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1.
A 1500 m thick sheet-like body of ferroaugite syenite is divisiblemineralogically into an upper and lower series of syenites.The lower syenites are characterized by well developed igneouslayering defined by mafic cumulus minerals. The syenites aresaturated to oversaturated and contain as cumulus phases alkalifeldspar, olivine (Fa83–93), ferroaugite (Di50Hd45Ac5–Di5Hd90Ac5)and ilmeno-magnetite. Amphiboles which crystallized from theintercumulus liquid range in composition from ferrohastingsitichornblende to ferroedenitic hornblende to ferroactinolitic edenite.The upper series are coarse grained cumulates with poorly definedlayering and abundant patch pegmatites. Cumulus phases are alkalifeldspar, olivine (Fa93), and acmitic-hedenbergite (Di5Hd50Ac5–Ac50Hd50).Intercumulus liquids are peralkaline and crystallized to aenigmatiteand amphiboles which range in composition from ferrorichteritickatophorite to ferrorichterite, Patch pegmatites are peralkalinerocks composed of ferrorichterite, ferroactinolite, alkali feldspar,aenigmatite, quartz and zircon. Extreme differentiation of ferroaugitesyenite magma generates residua which are ironrich, oversaturatedand peralkaline. Initial and final temperatures of crystallizationare estimated from mineral stability data to be 800–900°C to 500–550 °C respectively. Thermodynamic dataand mineral compositions indicate that during crystallizationthe oxygen fugacity of the magma decreased from approximately10–15 to 10–23–10–24 bars. Ferroaugitesyenite pyroxene compositional trends are similar to those ofundersaturated peralkaline syenites (llimaussaq) and demonstratethat acmite enrichment trends are independent of silica activityand take place under decreasing oxygen fugacities.  相似文献   

2.
The Cretaceous Banhad?o alkaline complex in southeastern Brazil presents two potassic SiO2-undersaturated series. The high-Ca magmatic series consist of initially fractionated olivine (Fo92-91) + diopside (Wo48-43En49-35Ae0-7), as evidenced by the presence of xenocrysts and xenoliths. In that sequence, diopside (Wo47-38En46-37Ae0-8) + phlogopite + apatite + perovskite (Prv>92) crystallized to form the phlogopite melteigite and led to the Ca enrichment of the magma. Diopside (Wo47-41En32-24 Ae3-14) continued to crystallize as an early mafic mineral, followed by nepheline (Ne74.8-70.1Ks26.3-21.2Qz7.6-0.9) and leucite (Lc65-56) and subsequently by melanite and potassic feldspar (Or85-99Ab1-7) to form melanite ijolites, wollastonite-melanite urtites and melanite-nepheline syenites. Melanite-pseudoleucite-nepheline syenites are interpreted to be a leucite accumulation. Melanite nephelinite dykes are believed to represent some of the magmatic differentiation steps. The low-Ca magmatic series is representative of a typical fractionation of aegirine-augite (Wo36-29En25-4Ae39-18) + alkali feldspar (Or57-96Ab3-43) + nepheline (Ne76.5-69.0Ks19.9-14.4Qz15.1-7.7) + titanite from phonolite magma. The evolution of this series from potassic nepheline syenites to sodic sodalite syenites and sodalitolites is attributed to an extensive fractionation of potassic feldspar, which led to an increase of the NaCl activity in the melt during the final stages forming sodalite-rich rocks. Phonolite dykes followed a similar evolutionary process and also registered some crustal assimilation. The mesocratic nepheline syenites showed interactions with phlogopite melteigites, such as compatible trace element enrichments and the presence of diopside xenocrysts, which were interpreted to be due to a mixing/mingling process of phonolite and nephelinite magmas. The geochemical data show higher TiO2 and P2O5 contents and lower SiO2 contents for the high-Ca series and different LILE evolution trends and REE chondrite-normalized patterns as compared to the low-Ca series. The 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb and 208Pb/204Pb initial ratios for the high-Ca series (0.70407–0.70526, 0.51242–0.51251, 17.782–19.266 and 38.051–39.521, respectively) were slightly different from those of the low-Ca series (0.70542–0.70583, 0.51232–0.51240, 17.758–17.772 and 38.021–38.061, respectively). For both series, a CO2-rich potassic metasomatized lithospheric mantle enriched the source with rutile-bearing phlogopite clinopyroxenite veins. Kamafugite-like parental magma is attributed to the high-Ca series with major contributions from the melting of the veins. Potassic nephelinite-like parental magma is assigned to the low-Ca series, where the metasomatized wall-rock played a more significant role in the melting process.  相似文献   

3.
The igneous alkaline rocks at Elchuru start from a parent ijolite-melteigite association to basic malignite, melalusitanite and shonkinite followed by nepheline syenites and then biotite lamprophyres (as dykes) at the waning phase of the evolutionary course of the complex. The distinct alkalinity of the rocks is manifested by the development of modal nepheline and calcic amphibole (kaersutite). For both the basic rocks,i.e. alkali gabbro and biotite lamprophyre, the percentages of normative nepheline are always higher than modal nepheline, indicating silica deficiency and alkali enrichment of the mafics. It is evident from detailed petrological and geochemical studies that the two basic members are very much akin to each other and there is no major deviation in their bulk chemistry.  相似文献   

4.
Seven pyroxene varieties were identified in nepheline syenites and foidolites of the Khibiny pluton: enstatite, ferrosilite, diopside, hedenbergite, augite, aegirine-augite, and aegirine. Enstatite and augite are typical of alkaline and ultramafic rocks of dike series. Ferrosilite was found in country quartzitic hornfels. Diopside is a rock-forming mineral in alkaline and ultramafic rocks, alkali gabbroids, hornfels in xenoliths of volcanic and sedimentary rocks and foyaite, melteigite-urtite that assimilate them, and certain hydrothermal pegmatite veins. Hedenbergite was noted in hornfels from xenoliths of volcanic and sedimentary rocks and in a hydrothermal pegmatite vein at Mount Eveslogchorr. Aegirine-augite is the predominant pyroxene in all types of nepheline syenites, phonolites and tinguaites, foidolites, alkaline and ultramafic rocks of dike series, fenitized wall rocks surrounding the pluton, and xenoliths of Devonian volcanic and sedimentary rocks. Aegirine is an abundant primary or, more often, secondary mineral in nepheline syenites, foidolites, and hydrothermal pegmatite veins. It occurs as separate crystals, outer zones of diopside and aegirine-augite crystals, and homoaxial pseudomorphs after Na-Ca amphiboles. Microprobe analyses of 265 pyroxenes samples allowed us to distinguish ten principal trends of isomorphic replacement and corresponding typomorphic features of pyroxenes. Compositional variations in clinopyroxenes along the sampled 35-km profile from the margin of the Khibiny pluton to its center confirm the symmetric zoning of the foyaite pluton relative to semicircular faults of the Minor Arc and the Main (Central) Ring marked by Devonian volcanic and sedimentary rocks, foidolites, and related metasomatic rocks (rischorrite, albitite, and aegirinite). Changes in the composition of pyroxenes are explained mainly by the redistribution of elements between coexisting minerals of foyaites in the process of their intense differentiation under the effect of foidolite melts that have intruded into the circular fault zones.  相似文献   

5.
Aegirines with almost 7.0 wt.% ZrO2 have been discovered in nepheline syenites from the Motzfeldt Centre, South Greenland. The analyses require the postulate of a new endmember pyroxene composition with the formula NaFM0.5Zr0.5Si2O6.A possible acronym is FM-NAZ. Aegirines rich in this component occur in rocks in which there is no other zirconium-bearing phase such as eudialyte.These zirconian pyroxenes have crystallised from magmas which were peralkaline, low in lime and silica and relatively low in oxygen fugacity compared with other nepheline syenites. These factors have combined to prevent the usual crystallisation of such Zr-phases as eudialyte, zircon or baddeleyite.  相似文献   

6.
Aegirines with almost 7.0 wt.% ZrO2 have been discovered in nepheline syenites from the Motzfeldt Centre, South Greenland. The analyses require the postulate of a new endmember pyroxene composition with the formula NaFM0.5Zr0.5Si2O6.A possible acronym is FM-NAZ. Aegirines rich in this component occur in rocks in which there is no other zirconium-bearing phase such as eudialyte.These zirconian pyroxenes have crystallised from magmas which were peralkaline, low in lime and silica and relatively low in oxygen fugacity compared with other nepheline syenites. These factors have combined to prevent the usual crystallisation of such Zr-phases as eudialyte, zircon or baddeleyite.  相似文献   

7.
华北克拉通北缘晚志留世末-早泥盆世碱性岩的成因研究可以为古生代古亚洲洋与华北克拉通的相互作用过程提供重要信息。本文以内蒙古达茂旗黄合少正长岩为研究对象,开展了锆石U-Pb年代学、矿物化学、地球化学和Sr-Nd同位素的研究,并综合同带其他代表性岩体的岩石矿物及元素特征,探讨了华北克拉通北缘钾质碱性岩的岩浆体系性质、源区特征及构造动力学背景。黄合少正长岩的主要岩石类型为碱性长石正长岩,锆石SHRIMP U-Pb年龄为417.6±4.7 Ma,为晚志留世末期岩浆作用的产物;主要组成矿物为霓辉石和钾长石(An_0Ab_(2～5)Or_(95～98))及少量钠长石(An_0Ab_(95～100)Or_(0～5)),可见霓辉石内部部分转化为蓝透闪石或镁钠闪石;黄合少正长岩具有较高的全碱含量(Na_2O+K_2O=12.79%～15.30%)和里特曼指数(8.48～11.09),较高的K_2O含量(8.66%～13.78%)和K_2O/Na_2O值(2.10～9.07),指示黄合少正长岩属于钾质-超钾质碱性岩系列;较高的Sr含量和富集放射性成因的Sr同位素组成(初始~(87)Sr/~(86)Sr值为0.704 1～0.706 1),显示岩体起源于被俯冲沉积物交代过的富集岩石圈地幔。华北克拉通北缘晚志留世末-早泥盆世钾质碱性岩的发育,指示早古生代期间发育古亚洲洋板片向华北克拉通下的俯冲,俯冲相关物质对华北克拉通岩石圈地幔进行交代,形成含金云母/角闪石等交代矿物的易熔地幔;晚志留世末-早泥盆世时,由于微陆块的拼贴碰撞,华北克拉通北缘暂时处于碰撞后伸展演化阶段。  相似文献   

8.
The Itatiaia alkaline complex is a Late Cretaceous intrusion (72 Myr) made up of felsic differentiates, with syenitic rocks dominant throughout and with presence of both nepheline- and quartz-rich varieties. Dykes with phonolitic or trachytic composition cross-cut the coarse-grained facies. The rocks are arranged concentrically, with the core of the complex being formed by SiO2-oversaturated syenites (with a small outcrop of granites), and are radially displaced by faults related to regional tectonic lineaments. The minerals show gradual but significant changes in composition (salitic and augitic to aegirine-rich pyroxenes, hastingsite and actinolite to richterite and arfvedsonite amphiboles, sodic plagioclase to orthoclase feldspars and so on) and the whole-rock trends are broadly consistent with fractional crystallization processes dominated by alkali feldspar removal. Sr-isotopic data indicate more radiogenic ratios for the SiO2-oversaturated rocks (0.7062-0.7067 against 0.7048-0.7054 for the SiO2-undersaturated syenites), consistent with small amounts of crustal input. The favored hypothesis for the petrogenesis of the different syenitic groups is the prolonged differentiation starting from differently SiO2-undersaturated mafic parental magmas (potassic alkali basalts to ankaratrites, present in the Late Cretaceous dyke swarms of the area), accompanied by variable crustal contamination prior to the final emplacement. The lack of carbonatite as a significant lithotype, the potassic affinity of the Itatiaia complex, and the relatively high Sr-isotopic ratios match the characteristics of the other complexes of the Rio de Janeiro-Sa˜o Paulo states coastline and confirm the ultimate derivation of these differentiated rocks from an enriched lithospheric mantle source.  相似文献   

9.
At Gordon Butte (Crazy Mountains, Montana), agpaitic nepheline-syenite pegmatites intrude potassic alkaline rocks (principally, malignites and nepheline microsyenites). All pegmatite veins are composed predominantly of potassium feldspar, nepheline, prismatic aegirine, barytolamprophyllite, wadeite, eudialyte, loparite-(Ce) and altered rinkite ("vudyavrite") embedded in spherulitic and fibrous aegirine. Well-differentiated veins contain "pockets" filled with calcite, fluorapatite, mangan-neptunite, Mn-Ti-enriched prismatic aegirine, calcium catapleiite, and an unidentified Ca-Ti silicate. The potassium feldspar corresponds to Ba-rich sanidine with relatively low Na contents. The nepheline contains low levels of SiO2 and elevated Fe contents. The compositions of nepheline cluster in the lower portion of the Morozewicz-Buerger convergence field, indicating low-temperature crystallization and/or chemical re-equilibration of this mineral. The association of sanidine with nearly stoichiometric nepheline is unusual for agpaitic rocks and probably reflects inhibition of Al/Si ordering in the feldspar by Ba. At least four types of clinopyroxene can be distinguished on the basis of their morphology and composition. All these types correspond to Al- and Ca-poor aegirine (typically <0.6 and 2.6 wt% Al2O3 and CaO, respectively). The overall evolutionary trend of clinopyroxene in the Gordon Butte rocks is from Fe-poor diopside to aegirine-augite in the malignites and nepheline microsyenites, and culminates with the pegmatitic aegirine. This trend is characteristic for potassic alkaline complexes and results from preferential partitioning of Fe2+ into biotite during the magmatic crystallization. Barytolamprophyllite in the pegmatites is primary (as opposed to deuteric); only a few crystals contain a core composed of lamprophyllite. The evolutionary history of the Gordon Butte pegmatites can be subdivided into primary, agpaitic, and deuteric stages. The earliest paragenesis to crystallize included accessory zircon and thorite. Sr-rich loparite also precipitated relatively early serving as a major repository for Sr, REE, and Nb. During the agpaitic stage, diverse titano- and zircono-silicates (barytolamprophyllite, eudialyte, wadeite, and rinkite, among others) consumed most of the Ba, Sr, Ti, Zr, and Nb still remaining in the melt. The final stage in the evolution of the pegmatites involved interaction of the earlier-formed mineral assemblages with deuteric fluids. In common with the Rocky Boy pegmatites, Sr-REE-Na-rich fluorapatite, Ba-Fe titanates and REE-bearing carbonates (ancylite, calcio-ancylite, and bastnäsite-parisite series) are chief products of the deuteric stage. The alteration of the primary mineral assemblages by deuteric fluids also produced muscovite-zeolite pseudomorphs after nepheline, replacement of wadeite and eudialyte by catapleiite-group minerals, re-deposition of Ba in the form of hyalophane, baotite, and benitoite, and cation leaching from rinkite, eudialyte, and loparite. The mineralogy of the pegmatites from Gordon Butte, other potassic complexes, and sodic agpaitic occurrences is compared in detail.  相似文献   

10.
付家山矽卡岩钨矿床位于长江中下游成矿带鄂东矿集区,矿体产于晚中生代花岗闪长斑岩体与下二叠统含碳质地层的接触带。付家山矿区西侧地层为茅口组灰岩,东侧地层为栖霞组灰岩,茅口组灰岩中有机碳含量(0.72%)低于栖霞组灰岩(0.95%)。为了探明不同地层对矽卡岩钨矿床的矿物成分的影响,文章针对付家山矽卡岩钨矿的地层、矽卡岩矿物和白钨矿进行详细地野外地质观察和编录,并利用电子探针(EMPA)开展矿物成分分析。东、西侧地层中矽卡岩阶段的石榴子石和辉石有明显差异,与茅口组接触交代形成的石榴子石变化范围较小(And_(31～90)Gro_(1～53)Spr_(5～20)),辉石端员成分变化范围变化较大(Di_(0～100)Hd_(0～97));而与栖霞组接触交代形成的石榴子石变化范围较大,主要为And_(66～95)Gro_(0～27)Spr_(3～7),部分为And_(19～33)Gro_(60～76)Spr_(3～7)。辉石端员成分为Di_(44～64)Hd_(29～49(。西侧矿段石英-硫化物阶段和方解石阶段中白钨矿的MoO_3相较于东侧矿段含量要高,产于茅口组矿体的石英-硫化物和方解石阶段白钨矿w(MoO_3)为0～1.82%,产于栖霞组矿体的石英-硫化物和方解石阶段白钨矿w(MoO_3)为0.08%～0.86%。上述矿物组合暗示付家山西侧矿段相较于东侧矿段形成环境更为氧化,表明含碳量不同的地层对矽卡岩钨矿的形成有明显的影响。  相似文献   

11.
An early Cretaceous alkaline ultramafic-mafic complex is emplaced within the Proterozoic rocks of Shillong plateau at Jasra, Karbi Anglong district of Assam. It is associated to the fracture system of Barapani-Tyrsad shear zone, Kopali faults, and Um Ngot lineaments and mainly comprises pyroxenite, gabbro and nepheline syenite. Few small mafic dykes, emplaced within pyroxenitic and granitic plutons, are also reported. No such dyke is reported to cut gabbros or nepheline syenites. Nepheline syenites occur either in the form of small dykes in pyroxenites or as differentiated bodies in the gabbros. Mineralogical and chemical composition of pyroxenite and gabbro clearly indicate their affinity to the alkaline magmatism. Syenitic samples show miaskitic character (agpaitic index <1), also indicates affinity with alkaline-carbonatite magmatism. Calcite is encountered in a number of pyroxenite samples. From the presented petrological and geochemical data it is difficult to establish any significant genetic relationship through simple differentiation process between these rocks. These data probably suggest that these rocks are derived from a primary carbonatite magma, generated by the low-degree melting of a metasomatized mantle peridotite. CO2 released by this process also progressively metasomatizes the lherzolite to an alkaline wehrlite and melts derived from alkaline wehrlite (ultrabasic alkaline silicate magma) may be responsible for crystallization of Jasra alkaline ultramafic-mafic rocks.  相似文献   

12.
LA-ICP MS data are presented for ilmenites from different rocks of the alkaline complexes of the Ukrainian Shield (Chernigovka carbonatite, Oktyabr’skii, Malaya Tersa, and Southern Kal’chinskii gabbrosyenite massifs). Ilmenites from the early intrusive phases (alkaline pyroxenites, gabbroids, and ultramafic rocks) have the elevated contents of Cr, Co, Ni, and V, while ilmenites from later alkaline and nepheline syenites, monzonites, and carbonatites are significantly enriched in Nb and Ta, which is caused by change in the alkalinity of the mineral-forming medium. Zr shows the more intrinsic behavior: its content is higher in the ilmenites from basic and ultrabasic rocks than in those from the nepheline syenites and carbonatites. This is mainly caused by temperature conditions of the formation of differentiated alkaline complexes. The carbonatites contain magnesian ilmenite (up to 22 mol % MgTiO3). Variations of Mg contents in ilmentes are correlated with Mg number of mafic minerals and depend also on the iron oxidation state (amount of magnetite) in the carbonatites. In the alkaline massifs of the Ukrainian Shield, ilmenites usually have the low contents of hematite end member (3–7 mol %). Ilmenite serves as a sensitive indicator of temperature, oxygen fugacity, and alkalinity of the mineral-forming medium during crystallization.  相似文献   

13.
The Dongping gold deposit hosted in syenites is one of the largest hydrothermal gold deposits in China and composed of ore veins in the upper parts and altered zones in the lower parts of the ore bodies. Pervasive potassic alteration and silicification overprint the wall rocks of the ore deposit. The alteration minerals include orthoclase, microcline, perthite, quartz, sericite, epidote, calcite, hematite and pyrite, with the quartz, pyrite and hematite assemblages closely associated with gold mineralization. The phases of hydrothermal alteration include: (i) potassic alteration, (ii) potassic alteration - silicification, (iii) silicification - epidotization - hematitization, (iv) silicification - sericitization - pyritization and (v) carbonation. Mass-balance calculations in potassic altered and silicified rocks reveal the gain of K2O, Na2O, SiO2, HFSEs and transition elements (TEs) and the loss of REEs. Most major elements were affected by intense mineral reactions, and the REE patterns of the ore are consistent with those of the syenites. Gold, silver and tellurium show positive correlation and close association with silicification. Fluid inclusion homogenization temperatures in quartz veins range from 154 °C to 382 °C (peak at 275 °C–325 °C), with salinities of 4–9 wt.% NaCl equiv. At temperatures of 325 °C the fluid is estimated to have pH = 3.70–5.86, log fO2 = − 32.4 to − 28.1, with Au and Te transported as Au (HS)2− and Te22 − complexes. The ore forming fluids evolved from high pH and fO2 at moderate temperatures into moderate-low pH, low fO2 and low temperature conditions. The fineness of the precipitated native gold and the contents of the oxide minerals (e.g., magnetite and hematite) decreased, followed by precipitation of Au- and Ag-bearing tellurides. The hydrothermal system was derived from an alkaline magma and the deposit is defined as an alkaline rock-hosted hydrothermal gold deposit.  相似文献   

14.
Peralkaline acid liquids: A petrological study   总被引：1，自引：0，他引：1  
Electron-microprobe analyses of the feldspars and associated ferromagnesian minerals in the peralkaline volcanics, comendites and pantellerites, are presented together with new data on the major and trace-elements of the rocks and residual glasses. The feldspar phenocrysts in the pantellerites span a narrower range (Or33–Or39) than those of the comendites (Or30–Or46); both sets show only limited increase in Or outwards, and the zoning is greatest in quartz-bearing assemblages. The feldspar microlites in the residual glasses are invariably more potassic (2–4% Or) than their associated phenocrysts. In pantellerites the feldspars become more potassic as the residual liquids become more sodic; thus the most potassic feldspar is found in the most sodic (and peralkaline) pantellerite.Of the ferromagnesian phenocrysts, aenigmatite is the most ubiquitous and is commonly associated with hedenbergite±fayalite, or ferrorichterite; in the later stages of crystallization (groundmass), it is associated with acmite, arfvedsonite and tuhualite. Aside from slight variation in Ti/Fe+Ti ratio, aenigmatite is virtually constant in composition. The pyroxenes from the different assemblages have zones which together almost span the range acmitehedenbergite. Both ferrorichterite and arfvedsonite incorporate F but not Cl, and are slightly potassic. Tuhualite exists as two varieties; one blue and potassic, the other violet and sodic; both varieties reject halogens. Using (estimated) free-energy data, a field in fo2, T space is postulated in which Fe-Ti oxides are absent; their place is taken by pyroxene and aenigmatite. The no-oxide field will be intercepted by a cooling liquid in which peralkalinity is increasing and in which fo2 is near but above the FMQ buffer.The characteristic pattern of trace-elements in peralkaline volcanics (e.g., high Nb, Ta, Zr, Mo, Zn, Cd, R.E, etc; low Sr, Ba, Mg) are considered to be as much evidence for the peralkaline (salic) condition as of the genetic process. Several lines of evidence suggest that at liquidus temperatures, peralkaline rhyolites are essentially anhydrous.  相似文献   

15.
《International Geology Review》2012,54(11):1296-1308
Geochronological, geochemical, and whole-rock Sr–Nd isotopic analyses were performed on a suite of Palaeozoic nepheline syenites from Zijinshan to characterize their ages and petrogenesis. Laser ablation inductively coupled plasma-mass spectrometry U–Pb zircon analyses yield consistent ages of 525.7 ± 2.8 million years for a sample (HYK01). These intrusive rocks belong to the foid syenite magma series in terms of K2O?+?Na2O contents (14.3–15.2 wt.%) and to the shoshonitic series based on their high K2O contents (5.42–5.61 wt.%). The nepheline syenites are further characterized by high light rare earth element contents [(La/Yb) N ?=?29.1–36.1]; show modest negative Eu anomalies (δEu?=?0.5–0.6) and positive anomalies in Rb, Th, U, Pb, Zr, and Hf; are depleted in Ba and high field strength elements (P and Ti). In addition, all the nepheline syenites in this study display relatively low radiogenic Sr (87Sr/86Sr) i (0.7042–0.7043) and positive ?Nd (t) (0.7–0.8). These results suggest that the nepheline syenites were derived from depleted continental crust. The parent magmas likely experienced fractional crystallization of plagioclase, Ti-bearing oxides (e.g. rutile, ilmenite, and titanite), apatite, and zircon during ascent, with negligible crustal contamination before final emplacement at a high crustal level.  相似文献   

16.
Nepheline natrolite syenites of Center 2 of the Coldwell alkalinecomplex exhibit rare wispy mafic-rich modal layering, extensivexenolith-rich zones and a wide variety of textural types, thelatter resulting from the imposition of high temperature shearingand recrystallization on consolidated syenite. The texturesdeveloped range from allotriomorphic granular to porphyroclasticto mosaic granulob-lastic. The nepheline syenites are pyroxene-poor.Pyroxenes occur most commonly as corroded diopside to diopsidichedenbergite cores surrounded by amphibole and less commonlyas acmitic hedenbergite overgrowths upon cores of iron-richamphiboles. Amphiboles are the dominant mafic phase and rangefrom magnesian hastingsitic hornblende to hastingsite to hastingsitichornblende to ferroedentic hornblende. Nephelines contain excesssilica and have not equilibrated to compositions characteristicof low temperatures. Feldspars lack microcline twinning andperthites and have undergone extensive ion exchange at highsub-solidus temperatutes with sodium-rich fluids. Formationof late stage primary and replacement natrolite, muscovite andthomsonite is characteristic. The nepheline syenites are consideredto be a part of a cycle of continental rift magmatism and tohave been emplaced by cauldron subsidence as a hot hydrous magma.The rocks did not undergo long term subsolidus re-equilibrationas the high temperature mineral assemblage has been preservedby uplift during post-intrusive regional block faulting. Thenepheline syenites were probably dervied by extensive fractionalcrystallization of alkali basaltic magmas.  相似文献   

17.
http://www.sciencedirect.com/science/article/pii/S1674987113000893   总被引：1，自引：0，他引：1  
Two petrologically distinct alkali feldspar syenite bodies （AFS-1 and AFS-2） from Chhotaudepur area, Deccan Large Igneous Province are reported in the present work. AFS-1 is characterized by hypidio-morphic texture and consists of feldspar （Or55Ab43 to Or25Ab71）, ferro-pargasite/ferro-pargasite horn-blende, hastingsite, pyroxene （Wo47, En5, Fs46）, magnetite and biotite. AFS-2 exhibits panidiomorphic texture with euhedral pyroxene （Wo47-50, En22-39, Fs12e31） set in a groundmass matrix of alkali feldspar （Or99Ab0.77 to Or1.33Ab98）, titanite and magnetite. In comparison to AFS-1, higher elemental concentra-tions of Ba, Sr and PREE are observed in AFS-2. The average peralkaline index of the alkali feldspar syenites is w1 indicating their alkaline nature. Variation discrimination diagrams involving major and trace elements and their ratios demonstrate that these alkali feldspar syenites have a shoshonite affinity but emplaced in a within-plate and rifting environment. No evidence of crustal contamination is perceptible in the multi-element primitive mantle normalized diagram as well as in terms of trace elemental ratios. The enrichment of incompatible elements in the alkali feldspar syenites suggests the involvement of mantle metasomatism in their genesis.  相似文献   

18.
The distribution of radioactive elements in alkaline rocks from Polar Siberia and Ukraine shows that U and Th are markedly concentrated in carbonatite complex and nepheline syenite as final products of magma fractionation. Peralkaline nepheline syenites from Polar Siberia are characterized by very high contents of radioactive elements, which are close to the economic level. Radioactive elements are also concentrated in rocks of the carbonatite complex. For example, some soevites contain up to 294 × 10?4%U and 916 × 10?4% Th. In late dolomite carbonatites, the contents of radioactive elements are appreciably lower. The Th/U ratio in alkaline rocks of Polar Siberia is close to the chondrite value in primary high-Mg rocks and increases in late derivatives: phoscorite, calcite and dolomite carbonatites. The main amount of radioactive elements is contained in rare-metal accessory minerals: perovskite, pyrochlore, calzirtite, and apatite. Rock-forming minerals are distinguished by very low concentrations of radioactive elements. In alkaline series of the Chernigovka massif (Ukraine), U and Th also accumulate in the course of crystal fractionation, especially in phoscorites from the carbonatite complex. Mantle xenoliths and alkaline rocks from Ukraine reveal uranium specialization. Most likely, the discrepancy in fractionation of radioactive elements between Polar Siberia and Ukraine is caused by different geodynamic regimes of these provinces. The Mesozoic alkaline magmatism of Polar Siberia is a part of the Siberian superplume, whereas the Proterozoic alkaline complex in Ukraine is related to subduction of the oceanic crust.  相似文献   

19.
Some 500 microprobe analyses from 43 rock samples, covering the entire range of major and minor intrusive rock-types, define the following ranges of mineral composition: plagioclases (An70-30), alkali feldspars (Or98-20 and Ab90–99), olivines (Fo85-82), clinopyroxenes (aluminous titanaugite through salite and aegirine-augite to acmite), amphiboles (subsilicic kaersutite through pargasite to hastingsite, edenite or katophorite), biotites (titanbiotite to titaniferous manganiferous lepidomelane). Varied discontinuous reaction relationships are evident petrographically between these minerals (e.g. amphibole overgrowths on pyroxenes or biotites), but most appear to reflect reequilibration during slow magmatic cooling, or perhaps local disequilibrium effects, and there is little evidence for significant subsolidus, hydrothermal or deuteric modification of the primary mineralogy.Although these mineral ranges are reasonably typical of differentiated alkaline gabbroic-syenitic intrusions, Monchique also shows many unusual features: e.g. a restricted stability range for olivine, the absence of amphiboles from all rocks with 54<%SiO2<58, a lack of alkali amphiboles corresponding to the acmite-rich pyroxenes, the presence of acmite-poor pyroxenes and aluminous biotites in peralkaline rocks, and irregular Ti variation in biotites. Mineral/ host-rock relationships also show peculiarities: e.g. Mg/ (Mg+Fe) ratios of mafic minerals and An contents of plagioclases increase as host-rock fractionation index (FI) increases from gabbroic (FI 30–40%) to alkali feldspar-bearing essexitic (FI c. 50) rocks. Thereafter, Mg ratios decrease only slightly, such that many malignites and miaskitic syenites (FI 70–90) carry pyroxenes and biotites which are no more, and sometimes less evolved than those in the gabbroic rocks (FI 30–40).Such features confirm earlier suggestions from whole-rock geochemistry, that a major evolutionary process in the complex was a relatively discontinuous segregation of already somewhat evolved essexitic magma into more basic and more felsic magmas, rather than an incremental gabbrosyenite crystal fractionation. They also confirm that the complex represents neither a single in situ differentiating magma pulse, nor a series of simply related pulses, but an irregular and largely irresolvable juxtaposition of magma-batches of widely varying compositions and evolutionary histories.  相似文献   

20.
The unaltered magmatic rocks of the Zadoi Massif were analyzed for Sr isotopic composition and concentrations of major oxides and trace elements by ICP MS. The evolution of the massif involved four phases: (i) perovskite and ilmenite clinopyroxenites, (ii) ijolites, (iii) nepheline syenites, and (iv) carbonatites. The perovskite clinopyroxenites have anomalously high Ce/Pb (223–1132) and Pr/Sr × 1000 (70–360) ratios at a low initial Sr isotopic ratio (87Sr/86Sr)0 = 0.70247–0.70285. The ilmenite clinopyroxenites have Ce/Pb and Pr/Sr × 1000 ratios approaching those in basalts of oceanic islands (OIB) (decreasing to 39 and 30, respectively) at a simultaneous increase in the (87Sr/86Sr)0 ratios (0.7030–0.7036). The ijolites and nepheline syenites have patterns of incompatible trace elements similar to those in OIB and the highest (87Sr/86Sr)0 ratios (0.70346–0.70414). The carbonatites are complementarily enriched in incompatible elements of the nepheline syenites and have (87Sr/86Sr)0 = 0.7029–0.7034, which is comparable with the range of analogous ratios for the ilmenite clinopyroxenites. Our geochemical data indicate that the carbonatites were formed as an immiscible liquid or fluid, which separated from the ijolite-nepheline syenite melt during its interaction with the source material of the perovskite and ilmenite clinopyroxenites.  相似文献   

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