Temporal-spatial distribution of synthetic pyrethroids in overlying water and surface sediments in Guangzhou waterways: potential input mechanisms and ecological risk to aquatic systems.

Temporal-spatial distribution of synthetic pyrethroids (SPs) in overlying water and surface sediments and ecological risk to aquatic systems were investigated, where paired water and surface sediments were collected during dry and wet periods in Guangzhou urban waterways. Eight target SPs (i.e., tefluthrin, bifenthrin, cyhalothrin, permethrin, cyfluthrin, cypermethrin, esfenvalerate, and deltamethrin), with cypermethrin and permethrin as major components, were ubiquitously detected in both water (dissolved and particle phases, separately) and sediments. Significant increases of ΣSP (sum of eight SPs) concentrations were observed in both water and sediment from the dry period to the wet period. The spatial distribution of SPs was mostly impacted by land-use type, with the highest ΣSP concentrations in the residential areas, which indicates the massive application of pyrethroids in household mosquito control. It is demonstrated that SPs preferred to be adsorbed to the particles, and rainfall-induced runoff was suggested as an important mechanism that moved SPs to the receiving waterways. A rising trend on sediment concentrations of SPs in the Guangzhou area in the last decade implied increasing application of pyrethroid insecticides, with cypermethrin and permethrin as the dominant components, where the contamination of SPs was positively related with urbanization rate (e.g., resident population and green coverage area). A special emphasis was placed on the potential effects of both individual SPs and their mixtures in three trophic levels (i.e., algae, daphnia, and fish) using toxic units (TUs) and risk quotients (RQs) for water and sediments. In spite of no acute effects due to SPs in the sediments, the toxic units showed daphnia as the most sensitive species in water, with acute risks to daphnia exhibited in several sampling sites. The risk assessment points out that a chronic toxicity (RQ index) caused by SPs in three trophic levels (algae, daphnia, and fish) exists, especially in Daphnia magna. Graphical abstract.

Profiles, sources, and transport of polycyclic aromatic hydrocarbons in soils affected by electronic waste recycling in Longtang, south China.

We studied the profiles, possible sources, and transport of polycyclic aromatic hydrocarbons (PAHs) in soils from the Longtang area, which is an electronic waste (e-waste) recycling center in south China. The sum of 16 PAH concentrations ranged from 25 to 4,300 ng/g (dry weight basis) in the following order: pond sediment sites (77 ng/g), vegetable fields (129 ng/g), paddy fields (180 ng/g), wastelands (258 ng/g), dismantling sites (678 ng/g), and former open burning sites (2,340 ng/g). Naphthalene, phenanthrene, fluoranthene, pyrene, chrysene, and benzo[b]fluoranthene were the dominant PAHs and accounted for approximately 75 % of the total PAHs. The similar composition characteristics of PAHs and the significant correlations among individual, low molecular weight, high molecular weight, and total PAHs were found in all six sampling site types, thus indicating that PAHs originated from similar sources. The results of both isomeric ratios and principal component analyses confirmed that PAHs were mainly derived from the incomplete combustion of e-waste. The former open burning sites and dismantling sites were the main sources of PAHs. Soil samples that were taken closer to the point sources had high PAH concentrations. PAHs are transported via different soil profiles, including those in agricultural fields, and have been detected not only in 0- to 40-cm-deep soil but also in 40 cm to 80 cm-deep soil. PAH concentrations in soils in Longtang have been strongly affected by primitive e-waste recycling, particularly by former open burning activities.

Characteristics, sources, and transport of tetrabromobisphenol A and bisphenol A in soils from a typical e-waste recycling area in South China.

We studied the tetrabromobisphenol A (TBBPA) and bisphenol A (BPA) patterns and their sources and transport in different land-use soils from Longtang, South China, a typical electronic waste recycling center. We also studied the reductive debromination of TBBPA in paddy soils. TBBPA and BPA concentrations (on a dry weight basis) were undetected-220 and 0.50-325 ng/g, respectively, and both increased, by similar factors, in the following order: pond sediments < paddy soils = vegetable soils < wasteland < dismantling sites < former open burning sites. BPA concentrations were higher than TBBPA concentrations in all six land-use soils, and they correlated significantly. TBBPA and BPA were transported through the soil profiles, being found at relatively high concentrations in soil 0-40 cm deep, but only at low concentrations in soil 40-80 cm deep. The surface soil concentrations appear to have been strongly affected by crude recycling activities, and former open burning and dismantling sites were the main point sources. The areas surrounding the open burning sites and dismantling sites have been contaminated not only by the dumping of waste residues but also by fly ash deposition, even though the agricultural soils are far from the point pollution sources. Some BPA in the soils is likely to be the reductive debromination product of TBBPA because the long rainy season promotes TBBPA transformation and because BPA can persist for a long time. Incubation experiments confirmed that TBBPA could be transformed into BPA and that BPA could accumulate in waterlogged paddy soils, and this may be why BPA concentrations were higher than TBBPA concentrations in the Longtang area.

Enhancement effect of two ecological earthworm species (Eisenia foetida and Amynthas robustus E. Perrier) on removal and degradation processes of soil DDT.

Effects of two ecological earthworm species (epigeic Eisenia foetida and endogeic Amynthas robustus E. Perrier) with different densities (15 and 30 individuals per kg of soil) on the removal of soil 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT) with two pollution levels (2 and 4 mg kg(-1)) were investigated. Concentrations of DDT and its metabolites, including 1,1-dichloro-2,2-bis(4-chlorophenyl)ethane (DDD), 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene (DDE), and 1-chloro-2,2-bis(4-chlorophenyl)ethylene (DDMU), were monitored after 60, 180, and 360 days of incubation. The results obtained showed that both earthworm species can significantly enhance degradation of soil DDT to its metabolites. For E. foetida, the higher earthworm density showed significantly higher rate of DDT degradation than the lower one. Anaerobic reductive dechlorination was the main degradation pathway over 180 days of incubation, while the aerobic dechlorination process was promoted between 180 and 360 days of incubation. Some earthworm amended treatments showed significantly higher microbial biomass carbon and nitrogen than the control, which suggested that earthworms might enhance the microbial degradation of DDT. Both earthworm species would have the potential to be applied to enhance the remediation of agricultural lands polluted by DDT.

Wet deposition of nitrogen and sulfur in Guangzhou, a subtropical area in South China.

With the aim of understanding the seasonal distribution of deposition fluxes of nitrogen (N) and sulfur (S) in South China, a main acid deposition region in China, precipitation samples were collected and analyzed from Guangzhou area, between March 2005 and February 2006. The estimated wet deposition of N (including ammonium nitrogen (NH(4)-N) and nitrate nitrogen (NO(3)-N)) and S (sulfate sulfur (SO(4)-S)) during the monitoring period were 40.47 kg N ha(-1) and 65.29 kg S ha(-1), respectively. The average deposition of NH(4)-N was ∼1.5 times of the NO(3)-N deposition, suggesting that the reduced and oxidized N depositions were comparable in the study area. The S and N depositions in the rainy season were greater than those in the dry season, showing great seasonal variation, which was consistent with both the distribution of precipitation and the period of fertilizer application for agriculture. The N and S wet deposition fluxes in Guangzhou were greater than those in Beijing and Zhengzhou, located in the northern China, but comparable to the level of Chongqing, located in the southwestern China, another major acid deposition region. The atmospheric N and S depositions in these cities from north to south were affected by both intensive agricultural and industrial activities.

Chemical composition and seasonal variation of acid deposition in Guangzhou, South China: comparison with precipitation in other major Chinese cities.

With the aim of understanding the origin of acid rains in South China, we analyzed rainwaters collected from Guangzhou, China, between March 2005 and February 2006. The pH of rainwater collected during the monitoring period varied from 4.22 to 5.87; acid rain represented about 94% of total precipitation during this period. The rainwater was characterized by high concentrations of SO(4)(2-), NO(3)(-), Ca(2+), and NH(4)(+). SO(4)(2-) and NO(3)(-), the main precursors of acid rain, were related to the combustion of coal and fertilizer use/traffic emissions, respectively. Ca(2+) and NH(4)(+) act as neutralizers of acid, accounting for the decoupling between high SO(4)(2-) concentrations and relatively high pH in the Guangzhou precipitation. The acid rain in Guangzhou is most pronounced during spring and summer. A comparison with acid precipitation in other Chinese cities reveals a decreasing neutralization capacity from north to south, probably related to the role and origin of alkaline bases in precipitation.