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1. Aphids are abundant in natural and managed vegetation, supporting a diverse community of organisms and causing damage to agricultural crops. Due to a changing climate, periods of drought are anticipated to increase, and the potential consequences of this for aphid-plant interactions are unclear. 2. Using a meta-analysis and synthesis approach, we aimed to advance understanding of how increased drought incidence will affect this ecologically and economically important insect group, and to characterise any potential underlying mechanisms. We used qualitative and quantitative synthesis techniques to determine whether drought stress has a negative, positive, or null effect on aphid fitness and examined these effects in relation to 1) aphid biology, 2) geographical region, 3) host plant biology. 3. Across all studies, aphid fitness is typically reduced under drought. Subgroup analysis detected no difference in relation to aphid biology, geographical region, or the aphid-plant combination, indicating the negative effect of drought on aphids is potentially universal. Furthermore, drought stress had a negative impact on plant vigour and increased plant concentrations of defensive chemicals, suggesting the observed response of aphids is associated with reduced plant vigour and increased chemical defence in drought-stressed plants. 4. We propose a conceptual model to predict drought effects on aphid fitness in relation to plant vigour and defence to stimulate further research. Please check the ReadMe for an explanation of the values included in the dataset. Please note that n/a values are included in the Global_Dataset tab for plant meta-analysis data (_Plant_Vigour, _Plant_Defence, and _Plant_Nutrition), these indicate studies that did not report these parameters. Data was collected and curated using standard systematic literature synthesis approaches. The effect size (Hedges' g) reported in the dataset was calculated from extracted means and standard deviations.

Detailed measurements on soil, plant and atmosphere are required for the development and validation of crop growth and agroecosystem models. These measurements should be available with a high temporal resolution. With the aim of creating a growth model for winter wheat, an experiment with winter wheat under integrated cultivation conditions was carried out at the intensive experimental field of the Müncheberg Research Centre for Soil Fertility, Germany, between 1979 and 1981, both with and without irrigation. Field chambers were used for daily measurements of the CO2 balance of the crop stand. The daily evaporation was measured with two different evaporation pans. The different biomass components of the winter wheat crop stand were measured in weekly intervals from April to harvest in July/August. The different biomass components were analysed in the laboratory concerning their carbon, nitrogen, phosphorus and potassium content. Based on this coherent data set, the growth model TRITSIM for winter wheat was developed at the Müncheberg Research Centre for Soil Fertility in the 1980s. TRITSIM was incorporated into the complex agroecosystem model AGROSIM-WHEAT of the Research Institute of Plant Protection Eberswalde, Germany, for the identification of optimal plant protection measures under practical field conditions. The data set presented here can also be the basis for the verification and validation of further winter wheat growth and/or agroecosystem models.

Environmental dataBioclimatic data and environmental data for all 56 European peatland site (geo referenced by longitude [long], latitude [lat] and altitude [ALT]. MAT = Mean annual temperature (°C), TS = Seasonality in temperature, MAP = Mean annual precipitation (mm), PS = Seasonality in precipitation, tot_sox = Total sulphur deposition SOx (mg m-2 yr-1), tot_noy = Total oxidized nitrogen deposition (mg m-2 yr-1), tot_nhx = Total reduced nitrogen deposition (mg m-2), PT warm = Lang’s moisture index. The four bioclimatic variables (MAT, TS, MAP, PS) were extracted from the WorldClim database (Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. & Jarvis, A. Very high resolution interpolated climate surfaces for global land areas. Int. J. Climatol. 25, 1965–1978 (2005)), and averaged over the 2000-2009 period. Atmospheric deposition data were produced using the EMEP (European Monitoring and Evaluation Programme)-based IDEM (Integrated Deposition Model) model (Pieterse, G., Bleeker, A., Vermeulen, A. T., Wu, Y. & Erisman, J. W. High resolution modelling of atmosphere‐canopy exchange of acidifying and eutrophying components and carbon dioxide for European forests. Tellus B 59, 412–424 (2007)) and consisted of grid cell averages of total reduced (NHx) and oxidised (NOy) nitrogen and sulphur (SOx) deposition. The moisture index (PTwarm) was calculated as the ratio between mean precipitation and mean temperature in the warmest quarter (Thornwaite, C. W. & Holzman, B. Measurement of evaporation from land and water surfaces. USDA Technical Bulletin 817, 1–143 (1942))Data 1_environmental data.txtplant community dataAbundance data (% cover) for all vascular plant and bryophyte species from five randomly chosen hummocks and lawns (0.25 m2 quadrats; ten in total) across 56 European Sphagnum-dominated peatlands were collected in two consecutive summers (2010 and 2011). Vascular plants and Sphagnum mosses were identified to the species level. Non-Sphagnum bryophytes were identified to the family level. Lichens were recorded as one group.Data 2_plant community data.txttraits vascular plantsPlant functional traits used to calculate functional indices for the vascular plant communities. Traits were extracted from LEDA (Kleyer, M. et al. The LEDA Traitbase: a database of life‐history traits of the Northwest European flora. J. Ecol. 96, 1266–1274 (2008)). Only trait data available for all species our data-set were extracted.ncomms_Data 3_traits vascular plants.txttraits SphagnumTrait values (means) for Sphagnum spp. C = tissue carbon content (mg g-1), N = tissue nitrogen content (mg g-1), P = tissue phosphorus content (mg g-1), Productivity ( St.w = stem width (mm), l.h.c. = length hyaline cells (µm), w.h.c. = width hyaline cells (µm), l.s.l. = length stem leaves (mm), w.s.l. = width stem leaves. These measured traits were complemented with traits extracted from the literature. These latter traits included plant length (Hill, M. O., Preston, C. D., Bosanquet, S. & Roy, D. B. BRYOATT: attributes of British and Irish mosses, liverworts and hornworts. Centre for Ecology & Hydrology, Huntingdon, UK (2007)), spore diameter and capsule diameter (Sundberg, S., Hansson, J. & Rydin, H. Colonization of Sphagnum on land uplift islands in the Baltic Sea: time, area, distance and life history. Journal of Biogeography 33, 1479–1491 (2006)), productivity (Gunnarsson, U. Global patterns of Sphagnum productivity. J. Bryol. 27, 269–279 (2005))ncomms_Data 4_traits Sphagnum.txt In peatland ecosystems, plant communities mediate a globally significant carbon store. The effects of global environmental change on plant assemblages are expected to be a factor in determining how ecosystem functions such as carbon uptake will respond. Using vegetation data from 56 Sphagnum-dominated peat bogs across Europe, we show that in these ecosystems plant species aggregate into two major clusters that are each defined by shared response to environmental conditions. Across environmental gradients, we find significant taxonomic turnover in both clusters. However, functional identity and functional redundancy of the community as a whole remain unchanged. This strongly suggests that in peat bogs, species turnover across environmental gradients is restricted to functionally similar species. Our results demonstrate that plant taxonomic and functional turnover are decoupled, which may allow these peat bogs to maintain ecosystem functioning when subject to future environmental change.

The aim of this study was to quantify direct and indirect relationships between soil microbial community properties (potential basal respiration, microbial biomass) and abiotic factors (soil, climate) in three major land-cover types. Location: Europe Time period: 2018 Major taxa studied: Microbial community (fungi and bacteria) We collected 881 soil samples from across Europe in the framework of the Land Use/Land Cover Area Frame Survey (LUCAS). We measured potential soil basal respiration at 20ºC and microbial biomass (substrate-induced respiration) using an O2-microcompensation apparatus. Climate and soil data were obtained from previous LUCAS surveys and online databases. Structural equation modeling (SEM) was used to quantify relationships between variables, and equations extracted from SEMs were used to create predictive maps. Fatty acid methyl esters were measured in a subset of samples to distinguish fungal from bacterial biomass. Soil microbial properties in croplands were more heavily affected by climate variables than those in forests. Potential soil basal respiration and microbial biomass were correlated in forests but decoupled in grasslands and croplands, where microbial biomass depended on soil carbon. Forests had a higher ratio of fungi to bacteria than grasslands or croplands. Soil microbial communities in grasslands and croplands are likely carbon-limited in comparison with those in forests, and forests have a higher dominance of fungi indicating differences in microbial community composition. Notably, the often already-degraded soils of croplands could be more vulnerable to climate change than more natural soils. The provided maps show potentially vulnerable areas that should be explicitly accounted for in coming management plans to protect soil carbon and slow the increasing vulnerability of European soils to climate change. [Methods] Soil samples were collected during the 2018 LUCAS soil sampling campaign. Soil chemical and physical properties were measured at the Joint Research Centre in Ispra, Italy (Orgiazzi et al., 2018). Soil microbial respiration and biomass, as well as water content and water holding capacity, were measured in the Eisenhauer lab of the German Centre for Integrative Biodiversity Research. Fungi/Bacteria was measured by fatty acid analysis by Felipe Bastida at CEBAS CSIC. Climate and geographical data were harvested from various databases, which are listed in Appendix 1 (data sources) of the associated paper. For more details on the soil sampling and physical and chemical properties, see: Orgiazzi, A., Ballabio, C., Panagos, P., Jones, A., & Fernández-Ugalde, O. (2018). LUCAS Soil, the largest expandable soil dataset for Europe: a review. European Journal of Soil Science, 69(1), 140-153. https://doi.org/10.1111/ejss.12499 For more details on the measurements of soil microbial respiration and biomass, fatty acids, and water holding capacity, see the supplementary methods of the associated paper (Appendix 2). [Usage Notes] Fatty acid analysis was performed for a subset of 267 samples. Water holding capacity and associated measurements of basal respiration was analyzed in a subset of 100 samples. The samples that were not in these subsets have NA values for the columns associated with these measurements. In order to protect the precise locations of the LUCAS sampling sites, latitude and longitude values could not be given. The approximate location of each sampling site is instead described by the NUTS3 region. If you wish to replicate the structural equation modeling described in the paper, for which latitude is required, please get in touch. A description of each column is available in the associated metadata file. Deutsche Forschungsgemeinschaft, Award: FZT 118-202548816. European Research Council, Award: 694368. European Commission. Directorate-General for the Environment. Direction Générale Opérationnelle Agriculture, Ressources Naturelles et Environnement du Service Public de Wallonie. Eurostat. Peer reviewed

Mit einem Anteil von rund 30% am Endenergieverbrauch und etwa 20% an den CO2-Emissionen haben private Haushalte in Deutschland einen großen Einfluss auf die Umwelt. Gleichzeitig sind private Haushalte ein zentraler Adressat für politische Interventionen zur Bekämpfung des Klimawandels. Vor diesem Hintergrund hat die Politik zahlreiche Maßnahmen zur Verringerung des Energiekonsums und zur Förderung regenerativer Energietechnologien ergriffen. Diese politischen Maßnahmen bedürfen einer sorgfältigen Evaluierung ihrer Effektivität und Kosteneffizienz, um kostspielige Redundanzen durch sich überlappende Instrumente zu vermeiden. Eine solche Evaluation umwelt- und energiepolitischer Maßnahmen erfordert eine umfangreiche Datenbasis. Besonders im Bereich der privaten Haushalte waren solche Daten in Deutschland bislang nicht verfügbar. Die Reagibilität deutscher Haushalte auf Maßnahmen zur Bekämpfung des Klimawandels war daher weitgehend unbekannt. Das Sozial-Ökologische Panel stellt zu diesem Zweck umfangreiche, frei verfügbare Informationen zum Energieverbrauch und Umweltverhalten privater Haushalte bereit. Die Befragung wurde in vier Wellen durchgeführt. Es liegen Daten für die Jahre 2012, 2013, 2014 und 2015 vor. Diese Daten können anhand einer ID aneinander gespielt werden. Darauf aufbauend können ökonometrische Schätzungen und Analysen verschiedener Präferenzindikatoren sowie des Anpassungsverhaltens privater Haushalte an den Klimawandel durchgeführt werden. Dieser Datensatz umfasst die Daten der Erhebung im Jahr 2012. With a share of 30% in total final energy consumption and around 20% in CO2 emissions, private households in Germany strongly affect the environment. At the same time private households are an important target group for policy interventions to fight climate change. Against this background, numerous policy measures that intend to decrease energy consumption and to support renewable energy technologies have been introduced. These policy measures call for accurate evaluation to avoid expensive redundancies due to overlapping policy instruments. The evaluation of energy and environmental policy measures requires comprehensive and reliable data. So far such data was unavailable in Germany, especially in the context of private households. Hence, the responsiveness of German households to climate protection policies was unknown. For this purpose, the Socio-Ecological Panel offers rich information on household’s energy consumption and environmental behavior. The data was gathered in four household surveys conducted in 2012, 2013, 2014 and 2015. The survey waves can be merged using the household ID. The data builds the basis for empirical analyses of households’ adaptation to climate change and the evaluation of environmental and climate policy measures. This data set comprises the information gathered in the 2012 survey wave and is labelled in German. It is available in German and English. Offline Rekrutierung für das repräsentative forsa omninet panel Selbst ausgefüllter Fragebogen Self-completed questionnaire 10.000 deutsche Haushalte Green-SÖP Green-SÖP

Project: Coupled Model Intercomparison Project Phase 6 (CMIP6) datasets - These data have been generated as part of the internationally-coordinated Coupled Model Intercomparison Project Phase 6 (CMIP6; see also GMD Special Issue: http://www.geosci-model-dev.net/special_issue590.html). The simulation data provides a basis for climate research designed to answer fundamental science questions and serves as resource for authors of the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC-AR6). CMIP6 is a project coordinated by the Working Group on Coupled Modelling (WGCM) as part of the World Climate Research Programme (WCRP). Phase 6 builds on previous phases executed under the leadership of the Program for Climate Model Diagnosis and Intercomparison (PCMDI) and relies on the Earth System Grid Federation (ESGF) and the Centre for Environmental Data Analysis (CEDA) along with numerous related activities for implementation. The original data is hosted and partially replicated on a federated collection of data nodes, and most of the data relied on by the IPCC is being archived for long-term preservation at the IPCC Data Distribution Centre (IPCC DDC) hosted by the German Climate Computing Center (DKRZ). The project includes simulations from about 120 global climate models and around 45 institutions and organizations worldwide. Summary: These data include the subset used by IPCC AR6 WGI authors of the datasets originally published in ESGF for 'CMIP6.ScenarioMIP.CSIRO-ARCCSS.ACCESS-CM2.ssp245' with the full Data Reference Syntax following the template 'mip_era.activity_id.institution_id.source_id.experiment_id.member_id.table_id.variable_id.grid_label.version'. The Australian Community Climate and Earth System Simulator Climate Model Version 2 climate model, released in 2019, includes the following components: aerosol: UKCA-GLOMAP-mode, atmos: MetUM-HadGEM3-GA7.1 (N96; 192 x 144 longitude/latitude; 85 levels; top level 85 km), land: CABLE2.5, ocean: ACCESS-OM2 (GFDL-MOM5, tripolar primarily 1deg; 360 x 300 longitude/latitude; 50 levels; top grid cell 0-10 m), seaIce: CICE5.1.2 (same grid as ocean). The model was run by the CSIRO (Commonwealth Scientific and Industrial Research Organisation, Aspendale, Victoria 3195, Australia), ARCCSS (Australian Research Council Centre of Excellence for Climate System Science). Mailing address: CSIRO, c/o Simon J. Marsland, 107-121 Station Street, Aspendale, Victoria 3195, Australia (CSIRO-ARCCSS) in native nominal resolutions: aerosol: 250 km, atmos: 250 km, land: 250 km, ocean: 100 km, seaIce: 100 km.

High-resolution information on climatic conditions is essential to many applications in environmental and ecological sciences. Here we present the CHELSA (Climatologies at high resolution for the earth’s land surface areas) data of downscaled temperature and precipitation to a high resolution of 30 arc sec. The temperature algorithm is based on statistical downscaling of atmospheric temperatures. The precipitation algorithm incorporates orographic predictors including wind fields, valley exposition, and boundary layer height, with a subsequent bias correction. CHELSA data published in EnviDat includes the deprecated version 1.2 (originally published under 10.5061/dryad.kd1d4). Please use the current 2.1 version. Paper Citation: - _Karger DN. et al. Climatologies at high resolution for the earth’s land surface areas, Scientific Data, 4, 170122 (2017) [doi: 10.1038/sdata.2017.122](https://doi.org/10.1038/sdata.2017.122)._

A collection of field data from four agricultural sites in the Rur catchment in Western Germany collected in the frame of the Transregional Collaborative Research Centre 32 “Patterns in Soil-Vegetation-Atmosphere-Systems: Monitoring, Modelling and Data Assimilation” (TR32). The dataset includes data on vegetation (states and fluxes), weather, soil, and agricultural management. Vegetation-related data comprises fresh and dry biomass (green and brown, predominantly per organ), plant height, green and brown leaf area index, phenological development state, nitrogen and carbon content, and carbon-, energy- and water-fluxes for a variety of agricultural plants. In addition, masses of harvest residues and regrowth of vegetation after harvest or before planting of the main crop are included. Data on agricultural management includes sowing and harvest dates, and information on cultivation, fertilization and agrochemicals. The dataset also includes gap-filled weather data and soil parameters (particle size distributions, carbon and nitrogen contents). This data can be useful for development and validation of remote sensing products. A detailed description of the dataset can be found in Reichenau et al. (2020).

Humans share an extraordinary degree of sociality with other primates, calling for comparative work into the evolutionary drivers of the variation in social engagement observed between species. Of particular interest is the contrast between the chimpanzee (Pan troglodytes) and bonobo (Pan paniscus), the latter exhibiting increased female gregariousness, more tolerant relationships, and elaborate behavioral adaptations for conflict resolution. Here we test predictions from three socio-ecological hypotheses regarding the evolution of these traits using data on wild bonobos at LuiKotale, Democratic Republic of Congo. Focusing on the behavior of co-feeding females and controlling for variation in characteristics of the feeding patch, food intake rate moderately increased while feeding effort decreased with female dominance rank, indicating that females engaged in competitive exclusion from high quality food resources. However, these rank effects did not translate into variation in energy balance, as measured from urinary C-peptide levels. Instead, energy balance varied independent of female rank with the proportion of fruit in the diet. Together with the observation that females join forces in conflicts with males, our results support the hypothesis that predicts that females trade off feeding opportunities for safety against male aggression. The key to a full understanding of variation in social structure may be an integrated view of cooperation and competition over access to the key resources food and mates, both within and between the sexes. main_pan_analysis_II_intake_poisson_script_07022017R script for analysing food intake using a GLMMMASTER_analyses_II_R_file_intake_fFile containing the variables for the GLMM on food intake, analysed in RMAIN_pan_analysis_III_movement_script_26092016R script for analysing movement probability in focal trees using GLMMMASTER_analyses_III_R_file_movement_fFile containing the variables to analyse movement probability with a GLMM in Rmain_ucp_model_script_21022018_seasonality_update_with_feedscansR script to analyse variation in urinary C-peptide in a LMMmain_ucp_model_data_r_2018_seasonality_update_with_feed_scansFile containing the variables to analyse variation in urinary C-peptide using an LMM in R

The expansion of irrigated agriculture has increased global crop production but resulted in widespread stress to freshwater resources. Ensuring that increases in irrigated production only occur in places where water is relatively abundant is a key objective of sustainable agriculture, and knowledge of how irrigated land has evolved is important for measuring progress towards water sustainability. Yet a spatially detailed understanding of the evolution of global area equipped for irrigation (AEI) is missing. Here we utilize the latest sub-national irrigation statistics (covering 17298 administrative units) from various official sources to develop a gridded (5 arc-min resolution) global product of AEI for the years 2000, 2005, 2010, and 2015. We find that AEI increased by 11% from 2000 (297 Mha) to 2015 (330 Mha) with locations of both substantial expansion (e.g., northwest India, northeast China) and decline (e.g., Russia). Combining these outputs with information on green (i.e., rainfall) and blue (i.e., surface and ground) water stress, we also examine to what extent irrigation has expanded unsustainably (i.e., in places already experiencing water stress). We find that more than half (52%) of irrigation expansion has taken place in regions that were already water stressed, with India alone accounting for 36% of global unsustainable expansion. These findings provide new insights into the evolving patterns of global irrigation with important implications for global water sustainability and food security. Recommended citation: Mehta, P., Siebert, S., Kummu, M. et al. Half of twenty-first century global irrigation expansion has been in water-stressed regions. Nat Water (2024). https://doi.org/10.1038/s44221-024-00206-9 Open-access peer reviewed publication available at https://www.nature.com/articles/s44221-024-00206-9 Files G_AEI_*.ASC were produced using the GMIA dataset[https://data.apps.fao.org/catalog/iso/f79213a0-88fd-11da-a88f-000d939bc5d8]. Files MEIER_G_AEI_*.ASC were produced using Meier et al. (2018) dataset [https://doi.pangaea.de/10.1594/PANGAEA.884744].