北京市有机氯农药填图与风险评价

采用1个样/km2的密度、1个分析组合样/16km2的方法,对北京市784km2范围内的土壤、大气干湿沉降物、大气颗粒物中HCH、DDT的含量和空间分布特征进行有机氯农药填图.查明2000年北京市地表土壤HCH和DDT的平均含量分别为8.80±11.83ng/g、108.99±301.90ng/g.2006年大气干湿沉降物中HCH和DDT平均含量分别为10.09±9.60ng/g、12.99±13.51ng/g,HCH和DDT的年沉降通量分别为996.57±939.96g/a·km2、1291.53±1342.28g/a·km2.2006年大气颗粒物PM10和PM2.5中的HCH含量分别为0.294±0.205ng/m3和0.217±0.137ng/m3,DDT的平均含量分别为1.037±1.301ng/m3和0.522±0.773ng/m3,显著高于2002-2003年度大气颗粒物中HCH(PM100.01786ng/m3,PM250.01731ng/m3)和DDT(PM100.01672ng/m3,PM2.50.02353ng/m3)的含量,表明北京市或周边地区仍在使用含HCH和DDT化学成分的农药.以2000年北京地表土壤和2006年大气干湿沉降物中HCH和DDT的含量为基础,对2020年土壤中HCH和DDT的时空演变的预测显示,即使干湿沉降物中HCH和DDT的沉降通量每年以5%的速率递减,到2020年土壤中HCH和DDT的环境质量仍不能显著改善,而控制和削减北京及周边地区含HCH和DDT成分农药的使用将是改善北京地表土壤环境质量的关键措施.     

大石围天坑群土壤中有机氯农药的分布与富集特征

选择典型的岩溶地区广西乐业大石围天坑群为研究区,采集不同岩溶地形的土壤,利用 GC-ECD 气相色谱仪测定六六六(HCHs)和滴滴涕(DDTs)两种有机氯农药的浓度.结果表明,大石围天坑群地表土壤、天坑绝壁土壤、天坑底部土壤以及地下河(洞穴)土壤中的 HCHs 和 DDTs 平均浓度分别为0.06 ng/g 和0.02 ng/g、0.31 ng/g 和0.27 ng/g、0.96 ng/g 和0.28 ng/g 以及0.14 ng/g 和0.10 ng/g.研究区土壤中有机氯农药总检出率为:天坑地表<天坑绝壁<天坑底部<地下河(洞穴),随高程降低而增高;有机氯农药(OCPs = HCHs + DDTs)浓度的空间分布特征为:天坑底部>天坑绝壁>地下河(洞穴)>天坑地表,天坑底部 OCPs 浓度明显高于顶部;因此,大石围天坑呈现明显的有机污染物“冷陷阱效应”     

沈阳郊区表层土壤有机氯农药残留特征及风险评价

利用GC-ECD定量测定了沈阳郊区21个表层土壤样品中有机氯农药(OCPs)的含量,并对其残留特征、可能来源及生态风险进行了分析。结果表明,研究区表层土壤中OCPs的检出率达到95.2%,残留量最高值达到111.67 ng·g-1,平均值26.91 ng·g-1,其中以六六六(HCHs)和滴滴涕(DDTs)为主。与国内其他城市土壤中OCPs含量相比,沈阳郊区表层土壤HCHs和DDTs残留属于较低水平,但HCB残留属于较高水平。研究区OCPs的来源解析表明OCPs主要来自环境中的早期残留和近期林丹的使用,六氯苯(HCB)的来源还应包括工业生产。相关性分析说明土壤中总有机碳和水溶盐含量是影响OCPs残留的重要因素。生态风险评价显示表层土壤中DDTs类有机氯农药对该区生物可能仍存在生态风险。     

Sources and transports of organochlorine pesticides in the Nanshan underground river,China

Karst areas have much higher ecological vulnerability and are prone to be contaminated. Organochlorine pesticides (OCPs) were detected in waters and sediment from the two sites of the karst Nanshan underground river system, China, to understand the sources and transport of OCPs in the underground river systems. Obviously, seasonal variations were found both in the waters and the sediments. Detected OCPs ranged from 61 to 936 ng L^?1 in the groundwaters and 51–3,842.0 ng g^?1 in the underground sediments, respectively. OCPs in groundwaters were mixture of younger and older residues from commercial sources. The maximum OCPs in the sediments of the underground river were historically older residues from commercial sources. The sources of OCPs in the waters and sediments of the underground river indicated that the surface systems play an important role in OCPs transport and pollution in the underground river. Karst features were liable for the transport behavior.     

北京郊区地表水中有机氯农药残留水平及特征

有机氯农药滴滴涕(DDT)、六六六(HCH)等化学性质非常稳定,很难生物降解,对环境及人类健康构成了严重威胁。尽管我国从1983年起已禁止使用,但现在的土壤、水等环境样品中仍有不同程度的检出。水资源是自然环境的主要组成要素,又是农业生产的重要自然资源。以往已有学者对北京部分河流地表水中有机氯农药残留进行过研究,发现存在不同程度水体污染。近年来,经过各方大力控制水体污染和环境治理,北京地区地表水中仍有有机氯农药残留,其残留现状是人们十分关心的重要问题。因此本文选择北京郊区为研究区域,采集了温榆河、北运河、延庆、房山、昌平、顺义等地区地表水,分析了水体中DDTs和HCHs污染物的含量以及分布情况,结果表明DDTs、HCHs在北京郊区地表水中均有不同程度的检出,DDTs含量为ND~1398 ng/L,HCHs含量为387~14642 ng/L。本文同时研究了DDT与其代谢产物DDE、DDD的组成比例以及HCH同分异构体的组成特征,对北京郊区地表水中DDTs和HCHs的污染来源进行了简要分析。     

西藏错鄂湖和羊卓雍湖水体及沉积物中有机氯农药的初步研究

对2002年5月采集的西藏错鄂湖和羊卓雍湖的水和沉积物样品进行了实验及分析。结果表明，这2个高原湖泊均不同程度地受到有机氯农药的污染，并具有多种有机氯农药的同时存在、在沉积柱上近表层没有含量下降趋势以及南部的羊卓雍湖污染程度高于藏北的错鄂湖等特点，反映出湖泊中的有机氯农药有可能是随孟加拉湾洋暖流由南向北带人的。两个湖泊的水与沉积物中滴滴涕(DDTs)和六六六(HCHs)含量甚至与我国东部地区的一些淡水水体相近，这种现象很可能表明，大气沉降的有机氯农药可在青藏高原湖泊水体与沉积物中发生一定程度的累积。长远地看，这一过程将可能对青藏高原野生动物产生负面影响。     

Distribution and source of organochlorine pesticides (OCPs) in the sediments of Poyang Lake

The concentrations of typical organochlorine pesticides (OCPs) (DDTs, HCHs, PCP-Na, and HCB) were measured to understand distribution and source of OCPs in surface and columnar sediments of Poyang Lake in 2006. And OCPS concentrations in surface sediment in 2017 were made a comparison with those in 2006 at several same sampling sites. OCPs showed higher concentrations in main stream than in river mouths (entrance of river flow into lake) of the lake. The average concentrations of HCHs and DDTs were 4.63 ± 3.86 and 20.15 ± 26.86 ng/g in surface sediments in 2006, respectively. Concentrations of OCPs in 2017 were lower than in 2006, such as HCHs average 1.98 ± 2.04 ng/g and DDTs average 4.87 ± 1.48 ng/g in 2017, indicating historical residual and degradation. The primary isomers of HCHs and DDTs in the lake were α-HCH, γ-HCH and p,p′-DDD, respectively. HCHs were from historical residual and lindane application. DDTs were from historical residual. PCP-Na total concentrations in surface sediment were 77.36 ng/g in 2006 and 44.04 ng/g in 2017. The concentration of HCB residues in surface sediment was 0.92 ± 0.90 ng/g in 2006 and 0.42 ± 0.38 ng/g in 2017. The concentrations of OCPs in columnar sediments showed annual variations, and the peak concentrations occurred in 1953, 1961, 1974, 1982, and 1995, showing close relations with onset of production OCPs pesticide in 1950s and its later prohibition in 1980s and a large number agricultural cultivated land decrease in 1990s in China. The concentrations of HCB in columnar sediments were average 2.33 ± 1.26 ng/g. OCPs of columnar sediments were from historical residues and lindane input. The main contamination of OCPs was PCP-Na and p,p′-DDD in Poyang Lake. On the whole, the combination of surface samples (0–5 cm in depth) and columnar samples (0–38 cm in depth) in a single study would give insight into OCPs pollution levels in different years (temporal resolution) and in different regions (spatial resolution) in Poyang Lake.     

Microwave-assisted extraction of organochlorine pesticides from sediments and determination by gas chromatograph with electron capture detection

A simple and rapid procedure to extract organochlorine pesticides （OCPs） from sediments by means of microwave energy is proposed. Sediment samples were irradiated with microwaves in a closed vessel system while immersed in hexane-acetone （1 ： 1, v/v）. The sample extracts were cleaned up using solid phase extraction with Florisil as adsorbent. Pesticides were eluted with hexane-ethyl acetate （80 ： 20, v/v） and determined by gas chromatographic separation with electron capture detection. Three oven programs were assayed with two different solvent mixtures in order to achieve adequate experimental conditions for the complete extraction of organochlorine pesticides from the matrix. Different variables such as the composition of extraction solvent,     

Records of organochlorine pesticides in soils and sediments on the southwest of Buenos Aires Province,Argentina

The present study fills a gap in the knowledge in regards to the occurrence of banned pesticides at both coastal and inland locations at the Southwest Buenos Aires region, Argentina. Superficial sediment and soil samples were collected from different sites along the Bahia Blanca Estuary and surrounding sites to assess the concentration levels and spatial distribution of 12 selected organochlorine pesticides (OCs); 13 spatial locations including inland and shore-coast were sampled to evaluate occurrence and concentration levels of hexachlorocyclohexanes α-HCH, β-HCH, δ-HCH, γ-HCH, dichlorodiphenyltrichloroethane and its degradation products (DDXs: p,p′-DDT, o,p′-DDT, p,p′-DDE, o,p′-DDE, p,p′-DDD, o,p′-DDD) and the polychlorobenzenes PeCB (pentachlorobenzene) and HCB (hexachlorobenzene). After cleaning and extractions steps, samples were analyzed by means of gas chromatography/mass spectrometry. ∑OCs (sum of all studied compounds) ranged between 0.206 and 1040 ng g^?1 dw (mean?=?82.4 and SD?=?277 ng g^?1 dw). Total HCHs (sum of α-HCH, β-HCH, γ-HCH and δ-HCH) ranged from 0.0858 to 0.876 ng g^?1 dw (mean?=?0.43 and SD?=?0.23 ng g^?1 dw), DDXs (sum of p,p′and o,p′ isomers) from 0.080 to 1040 ng g^?1 dw (mean?=?81.3 and SD?=?277 ng g^?1 dw). Lower concentrations were found for PeCB (mean?=?0.095 and SD 0.17 ng g^?1 dw) and HCB (mean?=?0.56 and SD 1.7 ng g^?1 dw). Principal component analysis (PCA) permitted the extraction of underlying information about common factors, providing an overview of the distribution of pesticides and allowing the characterization of sites in regards to the major pesticide signature.     

Distribution and potential sources of organochlorine pesticides in the karst soils of a tiankeng in southwest China

This research was conducted in an attempt to assess the concentration levels and potential sources of organochlorine pesticides (OCPs) in the karst soils of Dashiwei tiankeng, southwest China. The tiankeng is a karst surface expression that can act as a focal point for introduction of contaminants to groundwater system, which may serve as condenser and receiver for semi-volatile persistent organic pollutants such as OCPs. In this study, surface soil samples from Dashiwei tiankeng were collected and 23 organochlorine pesticide compounds were analyzed. The results showed that the concentration was 0.019–3.605 ng/g for DDTs (sum of p,p’-DDD, p,p’-DDE, o,p’-DDT, p,p’-DDT), 0.001–0.218 ng/g for HCHs (sum of α-, β-, γ-, δ-HCH), 0.003–0.290 ng/g for CHLs (sum of heptachlor, heptachlor epoxide, TC, CC and trans-nonachlor), 0.001–0.064 ng/g for endosulfan (sum of α-endosulfan and β-endosulfan), 0.008–1.630 ng/g for HCB and 0.023–0.928 ng/g for other OCPs (sum of aldrin, dieldrin, methoxychlor, endrin, endrin aldehyde and endrin ketone). The total OCPs concentrations varied from 0.055 to 5.216 ng/g. The ratio of DDT/(DDE + DDD) in the floor soils of Dashiwei tiankeng ranged from 0.434 to 0.797, suggesting a mostly historical residue of technical DDT contamination. However, the ratio of DDT/(DDE + DDD) in the upper rim soils was higher than one, which that there was fresh DDT application nearby. Both the floor and upper rim soils of Dashiwei tiankeng had high ratios of o,p’-DDT/p,p’-DDT (range of 0.016–10.833 with mean of 5.424 and 4.667–7.714 with mean of 5.723, respectively), which implied that the primary source of DDTs was probably from dicofol-type DDT products. The average ratios of α-/γ-HCH were 24.435 in the floor soils and 1.067 in the upper rim soils, together with the averaged percentages of β-HCH among the total HCH isomers (accounting for 33.772 %), indicating that the HCHs were a dominant contribution from technical HCH usage in the past.     

Occurrence and source identification of organochlorine pesticides in the surrounding surface soils of the Ittehad Chemical Industries Kalashah Kaku,Pakistan

Surface soil and sediment samples were collected from the surroundings of the Ittehad Chemical Industries Kalashah Kaku industrial zone to assess residual level of 19 organochlorine pesticides (OCPs) and identify their sources. DDTs and HCHs were most prevalent OCPs and general pattern of contamination followed the order: ∑DDT > ∑HCH > dicofol > endrin > heptachlor > dieldrin > endosulfan II. Total measured concentrations of HCHs (6.38–121.71 ng/g) and DDTs (759.65–1811.98 ng/g) were greater in the soil samples collected from fodder/rice fields irrigated with the factory effluents and in the surrounding of waste disposal site. Ratios of β to γ-HCH highlighted an old mixed source of technical HCH and lindane in surface soils. Predominance of p,p′-DDT and p,p′-DDE among isomers and metabolites showed that large quantity of technical grade DDT is still present in the surrounding surface soils. Six soil samples were categorized as heavy polluted soils (class III category of DDT > 1,000 ng/g), two soil samples into less polluted soil between class I and II (50–500 ng/g) and 28 soil samples as non-polluted (<50 ng/g) according to environmental quality standards for surface soils. Six soil samples were categorized as less polluted between class I and II of HCHs (50–500 ng/g). Greater concentration of DDTs and HCHs above quality guideline poses potential exposure risk to biological organisms, safety of agricultural products and human health in the surrounding of the Ittehad Chemical Industries.     

鲁西南地区土壤中有机氯农药的残留及其分布特征

在鲁西南地区1.08×104km2的范围内以1点/36km2的采样密度采集表层土壤299件,测试六六六（HCH）、滴滴涕（DDT）等10项指标。研究这些指标的含量变化,发现区内土壤中停用20多年的六六六（HCH）、滴滴涕（DDT）仍有较高的检出率。土壤中六六六（HCH）4种异构体β-HCH含量最高, P,P′-DDE和P,P′-DDD为滴滴涕（DDT）的主要存在形式;进一步研究α-HCH／γ-HCH、β-HCH／γ-HCH和（P,P′-DDE＋P,P′-DDD）/P, P′-DDT值的变化规律,得出调查区内仅滴滴涕（DDT）在局部可能存在新的污染源输入,而大部分地段六六六（HCH）、滴滴涕（DDT）农药使用时间较长,其组分已经通过物理、化学等作用发生了很大变化,污染是过去形成的。土壤环境质量评价结果表明区内土壤质量能保障农业生产、维护人体健康。     

Levels of organochlorine pesticides in natural water along the Yangtze River,from headstream to estuary,and factors determining these levels

Organochlorine pesticides (OCPs), including hexachlorocyclohexane and dichlorodiphenyltrichloroethane, were monitored in 37 samples of water collected along the Yangtze River, the third longest river in the world (6,300 km). The total concentration of OCPs (∑OCPs) in the river water ranged from 0.11 to 27.37 ng/L. It was interesting to discover that, except for some sites near industrial cities, levels of OCPs in the water samples were very similar along the whole river. Significantly, OCPs were detected in Tuotuo River (the origin of Yangtze River) even though OCPs have never been used in this area because of its 4,540 m height above sea level. Furthermore, it was found that ∑OCPs was related to temperature and altitude along the river. We assume OCPs are transported along the Yangtze River, and the factors affecting this process are discussed.     

磁异常解释推断方法探讨及物探应用展望

近几年来,随着战略性矿产远景调查项目的开展,地面高精度磁测一直是主要的物探方法之一,为区域地质调查、成(控)矿地质构造研究、矿产资源评价等工作提供了丰富的地球物理场信息,同时,在金属矿产勘查中能依据矿体与围岩的磁性差异、伴生的磁性矿物直接或间接确定矿体,尤其在铁矿勘查中,磁测更是一种直接找矿的不可或缺的方法。本文总结了磁异常的数据整理及数据处理中一些方法在使用中的问题,并尝试针对解释推断结果提出可靠的、较可靠的、可供参考的三级评价要求。     

中国磁性铁矿石全铁品位和磁性铁品位关系及其意义

中国铁矿以可磁选的低品位磁性铁矿石为主,但是圈定铁矿体多以全铁品位为依据。文章整理了矿产资源储量数据库中磁性铁矿石的全铁品位及其对应磁性铁品位数据,筛选出493组数据,建立了沉积变质型、岩浆型、火山岩型、矽卡岩-热液型铁矿床磁性铁矿石的全铁（TFe）品位与磁性铁（mFe）品位关系式,全部493组数据为mFe(%)=0.9077TFe(%)-3.1442,沉积变质型铁矿为mFe(%)=0.8605TFe(%)-1.8275,火山岩型铁矿为mFe(%)=0.6669TFe(%)+2.6842,矽卡岩-热液型铁矿为mFe(%)=0.9320TFe(%)-3.2442,岩浆型铁矿为mFe(%)=0.8799TFe(%)-3.0174。假定铁矿石的全铁品位为20%和25%时,根据这些关系式估算的磁性铁品位与地质行业规范的边界品位（w(TFe)≥20%,w(mFe)≥15%）和最低工业品位（w(TFe)≥25%,w(mFe)≥20%）十分一致。磁性铁品位的估算,对评价铁矿资源的可利用性、进行国际对比和研究保障程度具有重要参考价值。     

The presentation of an agro-environmental nanocomposite: the study of its acoustic,physical and mechanical properties

Nanocomposites can be used as an acoustic panel to adsorb noise. The aim of this study was to evaluate: (1) acoustic, (2) physical, and (3) mechanical properties of agro-environmental nanocomposites. To prepare the nanocomposites, wood flour, PVA glue, and aluminum nanoparticles (between 1 and 4 %) were hardly mixed and heated at near 220 °C for 120 min. In the next step, sound absorption coefficient, transmission loss, water absorption percentage, thickness swelling percentage, density, flexural strength, flexural modulus, tensile strength, and tensile modulus of nanocomposites were measured. This study showed that the increase in nanoparticle percentage led to the increase in flexural strength, flexural modulus, water absorption percentage, thickness swelling percentage, density, and sound absorption coefficient. But, the increase in nanoparticle percentage led to the decrease in tensile strength, tensile modulus, and transmission loss. The authors think that the nanocomposites are suitable as an agro-industrial nanocomposite to reduce noise.