Biomonitoring of bisphenol A, 4-nonylphenol,and 4-t-octylphenol in Turkish population: exposure and risk assessment

Environmental Science and Pollution Research - Biomonitoring studies are important tools to understand the effects of endocrine-disrupting compounds on human health. Up to now, there have been no...     

Analysis of 4-nonylphenols, phthalates, and polychlorinated biphenyls in soils and biosolids

When sewage sludge is added to agricultural land, organic chemicals contaminants are also added. The fate of these chemicals, particularly those shown to have oestrogenic potential, has received much research and regulatory interest in recent years. A method was developed for the analysis of 4-nonylphenols, phthalates, and PCB congeners in soils, mesophilic anaerobially digested dewatered (MADD) sewage sludge, and MADD sludge-amended soil. After Soxhlet-extraction, the 4-nonylphenols and phthalates were separated from the PCBs on an isolute cyanopropyl SPE cartridge and analysed by GC-MS directly. The PCBs were acid treated on a Bakerbond PCB-A cartridge, then passed through a gel filtration column of Biobeads SX-3 resin, before GC-MS analysis. The method was successfully validated and then used for routine analysis, where average recoveries of the surrogate standards were 83+/-17% (4-n-heptylphenol), 96+/-11% (dimethyl-tere-phthalate), 101+/-12% (dibenzyl-phthalate), and 79+/-13% (PCBs 6, 54, 104, 155, and 198).     

Field dissipation of 4-nonylphenol, 4-t-octylphenol, triclosan and bisphenol A following land application of biosolids

The persistence of contaminants entering the environment through land application of biosolids needs to be understood to assess the potential risks associated. This study used two biosolids treatments to examine the dissipation of four organic compounds: 4-nonylphenol, 4-t-octylphenol, bisphenol A and triclosan, under field conditions in South Australia. The pattern of dissipation was assessed to determine if a first-order or a biphasic model better described the data. The field dissipation data was compared to previously obtained laboratory degradation data. The concentrations of 4-nonylphenol, 4-t-octylphenol and bisphenol A decreased during the field study, whereas the concentration of triclosan showed no marked decrease. The time taken for 50% of the initial concentration of the compounds in the two biosolids to dissipate (DT50), based on a first-order model, was 257 and 248 d for 4-nonylphenol, 231 and 75 d for 4-t-octylphenol and 289 and 43 d for bisphenol A. These field DT50 values were 10- to 20-times longer for 4-nonylphenol and 4-t-octylphenol and 2.5-times longer for bisphenol A than DT50 values determined in the laboratory. A DT50 value could not be determined for triclosan as this compound showed no marked decrease in concentration. The biphasic model provided a significantly improved fit to the 4-t-octylphenol data in both biosolids treatments, however, for 4-nonylphenol and bisphenol A it only improved the fit for one treatment. This study shows that the use of laboratory experiments to predict field persistence of compounds in biosolids amended soils may greatly overestimate degradation rates and inaccurately predict patterns of dissipation.     

4th International Clean Air Congress May 16 ∼ 20, 1977 Tokyo

The ways in which anhydrous ammonia may accidentally escape to the atmosphere from refrigerated or pressurized containment are systematically reviewed. The circumstances in which the ammonia may form part of a mixture which is buoyant, neutrally buoyant, or denser than air are described and for each mode of release there is a discussion of the likely density of the resulting ammonia cloud.     

TiO2纳米管催化降解4，4’-二溴联苯的影响因素和动力学研究

利用TiO2纳米管催化降解水中的4，4’-二溴联苯，对催化降解过程和影响因素进行研究。结果表明，TiO2纳米管对其有较高的催化降解效率且降解过程符合Langmuir—Hinshelwood动力学模式。不同光源、4，4’-二溴联苯的初始浓度、纳米管添加量和pH值对催化降解过程都有较大影响，其中pH值的影响最为明显。反应液在中性状态下的降解率明显低于pH=1或11的情况。在pH=1时，4，4’一二溴联苯的降解率达86％。     

Reconstruction of the pollution history of alkylphenols (4-tert-octylphenol, 4-nonylphenol) in the Baltic Sea

This paper reports the reconstruction of the pollution history of 4-tert-octylphenol (OP) and 4-nonylphenol (NP) in the Baltic Sea. Alkylphenols are endocrine-disrupting compound and therefore toxic to aquatic organisms. Sediment cores were collected from regions with relatively stable sedimentation conditions. The cores were dated by the ²¹⁰Pb method. The OP and NP were determined using HPLC-FL. The highest inventory of these compounds was observed in the Gotland Deep (610 μg m² of NP and 47 μg m² of OP) and the lowest—on the slope of the Gdansk Deep (24 μg m² of NP and 16 μg m² of OP). Such spatial distribution was probably, among other factors, the result of the uplift of the sea floor. The pollution trends of OP and NP in sediments coincided with the following: (1) the beginnings of eutrophication (1960s/1970s of the twentieth century) and (2) strong increase in the areal extent and volume of hypoxia and anoxia in the Baltic (present century).     

Comparative effects of oral exposure to 2, 4, 6-tribromophenol and decabromodiphenyl ether in Nile tilapia

Environmental Science and Pollution Research - Flame retardants are compounds added to a high diversity of polymers used in electronics and furniture to decrease the risk of combustion....     

Effects of fulvic acid on aggregation,sedimentation, and adsorption of Fe3O4 magnetic nanoparticles

Environmental Science and Pollution Research - Environmental behavior, bioavailability, and risks posed by Fe3O4, magnetic nanoparticles (Fe3O4 NPs) in surface waters are affected by complex...     

TiO2膜光催化降解4，4’-二溴联苯的研究

研究了负载于玻璃上的固定化催化剂TiO2膜光催化降解水中4，4’-二溴联苯（4，4’-DBB）的效果，考察了溶液pH值和4，4’-DBB初始浓度等对TiO2膜光催化降解4，4’-DBB的影响，探讨了降解机理。结果表明，TiO2膜光催化降解水中4，4’-DBB的效果良好，紫外光照射8h，初始浓度为4mg／L的4，4’-DBB的降解率高达94％，降解速率随着4，4’-DBB初始浓度的增大而下降。在溶液pH：1时，4，4’-DBB的降解效率最高。超声的加入使降解反应的速率加快。经拟合发现4，4’-DBB的降解符合拟一级反应规律，并推导出动力学方程。     

Influence of preparation method on structural,optical, magnetic,and adsorption properties of nano-NiFe2O4

Nickel ferrite (NiFe₂O₄) nanoparticles are prepared through different routes (microwave, co-precipitation, and pyrolysis) and tested for water purification applications through adsorption removal of an acid red dye B as a model organic pollutant. The characterizations of the prepared samples were done using XRD, FT-IR, SEM, TEM, BET, UV-Vis absorbance, Raman spectrum, and vibrating sample magnetometer (VSM). All samples showed an inverse spinel crystal structure. The obtained results pointed out to the effect of the synthetic route on the morphology, particle size, optical, and magnetic properties of the prepared ferrites. Magnetic measurements showed super-paramagnetic behavior for all samples. The magnetic saturation (M_s) of the sample prepared by pyrolysis, was found to possess the highest saturation value, 34.8 emu/g. Adsorption experiments were performed under the change in several parameters, such as pH, adsorbent dosage, and initial dye concentration. A dye removal percentage of 99% was reached under the optimum state. The isothermal adsorption of the acid red dye was investigated using several models, in which the experimental data could be best described by the Freundlich model. Several kinetic and equilibrium models were inspected by linear regression analysis and showed best fitting for the adsorption data through pseudo-second-order model. The calculated thermodynamic parameters indicated that the adsorption of acid red dye onto all the ferrite samples is a spontaneous and endothermic physical adsorption process.

     

Revised relative potency values for PCDDs, PCDFs, and non-ortho-substituted PCBs for the optimized H4IIE-luc in vitro bioassay

While the World Health Organization 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) equivalency factors are useful estimates of relative potencies of mixtures when conducting risk assessments, they are not useful when comparing the results of bioassays such as the H4IIE-luc to concentrations of TCDD equivalents calculated from instrumental analyses. Since there are thousands of dioxin-like compounds (DLCs), one use of screening assays is to determine if all of the aryl hydrocarbon receptor (AhR) active DLCs in a mixture have been accounted for in instrumental analyses. For this purpose, bioassay-specific relative potency (ReP) values are needed. RePs of 21 polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans, and dioxin-like polychlorinated biphenyls that exhibit effects mediated through the AhR were determined by use of the H4IIE-luc assay. Different values of RePs are derived, depending on the statistical, curve-fitting methods used to derive them from the dose–response relationships. Here, we discuss the various methods for deriving RePs from in vitro data and their assumptions and effects on values of RePs. Full dose–response curves of 2,3,7,8-TCDD and other representative DLCs were used to estimate effective concentrations at multiple points (e.g., EC20-50-80), which were then used to estimate ReP of each DLC to 2,3,7,8-TCDD.     

Absorption, balance and metabolism of C-2, 4, 6-trichlorophenol in hydroponic tomato plants

Most of the 2, 4, 6-TCP applied in the nutrient solution of the hydroculture test was volatilised; a proportion was absorbed by the developed plant roots and to a small extent isomerised. Significant portions of the non-extractable tomato plant residues were found in the isolated lignin and cellulose fractions.     

An Air Quality Data Analysis System for Interrelating Effects,Standards, and Needed Source Reductions: Part 4. A Three-Parameter Averaging-Time Model

Urban air pollutant concentration data often tend to fit a two-parameter averaging-time model having three characteristics: (1) pollutant concentrations are (two-parameter) lognormally distributed for all averaging times; (2) median concentrations are proportional to averaging time raised to an exponent; and (3) maximum concentrations are approximately inversely proportional to averaging time raised to an exponent. Concentration data obtained near many isolated point sources and in some urban areas often do not fit a two-parameter lognormal distribution. An increment (either positive or negative) can be added to each such concentration in order to fit the data instead to a three-parameter lognormal distribution. This increment has been incorporated as the third parameter in a new three-parameter averaging-time model that can be used in both point-source and urban settings. Examples show how this new model can be used to analyze SO₂ concentration data obtained near a point source to determine the degree of emission reduction needed to achieve the national ambient air quality standards.     

Comparison of manual and automated chambers for field measurements of N2O,CH4, CO2 fluxes from cultivated land

Chamber techniques can easily be applied to field trials with multiple small plots measuring carbon- and nitrogen-trace gas fluxes. Nevertheless, such chamber measurements are usually made weekly and rarely more frequently than once daily. However, automatic chambers do allow flux measurements on sub-daily time scales. It has been hypothesized that sub-daily measurements provide more reliable results, as diurnal variations are captured better compared to manual measurements. To test this hypothesis we compared automatic and manual measurements of N₂O, CO₂ and CH₄ fluxes from tilled and non-tilled plots of a rice–wheat rotation ecosystem over a non-waterlogged period. Our results suggest that both techniques, i.e., either manual or automatic chambers of N₂O and CO₂ emissions resulted in biased fluxes. The manual measurements were adequate to capture either day-to-day or seasonal dynamics of N₂O, CO₂ and CH₄ exchanges, but overestimated the cumulative N₂O and CO₂ emissions by 18% and 31%, respectively. This was due to neglecting temperature-dependent diurnal variations of C and N trace gas fluxes. However, the automatic measurements underestimated the cumulative emissions of N₂O and CO₂ by 22% and 17%, respectively. This underestimation resulted from chamber effects upon soil moisture during rainfall processes. No significant difference was detected between the two methods in CH₄ exchanges over the non-waterlogged soils. The bias of manual chambers may be significant when pronounced diurnal variations occur. The bias of automatic measurements can only be avoided/minimized if chamber positions are frequently changed and/or if chambers are automatically opened during rainfall events. We therefore recommend using automatic chambers together with continuous measurements of soil chamber moisture to allow for soil moisture correction of fluxes or to correct flux estimates as derived by manual chambers for possible diurnal variations.     

BRC4Env,a network of Biological Resource Centres for research in environmental and agricultural sciences

The Biological Resource Centre for the Environment BRC4Env is a network of Biological Resource Centres (BRCs) and collections whose leading objectives are to improve the visibility of genetic and biological resources maintained by its BRCs and collections and to facilitate their use by a large research community, from agriculture research to life sciences and environmental sciences. Its added value relies on sharing skills, harmonizing practices, triggering projects in comparative biology, and ultimately proposing a single-entry portal to facilitate access to documented samples, taking into account the partnership policies of research institutions as well as the legal frame which varies with the biological nature of resources. BRC4Env currently includes three BRCs: the Centre for Soil Genetic Resources of the platform GenoSol, in partnership with the European Conservatory of Soil Samples; the Egg Parasitoids Collection (EP-Coll); and the collection of ichthyological samples, Colisa. BRC4Env is also associated to several biological collections: microbial consortia (entomopathogenic bacteria, freshwater microalgae…), terrestrial arthropods, nematodes (plant parasitic, entomopathogenic, animal parasitic...), and small mammals. The BRCs and collections of BRC4Env are involved in partnership with academic scientists, as well as private companies, in the fields of medicinal mining, biocontrol, sustainable agriculture, and additional sectors. Moreover, the staff of the BRCs is involved in many training courses for students from French licence degree to Ph.D, engineers, as well as ongoing training.     

Juvenile sea bass biotransformation, genotoxic and endocrine responses to beta-naphthoflavone, 4-nonylphenol and 17 beta-estradiol individual and combined exposures

Juvenile sea bass, Dicentrarchus labrax L., were exposed during 2, 4, 8, and 24 h to 0.9 microM beta-naphthoflavone (BNF), 131 nM 17 beta-estradiol (E(2)), 4.05 microM 4-nonylphenol (NP), as well as to BNF combined either to E(2) or NP (maintaining the previous concentrations). Liver cytochrome P450 content (P450), ethoxyresorufin-O-deethylase (EROD), and glutathione S-transferase (GST) activities were measured in order to evaluate biotransformation responses. Genotoxicity was assessed as erythrocytic nuclear abnormalities (ENA) frequency. The effects on endocrine function were evaluated as plasma cortisol and glucose. Cortisol was not affected by xeno/estrogens tested, either in single exposure or mixed with BNF. Nevertheless, the intermediary metabolism was affected since glucose concentration increased after 4 h exposure to E(2), and after all BNF+NP exposure lengths. Moreover, a synergism between BNF and NP was thoroughly demonstrated, whereas a sporadic antagonistic interaction was found at 4 h BNF + E(2) exposure. Liver EROD and GST activities were not significantly altered by single E(2) or NP exposure. However, both compounds were able to induce EROD activity in the presence of BNF. NP single exposure was able to significantly increase liver P450 content, while its mixture with BNF displayed an antagonistic interference. Considering the xeno/estrogens single exposures, only NP induced an ENA increase; however, both mixtures (BNF + E(2) and BNF + NP) displayed genotoxic effects. Fish responses to mixtures of xenobiotics are complex and the type of interaction (synergism/potentiation or antagonism) in a particular mixture can vary with the evaluated biological response.