Description: Transparent exopolymer particles (TEP) and Coomassie stainable particles (CSP) are gel-like particles, ubiquitous in the ocean, that affect important biogeochemical processes including organic carbon cycling by planktonic food webs. Despite much research on both groups of particles (especially TEP) over many years, whether they exist as distinctly stainable fractions of the same particles or as independent particles, each with different driving factors, remains unclear. To address this question, we examined the temporal dynamics of TEP and CSP over 2 complete seasonal cycles at 2 coastal sites in the Northwestern Mediterranean Sea, the Blanes Bay Microbial Observatory (BBMO) and the L’Estartit Oceanographic Station (EOS), as well as their spatial distribution along a coast-to-offshore transect. Biological, chemical, and physical variables were measured in parallel. Surface concentrations (mean ± standard deviation [SD]) of TEP were 36.7 ± 21.5 µg Xanthan Gum (XG) eq L–1 at BBMO and 36.6 ± 28.3 µg XG eq L–1 at EOS; for CSP, they were 11.9 ± 6.1 µg BSA eq L–1 at BBMO and 13.0 ± 5.9 µg BSA eq L–1 at EOS. Seasonal variability was more evident at EOS, where surface TEP and CSP concentrations peaked in summer and spring, respectively, and less predictable at the shore-most station, BBMO. Vertical distributions between surface and 80 m, monitored at EOS, showed highest TEP concentrations within the surface mixed layer during the stratification period, whereas CSP concentrations were highest before the onset of summer stratification. Phytoplankton were the main drivers of TEP and CSP distributions, although nutrient limitation and saturating irradiance also appeared to play important roles. The dynamics and distribution of TEP and CSP were uncoupled both in the coastal sites and along the transect, suggesting that they are different types of particles produced and consumed differently in response to environmental variability.

Description: Ocean biogeochemistry involves the production and consumption of an array of organic compounds and halogenated trace gases that influence the composition and reactivity of the atmosphere, air quality, and the climate system. Some of these molecules affect tropospheric ozone and secondary aerosol formation and impact the atmospheric oxidation capacity on both regional and global scales. Other emissions undergo transport to the stratosphere, where they contribute to the halogen burden and influence ozone. The oceans also comprise a major sink for highly soluble or reactive atmospheric gases. These issues are an active area of research by the SOLAS (Surface Ocean Lower Atmosphere) community. This article provides a status report on progress over the past decade, unresolved issues, and future research directions to understand the influence of ocean biogeochemistry on gas-phase atmospheric chemistry. Common challenges across the subject area involve establishing the role that biology plays in controlling the emissions of gases to the atmosphere and the inclusion of such complex processes, for example involving the sea surface microlayer, in large-scale global models.