Abstract. Salinization, a widespread threat to the structure and ecological functioning of inland and coastal wetlands, is currently occurring at an unprecedented rate and geographic scale. The causes of salinization are diverse and include alterations to freshwater flows, land-clearance, irrigation, disposal of wastewater effluent, sea level rise, storm surges, and applications of de-icing salts. Climate change and anthropogenic modifications to the hydrologic cycle are expected to further increase the extent and severity of wetland salinization. Salinization alters the fundamental physicochemical nature of the soil-water environment, increasing ionic concentrations and altering chemical equilibria and mineral solubility. Increased concentrations of solutes, especially sulfate, alter the biogeochemical cycling of major elements including carbon, nitrogen, phosphorus, sulfur, iron, and silica. The effects of salinization on wetland biogeochemistry typically include decreased inorganic nitrogen removal (with implications for water quality and climate regulation), decreased carbon storage (with implications for climate regulation and wetland accretion), and increased generation of toxic sulfides (with implications for nutrient cycling and the health/functioning of wetland biota). Indeed, increased salt and sulfide concentrations induce physiological stress in wetland biota and ultimately can result in large shifts in wetland communities and their associated ecosystem functions. The productivity and composition of freshwater species assemblages will be highly altered, and there is a high potential for the disruption of existing interspecific interactions. Although there is a wealth of information on how salinization impacts individual ecosystem components, relatively few studies have addressed the complex and often non-linear feedbacks that determine ecosystem-scale responses or considered how wetland salinization will affect landscape-level processes. Although the salinization of wetlands may be unavoidable in many cases, these systems may also prove to be a fertile testing ground for broader ecological theories including (but not limited to): investigations into alternative stable states and tipping points, trophic cascades, disturbance-recovery processes, and the role of historical events and landscape context in driving community response to disturbance.

For decades, ecosystem scientists have used global warming potentials (GWPs) to compare the radiative forcing of various greenhouse gases to determine if ecosystems have a net warming or cooling effect on climate. On a conceptual basis, the continued use of GWPs by the ecological community may be untenable because the use of GWPs requires the implicit assumption that greenhouse gas emissions occur as a single pulse; this assumption is rarely justified in ecosystem studies. We present two alternate metrics-the sustained-flux global warming potential (SGWP, for gas emissions) and the sustained-flux global cooling potential (SGCP, for gas uptake)-for use when gas fluxes persist over time. The SGWP is generally larger than the GWP (by up to $40%) for both methane and nitrous oxide emissions, creating situations where the GWP and SGWP metrics could provide opposing interpretations about the climatic role of an ecosystem. Further, there is an asymmetry in methane and nitrous oxide dynamics between persistent emission and uptake situations, producing very different values for the SGWP vs. SGCP and leading to the conclusion that ecosystems that take up these gases are very effective at reducing radiative forcing. Although the new metrics are more realistic than the GWP for ecosystem fluxes, we further argue that even these metrics may be insufficient in the context of trying to understand the lifetime climatic role of an ecosystem. A dynamic modeling approach that has the flexibility to account for temporally variable rates of greenhouse gas exchange, and is not limited by a fixed time frame, may be more informative than the SGWP, SGCP, or GWP. Ultimately, we hope this article will stimulate discussion within the ecosystem science community about the most appropriate way(s) of assessing the role of ecosystems as regulators of global climate.

A mixing model derived from first principles describes the bulk density (BD) of intertidal wetland sediments as a function of loss on ignition (LOI). The model assumes that the bulk volume of sediment equates to the sum of self‐packing volumes of organic and mineral components or BD = 1/[LOI/k1 + (1‐LOI)/k2], where k1 and k2 are the self‐packing densities of the pure organic and inorganic components, respectively. The model explained 78% of the variability in total BD when fitted to 5075 measurements drawn from 33 wetlands distributed around the conterminous United States. The values of k1 and k2 were estimated to be 0.085 ± 0.0007 g cm−3 and 1.99 ± 0.028 g cm−3, respectively. Based on the fitted organic density (k1) and constrained by primary production, the model suggests that the maximum steady state accretion arising from the sequestration of refractory organic matter is ≤ 0.3 cm yr−1. Thus, tidal peatlands are unlikely to indefinitely survive a higher rate of sea‐level rise in the absence of a significant source of mineral sediment. Application of k2 to a mineral sediment load typical of East and eastern Gulf Coast estuaries gives a vertical accretion rate from inorganic sediment of 0.2 cm yr−1. Total steady state accretion is the sum of the parts and therefore should not be greater than 0.5 cm yr−1 under the assumptions of the model. Accretion rates could deviate from this value depending on variation in plant productivity, root:shoot ratio, suspended sediment concentration, sediment‐capture efficiency, and episodic events.

The impact of salt-water intrusion on microbial organic carbon (C) mineralization in tidal freshwater marsh (TFM) soils was investigated in a year-long laboratory experiment in which intact soils were exposed to a simulated tidal cycle of freshwater or dilute salt-water. Gas fluxes [carbon dioxide (CO 2 ) and methane (CH 4 )], rates of microbial processes (sulfate reduction and methanogenesis), and porewater and solid phase biogeochemistry were measured throughout the experiment. Flux rates of CO 2 and, surprisingly, CH 4 increased significantly following salt-water intrusion, and remained elevated relative to freshwater cores for 6 and 5 months, respectively. Following saltwater intrusion, rates of sulfate reduction increased significantly and remained higher than rates in the freshwater controls throughout the experiment. Rates of acetoclastic methanogenesis were higher than rates of hydrogenotrophic methanogenesis, but the rates did not differ by salinity treatment. Soil organic C content decreased significantly in soils experiencing salt-water intrusion. Estimates of total organic C mineralized in freshwater and salt-water amended soils over the 1-year experiment using gas flux measurements (18.2 and 24.9 mol C m -2 , respectively) were similar to estimates obtained from microbial rates (37.8 and 56.2 mol C m -2 , respectively), and to losses in soil organic C content (0 and 44.1 mol C m -2 , respectively). These findings indicate that salt-water intrusion stimulates microbial decomposition, accelerates the loss of organic C from TFM soils, and may put TFMs at risk of permanent inundation.

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