Evaluation of fecal pollution of river sediment by detection of urobilin

In this study, we attempted to establish a new indicator for fecal pollution of river sediment using a sensitive detection method for urobilin. Urobilin contained in sediment was extracted with an alkaline buffer solution. The suitable buffer solution for extraction of urobilin consisted of 0.1 M Tris-HCl buffer (pH 10.0) containing 0.1 m sodium chloride. The ratio of sediment to buffer was 1:10. The distribution of urobilin in river sediment was studied by this method. The amount of urobilin in the river sediment of Tokyo (urban) and the Miura peninsula (rural) area was surveyed. Large quantities of urobilin were detected in the sediments of the urban rivers, but it was scarce in the rural rivers. Urobilin showed a higher content in sediment than in water. Urobilin in river sediment is distributed in large amounts in the lower reaches, where the water is polluted with domestic sewage and industrial waste, but is scarce in the upper streams. The amount of urobilin decreases to the lower layers.     

Application of Markov model to environmental fate of phenanthrene in Lanzhou Reach of Yellow River

The theory of Markov Chain is used scientifically to describe the transfer/transformation of phenanthrene in Lanzhou Reach of Yellow River. In Markov Model (MM), the states of phenanthrene in Lanzhou Reach are divided into six different states, namely being degraded, leaving the system with the addvective flow, being in air, being in water, being adsorbed on suspending substances (SS), and being in bottom sediment (BS). The MM is simulated by using Matlab6.5 to reveal the temporal changes and environmental fate of phenanthrene in Lanzhou Reach. It is shown that the environmental system will be steady in 30,000-35,000 h, the final distributions of phenanthrene in air, water, SS, and BS are 23,033 kg, 1961 kg, 800 kg, and 2824 kg respectively, with the corresponding percent of 80%, 7%, 3%, and 10%.The results of MM are approximate to the results of Fugacity Model (FM), so Markov Chain can be used to evaluate the environmental fate of pollutants in multimedia environment. The outputs of MM include the following aspects: (1) The residual time of pollutant in different environmental media and the transiting time of pollutant between different environmental media; (2) The response time of the environmental system; (3) The total mass of pollutant transferred or degraded during a given time interval; (4) The time needed for the environmental system to be steady and the final steady distributions of pollutant in the environmental system.     

Visualisation of the complexity of EUSES

The interdependencies of parameters applied in the models of EUSES are visualised in a directed connectivity graph. The parameters (inputs, defaults, state variables, outputs) are represented by boxes (nodes) and their relations by lines (edges). The visualisation, on the one hand, clarifies the complexity of the models in EUSES and, on the other hand, creates an overview and transparency. The parameters’ relations to each other can be recognised faster, and the models can be better understood. The complexity was quantified by the number (variety), kind (substance parameter, physico-chemical parameter, concentration, other parameters), and depth (dimension) of the parameter and the number of relations (connectivity). The variety of EUSES (without the modelsSimple Treat andSimple Box whose interior structure is not documented and without the effect and risk characterisation) amounts to 466, the connectivity to 961, and the maximal dimension is 21.     

An application of the theory of kinematics of mixing to the study of tropospheric dispersion

The most common technique used for numerical simulations of tracer mixing is that of the numerical solution of the advection–diffusion equation with the unresolved fluxes parameterized using the similarity theory. Despite correct predictions of the overall directions of transport, models based on a numerical solution of the advection–diffusion equation lack sufficient accuracy to correctly reproduce the coupling of mixing with small scale processes which are sensitive to the microstructure of the tracer distribution. The objective of this paper is to revisit the basic formalism employed in numerical models used to investigate atmospheric tracers. The main mathematical method proposed here is the theory of kinematics of mixing which could be applied effectively for simulations of atmospheric transport processes. At the beginning of the paper, we introduce simple mathematical transformations in order to demonstrate how complex topological structures are created by mixing processes. These idealistic flow systems are essential to explain transport properties of much more complex three-dimensional geophysical flows. An example of the application of the kinematics of mixing to the analysis of tracer transport on a planetary scale is presented in the following sections. The complex filamentary structures simulated in the numerical experiment are evaluated using some commonly applied statistical measures in order to compare the results with the data published in the literature. The results of the experiment are also analysed with the help of simple conceptual models of fluid filaments. The microstructure of the tracer distribution introduced in the paper is essential to increase our understanding of atmospheric transport and to develop more realistic parameterizations of small-scale mixing. The presented results could also be used to improve calculations of the coupling between microphysical processes and tracer mixing.     

Ca(II)在活性污泥生物絮凝中的作用研究

采用4个平行的序批式反应器(SBR),研究了进水Ca²⁺浓度对活性污泥絮体表面特性和结构稳定性的影响，并由此来确定Ca²⁺在生物絮凝中的作用。结果表明：随着进水Ca²⁺浓度的增加，污泥中的Ca含量逐渐增大。进水中Ca²⁺的加入，增大了污泥絮体的粒径和密度，进而改善了污泥的沉降性能；Ca²⁺的加入，使可供结合的蛋白质数量最高增至近1倍，污泥表面疏水性也相应增强；污泥絮凝性能的改善，主要和可供Ca²⁺结合的蛋白质含量增加有关，而非多糖；EDTA通过络合污泥絮体中的Ca²⁺，破坏了由Ca²⁺架桥形成的污泥絮体结构，这说明Ca²⁺可通过和胞外聚合物（extracellular polymeric substances, EPS）中的负电官能团架桥来促进污泥絮体的形成并维持絮体结构的稳定性。     

Nature of the field-to-field distribution of pesticide residues

The supervised trial datasets (1950), consisting of a minimum of five residue values and selected by the experts of FAO/WHO Joint Meeting on Pesticide Residues for recommending maximum residue levels between 1997 and 2011, were evaluated to obtain information on the typical spread of residue values in individual datasets. The typical relative standard deviation, CV, of field-to-field variation of pesticide residues was about 80%. The spread of residues in datasets is independent from the chemical structure of pesticides, residue level, pre-harvest interval and number of values in the datasets. The CV ranges within the Codex commodity groups and between groups overlapped and their difference were not statistically significant. The number of residues below the limit of quantification (LOQ) affects the CV at various extents depending on the ratio of LOQ/R _mean. The combined uncertainty of the highest residue in a dataset significantly affects the CV of the dataset. The lowest and intermediate ones have less influence. The residues in different fields receiving the same treatment vary within large range: 55%, 72%, 78%, 86% and 89% of the 25,766 residues values were, respectively, within 3, 4, 5, 6 and 7 times the median value of the corresponding dataset.     

Analysis of extinction in ultraviolet and visible spectra of water bodies of the Paraguay and Brazil wetlands

The extinction spectra in ultraviolet and visible radiation were analyzed using filtered and unfiltered water samples obtained in 11 open water bodies in the Neembucù (Paraguay) and Pantanal (Brazil) wetlands. The role of dissolved and suspended matter in the total extinction was analyzed between 260 nm and 700 nm. The chromophoric dissolved organic matter (CDOM) was the major component in extinction of considered ultraviolet radiation (260-400 nm). The differences in CDOM concentrations explained the main pattern of extinction of the ultraviolet radiation in the samples. Nevertheless, differences between the studied water bodies were found also to depend on the rate of photodegradation and photobleaching. The methodology developed in the present study was to distinguish "humic optic waters" according to quantity and quality of dissolved and suspended matter present. In the "humic optic water", the penetration of 10% of incident UV radiation and the photoactive layer are estimated. The influence of particulate matter increases in the total extinction of the wavelengths higher than 400 nm. The integral of the extinction curve of suspended matter in the visible wavelengths (400-700 nm) was found to relate with the total suspended solids and chlorophyll concentrations.     

杀灭菊酯对鲤鱼血液影响初探

报道了杀灭菊酯杀虫剂对鲤鱼的血液系统的影响，结果表明，（１）杀灭菊酯引起鲤鱼血浆中离子浓度发生明显改变，Ｎａ＾＋下降１０％～２０％，Ｋ＾＋下降１０％～３５％，其它离子如Ｃｌ＾－，Ｃａ＾２＋，磷等则升高；同时还观察到Ｈｂ保持不变，（２）杀灭菊酯使ＲＢＣ渗透脆性增加，在体和体外处理均能引起ＲＢＣ破损，产生溶血，这很可能是杀灭菊酯对鱼类高毒的非神经作用的重要致毒原因之一。     

Harvesting of microalgae biomass from the phycoremediation process of greywater

The wide application of microalgae in the field of wastewater treatment and bioenergy source has improved research studies in the past years. Microalgae represent a good source of biomass and bio-products which are used in different medical and industrial activities, among them the production of high-valued products and biofuels. The present review focused on greywater treatment through the application of phycoremediation technique with microalgae and presented recent advances in technologies used for harvesting the microalgae biomass. The advantages and disadvantages of each method are discussed. The microbiological aspects of production, harvesting and utilization of microalgae biomass are viewed.     

Effect of the cationic composition of sorption solution on the quantification of sorption-desorption parameters of heavy metals in soils

We obtained the sorption isotherms of Cd, Cu, Pb and Zn in clay, clay saline and organic soils. The distribution coefficients (K(d)) were determined in 0.02 eq l(-1) CaCl(2) and in a solution that simulated the soil solution cationic composition. The K(d) values greatly varied with the composition of the sorption solution and the initial metal concentration. The sorption experiments were complemented with the quantification of the extractable metal, to estimate the reversibility of metal sorption. The extraction yields depended on the metal-soil combination, and the initial metal concentration, showing no correlation with previous K(d) values. The effect of the solution composition in mobility predictions was estimated through a Retention Factor, defined as the ratio of the K(d) versus the extraction yield. Results showed that risk was over- or underestimated using the CaCl(2) medium in soils with a markedly different soil solution composition.     

Review of concentrations and chemistry of trichloroacetate in the environment

This paper reviews the concentrations of trichloroacetate (TCA) in the atmosphere-plant-soil system. Data originate mainly from Europe. The median TCA concentration in rainwater and canopy drip decreased until 1995. From then the median TCA concentration in rainwater remains rather constant while for canopy drip later data are not available. The same seems to hold for concentrations in air although a very limited data set is available. The median concentrations in coniferous needles and groundwater are constant for the period observed. The median TCA concentrations in soil decreased until 1992 and then remained constant.The TCA formation from chlorinated solvents in the atmosphere may explain a substantial percentage of the TCA amount in the atmosphere. The TCA concentrations in rainwater and canopy drip indicate that there will be other sources contributing to 10-50%. Waste incineration, biomass burning and natural formation in the marine boundary layer are potential candidate sources of TCA, but nothing can be said as yet on their TCA emission rates. Anthropogenic emissions of chlorine could also be a source.TCA can be formed from chlorinated solvents by biota. However, for coniferous trees the uptake of TCA from soil may be the predominant route. Biotic and abiotic reactions can cause to formation of TCA in soil, but also formation of TCA from chlorinated solvents by biota that excrete TCA, may contribute. Mass balance calculations of the bioactive soil top layer show that the production rate of TCA in certain soil types could be substantial. The mass balance calculations could not distinguish between natural and anthropogenic sources in soil.     

Ca(Ⅱ)在活性污泥生物絮凝中的作用研究

采用4个平行的序批式反应器(SBR),研究了进水Ca2+浓度对活性污泥絮体表而特性和结构稳定性的影响,并由此来确定Ca2+在生物絮凝中的作用.结果表明:随着进水Ca2+浓度的增加,污泥中的Ca含量逐渐增大.进水中Ca2+的加入,增大了污泥絮体的粒径和密度,进南改善了污泥的沉降性能;Ca2+的加入,使可供结合的蛋白质数量最高增至近1倍,污泥表面疏水性也相应增强;污泥絮凝性能的改善,主要和可供Ca2+结合的蛋白质含量增加有关,而非多糖;EDTA通过络合污泥絮体中的Ca2+,破坏了山Ca2+架桥形成的污泥絮体结构,这说明Ca2+可通过和胞外聚合物(extracellular polymeric substances,EPS)中的负电官能团架桥来促进污泥絮体的形成并维持絮体结构的稳定性.     

Assessment of the pollution impact on biomarkers of effect of a freshwater fish

Changes in biomarkers of fish captured from stressed environments may represent a reliable tool in revealing sublethal effects of the pollutants found in aquatic ecosystems. The response patterns of selected biochemical and morphological variables biomarkers of effect were assessed in adult females of an indigenous teleost Cnesterodon decemmaculatus, caught at a polluted site (San Francisco) of the Reconquista river (Buenos Aires, Argentina). Combined field-caging experiments with controlled laboratory exposure to clean media were performed. The biochemical parameters measured were specific activities of gill (Na+ + K+)-ATPase, liver AlaAT and AspAT, and brain AChE; LSI and CF were also calculated. The changes in gill (Na+ + K+)-ATPase and liver AlaAT activities of fish captured in the field in most cases were reversible after transfer to clean media. The results were interpreted in association with the physicochemical profile of the water samples taken simultaneously with the capture of the fish. Results suggested the suitability of the test species used as tools in environmental monitoring programs of risk assessment.     

Rates of accumulation of dieldrin by a freshwater filter feeder: Sphaerium corneum

The rate of dieldrin accumulation by Sphaerium corneum was determined in the field and under controlled conditions in the laboratory. The methods gave comparable results and it was established that Sphaerium attained an equilibrium concentration of dieldrin in its tissues in a short time period and exhibited a bioaccumulation factor of 1000. The rate of dieldrin accumulation by direct uptake from dieldrin in solution was compared to the rate obtained for indirect uptake from dieldrin adsorbed onto particulate material. The primary route of dieldrin uptake into Sphaerium was shown to be by direct partitioning of residues into lipoidal tissues from water. The effect of temperature on the rate of accumulation was also studied. The rate of accumulation increased with temperature in the range 5 degrees C to 20 degrees C. The frequency of gill cilia beat in relation to accumulation rate was studied in this temperature range and a correlation is shown.     

Influence of heavy metals on the microbial degradation of diesel fuel

The degradation of diesel fuel by a microbial community from a soil polluted by heavy metals (h.m.) in the presence of Cu, Ni, Zn, Pb, Cd, Hg and Cr (as chromate) was investigated. Experiments were conducted with soil slurries and the extracted community in liquid cultivation. The concentrations applied were in the sub-mM and mM range. Whereas the slurries displayed no significant effect, degradation in liquid culture was increasingly inhibited by higher metal concentrations. The course of degradation in suspension was demonstrated by the oxygen consumption. The order of toxicity was found to be: Hg > Cr(VI) > Cu > Cd > Ni > Pb > Zn. The absence of any effect for slurries was due to the non-availability of the metals in the soil, and to precipitation or adsorption to the soil in the case of amendment. The paper also includes results on the availability of h.m. and changes to the community after exposure.     

Kinetics and mechanisms of radiation-induced degradation of acetochlor

The radiation-induced degradation of acetochlor was investigated in this work. In a mixed solvent composed of acetonitrile and water at a ratio of 20/80 in volume, the acetochlor degradation rate was proportional to the radiation dose rate and acetochlor concentration. The acetochlor degradation efficiency was higher under alkali conditions and lower under acidic conditions. The contribution to the acetochlor degradation by the radicals was in the order of: e(aq)->.OH>H.. The quantum efficiency ratios of .OH, e(aq)- and H. for the degradation of acetochlor were calculated as 1:3:1.     

The Institute of Hydrobiology of the Chinese Academy of Sciences (1 p.)

- The Institute of Hydrobiology (IHB), Chinese Academy of Sciences (CAS) is located at the foot of Luojia Hill and beside the beautiful Donghu Lake in the City of Wuhan, Hubei Province, China. It was founded in 1930 as the Natural History Museum of Academia Sinica, and renamed as the Institute of Zoology and Botany of Academia Sinica in 1934. In 1944, it was divided into two institutes: The Institute of Zoology and Institute of Botany. In 1950, the main part of the Institute of Zoology, the sections of phycology in the Institute of Botany, and some members from other institutes and universities were merged into the Institute of Hydrobiology of the Chinese Academy of Sciences in Shanghai. The institute was moved from Shanghai to Wuhan in 1954.     

Measurement of Ambient Ground-Level Concentrations of Hydrogen Fluoride

The use of published, accepted methods for measuring ambient levels of gaseous hydrogen fluoride (HF) with a double-tape sampler led to large errors. The major source of error was found to be scrubbing In the stainless steel intake, which was avoided by substituting Teflon for the stainless steel. To avoid this and other problems encountered in the measurement of HF, we revised the double-tape sampler method and modified the double-tape sampler. We designed and constructed an HF calibrator for use in testing the revised method and modified sampler In the field and laboratory.

The results of a round robin indicated that, in the laboratory, the revised method has a single-operator precision of 3 percent at 2.6 μg/m³ and a between-laboratory precision of 4 percent. The average bias at 2.6 μg/m³ was 0.02 μg/m³ and was not significantly different from zero. Comparable precision and accuracy were obtained in the field. The response was linear, at least to 10 μg/m³. The limit of detectability, which appears to be limited by the variability in measurements of blank tapes, is 0.07 μg/m³. The revised method appears both precise and accurate.     

双硫腙法研究废电池中汞的分布及浸出

用双硫腙法测定了几种废电池中汞的含量和分布及在不同水环境条件下,汞的浸出率,试图为废电池中各组分去汞后的回收提供理论依据。结果表明,双硫腙测定废电池中汞的方法是可靠的;汞在废电池中主要分布在锌皮（锌粉）和碳包部分;pH对汞的浸出率有较大的影响,浸出率与pH呈负相关。     

Characterization of distribution of pesticide residues in crop units

The characteristic features of distribution of pesticide residues in crop units and single sample increments were studied based on more than 19,000 residue concentrations measured in root vegetables, leafy vegetables, small-, medium- and large-size fruits representing 20 different crops and 46 pesticides. Log-normal, gamma and Weibull distributions were found to provide the best fit for the relative frequency distributions of individual residue data sets. The overall best fit was provided by lognormal distribution. The relative standard deviation of residues (CV) in various crops ranged from 15–170%. The 100–120 residue values being in one data set was too small to identify potential effects of various factors such as the chemical and physical properties of pesticides and the nature of crops. Therefore, the average of CV values, obtained from individual data sets, were calculated and considered to be the best estimate for the likely variability of unit crop residues for treated field (CV = 0.8) and market samples (CV = 1.1), respectively. The larger variation of residues in market samples was attributed to the potential mixing of lots and varying proportion of non-detects. The expectable average variability of residues in composited samples can be calculated from the typical values taking into account the sample size.