Palaeoenvironmental Reconstruction of the Early to Middle Miocene Sequence in West Central Sinai,Egypt, as Revealed from Fossil Diatoms     

Abdelfattah A. ZALAT 《《地质学报》英文版》2018,92(1):354-366

A detailed analysis of the diatoms from the sedimentary sequence exposed in Abu Qada basin, west central Sinai, was used to determine the palaeoenvironmental changes during the Lower to Middle Miocene. A total of 85 diatom species and varieties belonging to 37 genera were identified from 154 samples collected throughout the stratigraphic succession. The lithological characters of the studied samples varied between sandstone, silty interbeds, sandy shales, shales, and terminated with anhydrite and limestones. These rock units are included in two lithostratigraphic formations (Rudies and Kareem), which are separated by a marked unconformity. The distribution and preservation of fossil diatoms in the sedimentary record are examined with the aim of outlining the temporal and spatial variation in the composition of the diatom assemblages, in order to estimate the changes in depositional environments during the Lower to Middle Miocene. The distributional pattern of the recorded diatom taxa distinguished four diatom eco-zones. The environment of each eco-zone is deduced and a proposed paleobathymetric change and depositional history of the Miocene sediments in the studied area are given.  相似文献   

Geochemistry and Petrogenesis of Intracontinental Basaltic Volcanism on the Northwest Arabian Plate,Gaziantep Basin,Southeast Anatolia,Turkey     

Sevcan KüRüM  Abdurrahman B?LüCü  Melek URAL 《《地质学报》英文版》2018,92(2):519-535

Volcanism along the northwest boundary of the Arabian Plate found in the Gaziantep Basin, southeast Turkey, is of Miocene age and is of alkaline and calc-alkaline basic composition. The rare earth element data for both compositional series indicates spinel–peridotite source areas. The rare earth and trace elements of the alkaline lavas originate from a highly primitive and slightly contaminated asthenospheric mantle; those of the calc-alkaline lavas originate from a highly heterogeneous, asthenospheric, and lithospheric mantle source. Partial melting and magmatic differentiation processes played a role in the formation of the petrological features of these volcanics. These rocks form two groups on the basis of their ~(87) Sr/~(86) Sr and ~(143) Nd/~(144) Nd isotopic compositions in addition to their classifications based on their chemical compositions(alkaline and calc-alkaline). These isotopic differences indicate a dissimilar parental magma. Therefore, high Nd isotope samples imply a previously formed and highly primitive mantle whereas low Nd isotope samples may indicate comparable partial melting of an enriched heterogeneous shallow mantle. Other isotopic changes that do not conform to the chemical features of these lavas are partly related to the various tectonic events of the region, such as the Dead Sea Fault System and the Bitlis Suture Zone.  相似文献   

The accuracy of standard enthalpies and entropies for phases of petrological interest derived from density-functional calculations     

Artur?BenisekEmail authorView author&#;s OrcID profile  Edgar?Dachs 《Contributions to Mineralogy and Petrology》2018,173(11):90

The internal energies and entropies of 21 well-known minerals were calculated using the density functional theory (DFT), viz. kyanite, sillimanite, andalusite, albite, microcline, forsterite, fayalite, diopside, jadeite, hedenbergite, pyrope, grossular, talc, pyrophyllite, phlogopite, annite, muscovite, brucite, portlandite, tremolite, and CaTiO₃–perovskite. These thermodynamic quantities were then transformed into standard enthalpies of formation from the elements and standard entropies enabling a direct comparison with tabulated values. The deviations from reference enthalpy and entropy values are in the order of several kJ/mol and several J/mol/K, respectively, from which the former is more relevant. In the case of phase transitions, the DFT-computed thermodynamic data of involved phases turned out to be accurate and using them in phase diagram calculations yields reasonable results. This is shown for the Al₂SiO₅ polymorphs. The DFT-based phase boundaries are comparable to those derived from internally consistent thermodynamic data sets. They even suggest an improvement, because they agree with petrological observations concerning the coexistence of kyanite?+?quartz?+?corundum in high-grade metamorphic rocks, which are not reproduced correctly using internally consistent data sets. The DFT-derived thermodynamic data are also accurate enough for computing the P–T positions of reactions that are characterized by relatively large reaction enthalpies (>?100 kJ/mol), i.e., dehydration reactions. For reactions with small reaction enthalpies (a few kJ/mol), the DFT errors are too large. They, however, are still far better than enthalpy and entropy values obtained from estimation methods.  相似文献   

Three Types of Apatite in Norilsk Sulfide Ores     

A. A. Serova  E. M. Spiridonov 《Geochemistry International》2018,56(5):474-483

Apatite is a concentrator of F and Cl, which play a significant role in the formation of minerals of platinum-group elements of pneumatolitic origin. There are three apatite generations in Norilsk magmatic sulfide ores. Apatite I occurs in sulfide bodies and rims of fluid alteration above sulfide droplets in disseminated ores. Its composition evolved from hydroxyl-chlorapatite to chlorapatite. Apatite I associates with Tiрbiotite, titanomagnetite, ilmenite with baddeleyite lamellae, anhydrite, Ti-poor kaersutite, Cl-bearing hastingsite and edenite, djerfisherite, bartonite, and minerals of the Pt and Au groups. Apatite I contains up to 2.3 wt % lanthanides, primarily Ce, La, and Nd. Apatite I is overgrown and replaced by apatite II, the composition of which evolved from hydroxyl-chlor-fluorapatite to fluorapatite. Apatite II often occurs also as individual crystals in massive sulfides and contains up to 0.9 wt % lanthanides. The pneumatolitic chlorapatite and fluorapatite contain ~0.5 wt % SiO₂. The composition of apatite indicates discrete evolution of fluids released during the crystallization of Norilsk sulfide melts: from water–chloride to chloride at the first state, and from water–chlorite–fluoride to essentially fluoride at the second stage. The lanthanides released during the replacement of chlorapatite I by fluorapatite II were probably incorporated in pneumatolitic zoned orthite-(Ce). In the areas affected by prehnite–pumpellyite metamorphism, apatite I and apatite II within metamorphosed sulfide ores are partly or completely replaced by apatite III, which varies in composition from hydroxyl-chlorapatite to hydroxylapatite poor in fluorine and lanthanides. The lanthanides released during the replacement of apatite I and II by metamorphic hydroxylapatite III were probably incorporated in metamorphic unzoned orthite-(Ce).  相似文献   

Composition,Structure, and Conditions of Formation of Fluorine-Bearing Sodalite: Experimental Evidence     

E. N. Gramenitskii  A. R. Kotel’nikov  T. I. Shchekina  O. V. Yakubovich  V. N. Devyatova  E. S. Zubkov  N. I. Suk  M. F. Vigasina  Z. A. Kotel’nikova 《Geochemistry International》2018,56(6):521-534

Fluoro-sodalite was synthesized for the first time at temperatures of 400–800°C and H₂O pressures of 1–2 kbar in the Si–Al–Na–H–O–F system. X-ray diffraction and infrared spectroscopic investigations showed that fluorine is incorporated in the sodalite structure as anionic octahedral groups, [AlF₆]^3–, the number of which can vary from 0 to 1. Correspondingly, the end-members of the F-sodalite series are Na₇(H₂O)₈[Si₅Al₇O₂₄] and Na₈(AlF₆)(H₂O)₄[Si₇Al₅O₂₄]. Depending on the composition of the system, F-sodalite associates at 500–650°C with nepheline, albite, cryolite, and villiaumite, which are joined by analcime below 500°C and aluminosilicate melt above 650°C. Fluorine-bearing sulfate–chlorine-sodalite was found for the first time in a pegmatite sample from the Lovozero massif. The highest fraction of the fluorine end-member in natural sodalite is 0.2. The incorporation of F into the sodalite structure requires much more energy compared with Cl^– and SO ₄ ^2- , because it is accompanied by a structural rearrangement and a transition from tetrahedral Al to octahedral Al.  相似文献   

Petrology and Rare Earth Elements Mineral Chemistry of Chadegan Metabasites (Sanandaj-Sirjan Zone,Iran): Evidence for Eclogite-Facies Metamorphism during Neotethyan Subduction     

K. Akbari  S. M. Tabatabaei Manesh  O. V. Parfenova 《Geochemistry International》2018,56(7):670-687

The metabasites of Chadegan, including eclogite, garnet amphibolite and amphibolite, are forming a part of Sanandaj–Sirjan Zone. These rocks have formed during the subduction of the Neo–Tethys ocean crust under Iranian plate. This subduction resulted in a subduction metamorphism under high pressuremedium temperature of eclogite and amphibolites facies condition. Then the metamorphic rocks were exhumed during the continental collision between the Afro–Arabian continent and the Iranian microcontinent. In the metabasite rocks, with typical MORB composition, garnet preserved a compositional zoning occurred during metamorphism. The magnesium (X_Mg) gradually increases from core to rim of garnets, while the manganese (X_Mn) decreases towards the rim. Chondrite–normalized Rare Earth Element patterns for these garnets exhibit core–to–rim increases in Light Rare Earth Elements. The chondrite–normalized REE patterns of garnets, amphiboles and pyroxenes display positive trend from LREEs to Heavy Rare Earth Elements (especially in garnet), which suggests the role of these minerals as the major controller of HREE distribution. The geochemical features show that the studied eclogite and associated rocks have a MORB origin, and probably formed in a deep–seated subduction channel environment. The geothermometry estimation yields average pressure of ~22 kbar and temperature of 470–520°C for eclogite fomation. The thermobarometry results gave T = 650–700°C and P ≈ 10–11 kbar for amphibolite facies.  相似文献   

Evolutionary Processes in Anthropogenic Biogeochemical Provinces     

T. I. Moiseenko 《Geochemistry International》2018,56(10):982-991

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Olivine in ultramafic lamprophyres: chemistry,crystallisation, and melt sources of Siberian Pre- and post-trap aillikites     

A.?A.?NosovaEmail authorView author&#;s OrcID profile  L.?V.?Sazonova  A.?V.?Kargin  M.?D.?Smirnova  A.?V.?Lapin  V.?D.?Shcherbakov 《Contributions to Mineralogy and Petrology》2018,173(7):55

We studied olivines from the Devonian pre-trap (the Ilbokich occurrence) and the Triassic post-trap (the Chadobets occurrence) carbonate-rich ultramafic lamprophyres (UMLs) in the southwestern portion of the Siberian craton. On the basis of detailed investigations of major, minor, and trace-element distributions, we have reconstructed the main processes that control the origins of these olivines. These include fractional crystallisation from melt, assimilation, and fractional crystallisation processes with orthopyroxene assimilation, melt-reaction diffusive re-equilibration, alkali enrichment, and CO₂ degassing of the melt. Furthermore, we inferred the composition of the sources of the primary UML melt and their possible correlations with proto-kimberlitic melts, as well as the influence of the Triassic Siberian plume on the composition of the lithospheric mantle. The main differences between olivines from the Ilbokich and the Chadobets aillikites were that the olivines from the former had more magnesium-rich cores (Mg# = 89.2?±?0.2), had Mg- and Cr-rich transition zones (Mg# = 89.7?±?0.2 and 300–500 ppm Cr), had lower Ni (up to 3100 ppm) and Li (1.4–1.5 ppm), and had higher B (0.8–2.6 ppm) contents, all at higher Fo values (90–86), relative to the olivines from the latter (Mg# = 88–75; 200–300 ppm Cr; up to 3400 ppm Ni; 1.4–2.4 ppm Li; 0.4–2.2 ppm B). The Siberian aillikite sources contained a significant amount of metasomatic material. Phlogopite-rich MARID-type veins provided the likely metasomatic component in the pre-trap Devonian Ilbokich aillikite source, whereas the Triassic Chadobets aillikitic post-trap melts were derived from a source with a significant carbonate component. A comparison of UML olivines with olivines from the pre-trap and post-trap Siberian kimberlites shows a striking similarity. This suggests that the carbonate component in the aillikitic source could have been produced by evolved kimberlite melts. The differences in the lithospheric metasomatic component that contributed to pre-trap and post-trap aillikitic melts can be interpreted as reflections of the thermal impact of the Siberian Traps, which reduced phlogopite-bearing metasomes within the southwestern Siberian sub-continental lithospheric mantle.  相似文献   

Apatite-hosted melt inclusions from the Panzhihua gabbroic-layered intrusion associated with a giant Fe–Ti oxide deposit in SW China: insights for magma unmixing within a crystal mush     

Kun?Wang  Christina?Yan?WangEmail author  Zhong-Yuan?RenEmail author 《Contributions to Mineralogy and Petrology》2018,173(7):59

The ～?2-km-thick Panzhihua gabbroic-layered intrusion in SW China is unusual because it hosts a giant Fe–Ti oxide deposit in its lower zone. The deposit consists of laterally extensive net-textured and massive Fe–Ti oxide ore layers, the thickest of which is ～?60 m. To examine the magmatic processes that resulted in the Fe enrichment of parental high-Ti basaltic magma and the formation of thick, Fe–Ti oxide ore layers, we carried out a detailed study of melt inclusions in apatite from a ～?500-m-thick profile of apatite-bearing leucogabbro in the middle zone of the intrusion. The apatite-hosted melt inclusions are light to dark brown in color and appear as polygonal, rounded, oval and negative crystal shapes, which range from ～?5 to ～?50 µm in width and from ～?5 to ～?100 µm in length. They have highly variable compositions and show a large and continuous range of SiO₂ and FeO_t with contrasting end-members; one end-member being Fe-rich and Si-poor (40.2 wt% FeO_t and 17.7 wt% SiO₂) and the other being Si-rich and Fe-poor (74.0 wt% SiO₂ and 1.20 wt% FeO_t). This range in composition may be attributed to entrapment of the melt inclusions over a range of temperature and may reflect the presence of µm-scale and immiscible Fe-rich and Si-rich components in different proportions. Simulating results for the motion of Si-rich droplets within a crystal mush indicate that Si-rich droplets would be separated from Fe-rich melt and migrate upward due to density differences in the interstitial liquid when the magma unmixed. Migration of the Si-rich, immiscible liquid component from the interstitial liquid caused the remaining Fe-rich melt in the lower part to react with plagioclase primocrysts (An_59–60), as evidenced by fine-grained lamellar intergrowth of An-rich plagioclase (An_79–84)?+?clinopyroxene in the oxide gabbro of the lower zone. Therefore, magma unmixing within a crystal mush, combined with gravitationally driven loss of the Si-rich component, resulted in the formation of Fe-rich, melagabbro and major Fe–Ti oxide ores in the lower part and Si-rich, leucogabbro in the upper part of the intrusion.  相似文献   

Formation by silicate–fluoride + phosphate melt immiscibility of REE-rich globular segregations within aplite dikes     

Charles?R.?SternEmail author  Julien?M.?Allaz  Markus?B.?Raschke  G.?Lang?Farmer  M.?Alexandra?Skewes  Jeremy?T.?Ross 《Contributions to Mineralogy and Petrology》2018,173(8):65

Aplite dikes intruding the Proterozoic 1.42(±?3) Ga Longs Peak-St. Vrain Silver Plume-type peraluminous granite near Jamestown, Colorado, contain F, P, and rare earth element (REE)-rich globular segregations, with 40–46% REE, 3.7–4.8 wt% P₂O₅, and 5–8 wt% F. A combination of textural features and geochemical data suggest that the aplite and REE-rich globular segregations co-existed as two co-genetic liquids prior to their crystallization, and we propose that they are formed by silicate–fluoride?+?phosphate (+?S?+?CO₂) melt immiscibility following ascent, cooling, and decompression of what was initially a single homogeneous magma that intruded the granite. The REE distribution coefficients between the silica-rich aplites and REE-rich segregations are in good agreement with experimentally determined distribution coefficients for immiscible silicate–fluoride?+?phosphate melts. Although monazite-(Ce) and uraninite U–Th–Pb microprobe ages for the segregations yield 1.420(±?25) and 1.442(±?8) Ga, respectively, thus suggesting a co-genetic relationship with their host granite, ε_Nd1.42Ga values for the granites and related granitic pegmatites range from ??3.3 to ??4.7 (average ??3.9), and differ from the values for both the aplites and REE-rich segregations, which range from ??1.0 to ??2.2 (average ??1.6). Furthermore, the granites and pegmatites have (La/Yb)_N <50 with significant negative Eu anomalies, which contrast with higher (La/Yb)_N >100 and absence of an Eu anomaly in both the aplites and segregations. These data are consistent with the aplite dikes and the REE-rich segregations they contain being co-genetic, but derived from a source different from that of the granite. The higher ε_Nd1.42Ga values for the aplites and REE-rich segregations suggest that the magma from which they separated had a more mafic and deeper, dryer and hotter source in the lower crust or upper mantle compared to the quartzo-feldspathic upper crustal source proposed for the Longs Peak-St. Vrain granite.  相似文献