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).

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.

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.

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.

This dataset provides Level 4 total current including geostrophy and a data-driven approach for Ekman and near-inertial current, based on a convolution between drifter observation and wind history, to fit empirically a complex and time-lag dependant transfert function between ERA5 wind stress and current 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 Datlas and is distributed by Ifremer / CERSAT in the frame of the World Ocean Circulation (WOC) project funded by the European Space Agency (ESA).

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.

The GEBCO_2022 Grid is a global continuous terrain model for ocean and land with a spatial resolution of 15 arc seconds. In regions outside of the Arctic Ocean area, the grid uses as a base Version 2.4 of the SRTM15_plus data set (Tozer, B. et al, 2019). This data set is a fusion of land topography with measured and estimated seafloor topography. Included on top of this base grid are gridded bathymetric data sets developed by the four Regional Centers of The Nippon Foundation-GEBCO Seabed 2030 Project. The GEBCO_2022 Grid represents all data within the 2022 compilation. The compilation of the GEBCO_2022 Grid was carried out at the Seabed 2030 Global Center, hosted at the National Oceanography Centre, UK, with the aim of producing a seamless global terrain model. Outside of Polar regions, the Regional Centers provide their data sets as sparse grids i.e. only grid cells that contain data are populated. These data sets were included on to the base using a remove-restore blending procedure. This is a two-stage process of computing the difference between the new data and the base grid and then gridding the difference and adding the difference back to the existing base grid. The aim is to achieve a smooth transition between the new and base data sets with the minimum of perturbation of the existing base data set. The data sets supplied in the form of complete grids (primarily areas north of 60N and south of 50S) were included using feather blending techniques from GlobalMapper software. The GEBCO_2022 Grid has been developed through the Nippon Foundation-GEBCO Seabed 2030 Project. This is a collaborative project between the Nippon Foundation of Japan and the General Bathymetric Chart of the Oceans (GEBCO). It aims to bring together all available bathymetric data to produce the definitive map of the world ocean floor by 2030 and make it available to all. Funded by the Nippon Foundation, the four Seabed 2030 Regional Centers include the Southern Ocean - hosted at the Alfred Wegener Institute, Germany; South and West Pacific Ocean - hosted at the National Institute of Water and Atmospheric Research, New Zealand; Atlantic and Indian Oceans - hosted at the Lamont-Doherty Earth Observatory, Columbia University, USA; Arctic and North Pacific Oceans - hosted at Stockholm University, Sweden and the Center for Coastal and Ocean Mapping at the University of New Hampshire, USA.

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

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.

The ESA Sea State Climate Change Initiative (CCI) project has produced global daily merged multi-sensor time-series of along-track satellite altimeter significant wave height data (referred to as Level 3 (L3) 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. It has been generated from upstream Sea State CCI L2P products, edited and merged into daily products, retaining only valid and good quality measurements from all altimeters over one day, with simplified content (only a few key parameters). This is close to what is delivered in Near-Real Time by the CMEMS (Copernicus - Marine Environment Monitoring Service) project. It covers the date range from 2002-2021. The altimeter data used in the Sea State CCI dataset v3 come from multiple satellite missions (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).