天山托洋峰花岗质岩石的同位素地球化学特征

分析了西天山托木尔峰地区花岗质岩石和基底岩石的稀土元素,微量元素以及Ｏ、Ｐｂ、Ｓｒ、Ｎｄ同位素组成。本区北部伊犁地块基底岩石的Ｎｄ同位素模式年龄约为１．９Ｇａ,南部南天山褶皱带的约为０．７０５到０．７３３）表明本区花岗质岩石主要为地壳溶融产物。Ｏ、Ｐｂ、Ｓｒ、Ｎｄ同位素组成批示位于伊犁地块和南天山褶皱带的花岗岩源区岩石的Ｎｄ模式年龄都相当于伊犁地壳,但源区性质不同,前者源区δ＾１８Ｏ低,μ值低,Ｔ     

Oxygen, carbon, and strontium isotope geochemistry of diamond-bearing carbonate rocks from Kumdy-Kol, Kokchetav Massif, Kazakhstan

Diamond-bearing carbonate rocks from Kumdy-Kol, Kokchetav massif, Kazakhstan, were strongly altered by fluids flowing through fractures and infiltrating along grain boundaries during exhumation. Alteration includes retrogradation of high-grade silicate assemblages by hydrous minerals, replacement of diamond by graphite and of dolomite by calcite. Diamond-bearing carbonate rocks are among the most intensely altered isotopically with δ¹⁸O_VSMOW values as low as +9‰, δ¹³C_VPDB=−9‰, and ⁸⁷Sr/⁸⁶Sr as high as 0.8050. Evidence of isotopic equilibration between coexisting dolomite and high-Mg calcite during ultrahigh-pressure metamorphism (UHPM) is preserved only rarely in samples isolated from infiltrating fluids by distance from fractures. Isotopic heterogeneity and isotopic disequilibrium are widespread on a hand-specimen scale. Because of this lack of homogeneity, bulk analyses cannot provide definitive measurements of ¹³C/¹²C fractionation between coexisting diamond and carbonate. Our study adequately documents alteration on a scale commensurate with observed vein structures. But, testing the hypothesis of metamorphic origin of microdiamonds has not fully succeeded because our analytical spatial resolution, limited to 0.5 mm, is not small enough to measure individual dolomite inclusions or individual diamond crystals.     

Reaction mechanisms,physical conditions,and mass transfer during hydrothermal alteration of mica and feldspar in granitic rocks from south-central Maine,USA

Samples of granitic rock from south-central Maine contain primary igneous minerals altered by hydrothermal fluids. The reaction mechanisms (by which the over-all mineralogical change during the alteration was accomplished) involve several different mineral-fluid reactions at different reaction sites in the rock. The reactions involve both molecular and charged species in solution. The different reaction sites correspond to alteration of different primary igneous minerals. Biotite is partially converted to chlorite+sphene; microcline to muscovite; plagioclase to various combinations of muscovite, epidote, and calcite. The different reaction sites are linked by exchange of ions: some reaction sites produce ions consumed at other sites and vice versa. Physical conditions during the hydrothermal event are estimated from mineralogical and thermochemical data: P = 3,500 (±300) bars; T =425 ° (± 25 °)C. The fluid was characterized by X _{CO 2} = 0–0.13; ln([K⁺]/[H⁺ ]) = 10.0; ln([Ca²⁺]/[H⁺]²)=9.1; ln([Na⁺]/[H⁺]) = 10.5; Fe/(Fe+Mg) = 0.95. Amounts of secondary minerals in altered rock, when compared to the inferred mineral reactions that formed them, indicate that small but significant amounts (0.01–0.3mol/ 1,000cm³ altered rock) of CO₂, H₂O, H⁺, and K⁺ were added to the granites by fluids during the alteration, as well as lesser amounts (< 0.01–0.03 mol/1,000cm³ altered rock) of Mg²⁺, Fe²⁺, Fe³⁺, Mn²⁺, Na⁺, and Ti⁴⁺. The sole element leached from the granitic rocks during alteration was Ca in amounts 0.1–0.3 mol/1,000 cm³ rock. By estimating the composition of the hydrothermal fluids before and after reaction with the granites and by measuring the amount of material added to or subtracted from the granites during the alteration, the amount and volume of hydrothermal fluid involved can be calculated. Two independent calculations require minimum volumes in the range 100–1,000 cm³ fluid/1,000cm³ altered rock to participate in the hydrothermal event.     

Oxygen isotope study of metamorphic and granitic rocks of the Yanai district in the Ryoke belt,Japan

¹⁸O/¹⁶O ratios have been obtained for 134 whole-rocks and minerals from metamorphic and granitic rocks of the Yanai district in the Ryoke belt, Southwest Japan. The ¹⁸O/¹⁶O ratios of pelitic rocks of the marginal metamorphic zone decrease progressively with increasing metamorphic grade. In the gneiss-granite complex (zone of migmatite [1]), the most characteristic feature of the rocks is that oxygen isotopic homogenization proceeds on both local and regional scales in parallel with “granitization” or chemical homogenization. Granitic rocks of various origin are fairly uniform in isotopic composition with δ ¹⁸O of quartz of 12 to 14‰ (SMOW) and δ ¹⁸O of biotite of 7 to 9‰ and are about 3 to 4‰ enriched in ¹⁸O compared to other Cretaceous granites of non-metamorphic terranes in Japan. The high ¹⁸O/¹⁶O ratios of granitic rocks of this district were discussed in relation to the ¹⁸O-depletion in metasediments. Oxygen isotopic fractionations among coexisting minerals from various rock-types of the gneiss-granite complex indicate that these minerals were formed under near isotopic equilibrium at a temperature of about 600 to 700° C. Some abnormal fractionations of quartz-biotite pairs also were obtained for rocks which had undergone a progressive ¹⁸O-depletion or ¹⁸O-enrichment. This is due to high resistivity of quartz and contrastive susceptibility of biotite to isotopic exchange during metamorphism and “granitization”.     

Early to Middle Devonian granitic and volcanic rocks from the central Gulf of Maine

Cashes Ledge igneous suite in the central Gulf of Maine is represented by 10 granitic and two felsic tuff samples collected from bedrock outcrops using the submersible Alvin in 1971–1972 and archived at the Woods Hole Oceanographic Institute. Laser ablation ICP-MS analyses of zircon grains yielded crystallization ages of 414.9 ± 1.1 Ma and 399.7 ± 1.5 Ma for two alkali feldspar granite samples, 407.0 ± 1.9 Ma for a syenogranite sample, and 384.4 ± 2.3 Ma and 383.9 ± 1.6 Ma for two felsic tuff samples. The samples contain iron-rich mafic minerals, including aegirine-augite, grunerite/ferroedenite, and annite. Most of the samples are alkaline to slightly peralkaline, with high concentrations of SiO₂, Y, Zr, Nb, and REE, strong negative Eu anomalies, and positive epsilon Nd values (1.8 to 3.7). The suite resembles part of a belt of similar Silurian–Devonian rocks with ages between 426 and 370 Ma now recognized in the central part of Avalonia in southeastern New England. They formed in a long-lived, likely extensional regime linked to subduction and subsequent complex transcurrent motions among Ganderia, Avalonia, and Meguma, culminating in the closure of the Rheic Ocean.     

Oxygen isotope studies of early Precambrian granitic rocks from the Giants Range batholith,northeastern Minnesota,U.S.A.

Oxygen isotope studies of granitic rocks from the 2.7 b.y.-old composite Giants Range batholith show that: (1) δ(O¹⁸)_quartz values of 9 to 10 permil characterize relatively uncontaminated Lower Precambrian, magmatic granodiorites and granites; (2) granitic rocks thought to have formed by static granitization have δ(O¹⁸)_quartz values that are 1 to 2 permil higher than magmatic granitic rocks; (3) satellite leucogranite bodies have values nearly identical to those of the main intrusive phases even where they transect O¹⁸-rich metasedimentary wall rocks; (4) oxygen isotopic interaction between the granitic melts and their O¹⁸-rich wall rocks was minimal; and (5) O¹⁸/O¹⁸ ratios of quartz grains in a metasomatic granite are largely inherited from the precursor rock, but during the progression — sedimentary parent → partially granitized parent → metasomatic granite → there is gradual decrease in δ(O¹⁸)_quartz by 1 to 2 permil.     

The oxygen isotope geochemistry of igneous rocks

Oxygen isotope analyses have been obtained for 443 igneous rock and mineral samples from various localities throughout the world. Detailed studies were made on the Medicine Lake, Newberry, Lassen, Clear Lake, S. E. Guatemala, Hawaii and Easter I. volcanic complexes and on the Bushveld, Muskox, Kiglapait, Guadalupe, Duluth, Nain, Egersund, Lac St. Jean, Laramie, Skaergaard, Mull, Skye, Ardnamurchan and Alta, Utah plutonic complexes, as well as upon several of the zoned ultramafic intrusions of S. E. Alaska. Basalts, gabbros, syenites and andesites are very uniform in O¹⁸/O¹⁶, commonly with δ-values of 5.5 to 7.0 per mil. Many rhyolite obsidians, particularly those from oceanic areas and the Pacific Coast of the United States, also lie in this range; this indicates that such obsidians are differentiates of basaltic or andesitic magma at high temperatures (about 1,000° C). They cannot represent melted sialic crust. The only plutonic granites with such low δ-values are some of the hypersolvus variety, suggesting that these also might form by fractional crystallization. Obsidians from the continental interior, east of the quartz-diorite line, have higher δ-values. This is compatible with their having assimilated O¹⁸-rich sialic crust. A correlation generally exists between the O¹⁸/O¹⁶ ratios of SiO₂-rich differentiates and the chemical trends in volcanic complexes. High O¹⁸/O¹⁶ ratios accompany those trends having the lower Fe/Mg ratios, while ferrogabbro trends are associated with depletion in O¹⁸. Variations in oxygen fugacity may be responsible for these effects, as abundant early precipitation of magnetite should lead to both O¹⁸-enrichment and Fe-depletion in later differentiates. Plutonic granites have higher O¹⁸/O¹⁶ ratios than their volcanic equivalents, because (a) their differentiation occurred at much lower temperatures, or (b) they are in large part derived from O¹⁸-rich sialic crust by partial melting or assimilation. Also, the oxygen isotope fractionations among coexisting minerals are distinctly larger in plutonic rocks than in volcanic rocks. This is in keeping with their lower crystallization temperatures and their longer cooling history, which promotes post-crystallization oxygen isotope exchange. Hydrated obsidians and perlites have δO¹⁸-values that are much different from their primary, magmatic values. A correlation exists between D/H and O¹⁸/O¹⁶ ratios in hydrated volcanic glass from the western U.S.A., proving that the isotopic compositions are a result of exchange with meteoric waters. The O¹⁸ contents of the glasses appear to be about 25 per mil higher than their associated waters; hence, these hydrated glasses have not simply absorbed H₂O, but they have exchanged with large quantities of it. The igneous rocks from Mull, Skye, Ardnamurchan and the Skaergaard intrusion are all abnormally depleted in O¹⁸ relative to “normal” igneous rocks. This is a result of their having exchanged at high temperatures with meteoric water that was apparently abundant in the highly jointed plateau lavas into which these igneous rocks were intruded. In part, this exchange occurred with liquid magma and in part with the crystalline rock; in the latter case the feldspar was more easily exchanged and has become much more depleted in O¹⁸ than has coexisting quartz or pyroxene. The later differentiates of the Muskox intrusion are markedly O¹⁸-rich, but this is not a result of fractional crystallization. It is in large part a result of deuteric exchange between feldspars and an oxygen-bearing fluid (H₂O ?) that was either O¹⁸-rich or had a relatively low temperature. This phenomenon was also observed in a number of granophyres from other localities, particularly those containing brick-red alkali feldspar. The exchanged feldspars in all these examples are turbid or cloudy, and may be filled with hematite dust. It is concluded that most such feldspar in nature is the result of deuteric exchange and is probably drastically out of oxygen isotopic equilibrium with its coexisting quartz.     

Oxygen isotope geothermometers for metamorphic rocks

The Chicago mineral-carbonate oxygen isotope fractionation curves have been combined with mineral-water fractionation data for jadeite, zoisite and rutile and new data for grossular-water to provide a set of self-consistent mineral-pair calibrations. The A coefficients in the equation 1000 In α= A × 10⁶T^-2 of the new mineral-pair fractionations are
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)₃Al₂Si₃O₁₂] can be approximated by those of the grossular end-member. Appropriate substitutions also yield coefficients for the solid-solution minerals: sodic pyroxene and epidote, e.g.
A _{quartz-sodic pyroxene}= 2.75 - 1.06X_jd,
A _{quartz-epidote}= 2.00 + 0.75X_ps
where X _Jd and X _Ps are the mole fractions of the jadeite and pistacite components, respectively.
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ¹⁸O data from minerals of the high-pressure metamorphic rocks of the Sesia Zone of Italy and Cyclades Complex of Greece yield well-constrained mean temperatures of 572 and 478 C, respectively. Type III blueschist metabasalts of the Franciscan Formation of California give mean quartz-garnet temperatures of 354 C.     

A Comparative geochemical study of pelitic schists and metamorphosed carbonate rocks from south-central Maine,USA

Whole-rock major element chemical analyses of progressively metamorphosed impure carbonate rocks and pelitic schists, collected from the same metamorphic terrain, reveal similarities and differences in the chemical response of these rock types to the metamorphic event. Relative to a constant aluminum reference frame, both schist and carbonate exhibit no detectable change in their contents of Fe, Mg, Ti, Si, and Ca with change in metamorphic grade. Carbonate rocks become progressively depleted in K and Na with increasing grade of metamorphism, while schists exhibit no statistically significant change in their contents of K and Na. Both rock types become depleted in volatiles (principally CO₂ and H₂O) with increasing grade.Whole-rock chemical data permit two mechanisms for migration of K and Na from the carbonate rocks during metamorphism: (a) diffusion of alkalis from carbonate to adjacent schist; (b) transport of alkalis by through-flowing metamorphic fluid (infiltration). Mineral equilibria in schist and metacarbonate rock from the same outcrops allow calculation of the affinity for cation exchange between the two rock types during metamorphism. Measured affinities indicate that if mass transport of K and Na occurred by diffusion, chemical potential gradients would have driven the alkalis from schist into carbonate rock. Because diffusion cannot produce the observed chemical trends in the metacarbonates, K and Na are believed to have been removed during metamorphism by infiltration.The disparity in chemical behavior between the pelitic schists and metacarbonate rocks may be a result of enhanced fluid flow through the carbonates. The carbonate rocks may have acted as metamorphic aquifers; the greater flow of fluid through them would then have had a correspondingly greater effect on their whole-rock chemistry.     

Oxygen isotopic study of the Cretaceous granitic rocks in Japan

The ( ¹⁸O values of nine Cretaceous granitic rocks from the low P/T type regional metamorphic zone of Japan are +10.0 to +13.2 relative to SMOW, while ten Cretaceous granitic rocks from the non-metamorphic zone are +7.9 to +9.8. The ¹⁸O-enrichment in the former rocks is mainly attributed to oxygen isotopic exchange between the granitic magma and the surrounding metamorphic rocks during regional metamorphism. The assimilation of ¹⁸O-rich country rocks is also possible in the cases such as gneissose granite and migmatite.The oxygen isotopic ratios of quartz-biotite pairs in the granitic rocks indicate that they are isotopically in near-equilibrium with each other. The quartz-biotite isotopic equilibrium temperatures estimated for these rocks range from 550° to 670° C. Feldspar is occasionally isotopically in disequilibrium with other minerals. This may be caused by exchange of oxygen isotopes between feldspar and hydrothermal or meteoric water after crystallization.     

Zircon Hf isotope perspective on the origin of granitic rocks from eastern Bavaria, SW Bohemian Massif

The petrogenetic potential of in situ laser ablation Hf isotope data from melt precipitated zircons was explored through the analyses of about 700 individual crystals derived from about 20 different granitic intrusions covering the Variscan basement segment of eastern Bavaria, SE Germany. In combination with geochemical features, four major suites of granitic rocks can be distinguished: (1) NE Bavarian redwitzites (52–57 wt% SiO₂, intrusion ages around 323 Ma) have chondritic εHf(t) values (+0.8 to –0.4). The redwitzites are hybrid rocks and the Hf data are permissive of mixing of a mantle progenitor and crustal melts. (2) Various intermediate rock types (dioritic dyke, granodiorite, palite, 59–63 wt% SiO₂, 334–320 Ma) from the Bavarian Forest yield negative εHf(t) values between –3.4 and –5.1. These values which apparently contradict a mantle contribution fingerprint an enriched (metasomatized) mantle component that was mixed with crustal material. (3) Voluminous, major crust forming granites sensu stricto (67–75 wt% SiO₂, 328–298 Ma) are characterized by a range in εHf(t) values from –0.5 to –5.6. Different crustal sources and/or modification of crustal melts by various input of juvenile material can explain this variation. (4) Post-plutonic (c. 299 Ma) porphyritic dykes of dacitic composition (64–67 wt% SiO₂) from the southern Bavarian Forest have chondritic εHf(t) values (+0.6 to –1.1) and display large intergrain Hf isotope variation. The dykes form a separate petrogenetic group and the Hf data suggest that the zircons crystallized when a pristine mantle-derived parental melt was modified by infiltration of crustal material. The zircon Hf data form a largely coherent positive array with the whole-rock Nd data and both systems yield similar two-stage depleted mantle model ages (1.1–1.7 Ga).     

Geochemistry of biotites from granitic rocks,Northern Portugal

The biotites from a series of rocks ranging in composition from tonalite to granite have been analysed for both major and trace elements.The relations between chemical composition and paragenesis of the biotites are studied. Most biotites co-exist with potassium feldspar and ilmenite. Variations in composition can be correlated with the occurrence of amphibole, primary muscovite and aluminosilicates in the rocks.Variation diagrams of the trace element contents and element ratios of biotite are compared to those of the host rocks. Fractionation of elements can be defined more accurately as the influence of other mineral phases is eliminated.Variations in the proportions of the octahedrally co-ordinated Al, Ti and Fe³⁺ are correlated with the conditions of crystallization and comparisons made with biotites from other suites of calc-alkali rocks.In the light of the experimental data available, the petrographic observations and the chemical data it is apparent that biotites crystallized from systems in which fO₂ was buffered, its values remaining close to that of the buffer FMQ. From the same data, a temperature of 800°C for fO₂ = 10^?14to 10^?15 bars is deduced as prevalent during the crystallization of the tonalites while for the granites, at a temperature of crystallization of 680°C, fO₂ = 10^?16to 10^?18 bars.A calc-alkali trend of fractionation is therefore apparent with decreasing fO₂ while fH₂O₂ remains relatively high.     

Oxygen isotope study of metamorphic rocks from the Ouégoa district,New Caledonia

48 minerals from 18 in situ metamorphic rocks (mostly metasediments) from the Ouégoa district have been studied. Particular emphasis was placed on obtaining isotopic data for quartz, calcite and muscovite but some pyroxenes and amphiboles were also examined. Data for Ouégoa rocks show they have tended to be isotopically homogenized by metamorphism and that the effect of increasing metamorphism is to progressively deplete the rocks of heavy C and O isotopes. These results indicate that during metamorphism the rocks isotopically exchanged through the medium of a widespread oxygen-carrying fluid phase. Tentatively assigned temperatures obtained from isotopic data for quartz-calcite and quartz-muscovite pairs, using the calibration curves of Epstein and Taylor (1967), indicate lawsonite in the Ouégoa schists to be stable over a temperature range of 250 to 400° C and epidote from ca. 380° to at least 550° C. Temperatures for metamorphic zones in Ouégoa blueschists closely parallel those obtained for Type III and IV glaucophane-bearing rocks from Ward Creek, California (Taylor and Coleman, 1968). The measured tectonic thickness of lawsonite-bearing schists has been used to calculate a lithostatic pressure increment of 2 Kb and geothermal gradient of 20° C per km for the lawsonite zone. Comparison of lithostatic pressure increment with total pressure increment estimated from the stability relations of lawsonite over the temperature range 250–400° C (3.5 Kb Nitsch, 1972) suggest P _total ≠ P _lithostatic and that that the pressure of the fluid phase may have exceeded lithostatic pressure.     

Late Pleistocene mammoth remains from Coastal Maine, USA

Remains identified as those of a woolly mammoth (Mammuthus primigenius) dated at 12,200 ± 55 ¹⁴C yr B.P. were recovered while excavating in a complex sequence of glaciomarine sediments in Scarborough, Maine, USA. The mammoth was found in the top meter of a fossiliferous unit of mud and sand laminites. These sediments were deposited during a marine regressive phase following the transgression that accompanied northward retreat of the margin of the Laurentide ice sheet. A Portlandia arctica valve from the underlying transgressive unit provides a minimum age of 14,820 ± 105 ¹⁴C yr B.P. for local deglaciation. The mammoth, an adult female, died in midwinter with no evidence of human involvement. Tusk growth rates and oxygen-isotope variation over the last few years of life record low seasonality. The mammoth was transported to the site as a partial carcass by the late-glacial proto-Saco River. It sank in a near-shore setting, was subjected to additional disarticulation and scattering of elements, and was finally buried in sediments reworked by the shallowing sea.     

新疆阿拉套山东部后碰撞岩浆活动的时代、地球化学性质及其对陆壳垂向增长的意义

新疆阿拉套山南坡分布有大量花岗质岩浆岩,其中东部博乐地区的花岗质岩浆岩可以分为北部花岗岩、南部花岗岩、晚期岩脉和流纹岩四类。激光探针单颗粒锆石微区U-Pb同位素定年分析确定,北部岩体、南部岩体的侵位时代分别为 298．4±5．7Ma、292．4±4．9Ma,流纹岩喷出时代为270．7±6．5Ma,而岩脉的全岩Rb-Sr等时线年龄为285±13Ma(MSWD =0．52)。这四类花岗质岩石总体的地球化学性质相似,都属于准铝质到过铝质的后碰撞高钾钙碱性花岗岩,均以高的正εNd(T)值为特征。地球化学特征显示,这四类花岗质岩石具有同源岩浆分异演化的特点。从早到晚,前三类花岗岩中Ba、Sr、 P、Eu和Ti亏损程度增加,(La/Yb)n比值下降到接近1,岩浆温度逐渐降低,而εNd(T)值呈升高趋势。最晚形成的流纹岩中 Ba、Sr、P、Eu和Ti亏损程度减小,(La／Yb)n比值升高,岩浆温度再次升高,而εNd(T)值降低,ISr值升高,可能代表另一期岩浆活动的开始。这些花岗质岩石均具有高的εNd(T)值(2．10-5．18)和较年轻的Nd同位素模式年龄(TDM2=0．60-0．87 Ga), 显示该区花岗质岩石地幔物质组分含量较高。地幔物质的加入导致博乐地区大陆地壳的垂向增长．这与新疆北部300Ma 左右地壳垂向增长的过程是一致的。     

Oxygen isotope geochemistry of the Mesozoic volcanics of the Etendeka Formation,Namibia

The Etendeka Formation volcanics consist of a bimodal association of basalts and quartz latites. Forty three new whole rock oxygen isotope analyses are reported for all the major magma types. All the rocks except a minor suite of dolerites have higher ¹⁸O values than normal mantle. The basic rocks (average of 29=8.8) have significantly different ¹⁸O to the acid rocks (average of 10=14.4) These data are apparently consistent with previously published petrogenetic models, which propose that the basalts were affected by crustal contamination and that the quartz latites are crustally derived. However, mineral oxygen data show that there is significant oxygen isotopic disequilibrium between phenocryst and whole rock, the latter being significantly higher in most cases. One of the basic magma types (the Tafelberg basalts) shows mutual positive correlations between ¹⁸O, SiO₂ and _Sr. If these correlations are due to crustal contamination, then as much as 45% contamination is required by material having a ¹⁸O value of 15 which is the maximum observed value in the Damaran basement rocks. In the absence of pyroxene phenocryst ¹⁸O data for the high _Sr Tafelberg basalts (they are aphyric), it is not possible to confirm that contamination has taken place. An alternative explanation is that the correlation between _Sr and SiO₂ resulted from assimilation coupled with fractional crystallization (AFC) (before emplacement). Post-eruption alteration resulted in a correlation between SiO₂ ¹⁸O because the material with the most Si-O bonds was able to concentrate ¹⁸O more effectively. The limited mineral data for the quartz latites suggests that there is some source heterogeneity. A pyroxene ¹⁸O value of 10% for a southern Etendeka quartz latite is consistent with a crustal source.     

佳木斯地块东部二叠纪花岗岩体的锆石U-Pb年代学、地球化学特征及其地质意义

正近十几年来,在佳木斯地块内部相继发现了一套二叠纪花岗岩,其中的锆石年龄介于254～270 Ma之间(吴福元等,2001),同时确定了地块东缘广泛发育二叠纪火山岩,锆石年龄介于263～293 Ma(孟恩等,2008)。这套岩浆岩组合普遍具有活动大陆边缘岩浆弧成因的地球化学特点(于介江等,2013),表明佳木斯地块作为东北晚古生代大陆板块的东部大陆边缘,在二叠纪期间经历了与俯冲作用有关的活动大陆边缘演化过程。为进一步揭示二     

胶南桃行超高压变质岩的氧同位素地球化学及其年代学制约

对苏鲁超高压变质带内诸城桃行地区榴辉岩及其花岗片麻岩围岩进行了单矿物氧同位素组成分析和锆石U-Pb定年。氧同位素组成显示出不均一亏损~(18)O的特征。石英-石榴石等高温矿物对的氧同位素温度为600～950℃,指示它们在榴辉岩相变质条件下达到并保存了氧同位素平衡。而部分石英-长石和白云母-金红石等矿物对的氧同位素温度为350～570℃,指示它们在峰期变质之后的角闪岩相退变质过程中达到并保存了同位素退化交换再平衡。锆石氧同位素组成低达-1.3‰～4.2‰,对这种低δ~(18)O值进行锆石U-Pb定年,分别得到762～834Ma的原岩年龄和202～249Ma的变质年龄。因此,桃行低δ~(18)O值锆石形成于新元古代(700～800Ma)的低δ~(18)O值岩浆。这种低δ~(18)O值岩浆是由于变质岩原岩经历新元古代高温大气降水热液蚀变后再部分熔融所形成。对于在角闪岩相退变质之后保存了封闭体系的花岗片麻岩样品(石英-长石矿物对温度为355～405℃),石榴石在榴辉岩相变质温度下达到并保存了氧同位素平衡(石英-石榴石矿物对温度为685℃),指示石榴石中Sm-Nd体系在同样的变质务件下也达到了平衡。因此,花岗片麻岩中石榴石-斜长石-全岩的Sm-Nd等时线年龄215±11Ma与锆石变质边的三叠纪年龄(202～249Ma)一样,代表了榴辉岩相峰期变质后的冷却年龄。而花岗片麻岩中石英-钾长石和石英-斜长石矿物对处于氧同位素不平衡状态,同时钾长石和斜长石相对于样品中其它矿物异常亏损~(18)O,指示在角闪岩相退变质之后体系曾经开放,岩石受到低~(18)O流体在低温和中温下(200～400℃)的热液蚀变。这种奈件下矿物氧同位素的退化交换是由表面反应机制控制,与Nd的扩散机制不同,因此氧同位素平衡无法制约Sm-Nd矿物等时线的有效性。