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Abstract The tidal tributaries of the lower Chesapeake Bay experience seasonally recurring harmful algal blooms and the significance of submarine groundwater discharge (SGD) as a nutrient vector is largely unknown. Here, we determined seasonal SGD nutrient loads in two tributaries with contrasting hydrodynamic conditions, river‐fed (York River) vs. tidally dominated (Lafayette River). Radon surveys were performed in each river to quantify SGD at the embayment‐scale during spring and fall 2021. Total SGD was determined from a²²²Rn mass balance and Monte Carlo simulations. Submarine groundwater discharge rates differed by a factor of two during spring (Lafayette = 11 ± 17 cm d⁻¹; York = 6 ± 10 cm d⁻¹) and a factor of six during fall (Lafayette = 19 ± 27 cm d⁻¹; York = 3 ± 7 cm d⁻¹). Groundwater N concentrations and fluxes varied seasonally in the York (4–7 mmol N m⁻²d⁻¹). In the Lafayette River, seasonal N fluxes (22–37 mmol N m⁻²d⁻¹) were driven by seasonal water exchange rates, likely due to recurrent saltwater intrusion. Submarine groundwater discharge–derived nutrient fluxes were orders of magnitude greater than riverine inputs and runoff in each system. Additionally, sediment N removal by denitrification and anaerobic ammonium oxidation would only remove ~ 1–11% of dissolved inorganic nitrogen supplied through SGD. The continued recurrence of harmful algal blooms in the Bay's tidal tributaries may be indicative of an under‐accounting of submarine groundwater‐borne nutrient sources. This study highlights the importance of including SGD in water quality models used to advise restoration efforts in the Chesapeake Bay region and beyond. 

Loss of tidal wetlands is a world-wide phenomenon. Many factors may contribute to such loss, but among them are geochemical stressors such as exposure of the marsh plants to elevated levels on hydrogen sulfide in the pore water of the marsh peat. Here we report the results of a study of the geochemistry of iron and sulfide at different seasons in unrestored (JoCo) and partially restored (Big Egg) salt marshes in Jamaica Bay, a highly urbanized estuary in New York City where the loss of salt marsh area has accelerated in recent years. The spatial and temporal 2-dimensional distribution patterns of dissolved Fe 2+ and H 2 S in salt marshes were in situ mapped with high resolution planar sensors for the first time. The vertical profiles of Fe 2+ and hydrogen sulfide, as well as related solutes and redox potentials in marsh were also evaluated by sampling the pore water at discrete depths. Sediment cores were collected at various seasons and the solid phase Fe, S, N, C, and chromium reducible sulfide in marsh peat at discrete depths were further investigated in order to study Fe and S cycles, and their relationship to the organic matter cycling at different seasons. Our results revealed that the redox sensitive elements Fe 2+ and S 2– showed significantly heterogeneous and complex three dimensional distribution patterns in salt marsh, over mm to cm scales, directly associated with the plant roots due to the oxygen leakage from roots and redox diagenetic reactions. We hypothesize that the oxic layers with low/undetected H 2 S and Fe 2+ formed around roots help marsh plants to survive in the high levels of H 2 S by reducing sulfide absorption. The overall concentrations of Fe 2+ and H 2 S and distribution patterns also seasonally varied with temperature change. H 2 S level in JoCo sampling site could change from <0.02 mM in spring to >5 mM in fall season, reflecting significantly seasonal variation in the rates of bacterial oxidation of organic matter at this marsh site. Solid phase Fe and S showed that very high fractions of the diagenetically reactive iron at JoCo and Big Egg were associated with pyrite that can persist for long periods in anoxic sediments. This implies that there is insufficient diagenetically reactive iron to buffer the pore water hydrogen sulfide through formation of iron sulfides at JoCo and Big Egg.