Some pyrrhotite-chalcopyrite-bearing amphibole megacrysts (including pyroxene megacrysts) were discovered in Mesozoic augite diorite-porphyrite at Caoshan in Tongling area, Anhui Province. The amphibole megacrysts, belonging mainly to pargasite and magnesiohastingsite, are characteristic of the amphibole composition derived from mantle and crystallized in lower crust. In general, the aggregates of pyrrhotite-chalcopyrite take the shapes of cylinder and sphere. Three occurrences have been recognized in the amphibole megacrysts: parallel linear, bunchy and scattered. The unique cylinder-like shape of the aggregates and remarkable Ni-poor sulfides in Caoshan are distinctively different from the spherical Ni-rich sulfides in pyroxene megacrysts and any other kinds of megacrysts. In terms of composition, the amphibole megacrysts and their sulfides in Caoshan are similar to those in the pyroxenite xenoliths in Qilin, Guangdong Province. In terms of origin, the pyrrhotite-chalcopyrites as exsolution products resulted from the subsolidus re-equilibration of sulfide solid solution within amphibole megacrysts.amphibole megacrysts were first discovered inside and outside China. This discovery is important for the study of regional magma evolution and its associated mineralizations and ore sources as well. 相似文献
The carbon isotopic composition of CO2 inclusions trapped in minerals reflects the origin and evolution of CO2-bearing fluids and melts, and records the multiple-stages carbon geodynamic cycle, as CO2 took part in various geological processes widely. However, the practical method for determination isotope composition of individual CO2 inclusion is still lacking. Developing a microanalytical technique with spatial resolution in micrometers to precisely determinate the δ13C value of individual CO2 inclusion, will make it possible to analyze a tiny portion of a zoning mineral crystal, distinguish the differences in micro-scale, and possible to find many useful information that could not be obtained with the bulk extraction and analysis techniques. In this study, we systematically collected Raman spectra of CO2 standards with different δ13C values (?34.9 ‰ to 3.58 ‰) at 32.0 °C and from ～7.0 MPa to 120.0 MPa, and developed a new procedure to precisely determinate the δ13C value of individual CO2 inclusion. We investigated the relationship among the Raman peak intensity ratio, δ13C value, and CO2 density, and established a calibration model with high accuracy (0.5 ‰?1.5 ‰), sufficient for geological application to distinguish different source of CO2 with varying δ13CO2. As a demonstration, we measured the δ13C values and the density of CO2 inclusions in the growth zones of alkali basalt-hosted corundum megacrysts from Changle, Shandong Province. We found the significant differences of density and δ13C between the CO2 inclusions in the core of corundum and those inclusions in the outer growth zones, the δ13C value decreases from core to rim with decreasing density: δ13C values are from ?7.5 ‰ to ?9.2 ‰ for the inclusions in the core, indicating the corundum core was crystallized from mantle-derived magmas; from ?13.5 ‰ to ?18.5 ‰ for CO2 inclusions in zone 1 and from ?16.5 ‰ to –22.0 ‰ for inclusions in zone 2, indicating the outer zones of corundum grew in a low δ13C value environment, resulted from an infilling of low δ13C value fluid and/or degassing of the ascending basaltic magma. 相似文献
Garnet megacryst with a multiphase inclusion from intraplate alkali basalts of the Shavaryn Tsaram(Tariat,Mongolia)was the object of the study.This unusual aggregate consists of porous glass,Ti-rich biotite,orthopyroxene,spinel,clinopyroxene,olivine,and ilmenite.Win TWQ 2.32 thermodynamic simulation of this system revealed a few intervals of equilibrium.Pressure and temperature adjustment reflected in the paragenetic minerals of the melt pocket.The capture of already crystallised garnet megacryst was at P=0.8-1 GPa and T=1120-1160℃.Mineral crystallisation inside the melt pocket,accompanied by external inputs,occurred at P=0.75-0.95 GPa;T=790-1120℃.Symplectite assemblage formed in the garnet megacryst due to decomposition at(P=0.55-0.7 GPa;T=850-930℃).The study of the oxygen isotope content in primary garnet and biotite of the melt pocket showed that the δ18OVSMOW values are the same and correspond to that of typical mantle xenoliths.However,the chemical and microcomponent composition of the melt pocket minerals reveals a material that differs from basalts and peridotites.Thus,it has been revealed that the multiphase inclusion in the garnet megacryst formed not only on account of the garnet’s substance,but also due to the entrapped material of the Earth’s interior. 相似文献
The last stage in the formation of the Arabian Nubian Shield in Jordan was dominated by post-orogenic igneous activity of the ∼610–542 Ma Araba Suite, including a monzogabbroic stock intruding the Saramuj Conglomerate, near the southeastern corner of the Dead Sea. The geological setting, petrography, geochemistry and geothermometry of the monzogabbro and other cogenetic varieties are used to shed light on the petrogenesis of this stock and reveal its magma source. The monzogabbro, megaporphyry dikes, and scattered syenite pockets are co-magmatic and alkaline, potassic and shoshonitic in nature. REE and trace elements patterns indicate that these magmas were produced from a mantle that had been modified by subduction-related metasomatism. The parental mafic magma could have been derived by 10% partial melting of LILE-enriched phlogopite-bearing spinel lherzolite, probably lithospheric mantle, in association with post-collisional extension. Fractional crystallization of this parental magma by olivine and pyroxene gave rise to the monzogabbroic magma.The megaporphyry dikes with their giant labradorite plagioclase megacrysts represent feeders of a voluminous volcanic activity that could have lasted for about 105 years.Thermodynamic modeling applying the MELTS software indicates crystallization of this suite in the temperature range of 1184–760 °C at a pressure of 2 kbars, agreeing with olivine-pyroxene, pyroxene, and two-feldspar thermometry. The modeled mineralogy and sequence of crystallization of constituent minerals using MELTS is in remarkable agreement with the observed modal mineralogy of the monzogabbro. Furthermore, a great degree of congruity exists between the modeled and observed chemistry of the major minerals with only minor discrepancies between modeled composition of biotite and olivine. 相似文献
In situ Sr-isotope and microchemical studies were used to determine the provenance of K-feldspar megacrysts hosted in mafic alkaline potassic, ultrapotassic rocks and in differentiated rocks from two nearby volcanic apparatus in central Italy.
At Monte Cimino volcanic complex, mafic leucite-free ultrapotassic megacryst-bearing rocks of olivine latitic composition are associated with evolved latite and trachyte. Here, latites and trachytes straddle the sub-alkaline field. Age-corrected 87Sr/86Sr values (Sri) of the analysed Cimino olivine latites vary from 0.71330 and 0.71578 and strongly increase at constant Mg value. Latite and trachyte have lower Sri than olivine latites ranging between 0.71331 and 0.71361. Sri of K-feldspar megacrysts from olivine latites are between 0.71352 and 0.71397, but core and rim 87Sr/86Sr ratios within individual megacryst are indistinguishable. In all the mafic rocks, the megacrysts are not in isotopic equilibrium with the hosts. K-feldspar megacrysts from both the latite and trachyte have similar Sr-isotope compositions (Sri=0.71357–0.71401) to those in the olivine latites. However, Sri of megacryst in the trachyte vary significantly from core to rim (Sri from 0.71401 to 0.71383). As with the olivine latites, the K-feldspar megacrysts are not in isotopic equilibrium with bulk rock compositions of the latite or trachyte.
At Vico volcano, megacryst-bearing rocks are mafic leucite-free potassic rocks, mafic leucite-bearing ultrapotassic rocks and old trachytic rocks. The mafic leucite-bearing and leucite-free rocks are a tephri-phonolite and an olivine latite, respectively. A megacryst in Vico trachyte is isotopically homogeneous (Sri CORE=0.71129, RIM=0.71128) and in equilibrium with the host rock (Sri bulk ROCK=0.71125). Sri of megacryst from tephri-phonolite is clearly not in isotopic equilibrium with its host (Sri bulk ROCK=0.71158), and it increases from core (Sri=0.71063) to rim (Sri=0.71077). A megacryst in Vico olivine latite is isotopically homogeneous (Sri CORE=0.71066, RIM=0.71065), but not in equilibrium with the host rock (Sri bulk ROCK=0.71013).
The Sr isotope microdrilling technique reveals that Cimino megacrysts were crystallised in a Cimino trachytic magma and were subsequently incorporated by mixing/mingling processes in the latitic and olivine latitic melts. A model invoking the presence of a mafic sub-alkaline magma, which was mixed with the olivine latite, is proposed to justify the lack of simple geochemical mixing relation between Cimino trachytes and olivine latites. This magmatological model is able to explain the geochemical characteristics of Cimino olivine latites, otherwise ascribed to mantle heterogeneity.
The similarity of core Sri of megacrysts hosted in Vico tephri-phonolite and olivine latite suggests that the K-feldspar megacrysts are co-genetic. Isotopic equilibrium between megacryst and Vico host trachyte indicates that the trachyte is the parent of this megacryst. On the contrary, the megacrysts hosted in tephri-phonolite and olivine latite do not derive from the old trachytic magma because no diffusion process may explain the core to rim Sr isotope increase of the xenocryst hosted in the tephri-phonolite. The megacrysts hosted in the Vico mafic rocks might derive from a trachytic melt similar in composition to the old Vico trachytes. 相似文献
We present a combined Sr, Nd, Pb and Os isotope study of lavasand associated genetically related megacrysts from the Biu andJos Plateaux, northern Cameroon Volcanic Line (CVL). Comparisonof lavas and megacrysts allows us to distinguish between twocontamination paths of the primary magmas. The first is characterizedby both increasing 206Pb/204Pb (19·82–20·33)and 87Sr/86Sr (0·70290–0·70310), and decreasingNd (7·0–6·0), and involves addition of anenriched sub-continental lithospheric mantle-derived melt. Thesecond contamination path is characterized by decreasing 206Pb/204Pb(19·82–19·03), but also increasing 87Sr/86Sr(0·70290–0·70359), increasing 187Os/188Os(0·130–0·245) and decreasing Nd (7·0–4·6),and involves addition of up to 8% bulk continental crust. Isotopicsystematics of some lavas from the oceanic sector of the CVLalso imply the involvement of a continental crustal component.Assuming that the line as a whole shares a common source, wepropose that the continental signature seen in the oceanic sectorof the CVL is caused by shallow contamination, either by continent-derivedsediments or by rafted crustal blocks that became trapped inthe oceanic lithosphere during continental breakup in the Mesozoic. KEY WORDS: crustal contamination; CVL; megacrysts; ocean floor; osmium isotopes相似文献
