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1.
The voluminous, bimodal, Silurian Topsails igneous suite consistsmainly of ‘A-type’ peralkaline to slightly peraluminous,hypersohnis to subsolvus granites with subordinate syenite,onzonite and diabase, plus consanguineous basalts and highsilicarhyolites. Nd(T) values from the suite range from –1.5to +5.4; most granitoid components exhibit positive Nd(T) values(+1.1 to +3.9). Granitoid initial 87Sr/86Sr and most 18 O valuesare in the range expected for rocks derived from mantle-likeprotoliths (0.701–0.706 and +6 to +80/). Restricted 207Pb/204Pbvariation is accompanied by significant dispersion of 206Pb/204Pband 208Pb/204Pb. Superficially, petrogenesis by either direct(via fractionation from basalt) or indirect (via melting ofjuvenile crust) derivation from mantle sources appears plausible.Remelting of the granulitic protolith of Ordovician are-typegranitoids can be ruled out, because these rocks exhibit negativeNd(T) and a large range in 207Pb/204Pb. Geochemical and isotopicrelationships are most compatible with remelting of hybridizedlithospheric mantle generated during arc-continent collision.A genetic link is suggested among collision-related delaminationor slab break-off events and emplacement of ‘post-erogenic’granite suites. A-type granites may recycle previously subductedcontinental material, and help explain the mass balance notedfor modern arcs. However, they need not represent net, new,crustal growth. KEY WORDS: A-type granites; juvenile crust; isotopes; Newfoundland *Telephone: (613) 995-4972. Fax: (613) 995-7997. e-mail: jwhalen{at}gsc.emr.ca  相似文献   

2.
The Ni-S System and Related Minerals   总被引：1，自引：0，他引：1  
The system Ni-S has been studied systematically from 200? to1, 030? C by means of evacuated, sealed silica-glass tube experimentsand differential thermal analyses. Compounds in the system areNi3S2 (and a high temperature, non-quenchable Ni3?S2 phase),Ni7S6, Ni1–S4 Ni3S4, and NiS2. The geologic occurrenceof the minerals heazlewoodite (Ni2S2), millerite (ßSNi1-2S),polydymite (Ni3S4), and vaesite (NiS2) can now be describedin terms of the stability ranges of their synthetic equivalents. Hexagonal heazlewoodite, which is stoichiometric within thelimit of error of the experiments, inverts on heating to a tetragonalor pseudotetragonal phase at 556? C. This high-temperature phase(Ni3 has a wide field of stability, from 23.5 to 30.5 wt percent sulfur at 600? C, and melts incongruently at 806??3? C.The ßNi7S6 phase inverts to Ni78 at 397? C6 when inequilibrium with Ni3S2, and at 400? C when in equilibrium withNiS. Crystals of Ni7S6 break down to Ni3-S2+NiS at 573??3?C.The low-temperature form of Ni1-S1 corresponding to the mineralmillerite, is rhombohedral, and the high-temperature form hasthe hexagonal NiAs structure. Stoichiometric NiS inverts at379??3?C, whereas Ni1-S with the maximum nickel deficiency invertsat 282??5OC. The Ni1-alphS-NiS2 solvus was determined to 985??3?C,the eutectic temperature of these phases. Stoichiometric NiSis stable at 600?C but breaks down to Ni2-S2 and Ni1-S below797?C, whereas Ni1-S with 38.2 wt per cent sulfur melts congruentlyat 992??3?C. Vaesite does not vary measurably from stoichiometricNiS2 composition, and melts congruently at 1.007?5?C. Polydymitebreaks down to aNi-S? vaesite at 356??3?C. Differential thermalanalyses showed the existence of a two-liquid field in the sulfur-richportion of the system above 991?C and over a wide compositionalrange.  相似文献   

3.
Geochemical and 40 Ar—39 Ar studies of the Malaita OlderSeries and Sigana Basalts, which form the basement of Malaitaand the northern portion of Santa Isabel, confirm the existenceof Ontong Java Plateau (OJP) crust on these islands. Sr, Nd,and Pb isotopic ratios of Malaita Older Series and Sigana lavasfall within limited ranges [(87Sr/86Sr)T= 0.70369–0.70423,ENd(T)= + 3.7 to +6.0, and 206Pb/204Pb = 18.25–18.64]virtually indistinguishable from those found in the three OJPbasement drill sites as far as 1600 km away, indicating a uniformhotspot-like mantle source with a slight ‘Dupal’signature for the world's largest oceanic plateau. Three chemicaltypes of basalts are recognized, two of which are equivalentto two of the three types drilled on the plateau, and one withno counterpart, as yet, on the plateau; the chemical data indicateslightly different, but all high, degrees of melting and slightvariation in source composition. All but one of the 40Ar-39Arplateau ages determined for Malaita Older Series and SiganaBasalt lavas are identical to those found at the distant drillsites: 121.30.9 Ma and 92.01.6 Ma, suggesting that two short-lived,volumetrically important plateau-building episodes took place30 m.y. apart. Aside from OJP lavas, three isotopically distinctsuites of alkalic rocks are present. The Sigana Alkalic Suitein Santa Isabel has an 40 Ar-39 Ar age of 91.70.4 Ma, the sameas that of the younger OJP tholeiites, yet it displays a distinct’HIMU‘ -type isotopic signature [206Pb/204Pb 20.20,(87Sr/86Sr) T 0.7032, Nd(T) 4.4], possibly representing small-degreemelts of a minor, less refractory component in the OJP mantlesource region. The Younger Series in southern Malaita has an40Ar-39Ar age of 44 Ma and isotopic ratios [Nd(T)=-0.5 to +1.0,(87Sr/86Sr)T =0.70404–0.70433, 206Pb/204Pb = 18.57–18.92]partly overlapping those of the ‘PHEM’ end-memberpostulated for Samoa, and those of present-day Rarotonga lavas;one or both of these hotspots may have caused alkalic volcanismon the plateau when it passed over them at 44 Ma. The NorthMalaita Alkalic Suite in northernmost Malaita is probably ofsimilar age, but has isotopic ratios [(87Sr/86Sr) T 0.7037,Nd(T) +4.5, 206pb/204pb 18.8) resembling those of some OJP basementlavas; it may result from a small amount of melting of agedplateau lithosphere during the OJP's passage over these hotspots.Juxtaposed against OJP crust in Santa Isabel is an 62–46-Maophiolitic (sensu lato) assemblage. Isotopic and chemical datareveal Pacific-MORB-like, backarc-basin-like, and arc-like signaturesfor these rocks, and suggest that most formed in an arc—backarcsetting before the Late Tertiary collision of the OJP againstthe old North Solomon Trench. The situation in Santa Isabelappears to provide a modern-day analog for some Precambriangreenstone belts. KEY WORDS: oceanic plateaux; Ontong Java Plateau; Solomon Islands; Sr-Nd-Pb isotopes; age and petrogenesis *Corresponding author.  相似文献   

4.
The Wrangellia terrane of North America contains a large volumeof Middle to Late Triassic oceanic flood basalts which wereemplaced on top of a preexisting island arc. Nd-, Sr-, and Pb-isotopiccompositions reflect derivation from a plume source with Nd(T)+6 to + 7, 87Sr/86Sri0•7034, and 206Pb/204Pbi19•0.Major and trace element compositions suggest the Wrangelliaflood basalts (WFB) formed through relatively small degreesof partial melting at greater depths than estimated for otheroceanic plateaux such as Ontong Java. It appears that the WFBdid not form in a rifting environment, and that preexistingarc lithosphere limited the ascent and decompression meltingof the source plume. Rocks from the preexisting arc are stronglydepleted in high field strength elements (HFSEs) relative tolarge ion lithophile elements (LILEs), but the WFB are not.Assimilation of arc lithospheric mantle or crust was thereforegenerally minor. However, some contamination by arc componentsis evident, particularly in basalts erupted in the early stagesof volcanism. Minor isotopic shifts, to lower Nd(T) and 206Pb/204Pbiand higher 87Sr/86Sri, are accompanied by shifts in trace elementratios towards more arclike signatures, e.g. low Nb/Th and Nb/La.Arc contamination is greatest in the most evolved basalts, indicatingthat assimilation was coupled with fractional crystallization.A comparison of the WFB with other continental and oceanic floodbasalts reveals that continental flood basalts generally formthrough smaller degrees of melting than oceanic flood basaltsand that the contribution of material from the crust and litho-sphericmantle is significantly greater. KEY WORDS: oceanic flood basalts; Wrangellia terrane; petrogenesis; Sr-Nd-Pb isotopes *Corroponding author  相似文献   

5.
The Jozini and Mbuluzi rhyolites and Oribi Beds of the southernLebombo Monocline, southeastern Africa, have geochemical characteristicsthat indicate they were derived by partial melting of a mixtureof high-Ti/Zr and low-Ti/Zr Sabie River Basalt Formation types.Compositional variations within the different rhyolite typescan largely be explained by subsequent fractional crystallization.The Sr- and Nd-isotope composition of the rhyolites is uniqueamongst Gondwana silicic large igneous provinces, having Ndvalues close to Bulk Earth (–0·94 to 0·35)and low, but more variable, initial 87Sr/86Sr ratios (0·7034–0·7080).Quartz phenocryst 18O values indicate that the rhyolite magmashad 18O values between 5·3 and 6·7, consistentwith derivation from a basaltic protolith with 18O values between4·8 and 6·2. The low-18O rhyolites (< 6·0)come from the same stratigraphic horizon and are overlain andunderlain by rhyolites with more ‘normal’ 18O magmavalues. These low-18O rhyolites cannot have been produced byfractional crystallization or partial melting of mantle-derivedbasaltic material. The rhyolites have low water contents, makingit unlikely that the low 18O values are the result of post-emplacementalteration. Modification of the source by fluid–rock interactionat elevated temperatures is the most plausible mechanism forlowering the 18O magma value. It is proposed that the low-18Orhyolites were derived by melting of earlier altered rhyolitein calderas situated to the east, which were not preserved afterGondwana break-up. KEY WORDS: rhyolite; Lebombo; stable and radiogenic isotopes; low-18O magmas; partial melting  相似文献   

6.
Alteration of a Komatiite Flow from Alexo, Ontario, Canada   总被引：5，自引：4，他引：1  
To investigate the ability of komatiites to preserve duringalteration a record of the geochemical and isotopic compositionof the Archean mantle, we studied the petrology and geochemistryof a komatiite flow from Alexo, Ontario. Although this flowis relatively well preserved, two main types of alteration arerecognized: (1) hydration of variable intensity throughout thewhole flow; (2) local rodingitization. In samples only slightlyaffected by hydration, the alteration was essentially isochemical;where more intense, hydration was accompanied by the mobilityof TiO2, Zr and the light rare-earth elements (LREE). The mobilityof these reputedly immobile trace elements is influenced bytexture and secondary mineral assemblages. Rodingitization wasaccompanied by still greater mobility. An Nd isochron with anage of 272698 Ma and Nd(T) =+ 2.5 is defined by wholerock samples.Because the spread of Sm-Nd ratios is far greater than can beexplained by magmatic processes, the age is interpreted as thatof the main alteration event during or soon after emplacement.Scattered initial Sr isotopic ratios and Nd (T) (+ 3.6 to +0.7)provide evidence for several younger events. The Nd (T) of magnaticclinopyroxene ( plus;3.8) is higher than that of mafic tofelsicrocks and pyroxenes from the Abibiti belt (Nd (T) +2.5). Thisresult implies: (1) the komatiites exchanged Nd with surroundingrocks during waterrock interaction; (2) the isotopic compositionof komatiites and their mantle source differed from that ofthe more common basalts of the Abitibi belt. KEY WORDS: alteration; Archean; Komatiite; trace elements; radiogenic and stable islotopes *Present address: Ore Genesis Research Group, VIEPS Department of Earth Science, Monash University, Clayton, Vic 3168, Australia. Telephone: (61) 3 9905-3881. Fax: (61) 3 9905–4903. e-mail: ylahaye{at}artemis.earth.monash.edu.au  相似文献   

7.
Klauea historical summit lavas have a wide range in matrix 18OVSMOWvalues (4·9–5·6) with lower values in rockserupted following a major summit collapse or eruptive hiatus.In contrast, 18O values for olivines in most of these lavasare nearly constant (5·1 ± 0·1). The disequilibriumbetween matrix and olivine 18O values in many samples indicatesthat the lower matrix values were acquired by the magma afterolivine growth, probably just before or during eruption. BothMauna Loa and Klauea basement rocks are the likely sources ofthe contamination, based on O, Pb and Sr isotope data. However,the extent of crustal contamination of Klauea historical magmasis probably minor (< 12%, depending on the assumed contaminant)and it is superimposed on a longer-term, cyclic geochemicalvariation that reflects source heterogeneity. Klauea's heterogeneoussource, which is well represented by the historical summit lavas,probably has magma 18O values within the normal mid-ocean ridgebasalt mantle range (5·4–5·8) based on thenew olivine 18O values. KEY WORDS: Hawaii; Klauea; basalt; oxygen isotopes; crustal contamination  相似文献   

8.
A suite of dolerite dykes from the Ahlmannryggen region of westernDronning Maud Land (Antarctica) forms part of the much moreextensive Karoo igneous province of southern Africa. The dykecompositions include both low- and high-Ti magma types, includingpicrites and ferropicrites. New 40Ar/39Ar age determinationsfor the Ahlmannryggen intrusions indicate two ages of emplacementat 178 and 190 Ma. Four geochemical groups of dykes have beenidentified in the Ahlmannryggen region based on analyses of60 dykes. The groups are defined on the basis of whole-rockTiO2 and Zr contents, and reinforced by rare earth element (REE),87Sr/86Sr and 143Nd/144Nd isotope data. Group 1 were intrudedat 190 Ma and have low TiO2 and Zr contents and a significantArchaean crustal component, but also evidence of hydrothermalalteration. Group 2 dykes were intruded at 178 Ma; they havelow to moderate TiO2 and Zr contents and are interpreted tobe the result of mixing of melts derived from an isotopicallydepleted source with small melt fractions of an enriched lithosphericmantle source. Group 3 dyke were intruded at 190 Ma and formthe most distinct magma group; these are largely picritic withsuperficially mid-ocean ridge basalt (MORB)-like chemistry (flatREE patterns, 87Sr/86Sri 0·7035, Ndi 9). However, theyhave very high TiO2 (4 wt %) and Zr (500 ppm) contents, whichis not consistent with melting of MORB-source mantle. The Group3 magmas are inferred to be derived by partial melting of astrongly depleted mantle source in the garnet stability field.This group includes several high Mg–Fe dykes (ferropicrites),which are interpreted as high-temperature melts. Some Group3 dykes also show evidence of contamination by continental crust.Group 4 dykes are low-K picrites intruded at 178 Ma; they havevery high TiO2–Zr contents and are the most enriched magmagroup of the Karoo–Antarctic province, with ocean-islandbasalt (OIB)-like chemistry. Dykes of Group 1 and Group 3 aresub-parallel (ENE–WSW) and both groups were emplaced at190 Ma in response to the same regional stress field, whichhad changed by 178 Ma, when Group 2 and Group 4 dykes were intrudedalong a dominantly NNE–SSW strike. KEY WORDS: flood basalt; depleted mantle; enriched mantle; Ahlmannryggen; Karoo dyke  相似文献   

9.
Hafnium isotope and incompatible trace element data are presentedfor a suite of mid-ocean ridge basalts (MORB) from 13 to 47°Eon the Southwest Indian Ridge (SWIR), one of the slowest spreadingand most isotopically heterogeneous mid-ocean ridges. Variationsin Nd–Hf isotope compositions and Lu/Hf ratios clearlydistinguish an Atlantic–Pacific-type MORB source, presentwest of 26°E, characterized by relatively low Hf valuesfor a given Nd relative to the regression line through all Nd–Hfisotope data for oceanic basalts (termed the ‘Nd–Hfmantle array line’; the deviation from this line is termedHf) and low Lu/Hf ratios, from an Indian Ocean-type MORB signature,present east of 32°E, characterized by relatively high Hfvalues and Lu/Hf ratios. Additionally, two localized, isotopicallyanomalous areas, at 13–15°E and 39–41°E,are characterized by distinctly low negative and high positiveHf values, respectively. The low Hf MORB from 13 to 15°Eappear to reflect contamination by HIMU-type mantle from thenearby Bouvet mantle plume, whereas the trace element and isotopiccompositions of MORB from 39 to 41°E are most consistentwith contamination by metasomatized Archean continental lithosphericmantle. Relatively small source-melt fractionation of Lu/Hfrelative to Sm/Nd, compared with MORB from faster-spreadingridges, argues against a significant role for garnet pyroxenitein the generation of most central SWIR MORB. Correlations betweenHf and Sr and Pb isotopic and trace element ratios clearly delineatea high-Hf ‘Indian Ocean mantle component’ that canexplain the isotope composition of most Indian Ocean MORB asmixtures between this component and a heterogeneous Atlantic–Pacific-typeMORB source. The Hf, Nd and Sr isotope compositions of IndianOcean MORB appear to be most consistent with the hypothesisthat this component represents fragments of subduction-modifiedlithospheric mantle beneath Proterozoic orogenic belts thatfoundered into the nascent Indian Ocean upper mantle duringthe Mesozoic breakup of Gondwana. KEY WORDS: mid-ocean ridge basalt; isotopes; incompatible elements; Indian Ocean  相似文献   

10.
Pliocene volcanics on the island of Bequia comprise two interbeddedsuites of basalts and andesites. The isotopically homogeneoussuite (IHS) has a limited range of Sr—Nd—Pb isotopes(87Sr/86Sr 0.7040–0.7046, 143 Nd/144 Nd 0.5130 and 206Pb/204Pb 19.36–19.51), and mantle-like 18O values (5.5in clinopyroxene). The isotopically diverse suite (IDS) is characterizedby much wider ranges of radiogenic isotopes (87 Sr/86Sr 0.7048–0.7077,143 Nd/144 Nd 0.5128–0.5123 and 206 Pb/204 Pb 19.7–20.2),in which all of the Sr and Pb ratios are higher and Nd ratiosare lower than those of the IHS. The IDS is also characterizedby high 18 O values, up to 7.6 in clinopyroxene. The Sr andPb isotope ratios are too high, and the Nd isotope ratios aretoo low in the IDS for any of these lavas to be derived fromunmodified depleted mantle. Both suites are petrologically very similar and their majorelement compositions and phenocryst contents suggest that theywere formed largely by fractional crystallization of a hydroustholeiitic melt at pressures <3 kbar. The isotopic ratiosand enrichments in large ion lithophile elements (LILE), andto some extent light rare earth elements (LREE), as comparedwith mid-ocean ridge basalts (MORB), of the IHS lavas suggestthat they were derived from a depleted mantle source which hadbeen re-enriched by the addition of 1–4% of a subductioncomponent. This component probably comprised a mixture of dehydrationfluids, and perhaps minor siliceous melts, released from subductingsediments and mafic crust. The extreme isotopic ranges, largeenrichments in incompatible elements, more fractionated LREEpatterns and higher 18 O values of the IDS lavas are interpretedas resulting from 10–55% assimilation—fractionalcrystallization of sediments, derived from the Guyana Shield,which are present in the arc crust, by IHS type melts. KEY WORDS: trace elements; radiogenic isotopes; arc lavas; Lesser Antilles *Corresponding author.  相似文献   

11.
Marbles and metapelites from the Reynolds Range Group (centralAustralia) were regionally metamorphosed at low pressure duringM2 at 1.6 Ga, M2 ranged in grade from greenschist to granulitefacies along the length of the Reynolds Range, and overprinted1.78 Ga granites and their contact aureoles in the ReynoldsRange Group metasediments. At all M2 grades the marbles andmetapelites have highly variable oxygen isotope ratios [marbles:18O(carb) 14–20%; metapelites: 18O 6–14%). Similarly, 1.78 Ga granites have highly variable oxygen isotope ratios(18O 5–13%), with the lowest values occurring at thegranite margins. In all rock types, the lowest oxygen isotopevalues are consistent with the infiltration of channelled magmaticand/or meteoric fluids. The variable lowering of oxygen isotopevalues resulted from pre-M2 contact metamorphism and fluid—rockinteraction around the 1.78 Ga granites. In contrast, mineralassemblages in the marbles define a trend of increasing XCO2with increasing grade from <0.05 (greenschist facies) to0.7–1.0 (granulite facies). This, together with the lackof regionally systematic resetting of oxygen isotope ratios,implies that there was little fluid—rock interaction duringprograde regional metamorphism. KEY WORDS: low pressure; polymetamorphism; fluids; stable isotopes; petrology *Corresponding author Fax: 61–3–94791272. e-mail: geoisb{at}lure.latrobe.edu.au  相似文献   

12.
A new method has been suggested for evaluating the overall basicityof minerals and rocks by using ionization reactions involvingone proton: (sum of cations) + H2O = mineral + H+, (sum of cations) + H2O = (sum of normative minerals of a rock)+ H+. The basicity indicators are expressed as standard free energychanges of these reactions (). At standard water pressure (logPH2O = 0) and chemical activity of the metal ions ( log Mn+= 0), the relationship between and alkalinity of solutions(pH) becomes: = –2.303 RTlog H+ = 2.303 RT pH. The overall basicities of rock-forming oxides, minerals andmajor rocks were calculated from the thermodynamic data on ionsin water solutions and solid compounds.  相似文献   

13.
An oxygen and hydrogen isotopic study of minerals and wholerocks from the granites of the Mourne Mountains Tertiary complex,and related rocks, shows that whereas a significant circulationof meteoric water was associated with the complex, it had onlyminor and localized effects on the granites themselves. TheSilurian slate and greywacke country rocks, which would havehad 18O(SMOW) values of +10 to +20 before the Tertiary igneousevents, have been depicted 18O to values of –40 to –05Tertiary acid minor intrusions outside the main granite massesare also 18O depleted. l8O whole-rock data on the granites showa range of +6.0 to +9.5, and include values significantly higherthan most of those obtained for the granites of the Tertiarycentral complexes of Skye, Mull, and Ardnamurchan. Many of thelowest whole-rock 18O values are found in samples where theminerals are not in isotopic equilibrium. The mineral oxygenisotopic data can be explained in terms of localized interactionwith meteoric water, resulting in preferential 18O depletionin feldspar(s) and biotite, with quartz being much less affected.The granites all show low values of D(SMOW) for biotite andamphibole separates (–137 to –104). The lowest valuesoccur close to the margins of the plutons, near internal contactsor near greisen localities, and these probably reflect limitedinteraction with meteoric water. The higher D values are fromsamples which show evidence of chloritization. This processappears to have occurred both during interaction with meteoricwater, and also during autometasomatism by an exsolved magmaticfluid in other parts of the plutons, including central locationswhere there is little or no evidence for the penetration ofmeteoric water. Granite samples which exhibit near-equilibriumoxygen isotope fractionations for constituent minerals are characterizedby magmatic O-isotopic compositions. The G2 granite, the largestpluton of the eastern centre, has a magmatic 18O(SMOW) valueof {small tilde}+95; intrusions G3 (eastern centre) and G4(western centre) both have 18O(SMOW) values of {small tilde}+90.The other two main intrusive phases have distinctly lower 18O(SMOW)values: {small tilde}+75 for Gl (the least fractionated graniteof the Mourne Mountains central complex), and from +75 to +85for G5. The oxygen isotopic data rule out simple partial meltingof the country rocks as the origin of the granites and alsopreclude an origin by closed-system fractional crystallizationof basaltic magma typical of that represented by Tertiary basicigneous rocks of the region. * Present address: NERC Isotope Geosciences Laboratory, Keyworth, Nottingham BG12 5GG, UK Present address: School of Engineering Technology, Georgian College, Barrie, Ontario, L4M 3X9, Canada  相似文献   

14.
Pan-African high-grade metamorphism in the Kerala KhondaliteBelt (South India) led to the in situ formation of garnet-bearingleucosomes (L1) in sodic quartz—alkali feldspar—biotitegneisses. Microtextures, mineralogy and the geochemical characteristicsof in situ leucosomes (L1) and gneiss domains (GnD) indicatethat the development of leucosomes was mainly controlled bythe growth of garnet at the expense of biotite. This is documentedby the selective transfer of FeO, MgO, , Sm and the heavy rareearth elements into the L1 domains. P-T constraints (T>800C,P>6kbar, aH2O0.3) suggest that the leucosomes were formedthrough complete melting of biotite in fluid-absent conditions,following the model reaction Biotite+Alkali feldspar+QuartzlGarnet+Ilmenite+Melt.The fraction of melt generated during this process was low (<10vol.%). The identical size of the leucosomes as well as theirhomogeneous and isotropic distribution at outcrop scale, whichlacks any evidence for melt segregation, suggest that the migmatiteremained a closed system. Subsequent to migmatization, the leptyniticgneisses were intruded by garnet-bearing leucogranitic melts(L2), forming veins parallel and subperpendicular to the foliation.The leucogranites are rich in potassium (K2O5.5 wt%), (Ba400p.p.m.) and Sr (300 p.p.m.), and exhibit low concentrationsof Zr (40 p.p.m.), Th (<1 p.p.m.) and (<10 p.p.m.). Thechondrite-normalized REE spectra show low abundances (LaN20,LuN3) and are moderately fractionated (LaN/LuN7). An Eu anomalyis absent or weakly negative. The higher 87Sr/86Sr ratio at550 Ma (0.7345) compared with the migmatite (0.7164) precludesa direct genetic relationship between leptynitic gneisses andleucogranites at Manali.Nevertheless, the chemical and mineralogicalcompositions of the leuocogranites strongly favour a derivationthrough fluid-absent biotite melting of isotopically distinctbut chemically comparable Manali-type gneisses. The undersaturationof Zr, Th and REE, a typical feature of leucogranitic meltsgenerated during granulite facies anatexis of psammo-peliticlithologies and attributed to disequilibrium melting with incompletedissolution of accessory phases (zircon, monazite), is weaklydeveloped in the leucogranites of Manali.It is concluded thatthis is mainly due to the sluggish migration of the melts instatic conditions, which facilitated equilibration with therestitic gneisses. *Fax: 0228-732763; e-mail: ingo.braun{at}uni-bonn.de  相似文献   

15.
Mount Galunggung is a historically active volcano in southwesternJava that has erupted four times in the last two centuries.During the most recent event, which occurred during a 9–monthinterval in 1982– 83, some 305 106 m3 of medium–K,calc–alkaline magma was erupted. This eruption was unusualbecause of its duration, the diversity of eruption dynamicsand products, and the range of lava compositions produced. Thecomposition of juvenile material changed gradually during thecourse of the eruption from initial plagioclase (An60–75)and two–pyrozene bearing andesites with 58% SiO2 to finalplagioclase (An85–90), diopside, and olivine (Fo85–90)bearing primitive magnesium basalts with 47% SiO2 Mineralogicaland compositional relationships indicate a magmatic evolutioninvolving differentitation of high–Mg parental melt. Theeruptive volumes of 35 106 m3 andesite, 120 106 m3 maficandesite, and 150 106 m3 basalt are consistent with the ideathat the 1982– 83 eruption progressively tapped and draineda magma chamber that had become chemically stratified throughextensive crystal fractionation. Separates of plagioclase and pyroxene have 18O( SMO W) rangesof + 5. 6 to + 6.0 and + 5.3 to + 5.6, respectively, with 18Oplag–pxvalues of + 0.4 to + 0.6o, indicating internal O–isotopeequiliburium at temperature of 1100–850 C. The magenesianbasalts have magmatic 18O/ 16O ratios similar to those of mid–oceanridge basalt, and the O–isotope ratios of compositionallyevolved derivative melts show no evidence for contaminationof the galunggung magmas by 18O–rich crust during differentiation.Andesites and transitional mafic and sites have a more variableO–isotope character, with laves and phenocrysts havingboth higher and lower 18O values than observed in the parentalmagnesium basalts. These features are interpreted to reflectintramagma chamber processes affecting the upper portions ofthe differentiating Galunggung magma body before the 1982–83eruption.  相似文献   

16.
BAKER  A. J. 《Journal of Petrology》1990,31(1):243-260
Stable isotope compositions of Ivrea Zone marbles and associatedlithologies are in general heterogeneous. The oxygen isotopecomposition of quartz in pelites ranges from 18O +9 to + 17(SMOW) and does not vary systematically with metamorphic grade.Peridotites retain oxygen isotope signatures close to mantlevalues. Marble calcites vary in isotopic composition from 13C + 2(PDB),180 +24(SMOW)to 13C –6(PDB), 18O + 13 (SMOW).Depletions in 18O and 13C may be explained dominantly by interactionwith fluids derived from within the observed metasedimentarysequence during prograde metamorphism. 18O and 13C show gradients of greater than 5/m across marblemargins and within marbles. The preservation of such isotopicgradients is not consistent with the long-term presence of grain-boundary-scaleinterconnected fluid films in and around marbles. There is ageneral lowering of 18O within individual marble bodies althoughlarge carbon and oxygen isotopic gradients are present. Calcitein marbles may attain oxygen isotope equilibrium, but rarelycarbon isotope equilibrium, with surrounding metapelites. Infiltrationof marbles must involve a component of channelized fluid flow. The general lack of isotopic equilibration within the sequencerequires channelized fluid flow and limited fluid-rock ratios.Large pervasive mantle to crust fluid fluxes are not consistentwith the observations. *Present address: Natural Environment Research Council, Polaris House, North Star Avenue, Swindon SN2 1EU, England  相似文献   

17.
This study reports oxygen isotope ratios determined by laserfluorination of mineral separates (mainly plagioclase) frombasaltic andesitic to rhyolitic composition volcanic rocks eruptedfrom the Lassen Volcanic Center (LVC), northern California.Plagioclase separates from nearly all rocks have 18O values(6·1–8·4) higher than expected for productionof the magmas by partial melting of little evolved basalticlavas erupted in the arc front and back-arc regions of the southernmostCascades during the late Cenozoic. Most LVC magmas must thereforecontain high 18O crustal material. In this regard, the 18O valuesof the volcanic rocks show strong spatial patterns, particularlyfor young rhyodacitic rocks that best represent unmodified partialmelts of the continental crust. Rhyodacitic magmas erupted fromvents located within 3·5 km of the inferred center ofthe LVC have consistently lower 18O values (average 6·3± 0·1) at given SiO2 contents relative to rockserupted from distal vents (>7·0 km; average 7·1± 0.1). Further, magmas erupted from vents situated attransitional distances have intermediate values and span a largerrange (average 6·8 ± 0·2). Basaltic andesiticto andesitic composition rocks show similar spatial variations,although as a group the 18O values of these rocks are more variableand extend to higher values than the rhyodacitic rocks. Thesefeatures are interpreted to reflect assimilation of heterogeneouslower continental crust by mafic magmas, followed by mixingor mingling with silicic magmas formed by partial melting ofinitially high 18O continental crust (9·0) increasinglyhybridized by lower 18O (6·0) mantle-derived basalticmagmas toward the center of the system. Mixing calculationsusing estimated endmember source 18O values imply that LVC magmascontain on a molar oxygen basis approximately 42 to 4% isotopicallyheavy continental crust, with proportions declining in a broadlyregular fashion toward the center of the LVC. Conversely, the18O values of the rhyodacitic rocks suggest that the continentalcrust in the melt generation zones beneath the LVC has beensubstantially modified by intrusion of mantle-derived basalticmagmas, with the degree of hybridization ranging on a molaroxygen basis from approximately 60% at distances up to 12 kmfrom the center of the system to 97% directly beneath the focusregion. These results demonstrate on a relatively small scalethe strong influence that intrusion of mantle-derived maficmagmas can have on modifying the composition of pre-existingcontinental crust in regions of melt production. Given thisresult, similar, but larger-scale, regional trends in magmacompositions may reflect an analogous but more extensive processwherein the continental crust becomes progressively hybridizedbeneath frontal arc localities as a result of protracted intrusionof subduction-related basaltic magmas. KEY WORDS: oxygen isotopes; phenocrysts; continental arc magmatism; Cascades; Lassen  相似文献   

18.
Progress () of the infiltration-driven reaction, 4olivine +5CO2 + H2O = talc + 5magnesite, that occurred during Barrovianregional metamorphism, varies at the cm-scale by a factor of3·5 within an 3 m3 volume of rock. Mineral and stableisotope compositions record that XCO2, 18Ofluid, and 13Cfluidwere uniform within error of measurement in the same rock volume.The conventional interpretation of small-scale variations in in terms of channelized fluid flow cannot explain the uniformityin fluid composition. Small-scale variations in resulted insteadbecause (a) reactant olivine was a solid solution, (b) initiallythere were small-scale variations in the amount and compositionof olivine, and (c) fluid composition was completely homogenizedover the same scale by diffusion–dispersion during infiltrationand subsequent reaction. Assuming isochemical reaction, spatialvariations in image variations in the (Mg + Fe)/Si of the parentrock rather than the geometry of metamorphic fluid flow. Ifinfiltration-driven reactions involve minerals fixed in composition,on the other hand, spatial variations in do directly imagefluid flow paths. The geometry of fluid flow can never be determinedfrom geochemical tracers over a distance smaller than the oneover which fluid composition is completely homogenized by diffusion–dispersion. KEY WORDS: Alpine Barrovian metamorphism; diffusion; metamorphic fluid composition; metamorphic fluid flow; reaction progress  相似文献   

19.
New Rb-Sr and trace element data are reported for the GreatDyke and Bushveld Mafic Phase layered intrusions. It is arguedthat geochemical characteristics, such as 87Sr/86Sr ratios andR.E.E. distribution patterns have been little modified by crustalcontamination. Rb-Sr data for whole-rocks of the Great Dyke yield an age of2514±16 m.y. and an initial 87Sr/86Sr ratio of 0.70261±4.Mineral data are consistent with these results. The low errorson the results indicate no significant variation of 87Sr/86Srratios of successive magmatic influxes emplaced in differentmagma chambers. Earlier Great Dyke magmas were highly Mg-richand represent extensive partial melts of the source material.One such influx is shown to have a high Rb/Sr ratio (0.25) anda fractionated R.E.E. pattern (CeN/YBN 12). These ratios areconsidered to approximate those of the source region. The Bushveld Mafic Phase has been dated accurately for the firsttime and has a Rb-Sr age of 2095±24 m.y. Initial 87Sr/86Srratios increase in a stepwise manner upwards in the intrusionfrom 0.70563±2 to 0.70769±6. Each increase isabrupt and occurs at a horizon also characterized by a suddenirregularity in cryptic variation. The Mafic Phase was emplacedas a succession of magmatic influxes each of which had higher87Sr/86Sr ratio than its predecessor. The first magma was both Mg-rich (MgO 21.5 per cent) and SiO2-rich(50–55 per cent SiO2) and was derived by extensive partialmelting of a shallow level upper mantle source. This sourcewas characterized by trace element abundance ratios (e.g. Rb/Sr 0.25; K/Rb 90; CeN/YbN 11), similar to those of kimberlitesand some potassic lavas and comparable with those deduced forthe Great Dyke source region. It is postulated that when the Rhodesian and Kaapvaal cratonsstabilized, underlying refractory mantle became fixed theretoto form a proto-lithosphere. Shortly afterwards, at about 2800m.y. ago, this proto-lithospheric mantle was enriched by passagethrough it of fluids with kimberlitic trace element chemistry.This sub-cratonic mantle thereafter evolved with a relativelyhigh Rb/Sr ratio. Magmas derived from it have anomalous chemicalcharacteristics with respect to those of ocean-floor basalts,reflecting major differences in the evolution of their respectivesource regions.  相似文献   

20.
Quaternary lavas and pyroclastic rocks of Mount Mazama, CraterLake caldera, and the surrounding area have variable Sr, Nd,and Pb isotopic compositions. High-alumina olivine tholeiites(HAOT) have 87Sr/86Sr ratios of 0.70346–0.70364; basalticandesite, 0–70349–0.70372; shoshonitic basalticandesite, 0.70374–0.70388; and andesite, 0.70324–0.70383.Dacites of Mount Mazama have 87Sr/86Sr ratios of 0.70348–0.70373.Most rhyodacites converge on 0.7037. However, rhyodacite ofthe caldera-forming, climactic eruption has 87Sr/86Sr=0.70354because of an admixed low-87Sr/86Sr component. Andesitic tomafic-cumulate scoriae of the climactic eruption, and enclavesin preclimactic rhyodacites, cluster in two groups but shownearly the entire 87Sr/86Sr range of the data set, confirmingpreviously suggested introduction of diverse parental magmasinto the growing climactic chamber. Pb and Nd isotope ratiosdisplay less variation (206Pb/204Pb= 18.838–18.967, 207Pb/204Pb=15.556–15.616,208Pb/204Pb=38.405–38.619; Nd= +3.9 to +6.1) and generallycovary with 87Sr/86 Sr ratios. Radiogenic isotope data fromCrater Lake plot with published data for other Cascade volcanoeson isotope ratio correlation diagrams. The isotopic data for the Crater Lake area require sources ofprimitive magmas to consist of depleted mantle and a subductioncomponent, introduced in variable quantity to the depleted mantlewedge. Variable degrees of melting of this heterogeneous mantle,possibly at different depths, produced the diversity of isotopiccompositions and large-ion lithophile element (LILE) abundancesin primitive magmas. Trace element ratios do not indicate presenceof an ocean island basalt (OIB) source component that has beenreported in lavas of some other Cascade volcanoes. Crustal contamination may have affected isotope ratios and LILEconcentrations in evolved HAOT, where initial LILE concentrationswere low. Contamination is more difficult to detect in the calcalkalinelavas because of their higher LILE concentrations and the smallisotopic contrast with likely contaminants, such as mid- tolower-crustal rocks thought to be equivalents of igneous rocksof the Klamath Mountains and associated lower crust. Crustalassimilation appears to be required for calcalkaline rocks onlyby 18O values, which vary from lows of +5.6 to + 6.0% in HAOTand primitive basaltic andesites to a high of +7.0% in dacite,a range that is too high to be explained by plagioclase-dominatedclosed-system fractional crystallization. Elevated 18O valuesof differentiated lavas may be attributed to interaction withrelatively 18O-rich, 87Sr-poor crustal rocks. Variably fused granitoid blocks ejected in the climactic eruption,and rarely in late Pleistocene eruptive units, have 18Opl of–3.4 to +6.5% and 18Oqz of –2.2 to +8.0% but haveSr, Nd, and Pb isotope ratios similar to volcanic rocks (e.g.87Sr/86Sr0.7037). Rb and Sr data for glass separates from granodioritessuggest that the source pluton is Miocene. Glass from granodioritehas 87Sr/86Sr ratios as high as 0.70617. Oxygen isotope fractionationbetween quartz, plagioclase, and glass indicates requilibrationof O isotopes at magmatic temperatures, after 18O/16O had beenlowered by exchange with meteoric hydrothermal fluids. Unmeltedgranodiorite xenoliths from pre-climactic eruptive units have18O values that are consistent with onset of hydrothermal exchangeearly during growth of the climactic magma chamber. Assimilationof such upper-crustal granodiorite apparently lowered 18O valuesof rhyodacites without significantly affecting their magmaticcompositions in other ways.  相似文献   

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