Chromite Mineralization in the Sopcheozero Deposit (Monchegorsk Layered Intrusion, Fennoscandian Shield)

In 1990, the Sopcheozero Cr deposit was discovered in the Monchegorsk Paleoproterozoic layered mafic-ultramafic layered intrusion (Monchepluton). This stratiform early-magmatic deposit occurs in the middle part of the Dunite Block, which is a member of the Monchepluton layered series. The Cr2O3 average-weighted content in ordinary and rich ores of the deposit is 16.65 and 38.76 wt.%, respectively, at gradually changing concentrations within the rich, ordinary and poor ore types and ore body in general. The ores of the Sopcheozero deposit, having a ratio of Cr2O3/FeOtotal = 0.9–1.7, can serve as raw materials for the refractory and chemical industries. The ore Cr-spinel (magnochromite and magnoalumochromite) is associated with highly magnesian olivine (96–98 Fo) rich in Ni (0.4–1.1 wt.%). It confirms a low S content in the melt and complies with the low oxygen fugacity. The coexisting Cr-spinel-olivine pairs crystallized at temperatures from 1258 to 1163 °C, with accessory Cr-spinel crystallizing at relatively low, while ore Cr-spinel at higher temperatures. The host rock and ore distinguish with widespread plastic deformations of olivine at the postcrystallization phase under conditions of high temperature (above 400 °C) and pressure (5 kbar). At the post magmatic Svecofennian stage (1.84 Ga), the deposit, jointly with the Monchepluton, was subject to diverse tectonic deformations.

Petrological and geochemical characterization of the arc-related Suru–Thasgam ophiolitic slice along the Indus Suture Zone, Ladakh Himalaya

The Ladakh Himalayan ophiolites preserve remnants of the eastern part of the Neo-Tethyan Ocean, in the form of Dras, Suru Valley, Shergol, Spongtang and Nidar ophiolitic sequences. In Kohistan region of Pakistan, Muslim Bagh, Zhob and Bela ophiolites are considered to be equivalents of Ladakh ophiolites. In western Ladakh, the Suru–Thasgam ophiolitic slice is highly dismembered and consists of peridotites, pyroxenites and gabbros, emplaced as imbricate blocks thrust over the Mesozoic Dras arc complex along the Indus Suture Zone. The Thasgam peridotites are partially serpentinized with relict olivine, orthopyroxene and minor clinopyroxene, as well as serpentine and iron oxide as secondary mineral assemblage. The pyroxenites are dominated by clinopyroxene followed by orthopyroxene with subordinate olivine and spinel. Gabbros are composed of plagioclase and pyroxene (mostly replaced by amphiboles), describing an ophitic to sub-ophitic textural relationship. Geochemically, the studied rock types show sub-alkaline tholeiitic characteristics. The peridotites display nearly flat chondrite-normalized rare earth element (REE) patterns ((La/Yb)N = 0.6–1.5), while fractionated patterns were observed for pyroxenites and gabbros. Multi-element spidergrams for peridotites, pyroxenites and gabbros display subduction-related geochemical characteristics such as enriched large-ion lithophile element (LILE) and depleted high-field-strength element (HFSE) concentrations. In peridotites and pyroxenites, highly magnesian olivine (Fo88.5-89.3 and Fo87.8-89.9, respectively) and clinopyroxene (Mg no. of 93–98 and 90–97, respectively) indicate supra-subduction zone (SSZ) tectonic affinity. Our study suggests that the peridotites epitomize the refractory nature of their protoliths and were later evolved in a subduction environment. Pyroxenites and gabbros appear to be related to the base of the modern intra-oceanic island-arc tholeiitic sequence.

Mineralogical characterization and evaluation of chromite ore in Grevena and Kozani Vourinos massif, Western Macedonia, Greece

Purpose. Chromite samples from Aetoraches mine area in the southern part of the Vourinos complex in Western Macedonia, Greece were examined from mineralogical-geochemical perspective. Methods. Χ-ray Diffraction (XRD) mineral phase analysis, elemental Scanning Electron Microscopy coupled with Energy Dispersive Spectroscopy (SEM-EDS) analysis and Thermogravimetry/Differential Thermogravimetry (TG/DTG) were carried out. Findings. The XRD results showed that all the samples contain mainly magnesium- and aluminum-chromite (“aluminum-picrochromite”) phases, along with forsterite (magnesian olivine), serpentine and chlorite occurrences. Based on the SEM-EDS results, the computed average chemical formula indicative of this specific chromite type is: (Fe0.4 Mg0.6) (Cr1.6 Al0.4/)O4. The TG-DTG weight losses found to be in the range of 4.4-14.36%, at temperatures between 600 and 750°C, indicated the presence of the hydroxyl-rich silicate minerals, serpentinite and chlorite, in agreement to the Loss of Ignition (LOI) results. The mineral phases detected in the present analyses appear in the dunite/diorite/harzburgite/peridotite main rocks of the ophiolitic complex that hosts the chromite ore. Originality.In the current research, an original characterization, via thorough elemental, phase and thermal analysis, is carried out aiming to enlighten the geochemistry aspects of the Vourinos chromite complex, Region of Western Macedonia, Greece, particularly of easily accessible and exploitable chromite deposits of the Aetoraches mine area. Practical implications. The chromite mineral, and especially the metallurgical type, is of substantial importance in metal industry. In that sense, the findings of the present investigation of chromite purity and mineral structure is a prerequisite for future exploitation of the Aetoraches chromite deposits in particular and broadly for the ongoing exploitation of chromite ore in the Vourinos complex, situated in Region of Western Macedonia, Greece, an area with high unemployment and rather slow economic growth. Keywords: chromite ore, Vourinos massif, Aetoraches mine area, mineralogical characterization, geochemistry, XRD, SEM-EDS, TG/DTG

Mid-crustal storage and crystallization of Eyjafjallajökull ankaramites, South Iceland

Our understanding of the long-term intrusive and eruptive behaviour of volcanic systems is hampered by a relatively short period of direct observation. To probe the conditions of crustal magma storage below South Iceland, we have analysed compositions of minerals, mineral zoning patterns, and melt inclusions from two Eyjafjallajökull ankaramites located at Brattaskjól and Hvammsmúli. These two units are rich in compositionally diverse macrocrysts, including the most magnesian olivine (Fo88-90) and clinopyroxene (Mg#cpx 89.8) known from Eyjafjallajökull. Olivine-hosted spinel inclusions have high Cr#spl (52–80) and TiO2 (1–3 wt%) and low Al2O3 (8–22 wt%) compared to typical Icelandic chromian spinel. The spinel-olivine oxybarometer implies a moderate oxygen fugacity of logFMQ 0–0.5 at the time of crystallization, and clinopyroxene-liquid thermobarometry crystallization at mid-crustal pressures (1.7–4.2 kbar, 3.0±1.4 kbar on average) at 1120–1195°C. Liquid-only thermometry for melt inclusions with Mg#melt 56.1–68.5 and olivine-liquid thermometry for olivine macrocrysts with Fo80.7-88.9 yield crystallization temperatures of 1155–1222°C and 1136–1213°C, respectively. Diffusion modelling of compositional zonations in the Brattaskjól olivine grains imply that the Brattaskjól macrocrysts were mobilized and transported to the surface from their mid-crustal storage within a few weeks (at most in 9–37 days). Trends in clinopyroxene macrocryst compositions and the scarcity of plagioclase indicate that the mid-crustal cotectic assemblage was olivine and clinopyroxene, with plagioclase joining the fractionating mineral assemblage later. In all, the crystal cargoes in the Brattaskjól and Hvammsmúli ankaramites are composed of agitated wehrlitic or plagioclase wehrlitic crystal mushes that crystallized over a large temperature interval at mid-crustal depths.

Low-T formation of high-Cr spinel with apparently primary chemical characteristics within podiform chromitite from Rayat, northeastern Iraq

Chemical modification of chromian spinel at low-T alteration was examined in detail for a podiform chromitite from a Tethyan ophiolitic mélange belt at Rayat, northeastern Iraq. The chromitite is highly brecciated and the matrix has been completely altered, producing chlorite and carbonate (dolomite and calcite). High-Cr, low-Fe3+ spinel has formed along the margins and cracks of chromian spinel grains throughout the alteration, associated with unaltered primary spinel and magnetite without ferritchromite. In associated harzburgites, only ferritchromite is found instead of the high-Cr, low-Fe3+ spinel. The high-Cr, low-Fe3+ secondary spinel apparently has chemical properties of mantle origin, plotted at the extension of ordinary mantle spinels on compositional spaces. The character is due to subtraction of Al as chlorite with the addition of an amount of magnetite component from the silicate matrix, which is small in volume relative to peridotite and composed of highly magnesian olivine (up to Fo97). We should treat high-Cr chromian spinels with caution in highly altered mantle-derived rocks, especially chromitite and other rocks with highly magnesian olivine, as well as in detrital particles for provenance study.