Petrogenesis of gold-bearing listvenites from the carbonatized mantle section of the Neoproterozoic Ess ophiolite, Western Arabian Shield, Saudi Arabia

The variably serpentinized mantle peridotites of the Late Neoproterozoic Ess ophiolite (Western Saudi Arabia) are highly altered along shear zones and thrust planes to form erosion-resistant listvenites. The listvenites are distinguished petrographically and geochemically into three types: carbonate, silica-carbonate and silica (birbirite) listvenites. Geochemical analyses are consistent with expectations from petrography: carbonate listvenite is low in SiO₂ content but high in MgO, Fe₂O₃, and CaO relative to silica-carbonate and birbirite, which is remarkably high in SiO₂ at the expense of all other components. The total REE contents are low in silica-carbonate and carbonate listvenites but highly enriched in birbirite, with a large positive Eu anomaly. The host serpentinites have all the characteristics typically associated with highly depleted mantle harzburgite protoliths in supra-subduction fore-arc settings: bulk compositions are low in Al₂O₃ and CaO with high Mg# [molar Mg/(Mg + Fe)], relict Cr-spinel has high Cr# [molar Cr/(Cr + Al)] and low TiO₂, and relict olivine has high Mg# and NiO content. The Cr-spinel relics are also found in the listvenites; those in serpentinite and carbonate listvenites have significantly higher Mg# than those in silica-carbonate and birbirite, suggesting re-equilibration of Cr-spinel in the later phases of listvenitization. The varieties of listvenite capture successive stages of fluid-mediated replacement reactions. The carbonate listvenite appears to have developed syn-contemporaneously with serpentinization, whereas silica-carbonate listvenite and birbirite formed later. The listvenite formation resulted in leaching and removal of some components accompanied by deposition of others in the solid products, notably CO₃, SiO₂, REE (especially Eu), Au, Zn, As, Sb and K. Our data show that listvenitization concentrated gold at sub-economic to economic grades; measured gold concentrations in the host serpentinite are 0.5–1.7 ng/g, versus 4–2569 ng/g in carbonate listvenite, 43–3117 ng/g in silica-carbonate listvenite and 5–281 ng/g in birbirite. The listvenite deposits in the Jabal Ess area merit further exploration for gold

The common origin and alteration history of the hypabyssal and volcanic phases of the Wadi Tarr albitite complex, southern Sinai, Egypt

New data and interpretations are presented for the igneous albitites of the Wadi Tarr area, southern Sinai, Egypt. The albitite masses are isolated in outcrop from any granitic intrusions and have intrusive contacts against the country rocks without any structural control. They have marginal zones of breccias with jigsaw-fit angular clasts suggesting explosive, in-situ formation. The albitites are of two types: the western, medium-grained, hypabyssal albitite and the eastern, fine-grained porphyritic albitite. The field relations suggest emplacement at different levels in a magmatic cupola: the hypabyssal texture and steeply dipping slope of the upper contact of the western albitite imply deeper emplacement whereas the gently dipping contacts and porphyritic texture of the eastern albitite masses indicate that they define the probable location of the cupola apex. Both types of albitites consist of albite (92–97%) with minor amounts of quartz, K-feldspar and biotite. The accessory minerals include Fe-oxides, augite, sulphides, zircon, rutile, xenotime, titanite, allanite and monazite. The whole-rock compositions of the hypabyssal and porphyritic albitites are closely related, but the porphyritic type has lower abundances of Sr, Ba, Y, Nb, Th and Zr. We show that the hypabyssal and porphyritic albitites have a common petrogenetic origin, most likely as late-stage cumulates from a fractionating, strongly alkaline A-type magma, consistent with the compositions of the mafic minerals. The source magma was probably a tephritic liquid; we use MELTS models to show that only a sufficiently alkaline magma follows a differentiation path that both avoids quartz saturation and encounters the alkali feldspar solvus, reaching a residual liquid in equilibrium with highly sodic feldspar. Although the MELTS results show a chemically consistent means of forming igneous albitite, they are incomplete in that physical segregation mechanisms are still required to isolate the albite from mafic minerals and or a low-temperature aqueous alteration stage is needed to leach K from the feldspar. Alteration surrounding the Wadi Tarr albitites is extensive and dominated by alkali metasomatism similar to fenitization. Alteration in the marginal breccia zone of the albitite is dominated by precipitation of amphibole and carbonate in veins and in the breccia matrix, whereas the volcanic country rocks show replacement of feldspars by sericite, carbonate and epidote as well as vein carbonate. The altered volcanic country rocks show lower concentrations of Fe_2O_3, Sr, Cu, Pb, Ba and Ce, accompanied by higher concentrations of Na2O and MgO compared to unaltered equivalent samples

Petrological Characteristics of the Bou-azzer Ophiolote, Anti-atlas, Morocco : Nature of Proterozoic Oceanic Lithosphere

金沢大学大学院自然科学研究科Promoting Environmental Pesearch in Pan-Japan Sea Area : Young Researchers\u27 Network, Schedule: March 8-10,2006,Kanazawa Excel Hotel Tokyu, Japan, Organized by: Kanazawa University 21st-Century COE Program, Environmental Monitoring and Prediction of Long- & Short- Term Dynamics of Pan-Japan Sea Area ; IICRC(Ishikawa International Cooperation Research Centre), Sponsors : Japan Sea Research ; UNU-IAS(United Nations University Institute of Advanced Studies)+Ishikawa Prefecture Government ; City of Kanazaw

Petrogenesis of gold-bearing listvenites from the carbonatized mantle section of the Neoproterozoic Ess ophiolite, Western Arabian Shield, Saudi Arabia

The variably serpentinized mantle peridotites of the Late Neoproterozoic Ess ophiolite (Western Saudi Arabia) are highly altered along shear zones and thrust planes to form erosion-resistant listvenites. The listvenites are distinguished petrographically and geochemically into three types: carbonate, silica-carbonate and silica (birbirite) listvenites. Geochemical analyses are consistent with expectations from petrography: carbonate listvenite is low in SiO₂ content but high in MgO, Fe₂O₃, and CaO relative to silica-carbonate and birbirite, which is remarkably high in SiO₂ at the expense of all other components. The total REE contents are low in silica-carbonate and carbonate listvenites but highly enriched in birbirite, with a large positive Eu anomaly. The host serpentinites have all the characteristics typically associated with highly depleted mantle harzburgite protoliths in supra-subduction fore-arc settings: bulk compositions are low in Al₂O₃ and CaO with high Mg# [molar Mg/(Mg + Fe)], relict Cr-spinel has high Cr# [molar Cr/(Cr + Al)] and low TiO₂, and relict olivine has high Mg# and NiO content. The Cr-spinel relics are also found in the listvenites; those in serpentinite and carbonate listvenites have significantly higher Mg# than those in silica-carbonate and birbirite, suggesting re-equilibration of Cr-spinel in the later phases of listvenitization. The varieties of listvenite capture successive stages of fluid-mediated replacement reactions. The carbonate listvenite appears to have developed syn-contemporaneously with serpentinization, whereas silica-carbonate listvenite and birbirite formed later. The listvenite formation resulted in leaching and removal of some components accompanied by deposition of others in the solid products, notably CO₃, SiO₂, REE (especially Eu), Au, Zn, As, Sb and K. Our data show that listvenitization concentrated gold at sub-economic to economic grades; measured gold concentrations in the host serpentinite are 0.5–1.7 ng/g, versus 4–2569 ng/g in carbonate listvenite, 43–3117 ng/g in silica-carbonate listvenite and 5–281 ng/g in birbirite. The listvenite deposits in the Jabal Ess area merit further exploration for gold

パン・アフリカ帯の原生代オフィオライトのマントル部の岩石的性質

取得学位：博士(学術)，学位授与番号：博甲第856号，学位授与年月日：平成18年9月28

Genesis of peculiarly zoned Co, Zn and Mn-rich chromian spinel in serpentinite of Bou-Azzer ophiolite, Anti-Atlas, Morocco

金沢大学大学院自然科学研究科自然計測The peculiar Co, Zn and Mn-rich chromian spinels are hosted by magnetite veins, serpentinites and chromitites of the mantle section of the Proterozoic Bou-Azzer ophiolite, Morocco. The spinel is complexly zoned either optically or chemically, and exhibits anomalously high MnO, ZnO and CoO contents (up to 22, 7.5 and 2 wt%, respectively). It has four distinct optical zones particularly in the magnetite veins and less typically in serpentinites. The highest level of these elements, probably divalent, is recorded within the ferritchromite zone and/or within the core zone if the ferritchromite zone is absent. These elements as well as Fe exhibit enrichment along grain boundaries and fractures of the altered spinels. Fe, Mn, Zn and Co were most probably supplied from olivine upon severe serpentinization during and after obduction of the ophiolite. The enrichment of the Bou-Azzer chromian spinel in Mn, Zn and Co was governed mainly by the fluid/mineral (spinel) ratio and partition coefficient between spinel and the relevant fluid among many factors. The Co-, Zn- and Mn-rich chromian spinels can be used as an exploration guide for Co-Ni-Zn-Cu sulfide mineralization associated with serpentinized peridotites

Late Ediacaran post-collisional A-type syenites with shoshonitic affinities, northern Arabian-Nubian Shield: a possible mantle-derived A-type magma

The Abu Rumeil syenitic rocks represent the inner ring dyke of the Katherina Ring complex, southern Sinai, Egypt. They are divided petrologically into two types, alkali feldspar syenite and quartz syenite. The mineralogy and geochemistry of the syenites indicate an alkaline nature with a shoshonitic affinity. Although rare mafic xenocrysts overgrown by primary K-feldspars and overlapping rare earth element (REE) patterns indicate some role for crustal contamination, the trace element chemistry shows a dominant mantle contribution. The geochronology and field relations imply that the Abu Rumeil syenites were emplaced in a post-collisional, within-plate tectonic setting, yet they express the enrichments in large-ion lithophile elements relative to high field strength elements generally characteristic of subduction influence. We suggest that this signature is inherited from partial melting of a lithospheric mantle source previously affected by subduction during assembly of the Arabian-Nubian Shield. Little evidence of the early evolution of the suite is preserved; there are no associated mafic rocks. We therefore restrict our attention to a petrogenetic model that can explain the relations among the observed felsic composition. The REE patterns of all samples are enriched in light REE and fractionated, but it is notable that there are small positive Eu anomalies in the alkali-feldspar syenites contrasting with small negative Eu anomalies in the quartz syenites. Positive Eu anomalies suggest a cumulate nature for the alkali-feldspar syenites; there are also breaks in the slopes of most variation trends between the alkali-feldspar syenites and the quartz syenites. The general trends in all major oxides and trace elements within the suite can be modeled by fractional crystallization of feldspars—with smaller roles for pyroxene, biotite, apatite, and Fe-Ti oxides—from an intermediate liquid to form the quartz syenites and by assimilation of the near-liquidus phases into the same starting liquid to form the alkali feldspar syenites. The geothermobarometry of pyroxenes and amphiboles suggests shallow emplacement (<10 km depth) and crystallization temperatures ranging from 1100 °C down to 800 °C

Late Ediacaran post-collisional A-type syenites with shoshonitic affinities, northern Arabian-Nubian Shield: a possible mantle-derived A-type magma

The Abu Rumeil syenitic rocks represent the inner ring dyke of the Katherina Ring complex, southern Sinai, Egypt. They are divided petrologically into two types, alkali feldspar syenite and quartz syenite. The mineralogy and geochemistry of the syenites indicate an alkaline nature with a shoshonitic affinity. Although rare mafic xenocrysts overgrown by primary K-feldspars and overlapping rare earth element (REE) patterns indicate some role for crustal contamination, the trace element chemistry shows a dominant mantle contribution. The geochronology and field relations imply that the Abu Rumeil syenites were emplaced in a post-collisional, within-plate tectonic setting, yet they express the enrichments in large-ion lithophile elements relative to high field strength elements generally characteristic of subduction influence. We suggest that this signature is inherited from partial melting of a lithospheric mantle source previously affected by subduction during assembly of the Arabian-Nubian Shield. Little evidence of the early evolution of the suite is preserved; there are no associated mafic rocks. We therefore restrict our attention to a petrogenetic model that can explain the relations among the observed felsic composition. The REE patterns of all samples are enriched in light REE and fractionated, but it is notable that there are small positive Eu anomalies in the alkali-feldspar syenites contrasting with small negative Eu anomalies in the quartz syenites. Positive Eu anomalies suggest a cumulate nature for the alkali-feldspar syenites; there are also breaks in the slopes of most variation trends between the alkali-feldspar syenites and the quartz syenites. The general trends in all major oxides and trace elements within the suite can be modeled by fractional crystallization of feldspars—with smaller roles for pyroxene, biotite, apatite, and Fe-Ti oxides—from an intermediate liquid to form the quartz syenites and by assimilation of the near-liquidus phases into the same starting liquid to form the alkali feldspar syenites. The geothermobarometry of pyroxenes and amphiboles suggests shallow emplacement (<10 km depth) and crystallization temperatures ranging from 1100 °C down to 800 °C

On the relative timing of listwaenite formation and chromian spinel equilibration in serpentinites

Ultramafic rocks exposed at the Earth's surface generally record multiple stages of evolution that may include melt extraction, serpentinization, carbonatization, and metamorphism. When quantitative thermometry based on mineral chemistry is applied to such rocks, it is often unclear what stage of their evolution is being observed. Here, in peridotites with extensive replacement of silicate minerals by carbonates (listwaenites), we present a case study that addresses the timing of carbonate formation relative to closure of exchange reactions among relict primary minerals. Massive and schistose serpentinized peridotites of Neoproterozoic age outcrop at Gabal Sirsir, South Eastern Desert, Egypt (northwestern corner of the Arabian-Nubian Shield or ANS). Petrography, bulk composition, and mineral chemistry are all consistent with a strongly depleted mantle harzburgite protolith for the serpentinites. Bulk compositions are low in Al_2O_3 and CaO and high in Mg# [molar Mg/(Mg+Fe) = 0.89–0.93]. Relict spinel has high Cr# [molar Cr/(Cr+Al)] and low Ti, while relict olivine has high Mg# and NiO contents. Based on compositions of coexisting relict olivine and chromian spinel, the protolith experienced 19 to 21% partial melt extraction. Such high degrees of partial melting indicate a supra-subduction zone environment, possibly a forearc setting. Along thrust faults and shear zones, serpentinites are highly altered to form talc-carbonate rocks and weathering-resistant listwaenites that can be distinguished petrographically into Types I and II. The listwaenitization process took place through two metasomatic stages, associated first with formation of the oceanic crustal section and near-ridge processes (∼750–700 Ma) and subsequently during obduction associated with the collision of East and West Gondwana and escape tectonics (∼650–600 Ma). In the first stage, Mg# of chromian spinel in the serpentinites continuously changed due to subsolidus Mg–Fe^(2+) redistribution, while the Mg# of chromian spinel in the Type I listwaenites was frozen due to the absence of coexisting mafic silicates. During the second stage, the Type II listwaenites formed along shear zones accompanied by oxidation of relict chromian spinel to form ferritchromite and Cr-bearing magnetite in both serpentinites and listwaenites. The high Cr# of chromian spinel relics in both serpentinites and listwaenites preserves primary evidence of protolith melt extraction, but divalent cations are more easily mobilized at low temperature. Hence, relict chromian spinel in listwaenites shows significantly higher Mg# and lower MnO than that in serpentinite, suggesting that nearly complete alteration of ultramafic rocks to form listwaenite took place prior to re-equilibration between chromian spinel and the surrounding mafic minerals in serpentinites. Furthermore, the ferritchromite in the serpentinites has higher Mn content (1.1–2.1 wt%) than that in the listwaenites (0.6–0.9 wt%), indicating its formation after carbonatization since carbonate minerals are a favorable sink for Mn