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Radium‐226(²²⁶Ra) and barium (Ba) exhibit similar chemical behaviors and distributions in the marine environment, serving as valuable tracers of water masses, ocean mixing, and productivity. Despite their similar distributions, these elements originate from distinct sources and undergo disparate biogeochemical cycles, which might complicate the use of these tracers. In this study, we investigate these processes by analyzing a full‐depth ocean section of²²⁶Ra activities (T_1/2 = 1,600 years) and barium concentrations obtained from samples collected along the US GEOTRACES GP15 Pacific Meridional Transect during September–November 2018, spanning from Alaska to Tahiti. We find that surface waters possess low levels of²²⁶Ra and Ba due to export of sinking particulates, surpassing inputs from the continental margins. In contrast, deep waters have higher²²⁶Ra activities and Ba concentrations due to inputs from particle regeneration and sedimentary sources, with²²⁶Ra inputs primarily resulting from the decay of²³⁰Th in sediments. Further, dissolved²²⁶Ra and Ba exhibit a strong correlation along the GP15 section. To elucidate the drivers of the correlation, we used a water mass analysis, enabling us to quantify the influence of water mass mixing relative to non‐conservative processes. While a significant fraction of each element's distribution can be explained by conservative mixing, a considerable fraction cannot. The balance is driven using non‐conservative processes, such as sedimentary, rivers, or hydrothermal inputs, uptake and export by particles, and particle remineralization. Our study demonstrates the utility of²²⁶Ra and Ba as valuable biogeochemical tracers for understanding ocean processes, while shedding light on conservative and myriad non‐conservative processes that shape their respective distributions.

Marine tracer studies indicate that large volumes of saline groundwater discharge to the ocean in passive margin settings. These results have not found widespread recognition because the location and cause(s) of this submarine groundwater discharge (SGD) are unclear. Here we report observations from a new long‐term seafloor monitoring network in the South Atlantic Bight that support large‐scale SGD far from shore. In the study area near Charleston, South Carolina, we determined hydrostratigraphy via vibracoring and chirp seismic surveys, collected water samples from seafloor wells, and used heat as a tracer to monitor SGD. We detected significant pulses of saline SGD issuing from the seafloor 10–15 km from shore. These pulses coincided with abrupt sea level declines of up to 30 cm. Based on an analysis of marine conditions at the time, we propose that upwelling‐favorable winds depressed sea level in the region, causing saline groundwater to discharge from confined coastal aquifers that connect land and ocean. The combination of stacked confined aquifers and variations in sea level are nearly ubiquitous in passive coastal margins. This previously overlooked combination can explain a wide range of other published observations and promotes more dynamic flows than simple tidal fluctuations. This new mechanism may explain Ra tracer signals in the coastal Atlantic Ocean and supports significant nutrient inputs to the ocean. These large natural geochemical fluxes may be sensitive to groundwater usage on land.

Submarine groundwater discharge (SGD) plays a critical role in coastal and ocean biogeochemistry. Elucidating spatially and temporally heterogeneous SGD fluxes is difficult. Here we use radium isotopes to explore the external sources and mixing regime along the eastern coast of South Africa. We demonstrate that the long‐lived radium isotope compositions are controlled by low inputs of low‐ and high‐salinity terrestrial groundwater. While activities of²²⁸Ra and²²⁶Ra in beach porewaters are similar to coastal waters,²²⁴Ra is enriched by inputs of²²⁸Th from coastal seawater. Porewater ages, based on the production of²²⁴Ra from²²⁸Th, range from 0.3 to 2.3 days, indicating rapid flushing of the beach system. Unlike radium, however, nutrients follow a more complex pathway. We hypothesize that high total dissolved nitrogen (TDN) and phosphorus concentrations in beach porewaters (TDN ranges from 1 to >700 μM) and the coastal ocean (TDN ranges from 1 to >40 μM) are derived from a source not enriched in radium. We speculate that this source is terrestrial water flowing below the dune barrier at depths exceeding our beach sampling depths. This water likely flows upward through breaches in the confining layer into the beach or enters the ocean directly through paleochannels. The presence of high nutrient concentrations in the coastal ocean unaccompanied by high²²⁸Ra activities leads to the hypothesis of this additional nutrient source. These combined inputs may be of considerable importance to the coastal ecology of southeastern Africa, an oligotrophic ecosystem dominated by the nutrient‐poor Agulhas Current.

Radium isotopes are produced through the decay of thorium in sediments and are soluble in seawater; thus, they are useful for tracing ocean boundary‐derived inputs to the ocean. Here we apply radium isotopes to study continental inputs and water residence times in the Arctic Ocean, where land‐ocean interactions are currently changing in response to rising air and sea temperatures. We present the distributions of radium isotopes measured on the 2015 U.S. GEOTRACES transect in the Western Arctic Ocean and combine this data set with historical radium observations in the Chukchi Sea and Canada Basin. The highest activities of radium‐228 were observed in the Transpolar Drift and the Chukchi shelfbreak jet, signaling that these currents are heavily influenced by interactions with shelf sediments. The ventilation of the halocline with respect to inputs from the Chukchi shelf occurs on time scales of ≤19–23 years. Intermediate water ventilation time scales for the Makarov and Canada Basins were determined to be ~20 and >30 years, respectively, while deep water residence times in these basins were on the order of centuries. The radium distributions and residence times described in this study serve as a baseline for future studies investigating the impacts of climate change on the Arctic Ocean.

A major surface circulation feature of the Arctic Ocean is the Transpolar Drift (TPD), a current that transports river‐influenced shelf water from the Laptev and East Siberian Seas toward the center of the basin and Fram Strait. In 2015, the international GEOTRACES program included a high‐resolution pan‐Arctic survey of carbon, nutrients, and a suite of trace elements and isotopes (TEIs). The cruises bisected the TPD at two locations in the central basin, which were defined by maxima in meteoric water and dissolved organic carbon concentrations that spanned 600 km horizontally and ~25–50 m vertically. Dissolved TEIs such as Fe, Co, Ni, Cu, Hg, Nd, and Th, which are generally particle‐reactive but can be complexed by organic matter, were observed at concentrations much higher than expected for the open ocean setting. Other trace element concentrations such as Al, V, Ga, and Pb were lower than expected due to scavenging over the productive East Siberian and Laptev shelf seas. Using a combination of radionuclide tracers and ice drift modeling, the transport rate for the core of the TPD was estimated at 0.9 ± 0.4 Sv (10⁶ m³ s⁻¹). This rate was used to derive the mass flux for TEIs that were enriched in the TPD, revealing the importance of lateral transport in supplying materials beneath the ice to the central Arctic Ocean and potentially to the North Atlantic Ocean via Fram Strait. Continued intensification of the Arctic hydrologic cycle and permafrost degradation will likely lead to an increase in the flux of TEIs into the Arctic Ocean.