Simulated Biogeochemical Effects of Seawater Restoration on Diked Salt Marshes, Cape Cod National Seashore, Massachusetts, U.S

• Published in: Soil systems Vol. 9; no. 3; p. 89
• Main Author: Brown, Craig J.
• Format: Journal Article
• Language: English
• Published: 08.08.2025
• ISSN: 2571-8789; 2571-8789
• DOI: 10.3390/soilsystems9030089

Efforts have been underway worldwide to reintroduce seawater to many historically diked salt marshes for restoration of tidal flow and associated estuarine habitat. Seawater restoration to a diked Cape Cod marsh was simulated using the computer program PHREEQC based on previously conducted microcosm experiments to better understand the associated timing and sequence of multiple biogeochemical reactions and their implications to aquatic health. Model simulations show that acidic, reducing waters with high concentrations of sorbed ferrous iron (Fe[II]), aluminum (Al), sulfide (S2−), ammonia (NH4+ + NH3), and phosphate (PO43−) are released through desorption and sediment weathering following salination that can disrupt aquatic habitat. Models were developed for one-dimensional reactive transport of solutes in diked, flooded (DF) marsh sediments and subaerially exposed, diked, drained (DD) sediments by curve matching porewater solute concentrations and adjusting the sedimentary organic matter (SOM) degradation rates based on the timing and magnitude of Fe(II) and S2− concentrations. Simulated salination of the DD sediments, in particular, showed a large release of Al, Fe(II), NH4+, and PO43−; the redox shift to reductive dissolution provided higher rates of SOM oxidation. The sediment type, iron source, and seasonal timing associated with seawater restoration can affect the chemical speciation and toxicity of constituents to aquatic habitat. The constituents of concern and their associated complex biogeochemical reactions simulated in this study are directly relevant to the increasingly common coastal marsh salination, either through tidal restoration or rising sea level.