Petrology of the mafic rocks of the Xigaze ophiolite,Tibet

The Xigaze ophiolite (Yarlung-Zangbo suture zone, Southern Tibet, China) shows an unusual crustal sequence characterized by a lack of large masses of cumulate gabbros, by dolerites intrusive throughout the whole ophiolite sequence, and by the injection of dolerites in already serpentinized peridotites. The abyssal tholeiitic nature of all the mafic rocks indicates that they have been generated at an oceanic ridge. All the geological arguments and petrological and textural data on the mafic rocks point to very low heat production and large heat losses through widespread intensive sea-water circulation, for the spreading centre in which they have been formed, in good agreement with a slow-spreading ridge origin.     

Deep and High-temperature Hydrothermal Circulation in the Oman Ophiolite--Petrological and Isotopic Evidence

A systematic search for evidence of high-temperature hydrousalteration within the gabbros of the Samail ophiolite (Oman)shows that most of the gabbros have been affected by successivestages of alteration, starting above 975°C and ending below500°C. Sr and O isotopic analyses provide constraints onthe nature and origin of the fluids associated with these alterationevents. Massive gabbros, dykes and veins and their associatedminerals depart from mid-ocean ridge basalt (MORB)-source magmasignatures (⁸⁷Sr/⁸⁶Sr >0·7032 and depleted     

Hydrous partial melting within the lower oceanic crust

We studied more than 60 oceanic gabbros from the recent oceanic crust and from ophiolites (East Pacific Rise, Mid-Atlantic Ridge, Southwest Indian Ridge, Oman ophiolite) by scanning electron microscopy and found in nearly all samples microstructures suggesting that hydrous partial melting reactions proceeded. The characteristic paragenesis consists of orthopyroxene and pargasite rimming olivine and clinopyroxene primocrysts in intimate contact with neoblastic plagioclase strongly enriched in anorthite. This is in agreement with recent water-saturated melting experiments on a variety of natural gabbros between 900 and 1000 °C. The observed microtextures in the natural gabbros imply the propagation of water-rich fluids on grain boundaries in a ductile regime causing hydrous partial melting. Thus, this type of hydrothermal activity proceeds within the deep oceanic crust at very high temperatures (900–1000 °C) without a crack system, a prerequisite in current models for enabling hydrothermal circulation.     

Geology and geochemistry of the Shuanggou ophiolite (Ailao Shan ophiolitic belt), Yunnan Province, SW China: Evidence for a slow-spreading oceanic basin origin

The early Carboniferous Shuanggou ophiolite lies in the middle segment of the Ailao Shan orogenic belt between the South China Block to the north and the Indochina Block to the south. The ophiolite consists of meta-peridotite, gabbro, diabase and basalt, capped by radiolarian-bearing siliceous rocks. No layered gabbros or sheeted dikes have been observed. The meta-peridotite underwent low degrees of partial melting, consistent with the low magma budget of this oceanic lithosphere. Whole-rock rare earth element analyses of gabbro indicate a geochemical affinity with normal mid-ocean ridge basalts, consistent with the crystallization order of plagioclase followed by clinopyroxene recognized in the gabbros. The ophiolite is believed to have formed in a small, slow-spreading oceanic basin. Collision of the Indochina Block with the South China Block in the late Paleozoic was responsible for the closure of the oceanic basin and emplacement of the ophiolite in the Ailao Shan orogenic belt.     

Alteration of the oceanic crust: Implications for geochemical cycles of lithium and boron

Fresh tholeiitic basalt glass has been reacted with seawater at 150°C, (water/rock mass ratio of 10), and fresh diabase has been reacted with a Na-K-Ca-Cl fluid at 375°C (water/rock mass ratios of 1, 2, and 5) to understand better the role of temperature, basalt composition, and water/rock mass ratio on the direction and magnitude of B and Li exchange during basalt alteration. At 150°C, slight but nevertheless significant amounts of B and Li were removed from seawater and incorporated into a dominantly smectite alteration phase. At 375°C, however, B and Li were leached from basalt. B behaved as a “soluble” element and attained concentrations in solution limited only by the B concentration in basalt and the water/rock mass ratio. Li, however, was less mobile. For example, at water/rock mass ratios of 1, 2, and 5, the percent of Li leached from basalt was 58, 70, and 92% respectively. This suggests some mineralogic control on Li mobility during hydrothermal alteration of basalt, especially at low-water/rock mass ratios. In general, these results, as well as those for B, are consistent with the temperature-dependent chemistry of altered seafloor basalt and the chemistry of ridge crest hydrothermal fluids.Based on the distribution and chemistry of products of seafloor weathering, low (≤ 150°C) and high-temperature hydrothermal alteration of basalt, and the chemistry of ridge crest hydrothermal fluids, it was estimated that alteration of the oceanic crust is a Li source for seawater. This is not true for B, however, since the hot spring flux estimated for B is balanced by low-temperature basalt alteration. These data, coupled with B and Li flux estimates for other processes (e.g., continental weathering, clay mineral adsorption, authigenic silicate formation and formation of siliceous skeletal material) yield new insight into the B and Li geochemical cycles. Calculations performed here indicate relatively good agreement between the magnitude of B and Li sources and sinks. The geochemical cycle of B, however, may be affected by serpentinization of mantle derived peridotite in oceanic fracture zones. Serpentinites are conspicuously enriched in B and if the B source for these rocks is seawater, then an additional B sink exists which must be integrated into the B geochemical cycle. However, until more data are available in terms of areal extent of serpentinization, serpentite chemistry and isotopic composition, the importance of B in these rocks with respect to the B geochemical cycle remains speculative at best.     

Progressive metamorphism of the Taitao ophiolite; evidence for axial and off-axis hydrothermal alterations

We estimated metamorphic conditions for the  6 Ma Taitao ophiolite, associated with the Chile triple junction. The metamorphic grade of the ophiolite, estimated from secondary matrix minerals, changes stratigraphically downwards from the zeolite facies, through the prehnite–actinolite facies, greenschist facies and the greenschist–amphibolite transition, to the amphibolite facies. The metamorphic facies series corresponds to the low-pressure type. The metamorphic zone boundaries are subparallel to the internal lithological boundaries of the ophiolite, indicating that the metamorphism was due to axial hydrothermal alteration at a mid-ocean ridge.

Mineral assemblages and the compositions of veins systematically change from quartz-dominated, through epidote-dominated, to prehnite-dominated with increasing depth. Temperatures estimated from the vein assemblages range from  230 °C in the volcanic unit to  380 °C at the bottom of the gabbro unit, systematically  200 °C lower than estimates from the adjoining matrix minerals. The late development of veins and the systematically lower temperatures suggest that the vein-forming alteration was due to off-axis hydrothermal alteration.

Comparison between the Taitao ophiolite with its mid-ocean ridge (MOR) affinity, and other ophiolites and MOR crusts, suggests that the Taitao ophiolite has many hydrothermal alteration features similar to those of MOR crusts. This is consistent with the tectonic history that the Taitao ophiolite was formed at the South Chile ridge system near the South American continent (Anma, R., Armstrong, R., Danhara, T., Orihashi, Y. and Iwano, H., 2006. Zircon sensitive high mass-resolution ion microprobe U–Pb and fission-track ages for gabbros and sheeted dykes of the Taitao ophiolite, Southern Chile, and their tectonic implications. The Island Arc, 15(1): 130–142).     

Origin and tectonic significance of corundum–kyanite–sapphirine amphibolites from the Variscan French Massif Central

The contact zone between two major allochthonous lithotectonic units in the French Massif Central (FMC) is characterized by the presence of corundum‐bearing amphibolites associated with serpentinites, flaser‐gabbros, eclogites and granulites. These unusual amphibolites are best preserved in the Western FMC, where they are found within the lower oceanic crust of the Limousin ophiolite. Mineralogical observations and thermodynamic modelling of the spinel–corundum–sapphirine–kyanite amphibolites in the CMASH system show that they were formed at peak P–T conditions around 800 °C/10 kbar in response to near isothermal burial followed by a retrogressive anticlockwise path. Metamorphic reactions are controlled both by modification of P–T conditions and by local chemical changes linked to fluid infiltration. Pargasite growth has been enhanced by infiltration of Ca‐ and Al‐rich fluids whereas kyanite‐ and sapphirine‐forming reactions are partly controlled by local inputs of MgO–SiO₂ components, most probably during infiltration metasomatism. By analogy with worldwide ophiolites (Oman, Tethyan, Appalachian) and published numerical models, subduction of a still‐hot oceanic ridge is proposed to form these Al‐rich amphibolites from plagioclase‐rich troctolites. The trace‐element composition of high‐Ti, fine‐grained amphibolites (former fine‐grained Fe–Ti gabbros) adjacent to the corundum‐bearing ones, further indicates that the oceanic crust was initially created at a mid‐ocean ridge (rather than within a back‐arc basin), followed by the emplacement of supra‐subduction zone‐type magmas, probably due to intraoceanic subduction close to the ridge.     

Petrological evidence for stepwise accretion of metamorphic soles during subduction infancy (Semail ophiolite,Oman and UAE)

Metamorphic soles are tectonic slices welded beneath most large‐scale ophiolites. These slivers of oceanic crust metamorphosed up to granulite facies conditions are interpreted as forming during the first million years of intraoceanic subduction following heat transfer from the incipient mantle wedge towards the top of the subducting plate. This study reappraises the formation of metamorphic soles through detailed field and petrological work on three key sections from the Semail ophiolite (Oman and United Arab Emirates). Based on thermobarometry and thermodynamic modelling, it is shown that metamorphic soles do not record a continuous temperature gradient, as expected from simple heating by the upper plate or by shear heating as proposed in previous studies. The upper, high‐T metamorphic sole is subdivided in at least two units, testifying to the stepwise formation, detachment and accretion of successive slices from the down‐going slab to the mylonitic base of the ophiolite. Estimated peak pressure–temperature conditions through the metamorphic sole, from top to bottom, are 850°C and 1 GPa, 725°C and 0.8 GPa and 530°C and 0.5 GPa. These estimates appear constant within each unit but differing between units by 100–200°C and ~0.2 GPa. Despite being separated by hundreds of kilometres below the Semail ophiolite and having contrasting locations with respect to the ridge axis position, metamorphic soles show no evidence for significant petrological variations along strike. These constraints allow us to refine the tectonic–petrological model for the genesis of metamorphic soles, formed via the stepwise stacking of several homogeneous slivers of oceanic crust and its sedimentary cover. Metamorphic soles result not so much from downward heat transfer (ironing effect) as from progressive metamorphism during strain localization and cooling of the plate interface. The successive thrusts originate from rheological contrasts between the sole, initially the top of the subducting slab, and the peridotite above as the plate interface progressively cools. These findings have implications for the thickness, the scale and the coupling state at the plate interface during the early history of subduction/obduction systems.     

新疆西准噶尔达拉布特蛇绿岩E-MORB型镁铁质岩的地球化学、年代学及其地质意义

新疆西准噶尔地区是古生代经过俯冲-增生形成的复合造山带,该地区分布有多条蛇绿岩带,其中之一的西准噶尔达拉布特蛇绿岩被认为是最大的一条蛇绿岩带,可能代表了古亚洲洋壳的残余。本文的资料显示蛇绿岩带内的镁铁质岩呈现出N-MORB、E-MORB和似OIB的地球化学特征,通过对阿克巴斯套岩体中的浅色辉长岩LA-ICP-MS锆石年龄测定,获得达拉布特蛇绿岩E-MORB型镁铁质岩的年龄为302±1.7Ma。鉴于达拉布特蛇绿岩中E-MORB和似OIB型镁铁质岩成因的复杂性,结合前人研究成果,对辉长岩锆石U-Pb年龄所代表的意义存在两种可能性：（1）E-MORB型和似OIB型镁铁质岩可能是弧后盆地扩张后期的产物,代表蛇绿岩的年龄,其表明西准噶尔地区可能晚石炭纪还有洋盆存在;（2）E-MORB型镁铁质岩是蛇绿岩消亡阶段由于扩张脊和俯冲带碰撞作用而形成的弧前海山,形成时代晚于达拉布特主体蛇绿岩,但其成因与蛇绿岩的演化密切相关。本文侵向于第二种可能性,认为新疆北部晚石炭-早二叠可能仍存在活动陆缘,俯冲作用仍然存在,扩张脊俯冲形成的板片窗效应导致地幔楔、俯冲板片和沉积物等熔融促使基性岩浆向长英质酸性岩浆转变,从而引发了二叠纪大规模玄武质岩浆底侵,导致了该时期的构造-岩浆-成矿-造山作用的发生。     

Petrology of the Tekirova (Antalya) ophiolite (Southern Turkey): evidence for diverse magma generations and their tectonic implications during Neotethyan-subduction

The SW Antalya Complex is an assemblage of Mesozoic carbonate platform, margin and ophiolitic rocks which record the formation and tectonic emplacement of a small Mesozoic ocean basin. The late Cretaceous ophiolitic rocks are located at two localities, namely the relatively intact Tekirova ophiolite to the east of Kemer zone and the dismembered Gödene ophiolite to the west of Kemer zone. The Tekirova (Antalya) ophiolite comprises harzburgitic tectonites, ultramafic to mafic cumulates, isotropic gabbros and sheeted dikes. Numerous isolated dikes, ranging in thickness from 5 cm to 10 m, intruded the crustal rocks at different structural levels. The isotropic gabbros are represented by gabbro, diorite and quartz diorite rocks with granular to ophitic–subophitic textures. The isolated dikes are characterized by dolerite, diabase and microdiorite with ophitic, intersertal and microgranular textures. These rocks exhibit tholeiitic to alkaline compositions. New geochemical data presented in this paper from the isolated dikes and isotropic gabbros suggest that there are three main types of parental basic magmas that form the oceanic crustal rocks of the Tekirova (Antalya) ophiolite. These are (1) IAT series which can be referred to the Group I isolated dikes and isotropic gabbros; (2) low-Ti boninitic series characterized by the Group II isolated dike and isotropic gabbros; and (3) OIB-type including the Group III isotropic gabbros. The geochemical evidence suggests that the crustal rocks of the Tekirova (Antalya) ophiolite were generated from a progressive source depletion from island arc tholeiites (IAT) to boninites. Therefore, a fore-arc tectonic setting seems likely for the generation of the crustal rocks from the Tekirova (Antalya) ophiolite in the southern branch of Neotethys during the Late Cretaceous. The OIB-type alkaline isotropic gabbros are thought to have resulted from either (1) a late-stage magmatic activity fed by melts that originated within an asthenospheric window due to slab break-off or (2) subduction of a ridge system which generated OIB source across the asthenospheric window that has been no influence of fluids from the subducted slab into the overlying mantle wedge, shortly before the emplacement of the Tekirova (Antalya) ophiolite onto the Tauride platform.     

Chemical exchange during hydrothermal alteration of basalt by seawater—II. Experimental results for Fe,Mn, and sulfur species

Fresh mid-ocean ridge basalts of varying crystallinity and an andesite were reacted with seawater and with a Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. $\text{Water}\text{rock}$ mass ratios of one to three were used and durations ranged from two to twenty months. The concentrations of Fe, Mn, and reduced and oxidized sulfur species in solution reached steady state in most of the experiments at 400–500°C, but not in those at 200–300°. The concentrations of Fe and Mn were a few ppm at 200–300° and increased greatly with temperature between 300 and 500°. The low values at 200–300° are probably related to the uptake of Fe and Mn by smectite at the in situ pH, which was slightly acid at 200° and slightly alkaline at 300°. The quench pH values decreased with increasing temperature above 300°. The only reliable data for the concentration of Zn in solution were obtained at 400°, where values 1–2 ppm were found. Copper was extensively leached from basalt and andesite and was deposited as part of a Cu-Au alloy in the capsule walls or, in some experiments, as chalcopyrite.Reduced sulfur was readily leached from basalt into solution, and was also produced by the reduction of seawater sulfate by ferrous iron derived from the basalts. The proportion of seawater sulfate which was reduced in the experiments with a $\text{water}\text{rock}$ ratio of one varied from 5–10% at 300°C to > 95% at 500°. The rate of sulfate reduction depended on the run temperature, on the crystallinity and initial sulfur content of the rocks used as starting materials, and on the $\text{water}\text{rock}$ ratio. The final concentration of reduced sulfur in solution increased greatly with temperature, and generally exceeded that of Fe on a molal basis.The oxide-sulfide assemblages produced in the experiments resemble those in the basalt-seawater geothermal system at Reykjanes, Iceland, and in hydrothermally altered basalts and gabbros from the oceanic crust; they include pyrite, pyrrhotite. chalcopyrite, hematite, and probably magnetite. The particular assemblage varied systematically with the temperature, rock type, and crystallinity of each run. Anhydrite precipitated in all experiments with seawater, at all temperatures from 200–500°C. However, its persistence to the end of the runs was apparently metastable, as it should have reacted with the final solutions to produce pyrite or pyrrhotite.     

Low temperature basalt alteration by sea water: an experimental study at 70°C and 150°C

Basaltic glass and diabase were reacted with seawater at 70°C at 1 bar and 150°C at 500 bars to determine fluid composition and alteration mineralogy. All experiments were performed at a water/ rock mass ratio of 10.The changes in seawater chemistry depended on temperature and crystallinity of the basalt. The experiment at 70°C produced a slight but continuous loss of Mg, Na and K and enrichment of Ca and SiO₂ in the seawater while pH decreased slowly. At 150°C, in contrast, Mg and SO₄ were quickly and quantitatively removed while Ca, SiO₂, Na, K, Fe, Mn and Ba were added to the seawater. pH rose to values between 5.5 and 6.5 after an initial drop to lower values. Basalt glass reacted more extensively at 150°C than diabase.Smectite was the major alteration product (iron-rich saponite) at 150°C for both the glass and diabase experiments. Smectite from the diabase experiment was well crystallized while that from the glass experiment was poorly crystallized. The smectites are similar to smectites found in altered oceanic ophiolitic basalts.     

西藏永珠——果芒错蛇绿岩的地球化学特征及其构造意义

永珠-果芒错蛇绿岩位于西藏永珠藏布-纳木错蛇绿岩带西段,主要由变质橄榄岩、辉长辉绿岩及玄武岩等组成。变质橄榄岩以富Mg,贫Ti、∑REE为特征。辉绿岩和玄武岩的主量元素、微量元素分析显示其含有洋脊拉斑玄武岩和岛弧拉斑玄武岩的双重成分特征,其中高场强元素（Nb、Ta、Zr、Hf等）亏损,大离子亲石元素（Rb、Sr、Ba等）相对富集,具有岛弧玄武岩的特点;在球粒陨石标准化稀土元素配分模式图上显示稀土元素特征为LREE亏损的平坦型,无负Eu异常,与洋中脊玄武岩的特征类似。通过与典型地区作对比和应用构造环境判别图解,推断永珠-果芒错蛇绿岩形成于弧后盆地的构造环境。     

The Macquarie Island ophiolite complex: Mid-Tertiary oceanic lithosphere from a major ocean basin

The rocks of Macquarie Island are part of the mid-Tertiary oceanic lithosphere from a major ocean basin. They were probably created at the Indian—Australian—Pacific spreading ridge.The basalts and dolerites are usually porphyritic, carry plagioclase (An_87-80) as a dominant phenocryst phase with less abundant olivine (Fo_89-85), chrome spinel and rare clinopyroxene (Ca₄₅Mg₅₀Fe₅|Ca₃₈Mg₅₀Fe₁₂) phenocrysts. Normatively the rocks range from ne- to Q-bearing, with most falling near the critical plane of normative silica undersaturation. Dykes tend to be more Fe-rich than lavas, and to include the more di-poor rocks. The rocks also range compositionally from typical ocean floor basalts through to varieties relatively enriched in some incompatible trace elements, particularly Nb (20–60 ppm), that otherwise retain ocean-floor basalt phenocryst assemblages, major-element compositions and Ti, Ni, Cr and Zr contents. This enrichment, also characteristic of ocean-floor basalts from the “abnormal” ridge segments near 45° N and 36° N (FAMOUS area) on the Mid-Atlantic Ridge, causes the rocks to plot away from the ocean-floor basalt fields on popular trace-element diagrams intended to identify tectonic affinities of basalts.The upper parts of the Macquarie Island oceanic lithosphere section can be thought of as a vertical slice through a magma column, differentiating at shallow levels. The layered and massive gabbros that underlie the basalts and dolerites are composed essentially of olivine, plagioclase and clinopyroxene. Olivine and plagioclase are cumulate phases in the layered rocks, clinopyroxene is postcumulus. Mineral compositions of the gabbros, particularly those of the layered rocks, are closely resembled by phenocryst compositions in the basalts and dolerites. Plagiogranites and trondheimites are unknown from the island, and norites very rare. Thus, Macquarie Island basalts, dolerites and gabbros form a distinctive igneous association that ought to make Macquarie Island-type ophiolite complexes from major ocean basins an easily recognized ophiolite type in continental orogenic terranes, even when dismembered.     

The trace element geochemistry of Corsican ophiolites

Ultramafic rocks, gabbros, plagiogranites, dolerites and basaltic dikes and pillows lavas of the ophiolite slices of eastern Corsica have been metamorphosed in both oceanic and orogenic environments. The trace element content of the metabasaltic rocks which exhibit a tholeiitic differentiation trend towards a ferrobasaltic composition, is similar to that of oceanic basalts. The cumulate sequence is interpreted to have been formed by fractional crystallization from an olivine-tholeiite magma. The troctolites representing cumulates derived from melts representing liquid fractions in the range F=1-0.85, gabbros from melts with F=0.85-0.45, and ferrogabbros and plagiogranites from melts with F<0.45. An oceanic environment with moderate spreading rates and magmatic processes similar to present-day normal oceanic ridge segments is considered the more probable original setting of the Corsican ophiolites.Financial support by C.N.R. (Italy) and A.T.P. Géodynamique de la Méditerranée Occidentale C.N.R.S. (France)     

西藏泽当—罗布莎蛇绿岩的地球化学特征及其构造意义

西藏泽当—罗布莎蛇绿岩是雅鲁藏布江蛇绿岩带的重要组成部分,受控于板块碰撞结合带。该蛇绿岩主要由变质橄榄岩、辉长辉绿岩及玄武岩等组成。变质橄榄岩具有低的A l2O3和CaO含量,以富Mg,贫Ti、∑REE为特征,与世界上典型蛇绿岩中方辉橄榄岩的特征值一致。辉长岩和玄武岩的主量元素、微量元素特征显示其含有洋脊拉斑玄武岩和大洋岛弧拉斑玄武岩的双重成分,其中高场强元素Nb、Ta、Zr、H f等亏损,大离子亲石元素Rb、Sr、Ba等相对富集,具有大洋岛弧玄武岩的特点。辉长岩在球粒陨石标准化稀土元素配分模式图上为LREE亏损的平坦型,无负Eu异常,与洋中脊玄武岩类似。根据上述特征并结合区域地质构造特征,认为泽当?罗布莎蛇绿岩可能形成于边缘海盆地的海底慢速扩张环境。     

Petrology,geochemistry and geochronology of the Zhongcang ophiolite,northern Tibet: implications for the evolution of the Bangong-Nujiang Ocean

Ophiolites are widespread along the Bangong-Nujiang suture zone, northern Tibet. However, it is still debated on the formation ages and tectonic evolution process of these ophiolites. The Zhongcang ophiolite is a typical ophiolite in the western part of the Bangong-Nujiang suture zone. It is composed of serpentinized peridotite, cumulate and isotropic gabbros, massive and pillow basalts, basaltic volcanic breccia, and minor red chert. Zircon SHRIMP Ue Pb dating for the isotropic gabbro yielded weighted mean age of 163.4 ± 1.8 Ma. Positive zircon ε Hf(t) values(+15.0 to +20.2) and mantle-like σ~(18)O values(5.29 ±0.21)% indicate that the isotropic gabbros were derived from a long-term depleted mantle source. The isotropic gabbros have normal mid-ocean ridge basalt(N-MORB) like immobile element patterns with high Mg O, low TiO_2 and moderate rare earth element(REE) abundances, and negative Nb,Ti, Zr and Hf anomalies. Basalts show typical oceanic island basalt(OIB) geochemical features, and they are similar to those of OIB-type rocks of the Early Cretaceous Zhongcang oceanic plateau within the Bangong-Nujiang Ocean. Together with these data, we suggest that the Zhongcang ophiolite was probably formed by the subduction of the Bangong-Nujiang Ocean during the Middle Jurassic. The subduction of the Bangong-Nujiang Tethyan Ocean could begin in the Earlye Middle Jurassic and continue to the Early Cretaceous, and finally continental collision between the Lhasa and Qiangtang terranes at the west Bangong-Nujiang suture zone probably has taken place later than the Early Cretaceous(ca. 110 Ma).     

Mg-metasomatism of oceanic gabbros and its control on Ti-clinohumite formation during eclogitization

In the high-pressure meta-ophiolites of Western Liguria (Italy), serpentinized ultramafites host bodies of eclogite, metarodingite and Ti-clinohumite ± Ti-chondrodite-bearing rocks. The latter contain relics of augite, ilmenite and apatite, which suggest derivation from pristine Fe-Ti-rich gabbros. The composition of relict mantle clinopyroxene in the host serpentinites indicates primary depleted peridotite compositions. Compared with their inferred protoliths, the Ti-clinohumite dikelets and the host serpentinites display significant changes in their major and trace element concentrations, indicating element exchange between the two rock systems. In particular, the Fe-Ti-rich gabbros were depleted in CaO and FeO and were strongly enriched in MgO. Analogous compositional variations are shown by altered gabbros enclosed in serpentinized peridotites from the obducted ophiolite sequences of the Northern Apennine. This evidence suggests that the observed Mg-enrichment recorded by the Ti-clinohumite metagabbros occurred in oceanic environments as the result of diffusive exchange between ultramafites and gabbros in presence of fluids related to serpentinization of the ultramafic country rocks. Alteration of the gabbro and concomitant Mg-uptake mostly caused extensive chloritization of the igneous plagioclase. Survival of igneous ilmenite and augite and their reaction with the hydrothermal chlorite during high-pressure metamorphism produced the observed Ti-clinohumite and Ti-chondrodite assemblages. The data presented thus indicate that crystallization of Ti-clinohumite assemblages was facilitated by a stage of oceanic alteration leading to Mg-enrichment of original Fe-Ti-rich gabbros. We suggest that during alteration, Mg-metasomatism occurred prior to rodingitization and was related to the earlier stages of peridotite serpentinization. Survival of oceanic chemical heterogeneities in the Ti-clinohumite rocks, indicates that element mobility during high-pressure recrystallization of these rocks was on a limited scale. This allowed preservation of their pre-subduction alteration features. Received: 13 July 1998 / Accepted: 3 November 1998     

Origin of the Xigaze ophiolite, Yarlung Zangbo suture zone, southern Tibet

The Xigaze ophiolite, (Tibet) displays unusual lithological, petrological, textural, and structural characteristics. There are no large masses of cumulate gabbros, but dolerite intrusives throughout the whole ophiolite sequence, some of which were intruded into already serpentinized peridotites, only minor residual harzburgites and dunites in dominantly Iherzolitic peridotites equilibrated at low temperatures and pressures, and relatively low-temperature deformation structures in the uppermost peridotites. These features suggest a very low heat flow at the spreading center where the Xigaze ophiolite was formed, in good agreement with a discontinuous and slowly-accreting spreading center origin. However, this ophiolite does not represent a typical mid-oceanic ridge ophiolite; rather it was formed in a small basin located at the southern margin of Eurasia, hence within a preexisting oceanic lithosphere. The opening of the nearly N-S Xigaze paleo-ridge resulted from the W-E drift of Africa relative to Eurasia from 180 to 110 Ma. The N-S emplacement onto the continent of the Xigaze ophiolite, formed 120 to 110 Ma ago, can be correlated to changes in direction of motion of the African and Indian plates: a primary intra-oceanic thrusting event probably occurring at 110 or 85 Ma and the final obduction near 50 Ma during the India-Eurasia collision.     

Hydrothermal alteration vs. ocean-floor metamorphism. A comparison between two case histories: the TAG hydrothermal mound (Mid-Atlantic Ridge) vs. DSDP/ODP Hole 504B (Equatorial East Pacific)

This article presents a review of hydrothermal alteration of the various basaltic rocks forming the oceanic crust, emphasizing especially on the water–rock interaction processes, the petrography and secondary mineralogy of hydrothermally altered rocks from the present-day ocean, hence excluding the ophiolitic complexes. A brief summary of the history of the first studies of hydrothermally altered oceanic rocks leads to a comparison between Miyashiro's concept of ‘ocean-floor metamorphism’ and that of hydrothermal alteration that warrant caution when applying Eskola's metamorphic facies of regional metamorphism to hydrothermally altered oceanic rocks. The functioning of mid-oceanic ridge axial hydrothermal systems, and the role of oceanic Layer-3 gabbros are discussed in detail. The mechanisms of the various alteration processes of the rocks forming the oceanic crust are presented. The case histories of the two examples more particularly studied by the author and his collaborators, are compared, i.e., the DSDP-ODP Hole 504B reference section South of the Costa Rica Ridge, and the TAG active mound at the Mid-Atlantic Ridge. The significance of the paragonitic phyllosilicate in highly altered rocks form the TAG Mound is compared to the other known occurrences of ‘white micas’ in the oceanic crust. The importance of metabasites as major components of the oceanic crust is emphasized. The elemental fluxes resulting from hydrothermal alteration of oceanic rocks in regulating seawater chemistry are only briefly alluded, because this topic is covered by the last article of this thematic issue by J.C. Alt, who assesses the chemical budgets resulting from ocean hydrothermal activity. To cite this article: J. Honnorez, C. R. Geoscience 335 (2003).