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Abstract Historically, clumped isotope thermometry (T(∆₄₇)) of soil carbonates has been interpreted to represent a warm‐season soil temperature based dominantly on coarse‐grained soils. Additionally, T(∆₄₇) allows the calculation of the oxygen isotope composition of soil water (δ¹⁸O_w) in the past using the temperature‐dependent fractionation factor between soil water and pedogenic carbonate, but previous work has not measured δ¹⁸O_wvalues with which to compare to these archives. Here, we present clumped isotope thermometry of modern soil carbonates from three soils in Colorado and Nebraska, USA, that have a fine‐to‐medium grain size, contain clay, and are representative of many carbonate‐bearing paleosols preserved in the rock record. At two of the three sites, Briggsdale, CO and Seibert, CO, T(∆₄₇) overlaps with mean annual soil temperature (MAST), and the calculated δ¹⁸O_woverlaps within uncertainty with measured δ¹⁸O_wat carbonate bearing depths. At the third site, in Oglala National Grassland, NE, mean T(∆₄₇) is 8–11°C warmer than MAST, and the calculated δ¹⁸O_whas a significantly higher isotope value than any observations of δ¹⁸O_w. At all three sites, even in the fall season, δ¹⁸O_wvalues at carbonate bearing depths overlap with spring rainfall δ¹⁸O_w, and there is little to no evaporative enrichment of δ²H_wand δ¹⁸O_wvalues. These data challenge long‐held assumptions that all pedogenic carbonate records a warm‐season bias, and that δ¹⁸O_wat carbonate‐bearing depths is affected by evaporative enrichment. 

Abstract. Soil water isotope datasets are useful for understanding connections between the hydrosphere, atmosphere, biosphere, and geosphere. However, they have been underproduced because of the technical challenges associated with collecting those datasets. Here, we present the results of testing and automation of the Soil Water Isotope Storage System (SWISS). The unique innovation of the SWISS is that we are able to automatically collect water vapor from the critical zone at a regular time interval and then store that water vapor until it can be measured back in a laboratory setting. Through a series of quality assurance and quality control tests, we tested whether the SWISS is resistant to both atmospheric intrusion and leaking in both laboratory and field settings. We assessed the accuracy and precision of the SWISS through a series of experiments in which water vapor of known composition was introduced into the flasks, stored for 14 d, and then measured. From these experiments, after applying an offset correction to report our values relative to Vienna Standard Mean Ocean Water (VSMOW), we assess the precision of the SWISS to be ±0.9 ‰ and ±3.7 ‰ for δ18O and δ2H, respectively. We deployed three SWISS units at three different field sites to demonstrate that the SWISS stores water vapor reliably enough that we are able to differentiate dynamics both between the sites as well within a single soil column. Overall, we demonstrate that the SWISS retains the stable isotope composition of soil water vapor for long enough to allow researchers to address a wide range of ecohydrologic questions.