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1.
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2.
Conjoint consideration of distribution of major, rare earth elements (REE) and Y (combined to REY) and of H, O, C, S, Sr isotopes reveals that four types of groundwater are distinguishable by their chemical composition presented by spider patterns. REY patterns indicate thermo-saline deep water and two types of shallow saline groundwaters. Presence of connate waters is not detectable. Sr isotope ratios distinguish three sources of Sr: fast and slow weathering of biotite and K-feldspar in Pleistocene sediments, respectively, and dissolution of limestones. δ13C(DIC) indicate dissolution of limestone under closed and open system conditions. Numerous samples show δ13C(DIC) > 13‰ which is probably caused by incongruent dissolution of calcite and dolomite. The brines from below 1,000 m represent mixtures of pre-Pleistocene seawater or its evaporation brines and infiltrated post-Pleistocene precipitation. The shallow waters represent mixtures of Pleistocene and Recent precipitation salinized by dissolution of evaporites or by mixing with ascending brines. The distribution of water types is independent on geologic units and lithologies. Even the Tertiary Rupelian aquiclude does not prevent salinization of the upper aquifer.  相似文献   

3.
Mesoproterozoic (∼ 1600 Ma old) Salkhan Limestone (Semri Group) of the Vindhyan Supergroup, exposed in Rohtas district of Bihar, India, preserves an abundant and varied ancient microbial assemblage. These microfossils are recorded in three distinctly occurring cherts viz., bedded chert, stromatolitic chert and cherty stromatolites. 27 morphoforms belonging to 14 genera and 21 species have been recognized. Six unnamed forms are also described. The microbial assemblage, almost exclusively composed of the remnants of cyanobacteria, is dominated by entophysalidacean members and short trichomes and can be termed as ‘typical Mesoproterozoic microbiotas’. The assemblage includes characteristic mat-forming scytonematacean and entophysalidacean cyanobacteria.Eoentophysalis is the dominant organism in the assemblage. Ellipsoidal akinetes of nostocalean cyanobacteria(Archaeollipsoides) and spherical unicells also occur; both are distinct from mat forming assemblage, allochthonous and possibly planktic. Co-occurrence of the microbiotas and precipitates is related to the depositional environment of the Mesoproterozoic tidal flats with high carbonate saturation.  相似文献   

4.
Strontium isotopic composition (87Sr/86Sr) of two petrographically, chemically and isotopically (δ18O and δ13C) distinct phases of burial calcites from the Lincolnshire Limestone are indistinguishable (0.70820± 26). The mean 87Sr/86Sr ratio of these phases is considerably more radiogenic than 87Sr/86Sr ratios of Bajocian marine waters (～0.70725). Neither Bajocian marine waters nor meteoric waters buffered by host marine carbonate in the Limestone could have precipitated the burial spars. Radiogenic strontium may have been contributed from K-feldspar dissolution and/or clay recrystallization, either within clastic portions of the Limestone itself, or from major clastic units adjacent to the Limestone. Alternatively, Palaeozoic marine waters or remobilized Palaeozoic marine carbonate and/or sulphate could have supplied the necessary radiogenic strontium.  相似文献   

5.
Remarkable bedding features occur in Middle Cambrian platy limestone of the Western Hills close to Beijing in NE-China, which are intercalated in a sequence of shallow water carbonates (mudstones, storm deposits, oolitic grainstones). The platy limestone beds (up to 5 cm thickness) have undergone complex diagenetic compaction and pressure solution. Varying facies types are characterized by wavy, stylolitic boundaries with different thickness of clay accumulation and common lateral pinch out. Cross-cutting relationships of stylolites commonly destroy primary bed-surfaces. This indicates an intimate interfingering resulting in an indenting fabric of primary separated facies types. Nevertheless, primary sedimentary boundaries can be recognized. There occur varying types of compaction features documented by different stylolite types with varying amplitudes and thickness of clay-enrichments (parallel clay seams, stylolamination, stylo-nodular and stylo-brecciated structures with multi-grained seams). Bedded limestone of the type documented, generally belong to the limestone family of Plattenkalk, Lithographic Limestone or platy limestone, which can form in different environments. Consequently, using these names without detailed data on some specific parameters (e.g. thickness, surface morphology, composition of allochems, particle and crystal size) results in more confusion and hinders the comparison of Plattenkalk, Lithographic Limestone and platy limestone from different locations throughout the earth history. Therefore, a classification is proposed here which is based on macroscopic, microscopic, and sub-microscopic parameters. Plattenkalk and platy limestone are considered to form the two main groups. Plattenkalk beds are laterally consistent and have parallel, horizontal surfaces. Platy limestone can pinch out laterally and reveals irregular and inclined bed surfaces. Single beds in both can have different thickness, internal structure (e.g. micritic, microsparitic) and fabric (e.g. homogeneous, nodular), particle content and other variations (e.g. chemical, mineralogical). These parameters should be added to the basic name and used in a system similar to Folk’s limestone classification. Lithographic Limestone is defined as a subgroup of Plattenkalk with well-defined parameters. A consequent use of this classification will also help to understand fossil preservation and/or non-preservation in different types of Plattenkalk, Lithographic Limestone, and platy limestone.  相似文献   

6.
Stable and radiogenic isotope composition of stratiform Cu–Co–Zn mineralization and associated sedimentary rocks within the Boléo district of the Miocene Santa Rosalía basin, Baja California Sur, constrains the evolution of seawater and hydrothermal fluids and the mechanisms responsible for sulfide and oxide deposition. Stable isotope geochemistry of limestone and evaporite units indicates a strong paleogeographic influence on the chemistry of the water column. Near-shore limestone at the base of the Boléo Formation is characterized by modified marine carbon (δ 13CPDB=−6.0 to +4.4‰) and oxygen (δ 18OSMOW=+19.5 to +26.2‰) isotope composition due to the influx of 13C- and 18O-depleted fluvial water. Sulfate sulfur isotope composition (δ 34SCDT=+17.21 to +22.3‰ and δ 18OSMOW=+10.7 to +13.1‰) for basal evaporite and claystone facies are similar to Miocene seawater. Strontium isotopes are less radiogenic than expected for Miocene seawater due to interaction with volcanic rocks. Low S/C ratios, high Mn contents and sedimentological evidence indicate the basin water column was oxidizing. The oxygenated basin restricted sulfide precipitation to within the sedimentary pile by replacement of early diagenetic framboidal pyrite and pore-space filling by Cu–Co–Zn sulfides to produce disseminated sulfides. Quartz–Mn oxide oxygen isotope geothermometry constrains mineralization temperature between 18 and 118°C. Sulfur isotopes indicate the following sources of sulfide: (1) bacterial sulfate reduction within the sedimentary pile produced negative δ 34S values (<−20‰) in framboidal pyrite; and (2) bacterial sulfate reduction at high temperature (80–118°C) within the sedimentary pile during the infiltration of the metal-bearing brines produced Cu–Co–Zn sulfides with negative, but close to 0‰, δ 34S values. Isotope modeling of fluid-rock reaction and fluid mixing indicates: (1) sedimentary and marine carbonates (δ 13C=−11.6 to −3.2‰ and δ 18O=+19.0 to +21.8‰) precipitated from basin seawater/pore water that variably mixed with isotopically depleted meteoric waters; and (2) hydrothermal calcite (δ 13C=−7.9 to +4.3‰ and δ 18O=+22.1 to +25.8‰) formed by dissolution and replacement of authigenic marine calcite by downward-infiltrating metalliferous brine and brine-sediment exchange, that prior to reaction with calcite, had mixed with isotopically depleted pore water. The downward infiltration of metalliferous brine is inferred from lateral and stratigraphic metal distributions and from the concentration of Cu sulfides along the upper contact of pyrite-bearing laminae. The co-existence and textural relationships among framboidal pyrite, base metal sulfides, carbonate and Mn–Fe oxides (including magnetite) within mineralized units are consistent with carbonate replacement and high-temperature bacterial reduction within the sedimentary pile occurring simultaneously below a seawater column under predominantly oxygenated conditions.  相似文献   

7.
The early Pliocene Shirahama Limestone is a grainstone-packstone principally composed of fragments of algae, bryozoa, and echinoderm and subordinate volcanic rocks. The limestone was variously dolomitized and the regional distribution of dolomite is patchy. Dolomite occurs as isolated crystals filling pores, moulds, and solution vugs, and mosaic aggregates replacing bioclasts. Calcite occurs as rim and pore-filling sparry cements, and as calcareous skeletons. Isotopically, the dolomites are classified into a heavy oxygen group (?2 to ? 3.5%0 PDB) and a light oxygen group (?5.5 to ? 7.5%0 PDB). Calcite associated with heavy oxygen dolomite has δ18O of ? 6.5 to ?8.5%0 PDB, whereas those associated with light oxygen dolomite have a wide range from ?7.5 to ?14%0 PDB. Calcite in dolomite-free limestone has an oxygen isotopic composition of ?2 to ?8.5%0 PDB. Textures, chemistry, and isotopic evidence indicate that heavy oxygen calcite formed in freshwater, and heavy oxygen dolomite in a meteoric-marine mixture of 10–30% seawater. Light oxygen calcite and dolomite precipitated from modified hydrothermal fluids at approximately 30–65°C. Petrographic features, and both isotopic and chemical evidence suggest that the Shirahama Limestone was exposed to freshwater soon after deposition. Subsequently blocky calcite precipitated (Stage I). The limestone was locally submerged in the meteoric-marine mixture due to gradual subsidence or eustatic movement. This led to the precipitation of heavy oxygen, zoned dolomite and dolospar (Stage II). Hydrothermal alterations occurred in the area a few Myr ago, and related hydrothermal fluids and mixed meteoric-hydrothermal waters caused dedolomitization of some zoned dolomite, partial dissolution of vuggy dolomite, precipitation of limpid dolomite and recrystallization of some earlier dolomites (Stage III). Zeolites were also precipitated from these fluids. Finally, the Shirahama Limestone was exposed again to freshwater and sparry calcite precipitated to plug some of the remaining pores (Stage IV).  相似文献   

8.
The Raipur Group of the Chattisgarh Basin preserves two major Late Mesoproterozoic carbonate platforms. The lower platform is about 490-m thick, separated from the upper platform (~ 670 m thick) by a 500-m thick calcareous shale. Carbonate strata cover almost 40% of the Chattisgarh Basin outcrop and represent two major platform types: a) a non-stromatolitic ramp (the Charmuria/Sarangarh Limestone) and b) a platform developed chiefly in the intertidal to shallow subtidal environment with prolific growth of stromatolites (the Chandi/Saradih Limestone). The first platform consists primarily of the black Timarlaga limestone that is locally replaced by early diagenetic dolomite. This carbonate platform experienced strong storm waves and was subsequently drowned by a major transgression, during which extensive black limestone–marl rhythmite was deposited, followed by deposition of the Gunderdehi Shale. The carbonate factory was later re-established with development of an extensive stromatolite-dominated Charmuria/Sarangarh platform that ranged from restricted embayment to open-marine conditions. Sea-level change played a major role in controlling the broad facies pattern and platform evolution. The δ13C signatures of the Chattisgarh limestones, falling within a relatively narrow range (0 to + 4‰) are typical for Upper Mesoproterozoic carbonate rocks. δ18O values, however, have a greater range (− 5.7 to − 13.3‰) indicating significant diagenetic alteration of some samples. Likely dysoxic or anoxic conditions prevailed during deposition of the black Timarlaga limestone and well-oxygenated conditions during deposition of the Gunderdehi Shale and Saradih/Chandi stromatolite. The lack of 17β,21α (moretanes) and high Tmax values suggest mature organic matter in the non-stromatolitic ramp. A paucity of diagnostic eukaryotic steroids indicates that algae were rare in the Chattisgarh Basin. A high content of hopanes supports a generally bacterially-dominated Proterozoic ocean in which various stromatolites flourished.  相似文献   

9.
平顶山煤田的太原组属于混合型的碳酸盐浅海和陆源碎屑海岸沉积。下部和上部灰岩段主要形成于滨海潮间带和浅海中,并在其中发育行风暴浊流沉积。中部碎屑岩段为障壁岛-泻湖-潮坪体系沉积。太原组煤的显微组分为微镜惰煤,煤质属于低灰高硫煤。  相似文献   

10.
The strata-bound Cu−Pb−Zn polymetallic sulfide deposits occur in metamorphic rocks of greenschist phase of the middle-upper Proterozoic Langshan Group in central Inner Mongolia. δ34S values for sulfides range from −3.1‰ to +37.3‰, and an apparent difference is noticed between vein sulfides and those in bedded rocks. For example, δ34S values for bedded pyrite range from +10.6‰ to +20.0‰, while those for vein pyrite vary from −3.1‰ to +14.1‰. δ34S of bedded pyrrhotite is in the range +7.9‰–+23.5‰ in comparison with +6.5‰–+17.1‰ for vein pyrrhotite. The wide scatter of δ34S and the enrichment of heavier sulfur indicate that sulfur may have been derived from H2S as a result of bacterial reduction of sulfates in the sea water. Sulfur isotopic composition also differs from deposit to deposit in this area because of the difference in environment in which they were formed. The mobilization of bedded sulfides in response to regional metamorphism and magmatic intrusion led to the formation of vein sulfides. δ18O and δ13C of ore-bearing rocks and wall rocks are within the range typical of ordinary marine facies, with the exception of lower values for ore-bearing marble at Huogeqi probably due to diopsidization and tremalitization of carbonate rocks. Pb isotopic composition is relatively stable and characterized by lower radio-genetic lead. The age of basement rocks was calculated to be about 23.9 Ma and ore-forming age 7.8 Ma.207Pb/204Pb−206Pb/204Pb and208Pb/204Pb−206Pb/204Pb plots indicate that Pb may probably be derived from the lower crust or upper mantle. It is believed that the deposits in this region are related to submarine volcanic exhalation superimposed by later regional metamorphism and magmatic intrusion.  相似文献   

11.
The Tono sandstone-type uranium mine area, middle Honsyu, Japan is composed of Miocene lacustrine sedimentary rocks in the lower part (18–22 Ma) and marine facies in the upper part (15–16 Ma). Calcite and pyrite occur as dominant diagenetic alteration products in these Neogene sedimentary rocks. The characteristics of calcite and pyrite differ significantly between lacustrine and marine facies. Abundant pyrite, calcite, organic matter, and small amounts of marcasite or pyrrhotite occur in the lacustrine facies, whereas small amounts of calcite and framboidal pyrite, organic matter and no marcasite or pyrrhotite are found within the marine units. The δ13C values of calcite in the lacustrine deposits are low (−19 to −6‰ PDB) but those in marine formation are high (−11 to +3‰). This implies that the contribution of marine carbonate is larger in upper marine sedimentary rocks, and carbon in calcite in the lower lacustrine formation was derived both from oxidation of organic matter and from dissolved marine inorganic carbon. The δ34S values of framboidal pyrite in the upper marine formation are low (−14 to −8‰ CDT), indicating a small extent of bacterial seawater sulfate reduction, whereas those of euhedral-subhedral pyrite in the lower lignite-bearing arkose sandstone are high (+10 to +43‰), implying a large extent of closed-system bacterial seawater sulfate reduction. The δ34S and δ13C data which deviate from a negative correlation line toward higher δ13C values suggest methanogenic CO2 production. During diagenesis of the lacustrine unit, large amounts of euhedral-subhedral pyrite were formed, facilitated by extensive bacterial reduction of seawater sulfate with concomitant oxidation of organic matter, and by hydrolysis reactions of organic matter, producing CH4 and CO2. Uranium minerals (coffinite and uraninite) were also formed at this stage by the reduction of U6+ to U4+. The conditions of diagenetic alteration within the lacustrine deposits and uranium mineralization is characterized by low Eh in which nearly equal concentrations of CH4 and HCO3 − existed and reduced sulfur species (H2S, HS−) are predominant among aqueous sulfur species, whereas diagenetic alteration of the marine formations was characterized by a predominance of SO4 2− among dissolved sulfur species. Modern groundwater in the lacustrine formation has a low Eh value (−335 mV). Estimated and measured low Eh values of modern and ancient interstitial waters in lacustrine environments indicate that a reducing environment in which U4+ is stable has been maintained since precipitation of uranium minerals. Received: 9 February 1996 / Accepted: 11 April 1997  相似文献   

12.
Enriched13C/12C ratios with δ13C ∼3%0 (w.r.t PDB) of two Late Riphean (∼ 700-610 Ma) intracratonic carbonate successions viz., Bhander Limestone of Vindhyan Basin and Raipur Limestone of Chattisgarh Basin suggest higher organic productivity during this period. This view is supported by sedimentological evidence of higher biohermal growth and consequent increase in depositional relief in the low gradient ramp settings inferred for these basins. Oxygen isotope analysis of these carbonates show distinct segregation between enriched deeper water carbonate mudstone and depleted shallow water stromatolite facies that received fresh water influx. This shows that facies-specific analyses can be useful in understanding the depositional setting of these sediments.  相似文献   

13.
山西柳林成家庄剖面太原组发育7层灰岩,从下到上依次为半沟灰岩、吴家峪灰岩、庙沟灰岩、下毛儿沟灰岩、上毛儿沟灰岩、斜道灰岩和东大窑灰岩。通过详细的野外观测和室内镜下薄片研究,确定了各层灰岩的沉积相类型,恢复了当时的沉积环境和各层灰岩沉积时相对水体深度的变化。其中庙沟灰岩属中缓坡相沉积,吴家峪灰岩、下毛儿沟灰岩、上毛儿沟灰岩、斜道灰岩和东大窑灰岩均属浅缓坡相沉积,半沟灰岩属后缓坡相沉积。7层灰岩的相对水体深度关系为:庙沟灰岩>斜道灰岩>东大窑灰岩>下毛儿沟灰岩>上毛儿沟灰岩>吴家峪灰岩>半沟灰岩。在太原组内识别出6次沉积间断、7次小型沉积旋回,总体构成2次明显的相对海平面升降旋回。  相似文献   

14.
Bulk carbonate samples of hemipelagic limestone–marl alternations from the Middle and Upper Triassic of Italy are analysed for their isotopic compositions. Middle Triassic samples are representative of the Livinallongo Formation of the Dolomites, while Upper Triassic hemipelagites were sampled in the Pignola 2 section, within the Calcari con Selce Formation of the Southern Apennines in Southern Italy. Triassic hemipelagites occur either as nodular limestones with chert nodules or as plane‐bedded limestone–marl alternations which are locally silicified. In the Middle Triassic Livinallongo Formation, diagenetic alteration primarily affected the stable isotopic composition of sediment surrounding carbonate nodules, whereas the latter show almost pristine compositions. Diagenesis lowered the carbon and oxygen isotope values of bulk carbonate and introduced a strong correlation between δ13C and δ18O values. In the Middle Triassic successions of the Dolomites, bulk carbonate of nodular limestone facies is most commonly unaltered, whereas carbonate of the plane‐bedded facies is uniformly affected by diagenetic alteration. In contrast to carbonate nodules, plane‐bedded facies often show compaction features. Although both types of pelagic carbonate rocks show very similar petrographic characteristics, scanning electron microscopy studies reveal that nodular limestone consists of micrite (< 5 μm in diameter), whereas samples of the plane‐bedded facies are composed of calcite crystals ca 10 μm in size showing pitted, polished surfaces. These observations suggest that nodular and plane‐bedded facies underwent different diagenetic pathways determined by the prevailing mineralogy of the precursor sediment, i.e. probably high‐Mg calcite in the nodular facies and aragonite in the case of the plane‐bedded facies. Similar to Middle Triassic nodular facies, Upper Triassic nodular limestones of the Lagonegro Basin are also characterized by uncorrelated δ13C and δ18O values and exhibit small, less than 5 μm size, crystals. The alternation of calcitic and aragonitic precursors in the Middle Triassic of the Dolomites is thought to mirror rapid changes in the type of carbonate production of adjacent platforms. Bioturbation and dissolution of metastable carbonate grains played a key role during early lithification of nodular limestone beds, whereby early stabilization recorded the carbon isotopic composition of sea water. The bulk carbonate δ13C values of Middle and Upper Triassic hemipelagites from Italy agree with those of Tethyan low‐Mg calcite shells of articulate brachiopods, confirming that Triassic hemipelagites retained the primary carbon isotopic composition of the bottom sea water. A trend of increasing δ13C from the Late Anisian to the Early Carnian, partly seen in the data set presented here, is also recognized in successions from tropical palaeolatitudes elsewhere. The carbon isotopic composition of Middle and Upper Triassic nodular hemipelagic limestones can thus be used for chemostratigraphic correlation and palaeoenvironmental studies.  相似文献   

15.
《Sedimentary Geology》1999,123(1-2):9-29
Sedimentological, biostratigraphic and magnetostratigraphic studies were carried out on five Late Eocene–Early Oligocene profiles in the Buda Hills, Hungary. The Szépvölgy Limestone Formation accumulated on the pre-Eocene basement. Basal strata of the limestone consist of a thin conglomerate followed by a coralgal limestone. The overlying limestone contains abundant Nummulites, Discocyclina. The contact between these two members is sharp. The Szépvölgy Limestone body, covering 60–65 km2, is considered a carbonate bank. Above the limestone, the siliciclastic slope deposits of the pelagic and turbiditic Buda Marl, and the euxinic Tard Clay accumulated. A huge multiphase hydrothermal cave system developed in the Szépvölgy Limestone resulting in a long-term composite palaeokarstic evolution lasting from the Late Eocene to the Quaternary. The first palaeokarst phase during the Late Eocene is represented by two generations of early marine cavity filling sediments of caymanite-type, deposited at sea-level. The earlier, carbonate infilling is conformable while the younger, siliciclastic one is disconformable with the bedding of the host rock. Bio- and magnetostratigraphic studies indicate that deposition of the caymanites-bearing palaeokarst host sequence started in the Late Eocene, during Chron C15r (35.3 Ma) and terminated in the Early Oligocene during Chron C13n (33 Ma). Two marker horizons are present, the first is between the Szépvölgy Limestone and Buda Marl at ∼34.6 Ma, and the second horizon is between the Buda Marl and the Tard Clay at 33.5 Ma. The Szépvölgy Limestone, deposited on a mobile shelf, represents a deepening upward sequence, interrupted by two lowstand events. They can be correlated with the PHd event of Keller et al., 1987 (Global distribution of late Palaeogene hiatuses. Geology 15, 199–203) and resulted in marine palaeokarstification. The carbonate shelf with the infillings drowned at 34.6 Ma. The caymanites accumulated at about 35.2–35.0 Ma and represent short-term palaeokarstic events. Their deposition record was estimated in several thousand years.  相似文献   

16.
The Pennsylvanian phylloid algal mounds exposed in the Cervatina Limestone of the Cantabrian Zone (NW Spain) developed during the highstands of high-frequency shallowing-upward cycles and lack evidence of subaerial exposure at their tops. Mound core facies are composed of massive bafflestones with variable amounts of calcite cements and anchicodiacean phylloid algae with cyathiform thalli preserved in growth position. Through standard petrographic, isotopic (δ18O and δ13C), major and trace element (Ca, Mg, Fe, Mn, Sr) and cathodoluminescence analyses, five calcite cement phases (cement 1 (C1)–cement 5 (C5)) have been identified filling primary and secondary pores. Early marine diagenesis is represented by micritization and non-luminescent to mottled-dull luminescent high-Mg calcite fibrous marine cement (C1). A dissolution phase then occurred and created vuggy and moldic pores. Based on the absence of field or petrographical or geochemical evidence of exposure, it is inferred that dissolution occurred in near-surface undersaturated marine waters with respect to aragonite related to progressive organic matter oxidation. Secondary porosity was subsequently filled by dull-bright-dull bladed high-Mg calcite (C2), which precipitated in the early shallow burial from marine-derived pore waters. Remaining porosity was occluded by shallow-burial precipitates consisting of non-luminescent scalenohedral low-Mg calcite (C3) followed by non-ferroan dull luminescent calcite spar (C4). Latter phases of calcite spar exhibiting non- and dull luminescence (C5) are associated with burial calcite veins. Low δ18O values (around ?8‰), moderately depleted δ13C values (around 0.5‰) and the homogeneity of trace element contents of carbonate matrix, cements and vein-filling calcites suggest burial isotopic re-equilibration and recrystallization, probably in Early Permian times during post-thrusting orocline formation.  相似文献   

17.
Hypersthene-garnet-sillimanite-quartz enclaves were studied in orthopyroxene-plagioclase and orthopyroxene-clinopyroxene crystalline schists and gneisses from shear zones exposed in Palenyi Island in the Early Proterozoic Belomorian Mobile Belt. Qualitative analysis of mineral assemblages indicates that these rocks were metamorphosed to the granulite facies (approximately 900°C and 10–11 kbar). Oxygen isotopic composition was determined in rock-forming minerals composing zones of the enclaves of various mineralogical and chemical composition. The closure temperatures of the isotopic systems obtained by methods of oxygen isotopic thermometry are close to the values obtained with mineralogical geothermometers (Grt-Opx and Grt-Bt) and correspond to the high-temperature granulite facies (860–900°C). Identified systematic variations in the δ18O values were determined in the same minerals from zones of different mineral composition. Inasmuch as these zones are practically in contact with one another, these variations in δ18O cannot be explained by the primary isotopic heterogeneity of the protolith. The model calculations of the extent and trend of the δ18O variations in minerals suggest that the only mechanism able to generate the zoning was fluid-rock interaction at various integral fluid/rock ratios in discrete zones. This demonstrates that a focused fluid flux could occur in lower crustal shear zones. The preservation of high-temperature isotopic equilibria of minerals testifies that the episode of fluid activity at the peak of metamorphism was very brief.  相似文献   

18.
The isotopic composition of dissolved boron, in combination with the elemental concentrations of B, Cl and salinities in freshwater-seawater mixed samples taken from the estuary of the Changjiang River, the largest one in China, was investigated in detail in this study. Brackish water and seawater samples from the estuary of the Changjiang River were collected during low water season in November, 1998. Boron isotopic compositions were determined by the Cs2BO^＋2-graphite technique with a analytical uncertainty of 0.2‰ for NIST SRM 951 and an average analytical uncertainty of 0.8‰ for the samples. The isotopic compositions of boron, expressed in δ^11B, and boron concentrations in the Changjiang River at Nanjing and seawater from the open marine East Sea, China, are characterized by δ^11B values of -5.4‰ and 40.0‰, as well as 0.0272 and 4.43 mg B/L, respectively. Well-defined correlations between δ^11B values, B concentrations and Cl concentrations are interpreted in terms of binary mixing between fiver input water and East Sea seawater by a process of straightforward dilution. The offsets of δ^11B values are not related to the contents of clastic sediment and to the addition of boron. These relationships favor a conservative behavior of boron at the estuarine of the Changjiang River.  相似文献   

19.
《Gondwana Research》2001,4(3):387-394
The rocks of Marwar Supergroup in the trans-Aravalli sector in western India are presumed to span the time interval between Neoproterozoic and early Cambrian. This, predominantly unfossiliferous, marine sedimentary sequence is characterized by a lower arenaceous facies (Jodhpur Group), middle carbonate facies (Bilara Group) and upper argillaceous— arenaceous facies (Nagaur Group) rocks. The sedimentation has been essentially in a shallow basin, described either as the fore-land slope of the rising Aravalli mountains or a sag-basin which developed and evolved due to subsidence of the updomed crust during Neoproterozoic Malani magmatism that failed to open rifts. The carbon isotopic profile for the Bilara Group carbonate rocks in the lower part shows marked oscillations and broadly negative δ13C character with negative anomalies as low as <−4.3‰PDB, observed near the base of Dhanapa Formation (lower unit) and <−6.5‰PDB in the overlying Gotan Formation (middle unit). The upper part of the profile shows a gradual positive shift. The carbon isotopic signatures of the Bilara Group rocks can be correlated with the end-Neoproterozoic — early Cambrian (Vendian — Tommotian) carbon isotopic evolution curve. Extremely low δ13C values indicate the glaciation related cold climatic postulates of the end-Neoproterozoic, followed by the warmer climatic conditions as indicated by the positive shift. The carbon isotopic data for Gotan Formation carbonates, at variance with the globally observed δ13C trends for early Tertiary, do not support the recently proposed Tertiary age for the Bilara Group.  相似文献   

20.
Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.  相似文献   

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