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1.
Sulfur isotope ratios were measured in eight lava incrustations and three volcanic gas samples and their corresponding lava flows. The lava incrustations of sulfate composition are from five recent eruptions and occur as thenardite or as aphtitalite-thenardite mixtures, with abundant trace elements. The incrustations show small sulfur isotope fractionation of 1–2‰ compared with corresponding lavas and the volcanic gas samples. The sulfate incrustations are formed through oxidation of SO2 from the emitted volcanic gas and subsequent reaction with metal halides. The volcanic gas samples show a distribution of decreasing δ34S through time from +3.4 to −1.8‰; sulfate was preferentially degassed compared to sulfide. The data indicate that sulfate incrustations serve as a late-stage volcanic gas sample with respect to sulfur isotopes.  相似文献   

2.
The Cl, F, SO2 contents and Cl/F and Cl/SO4 ratios in Central American volcanic gases are examined. 103?105 tons SO2 per day are given off during eruptions and 102 when a prominent vapor cloud persists between eruptive periods. Data regarding Cl and F and SO4 from leachates, condensates, and incrustations are compared. Our data suggest circumpacific volcanoes are SO2 poor relative to Cl and may be F poor although F is higher in basaltic Central American volcanoes than others.  相似文献   

3.
The distribution of the elements F, Cl, Br and I was analysed in layers removed stepwise from Antarctic H5 and H6 chondrites. All meteorites show higher concentrations of these elements on their surfaces than in their interiors. The degree of halogen enrichment cannot be correlated with the degree of visual weathering and is proportional to the time the meteorites were residing on the surface of the Antarctic ice. During this period, aerosols, salts and gaseous components are deposited on the surfaces of the meteorites and diffuse into their interior. The observed contamination level of the meteorites is influenced by leaching properties and diffusion behaviour of the individual halogens. The major contamination source for F, Cl and probably Br is air-borne seaspray; for I it is the gaseous compound methyl iodide (CH3I) produced by biological processes in the sea. Methyl iodide and its oxidation products formed in the Antarctic atmosphere (e.g., I2) can be transported over longer distances to the interior of Antarctica than air-borne seaspray. Therefore, the ratio of the halogen contamination is related to the collection site of the meteorites. All meteorites that were found in the Antarctic interior are contaminated to a lesser degree by F, Cl and Br relative to I than those found near the coast. The measured enrichment ratio of I/F is a function of the distance between the collection site and the open sea, and increases from the Allan Hills to the Thiel Mountains. By revealing the degree of contamination of a meteorite it is possible to determine its maximum surface residence time on the Antarctic ice.  相似文献   

4.
The chemical surveillance of Kilauea volcano, Hawaii, has continued. No relationship has thus far been identified between the helium content of an associated fumarole and the activity at the volcano. Fume samples from Halemaumau crater in Kilauea caldera and from a fissure eruption that occurred nearby on the floor of the caldera during August 1971 were examined for their halogen (Cl and F) and sulfur contents. The ratio of Cl/F in fume showed an abnormal increase in samples taken at Halemaumau a month before the eruption. This change in ratio may be a helpful indicator of the onset of eruption in volcanic areas.  相似文献   

5.
Post-collapse rhyolite lava domes, lava flows and pyroclastic rocks from Valles caldera (1140 ka), erupted from 1133 ka to approximately 520-60 ka, have been sampled to study variations of light lithophile (Li, Be, B) and halogen (F, Cl) elements. Our principal objectives were: (1) to examine the mobility of these elements during post-eruptive devitrification and hydration; and (2) to study their behavior during magma differentiation. Compared to fresh glassy samples, devitrified rocks from the same dome are depleted in B, Li, F and Cl, but not in Be. During devitrification, Be was immobile while the other elements were progressively more mobile in the order B < Li < Cl < F, fluorine being the most mobile element. Considering only fresh glassy samples, Li, Be and B were enriched in residual liquids and behaved incompatibly during differentiation of successive magma batches at 973-787 ka and 557-521 ka. The rhyolites have low B/Be ratios of 2–3 which decrease slightly with increasing Be; these values suggest a small fractionation of B from Be during evolution of the magmas. While F behaves like the light lithophile elements, Cl shows (1) much smaller temporal enrichment during differentiation at 973-787 ka and (2) depletion with time from 557 to 521 ka. At the same time, the Cl/Be ratio declines progressively from ˜250 in the oldest rhyolites to ˜ 100 in the youngest rhyolites. These data suggest that (1) a magmatic fluid phase continuously extracted Cl from fluid-saturated magmas and (2) some of the magmatic Cl lost could have been incorporated into the Valles hydrothermal system.  相似文献   

6.
Magma degassing at Soufrière Hills Volcano (SHV) is characterised by an almost permanent SO2 flux and a HCl production rate which mainly depends on dome growth rate. Degassing processes have been studied through textural, H2O and halogen analyses of clasts collected between 1995 and 2006 on the dome and in pyroclastic flows and vulcanian eruption deposits. Cl, Br and I are strongly depleted in melts during H2O degassing with no significant Cl–Br–I fractionation, whereas F is almost unaffected. All magmas erupted at SHV have followed a multi-step degassing path from the magma chamber up to a shallow depth ( 1 km, P  20 MPa). From that depth, however, effusive and explosive paths are distinct; vulcanian eruptions are the result of closed system degassing (CSD), while effusive dome growth is the result of CSD up to a very shallow depth (≤ 200 m, P  5–2 MPa) followed by open system degassing (OSD). CSD is modelled using the H2O solubility law, the perfect gas law and partition coefficients of halogens between a rhyolitic melt and H2O vapour (dv − li). Gas loss characteristic of OSD is modelled using a Rayleigh law. Degassing induced crystallisation is introduced through the ratio of crystallisation and degassing rates, which ranges from 150–500. dv − lCl for OSD ranges between 50–300, increasing with melt Cl content. For CSD, the lower effective dv − lCl ( 20) is attributed to kinetic effects.

Dome forming activity has a greater impact on atmospheric chemistry than vulcanian eruptions because OSD is much more efficient at extracting halogens. The model shows that HCl flux is a good proxy for the dome forming eruption rate. Comparison between model and measured gas compositions suggests a high HBr–BrO conversion rate (BrO/Total Br  1/3) in the SHV gas plume.

The degassing behaviour of Cl, Br and I implies similar Cl/Br ( 160) and Br/I ( 90) in initial melts, volcanic clasts and high temperature gases. The low Cl/Br at SHV compared to other island arcs ( 250–300) is attributed to a shallow, pre-eruptive Br enrichment. The almost permanent dome extrusion at SHV since 1995 has likely had a significant regional atmospheric impact because of the very efficient effusive degassing and the high conversion rate of halogens into reactive species within the gas plume.  相似文献   


7.
We have constructed an artificial laboratory fumarole to calibrate the most common chemical volcanic gas sampling techniques and obtain a quantitative measure of their efficacy. We have also developed and tested a new rugged and portable venturi spray gas sampler. The venturi sampler reproduced the output gas composition most accurately, followed by the Giggenbach bottles, filter packs, and lastly alkaline traps. Passive alkaline traps, however, did better than filter packs when sampling more concentrated fumarole gases. Under ideal conditions, the accuracy of the Giggenbach bottles was identical to the venturi sampler, although there was slightly more scatter. The Giggenbach sampler was more susceptible to problems with condensation on the input train even in a laboratory setting, and this technique was only effective in relatively concentrated gas streams. Filter packs are also effective, but extreme care must be exercised to maintain strong undersaturation with respect to the acid gas. If strong undersaturation (high pH) is not maintained, the filter packs return erroneously low S/Cl and S/F ratios. Use of a pH indicator is an effective way of avoiding this problem. The passive alkaline traps also under-sample sulfur, resulting in low reported S/Cl and S/F ratios. It appears that the overall sampling efficiency of all techniques was not strongly affected by oxygen fugacity over the limited range tested. When detecting sulfate and sulfite simultaneously, we found no difference in total sulfur before and after oxidation. This suggests that all sulfur from the gas regardless of oxidation state was absorbed as sulfite or sulfate and/or was quickly oxidized in solution. This conclusion is supported by IC HS− reference samples.  相似文献   

8.
This paper deals with sulfur, chlorine and fluorine abundances in the eruptive volcanic plume of the huge October 2002-January 2003 eruption of Mount Etna, aiming at relating the relevant compositional variations observed throughout with changes in eruption dynamics and degassing mechanisms. The recurrent sampling of plume acidic volatiles by filter-pack methodology revealed that, during the study period, S/Cl and Cl/F ratios ranged from 0.1-6.8 and 0.9-5.6, respectively. Plume S/Cl ratios increased by a factor of ∼10 as volcanic activity drifted from paroxysmal lava fountaining (mid- and late November) to passive degassing and minor effusion (early January), and then decreased to the low values (S/Cl=0.1) typical of the final stages of the eruption. Parallel variations in chlorine to fluorine ratios were also observed. A theoretical model is proposed for quantitative interpretation of these changes in plume composition. The model calculates the composition of a volatile phase exsolving from an ascending Etna magma, based on knowledge of solubilities and abundances in the undegassed melt of sulfur and halogens [T.M. Gerlach, EOS 72 (1991), 249, 254-255]. According to this model, degassing of Etnean basaltic melt at high pressures and depths (>100 MPa, 3 km) is likely to release a CO2+H2O-rich vapor phase with S/Cl molar ratios ∼1. Extensive sulfur and chlorine degassing from the melt would take place at shallower depth (P<20 MPa, 0.6 km), with S/Cl ratios in the vapor phase increasing as pressure drops to 0.1 MPa. Comparisons between model compositions and volcanic plume data demonstrate that the chemical trends observed during the eruption may be explained by increased degassing due to depressurization of a basaltic magma batch ascending toward the surface.  相似文献   

9.
On six occasions, Irom July 1971 to June 1973, discharge samples from twelve selected fumaroles on White Island in the Bay of Plenty, New Zealand, were collected and analysed. The large variations in the absolute and relative proportions of carbon, sulfur, and chlorine containing species, occurring simultaneously over the entire active area of the volcano, suggest that all fumaroles are essentially supplied with one common type of gas made up of at least three components. During quiet periods, with low fumarolic outlet temperatures (≤300), the component with ratios C:S:Cl of 92:3:5 predominates; during heating up periods the relative carbon contents decrease, considered to be due to admixture of a component with C:S:Cl ratios of 44:26:30. Coinciding with maximum outlet temperatures (≈ 800°), however, the component with C:S:Cl ratios of 70:29:1 predominates, causing a rapid and marked rise in the ratio S:Cl from unity to above ten. The latter component with low ratios of C:S of around 2.5 and ratios of S:Cl of above ten is considered to be most closely related to the primary magmatic gas phase.  相似文献   

10.
Hawaiian volcanoes characteristically have but few of the many types of minerals found in incrustations of other volcanic areas. In Hawaii sulfates resulting from air oxidation of volatiles predominate, and fluorides produced during rock alteration by fumarolic gases are prominent. Halides are generally found where reducing conditions exist in fumaroles and lava lake drill holes. The most common mineral types are sulfur, opaline silica, gypsum, ralstonite, and thenardite. Minerals from the same deposit are found to vary markedly in the content of the less abundant components. Condensates from vapor issuing from fumaroles show little quantitative relationship in component content to incrustations deposited at the same fumaroles. It is believed that an energetically favorable isomorphic substitution of some elements in the crystal lattice of a depositing mineral may lead to the build-up of a high concentration of an element from a lean vapor. Equilibrium calculations applied to condensate studies give a good quantitative approximation to the concentrations of the elements found in natural systems, but when applied to incrustations they serve only to indicate general compositional relations. Laboratory studies have shown the important role of chlorides in metal transfer in the gas phase in high-temperature aqueous systems, but only in the absence of oxygen. These studies also demonstrated the important role of HF in rock alteration and in the transfer of silica.  相似文献   

11.
We investigated the distribution of Cl, F, Li, and Be in pumices, obsidians, and crystallized dome rocks at Chaitén volcano in 2008?C2009 in order to explore the behavior of these elements during explosive and effusive volcanic activity. Electron and ion microprobe analyses of matrix and inclusion glasses from pumice, obsidian, and microlite-rich dome rock indicate that Cl and other elements were lost primarily during crystallization of the rhyolitic dome after it had approached the surface. Glass in pumice and microlite-free obsidian has 888?±?121?ppm Cl, whereas residual glass in evolved microlite-rich dome rock generally retains less Cl (as low as <100?ppm). Estimated Cl losses were likely >0.7?Mt Cl, with a potential maximum of 1.8?Mt for the entire 0.8-km3 dome. Elemental variations reflect an integrated bulk distribution ratio for Cl?>?1.7 (1.7 times more Cl was degassed or incorporated into crystals than remained in the melt). Because Cl is lost dominantly as the very last H2O is degassed, and Cl is minimally (if at all) partitioned into microlites, the integrated vapor/melt distribution ratio for Cl exceeds 200 (200 times more Cl in the evolved vapor than in the melt). Cl is likely lost as HCl, which is readily partitioned into magmatic vapor at low pressure. Cl loss is accelerated by the change in the composition of the residual melt due to microlite growth. Cl loss also may be affected by open-system gas fluxing. Integrated vapor-melt distribution ratios for Li, F, and Be all exceed 1,000. On degassing, an unknown fraction of these volatiles could be immediately dissolved in rainwater.  相似文献   

12.
Pre-eruptive conditions and degassing processes of the AD 79 plinian eruption of Mt. Vesuvius are constrained by systematic F and Cl measurements in melt inclusions and matrix glass of pumice clasts from a complete sequence of the pumice-fallout deposits. The entire ‘white pumice’ (WP) magma and the upper part of the ‘grey pumice’ (GP) magma were saturated relative to sub-critical fluids (a Cl-rich H2O vapour phase and a brine), with a Cl melt content buffered at ~ 5300 ppm, and a mean H2O content of ~ 5%. The majority of the GP magma was not fluid-saturated. From these results it can be estimated that the WP magma chamber had a low vertical extent (< 500 m) and was located at a depth of ~ 7.5 km while the GP magma reservoir was located just beneath the WP one, but its vertical extent cannot be constrained. This is approximately two times deeper than previous estimates. H2O degassing during the WP eruption followed a typical closed-system evolution, whereas GP clasts followed a more complex degassing path. Contrary to H2O, Cl was not efficiently degassed during the plinian phase of the eruption.

This study shows that F and Cl behave as incompatible elements in fluid-undersaturated phonolitic melts. H2O saturation is necessary for a significant partitioning of Cl into the fluid phase. However, Cl cannot be extracted in significant quantity from phonolitic melts during rapid H2O degassing, e.g. during plinian eruptions, due to kinetics effects. Halogen contents are better preserved in volcanic glass (melt inclusions or matrix glass) than H2O, therefore the combined analysis of both volatile species is required for reliable determination of pre-eruptive conditions and syn-eruptive degassing processes in magmas stored at shallow depths.  相似文献   


13.
Abstract
Determination of chemical constituent ratios allows distinction between two salinization mechanisms responsible for shallow saline ground water and vegetative-kill areas in parts of west Texas. Mixing of deep-basin (high Cl) salt water and shallow (low Cl) ground water results in saline waters with relatively low Ca/Cl, Mg/Cl, SO44/ Cl, Br/Cl, and NO3/Cl ratios. In scattergrams of major chemical constituents vs. chloride, plots of these waters indicate trends with deep-basin brines as high Cl end members. Evaporation of ground water from a shallow water table, in contrast, results in saline water that has relatively high Ca/Cl, Mg/Cl, SO4/Cl, and Br/CL ratios. Trends indicated by plots of this water type do not coincide with trends indicated by plots of sampled brines. Leaching of soil nitrate in areas with a shallow water table accounts for high NO3 concentrations in shallow ground water.  相似文献   

14.
Mafic and ultramafic intrusions in East Greenland adjacent to the offshore Greenland–Iceland ridge were emplaced 5–9 My after continental breakup at 55 Ma [1]. Rare earth element (REE) concentrations determined by secondary ion mass spectrometry are reported for cumulus clinopyroxene from these intrusions, and the data are used to estimate REE abundance in equilibrium melts using available partitioning data. Estimated equilibrium melts from intrusions have strongly fractionated REE patterns with Nd/Dy(N) in the range 2 to 5.6 and Yb/Dy(N) 0.55 to 0.92, similar to values for coeval basalts. These melts have markedly higher Nd/Dy(N) than earlier breakup related flood basalts. The moderately low Yb/Dy(N) for the post-breakup volcanism is indicative of residual garnet in the source, while their high Nd/Dy(N) ratios can best be explained by aggregating low degree melts from a light-REE-enriched garnet- and spinel-bearing mantle source. We also report He, Sr, and Nd isotopic data for the intrusions. The highest 3He/4He ratios (>10 R/Ra) are found in the samples whose REE data reflect the largest proportion of melts from a garnet-bearing source, and having Sr and Nd isotopic compositions identical with the radiogenic Sr and unradiogenic Nd isotope end of the Iceland compositional field. There is no indication of a MORB-type mantle in the source of the intrusions. We postulate that post-breakup volcanism along the East Greenland coastline reflects the increasing proximity of the mantle plume to the East Greenland continental margin. The low degree of melting at high mean pressure inferred for the parental melts for the intrusions may reflect re-thickening of the lithosphere, which in turn was caused by the vigorous volcanism during breakup, with accompanying depletion of upper mantle and underplating of the crust at the continental margin.  相似文献   

15.
Cenozoic volcanic activity started in southwestern Bolivia during the Oligocene. From the Early Miocene up to the Holocene, volcanism produced about 8000 km3 of lavas and pyroclastic rocks. Five major cycles could be distinguished.North—south-trending fissures in the eastern part of southwestern Bolivia were sources of Miocene ignimbrites. The eruptive centers of Pliocene ignimbrites are scattered throughout the investigated area, but are concentrated in the western part. During Pleistocene times small ignimbrite flows were formed by collapse of composite volcanoes.The oldest lavas (Oligocene) are alkaline and differ considerably from younger rocks, which are rhyodacites and dacites with only a small limited range of compositions. Based on the K2O/Na2O ratios and the mineralogical composition, the lavas can be subdivided into a calc-alkaline and a high-K calc-alkaline (shoshonitic) association. Hornblende is absent from lavas with high K2O/Na2O ratios.In southwestern Bolivia a westward migration of volcanic activity is apparent. The potassium content of the lavas decreases from the Miocene to the Holocene, whereas the sodium content increases. The potassium content cannot, therefore, be correlated with the depth of the Benioff zone. It is suggested, that the lavas and ignimbrites were formed by partial melting of material from different crustal levels.  相似文献   

16.
Chlorine and fluorine were measured from whole-rock samples from tholeiites (150,000 years old) to present-day hawaiites. The overall range of F content is from 240 to 985 ppm, with a slight decrease of F/Th and F/Cl ratios, from tholeiites to hawaiites. Chlorine is positively correlated with Th (Cl/Th=100) as well as K2O and P2O5, as the differentiation progresses, and, increases from 220 ppm in tholeiites to 2410 ppm in mugearites. Data obtained from present-day hawaiites indicate that Cl lost by degassing during eruption is limited. However, Cl contents of some whole-rock samples are inconsistent with previous results published for melt inclusions of phenocrysts from the same historic hawaiite samples and suggesting outgassing of Cl prior to the eruption. This implies that apparent correlation between Cl and Th can be considered as the result of superimposition of several petrogenetic processes. Results point out the richness of Etnean tholeiites in chlorine compared to M.A.R. basalts. Such a character could have been inherited from the mantle source or during the mantle source melting.  相似文献   

17.
A new apparatus, Venturi Effect System (VES), designed for sampling volcanic plumes is described and tested at Vulcano (Italy). This device, together with purified basic NH4OH solutions, supplies optimal conditions to obtain reliable Stotal/Cl/F ratios and enrichment factors for metallic trace elements (MTE). Good concordance for acid gas ratios and metal enrichment factors in both the gas phase and the related plume allows the procedure to be validated. The VES appears in Vulcano conditions as a simple, robust and easily portable apparatus that allows reliable collection of both acid gases and MTE within a single sample and the analysis with current chemical methods (High Pressure Liquid Chromatography, Inductively Coupled Plasma–Mass Spectrometry). This apparatus may be suitable for more difficult volcanoes where only the plume can be sampled.  相似文献   

18.
Marie A  Vengosh A 《Ground water》2001,39(2):240-248
One of the major problems in the lower Jordan Valley is the increasing salinization (i.e., chloride content) of local ground water. The high levels of salinity limit the utilization of ground water for both domestic and agriculture applications. This joint collaborative study evaluates the sources and mechanisms for salinization in the Jericho area. We employ diagnostic geochemical fingerprinting methods to trace the potential sources of the salinity in (1) the deep confined subaquifer system (K2) of Lower Cenomanian age; (2) the upper subaquifer system (K1) of Upper Cenomanian and Turonian ages; and (3) the shallow aquifer system (Q) of Plio-Pleistocene ages. The chemical composition of the saline ground water from the two Cenomanian subaquifers (K1 and K2) point to a single saline source with Na/Cl approximately 0.5 and Br/Cl approximately 7 x 10(-3). This composition is similar to that of thermal hypersaline spring that are found along the western shore of the Dead Sea (e.g., En Gedi thermal spring). We suggest that the increasing salinity in both K1 and K2 subaquifers is derived from mixing with deep-seated brines that flow through the Rift fault system. The salinization rate depends on the discharge volume of the fresh meteoric water in the Cenomanian Aquifer. In contrast, the chemical composition of ground water from the Plio-Pleistocene Aquifer shows a wide range of Cl- (100-2000 mg/L), Na/Cl (0.4-1.0), Br/Cl (2-6 x 10(-3)), and SO4/Cl (0.01-0.4) ratios. These variations, together with the high SO4(2-), K+, and NO3- concentrations, suggest that the salinity in the shallow aquifer is derived from the combination of (1) upconing of deep brines as reflected by low Na/Cl and high Br/Cl ratios; (2) leaching of salts from the Lisan Formation within the Plio-Pleistocene Aquifer, as suggested by the high SO4(2-) concentrations; and (3) anthropogenic contamination of agriculture return flow and sewage effluents with distinctive high K+ (80 mg/L) and NO3- (80 mg/l) contents and low Br/Cl ratios (2 x 10(-3)). Our data demonstrates that the chemical composition of salinized ground water can be used to delineate the sources of salinity and hence to establish the conceptual model for explaining salinization processes.  相似文献   

19.
Helium isotopic ratios ranging from 20 to 32 times the atmospheric 3He/4He(RA) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the 3He/4He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower 3He/4He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 RA), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium.Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low 3He/4He) helium.3He/4He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in 3He/4He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 RA) helium with some (variable) component of lithospheric contamination added during “breakthrough”, while the later stages are characterized by a relaxation toward lithospheric 3He/4He ratios (～ 8 RA) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in 3He/4He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume.  相似文献   

20.
The Tiefosi granitic pluton is located 5 km northwest of Xinyang City,northern Dabie Orogen,and was emplaced in the Proterozoic Qinling Group. SHRIMP zircon U-Pb dating suggests its crystallization at 436 ± 11 Ma. It is composed of monzogranite and syenogranite containing some amounts of muscovite and few mafic minerals. The rocks are characterized by high and restricted SiO2 content,low FeO,Fe2O3 and MgO contents,high K2O/Na2O ratio,and display high-K calc-alkaline and peraluminous (ACNK>1.1) characteristics. They are generally enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE). They can be divided into three groups in light of rare earth elements (REE) and trace elements. Group I is moderate in ΣREE and characterized by the absence of Eu anom-aly,high (La/Yb)N ratio,and moderate Rb/Sr and Rb/Ba ratios. Group Ⅱ has moderately negative Eu anomaly,low (La/Yb)N ratio and high ΣREE contents,Rb/Sr and Rb/Ba ratios. Group Ⅲ displays positive Eu anomaly,moderate (La/Yb)N ratio,and low ΣREE,Rb/Sr and Rb/Ba ratios. The calculated εNd(440Ma) values of the rocks vary from 8.8 to 9.9 and Nd depleted mantle model ages are about 2.0 Ga,which resemble those of the paragneisses from the Qinling Group. The results indicate that the Tiefosi granite is crust-derived,syn-collisional S-type granite. Generation of Group I was related to low degree melting of the Qinling Group,while Group Ⅱ was formed by fractionational crystallization of plagioclase from Group I magmas,and Group Ⅲ resulted possibly from magma mingling with plagioclase cumulates. The Tiefosi granite was formed within crustal level related to the collision between the North China and South China blocks in the Early Paleozoic time.  相似文献   

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