Petrology,geochemistry and geochronology of the Chilka Lake igneous complex,Orissa state,India

The Chilka Lake igneous complex of Orissa, the largest known anortosite massif of the Indian Shield, occurs in a catazonal environment of high-grade metamorphics of the Eastern Ghats Precambrian Orogenic Province. The syntectonic massif consists of the anorthositic Balugaon dome, leuconoritic Rambha lobe and quartz-mangeritic Kallikota cover. A completely gradational suite comprising anorthosite-leuconorite-norite-minor jotunite (the anorthositic suite) constitutes most of the complex. The subordinate of suite of acid rocks spatially associated with this is of a broad quartz-mangeritic lithology with minor granitic rocks (the acidic suite). Geochemical evolution of the complex in the sequence anorthosite-leuconorite-norite-jotunite-acidic rocks shows moderate iron enrichment in the noritic-jotunitic stage and is marked by an overall decrease in Al₂O₃, CaO, MgO, Ni/Co, Sr/Ba, K/Rb and increase in SiO₂, K₂O, V/Ni, K/Ba and Rb/Sr. Such progressive variation in geochemical parameters appears (i) essentially gradual and frequently overlapping in rock members of the intergradational anorthositic suite and (ii) rather abrupt across transition zones between the anorthositic suite and the acidic suite due to near absence of intervening intermediate lithologies. RbSr whole rock isochron studies indicate that the complex was emplaced ca. 1400 Ma ago. The initial ⁸⁷Sr/⁶⁸Sr (0.70661) implies limited hybridisation of the parent magma prior to emplacement. A critical appraisal of all the available evidence suggests that (i) the anorthositic suite of rocks form a perfectly consanguinous and comagmatic assemblage and (ii) the spatially associated acidic suite emerged through a convergence of magmatic and metasomatic processes (the latter brought about by contact anatexis of the host rocks). The complex as well as the host metamorphics are intruded by an atectonic suite of noritic dykes emplaced ca 850 Ma ago.     

A reappraisal of episodic burial metamorphism in the Andes of central Chile

The Jurassic to Miocene sequences of the central Andes, east of Santiago, reputedly show repeated cycles of episodic sub-greenschist facies, burial metamorphism that are identified by sharp breaks in metamorphic grade at major stratigraphic boundaries. This paper presents the first detailed petrochemical analysis of these low-grade metamorphic sequences by examining the progressive development of secondary minerals, reaction progress in mafic phyllosilicates, and topological variations in the low-grade assemblages as a means of testing this model. The results indicate a progressive increase from zeolite facies through to close to the onset of greenschist facies from Miocene to Jurassic rocks. Combined analysis of reaction progress in mafic phyllosilicates and petrochemical relationships of chlorite–pumpellyite–actinolite in metabasites provides no evidence for sharp metamorphic breaks at major stratigraphic boundaries. Integrating the results presented here with the most recent models of stratigraphic/tectonic development of the central Andes shows that the metamorphism took place in two episodes, and was not episodic on a 40-million-year cycle. An absence of sharp breaks in metamorphic grade in any part of the succession, as demonstrated here, shows that the original petrographic establishment of low-grade facies provided insufficient resolution of changes in metamorphic conditions to establish definitive evidence of such breaks. Accordingly, this study suggests that re-assessment of metamorphic breaks reputedly developed in other areas of the Andean Cordillera is imperative in order to resolve the questions raised here about the origin of the low-grade metamorphism.Editorial responsibility: B. Collins     

Zur chemischen Variabilität regionalmetamorph gebildeter Plagioklase,Epidote und Granate

Plagioclases, Fe-rich epidotes and garnets coexisting in metamorphic rocks of basaltoid and granitoid substrata have been analyzed by standard microprobe techniques. The results presented are based on 34000 data on plagioclases, nearly 24400 on coexisting epidotes as well as of 5000 garnet data. The chemical variations within the singular plagioclase grain and in the range of a thin section are very comprehensive. Adjoining microfields (10–20 μm distance) exhibit differences in the An-contents between 30 and 80% rel. These observations are valid for nearly 78% of the examined plagioclases. Only in the higher amphibolite facies the An-variations are reduced to an average value of 32% rel. Merely the high temperature plagioclases with a compositional range of An 68-An 79 coexisting with clinopyroxene are largely homogeneous. Their variation is amounting to 6,5% An rel. The epidote chemisms reveal a dependance on both of the different substrata and their oxidation status. The maximum value of the Fe (III) substitution on the M₁ position in the epidote structure is reaching 97 molar per cent at the higher oxidized meta-granitoids and merely 87% at the metabasaltoids. The variations of the Fe/Al-proportions in the microfields are amounting to 5–20% as to the granitoid substrata and to 5–47% rel. as to the basaltoid substrata. In both of the substrata the garnets are very rich of almandine (40–70%). Besides variable amounts of grossularite and pyrope components they also contain 10–20% (basaltoids) and 1–20% (granitoids) spessartine. The most significant element variations are observed for the element Mn in garnets of granitoid origin. These variations attain 46% within the garnet grains. Only for the garnets of the basic substrata from the amphibolite facies one can state a homogenization. The reaction inertia in achieving metamorphic equilibrium is demonstrated by a selected metabasite sample of the amphibolite facies. It seems that only at temperature >600°C a homogenization of the plagioclases and garnets is initiated so that at low temperature a thermometry by means of An-contents in the plagioclases or Mn/Fe-relations in the garnets is not possible.     

Green synthesis of magnetic mesoporous silica nanocomposite and its adsorptive performance against organochlorine pesticides

Green synthesis of nanomaterials has received increasing attention as an eco-friendly technology in materials science. Here, we have used two types of extractions from green tea leaf (i.e., total extraction and tannin extraction) as reducing agents for a rapid, simple and one-step synthesis method of mesoporous silica nanoparticles/iron oxide nanocomposite based on deposition of iron oxide onto mesoporous silica nanoparticles. Mesoporous silica nanoparticles/iron oxide nanocomposite were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray, vibrating sample magnetometer, N₂ adsorption and high-resolution transmission electron microscopy. Mesoporous silica nanoparticles/iron oxide nanocomposite was used as a solid adsorbent for removal of lindane pesticide from aqueous solutions. The developed system possesses the advantages of silica as core that include large surface area and advantages of iron oxide (shell) that include the capability to interact with chlorinated compounds and ability to release by using external magnetic field. UV-Vis technique was used as a simple and easy method for monitoring the removal of lindane. Effects of pH and temperature on the removal efficiency of the developed mesoporous silica nanoparticles/iron oxide nanocomposite toward lindane pesticide were also investigated. Fourier transform infrared spectroscopy, high-performance liquid chromatography and gas chromatography techniques were used to confirm the high ability of mesoporous silica nanoparticles/iron oxide nanocomposite for sensing and the capture of lindane molecules with high sorption capacity (about 99%) that could develop a new eco-friendly strategy for detection and removal of pesticide and as a promising material for water treatment.     

http://www.sciencedirect.com/science/article/pii/S167498711100079X

Lower Paleozoic rocks exposed in various regions of Egypt (south central Sinai, north Eastern Desert and southwest Western Desert), in addition to occurring in the subsurface such as north Western Desert and the Gulf of Suez. The Lower Paleozoic rocks in Egypt include surface and subsurface rock units of formational status. The surface rock units are the Taba, Araba and Naqus formations. The subsurface rock units include the Shifa, Kohla and Basur formations. The Infracambrian Taba Formation has been discovered recently in the outcrops of the south eastern Sinai in the Taba-Ras El-Naqab area. It is missing and/or not recognized in the subsurface. The Taba Formation consists mainly of reddish brown, unfossiliferous gravelly fine-to medium-grained sandstones cemented by kaolinite and have subordinate beds of paleosols. The Cambrian Araba Formation and its subsurface equivalent (the Shifa Formation) are essentially composed of reddish brown, fine-grained laminated sandstone and siltstone with abundant Skolithos and Cruziana sp. In contrast, the Ordovician-Silurian Naqus Formation and its subsurface equivalents (Kohla Formation and Basur Formation) are mainly composed of white, unfossiliferous, cross-bedded, medium- to coarse-grained sandstones with haphazardly distributed pebbles and cobbles. Sedimentological analysis indicates that the Araba Formation and its equivalents were deposited in a marginal-marine environment, whereas the Naqus Formation and its equivalents were laid down in a fluvio-glacial environment. Integrated stratigraphic and sedimentological studies of the Lower Paleozoic rocks permit reconstruction of the paleogeography of Egypt at that time. Egypt has been largely controlled since the Cambrian by the pre-existing structural framework of the pre-Phanerozoic basement rocks inherited from the Late Proterozoic Pan-African event. Additionally, sedimentation processes were controlled during Cambro-Ordovician times by tectonic movements, whereas glacio-eustatic control predominated during the Late Ordovician-Silurian Period. These studies suggest that most areas of Egypt were exposed lands with episodically transgression by epicontinental seas related to the paleo-Tethys. These lands formed a part of a stable subsiding shelf at the northern Gondwana margin.     

Dauphiné twinning and texture memory in polycrystalline quartz. Part 3: texture memory during phase transformation

Samples of quartz-bearing rocks were heated above the α (trigonal)–β (hexagonal) phase transformation of quartz (625–950°C) to explore changes in preferred orientation patterns. Textures were measured both in situ and ex situ with neutron, synchrotron X-ray and electron backscatter diffraction. The trigonal–hexagonal phase transformation does not change the orientation of c- and a-axes, but positive and negative rhombs become equal in the hexagonal β-phase. In naturally deformed quartzites measured by neutron diffraction a perfect texture memory was observed, i.e. crystals returned to the same trigonal orientation they started from, with no evidence of twin boundaries. Samples measured by electron back-scattered diffraction on surfaces show considerable twinning and memory loss after the phase transformation. In experimentally deformed quartz rocks, where twinning was induced mechanically before heating, the orientation memory is lost. A mechanical model can explain the memory loss but so far it does not account for the persistence of the memory in quartzites. Stresses imposed by neighboring grains remain a likely cause of texture memory in this mineral with a very high elastic anisotropy. If stresses are imposed experimentally the internal stresses are released during the phase transformation and the material returns to its original state prior to deformation. Similarly, on surfaces there are no tractions and thus texture memory is partially lost.     

Authigenic carbonate precipitates from the NE Black Sea: a mineralogical,geochemical, and lipid biomarker study

Carbonate precipitates recovered from 2,000 m water depth at the Dolgovskoy Mound (Shatsky Ridge, north eastern Black Sea) were studied using mineralogical, geochemical and lipid biomarker analyses. The carbonates differ in shape from simple pavements to cavernous structures with thick microbial mats attached to their lower side and within cavities. Low δ¹³C values measured on carbonates (−41 to −32‰ V-PDB) and extracted lipid biomarkers indicate that anaerobic oxidation of methane (AOM) played a crucial role in precipitating these carbonates. The internal structure of the carbonates is dominated by finely laminated coccolith ooze and homogeneous clay layers, both cemented by micritic high-magnesium calcite (HMC), and pure, botryoidal, yellowish low-magnesium calcite (LMC) grown in direct contact to microbial mats. δ¹⁸O measurements suggest that the authigenic HMC precipitated in equilibrium with the Black Sea bottom water while the yellowish LMC rims have been growing in slightly ¹⁸O-depleted interstitial water. Although precipitated under significantly different environmental conditions, especially with respect to methane availability, all analysed carbonate samples show lipid patterns that are typical for ANME-1 dominated AOM consortia, in the case of the HMC samples with significant contributions of allochthonous components of marine and terrestrial origin, reflecting the hemipelagic nature of the primary sediment.     

Sr,Nd,Pb Isotope Geochemistry and Magma Evolution of the Potassic Volcanic Rocks,Wudalianchi,Northeast China

Wudalianchi volcanic rocks are the most typical Cenozoic potassic volcanic rocks in easten China.Compositional comparisons between whole rocks and glasses of various occurrences indicate that the magma tends to become rich in silica and alkalis as a result of crystal differentiation in the course of evolu-tion.They are unique in isotopic composition with more radiogenic Sr but less radiogenic Pb.^87Sr/^86Sr is higher and ^143Nd/^144Nd is lower than the undifferentiated global values.In comparison to continental pot-ash volcanic rocks,Pb isotopes are apparently lower.These various threads of evidence indicate that the rocks were derived from a primary enriched mantle which had not been subjected to reworking and shows no sign of incorporation of crustal material.The correlation between Pb and Sr suggests the regional heterogeneity in the upper mantle in terms of chemical composition.