Nb–Ta–(Ti–Sn) oxide mineral chemistry as tracer of rare-element granitic pegmatite fractionation in the Borborema Province,Northeastern Brazil

The Borborema Pegmatitic Province (BPP), northeastern Brazil, is historically important for tantalum mining and also famous for top-quality specimens of exotic Nb–Ta oxides and, more recently, for the production of gem quality, turquoise blue, ‘Paraíba Elbaite.’ With more than 750 registered mineralized rare-element granitic pegmatites, the BPP extends over an area of about 75 by 150 km in the eastern part of the Neoproterozoic Seridó Belt. The Late Cambrian pegmatites are mostly hosted by a sequence of Neoproterozoic cordierite–sillimanite biotite schists of the Seridó Formation and quartzites and metaconglomerates of the Equador Formation. The trace-element ratios in feldspar and micas allow to classify most pegmatites as belonging to the beryl–columbite phosphate subtype. Electron microprobe analyses (EMPA) of columbite, tapiolite, niobian–tantalian rutile, ixiolite and wodginite group minerals from 28 pegmatites in the BPP are used to evaluate the effectiveness of Nb–Ta oxide chemistry as a possible exploration tool, to trace the degree of pegmatite fractionation and to classify the pegmatites. The columbite group mineral composition allows to establish a compositional trend from manganoan ferrocolumbite to manganocolumbite and on to manganotantalite. This trend is typical of complex spodumene- and/or lepidolite-subtype pegmatites. It clearly contrasts with another trend, from ferrocolumbite through ferrotantalite to ferrowodginite and ferrotapiolite compositions, typical of pegmatites of the beryl–columbite phosphate subtype. Large scatter and anomalous trends in zoned crystals partially overlap and conceal the two main evolution patterns. This indicates that a large representative data set of heavy mineral concentrate samples, collected systematically along cross-sections, would be necessary to predict the metallogenetic potential of individual pegmatites. Other mineral species, e.g. garnets and/or tourmaline, with a more regular distribution than Nb–Ta oxides, would be more appropriate and less expensive for routine exploration purposes. The currently available Nb–Ta oxide chemistry data suggest the potential for highly fractionated Ta–Li–Cs pegmatites in the BPP, so far undiscovered, and encourages further, more detailed research.     

Spinels,Fe–Ti oxide minerals,apatites, and carbonates hosted in the ophiolites of Eastern Desert of Egypt: mineralogy and chemical aspects

Spinels, Fe–Ti oxide minerals, apatites, and carbonates hosted in ophiolitic serpentinites and metagabbros of Gabal Garf (southern ED) and Wadi Hammariya (central ED) of Egypt are discussed. Microscopic and electron probe studies on these minerals are made to evaluate their textural and compositional variations. Alteration of chromites led to form ferritchromite and magnetite; rutile–magnetite intergrowths and martite are common in serpentinites. Fine trillis exsolution of ilmenite–magnetite and ilmenite–hematite and intergrowth of rutile–magnetite and ilmenite–sphene are recorded. Composite intergrowth grains of titanomagnetite–ilmenite trellis lamellae are common in metagabbros. The formation of ilmenite trellis and lamellae in magnetite and titanomagnetite indicate an oxidation process due to excess of oxygen contained in titanomagnetite; trapped and external oxidizing agents. This indicates the high P _H2O and oxygen fugacity of the parental magma. The sulfides minerals include pyrrhotite, pyrite and chalcopyrite. Based on the chemical characteristics, the Fe–Ti oxide from the ophiolitic metagabbros in both areas corresponds to ilmenite. The patites from the metagabbros are identified as fluor-apatite. Carbonates are represented by dolomites in serpentinites and calcite in metagabbros. Spinel crystals in serpentinites are homogenous or zoned with unaltered cores of Al-spinel to ferritchromit and Cr-magnetite toward the altered rims. Compared to cores, the metamorphic rims are enriched in Cr# (0.87–1.00 vs. 0.83–0.86 for rims and cores, respectively) and impoverished in Mg# (0.26–0.48 vs. 0.56–0.67) due to Mg–Fe and Al (Cr)–Fe³⁺ exchange with the surrounding silicates during regional metamorphism rather than serpentinization process. The Fe–Ti oxides have been formed under temperature of ~800 °C for ilmenite. Al-spinels equilibrated below 500–550 °C, while the altered spinel rims correspond to metamorphism around 500–600 °C. Geochemical evidence of the podiform Al-spinels suggest a greenschist up to lower amphibolite facies metamorphism (at 500–600 °C), which is isofacial with the host rocks. Al-spinel cores do not appear to have re-equilibrated completely with the metamorphic spinel rims and surrounding silicates, suggesting relic magmatic composition unaffected by metamorphism. The composition of Al-spinel grains suggest an ophiolitic origin and derivation by crystallization of boninitic magma that belonging to a supra-subduction setting could form either in forearcs during an incipient stage of subduction initiation or in back-arc basins.     

Formation,evolution of the granitic complex and its contribution to mineralization in Dongqiyishan deposit,Inner Mongolia: Chronological and geochemical evidencesSCIEI北大核心CSCD

内蒙古东七一山钨多金属矿位于北山造山带东段,是一个以钨为主,共伴生锡、钼、铷、铍、铌、钽、铁和萤石的综合型矿床。本次工作对含矿花岗质杂岩开展了岩石学、地球化学、锆石U-Pb及辉钼矿Re-Os年代学研究。富W-Sn-Mo花岗岩岩性为细粒似斑状二长花岗岩、中细粒似斑状二长花岗岩、花岗斑岩,结晶年龄分别为220.6±1.6Ma、220.4±1.3Ma和220.0±1.1Ma。富Rb-Be-Nb-Ta花岗岩岩性为中粗粒钠长石化似斑状二长花岗岩,结晶年龄为219.9±1.9Ma。辉钼矿Re-Os定年获得加权平均年龄为211±1Ma(MSWD=0.83),说明成岩成矿发生在晚三叠世。含矿花岗质杂岩均具有高硅、富碱、贫铁镁钙特征,为高钾钙碱性花岗岩。其中,富W-Sn-Mo花岗岩为准铝质-过铝质花岗岩;而富Rb-Be-Nb-Ta花岗岩为强过铝质花岗岩。杂岩体轻重稀土具一定分馏,呈现显著的负Eu异常,均富集Rb、K、U、Ta,强烈亏损Ba、Nb、Sr、P、Ti、Zr、Hf。与富W-Sn-Mo花岗岩相比,富Rb-Be-Nb-Ta花岗岩具更低的稀土总量,更显著的Eu负异常,并显示微弱的稀土四分组效应,更高的Li、Ta含量,更低的P、Ti、Zr、Hf、W、Mo、Bi含量。时空关系和地球化学特征表明,杂岩体为同一次岩浆活动不同演化阶段的产物,均经历了较高程度的结晶分异和较强的熔体-流体相互作用。相比而言,富Rb-Be-Nb-Ta花岗岩比富W-Sn-Mo花岗岩结晶分异程度更高,熔体-流体作用更强,花岗质岩浆的高程度分离结晶和熔体-流体相互作用是形成该杂岩体并促使成矿的重要控制因素。     

Magmatic–hydrothermal rare-element mineralization in the Songshugang granite (northeastern Jiangxi,China): Insights from an electron-microprobe study of Nb–Ta–Zr minerals

The Songshugang granite, hidden in the Sinian metasedimentary stratum, is a highly evolved rare-element granite in northeastern Jiangxi province, South China. The samples were systematically taken from the CK-102 drill hole at the depth of 171–423 m. Four types of rocks were divided from the bottom upwards: topaz albite granite as the main body, greisen nodules, topaz K-feldspar granite and pegmatite layer. Electron-microprobe study reveals that the rare-element minerals of the Songshugang granite are very different from those of other rare-element granites. Mn^# [Mn/(Fe + Mn)] and Ta^# [Ta/(Nb + Ta)] of columbite-group minerals and Hf^# [Hf/(Zr + Hf)] of zircon are nearly constant within each type of rocks. However, back-scattered electron imaging revealed that Nb–Ta oxides and zircon of the Songshugang granite, especially those of topaz albite granite, topaz K-feldspar granite and greisen, are commonly characterized by a specific two-stage texture on the crystal scale. The early-stage Nb–Ta oxide is simply subhedral-shaped columbite-(Fe) (CGM-I) with low Mn^# (0.16–0.37) and Ta^# (0.05–0.29). Columbite-(Fe) is penetrated by the later-stage tantalite veinlets (CGM-II) or surrounded by complex Nb–Ta–Sn–W mineral assemblages, including tantalite-(Fe), wodginite (sl), cassiterite, and ferberite. Tantalite has wide range of Mn^# values (0.15–0.88) from Fe-dominance to Mn-dominance. Wodginite with Ta>Nb has large variable concentrations of W, Sn and Ti. Cassiterite and ferberite are all enriched in Nb and Ta (Nb₂O₅ + Ta₂O₅ up to 20.12 wt.% and 31.42 wt.%, respectively), with high Ta^# (>0.5). Similar to Nb–Ta oxides and Nb–Ta–Sn–W mineral assemblages, the early-stage zircon is commonly included by the later-stage zircon with sharply boundary. They have contrasting Hf contents, and HfO₂ of the later-stage zircon is up to 28.13 wt.%. Petrographic features indicate that the early-stage of columbite and zircon were formed in magmatic environment. However, the later-stage of rare-element minerals were influenced by fluxes-enriched fluids. Tantalite, together with wodginite, cassiterite, and ferberite implies a Ta-dominant media. An interstitial fluid-rich melt enriched in Ta and flux at the magmatic–hydrothermal transitional stage is currently a favored model for explaining the later-stage of rare-element mineralization.     

Abundant Fe–Ti oxide inclusions in olivine from the Panzhihua and Hongge layered intrusions, SW China: evidence for early saturation of Fe–Ti oxides in ferrobasaltic magma

Abundant Fe–Ti oxide inclusions in cumulus olivine (Fo_77–81) from the Panzhihua and Hongge intrusions, Emeishan large igneous province, SW China, document the first evidence for early crystallization of Fe–Ti oxides in ferrobasaltic systems in nature. The intrusions also contain significant stratiform Fe–Ti–V oxide ores. The oxide inclusions are sub-rounded or irregular, range from ∼5 to 50 μm in diameter, and are dominated by either titanomagnetite or ilmenite. The fact that the inclusions are either titanomagnetite- or ilmenite-dominant suggests that they are trapped crystals, instead of immiscible oxide melt, formed during growth of the host olivine. The absence of other silicate phases in the inclusion-bearing olivine is difficult to reconcile with a possible xenocrystic origin of the oxide inclusions. These oxide inclusions are thus interpreted to be cumulus minerals crystallized together and trapped in olivine from the same parental magma. In addition to Fe–Ti oxides, some inclusions contain amphibole + biotite ± fluorapatite that might have formed by reaction of trapped hydrous liquid with the host olivine. Numerical modeling of high-Ti Emeishan basalts using the MELTS program successfully simulates early crystallization of olivine (∼Fo₈₁) and Fe–Ti spinel in the presence of a moderate amount of H₂O (∼1.5 wt%) under pressure and fO₂ conditions generally pertinent to the Panzhihua and Hongge intrusions. The modal mineralogy of the oxide inclusions is in good agreement with the bulk compositions of the ore, as inferred from whole-rock data, in a given intrusion. This is consistent with the interpretation that the stratiform oxide ores in the intrusions formed by accumulation of Fe–Ti oxide crystals that appeared on the liquidus with olivine and clinopyroxene.     

Macrocrystic corundum and Fe–Ti oxide minerals entrained in alkali basalts from the Eger (Ohře) Rift: Mg−Fe3+-rich ilmenite as tracer of an oxidized upper mantle

Macrocrysts of corundum, ilmenite, and spinel-group minerals from alluvial deposits of the Eger Rift were studied for composition, texture, and mineral inclusions. All macrocrysts show usually magmatic corrosion textures indicating disequilibrium with the transporting alkali-basalt magma. Corundum grains, exclusively sapphires, were classified by trace-element signatures as magmatic and metamorphic types. Some sapphire grains show erratic compositions that may have resulted from a metasomatic overprint. The inclusion inventory of magmatic corundum suggests crystallization from a differentiated alkaline silicate melt. Corundum itself was never observed as an inclusion mineral. Magnesium- and Fe³⁺-rich ilmenite, described as typical mantle-derived species, is the dominant heavy mineral in almost all alluvial deposits of the Eger Rift. Most discrete macrocrysts are similar in appearance and composition to kimberlite- and basanite-related ilmenite. Ilmenite included in alluvial corundum and zircon grains differ from the bulk of discrete ilmenite grains by larger concentrations of Nb and Mn. The mantle origin of the Mg–Fe³⁺-rich ilmenite is confirmed by compositional and thermo-barometric comparison with ilmenite from clinoproxenitic and hornblenditic xenoliths, which probably originated in the Moho region. The Fe–Ti two-oxide geothermometry and oxygen-barometry of coexisting ilmenite–magnetite pairs yield equilibrium temperatures between 900 and 1,080 °C and oxygen fugacities log₁₀fO₂ between ?0.1 and 1.1 (relative to the NNO buffer), which indicate that the upper mantle as well as the mantle/crust transition zone below the rift is at least partially oxidized. The ilmenite macrocrysts were transported from the source region to the surface by explosive alkali-basalt magmas, as implied by the presence of basaltic-pipe breccias in close vicinity to some placer deposits.     

Fine-particle Mn and other metals linked to the introduction of MMT into gasoline in Sydney, Australia： Results of a natural experiment

PM2.5 particulates were analyzed using accelerator-based ion beam methods for a suite of 21 species （H, C, Na, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Br, Pb） to evaluate the contribution to Sydney air associated with the introduction of MMT as a replacement for Pb. MMT was discontinued in 2004. Teflon filters continuously sampled for 7 years from 1998 to 2004 were analyzed from two sites： a suburb （Mascot） close to the Central Business District [CBD （n=718）] and a high trafficked area, and a relatively rural （background） setting, ～20 km west of the CBD （n=730）. Mean Mn concentrations in air at the background site increased from 1.5- 1.6 ng/m^3 to 〈2 ng/m^3 at the time of the greatest MMT use whereas those at Mascot increased from about 2 to 5 ng/m^3. From the maximum values, the Mn showed a steady decrease at both sites concomitant with the decreasing use of MMT. Lead concentrations in air at both sites decreased from 1998 onwards, concomitant with the phase out of leaded gasoline in 2002. A high correlation was obtained for the relationship between Mn in air and lead replacement gasoline （LRG） use （R2 0.83） and an improved correlation for Mn/Al＋Si＋K and LRG use （R2 0.93）. With Mn concentrations normalized to background values of Al＋Si＋K to account for the lithogenically-derived Mn, the proportion of anthropogenic Mn was -70%. Changes for Mn and Pb in the particulates are attributed to the before-during-after use of MMT and decreasing use of Pb in gasoline.     

The crystal chemistry of lithium in the alluaudite structure: a study of the (Na1− x Li x )1.5Mn1.5Fe1.5(PO4)3 solid solution (x = 0 to 1)

Summary Phosphates of compositions (Na_1–xLi_x)_1.5Mn_1.5Fe_1.5(PO₄)₃ were synthesized by solid state reactions in air, and pure alluaudite-type compounds were obtained for x=0.00, 0.25, and 0.50. Rietveld refinements of X-ray powder diffraction data indicate the occurrence of Mn²⁺ in the M(1) site, and of Fe³⁺ and Mn²⁺ in the M(2) site. For x=0.25 and 0.50, A(1) is occupied by Li⁺ and Na⁺, whereas A(2) is occupied by Na⁺ and vacancies. A careful examination of the number of electrons occurring in the A sites of the alluaudite-type compounds (Na_1–xLi_x)MnFe₂(PO₄)₃ and (Na_1–xLi_x) CdIn₂(PO₄)₃ confirms that lithium occupies only the A(1) crystallographic site of the alluaudite structure.     

New calibration data for the Fe–Ti oxide thermo-oxybarometers from experiments in the Fe–Ti–O system at 1 bar, 1,000–1,300°C and a large range of oxygen fugacities

The current formulations of the Fe–Ti oxide thermobarometer (titanomagnetite–ilmenite_ss) fail to reproduce experimental results, in particular at the high temperatures that are relevant for basaltic assemblages. With the aim of improving the experimental basis of the calibration in the Fe–Ti–O system, we have synthesised assemblages of titanomagnetite–ilmenite_ss (Tmt–Ilm_ss), ilmenite_ss–pseudobrookite_ss (Ilm_ss–Psb_ss) and single-phase samples under a wide range of fO₂ (fixed with CO/CO₂ mixtures or by solid oxygen buffers) in sub-solidus conditions (1,000–1,300°C) at 1 bar. Runs lasted 24 h at 1,300°C and up to 240 h at 1,000°C and were terminated by quenching in water. All run products are polycrystalline, roughly equigranular aggregates, with grain sizes of 10–50 m. They were examined and analysed with the SEM and EMP. Tmt compositions are broadly in accordance with the current models at moderate fO₂, but significantly richer in Ti at low fO₂ and high T, due to cationic vacancies. Ilm_ss compositions depart from the predicted values practically at all fO₂ and T conditions, which is related to unsatisfactory thermodynamic models for the rhombohedral oxide. For Ilm_ss–Psb_ss assemblages the best agreement between our data and current calculations is at 1,000°C and moderately high fO₂. Otherwise, experimental and calculated data strongly disagree. The experimental data set on the three Fe–Ti oxide solid solutions presented here is intended to support new versions of both the titanomagnetite–ilmenite_ss thermo-oxybarometer and the ilmenite_ss–pseudobrookite_ss oxybarometer.     

Recycling of palaeo-Pacific subducted oceanic crust related to a Fe–Cu–Au mineralization in the Xu-Huai region of North Anhui-Jiangsu,East China: Geochronological and geochemical constraints

ABSTRACT

In this study, Early Cretaceous skarn deposits and genesis of their host diorite/monzodiorite porphyry in the Xuzhou-Huaibei (Xu-Huai) region, northern Anhui-Jiangsu have been discussed by detailed geochemical work. In-situ zircon U–Pb dating of the diorites related to Fe–Cu–Au deposits shows that they were formed between 131.4 ± 1.5 Ma and 130.8 ± 1.8 Ma. Geochemical data indicate a depletion of high field strength elements (HFSE) in the diorite porphyry with similarity to that of arc-related igneous rocks. The diorite porphyry was probably derived from typical arc magmas related to continental margin subduction characterized by light rare earth elements (LREEs) enrichment and HFSE depletion. REEs compositions of apatite in the diorite porphyry indicate that the dioritic magma was produced from the metasomatized subcontinental mantle by slab-derived fluids. The magma was proven to be a high oxygen fugacity; thus, it was particularly conducive to the precipitation of Fe, Cu, Au and other ore-forming elements. The δ³⁴S values of pyrite and chalcopyrite of Fe–Cu–Au ores range from ?0.2‰ to 2.8‰, indicating that the sulphur in the ore was probably derived from deep-seated magmas. Integrated with geochronological and geochemical analyses, we suggest that the Early Cretaceous igneous suites associated with Fe–Cu–Au deposits in the Xu-Huai region are related to recycling subduction of Pacific oceanic crust.     

A combined EMPA and LA-ICP-MS study of Li-bearing mica and Sn–Ti oxide minerals from the Qiguling topaz rhyolite (Qitianling District,China): The role of fluorine in origin of tin mineralization

The Sn-rich Qiguling topaz rhyolite dike intrudes the Qitianling biotite granite of the Nanling Range in southern China; the granite hosts the large Furong Sn deposit. The rhyolite dike is typically peraluminous, volatile-enriched, and highly evolved. Whole-rock F and Sn concentrations attain 1.9 wt.% and 2700 ppm, respectively. The rhyolite consists of a fine-grained matrix formed by quartz, feldspar, mica and topaz, enclosing phenocrysts of quartz, feldspar and mica; it is locally crosscut by quartz veinlets. Lithium-bearing micas in both phenocrysts and the groundmass can be classified as primary zinnwaldite, “Mus-Ann” (intermediate member between annite and muscovite), and secondary Fe-rich muscovite. Topaz is present in the groundmass only; common fluorite occurs in the groundmass and also in a specific cassiterite, rutile and fluorite (Sn–Ti–F) assemblage. Cassiterite and rutile are the only Sn and Ti minerals; both cassiterite and Nb-rich rutile are commonly included in the phenocrysts. The Sn–Ti–F assemblage is pervasive, and contains spongy cassiterite in some cases; cassiterite also occurs in quartz veinlets which cut the groundmass. Electron microprobe and LA-ICP-MS compositions were used to study the magmatic and hydrothermal processes and the role of F in Sn mineralization. The presence of zinnwaldite and “Mus-Ann”, which are respectively representative of early and late mica crystallization during magma differentiation, also suggests a significant decrease in f(HF)/f(H₂O) of the system. Cassiterite included in the zinnwaldite phenocrysts is suggested to have crystallized from the primary magma at high temperature. Within the Sn–Ti–F aggregates, rutile crystallized as the earliest mineral, followed by fluorite and cassiterite. Spongy cassiterite containing inclusions of the groundmass minerals indicate a low viscosity of the late fluid. The cassiterite in the quartz veinlets crystallized from low-temperature hydrothermal fluids, which possibly mixed with meteoric water. In general, cassiterite precipitated during both magmatic and hydrothermal stages, and over a range of temperatures. The original fluorine and tin enrichments, f(HF)/f(H₂O) change in the residual magma, formation of Ca,Sn,F-rich immiscible fluid, decrease of the f(HF) during groundmass crystallization, and mixing of magma-derived fluids with low-saline meteoric water during the late hydrothermal stage, are all factors independently or together responsible for the Sn mineralization in the Qiguling rhyolite.     

Interstitial water – sediment geochemistry of N, P and Fe and its response to overlying waters of tropical estuaries: a case from the southwest coast of India

 The concentrations of N, P and Fe in surface sediments and interstitial and overlying (bottom and surface) waters of the Ashtamudi estuary located in the southwest coast of India are reported along with the various chemical species of N (NO₂–N, NO₃–N, NH₃–N and total N) and P (organic P, inorganic P and total P) in interstitial and overlying waters and discussed in terms of the physico-chemical environment of the system. The interstitial water exhibits higher salinity values compared to bottom and surface waters, indicating the coupled effects of salt-wedge phenomena and gravitational convection of more saline-denser marine water downward through surface sediments. N, P and Fe as well as their chemical forms are enriched in the interstitial water compared to bottom and surface waters. However, the dissolved oxygen (DO) shows an opposite trend. The marked enrichment of NH₃–N in the interstitial water and its marginal presence in bottom and surface waters, together with the substantial decrease in the DO concentrations of bottom water and consequent increase in the concentrations of NO₂–N and NO₃–N in interstitial and bottom waters, points to the nitrification process operating in the sediment-water interface of the Ashtamudi estuary. The enrichment of total N, P and Fe in the interstitial water compared to the overlying counterparts and the positive correlation of sediment N, P and Fe with mud contents as well as organic carbon indicate that these elements are liberated during the early diagenetic decomposition of organic matter trapped in estuarine muds. Received: 5 Oktober 1998 · Accepted: 9 February 1999     

From land to sea: provenance,composition, and preservation of organic matter in a marine sediment record from the North-East Greenland shelf spanning the Younger Dryas–Holocene

The organic matter content of marine sediments is often used to infer past changes in ocean conditions. However, the organic carbon pool preserved in coastal sediments is a complex mixture derived from different sources and may not reflect in situ processes. In this study, we combine taxonomic identification of reworked palynomorphs with pyrolysis organic geochemistry and reflected-light organic petrographic microscopy to investigate the provenance, composition and preservation of organic matter in a marine sediment core retrieved from the NE Greenland shelf. Our study reveals continuous yet variable input of land-derived organic carbon to the marine environment throughout the late Younger Dryas–Holocene, with the highest input of inert carbon in the late Younger Dryas. Although the sediments contain some recent marine palynomorphs, there is no other evidence of fresh marine organic carbon. In contrast, our results indicate that these shelf sediments represent a significant sink of recycled organic carbon. The results of pyrolysis geochemistry revealed that ~90% of the total organic carbon in the sediments is inert. The organic petrography analyses revealed that >70–84% of the organic carbon in the sediment core is terrigenous. Reworked dinoflagellate cysts showed a continuous provenance of Cretaceous land-derived material, most likely from the nearby Clavering Island. Our study points to the importance of constraining the organic matter origin, composition and preservation in marine sediments to achieve more accurate palaeoenvironmental reconstructions based on organic proxies.     

Solubility of columbite, (Mn,Fe)(Nb,Ta)<Subscript>2</Subscript>O<Subscript>6</Subscript>, in granitoid and alkaline melts at 650–850°C and 30–400 MPa: An experimental investigation

This paper reports experimental data on columbite solubility in model water-saturated Li- and F-rich silicic melts with different contents of alumina and alkalis. It was found that the columbite solubility is strongly affected by melt composition and is maximal in peralkaline melt. The maximum contents of Ta and Nb in subaluminous and peraluminous melts at the contact with columbite are lower by at least an order of magnitude. The peralkaline melt is relatively enriched in Nb, and the peraluminous melt is enriched in Ta. The temperature dependence of solubility is positive but less pronounced than the effect of melt composition. It is most distinct in the subaluminous melts. The Nb/Ta ratio of melt usually decreases with decreasing temperature. The effect of pressure is relatively small. It was shown that columbite cannot crystallize on the liquidus of both peralkaline and peraluminous magmas. Perhaps, columbite crystallization from a melt is possible only at final near-solidus stages at the high degrees of crystallization of strongly evolved low-temperature melts.     

The role of recycled oceanic crust in magmatism and metallogeny: Os–Sr–Nd isotopes, U–Pb geochronology and geochemistry of picritic dykes in the Panzhihua giant Fe–Ti oxide deposit, central Emeishan large igneous province, SW China

The picritic dykes occurring within fine-grained gabbro in the marginal zone and in the surrounding Proterozoic wall-rock marbles of the Panzhihua Fe–Ti oxide deposit closely correspond in bulk composition with the nearby Panzhihua intrusion. These dykes offer important constraints on the nature of the mantle source of the Panzhihua ore-bearing intrusion and its possible link to the Emeishan plume. U–Pb zircon dating of the picritic dyke yields a crystallization age of 261.4 ± 4.6 Ma, coeval with the timing of the main Panzhihua gabbroic intrusion and Late Permian Emeishan flood basalts. The Panzhihua picritic dykes contain 37.63–43.41 wt% SiO₂, 1.15–1.56 wt% TiO₂, 11.43–13.25 wt% TFe₂O₃, and 20.96–28.87 wt% MgO. Primitive-mantle-normalized patterns of the rocks are comparable to those of ocean island basalt. The rocks define a relatively small range of Os isotopic compositions and a low Os signature of ?0.13 to +2.76 for γ_Os (261 Ma). In combination with their Sr–Nd–Os isotopic compositions, we interpret that these rocks were derived from the Emeishan plume sources as well as the interactions of plume melts with the overlying lithosphere which had been extensively affected by eclogite-derived melts from the deep-subducted oceanic slab. Partial melting induced by an upwelling mantle plume that involved an eclogite or pyroxenite component in the lithospheric mantle could have produced the parental Fe-rich magma. Our study suggests that plume-lithosphere interaction might have played a key role in generating many world-class Fe–Ti oxide deposits clustered in the Panxi area.     

Regional metamorphism and the alteration response of selected Silurian to Devonian mineral systems in the Nymagee area,Central Lachlan Orogen,New South Wales: a HyLogger™ case study

The southern Cobar Superbasin includes the Mount Hope, Cobar and Rast troughs and adjacent Winduck, Mouramba and Kopyje shelves. These stratotectonic units host a range of mineral systems within deformed upper Silurian to Lower Devonian rocks. Despite the metallogenic importance of the terrane the regional metamorphic- and alteration-related mineral assemblages have not been systematically described until now. Here, we present a study using the HyLogger? spectral scanner to systematically map changes in both background and alteration-related mineralogy for 14 mineral systems across the Nymagee area. The study found that, with the exception of the late diagenetic zone assemblages associated with the Winduck Shelf, the mineral assemblages for zones away from mineralisation are consistent with uniform sub- to lowest-greenschist facies metamorphic conditions, with no evidence for a regional, thermal field gradient across the basin. By contrast, proximal to mineralisation, there are significant changes in alteration-related mineral abundances and species reflecting elevated fluid temperatures. For several zones, including Browns Reef, Great Central, Hera, May Day, Nymagee and Shuttleton, there is a systematic change in chlorite composition from Fe- and/or Fe–Mg-chlorites to more Mg-rich varieties towards mineralisation. In addition, talc was noted for May Day, Mineral Hill and Shuttleton. The change in chlorite composition suggests that these ore-forming fluids were undersaturated with respect to iron. Furthermore, although present in discrete zones, carbonate alteration is not a dominant alteration type. However, at Manuka and Blue Mountain, the mineralisation is associated with carbonate-rich (calcite, ankerite, dolomite) units that have been dolomitised (Mg alteration) but not all dolomite-rich zones are mineralised. For Mineral Hill, there are systematic changes to mineral species/chemistry with observed data consistent with Parkers Hill being proximal to the centre of a mineralising system. The G and H Lode area (Southern Ore Zone) is slightly more distal whereas the Pearse deposit may represent a zone more distal again.     

Clay minerals in sediments of Portuguese reservoirs and their significance as weathering products from over-eroded soils: a comparative study of the Maranhão, Monte Novo and Divor Reservoirs (South Portugal)

The Southern region of Portugal is subjected to several forms of over-erosion. Most leached products, mainly composed of fine particles containing nutrients, metals or pesticides, are easily transported by river flows. When these are hindered by a physical barrier such as a dam, the particulate load accumulates on the bottom of the reservoirs, often leading to a pronounced decrease of water quality. Bottom sediments from three reservoirs were subjected to grain-size analysis and a study of clay minerals by X-ray diffraction. Most sediments contain a diverse set of clay minerals, mostly illites, smectites, chlorites and kaolinites. The nature of the clay minerals reflects the nature of the parent rocks. During the cycles of transport and temporary deposition, they may undergo significant chemical and physical transformations, which lead to an increase of expandable properties and therefore, to a higher cationic exchange capacity, determining its important role as vehicles of environmental pollutants.     

From cave geomorphology to Palaeolithic human behaviour: speleogenesis,palaeoenvironmental changes and archaeological insight in the Atxurra-Armiña cave (northern Iberian Peninsula)

A detailed geomorphological study was performed in the Atxurra-Armiña cave system (northern Iberian Peninsula) to decode landscape evolution, palaeoenvironmental changes and human use of a cave within an Inner Archaeological Context. The results show an average incision rate of the river of <0.083 mm a^–1 for at least the last 419 ka, with interruptions due to sedimentary inputs. Moreover, allostratigraphic units comprising fluviokarstic deposits at the base and flowstone formation at the top have been shown to be climatically controlled, formed either during glacial–interglacial cycles or during interstadial cycles. Finally, when the cave was used by humans in the Late Magdalenian, the lower entrance was closed, and they must therefore have entered the cave through the upper entrance. To reach the sectors selected to decorate the panels, they probably travelled from the upper cave level, as the current crawlway was wider than today, according to our U/Th dating. Once these visitors reached the panels, the floor in the main gallery would have been around 15 cm lower than at present. However, the morphology of the conduit was similar; this has significant implications for understanding and interpreting the human use of the cave during the Palaeolithic.