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# Long-term changes in taxonomic and functional composition of European marine fish communities The GitHub linked repository is here: [European_demersal_fish_assemblages (](https://github.com/auroreRECE/European_demersal_fish_assemblages)DOI [10.5281/zenodo.11190119](https://zenodo.org/doi/10.5281/zenodo.11190119)) ## Overview This project is dedicated to studying the influence of environmental conditions and fishing on the functional and taxonomic structure of a demersal fish community in Europe. This GitHub repository provides the code of the Receveur et al. (2024) publication in Ecography. ## Data files description ### df\_MFA.csv This file contains the coordinates resulting from the Multiple Factor Analysis (MFA): * X : the row numbers ; * ID_unique : a unique ID number corresponding to the trawls ; * Dim.1 : the coordinate of each trawl on the first MFA dimension ; * Dim.2 : the coordinate of each trawl on the second MFA dimension ; * Dim.3 : the coordinate of each trawl on the third MFA dimension ; ### df\_PCA.csv This file contains the coordinates * X : the row numbers ; * ID_unique : a unique ID number corresponding to the trawls ; * Dim.1 : the coordinate of each trawl on the first PCA dimension ; * Dim.2 : the coordinate of each trawl on the second PCA dimension ; * Dim.3 : the coordinate of each trawl on the third PCA dimension ; ### df\_env.csv This file contains the following environmental parameters: * X : the row numbers ; * ID_unique : a unique ID number corresponding to the trawls ; * Year : the Year of each trawl ; * Quarter : the Quarter of each trawl ; * Ecoregion : the Ecoregion where each trawl has been done; * Survey : the name of the Survey ; * x_my_spatial_id : the longitude of the ICES rectangle where the trawl has been done ; * y_my_spatial_id : the latitude of the ICES rectangle where the trawl has been done ; * my_spatial_id : an ID for the ICES rectangle where the trawl has been done ; * depth : the bottom depth (meters) ; * depth_span : the bottom depth variability (maximum depth of the ICES cell - minimum depth) (meters) ; * chloro_mea: the mean chlorophyll-a concentration (mg/m³) ; * mlotst_mea : the mean mixed layer depth (meters) ; * oxy_bottom_mea : the mean bottom dissolved oxygen (umol/l) ; * oxy_surf_mea : the mean surface dissolved oxygen (umol/l) ; * temp_bottom_mea : the mean bottom temperature (°C) ; * temp_surf_mea : the mean surface temperature (°C) ; * curr_surf_mea : the mean surface current strength (m/s) ; * curr_bottom_mea : the mean bottom current strength (m/s) ; * sal_surf_mea : the mean surface salinity (PSU) ; * chloro_std : the standard deviation of chlorophyll-a concentration (mg/m³) ; * mlotst_std : the standard deviation of mixed layer depth (meters) ; * oxy_bottom_std : the standard deviation of bottom dissolved oxygen (umol/l) ; * oxy_surf_std : the standard deviation of surface dissolved oxygen (umol/l) ; * temp_bottom_std : the standard deviation of bottom temperature (°C) ; * temp_surf_std : the standard deviation of surface temperature (°C) ; * curr_surf_std : the standard deviation of surface current strength (m/s) ; * curr_bottom_std : the standard deviation of bottom current strength (m/s) ; * sal_surf_std : the standard deviation of surface salinity (PSU). ## Raw Data sources ### Biological data Trawls content is publicly available for the North East Atlantic (DATRAS database). Mediterranean data (MEDITS database) are available upon request to Maritime Affairs and Fisheries (MARE DATACOLLECTIONFRAMEWORK). The project uses the following surveys: | Survey Code | Survey name | Area | Period | References | | :---------- | :----------------------------------------------------- | :------------------------------------- | :-------: | :--------: | | BITS | Baltic International Trawl Survey | Baltic Sea | 1994-2019 | 4 | | BTS | Beam Trawl Survey | Celtic Sea; English Channel; North Sea | 1997-2019 | 7 | | BTS-VIII | Beam Trawl Survey – Bay of Biscay | Bay of Biscay | 2011-2019 | 7 | | DWS | Deepwater Survey | Irish Sea | 2006-2007 | 8 | | DYFS | Inshore Beam Trawl Survey | Southern North Sea | 2002-2019 | 7 | | EVHOE | French Southern Atlantic Bottom trawl Survey | Bay of Biscay and Celtic Sea | 2003-2019 | 1 | | FR-CGFS | French Channel ground Survey | English Channel | 1997-2019 | 2 | | IE-IAMS | Irish Anglerfish and megrim Survey | Scottish rockall and Irish Sea | 2016-2019 | 2 | | IE-IGFS | Irish Groundfish | Ireland Shelf Sea | 2003-2019 | 2 | | MEDITS | International bottom trawl survey in the Mediterranean | Mediterranean Sea | 1994-2018 | 9 | | NIGFS | Northern Ireland Groundfish Survey | Irish Sea | 2009-2019 | 2 | | NS-IBTS | North Sea International Bottom Trawl Survey | North Sea | 1997-2019 | 2 | | PT-IBTS | Portuguese International Bottom Trawl Survey | Portugal Shelf Sea | 2003-2017 | 2 | | ROCKALL | Scottish Rockall Survey (until 2010) | Rockall plateau | 2003-2009 | 2 | | SCOROC | Scottish Rockall Survey (from 2011) | Scottish plateau | 2011-2019 | 2 | | SCOWCGFS | Scottish West Coast Groundfish Survey | Scottish west coast | 2011-2019 | 2 | | SNS | Sole Net Survey | Southern North Sea | 2002-2019 | 7 | | SP-ARSA | Spanish Gulf of Cadiz Bottom Trawl Survey | Spain | 2003-2019 | 6 | | SP-NORTH | Spanish North Bottom Trawl Survey | North of Spain | 2003-2019 | 2 | | SP-PORC | Spanish Porcupine Bottom Trawl Survey | Irish Sea | 2003-2019 | 5 | | SWC-IBTS | Scottish West Coast International Bottom Trawl Survey | Scotland Shelf Sea | 1999-2010 | 2 | ### Trait data The complete traits data table is available upon request. It is a combination of the publicly available PANGAEA database, Fishbase information, and inference based on the FISHLIFE project. ### Environmental variables The data used are all publicly available on the Copernicus website. ### Fishing data The data used are all publicly available on the Global Fishing Watch website. ## Recommended Citation Please use the following citation: Receveur, A., Leprieur F., Ellingsen K., Keith D., Kleisner K., McLean M., Mérigot B., Mills K., Mouillot D., Rufino M., Trindade-Santos I., Van Hoey G., Albouy C., Auber A. Data for “Long-term changes in taxonomic and functional composition of European marine fish communities.” Dryad Digital Repository. (2024). doi.org/10.5061/dryad.x69p8czsj ## Acknowledgments This research is a product of the MAESTRO group funded by the synthesis center CESAB of the French Foundation for Research on Biodiversity (FRB). We thank France Filière Pêche (FFP) who founded the MAESTRO project. We also warmly thank all those who have contributed in any way to the scientific surveys and data collection/provision (European Institutions and scientists implicated in DATRAS-BTS, MEDITS, and DCF). ## References 1. ICES. The EVHOE survey (France). ICES Documents. (1997). Available at: https://archimer.ifremer.fr/doc/00036/14707/12013.pdf 2. ICES. Manual of the IBTS North Eastern Atlantic Surveys. Series of ICES Survey Protocols SISP 15 (2017). doi:10.17895/ices.pub.3519 3. ICES. Manual for the International Bottom Trawl Surveys Revision VIII. Series of ICES Survey Protocols SISP 10 - IBTS IX. (2015). 4. https://ices-library.figshare.com/articles/report/SISP_7_-*Manual_for_the_Baltic_International_Trawl_Surveys_BITS*/19050986 5. https://gis.ices.dk/geonetwork/srv/api/records/ce94a257-c8b3-44f7-9fd0-6bd7449ce073 6. http://ices.dk/sites/pub/CM%20Doccuments/2002/D/D0302A.pdf 7. https://ices-library.figshare.com/articles/report/SISP_14_-*Manual_for_the_Offshore_Beam_Trawl_Surveys_WGBEAM*/19051328 8. https://gis.ices.dk/geonetwork/srv/api/records/936b4fb7-9baa-4dbc-abd0-b1b7bda16406 9. https://archimer.ifremer.fr/doc/00117/22783/20585.pdf Evidence of large-scale biodiversity degradation in marine ecosystems has been reported worldwide, yet most research has focused on few species of interest or on limited spatiotemporal scales. Here we assessed the spatial and temporal changes in the taxonomic and functional composition of fish communities in European seas over the last 25 years (1994-2019). We then explored how these community changes were linked to environmental gradients and fishing pressure. We show that the spatial variation in fish species composition is more than two times higher than the temporal variation, with a marked spatial continuum in taxonomic composition and a more homogenous pattern in functional composition. The regions warming the fastest are experiencing an increasing dominance and total abundance of r-strategy fish species (lower age of maturity). Conversely, regions warming more slowly show an increasing dominance and total abundance of K-strategy species (high trophic level and late reproduction). Among the considered environmental variables, sea surface temperature, surface salinity, and chlorophyll-a most consistently influenced communities’ spatial patterns, while bottom temperature and oxygen had the most consistent influence on temporal patterns. Changes in communities’ functional composition were more closely related to environmental conditions than taxonomic changes. Our study demonstrates the importance of integrating community-level species traits across multi-decadal scales and across a large region to better capture and understand ecosystem-wide responses and provides a different lens on community dynamics that could be used to support sustainable fisheries management.

Project: GCOS Earth Heat Inventory - A study under the Global Climate Observing System (GCOS) concerted international effort to update the Earth heat inventory (EHI), and presents an updated international assessment of ocean warming estimates, and new and updated estimates of heat gain in the atmosphere, cryosphere and land over the period from 1960 to present. Summary: The file “GCOS_EHI_1960-2020_Earth_Heat_Inventory_Ocean_Heat_Content_data.nc” contains a consistent long-term Earth system heat inventory over the period 1960-2020. Human-induced atmospheric composition changes cause a radiative imbalance at the top-of-atmosphere which is driving global warming. Understanding the heat gain of the Earth system from this accumulated heat – and particularly how much and where the heat is distributed in the Earth system - is fundamental to understanding how this affects warming oceans, atmosphere and land, rising temperatures and sea level, and loss of grounded and floating ice, which are fundamental concerns for society. This dataset is based on a study under the Global Climate Observing System (GCOS) concerted international effort to update the Earth heat inventory published in von Schuckmann et al. (2020), and presents an updated international assessment of ocean warming estimates, and new and updated estimates of heat gain in the atmosphere, cryosphere and land over the period 1960-2020. The dataset also contains estimates for global ocean heat content over 1960-2020 for different depth layers, i.e., 0-300m, 0-700m, 700-2000m, 0-2000m, 2000-bottom, which are described in von Schuckmann et al. (2022). This version includes an update of heat storage of global ocean heat content, where one additional product (Li et al., 2022) had been included to the initial estimate. The Earth heat inventory had been updated accordingly, considering also the update for continental heat content (Cuesta-Valero et al., 2023).

Chronic, low intensity herbivory by invertebrates, termed background herbivory, has been understudied in tundra, yet its impacts are likely to increase in a warmer Arctic. The magnitude of these changes is however hard to predict as we know little about the drivers of current levels of invertebrate herbivory in tundra. We assessed the intensity of invertebrate herbivory on a common tundra plant, the dwarf birch (Betula glandulosa-nana complex), and investigated its relationship to latitude and climate across the tundra biome. Leaf damage by defoliating, mining and gall-forming invertebrates was measured in samples collected from 192 sites at 56 locations. Our results indicate that invertebrate herbivory is nearly ubiquitous across the tundra biome but occurs at low intensity. On average, invertebrates damaged 11.2% of the leaves and removed 1.4% of total leaf area. The damage was mainly caused by external leaf feeders, and most damaged leaves were only slightly affected (12% leaf area lost). Foliar damage was consistently positively correlated with mid-summer (July) temperature and, to a lesser extent, precipitation in the year of data collection, irrespective of latitude. Our models predict that, on average, foliar losses to invertebrates on dwarf birch are likely to increase by 6--7% over the current levels with a 1 textdegreeC increase in summer temperatures. Our results show that invertebrate herbivory on dwarf birch is small in magnitude but given its prevalence and dependence on climatic variables, background invertebrate herbivory should be included in predictions of climate change impacts on tundra ecosystems.

As Earth’s climate has varied strongly through geological time, studying the impacts of past climate change on biodiversity helps to understand the risks from future climate change. However, it remains unclear how paleoclimate shapes spatial variation in biodiversity. Here, we assessed the influence of Quaternary climate change on spatial dissimilarity in taxonomic, phylogenetic, and functional composition among neighboring 200-kilometer cells (beta-diversity) for angiosperm trees worldwide. We found that larger glacial-interglacial temperature change was strongly associated with lower spatial turnover (species replacements) and higher nestedness (richness changes) components of beta-diversity across all three biodiversity facets. Moreover, phylogenetic and functional turnover was lower and nestedness higher than random expectations based on taxonomic beta-diversity in regions that experienced large temperature change, reflecting phylogenetically and functionally selective processes in species replacement, extinction, and colonization during glacial-interglacial oscillations. Our results suggest that future human-driven climate change could cause local homogenization and reduction in taxonomic, phylogenetic, and functional diversity of angiosperm trees worldwide.

Acid–base disturbances caused by environmental factors and physiological events including feeding have been well documented in several fish species, but little is known about the impact of dietary electrolyte balance (dEB). In the present study, we investigated the effect of feeding diets differing in dEB ( − 100, 200, 500 or 800 mEq/kg diet) on the growth, nutrient digestibility and energy balance of Nile tilapia. After 5 weeks on the test diet, the growth of the fish was linearly affected by the dEB levels (P< 0·001), with the lowest growth being observed in the fish fed the 800 dEB diet. The apparent digestibility coefficient (ADC) of fat was unaffected by dEB, whereas the ADC of DM and protein were curvilinearly related to the dEB levels, being lowest and highest in the 200 and 800 dEB diets, respectively. Stomach chyme pH at 3 h after feeding was linearly related to the dEB levels (P< 0·05). At the same time, blood pH of the heart (P< 0·05) and caudal vein (P< 0·01) was curvilinearly related to the dEB levels, suggesting the influence of dEB on postprandial metabolic alkalosis. Consequently, maintenance energy expenditure (MEm) was curvilinearly related to the dEB levels (P< 0·001), being 54 % higher in the 800 dEB group (88 kJ/kg0·8per d) than in the 200 dEB group (57 kJ/kg0·8per d). These results suggest that varying dEB levels in a diet have both positive and negative effects on fish. On the one hand, they improve nutrient digestibility; on the other hand, they challenge the acid–base homeostasis (pH) of fish, causing an increase in MEm, and thereby reduce the energy required for growth.

Seaweed assemblages represent the dominant autotrophic biomass in many coastal environments, playing a central structural and functional role in several ecosystems. In Europe, seaweed assemblages are highly diverse systems. The combined seaweed flora of different European regions hold around 1550 species (belonging to nearly 500 genera), with new species continuously uncovered, thanks to the emergence of molecular tools. In this manuscript we review the effects of global and local stressors on European seaweeds, their communities, and ecosystem functioning. Following a brief review on the present knowledge on European seaweed diversity and distribution, and the role of seaweed communities in biodiversity and ecosystem functioning, we discuss the effects of biotic homogenization (invasive species) and global climate change (shifts in bioclimatic zones and ocean acidification) on the distribution of individual species and their effect on the structure and functioning of seaweed communities. The arrival of new introduced species (that already account for 5–10% of the European seaweeds) and the regional extirpation of native species resulting from oceans' climate change are creating new diversity scenarios with undetermined functional consequences. Anthropogenic local stressors create additional disruption often altering dramatically assemblage's structure. Hence, we discuss ecosystem level effects of such stressors like harvesting, trampling, habitat modification, overgrazing and eutrophication that impact coastal communities at local scales. Last, we conclude by highlighting significant knowledge gaps that need to be addressed to anticipate the combined effects of global and local stressors on seaweed communities. With physical and biological changes occurring at unexpected pace, marine phycologists should now integrate and join their research efforts to be able to contribute efficiently for the conservation and management of coastal systems.

Picoeukaryotes are a taxonomically diverse group of organisms less than 2 micrometers in diameter. Photosynthetic marine picoeukaryotes in the genus Micromonas thrive in ecosystems ranging from tropical to polar and could serve as sentinel organisms for biogeochemical fluxes of modern oceans during climate change. These broadly distributed primary producers belong to an anciently diverged sister clade to land plants. Although Micromonas isolates have high 18 S ribosomal RNA gene identity, we found that genomes from two isolates shared only 90% of their predicted genes. Their independent evolutionary paths were emphasized by distinct riboswitch arrangements as well as the discovery of intronic repeat elements in one isolate, and in metagenomic data, but not in other genomes. Divergence appears to have been facilitated by selection and acquisition processes that actively shape the repertoire of genes that are mutually exclusive between the two isolates differently than the core genes. Analyses of the Micromonas genomes offer valuable insights into ecological differentiation and the dynamic nature of early plant evolution.