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1. Inorganic Nitrogen Gas‐Aerosol Partitioning in and Around Animal Feeding Operations in Northeastern Colorado in Late Summer 2021

   https://doi.org/10.1029/2023JD040507  

   Li, En; Pierce, Jeffrey_R; Juncosa_Calahorrano, Julieta_F; Sullivan, Amy_P; Pollack, Ilana_B; Roscioli, Joseph_R; Caulton, Dana_R; McCabe, Megan_E; Jathar, Shantanu_H; Fischer, Emily_V (June 2024, Journal of Geophysical Research: Atmospheres)

   Abstract Ammonia (NH₃) from animal feeding operations (AFOs) is an important source of reactive nitrogen in the US, but despite its ramifications for air quality and ecosystem health, its near‐source evolution remains understudied. To this end, Phase I of the Transport and Transformation of Ammonia (TRANS²Am) field campaign was conducted in the northeastern Colorado Front Range in summer 2021 and characterized atmospheric composition downwind of AFOs during 10 research flights. Airborne measurements of NH₃, nitric acid (HNO₃), and a suite of water‐soluble aerosol species collected onboard the University of Wyoming King Air research aircraft present an opportunity to investigate the sensitivity of particulate matter (PM) formation to AFO emissions. We couple the observations with thermodynamic modeling to predict the seasonality of ammonium nitrate (NH₄NO₃) formation. We find that during TRANS²Am northeastern Colorado is consistently in the NH₃‐rich and HNO₃‐limited NH₄NO₃formation regime. Further investigation using the Extended Aerosol Inorganics Model reveals that summertime temperatures (mean: 23°C) of northeastern Colorado, especially near the surface, inhibit NH₄NO₃formation despite high NH₃concentrations (max: ≤114 ppbv). Finally, we model spring/autumn and winter conditions to explore the seasonality of NH₄NO₃formation and find that cooler temperatures could support substantially more NH₄NO₃formation. Whereas NH₄NO₃only exceeds 1 μg m⁻³∼10% of the time in summer, modeled NH₄NO₃would exceed 1 μg m⁻³61% (88%) of the time in spring/autumn (winter), with a 10°C (20°C) temperature decrease relative to the campaign. 

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2. Urban aerosol chemistry at a land-water transition site during summer – Part 1: Impact of agricultural and industrial ammonia emissions

   Balasus, N. (January 2021, Atmospheric chemistry and physics discussion)

   null (Ed.)

   This study characterizes the impact of the Chesapeake Bay and associated meteorological phenomena on aerosol chemistry during the second Ozone Water-Land Environmental Transition Study (OWLETS-2) field campaign during summer 2018. Measurements of inorganic PM2.5 composition, gas-phase ammonia (NH3), and an array of meteorological parameters were undertaken at Hart-Miller Island (HMI), a land-water transition site just east of downtown Baltimore on the Chesapeake Bay. The observations at HMI were characterized by abnormally high NH3 concentrations (maximum of 19.3 μg m-3, average of 3.83 μg m-3), which were more than a factor of three higher than NH3 levels measured at the closest Atmospheric Ammonia Network (AMoN) site (approximately 45 km away). While sulfate concentrations at HMI agreed quite well with those measured at a regulatory monitoring station 45 km away, aerosol ammonium and nitrate concentrations were significantly higher, due to the ammonia-rich conditions that resulted from the elevated NH3. The high NH3 concentrations were largely due to regional agricultural emissions, including dairy farms in southeastern Pennsylvania and poultry operations in the Delmarva Peninsula (Delaware-Maryland-Virginia). Reduced NH3 deposition during transport over the Chesapeake Bay likely contributed to enhanced concentrations at HMI compared to the more inland AMoN site. Several peak NH3 events were recorded, including the maximum NH3 observed during OWLETS-2, that appear to originate from a cluster of industrial sources near downtown Baltimore. Such events were all associated with nighttime emissions and advection to HMI under low 15 wind speeds (< 1 m s-1) and stable atmospheric conditions. Our results demonstrate the importance of industrial sources, including several that are not represented in the emissions inventory, on urban air quality. Together with our companion paper, which examines aerosol liquid water and pH during OWLETS-2, we highlight unique processes affecting urban air quality of coastal cities that are distinct from continental locations. 

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3. Surface Ocean Biogeochemistry Regulates the Impact of Anthropogenic Aerosol Fe Deposition on the Cycling of Iron and Iron Isotopes in the North Pacific

   https://doi.org/10.1029/2022GL098016  

   König, D.; Conway, T. M.; Hamilton, D. S.; Tagliabue, A. (July 2022, Geophysical Research Letters)

   Abstract Distinctively‐light isotopic signatures associated with Fe released from anthropogenic activity have been used to trace basin‐scale impacts. However, this approach is complicated by the way Fe cycle processes modulate oceanic dissolved Fe (dFe) signatures (δ⁵⁶Fe_diss) post deposition. Here we include dust, wildfire, and anthropogenic aerosol Fe deposition in a global ocean biogeochemical model with active Fe isotope cycling, to quantify how anthropogenic Fe impacts surface ocean dFe and δ⁵⁶Fe_diss. Using the North Pacific as a natural laboratory, the response of dFe, δ⁵⁶Fe_diss, and primary productivity are spatially and seasonally variable and do not simply follow the footprint of atmospheric deposition. Instead, the effect of anthropogenic Fe is regulated by the biogeochemical regime, specifically the degree of Fe limitation and rates of primary production. Overall, we find that while δ⁵⁶Fe_dissdoes trace anthropogenic input, the response is muted by fractionation during phytoplankton uptake, but amplified by other isotopically‐light Fe sources. 

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4. Rainwater isotopes in central Vietnam controlled by two oceanic moisture sources and rainout effects

   https://doi.org/10.1038/s41598-020-73508-z  

   Wolf, Annabel; Roberts, William H.; Ersek, Vasile; Johnson, Kathleen R.; Griffiths, Michael L. (December 2020, Scientific Reports)

   Abstract The interpretation of palaeoclimate archives based on oxygen isotopes depends critically on a detailed understanding of processes controlling the isotopic composition of precipitation. In the summer monsoonal realm, like Southeast Asia, seasonally and interannually depleted oxygen isotope ratios in precipitation have been linked to the summer monsoon strength. However, in some regions, such as central Vietnam, the majority of precipitation falls outside the summer monsoon period. We investigate processes controlling stable isotopes in precipitation from central Vietnam by combining moisture uptake calculations with monthly stable isotope data observed over five years. We find that the isotopic seasonal cycle in this region is driven by a shift in moisture source from the Indian Ocean to the South China Sea. This shift is reflected in oxygen isotope ratios with low values (− 8 to − 10‰) during summer and high values during spring/winter (0 to − 3‰), while 70% of the annual rainfall occurs during autumn. Interannual changes in precipitation isotopes in central Vietnam are governed by the timing of the seasonal onset and withdrawal of the Intertropical Convergence Zone, which controls the amount of vapour contributed from each source. 

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5. Submarine groundwater discharge as a major nutrient source in river‐fed vs. tidally dominated estuaries

   https://doi.org/10.1002/lno.12772  

   Wilson, Stephanie J; Tamborski, Joseph J; Song, Bongkeun; Bernhardt, Peter; Mulholland, Margaret R (February 2025, Limnology and Oceanography)

   Abstract The tidal tributaries of the lower Chesapeake Bay experience seasonally recurring harmful algal blooms and the significance of submarine groundwater discharge (SGD) as a nutrient vector is largely unknown. Here, we determined seasonal SGD nutrient loads in two tributaries with contrasting hydrodynamic conditions, river‐fed (York River) vs. tidally dominated (Lafayette River). Radon surveys were performed in each river to quantify SGD at the embayment‐scale during spring and fall 2021. Total SGD was determined from a²²²Rn mass balance and Monte Carlo simulations. Submarine groundwater discharge rates differed by a factor of two during spring (Lafayette = 11 ± 17 cm d⁻¹; York = 6 ± 10 cm d⁻¹) and a factor of six during fall (Lafayette = 19 ± 27 cm d⁻¹; York = 3 ± 7 cm d⁻¹). Groundwater N concentrations and fluxes varied seasonally in the York (4–7 mmol N m⁻²d⁻¹). In the Lafayette River, seasonal N fluxes (22–37 mmol N m⁻²d⁻¹) were driven by seasonal water exchange rates, likely due to recurrent saltwater intrusion. Submarine groundwater discharge–derived nutrient fluxes were orders of magnitude greater than riverine inputs and runoff in each system. Additionally, sediment N removal by denitrification and anaerobic ammonium oxidation would only remove ~ 1–11% of dissolved inorganic nitrogen supplied through SGD. The continued recurrence of harmful algal blooms in the Bay's tidal tributaries may be indicative of an under‐accounting of submarine groundwater‐borne nutrient sources. This study highlights the importance of including SGD in water quality models used to advise restoration efforts in the Chesapeake Bay region and beyond. 

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