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Methane is a powerful greenhouse gas and a key player in atmospheric chemistry. Important uncertainties remain in the global atmospheric methane budget, with natural geologic emissions being one of the particularly uncertain terms. In recent bottom-up studies, geologic emissions have been estimated to comprise up to 10% of the global budget (40–60 Teragrams of methane per year, Tg CH4 yr–1). In contrast, top-down constraints from 14C of methane in preindustrial air extracted from ice cores indicate that the geologic methane source is approximately an order of magnitude lower. Recent bottom-up inventories propose microseepage (diffuse low-level flux of methane through soils over large areas) as the largest single component of the geologic methane flux. In this study, we present new measurements of methane microseepage from the Appalachian Basin (Western New York State) and compare these with prior microseepage measurements from other regions and with predicted values from the most recent bottom-up inventory. Our results show lower microseepage values than most prior data sets and indicate that positive microseepage fluxes in this region are not as widespread as previously assumed. A statistical analysis of our results indicates that mean microseepage flux in this region has very likely been overestimated by the bottom-up inventory, even though our measurements more likely than not underestimate the true mean flux. However, this is a small data set from a single region and as such cannot be used to evaluate the validity of the microseepage emissions inventory as a whole. Instead, the results demonstrate the need for a more extensive network of direct geologic emission measurements in support of improved bottom-up inventories. 

Assessment of the global budget of the greenhouse gas nitrous oxide (${\mathrm{N}}_2$O) is limited by poor knowledge of the oceanic${\mathrm{N}}_2$O flux to the atmosphere, of which the magnitude, spatial distribution, and temporal variability remain highly uncertain. Here, we reconstruct climatological${\mathrm{N}}_2$O emissions from the ocean by training a supervised learning algorithm with over 158,000${\mathrm{N}}_2$O measurements from the surface ocean—the largest synthesis to date. The reconstruction captures observed latitudinal gradients and coastal hot spots of${\mathrm{N}}_2$O flux and reveals a vigorous global seasonal cycle. We estimate an annual mean${\mathrm{N}}_2$O flux of 4.2 ± 1.0 Tg N$\cdot {\mathrm{y}}^{-1}$, 64% of which occurs in the tropics, and 20% in coastal upwelling systems that occupy less than 3% of the ocean area. This${\mathrm{N}}_2$O flux ranges from a low of 3.3 ± 1.3 Tg N$\cdot {\mathrm{y}}^{-1}$in the boreal spring to a high of 5.5 ± 2.0 Tg N$\cdot {\mathrm{y}}^{-1}$in the boreal summer. Much of the seasonal variations in global${\mathrm{N}}_2$O emissions can be traced to seasonal upwelling in the tropical ocean and winter mixing in the Southern Ocean. The dominant contribution to seasonality by productive, low-oxygen tropical upwelling systems (>75%) suggests a sensitivity of the global${\mathrm{N}}_2$O flux to El Niño–Southern Oscillation and anthropogenic stratification of the low latitude ocean. This ocean flux estimate is consistent with the range adopted by the Intergovernmental Panel on Climate Change, but reduces its uncertainty by more than fivefold, enabling more precise determination of other terms in the atmospheric${\mathrm{N}}_2$O budget.

 

Models and observations suggest that particle flux attenuation is lower across the mesopelagic zone of anoxic environments compared to oxic environments. Flux attenuation is controlled by microbial metabolism as well as aggregation and disaggregation by zooplankton, all of which shape the relative abundance of differently sized particles. Observing and modeling particle spectra can provide information about the contributions of these processes. We measured particle size spectrum profiles at one station in the oligotrophic Eastern Tropical North Pacific Oxygen Deficient Zone (ETNP ODZ) using an underwater vision profiler (UVP), a high‐resolution camera that counts and sizes particles. Measurements were taken at different times of day, over the course of a week. Comparing these data to particle flux measurements from sediment traps collected over the same time‐period allowed us to constrain the particle size to flux relationship, and to generate highly resolved depth and time estimates of particle flux rates. We found that particle flux attenuated very little throughout the anoxic water column, and at some time points appeared to increase. Comparing our observations to model predictions suggested that particles of all sizes remineralize more slowly in the ODZ than in oxic waters, and that large particles disaggregate into smaller particles, primarily between the base of the photic zone and 500 m. Acoustic measurements of multiple size classes of organisms suggested that many organisms migrated, during the day, to the region with high particle disaggregation. Our data suggest that diel‐migrating organisms both actively transport biomass and disaggregate particles in the ODZ core.

 

Abstract. In the current era of rapid climate change, accuratecharacterization of climate-relevant gas dynamics – namely production,consumption, and net emissions – is required for all biomes, especially thoseecosystems most susceptible to the impact of change. Marine environmentsinclude regions that act as net sources or sinks for numerous climate-activetrace gases including methane (CH4) and nitrous oxide (N2O). Thetemporal and spatial distributions of CH4 and N2O are controlledby the interaction of complex biogeochemical and physical processes. Toevaluate and quantify how these mechanisms affect marine CH4 andN2O cycling requires a combination of traditional scientificdisciplines including oceanography, microbiology, and numerical modeling.Fundamental to these efforts is ensuring that the datasets produced byindependent scientists are comparable and interoperable. Equally critical istransparent communication within the research community about the technicalimprovements required to increase our collective understanding of marineCH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB)was organized to enhance dialogue and collaborations pertaining tomarine CH4 and N2O. Here, we summarize the outcomes from theworkshop to describe the challenges and opportunities for near-futureCH4 and N2O research in the marine environment.