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Abstract Salt marshes can attenuate nutrient pollution and store large amounts of ‘blue carbon’ in their soils, however, the value of sequestered carbon may be partially offset by nitrous oxide (N₂O) emissions. Global climate and land use changes result in higher temperatures and inputs of reactive nitrogen (Nr) into coastal zones. Here, we investigated the combined effects of elevated temperature (ambient + 5℃) and Nr (double ambient concentrations) on nitrogen processing in marsh soils from two climatic regions (Quebec, Canada and Louisiana, U.S.) with two vegetation types,Sporobolus alterniflorus(= Spartina alterniflora) andSporobolus pumilus(= Spartina patens), using 24-h laboratory incubation experiments. Potential N₂O fluxes increased from minor sinks to major sources following elevated treatments across all four marsh sites. One day of potential N₂O emissions under elevated treatments (representing either long-term sea surface warming or short-term ocean heatwaves effects on coastal marsh soil temperatures alongside pulses of N loading) offset 15–60% of the potential annual ambient N₂O sink, depending on marsh site and vegetation type. Rates of potential denitrification were generally higher in high latitude than in low latitude marsh soils under ambient treatments, with low ratios of N₂O:N₂indicating complete denitrification in high latitude marsh soils. Under elevated temperature and Nr treatments, potential denitrification was lower in high latitude soil but higher in low latitude soil as compared to ambient conditions, with incomplete denitrification observed except in LouisianaS. pumilus. Overall, our findings suggest that a combined increase in temperature and Nr has the potential to reduce salt marsh greenhouse gas (GHG) sinks under future global change scenarios. 

Increasing the capacity of biological nitrogen fixation (BNF) is an effective strategy to enhance food security while simultaneously reducing the carbon and nitrogen footprint of agriculture. Nanotechnology offers several pathways to enhance BNF successfully. 

In this paper, we demonstrate the suitability, sensitivity, and precision of low‐cost and easy‐to‐use ion‐selective electrodes (ISEs) for concurrent detection of NH4+ and NO3‐ in soil and water by technical and non‐technical end‐users to enable efficient soil and water management exposed to chronic reactive nitrogen loading. We developed a simplified methodology for sample preparation followed by the demonstration of an analytical methodology resulting in improvements of sensitivity and precision of ISEs. Herein, we compared and contrasted ISEs with traditional laboratory‐based technique such as Flow Injection Analysis (FIA) and portable colorimetric assay followed by comparisons of linear regression and Bayesian nonlinear calibration approaches applied on both direct potentiometry and standard addition modes of analysis in terms of in‐field applications and improvement of sensitivity and precision. The ISEs were validated for sensing on a range of ambient soil and water samples representing a range of NH4+ and NO3‐ concentrations from pristine to excessive saturation conditions. Herein developed methodology showed excellent agreement with lab‐based and portable analytical techniques while demonstrating improvements in precision and sensitivity analysis illustrated by a decrease in confidence intervals by 50‐60%. We also demonstrated the utilization of the entire ISE response curve thus removing the biases originating from linear approximation which is often currently employed. Therefore, we show that ISEs are robust yet low cost and an easy to use technology that can enable high‐frequency measurement of mineral N and help to improve our understanding of N transformation processes as influenced by soil management, fertilization, land use, and climate change.