Yu-Jiao Jiang

Spatio-temporal distributions and the ecological and health risks of phthalate esters (PAEs) in the surface water of a large, shallow Chinese lake.

The spatio-temporal distributions and the ecological and health risks of PAEs in surface water of Lake Chaohu, the fifth largest lake in China, were studied based on the monthly monitoring of six PAE congeners from May 2010 to April 2011. The annual total concentration of the six PAE congeners (Σ6PAE) in the surface water ranged from 0.467 to 17.953 μg L(-1), with the average value of 4.042±3.929 μg L(-1). The di-n-butyl phthalate (DnBP) that dominated the Σ6PAE at 65.8% was found at its highest and lowest levels in the western lake (TX) and eastern drinking water source area (JC), respectively. The temporal distributions of Σ6PAE showed that the highest and lowest levels were observed in September 2010 and June 2010, respectively. The different relationships between the runoff and the PAEs with low and high levels of carbon might suggest their different sources. The DnBP had much greater ecological risks than the other studied PAE congeners as indicated by its potential affected fractions (PAFs) and the margin of safety (MOS10). The PAE congeners studied posed little health risk to the nearby male and female citizens.

Distribution, partitioning and sources of polycyclic aromatic hydrocarbons in the water-SPM-sediment system of Lake Chaohu, China.

The residual levels of polycyclic aromatic hydrocarbons (PAHs) in the water, suspended particular matter (SPM) and sediment from Lake Chaohu were measured with a gas chromatograph-mass spectrometer (GC-MS). The spatial-temporal distributions and the SPM-water partition of PAHs and their influencing factors were investigated. The potential sources and contributions of PAHs in the sediment were estimated by positive matrix factorization (PMF) and probabilistic stable isotopic analysis (PSIA). The results showed that the average residual levels of total PAHs (PAH16) in the water, SPM and sediment were 170.7 ± 70.8 ng/L, 210.7 ± 160.7 ng/L and 908.5 ± 1878.1 ng/g dry weight, respectively. The same spatial distribution trend of PAH16 in the water, SPM and sediment was found from high to low: river inflows>western lake>eastern lake>water source area. There was an obvious seasonal trend of PAH16 in the water, while no obvious seasonal trend was found in the SPM. The residues and distributions of PAHs in the water, SPM and sediment relied heavily on carbon content. Significant Pearson correlations were found between LogKoc and LogKow as well as some hydro-meteorological factors. Three major sources of PAHs including coal and biomass combustions, and vehicle emissions were identified.

Residues, Distributions, Sources, and Ecological Risks of OCPs in the Water from Lake Chaohu, China

The levels of 18 organochlorine pesticides (OCPs) in the water from Lake Chaohu were measured by a solid phase extraction-gas chromatography-mass spectrometer detector. The spatial and temporal distribution, possible sources, and potential ecological risks of the OCPs were analyzed. The annual mean concentration for the OCPs in Lake Chaohu was 6.99 ng/L. Aldrin, HCHs, and DDTs accounted for large proportions of the OCPs. The spatial pollution followed the order of Central Lakes > Western Lakes > Eastern Lakes and water area. The sources of the HCHs were mainly from the historical usage of lindane. DDTs were degraded under aerobic conditions, and the main sources were from the use of technical DDTs. The ecological risks of 5 OCPs were assessed by the species sensitivity distribution (SSD) method in the order of heptachlor > γ-HCH > p,p′-DDT > aldrin > endrin. The combining risks of all sampling sites were MS > JC > ZM > TX, and those of different species were crustaceans > fish > insects and spiders. Overall, the ecological risks of OCP contaminants on aquatic animals were very low.

Polybrominated diphenyl ethers (PBDEs) in the surface sediments and suspended particulate matter (SPM) from Lake Chaohu, a large shallow Chinese lake

Suspended particulate matter (SPM) and surface sediment samples were collected from Lake Chaohu to investigate the residues, congener profile, and spatial distribution of polybrominated diphenyl ethers (PBDEs) in a large shadow lake in the middle of the Yangtze River Basin. The concentration of Σ13BDEs (defined as the sum of 13 target congeners excluding BDE 209) and the concentration of BDE 209 ranged from 236.7 to 1373.4 pg/g dry weight (dw) and from 4.2 to 691.2 pg/g dw in the surface sediments, respectively, which were 2-3 orders of magnitude smaller than those found in the SPM. The congener composition was dominated by BDE 47 (50.8%) and BDE 209 (21.3%) in the sediment, while the proportion of BDE 47 to Σ14BDEs in the SPM was slightly higher than that in the sediment. The concentration of Σ14BDEs in the sediment from the drinking water source (WR) area in the eastern part of the lake was very low, with a mean value of 514.8 pg/g, whereas the mean concentration was 102.4 ng/g in the SPM. A cluster analysis (CA) was conducted to further illustrate the dominance of each congener and the similarity of each sampling site. Many factors, including resuspension, photodecomposition, microbial oxidation, local discharge, and dredging, influenced the distribution in the sediment and SPM for the PBDE congeners as well as the spatial distribution of PBDEs. A formula for the PBDE concentrations in the surface sediment and SPM was constructed to understand the potential relationship between sediment and SPM concentrations. Although the formula did not accurately predict specific PBDE congener concentrations in the sediment, it remains a practical and useful way to assess the overall pollution of PBDE in sediment in Lake Chaohu, as it depends only on the concentrations of PBDEs in the SPM.

Levels, Temporal-Spatial Variations, and Sources of Organochlorine Pesticides in Ambient Air of Lake Chaohu, China

The residual levels of OCPs in the gas phase and particle phase in Lake Chaohu, China, were measured using GC-MS from March 2010 to February 2011. The temporal-spatial variations and sources of OCPs were also analyzed. Twenty types of OCPs were detected in the gas phase with a total concentration of 484.8 ± 550.4 pg/m3. Endosulfan, DDTs and chlordane were the primary OCPs in the gas phase. The mean concentration of OCPs in the gas phase was significantly higher in the summer than in the winter. Seventeen types of OCPs were detected in the particle phase with a total concentration of 18.3 ± 26.1 pg/m3. DDTs were major OCPs in the particle phase. The mean concentration of OCPs in the particle phase decreased at first and then increased during the period. The potential source of the HCHs in ambient air of Lake Chaohu might come from recent lindane usage. DDTs mainly came from historical dicofol usage, and an input of DDT was observed in the spring, which may result from the present use of marine paint that contains technical DDT. Endosulfan and chlordane in the air may be due to the present use of technical endosulfan and chlordane.

Simulation of the fate and seasonal variations of α-hexachlorocyclohexane in Lake Chaohu using a dynamic fugacity model.

Fate and seasonal variations of α-hexachlorocyclohexane (α-HCH) were simulated using a dynamic fugacity model in Lake Chaohu, China. Sensitivity analyses were performed to identify influential parameters and Monte Carlo simulation was conducted to assess model uncertainty. The calculated and measured values of the model were in good agreement except for suspended solids, which might be due to disregarding the plankton in water. The major source of α-HCH was an input from atmospheric advection, while the major environmental outputs were atmospheric advection and sediment degradation. The net annual input and output of α-HCH were approximately 0.294 t and 0.412 t, respectively. Sediment was an important sink for α-HCH. Seasonal patterns in various media were successfully modeled and factors leading to this seasonality were discussed. Sensitivity analysis found that parameters of source and degradation were more important than the other parameters. The sediment was influenced more by various parameters than air and water were. Temperature variation had a greater impact on the dynamics of the model output than other dynamic parameters. Uncertainty analysis showed that the model uncertainty was relatively low but significantly increased in the second half of the simulation period due to the increase in the gas-water diffusion flux variability.

Toxic Effects of Ethyl Cinnamate on the Photosynthesis and Physiological Characteristics of Chlorella vulgaris Based on Chlorophyll Fluorescence and Flow Cytometry Analysis

The toxic effects of ethyl cinnamate on the photosynthetic and physiological characteristics of Chlorella vulgaris were studied based on chlorophyll fluorescence and flow cytometry analysis. Parameters, including biomass, F v/F m (maximal photochemical efficiency of PSII), ФPSII (actual photochemical efficiency of PSII in the light), FDA, and PI staining fluorescence, were measured. The results showed the following: (1) The inhibition on biomass increased as the exposure concentration increased. 1 mg/L ethyl cinnamate was sufficient to reduce the total biomass of C. vulgaris. The 48-h and 72-h EC50 values were 2.07 mg/L (1.94–2.20) and 1.89 mg/L (1.82–1.97). (2) After 24 h of exposure to 2–4 mg/L ethyl cinnamate, the photosynthesis of C. vulgaris almost ceased, manifesting in ФPSII being close to zero. After 72 h of exposure to 4 mg/L ethyl cinnamate, the F v/F m of C. vulgaris dropped to zero. (3) Ethyl cinnamate also affected the cellular physiology of C. vulgaris, but these effects resulted in the inhibition of cell yield rather than cell death. Exposure to ethyl cinnamate resulted in decreased esterase activities in C. vulgaris, increased average cell size, and altered intensities of chlorophyll a fluorescence. Overall, esterase activity was the most sensitive variable.