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Air–sea fluxes of oxygenated volatile organic compounds across the Atlantic Ocean

机译:跨大西洋氧化挥发性有机化合物的空中海洋助熔剂

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We present air–sea fluxes of oxygenated volatile organics compounds (OVOCs) quantified by eddy covariance (EC) during the Atlantic Meridional Transect cruise in 2012. Measurements of acetone, acetaldehyde, and methanol in air as well as in water were made in several different oceanic provinces and over a wide range of wind speeds (1–18 m s?1). The ocean appears to be a net sink for acetone in the higher latitudes of the North Atlantic but a source in the subtropics. In the South Atlantic, seawater acetone was near saturation relative to the atmosphere, resulting in essentially zero net flux. For acetaldehyde, the two-layer model predicts a small oceanic emission, which was not well resolved by the EC method. Chemical enhancement of air–sea acetaldehyde exchange due to aqueous hydration appears to be minor. The deposition velocity of methanol correlates linearly with the transfer velocity of sensible heat, confirming predominant airside control. We examine the relationships between the OVOC concentrations in air as well as in water, and quantify the gross emission and deposition fluxes of these gases.
机译:我们在2012年的大西洋经过横切巡航期间呈现通过涡旋协方差(EC)量化的空中挥发性有机物(OVOC)。在几种不同的情况下制造丙酮,乙醛,空气中的丙酮,乙醛和甲醇的测量海洋省份和广泛的风速(1-18毫秒?1)。海洋似乎是丙酮的净水槽,在北大西洋的高层纬度,但副数据集中的源泉。在南部大西洋,海水丙酮相对于大气饱和,导致基本上净净磁通量。对于乙醛,两层模型预测了小的海洋发射,其通过EC方法并不充分解决。由于水性水化而导致的空中海乙醛交换的化学增强似乎是较小的。甲醇的沉积速度随着明智的热量的传递速度与显微速度线性相关,确认主要的空间控制。我们检查空气中的OVOC浓度与水中的关系,并量化这些气体的总排放和沉积助熔剂。

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