The data sets presented here result from the long-term monitoring of individual growth patterns in anchovy and sardine in the Bay of Biscay, from 2000 to 2018. They derived from the PELGAS survey series (Doray et al., 2018), which monitors annually the Bay of Biscay pelagic ecosystem since 2000. The survey is performed in May during the peak spawning of anchovy and main spawning of sardine. Among the many data collected, anchovy and sardine populations are assessed by combining acoustic records with pelagic trawl hauls catches and ICES survey protocoles are used, as detailed in Doray et al. (2021). Briefly, fish acoustic backscatter are recorded along survey transect lines and pelagic trawl hauls undertaken opportunistically to identify echotraces to species and collect fish samples for acquiring biometric data. At each trawl haul and for each species, a random subsample of individuals is taken to establish the species’ length distributions. For anchovy and sardine, this subsample is further subsampled, spanning the whole length range, to take individual fish measurements. These amount to extracting otoliths and measuring individuals’ age, length, weight, sexual maturity and other parameters. Individual measurements are taken on fourty individuals of anchovy and sardine when the species are present in the catch. For each individual fish, the two otolith sagittae are extracted on board, mounted in leukit for age reading on board when permitting and/or on land in the laboratory. Growth patterns in the otoliths were analysed on land with a binocular stereomicroscope under reflected natural light. For anchovy, otoliths’ growth was measured for all individuals in all the hauls. For sardine, trawl hauls were selected and all individual otoliths were measured in each selected haul. The selection was made using the geographical stratification defined in Petitgas et al. (2018) based on the ecosystem spatial structure. An average of two to three hauls in each of the four strata were selected per year. The otoliths mounted in leukit were imaged and growth-at-age in the otoliths was measured with the software TNPC (Traitement numérique des pièces calcifiées: Mahé et al., 2009). Under the binocular microscope and natural light, the otoliths showed hyaline (aragonite-poor) rings corresponding to winter periods of low growth and between the rings, white opaque (aragonite-rich) portions corresponding to annual growth periods. The annual ring determination, the age assignment and the measurement of annual ring diameters followed ICES protocoles and guidelines for anchovy and sardine (ICES, 2010; 2011). The age was estimated as the number of hyaline rings. If the edge was hyaline, it was counted as a ring as a hyaline edge observed within the first half of the year is assumed to represent the last winter. The diameter of each annual ring was measured from middle of the hyaline ring on one side to the middle of the ring on the opposite side along the major elongated axis of the otolith and passing through its centre. The distance was expressed in mm after calibration of the stereomiscroscope and the pixel images. Such diameter corresponded to growth-at-age. Ages 0 to 4 were considered (diameters R1 to R5). The total diameter of the otolith was also measured. The data sets span 19 years, from 2000 to 2018 and comprise 20,186 and 8,624 individual fish analyzed at 535 and 235 trawl hauls for anchovy and sardine, respectively. These data sets were used by Boëns et al. (2021 and 2023) to analyse changes in growth patterns and growth-selective mortality at age in anchovy and sardine under environmental and fishing pressures. References: Doray, M., Boyra, G. and Van Der Kooij, J. (eds) (2021). ICES Survey Protocols – Manual for acoustic surveys coordinated under ICES Working Group on Acoustic and Egg Surveys for Small Pelagic Fish (WGACEGG). 1st Edition. ICES Techniques in Marine Environmental Sciences, 64. https://doi.org/10.17895/ices.pub.7462  Doray, M., Petitgas, P., Romagnan, J.-B., Huret, M., Duhamel, E., Dupuy, Ch., Spitz, J., Authier, M., Sanchez, F., Berger, L., Doremus, G., Bourriau, P., Grellier, P. and Masse, J. (2018). The PELGAS survey: ship-based integrated monitoring of the Bay of Biscay pelagic ecosystem. Progress In Oceanography, 166, 15-29. https://doi.org/10.1016/j.pocean.2017.09.015 ICES (2010). Report of the Workshop on Age reading of European anchovy (WKARA), 9-13 November 2009, Sicily, Italy. ICES CM 2009/ACOM: 43. 122 pp. https://doi.org/10.17895/ices.pub.19280525 ICES (2011). Report of the Workshop on Age Reading of European Atlantic Sardine (WKARAS), 14-18 February 2011, Lisbon, Portugal. ICES CM 2011/ACOM:42. 91 pp. https://doi.org/10.17895/ices.pub.19280855 Petitgas, P., Huret, M., Dupuy, Ch., Spitz, J., Authier, M., Romagnan, J.-B. and Doray, M. (2018). Ecosystem spatial structure revealed by integrated survey data. Progress In Oceanography, 166, 189-198. https://doi.org/10.1016/j.pocean.2017.09.012 Mahe, K., Bellail, R., Dufour, J.-L., Boiron-Leroy, A., Dimeet, J., Duhamel, E., Elleboode, R., Felix, J., Grellier, P., Huet, J., Labastie, J., Le Roy, D., Lizaud, O., Manten, M.-L., Martin, S., Metral, L., Nedelec, D., Verin, Y. and Badts, V. (2009). Synthèse française des procédures d'estimation d'âge / French summary of age estimation procedures. https://archimer.ifremer.fr/doc/00000/7294/ Boëns, A., Grellier, P., Lebigre, Ch. and Petitgas, P. (2021). Determinants of growth and selective mortality in anchovy and sardine in the Bay of Biscay. Fisheries Research, 239, 105947. https://doi.org/10.1016/j.fishres.2021.105947 Boëns, A., Ernande, B., Petitgas, P. and Lebigre, Ch. (2023). Different mechanisms underpin the decline in growth of anchovies and sardines of the Bay of Biscay. Evolutionary Applications, 16: 1393–1411. https://doi.org/10.1111/eva.13564  

This visualization product displays the total abundance of marine macro-litter (> 2.5cm) per beach, per 100m & to 1 survey aggregated over the period 2001 to 2020 from Marine Strategy Framework Directive (MSFD) monitoring surveys. EMODnet Chemistry included the collection of marine litter in its 3rd phase. Since the beginning of 2018, data of beach litter have been gathered and processed in the EMODnet Chemistry Marine Litter Database (MLDB). The harmonization of all the data has been the most challenging task considering the heterogeneity of the data sources, sampling protocols and reference lists used on a European scale. Preliminary processing were necessary to harmonize all the data: - Exclusion of OSPAR 1000 protocol: in order to follow the approach of OSPAR that it is not including these data anymore in the monitoring; - Selection of MSFD surveys only (exclusion of other monitoring, cleaning and research operations); - Exclusion of beaches without coordinates; - Some categories & some litter types like organic litter, small fragments (paraffin and wax; items > 2.5cm) and pollutants have been removed. The list of selected items is attached to this metadata (total abundance list). This list was created using EU Marine Beach Litter Baselines and EU Threshold Value for Macro Litter on Coastlines from JRC (these two documents are attached to this metadata); - Normalization of survey lengths to 100m & 1 survey / year: in some cases, the survey length was not exactly 100m, so in order to be able to compare the abundance of litter from different beaches a normalization is applied using this formula: Number of items (normalized by 100 m) = Number of litter per items x (100 / survey length) Then, this normalized number of items is summed to obtain the total normalized number of litter for each survey. Finally, a median is calculated over the entire period among all these total numbers of litter per 100m calculated for each survey. Sometimes the survey length was null or equal to 0. Assuming that the MSFD protocol has been applied, the length has been set at 100m in these cases. The size of each circle on this map increases with the calculated median number of marine litter per beach, per 100m & to 1 survey. The median litter abundance values displayed in the legend correspond to the 50 and 99 percentiles and the maximum value. More information is available in the attached documents. Warning: - the absence of data on the map doesn't necessarily mean that they don't exist, but that no information has been entered in the Marine Litter Database for this area. - This map was created to give an idea of the distribution of beach litter between 2001 and 2021 in a synthetic manner. NOT ALL BEACHES MAY HAVE DATA FOR THE ENTIRE PERIOD, SO IT IS NOT POSSIBLE TO MAKE A COMPARISON BETWEEN BEACHES.

Metabarcoding data were produced based on samples gathered at Ifremer where the DNA was extracted; PCR libraries were built at Ifremer and Genseq; libraries were sequenced at Novogene. The data to download contain: 1/d emultiplexed raw data, 2/ metadata, and 3) Scripts to process data and taxonomically assign DNA sequences 4) Rmarkdown to analyze communities.

This product displays for Anthracene, median values of the last 6 available years that have been measured per matrix and are present in EMODnet regional contaminants aggregated datasets, v2022. The median values ranges are derived from the following percentiles: 0-25%, 25-75%, 75-90%, >90%. Only "good data" are used, namely data with Quality Flag=1, 2, 6, Q (SeaDataNet Quality Flag schema). For water, only surface values are used (0-15 m), for sediment and biota data at all depths are used.

This product displays for Mercury, positions with values counts that have been measured per matrix for each year and are present in EMODnet regional contaminants aggregated datasets, v2022. The product displays positions for every available year.

In European sea bass like in other animals, the tongue plays a fundamental role in the mechanics of food ingestion. It is composed from the surface in depth of mucosa, submucosa, musculature and fibro cartilaginous skeleton. The tunica mucosa exhibits a stratified epithelium interrupted by numerous teeth differently distributed that erupt more or less completely from the layers below. The European sea bass tongue is composed of canine-like teeth, surrounded by taste buds and numerous fungiform and conical papillae. The tongue beeing directly in contact with external environment, the success of the adaptation of fishes to different environments in the context of global change, depends oamong other on the modifications occurring on the tongue structures. The present study investigates the potential effect of ocean acidification on the lingual transcriptome.

A consistent dataset of bottom trawl survey data spanning 47 years in the Bay of Biscay was assembled. The dataset includes data from the current EVHOE survey from 1987 to 2019 and two previous surveys carried out in 1973 and 1976. The recent EVHOE time-series from 1997 is also available from DATRAS (https://www.ices.dk/data/data-portals/Pages/DATRAS.aspx). The catch in numbers and weight (kg) per haul of all Rajiformes species caught in these surveys is provided. Haul information is provided for all hauls, including those with no catch of Rajiformes. Areas of the sampling strata of the survey and spatial polygones of these strata are provided in separate files.

Species distribution models (GAM, Maxent and Random Forest ensemble) predicting the distribution of Acanella arbuscula assemblage in the Celtic Sea. This community is considered ecologically coherent according to the cluster analysis conducted by Parry et al. (2015) on image sample. Modelling its distribution complements existing work on their definition and offers a representation of the extent of the areas of the North East Atlantic where they can occur based on the best available knowledge. This work was performed at the University of Plymouth in 2021.

This benchmark dataset contains the physical data used as predictors to reconstruct global chlorophyll-a concentrations (Chl, a proxy of phytoplankton biomass) in Roussillon et al., as well as the reference satellite Chl target fields. The nine physical predictors' data (Short-Wave radiations, Sea Surface Temperature, Sea Level Anomaly, Zonal and meridional surface currents, Zonal and meridional surface wind stress, Bathymetry, Binary continental mask) were extracted from publicly available datasets over [1998-2015] and resampled to the same spatio-temporel resolution as Chl, i.e. monthly on a 1°x1° grid between 50°N and 50°S. Missing values were gap-filled using the heat diffusion equation. Each variable was normalized by substracting its mean from the original values and dividing by its standard deviation over [1998-2015]. This dataset was used to train and validate the Multi-Mode Convolutional Neural network (CNNMM8) introduced in Roussillon et al. ; reconstructed monthly Chl fields over the [2012-2015] test period are also provided here. We hope this benchmark dataset can help to promote the improvements of methods as well as the emergence of new ideas, as building datasets is sometimes more time-consuming than the implementation of machine learning tools themselves. This would also facilitate the quantitative comparison of models performances' on the exact same datasets.

This product displays for Benzo(a)pyrene, median values of the last 6 available years that have been measured per matrix and are present in EMODnet regional contaminants aggregated datasets, v2022. The median values ranges are derived from the following percentiles: 0-25%, 25-75%, 75-90%, >90%. Only "good data" are used, namely data with Quality Flag=1, 2, 6, Q (SeaDataNet Quality Flag schema). For water, only surface values are used (0-15 m), for sediment and biota data at all depths are used.