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2022

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  • 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).

  • 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.

  • The SWISCA Level 2S (L2S) product provides along-track colocation of SWIM wave measuring instrument onto SCAT scatterometer grid, over the global ocean. SWIM and SCAT are both instruments onboard CFOSAT. CFOSAT (Chinese French Ocean SATellite) is a french-chinese mission launched in 2018, whose aim is to provide wind (SCAT instrument) and wave (SWIM instrument) measurements over the sea surface. The SWISCA L2S product is broken down into three different subproducts: - L2A containing the sigma0 of both SWIM and SCAT - L2B containing the wave parameters measured by SWIM and wind vectors measured by SCAT - AUX containing additional ancillary fields such as sea ice concentration (from CERSAT/SSMI), ocean currents (from CMEMS/GlobCurrent), SST and Wind (from ECMWF), rain rate (from IMERG), and WaveWatch3 wave spectra. All SWIM and ancillary observations are resampled onto SCAT scatterometer's geometry (wind vector cells, WVC). The SWISCA level 2S product is generated in delayed mode, a few days after acquisition. It is intended to foster cross analysis of SWIM and SCAT observations, and their combination to improve the retrieval of both wind and wave parameters. The SWISCA L2S product is generated and distributed by Ifremer / CERSAT in the frame of the Ifremer Wind and Wave Operation Center (IWWOC) co-funded by Ifremer and CNES and dedicated to the processing of the delayed mode data of CFOSAT mission.

  • We genotyped 1680 thornback ray Raja clavata sampled in the Bay of Biscay using a DNA chip described in Le Cam et al. (2019). After quality control 4604 SNPs were retained for identifying potential sex-linked SNPs using three methods: i) identification of excess of heterozygotes in one sex, ii) FST outlier analysis between the two sexes and iii) neuronal net modelling. Genotype coding: 0 homozygous for major allele, 1 heterozygous, 2 homozygous for minor allele. Flanking DNA sequences of SNPs identified with methods i) and ii) are also provided.  

  • The CDR-derived Wet Tropospheric Correction (WTC) Product V2 is generated from the Level-2+ along-track altimetry products version 2024 (L2P 2024) distributed by AVISO+ (www.aviso.altimetry.fr). It provides a long-term, homogenized estimation of the wet tropospheric correction based on Climate Data Records (CDRs) of atmospheric water vapour combined with high frequencies MWR data. Two independent CDRs datasets are used: - REMSS V7R2 (coverage until 2022) https://www.remss.com/measurements/atmospheric-water-vapor/tpw-1-deg-product/ - HOAPS V5 precursor CDR from EUMETSAT CM SAF (coverage until 2020) HOAPS V4/V5 data available via https://wui.cmsaf.eu Note: the HOAPS V5 precursor is not yet an official CM SAF product; full validation and public release are pending. The MWR/CDR WTC V2 estimates is derived using spatially varying but temporally constant polynomial coefficients (ai). 1. WTC V2 – Along-track L2P Product Data format: The WTC V2 product is delivered in Level-2+ (L2P) format, along the satellite ground track. Each mission is distributed as a compressed archive (.tar.gz) containing one NetCDF4 CF-1.8 file per mission cycle. Archive naming convention: <mission>_WTC_from_WV_CDR_<version>.tar.gz mission: TP (TOPEX/Poseidon), J1, J2, J3 version: product version (currently V2) File naming convention inside archives: <mission>_C<cycle>.nc cycle: 4-digit cycle index (e.g., C0001) Each NetCDF file contains: 1/ Along-track WTC estimate; 2/ Ancillary information; 3/ Space–time coordinates 2. WTC CDR Uncertainties – Gridded Product: A complementary product is provided, delivering regional trend estimates and associated uncertainties from the WTC Climate Data Record. The uncertainty product is distributed as a single NetCDF4 file: wtc_trend_uncertainties.nc . This file contains global gridded fields of WTC CDR trend and uncertainty parameters. Product content: This is the first dedicated version providing both: WTC CDR (HOAPS) linear trends, and Uncertainty estimates on these trends. Uncertainties are expressed as 1-sigma confidence intervals, and propagated using the methodology described in Section 2.3 of the Product User Manual. The product includes: - Total uncertainty on the WTC trend, propagated from all identified uncertainty sources in the WTC–TCWV regression. - Individual contributions of uncertainty sources (Uncertainties on regression coefficients: a0, a1 and their standard deviations; Uncertainties inherited from the HOAPS TCWV CDR) These fields enable users to assess the relative importance of each uncertainty component and recompute uncertainty propagation with alternative methods. Included regression input variables: To ensure transparency and reproducibility, the product provides: 1/ regression coefficients a0, a1; 2/ their associated uncertainties (std of a0, std of a1); 3/additional diagnostic fields required to recompute uncertainties if needed.

  • 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.

  • 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.

  • 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.

  • The Mediterranean Sea is generally described as an oligotrophic area where primary productivity is limited to a few coastal environments with nutrient-enriched fluvial input. However, several studies have revealed that the hydrology of the western Mediterranean has major seasonal productive patterns linked either to significant riverine input or to seasonal upwelling cells. This study aims to: i) discuss organic microfossils (i.e. pollen and dinoflagellate cyst assemblages, as well as other non-pollen palynomorphs) from two different productive areas of the western Mediterranean Sea, and ii) examine the importance of the interconnections between marine and continental influences responsible for modern palynomorph distributions. Based on 25 samples from the Gulf of Lion (GoL) and Algerian Margin, this study key findings are: i) that GoL marine productivity is driven by the combination of discharges from the Rhône River and seasonal upwelling mechanisms, ii) that the strong productive pattern of the northern African coast is driven by water density front mixings and related upwellings. These two patterns are discussed in the light of major links that provide a better understanding of the signatures of marine and continental bio-indicators. The dinocyst Lingulodinium machaerophorum can be considered as a tracer of Rhône River plume influence in the GoL. Brigantedinium taxa are shown to be upwelling-sensitive in both studied areas. Typical differences in vegetation across the north–south climate gradient in the western Mediterranean Basin are highlighted by the larger ratio of Euro-Siberian to Mediterranean pollen taxa in the northern sector. Synoptic maps also illustrate the complex interactions of environmental drivers determining the distributions of continental and marine palynomorphs in the western Mediterranean Sea.