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1.
Isotope signatures associated with early meteoric diagenesis   总被引：12，自引：0，他引：12  
The environments in which carbonate diagenesis proceeds have been documented in previous studies of Holocene and late Pleistocene sediments and limestones on Barbados, West Indies. Variations in the carbon and oxygen isotopic composition of limestones, produced during early freshwater diagenesis, have been observed in this study to occur in specific patterns. Six potentially useful patterns emerge when one views stable isotope data within a stratigraphic framework: (1) the subaerial exposure surface is characterized by strongly 12C-enriched limestones. δ13C compositions of underlying limestones grow progressively heavier with increasing depth; (2) the subaerial exposure surface may also be marked by slight 18O-enrichment; (3) an abrupt shift in δ18O values may differentiate sediments above the exposure surface from those below; (4) sediments altered in the marine-meteoric mixing zone may be characterized by positive covariance between their δ18O and δ13C compositions; (5) the vadose-phreatic boundary may be marked by a sharp increase in δ13C values in the seaward portions of a fresh groundwater system; and (6) samples contemporaneously altered in a single fresh groundwater system within an areally restricted region should display a narrow range of δ18O and a wide range of δ13C compositions. Analysis of samples from five Palaeozoic and Mesozoic formations, which contained petrographic evidence of early freshwater diagenesis, showed that isotope patterns similar to those observed in Barbados limestones have been preserved in rocks as old as Mississippian. These isotope patterns could prove to be useful for identifying diagenetically induced porosity trends in carbonate rocks. They might be used to identify limestones diagenetically altered in meteoric environments, to identify mixing zone cements and dolomites, and to trace the regional and vertical distributions of early meteoric groundwater systems in ancient carbonate formations.  相似文献   

2.
Peritidal carbonate rocks (Purbeck facies) of the uppermost Portlandian to Berriasian in the type section of the Sierra del Pozo Formation in the Prebetic Zone, southern Spain, are divisible into 141 shallowing upward cycles averaging 2 m in thickness. The subtidal facies in these cycles consist of micritic or marly limestones with dasycladacean algae and lituolids; the intertidal facies are micritic limestones containing birdseyes and miliolids; the supratidal facies comprise laminated algal limestones, the tops of which display desiccation cracks and rhizocretions, or more locally palaeosols, calcretes, or palaeokarst surfaces. A statistical study, using power spectra of the Fast Fourier Transform, demonstrates that the periodicity of these cycles is in the Milankovitch frequency band. Most sedimentary cycles correspond to the obliquity cycles; eccentricity and precession cycles have also been recognized. Using a Fischer plot, third-order tectono-eustatic cycles are recognized, which can be correlated with the eustatic curve of the Exxon chart. The shallowing upward sequences are characterized by a distinctive pattern of geochemical parameters. Carbon and oxygen isotopic (δ13C and δ18O) variations, calcium and magnesium carbonate contents and the abundance of organic matter and trace elements (Mn and Sr) all have predictable patterns of distribution within the sequences. The Sr content of the subtidal facies is relatively high whereas the δ13C and δ18O ratios are quite low; in the intertidal facies the Sr and Mn levels fall concomitantly with a rise in δ13C and δ18O. The highest δ13C and δ18O values occur in the lower part of the supratidal facies, whereas in the upper part of δ values and Sr contents drop sharply. Cyclic variations in evaporation and in meteoric water influence, determined from oxygen isotopic composition, reveal that the cyclicity of the beds containing the most limestones (supratidal) and those with the most marls (subtidal) is related to climatic changes. The coldest periods are those represented by supratidal deposits, when the sea level was at its lowest. During the warmest periods, when the overall sea level was higher, subtidal deposits accumulated in the region. A genetic model is proposed, according to which the asymmetrical sedimentary cycles occur in response to glacio-eustatic changes with a periodicity similar to that of Plio-Pleistocene sea-level variations, but with a much lower range due to the smaller extent of polar ice caps during the Early Cretaceous. The glacio-eustatic changes involved a rapid sea-level rise and a slow sea-level fall.  相似文献   

3.
《Gondwana Research》2001,4(3):377-386
The Kerala Khondalite belt is a Proterozoic metasupracrustal granulite facies terrain in southern India comprising garnet-biotite gneiss, garnet-sillimanite gneiss and orthopyroxene granulites as major rock types. Calc-silicate rocks and marbles, occurring as minor lithologies in the Kerala Khondalite Belt, show different mineral assemblages and reaction histories of which indicate a metamorphic P-T-fluid history dominated by internal fluid buffering during the peak metamorphism, followed by external fluid influx during decompression. The carbon and oxygen isotopic compositions of calcite from three representative metacarbonate localities show contrasting evolutionary trends. The Ambasamudram marbles exhibit carbon and oxygen isotope ratios (δ13C ∼ 0‰ and δ18O ∼ 20‰) typical of middle to late Proterozoic marine carbonate sediments with minor variation ascribed to the isotopic exchange due to the devolatilization reactions. The δ13C and δ18O values of ∼ −9‰ and 11‰, respectively, for calcite from calc-silicate rocks at Nuliyam are considerably low and heterogeneous. The wollastonite formation here, possibly corresponds to an earlier event of fluid infiltration during prograde to peak metamorphism, which resulted in decarbonation and isotope resetting. Further, petrologic evidence supports a model of late carbonic fluid infiltration that has partially affected the calc-silicate rocks, with subsequent isotope resetting, more towards the contact between calc-silicate rock and charnockite. At Korani, only oxygen isotopes have been significantly lowered (δ18O ∼ 13‰) and the process involved might be a combination of metamorphic devolatilization accompanied by an aqueous fluid influx, supported by petrologic evidence. The stable isotope signatures obtained from the individual localities, thus indicate heterogeneous patterns of fluid evolution history within the same crustal segment.  相似文献   

4.
Variations of carbon and oxygen isotopic ratios in response to cyclical sea level fluctuations have been documented from a Paleoproterozoic peritidal stromatolite succession. The upper division of the Kajrahat Limestone, Vindhyan Supergroup of central India consists of several shallowing upward stromatolite cycles identified by regular and systematic changes in stromatolite size. Normally, larger stromatolites are followed upward in the succession by smaller stromatolites and microbial laminites that occupy the top of the cycle. Desiccation cracks are found in all the facies indicating subaerial exposure. We investigated the stable isotope compositional variations across nine complete stromatolite cycles showing frequent subaerial emergence. Carbon and oxygen isotopic values of the limestones, in general, are comparable to contemporary marine values available from earlier studies but show regular depletion in response to shallowing of the water level. The δ13C and δ18O values of the limestones vary within an individual stromatolite cycle; depleted values characterize the topmost part of the cycles. The isotope pattern is explained by micritic carbonate deposition in different sub environments of the shallow marine domain having different salinity and variable duration of exposure. These variations also probably caused the observed scatter in δ13C and δ18O values of supratidal microbial laminites.  相似文献   

5.
Purbeckian (lowermost Cretaceous) peritidal carbonates are characterized by open marine, lagoonal, intertidal and lacustrine facies arranged in Milankovitch-type shallowing upward sequences. Shallowing upward sequences typically consist of 2–6 individual beds. The sequences may be (i) complete, (ii) incomplete or (ii) pedogenetically overprinted, reflecting the duration of subaerial exposure and/or the extent of erosion and pedogenetic modification at the cycle tops. The stable isotopic composition of the peritidal micrites reveals homogenous δ18O values attributed to diagenetic stabilization in a meteoric, water-buffered system. Carbon isotopes show three distinctly different carbon isotope patterns dependent on the completeness of the shallowing upward sequences. Complete shallowing upward sequences consist of 4–6 individual carbonate beds. The carbon isotope values show a facies-dependent pattern: open marine carbonate muds record enriched δ13C values of +0·28‰ while lagoonal (−0·82‰), intertidal (−2·46‰) and lacustrine micrites (−2·96‰) are increasingly depleted. This distinct pattern is explained by carbonate mud deposition in environments of differing salinity and marine influence. Incomplete sequences (2–5 carbonate beds) are characterized by depleted δ13C values below subaerial exposure surfaces that become progressively enriched in 13C with increasing depth. Pedogenetically overprinted sequences (1–3 carbonate beds) show strong 13C depletion throughout the sequence with little variation in the carbon isotopic composition. The depleted values (−4·5‰) of the pedogenetically altered micrites suggest that modification during subaerial exposure was associated with equilibration with meteoric solutions enriched in isotopically light soil gas CO2. The duration of subaerial exposure is the most crucial factor determining the extent of pedogenetic alterations, the completeness of the shallowing upward sequences and the carbon isotope pattern. The recorded patterns clearly illustrate that micrites have a good potential for the preservation of their primary carbon isotopic composition if the duration of subaerial exposure is rather brief. Otherwise, the recorded carbon isotope patterns may support sequence stratigraphic analysis by providing a refinement of the time-stratigraphic interpretation.  相似文献   

6.
Hydrothermal convection initiated by emplacement of the gabbro-syenite complex of Abu Khruq into the Egyptian basement 89 Ma ago systematically altered the trace element and isotopic compositions of the syenites. The scale of Sr transport in migrating solutions was far larger than the scale of Sr isotopic equilibration within rocks. As a result, Sr exchange was heterogeneous in the syenites, an effect which can be observed on three different scales. Within grains of a single mineral species, heterogeneities are related to grain boundaries and microfractures through which fluids migrated. Among minerals within rock samples, heterogeneities are related to differences in susceptibility to Sr alteration. Among samples within a single unit, heterogeneous alteration is apparently related to differences in permeability close to fracture zones.During the early stages of alteration radiogenic Sr derived from the country rocks was added to the syenites, causing small net changes in concentration (5 ppm ave.). Some Rb-Sr mineral isochrons from single rock samples yield the emplacement age because isotopic equilibration of this added Sr sometimes occurred within rock specimens. However, regressions of the whole-rock Rb-Sr data yield apparent ages that are about 10 Ma too old. Later stage alteration involved larger changes in whole-rock Sr concentration (45 ppm ave.) but had little further effect on the isotopic relationships because the Sr was derived from cogenetic gabbros rather than the country rocks.Alterations of Rb, Sr, and Sr isotopic compositions are not well correlated with changes in 18O/16O ratio because mineralogy played an important role in decoupling trace element and oxygen isotopic alteration. In general, the absence of such correlations for whole-rock data is not diagnostic of rocks with unaltered trace element and isotopic compositions. Mineral-scale Sr isotopic heterogeneities associated with grain boundaries and microfractures may be the most unambiguous evidence of trace element mobility.Deceased on 9/81  相似文献   

7.
Nodular chert from the middle and upper Arbuckle Group (Early Ordovician) in the Slick Hills, SW Oklahoma, was formed by selective replacement of grainstones, burrow fillings, algal structures, and evaporite nodules. Chert nodules are dominantly microquartz with minor fibrous quartz (both quartzine and chalcedony), megaquartz, and microflamboyant quartz. Lepisphere textures of an opal-CT precursor are preserved in many (especially in finely-crystalline) chert nodules. The δ18O values of microquartz chert range from +23.4 to + 28.80/00 (SMOW), significantly lower than those of Cenozoic and Mesozoic microquartz chert formed both in the deep sea and from near-surface sea water. The δ18O values of chert decrease with increasing quartz crystal size. Silicification in the Arbuckle Group occurred during early diagenesis, with the timing constrained by the relative temporal relationships among silicification, burial compaction, and early dolomite stabilization. Silica for initial chert nucleation may have been derived from both dissolution of sponge spicules and silica-enriched sea water. Chert nucleation appears to have been controlled by the porosity, permeability, and organic matter content of precursor sediments. This conclusion is based on the fact that chert selectively replaced both porous grainstones and burrows and algal structures enriched in organic matter. Growth of chert probably occurred by a maturation process from opal-A(?), to opal-CT, to quartz, as indicated by the presence of opal-CT precursor textures in many chert nodules. Although field and petrographic evidence argues for an early marine origin for chert in the Arbuckle Group, the light δ18O values are inconsistent with this origin. Meteoric resetting of the δ18O values of the chert during exposure of the carbonate platform best explains the light δ18O values because: (i) the δ18O values of chert nodules decrease with decreasing δ18O values of host limestones, and (ii) chert nodules from early dolomite, which underwent more extensive meteoric modification than associated limestones, have lighter δ18O values than chert nodules from limestones. Increasing recrystallization of chert nodules by meteoric water resulted in progressive 18O depletion and (quartz) crystal enlargement.  相似文献   

8.
Detailed information on semi‐arid, palustrine carbonate–calcrete lithofacies associations in a sheetwash‐dominated regolith setting is sparse. This is addressed by studying the Lower Limestone of the Lameta Beds, a well‐exposed Maastrichtian regolith in central India. The general vertical lithofacies assemblage for this unit comprises: (a) basal calcareous siltstones and marls with charophytes, ostracods and gastropods; (b) buff micritic limestones associated in their upper parts with calcretized fissure‐fill sandstones; (c) sheetwash as fissure‐fill diamictites and thin pebbly sheets, locally developed over a few metres; and (d) sandy, nodular, brecciated and pisolitic calcretes at the top. The sequence is ‘regressive’, with upsection filling of topographic lows by increased sheetwash. Lateral lithofacies change is marked, but there are no permanent open‐water lake deposits. In topographic lows close to the water table, marshy palustrine or groundwater calcretes formed, whereas on better drained highs, brecciation and calcretization occurred. Prolonged exposure is implied, suggesting that shrinkage was the main cause of brecciation. Evidence for rhizobrecciation and other biological calcrete fabrics is sparse, contrasting with the emphasis on root‐related brecciation in many studies of palustrine lithofacies. Stable isotope (δ18O and δ13C) values are consistent with the palustrine limestones being fed from meteoric‐derived groundwater with a strong input of soil‐zone carbon. There is overlap of both δ18O and δ13C values from the various palustrine and calcrete fabrics co‐occurring at outcrop. This suggests that, in groundwater‐supported wetlands, conversion from palustrine carbonate to calcrete need not show isotopic expression, as the groundwater source and input of soil‐zone carbon are essentially unchanged. Cretaceous–Tertiary δ18O and δ13C values from palustrine lithofacies and associated calcretes appear to be strongly influenced by the inherited values from lakes and wetlands. Hydrologically closed lakes and marine‐influenced water bodies tend to result in low negative palustrine δ18O and δ13C values. During brecciation and calcretization, the degree of isotopic inheritance depends on whether or not alteration occurs in waters that are different from those of the original water body or wetland. Marked biological activity (e.g. rhizobrecciation or root mat development) during calcretization may lower δ13C values where C3 plants are abundant but, in shrinkage‐dominated systems, δ13C values will be largely inherited from the palustrine limestones.  相似文献   

9.
Crystallization of anatectic melts in high-temperature metamorphic terrains releases volatile-rich magmas that can be transported into adjacent lithologies. This study addresses the variations in the oxygen, boron and hydrogen isotopic composition of aplite-pegmatite dikes that formed during the crystallization of anatectic melts in regional high-temperature metamorphism on the island of Naxos, Greece, and propagated upward into the overlying sequences of metamorphic schist. The transport distance of these dikes was increased through a significant horizontal component of travel that was imposed by contemporaneous low-angle extensional shearing. Laser fluorination oxygen isotope analyses of quartz, tourmaline, garnet, and biotite mineral separates from the aplite-pegmatite dikes show a progressive rise in δ18O values with increasing distance from the core. Oxygen isotope fractionations among quartz, tourmaline, and garnet show temperature variations from > 700°C down to ∼400°C. This range is considered to reflect isotopic fractionation beginning with crystallization at high temperatures in water-undersaturated conditions and then evolving through lower temperature crystallization and retrograde sub-solidus exchange. Two processes are examined for the cause of the progressive increase in δ18O values: (1) heterogeneous δ18O sources and (2) fluid-rock exchange between the aplite/pegmatite magmas and their host rock. Although the former process cannot be ruled out, there is as yet no evidence in the exposed sequences on Naxos for the presence of a suitable high δ18O magma source. In contrast, a tendency for the δ18O of quartz in the aplite/pegmatite dikes to approach that of the quartz in the metamorphic rock suggests that fluid-rock exchange with the host rock may potentially be an important process. Advection of fluid into the magma is examined based on Darcian fluid flow into an initially water-undersaturated buoyantly propagating aplitic dike magma. It is shown that such advective flow could only account for part of the 18O-enrichment, unless it were amplified by repeated injection of magma pulses, fluid recycling, and deformation-assisted post-crystallization exchange. The mechanism is, however, adequate to account for hydrogen isotope equilibration between dike and host rock. In contrast, variations in the δ11B values of tourmalines suggest that 11B/10B fractionation during crystallization and/or magma degassing was the major control of boron geochemistry rather than fluid-rock interaction and that the boron isotopic system was decoupled from that of oxygen.  相似文献   

10.
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   

11.
The Berriasian Rupelo Formation of the W Cameros Basin consists of a 2–200 m thickness of marginal and open lacustrine carbonate and associated deposits. Open lacustrine facies contain a non-marine biota with abundant charophytes (both stems and gyrogonites), ostracods, gastropods and rare vertebrates. Carbonate production was mainly biogenic. The associated marginal lacustrine (‘palustrine’) facies show strong indications of subaerial exposure and exhibit a wide variety of pedogenic fabrics. Silicified evaporites found near to the top of the sequence reflect a short hypersaline phase in the lake history. The succession was laid down in a low gradient, shallow lake complex characterized by wide fluctuations of the shoreline. Carbon and oxygen stable isotope analyses from the carbonates show non-marine values with ranges of δ13 from ? 7 to ? 11‰and δ18 from ? 3 to ? 7.5‰. Differences in the isotopic composition of open lacustrine carbonates are consistent with sedimentary evidence of variation in organic productivity within the lake. Analyses from the entire sample suite plot on a linear trend; isotopic compositions become lighter with increasing evidence of pedogenic modification. This suggests progressive vadose zone diagenesis and influence of meteoric waters rich in soil-derived CO2. The stable isotope data thus support evidence from petrography and facies relations that ‘palustrine’limestones form through pedogenic modification of lake carbonates.  相似文献   

12.
On the basis of the isotopic composition of water in the northern part of Epirus, Greece, from springs at different altitudes with well-defined recharge areas, the altitude effect on the δ18O value of groundwater is –0.142±0.003ö (100?m)–1 and is uniform over the entire study area. Using the δ18O composition of surface water and groundwaters, the contribution of Ioannina Lake and the channel draining the lake water to the Kalamas River to the recharge of springs and boreholes was confirmed and quantitatively defined. In contrast, the Voidomatis and Vikos Rivers are not sources for recharge of the big springs along their banks. However, water from the Aoos River does replenish the aquifer in the unconsolidated deposits underlying the plain of Konitsa. In addition, limestones of Senonian–Late Eocene ages, dolomites, and limestones of the "Vigles" facies are hydraulically interconnected, and the limestones of the "Pantokrator" facies are hydraulically isolated from the other carbonate formations.  相似文献   

13.
《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   

14.
The preservation of premetamorphic, whole-rock oxygen isotope ratios in Adirondack metasediments shows that neither these rocks nor adjacent anorthosites and gneisses have been penetrated by large amounts of externally derived, hot CO2-H2O fluids during granulite facies metamorphism. This conclusion is supported by calculations of the effect of fluid volatilization and exchange and is also independently supported by petrologic and phase equilibria considerations. The data suggest that these rocks were not an open system during metamorphism; that fluid/rock ratios were in many instances between 0.0 and 0.1; that externally derived fluids, as well as fluids derived by metamorphic volatilization, rose along localized channels and were not pervasive; and thus that no single generalization can be applied to metamorphic fluid conditions in the Adirondacks.Analyses of 3 to 4 coexisting minerals from Adirondack marbles show that isotopic equilibrium was attained at the peak of granulite and upper amphibolite facies metamorphism. Thus the isotopic compositions of metamorphic fluids can be inferred from analyses of carbonates and fluid budgets can be constructed.Carbonates from the granulite facies are on average, isotopically similar to those from lower grade or unmetamorphosed limestones of the same age showing that no large isotopic shifts accompanied high grade metamorphism. Equilibrium calculations indicate that small decreases in 18O, averaging 1 permil, result from volatilization reactions for Adirondack rock compositions. Additional small differences between amphibolite and granulite facies marbles are due to systematic lithologie differences.The range of Adirondack carbonate 18O values (12.3 to 27.2) can be explained by the highly variable isotopic compositions of unmetamorphosed limestones in conjunction with minor 18O and 13C depletions caused by metamorphic volatilization suggesting that many (and possibly most) marbles have closely preserved their premetamorphic isotopic compositions. Such preservation is particularly evident in instances of high 18O calcites (25.0 to 27.2), low 18O wollastonites (–1.3 to 3.5), and sharp gradients in 18O (18 permil/15m between marble and anorthosite, 8 permil/25 m in metasediments, and 6 permil/1 m in skarn).Isotopic exchange is seen across marble-anorthosite and marble-granite contacts only at the scale of a few meters. Small (<5 m) marble xenoliths are in approximate exchange equilibrium with their hosts, but for larger xenoliths and layers of marble there is no evidence of exchange at distances greater than 10 m from meta-igneous contacts.  相似文献   

15.
Interstitial solution was recovered from core samples of a borehole through 472 m of the Upper Cretaceous Chalk formation in eastern England. The solution has been analysed for major and some minor components and also for oxygen and hydrogen isotopic composition. Samples of the carbonate rock have also been analysed following acid dissolution. The general feature of interstitial solution chemistry is a progressive dilution of dissolved species with decreasing depth, from a near-marine composition found in the deepest samples which are identified as connate water. Departures from the expected dilution trend are interpreted as evidence for diagenetic reactions during burial or as a result of freshwater circulation following subaerial uplift. Sr2+, Li+ and F? have been enriched in interstitial solution and K+ has been slightly depleted. The profile of chalk chemistry with depth shows no conclusive evidence for changes in the Mg and Sr content of the bulk carbonate due to freshwater diagenesis. The δ18O and δD of the interstitial water reflect the same mixing as that shown by dissolved species. However an apparent depletion of 18O and D in the deepest fluids with respect to the expected marine isotopic composition is tentatively explained as a result of the differences in diffusion rates of aqueous oxygen and hydrogen and of ionic solutes.  相似文献   

16.
Dolomites occur extensively in Cambrian to Lower Ordovician carbonates in the Tienshan orogen of the Quruqtagh area, north‐east Tarim Basin, where thick (up to 1 km), dark grey lenticular limestones of semi‐pelagic to pelagic origin are prominent. The dolomites generally occur as beige, anastomosed geobodies that cross‐cut well‐stratified limestones. Based on detailed field investigations and petrographic examination, three types of matrix dolomite are identified: fine crystalline planar‐e (Md1), fine to medium crystalline planar‐s (e) (Md2) and fine to coarse crystalline non‐planar‐a (Md3) dolomites. One type of cement dolomite, the non‐planar saddle dolomite (Cd), is also common. The preferential occurrence of Md1 along low‐amplitude stylolites points to a causal link to pressure dissolution by which minor Mg ions were probably released for replacive dolomitization during shallow burial compaction. Type Md2, Md3 and Cd dolomites, commonly co‐occurring within the fractured zones, have large overlaps in isotopic composition with that of host limestone, implying that dolomitizing fluids inherited their composition from remnant pore fluids or were buffered by the formation water of host limestones through water–rock interaction. However, the lower δ18O and higher 87Sr/86Sr ratios of these dolomites also suggest more intense fluid–rock interaction at elevated temperature and inputs of Mg and radiogenic Sr from the host limestones with more argillaceous matter and possibly underlying Neoproterozoic siliciclastic strata. Secondary tensional faults and fractures within a compressional tectonic regime were probably important conduits through which higher‐temperature Mg‐rich fluids that had been expelled from depth were driven by enhanced tectonic compression and heating during block overthrusting, forming irregular networks of dolomitized bodies enclosed within the host limestones. This scenario probably took place during the Late Hercynian orogeny, as the Tarim block collided with Tienshan island arc system to the north and north‐east. Subsequent downward recharges of meteoric fluids into the dolomitizing aquifer probably terminated dolomitization as a result of final closure of the South Tienshan Ocean (or Palaeo‐Asian Ocean) and significant tectonic uplift of the Tienshan orogen. This study demonstrates the constructive role of notably tensional (or transtensional) faulting/fracturing in channelling fluids upward as a result of intense tectonic compression and heating along overthrust planes on the convergent plate margin; however, a relatively short‐lived, low fluid flux may have limited the dolomitization exclusively within the fractured/faulted limestones in the overthrust sheets.  相似文献   

17.
The Whitestone Anorthosite (WSA), located in the Central Gneiss Belt of the south-western Grenville Province, Ontario, exhibits a nearly concentric metamorphic envelope characterized by an increase in modal scapolite, hornblende, epidote and garnet, developed around a core of granulite facies clinopyroxene ± orthopyroxene ± garnet meta-anorthosite. Scapolite- and hornblende-bearing assemblages develop mainly at the expense of plagioclase and pyroxene within the envelope. Stable isotopic and petrological data for scapolite-bearing mineral assemblages within meta-anorthosite constrain the source of carbon responsible for CO3-scapolite formation and the extent of fluid/rock interaction between the anorthosite and adjacent lithologies. Stable isotopic data indicate increasing δ18O and δ13C from core to margin of the meta-anorthosite and for samples from the southern extension of the WSA, where it is ductilely deformed within the Parry Sound Shear Zone (PSSZ). The average δ18OSMOW value (whole rock) for the WSA core is 6.9‰, increasing to 11.5‰ where the WSA is in tectonic contact with marble breccia. The average δ13CPBD value of scapolite in meta-anorthosite from the centre of the WSA is -3.4‰, increasing to -0.5‰ at the eastern (marble) contact. Average values of δ13C for scapolite and whole-rock δ18O for samples from the shear zone are -1.0 and 8.0‰, respectively. Marbles have average δ18O and δ13C values of 19.2 and -0.4‰, respectively. The sulphate content of texturally primary scapolite decreases from the core of the WSA (XSO4= 0.48) to the eastern contact (≤0.05). Texturally late scapolite after plagioclase and garnet tends to be CO3-rich relative to texturally primary scapolite, and some scapolite grains show zoning in the anion site with CO3-enriched rims. Scapolite composition may vary at any scale from a single grain to outcrop. The pattern of isotopic enrichment in 13C and 18O preserved in the eastern margin of the WSA is consistent with marble as the major source of fluid contributing to the formation of the metamorphic envelope. The decrease in XSO4 and increase in XCO3 in scapolite toward the margin of the WSA indicate that the volatile content was reset by, or developed from, a CO2-bearing fluid. Assuming derivation of fluid from marble, minimum fluid/rock values at the margin of the WSA range from 0.03 for the least enriched, to 0.30 for the most isotopically enriched samples. Although marble is not found in immediate contact with samples of sheared meta-anorthosite from the PSSZ, a marble source is also consistent with the C and O isotope composition and anion chemistry of scapolite within these samples.  相似文献   

18.
Quartz-eye keratophyric tuffs at Aljustrel, S. Portugal, Iberian Pyrite Belt possess unusually high, uniform whole rock δ-values up to 18.1%. with a mean of 16.7 ± 0.7%.. Because the quartz eye cores have δ18O 12.0 to 13.5%. the felsic tuffs may have had an original whole rock oxygen isotope composition of 10 to 11%. The deduced enrichments of up to +8%. in keratophyric derivatives is attributed to isotope exchange with abundant marine water under temperatures which diminished to ≤ 100°C, during thermally driven convective cooling. The isotopic uniformity requires elevated permeability of ～ 10?8 cm2, such that the second critical Rayleigh number was exceeded, and drifting, non steady state convection cells dominated, with relatively smooth thermal structures.In mineralised counterparts of the tuffs beneath the Feitais-Estacao Zn-Pb-Cu massive sulphide orebodies, whole rock δ-values are ~12%. and quartz (13.3–15.4%.)-chlorite (3.2–6.3%.) fractionations correspond to temperatures of 220–270°C, and a calculated fluid δ18O of 1.4 to 5.7%. This local isotopic overprinting in vent domains of the regionally high 18O was induced by a stable, second stage convective regime imposed by drastic reduction of permeability accompanying capping of the geothermal discharge by hydrothermal cherts, and/or progressive spilitisation of the tuffs. At lower water/rock coupled with higher temperatures, the recirculating marine water underwent variable 18O enrichment up to 5.7%. by exchange with the high 18O tuffs. An upwards increase in δ18O quartz and δ-quartz reflects progressive cooling of the geothermal discharge from 15.4%. 270°C in the stockwork, through 18.3%. 220–240°C in the orebody, to 20.1%. 110–130°C in overlying hydrothermal cherts, probably induced by entrainment of ambient marine bottom water in sub-seafloor aquifers.  相似文献   

19.
REE distribution, strontium content and oxygen isotopic composition have been studied in the Lower Cretaceous dolomites and their interbedded and/or parental limestones of Central Tunisia. Dolomites, as indicated by previous sedimentologic, geochemical and isotopic study, are different in origin. Environments of dolomite formation include: evaporitic sabkha, deep phreatic, karst and lacustrine. With the exception of the sabkha environment, dolomitizing fluids presumably have been essentially meteoric. The comparison between REE distributions in dolomites and limestones clearly suggests that the general shapes of the REE patterns are preserved during dolomitization. Nevertheless, the total REE amounts are somewhat lowered in dolomites comparatively to parental limestones. Moreover, within the dolomites, the total REE contents are positively correlated to the Sr and δ18O contents; thus indicating that the decrease in REE, Sr, and δ18O contents is related to a decrease in the salinity of dolomitizing fluids. In addition, dolomites associated with emergence surfaces (karst) are the most impoverished in REE. Furthermore, they are relatively enriched in light REE, indicating a more or less important fractionation with the REE distributions. This enrichment has been related to the influence of the inorganic complexes which favours the greatest solubility of the heavy REE in basic solution with respect to the lightest members of the REE group.  相似文献   

20.
Oxygen isotope studies of the Suzhou granite have been made based on drill-hole samples. In the inner part, the δ18O values are less variable either in the whole-rock, quartz or in feldspar. Oxygen isotopic compositions are in equilibrium between coexisting quartz and feldspar. Data points from the inner part are plotted in a small area in the δ18OQ-δ18Of diagram, indicating that this part has not been affected by meteoric hydrothermal fluids. But the whole-rock δ18O values of the marginal part vary greatly. Oxygen isotopic compositions are in extreme disequilibrium between quartz and feldspar. Data points from the marginal part are displayed with a nearly vertical slope in the δ18OQ-δ18Of diagram, implying that rocks of this part are affected by the meteoric hydrothermal fluids. Extreme water-rock interactions lead to mineralizations of rare-elements (Nb, Ta, as well as Zr, Hf, Th) in the marginal part. Source materials of the Suzhou granite are also discussed in this paper.  相似文献   

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