西安市文教区表层土壤中PAHs来源及风险分析

文教区土壤环境质量直接影响学生以及职工的身体健康。本研究应用高效液相色谱仪对采集的西安市文教区表层土壤样品中的16种优控多环芳烃(PAHs)进行含量检测,分析其组分特征、来源及健康风险。结果表明,西安市文教区表层土壤中∑PAHs含量为0.290~4.147μg/g,平均值为1.515μg/g,7种致癌多环芳烃的含量为0.079~2.093μg/g,均值为0.593μg/g,土壤PAHs污染较为严重。其中4环的高环PAHs为土壤PAHs污染的主要物质,平均占∑PAHs含量的40.72%。源解析结果表明西安市文教区表层土壤中PAHs主要来源于石油燃烧、煤及生物质等的不完全燃烧。终生癌症风险评价表明西安市文教区表层土壤中PAHs污染对其生活在周围的人群产生的终生致癌风险性较小,但71.4%的样点达到严重污染水平,产生的间接影响应引起足够重视。     

The Chemistry of Soils, Rocks and Plant Bioindicators in Three Ecosystems of the Holy Cross Mountains, Poland

In June of 2000, biogeochemical study was carried out in three ecosystems of the Holy Cross Mountains (south-central Poland). This paper presents element concentrations and stable sulfur (and in one site lead) isotope ratios in rocks, detailed soil profiles, and plant bioindicators including epiphytic lichen Hypogymnia physodes (L.) Nyl., mosses (Pleurozium schreberi (Brid.) Mitt., Hypnum cupressiforme Hedw. S. Str., Hylocomium splendens (Hedw.) B.S.G.), Scots pine (Pinus sylvestris L.), common birch (Betula pendula Roth.), aspen (Populus tremula L.) and English oak (Quercus robur L.). Chemical analyses were performed with ICP-AES and AAS methods in the accredited laboratory (Central Chemical Laboratory of the Polish Geological Institute in Warsaw). The principal objective of this study was to compare the chemical composition of rocks, soils and selected plant bioindicators between investigation sites using the same methods of sample collection, preparation and analyses. The results of this study have shown that there is a high variability in concentrations of elements in plant bioindicators from the same sites that can not be explained only by soil properties or anthropogenic influence. This conclusion indicates that for biomonitoring purposes (especially with vascular plants) we cannot neglect individual features of the species examined.     

Effects of the new nitrification inhibitor 3,4-dimethylpyrazole phosphate (DMPP) on nitrate and potassium leaching in two soils

In this study, soil column was used to study the new nitrification inhibitor 3,4-dimethylpyrazole phosphate (DMPP) on nitrate (NO3--N) and potassium (K) leaching in the sandy loam soil and clay loam soil. The results showed that DMPP with ammonium sulphate nitrate (ASN) ((NH4)2SO4 and NH4NO3) or urea could reduce NO3--N leaching significantly, whereas ammonium (NH4 -N) leaching increased slightly. In case of total N (NO3--N NH4 -N), losses by leaching during the experimental period (40 d) were 37.93 mg (urea), 31.61 mg (urea DMPP), 108.10 mg (ASN), 60.70 mg (ASN DMPP) in the sandy loam soil, and 30.54 mg (urea), 21.05 mg (urea DMPP), 37.86 mg (ASN), 31. 09 mg (ASN DMPP) in the clay loam soil, respectively. DMPP-amended soil led to the maintenance of relatively high levels of NH4 -N and low levels of NO3--N in soil, and nitrification was slower. DMPP supplementation also resulted in potassium leached less, but the difference was not significant except the treatment ASN and ASN DMPP in the sandy loam soil. Above results indicate that DMPP is a good nitrification inhibitor, the efficiency of DMPP seems better in the sandy loam soil than in the clay loam soil and lasts longer.     

Photocatalytic remediation of γ-hexachlorocyclohexane contaminated soils using TiO2 and montmorillonite composite photocatalyst

TiO2 and montmorillonite composite photocatalysts were prepared and applied in degrading γ-hexachlorocyclohexane(γ-HCH)in soils.After being spiked with γ-HCH,soil samples loaded with the composite photocatalysts were exposed to UV-light irradiation.The results indicated that the photocatalytic activities of the composite photocatalysts varied with the content of TiO2 in the order of 10%＜70%＜50%＜30%.Moreover,the photocatalytic activity of the composite photocatalysts with TiO2 content 30% was higher than that of the pure P25 with the same mass of TiO2.The strong adsorption capacity of the composite photocatalysts and quantum size effect may contribute to its increased photocatalytic activities.In addition,effect of dosage of composite photocatalysts and soil pH on γ-HCH photodegradation was investigated. Pentachlorocyclohexene,trichlorocyclohexene,and dichlorobenzene were detected as photodegradation intermediates,which were gradually degraded with tlle phOtOdegradation evolution.     

Characterisation of Organic Matter and Carbon Cycling in Rehabilitated Lignite-rich Mine Soils

Open-cast lignite mining in the Lusatian mining district resulted in rehabilitated mine soils containing up to four organic matter types: (1) recent plant litter, (2) lignite deposited by mining activity, (3) carbonaceous ash particles deposited during amelioration of the lignite-containing parent substrate and (4) airborne carbonaceous particles deposited during contamination. The influence of lignite-derived carbon types on the organic matter development and their role in the soil carbon cycle was unknown. This paper presents the findings obtained during a six year project concerning the impact of lignite on soil organic matter composition and the biogeochemical functioning of the ecosystem. The organic matter development after rehabilitation was followed in a chronosequence of rehabilitated mine soils afforested in 1966, 1981 and 1987. A differentiation of the organic matter types and an evaluation of their role within the ecosystem was achieved by the use of ¹⁴C activity measurements, ¹³C CPMAS NMR spectroscopy and wet chemical analysis of plant litter compounds. The results showed that the amount and degree of decomposition of the recent organic matter derived from plant material of the 30 year old mine soil was similar to natural uncontaminated forest soil which suggests complete rehabilitation of the ecosystem. The decomposition and humification processes were not influenced by the presence of lignite. On the other hand it was shown that lignite, which was thought to be recalcitrant because of its chemical structure, was part of the carbon cycle in these soils. This demonstrates the need to elucidate further the stabilisation mechanisms of organic matter in soils.     

NATURAL EROSION RATES AND THEIR PREDICTION IN THE IDAHO BATHOLITH1

ABSTRACT: Natural rates of surface erosion on forested granitic soils in central Idaho were measured in 40 m² bordered erosion plots over a period of four years. In addition, we measured a variety of site variables, soil properties, and summer rainstorm intensities in order to relate erosion rates to site attributes. Median winter erosion rates are approximately twice summer period rates, however mean summer rates are nearly twice winter rates because of infrequent high erosion caused by summer rainstorms. Regression equation models and regression tree models were constructed to explore relationships between erosion and factors that control erosion rates. Ground cover is the single factor that has the greatest influence on erosion rates during both summer and winter periods. Rainstorm intensity (erosivity index) strongly influences summer erosion rates, even on soils with high ground cover percentages. Few summer storms were of sufficient duration and intensity to cause rilling on the plots, and the data set was too small to elucidate differences in rill vs. interrill erosion. The regression tree models are relatively less biased than the regression equations developed, and explained 70 and 84 percent of the variability in summer and winter erosion rates, respectively.     

非饱和土边坡稳定的安全分析及进展

笔者基于基质吸力和土抗剪强度之间的关系和非饱和土力学理论 ,以基质吸力问题为中心 ,通过工程实例对影响非饱和土边坡滑动的各种内在及外界因素进行了参数分析 ,尤其对降雨入渗和裂隙影响的定量分析新进展进行了研究。研究结果表明 :非饱和土边坡稳定分析应加强考虑基质吸力对抗剪强度的折减影响 ,修正极限平衡方法对考虑降雨入渗 ,裂隙影响及暂态渗流的非饱和土边坡稳定性研究具有工程意义和实用价值。     

经口摄入土壤多溴联苯醚生物可给性变化及影响因素的体外消化模拟

误食土壤是污染物(如多溴联苯醚)人体(主要是儿童)暴露的重要途径,人体消化道内污染物吸收的生物可给性是针对此种暴露方式进行定量风险评估的有效途径之一.本研究采用体外消化实验模拟3种不同有机碳含量的天然土壤中典型多溴联苯醚(BDE-28、BDE-47、BDE-99和BDE-153)在胃和小肠消化液中的释放,验证部分消化释放的多溴联苯醚因消化残留固相表面的再吸附造成低估实际生物可给性,并通过不同水土比的拟合计算予以校正.结果表明,校正后的消化率普遍高于校正前;就不同土样而言,BDE-28、BDE-47、BDE-99和BDE-153在不同初始暴露浓度条件下平均提升比例范围分别为14.3%~42.3%、11.1%~32.1%、4.9%~12.3%和0.0%~7.7%.因此,未经校正的消化率会显著低估PBDEs消化道内的生物可给性,尤其是低溴代组分及PBDEs初始浓度较高或高TOC含量的土样.校正后BDE-28、BDE-47、BDE-99和BDE-153的消化率分别维持在21.9%~54.7%、18.8%~43.1%、13.4%~27.2%和9.3%~19.9%.此外,PBDEs的消化率与其辛醇-水分配系数的对数lg KOW呈显著负相关;而与土壤TOC含量及PBDEs初始暴露浓度的相关性并不显著,尤其是高溴代组分.