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  1. Abstract

    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.

     
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  2. Abstract

    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 δ18Opand δ2Hpvalues from 15 stations in southern Peru and triple oxygen isotope data, expressed as ∆′17Op, from 32 precipitation samples. Consistent with previous work, we find that elevation correlates negatively with δ18Opand that seasonal δ18Opvariations are related to upstream rainout and local convection. Spatial δ18Opvariations and atmospheric back trajectories show that both eastern‐ and western‐derived air masses bring precipitation to southern Peru. Seasonal d‐excesspcycles record moisture recycling and relative humidity at remote moisture sources, and both d‐excesspand ∆′17Opclearly differentiate evaporated and non‐evaporated samples. These results begin to establish the natural range of unevaporated ∆′17Opvalues 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 δ18Op, d‐excessp, and ∆′17Opdata and helps identify the evaporation, recycling, and rainout processes that drive water cycling in the central Andes.

     
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  3. Stable isotope ratios of carbon and oxygen, and mass percentage data of various components of ponderosa pine individuals in Big Cottonwood Canyon, Utah to accompany a manuscript published in Oecologia.

    Two or three branches from five ponderosa pine individuals in Big Cottonwood Canyon, Utah were sampled in February, June, July, and September of 2019. Samples were processed to get mass percentages of sugars, starch, and cellulose in the branch and in needle segments. Needle values are presented in segments, with values for the bottom, middle, and top thirds of the needle. Carbon and oxygen stable isotope ratios were determined from ground bulk samples, as well as the sugar and cellulose fractions. Carbon isotope ratios are presented with respect to VPDB standard while oxygen isotope ratios are presented with respect to the VSMOW standard.
     
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  4. null (Ed.)
    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. 
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  5. This dataset contains monthly average output files from the iCAM6 simulations used in the manuscript "Enhancing understanding of the hydrological cycle via pairing of process-oriented and isotope ratio tracers," in review at the Journal of Advances in Modeling Earth Systems. A file corresponding to each of the tagged and isotopic variables used in this manuscript is included. Files are at 0.9° latitude x 1.25° longitude, and are in NetCDF format. Data from two simulations are included: 1) a simulation where the atmospheric model was "nudged" to ERA5 wind and surface pressure fields, by adding an additional tendency (see section 3.1 of associated manuscript), and 2) a simulation where the atmospheric state was allowed to freely evolve, using only boundary conditions imposed at the surface and top of atmosphere. Specific information about each of the variables provided is located in the "usage notes" section below. Associated article abstract: 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.   Details about the simulation setup can be found in section 3 of the associated open-source manuscript, "Enhancing understanding of the hydrological cycle via pairing of process‐oriented and isotope ratio tracers." In brief, we conducted two simulations of the atmosphere from 1980-2004 using the isotope-enabled version of the Community Atmosphere Model 6 (iCAM6) at 0.9x1.25° horizontal resolution, and with 30 vertical hybrid layers spanning from the surface to ~3 hPa. In the first simulation, wind and surface pressure fields were "nudged" toward the ERA5 reanalysis dataset by adding a nudging tendency, preventing the model from diverging from observed/reanalysis wind fields. In the second simulation, no additional nudging tendency was included, and the model was allowed to evolve 'freely' with only boundary conditions provided at the top (e.g., incoming solar radiation) and bottom (e.g., observed sea surface temperatures) of the model. In addition to the isotopic variables, our simulation included a suite of 'process-oriented tracers,' which we describe in section 2 of the manuscript. These variables are meant to track a property of water associated with evaporation, condensation, or atmospheric transport. Metadata are provided about each of the files below; moreover, since the attached files are NetCDF data - this information is also provided with the data files. NetCDF metadata can be accessed using standard tools (e.g., ncdump). Each file has 4 variables: the tagged quantity, and the associated coordinate variables (time, latitude, longitude). The latter three are identical across all files, only the tagged quantity changes. Twelve files are provided for the nudged simulation, and an additional three are provided for the free simulations: Nudged simulation files iCAM6_nudged_1980-2004_mon_RHevap: Mass-weighted mean evaporation source property: RH (%) with respect to surface temperature. iCAM6_nudged_1980-2004_mon_Tevap: Mass-weighted mean evaporation source property: surface temperature in Kelvin iCAM6_nudged_1980-2004_mon_Tcond: Mass-weighted mean condensation property: temperature (K) iCAM6_nudged_1980-2004_mon_columnQ: Total (vertically integrated) precipitable water (kg/m2).  Not a tagged quantity, but necessary to calculate depletion times in section 4.3 (e.g., Fig. 11 and 12). iCAM6_nudged_1980-2004_mon_d18O: Precipitation d18O (‰ VSMOW) iCAM6_nudged_1980-2004_mon_d18Oevap_0: Mass-weighted mean evaporation source property - d18O of the evaporative flux (e.g., the 'initial' isotope ratio prior to condensation), (‰ VSMOW) iCAM6_nudged_1980-2004_mon_dxs: Precipitation deuterium excess (‰ VSMOW) - note that precipitation d2H can be calculated from this file and the precipitation d18O as d2H = d-excess - 8*d18O. iCAM6_nudged_1980-2004_mon_dexevap_0: Mass-weighted mean evaporation source property - deuterium excess of the evaporative flux iCAM6_nudged_1980-2004_mon_lnf: Integrated property - ln(f) calculated from the constant-fractionation d18O tracer (see section 3.2). iCAM6_nudged_1980-2004_mon_precip: Total precipitation rate in m/s. Note there is an error in the metadata in this file - it is total precipitation, not just convective precipitation. iCAM6_nudged_1980-2004_mon_residencetime: Mean atmospheric water residence time (in days). iCAM6_nudged_1980-2004_mon_transportdistance: Mean atmospheric water transport distance (in km). Free simulation files iCAM6_free_1980-2004_mon_d18O: Precipitation d18O (‰ VSMOW) iCAM6_free_1980-2004_mon_dxs: Precipitation deuterium excess (‰ VSMOW) - note that precipitation d2H can be calculated from this file and the precipitation d18O as d2H = d-excess - 8*d18O. iCAM6_free_1980-2004_mon_precip: Total precipitation rate in m/s. Note there is an error in the metadata in this file - it is total precipitation, not just convective precipitation. 
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