Shui-Ping Wu, Xiang Li, Yang Gao, Mei-Jun Cai, Chao Xu, James J. Schwab, Chung-Shin Yuan
{"title":"厦门湾大气气溶胶中水溶性无机氮的粒径分布和干沉降通量","authors":"Shui-Ping Wu, Xiang Li, Yang Gao, Mei-Jun Cai, Chao Xu, James J. Schwab, Chung-Shin Yuan","doi":"10.1007/s10874-021-09427-8","DOIUrl":null,"url":null,"abstract":"<div><p>Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM<sub>1</sub>, PM<sub>2.5</sub>, PM<sub>10</sub>, and TSP were 14.8 ± 5.6, 21.1 ± 9.0, 35.4 ± 14.2 μg m<sup>−3</sup>, and 45.2 ± 21.3 μg m<sup>−3</sup>, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3 ± 3.3, 2.1 ± 1.2, 3.3 ± 1.5, and 1.6 ± 0.8 μg m<sup>−3</sup> in PM<sub>1</sub>, PM<sub>1-2.5</sub>, PM<sub>2.5–10</sub>, and PM<sub>>10</sub>, respectively. In addition, pronounced seasonal variations of WSIIs in PM<sub>1</sub> and PM<sub>1-2.5</sub> were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO<sub>4</sub><sup>2−</sup>, NH<sub>4</sub><sup>+</sup> and K<sup>+</sup> were consistently present in the submicron particles while Ca<sup>2+</sup>, Mg<sup>2+</sup>, Na<sup>+</sup> and Cl<sup>−</sup> mainly accumulated in the size range of 2.5–10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO<sub>3</sub><sup>−</sup> was observed with one peak at 2.5–10 μm and another peak at 0.44–1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH<sub>4</sub>NO<sub>3</sub>. For NH<sub>4</sub><sup>+</sup> and SO<sub>4</sub><sup>2−</sup>, their dominant peak at 0.25–0.44 μm in summer and fall shifted to 0.44–1 μm in spring and winter. Although the concentration of NO<sub>3</sub>–N was lower than NH<sub>4</sub>–N, the dry deposition flux of NO<sub>3</sub>–N (35.77 ± 24.49 μmol N m<sup>−2</sup> d<sup>−1</sup>) was much higher than that of NH<sub>4</sub>–N (10.95 ± 11.89 μmol N m<sup>−2</sup> d<sup>−1</sup>), mainly due to the larger deposition velocities of NO<sub>3</sub>–N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9—52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m<sup>−2</sup> d<sup>−1</sup>, accounting for 1.3–4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.</p></div>","PeriodicalId":611,"journal":{"name":"Journal of Atmospheric Chemistry","volume":"79 1","pages":"17 - 38"},"PeriodicalIF":3.0000,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10874-021-09427-8.pdf","citationCount":"4","resultStr":"{\"title\":\"Size distributions and dry deposition fluxes of water-soluble inorganic nitrogen in atmospheric aerosols in Xiamen Bay, China\",\"authors\":\"Shui-Ping Wu, Xiang Li, Yang Gao, Mei-Jun Cai, Chao Xu, James J. Schwab, Chung-Shin Yuan\",\"doi\":\"10.1007/s10874-021-09427-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM<sub>1</sub>, PM<sub>2.5</sub>, PM<sub>10</sub>, and TSP were 14.8 ± 5.6, 21.1 ± 9.0, 35.4 ± 14.2 μg m<sup>−3</sup>, and 45.2 ± 21.3 μg m<sup>−3</sup>, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3 ± 3.3, 2.1 ± 1.2, 3.3 ± 1.5, and 1.6 ± 0.8 μg m<sup>−3</sup> in PM<sub>1</sub>, PM<sub>1-2.5</sub>, PM<sub>2.5–10</sub>, and PM<sub>>10</sub>, respectively. In addition, pronounced seasonal variations of WSIIs in PM<sub>1</sub> and PM<sub>1-2.5</sub> were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO<sub>4</sub><sup>2−</sup>, NH<sub>4</sub><sup>+</sup> and K<sup>+</sup> were consistently present in the submicron particles while Ca<sup>2+</sup>, Mg<sup>2+</sup>, Na<sup>+</sup> and Cl<sup>−</sup> mainly accumulated in the size range of 2.5–10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO<sub>3</sub><sup>−</sup> was observed with one peak at 2.5–10 μm and another peak at 0.44–1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH<sub>4</sub>NO<sub>3</sub>. For NH<sub>4</sub><sup>+</sup> and SO<sub>4</sub><sup>2−</sup>, their dominant peak at 0.25–0.44 μm in summer and fall shifted to 0.44–1 μm in spring and winter. Although the concentration of NO<sub>3</sub>–N was lower than NH<sub>4</sub>–N, the dry deposition flux of NO<sub>3</sub>–N (35.77 ± 24.49 μmol N m<sup>−2</sup> d<sup>−1</sup>) was much higher than that of NH<sub>4</sub>–N (10.95 ± 11.89 μmol N m<sup>−2</sup> d<sup>−1</sup>), mainly due to the larger deposition velocities of NO<sub>3</sub>–N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9—52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m<sup>−2</sup> d<sup>−1</sup>, accounting for 1.3–4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.</p></div>\",\"PeriodicalId\":611,\"journal\":{\"name\":\"Journal of Atmospheric Chemistry\",\"volume\":\"79 1\",\"pages\":\"17 - 38\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2021-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s10874-021-09427-8.pdf\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Atmospheric Chemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10874-021-09427-8\",\"RegionNum\":4,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Atmospheric Chemistry","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s10874-021-09427-8","RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Size distributions and dry deposition fluxes of water-soluble inorganic nitrogen in atmospheric aerosols in Xiamen Bay, China
Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM1, PM2.5, PM10, and TSP were 14.8 ± 5.6, 21.1 ± 9.0, 35.4 ± 14.2 μg m−3, and 45.2 ± 21.3 μg m−3, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3 ± 3.3, 2.1 ± 1.2, 3.3 ± 1.5, and 1.6 ± 0.8 μg m−3 in PM1, PM1-2.5, PM2.5–10, and PM>10, respectively. In addition, pronounced seasonal variations of WSIIs in PM1 and PM1-2.5 were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO42−, NH4+ and K+ were consistently present in the submicron particles while Ca2+, Mg2+, Na+ and Cl− mainly accumulated in the size range of 2.5–10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO3− was observed with one peak at 2.5–10 μm and another peak at 0.44–1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH4NO3. For NH4+ and SO42−, their dominant peak at 0.25–0.44 μm in summer and fall shifted to 0.44–1 μm in spring and winter. Although the concentration of NO3–N was lower than NH4–N, the dry deposition flux of NO3–N (35.77 ± 24.49 μmol N m−2 d−1) was much higher than that of NH4–N (10.95 ± 11.89 μmol N m−2 d−1), mainly due to the larger deposition velocities of NO3–N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9—52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m−2 d−1, accounting for 1.3–4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.
期刊介绍:
The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics:
Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only.
The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere.
Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere.
Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.