Shoichi Kunikane

Trace analysis of androgens and progestogens in environmental waters by ultra-performance liquid chromatography-electrospray tandem mass spectrometry.

A sensitive ultra-performance liquid chromatography-electrospray tandem mass spectrometry method, combined with solid-phase extraction and silica cartridge cleanup, was established for nine androgens (androstenedione, 19-nor-4-androstene-3,17-diol, androsterone, epiandrosterone, testosterone, methyltestosterone, trenbolone, nandrolone, stanozolol) and nine progestogens (progesterone, 17alpha-hydroxyprogesterone, 21alpha-hydroxyprogesterone, 6alpha-methyl-hydroxyprogesterone, 17alpha,20beta-dihydroxy-4-pregnene-3-one, megestrol acetate, norethindrone, norgestrel, medroxyprogesterone acetate) in environmental waters. For the various water matrices considered, the overall method recoveries were from 78 to 100%, and no apparent signal suppression was found. The method detection limits for the eighteen analytes in the influent, effluent and surface water samples were 0.20-50, 0.04-20 and 0.01-12 ng/L, respectively. This method was used to analyze the residual androgens and progestogens in the wastewater and surface water samples from Japan, and ten analytes (0.03 (medroxyprogesterone acetate)-1441 ng/L (androsterone)) were detected in the wastewater samples, and four analytes (0.06 (progesterone)-0.46 ng/L (androstenedione)) were detected in the surface water samples.

Simultaneous analysis of 16 sulfonamide and trimethoprim antibiotics in environmental waters by liquid chromatography–electrospray tandem mass spectrometry

A sensitive liquid chromatography-electrospray tandem mass spectrometry method combined with solid-phase extraction and silica cartridge cleanup was established for 16 sulfonamides and trimethoprim in various water matrices. Signal suppression of all target analytes in sewage treatment plant influent, effluent and river water was improved by this method developed in this study. The method detection limits for 17 analytes were 20-200 pg/L for influent, 16-120 pg/L for effluent and 8.0-60 pg/L for river water with overall mean recoveries of 62-102% in all studied matrices. This method was used to analyze residual sulfonamides and trimethoprim in wastewater and river samples from Japan, and 8 analytes (0.08 (sulfadimethoxine)-161 ng/L (sulfapyridine) in wastewater and 10 (0.03 (sulfamethizol)-8.9 ng/L (sulfaquinoxaline) in river samples were detected.

Simultaneous determination of tetracyclines and their degradation products in environmental waters by liquid chromatography-electrospray tandem mass spectrometry.

A sensitive method was developed for the trace determination of six tetracyclines and ten of their degradation products in influent, effluent, and river waters using liquid chromatography-electrospray tandem mass spectrometry detection, combined with Oasis hydrophilic-lipophilic balance (HLB) cartridge extraction and Oasis mixed-mode strong anion exchange (MAX) cartridge cleanup. Tetracyclines and their products were separated by liquid chromatography in 9.5min, and the instrument detection limits were generally between 0.03 and 0.1microg/L except for minocycline (0.5microg/L). The chromatograms were improved through the MAX cleanup and no apparent matrix effect was found. The recoveries of all the target compounds except for 4-epianhydrochlortetracycline and anhydrochlortetracycline (34-52%) were 75-120% for influent, 61-103% for effluent, and 64-113% for river waters. The method detection limits (MDLs) of the analytes varied in the range of 0.8-17.5ng/L in all studied matrices. The method was applied for the determination of tetracyclines and their products in a sewage treatment plant (STP) and surface waters in Beijing, China. Oxytetracycline (3.8-72.5ng/L), tetracycline (1.9-16.5ng/L), and five products including 4-epitetracycline, 4-epioxytetracycline, isochlortetracycline, anhydrotetracycline, and 4-epianhydrochlortetracycline (5.7-25.3ng/L) were detected in wastewater, while only oxytetracycline and tetracycline (2.2 and 2.1ng/L) were detected in surface water samples.

Formation of N-nitrosodimethylamine (NDMA) by ozonation of dyes and related compounds.

Formation of N-nitrosodimethylamine (NDMA) by ozonation of commercially available dyes and related compounds was investigated. Ozonation was conducted using a semi-batch type reactor, and ozone concentration in gas phase and the ozone gas flow were 10 mg L(-1) and 1.0 L min(-1), respectively. NDMA was formed by 15 min of ozonation of seven out of eight selected target compounds (0.05 mM) at pH 7. All the target compounds with N,N-dimethylamino functions were NDMA precursors in ozonation. The lowest and highest NDMA concentrations after ozonation of the target compounds were 13 ng L(-1) for N,N-dimethylformamide (DMF) and 1600 ng L(-1) for N,N-dimethyl-p-phenylenediamine (DMPD), respectively. NDMA concentrations after 15 min of ozonation of 0.05 mM methylene blue (MB) and DMPD increased with an increase in pH in its range of 6-8. The effects of coexisting compounds on NDMA concentrations after 15 min of ozonation of 0.05 mM MB and DMPD were examined at pH 7. NDMA concentrations after ozonation of MB and DMPD increased by the presence of 0.05 mM (0.7 mg L(-1) as N) nitrite (NO(2)(-)); 5000 ng L(-1) for MB and 4000 ng L(-1) for DMPD. NDMA concentration after MB ozonation decreased by the presence of 5mM tertiary butyl alcohol (TBA), a hydroxyl radical (HO.) scavenger, but that after DMPD ozonation was increased by the presence of TBA. NDMA concentrations after ozonation of MB and DMPD were not affected by the presence of 0.16 mM (5.3 mg L(-1)) hydrogen peroxide (H(2)O(2)). When 0.05 mM MB and DMPD were added to the Yodo and Tone river water samples, NDMA concentrations after 15 min of their ozonation at pH 7 increased compared with those in the case of addition to ultrapure water samples.

Application of real-time PCR assays to genotyping of F-specific phages in river water and sediments in Japan.

Genotyping of F-specific RNA phages is currently one of the most promising approaches to differentiate between human and animal fecal contamination in aquatic environments. In this study, a total of 18 river water and sediment samples were collected from the Tonegawa River basin, Japan, in order to describe the genogroup distribution of F-specific RNA and DNA phages using genogroup-specific real-time PCR assays. F-specific phages were detected in nine (100%) river water and six (67%) sediment samples. Eighty-five phage plaques were isolated from these samples and subjected to real-time PCR assays specific for the phages. F-specific RNA phages of human genogroups (II and III) were detected in 32 (38%) plaques, whereas those of animal genogroups (I and IV) were detected in 17 (20%) plaques. No correlation was observed between the genogroup distribution of F-specific RNA phages and the occurrence of human adenovirus genomes, suggesting that genotyping of the phages alone is inadequate for the evaluation of the occurrence of viruses in aquatic environments. SYBR Green-based real-time PCR assay revealed the presence of F-specific DNA phages in four (5%) plaques, which were further classified into two genogroups (fd- and f1-like phages) by sequence analysis. Thirty-two (38%) plaques were not classified as the F-specific phage genogroups, indicating the limited applicability of these real-time PCR assays to a wide range of aquatic environmental samples worldwide.

Modelling climate change impacts on the seasonality of water resources in the Upper Ca River Watershed in Southeast Asia.

The impact of climate change on the seasonality of water resources in the Upper Ca River Watershed in mainland Southeast Asia was assessed using downscaled global climate models coupled with the SWAT model. The results indicated that temperature and evapotranspiration will increase in all months of future years. The area could warm as much as 3.4°C in the 2090s, with an increase of annual evapotranspiration of up to 23% in the same period. We found an increase in the seasonality of precipitation (both an increase in the wet season and a decrease in the dry season). The greatest monthly increase of up to 29% and the greatest monthly decrease of up to 30% are expected in the 2090s. As a result, decreases in dry season discharge and increases in wet season discharge are expected, with a span of ±25% for the highest monthly changes in the 2090s. This is expected to exacerbate the problem of seasonally uneven distribution of water resources: a large volume of water in the wet season and a scarcity of water in the dry season, a pattern that indicates the possibility of more frequent floods in the wet season and droughts in the dry season.

Perchlorate: Origin and Occurrence in Drinking Water

Perchlorate is both a naturally occurring and a man-made chemical. Perchlorate compounds, such as perchlorate salts and perchloric acid, are used in various products, including rocket/missile propellants, munitions, explosives, fireworks, airbag initiators, and road flares. Perchlorate is known to interfere with iodine uptake by the thyroid gland. Since 1997, perchlorate has been detected in water as well as in various media (e.g., soil, food, milk, beverages, and plants). The occurrence of perchlorate was initially reported in the United States, but it is currently reported to be present in other countries. Anthropogenic perchlorate is considered the main source of perchlorate contamination in the environment. The potential sources are manufacturers of perchlorate and perchlorate-containing products and those using perchlorate in operations, alongside other users of perchlorate-containing products. Perchlorate is also known to be present naturally in many groundwaters. This article reviews the origins of perchlorate and examples of its presence as a contaminant in drinking water, groundwater, and surface water. The occurrence of perchlorate in the drinking water of water systems in several countries is also summarized, and perchlorate concentrations in various types of bottled water are described.

Effects of introducing energy recovery processes to the municipal solid waste management system in Ulaanbaatar, Mongolia

Currently, most developing countries have not set up municipal solid waste management systems with a view of recovering energy from waste or reducing greenhouse gas emissions. In this article, we have studied the possible effects of introducing three energy recovery processes either as a single or combination approach, refuse derived fuel production, incineration and waste power generation, and methane gas recovery from landfill and power generation in Ulaanbaatar, Mongolia, as a case study. We concluded that incineration process is the most suitable as first introduction of energy recovery. To operate it efficiently, 3Rs strategies need to be promoted. And then, RDF production which is made of waste papers and plastics in high level of sorting may be considered as the second step of energy recovery. However, safety control and marketability of RDF will be required at that moment.

Managing environmental performance in industrial zones: case studies in Ho Chi Minh City, Vietnam

Using government records, data from hazardous waste treatment companies, and on-site surveys, we evaluated the effectiveness of the current industrial solid waste management system in Ho Chi Minh City (HCMC), which was established according to the revised Law on Environmental Protection of 2005 and related regulations. In addition, we examined the relationship between the management system and environmental compliance by companies. Attention was paid to the classification of industrial solid waste, its amount finally disposed, and the cost of its disposal in HCMC. The results showed: one, the incoherence of the revised law and regulations in solid waste management caused serious pressure on landfills, and two, the implementation of the regulations has been neglected at all aspects of the current management system due to low levels of companies’ registration and reporting, as well as low levels of compliance among companies in industrial zones. A solution for dealing with the current problems is proposed.

Isolation of Bacteria Lysing Musty Odor Producing Alga Phormidium tenue and Its Lytic Characteristics

An alga-lytic bacterium, Pseudomonas KA6, was isolated from Lake Kasumigaura by a double-layer method. the filtrate of Pseudomonas KA6 culture lysed Phormidium tenue promptly. It was found that the growth of P. tenue is controlled by the addition of the filtrate 5 % and more. The lysis of P. tenue occurred efficiently at 25-35°C and pH 7-9. the cell of P. tenue in the stationary and endogenous phases was lysed promptly compared with that of P. tenue in the logarithmic phase. The filtrate lysed Oscillatoria sp. and Anabaena planktonica immediately as well as P. tenue; however, the filtrate lysed Microcystis aeruginosa slowly, and did not lyse green algae and diatoms. It was suggested that lytic compounds in the filtrate of KA6 culture affect only cyanobacteria in a water environment.