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Anthropogenic emissions of carbon dioxide in the atmosphere have generated rapid variations in atmospheric composition which drives major climate changes. Climate change related effects include changes in physico-chemical proprieties of sea and freshwater, such as variations in water temperature, salinity, pH/pCO2 and oxygen content, which can impact fish critical physiological functions including reproduction. In this context, the main aim of the present review is to discuss how climate change related effects (variation in water temperature and salinity, increases in duration and frequency of hypoxia events, water acidification) would impact reproduction by affecting the neuroendocrine axis (brain-pituitary-gonad axis). Variations in temperature and photoperiod regimes are known to strongly affect sex differentiation and the timing and phenology of spawning period in several fish species. Temperature mainly acts at the level of gonad by interfering with steroidogenesis, (notably on gonadal aromatase activity) and gametogenesis. Temperature is also directly involved in the quality of released gametes and embryos development. Changes in salinity or water acidification are especially associated with reduction of sperm quality and reproductive output. Hypoxia events are able to interact with gonad steroidogenesis by acting on the steroids precursor cholesterol availability or directly on aromatase action, with an impact on the quality of gametes and reproductive success. Climate change related effects on water parameters likely influence also the reproductive behavior of fish. Although the precise mechanisms underlying the regulation of these effects are not always understood, in this review we discuss different hypothesis and propose future research perspectives.

We investigated how foot position and ankle arthrodesis affect the contact characteristics of the subtalar joint. Nine fresh-frozen specimens of amputated lower legs were used. Pressure-sensitive films were inserted into the anterior and posterior articulation of the subtalar joint. The contact areas and pressure for various foot positions and under axial loads of 600, 1200, and 1800 N were determined based on the gray level of the digitized film. In neutral position and under a 600 N load, the maximum contact pressure in the subtalar joint was 5.13 +/- 1.16 MPa. The contact area (1.18 +/- 0.35 cm2) was only 12.7% of the whole subtalar articulation area (9.31 +/- 0.66 cm2), and the total force (348.5 +/- 41.7 N) transmitted via this contact area was about 58% of the applied load (600 N). Dorsiflexion of the foot increased the contact area and the force transmitted, but decreased the average contact pressure in the subtalar joint, while the reverse occurred in plantar flexion. Eversion increased the subtalar contact stress, whereas inversion up to 10 degrees decreased it. Ankle joint arthrodesis shifted the contact areas in the subtalar joint posteriorly in all inversion/eversion positions. Moreover, total force transmitted through the subtalar joint as well as the contact pressure increased.

Riverine systems act as converging pathways for discarded litter within drainage basins, becoming key elements in gauging the transfer of mismanaged waste into the ocean. However, riverine litter data are scarce and biased towards microplastics, generally lacking information about larger items. Based on the first ever database of riverine floating macrolitter across Europe, we have estimated that between 307 and 925 million litter items are released annually from Europe into the ocean. The plastic fraction represented 82% of the observed litter, mainly fragments and single-use items (that is, bottles, packaging and bags). Our modelled estimates show that a major portion of the total litter loading is routed through small-sized drainage basins (<100 km2), indicating the relevance of small rivers, streams and coastal run-off. Moreover, the major contribution of high-income countries to the macrolitter inputs suggests that reducing ocean pollution cannot be achieved only by improving waste management, but also requires changing consumption habits and behaviour to curb waste generation at source. The inability of countries with well-developed recovery systems to control the leakage of waste into the environment further supports the need to regulate the production and use of plastic on a global scale. We acknowledge the additional members (coordinators and observers) of RiLON, listed in Supplementary Data 5, for their support in the field data collection and feedback during the data quality control. D.G.-F. was supported by the JRC institutional exploratory project RIMMEL (272346), PLASTREND (BBVA Foundation) and the European Union (H2020-MSCA-IF-2018 846843 - LitRivus). J.V. and C.M.-C. were supported by the MIDaS project (Spanish Ministry of Science, Innovation and Universities, CTM2016-77106-R, AEI/FEDER/UE). Peer reviewed

This repository contains the data associated with the paper Tedersoo et al. (2022) Global patterns in endemicity and vulnerability of soil fungi // Global Change Biology. DOI:10.1111/gcb.16398 Fungi are highly diverse organisms and provide a wealth of ecosystem functions. However, distribution patterns and conservation needs of fungi have been very little explored compared to charismatic animals and plants. Here we assess endemicity patterns, global change vulnerability and conservation priority areas for functional groups of soil fungi based on six global surveys using a high-resolution, long-read metabarcoding approach. Endemicity of all fungi and most functional groups peaks in tropical habitats, including Amazonia, Yucatan, West-Central Africa, Sri Lanka and New Caledonia, with a negligible island effect compared with plants and animals. We also found that fungi are vulnerable mostly to drought, heat and land cover change, particularly in dry tropical regions with high human population density. Fungal conservation areas of highest priority include herbaceous wetlands, tropical forests and woodlands. We suggest that there should be more attention focused on the conservation of fungi, especially tropical root symbiotic arbuscular mycorrhizal and ectomycorrhizal fungi, unicellular early-diverging groups and macrofungi in general. Given the low overlap between endemicity of fungi and macroorganisms, but high matching in conservation needs, detailed analyses on distribution and conservation requirements are warranted for other microorganisms and soil organisms in general. This repository contains the following data associated with the publication: Supplementary tables S1 - S6 (`Tables_S1-S6.xlsx`): - Table S1. Definition of ecoregions and assignment of samples to ecoregions - Table S2. GSMc dataset used for endemicity analyses - Table S3. Dataset used for modeling endemicity values - Table S4. Dataset used for calculating and mapping vulnerability scores - Table S5. Dataset used for calculating and mapping conservation value - Table S6. Additional funding sources by authors OTU distribution by samples and ecoregions (`Data_taxon_assignment_to ecoregions.xlsx`) Gridded maps: Conservation priorities for all fungi and fungal groups - ConservationPriority_AllFungi.tif - ConservationPriority_AM.tif - ConservationPriority_EcM.tif - ConservationPriority_Moulds.tif - ConservationPriority_NonEcMAgaricomycetes.tif - ConservationPriority_OHPs.tif - ConservationPriority_Pathogens.tif - ConservationPriority_Unicellular.tif - ConservationPriority_Yeasts.tif The average vulnerability of all fungi and fungal groups and the model uncertainty estimates - AverageVulnerability_AllFungi.tif - AverageVulnerability_AM.tif - AverageVulnerability_EcM.tif - AverageVulnerability_Moulds.tif - AverageVulnerability_NonEcMAgaricomycetes.tif - AverageVulnerability_OHPs.tif - AverageVulnerability_Pathogens.tif - AverageVulnerabilityUncertainty_AllFungi.tif - AverageVulnerabilityUncertainty_AM.tif - AverageVulnerabilityUncertainty_EcM.tif - AverageVulnerabilityUncertainty_Moulds.tif - AverageVulnerabilityUncertainty_NonEcMAgaricomycetes.tif - AverageVulnerabilityUncertainty_OHPs.tif - AverageVulnerabilityUncertainty_Pathogens.tif - AverageVulnerabilityUncertainty_Unicellular.tif - AverageVulnerabilityUncertainty_Yeasts.tif - AverageVulnerability_Unicellular.tif - AverageVulnerability_Yeasts.tif The relative importance of predicted vulnerability of all fungi - RelativeImportanceOfVulnerability_AllFungi.tif Vulnerability to drought, heat, and land cover change for all fungi - Vulnerability_AllFungi_Heat-Drought-LandCoverChange.tif - VulnerabilityUncertainty_AllFungi_Heat-Drought-LandCoverChange.tif Human footprint index based on the Land-Use Harmonisation (LUH2; Hurtt et al., 2020, doi:10.5194/gmd-13-5425-2020) - `LandCoverChange_1960-2015.tif` MD5 checksums for all files (`MD5.md5`) Fungal groups: - AM, arbuscular mycorrhizal fungi (including all Glomeromycota but excluding all Endogonomycetes) - EcM, ectomycorrhizal fungi (excluding dubious lineages) - NonEcMAgaricomycetes, non-EcM Agaricomycetes (mostly saprotrophic fungi with usually macroscopic fruiting bodies) - Moulds (including Mortierellales, Mucorales, Umbelopsidales and Aspergillaceae and Trichocomaceae of Eurotiales and Trichoderma of Hypocreales) - Putative pathogens (including plant, animal and fungal pathogens as primary or secondary lifestyles) - OHPs, opportunistic human parasites (excluding Mortierellales) - Yeasts (excluding dimorphic yeasts) - Unicellular, other unicellular (non-yeast) fungi (including chytrids, aphids, rozellids and other early-diverging fungal lineages) Detailed processing steps can be found here: https://github.com/Mycology-Microbiology-Center/Fungal_Endemicity_and_Vulnerability This repository contains the data associated with the paper Tedersoo et al. (2022) Global patterns in endemicity and vulnerability of soil fungi // Global Change Biology. DOI:10.1111/gcb.16398 Fungi are highly diverse organisms and provide a wealth of ecosystem functions. However, distribution patterns and conservation needs of fungi have been very little explored compared to charismatic animals and plants. Here we assess endemicity patterns, global change vulnerability and conservation priority areas for functional groups of soil fungi based on six global surveys using a high-resolution, long-read metabarcoding approach. Endemicity of all fungi and most functional groups peaks in tropical habitats, including Amazonia, Yucatan, West-Central Africa, Sri Lanka and New Caledonia, with a negligible island effect compared with plants and animals. We also found that fungi are vulnerable mostly to drought, heat and land cover change, particularly in dry tropical regions with high human population density. Fungal conservation areas of highest priority include herbaceous wetlands, tropical forests and woodlands. We suggest that there should be more attention focused on the conservation of fungi, especially tropical root symbiotic arbuscular mycorrhizal and ectomycorrhizal fungi, unicellular early-diverging groups and macrofungi in general. Given the low overlap between endemicity of fungi and macroorganisms, but high matching in conservation needs, detailed analyses on distribution and conservation requirements are warranted for other microorganisms and soil organisms in general.

In this study, the spatial and temporal patterns of the land cover were monitored within the Qazaly irrigation zone located in the deltaic zone of the Syrdarya river in the surroundings of the former Aral Sea. A 16-day MODIS (Moderate Resolution Imaging Spectroradiometer) Aqua NDVI (Normalized Difference Vegetation Index) data product with a spatial resolution of 250 meters was used for this purpose, covering the period between 2003 and 2018. Field survey results obtained in 2018 were used to build a sample dataset. The random forests supervised classification machine learning algorithm was used to map land cover, which produced good results with an overall accuracy of about 0.8. Statistics on land cover change were calculated and analyzed. The correctness of obtained classes was checked with Landsat 8 (OLI, The Operational Land Imager) images. Detailed land cover maps, including rice cropland, were derived. During the observation period, the rice croplands increased, while the generally irrigated area decreased.

In the Southern Ocean, several zooplankton taxonomic groups, euphausiids, copepods, salps and pteropods, are notable because of their biomass and abundance and their roles in maintaining food webs and ecosystem structure and function, including the provision of globally important ecosystem services. These groups are consumers of microbes, primary and secondary producers, and are prey for fishes, cephalopods, seabirds, and marine mammals. In providing the link between microbes, primary production, and higher trophic levels these taxa influence energy flows, biological production and biomass, biogeochemical cycles, carbon flux and food web interactions thereby modulating the structure and functioning of ecosystems. Additionally, Antarctic krill (Euphausia superba) and various fish species are harvested by international fisheries. Global and local drivers of change are expected to affect the dynamics of key zooplankton species, which may have potentially profound and wide-ranging implications for Southern Ocean ecosystems and the services they provide. Here we assess the current understanding of the dominant metazoan zooplankton within the Southern Ocean, including Antarctic krill and other key euphausiid, copepod, salp and pteropod species. We provide a systematic overview of observed and potential future responses of these taxa to a changing Southern Ocean and the functional relationships by which drivers may impact them. To support future ecosystem assessments and conservation and management strategies, we also identify priorities for Southern Ocean zooplankton research.

Abstract Marine plastic debris floating on the ocean surface is a major environmental problem. However, its distribution in the ocean is poorly mapped, and most of the plastic waste estimated to have entered the ocean from land is unaccounted for. Better understanding of how plastic debris is transported from coastal and marine sources is crucial to quantify and close the global inventory of marine plastics, which in turn represents critical information for mitigation or policy strategies. At the same time, plastic is a unique tracer that provides an opportunity to learn more about the physics and dynamics of our ocean across multiple scales, from the Ekman convergence in basin-scale gyres to individual waves in the surfzone. In this review, we comprehensively discuss what is known about the different processes that govern the transport of floating marine plastic debris in both the open ocean and the coastal zones, based on the published literature and referring to insights from neighbouring fields such as oil spill dispersion, marine safety recovery, plankton connectivity, and others. We discuss how measurements of marine plastics (both in situ and in the laboratory), remote sensing, and numerical simulations can elucidate these processes and their interactions across spatio-temporal scales.