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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Di Cintio, Antonio; Fernandes-Salvador, Jose Antonio; Puntila-Dodd, Riikka; Granado, Igor; +2 Authors

    A Bayesian network-based, user-friendly decision support tool modelling how different socioeconomic factors affect the effectiveness of a marine protected area. This is the model included in the paper "Socio-economic factors boosting the effectiveness of marine protected areas: a Bayesian network analysis".

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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    ZENODO
    Model . 2024
    License: CC BY
    Data sources: ZENODO
    ZENODO
    Model . 2024
    License: CC BY
    Data sources: Datacite
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      ZENODO
      Model . 2024
      License: CC BY
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      ZENODO
      Model . 2024
      License: CC BY
      Data sources: Datacite
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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Chust, Guillem; Villarino, Ernesto; McLean, Matthew; Mieszkowska, Nova; +34 Authors

    cti_cross_region_taxon This repository provides the data and codes used in the manuscript: Guillem Chust, Ernesto Villarino, Matthew McLean, Nova Mieszkowska, Lisandro Benedetti-Cecchi, Fabio Bulleri, Chiara Ravaglioli, Angel Borja, Iñigo Muxika, José A. Fernandes-Salvador, Leire Ibaibarriaga, Ainhize Uriarte, Marta Revilla, Fernando Villate, Arantza Iriarte, Ibon Uriarte, Soultana Zervoudaki, Jacob Carstensen, Paul J. Somerfield, Ana M. Queirós , Andrea J. McEvoy, Arnaud Auber, Manuel Hidalgo, Marta Coll, Joaquim Garrabou, Daniel Gómez-Gras, Cristina Linares, Francisco Ramírez, Núria Margarit, Mario Lepage, Chloé Dambrine, Jérémy Lobry, Myron A. Peck, Paula de la Barra, Anieke van Leeuwen, Gil Rilov, Erez Yeruham, Anik Brind'Amour, and Martin Lindegren. Cross-basin and cross-taxa patterns of marine community tropicalization and deborealization in warming European seas. Nature Communications Please check the github repo cti_cross_region_taxon for updates. Abstract Ocean warming and acidification, decreases in dissolved oxygen concentrations, and changes in primary production are causing an unprecedented global redistribution of marine life. The identification of underlying ecological processes underpinning marine species turnover, particularly the prevalence of tropicalization over deborealization, has been recently debated in the context of ocean warming. Here, we track changes in the mean thermal affinity of marine communities across European seas by calculating the Community Temperature Index for 65 biodiversity time series collected over four decades and containing 1,817 species from different communities (zooplankton, coastal benthos, pelagic and demersal invertebrates and fish). We show most communities and sites have clearly responded to ongoing ocean warming via abundance increases of warm-water species (tropicalization; 54%) and decreases of cold-water species (deborealization; 18%). Tropicalization dominated Atlantic sites compared to semi-enclosed basins such as the Mediterranean and Baltic Seas, probably due to physical barrier constraints to connectivity and species colonization. Semi-enclosed basins appeared to be particularly vulnerable to ocean warming, experiencing the fastest rates of warming and biodiversity loss through deborealization. Keywords: climate change, community temperature index, CTI, ocean connectivity. Acknowledgements This study has been supported by the European Union's Horizon 2020 research and innovation programme under grant agreement No 869300 (FutureMARES project) (G.C., E.V., J.F-S., M.P., M.Lin., C.D., D.G-G., G.R., L.B., C.R., M.C., F.R., G.R., P.B., M.P., M.Lep., J.L., A.B., N.M., J.G., F.B., L.B.C, A.Q., F.V., A.I., and I.U.), and by the Urban Klima 2050 -- LIFE 18 IPC 000001 project, which has been received funding from European Union's LIFE programme (G.C., E.V., L.I., A.B., A.U., and M.R.). Additional financial support was obtained from the Basque Government (PIBA2020-1-0028 & IT1723-22). We thank the NOAA Climate Prediction Center for providing Sea Temperature data through the NCEP Global Ocean Data Assimilation System (GODAS) www.cpc.ncep.noaa.gov/products/GODAS. We also thank Ocean Biodiversity Information System (OBIS) for providing global occurrences of the biological group studied here. Data from the Basque Country were obtained from the Basque Water Agency (URA) monitoring network, through a Convention with AZTI. M.C., J.G., D.G.-G. and F.R. acknowledge the 'Severo Ochoa Centre of Excellence' accreditation (CEX2019-000928-S). Authors M.H. and M.Lin. are grateful for the support from ICES Working Group on Comparative Ecosystem-based Analyses of Atlantic and Mediterranean marine systems (WGCOMEDA) for this research. This paper is contribution nº xxxx from AZTI, Marine Research, Basque Research and Technology Alliance (BRTA)

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    ZENODO
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    Authors: Zapata-Hernández, Germán; Gajardo-Rojas, Martina; Calderón-Seguel, Matías; Muñoz, Ariel A.; +5 Authors

    Advances and knowledge gaps on climate change impacts on honey bees and beekeeping: A systematic review

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    Authors: Schmechtig, Catherine; D'Ortenzio, Fabrizio; Carval, Thierry; Claustre, Hervé; +8 Authors

    Report providing recommendations for the data management and structure for the BGC extension at the European level.

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    ZENODO
    Other ORP type . 2022
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    ZENODO
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      ZENODO
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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Galgani, Luisa; Tzempelikou, Eleni; Kalantzi, Ioanna; Tsiola, Anastasia; +8 Authors

    Microplastics are substrates for microbial activity and can influence biomass production. This has potentially important implications at the sea-surface microlayer, the marine boundary layer that controls gas exchange with the atmosphere and where biologically produced organic compounds can accumulate. In the present study, we used large scale mesocosms (filled with 3 m3 of seawater) to simulate future ocean scenarios. We explored microbial organic matter dynamics in the sea-surface microlayer in the presence and absence of microplastic contamination of the underlying water. Our study shows that microplastics increased both biomass production and enrichment of particulate carbohydrates and proteins in the sea-surface microlayer. Importantly, this resulted in a 3% reduction in the concentration of dissolved CO2 in the underlying water. This reduction suggests direct and indirect impacts of microplastic pollution on the marine uptake of CO2, by modifying the biogenic composition of the sea’s boundary layer with the atmosphere.

    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ https://doi.org/10.5...arrow_drop_down
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    https://doi.org/10.5281/zenodo...
    Other ORP type . 2022
    License: CC BY
    Data sources: Sygma
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      https://doi.org/10.5281/zenodo...
      Other ORP type . 2022
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    Authors: Vries, Joost; Monteiro, Fanny; Wheeler, Glen; Poulton, Alex; +5 Authors

    Coccolithophores are globally important marine calcifying phytoplankton that utilize a haplo-diplontic life cycle. The haplo-diplontic life cycle allows coccolithophores to divide in both life cycle phases and potentially expands coccolithophore niche volume. Research has, however, to date largely overlooked the life cycle of coccolithophores and has instead focused on the diploid life cycle phase of coccolithophores. Through the synthesis and analysis of global scanning electron microscopy (SEM) coccolithophore abundance data (n=2534), we find that calcified haploid coccolithophores generally constitute a minor component of the total coccolithophore abundance (≈ 2 %–15 % depending on season). However, using case studies in the Atlantic Ocean and Mediterranean Sea, we show that, depending on environmental conditions, calcifying haploid coccolithophores can be significant contributors to the coccolithophore standing stock (up to ≈30 %). Furthermore, using hypervolumes to quantify the niche of coccolithophores, we illustrate that the haploid and diploid life cycle phases inhabit contrasting niches and that on average this allows coccolithophores to expand their niche by ≈18.8 %, with a range of 3 %–76 % for individual species. Our results highlight that future coccolithophore research should consider both life cycle stages, as omission of the haploid life cycle phase in current research limits our understanding of coccolithophore ecology. Our results furthermore suggest a different response to nutrient limitation and stratification, which may be of relevance for further climate scenarios. Our compilation highlights the spatial and temporal sparsity of SEM measurements and the need for new molecular techniques to identify uncalcified haploid coccolithophores. Our work also emphasizes the need for further work on the carbonate chemistry niche of the coccolithophore life cycle.

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  • Authors: Corgnati; L.;

    The applications are designed for High Frequency Radar (HFR) data management according to the European HFR node processing workflow, thus generating aggregated radial and total velocity files in netCDF format according to the European standard data and metadata model for near real time HFR current data. These applications implement the periodic temporal aggregation of the datasets and the related CDI metadata to be distributed via SeaDataCloud. These applications are designed for the centralized run at the EU HFR Node.

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    Authors: Clyne, Margot; Lamarque, Jean-Francois; Mills, Michael J.; Khodri, Myriam; +19 Authors

    As part of the Model Intercomparison Project on the climatic response to Volcanic forcing (VolMIP), several climate modeling centers performed a coordinated pre-study experiment with interactive stratospheric aerosol models simulating the volcanic aerosol cloud from an eruption resembling the 1815 Mt. Tambora eruption (VolMIP-Tambora ISA ensemble). The pre-study provided the ancillary ability to assess intermodel diversity in the radiative forcing for a large stratospheric-injecting equatorial eruption when the volcanic aerosol cloud is simulated interactively. An initial analysis of the VolMIP-Tambora ISA ensemble showed large disparities between models in the stratospheric global mean aerosol optical depth (AOD). In this study, we now show that stratospheric global mean AOD differences among the participating models are primarily due to differences in aerosol size, which we track here by effective radius. We identify specific physical and chemical processes that are missing in some models and/or parameterized differently between models, which are together causing the differences in effective radius. In particular, our analysis indicates that interactively tracking hydroxyl radical (OH) chemistry following a large volcanic injection of sulfur dioxide (SO2) is an important factor in allowing for the timescale for sulfate formation to be properly simulated. In addition, depending on the timescale of sulfate formation, there can be a large difference in effective radius and subsequently AOD that results from whether the SO2 is injected in a single model grid cell near the location of the volcanic eruption, or whether it is injected as a longitudinally averaged band around the Earth.

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    Authors: giovanni ardito;
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  • Authors: Maffezzoli, Niccolo; Vallelonga, Paul T; Edwards, Ross; Saiz-Lopez, Alfonso; +5 Authors

    Concentrations of sodium (Na), bromine (Br), calcium (Ca), magnesium (Mg) and chlorine (Cl) measured in the 2015 RECAP ice core by inductive coupled plasma mass spectroscopy (ICPMS) along the 120,000 year-record, as well as the sea-salt sodium (ssNa) calculations are presented. In the 0-8 kyr b2015 section only the Br and Na series are presented, as 100-yr averages.

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    Authors: Di Cintio, Antonio; Fernandes-Salvador, Jose Antonio; Puntila-Dodd, Riikka; Granado, Igor; +2 Authors

    A Bayesian network-based, user-friendly decision support tool modelling how different socioeconomic factors affect the effectiveness of a marine protected area. This is the model included in the paper "Socio-economic factors boosting the effectiveness of marine protected areas: a Bayesian network analysis".

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    Authors: Chust, Guillem; Villarino, Ernesto; McLean, Matthew; Mieszkowska, Nova; +34 Authors

    cti_cross_region_taxon This repository provides the data and codes used in the manuscript: Guillem Chust, Ernesto Villarino, Matthew McLean, Nova Mieszkowska, Lisandro Benedetti-Cecchi, Fabio Bulleri, Chiara Ravaglioli, Angel Borja, Iñigo Muxika, José A. Fernandes-Salvador, Leire Ibaibarriaga, Ainhize Uriarte, Marta Revilla, Fernando Villate, Arantza Iriarte, Ibon Uriarte, Soultana Zervoudaki, Jacob Carstensen, Paul J. Somerfield, Ana M. Queirós , Andrea J. McEvoy, Arnaud Auber, Manuel Hidalgo, Marta Coll, Joaquim Garrabou, Daniel Gómez-Gras, Cristina Linares, Francisco Ramírez, Núria Margarit, Mario Lepage, Chloé Dambrine, Jérémy Lobry, Myron A. Peck, Paula de la Barra, Anieke van Leeuwen, Gil Rilov, Erez Yeruham, Anik Brind'Amour, and Martin Lindegren. Cross-basin and cross-taxa patterns of marine community tropicalization and deborealization in warming European seas. Nature Communications Please check the github repo cti_cross_region_taxon for updates. Abstract Ocean warming and acidification, decreases in dissolved oxygen concentrations, and changes in primary production are causing an unprecedented global redistribution of marine life. The identification of underlying ecological processes underpinning marine species turnover, particularly the prevalence of tropicalization over deborealization, has been recently debated in the context of ocean warming. Here, we track changes in the mean thermal affinity of marine communities across European seas by calculating the Community Temperature Index for 65 biodiversity time series collected over four decades and containing 1,817 species from different communities (zooplankton, coastal benthos, pelagic and demersal invertebrates and fish). We show most communities and sites have clearly responded to ongoing ocean warming via abundance increases of warm-water species (tropicalization; 54%) and decreases of cold-water species (deborealization; 18%). Tropicalization dominated Atlantic sites compared to semi-enclosed basins such as the Mediterranean and Baltic Seas, probably due to physical barrier constraints to connectivity and species colonization. Semi-enclosed basins appeared to be particularly vulnerable to ocean warming, experiencing the fastest rates of warming and biodiversity loss through deborealization. Keywords: climate change, community temperature index, CTI, ocean connectivity. Acknowledgements This study has been supported by the European Union's Horizon 2020 research and innovation programme under grant agreement No 869300 (FutureMARES project) (G.C., E.V., J.F-S., M.P., M.Lin., C.D., D.G-G., G.R., L.B., C.R., M.C., F.R., G.R., P.B., M.P., M.Lep., J.L., A.B., N.M., J.G., F.B., L.B.C, A.Q., F.V., A.I., and I.U.), and by the Urban Klima 2050 -- LIFE 18 IPC 000001 project, which has been received funding from European Union's LIFE programme (G.C., E.V., L.I., A.B., A.U., and M.R.). Additional financial support was obtained from the Basque Government (PIBA2020-1-0028 & IT1723-22). We thank the NOAA Climate Prediction Center for providing Sea Temperature data through the NCEP Global Ocean Data Assimilation System (GODAS) www.cpc.ncep.noaa.gov/products/GODAS. We also thank Ocean Biodiversity Information System (OBIS) for providing global occurrences of the biological group studied here. Data from the Basque Country were obtained from the Basque Water Agency (URA) monitoring network, through a Convention with AZTI. M.C., J.G., D.G.-G. and F.R. acknowledge the 'Severo Ochoa Centre of Excellence' accreditation (CEX2019-000928-S). Authors M.H. and M.Lin. are grateful for the support from ICES Working Group on Comparative Ecosystem-based Analyses of Atlantic and Mediterranean marine systems (WGCOMEDA) for this research. This paper is contribution nº xxxx from AZTI, Marine Research, Basque Research and Technology Alliance (BRTA)

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    Authors: Zapata-Hernández, Germán; Gajardo-Rojas, Martina; Calderón-Seguel, Matías; Muñoz, Ariel A.; +5 Authors

    Advances and knowledge gaps on climate change impacts on honey bees and beekeeping: A systematic review

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    Authors: Schmechtig, Catherine; D'Ortenzio, Fabrizio; Carval, Thierry; Claustre, Hervé; +8 Authors

    Report providing recommendations for the data management and structure for the BGC extension at the European level.

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    Authors: Galgani, Luisa; Tzempelikou, Eleni; Kalantzi, Ioanna; Tsiola, Anastasia; +8 Authors

    Microplastics are substrates for microbial activity and can influence biomass production. This has potentially important implications at the sea-surface microlayer, the marine boundary layer that controls gas exchange with the atmosphere and where biologically produced organic compounds can accumulate. In the present study, we used large scale mesocosms (filled with 3 m3 of seawater) to simulate future ocean scenarios. We explored microbial organic matter dynamics in the sea-surface microlayer in the presence and absence of microplastic contamination of the underlying water. Our study shows that microplastics increased both biomass production and enrichment of particulate carbohydrates and proteins in the sea-surface microlayer. Importantly, this resulted in a 3% reduction in the concentration of dissolved CO2 in the underlying water. This reduction suggests direct and indirect impacts of microplastic pollution on the marine uptake of CO2, by modifying the biogenic composition of the sea’s boundary layer with the atmosphere.

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    https://doi.org/10.5281/zenodo...
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    Authors: Vries, Joost; Monteiro, Fanny; Wheeler, Glen; Poulton, Alex; +5 Authors

    Coccolithophores are globally important marine calcifying phytoplankton that utilize a haplo-diplontic life cycle. The haplo-diplontic life cycle allows coccolithophores to divide in both life cycle phases and potentially expands coccolithophore niche volume. Research has, however, to date largely overlooked the life cycle of coccolithophores and has instead focused on the diploid life cycle phase of coccolithophores. Through the synthesis and analysis of global scanning electron microscopy (SEM) coccolithophore abundance data (n=2534), we find that calcified haploid coccolithophores generally constitute a minor component of the total coccolithophore abundance (≈ 2 %–15 % depending on season). However, using case studies in the Atlantic Ocean and Mediterranean Sea, we show that, depending on environmental conditions, calcifying haploid coccolithophores can be significant contributors to the coccolithophore standing stock (up to ≈30 %). Furthermore, using hypervolumes to quantify the niche of coccolithophores, we illustrate that the haploid and diploid life cycle phases inhabit contrasting niches and that on average this allows coccolithophores to expand their niche by ≈18.8 %, with a range of 3 %–76 % for individual species. Our results highlight that future coccolithophore research should consider both life cycle stages, as omission of the haploid life cycle phase in current research limits our understanding of coccolithophore ecology. Our results furthermore suggest a different response to nutrient limitation and stratification, which may be of relevance for further climate scenarios. Our compilation highlights the spatial and temporal sparsity of SEM measurements and the need for new molecular techniques to identify uncalcified haploid coccolithophores. Our work also emphasizes the need for further work on the carbonate chemistry niche of the coccolithophore life cycle.

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  • Authors: Corgnati; L.;

    The applications are designed for High Frequency Radar (HFR) data management according to the European HFR node processing workflow, thus generating aggregated radial and total velocity files in netCDF format according to the European standard data and metadata model for near real time HFR current data. These applications implement the periodic temporal aggregation of the datasets and the related CDI metadata to be distributed via SeaDataCloud. These applications are designed for the centralized run at the EU HFR Node.

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    Authors: Clyne, Margot; Lamarque, Jean-Francois; Mills, Michael J.; Khodri, Myriam; +19 Authors

    As part of the Model Intercomparison Project on the climatic response to Volcanic forcing (VolMIP), several climate modeling centers performed a coordinated pre-study experiment with interactive stratospheric aerosol models simulating the volcanic aerosol cloud from an eruption resembling the 1815 Mt. Tambora eruption (VolMIP-Tambora ISA ensemble). The pre-study provided the ancillary ability to assess intermodel diversity in the radiative forcing for a large stratospheric-injecting equatorial eruption when the volcanic aerosol cloud is simulated interactively. An initial analysis of the VolMIP-Tambora ISA ensemble showed large disparities between models in the stratospheric global mean aerosol optical depth (AOD). In this study, we now show that stratospheric global mean AOD differences among the participating models are primarily due to differences in aerosol size, which we track here by effective radius. We identify specific physical and chemical processes that are missing in some models and/or parameterized differently between models, which are together causing the differences in effective radius. In particular, our analysis indicates that interactively tracking hydroxyl radical (OH) chemistry following a large volcanic injection of sulfur dioxide (SO2) is an important factor in allowing for the timescale for sulfate formation to be properly simulated. In addition, depending on the timescale of sulfate formation, there can be a large difference in effective radius and subsequently AOD that results from whether the SO2 is injected in a single model grid cell near the location of the volcanic eruption, or whether it is injected as a longitudinally averaged band around the Earth.

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    Authors: giovanni ardito;
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  • Authors: Maffezzoli, Niccolo; Vallelonga, Paul T; Edwards, Ross; Saiz-Lopez, Alfonso; +5 Authors

    Concentrations of sodium (Na), bromine (Br), calcium (Ca), magnesium (Mg) and chlorine (Cl) measured in the 2015 RECAP ice core by inductive coupled plasma mass spectroscopy (ICPMS) along the 120,000 year-record, as well as the sea-salt sodium (ssNa) calculations are presented. In the 0-8 kyr b2015 section only the Br and Na series are presented, as 100-yr averages.

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    Other ORP type . 2020
    Data sources: CNR ExploRA
    CNR ExploRA
    Other ORP type . 2020
    Data sources: CNR ExploRA
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      Other ORP type . 2020
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      CNR ExploRA
      Other ORP type . 2020
      Data sources: CNR ExploRA