Petrology of basalts from the Mohns-Knipovich Ridge; the Norwegian-Greenland Sea

Major element compositions of submarine basalts, quenched glasses, and contained phenocrysts are reported for samples from 25 dredge stations along the Mohns-Knipovich Ridge between the Jan Mayen fracture zone and 77°30N. Most of the basalts collected on the Jan Mayen platform have a subaerial appearance, are nepheline normative, rich in incompatible elements, and have REE-patterns strongly enriched in light-REE. The other basalts (with one exception) are tholeiitic pillow basalts, many of which have fresh quenched glass rims. From the Jan Mayen platform northeastwards the phenocryst assemblage changes from olivine±plagioclase±clinopyroxene±magnetite to olivine +plagioclase±chrome-spinel. This change is accompanied by a progressive decrease in the content of incompatible elements, light-REE enrichments and elevation of the ridge that are similar to those observed south of the Azores and Iceland hotspots. Pillow basalts and glasses collected along the esternmost part of the Mohns Ridge (450 to 675 km east of Jan Mayen) have low K₂O, TiO₂, and P₂O₅ contents, light-REE depleted patterns relative to chondrites, and Mg/(Mg+Fe²⁺) ratios between 0.64 and 0.60. Pillow basalts and glasses from the Knipovich Ridge have similar (Mg/Mg+Fe²⁺) ratios, but along the entire ridge have slightly higher concentrations of incompatible elements and chondritic to slightly light-REE enriched patterns. The incompatible element enrichment increases slightly northward. Plagioclase phenocrysts show normal and reverse zoning on all parts of the ridge whereas olivines are unzoned or show only weak normal zoning. Olivine-liquid equilibrium temperatures are calculated to be in the range of 1,060–1,206° C with a mean around 1,180° C.Rocks and glasses collected on the Jan Mayen Platform are compositionally similar to Jan Mayen volcanic products, suggesting that off-ridge alkali volcanism on the Jan Mayen Platform is more widespread than so far suspected. There is also evidence to suggest that the alkali basalts from the Jan Mayen Platform are derived from deeper levels and by smaller degrees of partial melting of a mantle significantly more enriched in light-REE and other incompatible elements than are the tholeiitic basalts from the Eastern Mohns and Knipovich Ridge. The possibility of the presence of another hitherto unsuspected enriched mantle region north of 77° 30 N is also briefly considered.It remains uncertain whether geochemical gradients revealed in this study reflect: (1) the dynamics of mixing during mantle advection and magma emplacement into the crust along the Mid-Atlantic Ridge (MAR) spreading axis, (e.g. such as in the mantle plume — large-ion-lithophile element depleted asthenosphere mixing model previously proposed); or (2) a horizontal gradation of the mantle beneath the MAR axis similar to that observed in the overlying crust; or (3) a vertical gradation of the mantle in incompatible elements with their contents increasing with depth and derivations of melts from progressively greater depth towards the Jan Mayen Platform.     

Geochemistry and mineralogy of lavas from the Arakapas Fault Belt,Cyprus: Consequences for magma chamber evolution

Résumé Résumé L'étude géochimique des laves dans la zone d'Arakapas (AFB) a permis de proposer un modèle génétique pour la formation des laves et des cumulats qui s'est déroulée dans un seul site géotectonique. Cinq types de lave ont été définis dans l'AFB, un dans la séquence axiale (AS) et quatre dans les laves en coussin supérieures (UPL) formés à partir d'un manteau très déprimé dont le degré d'appauvrissement s'est accru avec le temps. La modélisation des processus de fusion partielle et de cristallisation fractionnée implique des coefficients de partage élevés pour Mg et Cr et faibles pour V compatibles avec une fugacité d'oxygène élevée dans la source.Dans les différents types de lave, la cristallisation plus ou moins précoce du plagioclase, du clinopyroxène ou de l'orthopyroxène après l'olivine témoigne de l'existence de magmas parentaux distincts qui ont alimenté des chambres magmatiques évoluant en système fermé. La disparition des grandes chambres magmatiques d'où ont été issues les laves de type A a eu lieu en fin de formation de l'AS. Les chambres magmatiques plus petites liées aux UPL ont été détruites à différents stades de leur évolution.

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Geochemistry and mineralogy of lavas from the Arakapas Fault Belt, Cyprus: Consequences for magma chamber evolution

Summary The results of geochemical investigations in the Arakapas Fault Belt (AFB) in the Cyprus ophiolite are discussed to provide a comprehensive model for the genesis of the ophiolitic intrusive and extrusive rocks which occur in a single but evolutive tectonic environment.On the basis of field and petrographic criteria, five lava types are defined, one in the Axis Sequence (AS) and four in the Upper Pillow Lavas (UPL). The comparison between observed and calculated partial melting and fractional crystallization trends favors high D_Cr and D_Mg and low Dv consistent with high fO₂. Partial melting occurred in a depleted mantle after a prior melting event. The extent of mantle depletion varies with space and increases with time.Different crystallization orders in lavas reflect distinct parental magma compositions and the extent of pre-eruption fractionation dominated by wehrlitic crystallization in closed magma chambers. Long-lived magma chambers disappear at the end of the AS. Small magma chambers occurred during the formation of the UPI, and were destroyed at various degrees of evolution.

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With 6 Figures     

Seismicity of the Norwegian Sea: The Jan Mayen Fracture Zone

The seismicity of the Jan Mayen Island region is re-examined, and a new and improved seismicity map is presented. These data, together with four previously published and one new and very precise fault-plane solution, have been interpreted in the light of other geophysical information bearing on the area. The data support the hypothesis that the transform portion of the Jan Mayen Fracture Zone consists of a system of en-échelon faults. A separate seismicity area immediately northeast of the Jan Mayen Island itself is quite pronounced on the new seismicity map. Moreover, from the available earthquake data the suggested Iceland—Jan Mayen ridge offset is located at 70.75°N.     

Mineral chemistry of submarine lavas from Hilo Ridge, Hawaii: implications for magmatic processes within Hawaiian rift zones

The crustal history of volcanic rocks can be inferred from the mineralogy and compositions of their phenocrysts which record episodes of magma mixing as well as the pressures and temperatures when magmas cooled. Submarine lavas erupted on the Hilo Ridge, a rift zone directly east of Mauna Kea volcano, contain olivine, plagioclase, augite ±orthopyroxene phenocrysts. The compositions of these phenocryst phases provide constraints on the magmatic processes beneath Hawaiian rift zones. In these samples, olivine phenocrysts are normally zoned with homogeneous cores ranging from ∼ Fo₈₁ to Fo₉₁. In contrast, plagioclase, augite and orthopyroxene phenocrysts display more than one episode of reverse zoning. Within each sample, plagioclase, augite and orthopyroxene phenocrysts have similar zoning profiles. However, there are significant differences between samples. In three samples these phases exhibit large compositional contrasts, e.g., Mg# [100 × Mg/(Mg+Fe⁺²)] of augite varies from 71 in cores to 82 in rims. Some submarine lavas from the Puna Ridge (Kilauea volcano) contain phenocrysts with similar reverse zonation. The compositional variations of these phenocrysts can be explained by mixing of a multiphase (plagioclase, augite and orthopyroxene) saturated, evolved magma with more mafic magma saturated only with olivine. The differences in the compositional ranges of plagioclase, augite and orthopyroxene crystals between samples indicate that these samples were derived from isolated magma chambers which had undergone distinct fractionation and mixing histories. The samples containing plagioclase and pyroxene with small compositional variations reflect magmas that were buffered near the olivine + melt ⇒Low-Ca pyroxene + augite + plagioclase reaction point by frequent intrusions of mafic olivine-bearing magmas. Samples containing plagioclase and pyroxene phenocrysts with large compositional ranges reflect magmas that evolved beyond this reaction point when there was no replenishment with olivine-saturated magma. Two of these samples contain augite cores with Mg# of ∼71, corresponding to Mg# of 36–40 in equilibrium melts, and augite in another sample has Mg# of 63–65 which is in equilibrium with a very evolved melt with a Mg# of ∼30. Such highly evolved magmas also exist beneath the Puna Ridge of Kilauea volcano. They are rarely erupted during the shield building stage, but may commonly form in ephemeral magma pockets in the rift zones. The compositions of clinopyroxene phenocryst rims and associated glass rinds indicate that most of the samples were last equilibrated at 2–3 kbar and 1130–1160 °C. However, in one sample, augite and glass rind compositions reflect crystallization at higher pressures (4–5 kbar). This sample provides evidence for magma mixing at relatively high pressures and perhaps transport of magma from the summit conduits to the rift zone along the oceanic crust-mantle boundary. Received: 8 July 1998 / Accepted: 2 January 1999     

Geochemistry and petrology of lavas from the submarine flanks of Réunion Island (western Indian Ocean): implications for magma genesis and the mantle source

Summary Major and trace element data as well as Sr and Nd isotope compositions for submarine lavas from the flanks of Réunion island are reported. The submarine basalts of the island have major and trace element compositions similar to those of the subaerial basaltic rocks. This implies that no compositional change occurs in the shield-building magmas of the two Réunion volcanoes. Fractional crystallization of lavas from both Piton de la Fournaise and Piton des Neiges begin well within the mantle at pressures up to 1 GPa which is significantly deeper than the crust-mantle boundary at about 12 km depth. The Réunion primary magmas form at an average depth of about 4 GPa in agreement with the thickness of the plate beneath the island. Lavas from both Réunion volcanoes have similar trace element compositions with the exception of lower Th/Ba for Piton des Neiges which implies a relatively homogeneous plume source during, at least, the last 2 Ma. The lack of any variation in the partial melting processes during this time span implies a thermal steady state of the plume centre. The Réunion lavas form either from a source that was enriched by partial melting or that contains recycled enriched MORB. Based on MORB- like Ce/Pb and Nb/U ratios an influence by fluid-metasomatized mantle, sediment or continental crustal material in the Réunion source appears unlikely. Received August 15, 2000; revised version accepted June 21, 2001     

Geochemistry of axial lavas from the mid- and southern Mariana Trough,and implications for back-arc magmatic processes

Mineralogy and Petrology - The Mariana Trough, a relatively simple intra-oceanic back-arc basin, is ideal for investigating magmatic processes and mantle-crust interaction in a subduction setting....     

Mantle sources and magma evolution of the Rooiberg lavas,Bushveld Large Igneous Province,South Africa

We report a new whole-rock dataset of major and trace element abundances and ⁸⁷Sr/⁸⁶Sr–¹⁴³Nd/¹⁴⁴Nd isotope ratios for basaltic to rhyolitic lavas from the Rooiberg continental large igneous province (LIP). The formation of the Paleoproterozoic Rooiberg Group is contemporaneous with and spatially related to the layered intrusion of the Bushveld Complex, which stratigraphically separates the volcanic succession. Our new data confirm the presence of low- and high-Ti mafic and intermediate lavas (basaltic—andesitic compositions) with >?4 wt% MgO, as well as evolved rocks (andesitic—rhyolitic compositions), characterized by MgO contents of <?4 wt%. The high- and low-Ti basaltic lavas have different incompatible trace element ratios (e.g. (La/Sm)_N, Nb/Y and Ti/Y), indicating a different petrogenesis. MELTS modelling shows that the evolved lavas are formed by fractional crystallization from the mafic low-Ti lavas at low-to-moderate pressures (~?4 kbar). Primitive mantle-normalized trace element patterns of the Rooiberg rocks show an enrichment of large ion lithophile elements (LILE), rare-earth elements (REE) and pronounced negative anomalies of Nb, Ta, P, Ti and a positive Pb anomaly. Unaltered Rooiberg lavas have negative εNd_i (??5.2 to ??9.4) and radiogenic εSr_i (6.6 to 105) ratios (at 2061 Ma). These data overlap with isotope and trace element compositions of purported parental melts to the Bushveld Complex, especially for the lower zone. We suggest that the Rooiberg suite originated from a source similar to the composition of the B1-magma suggested as parental to the Bushveld Lower Zone, or that the lavas represent eruptive successions of fractional crystallization products related to the ultramafic cumulates that were forming at depth. The Rooiberg magmas may have formed by 10–20% crustal assimilation by the fractionation of a very primitive mantle-derived melt within the upper crust of the Kaapvaal Craton. Alternatively, the magmas represent mixtures of melts from a primitive, sub-lithospheric mantle plume and an enriched sub-continental lithospheric mantle (SCLM) component with harzburgitic composition. Regardless of which of the two scenarios is invoked, the lavas of the Rooiberg Group show geochemical similarities to the Jurassic Karoo flood basalts, implying that the Archean lithosphere strongly affected both of these large-scale melting events.     

Geochemistry and origin of basaltic lavas from Marquesas Archipelago,French Polynesia

The Marquesas Archipelago, a volcanic chain in French Polynesia (south-central Pacific Ocean), is predominantly composed of alkalic, transitional and tholeiitic basalts. The variation trends in these intraplate basaltic rocks imply that the magmas were derived from different upper mantle sources. Model calculations using the total inverse method show that the peridotite source of most Marquesas basalts was enriched in incompatible elements compared to a primordial mantle and had higher than chondritic ratios of several elements such as La/Yb, Ti/V and P/Ce. A metasomatic enrichment event is suggested by the sequence of element enrichment in the source relative to the primordial mantle (Ba>Nb>La>Ce>Sr>Sm>Eu> Zr>Hf>Ti>Y>Yb). On the other hand, some lavas including tholeiites of Ua Pou and alkalic basalts of Hiva Oa, were probably derived from relatively depleted upper mantle. In some islands such as Hatutu, the different types of basalts were generated from sources with rather similar compositions. The residual phases of the Marquesas magmas included garnet. The sources of these magmas were similar in trace element chemistry to the oceanic mantle below Hawaii.     

Primitive off-rift basalts from Iceland and Jan Mayen: Os-isotopic evidence for a mantle source containing enriched subcontinental lithosphere

New measurements of Os, He, Sr and Nd isotopes, along with major and trace elements, are presented for basalts from the three volcanic flank zones in Iceland and from Jan Mayen Island. The ¹⁸⁷Os/¹⁸⁸Os ratios in lavas with <30 ppt Os (n = 4) are elevated compared to ratios in coexisting olivine and appear to be contaminated at a shallow level. The ¹⁸⁷Os/¹⁸⁸Os ratios in the remaining lavas with >30 ppt Os (n = 17) range between 0.12117 and 0.13324. These values are surprisingly low for oceanic island basalts and include some samples that are less than putative present-day primitive upper mantle (PUM with ¹⁸⁷Os/¹⁸⁸Os of 0.1296). These low ¹⁸⁷Os/¹⁸⁸Os preclude significant shallow-level contamination from oceanic crust. The ¹⁸⁷Os/¹⁸⁸Os ratios for Jan Mayen lavas are less than PUM, severely limiting the presence of any continental crust in their mantle source. A positive correlation between ¹⁴³Nd/¹⁴⁴Nd and ¹⁸⁷Os/¹⁸⁸Os ratios in Iceland and Jan Mayen lavas likely reflects the presence in their source of ancient subcontinental lithosphere that has undergone incompatible trace element enrichment that did not affect the Re-Os system. In addition, the Jan Mayen lava isotopic signature cannot be explained solely by the presence of subcontinental lithospheric mantle, and the influence of another geochemical component, such as a mantle plume appears required. Combined ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ³He/⁴He and ¹⁸⁷Os/¹⁸⁸Os data indicate a genetic relationship between Jan Mayen Island and the Iceland mantle plume. Material from the Iceland mantle plume likely migrates at depth until it reaches the tensional setting of the Jan Mayen Fracture Zone, where it undergoes low-degree partial melting. At a first-order, isotopic co-variations can be interpreted as broadly binary mixing curves between two primary end-members. One end-member, characterized in particular by its unradiogenic ¹⁸⁷Os/¹⁸⁸Os and ¹⁴³Nd/¹⁴⁴Nd, low ³He/⁴He and high ⁸⁷Sr/⁸⁶Sr, is represented by subcontinental lithospheric mantle stranded and disseminated in the upper mantle during the opening of the Atlantic Ocean. The second end-member corresponds to a hybrid mixture between the depleted-MORB mantle and the enriched Iceland mantle plume, itself resulting from mixing between recycled oceanic crust and depleted lower mantle. This hybrid accounts for the high ³He/⁴He (∼28 Ra), high ¹⁴³Nd/¹⁴⁴Nd (∼0.5132), high ¹⁸⁷Os/¹⁸⁸Os (∼0.14) and low ⁸⁷Sr/⁸⁶Sr (∼0.7026) composition observed in Iceland. Two different models may account for these observed mixing relationships between the end-members. In this first model, the Iceland mantle entrains pristine depleted material when rising in the upper mantle and allows refractory sub-lithospheric fragments to melt because of excess heat derived from the deep plume material. A second model that may better account for the Pb isotopic variations observed, uses the same components but where the depleted-MORB mantle is already polluted by subcontinental lithospheric mantle material before mixing with the Iceland mantle plume. Both cases likely occur. Though only three principal components are required to explain the isotopic variations of the Iceland-Jan Mayen system, the different possible mixing relationships may be accounted for by potentially a greater number of end-members.     

Geochemistry of basalt lavas from Vestfjella and adjacent areas,Dronning Maud Land,Antarctica

KAr ages, major- and trace-element compositions, and Sr-isotope data are presented for basalt lavas from Vestfjella, Dronning Maud Land, Antarctica. The new conventional KAr age data have yielded ages from 171 ± 2 to 695 ± 11 Ma, but the youngest (i.e. Middle Jurassic) ages are preferred. Mineralogical and chemical data show that the majority of the basalts are tholeiites. Petrographic mixing calculations, REE modelling, and the Sr isotope data suggest that they were derived by partial melting of garnet-free lherzolites with variable REE patterns, and subsequently modified by fractionation of olivine, Ca-rich pyroxene and plagioclase. Incompatible trace-element data from nearby Middle Jurassic basalt lavas (from Kirwanryggen and Heimefrontfjella) suggest a different source and REE modelling indicates generation from garnet lherzolites.     

Combined Sr,Nd, Pb and Li isotope geochemistry of alkaline lavas from northern James Ross Island (Antarctic Peninsula) and implications for back-arc magma formation

We present a comprehensive geochemical data set for a suite of back-arc alkaline volcanic rocks from James Ross Island Volcanic Group (JRIVG), Antarctic Peninsula. The elemental and isotopic (Sr, Nd, Pb and Li) composition of these Cenozoic basalts emplaced east of the Antarctic Peninsula is different from the compositions of the fore-arc alkaline volcanic rocks in Southern Shetlands and nearby Bransfield Strait. The variability in elemental and isotopic composition is not consistent with the JRIVG derivation from a single mantle source but rather it suggests that the magma was mainly derived from a depleted mantle with subordinate OIB-like enriched mantle component (EM II). The isotopic data are consistent with mantle melting during extension and possible roll-back of the subducted lithosphere of the Antarctic plate. Magma contamination by Triassic–Early Tertiary clastic sediments deposited in the back-arc basin was only localized and affected Li isotopic composition in two of the samples, while most of the basalts show very little variation in δ⁷Li values, as anticipated for “mantle-driven” Li isotopic composition. These variations are difficult to resolve with radiogenic isotope systematics but Li isotopes may prove sensitive in tracking complex geochemical processes acting through the oceanic crust pile, including hydrothermal leaching and seawater equilibration.     

Microstructural evidence for magma confluence and reusage of magma pathways: implications for magma hybridization,Karakoram Shear Zone in NW India

In the Karakoram Shear Zone, Ladakh, NW India, Miocene leucogranitic dykes form an extensive, varied and complex network, linking an anatectic terrane exposed in the Pangong Range, with leucogranites of the Karakoram Batholith. Mineral paragenesis of the heterogeneous anatectic source rocks suggests melting has resulted from water influx into rocks at upper amphibolite facies conditions, and microstructures suggest anatexis was contemporaneous with shearing. The network is characterized by continuous and interconnected dykes, with only rare cross‐cutting relationships, forming swarms and chaotic injection complexes where magmatic rocks cover up to 50% of the outcrop area. Despite this volume of magma, the system did not lose continuity, suggesting that it did not flow en masse and that the magma network was not all liquid simultaneously. Leucogranites in this network, including leucosomes in migmatites, carry an isotopic signature intermediate between the two main anatectic rocks in the source, suggesting efficient homogenization of the magmatic products. Here, we describe a number of microscopic features of these magmatic rocks which suggests that several pulses of magma used the same pathways giving rise to textural and chemical disequilibrium features. These include: (i) narrow, tortuous corridors of fine‐grained minerals cutting across or lining the boundaries of larger grains, interpreted to be remnants of magma‐filled cracks cutting across a pre‐existing magmatic rock; (ii) corrosion of early formed grains at the contact with fine‐grained material; (iii) compositional zoning of early formed plagioclase and K‐feldspar grains and quartz overgrowths documented by cathodoluminescence imaging; (iv) incipient development of rapakivi and anti‐rapakivi textures, and (iv) different crystallographic preferred orientation of early formed quartz and fine‐grained quartz. Mapping of the fine‐grained corridors interpreted to represent late melt channels reveal an interlinked network broadly following the S‐C fabric defined by pre‐existing magmatic grains. We conclude that early formed dykes provided a pathway exploited intermittently or continuously by new magma batches. New influxes of magma opened narrow channels and migrated through a microscopic network following predominantly grain boundaries along an S‐C fabric related to syn‐magmatic shearing. A mixed isotopic signature resulted not from the mixing of magmas, but from the micro‐scale interaction between new magma batches and previously crystallized magmatic rocks, through local equilibration.     

Geochemistry of granitic rocks from the Hercynian Sardinia-Corsica batholith: Implication for magma genesis

The Sardinia-Corsica batholith was structured in the late stage of the Hercynian orogenesis. The granitoids intrude mainly metamorphic complexes grading from zeolite up to amphibolite facies. The batholith is heterogeneous consisting of complexes with different affinity, chemical composition, age and degree of deformation. The present paper reports major-and trace-element data for selected samples coming only from Sardinian outcrops.

The rocks range from gabbro-diorite to tonalite, monzogranite and leucogranite. The two latter lithologies are the most abundant, gabbrodiorites and tonalites occurring in minor amounts and mainly in northern-central Sardinia. Over 75% of the granitoids contain microgranular enclaves of magmatic origin. The age of the rocks falls in the interval between 307 and 281 Ma. Sr isotope initial ratios are high, ranging between 0.7083 and 0.7107.

REE, Rb, Sr, Ba, Zr, Th, Ta, Hf, Co and Sc abundances were determined on selected samples. All elements follow three types of trends vs. CaO, which is used as differentiation index. Two trends show positive and negative correlations while the third one shows a bell-shaped pattern. LREE have different degrees of enrichment (La = 20−120× ch) and HREE show variable fractionation with prevailing (Tb/Yb)_n<1. The two peraluminous samples have very different geochemical characteristics.

From the geochemical point of view all the rocks coming from the Sardinian segment of the batholith display a typical calc-alkaline chemical character showing the imprint of both “normal and mature” continental arc geodynamic environments.

Geochemical trends suggest some petrogenetic constraints. The complete sequence of differentiation can be neither the product of crystal/liquid fractionation processes starting from a single basic parent magma nor the product of an AFC process. On the contrary, a two-stage model can be proposed. In the first stage a mafic melt of subcrustal origin interacted with monzogranitic magmas derived from 25–35% degree of melting of a crustal biotite amphibolitic source. Such a mixing process acted together with a crystal/liquid fractionation process to give tonalites and granodiorites. In the second stage lesser degrees of melting of the same crustal source could give the late-stage leucogranitic masses.

A possible scenario, able to take into account field and geochemical data, can be suggested for the genesis of this suite and we propose it as a working model for future investigations.     

滇西晚始新世高镁富钾火山岩的地球化学特征及其岩石成因机制探讨

40Ar/39Ar同位素定年分析显示滇西新生代高镁富钾火山岩均形成于始新世晚期(约36 Ma),富含MgO(＞9%)和K2O(3.07%～7.28%),绝大部分K2O/Na2O比值大于2,均属超钾质系列岩石.较高的Cr、Ni含量和较低的Sc(＜30 μg/g)、TiO2(＜1%)含量暗示了源区为尖晶石相方辉橄榄岩;高镁富钾火山岩与区内同时代的粗面岩具相似的地球化学组成特征,均富集LILE和LREE,亏损高场强元素Nb-Ta和Ti等,具有极低的Nb/La比值(0.2～0.3)、较高的87Sr/86Sr初始值(0.7056～0.7072)、负的εNd初始值(-0.97～-4.87)和相对较高的206pb/204Pb(18.556～18.695)、207pb/204Pb(15.609～15.630)比值,具有明显的岛弧型钾质火山岩的性质.高镁富钾火山岩来源于受古特提斯俯冲带流体交代的尖晶石相方辉橄榄岩的部分熔融岩浆,并在深部岩浆房经历了橄榄石的结晶分异和堆晶作用,而粗面岩则还在相对浅部岩浆房经历了较大程度的长石与单斜辉石的分离结晶.     

Geochemistry and evolution of Iherzolite-bearing phonolitic lavas from Nigeria,Australia, East Germany and New Zealand

The major and trace element chemistry of phonolites containing spinel Iherzolite xenoliths from Bokkos (Nigeria), Phonolite Hill (northeastern Australia) and Heldburg (East Germany) is consistent with an origin by fractional crystallization of basanitic magmas at upper mantle pressures (10–15 kbar). At Bokkos, spatially associated lavas ranging from hawaiitic nepheline mugearite to nepheline benmoreite can be modeled very well by fractional crystallization of kaersutitic amphibole + olivine + Fe-Ti-spinel + apatite, a crystal extract consistent with experimentally-determined near-liquidus phase relationships for mugearitic liquids. Further fractional crystallization of aluminous clinopyroxene + mica + apatite will yield the phonolites. A similar model relating the unusual Iherzolite-bearing mafic nepheline benmoreite from Pigroot (New Zealand) to basanitic lavas of the East Otago province is not supported by major and trace element data. The Pigroot lava is possibly the product of melting of a mantle source region previously enriched in Sr and light rare earth elements, with subsequent minor fractional crystallization of olivine + kaersutite. Dynamic flow crystallization processes operating within conduit systems from mantle pressures are capable of yielding large volumes of evolved phonolitic liquids from primary basanitic liquids, if magma flow rates are appropriate. This mechanism may provide an explanation for the volumetric bias towards salic differentiates in some alkalic provinces.     

Petrology and evolution of transitional alkaline — sub alkaline lavas from Patmos,Dodecanesos, Greece: evidence for fractional crystallization,magma mixing and assimilation

Petrographic, mineral chemical and whole-rock major oxide data are presented for the lavas of the Main Volcanic Series of Patmos, Dodecanesos, Greece. These lavas were erupted about 7 m.y. ago and range in composition from ne-trachybasalts through hy-trachybasalts and trachyandesites to Q-trachytes. To some extent, the ne-trachybasalts are intermediate in composition to the alkaline lavas found on oceanic islands and the calc-alkaline lavas of destructive plate margins. Major oxide variation is largely explicable in terms of fractional crystallization involving removal of the observed phenocryst and microphenocryst phases viz. olivine, plagioclase, clinopyroxene and Ti-magnetite in the mafic lavas, plagioclase, clinopyroxene, mica and Ti-magnetite in the evolved lavas. Apatite, which occurs as an inclusion in other phenocrysts or as microphenocrysts must also have been removed. However, mass balance calculations indicate that the chemistry of the hy-trachybasalts is inconsistent with an origin via fractional crystallization alone and the complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas show that they are hybrids formed by the mixing of 80-77% ne-trachybasalt with 20–23% trachyandesite. It is estimated that the mixing event preceded eruption by a period of 12 h-2 weeks suggesting that mixing triggered eruption. Combined fractionation and mixing cannot explain the relatively low MgO contents of the hy-trachybasalts and it is concluded that assimilation also occurred. Assimilation, and especially addition of volatiles to the magmas, may be responsible for the evolutionary trend from ne-normative to hy-normative magmas and was probably facilitated by intensified convection resulting from mixing. A model is presented whereby primitive magma undergoes fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot primitive magma into the base of the chamber facilitates assimilation, but eventually mixing yields the hy-trachybasalts and finally the ne-trachybasalts are erupted.     

High-Mg potassic rocks from Taiwan: implications for the genesis of orogenic potassic lavas

Taiwan is an active mountain belt formed by oblique collision between the Luzon arc and the Asian continent. Regardless of the ongoing collision in central and southern Taiwan, a post-collisional extension regime has developed since the Plio–Pleistocene in the northern part of this orogen, and led to generation of the Northern Taiwan Volcanic Zone. Emplaced at 0.2 Ma in the southwest of the Volcanic Zone, lavas from the Tsaolingshan volcano are highly magnesian (MgO≈15 wt.%) and potassic (K₂O≈5 wt.%; K₂O/Na₂O≈1.6–3.0). Whereas these basic rocks (SiO₂≈48 wt.%) have relatively low Al₂O₃≈12 wt.%, total Fe₂O₃≈7.5 wt.% and CaO≈7.2 wt.%, they are extremely enriched in large ion lithophile elements (LILE, e.g. Cs, Rb, Ba, Th and U). The Rb and Cs abundances, >1000 and 120 ppm, respectively, are among the highest known from terrestrial rocks. In addition, these rocks are enriched in light rare earth elements (LREE), depleted in high field strength elements (HFSE), and display a positive Pb spike in the primitive mantle-normalized variation diagram. Their REE distribution patterns mark with slight Eu negative anomalies (Eu/Eu*≈0.90–0.84), and Sr and Nd isotope ratios are uniform (⁸⁷Sr/⁸⁶Sr≈0.70540–0.70551; ¹⁴³Nd/¹⁴⁴Nd≈0.51268–0.51259). Olivine, the major phenocryst phase, shows high Fo contents (90.4±1.8; 1σ deviation), which are in agreement with the whole rock Mg-values (83–80). Spinel inclusions in olivine are characterized by high Cr/Cr+Al ratios (0.94–0.82) and have compositions similar to those from boninites that originate from highly refractory peridotites. Such petrochemical characteristics are comparable to the Group I ultrapotassic rocks defined by Foley et al. [Earth-Sci. Rev. 24 (1987) 81], such as orogenic lamproites from central Italy, Span and Tibet. We therefore suggest that the Tsaolingshan lavas resulted from a phlogopite-bearing harzburgitic source in the lithospheric mantle that underwent a recent metasomatism by the nearby Ryukyu subduction zone processes. The lavas exhibit unique incompatible trace element ratios, with Rb/Cs≈8, Ba/Rb≈1, Ce/Pb≈2, Th/U≈1 and Nb/U≈0.8, which are significantly lower than the continental crust values and those of most mantle-derived magmas. Nonmagmatic enrichment in the mantle source is therefore required. Based on published experimental data, two subduction-related metasomatic components, i.e., slab-released hydrous fluid and subducted sediment, are proposed, and the former is considered to be more pervasive for causing the extraordinary trace element ratios observed. Our observations lend support to the notion that dehydration from subducting slabs at convergent margins, as a continuing process through geologic time, can account for the fractionation of these elemental pairs between the Earth's crust and mantle.     

Generation of a crust-mantle magma mixture: magma sources and contamination at Cerro Panizos,central Andes

 Cerro Panizos, a large caldera in the central Andes Mountains, produced two large dacitic ignimbrites at 7.9 Ma and 6.7 Ma and many andesitic and dacitic lava flows and domes. The older rhyodacitic Cienago Ignimbrite represents the most silicic magma erupted by the system. The younger, much larger volume dacitic Cerro Panizos Ignimbrite is very crystal-rich, containing up to 50% biotite, plagioclase, and quartz crystals in the pumice. It is weakly zoned, with most of the zoning apparent between two main cooling units. Major and most trace elements show little variation through the Cerro Panizos Ignimbrite, but the small range of composition is consistent with typical fractionation trends. Sr, Nd, and Pb isotopic ratios are very “crustal”, with initial ⁸⁷Sr/⁸⁶Sr values of 0.711 to 0.715, ɛ_Nd values of –7.5 to –10.2, and nearly invariant Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb=18.85, ²⁰⁷Pb/²⁰⁴Pb=15.67, and ²⁰⁸Pb/²⁰⁴Pb=38.80). The limited zonation observed in the Cerro Panizos Ignimbrite is explained by impeded crystal settling due to high crystal content. The magma body was a crystal-liquid mush before ascent to the pre-eruption crustal levels. Crystals formed, but did not separate easily from the magma. Limited fractionation of plagioclase and biotite may have occurred, but the composition was largely controlled by lower crustal MASH processes. AFC modeling shows that the Cerro Panizos magmas resulted from a mixture of roughly equal proportions of late Miocene mantle-derived basalts and melts from ∼1.0 Ga (Grenville age) lower crust. This occurred in a MASH zone in the lower crust, and set the crustal isotopic ratios observed in the Cerro Panizos magmas. The great thickening of the crust beneath the central Andes Mountains sent upper and middle crustal rock types to lower crustal (and deeper) depths, and this explains the “upper crustal” isotopic signatures of the Cerro Panizos rocks. Minor upper crustal assimilation of early Miocene volcanic or subvolcanic rocks produced much of the isotopic variation seen in the system. The nearly invariant high Pb isotopic values and high Pb concentrations indicate that Pb came almost entirely from the crustal source, and was little altered by any subsequent upper crustal assimilation. This Pb signature is isotopically similar to that of the southern Bolivian Tin Belt, suggesting a widely distributed Pb source. The great difference between compositions of Miocene and Quaternary central Andean volcanic rocks is explained by crustal thickening in early Miocene time leading to abundant lower crustal water and associated fluxed melting during the time of the earlier eruptions. The lower crust dried out considerably by Quaternary time, so less crustal component is present. Received: 22 December 1994 / Accepted: 13 September 1995     

Geochemistry, age, and petrogenesis of rocks from the Garevka metamorphic complex, Yenisey Ridge

The mineralogical, petrological, geochemical and geochronological data on the Garevka metamorphic complex (GMC) of the Yenisey Ridge were used to evaluate the age, nature, and provenance of their protoliths. The evolution of the GMC occurred in two stages with different ages, thermodynamic regimes, and metamorphic field gradients. The final emplacement of granitoids was marked by high-pressure (HP) amphibolite facies regional metamorphism (970 Ma). At the second stage, these rocks experienced Late Riphean (900–870 Ma) retrograde epidote-amphibolite facies metamorphism accompanied by the formation of blastomylonitic complexes within narrow zones of brittle-ductile deformation. The metamorphism of migmatites (850 Ma) is coeval with the collisional medium-pressure metamorphism of the kyanite-sillimanite type. The GMC is different from the other rock complexes of the Yenisey Ridge in the presence of rapakivi-type granites. The geochemistry of these rocks, which is characterized by stronger enrichment in K₂O, FeO, Y, Th, U, Zr, Hf, Nb, Ta, and REE relative to the other mineral assemblages of the GMC, is typical of anorogenic (A-type) within-plate granites. Among other distinctive features of these rocks are the strong iron enrichment of the melanocratic minerals, the presence of ilmenite as the sole Fe-Ti oxide, and crystallization from higher temperature (T = 825°C vs. T = 750°C) water-poor magmas under reducing conditions below the FMQ buffer. Significant variations in the geochemical and petrological characteristics of the GMC rocks suggest that they could not be derived from a single source. The main volume of the high-K rocks varying in composition from A-type to S-type granites was generated by melting of mixed mantlecrustal sources. The products of melting of the Late Archean-Early Proterozoic infracrustal gneisses of the Siberian Craton could be a possible source for the least oxidized rocks.