Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101, China.
Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101, China; CAS Center for Excellence in Tibetan Plateau Earth Sciences, Beijing, China.
Sci Total Environ. 2016 Dec 15;573:1041-1052. doi: 10.1016/j.scitotenv.2016.08.184. Epub 2016 Sep 5.
Airborne black carbon (BC) mass concentrations were measured from November 2012 to June 2013 at Ranwu and Beiluhe, located in the southeastern and central Tibetan Plateau, respectively. Monthly mean BC concentrations show a winter (November-February) high (413.2ngm) and spring (March-June) low (139.1ngm) at Ranwu, but in contrast a winter low and spring high at Beiluhe (204.8 and 621.6ngm, respectively). By examining the meteorological conditions at various scales, we found that the monthly variation of airborne BC over the southeastern Tibetan Plateau (TP) was highly influenced by regional precipitation and over the hinterland by winds. Local precipitation at both sites showed little impact on the seasonal variation of airborne BC concentrations. Potential BC source regions are identified using air mass backward trajectory analysis. At Ranwu, BC was dominated by the air masses from the northeastern India and Bangladesh in both winter and spring, whereas at Beiluhe it was largely contributed by air masses from the south slope of Himalayas in winter, and from the arid region in the north of the TP in spring. The winter and spring seasonal peak of BC in the southern TP is largely contributed by emissions from South Asia, and this seasonal variation is heavily influenced by the regional monsoon. In the northern TP, BC had high concentrations during spring and summer seasons, which is very likely associated with more efficient transport of BC over the arid regions on the north of Tibetan Plateau and in Central Asia. Airborne BC concentrations at the Ranwu sampling site showed a significant diurnal cycle with a peak shortly after sunrise followed by a decrease before noon in both winter and spring, likely shaped by local human activities and the diurnal variation of wind speed. At the Beiluhe sampling site, the diurnal variation of BC is different and less distinct.
从 2012 年 11 月到 2013 年 6 月,在分别位于青藏高原东南部和中部的然乌和北麓河两地测量了空气中的黑碳(BC)质量浓度。在然乌,BC 的月平均浓度呈现冬季(11 月至 2 月)高(413.2ng/m3)和春季(3 月至 6 月)低(139.1ng/m3)的特点,但在北麓河,情况则相反,冬季低而春季高(分别为 204.8 和 621.6ng/m3)。通过考察不同尺度的气象条件,我们发现,青藏高原东南部地区空中 BC 的月变化受区域降水影响较大,而内陆地区则受风的影响较大。两地的局地降水对空气中 BC 浓度的季节性变化影响不大。利用空气团后向轨迹分析确定了潜在的 BC 源区。在然乌,冬季和春季的 BC 主要来自印度东北部和孟加拉国的气团,而在北麓河,冬季主要来自喜马拉雅山南坡的气团,春季则主要来自青藏高原北部干旱地区的气团。南部 TP 的冬季和春季 BC 季节性峰值主要来自南亚的排放,这种季节性变化受区域季风的强烈影响。在北部 TP,BC 在春季和夏季的浓度较高,这很可能与青藏高原北部和中亚干旱地区更有效的 BC 输送有关。然乌采样点的空气中 BC 浓度呈现出显著的日变化,冬季和春季均在日出后不久达到峰值,然后在中午前下降,这可能是由当地人类活动和风速的日变化引起的。在北麓河采样点,BC 的日变化则不同,不太明显。