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浙北平原区土壤硒地球化学研究 总被引：1，自引：1，他引：0
基于嘉善县基本农田质量调查和嘉善县富硒土地资源专项调查中高密度的土壤硒数据及其它测试指标,对浙北嘉善表层土壤硒的含量、分布及影响因素进行了初步研究。分析结果显示,嘉善土壤总量硒平均值为0.33mg/kg,在干窑——姚庄一带存在约57km~2的富硒土壤(Se≥0.40mg/kg);不同土属硒含量差别不大;硒在土壤剖面中分布的总体趋势是硒在表土层聚集;嘉善富硒土壤以有机结合态和腐植酸态两种形态为主,残渣态也占有一定比例。结合全量硒与有机碳的相关性分析和富硒土壤的硒形态分析等结果,本研究认为高硒背景与有机质吸附对嘉善富硒土壤的形成起到了关键作用,改变了嘉善缺硒的认识。 相似文献
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武汉市侏儒-消泗地区农田系统中硒的分布特征及有效性研究 总被引：1，自引：0，他引：1
基于武汉市西南郊蔡甸区2个乡镇土地质量地球化学的调查分析结果,系统总结了区内土壤硒的分布特征,并探讨了有效态硒的影响因素以及硒的生物有效性。研究结果表明,区内土壤表层总量硒平均值为0.379mg/kg,背景值为0.355mg/kg,高于全国背景值,存在富硒地块面积约71.24km2,占调查区总面积的25.30%;土壤有效态硒受土壤全硒、有机碳、CEC、土壤pH值等环境因素的控制;不同农作物的富硒水平不同且与土壤背景值具有一定的相关性。这些研究结果为当地的富硒土壤资源开发利用提供了理论上的支撑。 相似文献
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浙江典型富硒区硒与重金属的形态分析 总被引：7，自引：0，他引：7
通过对浙江西部龙游地区富硒土壤中Hg、Cd、Pb、As等重金属含量的研究表明,成土母岩中与硒伴生的重金属含量较高,由于特殊的地形地貌、母岩风化物质搬运条件以及有利的土壤理化性质等,土壤中重金属大为减少。异常地段重金属形态分析结果表明:土壤中仅有Cd的全量、离子交换态、碳酸盐结合态和弱有机态较高,分别为0.6mg/kg、22.1%、26.5%、11.4%;Se全量平均为0.89 mg/kg,离子交换态、弱有机态含量分别为1.12%、26.4%,碳酸盐结合态仅为0.62%。尽管如此,区内莲子、稻米等农产品仍表现出高硒低重金属等特点,居民健康长寿,发硒含量高,从而为龙游县开发富硒农产品提供了有利条件。 相似文献
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《新疆地质》2021,(2)
通过对焉耆县北大渠乡表层土壤和特色农作物全硒含量测定,分析了研究区表层土壤全硒含量特征及农作物硒含量影响因素。结果表明:表层土壤硒元素含量0.07～1.5 mg/kg,平均0.43 mg/kg,富硒土壤面积105.7 km2,占比88.07%;土壤硒主要以强有机态形式存在,被农作物有效吸收的离子交换态和水溶态硒含量仅占总量的5.94%。不同土壤类型硒平均含量由高到低依次为盐化潮土潮土草甸盐土。相关分析结果表明:土壤TOC和pH值是影响研究区表层土壤硒含量的主要因素,在潮土中二者与土壤硒含量相关性最显著。研究区特色农作物中硒含量不仅受土壤全硒含量影响,且与土壤pH值和土壤TOC密切相关。按相关评价标准,研究区有26件小麦、11件玉米、1件番茄和2件葡萄达到安全富硒食品要求,富硒率分别为78.8%、68.8%、66.7%和33.4%。 相似文献
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北京市平原区土壤中硒的含量和分布 总被引：13，自引：0，他引：13
通过对北京平原土壤硒含量调查和研究,发现北京平原分布有高硒土壤,其特征为沿平原区西部山前断续出现,在北京市区零星分布。表层土壤硒含量为0.04～5.26 mg/kg,平均值为0.20 mg/kg,深层土壤硒含量为0.043～0.22mg/kg,平均值为0.081 mg/kg,总体趋势是硒在表层土壤富集;各类岩石中以炭质页岩中含硒量最高,北京西部富硒炭质页岩的风化可能为平原区土壤硒的来源。相关性分析表明,土壤中Se与有机质呈正相关性,有机质对表层土壤Se具有强烈的吸附与固定作用。 相似文献
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硒是重要的生命元素之一,对动物及人体健康具有重要意义。系统总结了建德市耕地表层土壤硒地球化学特征,分析了土壤硒的分布规律及其与黑色岩系之间的成因联系,探讨了黑色岩系富硒机制,研究了水稻植株中硒富集规律。结果表明,建德市耕地表层土壤硒含量介于0.06~11.5 mg/kg之间,均值为0.35 mg/kg,不同地质背景、成土母质、土壤类型中土壤硒含量差异显著。根据土壤硒和重金属含量,圈出清洁富硒土壤2 647 hm2,主要分布于寒武系灰岩、碳质页岩、钙质泥岩等岩石出露区,指示土壤富硒与这套寒武系“黑色岩系”有密切关系。古沉积学研究认为,黑色岩系形成于缺氧滞水的沉积环境,富含有机质的海底沉积物大量吸附来自地幔的硒,成岩后形成富含硒等元素的黑色岩系。水稻根系土中硒形态组成分析表明,醋酸溶解态硒占比较小,残渣态占比较大,说明水稻根系土中硒可利用性较低。稻米、莲子、草莓及其根系土采样分析表明,稻米对土壤硒的富集系数最高,水稻植株中硒含量具有根>叶>茎≈籽实的特征。 相似文献
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珠江三角洲崖门镇地区水稻田土壤-植物系统中硒元素分布特征及迁移规律研究 总被引：1，自引：0，他引：1
硒在自然环境中的分布及迁移规律一直是研究热点。多目标区域地球化学调查成果表明,珠三角地区土壤硒含量较为丰富,适宜富硒特色农产品种植,但土壤-植物系统中硒的迁移转化规律尚不清楚。本文以典型富硒区—江门市崖门镇为例,系统采集了岩石、风化土、稻田土壤、浅层地下水、灌溉水及水稻样品,应用原子荧光光谱法进行硒含量测试,探讨土壤-植物系统中硒元素分布特征及迁移规律。结果表明:崖门镇花岗岩、花岗岩风化土、稻田表层土壤、剖面土壤、浅层地下水、灌溉水、大米硒含量平均值分别为0.0208mg/kg、0.2325mg/kg、0.5060mg/kg、0.83mg/kg、0.0003mg/L、0.0004mg/L、0.058mg/kg,表层土壤硒含量与珠江三角洲土壤地球化学背景值(0.51mg/kg)相当,大米硒含量达到富硒稻谷标准。土壤-植物系统中硒元素迁移规律为:土壤剖面硒元素向下部迁移,沿径流方向硒向下游迁移。土壤硒较易向水稻根部迁移,较难从根部向水稻地上部分迁移。本研究获得的土壤-植物系统硒元素分布与迁移规律可为该地区富硒资源开发利用提供科学依据。 相似文献
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E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
This paper reports the first results of a study of 11 isotope systems (3He/4He, 40Ar/36Ar, 34S/32S, 65Cu/63Cu, 62Ni/60Ni, 87Sr/86Sr, 143Nd/144Nd, 206–208Pb/204Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others. 相似文献
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奥地利安东帕有限公司 《岩矿测试》2009,28(3):306-306
最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提 相似文献
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S. Viswanathan K. Surya Prakash Rao B. Mahabaleswar 《Journal of the Geological Society of India》2013,82(6):621-627
Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours. 相似文献
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《Applied Geochemistry》2001,16(2):137-159
Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km2 area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population). 相似文献
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《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
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Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations. 相似文献
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S. M. Moosavirad J. Rasouli M. R. Janardhana M. R. Moghadam M. Shankara 《Arabian Journal of Geosciences》2013,6(10):3623-3634
This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds. 相似文献
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Sulfide minerals in the Boulder batholith occur 1. as disseminated grains, visible in hand specimens; 2. in aplitic-pegmatitic pods and masses; 3. along joint and shear surfaces; 4. in hydrothermal veins; and 5. as minute masses within pyrite and silicate minerals and along intergranular sites. Hydrothermally altered rocks have an average sulfide content of 0.8 weight per cent, compared to an average of 0.01 per cent for unaltered rocks. Unaltered rock of the batholith may contain as much as 0.7 weight per cent sulfide. Sulfide inclusions in pyrite, the most abundant sulfide of the batholith, are common and represent a captured iss-phase which later changed to chalcopyrite plus pyrrhotite or mackinawite. Inclusions are most abundant, and more complex, in pyrites of hydrothermally altered and ore rocks. Electron-probe analyses show that pyrites of the Boulder batholith have very similar compositions to those found for pyrites from other ore deposits around the world. 相似文献