Rare-earth abundances in kimberlites from Greenland and Zambia

Ten rare-earth elements (La, Ce, Nd, Sm, Eu, Gd, Tb, Tm, Yb and Lu) and Ta, Th and Hf contents in eight kimberlites and inclusions from Greenland and Zambia have been determined by instrumental neutron activation. All the samples have highly fractionated rare-earth (REE) distribution patterns. La/Yb ratios in the Greenland kimberlites (hypabyssal facies) vary from 111.8 to 188.4, and the total rare-earth contents range from 204.8 to 380.3 ppm. No europium anomaly is present. The Zambian kimberlites (diatreme facies) are altered and carbonated. Rare-earth patterns in these are also light REE-enriched. A significant difference is shown to exist between the diatreme and hypabyssal facies of kimberlites.     

Late-Stage Mafic Injection and Thermal Rejuvenation of the Vinalhaven Granite, Coastal Maine

The Vinalhaven intrusive complex consists mainly of coarse-grainedgranite, inward-dipping gabbro–diorite sheets, and a fine-grainedgranite core. Small bodies of porphyry occur throughout thecoarse-grained granite. The largest porphyry body (roughly 0·5km by 2·5 km) occurs with coeval gabbro, hybrid rocks,and minor fine-grained granite in the Vinal Cove complex, whichformed during the waning stages of solidification of the coarse-grainedVinalhaven granite. Porphyry contacts with surrounding coarse-grainedgranite are irregular and gradational. Compositions of wholerocks and minerals in the porphyry and the coarse-grained graniteare nearly identical. Neighboring phenocrysts in the porphyryvary greatly in degree of corrosion and reaction, indicatingthat the porphyry was well stirred. Thermal rejuvenation ofa silicic crystal mush by a basaltic influx can explain thecomposition and texture of the porphyry. Comparable rejuvenationevents have been recognized in recent studies of erupted rocks.Weakly corroded biotite phenocrysts in the porphyry requirethat hydrous interstitial melt existed in the granite duringremelting. Field relations, along with thermal calculations,suggest that cooling and crystallization of coeval mafic magmacould have generated the porphyry by thermal rejuvenation ofgranite crystal-mush containing about 20% melt. Field relationsalso suggest that some of the porphyry matrix may representnew felsic magma that was emplaced during remelting. KEY WORDS: granite; magma chamber; mafic replenishment; rejuvenation     

The Kovdor apatite-francolite deposit as a prospective source of phosphate ore

The mineral and chemical composition of phosphate ore, its texture and structure, and the distribution of trace elements are considered based on the results of geological exploration of the Kovdor apatitefrancolite deposit carried out in 2010–2012. The compositions of major, minor, and accessory minerals are reported. The ore varieties are typified depending on their composition, quality, texture, structure, and concentrating ability. The apatite-francolite ore occupies a certain position in the lateritic profile of carbonatite weathering and is of residual-infiltration origin as a zone of secondary phosphate enrichment. The outlook of the Kovdor deposit for this type of ore as a whole is considered in the context of phosphorus ore potential enhancement.     

The Timescales of Magma Mixing in the Plumbing System of Bezymianny Volcano (Kamchatka): Insights from Diffusion Chronometry

Intrusion of magma of contrasting composition into a magma chamber often triggers eruptions of arc volcanoes. Application of the diffusion chronometry method allowed us to determine the time when fresh magma was supplied to the shallow chamber of Bezymianny volcano in the case of six eruptions in 2006–2012 and to compare them to the recorded seismic activity of this volcano. Two types of eruptions of Bezymianny volcano were distinguished, with a contrasting orthopyroxene rim being formed in the respective magmas (a) up to 3 years and (b) up to 2 months before the beginning of an eruption. It was shown that these differences are caused by two different paths of magma supply to the shallow chamber of Bezymianny volcano.     

The Cerro Morado Andesites: Volcanic history and eruptive styles of a mafic volcanic field from northern Puna, Argentina

The Upper Miocene Cerro Morado Andesites constitutes a mafic volcanic field (100 km²) composed of andesite to basaltic andesite rocks that crop out 75 km to the east from the current arc, in the northern Puna of Argentina. The volcanic field comprises lavas and scoria cones resulting from three different eruptive phases developed without long interruptions between each other. Lavas and pyroclastic rocks are thought to be sourced from the same vents, located where orogen-parallel north-south faults crosscut transverse structures.The first eruptive phase involved the effusion of extensive andesitic flows, and minor Hawaiian-style fountaining which formed subordinate clastogenic lavas. The second phase represents the eruption of slightly less evolved andesite lavas and pyroclastic deposits, only distributed to the north and central sectors of the volcanic field. The third phase represents the discharge of basaltic andesite magmas which occurred as both pyroclastic eruptions and lava effusion from scattered vents distributed throughout the entire volcanic field. The interpreted facies model for scoria cones fits well with products of typical Strombolian-type activity, with minor fountaining episodes to the final stages of eruptions.Petrographic and chemical features suggest that the andesitic units (SiO₂ > 57%) evolved by crystal fractionation. In contrast, characteristics of basaltic andesite rocks are inconsistent with residence in upper-crustal chambers, suggesting that batches of magmas with different origins or evolutive histories arrived at the surface and erupted coevally.Based on the eruptive styles and lack of volcanic quiescence gaps between eruptions, the Cerro Morado Andesites can be classified as a mafic volcanic field constructed from the concurrent activity of several small, probably short-lived, monogenetic centers.     

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.     

Mesozoic age of granitoids from the Beket complex (Gonzha block within the Argun terrane of the Central-Asian Fold Belt)

U-Pb geochronological results confirm the Mesozoic age (124 ± 1 Ma) of the Beket granitoid complex, previously interpreted as being one of the markers amongst the Early Proterozoic magmatic complexes within the Amur superterrane (microcontinent) of the Central Asian Fold Belt. This implies that the structural and metamorphic amphibolite facies overprints documented either in the Beket granitoids or Gonzha host rocks are evidently Mesozoic rather than Early Proterozoic in age.     

Low molecular weight polyacrylamide-based polymers as modifiers in phosphate beneficiation

The phosphate industry currently uses several natural polymers such as starch and guar as modifiers to achieve better separation of phosphate from silicates and carbonates. These natural products have many drawbacks: poor selectivity, low performance/dosage ratio, instability and sensitivity to aging, batch variability in composition, and deleterious down-stream effects. Several new, synthetic, low molecular weight polymers have recently been developed as cost-effective alternatives to natural products. These polymers have not only overcome many of the problems associated with natural products, but also have high activity and selectivity.The approach used in designing the synthetic polymers was to incorporate functional groups that would adsorb selectively on the mineral surface thereby rendering it hydrophilic. The phosphate modifier (depressant) developed recently is a low molecular weight polyacrylamide containing both hydroxyl and carboxylic acid functional groups. This polymer has provided excellent selectivity in the separation of apatite from siliceous gangue. The role of this and related polymers in the selective cationic flotation of quartz from apatite is discussed in this paper. The structure-activity relationships have been studied by determining the modifier activity of a range of polyacrylamides containing hydroxyl, carboxyl or carboxymethylol groups.     

Mineral chemistry of clays associated with the Jhilmili intertrappean bed in the eastern Deccan volcanic province: Palaeoenvironmental inferences and KTB transition

Jhilmili intertrappean bed (～13 m thick) attains its significance with the recent discovery of brackish water ostrocod and planktonic foraminifera fossils (Keller et al. 2009; Khosala et al. 2009). Present XRD data revealed abundance of montmorillonite > montmorillonite/chlorite mixed layer > palygorskite in five physically distinct lithounits namely: (a) lower chocolate brown siltstone with green patches, followed by (b) brick red clayey siltstone, (c) greenish grey clay, (d) yellowish brown clay and (e) uppermost olive grey to dark brown silt layers in the successionrepresent higher weathering indices and annual precipitation, reflecting cyclic, but longer spells of weathering. Occurrence of M/C mixed layer with the smectite in Jhilmili area is suggestive of their derivation from the later, whilst montmorillonite to palygorskite transformation is ascribed to the drastic changes in the humid to arid climate, where former served as a source of Al and some of the Si and Mg ions for the later. Jhilmili and Anjar clays represent similar charge occupancies at different sites, but later contains relatively higher amount of palygorskite, formed in the arid environment. Majority of the trace elemental data plots for Jhilmili clays lie within the upper and lower limits of infra (Lametas)-/inter-trappeans clays. The continuous release of Cu throughout the succession (mainly in the palygorskite dominated clays) indicates oxidizing conditions. PAAS normalized REE data plots for these clays show progressive enrichment in the HREE contents in the lower part, but, upper part of the succession is marked by positive cerium anomaly, reflecting oxidizing conditions prevailed at the later stage of the succession. These conditions continued, but, were not conducive to HREE enrichment as evidenced by their depletion in the upper part of the succession. The Ce anomaly observed in the middle part of the succession is similar to that form by continental weathering of the basalt, ascribed to Ce precipitation in the oxic environment, thus suggestive of drastic changes in the oxidizing conditions. Thermodynamic data-sets for Jhilmili clays show I/S mixed layer and celadonite compositions, whereas, Jabalpur infra-/inter-trappean clays correspond to Mg smectites and celadonite end members, thus, representing compositional commonality with those of the other clays derived from the continental weathering of basalt protolith. Jhilmili smectites and smectite-chlorite mixtures show compositional similarity with the dioctahedral and trioctahedral smectites and the smectites formed at 250°C, having compositions between trioctahedral smectite and chlorite, thus, assigning high temperatures for their formation, where the heat required for the formation of these clays was possibly derived from the hydrothermal fluids, associated with the Deccan volcanism.     

Extraction procedure testing of solid wastes generated at selected metal ore mines and mills

Solid waste samples from a reconnaissance study conducted at ore mining and milling sites were subjected to the U.S. Environmental Protection Agency extraction procedure (EP) leaching test Sites visited included mines and mills extracting ores of antimony (Sb), mercury (Hg), vanadium (V), tungsten (W), and nickel (Ni). Samples analyzed included mine wastes, treatment pond solids, tailings, low grade ore, and other solid wastes generated at these facilities Analysis of the leachate from these tests indicates that none of the samples generated leachate in which the concentration of any toxic metal parameter exceeded EPA criteria levels for those metals. By volume, tailings generally constitute the largest amount of solid wastes generated, but these data indicate that with proper management and monitoring, current EPA criteria can be met for tailings and for most solid wastes associated with mining and milling of these metal ores. Long-term studies are needed to determine if leachate characteristics change with time and to assist in development of closure plans and post closure monitoring programs.