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

IF 3 4区 地球科学 Q2 ENVIRONMENTAL SCIENCES Journal of Atmospheric Chemistry Pub Date : 2021-10-11 DOI:10.1007/s10874-021-09427-8
Shui-Ping Wu, Xiang Li, Yang Gao, Mei-Jun Cai, Chao Xu, James J. Schwab, Chung-Shin Yuan
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引用次数: 4

摘要

2018年3月至2020年6月,在中国厦门湾沿海城市站点,使用大容量MOUDI采样器收集了大小分离的气溶胶颗粒,以研究气溶胶和水溶性无机离子(WSIIs)的季节特征以及氮种的干沉积。研究期间,PM1、PM2.5、PM10和TSP的年平均浓度分别为14.8±5.6、21.1±9.0、35.4±14.2和45.2±21.3 μ m−3。气溶胶浓度的季节变化受季风的影响,夏季最低,其他季节较高。WSIIs PM1、PM1-2.5、PM2.5-10和PM>10的年平均浓度分别为6.3±3.3、2.1±1.2、3.3±1.5和1.6±0.8 μg m−3。PM1和PM1-2.5的WSIIs浓度在春冬季最高,夏季最低。粒径分布表明,SO42−、NH4+和K+在亚微米颗粒中一致存在,Ca2+、Mg2+、Na+和Cl−主要聚集在2.5 ~ 10 μm范围内,反映了它们的优势来源不同。春、秋、冬季NO3−呈2.5-10 μm和0.44-1 μm的双峰分布。在夏季,细模态峰值消失,可能与NH4NO3形成的不利条件有关。NH4+和SO42−的优势峰在夏秋季为0.25 ~ 0.44 μm,春冬季为0.44 μm;虽然NO3-N浓度低于NH4-N,但NO3-N的干沉降通量(35.77±24.49 μmol N m−2 d−1)远高于NH4-N(10.95±11.89 μmol N m−2 d−1),这主要是由于NO3-N的沉降速度更大。海盐颗粒对总无机氮沉降的贡献率为23.9 ~ 52.8%。干沉降颗粒无机氮占其他陆地氮流入的0.95%。年总氮沉降可创造3.55 mgC m−2 d−1的新生产力,占厦门湾初级生产力的1.3 ~ 4.7%。根据这些结果,大气氮沉降可能对沿海地区人类活动源排放预计增加的营养物生物地球化学循环产生重大影响。
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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.

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来源期刊
Journal of Atmospheric Chemistry
Journal of Atmospheric Chemistry 地学-环境科学
CiteScore
4.60
自引率
5.00%
发文量
16
审稿时长
7.5 months
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.
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