Serveur wms du projet CHARM II

Understanding the dynamics of species interactions for food (prey-predator, competition for resources) and the functioning of trophic networks (dependence on trophic pathways, food chain flows, etc.) has become a thriving ecological research field in recent decades. This empirical knowledge is then used to develop population and ecosystem modelling approaches to support ecosystem-based management. The TrophicCS data set offers spatialized trophic information on a large spatial scale (the entire Celtic Sea continental shelf and upper slope) for a wide range of species. It combines ingested prey (gut content analysis) and a more integrated indicator of food sources (stable isotope analysis). A total of 1337 samples of large epifaunal invertebrates (bivalve mollusks and decapod crustaceans), zooplankton, fish and cephalopods, corresponding to 114 species, were collected and analyzed for stable isotope analysis of their carbon and nitrogen content. Sample size varied between taxa (from 1 to 52), with an average of 11.72 individuals sampled per species, and water depths ranged from 57 to 516 m. The gut contents of 1026 fish belonging to ten commercially important species: black anglerfish (Lophius budegassa), white anglerfish (Lophius piscatorius), blue whiting (Micromesistius poutassou), cod (Gadus morhua), haddock (Melanogrammus aeglefinus), hake (Merluccius merluccius), megrim (Lepidorhombus whiffiagonis), plaice (Pleuronectes platessa), sole (Solea solea) and whiting (Merlangius merlangus) were analyzed. The stomach content data set contains the occurrence of prey in stomach, identified to the lowest taxonomic level possible. To consider potential ontogenetic diet changes, a large size range was sampled. The TrophicCS data set was used to improve understanding of trophic relationships and ecosystem functioning in the Celtic Sea. When you use the data in your publication, we request that you cite this data paper. If you use the present data set (TrophicCS) for the majority of the data analyzed in your study, you may wish to consider inviting at least one author of the core team of this data paper to become a collaborator /coauthor of your paper.

Serveur wms sur les photos anciennes

This dataset provides detections of fronts derived from high resolution remote sensing SST observations by SEVIRI L3C from OSISAF over Western Europe region. The data are available through HTTP and FTP; access to the data is free and open. In order to be informed about changes and to help us keep track of data usage, we encourage users to register at: https://forms.ifremer.fr/lops-siam/access-to-esa-world-ocean-circulation-project-data/ This dataset was generated by OceanDataLab and is distributed by Ifremer / CERSAT in the frame of the World Ocean Circulation (WOC) project funded by the European Space Agency (ESA).

This dataset contains the pictures used for morphometric measurements, as well as the elemental compositon and production rates data, of planktonic Rhizaria. Specimens were collected in the bay of Villefranche-sur-Mer in May 2019 and during the P2107 cruise in the California Current in July-August 2021. Analyses of the data can be found at https://github.com/MnnLgt/Elemental_composition_Rhizaria.

Raw reads for the assembly of Gambusia holbrooki genome.

The Level 4 merged microwave wind product is a complete set of hourly global 10-m wind maps on a 0.25x0.25 degree latitude-longitude grid, spanning 1 Jan 2010 through the end of 2020. The product combines background neutral equivalent wind fields from ERA5, daily surface current fields from CMEMS, and stress equivalent winds obtained from several microwave passive and active sensors to produce hourly surface current relative stress equivalent wind analyses. The satellite winds include those from recently launched L-band passive sensors capable of measuring extreme winds in tropical cyclones, with little or no degradation from precipitation. All satellite winds used in the analyses have been recalibrated using a large set of collocated satellite-SFMR wind data in storm-centric coordinates. To maximize the use of the satellite microwave data, winds within a 24-hour window centered on the analysis time have been incorporated into each analysis. To accomodate the large time window, satellite wind speeds are transformed into deviations from ERA5 background wind speeds interpolated to the measurement times, and then an optical flow-based morphing technique is applied to these wind speed increments to propagate them from measurement to analysis time. These morphed wind speed increments are then added to the background wind speed at the analysis time to yield a set of total wind speeds fields for each sensor at the analysis time. These individual sensor wind speed fields are then combined with the background 10-m wind direction to yield vorticity and divergence fields for the individual sensor winds. From these, merged vorticity and divergence fields are computed as a weighted average of the individual vorticity and divergence fields. The final vector wind field is then obtained directly from these merged vorticity and divergence fields. Note that one consequence of producing the analyses in terms of vorticity and divergence is that there are no discontinuities in the wind speed fields at the (morphed) swath edges. There are two important points to be noted: the background ERA5 wind speed fields have been rescaled to be globally consistent with the recalibrated AMSR2 wind speeds. This rescaling involves a large increase in the ERA5 background winds beyond about 17 m/s. For example, an ERA5 10 m wind speed of 30 m/s is transformed into a wind speed of 41 m/s, and a wind speed of 34 m/s is transformed into a wind speed of about 48 m/s. Besides the current version of the product is calibrated for use within tropical cyclones and is not appropriate for use elsewhere. This dataset was produced in the frame of ESA MAXSS project. The primary objective of the ESA Marine Atmosphere eXtreme Satellite Synergy (MAXSS) project is to provide guidance and innovative methodologies to maximize the synergetic use of available Earth Observation data (satellite, in situ) to improve understanding about the multi-scale dynamical characteristics of extreme air-sea interaction.

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.

We developed a panel of single nucleotide polymorphism (SNP) markers for thornback ray Raja clavata using a RADSeq protocole. Demultiplexed sequences were aligned to the genome of Leucoraja erinacea which was used as reference genome. From an initial set of 389 483 putative SNPs, 7741 SNPs with the largest minor allele frequency were selected for implementation on an Infinium® XT iSelect-96 SNP-array implemented by LABOGENA DNA. For the array, SNPs [T/C] and [T/G] were replaced by those from the complementary strand [A/G] and [A/C] respectively. For some SNPs, a second SNP was found in the 50 nucleotide bases flanking sequence. In these cases, two SNP probes were developed with each of the two alleles of the second SNP. A SNP probe naming convention was adopted to identify these pairs of probes corresponding to the same SNP locus: “MAJ” or “MIN” followed by the corresponding base was included in the probe name. For some of these pairs, only one of the two markers could be developed, resulting in a total set of 9120 SNP probes, including 6360 single SNP probes, 10 MAJ or MIN probes for which a single probe was successfully developed, and 1375 pairs of probes with MAJ and MIN versions. The 9120 SNP genotypes were then scored using the clustering algorithm implemented in the Illumina® GenomeStudio Genotyping Analysis Module v2.0.3 for 7726 individual samples, including duplicates, mostly from the Bay of Biscay but also from the Mediterranean Sea and West Iberia. Overall, 1643 SNPs failed to be genotyped in all individuals, for 319 markers the minor allele was not found and 7158 markers (including 1974 for 987 MIN-MAJ pairs) produced bi-allelic genotypes. The majority of these SNPs had a minor allele frequency between 0.1 and 0.5. The MIN-MAJ probes can be used for quality checking the genotyping results

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.