Modeling redistribution of α-HCH in Chinese soil induced by environment factors

This study explores long-term environmental fate of alpha-HCH in China from 1952 to 2007 using ChnGPERM (Chinese Gridded Pesticide Emission and Residue Model). The model captures well the temporal and spatial variations of alpha-HCH concentration in Chinese soils by comparing with a number of measured data across China in different periods. The results demonstrate alpha-HCH grasshopping effect in Eastern China and reveal several important features of the chemical in Northeast and Southeast China. It is found that Northeast China is a prominent sink region of alpha-HCH emitted from Chinese sources and alpha-HCH contamination in Southwest China is largely attributed to foreign sources. Southeast China is shown to be a major source contributing to alpha-HCH contamination in Northeast China, incurred by several environmental factors including temperature, soil organic carbon content, wind field and precipitation. (C) 2011 Elsevier Ltd. All rights reserved.This study explores long-term environmental fate of alpha-HCH in China from 1952 to 2007 using ChnGPERM (Chinese Gridded Pesticide Emission and Residue Model). The model captures well the temporal and spatial variations of alpha-HCH concentration in Chinese soils by comparing with a number of measured data across China in different periods. The results demonstrate alpha-HCH grasshopping effect in Eastern China and reveal several important features of the chemical in Northeast and Southeast China. It is found that Northeast China is a prominent sink region of alpha-HCH emitted from Chinese sources and alpha-HCH contamination in Southwest China is largely attributed to foreign sources. Southeast China is shown to be a major source contributing to alpha-HCH contamination in Northeast China, incurred by several environmental factors including temperature, soil organic carbon content, wind field and precipitation. (C) 2011 Elsevier Ltd. All rights reserved

Gridded inventories of historical usage for selected organochlorine pesticides in Gansu Province, China

HCHs and DDTs were banned in 1983 in China; however, they are still remaining in various environmental media. Since endosulfan was introduced in China in 1994, it is widely used in agriculture. In this study, temporal and spatial uses of endosulfan, HCHs, and DDTs in Gansu province of China have been presented. It is estimated that the total usage is 701 tons for endosulfan between 1994 and 2007, 1,712 tons for HCHs between 1952 and 1983, and 462 tons for DDTs between 1951 and 1983, respectively. Endosulfan usage increased dramatically in 1998 due to its application on other crops except on cotton. The HCH and DDT usage displayed a rapid increase after 1972, reaching the peak in 1976 and in 1975, respectively; since then, they declined until being banned in 1983. The gridded usage inventories of these three kinds of organochlorine pesticides in Gansu province, with a 1/4A degrees longitude by 1/6A degrees latitude resolution, have been created by using different crops for endosulfan and the area of dry farmland for HCHs and DDTs as surrogate data. The most intensive use was in northwestern regions for endosulfan and southeastern regions for HCHs and DDTs in Gansu province

Polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) in the equatorial Indian Ocean: Temporal trend, continental outflow and air-water exchange

Nineteen pairs of air and seawater samples collected from the equatorial Indian Ocean onboard the Shiyan I from 4/2011 to 5/2011 were analyzed for PCBs and HCB. Gaseous concentrations of Sigma(ICES)PCBs (ICES: International Council for the Exploration of the Seas) and HCB were lower than previous data over the study area. Air samples collected near the coast had higher levels of PCBs relative to those collected in the open ocean, which may be influenced by proximity to source regions and air mass origins. Dissolved concentrations of Sigma(ICES)PCBs and HCB were 1.4-14 pg L-1 and 0.94-13 pg L-1, with the highest concentrations in the sample collected from Strait of Malacca. Fugacity fractions suggest volatilization of PCBs and HCB from the seawater to air during the cruise, with fluxes of 0.45-34 ng m(-2) d(-1) and 0.36-18 ng m(-2) d(-1), respectively. (c) 2014 Elsevier Ltd. All rights reserved.Nineteen pairs of air and seawater samples collected from the equatorial Indian Ocean onboard the Shiyan I from 4/2011 to 5/2011 were analyzed for PCBs and HCB. Gaseous concentrations of Sigma(ICES)PCBs (ICES: International Council for the Exploration of the Seas) and HCB were lower than previous data over the study area. Air samples collected near the coast had higher levels of PCBs relative to those collected in the open ocean, which may be influenced by proximity to source regions and air mass origins. Dissolved concentrations of Sigma(ICES)PCBs and HCB were 1.4-14 pg L-1 and 0.94-13 pg L-1, with the highest concentrations in the sample collected from Strait of Malacca. Fugacity fractions suggest volatilization of PCBs and HCB from the seawater to air during the cruise, with fluxes of 0.45-34 ng m(-2) d(-1) and 0.36-18 ng m(-2) d(-1), respectively. (c) 2014 Elsevier Ltd. All rights reserved