川西鲜水河断裂带三叠系如年各组放射虫硅质岩的地球化学特征

川西鲜水河断裂带三叠系如年各组放射虫硅质岩的w(SiO2)为71.16%～90.06%,w(Si)/w(Al)为49～71,表明它们含有较高比例的陆源泥质沉积物.硅质岩样品的w(Al2O3)/w(Al2O3 Fe2O3)为0.63～0.81,w(V)＜23×10-6,w(V)/w(Y)<2.8,w(Ti)/w(V)>26, 具有大陆边缘型硅质岩的特征.大部分样品的稀土元素w(Ce)/w(Ce*)为1.02～1.47, w(La)N/w(Ce)N为0.75～1.07, 为大陆边缘型硅质岩,仅一件样品的稀土元素具有大洋盆地硅质岩的特征.对放射虫硅质岩地球化学特征以及浊积岩、玄武岩岩石组合的研究表明鲜水河断裂带在中三叠世拉丁期处于强烈裂陷阶段.     

微波消解-电感耦合等离子体发射光谱法测定固体沥青中微量金属元素

原油、沥青中的微量元素信息已被应用于油气勘探和油气地球化学研究,然而沥青的分析方法较少,而且前处理过程繁琐.本文将微波消解法应用于沥青样品的消解,电感耦合等离子体发射光谱法测定固体沥青中Al、Ca、Fe、K、Mg、Mn、Na、Ti、Ba、Mo、Ni、Sr、V等13种微量金属元素.在高压密闭条件下,微波消解系统消解固体沥青样品的速度快,并确定了样品量和消解条件等影响因素.不同组合消解试剂优化实验研究表明,浓硝酸-氢氟酸作为消解试剂效果最好;通过实验验证在样品处理过程中没有发生损失和污染情况,精密度(RSD,n=8)小于5％,回收率在92.2％～101.0％之间,元素的方法检出限可达0.05 μg/g.本方法为沥青类样品中微量元素分析测定提供了新的参考方法.     

湖北嘉鱼县蛇屋山金矿硅质岩地球化学特征及成矿环境约束

湖北蛇屋山金矿是亚洲最大的红土型金矿,矿区内硅质岩发育,覆于含矿红土层之上,并与硅化灰岩呈渐变过渡。硅质岩主要由微晶和隐晶组成,其SiO2含量为96.87%～97.90%,w(Si)/w(Al)=92.84～287.66,平均值为173,处于纯硅质岩的范畴。硅质岩样品的w(Al)/w(Al+Fe+Mn)为0.189～0.388,平均值为0.303,具热液成因硅质岩的特征。根据Al、Fe、Mn三角图的投点,认为本研究区硅质岩为热液成因硅质岩。微量元素w(Ni)/w(Co)、w(Fe)/w(Ti)、w(Ti)/w(V)、w(U)/w(Th)也说明了硅质岩具有热水沉积成因。w(Ce)/w(Ce*)为1.05～1.27,平均值为1.12,(La/Ce)N为0.84～1.12,平均值为0.98,微量元素V的含量(3.02～4.26μg/g)以及常量元素w(MnO)/w(TiO2)(1.0～2.0)都显示此研究区硅质岩具有大陆边缘硅质岩的特征。结合宏观特征,确定硅质岩有可能形成于卡林型金矿去碳酸盐化阶段,属于热液活动的产物。     

甘肃寨上金矿黄铁矿特征与成因

甘肃寨上金矿是我国重要的卡林型金矿床,发育多种特征的黄铁矿、毒砂、黝铜矿、黄铜矿等金属硫化物。黄铁矿贯穿整个地质过程,对其进行研究可深入理解成矿作用。观察发现,黄铁矿可分为3个世代。第1世代黄铁矿为莓球状黄铁矿(Py1A)和多孔海绵状黄铁矿(Py1B)2类;第2世代中粗粒自形黄铁矿(Py2);第3世代粗粒黄铁矿(Py3)。Py1A呈莓球状,直径介于10～50μm,w(Co)/w(Ni)小于1,w(S+As)/w(Fe)大于2,部分黄铁矿因受到热液改造,莓球中w(Co)/w(Ni)大于1,w(S+As)/w(Fe)小于2;Py1B呈多孔海绵状,w(Co)/w(Ni)大于1,w(S+As)/w(Fe)小于2。Py2呈中粗粒五角十二面体,w(Co)/w(Ni)介于1.41～3.78,w(S+As)/w(Fe)由内向外逐渐升高,介于1.93～2.02,w(Au)/w(As)介于0.023～0.108。Py3呈粗粒立方体晶,周围发育石英压力影,w(Co)/w(Ni)介于1.36～1.39,w(S+As)/w(Fe)介于1.98～2.00。结合地质背景分析认为,黄铁矿微晶直接聚集形成Py1A(莓球状),或在松散状态下经胶结作用形成Py1B(多孔海绵状),并遭受热液叠加改造。Py2(中粗粒五角十二面体)由含矿热液环绕多孔海绵状核部直接结晶形成,Py3(粗粒自形立方体)由晚期热液结晶形成,并同时遭受构造变形活动。该区黄铁矿的特征对于判别地质环境有标型意义。     

白云鄂博群黑色岩系微量元素地球化学特征及地质意义

白云鄂博群位于华北地台北缘,是一套中—新元古代裂谷沉积的产物。尖山组和比鲁特组是其中主要的黑色岩系。对以上两组中的碳质页岩和板岩的Au、Ag、As、Ba、Co、Cu、Hg、Mn、Mo、Ni、P、Pb、V、Zn、U、B、Sb等微量元素和稀土元素进行了较为详细的研究。通过元素含量特征、w(V)/w(V+Ni)、w(Zn)-w(Co)-w(Ni)三元图、稀土配分曲线、w(Ce)/w(La)、Ce和Eu异常、w(La)/w(Yb)-w(Ce)/w(La)和w(La)/w(Yb)-w(ΣREE)图解等方法对其沉积环境特征进行了探讨。微量元素含量分析显示白云鄂博群黑色岩系以富亲铜元素和亲石元素、贫亲铁元素为特征,其中富集Hg、B、As、Mn、Sb、Au、Ag、Pb、P、Ba、U、Mo等多种元素;较高的w(B)反映了黑色岩系沉积于盐度较高的水体中;高的w(V)/w(V+Ni)、w(Ce)/w(La)反映了黑色岩系形成于缺氧的沉积环境中;黑色岩系中Hg、Sb、Ba的富集和w(Zn)-w(Co)-w(Ni)图解中投点大部分靠近热水沉积区域指示了黑色岩系中有热水沉积物的参与;稀土元素配分模式、Ce和Eu异常及w(La)/w(Yb)-w(ΣREE)和w(La)/w(Yb)-w(Ce)/w(La)图解投点在两岩组中的不同特点表明尖山组沉积物以陆源沉积为主,有少量热水沉积物参与;而比鲁特组中热水沉积组分所占比例较大,形成时海水较深。     

河北平泉中元古代高于庄组和杨庄组地球化学特征

根据河北平泉地区中元古代高于庄组和杨庄组中21件岩石样品分析结果,显示常量元素和微量元素的含量在纵向上的演变规律不明显,但各种元素含量在岩石地层界线均有明显变化,表明地球化学特征可作为划分沉积地层的标志或对已划分的地层界线进行优化.此外,据w(CaO)/w(MgO)值、w(Ca)/w(Ca Fe)值、w(Sr)/w(Ba)值及V、Pb、Co、Ni和Ti等元素特征分析,高于庄组与杨庄组的沉积环境有极大的差异.高于庄组为远岸深水海洋环境下的沉积,陆源碎屑供应匮乏;而杨庄组为干热气候下的近岸海洋环境沉积,具有较多的陆源碎屑物质供应.     

微量元素在油气化探中的应用

无机组分虽然不是油气的基本组分,但它们种类繁多,与油气烃类的生成运移有着不可分割的联系。因此针对与油气田伴生的微量元素进行分析研究并寻找油气是一种有效的地球化学勘查方法。通过研究发现:油气评价的有效微量元素指标主要为Hg和w(V)/w(Ni)、w(V)/w(Fe),其次为w(N)/w(Org.C)、Pb、U;微量元素油气化探异常模式为环状,即油气藏上方为低值区,油气藏边缘为高值异常区。     

微波消解-高分辨电感耦合等离子体质谱法测定土壤中8种金属元素

微波消解结合电感耦合等离子体质谱(ICP-MS)是土壤样品中金属元素测定的常用方法,其前处理可以采用不同的消解体系,但是消解体系对分析结果的准确性影响较大。此外,应用ICP-MS测定某些元素时干扰的存在会影响结果的准确性。基于上述问题,本文优选三个酸体系微波消解溶样,采用高分辨电感耦合等离子体质谱(HR-ICP-MS)测定土壤样品中8种金属元素(Cr、Co、Ni、Cu、Zn、Pb、Cd和U)的含量,对比研究了由不同用量硝酸、盐酸、氢氟酸混合组成的三个酸消解体系对国家土壤标准物质的消解效果,确定了最优前处理方法。结果表明：经国家土壤标准物质验证,采用HR-ICP-MS检测,在不需要干扰校正的情况下,酸体系Ⅰ(6mL硝酸+3mL盐酸+3mL氢氟酸)和酸体系Ⅱ(2mL硝酸+6mL盐酸+1mL氢氟酸)的测定值与标准值相吻合,方法检出限为0.001～0.715μg/g,精密度(RSD,n=6)小于7.0%。从消解情况、准确度和精密度比较,酸体系Ⅰ稍优于酸体系Ⅱ;从酸用量比较,酸体系Ⅱ酸用量最少。两种酸体系的样品处理方法均具有较高的适用性和可靠性,都可用于土壤样品中8种金属元素含量的直接测定。     

碰撞/反应池ICP-MS测定煤及燃煤产物中V、Cr、Co、Ni、Mn五种过渡金属元素

<正>近年来,煤以及燃煤产物中过渡金属元素的研究越来越备受关注,这主要是因为过渡金属元素在国防事业和航空事业中的应用越来越广泛。本文采用微波消解电感耦合等离子体质谱法(ICP-MS),应用碰撞反应池(CCT)模式测定了煤及燃煤产物(飞灰)中的V、Cr、Co、Ni、Mn五种过渡金属元素;建立了测定煤及燃煤产物中V、Cr、Co、Ni、Mn过渡金属元素的方法。在测试过程中采用Rh作为内标,通过     

微波消解电感耦合等离子体质谱法测定地球化学样品中钒铬镍锗砷

地质样品中多种元素的分析,通常采用高压密封消解电感耦合等离子体质谱法(ICP-MS),而应用于测定地球化学样品中的V、Cr、Ni、Ge、As等元素,影响分析准确度的主要原因有:样品前处理方面,高压密封罐会释放Cr和Ni污染样品,同时Ge和As属于易挥发元素容易造成损失;质谱测定方面,多原子分子离子会产生干扰。本文针对两方面的干扰因素,对比了微波消解硝酸提取、微波消解王水提取、高压密封硝酸复溶、高压密封王水复溶四种前处理方法中待测元素的溶出效果以及污染或损失情况。结果表明,采用微波消解替代高压密封罐消解可消除引入的Cr、Ni污染,避免了Ge、As挥发损失,同时微波消解的时间短。而采用硝酸提取,由于避免了氯的引入,分析效果优于王水提取。且使用八极杆ICP-MS氦气碰撞模式消除了样品基体中的氯多原子分子离子干扰(如37Cl14N对51V干扰,35Cl16OH对52Cr干扰,35Cl37Cl对72Ge干扰以及40Ar35Cl对75As干扰等)。应用微波消解硝酸提取、ICP-MS测定岩石、水系沉积物和土壤国家标准物质,V、Cr、Ni、Ge、As的检出限分别为1.09、0.19、0.55、0.02、0.50μg/g,精密度(RSD)4%,而采用高压密封消解、ICPMS测定V、Cr、Ni的检出限为3.48、13.09、21.67μg/g(Ge和As由于挥发无法用此法检测)。运用微波消解硝酸提取-ICP-MS氦气碰撞模式测定地球化学样品中V、Cr、Ni、Ge、As,简化了分析流程,样品消解时间仅2 h,相比于高压密封方法(消解时间48 h)具有消解快速、多元素同时测定、检出限低的特点。     

塔里木盆地寒武系原油微量元素特征及意义

塔里木盆地是中国最大的内陆含油气盆地,有关盆地内主力烃源岩层位时代目前仍存在一定争议。油-油对比能够 发现原油间的亲缘关系,明确不同类型原油地球化学特征,是解决这一问题的有效手段。中深1井及中深1C井发现的中寒 武统阿瓦塔格组、下寒武统肖尔布拉克组原油可以作为重要的端元油类型参与油-油对比。本文通过对比两种寒武系原油 及盆地内多种轻质原油微量元素组成,发现根据多种过渡金属元素比值进行聚类分析可将盆地内轻质原油分为I类和II类, Cr/V,Ni/Mn,Ni/Mo比值是原油分类的良好指标。I类原油较II类原油具有较低的Cr/V比及较高的Ni/Mn与Ni/Mo比,表明 其烃源岩沉积环境相对还原。本次分类结果与前人有机地球化学研究相符,表明无机地球化学指标可作为原油分类的重要 参考,具有较大的应用潜力。     

江汉油田原油和生油岩有机抽提物中过渡族微量元素特征及其石油地球化学意义

运用中子活化分析方法对江汉油田原油和生油岩有机抽提物中过渡族微量元素Sc、V、CrMn、Fe、Co、Ni、Zn等进行了重点研究,测定了这些元素的丰度值。研究了这些元素在原油和有机抽提物族组份:沥表质、非烃和芳香烃中的变化规律。在此基础上,讨论了这些微量元素的相关性,并运用它们的丰度比值对数分布和归一化对数分布,进行了油-源对比的尝试。     

Elemental characteristics and paleoenvironment reconstruction: a case study of the Triassic lacustrine Zhangjiatan oil shale,southern Ordos Basin,China

Using trace elements to reconstruct paleoenvironment is a current hot topic in geochemistry. Through analytical tests of oil yield, ash yield, calorific value, total sulfur, major elements, trace elements, and X-ray diffraction, the quality, mineral content, occurrence mode of elements, and paleoenvironment of the Zhangjiatan oil shale of the Triassic Yanchang Formation in the southern Ordos Basin were studied. The analyses revealed relatively high oil yield (average 6.63%) and medium quality. The mineral content in the oil shale was mainly clay minerals, quartz, feldspar, and pyrite; an illite–smectite mixed layer comprised the major proportion of clay minerals. Compared with marine oil shale in China, the Zhangjiatan oil shale had higher contents of quartz, feldspar, and clay minerals, and lower calcite content. Silica was mainly in quartz and Fe was associated with organic matter, which is different from marine oil shale. The form of calcium varied. Cluster analyses indicated that Fe, Cu, U, V, Zn, As, Cs, Cd, Mo, Ga, Pb, Co, Ni, Cr, Sc, P, and Mn are associated with organic matter while Ca, Na, Sr, Ba, Si, Zr, K, Al, B, Mg, and Ti are mostly terrigenous. Sr/Cu, Ba/Al, V/(V + Ni), U/Th, AU, and δU of oil shale samples suggest the paleoclimate was warm and humid, paleoproductivity of the lake was relatively high during deposition of the shale—which mainly occurred in fresh water—and the paleo-redox condition was dominated by reducing conditions. Fe/Ti ratios of the oil shale samples suggest clear hydrothermal influence in the eastern portion of the study area and less conspicuous hydrothermal influence in the western portion.     

Assessment of contaminants in Dubai coastal region, United Arab Emirates

Coastal uses and other human activities have inevitably impinged on the Gulf environment; therefore, these regions require continuous monitoring. The investigated area covered the maximum fragments of Dubai coastal region in the Arabian Gulf. The determination of major oxides and trace metal concentrations in Dubai sediments revealed three heavily and moderately contaminated regions. One is in the far northeastern part at Al-Hamriya Sts 1–3 and contaminated by Fe, Cu, Pb, and Zn; the second is in the mid-northeastern part at Dry Docks and contaminated by Cu, Ni, Pb, and Zn; and finally, the third is in the near southwestern part at Dubal and contaminated by Fe, Mg, Cr, Ni, and Zn. Al-Hamriya St 3 represented the highest values of Cu, Pb, and Zn, whereas Dubal exhibited the maximum values of Fe, Mg, Ba, Cr, Mn, Ni, and V. The anthropogenic discharge and natural deposits are the main sources of contamination. In general, all trace and major elements showed the minimal levels at Jebel Ali Sanctuary (Sts 11, 12, 13) except for Sr and Ca, which showed their maximum values. The highest concentrations of Ca and Sr are mainly attributed to carbonate gravel sands and sands, which cover most stations. Each of V and Ni showed negative correlation with TPH, which may be indicated that the source of oil contamination in the region is not related to crude oil but mostly attributable to anthropogenic sources. The significant positive correlation, which was found between trace metals and TOC indicates that organic matter plays an important role in the accumulation of trace metals in case of Cu, Zn, and Pb.     

Geochemical characteristics and analysis of crude-oil source in the deep-water area of the Baiyun Sag,South China Sea

In the Baiyun Sag, the oil relationship with possible source rocks is complicated, and little research on oil sources in the area has been performed. In this paper, geochemical studies of carbon isotopes, biomarkers, paleoenvironmental deposition, and crude oil maturity, carried out with the use of oil samples from the Baiyun Sag, demonstrate that the organic matter in crude oil has an oxidizing depositional environment and primarily lacustrine facies conditions, with a significantly higher plant input. The oil samples used are mature to highly mature. Crude oil in the northern area of the Baiyun Sag is more mature than samples in the eastern part of the sag. Despite limited source rock data, we were able to conclude that the crude oil samples were derived mainly from the Enping Formation; other potential source rocks of the Wenchang and Zhuhai Formations may also have contributed to the reservoirs in different parts of the sag. Furthermore, the source of crude oil in each structure in the Baiyun Sag was analyzed; for example, crude oil in the LH19-5 structure was generated from the organic matter of the Enping Formation, and crude oil in the LW3-1 structure was derived from the mixed organic matter of the Enping, Wenchang, and Zhuhai Formations. © 2018, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved.     

准噶尔盆地东南缘芦草沟组油页岩元素地球化学特征及沉积环境指示意义

本文通过XRF和ICP-MS测试方法对油页岩样品进行测试,根据常量元素和微量元素特征、组分含量及某些元素的比值,探讨了研究区油页岩样品的地球化学特征,进一步阐述了其沉积环境的指示意义.结果表明,P和B元素强烈富集,相当硼及古盐度值都表明属于半咸水沉积环境,B/Ga、Sr/Ba值也说明受到海水影响或间歇性受海水影响,沉积环境以半咸水湖泊为主;Fe2+/Fe3+、V/(V+Ni)、V/Ni、Cu/Zn、Ni/Co和U/Th值及Ni的含量说明沉积环境为咸化的弱还原—还原环境;Mn/Fe和Mn/Ti值也较小,反映近岸的沉积环境;Sr/Cu表明主力油页岩形成时期处于温湿—干热气候.总体上反映出,研究区油页岩的沉积介质环境的显著特征是半咸水状态的弱还原—还原环境.     

Geochemistry,Paleoenvironment and Mechanism of Organic-Matter Enrichment in the Lower Silurian Longmaxi Formation Shale in the Sichuan Basin,China

To investigate the mechanism of the organic-matter enrichment in the Lower Longmaxi Formation shale, the geochemistry and total organic carbon(TOC) of the Longmaxi Formation black shales in the Jiaoshiba, Zhaotong, and Weiyuan areas of the Sichuan Basin were analyzed. Paleoproductivity proxy parameters(Babio, Siex, and Ni/Al), clastic influx proxies(TiO_2 and Ti/Al), redox indices(V/Cr, Ni/Co, V/(V+Ni), and U/Th), and hydrothermal indicators(Fe, Mn,and Y concentrations; Fe/Ti ratio and a Ni-Zn-Co diagram) were employed to decipher the paleoenvironment of the Lower Longmaxi Formation shales. TiO_2 and Ti/Al indicated low terrigenous detrital influx in all three areas. However, Babio, Siex,and Ni/Al indicated high productivity in the Jiaoshiba area. V/Cr, Ni/Co, and U/Th indicated higher oxygen content with larger fluctuations in the Zhaotong and Weiyuan areas. Fe, Mn, and Y concentrations and the Fe/Ti ratio implied greater active hydrothermal activity in the Weiyuan area. These heterogeneities were considered to be closely related to the paleoenvironment and paleogeography, and the large basement faults that developed during the Chuanzhong paleo-uplift could have provided vents for deep-hydrothermal-fluid upwelling. The redox indices(V/Cr, Ni/Co, and U/Th) and a paleoproductivity proxy(Ni/Al) displayed a significant correlation with the TOC, suggesting that both excellent preservation conditions and high paleoproductivity were the controlling factors for the enrichment of organic matter in the Longmaxi Formation shale. There was no obvious correlation between the clastic influx proxy(Ti/Al) and the TOC due to the extremely low supply of terrigenous debris. The hydrothermal indicator(Fe/Ti) was negatively correlated with the TOC in the Weiyuan area, indicating that hydrothermal activity may have played a negative role in the accumulation of organic matter. This study suggests that the enrichment of organic matter in the Longmaxi Formation marine shale varied according to the paleogeography and sedimentary environment.     

Trace element characterisation of Cretaceous Orange Basin hydrocarbon source rocks

Trace elements in the kerogen fraction of hydrocarbon source rock samples from two wells obtained from the Cretaceous units of the Orange Basin, South Africa were determined using X-ray fluorescence spectrometry, in order to determine their distribution and geochemical significances. The concentrations of the elements (As, Ce, Co, Cu, Fe, Mo, Ni, Pb and V) determined ranged from 0.64 to 47,300 ppm for the samples analysed. The total organic carbon (TOC) values indicate that the samples are organic rich but did not show any trend with the distribution of the trace metals except Ce, Mo and Pb. Dendrogram cluster analysis discriminated the samples into three groups on the basis of their level of thermal maturity. Thermal maturity has a significant effect on the distribution of the trace metals. Cobalt/Ni and V/Ni ratios and cross plots of the absolute values of V and Ni indicate that the samples had significant marine organic matter input. The V and Ni contents and V/(V + Ni) ratio indicate that the organic matter of the source rocks had been deposited in reducing conditions. Despite the similarities in the organic matter source input and depositional environment of the organic matter of the samples from the two well, cross plots of Co/Ni versus V/Ni and Mo/Ni versus Co/Ni were able to reveal subtle differences. Cluster analysis of the samples was also able to reveal the subtle thermal maturity differences of the samples.     

微波消解-电感耦合等离子体质谱法测定植物样品中微量元素

采用过氧化氢-硝酸作溶剂,微波消解样品,外标方法校准,电感耦合等离子体质谱法同时测定植物样品中硼、镉、铜、钴、铬、钼、锂、镍、铅、镧、锗11个微量元素。确定了微波消解仪和等离子体质谱仪的最佳工作参数,研究了有机残留物和共存离子的干扰和消除方法,选择了各元素的测定同位素,以45Sc和103Rh双内标补偿基体效应,建立了样品测定方法。方法检出限(10s)在5~150 ng/g,相对标准偏差(RSD,n=12)在1.27%~5.27%。对多种国家一级生物标准物质进行分析验证,测定值与标准值相符。方法适用于植物的果实、根、茎、叶等不同类型样品中多种微量元素的测定。     

贵州遵义中南村黑色岩系黄铁矿的成分标型与成因探讨

对贵州遵义中南村黑色岩系多元素矿床黄铁矿中的Co、Ni、As、Se、Te、n(s)／n(Fe)、w(Co)／w(Ni)、w(S)／w(Se)、w(Se)／w(Te)等标型进行了研究,井将其与4个胶东热液型金矿的黄铁矿的相应数据进行了对比。通过成分标型分析,并结合黄铁矿的形态、内部结构和同位素特征以及前人的研究成果．认为此黑色岩系多元素矿床应为海底热水沉积和生物沉积混合成因。该黑色岩系黄铁矿同胶东界河金矿的黄铁矿、胶东金青顶金矿中的黄铁矿、胶东玲珑金矿西山矿区中的黄铁矿和胶东三山岛金矿床中的黄铁矿等热液金矿型黄铁矿在10000×w(Co+Ni)／w(Fe)-10000×w(As十Se十Te)／w(S)-100×(n(S)／n(Fe)-1.8)三角图上的投点明显不同,前者投点甚为分散,后者投点较集中。从成因角度分析认为：后者的物质来自花岗岩,主成矿过程受单一的温度变化范围不大的岩浆热液控制;前者物质来源复杂,受高温阶段的深部循环热水和低温阶段的海水一热水混合流体甚至生物作用的制约。由此可以初步提出以下一般判据：在10000×w(Co十Ni)／w(Fe)一10000×w(As十Se+Te)／w(S)一100x(n(S)／n(Fe)一1.8)三角图上,成因简单的黄铁矿的投点较集中,成因复杂的黄铁矿的投点较分散。