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  • 1
    Keywords: Amphipoda Antarctica ; Biodiversity Antarctica ; Hochschulschrift ; Antarktis ; Flohkrebse ; Biodiversität ; Antarktis ; Flohkrebse ; Biodiversität ; Biodiversität ; Flohkrebse ; Höhere Krebse ; Krebstiere
    Type of Medium: Book
    Pages: IV, 148 S. , Ill., graph. Darst., Kt.
    Series Statement: Berichte zur Polar- und Meeresforschung 452
    DDC: 595.378
    RVK:
    RVK:
    Language: German , English
    Note: Texte teilw. dt., teilw. engl , Zugl.: Hamburg, Univ., Diss., 2003
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  • 2
    Keywords: Hochschulschrift ; Grönland West ; Fjord ; Benthos ; Krebstiere ; Zoologie ; Meeresökologie ; Grönland West ; Fjord ; Benthos ; Krebstiere ; Zoologie ; Meeresökologie ; Grönland West ; Ranzenkrebse ; Zoobenthos
    Type of Medium: Book
    Pages: VI, 94 S. , graph. Darst., Kt.
    Series Statement: Berichte zur Polarforschung 363
    DDC: 595.3/7177324
    RVK:
    Language: German
    Note: Zsfassung in engl. Sprache , Teilw. zugl.: Hamburg, Univ., Dipl.-Arb., 2000
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  • 3
    Publication Date: 2024-02-07
    Description: During RV MS Merian expedition MSM75, an international, multidisciplinary team explored the Reykjanes Ridge from June to August 2018. The first area of study, Steinahóll (150–350 m depth), was chosen based on previous seismic data indicating hydrothermal activity. The sampling strategy included ship- and AUV-mounted multibeam surveys, Remotely Operated Vehicle (ROV), Epibenthic Sledge (EBS), and van Veen grab (vV) deployments. Upon returning to Steinahóll during the final days of MSM75, hydrothermal vent sites were discovered using the ROV Phoca (Kiel, GEOMAR). Here we describe and name three new, distinct hydrothermal vent site vulnerable marine ecosystems (VMEs); Hafgufa, Stökkull, Lyngbakr. The hydrothermal vent sites consisted of multiple anhydrite chimneys with large quantities of bacterial mats visible. The largest of the three sites (Hafgufa) was mapped, and reconstructed in 3D. In total 23,310 individual biological specimens were sampled comprising 41 higher taxa. Unique fauna located in the hydrothermally venting areas included two putative new species of harpacticoid copepod (Tisbe sp. nov. and Amphiascus sp. nov.), as well as the sponge Lycopodina cupressiformis (Carter, 1874). Capitellidae Grube, 1862 and Dorvilleidae Chamberlin, 1919 families dominated hydrothermally influenced samples for polychaetes. Around the hydrothermally influenced sites we observed a notable lack of megafauna, with only a few species being present. While we observed hydrothermal associations, the overall species composition is very similar to that seen at other shallow water vent sites in the north of Iceland, such as the Mohns Ridge vent fields, particularly with peracarid crustaceans. We therefore conclude the community overall reflects the usual “background” fauna of Iceland rather than consisting of “vent endemic” communities as is observed in deeper vent systems, with a few opportunistic species capable of utilizing this specialist environment.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Format: archive
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  • 4
    Publication Date: 2024-02-07
    Description: The Ægir Ridge System (ARS) is an ancient extinct spreading axis in the Nordic seas extending from the upper slope east of Iceland (∼550 m depth), as part of its Exclusive Economic Zone (EEZ), to a depth of ∼3,800 m in the Norwegian basin. Geomorphologically a rift valley, the ARS has a canyon-like structure that may promote increased diversity and faunal density. The main objective of this study was to characterize benthic habitats and related macro- and megabenthic communities along the ARS, and the influence of water mass variables and depth on them. During the IceAGE3 expedition (Icelandic marine Animals: Genetics and Ecology) on RV Sonne in June 2020, benthic communities of the ARS were surveyed by means of a remotely-operated vehicle (ROV) and epibenthic sledge (EBS). For this purpose, two working areas were selected, including abyssal stations in the northeast and bathyal stations in the southwest of the ARS. Video and still images of the seabed were usedtoqualitatively describebenthic habitats based on the presence of habitat-forming taxa and the physical environment. Patterns of diversity and community composition of the soft-sediment macrofauna, retrieved from the EBS, were analyzed in a semiquantitative manner. These biological data were complemented by producing high-resolution bathymetric maps using the vessel’s multi-beam echosounder system. As suspected, we were able to identify differences in species composition and number of macro- and megafaunal communities associated with a depth gradient. A biological canyon effect became evident in dense aggregates of megafaunal filter feeders and elevated macrofaunal densities. Analysis of videos and still images from the ROV transects also led to the discovery of a number ofVulnerable Marine Ecosystems (VMEs) dominated by sponges and soft corals characteristic of the Arctic region. Directions for future research encompass a more detailed, quantitative study of the megafauna and more coherent sampling over the entire depth range in order to fully capture the diversity of the habitats and biota of the region. The presence of sensitive biogenic habitats, alongside seemingly high biodiversity and naturalness are supportive of ongoing considerations of designating part of the ARS as an “Ecologically and Biologically Significant Area” (EBSA).
    Type: Article , PeerReviewed
    Format: text
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  • 5
  • 6
    Publication Date: 2023-01-13
    Description: The distribution and diversity of amphipod crustaceans of Icelandic waters, in water depths between 18-3700 m, was examined and how it relates to environmental parameters and depth. Data on amphipod occurrence and abundance were collated from the historical literature (Ingolf Expedition, 1895-96), as well as recent expeditions (1998-2018) such as BioIce (Benthic invertebrates of Icelandic waters) and IceAge (Icelandic marine Animals: Genetics and Ecology, www.iceage-project.org) resulting in 355 amphipod species amongst 71,108 individuals from 532 localities. Samples were taken by a number of trawled sampling devices, including different types of dredges and sledges, as well as Remotely Operated Vehicle (ROV). A 1 ° hexagonal grid was constructed in to map the distribution of the amphipod species alongside twelve environmental factors retrieved from the Bio-Oracle 2.1 database. Due to strong autocorrelation of some of these factors, the analysis was limited to a set of eight variables: depth, pH, phytobiomass, velocity, dissolved oxygen, dissolved iron, salinity, and seabed temperature. Based on these faunistic and environmental data, four biogeographical clusters could be identified: a coastal cluster, a species cluster along the borders of the Greenland-Iceland-Faroe Ridge (GIFR), which separates the deep-sea basins north and south of Iceland, a cluster that is limited to the deep sea to the north of the GIFR, and one that is restricted to the deep-sea south of the GIFR. Diversity as measured by Hill numbers differed considerably between these clusters, with the diversity of the shallow cluster (Coastal and GIFR) to be higher compared to the two deep-sea cluster (Deep North and Deep South). Analysing diversity across a depth gradient, diversity showed a hump-shaped curve with diversity peaking at upper slope (500 m) depth. Depth, salinity and temperature of the seabed were identified as the main parameters to shape the distribution of amphipods around Iceland. Perceived diversity and distribution patterns were discussed with regard to the influence of historical (e.g. oceanography, climatic conditions) and contemporary environmental factors.
    Keywords: Amphipoda Atlantic Crustacea; Ecology & Environment; North; Peracarida; Zoology
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 7
    Publication Date: 2023-05-12
    Keywords: 7709-62; 7709-66; 7709-72; 7709-73; 7709-85; Agassiz Trawl; AGT; Amphipoda Atlantic Crustacea; Arctic Ocean; BC; BIOFAR_St113; BIOFAR_St124; BIOFAR_St15; BIOFAR_St158; BIOFAR_St167; BIOFAR_St168; BIOFAR_St169; BIOFAR_St170; BIOFAR_St171; BIOFAR_St172; BIOFAR_St189; BIOFAR_St19; BIOFAR_St261; BIOFAR_St264; BIOFAR_St267; BIOFAR_St27; BIOFAR_St271; BIOFAR_St274; BIOFAR_St28; BIOFAR_St32; BIOFAR_St380; BIOFAR_St382; BIOFAR_St417; BIOFAR_St421; BIOFAR_St458; BIOFAR_St459; BIOFAR_St481; BIOFAR_St489; BIOFAR_St490; BIOFAR_St493; BIOFAR_St494; BIOFAR_St495; BIOFAR_St499; BIOFAR_St500; BIOFAR_St514; BIOFAR_St515; BIOFAR_St516; BIOFAR_St517; BIOFAR_St522; BIOFAR_St524; BIOFAR_St610; BIOFAR_St65; BIOFAR_St68; BIOFAR_St689; BIOFAR_St691; BIOFAR_St698; BIOFAR_St699; BIOFAR_St70; BIOFAR_St705; BIOFAR_St719; BIOFAR_St73; BIOFAR_St730; BIOFAR_St731; BIOFAR_St736; BIOFAR_St739; BIOFAR_St742; BIOFAR_St744; BIOFAR_St75; BIOFAR_St750; BIOFAR_St770; BIOFAR_St82; BIOFAR_St88; BIOFAR_St89; BIOFAR_St9014; BIOFAR_St95; BIOICE_St2004; BIOICE_St2005; BIOICE_St2006; BIOICE_St2009; BIOICE_St2023; BIOICE_St2042; BIOICE_St2044; BIOICE_St2046; BIOICE_St2049; BIOICE_St2051; BIOICE_St2056; BIOICE_St2057; BIOICE_St2058; BIOICE_St2060; BIOICE_St2061; BIOICE_St2062; BIOICE_St2064; BIOICE_St2067; BIOICE_St2070; BIOICE_St2074; BIOICE_St2075; BIOICE_St2077; BIOICE_St2081; BIOICE_St2086; BIOICE_St2087; BIOICE_St2088; BIOICE_St2089; BIOICE_St2090; BIOICE_St2091; BIOICE_St2093; BIOICE_St2094; BIOICE_St2096; BIOICE_St2097; BIOICE_St2099; BIOICE_St2100; BIOICE_St2103; BIOICE_St2107; BIOICE_St2108; BIOICE_St2110; BIOICE_St2111; BIOICE_St2113; BIOICE_St2114; BIOICE_St2116; BIOICE_St2117; BIOICE_St2118; BIOICE_St2119; BIOICE_St2122; BIOICE_St2124; BIOICE_St2126; BIOICE_St2128; BIOICE_St2129; BIOICE_St2131; BIOICE_St2132; BIOICE_St2134; BIOICE_St2135; BIOICE_St2136; BIOICE_St2137; BIOICE_St2140; BIOICE_St2142; BIOICE_St2143; BIOICE_St2145; BIOICE_St2146; BIOICE_St2147; BIOICE_St2149; BIOICE_St2150; BIOICE_St2152; BIOICE_St2154; BIOICE_St2156; BIOICE_St2161; BIOICE_St2164; BIOICE_St2167; BIOICE_St2170; BIOICE_St2172; BIOICE_St2175; BIOICE_St2177; BIOICE_St2178; BIOICE_St2180; BIOICE_St2201; BIOICE_St2207; BIOICE_St2210; BIOICE_St2212; BIOICE_St2213; BIOICE_St2215; BIOICE_St2219; BIOICE_St2221; BIOICE_St2226; BIOICE_St2229; BIOICE_St2233; BIOICE_St2236; BIOICE_St2237; BIOICE_St2255; BIOICE_St2257; BIOICE_St2265; BIOICE_St2268; BIOICE_St2273; BIOICE_St2282; BIOICE_St2285; BIOICE_St2288; BIOICE_St2299; BIOICE_St2303; BIOICE_St2308; BIOICE_St2311; BIOICE_St2314; BIOICE_St2317; BIOICE_St2318; BIOICE_St2319; BIOICE_St2321; BIOICE_St2322; BIOICE_St2323; BIOICE_St2324; BIOICE_St2325; BIOICE_St2327; BIOICE_St2328; BIOICE_St2330; BIOICE_St2332; BIOICE_St2334; BIOICE_St2337; BIOICE_St2340; BIOICE_St2342; BIOICE_St2345; BIOICE_St2346; BIOICE_St2348; BIOICE_St2349; BIOICE_St2352; BIOICE_St2355; BIOICE_St2356; BIOICE_St2357; BIOICE_St2358; BIOICE_St2359; BIOICE_St2360; BIOICE_St2362; BIOICE_St2363; BIOICE_St2364; BIOICE_St2366; BIOICE_St2367; BIOICE_St2368; BIOICE_St2373; BIOICE_St2374; BIOICE_St2376; BIOICE_St2379; BIOICE_St2380; BIOICE_St2381; BIOICE_St2382; BIOICE_St2393; BIOICE_St2398; BIOICE_St2401; BIOICE_St2403; BIOICE_St2404; BIOICE_St2406; BIOICE_St2407; BIOICE_St2409; BIOICE_St2410; BIOICE_St2412; BIOICE_St2414; BIOICE_St2415; BIOICE_St2417; BIOICE_St2418; BIOICE_St2420; BIOICE_St2423; BIOICE_St2424; BIOICE_St2426; BIOICE_St2427; BIOICE_St2429; BIOICE_St2430; BIOICE_St2431; BIOICE_St2434; BIOICE_St2435; BIOICE_St2438; BIOICE_St2440; BIOICE_St2441; BIOICE_St2451; BIOICE_St2454; BIOICE_St2456; BIOICE_St2457; BIOICE_St2459; BIOICE_St2460; BIOICE_St2463; BIOICE_St2466; BIOICE_St2469; BIOICE_St2472; BIOICE_St2474; BIOICE_St2475; BIOICE_St2480; BIOICE_St2490; BIOICE_St2491; BIOICE_St2493; BIOICE_St2497; BIOICE_St2499; BIOICE_St2501; BIOICE_St2502; BIOICE_St2507; BIOICE_St2508; BIOICE_St2509; BIOICE_St2512; BIOICE_St2514; BIOICE_St2516; BIOICE_St2518; BIOICE_St2522; BIOICE_St2524; BIOICE_St2526; BIOICE_St2527; BIOICE_St2531; BIOICE_St2540; BIOICE_St2545; BIOICE_St2554; BIOICE_St2555; BIOICE_St2564; BIOICE_St2566; BIOICE_St2568; BIOICE_St2570; BIOICE_St2573; BIOICE_St2575; BIOICE_St2576; BIOICE_St2578; BIOICE_St2579; BIOICE_St2581; BIOICE_St2583; BIOICE_St2585; BIOICE_St2588; BIOICE_St2589; BIOICE_St2591; BIOICE_St2594; BIOICE_St2595; BIOICE_St2597; BIOICE_St2606; BIOICE_St2610; BIOICE_St2613; BIOICE_St2616; BIOICE_St2619; BIOICE_St2622; BIOICE_St2629; BIOICE_St2637; BIOICE_St2638; BIOICE_St2648; BIOICE_St2652; BIOICE_St2655; BIOICE_St2660; BIOICE_St2669; BIOICE_St2673; BIOICE_St2675; BIOICE_St2678; BIOICE_St2682; BIOICE_St2692; BIOICE_St2697; BIOICE_St2698; BIOICE_St2700; BIOICE_St2701; BIOICE_St2704; BIOICE_St2707; BIOICE_St2712; BIOICE_St2713; BIOICE_St2717; BIOICE_St2719; BIOICE_St2720; BIOICE_St2726; BIOICE_St2736; BIOICE_St2743; BIOICE_St2745; BIOICE_St2749; BIOICE_St2750; BIOICE_St2751; BIOICE_St2756; BIOICE_St2758; BIOICE_St2759; BIOICE_St2776; BIOICE_St2777; BIOICE_St2779; BIOICE_St2783; BIOICE_St2787; BIOICE_St2789; BIOICE_St2790; BIOICE_St2814; BIOICE_St2823; BIOICE_St2824; BIOICE_St2829; BIOICE_St2830; BIOICE_St2844; BIOICE_St2846; BIOICE_St2849; BIOICE_St2856; BIOICE_St2859; BIOICE_St2860; BIOICE_St2863; BIOICE_St2864; BIOICE_St2867; BIOICE_St2868; BIOICE_St2900; BIOICE_St2904; BIOICE_St2907; BIOICE_St2909; BIOICE_St2912; BIOICE_St2920; BIOICE_St2921; BIOICE_St2923; BIOICE_St2926; BIOICE_St2930; BIOICE_St2932; BIOICE_St2934; BIOICE_St2937; BIOICE_St2939; BIOICE_St2940; BIOICE_St2943; BIOICE_St2944; BIOICE_St2951; BIOICE_St2959; BIOICE_St2976; BIOICE_St2979; BIOICE_St2981; BIOICE_St2983; BIOICE_St2986; BIOICE_St2998; BIOICE_St2999; BIOICE_St3004; BIOICE_St3023; BIOICE_St3025; BIOICE_St3028; BIOICE_St3029; BIOICE_St3032; BIOICE_St3033; BIOICE_St3039; BIOICE_St3043; BIOICE_St3046; BIOICE_St3047; BIOICE_St3048; BIOICE_St3050; BIOICE_St3054; BIOICE_St3056; BIOICE_St3061; BIOICE_St3062; BIOICE_St3067; BIOICE_St3069; BIOICE_St3099; BIOICE_St3108; BIOICE_St3115; BIOICE_St3154; BIOICE_St3158; BIOICE_St3170; BIOICE_St3236; BIOICE_St3246; BIOICE_St3247; BIOICE_St3249; BIOICE_St3250; BIOICE_St3275; BIOICE_St3276; BIOICE_St3280; BIOICE_St3501; BIOICE_St3510; BIOICE_St3515; Box corer; Chlorophyll total; Cruise/expedition; Current velocity; Davis Strait; DEPTH, water; Dredge; DRG; EBS; Ecology & Environment; Epibenthic sledge; Event label; extracted from Bio-Oracle 2.1; Gear; Grab; GRAB; Greenland Sea; IceAGE_1006_1; IceAGE_1010_1; IceAGE_1017_1; IceAGE_1019_1; IceAGE_1032_1; IceAGE_1033_1; IceAGE_1054_1; IceAGE_1057_1; IceAGE_1082_1; IceAGE_1086_1; IceAGE_1104_1; IceAGE_1119_1; IceAGE_1123_1; IceAGE_1132_1; IceAGE_1155_1; IceAGE_1159_1; IceAGE_1168_1; IceAGE_1172_1; IceAGE_1181_1; IceAGE_1184_1; IceAGE_1194_1; IceAGE_1219_1; IceAGE_1222_1; IceAGE_963_1; IceAGE_967_1; IceAGE_979_1; IceAGE_983_1; IceAGE-2_866_7; IceAGE-2_867_1; IceAGE-2_868_3; IceAGE-2_869_2; IceAGE-2_870_4; IceAGE-2_872_4; IceAGE-2_876_5; IceAGE-2_878_1; IceAGE-2_879_5; IceAGE-2_880_2; IceAGE-2_880_3; IceAGE-3_106; IceAGE-3_30; IceAGE-3_37; IceAGE-3_39; IceAGE-3_5; IceAGE-3_55; IceAGE-3_73; IceAGE-3_79; IceAGE-3_85; IceAGE-3_97; IceAGE-RR_106; IceAGE-RR_111; IceAGE-RR_124; IceAGE-RR_127; IceAGE-RR_136; IceAGE-RR_137; IceAGE-RR_149; IceAGE-RR_170; IceAGE-RR_171; IceAGE-RR_188; IceAGE-RR_212; IceAGE-RR_213; IceAGE-RR_216; IceAGE-RR_225; IceAGE-RR_228; IceAGE-RR_24; IceAGE-RR_35; IceAGE-RR_4; IceAGE-RR_64; IceAGE-RR_67; IceAGE-RR_7; IceAGE-RR_80; IceAGE-RR_83; IceAGE-RR_9; Iceland; Iceland Sea; Ingolf; INGOLF-101; INGOLF-102; INGOLF-103; INGOLF-104; INGOLF-105; INGOLF-112; INGOLF-113; INGOLF-115; INGOLF-116; INGOLF-117; INGOLF-118; INGOLF-120; INGOLF-124; INGOLF-126; INGOLF-127; INGOLF-128; INGOLF-138; INGOLF-139; INGOLF-140; INGOLF-143; INGOLF-15; INGOLF-4; INGOLF-40; INGOLF-44; INGOLF-58; INGOLF-6; INGOLF-7; INGOLF-78; INGOLF-80; INGOLF-87; INGOLF-90; INGOLF-95; INGOLF-96; INGOLF-98; Ingolf-Expedition; Iron; Latitude of event; Longitude of
    Type: Dataset
    Format: text/tab-separated-values, 7979 data points
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  • 8
    Publication Date: 2023-07-09
    Keywords: 7709-62; 7709-66; 7709-72; 7709-73; 7709-85; Abludomelita gladiosa; Abludomelita obtusata; Acanthonotozoma cristatum; Acanthonotozoma serratum; Acanthostepheia malmgreni; Aceroides latipes; Aeginella spinosa; Aeginina longicornis; Agassiz Trawl; AGT; Ambasia atlantica; Ampelisca aequicornis; Ampelisca amblyops; Ampelisca compacta; Ampelisca eschrichtii; Ampelisca gibba; Ampelisca islandica; Ampelisca macrocephala; Ampelisca odontoplax; Ampelisca sp.; Ampelisca uncinata; Amphilochoides boecki; Amphilochoides serratipes; Amphilochus anoculus; Amphilochus hamatus; Amphilochus manudens; Amphilochus sp.; Amphilochus tenuimanus; Amphipoda Atlantic Crustacea; Amphithopsis longicaudata; Andaniella pectinata; Andaniexis abyssi; Andaniexis lupus; Andaniexis sp.; Andaniopsis nordlandica; Andaniopsis pectinata; Anonyx sp.; Apherusa glacialis; Apherusa sarsii; Apherusa sp.; Arctic Ocean; Argissa hamatipes; Arrhinopsis sp.; Arrhis phyllonyx; Arrhis sp.; Astyra abyssi; Astyra sp.; Austrosyrrhoe septentrionalis; Austrosyrrhoe sp.; Autonoe borealis; Bathymedon longimanus; Bathymedon obtusifrons; Bathymedon saussurei; Bathymedon sp.; BC; BIOFAR_St113; BIOFAR_St124; BIOFAR_St15; BIOFAR_St158; BIOFAR_St167; BIOFAR_St168; BIOFAR_St169; BIOFAR_St170; BIOFAR_St171; BIOFAR_St172; BIOFAR_St189; BIOFAR_St19; BIOFAR_St261; BIOFAR_St264; BIOFAR_St267; BIOFAR_St27; BIOFAR_St271; BIOFAR_St274; BIOFAR_St28; BIOFAR_St32; BIOFAR_St380; BIOFAR_St382; BIOFAR_St417; BIOFAR_St421; BIOFAR_St458; BIOFAR_St459; BIOFAR_St481; BIOFAR_St489; BIOFAR_St490; BIOFAR_St493; BIOFAR_St494; BIOFAR_St495; BIOFAR_St499; BIOFAR_St500; BIOFAR_St514; BIOFAR_St515; BIOFAR_St516; BIOFAR_St517; BIOFAR_St522; BIOFAR_St524; BIOFAR_St610; BIOFAR_St65; BIOFAR_St68; BIOFAR_St689; BIOFAR_St691; BIOFAR_St698; BIOFAR_St699; BIOFAR_St70; BIOFAR_St705; BIOFAR_St719; BIOFAR_St73; BIOFAR_St730; BIOFAR_St731; BIOFAR_St736; BIOFAR_St739; BIOFAR_St742; BIOFAR_St744; BIOFAR_St75; BIOFAR_St750; BIOFAR_St770; BIOFAR_St82; BIOFAR_St88; BIOFAR_St89; BIOFAR_St9014; BIOFAR_St95; BIOICE_St2004; BIOICE_St2005; BIOICE_St2006; BIOICE_St2009; BIOICE_St2023; BIOICE_St2042; BIOICE_St2044; BIOICE_St2046; BIOICE_St2049; BIOICE_St2051; BIOICE_St2056; BIOICE_St2057; BIOICE_St2058; BIOICE_St2060; BIOICE_St2061; BIOICE_St2062; BIOICE_St2064; BIOICE_St2067; BIOICE_St2070; BIOICE_St2074; BIOICE_St2075; BIOICE_St2077; BIOICE_St2081; BIOICE_St2086; BIOICE_St2087; BIOICE_St2088; BIOICE_St2089; BIOICE_St2090; BIOICE_St2091; BIOICE_St2093; BIOICE_St2094; BIOICE_St2096; BIOICE_St2097; BIOICE_St2099; BIOICE_St2100; BIOICE_St2103; BIOICE_St2107; BIOICE_St2108; BIOICE_St2110; BIOICE_St2111; BIOICE_St2113; BIOICE_St2114; BIOICE_St2116; BIOICE_St2117; BIOICE_St2118; BIOICE_St2119; BIOICE_St2122; BIOICE_St2124; BIOICE_St2126; BIOICE_St2128; BIOICE_St2129; BIOICE_St2131; BIOICE_St2132; BIOICE_St2134; BIOICE_St2135; BIOICE_St2136; BIOICE_St2137; BIOICE_St2140; BIOICE_St2142; BIOICE_St2143; BIOICE_St2145; BIOICE_St2146; BIOICE_St2147; BIOICE_St2149; BIOICE_St2150; BIOICE_St2152; BIOICE_St2154; BIOICE_St2156; BIOICE_St2161; BIOICE_St2164; BIOICE_St2167; BIOICE_St2170; BIOICE_St2172; BIOICE_St2175; BIOICE_St2177; BIOICE_St2178; BIOICE_St2180; BIOICE_St2201; BIOICE_St2207; BIOICE_St2210; BIOICE_St2212; BIOICE_St2213; BIOICE_St2215; BIOICE_St2219; BIOICE_St2221; BIOICE_St2226; BIOICE_St2229; BIOICE_St2233; BIOICE_St2236; BIOICE_St2237; BIOICE_St2255; BIOICE_St2257; BIOICE_St2265; BIOICE_St2268; BIOICE_St2273; BIOICE_St2282; BIOICE_St2285; BIOICE_St2288; BIOICE_St2299; BIOICE_St2303; BIOICE_St2308; BIOICE_St2311; BIOICE_St2314; BIOICE_St2317; BIOICE_St2318; BIOICE_St2319; BIOICE_St2321; BIOICE_St2322; BIOICE_St2323; BIOICE_St2324; BIOICE_St2325; BIOICE_St2327; BIOICE_St2328; BIOICE_St2330; BIOICE_St2332; BIOICE_St2334; BIOICE_St2337; BIOICE_St2340; BIOICE_St2342; BIOICE_St2345; BIOICE_St2346; BIOICE_St2348; BIOICE_St2349; BIOICE_St2352; BIOICE_St2355; BIOICE_St2356; BIOICE_St2357; BIOICE_St2358; BIOICE_St2359; BIOICE_St2360; BIOICE_St2362; BIOICE_St2363; BIOICE_St2364; BIOICE_St2366; BIOICE_St2367; BIOICE_St2368; BIOICE_St2373; BIOICE_St2374; BIOICE_St2376; BIOICE_St2379; BIOICE_St2380; BIOICE_St2381; BIOICE_St2382; BIOICE_St2393; BIOICE_St2398; BIOICE_St2401; BIOICE_St2403; BIOICE_St2404; BIOICE_St2406; BIOICE_St2407; BIOICE_St2409; BIOICE_St2410; BIOICE_St2412; BIOICE_St2414; BIOICE_St2415; BIOICE_St2417; BIOICE_St2418; BIOICE_St2420; BIOICE_St2423; BIOICE_St2424; BIOICE_St2426; BIOICE_St2427; BIOICE_St2429; BIOICE_St2430; BIOICE_St2431; BIOICE_St2434; BIOICE_St2435; BIOICE_St2438; BIOICE_St2440; BIOICE_St2441; BIOICE_St2451; BIOICE_St2454; BIOICE_St2456; BIOICE_St2457; BIOICE_St2459; BIOICE_St2460; BIOICE_St2463; BIOICE_St2466; BIOICE_St2469; BIOICE_St2472; BIOICE_St2474; BIOICE_St2475; BIOICE_St2480; BIOICE_St2490; BIOICE_St2491; BIOICE_St2493; BIOICE_St2497; BIOICE_St2499; BIOICE_St2501; BIOICE_St2502; BIOICE_St2507; BIOICE_St2508; BIOICE_St2509; BIOICE_St2512; BIOICE_St2514; BIOICE_St2516; BIOICE_St2518; BIOICE_St2522; BIOICE_St2524; BIOICE_St2526; BIOICE_St2527; BIOICE_St2531; BIOICE_St2540; BIOICE_St2545; BIOICE_St2554; BIOICE_St2555; BIOICE_St2564; BIOICE_St2566; BIOICE_St2568; BIOICE_St2570; BIOICE_St2573; BIOICE_St2575; BIOICE_St2576; BIOICE_St2578; BIOICE_St2579; BIOICE_St2581; BIOICE_St2583; BIOICE_St2585; BIOICE_St2588; BIOICE_St2589; BIOICE_St2591; BIOICE_St2594; BIOICE_St2595; BIOICE_St2597; BIOICE_St2606; BIOICE_St2610; BIOICE_St2613; BIOICE_St2616; BIOICE_St2619; BIOICE_St2622; BIOICE_St2629; BIOICE_St2637; BIOICE_St2638; BIOICE_St2648; BIOICE_St2652; BIOICE_St2655; BIOICE_St2660; BIOICE_St2669; BIOICE_St2673; BIOICE_St2675; BIOICE_St2678; BIOICE_St2682; BIOICE_St2692; BIOICE_St2697; BIOICE_St2698; BIOICE_St2700; BIOICE_St2701; BIOICE_St2704; BIOICE_St2707; BIOICE_St2712; BIOICE_St2713; BIOICE_St2717; BIOICE_St2719; BIOICE_St2720; BIOICE_St2726; BIOICE_St2736; BIOICE_St2743; BIOICE_St2745; BIOICE_St2749; BIOICE_St2750; BIOICE_St2751; BIOICE_St2756; BIOICE_St2758; BIOICE_St2759; BIOICE_St2776; BIOICE_St2777; BIOICE_St2779; BIOICE_St2783; BIOICE_St2787; BIOICE_St2789; BIOICE_St2790; BIOICE_St2814; BIOICE_St2823; BIOICE_St2824; BIOICE_St2829; BIOICE_St2830; BIOICE_St2844; BIOICE_St2846; BIOICE_St2849; BIOICE_St2856; BIOICE_St2859; BIOICE_St2860; BIOICE_St2863; BIOICE_St2864; BIOICE_St2867; BIOICE_St2868; BIOICE_St2900; BIOICE_St2904; BIOICE_St2907; BIOICE_St2909; BIOICE_St2912; BIOICE_St2920; BIOICE_St2921; BIOICE_St2923; BIOICE_St2926; BIOICE_St2930; BIOICE_St2932; BIOICE_St2934; BIOICE_St2937; BIOICE_St2939; BIOICE_St2940; BIOICE_St2943; BIOICE_St2944; BIOICE_St2951; BIOICE_St2959; BIOICE_St2976; BIOICE_St2979; BIOICE_St2981; BIOICE_St2983; BIOICE_St2986; BIOICE_St2998; BIOICE_St2999; BIOICE_St3004; BIOICE_St3023; BIOICE_St3025; BIOICE_St3028; BIOICE_St3029; BIOICE_St3032; BIOICE_St3033; BIOICE_St3039; BIOICE_St3043; BIOICE_St3046; BIOICE_St3047; BIOICE_St3048; BIOICE_St3050; BIOICE_St3054; BIOICE_St3056; BIOICE_St3061; BIOICE_St3062; BIOICE_St3067; BIOICE_St3069; BIOICE_St3099; BIOICE_St3108; BIOICE_St3115; BIOICE_St3154; BIOICE_St3158; BIOICE_St3170; BIOICE_St3236; BIOICE_St3246; BIOICE_St3247; BIOICE_St3249; BIOICE_St3250; BIOICE_St3275; BIOICE_St3276; BIOICE_St3280; BIOICE_St3501; BIOICE_St3510; BIOICE_St3515; Box corer; Bruzelia sp.; Bruzelia tuberculata; Byblis crassicornis; Byblis erythrops; Byblis gaimardii; Byblis medialis; Byblis minuticornis; Byblisoides bellansantiniae; Byblis sp.; Calliopius laeviusculus; Camacho faroensis; Caprella ciliata; Caprella dubia; Caprella microtuberculata; Caprella rinki; Caprella septentrionalis; Chevreuxius grandimanus; Cleippides bicuspis; Cleippides quadricuspis; Cleippides tricuspis; Cleonardopsis sp.; Cleonardo sp.; Corophiidira sp.; Cressa carinata; Cressa jeanjusti; Cressa minuta; Cressa quinquedentata; Cressina monocuspis; Cruise/expedition; Davis Strait; Deflexilodes norvegicus; Deflexilodes rostratus; Deflexilodes subnudus; Deflexilodes tenuirostratus; Deflexilodes tesselatus; Deflexilodes
    Type: Dataset
    Format: text/tab-separated-values, 190455 data points
    Location Call Number Limitation Availability
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  • 9
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Lörz, Anne-Nina; Smith, Peter; Linse, Katrin; Steinke, Dirk (2012): High genetic diversity within Epimeria georgiana (Amphipoda) from the southern Scotia Arc. Marine Biodiversity, 42(2), 137-159, https://doi.org/10.1007/s12526-011-0098-8
    Publication Date: 2023-12-13
    Description: DNA barcoding revealed four well-supported clades among amphipod specimens that keyed out to Epimeria georgiana Schellenberg, 1931, three clades with specimens from the southern Scotia Arc and one clade with specimens from the Weddell Sea. Detailed morphological investigations of sequenced specimens were conducted, through light and scanning electron microscopy. High magnification (500-2,000 fold) revealed features such as comb-scales on the first antenna and trich bearing pits on the fourth coxal plate to be similar for all specimens in the four clades. Consistent microstructure character differences in the Weddell Sea specimens combined with high genetic distances (COI divergence〉20%) allowed the description of Epimeria angelikae, a species new to science. Specimens of E. georgiana in the other three COI clades from the Scotia Arc were morphologically indistinguishable. Representative specimens of clade A are also illustrated in detail. Our results on the high genetic divergences in epimeriid amphipods support the theory of the southern Scotia Arc being a centre of Antarctic diversification.
    Keywords: 044; Agassiz Trawl; AGT; ANT-XIV/2; ANT-XVII/3; ANT-XXI/2; Area/locality; BIOPEARL I JR144 JR145 JR146, JR147, JR149; BioRoss; Bottom trawl; BT; Comment; Cruise/expedition; DATE/TIME; Deception Island; Depth, bottom/max; Depth, top/min; DEPTH, water; EBS; Epibenthic sledge; Event label; Identification; International Polar Year (2007-2008); IPY; IPY-CAML; James Clark Ross; JR144/EI-AGT-2; JR144/EI-AGT-3; JR144/EI-AGT-4; JR144/PB-AGT-2; JR20060226; Latitude of event; Longitude of event; MULT; Multiple investigations; Polarstern; PS42; PS42/044; PS56/177-1; PS56/183-1; PS56 EASIZ III; PS65/232-1; PS65/233-1; PS65 BENDEX; Ross Sea; Sample amount; Scotia Sea; South Georgia Island; South Shetland Islands; Species; Station label; Swenska_Sypolar/34; TAN0402; TAN0402/134; TAN0402/184c; TAN0402/233; TAN0402/33; TAN0402/94; TAN0802; TAN0802/161; TAN0802/17; TAN0802/56; Tangaroa; Weddell Sea
    Type: Dataset
    Format: text/tab-separated-values, 346 data points
    Location Call Number Limitation Availability
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  • 10
    facet.materialart.
    Unknown
    SPRINGER
    In:  EPIC3Marine Biology, SPRINGER, 165, pp. 184, ISSN: 0025-3162
    Publication Date: 2018-11-27
    Description: Small herbivores are abundant on large marine macrophytes, but their impact on their hosts is poorly understood relativeuto large grazers such as urchins and fish. To limit the risks of predation, many marine mesograzers live within nests or burrows,upotentially causing more damage to plants than predicted from consumption alone. To test whether the growth ofularge primary producers can be affected by modification of plant structures by small herbivores, we quantified the effect ofuthe nest-building amphipod Pseudopleonexes lessoniae on blades of the giant kelp, Macrocystis pyrifera in New Zealand.uAmphipods create their nests by rolling the blade margin in close proximity to the meristem. Blades with nests were 40%ushorter than blades lacking nests and reduced in area by 55%. We examined the composition of amphipods inhabiting eachunest to assess the temporal persistence of grazer aggregations. Nests were occupied by a single female or male–female pairs, and their newly hatched offspring. Analysis of offspring size distributions suggested that offspring dispersed from the maternal nest and did not remain to breed themselves. By concentrating physical damage and feeding on valuable tissues, these results indicate that even low numbers of small herbivores can cause localized impacts on the morphology and size of fast-growing algal blades. Predicting the consequences of this damage on larger scales will require understanding the spatial and temporal distribution of amphipod nests on giant kelp.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Location Call Number Limitation Availability
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