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[冬春季节东海气溶胶和雨水中的尿素]

[Urea in aerosol and rainwater over the East China Sea in winter and spring].

作者信息

Bo Shao-yi, Shi Jin-hui, Gao Hui-wang, Qi Jian-hu, Qiao Jia-jia, Zhang Jing

机构信息

Key Laboratory of Marine Environmental Science and Ecology, Ministry of Education, Ocean University of China, Qingdao 266100.

出版信息

Huan Jing Ke Xue. 2009 Jan;30(1):14-22.

Abstract

Organic nitrogen is a quantitatively important component of fixed nitrogen in atmospheric aerosol and rainwater. Urea as a possible candidate of organic nitrogen component might have a significant influence to the marine ecosystem since its bioavailability and broad range of natural and anthropogenic sources. 23 total suspended particulate samples, 4 size-segregated particles samples and 10 rainwater samples collected over the East China Sea from Nov. to Dec., 2006 and Feb. to Mar., 2007 were applied to analyze the concentrations of urea, nitrate and ammonium in aerosols and rainwater, respectively. In winter and spring, the concentrations of urea nitrogen were from 0.2 nmol m(-3) to 17.7 nmolx m(-3) and 6.5 nmol x m(-3) to 14.6 nmol x m(-3) in bulk aerosols, respectively and the corresponding concentrations were from 7.8 miromol x L(-1) to 18.1 micromol x L(-1) and 12.1 micromol x L(-1) to 35.3 micromol x L(-1) in rainwater. In both aerosols and rainwater over the East China Sea, the concentrations of urea nitrogen were higher in spring than those in winter. Urea nitrogen in aerosols contributed about 5% to the three measured nitrogen species and it was about 20% in rainwater. The size distribution of urea was markedly different from those of nitrate and ammonium,which had no pronounced difference among cascade stages. A slightly enhance urea contribution presented in the range of 0.43-0.65 microm in spring, which was 19.8%. In contrast, an enhancement presented in the range of 3.3-4.7 microm in winter, which was 19.8%. Factor analysis indicated that the sources of urea in aerosols were dominated by wind-blown soils in winter and sublime of urea in soils in spring, respectively.

摘要

有机氮是大气气溶胶和雨水中固定氮在数量上的重要组成部分。尿素作为有机氮成分的一个可能候选者,由于其生物可利用性以及广泛的自然和人为来源,可能对海洋生态系统有重大影响。2006年11月至12月以及2007年2月至3月在中国东海采集的23个总悬浮颗粒物样本、4个粒径分级颗粒物样本和10个雨水样本,分别用于分析气溶胶和雨水中尿素、硝酸盐和铵的浓度。在冬季和春季,大气气溶胶中尿素氮的浓度分别为0.2纳摩尔/立方米至17.7纳摩尔/立方米和6.5纳摩尔/立方米至14.6纳摩尔/立方米,雨水中相应的浓度分别为7.8微摩尔/升至18.1微摩尔/升和12.1微摩尔/升至35.3微摩尔/升。在中国东海的气溶胶和雨水中,春季尿素氮的浓度均高于冬季。气溶胶中的尿素氮对所测三种氮物种的贡献约为5%,而在雨水中约为20%。尿素的粒径分布与硝酸盐和铵的明显不同,硝酸盐和铵在分级阶段之间没有明显差异。春季在0.43 - 0.65微米范围内尿素贡献略有增加,为19.8%。相比之下,冬季在3.3 - 4.7微米范围内有增加,为19.8%。因子分析表明,气溶胶中尿素的来源在冬季分别以风扬尘土为主,春季以土壤中尿素的升华为主。

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