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2022

502 record(s)
 
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  • French Zostera Marina et Zostera Noltei abundance data are collected during monitoring surveys on the English Channel / Bay of Biscay coasts. Protocols are impletmented in the Water Framework Directive. Data are transmitted in a Seadatanet format (CDI + ODV) to EMODnet Biology european database. 35 ODV files have been generated from period 01/01/2004 to 31/12/2021 for Z. Marina and from 01/01/2011 to 31/12/2021 for Z. Noltei.  

  • The ESA Sea State Climate Change Initiative (CCI) project has produced global multi-sensor time-series of along-track satellite synthetic aperture radar (SAR) integrated sea state parameters (ISSP) data from ENVISAT (referred to as SAR Wave Mode onboard ENVISAT Level 2P (L2P) ISSP data) with a particular focus for use in climate studies. This dataset contains the ENVISAT Remote Sensing Integrated Sea State Parameter product (version 1.1), which forms part of the ESA Sea State CCI version 3.0 release. This product provides along-track significant wave height (SWH) measurements at 5km resolution every 100km, processed using the Li et al., 2020 empirical model, separated per satellite and pass, including all measurements with flags and uncertainty estimates. These are expert products with rich content and no data loss. The SAR Wave Mode data used in the Sea State CCI SAR WV onboard ENVISAT Level 2P (L2P) ISSP v3 dataset come from the ENVISAT satellite mission spanning from 2002 to 2012.

  • Serveur wms du projet CHARM II

  • The ESA Sea State Climate Change Initiative (CCI) project has produced global multi-sensor time-series of along-track satellite synthetic aperture radar (SAR) integrated sea state parameters (ISSP) data from Sentinel-1 (referred to as SAR WV onboard Sentinel-1 Level 2P (L2P) ISSP data) with a particular focus for use in climate studies. This dataset contains the Sentinel-1 SAR Remote Sensing Integrated Sea State Parameter product (v1.0), which forms part of the ESA Sea State CCI version 3.0 release. This product provides along-track primary significant wave height measurements and secondary sea state parameters, calibrated with CMEMS model data and reference in situ measurements at 20km resolution every 100km, processed using the Pleskachevsky et. al., 2021 emprical model, separated per satellite and pass, including all measurements with flags and uncertainty estimates. These are expert products with rich content and no data loss. The SAR Wave Mode data used in the Sea State CCI SAR WV onboard Sentinel-1 Level 2P (L2P) ISSP v3 dataset come from the Sentinel-1 satellite missions spanning from 2014 to 2021 (Sentinel-1 A, Sentinel-1 B).

  • Global wave hindcast (1961-2020) at 1° resolution using CMIP6 wind and sea-ice forcings for ALL (historical), GHG (historical greenhouse-gas-only), AER (historical Anthropogenic-aerosol-only), NAT (historical natural only) scenario.

  • This dataset consists of metatranscriptomic sequencing reads corresponding to coastal micro-eukaryote communities sampled in Western Europe in 2018 and 2019.

  • French intertidal and subtidal Macroalgae taxa data are collected during monitoring surveys on the English Channel / Bay of Biscay coasts.  Protocols are implemented in the Water Framework Directive. Data are transmitted in a Seadatanet format (CDI + ODV) to EMODnet Biology european database. 131 ODV files have been generated from period 01/01/2006 to 31/12/2021.

  • Particularly suited to the purpose of measuring the sensitivity of benthic communities to trawling, a trawl disturbance indicator (de Juan and Demestre, 2012, de Juan et al. 2009) was proposed based on benthic species biological traits to evaluate the sensibility of mega- and epifaunal community to fishing pressure known to have a physical impact on the seafloor (such as dredging and bottom trawling). The selected biological traits were chosen as they determine vulnerability to trawling: mobility, fragility, position on substrata, average size and feeding mode that can easily be related to the fragility, recoverability and vulnerability ecological concepts. The five categories retained are functional traits that were selected based on the knowledge of the response of benthic taxa to trawling disturbance (de Juan et al., 2009). They reflect respectively the possibility to avoid direct gear impact, to benefit from trawling for feeding, to escape gear, to get caught by the net and to resist trawling/dredging action, each of these characteristics being either advantageous or sensitive to trawling. To expand this approach to that proposed by Certain et al. (2015), the protection status of certain species was also indicated. To enable quantitative analysis, a score was assigned to each category: from low sensitivity (0) to high sensitivity (3). Biological traits of species have been defined, from the BIOTIC database (MARLIN, 2014) and from information given by Garcia (2010), Le Pape et al. (2007) and Brind’Amour et al. (2009). For missing traits, additional information from literature has been considered. The protection status of each taxa was also scored: Atlantic species listed in OSPAR List of Threatened and/or Declining Species and Habitats (https://www.ospar.org/work-areas/bdc/species-habitats/list-of-threatened-declining-species-habitats) and Mediterranean species listed in Vulnerable Marine Ecosystems (FAO, 2018 and Oceana, 2017) were scored 3 and other species were scored 1. The scores of 1085 taxa commonly found in bottom trawl by-catch in the southern North Sea, English Channel and north-western Mediterranean were described.

  • Reef-building species are recognized as having an important ecological role and as generally enhancing the diversity of benthic organisms in marine habitats.  However, although these ecosystem engineers have a facilitating role for some species, they may exclude or compete with others. The honeycomb worm Sabellaria alveolata (Linnaeus, 1767) is an important foundation species, commonly found from northwest Ireland to northern Mauritania (Curd et al., 2020), whose reef structures increase the physical complexity of the marine benthos, supporting high levels of biodiversity. Local patterns and regional differences in taxonomic and functional diversity were examined in honeycomb worm reefs from ten sites along the northeastern Atlantic to explore variation in diversity across biogeographic regions and the potential effects of environmental drivers. To characterize the functional diversity at each site, a biological trait analysis (BTA) was conducted (Statzner et al., 1994). Here we present the functional trait database used for the benthic macrofauna found to live in association with honeycomb worm reefs. Eight biological traits (divided into 32 modalities) were selected (Table 1), providing information linked to the ecological functions performed by the associated macrofauna. The selected traits provide information on: (i) resource use and availability (by the trophic group of species, e.g. Thrush et al. 2006); (ii) secondary production and the amount of energy and organic matter (OM) produced based on the life cycle of the organisms (including longevity, maximum size and mode of reproduction, e.g. (Cusson and Bourget, 2005; Thrush et al., 2006) and; (iii) the behavior of the species in general [i.e. how these species occupy the environment and contribute to biogeochemical fluxes through habitat, movement, and bioturbation activity at different bathymetric levels, e.g. (Solan et al., 2004; Thrush et al., 2006; Queirós et al., 2013). Species were scored for each trait modality based on their affinity using a fuzzy coding approach (Chevenet et al., 1994), where multiple modalities can be attributed to a species if appropriate, and allowed for the incorporation of intraspecific variability in trait expression. The information concerning polychaetes was derived primarily from Fauchald et al (1979) and Jumars et al (2015). Information on other taxonomic groups was obtained either from databases of biological traits (www.marlin.ac.uk/biotic) or publications (Naylor, 1972; King, 1974; Caine, 1977; Lincoln, 1979; Holdich and Jones, 1983; Smaldon et al., 1993; Ingle, 1996; San Martín, 2003; Southward, 2008; Gil, 2011; Leblanc et al., 2011; Rumbold et al., 2012; San Martín and Worsfold, 2015; Jones et al., 2018). Map indicating the locations of the 10 study sites in the UK, France and Portugal within the four biogeographic provinces defined by Dinter (2001). (All sites were sampled in 8 different stations, except for UK4 where 5 stations were sampled).

  • Phenotypic plasticity, the ability of a single genotype to produce multiple phenotypes, is important for survival when species are faced with novel conditions. Theory predicts that range-edge populations will have greater phenotypic plasticity than core populations, but empirical examples from the wild are rare. The honeycomb worm, Sabellaria alveolata (L.), constructs the largest biogenic reefs in Europe, which support high biodiversity and numerous ecological functions. In order to assess the presence, causes and consequences of intraspecific variation in developmental plasticity and thermal adaptation in the honeycomb worm, we carried out common-garden experiments using the larvae of individuals sampled from along a latitudinal gradient covering the entire range of the species. We exposed larvae to three temperature treatments and measured phenotypic traits throughout development. We found phenotypic plasticity in larval growth rate but local adaptation in terms of larval period. The northern and southern range-edge populations of S. alveolata showed phenotypic plasticity for growth rate: growth rate increased as temperature treatment increased. In contrast, the core range populations showed no evidence of phenotypic plasticity. We present a rare case of range-edge plasticity at both the northern and southern range limit of species, likely caused by evolution of phenotypic plasticity during range expansion and its maintenance in highly heterogeneous environments. This dataset presents the raw image data collected for larval stages of Sabellaria alveolata from 5 populations across Europe and Northern Africa, exposed to 15, 20 and 25 C. Included are also opercular crown measurements used to estimate de size classes of individuals present in each population.  All measurements made with the images collected are presented in an Excel spreadsheet, also available here.