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11.
A survey was performed to trace the main source of anthropogenic Pb pollution in Mexico City through Pb isotopic signatures (208Pb/204Pb, 206Pb/204Pb, 206Pb/207Pb, and 208Pb/207Pb) from 103 urban topsoil (0–5 cm) samples. Those were collected in the metropolitan area of Mexico City and compared with isotopic compositions of leaded gasoline (LG), domestic Pb ores (DLO) and parent rock (PR). The isotope ratios (IRs) of Pb were determined by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) and total Pb concentration analyzed by wavelength dispersive X-ray fluorescence (WDXRF). The range of Pb concentrations levels in urban topsoil samples was 15–473 mg/kg. The IR values obtained for these samples were 37.965–39.718 (208Pb/204Pb), 18.375–19.204 (206Pb/204Pb), 1.177–1.218 (206Pb/207Pb) and 2.443–2.496 (208Pb/207Pb). Analyzed topsoil samples with low Pb content (<50 mg/kg) displayed high dispersion in 208Pb/204Pb values, which are determined by different natural sources. Samples with 51–200 mg/kg Pb content, shown low dispersion that revealed the mixing between the natural Pb and anthropogenic Pb. The assessment of the IR values shown that, as Pb concentration increases, a trend toward gasoline IR data has been observed. The results obtained by this research suggest that although the use of leaded petrol had been banned in Mexico since 1997, the Pb pollution in the urban topsoils due to the historical use of Pb in petrol is still significant.  相似文献   
12.
An exploratory study has been conducted to test the utility of automated mineral analysis observations to identify flue dust particles in topsoils exposed for several decades to emissions of a copper smelter. The methods used are readily available in mining countries. To identify the most impacted sites, the Cu, Zn, Pb, Mo and As levels in water and diluted sulphuric acid extractions of four topsoil size fractions (833–495 μm, 246–148 μm; 74–38 μm; <38 μm) were analysed. X-ray diffraction analyses were used to demonstrate the mineralogical degradation of smectite phases when approaching the smelter. Flue dust particles in different states of conservation in topsoils were directly observed by scanning electron microscopy (SEM) aided by energy dispersive detection of X-rays. Qemscan® scanning of dispersed topsoil preparations (10,000 particles) pinpoints smelter particles by their density; flue dust pearls can be tracked by sorting particles according to their sphericity, clearly identifying them as pyrometallurgical products. When sorting soil particles by mineral groups (e.g. sulphides), an increase in this phase group can be observed when approaching the smelter. SEM resolution limits observations to particles larger than 2–3 μm. Smaller particles can be observed by transmission electron microscopy, although observer experience and the availability of equipment time are essential as is the case for SEM.  相似文献   
13.
This paper considers the distribution of technogenic 137Cs and naturally occurring radionuclides:238 U,232 Th and40 R concentrations in soils and 137Cs in atmospheric dry depositions by altitudinal belts of the Aragats mountain massif,Republic of Armenia.Undisturbed soil samples were collected at altitudes from 1000 to 3200 m.For the determination of geochemical variability,two soil sampling campaigns were undertaken.Atmospheric dry depositions were sampled from five stations at1100-3200 m collected onto organic fiber filters between June and December 2016.137Cs activity was measured using a high-purity Germanium detector coupled to a multichannel analyzer(Canberra).Results indicated that specific activity of 137Cs in soils at 1000 m is495-528 Bq m^-2,andat3200 mis10,500-11,470 Bq m^-2.No correlation observed for 137Cs versus naturally occurring radionuclides,which varies in distribution by altitude.Specific activities of 137Cs in dry atmospheric depositions varies from 1.06 at 846 m to2.37 Bq m^-2 per quarter at 3200 m and increases as the altitude increases.Activities of 137Cs in soil and dry atmospheric deposition correlated significantly,and 137Cs activity in soils and atmospheric dry depositions decrease as the absolute altitude decreases.The 50-year effective dose from exposure to 137Cs fallout varies with altitude from 0.007 to 1.42 m Sv.  相似文献   
14.
为查明雄安新区西南部耕层土壤的重金属元素污染状况,以唐河-唐河新道、清水河-府河流经区域的农田土壤为研究对象,采用野外采样和室内分析相结合的方法,调查研究耕层(0~20 cm)土壤As、Cu、Zn、Ni、Pb、Cr、Cd和Hg元素的质量分数和分布特征,分析评价重金属元素的污染状况及潜在生态危害风险等级。调查表明,除Cd外,其它重金属元素的平均值均低于土壤风险筛选值,有55%的Cd元素样本超出筛选值,其平均值超出筛选值约26.67%;土壤中As、Cu、Zn、Pb和Cd元素均有不同程度污染,污染程度排序为Cd>Cu>As(Zn)>Pb,其中Cd的污染风险区大面积分布在研究区的中东部,具有典型面状污染特征,Cd元素重度和中度污染的比例分别为3.09%和12.74%;8种重金属元素潜在的生态危害程度排序为Cd>Hg>As>Pb>Cu>Ni>Cr>Zn,其中Cd的生态危害为强、很强和极强的超标率分别为32.43%、31.27%和4.63%;RI值为强生态危害及其以上的比例占38.61%,平均值为287.39。综上表明,雄安新区西南部耕层土壤整体存在重金属元素的污染,重金属的潜在危害程度为中等风险。  相似文献   
15.
通过对高密市耕地表层土壤进行调查,获得了N,P,K,Cu,Zn,Mo,B等7种营养元素全量和有效量,以及pH值和有机质数据,采用数据统计、相关性分析、对比分析等方法,研究有效态地球化学特征及其受控因素。结果表明,元素全量对有效态具有直观制约影响,元素全量与其有效量均呈正相关,与P,K,Cu,Zn有效度呈正相关,表现为协同作用的有N全量对P有效量,P全量对K,Cu,Zn有效量,Cu全量对P,Zn有效量,Zn全量对P,Cu有效量,P全量对K有效量;酸性土壤能够提高N,P,Cu,Zn,Mo元素的生物有效性,碱性土壤能够提高B元素的生物有效性;有机质能够影响土壤营养元素活化,对有效量有一定的促进作用,有机质增加可以不同程度提高K,Zn,B元素的有效度,但会降低N元素的有效度;不同土壤类型的土壤理化性质有所不同,如土壤pH值和有机质的差异,是影响土壤营养元素有效态的重要因素。  相似文献   
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