Disposition of bisphenol A in pregnant mice and fetuses after a single and repeated oral administration

The risk assessment of bisphenol A (BPA) on the development of offspring of humans is an important issue. There have been some reports on the fate of BPA in rodents, but information on the BPA level in fetal organs essential for the extrapolation to humans is inadequate. In the present study, we investigated the distribution pattern of ¹⁴C-BPA-derived radioactivity in fetal tissues following administration of 10?mg/kg ¹⁴C-BPA to the pregnant mice. The radioactivity was rapidly transferred through placenta and distributed to all fetal organs including reproductive organs and brains in a similar level. The concentration declined slowly compared with dams. Analysis of metabolites in fetuses showed that a fraction of BPA was unexpectedly large compared to the maternal blood. There was no clear effect of the fetal position in a uterus to influence the radioactivity concentration in whole fetuses. The dose dependence of pharmacokinetics should be recognized to extrapolate the pharmacokinetic result from animal experiments at high doses to humans at low doses. Similar experiments were conducted with an addition of two doses, 1 and 100?mg/kg, respectively. The pharmacokinetics seemed to be linear between 1 and 10?mg/kg, although at 100?mg/kg BPA was absorbed slowly and the radioactivity concentrations in fetuses were much higher than expected based on the linear dose dependence. Repeated doses were administered to pregnant mice since humans are exposed to BPA chronically. Radioactivity level in most of the fetal tissues on repeated administration was higher than single administration.     

Optimizing nutrient supply in a rotatory-switching biofilter for toluene vapor treatment

The influence of nutrient conditions on the degradation of toluene vapor in a rotatory-switching biofilter (RSB) was investigated. The biofilter consists of four segments connected in series, each with a packing layer made of polyvinyl formal. The influent airstreams including toluene vapors were passed through segments 1-3 as up-flow with a toluene concentration of 0.9-1.2 g m(-3) and with an empty-bed retention time of 26-52 sec. Nutrient solutions were fed to all packed segments once a day by means of immersion. The nutrient solution was used repeatedly and replenished by the addition of (NH4)2SO4. The result at 155 days showed nitrogen depletion was particularly obvious and the lack of nitrogen affected toluene removal. By adding 161 g of nitrogen solution per volumetric cubic meter of reactor, toluene removal efficiency was immediately increased to greater than 99%. With long-term biofilter operation, 21%-32% of ammonium was utilized for nitrification because of the growth of nitrifying bacteria such as Nitrosomonas sp. Based on the carbon-nitrogen balance, the daily nitrogen demand for toluene removal was estimated 2.1 g day(-1) at a toluene load of 70 g m(-3) hr(-1).     

A GIS-based zoning of illegal dumping potential for efficient surveillance

To assist in the efficient surveillance against illegal dumping, this study examined and evaluated two methods to illustrate the illegal dumping potential of sites using GIS (Geographic Information System) data. One approach focused on the occurrence of illegal dumping sites; the other on the size of the illegal dumping. Both approaches to zoning were implemented for the Kanto region of Japan, utilizing seven or eight major geographical attributes most closely related to illegal dumping. The zoning results revealed the areas requiring patrols against illegal dumping. Evaluation of the zoning results using the ROC (Receiver Operating Characteristic) curve showed the number of illegal dumping sites detectable under certain surveillance conditions and that the size-based zoning was superior, but this superiority was insignificant for revealing sites with higher potential for large illegal dumping, for which it would be sufficient to use the occurrence-based zoning. The evaluation also showed the contribution of each geographical attribute. Finally, application of the ROC curve to the surveillance planning process was examined, which enables the total social cost of pollution by illegal dumping, rehabilitation of dumping sites, and illegal dumping surveillance to be minimized.     

Temporal moments analysis of preferential solute transport in soils

Temporal moments analysis of solute breakthrough curves is used to investigate the preferential leaching of chloride, nitrate and phosphate through an Australian soil. Recent studies have shown that current models and methods do not adequately describe the leaching of nutrients through soil, often underestimating the risk of groundwater contamination by surface-applied chemicals, and overestimating the concentration of resident solutes. This inaccuracy results primarily from ignoring soil structure and non-equilibrium between soil constituents, water and solutes. Therefore simple models are required to accurately characterise solute transport in natural and agricultural soils under non-equilibrium conditions. A multiple sample percolation system, consisting of 25 individual collection wells was constructed to study the effects of localised soil heterogeneities on the transport of nutrients (NO₃ ^–, Cl^–, PO₄ ^{3 –}) in the vadose zone of an agricultural soil predominantly dominated by clay. Using data collected from the multiple sample percolation experiments, this paper compares and contrasts the performance of temporal moments analysis with two mathematical models for predicting solute transport, the advective-dispersion model with a reaction term (ADR) and a two-region preferential flow model (TRM) suitable for modelling preferential transport. The values for solute transport parameters predicted by temporal moments analysis were in excellent agreement with experimental data and results from ADR and TRM. It is concluded that temporal moments analysis when applied with other physical models such as the ADR and TRM, provide an excellent means of obtaining values for important solute transport parameters and gaining insight of preferential flow. These results have significant ramifications for modelling solute transport and predicting nutrient loadings.     

Seasonal changes in microbial heterotrophic activity in subarctic marine waters as related to phytoplankton primary productivity

Water samples were collected in and near Kasitsna Bay (Cook Inlet), Alaska over 18 mo (February 1979–August 1980). Seasonal changes in glucose and glutamate uptake rates were measured in these samples. During the second year of the study, the uptake rates of glycolate and acetate and primary productivity were also measured. Of the substrates tested, significant positive linear correlations were observed between glucose and glutamate uptake and primary productivity. A higher correlation was observed between glucose to glutamate uptake ratios and primary productivity. The seasonal patterns of glucose uptake, glucose-to-glutamate uptake ratios and primary productivity rates show that the ratios changes simultaneously with fluctuations in primary productivity rates. The glucose uptake patterns reveal a delay in the response of the glucose-utilizing microorganisms to the onset of the bloom. It is suggested that by measuring the uptake rates of the simple compounds by microheterotrophs, and comparing these rates with each other, one can determine the relative flux of these compounds through the system. If the major source of these compounds is material released into the seawater by phytoplankton, it is possible that this approach could characterize the flux of extracellular products. As more is known about how the composition of extracellular material relates to the physiological state of phytoplankton, such an approach may eventually be a useful indirect assessment of the physiological state of natural phytoplankton populations.Published as Technical Paper No. 6397, Oregon Agricultural Experiment Station     

Horizontal distribution of steroid estrogens in surface sediments in Tokyo Bay

A monitoring survey was conducted to investigate the distribution of steroid estrogens and their conjugates in surface sediments of Tokyo Bay for the first time, which is known as one of the most heavily polluted marine embayments in the world. The surface sediment samples were collected at 20 locations covering the whole area of Tokyo Bay and analyzed for steroid estrogens and their conjugates using liquid chromatography-tandem mass spectrometry. The concentrations of 17beta-estradiol (beta-E2) and estrone (E1) ranged from ND (below the detection limit; <0.07) to 0.59 and from 0.05 to 3.60 ng g-1 dry, respectively. Those concentrations were higher in the northern part of the bay, which is directly receiving huge quantities of pollutants from adjacent rivers containing a large amount of municipal and industrial wastewater. 17alpha-Estradiol (alpha-E2) and estrone-3-sulfate (E1-3S) were detected in some of the samples, whereas neither of the other conjugates, estriol (E3) or 17alpha-ethynylestradiol (EE2), was found.     

Investigation of nuclear enzyme topoisomerase as a putative molecular target of monohaloacetonitrile disinfection by-products

Disinfection by-products occur widely as the unintended effect of water disinfection and are associated with toxicity and adverse human health effects. Yet the molecular mechanisms of their toxicity are not well understood. To investigate the molecular basis of hyperploidy induction by monohaloacetonitriles, the interaction of monohaloacetonitriles with topoisomerase Ⅱ in Chinese hamster ovary cells was examined. We showed a concentration-dependent inhibition of DNA decatenation activity of topoisomerase under acellular conditions while in vitro monohaloacetonitrile treatment expressed mixed results. The working hypothesis, that topoisomerase Ⅱ is a molecular target of monohaloacetonitriles, was only partially supported.Nevertheless, this research serves as a starting point toward molecular mechanisms of toxic action of monohaloacetonitriles.     

Detoxification of hexachlorobenzene by dechlorination with potassium-sodium alloy

Dechlorination of hexachlorobenzene (HCB) was achieved by a liquid potassium–sodium (K–Na)-alloy. HCB in a cyclohexane/benzene solution (22 mmol/l, 4.67 g/l as chlorine) was dechlorinated by almost 100% after a 30-min reaction, indicating high reactivity of K–Na alloy and high proton donating power of cyclohexane. Decreasing orders of chlorobenzenes identified after a 15-min reaction, by amount were 1,2,3,4- > 1,2,3,5- > 1,2,4,5- for tetrachlorobenzenes, 1,2,4- > 1,2,3- > 1,3,5- for trichlorobenzenes, and 1,4- > 1,3- > 1,2- for dichlorobenzenes. It was hypothesized that once one chlorine atom in HCB was replaced with a proton, the adjacent chlorine atom to the proton tended to be replaced with another hydrogen atom. A total of 63 PCBs formed via the Wurtz–Fittig reaction were identified as by-products in the sample after a 15-min reaction. Among PCBs found, 2,3^′,4^′,5-tetrachlorobiphenyl, which was a product from 1,2,4-trichlorobenzene formed via the Wurtz–Fittig reaction, was detected in relatively high concentration (48.9 nmol/ml). The sample obtained from a reaction mixture after 30 min contained only 14 PCBs in trace amounts, indicating that the PCBs formed were also further dechlorinated by K–Na alloy. Non-chlorinated compounds––such as methylbenzene, dimethylbenzene, dimer of tetrahydrofuran, and dicyclohexyl (dimer of cyclohexane)––were also identified in the samples. A method using K–Na alloy developed in the present study dechlorinated satisfactorily HCB at room temperature.     

Polychlorinated dibenzo-p-dioxins and dibenzofurans in invertebrate animals from a rural beach in Japan

PCDDs and PCDFs were analyzed by high resolution GC MS in several invertebrate animals collected from a rural beach in Japan. PCDDs and PCDFs were detected in all samples. Total concentration of PCDDs and PCDFs ranged 8.8–120 pg g⁻¹ wet and 3.5–38 pg g⁻¹ wet, respectively. TEQs of invertebrate animals examined ranged from 0.048 pg g⁻¹ wet in sea slug to 0.91 pg g⁻¹ wet in mussel. Isomer profiles in all samples were similar to each other despite of variety of species. Their major sources are estimated to be herbicides such as CNP and PCP, and combustion by using a statistical analysis of isomer profiles.