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1.
自生菱铁矿很好地记录了其形成时的地质信息及海洋中的生物地球化学过程，是示踪成岩作用带和氧化还原环境变化的绝佳载体。台湾国姓地区中新世猴洞坑组海相泥页岩中发育有大量自生菱铁矿结核，是次氧化带的产物。为进一步确认该菱铁矿形成时所处沉积环境的氧化还原状态和生物地球化学过程。本文对该区菱铁矿中保存完好的草莓状黄铁矿开展了粒径和硫同位素研究。结果显示，草莓状黄铁矿的粒径变化较大，平均粒径为9.23～11.55μm,最大粒径大于20μm,显示氧化-弱氧化的沉积环境特征；黄铁矿的δ34S为-28.5‰～+3.1‰,平均值为-11.7‰,相较于海水(+21‰)富集轻的硫同位素，表明黄铁矿形成于相对开放的浅表层沉积物。黄铁矿的粒径分布规律和硫同位素特征均指示台湾国姓地区中新世海相菱铁矿形成于浅层弱氧化的次氧化带内。  相似文献   

2.
扬子克拉通秭归地区震旦系陡山沱组第四段黑色泥页岩中广泛发育具明显δ13C负异常的碳酸盐岩结核,其是否与古甲烷天然气水合物渗漏有关值得深入研究.对该碳酸盐岩结核开展的沉积结构构造、岩相学和地球化学研究表明,碳酸盐岩结核具典型韵律环带结构,普遍发育有亮晶球体结构、草莓状黄铁矿,以及与渗漏系统有关的凝块组构,δ13C具明显负异常(-5.65‰~-6.76‰),U、Mo元素强烈富集(UEF=8~26,MoEF=99~320),Y/Ho比值为31.05~37.31,稀土配分型式为平缓左倾,主微量元素K、Sc、V、Cr、Co、Ni、Rb、Sr、Ba、Th、U和Mo等总体显示为缺氧-硫化环境,与冷泉碳酸盐岩的形成环境和特征一致.碳酸盐岩结核环带SiO2、MgO、CaO、CO2等地球化学元素含量呈阶段性连续增减变化,显示碳酸盐岩结核形成经历了初始形成、成岩-交代、成岩后改造3个连续演化阶段.据此,提出碳酸盐岩结核是新元古代末噶斯奇厄斯冰期(582~551 Ma)结束温度回暖,黑色泥页岩中低温封存固态天然气水合物发生分解释放和成岩-交代形成的冷泉碳酸盐岩结核,也是古天然气水合物存在的重要地质记录和标志,这一新认识为华南扬子克拉通在震旦系和下古生界沉积盖层中寻找页岩气(甲烷天然气)储集层位提供了重要地质依据.   相似文献   

3.
“大塘坡式”锰矿在我国华南黔湘渝地区广泛分布, 是我国最重要的锰矿资源类型之一。它的形成与新元古代Sturtian雪球事件密切相关, 但其具体的成矿机制尚不十分清楚, 还存在许多争论。本文对贵州铜仁地区新近发现的高地超大型锰矿和共伴生黑色页岩中的微量硫酸盐和黄铁矿的硫同位素、菱锰矿等碳酸盐岩及有机碳的碳同位素进行了系统研究, 对该类型锰矿的成矿环境和沉淀机制进行了探讨。高地锰矿大塘坡组一段含锰黑色页岩和锰矿石中硫酸盐的含量很低, 为30.9 ~ 20 439.7 μg/g, 平均3 322.5 μg/g, 硫酸盐的δ34SVCDT为51.5‰~68.1‰, 平均60.4‰。冰碛岩上部铁丝坳组含砾杂砂岩中黄铁矿的δ34SVCDT为26.8‰~59.6‰, 平均52.1‰; 上覆大塘坡组黑色页岩和锰矿石中黄铁矿的δ34SVCDT为53.7‰~65.6‰, 平均63.3‰, 与前人在该区域其它矿区得到的结果一致, 与硫酸盐的δ34SVCDT值差别不大; 黑色页岩和锰矿石全岩的δ34SVCDT为41.4‰~63.9‰, 平均55.7‰。同一样品中, 硫酸盐的δ34S均高于全岩的值, 但差异不大。铁丝坳组顶部含砾杂砂岩的δ13Ccarb为–11.3‰ ~ –8.3‰, 平均–9.6‰, δ13Corg为–31.7‰ ~ –30.1‰, 平均–30.9‰; 大塘坡组一段黑色页岩和锰矿石的δ13Ccarb为–12.4‰ ~ –4.6‰, 平均–8.5‰, δ13Corg为–34.3‰~ –32.6‰, 平均–33.6‰, 二者在含锰段同步下降, 有机碳含量明显升高, 说明有机质对锰矿的形成发挥了重要作用。综上提出, 大塘坡式锰矿形成于滨浅海相半封闭性的断陷盆地之中, 含锰地层中δ34S异常高的黄铁矿是在氧化还原分层明显的静水环境中, 由δ34S异常高的孔隙水硫酸盐在成岩过程中几乎全部还原形成的, 而海水硫酸盐的δ34S正异常与雪球事件、生物爆发和沉积演化等密切相关。雪球融化之后, 在断陷盆地的浅层海水中, 生物活动和光合作用强盛, 氧浓度高, 海水中Mn2+不断被氧化形成氧化锰并从海水中沉淀出来, 而深部还原缺氧富Mn2+的海水不断越过构造脊进来补充。浅层海水中微生物大量繁殖, 死亡后沉降于海底, 导致断陷盆地底部有机质大量聚集, 氧逸度急剧下降。在沉积成岩过程中氧化锰被沉积物中大量有机质全部还原为Mn2+, 有机质本身被氧化为CO2– 3, 二者结合形成菱锰矿。  相似文献   

4.
富有机质页岩中方解石脉体普遍发育,其形成过程和机制对成烃储层和成藏具有重要指示意义。本文以四川盆地南部龙马溪组为例,采用显微岩相学、阴极发光、原位微区电子探针、同位素地球化学及流体包裹体相结合的方法,分析其中的方解石脉成因,并结合地质背景探讨了成岩流体动态演化模式及其勘探意义。结果表明,研究区龙马溪组页岩发育三期方解石脉,第一期(Cal-1)近围岩或独立生长,形成于同生—准同生成岩阶段,是微生物还原作用的产物,具有富Fe、Mg、Al元素、贫Mn元素的特征,其δ~(13)C_(V-PDB)=0.06‰～4.53‰,δ~(18)O_(V-PDB)=-13.21‰～-10.79‰,n(~(87)Sr)/n(~(86)Sr)=0.719366～0.719689;第二期(Cal-2)形成于早成岩阶段,是有机质脱羧作用的产物,以相对富Fe、Mg、Mn、Al元素为特征,其δ~(13)C_(V-PDB)=-6.93‰～-0.08‰,δ~(18)O_(V-PDB)=-13.28‰～-10.05‰,n(~(87)Sr)/n(~(86)Sr)=0.719378～0.720688;第三期(Cal-3)远离围岩,形成于晚成岩阶段,是甲烷热氧化作用的产物,具有富Fe、Mg、Mn元素,不含Al元素的特征,其δ~(13)C_(V-PDB)=-19.00‰～-12.64‰,δ~(18)O_(V-PDB)=-9.08‰～-6.65‰,n(~(87)Sr)/n(~(86)Sr)=0.719855～0.721342。通过对方解石脉成因及流体来源刻画,结合龙马溪组页岩热演化史,三期方解石脉的成岩演化对页岩的储集空间具有改善作用,有利于页岩气的勘探开发。  相似文献   

5.
羌塘北缘开心岭—乌丽冻土区沿隐伏断层发育多处冷泉含水溶解烷烃,采用水溶烃组分和甲烷的稳定碳、氢同位素特征对其成因开展了分析研究。结果表明,开心岭—乌丽冻土区水溶烃组分中甲烷含量比例高达99.83%~99.96%,同时伴随有少量乙烷、丙烷,另含微量的乙烯和丙烯。开心岭一带水溶烃甲烷δ13CPDB值介于-46.5‰~-55.1‰,δDVSMOW值为-281.0‰~-342.0‰;乌丽一带水溶烃甲烷δ13CPDB值介于-47.8‰~-58.9‰,δDVSMOW值为-339.0‰~-346.0‰,指示水溶烃甲烷为有机成因,但气源较复杂,利用δ13CCH4-δDCH4、δ13C1-C1/(C2+C3)等成因图解判别,得出甲烷主要属微生物气,次之为热解成因气,混有少量原油伴生气。推断甲烷主要为有机质在微生物作用下分解的烃类气体或次生生物气,与晚二叠世那益雄组含煤烃源岩有关,气源条件暗示该地区冻土带200~500 m深度内有利于微生物成因气为主的甲烷天然气水合物形成。  相似文献   

6.
肖术安 《地质与勘探》2016,52(2):228-238
易门铜厂矿床是滇中易门铜矿带中的Cu品位较低的大型矿床,是矿带中的一种代表性矿床。矿区发育沉积-成岩型铜矿(铜厂式)和热液脉状铜矿(大尖山式)两种矿(化)体,成矿地质作用较特殊。本文系统分析两类矿体和赋矿碳酸盐地层的C、O同位素组成。结果表明,铜厂式矿石中白云石的δ~(13)C_(PDB)=-3.7‰~1.4‰,平均值-0.1‰,δ~(18)O_(SMOW)=19.7‰~21.7‰,平均值20.8‰,与赋矿碳酸盐地层(落雪组)中的白云石C、O同位素组成一致,均在正常海相沉积碳酸盐岩的范围,且受成岩期后作用的影响小,具有典型的沉积-成岩成因标志。尖山式矿体的脉石矿物方解石的δ~(13)C_(PDB)=-3.7‰~0.1‰(均值为-1.5‰),δ~(18)O_(SMOW)=11.9‰~17.0‰(均值为14.1‰),与沉积-成岩型矿体和赋矿碳酸盐地层的C、O同位素组成明显不同,在δ~(13)C_(PDB)-δ~(18)O_(SMOW)图上集中于岩浆碳酸岩与海相碳酸盐岩之间的狭小范围内,指示其成矿流体与幔源或深部岩浆活动有关,为壳-幔混合流体。其中壳源组分可能主要由矿区碳酸盐地层提供,而幔源组分则可能与晋宁-澄江期基性岩浆活动过程中的去气作用有关。C、O同位素组成证据说明,铜厂矿区层状铜矿和脉状铜矿的成矿作用类型不同,成矿流体也不具同源性,是典型的沉积-成岩型+热液叠加型矿床。  相似文献   

7.
通过对西太平洋34件海水样品的稀土元素（REY:REE+Y）测试及其与研究区富钴结壳稀土耦合特征分析,揭示了海水稀土特征及其成因.海水的稀土含量随水深呈现逐渐增加的趋势,∑ REY范围为14.0×10-12~65.5×10-12,平均值为31.9×10-12,其中Y的绝对值（均值为6.0×10-12~24.1×10-12）和相对值（（Y/Ho）N均值为1.98）均较高,La含量次之（均值为1.8×10-12~11.6×10-12）,Ce含量相对较低（均值为2.4×10-12~8.8×10-12）,δCe范围为0.33~1.03（均值为0.66）,（La/Yb）N平均值为0.71.海水稀土元素北美页岩标准化后显示左倾模式,具有显著的Ce负异常、Y正异常和无明显的Eu异常特征.研究区普遍发育水成成因的富钴结壳,即其稀土元素和其他组分均源自海水.富钴结壳的稀土含量相对海水富集6~7个数量级,其Ce正异常和Y负异常的稀土模式与海水构成良好的耦合关系,指示富钴结壳类组分对海水稀土清扫具有选择性,是造成海水稀土模式的重要因素.海山上发育的磷块岩以及周围盆地深海泥中的磷酸盐组分,它们具有较高的稀土含量和类似于海水的稀土模式,指示海洋磷酸盐消耗稀土时并未分馏而是继承海水模式.海水独特的稀土模式特征是补给与消耗平衡作用的结果,铁锰氧化物和海洋磷酸盐是两种典型的海洋自生组分,它们对海水稀土特征的形成至关重要.   相似文献   

8.
《地学前缘》2017,(4):66-77
对珠江口盆地东部陆坡GMGS 08C孔的3层自生碳酸盐岩(结核状)和有孔虫(底栖和浮游)开展高分辨率氧碳同位素分析和AMS~(14) C测年,第1层自生碳酸盐岩δ~(13) C为-38.85‰,第2、3层的δ~(13) C介于-41.36‰~-56.74‰,平均值-51.64‰,均低于-40‰。δ~(18) O值介于2.94‰~4.18‰,平均值3.68‰,明显偏重。这表明其为天然气水合物分解的产物,形成于微生物对甲烷的缺氧氧化作用,甲烷主要源自生物成因;自生碳酸盐岩层位的底栖有孔虫Uvigerina peregrina和浮游有孔虫Globigerinoides ruber的δ~(13) C值几乎同时出现极负偏,最低值分别达到-12.17‰和-9.06‰,有孔虫δ~(18) O总体上正偏,最大正偏幅度达1.50‰,说明其负偏与后期源于甲烷厌氧氧化作用(Anaerobic Oxidation of Methane,简称AOM)的成岩作用有关。自生碳酸盐岩及其与有孔虫异常碳(偏负)氧(偏正)、粥状沉积是GMGS 08C孔水合物分解甲烷渗漏的重要指标,据此推断该孔在末次冰期(MIS2—MIS3)发生过至少2次天然气水合物分解释放-冷泉甲烷渗漏活动,分别距今36ka和31~26ka,主要发生在低海平面期,说明冷泉活动明显受海平面变化影响。  相似文献   

9.
塔里木陆块西北缘萨热克砂岩型铜矿床构造演化、流体演化与成矿之间具有密切关系,处于一个统一系统中。矿床成岩期方解石中包裹体水的δD值为-65.3‰~-99.2‰,改造成矿期石英包裹体水的δD值为-77.7‰~-96.3‰,成岩成矿期成矿流体δ~(18)OH_2O变化范围为-3.22‰~1.84‰,改造成矿期成矿流体δ~(18)OH_2O变化范围为-4.26‰~5.14‰,指示萨热克铜矿成岩期、改造期成矿流体主要为中生代大气降水及其经水岩作用而成的盆地卤水。矿石中辉铜矿δ~(34)S值为-24.7‰~-15.4‰,指示硫主要源自硫酸盐细菌与有机质还原,部分源于有机硫。构造与成矿流体演化对砂岩铜矿成矿起关键制约作用。盆地发展早期强烈的抬升运动使盆地周缘基底与古生界剥蚀,为富铜矿源层的形成提供了丰富物源,至晚侏罗世盆地发展晚期,长期演化积聚的巨量含矿流体在库孜贡苏组砾岩胶结物及裂隙中富集,在萨热克巴依盆地内形成具有经济意义的砂岩型铜矿床。  相似文献   

10.
碳酸盐胶结物是古流体活动的产物,蕴含着成岩环境、成岩流体演化等方面的有益地质信息。综合运用岩石学、矿物学和地球化学方法,对柴北缘西段鄂博梁构造带侏罗系、古近系、新近系储层中普遍存在的碳酸盐胶结物的成因机制进行了研究。结果表明,研究区碳酸盐胶结物以方解石和含铁方解石为主。鄂博梁I号构造主要见方解石,其碳、氧同位素分布范围较大:-13.47‰ <δ13CPDB <2.54‰,-15.93‰ <δ18OPDB <-4.74‰,成因多种多样,与有机质脱羧、同生-准同生、甲烷生成等作用有关;鄂博梁III号-鸭湖构造则主要见含铁方解石,其碳、氧同位素分布集中:-4.24‰ <δ13CPDB <-1.99‰,-11.17‰ <δ18OPDB <-9.41‰,为沉积压实水沉淀而成。碳酸盐胶结物的成因揭示了鄂博梁构造带无机-有机流体的活动信息,从而为该地区油气成藏研究提供了重要依据。  相似文献   

11.
Sedimentological, mineralogical, stable carbon and oxygen isotope determinations and biomarker analyses were performed on siderite concretions occurring in terrestrial silts to understand their formation and to characterize the sedimentary and diagenetic conditions favouring their growth. High δ13C values (6·4‰ on average) indicate that siderite precipitated in an anoxic environment where bacterial methanogenesis operated. The development of anoxic conditions during shallow burial was induced by a change in sedimentary environment from flood plain to swamp, related to a rise of the ground‐water table. Large amounts of decaying plant debris led to efficient oxygen consumption within the pore‐water in the peat. Oxygen depletion, in combination with a decrease in sedimentation rate, promoted anoxic diagenetic conditions under the swamp and favoured abundant siderite precipitation. This shows how a change in sedimentary conditions can have a profound impact on the early‐diagenetic environment and carbonate authigenesis. The concretions contain numerous rhizoliths; they are cemented with calcium‐rhodochrosite, a feature which has not been reported before. The rhodochrosite cement has negative δ13C values (?16·5‰ on average) and precipitated in suboxic conditions due to microbial degradation of roots coupled to manganese reduction. The exceptional preservation of the epidermis/exodermis and xylem vessels of former root tissues indicates that the rhodochrosite formed shortly after the death of a root in water‐logged sediments. Rhodochrosite precipitated during the initial stages of concretionary growth in suboxic microenvironments within roots, while siderite cementation occurred simultaneously around them in anoxic conditions. These suboxic microenvironments developed because oxygen was transported from the overlying oxygenated soil into sediments saturated with anoxic water via roots acting as permeable conduits. This model explains how separate generations of carbonate cements having different mineralogy and isotopic compositions, which would conventionally be regarded as cements precipitated sequentially in different diagenetic zones during gradual burial, can form simultaneously in shallow burial settings where strong redox gradients exist around vertically oriented permeable root structures.  相似文献   

12.

Sideritic ironstones in Tertiary lacustrine oil shale from the Lowmead and Duaringa Basins in Queensland, contain two distinctive types of siderite in the ironstone bands: sphaerosiderite in the mudstone and coal, and finely crystalline siderite in the lamosite. The petrological evidence indicates that the siderite in the ironstone bands formed eogenetically by growing displacively within the soft sediment. Chemically the siderite is very pure though the sphaerosiderite sometimes shows compositional zoning. Stable oxygen and carbon isotope analyses of the siderite show a wide range of values from ‐12.8‰ to ‐2.4 %0 δ18O (PDB) and ‐5.5‰ to +12.9‰ δ13C (PDB) for the Lowmead Basin; and ‐9.6‰ to ‐1.2‰ δ18O (PDB) and ‐18.6‰ to +16.4‰ δ13C (PDB) for the Duaringa Basin. The oxygen isotope data indicate that the siderite formed in freshwater environments but not in isotopic equilibrium with the formation waters. Kinetic factors offer the most plausible explanation for the anomalously light δ18O values of many of the siderites. The carbon isotope data show that the carbonate for the formation of the siderite originated predominantly from methanogenic fermentation processes but there was also the varying influence of bacterial oxidation processes. The different petrological and isotopic characteristics of the ironstones broadly reflect variations in their depositional environments and the variable eogenetic conditions in which the siderite formed. There is no suitable single model to explain the genesis of all the different types of ironstones other than that a synsedimentary iron‐enrichment process is involved.  相似文献   

13.
The Lower Permian Aldebaran Sandstone is the principal hydrocarbon reservoir in the Denison Trough (Bowen Basin), east-central Queensland, Australia. It accumulated in a wide range of fluvio-deltaic and nearshore marine environments. Detailed petrological study of the unit by thin section, X-ray diffraction, scanning electron microscopy, electron microprobe and isotopic analysis reveals a complex diagenetic history which can be directly related to depositional environment, initial composition and burial-temperature history. Early diagenetic effects included the precipitation of pyrite, siderite and illite-smectite rims (δ18O (SMOW) =+8.9 to + 11.3‰). Deep burial effects included physico-chemical compaction and the formation of quartz overgrowths, siderite (δ13C(PDB) =?34.0 to + 11.5‰, δ18O =?0.7 to +22.7‰), illite/illite-smectite and ankerite (δ13C=?9.3 to ?4.9‰) δ18O=+ 7.6 to + 14.4‰). Involved fluids were in part ‘connate meteoric’ water derived from compaction of the underlying freshwater Reids Dome beds. Important post-maximum burial effects, controlled by deep meteoric influx from the surface, were ankerite and labile grain dissolution and formation of kaolinite (δ18O=+7.8 to +8.9‰, δD=?115 to ?99‰), calcite (δ13C=?9.5 to +0.9‰, δ18O=+9.0 to +20.0‰) and dawsonite (δ13C=?4.0 to +2.3‰, δ18O=+9.8 to +19.8‰), the formation of dawsonite reflecting eventual stagnation of the aquifer. Entrapment of contained hydrocarbons was a relatively recent event which may be continuing today. Reservoir quality varies from marginal to good in the west to poor in the east, with predictable trends being directly linked to depositional environment and diagenesis.  相似文献   

14.
Siderite (FeCO3) is a widespread minor diagenetic mineral in clastic sedimentary basins. Although eodiagenetic authigenesis of siderite is well-known, siderite formed during burial diagenesis shows habits and chemical compositions that are poorly understood. This study tests the hypothesis that diagenetic siderite cements in sandstones in the Scotian Basin, offshore eastern Canada, show systematic variability in chemistry and habit that is a response to recrystallization and changing composition of basinal fluids. Mineral textures were determined from backscattered electron images, and chemistry mostly from electron microprobe analyses. Five chemical types of siderite are identified using k-means cluster analysis, based on the amount of substitution of Ca, Mg and Mn for Fe. Eodiagenetic microcrystalline coated grains, concretions and intraclasts in sandstones are principally Fe-rich siderite and locally have recrystallised to blocky equant crystals. Mesodiagenetic Mg-rich siderite partly replaced these equant crystals and also framework mica and K-feldspar grains, showing textural evidence for coupled dissolution–reprecipitation. Slender Mg-rich siderite rhombs (lozenges, bladed or wheat-seed siderite) have precipitated before and after the formation of quartz overgrowths in geochemical microenvironments. Magnesium substitution reflects Mg-rich formation waters resulting from smectite to illite conversion. Equivalent Ca-rich siderite occurs where sandstones overlie a Jurassic carbonate bank. Late Mn-rich siderite has complex textures resembling those of Mississippi-Valley type ores, with spheroidal rims, a honeycomb-like mesh and concentric infill around secondary pores. It also occurs in veins or replacing intraclasts, post-dating late ferroan-calcite cements in sandstones that show strong dissolution by hot basinal brines. The Ca, Mg and Mn content of diagenetic siderite, coupled with textural evidence for recrystallization, can thus be used to track changes in ambient formation fluids. Siderite habits and chemistry described from the Scotian Basin are found in many clastic basins, suggesting that the observed recrystallization textures and variation in chemical type are of broad application.  相似文献   

15.
The occurrence of early diagenetic Ca‐rhodochrosite [(Mn,Ca)CO3] is reported in association with ‘griotte’‐type nodular limestones from basinal settings in the geological record; however, without the comparison of analogous modern examples, the controls on precipitation remain speculative. Here the findings of four layers of primary Ca‐rich rhodochrosite recovered from a modern deep‐sea setting in the Eastern Equatorial Pacific, from bioturbated sediments 300 m below sea floor, are reported (Ocean Drilling Program, Leg 201, Site 1226). The mineralogy is similar to cements in burrows recovered during Deep Sea Drilling Project Leg 68 at Eastern Equatorial Pacific Site 503 and from Ca‐rhodochrosite laminae in sediments of the central Baltic Sea. Petrographic relationships and constant oxygen isotopic compositions in the Ca‐rhodochrosite around 5‰ at all depths indicate a shallow burial depth of formation. The onset of 1‰ heavier oxygen isotope composition of Ca‐rhodochrosite at Site 503, about 30 m below the Pliocene/Pleistocene boundary, further suggests that precipitation occurs in the range of 30 m below sea floor. The approximate depth of formation allowed an approximate empirical fractionation factor for marine Ca‐rhodochrosite to be constrained that strongly differs from previously published theoretical values. Based on the approximate precipitation depth, authigenic Ca‐rhodochrosite forms within the SO42?‐reduction zone. Moderately negative δ13C values (around ?3‰) and total organic carbon lower than 2 wt% indicate a relatively low contribution of CO32? from organic C mineralization within the expanded redox zonation in the Eastern Equatorial Pacific. It is suggested that the alkalinity is increased by a rise in pH at focused sites of Mn‐reduction coupled with S2? oxidation. High concentrations of Mn‐oxide can accumulate in layers or burrows because of Mn‐cycling in suboxic sediments as suggested for the Baltic Sea Ca‐rhodochrosites. This study demonstrates how early diagenetic precipitates document biogeochemical processes from past diagenetic systems.  相似文献   

16.
The oxygen isotope compositions of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel, have been used to identify porewater types during diagenesis. Changes in porewater composition can be related to major geological events within southern Israel. In particular, saline brines played an important role in late (Pliocene-Pleistocene) dolomitization of these rocks. Diagenetic carbonates included early siderite (δ18OSMOW=+24.4 to +26.5‰δ13CPDB=?1.1 to +0.8‰), late dolomite, ferroan dolomite and ankerite (δ18OSMOW=+18.4 to +25.8‰; δ13CPDB=?2.1 to +0.2‰), and calcite (δ18OSMOW=+21.3 to +32.6‰; δ13CPDB=?4.2 to + 3.2‰). The petrographic and isotopic results suggest that siderite formed early in the diagenetic history at shallow depths. The dolomitic phases formed at greater depths late in diagenesis. Crystallization of secondary calcite spans early to late diagenesis, consistent with its large range in isotopic values. A strong negative correlation exists between burial depth (temperature) and the oxygen isotopic compositions of the dolomitic cements. In addition, the δ18O values of the dolomitic phases in the northern Negev and Judea Mountains are in isotopic equilibrium with present formation waters. This behaviour suggests that formation of secondary dolomite post-dates the tectonic activity responsible for the present relief of southern Israel (Upper Miocene to Pliocene) and that the dolomite crystallized from present formation waters. Such is not the case in the Central Negev. In that locality, present formation waters have much lower salinities and δ18O values, indicating invasion of freshwater, and are out of isotopic equilibrium with secondary dolomite. Recharge of the Inmar Formation by meteoric water in the Central Negev occurred in the Pleistocene, and halted formation of dolomite.  相似文献   

17.
萨瓦亚尔顿金矿床成矿地质特征及同位素组成   总被引：6，自引：1，他引：5  
西南天山的萨瓦亚尔顿金矿床,赋存于中-上石炭统浊积岩系中.矿化受构造破碎带控制,以含矿的石英细（网）脉和含矿的石英-碳酸盐细（网）脉形式产出.矿体呈似层状和透镜状,矿石的矿物组成和矿石类型复杂,矿石中金与黄铁矿、毒砂、黄铜矿等硫化物密切共生,金矿物以银金矿为主.铅、硅、硫同位素组成表明,成矿物质主要来自深部较老的地层和岩石.氢、氧、碳同位素特征显示,成矿作用乃通过大气降水补给的地下水渗入深部,经加热循环并溶滤围岩中的矿质,迁移到减压空间和有利岩性层中而成矿.成矿时代属燕山中-晚期.  相似文献   

18.
菱铁矿是前寒武纪条带状铁建造(BIF)中重要的矿物组分和古海洋信息载体,但它可能具有原生、早期成岩和晚期成岩多种成因,这在一定程度上限制了其在古海洋条件分析中的应用。虽然前人对菱铁矿开展了广泛的地球化学分析,但在岩相学研究方面相对薄弱。为进一步揭示BIF中菱铁矿的成因机制,以山西代县羊角沟矿区新太古界柏芝岩组的BIF为研究对象,开展了系统的岩相学工作。研究表明,该BIF主要由厘米级交互的富铁与富硅条带构成,其中普遍缺少水体扰动沉积构造,偶见交错层理和风暴碎屑,表明主要沉积于风暴浪基面之下。菱铁矿的主要产出形式有3种:(1)亚毫米级条带,其内"悬浮"有风暴成因碎屑颗粒,具有水柱或沉积物/水界面的原生成因特征;(2)在富铁条带中的晶体间隙充填,可能为早期成岩成因;(3)富硅条带中存在绿泥石层间脉状充填或截切石英和铁白云石的脉体,具有晚期成岩成因。原生菱铁矿的产出,表明新太古代在风暴浪基面之下的海水强烈缺氧、富铁并具有低硫酸盐浓度的特征。尽管原生菱铁矿条带的产出表明菱铁矿具有反映海洋化学条件的潜力,但多种成因菱铁矿的同时产出,也要求在应用菱铁矿分析古海洋条件时应当分组构进行。  相似文献   

19.
黔西织金矿区乐平世煤系中的菱铁矿以多种微观形态产出,基于镜下薄片观测、泥岩微量元素分析,探讨了菱铁矿 成因及演化。研究表明菱铁矿可划分为第一世代的胶状集合体、第二世代圈层结构发育不良的球粒及第三世代圈层结构发 育完好的鲕粒与菱面体三个成岩世代产物。菱铁矿胶状集合体是在成矿组分（Fe2+ 与CO32-） 浓度达到超饱和状态时快速结 晶形成的;圈层结构发育不良的菱铁矿球粒是成矿物质围绕第一世代形成的菱铁矿胶粒聚集而成;圈层结构发育完好的菱 铁矿鲕粒是大量放射状菱铁矿线晶以第二世代的球粒为核心连续共轴生长而成,晚二叠世脉动式的海侵可能是菱铁矿在结 晶非平衡态与平衡态与之间往复循环驱动因素,最终形成了同心圈层结构,而同心圈层发育完好的菱面体状菱铁矿可能是 成矿条件的变化促使鲕粒从放射状生长向自形菱面体生长而成。  相似文献   

20.
菱铁矿是前寒武纪条带状铁建造(BIF)中重要的矿物组分和古海洋信息载体,但它可能具有原生、早期成岩和晚期成岩多种成因,这在一定程度上限制了其在古海洋条件分析中的应用。虽然前人对菱铁矿开展了广泛的地球化学分析,但在岩相学研究方面相对薄弱。为进一步揭示BIF中菱铁矿的成因机制,以山西代县羊角沟矿区新太古界柏芝岩组的BIF为研究对象,开展了系统的岩相学工作。研究表明,该BIF主要由厘米级交互的富铁与富硅条带构成,其中普遍缺少水体扰动沉积构造,偶见交错层理和风暴碎屑,表明主要沉积于风暴浪基面之下。菱铁矿的主要产出形式有3种: (1)亚毫米级条带,其内“悬浮”有风暴成因碎屑颗粒,具有水柱或沉积物/水界面的原生成因特征;(2)在富铁条带中的晶体间隙充填,可能为早期成岩成因;(3)富硅条带中存在绿泥石层间脉状充填或截切石英和铁白云石的脉体,具有晚期成岩成因。原生菱铁矿的产出,表明新太古代在风暴浪基面之下的海水强烈缺氧、富铁并具有低硫酸盐浓度的特征。尽管原生菱铁矿条带的产出表明菱铁矿具有反映海洋化学条件的潜力,但多种成因菱铁矿的同时产出,也要求在应用菱铁矿分析古海洋条件时应当分组构进行。  相似文献   

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