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Stable isotope ratios of H (δ²H), O (δ¹⁸O), and C (δ¹³C) are linked to key biogeochemical processes of the water and carbon cycles; however, the degree to which isotope-associated processes are reflected in macroscale ecosystem flux observations remains unquantified. Here through formal information assessment, new measurements ofδ¹³C of net ecosystem exchange (NEE) as well asδ²H andδ¹⁸O of latent heat (LH) fluxes across the United States National Ecological Observation Network (NEON) are used to determine conditions under which isotope measurements are informative of environmental exchanges. We find all three isotopic datasets individually contain comparable amounts of information aboutNEEandLHfluxes as wind speed observations. Such information from isotope measurements, however, is largely unique. Generally,δ¹³C provides more information aboutLHas aridity increases or mean annual precipitation decreases.δ²H provides more information aboutLHas temperatures or mean annual precipitation decreases, and also provides more information aboutNEEas temperatures decrease. Overall, we show that the stable isotope datasets collected by NEON contribute non-trivial amounts of new information about bulk environmental fluxes useful for interpreting biogeochemical and ecohydrological processes at landscape scales. However, the utility of this new information varies with environmental conditions at continental scales. This study provides an approach for quantifying the value adding non-traditional sensing approaches to environmental monitoring sites and the patterns identified here are expected to aid in modeling and data interpretation efforts focused on constraining carbon and water cycles’ mechanisms.

 

The National Ecological Observatory Network (NEON) provides open-access measurements of stable isotope ratios in atmospheric water vapor (δ²H, δ¹⁸O) and carbon dioxide (δ¹³C) at different tower heights, as well as aggregated biweekly precipitation samples (δ²H, δ¹⁸O) across the United States. These measurements were used to create the NEON Daily Isotopic Composition of Environmental Exchanges (NEON-DICEE) dataset estimating precipitation (P; δ²H, δ¹⁸O), evapotranspiration (ET; δ²H, δ¹⁸O), and net ecosystem exchange (NEE; δ¹³C) isotope ratios. Statistically downscaled precipitation datasets were generated to be consistent with the estimated covariance between isotope ratios and precipitation amounts at daily time scales. Isotope ratios in ET and NEE fluxes were estimated using a mixing-model approach with calibrated NEON tower measurements. NEON-DICEE is publicly available on HydroShare and can be reproduced or modified to fit user specific applications or include additional NEON data records as they become available. The NEON-DICEE dataset can facilitate understanding of terrestrial ecosystem processes through their incorporation into environmental investigations that require daily δ²H, δ¹⁸O, and δ¹³C flux data.

 

Abstract Sampling intervals of precipitation geochemistry measurements are often coarser than those required by fine-scale hydrometeorological models. This study presents a statistical method to temporally downscale geochemical tracer signals in precipitation so that they can be used in high-resolution, tracer-enabled applications. In this method, we separated the deterministic component of the time series and the remaining daily stochastic component, which was approximated by a conditional multivariate Gaussian distribution. Specifically, statistics of the stochastic component could be explained from coarser data using a newly identified power-law decay function, which relates data aggregation intervals to changes in tracer concentration variance and correlations with precipitation amounts. These statistics were used within a copula framework to generate synthetic tracer values from the deterministic and stochastic time series components based on daily precipitation amounts. The method was evaluated at 27 sites located worldwide using daily precipitation isotope ratios, which were aggregated in time to provide low resolution testing datasets with known daily values. At each site, the downscaling method was applied on weekly, biweekly and monthly aggregated series to yield an ensemble of daily tracer realizations. Daily tracer concentrations downscaled from a biweekly series had average (+/- standard deviation) absolute errors of 1.69‰ (1.61‰) for δ 2 H and 0.23‰ (0.24‰) for δ 18 O relative to observations. The results suggest coarsely sampled precipitation tracers can be accurately downscaled to daily values. This method may be extended to other geochemical tracers in order to generate downscaled datasets needed to drive complex, fine-scale models of hydrometeorological processes. 

Stable isotope ratios of hydrogen and oxygen have been applied to water cycle research for over 60 years. Over the past two decades, however, new data, data compilations, and quantitative methods have supported the application of isotopic data to address large-scale water cycle problems. Recent results have demonstrated the impact of climate variation on atmospheric water cycling, provided constraints on continental- to global-scale land-atmosphere water vapor fluxes, revealed biases in the sources of runoff in hydrological models, and illustrated regional patterns of water use and management by people. In the past decade, global isotopic observations have spurred new debate over the role of soils in the water cycle, with potential to impact both ecological and hydrological theory. Many components of the water cycle remain underrepresented in isotopic databases. Increasing accessibility of analyses and improved platforms for data sharing will refine and grow the breadth of these contributions in the future. ▪ Isotope ratios in water integrate information on hydrological processes over scales from cities to the globe. ▪ Tracing water with isotopes helps reveal the processes that govern variability in the water cycle and may govern future global changes. ▪ Improvements in instrumentation, data sharing, and quantitative analysis have advanced isotopic water cycle science over the past 20 years. 

The hydrologic cycle couples the Earth's energy and carbon budgets through evaporation, moisture transport, and precipitation. Despite a wealth of observations and models, fundamental limitations remain in our capacity to deduce even the most basic properties of the hydrological cycle, including the spatial pattern of the residence time (RT) of water in the atmosphere and the mean distance traveled from evaporation sources to precipitation sinks. Meanwhile, geochemical tracers such as stable water isotope ratios provide a tool to probe hydrological processes, yet their interpretation remains equivocal despite several decades of use. As a result, there is a need for new mechanistic tools that link variations in water isotope ratios to underlying hydrological processes. Here we present a new suite of “process‐oriented tags,” which we use to explicitly trace hydrological processes within the isotopically enabled Community Atmosphere Model, version 6 (iCAM6). Using these tags, we test the hypotheses that precipitation isotope ratios respond to parcel rainout, variations in atmospheric RT, and preserve information regarding meteorological conditions during evaporation. We present results for a historical simulation from 1980 to 2004, forced with winds from the ERA5 reanalysis. We find strong evidence that precipitation isotope ratios record information about atmospheric rainout and meteorological conditions during evaporation, but little evidence that precipitation isotope ratios vary with water vapor RT. These new tracer methods will enable more robust linkages between observations of isotope ratios in the modern hydrologic cycle or proxies of past terrestrial environments and the environmental processes underlying these observations.

 

Mechanistic representations of biogeochemical processes in ecosystem models are rapidly advancing, requiring advancements in model evaluation approaches. Here we quantify multiple aspects of model functional performance to evaluate improved process representations in ecosystem models. We compare semi‐empirical stomatal models with hydraulic constraints against more mechanistic representations of stomatal and hydraulic functioning at a semi‐arid pine site using a suite of metrics and analytical tools. We find that models generally perform similarly under unstressed conditions, but performance diverges under atmospheric and soil drought. The more empirical models better capture synergistic information flows between soil water potential and vapor pressure deficit to transpiration, while the more mechanistic models are overly deterministic. Although models can be parameterized to yield similar functional performance, alternate parameterizations could not overcome structural model constraints that underestimate the unique information contained in soil water potential about transpiration. Additionally, both multilayer canopy and big‐leaf models were unable to capture the magnitude of canopy temperature divergence from air temperature, and we demonstrate that errors in leaf temperature can propagate to considerable error in simulated transpiration. This study demonstrates the value of merging underutilized observational data streams with emerging analytical tools to characterize ecosystem function and discriminate among model process representations.

 

The isotopic composition of precipitation is used to trace water cycling and climate change, but interpretations of the environmental information recorded in central Andean precipitation isotope ratios are hindered by a lack of multi‐year records, poor spatial distribution of observations, and a predominant focus on Rayleigh distillation. To better understand isotopic variability in central Andean precipitation, we present a three‐year record of semimonthly δ¹⁸O_pand δ²H_pvalues from 15 stations in southern Peru and triple oxygen isotope data, expressed as ∆′¹⁷O_p, from 32 precipitation samples. Consistent with previous work, we find that elevation correlates negatively with δ¹⁸O_pand that seasonal δ¹⁸O_pvariations are related to upstream rainout and local convection. Spatial δ¹⁸O_pvariations and atmospheric back trajectories show that both eastern‐ and western‐derived air masses bring precipitation to southern Peru. Seasonal d‐excess_pcycles record moisture recycling and relative humidity at remote moisture sources, and both d‐excess_pand ∆′¹⁷O_pclearly differentiate evaporated and non‐evaporated samples. These results begin to establish the natural range of unevaporated ∆′¹⁷O_pvalues in the central Andes and set the foundation for future paleoclimate and paleoaltimetry studies in the region. This study highlights the hydrologic understanding that comes from a combination of δ¹⁸O_p, d‐excess_p, and ∆′¹⁷O_pdata and helps identify the evaporation, recycling, and rainout processes that drive water cycling in the central Andes.