71 research outputs found

    Aluminous websterite and granulite xenoliths from the Chyulu Hills volcanic field, Kenya: gabbro-troctolitic cumulates subjected to lithospheric foundering

    Get PDF
    Whole rock major and trace element abundances in aluminous garnet-spinel websterite, sapphirine-bearing Mg-Al granulite and hibonite-bearing Ca-Al granulite xenoliths from the Chyulu Hills volcanic field, Kenya, suggest that the samples represent a meta-igneous suite linked by fractionation. The incompatible major element contents increase from the websterites to the Mg-Al granulites and further to the Ca-Al granulites. High bulk rock Mg#s and very low concentrations of most incompatible trace elements indicate that the rocks are cumulates rather than crystallized melts. Elevated Ni abundances, impoverishment in Cr and HFSE and high contents of normative plagioclase and olivine in the granulites indicate that their protoliths were similar to troctolite. The textures and metamorphic reaction paths recorded in the granulites suggest igneous emplacement in the crust and cooling from igneous to ambient crustal temperatures accompanied or followed by compression. For the websterite xenoliths, there is an apparent contradiction between the results of P-T calculations that suggest high P and T of crystallization of early generation pyroxenes and elevated P-T conditions during final equilibration (1.4-2.2GPa/740-980°C) on the one hand and the positive Eu anomaly that suggests shallow-level plagioclase accumulation on the other hand. This contradiction can be reconciled by a model of compression of a plagioclase-bearing (gabbroic) protolith to mantle depths where it recrystallized to an ultramafic assemblage, which requires foundering of dense lower crustal material into the mantl

    Entrained Macrocryst Minerals as a Key to the Source Region of Olivine Nephelinites: Humberg, Kaiserstuhl, Germany

    Get PDF
    Olivine nephelinites commonly contain macrocrysts of olivine and clinopyroxene. Some of these macrocrysts might represent fragments of the source region of the host magma transported to the Earth's surface. If this hypothesis is correct these fragments can be used to characterize the composition of the source region and to put constraints on the magma generation process. In this study, we investigate the origin of macrocrysts and mineral aggregates from an olivine nephelinite from the Kaiserstuhl, Germany. We focus on clinopyroxenes (Cpx), which can be divided into three groups. Cpx I is relict Cpx from aggregates with deformed olivine that is depleted in Ca and characterized by strong light rare earth element (LREE) fractionation, low Ti/Eu and negative high field strength element (HFSE) anomalies. Its geochemical signature is consistent with formation by carbonatite metasomatism and with equilibration in the presence of orthopyroxene. Cpx II is Ca-rich Cpx, forming both aggregates with deformed olivine and individual macrocrysts. The LREE, as for Cpx I, are strongly fractionated. Convex REE patterns may be present. The depletion in HFSE is less pronounced. Cpx III is oscillatory zoned Cpx phenocrysts showing enrichment in Ca, convex REE patterns and no HFSE anomalies. The transition in the trace element abundances between the Cpx of the three groups is gradual. However, Cpx I and II did not crystallize from the host magma, as demonstrated by the presence of kink-bands and undulose extinction in the associated olivine and by the composition of alkali aluminosilicate glass inclusions in Cpx II. Based on the Cpx relationships, we interpret the studied suite of macrocrysts and mineral aggregates as a mixture of disintegrated fragments of the source region of the host olivine nephelinite. The process of melt generation was multi-stage. A primary carbonatite melt ascending from deeper levels in the mantle, probably from the dolomite-garnet peridotite stability field, reacted with mantle peridotite along the solidus ledge in the system lherzolite-CO2 (< 20-22 kbar) and started to crystallize carbonate minerals. Because of its low solidus temperature, the resulting carbonate-wehrlite assemblage melted incongruently with the formation of additional clinopyroxene. The carbonatite melt evolved during crystallization of carbonate minerals and concomitant incongruent melting of the carbonate-wehrlite, accompanied by the segregation of incipient alkali aluminosilicate melts. As a consequence of fast reaction rates in the presence of a carbonatite melt, this process probably took place under disequilibrium conditions. Further melting of the assemblage wehrlite + alkali aluminosilicate melt led to the generation of the olivine nephelinite magma. It entrained fragments of the wehrlite and brought them to the surfac

    Petrological Evolution of the Magmatic Suite Associated with the Coroccohuayco Cu(-Au-Fe) Porphyry-Skarn Deposit, Peru

    Get PDF
    The petrological evolution of magmatic rocks associated with porphyry-related Cu deposits is thought to exert a first-order control on ore genesis. It is therefore critical to understand and recognize petrological processes favourable to the genesis of porphyry systems. In this study we present new petrographic, geochemical (whole-rock and mineral), and isotopic (Pb, Sr, Nd) data for rocks from the magmatic suite associated with the Eocene Coroccohuayco porphyry-skarn deposit, southern Peru. Previously determined radiometric ages on these rocks provide the temporal framework for interpretation of the data. Arc-style magmatic activity started at Coroccohuayco with the emplacement of a composite precursor gabbrodiorite complex at c. 40·4 Ma. After a nearly 5 Myr lull, magmatic activity resumed at c. 35·6 Ma with the rapid emplacement of three dacitic porphyries associated with mineralization. However, zircon antecrysts in the porphyries show that intra-crustal magmatic activity started c. 2 Myr before porphyry emplacement and probably built a large intra-crustal magmatic body with an associated large thermal anomaly. Our data suggest that all magmas underwent a period of evolution in the deep crust before transfer and further evolution in the upper crust. The gabbrodiorite complex was sourced from a heterogeneous deep crustal reservoir and was emplaced at a pressure of 100-250 MPa where it underwent a limited amount of fractionation and formed a chemically zoned pluton. Its initial water content and oxygen fugacity were estimated to be around 3 wt % H2O and NNO ± 1 (where NNO is the nickel-nickel oxide buffer), respectively. The deep crustal source of the porphyries appears to have been more homogeneous. The porphyries are interpreted to be the product of advanced differentiation of a parental magma similar to the gabbrodiorite. Most of this evolution occurred at deep crustal levels (around 800 MPa) through fractionation of amphibole + pyroxene + plagioclase ± garnet, leading to the development of a high Sr/Y signature characteristic of porphyry-related magmatism worldwide. Subsequent upper crustal evolution (100-250 MPa) was dominated by crustal assimilation, cannibalism of previously emplaced magma batches (proto-plutons) and magma recharge. Water content and oxygen fugacity were estimated to be around 5 wt % H2O and NNO + 1 to NNO + 2, respectively, at the end of the period of upper crustal evolution. This high oxygen fugacity is inferred to have favoured sulphur and metal enrichment in the melt. The high thermal regime generated through 2 Myr of sustained magmatism in the upper crust favoured crustal assimilation, proto-pluton cannibalism, and efficient metal extraction upon fluid exsolution. The Coroccohuayco magmatic suite appears to have acquired its metallogenic potential (high fO2, high Sr/Y) through several million years of deep crustal evolutio

    Trace Element Partitioning in HP-LT Metamorphic Assemblages during Subduction-related Metamorphism, Ile de Groix, France: a Detailed LA-ICPMS Study

    Get PDF
    Devolatilization reactions and subsequent transfer of fluid from subducted oceanic crust into the overlying mantle wedge are important processes, which are responsible for the specific geochemical characteristics of subduction-related metamorphic rocks, as well as those of arc magmatism. To better understand the geochemical fingerprint induced by fluid mobilization during dehydration and rehydration processes related to subduction zone metamorphism, the trace element and rare earth element (REE) distribution patterns in HP-LT metamorphic assemblages in eclogite-, blueschist- and greenschist-facies rocks of the Ile de Groix were obtained by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) analysis. This study focuses on 10 massive basic rocks representing former hydrothermally altered mid-ocean ridge basalts (MORB), four banded basic rocks of volcano-sedimentary origin and one micaschist. The main hosts for incompatible trace elements are epidote (REE, Th, U, Pb, Sr), garnet [Y, heavy REE (HREE)], phengite (Cs, Rb, Ba, B), titanite [Ti, Nb, Ta, REE; HREE > LREE (light REE)], rutile (Ti, Nb, Ta) and apatite (REE, Sr). The trace element contents of omphacite, amphibole, albite and chlorite are low. The incompatible trace element contents of minerals are controlled by the stable metamorphic mineral assemblage and directly related to the appearance, disappearance and reappearance of minerals, especially epidote, garnet, titanite, rutile and phengite, during subduction zone metamorphism. Epidote is a key mineral in the trace element exchange process because of its large stability field, ranging from lower greenschist- to blueschist- and eclogite-facies conditions. Different generations of epidote are generally observed and related to the coexisting phases at different stages of the metamorphic cycle (e.g. lawsonite, garnet, titanite). Epidote thus controls most of the REE budget during the changing P-T conditions along the prograde and retrograde path. Phengite also plays an important role in determining the large ion lithophile element (LILE) budget, as it is stable to high P-T conditions. The breakdown of phengite causes the release of LILE during retrogression. A comparison of trace element abundances in whole-rocks and minerals shows that the HP-LT metamorphic rocks largely retain the geochemical characteristics of their basic, volcano-sedimentary and pelitic protoliths, including a hydrothermal alteration overprint before the subduction process. A large part of the incompatible trace elements remained trapped in the rocks and was recycled within the various metamorphic assemblages stable under changing metamorphic conditions during the subduction process, indicating that devolatilization reactions in massive basic rocks do not necessarily imply significant simultaneous trace element and REE releas

    Discovery of an albite gneiss from the Ile de Groix (Armorican Massif, France): geochemistry and LA-ICP-MS U-Pb geochronology of its Ordovician protolith

    Get PDF
    For the first time, an albite orthogneiss has been recognised and dated within the HP-LT blueschist facies metabasites and metapelites of the Ile de Groix. It is characterised by a peraluminous composition, high LILE, Th and U contents, MORB-like HREE abundances and moderate Nb and Y values. A U-Pb age of 480.8±4.8Ma was obtained by LA-ICP-MS dating of zircon and titanite. It is interpreted as the age of the magmatic emplacement during the Early Ordovician. Morphologically different zircon grains yield late Neoproterozoic ages of 546.6-647.4Ma. Zircon and titanite U-Pb ages indicate that the felsic magmatism from the Ile de Groix is contemporaneous with the acid, pre-orogenic magmatism widely recognised in the internal zones of the Variscan belt, related to the Cambro-Ordovician continental rifting. The magmatic protolith probably inherited a specific chemical composition from a combination of orogenic, back-arc and anorogenic signatures because of partial melting of the Cadomian basement during magma emplacement. Besides, the late Devonian U-Pb age of 366±33Ma obtained for titanite from a blueschist facies metapelite corresponds to the age of the HP-LT peak metamorphis

    Data on the arc magmatism developed in the Antarctic Peninsula and Patagonia during the Late Triassic – Jurassic: A compilation of new and previous geochronology, geochemistry and isotopic tracing results

    Get PDF
    We present the results of U-Pb zircon dating conducted using laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS), isotopic tracing analyses of Hf in zircon and Sr-Nd in whole-rock and whole-rock major oxides, and trace element abundances of 12 plutonic and volcanic rocks present on the Antarctic Peninsula. The dataset is presented in combination with the results of previous studies conducted in both Patagonia and the Antarctic Peninsula. These results were filtered for concordant 206Pb–238U zircon ages and topology of the 40Ar/39Ar age spectra. These results may be useful for researchers studying the geological evolution of southern Gondwana, West Antarctica or Patagonia. The interpretation of this dataset is found in the co-submitted paper by Bastias, et al. (2021a) titled ‘A revised interpretation of the Chon Aike magmatic province: active margin origin and implications for the opening of the Weddell Sea’
    corecore