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The ICES Working Group on Fisheries Benthic Impact and Trade-offs (WGFBIT) has developed an assessment framework based on the life history trait longevity, to evaluate the benthic impact of fisheries at the regional scale. In order to apply this framework to the Mediterranean sea, several Mediterranean longevity databases were merged together with existing North-East Atlantic ones to develop a common database. Longevity was fuzzy coded into four longevity classes: <1, 1-3, 3-10 and >10 years. Both benthic mega and macrofauna organisms are included in this dataset. Further details about both the purpose and the methodology may be found in ICES (2022) and Cuyvers et al. (2023). The result of the final dataset merging is one dataset containing the fuzzy coded average longevity (and standard deviation) for 2264 taxa and for each, the number of databases used.
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The Arcachon Bay is a unique and ecologically important meso-tidal lagoon on the Atlantic coast of south-west France. The Arcachon Bay has the largest area of dwarf seagrass (Z. noltei) in Europe, the extent of which was stable in their extent between the 1950s and 1990s, but a decline in seagrass was observed in mid-2000. The decline of Zostera (seagrass) may have a significant impact on sedimentation in this coastal ecosystem rich in marine life. Interface cores were collected in September 2022 to determine sediment and mass accumulation rates (SAR, MAR) in the Arcachon Bay. Ten study areas were selected, distributed over most of the areas where seagrass meadows are actually observed. Two sites were visited each time, one with the presence of Zostera noltei in good condition (Healthy) and the other where the sediment was bare (Bare). Maximum water heights during spring tides range from 3.44 m for the deepest site (Garrèche) to 2.09 m for the shallowest site (Fontaines). A total of 20 sediment cores were sampled and carefully extruded every 1 cm from the top to the bottom of the core. The sediment layers were used to determine dry bulk density and selected radioisotope activities: DBD, 210Pb, 226Ra, 137Cs, 228Th and 40K expressed as %K).
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The willingness to pay (WTP) of people to protect animal populations can be used as a tool for these populations’ conservation. The WTP reflects the non-use value of animals, which can be significant for charismatic species. This value can be used as an economic criterion for decision-makers in order to recommend protective measures. The definition of the WTP to protect a species is challenging, as valuation methods are time-consuming and expensive. To overcome these limitations, we built a benefit transfer function based on 112 valuation studies and apply it to 440 Mediterranean marine species. We extracted these species from the IUCN database and retrieved some required parameters from, amongst others, the FishBase database. Marine mammals appear to have the highest WTP value followed in order by sea turtles, sharks and rays, and ray-finned fishes. Commercial fish species appear to have the highest values amongst the fish class.
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Mesoscale dynamics in the Mediterranean Sea have been investigated for years and anticyclonic eddies are regularly observed features in the Algerian Basin. In early spring 2016, a field experiment during the ProtevsMed 2016 cruise thoroughly investigated this specific eddy, when it was located near the North Balearic Front, taking high-resolution (Seasoar) hydrological transects, several CTD casts and LADCP measurements. In addition, four drifting buoys were released in the eddy core. These in situ measurements revealed that the vertical structure of this anticyclone was made of two water lenses of very different origins (Atlantic Water above and Western Intermediate Water below) spinning together. In the vicinity of the North Balearic Front, which may act as a dynamical barrier for structures, the eddy interacted with a subsurface anticyclonic eddy made of modal water, which fostered cross-front exchanges generating filaments by stirring. The high-resolution sampling revealed fine scales structures both adjacent to the eddy and within its core. The eddy has been targeted from 21 March to 1 April 2016 taking advantage of a meteorological window. It has been sampled with: - a towed undulating vehicle, the SeaSoar designed and built by Chelsea Instruments; it gets mounted on its sides two Sea-bird SBE-9 (SBE 3 temperature and SBE 4 conductivity sensors) and a Wetlabs Fluorometer of type ChloroA WetStar - CTD casts performed with a Sea-bird SBE-9 (SBE 3 temperature and SBE 4 conductivity sensor) and an RDI 150 kHz current profiler mounted in a general oceanics 12-place rosette, with12l Niskin bottles - drifters with holey-sock positioned at 50 m deep below the expected Ekman layer thickness (remaining in the eddy until mid May).
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The dataset includes age- and length-based catch per unit effort data for commercial fish species collected by the French trawl survey EVHOE.
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The West Gironde Mud Patch (WGMP) is a mud deposit located 25 km from the mouth of the Gironde Estuary in the Bay of Biscay. This 4-metre-thick clay-silt feature, which extends over an area of 420 km2, is found at depths between 30 and 80 meters. The main objectives of the JERICObent7 cruise, in July 2019, were to characterise the evolution of the WGMP’s benthic ecosystem in terms of its sedimentary, biogeochemical and ecological properties and to reconstruct climate variations and identify potential anthropogenic impacts over the last few centuries. To this end, a precise chronological framework was established for the sedimentary archives of the last few decades using 210Pbxs (T1/2 = 22.3 years). Interface cores were collected at stations 1, 3 and 4 along a cross-shelf transect. Twin Kullenberg cores were collected at sites 3 and 4 for geochemical (KGL) and palaeoceanographic (JB7-ST) investigations. Each interface core was carefully extruded at 0.5 cm intervals from the top of the core to 4 cm, and then at 1 cm intervals until the bottom was reached. Kullenberg cores were only collected at sites 3 and 4. Depending on their intended use, the Kullenberg cores were sampled at different resolutions, the depth of each sediment layer corresponded to the depth from the top of the core. These layers were then used to determine the dry bulk density and radioisotope activities of interest (210Pb, 226Ra, 228Th, 137Cs, 40K). Excess 210Pb was used to establish the realignment and chronological framework of the interface and Kullenberg cores.
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210Pb, 226Ra and 137Cs were measured by non-destructive gamma spectrometry on marine sediment cores, collected during RIKEAU 2002 cruise on board r/v Thalia, on the shelf of the Bay of Biscay
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In October 2019 we chose 15 sites from the 2019 EVHOE survey for environmental DNA (eDNA) sampling. The French international EVHOE bottom trawl survey is carried out annually during autumn in the BoB to monitor demersal fish resources. At each site, we sampled seawater using Niskin bottles deployed with a circular rosette. There were nine bottles on the rosette, each of them able to hold ∼5 l of water. At each site, we first cleaned the circular rosette and bottles with freshwater, then lowered the rosette (with bottles open) to 5 m above the sea bottom, and finally closed the bottles remotely from the boat. The 45 l of sampled water was transferred to four disposable and sterilized plastic bags of 11.25 l each to perform the filtration on-board in a laboratory dedicated to the processing of eDNA samples. To speed up the filtration process, we used two identical filtration devices, each composed of an Athena® peristaltic pump (Proactive Environmental Products LLC, Bradenton, Florida, USA; nominal flow of 1.0 l min–1 ), a VigiDNA 0.20 μm filtration capsule (SPYGEN, le Bourget du Lac, France), and disposable sterile tubing. Each filtration device filtered the water contained in two plastic bags (22.5 l), which represent two replicates per sampling site. We followed a rigorous protocol to avoid contamination during fieldwork, using disposable gloves and single-use filtration equipment and plastic bags to process each water sample. At the end of each filtration, we emptied the water inside the capsule that we replaced by 80 ml of CL1 conservation buffer and stored the samples at room temperature following the specifications of the manufacturer (SPYGEN, Le Bourget du Lac, France). We processed the eDNA capsules at SPYGEN, following the protocol proposed by Polanco-Fernández et al., (2020). Half of the extracted DNA was processed by Sinsoma using newly developped ddPCR assays for European seabass (Dicentrachus labrax), European hake (Merluccius merluccius) and blackspot seabream (Pagellus bogaraveo). The other half of the extracted DNA was analysed using metabarcoding with teleo primer. The raw metabarcoding data set is available at https://www.doi.org/10.16904/envidat.442 Bottom trawling using a GOV trawl was carried out before or after water sampling. The catch was sorted by species and catches in numbers and weight were recorded. No blackspot seabream individuals were caught. Data content: * ddPCR/: contains the ddPCR counts and DNA concentrations for each sample and species. * SampleInfo/: contains the filter volume for each eDNA sample. * StationInfo/: contains metadata related to the data collected in the field for each filter. * Metabarcoding/: contains metabarcoding results for teleoprimer. * Trawldata/: contains catch data in numbers and weight (kg).
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Opportunistic macroalgae blooms (green tides) data are collected during monitoring surveys on the English Channel / Bay of Biscay French coasts since 2008 (Quadrige program code : BLOOMS). Protocols are implemented in the European Water Framework Directive.
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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.
Catalogue PIGMA