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The data consists of annual measurements of standing aboveground plant biomass, annual aboveground net primary productivity and annual soil respiration between 1998 and 2012. Data were collected from seven European shrublands that were subject to the climate manipulations drought and warming. Sites were located in the United Kingdom (UK), the Netherlands (NL), Denmark ( two sites, DK-B and DK-M), Hungary (HU), Spain (SP) and Italy (IT). All field sites consisted of untreated control plots, plots where the plant canopy air is artificially warmed during night time hours, and plots where rainfall is excluded from the plots at least during the plants growing season. Standing aboveground plant biomass (grams biomass per square metre) was measured in two undisturbed areas within the plots using the pin-point method (UK, DK-M, DK-B), or along a transect (IT, SP, HU, NL). Aboveground net primary productivity was calculated from measurements of standing aboveground plant biomass estimates and litterfall measurements. Soil respiration was measured in pre-installed opaque soil collars bi-weekly, monthly, or in measurement campaigns (SP only). The datasets provided are the basis for the data analysis presented in Reinsch et al. (2017) Shrubland primary production and soil respiration diverge along European climate gradient. Scientific Reports 7:43952 https://doi.org/10.1038/srep43952 Standing biomass was measured using the non-destructive pin-point method to assess aboveground biomass. Measurements were conducted at the state of peak biomass specific for each site. Litterfall was measured annually using litterfall traps. Litter collected in the traps was dried and the weight was measured. Aboveground biomass productivity was estimated as the difference between the measured standing biomass in year x minus the standing biomass measured the previous year. Soil respiration was measured bi-weekly or monthly, or in campaigns (Spain only). It was measured on permanently installed soil collars in treatment plots. The Gaussen Index of Aridity (an index that combines information on rainfall and temperature) was calculated using mean annual precipitation, mean annual temperature. The reduction in precipitation and increase in temperature for each site was used to calculate the Gaussen Index for the climate treatments for each site. Data of standing biomass and soil respiration was provided by the site responsible. Data from all sites were collated into one data file for data analysis. A summary data set was combined with information on the Gaussen Index of Aridity Data were then exported from these Excel spreadsheet to .csv files for ingestion into the EIDC.

Figure 1data_Exp 2Figure 1 data: Condition of experimental seedlings in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS) during the warmest growing season (2011) and at the end of the experiment (2013). Seedling condition was defined as: healthy (< 50% of the needles turned yellow or brown) or unhealthy (> 50% of the needles turned yellow or brown). Seedlings were 1 month old at plantation time in the July 2010.Table 1_environmental conditions_Exp 1Table 1 data: Environmental conditions and vegetation characteristics in hummocks (circular and bands) and lawns for Experiment 1. Water table depth below surface is an average for the four growing seasons (2010-2013)Table 2_ photosynthesis data_Exp 1Table 2 photosynthesis data: Photosynthesis rates for experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns for Experiment 1.Table 2_seedling responses_Exp 1Table 2 data: Responses of experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns for Experiment 1 after 4 growing seasons. ST: Seeds inserted on top of moss; SB: Seeds inserted below moss; Small seedling (1 month old at plantation time); Large seedling (2 months old at plantation time). Emergence = % of planted seeds emerged after 1 year. Condition = % healthy seedlings. Stem growth corresponds to vertical stem growth for germinating (ST and SB) seedlings and new stem growth for older (small and large) seedlings.Table 3_regression seedling-environment_Exp 1Table 3 data for generalized linear models assessing the responses of experimental pine seedlings in hummocks (circular and bands) and adjacent lawns for Experiment 1 during the whole experimental period (2010-2013). ST: Seedlings from seeds inserted on top of moss; SB: Seedlings from seeds inserted below moss; Small seedling (1 month old at plantation time); Large seedling (2 months old at plantation time). Condition = % healthy seedlings. Growth = stem growth.Table 4_Environmental data_Exp 2Table 4: Environmental conditions in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS).Table 4 and Table S5a_seedling performance_Exp 2Table 4: Seedling performance in hummocks with contrasting shrub density and tree canopy in Experiment 2: No Trees - Low Shrub biomass (NTLS), No Trees - High Shrub biomass (NTHS), Present Trees - Low Shrub biomass (PTLS) and Present Trees - High shrub biomass (PTHS). Seedling emergence, condition and survival from seeds inserted below the moss (SB), and from small planted seedlings.Table S3_cox regression (survival analysis)_Exp 1Table S3: Data for Cox survival analysis for experimental pine seedlings in hummocks (circular and bands) versus adjacent lawns during 2010-2013. ST: Seedlings from seeds inserted on top of moss; SB: Seedlings from seeds inserted below moss; Small seedling (1 month old, 10 cm tall at plantation time); Large seedling (2 months old, 30 cm tall at plantation time).Table S4_ regression seedling-environment 2011_Exp 1Table S4: Data for generalized linear models assessing the responses of experimental pine seedlings in hummocks (circular and bands) and adjacent lawns for Experiment 1 in 2011. Small seedling (1 month old, 10 cm tall at plantation time); Large seedling (2 months old, 30 cm tall at plantation time). Condition = % healthy seedlings. Growth = stem growth. Boreal ecosystems are warming roughly twice as fast as the global average, resulting in woody expansion that could further speed up the climate warming. Boreal peatbogs are waterlogged systems that store more than 30% of the global soil carbon. Facilitative effects of shrubs and trees on the establishment of new individuals could increase tree cover with profound consequences for the structure and functioning of boreal peatbogs, carbon sequestration and climate. We conducted two field experiments in boreal peatbogs to assess the mechanisms that explain tree seedling recruitment and to estimate the strength of positive feedbacks between shrubs and trees. We planted seeds and seedlings of Pinus sylvestris in microsites with contrasting water-tables and woody cover and manipulated both shrub canopy and root competition. We monitored seedling emergence, growth and survival for up to four growing seasons and assessed how seedling responses related to abiotic and biotic conditions. We found that tree recruitment is more successful in drier topographical microsites with deeper water-tables. On these hummocks, shrubs have both positive and negative effects on tree seedling establishment. Shrub cover improved tree seedling condition, growth and survival during the warmest growing season. In turn, higher tree basal area correlates positively with soil nutrient availability, shrub biomass and abundance of tree juveniles. Synthesis. Our results suggest that shrubs facilitate tree colonization of peatbogs which further increases shrub growth. These facilitative effects seem to be stronger under warmer conditions suggesting that a higher frequency of warmer and dry summers may lead to stronger positive interactions between shrubs and trees that could eventually facilitate a shift from moss to tree-dominated systems.

In the agricultural sector, climate change (CC) affects multiple weather variables at different stages of crop cycles. CC may influence the mean level or affect the distribution of events (e.g., rainfall, temperature). This work evaluates the economic impact of CC-related changes in multiple climatic components, and the resulting uncertainty. For this purpose, a three-stage discrete stochastic programming model is used to represents farm sector of an irrigated area of Italy and to examine the influence of CC on rainfall and on maximum temperature. These variables affect the availability of water for agriculture and the water requirements of irrigated crops. The states of nature, and their change, are defined more broadly than in previous analyses; this allows examining the changes of more climatic variables and crops cultivation. The effect of CC is obtained by comparing the results of scenarios that represent the climatic conditions in the current situation and in the future. The results show that the agricultural sector would seek to lower costs by modifying patterns of land use, farming practices and increasing the use groundwater. The overall economic impact of these changes is small and due primarily to the reduced availability of water in the future. The temperature increase is, in fact, largely offset by the effects of the increase in CO2 levels, which boosts the yield of main crops of the irrigated zone. Therefore, availability and water management becomes a crucial factor to offset the increase of evapotranspiration and of water stress resulting from the increase of temperature. However, the costs of CC are very high for some types of farming, which suffer a large reduction in income.

Energy Climate dataset consistent with ENTSO-E Pan-European Climatic Database (PECD 2021.3) in CSV and netCDF format TL;DR: this is a nationally aggregated hourly dataset for the capacity factors per unit installed capacity for storage hydropower plants and run-of-river hydropower plants in the European region. All the data is provided for 30 climatic years (1981-2010). Method Description The hydro inflow data is based on historical river runoff reanalysis data simulated by the E-HYPE model. E-HYPE is a pan-European model developed by The Swedish Meteorological and Hydrological Institute (SMHI), which describes hydrological processes including flow paths at the subbasin level. E-hype only provides the time series of daily river runoff entering the inlet of each European subbasin over 1981-2010. To match the operational resolution of the dispatch model, we linearly downscale these time series to hourly. By summing up runoff associated with the inlet subbasins of each country, we also obtain the country-level river runoff. The hydro inflow time series per country is defined as the normalized energy inflows (per unit installed capacity of hydropower) embodied in the country-level river runoff. A dispatch model can be used to decides whether the energy inflows are actually used for electricity generation, stored, or spilled (in case the storage reservoir is already full). Data coverage This dataset considers two types of hydropower plants, namely storage hydropower plant (STO) and run-of-river hydropower plant (ROR). Not all countries have both types of hydropower plants installed (see table). The countries and their acronyms for both technologies included in this dataset are: Country Run-of-River Storage Austria AT_ROR AT_STO Belgium BE_ROR BE_STO Bulgaria BG_ROR BG_STO Switzerland CH_ROR CH_STO Cyprus CZ_ROR CZ_STO Germany DE_ROR DE_STO Denmark DK_ROR Estonia EE_ROR Greece EL_ROR EL_STO Spain ES_ROR ES_STO Finland FI_ROR FI_STO France FR_ROR FR_STO Great Britain GB_ROR GB_STO Croatia HR_ROR HR_STO Hungary HU_ROR HU_STO Ireland IE_ROR IE_STO Italy IT_ROR IT_STO Luxembourg LU_ROR Latvia LV_ROR the Netherlands NL_ROR Norway NO_ROR NO_STO Poland PL_ROR PL_STO Portugal PT_ROR PT_STO Romania RO_ROR RO_STO Sweden SE_ROR SE_STO Slovenia SI_ROR SI_STO Slovakia SK_ROR SK_STO Data structure description The files is provided in CSV (.csv) format with a comma (,) as separator and double-quote mark (") as text indicator. The first row stores the column labels. The columns contain the following: first column (or A) contains the row number Label: unlabeled Contents: interger range [1,262968] second column (or B) contains the valid-time Label: T1h Contents represent time with text as [DD/MM/YYYY HH:MM]) column 3-52 (or C-AY) each contain the capacity factor for each valid combination of a country and hydropower plant type Label: XX_YYY the two letter country code (XX) and the hydropower plant type (YYY) acronym for storage hydropower plant (STO) and run-of-river hydropower plant (ROR) Contents represent the capacity factor as a floating value in the range [0,1], the decimal separator is a point (.). DISCLAIMER: the content of this dataset has been created with the greatest possible care. However, we invite to use the original data for critical applications and studies. The raw hydro data was generated as part of 'Evaluating sediment Delivery Impacts on Reservoirs in changing climaTe and society across scales and sectors (DIRT-X)', this project and therefor, Jing hu, received funding from the European Research Area Network (ERA-NET) under grant number 438.19.902. Laurens P. Stoop received funding from the Netherlands Organization for Scientific Research (NWO) under Grant No. 647.003.005.

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.

Water resources index W quantifies the potential dependence of the world's lowland areas on water resources originating in mountain areas upstream. The data cover the timeframe from the 1960s (1961–1970) to the 2040s (2041–2050) in decadal steps. Data for projections from the 2010s onwards are available for three scenario pathways (SSP1-RCP4.5, SSP2-RCP6.0, SSP3-RCP6.0) and show median results from 5 CMIP5 GCMs (GFDL-ESM2M, HadGEM2-ES, IPSL-CM5A-LR, MIROC-ESM-CHEM, NorESM1‑M). The files are GeoTIFF formatted and in a regular raster of 5’×5’ (arc minutes in WGS 1984 coordinate system) The values of W can be classified using the following ranges: W ≤ -2 → Essential but vastly insufficient -2 < W < -1 → Essential but insufficient -1 ≤ W < 0 → Essential and sufficient W = 0 → No surplus from mountains 0 < W ≤ 1 → Supportive 1 < W < 2 → Minor W ≥ 2 → Negligible The values of W are rounded to four decimal places and limited to a range of -1110 to 9998. Values falling outside of that range are set to the nearest limit. he following flag values apply to W: -5555 indicates that there is no water balance surplus from the mountain area upstream, but a lowland water balance surplus; -6666 indicates that there is no water balance surplus from the mountain area upstream, and a lowland water balance deficit. Mountain areas and oceans are NODATA, large ice shields are omitted (Greenland: NODATA, Antarctica: not covered in extent). Mountain areas provide disproportionally high runoff in many parts of the world, and here we quantify for the first time their importance for water resources and food production from the viewpoint of the lowland areas downstream. The dataset maps the degree to which lowland areas potentially depend on runoff contributions from mountain areas (39% of land mass) between the 1960s and the 2040s.

Projections of Sea Level Rise (SLR) under RCP 4.5 and RCP 8.5 (AR5) along the Mekong Coast, Published1 by the Ministry of Natural Resources and Environment (MONRE), Hanoi, Vietnam. Projections of Mekong River discharge during the dry season under RCP 4.5 and RCP 8.5 at Kratie, Cambodia. The data contains the cumulative, minimum and maximum dry season (January-1st to April-30th) discharge from 5 different climate models. PCR-GLOBWB2 was run at 5 arc-min spatial resolution and forced with the data based on output from five ISIMIP CMIP5 global climate models (HadGEM2-ES, GFDL-ESM2, IPSL-CM5A-LR, MIROC-ESM-CHEM, NorESM1-M). 1. Ministry of Natural Resources and Environment (MONRE), V. Climate change and sea level rise scenarios for Vietnam, Ministry of Natural Resources and Environment. (2016). 2. Sutanudjaja, E. H. et al. PCR-GLOBWB 2: a 5 arcmin global hydrological and water resources model. Geosci. Model Dev. 11, 2429–2453 (2018). {"references": ["Sutanudjaja et al. (2018)", "Ministry of Natural Resources and Environment (2016)"]}

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].