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Long-term studies of suspended particulate matter (SPM) and organic compounds (OCs)—Corg, lipids, hydrocarbons (aliphatic—AHCs and polycyclic aromatic—PAHs), and chlorophyll a in the snow cover of the Arctic (Franz Victoria Trough, Mendeleev Rise, White Sea) and Antarctica (in the coastal waters on fast ice and on the mainland near Russian stations) were generalized. It was shown that in the Arctic, the influence of continental air masses leads to an increase in OCs in snow. Therefore, despite the fact that the Franz Victoria Trough and the Mendeleev Rise are at the same latitude (82° N), the OCs content in the snow in the region of the Mendeleev Rise was lower for aliphatic hydrocarbons 5 and 14–18 μg/L. In the White Sea, the AHC content in the snow and the upper layers of the ice in the mouth of the Severnaya Dvina River and in the Kandalaksha Bay was higher than that in the lower layers of the ice and sharply decreased with distance from the emission sources. As a result, the snow was supplied mainly by pyrogenic PAHs. In the Antarctica, the lowest OCs levels in atmosphere were found in areas where coastal hills are covered with snow. The maximum SPM and AHCs concentration was found in the sludge (SPM—to 4.37 mg/L, AHC—to 33 μg/L). An increase in the concentration of OCs and SPM in snow sampled on the continent took place in the areas of stations and oases (St. Novolazarevskaya) where the predominance of mineral particles in the SPM was registered. In the area of the operating stations, mainly low molecular weight PAHs with the dominance of petroleum PAHs were found in the SPM of snow and in mosses. [ABSTRACT FROM AUTHOR]

We apply principles of Gibbs phase plane chemistry across the entire ocean-atmosphere interface to investigate aerosol generation and geophysical transfer issues. Marine surface tension differences comprise a tangential pressure field controlling trace gas fluxes, primary organic inputs, and sea spray salt injections, in addition to heat and momentum fluxes. Mapping follows from the organic microlayer composition, now represented in ocean system models. Organic functional variations drive the microforcing, leading to (1) reduced turbulence and (by extension) laminar gas-energy diffusion; plus (2) altered bubble film mass emission into the boundary layer. Interfacial chemical behaviors are, therefore, closely reviewed as the background. We focus on phase transitions among two dimensional “solid, liquid, and gaseous” states serving as elasticity indicators. From the pool of dissolved organic carbon (DOC) only proteins and lipids appear to occupy significant atmospheric interfacial areas. The literature suggests albumin and stearic acid as the best proxies, and we distribute them through ecodynamic simulation. Consensus bulk distributions are obtained to control their adsorptive equilibria. We devise parameterizations for both the planar free energy and equation of state, relating excess coverage to the surface pressure and its modulus. Constant settings for the molecular surrogates are drawn from laboratory study and successfully reproduce surfactant solid-to-gas occurrence in compression experiments. Since DOC functionality measurements are rare, we group them into super-ecological province tables to verify aqueous concentration estimates. Outputs are then fed into a coverage, tension, elasticity code. The resulting two dimensional pressure contours cross a critical range for the regulation of precursor piston velocity, bubble breakage, and primary aerosol sources plus ripple damping. Concepts extend the water-air adsorption theory currently embodied in our OCEANFILMS aerosol emissions package, and the two approaches could be inserted into Earth System Models together. Uncertainties in the logic include kinetic and thermochemical factors operating at multiple scales. [ABSTRACT FROM AUTHOR]