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Microbes play a critical role in plant litter decomposition and influence the fate of carbon in rivers and riparian zones. When decomposing low-nutrient plant litter, microbes acquire nitrogen (N) and phosphorus (P) from the environment (i.e., nutrient immobilization), and this process is potentially sensitive to nutrient loading and changing climate. Nonetheless, environmental controls on immobilization are poorly understood because rates are also influenced by plant litter chemistry, which is coupled to the same environmental factors. Here we used a standardized, low-nutrient organic matter substrate (cotton strips) to quantify nutrient immobilization at 100 paired stream and riparian sites representing 11 biomes worldwide. Immobilization rates varied by three orders of magnitude, were greater in rivers than riparian zones, and were strongly correlated to decomposition rates. In rivers, P immobilization rates were controlled by surface water phosphate concentrations, but N immobilization rates were not related to inorganic N. The N:P of immobilized nutrients was tightly constrained to a molar ratio of 10:1 despite wide variation in surface water N:P. Immobilization rates were temperature-dependent in riparian zones but not related to temperature in rivers. However, in rivers nutrient supply ultimately controlled whether microbes could achieve the maximum expected decomposition rate at a given temperature. Collectively, we demonstrated that exogenous nutrient supply and immobilization are critical control points for decomposition of organic matter. Key Points • Nitrogen (N) and phosphorus (P) immobilization was measured on organic matter (cotton) in 100 rivers and riparian zones representing 11 biomes • Elevated temperature in riparian zones and phosphate in rivers increased immobilization, and consequently accelerated decomposition • N and P immobilization was strongly linked by microbial stoichiometry despite widely varied surface-water nutrient ratios Plain Language Summary Bacteria and fungi contribute to the breakdown of leaf litter in rivers and floodplains. To break down leaf litter, these microbes need the nutrients nitrogen and phosphorus (P), and microbes can get nutrients either from the leaf litter itself or from the environment. Most leaf litter has low nutrient content and microbes must rely on the environment to supply nutrients. We studied microbial nutrient uptake from the environment during litter breakdown to determine whether it varies predictably across the globe and how it is influenced by changing climate and nutrient pollution. In 100 rivers and floodplains in 11 of Earth's major biomes we placed small strips of cotton as stand-ins for leaf litter. Nutrient uptake was consistently greater on cotton strips that were submerged in the river compared to cotton on the floodplain. For microbes in the river, nutrient uptake was faster in instances where there was more P in the water. For microbes in the floodplain, nutrient uptake was faster where temperatures were warmer. Faster nutrient uptake by microbes was linked with faster cotton breakdown in rivers and floodplains. Our study shows that climate change and nutrient pollution can alter the activity of microbes in rivers and floodplains.

Lakes are a dominant feature of the Arctic landscape and a focal point of regional and global biogeochemical cycling. We collected a sediment core from a High Arctic Lake in southwestern Svalbard for multiproxy paleolimnological analysis. The aim was to find linkages between the terrestrial and aquatic environments in the context of climate change to understand centennial-long Arctic biogeochemical cycling and environmental dynamics. Two significant thresholds in elemental cycling were found based on sediment physical and biogeochemical proxies that were associated with the end of the cold Little Ice Age and the recent warming. We found major shifts in diatom, chironomid and cladoceran communities and their functionality that coincided with increased summer temperatures since the 1950s. We also discovered paleoecological evidence that point toward expanded bird (Little Auk) colonies in the catchment alongside climate warming. Apparently, climate-driven increase in glacier melt water delivery as well as a prolonged snow- and ice-free period have increased the transport of mineral matter from the catchment, causing significant water turbidity and disappearance of several planktonic diatoms and clear-water chironomids. We also found sedimentary accumulation of microplastic particles following the increase in Little Auk populations suggesting that seabirds potentially act as biovectors for plastic contamination. Our study demonstrates the diverse nature of climate-driven changes in the Arctic lacustrine environment with increased inorganic input from the more exposed catchment, larger nutrient delivery from the increased bird colonies at the surrounding mountain summits and subsequent alterations in aquatic communities.

International audience; The quantification of sources and sinks of carbon from land use and land cover changes (LULCC) is uncertain. We investigated how the parametrization of LULCC and of organic matter decomposition, as well as initial land cover, affects the historical and future carbon fluxes in an Earth System Model (ESM). Using the land component of the Max Planck Institute ESM, we found that the historical (1750-2010) LULCC flux varied up to 25% depending on the fraction of biomass which enters the atmosphere directly due to burning or is used in short-lived products. The uncertainty in the decadal LULCC fluxes of the recent past due to the parametrization of decomposition and direct emissions was 0.6 Pg C yr −1 , which is 3 times larger than the uncertainty previously attributed to model and method in general. Preindustrial natural land cover had a larger effect on decadal LULCC fluxes than the aforementioned parameter sensitivity (1.0 Pg C yr −1). Regional differences between reconstructed and dynamically computed land covers, in particular, at low latitudes, led to differences in historical LULCC emissions of 84-114 Pg C, globally. This effect is larger than the effects of forest regrowth, shifting cultivation, or climate feedbacks and comparable to the effect of differences among studies in the terminology of LULCC. In general, we find that the practice of calibrating the net land carbon balance to provide realistic boundary conditions for the climate component of an ESM hampers the applicability of the land component outside its primary field of application.

Considering the combined effects of CO2 fertilization and climate change drivers on plant physiology leads to a modest increase in simulated European forest transpiration in spite of the effects of CO2-induced stomatal closure. The Earth’s carbon and hydrologic cycles are intimately coupled by gas exchange through plant stomata1,2,3. However, uncertainties in the magnitude4,5,6 and consequences7,8 of the physiological responses9,10 of plants to elevated CO2 in natural environments hinders modelling of terrestrial water cycling and carbon storage11. Here we use annually resolved long-term δ13C tree-ring measurements across a European forest network to reconstruct the physiologically driven response of intercellular CO2 (Ci) caused by atmospheric CO2 (Ca) trends. When removing meteorological signals from the δ13C measurements, we find that trees across Europe regulated gas exchange so that for one ppmv atmospheric CO2 increase, Ci increased by ∼0.76 ppmv, most consistent with moderate control towards a constant Ci/Ca ratio. This response corresponds to twentieth-century intrinsic water-use efficiency (iWUE) increases of 14 ± 10 and 22 ± 6% at broadleaf and coniferous sites, respectively. An ensemble of process-based global vegetation models shows similar CO2 effects on iWUE trends. Yet, when operating these models with climate drivers reintroduced, despite decreased stomatal opening, 5% increases in European forest transpiration are calculated over the twentieth century. This counterintuitive result arises from lengthened growing seasons, enhanced evaporative demand in a warming climate, and increased leaf area, which together oppose effects of CO2-induced stomatal closure. Our study questions changes to the hydrological cycle, such as reductions in transpiration and air humidity, hypothesized to result from plant responses to anthropogenic emissions.