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Multiphase modeling of nitrate photochemistry in the quasi-liquid layer (QLL): implications for NOx release from the Arctic and coastal Antarctic snowpack

Abstract

We utilize a multiphase model, CON-AIR (<B>Con</B>densed Phase to <B>Air</B> Transfer Model), to show that the photochemistry of nitrate (NO<sub>3</sub><sup>&minus;</sup>) in and on ice and snow surfaces, specifically the quasi-liquid layer (QLL), can account for NO<sub>x</sub> volume fluxes, concentrations, and [NO]/[NO<sub>2</sub>] (γ=[NO]/[NO<sub>2</sub>]) measured just above the Arctic and coastal Antarctic snowpack. Maximum gas phase NO<sub>x</sub> volume fluxes, concentrations and γ simulated for spring and summer range from 5.0&times;10<sup>4</sup> to 6.4&times;10<sup>5</sup> molecules cm<sup>&minus;3</sup> s<sup>&minus;1</sup>, 5.7&times;10<sup>8</sup> to 4.8&times;10<sup>9</sup> molecules cm<sup>&minus;3</sup>, and ~0.8 to 2.2, respectively, which are comparable to gas phase NO<sub>x</sub> volume fluxes, concentrations and γ measured in the field. The model incorporates the appropriate actinic solar spectrum, thereby properly weighting the different rates of photolysis of NO<sub>3</sub><sup>&minus;</sup> and NO<sub>2</sub><sup>&minus;</sup>. This is important since the immediate precursor for NO, for example, NO<sub>2</sub><sup>&minus;</sup>, absorbs at wavelengths longer than nitrate itself. Finally, one-dimensional model simulations indicate that both gas phase boundary layer NO and NO<sub>2</sub> exhibit a negative concentration gradient as a function of height although [NO]/[NO<sub>2</sub>] are approximately constant. This gradient is primarily attributed to gas phase reactions of NO<sub>x</sub> with halogens oxides (i.e. as BrO and IO), HO<sub>x</sub>, and hydrocarbons, such as CH<sub>3</sub>O<sub>2</sub>

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