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Improving constraints on the sources and distribution of sea salt aerosols in polar regions.

机译:改善对极地地区海盐气溶胶的来源和分布的限制。

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摘要

Sea salt aerosols (SSA) have a critical influence on radiation, cloud formation and chemistry of the polar atmosphere. In addition to the commonly accepted open ocean source of SSA, several studies have suggested that SSA can be produced by sublimation of windblown salty snow or frost flowers over sea ice-covered regions. To estimate and compare the role of sea ice and open ocean sources, we implement a blowing snow emission scheme and a frost flower emission scheme for the sea ice-covered regions in the GEOS-Chem global 3D chemical transport model. We analyze multi-year observations of SSA mass concentrations at three Arctic sites (Barrow, Alaska; Alert, Canada; Zeppelin, Svalbard) and two Antarctic sites (Neumayer and Dumont d'Urville) and compare them to simulations with the GEOS-Chem model for 2001-2008. Simulations including only open-ocean SSA emission fail to reproduce the observed winter maximum in SSA mass concentrations at these sites. In winter, the model underestimate ranges from factors of 3 to 25. Including a blowing snow or frost flower source of SSA leads to improved agreement with the observed seasonality. The blowing snow simulation captures the daily variability of observed SSA mass concentrations, while the frost flower simulation fails to do so. Based on the comparison to surface observations, for the regions poleward of 60° latitude, we estimate that the total annual SSA emission (submicron and supermicron) from the open ocean is 31 Tg/yr over the Arctic and 56 Tg/yr over the Antarctic, which are an order of magnitude larger than those from blowing snow or frost flowers. We find that in the submicron range, however, SSA emissions from blowing snow (1 Tg/yr over the Arctic and 2.3 Tg/yr over the Antarctic for those on all sea ice; and 0.6 Tg/yr over the Arctic and 1.9 Tg/yr over the Antarctic for those on first-year sea ice) or frost flowers (0.3 Tg/yr over the Arctic and 0.2 Tg/yr over the Antarctic) are comparable to, or even larger than, those from open ocean.
机译:海盐气溶胶(SSA)对辐射,云的形成和极地大气的化学性质具有至关重要的影响。除了普遍认可的SSA开放海资源外,多项研究表明,可以通过在被冰覆盖的海域升起风吹咸雪或霜花来生产SSA。为了估算和比较海冰和开放海源的作用,我们在GEOS-Chem全球3D化学运输模型中为覆盖海冰的地区实施了吹雪排放方案和霜花排放方案。我们分析了在三个北极站点(阿拉斯加的巴罗;加拿大的Alert,加拿大的Zeppelin,斯瓦尔巴特群岛)和两个南极站点(Neumayer和Dumont d'Urville)对SSA质量浓度的多年观测结果,并将其与GEOS-Chem模型的模拟结果进行了比较适用于2001-2008年。仅包括开放海洋SSA排放的模拟无法重现这些站点观测到的SSA质量浓度的冬季最大值。在冬季,该模型低估了3到25的范围。包括SSA的吹雪或霜冻花源可以改善与观测季节的一致性。吹雪模拟捕获了观测到的SSA质量浓度的每日变化,而霜花模拟则没有。根据与地面观测结果的比较,对于纬度为60°的极地地区,我们估计北极地区公海每年的SSA排放总量(亚微米和超微米)为31 Tg / yr,南极为56 Tg / yr。 ,比吹雪或霜花的数量大一个数量级。但是,我们发现,在亚微米范围内,吹雪产生的SSA排放量(北极上所有海冰上的排放量分别为1 Tg / yr和南极上空的2.3 Tg / yr;北极上空为0.6 Tg / yr和1.9 Tg / yr)对于第一年的海冰来说,南极的年降水量)或霜花(北极上的0.3 Tg /年,南极上的0.2 Tg /年)可以与甚至比公海的大。

著录项

  • 作者

    Huang, Jiayue.;

  • 作者单位

    University of Washington.;

  • 授予单位 University of Washington.;
  • 学科 Atmospheric sciences.;Atmospheric chemistry.
  • 学位 Masters
  • 年度 2016
  • 页码 61 p.
  • 总页数 61
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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