五莲七宝山地区早白垩世碱性侵入岩成因及其地质意义

山东五莲七宝山地区早白垩世的碱性侵入岩位于火山机构的中央部位,该岩体具有高Ba-Sr含量、高Nb/Ta和Zr/Hf比、低Ti/Eu比等特征,前人的研究指出其起源于岩石圈地幔。然而,该侵入体中的岩性与成分变化所反映的深部动力学过程尚未理清。本文对七宝山二长辉长岩和两类辉石二长岩开展了详细的矿物学和岩石地球化学研究,识别出钠质和钾质两类钾玄质岩石系列。该套碱性中基性侵入岩具有富碱、富轻稀土和富大离子亲石元素的特征,同时具有高的(La/Yb)_N和(Gd/Yb)_N值。碱性侵入岩中两类单斜辉石和两类斜长石作为再循环晶,记录了不同批次岩浆/熔体的混合,这些矿物组分和全岩成分共同约束了岩浆的起源与演化过程。结合前人的地球化学资料,本文指出七宝山碱性侵入岩的源区是曾受到沉积物交代的富集地幔,源区存在金云母脉体和角闪石脉体。上述脉体连同周围的地幔橄榄岩共同发生部分熔融,形成原生的碱性熔体。七宝山碱性侵入岩显示高的Nb/Ta和Zr/Hf比、低的Ti/Eu比,同时在微量元素蜘蛛图上呈现Ti^*和Hf^*的负异常,结合高稀土单斜辉石平衡熔体的属性,共同指示了碳酸盐熔体组分对该套碱性侵入岩的形成发挥了重要作用。钠质系列与钾质系列岩石反映了源区富碱矿物相类型相对贡献量的差异,即钠质为主的碱性岩反映源区角闪石的贡献更大,而钾质为主的碱性岩反映源区金云母的贡献占优势。此外,碱性侵入岩中的钾质系列具有异常高的Rb-Zr-Hf-U含量,很可能反映了源区在部分熔融过程中热液锆石熔解后形成的熔体加入到了钾质岩浆房内。本研究强调了碳酸盐熔体组分对高Nb/Ta碱性中基性的形成发挥着重要作用,亦强调了热液锆石的熔解加入导致岩浆具有高Zr-Hf-U含量的特征。     

Petrogenesis of alkaline rocks from Murud-Janjira, in the Deccan Traps, Western India

A late-stage rift-related tholeiite-alkalic suite of igneous intrusions cut the Deccan Traps lavas at the western Indian continental margin. The suite comprises intrusives that can be grouped into ten lithotypes on the basis of their mutual relationships. Tholeiitic types predate the alkaline rocks and greatly predominate, however, the alkaline members exhibit more diversity in mineralogy and chemistry, and are amongst the rare magmatic rocks from the Deccan that host both mantle and lower crustal xenoliths. The mineralogy of most rock types is dominated by clinopyroxene. The diversity of the alkaline rocks could be mainly accounted for by fractional crystallization and mixing between evolved and primitive melts under varying P-T conditions. Sodic and potassic lamprophyres are amongst the most primitive samples with high Mg #, FeO/MgO < 1, high Cr and also with relatively high Ba, Sr, Zr and Nb. They are the most deeply derived magmas within the Deccan Traps as is evident from the mantle and lower crustal xenoliths entrained by them. They possibly represent low degree melts of incompatible element-enriched mantle source rocks. The nephelinites are strongly porphyritic and despite their high Mg #s can be regarded as evolved magmas that have been responsible for the formation of the tephriphonolite daughter. The nephelinites have undergone contamination by lower crustal granulites. The composite intrusions of microdiorites with their complexly zoned mineralogy dominated by plagioclase and amphiboles/micas represent hybrid rocks that have resulted from mixing between tholeiitic and trachytic melts partly at depth and partly at shallow crustal levels.     

Geochemistry and geochronology of mafic rocks from Bamenda Mountains (Cameroon): Source composition and crustal contamination along the Cameroon Volcanic Line

Mafic rocks from the Bamenda volcanic province along the Cameroon Volcanic Line have been dated from 17 to 0 Ma. Associated with some trachytes and rhyolites, this volcanism covers a period of more than 25 Ma. The studied rocks are basalts to mugearites. Most of them have been contaminated by continental crust during their transit to the surface. The oldest rocks are the most contaminated. One group of samples shows high Eu, Sr and Ba contents. This characteristic is not due to crustal contamination process, but has a mantle source origin. We argue that these characteristics have been acquired by mixing of melts formed by partial melting of mantle pyroxenites with melts formed in mantle peridotites. Such pyroxenites have been observed as mantle xenoliths in the Adamaoua province, and their chemical and isotopic compositions are consistent with such a model.     

Geochemistry of Miocene trachytes in Bugasi, Lhasa block, Tibetan Plateau: Mixing products between mantle- and crust-derived melts?

It is generally believed that Cenozoic potassic and ultrapotassic volcanic rocks of the Tibetan Plateau were generated by partial melting of an enriched mantle region or lower crustal materials. The Miocene Bugasi volcanic rocks (BVR) in the western part of the Lhasa block are composed mainly of trachyandesites and trachytes, both of which belong to the shoshonite series. The trachytes show somewhat transitional compositions between the mantle-derived trachyandesites of the BVR and the crust-derived potassic rocks of Konglongxiang, most evident in their Sr, Ba, and Ni concentrations, Nb/Ta, Rb/Sr, Th/Nb, Zr/Nb, and Ba/Rb trace element ratios, and Sr and Nd isotopic compositions. These features, coupled with the relatively high Cr and Ni concentrations and Mg#, suggest that the trachytes are the product of mixing between mantle-derived and lower crust-derived melts.     

Geochemical and isotopic investigation of the Laiwu–Zibo carbonatites from western Shandong Province, China, and implications for their petrogenesis and enriched mantle source

Major and trace element and Nd–Sr isotope data of the Mesozoic Laiwu–Zibo carbonatites (LZCs) from western Shandong Province, China, provide clues to the petrogenesis and the nature of their mantle source. The Laiwu–Zibo carbonatites can be petrologically classified as calcio-, magnesio- and ferro-carbonatites. All these carbonatites show a similarity in geochemistry. On the one hand, they are extremely enriched in Ba, Sr and LREE and markedly low in K, Rb and Ti, which are similar to those global carbonatites, on the other hand, they have extremely high initial ⁸⁷Sr/⁸⁶Sr (0.7095–0.7106) and very low _Nd (−18.2 to −14.3), a character completely different from those global carbonatites. The small variations in Sr and Nd isotopic ratios suggest that crustal contamination can not modify the primary isotopic compositions of LZC magmas and those values are representatives of their mantle source. The Nd–Sr isotopic compositions of LZCs and their similarity to those of Mesozoic Fangcheng basalts imply that they derived from an enriched lithospheric mantle. The formation of such enriched lithospheric mantle is connected with the major collision between the North China Craton (NCC) and the Yangtze Craton. Crustal materials from the Yangtze Craton were subducted beneath the NCC and melts derived from the subducted crust of the Yangtze Craton produced an enriched Mesozoic mantle, which is the source for the LZCs and Fangcheng basalts. The absence of alkaline silicate rocks, which are usually associated with carbonatites suggest that the LZCs originated from the mantle by directly partial melting.     

Trace elements in minerals as indicators of the evolution of alkaline ultrabasic dike series: LA-ICP-MS data for the magmatic provinces of northeastern Fennoscandia and Germany

In this paper we report the results of the analysis of rare earth (REE), large-ion lithophile (LILE), and high field strength (HFSE) elements in minerals from the alkaline lamprophyre dikes of the Kola region and the Kaiserstuhl province by the local method of laser ablation inductively coupled plasma mass spectrometry. The contents of Y, Li, Rb, Ba, Th, U, Ta, Nb, Sr, Hf, Zr, Pb, Be, Sc, V, Cr, Ni, Co, Cu, Zn, Ga, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu were measured in olivine, melilite, clinopyroxene, amphibole, phlogopite, nepheline, apatite, perovskite, and the host fine-grained groundmass. The obtained data on trace element partitioning among the mineral phases of the alkaline ultrabasic rocks of the dike series indicate that the main mineral hosts for the HFSEs and REEs in alkaline picrites, olivine melanephelinites, and melilitites are perovskite and apatite comprising more than 90% of these elements. Among major rock-forming minerals, melilite, clinopyroxene, and highly magnesian amphibole make a significant contribution to the balance of REEs during the evolution of melanephelinite melts. The partition coefficients of Ni, Co, Cu, Zn, Sc, V, Cr, Ga, Y, Li, Rb, Ba, Th, U, Ta, Nb, Sr, Hf, Zr, Pb, Be, and all of the REEs were calculated for olivine, clinopyroxene, amphibole, phlogopite, nepheline, perovskite, and apatite on the basis of mineral/groundmass ratios. Variations in the composition of complex zoned clinopyroxene phenocrysts reflect the conditions of polybaric crystallization of melanephelinite melt, which began when the magmas arrived at the base of the lower crust and continued during the whole period of their ascent to the surface. The formation of green cores in clinopyroxene is an indicator of mixing between primary melanephelinite melts and phonolite magmas under upper mantle conditions. The estimation of the composition of primary melts for the rocks of the alkaline ultrabasic series of the Kola province indicated a single primary magma for the whole series. This magma produced pyroxene cumulates and complementary melilitolites, foidolites, and nepheline syenites.     

西天山托云盆地及周边中新生代岩浆活动的岩石学、地球化学与年代学研究

天山西南部白垩纪-老第三纪发育的托云盆地及其周边出露的岩浆岩是一套完整的碱性岩浆岩系列，包含了苦橄质玄武岩、玄武岩、碧玄岩、碱玄岩（橄榄玄武岩、黑云母辉长二长岩、辉长辉绿岩、辉石橄榄岩）和响岩等多种岩石类型。野外工作显示有火山喷出岩和侵入岩两种不同的产状。年代学结果指示岩浆岩形成于120-50Ma间，为晚白垩世-老第三纪盆地形成演化阶段岩浆活动的产物。分离结晶作用是岩浆演化和岩浆系列形成最主要的因素，托云岩浆岩大致经历了结晶分异过程的两个阶段：早期苦橄质岩浆中橄榄石、尖晶石的结晶分离，表现为MgO和微量元素Cr含量随SiO2含量增加大幅度的降低；晚期主要是单斜辉石、斜长石和钛铁矿等矿物的结晶分异，以CaO、FeO、TiO2等随SiO2含量增加大幅度的降低为特点。苦橄质岩石的出现指示了地幔较高温熔融事件的存在，进而为托云盆地地幔柱的存在提供了有力的证据。无论如何，碱性岩浆的活动表明托云盆地形成的大地构造背景是大陆主动裂谷环境，对应的深部背景为区域性的地幔柱构造。首次发现的响岩是结晶分异作用的最终产物。响岩较极端地指示了岩浆结晶分离过程对岩浆演化的巨大影响。托云岩浆岩的同位素特征指示其源区是一个接近于PREMA地幔，但微量元素特征显示其受地壳流体交代改造的特点。岩浆岩的Nd同位素TDM集中在250～600Ma之间，反映了一个古生代时期形成的新生岩石圈地幔，与新疆北部地区的晚古生代新生岩石圈地幔的事实相符。     

Metasomatic events recorded in ultramafic xenoliths from the Hyblean area (Southeastern Sicily, Italy)

Three types of ultramafic xenoliths from the Hyblean area (Sicily) show prime evidence for mantle metasomatism, namely: 1) Spinel-facies depleted harzburgite veined by phlogopite-bearing clinopyroxenite; 2) Amphibole-bearing harzburgite; and 3) Al-spinel websterite. (2) and (3) exhibit glassy pockets having respectively mugearitic and basanitic compositions, but a little amount of glass with low Ca and very low alkalis in (2). Glasses generally show trace element distributions consistent with the partial melting of pargasite-dominated mineral assemblages. Abundant Ca-Mg-carbonate globules immersed in these glassy pockets testify to immiscibility between silicate and carbonatite melts. Silicate melts and hydrous-silicate supercritical fluids, which underwent phase separation during fluxing throughout the semi-brittle lithospheric mantle, may account for such metasomatizing processes. The nature and abundance of some fluid-mobile elements in glasses and hydrous minerals (especially the Ca-poor glass, with B?=?59 ppm, Li?=?27 ppm, Ba?=?700 ppm and phlogopite, with Ba?=?8,465 ppm, Sr?=?260 ppm, F?=?5,700 ppm) suggest that some hydrous fluids may derive from hydrothermally altered oceanic crust. Conversely, metasomatizing silicate melts probably have a deep-seated origin. These results confirm previous suggestions on the key role of mantle metasomatism in the origin of some alkaline Hyblean magmas.     

Mathiasite-loveringite and priderite in mantle xenoliths from the Alto Paranaíba Igneous Province,Brazil: genesis and constraints on mantle metasomatism

Alkali-bearing Ti oxides were identified in mantle xenoliths enclosed in kimberlite-like rocks from Limeira 1 alkaline intrusion from the Alto Paranaíba Igneous Province, southeastern Brazil. The metasomatic mineral assemblages include mathiasite-loveringite and priderite associated with clinopyroxene, phlogopite, ilmenite and rutile. Mathiasite-loveringite (55–60 wt.% TiO₂; 5.2–6.7 wt.% ZrO₂) occurs in peridotite xenoliths rimming chromite (～50 wt.% Cr₂O₃) and subordinate ilmenite (12–13.4 wt.% MgO) in double reaction rim coronas. Priderite (Ba/(K+Ba)< 0.05) occurs in phlogopite-rich xenoliths as lamellae within Mg-ilmenite (8.4–9.8 wt.% MgO) or as intergrowths in rutile crystals that may be included in sagenitic phlogopite. Mathiasite-loveringite was formed by reaction of peridotite primary minerals with alkaline melts. The priderite was formed by reaction of peridotite minerals with ultrapotassic melts. Disequilibrium textures and chemical zoning of associated minerals suggest that the metasomatic reactions responsible for the formation of the alkali-bearing Ti oxides took place shortly prior the entrainment of the xenoliths in the host magma, and is not connected to old (Proterozoic) mantle enrichment events.     

云南祥云马厂箐富碱斑岩体的地球化学特征及其形成的构造环境

云南祥云马厂箐岩体处于扬子板块西缘与NW向的金沙江—哀牢山深大断裂带东侧交汇部位,属于哀牢山—金沙江富碱侵入岩带的组成部分。马厂箐岩体主要为花岗斑岩、二长斑岩和正长斑岩,岩体化学成分具有富碱、富铝和高钾的特点。岩石富集大离子亲石元素(Rb、Sr、Ba、Th和U)和轻稀土元素(LREE)、相对亏损高场强元素(Ta、Nb和Ti),且Ta、Nb和Ti具"TNT"负异常;LREE/HREE值为8.04～23.99,δEu值为0.72～0.88,负Eu异常不明显;n(87Sr)/n(86Sr)值范围为0.7072～0.7086,均值为0.7080,高于原始地幔现代值0.7045;n(143Nd)/n(144Nd)值范围为0.5121～0.5124,均值0.5123,低于原始地幔现代值0.512638;ISr值范围为0.7061～0.7075,均值为0.7070;εNd值范围为(3.1～(10.2,均值为(6.8。马厂箐岩体既不属于传统的含碱性暗色矿物的碱性岩类,也不同于典型的A型花岗岩,应属于富碱侵入岩类;岩体的岩浆起源于壳—幔物质混合的一种所谓EMⅡ型富集地幔源;其壳幔混合特征,主要是俯冲进入上地幔的地壳物质与地幔物质发生了源区混合作用的结果;形成于碰撞后的板内构造环境。     

Sources and geodynamic setting of petrogenesis of the Middle Cambrian Upper Petropavlovka alkaline basic pluton (Kuznetsk Alatau,Siberia)

Early Paleozoic alkaline basic magmatism in the Kuznetsk Alatau is manifested in the Upper Petropavlovka pluton of gabbro, feldspathoid rocks (theralites, mafic foidolites, and nepheline syenites), and Ca-carbonatites. According to Sm–Nd and Rb–Sr isotope data, the pluton formed in the Middle Cambrian (509 ± 10 Ma). The silicate igneous rocks correspond in the contents of silica, alumina, and alkalies to derivates of a K–Na alkaline basic association. The Ca-carbonatites are characterized by a high-temperature (600–900 °C) paragenesis of apatite, clinopyroxene, ferromonticellite, phlogopite, and magnetite. They are enriched in P2O5 (up to 6.4 wt.%), Sr (up to 3000–4500 ppm; Sr/Ba ~ 5–7), and REE + Y (up to 800 ppm) and show evidence for liquation genesis. The predominant magmatic source (εNd(T) = 5–7) was moderately depleted PREMA, possibly combined with E-MORB and EM. According to the isotopic data ((87Sr/86Sr)T ~ 0.7024–0.7065; δ18O ~ 6.3–15.5‰; δ18C ~ –3.5 to –2.0‰), the fractionation of the melts was accompanied by their crustal contamination. The trace-element composition of the mafic rocks testifies to the participation of a substance similar to the substrata of the parental magmas of MORB, IAB, and OIB in the magma generation. This suggests intrusion in the geodynamic setting of interaction between the active continental margin and an ascending mantle diapir. Most likely, the intrusion led to the mixing of material from different sources, including the components of PREMA, enriched suprasubduction lithospheric mantle (EM), and continental crust. The assumption is made that the complexes of highly alkaline rocks and carbonatites in the western Central Asian Fold Belt are of plume origin and belong to an Early Paleozoic large igneous province.     

Isotopic evidence for genetic relations between acid and alkaline rocks in Italy

Pb isotopic composition and concentrations were determined for whole-rock samples from the Pliocene-Pleistocene, acid, Tuscan Igneous Province, Italy, in order to clarify their relation to the Cenozoic alkaline volcanism of Central Italy. The Pb of the Tuscan rocks is fairly uniform in its isotopic composition, despite variable and high ₈₇Sr/₈₆Sr ratios (0.711–0.725; Barberi et al, 1971).A comparison of the Pb isotopic composition in the Tuscan and the potassic alkaline rocks strongly suggests a continuous mixing relation between both rock series, with partial melts of mantle material and argillaceous sedimentary rocks as likely end-members. Such an interrelation could also provide a simple explanation for the range in the Sr isotopic ratio within the Tuscan rocks. The favoured model envisages a similar history for both rock-series; it is suggested that their main petrographic differences result from a lower portion of mantle-derived material in the parental material for the Tuscan rocks, and from the mineral phases present in the residue during partial melting of the source region.     

The main geochemical features of carbonatites

A great deal of data is available on the geochemistry of the carbonatite family as well as diverse sedimentary, metamorphic and endogenic carbonate rocks. The distinctive geochemical features of carbonatites are expressed first of all in their simultaneous enrichment in Sr, Ba, ree and V. Since the carbonatite family is related both to alkaline petrogenesis and a mantle origin, these associations allow distinction of carbonatites from the large variety of other carbonate rocks. At the same time, carbonatites associated with different types of alkaline rocks under different geologic-tectonic settings differ in contents of a number of elements (Sr, Ba, Nb, ree, Pb, Zn, P). These differences permit the geochemical classification of various rock associations of carbonatites. This geochemical classification is of practical interest because the ore productivity of the various associations is different.     

New data on carbonatites of the Il’mensky-Vishnevogorsky alkaline complex,the southern Urals,Russia

Carbonatites that are hosted in metamorphosed ultramafic massifs in the roof of miaskite intrusions of the Il’mensky-Vishnevogorsky alkaline complex are considered. Carbonatites have been revealed in the Buldym, Khaldikha, Spirikha, and Kagan massifs. The geological setting, structure of carbonatite bodies, distribution of accessory rare-metal mineralization, typomorphism of rock-forming minerals, geochemistry, and Sr and Nd isotopic compositions are discussed. Dolomite-calcite carbonatites hosted in ultramafic rocks contain tetraferriphlogopite, richterite, accessory zircon, apatite, magnetite, ilmenite, pyrrhotite, pyrite, and pyrochlore. According to geothermometric data and the composition of rock-forming minerals, the dolomite-calcite carbonatites were formed under K-feldspar-calcite, albite-calcite, and amphibole-dolomite-calcite facies conditions at 575–300°C. The Buldym pyrochlore deposit is related to carbonatites of these facies. In addition, dolomite carbonatites with accessory Nb and REE mineralization (monazite, aeschynite, allanite, REE-pyrochlore, and columbite) are hosted in ultramafic massifs. The dolomite carbonatites were formed under chlorite-sericite-ankerite facies conditions at 300–200°C. The Spirikha REE deposit is related to dolomite carbonatite and alkaline metasomatic rocks. It has been established that carbonatites hosted in ultramafic rocks are characterized by high Sr, Ba, and LREE contents and variable Nb, Zr, Ti, V, and Th contents similar to the geochemical attributes of calcio-and magnesiocarbonatites. The low initial ⁸⁷Sr/⁸⁶Sr = 0.7044?0.7045 and εNd ranging from 0.65 to ?3.3 testify to their derivation from a deep mantle source of EM₁ type.     

Ultrapotassic Volcanism of the Valagin Ridge,Kamchatka

New isotopic-geochemical data are reported on the Late Cretaceous–Paleocene ultrapotassic volcanic rocks of the alkaline–ultrabasic complex of the Valagin Ridge, Eastern Kamchatka. The high Mg, low Ca and Al contents at high K/Na ratios in these rocks make them similar to the Mediterranean-type lamproites and ultrapotassic rocks. The low contents of high-field strength (HFSE) and heavy rare-earth (HREE) elements relative to the MORB composition, and the low Sr and high Nd isotopic ratios indicate the formation of their primary melts from a depleted mantle source. The enrichment of the ultrapotassic rocks in the large-ion lithophile elements (LILE) can be explained by the fluid influx in melts during melting of subsided oceanic crust.     

Petrogeochemistry and genesis of listwaenite xenoliths in the alkali basalts of the southern Tien Shan

Mesozoic alkaline (subalkaline) mafic rocks from the southern Tien Shan contain numerous listwaenite xenoliths (on average, 50–60% of all xenoliths) and less abundant serpentinites, which develop after nodules of mantle spinel lherzolites and, more rarely, pyroxenites. Various models of listwaenite genesis and the problem of a “listwaenite layer” were considered. The listwaenites consist of three heterogeneous mineral (element) assemblages of different ages: (a) mantle ultrabasic protolith (relics of spinels, pyroxenes, and other minerals); (b) products of shallow-depth serpentinization; and (c) minerals (elements) of hydrothermal-metasomatic carbonation (listwaenitization), which occurred under near-surface conditions but was related to mantle fluids (carbon isotope signatures of carbonates, introduction of Sr, its correlation with CO₂, etc.). It cannot be ruled out that the CO₂ degassing of the mantle occurred not only in the Mesozoic but also in the Cenozoic. This process was accompanied by the formation of occurrences of chalcophile elements (Hg, Sb, Au, Ag, Zn, Cu, and Pb), F, Ba, and Sr. Late Cenozoic celestite deposits deserve special attention in this context. They form the largest Sr province in the Mediterranean mobile belt and were presumably also related to mantle sources.     

Plume-related mantle source of super-large rare metal deposits from the Lovozero and Khibina massifs on the Kola Peninsula, Eastern part of Baltic Shield: Sr, Nd and Hf isotope systematics

The two world’s largest complexes of highly alkaline nepheline syenites and related rare metal loparite and eudialyte deposits, the Khibina and Lovozero massifs, occur in the central part of the Kola Peninsula. We measured for the first time in situ the trace element concentrations and the Sr, Nd and Hf isotope ratios by LA-ICP-MS (laser ablation inductively coupled plasma mass spectrometer) in loparite, eudialyte an in some other pegmatitic minerals. The results are in aggreement with the whole rock Sr and Nd isotope which suggests the formation of these superlarge rare metal deposits in a magmatic closed system. The initial Hf, Sr, Nd isotope ratios are similar to the isotopic signatures of OIB indicating depleted mantle as a source. This leads to the suggestion that the origin of these gigantic alkaline intrusions is connected to a deep seated mantle source—possibly to a lower mantle plume. The required combination of a depleted mantle and high rare metal enrichment in the source can be explained by the input of incompatible elements by metasomatising melts/fluids into the zones of alkaline magma generation shortly before the partial melting event (to avoid ingrowth of radiogenic isotopes). The minerals belovite and pyrochlore from the pegmatites are abnormally high in ⁸⁷Sr /⁸⁶Sr ratios. This may be explained by closed system isotope evolution as a result of a significant increase in Rb/Sr during the evolution of the peralkaline magma.     

Trace element geochemistry of phlogopite-rich mafic mantle xenoliths: their classification and their relationship to phlogopite-bearing peridotites and kimberlites revisited

Kimberlite magmas from the Kimberley area of South Africa have sampled two main types of phlogopite-rich mafic xenoliths which represent deep mantle segregations from highly alkaline melts. The first group corresponds to the MARID rocks characterised by the mineral association mica (phlogopite)-amphibole (K-richterite)-rutile-ilmenite-clinopyroxene and the second group consists of the PIC rocks characterised by the mineral association mica (phlogopite)-ilmenite-clinopyroxene-minor rutile. The two groups are clearly distinguished from one another by their mineral paragenesis, by the major element composition of their phlogopite and ilmenite, by the trace element content of their clinopyroxene and by their clinopyroxene and whole rock Sr and Nd isotope ratios. The combined major and trace element variations are interpreted to indicate a genetic relationship between the PIC rocks and group I kimberlite magma, and between the MARID rocks and group II kimberlite magma. The two types of parental melts percolated through, and metasomatised, the upper mantle beneath the Kimberley area as indicated by the trace element characteristics of the clinopyroxenes of the studied phlogopite-bearing peridotites.     

Sm-Nd and Rb-Sr isotopic systems and captured He and hydrocarbon gases as markers of melt sources and fluid regime under which the oceanic crust of the Mid-Atlantic Ridge was formed at 5°–6° N

The paper presents characteristics of the Nd and Sr isotopic systems of ultrabasic rocks, gabbroids, plagiogranites, and their minerals and data on He and hydrocarbons in fluid inclusions in the same samples. The materials presented in this publication were obtained by studying samples dredged from the MAR crest zone at 5°–6° N (U/Pb zircon dating, geochemical and petrological-mineralogical studies). It was demonstrated that the variations in the isotopic composition of He entrapped in the rocks and minerals were controlled by variable degrees of mixing of juvenile He, which is typical of basaltic glass of MAR (DM source) and atmospheric He. An increase in the fraction of atmospheric He in the plutonic rocks and, to a lesser degree, in their minerals reflects the involvement of seawater or the hydrated material of the oceanic crust in the magmatic and postmagmatic processes. This conclusion finds further support in a positive correlation between the fraction of mantle He (R) and the ⁸⁷Sr/⁸⁶Sr ratio. The high-temperature hydration of ultrabasic rocks (amphibolization) was associated with an increase in the fraction of mantle He, while their low-temperature hydration (serpentinization) was accompanied by a drastic decrease in this fraction and a significant increase in the ⁸⁷Sr/⁸⁶Sr ratio. The insignificant variations in the ¹⁴³Nd/¹⁴⁴Nd (close to 0.5130) and ⁸⁷Sr/⁸⁶Sr (0.7035) in most of the gabbroids and plagiogranites, as well as the fraction of mantle He in these rocks, amphibolites, and their ore minerals, indicate that the melts were derived from the depleted mantle. Similar?_Nd values of the gabbroids, plagiogranites, and fresh harzburgites (6.77–8.39) suggest that these rocks were genetically related to a single mantle source. The value of ?_Nd = 2.62 of the serpentinized lherzolites likely reflects relations of these relatively weakly depleted mantle residues to another source. The aforementioned characteristics of the rocks generally reflect the various degrees of mixing of components of the depleted mantle with crustal components (seawater) during the metamorphic and hydrothermal processes that accompanied the formation of the oceanic crust.     

新疆准噶尔北缘北塔山组火山岩年龄及岩石成因

对准噶尔北缘北塔山组辉石玄武岩进行了LA-ICP-MS锆石U-Pb 年龄测定, 获得了玄武岩的喷发年龄380.5±2.2Ma,表明北塔山组火山岩形成于中泥盆世。该地层火山岩中辉石玄武岩和无斑玄武岩的SiO₂含量为47.55%~52.97%、Al₂O₃的含量为8.44%~20.00%、TiO₂为0.5%~1.2%,MgO含量为2.8%~15.35%、CaO为3.98%~14.83%、FeO^T为9.46%~19.23%,具有亚碱性拉斑玄武岩的特征。其微量元素显示富集大离子亲石元素(LILE)和轻稀土元素(LREE),亏损Nb、Ta和Ti,Eu异常不明显。它们具有极低的初始⁸⁷Sr/⁸⁶Sr同位素比值(0.703835~0.704337)和高的ε_Nd(381Ma)值(+6.84~+12.3,t=381Ma)的亏损地幔源区特征。结合区域地质背景,北塔山组火山岩形成于与俯冲作用相关的构造环境,是准噶尔古洋盆于泥盆世时发生的俯冲-消减所引发的岛弧岩浆作用的地质记录。岩浆源区为被流体或沉积物熔体交代改造的地幔楔和软流圈地幔,不同类型的岩石系不同成分的原始岩浆经不同演化过程的产物。