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A physically based framework for modeling the organic fractionation of sea spray aerosol from bubble film Langmuir equilibria

机译:一个基于物理的框架,用于模拟气泡膜Langmuir平衡的海雾气溶胶的有机分离

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摘要

The presence of a large fraction of organic matter in primary sea spray aerosol (SSA) can strongly affect its cloud condensation nuclei activity and interactions with marine clouds. Global climate models require new parameterizations of the SSA composition in order to improve the representation of these processes. Existing proposals for such a parameterization use remotely sensed chlorophyll concentrations as a proxy for the biogenic contribution to the aerosol. However, both observations and theoretical considerations suggest that existing relationships with chlorophyll , derived from observations at only a few locations, may not be representative for all ocean regions. We introduce a novel framework for parameterizing the fractionation of marine organic matter into SSA based on a competitive Langmuir adsorption equilibrium at bubble surfaces. Marine organic matter is partitioned into classes with differing molecular weights, surface excesses, and Langmuir adsorption parameters. The classes include a lipid-like mixture associated with labile dissolved organic carbon (DOC), a polysaccharide-like mixture associated primarily with semilabile DOC, a protein-like mixture with concentrations intermediate between lipids and polysaccharides, a processed mixture associated with recalcitrant surface DOC, and a deep abyssal humic-like mixture. Box model calculations have been performed for several cases of organic adsorption to illustrate the underlying concepts. We then apply the framework to output from a global marine biogeochemistry model, by partitioning total dissolved organic carbon into several classes of macromolecules. Each class is represented by model compounds with physical and chemical properties based on existing laboratory data. This allows us to globally map the predicted organic mass fraction of the nascent submicron sea spray aerosol. Predicted relationships between chlorophyll and organic fraction are similar to existing empirical parameterizations, but can vary between biologically productive and nonproductive regions, and seasonally within a given region. Major uncertainties include the bubble film thickness at bursting, and the variability of organic surfactant activity in the ocean, which is poorly constrained. In addition, polysaccharides may enter the aerosol more efficiently than Langmuir adsorption would suggest. Potential mechanisms for enrichment of polysaccharides in sea spray include the formation of marine colloidal particles that may be more efficiently swept up by rising bubbles, and cooperative adsorption of polysaccharides with proteins or lipids. These processes may make important contributions to the aerosol, but are not included here. This organic fractionation framework is an initial step towards a closer linking of ocean biogeochemistry and aerosol chemical composition in Earth system models. Future work should focus on improving constraints on model parameters through new laboratory experiments or through empirical fitting to observed relationships in the real ocean and atmosphere, as well as on atmospheric implications of the variable composition of organic matter in sea spray.
机译:初级海洋喷雾气溶胶(SSA)中存在很大一部分有机物质,可以强烈影响其云凝结核的活动以及与海洋云的相互作用。全球气候模型要求对SSA组成进行新的参数化,以改善这些过程的代表性。用于这种参数化的现有建议使用遥感的叶绿素浓度作为对气溶胶的生物成因的替代。然而,观测和理论考虑都表明,仅在少数几个地点观测到的与叶绿素的现有关系可能无法代表所有海洋区域。我们介绍了一个新颖的框架,用于基于气泡表面的竞争性Langmuir吸附平衡,将海洋有机物的分离参数化为SSA。海洋有机物被分为具有不同分子量,表面过量度和Langmuir吸附参数的类别。这些类别包括与不稳定的可溶性有机碳(DOC)相关的类脂质混合物,与半不稳定的DOC主要相关的多糖类混合物,在脂质和多糖之间的浓度介于中间的蛋白质样混合物,与顽固的表面DOC相关的加工混合物,以及深渊的腐殖质样混合物。已对几种有机吸附情况进行了盒模型计算,以说明基本概念。然后,我们通过将总溶解有机碳划分为几类大分子,将该框架应用于全球海洋生物地球化学模型的输出。每个类别均由基于现有实验室数据的具有物理和化学性质的模型化合物表示。这使我们能够全局绘制新生的亚微米海喷雾气溶胶的预测有机质量分数。叶绿素和有机物组分之间的预测关系类似于现有的经验参数化,但是在生物生产性和非生产性区域之间以及给定区域内的季节之间可能会有所不同。主要的不确定因素包括破裂时气泡膜的厚度以及海洋中有机表面活性剂活性的变化性,该变化性受到的约束较弱。此外,多糖可能比Langmuir吸附法更有效地进入气雾剂。在海浪中富集多糖的潜在机制包括形成海洋胶体颗粒(可能会被上升的气泡更有效地清除),以及多糖与蛋白质或脂质的协同吸附。这些过程可能对气溶胶做出重要贡献,但此处未包括在内。这种有机分级分离框架是朝着地球系统模型中海洋生物地球化学与气溶胶化学成分之间更紧密联系迈出的第一步。未来的工作应侧重于通过新的实验室实验或通过对实际海洋和大气中观测到的关系进行经验拟合来改善对模型参数的约束,以及海浪中有机物的可变成分对大气的影响。

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