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Seasonality in size segregated biogenic, anthropogenic and sea salt sulfate aerosols over the North Atlantic

机译:北大西洋上空的生物,人为和海盐硫酸盐气溶胶按季节划分

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Size segregated aerosol sulfate concentration was measured over a south to north transect of the North Atlantic, extending from 37° N to the base of Greenland, during spring, summer and fall of 2003. Sea salt sulfate for all three seasons was found in large diameter aerosols (>0.95 μm), but spring season sea salt was also persistently found in the finest aerosols collected (<0.49 μm). Non sea salt sulfate concentrations in the 0.49-0.95 μm range (large accumulation mode) were elevated in summer (5.7 ± 7.0 nmol m~3) relative to spring (1.4 ± 0.7 nmol m~(-3)) and fall (1.3 ± 1.0 nmol m~(-3)). Non sea salt sulfate was apportioned into biogenic and anthropogenic sulfate using sulfur isotopes. Little to no biogenic sulfate was observed in the spring. However, in the summer and fall biogenic sulfate concentration averaged 2.3 ± 1.4 nmol m~(-3) and 2.0 ± 2.2 nmol m~(-3) respectively in aerosols less than 0.49 μm diameter corresponding to approximately 40% of the non sea salt sulfate load for both seasons. Anthropogenic sulfate was detectable throughout the study with the largest concentrations of fine aerosol anthropogenic sulfate (up to 76 nmol m~(-3)) observed in samples collected at lower latitudes. Stable isotopes were used to determine aerosol growth from local SO_2 oxidation in the summer. SO_2 oxidation is calculated to be significant in two aerosol growth events. These samples had the largest biogenic sulfate concentrations in the 0.49-0.95 urn range aerosols and showed high concentrations of sulfate in the 0.49-0.95 um relative to the <0.49 μm diameter aerosols. Sulfate from local SO_2 oxidation was calculated to be approximately 40% of the non sea salt sulfate present in these two events.
机译:在2003年春季,夏季和秋季,从北大西洋的南到北横断面(从北纬37°延伸到格陵兰岛的底部)测量了大小分离的气溶胶硫酸盐浓度。发现所有三个季节的海盐硫酸盐直径较大气溶胶(> 0.95μm),但在收集的最优质气溶胶(<0.49μm)中也持续发现春季海盐。夏季(5.7±7.0 nmol m〜3)相对于春季(1.4±0.7 nmol m〜(-3))升高了0.49-0.95μm范围(大积累模式)的非海盐硫酸盐浓度,而秋季(1.3± 1.0 nmol m〜(-3))。使用硫同位素将非海盐硫酸盐分配为生物和人为的硫酸盐。在春季几乎没有观察到生物硫酸盐。然而,在夏季和秋季,在直径小于0.49μm的气溶胶中,生物硫酸盐的平均浓度分别为2.3±1.4 nmol m〜(-3)和2.0±2.2 nmol m〜(-3),约占非海盐的40%两个季节的硫酸盐负荷。在整个研究过程中均可检测到人为的硫酸盐,在较低纬度收集的样品中观察到最大浓度的细小气溶胶人为的硫酸盐(高达76 nmol m〜(-3))。在夏季,稳定同位素用于确定局部SO_2氧化引起的气溶胶生长。计算出在两个气溶胶生长事件中,SO_2的氧化非常重要。这些样品在0.49-0.95微米范围的气溶胶中具有最大的生物硫酸盐浓度,相对于直径小于0.49μm的气溶胶,在0.49-0.95 um中显示高浓度的硫酸盐。计算得出,来自局部SO_2氧化的硫酸盐约为这两种情况下存在的非海盐硫酸盐的40%。

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