where D0 is in µm2/s, X is mole fraction of H2Ot on a single oxygen basis, T is temperature in K, and P is pressure in GPa.H2Ot diffusivities (DH2Ot, in µm2/s) can be calculated from H2Om diffusivity, or directly from the following expression:
At low H2Ot content (up to 2 wt.% if an error of a factor of 2 is allowed), H2Ot diffusivity is approximately proportional to H2Ot content:
where C is H2Ot content in wt.% and C0 is 1 wt.%. The new expressions for H2O diffusion not only reproduce our own data, but also match data in literature from different laboratories and using different methods, indicating good inter-laboratory and multi-method consistency. The new expressions cover a wide range of geological conditions, and can be applied to H2O diffusion in rhyolitic melts in various volcanic and magmatic processes.  相似文献   

14.
Permian bimodal dyke of Tarim Basin, NW China: Geochemical characteristics and tectonic implications   总被引:10,自引:3,他引:10  
Shu-Feng Yang  Zilong Li  Hanlin Chen  M. Santosh  Chuan-Wan Dong  Xing Yu 《Gondwana Research》2007,12(1-2):113
This study reports for the first time the occurrence of bimodal dyke in the Shuigongtuan area of Bachu County, Tarim Basin, NW China. Here, quartz syenite porphyry and diabase dykes occur in direct contact showing bimodal feature. The quartz syenitic porphyry is metaluminous, enriched in K2O + Na2O (10–11 wt.%) and total rare earth elements (REE), with low Mg/(Mg + Fe) ratios, high LREE/HREE, and negative Eu anomalies. The chemical characteristics and tectonic discriminative diagrams show that the rocks have geochemical affinity with A-type granites. The diabase dyke shows 45–52 wt.% SiO2 and Mg/(Mg + Fe) ratio in the range of, with high total REE, high LREE/HREE ratios and lack of Eu anomalies, broadly corresponding to tholeiitic composition. Based on low Y/Nb (as low as 0.4, and less than 1.2), enrichment in LILE and HFSE, and uniform Nb-enrichment patterns in spider diagram for the quartz syenitic porphyry, together with the geochemical patterns of the diabases, this biomodal association is interpreted to be derived from a mantle source and formed under typical within-plate environment. The quartz syenitic porphyry and diabase have Daly gap of 46 wt.%–67 wt.% in SiO2, which is explained through formation under bimodal rifting. The quartz syenitic dyke probably formed during Early Permian (277 Ma) and has geochemical affinity with the Xiaohaizi syenitic body. We propose that magmas sourced from the mantle intruded into middle–upper crust and were emplaced as dykes, which indicate large-scale extension during the Permian in Tarim Basin. The bimodal dyke has genetic affinity with the huge volume of Permian basalts and igneous rocks (248–292 Ma) that occur in the Tarim Basin. The magmatism manifests the culmination of the major thermal event in the Tarim Basin.  相似文献   

15.
Mangerite magmatism associated with a probable Late-Permian to Triassic Hongseong–Odesan collision belt in South Korea     
Chang Whan Oh  Sajeev Krishnan  Sung Won Kim  Yong Wan Kwon 《Gondwana Research》2006,9(1-2):95
The Odesan area in the eastern Gyeonggi Massif, South Korea, consists principally of migmatitic and porphyroblastic gneisses intruded by mangerite. Mafic mangerites with SiO2 contents from 52.40 to 54.20 wt.% have higher FeO* + MgO (14.98–18.28 wt.%) and CaO contents (5.80–7.84 wt.%) but lower total alkali contents (4.74 < Na2O + K2O < 5.80 wt.%) than felsic mangerites (55.9 < SiO2 < 60.61 wt.%, 9.51< FeO* + MgO < 11.62 wt.%, 3.28 < CaO < 5.68 wt.%, 6.72 < Na2O + K2O < 8.05 wt.%). Fe-numbers (FeO* / [MgO + FeO*]) are 0.44–0.47 for mafic mangerites and 0.38–0.42 for felsic mangerites. The mangerites show calc-alkaline affinities in an AFM plot and resemble high-Ba–Sr granitoids with low Rb / Sr ratios of 0.25–0.10. Their MORB-normalized compositions show enrichment in LILE (decoupled LIL/HFS pattern) and negative anomalies in Ti–Nb–Ta. Their geochemical characters are consistent with their formation by partial melting of a basaltic source at temperatures higher than 1025 °C. The mangerites of the present study differ from mangerite formed in a typical within-plate tectonic setting in their high mg# and Sr concentrations and negative Nb and Ta anomalies. Their LILE enrichment and negative Ti–Nb–Ta anomalies could well have been inherited from a pre-collision subduction event. A mean U–Pb zircon age of 257 Ma for the mangerite demonstrates that the tectonic belt connecting the Hongseong and Odesan areas represents a probable extension of the late Permian–Triassic collision belt between the North China and South China blocks into South Korea, with collision occurred earlier in South Korea.  相似文献   

16.
Petrological, organic geochemical and geochemical characteristics of coal from the Soko mine, Serbia   总被引:1,自引:1,他引:0  
Dragana ivoti&#x;  Herman Wehner  Olga Cvetkovi&#x;  Branimir Jovan i&#x;evi&#x;  Ivan Greti&#x;  Georg Scheeder  Angelika Vidal  Aleksandra &#x;ajnovi&#x;  Marko Ercegovac  Vladimir Simi&#x; 《International Journal of Coal Geology》2008,73(3-4):285-306
A petrological, organic geochemical and geochemical study was performed on coal samples from the Soko Mine, Soko Banja basin, Serbia. Ten coal and two carbonaceous clay samples were collected from fresh, working faces in the underground brown coal mine from different parts of the main coal seam. The Lower Miocene, low-rank coal of the Soko Mine is a typical humic coal with huminite concentrations of up to 76.2 vol.%, liptinite less than 14 vol.% and inertinite less than 11 vol.%. Ulminite is the most abundant maceral with variable amounts of densinite and clay minerals. Sporinite and resinite are the most common macerals of the liptinite group. Inertodetrinite is the most abundant maceral of the inertinite group. The mineral-bituminous groundmass identified in some coal samples, and carbonaceous marly clay, indicate sub-aquatic origin and strong bacterial decomposition. The mean random huminite reflectance (ulminite B) for the main coal seam is 0.40 ± 0.05% Rr, which is typical for an immature to early mature stage of organic matter.The extract yields from the coal of the Soko Banja basin ranges from 9413 to 14,096 ppm, in which alkanes constituted 1.0–20.1%, aromatics 1.3–14.7%, asphaltenes 28.1–76.2% and resins 20.2–43.5%. The saturated hydrocarbon fractions included n-C15 to n-C32, with an odd carbon number that predominate in almost all the samples. The contents of n-C27 and n-C29 alkanes are extremely high in some samples, as a contribution of epicuticular waxes from higher plants. Acyclic isoprenoid hydrocarbons are minor constituents in the aliphatic fraction, and the pristane/phytane (Pr/Ph) ratio varies between 0.56 and 3.13, which implies anaerobic to oxic conditions during sedimentation. The most abundant diterpanes were abietane, dehydroabietane and 16α(H)-phyllocladane. In samples from the upper part of the coal seam, diterpanes are the dominant constituents of the alkane fraction. Polycyclic alkanes of the triterpane type are important constituents of alkane fractions. The occurrence of ββ- and αβ-type hopanes from C27 to C31, but without C28, is typical for the Soko Banja coals.The major and trace elements in the coal were analysed using X-ray fluorescence (XRF), and inductively coupled plasma-mass spectrometry (ICP-MS). In comparison with world lignites, using the geometric mean value, the coal from the Soko Banja Basin has a high content of strontium (306.953 mg/kg). Higher values than the world lignites were obtained for Mo (3.614 mg/kg), Ni (8.119 mg/kg), Se (0.884 mg/kg), U (2.642 mg/kg) and W (0.148 mg/kg). Correlation analysis shows inorganic affinity for almost all the major and trace elements, except for S, which has an organic affinity.  相似文献   

17.
The geochemistry of volatile species in melt inclusions and sulfide minerals from Izu-Oshima volcano, Japan     
Kei Ikehata  Atsushi Yasuda  Kenji Notsu 《Mineralogy and Petrology》2010,99(1-2):143-152
Olivine-hosted melt inclusions in the O95 pyroclastic layer of Izu-Oshima volcano, Japan are basaltic to basaltic-andesitic in composition. The negative correlation between SiO2 and H2O in melt inclusions and reverse compositional zoning observed in olivine and other mineral phenocrysts is inferred to arise from mixing between a highly evolved and a less evolved magma. The latter is characterized by the highest S (0.15 wt.%) and H2O (3.4 wt.%) concentrations among those described in reports of previous studies. The S6+/Stotal ratios in melt inclusions were 0.64?–?0.73, suggesting a relatively high oxidation state (NNO + 0.87 at 1150°C). The presence of pyrrhotites, which are found only in titanomagnetite microlites, suggests that sulfide saturation occurred during microlite growth under at a sulfur fugacity (log fS2) value of around + 0.5 for T = 1060°C. The groundmass glass compositions are more evolved (andesitic composition) than any melt inclusions containing high amounts of Cl (0.13 wt.%) but negligible H2O (0.20 wt.%) and S (< 70 ppm), suggesting that Cl was retained in the magma, in contrast to S and H2O, which degassed strongly during magma effusion.  相似文献   

18.
Redox states of lithospheric and asthenospheric upper mantle   总被引:31,自引:7,他引:24  
C. Ballhaus 《Contributions to Mineralogy and Petrology》1993,114(3):331-348
The oxidation state of lithospheric upper mantle is heterogeneous on a scale of at least four log units. Oxygen fugacities ( ) relative to the FMQ buffer using the olivine-orthopyroxene-spinel equilibrium range from about FMQ-3 to FMQ+1. Isolated samples from cratonic Archaean lithosphere may plot as low as FMQ-5. In shallow Proterozoic and Phanerozoic lithosphere, the relative is predominantly controlled by sliding Fe3+-Fe2+ equilibria. Spinel peridotite xenoliths in continental basalts follow a trend of increasing with increasing refractoriness, to a relative well above graphite stability. This suggests that any relative reduction in lithospheric upper mantle that may occur as a result of stripping lithosphere of its basaltic component is overprinted by later metasomatism and relative oxidation. With increasing pressure and depth in lithosphere, elemental carbon becomes progressively refractory and carbon-bearing equilibria more important for control. The solubility of carbon in H2O-rich fluid (and presumably in H2O-rich small-degree melts) under the P,T conditions of Archaean lithosphere is about an order of magnitude lower than in shallow modern lithosphere, indicating that high-pressure metasomatism may take place under carbon-saturated conditions. The maximum in deep Archaen lithosphere must be constrained by equilibria such as EMOG/D. If the marked chemical depletion and the orthopyroxene-rich nature of Archaean lithospheric xenoliths is caused by carbonatite (as opposed to komatiite) melt segregation, as suggested here, then a realistic lower limit may be given by the H2O +C=CH4+O2 (C-H2O) equilibrium. Below C –H2O a fluid becomes CH4 rather than CO2-bearing and carbonatitic melt presumably unstable. The actual in deep Archaean lithosphere is then a function of the activities of CO2 and MgCO3. Basaltic melts are more oxidized than samples from lithospheric upper mantle. Mid-ocean ridge (MORB) and ocean-island basalts (OIB) range between FMQ-1 (N-MORB) and about FMQ +2 (OIB). The most oxidized basaltic melts are primitive island-arc basalts (IAB) that may fall above FMQ+3. If basalts are accurate probes of their mantle sources, then asthenospheric upper mantle is more oxidized than lithosphere. However, there is a wide range of processes that may alter melt relative to that of the mantle source. These include partial melting, melt segregation, shifts in Fe3+/Fe2+ melt ratios upon decompression, oxygen exchange with ambient mantle during ascent, and low-pressure volatile degassing. Degassing is not very effective in causing large-scale and uniform shifts, while the elimination of buffering equilibria during partial melting is. Upwelling graphite-bearing asthenosphere will decompress along -pressure paths approximately parallel to the graphite saturation surface, involving reduction relative to FMQ. The relative will be constrained to below the CCO equilibrium and will be a function of . Upwelling asthenosphere whose graphite content has been exhausted by partial melting, or melts that have segregated and chemically decoupled from a graphite-bearing residuum will decompress along -decompression paths controlled by continuous Fe3+-Fe2+ solid-melt equilibria. These equilibria will involve increases in relative to the graphite saturation surface and relative to FMQ. Melts that finally segregate from that source and erupt on the earth's surface may then be significantly more oxidized than their mantle sources at depth prior to partial melting. The extent of melt oxidation relative to the mantle source may be directly proportional to the depth of graphite exhaustion in the mantle source.  相似文献   

19.
Lamprophyres of the Tomtor Massif: A result of mixing between potassic and sodic alkaline mafic magmas     
L. I. Panina  E. Yu. Rokosova  A. T. Isakova  A. V. Tolstov 《Petrology》2016,24(6):608-625
The paper presents data on inclusions in minerals of the least modified potassic lamprophyres in a series of strongly carbonatized potassic alkaline ultramafic porphyritic rocks. The rocks consist of diopside, kaersutite, analcime, apatite, and rare phlogopite and titanite phenocrysts and a groundmass, which is made up, along with these minerals, of potassic feldspar and calcite. The diopside and kaersutite phenocrysts display unsystematic multiple zoning. Chemically and mineralogically, the rock is ultramafic foidite and most likely corresponds to monchiquite. Primary and secondary melt inclusions were found in diopside, kaersutite, apatite, and titanite phenocrysts and are classified into three types: sodic silicate inclusions with analcime, potassic silicate inclusions with potassic feldspar, and carbonate inclusions, which are dominated by calcite. Heating and homogenization of the inclusions show that the potassic lamprophyres crystallized from a heterogeneous magma, with consisted of mixing mafic sodic and potassic alkaline magmas enriched in a carbonatite component. The composition of the magmas was close to nepheline and leucite melanephelinite. The minerals crystallized at 1150–1090°C from the sodic melts and at 1200–1250°C from the potassic ones. The sodic mafic melts were richer in Fe than the potassic ones, were the richest in Al, Mn, SO3, Cl, and H2O and poorer in Ti and P. The potassic mafic melts were not lamproitic, as follows from the presence of albite in the crystallized primary potassic melt inclusions. The diopside, the first mineral to crystallize in the rock, started to crystallize in the magmatic chamber from sodic mafic melt and ended to crystallize from mixed sodic–potassic melts. The potassic mafic melts were multiply replenished in the chamber in relation to tectonic motions. The ascent of the melts to the surface and rapidly varying P–T parameters of the magma were favorable for multiple separations of carbonatite melts from the alkaline mafic ones and their mixing and mingling.  相似文献   

20.
Experimental constraints on the origin and evolution of mildly alkalic basalts from the Kerguelen Archipelago, Southeast Indian Ocean     
James S. Scoates  Mauro Lo Cascio  Dominique Weis  Donald H. Lindsley 《Contributions to Mineralogy and Petrology》2006,151(5):582-599
This experimental study examines the role of clinopyroxene fractionation on major element trends and alkalinity variations in mildly alkalic basalts from the Kerguelen Archipelago, Southeast Indian Ocean. Equilibrium crystallization experiments were carried out on a natural basalt (MgO=5 wt.%, alkalinity index=0.10) over a range of pressures (0–1.43 GPa) and water contents (nominally dry to hydrous, 1.2 wt.% H2O) under relatively oxidizing conditions (Δlog FMQ=+1 to +2) at 0 GPa and relatively reducing conditions (Δlog FMQ=0 to –2) at all higher pressures. The hydrous experiments at 0.93 GPa closely reproduce most of the compositional variations in the 24–25 Ma mildly alkalic lavas from the archipelago, which supports a major role for high-Al clinopyroxene fractionation (5–9 wt.% Al2O3) at pressures corresponding to the base of the Northern Kerguelen Plateau (15–20 km). However, clinopyroxene fractionation at depth fails to produce important changes in the alkalinity of the residual melts. The transition from tholeiitic to mildly alkalic basalts on the Kerguelen Archipelago thus reflects primarily changes in melting conditions (lower extents of partial melting at higher pressures), which is related to crustal and lithospheric thickening as distance from the Southeast Indian Ridge increased over time from 43 to 24 Ma.  相似文献   

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1.
L.I. Panina  L.M. Usoltseva 《Lithos》2008,103(3-4):431-444
To find out the reasons responsible for the diversity of igneous rocks forming the alkaline-ultrabasic carbonatite Krestovskiy massif (the Maimecha–Kotui province, Russia) we have studied melt inclusions in clinopyroxene of trachydolerites, porphyric melanephelinites, and tholeiites. It was established that the homogenization temperatures of inclusions in these rocks are rather close: 1140–1180 °C, 1190–1230 °C, and 1150–1210 °C, respectively. Compositions of melt inclusions in clinopyroxenes from different rocks are significantly different. The chemical composition of clinopyroxene of trachydolerites corresponds to that of trachybasalts and their derivatives. The inclusions are enriched in Sr, Ba, P, and S and their total sum of alkalies (at K ≥ Na) is never less than 5–6 wt.%. Inclusions from the rims of clinopyroxene phenocrysts in porphyric melanephelinites are similar in composition also to inclusions in trachydolerites. But in the cores of clinopyroxene phenocrysts the composition of inclusions corresponds to nephelinite melt. The composition of some melt inclusions in the intermediate and cores zones of clinopyroxene from porphyric melanephelinite has high SiO2 (53–55 wt.%), MgO (8–9 wt.%) and a low (1–2 wt.%) total sum of alkalies (at Na ≥ K) and is depleted in Al2O3 (6–7 wt.%), which is similar to the composition of basaltic komatiites. The composition of inclusions in tholeiites is also basic, highly magnesian, and low-alkaline, Sr and Ba are rare to absent. Compared to the inclusions of basaltic komatiite composition, the inclusions in tholeiites are enriched in Al and depleted in Ca, Ti, and P. The melts trapped in clinopyroxenes from different rocks contain low (0.014–0.018 wt.%) water but they are enriched in F: from 0.37 wt.% in nephelinite melts to 0.1–0.06 wt.% in tholeiite and basaltic komatiite melts. Inclusions in all the rocks under study, host clinopyroxene, and the rocks themselves are significantly enriched in incompatible elements (1–2 orders of magnitude relative to the mantle norm). In tholeiites, the partitioning of these elements is rather uniform, while in trachydolerites and especially in melanephelinites it is contrasting with a drastic depletion in HREE relative to LREE, MREE, and HFSE. A conclusion is made that the Krestovskiy massif was formed by no less than three mantle-derived magmas: melanephelinite, tholeiite and basaltic komatiite. Magmas were generated in different magma sources at different depths with various degrees of enrichment in incompatible elements. These magmas were, most likely, dominated by melanephelinite magma. In intermediate chambers this magma differentiated to form derivative melts of nephelinite, trachydolerite–trachyandesite–trachyte compositions. Komatiite-basalt melts were, most likely, derivatives of primitive meimechite magmas.  相似文献   

2.
Peralkaline acid liquids: A petrological study   总被引:1,自引:0,他引:1  
Electron-microprobe analyses of the feldspars and associated ferromagnesian minerals in the peralkaline volcanics, comendites and pantellerites, are presented together with new data on the major and trace-elements of the rocks and residual glasses. The feldspar phenocrysts in the pantellerites span a narrower range (Or33–Or39) than those of the comendites (Or30–Or46); both sets show only limited increase in Or outwards, and the zoning is greatest in quartz-bearing assemblages. The feldspar microlites in the residual glasses are invariably more potassic (2–4% Or) than their associated phenocrysts. In pantellerites the feldspars become more potassic as the residual liquids become more sodic; thus the most potassic feldspar is found in the most sodic (and peralkaline) pantellerite.Of the ferromagnesian phenocrysts, aenigmatite is the most ubiquitous and is commonly associated with hedenbergite±fayalite, or ferrorichterite; in the later stages of crystallization (groundmass), it is associated with acmite, arfvedsonite and tuhualite. Aside from slight variation in Ti/Fe+Ti ratio, aenigmatite is virtually constant in composition. The pyroxenes from the different assemblages have zones which together almost span the range acmitehedenbergite. Both ferrorichterite and arfvedsonite incorporate F but not Cl, and are slightly potassic. Tuhualite exists as two varieties; one blue and potassic, the other violet and sodic; both varieties reject halogens. Using (estimated) free-energy data, a field in fo2, T space is postulated in which Fe-Ti oxides are absent; their place is taken by pyroxene and aenigmatite. The no-oxide field will be intercepted by a cooling liquid in which peralkalinity is increasing and in which fo2 is near but above the FMQ buffer.The characteristic pattern of trace-elements in peralkaline volcanics (e.g., high Nb, Ta, Zr, Mo, Zn, Cd, R.E, etc; low Sr, Ba, Mg) are considered to be as much evidence for the peralkaline (salic) condition as of the genetic process. Several lines of evidence suggest that at liquidus temperatures, peralkaline rhyolites are essentially anhydrous.  相似文献   

3.
The Central African Belt in the Nkambe area, northwestern Cameroon represents a collisional zone between the Saharan metacraton and the Congo craton during the Pan-African orogeny, and exposes a variety of granitoids including foliated and massive biotite monzogranites in syn- and post-kinematic settings. Foliated and massive biotite monzogranites have almost identical high-K calc-alkaline compositions, with 73–67 wt.% SiO2, 17–13 wt.% Al2O3, 2.1–0.9 wt.% CaO, 4.4–2.7 wt.% Na2O and 6.3–4.4 wt.% K2O. High concentrations of Rb (264–96 ppm), Sr (976–117 ppm), Ba (3680–490 ppm) and Zr (494–99 ppm), with low concentrations of Y (mostly< 20 ppm with a range 54–6) and Nb (up to 24 ppm) suggest that the monzogranites intruded in collisional and post-collisional settings. The Sr/Y ratio ranges from 25 to 89. K, Rb and Ba resided in a single major phase such as K-feldspar in the source. Garnet was present in the source and remained as restite at the site of magma generation. This high K2O and Sr/Y granitic magma was generated by partial melting of a granitic protolith under high-pressure and H2O undersaturated conditions where garnet coexists with K-feldspar, albitic plagioclase. CHIME (chemical Th–U-total Pb isochron method) dating of zircon yields ages of 569 ± 12–558 ± 24 Ma for the foliated biotite monzogranite and 533 ± 12–524 ± 28 Ma for the massive biotite monzogranite indicating that the collision forming the Central African Belt continued in to Ediacaran (ca 560 Ma).  相似文献   

4.
Mica kimberlite and alkali picrite were identified in the northwestern Urik-Iya Graben of the eastern Sayan region. Typomorphism of Cr-diopside and high-Cr (up to 55.22 wt % Cr2O3) spinel from kimberlite of the Bushkanai dike indicate that the melt was generated in the mantle, composed of spinel peridotite. The high content of Cr-spinel (45–55 wt % Cr2O3) microlites in the groundmass of kimberlite and small amounts of ulvospinel and titanomagnetite in the absence of perovskite testifies to the diamond potential of this kimberlite. Picroilmenite, manganoilmenite with an anomalously high MnO content (11.37–17.78 wt %), and barium titanate with (wt %) 62.21 TiO2, 0.61 Cr2O3, 15.89 FeO, 4.05 MnO, 1.71 CaO, and 11.13 BaO close in composition to a new mineral species from the Murun pluton were identified in the groundmass for the first time. Kimberlite from the Bushkanai dike belongs to the Zolotitsa low-Ti geochemical type of kimberlites derived from the slightly enriched lithospheric mantle EM1. The distribution of trace elements, including REE, in picrite from the same dike corresponds to the slightly depleted asthenospheric mantle. Different mantle sources of kimberlite and picrite from the same dike indicate that these rocks are related to independent melts rather than to products of fractionation of a common parental alkaline ultramafic magma.  相似文献   

5.
Systematic geochronologic, geochemical, and Nd isotopic analyses were carried out for an early Paleoproterozoic high-K intrusive complex exposed in southwestern Tarim, NW China. The results provide a better understanding of the Paleoproterozoic tectonic evolution of the Tarim Block. Zircon U–Pb age dating indicates two Paleoproterozoic magmatic episodes occurring at ca. 2.41 Ga and ca. 2.34 Ga respectively, which were followed by a ca. 1.9 Ga metamorphic event. The 2.41 Ga granodiorite–adamellite suite shares characteristics of late to post-orogenic metaluminous A-type granites in its high alkalinity (Na2O + K2O = 7.6–9.3%), total REE (410–788 ppm), Zr (370–660 ppm), and Y (21.7–58.4 ppm) contents. εNd(t) values for the suite range from − 3.22 to − 4.71 and accordingly the Nd modal ages (T2DM) vary between 3.05 Ga and 3.17 Ga. Based on geochemical data, the 2.34 Ga suite can be subdivided into two sub-suites, namely A-type and S-type. However, both types have comparable Nd isotope compositions (εNd(t) ≈ − 0.41 to − 2.08) and similar narrow T2DM ranges (2.76–2.91 Ga).Geochemical and Nd isotopic data for the high-K intrusive complex, in conjunction with the regional geological setting, suggest that both the 2.41 Ga suite and the 2.34 Ga A-type sub-suite might have been produced by partial melting of the Archean mafic crust in a continental rift environment. The S-type sub-suite is thought to have formed by partial melting of felsic pelites and/or metagreywackes recycled from Archean crust (TTG?). Gabbro enclaves with positive εNd(t) value (2.15) have been found to be intermingling within the 2.34 Ga suite; ca. 2.34–2.36 Ga gabbroic dykes and adamellites have previously been documented in eastern Tarim. These observations indicate that the high-K intrusions may reflect the emergence of depleted mantle upwelling beneath the Tarim Block at that time. We suggest a three-stages model for the Precambrian crustal evolution in the Tarim Block: (1) the formation of proto-crust (TTG) by ca. 2.5 Ga, (2) episodes of felsic magmatism possibly occurring in continental rift environments at ca. 2.41 Ga and ca. 2.34–2.36 Ga, and (3) ca. 1.9 Ga metamorphism that may represent the solidification of the Precambrian basement of the Tarim Block.  相似文献   

6.
A geochemical and isotopic study was carried out for the Mesozoic Yangxin, Tieshan and Echeng granitoid batholiths in the southeastern Hubei Province, eastern China, in order to constrain their petrogenesis and tectonic setting. These granitoids dominantly consist of quartz diorite, monzonite and granite. They are characterized by SiO2 and Na2O compositions of between 54.6 and 76.6 wt.%, and 2.9 to 5.6 wt.%, respectively, enrichment in light rare earth elements (LREE) and large ion lithophile elements (LILE), and relative depletion in Y (concentrations ranging from 5.17 to 29.3 ppm) and Yb (0.34–2.83 ppm), with the majority of the granitoids being geochemically similar to high-SiO2 adakites (HSA). Their initial Nd (εNd = − 12.5 to − 6.1) and Sr ((87Sr/86Sr)i = 0.7054–0.7085) isotopic compositions, however, distinguish them from adakites produced by partial melting of subducted slab and those produced by partial melting of the lower crust of the Yangtze Craton in the Late Mesozoic. The granitoid batholiths in the southeastern Hubei Province exhibit very low MgO ranging from 0.09 to 2.19 wt.% with an average of 0.96 wt.%, and large variations in negative to positive Eu anomalies (Eu/Eu = 0.22–1.4), especially the Tieshan granites and Yangxin granite porphyry (Eu/Eu = 0.22–0.73). Geochemical and Nd–Sr isotopic data demonstrate that these granitoids originated as partial melts of an enriched mantle source that experienced significant contamination of lower crust materials and fractional crystallization during magma ascent. Late Mesozoic granitoids in the southeastern Hubei Province of the Middle–Lower Yangtze River belt were dominantly emplaced in an extensional tectonic regime, in response to basaltic underplating, which was followed by lithospheric thinning during the early Cretaceous.  相似文献   

7.
Mt. Shasta andesite and dacite lavas contain high MgO (3.5–5 wt.%), very low FeO*/MgO (1–1.5) and 60–66 wt.% SiO2. The range of major and trace element compositions of the Shasta lavas can be explained through fractional crystallization (~50–60 wt.%) with subsequent magma mixing of a parent magma that had the major element composition of an H2O-rich primitive magnesian andesite (PMA). Isotopic and trace element characteristics of the Mt. Shasta stratocone lavas are highly variable and span the same range of compositions that is found in the parental basaltic andesite and PMA lavas. This variability is inherited from compositional variations in the input contributed from melting of mantle wedge peridotite that was fluxed by a slab-derived, fluid-rich component. Evidence preserved in phenocryst assemblages indicates mixing of magmas that experienced variable amounts of fractional crystallization over a range of crustal depths from ~25 to ~4 km beneath Mt. Shasta. Major and trace element evidence is also consistent with magma mixing. Pre-eruptive crystallization extended from shallow crustal levels under degassed conditions (~4 wt.% H2O) to lower crustal depths with magmatic H2O contents of ~10–15 wt.%. Oxygen fugacity varied over 2 log units from one above to one below the Nickel-Nickel Oxide buffer. The input of buoyant H2O-rich magmas containing 10–15 wt.% H2O may have triggered magma mixing and facilitated eruption. Alternatively, vesiculation of oversaturated H2O-rich melts could also play an important role in mixing and eruption.  相似文献   

8.
9.
The Permian–Jurassic Mahanadi and Pranhita–Godavari Rifts are part of a drainage system that radiated from the Gamburtsev Subglacial Mountains in central Antarctica. From 12 samples we analysed detrital zircons for U–Pb ages, Hf-isotopes, and trace elements to determine the age, rock type and source of the host magma, and TDM model age. Clusters, in decreasing order of abundance, are (1) 820–1000 Ma, host magmas felsic granitoids with alkaline rock, (2) 1500–1700 Ma felsic granitoids, (3) 500 to 700 Ma mafic granitoids with alkaline rock, (4) 2400–2550 Ma granitoids, and (5) 1000–1200 Ma felsic and mafic granitoids, mafic rock, and alkaline rock. TDM ranges from 1.5 to 3.5 Ga. Joint paleoslope measurements and zircon ages indicate that the Eastern Ghats Mobile Belt (EGMB) and lateral belts and conjugate Antarctica are potential provenances. Zircons from the Gondwana Rifts differ from those in other Gondwanaland sandstones in their predominant 820–1000 Ma and 1500–1700 Ma ages (from the EGMB and conjugate Rayner–MacRobertson Belt) that dilute the 500–700 Ma (Pan-Gondwanaland) ages. The 1000–1200 Ma zircons reflect the assembly of Rodinia, the 500–700 Ma ones that of Gondwanaland; the other ages reflect collisions in the region.  相似文献   

10.
Jun-Hong Zhao  Mei-Fu Zhou 《Lithos》2008,104(1-4):231-248
Numerous Neoproterozoic felsic and mafic–ultramafic intrusions occur in the Hannan region at the northern margin of the Yangtze Block. Among these, the Wudumen and Erliba plutons consist of granodiorites and have SHRIMP zircon U–Pb ages of  735 Ma. The rocks have high K2O (0.8–3.6 wt.%) and Na2O (4.4–6.4 wt.%) and low MgO (0.4–1.7 wt.%). They also have high Sr/Y (32–209) and (La/Yb)n ratios (4.4–38.6). Their εNd values range from − 0.41 to − 0.92 and zircon initial 176Hf/177Hf ratios from 0.282353 to 0.282581. These geochemical features are similar to those of adakitic rocks produced by partial melting of a thickened lower crust. Our new analytical results, combined with the occurrence of voluminous arc-related mafic–ultramafic intrusions emplaced before 740 Ma, lead us to propose that the crustal evolution in the northern margin of the Yangtze Block during Neoproterozoic involved: (1) rapid crustal growth and thickening by underplating of mafic magmas from the mantle which was modified by materials coming from the subducting oceanic slab from  1.0 to  0.74 Ga, and (2) partial melting of the thickened lower crust due to a thermal anomaly induced by upwelling of asthenosphere through an oceanic slab window, producing the  735 Ma adakitic Wudumen and Erliba plutons. Our model suggests that the crustal thickness was more than 50 km at the northern margin of the Yangtze Block at  735 Ma, and rule out the possibility of a mantle plume impact causing the > 735 Ma magmatism in the region.  相似文献   

11.
Melt inclusions in olivine and plagioclase phenocrysts from rocks (magnesian basalt, basaltic andesite, andesite, ignimbrite, and dacite) of various age from the Gorely volcanic center, southern Kamchatka, were studying by means of their homogenization and by analyzing the glasses in 100 melt inclusions on an electron microprobe and 24 inclusions on an ion probe. The SiO2 concentrations of the melts vary within a broad range of 45–74 wt %, as also are the concentrations of other major components. According to their SiO2, Na2O, K2O, TiO2, and P2O5 concentrations, the melts are classified into seven groups. The mafic melts (45–53 wt % SiO2) comprise the following varieties: potassic (on average 4.2 wt % K2O, 1.7 wt % Na2O, 1.0 wt % TiO2, and 0.20 wt % P2O5), sodic (3.2% Na2O, 1.1% K2O, 1.1% TiO2, and 0.40% P2O5), and titaniferous with high P2O5 concentrations (2.2% TiO2, 1.1% P2O5, 3.8% Na2O, and 3.0% K2O). The melts of intermediate composition (53–64% SiO2) also include potassic (5.6% K2O, 3.4% Na2O, 1.0% TiO2, and 0.4% P2O5) and sodic (4.3% Na2O, 2.8% K2O, 1.3% TiO2, and 0.4% P2O5) varieties. The acid melts (64–74% SiO2) are either potassic (4.5% K2O, 3.6% Na2O, 0.7% TiO2, and 0.15% P2O5) or sodic (4.5% Na2O, 3.1% K2O, 0.7% TiO2, and 0.13% P2O5). A distinctive feature of the Gorely volcanic center is the pervasive occurrence of K-rich compositions throughout the whole compositional range (silicity) of the melts. Melt inclusions of various types were sometimes found not only in a single sample but also in the same phenocrysts. The sodic and potassic types of the melts contain different Cl and F concentrations: the sodic melts are richer in Cl, whereas the potassic melts are enriched in F. We are the first to discover potassic melts with very high F concentrations (up to 2.7 wt %, 1.19 wt % on average, 17 analyses) in the Kuriles and Kamchatka. The average F concentration in the sodic melts is 0.16 wt % (37 analyses). The melts are distinguished for their richness in various groups of trace elements: LILE, REE (particularly HREE), and HFSE (except Nb). All of the melts share certain geochemical features. The concentrations of elements systematically increase from the mafic to acid melts (except only for the Sr and Eu concentrations, because of active plagioclase fractionation, and Ti, an element contained in ore minerals). The paper presents a review of literature data on volcanic rocks in the Kurile-Kamchatka area in which melt inclusions with high K2O concentrations (K2O/Na2O > 1) were found. K-rich melts are proved to be extremely widespread in the area and were found on such volcanoes as Avachinskii, Bezymyannyi, Bol’shoi Semyachek, Dikii Greben’, Karymskii, Kekuknaiskii, Kudryavyi, and Shiveluch and in the Valaginskii and Tumrok Ranges.  相似文献   

12.
Glasses have been analysed from six mantle-derived xenoliths (5 orthopyroxene and/or olivine-rich, 1 clinopyroxene-rich) from the Quaternary volcanics S.E. of Gees, West Eifel, Germany. The glasses in these xenoliths occur as pools surrounding and embaying spinels, as inclusions in spinels, as veins and stringers within phlogopiterich veins, and as jackets partially surrounding some of the xenoliths. Glasses analysed are felsic and characterised by low to intermediate SiO2 (40–62 wt.%), variable CaO (1–11 wt.%) and MgO (1–4 wt.%), high Al2O3 (14–21 wt.%), and up to 11 wt.% Na2O + K2O. The jacket glasses have the lowest SiO2, highest CaO and MgO. Variations in all of the glass compositions are similar and imply a unifying factor or process in their formation. Glass as pools and stringers within veins of phlogopite forms part of the same trends shown by all the glasses when plotted on bivariate (oxide vs SiO2) diagrams but can be distinguished from glass surrounding and enclosed by spinels. Glasses occurring as jackets are similar in composition to those in pools and veinlets associated with phlogopite but are of quite different composition to the glasses found within the xenoliths that they partially enclose. The occurrence and chemistry of the glasses do not support such glasses as representing original or differentiated magma trapped during formation of the xenolithic assemblages. The chemistry of the glasses also makes it unlikely that they were produced by dissociation of phlogopite during ascent of the xenoliths. The most likely origin for the glasses is that they represent volatile-rich melts which migrated through upper mantle material. These melts are likely to be responsible for the heterogeneous nature of the mantle underlying this part of the West Eifel region.  相似文献   

13.
Huaiwei Ni  Youxue Zhang   《Chemical Geology》2008,250(1-4):68-78
Water diffusion in silicate melts is important for understanding bubble growth in magma, magma degassing and eruption dynamics of volcanos. Previous studies have made significant progress on water diffusion in silicate melts, especially rhyolitic melt. However, the pressure dependence of H2O diffusion is not constrained satisfactorily. We investigated H2O diffusion in rhyolitic melt at 0.95–1.9 GPa and 407–1629 °C, and 0.2–5.2 wt.% total water (H2Ot) content with the diffusion-couple method in a piston-cylinder apparatus. Compared to previous data at 0.1–500 MPa, H2O diffusivity is smaller at higher pressures, indicating a negative pressure effect. This pressure effect is more pronounced at low temperatures. Assuming H2O diffusion in rhyolitic melt is controlled by the mobility of molecular H2O (H2Om), the diffusivity of H2Om (DH2Om) at H2Ot ≤ 7.7 wt.%, 403–1629 °C, and ≤ 1.9 GPa is given by
DH2Om=D0exp(aX),
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