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1.
The results of a Sr isotopic study of coexisting alkaline silicate rocks and carbonatites of two Cretaceous alkaline complexes of India, Amba Dongar (Deccan Flood Basalt Province) and Sung Valley (Rajmahal–Bengal–Sylhet Flood Basalt Province) are reported. The overlapping nature of initial Sr isotopic ratios of alkaline rocks and carbonatites of both the complexes is consistent with a magmatic differentiation model. Modelling of initial 87Sr/86Sr variation in alkaline rocks of Amba Dongar is consistent with a process of crustal assimilation by the parent magma undergoing simultaneous fractional crystallization of silicate rocks and silicate–carbonate melt immiscibility. A maximum of ∼5% crustal contamination has been estimated for the parent magma of Amba Dongar, the effect of which is not seen in the Sr isotope ratio of carbonatites generated by liquid immiscibility. A two point Rb–Sr isochron of the Sung Valley carbonatites, pyoxenite and a phlogopite from a carbonatite yielded an age of 106±11 Ma, which is identical to the 40Ar–39Ar age of this complex. The same age for the carbonatites and the alkaline silicate rocks, similar initial Sr ratios and the higher Sr concentration in the former than the latter favour the hypothesis of liquid immiscibility for the generation of the Sung Valley. The higher initial 87Sr/86Sr ratio for these complexes than that of the Bulk Earth indicates their derivation from long-lived Rb/Sr-enriched sources.  相似文献   

2.
Rocks of the northeast portion of the Colorado mineral belt form two petrographically, chemically and geographically distinct rock suites: (1) a silica oversaturated granodiorite suite; and (2) a silica saturated, high alkali monzonite suite. Rocks of the granodiorite suite generally have Sr contents less than 1000 ppm, subparallel REE patterns and initial 87Sr/ 86Sr ratios greater than 0.707. Rocks of the monzonite suite are restricted to the northeast part of the mineral belt, where few rocks of the granodiorite suite occur, and generally have Sr contents greater than 1000 ppm, highly variable REE patterns and 87Sr/86Sr initial ratios less than 0.706.Despite forming simple, smooth trends on major element variation diagrams, trace element data for rocks of the granodiorite suite indicate that they were not derived from a single magma. These rocks were derived from magmas having similar REE patterns, but variable Rb and Sr contents, and Rb/Sr ratios. The preferred explanation for these rocks is that they were derived by partial melting of a mixed source, which yielded pyroxene granulite or pyroxenite residues.The monzonite suite is chemically and petrographically more complex than the granodiorite suite. It is subdivided here into alkalic and mafic monzonites, and quartz syenites, based on the textural relations of their ferromagnesian phases and quartz. The geochemistry of these three rock types require derivation from separate and chemically distinct magma types. The preferred explanation for the alkalic monzonites is derivation from a heterogeneous mafic source, leaving a residue dominated by garnet and clinopyroxene. Early crystallization of sphene from these magmas was responsible for the severe depletion of the REE observed in the residual magmas. The lower Sr content and higher Rb/Sr ratios of the mafic monzonites requires a plagioclase-bearing source.The Sr-isotope systematics of the majority of these rocks are interpreted to be largely primary, and not the result of crustal contamination. The positive correlation of Rb/Sr and 87Sr/86Sr ratios for the least fractionated samples indicate that the sources from which parent magmas of both the granodiorite and monzonite suites were derived are Precambrian in age.  相似文献   

3.
Two suites of felsic eruptives and intrusives are represented in a set of samples from the summit region of the Plio-Pleistocene volcano, Mt. Kenya. Most of the samples are moderately or strongly undersaturated and have 87Sr/86Sr initial ratios in the range 0.70360–0.70368 (mean=0.70362). Members of this phonolitic suite are phonolites, nepheline syenites or kenytes and as a group they show a wide variation in TiO2, FeO, P2O5, Sr, Ba, Zr and Nb. The minor and trace element geochemistry reflect variation in the nature of the parental basaltic magmas from which the phonolitic rocks evolved and variation in the crystal fractionation process in individual cases. Crystal fractionation involving plagioclase, alkali feldspar, clinopyroxene, olivine and magnetite is the process by which most of the phonolitic rocks evolved and variation in the relative proportions of these phases in individual cases has led to a broad spectrum of trace and minor element behaviour. The second suite of felsic samples is critically saturated and consists of trachytes showing either slight oversaturation or slight undersaturation with respect to SiO2. This trachyte suite has lower initial 87Sr/86Sr ratios (mean=0.70355) and is derived from transitional alkalic basalts by low pressure (crustal) crystal fractionation involving feldspar, clinopyroxene, magnetite and olivine. The range in minor and trace element chemistry observed among the felsic rocks is a consequence of variation in the parental basalts which is related to mantle source variation and to the specific nature of the crystal fractionation process.  相似文献   

4.
Carbonatites are believed to have crystallized either from mantle-derived primary carbonate magmas or from secondary melts derived from carbonated silicate magmas through liquid immiscibility or from residual melts of fractional crystallization of silicate magmas. Although the observed coexistence of carbonatites and alkaline silicate rocks in most complexes, their coeval emplacement in many, and overlapping initial87Sr/86Sr and143Nd/144Nd ratios are supportive of their cogenesis; there have been few efforts to devise a quantitative method to identify the magmatic processes. In the present study we have made an attempt to accomplish this by modeling the trace element contents of carbonatites and coeval alkaline silicate rocks of Amba Dongar complex, India. Trace element data suggest that the carbonatites and alkaline silicate rocks of this complex are products of fractional crystallization of two separate parental melts. Using the available silicate melt-carbonate melt partition coefficients for various trace elements, and the observed data from carbonatites, we have tried to simulate trace element distribution pattern for the parental silicate melt. The results of the modeling not only support the hypothesis of silicate-carbonate melt immiscibility for the evolution of Amba Dongar but also establish a procedure to test the above hypothesis in such complexes.  相似文献   

5.
Results of different isotopic and trace element studies on three carbonatite–alkaline complexes (Amba Dongar, Mundwara and Sarnu-Dandali) of the Deccan flood basalt province, India, are presented. The Amba Dongar (Ambadungar) complex has been dated precisely to 65.0±0.3 Ma by the 40Ar–39Ar method. The minimum initial Sr isotopic ratio of alkaline rocks of Amba Dongar is found to be same as that of the coexisting carbonatites, suggesting their derivation from a common parent magma, probably through liquid immiscibility. The rare earth element abundance in these rocks also supports the liquid immiscibility hypothesis. Further investigation revealed that the parent magma of this complex has been contaminated (∼5%) by the lower crustal material, which is clearly reflected in the initial 87Sr/86Sr variation of alkaline rocks but not in the carbonatites. Sr study also suggests that the mantle source of Amba Dongar like the other two complexes is a Rb/Sr enriched source. The temporal and spatial relationships of all the three complexes with the Deccan flood basalts support the hypothesis of reunion plume origin for these. Fractional crystallization and subsequent hydrothermal/meteoric alteration are found to have controlled the stable carbon and oxygen isotopic variations in carbonatites. This study suggests that all the complexes have been derived from isotopically average mantle except for a particular batch of parent magma at Amba Dongar, which appears to have incorporated recycled crustal carbon. In a plume origin scenario such incorporation indicates the entrainment of 13C-enriched subcontinental lithospheric mantle by the plume.  相似文献   

6.
Whole-rock Rb-Sr isochron dating of Sn-bearing granites and alkaline rocks from Gejiu, Yunnan Province has been conducted for their emplacement ages and initial87Sr/86Sr ratios. The Sr isotopic compositions of apatites from some basic rocks in Jiasha, and granite bodies also have been studied in detail. The genesis and evolution of Gejiu Sn-bearing granites as well as ore-search indicators are discussed on the basis of the available data in conjunction with the geochemical data on trace elements (such as Rb and Sr), Sr isotopic characteristics of the volcanic rocks, meta-diabase and host rocks and the isotopic features of ore leads.  相似文献   

7.
G.G. Pe  A. Gledhill 《Lithos》1975,8(3):209-214
Isotopic ratios of strontium in 9 volcanic rocks from the south-eastern part of the Hellenic arc range from 0.7037 to 0.7075. Within individual series of differentiation, there seems to be a correlation between Sr87/Sr86 and K2O/SiO2.All strontium isotope data for the Hellenic arc are reviewed. Comparable (but slightly smaller) ranges of Sr isotope ratios are found in other island arcs with continental basement. To explain the high values of Sr87/Sr86 ratio for the Hellenic arc, a selective addition of Sr87 from the wall rock, and a process of assimilation involving water, perhaps from subducted sediments, are suggested. Since closely-spaced individual volcanic centres of similar ages have very different Sr isotope ratios, and since the range of Sr isotopic composition in individual centres is quite large, the variation is unlikely to be due to primary variation in mantle composition.  相似文献   

8.
Geological mapping, petrography, geochemistry, and isotope studies enable the division of the Pelotas Batholith into six granitic suites: Pinheiro Machado (PMS), Erval (ES), Viamão (VS), Encruzilhada do Sul (ESS), Cordilheira (CS), and Dom Feliciano (DFS). The rocks of the PMS show a large compositional range (granite through granodiorite to tonalite), and the suite is considered pre- to syncollisional. Other suites show restricted compositional variations (granite to granodiorite) and are late to postcollisional. In general, the suites are metaluminous to slightly peraluminous (PMS, ES, and VS) or peraluminous (CS) or have alkaline tendencies (ESS and DFS). The magmatic evolution corresponds to high-K calc-alkaline to alkaline magmatism. The suites are enriched in K, Rb, and REE compared with rocks of typical calc-alkaline series. Initial 87Sr/86Sr ratios vary from 0.705 to 0.716, except in the CS, where they attain values of 0.732–0.740. Sm–Nd TDM model ages vary between 0.98 and 2.0 Ga, with initial εNd values ranging from −0.3 to −10. U–Pb zircon dates of samples from PMS, VS, and ESS suggest an age between 0.63 and 0.59 Ga for magmatism. Rb–Sr dates of samples of alkaline granites from DFS present ages between 0.57 and 0.55 Ga. The main tectonic controls of the magmatism of the Pelotas Batholith are high-dip sinistral shear zones.  相似文献   

9.
Major‐ and trace‐element chemistry (including rare‐earth elements), total‐rock Rb‐Sr and U‐Pb and zircon U‐Pb data are used in an attempt to distinguish between two essentially coeval, felsic volcanic suites: the predominantly submarine Woodlawn suite which is associated with massive Cu‐Pb‐Zn sulphide mineralization and the terrestrial Mt Painter suite, with minor vein‐type mineralization. The Woodlawn samples are the unmineralized equivalents of the volcanics in the immediate ore environment.

Alteration perturbs some of the major‐ and trace‐element chemistry, particularly Ca and alkalis, thereby precluding their usefulness. REE patterns exhibit a significant light to heavy rare‐earth enrichment with an average La/Yb of 12 in the Mt Painter volcanics compared with 5.6 in the Woodlawn volcanics. Both suites have a marked negative Eu anomaly, with that of the Woodlawn samples more pronounced (‐45.5) than in the Mt Painter volcanics (‐29.2). A hydrothermally‐altered sample from Woodlawn has apparently lost about 50% of its light rare‐earth elements.

Initial 87Sr/86Sr ratios at about 0.711 are the same for rocks from both suites and differences in initial lead‐isotopic ratios appear negligible.

Zircons from both suites are a mixture of clear euhedral crystals and rounded discrete crystals or rounded cores overgrown by clear zircon. The U‐Pb data substantiate the morphological features in that the zircon suites both contain older inherited Pb but the Mt Painter zircons contain a greater proportion.

Cs concentrations and Cs/Rb and Ti/Zr ratios can be used to distinguish between the Woodlawn suite and the Mt Painter suite.  相似文献   

10.
The 87Sr/86Sr ratios have been determined on the volcanic rocks of Ustica, Linosa and Pantelleria Islands. The petrology of these islands is typical of volcanic products belonging to the alkalic suite. The volcanites of Ustica and Linosa Islands are mainly represented by basic terms (alkalibasalts and hawaiites), with minor mugearitic and trachytic differentiates. In addition to alkali-basalts and hawaiites, also some alkaline and peralkaline rocks of Pantelleria have been isotopically analysed. The 87Sr/86Sr ratios are consistent with a subcrustal origin for all the volcanic products of these islands. Some differences in the 87Sr/86Sr ratios have been found and tentatively related to an inhomogeneous Rb/Sr distribution in the mantle source material. The genetic relationships of these rocks with some products of the recent Tyrrhenian volcanism are also briefly discussed.  相似文献   

11.
Nd and Sr isotope data were obtained for three plutonic suites (595–505 Ma) and distinct young granitoid intrusions (503 Ma), from the southern part of the Neoproterozoic Araçuaí Orogen. The Sr and Nd isotopes (87Sr/86Sr, eNd) and TDM values from the plutons and distinct basement rocks are used to constrain the magma genesis of the granitoid plutons. These isotopic parameters, with eNd values ranging from −4 to −24 and TDM ages from 1.3 to 2.8 Ga, for the granitoid suites, and −5 to −40 and 3.5 to 1.5 Ga, for the distinct Archean and Proterozoic basement complexes, suggest that the Jequitinhonha Complex metasediments are the main crustal source for most of these plutons, except for the youngest granitoid intrusions, which may have a protolith similar to the Mantiqueira and Guanhães complexes. Furthermore, the isotope data indicate a minor, but important, participation of Neoproterozoic oceanic lithosphere in the granite genesis, which corroborates with a confined orogenic model and a narrow oceanic consumption (B-subduction) for the Araçuaí Orogen.  相似文献   

12.
The two world’s largest complexes of highly alkaline nepheline syenites and related rare metal loparite and eudialyte deposits, the Khibina and Lovozero massifs, occur in the central part of the Kola Peninsula. We measured for the first time in situ the trace element concentrations and the Sr, Nd and Hf isotope ratios by LA-ICP-MS (laser ablation inductively coupled plasma mass spectrometer) in loparite, eudialyte an in some other pegmatitic minerals. The results are in aggreement with the whole rock Sr and Nd isotope which suggests the formation of these superlarge rare metal deposits in a magmatic closed system. The initial Hf, Sr, Nd isotope ratios are similar to the isotopic signatures of OIB indicating depleted mantle as a source. This leads to the suggestion that the origin of these gigantic alkaline intrusions is connected to a deep seated mantle source—possibly to a lower mantle plume. The required combination of a depleted mantle and high rare metal enrichment in the source can be explained by the input of incompatible elements by metasomatising melts/fluids into the zones of alkaline magma generation shortly before the partial melting event (to avoid ingrowth of radiogenic isotopes). The minerals belovite and pyrochlore from the pegmatites are abnormally high in 87Sr /86Sr ratios. This may be explained by closed system isotope evolution as a result of a significant increase in Rb/Sr during the evolution of the peralkaline magma.  相似文献   

13.
Initial 87Sr/86Sr ratios have been plotted against time of formation for various rock-types in the Schwarzwald and Vosges basement areas. These data exhibit strong positive correlations between the two variables. The Schwarzwald data define two distinct trend lines on the diagram, for the time span 500 to 250 Ma ago. The first comprises the data from orthogneisses, diatexites and pre-tectonic granites and documents the Sr isotope evolution in the crust underlying the Sehwarzwald. This region of the crust had a 87Rb/86Sr ratio of about 1. The other is delineated by data points from the post-tectonic plutons. These form a band corresponding to the development of closed systems with 87Rb/86Sr ratios of between 10 and 20 as indicated by the slope of the band. The second trend is interpreted as resulting from the formation of large, stable, deep-seated magma chambers formed by segregation of anatectic melts during a phase of tectonism 330Ma ago. The high 87Rb/86Sr ratios of these magmas arose by fractional crystallization, in response to tectonic decompression, during the coalescence of the presumedly water-saturated melts. Data for rocks from the Vosges, taken from the literature, form a single development line. Its slope corresponds to a 87Rb/86Sr ratio of about 5 and the line is analogous to the second trend line defined by the Schwarzwald data. The differences in the Rb/Sr systematics between the two areas can be explained as resulting from the deeper level of erosion in the Vosges. An important implication for Rb/Sr studies is that co-magmatic rocks can have very different initial 87Sr/86Sr ratios so that discrepancies in this ratio between rock-types cannot be used to divide plutons into genetic suites. On the other hand essential information is contained in the Rb/Sr systematics of orogenic magmatic rocks, such as the Variscan plutons in the Schwarzwald, that cannot be obtained from geochemical and petrological studies alone.  相似文献   

14.
The Palaeo-Tethyan tectonic evolution of central Tibet remains a topic of controversy. Two Permian to Late Triassic arc-like volcanic suites have been identified in the eastern Qiangtang (EQ) block of north-central Tibet. Three competing models have been proposed to explain the formation of these volcanic suites, with two models involving a single stage of long-lived subduction but with opposing subduction polarities, while the other model involves a two-stage subduction process. Here, we present new whole-rock geochemistry, including Sr–Nd isotope data, for late Permian felsic volcanics of the Zaduo area. These volcanics are mainly low to middle K calc-alkaline felsic tuffs and rhyolites with SiO2 concentrations up to 73 wt.%. In primitive mantle-normalized diagrams, the volcanics are typified by large ion lithophile element enrichment and high-field-strength element (e.g. Nb, Ta, P, and Ti) depletion, with slightly negative Eu anomalies. They have initial Sr ratios (87Sr/86Sr) i of 0.70319–0.70547, and ?Nd(t) values of +3.4 to +3.5, suggesting derivation by the partial melting of a depleted mantle wedge, followed by assimilation of crustal material. The available geochemical data indicate the presence of two distinctive igneous evolution trends within the Permian to Late Triassic volcanics of the EQ block, consistent with a two-stage subduction model. Permian to Early Triassic arc-like volcanics are formed during northward (present-day orientation) subduction, whereas the Late Triassic volcanics are related to southward (present-day orientation) subduction of mafic crust of the Garze–Litang Ocean.  相似文献   

15.
The debate about whether Eocene magmatism is considered to be post-collisional or subduction-related or not still continues. Here we offer new 40Ar-39Ar ad U-Pb zircon geochronology, mineral chemistry, bulk rock and Sr-Nd-Pb isotope geochemistry data obtained from the southern dike (SD) suite, in comparison with the northern dike (ND) suite, from the Eastern Pontides. The geochronological data indicate that the SD suite erupted between 45.89 and 45.10 Ma corresponding to the Lutetian (Middle Eocene). The magmas of the ND suite are characterised by slightly more alkaline affinity compared to the SD suite. The trace and rare earth element (REEs) content of the SD suite is characterised by large ion lithophile element (LILEs; Sr, K2O, Ba, Rb) enrichment and depletion of Nb, Ta, and TiO2 elements to different degree with high Th/Yb ratios, which indicate that the magmas forming the SD and ND suites were derived from lithospheric mantle sources enriched by mostly slab-derived fluids in the spinel stability field. The Sr, Nd and Pb radiogenic isotope ratios of the dikes support the view that the magma for the hydrous group (H-SD) was derived from a relatively more enriched mantle source than the other SD and ND suites. The ND suite and the anhydrous group (A-SD) display similar geochemical features characterised by moderate light earth element (LREE)/heavy rare earth element (HREE) ratios, while the H-SD group has respectively lower LREE/HREE ratios indicating higher melting degree. Detailed considerations of the alkalinity, enrichment and partial melting degree for the source of the studied volcanic rocks indicate that the magmas of the northern dike suite are characterised by slightly more alkaline affinity, whereas the magmas throughout the southern dike suite show increments in the enrichment rate and melting degree. In light of the obtained data and comparative interpretations, the geodynamic evolution and differences in petrogenetic character of the Lutetian magmas from both the northern and southern parts of the Eastern Pontides may be explained by different degrees of melting of a net veined mantle source initially metasomatized by mostly subduction fluids during asthenospheric upwelling due to fragmented asymmetric delamination in a post-collisional extensional tectonic environment.  相似文献   

16.
Two “S-type” (pelitic) granite suites from the New England Batholith, N.S.W., have Upper Carboniferous ages, indicating that they predate by 40 m.y. the intrusion of hornblende biotite granites, and are the oldest plutons of the batholith. Mineralogically and geochemically both suites have “pelitic” characteristics, one suite containing an Al-rich biotite, muscovite and cordierite, the other an Al-rich biotite and rare pyrope-almandine garnet. Low initial 87Sr/86Sr ratios of 0.706 for both suites probably reflect the volcanoclastic nature and young age of the sedimentary source of these granites at the time of melting. The age of the suites coincides with the last stages of (Andean type?) volcanism along an andesite/dacite volcanic chain to the west, suggesting an origin for the “S-type” granitic magma by partial melting of deformed sediments marginal to a continental region.  相似文献   

17.
Sixty-four Rb-Sr and two K-Ar isotopic measurements from seven ring complexes in central Nigeria provide evidence for a systematic age trend along a 200 km zone ranging from 174±5 m.y. in the north to 154±4 m.y. in the south. A peak of anorogenic magmatism occurred in the Jos Plateau region about 164±4 m.y. ago. Although a small syenitetrachyte complex at Zaranda, near Bauchi, gives an age of 190±15 m.y., unpublished ages of 290–330 m.y. for the southern Niger ring complexes confirm the existence of an overall southerly decreasing age trend in the Niger-Nigeria province of West Africa. Isotopic measurements on two small, oversaturated syenite intrusions at Zaranda and Pankshin suggest that syenitic liquids had initial 87Sr/86Sr ratios of 0.7048—not significantly different from the mantle range of values, but that related peralkaline silicic variants from the same complexes are depleted in total Sr and have higher 87Sr/86Sr initial ratios characteristic of the earth's crust. This variation of initial 87Sr/86Sr ratios in syenite-related granitic liquids of the peralkaline spectrum has also been noted at the Shere Hills, near Jos, and at Liruei, near Kano, and may be representative for all syenite-granite occurrences in the Nigerian Younger Granite province. Such isotopic variations in the initial 87Sr/86Sr ratio may be attributed to “crustal enrichment” of syenitic liquids whose source lies in the mantle. Coarse-grained, peraluminous biotite granites have consistently low initial 87Sr/86Sr ratios in the range 0.706–0.709 (similar to the ca. 600 m.y. Pan-African granites of the basement), and may represent further modifications of originally syenitic liquids in the crust, or the granites may have originated from an independent source within a “dioritio” lower crust. Although the magmatic trends show small variations in the initial 87Sr/86Sr ratio, much higher initial ratios are recorded in granites which have been modified within their roof zone by deuteric (autometamorphic) and/or metasomatic processes.  相似文献   

18.
Isotope ratios and elemental concentrations in otoliths are often used as natural tags to reconstruct migratory movements and connectivity patterns in marine and anadromous fishes. Although differences in otolith geochemistry have been documented among geographically separated populations, inter-annual variation within locations is less frequently examined. We compared otolith isotope (δ18O and 87Sr:86Sr) and elemental ratios (Sr:Ca and Ba:Ca) from several annual cohorts of juvenile American shad (Alosa sapidissima) in three rivers. These four geochemical signatures distinguished among river-specific populations of this species at both large and small geographic scales, with δ18O and 87Sr:86Sr generating the majority of multivariate variation. We found significant variation among years for all variables in two to three rivers. However, the magnitude of variability differed among ratios, with δ18O ratios showing substantial inter-annual shifts while 87Sr:86Sr ratios were relatively stable across years. Sr:Ca and Ba:Ca ratios also varied among years. These results imply that investigators using environmentally labile signatures must quantify geochemical signatures for each cohort of interest in order to confidently identify origins of migrants.  相似文献   

19.
A 4-yr study of spatial and temporal variability in the geochemistry of vadose groundwaters from caves within the Edwards aquifer region of central Texas offers new insights into controls on vadose groundwater evolution, the relationship between vadose and phreatic groundwaters, and the fundamental influence of soil composition on groundwater geochemistry. Variations in Sr isotopes and trace elements (Mg/Ca and Sr/Ca ratios) of dripwaters and soils from different caves, as well as phreatic groundwaters, provide the potential to distinguish between local variability and regional processes controlling fluid geochemistry, and a framework for understanding the links between climatic and hydrologic processes.The Sr isotope compositions of vadose cave dripwaters (mean 87Sr/86Sr = 0.7087) and phreatic groundwaters (mean 87Sr/86Sr = 0.7079) generally fall between values for host carbonates (mean 87Sr/86Sr = 0.7076) and exchangeable Sr in overlying soils (mean 87Sr/86Sr = 0.7088). Dripwaters have lower Mg/Ca and Sr/Ca ratios, and higher 87Sr/86Sr values than phreatic groundwaters. Dripwater 87Sr/86Sr values also inversely correlate with both Mg/Ca and Sr/Ca ratios. Mass-balance modeling combined with these geochemical relationships suggest that variations in fluid compositions are predominantly controlled by groundwater residence times, and water-rock interaction with overlying soils and host aquifer carbonate rocks. Consistent differences in dripwater geochemistry (i.e., 87Sr/86Sr, Mg/Ca, and Sr/Ca) between individual caves are similar to compositional differences in soils above the caves. While these differences appear to exert significant control on local fluid evolution, geochemical and isotopic variations suggest that the controlling processes are regionally extensive. Temporal variations in 87Sr/86Sr values and Mg/Ca ratios of dripwaters from some sites over the 4-yr interval correspond with changes in both aquifer and climatic parameters. These results have important implications for the interpretation of trace element and isotopic variations in speleothems as paleoclimate records, as well as the understanding of controls on water chemistry for both present-day and ancient carbonate aquifers.  相似文献   

20.
The Quaternary alkaline volcanic field of Southern Turkey is characterized by intra-continental plate-type magmatic products, exposed to the north of the ?skenderun Gulf along a NE-SW trending East Anatolian Fault, to the west of its intersection with the N–S trending Dead Sea Fault zone. The ?skenderun Gulf alkaline rocks are mostly silica-undersaturated with normative nepheline and olivine and are mostly classified as basanites and alkaline basalts with their low-silica contents ranging between 43 and 48?wt.% SiO2. They display Ocean Island Basalt (OIB)–type trace element patterns characterized by enrichments in large-ion-lithophile elements (LILE) and light rare earth element (LREE), and have (La/Yb)N?=?8.8–17.7 and (Hf/Sm)N?=?0.9–1.6 similar to those of basaltic rocks found in intraplate suites. The basanitic rocks have limited variations Sr-Nd isotopic ratios (87Sr/86Sr?=?0.70307–0.70324, 143Nd/144Nd?=?0.512918–0.521947), whereas the alkali basalts display more evolved Sr-Nd isotopic ratios (87Sr/86Sr?=?0.70346-0.70365, 143Nd/144Nd?=?0.512887–0.521896). The ?skenderun Gulf alkaline rocks also display limited Pb isotopic variations with 206Pb/204Pb?=?18.75–19.09 207Pb/204Pb?=?15.61–15.66 and208Pb/204Pb?=?38.65–39.02, indicating that they originated from an enriched lithospheric mantle source. Calculated fractionation vectors indicate that clinopyroxene and olivine are the main fractionating mineral phases. Similarly, based on Sr-Nd isotopic ratios, the assimilation and fractional crystallization (AFC) modeling shows that the alkali basalts were affected by AFC processes (r?=?0.2) and were slightly contaminated by the upper crustal material.The high TiO2 contents, enrichments in Ba and Nb, and depletions in Rb can likely be explained by the existence of amphibole in the mantle source, which might, in turn, indicate that the source mantle has been affected by metasomatic processes. The modeling based on relative abundances of trace elements suggests involvement of amphibole-bearing peridotite as the source material. ?skenderun Gulf alkaline rocks can thus be interpreted as the products of variable extent of mixing between melts from both amphibole-bearing peridotite and dry peridotite.  相似文献   

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