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1.
The equilibrium phase relations of two volcanic rocks from thesubduction-related Mexican Volcanic Belt have been determinedwith an argon-pressurized internally heated vessel. One rockis the trachyandesite erupted from El Chich?n Volcano in 1982;the other is a primitive basalt erupted from Jorullo Volcanoin 1759. A simplified synthetic equivalent to the trachyandesitewas also investigated in lesser detail. All charges were saturatedwith hydrous vapor and a sulfur-bearing mineral. Temperatureranged from 800 to 1000?C, pressure from 1 to 4 kb, and fo2was controlled by four different solid oxygen buffers in a doublegold capsule configuration: fayalite-magnetite-quartz (FMQ),Ni-NiO (NNO), manganosite-hausmanite (MNH), and magnetite-hematite(MTH). Pyrrhotite was the only sulfur-bearing mineral observed in chargesbuffered under FMQ and NNO, whereas anhydrite crystallized underthe more oxidizing MNH or MTH; both of these observations areconsistent with those of earlier workers. With increasing temperatureand pressure, SiO2 and K2O decreased in the experimental melts,whereas Al2O3 and CaO increased. Sulfur solubility in silicatemelts was low (<0?1 wt% equivalent SOt3) for pyrrhotite-saturatedcharges, but significantly greater (to 1?3 wt.% SOt3) when anhydritewas present. Sulfur solubility in anhydrite-saturated meltsshowed strong positive dependence on both temperature and Pvapor. Sulfur amounted to some 2?5 wt.% (SOt3) of the total ejectaduring the 1982 El Chich?n eruptions, and the original magmaticsulfur content was in the range 1?25–2–5 wt% SOt3.Extrapolations of experimental temperature and pressure dependencesfor sulfur solubility indicate that such concentrations couldbe contained in a hydrous, oxidized, basaltic parent melt generatedunder Benioff zone conditions. During ascent through the uppermantle and crust, the sulfur solubility limit of the melt wouldcontinuously decrease; in response, most of the sulfur wouldbe transferred from the melt to anhydrite crystals and a separategas phase. Trachyandesite pumices erupted from El Chich?n in1982 contained both pyrrhotite and anhydrite at a temperatureof 800?C. The composition of the natural pyrrhotite yieldedan fo2 estimate 1 log unit above the NNO buffer. Based on compositionalvariations in the experimental melts with temperature and pressure,the composition of the matrix glass in the 1982 pumices indicatesequilibration of the magmatic liquid at about Ptotal=Pvapor=2kb just before eruption. At that time, sulfur in El Chich?ntrachyandesite was about equally partitioned between anhydritemicrophenocrysts and some 20 vol.% gas phase in which H2S wasprobably the dominant sulfur-bearing species. The melt thencontained only 0?05 wt.% SOt3, consistent with experimentalsolubility limits at 800?C and Pvapor=2 kb. 相似文献
2.
The equilibrium between chromite and melt has been determinedon four basalts at temperatures of 1200–1400?C over arange of oxygen fugacity (fo2) and pressures of 1 atm and 10kb. The Cr content of chromite-saturated melts at 1300?C and1 atm ranges from 0?05 wt.% Cr2O3 at a log fo2= –3 to1?4 wt.% at a log fo2=–12?8. The Cr2+/Cr3+ of melt increaseswith decreasing fo2 and is estimated by assuming a constantpartitioning of Cr3+ between chromite and melt at constant temperature.The estimated values of Cr2+/Cr3+ in the melt are at fo2 valuesof 4–5 orders of magnitude lower than the equivalent Fe2+/Fe3+values. The Cr/(Cr+Al) of chromite coexisting with melt at constanttemperature changes little with variation of fo2 below log fo2=–6.Five experiments at 10 kb indicate that Cr2O3 dissolved in themelt is slightly higher and the Cr/(Cr + Al) of coexisting chromiteis slightly lower than experiments at 1 atm pressure. Thus variationin total pressure cannot explain the large variations of Cr/(Cr+ Al) that are common to mid-ocean ridge basalt (MORB) chromite. Experiments on a MORB at 1 atm at fo2 values close to fayalite-magnetite-quartz(FMQ) buffer showed that the Al2O3 content of melt is highlysensitive to the crystallization or melting of plagioclase,and consequently coexisting chromite shows a large change inCr/(Cr + Al). It would appear, therefore, that mixing of a MORBmagma containing plagioclase with a hotter MORB magma undersaturatedin plagioclase may give rise to the large range of Cr/(Cr +Al) observed in some MORB chromite. 相似文献
3.
An Experimental Investigation of the Influence of Water and Oxygen Fugacity on Differentiation of MORB at 200 MPa 总被引：10，自引：2，他引：10
Crystallization experiments were performed at 200 MPa in thetemperature range 1150–950°C at oxygen fugacitiescorresponding to the quartz–fayalite–magnetite (QFM)and MnO–Mn3O4 buffers to assess the role of water andfO2 on phase relations and differentiation trends in mid-oceanridge basalt (MORB) systems. Starting from a primitive (MgO9·8 wt %) and an evolved MORB (MgO 6·49 wt %),crystallization paths with four different water contents (0·35–4·7wt % H2O) have been investigated. In primitive MORB, olivineis the liquidus phase followed by plagioclase + clinopyroxene.Amphibole is present only at water-saturated conditions below1000°C, but not all fluid-saturated runs contain amphibole.Magnetite and orthopyroxene are not stable at low fO2 (QFM buffer).Residual liquids obtained at low fO2 show a tholeiitic differentiationtrend. The crystallization of magnetite at high fO2 (MnO–Mn3O4buffer) results in a decrease of melt FeO*/MgO ratio, causinga calc-alkaline differentiation trend. Because the magnetitecrystallization temperature is nearly independent of the H2Ocontent, in contrast to silicate minerals, the calc-alkalinedifferentiation trend is more pronounced at high water contents.Residual melts at 950°C in a primitive MORB system havecompositions approaching those of oceanic plagiogranites interms of SiO2 and K2O, but have Ca/Na ratios and FeO* contentsthat are too high compared with the natural rocks, implyingthat fractionation processes are necessary to reach typicalcompositions of natural oceanic plagiogranites. KEY WORDS: differentiation; MORB; oxygen fugacity; water activity; oceanic plagiogranite 相似文献
4.
The Solubility of Sulphur in Hydrous Rhyolitic Melts 总被引：1，自引：1，他引：1
Experiments performed at 2 kbar, in the temperature range 800–1000°C,with fO2 between NNO–2·3 and NNO+2·9 (whereNNO is the nickel–nickel oxide buffer), and varying amountsof sulphur added to hydrous metaluminous rhyolite bulk compositions,were used to constrain the solubility of sulphur in rhyolitemelts. The results show that fS2 exerts a dominant control onthe sulphur solubility in hydrous silicate melts and that, dependingon fO2, a rhyolitic melt can reach sulphur contents close to1000 ppm at high fS2. At fO2 below NNO+1, the addition of ironto a sulphur-bearing rhyolite magma produces massive crystallizationof pyrrhotite and does not enhance the sulphur solubility ofthe melt. For a given fO2, the melt-sulphur-content increaseswith fS2. For fixed fO2 and fS2, temperature exerts a positivecontrol on sulphur solubilities, at least for fO2 below NNO+1.The mole fraction of dissolved sulphur exhibits essentiallylinear dependence on fH2S at low fO2 and, although the experimentalevidence is less clear, on fSO2 at high fO2. The minimum insulphur solubility corresponds to the redox range where bothfH2S and fSO2 are approximately equal. A thermodynamic modelof sulphur solubility in hydrous rhyolite melts is derived assumingthat total dissolved sulphur results from the additive effectsof H2S and SO2 dissolution reactions. The model reproduces wellthe minimum of sulphur solubility at around NNO+1, in additionto the variation of the sulphide to sulphate ratio with fO2.A simple empirical model of sulphur solubility in rhyoliticmelts is derived, and shows good correspondence between modeland observations for high-silica rhyolites. KEY WORDS: sulphur; solubility; rhyolite; thermodynamics; fO2; fS2 相似文献
5.
Melting and Thermal Reconstitution of Pelitic Xenoliths, Wehr Volcano, East Eifel, West Germany 总被引：3，自引：0，他引：3
Pelitic xenoliths derived from amphibolite grade basement rocksoccur within a Pleistocene, trachytic, pyroclastic unit of theWehr volcano, East Eifel, West Germany: With increasing temperatureand/or prolonged heating at high temperature, quartz-plagioclaseand micaceous layers of the xenoliths have undergone meltingto form buchites and thermal reconstitution by dehydration reactions,melting and crystallization to form restites respectively. Thexenoliths provide detailed evidence of melting, high temperaturedecomposition of minerals, nucleation and growth of new phasesand P-T-fo2 conditions of contact metamorphism of basement rocksby the Wehr magma. Melting begins at quartz-oligoclase (An17·3Ab82·3Or0·4-An20·0Ab78·1Or1·9)grain boundaries in quartz-plagioclase rich layers and the amountof melting is controlled by H2O and alkalis released duringdehydroxylation/oxidation of associated micas. Initially, glasscompositions are heterogeneous, but with increasing degreesof melting they become more homogeneous and are similar to S-typegranitic minimum melts with SiO2 between 71 and 77 wt. per cent;A/(CNK) ratios of 1·2–1·4; Na2O < 2·95and normative corundum contents of 1·9–4·0per cent. Near micas plagioclase melts by preferential dissolutionof the NaAlSi3O8 component accompanied by a simultaneous increasein CaAl2Si2O8 (up to 20 mol. per cent An higher than the bulkplagioclase composition) at the melting edge. With increasingtemperature the end product of fractional melting is the formationand persistence of refractory bytownite (An78–80) in thosexenoliths where extensive melting has taken place. Initial stage decomposition of muscovite involves dehydroxylation(H2O and alkali loss). At higher temperatures muscovite breaksdown to mullite, sillimanite, corundum, sanidine and a peraluminousmelt. Mullite (40–43 mol. per cent SiO2) and sillimanite(49 mol. per cent SiO2) are Fe2O3 and TiO2 rich (up to 6·1–0·84and 3·6–0·24 wt. per cent respectively).Al-rich mullite (up to 77 wt. per cent Al2O3) occurs with corundumwhich has high Fe2O3 and TiO2 (up to 6·9 and 2·1wt. per cent respectively). Annealing at high temperatures andreducing conditions results in the exsolution of mullite fromsillimanite and ilmenite from corundum. Glass resulting fromthe melting of muscovite in the presence of quartz is peraluminous(A/(CNK) = 1·3) with SiO2 contents of 66–69 percent and normative corundum of 4 per cent. Sanidine (An1·9Ab26·0Or72·1-An1·3Ab15·9Or82·9)crystallized from the melt. Dehydroxylation and oxidation of biotite results in a decreaseof K2O from 8·6 to less than 1 wt. per cent and oxidetotals (less H2O + contents) from 96·5 to 88·6,exsolution of Al-magnetite, and a decrease in the Fe/(Fe + Mg)ratio from 0·41 to 0·17. Partial melting of biotitein the presence of quartz/plagioclase to pleonaste, Al-Ti magnetite,sanidine(An2·0Ab34·9Or63·1) and melt takesplace at higher temperatures. Glass in the vicinity of meltedbiotite is pale brown and highly peraluminous (A/CNK = 2·1)with up to 6 wt. per cent MgO+FeO(total iroq) and up to 10 percent normative corundum. Near liquidus biotite with higher Al2O3and TiO2 than partially melted biotite crystallized from themelt. Ti-rich biotites (up to 6 wt. per cent TiO2) occur withinthe restite layers of thermally reconstituted xenoliths. Meltingof Ti-rich biotite and sillimanite in contact with the siliceousmelt of the buchite parts of xenoliths resulted in the formationof cordierite (100 Mg/(Mg+Fe+Mn) = 76·5–69·4),Al-Ti magnetite and sanidine, and development of cordierite/quartzintergrowths into the buchite melt. Growth of sanidine enclosedrelic Ca-plagioclase to form patchy intergrowths in the restitelayers. Cordierite (100 Mg/(Mg+Fe+Mn) = 64–69), quartz,sillimanite, mullite, magnetite and ilmenite, crystallized fromthe peraluminous buchite melt. Green-brown spinels of the pleonaste-magnetite series have awide compositional variation of (mol. per cent) FeAl2O4—66·6–45·0;MgAl2O4—53·0–18·7; Fe3O4—6·9–28·1;MnAl2O4—1·2–1·5; Fe2TiO4—0·6–6·2.Rims are generally enriched in the Fe3O4 component as a resultof oxidation. Compositions of ilmenite and magnetite (single,homogeneous and composite grains) are highly variable and resultfrom varying degrees of high temperature oxidation that is associatedwith dehydroxylation of micas and melting. Oxidation mainlyresults in increasing Fe3+, Al and decreasing Ti4+, Fe2+ inilmenite, and increasing Fe2+, Ti4+ and decreasing Fe3+ in associatedmagnetite. A higher degree of oxidation is reached with exsolutionof rutile from ilmenite and formation of titanhematite and withexsolution of pleonaste from magnetite. Ti-Al rich magnetite(5·1–7·5 and 8·5–13·5wt. per cent respectively) and ilmenite crystallized from meltsin buchitic parts of the xenoliths. Chemical and mineralogic evidence indicates that even with extensivemelting the primary compositions of individual layers in thexenoliths remained unmodified. Apparently the xenoliths didnot remain long enough at high temperatures for desilicationand enrichment in Al2O3, TiO2, FeO, Fe2O3, and MgO that resultsby removal of a ‘granitic’ melt, and/or by interactionwith the magma, to occur. T °C-fo2 values calculated from unoxidized magnetite/ilmenitegive temperatures ranging from 615–710°C for contactmetamorphism and the beginning of melting, and between 873 and1054°C for the crystallization of oxides and mullite/sillimanitefrom high temperature peraluminous melts. fo2 values of metamorphismand melting were between the Ni-NiO and Fe2O3-Fe3O4 buffer curves.The relative abundance of xenolith types, geophysical evidenceand contact metamorphic mineralogy indicates that the xenolithswere derived from depths corresponding to between 2–3kb Pload = Pfluid. The xenoliths were erupted during the latestphreatomagmatic eruption from the Wehr volcano which resultedin vesiculation of melts in partially molten xenoliths causingfragmentation and disorientation of solid restite layers. 相似文献
6.
Solubility of Anhydrite, CaSO4, in NaCl-H2O Solutions at High Pressures and Temperatures: Applications to Fluid-Rock Interaction 总被引：1，自引：0，他引：1
Anhydrite solubility in H2O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(XNaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H2O at 10 kbar and 800°C, CaSO4concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO4solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and XNaCl of 0·3, CaSO4 molality is 200 timeshigher than with pure H2O. Whereas CaSO4 solubility in pureH2O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all XNaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at XNaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O2 regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites 相似文献
7.
Four natural peridotite nodules ranging from chemically depletedto Fe-rich, alkaline and calcic (SiO2 = 43.7–45.7 wt.per cent, A12O3 = 1.6O–8.21 wt. per cent, CaO = 0.70–8.12wt. per cent, alk = 0.10–0.90 wt. per cent and Mg/(Mg+Fe2+)= 0.94–0.85) have been investigated in the hypersolidusregion from 800? to 1250?C with variable activities of H2O,CO2, and H2. The vapor-saturated peridotite solidi are 50–200?Cbelow those previously published. The temperature of the beginningof melting of peridotite decreases markedly with decreasingMg/(Mg+SFe) of the starting material at constant CaO/Al2O3.Conversely, lowering CaO/Al2O3 reduces the temperature at constantMg/(Mg+Fe) of the starting material. Temperature differencesbetween the solidi up to 200?C are observed. All solidi displaya temperature minimum reflecting the appearance of garnet. Thisminimum shifts to lower pressure with decreasing Mg/(Mg + Fe)of the starting material. The temperature of the beginning ofmelting decreases isobarically as approximately a linear functionof the mol fraction of H2O in the vapor (XH2Ov). The data alsoshow that some CO2 may dissolve in silicate melts formed bypartial melting of peridotite. Amphibole (pargasitic hornblende) is a hypersolidus mineralin all compositions, although its P/T stability field dependson bulk rock chemistry. The upper pressure stability of amphiboleis marked by the appearance of garnet. The vapor-saturated (H2O) liquidus curve for one peridotiteis between 1250? and 1300?C between 10 and 30 kb. Olivine, spinel,and orthopyroxene are either liquidus phases or co-exist immediatelybelow the temperature of the peridotite liquidus. The data suggest considerable mineralogical heterogeneity inthe oceanic upper mantle because the oceanic geotherm passesthrough the P/T band covering the appearance of garnet in variousperidotites. The variable depth to the low-velocity zone is explained byvariable aHjo conditions in the upper mantle and possibly alsoby variations in the composition of the peridotite itself. Itis suggested that komatiite in Precambrian terrane could formby direct melting of hydrous peridotite. Such melting requiresabout 1250?C compared with 1600?C which is required for drymelting. The genesis of kimberlite can be related to partial meltingof peridotite under conditions of XH2Ov = 0.5–0.25 (XCO2v= 0.5–0.75). Such activities of H2O result in meltingat depths ranging between 125 and 175 km in the mantle. Thisrange is within the minimum depth generally accepted for theformation of kimberlite. 相似文献
8.
Detailed laboratory study has been made on pre-Tertiary coarse-grainedglaucophane schist, garnet-epidote amphibolite, and epidoteamphibolite in the eastern slope of the Central Mountain Range,Taiwan. These petrotectonic assemblages are considered to beexotic tectonic blocks emplaced within the feebly metamorphosedin situ graphite and quartzose schists of the Yuli belt. Thinlenses of Mn-rich metamorphosed tuff are intercalated withinthe metabasaltic rocks. Such high MnO (2 wt. per cent) and lowMgO (3–4 wt. per cent) tuffaceous rocks are similar inbulk composition to some volcanic clays collected in deep oceanbasins. They consist of the characteristic assemblage Mn-bearinggarnet (5–7 wt. per cent MnO and 30 volume per cent inthe rock)+muscovite+epidote+hornblende+quartz+ albite+rutile?pyrite. Successive stages of conversion of garnet-epidote amphiboliteto blueschist assemblages were noticed. The most recrystallizedschists display abundant Mn-bearing garnet, zoned amphibole,phengite, zoned epidote, stilpnomelane, chlorite, quartz, minoralbite, magnetite, and sphene. The recrystallization processis nearly isochemical except the glaucophane schists appearto be more oxidized and contain more Na2O than the relict amphibolites.Intimately associated amphibolites of basaltic composition,in contrast, contain the assemblage hornblende+paragonite+epidote+chlorite+quartz+albite+rutile. Microprobe analyses of the coexisting minerals in glaucophaneschists, garnet-epidote amphibolites and epidote amphibolitesyield the following results: (1) garnets, consisting of almandine,spessartine, and grossular components, are less Mn and Mg-richcompared to those in in situ metabasalts of the Franciscan;(2) rim epidotes of the glaucophane schists are more pistastic(XFe=0?27–0?30) than that of the garnet-epidote amphibolite(0?2–0?22) implying higher fO2 values for the glaucophanization;(3) phengitic micas of the glaucophane schist have less Al2O3content (29 wt. per cent) than those of the garnet-epidote amphibolite(32 wt. per cent) whereas micas of epidote amphibolites areparagonites with K/(K+Na) ratio of 0?04; (4) the zoned amphibolesshow glaucophane occurring marginal to cores of calcic amphibole.Sodic amphiboles with Al2O3 of 6-? to 10?4 wt. per cent arecrossite-glaucophane whereas all calcic amphiboles analyzedare barroisite-pargasite (Al2O3 greater than 10 wt. per cent). The garnet-epidote-rutile bearing glaucophane schist of Taiwanprobably recrystallized at temperatures above 350 ?C (the epidotezone) whereas the lawsonite-sphene glaucophane schists of theFranciscan equilibrated below 350 ?C (the lawsonite zone). TheMn-rich basaltic tuffs and their associated flows appear tohave been metamorphosed at profound depths and at the relativelyhigh temperatures of the epidote amphibolite facies, succeededlater by glaucophane schist facies metamorphism at lower temperatures. 相似文献
9.
The system peridotite-H2O–CO2 serves as a simplified modelfor the phase relations of mantle peridotite involving morethan one volatile component. Run products obtained in a studyof phase relations of four mantle peridotites in the presenceof H2O- and (H2O+CO2)- bearing vapors and with controlled hydrogenfugacity (fH2) at high pressures and temperatures have beensubjected to a detailed chemical investigation, principallyby the electron microprobe. Mg/(Mg+Fe) of all phases generally increases with increasingtemperature and with increasing Mg/(Mg+Fe) of the starting material.This ratio appears to decrease with increasing pressure forolivine, and for amphibole coexisting with garnet. DecreasingfH2 from that of IW buffer to that of MH buffer decreases Mg/(Mg+Fe)of the partial melt from approximately 0-85 to approximately0.50, whereas the Fo content of coexisting olivine increasesslightly less than 3 per cent and the Mg/(Mg+Fe) of clinopyroxeneincreases about 4 per cent. However, the variations in Fo contentof olivines are within those observed in olivines from naturalmantle peridotite. The chemistry of other silicate mineralsdoes not significantly reflect variations of fH2. Consequently,the peridotite mineralogy and/or chemistry is not a good indicatorfor the fH2 conditions during crystallization. All crystalline phases, except amphibole, and to some extentgarnet, show increasing Cr content with increasing temperatureand increasing Cr content of the starting material, resultingin a positive correlation with Mg/(Mg+Fe). Partial melts aredepleted in Cr2O3 relative to the crystalline phases. High Mg/Mg+Fe)and Cr2O3 are thus expected in crystal residues after partialmelting. The absolute values depend on degree of melting andthe composition of the parent peridotite. Liquids formed by anatexis of mantle peridotite are andesiticunder conditions of XH2Ov > 0.6 to at least 25 kb total pressureand to more than 200?C above the peridotite solidus. This observationsupports numerous suggestions that andesite genesis in islandarcs may result from partial melting of underlying peridotitemantle. In contrast to basaltic rocks, the absence of amphibole(paragasitic hornblende) does not affect the silica-saturatednature of the liquids. Increasing K2O content of the startingmaterial (up to 1 wt. per cent K2O) results in increasing potassiumcontent of the amphibole (1 wt. per cent K2O) as well as theappearance of phlogopite. The liquid under these conditionsis relatively K20-poor (less than 1 wt. per cent K2O). Partial melts are olivine normative with XH2O 0.5, and initialliquids contain normative ol and ne at XH2O 0.4. The alkalinityof these liquids increases with decreasing XH2O below valuesof 0.5. The (ol+opx)-normative liquids resemble oceanic basaltswhereas (ol+ne)-normative liquids resemble olivine nepheliniteand melilite basalt. Low aHlo and high aCo2 conditions may bethose under which kimberlites and related rocks are formed inthe mantle. 相似文献
10.
The magmatic processes leading to porphyry-Cu mineralizationat Santa Rita are reconstructed on the basis of petrographicstudies, thermobarometry, and laser-ablation inductively-coupled-plasmamass-spectrometry analyses of silicate melt and sulfide inclusionsfrom dikes ranging from basaltic andesite to rhyodacite. Combinedresults suggest that magma evolution at Santa Rita is similarto that of sulfur-rich volcanoes situated above subduction zones,being characterized by repeated injection of hot, mafic magmainto an anhydrite-bearing magma chamber of rhyodacitic composition.The most mafic end-member identified at Santa Rita is a shoshoniticbasaltic andesite that crystallized at 1000–1050°C,1–3 kbar and log fO2 = NNO + 0·7 to NNO + 1·0,whereas the rhyodacite crystallized at 730–760°C andlog fO2 = NNO + 1·3 to NNO + 1·9. Mixing betweenthe two magmas caused precipitation of 0·1–0·2wt % magmatic sulfides and an associated decrease in the Cucontent of the silicate melt from 300–500 ppm to lessthan 20 ppm. Quantitative modeling suggests that temporal storageof ore-metals in magmatic sulfides does not significantly enhancethe amount of copper ultimately available to ore-forming hydrothermalfluids. Magmatic sulfides are therefore not vital to the formationof porphyry-Cu deposits, unless a mechanism is required thatholds back ore-forming metals until late in the evolution ofthe volcanic–plutonic system. KEY WORDS: porphyry-Cu; sulfur; sulfides; magma mixing; LA-ICP-MS 相似文献
11.
Four natural peridotite nodules ranging from chemically depletedto Fe-rich, alkaline and calcic (SiO2=43?7–45?7 wt. percent, Al2O3=1?6O–8?21 wt. per cent, CaO=0?70–8?12wt. per cent,alk=0?10–0?90 wt. per cent and Mg/(Mg+Fe2+)=0?94–0?85)have been investigated in the hypersolidus region from 800?to 1250?C with variable activities of H2O, CO2, and H2. Thevapor-saturated peridotite solidi are 50–200?C below thosepreviously published. The temperature of the beginning of meltingof peridotite decreases markedly with decreasing Mg/(Mg+Fe)of the starting material at constant CaO/Al2O3. Conversely,lowering CaO/Al2O3 reduces the temperature at constant Mg/(Mg+Fe)of the starting material. Temperature differences between thesolidi up to 200?C are observed. All solidi display a temperatureminimum reflecting the appearance of garnet. This minimum shiftsto lower pressure with decreasing Mg/(Mg+Fe) of the startingmaterial. The temperature of the beginning of melting decreasesisobarically as approximately a linear function of the mol fractionof H2O in the vapor (XH2O). The data also show that some CO2may dissolve in silicate melts formed by partial melting ofperidotite. Amphibole (pargasitic hornblende) is a hypersolidus mineralin all compositions, although its P/T stability field dependson bulk rock chemistry. The upper pressure stability of amphiboleis marked by the appearance of garnet. The vapor-saturated (H2O) liquidus curve for one peridotiteis between 1250? and 1300?C between 10 and 30 kb. Olivine, spinel,and orthopyroxene are either liquidus phases or coexist immediatelybelow the temperature of the peridotite liquidus. The data suggest considerable mineralogical heterogeneity inthe oceanic upper mantle because the oceanic geotherm passesthrough the P/T band covering the appearance of garnet in variousperidotites. The variable depth to the low-velocity zone is explained byvariable aH2O conditions in the upper mantle and possibly alsoby variations in the composition of the peridotite itself. It is suggested that komatiite in Precambrian terrane couldform by direct melting of hydrous peridotite. Such melting requiresabout 1250?C compared with 1600?C which is required for drymelting. The genesis of kimberlite can be related to partial meltingof peridotite under conditions of (). Such activities of H2Oresult in melting at depths ranging between 125 and 175 km inthe mantle. This range is within the minimum depth generallyaccepted for the formation of kimberlite. 相似文献
12.
We present an experimental and petrological study aimed at estimatingthe pre-eruptive conditions of a Holocene dacitic lava fromVolcán San Pedro (36°S, Chilean Andes). Phase-equilibriumexperiments were performed at temperatures (T) from 800 to 950°C,and mainly at 200 MPa, but also at 55, 150, and 406 MPa. Oxygenfugacity (fO2) ranged from the Ni–NiO buffer (NNO) to3·5 log units above (NNO + 3·5), and water contentsfrom 相似文献
13.
The redox state of sillimanite zone (650–700°C, 5–6kbar) metasediments of the Barrovian type area, Scotland, wasinvestigated using estimates of metamorphic oxygen fugacity(fO2), sulfur fugacity (fS2), and fluid chemistry based on newdeterminations of mineral and rock compositions from 33 samples.A total of 94% of the samples lack graphite, contain both ilmenite–hematitesolid solutions (RHOMOX) and magnetite, and had metamorphicfO2 about 2 log10 units above the quartz–fayalite–magnetite(QFM) buffer. The regional variation in metamorphic fO2 forthese rocks was minimal, about ±0·3 log10 units,reflecting either a protolith that was homogeneous with respectto redox state, or an initially variable protolith whose redoxstate was homogenized by metamorphic fluid–rock interaction.RHOMOX inclusions in garnet porphyroblasts that become richerin ilmenite from the interior to the edge of the host porphyroblastsuggest that at least some syn-metamorphic reduction of rockoccurred. Significant variations in bulk-rock oxidation ratio(OR) that are probably inherited from sedimentary protolithsare found from one layer to the next; OR ranges mostly between 相似文献
14.
The melting relations of two proposed crustal source compositionsfor rhyolitic magmas of the Taupo Volcanic Zone (TVZ), New Zealand,have been studied in a piston-cylinder apparatus at 10 kb totalpressure and a range of water activities generated by H2O-CO2vapour. Starting materials were glasses of intermediate composition(65 wt.% Si02 representing a metaluminous ‘I-type’dacite and a peraluminous ‘S-type’ greywacke. Crystallizationexperiments were carried out over the temperature range 675to 975?C, with aH2O values of approximately 1?0, 0?75, 0?5,and 0?25. Talc-pyrex furnace assemblies imposed oxygen fugacitiesclose to quartz-fayalite-magnetite buffer conditions. Assemblages in both compositions remain saturated with quartzand plagioclase through 675–700?C at high aH2O, 725–750?Cat aH2O0?5, and 800–875?C at aH2O0?25, corresponding to<60–70% melting. Concentrations of refractory mineralcomponents (Fe, Mg, Mn, P, Ti) in liquids increase throughoutthis melting interval with increasing temperature and decreasingaH2O. Biotite and hornblende are the only mafic phases presentnear the solidus in the dacite, compared with biotite, garnet,gedritic orthoamphibole, and tschermakitic clinoamphibole inthe greywacke. Near-solidus melting reactions are of the type:biotite + quartz + plagioclase = amphibole ? garnet, potentiallyreleasing H2O for dehydration melting in the greywacke, butproducing larger amounts of hornblende and releasing littleH2O in the dacite. At aH2O0?25 and temperatures 825–850?C,amphibole dehydration produces anhydrous mineral phases typicalof granulite fades assemblages (clinopyroxene, orthopyroxene,plagioclase?quartz in the dacite; garnet, orthopyroxene, plagioclase?quartzin the greywacke) coexisting with melt proportions as low as40%. Hornblendce-saturated liquids in the dacite are weaklyperaluminous (0?3–1?6 wt.% normative C—within therange of peraluminous TVZ rhyolites), whereas, at aH2O0?25 andtemperatures 925?C, metaluminous partial melt compositions (upto 1?8 wt.% normative Di) coexist with plagioclase, orthopyroxene,and clinopyroxene. At all water activities, partial melts ofthe greywacke are uniformly more peraluminous (1?5–2?6wt.% normative C), reflecting their saturation in the componentsof more aluminous mafic minerals, particularly garnet and Al-richorthopyroxene. A metaluminous source for the predominantly Di-normativeTVZ rhyolites is therefore indicated. With decreasing aH2O the stability fields of plagioclase andquartz expand, whereas that of biotite contracts. These changesare reflected in the proportions of normative salic componentsin partial melts of both the dacite and greywacke. At high aH2O,partial melts are rich in An and Ab and poor in Or (trondhjemitic-tonalitic);with decreasing aH2O they become notably poorer in An and richerin Or (granodioritic-granitic). These systematic variationsin salic components observed in experimental metaluminous tostrongly peraluminous melts demonstrate that a wide varietyof granitoid magmas may be produced from similar source rocksdepending upon P-T-aH2O conditions attending partial melting.Some peraluminous granitoids, notably trondhjemitic leucosomesin migmatites, and sodic granodiorites and granites emplacedat deep crustal levels, have bulk compositions similar to nearsolidus melt compositions in both the dacite and greywacke,indicating possible derivation by anatexis without the involvementof a significant restite component. 相似文献
15.
Effect of Carbon Dioxide on Dehydration Melting Reactions and Melt Compositions in the Lower Crust and the Origin of Alkaline Rocks 总被引：9，自引：2，他引：7
Dehydration melting experiments of alkali basalt associatedwith the Kenya Rift were performed at 0·7 and 1·0GPa, 850–1100°C, 3–5 wt % H2O, and fO2 nearnickel–nickel oxide. Carbon dioxide [XCO2 = molar CO2/(H2O+ CO2) = 0·2–0·9] was added to experimentsat 1025 and 1050°C. Dehydration melting in the system alkalibasalt–H2O produces quartz- and corundum-normative trachyandesite(6–7·5 wt % total alkalis) at 1000 and 1025°Cby the incongruent melting of amphibole (pargasite–magnesiohastingsite).Dehydration melting in the system alkali basalt–H2O–CO2produces nepheline-normative tephriphonolite, trachyandesite,and trachyte (10·5–12 wt % total alkalis). In thelatter case, the solidus is raised relative to the hydrous system,less melt is produced, and the incongruent melting reactioninvolves kaersutite. The role of carbon dioxide in alkalinemagma genesis is well documented for mantle systems. This studyshows that carbon dioxide is also important to the petrogenesisof alkaline magmas at the lower pressures of crustal systems.Select suites of continental alkaline rocks, including thosecontaining phonolite, may be derived by low-pressure dehydrationmelting of an alkali basalt–carbon dioxide crustal system. KEY WORDS: alkali basalt; alkaline rocks; carbon dioxide; dehydration melting; phonolite 相似文献
16.
Experimental and Thermodynamic Constraints on the Sulphur Yield of Peralkaline and Metaluminous Silicic Flood Eruptions 总被引：1，自引：0，他引：1
Many basaltic flood provinces are characterized by the existenceof voluminous amounts of silicic magmas, yet the role of thesilicic component in sulphur emissions associated with trapactivity remains poorly known. We have performed experimentsand theoretical calculations to address this issue. The meltsulphur content and fluid/melt partitioning at saturation witheither sulphide or sulphate or both have been experimentallydetermined in three peralkaline rhyolites, which are a majorcomponent of some flood provinces. Experiments were performedat 150 MPa, 800–900°C, fO2 in the range NNO –2 to NNO + 3 and under water-rich conditions. The sulphur contentis strongly dependent on the peralkalinity of the melt, in additionto fO2, and reaches 1000 ppm at NNO + 1 in the most stronglyperalkaline composition at 800°C. At all values of fO2,peralkaline melts can carry 5–20 times more sulphur thantheir metaluminous equivalents. Mildly peralkaline compositionsshow little variation in fluid/melt sulphur partitioning withchanging fO2 (DS 270). In the most peralkaline melt, DS risessharply at fO2 > NNO + 1 to values of >500. The partitioncoefficient increases steadily for Sbulk between 1 and 6 wt% but remains about constant for Sbulk between 0·5 and1 wt %. At bulk sulphur contents lower than 4 wt %, a temperatureincrease from 800 to 900°C decreases DS by 10%. These results,along with (1) thermodynamic calculations on the behaviour ofsulphur during the crystallization of basalt and partial meltingof the crust and (2) recent experimental constraints on sulphursolubility in metaluminous rhyolites, show that basalt fractionationcan produce rhyolitic magmas having much more sulphur than rhyolitesderived from crustal anatexis. In particular, hot and dry metaluminoussilicic magmas produced by melting of dehydrated lower crustare virtually devoid of sulphur. In contrast, peralkaline rhyolitesformed by crystal fractionation of alkali basalt can concentrateup to 90% of the original sulphur content of the parental magmas,especially when the basalt is CO2-rich. On this basis, we estimatethe amounts of sulphur potentially released to the atmosphereby the silicic component of flood eruptive sequences. The peralkalineEthiopian and Deccan rhyolites could have produced 1017 and1018 g of S, respectively, which are comparable amounts to publishedestimates for the basaltic activity of each province. In contrast,despite similar erupted volumes, the metaluminous Paraná–Etendekasilicic eruptives could have injected only 4·6 x 1015g of S in the atmosphere. Peralkaline flood sequences may thushave greater environmental effects than those of metaluminousaffinity, in agreement with evidence available from mass extinctionsand oceanic anoxic events. KEY WORDS: silicic flood eruptions; sulphur; experiment; Ethiopia; Deccan 相似文献
17.
Experimental Petrology of the 1991-1995 Unzen Dacite, Japan. Part I: Phase Relations, Phase Composition and Pre-eruptive Conditions 总被引：2，自引：0，他引：2
HOLTZ FRANCOIS; SATO HIROAKI; LEWIS JARED; BEHRENS HARALD; NAKADA SETSUYA 《Journal of Petrology》2005,46(2):319-337
Crystallization experiments were conducted on dry glasses fromthe Unzen 1992 dacite at 100–300 MPa, 775–875°C,various water activities, and fO2 buffered by the Ni–NiObuffer. The compositions of the experimental products and naturalphases are used to constrain the temperature and water contentsof the low-temperature and high-temperature magmas prior tothe magma mixing event leading to the 1991–1995 eruption.A temperature of 1050 ± 75°C is determined for thehigh-temperature magma based on two-pyroxene thermometry. Theinvestigation of glass inclusions suggests that the water contentof the rhyolitic low-temperature magma could be as high as 8wt % H2O. The phase relations at 300 MPa and in the temperaturerange 870–900°C, which are conditions assumed to berepresentative of the main magma chamber after mixing, showthat the main phenocrysts (orthopyroxene, plagioclase, hornblende)coexist only at reduced water activity; the water content ofthe post-mixing dacitic melt is estimated to be 6 ± 1wt % H2O. Quartz and biotite, also present as phenocrysts inthe dacite, are observed only at low temperature (below 800–775°C).It is concluded that the erupted dacitic magma resulted fromthe mixing of c. 35 wt % of an almost aphyric pyroxene-bearingandesitic magma (1050 ± 75°C; 4 ± 1 wt % H2Oin the melt) with 65 wt % of a phenocryst-rich low-temperaturemagma (760–780°C) in which the melt phase was rhyolitic,containing up to 8 ± 1 wt % H2O. The proportions of rhyoliticmelt and phenocrysts in the low-temperature magma are estimatedto be 65% and 35%, respectively. It is emphasized that the strongvariations of phenocryst compositions, especially plagioclase,can be explained only if there were variations of temperatureand/or water activity (in time and/or space) in the low-temperaturemagma. KEY WORDS: Unzen volcano; magma mixing; experimental study 相似文献
18.
The Younger Andesites and Dacites of Iztacc?huatl volcano, Mexico,constitute a medium-K calcalkaline rock suite (58–66 wt.per cent SiO2) characterized by high Mg-numbers (100Mg/(Mg+0?85Fe2+=55–66) and relatively high abundances of MgO (2?5–6?6wt. per cent), Ni(17–158 p.p.m.), and Cr (42–224p.p.m.). Chemical stratigraphy plots of eruptive sequences indicatethe existence of a plexus of long-lived dacite magma chambersperiodically replenished by influxes of basaltic magma ascendingfrom depth. Short-term geochemical evolution after batch influxwas dictated by magma mixing and eventual dilution of the basalticcomponent by ‘quasi-steady state’ hornblende dacitemagma. The chemical data support textural and mineralogicalevidence for rapid homogenization of originally diverse magmasby convective blending of residual liquids accompanied by dynamicfractional crystallization (Nixon, 1988). Internally-consistent mixing calculations used to derive thecomposition of basaltic magma influx incorporate analyticaluncertainties and the observed range of salic end-member compositions.Mafic end-members are basalts to basaltic andesites (52–54wt. per cent SiO2) with Mg-numbers (73–76), MgO (9–11wt. per cent), Ni (250 p.p.m.), and Cr (340–510 p.p.m.)concentrations, and liquidus olivine compositions (Fo90–88),appropriate for unfractionated partial melts of mantle peridotite.The majority of model compositions are Ol-Hy-normative, similarto those of primitive basaltic lavas on the flanks of Iztacc?huatland in the Valley of Mexico. However, calculated magma batchesrange from weakly Qz-normative to strongly Ne-normative. Bothcalculated and analyzed basaltic compositions are distinguishedby highly variable abundances of alkalies and incompatible traceelements, notably Rb, Ba, Sr, P, Zr, and Y. Initial 87Sr/86Sr ratios for Iztacc?huatl lavas (0?7040–0?7046;n=24) are comparable to those for primitive basaltic rocks (0?7037–0?7045;?=4) and indicate that (1) mantle source regions are isotopicallyheterogeneous; and (2) contamination of iztacc?huatl magma chambersby radiogenic crustal rocks was not a significant factor inthe evolution of calc-alkaline andesites and dacites. The replenishment of Iztacc?huatl dacite reservoirs by Ne-normativemagmas late in the history of cone growth precludes exhaustionof mantle source regions by progressive partial melting. Thewaning stages of volcanic activity at Iztacc?huatl appear toreflect the inability of dense basaltic influxes to successfullypenetrate a large high-level chamber of low density hornblendedacite magma. 相似文献
19.
KADIK A.; PINEAU F.; LITVIN Y.; JENDRZEJEWSKI N.; MARTINEZ I.; JAVOY M. 《Journal of Petrology》2004,45(7):1297-1310
Studies of iron-bearing silicate melt (ferrobasalt) + iron metallicphase + graphite + hydrogen equilibria show that carbon andhydrogen solubilities in melts are important for the evolutionof the upper mantle. In a series of experiments conducted at3·7 GPa and 1520–1600°C, we have characterizedthe nature (oxidized vs reduced) and quantified the abundancesof C- and H-compounds dissolved in iron-bearing silicate melts.Experiments were carried out in an anvil-with-hole apparatuspermitting the achievement of equal chemical potentials of H2in the inner Pt capsule and outer furnace assembly. The fO2for silicate melt–iron equilibrium was 2·32 ±0·04 log units below iron–wüstite (IW). Theferrobasalt used as starting material experienced a reductionof its iron oxides and silicate network. The counterpart wasa liberation of oxygen reacting with the hydrogen entering thecapsule. The amount of H2O dissolved in the glasses was measuredby ion microprobe and by step-heating and was found to be between1 and 2 wt %. The dissolved carbon content was found to be 1600ppm C by step-heating. The speciation of C and H componentswas determined by IR and Raman spectroscopy. It was establishedthat the main part of the liberated oxygen was used to formOH– and to a much lesser extent H2O, and only traces ofH2, CO2 and 相似文献
20.
Ultra-calcic Magmas Generated from Ca-depleted Mantle: an Experimental Study on the Origin of Ankaramites 总被引：3，自引：1，他引：3
Ultra-calcic ankaramitic magmas or melt inclusions are ubiquitousin arc, ocean-island and mid-ocean ridge settings. They areprimitive in character (XMg > 0·65) and have highCaO contents (>14 wt %) and CaO/Al2O3 (>1·1). Experimentson an ankaramite from Epi, Vanuatu arc, demonstrate that itsliquidus surface has only clinopyroxene at pressures of 15 and20 kbar, with XCO2 in the volatile component from 0 to 0·86.The parental Epi ankaramite is thus not an unfractionated magma.However, forcing the ankaramite experimentally into saturationwith olivine, orthopyroxene and spinel results in more magnesian,ultra-calcic melts with CaO/Al2O3 of 1·21–1·58.The experimental melts are not extremely Ca-rich but high inCaO/Al2O3 and in MgO (up to 18.5 wt %), and would evolve tohigh-CaO melts through olivine fractionation. Fractionationmodels show that the Epi parent magma can be derived from suchultra-calcic experimental melts through mainly olivine fractionation.We show that the experimental ultra-calcic melts could formthrough low-degree melting of somewhat refractory mantle. Thelatter would have been depleted by previous melt extraction,which increases the CaO/Al2O3 in the residue as long as someclinopyroxene remains residual. This finding corrects the commonassumption that ultra-calcic magmas must come from a Ca-richpyroxenite-type source. The temperatures necessary for the generationof ultra-calcic magmas are 相似文献