Were kinetics of Archean calcium carbonate precipitation related to oxygen concentration?

Archean carbonates commonly contain decimetre- to metre-thick beds consisting entirely of fibrous calcite and neomorphosed fibrous aragonite that precipitated in situ on the sea floor. The fact that such thick accumulations of precipitated carbonate are rare in younger marine carbonates suggests an important change in the modes of calcium carbonate precipitation through time. Kinetics of carbonate precipitation depend on the concentration of inhibitors to precipitation that reduce crystallization rates and crystal nuclei formation, leading to kinetic maintenance of supersaturated solutions. Inhibitors also affect carbonate textures by limiting micrite precipitation and promoting growth of older carbonate crystals on the sea floor. Fe2+, a strong calcite-precipitation inhibitor, is thought to have been present at relatively high concentrations in Archean seawater because oxygen concentrations were low. The rise in oxygen concentration at 2.2-1.9 Ga led to the removal of Fe2+ from seawater and resulted in a shift from Archean facies, which commonly include precipitated beds, to Proterozoic facies, which contain more micritic sediment and only rare precipitated beds.     

The role of fluids in the formation and subsequent development of early continental crust

A petrogenetic model is developed to explain the evolution and geochemical character of granitic rocks in early Archean (pre 3.6 Gyr) continental crust taking into account the following important geological constraints, viz.:

1. High geothermal gradients (probably in excess of 90 ° C/km) and resulting widespread granulite facies metamorphism even at relatively shallow depths
2. The fractionation of certain major and trace elements under granulite facies conditions
3. The composition and geochemical behaviour of fluids which emanate from or pass through terrains undergoing granulite facies metamorphism viz. carbonic fluids containing significant amounts of SO₂ and halogens.

In this model tonalitic and trondhjemitic intrusives are regarded as being derived dominantly by partial melting of mafic granulite. The ubiquitous potassic granites, which typical post-date sodic plutonic activity are interpreted to be anatectic melts generated under granulite or amphibolite facies conditions from the previously formed ‘plagiogranites’. The presence of a postulated granulite facies source area for Archean tonalitic rocks, and the geochemical character of fluids which accompany metamorphism under such conditions explains the HREE geochemistry of these suites and casts doubt on the validity of applying currently used trace element fractional melting or crystallization models to these terrains. Similarly it suggests that petrogenetic interpretations based on Sr and Pb isotopic systems must be reevaluated because of the extreme mobility of both parent and daughter elements under granulite facies conditions.     

Exsolution of dolomite and application of calcite–dolomite solvus geothermometry in high‐grade marbles: an example from Skallevikshalsen,East Antarctica

Calcite–dolomite solvus geothermometry is a versatile method for the estimation of metamorphic temperature because of its simplicity. However, in medium‐ to high‐grade metamorphic rocks the accuracy of estimating temperature by the integration of unmixed dolomite and calcite is hampered by the heterogeneous distribution of unmixed dolomite, difficulties in distinguishing between preexisting and exsolved dolomite and demarcating grain boundaries. In this study, it is shown that calcite–dolomite solvus thermometry can be applied to calcite inclusions in forsterite and spinel for the estimation of peak metamorphic temperature in granulite facies marbles from Skallevikshalsen, East Antarctica. The marbles are comprised of a granoblastic mineral assemblage of calcite + dolomite + forsterite + diopside + spinel + phlogopite ± apatite, characteristic of granulite facies metamorphic conditions. Forsterite, spinel and apatite frequently contain ‘negative crystal’ inclusions of carbonates that display homogeneously distributed dolomite lamellae. On the basis of narrow ranges of temperature (850–870 °C) recorded from carbonate inclusions compared with the range from matrix carbonate it is regarded that the inclusion carbonates represent a closed system. Furthermore, this estimate is consistent with dolomite–graphite carbon isotope geothermometry, and is considered to be the best estimate of peak metamorphic temperature for this region. Matrix calcite records different stages of retrograde metamorphism and re‐equilibration of calcite that continued until Mg diffusion ceased at ～460 °C. Electron backscattered diffraction (EBSD) results together with morphological features of unmixed coarse tabular dolomite suggest anisotropic diffusion and mineral growth are influenced by crystallographic orientation. Identification of sub‐grain boundaries and formation of fine‐grained unmixing in calcite rims suggest the presence of grain boundary fluids in the late retrograde stages of metamorphic evolution. These results, thus, demonstrate the usefulness of carbonate inclusion geothermometry in estimating the peak metamorphic temperatures of high‐grade terranes and the application of EBSD in understanding the unmixing behaviour of minerals with solid solutions.     

贺兰山——阿拉善地区下、中前寒武系的划分对比及其变质、成矿作用特征

据近期成果,贺兰山—阿拉善地区出露的巨厚变质杂岩可划分为中太古界贺兰山群和叠布斯格群(其全岩Rb—Sr等时年龄为3108.3和3218.8Ma),上太古界阿拉善群和下元古界的赵池沟群、阿拉坦敖包群;它们具不同的变质矿物共生组合,太古界变质岩属低压高温变质的麻粒岩相;下元古界为低—低中压区域动力(热流)变质的绿片岩相岩石。太古界有较强的混合岩化、花岗岩化作用,并蕴藏有铁、石墨、矽线石、刚玉等多种矿产。     

Variations in Neoarchean microbialite morphologies: clues to controls on microbialite morphologies through time

The Neoarchean Carawine Formation, Hamersley Group, Western Australia is a carbonate ramp that preserves diverse microbial structures which are characteristic of specific depositional environments. These distinctive structures are distributed in five shallow subtidal and two deeper‐water facies in the Oakover area of the Carawine Formation. The shallow subtidal facies are composed of biohermal and bedded stromatolites, centimetre‐scale ridge‐shaped microbialites and wavy‐laminated microbialites. The deeper‐water facies are composed of fenestrate microbialites, planar laminated dolostone and dolostone with rolled‐up microbial laminae. Microbialites in the Carawine Formation lie within a continuum of Archean to Proterozoic microbial facies. Some shallow‐water microbial facies in the Carawine Formation are similar to Proterozoic facies, such as large bioherms internally composed of a variety of stromatolite morphologies. In contrast, fenestrate microbialites grew in quiet subtidal environments and are common in Archean rocks but have not been documented in similar Proterozoic environments. The similarity of shallow‐water facies across the Archean–Proterozoic transition, before and after the oxidation of the atmosphere and surface oceans, indicates that stromatolite growth in shallow subtidal environments was not strongly affected by the chemical changes associated with oxidation of the oceans or by biological responses to those chemical changes. Rather, stromatolite morphology was controlled mostly by the physical environment and the corresponding biological responses to that environment. In contrast, the absence of fenestrate microbialites from Proterozoic deep subtidal environments suggests that the morphology of deep subtidal microbial structures was influenced by chemical or biological changes that occurred in association with oxidation of the surface oceans.     

中国东部大陆尺度地球化学走廊带碳酸盐岩稀土元素分布特征与影响因素

碳酸盐岩是地球表层岩石圈的重要组成部分,其化学组成可提供沉积环境与海洋水体演化等信息,然而,前人对碳酸盐岩中稀土等元素的分布与变化特征关注不足。本文选择穿越中国东部6个一级大地构造单元的3条地球化学走廊带,系统采集了582件碳酸盐岩地层样品,并准确分析了包括稀土元素(REE)在内的81项指标的含量。结果表明,中国东部地球化学走廊带碳酸盐岩稀土元素(REE＋Y)总量为(0.59～183)×10-6,均值为24.0×10-6,纯净碳酸盐岩(CMC含量≥99％)均值为4.80×10-6。PAAS标准化后其显示具有轻稀土相对于中稀土和重稀土略亏损、δEu轻微正异常、δCe中度负异常等特征。白云岩中稀土含量、LREE/HREE值一般低于石灰岩;砂泥质含量相近时,前中生代各时代碳酸盐岩稀土分布模式相差不大,各构造单元稀土分布特征基本相似;与其他时代相比,中生代及中新元古代碳酸盐岩具有相对较平坦的稀土分布模式。研究表明,碳酸盐岩中稀土分布受碎屑物质影响明显,表现为稀土元素含量与碳酸根负相关,与碎屑物质相关元素(Si、Ti、Rb、Cs、Th、Zr等)、黏土相关元素(Al、Fe、K等)等正相关。成岩过程及白云化过程对较纯净碳酸盐岩中稀土分布特征影响不明显。我国古生代纯净碳酸盐岩分布模式受控于海相环境,其分布模式与现今海水相近;中生代纯净石灰岩受到陆相或海陆交互相的影响,具有较平坦的稀土分布模式。氧化还原条件对δCe的影响较δEu更为明显,δCe值受海相环境控制,极端正异常值(δCe＞1.3)受到还原环境或/和热液影响。若假定海水中REE自中元古代至今无太大变化,各时代稀土元素分配系数均值介于103.55～102.39,分配系数差异是造成碳酸盐岩中轻稀土亏损、Ce负异常及Y正异常的主要原因。微生物(席)可富集稀土等金属元素并改变沉积环境,这可能是造成中新元古界碳酸盐岩较平坦的稀土分布模式的主要原因。     

鲁山太华群麻粒岩相岩石形成的地球化学限制

鲁山太华群麻粒岩相岩石形成的地球化学限制徐启东，高山，刘庆生（中国地质大学，武汉４３００７４）主题词麻粒岩相岩石，ＬＩＬ元素亏损，下地壳太华群提要河南鲁山太古宙高级区表壳岩中的麻粒岩相岩石及相关的角闪岩相岩石与世界其它地区麻粒岩相岩石相比并没有明显的...     

热带地区碳酸盐岩上覆红色风化壳的成因机理及元素演化

开展热带岩溶地区红色风化壳元素地球化学演化规律研究,有助于丰富碳酸盐岩风化成土理论的认识。在越南北部选取典型的碳酸盐岩风化剖面,分析热带气候条件下碳酸盐岩上覆红色风化壳中主量元素的物质来源和演化特征。结果表明:无论Ti/Zr的元素比值分析,Hf-Zr、Nb-Ta及Sm-Nd的元素对协变分析,还是上地壳元素平均值(UCC)标准化分析,两个剖面的上覆风化壳均显示原地残积的特征,即两个剖面是碳酸盐岩的原位风化产物。碳酸盐岩风化成土过程中,CaO、MgO淋失明显,Al_2O_3和Fe_2O_3发生富集,显示两个剖面均经历较强的风化过程,但是白云岩和灰岩剖面有一定的分异特征。越南北部白云岩风化剖面从基岩到上部土层显示出稳定的Ti-Fe元素共富集特征,而灰岩剖面中Fe的增长速率明显超过Ti。白云岩上覆风化壳经历了强烈的风化作用,其脱硅作用弱于灰岩风化剖面,而富集铝的作用强于灰岩。迁移系数的演化规律说明两个剖面中长石成分(钾长石、钠长石等)或次生矿物(伊利石等)在风化成土过程中逐渐分解,同时Al、Fe、Si等稳定元素的在风化剖面中不断富集。     

天津蓟县中元古界雾迷山组微指状叠层石及其对1250 Ma±叠层石衰减事件的响应

天津蓟县中元古界雾迷山组是一套厚度超过3000,m的叠层石碳酸盐岩沉积序列,在该序列中潮下相叠层石生物层、凝块石生物丘与潮坪相泥晶白云岩、潟湖相白云质泥页岩一起构成若干个环潮坪型米级旋回——"雾迷山旋回层"。在雾迷山组下部发育微指状叠层石,并被古生物学家定义为"Pseudogymnosolen mo-panyuensis-Scuphus-Yangzhuang columnaris"组合,即假裸枝叠层石科叠层石,沉积学家将其解释为元古代文石(灰华)海底沉淀物所构成的叠层石,代表从太古代海底结壳状文石沉淀物组成的叠层石到新元古代碎屑结构相的泥晶碳酸盐岩叠层石过渡时期的特殊产物。因此,雾迷山组巨厚的叠层石碳酸盐岩沉积序列,记录了元古代文石(灰华)海底沉淀物所构成的特殊的叠层石大规模消亡的层位,为研究前寒武纪以叠层石为代表的微生物碳酸盐岩所经历的漫长而复杂的地质历史演变提供了宝贵的材料。     

Petrological significance of manganese carbonate inclusions in spessartine garnet and relation to the stability of spessartine in metamorphosed manganese-rich rocks

Idioblastic spessartine garnet pervasively developed in Mn-rich rocks and impure manganese carbonate ore at the Lower Proterozoic Nsuta manganese deposit, Western Ghana, contains abundant inclusions of micritic and microconcretionary carbonates and, to a lesser extent, quartz. Detailed mineralogical and microprobe studies indicate all the carbonate phases (i.e. carbonate inclusions in garnet, carbonates coexisting with garnet and carbonates not directly in contact with garnet, the latter hereafter referred to as matrix carbonates) lie within the rhodochrosite-kutnahorite solid solution series, i.e. ~Mn_55-80(Ca + Mg)_20-45CO₃ to Ca₄₂(Mn + Mg)₅₈(CO₃)₂. Minor compositional differences occur in the various carbonate phases, but partition of major elements among coexisting phases indicate most carbonate minerals strongly fractionate Ca and Mg over coexisting spessartine. The nature, composition and textural relationship of coexisting minerals and inclusions in porphyroblastic spessartine indicate that the latter formed from metamorphic reactions in which rhodochrosite and/or kutnahorite and quartz were consumed, in part corroborating earlier observations on a rhodochrosite precursor for spessartine. Spessartine formation is thus envisaged to have taken place when the predominantly Mn carbonate-quartz assemblage became unstable in the presence of minor amounts of an unknown aluminous phase. Because all the carbonates appear to be low-temperature phases with no indications of significant recrystallisation or homogenisation, it could be argued that the spessartine + rhodochrosite - kutnahorite - quartz - pyrite assemblage stabilised during very low-grade greenschist facies metamorphism under relatively low but uniform f_O2 conditions. These observations also suggest the stability field of spessartine could extend to relatively lower temperatures than currently envisaged.     

Do Archean chemical sediments record ancient seawater rare earth element patterns?

Rare earth elements (REE) concentrations of Archean and Proterozoic chemical sediments are commonly used as proxies to study secular trends in the geochemistry of Precambrian seawater. In addition, similarities in the REE signatures of Archean chemical sediments and modern seawater have led researchers to argue that some Archean rocks originated as biochemical precipitates (i.e., microbial carbonates) in shallow marine (e.g., peritidal) environments. However, terrestrial waters, including river water and groundwater, also commonly exhibit REE fractionation patterns that resemble modern seawater. Here, we present the seawater-like REE data for groundwaters from central México as additional evidence that these patterns are not unique to the marine environment. The shale-normalized REE patterns of the groundwaters are compared to those of modern seawater (open ocean and nearshore), Holocene reefal microbial carbonates and corals, and Archean chemical sediments using statistical means (i.e., ANOVA and Wilcoxon analyses) in order to quantify the similarities and/or differences in the REE patterns. Shale-normalized (SN) Ce anomalies and measures of REE fractionation [i.e., (La/Yb)_SN, (Pr/Yb)_SN, (Nd/Yb)_SN, and (Gd/Yb)_SN] of the central México groundwater samples are statistically indistinguishable from those of modern seawater. Moreover, except for differences in the Ce anomalies, which are lacking in Archean chemical sediments, the REE patterns of the central México groundwaters are also statistically similar to REE patterns of Archean chemical sediments, especially those of the 3.45 Ga Strelley Pool Chert. Consequently, we suggest that without additional information, it may be premature to unequivocally conclude that Archean chemical sediments record REE signatures of an Archean ocean.     

鄂尔多斯盆地延长组长7沉积期物源分析及母岩类型研究

通过对鄂尔多斯盆地延长组长7砂岩的类型、轻重矿物特征、重矿物聚类分析及泥岩的地化特征研究,并结合盆地周边源区露头剖面的岩性组合资料,讨论了长7沉积期的物源方向,恢复各源区母岩性质。经研究表明:鄂尔多斯盆地长7沉积期存在五个方向物源,东北、西南为主要的物源方向,西北、南部作为次要物源方向;其中东北源区母岩以中基性岩浆岩、高级变质岩为主,西南源区母岩以白云岩、浅变质岩为主,西北源区母岩以沉积岩为主,浅变质岩次之,南部源区母岩以含灰岩、碎屑岩为主,浅变质岩次之;另外经讨论证实西部存在局限的物源供给区,母岩主要为白云岩。     

Multistage dolomitization and distribution of dolomitized bodies in Early Jurassic carbonate platforms (Southern Alps,Italy)

The Early Jurassic dolomitized carbonates are a hydrocarbon exploration target in Northern Italy. Of these carbonates, the Liassic Albenza Formation platform and the overlying Sedrina Formation shelf were studied to define a pervasive dolomitization model and to shed light on dolomite distribution in the sub‐surface. Field work, as well as analyses of well cores, stable isotopes, trace elements and fluid inclusions, was carried out on the outcropping thrust belt and sub‐surface deformed foreland of the Southern Alps. Petrographic analyses showed a first, pervasive, replacement dolomitization phase (D1) followed by volumetrically less important dolomite cement precipitation phases (D2, D3 and D4). The δ¹⁸O values fall between ?8·2‰ and 0·1‰ Vienna‐Pee Dee Belemnite with the more depleted samples belonging to dolomite cement‐rich dolostones; the δ¹³C ranges from 2·6‰ to 3·7‰ Vienna‐Pee Dee Belemnite. Analysis of trace elements showed different Fe and Mn contents in the sub‐surface and outcropping dolostones, and a higher Fe in the younger dolomite cements. An increase in the precipitation temperature (up to 130 °C from fluid inclusion data) and a decrease in diagenetic fluid salinity (from sea water to brackish) are observed from the first pervasive replacement dolomite to the dolomite cement phases. Field observations indicate that, in the Albenza Formation, dolomitization was limited to palaeohighs or faulted platform margins in the Early Jurassic carbonates. The pervasive replacement phase is interpreted based on a ‘compaction model’; the formation fluids expelled from compacting basinal carbonates could have funnelled along faults into permeable palaeohighs. The high homogenization temperature of the dolomite cements and decreased salinities indicate precipitation at great depth with an influx of meteoric water. These data, along with the thermal history, suggest that the dolomite cements precipitated according to the ‘tectonic squeegee’ dolomitization model. The dolomite precipitation temperature was set against the thermal history of the carbonate platform to interpret the timing of dolomite precipitation. The dolomite precipitation temperatures (90 to 100 °C) were reached in the studied formations first in the thrust fold belt (Early Tertiary, 60 Ma), and then in the foreland succession during the Late Tertiary (10 Ma). This observation suggests that the dolomite precipitation fronts moved southwards over time, recording a ‘diagenetic wave’ linked to the migration of the orogenic system. Observations suggest that the porosity increased during the first phase of replacement dolomitization while the dolomite cementation phases partially occluded the pores. The distribution of porous dolomitized bodies is therefore linked to the ‘compaction dolomitization’ model.     

Aragonite and magnesite in eclogites from the Jæren nappe,SW Norway: disequilibrium in the system CaCO3–MgCO3 and petrological implications

Eclogites from the Jæren nappe in the Caledonian orogenic belt of SW Norway contain aragonite, magnesite and dolomite in quartz‐rich layers. The carbonates comprise composite grains that occur interstitially between phases of the eclogite facies assemblage: garnet + omphacite + zoisite + clinozoisite + quartz + apatite + rutile ± dolomite ± kyanite ± phengite. Pressure and temperature conditions for the main eclogite stage are estimated to be 2.3–2.8 GPa and 585–655 °C. Published ultrahigh pressure (UHP) experiments on CaO‐, MgO‐ and CO₂‐bearing systems have shown that equilibrium assemblages of aragonite and magnesite form as a result of dolomite breakdown at pressures >5 GPa. As a result, recognition of magnesite and aragonite in eclogite facies rocks has been used as an indicator for UHP conditions. However, petrological testing showed that the samples studied here have not experienced such conditions. Aragonite and magnesite show disequilibrium textures that indicate replacement of magnesite by aragonite. This process is inferred to have occurred via a coupled dissolution–precipitation reaction. The formation of aragonite is constrained to eclogite facies conditions, which implies that the studied rocks have experienced metasomatic, reactive fluid flow during their residence at high pressure (HP) conditions. During decompression, the bimineralic carbonate aggregates were overgrown by rims of dolomite, which partially reacted with aragonite to form Mg‐calcite. The well‐preserved carbonate assemblages and textures observed in the studied samples provide a detailed record of the reaction series that affected the rocks during and after their residence at P–T conditions near the coesite stability field. Recognition of the HP mechanism of magnesite replacement by aragonite provides new insight into metasomatic processes that occur in subduction zones and illustrates how fluids facilitate HP carbonate reactions that do not occur in dry systems at otherwise identical physiochemical conditions. This study documents that caution is warranted in interpreting aragonite‐magnesite associations in eclogite facies rocks as evidence for UHP metamorphic conditions.     

Pb-Pb age of Jatulian carbonate rocks: The Tulomozero Formation of southeast Karelia

The U-Pb systematics of 25 carbonate samples collected from the Upper Jatulian Tulomozero Formation in southeastern area of the Baltic shield has been studied. The U-Pb systems of Jatulian carbonates metamorphosed here under conditions of the greenschist facies likely have not been reset completely. Samples have been collected from core sections recovered by drilling 60 to 70 km apart from each other in western and eastern areas of the Onega Lake region. In majority, the rocks sampled characterize a thick upper member of the Tulomozero Formation, and a few samples have been collected in addition from its middle and lower members. The analyzed dolomitic rocks (Mg/Ca=0.60–0.68) have variable Mn (54–1450 ppm) and Sr (31–438 ppm) concentrations. Powdered dolomite samples have been treated preliminary in 1 N solution of ammonium acetate in order to get material for analysis enriched in pre-metamorphic carbonate phases in terms of U-Pb systematics. Five samples have been subjected to stepwise dissolution in 0.5 N HBr to analyze their carbonate phases L-1, L-2, L-3 and siliciclastic fraction for getting a deeper insight into the U-Pb systematics. The U-Pb characteristics of carbonate and siliciclastic fractions suggest deposition of studied carbonate sediments in two different paleobasins. In addition, they show for same samples the partial Pb redistribution between carbonate and siliciclastic components in the course of metamorphism and Pb gain from allogenic metamorphic fluids. The Pb-Pb date of 2090 ± 70 Ma (MSWD = 2.0) is estimated for the least altered dolomite samples from upper member of the Tulomozero Formation, which represent marine sediments of a paleobasin and contain a minimum of siliciclastic material, being the least-contaminated by gained Pb. The date obtained is well consistent with U-Pb and Sm-Nd ages established for the Jatulian volcanogenic rocks in northern and western areas of the Baltic shield.     

Microbenthic distribution of Proterozoic tidal flats: environmental and taphonomic considerations

Silicified carbonates of the late Mesoproterozoic to early Neoproterozoic Society Cliffs Formation, Baffin Island, contain distinctive microfabrics and microbenthic assemblages whose paleo-environmental distribution within the formation parallels the distribution of these elements through Proterozoic time. In the Society Cliffs Formation, restricted carbonates--including microdigitate stromatolites, laminated tufa, and tufted microbial mats--consist predominantly of synsedimentary cements; these facies and the cyanobacterial fossils they contain are common in Paleoproterozoic successions but rare in Neoproterozoic and younger rocks. Less restricted tidal-flat facies in the formation are composed of laminated microbialites dominated by micritic carbonate lithified early, yet demonstrably after compaction; these strata contain cyanobacteria that are characteristic in Neoproterozoic rocks. Within the formation, the facies-dependent distribution of microbial populations reflects both the style and timing of carbonate deposition because of the strong substrate specificity of benthic cyanobacteria. A reasonable conclusion is that secular changes in microbenthic assemblages through Proterozoic time reflect a decrease in the overall representation of rapidly lithified carbonate substrates in younger peritidal environments, as well as concomitant changes in the taphonomic window of silicification through which early life is observed.     

Origin and diagenetic evolution of Ca–Mg–Fe carbonates in some coalfields of Japan

Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca²⁺ and Mg²⁺ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks.     

Distribution of elements in coexisting minerals and the problem of chemical disequilibrium in metamorphosed basic rocks

Distribution of elements in coexisting minerals—biotite, hornblende, augite, hypersthene and plagioclase in charnockitic rocks of West Uusimaa Complex, Finland, is mostly orderly indicating a close approach to chemical equilibrium. The distribution of iron and magnesium in coexisting hornblende and pyroxenes of basic charnockites and other rocks of granulite facies from several different areas is also orderly but the variation in the fugacities of H₂O and H₂ may cause a disorderly distribution locally in some rocks. The probable oxidation or reduction reactions are discussed on the basis of thermochemical and mineralchemical data.     

Multi-stage metamorphism by progressive accretion of continental blocks,example from the Western Hindu Kush

Basement rocks from the Western Hindu Kush preserve evidence of multiple metamorphic and magmatic events that occurred along the boundary between the Archean–Proterozoic Afghan Central and Afghan–Tajik Blocks. To verify the different metamorphic stages or events, mineral textures and phase equilibria in metamorphic basement rocks and their age relations to magmatic episodes have been investigated. Quartzofeldspathic gneiss and migmatite with lenses of amphibolite (with assumed Proterozoic age for their metamorphism) are intruded by the Triassic Hindu Kush granitoid batholith and small Cretaceous and Oligocene granite intrusions. The age of thermal overprint (210–170 Ma) by the Triassic batholith is confirmed by new monazite data. Both Triassic and Cretaceous granitoids and surrounding basement rocks underwent subsequent metamorphism up to epidote–amphibolite facies. The degree of this metamorphism increases southward at the contact to the Kabul Block, which under-plates the Western Hindu Kush from the south. An early Miocene age was obtained by Pb–Th analyses in thorite and huttonite, which are close or slightly younger than the Oligocene granite in this area. The Cretaceous meta-granodiorite near the border with the Kabul Block contains xenoliths of granulite facies rocks that could come from the Neoarchean granulite facies basement of the Kabul Block. The multi-stage metamorphic and magmatic evolution classifies the Hindu Kush mountain belt as a long-lived suture zone that was active since the early Palaeozoic. The results of this study support the interpretation about possible relations of the Afghan Central Blocks to the southern margin of Eurasia during the evolution of Para- and Neotethys.