Composition, isotopic fingerprint and source attribution of nitrate deposition from rain and fog at a Sub-Arctic Mountain site in Central Sweden (Mt Åreskutan)

Carmen P. Vega, E. Monica Mårtensson, U. Wideqvist, J. Kaiser, P. Zieger, J. Ström
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引用次数: 5

Abstract

Abstract While dry and rain deposition of nitrate (NO3−) and ammonium (NH4+) are regularly assessed, fog deposition is often overlooked. This work assesses summer fog events contribution to nitrogen deposition and availability for forest ecosystems. Rain and fog samples were collected at Mt Åreskutan, Sweden, during CAEsAR (Cloud and Aerosol Characterization Experiment), in 2014. NH4+ + NO3− represent (31 ± 25) % of total rain ion amount, and (31 ± 42) % in fog. Based on ion concentrations and the nitrate stable isotope signatures δ(15N) and δ(18O), it was possible to detect the plume generated by the Västmanland forest fire; NOx emissions from oil rigs and Kola Peninsula; and the plume of Bardarbunga volcano, Iceland. Scavenging of ions by fog was more efficient than by rain. Rain NH4+ and NO3− deposition was (26 ± 36) μmol m−2 d−1 and (23 ± 27) μmol m−2 d−1, respectively. Fog NH4+ and NO3− contributed (77 ± 80) % to total wet deposition of these species. Upscaling rain deposition fluxes to 1 year gave an inorganic nitrogen deposition of (18 ± 16) mmol m−2 a−1 ((252 ± 224) mg m−2 a−1 N equivalents), whereas fog deposition was estimated as (59 ± 47) mmol m−2 a−1 ((826 ± 658) mg m−2 a−1 N equivalents). Annual fog deposition was four times higher than previously reported for the area which only considered rain deposition. However, great uncertainty on the calculation of fog deposition need to be bear in mind. These findings suggest that fog should be considered in deposition estimates of inorganic nitrogen and major ions. If fog deposition is not accounted for, ion wet deposition may be greatly underestimated. Further sampling of wet and dry deposition is important for understanding the influence of nitrogen deposition on forest and vegetation development, as well as soil major ion loads.
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瑞典中部亚北极山区(Åreskutan山)雨和雾中硝酸盐沉积的组成、同位素指纹和来源归属
硝态氮(NO3−)和铵态氮(NH4+)的干沉降和雨沉降经常被评估,而雾沉降往往被忽视。这项工作评估了夏季雾事件对氮沉积和森林生态系统可用性的贡献。2014年CAEsAR(云和气溶胶表征实验)期间在瑞典Åreskutan山收集了雨和雾样本。NH4+ + NO3−占雨离子总量的(31±25)%,雾离子总量的(31±42)%。根据离子浓度和硝酸盐稳定同位素特征δ(15N)和δ(18O),可以检测Västmanland森林火灾产生的羽流;石油钻井平台和科拉半岛的氮氧化物排放;以及冰岛巴尔达邦加火山的羽流。雾对离子的清除比雨更有效。NH4+和NO3−沉积量分别为(26±36)μmol m−2 d−1和(23±27)μmol m−2 d−1。雾NH4+和NO3−对这些物种的总湿沉降贡献了(77±80)%。将降雨沉降通量升级到1年,得到的无机氮沉降为(18±16)mmol m−2 a−1((252±224)mg m−2 a−1 N当量),而雾沉降估计为(59±47)mmol m−2 a−1((826±658)mg m−2 a−1 N当量)。在只考虑降雨的地区,年雾沉降量是以前报告的四倍。但是,雾积计算的不确定性很大,需要考虑到。这些发现表明,在估计无机氮和主要离子的沉积时应考虑雾。如果不考虑雾沉积,离子湿沉积可能会被大大低估。进一步的干湿沉降取样对于了解氮沉降对森林和植被发育的影响以及土壤主要离子负荷具有重要意义。
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