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Abstract Marsh accretion models predict the resiliency of coastal wetlands and their ability to store carbon in the face of accelerating sea level rise. Most existing marsh accretion models are derived from two parent models: the Marsh Equilibrium Model, which formalizes the biophysical relationships between sea level rise, dominant macrophyte growth, and elevation change; and the Cohort Theory Model, which formalizes how carbon mass pools belowground contribute to soil volume expansion over time. While there are several existing marsh accretion models, the application of these models by a broader base of researchers and practitioners is hindered because of (a) limited descriptions of how empirically derived ecological mechanism informed the development of these models, (b) limitations in the ability to apply models to geographies with variable tidal regimes, and (c) a lack of open‐source code to apply models. Here, we provide for the first time an explicit description of a mathematical version of the Cohort Theory Model and a numerical version of a combined model: the Cohort Marsh Equilibrium Model (CMEM) with an accompanying open‐sourceRpackage,rCMEM. We show that, through this “depth‐aware” model, we can capture how tidal variation impacts broad patterns of marsh accretion and carbon sequestration across the United States. The application of this model will likely be imperative in predicting the fate and state of coastal wetlands and the ecosystem services they provide in an era of rapid environmental change. 

Abstract Heterotrophic activity, primarily driven by sulfate-reducing prokaryotes, has traditionally been linked to nitrogen fixation in the root zone of coastal marine plants, leaving the role of chemolithoautotrophy in this process unexplored. Here, we show that sulfur oxidation coupled to nitrogen fixation is a previously overlooked process providing nitrogen to coastal marine macrophytes. In this study, we recovered 239 metagenome-assembled genomes from a salt marsh dominated by the foundation plantSpartina alterniflora, including diazotrophic sulfate-reducing and sulfur-oxidizing bacteria. Abundant sulfur-oxidizing bacteria encode and highly express genes for carbon fixation (RuBisCO), nitrogen fixation (nifHDK) and sulfur oxidation (oxidative-dsrAB), especially in roots stressed by sulfidic and reduced sediment conditions. Stressed roots exhibited the highest rates of nitrogen fixation and expression level of sulfur oxidation and sulfate reduction genes. Close relatives of marine symbionts from theCandidatusThiodiazotropha genus contributed ~30% and ~20% of all sulfur-oxidizingdsrAand nitrogen-fixingnifKtranscripts in stressed roots, respectively. Based on these findings, we propose that the symbiosis betweenS. alternifloraand sulfur-oxidizing bacteria is key to ecosystem functioning of coastal salt marshes.