首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 765 毫秒
1.
Numerous minette dykes intersect the Precambrian crystallinebasement of Schirmacher Oasis, East Antarctica. This study presentsnew Sr, Nd, Pb and O isotope data for 11 minette samples fromfour different dykes. The samples are characterized by relativelyhigh 87Sr/86Sr (0·7077–0·7134), 207Pb/204Pb(15·45–15·55) and 208Pb/204Pb (37·8–39·8),combined with low 143Nd/144Nd (  相似文献   

2.
This study explores the origin and geochemical evolution ofapatite, monazite, and xenotime along two metamorphic traverses.The first, from the Kigluaik Mountains, Seward Peninsula, Alaska,consists of a localized (85 cm) orthopyroxene–clinopyroxene-bearingdehydration zone. The second consists of orthopyroxene ±clinopyroxene-bearing granulite facies metabasite layers interlayeredwith metapelites over a 3–4 km traverse, along the ValStrona, Ivrea–Verbano Zone, Northern Italy (IVZ). In bothdehydration zones small Th- and U-poor inclusions of monaziteand/or xenotime occur in the apatite. These inclusions are metasomaticallyinduced and nucleated within the apatite via the coupled substitutionsNa+ + (Y + REE)3+ = 2 Ca2+ and Si4+ + (Y + REE)3+ = P5+ + Ca2+.These are not present in apatite from the original amphibolitefacies gneiss. Apatite, in both dehydration zones, also showsa relative increase in both F and Cl compared with apatite fromthe amphibolite facies zone. Granulite facies metabasites inthe IVZ also contain isolated monazite grains, which range fromuniform to complexly zoned in Th the (13–30·1 mol% ThSiO4). These are the product of breakdown and subsequentmobilization of the lanthanides and actinides from monazite-(Ce)in the metapelite layers into the metabasite layers at the startof granulite facies metamorphism. KEY WORDS: apatite; monazite; xenotime; KCl–NaCl brines; metasomatism; phosphate minerals; charnockite–enderbite; granulite facies metamorphism  相似文献   

3.
Consistent core-to-rim decreases of 87Sr/86Sr ratios and coincidentincreases in Sr concentrations in plagioclase phenocrysts ofvarying size (  相似文献   

4.
Quartz–calcite sandstones experienced the reaction calcite+ quartz = wollastonite + CO2 during prograde contact metamorphismat P = 1500 bars and T = 560°C. Rocks were in equilibriumduring reaction with a CO2–H2O fluid with XCO2 = 0·14.The transition from calcite-bearing, wollastonite-free to wollastonite-bearing,calcite-free rocks across the wollastonite isograd is only severalmillimeters wide. The wollastonite-forming reaction was drivenby infiltration of quartz–calcite sandstone by chemicallyreactive H2O-rich fluids, and the distribution of wollastonitedirectly images the flow paths of reactive fluids during metamorphism.The mapped distribution of wollastonite and modeling of an O-isotopeprofile across a lithologic contact indicate that the principaldirection of flow was layer-parallel, directed upward, withany cross-layer component of flow <0·1% of the layer-parallelcomponent. Fluid flow was channeled at a scale of 1–100m by pre-metamorphic dikes, thrust and strike-slip faults, foldhinges, bedding, and stratigraphic contacts. Limits on the amountof fluid, based on minimum and maximum estimates for the displacementof the wollastonite reaction front from the fluid source, are(0·7–1·9) x 105 cm3 fluid/cm2 rock. Thesharpness of the wollastonite isograd, the consistency of mineralthermobarometry, the uniform measured 18O–16O fractionationsbetween quartz and calcite, and model calculations all arguefor a close approach to local mineral–fluid equilibriumduring the wollastonite-forming reaction. KEY WORDS: contact metamorphism, fluid flow, wollastonite, oxygen isotopes, reaction front  相似文献   

5.
Neogene plateau lavas in Patagonia, southern Argentina, eastof the volcanic gap between the Southern and Austral VolcanicZones at 46·5° and 49·5°S are linked withasthenospheric slab window processes associated with the collisionof a Chile Ridge segment with the Chile Trench at 12 Ma. Thestrong ocean-island basalt (OIB)-like geochemical signatures(La/Ta <20; Ba/La <20; 87Sr/86Sr = 0·7035–0·7046;143Nd/144Nd = 0·51290–0·51261; 206Pb/204Pb= 18·3–18·8; 207Pb/204Pb = 15·57–15·65;208Pb/204Pb = 38·4–38·7) of these Patagonianslab window lavas contrast with the mid-ocean ridge basalt (MORB)-like,depleted mantle signatures of slab window lavas elsewhere inthe Cordillera (e.g. Antarctic Peninsula; Baja California).The Patagonian lavas can be divided into a voluminous  相似文献   

6.
LIU  WEI 《Journal of Petrology》2000,41(9):1455-1466
18O/16O and D/H isotope compositions are reported for coexistingquartz, feldspar and biotite from four lithological units withinthe Aral granite batholith, Altay Mts of China. The data exhibita reversed and an anomalously large positive quartz–feldspar18O/16O fractionation. These two 18O/16O fractionations, togetherwith a marked decrease in the D values of biotite, are interpretedin terms of a model involving two stages of isotopic exchangewith aqueous fluids. The first stage of 18O/16O exchange withan 18O-rich aqueous fluid occurred during subsolidus cooling.Kinetic effects of the first stage of 18O/16O exchange are characterizedby the reversed quartz–feldspar 18O/16O fractionationthat was recorded in the megacrystic coarse-grained granitesof Group I and the megacryst-bearing medium- to coarse-grainedgranites of Group II. Robust parameters for the first stageof exchange are obtained by modelling on the hypothesis of initial18O/16O heterogeneity in the granite plus subsolidus 18O/16Oexchange. The spread in the measured 18O values of quartz reflectsthe initial heterogeneity of the granite. Calculated isochronsillustrate that an initially heterogeneous system reacting withan externally buffered fluid can generate arrays that mimicisotherms. The second stage of isotopic exchange with 18O- andD-depleted meteoric water occurred after magma solidification,resulting in the anomalously large positive quartz–feldspar18O/16O fractionation and a marked decrease in the D valuesof biotite. These kinetic effects have been recorded in thefiner-grained granites of Groups III and IV. However, the coarser-grainedgranites of Groups I and II have essentially survived the secondstage of 18O/16O exchange. KEY WORDS: Altay; granite; initial 18O/16O heterogeneity; pseudoisotherm; quartz–feldspar 18O/16O reversal  相似文献   

7.
We present elemental and isotopic (Sr–Nd–Pb–Hf–Os–He)data on primitive alkalic lavas from the Prinsen af Wales Bjerge,East Greenland. Stratigraphical, compositional and 40Ar–39Ardata indicate that this inland alkalic activity was contemporaneouswith the upper parts of the main tholeiitic plateau basaltsand also post-dated them. The alkalic rocks show a marked crustalinfluence, indicating establishment of new magmatic plumbingsystems distinct from the long-lived coastal systems that fedthe relatively uncontaminated plateau basalts. The least contaminatedlavas have high 3He/4He isotope ratios (R/RA 12·4–18·5),sub-chondritic 187Os/188Osi (0·120–0·126),low  相似文献   

8.
FERRY  JOHN M. 《Journal of Petrology》1995,36(4):1039-1053
Contact-mctamorphic assemblages in ophicarbonate from the Bergellaureole correspond either to model isobaric invariant T-XCO2points [Atg-Cal-Di-Tr-Fo (6 samples) and Atg-Cal-Tr-Fo-Dol (2)]or to isobaric univariant T-XCO2, curves [Tr-Cal-Di-Atg (18),Tr-Dol-Atg-Cal (1), Atg-Cal-Fo-Di (1), and Atg-Cal-Tr-Fo (1)].Calcite-dolomite thermometry and mineral-fluid equilibria inthe invariant assemblages record T=440–540C at P=3•5kbar. Equilibrium metamorphic fluids were very H2O rich withX CO2,=0•001–0•027. In the invariant assemblagesTr + Fo were produced by prograde decarbonation-dehydrationreactions. In contrast, measured modes and reaction texturesin samples with univariant assemblages indicate thai Tr wasproduced by carbonation reactions. The apparent paradox of simultaneousdecarbonation reactions in the model isobaric invariant assemblagesand carbonation reactions in univariant assemblages is resolvedby local mineral-fluid equilibrium and fluid flow through ophicarbohatesin the direction of decreasing temperature as the aureole heated.Time-integrated flux (q) was computed from measured reactionprogress in 28 samples for models of both horizontal and verticaldown-temperature flow. Results are similar, with q decreasingrapidly from (0•2–5•1) 105 cm3 fluid/cm2 rock1•3–1•7 km from the intrusion to 0–0•6105cm3/cm2 at 1•8–4•0 km. The decrease in q ismore consistent with vertical than horizontal flow. Variationsin time-integrated flux of more than an order of magnitude arerecorded by samples from the same outcrop. The absence of carbonatein adjacent metaperidotite indicates that flow was confinedto the ophicarbonate. Channelized, spatially heterogeneous,vertical flow can be explained by the brecciation and strongvertical foliation of the ophicarbonate relative to surroundingmassive metaperidotite. Generation of metamorphicfluids by decarbonation-dehydrationreactions within the ophicarbonates explains larger averageflux 1–2 km from the intrusion compared with more distalpoints. KEY WORDS: Bergell; contact metamorphism; fluid flow; ophicarbonate *Telephone: (410) 516-8121. Fax: (410) 516-7933  相似文献   

9.
Petrogenetic models for the origin of lamproites are evaluatedusing new major element, trace element, and Sr, Nd, and Pb isotopedata for Holocene lamproites from the Gaussberg volcano in theEast Antarctic Shield. Gaussberg lamproites exhibit very unusualPb isotope compositions (206Pb/204Pb = 17·44–17·55and 207Pb/204Pb = 15·56–15·63), which incommon Pb isotope space plot above mantle evolution lines andto the left of the meteorite isochron. Combined with very unradiogenicNd, such compositions are shown to be inconsistent with an originby melting of sub-continental lithospheric mantle. Instead,a model is proposed in which late Archaean continent-derivedsediment is subducted as K-hollandite and other ultra-high-pressurephases and sequestered in the Transition Zone (or lower mantle)where it is effectively isolated for 2–3 Gyr. The high207Pb/204Pb ratio is thus inherited from ancient continent-derivedsediment, and the relatively low 206Pb/204Pb ratio is the resultof a single stage of U/Pb fractionation by subduction-relatedU loss during slab dehydration. Sr and Nd isotope ratios, andtrace element characteristics (e.g. Nb/Ta ratios) are consistentwith sediment subduction and dehydration-related fractionation.Similar models that use variable time of isolation of subductedsediment can be derived for all lamproites. Our interpretationof lamproite sources has important implications for ocean islandbasalt petrogenesis as well as the preservation of geochemicallyanomalous reservoirs in the mantle. KEY WORDS: lamproites; Pb isotopes; mantle Transition Zone; subducted sediment; anomalous mantle reservoirs  相似文献   

10.
La Pacana is one of the largest known calderas on Earth, andis the source of at least two major ignimbrite eruptions witha combined volume of some 2700 km3. These ignimbrites have stronglycontrasting compositions, raising the question of whether theyare genetically related. The Toconao ignimbrite is crystal poor,and contains rhyolitic (76–77 wt % SiO2) tube pumices.The overlying Atana ignimbrite is a homogeneous tuff whose pumiceis dacitic (66–70 wt % SiO2), dense (40–60% vesicularity)and crystal rich (30–40 % crystals). Phase equilibriaindicate that the Atana magma equilibrated at temperatures of770–790°C with melt water contents of 3·1–4·4wt %. The pre-eruptive Toconao magma was cooler (730–750°C)and its melt more water rich (6·3–6·8 wt% H2O). A pressure of 200 MPa is inferred from mineral barometryfor the Atana magma chamber. Isotope compositions are variablebut overlapping for both units (87Sr/86Sri 0·7094–0·7131;143Nd/144Nd 0·51222–0·51230) and are consistentwith a dominantly crustal origin. Glass analyses from Atanapumices are similar in composition to those in Toconao tubepumices, demonstrating that the Toconao magma could representa differentiated melt of the Atana magma. Fractional crystallizationmodelling suggests that the Toconao magma can be produced by30% crystallization of the observed Atana mineral phases. Toconaomelt characteristics and intensive parameters are consistentwith a volatile oversaturation-driven eruption. However, thelow H2O content, high viscosity and high crystal content ofthe Atana magma imply an external eruption trigger. KEY WORDS: Central Andes; crystal-rich dacite; eruption trigger; high-silica rhyolite; zoned magma chamber  相似文献   

11.
Kornerupine and associated minerals in 31 samples of high-graderocks relatively rich in Al and Mg were analysed by wet chemistry,ion microprobe mass analyser, electron microprobe and X-raypowder diffraction. For 11 samples of kornerupine and threesamples of biotite (F only) analysed by both wet chemical andion microprobe methods, the best agreement was obtained forB2O3, whereas the ion microprobe Li2O values were systematicallysomewhat higher than the wet chemical values. The wet chemicalmethods give Li2O=0–0?19 wt.%; BeO=0–0?032 wt.%;B2O3=0–4?01 wt.%; and F=0?07–0?77 wt.% in kornerupine,whereas ion microprobe analyses on other kornerupines give valuesup to 0?35 wt.% Li2O, O066 wt.% BeO, and 4?72 wt.% B2O3. Thesum B+Al+Fe3++Cr is close to 6?9 atoms per 22 (O, OH, F) or21?5 (O) in kornerupine. In general, Li/Fe ratios decrease as follows: kornerupine ?sapphirinebiotite> Crd (Na<0?03 per 18 oxygens)>tourmaline, garnet,orthopyroxene. However, for cordierite with Na>004, Li/Fedecreases as follows: cordierite>kornerupine. Sapphirineand sillimanite are the only associated minerals to incorporatesignificant boron (0?1–0?85 wt.% B2O3) and then only whenthe single site for B in kornerupine is approaching capacity.Sillimanite B2O3 contents increase regularly with kornerupineF. Fractionation of fluorine increases as follows: kornerupine<biotite<tourmaline,and Kkrn-BtD=(F/OH)Krn/(F/(OH)Bt (assuming ideal anion composition)increases with biotite Ti. Kornerupine B2O3 content is a measureof B2O3 activity in associated metamorphic fluid, whereas sillimaniteB2O3 content increases with temperature, exceeding 0?4 wt.%whenT=900?C at very low water activities. New data on 11 kornerupines and literature data indicate thatthe unit cell parameters a, c, and V decrease with increasingB content and b, c, and V increase with increasing Fe3+ content.In Fe3+-poor kornerupines, b increases with Mg and with (Mg+ Fe2+) but the effect of Mg on b via the substitution VIMg+IVSi=VIAl+IVAloverwhelms the effect of Fe2+=Mg substitution.  相似文献   

12.
During the mid-Cretaceous, extensive magmatism occurred in theIndian Ocean to form volcanic portions of the southern and centralKerguelen Plateau, Elan Bank and Broken Ridge. Basalt was eruptedalso along the rifted margin of eastern India (Rajmahal). Weinvestigated the ages of these Indian basalts using 40Ar/39Arincremental-heating experiments on whole rocks. Our resultsare consistent with the hypothesis that the lava pile of  相似文献   

13.
Phase relations for the bulk compositions 3CaO·2FeOx·3SiO2+excessH2O and CaO·FeOx·2SiO2+excess H2O were determinedusing conventional hydrothermal techniques with solid phaseoxygen buffers to control fO2. Andradite, Ca3Fe3+2Si3O12, synthesized above 550 °C hasan average unit cell edge, ao, of 12.055±0.001 Å,and an index of refraction, n, of 1.887±0.003. Belowthis temperature, ao increases whereas n decreases, indicatingthe formation of a member of the andradite-hydroandradite solidsolution. At 2000 bars Pfluid andradite is stable above an fO2of 1015 bar at 800 °C and 10-32 bar at 400 °C. At lowerfO2 andradite+fluid gives way at successively lower temperaturesto the condensed assemblages magnetite+wollastonite, kirschsteinite(CaFe2+SiO4)+ wollastonite and kirschsteinite+xonotlite (Ca6Si6O17(OH)2). Synthetic hedenbergite, CaFe2+Si2O6, has average unit cell dimensionsof ao = 9.857± 0.004 Å, bo = 9.033±0.002Å, co = 5.254±0.002 Å and ß = 104.82°±0.03°,and refractive indices of n = 1.731±0.003 and n = 1.755±0.005.At 2000 bars Pfiuid, hedenbergite is stable below an fO2 of10-13 bar at 800 °C and 10-28 bar at 400 °C. Above thesefO2 values, hedenbergite+O2 breaks down to andradite+magnetite+quartz. The mineral pair andradite +hedenbergite thus limit the fO2range possible for their joint formation under equilibrium conditions. The hydration of wollastonite to xonotlite occurs at much lowertemperatures than previous experimental work indicated. A tentativehigh temperature limit for this reaction is set at 185°±15°C and 5000±25 bars and 210°±15 °Cand 2000±20 bars. Inasmuch as the growth of xonotlitefrom wollastonite + H2O was never accomplished, this high temperaturelimit does not represent an equilibrium univariant curve. Nine phases were encountered in the study of andradite and hedenbergite.They are andradite, hedenbergite, magnetite, wollastonite, kirschsteinite,xonotlite, quartz, ilvaite, and vapor (fluid). An invariantpoint analysis using the method of Schreinemakers shows thetopologic relations of the reactions involved. The resultinggrid can be used to interpret natural occurrences.  相似文献   

14.
The Takaka Terrane in the South Island of New Zealand containsa well-preserved Cambrian arc system (Devil River Volcanics)that displays a complete assemblage of interbedded low- to high-Karc rocks, back-arc rocks and boninites. Most volcanic rocksare mafic. A coherent dataset was obtained including major elements,trace elements and Sr–Nd–Pb isotope compositionsfrom clinopyroxene and amphibole separates. With time, 207Pb/204Pbin the arc rocks become more unradiogenic and 143Nd/144Nd moreradiogenic, and Th/Yb and La/Yb increase. La/Yb values rangefrom one in the boninites and back-arc rocks to 30 in the high-Karc rocks. Corresponding  相似文献   

15.
Chromite compositions in komatiites are influenced by metamorphicprocesses, particularly above 500°C. Metamorphosed chromiteis substantially more iron rich than igneous precursors, asa result of Mg–Fe exchange with silicates and carbonates.Chromite metamorphosed to amphibolite facies is enriched inZn and Fe, and depleted in Ni, relative to lower metamorphicgrades. Relative proportions of the trivalent ions Cr3+, Al3+and Fe3+ are not greatly modified by metamorphism up to loweramphibolite facies, although minor Fe3+ depletion occurs duringtalc–carbonate alteration at low temperature. SignificantAl is lost from chromite cores above 550°C, as a resultof equilibration with fluids in equilibrium with chlorite. ElevatedZn content in chromite is restricted to rocks with low (metamorphic)Mg/Fe ratios, and is the result of introduction of Zn duringlow-temperature alteration, with further concentration and homogenizationduring prograde metamorphism. Cobalt and Mn also behave similarly,except where carbonate minerals are predominant in the metamorphicassemblage. Chromite at amphibolite facies is typically extensivelyreplaced by magnetite. This is the result of incomplete metamorphicreaction between chromite and chlorite-bearing silicate assemblages.Magnetite compositions at the inner chromite–magnetiteboundary are indicators of metamorphic grade. KEY WORDS: chromite; komatiite; spinel; metamorphism; Zn  相似文献   

16.
Daisen volcano, southwest Japan, has been thought to be an exclusivelydacitic volcano, lavas having trace element patterns with agarnet signature. We studied the basalts at the western footof the volcano and made two unexpected findings. (1) The homogeneityof 87Sr/86Sr in Daisen basalts (Sr isotopic variability  相似文献   

17.
The petrogenesis of calc-alkaline magmatism in the Eocene AbsarokaVolcanic Province (AVP) is investigated at Washburn volcano,a major eruptive center in the low-K western belt of the AVP.New 40Ar/39Ar age determinations indicate that magmatism atthe volcano commenced as early as 55 Ma and continued untilat least 52 Ma. Although mineral and whole-rock compositionaldata reflect near equilibrium crystallization of modal phenocrysts,petrogenetic modeling demonstrates that intermediate compositionmagmas are hybrids formed by mixing variably fractionated andcontaminated mantle-derived melts and heterogeneous siliciccrustal melts. Nd and Sr isotopic compositions along with traceelement data indicate that silicic melts in the Washburn systemare derived from deep-crustal rocks broadly similar in compositionto granulite-facies xenoliths in the Wyoming Province. Our preferredexplanation for these features is that mantle-derived basalticmagma intruded repeatedly in the deep continental crust leadingto fractional crystallization, silicic melt production, andhomogenization of magmas, followed by ascent to shallow reservoirsand crystallization of new plagioclase-rich mineral assemblagesin equilibrium with the intermediate hybrid liquids. The implicationsof this process are that (1) some calc-alkaline magmas may onlybe recognized as hybrids on purely chemical grounds, particularlyin systems where mixing precedes and is widely separated fromcrystallization in space and time, and (2) given the role ascribedto crustal processes at Washburn volcano, the variation betweenrocks that follow calc-alkaline trends in the western AVP andthose that follow shoshonitic trends in the east cannot simplyreflect higher pressures of fractionation to the east in Moho-levelmagma chambers in the absence of crustal interaction. KEY WORDS: petrogenesis; magma mixing; calc-alkaline; Absaroka Volcanic Province; 40Ar/39Ar dates  相似文献   

18.
The upper Triassic Karmutsen metabasites from northeast VancouverIsland, B.C., are thermally metamorphosed by the intrusion ofthe Coast Range Batholith. The amygdaloidal metabasites developedin the outer portion of the contact aureole show a progressivemetamorphism from zeolite to prehnite-pumpellyite facies. Thesize of an equilibrium domain is extremely small for these metabasites,and the individual amygdule assemblages are assumed to be inequilibrium. Two major calcite-free assemblages (+chlorite+quartz)are characteristic: (i) laumontite+pumpellyite+epidote in thezeolite facies and (ii) prehnite+pumpellyite+epidote in theprehnite-pumpellyite facies. The assemblages and compositionsof Ca-Al silicates are chemographically and theoretically interpretedon the basis of the predicted P-T grid for the model basalticsystem, CaO-MgO-A12O3-Fe2O3-SiO2-H2O. The results indicate:(1) local equilibrium has been approached in mineral assemblagesand compositions; (2) the XFe3+ values in the coexisting Ca-Alsilicates decrease from epidote, through pumpellyite to prehnite;(3) with increasing metamorphic grade, the Fe3+ contents ofepidotes in reaction assemblages decrease in the zeolite facies,then increase in the prehnite-pumpellyite facies rocks. Suchvariations in the assemblages and mineral compositions are controlledby a sequence of continuous and discontinuous reactions, andallow delineation of T-XFe3+ relations at constant pressure.The transition from the zeolite to prehnite-pumpellyite faciesof the Karmutsen metabasites is defined by a discontinuous reaction:0·18 laumontite+pumpellyite+0·15 quartz = 1·31prehnite+ 0·78 epidote+0·2 chlorite+ 1·72H2O, where the XFe3+ values of prehnite, pumpellyite and epidoteare 0·03, 0·10 and 0·18, respectively.These values together with available thermodynamic data andour preliminary experimental data are used to calculate theP-T condition for the discontinuous reaction as P = 1·1±0·5 kb and T = 190±30°C. The effectsof pressure on the upper stability of the zeolite facies assemblagesare discussed utilizing T-XFe3+ diagrams. The stability of thelaumontite-bearing assemblages for the zeolite facies metamorphismof basaltic rocks may be defined by either continuous or discontinuousreactions depending on the imposed metamorphic field gradient.Hence, the zeolite and prehnite-pumpellyite facies transitionboundary is multivariant.  相似文献   

19.
ZACK  T.; FOLEY  S. F.; RIVERS  T. 《Journal of Petrology》2002,43(10):1947-1974
Despite the widespread presence of hydrous phases in subduction-related systems, experimental DMin/Fluid trace element valuesfor many hydrous phases are lacking. To fill this gap, we presenta set of DMin/Clinopyroxene values (where Min indicates amphibole,zoisite, phengite, paragonite or apatite) derived from equilibriumparageneses of eclogites from Trescolmen (Central Alps, Switzerland).These data can be combined with experimental data for DClinopyroxene/Fluid,to estimate DMin/Fluid values for the hydrous phases, thus circumventingexperimental problems with the direct determination of suchvalues. We analysed Li, Be, B, Sr, Y, Zr, Nb, Ba, Ce, Nd, Sm,Pb, Th and U in coexisting phases by laser ablation microprobeinductively coupled plasma mass spectrometry. Many of the valuesare extremely low; for example, Nb, Ba, Ce, Th and U are inthe lower ppb range in clinopyroxene. Attainment of equilibriumwas evaluated by textural, and major and trace element characteristics.Non-equilibrated assemblages are common in most eclogite localities,including Trescolmen, and using such samples would lead to thederivation of erroneous values for equilibrium partitioning.However, four of the 10 studied eclogites from Trescolmen havinghomogeneous clinopyroxene compositions and preferred orientationof high-pressure phases yielded consistent DMin/Clinopyroxenevalues in all four samples (where Min indicates amphibole, phengite,paragonite, apatite), and hence were studied in detail. Thelow abundances in some phases result from strong preferentialincorporation of trace elements into other minor phases. Fromthe investigated hydrous phases (amphibole, zoisite, clinozoisite,phengite, paragonite, apatite and talc), zoisite was found tobe the most important carrier of Sr, light rare earth elements,Pb, Th and U, whereas phengite hosts Ba and is, along with clinopyroxeneand paragonite, an important phase for B. However, because oftheir low modal abundance in eclogite-facies rocks, phengiteand paragonite do not control the B whole-rock budget. We inferthat estimated DMin/Clinopyroxene values from equilibrium assemblagescan be used as a good approximation for partition coefficientsunder the given PT conditions (  相似文献   

20.
Sections of Ontong Java Plateau basalt basement in central Malaita(Solomon Islands) are 0·5–3·5 km thick andresemble a much-expanded version of that recovered at OceanDrilling Program Site 807. 40Ar–39Ar ages (121–125Ma) are identical to those for Site 807, southern Malaita, RamosIsland, parts of the island of Santa Isabel, and Deep Sea DrillingProject Site 289; the  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号