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1.
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   

2.
The present work reports the first broad geochemical investigationof the recently discovered late Archean (2700 Ma) Skjoldungenalkaline igneous province (SAP) in southeast Greenland. Therocks studied range in composition from ultramafic to felsicand comprise pyroxenites, hornblendites, hornblende noritesand diorites, monzonites, syenites, and nephelinitic rocks andcarbonatites. Various lithologic units from the host Archeangneissic basement are also investigated. The magmatic rocksshow remarkably coherent major element, trace element, rareearth element (REE), and Sr and Nd isotope systematics, suggestinga petrogenetic relationship. The most important geochemicalfeatures are high normative proportions of nepheline, forsteriteand albite, low TiO2 (<15 wt %) and moderate FeO (total)(<12 wt %) contents, enrichments in large ion lithophileelements (LILE) and light rare earth elements both absoluteand relative to high field strength elements (HFSE) that displaylarge negative anomalies, and generally low to moderate abundancesof compatible elements. Field relations and REE and compatibleelement systematics among Skjoldungen rocks suggest that maficand ultramafic hornblende-rich samples may represent cumulatelithologies of the regional parental magma. On the basis ofmineral data, this is deduced to have had mg-number of 064,shoshonitic affinities (K2O15 wt %), been close to silica saturationand volatile rich. Major element, trace element and REE systematicsfurther suggest that felsic intrusions are related to the maficregional parental magma through extensive olivine, hyperstheneand hornblende fractionation. Lack of correlation between La/Yband other critical trace and REE ratios indicates that apatite,zircon and titaniferous minerals were not important cumulusphases at advanced stages of evolution. The measured Sm–Ndwhole-rock isochron age is 2716 23 Ma (2 error) [mean squareof weighted deviates (MSWD) = 14], whereas linear regressionof the Sr isotope data yields an age of 26047 Ma (2 error)(MSWD = 22•2). The age obtained by Nd isotopes is corroboratedby U–Pb zircon results (2698 7 Ma), suggesting thatthe Sm–Nd system remained closed since crystallization.By contrast, the 100 Ma younger age obtained by Sr isotopessuggests that the Rb–Sr system has been disturbed. Initial143Nd/144 Nd ratios span a narrow range corresponding to Nd(27Ga) =+074 to –109, whereas initial Sr values at 27Ga cover a comparatively larger interval from –10 to +20.Neither initial Nd nor initial Sr values conform to previouslysuggested mantle depletion curves and no meaningful correlationexists between Nd and Sr isotopes for the Skjoldungen magmaticrocks as a whole. Although compositionally heterogeneous, theanalyzed suite of samples from the host agmatitic basement isextremely homogeneous with respect to age, with TCHUR crustalresidence times around 2700–2800 Ma confirming limitedavailable isotopic evidence. Large-scale assimilation of Archeancrust or recycling of sediments derived from the local basementinto the mantle source fails to explain adequately negativeNb anomalies and low Nd signatures characteristic of the Skjoldungenintrusions. Rather, the nearchondritic isotopic compositionof Nd in the Skjoldungen samples together with the decoupledLILE and HFSE enrichment and slightly positive Sr values areconsidered to reflect characteristics of the mantle source ina subduction zone environment. The geodynamic site hosting theSkjoldungen province thus may be an early manifestation of modern-styleplate tectonics. KEY WORDS: Skjoldungen province; Greenland; Archean; alkaline igneous rocks; geochronology; geochemistry *Corresponding author. Present address: Ecole Normale Suprieure de Lyon, 46 AlLe d'Italie, 69364 Lyon Cedex 07, France  相似文献   

3.
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   

4.
A Stable Isotope Study of Anorogenic Magmatism in East Central Asia   总被引：8，自引：0，他引：8  
A stable isotope study of 168 plutonic igneous rock and fivewater samples from Transbaikalia, East Asia, has been made,including 318 whole-rock and mineral 18O/16O analyses and 14D/H analyses. This represents the first detailed isotopic studyof the enormous Phanerozoic K-rich (mostly anorogenic) granitoidbelts of this region, which are thousands of kilometers in lengthand span an age range of >250Ma. Of the five main intrusivesuites, emplacement of the youngest (Permo-Triassic) was accompaniedby intense meteoric-hydrothermal activity, locally causing extreme18O depletio (18O feldspar<–12). This reflects thevery low 18O of the water involved in these systems, which probablyhad 18O < – 20 and D < – 150, consistent withthe high paleolatitude of Transbaikalia in the early Mesozoic(80N). Despite local post-emplacement, hydrothermal 18O-depletioneffects near Permo-Triassic and younger plutons, the variationof magmatic isotopic composition in the five intrusive suites,in space and time, can be clearly discerned using the 18O/16Ovariation in phases such as quartz and sphene that are resistantto sub-solidus exchange. A procedure for analyzing 18O/16O insphene using a laser fluorination technique is described: analysisof samples as small as 0.4 mg (including single crystals ofsphene from granitoids) is possible and provides an effectiveway to estimate the magmatic 18O value of plutonic igneous rocks.Most sphene and quartz 18O values vary by 1.0–2.0% withineach of the five main intrusive suites in Transbaikalia (rangingin age from mid-Paleozoic to Mesozoic), and are uniform bothwithin individual plutons and among plutons of the same suiteseparated by tens or hundreds of kilometers. However, each suitehas a unique range in 18O/16O, indicating that, on a regionalscale, the magmatic 18O values of these granitoids decreasedprogressively in 1% decrements from +10 in the earliest groupto +6 in the youngest. This progression was accompanied by increasesin the concentration of elements such as K and Zr, and decreasesin the concentration of elements such as Sr and Ba. These systematicsrequire large scale deep crustal melting and mixing processesto generate the compositional uniformity of individual plutonsand groups over such wide areas, and also a progressive hybridizationof the crust with alkalic, mantle-derived magmas to generatesyenites and granites with progressively lower 18O values. Thisprocess may be a hallmark of anorogenic granitoid petrogenesisand the intracontinental cratonization process in general, andalso represents an important (though largely cryptic) crustalgrowth mechanism. KEY WORDS: anorogenic granitoids; crustal growth; hybridization; hydrothermal systems; stable isotopes 1Present address: Galson Sciences Limited, 5 Grosvenor House, Melton Road, Oakham LE15 6AX, UK.  相似文献   

5.
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   

6.
Tourmaline in the Martinamor antiform occurs in tourmalinites(rocks with >15–20% tourmaline by volume), clasticmetasedimentary rocks of the Upper Proterozoic Monterrubio formation,quartz veins, pre-Variscan orthogneisses and Variscan graniticrocks. Petrographic observations, back-scattered electron (BSE)images, and microprobe data document a multistaged developmentof tourmaline. Overall, variations in the Mg/(Mg + Fe) ratiosdecrease from tourmalinites (0·36–0·75),through veins (0·38–0·66) to granitic rocks(0·23–0·46), whereas Al increases in thesame order from 5·84–6·65 to 6·22–6·88apfu. The incorporation of Al into tourmaline is consistentwith combinations of xAl(NaR)–1 and AlO(R(OH))–1exchange vectors, where x represents X-site vacancy and R is(Mg + Fe2+ + Mn). Variations in x/(x + Na) ratios are similarin all the types of tourmaline occurrences, from 0·10to 0·53, with low Ca-contents (mostly <0·10apfu). Based on field and textural criteria, two groups of tourmaline-richrocks are distinguished: (1) pre-Variscan tourmalinites (probablyCadomian), affected by both deformation and regional metamorphismduring the Variscan orogeny; (2) tourmalinites related to thesynkinematic granitic complex of Martinamor. Textural and geochemicaldata are consistent with a psammopelitic parentage for the protolithof the tourmalinites. Boron isotope analyses of tourmaline havea total range of 11B values from –15·6 to 6·8;the lowest corresponding to granitic tourmalines (–15·6to –11·7) and the highest to veins (1·9to 6·8). Tourmalines from tourmalinites have intermediate11B values of –8·0 to +2·0. The observedvariations in 11B support an important crustal recycling ofboron in the Martinamor area, in which pre-Variscan tourmaliniteswere remobilized by a combination of mechanical and chemicalprocesses during Variscan deformation, metamorphism and anatexis,leading to the formation of multiple tourmaline-bearing veinsand a new stage of boron metasomatism. KEY WORDS: tourmalinites; metamorphic and granitic rocks; mineral chemistry; whole-rock chemistry; boron isotopes  相似文献   

7.
A combination of major and trace element, whole-rock Sr, Ndand Hf isotope, and zircon U–Pb isotopic data are reportedfor a suite of dolerite dikes from the Liaodong Peninsula inthe northeastern North China Craton. The study aimed to investigatethe source, petrogenesis and tectonic setting of the dikes.Sensitive high-resolution ion microprobe U–Pb zircon analysesyield a Late Triassic emplacement age of 213 Ma for these dikes,post-dating the collision between the North China and Yangtzecratons and consequent ultrahigh-pressure metamorphism. Threegeochemical groups of dikes have been identified in the LiaodongPeninsula based on their geochemical and Sr–Nd–Hfisotope characteristics. Group 1 dikes are tholeiitic, withhigh TiO2 and total Fe2O3 and low MgO contents, absent to weaknegative Nb and Ta anomalies, variable (87Sr/86Sr)i (0·7060–0·7153),Nd(t) (– 0·8 to –6·5) and Hf(t) (–2·7to –7·8) values, and negative Hf(t) (–1·1to –7·8). They are inferred to be derived frompartial melting of a relatively fertile asthenospheric mantlein the spinel stability field, with some upper crustal assimilationand fractional crystallization. Group 2 dikes have geochemicalfeatures of high-Mg andesites with (87Sr/86Sr)i values of 0·7063–0·7072,and negative Nd(t) (–3·0 to –9·5)and Hf(t) (–3·2 to –10·1) values,and may have originated as melts of foundered lower crust, withsubsequent interaction with mantle peridotite. Group 3 dikesare shoshonitic in composition with relatively low (87Sr/86Sr)ivalues (0·7061–0·7063), and negative Nd(t)(–13·2 to –13·4) and Hf(t) (–11·0to –11·5) values, and were derived by partial meltingof an ancient, re-enriched, refractory lithospheric mantle inthe garnet stability field. The geochemical and geochronologicaldata presented here indicate that Late Triassic magmatism occurredin an extensional setting, most probably related to post-orogeniclithospheric delamination. KEY WORDS: mafic dike; asthenospheric mantle; lithospheric mantle; delamination; North China Craton  相似文献   

8.
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   

9.
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   

10.
Numerous dykes of ultramafic lamprophyre (aillikite, mela-aillikite,damtjernite) and subordinate dolomite-bearing carbonatite withU–Pb perovskite emplacement ages of 590–555 Ma occurin the vicinity of Aillik Bay, coastal Labrador. The ultramaficlamprophyres principally consist of olivine and phlogopite phenocrystsin a carbonate- or clinopyroxene-dominated groundmass. Ti-richprimary garnet (kimzeyite and Ti-andradite) typically occursat the aillikite type locality and is considered diagnosticfor ultramafic lamprophyre–carbonatite suites. Titanianaluminous phlogopite and clinopyroxene, as well as comparativelyAl-enriched but Cr–Mg-poor spinel (Cr-number < 0.85),are compositionally distinct from analogous minerals in kimberlites,orangeites and olivine lamproites, indicating different magmageneses. The Aillik Bay ultramafic lamprophyres and carbonatiteshave variable but overlapping 87Sr/86Sri ratios (0·70369–0·70662)and show a narrow range in initial Nd (+0·1 to +1·9)implying that they are related to a common type of parentalmagma with variable isotopic characteristics. Aillikite is closestto this primary magma composition in terms of MgO (15–20wt %) and Ni (200–574 ppm) content; the abundant groundmasscarbonate has 13CPDB between –5·7 and –5,similar to primary mantle-derived carbonates, and 18OSMOW from9·4 to 11·6. Extensive melting of a garnet peridotitesource region containing carbonate- and phlogopite-rich veinsat 4–7 GPa triggered by enhanced lithospheric extensioncan account for the volatile-bearing, potassic, incompatibleelement enriched and MgO-rich nature of the proto-aillikitemagma. It is argued that low-degree potassic silicate to carbonatiticmelts from upwelling asthenosphere infiltrated the cold baseof the stretched lithosphere and solidified as veins, therebycrystallizing calcite and phlogopite that were not in equilibriumwith peridotite. Continued Late Neoproterozoic lithosphericthinning, with progressive upwelling of the asthenosphere beneatha developing rift branch in this part of the North Atlanticcraton, caused further veining and successive remelting of veinsplus volatile-fluxed melting of the host fertile garnet peridotite,giving rise to long-lasting hybrid ultramafic lamprophyre magmaproduction in conjunction with the break-up of the Rodinia supercontinent.Proto-aillikite magma reached the surface only after coatingthe uppermost mantle conduits with glimmeritic material, whichcaused minor alkali loss. At intrusion level, carbonate separationfrom this aillikite magma resulted in fractionated dolomite-bearingcarbonatites (13CPDB –3·7 to –2·7)and carbonate-poor mela-aillikite residues. Damtjernites maybe explained by liquid exsolution from alkali-rich proto-aillikitemagma batches that moved through previously reaction-lined conduitsat uppermost mantle depths. KEY WORDS: liquid immiscibility; mantle-derived magmas; metasomatism, Sr–Nd isotopes; U–Pb geochronology  相似文献   

11.
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   

12.
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   

13.
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   

14.
The petrogenesis of pyroxenite layers within the Beni Bouseraperidotite massif is investigated by means of elemental andNd-Sr-Pb-O-S isotope analyses. The light rare earth element(LREE) depleted nature of many of the pyroxenites, their widevariation in composition, and lack of correlation between incompatibleelements and fractionation indices preclude them from representingcrystallized melts from a peridotitic source. The physical characteristicsof the pyroxenites and their large (greater than a factor of20) range in Ni rule out partial melting as the cause of theirpetrological and geochemical diversity. Major and compatibletrace element geochemistry is consistent with formation of mostof the pyroxenite suite via high-pressure crystal segregationin magma conduits intruding the peridotites. These magmas crystallizedclinopyroxene, orthopyroxene, and garnet. The pressure of crystallizationis constrained to be above {small tilde}45 kbar from the presenceof graphitized diamonds in pyroxenite layers. Lack of correlationbetween fractionation indices and highly incompatible elementsand the wide variation in incompatible element abundances suggestthat the suite did not form from genetically related magmas.The presence of positive and negative Eu anomalies (Eu/Eu* =0•54–2•0) in pyroxenites which crystallizedat pressures much greater than the plagioclase stability field({small tilde} 45 kbar) suggests that the parental magmas originatedfrom precursors which formed in the crust. Oxygen isotope compositionsof coexisting minerals in the pyroxenites indicate high-temperatureequilibration but 18O values vary from +4•9 to + 9•3,ruling out their derivation from the host peridotites or othernormal mantle sources. The extreme O-isotope variation, togetherwith 34S values of up to + 13 in sulphides included within CPXstrongly suggests that the melts from which the pyroxenitescrystallized were derived from hydrothermally altered, subductedoceanic lithosphere. Extreme initial radiogenic isotope variationin the pyroxenites (Nd + 26 to –9 , 87Sr/86Sr 0•7025–0•7110,206Pb/204Pb 18•21–19•90) support such an originbut also require a component with ancient, high U/Pb and Th/Pbin their source to explain the high 7/4 and 8/4 values of somepyroxenites. This component may be subducted hemi-pelagic sediment.Further evidence for a sediment component in the pyroxenitesis provided by isotopically light carbon in the graphite pyroxenites(13C–16 to – 28). Parentdaughter isotopes in thepyroxenites are strongly decoupled, making estimation of formationages speculative. The decoupling occurred recently (<200Ma), probably as a result of partial melting associated withdiapiric upwelling and emplacement of the massif into the crustfrom the diamond stability field. This late partial meltingevent further depleted the pyroxenites in incompatible elements.The variably altered nature of the subducted protolith and complexhistory of trace element fractionation of the pyroxenites haslargely obscured geochemical mixing trends. However, Nd–Pbisotope systematics indicate that incorporation of the componentwith high U/Pb–Th/Pb occurred relatively recently (<200Ma) for some pyroxenites. Other pyroxenites do not show evidencefor incorporation of such a component and may be substantiallyolder. Tectonic, geophysical, and isotopic constraints indicateformation of the pyroxenites in the mantle wedge above a subductingslab during the Cretaceous. Physical and chemical evidence forhigh-pressure fractionation seen in most of the pyroxenitesprecludes them from simply representing ancient subducted oceaniclithosphere, thinned by diffusion. However, the petrologicaland isotopic diversity of the massif support the concept ofa ‘marble cake’ mantle capable of producing theobserved geochemical diversity seen in oceanic magmas. *Present Address: Department of Terrestrial Magnetism, 5241 Broad Branch Road, N.W., Washington, DC 20015 Present address: Department of Geological Sciences, 1066 C.C. Little Building, University of Michigan, Ann Arbor, Michigan 48109  相似文献   

15.
13C/12C ratios have been analysed in graphite adcumulate crystalsassociated with the olivine and orthopyroxene of a suite ofultramafic xenoliths in the alkali basalts of Tissemt (Egg?r?,Algerian Sahara). The 13C of these graphites varies from –24?6to – 14?4 per milk with internal variations of up to 1?6per mille within a given sample. Carbonates, linked to the volcanicphase and precipitated at medium temperatures have 13C valuesfrom –0?8 to + 3?5 and 18O values from 21?6 to 31?5 Thehost lava has a high carbon content of 675 p.p.m. with a global13C of –4?2. It can be separated into three parts: a majorpeak is obtained between 670 and 985 ?C and also liberated byslow acid attack with a 13C of up to +7?3 and representing CO2trapped in the natrolite; a high temperature peak (above 1160?C with 47 p.p.m at –25?8) will represent carbon trappedin silicates and there is an additional carbon not well determinedextracted from 300 ?C to high temperature which represent 215p.p.m. at –23?0 with a possible fraction as low as –68?0.The graphite is interpreted as the result of the precipitationof carbon from an interstitial liquid previously outgassed thensupersaturated by the ongoing crystallization process. The volcanicevent can be considered to a first approximation as remobilizingthe carbon from the xenoliths by oxidation to CO2, subsequentpartial reduction upon cooling and precipitation of carbonateand trapping of residual CO2 within zeolite. Only volatilereducedspecies can be significantly outgassed so that the total 13Cof –4?2 is probably close to (or a little higher than)the original 13C.  相似文献   

16.
The volcanic history of Santo Antão, NW Cape Verde Islands,includes the eruption of basanite–phonolite series magmasbetween 7·5 and 0·3 Ma and (melilite) nephelinite–phonoliteseries magmas from 0·7 to 0·1 Ma. The most primitivevolcanic rocks are olivine ± clinopyroxene-phyric, whereasthe more evolved rocks have phenocrysts of clinopyroxene ±Fe–Tioxide ± kaersutite ± haüyne ± titanite± sanidine; plagioclase occurs in some intermediate rocks.The analysed samples span a range of 19–0·03% MgO;the most primitive have 37–46% SiO2, 2·5–7%TiO2 and are enriched 50–200 x primitive mantle in highlyincompatible elements; the basanitic series is less enrichedthan the nephelinitic series. Geochemical trends in each seriescan be modelled by fractional crystallization of phenocrystassemblages from basanitic and nephelinitic parental magmas.There is little evidence for mineral–melt disequilibrium,and thus magma mixing is not of major importance in controllingbulk-rock compositions. Mantle melting processes are modelledusing fractionation-corrected magma compositions; the modelssuggest 1–4% partial melting of a heterogeneous mantleperidotite source at depths of 90–125 km. Incompatibleelement enrichment among the most primitive magma types is typicalof HIMU OIB. The Sr, Nd and Pb isotopic compositions of theSanto Antão volcanic sequence and geochemical characterchange systematically with time. The older volcanic rocks (7·5–2Ma) vary between two main mantle source components, one of whichis a young HIMU type with 206Pb/204Pb = 19·88, 7/4 =–5, 8/4 0, 87Sr/86Sr = 0·7033 and 143Nd/144Nd= 0·51288, whereas the other has somewhat less radiogenicSr and Pb and more radiogenic Nd. The intermediate age volcanicrocks (2–0·3 Ma) show a change of sources to two-componentmixing between a carbonatite-related young HIMU-type source(206Pb/204Pb = 19·93, 7/4 = –5, 8/4 = –38,87Sr/86Sr = 0·70304) and a DM-like source. A more incompatibleelement-enriched component with 7/4 > 0 (old HIMU type) isprominent in the young volcanic rocks (0·3–0·1Ma). The EM1 component that is important in the southern CapeVerde Islands appears to have played no role in the petrogenesisof the Santo Antão magmas. The primary magmas are arguedto be derived by partial melting in the Cape Verde mantle plume;temporal changes in composition are suggested to reflect layeringin the plume conduit. KEY WORDS: radiogenic isotopes; geochemistry; mantle melting; Cape Verde  相似文献   

17.
A High-K, Mantle Derived Plutonic Suite from 'Linga', near Arequipa (Peru)   总被引：2，自引：0，他引：2  
The Linga Group consists of a suite of Cretaceous high-K calc-alkalinerocks intruded into 2?0 Ga old basement in S.E. Peru. The rocksrange in composition from gabbros, through diorites and grandioritesto granites. Microprobe, major and trace element and isotopedata suggest the suite evolved by fractional crystallization,with plagioclase as the dominant phase and with surprisinglylittle interaction with the pre-existing crust. The rocks yieldan Rb/Sr whole rock isochron of 68 ? 3 Ma with an initial Sr-isotoperatio 0.70516 ? 8, and from three Nd-isotope analyses initialNd = – 1?4 to – 2?0. 18 O increases from 5?0 permil in a gabbro to 7?0 per mil in a granite, and models arepresented which suggest that the suite evolved from parentalmagmas which had 18O = 5?8 to 6?0 per mil, 1.5 per cent K2O,63 p.p.m. Rb, 582 p.p.m. Sr, 35 p.p.m. Ce, 0.38 p.p.m. Ta, 87Sr/86Sr= 0.7052, and 143Nd/144Nd = 0.51247. Trace element considerationsimply that these magmas contain contributions from incompatibleelement enriched upper mantle material and from a componentassociated with subduction. The latter is thought to reflectthe preferential mobilization of alkali and alkaline earth elementsby H2O-rich fluids from the subducted slab, and preliminarycalculations indicate that it was responsible for {small tilde}45 per cent of the Sr and {small tilde} 80 per cent of the Kin the more primitive Linga rocks. However, the isotope datasuggest that while the fluids may be from the subducted slab,the elements in this component may also have been mobilizedfrom the overlying mantle wedge.  相似文献   

18.
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   

19.
The origin of large-volume Yellowstone ignimbrites and smaller-volumeintra-caldera lavas requires shallow remelting of enormous volumesof variably 18O-depleted volcanic and sub-volcanic rocks alteredby hydrothermal activity. Zircons provide probes of these processesas they preserve older ages and inherited 18O values. This studypresents a high-resolution, oxygen isotope examination of volcanismat Yellowstone using ion microprobe analysis with an averageprecision of ± 0·2 and a 10 µm spot size.We report 357 analyses of cores and rims of zircons, and isotopeprofiles of 142 single zircons in 11 units that represent majorYellowstone ignimbrites, and post-caldera lavas. Many zirconsfrom these samples were previously dated in the same spots bysensitive high-resolution ion microprobe (SHRIMP), and all zirconswere analyzed for oxygen isotope ratios in bulk as a functionof grain size by laser fluorination. We additionally reportoxygen isotope analyses of quartz crystals in three units. Theresults of this work provide the following new observations.(1) Most zircons from post-caldera low-18O lavas are zoned,with higher 18O values and highly variable U–Pb ages inthe cores that suggest inheritance from pre-caldera rocks exposedon the surface. (2) Many of the higher-18O zircon cores in theselavas have U–Pb zircon crystallization ages that postdatecaldera formation, but pre-date the eruption age by 10–20kyr, and represent inheritance of unexposed post-caldera sub-volcanicunits that have 18O similar to the Lava Creek Tuff. (3) Youngand voluminous 0·25–0·1 Ma intra-calderalavas, which represent the latest volcanic activity at Yellowstone,contain zircons with both high-18O and low-18O cores surroundedby an intermediate-18O rim. This implies inheritance of a varietyof rocks from high-18O pre-caldera and low-18O post-calderaunits, followed by residence in a common intermediate-18O meltprior to eruption. (4) Major ignimbrites of Huckleberry Ridge,and to a lesser extent the Lava Creek and Mesa Falls Tuffs,contain zoned zircons with lower-18O zircon cores, suggestingthat melting and zircon inheritance from the low-18O hydrothermallyaltered carapace was an important process during formation ofthese large magma bodies prior to caldera collapse. (5) The18O zoning in the majority of zircon core–rim interfacesis step-like rather than smoothly inflected, suggesting thatprocesses of solution–reprecipitation were more importantthan intra-crystalline oxygen diffusion. Concave-downward zirconcrystal size distributions support dissolution of the smallercrystals and growth of rims on larger crystals. This study suggeststhat silicic magmatism at Yellowstone proceeded via rapid, shallow-levelremelting of earlier erupted and hydrothermally altered Yellowstonesource rocks and that pulses of basaltic magma provided theheat for melting. Each post-caldera Yellowstone lava representsan independent homogenized magma batch that was generated rapidlyby remelting of source rocks of various ages and 18O values.The commonly held model of a single, large-volume, super-solidus,mushy-state magma chamber that is periodically reactivated andproduces rhyolitic offspring is not supported by our data. Rather,the source rocks for the Yellowstone volcanism were cooled belowthe solidus, hydrothermally altered by heated meteoric watersthat caused low 18O values, and then remelted in distinct pocketsby intrusion of basic magmas. Each packet of new melt inheritedzircons that retained older age and 18O values. This interpretationmay have significance for interpreting seismic data for crustallow-velocity zones in which magma mush and solidified areasexperiencing hydrothermal circulation occur side by side. Newbasalt intrusions into this solidifying batholith are requiredto form the youngest volcanic rocks that erupted as independentrhyolitic magmas. We also suggest that the Lava Creek Tuff magmawas already an uneruptable mush by the time of the first post-calderaeruption after 0·1 Myr of the climactic caldera-formingeruption. KEY WORDS: Yellowstone; oxygen isotopes; geochronology; isotope zoning; zircon; U–Pb dating; caldera; rhyolite; ion microprobe  相似文献   

20.
Overlap of Karoo and Ferrar Magma Types in KwaZulu-Natal, South Africa   总被引：3，自引：0，他引：3  
A suite of mafic dykes from the Underberg region of southernKwaZulu-Natal (South Africa) were intruded at 178 Ma, coincidentin age with the major Okavango Dyke Swarm of Botswana, and alsocoincident with minor Karoo-related intrusions of the northernand central Lebombo. The dykes are all low-Ti–Zr tholeiites,they trend NW–SE and are presumed to continue into theKaroo central area of the Lesotho Highlands. In many respects,the Underberg dykes are similar to the majority of the low-Ti–Zrvolcanic and subvolcanic intrusions of the Karoo; however, their87Sr/86Sr and Nd isotope ratios are either ‘Ferrar-like’(87Sr/86Sr 0·710; Nd < –3) or transitional betweenKaroo low-Ti–Zr and Ferrar low-Ti magmas. A potentialFerrar source for at least some of the Underberg dykes is supportedby anisotropy of magnetic susceptibility analyses of the dykesuite, which demonstrate absolute flow direction from the SEto the NW, consistent with Gondwana reconstructions. The roleof crustal contamination and combined fractional crystallizationis also demonstrated to have played a key role in the petrogenesisof the Underberg dykes, involving a local upper crust contaminant.However, the composition of the ‘Ferrar-like’ dykescannot be easily explained by AFC processes, but they do demonstratethat melting of a lithospheric mantle source enriched to a smalldegree by subduction-derived fluid was also important. KEY WORDS: dyke; basalt; crustal contamination; large igneous province  相似文献   

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