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Abstract Concentrations of total dissolved inorganic carbon (DIC) in freshwater ecosystems are controlled by terrestrial inputs and a myriad of in situ processes, such as aquatic metabolism. Dissolved CO₂is one of the components of DIC, and its dynamics are also regulated by chemical equilibrium with the DIC pool, so‐called carbonate buffering. Although its importance is generally recognized, carbonate buffering is still not consistently accounted for in freshwater studies. Here, we review key concepts in freshwater carbonate buffering, perform simulation experiments, and provide a case study of an alkaline river to illustrate calculations of DIC from CO₂. These analyses demonstrate that carbonate buffering can alter common interpretations of CO₂data, including carbon–oxygen coupling through production and respiration. As direct measurements of dissolved CO₂are increasingly common, accounting for CO₂equilibria with DIC is critical to understanding its role in carbon cycling within most freshwater systems. 

Stream metabolism, encompassing gross primary production and ecosystem respiration, reflects the fundamental energetic dynamics of freshwater ecosystems. These processes regulate the concentrations of dissolved gases like oxygen and carbon dioxide, which in turn shape aquatic food webs and ecosystem responses to stressors such as floods, drought, and nutrient loading. Historically difficult to quantify, stream metabolism is now measurable at high temporal resolution thanks to advances in sensor technology and modeling. The StreamPULSE dataset includes high-frequency sensor data, metadata, and modeled estimates of ecosystem metabolism. This living dataset contributes to a growing body of open-access data characterizing the metabolic pulse of stream ecosystems worldwide. To contribute to StreamPULSE, visit data.streampulse.org. All data contributed to StreamPULSE become public after an optional embargo period. Use this publication to access annual data releases, or use data.streampulse.org to download new data as they become available. 

Abstract Rivers efficiently collect, process, and transport terrestrial‐derived carbon. River ecosystem metabolism is the primary mechanism for processing carbon. Diel cycles of dissolved oxygen (DO) have been used for decades to infer river ecosystem metabolic rates, which are routinely used to predict metabolism of carbon dioxide (CO₂) with uncertainties of the assumed stoichiometry ranging by a factor of 4. Dissolved inorganic carbon (DIC) has been less used to directly infer metabolism because it is more difficult to quantify, involves the complexity of inorganic carbon speciation, and as shown in this study, likely requires a two‐station approach. Here, we developed DIC metabolism models using single‐ and two‐station approaches. We compared metabolism estimates based on simultaneous DO and DIC monitoring in the Upper Clark Fork River (USA), which also allowed us to estimate ecosystem‐level photosynthetic and respiratory quotients (PQ_Eand RQ_E). We observed that metabolism estimates from DIC varied more between single‐ and two‐station approaches than estimates from DO. Due to carbonate buffering, CO₂is slower to equilibrate with the atmosphere compared to DO, likely incorporating a longer distance of upstream heterogeneity. Reach‐averaged PQ_Eranged from 1.5 to 2.0, while RQ_Eranged from 0.8 to 1.5. Gross primary production from DO was larger than that from DIC, as was net ecosystem production by . The river was autotrophic based on DO but heterotrophic based on DIC, complicating our understanding of how metabolism regulated CO₂production. We suggest future studies simultaneously model metabolism from DO and DIC to understand carbon processing in rivers. 

This dataset contains estimates of gas exchange velocity, gas exchange rate, and hydraulic parameters for streams calculated from tracer-gas experiments and conservative tracer injections collected by the National Ecological Observatory Network (NEON). All input data were collected by NEON and is available on the NEON data portal at https://data.neonscience.org. Specifically, the NEON Reaeration field and lab collection data product (DP1.20190.001) was used to calculate these estimates. Gas exchange was estimated in two ways: first, following an unpooled frequentist approach and second, following a partially pooled Bayesian approach. In addition, a salt-correction was applied to gas exchange estimates for sites where it was possible and necessary. All estimates of gas exchange are included in the file gasExchange_ds.csv. A recommended selection of these estimates is included in the dataset (best_k600_mPerDay and best_K600_mPerDay). The stanfit objects used for the partially pooled Bayesian approach are also included as site-specific model objects for gas exchange velocities and rates. In addition, water velocity was calculated from conservative tracer injections, and mean water depth was calculated from these water velocity estimates and measurements of wetted width and water discharge. All hydraulic parameters are included in the file hydraulics_ds.csv. All processing code is available in the reaRates R package. NEON is sponsored by the National Science Foundation (NSF) and operated under cooperative agreement by Battelle. This material is based in part upon work supported by NSF through the NEON Program. 

Knowledge gaps about how the ocean melts Antarctica’s ice shelves, borne from a lack of observations, lead to large uncertainties in sea level predictions. Using high-resolution maps of the underside of Dotson Ice Shelf, West Antarctica, we reveal the imprint that ice shelf basal melting leaves on the ice. Convection and intermittent warm water intrusions form widespread terraced features through slow melting in quiescent areas, while shear-driven turbulence rapidly melts smooth, eroded topographies in outflow areas, as well as enigmatic teardrop-shaped indentations that result from boundary-layer flow rotation. Full-thickness ice fractures, with bases modified by basal melting and convective processes, are observed throughout the area. This new wealth of processes, all active under a single ice shelf, must be considered to accurately predict future Antarctic ice shelf melt. 

Considerable attention is given to absolute nutrient levels in lakes, rivers, and oceans, but less is paid to their relative concentrations, their nitrogen:phosphorus (N:P) stoichiometry, and the consequences of imbalanced stoichiometry. Here, we report 38 y of nutrient dynamics in Flathead Lake, a large oligotrophic lake in Montana, and its inflows. While nutrient levels were low, the lake had sustained high total N: total P ratios (TN:TP: 60 to 90:1 molar) throughout the observation period. N and P loading to the lake as well as loading N:P ratios varied considerably among years but showed no systematic long-term trend. Surprisingly, TN:TP ratios in river inflows were consistently lower than in the lake, suggesting that forms of P in riverine loading are removed preferentially to N. In-lake processes, such as differential sedimentation of P relative to N or accumulation of fixed N in excess of denitrification, likely also operate to maintain the lake’s high TN:TP ratios. Regardless of causes, the lake’s stoichiometric imbalance is manifested in P limitation of phytoplankton growth during early and midsummer, resulting in high C:P and N:P ratios in suspended particulate matter that propagate P limitation to zooplankton. Finally, the lake’s imbalanced N:P stoichiometry appears to raise the potential for aerobic methane production via metabolism of phosphonate compounds by P-limited microbes. These data highlight the importance of not only absolute N and P levels in aquatic ecosystems, but also their stoichiometric balance, and they call attention to potential management implications of high N:P ratios.