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Eddy flux measurements of sulfur dioxide deposition to the sea surface

机译:二氧化硫沉积到海面的涡流磁通测量

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Deposition to the sea surface is a major atmospheric loss pathway for many important trace gases, such as sulfur dioxide (SO2). The air-sea transfer of SO2 is controlled entirely on the atmospheric side of the air-sea interface due to high effective solubility and other physicalchemical properties. There have been few direct field measurements of such fluxes due to the challenges associated with making fast-response measurements of highly soluble trace gases at very low ambient levels. In this study, we report direct eddy covariance air-sea flux measurements of SO2, sensible heat, water vapor, and momentum. The measurements were made over shallow coastal waters from the Scripps Pier, La Jolla, CA, using negative ion chemical ionization mass spectrometry as the SO2 sensor. The observed transfer velocities for SO2, sensible heat, water vapor, and momentum and their wind speed dependences indicate that SO2 fluxes can be reliably measured using this approach. As expected, the transfer velocities for SO2, sensible heat, and water vapor are lower than that for momentum, demonstrating the contribution of molecular diffusion to the overall air-side resistance to gas transfer. Furthermore, transfer velocities of SO2 were lower than those of sensible heat and water vapor when observed simultaneously. This result is attributed to diffusive resistance in the interfacial layer of the air-sea interface.
机译:对海面的沉积是主要的大气损耗途径,用于许多重要的痕量气体,例如二氧化硫(SO 2)。由于高有效的溶解度和其他物理化学性质,SO2的空气海移在空中界面的大气侧控制。由于与在非常低的环境水平下的高度可溶性痕量气体的快速响应测量结果相关的挑战,这种助焊剂存在很少的直接现场测量。在这项研究中,我们报告了SO2,明智的热量,水蒸气和动量的直接涡旋协方差空中通量测量。使用负离离子化学电离质谱法作为SO2传感器,在Scripps Pier,La Jolla,CA的浅沿海水中进行测量。所观察到的SO2,明智的热,水蒸气和动量及其风速依赖性的转移速度表明SO2助熔剂可以使用这种方法可靠地测量。如所预期的,SO2,明智的热量和水蒸气的转移速度低于动量的转移速度,证明了分子扩散到总空气转移的整体空气侧抗性的贡献。此外,在同时观察时,SO2的转移速度低于显微镜热量和水蒸气的转移速度。该结果归因于空中海界面的界面层中的扩散抗性。

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