REE and Sr isotope characteristics of carbonate within the Cu–Co mineralized sedimentary sequence of the Nchanga Mine,Zambian Copperbelt

Carbonate, largely in the form of dolomite, is found throughout the host rocks and ores of the Nchanga mine of the Zambian Copperbelt. Dolomite samples from the hanging wall of the mineralization show low concentrations of rare-earth elements (REE) and roof-shaped, upward convex, shale-normalized REE patterns, with positive Eu*_SN anomalies (1.54 and 1.39) and marginally negative Ce anomalies (Ce*_SN 0.98,0.93). In contrast, dolomite samples associated with copper and cobalt mineralization show a significant rotation of the REE profile, with HREE enrichment, and La/Lu_SN ratios <1 (0.06–0.42). These samples also tend to show variable but predominantly negative Eu*_SN and positive cerium anomalies and an upwardly concave MREE distribution (Gd-Er). Malachite samples from the Lower Orebody show roof-tile-normalized REE patterns with negative europium anomalies (Eu*_SN 0.65–0.80) and negative cerium anomalies (Ce*_SN 0.86–0.9). The carbonate ⁸⁷Sr/⁸⁶Sr signature correlates with the associated REE values. The uppermost dolomite samples show Neoproterozoic seawater-like ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7111 to 0.7116, whereas carbonate from Cu–Co mineralized samples show relatively low concentrations of strontium and more radiogenic ⁸⁷Sr/⁸⁶Sr, ranging between 0.7136–0.7469. The malachite samples show low concentrations of strontium, but give a highly radiogenic ⁸⁷Sr/⁸⁶Sr of 0.7735, the most radiogenic ⁸⁷Sr/⁸⁶Sr ratio. These new data suggest that the origin and timing of carbonate precipitation at Nchanga is reflected in the REE and Sr isotope chemistry. The upper dolomite samples show a modified, but essentially seawater-like signature, whereas the rotation of the REE profile, the MREE enrichment, the development of a negative Eu*_SN anomaly and more radiogenic ⁸⁷Sr/⁸⁶Sr suggests the dolomite in the Cu–Co mineralized samples precipitated from basinal brines which had undergone significant fluid–rock interaction. Petrographic, REE, and ⁸⁷Sr/⁸⁶Sr data for malachite are consistent with the original sulfide Lower Orebody being subject to a later oxidizing event.     

REE Geochemical Characteristics of Volcanic Rocks in Zhejiang and Jiangxi Provinces and Their Gological Significance

Based on the data of 64 samples ,the REE geochemical characteristics of volcanic rocks in northern Zhejiang and eastern Jiangxi provinces are discussed in this paper.The REE distribution patterns in acid and intermediate-acid volcanic rocks in these areas display some similarities,as indicated by rightward-inclined V-shaped curves with negative Eu anomalies,which are parallel to earch other.In addi-tion,their REE parameters(ΣREE,ΣLREE/ΣHREE,δEu,Ce/Yb,La/Sm,La/Yb,etc)also va-ry over a narrow range with small deviations.HREE are particularly concentrated in the volcanic rocks as-sociated with uranium mineralization.The initial ^87Sr/^86Sr ratio in the volcanic rocks is about 0.7056-0.7139.All these features in conjunction with strontium isotopic data indicate that the rock-forming materials come from the sialic crust.The REE distribution patterns and REE geochemical parameters of the volcanic rocks ,as well as La/Sm-La and Ce/Yb-Eu/Yb diagrams may be applied to the sources of rock-forming and ore-forming materials.     

Geochemical characteristics of Cenozoic high-K igneous rocks from Liuhe-Xiangduo area, eastern Tibet

The major elements, trace elements and Nd-Sr isotopic composition of Cenozoic high-K igneous rocks and mafic deep-derived enclaves from the Liuhe-Xiangduo area, eastern Tibet, indicate the high-K igneous rocks are characterized as being enriched in Ca (CaO= 1.20% - 8.80% ), alkali (Na2O K2O= 3.47% - 10.65% ), especially K (K2O up to 5.96% ) and depleted in Ti (TiO2= 0.27% - 1.50% ). Their REE contents are very high (REE= 91.29 - 231.11 μg/g). Their REE distribution patterns are of the right-inclined type, characterized by intense LREE enrichment [(La/Yb)N= 7.44 - 15.73 ]. The rocks are distinctly enriched in Rb, Sr and Ba ( 46.3 -316 μg/g, 349-1220 μg/g and 386-2394 μg/g, respectively), high in U and Th ( 1.17 - 8.10 μg/g and 2.58 - 27.0 μg/g, respectively), moderate in Zr and Hf ( 87.5 -241 μg/g and 2.83 - 7.52 μg/g, respectively), and depleted in Nb and Ta ( 4.81 - 16.8 μg/g and 0.332 - 1.04 μg/g, respectively). In the primitive mantle-normalized incompatible element spidergram, U, K, Sr and Hf show positive anomalies, whereas Th, Nb, Ta, P, and Ti show negative anomalies. The rocks are strongly depleted in Cr and Ni ( 21.4 -1470 μg/g and 7.79 -562 μg/g, respectively), and their transition element distribution curves are obviously of type-W. The ( 87 Sr/ 86 Sr)i ratios range from 0.704184 to 0.707539 ; ( 143 Nd / 144 Nd)i from 0.512265 to 0.512564 ; and ε Nd (t) from -6.3 to -0.4 . These geochemical features might suggest that the potential source of the high-K igneous rocks in the Liuhe-Xiangduo area is similar to the EM2, which may be similar to the material enriched K that is located under the crust-mantle mixed layer. The mafic deep-derived enclaves in the high-K igneous rocks belong to chance xenoliths. Their ( 87 Sr/ 86 Sr)i ratios range from 0.706314 to 0.707198 ; ( 143 Nd / 144 Nd)i from 0.512947 to 0.513046 ; and ε Nd (t) from 7.0 to 9.0 . These geochemical features might indicate that the enclaves probably came from the depleted mantle. The P-T conditions of the enclaves also showed that the enclaves are middle-lower crust metamorphic rocks, which were accidentally captured at 20-50 km level by rapidly entrained high-K magma, whose source is over 50 km in depth.     

REE Geochemistry of Precambrian Metamorphic Rocks in Wutaishan Region

The metasedimentary-volcanic series of the Wutai and Hutuo groups experienced regional metamorphism and thus turned into moderate-to low-grade metamorphic rocks.REE abundances and REE distribution patterns in the Shizui and Taihuai Subgroup metasedimentary-volcanic rocks are typical of the Archean,whereas the Gaofan Subgroup and the Hutuo Group show post-Archean REE geochemical char-acteristics.Five types of REE distribution pattern are distinguished:(1)rightward inclined smooth curves with little REE anomaly(Eu/Eu*=0.73-0.95) and heavy REE depletion (e.g.the Late Archean metasedimentary rocks);(2)rightward inclined V-shaped curves with sharp Eu anoma-ly (Eu/Eu*=0.48-0.76) and slightly higher ∑REE (e.g.the post-Archean metasedimentary rocks);(3) rightward inclined steep curves with negative Eu anomaly(Eu/Eu*=0.73-0.76) and the lowest ∑REE (e.g.the post-Archean dolomites);(4)rightward inclined,nearly smooth curves with both positive Eu anomaly and unremarkable positive Eu anomaly(Eu/Eu*=0.95-1.25)(e.g.the meta-basic volcanic rocks);and (5) rightward inclined curves with Eu anomaly(Eu/Eu*=1.09-1.19)and heavy REE depletion(e.g.the meta-acid volcanic rocks).Strata of the two groups are considered to have been formed in an island-arc belt-an instable continental petrogenetic environment.     

Nature of the crust in Maine,USA: evidence from the Sebago batholith

 Neodymium and lead isotope and elemental data are presented for the Sebago batholith (293±2 Ma), the largest exposed granite in New England. The batholith is lithologically homogeneous, yet internally heterogeneous with respect to rare earth elements (REE) and Nd isotopic composition. Two-mica granites in the southern/central portion of the batholith (group 1) are characterized by REE patterns with uniform shapes [Ce_N/Yb_N (chondrite normalized) = 9.4–19 and Eu/Eu* (Eu anomaly) = 0.27–0.42] and ɛ _Nd(t) = −3.1 to −2.1. Peripheral two-mica granites (group 2), spatially associated with stromatic and schlieric migmatites, have a wider range of total REE contents and patterns with variable shapes (Ce_N/Yb_N = 6.1–67, Eu/Eu* = 0.20–0.46) and ɛ _Nd(t) = −5.6 to −2.8. The heterogeneous REE character of the group 2 granites records the effects of magmatic differentiation that involved monazite. Coarse-grained leucogranites and aplites have kinked REE patterns and low total REE, but have Nd isotope systematics similar to group 2 granites with ɛ _Nd(t) = −5.5 to −4.7. Rare biotite granites have steep REE patterns (Ce_N/Yb_N = 51–61, Eu/Eu* = 0.32–0.84) and ɛ _Nd(t) = −4.6 to −3.8. The two-mica granites have a restricted range in initial Pb isotopic composition (²⁰⁶Pb/²⁰⁴Pb = 18.41–18.75; ²⁰⁷Pb/²⁰⁴Pb = 15.60–15.68; ²⁰⁸Pb/²⁰⁴Pb = 38.21–38.55), requiring and old, high U/Pb (but not Th/U) source component. The Nd isotope data are consistent with magma derivation from two sources: Avalon-like crust (ɛ _Nd>−3), and Central Maine Belt metasedimentary rocks (ɛ _Nd<−4), without material input from the mantle. The variations in isotope systematics and REE patterns are inconsistent with models of disequilibrium melting which involved monazite. Received: 8 December 1995 / Accepted: 29 April 1996     

Late Mesozoic collisional granitoids of the upper Amur area: New geochemical data

Geochemical and isotopic data were used for a comparative analysis of Late Mesozoic (150–120 Ma) granitoids in various geological structures of the upper Amur area. The granitoids are metaluminous high-potassic I-type rocks of the magnetite series. They have variable alkalinity and consist of the monzonite-granite and granosyenite-granite associations. The monzonite-granite association consists of calc-alkaline granitoids of normal alkalinity belonging to the Umlekan-Ogodzhinskaya volcanic-plutonic zone and the Tynda-Bakaran Complex of the Stanovoy terrane. The rocks are characterized by negative anomalies of U, Ta, Nd, Hf, and Ti (in patterns normalized to the primitive mantle), with Eu anomalies pronounced weakly in the granodiorites and quartz and monzodiorites and more clearly in the granites: Eu/Eu* = 0.37–0.95, and (La/Yb)_n = 7–24, Tb_n/Yb_n = 1.4–3.2. The granosyenite-granite association comprises of moderately alkaline rocks, which are subdivided into three groups according to their geochemistry. The first group consists of phase-I granosyenites of the Uskalinskii Massif of the Umlekan-Ogodzhinskaya zone with the highest concentrations of Sc, V, Cr, Co, Ni, Cu, Cs, Rb, Sr, Y, Zr, Yb, and Th; negative anomalies at Ba, Ta, Sr, and Hf; Eu/Eu* = 0.50–0.58, (La/Yb)_n = 15–16, and Tb_n/Yb_n = 1.8. The second group comprises of moderately alkaline granitoids of the Umlekan-Ogodzhinskaya zone and the Khaiktinskii Complex of the Baikal-Vitim superterrane. Geochemically, the granitoids of this group are generally similar to the monzodiorite-granite association and differ from it in having lower concentrations of REE and Y, Eu/Eu* = 6.2–1.0, (La/Yb)_n = 28–63, and Tb_n/Yb_n = 2.1–4.5. The third group consists of granitoids of the Chubachinskii Complex of the Stanovoi terrane, which typically show negative Cs, Rb, Th, U, Ta, Hf, and Ti anomalies; the lowest concentrations of V, Cr, Co, and Ni; and the highest contents of Sr. The granosyenites of the first phase display clearly pronounced negative Eu anomalies (Eu/Eu* = 0.53–0.68), (La/Yb)_n = 7–24, and Tb_n/Yb_n = 0.8–2.0. The granitoids of the second phase have (La/Yb)_n = 51–84, no Eu anomalies, or very weak Eu anomalies (Eu/Eu* = 0.97–1.23). The silica-oversaturated leucogranites of the third phase are characterized by elevated concentrations of REE, clearly pronounced Eu anomalies (Eu/Eu* = 0.48), and flat REE patterns (Tb_n/Yb_n = 1.3). The diversity of the granitoids is demonstrated to have been caused largely by the composition of the Precambrian source, which was isotopically heterogeneous. The rocks of the monzodiorite-granite association and first-group granosyenites of the granosyenite-granite association of the Tynda-Bakaran Complex were supposedly derived from garnet-bearing biotite amphibolites. In contrast to these rocks, the source of the second-group granites of the granosyenite-granite association was of mixed amphibolite-metagraywacke composition. The third-group of granitoids were melted out of Early Proterozoic crustal feldspar-rich granulites of variable basicity, with minor amounts of Archean crustal material. The granitoids were emplaced in a collisional environment, perhaps, during the collision of the Amur superterrane and Siberian craton. This makes it possible to consider these rocks as components of a single continental volcanic-plutonic belt. Original Russian Text ? V.E. Strikha, 2006, published in Geokhimiya, 2006, No. 8, pp. 855–872.     

Geochemical characteristics of pyrite in Duolanasayi gold deposit, Xinjiang

The Duolanasayi gold deposit, 60 km NW of Habahe County, Xinjiang Uygur Autonomous Region, is a mid-large-scale gold deposit controlled by brittle-ductile shearing, and superimposed by albitite veins and late-stage magma hydrothermal solutions. There are four types of pyrite, which are contained in the light metamorphosed rocks (limestone, siltstone), altered-mineralized rocks (chlorite-schist, altered albite-granite, mineralized phyllite), quartz veins and carbonatite veinlets. The pyrite is the most common ore mineral. The Au-barren pyrite is present mainly in a simple form and gold-bearing pyrite is present mainly in a composite form. From the top downwards, the pyrite varies in crystal form from {100} and {210} {100} to {210} {100} {111} to {100} {111}. Geochemical studies indicate that the molecular contents of pyrite range from Fe1.057S2 to Fe0.941S2. Gold positively correlates with Mn, Sr, Zn, Te, Pb, Ba and Ag. There are four groups of trace elements: Fe-Cu-Sr-Ag, Au-Te-Co, As-Pb-Zn and Mn-V-Ti-Ba-Ni-Cr in pyrite. The REE characteristics show that the total amount of REE (ΣREE) ranges from 32.35×10 -6 to 132.18×10 -6; LREE/HREE, 4.466-9.142; (La/Yb)N, 3.719-11.133; (Eu/Sm)N, 0.553-1.656; (Sm/Nd)N, 0.602-0.717; La/Yb, 6.26-18.75; δEu, 0.628-2.309; δCe, 0.308-0.816. Sulfur isotopic compositions (δ 34S=-2.46‰--7.02‰) suggest that the sulfur associated with gold mineralization was derived from the upper mantle or lower crust.     

Deep-derived enclaves （belonging to middle-lower crust metamorphic rocks） in the Liuhe-Xiangduo area, eastern Tibet： Evidence from petrogeochemistry

1IntroductionMany investigations have been made on the deep-derived enclaves fromCenozoic high-Kigneous rocks inthe Liuhe-Xinagduo area,eastern Tibet,by many re-searchers from different aspects since the90s of the20th century(Cai Xinping,1992;Deng Wanming…     

Magnesian andesites in north Xinjiang,China

Middle Devonian magnesian andesites (MAs) are widely distributed in south Altay and Carboniferous MAs are present in Alataoshan and west- and east-Tianshan in the north Xinjiang region. These MAs are andesitic rocks with 53–65% SiO₂,<1% (0.21–1.08%; average of 0.72%) TiO₂, and ≥50 Mg^#. Magnesian dacites and diorites, with 52.38–66.91% SiO₂, <0.30% TiO₂ and ≥42 Mg^# commonly occur with these MAs. Relative to boninites, MAs have lower MgO contents (average 6.39%) but higher Ti, K and Na. They have characteristic flat chondrite-normalized REE patterns with weak to no Eu anomalies (Eu depletion, or Eu/Eu* = 0.65–1.15), low (La/Yb)_N (0.98–6.4, mostly 4±) and low total REE contents (15–95 ppm). They also have high contents of compatible elements Cr and Ni (72–790 and 29–276 ppm, respectively). Their relative depletion in high field strength elements Nb, Ta and Ti, and relative enrichment in mobile large-ion lithophile elements Rb, K and Pb are evident on primitive mantle-normalized trace element spidergrams. If magnesian andesites are melts coming from the subducted oceanic crust, as proposed elsewhere, then the relatively high Y contents (>15 ppm), low Sr/Y ratios (4.4–6.2), low (La/Yb)N, and high Mg^# of the MAs in north Xinjiang provide evidence of interaction of such melts with mantle wedge peridotite. New petrographic, chemical and isotopic [(¹⁴³Nd/¹⁴⁴Nd)I = 0.51221–0.51255 (εNd(t) +0.28 to +7.2); (⁸⁷Sr/⁸⁶Sr)I = 0.7029–0.7065] data suggest that the petrogenesis of the MAs in the north Xinjiang region may have involved: (1) multiple source materials including subducted oceanic slab, juvenile crustal materials (mainly volcanic-volcanoclassic rocks with low maturity and clear mantle geochemical signatures) coming from the forearc accretionary prism and mantle wedge peridotite; (2) a combination of different petrogenetic processes including partial melting of subducted oceanic slab and juvenile crustal materials, followed by interaction of slab melts with the mantle wedge peridotite; (3) high geothermal gradient creating a high temperature (>1,000°C) environment in a volatile-rich source region; (4) unique tectonic settings including oblique subduction, slab break off resulting in slab window formation and asthenosphere upwelling, and subduction erosion resulting in transfer of forearc accretionary materials into the source region of MA magma.     

Early Cretaceous highly positive <Emphasis Type="Italic">ε</Emphasis><Subscript>Nd</Subscript> felsic volcanic rocks from the Hinggan Mountains,NE China: origin and implications for Phanerozoic crustal growth

An early Cretaceous (135 ± 2 Ma) felsic volcanic suite of dacite and rhyolite from Huolinhe, NE China is characterized by large ion lithophile element and light REE enrichment and high field strength element (HFSE, e.g., Nb and Ta) and Ti–P depletion, and bulk silicate earth-like Sr [⁸⁷Sr/⁸⁶Sr(i) = 0.70409–0.70481], quite radiogenic Nd [ε _Nd(t) = +3.98 to +5.88], Pb [e.g., ²⁰⁶Pb/²⁰⁴Pb(i) = 18.46–18.55] and Hf [ε _Hf(t) ~+9.2] isotope compositions. Compared with contemporaneous mafic rocks in the region, these felsic rocks have even higher Nd and Hf isotopic ratios, precluding an origin through differentiation of coeval mantle-derived magmas. Isotope calculation results suggest that these magmas were derived from a preexistent mixture composed of mainly juvenile crust (70–80%), and a subordinate recycled crustal component (20–30%) having highly radiogenic Sr and Pb and unradiogenic Nd and Hf. About 25–30% melting of such a mixed source produced the primary dacitic magma. The rhyolites, which have relatively low MgO, FeO*, Al₂O₃, CaO, TiO₂, P₂O₅, Na₂O, Ba, Sr, REE, HFSE and Y, were differentiates of the dacites after removal of a fractional assemblage of hornblende + plagioclase + K-feldspar + apatite + zircon. Considering the prolonged events (from 262 to 130 Ma) that produced such highly positive ε _Nd felsic igneous rocks in the region, we prefer a pre-Mesozoic crustal growth model related to arc accretion associated with the Paleo-Asian Ocean subduction.     

The petrogenesis of volcanics from Mt. Bulusan and Mt. Mayon in the Bicol arc,the Philippines

Pliocene to recent volcanic rocks from the Bulusan volcanic complex in the southern part of the Bicol arc (Philippines) exhibit a wide compositional range (medium- to high-K basaltic-andesites, andesites and a dacite/rhyolite suite), but are characterised by large ion lithophile element enrichments and HFS element depletions typical of subduction-related rocks. Field, petrographic and geochemical data indicate that the more silicic syn- and post-caldera magmas have been influenced by intracrustal processes such as magma mixing and fractional crystallisation. However, the available data indicate that the Bicol rocks as a group exhibit relatively lower and less variable ⁸⁷Sr/⁸⁶Sr ratios (0.7036–0.7039) compared with many of the other subduction-related volcanics from the Philippine archipelago. The Pb isotope ratios of the Bicol volcanics appear to be unlike those of other Philippine arc segments. They typically plot within and below the data field for the Philippine Sea Basin on ²⁰⁷Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb diagrams, implying a pre-subduction mantle wedge similar to that sampled by the Palau Kyushu Ridge, east of the Philippine Trench. ¹⁴³Nd/¹⁴⁴Nd ratios are moderately variable (0.51285–0.51300). Low silica (<55 wt%) samples that have lower ¹⁴³Nd/¹⁴⁴Nd tend to have high Th/Nd, high Th/Nb, and moderately low Ce/Ce* ratios. Unlike some other arc segments in the Philippines (e.g. the Babuyan-Taiwan segment), there is little evidence for the involvement of subducted terrigenous sediment. Instead, the moderately low ¹⁴³Nd/¹⁴⁴Nd ratios in some of the Bicol volcanics may result from subduction of pelagic sediment (low Ce/Ce*, high Th/Nd, and high Th/Nb) and its incorporation into the mantle wedge via a slab-derived partial melt.     

Stable isotope and Rare Earth Element evidence for recent ironstone pods within the Archean Barberton greenstone belt, South Africa

There is considerable debate about the mode and age of formation of large (up to ∼200 m long) hematite and goethite ironstone bodies within the 3.2 to 3.5 Ga Barberton greenstone belt. We examined oxygen and hydrogen isotopes and Rare Earth Element (REE) concentrations of goethite and hematite components of the ironstones to determine whether these deposits reflect formation from sea-floor vents in the Archean ocean or from recent surface and shallow subsurface spring systems. Goethite δ¹⁸O values range from −0.7 to +1.0‰ and δD from −125 to −146‰, which is consistent with formation from modern meteoric waters at 20 to 25 °C. Hematite δ¹⁸O values range from −0.7 to −2.0‰, which is consistent with formation at low to moderate temperatures (40-55 °C) from modern meteoric water. REE in the goethite and hematite are derived from the weathering of local sideritic ironstones, silicified ultramafic rocks, sideritic black cherts, and local felsic volcanic rocks, falling along a mixing line between the Eu/Eu* and shale-normalized HREE_Avg/LREE_Avg values for the associated silicified ultramafic rocks and felsic volcanic rocks. Contrasting positive Ce/Ce* of 1.3 to 3.5 in hematite and negative Ce/Ce* of 0.2 to 0.9 in goethite provides evidence of oxidative scavenging of Ce on hematite surfaces during mineral precipitation. These isotopic and REE data, taken together, suggest that hematite and goethite ironstone pods formed from relatively recent meteoric waters in shallow springs and/or subsurface warm springs.     

The adakite connection of the Tuwu–Yandong copper porphyry belt, eastern Tianshan, NW China: trace element and Sr-Nd-Pb isotope geochemistry

The Tuwu–Yandong porphyry copper belt lies in the eastern Tianshan mountains, eastern section of the Central Asian orogenic belt. The copper mineralization is mainly hosted in plagiogranite porphyries intruded into early Carboniferous volcanic rocks of the Paleozoic Dananhu island arc between the Tarim and Siberian plates. The plagiogranite porphyries have contents of 65–73 wt% SiO₂, 14–17 wt% Al₂O₃, 0.9–2.2 wt% MgO, 3–16 ppm Y, 0.4–1.40 ppm Yb, 347–920 ppm Sr, and positive Eu anomalies. The rocks also exhibit positive ɛ _Nd(t) values (+5.0 to +9.4) and low initial ⁸⁷Sr/⁸⁶Sr values (0.70316–0.70378). Such features are similar to those of adakites derived from partial melting of a subduction-related oceanic slab. The mineralization age is early Carboniferous (350–320 Ma), which is close to that of the porphyries. The close relationship between the Cu mineralization and the porphyry is also indicated by their similar Sr-Nd-Pb isotopic compositions. We suggest that the copper porphyry (magma) system in the Dananhu island arc was formed by direct melting of an obliquely subducting early Carboniferous oceanic slab.     

Geochemistry and petrogenesis of granitoids of Lesser Himalayan crystallines,Western Arunachal Himalaya

Low to medium grade crystalline rocks locally known as Bomdila Group extensively covers the Lesser Himalayan region in Western Arunachal Himalaya. This Group consists dominantly of mylonitic gneisses of granitic composition of Palaeoproterozoic age, named as Bomdila mylonitic gneiss (BMG) and a small body of hornblende bearing granite of Mesoproterozoic age known as Salari granite (SG). The BMG is affinity to peraluminous (A/CNK > 1.1) with high content of SiO₂, K₂O/Na₂O ratio, normative corundum, high ratio of FeO^t/MgO in biotite (3.21–5.11) that shows characteristics of S-type granite whereas SG has granodiorite composition with high Na₂O, low K₂O, presence of hornblende, normative diopside, low A/CNK ratio (<1.1) and low FeO^t/MgO ratio in biotite (1.58–1.60) indicates metaluminous I-type granite affinity. The SG has more fractionated nature of REE [(Ce/Yb)_N = 9.06–18.53] and minor negative Eu anomalies [Eu_N/Eu* = 0.69–0.94] as compared to BMG which has less fractionation of REE [(Ce/Yb)_N = 5.95–9.16] and strong negative Eu anomalies [Eu_N/Eu* = 0.37–0.43]. Geochemical and petrological studies suggest that the SG and BMG are not genetically related; SG appears to have derived from igneous source whereas the BMG have been derived from sedimentary source, however these granitoids might have produced during the same thermal event.     

The Ashele VMS-type Cu-Zn Deposit in Xinjiang,NW China Formed in a Rifted Arc Setting

The Ashele Cu-Zn deposit is a typical VMS deposit in Chinese Altay located in the southern margin of the Altaid orogen. The deposit occurred in the polyphase fold system, and the main orebody is located at the hinge of the syncline. All orebodies show lenticular form, and are stratabound by a suite of early to middle Devonian bimodal volcanic rocks. The hosting basalt is low K tholeiite and characterized with high Mg, Fe, Ca and low K, Ti. These basalts show flat REE pattern with Ce negative anomaly (Ce/Ce* 0.73–0.76). Niobium, Ta, Zr, Hf are depleted and Rb, Ba, Th, U, Sr, Pb are enriched with respect to the N-MORB. Both the Sr and Nd isotopes show depleted properties, while the (⁸⁷Sr/⁸⁶Sr)_i and the ε_Nd(t) range from 0.70469 to 0.70488 and 4.6 to 5.3, respectively. All geochemical and isotopic data from the hosting basalt show that it originates from an island arc source. We also report the S isotope data from the massive orebody, and δ³⁴S‰ change from 1.8‰ to 5.6‰. The S isotope data provide evidence that the sulfur originates from a mixing source between magma and seawater sulfate. We propose that the mafic magma provides the ore-forming metal and some percentage of sulfur, while it also acts as a heat engine which makes the fluids leach the metal from the underlying volcanic rocks. Combining the geological characteristics of the Ashele and geochemical data, and comparing with other Cu-Zn VMS deposits in the world, we propose that Ashele formed in a rifted arc setting.     

Adakite-like volcanism of Ecuador: lower crust magmatic evolution and recycling

In the Northern Andes of Ecuador, a broad Quaternary volcanic arc with significant across-arc geochemical changes sits upon continental crust consisting of accreted oceanic and continental terranes. Quaternary volcanic centers occur, from west to east, along the Western Cordillera (frontal arc), in the Inter-Andean Depression and along the Eastern Cordillera (main arc), and in the Sub-Andean Zone (back-arc). The adakite-like signatures of the frontal and main arc volcanoes have been interpreted either as the result of slab melting plus subsequent slab melt–mantle interactions or of lower crustal melting, fractional crystallization, and assimilation processes. In this paper, we present petrographic, geochemical, and isotopic (Sr, Nd, Pb) data on dominantly andesitic to dacitic volcanic rocks as well as crustal xenolith and cumulate samples from five volcanic centers (Pululagua, Pichincha, Ilalo, Chacana, Sumaco) forming a NW–SE transect at about 0° latitude and encompassing the frontal (Pululagua, Pichincha), main (Ilalo, Chacana), and back-arc (Sumaco) chains. All rocks display typical subduction-related geochemical signatures, such as Nb and Ta negative anomalies and LILE enrichment. They show a relative depletion of fluid-mobile elements and a general increase in incompatible elements from the front to the back-arc suggesting derivation from progressively lower degrees of partial melting of the mantle wedge induced by decreasing amounts of fluids released from the slab. We observe widespread petrographic evidence of interaction of primary melts with mafic xenoliths as well as with clinopyroxene- and/or amphibole-bearing cumulates and of magma mixing at all frontal and main arc volcanic centers. Within each volcanic center, rocks display correlations between evolution indices and radiogenic isotopes, although absolute variations of radiogenic isotopes are small and their values are overall rather primitive (e.g., ε_Nd = +1.5 to +6, ⁸⁷Sr/⁸⁶Sr = 0.7040–0.70435). Rare earth element patterns are characterized by variably fractionated light to heavy REE (La/Yb_N = 5.7–34) and by the absence of Eu negative anomalies suggesting evolution of these rocks with limited plagioclase fractionation. We interpret the petrographic, geochemical, and isotopic data as indicating open-system evolution at all volcanic centers characterized by fractional crystallization and magma mixing processes at different lower- to mid-crustal levels as well as by assimilation of mafic lower crust and/or its partial melts. Thus, we propose that the adakite-like signatures of Ecuadorian rocks (e.g., high Sr/Y and La/Yb values) are primarily the result of lower- to mid-crustal processing of mantle-derived melts, rather than of slab melts and slab melt–mantle interactions. The isotopic signatures of the least evolved adakite-like rocks of the active and recent volcanoes are the same as those of Tertiary ”normal” calc-alkaline magmatic rocks of Ecuador suggesting that the source of the magma did not change through time. What changed was the depth of magmatic evolution, probably as a consequence of increased compression induced by the stronger coupling between the subducting and overriding plates associated with subduction of the aseismic Carnegie Ridge.     

Dokhan volcanics of Gabal Monqul area,North Eastern Desert,Egypt: geochemistry and petrogenesis

The Dokhan volcanics are represented by a thick stratified lava flows succession of basalt, andesite, imperial porphyry, dacite, rhyodacite, rhyolite, ignimbrites, and tuffs. These lavas are interbanded with their pyroclastics in some places including banded ash flow tuffs, lithic tuffs, crystal lapilli tuffs, and agglomerates. They are typical calc–alkaline and developed within volcanic arc environment. All rocks show moderate enrichment of most large ion lithophile elements relative to high field strength elements (HFSE). The incompatible trace elements increase from basalt through andesite to rhyolite. The felsic volcanics are characterized by moderate total rare earth elements (REE) contents (162 to 392 ppm), less fractionated patterns {(Ce/Yb)_N = (1.24 to 10.93)}, and large negative Eu anomaly {(Eu/Eu*) = (0.15 to 0.92)}. The mafic volcanics have the lowest REE contents (61 to 192 ppm) and are relatively steep {(Ce/Yb)_N = (3.2 to 8.5)}, with no negative Eu anomalies {(Eu/Eu*) = (0.88 to 1)}. The rhyolite displays larger negative Eu anomaly (Eu/Eu* = 0.28) than those of other varieties, indicating that the plagioclase was an early major fractionating phase. The mineralogical and chemical variations within volcanics are consistent with their evolution by fractional crystallization of plagioclase and clinopyroxene.     

Sr,Nd and Pb isotopic and geochemical constraints for the origin of magmas in Popocatépetl volcano (central Mexico) and their relationship with the adjacent volcanic fields

We present new geochemical data (major- and trace-elements, as well as Sr and Nd isotopic compositions) of volcanic rocks erupted from Popocatépetl volcano during the volcanic event from December 2000 to January 2001. These data along with an exhaustive compilation of geochemical and Sr, Nd, and Pb isotope data reported for Popocatépetl rocks and nearby volcanic areas are used to examine the origin and geochemical evolution of the magmas in the central Mexican volcanic belt (CMVB). During this period of volcanic eruptions Popocatépetl produced ash columns as high as 7 km. Pyroclastic flows and lahars were observed after the completion of the activity. Samples of banded pumice and a bomb fragment transported by the lahar were chemically analysed for this work. Rocks show an andesitic composition with 58.5–61.7 wt.% SiO₂ and 5.9–4.0 wt.% MgO. Contents of large ion lithophile elements (LILE), rare-earth elements (REE) and Zr are nearly constant through the compositional range. No significant Eu anomaly is present, but the samples show Nb-anomaly relative to LILE and high-field strength elements (HFSE). Nd- and Sr-isotopic compositions of these samples range from ¹⁴³Nd/¹⁴⁴Nd = 0.51291 to 0.51287 and ⁸⁷Sr/⁸⁶Sr = 0.70399 to 0.70422. Comparison of Popocatépetl products with volcanic rocks from the nearby areas shows that the magmas in CMVB were generated in a heterogeneously veined-mantle source enriched in LILE, HFSE, and REE. Additional crustal assimilation as well as fractional crystallization could account for the great chemical variability of rocks in the CMVB. Statistical comparison of the geochemical compositions of the volcanic products ejected from 1994 to 2000 to those ejected during the 2001 event shows that most geochemical parameters (major- and trace-elements, normative minerals, Sr and Nd isotopic composition, as well some elemental ratios) present no statistically significant differences. Statistically significant differences in the mean only were computed for the major-elements SiO₂, FeO, MgO, CaO, and K₂O, as well as for the rare-earth elements Nd, Sm, Eu, Gd, Dy, Ho, Tm, and Yb.     

Permian volcanic rocks from the Apuseni Mountains (Romania): Geochemistry and tectonic constraints

An Early Permian volcanic assemblage is well exposed in the central-western part of the Apuseni Mountains (Romania). The rocks are represented by rhyolites, basalts and subordinate andesites suggesting a bimodal volcanic activity that is intimately associated with a post-orogenic (Variscan) syn-sedimentary intra-basinal continental molasse sequences. The mafic and mafic-intermediate rocks belong to sub-alkaline tholeiitic series were separated in three groups (I–III) showing a high Th and Pb abundances, depletion in Nb, Ta and Sr, and slightly enriched in LREE patterns (La_N/Yb_N = 1.4–4.4). Isotopically, the rocks of Group I have the initial ratios ⁸⁷Sr/⁸⁶Sr_(i) = 0.709351–0.707112, ¹⁴³Nd/¹⁴⁴Nd_(i) = 0.512490–0.512588 and high positive ?_Nd270 values from 3.9 to 5.80; the rocks of Group II present for the initial ratios values ⁸⁷Sr/⁸⁶Sr_(i) = 0.709434–0.710092, ¹⁴³Nd/¹⁴⁴Nd_(i) = 0.512231–0.512210 and for ?_Nd270 the negative values from −1.17 to −1.56; the rocks of Group III display for the initial ratios the values ⁸⁷Sr/⁸⁶Sr_(i) = 0.710751–0.709448, ¹⁴³Nd/¹⁴⁴Nd_(i) = 0.512347–0.512411 and for ?_Nd270 the positive values from 1.64 to 2.35. The rocks resembling continental tholeiites, suggest a mantle origin and were further affected by fractionation and crustal contamination. In addition, the REE geochemistry (1 > Sm_N/Yb_N < 2.5; 0.9 > La_N/Sm_N < 2.5) suggests that these rocks were generated by high percentage partial melting of a metasomatized mantle in the garnet peridotite facies. The felsic rocks are enriched in Cs, Rb Th and U and depleted in Nb, Ta, Sr, Eu, and Ti. The REE fractionation patterns show a strong negative Eu anomaly (Eu/Eu* = 0.23–0.40). The felsic rocks show the initial ratios the values: ⁸⁷Sr/⁸⁶Sr_(i) = 0.704096–0.707805, ¹⁴³Nd/¹⁴⁴Nd_(i) = 0.512012–0.512021 and for ?_Nd270 the negative values from −5.27 to −5.44. They suggest to be generated within the lower crust during the emplacement of mantle-derived magmas that provided necessary heat to crustal partial melting.     

An overview on geochemistry of Proterozoic massif-type anorthosites and associated rocks

A critical study of 311 published WR chemical analyses, isotopic and mineral chemistry of anorthosites and associated rocks from eight Proterozoic massif anorthosite complexes of India, North America and Norway indicates marked similarities in mineralogy and chemistry among similar rock types. The anorthosite and mafic-leucomafic rocks (e.g., leuconorite, leucogabbro, leucotroctolite, anorthositic gabbro, gabbroic anorthosite, etc.) constituting the major part of the massifs are characterized by higher Na₂O + K₂O, Al₂O₃, SiO₂, Mg# and Sr contents, low in plagioclase incompatible elements and REE with positive Eu anomalies. Their δ ¹⁸O‰ (5.7–7.5), initial ⁸⁷Sr/⁸⁶Sr (0.7034–0.7066) and ɛ _Nd values (+1.14 to +5.5) suggest a depleted mantle origin. The Fe-rich dioritic rocks occurring at the margin of massifs have isotopic, chemical and mineral composition more close to anorthosite-mafic-leucomafic rocks. However, there is a gradual decrease in plagioclase content, An content of plagioclase and X_Mg of orthopyroxene, and an increase in mafic silicates, oxide minerals content, plagioclase incompatible elements and REE from anorthosite-mafic-leucomafic rocks to Fe-rich dioritic rocks. The Fe-rich dioritic rocks are interpreted as residual melt from mantle derived high-Al gabbro melt, which produced the anorthosite and mafic-leucomafic rocks. Mineralogically and chemically, the K-rich felsic rocks are distinct from anorthosite-mafic-leucomafic-Fe-rich dioritic suite. They have higher δ ¹⁸O values (6.8–10.8‰) and initial ⁸⁷Sr/⁸⁶Sr (0.7067–0.7104). By contrast, the K-rich felsic suites are products of melting of crustal precursors.