Institute of Earth Sciences, China University of Geosciences (Beijing), Beijing 100083, China.
Institute of Earth Sciences, China University of Geosciences (Beijing), Beijing 100083, China.
Sci Total Environ. 2023 Jan 15;856(Pt 2):159234. doi: 10.1016/j.scitotenv.2022.159234. Epub 2022 Oct 6.
Anthropogenic reactive nitrogen emissions have a significant impact on atmospheric chemical composition and earth surface ecosystem. As one of the most important sinks of atmospheric nitrogen, the wet deposition of nitrate (rainwater NO) has been widely concerned. Yet, the sources and transformation processes of wet deposited NO were not well revealed in megacity during rainy season in the context of global climate change. Here, we investigated the concentrations of nitrogen components and dual isotopes of rainwater nitrate collected in Beijing during July to August 2021 (rainy season). The main findings showed that the concentrations of NH-N, NO-N, and NO-N ranged 0.5- 6.7 mg L, 0.3- 4.5 mg L, and 0.05- 0.18 mg L, respectively, with the average relative percentages of 69 %, 29 %, and 2 %. The stoichiometry analysis of characteristic ion ratios indicated that the contribution of municipal wastes and agricultural sources to rainwater NH-N is relatively significant, while traffics were the major contributor of NO-N instead of the fixed emission. Rainwater δN-NO and δO-NO presented slightly N-depleted characteristic compared to previous studies with the average values of -3.9 ± 3.1 ‰ and 58.7 ± 12.6 ‰. These isotope compositions suggesting an origin of rainwater NO from the mixing of multi-sources and was mainly generated via the pathway of OH radical oxidization. Further source apportionment of rainwater NO by Bayesian mixing model evaluated that traffic (30.3 %) and soil (30.3 %) emissions contributed mostly to NO, while the contribution of biomass burning (18.8 %) and coal combustion (20.6 %) were relatively lower. This study highlighted the important role of dual isotopes in rainwater nitrate source identification and formation processes in megacity.
人为活性氮排放对大气化学组成和地球表面生态系统有重大影响。作为大气氮的最重要汇之一,硝酸盐(雨水 NO)的湿沉降已受到广泛关注。然而,在全球气候变化背景下,有关大都市雨季雨水 NO 的来源和转化过程还没有得到很好的揭示。在这里,我们研究了 2021 年 7 月至 8 月(雨季)在北京采集的雨水氮成分和硝酸盐双同位素的浓度。主要发现表明,NH-N、NO-N 和 NO-N 的浓度范围分别为 0.5-6.7 mg/L、0.3-4.5 mg/L 和 0.05-0.18 mg/L,平均相对百分比分别为 69%、29%和 2%。特征离子比的化学计量分析表明,城市废物和农业源对雨水 NH-N 的贡献相对较大,而交通则是 NO-N 的主要来源,而不是固定排放。与之前的研究相比,雨水 δN-NO 和 δO-NO 呈现出略微的氮亏损特征,平均值分别为-3.9±3.1‰和 58.7±12.6‰。这些同位素组成表明雨水 NO 的来源是多种来源的混合,主要通过 OH 自由基氧化途径生成。贝叶斯混合模型对雨水 NO 的源分配进一步评估表明,交通(30.3%)和土壤(30.3%)排放对 NO 的贡献最大,而生物质燃烧(18.8%)和煤炭燃烧(20.6%)的贡献相对较低。本研究强调了双同位素在大都市雨水硝酸盐源识别和形成过程中的重要作用。