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1.
Nine marble horizons from the granulite facies terrane of southern India were examined in detail for stable carbon and oxygen isotopes in calcite and carbon isotopes in graphite. The marbles in Trivandrum Block show coupled lowering of δ13C and δ18O values in calcite and heterogeneous single crystal δ13C values (? 1 to ? 10‰) for graphite indicating varying carbon isotope fractionation between calcite and graphite, despite the granulite facies regional metamorphic conditions. The stable isotope patterns suggest alteration of δ13C and δ18O values in marbles by infiltration of low δ13C–δ18O‐bearing fluids, the extent of alteration being a direct function of the fluid‐rock ratio. The carbon isotope zonation preserved in graphite suggests that the graphite crystals precipitated/recrystallized in the presence of an externally derived CO2‐rich fluid, and that the infiltration had occurred under high temperature and low fO2 conditions during metamorphism. The onset of graphite precipitation resulted in a depletion of the carbon isotope values of the remaining fluid+calcite carbon reservoir, following a Rayleigh‐type distillation process within fluid‐rich pockets/pathways in marbles resulting in the observed zonation. The results suggest that calcite–graphite thermometry cannot be applied in marbles that are affected by external carbonic fluid infiltration. However, marble horizons in the Madurai Block, where the effect of fluid infiltration is not detected, record clear imprints of ultrahigh temperature metamorphism (800–1000 °C), with fractionations reaching <2‰. Zonation studies on graphite show a nominal rimward lowering δ13C on the order of 1 to 2‰. The zonation carries the imprint of fluid deficient/absent UHT metamorphism. Commonly, calculated core temperatures are > 1000 °C and would be consistent with UHT metamorphism.  相似文献   

2.
Strong contrasts in ambient isotope ratios and in diet suggest stable isotopes in the otoliths of oceanic fish can resolve water masses and geographic areas, promising a powerful multivariate approach for examining population structure and provenance. To test this, whole otoliths were taken from Patagonian toothfish (Dissostichus eleginoides) sampled off the Patagonian Shelf and South Georgia, on either side of a population boundary, and otolith δ18O and δ13C values were measured to see if they could distinguish South American-caught fish from those taken in the Antarctic. Values of otolith δ18O and δ13C predicted capture area with 100% success, validating their use for distinguishing provenance and corroborating the prior evidence of population isolation. Values of δ18O in the otoliths reflected ambient values as well as seawater temperature: low values in Patagonian Shelf fish were consistent with exposure to Antarctic Intermediate Water (AAIW), and high values in South Georgia fish were consistent with exposure to Circumpolar Deep Water (CDW). In contrast, differences in otolith δ13C appeared to reflect diet: relative depletion of otolith δ13C at South Georgia compared to the Patagonian Shelf were most likely linked to differences in sources of metabolic carbon, as well as δ13C in dissolved inorganic carbon (DIC) of seawater. These contrasting properties strongly suggest that stable isotopes can resolve the provenance of toothfish from Antarctic sampling areas that hitherto have been difficult to separate. These results show that, by using the chemistry recorded in otoliths, researchers can exploit biogeochemical variation in fully marine environments to examine the spatial ecology of oceanic fish.  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.
The results of isotope-geochemical studies of carbonates of different mineral types from manganese and host rocks of the Famennian manganiferous formation of Pai-Khoi are reported. Kutnahorite ores are characterized by δ13C values from–6.6 to 1.3‰ and δ18O from 20.0 to 27.4‰. Rhodonite–rhodochrosite rocks of the Silovayakha ore occurrence have δ13C from–5.2 to–2.9 and δ18O from 25.4 to 24.3‰. Mineralogically similar rocks of the Nadeiyakha ore occurrence show the lighter carbon and oxygen isotopic compositions: δ13C from–16.4 to–13.1 and δ18O from 24.8 to 22.5‰. Similar isotopic compositions were also obtained for rhodochrosite–kutnahorite rocks of this ore occurrence: δ13C from–13.0 to–10.4‰ and δ18O from 24.6 to 21.7‰. Siderorodochrosite ores differ in the lighter oxygen and carbon isotopic compositions: δ18O from 18.7 to 17.6‰ and δ13C from–10.2 to–9.3‰, respectively. In terms of the carbon and oxygen isotopic compositions, host rocks in general correspond to marine sedimentary carbonates. Geological-mineralogical and isotope data indicate that the formation of the manganese carbonates was related to the hydrothermal ore-bearing fluids with the light isotopic composition of oxygen and carbon dissolved in CO2. The isotopic features indicate an authigenic formation of manganese carbonates under different isotopegeochemical conditions.  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.
Multicellular animals first appeared on the earth during the Ediacaran period. However, the relationship between the abrupt biological evolution and environmental changes is still ambiguous. In order to examine seawater temperature and the carbon cycle through the Ediacaran, we analyzed the carbon and oxygen isotope compositions of carbonate rocks from drill cores from the Three Gorges area, South China. Importantly, the core samples include the Nantuo tillite, corresponding to the Marinoan glaciation, through the Doushantuo to the lower Dengying Fms. in ascending order.The δ13C profile displays five positive and five negative anomalies (PI-1 to 5 and NI-1 to 5), and the oxygen isotopes display very high absolute values around 0‰ with the highest at + 1.83‰. The combined δ18O and δ13C chemostratigraphies display both positive and negative correlations between the δ18O and δ13C values. The occurrence of the negative correlations supports the preservation of primary δ18O and δ13C values.The sample NI-4 has a negative correlation of the δ18O and δ13C excursions. The correlation supports a primary signature for both δ18O and δ13C variations. The positive δ18O excursion, accompanied by evidence of a eustatic sea-level fall, provides direct evidence for global cooling in the mid-Ediacaran; the 580 Ma Gaskiers Glaciation is a potential candidate for this global cooling event. The negative δ13C excursion was possibly caused by an increase in remineralization of dissolved organic carbon (DOC) due to enhanced continental weathering during the glaciation.Sample NI-5 is characterized by very low δ13C values, down to ? 10‰, corresponding to the Shuram-Wonoka-Pertatataka Excursion. The cause of the δ13C negative excursion is still not clear. However, a ubiquitous occurrence in excursions worldwide, and the lower δ13C values in deeper sections favor the enhancement of remineralization and respiration rather than secondary alteration, a restricted sea environment and lithification in coastal areas.  相似文献   

7.
Karst rocks from the Huanglong Formation exposed at the margin of the Eastern Sichuan Basin can be divided into four types:slightly corroded, moderately corroded porous, intensely corroded brecciated and intensely corroded and replaced secondary calcic karstic rocks. The carbon, oxygen and strontium isotope compositions of the various karst rocks are analyzed systematically and compared to rocks without karst corrosion. The results indicate that(1) the Huanglong Formation in the eastern Sichuan Basin was a restricted bay supplied and controlled by freshwater in which mudmicrite and mud-dolomicrite exhibit low δ13C and δ18O values and high 87Sr/86 Sr ratios;(2) all types of karstic rocks in the paleokarst reservoirs of the Huanglong Formation in the research area are affected by atmospheric freshwater with the δ13C and δ18O values and 87Sr/86 Sr ratios in the original formation approaching those of atmospheric freshwater, which reflects ancient hydrological conditions, fluid properties, isotopic source and the fractionation effect;(3) the intensely corroded and replaced secondary limestone is affected by a variety of diagenetic fluids, often reflected by δ13C and δ18O values, while the 87Sr/86 Sr ratios exhibit the strong degree of the corrosion;(4) after comparing the 87Sr/86 Sr ratios of each type of karst rock, the diagenetic fluids are determined to be mainly atmospheric freshwater, and depending on the strength of corrosion, and the low 87Sr/86 Sr ratio fluids in the layer will participate in the karst process. The carbon, oxygen, and strontium isotopes of different karstic reservoirs can provide meaningful geochemical information for forecasting and evaluating the development and distribution rules of the Huanglong Formation at the margin of the eastern Sichuan Basin in time and space.  相似文献   

8.
The Newania carbonatite complex of Rajasthan, India is one of the few dolomite carbonatites of the world, and oddly, does not contain alkaline silicate rocks thus providing a unique opportunity to study the origin and evolution of a primary carbonatite magma. In an attempt to characterize the mantle source, the source of carbon, and the magmatic and post-magmatic evolution of Newania carbonatites, we have carried out a detailed stable carbon and oxygen isotopic study of the complex. Our results reveal that, in spite of being located in a metamorphic terrain, these rocks remarkably have preserved their magmatic signatures in stable C and O isotopic compositions. The δ13C and δ18O variations in the complex are found to be results of fractional crystallization and low temperature post-magmatic alteration suggesting that like other carbonatites, dolomite carbonatites too fractionate isotopes of both elements in a similar fashion. The major difference is that the fractional crystallization of dolomite carbonatites fractionates oxygen isotopes to a larger extent. The modes of δ13C and δ18O variations in the complex, ?4.5?±?1‰ and 7?±?1‰, respectively, clearly indicate its mantle origin. Application of a multi-component Rayleigh isotopic fractionation model to the correlated δ13C versus δ18O variations in unaltered carbonatites suggests that these rocks have crystallized from a CO2 + H2O fluid rich magma, and that the primary magma comes from a mantle source that had isotopic compositions of δ13C ~ ?4.6‰ and δ18O ~ 6.3‰. Such a mantle source appears to be a common peridotite mantle (δ13C = ?5.0?±?1‰) whose carbon reservoir has insignificant contribution from recycled crustal carbon. Other Indian carbonatites, except for Amba Dongar and Sung Valley that are genetically linked to Reunion and Kerguelen plumes respectively, also appear to have been derived from similar mantle sources. Through this study we establish that dolomite carbonatites are generated from similar mantle source like other carbonatites, have comparable evolutionary history irrespective of their association with alkaline silicate rocks, and may remain resistant to metamorphism.  相似文献   

9.
依据实测的塔里木盆地麦盖提斜坡玉北地区41个碳酸盐岩碳氧同位素数据,结合岩石学方法,研究了碳氧同位素的组成、演化及其地质意义。数据显示,δ~(13) C值主要分布在-2.6‰~0.7‰,均值为-1.0‰;δ~(18) O值分布在-9.4‰~-3.5‰,均值为-6.9‰。玉北地区古盐度为118.39~126.34,平均为121.94。奥陶系碳酸盐岩淡水改造作用明显。碳氧同位素的组成和演化不但可以指示沉积环境,而且还与生物生产率以及古海平面变化呈正相关性:δ~(13) C的低值对应于局限台地台内滩亚相沉积环境;δ~(13) C的高值对应于开阔台地滩间海、台内滩亚相沉积环境。碳氧同位素组成还对成岩环境有明显响应:鹰山组δ~(13) C与δ~(18) O均向高负值偏移,表明经历过强烈的表生岩溶作用;蓬莱坝组δ~(13) C低—中负值,δ~(18) O表现为高负值,在白云岩储层中可见鞍状白云石及燧石,主要为深埋藏成岩环境;良里塔格组同位素特征为δ~(18) O高负值,δ~(13) C低正值,并且在进入埋藏岩溶阶段之前还经历过风化壳岩溶作用。  相似文献   

10.
The calcite fossils of the Derbyhaven Beds, Isle of Man, have δ13C values (+ 1·8 PDB) similar to modern, shallow-water marine skeletons, but the δ18O values (?6·1 PDB) are much lighter than modern skeletons. The light oxygen values indicate either re-equilibration with isotopically light water before cementation started, or Carboniferous sea water with δ18O of ?6‰. Aragonite dissolution was followed by precipitation of zoned calcite cement. In this cement, up to six intracrystalline zones, recognized in stained thin sections, show isotopic variation. Carbon varies from + 3-8 to + 1-2‰. and oxygen from ? 2-6 to ? 12-4‰. with decreasing age of the cement. This trend is attributed to increasing temperature and to isotopic evolution of the pore waters during burial. The zoned calcite is sequentially followed by dolomite and kaolinite cements which continue the trend towards light isotopic values. This trend is continued with younger, fault-controlled dolomite, and is terminated by vein-filling calcite and dolomite. The younger calcite, interpreted as a near-surface precipitate from meteoric waters, is unrelated to the older sequence of carbonates and has distinctly different carbon isotope ratios: δ13C ? 6-8‰.  相似文献   

11.
贾鹏  李伟  卢远征  樊茹  李鑫  李明  曾乙洋  刘鑫 《现代地质》2016,30(6):1329-1338
摘要：四川盆地中南部地区寒武系洗象池群碳酸盐岩的碳、氧同位素组成受后期成岩作用影响较小,基本保留了原始海洋的同位素组成,根据该地区采集的88个碳、氧同位素数据,研究、讨论了中上寒武统碳酸盐岩不同尺度沉积旋回中的碳氧同位素组成、演化及地质意义。研究表明,四川盆地寒武系洗象池群由下至上的地层序列中,碳、氧同位素具有明显的旋回性演化特征：其δ13C值变化于－56‰～3247‰之间,均值为-0979‰,绝大多数的样品都在-2‰～2‰的区间震荡,δ18O值分布于-111‰～-52‰之间,均值为-6934‰,主要集中在－9‰～-6‰的范围内波动。通过对不同尺度沉积旋回碳、氧同位素数据分析研究,认为在体系域尺度沉积旋回中控制碳氧同位素组成特征的主因是海平面变化,在米级旋回中主要受高频海平面变化、古气候、古构造等多方面叠加的影响;通过对碳、氧同位素数据分析研究,首次明确了该地区芙蓉统的底界,为地层的划分对比提供了有力证据;洗象池群早期和中期经历了短暂而快速的海侵后进入缓慢的海退,在晚期缓慢海侵后的快速海退,碳同位素组成反映的海平面变化趋势与沉积相演化一致。  相似文献   

12.
Isotope geochemistry of caliche developed on basalt   总被引：1，自引：0，他引：1  
Enormous variations in oxygen and carbon isotopes occur in caliche developed on < 3 Ma basalts in 3 volcanic fields in Arizona, significantly extending the range of δ18O and δ13C observed in terrestrial caliche. Within each volcanic field, δ18O is broadly co-variant with δ13C and increases as δ13C increases. The most 18O and 13C enriched samples are for subaerial calcite developed on pinnacles, knobs, and flow lobes that protrude above tephra and soil. The most 18O and 13C depleted samples are for pedogenic carbonate developed in soil atmospheres. The pedogenic caliche has δ18O fixed by normal precipitation in local meteoric waters at ambient temperatures and has low δ13C characteristic of microbial soil CO2. Subaerial caliche has formed from 18O-rich evapoconcentrated meteoric waters that dried out on surfaces after local rains. The associated 13C enrichment is due either to removal of 12C by photosynthesizers in the evaporating drops or to kinetic isotope effects associated with evaporation. Caliche on basalt lava flows thus initially forms with the isotopic signature of evaporation and is subsequently over-layered during burial by calcite carrying the isotopic signature of the soil environment. The large change in carbon isotope composition in subsequent soil calcite defines an isotopic biosignature that should have developed in martian examples if Mars had a “warm, wet” early period and photosynthesizing microbes were present in the early soils. The approach can be similarly applied to terrestrial Precambrian paleocaliche in the search for the earliest record of life on land. Large variations reported for δ18O of carbonate in Martian meteorite ALH84001 do not necessarily require high temperatures, playa lakes, or flood runoff if the carbonate is an example of altered martian caliche.  相似文献   

13.
河东煤田晚古生代层序地层的碳氧同位素特征   总被引：3，自引：1，他引：2  
系统分析了河东煤田上石炭统(C2)-下二叠统下部(P11)45个碳酸盐岩样品的碳氧同位素在层序中的分布特征,探讨了碳氧同位素应用于层序划分及对比、相对海平面变化研究及晚古生代地层沉积相研究的可能性。研究表明,碳氧同位素在C2及P11的三级层序中的分布特征是不相同的,从TST到HST,在C2的三级层序中,δ13C及δ18O不断变重;在P11的三级层序中,δ13C不断变轻,而δ18O不断变重。这种规律在P11每个三级层序中均相似,垂向上显示出韵律性。横向上,δ13C及Z值总体具有由北向南升高的趋势。碳氧同位素在层序中的分布是受聚煤作用、陆源物质的注入、古气候、沉积环境及时间等控制的。   相似文献   

14.
云南鹤庆锰矿位于扬子地台西南缘,对其岩石样品的碳氧同位素分析表明,上三叠统松桂组经历了一次海进和一次漫长的海退期。生物(藻类)代谢与海水发生同位素交换、古气候环境的变化和古海水深度的变化都使反演的古温度偏高;古盐度分析显示正常海相沉积特征,略低的盐度与碳同位素偏低有关。钻孔样品的氧同位素主要由盐度变化而产生一个高值范围,且对应碳同位素低值区,由于海平面下降,有机质埋藏率低导致碳同位素向负值漂移。根据以上分析认为,沉积时期的环境至少是一个半局限的浅海近陆源盆地,伴随扬子地台不断抬升,气候由潮湿、炎热转变为干燥的大陆性气候,锰矿的形成也是伴随海退海水变浅而沉积成矿。  相似文献   

15.
Water temperature, oxygen isotope composition and the δ13C of dissolved inorganic carbon were measured in 2 southern Michigan rivers, the Huron River and Fleming Creek, between late September 1990 and June 1992. The final full year of shell growth in 3 unionids collected in 1992 from these rivers was sampled for stable isotope analysis with a resolution of 30 μm. The δ18O of both shell nacre and the prismatic layer is accurately predicted by a fractionation relationship developed for biogenic aragonite. High resolution sampling of 3 species and bulk sampling of 3 other species suggest that all unionids adhere to this oxygen isotope fractionation relationship. This relationship is used to show that shell growth ceases below approximately 12°C. In these 2 settings the average δ18O value of shell (PDB scale) is within 0.5‰ of the average δ18O of river water (SMOW scale). Unionids can therefore be used in oxygen-isotope-based paleoclimatic and paleohydrologic reconstructions. In contrast, the carbon isotope ratio of shell is not accurately predicted by published fractionation factors between D.I.C. and carbonate. Shell δ13C is more negative than predicted values and the offset is highly variable suggesting a significant and variable incorporation of metabolic carbon into the shell carbonate.  相似文献   

16.
Offsets from isotopic equilibrium in biogenic carbonates have complicated paleoclimate reconstructions for decades. A new archive of climate, deep-sea corals, is used to evaluate the calcification processes, independent of photosynthesis, that contribute to these offsets. Carbon and oxygen stable isotope data from six modern deep-sea corals show strong linear trends between δ13C and δ18O. Slopes of these trends between samples are similar and range between 1.9 to 2.6 for Δδ13C/Δδ18O. Linear trends intersect isotopic equilibrium for δ18O and are slightly depleted for δ13C. Variations in the isotopic ratios are strongly correlated with the density banding structure. Isotopically depleted aragonite is associated with light, quickly precipitating bands, whereas isotopically enriched points correspond to slowly accumulating, less dense aragonite. The densest white band at the trabecular center is furthest from isotopic equilibrium for both carbon and oxygen. Data from this region fall off the linear trend between δ18O and δ13C. This deviation, where δ13C remains constant while the δ18O continues to decrease, does not support “vital effect” mechanisms that call upon kinetic fractionation to explain offsets from isotopic equilibrium. We propose a new mechanism for vital effects in these deep-sea corals that is based on a thermodynamic response to a biologically induced pH gradient in the calcifying region.  相似文献   

17.
Peter K. Swart 《Sedimentology》2015,62(5):1233-1304
Stable carbon and oxygen isotopes (δ18O and δ13C values) and trace elements have been applied to the study of diagenesis of carbonate rocks for over 50 years. As valuable as these insights have been, many problems regarding the interpretation of geochemical signals within mature rocks remain. For example, while the δ18O values of carbonate rocks are dependent both upon the temperature and the δ18O value of the fluid, and additional information including trace element composition aids in interpreting such signals, direct evidence of either the temperature or the composition of the fluids is required. Such information can be obtained by analysing the δ18O value of any fluid inclusions or by measuring the temperature using a method such as the ‘clumped’ isotope technique. Such data speak directly to a large number of problems in interpreting the oxygen isotope record including the well‐known tendency for δ18O values of carbonate rocks to decrease with increasing age. Unlike the δ18O, δ13C values of carbonates are considered to be less influenced by diagenesis and more a reflection of primary changes in the global carbon cycle through time. However, many studies have not sufficiently emphasized the effects of diagenesis and other post‐depositional influences on the eventual carbon isotopic composition of the rock with the classic paradigm that the present is the key to the past being frequently ignored. Finally, many additional proxies are poised to contribute to the interpretation of carbonate diagenesis. Although the study of carbonate diagenesis is at an exciting point with an explosion of new proxies and methods, care should be taken to understand both old and new proxies before applying them to the ancient record.  相似文献   

18.
The oxygen isotopic composition of land-snail shells may provide insight into the source region and trajectory of precipitation. Last glacial maximum (LGM) gastropod shells were sampled from loess from Belgium to Serbia and modern land-snail shells both record δ18O values between 0‰ and − 5‰. There are significant differences in mean fossil shell δ18O between sites but not among genera at a single location. Therefore, we group δ18O values from different genera together to map the spatial distribution of δ18O in shell carbonate. Shell δ18O values reflect the spatial variation in the isotopic composition of precipitation and incorporate the snails' preferential sampling of precipitation during the warm season. Modern shell δ18O decreases in Europe along a N-S gradient from the North Sea inland toward the Alps. Modern observed data of isotopes in precipitation (GNIP) demonstrate a similar trend for low-altitude sites. LGM shell δ18O data show a different gradient with δ18O declining toward the ENE, implying a mid-Atlantic source due to increased sea ice and a possible southern displacement of the westerly jet stream. Balkan LGM samples show the influence of a Mediterranean source, with δ18O values decreasing northward.  相似文献   

19.
张云峰  王清晨 《地质科学》2007,42(3):570-578
对济阳坳陷奥陶系碳酸盐原岩及孔洞缝中充填方解石进行了C、O同位素测定,结果表明孔洞缝充填方解石的δ13C和δ18O值比原岩偏负。奥陶系三山子组和马家沟组孔缝中充填的方解石C、O同位素演化有很大区别,前者的δ13C和δ18O值均为负值,δ13C向较高负值偏移,δ18O值向较低负值偏移;马家沟组八陡段孔缝充填方解石的δ13C和δ18O值也多为负值,δ13C向较正值方向偏移,δ18O值向较高负值偏移。奥陶系碳酸盐岩孔缝充填方解石形成于大气淡水环境和埋藏成岩环境,次生孔洞可能主要形成于早期表生阶段,裂缝形成于中-新生代的构造运动,方解石主要充填于埋藏环境中。次生孔缝的主要形成时期早于油气大量运移期,对古潜山油藏的形成有利。  相似文献   

20.
Nineteen samples of metamorphosed carbonate-bearing rocks were analyzed for carbon and oxygen isotope ratios by ion microprobe with a ∼5-15 μm spot, three from a regional terrain and 16 from five different contact aureoles. Contact metamorphic rocks further represent four groups: calc-silicate marble and hornfels (6), brucite marble (2), samples that contain a reaction front (4), and samples with a pervasive distribution of reactants and products of a decarbonation reaction (4). The average spot-to-spot reproducibility of standard calcite analyses is ±0.37‰ (2 standard deviations, SD) for δ18O and ±0.71‰ for δ13C. Ten or more measurements of a mineral in a sample that has uniform isotope composition within error of measurement can routinely return a weighted mean with a 95% confidence interval of 0.09-0.16‰ for δ18O and 0.10-0.29‰ for δ13C. Using a difference of >6SD as the criterion, only four of 19 analyzed samples exhibit significant intracrystalline and/or intercrystalline inhomogeneity in δ13C at the 100-500 μm scale, with differences within individual grains up to 3.7‰. Measurements are consistent with carbon isotope exchange equilibrium between calcite and dolomite in five of six analyzed samples at the same scale. Because of relatively slow carbon isotope diffusion in calcite and dolomite, differences in δ13C can survive intracrystalline homogenization by diffusion during cooling after peak metamorphism and likely represent the effects of prograde decarbonation and infiltration. All but 2 of 11 analyzed samples exhibit intracrystalline differences in δ18O (up to 9.4‰), intercrystalline inhomogeneity in δ18O (up to 12.5‰), and/or disequilibrium oxygen isotope fractionations among calcite-dolomite, calcite-quartz, and calcite-forsterite pairs at the 100-500 μm scale. Inhomogeneities in δ18O and δ13C are poorly correlated with only a single mineral (dolomite) in a single sample exhibiting both. Because of relatively rapid oxygen isotope diffusion in calcite, intracrystalline inhomogeneities in δ18O likely represent partial equilibration between calcite and fluid during retrograde metamorphism. Calcite is in oxygen isotope exchange equilibrium with forsterite in one of four analyzed samples, in equilibrium with dolomite in none of six analyzed samples, and in equilibrium with quartz in neither of two analyzed samples. There are no samples of contact metamorphic rock with analyzed reactants and products of an arrested metamorphic reaction that are in oxygen isotope equilibrium with each other. The degree of departure from equilibrium in analyzed samples is variable and is often related, at least in part, to alteration of δ18O of calcite during retrograde fluid-rock reaction. In situ sub-grain-scale carbon and oxygen isotope analyses of minerals are advisable in the common applications of stable isotope geochemistry to metamorphic petrology. Correlation of sub-mm scale stable isotope data with imaging will lead to improved understanding of reaction kinetics, reactive fluid flow, and thermal histories during metamorphism.  相似文献   

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