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Seasonal variation and spatial distribution of carbonaceous aerosols in Taiwan

机译:台湾碳质气溶胶的季节变化与空间分布

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摘要

To investigate the physico-chemical properties of aerosols in Taiwan, an observation network was initiated in 2003. In this work, the measurements of the mass concentration and carbonaceous composition of PM10 and PM2.5 are presented. Analysis on the data collected in the first 5-years, from 2003 to 2007, showed that there was a very strong contrast in the aerosol concentration and composition between the rural and the urban/suburban stations. The five-year means of EC at the respective stations ranged from 0.9±0.04 to 4.2±0.1 μgC mg~(-3). In rural areas, EC accounted for 2-3% of PM10 and 3-5% of PM2.5 mass loadings, comparing to 4-6% of PM10 and 4-8% of PM2.5 in the urban areas. It was found that the spatial distribution of EC was consistent with CO and NOx across the network stations, suggesting that the levels of EC over Taiwan were dominated by local sources. The measured OC was split into POC and SOC counterparts following the EC tracer method. Five-year means of POC ranged from 1.8±0.1 to 9.7±0.2 μgC mg~(-3) among the stations. It was estimated that the POM contributed 5-17% of PM10 and 7-18% of PM2.5 in Taiwan. On the other hand, the five-year means of SOC ranged from 1.5±0.1 to 3.8±.3 μgC mg~(-3). The mass fractions of SOM were estimated to be 9-19% in PM10 and 14-22% in PM2.5. The results showed that the SOC did not exhibit significant urban-rural contrast as did the POC and EC. A significant cross-station correlation between SOC and total oxidant was observed, which means the spatial distribution of SOC in Taiwan was dominated by the oxidant mixing ratio. Besides, correlation was also found between SOC and particulate nitrate, implying that the precursors of SOA were mainly from local anthropogenic sources. In addition to the spatial distribution, the carbonaceous aerosols also exhibited distinct seasonality. In northern Taiwan, the concentrations of all the three carbonaceous components (EC, POC, and SOC) reached their respective minima in the fall season. POC and EC increased drastically in winter and peaked in spring, whereas the SOC was characterized by a bimodal pattern with the maximal concentration in winter and a second mode in summertime. In southern Taiwan, minimal levels of POC and EC occurred consistently in summer and the maxima were observed in winter, whereas the SOC peaked in summer and declined in wintertime. The discrepancies in the seasonality of carbonaceous aerosols between northern and southern Taiwan were most likely caused by the seasonal meteorological settings that dominated the dispersion of air pollutants. Moreover, it was inferred that the Asian pollution outbreaks could have shifted the seasonal maxima of air pollutants from winter to spring in the northern Taiwan, and that the increases in biogenic SOA precursors and the enhancement in SOA yield were responsible for the elevated SOC concentrations in summer.
机译:为了调查台湾气溶胶的理化特性,2003年启动了一个观测网络。在这项工作中,提出了对PM10和PM2.5的质量浓度和含碳成分的测量。对从2003年到2007年的前5年收集的数据进行的分析表明,农村站点与城市/郊区站点之间的气溶胶浓度和组成存在非常强烈的对比。各站的EC的五年平均值范围为0.9±0.04至4.2±0.1μgCmg〜(-3)。在农村地区,EC占PM10的2-3%,占PM2.5的3-5%,而在城市地区,EC占PM10的4-6%和PM2.5的4-8%。发现EC的空间分布与网络中的CO和NOx一致,这表明台湾EC的水平主要由本地资源决定。按照EC示踪剂方法,将测得的OC分为POC和SOC对应物。各站间POC的五年平均值在1.8±0.1至9.7±0.2μgCmg〜(-3)之间。据估计,在台湾,POM贡献了PM10的5-17%和PM2.5的7-18%。另一方面,SOC的5年平均值范围为1.5±0.1至3.8±.3μgCmg〜(-3)。 SOM的质量分数在PM10中估计为9-19%,在PM2.5中为14-22%。结果表明,SOC没有像POC和EC那样显示出明显的城乡对比。 SOC与总氧化剂之间存在明显的跨站相关性,这意味着台湾SOC的空间分布主要由氧化剂混合比决定。此外,还发现SOC与硝酸盐颗粒之间存在相关性,这表明SOA的前体主要来自当地的人为来源。除空间分布外,碳质气溶胶还表现出明显的季节性。在台湾北部,三个碳质成分(EC,POC和SOC)的浓度在秋季都达到了各自的最小值。 POC和EC在冬季急剧增加,并在春季达到峰值,而SOC则以双峰模式为特征,冬季出现最大浓度,夏季出现第二模式。在台湾南部,POC和EC的最低水平在夏季持续出现,而在冬季则达到最大值,而SOC在夏季达到峰值,而在冬季则下降。台湾北部和南部之间碳质气溶胶的季节性差异最有可能是由支配空气污染物扩散的季节性气象环境引起的。此外,据推测,亚洲污染爆发可能使台湾北部空气污染物的季节最大值从冬季转移到春季,而生物源SOA前体的增加和SOA产量的增加是造成SOC浓度升高的原因。夏季。

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