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1.
陡山沱组顶部潮间带泻湖相泥页岩中发现重晶石, 其宏观、微观特征以及测试分析结果表明为早期成岩成因。结合产出层位沉积和地球化学特征认为, 陡山沱组沉积中期和末期发生显著海平面下降, 导致沉积速率降低至无沉积或沉积间断, 使已埋藏有机质暴露、氧化和陆源物质输入增加, 从而导致早期成岩重晶石和大型钙质结核发育和δ13C高负异常等。深水环境的变迁可能是导致陡山沱组下部发育的大型具刺疑源类生物灭绝的原因。野外沉积学特征考察显示, 陡山沱组底部、内部以及与灯影组接触部位可能存在沉积间断、饥饿沉积或平行不整合。上述研究对深入理解陡山沱组顶部年龄、早期生物演化、辐射以及Ediacaran地质历史演化具有新的启示作用。 相似文献
2.
The Mn contents and sedimentation rates of two cores from different areas of the Peru Basin have been determined. The southern core is associated with Mn nodules of conventional slow accretion rates (~ mm/106 yr) while the northern one accompanies nodules with very high growth rates (~102 mm/106 yr). The depletion of Mn observed within the top 40 cm of the cores is interpreted as resulting from a diagenetic remobilization of Mn+2 due to the oxidative characteristics of the sedimentary column. In both cores, the calculated flux of Mn provided by the sediment is higher than the total Mn recovered in the overlying nodules. This indicates that the Mn content of the Peru Basin nodules can be supplied by diagenetic processes from the sediment, not only for the slowly growing nodules but also for the extremely fast growing concretions found in the north of the basin. 相似文献
3.
Evaporitic sediments of Early Archaean age from the Warrawoona Group, North Pole, Western Australia 总被引：2，自引：0，他引：2
Chemical sediments are common and diverse in the c. 3500 Myr old North Pole chert-barite unit in the Warrawoona Group, Western Australia. Although almost all original minerals were replaced during hydrothermal alteration, metamorphism and deformation, pseudomorphic relics of sedimentary and diagenetic textures and structures show that at least six lithofacies were partly or wholly chemical in origin. These contained five main chemical sedimentary components: primary carbonate mud, diagenetic carbonate crystals, primary sulphate crystals, diagenetic sulphate crystals and diagenetic sulphate nodules. All show a wide range of characteristics consistent only with a marine evaporative origin. Diagenetic carbonate and sulphate crystals, once ferroan dolomite and gypsum, were precipitated within volcanogenic lutites high on littoral mudflats. The other evaporative phases were apparently deposited behind a barrier bar composed of stranded pumice rafts. Primary sulphate crystals, once gypsum and now barite, were precipitated in semi-permanent pools immediately behind the bar. Primary carbonate mud, originally calcitic or aragonitic but now silicified, was deposited in nearby channels and on surrounding mudflats. Within these sediments, diagenetic carbonate crystals (formerly ferroan dolomite) and diagenetic sulphate nodules and crystals (once gypsum) grew during later desiccation. The existence of these evaporites, and more like them in the sediments of other Early Archaean cratons, suggests that shallow marine and terrestrial conditions prevailed over a small but significant portion of the early Earth, contrary to some models of global tectonic evolution. Their overall similarity with more recent evaporitic deposits indicates that there was greater conformity between conditions in modern and primeval sea-shore environments than might be expected, given the great age difference. The attitude implicit in many accounts of Earth's early history, that evaporites were either not deposited or not preserved in Archaean sediments, thus seems to be incorrect. 相似文献
4.
Chalcedonic quartz and occurrence of quartzine (length-slow chalcedony) in pelagic sediments 总被引：2，自引：0，他引：2
J. B. KEENE 《Sedimentology》1983,30(3):449-454
ABSTRACT Chalcedony is the most abundant form of quartz in silicified pelagic sediments from the North Pacific. Varieties of chalcedonic quartz present in chert of deep-sea origin include chalcedony (length-fast and zebraic), quartzine (length-slow), and lutecite.
These occurrences of quartzine in known pelagic sediments emphasize the dangers of using quartzine as an indicator of former evaporitic environments. Quartzine is a diagenetic mineral and does indicate pore fluids rich in sulphate and magnesium. In pelagic sediments, it is always associated with authigenic barite and in many cases with authigenic dolomite. Quartzine should not be used, by itself, as an indicator of any particular environment of deposition. 相似文献
These occurrences of quartzine in known pelagic sediments emphasize the dangers of using quartzine as an indicator of former evaporitic environments. Quartzine is a diagenetic mineral and does indicate pore fluids rich in sulphate and magnesium. In pelagic sediments, it is always associated with authigenic barite and in many cases with authigenic dolomite. Quartzine should not be used, by itself, as an indicator of any particular environment of deposition. 相似文献
5.
Although it is a pelagic sediment, fine-grained calcareous ooze may be mobilized prior to general lithification and redeposited as allochthonous units. Numerous occurrences of allochthonous chalk have been reported in recent years, having been recognized by large-scale bedding features seen in outcrop. Smaller-scale internal features, such as contorted laminae, and larger features, such as smeared burrows and imbricated flint nodules, attest to a significant amount of soft-sediment deformation and synsedimentary slumping in European chalk sections of Late Cretaceous age. Truly autochthonous chalks contain complex, tiered ichnofabrics and in some cases exhibit a diagenetic nodular fabric that is undisturbed by transport. In some situations, such as stagnant water conditions, autochthonous chalks may exhibit primary lamination, although this is very uncommon in European chalk sequences. Different types of redepositional processes produce an array of varied allochthonous fabrics. Glide and slump units, for example, contain internal deformational features produced during sliding. Ooze flow causes plastic deformation of chalk units, internally as well as externally. Resuspension and fluid flow of chalk sediment produces a deposit having a totally new fabric, such as a conglomerate composed of detrital chalk clasts. In this paper, typical macroscopic, sedimentary fabric types are illustrated, and the means of identifying them are discussed in terms of bioturbation features, in situ diagenetic nodules versus detrital clasts, physical deformation structures and development of flints. 相似文献
6.
Geochemistry of ferromanganese nodules from DOMES site a,Northern Equatorial Pacific: Multiple diagenetic metal sources in the deep sea 总被引：1，自引：0，他引：1
The major and minor element composition of ferromanganese nodules from DOMES Site A has been determined by X-ray fluorescence methods. Three phases appear to control the bulk compositions: Mn and Fe oxyhydroxides and aluminosilicates. Relatively wide compositional variations are evident throughout the area. Nodules with high Mn/Fe ratios, high Cu, Mg, Mo, Ni and Zn concentrations and high todorokite/δ-MnO2 ratios have granular surface textures and are confined to an east-west trending depression with thin Quaternary sediment cover. Nodules with low Mn/Fe ratios, high concentrations of As, Ca, Ce, Co, La, P, Sr, Ti, V, Y and Zr and low todorokite/δ-MnO2 ratios have smooth surfaces and are confined to shallower areas with relatively thick Quaternary sediment to the north and south of the depression.All nodules in the area have compositions which are influenced by diagenesis, but those with the most marked diagenetic signature (high Mn/Fe and Cu/Ni ratios, low Ce/La ratios and more todorokite) are found in areas of very slow or non-existent sedimentation; many of these nodules are actually in contact with outcropping Tertiary sediment. This paradox may be resolved by postulating, by analogy with some shallow-water occurrences, that the nodules accrete from bottom waters which have enhanced particulate and dissolved metal contents derived from diagenetic reaction in areas remote from the site of nodule formation. The metals are supplied in a bottom flow (probably Antarctic Bottom Water) which also erodes, or prevents modern sedimentation in, the depression. Nodules on the flanks of the depression are not evidently affected by this flow and derive at least pan of their constituent metals from diagenetic reaction in the underlying Quaternary sediment.Apparently, abyssal diagenetic nodules can have an immediate and a remote diagenetic metal source. Metal fluxes derived from pore water dissolved metal gradients may not be relevant to particular accreting nodules if a significant fraction of their metals is derived from outside the area in which they form. 相似文献
7.
The mineral barite (BaSO4) can precipitate in a variety of oceanic settings: in the water column, on the sea floor and within marine sediments. The geological setting where barite forms ultimately determines the geochemistry of the precipitated mineral and its usefulness for various applications. Specifically, the isotopic and elemental composition of major and trace elements in barite carry information about the solution(s) from which it precipitated. Barite precipitated in the water column (marine or pelagic barite) can be used as a recorder of changes in sea water chemistry through time. Barite formed within sediments or at the sea floor from pore water fluids (diagenetic or cold seeps barite) can aid in understanding fluid flow and sedimentary redox processes, and barite formed in association with hydrothermal activity (hydrothermal barite) provides information about conditions of crust alteration around hydrothermal vents. The accumulation rate of marine barite in oxic‐pelagic sediments can also be used to reconstruct past changes in ocean productivity. Some key areas for future work on the occurrence and origin of barite include: fully characterizing the mechanisms of precipitation of marine barite in the water column; understanding the role and potential significance of bacteria in barite precipitation; quantifying parameters controlling barite preservation in sediments; determining the influence of diagenesis on barite geochemistry; and investigating the utility of additional trace components in barite. 相似文献
8.
G. J. De Lange 《Geochimica et cosmochimica acta》1986,50(12):2543-2561
Measured pore-water concentrations of iron in interbedded pelagic and turbiditic sediments from the Nares Abyssal Plain are in excellent agreement with sediment colour and measured redox potential. The organic carbon content of these sediments appears to define the redox conditions and consequently the porewater and solid-phase concentration of constituents that are involved in early diagenetic reactions. In the turbiditic sediments the concentration of NO3− generally goes to zero within a sediment depth of 1 m, whereas at 8 m in a pelagic core from the same area the concentration of NO3− is still higher than it is in the bottom water. The pore-water concentration of Mn2+ in the turbiditic sediments increases sharply down to a depth of approximately 3 m and from thereon remains nearly constant due to saturation with respect to Mn, Ca-CO3. The pore water of the turbiditic sediments is also saturated with respect to calcite. The few “diagenetic spikes” in the pore-water concentration of NO3− and Mn2+ and the concentration/depth profile of dissolved iron, H4SiO4 and phosphate all clearly demonstrate the inhomogeneous nature of interbedded pelagic and turbiditic sediments. The simultaneous occurrence of peaks of dissolved iron/silica and of sediment intervals with a relatively high organic carbon content is attributed to enhanced early diagenetic reactions associated with the decomposition of organic matter in these specific intervals. Linked with these reactions is the irregular pore-water concentration of phosphate, which is shown to originate partly from the oxidation of organic matter, but mainly from the desorption of phosphate from iron oxide. Potential concentrations of phosphate are calculated from the stoichiometric early diagenetic reactions and compared with measured concentrations. Due to the unique combination of low porosity and relatively high sedimentation rates, the sediments from the Nares Abyssal Plain are an ideal basis for the study of such interbedded sequences of pelagic and turbiditic deposits. 相似文献
9.
重晶石沉积类型丰富,具有多种成因过程。通常,沉积型重晶石可分为生物、热液、成岩和冷泉重晶石四种类型。富钡与富硫酸盐的流体（海水、早成岩孔隙水或热液流体）及其相互作用过程（水柱、热液系统、沉积柱、沉积物-水界面附近）决定了重晶石的沉积环境、宏微观产出方式、同位素组成及相应的地质意义。另外,根据扬子地区下寒武统富重晶石沉积的地质特征,简述了其各种富集机制的适用性及争论。据此建议,结合埃迪卡拉纪-寒武纪转折时期的古海洋背景,对其进行详细的沉积学及地球化学分析,有助于深化成因认识,弥合分歧。 相似文献
10.
Concretions, isotopes, and the diagenetic history of the Oxford Clay (Jurassic) of central England 总被引：1，自引：0，他引：1
J. D. HUDSON 《Sedimentology》1978,25(3):339-370
In interpreting the results of a petrographic and isotopic study of concretions, a range of subjects is discussed including the original texture of the Oxford Clay sediment, Jurassic palaeotemperatures, the diagenetic history of pore-waters and the palaeo-hydrology of central England. The concretions are all composed predominantly of calcite. They include precompactional, pyrite-rich concretions that later suffered an eposide of brecciation, and others that only commenced to form after compaction had crushed ammonite shells included in the bituminous clay sediment. Petrographic, chemical, and especially carbon isotope data demonstrate a dominantly organic source for the carbon in the early formed concretions. Oxygen isotopes indicate formation at the same temperatures (13-16°C) at which benthic molluscs were living. Concretion growth in pelleted, anaerobic mud proceeded concurrently with bacterial sulphate reduction and pyrite precipitation. Cracking of the concretions started at this stage: in a few concretions, the cracks were also partially filled with brown calcite. During post-compactional growth, δ13C increased and pyrite content decreased, showing waning organic influence; δ18O decreased. The brecciated concretions were intruded by clay in which baryte crystals grew; finally, most remaining voids were filled with strongly-ferroan calcite of δ18O about—7 PDB and δ13C about O PDB. This must indicate strong depletion of the pore waters in 18O. Mechanisms that might lead to this are reviewed. It is concluded that the sequence of mineralogical and chemical changes is most readily explained if originally marine porewaters, first modified by bacterial activity, were flushed from the compacting clays by water of ultimately meteoric origin. This had its source in palaeo-aquifers beneath the Oxford Clay. Speculative attempts are made to relate this history to the geology of the region. 相似文献
11.
VICTOR A. MELEZHIK ANTHONY E. FALLICK† RICHARD A. SMITH‡ DANTA M. ROSSE§ 《Sedimentology》2007,54(6):1389-1416
Calcite septarian concretions from the Permian Beaufort Group in the Maniamba Graben (NW Mozambique) allow controls on the composition and nature of diagenetic fluids to be investigated. The concretions formed in lacustrine siltstones, where they occur in spherical (1 to 70 cm in diameter) and columnar (up to 50 cm long) forms within three closely spaced, discrete beds totalling 2·5 m in thickness. Cementation began at an early stage of diagenesis and entrapped non‐compacted burrows and calcified plant roots. The cylindrical concretions overgrew calcified vertical plant roots, which experienced shrinkage cracking after entrapment. Two generations of concretionary body cement and two generations of septarian crack infill are distinguished. The early generation in both cases is a low‐Mn, Mg‐rich calcite, whereas the later generation is a low‐Mg, Mn‐rich calcite. The change in chemistry is broadly consistent with a time (burial)‐related transition from oxic to sub‐oxic/anoxic conditions close to the sediment–water interface. Geochemical features of all types of cement were controlled by the sulphate‐poor environment and by the absence of bacterial sulphate reduction. All types of cement present have δ13C ranging between 0‰ and −15‰(Vienna Peedee Belemnite, V‐PDB), and highly variable and highly depleted δ18O (down to 14‰ Vienna Standard Mean Ocean Water, V‐SMOW). The late generation of cement is most depleted in both 13C and 18O. The geochemical and isotopic patterns are best explained by interaction between surface oxic waters, pore waters and underground, 18O‐depleted, reducing, ice‐meltwaters accumulated in the underlying coal‐bearing sediments during the Permian deglaciation. The invariant δ13C distribution across core‐to‐rim transects for each individual concretion is consistent with rapid lithification and involvement of a limited range of carbon sources derived via oxidation of buried plant material and from dissolved clastic carbonates. Syneresis of the cement during an advanced stage of lithification at early diagenesis is considered to be the cause of development of the septarian cracks. After cracking, the concretions retained a small volume of porosity, allowing infiltration of anoxic, Ba‐bearing fluids, resulting in the formation of barite. The results obtained contribute to a better understanding of diagenetic processes at the shallow burial depths occurring in rift‐bound, lacustrine depositional systems. 相似文献
12.
Carbonate concretions formed in bathyal and deeper settings have been studied less frequently than those formed in shallow‐marine deposits. Similarly, concretions affected by catagenetic conditions have rarely been reported. Calcite concretions in deep‐marine mudstones and greywackes of the Bardo Unit (Sudetes Mountains, Poland) formed during early diagenesis and were buried to significant depths. Petrographic and geochemical (elemental and stable C and O isotopic) analyses document their formation close to the sediment–water interface, prior to mechanical compaction within the sulphate reduction zone and their later burial below the oil window. Although the concretions were fully formed during early diagenesis, the effects of increased temperature and interaction with late‐diagenetic interstitial fluids can be discerned. During maximum burial, the concretions underwent thorough recrystallization that caused alteration of fabric and elemental and O isotope composition. The initial finely crystalline cement was replaced by more coarsely crystalline, sheaf‐like, poikilotopic calcite in the concretions. These large calcite crystals engulf and partially replace unstable detrital constituents. The extremely low δ18O values (down to ?21·2‰ Vienna Pee Dee Belemnite) in the concretions are the result of the increased temperature in combination with alteration of volcanic glass, both causing a significant 18O‐depletion of bicarbonate dissolved in the interstitial fluids. Recrystallization led to uniform O isotope ratios in the concretions, but did not affect the C isotope signature. The δ13C values of the late‐diagenetic cements precipitated in the greywacke and in cracks cutting through concretions imply crystallization in the catagenetic zone and decarboxylation as a source of the bicarbonate. These late‐diagenetic processes took place in a supposedly overpressured setting, as suggested by clastic dykes and hydrofractures that cut through both concretions and host rock. All of these features show how the effects of early and late diagenesis can be distinguished in such rocks. 相似文献
13.
J. D. HUDSON 《Sedimentology》1982,29(5):639-667
Pyrite occurs both in normal clays and shales with a benthic fauna (Oxford Clay, England, and Lias ε, Germany) and in highly bituminous shales (Lias ε, Germany). In normal shales it is present in small quantities as early framboids, but more conspicuously as internal moulds of fossils, especially ammonites. The pyrite in these is petrographically varied; several types of internal sediments and chamber linings are described and illustrated by reflected-light and scanning electron microscopy. Most striking are pyrite stalactites, suspended from the roofs of ammonite chambers, which were later filled by calcite or baryte. Pyrite formed in reducing micro-environments, while the sediment generally was not wholly anoxic. Most pyrite pre-dates compaction of sediment, breakage of fossils and solution of shell aragonite. Variable rates and conditions of reduction of sea water sulphate are reflected in δ34S values ranging from ?55 to +44. Stalactites probably started to form when the ammonite chambers were partially gas-filled. In the bituminous Lias ε shales pyrite occurs abundantly as early framboids and micro-nodules. Larger nodules show a variety of forms, some of which post-date compaction of the sediment. Pyrite is not associated with the abundant flattened ammonites. δ34S values in shales are grouped about a mode near ?20. Pyrite formed over a long time-span, and throughout the sediment, not just in protected cavities. Contrasts in pyrite types can be related to differing depositional environments and organic contents of the shales. Pyrite is an important mineral in diagenetic mineral parageneses which can be deduced by studying fossil void-fillings and concretions, and which help define the diagenetic history of a shale. 相似文献
14.
R. Raiswell S. H. Bottrell S. P. Dean J. D. Marshall† A. Carr‡ & D. Hatfield 《Sedimentology》2002,49(2):237-254
Carbonate concretions in the Lower Carboniferous Caton Shale Formation contain diagenetic pyrite, calcite and barite in the concretion matrix or in different generations of septarian fissures. Pyrite was formed by sulphate reduction throughout the sediment before concretionary growth, then continued to form mainly in the concretion centres. The septarian calcites show a continuous isotopic trend from δ13C=?28·7‰ PDB and δ18O=?1·6‰ PDB through to δ13C=?6·9‰ PDB and δ18O=?14·6‰ PDB. This trend arises from (1) a carbonate source initially from sulphate reduction, to which was added increasing contributions of methanogenic carbonate; and (2) burial/temperature effects or the addition of isotopically light oxygen from meteoric water. The concretionary matrix carbonates must have at least partially predated the earliest septarian cements, and thus used the same carbonate sources. Consequently, their isotopic composition (δ13C=?12·0 to ?10·1‰ PDB and δ18O=?5·7 to ?5·6‰ PDB) can only result from mixing a carbonate cement derived from sulphate reduction with cements containing increasing proportions of carbonate from methanogenesis and, directly or indirectly, also from skeletal carbonate. Concretionary growth was therefore pervasive, with cements being added progressively throughout the concretion body during growth. The concretions contain barite in the concretion matrix and in septarian fissures. Barite in the earlier matrix phase has an isotopic composition (δ34S=+24·8‰ CDT and δ18O=+16·4‰ SMOW), indicating formation from near‐surface, sulphate‐depleted porewaters. Barites in the later septarian phase have unusual isotopic compositions (δ34S=+6 to +11‰ CDT and δ18O=+8 to +11‰ SMOW), which require the late addition of isotopically light sulphate to the porewaters, either from anoxic sulphide oxidation (using ferric iron) or from sulphate dissolved in meteoric water. Carbon isotope and biomarker data indicate that oil trapped within septarian fissures was derived from the maturation of kerogen in the enclosing sediments. 相似文献
15.
Gins A. de Gea Roque Aguado Jos M. Castro Jos M. Molina Luis O'Dogherty Pedro A. Ruiz-Ortiz 《Cretaceous Research》2008,29(5-6):861
The Carbonero Formation represents a scarce, well documented example of Aptian anoxic facies in the Betic Cordillera. Generally, the Aptian record in the pelagic Subbetic basin is both very discontinuous and affected by frequent hiatuses, but in some subsident areas controlled by extensional faults (as in the Carbonero trough) an interesting record is preserved. The Carbonero Formation is characterised by a thick pelagic succession composed of marls with intercalations of calcareous turbidites and a thick interval of anoxic facies. This interval, dated as early Aptian, most likely represents the local expression of Ocean Anoxic Event 1a in the Subbetic basin. A multidisciplinary study including lithostratigraphy, biostratigraphy, and sedimentology has been carried out in the Carbonero Formation, with special attention to the anoxic interval. A collection of facies and sedimentary features has been characterised and interpreted, including barite concretions, calcareous concretions, black shales, siliceous marls and radiolarites, and calcareous turbidites. All these facies seem to have been deposited under oxygen-depleted conditions on a fault-bounded depression with a high subsidence rate. The accumulation and burial of sediments and the preservation of organic matter were controlled by both local and regional factors, such as the physiography of the basin and tectonic setting, as well as by global factors, such as palaeoceanographic and climatic changes. 相似文献
16.
Phosphate stromatolites from condensed cephalopod limestones, Upper Jurassic, Southern Spain 总被引：3，自引：0，他引：3
Upper Jurassic phosphate stromatolites of the Almola Sierra (Southern Spain) encrust macrofossils and hardgrounds, and form oncoids included within pelagic, condensed fossiliferous limestones. Their accretion was determined by bacterially mediated precipitation of phosphate, by the trapping and binding of fine siliciclastics and pelagic biomicrite and by the encrustation of benthonic foraminifera. Phosphorous, trace elements and rare-earth elements were concentrated from degraded organic matter and seawater by stromatolite-building communities, which mediated the formation of phosphate-rich and Fe-Al-Si-rich organic gels under oxic conditions, favouring the precipitation of amorphous mineral precursors (ACP and Fe-Al-Si oxyhydroxides). The observed Ce-enrichment for some stromatolites is explained by oxidative scavenging of Ce4+ from seawater by Fe—Mn oxyhydroxides. The bacterially mediated gels were able to migrate and fill the voids of the stromatolite structure, and later changed to carbonate-fluorapatite, haematite and poorly crystalline Fe-rich clays under postoxic conditions. Phosphatization of trapped carbonate particles also occurred. The phosphate stromatolites formed on a sediment-starved pelagic swell, during periods of no carbonate sedimentation and hardground development. Stromatolite lamination provides evidence for rhythmic alternation between bacterially mediated phosphogenesis, sedimentation and erosion, suggesting episodic changes in the sedimentary environment. Although some of the parameters that controlled phosphate precipitation associated with the stromatolites (local high organic productivity, sediment starvation, moderate depth of deposition and physicochemical conditions) were similar to those found in modern and ancient phosphogenic settings, the palaeogeographical framework and the intensity of sedimentary processes were different to those of the World's major phosphorite deposits. 相似文献
17.
贵州镇宁乐纪泥盆系重晶石矿热水沉积特征 总被引：6，自引：0，他引：6
贵州镇宁乐纪泥盆系重晶石矿床地质储量3 302万t,属大型矿床类型。通过对矿床沉积结构、构造特征研究发现,矿床（体）中分布:纹层状构造、条带状构造、角砾状构造、碎屑状构造、块状构造等,它们与天柱-大河边重晶石矿、广西古潭热水沉积重晶石岩及北秦岭二郎坪群热水沉积重晶石岩类似,海底热水喷流形成的热水喷流通道相、单一热水沉积岩相及热水混合同生沉积相在镇宁重晶石矿层中广泛分布,共同构成了热水浊流沉积相,这与秦岭泥盆系热水沉积岩（矿）类似,矿层沉积结构、构造及岩相特征很好的记录了海底热水喷流、演化的信息,沉积韵律特征说明了热水喷流由弱-强-弱的变化过程。海底热水喷流沉积形成的镇宁重晶石矿中热水沉积结构、构造及热水沉积岩相发育,是研究古热水喷流沉积成岩、成矿、划分热水沉积岩相的理想场所。 相似文献
18.
A relict mound of Holocene barite (BaSO4) tufa underlies the Flybye Springs, a small, barium‐rich, cold sulphur spring system in the Northwest Territories of Canada. The tufa is composed of relatively pure barite with ≤0·34 wt% Ca2+ and ≤0·77 wt% Sr2+. The mound is made up of coated bubble, raft, undulatory sheet, stromatolitic, coated grain and detrital conglomerate barite tufa. Although previously unreported in barite, these lithotypes are akin to facies found in many carbonate spring deposits. Raft and ooid‐coated grain tufa was formed via ‘inorganic’ barite precipitation in spring water ponds and tributaries where rapid oxidation of sulphide to sulphate established barite supersaturation. Undulatory sheet tufa may have formed by the reaction of dissolved barium with sulphate derived from the oxidation of extracellular polysaccharide‐rich colloidal sulphur films floating in oxygenated, barite‐saturated spring water ponds. Coated bubble, oncoid‐coated grain and stromatolitic tufa with filamentous microfossils was formed in close association with sulphur‐tolerant microbes inhabiting dysoxic and oxygenated spring water tributaries and ponds. Adsorption of dissolved barium to microbial extracellular polysaccharide probably facilitated the development of these ‘biogenic’ lithotypes. Detrital conglomerate tufa was formed by barite cementation of microdetrital tufa, allochthonous lithoclasts and organic detritus, including caribou hair. Biogenic textures, organic artefacts and microfossils in the Flybye barite tufa have survived diagenetic aggradational recrystallization and precipitation of secondary cements, indicating the potential for palaeoecological information to be preserved in barite in the geological record. Similarities between the Flybye barite tufa and carbonate spring deposits demonstrate that analogous textures can develop in chemical sedimentary systems with distinct mineralogy, biology and physiochemistry. 相似文献
19.
贵州镇宁泥盆系大型重晶石矿床地球化学特征及其成因研究 总被引：3，自引：1，他引：2
水城-紫云-南丹深断裂是跨越黔桂两省较为闻名的断裂带,沿断裂带两侧分布一系列矿床类型,贵州镇宁泥盆系大型重晶石矿床位于北西侧。对镇宁大型重晶石矿床的沉积学、地球化学及成矿背景的研究发现,矿石中发育纹层状构造、条带状构造、角砾状构造、碎屑状构造和厚层块状构造等热水沉积构造,常量元素特征揭示该矿床可能形成于以SiO2及含矿硫酸盐流体的同生混合沉积作用。重晶石矿(岩)石中Sr、Zn和W明显富集,显示热水沉积特征,且该重晶石矿(岩)石在lg U-lg Th和Cr-Zr相关图解上也均显示热水沉积特征。稀土配分模式富集轻稀土,δEu表现正异常,δCe表现负异常,具热水喷流成矿特征。因此,认为镇宁大型重晶石矿属海底热水喷流沉积形成的产物。 相似文献
20.
Evolution of the Galicia Interior Basin over the last 60 ka: sedimentary processes and palaeoceanographic implications 
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下载免费PDF全文 Anxo Mena Guillermo Francés Marta Pérez‐Arlucea Till J. J. Hanebuth Vera B. Bender Miguel A. Nombela 《第四纪科学杂志》2018,33(5):536-549
The Galicia Interior Basin (GIB; NW Iberian Peninsula) is located near a critical transition between the subtropical (temperate) and subpolar (cold) gyres of the North Atlantic. It therefore witnesses oceanographic changes driven by global climatic events. This study reports on the recent (latest Pleistocene) sedimentary, palaeoceanographic and palaeoclimatic history of the basin. We integrated analysis of deep‐sea sediment cores retrieved from an E–W transect across the GIB. The analysis indicated three types of sedimentary processes recording glacial (Marine Isotope Stage 2–4) and deglacial events: along‐slope bottom currents (forming contourite deposits), pelagic and hemipelagic sedimentation, and gravitational dislocation. Variation in depositional patterns and sedimentation rates indicate distinctive transport (along‐slope and down‐slope) and depositional processes. These in turn reflect climatic and oceanographic drivers. We interpret changes in sea level from core evidence showing changes in sediment supply. The cores exhibited conspicuous sedimentary evidence of Heinrich events (HEs). The stratigraphic intervals associated with HEs showed significant lateral variation. We suggest that the lateral variation may result from the development of an oceanographic boundary between surface water masses with different temperature and salinity parameters or changes in surface currents which may have introduced relatively warmer water into the GIB during the last glacial period. 相似文献