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This dataset contains bio-optical measurements from BioGeoChemical-Argo (BGC-Argo) profiling floats complemented with ocean-colour satellite matchups of variables related to the detection of coccolithophore blooms dominated by Emiliania huxleyi. BGC-Argo float data cover the global ocean from November 2012 to December 2018 and include measurements of the particulate backscattering coefficient (BBP_float in m-1), the concentration of Chlorophyll-a (CHLA_float in mg m-3), and the particulate beam attenuation coefficient (CP_float in m-1) with data processing and quality control described in the manuscript entitled “Detection of coccolithophore blooms with BioGeoChemical-Argo floats” submitted to Geophysical Research Letters. The data represent near-surface ocean conditions, calculated as the average value in the top 15m of the water column. Daily ocean-colour satellite data were downloaded from the GlobColour project (ftp://ftp.hermes.acri.fr) with a spatial resolution of 4km and matched with every BGC-Argo float observation by using a 5x5 pixel box and a 9-day temporal window. For each float observation, we extracted concurrent satellite data of the concentrations of Particulate Inorganic Carbon (PIC_sat in mmol m-3) and Particulate Organic Carbon (POC_sat in mmol m-3), from which we derived the proportion of PIC_sat to the total particulate carbon concentration (PIC_POC_sat in % and defined as PIC_sat / [PIC_sat+POC_sat]). Coccolithophore bloom periods were identified using annual times series of PIC_sat and PIC_POC_sat at each profile location as described in the submitted manuscript, and the column “inside_coccolithophore_bloom” reports the float observations occurring inside such blooms.
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Understanding the dynamics of species interactions for food (prey-predator, competition for resources) and the functioning of trophic networks (dependence on trophic pathways, food chain flows, etc.) has become a thriving ecological research field in recent decades. This empirical knowledge is then used to develop population and ecosystem modelling approaches to support ecosystem-based management. The TrophicCS data set offers spatialized trophic information on a large spatial scale (the entire Celtic Sea continental shelf and upper slope) for a wide range of species. It combines ingested prey (gut content analysis) and a more integrated indicator of food sources (stable isotope analysis). A total of 1337 samples of large epifaunal invertebrates (bivalve mollusks and decapod crustaceans), zooplankton, fish and cephalopods, corresponding to 114 species, were collected and analyzed for stable isotope analysis of their carbon and nitrogen content. Sample size varied between taxa (from 1 to 52), with an average of 11.72 individuals sampled per species, and water depths ranged from 57 to 516 m. The gut contents of 1026 fish belonging to ten commercially important species: black anglerfish (Lophius budegassa), white anglerfish (Lophius piscatorius), blue whiting (Micromesistius poutassou), cod (Gadus morhua), haddock (Melanogrammus aeglefinus), hake (Merluccius merluccius), megrim (Lepidorhombus whiffiagonis), plaice (Pleuronectes platessa), sole (Solea solea) and whiting (Merlangius merlangus) were analyzed. The stomach content data set contains the occurrence of prey in stomach, identified to the lowest taxonomic level possible. To consider potential ontogenetic diet changes, a large size range was sampled. The TrophicCS data set was used to improve understanding of trophic relationships and ecosystem functioning in the Celtic Sea. When you use the data in your publication, we request that you cite this data paper. If you use the present data set (TrophicCS) for the majority of the data analyzed in your study, you may wish to consider inviting at least one author of the core team of this data paper to become a collaborator /coauthor of your paper.
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EVHOE (« Evaluation Halieutique de l’Ouest Européen ») surveys provide observational data on bentho-demersal communities on the continental shelves of the Bay of Biscay and the Celtic Sea for more than 30 years. The surveys operate a standardized bottom trawling gear and are conducted from 15 to 600 m depth, usually in the fourth quarter of the year, starting at the end of October. The main objectives are the monitoring of 22 commercial stocks of fish species and 10 cephalopods from the North-East Atlantic. The dataset also provide a description of regional diversity, including 250 taxa of fish, 45 taxa of cephalopods and others “commercial” invertebrates and, from 2008, more than 350 other taxa of benthic invertebrates. The acquisition of this dataset, organised by IFREMER, is steered by the IBTS working group organised within the framework of ICES. It is being funded by the European DCMAP programme, in coordination with the French Directorate-General for Maritime Affairs, Fisheries and Aquaculture (DGAMPA). This dataset is of great interest for the long-term monitoring of the continental shelves of the Bay of Biscay and the Celtic Sea. Moreover, on a larger scale, by being integrated into a European network of bottom trawl surveys, these data play an essential role in studying the evolution of ecosystems from continental shelves to the scale of the eastern North Atlantic. From April 2025, the proposed data have been updated in the latest standard format recognised by IFREMER (‘ELFIC’ format). The 5 data tables are compiled in a .zip file which also contains a document detailing the content of each table and their respective data fields.
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As part of the marine water quality monitoring of the “Pertuis” and the “baie de l’Aiguillon” (France), commissioned by the OFB and carried out by setec énergie environnement, three monitoring stations were installed. Two of them were set up at the mouths of the Charente and Seudre rivers on February 6 and 27, 2019, respectively, while a third was deployed in the Bay of Aiguillon on March 24, 2021. The dataset presented here concerns the station installed in the Charente estuary. Measurements are organized into .csv files, with one file per year. Data is collected using a SAMBAT multiparameter probe, which records the following parameters: - Temperature (-5 to 35 °C) - Conductivity (0 to 10 mS/cm) - Pressure (0 to 10 m) - Turbidity (0 to 300 NTU) - Dissolved Oxygen (0 to 20 mg/L & 0 to 200 %) - Fluorescence (0 to 50 µg/l) - PH (0/14)
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LOCEAN has been in charge of analyzing the isotopic composition of the dissolved inorganic carbon (DIC) in sea water collected during a series of cruises or ships of opportunity mostly in the southern Indian Ocean , the North Atlantic, and the equatorial Atlantic, but also in the Mediterranean Sea and in the equatorial Pacific. The LOCEAN sea-water samples for δ13CDIC were collected in 125/25 ml glass bottles until 2022/since then and poisoned with HgCl2 (1 ml of saturated solution) before storage in a dark room à 4°C until their measurement. The DIC was extracted from the seawater by acidification with phosphoric acid (H3PO4 85%) and CO2 gas that was produced was collected in a vacuum system following the procedure described by Kroopnick (1974). The isotopic composition of CO2 was determined using a dual inlet-isotopic ratio mass spectrometer (SIRA9-VG) by comparing the 13C/12C ratio of the sample to the 13C/12C ratio of a reference material, the Vienna-Pee Dee Belemnite (V-PDB). The isotopic composition is expressed in the δ-unit defined by Craig (1957)(method type 2). Experience showed that samples older than 3-4 years are likely to have experienced conservation issues and have been dismissed. The mass spectrometer has worked very well until 2014-2015. Afterwards, its aging as well as the aging of the preparation line resulted in more data loss, and often less accurate results. The preparation line was renovated in 2019, and analyses in 2020 were run manually, often repeating the measurement a second time for each sample. Up to 2007-2008, δ13CDIC values have a precision of±0.01 ‰ (Vangriesheim et al.,2009) and a reproducibility of±0.02 ‰. After an interlaboratory comparison exercise led by Claire Normandeau (Dalhousie University), results suggest that recent LOCEAN samples have a slightly poorer reproducibility (±0.04 ‰ ) as well as an offset of -0.13‰ (details available in Reverdin et al., ESSD 2018) that is confirmed by Becker et al. 2016 work by comparison with other cruises after removing the anthropogenic signal. Recent comparisons in early May 2021 with Orsay GEOPS facility samples suggest that the current offset is much smaller and might be +0.03‰. LOCEAN has installed in 2021 a new measurement device by coupling a Picarro G2131-I cavity ring down spectrometer (CRDS) with a CO2 extractor (Apollo SciTech) that will measure at the same time DIC (method type 3) (Leseurre, 2022). Since then, all water samples have been analyzed on this device. Part of the data set, as well as a scientific context and publications are also presented on the WEB site https://www.locean-ipsl.upmc.fr/oceans13c. Individual files correspond to regional subsets of the whole dataset. The file names are based on two letters for the region followed by (-) the cruise or project name (see below) followed by –DICisotopes, followed by either -s (surface data) or -b (subsurface data), and a version number (-V0, …): example SI-OISO-DICisotopes-s-V0; the highest version number corresponds to the latest update of the cruise/project data set, and can be directly downloaded. Earlier versions can be obtained on request, but are not recommended. The region two letters are the followings: - SI: station and surface data in the Southern Indian Ocean that include cruises : INDIGO I (1985 – stn) (https://doi.org/10.17600/85000111) CIVA I (1993 – stn & surf) (https://doi.org/10.17600/93000870) (Archambeau et al., JMS 1998) ANTARES (1993 – stn & surf) (https://doi.org/10.17600/93000600) OISO (*) (since 1998 – stn & surf) (https://doi.org/10.18142/228) (Racapé et al., Tellus 2010, Leseurre, 2022) - EA: station and surface data in the Tropical Atlantic Ocean that include cruises : EQUALANT (1999 & 2000 – surf) (https://doi.org/10.18142/98) EGEE (2005 to 2007 – stn & surf) (https://doi.org/10.18142/95) PIRATA (since 2013 – stn & surf) (https://doi.org/10.18142/14) EUMELI 2 (1991 – stn) (https://doi.org/10.17600/91004011) (Pierre et al., JMS 1994) BIOZAIRE 3 (2003 – stn & surf ) (https://doi.org/10.17600/3010120) (Vangriesheim et al., DSRII, 2009) TARA-Microbiomes (2021 - stn & surf) - NA : station and surface data in the North Atlantic Subpolar gyre that include cruises : OVIDE (**) (since 2002 – stn & surf) (https://doi.org/10.17882/46448) (Racapé et al., 2013) RREX (2017 – stn & surf) (https://doi.org/10.17600/17001400) SURATLANT (since 2010 - surf) (https://doi.org/10.17882/54517) (Racapé et al., BG 2014 ; Reverdin et al., ESSD 2018, Leseurre, 2022) NUKATUKUMA (since 2017- surf) - MS: station data in the Mediterranean sea that include cruises : ALMOFRONT 1 (1991 – stn) (https://doi.org/10.17600/91004211) VICOMED 3 (1990 – stn) (https://doi.org/10.17600/90000711) - PO: tropical Pacific that include cruises : PANDORA (2012 – stn) (https://doi.org/10.17600/12010050) ALIZE2 (1991 – stn & surf) (https://doi.org/10.17600/91002711) (Laube-Lenfant and Pierre, Oceanologica Acta 1994) - SO: station and surface data in the Southern Ocean (except OISO) that include cruises: TARA-Microbiomes (2021-2022, stn & surf) AGULHASII-072022 (2022, stn) CONFLUENCE (1993-1994, stn) - AO: station and surface data in the Arctic Ocean and nearby seas that include cruises: GREENFEEDBACK (2024, stn&surf) TCA (2024, stn) REFUGE ARCTIC (2024, stn) (*) The values for cruises OISO19, 21 and 22 are doubtful (for some, too low) and will require further investigation to find whether adjusted values can be proposed. (**) Some of the OVIDE cruises are also referred to as or GEOVIDE (in 2014), and BOCATS (in 2016). CATARINA, BOCATS1 and BOCATS2 (PID2019-104279GB-C21/AEI/10.13039/501100011033) cruises were funded by the Spanish Research Agency The values of the OVIDE 2010 stations are doubtful (too low), but no particular error was found, and they have been left in the files. Data The files are in csv format reported as: - Cruise name, station id, (bottle number), day, month, year, hour, minute, longitude, latitude, pressure (db), depth (m), temperature (°C), temperature qc, salinity (pss-78), salinity qc, d13CDIC, d13CDIC qc, method type - Temperature is an in situ temperature - Salinity is a practical salinity - Method type (1) acid CO2 extraction from helium stripping technique coupled to mass spectrometer, (2) acid CO2 extraction in a vacuum system coupled to mass spectrometer,(3) CO2 extractor (Apollo SciTech) coupled to CRDS measurements. Temperature qc, salinity qc, d13CDIC qc are quality indices equal to: - 0 no quality check (but presumably good data) - 1 probably good data - 2 good data - 3 probably bad data - 4 certainly bad data - 9 missing data (and the missing data are reported with an unlikely missing value)
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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.
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Long-term time series of coliform bacteria concentration (fecal coliform or Escherichia coli) in shellfish in four submarine areas (North Sea/Channel, Britany, Atlantic, Mediterranean).
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Understanding the spatial and temporal preferences of toxic phytoplankton species is of paramount importance in managing and predicting harmful events in aquatic ecosystems. In this study we address the realised niche of the species Alexandrium minutum, Pseudo-nitzschia fraudulenta and P. australis. We used them to highlight distribution patterns at different scales and determine possible drivers. To achieve this, we have developed original procedures coupling niche theory and habitat suitability modelling using abundance data in four consecutive steps: 1) Estimate the realised niche applying kernel functions. 2) Assess differences between the species’ niche as a whole and at the local level. 3) Develop habitat and temporal suitability models using niche overlap procedures. 4) Explore species temporal and spatial distributions to highlight possible drivers. Data used are species abundance and environmental variables collected over 27 years (1988-2014) and include 139 coastal water sampling sites along the French Atlantic coast. Results show that A. minutum and P. australis niches are very different, although both species have preference for warmer months. They both respond to decadal summer NAO but in the opposite way. P. fraudulenta realised niche lies in between the two other species niches. It also prefers warmer months but does not respond to decadal summer NAO. The Brittany peninsula is now classified as an area of prevalence for the three species. The methodology used here will allow to anticipate species distribution in the event of future environmental challenges resulting from climate change scenarios.
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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 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.
Catalogue PIGMA