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1.
Stable isotope data of the foraminiferal carbonate shells and bulk sediment samples from the Central Paratethys were investigated to contribute to better knowledge of the paleoenvironmental changes in Badenian (Middle Miocene). Five benthic (Uvigerina semiornata, U. aculeata, Ammonia beccarii, Elphidium sp. and Heterolepa dutemplei) and three planktonic taxa (Globigerina bulloides, G. diplostoma and Globigerinoides trilobus), characterising the bottom, intermediate and superficial layers of the water column, were selected from the Vienna Basin (W Slovakia). The foraminiferal fauna and its isotope signal point out to temperature-stratified, nutrient-rich and consequently less-oxygenated marine water during the Middle/Late Badenian. Negative carbon isotope ratios indicate increased input of 12C-enriched organic matter to the bottom of the Vienna Basin. Positive benthic δ18O implies that the global cooling tendency recorded in the Middle Miocene has also affected the intramountain Vienna Basin. In this time, the Central Paratethys has been in the process of isolation. Our stable isotope trend suggests that the communication with Mediterranean Sea has been still more or less active on the south of Vienna Basin (Slovak part) in the Late Badenian, whereas the seawater exchange towards north was apparently reduced already during the Middle Badenian.  相似文献   

2.
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   

3.
Secular variations in stable carbon‐isotope values of marine carbonates are used widely to correlate successions that lack high‐resolution index fossils. Various environmental processes, however, commonly may affect and alter the primary marine carbon‐isotope signal in shallow epicratonic basins. This study focuses on the marine carbon‐isotope record from the carbonate–evaporite succession of the upper Katian (Upper Ordovician) Red River Formation of the shallow epicratonic Williston Basin, USA. It documents the carbon‐isotope signal between the two major Ordovician positive shifts in δ13C, the early Katian Guttenberg and the Hirnantian excursions. Eight δ13C stages are identified based on positive excursions, shifts from positive to negative values and relatively uniform δ13Ccarb values. A correlation between carbon‐isotope trends and the relative sea‐level changes based on gross facies stacking patterns shows no clear relation. Based on the available biostratigraphy and δ13C trends, the studied Williston Basin curves are tied to the isotope curves from the North American Midcontinent, Québec (Anticosti Island) and Estonia, which confirm the Late Katian age (Aphelognathus divergens Conodont Zone) of the upper Red River Formation. The differences in the δ13C overall trend and absolute values, coupled with the petrographic and cathodoluminescence evidence, suggest that the carbon‐isotope record has been affected by the syndepositional environmental processes in the shallow and periodically isolated Williston Basin, and stabilized by later burial diagenesis under reducing conditions and the presence of isotopically more negative fluids.  相似文献   

4.
Molybdenum isotopes are increasingly widely applied in Earth Sciences. They are primarily used to investigate the oxygenation of Earth's ocean and atmosphere. However, more and more fields of application are being developed, such as magmatic and hydrothermal processes, planetary sciences or the tracking of environmental pollution. Here, we present a proposal for a unifying presentation of Mo isotope ratios in the studies of mass‐dependent isotope fractionation. We suggest that the δ98/95Mo of the NIST SRM 3134 be defined as +0.25‰. The rationale is that the vast majority of published data are presented relative to reference materials that are similar, but not identical, and that are all slightly lighter than NIST SRM 3134. Our proposed data presentation allows a direct first‐order comparison of almost all old data with future work while referring to an international measurement standard. In particular, canonical δ98/95Mo values such as +2.3‰ for seawater and ?0.7‰ for marine Fe–Mn precipitates can be kept for discussion. As recent publications show that the ocean molybdenum isotope signature is homogeneous, the IAPSO ocean water standard or any other open ocean water sample is suggested as a secondary measurement standard, with a defined δ98/95Mo value of +2.34 ± 0.10‰ (2s).  相似文献   

5.
The Ca isotope variation of 11 Miocene and Pleistocene, authigenic, marine phosphates is rather small compared to the corresponding variation in δ18O values. The δ44Ca values are not correlated with the δ18O values and, therefore, they are not temperature controlled. It is likely that the δ44Ca values of the phosphorites reflect the variation in the δ44Ca values of paleo-seawater but, in contrast to Sr, not the isotopic composition of seawater itself. Furthermore, Ca and Sr isotopic compositions are decoupled with decreasing stratigraphic age of the phosphate peloids with Sr isotopic compositions changing to more radiogenic values while Ca isotopic compositions remain rather stable. All samples have δ44Ca values below present-day seawater values, suggesting that phosphate formation discriminates against heavy Ca isotopes.Phosphorites and carbonaceous sediments have a similar Ca isotopic variation during the Miocene. A systematic and more or less constant shift between marine carbonates and phosphates is observed: the phosphate samples are slightly less enriched in 40Ca compared to carbonates. This shift has been related to a mineral-dependent kinetic mass fractionation during precipitation from seawater. The rather stable δ44Ca value for the 19 to 9 Ma old phosphorites points to a constant δ44Ca fractionation of about 1.1 between seawater and phosphorites during the past and suggests steady-state conditions for the Mid-Miocene seawater (sedimentation flux equals erosion flux).  相似文献   

6.
Meteoric sphaerosiderite lines (MSLs), defined by invariant δ18O and variable δ13C values, are obtained from ancient wetland palaeosol sphaerosiderites (millimetre‐scale FeCO3 nodules), and are a stable isotope proxy record of terrestrial meteoric isotopic compositions. The palaeoclimatic utility of sphaerosiderite has been well tested; however, diagenetically altered horizons that do not yield simple MSLs have been encountered. Well‐preserved sphaerosiderites typically exhibit smooth exteriors, spherulitic crystalline microstructures and relatively pure (> 95 mol% FeCO3) compositions. Diagenetically altered sphaerosiderites typically exhibit corroded margins, replacement textures and increased crystal lattice substitution of Ca2+, Mg2+ and Mn2+ for Fe2+. Examples of diagenetically altered Cretaceous sphaerosiderite‐bearing palaeosols from the Dakota Formation (Kansas), the Swan River Formation (Saskatchewan) and the Success S2 Formation (Saskatchewan) were examined in this study to determine the extent to which original, early diagenetic δ18O and δ13C values are preserved. All three units contain poikilotopic calcite cements with significantly different δ18O and δ13C values from the co‐occurring sphaerosiderites. The complete isolation of all carbonate phases is necessary to ensure that inadvertent physical mixing does not affect the isotopic analyses. The Dakota and Swan River samples ultimately yield distinct MSLs for the sphaerosiderites, and MCLs (meteoric calcite lines) for the calcite cements. The Success S2 sample yields a covariant δ18O vs. δ13C trend resulting from precipitation in pore fluids that were mixtures between meteoric and modified marine phreatic waters. The calcite cements in the Success S2 Formation yield meteoric δ18O and δ13C values. A stable isotope mass balance model was used to produce hyperbolic fluid mixing trends between meteoric and modified marine end‐member compositions. Modelled hyperbolic fluid mixing curves for the Success S2 Formation suggest precipitation from fluids that were < 25% sea water.  相似文献   

7.
Holocene sediments from the Gotland Deep basin in the Baltic Sea were investigated for their Fe isotopic composition in order to assess the impact of changes in redox conditions and a transition from freshwater to brackish water on the isotope signature of iron. The sediments display variations in δ56Fe (differences in the 56Fe/54Fe ratio relative to the IRMM-14 standard) from −0.27 ± 0.09‰ to +0.21 ± 0.08‰. Samples deposited in a mainly limnic environment with oxygenated bottom water have a mean δ56Fe of +0.08 ± 0.13‰, which is identical to the mean Fe isotopic composition of igneous rocks and oxic marine sediments. In contrast, sediments that formed in brackish water under periodically euxinic conditions display significantly lighter Fe isotope signatures with a mean δ56Fe of −0.14 ± 0.19‰. Negative correlations of the δ56Fe values with the Fe/Al ratio and S content of the samples suggest that the isotopically light Fe in the periodically euxinic samples is associated with reactive Fe enrichments and sulfides. This is supported by analyses of pyrite separates from this unit that have a mean Fe isotopic composition of −1.06 ± 0.20‰ for δ56Fe. The supply of additional Fe with a light Fe isotopic signature can be explained with the shelf to basin Fe shuttle model. According to the Fe shuttle model, oxides and benthic ferrous Fe that is derived from dissimilatory iron reduction from shelves is transported and accumulated in euxinic basins. The data furthermore suggest that the euxinic water has a negative dissolved δ56Fe value of about −1.4‰ to −0.9‰. If negative Fe isotopic signatures are characteristic for euxinic sediment formation, widespread euxinia in the past might have shifted the Fe isotopic composition of dissolved Fe in the ocean towards more positive δ56Fe values.  相似文献   

8.
This paper carried out mineral and geochemical studies on a profile through a diagenetic methane-derived authigenic carbonate sample that was collected from southwestern Dongsha area of the northern South China Sea. Five samples locating in the cross-sectional middle mainly consist of dolomite and quartz, and two samples close to the surface have a small amount of Mg-calcite. The δ13C values of the samples vary between ?30.59 and ?0.30 % VPDB, with δ18O values ranging from 3.07 to 3.59 % VPDB, δ44/40Ca values ranging from 1.35 to 1.47 % SRM915a, indicating a contribution of methane to the carbon pool where the precipitation of authigenic carbonates occurred. Based on the isotope values alone, it can not be distinguished if the carbon source is thermogenic gas or a mixture of biogenic methane and marine dissolved inorganic carbon. The δ18O values are in general consistent with dolomite precipitation from a fluid similar to present seawater. The observed small variation might be related to the oxygen isotope composition of seep fluid. The relative small range in calcium isotope values suggests that relatively constant growth conditions and precipitation from seawater. The central part of the carbonate nodule formed under the strong influence of methane seepage, and the external part is less influenced by methane, either due to reduced methane flux to the surface or caused by erosional exhumation of the carbonate nodule from greater depth to the sediment surface.  相似文献   

9.
The oxygen and hydrogen isotopic composition of Eocene and Miocene freshwater cherts in the western United States records regional climatic variation in the Cenozoic. Here, we present isotopic measurements of 47 freshwater cherts of Eocene and Miocene age from the Great Basin of the western United States at two different sites and interpret them in light of regional climatic and tectonic history. The large range of δ18O of terrestrial cherts measured in this study, from 11.2‰ to 31.2‰ (SMOW: Standard Mean Ocean), is shown to be primarily the result of variations in δ18O of surface water. The following trends and patterns are recognized within this range of δ18O values. First, in Cenozoic rocks of northern Nevada, chert δ18O records the same shift observed in authigenic calcite between the Eocene and Miocene that has been attributed to regional surface uplift. The consistent covariation of proxies suggests that chert reliably records and retains a signal of ancient meteoric water isotopic composition, even though our analyses show that chert formed from warmer waters (40°C) than coexisting calcite (20°C). Second, there is a strong positive correlation between δ18O and δD in Eocene age chert from Elko, Nevada and Salina, Utah that suggests large changes in lake water isotopic composition due to evaporation. Evaporative effects on lake water isotopic composition, rather than surface temperature, exert the primary control on the isotopic composition of chert, accounting for 10‰ of the 16‰ range in δ18O measured in Eocene cherts. From authigenic mineral data, we calculate a range in isotopic composition of Eocene precipitation in the north-central Great Basin of −10 to −14‰ for δ18O and −70 to −100‰ for δD, which is in agreement with previous estimates for Eocene basins of the western United States. Due to its resistance to alteration and record of variations in both δ18O and δD of water, chert has the potential to corroborate and constrain the cause of variations in isotope stratigraphies.  相似文献   

10.
《Applied Geochemistry》1999,14(7):939-951
Strontium isotope ratios are used to identify end-member ground-water compositions at Äspö in southeastern Sweden where the Hard Rock Laboratory (HRL) has been constructed to evaluate the suitability of crystalline rock for the geologic disposal of nuclear waste. The Hard Rock Laboratory is a decline (tunnel) constructed in 1.8 Ga-old granitic rock that forms islands in an archipelago along the Swedish coast. Ground-water samples were obtained for isotopic analyses from boreholes drilled from the surface and from side boreholes drilled within the HRL. Infiltration at Äspö occurs primarily through fractures zones in the granitic bedrock beneath thin soils throughout the area. Because of extremely low Sr concentrations, rain and snow are not important contributors to the Sr isotope budget of the ground-water system. At shallow levels, water percolating downward along fractures and fracture zones acquires a δ87Sr between +9.5 and +10.0‰ and maintains this value downward while Sr concentrations increase by two orders of magnitude. Ground-water samples from both boreholes and from in the HRL show the effects of mixing with saline waters containing as much as 59 mg/L Sr and δ87Sr values as large as +13.9‰. Baltic Sea water is a potential component of the groundwater system with δ87Sr values only slightly larger than modern marine values (+0.3‰) but with much lower concentrations (1.5 mg/L) than ocean water (8 mg/L). However, because of large Sr concentration differences between the saline groundwater (59 mg/L) and Baltic Sea water (1.5 mg/L), δ87Sr values are not particularly sensitive indicators of sea-water intrusion even though their δ87Sr values differ substantially.  相似文献   

11.
Iron isotope compositions in marine pore fluids and sedimentary solid phases were measured at two sites along the California continental margin, where isotope compositions range from δ56Fe = −3.0‰ to +0.4‰. At one site near Monterey Canyon off central California, organic matter oxidation likely proceeds through a number of diagenetic pathways that include significant dissimilatory iron reduction (DIR) and bacterial sulfate reduction, whereas at our other site in the Santa Barbara basin DIR appears to be comparatively small, and production of sulfides (FeS and pyrite) was extensive. The largest range in Fe isotope compositions is observed for Fe(II)aq in porewaters, which generally have the lowest δ56Fe values (minimum: −3.0‰) near the sediment surface, and increase with burial depth. δ56Fe values for FeS inferred from HCl extractions vary between ∼−0.4‰ and +0.4‰, but pyrite is similar at both stations, where an average δ56Fe value of −0.8 ± 0.2‰ was measured. We interpret variations in dissolved Fe isotope compositions to be best explained by open-system behavior that involves extensive recycling of Feflux. This study is the first to examine Fe isotope variations in modern marine sediments, and the results show that Fe isotopes in the various reactive Fe pools undergo isotopic fractionation during early diagenesis. Importantly, processes dominated by sulfide formation produce high-δ56Fe values for porewaters, whereas the opposite occurs when Fe(III)-oxides are present and DIR is a major pathway of organic carbon respiration. Because shelf pore fluids may carry a negative δ56Fe signature it is possible that the Fe isotope composition of ocean water reflects a significant contribution of shelf-derived iron to the open ocean. Such a signature would be an important means for tracing iron sources to the ocean and water mass circulation.  相似文献   

12.
The Ohori ore deposit is one of the Cu–Pb–Zn deposits in the Green Tuff region, NE Japan, and consists of skarn‐type (Kaninomata) and vein‐type (Nakanomata) orebodies. The former has a unique origin because its original calcareous rocks were made by hydrothermal precipitation during Miocene submarine volcanism. Carbon and oxygen isotope ratios of skarn calcite and sulfur isotope ratios of sulfides were measured in and around the deposit. Carbon and oxygen isotope ratios of the skarn calcite are δ13C = ?15.51 to ?5.1‰, δ18O = +3.6 to +22.5‰. δ13C values are slightly lower than those of the Cretaceous skarn deposits in Japan. These isotope ratios of the Kaninomata skarn show that the original calcareous rocks resemble the present submarine hydrothermal carbonates at the CLAM Site, Okinawa Trough, than Cenozoic limestones, even though some isotopic shifts had occurred during later skarnization. δ34S ratios of the sulfide minerals from the Kaninomata and Nakanomata orebodies are mostly in a narrow range of +4.0 to +7.0‰ and they resemble each other, suggesting the same sulfur origin for the both deposits. The magnetite‐series Tertiary Kaninomatasawa granite is distributed just beneath the skarn layer and has δ34S ratios of +7.5 to 8.1‰. The heavy sulfur isotope ratio of the skarn sulfides may have been affected by the Kaninomatasawa granite.  相似文献   

13.
The stable isotope geochemistry of Miocene sediments from the leeward margin of the Great Bahama Bank was examined to investigate burial diagenetic processes in periplatform carbonates. Data indicate that, in addition to differences in bulk proportions of neritic and pelagic carbonate along the slope, rhythmic variation in primary carbonate content has controlled patterns of burial diagenesis and associated geochemical signatures throughout much of the succession examined. The present study focuses on Ocean Drilling Program Sites 1006 and 1007, the most distal of five sites drilled from marginal to deep basin environments during Leg 166. These Miocene sections are characterized by their cyclic appearance, manifest as decimetre‐ to metre‐scale alternations between light‐coloured ooze/chalk/limestone and dark‐coloured marl/marlstone. The section at Site 1006 contains a high proportion of pelagic carbonate and is unlithified to a subbottom depth of ～675 m. Fluctuations in δ18O and δ13C values at this site are independent of lithological variation and reflect primary conditions. At Site 1007, located at the toe‐of‐slope and composed of a mixture of bank‐derived and pelagic carbonate, limestones are densely cemented, show little evidence of compaction and have δ18O values up to 2‰ higher than coeval sediments at Site 1006. Marlstones at Site 1007 are poorly cemented, exhibit an increase in compaction‐related features with depth and have lower and more variable δ18O values that are similar to those of coeval sediments at Site 1006. Isotopic and petrographic characteristics of limestone interbeds result from cement precipitation from cold sea water during the first ～100 m of burial. Higher proportions of insoluble materials and pelagic carbonate seem to have inhibited diagenetic alteration in adjacent marlstones; in spite of significant compaction and pressure solution during burial, original isotopic compositions appear to be best preserved in these intervals at Site 1007. The documented contrasts in petrographic and isotopic patterns illustrate the role of primary sediment composition in controlling lithification processes in periplatform carbonates and stress the importance of considering such factors when interpreting geochemical data from ancient shelf and slope limestones.  相似文献   

14.
The Miocene palaeogeographic evolution of the Paratethys Sea is still poorly constrained. Here, we use modern Mediterranean biochronology to provide an up‐to‐date overview of changing seas in Central Europe. Instead of a Paratethys that waxed and waned with fluctuating global sea levels, we show that the development of different seas was mainly controlled by tectonic phases. The Early Miocene “Ottnangian Sea” (~18 Ma) was connected to the Mediterranean via the Rhône valley, while the “Karpatian Sea” (~16.5 Ma) was initiated by a tectonically induced marine transgression through the Trans‐Tethyan gateway. In most Central European basins, the establishment of the “Badenian Sea” (<15.2 Ma), triggered by subduction‐related processes in the Pannonian and Carpathian domain, is significantly younger (by ~1 Myr) than usually estimated. The updated palaeogeographic reconstructions provide a better understanding of the concepts of basin dynamics, land–sea distribution and palaeoenvironmental change in the Miocene of Central Europe.  相似文献   

15.
The reconstruction of regional long-term patterns recorded in marine sedimentary successions of the Eastern Paratethys is important in understanding the role of Cenozoic climate change and orogenic activity on the depositional environment and sedimentation dynamics in Western Asia. In this study, the environmental conditions in the early to middle Miocene (Islam Dağ section) in eastern Azerbaijan are elucidated using petrographic–mineralogical relations, detrital indicators, weathering indices and δ13C and δ18O signatures of organic-rich (total organic carbon: ca 3 to 6 wt. %) argillites. Sedimentary facies and chemical proxies (Na/K, K/Al, Si/Al, Ti/Al ratios, chemical index of alteration values) indicate arid conditions, reduced weathering rates in the hinterland and sediment deposition in an euhaline and poorly oxygenated deep-water basin during the early Miocene, followed by a shift to humid conditions, higher weathering rates and an oxygenated water column in the mid-early Miocene. Long-term aridification and deposition of gypsiferous and calcareous argillites under generally more oxygenated, euhaline to polyhaline conditions in a lacustrine or restricted shelf setting until the middle Miocene is evidenced by gradual changes in element ratios and the chemical index of alteration. Discriminant function analysis suggests the Russian Platform, drained by the Palaeo-Volga and Palaeo-Don river systems, to be the source area for the siliciclastic input throughout the Miocene, although a minor contribution of volcanogenic detritus and mafic components from the Greater Caucasus is possible. The C–S–Fe associations and increasing Fe/Al ratios towards the middle Miocene support the concept of continuous influx of detrital Fe and total organic carbon. The formation of ferruginous smectite from alteration of volcanic ash layers could have affected the preservation of total organic carbon and therefore the sedimentary C and Fe budget in the Eastern Paratethys basins. Palaeo-climatic reconstructions based on δ13C (−34·5 to +1·7‰ Vienna Pee Dee Belemnite) and δ18O (−34·7 to −4·8‰ Vienna Pee Dee Belemnite) records of authigenic carbonates should be made with great caution, as the pristine marine signatures may be affected by the oxidation of organic matter and meteoric diagenesis.  相似文献   

16.
High‐resolution marine palynological data have been obtained from two very long sediment cores (MD952009 and MD952010) retrieved from the southern Norwegian Sea. The dinoflagellate cyst assemblages show pronounced fluctuations in composition, which correlate strongly with magnetic susceptibility records and also mimic the δ18O signal of the GISP2 Greenland ice‐core. If focusing on the period from 48 to 30 cal. kyr BP, this correlation suggests a paradoxical response of the sea‐surface environments to the atmospheric conditions over Greenland: when the Greenland δ18O signal reflects warm interstadial conditions, the Norwegian Sea depicts cold sea‐surface temperatures with quasi‐perennial sea‐ice cover (based on dinoflagellate cysts). In contrast, when the Greenland δ18O records cold stadial periods, the Norwegian Sea‐surface temperatures are warm (based on dinoflagellate cysts), probably linked to inflow of the North Atlantic Drift. These results, similar in both cores, are contrary to those of previous studies and shed light on a possible decoupling of Norwegian sea surface‐water conditions and atmospheric conditions over Greenland. This decoupling could be linked to an atmosphere–ocean system behaving similar to that which the Northern Hemisphere is experiencing at present, i.e. strongly variable owing to the North Atlantic Oscillation. Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

17.
High-resolution 230Th/234U ages and δ18O and δ13C compositions of speleothems in Ma’ale Efrayim Cave located to the east of the central mountain ridge of Israel enable us to examine the nature of the rain shadow aridity during glacial and interglacial intervals. Speleothem growth occurred during marine glacial isotopic periods, with no growth during the two last marine isotope interglacial intervals and during the peak of the Last Glacial Maximum. This contrasts with speleothem growth in caves located on the western flank of the central mountain ridge, in the Eastern Mediterranean semiarid climatic zone, which continued throughout the last 240,000 yr. Thus, during glacial periods water reached both sides of the central mountain ridge. A comparison of the present-day rain and cave water isotopic compositions and amounts at the Ma’ale Efrayim Cave site with those on the western flank shows that evaporation and higher temperatures on the eastern flank are major influences on isotopic composition and the lack of rainfall. The δ18O and δ13C profiles of the speleothems deposited between 67,000 and 25,000 yr B.P. match the general trends of the isotopic profiles of Soreq Cave speleothems, suggesting a similar source (eastern Mediterranean Sea) and similar climatic conditions. Thus, during glacial periods the desert boundary effectively migrated further south or east from its present-day location on the eastern flank, whereas interglacial periods appear to have been similar to the present, with the desert boundary at the same position. The decrease in overall temperature and a consequent reduction in the evaporation to precipitation ratios on the eastern flank are viewed as the major factors controlling the decay of the rain shadow effect during glacial periods.  相似文献   

18.
Unusual textural and chemical characteristics of disseminated dolomite in Upper Jurassic shelf sediments of the North Sea have provided the basis for a proposed new interpretation of early diagenetic dolomite authigenesis in highly bioturbated marine sandstones. The dolomite is present throughout the Franklin Sandstone Formation of the Franklin and Elgin Fields as discrete, non‐ferroan, generally unzoned, subhedral to highly anhedral ‘jigsaw piece’ crystals. These are of a similar size to the detrital silicate grains and typically account for ≈5% of the rock volume. The dolomite crystals are never seen to form polycrystalline aggregates or concretions, or ever to envelop the adjacent silicate grains. They are uniformly dispersed throughout the sandstones, irrespective of detrital grain size or clay content. Dolomite authigenesis predated all the other significant diagenetic events visible in thin section. The dolomite is overgrown by late diagenetic ankerite, and bulk samples display stable isotope compositions that lie on a mixing trend between these components. Extrapolation of this trend suggests that the dolomite has near‐marine δ18O values and low, positive δ13C values. The unusual textural and chemical characteristics of this dolomite can all be reconciled if it formed in the near‐surface zone of active bioturbation. Sea water provided a plentiful reservoir of Mg and a pore fluid of regionally consistent δ18O. Labile bioclastic debris (e.g. aragonite, Mg‐calcite) supplied isotopically positive carbon to the pore fluids during shallow‐burial dissolution. Such dissolution took place in response to the ambient ‘calcite sea’ conditions, but may have been catalysed by organic matter oxidation reactions. Bioturbation not only ensured that the dissolving carbonate was dispersed throughout the sandstones, but also prohibited coalescence of the dolomite crystals and consequent cementation of the grain framework. Continued exchange of Mg2+ and Ca2+ with the sea‐water reservoir maintained a sufficient Mg/Ca ratio for dolomite (rather than calcite) to form. Irregular crystal shapes resulted from dissolution, of both the dolomite and the enclosed fine calcitic shell debris, before ankerite precipitation during deep‐burial diagenesis.  相似文献   

19.
It is often argued that the δ18O value of oceanic water was maintained close to 0‰ for hundreds of millions of years, as a consequence of oxygen isotope exchange between oceanic crust and seawater. However, for several decades, the interpretation of the biosedimentary oxygen isotope record has conflicted with the igneous record because, with increasing age, a general trend of decreasing δ18O values (about 6‰) is observed in most carbonates, cherts and phosphates, especially for the Paleozoic and early Mesozoic. We developed a dynamical model of seawater-crust interaction that computes the δ18O value in these two reservoirs as function of time. This model takes into account the continuous production of crust at oceanic ridges, its expansion rate, the permeability profile with space and time, the mineralogical mode of the crust, and the kinetics of oxygen isotope exchange between rock-forming minerals and seawater. The model indicates that the δ18O value of seawater may vary by ±2‰ with a time response ranging from 5 to 50 Ma for expansion rates of 1 to 10 cm.a−1. The variation of ±2‰ is fixed by both integrated water-rock ratio and closure time of the seawater-crust system by sediments. Variations in the oxygen isotope ratio of seawater through time have important implications for the interpretation of the systematically low δ18O values of pre-Jurassic marine sediments. According to our model, marine paleotemperatures could be up to 10°C lower than those expected when applying the classical hypothesis of an ice-free ocean with a δ18O value of −1‰.  相似文献   

20.
The marine benthic fauna and the δ18Oc of foraminifers and ostracods from six sites situated on a west–east transect through central Sweden have been analysed in order to estimate the palaeosalinity and palaeocirculation in this shallow‐marine environment. The measurements have been undertaken on material from the early Preboreal, when the Baltic Basin was in contact with the North Sea through straits in central Sweden. The δ18Oc values have a more negative value towards the east, indicating decreasing salinity. This was the result of limited possibilities for marine water to penetrate into the Baltic Basin and the mixing with freshwater from the melting Fennoscandian ice‐sheet. Four water masses existed in the area: a surface layer of freshwater, marine water from the North Sea, brackish–marine intermediate water on the Swedish west coast and brackish Yoldia Sea water in the Baltic Basin. The chronology is based on radiocarbon dates of marine fossils and, at one site, on the occurrence of the Vedde Ash (10 400–10 300 14C yr BP). This is the first record from marine settings in Sweden. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   

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