1) Demographic traits These data are published data of age-specific mortality rates, age-specific lengths or weights, length and age at maturity, fecundity-length relationships, and egg size for 84 populations from 49 species of primarily commercial teleost fishes. The populations included are those for which all the life history traits under study have been estimated over a period shorter than 10 years. Traits were estimated from within the ten year window or averaged across it when data were available. Only studies in which reference population, sample size, techniques used for ageing fish and counting eggs, and models used for estimating mortality were reported are included. When only a size or age range was available, the midpoint between the extreme values was used. Raw data were converted into seven demographic traits: - Time-to-5%-survival (T.05): the time elapsed from sexual maturity until 95% of a cohort is dead. T.05 fwas estimated from an exponential mortality model, based on total mortality coefficients estimated by Virtual Population Analysis (age-structured model) in most cases or cohort analysis or catch curves. - Length-at-5%-survival (L.05). In fishes, adult size is difficult to measure because of their indeterminate growth. Adult size reported here is length at time-to-5%-survival. - Age at sexual maturity (Tm): median age at maturity was estimated directly from the data or by fitting a logistic curve to age-specific proportion mature data. When only an age range was available, the midpoint between minimum and maximum is reported. - Length at sexual maturity (Lm): median length at maturity was estimated as age at maturity. - Slope of the fecundity-length relationship (Fb): fish fecundity, defined as the number of eggs present in the ovaries immediately before spawning, is known to increase intraspecifically with the size of females. This increase is usually described by a power-law F = aLb. The exponent of this relationship, b (slope of the log-log fecundity-length regression), accounts for the increase in fecundity with size. - Fecundity at maturity (Fm): fecundity in the year of maturity was estimated from length at maturity, the fecundity-length relationship and the number of spawning bouts per year for batch spawners. - Egg volume (Egg): When information on egg size was unavailable in specific papers, values were borrowed from other studies, using the following criteria in the descending order: from the same period, the same population, the same species. In five species of Perciformes no estimate was available for any population, thus egg volume was estimated from other species of the same family. 2) Fishing pressure Three types of environments with low, moderate and high fishing pressure were defined. - To scale the pressure exerted by fishing to the natural population turn-over, it was expressed as the ratio of fishing mortality to natural mortality rates (F/M). Data were gathered from the literature together with demographic traits. Authors use the following methods to estimate natural mortality rates: intercept of a regression of total mortality on fishing effort, linear relationship known between estimates of natural mortality, growth parameters and the temperature, or multispecies models. Fishing mortality rates were estimated from Virtual Population Analysis or cohort analysis, or as the difference between total and natural mortality. Three levels of fishing pressure were defined: low fishing pressure (fishing mortality lower than natural mortality, F/M < 1), intermediate (1 <= F/M < 2) and high (F/M >= 2).

The data come from organisms and pictures collected during the MEDITS annual bottom trawl surveys conducted between 2011 and 2013 (Bertrand et al. 2002). MEDITS surveys cover the continental shelf (10 m to 200 m depth) and the upper part of the continental slope (200 m to 800 m) on the Mediterranean. A total of 1511 individuals from 85 fish species were collected from seven Mediterranean areas (South Adriatic Sea, Sardinia, Gulf of Lions, around Cyprus, Mallorca, Tyrrhenian Sea, and North West Ionian Sea). A set of 14 morphological traits related to the habitat and the diet of the species were measured in the field and on pictures using the ImageJ software (version 1.47, http://imagej.nih.gov/ij/) (see Granger et al. 2015 and Brind'Amour et al. submitted for details) (Figure 1). Replicats of measures vary between 1 (e.g. Scorpaena loppei) to 53 (e.g. Serranus hepatus) according to fish species. Twelve of the chosen traits consist in continuous biological characteristics measured on each individual (measured in cm). The two remaining traits are categorical and determined at the species level.

Data were collected from the regional program LOUPE (Observation of the habitat and associated communities in the context of the fisheries of the Capbreton Canyon). It consisted in the observations of two métiers practiced around the canyon. The observations were carried out between July 2011 and April 2013 on coastal boats. Observations and interviews were made on board commercial vessels. The longlines used in the hake fishery are semi-pelagic and are deployed on the edge of the Capbreton Canyon. It is an emblematic and major métier benefiting from a particular regulation as they take advantage of a prohibition of net and trawl fishing on their fishing grounds. Between 8 and 14 costal boats practice this métier during the year and the fleet characteristics are homogeneous. Boats lay between 1,200 and 1,800 hooks per day, baited with frozen pilchard (Sardina pilchardus). Two or three men are on board these vessels. Fishing is mostly practiced in spring and summer but a small number of vessels work all year. Generally, trips last between ten and twelve hours; longline is set before sunrise and retrieved three or four hours later. Hake is the main targeted species; other targets are pollack (Pollachius pollachius), red sea bream (Pagellus bogaraveo) and conger (Conger conger). Netting is a major métier in terms of vessels involved and the number of trips. Crew composition varies and depends on boat length (from one to four men on average). This métier is practiced by 30 to 35 boats all year round, but fleet characteristics are less homogeneous than in the case of longliners . The strategy of these netters operating in the coastal area is based on the use of several types of nets (gillnets and trammel nets) targeting several species, often sold directly to consumers on the docks. Gillnets, consisting of a single mesh, target hake, sea bass and sea bream species (Diplodus spp, Sparus aurata, Litognathus mormyrus), while the trammel nets (three meshes) are used to capture benthic fish, such as common sole, monkfish (Lophius spp), turbot and brill (Scophthalmus rhombus). Generally, trips last less than twelve hours for coastal netters (less than 15 m), which predominate in the sector, and a few days for large netters. On average, the coastal vessels set 6000 to 8000 m. nets daily.

In 2003 two experiments were carried out in the Bay of Biscay to compare catch numbers obtained in standard research 30-min hauls with those from 0-min hauls to determine the so called end effect. The end effect in trawl catches is defined as the proportion of the fish catch taken during shooting and hauling of the net, a period excluded from what is nominally referred to as haul duration. In 0-hauls the trawl was hauled as soon as the trawl geometry stabilized on the seabed. The trawl used was a beam trawl rigged as twin trawl. Overall 24 hauls were carried out, six 30-min and 18 0-min hauls. Average catch ratios (0-min/30-min hauls) ranged from 0.05 (s.d. 0.06) for sole to 0.34 (s.d. 0.64) for hake.

This dataset comprises stomach contents from 2004 to 2022 for the five dominant small pelagic fish species, anchovy (Engraulis encrasicolus), sardine (Sardina pilchardus), mackerel (Scomber scombrus), sprat (Sprattus, sprattus) and horse mackerel (Trachurus trachurus) on the french shelf of the Bay of Bisacy in spring. The dataset represents a unique long-term monitoring of stomach contents characterized with a low taxonomic resolution and semi-quantitative abundance quotation. The data were acquired on the PELGAS survey series. This integrated survey is run in each year in May since 2000, to monitor the Bay of Biscay pelagic ecosystem at springtime and assess the biomass of its small pelagic fish species. Survey protocols are detailed in Doray et al. 2018. During the survey, pelagic trawl hauls are undertaken to identify echotraces to species and to measure individual fish traits. All hauls are performed during day time. The fish stomachs were sampled from the haul catch. For a given species, twenty individuals were selected at random from the catch, their stomachs dissected and preserved. This was repeated at three hauls in each of the ten spatial strata defined to cover the entire Biscay shelf. Stomach sampling by species depended on the trawl haul catch and all species were not systematically sampled jointly at the same trawl haul. Also, stomach sampling intensity varied between species and years. The stomachs were preserved in formaline until 2018 and in ethanol since. The taxonomic analysis of stomach contents was performed in the laboratory under a binocular magnifyer by the company LAPHY. A simplified taxonomic resolution was used, which considered five icthtyoplankton groups, two copepod groups, euphausids or mysids, amphipods, two decapod groups, other crustacea, other zooplankton, phytoplankton and pulp. Taxon abundance was defined by a quotation : 0 (absence), 1 (presence : <10 individuals), 2 (abundant : between 10 and 100), 3 (very abundant : > 100). The dataset comprises trawl haul information, information on the quality of the stomach contents and abundance quotes for the list of plankton taxons.

The Pélagiques Gascogne (PELGAS, Doray et al., 2000) integrated survey aims at assessing the biomass of small pelagic fish and monitoring and studying the dynamics and diversity of the Bay of Biscay pelagic ecosystem in springtime. PELGAS has been conducted within the EU Common Fisheries Policy Data Collection Framework and Ifremer’s Fisheries Information System. The PELGAS survey model has allowed for the establishment of a long-term time-series of spatially-explicit data of the Bay of Biscay pelagic ecosystem since the year 2000. Main sampled components of the targeted ecosystem are: hydrology, phytoplankton, mesozooplankton, fish and megafauna (cetacean and seabirds). This dataset presents gridded maps of standard pelagic ecosystem parameters collected in the main sampled components during the PELGAS survey. Ecosystem parameters were mapped on a 15km x 15km grid by applying a block averaging procedure (Petitgas et al., 2009, 2014). The dataset also includes the ecologically meaningful survey dates proposed by Huret et al. (2017), mapped on the same grid. Details on survey protocols and data processing methodologies can be found in Doray et al., (2014, 2017a). This dataset was used in Authier et al., 2017; Doray et al., 2017b, 2017c, 2017a; Huret et al., 2017; Petitgas et al., 2017.

The anchovy (Engraulis encrasicolus) and sardine (Sardina pilchardus) populations in the Bay of Biscay are jointly surveyed each year in May since 2000 and in September since 2003 by means of acoustic surveys. The integrated survey PELGAS (Doray et al., 2018) is run in May by France and covers the French shelf of the Bay of Biscay. Its objectives are to monitor the Bay of Biscay pelagic ecosystem in springtime and assess the biomass of its small pelagic fish species, including sardine and anchovy. Amongst many information on the ecosystem, the survey PELGAS provides knowledge on the adults of anchovy and sardine during their spawning in spring. The survey JUVENA (Boyra et al., 2013) is run in September by Spain. It has a larger spatial coverage than PELGAS, including part of the Spanish coast and open ocean outside the shelf because it targets juvenile anchovy. It also provides knowledge on sardine as well as other pelagic species. Both surveys are coordinated by the ICES Working Group on Acoustic and Egg Surveys for Small Pelagic Fish (WGACEGG), together with other pelagic surveys in ICES areas 7, 8 and 9. Survey protocoles are detailed in Doray et al. (2021). Briefly, fish backscatter data are recorded along the survey transect lines and pelagic trawl hauls are undertaken opportunistically to identify the echotraces to species and collect fish samples for biometric data. The trawl haul catches have provided the anchovy and sardine length data, from which the maps presented here are derived. At each trawl haul, the catch is sorted by species and weighted. A subsample by species is measured to estimate the species’ length distribution. The four maps presented here correspond to the average maps of anchovy and sardine length distributions in May and September, derived from the PELGAS and JUVENA trawl haul data series. The maps were obtained by kriging, following the procedure explained in Petitgas et al. (2011) for mapping functions instead of variables. For each species, the experimental length distribution at each haul was fitted by a linear combination of Legendre polynomials, the coefficients of which were co-kriged. The number of polynomials varied from 15 to 22 depending on the survey and species, with a higher number for sardine and in autumn. The length histogram at each grid node was then deduced from the mapped coefficients. When the length distribution at a given haul was estimated with less than 40 individual fish, the haul was not taken into account for mapping. This threshold defined presence and absence of the species in the haul data sets. The trawl hauls from 2000 to 2019 were pooled for the PELGAS series (1965 stations) and from 2003 to 2020 for JUVENA (852 stations). The mapping was performed on the same grid for both PELGAS and JUVENA and both species, and with similar moving kriging neighbourhoods. The grid has a mesh size of 0.25 x 0.25 decimal degree square. In addition to mapping the length distribution, presence/absence was mapped for each species by ordinary kriging on the same grid and with the same neighbourhoods as previously. The computations were performed in R (version 4.0.5) with the RGeostats package (version 13.0.1) freely available at http://rgeostats.free.fr. The map data files comprise for each species the following information: the geographical coordinates of the grid points, the probability of presence and the probability of each length class of width 0.5 cm ranging from 2.5 to 27 cm.

Input data, TMB (C++) and R code for close-kin mark recapture (CKMR) abundance estimation for two subpopulations of thornback ray (Raja clavata) in the central Bay of Biscay (offshore and Gironde estuary, see figure). Samples were taken between 2015 to 2020. Parent-offspring pairs were identified using SNP genotype information. Birth years of individuals were estimated using length information and growth curves by sex.

The Pélagiques Gascogne (PELGAS, Doray et al., 2000) integrated survey aims at assessing the biomass of small pelagic fish and monitoring and studying the dynamics and diversity of the Bay of Biscay pelagic ecosystem in springtime. PELGAS has been conducted within the EU Common Fisheries Policy Data Collection Framework and Ifremer’s Fisheries Information System. Details on survey protocols and data processing methodologies can be found in Doray et al., (2014, 2018). This dataset comprises the abundance (no. of individuals), biomass (metric tons), mean length (cm), mean weight (g) of marine organisms collected by midwater trawling to identify fish echoes detected during PELGAS surveys (2000-2018). All parameters have been raised to the trawl haul level. Trawl haul metadata and species reference list are also provided.

In 1967, E.Postel, researcher at the OSTPM (Scientific and Technical Office for Maritime Fisheries) set up a data collection system on albacore catches by French fleets. JC Dao and FX Bard continued this work within CNEXO (National Center for the Exploitation of Oceans) and then at IFREMER from 1984. This information was transmitted by fishing professionals via logbooks, on the basis of volunteering (Dao, 1971, Bard, 1977). In 1982, the European Community put in place a mandatory system of declarations of fishing effort and catches via logbooks (EC Regulation No. 2057 in Sanchez and Santurtun, 2013). As a result, the two systems persisted between 1982 and 1986, with European logbooks gradually supplanting logbooks