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以泥盆系占优势的南秦岭成矿带中存在有重要的Ｐｂ－Ｚｎ－Ａｇ，Ａｕ，Ｈｇ－Ｓｂ及Ｃｕ矿床。它们形成中晚古生带扬子地块北部被动大陆边缘的沉积盆地演化与造山期中，成矿系列显示出时间与空间的演化特征，构在了一个热水沉积成矿系列，成矿发生于一个热旋回中，各种矿化有相似的物源，每一种地质事件都有特定的金属富集及富集在型和大型矿床是该地区构造－岩浆变质变形作用的最终产物。 相似文献
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应用ＩＣＰ－ＭＳ法测定了岩石中的痕量Ｎｂ、Ｔａ、Ｚｒ、Ｈｆ、Ｔｈ、Ｕ，给出了检出限，并对酸溶和碱熔两种制样方法进行了对比实验。 相似文献
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Marie-PierreAubry WilliamA.Berggren JohnVanCouvering BrianMcGowran BradPillans FritsHilgen 《《幕》》2005,28(2):118-120
The long controversy over the term ‘Quaternary‘ as a chronostratigraphic unit may be reaching an apotheosis, judging from recent papers (Pillans and Naish, 2004; Gibbard et al., 2005; and referencest herein). The debate is no longer centered on whether there should be a place in the geological time scale for a unit termed ‘Quaternary‘-despite its dubious past, it cannot be denied that a large body of earth-historical research is strongly identified with this term. The challenge now concerns an appropriate rank and definition of Quaternary with regard to other chronostratigraphic units. Several options have been proposed (Pillans and Naish, 2004), and Gibbard et al. (2005) encourage a debate on these before decision is reached. In this brief note, we describe an arrangement not previously considered that seems advantageous. It is instructive, however, to first review the Pleistocene Series and Neogene System, the two units that are directly affected by introduction of the Quaternary into the chronostratigraphic hierarchy. 相似文献
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大陆漂移, 板块构造, 地质力学 总被引：2，自引：0，他引：2
本文简要地介绍了魏格纳大陆漂移说的主要内容及其提出的依据; 论述了在大陆漂移说的基础上, 由于海洋地质地球物理调查发现了大洋中脊、洋底扩张, 解释了大陆张裂的机制, 并建立了全球板块构造理论, 形成现代地学思想的革命; 李四光在大陆漂移说提出的同时已在积极地探讨和论述大陆地壳水平运动问题, 并结合中国大陆实际, 发展了陆内碰撞变形理论, 即包括全球大陆构造体系在内的地质力学理论和方法。他强调地质力学是一支脚站在地质上, 另一支脚站在力学上来研究地壳运动和变形现象。后来更扩大了其在资源、环境方面的应用。文章对魏格纳大陆漂移说、全球板块构造理论及地质力学三者的关系做了深入探讨, 论述了李四光地质力学理论方法的现代意义、超前意义, 提出要重视和发扬李四光留给中国人民的宝贵遗产, 建议深入学习李四光的著述, 结合地质调查新成果去丰富它和发展它。 相似文献
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We collected groundwaters in and around a large (313 Mt at 1.08% Cu and 0.3% cutoff) undisturbed porphyry copper deposit (Spence) in the hyperarid Atacama Desert of northern Chile, which is buried beneath 30–180 m of Miocene piedmont gravels. Groundwaters within and down-flow of the Spence deposit have elevated Se (up to 800 μg/l), Re (up to 31 μg/l), Mo (up to 475 μg/l) and As (up to 278 μg/l) concentrations compared to up-flow waters (interpreted to represent regional groundwater flow). In contrast, Cu is only elevated (up to 2036 μg/l) in groundwaters recovered from within the deposit; Cu concentrations are low down gradient of the deposit. The differential behavior of the metals/metalloids occurs because the former group dissolves as anions, enhancing their mobility, whereas the base metals dissolve as cations and are lost from solution most likely through adsorption to clay surface exchange sites and through formation of secondary copper chlorides, carbonates, and oxides. Most groundwaters within and down-flow of the deposit have Eh–pH values around the FeII/FeIII phase boundary, limiting the impact of Fe-oxyhydroxides on oxyanions mobility. Se, Re, Mo, and As are all mobile (with filtered/unfiltered samples ～ 1) to the limit of sampling 2 km down gradient from the deposit. The increase in ore-related metals, metalloids, and sulfate and decrease in sulfate–S isotope ratios (from values similar to regional salars, + 4 to + 8‰ δ34SCDT to lower values closer to hypogene sulfides, + 1 to + 4‰ δ34SCDT) is consistent with active water–rock reactions between saline groundwaters and the Spence deposit. It is likely that hypogene and/or supergene sulfides are being oxidized under the present groundwater conditions and mineral saturation calculations suggest that secondary copper minerals (antlerite, atacamite, malachite) may also be actively forming, suggesting that supergene and exotic copper mineralization is possible even under the present hyperarid climate of the Atacama Desert. 相似文献
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A study was made on samples from one core collected immediately after the December 2004 Asian tsunami to know the geochemical
nature of the offshore tsunami sediments. The core sample was analyzed for sediment grain size, CaCO3, organic carbon (OC) and major elements (SiO2, TiO2, Al2O3, Fe2O3, CaO, MgO, Na2O, K2O, P2O5, MnO). The results indicate that the core sample can be divided into two parts: (1) upper 0–25 cm, interpreted to be deposited
after tsunami (AT), and (2) lower 25–45 cm, interpreted as before tsunami (BT) as evidenced by the sandy nature AT with fluctuating
CaCO3 contents. The AT part is devoid of OC suggesting that the sediment could have been transported to deeper regions along with
the finer particles. Major elements such as SiO2, TiO2, CaO indicate high values than the other elements in AT part than in the BT part. The BT part contains Al rich alluvium mud
associated with finer mud and organic particles. An analysis of the correlation matrix indicates the possible source of elements
and transport of heavy minerals in the AT part than the BT part. The overall results suggest that the sediments could possibly
have two different origins. 相似文献
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Effects of grazing and livestock exclusion on soil physical and chemical properties in desertified sandy grassland,Inner Mongolia,northern China 总被引：3，自引：1，他引：2
Yuqiang Li Halin Zhao Xueyong Zhao Tonghui Zhang Yulin Li Jianyuan Cui 《Environmental Earth Sciences》2011,63(4):771-783
Heavy grazing is recognized as one of the main causes of vegetation and soil degradation and desertification in the semiarid
Horqin sandy grassland of northern China. Soil physical and chemical properties were examined under continuous grazing and
exclusion of livestock for 8 years in a representative desertified sandy grassland. Exclosure increased the mean soil organic
C, total N, fine sand and silt + clay contents, inorganic C (CaCO3), electrical conductivity, and mineral contents (including Al2O3, K2O, Na2O, Fe2O3, CaO, MgO, TiO2, MnO), microelements (Fe, Mn, Zn, B, Cu, Mo), and heavy metals (Pb, Cr, Ni, As, Hg, Cd, Se), and decreased the coarse sand
content, bulk density, and SiO2 in the top 100 cm of the soil. Livestock exclusion also improved available N, P, K, Fe, Mn, and Cu, exchangeable K+, and the cation exchange capacity, but decreased pH, exchangeable Na+, and available S, Zn, and Mo in the top 20 cm of the soil. The greatest change in soil properties was observed in the topsoil.
The results confirm that the desertified grassland is recovering after removal of the livestock disturbance, but that recovery
is a slow process. 相似文献
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R. B. Elliott 《Contributions to Mineralogy and Petrology》1973,38(1):71-79
Sixteen gabbro (hyperite)/amphibolite pairs were collected from geological situations where it seems clear that the amphibolite formed from material similar in composition to that of the adjacent hyperite.Major element analyses show that the hyperite to amphibolite transition was not an isochemical one. K2O, H2O, P2O5 and Fe2O3 were increased strongly. CaO and FeO were diminished; SiO2 may have been also. TiO2, total iron, MgO, MnO and Na2O were static; so probably was Al1O3. 相似文献
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The present study attempted to evaluate the influence of human activity on major elements (Na2O, MgO, Al2O3, SiO2, K2O, CaO, Fe2O3), and to find a method to explore correlations between major elements and human disturbances, according to geospatial theories and methods. The study results indicate that landscapes influence major elements in diverse ways: Al2O3 is closely related to road and mine landscapes; strong relationships exist between MgO, Fe2O3, CaO, and SiO2 and roads; Na2O, SiO2, and Fe2O3 are unrelated to city landscapes; and Na2O is unrelated to road and mine landscapes. 相似文献
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黔北务川瓦厂坪铝土矿床元素迁移规律研究 总被引：6，自引：0，他引：6
黔北务正道地区铝土矿矿床属古风化壳沉积型,成矿母岩具多源性,但主要来源于下覆的中下志留统韩家店组。本文依据Grant提出的质量平衡方程和图解法,对瓦厂坪矿床在成矿过程中元素迁移的富集、贫化（亏损）规律进行了定量研究。结果表明,主要成矿母岩韩家店组砂、页岩一中间产物铝土质页岩、粘土岩是主要元素A12O3、TiO2显著富集... 相似文献
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辽冀地区(主要包括鞍山-本溪地区和冀东地区)位于华北克拉通东北部,产出有诸多BIFs型大型-特大型铁矿床。鞍山-本溪地区和冀东地区是我国最大的两个铁矿集区,其中鞍本地区铁矿储量占全国的24%左右,冀东地区铁矿资源储量占全国的10%以上。虽然辽冀地区BIFs大多为形成于新太古代绿岩带中的Algoma型BIFs,但不同矿区BIFs形成环境和受后期改造的程度不一致,鞍本地区BIFs变质级别为绿片岩相-角闪岩相,冀东地区BIFs经历了绿片岩相-麻粒岩相的变质作用,且辽冀地区普遍发育混合岩化。本文主要对比研究了辽冀地区28个铁矿床200件铁矿石的主量元素特征,为探讨辽冀地区BIFs的形成提供了更多的信息。BIFs样品主要由SiO2和Fe2O3T组成,其中鞍山-本溪地区SiO2+Fe2O3T平均为95.10%,冀东地区SiO2+Fe2O3T平均为88.06%,CaO和MgO含量仅次于SiO2和Fe2O3T,且大部分矿区具有正相关关系,Al2O3、TiO2、K2O、Na2O、MnO、P2O5含量很低,这暗示BIFs原岩为一种化学沉积岩,主要为含有少量碳酸盐泥的硅质和铁质的胶体沉积;辽冀地区Al2O3和TiO2均可见明显的正相关,这可能是由于BIFs沉积过程中有少量碎屑物质的加入,这种相关性在冀东地区更为明显,且除SiO2+Fe2O3T外,其它氧化物含量明显高于鞍本地区,说明冀东地区BIFs形成时沉积环境更为动荡,有更多的碎屑物质加入;虽然辽冀不同地区BIFs经历了不同级别的变质作用,形成了不同的矿物组合,但是氧化物含量却变化不大,这说明了变质反应主要为等化学反应;鞍本地区和冀东地区碱质含量也存在差异性,前者的Na2O和K2O含量均低于后者,且后者Na2OK2O,结合野外地质特征,可能暗示了混合岩化作用对冀东地区的影响更为显著。 相似文献
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The saturation surface of pseudobrookite (Fe2TiO5) was determined for melts in the system SiO2-Al2O3-K2O-FeO-Fe2O3-TiO2 at 1400° C and 1 atm. The variation in concentrations of Fe2O3, TiO2 and Fe2TiO5 in liquids can be used to infer relative changes in activity coefficients of these components with changing K2O/(K2O+Al2O3) of the melts. Saturation concentrations of these components are low and relatively constant in the peraluminous melts and increase with increasing K2O/(K2O+Al2O3) in peralkaline liquids. The activity coefficients of Fe2O3 and TiO2 and Fe2TiO5, therefore, are higher in peraluminous liquids than in peralkaline liquids in this system. In addition, the iron redox ratio was measured as a function of K2O/(K2O+Al2O3) for liquids just below the saturation surface;
was fixed so all variations in redox ratio are entirely due to changes in melt composition. The redox ratio from unsaturated liquids was applied to saturated liquids where redox analysis of the glass is impossible. The homogeneous equilibrium experiments indicate that the activity coefficient of Fe2O3 relative to that of FeO is significantly greater in peraluminous melts than peralkaline melts. Both the heterogeneous and homogeneous equilibria suggest that in peralkaline liquids K+in excess of that required to charge balance tetrahedral Al+3 is used to stabilize both Fe+3 and Ti+4. Calculations show that ferric iron and titanium compete equally effectively for charge-balancing potassium but neither can outcompete aluminum. The observed changes in solution properties of Fe2O3 and TiO2 in the synthetic melts are used to explain variations in Fe-Ti oxide stabilities in natural peraluminous and peralkaline rhyolites and granites. Since the activity coefficients of both ferric iron and titanium are significantly higher in peraluminous liquids than in peralkaline liquids, Fe-Ti oxides should occur earlier in the crystallization sequence in peraluminous rhyolites than in peralkaline rhyolites. In addition, iron will be reduced in peraluminous granites and rhyolites relative to peralkaline ones under comparable P, T, and
. Finally, observed crystallization patterns for minerals containing highly charged cations other than ferric iron and titanium are evaluated in the context of this and other experimental studies. 相似文献
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安徽庐枞盆地酸性蚀变岩帽地质地球化学特征研究 总被引：5，自引：4，他引：1
酸性蚀变岩帽是浅成低温热液系统演化的产物,形成于酸性高氧化性流体的化学条件下;在高硫化型浅成低温热液金矿床中广泛发育,是该类矿床的显著识别特征。通过对酸性蚀变岩帽的野外地质特征、矿物共生组合和地球化学特征研究,能较好阐明浅成低温成矿热液系统的特征、性质、发生和发展演化及成矿作用过程。庐枞矿集区是长江中下游成矿带重要的矿集区之一,盆地内广泛发育以明矾石为特征蚀变矿物的酸性蚀变岩帽,面积超过30km~2,指示盆地内高硫化浅成低温热液系统的存在。目前为止,前期工作主要针对明矾石矿床地质特征和明矾石资源储量进行,该酸性蚀变岩帽的地质地球化学特征研究尚未开展。本次工作通过对酸性蚀变岩帽系统的野外采样、全岩地球化学分析和短波红外光谱测试分析技术(PNIRS测试)分析,确定其主要赋存在砖桥组火山岩中,组成矿物为石英、明矾石、高岭石、地开石,此外有少量绢云母、伊利石、珍珠陶土、叶蜡石、褐铁矿,极少数的叶腊石和黄钾铁矾等,在钻孔深部存在浸染状和半自形粒状黄铁矿。由于受到地表风化剥蚀和不同热热中心的影响,水平方向从矾山明矾石矿床向外围发育石英+明矾石带、石英+高岭石/地开石+明矾石带、石英+高岭石/地开石带、硅化带以及最外围的泥质带即高岭石±绢云母±伊利石带。根据酸性蚀变岩帽的矿物组合和主量元素特征,可将其分为三类:硅质蚀变岩、明矾石蚀变岩和粘土蚀变岩。硅质蚀变岩中SiO_2含量发生明显的富集作用,其余主量元素(K_2O、Na_2O、Al_2O_3、Fe_2O_3、P_2O5)含量显著降低;明矾石蚀变岩和粘土蚀变岩具有相似的地球化学特征,SiO_2、Al_2O_3、Fe_2O_3、P_2O_5元素含量范围变大,K_2O和Na_2O含量降低,且Na_2O降低更加明显;而钛为不活泼元素,在岩石发生蚀变过程中TiO_2含量变化很小。矾山地区的酸性蚀变岩帽的产状、蚀变类型、地球化学特征受构造和地层的双重控制。 相似文献
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The presence in rocks of coexisting sapphirine + quartz has been widely used to diagnose conditions of ultra‐high‐temperature (UHT) metamorphism (>900 °C), an inference based on the restriction of this assemblage to temperatures >980 °C in the conventionally considered FeO–MgO–Al2O3–SiO2 (FMAS) chemical system. With a new thermodynamic model for sapphirine that includes Fe2O3, phase equilibra modelling using thermocalc software has been undertaken in the FeO–MgO–Al2O3–SiO2–O (FMASO) and FeO–MgO–Al2O3–SiO2– TiO2–O (FMASTO) chemical systems. Using a variety of calculated phase diagrams for quartz‐saturated systems, the effects of Fe2O3 and TiO2 on FMAS phase relations are shown to be considerable. Importantly, the stability field of sapphirine + quartz assemblages extends down temperature to 850 °C in oxidized systems and thus out of the UHT range. 相似文献
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The role of phosphorus in rhyolitic liquids as determined from the homogeneous iron redox equilibrium 总被引：1，自引：1，他引：1
The redox ratio of iron is used as an indicator of solution properties of silicate liquids in the system (SiO–Al2O3–K2O–FeO–Fe2O3–P2O5). Glasses containing 80–85 mol% SiO2 with 1 mol% Fe2O3 and compositions covering a range of K2O/Al2O3 were synthesized at 1400°C in air (fixed fO2). Variations in the ratio FeO/FeO1.5 resulting from the addition of P2O5 are used to determine the solution behavior of phosphorus and its interactions with other cations in the silicate melt. In 80 mol% SiO2 peralkaline melts the redox ratio, expressed as FeO/FeO1.5, is unchanged relative to the reference curve with the addition of 3 mol% P2O5. Yet, the iron redox ratio in the 85 mol% SiO2 potassium aluminosilicate melts is decreased relative to phosphorus-free liquids even for small amounts of P2O5 (0.5 mol%). The redox ratio in peraluminous melts is decreased relative to phosphorus- free liquids at P2O5 concentrations of 3 mol%. In peraluminous liquids, complexing of both Fe+3–O–P+5 and Al+3–O–P+5 occur. The activity coefficient of Fe+3 is decreased because more ferric iron can be accommodated than in phosphorus-free liquids. In peralkaline melts, there is no evidence that P+5 is removing K+ from either Al+3 or Fe+3 species. In chargebalanced melts with 3 mol% Fe2O3 and very high P2O5 concentrations, phosphorus removes K+ from K–O–Fe+3 complexes resulting in a redox increase. P2O5 should be accommodated easily in peraluminous rhyolitic liquids and phosphate saturation may be suppressed relative to metaluminous rhyolites. In peralkaline melts, phosphate solubility may increase as a result of phosphorus complexing with alkalis. The complexing stoichiometry may be variable, however, and the relative influence of peralkalinity versus temperature on phosphate solubility in rhyolitic melts deserves greater attention. 相似文献