Premetamorphic lateritisation in Proterozoic metabasites of Rogaland,SW Norway

Heterogeneous layers of granulite facies metamorphic basites of the Proterozoic supracrustal Faurefjell Formation in Rogaland, S.W. Norway, display an extreme chemical variation. Within a single layer the bulk chemical composition gradually changes from approximately basaltic in basic granulites to alumina-iron-rich in granofelses. Component-ratios and composition-volume relations indicate open-system chemical reactions mainly involving the extraction of silica. Apparent enrichment in Fe, Ti, P, Al, Zr, Ni, Co, Zn, Y, Nb, Hf and REE and variations in resulting metamorphic mineral assemblages are related to premetamorphic progressive lateritisation of a basaltic protolith. The weathering generated a continuous chemical suite from SiO₂=48 wt%, Fe₂O₃=10 wt% and Al₂O₃=19 wt% in the basic granulites to 14 wt%, 40 wt% and 25 wt% in the Fe-Al granofelses. Metasomatism during diagenesis and during (very) high-grade metamorphism (1200–900 Ma) further perturbed the concentrations of relatively mobile elements Ca, Mg, K, Rb, Sr, Ba, Na and Li in the laterites without affecting the transition metal ratios. In particular, the REE did not fractionate differentially during the supracrustal and metasomatic alteration.     

Petrogenesis of the Concordia Granite Gneiss and its relation to WMo mineralization in western Namaqualand, South Africa

The 1.1 Ga Concordia Granite Gneiss (CGG) is part of the late to postorogenic Spektakel Suite in the western Namaqualand Metamorphic Complex, South Africa. It intruded synkinematically, with respect to the main (D2) deformation event, into lower to middle crustal rocks and granite emplacement was more or less coeval with the peak of granulite-facies metamorphism ( > 800°C, 5 kbar). Several genetically related rock types, megacrystic garnet-bearing granite, minor aplitic leucogranites and pegmatites are distinguished. All varieties are SiO₂-rich (69–79 wt.%) peraluminous granites and show subalkaline-monzonitic magma characteristics. Geochemical differences in whole-rock chemistry between megacrystic granite and aplitic leucogranites (e.g., lower Al₂O₃, MgO, CaO, Ba, Zr; higher K₂O, Rb, Nb, W, Rb/Sr, Ga/Al) and the decrease of e.g., CaO, MgO, Fe₂O₃, Ba, Zr, Th/U with increasing SiO₂ in the megacrystic granites as well as the variation in Fe/Mn of magmatic garnets are best explained with crystal fractionation processes. Fractional crystallization of plagioclase produced potassium- and silica-rich residual melts characterised by very high Rb/Sr, Rb/Ba, U/Th, Mn/Fe ratios and higher concentration of W, Cu and Zn. Crystal fractionation processes also resulted in a relative LREE depletion and HREE enrichment (megacrystic granite: La/Lu)_cn = 8.87−31.67; aplitic leucogranite and pegmatites: La/Lu)_cn = 0.71−1.44) and evolution of pronounced negative Eu-anomalies. The crystallization sequence (near-solidus crystallization of biotite prior to alkali feldspar) suggests that the CGG magmas were H₂O-undersaturated over a long period of their evolution. Water saturation during late-stage crystallization is, however, indicated by coarse late-stage eutectic mineral textures, pegmatites and WMo-bearing siliceous rocks. Furthermore the economic potential of the CGG is supported by its geochemical signature (e.g., high U, Th contents) which is similar to evolved high heat production (HHP) granites. The granitic magmas are attributed to partial melting of peraluminous crustal source rocks and are tentatively interpreted as fractionated S-type granites. The WMo deposits represent vein-type and pegmatitic deposits genetically related to a deep-seated granitic system.     

Alkaline and calc-alkaline lavas near Los Volcanes,Jalisco, Mexico: geochemical diversity and its significance in volcanic arcs

A remarkably diverse suite of lavas erupted during the late-Pliocene at the volcanic front of the western Mexican Volcanic Belt near the town of Los Volcanes, Jalisco. This region is much closer to the Middle America Trench than the main axis of Quaternary andesite-dacite stratovolcanoes, and volcanism occurred in a complex tectonic regime involving both subduction of the young Rivera Plate and transverse crustal extension of the Jalisco structural block. The variety of lava types covers a wide spectrum from highly potassic minettes and leucitites to calc-alkaline basalts and andesites which are compositionally similar to those erupted elsewhere in the Mexican Volcanic Belt. Other alkaline varieties intermediate between these extremes include absarokites, trachybasalts and trachyandesites. Phlogopite, amphibole and apatite are common phenocryst phases; whole-rock compositions show a wide range of alkali contents (e.g. K₂O of 1.0–8.6 wt.%), and typically contain >5 wt.% MgO. MgO, Ni, V and Cr show little systematic decrease with increasing SiO₂, suggesting that these lavas have evolved from primitive, mantle derived magmas with a wide range of SiO₂ contents. Strong enrichments in incompatible trace elements are observed in all of the lavas (Sr 700–5100 ppm, Ba 470–4800, Ce 22–325 ppm, Zr 90–700 ppm), as is the relative enrichment of large ion lithophile (Ba, Sr, Rb) and light rare-earth elements (La, Ce) over the high field strength elements (Ti, Zr) which is typical of magmas in volcanic arcs. This enrichment pattern suggests that these magmas come from source regions which contain incompatible element-rich phases such as phlogopite, amphibole and apatite. The petrological and geochemical features of the lavas which occur in the Los Volcanes region provide direct evidence of the extreme heterogeneity which may exist in magma source regions at convergent margins. The complex tectonic regime in western Mexico further suggests that rifting and crustal extension play an important role in the generation and successful ascent of melts from enriched regions of the sub-arc mantle.     

Petrogenesis of fractionated basaltic lava flows of Poladpur-Mahabaleshwar formation around Mahabaleshwar,Western Ghats,India

Geochemical investigations of Wai sub-group volcanic flows (in and around Mahabaleshwar) have been undertaken to determine the petrogenetic processes involved in the formation of volcanic flows. In comparison to the Ambenali Formation, Mahabaleshwar Formation flows were affected more by crustal materials, which left a signature consisting of enriched levels of K, Rb, Ba, Ti and P. Ratios of Nb/Zr and Ba/Y were sensitive to fractional crystallization; Mahabaleshwar formation flows showed the highest Nb/Zr ratios. Ba was noted as a boundary marker element between the Ambenali (47.3 to 63.9 ppm Ba) and Mahabaleshwar (83.1 to 180 ppm) formations. The general trend of incompatible element concentrations increasing from lower Poladpur to upper Mahabaleshwar flows with increasing Zr and the linear array on the plot are consistent with the fractionation of olivine and clinopyroxene. MgO ranged from 4.8 to 7.1 wt%, TiO₂ from 1.8 to 4.6 wt%, SiO₂ from 47 to 52 wt% and Al₂O₃ from 12 to15.5 wt%. The Mg number (Mg#) was much lower, ranging from 36 to 50. The K₂O/ P₂O₅ ratio showed the role of assimilation in the basaltic flows. TiO₂, Y, Zr, Nb and Mg# were used to determine fractional crystallization, whereas Ba, Rb, K₂O and SiO₂ were used for monitoring the fractional crystallization effects of crustal contamination. The range of Zr/Y and TiO₂ > 1.8 wt% appears to have been generated by fractional crystallization starting from enriched mafic precursors.     

Geochemistry of micas from the Finero spinel-lherzolite,Italian Alps

The Finero lherzolite is distinct amongst the tectonically emplaced slices of mantle in the Ivrea Zone (Italian Alps) for its abundant coarse phlogopite. An average composition (SiO₂ 39.9, TiO₂ 0.97, Al₂O₃ 16.0, Cr₂O₃ 1.16, FeO 2.73, MgO 24.5, NiO 0.16, BaO 0.31, Na₂O 0.58, K₂O 8.7, Rb₂O 0.056, Cl 0.03, F 0.10 wt.%) is similar in Fe, Cr, Ni, Ba and F/Cl to primary-textured micas from coarse garnet-lherzolite xenoliths from S. Africa, but is higher in Ti, Na, Rb, and Al, and lower in halogens. The distinct values of Ti and Fe for five specimens of Finero peridotites demonstrate local spatial variation. The overall ranges of TiO₂ (0.5–1.7) and FeO (2.3–3.6) fall within the range for secondary-textured micas in peridotite xenoliths from S. Africa. The Finero micas are lower in both K/Rb and K/Ba than the primary and secondary micas from S. Africa, and their mean values of K/Rb (110–220) and K/Ba (15–39) are lower than for almost all bulk rocks, but fit well with the ranges of 109–180 and 12–49 for the high-K lavas of the Roman region.Although all evidence is indicative rather than conclusive, the chemical properties of the Finero micas are consistent with introduction of an alkaline phase into peridotite during or before emplacement of the Finero complex from the upper mantle into the crust, and the coarse, partly-deformed textures can be explained by incomplete metamorphic equilibration during prolonged deformation. The alkaline phase is tentatively attributed to the uppermost mantle.     

Petrogenetic reconnaissance investigation of mafic sills associated with flood basalts,Mekelle basin,northern Ethiopia: implications for Ni–Cu exploration

Mafic sills of the Mekelle basin were explored on a reconnaissance level for their magmatic sulphide potential. The sills are related to Oligocene flood basalt magmatism in Ethiopia. They intrude Jurassic shales and limestones and crystallized from high-Ti tholeiitic basalt magmas. Three compositional groups were differentiated. Among them GD1 gabbrodolerites (11.6–4% MgO) show evidence of a fractionation controlled magmatic lineage, while GD2 (∼5.2% MgO) and GD3 gabbrodolerites (5.4–3% MgO) show element depletion and enrichment patterns which deviate from the magmatic fractionation trend. Compared to GD1 rocks with MgO values ∼5%, GD2 gabbrodolerites have higher SiO₂ and Na₂O but lower FeO_tot, TiO₂, P₂O₅, Nb, Zr, Y, Cu, and Ni values, while GD3 gabbrodolerites show higher SiO₂, Na₂O, P₂O₅, Ba and Sr and lower FeO_tot, TiO₂, Nb, Zr, Y, Cu, and Ni values. The distinct geochemical signatures of the latter two gabbrodolerite groups are likely caused by conjunct processes of crustal assimilation and fractional removal of silicate/oxide mineral phases. Depletion of chalcophile elements in the contaminated gabbrodolerites indicates also the segregation of Ni and Cu sulphides. However, settling of sulphide minerals occurred prior to sill emplacement probably in a deeper seated magma chamber. The indication of chalcophile element depleted mafic sills, genetically related to a major flood basalt province clearly warrants further exploration in the area.     

Metabasalts and metagabbros from the Llano Uplift,Texas: Petrologic and geochemical characterization with emphasis on tectonic setting

The 1.0-1.2 b.y. old rocks of the southeastern Llano Uplift, Texas include a 7 km thick sequence of amphibolite-grade, stratified, mafic metasedimentary rock (Packsaddle Schist) which is intruded by a varied suite of syntectonic and late-kinematic intrusions. The metasediments contain large blocks of serpentinized peridotite (Coal Creek serpentinite) and coarse hornblendite and metagabbro. Prior to the end of maximum deformation, the sequence was intruded by low to medium-K₂O tholeiitic basalts (0.40-0.72% K₂O). Late-kinematic low-K₂O tholeiitic basalts (0.38-0.40% K₂O) were intruded as dikes into the folded rocks. The Coal Creek serpentinite contains both syntectonic and late-kinematic low-K₂O tholeiitic metabasalts (0.13–0.36% K₂O). The Llano metabasalts and metagabbros are characterized by low Cr (67–378 ppm) and Ni (36–170 ppm), variable Rb (1.5–14.7 ppm), Sr (140–1229 ppm), TiO₂ (0.40–2.20%), P (568–2707 ppm), and Zr (18–230 ppm), and Y (16–45 ppm), Co (40–57 ppm), and Sc (36–49 ppm) similar to modern MORB. The metabasalts have La abundances from 7 to 39 times chondritic and exhibit light REE enrichment with ¦La/Sm¦_N from 1.13 to 1.45 and ¦La/Yb¦_N from 1.12 to 2.99. The metabasalts show a strong correlation of increasing Zr, Ti, and Y and decreasing Eu/Eu^* (1.56–1.00), CaO/TiO₂, Al₂O₃/TiO₂, and MgO/ MgO+FeO^* with increasing REE enrichment (La_N). The Llano metabasalts and metagabbros have initial ⁸⁷Sr/⁸⁶Sr=0.7029±0.0001. A likely petrogenetic model for these metabasalts is an island arc in which events from early arc development to final late-kinematic intrusion were dominated by tholeiitic volcanism and intrusion. The chemical systematics of the Llano mafic metaigneous rocks suggest they are products of fractionation of olivine, clinopyroxene, and plagioclase from more primitive basaltic magmas generated beneath the island arc complex.     

东昆仑东段清水泉辉长岩体LA-ICP-MS锆石U-Pb年龄、地球化学特征及其构造意义

清水泉辉长岩体位于东昆仑中缝合带清水泉蛇绿岩北侧,主要岩性为角闪辉长岩。该岩体的LA-ICP-MS锆石U-Pb测年结果为452.1±5Ma,形成时代为晚奥陶世。辉长岩体样品SiO_2含量为43.89%~45.99%,Na_2O含量为1.30%~2.32%,K_2O含量为0.68%~1.39%,P_2O_5含量为0.26%~0.40%,TiO_2含量较低,为0.74%~0.95%,MgO含量为5.72%~6.54%,Mg~#值较低,为53~54。岩石地球化学特征显示,该岩体属于拉斑玄武岩系列,稀土元素表现出轻稀土元素富集、重稀土元素亏损的特点,微量元素以富集大离子亲石元素(Cs、Rb、Ba等,尤其以Ba的正异常最为突出)、亏损高场强元素(Nb、Ta、Ti、Zr、Hf)为特征。微量元素构造判别显示,其形成于活动陆缘岛弧构造环境。结合区域地质资料研究表明,清水泉辉长岩体可能形成于以清水泉蛇绿岩为代表的东昆仑中弧后有限洋盆向北俯冲的初始阶段。     

Geochemistry and petrogenesis of acid volcano-plutonic rocks of the Siner area, Siwana Ring Complex, Northwestern Peninsular India

Petrochemical studies on acid plutonic (granite, microgranite) and volcanic (rhyolite, trachyte) rocks occurring in the Siner area of the Siwana Ring Complex, Malani Igneous Suite have been carried out. These rocks are characterized by high concentrations of SiO₂, Na₂O, K₂O, Zr, Nb, Y and REE (except Eu) but low in MgO, Fe₂O₃(t), CaO, Cr, Ni, Sr; indicating their A-type affinity. Field studies in conjunction with the geochemical characteristic indicate that the magmatism in the Siner area is generally represented by peralkaline suite of rocks which are formed due to rift tectonics. It is also suggested that these acidic rocks could have been derived by low degree partial melting of crustal material. Characteristics of certain pathfinder elements such as Rb, Ba, Sr, K, Zr, Nb, REE and the ratios of K/Rb, Zr/Rb, Ba/Rb along with the multi elemental primitive mantle normalized spidergrams suggest that the Siner peralkaline granites and microgranites have the potential for rare metal and rare earth mineralizations.     

Petrology and geochemistry of greywackes from Goa-Dharwar sector,western Dharwar Craton: Implications for volcanoclastic origin

Late Archaean Supracrustals of the Goa-Dharwar sector (GDS) are composed of a thick sequence of greywacke sequence with narrow intercalations of quartzite, BIF and carbonates. Mafic volcanics occupy the base of the sequence. The greywackes are predominantly tuffacious containing chlorite-sericite and hornblende. Arkosic variations containing biotite dominate the western part of the sector. Fine-grained variations occur as isolated narrow lenses within other types of greywackes. The conglomeratic greywackes are localized along the western and the eastern margins of the sector. All of the greywackes are all typically immature containing coarser clasts of mostly plagioclase (18–23%) and quartz (32–34%). Lithic fragments of felsic volcanic rocks are common. The matrix is dominated by mafic material. Biotite and amphibole are related to metamorphic recrystallization. Chlorite, sericite, epidote, carbonate and chert are products of the interplay of diagenesis and low-grade metamorphism. Fe-Ti oxide, sphene, apatite and zircon are usual accessories. But for slight enrichment in K₂O, the major element chemistry of the GDS greywackes is similar to the chemistry of Late Archaean greywackes. They also compare in respect of V, Co, Hf contents, K₂O/Na₂O, SiO₂/Al₂O₃, Na₂O/Al₂O₃, Ba/Rb, Th/U, La/Th, Sm/Nd ratios, steep REE patterns with distinct LREE enrichment and HREE depletion. The GDS greywackes however are distinctly enriched in Rb, Ba, Sr, Th, U, Cu, Zr, Ce/Ce* and depleted in Cr, Ni, and Zn. The conglomeritic and biotite bearing verities contain considerable proportions of clasts derived from the basement tonalitic/granitic terrain. The common tuffacious greywackes containing hornblende and biotite-sericite however include only volcanic clasts and bear evidence of derivation from submarine weathering of predominantly felsic volcanics erupted on a large scale to form a magmatic arc in the later stages of geosynclinal deposition. Geochemical data suggest that the GDS greywackes were laid down in progressively changing basin geometry from a passive to active continental margin and island arc setting.     

Petrology of Serra Geral (Paraná) continental flood basalts,southern Brazil: crustal contamination,source material,and South Atlantic magmatism

The Serra Geral (Paraná) continental flood basalt (SG-CFB) province in Brazil is associated with the Jurassic-Cretaceous breakup of Gondwanaland and the transition of continental to oceanic magmatism during the opening of the South Atlantic Ocean. A suite of 24 samples representative of the SG-CFB in Rio Grande do Sul, southern Brazil, shows a compositional continuum from basalt (50–53 wt% SiO₂, Mg# 60-45), to basaltic andesite, to andesite, rhyodacite, and rhyolite (73 wt% SiO₂). Certain compositional aspects of the mafic rocks (e.g., TiO₂, K₂O, CaO, Zr/Nb, Zr/Y, Ti/Zr) resemble those of basaltic dikes and flows associated with the opening of the North Atlantic Ocean.Fractionation trends are apparent in MgO variation diagrams and calculations show that basalt-basaltic andesite continuums are largely due to removal of plagioclase and clinopyroxene. These mafic rocks can be categorized as (i) having higher or lower incompatible-element contents (e.g. K₂O 0.6–1.5 wt%; Rb 12–43 ppm; Ba 125–240 ppm) due to incorporation of Brazilian Archean crust or rhyolitic magma by basalt from a particular source material or to partial-melting differences of that source, and (ii) as having higher or lower TiO₂, Sr, Ba, and P contents due to source heterogeneities. Crustal components are obvious in certain basaltic samples, as where K₂O > 1 wt%, SiO₂ > 51%, and TiO₂ 1%, but are insignificant in others (e.g., compositions close to those of South Atlantic basin basalts). Calculations indicate origins for intermediate and silicic rocks by removal of pl, cpx, and Ti-magnetite from basaltic andesite, but crust and magma-mixing affecting basaltic-andesite fractionates were likely also involved. Where contamination is insignificant, Zr, Nb, and Y abundances indicate T-type MORE source material like that for certain S. Atlantic Ocean basalts. Source material was essentially a 91 hybrid of N-type and P-type MORB components. N-type MORB lithosphere followed SG-CFB because decompression due to rifting crust enabled partial melting of uppermost (depleted) mantle.     

Geochemistry and Petrogenesis of the Proterozoic Bandal Mafic Rocks,Himachal Pradesh,NW Himalaya

The Proterozoic Bandal mafic rocks, exposed in Kullu-Rampur window, Lesser Himalaya, Himachal Pradesh, indicate two distinct (high-Ti and low-Ti) magma types. The high-Ti basalts are characterised by high-TiO₂ (> 2 wt%), Ti/Y, Ti/Zr, TiO₂/K₂O and low Rb/Sr ratios. They are enriched in high field strength (HFS) elements (Nb, Zr, Ti) relative to low field strength (LFS) incompatible elements (K, Rb). The low-Ti basalts are charactersied by low TiO₂ (< 2 wt%), Ti/Y, Ti/Zr and high Rb/Sr and Rb/Ba ratios. Quartz-normative composition, continental tholeiite characteristics with Nb/La less than 1 are some of the common factors of the two groups of the Bandal mafic rocks. The trace element concentrations and their ratios of the two groups of the basalts indicate that they have been derived from the asthenosphere at different depths, low-Ti at shallow and high-Ti at deeper levels. Some of the chemical features like low Mg #, Cr, Ni, high incompatible element concentrations (especially Ba), light rare earth element (LREE) enriched patterns point towards assimilation and fractional crystallisation (AFC) process which may have played a significant role in the generation of these basalts.Furthermore, the Bandal mafic rocks, apart from field settings, are geochemically similar to other Proterozoic mafic bodies like the Rampur volcanics, Mandi-Darla volcanics, Garhwal volcanics and Bhimtal-Bhowlai volcanics of the Lesser Himalaya. This widespread Proterozoic continental tholeiitic magmatism over an area of 170,000 km² in the Lesser Himalaya provides an evidence of plume activity in the region.     

Wavelength-dispersive X-ray fluorescence spectrometric determination of Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites

Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours.     

Environmental conditions inferred from multi-element concentrations in sediments off Cauvery delta,Southeast India

We present multi-element concentrations in the surface sediments from the offshore of Cauvery delta of southeast India to evaluate the impact of coastal pollution on the geochemical behaviour of surface deposits. For this study, 16 surface sediment samples were collected from the offshore of Cauvery delta of southeast India and were analysed using traditional XRF for various major (SiO₂, Al₂O₃, MgO, Fe₂O₃, MnO, Na₂O, K₂O, CaO, P₂O₅, TiO₂) and trace elements (Rb, Sr, Ba, Y, Zr, Nb, V, Cr, Co, Ni, Cu, Zn, Th, Pb) after powdering it to ASTM 230 (<63 μm). The main objectives of this study were to understand the geochemical behaviour of the coastal surface sediments and its performance and relation with the pollution indices and statistical analysis. To meet out the objective, pollution indices such as enrichment factor (EF), contamination factor (CF) and Geoaccumulation Index (I _geo) were calculated and statistical analyses were performed to understand the relationship between the geochemical parameters. Both EF and I _geo show the enrichment of Cu, Cr and Zr, whereas CF shows enrichment of Cu and Cr. Statistical analyses exhibit poor correlation between these elements and fine fraction indicating the insignificant role played by both grain size and organic matter. Strong positive association between Cu and Zn with CaCO₃ exhibits the role of carbonates in precipitating these metals from the overlying water column possibly related to agricultural pollution. Distribution and association of other elements suggest the influence of mineralogy in geochemical composition of surface sediments. Based on this study, we suggest that environmental indices alone should not be considered for evaluating environmental conditions and a prior geogenic characterisation of the sediments is necessary.     

Shoshonitic and alkaline lamprophyres with elevated Au and PGE concentrations from the Kreuzeck Mountains,Eastern Alps,Austria

Summary Amphibole and mica lamprophyres and related dykes of Tertiary age from the Kreuzeck Mountains, Central Alps, Austria, have been investigated petrographically and geochemically. They intrude a sequence of early Palaeozoic metapelites, greenstones and amphibolites to the north of the Cretaceous Periadriatic Lineament, a major suture zone of 700 km E-W extent. The dykes are spatially associated with Sb, W, Hg, and Cu-Ag-Au deposits.Most lamprophyres are characterized by primitive chemistry (mg-numbers > 60 and Cr > 200 ppm) and have high contents of LIL elements (K, Rb, Sr and Ba). Geochemically, five different subgroups of calcalkaline/shoshonitic to alkaline affinity can be distinguished. These are: Group 1, amphibole-bearing shoshonitic lamprophyres (0.5–1.0 wt% Ti0₂, Zr < 150 ppm, Nb < 13 ppm, Ba/Rb < 10); Group 2, mica-bearing shoshonitic lamprophyres (1–1.5 wt% TiO₂, Zr 180 ppm, Nb < 17 ppm, Ba/Rb > 20); Group 3, alkaline lamprophyres (1.5–2.1 wt% TiO₂, Zr > 250 ppm, Nb > 30 ppm, Ba/Rb 10–25); Group 4, low-MgO alkaline lamprophyres ( 2.5 wt% TiO₂, mg-number < 57, Nb 20 ppm, Ba/Rb 20); Group 5, calc-alkaline basaltic dykes ( 2.2 wt% TiO₂, mg-number <55, Nb < 10 ppm, Ba/Rb < 10). Group 2,3 and 4 dykes have NE-SW orientations and are of Oligocene age (K-Ar age 27–32 Ma); Group 1 and 5 dykes are of Lower Oligocene age (K-Ar age 36 Ma) but have mostly E-W orientations.The Kreuzeck lamprophyres were generated in post-collisional magmatic events, which were probably linked to extensional tectonics following oblique continent-continent collision between the African and Eurasian Plates during the Eocene. Group 1, 2 and 5 dyke rocks have typical calc-alkaline geochemical signatures indicating that they represent partial melting products of subduction-modified lithosphere. Group 3 and 4 alkaline lamprophyres have geochemical features transitional between calc-alkaline and within-plate alkaline igneous rocks (e.g. Ba/Nb 30–70) indicating that their mantle source-region includes both subduction-modified lithospheric and OIB-type asthenospheric components.There is no apparent relationship between mineralization in the Kreuzeck region, thought to be of Ordovician-Devonian age, and much later lamprophyre intrusion. Alteration of the dykes by late-magmatic fluids has resulted in the formation of secondary minerals, and has occasionally led to increased Au and PGE values in the 10–35 ppb range particularly in close proximity to Cu-Ag-Au deposits.

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Shoshonitische und alkalische Lamprophyre mit erhöhten Au- und PGE-Gehalten aus der Kreuzeckgruppe, Ostalpen, Österreich

Zusammenfassung Die vorliegende Arbeit untersucht die Petrographie und Geochemie tertiärer Lamprophyre und genetisch verwandter Ganggesteine aus der zentralalpinen Kreuzeckgruppe, nördlich des Periadriatischen Lineamentes, in Kärnten, Österreich. Die Ganggesteine durchschlagen die altpaläozoischen Metapelite, Grünsteine und Amphibolite des Altkristallins diskordant und stehen in räumlichem Zusammenhang mit Sb, W, Hg und Cu-Ag-Au Lagerstätten, die bereits seit dem Mittelalter abgebaut wurden.Die meisten Lamprophyre zeigen primitiven Charakter (Mg-Zahlen >60 und Cr > 200 ppm) und besitzen hohe Gehalte an LILE (K, Rb, Sr und Ba). Geochemisch lassen sich fünf verschiedeneGruppen mit kalkalkalisch/shoshonitischem bis alkalischem Charakter unterscheiden: Gruppe 1, Amphibol-führende shoshonitische Lamprophyre (0.5–1.0 Gew% TiO₂, Zr < 150 ppm, Nb < 13 ppm, Ba/Rb < 10);Gruppe 2, Glimmer-führende shoshonitische Lamprophyre (1–1.5 Gew% TiO₂, Zr 180 ppm, Nb < 17 ppm, Ba/Rb > 20); Gruppe 3, alkalische Lamprophyre (1.5–2.1 Gew% TiO₂, Zr > 250 ppm, Nb > 30ppm, Ba/Rb 10–25); Gruppe 4, alkalische Lamprophyre mit geringen MgO-Anteil ( 2.5 Gew% TiO₂, Mg-Zahl < 57, Nb 20 ppm, Ba/Rb 20); Gruppe 5, kalkalkalisch basaltische Ganggesteine ( 2.2 Gew% TiO₂, Mg-Zahl < 55, Nb < 10 ppm, Ba/Rb < 10). Die Lamprophyre der Gruppen 2, 3 und 4 zeigen nordöstliches Streichen und oligozänes Intrusionsalter (K-Ar Alter 27–32 Ma), während die Ganggesteine der Gruppen 1 und 5 überwiegend östliches Streichen und UnterOligozänes Intrusionsalter (K-Ar Alter 36 Ma) aufweisen.Die Intrusionen erfolgten während einer tektonischen Dilatationsphaseim Oligozän nach der Kontinent-Kontinent Kollision zwischen derAfrikanischen und der Eurasischen Platte im unteren Eozän. Ganggesteine der Gruppen 1, 2 und 5 besitzen typisch kalkalkalischen Charakter und stellen vermutlich Produktevon aufgeschmolzener, subduzierter Lithosphäre dar. Die Geochemie der alkalischen Lamprophyre derGruppen 3 und 4 (e.g. Ba/Nb 30–70) deutet auf ihre genetische Zwischenstellung zwischen subduction-related und within-plate regime.Zwischen den tertiären Gangintrusionen und den vermutlich paläozoischen Vererzungen der Kreuzeckgruppe besteht kein genetischer Zusammenhang. Die Alteration der Ganggesteine durch postmagmatische Lösungen hat jedoch zur Bildung von sekundären Mineralen und teilweise zu überdurchschnittlich erhöhten Au und PGE Gehalten von bis zu 35 ppb geführt.

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With 6 Figures     

A comparative evaluation of minerals and trace elements in the ashes from lignite, coal refuse, and biomass fired power plants

Coal being a limited source of energy, extraction of energy from other sources like lignite, coal-refuse, and biomass is being attempted worldwide. The minerals and inorganic elements present in fuel feeds pose different technological and environmental concerns. Lignite ash, refuse ash, and biomass ash collected from Indian power plants burning lignite, coal-refuse, and mustard stalk, respectively, were analyzed for physico-chemical characteristics and trace elements. The lignite ash has high SiO₂, CaO, MgO, Al₂O_3, and SO₃; the refuse ash has high SiO₂ and Fe₂O₃, but low SO₃; the biomass ash has high SiO₂ (but low Al₂O₃), and high CaO, MgO, K₂O, Na₂O, SO₃, and P₂O₅. A substantial presence of chloride (2.1%) was observed in the biomass ash. Quartz is the most abundant mineral species. Other minerals are mullite, hematite, gehlenite, anhydrite, and calcite in the lignite ash; orthoclase in the refuse ash; albite, sanidine, gehlenite, anhydrite, and calcite in the biomass ash. Ashes with high concentrations (> 100 mg/kg) of trace elements are: lignite ash (V < La < Mn < Cr < Ni < Nd < Ba < Ce, Zn < Sr); refuse ash (Cr < Ce < V < Rb < Mn < Sr, Zn < Ba); biomass ash (Cu < Zn < Ba, Sr). Based on Earth crust normalization, Co, Ni, As, Se, Mo, Zn, Pb, U, and REEs (except Pr and Er) are enriched in the lignite ash; molybdenum, Zn, Cs, Pb, Th, U, La, Ce, and Lu in the refuse ash; and Mo, Zn, Sr, Cs, Pb, and Lu in the biomass ash. Elements As, Zn, Mo, Ni, Pb, Rb, Cr, V, Ba, Sr, and REEs are correlated with Al, indicating the possibilities of their association with aluminum silicates minerals. Similarly, barium, Cs, Th, and U are correlated with iron oxides; molybdenum and Sr may also be associated with sulfates and chlorides. Due to the alkaline nature of these ashes, the high concentrations of As and Se in the lignite ash; molybdenum in the biomass ash; and Se in the refuse ash may pose environmental concerns.     

Geochemistry of eocene calc-alkaline volcanic rocks from the Kastamonu area,Northern Turkey

Analytical data for Sr, Rb, Cs, Ba, Pb, rare earth elements, Y, Th, U, Zr, Hf, Sn, Nb, Mo, Ni, Co, V, Cr, Sc, Cu and major elements are reported for eocene volcanic rocks cropping out in the Kastamonu area, Pontic chain of Northern Turkey. SiO₂% versus K₂O% relationship shows that the analyzed samples belong to two major groups: the basaltic andesitic and the andesitic ones. High-K basaltic andesites and low-K andesites occur too. Although emplaced on continental type basement (the North Anatolian Crystalline Swell), the Pontic eocene volcanics show elemental abundances closely comparable with typical island arc calc-alkaline suites, e.g. low SiO₂% range, low to moderate K₂O% and large cations (Cs, Rb, Sr, Ba, Pb) contents and REE patterns with fractionated light and almost flat heavy REE patterns. REE and highly charged cations (Th, U, Hf, Sn, Zr) are slightly higher than typical calc-alkaline values. Ferromagnesian elements show variable values. Within the basaltic andesite group the increase of K%, large cations, REE, La/Yb ratio and high valency cations and the decrease of ferromagnesian element abundances with increasing SiO₂% content indicate that the rock types making up this group developed by crystalliquid fractionation of olivine and clinopyroxene from a basic parent magma. Trace element concentration suggest that the andesite group was not derived by crystal-liquid fractionation processes from the basaltic andesites, but could represent a distinct group of rocks derived from a different parent magma.     

Crustal contributions to arc magmatism in the Andes of Central Chile

Fifteen andesite-dacite stratovolcanoes on the volcanic front of a single segment of the Andean arc show along-arc changes in isotopic and elemental ratios that demonstrate large crustal contributions to magma genesis. All 15 centers lie 90 km above the Benioff zone and 280±20 km from the trench axis. Rate and geometry of subduction and composition and age of subducted sediments and seafloor are nearly constant along the segment. Nonetheless, from S to N along the volcanic front (at 57.5% SiO₂) K₂O rises from 1.1 to 2.4 wt %, Ba from 300 to 600 ppm, and Ce from 25 to 50 ppm, whereas FeO^*/MgO declines from >2.5 to 1.4. Ce/Yb and Hf/Lu triple northward, in part reflecting suppression of HREE enrichment by deep-crustal garnet. Rb, Cs, Th, and U contents all rise markedly from S to N, but Rb/Cs values double northward — opposite to prediction were the regional alkali enrichment controlled by sediment subduction. K/Rb drops steeply and scatters greatly within many (biotite-free) andesitic suites. Wide diversity in Zr/Hf, Zr/Rb, Ba/Ta, and Ba/La within and among neighboring suites (which lack zircon and alkali feldspar) largely reflects local variability of intracrustal (not slab or mantle) contributions. Pb-isotope data define a limited range that straddles the Stacey-Kramers line, is bracketed by values of local basement rocks, in part plots above the field of Nazca plate sediment, and shows no indication of a steep (mantle+sedimentary) Pb mixing trend. ⁸⁷Sr/⁸⁶Sr values rise northward from 0.7036 to 0.7057, and ¹⁴³Nd/¹⁴⁴Nd values drop from 0.5129 to 0.5125. A northward climb in basal elevation of volcanic-front edifices from 1350 m to 4500 m elevation coincides with a Bougueranomaly gradient from –95 to –295 mgal, interpreted to indicate thickening of the crust from 30–35 km to 50–60 km. Complementary to the thickening crust, the mantle wedge beneath the front thins northward from about 60 km to 30–40 km (as slab depth is constant). The thick northern crust contains an abundance of Paleozoic and Triassic rocks, whereas the proportion of younger arc-intrusive basement increases southward. Primitive basalts are unknown anywhere along the arc. Base-level isotopic and chemical values for each volcano are established by blending of subcrustal and deep-crustal magmas in zones of melting, assimilation, storage and homogenization (MASH) at the mantle-crust transition. Scavenging of mid-to upper-crustal silicic-alkalic melts and intracrustal AFC (prominent at the largest center) can subsequently modify ascending magmas, but the base-level geochemical signature at each center reflects the depth of its MASH zone and the age, composition, and proportional contribution of the lowermost crust.     

Analysis of a weathered profile on sulfide mineralization at Mugga Mugga, Western Australia

The mineralogy and geochemistry of the massive pyrite-pyrrhotite mineralization, which contains minor magnetite, sphalerite and galena, the weathered profile and surface gossan at Mugga Mugga in Western Australia have been examined. Reactions between amphibolite wall rocks and acid waters from the oxidation of the iron sulfides have resulted in distinct mineralogical zonation of the weathered profile which is further modified near the surface by lateritization. At the base of the weathered zone an opaline chert (Opal-CT) has been precipitated from fluctuations of the water table. A gossanous zone from 25.14–68.80 m with boxworks after massive pyrite is modified by abundant kaolinite, dickite and an alunite-type mineral derived from amphibolite wall rocks, while above 25.14 m both plinthite and mottled clay zones of a laterite profile are evident. Some characteristics of a mature gossan profile – sulfate-phosphate-arsenate near the base, a carbonate zone higher in the profile, and an oxide zone near the surface – overprint the gross zonation.At the interface between sulfide and weathered rock Mg, Ca, K, S, Zn, Cd, Hg, Ba are depleted, As, Sb, Mo, Cr and V contents increase and in the weathered zone, SiO₂, TiO₂, P₂O₅, SO₃, Pb, Zn, Hg, Sb, Co, Ni, W, Ba, Sr and Zr decrease up the profile whilst Al₂O₃, Fe₂O₃, CO₂, Cu and As increase. Of the elements associated with the massive pyrite (Pb, Zn, Cu, Ag, As, Cd, Hg, Sb, Co, Ni) anomalous concentrations of Pb, Cu, Ag, As and Sb occur in the surface gossan despite the possibility of complete leaching by highly acidic solutions. These anomalies are similar to those found in gossans over pyrite mineralization elsewhere in the Yilgarn Block.     

Petrology of Karoo volcanic rocks in the southern Lebombo monocline, Mozambique

The Karoo volcanic sequence in the southern Lebombo monocline in Mozambique contains different silicic units in the form of pyroclastic rocks, and two different basalt types. The silicic units in the lower part of the Lebombo sequence are formed by a lower unit of dacites and rhyolites (67–80 wt.% SiO₂) with high Ba (990–2500 ppm), Zr (800–1100 ppm) and Y (130–240 ppm), which are part of the Jozini–Mbuluzi Formation, followed by a second unit, interlayered with the Movene basalts, of high-SiO₂ rhyolites (76–78 wt.%; the Sica Beds Formation), with low Sr (19–54 ppm), Zr (340–480 ppm) and Ba (330–850 ppm) plus rare quartz-trachytes (64–66 wt.% SiO₂), with high Nb and Rb contents (240–250 and 370–381 ppm, respectively), and relatively low Zr (450–460 ppm). The mafic rocks found at the top of the sequence are basalts and ferrobasalts belonging to the Movene Formation. The basalts have roughly flat mantle-normalized incompatible element patterns, with abundances of the most incompatible elements not higher than 25 times primitive mantle. The ferrobasalt has TiO₂  4.7 wt.%, Fe₂O_3t = 16 wt.%, and high Y (100 ppm), Zr (420 ppm) and Ba (1000 ppm). The Movene basalts have initial (at 180 Ma) ⁸⁷Sr/⁸⁶Sr = 0.7052–0.7054 and ¹⁴³Nd/¹⁴⁴Nd = 0.51232, and the Movene ferrobasalt has even lower ⁸⁷Sr/⁸⁶Sr (0.70377) and higher ¹⁴³Nd/¹⁴⁴Nd (0.51259). The silicic rocks show a modest range of initial Sr-(⁸⁷Sr/⁸⁶Sr = 0.70470–0.70648) and Nd-(¹⁴³Nd/¹⁴⁴Nd = 0.51223–0.51243) isotope ratios. The less evolved dacites could have been formed after crystal fractionation of oxide-rich gabbroic cumulates from mafic parental magmas, whereas the most silica-rich rhyolites could have been formed after fractional crystallization of feldspars, pyroxenes, oxides, zircon and apatite from a parental dacite magma. The composition of the Movene basalts imply different feeding systems from those of the underlying Sabie River basalts.