MIPAS 观测到的对流层上层污染物:地理和季节变化

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES Atmospheric Chemistry and Physics Pub Date : 2024-06-20 DOI:10.5194/egusphere-2024-1793
Norbert Glatthor, Gabriele P. Stiller, Thomas von Clarmann, Bernd Funke, Sylvia Kellmann, Andrea Linden
{"title":"MIPAS 观测到的对流层上层污染物:地理和季节变化","authors":"Norbert Glatthor, Gabriele P. Stiller, Thomas von Clarmann, Bernd Funke, Sylvia Kellmann, Andrea Linden","doi":"10.5194/egusphere-2024-1793","DOIUrl":null,"url":null,"abstract":"<strong>Abstract.</strong> We present a global climatology of upper tropospheric hydrogen cyanide (HCN), carbon monoxide (CO), acetylene (C<sub>2</sub>H<sub>2</sub>), ethane (C<sub>2</sub>H<sub>6</sub>), peroxyacetyl nitrate (PAN) and formic acid (HCOOH), obtained from MIPAS/Envisat observations between 2002 and 2012. At northern mid- and high latitudes the biomass burning tracer HCN as well as CO, PAN and HCOOH exhibit maxima during spring and/or summer and minima during winter. On the contrary, maximum northern extra-tropical C<sub>2</sub>H<sub>2</sub> and C<sub>2</sub>H<sub>6</sub> amounts were measured during winter and spring and minimum values during summer and fall. In the tropics and subtropics, enhanced amounts of all pollutants were observed during all seasons, especially widespread and up to southern mid-latitudes during austral spring. Other characteristic features are eastward transport of anthropogenic C<sub>2</sub>H<sub>6</sub> and of biogenic HCOOH from Central and North America in boreal summer, accumulation of pollutants in the Asian Monsoon Anticyclone and enhanced C<sub>2</sub>H<sub>2</sub> over South-East Asia in boreal winter. Clear indication of biogenic release of HCOOH was also found above tropical South America and Africa. A global correlation analysis of the other pollutants with HCN corroborates common release by biomass burning as source of the widespread southern hemispheric pollution during austral spring. Further, high correlation with HCN points to biomass burning as major source of tropical and subtropical C<sub>2</sub>H<sub>2</sub> and PAN during most of the year. In the northern extra-tropics there are generally low correlations with HCN during spring and early summer, indicating the influence of anthropogenic and biogenic sources. However, in August there are stronger correlations above Siberia and boreal North America, which points to common release by boreal fires. This is confirmed by the respective enhancement ratios (ERs). The ERs measured above North-East Africa fit well to the emission ratios of the dominant local fire type (savanna burning) for C<sub>2</sub>H<sub>2</sub>, while those for CO, C<sub>2</sub>H<sub>6</sub> and HCOOH rather indicate tropical forest fires or additional anthropogenic or biogenic sources. The southern hemispheric ΔC<sub>2</sub>H<sub>6</sub>/ΔHCN ERs obtained during August to October are in good agreement with the emission ratio for savanna fires. The same applies for ΔC<sub>2</sub>H<sub>2</sub>/ΔHCN in August and for ΔHCN/ΔCO as well as for ΔHCOOH/ΔHCN in October.","PeriodicalId":8611,"journal":{"name":"Atmospheric Chemistry and Physics","volume":"12 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Upper tropospheric pollutants observed by MIPAS: geographic and seasonal variations\",\"authors\":\"Norbert Glatthor, Gabriele P. Stiller, Thomas von Clarmann, Bernd Funke, Sylvia Kellmann, Andrea Linden\",\"doi\":\"10.5194/egusphere-2024-1793\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<strong>Abstract.</strong> We present a global climatology of upper tropospheric hydrogen cyanide (HCN), carbon monoxide (CO), acetylene (C<sub>2</sub>H<sub>2</sub>), ethane (C<sub>2</sub>H<sub>6</sub>), peroxyacetyl nitrate (PAN) and formic acid (HCOOH), obtained from MIPAS/Envisat observations between 2002 and 2012. At northern mid- and high latitudes the biomass burning tracer HCN as well as CO, PAN and HCOOH exhibit maxima during spring and/or summer and minima during winter. On the contrary, maximum northern extra-tropical C<sub>2</sub>H<sub>2</sub> and C<sub>2</sub>H<sub>6</sub> amounts were measured during winter and spring and minimum values during summer and fall. In the tropics and subtropics, enhanced amounts of all pollutants were observed during all seasons, especially widespread and up to southern mid-latitudes during austral spring. Other characteristic features are eastward transport of anthropogenic C<sub>2</sub>H<sub>6</sub> and of biogenic HCOOH from Central and North America in boreal summer, accumulation of pollutants in the Asian Monsoon Anticyclone and enhanced C<sub>2</sub>H<sub>2</sub> over South-East Asia in boreal winter. Clear indication of biogenic release of HCOOH was also found above tropical South America and Africa. A global correlation analysis of the other pollutants with HCN corroborates common release by biomass burning as source of the widespread southern hemispheric pollution during austral spring. Further, high correlation with HCN points to biomass burning as major source of tropical and subtropical C<sub>2</sub>H<sub>2</sub> and PAN during most of the year. In the northern extra-tropics there are generally low correlations with HCN during spring and early summer, indicating the influence of anthropogenic and biogenic sources. However, in August there are stronger correlations above Siberia and boreal North America, which points to common release by boreal fires. This is confirmed by the respective enhancement ratios (ERs). The ERs measured above North-East Africa fit well to the emission ratios of the dominant local fire type (savanna burning) for C<sub>2</sub>H<sub>2</sub>, while those for CO, C<sub>2</sub>H<sub>6</sub> and HCOOH rather indicate tropical forest fires or additional anthropogenic or biogenic sources. The southern hemispheric ΔC<sub>2</sub>H<sub>6</sub>/ΔHCN ERs obtained during August to October are in good agreement with the emission ratio for savanna fires. The same applies for ΔC<sub>2</sub>H<sub>2</sub>/ΔHCN in August and for ΔHCN/ΔCO as well as for ΔHCOOH/ΔHCN in October.\",\"PeriodicalId\":8611,\"journal\":{\"name\":\"Atmospheric Chemistry and Physics\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2024-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atmospheric Chemistry and Physics\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.5194/egusphere-2024-1793\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Chemistry and Physics","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.5194/egusphere-2024-1793","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

摘要我们介绍了对流层上层氰化氢(HCN)、一氧化碳(CO)、乙炔(C2H2)、乙烷(C2H6)、过氧乙酰硝酸(PAN)和甲酸(HCOOH)的全球气候学数据,这些数据来自 2002 年至 2012 年期间的 MIPAS/Envisat 观测。在北部中高纬度地区,生物质燃烧示踪剂 HCN 以及 CO、PAN 和 HCOOH 在春季和/或夏季达到最大值,在冬季达到最小值。相反,北热带外的 C2H2 和 C2H6 量在冬季和春季达到最大值,在夏季和秋季达到最小值。在热带和亚热带地区,所有污染物的含量在各个季节都有所增加,尤其是在大范围内,直至南半球中纬度地区的春季。其他特征包括:在北方夏季,人为 C2H6 和生物源 HCOOH 从中美洲和北美洲向东迁移;在亚洲季风反气旋中污染物累积;在北方冬季,东南亚上空的 C2H2 增加。在热带南美洲和非洲上空也发现了 HCOOH 生物源释放的明显迹象。对其他污染物与 HCN 的全球相关性分析证实,生物质燃烧的共同释放是南半球春季大范围污染的来源。此外,与 HCN 的高度相关性表明,生物质燃烧是全年大部分时间热带和亚热带 C2H2 和 PAN 的主要来源。在北热带以外地区,春季和初夏与 HCN 的相关性普遍较低,表明人为和生物源的影响。然而,在八月份,西伯利亚和北美洲北部上空的相关性较强,这表明北半球的火星共同释放了HCN。各自的增强比(ER)证实了这一点。在非洲东北部上空测量到的增强比与当地主要火山类型(热带稀树草原燃烧)的 C2H2 排放比非常吻合,而 CO、C2H6 和 HCOOH 的增强比则表明是热带森林火山或其他人为或生物源造成的。8 月至 10 月期间获得的南半球 ΔC2H6/ΔHCN ER 与热带稀树草原焚烧的排放比率非常吻合。8 月份的 ΔC2H2/ΔHCN 和 10 月份的 ΔHCN/ΔCO 以及 ΔHCOOH/ΔHCN 也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Upper tropospheric pollutants observed by MIPAS: geographic and seasonal variations
Abstract. We present a global climatology of upper tropospheric hydrogen cyanide (HCN), carbon monoxide (CO), acetylene (C2H2), ethane (C2H6), peroxyacetyl nitrate (PAN) and formic acid (HCOOH), obtained from MIPAS/Envisat observations between 2002 and 2012. At northern mid- and high latitudes the biomass burning tracer HCN as well as CO, PAN and HCOOH exhibit maxima during spring and/or summer and minima during winter. On the contrary, maximum northern extra-tropical C2H2 and C2H6 amounts were measured during winter and spring and minimum values during summer and fall. In the tropics and subtropics, enhanced amounts of all pollutants were observed during all seasons, especially widespread and up to southern mid-latitudes during austral spring. Other characteristic features are eastward transport of anthropogenic C2H6 and of biogenic HCOOH from Central and North America in boreal summer, accumulation of pollutants in the Asian Monsoon Anticyclone and enhanced C2H2 over South-East Asia in boreal winter. Clear indication of biogenic release of HCOOH was also found above tropical South America and Africa. A global correlation analysis of the other pollutants with HCN corroborates common release by biomass burning as source of the widespread southern hemispheric pollution during austral spring. Further, high correlation with HCN points to biomass burning as major source of tropical and subtropical C2H2 and PAN during most of the year. In the northern extra-tropics there are generally low correlations with HCN during spring and early summer, indicating the influence of anthropogenic and biogenic sources. However, in August there are stronger correlations above Siberia and boreal North America, which points to common release by boreal fires. This is confirmed by the respective enhancement ratios (ERs). The ERs measured above North-East Africa fit well to the emission ratios of the dominant local fire type (savanna burning) for C2H2, while those for CO, C2H6 and HCOOH rather indicate tropical forest fires or additional anthropogenic or biogenic sources. The southern hemispheric ΔC2H6/ΔHCN ERs obtained during August to October are in good agreement with the emission ratio for savanna fires. The same applies for ΔC2H2/ΔHCN in August and for ΔHCN/ΔCO as well as for ΔHCOOH/ΔHCN in October.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Atmospheric Chemistry and Physics
Atmospheric Chemistry and Physics 地学-气象与大气科学
CiteScore
10.70
自引率
20.60%
发文量
702
审稿时长
6 months
期刊介绍: Atmospheric Chemistry and Physics (ACP) is a not-for-profit international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth''s atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere. The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions. The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.
期刊最新文献
Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean Identifying decadal trends in deweathered concentrations of criteria air pollutants in Canadian urban atmospheres with machine learning approaches The water-insoluble organic carbon in PM2.5 of typical Chinese urban areas: light-absorbing properties, potential sources, radiative forcing effects, and a possible light-absorbing continuum Using a region-specific ice-nucleating particle parameterization improves the representation of Arctic clouds in a global climate model Evaluation of modelled versus observed non-methane volatile organic compounds at European Monitoring and Evaluation Programme sites in Europe
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1