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来自喜马拉雅山脉中部高海拔站点长期高分辨率测量的碳质气溶胶特性:辐射强迫估算以及气象和生物质燃烧的作用。

Characteristics of carbonaceous aerosols derived from long-term high-resolution measurements at a high-altitude site in the central Himalayas: radiative forcing estimates and role of meteorology and biomass burning.

机构信息

Aryabhatta Research Institute for Observational Sciences (ARIES), Manora Peak, Nainital, India.

Department of Physics and Astrophysics, University of Delhi, Delhi, India.

出版信息

Environ Sci Pollut Res Int. 2021 Mar;28(12):14654-14670. doi: 10.1007/s11356-020-11579-1. Epub 2020 Nov 20.

Abstract

Simultaneous observations (2014-2017) of organic carbon (OC) and elemental carbon (EC) are made over a high-altitude site (Nainital, 29.4°N, 79.5°E, 1958 m a.m.s.l) in the central Himalayas, and the role of long-range transport, meteorology and biomass burning is studied. There are only a few online and simultaneous observations of OC and EC over South Asia and none in the high-altitude Himalayan region. This work presents the first diurnal variations with a unimodal pattern in both OC and EC at the Himalayan site. Such a diurnal pattern is in contrast with the bimodal pattern observed at any continental polluted site. Clear seasonal variations in OC and EC were seen with a primary maximum during spring and a secondary maximum in autumn/winter. OC and EC concentrations are observed to be as high as 65.8 μg/m and 12 μg/m, in May, respectively. Concentration weighted trajectory (CWT)-assisted analysis shows that the biomass burning in northern India is one of the major sources for the springtime maximum even at this high-altitude site. The coinciding rise in OC/EC ratio from 4.6 to 7.9, along with fire events, further convinces that the enhancement in the concentrations is due to the biomass burning at distant regions and long-range transport of air masses influencing this high-altitude site. A poor covariation between OC-EC and the boundary-layer height during autumn and winter suggests that secondary maxima in OC and EC are most likely due to local sources, e.g. household burning for heating during this cold period when the temperature drops sharply after October and remains low until February. The higher temporal resolution of online measurements reveals that swiftly varying meteorological parameters change the OC-EC concentrations at diurnal scales. Back-air trajectory-assisted analysis of residence time and its relationship with OC and EC confirms the increase in their concentration in slow-moving air masses. The observed diurnal variations of EC are utilized to estimate the radiative forcing and shown that the atmospheric radiative forcing during the afternoon is about 70% higher than the forenoon one. It is envisaged that this dataset with diurnal observations of OC and EC would be an important input for studying the radiation budget and source apportionment over this high-altitude region.

摘要

在喜马拉雅山脉的一个高海拔站点(印度北阿坎德邦的奈尼塔尔,北纬 29.4°,东经 79.5°,海拔 1958 米)进行了有机碳(OC)和元素碳(EC)的同步观测(2014-2017 年),研究了长程传输、气象和生物质燃烧的作用。南亚仅有少数在线和同步的 OC 和 EC 观测,而在高海拔喜马拉雅地区则没有。本研究首次报道了喜马拉雅站点 OC 和 EC 的日变化呈单峰模式。这种日变化模式与任何大陆污染站点观察到的双峰模式形成鲜明对比。OC 和 EC 呈现明显的季节性变化,春夏季出现主要峰值,秋冬季出现次要峰值。5 月份 OC 和 EC 的浓度分别高达 65.8μg/m 和 12μg/m。浓度加权轨迹(CWT)辅助分析表明,即使在这个高海拔站点,印度北部的生物质燃烧也是春季最大值的主要来源之一。OC/EC 比值从 4.6 上升到 7.9,与火灾事件同时发生,进一步证明浓度的增加是由于远距离地区的生物质燃烧和影响这个高海拔站点的大气团长程传输。秋季和冬季 OC-EC 与边界层高度的较差协变表明,OC 和 EC 的次峰值很可能是由于本地源造成的,例如 10 月后温度急剧下降并持续到 2 月的寒冷时期,家庭取暖导致的燃烧。在线测量的更高时间分辨率揭示了迅速变化的气象参数在日尺度上改变 OC-EC 浓度。后向轨迹辅助的停留时间分析及其与 OC 和 EC 的关系证实了在缓慢移动的大气团中浓度的增加。观测到的 EC 日变化用于估算辐射强迫,并表明下午的大气辐射强迫比上午高约 70%。预计该数据集具有 OC 和 EC 的日变化观测结果,将成为研究该高海拔地区辐射预算和源分配的重要输入。

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