Significance: In lakes, chloride is a relatively benign ion at low concentrations but begins to have ecological impacts as concentrations rise into the 100s and 1,000s of mg L ⁻¹ . In this study, we investigate long-term chloride trends in 371 freshwater lakes in North America. We find that in Midwest and Northeast North America, most urban lakes and rural lakes that are surrounded by >1% impervious land cover show increasing chloride trends. Expanding on this finding, thousands of lakes in these regions are at risk of long-term salinization. Keeping lakes “fresh” is critically important for protecting the ecosystem services freshwater lakes provide, such as drinking water, fisheries, recreation, irrigation, and aquatic habitat.

Methane (CH₄) emissions from natural landscapes constitute roughly half of global CH₄ contributions to the atmosphere, yet large uncertainties remain in the absolute magnitude and the seasonality of emission quantities and drivers. Eddy covariance (EC) measurements of CH₄ flux are ideal for constraining ecosystem-scale CH₄ emissions due to quasi-continuous and high-temporal-resolution CH₄ flux measurements, coincident carbon dioxide, water, and energy flux measurements, lack of ecosystem disturbance, and increased availability of datasets over the last decade. Here, we (1) describe the newly published dataset, FLUXNET-CH₄ Version 1.0, the first open-source global dataset of CH₄ EC measurements (available at https://fluxnet.org/data/fluxnet-ch4-community-product/, last access: 7 April 2021). FLUXNET-CH₄ includes half-hourly and daily gap-filled and non-gap-filled aggregated CH₄ fluxes and meteorological data from 79 sites globally: 42 freshwater wetlands, 6 brackish and saline wetlands, 7 formerly drained ecosystems, 7 rice paddy sites, 2 lakes, and 15 uplands. Then, we (2) evaluate FLUXNET-CH₄ representativeness for freshwater wetland coverage globally because the majority of sites in FLUXNET-CH₄ Version 1.0 are freshwater wetlands which are a substantial source of total atmospheric CH₄ emissions; and (3) we provide the first global estimates of the seasonal variability and seasonality predictors of freshwater wetland CH₄ fluxes. Our representativeness analysis suggests that the freshwater wetland sites in the dataset cover global wetland bioclimatic attributes (encompassing energy, moisture, and vegetation-related parameters) in arctic, boreal, and temperate regions but only sparsely cover humid tropical regions. Seasonality metrics of wetland CH₄ emissions vary considerably across latitudinal bands. In freshwater wetlands (except those between 20^∘ S to 20^∘ N) the spring onset of elevated CH₄ emissions starts 3 d earlier, and the CH₄ emission season lasts 4 d longer, for each degree Celsius increase in mean annual air temperature. On average, the spring onset of increasing CH₄ emissions lags behind soil warming by 1 month, with very few sites experiencing increased CH₄ emissions prior to the onset of soil warming. In contrast, roughly half of these sites experience the spring onset of rising CH₄ emissions prior to the spring increase in gross primary productivity (GPP). The timing of peak summer CH₄ emissions does not correlate with the timing for either peak summer temperature or peak GPP. Our results provide seasonality parameters for CH₄ modeling and highlight seasonality metrics that cannot be predicted by temperature or GPP (i.e., seasonality of CH₄ peak). FLUXNET-CH₄ is a powerful new resource for diagnosing and understanding the role of terrestrial ecosystems and climate drivers in the global CH₄ cycle, and future additions of sites in tropical ecosystems and site years of data collection will provide added value to this database. All seasonality parameters are available at https://doi.org/10.5281/zenodo.4672601 (Delwiche et al., 2021). Additionally, raw FLUXNET-CH₄ data used to extract seasonality parameters can be downloaded from https://fluxnet.org/data/fluxnet-ch4-community-product/ (last access: 7 April 2021), and a complete list of the 79 individual site data DOIs is provided in Table 2 of this paper.

Natural gas stoves in >40 million U.S. residences release methane (CH₄)─a potent greenhouse gas─through post-meter leaks and incomplete combustion. We quantified methane released in 53 homes during all phases of stove use: steady-state-off (appliance not in use), steady-state-on (during combustion), and transitory periods of ignition and extinguishment. We estimated that natural gas stoves emit 0.8–1.3% of the gas they use as unburned methane and that total U.S. stove emissions are 28.1 [95% confidence interval: 18.5, 41.2] Gg CH₄ year^–1. More than three-quarters of methane emissions we measured originated during steady-state-off. Using a 20-year timeframe for methane, annual methane emissions from all gas stoves in U.S. homes have a climate impact comparable to the annual carbon dioxide emissions of 500 000 cars. In addition to methane emissions, co-emitted health-damaging air pollutants such as nitrogen oxides (NO_x) are released into home air and can trigger respiratory diseases. In 32 homes, we measured NO_x (NO and NO₂) emissions and found them to be linearly related to the amount of natural gas burned (r² = 0.76; p ≪ 0.01). Emissions averaged 21.7 [20.5, 22.9] ng NO_x J^–1, comprised of 7.8 [7.1, 8.4] ng NO₂ J^–1 and 14.0 [12.8, 15.1] ng NO J^–1. Our data suggest that families who don’t use their range hoods or who have poor ventilation can surpass the 1-h national standard of NO₂ (100 ppb) within a few minutes of stove usage, particularly in smaller kitchens.