首页> 外文期刊>Journal of the Atmospheric Sciences >Aerosol properties and chemical apportionment of aerosol optical depth at locations off the US east coast in July and August 2001
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Aerosol properties and chemical apportionment of aerosol optical depth at locations off the US east coast in July and August 2001

机译:2001年7月和2001年8月在美国东海岸以外地区的气溶胶性质和气溶胶光学深度的化学分配

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Airborne in situ measurements of vertical profiles of the aerosol light scattering coefficient, light absorption coefficient, and single scattering albedo (omega(0) ) are presented for locations off the East Coast of the United States in July-August 2001. The profiles were obtained in relatively clean air, dominated by airflows that had passed over Canada and the Atlantic Ocean. Comparisons of aerosol optical depths (AODs) at 550 nm derived from airborne in situ and sun-photometer measurements agree, on average, to within 0.034 +/- 0.021. A frequency distribution of omega(0) measured in the atmospheric boundary layer off the coast yields an average value of omega(0) = 0.96 +/- 0.03 at 550 am. Values for the mass scattering efficiencies of sulfate and total carbon (organic and black carbon) derived from a multiple linear regression are 6.0 +/- 1.0 m(2) (g SO4=)(-1) and 2.6 +/- 0.9 m(2) (g C)(-1), respectively. Measurements of sulfate and total carbon mass concentrations are used to estimate the contributions of these two major components of the submicron aerosol to the AOD. Mean percentage contributions to the AOD from sulfate, total carbon, condensed water, and absorbing aerosols are 38% +/- 8%, 26% +/- 9%, 32% +/- 9%, and 4% +/- 2%, respectively. The sensitivity of the above results to the assumed values of the hygroscopic growth factors for the particles are examined and it is found that, although the AOD derived from the in situ measurements can vary by as much as 20%, the average value of omega(0) is not changed significantly. The results are compared with those obtained in the same region in 1996 under more polluted conditions.
机译:2001年7月至2001年8月在美国东海岸以外的位置,进行了气溶胶光散射系数,光吸收系数和单散射反照率(omega(0))垂直剖面的机载原位测量。获得了这些剖面在相对清洁的空气中,主要由流经加拿大和大西洋的气流所控制。从机载原位和太阳光度计测量得出的550 nm气溶胶光学深度(AOD)的比较平均在0.034 +/- 0.021范围内。在沿海大气边界层中测得的omega(0)频率分布在550 am产生omega(0)= 0.96 +/- 0.03的平均值。多元线性回归得出的硫酸盐和总碳(有机碳和黑碳)的质量散射效率值为6.0 +/- 1.0 m(2)(g SO4 =)(-1)和2.6 +/- 0.9 m( 2)(g C)(-1)。硫酸盐和总碳质量浓度的测量值用于估算亚微米气溶胶的这两个主要成分对AOD的贡献。硫酸盐,总碳,冷凝水和吸收性气溶胶对AOD的平均贡献百分比为38%+/- 8%,26%+/- 9%,32%+/- 9%和4%+/- 2 %, 分别。检查了以上结果对颗粒的吸湿性生长因子的假定值的敏感性,发现尽管原位测量得出的AOD可能相差20%,但Ω( 0)没有明显变化。将结果与1996年同一地区在更污染的条件下获得的结果进行比较。

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