湛江市区不同利用类型土壤的PAHs污染特征和来源

多环芳烃(Polycyclic Aromatic Hydrocarbons,简称PAHs)由于具有致癌、致畸、致突变等特性,以及存在较大的健康风险而成为国内外重点研究的污染物之一[1-2]。土壤作为一种重要的环境介质,是PAHs的重要储库和中转站,承担着90%以上的PAHs环境负荷[3]。近年来,我国土壤PAHs     

某氮肥厂场地土壤PAHs污染特征研究

采用现场采样及室内测试方法对广州某氮肥厂原料车间和油库区土壤中16种优控多环芳烃（PAHs）的含量进行调查研究,分析了EPAHs含量及其组成特征和垂直分布特征,并在此基础上进行了源解析。结果表明,分析样品中∑PAHs范围在10-7795μg·kg,原料车间土壤中的∑PAHs小于油库区土壤中的,菲、芘、荧蒽、并（b）荧蒽、苯并（a）芘为主要污染物;油库土壤0-40cm的样品中16种PAHs均有检出,∑PAHs和单体分布基本一致;原料车间土壤∑PAHs和单体浓度随着地面深度的增加而减少。通过对单组分比值（菲／蒽,荧蒽／芘）的分析可以看出油库区土壤中PAHs来源于石油和燃烧源,而原料车间污染源主要为燃烧源。     

北京东南郊再生水灌区土壤PAHs污染特征

采用Eijkelkamp土壤采样器对北京东南郊再生水灌区进行了3个钻孔剖面采样,同时采集了灌溉用水及地下水样品,并采用气相色谱-质谱联用仪对16种多环芳烃（PAHs）进行定量分析。结果表明,表层土壤中有14种PAHs检出,浓度在0.4-53.1 μg·kg-1之间,∑PAHs平均含量为206.7 μg·kg-1,达到了土壤污染临界值;表层以下PAHs的检出种类和含量显著减少,以中、低环的萘、菲、芴、荧蒽、芘为主,∑PAHs仅占表层的3.8%-12.0%,从剖面PAHs含量变化可以判断,低环PAHs较易迁移,迁移性强弱顺序为萘、芴〉菲〉芘、荧蒽;污灌区表土中PAHs组成与大气降尘接近,但与再生灌区有明显差异,这种差异主要由于灌溉用水不同所造成;再生水灌区表土以下土壤剖面检出的PAHs与再生水中的PAHs一致,说明再生水灌溉是导致土壤剖面PAHs污染的主要原因,同时地下水中检出的PAHs种类也与土壤剖面基本一致,但含量较高,可能是早期污水灌溉所造成。     

山东苹果园PAHs污染水平和来源初探

为了探明山东果园土壤中PAHs的污染现状,应用ASE-HPLC技术测试山东红富士主产区果园土壤中PAHs的含量,并对土壤中16种PAHs的分布特征及其生态风险进行探讨。结果表明:15个检测点中有3个检测点存在PAHs污染,含量分别为201.51,833.88,861.28ng/g,说明目前山东苹果园土壤PAHs污染水平较低,生态风险较小,但个别果园已经达到中等污染水平,理论推断会对生态环境产生负面影响。通过分析土壤中PAHs组成可以看出,土样中Ilp/(Ilp+Bgp)值均位于0.20～0.50之间,说明土壤中PAHs主要来源为石化燃烧混合污染,可以作为防止果园土壤PAHs进一步污染的切入点。     

土壤的PAHs污染及其生物治理技术进展

本文阐述了土壤中ＰＡＨｓ的污染来源和荷兰，加拿大等国的ＨＡＨｓ治理标准，分析了影响土壤ＰＡＨｓ生物降解的因素，并对三种好氧生物治理技术进行了评述。     

蚯蚓和发酵牛粪促进南瓜苗修复PAHs污染农田土壤

为了寻求高效修复土壤中持久性有机污染物多环芳烃(PAHs,polycyclic aromatic hydrocarbon),在温室盆栽试验条件下,研究接种蚯蚓和施用发酵牛粪对南瓜苗修复3环以上PAHs污染土壤的影响。试验设置施用牛粪(D)、单接蚯蚓(E)、接种蚯蚓和施用牛粪(ED)、不接种蚯蚓和不施用牛粪的对照(CK)共4个处理,播种10周后收获。研究结果表明,接种蚯蚓和施用牛粪的共同作用下能有效提高南瓜苗生物量,有利于南瓜苗在PAHs污染的土壤生长,特别是地上部分的生长;接种蚯蚓或/和施用牛粪有效地提高了南瓜苗从土壤中吸收3～5环PAHs化合物的效率,且南瓜苗地上部吸收的PAHs量最低是地下部的6倍。因此,结合蚯蚓和发酵牛粪的辅助作用,南瓜苗地上部生物量较大,能从土壤中吸收多种PAHs化合物,与仅依赖于土壤自身的作用相比,三者的共同作用使得土壤中3环以上PAHs化合物的去除率提高23%以上,可组合应用于PAHs污染土壤的强化修复。该研究为土壤多环芳烃污染修复提供参考。     

岩溶区不同土地利用类型土壤无机磷形态分布特征

采用蒋柏藩、顾益初的土壤无机磷分级体系,对桂林毛村岩溶区旱耕地、灌丛、林地、水田土壤的无机磷形态分布特征进行研究。结果表明,岩溶区土壤全磷含量较高,速效磷和无机磷的含量均较低。4种土地利用类型总无机磷含量在49.87～489.80g/kg之间,占全磷的比例在6.08%～56.64%之间。各无机磷形态分布除Fe-P以外,均以水田最高,总无机磷含量水田也为最大。在同一土壤剖面不同发生层次上,Ca2-P、Ca8-P、Al-P、Fe-P、Ca10-P的含量随着深度的增加而减小,O-P含量随着深度增加而升高,对比各无机磷形态含量大小发现:Ca10-PO-PFe-PAl-PCa8-PCa2-P。对各无机磷形态与速效磷相关性分析表明:Ca2-P、Ca8-P、Al-P、O-P与速效磷呈极显著正相关关系;各无机磷形态之间,除Ca2-P与Ca10-P相关性不显著,Ca8-P、Al-P、Fe-P与O-P、Ca10-P相关性不显著,其余各形态无机磷之间均存在极显著的相关性。4种土地利用类型土壤磷素活化系数(PAC)除了水田耕层为2.5%2.0%外,其余土地利用类型的PAC均小于2.0%,说明岩溶区全磷不易转化为速效磷,有效性较低。     

不同类型表面活性剂增效去除焦化厂污染土壤中多环芳烃的研究

Surfactant enhanced remediation is thought to be an effective method for the remediation of soils polluted with hydrophoblc organic compounds. Desorption of polycyclic aromatic hydrocarbons （PAHs） from an abandoned manufactured gas plant （MGP） soil was evaluated using four eluting agents including Triton X-100 （TX100）, sodium dodecylbenzene sulfonate （SDBS）, rhamnolipid water solution （RWS） and rhamnolipid fermentation broth （RFB）. The weight solubilization ratios for acenaphthene and fluorene were in the order of TX100 〉 SDBS 〉 RWS 〉 RFB. The Sm value, which indicates the maximum amounts of surfactants adsorbed in the soil, was in the order of RWS 〉 RFB 〉 SDBS 〉 TX100. By using 8 g L-1 of TX100, SDBS and RWS and 100% of RFB, the T-PAHs removal for the MGP soil contaminated with 207.86 mg T-PAHs kg-1 dry soil was 48.0%, 45.7%, 1.9%, and 8.6%, respectively, while that decreased to 41.6%, 37%, 0.38%, and 1.3% for the soil contaminated with 3494.78 mg T-PAHs kg-1 dry soil. Only 8 g L-1 TX100 could remove all types of the 16 PAHs partly in the MGP soil, and the removal efficiencies of different PAHs ranged from 13% to 77.8%. The results of this study herein provide valuable information for the selection of TX100 surfactant for remediating PAH-contaminated soils in MGP.     

苏南地区农田表层土壤中多环芳烃和酞酸酯的污染特征及来源

采用气相色谱质谱（GC-MS）法测定了苏南地区13个农田表层土壤样品中的多环芳烃（PAHs）和酞酸酯（PAEs）污染物,分析比较了不同区域农田表层土壤,尤其是来自钢铁企业周边的表层土壤中PAHs和PAEs的污染特征及其来源。结果表明,苏南地区农田土壤中总PAHs和总PAEs的浓度分别在147～40300μg·kg-1和0.575～762μg·kg-1之间,其中钢铁厂周边的平均浓度分别为6130μg·kg-1和47.4μg·kg-1。土壤样品中苯并（a）芘的浓度与总PAHs的浓度显著相关,高分子量PAHs在钢铁厂周边表土中含量较高,钢铁冶炼焦化和烧结等工序是其污染来源。酞酸正丁酯（DBP）和酞酸乙基己基酯是苏南地区农田土壤中含量最高的两种PAEs类物质,钢铁厂周边有较高的DBP检出可能与炼钢、冷轧和炼铁等工序有关。本研究将为经济高速发展地区农田土壤环境质量评价、农产品安全生产及土壤污染防治对策的制定提供科学依据。     

产漆酶真菌筛选及其对PAHs污染土壤修复的初步研究

真菌漆酶可以高效转化多环芳烃(PAHs),因此,产漆酶真菌在PAHs污染土壤修复中极具应用前景。根据漆酶可将愈创木酚氧化为红色物质的特性,成功从土壤中筛选出一株能够分泌漆酶的真菌菌株F-1,初步鉴定该菌为疣孢漆斑菌(Myrothecium verrucaria)。通过Plackett-Burman试验对菌株F-1的产酶能力进行了分析,发现特定培养条件组合可将其酶活提高近300倍,达5628 U L-1,表明F-1的漆酶活性受到环境条件的显著影响。应用菌株F-1对PAHs污染土壤进行了初步修复研究,结果表明,接种F-1对菲、荧蒽、芘、苯并(a)蒽、屈、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘、二苯并(a,h)蒽、苯并(g,h,i)苝、茚苯(1,2,3-cd)芘等11种PAHs均有不同程度的降解,提示产漆酶真菌在PAHs污染土壤修复中的应用潜力。     

Kinetics of phosphorus release from calcareous soils under different land use in Iran

The rate of phosporus (P) release from soils can significantly influence P fertility of soils. The objectives of this study were to investigate the effects of land‐use types on the kinetics of P release under different management practices and the relationship between kinetic parameters and soil physical and chemical properties from calcareous soils. The kinetics of P release in 0.01 M CaCl₂ was studied in surface samples of 30 calcareous soils planted to garlic, garden, pasture, potato, vegetables, and wheat. Trend in P‐release kinetics was similar between land‐use types. Significantly different quantities of P were released under different land use. The maximum amount (average of five soils) (46.4 mg kg^–1) of P was released in soil under potato and the minimum amount (10.4 mg kg^–1) under pasture. The kinetics of P release from soils can be described as an initial rapid rate followed by a slower rate. Different models were used to describe P release. In general, parabolic diffusion and power equation were found to be appropriate for modeling P release. The P‐release rate for the soils was estimated by parabolic equation for the studied land‐use types. The constant b was lower for pasture and wheat than for garlic and potato. The relationship between the rate of P release with Olsen‐P was linear, while it was curved with respect to the CaCl₂‐P, indicating that release of P was diffusion‐controlled. When the kinetic parameters of models were regressed on soil properties, CaCl₂‐P and CaCO₃ appeared to be the most important soil properties influencing P‐release rates in these soils.     

Availability of polycyclic aromatic hydrocarbons in aging soils

Purpose  

The soil contamination by hydrophobic organic contaminants (HOCs), such as polycyclic aromatic hydrocarbons (PAHs), poses great threats to human health and ecological security and attracts worldwide concerns. The total HOC concentrations overestimate its available fraction to the soil biota. Increased understanding of the availabilities of PAHs in soil environment will have considerable benefits for their risk assessment and be very instructive to food safety and remediation strategies in contaminated sites. However, the availability of PAHs in aging soils and particularly the correlations of the availabilities with their forms in soils have yet to be elucidated. In this work, the availabilities of PAHs in aging soils were evaluated using a sequential mild extraction technique.     

Physical properties of peat soils under different land use options

Pristine peat soils are characterized by large porosity, low density and large water and organic matter contents. Drainage and management practices change peat properties by oxidation, compaction and mineral matter additions. This study examined differences in physical properties (hydraulic conductivity, water retention curve, bulk density, porosity, von Post degree of decomposition) in soil profiles of two peatland forests, a cultivated peatland, a peat extraction area and two pristine mires originally within the same peatland area. Soil hydraulic conductivity of the drained sites (median hydraulic conductivities: 3.3 × 10^?5 m/s, 2.9 × 10^?8 m/s and 8.5 × 10^?8 m/s for the forests, the cultivated site and the peat extraction area, respectively) was predicted better by land use option than by soil physical parameters. Detailed physical measurements were accompanied by monitoring of the water levels between drains. The model ‘DRAINMOD’ was used to assess the hydrology and the rapid fluctuations seen in groundwater depths. Hydraulic conductivity values needed to match the simulation of observed depth to groundwater data were an order of magnitude greater than those determined in field measurements, suggesting that macropore flow was an important pathway at the study sites. The rapid response of depth to groundwater during rainfall events indicated a small effective porosity and this was supported by the small measured values of drainable porosity. This study highlighted the potential role of land use and macropore flow in controlling water table fluctuation and related processes in peat soils.     

不同栽培方式菜田耕层土壤重金属状况

【目的】评价不同栽培方式(温室、大棚和露地)菜田土壤重金属状况,为菜田土壤质量改善和蔬菜高效安全施肥提供一定的理论依据。【方法】针对我国北方3个区域(东北、黄淮海、西北地区)和南方4个区域(华中、西南、华东、华南地区)主要蔬菜种植区不同栽培方式的典型菜田耕层土壤展开调查,选择的主要菜区不同栽培方式的菜田均为远离城郊的未受到工业“三废”、汽车尾气等污染的农村菜田,取样时间是2013年作物收获后或蔬菜施肥前或生长后期,共采集503个土壤样品,对温室、大棚和露地三种栽培方式下土壤重金属状况进行了研究。【结果】1)采样区设施(温室和大棚)菜田土壤重金属Cu、Zn和Cd总量总体上均高于露地菜田土壤,较露地菜田土壤平均分别高12.2%、21.7%和30.4%。2)随着种菜年限的增加,菜田土壤重金属Cu、Zn和Cd总量呈显著增加的趋势。不同栽培方式菜田土壤中均可能存在几种重金属同时污染的复合污染现象,土壤Cu、Zn、Cd等之间的相关性均达到极显著水平。3)采样区不同栽培方式菜田土壤Cd的二级超标率在19.2%~22.3%之间,温室、大棚和露地菜田土壤Cd的单项污染指数平均分别为0.97、0.98和0.70;土壤Cu、Zn、Pb、Cr、As和Hg的二级超标率在0~14.6%之间,单项污染指数在0.06~0.52之间。【结论】设施菜田N、P2O5和K2O总量及有机肥用量均显著高于露地菜田,可能是造成设施菜田土壤中重金属Cu、Zn和Cd积累显著高于露地菜田的重要原因。采样区设施(温室和大棚)菜田土壤Cd总体上处于污染警戒级状态,露地菜田土壤总体上未受到Cd的污染;设施和露地菜田土壤Cu、Zn、Pb、Cr、As和Hg总体上均未构成对土壤的污染。     

伊金霍洛旗不同土地利用方式下的土壤养分特征

为分析内蒙古鄂尔多斯市伊金霍洛旗在4类土地利用方式(灌木林地、采矿用地、天然牧草地和农地)下,土壤养分质量分数的差异性,运用野外采样和室内化验、分析相结合的方法,测定4种土地类型在0～30 cm土层的土壤有机质和全量氮磷钾质量分数及pH值.结果表明:1)4类土地在0～ 30 cm土层的土壤有机质和全氮质量分数存在显著差异,土壤全磷量和全钾量差异不显著(P＜0.05),土壤有机质质量分数依次为农地＞天然牧草地＞灌木林地＞采矿用地,土壤全量氮磷钾最大值分别为天然牧草地、天然牧草地和灌木林地,最小值分别为采矿用地、灌木林地和天然牧草地;2)在垂直剖面上,采矿用地和天然牧草地的有机质质量分数随着土层深度的增加逐渐减小,农地和灌木林地的有机质质量分数最大值出现在20～30 cm深度的土层,4类土地的土壤全氮量和全磷量均有随土层深度的增加而下降的趋势,全钾量随土层深度的变化不明显.4类土地的土壤全氮和全钾质量分数整体而言较为理想,全磷和有机质质量分数欠缺.农地全磷质量分数基本能满足主要作物的生长需求,有机质和全氮质量分数不能满足主要作物的生长需求.本研究可为内蒙古中部工矿开采区土地合理利用以及退化的生态环境恢复等提供科学依据.     

黄河三角洲不同土地利用类型土壤微观结构特征

黄河三角洲不同土地利用类型盐碱土微观结构的研究,对认识该地区盐碱土的工程性质和对滨海盐碱地治理具有重要意义。该研究结合粒度分析(particle size distribution,PSD)、X射线衍射(X-ray diffraction,XRD)、压汞(mercury intrusion porosimetry,MIP)和扫描电镜(scanning electron microscopy,SEM)方法,对3种不同土地利用类型盐碱土的微观结构进行定量分析,旨在揭示其微观特性,为黄河三角洲盐碱地治理提供微观理论依据。结果表明:不同土地利用类型下的土壤黏粒含量表现大小依次为农田、滩地、草地,而土壤孔隙度大小依次为草地、滩地、农田;农田、草地与滩地盐碱土矿物成分中,石英、方解石和钠长石等原生矿物占绝对优势,仅含少量黏土矿物,且农田黏土矿物含量远大于草地与滩地;草地与滩地盐碱土孔隙特征类似,两者在0.1≤孔隙直径<10μm范围内小孔隙与微孔隙占有绝对优势,而农田盐碱土以孔隙直径在<2μm范围内的微孔隙与超微孔隙为主。农田盐碱土由致密片状、扁平状结构与微裂隙构成,骨架颗粒间由黏土矿物胶结;草地盐碱土由紧密镶嵌的块状颗粒和架空孔隙构成,骨架颗粒间无胶结;滩地盐碱土由紧密堆积的粒状颗粒和粒间孔隙构成,骨架颗粒间无胶结。研究成果可提高对黄河三角洲不同土地利用类型盐碱土微观结构的认识,为滨海盐碱地的治理、利用和开发提供了微观尺度上的依据。     

基于绩效模型的区域土地利用可持续性评价

土地资源可持续利用是社会经济可持续发展的根本保障。该文以土地利用集约度、土地利用程度、土地利用效率和土地利用效益为变量构建了土地利用绩效评价四维模型,并选取23个指标建立了土地利用绩效评价指标体系,根据土地利用变更数据和社会经济统计资料,计算了湛江市1996～2006年的土地利用绩效指数,并依此对湛江市土地利用的可持续性进行了评价。结果表明：湛江市土地利用程度较高但呈总体下降态势,而土地利用的集约度、效率和效益都有明显提高;土地利用绩效总体水平较低但保持稳定增长趋势,指数由1996年的0.3172增长到2006年的0.7163;以1996年为基准年,1997～2006年的土地利用可持续性指数大于0,土地利用处于可持续阶段,说明湛江市的土地利用正逐步优化;土地利用绩效和可持续性的区域分布具有一定的地带性特征。最后,根据土地利用存在的问题提出了土地可持续利用的建议。     

Chemical fractionation of phosphorus in calcareous soils of Hamedan,western Iran under different land use

We investigated the effects of land uses on P distribution and availability in selected calcareous soils under different management practices. KCl‐P (labile P), NaOH‐P (Fe‐Al‐bound P), HCl‐P (Ca‐bound P), and residual P (Res‐P) fractions at 0–30 cm depth were determined for soils planted to garlic, orchard, pasture, potato, leafy vegetables, and wheat. Trends in P distribution between chemical fractions were similar between land uses. Ca‐bound P was the most abundant P fraction in the soils, constituting between 61% and 78% of the total P, whereas P associated with labile was less abundant (< 2%). Soils under leafy vegetables and wheat along with pasture presented the highest and lowest values in all fractions of P, respectively. Labile P generally was highest for leafy vegetables and potato. Labile P and Fe‐Al‐bound P comprised < 1.4% and 8% of total P, respectively. Residual P ranged from ≈ 14% (potato and garlic) to 31% (pasture). Long‐term fertilization increased P allocation to inorganic fractions, as Ca‐bound P contained 78% of total P for potato and garlic and 74% for leafy vegetables but 61% for pasture. A strong positive correlation between labile P and Fe‐Al‐bound P (r = 0.534, p < 0.01), labile P and Ca‐bound P (r = 0.574, p < 0.01), Ca‐bound P and Fe‐Al‐bound P (r = 0.504, p < 0.01), Olsen‐P and CaCl₂‐P (r = 0.821, p < 0.01) was found. Principal‐component analysis showed that the first four components accounted for most of the variation, 32.5%, 16.9%, 12.9%, and 7.9% of total variation, respectively.     

Phytotoxicity of polycyclic aromatic hydrocarbons to willow trees

The toxicity of PAH to willow trees(Salix alba, S. viminalis, S. viminalis x schwerinii) was investigated. Willow cuttings were grown in PH-saturated hydroponic solution (naphthalene NAP, phenanthrene PHEN and benzo(a)pyrene BaP). Toxicity was related to aqueous solubility and was highest for NAP. PHEN did not show significant effects, except in one case. Exposure of trees to BaP showed no effect in two cases, but increased transpiration and growth in two others. High dosages of NAP were fatal for the trees, the lowest dosage significantly stimulated growth. Soil samples were taken from several PAH contaminated sites, among them gas works sites and a former sludge basin. The PAH contents ranged from 1.76 mg/kg to 1451 mg/kg. None of the soils was lethally toxic to the trees, and difference between growth in control soils and growth in PAH contaminated soils was not apparent. Growth and water use efficiency were positively, but not significantly correlated to the PAH content of the soils. Outdoor growth of willows and poplars on the former sludge basin in Valby was monitored, with willows growing faster than poplars(Fopulus trichocarpa). Phytotoxic effects could be observed at some willows at the Valby sludge basin, but it is not sure whether these effects can be contributed to PAH.     

Formation of polycyclic aromatic hydrocarbons in northern and middle taiga soils

An integrated study of the qualitative and quantitative composition of polycyclic aromatic hydrocarbons (PAHs) in the atmospheric precipitation-soil-lysimetric water system was performed using high performance liquid chromatography. It was shown that the accumulation of low-molecular PAHs (phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, and chrysene) in soils is due to the transformation of organic matter and the regional transport and deposition of PAHs with atmospheric precipitation on the underlying surface. High-molecular polyarenes (benz[b]fluoranthene, benz[k]fluoranthene, benz[a]pyrene, dibenz[a,h]anthracene, benzo[ghi]perylene, and indeno[1,2,3-cd]pyrene) mainly result from the decomposition of soil organic matter.