Observations of aerosol-bound ionic compositions at Cheju Island,Korea

To investigate the regional cycle of aerosols and their ionic constituents, three field intensive campaigns were conducted during fall and winter of 1997 and spring of 1998. The concentrations of most ionic species were found to decrease significantly across fall, winter, and spring such that the sum for all cation (and anion) species of each season is computed as: 193 > 96 > 73.7 nequiv m(-3) (and 240 > 104 > 51.5 nequiv m(-3)). To examine the fundamental characteristics of aerosol compositions in the study area, we conducted correlation analysis in various manners. The results indicated that the concentrations of major ionic species were strongly affected by some meteorological parameters including wind speed. It was also seen that relative strengths of correlations between important parameters (e.g., between wind speed and most of major inorganic species) maintain close relationships with the factors associated with the air mass origin. In addition, the results of factor analysis indicated the existence of at least three major sources in the study area which include: sea-salt aerosol, secondary aerosol, and organic aerosol component. The springtime occurrence of unexpectedly low concentrations of most ionic constituents is found to sensitively reflect the influence of the inflow of southeasterly winds that prevailed during spring, while it is not common for that season of the year. Because most of those changes are closely tied with the variabilities in the regional circulation patterns for each measurement period, assessment of the ionic composition in concert with the temporal variations of meteorological conditions provided valuable insights into the source signals of different air masses that passed by the study area.     

Long-term effects of fertilization on the forms and availability of soil phosphorus in rice paddy

The changes in total P accumulation and P compounds with time in the plough layer in a paddy soil in southern Korea were investigated in relation to the continuous application of chemical fertilizers (NPK), straw based compost (Compost), combination these two (NPK+Compost) for 31 years. Continuous fertilization increased the total and inorganic P contents in plough layers. In NPK, inorganic P fraction did not change with time, but organic P content increased significantly. Long-term application of chemical fertilizer together with compost accelerated the decrease in the organic P fraction, presumably due to promoting microbial activity in the plow layer, and then increased significantly inorganic P fraction. Compost application decreased the residual P and Fe-P fractions and then increased inorganic P fraction, in spite of continuous compost application. Increase in total, inorganic and extractable P with time may be closely related to the increase in the availability of accumulated P for rice growth.     

Volatility of propoxur from different surface materials commonly found in homes

The purpose of this study was to determine the volatilization rates of propoxur from different surface materials commonly found in homes, and to conduct field measurements under ventilated and non-ventilated conditions. Since it is known that temperature, humidity and constant air flow most significantly affect volatility, various surface materials were sprayed using a constant amount of propoxur under the controlled conditions of an exposure chamber. Acetonitrile was used to desorb both XAD-2 resin that collected airborne propoxur and surface materials containing propoxur residue. HPLC was used to analyze propoxur concentrations. Based on multiple regression models, temperature most significantly affected volatility, followed by humidity. Volatilization rates of propoxur were highest from quartz surfaces and lowest from glass. Interaction was most readily found on glass surfaces based on humidity-air flow and humidity-temperature factors. In field applications, propoxur was sprayed in a room under two conditions with ventilation and without in order to measure the concentrations of propoxur in the air and on a quartz surface. Findings showed both airborne and settled concentrations peaked after a half hour then decreased under both conditions, both more sharply in the ventilated room. Under both conditions, no propoxur was detected on the quartz surface after three and a half hours but airborne concentrations remained detectable after thirty-three and one half hours. We conclude that to maintain good air quality, ventilation is important and special care must be taken when spraying insecticides on different surfaces.     

Catalytic wet oxidation of ammonia: why is N2 formed preferentially against NO3 -?

The role of catalyst and the reason for the preferential formation of N(2) in the catalytic oxidation reaction of ammonia in water over a Ru (3wt.%)/TiO(2) catalyst were elucidated. It was verified that the catalyst in the reaction had no direct relevance to the selective formation of N(2), but was responsible only for the oxidation of aqueous ammonia, NH(3)(aq), finally giving a molecule of nitrous acid. The preferential production of N(2) was experimentally demonstrated due to the homogeneous aqueous phase reaction of the nitrous acid-dissociated NO(2)(-) with NH(4)(+) ions. Even under the highly oxidizing condition, NO(2)(-) was much more likely to react with NH(4)(+) to form N(2) than being oxidized over the catalyst to NO(3)(-) as long as NH(4)(+) was available in solution.     

Formation of disinfection by-products in chlorinated swimming pool water.

The formation of five volatile disinfection by-products (DBPs: chloroform, bromodichloromethane, chloral hydrate, dichloroacetonitrile, and 1,1,1-trichloropropanone) by the chlorination of the materials of human origin (MHOs: hair, lotion, saliva, skin, and urine) in a swimming pool model system was examined. Chlorination reactions took place with a sufficient supply of chlorine residuals (0.84 mg Cl2/l < total chlorine < 6.0 mg Cl2/l) in 300 ml glass bottles containing either ground water or surface water as a reaction medium at 30 degrees C and pH 7.0, for either 24 or 72 h. A longer reaction period of 72 h or a higher content of organic materials led to the increased formation of DBPs. Of the DBPs formed by the reaction, chloroform was a major compound found in both ground and surface waters. The formation of chloroform and bromodichloromethane per unit total organic carbon (TOC) concentration was suppressed when all types of MHOs were added to the surface water that already contained DBP precursors such as humic substances. However, the formation of dichloroacetonitrile was promoted, probably due to the increased degradation reactions of nitrogen-containing compounds such as urea and proteins of human origin. In conclusion, the materials of swimmers' origin including hair, lotion, saliva, skin, and urine add to the levels of DBPs in swimming pool water, and any mitigation measures such as periodic change of water are needed to protect swimmers from elevated exposures to these compounds.     

烟酰胺降解菌的筛选及其降解特性

采用HPLC对某烟酰胺生产废水的主要成分进行分析，并模拟废水中的主要成分烟酰胺（nicotinamide）的浓度，对以烟酰胺为唯一碳源配制的培养基进行降解实验，获得有较佳降解率和生长能力的菌株YSI-1和YSI-2。结果表明．YSI菌株的混合菌降解效果优于单株菌，混合菌在初始OD600值为0．4，pH为7．0时，对浓度为2000mg／L的烟酰胺降解2d的降解率可达32．8％。延长处理时间或提高菌种的初始OD600值，烟酰胺的去除率均有较大的增加。     

Biosynthesis of lipds in zooplankton from Saanich Inlet,British Columbia,Canada

Lipid analyses were carried out on various species of zooplankton captured in Saanich Inlet, British Columbia, Canada, during September, 1972. The amphipod Cyphocaris challengeri had the highest level of lipid, consisting mainly of wax esters. The copepod Calanus pacificus had moderate amounts of lipid, with triglyceride as the major neutral lipid. The euphausiid Thysanoessa raschii contained mainly triglyceride in its moderate levels of neutral lipid, while wax esters and, to a lesser extent, triglycerides were present in the very small levels of neutral lipid in the chaetognath Sagitta elegans. The major fatty alcohols in wax esters of both Cyphocaris challengeri and Calanus pacificus were 20:1 and 22:1, although notable differences were found in the major fatty acids. Biosynthetic studies showed that phospholipids were labelled faster than neutral lipids in all species with both (U-¹⁴C) glucose and (1-¹⁴C) palmitic acid as precursors. Only species containing significant amounts of wax esters in their neutral lipids incorporated substantial amounts of radio-activity from (1-¹⁴C) palmitic acid into wax esters in (i) living animals, (ii) preparations containing fragments of tissue, (iii) cell-free systems. All species incorporated added fatty alcohols into wax esters in preparations containing tissue fragments and in cell-free preparations. Both the fatty acid and fatty alcohols of the wax esters of both Calanus pacificus and S. elegans were labelled from (1-¹⁴C) palmitic acid, consistent with de novo biosynthesis of the esters. (1-¹⁴C) hexadecanol was incorporated into wax esters almost entirely in the fatty alcohol moiety. It is concluded that all species examined formed was esters when presented with preformed fatty alcohols, but only those species that had wax esters as a major component of the neutral lipids were capable of de novo biosynthesis of the lipids.     

METROPOLITAN GROWTH AND WATER MANAGEMENT IN LATIN AMERICA

This article discusses some recent developments in water management in Latin America. It is based on research done during the joint CEPAL/UNEP project on Water Development and the Environment. The author discusses the changes in water use occurring in Latin America in general, the contemporary relationship with the water resource in four major metropolitan centres, Bogotá, Colombia, Lima, Peru, and Sāo Paulo and Rio de Janeiro, Brazil. On the basis of the general and specific experiences described, general conclusions are drawn as to styles of water management current in the region and adjustments to the problem posed by the emergence of very large metropolitan concentrations of population and economic activity. Cet article reprend des développements récents en matière de gestion des ressources en eau en Amérique latine. II se base sur des recherches effectuées au cours de l'exécution du projet conjoint CEPAL/PNUE sur la mise en valeur des ressources en eau et de l'environnement. L'auteur discute des modifications intervenues dans l'utilisation des ressources en eau en Amérique latine en général et le rapport qui existe actuellement entre les ressources en eau et quatre centres principaux urbains (Bogota en Colombie, Lima au Pérou, et Sāo Paulo et Rio de Janeiro au Brésil). Sur la base des experiences générales et particulières décrites, des conclusions génèrales sont tirées quant aux modes de gestion actuelle des ressources en eau dans la région et aux améliorations apportées au problème créé par l'apparition d'énormes agglomérations urbaines à activité économique intense. Este artículo trata sobre algunos desarrollos recientes en la administración del uso de recursos de agua en Latinoamérica. El artículo está basado en la investigación realizada en el proyecto conjunto CEPAL/PNUMA sobre Desarrollo de Agua y el Medio Ambiente. El autor analiza los cambios que están ocurriendo en el uso de recursos de ague en Latinoamérica en general y las relaciones entre los recursos de agua y los usos en cuatro centros metropolitanos: Bogotá, Lima, Sāco Paulo y Rio de Janeiro. Basándose en descripciones de experiencias generales y específicas, se extraen conclusiones sobre los estilos de la administración de recursos de agua existentes en la región y sobre la solución a los problemas planteados por la emergencia de grandes concentraciones metropolitanas de población y actividad económica.