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Aerosol composition and sources in the central Arctic Ocean during ASCOS

机译:ASCOS期间北冰洋中部的气溶胶成分和来源

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Measurements of submicron aerosol chemical composition were made over the central Arctic Ocean from 5 August to 8 September 2008 as a part of the Arctic Summer Cloud Ocean Study (ASCOS) using an aerosol mass spectrometer (AMS). The median levels of sulphate and organics for the entire study were 0.051 and 0.055 μ g m(~(-3), respectively. Positive matrix factorisation was performed on the entire mass spectral time series and this enabled marine biogenic and continental sources of particles to be separated. These factors accounted for 33% and 36% of the sampled ambient aerosol mass, respectively, and they were both predominantly composed of sulphate, with 47% of the sulphate apportioned to marine biogenic sources and 48% to continental sources, by mass. Within the marine biogenic factor, the ratio of methane sulphonate to sulphate was 0.25 ± 0.02, consistent with values reported in the literature. The organic component of the continental factor was more oxidised than that of the marine biogenic factor, suggesting that it had a longer photochemical lifetime than the organics in the marine biogenic factor. The remaining ambient aerosol mass was apportioned to an organic-rich factor that could have arisen from a combination of marine and continental sources. In particular, given that the factor does not correlate with common tracers of continental influence, we cannot rule out that the organic factor arises from a primary marine source.
机译:作为北极夏季云海洋研究(ASCOS)的一部分,使用气溶胶质谱仪(AMS)在2008年8月5日至9月8日在北冰洋中部进行了亚微米气溶胶化学成分的测量。整个研究中硫酸盐和有机物的中位水平分别为0.051和0.055μgm(〜(-3)。在整个质谱时间序列上进行正矩阵分解,这使得海洋生物源和大陆的颗粒来源成为可能。这些因素分别占采样的环境气溶胶质量的33%和36%,并且它们都主要由硫酸盐组成,按质量计,硫酸盐的47%分配给海洋生物源,大陆的48%。在海洋生物成因中,甲烷磺酸盐与硫酸盐之比为0.25±0.02,与文献报道的值一致,大陆性因素的有机成分比海洋生物成因中的有机成分被氧化得更多,这表明它具有更长的时间。光化学寿命比海洋生物成因中的有机物要长,剩余的周围气溶胶质量被分配给富含有机物的因素,这可能是由于交流引起的。海洋和大陆资源的结合。特别是,鉴于该因素与大陆性影响的常见示踪剂不相关,我们不能排除有机因素来自主要海洋资源的情况。

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