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  • 2010-2014  (103)
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  • 11
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    PANGAEA
    In:  Supplement to: Bergmann, Melanie; Langwald, Nina; Ontrup, Jörg; Soltwedel, Thomas; Schewe, Ingo; Klages, Michael; Nattkemper, Tim W (2011): Megafaunal assemblages from two shelf stations west of Svalbard. Marine Biology Research, 7(6), 525-539, https://doi.org/10.1080/17451000.2010.535834
    Publication Date: 2023-12-13
    Description: Megafauna plays an important role in benthic ecosystems and contributes significantly to benthic biomass in the Arctic. The distribution is mostly studied using towed cameras. Here, we compare the megafauna from two sites located at different distances from the Kongsfjord: one station at the entrance to the fjord, another on the outer shelf. Although they are only located 25 km apart and at comparable depth, there were significant differences in their species composition. While the inshore station was characterized by shrimps (2.57 +/- 2.18 ind./m**2) and brittlestars (3.21 +/- 3.21 ind./m**2), the offshore site harboured even higher brittlestar densities (15.23 +/- 9.32 ind./m**2) and high numbers of the sea urchin Strongylocentrotus pallidus (1.23 +/- 1.09 ind./m**2). Phytodetrital concentrations of the upper sediment centimetres were significantly higher inshore compared with offshore. At a smaller scale, there were also differences in the composition of different transect sections. Several taxa were characterized by a patchy distribution along transects. We conclude that these differences were caused primarily by habitat characteristics. The seafloor inshore was characterized by glacial soft sediments, whereas the station offshore harboured large quantities of stones. Although the use of a new web-2.0-based tool, BIIGLE (http://www.BIIGLE.de), allowed us to analyse more images (~90) than could have been achieved by hand, taxon area curves indicated that the number of images analysed was not sufficient to capture the species inventory fully. New automated image analysis tools would enable a rapid analysis of larger quantities of camera footage.
    Keywords: Actiniaria; Actiniaria, standard deviation; Actiniidae; Actinostolidae; Alcyonacea; Alcyonacea, standard deviation; Amblyraja radiata; Amblyraja radiata, standard deviation; Amphicteis gunneri; Amphipoda; Amphipoda, standard deviation; Anarhichas minor; Anarhichas minor, standard deviation; Anobothrus gracilis; Anthozoa; Anthozoa, standard deviation; Area/locality; Aristias tumidus; ARK-XXIII/2; Arrhis phyllonyx; Artacama proboscidea; Artediellus atlanticus; Artemisina apollinis; Artemisina apollinis, standard deviation; Ascidiacea; Ascidiacea, standard deviation; Astarte montagui; Asteroidea; Asteroidea, standard deviation; AWI; Brada granulosa; Brada inhabilis; Branchiomma sp.; Bylgides elegans; Bylgides groenlandicus; Capitella capitata; Caridea; Caridea, standard deviation; Ceriantharia; Ceriantharia, standard deviation; Chaetozone spp.; Chirimia biceps; Chlamys islandica; Chone sp.; Ciliatocardium ciliatum; Cirratulus sp.; Colossendeis proboscidea; Colossendeis proboscidea, standard deviation; Colus sabini; Coryphella salmonacea; Crossaster papposus; Crossaster papposus, standard deviation; Crustacea; Crustacea, standard deviation; Cryptonatica affinis; Ctenodiscus crispatus; Cylichna sp.; Dendrobeania cf. fruticosa; Eteone flava; Eteone foliosa; Eunoe nodosa; Euphrosine sp.; Eupyrgus scaber; Event label; Frigidoalvania janmayeni; Gadus morhua; Gadus morhua, standard deviation; Gastropoda; Gastropoda, standard deviation; Gattyana cirrhosa; Gersemia rubiformis; Gersemia rubiformis, standard deviation; Golfingia margaritacea; Gymnelus sp.; Halecium muricatum; Halecium scutum; Halirages fulvocincta; Haploops sp.; Harmothoe sp.; Henricia perforata; Heteromastus filiformis; Hiatella sp.; Hippoglossoides platessoides; Hippoglossoides platessoides, standard deviation; Hormathia digitata; Hormathia nodosa; Hyas spp.; Hyas spp., standard deviation; Icasterias panopla; Icasterias panopla, standard deviation; International Polar Year (2007-2008); IPY; Jasmineira cf. schaudinni; Laonice cf. cirrata; Laonice sp.; Leitoscoloplos mammosus; Lepeta caeca; Leptochiton sp.; Lumbrinereidae; Lumpenus lampretaeformis; Lumpenus lampretaeformis, standard deviation; Lycodes gracilis; Lysippe labiata; Maldane cf. arctica; Maldane sarsi; Maldanidae; Method comment; MF; Microcionidae; Multi frame; Munnopsis typica; Myriapora coarctata; Myriapora coarctata, standard deviation; Myriochele cf. oculata; Myriochele heeri; Myxilla sp.; Nemertea; Neoamphitrite affinis; Nephasoma diaphanes; Nephtys ciliata; Neptunea despecta; Nicomache lumbricalis; Nothria conchylega; Nuculana pernula; Nymphon hirtipes; Oedicerotidae; Oenopota sp.; OFOS photographic survey with BIIGLE analysis; Ophiacantha bidentata; Ophiopholis aculeata; Ophiura robusta; Ophiura sarsi; Ophiuroidea; Ophiuroidea, standard deviation; Pandalus sp.; Paramphithoe hystrix; Pedicellaster typicus; Phascolion strombi; Pherusa sp.; Philine finmarchica; Pholoe cf. assimilis; Phoxocephalus holbolli; Pisces; Pisces, standard deviation; Polarstern; Polynoidae; Porifera; Porifera, standard deviation; Praxillura longissima; Prionospio sp.; PS72; PS72/106-4; PS72/107-4; Pteraster cf. pulvillus; Sabellidae; Sclerocrangon sp.; Scoletoma fragilis; Sepiolidae; Serpulidae; Serpulidae, standard deviation; Similipecten greenlandicus; Solariella obscura; Spiochaetopterus typicus; Spiophanes kroeyeri; Stegocephalopsis ampulla; Stegopoma plicatile; Strongylocentrotus pallidus; Strongylocentrotus pallidus, standard deviation; Syllis cornuta; Tachyrhynchus reticulatus; Tedania suctoria; Terebellides sp.; Themisto sp.; Volutopsius norwegicus; Yoldiella propinqua; Yoldiella solidula; Zoarcidae; Zoarcidae, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 392 data points
    Location Call Number Limitation Availability
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  • 12
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    PANGAEA
    In:  Supplement to: Bergmann, Melanie; Soltwedel, Thomas; Klages, Michael (2011): The interannual variability of megafaunal assemblages in the Arctic deep sea: Preliminary results from the HAUSGARTEN observatory (79°N). Deep Sea Research Part I: Oceanographic Research Papers, 58(6), 711-723, https://doi.org/10.1016/j.dsr.2011.03.007
    Publication Date: 2023-12-13
    Description: Although megafaunal organisms play an important role in deep benthic ecosystems and contribute significantly to benthic biomass in the Arctic little is known about their temporal dynamics. Here, we assessed the interannual dynamics of megafaunal organisms from the HAUSGARTEN observatory in the Fram Strait, an area where the effects of climatic forcing are particularly evident. We analysed three congruent camera transects taken in 2002, 2004 and 2007. Environmental parameters were measured in order to be able to put our faunal results into an environmental context. Our results indicate that although the densities of megafaunal species show different patterns over time, most exhibit an overall decrease between 2002 and 2007 and total megafaunal densities decreased regularly from 2002 to 2004 to 2007 (12.16 +/- 0.96 to 7.41 +/- 0.43 ind/m**2). This concurs with a steady increase in bottom-water temperatures and a decrease in the total organic content and microbial biomass of surficial sediments at the same time period. Although suspension feeder densities also decreased, predator/scavenger and deposit feeder densities have declined to such an extent that suspension feeders accounted for almost 100% of the megafauna in 2007. It could thus be argued that the trophic diversity at the central HAUSGARTEN station (2500 m) has decreased. Temperature-related changes in the production of the surface layers may lead to changes in the quality and/or quantity of particles exported to the deep seafloor. The densities of deposit feeders (i.e. holothurians) peaked (1.14 +/- 0.13 ind/m**2) in 2004, the year following the longest ice cover. These results indicate the importance of ice-related export of particles to the deep seafloor and highlight the need for time-series transects, especially in an era when productive marginal ice zones tend to disappear with the receding sea ice. Although there is a general consensus that the Arctic is in a transition towards a warmer state, only continued observation will allow us to assess if the interannual changes observed are a result of decadal cycles related to the Arctic and North Atlantic Oscillation or if they are indicators of long-term change.
    Keywords: Actiniaria; Actiniaria, standard deviation; Amphipoda; Amphipoda, standard deviation; ARK-XVIII/1; ARK-XX/1; ARK-XXII/1c; Ascorhynchus abyssi; Ascorhynchus abyssi, standard deviation; Asteroidea; Asteroidea, standard deviation; Bathycrinus carpenterii; Bathycrinus carpenterii, standard deviation; Bathycrinus spp.; Bathycrinus spp., standard deviation; Bathyphellia margaritacea; Bathyphellia margaritacea, standard deviation; Burrows; Bythocaris spp.; Bythocaris spp., standard deviation; Caulophacus arcticus; Caulophacus arcticus, standard deviation; Cladorhiza gelida; Cladorhiza gelida, standard deviation; Comatulida; Comatulida, standard deviation; Crustacea; Crustacea, standard deviation; Crustacea indeterminata; Deposit feeder abundance; DEPTH, sediment/rock; Diversity; Elpidia heckeri; Elpidia heckeri, standard deviation; Evenness of species; Event label; Gastropoda; Gastropoda, standard deviation; Gersemia fruticosa; Gersemia fruticosa, standard deviation; Hymenaster pellucidus; Hymenaster pellucidus, standard deviation; International Polar Year (2007-2008); IPY; Isopoda; Isopoda, standard deviation; Kolga hyalina; Kolga hyalina, standard deviation; Lycodes frigidus; Lycodes frigidus, standard deviation; Megafauna, standard deviation; Megafauna abundance; Mohnia spp.; Mohnia spp., standard deviation; Nemertea; Nemertea, standard deviation; North Greenland Sea; Ocean Floor Observation System; OFOS; OFOS photographic survey with BIIGLE analysis; Polarstern; Porifera; Porifera, standard deviation; Porifera indeterminata; Pourtalesia jeffreysi; Pourtalesia jeffreysi, standard deviation; Predator abundance; PS62; PS62/161-3; PS66; PS66/120-1; PS70; PS70/170-1; Saduria megalura; Saduria megalura, standard deviation; Sampling date; Standard deviation; Stones; Suspension feeder abundance; Verum striolatum; Verum striolatum, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 219 data points
    Location Call Number Limitation Availability
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  • 13
    Publication Date: 2014-10-07
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 14
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    PUBLIC LIBRARY SCIENCE
    In:  EPIC3PLoS ONE, PUBLIC LIBRARY SCIENCE, 8(9), pp. e72779, ISSN: 1932-6203
    Publication Date: 2014-10-07
    Description: Knowledge on spatial scales of the distribution of deep-sea life is still sparse, but highly relevant to the understanding of dispersal, habitat ranges and ecological processes. We examined regional spatial distribution patterns of the benthic bacterial community and covarying environmental parameters such as water depth, biomass and energy availability at the Arctic Long-Term Ecological Research (LTER) site HAUSGARTEN (Eastern Fram Strait). Samples from 13 stations were retrieved from a bathymetric (1,284–3,535 m water depth, 54 km in length) and a latitudinal transect (~ 2,500 m water depth; 123 km in length). 454 massively parallel tag sequencing (MPTS) and automated ribosomal intergenic spacer analysis (ARISA) were combined to describe both abundant and rare types shaping the bacterial community. This spatial sampling scheme allowed detection of up to 99% of the estimated richness on phylum and class levels. At the resolution of operational taxonomic units (97% sequence identity; OTU3%) only 36% of the Chao1 estimated richness was recovered, indicating a high diversity, mostly due to rare types (62% of all OTU3%). Accordingly, a high turnover of the bacterial community was also observed between any two sampling stations (average replacement of 79% of OTU3%), yet no direct correlation with spatial distance was observed within the region. Bacterial community composition and structure differed significantly with increasing water depth along the bathymetric transect. The relative sequence abundance of Verrucomicrobia and Planctomycetes decreased significantly with water depth, and that of Deferribacteres increased. Energy availability, estimated from phytodetrital pigment concentrations in the sediments, partly explained the variation in community structure. Overall, this study indicates a high proportion of unique bacterial types on relatively small spatial scales (tens of kilometers), and supports the sampling design of the LTER site HAUSGARTEN to study bacterial community shifts in this rapidly changing area of the world’s oceans.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 15
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    In:  EPIC3Marine Ecology - An evolutionary perspective, 31(4), pp. 1-18
    Publication Date: 2014-09-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 16
    Publication Date: 2014-09-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 17
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    ELSEVIER SCIENCE BV
    In:  EPIC3Sedimentary Geology, ELSEVIER SCIENCE BV, 263-26, pp. 36-44, ISSN: 0037-0738
    Publication Date: 2014-09-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 18
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    In:  EPIC3EuroSITES 2nd Annual Meeting, Trieste, Italien.04.2010., 21
    Publication Date: 2014-09-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 19
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    In:  EPIC3EuroSITES 2nd Annual Meeting, Trieste, Italien.04.2010., 21
    Publication Date: 2014-10-07
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 20
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    In:  EPIC3EuroSITES 2nd Annual Meeting, Trieste, Italien.04.2010., 21
    Publication Date: 2014-09-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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