Effect of heat treatment on tourmaline from Brazil

The crystal-chemical behaviour of tourmaline from Araçuaí, Minas Gerais state, Brazil, when subjected to heating in air atmosphere has been studied by several techniques, including EMPA, UV–Vis, TGA, and Mössbauer spectroscopy. The tourmaline samples are typically intermediate members of the elbaite-schorl series. The origin of colour and of its change after treatment has been discussed in terms of local disorder, presence of metal transition elements, oxidation of ferrous iron at the octahedral site, and simultaneous trap of the excess electron. These findings may be used to enhance the colour in tourmaline crystals or generate wanted colour changes.     

Eclogite and carpholite-bearing metasedimentary rocks in the North Qilian suture zone, NW China: implications for Early Palaeozoic cold oceanic subduction and water transport into mantle

Low‐temperature eclogite and eclogite facies metapelite together with serpentinite and marble occur as blocks within foliated blueschist that was originated from greywacke matrix; they formed a high‐pressure low‐temperature (HPLT) subduction complex (mélange) in the North Qilian oceanic‐type suture zone, NW China. Phengite–eclogite (type I) and epidote–eclogite (type II) were recognized on the basis of mineral assemblage. Relic lawsonite and lawsonite pseudomorphs occur as inclusions in garnet from both types of eclogite. Garnet–omphacite–phengite geothermobarometry yields metamorphic conditions of 460–510 °C and 2.20–2.60 GPa for weakly deformed eclogite, and 475–500 °C and 1.75–1.95 GPa for strongly foliated eclogite. Eclogite facies metasediments include garnet–omphacite–phengite–glaucophane schist and various chloritoid‐bearing schists. Mg‐carpholite was identified in some high‐Mg chloritoid schists. P–T estimates yield 2.60–2.15 GPa and 495–540 °C for Grt–Omp–Phn–Gln schist, and 2.45–2.50 GPa and 525–530 °C for the Mg‐carpholite schist. Mineral assemblages and P–T estimates, together with isotopic ages, suggest that the oceanic lithosphere as well as pelagic to semi‐pelagic sediments have been subducted to the mantle depths (≥75 km) before 460 Ma. Blueschist facies retrogression occurred at c. 454–446 Ma and led to eclogite deformation and dehydration of lawsonite during exhumation. The peak P–Tconditions for eclogite and metapelite in the North Qilian suture zone demonstrate the existence of cold subduction‐zone gradients (6–7 °C km^?1), and this cold subduction brought a large amount of H₂O to the deep mantle in the Early Palaeozoic times.     

Aqueous uptake of uranium onto pyrite surfaces; reactivity of fresh versus weathered material

In order to better understand the interaction between aqueous uranium and pyrite (FeS₂) the uptake of uranium onto the surfaces of both weathered and freshly generated pyrite surfaces was examined using batch sorption experiments. Analysis was performed using X-ray photoelectron spectroscopy (XPS). The results clearly indicate that freshly polished pyrite surfaces are efficient scavengers of uranium from solution, while weathered surfaces exhibit only limited uptake. Results also indicate partial reduction of uranium at the pyrite surfaces, with a heterogeneous distribution of U(IV) and U(VI) species.     

Timing and setting of skarn and iron oxide formation at the Smältarmossen calcic iron skarn deposit, Bergslagen, Sweden

Abundant iron oxide deposits including banded iron formations, apatite iron oxide ores, and enigmatic marble/skarn-hosted magnetite deposits occur in the Palaeoproterozoic Bergslagen region, southern Sweden. During the last 100 years, the latter deposit class has been interpreted as contact metasomatic skarn deposits, metamorphosed iron formations, or metamorphosed carbonate replacement deposits. Their origin is still incompletely understood. At the Smältarmossen mine, magnetite was mined from a ca. 50-m-thick calcic skarn zone at the contact between rhyolite and stratigraphically overlying limestone. A syn-volcanic dacite porphyry which intruded the footwall has numerous apophyses that extend into the mineralized zone. Whole-rock lithogeochemical and mineral chemical analyses combined with textural analysis suggests that the skarns formed by veining and replacement of the dacite porphyry and rhyolite. These rocks were added substantial Ca and Fe, minor Mg, Mn, and LREE, as well as trace Co, Sn, U, As, and Sr. In contrast, massive magnetite formed by pervasive replacement of limestone. Tectonic fabrics in magnetite and skarn are consistent with ore formation before or early during Svecokarelian ductile deformation. Whereas a syngenetic–exhalative model has previously been suggested, our results are more compatible with magnetite formation at ca. 1.89 Ga in a contact metasomatic skarn setting associated with the dacite porphyry.     

The Taihua group on the southern margin of the North China craton: further insights from U–Pb ages and Hf isotope compositions of zircons

The "Taihua Group" is a collective term for a series of old terranes scattered along the southern margin of the North China Craton. The timing of formation and thermal overprinting of the Taihua Group have long been contentious, and its relationship with the Qinling orogenic belt has been unclear. In this study, new data from integrated in-situ U–Pb dating and Hf isotope analysis of zircons from an amphibolite (from the Xiong’ershan terrane) and a biotite gneiss (from the Lantian-Xiaoqinling terrane) indicate that the Upper Taihua Group formed during the Paleoproterozoic (2.3–2.5 Ga) and thus was originally part of the southern edge of North China Craton, detached during the Mesozoic Qinling orogeny and displaced about 100 km north from its original location. This suggests that the Taihua Group became part of the tectonic terrane associated with the Qinling orogeny and now forms part of the overthrust basement section of the Qinling belt. Before the Qinling orogeny, the Taihua Group was metamorphosed at 2.1 Ga. The initial Hf-isotope compositions of zircons, together with positive εNd(t) values for the whole-rocks, imply that the original magmas were derived from a juvenile source with some assimilation of an Archean crustal component.     

Diamond crystallization in the Fe-Co-S-C and Fe-Ni-S-C systems and the role of sulfide-metal melts in the genesis of diamond

Diamond crystals 0.1–0.8 carats were synthesized in experiments conducted in a BARS split-sphere multianvil high-pressure apparatus in the systems Fe-Co-S-C and Fe-Ni-S-C at a pressure of 5.5 GPa and temperature of 1300°C. The microtextures of the samples and the phases accompanying diamond (carbides, graphite, monoslufide solid solution, pentlandite, and taenite) are examined in much detail, the properties of metal-sulfide-carbon alloys are discussed, and issues related to the genesis of sulfide inclusions in diamonds and graphite crystallization in the diamond stability field are considered. The experiments demonstrate that diamonds can be synthesized and grow in pre-eutectic metal-sulfide melts with up to 14 wt % sulfur at relatively low P-T parameters, which correspond to the probable temperatures and pressures of natural diamond-forming processes at depths of approximately 150 km in the Earth’s upper mantle.     

New data on distribution of REEs in sulfide minerals and Sm-Nd dating of ore genesis of layered basic intrusions

This paper presents data on the distribution of REEs in sulfide minerals from ore-bearing gabbronorites in the Penikat layered intrusion and the results of their isotopic-geochronological Sm-Nd study. A new procedure for determination of REEs in the samples without preliminary separating and concentrating was tested on standard samples to be further used for analysis of sulfide minerals. Analysis of the spectra of the REE distribution in sulfides represents a distribution trend that is similar to the already studied bulk rock and allows deducing that the character of the REE distribution in sulfide minerals from gabbronorites in the Penikat layered intrusion was inherited from the parent magma melt; while the formation of sulfides took place at the stage of rock crystallization. The performed complex studies allow considering that sulfides can be successfully used together with the rock-forming minerals in Sm-Nd dating of ore-bearing mafite-ultramafite intrusions.     

Fluxes of organic carbon in Manukau Harbour, New Zealand

We collated information on the sources and sinks of organic carbon in Manukau Harbour, a shallow temperate estuary. Two contrasting inner harbor regions were considered; the northern region, which is urbanized and receives a major load of sewage wastewater, and the southern region, where allochthonous inputs are dominated by the runoff from small rural streams. Although high levels of dissolved nitrogen in the wastewater supported phytoplankton blooms in the northern region, total primary production there was similar to that in the southern region (ca. 300 g C m^?2yr^?1). By contrast, high concentrations of organic carbon in the wastewater resulted in an additional input to the northern region of 120 g C m^?2 yr^?1. Loads from runoff and streams to both regions were low. At 350 g C m^?2 yr^?1, total respiration in the northern region exceeded total production, so the region was slightly heterotrophic. Respiration was lower in the southern region (270 g C m^?2 yr^?1), which was net autotrophic. Some carbon was exported from each region to the outer harbour (50–80 g C m^?2 yr^?1). Dissolved oxygen levels in the northern region were somewhat depleted at times; and the high numbers of microzooplankton indicated consumption was enhanced there. Apart from a relatively small area of organic enrichment close to the wastewater discharge, benthic consumers in the harbor appeared to be limited by physical disturbance (by wind-waves) rather than by food availability. Improved wastewater treatment is expected to substantially reduce the allochthonous input to the northern region, with the total input of carbon in the future being only slightly higher than that to the southern region.     

Infrared reflectivity spectra of single crystal cassiterites

The infrared reflectivity spectra of two natural cassiterite single crystals from Portugal and Vietnam have been studied and analysed in the frequency range of 15–4000 cm^–1 at room temperature. The optical mode parameters are deduced by simulation of the experimental spectra using the factorised form of the dielectric function. The difference with synthetic SnO₂ spectra is a dip near 500 cm^–1 understood as the activation of an infrared forbidden E _g mode due to the amount of Fe³⁺ and Ti⁴⁺ impurities. Another result of this work is the derivation of the correct values of the static dielectric constant of cassiterite.     

Fluorine and chlorine in apatites,micas, and amphiboles of layered trap intrusions of the Siberian Platform

Geochemistry of chlorine and fluorine in apatites, micas, and amphiboles in rocks from eight intrusive complexes of the Siberian Platform has been first studied on the basis of new factual and analytical data (more than 1000 analyses). The main attention is focused on minerals from layered intrusions. Most apatites show F > Cl; the maximum contents of halogens are specific to chlorapatite (6.97 wt.% Cl) and fluorapatite (6.04 wt.% F). The total f value (f = Fe/(Fe + Mg), at.%) of femic minerals varies from 2 to 98 at.% in micas and from 22 to 95 at.% in amphiboles. The Cl-f and F-f trends show an increase in the Cl content and a decrease in the F content in the minerals with increasing f. Chlorine clearly exhibits ferrophilic properties, and fluorine has magnesiophilic properties. The halogen-richest minerals are fluorophlogopite (F = 7.06 wt.%, f = 7 at.%), chlorannite (Cl = 6.30 wt.%, f = 89 at.%), and chloroferrihastingsite (Cl = 5.22 wt.%, f = 90 at.%). Coexisting micas and amphiboles in the rocks are close in f value, but the micas are richer in Cl than the amphiboles. We assume that the halogen-containing minerals crystallized at the high pressure of halogen-hydrocarbon fluids at the levels of the MW, IW, and QIF buffers. The reducing conditions of the magmatism process are also evidenced by the presence of graphite and native metals in the rocks. The similarity of the Cl-f and F-f trends of micas and amphiboles from different intrusive complexes indicates the same mechanisms of the melt differentiation and mineral crystallization.