Multivariate Analysis of Interactions Between Phytoplankton Biomass and Environmental Variables in Taihu Lake, China

Phytoplankton variation in large shallow eutrophic lakes is characterized by high spatial and temporal heterogenity. Understanding the pattern of phytoplankton variation and the relationships between it and environmental variables can contribute to eutrophic lakes management. In this study Taihu Lake, one of the largest eutrophic fresh water lake in China, was taken as study area. The water body of Taihu Lake was divided into five regions viz. Wuli bay (WB), Meilian Bay (MB), West Taihu Lake (WTL), Main Body of Taihu Lake (MBTL) and East Taihu Lake (ETL). Concentrations of chlorophyll-a and the related environmental variables were determined in each region in the period 2000–2003. Factor analysis and multivariate analysis were applied to evaluate the interactions between phytoplankton variation and environmental variables. Results showed that the highest average concentrations of TN, TP and Chl-a were observed in WB, followed in a descending order by MB and WTL, and the lowest concentrations of TN, TP and Chl-a were observed in MBTL and ETL. Chl-a and TP concentrations in most regions (except ETL) declined during the study period. It suggested that to some extent the lake was recovering from eutrophication. However, persistent ascending of TN and NH₄–N in all five regions indicated the deteriorating of water quality in the study period. Results of multivariate showed that the relationships between phytoplankton biomass and environmental variables varied among regions. TP illustrated itself a controlling role on phytoplankton in WB, MB, WTL and MBTL according to the significant positive relations to phytoplankton biomass in these regions. Nitrogen could be identified as a limiting factor to phytoplankton biomass in ETL in view of the positive correlations between TN and phytoplankton and between NH₄–N and phytoplankton. Spatial variation of interactions between phytoplankton and environmental parameters suggested proper eutrophication control measures were needed to restore ecological system in each region of Taihu Lake.     

Comparative on Causes and Accumulation of Selenium in the Tree-rings Ambient High-selenium Coal Combustion Area from Yutangba, Hubei, China

Toxic trace elements emitted during coal combustion are the main sources of air pollution. They are released into the atmosphere mainly in the forms of fine ash, smoke and flue, and thus adversely affect plant, animal and human health. Selenium is one of toxic and the most volatile in coal. Large amount of atmospheric emission of selenium, as well as selenium present and scrubber stockpiles in ash may create serious environmental problems. In the paper, on the basis of investigating the abundance and distribution of selenium in plant-rings during recent 20 years, the bioaccumulation of selenium is explained that selenium in plant, which were collected from the village of selenium-rich coal combustion, is much higher than that in plants collected away from the village of selenium-rich coal combustion. The main origins of selenium are selenium-rich coal combustion and high-selenium rock weathered. The selenium recycle by food chain and selenium will accumulate and redistribute in environments.     

Polycyclic aromatic hydrocarbons in Dalian soils: distribution and toxicity assessment

Concentrations of 15 polycyclic aromatic hydrocarbons (PAHs) were measured in surface soils collected from Dalian, China, for examination of distributions and composition profiles and their potential toxicity. The sum of 15 PAHs (SigmaPAHs) ranged from 190 to 8595 ng g(-1) dry weight, and showed an apparent urban-suburban-rural gradient in both SigmaPAHs and composition profiles. Using hierarchical cluster analysis (HCA), the sampling sites were grouped into four clusters corresponding to traffic area, park/residential area, suburban and rural areas. The ratios of naphthalene (Nap) and fluorene (Fl) versus fluoranthene (Flu), pyrene (Pyr) and indeno(1,2,3-cd)pyrene (InP) in the four clusters provided evidence of local distillation. The diagnostic ratios indicated the prevalent PAH sources were petroleum combustion and coal combustion in Dalian, and a cross plot of diagnostic ratios distinguished the urban samples from suburban and rural ones. Toxic potency assessment of soil PAHs presented a good relationship with benzo(a)pyrene (BaP) levels, toxic equivalent concentrations based on BaP (TEQ(BaP)) and dioxin-like toxic equivalent concentrations (TEQ(TCDD)). The study highlights that BaP is a good indicator for assessing the potential toxicity of PAHs, and presents a promising toxicity assessment method for soil PAHs.     

Sorption of organic contaminants by biopolymers: role of polarity, structure and domain spatial arrangement

Sorption behavior of hydrophobic organic contaminants (HOCs) (i.e., pyrene, phenanthrene and naphthalene) by native and chemically modified biopolymers (lignin, chitin and cellulose) was examined. Lignins (native and treated) showed nonlinear sorption for all compounds studied, emphasizing their glassy character. Chitins and celluloses had linear isotherms for phenanthrene and naphthalene, illustrating the dominance of partitioning, while pyrene yielded nonlinear isotherms. Sorption capacity (K(oc)) of HOCs was negatively correlated with the polarity [(O+N)/C] of the biopolymers. Aromatic and alkyl+aromatic C percentages, rather than alkyl C content, demonstrated a better correlation with K(oc) values, indicating the importance of aromatic structures for HOC affinity. Hydrophobicity (K(ow))-normalized K(oc) values decreased sharply with increasing percentage of O-alkyl C versus total aliphatic C (O-alkyl C/total aliphatic C) or with polar C/(alkyl+aromatic C) ratio of the biopolymers until their values reached 80% and 4, respectively, illustrating the effect of surrounding polar groups on reducing affinity for HOCs. Overall, the results of this study highlight the role of spatial arrangement of domains within biopolymers in sorption of HOCs, and point to sorbent properties, such as functionality, polarity and structure, jointly regulating the sorption of HOCs in biopolymers.     

A biomimetic absorbent for removal of trace level persistent organic pollutants from water

A novel biomimetic absorbent containing the lipid triolein was developed for removing persistent organic pollutants (POPs) from water. The structural characteristics of the absorbent were obtained by SEM and a photoluminescence method. Under optimum preparation conditions, triolein was perfectly embedded in the cellulose acetate (CA) spheres, the absorbent was stable and no triolein leaked into the water. Dieldrin, endrin, aldrin and heptachlor epoxide were effectively removed by the CA--triolein absorbent in laboratory batch experiments. This suggests that CA-triolein absorbent may serve as a good absorbent for those selected POPs. Triolein in the absorbent significantly increased the absorption capacity, and lower residual concentrations of POPs were achieved when compared to the use of cellulose acetate absorbent. The absorption rate for lipophilic pollutants was very fast and exhibited some relationship with the octanol--water partition coefficient of the analyte. The absorption mechanism is discussed in detail.     

Generalized models for prediction of pentachlorophenol dissipation dynamics in soils

Dissipation of pentachlorophenol (PCP) in soil was investigated and the chemical relationships with soil properties were addressed. The results indicate that the dissipation of extractable PCP residues can be described using first-order kinetics equations, with a half-dissipation time (T(1/2)) ranging from 6.5 to 173.3d. The sharply different patterns of PCP dissipation in different soils were closely related to soil properties. Correlations of stepwise regression equations obtained were significant at 0.01 probability level between soil parameters and extractable PCP residues (R(2)=0.974**) as well as T(1/2) values (R(2)=0.882**). Using pH together with organic carbon content (OC) and soil particle size distribution, the dissipation dynamics of PCP in soil could be accurately predicted.     

Analysis of patterns and ecological security trend of modern oasis landscapes in Xinjiang, China

Ecological security has become so important that it will affect the national security and social sustainable development. In this paper, a case study on the ecological security indexes of modern oasis landscapes in Beitun Oasis, Xinjiang, was carried out. The spatial neighbouring parameters, such as the contiguous length, measure of area and patch quantity of oasis landscape patches, affected by desert landscape patches were calculated by using GIS-based buffer analysis, the method of calculating ecological security indexes of oasis landscape was developed, and the dynamic changes of patterns and ecological security indexes of the oasis landscapes since recent 30 years were analyzed. The results showed that soil salinization or alkalization and paludification were major factors affecting the ecological security in Beitun Oasis. Therefore, measures should be taken actively to prevent and control secondary salinization and paludification. The ecological security indexes of the oasis landscape in 1972, 1990 and 2005 were 78.91, 82.28 and 83.86, respectively, which showed the degree of security is improving, and the environment was developing harmoniously between human and nature. The methods of evaluating ecological security based on the spatial neighbouring relations between landscape patches can be used to reflect preliminarily the ecological security patterns of landscapes.     

Catalytic activity of Ru/Al2O3 for ozonation of dimethyl phthalate in aqueous solution

With dimethyl phthalate as the model pollutant and Ru/Al(2)O(3) as catalyst, this paper systemically investigates the removal of total organic carbon (TOC) of system. Our results have confirmed that Ru/Al(2)O(3) can significantly increase the effect of ozonation. TOC removal in 120 min can reach 72% while only 24% with ozone alone. The optimal catalyst preparing condition was 0.1 wt% Ru content, 600 degrees C calcination temperature, 0.5-1.0mm particle diameter, which is characterized by a high surface area and a large population of surface active sites. The contrasting experiments of ozone alone, catalyst adsorption after ozonation, and catalytic ozonation confirmed that catalytic reaction was the most important process to TOC removal in system with Ru/Al(2)O(3) as catalyst.