Fluid inclusion studies of the Abawso gold prospect,near the Ashanti Belt,Ghana

The major Ghanaian lode gold deposits are preferentially aligned along the western and eastern contacts of the Kumasi Basin with the Ashanti and Sefwi Belts, respectively. The investigated area of the Abawso small-scale concession, covering the workings of the old Ettadom mine, is situated 3 km west of the lithological contact of the Birimian metavolcanic rocks of the Akropong Belt in the east with the Birimian metasedimentary rocks of the Kumasi Basin in the west. The rocks of the Abawso concession represent a steeply NW-dipping limb of a SE-verging anticline with an axis plunging to the SW. Quartz veining occurs predominantly in the form of en échelon dilatational veins along NNE–SSW-striking shear zones of a few metres width and shows evidence of brittle and ductile deformation. Also stockwork-style quartz veining occurs in the vicinity of the main shaft of the old Ettadom mine. Hydrothermal alteration includes sericitisation, sulphidation and locally carbonatisation. The auriferous quartz veins mainly follow the trend of brittle to ductile deformed quartz veins; however, some occur in stockwork. Fluid inclusion studies reveal a large number of H₂O inclusions along intragranular trails in auriferous quartz vein samples, as well as an overall dominance of H₂O and H₂O-CO₂ inclusions over CO₂ inclusions. Textural observations and physico-chemical fluid inclusion properties indicate post-entrapment modifications for all quartz vein samples due to grain boundary migration recrystallisation. This process is interpreted to be responsible for the generation of the CO₂ inclusions from a H₂O-CO₂ parent fluid. In comparison with mineralisation at the Ashanti and Prestea deposits, which are characterised by CO₂±N₂ inclusions, the observed inclusion assemblage may be due to a shallower crustal level of mineralisation, or different degrees and styles of recrystallisation, or a less pronounced development of laminated quartz veins due to comparably restricted pressure fluctuations. Furthermore, the microthermometric observations allow the reconstruction of a possible retrograde P-T path, depicting near-isothermal decompression in the P-T range of the brittle/ductile transition.Editorial handling: E. Frimmel     

Factors controlling the adsorption of acid blue 113 dye from aqueous solution by dried <Emphasis Type="Italic">C. edulis</Emphasis> plant as natural adsorbent

Contamination of surface water and groundwater by organic pollutants is a serious problem due to their persistence, bioaccumulation and biomagnification through food webs. Since the removal of dyes from wastewater is considered an environmental challenge and government legislation requires textile wastewater to be treated, therefore there is a constant need to have an effective process that can efficiently remove these dyes. The aim of the present study is to evaluate the potentiality of dried Carpobrotus edulis plant as low-cost adsorbent for the removal of the industrial acid blue 113 dye from aqueous solutions using the batch equilibration technique. The effects of different physicochemical parameters such as adsorbent dose, contact time, initial dye concentration, solution pH and temperature on adsorption rate of anionic AB113 dye on microparticles of dried C. edulis plant were investigated. The experimental data were analyzed by using mathematical models to determine the thermodynamic parameters. The negative values of free energy change indicated the spontaneous nature of the adsorption and negative value of enthalpy change suggested the exothermic nature of the adsorption process. These results indicate that dried C. edulis plant as an environmentally friendly adsorbent could be potentially used for the removal of anionic dyes from aqueous solutions.     

矿物学文献中未定名矿物的编码系统:国际矿物学协会新矿物与命名和分类委员会“未定名矿物”小组报告

国际矿物学协会新矿物与命名和分类委员会(IMA-CNMMN)的未定名矿物小组(SUM),开发了一个编码系统,对已经发表但尚未定名的矿物进行编码。在文献中存在两类未定名矿物。一是"有效"未定名矿物,是指未定名矿物没有对应的已知矿物种,但如果它们有其他产地或能够在其他样品中被发现,那么已发表的相关矿物描述允许得到认可。二是"无效"未定名矿物,是指未定名矿物已经有对应的已知矿物种;或者相关矿物描述不足以获得认可。未定名矿物的名单是由IMA保管。该编码系统提供了一个永久的UM号码。中国的矿物学文献的数量和重要性有必要用中文阐述未定名矿物的编码系统。     

The Late Silurian Age of the Reference Aralaul Granosyenites–Granite Massif (Northern Kazakhstan)

This work presents the results of U–Pb geochronological studies of alkaline granites of the Aralaul complex of Northern Kazakhstan, which allow one to substantiate their Late Silurian (420 ± 4 Ma) age. Taking into consideration the previously obtained data, we propose a new development scheme of Paleozoic granitoid magmatism in Northern Kazakhstan, which includes Late Ordovician granite–granodiorite (Zerenda and Krykkuduk), Early Silurian granite–leucogranite (Borovoe and Karabulak), Late Silurian granosyenites–granite (Aralaul), and Early Devonian (Balkashino and Orlinogorsk) complexes.     

Chloritöid-pyrophyllite-rectorite facies rocks from Brittany,France

Electron microprobe analyses of minerals in low grade metamorphic sandy black shales of middle Paleozoic age indicate that chemical equilibrium was closely approached in authigenic ferro-magnesian or alkali-bearing phases while aluminum silicate minerals appear to have reacted at a slower rate. The K for Mg-Fe in chlorite-chloritöid pairs is 0.19, the latter phase being iron-rich. The pseudomorphism of detrital white micas produces kaolinite, pyrophyllite and intimate mixtures of muscoviteparagonite. New phases forming in other sites include chlorite, chloritöid and rectorite which is an ordered paragonitebeidellite mixed layered phase. These minerals were formed at temperatures below 280° C. This is just above the stability of the illite-smectite mixed layered minerals which have an ISII ordering sequence (85 to 95% illite). It was noted that ferromagnesian minerals attain chemical equilibrium on a thin-section scale while the aluminous phases often seem to respond to chemical potentials operative on a submillimetric scale.     

Friedrichbeckeite, K (□0.5Na0.5)2 (Mg0.8Mn0.1Fe0.1)2 (Be0.6 Mg0.4)3 [Si12O30], a new milarite-type mineral from the Bellerberg volcano, Eifel area, Germany

Friedrichbeckeite is a new milarite-type mineral. It was found in a single silicate-rich xenolith from a quarry at the Bellerberg volcano near Ettringen, eastern Eifel volcanic area, Germany. It forms thin tabular crystals flattened on {0001}, with a maximum diameter of 0.6 mm and a maximum thickness of 0.1 mm. It is associated with quartz, tridymite, augite, sanidine, magnesiohornblende, enstatite, pyrope, fluorapatite, hematite, braunite and roedderite. Friedrichbeckeite is light yellow, with white to light cream streak and vitreous lustre. It is brittle with irregular fracture and no cleavage, Mohs hardness of 6, calculated density is 2.686 gcm^?3. Optically, it is uniaxial positive with n_ω = 1.552(2) and n_ε = 1.561(2) at 589.3 nm and a distinct pleochroism from yellow (//ω) to light blue (//ε). Electron microprobe analyses yielded (wt.%): Na₂O 2.73, K₂O 4.16, BeO 4.67, MgO 11.24, MnO 2.05, FeO 1.76, Al₂O₃ 0.15, SiO₂ 73.51, (Σ CaO, TiO₂ = 0.06) sum 100.33 (BeO determined by LA-ICP-MS). The empirical formula based on Si = 12 is K_0.87 Na_0.86 (Mg_1.57Mn_0.28Fe_0.24)_Σ2.09 (Be_1.83?Mg_1.17)_Σ3.00 [Si₁₂O₃₀], and the simplified formula can be given as K (□_0.5Na_0.5)₂ (Mg_0.8Mn_0.1Fe_0.1)₂ (Be_0.6?Mg_0.4)₃ [Si₁₂O₃₀]. Friedrichbeckeite is hexagonal, space-group P6/mcc, with a = 9.970(1), c = 14.130(3) Å, V = 1216.4(3) ų, and Z = 2. The strongest lines in the X-ray powder diffraction pattern are (d in Å / I _obs / hkl): 3.180 / 100 / 121, 2.885 / 70 / 114, 4.993 / 30 / 110, 4.081 / 30 / 112, 3.690 / 30 / 022. A single-crystal structure refinement (R1 = 3.62 %) confirmed that the structure is isotypic with milarite and related ^[12] C ^[9] B ₂ ^[6] A ₂ ^[4] T2₃ [^[4] T1₁₂O₃₀] compounds. The C-site is dominated by potassium, the B-site is almost half occupied by sodium, and the A-site is dominated by Mg. The site-scattering at the T2-site can be refined to a Be/(Be?+?Mg) value close to 0.61; the T1-site is occupied by Si. Micro-Raman spectroscopy reveals an increasing splitting of scattering bands around 550 cm^?1 for friedrichbeckeite. The mineral can be classified as an unbranched ring silicate or as a beryllo-magnesiosilicate. With respect to the end-member formula K (□0.5Na0.5)₂ Mg₂ Be₃ [Si₁₂O₃₀] friedrichbeckeite represents the Mg-dominant analogue of almarudite, milarite or oftedalite. The mineral and its paragenesis were formed during pyrometamorphic modifications of the silicate-rich xenoliths enclosed in Quaternary leucite-tephritic lava of the Bellerberg volcano. Holotype material of friedrichbeckeite has been deposited at the mineral collection of the Naturhistorisches Museum Wien, Austria. The mineral is named friedrichbeckeite in honour of the Austrian mineralogist and petrographer Friedrich Johann Karl Becke (1855–1931).     

Sodian stellerite from Capo Pula,Sardegna

The sodian stellerite (a zeolite) occurs as lustrous white or slightly pink, easily cleavable lamellae, filling cavities and fractures in an acid lava (andesite or rhyolite) in the cliff below S. Efisio Tower, near Capo Pula, Cagliari, Sardegna, Italy. The principal forms present are {010}, {011}, {111}. Single crystal photographs show an orthorhombic symmetry and Ammm (or Ammm) space group. An indexed X-ray diffraction powder pattern is provided. Unit cell dimensions, chemical formula, density, optical properties and thermal behaviour are given.     

Dunites of the Inagli massif (Central Aldan), cumulates of lamproitic magma

We consider a hypothesis for the origin of PGE-bearing ultramafic rocks of the Inagli massif (Central Aldan) through fractional crystallization from ultrabasic high-potassium magma. We studied dunites and wehrlites of the Inagli massif and olivine lamproites of the Ryabinovy massif, which is also included into the Central Aldan high-potassium magmatic area. The research is focused on the chemistry of Cr-spinels and the phase composition of Cr-spinel-hosted crystallized melt inclusions and their daughter phases. Mainly two methods were used: SEM-EDS (Tescan Mira-3), to establish different phases and their relationships, and EPMA, to obtain precise chemical data on small (2-100 μm) phases. The obtained results show similarity in chromite composition and its evolutionary trends for the Inagli massif ultramafites and Ryabinovy massif lamproites. The same has been established for phlogopite and diopside from crystallized melt inclusions from the rocks of both objects. Based on the results of the study, the conclusion is drawn that the ultramafic core of the Inagli massif resulted from fractional crystallization of high-potassium melt with corresponding in composition to low-titanium lamproite. This conclusion is consistent with the previous hypotheses suggesting an ultrabasic high-potassium composition of primary melt for the Inagli ultramafites.     

Temporal and tectonic evolution of the granulite-eclogite association from the Bergen Arcs, western Norway

The U-Pb and Sm-Nd dating of deep crustal rocks from the Bergen Arcs system helps resolve enigmatic aspects of the tectonic evolution of the Caledonian Orogen in western Norway and yields insights into the arrested stages of eclogite development within the granulites of the area. The U-Pb dating of zircon from one of the eclogite facies shear zones yields an upper intercept age of 945 ± 5 Ma [all errors two standard deviations (2σ)], which is similar to other zircon ages from the granulite facies protolith. The age is interpreted to represent the time of late Proterozoic (Sveconorwegian) granulite metamorphism. The U-Pb ages of sphene and epidote show that the eclogites formed early in the evolution of the Caledonian Orogen (pre-Scandian phase) at about 460 Ma. An eclogite facies quartz vein yields a Sm-Nd whole rock-garnet isochron of 440 ± 12 Ma that may reflect the onset of cooling immediately after peak eclogite facies conditions, although the Sm-Nd systematics reveal some isotopic disequilibrium within the sample. In tandem with previous ⁴⁰Ar/³⁹Ar age determinations from, an adjacent eclogite of 450 Ma for hornblende and 430 Ma for muscovite, these data indicate that < 30 Ma elapsed between formation of the eclogites and the initial stages of cooling and exhumation to at least mid-crustal levels. This corresponds to minimum cooling rates of 14 °C/m.y. The timing relations suggest that the formation and exhumation of these eclogites from the overlying Caledonian Nappe wedge in western Norway are related to an early phase of crustal subduction during or somewhat before the major phase of continent-continent collision.

The short period of time between the formation of the eclogites and the initial stages of exhumation and rapid cooling is consistent with the only partial and localized transformation of the granulite to eclogite. Isolated occurrences of eclogite within the granulite, the formation of eclogite along metasomatic fronts and the formation of hydrous eclogite facies minerals within the “dry” granulite all point to the importance of fluids in the transformation and re-equilibration of the granulite to eclogite. Together, field and isotopic data demonstrate that both the localized and limited access of fluids and the rapid cycling of continental crust through the deepest portions of the orogen to upper crustal levels resulted in the preservation of the arrested stages of eclogite formation and survival of the granulites metastably through eclogite facies conditions.