ALBERT

Description: Despite the huge extent of the ocean's surface, until now relatively little attention has been paid to the sea surface microlayer (SML) as the ultimate interface where heat, momentum and mass exchange between the ocean and the atmosphere takes place. Via the SML, large-scale environmental changes in the ocean such as warming, acidification, deoxygenation, and eutrophication potentially influence cloud formation, precipitation, and the global radiation balance. Due to the deep connectivity between biological, chemical, and physical processes, studies of the SML may reveal multiple sensitivities to global and regional changes. Understanding the processes at the ocean's surface, in particular involving the SML as an important and determinant interface, could therefore provide an essential contribution to the reduction of uncertainties regarding ocean-climate feedbacks. This review identifies gaps in our current knowledge of the SML and highlights a need to develop a holistic and mechanistic understanding of the diverse biological, chemical, and physical processes occurring at the ocean-atmosphere interface. We advocate the development of strong interdisciplinary expertise and collaboration in order to bridge between ocean and atmospheric sciences. Although this will pose significant methodological challenges, such an initiative would represent a new role model for interdisciplinary research in Earth System sciences.

Description: This paper proposes improved guidelines for dissolved organic matter (DOM) isolation by solid phase extraction (SPE) with a styrene-divinylbenzene copolymer (PPL) sorbent, which has become an established method for the isolation of DOM from natural waters, because of its ease of application and appreciable carbon recovery. Suwannee River water was selected to systematically study the effects of critical SPE variables such as loading mass, concentration, flow rate, and up-scaling on the extraction selectivity of the PPL sorbent. High-field Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS) and proton nuclear magnetic resonance (H-1 NMR) spectroscopy were performed to interpret the DOM chemical space of eluates, as well as permeates and-wash liquids with molecular resolution. Up to 89% dissolved organic carbon (DOC) recovery was obtained with a DOC/PPL mass ratio of 1:800 at a DOC concentration of 20 mg/L. With the 0 application of larger loading volumes, low proportions of highly oxygenated compounds were retained on the PPL sorbent. The effects of the flow rate on the extraction selectivity of the sorbent were marginal. Up-scaling had a limited effect on the extraction selectivity with the exception of increased self-esterification with a methanol solvent, resulting in methyl ester groups. Furthermore, the SPE/PPL extract exhibited highly authentic characteristics in comparison with original water and reverse osmosis samples. These findings will be useful for reproducibly isolating DOM with representative molecular compositions from various sources and concentrations and minimizing potential inconsistencies among interlaboratory comparative studies.

Description: Dissolved organic carbon (DOC) plays critical roles in marine carbon cycling, but its sources and sinks remain uncertain. In this study, we monitored DOC exudation rates of Sargassum natans under visible light (lambda 〉 390 nm) and solar radiation. DOC release rates ranged from 7 to 10 mu g C g(biomass)(-1) hr(-1) (wet weight) under visible light, but increased to 23 to 41 mu g C g(biomass)(-1) hr(-1) when exposed to natural sunlight. Results indicate that DOC released by Sargassum could amount to 0.3 to 1.2 Tg C/year, potentially contributing significantly to the marine DOC pool in the Gulf of Mexico and Western North Atlantic. We employed the Folin-Ciocalteu phenolic content method, nuclear magnetic resonance (NMR) spectroscopy, and ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) to characterize the diverse pool of organic compounds exuded from Sargassum. Results from these complementary methods showed that Sargassum release large quantities of phlorotannins, a class of polyphenols that have very similar properties to terrestrial DOC. These phlorotannins and their oxygenated phenolic derivatives exhibit a high hydrogen deficiency and functionalization (i.e., 4 to 6 oxygen atoms per aromatic ring), representing 5 to 18% of the released DOC isolated by solid phase extraction. Thus, Sargassum is the largest biological source of open ocean polyphenols recorded to date. The amount of polyphenolic DOC released by Sargassum challenges previous beliefs that all polyphenols found within the oceans are remnants of terrestrial organic matter, although the stability of phlorotannins and their derivatives needs to be further evaluated.