scholarly journals Atmospheric brown clouds reach the Tibetan Plateau by crossing the Himalayas

2015 ◽  
Vol 15 (11) ◽  
pp. 6007-6021 ◽  
Author(s):  
Z. L. Lüthi ◽  
B. Škerlak ◽  
S.-W. Kim ◽  
A. Lauer ◽  
A. Mues ◽  
...  

Abstract. The Himalayas and the Tibetan Plateau region (HTP), despite being a remote and sparsely populated area, is regularly exposed to polluted air masses with significant amounts of aerosols including black carbon. These dark, light-absorbing particles are known to exert a great melting potential on mountain cryospheric reservoirs through albedo reduction and radiative forcing. This study combines ground-based and satellite remote sensing data to identify a severe aerosol pollution episode observed simultaneously in central Tibet and on the southern side of the Himalayas during 13–19 March 2009 (pre-monsoon). Trajectory calculations based on the high-resolution numerical weather prediction model COSMO are used to locate the source regions and study the mechanisms of pollution transport in the complex topography of the HTP. We detail how polluted air masses from an atmospheric brown cloud (ABC) over South Asia reach the Tibetan Plateau within a few days. Lifting and advection of polluted air masses over the great mountain range is enabled by a combination of synoptic-scale and local meteorological processes. During the days prior to the event, winds over the Indo-Gangetic Plain (IGP) are generally weak at lower levels, allowing for accumulation of pollutants and thus the formation of ABCs. The subsequent passing of synoptic-scale troughs leads to southwesterly flow in the middle troposphere over northern and central India, carrying the polluted air masses across the Himalayas. As the IGP is known to be a hotspot of ABCs, the cross-Himalayan transport of polluted air masses may have serious implications for the cryosphere in the HTP and impact climate on regional to global scales. Since the current study focuses on one particularly strong pollution episode, quantifying the frequency and magnitude of similar events in a climatological study is required to assess the total impact.

2014 ◽  
Vol 14 (20) ◽  
pp. 28105-28146 ◽  
Author(s):  
Z. L. Lüthi ◽  
B. Škerlak ◽  
S.-W. Kim ◽  
A. Lauer ◽  
A. Mues ◽  
...  

Abstract. The Himalayas and the Tibetan Plateau region (HTP), despite being a remote and sparsely populated area, is regularly exposed to polluted air masses with significant amounts of aerosols including black carbon. These dark, light-absorbing particles are known to exert a great melting potential on mountain cryospheric reservoirs through albedo reduction and radiative forcing. This study combines the available yet sparse ground-based and satellite data to identify a severe aerosol pollution episode observed simultaneously in central Tibet and on the southern side of the Himalayas during 13–19 March 2009. We detail how polluted air masses such as an atmospheric brown cloud (ABC) over South Asia reached the Tibetan Plateau during this pre-monsoon case study. In order to address the mechanisms of pollution transport in the complex topography of the HTP, air-mass trajectories are calculated using hourly outputs from the high-resolution numerical weather prediction model COSMO. Cross-mountain pollution transport is found to occur to a large extent at elevated tropospheric levels other than just through major river valleys. Lifting and advection of polluted air masses over the great mountain range is enabled by a combination of synoptic and local meteorological settings. Winds over the Indo Gangetic Plain (IGP) are generally weak at lower levels during the event, allowing for accumulation of pollutants. The passing of synoptic-scale troughs leads to south-westerly flow in the middle troposphere over northern and central India. Thus, ABC can build up south of the Himalayas and get carried northwards across the mountain range and onto the Tibetan Plateau as the winds obtain a southerly component. Air masses from the ABC hot-spot of the IGP can reach the high glaciers, which may have serious implications for the cryosphere in the HTP region and for climate on regional to global scales.


2017 ◽  
Vol 17 (4) ◽  
pp. 3083-3095 ◽  
Author(s):  
Ruixiong Zhang ◽  
Yuhang Wang ◽  
Qiusheng He ◽  
Laiguo Chen ◽  
Yuzhong Zhang ◽  
...  

Abstract. Long-range transport followed by deposition of black carbon on glaciers of Tibet is one of the key issues of climate research as it induces changes on radiative forcing and subsequently impacting the melting of glaciers. The transport mechanism, however, is not well understood. In this study, we use short-lived reactive aromatics as proxies to diagnose transport of pollutants to Tibet. In situ observations of short-lived reactive aromatics across the Tibetan Plateau are analyzed using a regional chemistry and transport model. The model performance using the current emission inventories over the region is poor due to problems in the inventories and model transport. Top-down emissions constrained by satellite observations of glyoxal are a factor of 2–6 higher than the a priori emissions over the industrialized Indo-Gangetic Plain. Using the top-down emissions, agreement between model simulations and surface observations of aromatics improves. We find enhancements of reactive aromatics over Tibet by a factor of 6 on average due to rapid transport from India and nearby regions during the presence of a high-altitude cut-off low system. Our results suggest that the cut-off low system is a major pathway for long-range transport of pollutants such as black carbon. The modeling analysis reveals that even the state-of-the-science high-resolution reanalysis cannot simulate this cut-off low system accurately, which probably explains in part the underestimation of black carbon deposition over Tibet in previous modeling studies. Another model deficiency of underestimating pollution transport from the south is due to the complexity of terrain, leading to enhanced transport. It is therefore challenging for coarse-resolution global climate models to properly represent the effects of long-range transport of pollutants on the Tibetan environment and the subsequent consequence for regional climate forcing.


2016 ◽  
Author(s):  
Ruixiong Zhang ◽  
Yuhang Wang ◽  
Qiusheng He ◽  
Laiguo Chen ◽  
Yuzhong Zhang ◽  
...  

Abstract. Long-range transport and subsequent deposition of black carbon on glaciers of Tibet is one of the key issues of climate research inducing changes on radiative forcing and subsequently impacting on the melting of glaciers. The transport mechanism, however, is not well understood. In this study, we use short-lived reactive aromatics as proxies to diagnose transport of pollutants to Tibet. In situ observations of short-lived reactive aromatics across the Tibetan Plateau are analyzed using a regional chemistry and transport model. The model performance using the current emission inventories over the region is poor due to problems in the inventories and model transport. Top-down emissions constrained by satellite observations of glyoxal (CHOCHO) are a factor of 2–6 higher than the a priori emissions over the industrialized Indo-Gangetic Plain. Using the top-down emissions, agreement between model simulations and surface observations of aromatics improves. We find enhancements of reactive aromatics over Tibet by a factor of 6 on average due to rapid transport from India and nearby regions during the presence of a high-altitude cut-off low system. Our results suggest that the cut-off low system is a major pathway for long-range transport of pollutants such as black carbon. The modeling analysis reveals that even the state-of-the-science high-resolution reanalysis cannot simulate this cut-off low system accurately, which probably explains in part the underestimation of black carbon deposition over Tibet in previous modeling studies. Furthermore, another model deficiency of underestimating pollution transport from the south is due to the complexity of terrain, leading to enhanced transport. It is therefore challenging for coarse-resolution global climate models to properly represent the effects of long-range transport of pollutants on the Tibetan environment and the subsequent consequence for regional climate forcing.


2016 ◽  
Author(s):  
Xiaoping Wang ◽  
Jiao Ren ◽  
Ping Gong ◽  
Chuanfei Wang ◽  
Yonggang Xue ◽  
...  

Abstract. The Tibetan Plateau (TP) has been contaminated by persistent organic pollutants (POPs), including legacy organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) through atmospheric transport. The exact source regions, transport pathways and time trends of POPs to the TP are not well understood. Here XAD-based passive air samplers (PAS) were deployed at 16 Tibetan background sites from 2007 to 2012 to gain further insight into spatial patterns and temporal trends of OCPs and PCBs. The southeastern TP was characterized by dichlorodiphenyltrichloroethane (DDT) -related chemicals delivered by Indian Monsoon air masses. The northern and northwestern TP displayed the greatest absolute concentration and relative abundance of hexachlorobenzene (HCB) in the atmosphere, caused by the westerly-driven European air masses. The interactions between the DDT polluted Indian monsoon air and the clean westerly winds formed a transition zone in central Tibet where both DDT and HCB were the dominant chemicals. Based on 5-year of continuous sampling, our data indicated declining concentrations of HCB and hexachlorocyclohexanes (HCHs) across the Tibetan region. Inter-annual trends of DDT class chemicals, however, showed less variation during this 5-year sampling period, which may be due to the on-going usage of DDT in India. This paper demonstrates the possibility of using POPs fingerprints to investigate the climate interactions and the validity of using PAS to derive inter-annual atmospheric POPs time trends.


2019 ◽  
Vol 32 (4) ◽  
pp. 1181-1202 ◽  
Author(s):  
Zhiling Xie ◽  
Bin Wang

Multiple bias-corrected top-quality reanalysis datasets, gauge-based observations, and selected satellite products are synthetically employed to revisit the climatology and variability of the summer atmospheric heat sources over the Tibetan Plateau (TP). Verification-based selection and ensemble-mean methods are utilized to combine various datasets. Different from previous works, this study pays special attention to estimating the total heat source (TH) and its components over the data-void western plateau (70°–85°E), including the surface sensible heat (SH), latent heat released by precipitation (LH), and net radiation flux (RD). Consistent with previous studies, the climatology of summer SH (LH) typically increases (decreases) from southeast to northwest. Generally, LH dominates TH over most of the TP. A notable new finding is a minimum TH area over the high-altitude region of the northwestern TP, where the Karakoram mountain range is located. We find that during the period of 1984–2006, TH shows insignificant trends over the eastern and central TP, whereas it exhibits an evident increasing trend over the western TP that is attributed to the rising tendency of LH before 1996 and to that of RD after 1996. The year-to-year variation of TH over the central–eastern TP is highly correlated with that of LH, but that is not the case over the western TP. It is also worth noting that the variations of TH in each summer month are not significantly correlated with each other, and hence study of the interannual variation of the TP heat sources should consider the remarkable subseasonal variations.


2019 ◽  
Vol 19 (2) ◽  
pp. 1373-1391 ◽  
Author(s):  
Huiming Lin ◽  
Yindong Tong ◽  
Xiufeng Yin ◽  
Qianggong Zhang ◽  
Hui Zhang ◽  
...  

Abstract. Located in the world's “third pole” and a remote region connecting the Indian plate and the Eurasian plate, Qomolangma National Nature Preserve (QNNP) is an ideal region to study the long-range transport of atmospheric pollutants. In this study, gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM) and particle-bound mercury (PBM) were continuously measured during the Indian monsoon transition period in QNNP. A slight increase in the GEM concentration was observed from the period preceding the Indian summer monsoon (1.31±0.42 ng m−3) to the Indian summer monsoon period (1.44±0.36 ng m−3), while significant decreases were observed in the GOM and PBM concentrations, with concentrations decreasing from 35.2±18.6 to 19.3±10.9 pg m−3 (p < 0.001) for GOM and from 30.5±12.5 to 24.9±19.8 pg m−3 (p < 0.001) for PBM. A unique daily pattern was observed in QNNP with respect to the GEM concentration, with a peak value before sunrise and a low value at noon. Relative to the (low) GEM concentrations, GOM concentrations (with a mean value of 21.4±13.4 pg m−3, n=1239) in this region were relatively high compared with the measured values in some other regions of China. A cluster analysis indicated that the air masses transported to QNNP changed significantly at different stages of the monsoon, and the major potential mercury (Hg) sources shifted from northern India and western Nepal to eastern Nepal and Bangladesh. As there is a large area covered in glaciers in QNNP, local glacier winds could increase the transboundary transport of pollutants and transport polluted air masses to the Tibetan Plateau. The atmospheric Hg concentration in QNNP in the Indian summer monsoon period was influenced by transboundary Hg flows. This highlights the need for a more specific identification of Hg sources impacting QNNP and underscores the importance of international cooperation regarding global Hg controls.


2014 ◽  
Vol 14 (13) ◽  
pp. 7091-7112 ◽  
Author(s):  
C. He ◽  
Q. B. Li ◽  
K. N. Liou ◽  
J. Zhang ◽  
L. Qi ◽  
...  

Abstract. We systematically evaluate the black carbon (BC) simulations for 2006 over the Tibetan Plateau by a global 3-D chemical transport model (CTM) (GEOS-Chem) driven by GEOS-5 assimilated meteorological fields, using in situ measurements of BC in surface air, BC in snow, and BC absorption aerosol optical depth (AAOD). Using improved anthropogenic BC emission inventories for Asia that account for rapid technology renewal and energy consumption growth (Zhang et al., 2009; Lu et al., 2011) and improved global biomass burning emission inventories that account for small fires (van der Werf et al., 2010; Randerson et al., 2012), we find that model results of both BC in surface air and in snow are statistically in good agreement with observations (biases < 15%) away from urban centers. Model results capture the seasonal variations of the surface BC concentrations at rural sites in the Indo-Gangetic Plain, but the observed elevated values in winter are absent. Modeled surface-BC concentrations are within a factor of 2 of the observations at remote sites. Part of the discrepancy is explained by the deficiencies of the meteorological fields over the complex Tibetan terrain. We find that BC concentrations in snow computed from modeled BC deposition and GEOS-5 precipitation are spatiotemporally consistent with observations (r = 0.85). The computed BC concentrations in snow are a factor of 2–4 higher than the observations at several Himalayan sites because of excessive BC deposition. The BC concentrations in snow are biased low by a factor of 2 in the central plateau, which we attribute to the absence of snow aging in the CTM and strong local emissions unaccounted for in the emission inventories. Modeled BC AAOD is more than a factor of 2 lower than observations at most sites, particularly to the northwest of the plateau and along the southern slopes of the Himalayas in winter and spring, which is attributable in large part to underestimated emissions and the assumption of external mixing of BC aerosols in the model. We find that assuming a 50% increase of BC absorption associated with internal mixing reduces the bias in modeled BC AAOD by 57% in the Indo-Gangetic Plain and the northeastern plateau and to the northeast of the plateau, and by 16% along the southern slopes of the Himalayas and to the northwest of the plateau. Both surface BC concentration and AAOD are strongly sensitive to anthropogenic emissions (from China and India), while BC concentration in snow is especially responsive to the treatment of BC aerosol aging. We find that a finer model resolution (0.5° × 0.667° nested over Asia) reduces the bias in modeled surface-BC concentration from 15 to 2%. The large range and non-homogeneity of discrepancies between model results and observations of BC across the Tibetan Plateau undoubtedly undermine current assessments of the climatic and hydrological impact of BC in the region and thus warrant imperative needs for more extensive measurements of BC, including its concentration in surface air and snow, AAOD, vertical profile and deposition.


2016 ◽  
Vol 19 (2) ◽  
pp. 130-137
Author(s):  
Vu Hien Phan ◽  
Roderik Lindenbergh ◽  
Massimo Menenti

Monitoring glacier changes is essential for estimating the water mass balance of the Tibetan Plateau. Recent research indicates that glaciers at individual regions on the Tibetan Plateau and surroundings are shrinking and thinning during the last decades. Studies considering large regions often ignored however the impact of locally varying weather conditions and terrain characteristics on glacial evolution, i.e. the impact of orographic precipitation and variation in solar radiation. Our hypothesis is therefore that adjacent glaciers of opposite orientation change in a different way. In this study, we exploit Ice Cloud and land Elevation Satellite (ICESat)/ Geoscience Laser Altimetry System (GLAS) data in combination with the NASA Shuttle Radar Topographic Mission (SRTM) digital elevation model (DEM) and the Global Land Ice Measurements from Space (GLIMS) glacier mask to estimate glacial thickness change trends between 2003 and 2009 on the whole Tibetan Plateau. The results show that 90 glacial areas could be distinguished. Most of observed glacial areas on the Tibetan Plateau are thinning, except for some glaciers in the Northwest. In general, glacial elevations on the whole Tibetan Plateau decreased at an average rate of -0.17 ± 0.47 meters per year (m a-1) between 2003 and 2009, taking together glaciers of any size, distribution, and location of the observed glacial area. Moreover, the results show that glacial elevation changes indeed strongly depend on the relative position in a mountain range.


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