This dataset gathers isotopic ratios (carbon and nitrogen) and concentrations of both priority (mercury species and polychlorinated biphenyls congeners) and emerging (musks and sunscreens) micropollutants measured in a host-parasite couple (hake Merluccius merluccius muscle and in its parasite Anisakis sp) from the south of Bay of Biscay in 2018. In addition, the hake infection degree measured as the number of Anisakis sp. larvae was added for each hake collected.

A prerequisite for a successful development of a multi-mission wind dataset is to ensure good inter-calibration of the different extreme wind datasets to be integrated in the product. Since the operational hurricane community is working with the in-situ dropsondes as wind speed reference, which are in turn used to calibrate the NOAA Hurricane Hunter Stepped Frequency Microwave Radiometer (SFMR) wind data, MAXSS has used the latter to ensure extreme-wind inter-calibration among the following scatterometer and radiometer systems: the Advanced Scatterometers onboard the Metop series (i.e., ASCAT-A, -B, and -C), the scatterometers onboard Oceansat-2 (OSCAT) and ScatSat-1 (OSCAT-2), and onboard the HY-2 series (HSCAT-A, -B); the Advanced Microwave Scanning Radiometer 2 onboard GCOM-W1(AMSR-2), the multi-frequency polarimetric radiometer (Windsat), and the L-band radiometers onboard the Soil Moisture and Ocean Salinity (SMOS) and the Soil Moisture Active Passive (SMAP) missions. In summary, a two-step strategy has been followed to adjust the high and extreme wind speeds derived from the mentioned scatterometer and radiometer systems, available in the period 2009-2020. First, the C-band ASCATs have been adjusted against collocated storm-motion centric SFMR wind data. Then, both SFMR winds and ASCAT adjusted winds have been used to adjust all the other satellite wind systems. In doing so, a good inter-calibration between all the systems is ensured not only under tropical cyclone (TC) conditions, but also elsewhere. This dataset was produced in the frame of the ESA funded Marine Atmosphere eXtreme Satellite Synergy (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.

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.

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.

In recent years, large datasets of in situ marine carbonate system parameters (partial pressure of CO2 (pCO2), total alkalinity, dissolved inorganic carbon and pH) have been collated. These carbonate system datasets have highly variable data density in both space and time, especially in the case of pCO2, which is routinely measured at high frequency using underway measuring systems. This variation in data density can create biases when the data are used, for example for algorithm assessment, favouring datasets or regions with high data density. A common way to overcome data density issues is to bin the data into cells of equal latitude and longitude extent. This leads to bins with spatial areas that are latitude and projection dependent (eg become smaller and more elongated as the poles are approached). Additionally, as bin boundaries are defined without reference to the spatial distribution of the data or to geographical features, data clusters may be divided sub-optimally (eg a bin covering a region with a strong gradient). To overcome these problems and to provide a tool for matching in situ data with satellite, model and climatological data, which often have very different spatiotemporal scales both from the in situ data and from each other, a methodology has been created to group in situ data into ‘regions of interest’, spatiotemporal cylinders consisting of circles on the Earth’s surface extending over a period of time. These regions of interest are optimally adjusted to contain as many in situ measurements as possible. All in situ measurements of the same parameter contained in a region of interest are collated, including estimated uncertainties and regional summary statistics. The same grouping is done for each of the other datasets, producing a dataset of matchups. About 35 million in situ datapoints were then matched with data from five satellite sources and five model and re-analysis datasets to produce a global matchup dataset of carbonate system data, consisting of 287,000 regions of interest spanning 54 years from 1957 to 2020. Each region of interest is 100 km in diameter and 10 days in duration. An example application, the reparameterisation of a global total alkalinity algorithm, is shown. This matchup dataset can be updated as and when in situ and other datasets are updated, and similar datasets at finer spatiotemporal scale can be constructed, for example to enable regional studies. This dataset was funded by ESA Satellite Oceanographic Datasets for Acidification (OceanSODA) project which aims at developing the use of satellite Earth Observation for studying and monitoring marine carbonate chemistry.

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.

In order to better characterize the genetic diversity of Cetaceans and especially the common Dolphin from the Bay of Biscay, sequences from the mitochondrial Cytochrome B 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 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).

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 4 (L4) data) with a particular focus for use in climate studies. This dataset contains the Version 3 Remote Sensing Significant Wave Height product, gridded over a global regular cylindrical projection (1°x1° resolution), averaging valid and good measurements from all available altimeters on a monthly basis (using the L2P products also available). These L4 products are meant for statistics and visualization. The altimeter data used in the Sea State CCI dataset v3 come from multiple satellite missions spanning from 2002 to 2021 ( 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).

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