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Dimethyl sulfide (DMS), emitted from the oceans, is the most abundant biological source of sulfur to the marine atmosphere. Atmospheric DMS is oxidized to condensable products that form secondary aerosols that affect Earth’s radiative balance by scattering solar radiation and serving as cloud condensation nuclei. We report the atmospheric discovery of a previously unquantified DMS oxidation product, hydroperoxymethyl thioformate (HPMTF, HOOCH₂SCHO), identified through global-scale airborne observations that demonstrate it to be a major reservoir of marine sulfur. Observationally constrained model results show that more than 30% of oceanic DMS emitted to the atmosphere forms HPMTF. Coincident particle measurements suggest a strong link between HPMTF concentration and new particle formation and growth. Analyses of these observations show that HPMTF chemistry must be included in atmospheric models to improve representation of key linkages between the biogeochemistry of the ocean, marine aerosol formation and growth, and their combined effects on climate.

CH 4 is the most abundant reactive greenhouse gas and a complete understanding of its atmospheric fate is needed to formulate mitigation policies. Current chemistry-climate models tend to underestimate the lifetime of CH 4 , suggesting uncertainties in its sources and sinks. Reactive halogens substantially perturb the budget of tropospheric OH, the main CH 4 loss. However, such an effect of atmospheric halogens is not considered in existing climate projections of CH 4 burden and radiative forcing. Here, we demonstrate that reactive halogen chemistry increases the global CH 4 lifetime by 6–9% during the 21st century. This effect arises from significant halogen-mediated decrease, mainly by iodine and bromine, in OH-driven CH 4 loss that surpasses the direct Cl-induced CH 4 sink. This increase in CH 4 lifetime helps to reduce the gap between models and observations and results in a greater burden and radiative forcing during this century. The increase in CH 4 burden due to halogens (up to 700 Tg or 8% by 2100) is equivalent to the observed atmospheric CH 4 growth during the last three to four decades. Notably, the halogen-driven enhancement in CH 4 radiative forcing is 0.05 W/m 2 at present and is projected to increase in the future (0.06 W/m 2 by 2100); such enhancement equals ~10% of present-day CH 4 radiative forcing and one-third of N 2 O radiative forcing, the third-largest well-mixed greenhouse gas. Both direct (Cl-driven) and indirect (via OH) impacts of halogens should be included in future CH 4 projections. Methane is a powerful greenhouse gas and previous studies focus on its sources with less attention on the loss. Here the authors show that reactive halogen species, not considered in climate projections, significantly reduces the methane loss, increasing its lifetime, burden, and radiative forcing.

Aerosol indirect radiative forcing (IRF), which characterizes how aerosols alter cloud formation and properties, is very sensitive to the preindustrial (PI) aerosol burden. Dimethyl sulfide (DMS), emitted from the ocean, is a dominant natural precursor of non-sea-salt sulfate in the PI and pristine present-day (PD) atmospheres. Here we revisit the atmospheric oxidation chemistry of DMS, particularly under pristine conditions, and its impact on aerosol IRF. Based on previous laboratory studies, we expand the simplified DMS oxidation scheme used in the Community Atmospheric Model version 6 with chemistry (CAM6-chem) to capture the OH-addition pathway and the H-abstraction pathway and the associated isomerization branch. These additional oxidation channels of DMS produce several stable intermediate compounds, e.g., methanesulfonic acid (MSA) and hydroperoxymethyl thioformate (HPMTF), delay the formation of sulfate, and, hence, alter the spatial distribution of sulfate aerosol and radiative impacts. The expanded scheme improves the agreement between modeled and observed concentrations of DMS, MSA, HPMTF, and sulfate over most marine regions, based on the NASA Atmospheric Tomography (ATom), the Aerosol and Cloud Experiments in the Eastern North Atlantic (ACE-ENA), and the Variability of the American Monsoon Systems (VAMOS) Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx) measurements. We find that the global HPMTF burden and the burden of sulfate produced from DMS oxidation are relatively insensitive to the assumed isomerization rate, but the burden of HPMTF is very sensitive to a potential additional cloud loss. We find that global sulfate burden under PI and PD emissions increase to 412 Gg S (+29 %) and 582 Gg S (+8.8 %), respectively, compared to the standard simplified DMS oxidation scheme. The resulting annual mean global PD direct radiative effect of DMS-derived sulfate alone is −0.11 W m−2. The enhanced PI sulfate produced via the gas-phase chemistry updates alone dampens the aerosol IRF as anticipated (−2.2 W m−2 in standard versus −1.7 W m−2, with updated gas-phase chemistry). However, high clouds in the tropics and low clouds in the Southern Ocean appear particularly sensitive to the additional aqueous-phase pathways, counteracting this change (−2.3 W m−2). This study confirms the sensitivity of aerosol IRF to the PI aerosol loading and the need to better understand the processes controlling aerosol formation in the PI atmosphere and the cloud response to these changes.

Ozone is the third most important anthropogenic greenhouse gas after carbon dioxide and methane but has a larger uncertainty in its radiative forcing, in part because of uncertainty in the source characteristics of ozone precursors, nitrogen oxides, and volatile organic carbon that directly affect ozone formation chemistry. Tropospheric ozone also negatively affects human and ecosystem health. Biomass burning (BB) and urban emissions are significant but uncertain sources of ozone precursors. Here, we report global-scale, in situ airborne measurements of ozone and precursor source tracers from the NASA Atmospheric Tomography mission. Measurements from the remote troposphere showed that tropospheric ozone is regularly enhanced above background in polluted air masses in all regions of the globe. Ozone enhancements in air with high BB and urban emission tracers (2.1 to 23.8 ppbv [parts per billion by volume]) were generally similar to those in BB-influenced air (2.2 to 21.0 ppbv) but larger than those in urban-influenced air (−7.7 to 6.9 ppbv). Ozone attributed to BB was 2 to 10 times higher than that from urban sources in the Southern Hemisphere and the tropical Atlantic and roughly equal to that from urban sources in the Northern Hemisphere and the tropical Pacific. Three independent global chemical transport models systematically underpredict the observed influence of BB on tropospheric ozone. Potential reasons include uncertainties in modeled BB injection heights and emission inventories, export efficiency of BB emissions to the free troposphere, and chemical mechanisms of ozone production in smoke. Accurately accounting for intermittent but large and widespread BB emissions is required to understand the global tropospheric ozone burden.

Aircraft measurements, laboratory photolysis experiments and modelling calculations reveal a mechanism for the recycling of nitric acid into nitrogen oxides; this enables observations to be reconciled with model studies, and suggests that particulate nitrate photolysis could be a substantial tropospheric nitrogen oxide source. Rapid NO x recycling in marine air Nitrogen oxides play a central role in tropospheric chemistry, but current understanding of the processes responsible for their formation and removal from the atmosphere is insufficient to reconcile model studies with observations. This paper presents aircraft measurements, laboratory photolysis experiments and modelling calculations that reveal a mechanism for the rapid recycling of nitric acid to nitrous acid and nitrogen oxides in the clean marine boundary layer via particulate nitrate photolysis. The authors suggest that this process could be an important tropospheric nitrogen oxide source in remote oceanic regions with implications for tropospheric oxidant and secondary atmospheric aerosol formation. Nitrogen oxides are essential for the formation of secondary atmospheric aerosols and of atmospheric oxidants such as ozone and the hydroxyl radical, which controls the self-cleansing capacity of the atmosphere 1 . Nitric acid, a major oxidation product of nitrogen oxides, has traditionally been considered to be a permanent sink of nitrogen oxides 1 . However, model studies predict higher ratios of nitric acid to nitrogen oxides in the troposphere than are observed 2 , 3 . A ‘renoxification’ process that recycles nitric acid into nitrogen oxides has been proposed to reconcile observations with model studies 2 , 3 , 4 , but the mechanisms responsible for this process remain uncertain 5 , 6 , 7 , 8 , 9 . Here we present data from an aircraft measurement campaign over the North Atlantic Ocean and find evidence for rapid recycling of nitric acid to nitrous acid and nitrogen oxides in the clean marine boundary layer via particulate nitrate photolysis. Laboratory experiments further demonstrate the photolysis of particulate nitrate collected on filters at a rate more than two orders of magnitude greater than that of gaseous nitric acid, with nitrous acid as the main product. Box model calculations based on the Master Chemical Mechanism 10 , 11 suggest that particulate nitrate photolysis mainly sustains the observed levels of nitrous acid and nitrogen oxides at midday under typical marine boundary layer conditions. Given that oceans account for more than 70 per cent of Earth’s surface, we propose that particulate nitrate photolysis could be a substantial tropospheric nitrogen oxide source. Recycling of nitrogen oxides in remote oceanic regions with minimal direct nitrogen oxide emissions could increase the formation of tropospheric oxidants and secondary atmospheric aerosols on a global scale.

External cycling regenerating nitrogen oxides (NO x  ≡ NO + NO 2 ) from their oxidative reservoir, NO z , is proposed to reshape the temporal–spatial distribution of NO x and consequently hydroxyl radical (OH), the most important oxidant in the atmosphere. Here we verify the in situ external cycling of NO x in various environments with nitrous acid (HONO) as an intermediate based on synthesized field evidence collected onboard aircraft platform at daytime. External cycling helps to reconcile stubborn underestimation on observed ratios of HONO/NO 2 and NO 2 /NO z by current chemical model schemes and rationalize atypical diurnal concentration profiles of HONO and NO 2 lacking noontime valleys specially observed in low-NO x atmospheres. Perturbation on the budget of HONO and NO x by external cycling is also found to increase as NO x concentration decreases. Consequently, model underestimation of OH observations by up to 41% in low NO x atmospheres is attributed to the omission of external cycling in models. External cycling regenerates nitrogen oxides from the NO x oxidative reservoir, NO z . Aircraft observations reveal NO x external cycling compensates for NO x aging, sustaining NO x distribution and production of OH radicals far from NO x emission sources

Aircraft observations of the four chloromethanes: carbon tetrachloride (CCl4), methyl chloride (CH3Cl), dichloromethane (CH2Cl2), and chloroform (CHCl3), collected over North America between 2000 and 2022, were used to evaluate their vertical distributions and temporal trends in the atmosphere. We examine the vertical profiles, from the surface to the lower stratosphere (LS), of these increasingly important contributors to ozone‐depleting chlorine in both altitude and potential temperature space. Airborne chloromethane trends were compared with those measured at long‐term, ground‐based monitoring stations. Below 20 km altitude, CCl4 trends were decreasing at all levels studied in the North American atmosphere (−1.1 ppt yr−1). CHCl3 and CH2Cl2 airborne observations were comparable to ground network measurements: CHCl3 increased between 2000 and 2018 and then decreased leading to a negligible trend over the 22 years studied and CH2Cl2 has been increasing at all levels in the troposphere (+2.41 ppt yr−1, 2000–2022, <20 km). Plain Language Summary Atmospheric processes can transport surface emissions of organic chlorine (Cl) compounds to higher altitudes, including the lower stratosphere (LS). At these high altitudes, organic Cl compounds will react, releasing the Cl radical. Subsequent Cl‐radical reactions can lead to the depletion of ozone. The ozone layer surrounds the globe at these high altitudes and is responsible for protecting life on the surface from harmful UV radiation. Therefore, it is important to have data on species containing organic Cl, especially those that are of increasing concern because their sources and sinks are not fully understood. We collect information about four different Cl‐containing species, three of which are not currently regulated by the Montreal Protocol and calculate how their abundances at different altitudes in the atmosphere have changed over 22 years. We use data collected from aircraft flights over North America and ground‐based monitoring sites within America to determine the mixing ratios of these species. Key Points Evaluated chloromethane abundances over North American troposphere and lower stratosphere Collated 22 years of chloromethane measurements collected from airborne platforms Calculated trends from annual means at different atmospheric levels and were comparable to long‐term surface site measurements

Here we use satellite observations of formaldehyde (HCHO) vertical column densities (VCD) from the TROPOspheric Monitoring Instrument (TROPOMI), aircraft measurements, combined with a nested regional chemical transport model (GEOS-Chem at 0.5×0.625∘ resolution), to better understand the variability and sources of summertime HCHO in Alaska. We first evaluate GEOS-Chem with in-situ airborne measurements during the Atmospheric Tomography Mission 1 (ATom-1) aircraft campaign. We show reasonable agreement between observed and modeled HCHO, isoprene, monoterpenes and the sum of methyl vinyl ketone and methacrolein (MVK+MACR) in the continental boundary layer. In particular, HCHO profiles show spatial homogeneity in Alaska, suggesting a minor contribution of biogenic emissions to HCHO VCD. We further examine the TROPOMI HCHO product in Alaska in summer, reprocessed by GEOS-Chem model output for a priori profiles and shape factors. For years with low wildfire activity (e.g., 2018), we find that HCHO VCDs are largely dominated by background HCHO (58 %–71 %), with minor contributions from wildfires (20 %–32 %) and biogenic VOC emissions (8 %–10 %). For years with intense wildfires (e.g., 2019), summertime HCHO VCD is dominated by wildfire emissions (50 %–72 %), with minor contributions from background (22 %–41 %) and biogenic VOCs (6 %–10 %). In particular, the model indicates a major contribution of wildfires from direct emissions of HCHO, instead of secondary production of HCHO from oxidation of larger VOCs. We find that the column contributed by biogenic VOC is often small and below the TROPOMI detection limit, in part due to the slow HCHO production from isoprene oxidation under low NOx conditions. This work highlights challenges for quantifying HCHO and its precursors in remote pristine regions.

Reactive halogens catalytically destroy O3 and therefore affect (1) stratospheric O3 depletion and (2) the oxidative capacity of the troposphere. Reactive halogens also partition into the aerosol phase, but what governs halogen-aerosol partitioning is poorly constrained in models. In this work, we present global-scale measurements of non-sea-salt aerosol (nSSA) bromine and iodine taken during the NASA Atmospheric Tomography Mission (ATom). Using the Particle Analysis by Laser Mass Spectrometry instrument, we found that bromine and iodine are present in 8 %–26 % (interquartile range, IQR) and 12 %–44 % (IQR) of accumulation-mode nSSA, respectively. Despite being commonly found in nSSA, the concentrations of bromine and iodine in nSSA were low but potentially important, at 0.11–0.57 pmol mol−1 (IQR) and 0.04–0.24 pmol mol−1 (IQR), respectively. In the troposphere, we find two distinct sources of bromine and iodine for nSSA: (1) a primary source from biomass burning and (2) a pervasive secondary source. In the stratosphere, nSSA bromine and iodine concentrations increased with increasing O3 concentrations; however, higher concentrations of stratospheric nSSA bromine and iodine were found in organic-rich particles that originated in the troposphere. Finally, we compared our ATom nSSA iodine measurements to the global chemical transport model GEOS-Chem (Goddard Earth Observing System); nSSA bromine concentrations could not be compared because they were not tracked in the model. We found that the model compared well to our ATom nSSA iodine measurements in the background atmosphere but not in the marine boundary layer, biomass burning plumes, or stratosphere.

We present global airborne observations of acetyl peroxynitrate (CH3C(O)OONO2, PAN) in the remote troposphere from the Atmospheric Tomography (ATom) campaign. These observations show that biomass burning is the dominant source of PAN in the Southern Hemisphere (SH). In the Northern Hemisphere, anthropogenic emissions from Asia and Europe also contribute significantly to PAN over the Pacific and Atlantic Oceans. Model simulations underestimate PAN in the lower troposphere, in part, due to the underestimation of local production driven by acetaldehyde oxidation and βNO2 ${\\beta }_{{\\text{NO}}_{2}}$ (the ratio of acetyl peroxy radicals reacting with NO2 relative to other pathways). The significant impacts of biomass burning evident in the ATom PAN observations suggest that improving model treatment of plume transport and the conversion of NOx to PAN in biomass burning plumes is a viable focus for better simulating PAN. Global observations of PAN provide a benchmark for the evaluation of satellite observations and model simulations of PAN.