Abstract

Groundwater-derived solute fluxes to the ocean have long been assumed static and subordinate to riverine fluxes, if not neglected entirely, in marine isotope budgets. Here we present concentration and isotope data for Li, Mg, Ca, Sr, and Ba in coastal groundwaters to constrain the importance of groundwater discharge in mediating the magnitude and isotopic composition of terrestrially derived solute fluxes to the ocean. Data were extrapolated globally using three independent volumetric estimates of groundwater discharge to coastal waters, from which we estimate that groundwater-derived solute fluxes represent, at a minimum, 5% of riverine fluxes for Li, Mg, Ca, Sr, and Ba. The isotopic compositions of the groundwater-derived Mg, Ca, and Sr fluxes are distinct from global riverine averages, while Li and Ba fluxes are isotopically indistinguishable from rivers. These differences reflect a strong dependence on coastal lithology that should be considered a priority for parameterization in Earth-system models.

Highlights

  • Groundwater-derived solute fluxes to the ocean have long been assumed static and subordinate to riverine fluxes, if not neglected entirely, in marine isotope budgets

  • Recent models of global weatherability have emphasized the importance of silicate weathering in humid, low-latitude, tectonically-active regions10,11—the same regions modeled to account for the majority (55–68%) of global groundwater discharge[1,2,4]

  • The resultant fluxes represent, at a minimum, 5% of global riverine flux values, which suggests that terrestrially derived solute flux estimates of these elements should be upwardly revised

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Summary

Introduction

Groundwater-derived solute fluxes to the ocean have long been assumed static and subordinate to riverine fluxes, if not neglected entirely, in marine isotope budgets. Volumetric flux estimates of global meteoric groundwater discharge vary by an order of magnitude, equivalent to 0.7–6% of global river discharge[1,2,3,4,5] Despite this large uncertainty, several studies have attempted to constrain the magnitude and isotopic composition of groundwater-derived solute fluxes to the ocean using available data from local characterizations of groundwater chemistry[2,4,6,7,8,9]. The isotopic compositions of the global groundwater fluxes for these elements are not always identical to global riverine values

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