Search for: All records

Billions of people rely upon groundwater for drinking water and agriculture, yet predicting how climate change may affect aquifer storage remains challenging. To gain insight beyond the short historical record, we reconstruct changes in groundwater levels in western North America during the last glacial termination (LGT, ~20 to 11 thousand years ago) using noble gas isotopes. Our reconstructions indicate remarkable stability of water table depth in a Pacific Northwest aquifer throughout the LGT despite increasing precipitation, closely matching independent Earth system model (ESM) simulations. In the American Southwest, ESM simulations and noble gas isotopes both suggest a pronounced LGT decline in water table depth in in response to decreasing precipitation, indicating distinct regional groundwater responses to climate. Despite the hydrologic simplicity of ESMs, their agreement with proxy reconstructions of past water table depth suggests that these models hold value in understanding groundwater dynamics and projecting large-scale aquifer responses to climate forcing. 

These data correspond to the article “Deep Nitrogen Fluxes and Sources Constrained by Arc Lava Phenocrysts” by Hudak et al. submitted to Geophysical Research Letters. Table S1 includes N-He-Ar data for FIs in phenocrysts from mafic are lavas and tephras. Table S2 contains the corrected N2/3He data used for volcanic arc N flux calculations and the arc-averaged mean N arc flux. Table S3 summarizes previous literature estimates of N fluxes and the data used for those calculations. Table S4 provides the N concentrations, He concentrations, N isotope compositions of the mantle, sediments, and altered oceanic crust, as well as sediment thicknesses. Finally, Table S5 gives information about the sources of the mineral separates used for these analyses. 

Ubiquitous fractionation processes in the subsurface obscure mantle-derived volatile signals in hydrothermal systems. 

Abstract Halogens are primarily located within surface reservoirs of the Earth; as such they have proven to be effective tracers for the identification of subducted volatiles within the mantle. Subducting lithologies exhibit a wide variety of halogen compositions, yet the mantle maintains a fairly uniform signature, suggesting halogens may be homogenized during subduction to the mantle or during eruption. Here we present halogen (Cl, Br, and I), K, noble gas, and major and trace element data on olivines from three seamounts along the Hawaiian‐Emperor seamount chain to determine if the deep mantle source has retained evidence of halogen heterogeneities introduced through subduction. High Ni contents indicate that the Hawaiian‐Emperor mantle source contains a recycled oceanic crust component in the form of pyroxenite, which increases from the 46% in the oldest (Detroit) to 70% in the younger seamount (Koko). Detroit seamount retains mid‐ocean ridge basalts (MORB)‐like Br/Cl and I/Cl, while the Br/Cl and I/Cl of Suiko and Koko seamounts are higher than MORB and similar to altered oceanic crust and dehydrated serpentinite. Helium isotopes show a similar evolution, from MORB‐like values at Detroit seamount toward higher values at Suiko and Koko seamounts. The correlation between pyroxenite contributions, Br/Cl, I/Cl, and³He/⁴He indicates that subducted material has been incorporated into the primordial undegassed Hawaiian mantle plume source. The identification of recycled oceanic crustal signatures in both the trace elements and halogens indicates that subduction and dehydration of altered oceanic crust may exert control on the cycling of volatile elements to the deep mantle.