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1.
This study of the Pikes Peak batholith includes the mineralogy and petrology of quartz syenite at West Creek and of fayalite-bearing and fayalite-free biotite granite near Mount Rosa; major element chemistry of the batholith; comparisons with similar postorogenic, intracratonic, sodic to potassic intrusives; and genesis of the batholith.The batholith is elongate in plan, 50 by 100 km, composite, and generally subalkalic. It was emplaced at shallow depth 1,040 m. y. ago, sharply transects its walls and may have breached its roof. Biotite granite and biotite—hornblende granite are predominant; quartz syenite, fayalite granite and riebeckite granite are present in minor amounts.Fayalite-bearing and fayalite-free quartz syenite, fayalite-biotite granite and riebeckite granite show a well-defined sodic differentiation trend; the less sodic fayalite-free granites exhibit a broader compositional range and no sharp trends.Crystallization was largely at PH2O < Ptotal; PH2O approached Ptotal only at late stages. Aplite residual to fayalite-free biotite granite in the north formed at about 1,500 bars, or 5 km depth. Feldspar assemblages indicate late stages of crystallization at about 720°C. In the south ilmenite and manganian fayalite indicate fO2 of 10?17 or 10?18 bars. Biotite and fayalite compositions and the ‘granite minimum’ imply completion of crystallization at about 700°C and 1,500 bars. Nearby fayalite-free biotite granite crystallized at higher water fugacity.All types of syenite and granite contain 5–6% K2O through a range of SiO2 of 63–76%. Average Na2O percentages in quartz syenite are 6.2, fayalite granite 4.2, and fayalite-free granite 3.3 MgO contents are low, 0.03–0.4%; FeO averages 1.9–2.5%. FeO/Fe2O3 ratios are high. Fluorine ranges from 0.3 to 0.6%.The Pikes Peak intrusives are similar in mode of emplacement, composition, and probably genesis to rapakivi intrusives of Finland, the Younger Granites of Nigeria, Cape Ann Granite and Beverly Syenite, Mass., and syenite of Kungnat, Greenland, among others — allowing for different levels of erosion. A suite that includes gabbro or basalt, anorthosite, quartz syenite, fayalite granite, riebeckite granite, and biotite and/or hornblende granites is of worldwide occurrence.A model is proposed in which mantle-derived, convecting alkali olivine basaltic magma first reacts with K2O-poor lower crust of granulite facies to produce magma of quartz syenitic composition. The syenitic liquid in turn reacts with granodioritic to granitic intermediate crust of amphibolite facies to produce the predominant fayalite-free biotite and biotite-hornblende granites of the batholith. This reaction of magma and roof involves both partial melting and the reconstitution and precipitation of refractory phases, as Bowen proposed. Intermediate liquids include MgO-depleted and Na2O-enriched gabbro, which precipitated anorthosite, and alkali diorite. The heat source is the basaltic magma; the heat required for partial melting of the roof is supplied largely by heats of crystallization of phases that settle out of the liquid — mostly olivine, clinopyroxene and plagioclase.  相似文献   

2.
Based on the experiments on dehydration-melting of solid samples of Al-rich gneiss (H029) and biotite granulitite (H013), the fugacities of O2, H2O and H2 have been calculated. It is recognized that the fugacities of O2, H2O and H2 vary regularly, but the fugacity of H2O shows a tendency of abrupt increasing at about 700°C and 800°C. According to the above fact, the melting mechanism of biotite can be well documented. Under relatively low temperatures (< 750°C), part of the water can be liberated and induce plagioclase to melt, which may mark the beginning of migmatization. At high temperatures (> 800°C), biotite can be dissociated and a larger amount of water can be released, which would result in a bigger degree of melting, hence leading to the formation of granitic magma.  相似文献   

3.
Differentiation of mantle-derived, hydrous, basaltic magmas is a fundamental process to produce evolved intermediate to SiO2-rich magmas that form the bulk of the middle to shallow continental and island arc crust. This study reports the results of fractional crystallization experiments conducted in a piston cylinder apparatus at 0.7 GPa for hydrous, calc-alkaline to arc tholeiitic magmas. Fractional crystallization was approached by synthesis of starting materials representing the liquid composition of the previous, higher temperature experiment. Temperatures ranged from near-liquidus at 1,170 °C to near-solidus conditions at 700 °C. H2O contents varied from 3.0 to more than 10 wt%. The liquid line of descent covers the entire compositional range from olivine–tholeiite (1,170 °C) to high-silica rhyolite (700 °C) and evolves from metaluminous to peraluminous compositions. The following crystallization sequence has been established: olivine → clinopyroxene → plagioclase, spinel → orthopyroxene, amphibole, titanomagnetite → apatite → quartz, biotite. Anorthite-rich plagioclase and spinel are responsible for a marked increase in SiO2-content (from 51 to 53 wt%) at 1,040 °C. At lower temperatures, fractionation of amphibole, plagioclase and Fe–Ti oxide over a temperature interval of 280 °C drives the SiO2 content continuously from 53 to 78 wt%. Largest crystallization steps were recorded around 1,040 °C and at 700 °C. About 40 % of ultramafic plutonic rocks have to crystallize to generate basaltic–andesitic liquids, and an additional 40 % of amphibole–gabbroic cumulate to produce granitic melts. Andesitic liquids with a liquidus temperature of 1,010 °C only crystallize 50 % over an 280 °C wide range to 730 °C implying that such liquids form mobile crystal mushes (<50 % crystals) in long-lived magmatic systems in the middle crust, allowing for extensive fractionation, assimilation and hybridization with periodic replenishment of more mafic magmas from deeper magma reservoirs.  相似文献   

4.
The crystallization sequence of a basaltic andesite from Bezymianny Volcano, Kamchatka, Russia, was simulated experimentally at 100 and 700 MPa at various water activities (aH2O) to investigate the compositional evolution of residual liquids. The temperature (T) range of the experiments was 950–1,150 °C, aH2O varied between 0.1 and 1, and the log of oxygen fugacity (fO2) varied between quartz–fayalite–magnetite (QFM) and QFM + 4.1. The comparison of the experimentally produced liquids and natural samples was used to constrain the pressure (P)–T–aH2O–fO2 conditions of the Bezymianny parental magma in the intra-crustal magma plumbing system. The phase equilibria constraints suggest that parental basaltic andesite magmas should contain ~2–2.5 wt% H2O; they can be stored in upper crustal levels at a depth of ~15 km, and at this depth they start to crystallize at ~1,110 °C. The subsequent chemical evolution of this parental magma most probably proceeded as decompressional crystallization occurred during magma ascent. The final depths at which crystallization products accumulated prior to eruption are not well constrained experimentally but should not be shallower than 3–4 km because amphibole is present in natural magmas (>150 MPa). Thus, the major volume of Bezymianny andesites was produced in a mid-crustal magma chamber as a result of decompressional crystallization of parental basaltic andesites, accompanied by mixing with silicic products from the earlier stages of magma fractionation. In addition, these processes are complicated by the release of volatiles due to magma degassing, which occurs at various stages during magma ascent.  相似文献   

5.
This study presents a pre-eruptive magma storage model for the rhyodacite and andesite magmas erupted during the 3430 yBP caldera-forming eruption of Aniakchak volcano, Alaska, derived from phase equilibria experiments and petrological data. The compositions of Fe–Ti oxide pairs from the early erupted Plinian rhyodacite pumice yield core temperatures of 871–900°C, with rims up to ∼942°C, and fO2 from −10.6 to −11.8 log units. Melt inclusions entrapped in plagioclase phenocrysts have H2O contents between 3 and 5 wt%, estimated by FTIR and electron microprobe volatiles by difference methods, with no detectable CO2. Assuming water saturation, this corresponds to entrapment pressures between ∼65 and 150 MPa. Phase equilibria results reproduce the natural phase assemblages at of 95–150 MPa at 870–880°C, assuming water saturation. A mismatch in experimental versus natural glass SiO2 and Al2O3, and MELTS models for H2O-undersaturated conditions indicate that the rhyodacite may not have been H2O saturated. MELTS models with and P total of 125–150 MPa at 870–880°C reproduce the natural groundmass glass Al2O3 composition best, indicating the magma may have been slightly H2O undersaturated. Those pressures correspond to storage at 4.5–5.4 km depth in the crust. MELTS models and VBD estimates from melt inclusions in titanomagnetite grains from the andesite indicate pre-eruptive conditions of ∼1,000°C and > 110 MPa, corresponding to a minimum residence depth of ∼4.1 km assuming water saturation or greater if the magma was H2O undersaturated. Previous geochemical studies indicate separate histories of the two magmas, though they retain some evidence that they are ultimately related through fractional crystallization processes. Analogous to the 1912 Novarupta magmas, the rhyodacite and andesite presumably originated within the same crystal mush zone beneath the edifice, yet were separated laterally and underwent different degrees of crustal assimilation. The andesite must have resided in close proximity, with ascent occurring in response to movement of the rhyodacite, and resulting in extensive syn-eruptive mingling.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.  相似文献   

6.
The areally extensive (>5000 km2), syn-tectonic, ca. 520 Ma, mainly S-type Donkerhuk batholith was constructed through injection of thousands of mainly sheet-like magma pulses over 20–25 Myr. It intruded schists of the Southern Zone accretionary prism in the Damara Belt of Namibia. Each magma pulse had at least partly crystallised prior to the arrival of the following batch. However, much of the batholith may have remained partially molten for long periods, close to the H2O-saturated granite solidus. The batholith shows extreme variation in chemistry, while having limited mineralogical variation, and seems to be the world’s most heterogeneous granitic mass. The Nd model ages of ~2 Ga suggest that Eburnean rocks of the former magmatic arc, structurally overlain by the accretionary wedge, are the most probable magma sources. Crustal melting was initiated by mantle heat flux, probably introduced by thermal diffusion rather than magma advection. The granitic magmas were transferred from source to sink, with minimal intermediate storage; the whole process having occurred in the middle crust, resulting in feeble crustal differentiation despite the huge volume of silicic magma generated. Source heterogeneity controlled variation in the magmas and neither mixing nor fractionation was prominent. However, due to the transpressional emplacement régime, local filter pressing formed highly silicic liquids, as well as felsic cumulate rocks. The case of the Donkerhuk batholith demonstrates that emplacement-level tectonics can significantly influence compositional evolution of very large syn-tectonic magma bodies.  相似文献   

7.
Most igneous charnockites are interpreted to have crystallized at hot and dry conditions, i.e. at >800?°C and <3 wt.% H2O and with an important CO2 component in the system. These charnockites are metaluminous to weakly peraluminous and their formation involves a significant mantle-derived component. This study, in contrast, investigates the crystallization conditions of strongly peraluminous, metasediment-sourced charnockites from the Qinzhou Bay Granitic Complex, South China. To constrain the temperature-melt H2O crystallization paths for the studied peraluminous charnockites, petrographic characterization was combined with fluid inclusion compositional data, mineral thermometry, and thermodynamic modelling. The uncertainties of the thermodynamic modelling in reconstructing the crystallization conditions of the granitic magmas have been evaluated by comparison between modelled and experimental phase relations for a moderately evolved, peraluminous granite (~70 wt.% SiO2). The comparison suggests that the modelling reproduces the experimentally derived phase saturation boundaries with uncertainties of 20–60?°C and 0.5–1 wt.% H2O for systems with ≤1–2 wt.% initial melt H2O at ~0.2 GPa. For the investigated natural systems, the thermometric estimates and modelling indicate that orthopyroxene crystallized at relatively low temperature (750–790?±?30?°C) and moderately high to high melt H2O content (3.5–5.6?±?0.5 wt.%). The charnockites finally solidified at relatively “cold” and “wet” conditions. This suggests that thermodynamic modelling affords a possible approach to constrain charnockite crystallization as tested here for peraluminous, moderately low pressure (≤0.3 GPa), and overall H2O-poor systems (≤1–2 wt.% H2O total), but yields results with increasing uncertainty for high-pressure or H2O-rich granitic systems.  相似文献   

8.
The high-K, calcalkaline granitic rocks of the 370 Ma, post-orogenic Harcourt batholith in southeastern Australia have I-type affinities but are mildly peraluminous and have remarkably radiogenic isotope characteristics, with 87Sr/86Srt in the range 0.70807 to 0.714121 and εNdt in the range ??5.6 to ??4.3. This batholith appears to be a good example of magmas that were derived through partial melting of distinctly heterogeneous source rocks that vary from intermediate meta-igneous to mildly aluminous metasedimentary rocks, with the balance between the two rock types on the metasedimentary side. Such transitional S-I-type magmas, formed from mainly metasedimentary source rocks, may be more common than is generally realised. The Harcourt batholith also contains mainly granodioritic igneous microgranular enclaves (IMEs). Like their host rocks, the IMEs are peraluminous and have rather radiogenic isotope signatures (87Sr/86Srt of 0.71257–0.71435 and εNdt of ??7.3 to ??4.3), though some are hornblende-bearing. Origins of these IMEs by mixing a putative mantle end member with the host granitic magma can be excluded because of the variability in whole-rock isotope ratios and, for the same reason, the IME magmas cannot represent quench cumulates (autoliths) from the host magmas. Less abundant monzonitic to monzosyenitic IMEs cannot represent accumulations of magmatic biotite and/or alkali feldspar because K-feldspar is absent, and there is no co-enrichment of K2O and FeO?+?MgO, nor can they be mixtures of anything plausible with the host-rock magma. The granodioritic IMEs probably originated through high degrees of assimilation of a range of crustal materials (partial melts?) by basaltic magmas in the deep crust, and the monzonitic IMEs as melts of enriched subcontinental mantle. Such enclave suites provide little or no information on the chemical evolution of their host granitic rocks.  相似文献   

9.
The formation of ore-bearing granites in the Yenshanian movement in southeast China and the geochemical characteristics of some RE-bearing granites have been studied through multivariate statistical analysis and physicochemical approach. The main conclusions have Been drawn as follows: (1) The granites are believed to be products of anatexis of the crustal materials. The formation temperature of granitic magma is estimated at about 600°C and the crystallization temperatures range from 600° to 500°C. The temperature of Li-, Fand H2O-rich residual magma in the latest stage of magmatism is probably below 500°C. (2) A rock series from early lepidomelane-granite through protolithionite-and zinnwalditegranite to lithioniteor lepidolite-granite is considered as a result of actual crystallization. (3) The mineral paragenesis and fades zonation of granite plutons are mainly controlled by Ph2o, μNa2O and μK2O in the magma. (4) During the magmatic evolution the ore-forming elements (REE, Nb, Ta, etc.) are variable in geochemistry. REEs, similar to mafic components, were highly concentrated at the early stage of the magmatic evolution and deposited under favourable conditions in the zinnwaldite-and protolithionite-granites; Nb and Ta have a preference for felsic and volatile components, thus are mainly concentrated at later stages of the magmatic evolution. Nb ore deposits are formed in the lithionite and lepidolite granites, for Ta is intimately associated with Na2O, Li2O, F and H2O.  相似文献   

10.
A small body of mafic texturally and compositionally varied igneous intrusive rocks corresponding to redwitzites occurs at Abertamy in the Western pluton of the Krušné hory/Erzgebirge granite batholith (Czech Republic). It is enclosed by porphyritic biotite granite of the older intrusive suite in the southern contact zone of the Nejdek-Eibenstock granite massif. We examined the petrology and geochemistry of the rocks and compared the data with those on redwitzites described from NE Bavaria and Western Bohemia.The redwitzites from Abertamy are coarse- to medium-grained rocks with massive textures and abundant up to 2 cm large randomly oriented biotite phenocrysts overgrowing the groundmass. They are high in MgO, Cr and Ni but have lower Rb and Li contents than the redwitzites in NE Bavaria. Compositional linear trends from redwitzites to granites at Abertamy indicate crystal fractionation and magma mixing in a magma chamber as possible mechanisms of magma differentiation. Plots of MgO versus SiO2, TiO2, Al2O3, FeO, CaO, Na2O, and K2O indicate mainly plagioclase and orthopyroxene fractionation as viable mechanisms for in situ differentiation of the redwitzites.The porphyritic biotite monzogranite enclosing the redwitzite is the typical member of the early granitic suite (Older Intrusive Complex, OIC ) with strongly developed transitional I/S-type features. The ages of zircons obtained by the single zircon Pb-evaporation method suggest that the redwitzites and granites at Abertamy originated during the same magmatic period of the Variscan plutonism at about 322 Ma.The granitic melts have been so far mainly interpreted to be formed by heat supply from a thickened crust or decompression melting accompanying exhumation and uplift of overthickened crust in the Krušné hory/Erzgebirge due to a previous collisional event at ca. 340 Ma. The presence of mafic bodies in the Western pluton of the Krušné hory/Erzgebirge batholith confirms a more significant role of mantle-derived mafic magmas in heating of the sources of granitic melts than previously considered.  相似文献   

11.
The investigation of rocks, minerals, and melt inclusions showed that porphyritic alkaline picrites and meimechites crystallized from different parental magmas. At a similar ultrabasic composition, the alkaline picrite melts were enriched in K2O relative to Na2O, and contained up to 0.12–0.13 wt % F and less Cr, Ni, and H2O (only 0.01–0.16 wt % H2O, versus 0.6–1.6 wt % in the meimechite melts) compared with the meimechite magmas. The crystallization of alkaline picrite melts occurred under stable conditions at relatively low temperatures without abrupt changes: olivine and clinopyroxene crystallized at 1340–1285 and 1230–1200°C, respectively, as compared with 1600–1450 and 1230–1200°C in the meimechites. The alkaline picrite melts evolved toward melanephelinite, nephelinite, tephrite, and trachydolerite; whereas the meimechite magmas gave rise to subalkaline picritic rocks. The partitioning of vanadium between olivine and melt suggests that the meimechite magma crystallized under more oxidizing conditions compared with the alkaline picrite melts: the KDV values for the meimechite melts (0.011–0.016) were three times lower than those for the alkaline picrite melts (0.045–0.052). The parental magmas of the alkaline picrites and meimechites were enriched in trace elements relative to mantle levels by factors of tens to hundreds. The alkaline picrite magma showed lower LILE and LREE contents compared with the meimechite magma. The magmas had also different indicator ratios of incompatible elements, including those immobile in aqueous fluids. It was concluded that the meimechite and alkaline picrite melts were derived from different mantle sources. The former were generated at lower degrees of melting of an undepleted mantle source, and the meimechite melts were produced by high-degree melting of a probably lherzolite-harzburgite source.  相似文献   

12.
The Vinalhaven intrusive complex provides field and petrographic evidence for multiple replenishments of mafic and silicic magmas, mingling and limited mixing, and rejuvenation of granite. Quartz in granitic rocks preserves a record of those processes, in the form of cathodoluminescence (CL) zoning, which is related to concentration of titanium, and to temperature of crystallization using the new TitaniQ (Ti in quartz) geothermometer. Injection of mafic melts into partly crystalline Vinalhaven granite resulted in partial quartz resorption followed by higher-temperature growth from H2O-undersaturated melt. This is shown by steep, rimward increases in CL intensity and Ti content across discordant boundaries that truncate older growth zones. Quartz zoning in granite affected by mafic magmas displays large rimward jumps in Ti content, whereas quartz in granitic feeders and in granite far from mafic rocks typically displays broad rims with decreasing Ti contents, consistent with slow cooling without thermal disruptions due to mafic recharge.  相似文献   

13.
Dacites dominate the large-volume, explosive eruptions in magmatic arcs, and compositionally similar granodiorites and tonalites constitute the bulk of convergent margin batholiths. Shallow, pre-eruptive storage conditions are well known for many dacitic arc magmas through melt inclusions, Fe–Ti oxides, and experiments, but their potential origins deeper in the crust are not well determined. Accordingly, we report experimental results identifying the P–T–H2O conditions under which hydrous dacitic liquid may segregate from hornblende (hbl)-gabbroic sources either during crystallization–differentiation or partial melting. Two compositions were investigated: (1) MSH–Yn?1 dacite (SiO2: 65 wt%) from Mount St. Helens’ voluminous Yn tephra and (2) MSH–Yn?1?+?10% cpx to force saturation with cpx and map a portion of the cpx?+?melt?=?hbl peritectic reaction boundary. H2O-undersaturated (3, 6, and 9 wt% H2O) piston cylinder experiments were conducted at pressures, temperatures, and fO2 appropriate for the middle to lower arc crust (400, 700, and 900 MPa, 825–1100?°C, and the Re–ReO2 buffer?≈?Ni–NiO?+?2). Results for MSH–Yn?1 indicate near-liquidus equilibrium with a cpx-free hbl-gabbro residue (hbl, plg, magnetite, ± opx, and ilmeno-hematite) with 6–7 wt% dissolved H2O, 925?°C, and 700–900 MPa. Opx disappears down-temperature consistent with the reaction opx?+?melt?=?hbl. Cpx-added phase relations are similar in that once ~10% cpx crystallizes, multiple saturation is attained with cpx, hbl, and plg, +/? opx, at 6–7 wt% dissolved H2O, 940?°C, and 700–900 MPa. Plg–hbl–cpx saturated liquids diverge from plg–hbl–opx saturated liquids, consistent with the MSH–Yn?1 dacite marking a liquid composition along a peritectic distributary reaction boundary where hbl appears down-temperature as opx?+?cpx are consumed. The abundance of saturating phases along this distributary peritectic (liquid?+?hbl?+?opx?+?cpx?+?plg?+?oxides) reduces the variance, so liquids are restricted to dacite–granodiorite–tonalite compositions. Higher-K dacites than the Yn would also saturate with biotite, further limiting their compositional diversity. Theoretical evaluation of the energetics of peritectic melting of pargasitic amphiboles indicates that melting and crystallization of amphibole occur abruptly, proximal to amphibole’s high-temperature stability limit, which causes the system to dwell thermally under the conditions that produce dacitic compositions. This process may account for the compositional homogeneity of dacites, granodiorites, and tonalites in arc settings, but their relative mobility compared to rhyolitic/granitic liquids likely accounts for their greater abundance.  相似文献   

14.
H2O-undersaturated melting experiments of synthesized basalt (SiO2 = 50.7 wt.%, MgO = 8.3 wt.%, Mg# = 60) were conducted at fO2 corresponding to NNO+1 and NNO−1 to clarify the effects of pressure (2–7 kbar) and H2O on fractional crystallization in island arcs. H2O content was ranged from nominally anhydrous to 4.4 wt.%. Differentiation trends, namely the liquid lines of descent, change sensitively according to pressure-H2O relations. Tholeiitic differentiation trends are reproduced with H2O ≤ ∼2 wt.% in primary magma. With such quantities of H2O, fractional crystallization is controlled by olivine + plagioclase at 2 kbar. Increasing the pressure from 2 to ≥4 kbar induces early crystallization of orthopyroxene instead of olivine and therefore SiO2 enrichment in the residual melts is suppressed. Increasing H2O (≥ ∼2 wt.% in primary magma) stabilizes clinopyroxene relative to orthopyroxene and/or magnetite. Although the phase relations and proportions strongly depend on fO2 and H2O content, differentiation trends are always calc-alkaline.  相似文献   

15.
This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H2O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 14C years Before Present (14C years b.p.). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H2O contents of 3 to 6 wt% H2O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ∼3000 14C years b.p.) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H2O (<0.2 wt%), lower LILE abundance and different isotopic characteristics. Thus, the mantle-derived inputs into the Medicine Lake system have not always been low H2O, primitive HAOT, but have alternated between HAOT and hydrous subduction related, calc-alkaline basalt. This influx of hydrous mafic magma coincides temporally and spatially with rhyolite eruption at Glass Mountain and Little Glass Mountain. The rhyolites contain quenched magmatic inclusions similar in character to the mafic lavas at Callahan and Paint Pot Crater. The influence of H2O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H2O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO2-enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H2O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H2O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes. Received: 4 January 1999 / Accepted: 30 August 1999  相似文献   

16.
The Zhawulong granitic pegmatite lithium deposit is located in the Ganzi-Songpan orogenic belt. Fluid inclusions in spodumene and coexisting quartz were studied to understand the cooling path and evolution of fluid within albite–spodumene pegmatite. There are three distinguishable types of fluid inclusions: crystal-rich, CO2–NaCl–H2O, and NaCl–H2O. At more than 500°C and 350~480 MPa, crystal-rich fluid inclusions were captured during the pegmatitic magma-hydrothermal transition stage, characterized by a dense hydrous alkali borosilicate fluid with a carbonate component. Between 412°C and 278°C, CO2–NaCl–H2Ofluid inclusions developed in spodumene (I) and quartz (II) with a low salinity (3.3–11.9 wt%NaCl equivalent) and a high volatile content, which represent the boundary between the transition stage and the hydrothermal stage. The subsequentNaCl–H2Ofluid inclusions from the hydrothermal stage, between 189°C and 302°C, have a low salinity (1.1–13.9 wt%NaCl equivalent). The various types of fluid inclusions reveal the P–T conditions of pegmatite formation, which marks the transition process from magmatic to hydrothermal. The ore-forming fluids from the Zhawulong deposit have many of the same characteristics as those from the Jiajika lithium deposit. The ore-forming fluid provided not only materials for crystallization of rare metal minerals, such as spodumene and beryl, but also the ideal conditions forthe growth of ore minerals. Therefore, this area has favorable conditions for lithium enrichment and excellent prospecting potential.  相似文献   

17.
The 1.1 Ga Concordia Granite Gneiss (CGG) is part of the late to postorogenic Spektakel Suite in the western Namaqualand Metamorphic Complex, South Africa. It intruded synkinematically, with respect to the main (D2) deformation event, into lower to middle crustal rocks and granite emplacement was more or less coeval with the peak of granulite-facies metamorphism ( > 800°C, 5 kbar). Several genetically related rock types, megacrystic garnet-bearing granite, minor aplitic leucogranites and pegmatites are distinguished. All varieties are SiO2-rich (69–79 wt.%) peraluminous granites and show subalkaline-monzonitic magma characteristics. Geochemical differences in whole-rock chemistry between megacrystic granite and aplitic leucogranites (e.g., lower Al2O3, MgO, CaO, Ba, Zr; higher K2O, Rb, Nb, W, Rb/Sr, Ga/Al) and the decrease of e.g., CaO, MgO, Fe2O3, Ba, Zr, Th/U with increasing SiO2 in the megacrystic granites as well as the variation in Fe/Mn of magmatic garnets are best explained with crystal fractionation processes. Fractional crystallization of plagioclase produced potassium- and silica-rich residual melts characterised by very high Rb/Sr, Rb/Ba, U/Th, Mn/Fe ratios and higher concentration of W, Cu and Zn. Crystal fractionation processes also resulted in a relative LREE depletion and HREE enrichment (megacrystic granite: La/Lu)cn = 8.87−31.67; aplitic leucogranite and pegmatites: La/Lu)cn = 0.71−1.44) and evolution of pronounced negative Eu-anomalies. The crystallization sequence (near-solidus crystallization of biotite prior to alkali feldspar) suggests that the CGG magmas were H2O-undersaturated over a long period of their evolution. Water saturation during late-stage crystallization is, however, indicated by coarse late-stage eutectic mineral textures, pegmatites and WMo-bearing siliceous rocks. Furthermore the economic potential of the CGG is supported by its geochemical signature (e.g., high U, Th contents) which is similar to evolved high heat production (HHP) granites. The granitic magmas are attributed to partial melting of peraluminous crustal source rocks and are tentatively interpreted as fractionated S-type granites. The WMo deposits represent vein-type and pegmatitic deposits genetically related to a deep-seated granitic system.  相似文献   

18.
Epidote phenocrysts in dacitic dikes,Boulder County,Colorado   总被引：1，自引：0，他引：1  
Epidote (Ps21%) crystallized early as elongate phenocrysts in Late Cretaceous rhyodacitic dikes in the vicinity of Ward, Boulder County, Colorado. Other unusual phenocryst phases are garnet (Gr17–24%) and muscovite. In a xenolith containing kyanite, corundum, biotite, and plagioclase, magmatic garnet grew as a rim around xenocrystic pyrope-rich (Py37%) garnet. The xenolith was derived from a granulite-facies zone, not represented at the present-day erosion surface which is composed of upper amphibolite-facies cordierite and sillimanite-bearing gneisses. The dike magmas were fed not from an immediately underlying batholith but from a magma chamber at a depth corresponding to a pressure of 8–13 kilobars. Phenocrysts cystallized in the temperature range 800 to 700° C, under H2O and O2 activities greater than normal for silicic magmas. This occurrence shows convincingly not only that epidote can be magmatic but that it is a possible early-crystallization phase in silicic magmas.  相似文献   

19.
The paper reports data on the mineralogy, geochemistry, phase composition of comendites and pantellerites from Nemrut volcano, eastern Turkey; estimates of the crystallization conditions of minerals, composition of matrix glasses and melt inclusions in anorthoclase, fayalite, hedenbergite phenocrysts. LA-ICP-MS was applied to analyze the matrix glasses and phenocryst minerals. The distribution coefficients between phases and glass were calculated for P, B, Li, Rb, Cs, Ba, Sr, Zr, Hf, Ta, Nb, Sc, V, Cr, Ni, Cu, Pb, Th, U, Y, REE. Mass balance simulations of the comenditic and pantelleritic compositions, experimental data, data on melt inclusions are utilized to analyze the processes responsible for the derivation of the magmas, accumulation of components in them and to elucidate genetic links between the trachyte-comenditic, comenditic and pantelleritic melts. The origin of the residual comenditic and pantelleritic melts is explained by variations in the crystallization conditions of anorthoclase (dominant phase), hedenbergite, fayalite, Fe and Ti oxides in the parental trachyte-comenditic magma depending on the pressure and concentration of water dissolved in the melts. The accessory phases (REEand Sr-bearing fluorapatite and zircon) were likely involved in the fractionation of the melts. The following crystallization parameters were obtained by QUILF calculations for the hedenbergite, fayalite, and ilmenite phenocrysts (minimum values for quartz-free melts): 3 kbar, 763°C, ΔFMQ = ?1.27 for the Fe-comendites; 3.3–3.8 kbar, 715°C, ΔFMQ = ?1.8 for the pantellerites; 2.3 kbar, 748°C, ΔFMQ = ?1.16 for the low-Fe comendites. The equilibrium crystallization of anorthoclase phenocrysts in the comenditic melts proceeded at temperature ～750°C. Data on glasses of melt inclusions indicate that the comenditic and pantelleritic melts contained 1–3 wt % H2O. Analysis of literature data and estimates of the conditions under which the Nemrut magmas were derived suggest that the local chambers with H2O-undersaturated comenditic and pantelleritic melts could occur at centers of alkaline volcanism at depths within the range of 5 to 10–15 km (lithostatic pressure of 1–4 kbar), at temperatures <750°C and oxygen fugacity below the FMQ buffer.  相似文献   

20.
Peraluminous granitoid magmas are a characteristic product of ultrametamorphism leading to anatexis of aluminous metasedimentary rocks in the continental crust. The mechanisms and characteristic length-scales over which these magmas can be mobilized depend strongly on their melt fraction, because of their high viscosities. Thus, it is of fundamental importance to understand the controls exerted by pressure, temperature and bulk composition of the source material on melt productivity. We have studied experimentally the vapour-absent melting behaviour of a natural metapelitic rock and our results differ greatly from those of previous experimental and theoretical investigations of melt productivity from metamorphic rocks. Under H2O-undersaturated conditions, bulk composition of the source material is the overriding factor controlling melt fraction at temperatures on the order of 850–900° C. Granitoid melts formed in this temperature interval by the peritectic dehydration-melting reaction: $$\begin{gathered} Biotite + plagioclase + aluminosilicate + quartz \hfill \\ = melt + garnet \hfill \\ \end{gathered} $$ have a restricted compositional range. As a consequence, melt fractions will be maximized from protoliths whose modes coincide with the stoichiometry of the melting reaction. This “optimum mode” (approximately 38% biotite, 32% quartz, 22% plagioclase and 8% aluminosilicate) reflects the fact that generation of low-temperature granitoid liquids requires both fusible quartzo-feldspathic components and H2O (from hydrous minerals). Metapelitic rocks rich in mica and aluminosilicate and poor in plagioclase contain an excess of refractory material (Al2O3, FeO, MgO) with low solubility in low-temperature silicic melts, and will therefore be poor magma sources. Melt fraction varies inversely with pressure in the range 7–13 kbar, but the effect is not strong: the decrease (at constant temperature) over this pressure range is of at most 15 vol% (absolute). The liquids produced in our experiments are silicarich (68–73 wt% SiO2), strongly peraluminous (2–5 wt% normative corundum) and very felsic (MgO+FeO* +TiO2 less than 3 wt%, even at temperatures above 1000° C). The last observation suggests that peraluminous granitoids with more than 10% mafic minerals (biotite, cordierite, garnet) contain some entrained restite. Furthermore, because liquids are also remarkably constant in composition, we believe that restite separation is more important than fractional crystallization in controlling the variability within and among peraluminous granitoids. We present liquidus phase diagrams that allow us to follow the phase relationships of melting of silica-and alumina-saturated rocks at pressures corresponding to the mid- to deep-continental crust. Garnet, aluminosilicate, quartz and ilmenite are the predominant restitic phases at temperatures of about 900° C, but Ti-rich biotite or calcic plagioclase can also be present, depending on the bulk composition of the protolith. At temperatures above 950–1050° C (depending on the pressure) the restitic assemblage is: hercynitic spinel+ilmenite+quartz±aluminosilicate. Our results therefore support the concept that aluminous granulites (garnet-spinel-plagioclase-aluminosilicate-quartz) can be the refractory residuum of anatectic events.  相似文献   

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