Geochemistry of intrusive rocks associated with the Latir volcanic field,New Mexico,and contrasts between evolution of plutonic and volcanic rocks

Plutonic rocks associated with the Latir volcanic field comprise three groups: 1) 25 Ma high-level resurgent plutons composed of monzogranite and silicic metaluminous and peralkaline granite, 2) 23–25 Ma syenogranite, and alkali-feldspar granite intrusions emplaced along the southern caldera margin, and 3) 19–23 Ma granodiorite and granite plutons emplaced south of the caldera. Major-element compositions of both extrusive and intrusive suites in the Latir field are broadly similar; both suites include high-SiO₂ rocks with low Ba and Sr, and high Rb, Nb, Th, and U contents. Moreover, both intermediateto siliciccomposition volcanic and plutonic rocks contain abundant accessory sphene and apatite, rich in rare-earth elements (REE), as well as phases in which REE's are essential components. Strong depletion in Y and REE contents, with increasing SiO₂ content, in the plutonic rocks indicate a major role for accessory mineral fractionation that is not observed in volcanic rocks of equivalent composition. Considerations of the rheology of granitic magma suggest that accessory-mineral fractionation may occur primarily by filter-pressing evolved magmas from crystal-rich melts. More limited accessory-mineral crystallization and fractionation during evolution of the volcanic magmas may have resulted from markedly lower diffusivities of essential trace elements than major elements. Accessory-mineral fractionation probably becomes most significant at high crystallinities. The contrast in crystallization environments postulated for the extrusive and intrusive rocks may be common to other magmatic systems; the effects are particularly pronounced in highly evolved rocks of the Latir field. High-SiO₂ peralkaline porphyry emplaced during resurgence of the Questa caldera represents non-erupted portions of the magma that produced the Amalia Tuff during caldera-forming eruption. The peralkaline porphyry continues compositional and mineralogical trends found in the tuff. Amphibole, mica, and sphene compositions suggest that the peralkaline magma evolved from metaluminous magma. Extensive feldspar fractionation occurred during evolution of the peralkaline magmas, but additional alkali and iron enrichment was likely a result of high halogen fluxes from crystallizing plutons and basaltic magmas at depth.     

Mineral chemistry and Ti in zircon thermometry: Insights into magmatic evolution of the Sangan igneous rocks,NE Iran

The Sangan Magmatic complex (SMC) is, a large I-type magmatic complex, located in the northeastern Iran. Zircons extracted from the intrusive and volcanic rocks within the SMC record a similar Hf compositions and REE patterns, indicating that these chemical signatures have likely been inherited from the same source and simple history of magmatic crystallization during the evolution of the orogeny. The zircon from volcanic rocks yield Ti-in-zircon crystallization temperatures of 667–1145?°C with average temperatures of 934?°C while those from granitoids indicate crystallization temperatures of 614–898?°C with an average of 812?°C. Ti-in-zircon, Ti in biotite thermometries also indicates that the crystallization temperatures of volcanic rocks are relatively higher than those of granitoids. The biotite chemistry studies reveal that this mineral crystallized at approximately 725°–800?°C and 758° to 816?°C for granitoid and volcanic rocks, respectively, which is similar to obtained temperatures by Zir-saturation of Eq. (1). T_zicsat and T_magma trend lines on the T-SiO₂ diagram cross at high silica contents of ～68?wt.%, at which temperature the magma becomes zircon-saturated and new zircons are crystallized. The zircon REE data including Ce/Ce*, Eu/Eu*, and Th/U ratios suggest that SMC igneous rocks are formed from oxidized magma. However, the zircon Th/U and Hf data suggest that the SMC became progressively more oxidized and also indicate lower temperatures from volcanic and plutonic rock with decreasing time.     

Geochemistry and Geotectonic Setting of Neoproterozoic Rocks from Northern Ethiopia (Arabian-Nubian Shield)

Whole-rock geochemical analysis of metavolcanic and plutonic rocks from Mai Kenetal-Negash area, Tigrai, northern Ethiopia was carried out to evaluate their magma type and original tectonic environment. Their major element content has been modified by secondary alteration, and trace and rare-earth elements have been used to investigate their petrogenesis. The low content of compatible elements of the metavolcanic rocks and their relatively high content of incompatible elements and light REE point to a depleted source region, whereas the plutonic rocks show a more pronounced REE fractionation (La_N/Lu_N >4). Metavolcanic and plutonic rocks seem to be cogenetic. Discriminant diagrams suggest that the majority of the metavolcanic and all the plutonic rocks are members of a calc-alkaline suite developed in a volcanic arc setting. The overall geochemical characteristics of both sets of rocks are consistent with the arc accretion models postulated in Sudan, Egypt and Saudi Arabia for the Neoproterozoic evolution of the Arabian-Nubian Shield.     

REE Geochemical Characteristics of Apatite,Sphene and Zircon from Alkaline Rocks

The accessory minerals apatite and sphene are the main carriers of REE in alkaline rocks.Their chondrite-normalized REE patterns decline sharply to the right as those of the host rocks,In the patterns an obvious negative Eu anomaly and a positive Ce anomaly can be seen in apatite and sphene,respectively.Zircon from alkaline rocks is different in REE pattern,I,e,. a nearly symmetric“V“-shaped pattern with a maximum negative Eu anomaly.Compared with the equivalents from granites,apatite,sphene and zircon from alkaline rocks are all characterized by higher (La/Yb)N ratio and less Eu depletion,As to the relative contents of REE in minerals,apatite,sphene and zircon are enriched in LREE,MREE and HREE respectively,depending on their crystallochemical properties.     

Trace element and isotopic variations in a zoned pluton and associated volcanic rocks,Unalaska Island,Alaska: A model for fractionation in the Aleutian calcalkaline suite

Trace elements, including rare earth elements (REE), exhibit systematic variations in plutonic rocks from the Captains Bay pluton which is zoned from a narrow gabbroic rim to a core of quartz monzodiorite and granodiorite. The chemical variations parallel those in the associated Aleutian calcalkaline volcanic suite. Concentrations of Rb, Y, Zr and Ba increase as Sr and Ti decrease with progressive differentiation. Intermediate plutonic rocks are slightly enriched in light REE (La/Yb=3.45–9.22), and show increasing light REE fractionation and negative Eu anomalies (Eu/Eu^*=1.03–0.584). Two border-zone gabbros have similar REE patterns but are relatively depleted in total REE and have positive Eu anomalies; indicative of their cumulate nature. Initial ⁸⁷Sr/⁸⁶Sr ratios in 8 samples (0.70299 to 0.70377) are comparable to those of volcanic rocks throughout the arc and suggest a mantle source for the magmas. Oxygen isotopic ratios indicate that many of the intermediate plutonic rocks have undergone oxygen isotopic exchange with large volumes of meteoric water during the late stages of crystallization; however no trace element or Sr isotopic alteration is evident.Major and trace element variations are consistent with a model of inward fractional crystallization of a parental high-alumina basaltic magma at low pressures (6 kb). Least-squares approximations and trace element fractionation calculations suggest that differentiation in the plutonic suite was initially controlled by the removal of calcic plagioclase, lesser pyroxene, olivine and Fe-Ti oxides but that with increasing differentiation and water fugacity the removal of sub-equal amounts of sodic plagioclase and hornblende with lesser Fe-Ti oxides effectively drove residual liquids toward dacitic compositions. Major and trace element compositions of aplites which intrude the pluton are not adequately explained by fractional crystallization. They may represent partial melts derived from the island arc crust. Similarities in Sr isotopes, chemical compositions and differentiation trends between the plutonic series and some Aleutian volcanic suites indicates that shallow-level fractional crystallization is a viable mechanism for generating the Aleutian calcalkaline rock series.LDGO Contribution no. 2964     

Geochemical constraints on the genesis of the volcanic rocks in the southeast of Isfahan area, Iran

Late Miocene–Pliocene to Quaternary calc-alkaline lava flows and domes are exposed in southeast of Isfahan in the Urumieh Dokhtar magmatic belt in the Central Iran structural zone. These volcanic rocks have compositions ranging from basaltic andesites, andesites to dacites. Geochemical studies show these rocks are a medium to high K calc-alkaline suite and meta-aluminous. Major element variations are typical for calc-alkaline rocks. The volcanic rocks have SiO₂ contents ranging between 53.8% and 65.3%. Harker diagrams clearly show that the dacitic rocks did not form from the basaltic andesites by normal differentiation processes. They show large ion lithophile elements- and light rare earth elements (LREE)-enriched normalized multielement patterns and negative Nb, Ti, Ta, and P. Condrite-normalized REE patterns display a steep decrease from LREE to light rare earth elements without any Eu anomaly. These characteristics are consistent with ratios obtained from subduction-related volcanic rocks and in collision setting. The melting of a heterogeneous source is possible mechanism for their magma genesis, which was enriched in incompatible elements situated at the upper continental lithospheric mantle or lower crust. The geochemical characteristics of these volcanic rocks suggested that these volcanic rocks evolved by contamination of a parental magma derived from metasomatized upper lithospheric mantle and crustal melts.     

Behavior of rare earth elements in acid coal mine drainage in Shanxi Province, China

Rare earth element (REE) concentrations were determined in acid mine drainage (AMD), bedrock, pyrite, and coal samples from the Sitai coal mine and the Malan coal mine in Shanxi province, China. The AMD displayed high REE concentrations with typical convex shale-normalized patterns. The REE concentrations in the bedrock samples are one order of magnitude higher than those found in pyrite and coal samples. The high REE concentrations in AMD most likely come from the acidic solution leached out REE in bedrock. Results from laboratory and field experiments show that pH is the most important factor controlling the fractionation of REE; but Fe, Al, and Mn colloids and secondary minerals also affects their fractionation. As the pH increased from 4 to 6, the concentrations of total dissolved REE decreased from 520 to 0.875???g?L^?1. Fe and Al in AMD has less influence on the fractionation of dissolved REE than low concentrations of Mn. HREE were preferentially removed by secondary minerals and colloids, followed by MREE. Rare earth element??s speciation modeling indicates that sulfate complexes (LnSO₄ ⁺ and Ln(SO₄) ₂ ^? , 79?C91%) and free-metal species (Ln³⁺, 8.8?C21%) are the dominant REE species in the AMD, but the REE-sulfate complexation could not explain the MREE-enriched patterns.     

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.     

Geochemistry of highly-undersaturated ocean island basalt suites from the South Atlantic Ocean: Fernando de Noronha and Trindade islands

The volcanic rocks of the South Atlantic Ocean islands of Fernando de Noronha and Trindade comprise a diverse magmatic series ranging from nephelinites and basanites to phonolites and, on Fernando de Noronha, trachytes. All rock types are highly silica undersaturated with the exception of Fernando de Noronha trachytes_, and have high abundances of incompatible trace elements and strongly LREE (light rare earth element)-enriched REE patterns. Crystal fractionation of parental basanitic magmas produced evolved phonolites and trachytes which display severe trace-element fractionation, even among trace elements (Nb, Ta, Zr, Hf) which normally behave highly incompatibly during crystallisation of alkaline magmas. Moderately to highly evolved compositions develop strongly MREE (middle REE)-depleted REE patterns, and become increasingly depleted in elements such as Nb and, in particular, Ta. Ratios of Nb/Ta and Zr/Hf are highly fractionated in phonolites (60–65, 64–77 respectively in Fernando de Noronha phonolites) compared to ratios in basanites (14, 45 respectively). The compatibility of Nb, Ta, and the REE, and the strong fractionation of Nb/Ta and Zr/Hf ratios and the MREE, during crystallisation from basanite to phonolite are attributable to the crystallisation of small amounts (<5%) of sphene. Trace-element behaviour is relatively insensitive to the major phenocryst phases, and is controlled by minor phases in highly undersaturated alkaline suites. Incompatible trace-element ratios (e.g. La/Nb, Th/Ta) in nephelinites and basanites from Fernando de Noronha and Trindade are generally comparable with those in basaltic and hawaiitic OIB (ocean island basalt) lavas from other South Atlantic islands, but are distinct from those of Gough and Tristan da Cunha OIB. The mantle source for the highly undersaturated volcanism on Fernando de Noronha and Trindade is similar in trace-element characteristics to the typical OIB source which produces alkaline lavas with significant relative enrichment in Nb and Ta compared to other trace elements (as expressed by low La/Nb, Ba/Nb and Th/Ta ratios). The highly undersaturated nature of the magmas and the slight fractionation of some incompatible-element ratios (elevated Ba/Nb, Ba/Rb, Ba/Th etc.) is consistent with a smaller degree of melting of a typical OIB source, but with residual phlogopite in the source to account for significant K depletion and LIL-element fractionation.     

Rare earth geochemistry in the dissolved, suspended and sedimentary loads in karstic rivers, Southwest China

The watershed in the central Guizhou Province (Guizhou Province is called simply Qian) (CQW) is a karstic area. Rare earth elements (REEs) of dissolved loads, suspended particulate material (SPM) and sediments of riverbed are first synthetically reported to investigate REE geochemistry in the three phases in karstic watershed during the high-flow season. Results show that the low dissolved REE concentrations in the CQW are attributed to these rivers draining carbonate rocks. The dissolved REE have significant negative Eu anomaly and coexistence of middle and light REE (MREE??PAAS-normalized La _N /Sm _N and Gd _N /Yb _N ; LREE??PAAS-normalized La _N /Yb _N )-enrichment, which are due to the dissolution of impure Triassic carbonates. REE concentrations in most of SPM exceed that of sediments in the CQW and the average continental crust (UCC). The SPM and the sediments show some common features: positive Eu, Ce anomalies, and MREE enrichment. The controls on the patterns seem to be from weathering profiles: the oxidation state, the REE-bearing secondary minerals (cerianite, potassium feldspar and plagioclase), which are also supported by the evidence of Y/Ho fractionations in the three phases.     

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.     

Geochemistry of trace and rare earth elements during weathering of black shale profiles in Northeast Chongqing,Southwestern China: Their mobilization,redistribution, and fractionation

In this study, the mobilization, redistribution, and fractionation of trace and rare earth elements (REE) during chemical weathering in mid-ridge (A), near mountaintop (B), and valley (C) profiles (weak, weak to moderate, and moderate to intense chemical weathering stage, respectively), are characterized. Among the trace elements, U and V were depleted in the regolith in all three profiles, Sr, Nb, Ta, Zr, and Hf displayed slight gains or losses, and Th, Rb, Cs, and Sc remained immobile. Mn, Ba, Zn, Cu, and Cr were enriched at the regolith in profiles A and B, but depleted in profile C. Mn, Pb, and Co were also depleted in the saprock and fractured shale zones in profiles A and B and enriched in profile C. REEs were enriched in the regolith and depleted at the saprock zone in profiles A and B and depleted along profile C. Mobility of trace and REEs increased with increasing weathering intensity. Normalized REE patterns based on the parent shale revealed light REE (LREE) enrichment, middle REE (MREE), and heavy REE (HREE) depletion patterns. LREEs were less mobile compared with MREEs and HREEs, and this differentiation increased with increasing weathering degree. Positive Ce anomalies were higher in profile C than in profiles A and B. The Ce fractionated from other REE showed that Ce changed from trivalent to tetravalent (as CeO₂) under oxidizing conditions. Minimal REE fractionation was observed in the saprock zone in profiles A and B. In contrast, more intense weathering in profile C resulted in preferential retention of LREE (especially Ce), leading to considerable LREE/MREE and LREE/HREE fractionation. (La/Yb)_N and (La/Sm)_N ratios displayed maximum values in the saprock zone within low pH values. Findings demonstrate that acidic solutions can mobilize REEs and result in leaching of REEs out of the highly acidic portions of the saprock material and transport downward into fractured shale. The overall behavior of elements in the three profiles suggests that solution pH, as well as the presence of primary and secondary minerals, play important roles in the mobilization and redistribution of trace elements and REEs during black shale chemical weathering.     

Paleozoic alkaline volcanism: geochemistry and petrogenesis of Um Khors and Um Shaghir trachytes of the central Eastern Desert, Egypt

The Um Khors and Um Shaghir trachyte (UKT and UST) plugs and sheets represent two conspicuous outcrops of Paleozoic alkaline volcanism in the central Eastern Desert of Egypt. The trachyte magmatisms erupted along the Pan-African NW-trending shear zone (302?±?15 and 273?±?15?Ma, respectively) and intruded the Late Proterozoic rocks of the studied area. The trachyte rocks consist mainly of sanidine, anorthoclase, albite, and quartz with a noticeable amount of aegirine?Caugite, aegirine, hedenbergite, and arvedsonite. The studied trachytes are moderately evolved in composition (with 62?C67.5?wt.% SiO₂) and exhibit a limited compositional range in most of the major elements. They are alkaline in nature and considered as silica-oversaturated rocks. The rare earth elements (REE) patterns are somewhat uniform and highly fractionated, being enriched in light REE over heavy REE and show prominent negative Eu anomalies. The UKT and UST are enriched in high field strength elements Nb, Zr, and Y, consistent with typical within-plate alkaline magmatisms of extensional tectonic regimes. They were generated through the fractional crystallization of mantle-derived magmas. Although the UST is younger than the UKT, they show approximately similar chemical compositional ranges of the most major and trace elements, with somewhat higher MgO, Cr, Ni, and Ba contents in the former. This may argue against the evolution of the UST via a continuous fractional crystallization of the residual magmatic melt of the UKT. Thus, the UKT and UST are genetically related but could be emplaced through two various magmatic pulses of the same parent source (i.e., asthenospheric mantle source) at different times. The ascending magmatisms were subjected to variable significant degrees of crustal contamination during their generation.     

大兴安岭北段图里河地区满克头鄂博组火山岩年代学及地球化学

对大兴安岭北段图里河地区满克头鄂博组火山岩进行了锆石U-Pb年代学及岩石地球化学研究,以便对其岩石成因和构造背景给予制约。流纹岩LA-ICP-MS锆石U-Pb定年结果表明,该地区满克头鄂博组火山岩形成时代为晚侏罗世(157±1Ma)。该组火山岩具有高硅(Si O2=69.09%~75.92%)、富碱(K2O+Na2O=8.04%~9.23%),贫镁、铁、钙的特征,属高钾钙碱性、偏铝质-弱过铝质岩石;稀土元素配分曲线呈轻稀土富集的右倾形式,(La/Yb)N=5.85~13.53,无铕异常或具有较弱的铕负异常;火山岩样品富集Rb、Th、U、K等大离子亲石元素,亏损Nb、Ta、Ti等高场强元素。Mg#值为12.14~31.01,平均值22,Nb/Ta值(6.67~27.17,平均值12.23),Rb/Sr值(0.35~3.63,平均值1.58),显示火山岩岩浆源区为下地壳。依据岩石地球化学特征、构造判别图解,结合区域构造演化特征,认为满克头鄂博组火山岩形成于蒙古—鄂霍茨克洋闭合的造山后伸展背景。     

Geochemical and mineralogical characteristics of recent clastic sediments from lower Godavari river: Implications of source rock weathering

The major, trace and rare earth elements geochemistry and clay mineral compositions in the river bed sediments from lower reaches of Godavari river suggest that they are derived from weathering of felsic rocks. Trace and rare earth elemental compositions indicate evidence of sedimentary sorting during transportation and deposition. Lower concentrations of transition elements, such as V, Ni and Cr imply enrichment of felsic minerals in these bed sediments. The REE pattern in lower Godavari sediments is influenced by the degree of source rock weathering. The light rare earth elements (LREE) content are indicating greater fractionation compared to the heavy rare earth elements (HREE). A striking relationship is observed between TiO₂ and gZREE content suggesting a strong control by LREE-enriched titaniferous minerals on REE chemistry. Shale-normalized REE pattern demonstrate a positive Eu anomaly, suggesting weathering of feldspar and their secondary products, which are enriched in Eu. Chondrite-normalised REE pattern is characteristic of felsic volcanic, granites and gnessic source rocks. Trace elemental compositions in sediments located near urban areas suggest influence of anthropogenic activity. Chemical Index of Alteration (CIA) is high (avg. 65.76), suggesting a moderate chemical weathering environment. X-ray diffraction analysis of clay fraction shows predominance of clay minerals that are formed because of the chemical weathering of felsic rocks.     

REE systematics of fluorides,calcite and siderite in peralkaline plutonic rocks from the Gardar Province,South Greenland

The Gardar failed-rift Province is world-famous for its (per-)alkaline plutonic rocks. Elevated contents of F in the mantle source and F-enrichment in the parental melts have been suggested to account for the peculiarities of the Gardar rocks (e.g. their rare mineralogy, extreme enrichment of HFSE elements, Be or REE in the Ilímaussaq agpaites, and the formation of the unique Ivigtut cryolite deposit). To constrain the formation and chemical evolution of F-bearing melts and fluids, fluorides (fluorite, cryolite, villiaumite, cryolithionite), calcite and siderite from the Ilímaussaq, Motzfeldt and Ivigtut complexes were analysed for their trace element content focusing on the rare earth elements and yttrium (REE).The various generations of fluorite occurring in the granitic Ivigtut, agpaitic Ilímaussaq and miaskitic to agpaitic Motzfeldt intrusions all share a negative Eu anomaly which is attributed to (earlier) feldspar fractionation in the parental alkali basaltic melts. This interpretation is supported by the abundance of anorthositic xenoliths in many Gardar plutonic rocks.The primary magmatic fluorites from Ilímaussaq and Motzfeldt display very similar REE patterns suggesting a formation from closely related parental melts under similar conditions. Hydrothermal fluorites from these intrusions were used to constrain the multiple effects responsible for the incorporation of trace elements into fluorides: temperature dependence, fluid migration/interaction and complexation resulting in REE fractionation. Generally, the REE patterns of Gardar fluorides reflect the evolution and migration of a F/CO₂-rich fluid leading to the formation of fluorite and fluorite/calcite veins. In certain units, this fluid inherited the REE patterns of altered host rocks. In addition, there is evidence of an even younger fluid of high REE abundance which resulted in highly variable REE concentrations (up to three orders of magnitude) within one sample of hydrothermal fluorite.The REE patterns of the granitic Ivigtut intrusion show flat to slightly heavy-REE-enriched patterns characterised by a strong tetrad effect. This effect is interpreted to record extensive fluid–rock interaction in highly fractionated, Si-rich systems.Interestingly, the fluorides appear to record different source REE patterns, as the spatially close Motzfeldt and Ilímaussaq intrusions show strong similarities and contrast with the Ivigtut intrusion located 100 km NE. These variations may be attributed to differences in the tectonic position of the intrusions or mantle heterogeneities.     

Geochemistry and petrogenesis of Neoproterozoic A-type granites at Nakora in the Malani Igneous Suite, Western Rajasthan, India

The Nakora Ring Complex(NRC)(732 Ma) occurs as a part of Malani Igneous Suite(MIS) in the West-ern Rajasthan,India.This complex consists of three phases(volcanic,plutonic and dyke).Geochemically,the Na-kora granites are peralkaline,metaluminous and slightly peraluminous.They display geochemical characteristics of A-type granites and distinct variation trends with increasing silica content.The peralkaline granites show higher concentrations of SiO2,total alkalies,TiO2,MgO,Ni,Rb,Sr,Y,Zr,Th,U,La,Ce,Nd,Eu and Yb and lower concen-trations of Al2O3,total iron,Cu and Zn than metaluminous granites.AI content is ≥1 for peralkaline granites and <1 for peraluminous and metaluminous granites.Nakora peralkaline granites are plotted between 4 to 7 kb in pressure and are emplaced at greater depths(16-28 km and 480-840℃) as compared to metaluminous granites which indicate the high fluorine content in peralkaline granites.The primitive mantle normalized multi-element profiles suggest that Nakora granites(peralkaline,metaluminous and peraluminous) are characterized by low La,Sr and Eu and relatively less minima of Ba,Nb and Ti which suggests the aspects related to crustal origin for Nakora magma.The Nakora granites are characterized as A-type granites(Whalen et al.,1987) and correspond to the field of "Within Plate Gran-ite"(Pearce et al.,1984).Geochemical,field and petrological data suggest that Nakora granites are the product of partial melting of rocks similar to Banded Gneiss from Kolar Schist Belt of India.     

Geochemistry and fluid evolution of the peralkaline rare-metal granite, Gabal Gharib, Eastern Desert of Egypt

The Neoproterozoic pluton of Gabal Gharib granite Eastern Desert of Egypt is intruded in subduction-related calc-alkaline granitic rocks of granodiorite to adamellite composition. A zone of metasomatized granite was developed along the contacts at the expense of the calc-alkaline granite. The granite of Gabal Gharib is hypersolvus, composed mainly of orthoclase-microperthite, quartz, and interstitial arfvedsonite. Fluorite, zircon, ilmenite, allanite, and astrophyllite are the main accessories. Pegmatite pods as well as miarolitic cavities (mineral-lined cavities) are common and ranging in size from a few millimeters to 50?cm. Rare-metal minerals such as columbite, cassiterite, and fluorite have been identified from the miarolitic cavities. Geochemical studies revealed that Gabal Gharib granite is a highly fractionated granite, homogeneous in composition, with high contents of SiO₂, and alkalis, high Ga/Al, and Fe/Mg ratios, and low concentrations of Al, Mg, and CaO relative to granodiorite?Cadamellite country rocks. Gabal Gharib granite is metaluminous to peralkaline with ASI (0.94?C1.07). Trace element characteristics of Gabal Gharib granite include abundances of Rb, Nb, Ta, Sn, Th, U, Y, Ga, Zn, rare earth elements (REEs, except Eu), and F, and depletion in Sr, and Ba relative to granodiorite?Cadamellite country rocks. It has the geochemical characteristic of anorogenic A-type granite. The uniform trends of differentiation, normal REE distribution patterns, and low calculated tetrad effects of REE (<0.2) indicate that the effect of post-magmatic subsolidus processes were minimal in the studied granite. Fluid inclusions were studied in quartz crystals from Gabal Gharib granite, quartz pods, and metasomatized granite. The study revealed the presence of high-temperature (480?C550°C), high-salinity (19.45?C39.13?wt.% NaCl eq.) primary inclusions in both metasomatized and rare-metal granites coexisting with melt inclusions and medium-temperature (350?C450°C), medium-salinity (10?C16?wt.% NaCl esq.) aqueous inclusions coexisting hydrocarbon-bearing inclusions. Hydrocarbon is represented by magmatic CH4 in Gabal Gharib granite, while heavier aliphatic compounds may be present in quartz pods. Melt inclusions with temperatures of homogenization >600°C were also reported. Petrographic, geochemical, and fluid inclusion studies constrain that the peralkaline anorogenic granite of Gabal Gharib was derived from highly evolved magma probably originated by fractional crystallization of mantle source.     

REE in charnockite and associated rocks,southwest Sweden

The rate earth element compositions of a suite of high-grade metamorphic and plutonic rocks which outcrop in the Varberg region of southwest Sweden are presented. A plutonic complex containing both charnockitic and non-charnockitic elements intrudes country rocks of upper amphibolite and granulite facies grade. The REE data for the country rocks sustain the view that they are supracrustal origin and support the importance placed on these elements in investigations of metamorphic rock progenitors. The progressive change in REE characteristics found for the various units of the plutonic association confirms that they represent rational stages in differentiation from a common parent. The end-product of this differentiation is a granite with the REE concentration and distribution found, elsewhere in the Baltic Shield, to characterize Rapakivi granite. The progressive change in REE with time suggested for the Baltic Shield by other authors finds support in the results of this study.     

白头山火山渣锥的岩浆演化研究

火山渣锥是白头山(或长白山)火山喷发的重要产物,主要沿熔岩台地周边呈圆锥状寄生小火山锥体分布。野外特征显示,火山渣是火山渣锥的重要组成;岩石手标本显示,火山渣具有气孔构造,样品自顶部至底部,颜色从赤色、赤褐色,向褐色、灰色发生转变。地球化学特征表明,火山渣岩性包括玄武岩、粗面玄武岩、玄武岩质粗面安山岩、粗面安山岩岩,具有较高SiO_2(46.22%~55.38%),Al_2O3含量(15.28%~22.11%),低MgO(2.05%~4.94%),FeOT(6.79%~14.76%)的特征;同时具有较高的碱Na_2O/K_2O(Na_2O/K_2O1)比值,为钠质火山岩。其轻稀土(LREE)和重稀土(HREE)分异明显,具有弱的δEu正异常,并且具有富集K、Rb、Ba、Sr等大离子亲石元素(LILE)和相对亏损Nb、Ti等高场强元素(HFSE)的特征。此外,火山渣的分异指数(DI)范围为36.93~64.48,高于造盾阶段的幔源玄武岩的分异指数;其固结指数(SI)为10.73~24.09,低于早期幔源玄武岩的固结指数(SI=25~45),这些特征说明火山渣成分发生了较高程度的岩浆分异作用。同时,火山渣的Nb/La、Sm/Nd、La/Nb和Ba/Nb比值几乎全部介于幔源玄武岩和大陆地壳之间,说明具有明显的地壳混染的特征。因此,我们认为研究区火山渣的岩浆可能是由幔源基性玄武岩上升过程中发生分离结晶和地壳混染作用形成的。