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1.
This work reports a study on the rare-earth element (REE) behaviour in the high-sulfidation-type superficial alteration and in the phyllic and propylitic alteration in the subsurface of the island of Vulcano. The results of this study demonstrate notable differences in the REE behaviour in the different alteration facies. In silicic alteration, all REE are equally strongly depleted; in advanced argillic alteration, LREE are quite immobile whereas HREE are strongly depleted; in intermediate argillic, phyllic and propylitic alteration, REE patterns are almost unchanged compared with their fresh rock equivalents. These features indicate that the behaviour of REE in hydrothermal alteration facies at La Fossa is mainly controlled by pH, availability of complexing ions in the fluid (mainly SO42− and, in the silicic facies, F−) and the presence of secondary minerals able to host REE in their structures. The origin of the acid fluids is related to the hypogenic introduction of prevalently magmatic acid gases produced by the degassing of the shallow magmatic system of La Fossa volcano. In the active high-temperature fumarolic field of La Fossa, REE behaviour illustrates the transition from a dry vapor system, corresponding to the high-temperature fumaroles, to a wet condensing system in the surrounding area. The results of this research, carried out on an active high-sulfidation system, provide a useful tool for the study of high-sulfidation epithermal ore deposits and particularly help to understand the alteration processes during the main stage of hypogene wall rock alteration.  相似文献   

2.
High-sulfidation (HS) epithermal systems have elements in common with passively degassing volcanoes associated with high T, acid fumarole fields or acid crater lakes. They are considered to form in two stages, the first of which involves advanced argillic alteration resulting from intense, strongly acidic fluid–rock interaction. The La Fossa hydrothermal system (Vulcano Island) represents a classic example of such an active HS system and can be considered as a modern analogue of this early stage of alteration, resulting in a core of intense silicic (90–95% pure SiO2) alteration surrounded by alunitic alteration zones.  相似文献   

3.
北武夷梨子坑火山盆地流纹斑岩与铅锌矿的成因关系   总被引：1，自引：0，他引：1  
摘要：梨子坑火山盆地位于北武夷中生代月凤山-梨子坑火山岩带东段,已知铅锌（铜、银）矿体或矿化呈细脉-浸染型、脉状,产于流纹斑岩脉的内外接触带及其外侧围岩中,发育钾化、绿泥石化、硅化、绿帘石化等围岩蚀变。地球化学特征显示流纹斑岩为钙碱性系列,岩石具有高SiO2、富碱、高K2O、高钙铁、低镁、K2O／Na2O值偏高的特点,为强过铝质岩石。w（∑REE）值为76．28×10^-6～222．54×10＆-6（∑LREE／∑HREE）比值较大,为4．08-12．30,属于轻稀土元素富集型。成矿流纹斑岩形成于1372=2．1Ma（SHRIMP锆石U—Pb法）～138．8±1．4Ma（LA-MC—ICPMS锆石U—Pb法）,属早白垩世。铅锌矿属于次火山斑岩脉型铅锌（银铜）成矿系列,划分为次火山斑岩脉型和次火山热液破碎带型两种矿床成因类型。  相似文献   

4.
Extensive lava flows were erupted during the Upper Cretaceous in the Wadi Natash of southern Egypt. The lavas are mainly of alkaline (sodium dominated) composition and include alkali olivine basalt (AOB), hawaiite, mugearite, and benmoreite that intruded with acidic volcanics of trachytic to rhyolitic composition. Abundances of major oxides and trace elements including the REE vary systematically through this compositional spectrum. The gradual decrease of CaO with decreasing MgO is consistent with the dominance of phenocrysts of labradoritic plagioclase (An75–62) and Mg-rich olivine (Fo84–80) in the AOB and hawaiite. Olivine phenocrysts are normally zoned with cores consistent with crystallization from a magma having the bulk-rock composition. The sharp decrease of alkalis at low MgO contents (∼0.4% MgO) indicates significant alkali feldspar fractionation during the evolution of trachytes and rhyolites. All Natash lavas show steep chondrite-normalized REE patterns with considerable LREE/HREE fractionation and a regular decrease in La/Lu ratios from the least to the most evolved lavas (La/Lun=12.5−9.5). The low absolute abundances of HREE in basic members reflects residual garnet in the source. The basic lavas have experienced compositional modifications after they segregated from the source as evidenced by lower averages of Mg# (51), Ni (134) and Cr (229) in the AOB. Much of this variation can be explained by variable degrees of polybaric fractional crystallization. Petrographic and geochemical data supported by quantitative modelling suggest the evolution of the Natash Lavas from a common AOB parent in multiple, short-lived magma chambers. In agreement with the phenocryst mineralogy of the Natash lavas, the geochemical models suggest that with increasing degree of differentiation, Mg-rich olivine, calcic plagioclase, and augite are joined and progressively substituted by ferrohedenbergite, alkali feldspars and magnetite. The OIB (ocean island basalt)-like nature of the AOB and hawaiite lavas suggests that the volumetrically dominant source component is the asthenospheric mantle. A mantle-plume source is suggested for the Natash basaltic lavas, with the lavas being generated by partial melting of a garnet peridotite in the asthenosphere.  相似文献   

5.
The lower Yangtze River area, situated at the fore-land of the Qinling-Dabie orogen, is an important re-gion for high-grade mineral deposits in Cen-tral-Eastern China. Nearly 300 different types of Cu and Au polymetal, Fe, and S mineral deposits have been found and mined in this zone[1,2]. The overall distribution of these deposits follows the trend of the Mesozoic igneous rocks, suggesting their fundamental controls on the formation of these deposits. Geo-physical and geologic observatio…  相似文献   

6.
Fumarolic encrustations and natrocarbonatite lava from the active crater of Oldoinyo Lengai volcano, Tanzania, were sampled and analysed. Two types of encrustation were distinguished on the basis of their REE content, enriched (~ 2800–5600 × [REEchondrite]) and depleted (~ 100–200 × [REEchondrite]) relative to natrocarbonatite (1700–1900 × [REEchondrite]. REE-enriched encrustations line the walls of actively degassing fumaroles, whereas REE-depleted encrustations occur mainly along cracks in and as crusts on cooling natrocarbonatite lava flows; one of the low REE encrustation samples was a stalactite from the wall of a possible fumarole. The encrustations are interpreted to have different origins, the former precipitating from volcanic gas and the latter from meteoric/ground water converted to steam by the heat of the overlying lava flow(s). REE-profiles of encrustations and natrocarbonatite are parallel, suggesting that there was no preferential mobilization of specific REE by either volcanic vapour or meteoric water vapour. The elevated REE-content of the first group of encrustations suggests that direct REE-transport from natrocarbonatite to volcanic vapour is possible. The REE trends observed in samples precipitating directly from the volcanic vapour cannot be explained by dry volatility based on the available data as there is no evidence in the encrustation compositions of the greatly enhanced volatility predicted for Yb and Eu. The observed extreme REE-fractionation with steep La/Sm slopes parallel to those of the natrocarbonatite reflects solvation and complexation reactions in the vapour phase that did not discriminate amongst the different REE or similar transport of REE in both the natrocarbonatite magma and its exsolving vapour. The low concentrations of REE in the encrustations produced by meteoric vapour suggest that the temperature was too low or that this vapour did not contain the ligands necessary to permit significant mobilization of the REE.  相似文献   

7.
High-precision Nb, Ta, Zr, Hf, Sm, Nd and Lu concentration data of depleted mantle rocks from the Balmuccia peridotite complex (Ivrea Zone, Italian Alps) were determined by isotope dilution using multiple collector inductively coupled plasma mass spectrometry (MC-ICPMS) and thermal ionisation mass spectrometry (TIMS). The Zr/Hf ratios of all investigated samples from the Balmuccia peridotite complex are significantly lower than the chondritic value of 34.2, and the most depleted samples have Zr/Hf ratios as low as 10. Correlated Zr/Hf ratios and Zr abundances of the lherzolites preserve the trend of a mantle residue that has been depleted by fractional melting. This trend confirms experimental studies that predict Hf to behave more compatibly than Zr during mantle melting. Experimentally determined partition coefficients imply that the major Zr and Hf depletion most likely occurred in the spinel stability field, with (DZr/DHf)cpx≈0.5, and not in the garnet stability field, where (DZr/DHf)grt is probably close to one. However, minor amounts of melting must have also occurred in a garnet facies mantle, as indicated by low Sm/Lu ratios in the Balmuccia peridotites. The Nb/Ta ratios of most lherzolites are subchondritic and vary only from 7 to 10, with the exception of three samples that have higher Nb/Ta ratios (18–24). The overall low Nb/Ta ratios of most depleted mantle rocks confirm a higher compatibility of Ta in the mantle. The uniform Nb/Ta ratios in most samples imply that even in ‘depleted’ mantle domains the budget of the highly incompatible Nb and Ta is controlled by enrichment processes. Such a model is supported by the positive correlation of Zr/Nb with the Zr concentration. However, the overall enrichment was weak and did barely affect the moderately incompatible elements Zr and Hf. The new constraints from the partitioning behaviour of Zr–Hf and Nb–Ta provide important insights into processes that formed the Earth’s major silicate reservoirs. The correlation of Zr/Hf and Sm/Nd in depleted MORB can be assigned to previous melting events in the MORB source. However, such trends were unlikely produced during continental crust formation processes, where Sm/Nd and Zr/Hf are decoupled. The different fractionation behaviour of Zr/Hf and Sm/Nd in the depleted mantle (correlated) and the crust (decoupled) indicates that crustal growth by a simple partial melting process in the mantle has little effect on the mass budget of LREE and HFSE between crust and mantle. A more complex source composition, similar to that of modern subduction rocks, is needed to fractionate the LREE, but not Zr/Hf and the HREE.  相似文献   

8.
Marine limestones from southern Germany were analysed by the non-destructive neutron activation/Ge(Li) spectrometric method for La, Ce, Sm, Eu, Tb, Yb, Lu, Sr, Ta, U, Sc, Th, Cr, Hf, Cs, Fe and Rb. On the basis of carbonate and non-carbonate portions of the rock, the elements could be divided into (1) those associated with clastic material (Sc, Cr, Hf, etc.), (2) those which were partly associated with authigenic material (REE), and (3) those with pronounced diagenetic history (Sr, U). The calculated effective REE distribution coefficient (Di,eff) between CaCO3 and seawater varied from about 1400 for La to about 460 for Lu suggesting fractionation of the lighter and the heavier REE's in favour of the former.  相似文献   

9.
The Middle-Late Jurassic Cu-Pb-Zn-bearing and W-bearing granites in the Nanling Range have distinctly different mineralogical and geochemical signatures. The Cu-Pb-Zn-bearing granites are dominated by metaluminous amphibole-bearing granodiorites, which have higher CaO/(Na2O+K2O) ratios, light/heavy rare earth element(LREE/HREE) ratios, and δEu values,lower Rb/Sr ratios, and weak Ba, Sr, P, and Ti depletions, exhibiting low degrees of fractionation. The W-bearing granites are highly differentiated and peraluminous, and they have lower CaO/(Na2O+K2O) ratios, LREE/HREE ratios, and δEu values,higher Rb/Sr ratios, and strong Ba, Sr, P, and Ti depletions. The Cu-Pb-Zn-bearing granites were formed predominantly between155.2 and 167.0 Ma with a peak value of 160.6 Ma, whereas the W-bearing granites were formed mainly from 151.1 to 161.8Ma with a peak value of 155.5 Ma. There is a time gap of about 5 Ma between the two different types of ore-bearing granites.Based on detailed geochronological and geochemical studies of both the Tongshanling Cu-Pb-Zn-bearing and Weijia W-bearing granites in southern Hunan Province and combined with the other Middle-Late Jurassic Cu-Pb-Zn-bearing and W-bearing granites in the Nanling Range, a genetic model of the two different types of ore-bearing granites has been proposed. Asthenosphere upwelling and basaltic magma underplating were induced by the subduction of the palaeo-Pacific plate. The underplated basaltic magmas provided heat to cause a partial melting of the mafic amphibolitic basement in the lower crust, resulting in the formation of Cu-Pb-Zn mineralization related granodioritic magmas. With the development of basaltic magma underplating,the muscovite-rich metasedimentary basement in the upper-middle crust was partially melted to generate W-bearing granitic magmas. The compositional difference of granite sources accounted for the metallogenic specialization, and the non-simultaneous partial melting of one source followed by the other brought about a time gap of about 5 Ma between the Cu-Pb-Zn-bearing and W-bearing granites.  相似文献   

10.
Zilong  Li  Yoshiaki  Tainosho  Jun-Ichi  Kimura  Kazuyuki  Shiraishi 《Island Arc》2005,14(4):636-652
Abstract The Mefjell plutonic complex consists of 500–550‐Ma Pan‐African plutonic rocks, which intrude into the Precambrian crystalline basement in the Sør Rondane Mountains, East Antarctica, and forms part of the Sør Rondane Suture Zone. The complex comprises syenitic and granitic (mostly monzogranitic) rocks, and is characterized by the presence of iron‐rich hydrous mafic minerals and primary ilmenite, both of which imply its formation at high temperature and under low oxygen fugacity conditions. The syenitic rocks are metaluminous, and are high in alkalis, K2O/Na2O, Al2O3, FeOt/(FeOt + MgO) (0.88–0.98), K/Rb (800–1000), Ga (18–28 p.p.m.), Zr (up to 2100 p.p.m.) and Ba. They also have a low Mg? (Mg/[Mg + Fe2+]), Rb, Sr, Nb, Y and F, low to moderate light rare earth element (LREE)/heavy rare earth element (HREE) ratios and positive Eu anomalies in their rare earth element (REE) patterns. The granitic rocks are metaluminous to peraluminous, and have a high Rb content, high Sr/Ba and LREE/HREE ratios, low K/Rb and negative Eu anomalies. Most of the syenitic and granitic rocks have Y/Nb ratios greater than 1.2, and are depleted in Nb, Ti and Sr on the primitive mantle‐normalized spider diagrams, indicating a crustal origin with subduction zone signatures. We interpret both the syenitic and granitic rocks to be derived from an iron‐rich lower crustal source by dehydration melting induced by the heat of mantle‐derived basaltic intrusion, after which they then underwent limited fractional crystallization. The Mefjell plutonic complex has a high Zr content and tectonic discrimination diagram signatures indicative of normal A‐type granitic rocks. Both rock suites may have been generated under the same postorogenic tectonic setting. The Mefjell syenitic rocks are chemically comparable to charnockites in the Gjelsvikjella and western Mühlig‐Hofmannfjella areas of East Antarctica, whereas the granitic rocks are comparable to aluminous A‐type granitic rocks in South India, which were emplaced during formation and evolution of the Gondwanaland supercontinent.  相似文献   

11.
Field observation showed that there are many irregular leucocratic intrusive rocks in pillow lavas in the Danfeng Group in the Xiaowangjian area, north Qinling orogenic belt. Photomicrographs indicated that the protoliths of those altered leucocratic intrusive rocks are dioritic rocks. Geochemical analyses showed that pillow lavas have a range of SiO2 from 47.35% to 51.20%, low abundance of TiO2 from 0.97% to 1.72%, and percentages of MgO (MgO#=41―49). Chondrite-normalized REE patterns of pillow lavas are even, indicative of a weak differentiation between LREE and HREE (La/YbN=1.52―0.99). N-MORB-normalized trace element abundances showed that pillow lavas are enriched in incompatible elements (e.g., K, Rb, and Ba). Leucocratic intrusive rocks in pillow lavas have a wide range of SiO2 from 53.85%―67.20%, low abundances of TiO2 from 0.51%―1.10%, and MgO (MgO#=40―51), and higher percentages of Al2O3 (13.32%―16.62%) and concentration of Sr (342-539 μg/g), ratios of Na2O/K2O (2―7) and Sr/Y (17―28). Chondrite-normalized REE patterns of leucocratic intrusive rocks showed highly differentiation between LREE and HREE (La/YbN=12.26―19.41). N-MORB-normalized trace element abundances showed that leucocratic intrusive rocks are enriched in incompatible elements (e.g., K, Rb, and Ba), and significantly depleted in HFSE (e.g., Nb, Ta, Zr and Ti), indicative of a relationship to subduction. Isotopically, leucocratic intrusive rocks have a similar εNd(t) ( 7.45― 13.14) to that of MORB ( 8.8― 9.7), which indicates that those leucocratic intrusive rocks sourced from depleted mantle most likely. SHRIMP U-Pb analyses for zircon showed that those leucocratic intrusive rocks were formed at 442±7 Ma, yielding an age of subduction in the early Paleozoic in the north Qinling orogenic belt.  相似文献   

12.
A combination of field mapping, geochemistry, and remote sensing methods has been employed to determine the extent of hydrothermal alteration and assess the potential for failure at the Santiaguito lava dome complex, Guatemala. The 90-year-old complex of four lava domes has only experienced relatively small and infrequent dome collapses in the past, which were associated with lava extrusion. However, existing evidence of an active hydrothermal system coupled with intense seasonal precipitation also presents ideal conditions for instability related to weakened clay-rich edifice rocks. Mapping of the Santiaguito dome complex identified structural features related to dome growth dynamics, potential areas of weakness related to erosion, and locations of fumarole fields. X-ray diffraction and backscattered electron images taken with scanning electron microscopy of dacite and ash samples collected from around fumaroles revealed only minor clay films, and little evidence of alteration. Mineral mapping using ASTER and Hyperion satellite images, however, suggest low-temperature (<150 °C) silicic alteration on erosional surfaces of the domes, but not the type of pervasive acid-sulfate alteration implicated in collapses of other altered edifices. To evaluate the possibility of internal alteration, we re-examined existing aqueous geochemical data from dome-fed hot springs. The data indicate significant water–rock interaction, but the Na–Mg–K geoindicator suggests only a short water residence time, and δ18O/δD ratios show only minor shifts from the meteoric water line with little precipitation of secondary (alteration) minerals. Based on available data, hydrothermal alteration on the dome complex appears to be restricted to surficial deposits of hydrous silica, but the study has highlighted, importantly, that the 1902 eruption crater headwall of Santa María does show more advanced argillic alteration. We also cannot rule out the possibility of advanced alteration within the dome complex interior that is not accessible to the methods used here. It may therefore be prudent to employ geophysical methods to make further assessments in the future.  相似文献   

13.
Chlorine- and sulphur-bearing compounds in fumarole discharges of the La Fossa crater at Vulcano Island (Italy) can be modelled by a mixing process between magmatic gases and vapour from a boiling hydrothermal system. This allows estimating the compounds in both endmembers. Magma degassing cannot explain the time variation of sulphur and HCl concentrations in the deep endmember, which are more probably linked to reactions of solid phases at depth, before mixing with the hydrothermal vapours. Based on the P–T conditions and speciation of the boiling hydrothermal system below La Fossa, the HCl and Stot contents in the hydrothermal vapours were used to compute the redox conditions and pH of the aqueous solution. The results suggest that the haematite–magnetite buffer controls the hydrothermal fO2 values, while the pH has increased since the end of the 1970s. The main processes affecting pH values may be linked to Na–Ca exchanges between evolved seawater, feeding the boiling hydrothermal system, and local rocks. While Na is removed from water, calcium enters the solution, undergoes hydrolysis and produces HCl, lowering the pH of the water. The increasing water–rock ratio within the hydrothermal system lowers the Ca availability, so the aqueous solution becomes less acidic. Seawater flowing towards the boiling hydrothermal brine dissolves a large quantity of pyrite along its path. In the boiling hydrothermal system, dissolved sulphur precipitates as pyrite and anhydrite, and becomes partitioned in vapour phase as H2S and SO2. These results are in agreement with the paragenesis of hydrothermal alteration minerals recovered in drilled wells at Vulcano and are also in agreement with the isotopic composition of sulphur emitted by the crater fumaroles.  相似文献   

14.
Hydrothermal systems in regions of high relief may not have obvious thermal features indicative of their central upflow zone at depth. Investigation of such areas for geothermal energy production in the Philippines has, however, encountered relatively large ( > 10,000 m2) areas of volumetrically significant but diffuse, cold-gas emission and associated intense argillic alteration. These features are likely to be best developed above, or close to, hydrothermal upflow zones. The identification of such features is important for interpreting the hydrology of active geothermal systems in the course of exploration for power development, or when interpreting the paleohydrology of fossil geothermal systems which host epithermal mineral deposits. Such zones of argillic alteration are likely to be barren of precious metals or other elements (except mercury) which are commonly used as pathfinders for precious-metal deposits, but are indicative of subsurface processes significant in ore genesis.It is proposed that the term “kaipohan” be used for such features. Their existence depends on the presence of either a low-permeability geologic formation or where a suitable relationship exists between the hydrology of the deep geothermal reservoir and that of the shallow groundwater system. Such a situation occurs in steep terrain, where much of the area supplying meteoric recharge to the geothermal system is at a lower elevation than the area overlying the centre of the system, and where there is a high annual rainfall. These conditions are typical of andesitic stratovolcanoes in tropical or subtropical island arcs.  相似文献   

15.
The chemical composition and D/H, and ratios have been determined for the acid hot waters and volcanic gases discharging from Zaō volcano in Japan. The thermal springs in Zaō volcano issue acid sulfate-chloride type waters (Zaō) and acid sulfate type waters (Kamoshika). Gases emitted at Kamoshika fumaroles are rich in CO2, SO2 and N2, exclusive of H2O. Chloride concentrations and oxygen isotope data indicate that the Zaō thermal waters issue a fluid mixture from an acid thermal reservoir and meteoric waters from shallow aquifers. The waters in the Zaō volcanic system have slight isotopic shifts from the respective local meteoric values. The isotopic evidence indicates that most of the water in the system is meteoric in origin. Sulfates in Zaō acid sulfate-chloride waters with δ34S values of around +15‰, are enriched in 34S compared to Zaō H2S, while the acid sulfate waters at Kamoshika contain supergene light sulfate (δ34S = + 4‰) derived from volcanic sulfur dioxide from the volcanic exhalations. The sulfur species in Zaō acid waters are lighter in δ34S than those of other volcanic areas, reflecting the difference in total pressure.  相似文献   

16.
Clay fractions in the non-calcareous surface sediments from the eastern Pacific were analyzed for clay minerals, REE and 143Nd/144Nd. Montmorillonite/illite ratio (M/I ratio), total REE contents (ΣREE), LREE/HREE ratio and cerium anomaly (δCe) may effectively indicate the genesis of clay minerals. Clay fractions with M/I ratio <1, δCe >0.85, ΣREE <400 μg/g, LREE/HREE ratio ≈4, and REE patterns similar to those of pelagic sediments are terrigenous and autogenetic mixed clay fractions and contain more autogenetic montmorillonite. Clay fractions with M/I ratio >1, δCe=0.86 to 1.5, ΣREE=200 to 350 μg/g, LREE/HREE ratio ≈6 and REE distribution patterns similar to that of China loess are identified as terrigenous clay fraction. The 143Nd/144Nd ratios or ɛNd values of clay fractions inherit the features of terrigenous sources of clay minerals. Clay fractions are divided into 4 types according to ɛNd values. Terrigenous clay minerals of type I with the ɛNd values of ™8 to ™6 originate mainly from North American fluvial deposits. Those of type II with the ε Nd values of ™9 to ™7 are mainly from the East Asia and North American fluvial deposits. Those of type III with ε Nd values of ™6 to ™3 could come from the central and eastern Pacific volcanic islands. Those of type IV with ε Nd values of ™13 to ™12 may be from East Asia eolian. The terrigenous and autogenetic mixed clay fractions show patchy distributions, indicating that there are volcanic or hot-spot activities in the eastern Pacific plate, while the terrigenous clay fractions cover a large part of the study area, proving that the terrigenous clay minerals are dominant in the eastern Pacific.  相似文献   

17.
Papandayan is a stratovolcano situated in West Java, Indonesia. Since the last magmatic eruption in 1772, only few hydrothermal explosions have occurred. An explosive eruption occurred in November 2002 and ejected ash and altered rocks. The altered rocks show that an advanced argillic alteration took place in the hydrothermal system by interaction between acid fluids and rocks. Four zones of alteration have been defined and are limited in extension and shape along faults or across permeable structures at different levels beneath the active crater of the volcano.  相似文献   

18.
Petrographic analysis and chemical analysis of major and trace elements including rare earth elements of the Neoproterozoic sandstones from the Chandarpur Group and the Tiratgarh Formation have been carried out to determine their provenance, tectonic setting and weathering conditions. All sandstone samples are highly enriched in quartz but very poor in feldspar and lithic fragments. Petrographically and geochemically these sandstones are classified as subarkose, sublitharenite and arenite. The Chemical Index of Alteration (CIA mean 68) and Th/U ratios (mean 4.2) for these sandstones suggest their moderate weathering nature. Generally, all sandstone samples are strongly depleted in major elements (except SiO2), trace elements (except Zr) and REE in comparison with Post Archean Australian Shale (PAAS) and Upper Continental Crust (UCC). Their mineralogy and mean of elemental ratios suitable for determination of provenance and tectonic setting, e.g. Al2O3/SiO2 (0.02), K2O/Na2O (10), Eu/Eu* (0.67), (La/Lu)n (10.4), La/Sc (3), Th/Sc (1.2), La/Co (0.22), Th/Co (0.08), and Cr/Th (7.2), support a felsic source and a passive margin tectonic setting for these sandstones. Also these key elemental ratios do not show much variation over a range of SiO2. Thus we attest their significance in determining source rock characteristics of quartz rich sandstones. Chondrite‐normalized REE patterns with LREE enrichment and a strong negative Eu anomaly are also attributed to felsic source rock characteristics for these sandstones. The source rocks identified are granite and gneiss of the Bastar craton. Minor amounts may have been derived from older supracrustals of the Bastar craton. However, the major element data of the Paleoproterozoic Sakoli schists when compared with those of the Neoproterozoic sandstones indicate that the schists were derived from a mafic source and deposited in an active continental margin tectonic setting. There is, however, little difference in CIA values between the Paleoproterozoic Sakoli schists and Neoproterozoic sandstones, indicating prevailing of similar (moderate‐intense) weathering conditions throughout the Proterozoic in the Bastar craton. Our study also suggests a change in the provenance and tectonic setting of deposition of sediments from dominantly a mafic source and an active continental margin in the Paleoproterozoic to dominantly granite and gneiss (felsic source) and a passive continental margin in the Neoproterozoic in the Bastar craton.  相似文献   

19.
Evidence for a deuteric alteration process induced by a magmatic fluid has been found in the feeder zone of the Mururoa volcano (French Polynesia). Within the dikes, where basaltic glass does not show any evidence of pervasive alteration, vesicles are filled with dioctahedral smectites and calcite, while olivine phenocrysts are replaced by dioctahedral smectites, ankerite and calcite.The 13C signature of carbonates, the carbon and H2O content of the whole rocks and their impoverishment in deuterium are compatible with the presence of magmatic CO2 during the crystallization of intruding lavas and exclude contamination by seawater. Mass balance calculations on selected thin sections photographs of partly filled up vesicles and replaced olivine crystals, constrain, assuming a closed system interaction, the chemical composition of the initial fluid and the respective amounts of the initial solid phases involved in the alteration process. Thermodynamic modelings using the EQ3/6 software package correctly predict the mineralogic, chemical and isotopic exchanges accompanying alteration, thus validating the closed system assumption. The model which allows prediction of the influence of CO2 on the alteration products, shows that, above a 0.25 CO2 mole fraction in the initial fluid, the alteration is entirely controlled by the chemical composition of the initial solid phases. The presence of CO2 implies the precipitation of dioctahedral smectites and carbonates instead of the magnesian smectites commonly observed in CO2-free systems.The Mururoa feeder zone shows alteration features typical of a closed system interaction between the basaltic rock and a magmatic fluid in which seawater did not take part.  相似文献   

20.
Masahiko  Yagi 《Island Arc》1993,2(4):240-261
Abstract Alteration of reservoir rocks in the Yurihara Oil and Gas Field, hereafter referred to as the ‘Yurihara field’, have been examined by using samples from six wells. These rocks are basalts in the lowermost part of the basin-fills (‘green tuff’ Formation). These basalts were produced in many eruptions in a submarine environment during the early to middle Miocene, and they underwent continuous intensive alteration genetically associated with Miocene submarine volcanism. The alteration of the basalts is of two types: low grade metamorphism and hydrothermal. The former belongs to the type of ocean floor metamorphism and comprises two subgroups: zeolite (zone I) and prehnite-pumpellyite (zones IIa: vein and amygdule occurrence, and IIb: replacing plagioclase). The latter is characterized by potassic metasomatism accompanied by adularia, quartz and calcite veins (zones IIIa: center and IIIb: margin of the metasomatism). This overprints the low grade metamorphic alteration. The central zone of hydrothermal alteration coincides with a major estimated fault, so that fluids probably assent along the fault. The basalts erupted during 16.5-15.5 Ma, determined by planktonic foraminifera assemblages of inter-bedded shales, then underwent successive low grade metamorphism. In time, the hydrothermal alteration that overprints low grade metamorphism occurred. Adularia veins of the altered rocks located in the hydrothermal alteration zones (zone IIIa and IIIb) have been dated as 9 Ma determined by the K-Ar method. This fact indicates that the activity of low grade metamorphism had already crossed the peak before hydrothermal alteration occurred at 9 Ma. The shape of isotherms of fluid inclusion homogenization temperatures (Th) and that of isolines of apparent salinity (Tm) almost coincide with each other, and these also coincide with the distribution of hydrothermal alteration (zones IIIa and IIIb). This indicates that the fluid inclusions formed at the same time as ascending fluids produced the potassic metasomatism. The maximum Th of the fluid inclusions is 222°C and Tm indicates trapped fluids of up to 3.3 wt% equivalent NaCl (i.e. almost the same as seawater). A Th versus Tm plot indicates mixing occurred between hydrothermal fluids and formation water that has low salinity. Corrensite and chlorite form veins, and the temperatures of their formation, estimated by the extent of aluminium substitution into the tetrahedral site of chlorite, ranges between 165 and 245°C in the centre of the hydrothermal alteration zone (zone IIIa). This is consistent with the result of Th analyses. The deposition temperature of chlorite associated with prehnite in veins ranges between 190 and 215°C in zones IIa and IIb.  相似文献   

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