Biodegradation of toxic chemicals in Guayanilla Bay,Puerto Rico

Studies were conducted to assess the factors that may influence the rate and extent of biodegradation of biphenyl, naphthalene, phenanthrene, pentachlorophenol (PCP) and p-nitrophenol in water samples collected from the Guayanilla Bay (18 degrees N; 67.45 degrees W), southwest of Puerto Rico. In vitro studies mediated slow degradation of biphenyl, naphthalene and phenanthrene substrates by natural microbial flora present in the Bay. Addition of KNO(3) as a source of inorganic N greatly enhanced the degradation of phenanthrene but not of naphthalene, suggesting that effects on degradation due to nutrient limitation were compound specific. The rate and extent of degradation of naphthalene and PCP were higher in water samples collected closer to the source of contamination, i.e. the petrochemical complex. The identity of a phenanthrene degrading bacterium, previously identified by conventional phenotypic method (Zaidi et al., Utilizing Nature's Advanced Materials, Oxford Unviersity Press, 1999) as Alteromonas sp., was confirmed by partial DNA sequencing of the small subunit rRNA gene.     

Spatio-temporal distribution and characteristics of PAHs in sediments from Masan Bay, Korea

The distribution of polycyclic aromatic hydrocarbons (PAHs) has been investigated in the surface and core sediments from Masan Bay, Korea. Total PAHs in the surface sediments ranged from 207 to 2670 ng/g dry weight with a mean value of 680 ng/g. Qualitative similarity and quantitative difference between inner and outer bay indicate that the main sources of PAHs are located in the inner bay and outer bay is also affected by the same sources. Vertical distribution of PAHs revealed that three distinctive stages could be differentiated with the help of PCA analysis. The highest concentration (industrialization stage) appeared between late 1950s and 1980, which was 10 years later than other developed countries. A strong pyrolytic source fingerprint has been detected with slight influence of petrogenic sources, and diagenetic PAH, perylene also contributed. Total organic carbon normalized PAHs (sum of 13 PAHs, 8.85-88.0 microg/g OC) were under the threshold effects concentration (TEC, 290 microg/g OC).     

Assessment of butyl- and phenyltin pollution in the coastal environment of Korea using mussels and oysters

Butyl- and phenyltin residues in bivalves were quantified around the coast of Korean peninsula in 1995–1998 and 2001. Butyltin compounds were detected at all the sites surveyed, whereas phenyltins were detected at 41 out of 67 sites in 1995–1998. Tributyltin (TBT) concentrations in bivalves ranged 48–2800 ng Sn/g on dry weight basis. Triphenyltin (TPT) concentrations ranged <3–1820. The mean TPT concentration was 3.5 times less than that of TBT. Spatial distribution of TBT was closely related to boating and dry-docking activities. TPT concentration in bivalves showed significant correlation with TBT. Concentrations of TBT in bivalves, 2001 are not significantly changed compared to those in 1995–1998. However, TPT concentrations in bivalves steeply decreased in 2001. High concentration of TBT and lesser extent TPT and their nation-wide distribution indicate that organotins are one of major organic pollutants in the marine environment of Korea.     

新疆西天山(南段)区域地球化学异常特征

西天山（南段）地区地处伊犁亚板块南缘活动带和塔里木板块边缘活动带内.向北突出呈弧形展布的近东西向主干断裂控制本区地层、岩浆岩及地球化学异常的分布.主体为志留、泥盆系富含碳质的碎屑岩-碳酸盐岩沉积.西天山（南段）主要成矿元素及其伴生元素集中在志留系、泥盆系和石炭系中,因而它们是研究区内最有潜力的找矿层位.志留系Au、As、Sb、Sn、Zn、Cr、Ni、Co、Ti富集,微量元素分布不均匀,元素组合多样,局部地段有富集成矿的趋势,地球化学图上有明显的Au、As、Sb、Hg、Cu的单元素异常或多元素的组合异常出现;泥盆系总体地球化学背景偏高,空间分布不均匀,元素组合复杂.富集元素有Au、As、Sb、Hg,有多元素的综合异常显示.根据区内元素异常分布、组合类型及控制异常分布的主要地质因素,将本区划分为4条综合异常带（9条亚带）.     

Radiocesium reaction with illite and organic matter in marine sediment

The mineralogical effect on the (137)Cs reaction with marine sediment has not been systematically studied yet, even though illite has been known to adsorb Cs preferentially on its frayed edge sites in a low Cs concentration. Ninety-three marine sediment samples were collected near Yangnam, Korea for quantitative X-ray-diffraction (XRD), gamma-ray, and total organic carbon (TOC) analysis. Illite content was in the range of 0-23 wt.% and those of (137)Cs and TOC were minimum detectable activity (MDA) approximately 7.19 Bq/kg-dry and approximately 3.32%, respectively. The illite content in the marine sediment showed a good relationship with the (137)Cs content (R(2)=0.69), but with an increase in the illite content, the relationship became less linear. This trend can be clearly shown in two groups of samples with different size fractions (< and >5Mdvarphi). For the samples of larger particle sizes (low contents of illite), the relationship is linear, but for the samples of the smaller particle sizes (high illite content) it is less linear with a decreased slope, indicating that increase in illite content does not significantly contribute to the fixation of (137)Cs in marine sediment. Rather, the TOC has a more linear relationship with (137)Cs content with no slope change in all particle size ranges. This may indicate that humic materials in marine sediment block the access of (137)Cs to the frayed edge site and reduces the adsorption of (137)Cs on illite and that the organic materials in marine sediment play more important roles in adsorbing Cs than illite.     

The accumulation of radiocesium in coarse marine sediment: effects of mineralogy and organic matter

The controlling factors affecting the accumulation of (137)Cs in marine sediment have not been investigated in detail, especially in coarse grained sediment. Eighty eight coarse marine sediment samples near Wuljin, Korea, were characterized by quantitative X-ray-diffraction (XRD), gamma-ray, and total organic carbon (TOC) analysis. Those factors were then compared. The grain size was in the range of -0.48 to 3.6Mdphi corresponding to sand grains. TOC content was in the range of 0.06-1.75%, and the concentration of (137)Cs was 相似文献