GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 2010-2014  (46)
Document type
Keywords
Language
Years
Year
  • 1
    Keywords: Hochschulschrift
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (144 Blatt = 4 MB) , Illustrationen, Diagramme
    Language: English
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Lebrato, Mario; Molinero, Juan-Carlos; Cartes, Joan E; Lloris, Domingo; Melin, Frederic; Beni-Casadella, Laia (2013): Sinking Jelly-Carbon Unveils Potential Environmental Variability along a Continental Margin. PLoS ONE, 8(12), e82070, https://doi.org/10.1371/journal.pone.0082070
    Publication Date: 2023-10-28
    Description: Particulate matter export fuels benthic ecosystems in continental margins and the deep sea, removing carbon from the upper ocean. Gelatinous zooplankton biomass provides a fast carbon vector that has been poorly studied. Observational data of a large-scale benthic trawling survey from 1994 to 2005 provided a unique opportunity to quantify jelly-carbon along an entire continental margin in the Mediterranean Sea and to assess potential links with biological and physical variables. Biomass depositions were sampled in shelves, slopes and canyons with peaks above 1000 carcasses per trawl, translating to standing stock values between 0.3 and 1.4 mg C m2 after trawling and integrating between 30,000 and 175,000 m2 of seabed. The benthopelagic jelly-carbon spatial distribution from the shelf to the canyons may be explained by atmospheric forcing related with NAO events and dense shelf water cascading, which are both known from the open Mediterranean. Over the decadal scale, we show that the jelly-carbon depositions temporal variability paralleled hydroclimate modifications, and that the enhanced jelly-carbon deposits are connected to a temperature-driven system where chlorophyll plays a minor role. Our results highlight the importance of gelatinous groups as indicators of large-scale ecosystem change, where jelly-carbon depositions play an important role in carbon and energy transport to benthic systems.
    Keywords: Abundance; Abundance per area; Area; Area/locality; Biomass; Biomass as carbon per area; Biomass as nitrogen per area; Bottom trawl; BT; Carbon, organic, particulate; Climate - Biogeochemistry Interactions in the Tropical Ocean; Cornide_1994_81; Cornide_1994_82; Cornide_1995_2; Cornide_1995_30; Cornide_1995_36; Cornide_1995_38; Cornide_1995_39; Cornide_1995_48; Cornide_1995_50; Cornide_1995_51; Cornide_1995_53; Cornide_1995_54; Cornide_1995_55; Cornide_1995_70; Cornide_1995_71; Cornide_1996_105; Cornide_1996_106; Cornide_1996_12; Cornide_1996_18; Cornide_1996_20; Cornide_1996_24; Cornide_1996_31; Cornide_1996_32; Cornide_1996_33; Cornide_1996_34; Cornide_1996_35; Cornide_1996_36; Cornide_1996_37; Cornide_1996_38; Cornide_1996_39; Cornide_1996_41; Cornide_1996_42; Cornide_1996_43; Cornide_1996_50; Cornide_1996_52; Cornide_1996_53; Cornide_1996_54; Cornide_1996_55; Cornide_1996_56; Cornide_1996_57; Cornide_1996_58; Cornide_1996_59; Cornide_1996_60; Cornide_1996_62; Cornide_1996_63; Cornide_1996_64; Cornide_1996_67; Cornide_1996_73; Cornide_1996_74; Cornide_1996_75; Cornide_1996_76; Cornide_1996_78; Cornide_1996_79; Cornide_1996_80; Cornide_1996_83; Cornide_1997_102; Cornide_1997_53; Cornide_1997_54; Cornide_1997_56; Cornide_1997_68; Cornide_1997_73; Cornide_1997_74; Cornide_1997_75; Cornide_1997_78; Cornide_1997_81; Cornide_1998_11; Cornide_1998_12; Cornide_1998_14; Cornide_1998_19; Cornide_1998_48; Cornide_1998_6; Cornide_1999_32; Cornide_1999_47; Cornide_1999_56; Cornide_1999_81; Cornide_2000_10; Cornide_2000_19; Cornide_2000_36; Cornide_2000_6; Cornide_2000_84; Cornide_2000_91; Cornide_2001_106; Cornide_2001_107; Cornide_2001_108; Cornide_2001_11; Cornide_2001_18; Cornide_2001_30; Cornide_2001_32; Cornide_2001_41; Cornide_2001_42; Cornide_2001_43; Cornide_2001_44; Cornide_2001_5; Cornide_2001_51; Cornide_2001_55; Cornide_2001_63; Cornide_2001_64; Cornide_2001_69; Cornide_2001_71; Cornide_2001_85; Cornide_2001_86; Cornide_2002_10; Cornide_2002_100; Cornide_2002_103; Cornide_2002_104; Cornide_2002_105; Cornide_2002_106; Cornide_2002_108; Cornide_2002_110; Cornide_2002_111; Cornide_2002_114; Cornide_2002_115; Cornide_2002_116; Cornide_2002_117; Cornide_2002_118; Cornide_2002_119; Cornide_2002_120; Cornide_2002_21; Cornide_2002_22; Cornide_2002_23; Cornide_2002_24; Cornide_2002_34; Cornide_2002_50; Cornide_2002_58; Cornide_2002_62; Cornide_2002_63; Cornide_2002_72; Cornide_2002_73; Cornide_2002_75; Cornide_2002_78; Cornide_2002_98; Cornide_2003_10; Cornide_2003_100; Cornide_2003_101; Cornide_2003_104; Cornide_2003_105; Cornide_2003_106; Cornide_2003_107; Cornide_2003_108; Cornide_2003_109; Cornide_2003_11; Cornide_2003_111; Cornide_2003_114; Cornide_2003_115; Cornide_2003_12; Cornide_2003_13; Cornide_2003_15; Cornide_2003_18; Cornide_2003_23; Cornide_2003_24; Cornide_2003_26; Cornide_2003_27; Cornide_2003_28; Cornide_2003_4; Cornide_2003_44; Cornide_2003_45; Cornide_2003_46; Cornide_2003_47; Cornide_2003_48; Cornide_2003_49; Cornide_2003_50; Cornide_2003_51; Cornide_2003_52; Cornide_2003_53; Cornide_2003_54; Cornide_2003_55; Cornide_2003_56; Cornide_2003_57; Cornide_2003_58; Cornide_2003_6; Cornide_2003_68; Cornide_2003_69; Cornide_2003_70; Cornide_2003_71; Cornide_2003_72; Cornide_2003_73; Cornide_2003_74; Cornide_2003_75; Cornide_2003_76; Cornide_2003_77; Cornide_2003_78; Cornide_2003_79; Cornide_2003_8; Cornide_2003_80; Cornide_2003_81; Cornide_2003_82; Cornide_2003_83; Cornide_2003_84; Cornide_2003_86; Cornide_2003_87; Cornide_2003_89; Cornide_2003_90; Cornide_2003_91; Cornide_2003_92; Cornide_2003_93; Cornide_2003_94; Cornide_2003_95; Cornide_2003_96; Cornide_2003_97; Cornide_2004_100; Cornide_2004_107; Cornide_2004_108; Cornide_2004_122; Cornide_2004_15; Cornide_2004_23; Cornide_2004_27; Cornide_2004_28; Cornide_2004_29; Cornide_2004_30; Cornide_2004_32; Cornide_2004_33; Cornide_2004_34; Cornide_2004_37; Cornide_2004_38; Cornide_2004_39; Cornide_2004_40; Cornide_2004_43; Cornide_2004_44; Cornide_2004_47; Cornide_2004_48; Cornide_2004_49; Cornide_2004_51; Cornide_2004_52; Cornide_2004_53; Cornide_2004_54; Cornide_2004_55; Cornide_2004_56; Cornide_2004_57; Cornide_2004_58; Cornide_2004_60; Cornide_2004_61; Cornide_2004_67; Cornide_2004_68; Cornide_2004_70; Cornide_2004_75; Cornide_2004_76; Cornide_2004_84; Cornide_2004_85; Cornide_2004_86; Cornide_2004_89; Cornide_2004_90; Cornide_2005_36; Cornide_2005_54; Cornide_2005_67; Cornide_2005_68; Cornide_2005_74; Cornide_2005_89; Dry mass; Event label; Height; Length; Nitrogen, organic, particulate; Sector; SFB754; Speed; Volume; Wet mass
    Type: Dataset
    Format: text/tab-separated-values, 4446 data points
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2019-10-21
    Description: We investigated potential connections over the past 2 decades between mesoscale circulation regimes in the Ionian Sea and newly-observed species and the concurrent rise in sea temperature in the Adriatic Sea. Analyses of plankton samples from 1993 to 2011 in the southern Adriatic revealed marked changes in the non-crustacean zooplankton community. Eleven species were recorded for the first time in the Adriatic, while 3 species reappeared after years of absence. We found that pluriannual changes in the zooplankton community tracked the continuum of circulation regimes in the Northern Ionian Gyre (NIG). The occurrence of Atlantic/Western Mediterranean species coincided with anti-cyclonic circulation in the NIG, probably due to the advection of Modified Atlantic Water into the Adriatic, while the presence of Lessepsian species coincided with the cyclonic pattern, which governs the entry of Eastern Mediterranean waters. The impact has been that newcomers now make a significant contribution to the zooplankton community in the southern Adriatic and, in certain cases, have replaced native species. Our results provide new evidence of the influence of teleconnection processes between the North Atlantic and Eastern Mediterranean on the dynamics of water masses in the southern Adriatic. The synergistic effects of these processes, together with warmer Mediterranean waters, raise concerns over dramatic changes in the marine biodiversity of the Adriatic.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2018-06-06
    Description: The diatom Thalassiosira minima was first recorded in the Baha Blanca Estuary in 1992. In 19921993 it exhibited a broad seasonal occurrence. A recent survey (20062007) showed a seasonal appearance restricted mainly to summer together with a greater relative abundance within the phytoplankton. A close connection was found with warmer, more saline and highly turbid conditions experienced in recent summers in the estuary. Whether these changes will impact the estuary trophic dynamics remains an open question.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2019-01-21
    Description: Aurelia aurita s.l. is the most widespread scyphozoan jellyfish that recurrently appear "en mass" and forms large aggregations mainly in coastal waters, embayments and estuaries. Beside anthropogenic factors controlling jellyfish populations climate change may play an important role. The aim of this study was to assess whether climate-related factors in absence of other anthropogenically induced stressor influence medusae size. We investigated seasonal and interannual changes in the size of Aurelia in a "jelly lake" in the National Park of Mljet Island (Croatia) where minimal human impact on the environment makes the Veliko Jezero a natural mesocosm for understanding the impact of climate change on the Aurelia population. The observed changes suggest Aurelia medusa population response to changing environment, in particular to enhanced temperature, by reduced body sizes. Comparison of Aurelia population dynamics from different regions in the Mediterranean Sea revealed the unique feature of the Veliko Jezero population. Despite the similarity of the environmental windows of medusae occurrences in the Veliko Jezero and regions in the Mediterranean Sea, medusae in the Veliko Jezero are present all year round. It seems that the lake bathymetry enables medusae to vertically migrate to deeper and cooler water layer, avoiding the limiting temperatures developed in the upper layer during the summer. These conditions may prolong the Aurelia medusae life span and together with continuous strobilation support the stability of the Aurelia medusae population all year round.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    facet.materialart.
    Unknown
    Oxford University Press
    In:  Journal of Plankton Research, 35 (3). pp. 677-683.
    Publication Date: 2019-01-22
    Description: We investigated the gelatinous carnivore zooplankton community in the coastal waters of northeast Taiwan during the period 20072010. The community assemblage was composed of 45 species, of which only 14 appeared recurrent in Taiwanese waters. Although there was no clear seasonality, higher richness and abundances occurred in spring and autumn. Examination of potential physical drivers of coastal biomass accumulation did not show any link with water mass transport; instead, peak events were associated with typhoon disturbances, suggesting a potential resource pulse effect.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2017-06-22
    Description: Particulate matter export fuels benthic ecosystems in continental margins and the deep sea, removing carbon from the upper ocean. Gelatinous zooplankton biomass provides a fast carbon vector that has been poorly studied. Observational data of a large-scale benthic trawling survey from 1994 to 2005 provided a unique opportunity to quantify jelly-carbon along an entire continental margin in the Mediterranean Sea and to assess potential links with biological and physical variables. Biomass depositions were sampled in shelves, slopes and canyons with peaks above 1000 carcasses per trawl, translating to standing stock values between 0.3 and 1.4 mg C m2 after trawling and integrating between 30,000 and 175,000 m2 of seabed. The benthopelagic jelly-carbon spatial distribution from the shelf to the canyons may be explained by atmospheric forcing related with NAO events and dense shelf water cascading, which are both known from the open Mediterranean. Over the decadal scale, we show that the jelly-carbon depositions temporal variability paralleled hydroclimate modifications, and that the enhanced jelly-carbon deposits are connected to a temperature-driven system where chlorophyll plays a minor role. Our results highlight the importance of gelatinous groups as indicators of large-scale ecosystem change, where jelly-carbon depositions play an important role in carbon and energy transport to benthic systems.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2017-09-14
    Description: The relative roles of temperature and food availability on the seasonal and daily growth of whitefish Coregonus lavaretus larvae were investigated in the oligotrophic peri-alpine Lake Annecy, France. During the spring from 2004 to 2007, surface water temperature and density of potential zooplankton prey were monitored, and 2688 larvae were caught and measured. In addition, the daily growth of 130 larvae was estimated retrospectively by investigating the microstructure of their otoliths. Temperature played the predominant role in controlling both seasonal and daily growth of early larvae. In contrast, the abundance of Mesocyclops leuckarti and larval density was only slightly correlated to larval growth, suggesting no food limitation nor strong interindividual competition over the study period. Overall, these findings run counter to concerns about potential food limitation, but sound a warning about the potential impact of climate change on fish ecology and fisheries management.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2019-01-21
    Description: The seasonal succession of plankton is an annually repeated process of community assembly during which all major external factors and internal interactions shaping communities can be studied. A quarter of a century ago, the state of this understanding was described by the verbal plankton ecology group (PEG) model. It emphasized the role of physical factors, grazing and nutrient limitation for phytoplankton, and the role of food limitation and fish predation for zooplankton. Although originally targeted at lake ecosystems, it was also adopted by marine plankton ecologists. Since then, a suite of ecological interactions previously underestimated in importance have become research foci: overwintering of key organisms, the microbial food web, parasitism, and food quality as a limiting factor and an extended role of higher order predators. A review of the impact of these novel interactions on plankton seasonal succession reveals limited effects on gross seasonal biomass patterns, but strong effects on species replacements.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    facet.materialart.
    Unknown
    Elsevier
    In:  Marine Environmental Research, 89 . pp. 91-96.
    Publication Date: 2017-08-23
    Description: We examined plankton responses to climate variance by using high temporal resolution data from 1988 to 2007 in the Western English Channel. Climate variability modified both the magnitude and length of the seasonal signal of sea surface temperature, as well as the timing and depth of the thermocline. These changes permeated the pelagic system yielding conspicuous modifications in the phenology of autotroph communities and zooplankton. The climate variance envelope, thus far little considered in climate-plankton studies, is closely coupled with the non-stationary dynamics of plankton, and sheds light on impending ecological shifts and plankton structural changes. Our study calls for the integration of the non-stationary relationship between climate and plankton in prognostic models on the productivity of marine ecosystems
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...