Comparison of inorganic nitrogen concentrations in airborne particles at inshore and offshore sites in the Yellow Sea (2017-2019): Long-range transport and potential impact on marine productivity.

Atmospheric deposition of nitrogen is one of the most important external nutrient sources. We investigated the concentrations of NO3- and NH4+ in airborne particles at both an offshore and an inshore site in the Yellow Sea. At the offshore site, devoid of local sources and located downwind from the highly developed areas of Korea and China, the concentrations of atmospheric particulate NO3- and NH4+ were ∼88 ± 101 nmol m-3 and ∼102 ± 102 nmol m-3, respectively, likely due to the transboundary long-range transport of pollutants. The inshore site showed a concentration ∼2 times higher than the offshore site. Considering not only dry inorganic nitrogen deposition but also wet and organic material deposition, the total atmospheric nitrogen deposition was estimated to contribute roughly 10 % to the new production in the Yellow Sea.

Acidity in rainwater and airborne suspended particles in the southwestern coast of the East Sea (Sea of Japan): Their potential impact on seawater total alkalinity.

Our understanding of the impact of atmospheric acid deposition on marine carbonate system remains limited, largely due to a lack of data regarding acidity present in atmospheric particles and precipitation. Previous research has relied on the electroneutrality-based ion balance method for indirect estimation of atmospheric acidity. In this study, atmospheric samples collected at a coastal site of South Korea were mixed with seawater to measure the change in seawater total alkalinity (ΔTAAPL) associated with atmospheric proton loading. For the precipitation samples, the measured ΔTAAPL and electroneutrality-based estimates showed a significant correlation. However, we did not observe similar results for the atmospheric particle samples. Furthermore, the decrease in oceanic TA due to ΔTAAPL was substantially smaller than that in dissolved inorganic carbon from concurrent nitrogen fertilization. Consequently, the adverse impact of acid deposition on ocean acidification or air-sea exchange of CO2 appears to be insignificant on a short-term scale.

Seasonal variation of inorganic carbon parameters and air-sea exchange of CO2 in Marian Cove, King George Island, Western Antarctic Peninsula.

Inorganic carbon parameters were observed in Marian Cove, King George Island, Western Antarctic Peninsula, to assess the impact of the Antarctic coastal regions on air-sea CO2 exchange. The variations in total alkalinity (TA) and dissolved inorganic carbon (DIC) were caused by ice melting, formation, and biological activities. The net annual air-sea CO2 flux (5.6 ± 11.8 mmol m-2 d-1) indicated that Marian Cove was a CO2 source in the atmosphere, suggesting the opposite role of the Antarctic coastal regions to the Southern Ocean in CO2 flux estimates. Finally, this study identified the controlling factors of the annual variation of TA and DIC for the first time through direct field observations in King George Island. This study indicated that Antarctic coastal regions can act as a CO2 source to the atmosphere. Thus, further investigations and continuous monitoring are required in the coastal areas to improve our understanding of global carbon cycles.

Factors affecting the subsurface aragonite undersaturation layer in the Pacific Arctic region.

This study evaluated interannual variation in the subsurface aragonite undersaturation zone (ΩAr<1 layer) in the Pacific Arctic Ocean, using data from the 2016-2019 period. The upper boundary (DEPΩ<1UB) of the ΩAr<1 layer generally formed at a depth where the contribution of corrosive Pacific water was approximately 98 %. The intensity of the Beaufort Gyre associated with freshwater accumulation mainly determined interannual variation in DEPΩ<1UB, but the direction of its effect was opposite west and east of ~166°W. The lower boundary (DEPΩ<1LB) of the ΩAr<1 layer was generally found at a depth range where equal contributions of Pacific and Atlantic water were expected. An Atlantic-origin cold saline water intrusion event in 2017 caused by an anomalous atmospheric circulation pattern significantly lifted the DEPΩ<1LB, thus the thickness of the ΩAr<1 layer decreased.

Monthly and seasonal variations in the surface carbonate system and air-sea CO2 flux of the Yellow Sea.

Surface carbonate chemistry in the Yellow Sea was investigated based on discrete seawater samples collected from 2017 to 2020 at the Socheongcho Ocean Research Station (S-ORS; 37.423°N, 124.738°E). Records of carbon parameters, including seawater CO2 partial pressure (pCO2), revealed considerable seasonal variations, with amplitudes comparable to those observed across the western part of the Yellow Sea. The study site acted as a modest sink (-0.13 mol C m-2 yr-1) for atmospheric CO2. Biological processes (primary production and respiration) and physical conditions (temperature and degree of stratification) determined seawater pCO2, which fluctuated on an intraseasonal timescale between oversaturated and undersaturated with respect to atmospheric pCO2. Variation in pCO2 was significant in summer, depending on the biological carbon drawdown and tidal mixing-induced upwelling (increased pCO2 up to ~1000 µatm). The intraseasonal variability in seawater pCO2 may bias estimated air-sea CO2 fluxes, if measurements with a coarser (seasonal) time resolution are used.

Atmospheric deposition of inorganic nutrients to the Western North Pacific Ocean.

We evaluated the potential impacts of atmospheric deposition on marine productivity and inorganic carbon chemistry in the northwestern Pacific Ocean (8-39°N, 125-157°E). The nutrient concentration in atmospheric total suspended particles decreased exponentially with increasing distance from the closest land-mass (Asia), clearly revealing anthropogenic and terrestrial contributions. The predicted mean depositional fluxes of inorganic nitrogen were approximately 34 and 15 µmol m-2 d-1 to the west and east of 140°E, respectively, which were at least two orders of magnitude greater than the inorganic phosphorus flux. On average, atmospheric particulate deposition would support 3-4% of the net primary production along the surveyed tracks, which is equivalent to ~2% of the dissolved carbon increment caused by the penetration of anthropogenic CO2. Our observations generally fell within the ranges observed over the past 18 years, despite an increasing trend of atmospheric pollution in the source regions during the same period, which implies high temporal and spatial variabilities of atmospheric nutrient concentration in the study area. Continued atmospheric anthropogenic nitrogen deposition may alter the relative abundances of nitrogen and phosphorus.