Beginning in June, the input amount of water from Lake Chaohu was higher than the output amount, reaching the highest level in July and August. After September, the output amount of water was greater than the input, and the water of Lake Chaohu was gradually reduced. On the one sellekchem hand, the increase in water diluted the pollutants in the lake, and on the other hand, new pollutants were added to the lake from the area along the river. Furthermore, the use of OCPs around the lake would result in an increase in the OCP residues in spring and summer, when there are more agricultural activities. Additionally, other technical products that include HCHs or DDTs may result in this irregular seasonal variation.
Seasonal differences in the remaining pollutants were analyzed as follows: the seasonal trends of hexachlorobenzene and heptachlor, which were similar to those of HCHs, were the highest residues in winter; the residue of aldrin was at a high concentration, but the seasonal variation was inconspicuous; the pollution of isodrin and ��-chlordane was severe in summer while the concentrations of endosulfan and endrin had high values in spring. These values may have certain relationships with the application characteristics of these pollutants in general without uniform trends.Based on the spatial distribution, the sampling site JC represented the Eastern Lake and its water source areas, MS and ZM represented the Central Lake and the lakeside area of the Zhongmiao Temple, and TX represented the Western Lake region, which was near the region of the water intake.
The data in TX just included September 2010 to February 2011. To ensure the comparability among the sampling sites, the monitoring data of the other three sites were also selected from this period (Table 5). The concentration of the OCPs was 3.33ng/L from the Eastern Lake, 7.56ng/L from the Central Lake, and 6.83ng/L from the Western Lake. The pollution levels, from heavy to light, followed the order of Central Lake > Western Lake > Eastern Lake and the water source area, and the levels of OCPs in the Western and Central Lakes were more than twice those in the Eastern Lake and the water source area. The main pollutants in each region of the lake were different. The main pollutants were HCHs and DDTs in the Eastern Lake and the water source area and aldrin in the Western Lake and the Central Lake in addition to HCHs and DDTs.
Because of fewer sampling sites, the spatial differences they reflected may be influenced by the Dacomitinib environment around the sites. There was an unpopulated region near the site of JC, whereas the relatively dense residential areas were located near the sites of ZM and MS. The life or industrial emissions were also one of the factors that led to the high pollution levels of the lake.