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Determining the magnitude and origins of nitrogen (N) deposition in the open ocean is vital for understanding how anthropogenic activities influence oceanic biogeochemical cycles. Excess N in the North Pacific Ocean(NPO) is suggested to reflect recent anthropogenic atmospheric deposition from the Asian continent, changes in nutrient dynamics due to marine N-fixation, and/or lateral transport of nutrients. We investigate the impact of anthropogenic and marine sources on reactive N deposition in the NPO, with a focus on ammonium (NH4+), an important bioavailable nutrient, using aerosol samples (n =108) collected off the coast of China (Changdao Island). This study site is used as a proxy for continental emissions that can be exported and subsequently deposited to the ocean. The NH4+concentration of aerosol samples varied seasonally (p < 0.05), with a higher average value in winter (2.8 ±1.1 μg/m3) and spring (1.9 ±0.8 μg/m3) compared to autumn (0.7 ±0.6 μg/m3) and summer (1.4 ±0.4 μg/m3). The isotopic composition of aerosol NH4+ varied seasonally, with higher averages in spring (13.3 ±7.9‰) and summer (15.6 ±6.2‰) compared to autumn (3.2 ±2.5 ‰) and winter (3.8 ±11.4‰). These seasonal patterns in the isotopic composition of NH4+ are investigated based on correlations of aerosol chemical species, seasonal shifts in transport patterns, partitioning of ammonia/ammonium between the gas and particle phase, and continental versus marine sources of ammonia. We find that anthropogenic activities, mainly agricultural practices (e.g., volatilization, fertilizer, animal husbandry), are the primary sources of NH4+ deposited to the NPO. 

Aerosols and clouds are key components of the marine atmosphere, impacting the Earth’s radiative budget with a net cooling effect over the industrial era that counterbalances greenhouse gas warming, yet with an uncertain amplitude. Here we report recent advances in our understanding of how open ocean aerosol sources are modulated by ocean biogeochemistry and how they, in turn, shape cloud coverage and properties. We organize these findings in successive steps from ocean biogeochemical processes to particle formation by nucleation and sea spray emissions, further particle growth by condensation of gases, the potential to act as cloud condensation nuclei or ice nucleating particles, and finally, their effects on cloud formation, optical properties, and life cycle. We discuss how these processes may be impacted in a warming climate and the potential for ocean biogeochemistry—climate feedbacks through aerosols and clouds. 

This commentary paper from the recently formed International Global Atmospheric Chemistry (IGAC) Southern Hemisphere Working Group outlines key issues in atmospheric composition research that particularly impact the Southern Hemisphere. In this article, we present a broad overview of many of the challenges for understanding atmospheric chemistry in the Southern Hemisphere, before focusing in on the most significant factors that differentiate it from the Northern Hemisphere. We present sections on the importance of biogenic emissions and fires in the Southern Hemisphere, showing that these emissions often dominate over anthropogenic emissions in many regions. We then describe how these and other factors influence air quality in different parts of the Southern Hemisphere. Finally, we describe the key role of the Southern Ocean in influencing atmospheric chemistry and conclude with a description of the aims and scope of the newly formed IGAC Southern Hemisphere Working Group.