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.     

Time trends of perfluorinated compounds from the sediment core of Tokyo Bay, Japan (1950s-2004)

Perfluorinated compounds (PFCs) were detected in sediment core samples collected in Tokyo Bay to reveal their time trends. The core sample deposited during 1950s-2004 was divided into two- to three-year intervals and the concentrations of 24 types of PFCs were determined. Perfluorooctane sulfonate (PFOS) decreased gradually from the early 1990s and its precursor decreased rapidly in the late 1990s, whereas perfluorooctanoic acid (PFOA) increased rapidly. The observed trends were regarded as a reflection of the shift from perfluorooctyl sulfonyl fluoride (PFOSF)-based products to telomer-based products after the phaseout of PFOSF-based products in 2001. The branched isomers of perfluoroundecanoic acid (PFUnDA) and perfluorotridecanoic acid (PFTrDA) were detected in the sample with its ratio of linear-isomer/branched-isomer concentrations decreasing. In this study, we revealed that the sediment core can serve as a tool for reconstructing the past pollution trend of PFCs and can provide interesting evidence concerning their environmental dynamics and time trend.     

Carbon Sequestration by Carbonization of Biomass and Forestation: Three Case Studies

We proposed the carbon sink project called “Carbon Sequestration by Forestation and Carbonization (CFC),” which involves biomass utilization and land conservation by incorporating the products of biomass carbonization into the agents for soil improvement, water purification, etc. Our purpose was to demonstrate the potential of the CFC scheme for carbon sequestration, particularly carbon storage in soil. Case studies were conducted in both developing and developed countries. 1. In southern Sumatra, Indonesia, 88,369 Mg-C year⁻¹ of wood residue from a plantation forest and excess bark from a pulp mill would be converted into 15,571 Mg-C year⁻¹ of the net carbon sink by biochar for soil improvement. The fixed carbon recovery of the system is 21.0%. 2. In a semiarid region in western Australia, the carbonization of wood residue was incorporated with multipurpose projects of a mallee eucalyptus plantation that involved the function of salinity prevention. During the project period of 35 years, the total carbon sink would reach 1,035,450 Mg-C with 14.0% by aboveground biomass, 33.1% by belowground biomass and 52.8% by biochar in soil. 3. In southern Kyushu, Japan, the study was focused on the effective use of surplus heat from a garbage incinerator for carbonizing woody materials. Sawdust of 936.0 Mg-C year⁻¹ would be converted into the net carbon sink of 298.5 Mg-C year⁻¹ by carbonization, with the fixed carbon recovery of the system being 31.9%. Consequently, the CFC project could encourage the creation of a carbon sink in soil. However, we recognize that the quality standard of biochar, the stability of biochar in soil, and the methods for monitoring biochar utilization must be clarified before incorporating biochar carbon into the carbon credit system. Throughout this article (except for diagrams and in citation details) carbonized biomass is, with the authors'agreement, called ‘biochar’ in lieu of the commonly used but misleading word ‘charcoal’ (Editor).     

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.     

微激光烧蚀电感偶合等离子体质谱多元素分析环境物质

采用微激光烧蚀电感偶合等离子体质谱分析了环境物质中的11种元素(镁、钾、钙、铁、镍、铜、锌、铷、铯、钡、铅)。将日本国立环境研究所(NIES)认证标准物质(CRM)No.3小球藻(chlorella),No.7茶叶,No.9果囊马尾藻(sargasso)及国家标准技术研究所(NIST)标准参考物质(SRM)1573西红柿叶和1568小麦粉,分别用基体相似的NIESNo.1胡椒藤和No.10-c小麦粉校准各元素测定灵敏度。让薄薄一层粉末状样品紧紧粘在一小块粘胶纸上,不需要另外的样品制备。测定方法有较高的灵敏度,且其分析过程简单快速。      

Chemical content and source apportionment of 36 heavy metal analysis and health risk assessment in aerosol of Beijing

The concentration levels of 36 airborne heavy metals and atmospheric radioactivity in total suspended particulate (TSP) samples were measured to investigate the chemical characteristics, potential sources of aerosols, and health risk in Beijing, China, from September 2016 to September 2017. The TSP concentrations varied from 6.93 to 469.18 μg/m³, with a median of 133.97 μg/m³. The order for the mean concentrations of heavy metals, known as hazardous air pollutants (HAPs), was as follows: Mn > Pb > As > Cr > Ni > Se > Cd > Co > Sb > Hg > Be; Non-Designated HAPs Metals: Ca > Fe > Mg > Al > K > Na > Zn > P > Ba > Ti > Cu > Sr > B > Sn > I > V > Rb > Ce > Mo > Cs > Th > Ag > U > Pt. The median concentration of As was higher than China air quality standard (6 ng/m³). The gross α and β concentration levels in aerosols were (1.84?±?1.59) mBg/m³ and (1.15?±?0.85) mBg/m³, respectively. The enrichment factor values of Cu, Ba, B, Ce, Tl, Cs, Pb, As, Cd, Sb, Hg, Fe, Zn, Sn, I, Mo, and Ag were higher than 10, which indicated enriched results from anthropogenic sources. Pb, As, and Cd are considered to originate from multiple sources; fireworks released Ba during China spring festival; Fe, Ce, and Cs may come from stable emissions such as industrial gases. The health risks from anthropogenic metals via inhalation, ingestion, and dermal pathway were estimated on the basis of health quotient as well as the results indicated that children faced the higher risk than adults during the research period. For adults, the health risk posed by heavy metals in atmospheric particles was below the acceptable level.

     

International recycling firm joint ventures and optimal recycling standards

Environmental Economics and Policy Studies - In this paper, we consider a Southern economy consisting of an upstream duopoly market for recycled materials and a downstream perfectly competitive...     

GIS-based source identification and apportionment of diffuse water pollution: perfluorinated compound pollution in the Tokyo Bay basin

To efficiently reduce perfluorinated compound (PFC) pollution, it is important to have an understanding of PFC sources and their contribution to the pollution. In this study, source identification of diffuse water pollution by PFCs was conducted using a GIS-based approach. Major components of the source identification were collection of the monitoring data and preparation of the corresponding geographic information that was extracted from a constructed GIS database. The spatially distributed pollution factors were then explored by multiple linear regression analysis, after which they were visually expressed using GIS. Among the 35 PFC homologues measured in a survey of the Tokyo Bay basin, 18 homologues were analyzed. Pollution by perfluorooctane sulfonate (PFOS) was explained well by the percentage of arterial traffic area in the basin, and the 84% variance of the measured PFOS concentration was explained by two geographic variables, arterial traffic area and population. Source apportionment between point and nonpoint sources was conducted based on the results of the analysis. The contribution of PFOS from nonpoint sources was comparable to that from point sources in several major rivers flowing into Tokyo Bay. Source identification and apportionment using the GIS-based approach was shown to be effective, especially for ubiquitous types of pollution, such as PFC pollution.     

Assessment of the aerosol water content in urban atmospheric particles by the hygroscopic growth measurements in Sapporo,Japan

Aerosol water content (AWC) of urban atmospheric particles was investigated based on the hygroscopic growth measurements for 100 and 200 nm particles using a hygroscopicity tandem differential mobility analyzer in Sapporo, Japan in July 2006. In most of the humidogram measurements, presence of less and more hygroscopic mode was evident from the different dependence on relative humidity (RH). The volume of liquid water normalized by that of dry particle (V_w(RH)/V_dry) was estimated from the HTDMA data for 100 and 200 nm particles. The RH dependence of V_w(RH)/V_dry was well represented by a fitted curve with a hygroscopicity parameter κ_eff. The κ_eff values for 200 nm particles were in general higher than those for 100 nm particles, indicating a higher hygroscopicity of 200 nm particles. Based on the κ_eff values, the volume mixing ratios of water-soluble inorganic compounds (ammonium sulfate equivalent) were estimated to be on average 31% and 45% for 100 and 200 nm particles, respectively. The diurnal variation of κ_eff, with relatively higher values in the noontime and nighttime and lower values in the morning and evening hours, was observed for both particle sizes. The V_w(RH)/V_dry values under ambient RH conditions were estimated from κ_eff to range from 0.05 to 2.32 and 0.06 to 2.43 for 100 nm and 200 nm particles, respectively. The degree of correlation between κ_eff and V_w(RH)/V_dry at ambient RH suggests a significant contribution of the variation of κ_eff to atmospheric AWC in Sapporo.     

Gasification and smelting system using oxygen blowing for plastic waste including polyvinyl chloride

A new type of waste gasification and smelting system using oxygen blowing based on high-temperature metallurgy, was developed by Sumitomo Metals, Japan. This system can steadily gasify and melt not only municipal waste, but also plastic waste and polyvinyl chloride (PVC) waste by using a top-blow oxygen lance together with sideways-blow oxygen lances. As a result of gasification in the high-temperature reducing atmosphere and rapid gas cooling, dioxin-free, high-calorie purified gas was produced. Ash components in the wastes were smelted in a high-temperature reducing atmosphere, and high-quality slag free of heavy metals was produced. Most of the chlorine in the wastes was converted into hydrogen chloride in the off gas. The hydrogen chloride can be recovered as hydrochloric acid or chlorine, which are recyclable to PVC manufacturing.