Inhibition of seawater on bisphenol A (BPA) degradation by Fenton reagents

To investigate bisphenol-A (BPA) degradation in seawater using Fenton reagents, changes in the BPA recovery and in the concentration of BPA metabolite, BPA-o-quinone in the three water samples; BPA free deionizad water (control water), 3% aq. NaCl and seawater as a function of time after BPA fortification in the presence of radical oxygen species (ROS) at 20 degrees C were investigated. The BPA recoveries were lower in both 3% aq. NaCl and seawater than in the control water. The BPA recovery in aq. NaOCl decreased as a function of NaOCl concentration, indicating that BPA could be degraded by the potent radical ion (OCl-) at the concentration of above 2 microM. A BPA metabolite, BPA-o-quinone was formed in all the water samples after addition of ROS which was produced by Fenton reaction (reaction of 0.11 M H2O2 and 0.44 mM FeCl3.6H2O). These results indicated that BPA degradation could occur by an addition of ROS and further accelerated by the formation of OCl- in salt containing water samples. BPA recovery was the highest in seawater immediately after addition of Fenton reagents and the amount of BPA-o-quinone was very low, which suggests that seawater possesses an inhibitory system on BPA degradation. There was a positive correlation (p<0.01) between the fortified iron concentration and turbidity in seawater. Turbidity might be originated from iron-binding substances. Degradation threshold of BPA was observed when Fenton reaction was employed in seawater fortified with high amount of BPA. The present study suggested that iron trapping caused an inhibition on BPA degradation by Fenton reagents.     

Occurrence of organo-arsenicals in jellyfishes and their mucus

Water-soluble arsenic compound fractions were extracted from seven species of jellyfishes and subjected to analysis by high-performance liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICP-MS) for arsenicals. A low content of arsenic was found to be the characteristic of jellyfish. Arsenobetaine (AB) was the major arsenic compound without exception in the tissues of the jellyfish species and mucus-blobs collected from some of them. Although the arsenic content in Beroe cucumis, which preys on Bolinopsis mikado, was more than 13 times that in B. mikado, the chromatograms of these two species were similar in the distribution pattern of arsenicals. The nine species of jellyfishes including two species treated in the previous paper can be classified into arsenocholine (AC)-rich and AC-poor species. Jellyfishes belonging to Semaostamae were classified as AC-rich species.     

Urinary 8-hydroxy-2'-deoxyguanosine in inhabitants chronically exposed to arsenic in groundwater in Cambodia

Arsenic concentrations in hair and urine, and urinary levels of 8-hydroxy-2'-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage, were examined for inhabitants of the Mekong Basin in Kratie Province, Cambodia. Also, the arsenic levels of tube-well water were determined. Total arsenic concentrations in tube-well water ranged from <1 to 886 microg L(-1), and 44.8% of these exceeded the WHO drinking water guideline of 10 microg L(-1). Elevated levels of arsenic were observed in the human hair and urine, and also a significant positive correlation was observed between the concentrations in hair and urine. These results suggest that the inhabitants are chronically exposed to arsenic through drinking the tube-well water. Levels of urinary 8-OHdG were higher for the subjects with higher arsenic levels in hair and urine, suggesting that induction of oxidative DNA damage was caused by chronic exposure to arsenic in tube-well water for the inhabitants in Kratie Province. To our knowledge, this is the first report on the oxidative DNA damage caused by chronic exposure to arsenic in groundwater for the inhabitants in Cambodia.     

Evaluation of the physiology of miniature pig fed Shochu distillery waste using mRNA expression profiling

Journal of Material Cycles and Waste Management - Shochu distillery waste is the discarded material generated during Shochu production, and it has been used as feed for livestock. In this study, we...     

Specific biomagnification of polychlorinated dibenzo-p-dioxins and dibenzofurans in tufted ducks (Aythya fuligula), common cormorants (Phalacrocorax carbo) and their prey from Lake Shinji, Japan

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDDs/DFs) were detected in waterfowl such as common cormorants, tufted ducks, and their prey, namely fish and bivalves from Lake Shinji, Japan. The concentration of total PCDDs/DFs-TEQ was found to be higher in the muscle tissues of common cormorants than in those of tufted ducks. The results of hierarchical cluster analysis implied that the residue distribution pattern of PCDD/DF homologues was considerably different between these two species. Furthermore, biomagnification factors (BMFs) were estimated from bivalves as prey to tufted duck muscles as target organs. Despite the highest concentrations of 1,3,6,8- and 1,3,7,9-TeCDD in tufted ducks and their prey, however, the BMFs of these isomers were calculated to be lower than those of the toxic 2,3,7,8-substituted PCDDs/DFs. On the other hand, log BMF of toxic 2,3,7,8-substituted PCDDs/DFs were significantly higher for lower chlorinated isomers than those of the higher chlorinated isomers. The biota-sediment accumulation factors (BSAFs) of PCDDs/DFs were also estimated using shijimi clam and fish samples against sediment from Lake Shinji. The average BSAFs were estimated and ranged from 4.0×10⁻³ to 2.2×10⁻¹ and 2.0×10⁻⁴ to 2.0×10⁻¹ for bivalve and fish samples, respectively. Based on calculated BMFs and BSAFs, the total PCDD/DF-TEQ levels in the tufted duck were estimated to have been lowest (2.0 pg TEQ/g dry weight basis) in 1947 and highest (9.8 pg TEQ/g) in 1971.     

Pharyngeal aspiration of single-wall carbon nanotubes aggravates allergic reaction to inhaled ovalbumin in mice

Single-wall carbon nanotubes are a major type of nano-objects that have industrial applications such as fuel cells. In this study, four types of single-wall carbon nanotubes and their abilities to aggravate allergic reactions were examined: those containing Fe, those containing Ni, and the corresponding purified metal-free ones. These were administered to mice via pharyngeal aspiration. Subsequently, the mice inhaled ovalbumin a total of eight times over three weeks. After inhalation of ovalbumin, the concentrations of total immunoglobulin E and ovalbumin-specific immunoglobulin E in serum increased in mice treated with purified metal-free and Fe containing single-wall carbon nanotubes while those containing Ni did not affect total and ovalbumin-specific immunoglobulin E levels. Additionally, the purified metal-free and Fe containing nanotubes caused the gene expression of heme oxygenase-1, chemokine (C-X-C motif) ligand 2, and tumor necrosis factor-α, suggesting that some kinds of single-wall carbon nanotubes have the potential to aggravate allergic reactions via oxidative stress and inflammation. Incorporated metals do not seem to be involved in the aggravation of allergic reactions. Other physical properties, such as fiber length and aggregation state, may be involved in enhancing allergic reactions.     

Validation of modeling approach to evaluate congener-specific concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans in air and soil near a solid waste incinerator

A concise modeling approach using long-term averaged meteorological data was developed to estimate site-specific concentrations of congeners of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) near a solid waste incinerator. This approach consists of calculation of atmospheric dispersion, dry and wet deposition of gaseous and particle-bound congeners, and non-steady-state concentrations in soil. The predictability of this approach was evaluated by comparison of calculated concentrations of congeners in soil with those measured at eight locations near a municipal solid waste incinerator (MSWI). The variation of these concentrations due to variability of meteorological parameters is small. A considerable number of mean values show good agreement with measured concentrations within a factor of three. The reasonable agreement between calculated and measured concentrations indicates that algorithms for the calculation of vapor-phase deposition and non-steady-state concentrations in soil must be included in the modeling approach for an accurate estimation of the concentrations of congeners of PCDD/Fs emitted from MSWIs to the atmosphere. For a detailed estimation of site-specific concentrations, it is important to specify the bulk density of soil in the evaluated area, together with meteorological parameters.     

Vegetation monitoring using diferent scale of remote sensing data

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A sex pheromone component novel to Ostrinia identified from Ostrinia latipennis (Lepidoptera: Crambidae)

Summary. Extracts from the sex pheromone gland of Ostrinia latipennis (Lepidoptera: Crambidae) were analyzed by gas chromatography-electroantennographic detection (GC-EAD) and GC-mass spectrometry. Only an EAD-active compound was detected in the extract, and it was identified as (E)-11-tetradecenol (E11-14:OH). In a wind-tunnel bioassay, E11-14:OH elicited a series of mate finding behaviors from males, although it was far less active than virgin females and crude extract of the pheromone gland. The attractiveness of E11-14:OH to O. latipennis males was confirmed by field trapping experiments. Based on these findings, we concluded that E11-14:OH, which is novel to the genus Ostrinia, is a major component of the sex pheromone in O. latipennis. The significance of the use of alcohol in place of the usual acetates in Ostrinia is discussed in relation to the pheromone biosynthesis system. Received 9 December 1999; accepted 14 March 2000     

Levels of total cyanide and NaCl in surface waters adjacent to road salt storage facilities

Concentrations of Na, Cl and total cyanide (simple+complex forms of cyanide) in surface waters adjacent to uncovered, outdoor sand-salt storage facilities were monitored for the calendar year 1988. Runoff of deicing salt from these unprotected sand-salt piles resulted in Cl concentrations up to 13,500 mg liter(-1) in surrounding surface waters indicating substantial leaching of road salt from sand-salt storage lots. The use of sodium hexacyanoferrate (II) as an anti-caking agent in road salt resulted in up to 200 microg liter(-1) total cyanide (CN) in surface waters adjacent to sand-salt piles. Concentrations of Na and Cl were highest during the summer months whereas the concentrations of total CN were highest during the autumn months. The observed concentrations of total CN were less than the calculated maximum concentrations based on total CN content of pure road salt indicating that sodium hexacyanoferrate(II) was being adsorbed during overland flow onto soils and/or sediments of the wetlands. A laboratory adsorption study using five soils and a road salt solution showed that the soils adsorbed from 25 to 83% of the sodium hexacyanoferrate(II) present in the soil-road salt suspensions. The percentage of sodium hexacyanoferrate(II) adsorbed on soils increased with decreasing soil pH.