Quantification of CH4 loss and transport in dissolved plumes of the Santa Barbara Channel, California

Abstract

Methane (CH4) emitted into the coastal ocean faces two primary fates: escape to the atmosphere or prolonged dissolution that allows sufficient time for oxidation by methanotrophic bacteria. The partitioning of CH4 between these fates is modulated by physical, chemical and biological factors, including the distribution of CH4 in the water, temperature, wind speed, water movement, and the biological CH4 oxidation rate. Because of the underlying complexity, studies rarely quantify all of these factors in unison, thereby leaving gaps in our understanding of CH4 biogeochemistry in the coastal ocean. In this study we estimated the partitioning of CH4 between transport, microbial oxidative loss, and sea–air transfer in a defined plume of dissolved CH4 originating from one of the world's largest seep fields, near Coal Oil Point (COP) in the Santa Barbara Channel, California. Depth distributions of CH4 concentration, biologically mediated oxidation rate, and current velocity were quantified at 12 stations in a 198km2 area down-current from COP on July 4–5, 2007. Six stations were sampled again on July 7, 2007 to evaluate temporal plume variability. The observed CH4 distribution revealed two distinct CH4 plumes: a shallow plume centered at ∼40m and a deeper plume centered at ∼200m. The shallow plume originates at COP; the source of the deeper CH4 plume is not known. Cross-sections of both plumes were used to calculate transport and loss terms for dissolved CH4. The results indicate that the majority of the dissolved CH4 is advected and diffuses horizontally by turbulence whereas microbial oxidation, sea–air gas transfer, and vertical turbulent diffusion are less significant. Based on rates estimated in the study area, a model was developed to simulate the fate of the dissolved CH4. The model results suggest that 60% of the CH4 of the sampled plumes will ultimately be microbially oxidized and 40% will be transferred to the atmosphere by sea–air gas exchange under the sampling conditions. These results illustrate the significance of microbial CH4 oxidation in coastal oceans.