Abstract Oceanic production and occurrence of dimethyl sulfide (DMS) and its subsequent ventilation to the atmosphere significantly contribute to the global sulfur cycle and impact the climate regulation. Spatial distributions of DMS, dimethylsulfoniopropionate (DMSP, precursor of DMS), and dimethyl sulfoxide (DMSO, oxidation product of DMS), production and removal processes of DMS (including biological production, microbial consumption, photo‐degradation, and sea‐to‐air exchange), and biogenic contributions to the atmospheric sulfate burden were simultaneously studied in the western Pacific Ocean during winter. Sea surface DMS, DMSP, and DMSO were strongly correlated and had similar distribution patterns. The DMS photo‐degradation efficiency ratio (normalized using incident photon flux density) for ultraviolet B radiation (UVB): ultraviolet A radiation (UVA): photosynthetically active radiation (PAR) was 391: 36: 1. However, considering the solar spectral composition, the actual contributions of UVB, UVA, and PAR to DMS photo‐degradation in surface waters were 40.6% ± 10.7%, 41.2% ± 15.6%, and 18.2% ± 7.2%, respectively. When integrated across the entire mixed layer, UVA and PAR became the dominant drivers, accounting for 45.2% ± 18.0% and 38.0% ± 17.3% of DMS photo‐degradation, respectively, as UVB was significantly attenuated in seawater. The DMS budget of the entire mixed layer indicated that microbial consumption, photo‐degradation, and ventilation accounted for about 74.3% ± 11.9%, 19.3% ± 9.3%, and 6.5% ± 4.0% of total DMS removal, respectively. Even if ventilation was a minor DMS removal pathway, DMS emissions still contributed approximately 45.2% ± 25.6% of the atmospheric non‐sea‐salt sulfate burden over the western Pacific Ocean.
Alkalinity was determined by Gran titration with an autotitrator (Metrohm 794 basic Titrino) using 0.1 M HCl at 20 degrees C. Report includes alkalinity, correction factor (if applicable), and pH.
Abstract Methanol metabolism can play an important role in marine carbon cycling. We made contemporaneous measurements of methanol concentration and consumption rates in the northwest Pacific Ocean to constrain the pathways and dynamics of methanol cycling. Methanol was detected in relatively low concentrations (<12–391 nM), likely due to rapid biological turnover. Rates of methanol oxidation to CO 2 (0.9–130.5 nmol L −1 day −1 ) were much higher than those of assimilation into biomass (0.09–6.8 nmol L −1 day −1 ), suggesting that >89.7% of methanol was utilized as an energy source. Surface water acted as a net methanol sink at most sites, with an average flux of 9 μmol L −1 day −1 . Atmospheric deposition accounted for 22.7% of microbial methanol consumption in the mixed layer, illustrating that the atmosphere is less important than internal processes for driving methanol cycling in these pelagic waters.
Abstract Aerobic methane oxidation (MOx) mediated by methanotrophs is a crucial mechanism in controlling methane emissions from the surface ocean to the atmosphere. Coastal waters dominate global oceanic methane emissions, but the dynamics, controls and roles of MOx remain largely unconstrained in the marginal seas around China. Here, we conducted a variety of biogeochemical analyses to investigate the controls of methane cycling and the dynamics of methanotrophic activity in the East China Sea and Yellow Sea. Methane was supersaturated in the surface seawater and the concentrations ranged from 2.8 to 19.8 nM. The distribution of methane was regulated by the sources and sinks, which were influenced largely by hydrological and biogeochemical factors. Methane was turned over rapidly with high rates ( k : 5 × 10 −4 –0.04 d −1 ), indicating the enzymatic capability of methanotrophic biomass to metabolize methane. Rates of MOx varied significantly between sites (1 × 10 −3 –0.60 nM d −1 ) and relatively high MOx rates were observed in shallow waters. MOx exhibited the Michaelis‐Menten kinetics with the V max of 0.30 nM d −1 and a K m of 78.3 nM. Methanotrophic activity was impacted by environmental factors such as methane availability, nutrient levels, bacterial production and temperature. Nutrient addition experiments demonstrated that phosphate elevated MOx rates, while the activity was largely inhibited by ammonium probably due to competitive inhibition of the methane monooxygenase by ammonia. Comparing the depth‐integrated MOx rates with the air‐sea fluxes at selected sites showed that methane consumed through microbial oxidation accounted for up to 78.1% of the total methane loss (=sum of MOx rates and air‐sea flux), highlighting the role of MOx as a microbial filter for methane emissions.
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