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Abstract Variations in estuarine carbonate chemistry can have critical impacts on marine calcifying organisms, yet the drivers of this variability are difficult to quantify from observations alone, due to the strong spatiotemporal variability of these systems. Terrestrial runoff and wetland processes vary year to year based on local precipitation, and estuarine processes are often strongly modulated by tides. In this study, a 3D-coupled hydrodynamic-biogeochemical model is used to quantify the controls on the carbonate system of a coastal plain estuary, specifically the York River estuary. Experiments were conducted both with and without tidal wetlands. Results show that on average, wetlands account for 20–30% of total alkalinity (TA) and dissolved inorganic carbon (DIC) fluxes into the estuary, and double-estuarine CO₂outgassing. Strong quasi-monthly variability is driven by the tides and causes fluctuations between net heterotrophy and net autotrophy. On longer time scales, model results show that in wetter years, lower light availability decreases primary production relative to biological respiration (i.e., greater net heterotrophy) resulting in substantial increases in CO₂outgassing. Additionally, in wetter years, advective exports of DIC and TA to the Chesapeake Bay increase by a factor of three to four, resulting in lower concentrations of DIC and TA within the estuary. Quantifying the impacts of these complex drivers is not only essential for a better understanding of coastal carbon and alkalinity cycling, but also leads to an improved assessment of the health and functioning of coastal ecosystems both in the present day and under future climate change. 

Abstract Global carbon dioxide (CO₂) evasion from inland waters (rivers, lakes, and reservoirs) and carbon (C) export from land to oceans constitute critical terms in the global C budget. However, the magnitudes, spatiotemporal patterns, and underlying mechanisms of these fluxes are poorly constrained. Here, we used a coupled terrestrial–aquatic model to assess how multiple changes in climate, land use, atmospheric CO₂concentration, nitrogen (N) deposition, N fertilizer and manure applications have affected global CO₂evasion and riverine C export along the terrestrial‐aquatic continuum. We estimate that terrestrial C loadings, riverine C export, and CO₂evasion in the preindustrial period (1800s) were 1,820 ± 507 (mean ± standard deviation), 765 ± 132, and 841 ± 190 Tg C yr⁻¹, respectively. During 1800–2019, multifactorial global changes caused an increase of 25% (461 Tg C yr⁻¹) in terrestrial C loadings, reaching 2,281 Tg C yr⁻¹in the 2010s, with 23% (104 Tg C yr⁻¹) of this increase exported to the ocean and 59% (273 Tg C yr⁻¹) being emitted to the atmosphere. Our results showed that global inland water recycles and exports nearly half of the net land C sink into the atmosphere and oceans, highlighting the important role of inland waters in the global C balance, an amount that should be taken into account in future C budgets. Our analysis supports the view that a major feature of the global C cycle–the transfer from land to ocean–has undergone a dramatic change over the last two centuries as a result of human activities.