08-01
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
    Format: application/pdf
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  • 8
    Publication Date: 2019-07-17
    Description: This study examines whether or not biogeographical and/or managerial divisions across the European seas can be validated using soft-bottom macrobenthic community data. The faunal groups used were: all macrobenthos groups, polychaetes, molluscs, crustaceans, echinoderms, sipunculans and the last 5 groups combined. In order to test the discriminating power of these groups, 3 criteria were used: (1) proximity, which refers to the expected closer faunal resemblance of adjacent areas relative to more distant ones; (2) randomness, which in the present context is a measure of the degree to which the inventories of the various sectors, provinces or regions may in each case be considered as a random sample of the inventory of the next largest province or region in a hierarchy of geographic scales; and (3) differentiation, which provides a measure of the uniqueness of the pattern. Results show that only polychaetes fulfill all 3 criteria and that the only marine biogeographic system supported by the analyses is the one proposed by Longhurst (1998). Energy fluxes and other interactions between the planktonic and benthic domains, acting over evolutionary time scales, can be associated with the multivariate pattern derived from the macrobenthos datasets. Third-stage multidimensional scaling ordination reveals that polychaetes produce a unique pattern when all systems are under consideration. Average island distance from the nearest coast, number of islands and the island surface area were the geographic variables best correlated with the community patterns produced by polychaetes. Biogeographic patterns suggest a vicariance model dominating over the founder-dispersal model except for the semi-closed regional seas, where a model substantially modified from the second option could be supported.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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