Antigorite-ophicarbonates: Contact metamorphism in Valmalenco,Italy

Outside the Bergell tonalite contact aureole, ophicarbonate rocks consist of blocks of antigorite schist embedded in veins of calcite ± tremolite. An antigorite schistosity predates some of these calcite veins. Mono- and bimineralic assemblages occur in reaction zones associated with the veins. Within the aureole, the ophicarbonate veining becomes less distinct and polymineralic assemblages become more frequent. A regular sequence of isobaric univariant assemblages is found, separated by isograds corresponding to isobaric invariant assemblages. In order of increasing grade the invariant assemblages are: antigorite+diopside+olivine+tremolite+calcite antigorite+dolomite+olivine+tremolite+calcite antigorite+olivine+talc+magnesite antigorite+dolomite+olivine+tremolite+talc These assemblages match a previously derived topology in P-T-X_CO2 space for the system CaO-MgO-SiO₂-H₂O-CO₂; the field sequence can be used to adjust the relative locations of calculated invariant points with respect to temperature. Isobaric univariant and invariant assemblages are plotted along a profile map to permit direct comparison with the phase diagram.It is inferred that, during the formation of the ophicarbonate veins, calcite precipitated from fluid introduced into the serpentinite. During contact metamorphism, however, the compositions of pore fluids evolved by reaction in the ophicarbonate rocks were largely buffered by the solid phases. This control occurred on a small scale, because there are local variations in the buffering solid assemblages within a centimeter range.     

High pressure breakdown of antigorite to spinifex-textured olivine and orthopyroxene, SE Spain

The prograde, high pressure, transition from antigorite serpentinite to enstatite-olivine rock occurs along a tectonically undisturbed profile at Cerro del Almirez, SE Spain. The reactant assemblage is antigorite + olivine with tremolite rimming precursor diopside. The product assemblage of tremolite + chlorite + enstatite + olivine has a spinifex-like texture with arborescent or radiating olivine elongated parallel to [001] and with radially grown enstatite. Product enstatite is very poor in Al₂O₃. Due to numerous oriented submicroscopic inclusions of chromian magnetite, product olivine has a brownish pleochroism and a bulk chromium content similar to precursor antigorite. Titanian clinohumite with a fluorine content of 0.45–0.50 wt% persisted beyond the breakdown of antigorite. The partitioning of iron and magnesium amongst the silicate phases is almost identical to that at lower pressures. Average K_d values Mn/Mg and Ni/Mg are 0.17 and 0.70 for antigorite-olivine pairs and 1.83 and 0.22 for orthopyroxene-olivine pairs, respectively. These data are useful in discriminating generations of olivine grown on each other. From the field data a phase diagram topology for a portion of the system CaO-MgO-SiO₂-H₂O is derived. This topology forms the basis for extrapolations into inaccessible P-T regions. Received: 6 February 1998 / Accepted: 24 March 1998     

Serpentinites of the Zermatt-Saas ophiolite complex and their texture evolution

The Zermatt‐Saas serpentinite complex is an integral member of the Penninic ophiolites of the Central Alps and represents the mantle part of the oceanic lithosphere of the Tethys. Metamorphic textures of the serpentinite preserve the complex mineralogical evolution from primary abyssal peridotite through ocean‐floor hydration, subduction‐related high‐pressure overprint, meso‐Alpine greenschist facies metamorphism, and late‐stage hydrothermal alteration. The early ocean floor hydration of the spinel harzburgites is still visible in relic pseudomorphic bastite and locally preserved mesh textures. The primary serpentine minerals were completely replaced by antigorite. The stable assemblage in subduction‐related mylonitic serpentinites is antigorite–olivine–magnetite ± diopside. The mid‐Tertiary greenschist facies overprint is characterized by minor antigorite recrystallization. Textural and mineral composition data of this study prove that the hydrated mineral assemblages remained stable during high‐pressure metamorphism of up to 2.5 GPa and 650 °C. The Zermatt‐Saas serpentinites thus provide a well documented example for the lack of dehydration of a mantle fragment during subduction to 75 km depth.     

Serpentinization history of the Río Guanajibo serpentinite body,Puerto Rico

The Río Guanajibo serpentinite body (RGSB) near Mayagüez, Puerto Rico, is part of an ophiolite mélange thrust in an oceanic convergent zone. The aim of this study was to characterize the extent and chronology of serpentinization within this peridotite mass. Mineralogy, microstructures, and veining episodes within the RGSB were characterized using optical microscopy, x-ray diffraction (XRD), scanning electron microscopy (SEM), and structural analyses. This study identified, for the first time, all three serpentine polymorphs (i.e., antigorite, chrysotile, lizardite) in serpentinite samples collected from Puerto Rico. Lizardite, the initial serpentine mineral formed from widespread hydration of olivine, was found throughout serpentinite samples. Chrysotile was the most abundant polymorph observed in sheared serpentinite samples, consistent with conditions favoring low fluid to rock ratios, supersaturation and abundant porosity. Antigorite was observed as a replacement texture in serpentinites that were not exposed to greenschist facies metamorphic conditions, and were frequently found in veins with a shear component. The results indicate that metamorphic conditions do not exclusively dictate polymorph formation.The mineralogy and textures observed within the different vein generations reflect the formation conditions, and deformational mechanisms, that occurred during the serpentinization process; six veining episodes (V1 – V6) were identified and grouped into four stages of serpentinization. Stage one (V1 and V2 type veins) represents the earliest stages of serpentinization and was characterized by microscopic fracture networks that formed as a result of cracking during the initial hydration of olivine under low water/rock ratios. During stage two (V3 and V4 type veins), fibrous crack - seal veins formed to accommodate continued volume expansion, via incremental fracture openings, caused by continued hydration of olivine. The ascension of serpentinite into the upper lithosphere was inferred to occur during Stage three; V5 type veins are associated with this stage. Textures and vein morphologies, representing supersaturated conditions and a decrease in temperature, were observed. Stage 4 (V6 type veins) was characterized by shear deformation features, which formed as a result of thrusting associated with the emplacement of the RGSB or Late Eocene transpression and fault reactivation along the Caribbean plate boundary.     

Three steps of serpentinization in an eclogitized oceanic serpentinization front (Lanzo Massif – Western Alps)

The Lanzo peridotite massif is a fragment of oceanic lithosphere generated in an ocean–continent transition context and eclogitized during alpine collision. Despite the subduction history, the massif has preserved its sedimentary oceanic cover, suggesting that it may have preserved its oceanic structure. It is an exceptional case for studying the evolution of a fragment of the lithosphere from its oceanization to its subduction and then exhumation. We present a field and petrological study retracing the different serpentinization episodes and their impact on the massif structure. The Lanzo massif is composed of slightly serpentinized peridotites (<20% serpentinization) surrounded by an envelope of foliated serpentinites (100% serpentinization) bordered by oceanic metabasalts and metasedimentary rocks. The limit between peridotites and serpentinites defines the front of serpentinization. This limit is sharp: it is marked by the presence of massive serpentinites (80% serpentinization) and, locally, by dykes of metagabbros and mylonitic gabbros. The deformation of these gabbros is contemporaneous with the emplacement of the magma. The presence of early lizardite in the peridotites testifies that serpentinization began during the oceanization, which is confirmed by the presence of meta‐ophicarbonates bordering the foliated serpentinite envelope. Two additional generations of serpentine occur in the ultramafic rocks. The first is a prograde antigorite that partially replaced the lizardite and the relict primary minerals of the peridotite during subduction, indicating that serpentinization is an active process at the ridge and in the subduction zone. Locally, this episode is followed by the deserpentinization of antigorite at peak P–T (estimated in eclogitized metagabbros at 2–2.5 GPa and 550–620 °C): it is marked by the crystallization of secondary olivine associated with chlorite and/or antigorite and of clinopyroxene, amphibole and chlorite assemblages. A second antigorite formed during exhumation partially to completely obliterating previous textures in the massive and foliated serpentinites. Serpentinites are an important component of the oceanic lithosphere generated in slow to ultraslow spreading settings, and in these settings, there is a serpentinization gradient with depth in the upper mantle. The seismic Moho limit could correspond to a serpentinization front affecting the mantle. This partially serpentinized zone constitutes a less competent level where, during subduction and exhumation, deformation and fluid circulation are localized. In this zone, the reaction kinetics are increased and the later steps of serpentinization obliterate the evidence of this progressive zone of serpentinization. In the Lanzo massif, this zone fully recrystallized into serpentinite during alpine subduction and collision. Thus, the serpentinite envelope represents the oceanic crust as defined by geophysicists, and the sharp front of serpentinization corresponds to an eclogitized seismic palaeo‐Moho.     

Trace-element geochemistry of transform-fault serpentinite in high-pressure subduction mélanges (eastern Cuba): implications for subduction initiation

The Sierra del Convento and La Corea mélanges (eastern Cuba) are vestiges of a Cretaceous subduction channel in the Caribbean realm. Both mélanges contain blocks of oceanic crust and serpentinite subducted to high pressure within a serpentinite matrix. The bulk composition of serpentinite indicates spinel-harzburgite and -herzolite protoliths. The samples preserve fertile protolith signatures that suggest low melting degrees. High concentration of immobile elements Zr, Th, Nb, and REE contents (from ~0.1 to ~2 CI-chondrite) point to early melt–rock interaction processes before serpentinization took place. Major- and trace-element compositions suggest an oceanic fracture-zone–transform-fault setting. A mild negative Eu anomaly in most samples indicates low-temperature fluid–rock interaction as a likely consequence of seawater infiltration during oceanic serpentinization. A second, more important, serpentinization stage is related to enrichment in U, Pb, Cs, Ba, and Sr due to the infiltration of slab-derived fluids. The mineral assemblages are mainly formed by antigorite, lizardite, and chlorite, with local minor talc, tremolite, anthophyllite, dolomite, brucite, and relict orthopyroxene. The local presence of anthophyllite and the replacements of lizardite by antigorite indicate a metamorphic evolution from the cooling of peridotite/serpentinite at the oceanic context to mild heating and compression in a subduction setting. We propose that serpentinites formed at an oceanic transform-fault setting that was the locus of subduction initiation of the Proto-Caribbean basin below the Caribbean plate during early Cretaceous times. Onset of subduction at the fracture zone allowed the preservation of abyssal transform-fault serpentinites at the upper plate, whereas limited downward drag during mature subduction placed the rocks in the subduction channel where they tectonically mixed with the upward-migrating accreted block of the subducted Proto-Caribbean oceanic crust. Hence, we suggest that relatively fertile serpentinites of high-pressure mélanges were witness to the onset of subduction at an oceanic transform-fault setting.     

俯冲带蛇纹岩的变质过程

俯冲带蛇纹岩是俯冲带流体的重要来源,特别是其深部脱水作用对地幔动力学影响深远,是研究俯冲带约80~200km深度范围的地球动力学的关键,因此研究蛇纹岩的变质作用过程及其相关特征矿物(组合)的温压稳定范围具有重要意义。蛇纹岩具有简单的矿物(组合):蛇纹石类、硅镁石类、磁铁矿、氢氧镁石、绿泥石、橄榄石、透辉石、角闪石、滑石等,并且这些矿物(组合)对温压变化不敏感从而很难用来判定蛇纹岩所经历的变质演化轨迹。近几十年来,研究者通过实验岩石学和野外地质观察,主要研究了蛇纹石类矿物和硅镁石类矿物的温压稳定范围,并且试图使用这些特征矿物(组合)来判定俯冲带蛇纹岩的峰期变质条件。本文总结了蛇纹岩中这些主要矿物的温压稳定范围和相关变质反应,并且以中国西南天山蛇纹岩为例,展示使用特征矿物(组合)和叶蛇纹石Al等值线判定蛇纹岩峰期温压条件在实际岩石中的应用。另外,早期对叶蛇纹石的研究表明:随着温压条件的变化,叶蛇纹石的晶体结构会发生相应的调整。表现为单位晶胞内硅氧四面体的个数(m值)发生变化:温度升高,m值变小;压力升高,m值变大,这个发现在高压实验和天然样品中得到了一定程度的验证。本文利用已知峰期温压范围的叶蛇纹石样品分别采用粉末制样法和离子减薄制样法,进行透射电镜测试(TEM)样品的m值,并通过统计的方法获得叶蛇纹石的m值的峰值。结果显示叶蛇纹石的m值的峰值在一定程度上可以用以指示温压条件。本文提出可以用矿物组合、叶蛇纹石Al等值线和叶蛇纹石m值峰值相结合的方法确定蛇纹岩的变质温压条件和P-T轨迹。     

Serpentinization: a review

The common alteration assemblage produced by serpentinization of ultramafic rocks is: lizardite, chrysotile, magnetite±brucite±antigorite. Lizardite-chrysotile serpentinites are more common than antigorite; the presence of antigorite indicates that the serpentinite has undergone prograde metamorphism or that the periootite was serpentinized in a higher P,T regime than lizardite and chrysotile. The iron subsitution into serpentine minerals and brucite is a function of temperature at low f_O2, with increased temperature enhancing magnetite formation. The presence of awaruite and native Fe are strong evidence for a locally very reducing environment. Isotopic studies have shown a wide variety of origins for the fluids involved in serpentinization. The increased boron content of serpentinized rocks when compared to boron contents of the parent ultramafic body indicates a possible sea water origin for the fluids. Serpentinization takes place under both constant volume and constant chemical composition conditions. The factors in evaluating the importance of the two processes for an individual serpentinite are: (1) determination of the mineral assemblage and its paragenesis, (2) the structural and tectonic relationship of the ultramafic body to its country rock, (3) fluid access to the rock in duration and amount, and (4) timing of serpentinization - before, during or after emplacement into the crust.     

Subduction metamorphism of serpentinite‐hosted carbonates beyond antigorite‐serpentinite dehydration (Nevado‐Filábride Complex,Spain)

At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO₂ contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO₂ ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H₂O–CO₂ fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H₂O and molecular CO₂ are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H₂O–CO₂ fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle.     

Mantle peridotite in newly discovered far-inland subduction complex,southwest Arizona: initial report

The latest Cretaceous to early Palaeogene Orocopia Schist and related units are generally considered a low-angle subduction complex that underlies much of southern California and Arizona. A recently discovered exposure of Orocopia Schist at Cemetery Ridge west of Phoenix, Arizona, lies exceptionally far inland from the continental margin. Unexpectedly, this body of Orocopia Schist contains numerous blocks, as large as ~300 m, of variably serpentinized mantle peridotite. These are unique; elsewhere in the Orocopia and related schists, peridotite is rare and completely serpentinized. Peridotite and metaperidotite at Cemetery Ridge are of three principal types: (1) serpentinite and tremolite serpentinite, derived from dunite; (2) partially serpentinized harzburgite and olivine orthopyroxenite (collectively, harzburgite); and (3) granoblastic or schistose metasomatic rocks, derived from serpentinite, made largely of actinolite, calcic plagioclase, hercynite, and chlorite. In the serpentinite, paucity of relict olivine, relatively abundant magnetite (5%), and elevated Fe³⁺/Fe indicate advanced serpentinization. Harzburgite contains abundant orthopyroxene, only slightly serpentinized, and minor to moderate (1–15%) relict olivine. Mantle tectonite fabric is locally preserved. Several petrographic and geochemical characteristics of the peridotite at Cemetery Ridge are ambiguously similar to either abyssal or mantle-wedge (suprasubduction) peridotites and serpentinites. Least ambiguous are orthopyroxene compositions. Orthopyroxene is distinctively depleted in Al₂O₃, Cr₂O₃, and CaO, indicating mantle-wedge affinities. Initial interpretation of field and petrologic data suggests that the peridotite blocks in the Orocopia Schist subduction complex at Cemetery Ridge may be derived from the leading corner or edge of a mantle wedge, presumably in (pre-San Andreas fault) southwest California. However, derivation from a subducting plate is not precluded.     

Small-scale mélange fabric between serpentinite block and matrix: Magnetic evidence from the Mitsuishi ultramafic rock body, Hokkaido, Japan

The Mitsuishi ultramafic rock body in Hokkaido, Japan, consists mainly of serpentinized peridotites that originated from a depleted mantle. This study aims to show new evidence of small-scale mélange fabric of serpentinite matrix in the rock body. Each serpentinite block in the serpentine matrix shows large and stable intensities of natural remanent magnetization (NRM). However, the directions of serpentinite blocks' NRM in the matrix are randomly scattered. A Curie temperature (Tc) of 580 °C corresponding to pure magnetite was also observed. Additionally, there is no evidence of heating over 580 °C after serpentinization. The blocks in the matrix must have obtained crystallization remanent magnetization (CRM) during serpentinization. The directions of the blocks' characteristic remanent magnetization (ChRM) are also scattered. It shows that serpentinite blocks were magnetized prior to uplifting. The results of the study indicate that the magnetic carrier of the serpentinite blocks in the matrix is mainly composed of magnetite, and it can keep original magnetization before uplifting. The results also imply that the scattering directions of NRM indicate the presence of small-scale mélange fabric of serpentinite matrix.     

The role of fluids in the metamorphism of komatiites,Agnew nickel deposit,western Australia

The Agnew nickel sulfide deposit is spatially associated with a lenticular body of ultramafic rocks which shows a concentric zonation in metamorphic mineralogy. Olivine + tremolite + chlorite + cummingtonite ±enstatite assemblages occur at the margin of the ultramafic lens, giving way to olivine + anthophyllite, olivine + talc and olivine + antigorite assemblages successively inwards. These rocks are interpreted as having crystallized from komatiitic lavas, and exhibit a spectrum of compositions from those of original flow tops to pure olivine adcumulates. The relative modal abundances of metamorphic olivine, tremolite and chlorite reflect original proportions of cumulus olivine and komatiite liquid in the protolith. Peak metamorphic conditions are estimated at 550° C, based on garnet-biotite thermometry, at a maximum pressure of 3 kb. This temperature falls within the narrow range over which metamorphic olivine may co-exist with enstatite, anthophyllite, talc or antigorite depending upon the fugacity of water in the metamorphic fluid. The observed mineralogical zonation is therefore attributed to infiltration by CO₂-rich fluids, generated by decarbonation of talc-carbonate rocks formed during pre-metamorphic marginal alteration of the ultramafic lens. Metamorphic fluids were essentially binary mixtures of water and CO₂, with minor H₂S having a maximum partial pressure less than 1 percent of total pressure. Enstatite-bearing assemblages formed in the presence of CO₂-rich fluids at fluid: rock volume ratios close to one, while anthophyllite, talc and antigorite bearing assemblages formed in the presence of progressively more water-rich fluids at progressively lower fluid-rock ratios.     

Eclogite facies metarodingites – phase relations in the system SiO2-Al2O3-Fe2O3-FeO-MgO-CaO-CO2-H2O: an example from the Zermatt-Saas ophiolite

Eclogite facies metarodingites occur as deformed dykes in serpentinites of the Zermatt‐Saas ophiolite (Western Alps). They formed during the subduction of the Tethys oceanic lithosphere in the Early Tertiary. The metarodingites developed as a consequence of serpentinization of the oceanic mantle. Three major types of metarodingites (R1, R2 & R3) can be distinguished on the basis of their mineralogical composition. All metarodingites contain vesuvianite, chlorite and hydrogrossular in high modal amounts. In addition they contain: R1 – diopside, tremolite, clinozoisite, calcite; R2 – hydroandradite, diopside, epidote, calcite; and R3 – hydroandradite. Both garnets contain a small but persistent amount of hydrogarnet component. The different metarodingites reflect different original dyke rocks in the mantle. In each group of metarodingite, textural relations suggest that reactions adjusted the assemblages along the P–T path travelled by the ophiolite during subduction and exhumation. Reactions and phase relations derived from local textures in metarodingite can be modelled in the eight‐component system: SiO₂‐Al₂O₃‐Fe₂O₃‐FeO‐MgO‐CaO‐CO₂‐H₂O. This permits the analysis of redox reactions in the presence of andradite garnet and epidote in many of the rocks. Within this system, the phase relations in eclogite facies metarodingites have been explored in terms of T–X_CO2, T–μ(SiO₂), μ(Cal)–μ(SiO₂) and P–T sections. It was found that rodingite assemblages are characterized by low μ(SiO₂) and low X_CO2 conditions. The low SiO₂ potential is externally imposed onto the rodingites by the large volume of antigorite‐forsterite serpentinites enclosing them. Moreover, μ(SiO₂) decreases consistently from metarodingite R1 to R3. The low μ(SiO₂) enforced by the serpentinites favours the formation of hydrogarnet and vesuvianite. Rodingite formation is commonly associated with hydrothermal alteration of oceanic lithosphere at the ocean floor, in particular to ocean floor serpentinization. Our analysis, however, suggests that the metarodingite assemblages may have formed at high‐pressure conditions in the subduction zone as a result of serpentinization of oceanic mantle by subduction zone fluids.     

An experimental investigation of antigorite dehydration in natural silica-enriched serpentinite

Piston cylinder experiments were performed to constrain the pressure and temperature conditions for two high-pressure antigorite dehydration reactions found in silica-enriched serpentinites from Cerro del Almirez (Nevado–Filábride Complex, Betic Cordillera, southern Spain). At 630–660°C and pressures greater than 1.6 GPa, antigorite first reacts with talc to form orthopyroxene ± chlorite + fluid. We show that orthopyroxene + antigorite is restricted to high-pressure metamorphism of silica-enriched serpentinite. This uncommon assemblage is helpful in constraining metamorphic conditions in cold subduction environments, where antigorite serpentinites have no diagnostic assemblages over a large pressure and temperature range. The second dehydration reaction leads to the breakdown of antigorite to olivine + orthopyroxene + chlorite + fluid. The maximum stability of antigorite is found at 680°C at 1.9 GPa, which also corresponds to the maximum pressure limit for tremolite coexisting with olivine + orthopyroxene. The high aluminium (3.70 wt% Al₂O₃) and chromium contents (0.59 wt% Cr₂O₃) of antigorite in the investigated starting material is responsible for the expansion of the serpentinite stability to 60–70°C higher temperatures at 1.8 GPa than the antigorite stability calculated in the Al-free system. The antigorite from our study has the highest Al–Cr contents among all experimental studies and therefore likely constraints the maximum stability of antigorite in natural systems. Comparison of experimental results with olivine–orthopyroxene–chlorite–tremolite assemblages outcropping in Cerro del Almirez indicates that peak metamorphic conditions were 680–710°C and 1.6–1.9 GPa.     

大洋橄榄岩的蛇纹石化过程:从海底水化到俯冲脱水SCIEI北大核心CSCD

蛇纹石化是海底最重要的水岩相互作用之一,指基性岩和超基性岩中的橄榄石和辉石等镁铁质矿物在相对低温条件下发生水热蚀变产生蛇纹石等矿物的热液变质作用。蛇纹石族矿物主要有三种,分别是利蛇纹石、纤蛇纹石和叶蛇纹石。低温状态蛇纹石族矿物主要以利蛇纹石和纤蛇纹石的形式存在,高温状态下主要以叶蛇纹石的形式存在。影响大洋蛇纹石化过程的因素不容忽视,温度、氧化还原程度、pH值、水岩比(W/R)等都在其中扮演着重要的角色。总的来说,地幔物质易出露在地壳减薄区域和断裂构造处,这有利于与流体充分接触反应,从而决定了大洋蛇纹石化作用发生的可能位置。对蛇纹石化程度的描述,当前人们大多通过岩石微观结构、地球化学指标来定性指示,磁学指标有望实现对蛇纹石化程度的定量解释。蛇纹石化作用对海底磁异常、地球生命演化进程、成矿作用等都有一定的贡献。此外,俯冲带脱水及弧岩浆的形成都与之有联系。总之,基性与超基性岩石蛇纹石化与俯冲带蛇纹岩脱水过程是地球水循环过程的重要机制,但未来揭示蛇纹岩的磁学性质和俯冲变质过程,仍需进一步探索。     

Alpine olivine- and titanian clinohumite-bearing assemblages in the Erro-Tobbio peridotite (Voltri Massif, NW Italy)

The microstructures in the Erro-Tobbio peridotite indicate several stages of recrystallization of olivine + titanian clinohumite-bearing assemblages. The development of these assemblages is closely associated with serpentinite mylonites, in which they occur in shear bands and foliations and are inferred to have grown synkinematically, in veins, and as post-kinematic radial aggregates. In the peridotite wall-rock adjacent to these mylonites, the same assemblages have recrystallized statically at the expense of original olivine and pyroxenes, mesh-textured chrysolite and antigorite veins. In addition, the olivine-bearing assemblage occurs in widespread vein systems. The brittle deformation of the peridotite resulting in the development of these vein systems is closely related to ductile deformation of metagabbroic dykes in the peridotite. Although early metasomatism resulted in extensive rodingitization of the gabbros, some dykes show an eclogitic assemblage of Na-clinopyroxene + garnet + chloritoid + chlorite ± talc. These observations, the microstructures and the mineral chemistry all suggest that the assemblages in the ultramafic rocks and metagabbros developed during a prograde evolution towards high pressures (>13–16 kbar, 450–550° C), and during subsequent decompression. This metamorphic evolution is considered to be related to Late Cretaceous intraoceanic subduction in the Alps-Apennine system and closure of the Piedmont-Ligurian basin.     

Microstructural and fabric studies from the rocks of the Moine Nappe,Eriboll, NW Scotland

Microstructures and quartz c-axis fabric diagrams from mylonites and psammitic Moine schists, collected in traverses across the lower levels of the Moine Nappe in the Eriboll area, are presented. On approaching the Moine Thrust from the Kyle of Tongue, the following microstructural sequence is encountered: interlayered coarse grained biotite psammitic and schistose tectonites being in part mylonitic with two platy slide zones, one containing biotite and the other only muscovite and chlorite and both showing quartz microstructures indicative of post-tectonic relaxation; these pass into more mylonitic rocks nearer the thrust zone which in turn passes into the main chlorite-grade mylonite belt and finally, adjacent to the Moine Thrust, into reworked lower chlorite grade mylonites. Although there is some local variation, the overall quartz c-axis fabric is an incomplete asymmetric type I girdle. The main variation is the development of type II girdles in the reworked, ultrafine grained mylonites. The extent of the mylonitization is more extensive than previously reported. Studies of folds within the mylonite belt have revealed eye structures and small-scale folds; many are sheath folds. They cannot be unequivocally correlated with large-scale recumbent folds within the Moine Nappe. The results presented indicate that mylonitization is not limited to a single phase, and raises the possibility that there may be earlier Caledonian or possibly Precambrian structural elements present in the Eriboll region Moines prior to much of the mylonitization.     

蛇纹石化和俯冲带蛇纹岩变质脱水过程中流体活动性元素的行为

蛇纹石是大洋岩石圈和俯冲带内水和流体活动性元素最重要的载体之一。研究蛇纹石化和蛇纹岩变质脱水过程中流体活动性元素的行为是认识俯冲带元素地球化学循环的关键。蛇纹岩是指主要由蛇纹石类矿物构成的岩石,包括利蛇纹石、纤蛇纹石和叶蛇纹石。蛇纹石化过程中会造成流体活动性元素(B、Li、As、Sb、Pb、Cs、U、Sr和Ba等)的显著富集,并且由于原岩性质、流体成分和氧逸度等条件的不同,大洋岩石圈蛇纹岩和弧前蛇纹岩的特征也略有不同。例如,弧前蛇纹岩具有相对高的As、Sb、B和相对低的U,这反映了俯冲沉积物来源流体的贡献。在俯冲带蛇纹岩的变质脱水过程中,利蛇纹石向叶蛇纹石的转变伴随着矿物内超过50%F和Cl的释放,以及一些流体活动性元素(如B和Li)的迁出;此外,蛇纹石分解形成的变质橄榄石中的流体包裹体指示,蛇纹石脱水分解所产生的流体具有高于原始地幔几个数量级的Cl、Cs、Pb、As、Sb、Ba、Rb、B、Sr、Li和U含量。由于利蛇纹石中的Fe~(3+)含量较叶蛇纹石高,这种矿物相转变过程中也伴随着俯冲通道内的一系列氧化还原过程,从而影响流体性质和新形成的叶蛇纹石的成分。蛇纹岩与岛弧岩浆在流体活动性元素富集规律上的相似性说明蛇纹岩在俯冲带元素循环中扮演着重要的角色。此外,蛇纹石矿物相转变过程中F、Cl、B等元素的释放,可能对于斑岩型金矿、蛇绿岩中的金矿和某些蛇纹岩作为赋矿围岩的硼矿的形成起到重要的作用。     

On Silica Activity and Serpentinization

Serpentinites have the lowest silica activity of common crustalrocks. At the serpentinization front, where olivine, serpentine,and brucite are present, silica activities (relative to quartz)are of the order of 10^–2·5 to 10^–5, dependingon the temperature. Here we argue that this low silica activityis the critical property that produces the unusual geochemicalenvironments characteristic of serpentinization. The formationof magnetite is driven by the extraction of silica from theFe₃Si₂O₅(OH)₄ component of serpentine, producing extremely reducingconditions as evinced by the rare iron alloys that partiallyserpentinized peridotites contain. The incongruent dissolutionof diopside to form Ca²⁺, serpentine, and silica becomes increasinglyfavored at lower T, producing the alkalic fluids characteristicof serpentinites. The interaction of these fluids with adjacentrocks produces rodingites, and we argue that desilication isalso part of the rodingite-forming process. The low silica activityalso explains the occurrence of low-silica minerals such ashydrogrossular, andradite, jadeite, diaspore, and corundum inserpentinites or rocks adjacent to serpentinites. The tendencyfor silica activity to decrease with decreasing temperaturemeans that the presence of certain minerals in serpentinitescan be used as indicators of the temperature of serpentinization.These include, with decreasing temperature, diopside, andraditeand diaspore. Because the assemblage serpentine + brucite marksthe lowest silica activity reached in most serpentinites, thepresence and distribution of brucite, which commonly is a crypticphase in serpentinites, is critical to interpreting the processesthat lead to the hydration of any given serpentinite. KEY WORDS: serpentinization; serpentinites; silica activity; oxygen fugacity; rodingites; magnetization of serpentinites     

Petrology of titanian clinohumite and olivine at the high-pressure breakdown of antigorite serpentinite to chlorite harzburgite (Almirez Massif,S. Spain)

Rocks of the Cerro del Almirez ultramafic massif (Sierra Nevada, Betic Cordillera, S. Spain) record the high-pressure dehydration of antigorite–olivine serpentinite to form chlorite harzburgite (ol + opx + chl). In the field, these two rock types are separated by a well-defined isograd. Titanian clinohumite (TiCl) and olivine show textural and compositional differences depending on the rock type. OH–TiCl occurs in the serpentinite as disseminated grains and in veins. F–OH–TiCl is observed exclusively in the chlorite harzburgite, where it occurs as porphyroblastic grains and within prograde olivine as irregular and lamellar, planar intergrowths at microscopic and submicroscopic scales. Petrological evidence of partial to complete breakdown of TiCl to olivine + ilmenite is preserved in both rock types. Chlorite harzburgite is characterized by a brown pleochroic olivine with abundantally oriented microscopic to submicroscopic oxide particles. The mean Ti-content of the brown olivine is 144 ppm. The brown olivine preserves TiCl lamellae that sometimes grade into ghost lamellae outlined by the oxide trails. This observation suggests that some of the oxide inclusions in the brown olivine are derived from the breakdown of TiCl intergrowths. Thermodynamic modelling of selected Almirez bulk rock compositions indicates a temperature increase from 635°C to 695°C, at pressures ranging from 1.7 GPa to 2.0 GPa, as the cause for the compositional adjustment of TiCl between the Almirez antigorite serpentinite and chlorite harzburgite. These P–T estimates are in good agreement with the sequence of phase relations observed in the field. The computed phase diagrams in conjunction with the geothermal conditions envisaged for different subduction settings indicate that TiCl is stable in the vicinity of the antigorite serpentinite/chlorite harzburgite phase boundary in some subduction settings. In these circumstances, clinohumite–olivine intergrowths in chlorite harzburgite may act as a sink for high field strength elements, and probably other elements, that are present in the mantle–wedge fluids.