2022
Type of resources
Available actions
Topics
Keywords
Contact for the resource
Provided by
Years
Formats
Representation types
Update frequencies
status
Service types
Scale
Resolution
-
In order to better characterize the genetic diversity of Cetaceans and especially the common Dolphin from the Bay of Biscay, sequences from the variable mitochondrial control region were obtained from water samples acquired close to groups of dolphins.
-
The ESA Sea State Climate Change Initiative (CCI) project has produced global multi-sensor time-series of along-track satellite altimeter significant wave height data (referred to as Level 2P (L2P) data) with a particular focus for use in climate studies. This dataset contains the Version 3 Remote Sensing Significant Wave Height product, which provides along-track data at approximately 6 km spatial resolution, separated per satellite and pass, including all measurements with flags, corrections and extra parameters from other sources. These are expert products with rich content and no data loss. The altimeter data used in the Sea State CCI dataset v3 come from multiple satellite missions spanning from 2002 to 2022021 (Envisat, CryoSat-2, Jason-1, Jason-2, Jason-3, SARAL, Sentinel-3A), therefore spanning over a shorter time range than version 1.1. Unlike version 1.1, this version 3 involved a complete and consistent retracking of all the included altimeters. Many altimeters are bi-frequency (Ku-C or Ku-S) and only measurements in Ku band were used, for consistency reasons, being available on each altimeter but SARAL (Ka band).
-
The upper ocean pycnocline (UOP) monthly climatology is based on the ISAS20 ARGO dataset containing Argo and Deep-Argo temperature and salinity profiles on the period 2002-2020. Regardless of the season, the UOP is defined as the shallowest significant stratification peak captured by the method described in Sérazin et al. (2022), whose detection threshold is proportional to the standard deviation of the stratification profile. The three main characteristics of the UOP are provided -- intensity, depth and thickness -- along with hydrographic variables at the upper and lower edges of the pycnocline, the Turner angle and density ratio at the depth of the UOP. A stratification index (SI) that evaluates the amount of buoyancy required to destratify the upper ocean down to a certain depth, is also included. When evaluated at the bottom of the UOP, this gives the upper ocean stratification index (UOSI) as discussed in Sérazin et al. (2022). Three mixed layer depth variables are also included in this dataset, including the one using the classic density threshold of 0.03 kg.m-3, along with the minimum of these MLD variables. Several statistics of the UOP characteristics and the associated quantities are available in 2°×2° bins for each month of the year, whose results were smoothed using a diffusive gaussian filter with a 500 km scale. UOP characteristics are also available for each profile, with all the profiles sorted in one file per month.
-
WGS for Iatlantic projet ( ) for assessing past and present connectivity
-
This dataset consists of metatranscriptomic sequencing reads corresponding to coastal micro-eukaryote communities sampled in Western Europe in 2018 and 2019.
-
New results acquired in south-Brittany (MD08-3204 CQ core: Bay of Quiberon and VK03-58bis core: south Glénan islands) allow depicting Holocene paleoenvironmental changes from 8.5 ka BP to present through a multi-proxy dataset including sedimentological and palynological data. First, grain-size analyses and AMS-14C dates highlight a common sedimentary history for both study cores. The relative sea level (RSL) slowdown was accompanied by a significant drop of the sedimentation rates between ca. 8.3 and 5.7 ka BP, after being relatively higher at the onset of the Holocene. This interval led to the establishment of a shell-condensed level, identified in core VK03-58bis by the “Turritella layer” and interpreted as a marker for the maximum flooding surface. Palynological data (pollen grains and dinoflagellate cyst assemblages) acquired in core MD08-3204 CQ argue for an amplification of the fluvial influence since 5.7 ka BP; the establishment of the highstand system tract (i.e., mixed marine and fluviatile influences on the platform) then accompanying the slowdown of the RSL rise-rates. On the shelf, the amplification of Anthropogenic Pollen Indicators (API) is then better detected since 4.2 ka BP, not only due to human impact increase but also due to a stronger fluvial influence on the shelf during the Late Holocene. Palynological data, recorded on the 8.5–8.3 ka BP interval along an inshore-offshore gradient, also demonstrate the complexity of the palynological signal such as i) the fluvial influence that promotes some pollinic taxa (i.e., Corylus, Alnus) from proximal areas and ii) the macro-regionalization of palynomorph sources in distal cores. In addition, the comparison of palynological tracers, including API, over the last 7 kyrs, with south-Brittany coastal and mid-shelf sites subjected to northern vs. southern Loire catchment areas, allowed discussing a major hydro-climatic effect on the reconstructed palynological signals. Strengthened subpolar gyre dynamics (SPG), combined with recurrent positive North Atlantic Oscillation (NAO) configurations, appear responsible for increased winter precipitations and fluvial discharges over northern Europe, such as in Brittany. Conversely, weakened SPG intervals, associated with negative NAO-like modes, are characterized by intensified winter fluvial discharges over southern Europe. Interestingly, we record, at an infra-orbital timescale, major peaks of API during periods of strengthened (/weakened) SPG dynamics in sites subjects to Brittany watersheds (/Loire watersheds) inputs.
-
Raw reads for the assembly of Gambusia holbrooki genome.
-
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.
-
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
Catalogue PIGMA