Influence of industry on the geochemical urban environment of Mieres (Spain) and associated health risk

This study is concerned with the elemental composition of soils and street dust collected in an historical industrial city of approximately 27 000 inhabitants, where old Hg mining and metallurgical activities strongly affected the load of heavy metals in the urban environment. For the purpose of the study, representative samples of soils and street dust were collected at different locations in the whole urban area (3 km²). Elevated mean concentrations of As in soils and street dust (69 and 135 g g^–1, respectively), and Hg (3.07 and 4.24 g g^–1, respectively), compared to background levels and to those found in other cities, reflect the anomalous geochemical nature of these materials and the strong influence exerted by the old mining sites.     

改性土壤对模拟含硝基苯废水的吸附

研究了季铵盐阳离子表面活性剂四甲基铵离子（TMA）和十六烷基三甲基铵离子（HDTMA）改性的土壤（黑土、黄棕壤、红壤）对水中硝基苯的吸附作用。结果表明：改性土壤和改性土壤均能吸附水中的硝基苯。但改性土壤对水中硝基苯的吸附能力明显高于未改性土壤。改必土壤吸附硝基苯能力的顺序为1CEC－HDTMA黑土＞1CEC－HDTMA黄棕壤＞0．7 CEC－HDTMA黄棕壤＞1 CEC－HDTMA红壤＞0．7 CEC－HDTMA红壤＞1 CEC－TMA黄棕壤＞1 CEC－TMA红壤。未改性土壤和HDTMA改性土壤对硝基苯的吸附通过分配来进行，吸附等温线可用Henry方程表示，其lgKSOM为2．27，lgKHDTMA为2．87。     

Lead Contamination of Topsoil and Vegetation in the Vicinity of a Battery Factory in Nigeria

Levels of Pb, Zn, Cu, Cr, Ni and Cd were determined in topsoil and vegetation in the vicinity of a factory manufacturing lead- batteries in Ibadan, Nigeria. The samples were collected along five transects in different directions, and varying distances up to 1000m from the factory. Soil lead levels were found to be elevated around the factory, with average levels of about 2000mgkg^–1 close to the fence that declined gradually to about 50mgkg^–1 some 750m away. Soil-lead level around a primary school located about 500m from the factory was as high as 1450mgkg^–1. Lead levels were equally elevated in the vegetation, though average levels in vegetation were slightly lower than in the soil. Cadmium concentrations in soil and vegetation, though low, were more positively correlated with lead levels than any of the other metals are with lead.     

我国桉树人工林立地土壤问题研究概况

我国引种桉树。虽已100多年，但研究桉树人工林土壤问题，却只有50多年的历史。这方面的研究，包括桉树人工林土壤本底调查、土壤性质与林木生长的关系、桉树人工林土壤肥力衰退防治、桉树人工林土壤管理、桉树速生丰产的土壤肥力指标、桉树人工林生态系统土壤养分和水分循环等。文章对这方面研究的概况作了简要的综述。     

广州城郊菜地土壤磷素特征及流失风险分析

通过化学分析和土壤淋洗试验对广州城郊菜地土壤磷素特征和流失风险进行了研究和分析。结果表明.广州城郊菜地土壤全磷含量极高;与自然土壤相比较,菜园土壤无机磷比例增大、有机磷比例降低;无机磷中的AI-P、Fe-P比例增加.O-P比例降低,Ca-P比例基本一致;土壤Olsen P、Bray-1 P、Mehlich-1 P、0.01mol/L CaCl_2和H_2O提取的磷含量相当高;土壤淋洗液中溶解态磷和总磷持续保持很高的浓度,土壤磷供应强度大。菜园土壤中磷进入水体引起水体磷浓度增加,导致水体富营养化风险大;土壤磷的测定值可作为土壤磷流失风险和对水环境影响程度的评估依据。菜地应作为农业非点源磷污染的优先控制区、应通过严格控制磷肥的投入和合理施肥等控制磷的流失。     

2种常规水稻Cd、Zn吸收与器官分配的生育期变化：品种、土壤和Cd处理的影响

Cd在土壤-作物-膳食食物链中的迁移是人类对环境Cd暴露及其健康风险的主要途径,而水稻是子粒Cd积累最强的大宗作物之一.采用全生育期淹水盆栽试验研究了2种常规水稻(高Cd吸收品种“苏香粳1号”和低Cd吸收品种“99-22”)在添加Cd(2mg·kg-1)和不添加Cd处理下对2种土壤(红沙泥田,乌栅土)中Cd、Zn的吸收及其生育期变化.结果表明:1)常规水稻对Cd、Zn的吸收积累受土壤、品种和外源Cd的影响.Cd处理、土壤、品种间的正交互作用(高Cd吸收品种植于高Cd处理且Cd有效性高的红壤中)使常规稻植株Cd/Zn比成数十倍提高,从而使子粒Cd/Zn比产生强烈升高;2)水稻对Cd、Zn的吸收强度因不同生育期而异,Cd吸收的主要时期是分蘖期和成熟期,而Zn吸收的主要时期则是分蘖期、抽穗期和灌浆期.在整个生育期中,水稻Cd吸收伴随着对Zn的排斥现象,这在高Cd吸收下尤为强烈;3)水稻各器官对Cd、Zn的吸收分配无论是同品种的生育期间抑或同生育期时的不同品种间均有显著差异.Cd积累量为根系>穗粒>茎叶,而Zn却表现为茎叶>根系、穗粒.观察到水稻吸收的Cd在生育后期向穗粒的强烈运移.相对于低Cd吸收品种来说,Cd向穗粒转运较强,而Zn的转运较弱是高Cd吸收品种子粒Cd积累强而Cd/Zn比高的植株因素.     

Chemical availability of arsenic and antimony in industrial soils

Total concentrations and extractable fractionations of As and Sb were determined in soil samples from former mining sites in Scotland and Italy. Pseudo-total levels of As and Sb in the sample were between 50–17,428 mg/kg and 10–1,187 mg/kg (Scotland), and 16–691 mg/kg and 1.63–11.44 mg/kg (Italy). Between 0.001–0.63% and <0.001−8.82% of the total soil As and Sb, were extractable using, a single extraction bioavailability estimate. Data from an As-specific extraction procedure revealed that up to 60% of As was associated to amorphous Fe-Al oxyhydroxide phase in all soils. A non-specific-sequential extraction test also showed As to be strongly associated with Fe (and Al) oxyhydroxides at both locations. In the case of Sb, in addition to the crystalline Fe-oxide bound Sb the Al-silicate phase also appeared to be significant. At both sites Sb appears to be chemically more accessible than As with consistent availability despite the varied origin and host soil properties.     

Characterization of dissolved organic matter from saline soils by fluorescence spectroscopy

In this paper hydrophilic (HI) and hydrophobic (HO) fractions of dissolved organic matter (DOM) extracted from soils at different degrees of salinisation were characterised by means of fluorescence spectroscopy in the emission, excitation and synchronous-scan modes. Results provided evidence of the different chemical nature of DOM fractions and allowed to distinguish hydrophilic and hydrophobic fractions extracted from the same soil substrate. The strong decrease in fluorescence intensity observed with the increasing salinity of the soils can be utilised to obtain information on the salinity level of different soil substrates by comparison of spectral fluorescence intensities.     

Analysis of lead in soils adjacent to an interstate highway in Tampa,Florida

In order to assess the amount and distribution of lead pollution in soils adjacent to a major interstate highway serving the city of Tampa, Florida, a total of 224 samples were collected from 32 transects perpendicular to the roadway. The lead content was measured using atomic absorption spectrophotometry. The highest levels of lead were found at distances of 81, 243, and 729 cm from the road. The results show that there is a weak negative correlation between soil lead and the distance from the roadside, as well as with traffic density. The weakness of the relationship is a result of confounding variables such as turbulence and other microclimatic factors, downslope movement of soils overtime, and human action such as construction and highway landscaping. Nevertheless, over one-third of the samples collected in the study area contain more than 500 g g^–1 lead, levels considered to be hazardous by the United States Centers for Disease Control and the Environmental Protection Agency.     

A comparative study of the sorption of O-PAHs and PAHs onto soils to understand their transport in soils and groundwater

Polycyclic aromatic hydrocarbons (PAHs) and their oxygenated derivates (O-PAHs) are identified in soils and groundwater of industrialized sites and contribute to the risk for Humans and the Environment. Nevertheless, data are scarce in literature concerning their retention and transfer in soils and no soil - water partition coefficients are available for these compounds. Sorption of two PAHs, fluorene and acenaphthene and two O-PAHs, 9H-fluorenone and dibenzofuran onto two soils with different organic carbon contents was evaluated and compared by determining their sorption isotherms. Effect of ionic strength and liquid to solid ratio, on fluorene and fluorenone sorption was also evaluated. Sorption equilibrium is achieved within less than 24 hr of mixing and linear sorption models best fit the isotherm data. Acenaphthene and dibenzofuran are similarly sorbed onto the soil. K_D of fluorene is higher than the one of fluorenone, showing a smaller affinity of fluorenone towards the solid phase. This means that O-PAH could form larger contamination plumes in groundwater than PAHs. Decreasing the L/S ratio from 100 to 50 and 30, increases the sorption of fluorenone onto the soil by 56% and 67% respectively, while the sorption of fluorene is slightly increased. Increasing the ionic strength of the aqueous phase also modifies the sorption of fluorenone, contrary to the sorption of fluorene which is slightly affected.