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Assessing the impacts of disturbance over large areas and long time periods is crucial for nature management, but also challenging since impacts depend on both wildlife responses to disturbance and on the spatiotemporal distribution of disturbance sources. Combined tracking of animals and disturbance sources enables quantification of wildlife responses as a function of the distance to a disturbance source. We provide a framework to derive such distance–response curves and combine those with disturbance source presence data to quantify energetic costs of disturbance at a landscape scale. We tracked 90 Eurasian Oystercatchers Haematopus ostralegus and all aircraft in a military training area in the Dutch Wadden Sea. We quantified distance–response curves estimating flight probability and additional displacement for five types of aircraft activities, by comparing bird movement prior to aircraft presence with movement during aircraft presence. We then used the distance–response curves to map mean and variation in additional daily energy expenditure due to cumulative aircraft disturbance across the landscape for a 700-day period. Flight probability and displacement responses differed strongly among aircraft activities and decreased from transport aeroplanes, through bombing jets, helicopters, jets to small civil aeroplanes. Since the most disturbing aircraft activities were also the rarest ones, mean additional daily energy expenditure did not exceed 0.25%. However, days with substantial (>1%) additional expenditure occurred between 0.1% and 3.7% of all days across high-tide roosts in the tidal basin. Notably, expenditure particularly spiked on days with transport aeroplane activity (up to 8.5%). Synthesis and applications. We quantified cumulative energetic flight costs due to aircraft disturbance and found that these were low and unlikely to impact survival of oystercatchers in our study area. Our results provide evidence that the legal minimum flight height of 450 m for small civil aeroplanes effectively limits ...

Local biodiversity trends over time are likely to be decoupled from global trends, as local processes may compensate or counteract global change. We analyze 161 long-term biological time series (15-91 years) collected across Europe, using a comprehensive dataset comprising similar to 6,200 marine, freshwater and terrestrial taxa. We test whether (i) local long-term biodiversity trends are consistent among biogeoregions, realms and taxonomic groups, and (ii) changes in biodiversity correlate with regional climate and local conditions. Our results reveal that local trends of abundance, richness and diversity differ among biogeoregions, realms and taxonomic groups, demonstrating that biodiversity changes at local scale are often complex and cannot be easily generalized. However, we find increases in richness and abundance with increasing temperature and naturalness as well as a clear spatial pattern in changes in community composition (i.e. temporal taxonomic turnover) in most biogeoregions of Northern and Eastern Europe. The global biodiversity decline might conceal complex local and group-specific trends. Here the authors report a quantitative synthesis of longterm biodiversity trends across Europe, showing how, despite overall increase in biodiversity metric and stability in abundance, trends differ between regions, ecosystem types, and taxa. ; Y We are grateful to the ILTER network and the eLTER PLUS project (Grand Agreement No. 871128) for financial support. We acknowledge the E-OBS dataset from the EUFP6 project ENSEMBLES (http://ensembles-eu.metoffice.com) and the data providers in the ECA&D project (http://www.ecad.eu).The evaluation of forest plant diversity was based on data collected by partners of the official UNECE ICP Forests Network (http://icp-forests.net/contributors); part of the data were co-financed by the European Commission, project LIFE 07 ENV/D/000218 "Further Development and Implementation of an EU-level Forest monitoring Systeme (FutMon)". Data on wintering water birds in Bulgaria were provided by the national Executive Environment Agency with the Ministry of Environment and Waters. Data from the Finnish moth monitoring scheme were supported by the Finnish Ministry of the Environment. Data from the Swedish ICP Integrated Monitoring sites were financed by the Swedish Environmental Protection Agency. Data collection at Esthwaite Water and a subset of UK ECN sites was supported by Natural Environment Research Council award number NE/R016429/1 as part of the UK-SCaPE programme delivering National Capability. Sponsorship of other UK ECN sites contributing data was provided by Agri-Food and Biosciences Institute, Biotechnology and Biological Sciences Research Council, Department of Environment Food and Rural Affairs, Natural Resources Wales, Defense Science Technology Laboratory, Environment Agency, Forestry Commission, Forest Research, the James Hutton Institute (The Rural & Environment Science & Analytical Services Division of the Scottish Government), Natural England, Rothamsted Research, Scottish Government, Scottish Natural Heritage and the Welsh Government. Data from the Mondego estuary (Portugal) were supported by the Centre for Functional Ecology Strategic Project (UID/BIA/04004/2019) within the PT2020 Partnership Agreement and COMPETE 2020, and by FEDER through the project ReNATURE (Centro 2020, Centro-01-765-0145-FEDER-000007). We would like to thank Limburgse Koepel voor Natuurstudie (LiKoNa) for the data related to the National Park Hoge Kempen (BE). We would like to acknowledge the support for the long-term monitoring program MONEOS in the Scheldt estuary (BE) by `De Vlaamse Waterweg' and `Maritieme Toegang' (Flemish government). We are grateful to the board of the National Park "De Hoge Veluwe" for the permission to conduct our research on their property. We thank Ian J. Winfield and Terje Bongard for contributing data for the sites: Bassenthwaite Lake, Derwent Water (UK) and Atna River (Norway, freshwater invertebrate time series). Open access funding provided by Umea University. ; Pilotto, F; Haase, P (corresponding author), Senckenberg Res Inst, Gelnhausen, Germany; Nat Hist Museum, Gelnhausen, Germany; Univ Duisburg Essen, Essen, Germany. francesca.pilotto@umu.se; francesca.pilotto@umu.se

Este artículo contiene 11 páginas, 2 tablas, 4 figuras. ; Local biodiversity trends over time are likely to be decoupled from global trends, as local processes may compensate or counteract global change. We analyze 161 long-term biological time series (15–91 years) collected across Europe, using a comprehensive dataset comprising ~6,200 marine, freshwater and terrestrial taxa. We test whether (i) local long-term biodiversity trends are consistent among biogeoregions, realms and taxonomic groups, and (ii) changes in biodiversity correlate with regional climate and local conditions. Our results reveal that local trends of abundance, richness and diversity differ among biogeoregions, realms and taxonomic groups, demonstrating that biodiversity changes at local scale are often complex and cannot be easily generalized. However, we find increases in richness and abundance with increasing temperature and naturalness as well as a clear spatial pattern in changes in community composition (i.e. temporal taxonomic turnover) in most biogeoregions of Northern and Eastern Europe. ; We are grateful to the ILTER network and the eLTER PLUS project (Grand Agreement No. 871128) for financial support. We acknowledge the E-OBS dataset from the EUFP6 project ENSEMBLES (http://ensembles-eu.metoffice.com) and the data providers in the ECA&D project (http://www.ecad.eu). The evaluation of forest plant diversity was based on data collected by partners of the official UNECE ICP Forests Network (http://icp-forests.net/contributors); part of the data were co-financed by the European Commission, project LIFE 07 ENV/D/000218 "Further Development and Implementation of an EU-level Forest monitoring Systeme (FutMon)". Data on wintering water birds in Bulgaria were provided by the national Executive Environment Agency with the Ministry of Environment and Waters. Data from the Finnish moth monitoring scheme were supported by the Finnish Ministry of the Environment. Data from the Swedish ICP Integrated Monitoring sites were financed by the Swedish Environmental Protection Agency. Data collection at Esthwaite Water and a subset of UK ECN sites was supported by Natural Environment Research Council award number NE/ R016429/1 as part of the UK-SCaPE programme delivering National Capability. Sponsorship of other UK ECN sites contributing data was provided by Agri-Food and Biosciences Institute, Biotechnology and Biological Sciences Research Council, Department of Environment Food and Rural Affairs, Natural Resources Wales, Defense Science Technology Laboratory, Environment Agency, Forestry Commission, Forest Research, the James Hutton Institute (The Rural & Environment Science & Analytical Services Division of the Scottish Government), Natural England, Rothamsted Research, Scottish Government, Scottish Natural Heritage and the Welsh Government. Data from the Mondego estuary (Portugal) were supported by the Centre for Functional Ecology Strategic Project (UID/BIA/04004/2019) within the PT2020 Partnership Agreement and COMPETE 2020, and by FEDER through the project ReNATURE (Centro 2020, Centro-01-765-0145-FEDER-000007). We would like to thank Limburgse Koepel voor Natuurstudie (LiKoNa) for the data related to the National Park Hoge Kempen (BE). We would like to acknowledge the support for the long-term monitoring program MONEOS in the Scheldt estuary (BE) by 'De Vlaamse Waterweg' and 'Maritieme Toegang' (Flemish government). We are grateful to the board of the National Park "De Hoge Veluwe" for the permission to conduct our research on their property. We thank Ian J. Winfield and Terje Bongard for contributing data for the sites: Bassenthwaite Lake, Derwent Water (UK) and Atna River (Norway, freshwater invertebrate time series). Open access funding provided by Umeå University. ; Peer reviewed