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Abstract Global warming increases ecosystem respiration (ER), creating a positive carbon-climate feedback. Thermal acclimation, the direct responses of biological communities to reduce the effects of temperature changes on respiration rates, is a critical mechanism that compensates for warming-induced ER increases and dampens this positive feedback. However, the extent and effects of this mechanism across diverse ecosystems remain unclear. By analyzing CO2 flux data from 93 eddy covariance sites worldwide, we observed thermal acclimation at 84 % of the sites. If sustained, thermal acclimation could reduce projected warming-induced nighttime ER increases by at least 25 % across most climate zones by 2041-2060. Strong thermal acclimation is particularly evident in ecosystems at high elevation, with low-carbon-content soils, and within tundra, semi-arid, and warm-summer Mediterranean climates, supporting the hypothesis that extreme environments favor the evolution of greater acclimation potential. Moreover, ecosystems with dense vegetation and high productivity such as humid tropical and subtropical forests generally exhibit strong thermal acclimation, suggesting that regions with substantial CO2 uptake may continue to serve as strong carbon sinks. Conversely, some ecosystems in cold continental climates show signs of enhancing thermal responses, the opposite of thermal acclimation, which could exacerbate carbon losses as climate warms. Our study underscores the widespread yet climate-specific patterns of thermal acclimation in global terrestrial ER, emphasizing the need to incorporate these patterns into Earth System Models for more accurate carbon-climate feedback projections. 

Abstract We examined the seasonality of photosynthesis in 46 evergreen needleleaf (evergreen needleleaf forests (ENF)) and deciduous broadleaf (deciduous broadleaf forests (DBF)) forests across North America and Eurasia. We quantified the onset and end (Start_GPPand End_GPP) of photosynthesis in spring and autumn based on the response of net ecosystem exchange of CO₂to sunlight. To test the hypothesis that snowmelt is required for photosynthesis to begin, these were compared with end of snowmelt derived from soil temperature. ENF forests achieved 10% of summer photosynthetic capacity ∼3 weeks before end of snowmelt, while DBF forests achieved that capacity ∼4 weeks afterward. DBF forests increased photosynthetic capacity in spring faster (1.95% d⁻¹) than ENF (1.10% d⁻¹), and their active season length (End_GPP–Start_GPP) was ∼50 days shorter. We hypothesized that warming has influenced timing of the photosynthesis season. We found minimal evidence for long‐term change in Start_GPP, End_GPP, or air temperature, but their interannual anomalies were significantly correlated. Warmer weather was associated with earlier Start_GPP(1.3–2.5 days °C⁻¹) or later End_GPP(1.5–1.8 days °C⁻¹, depending on forest type and month). Finally, we tested whether existing phenological models could predict Start_GPPand End_GPP. For ENF forests, air temperature‐ and daylength‐based models provided best predictions for Start_GPP, while a chilling‐degree‐day model was best for End_GPP. The root mean square errors (RMSE) between predicted and observed Start_GPPand End_GPPwere 11.7 and 11.3 days, respectively. For DBF forests, temperature‐ and daylength‐based models yielded the best results (RMSE 6.3 and 10.5 days). 

Abstract Fundamental axes of variation in plant traits result from trade-offs between costs and benefits of resource-use strategies at the leaf scale. However, it is unclear whether similar trade-offs propagate to the ecosystem level. Here, we test whether trait correlation patterns predicted by three well-known leaf- and plant-level coordination theories – the leaf economics spectrum, the global spectrum of plant form and function, and the least-cost hypothesis – are also observed between community mean traits and ecosystem processes. We combined ecosystem functional properties from FLUXNET sites, vegetation properties, and community mean plant traits into three corresponding principal component analyses. We find that the leaf economics spectrum (90 sites), the global spectrum of plant form and function (89 sites), and the least-cost hypothesis (82 sites) all propagate at the ecosystem level. However, we also find evidence of additional scale-emergent properties. Evaluating the coordination of ecosystem functional properties may aid the development of more realistic global dynamic vegetation models with critical empirical data, reducing the uncertainty of climate change projections. 

Abstract In eddy covariance measurements, the storage flux represents the variation in time of the dry molar fraction of a given gas in the control volume representative of turbulent flux. Depending on the time scale considered, and on the height above ground of the measurements, it can either be a major component of the overall net ecosystem exchange or nearly negligible. Instrumental configuration and computational procedures must be optimized to measure this change at the time step used for the turbulent flux measurement. Three different configurations are suitable within the Integrated Carbon Observation System infrastructure for the storage flux determination: separate sampling, subsequent sampling and mixed sampling. These configurations have their own advantages and disadvantages, and must be carefully selected based on the specific features of the considered station. In this paper, guidelines about number and distribution of vertical and horizontal sampling points are given. Details about suitable instruments, sampling devices, and computational procedures for the quantification of the storage flux of different GHG gases are also provided. 

Abstract. Mapping in situ eddy covariance measurements of terrestrial land–atmosphere fluxes to the globe is a key method for diagnosing the Earth system from a data-driven perspective. We describe the first global products (called X-BASE) from a newly implemented upscaling framework, FLUXCOM-X, representing an advancement from the previous generation of FLUXCOM products in terms of flexibility and technical capabilities. The X-BASE products are comprised of estimates of CO2 net ecosystem exchange (NEE), gross primary productivity (GPP), evapotranspiration (ET), and for the first time a novel, fully data-driven global transpiration product (ETT), at high spatial (0.05°) and temporal (hourly) resolution. X-BASE estimates the global NEE at −5.75 ± 0.33 Pg C yr−1 for the period 2001–2020, showing a much higher consistency with independent atmospheric carbon cycle constraints compared to the previous versions of FLUXCOM. The improvement of global NEE was likely only possible thanks to the international effort to increase the precision and consistency of eddy covariance collection and processing pipelines, as well as to the extension of the measurements to more site years resulting in a wider coverage of bioclimatic conditions. However, X-BASE global net ecosystem exchange shows a very low interannual variability, which is common to state-of-the-art data-driven flux products and remains a scientific challenge. With 125 ± 2.1 Pg C yr−1 for the same period, X-BASE GPP is slightly higher than previous FLUXCOM estimates, mostly in temperate and boreal areas. X-BASE evapotranspiration amounts to 74.7×103 ± 0.9×103 km3 globally for the years 2001–2020 but exceeds precipitation in many dry areas, likely indicating overestimation in these regions. On average 57 % of evapotranspiration is estimated to be transpiration, in good agreement with isotope-based approaches, but higher than estimates from many land surface models. Despite considerable improvements to the previous upscaling products, many further opportunities for development exist. Pathways of exploration include methodological choices in the selection and processing of eddy covariance and satellite observations, their ingestion into the framework, and the configuration of machine learning methods. For this, the new FLUXCOM-X framework was specifically designed to have the necessary flexibility to experiment, diagnose, and converge to more accurate global flux estimates. 

Abstract The eddy covariance is a powerful technique to estimate the surface-atmosphere exchange of different scalars at the ecosystem scale. The EC method is central to the ecosystem component of the Integrated Carbon Observation System, a monitoring network for greenhouse gases across the European Continent. The data processing sequence applied to the collected raw data is complex, and multiple robust options for the different steps are often available. For Integrated Carbon Observation System and similar networks, the standardisation of methods is essential to avoid methodological biases and improve comparability of the results. We introduce here the steps of the processing chain applied to the eddy covariance data of Integrated Carbon Observation System stations for the estimation of final CO 2 , water and energy fluxes, including the calculation of their uncertainties. The selected methods are discussed against valid alternative options in terms of suitability and respective drawbacks and advantages. The main challenge is to warrant standardised processing for all stations in spite of the large differences in e.g . ecosystem traits and site conditions. The main achievement of the Integrated Carbon Observation System eddy covariance data processing is making CO 2 and energy flux results as comparable and reliable as possible, given the current micrometeorological understanding and the generally accepted state-of-the-art processing methods. 

Abstract The Integrated Carbon Observation System Research Infrastructure aims to provide long-term, continuous observations of sources and sinks of greenhouse gases such as carbon dioxide, methane, nitrous oxide, and water vapour. At ICOS ecosystem stations, the principal technique for measurements of ecosystem-atmosphere exchange of GHGs is the eddy-covariance technique. The establishment and setup of an eddy-covariance tower have to be carefully reasoned to ensure high quality flux measurements being representative of the investigated ecosystem and comparable to measurements at other stations. To fulfill the requirements needed for flux determination with the eddy-covariance technique, variations in GHG concentrations have to be measured at high frequency, simultaneously with the wind velocity, in order to fully capture turbulent fluctuations. This requires the use of high-frequency gas analysers and ultrasonic anemometers. In addition, to analyse flux data with respect to environmental conditions but also to enable corrections in the post-processing procedures, it is necessary to measure additional abiotic variables in close vicinity to the flux measurements. Here we describe the standards the ICOS ecosystem station network has adopted for GHG flux measurements with respect to the setup of instrumentation on towers to maximize measurement precision and accuracy while allowing for flexibility in order to observe specific ecosystem features. 

Abstract The leaf economics spectrum 1,2 and the global spectrum of plant forms and functions 3 revealed fundamental axes of variation in plant traits, which represent different ecological strategies that are shaped by the evolutionary development of plant species 2 . Ecosystem functions depend on environmental conditions and the traits of species that comprise the ecological communities 4 . However, the axes of variation of ecosystem functions are largely unknown, which limits our understanding of how ecosystems respond as a whole to anthropogenic drivers, climate and environmental variability 4,5 . Here we derive a set of ecosystem functions 6 from a dataset of surface gas exchange measurements across major terrestrial biomes. We find that most of the variability within ecosystem functions (71.8%) is captured by three key axes. The first axis reflects maximum ecosystem productivity and is mostly explained by vegetation structure. The second axis reflects ecosystem water-use strategies and is jointly explained by variation in vegetation height and climate. The third axis, which represents ecosystem carbon-use efficiency, features a gradient related to aridity, and is explained primarily by variation in vegetation structure. We show that two state-of-the-art land surface models reproduce the first and most important axis of ecosystem functions. However, the models tend to simulate more strongly correlated functions than those observed, which limits their ability to accurately predict the full range of responses to environmental changes in carbon, water and energy cycling in terrestrial ecosystems 7,8 .