The HydroATLAS database provides a standardized compendium of descriptive hydro-environmental information for all watersheds and rivers of the world at high spatial resolution. Version 1.0 of HydroATLAS offers data for 56 variables, partitioned into 281 individual attributes and organized in six categories: hydrology; physiography; climate; land cover & use; soils & geology; and anthropogenic influences. HydroATLAS derives the hydro-environmental characteristics by aggregating and reformatting original data from well-established global digital maps, and by accumulating them along the drainage network from headwaters to ocean outlets. The attributes are linked to hierarchically nested sub-basins at multiple scales, as well as to individual river reaches, both extracted from the global HydroSHEDS database at 15 arc-second (~500 m) resolution. The sub-basin and river reach information is offered in two companion datasets: BasinATLAS and RiverATLAS. The standardized format of HydroATLAS ensures easy applicability while the inherent topological information supports basic network functionality such as identifying up- and downstream connections. HydroATLAS is fully compatible with other products of the overarching HydroSHEDS project enabling versatile hydro-ecological assessments for a broad user community.

The thermal-based two-source energy balance (TSEB) model has accurately simulated energy fluxes in a wide range of landscapes with both remote and proximal sensing data. However, tree-grass ecosystems (TGE) have notably complex heterogeneous vegetation mixtures and dynamic phenological characteristics presenting clear challenges to earth observation and modeling methods. Particularly, the TSEB modeling structure assumes a single vegetation source, making it difficult to represent the multiple vegetation layers present in TGEs (i.e., trees and grasses) which have different phenological and structural characteristics. This study evaluates the implementation of TSEB in a TGE located in central Spain and proposes a new strategy to consider the spatial and temporal complexities observed. This was based on sensitivity analyses (SA) conducted on both primary remote sensing inputs (local SA) and model parameters (global SA). The model was subsequently modified considering phenological dynamics in semi-arid TGEs and assuming a dominant vegetation structure and cover (i.e., either grassland or broadleaved trees) for different seasons (TSEB-2S). The adaptation was compared against the default model and evaluated against eddy covariance (EC) flux measurements and lysimeters over the experimental site. TSEB-2S vastly improved over the default TSEB performance decreasing the mean bias and root-mean-square-deviation (RMSD) of latent heat (LE) from 40 and 82 W m−2 to −4 and 59 W m−2, respectively during 2015. TSEB-2S was further validated for two other EC towers and for different years (2015, 2016 and 2017) obtaining similar error statistics with RMSD of LE ranging between 57 and 63 W m−2. The results presented here demonstrate a relatively simple strategy to improve water and energy flux monitoring over a complex and vulnerable landscape, which are often poorly represented through remote sensing models.

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It is well documented that energy balance and other remote sensing‐based evapotranspiration (ET) models face greater uncertainty over water‐limited tree‐grass ecosystems (TGEs), representing nearly 1/6th of the global land surface. Their dual vegetation strata, the grass‐dominated understory and tree‐dominated overstory, make for distinct structural, physiological and phenological characteristics, which challenge models compared to more homogeneous and energy‐limited ecosystems. Along with this, the contribution of grasses and trees to total transpiration (T), along with their different climatic drivers, is still largely unknown nor quantified in TGEs. This study proposes a thermal‐based three‐source energy balance (3SEB) model, accommodating an additional vegetation source within the well‐known two‐source energy balance (TSEB) model. The model was implemented at both tower and continental scales using eddy‐covariance (EC) TGE sites, with variable tree canopy cover and rainfall (P) regimes and Meteosat Second Generation (MSG) images. 3SEB robustly simulated latent heat (LE) and related energy fluxes in all sites (Tower: LE RMSD ~60 W/m2; MSG: LE RMSD ~90 W/m2), improving over both TSEB and seasonally changing TSEB (TSEB‐2S) models. In addition, 3SEB inherently partitions water fluxes between the tree, grass and soil sources. The modelled T correlated well with EC T estimates (r > .76), derived from a machine learning ET partitioning method. The T/ET was found positively related to both P and leaf area index, especially compared to the decomposed grass understory T/ET. However, trees and grasses had contrasting relations with respect to monthly P. These results demonstrate the importance in decomposing total ET into the different vegetation sources, as they have distinct climatic drivers, and hence, different relations to seasonal water availability. These promising results improved ET and energy flux estimations over complex TGEs, which may contribute to enhance global drought monitoring and understanding, and their responses to climate change feedbacks.

Nutrient availability, especially of nitrogen (N) and phosphorus (P), is of major importance for every organism and at a larger scale for ecosystem functioning and productivity. Changes in nutrient availability and potential stoichiometric imbalance due to anthropogenic nitrogen deposition might lead to nutrient deficiency or alter ecosystem functioning in various ways. In this study, we present 6 years (2014–2020) of flux‐, plant‐, and remote sensing data from a large‐scale nutrient manipulation experiment conducted in a Mediterranean savanna‐type ecosystem with an emphasis on the effects of N and P treatments on ecosystem‐scale water‐use efficiency (WUE) and related mechanisms. Two plots were fertilized with N (NT, 16.9 Ha) and N + P (NPT, 21.5 Ha), and a third unfertilized plot served as a control (CT). Fertilization had a strong impact on leaf nutrient stoichiometry only within the herbaceous layer with increased leaf N in both fertilized treatments and increased leaf P in NPT. Following fertilization, WUE in NT and NPT increased during the peak of growing season. While gross primary productivity similarly increased in NT and NPT, transpiration and surface conductance increased more in NT than in NPT. The results show that the NPT plot with higher nutrient availability, but more balanced N:P leaf stoichiometry had the highest WUE. On average, higher N availability resulted in a 40% increased leaf area index (LAI) in both fertilized treatments in the spring. Increased LAI reduced aerodynamic conductance and thus evaporation at both fertilized plots in the spring. Despite reduced evaporation, annual evapotranspiration increased by 10% (48.6 ± 28.3 kg H2O m−2), in the NT plot, while NPT remained similar to CT (−1%, −6.7 ± 12.2 kgH2O m−2). Potential causes for increased transpiration at NT could be increased root biomass and thus higher water uptake or rhizosphere priming to increase P‐mobilization through microbes. The annual net ecosystem exchange shifted from a carbon source in CT (75.0 ± 20.6 gC m−2) to carbon‐neutral in both fertilized treatments [−7.0 ± 18.5 gC m−2 (NT) 0.4 ± 22.6 gC m−2 (NPT)]. Our results show, that the N:P stoichiometric imbalance, resulting from N addition (without P), increases the WUE less than the addition of N + P, due to the strong increase in transpiration at NT, which indicates the importance of a balanced N and P content for WUE.