Evidence for persistent organic pollutants released from melting glacier in the central Tibetan Plateau, China

2017 ◽  
Vol 220 ◽  
pp. 178-185 ◽  
Author(s):  
Jun Li ◽  
Guo-Li Yuan ◽  
Ming-Zhe Wu ◽  
Yong Sun ◽  
Peng Han ◽  
...  
2016 ◽  
Author(s):  
Jiao Ren ◽  
Xiaoping Wang ◽  
Chuanfei Wang ◽  
Ping Gong ◽  
Tandong Yao

Abstract. Atmospheric processes (air-surface exchange, and atmospheric deposition and degradation) are crucial for understanding the global cycling and fate of persistent organic pollutants (POPs). However, such assessment over the Tibetan Plateau (TP) remains uncertain. More than 50 % of the Chinese lakes are located on the TP, which exerts a remarkable influence on the regional water, energy, and chemical cycling. In this study, air and water samples were simultaneously collected in Nam Co, a large lake on the TP, to test whether the lake is a "secondary source" or "sink" of POPs. Lower concentrations of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were observed in the atmosphere and lake water of Nam Co, while the levels of polycyclic aromatic hydrocarbons (PAHs) were relatively higher. Results of fugacity ratios and chiral signatures both suggest that the lake acted as the net sink of atmospheric hexachlorocyclohexanes (HCHs), following their long-range transport driven by the Indian Monsoon. Different behaviors were observed in the PAHs, which primarily originated from local biomass burning. Acenaphthylene, acenaphthene, and fluorene showed volatilization from the lake to the atmosphere; while other PAHs were deposited into the lake due to the integrated deposition process (wet/dry and air-water gas deposition) and limited atmospheric degradation. As the dominant PAH compound, phenanthrene exhibited a seasonal reversal of air-water gas exchange, which was likely related to the melting of the lake ice in May. The annual input of HCHs from air to the entire lake area (2015 km2) was estimated as 1.9 kg year−1, while those estimated for PAHs can potentially reach up to 550 kg year−1. This study highlights the significance of PAH deposition on the regional carbon cycling in the oligotrophic lakes of the TP.


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.


2016 ◽  
Vol 16 (11) ◽  
pp. 6901-6911 ◽  
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 polystyrene–divinylbenzene copolymer resin (XAD)-based passive air samplers (PASs) 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 years 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 ongoing usage of DDT in India. This paper demonstrates the possibility of using POP fingerprints to investigate the climate interactions and the validity of using PAS to derive inter-annual atmospheric POP time trends.


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