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1.
The Tepearasi Formation of the autochthonous Geyikdagi Group in the Central Tauride Belt, SE of Beysehir, is Dogger in age and consists dominantly of massive limestones and greyish dolomites occurring within the middle to upper sections. The total thickness of the dolomitic levels ranges from 100-300 m and laterally extends 500-700 m. Three types of dolomite were distinguished through petrographic analyses: homogeneous, mottled (saddle-crystalline) and joint-filling dolomite, which were interpreted to have formed in two different stages, early diagenetic and late diagenetic. The homogeneous dolomite of the early diagenetic stage is light-coloured and monotonous-textured and shows the form of a dolosparite mosaic. The mottled dolomite formed in the late diagenetic stage is light- to dark-coloured and coarsely granular idiomorphic. The other type of late diagenetic dolomite, described as the joint-filling type, presents a crystal growth pattern from the joint walls towards the centre of the joint space. I  相似文献   

2.
This paper describes the occurrence of dolomite and the mechanism of dolomitization of the Upper Triassic-Lower Jurassic K?z?loren Formation in the autochthonous Bolkardag? unit of the middle Taurus Mountains in south western Turkey. Dolomites were analyzed for geochemical, isotopic and crystallographic variation. Dolomites occur as a replacement of precursor carbonate and cement. The dolomite crystals range from <10 to ~1000 μm existing as both replacements and cements. Sr concentrations range between 84 and 156 ppm, and the molar Sr/Ca ratios of dolomitizing fluids are estimated to range between 0.0066 to 0.013 ratios. Dolomites are Ca-rich (with average CaCO3 and MgCO3 equal to 56.43 and 43.57 mol%, respectively) and they are non-stoichiometric, with an average Sr=116 ppm, Na=286 ppm, Mn=81 ppm, Fe=1329 ppm, and δ18O and δ13C ranges from –0.6‰ to –6.1‰ Pee Dee Belemnite [PDB], and +1.2 to +3.9‰ PDB. The North American Shale Composition [NASC]-normalized rare earth element (REE) values of the both limestone and dolomite sample groups show very similar REE patterns characterized by small positive Eu (mean=1.32 and mean=1.42, respectively) and slightly or considerably negative Ce (mean=0.61 and mean=0.72, respectively) anomalies and a clear depletion in all REE species. The K?z?loren Formation dolomites have been formed as early diagenetic from mixing zone fluids at the tidal-subtidal environment and at the late diagenetic from basinal brines at the shallow-deep burial depths.  相似文献   

3.
Dolomites from the upper calcareous-siliceous member of the Miocene Monterey Formation exposed west of Santa Barbara, California, were analysed for geochemical, isotopic and crystallographic variation. The data clearly document the progressive recrystallization of dolomite during burial diagenesis in marine pore fluids. Recrystallization is recognized by the following compositional and crystallographic variations. Dolomites have decreasing δ18O and δ13C compositions, decreasing Sr contents and increasing Mg contents with increasing burial depths and temperatures from east to west in the study area. δ18O values vary from 5·3‰ in the east to − 5·5‰ PDB in the west and are interpreted to reflect the greater extent and higher temperature of dolomite recrystallization in the west. δ13C values correlate with δ18O and decrease from 13·6‰ in the east to − 8·7‰ PDB in the west. Sr concentrations correlate positively with δ18O values and decrease from a mean of 750 ppm in the east to a mean of 250 ppm in the west. Mol% MgCO3 values inversely correlate with δ18O values and increase from a minimum of 41·0 in the east to a maximum of 51·4 in the west. Rietveld refinements of powder X-ray diffraction data indicate that the more recrystallized dolomites have more contracted unit cells and increased cation ordering. The fraction of the Ca sites in the dolomites that are occupied by Ca atoms increases slightly with the approach to stoichiometry. The fraction of the Mg sites occupied by Mg atoms strongly correlates with mol% MgCO3. Even in early diagenetic, non-stoichiometric dolomites, there is little substitution of Mg in Ca sites. During recrystallization, the amount of Mg substituting for Ca in Ca sites decreases even further. Most of the disorder in the least recrystallized, non-stoichiometric dolomites is related to substitution of excess Ca on Mg sites.  相似文献   

4.
Pervasive dolomites occur preferentially in the stromatoporoid biostromal (or reefal) facies in the basal Devonian (Givetian) carbonate rocks in the Guilin area, South China. The amount of dolomites, however, decreases sharply in the overlying Frasnian carbonate rocks. Dolostones are dominated by replacement dolomites with minor dolomite cements. Replacement dolomites include: (1) fine to medium, planar‐e floating dolomite rhombs (Rd1); (2) medium to coarse, planar‐s patchy/mosaic dolomites (Rd2); and (3) medium to very coarse non‐planar anhedral mosaic dolomites (Rd3). They post‐date early submarine cements and overlap with stylolites. Two types of dolomite cements were identified: planar coarse euhedral dolomite cements (Cd1) and non‐planar (saddle) dolomite cements (Cd2); they post‐date replacement dolomites and predate late‐stage calcite cements that line mouldic vugs and fractures. The replacement dolomites have δ18O values from ?13·7 to ?9·7‰ VPDB, δ13C values from ?2·7 to + 1·5‰ VPDB and 87Sr/86Sr ratios from 0·7082 to 0·7114. Fluid inclusion data of Rd3 dolomites yield homogenization temperatures (Th) of 136–149 °C and salinities of 7·2–11·2 wt% NaCl equivalent. These data suggest that the replacive dolomitization could have occurred from slightly modified sea water and/or saline basinal fluids at relatively high temperatures, probably related to hydrothermal activities during the latest Givetian–middle Fammenian and Early Carboniferous times. Compared with replacement dolomites, Cd2 cements yield lower δ18O values (?14·2 to ?9·3‰ VPDB), lower δ13C values (?3·0 to ?0·7‰ VPDB), higher 87Sr/86Sr ratios (≈ 0·7100) and higher Th values (171–209 °C), which correspond to trapping temperatures (Tr) between 260 and 300 °C after pressure corrections. These data suggest that the dolomite cements precipitated from higher temperature hydrothermal fluids, derived from underlying siliciclastic deposits, and were associated with more intense hydrothermal events during Permian–Early Triassic time, when the host dolostones were deeply buried. The petrographic similarities between some replacement dolomites and Cd2 dolomite cements and the partial overlap in 87Sr/86Sr and δ18O values suggest neomorphism of early formed replacement dolomites that were exposed to later dolomitizing fluids. However, the dolomitization was finally stopped through invasion of meteoric water as a result of basin uplift induced by the Indosinian Orogeny from the early Middle Triassic, as indicated by the decrease in salinities in the dolomite cements in veins (5·1–0·4 wt% NaCl equivalent). Calcite cements generally yield the lowest δ18O values (?18·5 to ?14·3‰ VPDB), variable δ13C values (?11·3 to ?1·2‰ VPDB) and high Th values (145–170 °C) and low salinities (0–0·2 wt% NaCl equivalent), indicating an origin of high‐temperature, dilute fluids recharged by meteoric water in the course of basin uplift during the Indosinian Orogeny. Faults were probably important conduits that channelled dolomitizing fluids from the deeply buried siliciclastic sediments into the basal carbonates, leading to intense dolomitization (i.e. Rd3, Cd1 and Cd2).  相似文献   

5.
Late Cambrian to Early Ordovician sedimentary rocks in the western Tarim Basin, Northwest China, are composed of shallow-marine platform carbonates. The Keping Uplift is located in the northwest region of this basin. On the basis of petrographic and geochemical features, four matrix replacement dolomites and one type of cement dolomite are identified. Matrix replacement dolomites include (1) micritic dolomites (MD1); (2) fine–coarse euhedral floating dolomites (MD2); (3) fine–coarse euhedral dolomites (MD3); and (4) medium–very coarse anhedral mosaic dolomites (MD4). Dolomite cement occurs in minor amounts as coarse saddle dolomite cement (CD1) that mostly fills vugs and fractures in the matrix dolomites. These matrix dolomites have δ18O values of ?9.7‰ to ?3.0‰ VPDB (Vienna Pee Dee Belemnite); δ13C values of ?0.8‰ to 3.5‰ VPDB; 87Sr/86Sr ratios of 0.708516 to 0.709643; Sr concentrations of 50 to 257 ppm; Fe contents of 425 to 16878 ppm; and Mn contents of 28 to 144 ppm. Petrographic and geochemical data suggest that the matrix replacement dolomites were likely formed by normal and evaporative seawater in early stages prior to chemical compaction at shallow burial depths. Compared with matrix dolomites, dolomite cement yields lower δ18O values (?12.9‰ to ?9.1‰ VPDB); slightly lower δ13C values (?1.6‰–0.6‰ VPDB); higher 87Sr/86Sr ratios (0.709165–0.709764); and high homogenization temperature (Th) values (98°C–225°C) and salinities (6 wt%–24 wt% NaCl equivalent). Limited data from dolomite cement shows a low Sr concentration (58.6 ppm) and high Fe and Mn contents (1233 and 1250 ppm, respectively). These data imply that the dolomite cement precipitated from higher temperature hydrothermal salinity fluids. These fluids could be related to widespread igneous activities in the Tarim Basin occurring during Permian time when the host dolostones were deeply buried. Faults likely acted as important conduits that channeled dolomitizing fluids from the underlying strata into the basal carbonates, leading to intense dolomitization. Therefore, dolomitization, in the Keping Uplift area is likely related to evaporated seawater via seepage reflux in addition to burial processes and hydrothermal fluids.  相似文献   

6.
Dolomites from the productive Osa horizon (upper subformation of the Lower Cambrian Bilir Formation) in the Talakan petroleum field show a prominent 1–2‰ decrease in δ18O (from 23–24 to 21–22‰), which presumably marks a zone of relatively high water/rock ratios. Productive boreholes are characterized by moderate δ34S values (from 25.1 to 30.6‰) and negative correlation between δ34S in anhydrite and δ18O in associated dolomite, which points to a partial sulfate reduction during catagenesis. In nonproductive borehole, δ34S values increase significantly (from 31.4 to 35.6‰) and show positive correlation with δ18O in dolomite. Rocks recovered by nonproductive borehole possibly recrystallized during early diagenesis, and, correspondingly lost their permeability and capacity to form pores. Limestones and dolomites of the Osa horizon have a carbon isotopic composition within the range of normal marine carbonates (δ13C = 0 ± 1 ‰), which does not indicate a significant role of organic matter in postsedimentary recrystallization of carbonate sediments. A positive δ13C excursion up to 4.5‰ recorded in the lower subformation of the Bilir Formation presumably occurred at the sedimentation stage under conditions of high rates of bioproductivity and organic matter burial in sediments.  相似文献   

7.
Magnesite forms a series of 1‐ to 15‐m‐thick beds within the ≈2·0 Ga (Palaeoproterozoic) Tulomozerskaya Formation, NW Fennoscandian Shield, Russia. Drillcore material together with natural exposures reveal that the 680‐m‐thick formation is composed of a stromatolite–dolomite–‘red bed’ sequence formed in a complex combination of shallow‐marine and non‐marine, evaporitic environments. Dolomite‐collapse breccia, stromatolitic and micritic dolostones and sparry allochemical dolostones are the principal rocks hosting the magnesite beds. All dolomite lithologies are marked by δ13C values from +7·1‰ to +11·6‰ (V‐PDB) and δ18O ranging from 17·4‰ to 26·3‰ (V‐SMOW). Magnesite occurs in different forms: finely laminated micritic; stromatolitic magnesite; and structureless micritic, crystalline and coarsely crystalline magnesite. All varieties exhibit anomalously high δ13C values ranging from +9·0‰ to +11·6‰ and δ18O values of 20·0–25·7‰. Laminated and structureless micritic magnesite forms as a secondary phase replacing dolomite during early diagenesis, and replaced dolomite before the major phase of burial. Crystalline and coarsely crystalline magnesite replacing micritic magnesite formed late in the diagenetic/metamorphic history. Magnesite apparently precipitated from sea water‐derived brine, diluted by meteoric fluids. Magnesitization was accomplished under evaporitic conditions (sabkha to playa lake environment) proposed to be similar to the Coorong or Lake Walyungup coastal playa magnesite. Magnesite and host dolostones formed in evaporative and partly restricted environments; consequently, extremely high δ13C values reflect a combined contribution from both global and local carbon reservoirs. A 13C‐rich global carbon reservoir (δ13C at around +5‰) is related to the perturbation of the carbon cycle at 2·0 Ga, whereas the local enhancement in 13C (up to +12‰) is associated with evaporative and restricted environments with high bioproductivity.  相似文献   

8.
Using the clumped isotope method, the temperature of dolomite and calcite formation and the oxygen isotopic composition (δ18Ow) of the diagenetic fluids have been determined in a core taken from the Arab‐D of the Ghawar field, the largest oil reservoir in the world. These analyses show that while the dolomites and limestones throughout the major zones of the reservoir recrystallized at temperatures between ca 80°C and 100°C, the carbonates near the top of the reservoir formed at significantly lower temperatures (20 to 30°C). Although the δ18O values of the diagenetic fluids show large variations ranging from ca <0‰ to ca +8‰, the variations exhibit consistent downhole changes, with the highest values being associated with the portion of the reservoir with the highest permeability and porosity. Within the limestones, dolomites and dolomites associated with the zone of high permeability, there are statistically significant different trends between the δ18Ow values and recrystallization temperature. These relationships have different intercepts suggesting that fluids with varying δ18Ow values were involved in the formation of dolomite and limestone compared to the formation of dolomite associated with the zone of high permeability. These new data obtained using the clumped isotope technique show how dolomitization and recrystallization by deep‐seated brines with elevated δ18Ow values influence the δ18O values of carbonates, possibly leading to erroneous interpretations unless temperatures can be adequately constrained.  相似文献   

9.
The Middle Muschelkalk (Middle Triassic) of the Catalan Coastal Range (north-east Spain) comprises sandstone, mudstone, anhydrite and minor carbonate layers. Interbedded sandstones and mudstones which are dominant in the north-eastern parts of the basin are terminal alluvial fan deposits. South-westward in the basin, the rocks become dominated by interbedded evaporites and mudstones deposited in sabkha/mudflat environments. The diagenetic and pore water evolution patterns of the Middle Muschelkalk suggest a strong facies control. During eodiagenesis, formation of microdolomite, anhydrite, baryte, magnesite, K-feldspar and mixed-layer chlorite/smectite was favoured within and adjacent to the sabkha/mudflat facies, whereas calcite, haematite, mixed-layer illite/smectite and quartz formed mainly in the alluvial facies. Low δ18OSMOW values for microdolomite (+23.7 to +28.4%) and K-feldspar overgrowths (+17.3 to +17.7%) suggest either low-temperature, isotopic disequilibrium or precipitation from low-18O porewaters. Low-18O waters might have developed, at least in part, during low-temperature alteration of volcanic rock fragments. During mesodiagenesis, precipitation of quartz overgrowths and coarse dolomite occurred in the alluvial sandstones, whereas recrystallization of microdolomite was dominant in the sabkha/mudflat facies. The isotopic compositions of these mesogenetic phases reflect increasing temperature during burial. Upon uplift and erosion, telogenetic calcite and trace haematite precipitated in fractures and replaced dolomite. The isotopic composition of the calcite (δ18OSMOW=+21.5 to +25.6%o; δ13C= 7.7 to - 5.6%o) and presence of haematite indicate infiltration of meteoric waters.  相似文献   

10.
Peritidal carbonates of the Lower Jurassic (Liassic) Gibraltar Limestone Formation, which form the main mass of the Rock of Gibraltar, are replaced by fine and medium crystalline dolomites. Replacement occurs as massive bedded or laminated dolomites in the lower 100 m of an ≈460‐m‐thick platform succession. The fine crystalline dolomite has δ18Ο values either similar to, or slightly higher than, those expected from Early Jurassic marine dolomite, and δ13C values together with 87Sr/86Sr ratios that overlap with sea‐water values for that time, indicating that the dolomitizing fluid was Early Jurassic sea water. Absence of massive evaporitic minerals and/or evaporite solution‐collapse breccias in these carbonate rocks indicates that the salinity of sea water during dolomitization was below that of gypsum precipitation. The occurrence of peritidal facies, a restricted microbiota and rare gypsum pseudomorphs are also consistent with penesaline conditions (salinity 72–199‰). The medium crystalline dolomite has some δ18Ο and δ13C values and 87Sr/86Sr ratios similar to those of Early Jurassic marine dolomites, which indicates that ambient sea water was again a likely dolomitizing fluid. However, the spread of δ18Ο, δ13C and 87Sr/86Sr values indicates that dolomitization occurred at slightly increased temperatures as a result of shallow (≈500 m) burial or that dolomitization was multistage. These data support the hypothesis that penesaline sea water can produce massive dolomitization in thick peritidal carbonates in the absence of evaporite precipitation. Taking earlier models into consideration, it appears that replacement dolomites can be produced by sea water or modified sea water with a wide range of salinities (normal, penesaline to hypersaline), provided that there is a driving mechanism for fluid migration. The Gibraltar dolomites confirm other reports of significant Early Jurassic dolomitization in the western Tethys carbonate platforms.  相似文献   

11.
Diagenetically altered Pleistocene dolomite occurs in the shallow subsurface of the Arabian Gulf, offshore of Al Jubayl, Saudi Arabia. This dolomite accumulated in relatively shallow marine to sabkha depositional environments. In contrast with the thin extent of most other Quaternary sabkha and sabkha-related dolomite deposits, these deposits comprise a thick (>56 m) accumulation. Additionally, this Pleistocene dolomite displays a high degree of ordering and has a more nearly ideal stoichiometric composition than the dolomite from the depositionally and diagenetically analogous Abu Dhabi sabkha complex. The Pleistocene dolomite also has lower δ13 and δ18O values than the modern Abu Dhabi sabkha dolomite, and higher values than those commonly reported for analogous dolomite from the ancient rock record. The low δ18O values, in conjunction with the geological setting, indicate that the diagenetic waters were meteoric or mixed meteoric and marine in composition. Thus, the degree of ordering, stoichiometric and stable isotopic values indicate that this dolomite has undergone diagenetic alteration relative to its presumed Holocene precursor.  相似文献   

12.
塔里木盆地寒武-奥陶系白云岩储层类型与分布特征   总被引：6，自引：3，他引：3  
塔里木盆地寒武-奥陶系白云岩是台盆区最重要的储层之一,发育4种类型:①潮坪白云岩。以含膏泥晶白云岩为主,石膏溶孔及白云岩砾间孔发育,发育于潮间-潮上坪蒸发环境。白云石表现为MgO-CaO呈线性正相关、低Mg/Ca值及高∑REE值、锶同位素值分布在0.7085～0.7100之间,略高于同期海水值0.7090、阴极发光不发光或暗色光。储层分布主要受沉积相控制,发育于中下寒武统地层;②蒸发台地白云岩。以藻丘及颗粒灰岩选择性白云石化为特征,发育铸模孔、膏溶孔和残留粒间孔,白云石Mg/Ca值变化范围大、δ13C、δ18O值相对偏正、分别大于2‰和-4‰、阴极发光发较亮红光。储层主要发育于台内靠近台缘一侧;③埋藏白云岩。发育细晶、中晶及粗晶白云岩,以晶间孔及晶间溶孔为主,δ18O值偏负在-5‰～-10‰(PDB)之间,87Sr/86Sr值相对较大,为0.7090～0.7110,阴极发光以发暗棕褐色、紫色光为主。埋藏白云岩储层发育主要受成岩相控制,但也表现出与沉积相具有相关性,这是因为物性好的台缘、台内礁滩体及有裂缝沟通构成的开放体系更有利于埋藏白云石化作用发生;④热液白云岩。以受热液改造的结晶白云岩为特征,往往伴生热液矿物,白云石δ18O值异常偏负、一般小于-9‰(PDB)、阴极发光多发明亮红光、稀土元素标准化配分曲线中Eu出现正异常、出现高于地层背景值的异常高温包裹体;主要发育在具有上覆隔挡层的不整合面之下地层及大断裂发育带附近。上述四类白云岩在规模与分布上有不同,但都可预测。埋藏和热液白云岩规模较大,受原始沉积相带和成岩流体来源双重约束。潮坪和蒸发台地白云岩规模可变性较大,可由沉积环境重建,结合成岩相研究预测评价。  相似文献   

13.
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   

14.
C and O isotope composition of Middle-Upper Miocene and Lower Pliocene carbonates from Kerch-Taman Region (Eastern Paratethys) have been studied in order to reconstruct palaeoenvironmental variability and post-sedimentation changes. The δ13C and δ18О values of the Upper Sarmatian to Lower Pliocene organogenic carbonates reflect the desalinization of paleobasins, global Late Miocene Cooling, and increase in seasonal temperature fluctuations. Isotopic composition of the Middle Sarmatian organogenic carbonates was strongly influenced by evaporation processes, high bioproductivity, and local submarine methane emissions. Warm climate and low bioproductivity together with unstable hydrological regime during the Late Chokrakian and the Karaganian times influenced the isotope composition of primary carbonates. Calcite shell of Spiratella sp. (δ13C =–0.4‰ and δ18О =–0.4‰) from Tarkhanian sediments was formed in warm marine environment. Dolomitization prevails over other secondary mineralization in the studied carbonate rocks. Two groups of secondary dolomites that are characterized by negative and positive δ13C values have been recognized. Lowe δ13C values (up to–31.4‰) in dolomites indicate the influence of both dissolved inorganic carbon (DIC) from oxidized organic matter (Сorg) and methane. Dolomites with positive δ13C values (7.0 and 7.8‰) associat with migration of CO2- and CH4-containing saline groundwater.  相似文献   

15.
1980年6月,本文作者之一的K. Kelts曾去美国参加由经济古生物学者和矿物学者协会组织的地质旅行。该行主要是观察和研究怀俄明州西南始新统绿河组的沉积环境。对此次旅行中带回瑞士苏黎世联邦理工学院地质研究所的样品,曾作了切片、X-射线衍射和碳氧同位素分析。  相似文献   

16.
Upper Pliocene dolomites (‘white earth’) from La Roda, Spain, offer a good opportunity to evaluate the process of dolomite formation in lakes. The relatively young nature of the deposits could allow a link between dolomites precipitated in modern lake systems and those present in older lacustrine formations. The La Roda Mg‐carbonates (dolomite unit) occur as a 3·5‐ to 4‐m‐thick package of poorly indurated, white, massive dolomite beds with interbedded thin deposits of porous carbonate displaying root and desiccation traces as well as local lenticular gypsum moulds. The massive dolomite beds consist mainly of loosely packed 1‐ to 2‐μm‐sized aggregates of dolomite crystals exhibiting poorly developed faces, which usually results in a subrounded morphology of the crystals. Minute rhombs of dolomite are sparse within the aggregates. Both knobbly textures and clumps of spherical bodies covering the crystal surfaces indicate that bacteria were involved in the formation of the dolomites. In addition, aggregates of euhedral dolomite crystals are usually present in some more clayey (sepiolite) interbeds. The thin porous carbonate (mostly dolomite) beds exhibit both euhedral and subrounded, bacterially induced dolomite crystals. The carbonate is mainly Ca‐dolomite (51–54 mol% CaCO3), showing a low degree of ordering (degree of ordering ranges from 0·27 to 0·48). Calcite is present as a subordinate mineral in some samples. Sr, Mn and Fe contents show very low correlation coefficients with Mg/Ca ratios, whereas SiO2 and K contents are highly correlated. δ18O‐ and δ13C‐values in dolomites range from ?3·07‰ to 5·40‰ PDB (mean=0·06, σ=1·75) and from ?6·34‰ to ?0·39‰ PDB (mean=?3·55, σ=1·33) respectively. Samples containing significant amounts of both dolomite and calcite do not in general show significant enrichment or depletion in 18O and 13C between the two minerals. The correlation coefficient between δ18O and δ13C for dolomite is extremely low and negative (r=?0·05), whereas it is higher and positive (r=0·47) for calcite. The lacustrine dolomite deposit from La Roda is interpreted mainly as a result of primary precipitation of dolomite in a shallow, hydrologically closed perennial lake. The lake was supplied by highly saturated HCO3?/CO32? groundwater that leached dolomitic Mesozoic formations. Precipitation of dolomite from alkaline lake waters took place under a semi‐arid to arid climate. However, according to our isotopic data, strong evaporative conditions were not required for the formation of the La Roda dolomite. A significant contribution by bacteria to the formation of the dolomites is assumed in view of both petrographic and geochemical evidence.  相似文献   

17.
A. Sáez  L. Cabrera 《Sedimentology》2002,49(5):1073-1094
ABSTRACT A small, closed, lacustrine system developed during the restraining overstep stages of the Oligocene As Pontes strike‐slip basin (Spain). The increase in basin accommodation and the headward spread of the drainage, which increased the water input, triggered a change from shallow, holomictic to deeper, meromictic conditions. The lower, shallow, lacustrine assemblage consists of mudstone–carbonate cycles recording lacustrine–palustrine ramp deposition in a saline lake. High Sr content in some early diagenetic calcites suggests that aragonite and calcite made up the primary carbonate muds. Early dolomitization took place together with widespread pedogenic activity. The upper, deep, freshwater, lacustrine assemblage includes bundles of carbonate–clay rhythmites and fine‐grained turbidite beds. Primary calcite and diagenetic siderite make up the carbonate laminae. The Mg content of the primary carbonates records variations in Mg/Ca ratios in lacustrine waters. δ18O and δ13C covariance trends in calcite reinforce closed drainage conditions. δ18O data indicate that the lake system changed rapidly from short‐lived isotopically light periods (i.e. from seasonal to pluriannual) to longer steady‐state periods of heavier δ18O (i.e. from pluriannual to millennial). The small δ13C changes in the covariant trends were caused by dilute inflow, changing the contributions of dissolved organic carbon in the system and/or internal variations in lacustrine organic productivity and recycling. In both shallow and deep carbonate facies, sulphate reduction and methanogenesis may account, respectively, for the larger negative and positive δ13C shifts recorded in the early diagenetic carbonates (calcite, dolomite and siderite). The lacustrine system was very susceptible to high‐frequency, climatically forced water balance variations. These climatic oscillations interfered with the low‐frequency tectonic and morphological changes in the basin catchment. This resulted in the superposition of high‐order depositional, mineralogical and geochemical cycles and rhythms on the lower order lacustrine infill sequence.  相似文献   

18.
《Sedimentary Geology》2006,183(3-4):181-202
Kita-daito-jima is a carbonate island located at the northwestern region of the Philippine Sea (25°55.6′–57.6′N, 131°16.9′–19.8′E). Dolomites extend from the island surface to a depth of 100 m below the ground surface (mbgs). Strontium isotope stratigraphy indicates that subsurface Units C1 (0–49.7 mbgs) and C2 (49.7–103.4 mbgs) were dolomitized at 5.5 Ma and 2.0 Ma, respectively, and that island-surface dolomites are products of dolomitization at 1.6–2.0 Ma. X-ray diffraction analysis indicates that the island-surface and borehole dolomites comprise variable mixtures of four and three dolomite crystal phases, respectively. Each of these phases is distinguished by a different Ca and Mg content. Three textural types can be recognized in the Kita-daito-jima dolomites, fabric-preserving crystalline nonmimetic (CNM), crystalline mimetic (CM), and fabric-preserving microsucrosic (MS). CNM dolomites contain more calcian phases, whereas MS dolomites commonly are richer in more stoichiometric phases. Backscattered electron images indicate that calcian dolomite phases were precipitated earlier than the more stoichiometric dolomite phases and that there is no significant hiatus between the phases, although they are diachronous. Both the island surface and borehole cores dolomites show linear relationships between whole-rock δ18O composition and Mg contents and between whole-rock trace element concentrations (Sr and Na) and Mg contents. These covariances result from phase mixing, not stoichiometric effects. Deconvolution of whole-rock isotopic and elemental compositions based on the relative abundance of phases reveals that each phase has a distinct chemical and isotopic composition. Oxygen isotopic compositions of the island surface and borehole dolomites suggest that all dolomite phases formed in seawater and that dolomitization primarily occurred during glacio-eustatic sea-level lowstands and cooler ocean temperatures.  相似文献   

19.
Cambrian dolostone reservoirs in the Tarim Basin, China, have significant potential for future discoveries of petroleum, although exploration and production planning is hampered by limited understanding of the occurrence and distribution of dolomite in such ancient rocks buried to nearly 8 km. The study herein accessed new drill core samples which provide an opportunity to understand the dolomitization process in deep basins and its impact on Cambrian carbonate reservoirs. This study documents the origin of the dolostone reservoirs using a combination of petrology, fluid‐inclusion microthermometry, and stable and radiogenic‐isotopes of outcrop and core samples. An initial microbial dolomitization event occurred in restricted lagoon environments and is characterized by depleted δ13C values. Dolomicrite from lagoonal and sabkha facies, some fabric‐retentive dolomite and fabric‐obliterative dolomite in the peloidal shoal and reef facies show the highest δ18O values. These dolomites represent relatively early reflux dolomitization. The local occurrence of K‐feldspar in dolomicrite indicates that some radiogenic strontium was contributed via terrigenous input. Most fabric‐retentive dolomite may have precipitated from seawater at slightly elevated temperatures, suggested by petrological and isotopic data. Most fabric‐obliterative dolomite, and medium to coarse dolomite cement, formed between 90°C and 130°C from marine evaporitic brine. Saddle dolomite formed by hydrothermal dolomitization at temperatures up to 170°C, and involved the mixing of connate brines with Sr‐ enriched hydrothermal fluids. Intercrystalline, moldic, and breccia porosities are due to the early stages of dolomitization. Macroscopic, intergranular, vuggy, fracture and dissolution porosity are due to burial‐related dissolution and regional hydrothermal events. This work has shown that old (for example, Cambrian or even Precambrian) sucrosic dolomite with associated anhydrite, buried to as much as 8000 m, can still have a high potential for hosting substantial hydrocarbon resources and should be globally targeted for future exploration.  相似文献   

20.
The Early to Middle Cambrian Red Heart Dolomite and lower Arthur Creek Formation of the southern portion of the Georgina Basin, Australia, is an entirely dolomitized succession of shallow-water evaporitic mudflat and deeper-water subtidal lithologies. Three types of dolomite have been identified and are interpreted as: (1) syndepositional dolomite; (2) regional replacement dolomite; and (3) void-filling dolomite (cement). Syndepositional dolomite, derived from saline pore fluids developed in a sabkha environment, is a minor dolomite type with very fine crystal mosaics and has a mottled, non-zoned cathodoluminescence. The widespread regional replacement dolomite ranges from fine- to medium-crystalline forming mainly planar-s and non-planar-a crystal mosaics, and displays blotchy, mottled, non-zoned cathodoluminescence. Void-filling dolomite commonly forms planar-s to planar-e, medium to very coarse crystal mosaics. Rare non-planar-c, very coarsely crystalline saddle dolomite also exists. Void-filling dolomite has a successively zoned cathodoluminescence pattern from non-, to brightly, to dully luminescent. Geochemically, the syndepositional dolomite has δ18O (PDB) values ranging between ? 5.3 and ? 8.6%o. Regional replacement dolomites exhibit a wide range of δ18O values from ? 3.3 to ? 10.9%o whereas void-filling dolomite has δ18O values ranging from ? 10.8 to ? 14.3%o. All three dolomite types have similar δ13C (PDB) values, in the range between +1.7 and ?1.7%o. Three initial dolomitization episodes are interpreted: (1) a sabkha stage, forming the syndepositional dolomite and dolomitizing the evaporitic mudflat lithologies; (2) a brine-reflux stage, replacing the subtidal lithologies; and (3) a burial stage, forming the void-filling dolomite type. Final dolomite stabilization occurred during burial, at elevated temperatures, in the presence of basinal fluids, resulting in progressive recrystallization and stabilization of the earlier-formed syndepositional and replacement dolomites. Both textural and geochemical evolution should be taken into account when studying the origin of dolomites, based on their present geochemical composition. Sulphates are represented by very fine-crystalline syndepositional anhydrite in association with the syndepositional dolomite, and coarse to very coarse anhydrite cement. Evaportic mudflat (sabkha) and burial environments are inferred for the origin of the former and the latter anhydrite types, respectively. Evaporite dissolution breccias, indicative of the former presence of evaporites, are common throughout the succession.  相似文献   

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