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In alluvial aquifers with near-neutral pH and high dissolved arsenic (As) concentrations, the presence and character of sedimentary organic matter (SOM) regulates As mobility by serving as an energetically variable source of electrons for redox reactions or forming As–Fe-OM complexes. Near tidally and seasonally fluctuating rivers, the hyporheic zone (HZ), which embodies the mixing zone between oxic river water and anoxic shallow groundwater, may precipitate (or dissolve) iron (Fe)-oxides which sequester (or mobilize) As. To understand what is driving the mobilization of As within a shallow aquifer and riverbank sands adjacent to the tidally fluctuating Meghna River, we characterized the chemical reactivity of SOM from the sands, and a silt and clay layer, underlying the HZ and aquifer, respectively. Dissolved As (50–500 μg/L) and Fe (1–40 mg/L) concentrations increase with depth within the shallow aquifer. Similar vertical As and Fe concentration gradients were observed within the riverbank sands where concentrations of the products of reductive dissolution of Fe-oxides increase with proximity to the silt layer. Compared to all other sediments, the SOM in the clay aquitard contains older, more recalcitrant, terrestrially-derived material with high proportions of aromatic carboxylate functional groups. The shallow silt layer contains fresher SOM with higher proportions of amides and more labile polysaccharide moieties. The SOM in both the riverbank and aquifer is terrestrially-derived and humic-like. The labile SOM from the silt layer drives the microbially mediated reductive dissolution of As-bearing Fe-oxides in the HZ. In contrast, the carboxylate-rich SOM from the clay aquitard maintains dissolved As concentrations at the base of the aquifer by complexing with soluble As and Fe. This highlights that SOM-rich fine (silt or clay) layers in the Bengal basin drive As and Fe mobility, however, the specific processes mobilizing As and Fe depend on the lability of the SOM. 

Abstract Fresh submarine groundwater discharge (FSGD) can deliver significant fluxes of water and solutes from land to sea. In the Arctic, which accounts for ∼34% of coastlines globally, direct observations and knowledge of FSGD are scarce. Through integration of observations and process‐based models, we found that regardless of ice‐bonded permafrost depth at the shore, summer SGD flow dynamics along portions of the Beaufort Sea coast of Alaska are similar to those in lower latitudes. Calculated summer FSGD fluxes in the Arctic are generally higher relative to low latitudes. The FSGD organic carbon and nitrogen fluxes are likely larger than summer riverine input. The FSGD also has very high CO₂making it a potentially significant source of inorganic carbon. Thus, the biogeochemistry of Arctic coastal waters is potentially influenced by groundwater inputs during summer. These water and solute fluxes will likely increase as coastal permafrost across the Arctic thaws. 

Abstract Submarine groundwater discharge (SGD) in volcanic areas commonly exhibits high temperatures, concentrations of metals and CO₂, and acidity, all of which could affect sensitive coastal ecosystems. Identifying and quantifying volcanic SGD is crucial yet challenging because the SGD might be both discrete, through fractured volcanic rock, and diffuse. At a volcanic area in the Philippines, the novel combination of satellite and drone‐based thermal infrared remote sensing, ground‐based fiber‐optic distributed temperature sensing, and in situ thermal profiling in coastal sediment identified the multi‐scale nature of SGD and quantified fluxes. We identified SGD across ∼30 km of coastline. The different approaches revealed numerous SGD signals from the intertidal zone to about a hundred meters offshore. In active seepage areas, temperatures peaked at 80°C, and Darcy fluxes were as high as 150 cm/d. SGD is therefore locally prominent and regionally important across the study area. 

Abstract Terrestrial groundwater travels through subterranean estuaries before reaching the sea. Groundwater‐derived nutrients drive coastal water quality, primary production, and eutrophication. We determined how dissolved inorganic nitrogen (DIN), dissolved inorganic phosphorus (DIP), and dissolved organic nitrogen (DON) are transformed within subterranean estuaries and estimated submarine groundwater discharge (SGD) nutrient loads compiling > 10,000 groundwater samples from 216 sites worldwide. Nutrients exhibited complex, nonconservative behavior in subterranean estuaries. Fresh groundwater DIN and DIP are usually produced, and DON is consumed during transport. Median total SGD (saline and fresh) fluxes globally were 5.4, 2.6, and 0.18 Tmol yr⁻¹for DIN, DON, and DIP, respectively. Despite large natural variability, total SGD fluxes likely exceed global riverine nutrient export. Fresh SGD is a small source of new nutrients, but saline SGD is an important source of mostly recycled nutrients. Nutrients exported via SGD via subterranean estuaries are critical to coastal biogeochemistry and a significant nutrient source to the oceans.