High-¹⁸O granitic plutons from the Frontenac Axis,Grenville province of ontario,Canada     

Yuch-Ning Shieh 《Geochimica et cosmochimica acta》1985,49(1):117-123

  相似文献   

Etude systématique des isotopes de l'oxygène,du carbone et du strontium dans les carbonatites     

Françoise Pineau  Marc Javoy  Claude J Allegre 《Geochimica et cosmochimica acta》1973,37(11):2363-2377

${}^{18}\text{O}{}^{16}\text{O}$, ${}^{13}\text{C}{}^{12}\text{C}$ and ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios have been measured on the same samples for carbonatite complexes. The results show that besides the ‘carbonatite box’ of Tayloret al. (1967) there exist higher δ¹⁸O and δ¹³C values than can be explained by late magmatic or deuteric processes. These processes correspond to high concentrations of CO₂ and lead to big enrichments in ¹⁸O and ¹³C as well as in some ‘volatile’ elements. Strontium results are consistent with a model of selective contamination of deep-seated material by highly radiogenic strontium. The whole study leads to the opinion that parent magmas of carbonatites differentiated in a crustal environment with or without significant contamination.  相似文献   

Hydrogen,oxygen and carbon isotopic evidence for the origin of rodingites in serpentinized ultramafic rocks     

David B. Wenner 《Geochimica et cosmochimica acta》1979,43(4):603-614

$\text{D}\text{H}$, ${}^{18}\text{O}{}^{16}\text{O}$ and ${}^{13}\text{C}{}^{12}\text{C}$ analyses were made of 14 whole rock and 28 mineral samples of rodingites associated dominantly with lizardite-chrysotile serpentinites from the West Coast of the U.S.A., New Zealand, and the Northern Appalachian Mtns. The δD values of the rodingite minerals are in three groupings: 5 monomineralic veins of pectolite, ?281 to ?429; 8 monomineralic veins of xonotlite, ?112 to ?135; all other minerals, including hydrogarnet, idocrase, prehnite, actinolite, nephrite, and chlorite, ?34 to ?80. Most calcites in rodingites have δ¹⁸O (+9.3 to +14.4) and (δ¹³C (?6.7 to +0.9) values similar to calcites in other Franciscan rocks, but distinct from the very low temperature calcite veins in serpentinites. The $\text{D}\text{H}$ data, combined with δ¹⁸O values of xonotlite (+5.7 to +10.9) and pectolite (+8.9 to +12.4) suggest formation from meteoric-type waters at low temperatures; the $\text{D}\text{H}$ depletion of pectolite, however, is anomalous. Rodingite whole rock values range from δ¹⁸O = +4.1 to +11.5 and δD = ?50 to ?86; one sample containing minor amounts of lizardite-chrysotile serpentinite has δD = ?92, outside this range. However, most rodingites of basaltic or gabbroic parentage are more restricted in δ¹⁸O (+4.1 to +8.6). Such a wide range in δ¹⁸O is consistent with the idea that most rodingites form over a relatively broad range of hydrothermal temperatures. Hydrogen isotopic data for most rodingite minerals (except xonotlite and pectolite) and for whole rocks are suggestive of non-meteoric waters. These $\text{D}\text{H}$ data overlap those observed for veins of hydrous minerals found in Franciscan igneous rocks studied by Margaritz and Taylor (1976, Geochim. Cosmochim. Acta40, 215–234), possibly suggesting evolved D-enriched, connate type metamorphic waters generated during high P, low T Franciscan-type metamorphism at temperatures (250–500°C) comparable to estimates based on mineral stabilities. Such an interpretation is supported by the ${}^{18}\text{O}{}^{16}\text{O}$ and ${}^{13}\text{C}{}^{12}\text{C}$ data for calcite in rodingites.The isotope data appear to contradict some of the conclusions derived from geologic and petrologic studies that indicate concomitant metasomatism and serpentinization of their presently observed host rock. These data appear most consistent with the interpretation that most rodingite minerals, with the exception of late-stage veins of xonotlite and possibly pectolite, may involve metasomatism in association with antigorite serpentinization of ultramafic rock. Subsequent upward tectonic transport in many instances may result in incorporation of the rodingites into their presently observed lizarditechrysotile host rock during or subsequent to pervasive shallow level serpentinization by meteoric waters.  相似文献   

O18O16 of feldspars in carbonate rocks     

J.R Lawrence  M Kastner 《Geochimica et cosmochimica acta》1975,39(2):97-102

Six authigenic feldspars and three detrital feldspars in limestones and dolostones of Eocene to Preeambrian ages were analyzed for their $\text{O}{}^{18}\text{O}{}^{16}$ content. The difference in δO¹⁸ between the authigenic feldspars (δO¹⁸range = + 18.2 to + 24.7%.) and carbonate host rocks, both limestones and dolostones, was found to be ?0.5 to ?1.4%. Detrital feldspars (δO¹⁸ = + 11.2, + 22.5 and + 17.0%.) exhibit Δ^feldspar_carbonate values of ?12.0, ?2.4 and ?1.6‰, respectively, and appear to have undergone increased isotopic exchange as a function of decreased grain size under solid-state conditions.  相似文献   

The formation of caliche in soils of the Mojave Desert,California     

William H. Schlesinger 《Geochimica et cosmochimica acta》1985,49(1):57-66

Radiocarbon and ²³⁰Th-²³⁴U dates of calcic horizons from calciorthid soil profiles in the Mojave Desert were used to calculate the rate of deposition of pedogenic CaCO₃. A major period of CaCO₃ deposition appears to have occurred about 20000 yBP forming calcic horizons below 100-cm depth during a climatic regime with greater effective rainfall than in the present. The overall rate of deposition has been 1.0 to 3.5 g CaCO₃/m²/yr during soil formation. This rate is consistent with present-day rates, assuming that the atmospheric deposition of Ca limits the process. Stable isotope ratios in calcic horizons indicate that CaCO₃ precipitated from a soil environment with CO₂ of ? 15.5%. ${}^{13}\text{C}{}^{12}\text{C}$ (vs. PDB) and H₂O of + 2.0%. ${}^{18}\text{O}{}^{16}\text{O}$ (vs. SMOW). These values suggest that CaCO₃ precipitates when seasonal drought simultaneously lowers soil pore pCO₂ and enriches soil water ¹⁸O by evaporation. The role of soil calcic horizons in the global geochemical cycle of carbon is discussed.  相似文献   

The marine oxygen isotope record in Pleistocene coral,Barbados, West Indies     

Richard G. Fairbanks  R.K. Matthews 《Quaternary Research》1978,10(2):181-196

The reef-crest coral Acropora palmata from late Pleistocene reefs on Barbados has recorded the same global variations in oxygen isotopes as planktonic and benthonic foraminifera. Although the record of oxygen isotopes in Acropora palmata is discontinuous, it offers several advantages over the isotope records from deep-sea sediments: (1) the coral grows at water depths of less than 5 m; (2) the samples are unmixed; (3) specimens may be sampled from various elevations of paleo-sea level; and (4) aragonitic corals are suitable for ${}^{230}\text{Th}{}^{234}\text{U}$ and $\text{He}\text{U}$ dating techniques. The latter advantage means that direct dating of the marine oxygen isotope record is possible. Oxygen isotope stage 5e corresponds to Barbados III, dated at 125,000 ± 6000 yr BP. Petrographic and geochemical evidence from five boreholes drilled into the south coast of Barbados indicates a major eustatic lowering (greater than 100 m below present sea level) occurred between 180,000 and 125,000 yr BP. The age and isotopic data suggest correlation of this change in sea level to Emiliani's oxygen isotope stage 6. Acropora palmata deposited at various elevations of sea level during oxygen isotope stage 6 vary by 0.11 ‰ δ¹⁸O for each 10 m of change in sea level. We further hypothesize a minimum drop of 2°C in the average temperature occurred during the regressive phase of oxygen isotope stage 6. These data indicate that temperature lowering of surface water near Barbados lagged behind a major glacial buildup during this time period. Using the δ¹⁸O vs sea level calibration herein derived, we estimate the relative height of sea stands responsible for Barbados coral reef terraces in the time range 80,000 to 220,000 yr BP.  相似文献   

Stable isotopic investigations of early development in extant and fossil chambered cephalopods I. Oxygen isotopic composition of eggwater and carbon isotopic composition of siphuncle organic matter in Nautilus     

Kimberley C. Crocker  Michael J. DeNiro  Peter D. Ward 《Geochimica et cosmochimica acta》1985,49(12):2527-2532

Eggwaters from the chambered cephalopod Nautilus are depleted in both ¹⁸O and deuterium relative to ambient seawater. Eggwaters from six other species, including the related chambered cephalopod Sepia, do not show such depletion. These observations indicate that the previously observed step towards more positive $\text{δ}{}^{18}\text{O}$ values in calcium carbonate laid down after Nautilus hatches, relative to carbonate precipitated prior to hatching, can be explained by equilibration of the carbonate with water in the egg before hatching and with seawater after hatching. The presence of an oxygen isotope difference between eggwater and seawater for Nautilus and its absence for Sepia suggest that hatching will be recorded in the $\text{δ}{}^{18}\text{O}$ values of shell carbonates for some but not all extinct and extant chambered cephalopods.The $\text{δ}{}^{13}\text{C}$ values of the organic fraction of the siphuncle in Nautilus do not show any consistent pattern with regard to the time of formation before or after hatching. This observation suggests that the minimum in $\text{δ}{}^{13}\text{C}$ values previously observed for calcium carbonate precipitated after Nautilus hatches is not caused by a change in food sources once the animal becomes free-swimming, as has been suggested.  相似文献   

Carbon and oxygen isotopes in epigenetic hydrothermal rocks from Hamam-el-Farun,Sinai     

Mordechai Magaritz  Arie Issar 《Chemical Geology》1973,12(2):137-146

Rock samples from an Eocene cliff above the thermal spring of Hamam-el-Farun (west coast of Sinai) show various degrees of dolomitization and calcitization ${}^{18}\text{O}{}^{16}\text{O}$ and ${}^{13}\text{C}{}^{12}\text{C}$ ratios indicate that dolomite and secondary calcite precipitated from hot brines.  相似文献   

Aragonite from deep sea ultramafic rocks     

E. Bonatti  J.R. Lawrence  P.R. Hamlyn  D. Breger 《Geochimica et cosmochimica acta》1980,44(8):1207-1214

Aragonite mineralization was observed in serpentinized peridotites from the Romanche and Vema Fracture Zones in the Atlantic and the Owen Fracture Zone in the Indian Ocean, either in veins or as radial aggregates in cavities within the serpentinites. Evidence of incipient dissolution of the aragonite crystals was observed in one case. The aragonites tend to have lower Mg content (< 0.03%) and higher Sr content (> 0.95%) relative to other marine aragonites. Their ${}^{18}\text{O}{}^{16}\text{O}$, ${}^{13}\text{C}{}^{12}\text{C}$ and ${}^{87}\text{Sr}{}^{86}\text{Sr}$ isotopic ratios suggest the aragonite was deposited at ocean floor temperatures from solutions derived from sea water circulating in fissures and fractures within the ultramafic rocks. The ${}^{18}\text{O}{}^{16}\text{O}$ ratios of the serpentines indicate serpentinization occurred at higher temperatures, probably deeper in the crust. Low-T reactions between circulating seawater and Mg-silicates (primarily serpentine and pyroxenes) caused high pH and enrichment of Mg and Ca in the solution, conditions favoring carbonate precipitation. Aragonite was formed rather than calcite presumably because the high Mg²⁺ concentration in the solution inhibited calcite precipitation. The high Sr content of the aragonites is probably related, at least in part, to their low temperature of formation. Opaque mineral grains containing over 8% NiO and over 40% MnO were observed concentrated along the margins of some of the aragonite veins, suggesting that Ni is one of the elements mobilized during reactions between ultramafic rocks and circulating seawater.  相似文献   

The extent of oxygen isotope exchange between clay minerals and sea water     

Hsueh-Wen Yeh  Samuel M. Savin 《Geochimica et cosmochimica acta》1976,40(7):743-748

The extent of oxygen isotopic exchange between detrital clay minerals and sea water was investigated by analyzing $\text{O}{}^{18}\text{O}{}^{16}$ ratios of separated fine-grained size fractions of deep-sea sediments from three North Pacific ocean cores. Isotopic results were interpreted according to models based on the assumption that the extent of isotopic exchange should increase with decreasing particle size and increasing time of exchange between the sediment and sea water. The data indicate that information concerning the provenance and mode of formation of detrital clay minerals can be obtained from the $\text{O}{}^{18}\text{O}{}^{16}$ ratios of the coarser-than-0.1 μm fraction of deep-sea sediments younger than several million years and the finer-than-0.1 μm fraction of deep-sea sediments younger than several tens of thousands of years. Furthermore, if the extent of chemical reaction between detrital clays and sea water is similar to the extent of oxygen isotopic exchange, such reaction may be important in regulating the chemistry of sea water.  相似文献   

Oxygen-isotope variations in sulfate ions in the water of some Italian lakes     

Gianni Cortecci 《Geochimica et cosmochimica acta》1973,37(6):1531-1542

The results obtained by measuring the sulfate content and its $\text{O}{}^{18}\text{O}{}^{16}$ ratios through time in some volcanic, tectonic and dam Italian lakes are reported here. The variations with time of the oxygen isotopic composition of the lake waters are also reported. The measurements refer mainly to surface water; however, a few deep samples were also studied.In the case of all the lakes examined, the variations with time of the oxygen isotopic composition and of the concentration of the dissolved sulfate cannot be explained in terms of the addition and of seasonal variations of the O¹⁸ content of rainwater sulfate. Biological redox processes involving bacterial reduction of sulfate and sulfide oxidation can reasonably account for the results obtained.According to Lloyd (1967), when sulfate is formed by bacterial sulfide oxidation, 68 per cent of the sulfate oxygen is water oxygen, while 32 per cent is dissolved molecular oxygen. The isotopic enrichment of the dissolved molecular oxygen in the lake waters relative to the isotope content of the atmospheric oxygen is mainly related to the biological activity in the waters.Assuming that a stagnation period takes place during summer and fall while a period of strong bio-respiratory activity takes place during winter and spring, it follows that a small isotope fractionation effect on molecular dissolved oxygen can be expected during stagnation while a high isotope fractionation can be expected during winter and spring. The O¹⁸ content of the sulfate dissolved in volcanic and tectonic lakes varies according to this hypothesis. The fact that similar O¹⁸ contents of the dissolved sulfate are or are not found in the same period of different years is probably related to similarities or differences in the climatic conditions.The bio-physical behaviour of the Corbara dam lake is different from that of other lakes. However, because of the continuous feeding by the Tiber River, variations of the sulfate concentration and its oxygen isotopic composition can be caused by the contribution of polluted water.  相似文献   

The geochemical evolution of the Pleistocene Lake Lisan-Dead Sea system     

Amitai Katz  Yehoshua Kolodny  Arie Nissenbaum 《Geochimica et cosmochimica acta》1977,41(11):1609-1626

The geochemical history of Lake Lisan, the Pleistocene precursor of the Dead Sea, has been studied by geological, chemical and isotopic methods.Aragonite laminae from the Lisan Formation yielded (equivalent) Sr/Ca ratios in the range 0.5 × 10^?2?1 × 10^?2, Na/Ca ratios from 3.6 × 10^?3 to 9.2 × 10^?3, $\text{δ}{}^{18}\text{O}{}_{\mathrm{PDB}}$ values between 1.5 and 7%. and $\text{δ}{}^{13}\text{C}{}_{\mathrm{PDB}}$ from ?7.7 to 3.4%..The distribution coefficient of Na⁺ between aragonite and aqueous solutions, $\text{λ}{}^{\mathrm{A}}{}_{\mathrm{Na}}$, is experimentally shown to be very sensitive to salinity and nearly temperature independent. Thus, Na/Ca in aragonite serves as a paleosalinity indicator.Sr/Ca ratios and $\text{δ}{}^{18}\text{O}$ values in aragonite provide good long-term monitors of a lake's evolution. They show Lake Lisan to be well mixed, highly evaporated and saline. Except for a diluted surface layer, the salinity of the lake was half that of the present Dead Sea (15 vs 31%).Lake Lisan evolved from a small, yet deep, hypersaline Dead Sea-like, water body. This initial lake was rapidly filled-up to its highest stand by fresh waters and existed for about 40,000 yr before shrinking back to the present Dead Sea. The chemistry of Lake Lisan at its stable stand represented a material balance between a Jordan-like input, an original large mass of salts and a chemical removal of aragonite. The weighted average depth of Lake Lisan is calculated, on a geochemical basis, to have been at least 400, preferably 600 m.The oxygen isotopic composition of Lake Lisan water, which was higher by at least 3%. than that of the Dead Sea, was probably dictated by a higher rate of evaporation.Na/Ca ratios in aragonite, which correlate well with $\text{δ}{}^{13}\text{C}$ values, but change frequently in time, reflect the existence of a short lived upper water layer of varying salinity in Lake Lisan.  相似文献   

Intensive sampling of noble gases in fluids at Yellowstone: I. Early overview of the data; regional patterns     

B.M. Kennedy  M.A. Lynch  J.H. Reynolds  S.P. Smith 《Geochimica et cosmochimica acta》1985,49(5):1251-1261

The Roving Automated Rare Gas Analysis (RARGA) lab of Berkeley's Physics Department was deployed in Yellowstone National Park for a 19 week period commencing in June, 1983. During this time 66 gas and water samples representing 19 different regions of hydrothermal activity within and around the Yellowstone caldera were analyzed on site. Routinely, the abundances of five stable noble gases and the isotopic compositions of He, Ne, and Ar were determined for each sample. In a few cases the isotopes of Kr and Xe were also determined and found to be of normal atmospheric constitution.Correlated variations in the isotopic compositions of He and Ar can be explained within the precision of the measurements by mixing of only three distinct components. The first component is of magmatic origin and is enriched in the primordial isotope ³He with ${}^3\text{He}{}^4\text{He}\text{≥ 16}$ times the air value. This component also contains radiogenic ⁴⁰Ar and possible ³⁶Ar with ${}^{40}\text{Ar}{}^{36}\text{Ar}\text{≥ 500}$, resulting in a ${}^3\text{He}{}^{36}\text{Ar}$ ratio ≥ 41,000 times the air value. The second component is assumed to be purely radiogenic ⁴He and ⁴⁰Ar (${}^{41}\text{He}{}^{401}\text{Ar}\text{= 4.08 ± .33}$). This component is the probable carrier of observed excesses of ²¹¹Ne, attributed to the α,n reaction on ¹⁸O. Its radiogenic character implies a crustal origin in U. Th, and Krich aquifer rocks. The third component, except for possible mass fractionation, is isotopically indistinguishable from the noble gases in the atmosphere. This component originates largely from infiltrating run-off water saturated with atmospheric gases.In addition to exhibiting nucleogenic ²¹¹Ne, Ne data show anomalies in the ratio ${}^{20}\text{Ne}{}^{20}\text{Ne}$, which correlate roughly with the ${}^{21}\text{Ne}{}^{22}\text{Ne}$ anomalies for the most part, but not as would occur from simple mass fractionation. Some exaggerated instances of the ${}^{20}\text{Ne}{}^{22}\text{Ne}$ anomaly occur which could be explained by combined mass fractionation of Ne and Ar isotopes to a severe degree coupled with remixing with normally isotopic gases. Otherwise exotic processes have to be invoked to explain the ²⁰Ne data.Relative abundances of the non-radiogenic and non-nucleogenic noble gases (²²Ne, ³⁶Ar, ⁸⁴Kr, and ¹³²Xe) are highly variable but strongly correlated. High Xe/Ar ratios are always accompanied by low Ne/ Ar ratios and vice versa. Except for water from the few cold (T < 20°C) springs analyzed, none of the samples have relative abundances consistent with air saturated water and the observed variations are not readily explained by the distillation of air saturated water.In characterizing each area of hydrothermal activity by the highest ${}^3\text{He}{}^4\text{He}$ ratio found for that area, we find that within the caldera this parameter is somewhat uniform at ~7 ± 1 times the air value. There are exceptions, most notably at Mud Volcano, an area located along a crest of recent and rapid uplift. Here the maximum ${}^3\text{He}{}^4\text{He}$ ratio is ~ 16 times the air value. Also noteworthy is Gibbon Basin which is in the vicinity of the most recent rhyolitic volcanism and exhibits a ${}^3\text{He}{}^4\text{He}$ ratio ~ 13 times the air value. Immediately outside the caldera the maximum $\text{sol}{}^3\text{He}{}^4\text{He}$ ratio decreases rapidly to values < ~3 times the air value.  相似文献   

Pollen and oxygen isotope analyses on late- and post-glacial sediments of the Tourbière de Chirens (Dauphiné, France)     

U. Eicher  U. Siegenthaler  S. Wegmüller 《Quaternary Research》1981,15(2):160-170

The sequence of vegetation phases in the late Glacial was studied in a sediment section from the bog Tourbière de Chirens by means of pollen analysis. ${}^{18}\text{O}{}^{16}\text{O}$ ratios of samples of lacustrine marl, obtained from the same profile, reflect variations of ${}^{18}\text{O}{}^{16}\text{O}$ in precipitation and thus provide an additional, independent paleoclimatic record. The observed ${}^{18}\text{O}{}^{16}\text{O}$ variations agree well with the climatic history as deduced from pollen analysis. The climatic transition from the Oldest Dryas to the Bølling period sensu lato, as well as the beginning and end of the Younger Dryas cold phase, is marked by abrupt changes in the ${}^{18}\text{O}{}^{16}\text{O}$ ratio which were observed also in other regions of the Alps. These drastic climatic changes probably took place simultaneously over large areas of Central Europe and occurred within short time spans.  相似文献   

Hydrogen and carbon isotopes of petroleum and related organic matter     

Hsueh-Wen Yeh  Samuel Epstein 《Geochimica et cosmochimica acta》1981,45(5):753-762

$\text{D}\text{H}$ and ${}^{13}\text{C}{}^{12}\text{C}$ ratios were measured for 114 petroleum samples and for several samples of related organic matter. δD of crude oil ranges from ?85 to ?181‰, except for one distillate (?250‰) from the Kenai gas field; δ¹³C of crude oil ranges from ?23.3 to ?32.5‰, Variation in δD and δ¹³C values of compound-grouped fractions of a crude oil is small, 3 and 1.1%., respectively, and the difference in δD and δ¹³C between oil and coeval wax is slight. Gas fractions are 53–70 and 22.6–23.2‰ depleted in D and ¹³C, respectively, relative to the coexisting oil fractions.The δD and δ¹³C values of the crude oils appear to be largely determined by the isotopic compositions of their organic precursors. The contribution of terrestrial organic debris to the organic precursors of most marine crude oils may be significant.  相似文献   

Source rock-crude oil correlation by isotopic type-curves     

W.J. Stahl 《Geochimica et cosmochimica acta》1978,42(10):1573-1577

An isotopic type-curve has been defined based on the ${}^{13}\text{C}{}^{12}\text{C}$ ratios of the saturated, aromatic, heterocomponent (NOSs), and asphaltene fractions of crude oils. These fractions show ¹³C enrichments with increasing polarity or polarizability. This systematic pattern can be used to estimate the ${}^{13}\text{C}{}^{12}\text{C}$ ratio of the kerogen from which the oil had been generated. Genetically associated source rock oil pairs have been used to show that the difference between the measured and the estimated δ-values of kerogen is about ?0.5%., and between the δ-values of the kerogen and the asphaltene fraction is approximately +0.6%.  相似文献   

Coupling among the terrestrial sulfur,carbon and oxygen cycles: numerical modeling based on revised Phanerozoic carbon isotope record     

Manfred Schidlowski  Christian E Junge 《Geochimica et cosmochimica acta》1981,45(4):589-594

Numerical modeling of the terrestrial oxygen budget based on the revised δ¹³C_carb record by Veizeret al. (1980) has shown that total photosynthetic oxygen has varied between ±7% and ±10% of its average reservoir size (～3.2 × 10²² g) during the last 800 myr as a result of oscillations of the sedimentary reservoir of organic carbon. Calculated curves of oxygen evolution display a distinct minimum in the Early Paleozoic framed by two maxima in the Latest Proterozoic and the Mesozoic. The sympathetic relationship observed between the curves of total oxygen evolution and respective functions for the partial reservoir of sulfate-bound oxygen suggests that the O₂ required for an additional conversion of sulfide to sulfate was most probably provided by excess burial of organic carbon, the results of the modeling thus adding credence to current interpretations proposed for the negative correlation between the secular ${}^{13}\text{C}{}^{12}\text{C}$ and ${}^{34}\text{S}{}^{32}\text{S}$ trends.  相似文献   

Importance of alteration of volcanic material in the sediments of deep sea drilling site 323: chemistry, 18O16O and 87Sr86Sr     

J.R. Lawrence  J.I. Drever  T.F. Anderson  H.K. Brueckner 《Geochimica et cosmochimica acta》1979,43(4):573-588

A downhole decrease in ¹⁸O, Mg²⁺ and K⁺, an increase in Ca²⁺ and a low ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio of 0.7067 in the pore fluids of DSDP site 323 were caused principally by the alteration of volcanic material. These chemical and isotopic patterns were produced by the alteration, in order of decreasing importance of: a 60-m thick basal layer of volcanic ash; the underlying basalts; and igneous components in the 640-m thick upper sequence composed largely of terrigenous material. A significant portion of the alteration of the ash in the basal sequence must have occurred before the deposition of the upper sediments, perhaps under the influence of advecting solutions. The rest of the alteration occurred during the deposition of the thick upper sediments. Mass balance considerations and the low δ¹⁸O values of most of the alteration products suggest that much of the later alteration occurred progressively over the last 13 Myr. The principal alteration products were smectite, potassium feldspar, clinoptilolite and calcite.  相似文献   

Hydrogen and carbon isotopic ratios of the cellulose nitrate and saponifiable lipid fractions prepared from annual growth rings of a California redwood     

Donald W. Northfelt  Michael J. DeNiro  Samuel Epstein 《Geochimica et cosmochimica acta》1981,45(10):1895-1898

The $\text{D}\text{H}$ and ${}^{13}\text{C}{}^{12}$C ratios of the cellulose nitrate and saponifiable lipid fractions prepared from eleven annual growth rings of a California redwood were determined. The $\text{D}\text{H}$ ratios of the two fractions are related to one another for the annual rings in the sapwood portion of the tree, but not for those in the heartwood or in the wood undergoing the transition from sapwood to heartwood. No relationship was observed between the ${}^{13}\text{C}{}^{12}$ ratios of the two fractions. These results suggest that analysis of the hydrogen isotopic composition of the saponifiable lipid fractions in plants will provide information useful for climatic reconstruction provided the initial isotopic record has not been changed by subsequent physiological or diagenetic processes.  相似文献   

Late Pleistocene paleoclimates of North America as inferred from stable isotope studies of speleothems     

Russell S. Harmon  Peter Thompson  Henry P. Schwarcz  Derek C. Ford 《Quaternary Research》1978,9(1):54-70

Some speleothems (CaCO₃ cave deposits) can be demonstrated to have been formed in oxygen isotopic equilibrium with their parent seepage waters and thus a record of relative fluctuations in depositional temperature can be obtained from the δ¹⁸O variations in successive growth layers of such deposits. These temperature fluctuations reflect variations in the average annual air temperature at the surface above the cave, and therefore permit inference of past continental climate changes. Equilibrium deposits have been obtained from caves in San Luis Potosi, Bermuda, Kentucky, West Virginia, Iowa, and Alberta, ranging in age from 200,000 years BP to the present, as determined by ${}^{230}\text{Th}{}^{234}\text{>U}$ dating of the speleothems. The δ¹⁸O time curves for the six sites show the following synchronous climatic fluctuations: warm periods from 190 to 165 and from 120 to 100 Ka, at 60 and 10 Ka, and cold periods from 95 to 65 and from 55 to 20 Ka. The periods of thermal maxima correspond in time to the interglacial periods of the marine foraminiferal isotopic and faunal temperature records and to periods of high sea stand as observed from radiometric dating of raised coral reefs. Maxima and minima in insolation appear to be synchronous with this record as well.  相似文献