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沿抵达百慕大的北美空气轨迹的降水的气溶胶响应。

Aerosol responses to precipitation along North American air trajectories arriving at Bermuda.

作者信息

Dadashazar Hossein, Alipanah Majid, Hilario Miguel Ricardo A, Crosbie Ewan, Kirschler Simon, Liu Hongyu, Moore Richard H, Peters Andrew J, Scarino Amy Jo, Shook Michael, Thornhill K Lee, Voigt Christiane, Wang Hailong, Winstead Edward, Zhang Bo, Ziemba Luke, Sorooshian Armin

机构信息

Department of Chemical and Environmental Engineering, University of Arizona, Tucson, AZ, USA.

Department of Systems and Industrial Engineering, University of Arizona, Tucson, AZ, USA.

出版信息

Atmos Chem Phys. 2021 Nov 2;21(21):16121-16141. doi: 10.5194/acp-21-16121-2021.

Abstract

North American pollution outflow is ubiquitous over the western North Atlantic Ocean, especially in winter, making this location a suitable natural laboratory for investigating the impact of precipitation on aerosol particles along air mass trajectories. We take advantage of observational data collected at Bermuda to seasonally assess the sensitivity of aerosol mass concentrations and volume size distributions to accumulated precipitation along trajectories (APT). The mass concentration of particulate matter with aerodynamic diameter less than 2.5 μm normalized by the enhancement of carbon monoxide above background (PM/ΔCO) at Bermuda was used to estimate the degree of aerosol loss during transport to Bermuda. Results for December-February (DJF) show that most trajectories come from North America and have the highest APTs, resulting in a significant reduction (by 53 %) in PM/ΔCO under high-APT conditions (> 13.5 mm) relative to low-APT conditions (< 0.9 mm). Moreover, PM/ΔCO was most sensitive to increases in APT up to 5 mm (-0.044 μg m ppbv mm) and less sensitive to increases in APT over 5 mm. While anthropogenic PM constituents (e.g., black carbon, sulfate, organic carbon) decrease with high APT, sea salt, in contrast, was comparable between high- and low-APT conditions owing to enhanced local wind and sea salt emissions in high-APT conditions. The greater sensitivity of the fine-mode volume concentrations (versus coarse mode) to wet scavenging is evident from AErosol RObotic NETwork (AERONET) volume size distribution data. A combination of GEOS-Chem model simulations of the Pb submicron aerosol tracer and its gaseous precursor Rn reveals that (i) surface aerosol particles at Bermuda are most impacted by wet scavenging in winter and spring (due to large-scale precipitation) with a maximum in March, whereas convective scavenging plays a substantial role in summer; and (ii) North American Rn tracer emissions contribute most to surface Pb concentrations at Bermuda in winter (~75 %-80 %), indicating that air masses arriving at Bermuda experience large-scale precipitation scavenging while traveling from North America. A case study flight from the ACTIVATE field campaign on 22 February 2020 reveals a significant reduction in aerosol number and volume concentrations during air mass transport off the US East Coast associated with increased cloud fraction and precipitation. These results highlight the sensitivity of remote marine boundary layer aerosol characteristics to precipitation along trajectories, especially when the air mass source is continental outflow from polluted regions like the US East Coast.

摘要

北美洲的污染物外流在北大西洋西部无处不在,尤其是在冬季,这使得该地区成为研究降水对气团轨迹上气溶胶颗粒影响的合适天然实验室。我们利用在百慕大收集的观测数据,季节性地评估气溶胶质量浓度和体积粒径分布对轨迹累积降水量(APT)的敏感性。用百慕大气动力学直径小于2.5μm的颗粒物质量浓度除以一氧化碳高于背景值的增量(PM/ΔCO)来估算输送到百慕大期间气溶胶的损失程度。12月至2月(DJF)的结果表明,大多数轨迹来自北美洲且APT最高,在高APT条件(>13.5毫米)下,相对于低APT条件(<0.9毫米),PM/ΔCO显著降低(降低53%)。此外,PM/ΔCO对APT增加至5毫米最为敏感(-0.044微克·米-3/ppbv·毫米),对APT超过5毫米的增加不太敏感。虽然人为源PM成分(如黑碳、硫酸盐、有机碳)在高APT时减少,但相比之下,海盐在高APT和低APT条件下相当,这是由于高APT条件下当地风和海盐排放增强。从气溶胶机器人网络(AERONET)的体积粒径分布数据可以明显看出,细模态体积浓度(相对于粗模态)对湿清除更为敏感。对铅亚微米气溶胶示踪剂及其气态前体氡的GEOS-Chem模型模拟结果表明:(i)百慕大的地表气溶胶颗粒在冬季和春季(由于大规模降水)受湿清除影响最大,3月达到最大值,而对流清除在夏季起重要作用;(ii)北美洲的氡示踪剂排放对冬季百慕大地表铅浓度的贡献最大(约75%-80%),这表明到达百慕大的气团在从北美洲传输过程中经历了大规模降水清除。2020年2月22日ACTIVATE实地考察的一次案例研究飞行表明,在美国东海岸外的气团传输过程中,随着云量分数和降水量增加,气溶胶数量和体积浓度显著降低。这些结果突出了偏远海洋边界层气溶胶特征对轨迹降水的敏感性,特别是当气团源是来自美国东海岸等污染地区的大陆外流时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94a5/8609468/44d3eb401b3b/nihms-1754081-f0001.jpg

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