Mantle–crust interactions during Variscan subduction in the Eastern Alps (Nonsberg–Ulten zone): geochronology and new petrological constraints

We have analyzed the Sm–Nd and Rb–Sr whole-rock and mineral isotope systematics of garnet peridotites and associated eclogites and migmatitic gneisses from the Nonsberg–Ulten zone of the Eastern Alps. The garnet peridotites include coarse-grained varieties, characterized by well-preserved to slightly modified mantle geochemical signatures, and finer-grained varieties enriched in amphibole and LILE. Hydration of some of the most strongly deformed, fine-grained peridotites by crustal fluids caused isotopic disequilibrium between the peridotite minerals, preventing accurate age determinations. The coarse-grained peridotites, the eclogites and the country migmatitic gneisses yield garnet–whole-rock and garnet–clinopyroxene Sm–Nd ages that indicate for all rock types an isotopic homogenization event at ca. 330 Ma. The similar ages suggest that all rock types shared a common history since the incorporation of the peridotites in the crust, and constrain the garnet-facies metamorphism of the peridotites, as well as partial melting of the crust, to an episode of crustal subduction at the end of the Variscan orogenic cycle.     

Strontium isotope geochemistry of alpine tectonite lherzolites: Data compatible with a mantle origin

Constituent minerals from three alpine lherzolites (Beni Bouchera, Morocco; Lanzo, Italy; and Ronda, Spain) and a clinopyroxene from the Othris complex, Greece, reveal the following range in Sr isotopic composition: clinopyroxenes, 0.70228–0.70370; orthopyroxenes, 0.70265–0.70429; and olivines, 0.70290–0.70831. Collectively the data: (1) indicate that whole-rock lherzolites (weighted recalculations of ⁸⁷Sr/⁸⁶Sr= 0.7025–0.7028) have isotopic compositions which attest to a simple mantle origin and not the complex models proposed to date; (2) are incompatible with the published range for alpine peridotites 0.7063–0.7290; (3) reveal either similar or different isotopic compositions for coexisting minerals, the latter possibly being the result of Rb mobility and introduction of radiogenic Sr into the peridotite system; and (4) indicate the past existence of liquids with “alkalic” affinities within the lherzolite framework. The lherzolites are therefore believed to be residual, having experienced a small degree of partial melting.     

Petrology of the Yugu peridotites in the Gyeonggi Massif,South Korea: Implications for its origin and hydration process

Peridotites exposed in the Yugu area in the Gyeonggi Massif, South Korea, near the boundary with the Okcheon Belt, exhibit mylonitic to strongly porphyroclastic textures, and are mostly spinel lherzolites. Subordinate dunites, harzburgites, and websterites are associated with the lherzolites. Amphiboles, often zoned from hornblende in the core to tremolite in the rim, are found only as neoblasts. Porphyroclasts have recorded equilibrium temperatures of about 1000°C, whereas neoblasts denote lower temperatures, about 800°C. Olivines are Fo_90–91 in lherzolites and Fo₉₁ in a dunite and a harzburgite. The Cr# (= Cr/(Cr + Al) atomic ratio) of spinels varies together with the Fo of olivines, being from 0.1 to 0.3 in lherzolites and around 0.5 in the dunite and harzburgite. The Na₂O content of clinopyroxene porphyroclasts is relatively low, around 0.3 to 0.5 wt% in the most fertile lherzolite. The Yugu peridotites are similar in porphyroclast mineral chemistry not to continental spinel peridotites but to sub‐arc or abyssal peridotites. Textural and mineralogical characteristics indicate the successive cooling with hydration from the upper mantle to crustal conditions for the Yugu peridotites. Almost all clinopyroxenes and amphiboles show the same U‐shaped rare earth element (REE) patterns although the level is up to ten times higher for the latter. The hydration was associated with enrichment in light REE, resulting from either a slab‐derived fluid or a fluid circulating in the crust. The mantle‐wedge or abyssal peridotites were emplaced into the continental crust as the Yugu peridotite body during collision of continents to form a high‐pressure metamorphic belt in the Gyeonggi Massif. The peridotites from the Gyeonggi Massif exhibit lower‐pressure equilibration than peridotites, with or without garnets, from the Dabie–Sulu Collision Belt, China, which is possibly a westward extension of the Gyeonggi Massif.     

Mineralogic variability of the uppermost mantle along mid-ocean ridges

Modal analyses of 273 different peridotites representing 43 dredge stations in the Atlantic, Caribbean, and Indian Oceans define three separate melting trends. Peridotites dredged in the vicinity of “mantle plumes” or hot spots have the most depleted compositions in terms of basaltic components, while peridotites dredged at locations removed from such regions are systematically less depleted. The modal data correlate well with mineral compositions, with the peridotites most depleted in pyroxene also having the most refractory mineral compositions. This demonstrates that they are the probable residues of variable degrees of mantle melting. Further, there is a good correlation between the modal compositions of the peridotites and the major element composition of spatially associated dredged basalts. This demonstrates for the first time that the two must be directly related, as is frequently postulated. The high degree of depletion of the peridotites in basaltic major element components in the vicinity of some documented mantle plumes provides direct evidence for a thermal anomaly in such regions—justifying their frequent designation as “hot spots”. The high incompatible element concentrations in these “plume” basalts, however, are contrary to what is expected for such high degrees of melting, and thus require either selective contributions from locally more abundant enriched veins and/or contamination by a volatile-rich metasomatic front from depth.     

Mixed mantle provenance: diverse garnet compositions in polymict peridotites, Kaapvaal craton, South Africa

Garnet compositions are used to understand mantle petrogenesis and to reconstruct the lithostratigraphy of the shallow mantle (<200 km). However, garnets in polymict peridotites from the Kaapvaal craton (>2500 Ma) have a centimeter-scale elemental and stable isotopic variability suggestive of a mixed mantle provenance. The chemical heterogeneity of the garnets is similar to that reported from rocks sampled over a considerable depth and temperature range within the lower lithosphere. For example garnets found in polymict peridotites are similar to garnets found in sheared and granular peridotites, ‘cold’ and ‘hot’ lherzolites, peridotitic (P-type) diamond inclusions, and garnets from polybaric (50-200 km) peridotites (i.e. spinel, garnet and diamond facies). These data indicate that the Kaapvaal cratonic root has been disturbed by complex processes possibly associated with crack propagation and entrainment that juxtaposed garnet-bearing lithologies of diverse petrogenesis, provenance and depth. This has preserved chemical disequilibrium in the high pressure minerals in what is, in effect, a mantle breccia possibly associated with kimberlite precursors.     

Garnet clinopyroxenite xenolith from Dish Hill,California

A single garnet clinopyroxenite xenolith found at the Dish Hill basanite cone near Ludlow, California, has well developed unmixing and reaction textures like those found in garnet pyroxenite inclusions in Hawaiian, African and Australian basalts and like those of pyroxenites in some European alpine peridotites. Reconstructed pyroxene compositions suggest that before unmixing the rock consisted of clinopyroxene and about 10% garnet plus spinel, but all of the garnet may have been dissolved in clinopyroxene. Most or all of the garnet formed by exsolution from clinopyroxene and by reaction between clinopyroxene and spinel in an open system. Following exsolution, the rock was deformed and partly recrystallized in the solid state. Similarity of compositions of exsolved and recrystallized minerals suggests recrystallization at P-T conditions similar to those of exsolution.The rock is not the chemical equivalent of the host basanite and cannot represent magma of basanitic composition crystallized in the mantle. Its history of deformation and recrystallization, like that of accompanying spinel lherzolite inclusions, supports the idea that the garnet clinopyroxenite is an accidental inclusion derived from the upper mantle.     

Effects of melt percolation on the Re-Os systematics of continental mantle lithosphere: A case study of spinel peridotite xenoliths from Heilongjiang,NE China

Os isotope ratios of mantle peridotites have been considered to be largely immune to recent melt-rock interaction. However, Os isotope ratios and PGE (Platinum group elements) concentrations of the Yong’an xenoliths have been significantly modified by melt percolation, and are not suitable for determining the formation age of lithosphere mantle in Yong’an. In this study, the Yong’an spinel peridotite xenoliths are divided into two groups: N-Type and E-Type. The N-Type group including cpx (clinopyroxene)-poor lherzolite and harzburgite, shows a large variation of Cr#(sp) (13.2-48) and sulfur contents (from 171 ppm to below detection limit), whereas the E-Type peridotites are mainly refractory harzburgites and are characterized by high Cr#(sp) (35.3-42.2) and overall low sulfur contents (below 51 ppm). Both types show similar major and REE (rare earth element) patterns. Furthermore, the N-Type peridotites display a restricted range of iridium-group PGE (IPGE), Os/Ir and Ru/Ir ratios (Os/Ir = 0.64-1.12, Ru/Ir = 1.52-1.79) and variable palladium-group PGE (PPGE) contents (3.4-14.9 ppb), whereas the E-Type peridotites show a large variation of Os/Ir and Ru/Ir ratios (Os/Ir = 0.33-0.84, Ru/Ir = 0.94-1.6), and a restricted range of PPGE (4.3-6.9 ppb). 187Os/188Os ratios of E-Type peridotites are higher than those of N-Type peridotites at comparable fertility levels. These results suggest that N-Type peridotites may have been overprinted by metasomatism via small melt fractions, in which the percolation of the volatile-rich, small melt fractions only resulted in LILE (large ion lithophile element) enrichment of clinopyroxene, and their whole rock PGE contents and Re-Os isotope values were little changed. Moreover, E-Type peridotites may have been modified by melt-rock reaction involving relatively large melt fractions, which may result in the formation of secondary cpx and olivine and the removal of IPGE-bearing minerals such as Ru-Os-(Ir) alloys or laurite, followed by precipitation of secondary sulfides from melt with radiogenic isotopic signature.     

Thrusting of young lithosphere in subduction zones with special reference to structures in ophiolitic peridotites

Two contrasted types of structures have been recognized in peridotites from ophiolites and from the oceanic environment. The first one, typical of high-temperature/moderate-stress conditions, is observed in the upper part of ophiolitic peridotites and has been ascribed to plastic flow in an oceanic ridge environment. The second one, typical of moderate-temperature/high-stress conditions, is more specially dealt with here. It is printed in the peridotites above the basal metamorphic aureole found in many ophiolites. The strain increases downward over 1–2 km to produce peridotite mylonites at the contact with the metamorphic aureole. Similarities with rocks from trench and island arc environments suggest ascribing this deformation in ophiolites to a trench environment. We propose that shear fracturing in a young oceanic lithosphere is initiated by the compressive elastic stress in its lower part which is produced by bending of the subducted plate. An externally applied compressive stress is responsible for subsequent overthrusting of the fractured lithosphere. This interpretation is in good agreement with the available geophysical data on young subducted plates and with the physical data on ophiolitic peridotites.     

碳酸盐化橄榄岩的电性研究

为进一步探讨上地幔的高导层成因,了解碳酸盐在上地幔电性方面的作用并估算上地幔高导层的碳酸盐含量,本文对不同碳酸盐含量的橄榄岩及玄武岩样品在2~3 GPa、300~1300℃的条件下进行了电性实验研究.研究初步发现:碳酸盐熔体显著增强橄榄岩、玄武岩样品的导电能力;单纯用含硅酸盐熔体的橄榄岩或单纯用含水橄榄岩可能难以解释上地幔某些区域的异常高导现象;同样,单纯用碳酸盐化的橄榄岩可能也难以解释上地幔某些区域的高导现象;上地幔的高导区很可能是碳酸盐熔体、硅酸盐熔体及水的共存区域.     

Deep melting and sodic metasomatism underneath the highly oblique-spreading Lena Trough (Arctic Ocean)

Abyssal peridotites collected along the highly oblique-spreading Lena Trough north of Greenland and Spitsbergen have mineral compositions that are similar to residual abyssal peridotites, except for high sodium concentrations in clinopyroxene (cpx). Most samples are lherzolites with light rare earth element (REE)-depleted cpx trace element patterns, but significantly fractionated middle to heavy REE ratios at relatively high heavy REE concentrations. Such characteristics can only be explained by initial melting of a garnet peridotite followed by low degrees of melting in the stability field of spinel peridotite. The residual garnet signature requires either a high potential temperature of the upwelling mantle, or elevated solidus-lowering water contents. The limited spinel field melting suggests a deep cessation of melt extraction, possibly because of the presence of a thick lithospheric cap. This is consistent with the extremely low effective spreading rate and the vicinity to a passive continental margin, which allow conductive cooling to reach deeper levels than commonly estimated for faster mid-ocean ridges. High sodium concentrations in cpx are neither explainable by melt refertilization, nor by a simple diffusion mechanism. The efficient fractionation of sodium from the light REE requires post-melting metasomatism, which is typically restricted to the subcontinental lithosphere. This might imply that the Lena Trough peridotites represent unroofed subcontinental mantle, from which no melt was extracted during the opening of the Lena Trough. It is more likely that sodic metasomatism occurred after partial melting underneath the Lena Trough, and that such an enrichment process is responsible for elevated sodium concentrations in abyssal peridotites elsewhere. Sodium in cpx of residual peridotites can therefore not serve as an indicator of partial melting or melt refertilization.     

Na and Cr contents in clinopyroxenes from peridotites: A possible discriminant between “sub-continental” and “sub-oceanic” mantle

The compilation of data available in the literature and new analyses show that clinopyroxenes are significantly richer in Na and poorer in Cr in peridotites associated with high-grade metamorphic rocks than in ultramafites from oceanic environments, considered as “sub-continental” or “sub-oceanic” mantle, respectively. Two distinctive fields can be drawn in the Na-Cr plot. This fact is related to the large amount of basic magma provided by the oceanic mantle along the mid-oceanic ridges.Application of this Na-Cr diagram to clinopyroxenes from peridotites in orogenic belts and appearing as xenoliths in volcanic rocks and kimberlites (“nodules”) allows us to specify their origin, taking into consideration that the clinopyroxene composition is controlled by several factors each of which gives rise to a particular trend:P-T. conditions, mineral facies, partial melting and crystal fractionation, metasomatism. It appears that oceanic-type mantle may be found under continents in extensional areas having evolved towards rift systems, and in ophiolites. The latter exhibit different degree of depletion related to their formation in two main geotectonic situations: mid-oceanic ridges and active margin systems.     

地幔矿物中硫化物熔体包裹体的成因

中国东部新生代碱性玄武岩中产出的巨晶、辉石岩和橄榄岩等地幔捕虏体内硫化物熔体包裹体的矿物组成不尽相同,反映了它们成因上的差异巨晶中除有磁黄铁矿相的硫化物熔体包裹体外还有一些磁黄铁矿士黄铜矿上镍黄铁矿共生的硫化物熔体包裹体这反映它们是在成分接近于上地幔硫化物平均组成的硫化物液滴逐步冷却过程中形成,即首先在1000℃以上的高温晶出单硫化物固溶体（MSS）,然后在大约850℃晶出黄铜矿（固溶体）,最后在610-300℃下由MSS中溶离出镍黄铁矿辉石岩中硫化物熔体包裹体有磁黄铁矿和镍黄铁矿,而橄榄岩中主要为镍黄铁矿这表明地慢部分熔融造成残余的橄榄岩中硫化物包裹体富Ni,生成镍黄铁矿;而在部分熔融期间作为堆晶产出的辉石岩变得相对贫Ni,可以生成磁黄铁矿．另外,Ni在橄榄石和辉石矿物中分配系数的不同也许是另一个原因河北汉诺坝、福建明溪和闽清的二辉橄榄岩中出现的硫化物都是镍黄铁矿,也表明它们经历过地幔部分熔融.     

Petrology of the Green Knobs diatreme and implications for the upper mantle below the Colorado Plateau

Peridotite inclusions, crystal fragments, and kimberlite breccia at Green Knobs, New Mexico, have been studied to evaluate compositions and processes in the upper mantle below the Colorado Plateau. Most peridotite inclusions are spinel lherzolites and harzburgites, or their partly hydrated equivalents, in the Cr-diopside group. Orthopyroxene-rich websterites and olivine websterites comprise 3% of the peridotites and formed as cumulates. Typical anhydrous or slightly hydrated peridotites contain aluminous, calcic diopside (5–7% Al₂O₃), aluminous orthopyroxene (3–6% Al₂O₃), spinel, and olivine (near Fa₉). Geothermometers based on different mineral pairs yield temperatures from above 1100°C to below 700°C in single rocks. High values, derived from pyroxenes with included exsolution lamellae, may approximate temperatures of primary crystallization. Low values, based on olivine-spinel and olivine-clinopyroxene pairs, approach upper mantle temperatures before eruption. In rare samples, some spinel grains are rimmed by garnet while others are not rimmed; garnet formation was controlled by nucleation kinetics. About one-third of the peridotites were deformed shortly before eruption, with effects ranging from mild cataclasis to the production of ultramylonites.Discrete crystals of garnet, olivine (near Fa₈), and Cr-diopside represent garnet peridotite. Eclogites were not found. The garnet peridotite is more depleted than overlying spinel peridotite, and it is not a likely source for the minettes associated with the kimberlites.The mantle below Green Knobs consists of spinel peridotite from 45 to perhaps 60 km depth immediately underlain by more-depleted garnet peridotite. The position of the spinel-garnet transition may be fixed by kinetics. The kimberlite may have been produced when heat from ascending minette magma released volatiles from otherwise depleted garnet peridotite. Resulting gas-solid mixtures erupted along zones of deformation associated with Colorado Plateau monoclines. Sheared lherzolites formed during renewed movement along these zones.     

Subduction-zone peridotites and their records of crust-mantle interaction

Subduction is the core process of plate tectonics. The mantle wedge in subduction-zone systems represents a key tectonic unit, playing a significant role in material cycling and energy exchange between Earth's layers. This study summarizes research progresses in terms of subduction-related peridotite massifs, including supra-subduction zone(SSZ) ophiolites and mantle-wedge-type(MWT) orogenic peridotites. We also provide the relevant key scientific questions that need be solved in the future. The mantle sections of SSZ ophiolites and MWT orogenic peridotites represent the mantle fragments from oceanic and continental lithosphere in subduction zones, respectively. They are essential targets to study the crust-mantle interaction in subduction zones. The nature of this interaction is the complex chemical exchanges between the subducting slab and the mantle wedge under the major control of physical processes. The SSZ ophiolites can record melt/fluid-rock interaction, metamorphism,deformation, concentration of metallogenic elements and material exchange between crust and mantle, during the stages from the generation of oceanic lithosphere at spreading centers to the initiation, development, maturation and ending of oceanic subduction at continental margins. The MWT orogenic peridotites reveal the history of strong metamorphism and deformation during subduction, the multiple melt/fluid metasomatism(including silicatic melts, carbonatitic melts and silicate-bearing C-HO fluids/supercritical fluids), and the complex cycling of crust-mantle materials, during the subduction/collision and exhumation of continental plates. In order to further reveal the crust-mantle interaction using subduction-zone peridotites, it is necessary to utilize high-spatial-resolution and high-precision techniques to constrain the complex chemical metasomatism, metamorphism,deformation at micro scales, and to reveal their connections with spatial-temporal evolution in macro-scale tectonics.     

Metasomatic hydrous fluids in amphibole peridotites from Zabargad Island (Red Sea)

Combining textural, petrological, chemical and isotopic (Sr, H and O) data for amphiboles and whole rocks from the Zabargad peridotite diapir allows three different events to be distinguished. During each event, which can be related to a specific tectonic process of the rifting of the Red Sea, hydrous fluids produced amphiboles.

The first and the second generations of amphiboles have characteristics consistent with the involvement of mantle-derived hydrous fluids. The first generation consists of scarce Ti-pargasites which crystallized from small amounts of fluid at temperatures of around 900–1000°C. Their growth was linked to magma percolation in the peridotites before their deformation during diapiric uplift. The second generation consists of Cr-pargasites which crystallized locally (and abundantly) during reaction between the peridotites and a sodium/potassium-bearing hydrous fluid at temperatures of around 700–800°C. These amphiboles grew synchronously with the diapiric uplift. The hydrous fluids probably originated in the sub-continental mantle and were released during the diapiric uplift of the peridotites.

The third generation consists of amphiboles (pargasitic hornblende, hornblende sensu lato and tremolite) which are localized in shear zones and veins. They crystallized at temperatures estimated between 700°C and 450°C, again from a sodium/potassium-bearing hydrous fluid. However, this fluid is extraneous to the peridotites, as shown by the Sr, H and O isotope compositions which suggest seawater penetration either during or after the final emplacement of the peridotite diapir.

Although the peridotite diapir was emplaced in granulitic gneisses of the pan-African deep continental crust, no evidence was found for a contribution of hydrous continental fluids in the production of the amphiboles present in the peridotite bodies of Zabargad Island.     

Relation between mantle shear zone deformation and metasomatism in spinel peridotite xenoliths of Jeju Island (South Korea): Evidence from olivine CPO and trace elements

This study presents geochemical and fabric analysis of coarse-grained, porphyroclastic and mylonitic spinel peridotite xenoliths derived from the shallow subcontinental lithospheric mantle of Jeju Island (South Korea). Fabric analysis of olivines in the studied peridotites shows activation of the high temperature (0 1 0)[1 0 0] slip system; however, in the porphyroclastic and mylonitic peridotites, activation of (0 k l)[1 0 0] slip system results in a weaker fabric. Formation of porphyroclastic and mylonitic fabrics are thought to form in a shear-dominated environment. The results of the trace element analysis reveal that the smaller the grain size and weaker the fabric, the more enriched in LREE and HFSE are the peridotites, which indicates a strong relationship between metasomatic agents and mantle shear zones.     

Geochemical constraints on the origin and tectonic setting of the serpentinized peridotites from the Paleoproterozoic Nyong series,Eseka area,SW Cameroon

Serpentinized rocks closely associated with Paleoproterozoic eclogitic metabasites were recently discovered at Eseka area in the northwestern edge of the Congo craton in southern Cameroon.Here,we present new field data,petrography,and first comprehensible wholerock geochemistry data and discuss the protolith and tectonic significance of these serpentinites in the region.The studied rock samples are characterized by pseudomorphic textures,including mesh microstructure formed by serpentine intergrowths with cores of olivine,bastites after pyroxene.Antigorite constitutes almost the whole bulk of the rocks and is associated(to the less amount) with tremolite,talc,spinel,and magnetite.Whole-rock chemistry of the Eseka serpentinites led to the distinction of two types.Type 1 has high MgO( 40 wt%) content and high Mg#values(88.80) whereas Type 2 serpentinite samples display relatively low MgO concentration and Mg#values(40 and 82.88 wt%,respectively).Both types have low Al/Si and high Mg/Si ratios than the primitive mantle,reflecting a refractory abyssal mantle peridotite protolith.Partial melting modeling indicates that these rocks were derived from melting of spinel peridotite before serpentinization.Bulk rock high-Ti content is similar to the values of subducted serpentinites( 50 ppm).This similarity,associated with the high Cr contents,spinel-peridotite protolith compositions and Mg/Si and Al/Si ratios imply that the studied serpentinites were formed in a subductionrelated environment.The U-shaped chondrite normalizedREE patterns of serpentinized peridotites,coupled with similar enrichments in LREE and HFSE,suggest the refertilized nature due to melt/rock interaction prior to serpentinization.Based on the results,we suggest that the Eseka serpentinized peridotites are mantle residues that suffered a high degree of partial melting in a subductionrelated environment,especially in Supra Subduction Zone setting.These new findings suggest that the Nyong series in Cameroon represents an uncontested Paleoproterozoic suture zone between the Congo craton and the Sao Francisco craton in Brazil.     

Characteristics of subcontinental lithospheric mantle beneath Baegryeong Island, Korea: Spinel peridotite xenoliths

Abstract   Geochemical data on Baegryeong Island spinel peridotites found in Miocene alkali basalt provide the information for lithosphere composition, chemical processes, equilibrium pressure and temperature conditions. Spinel peridotite xenoliths, showing transitional textures between protogranular and porpyroclastic textures, were accidentally trapped by the ascending alkali basalt magma. The xenoliths originate at depths from 50 to 70 km with a temperature range from 800 to 1100°C. The variations of modal and mineral compositions of the spinel peridotite xenoliths indicate that the xenoliths have undergone 1–10% fractional melting. The spinel peridotites from Baegryeong Island have undergone cryptic mantle metasomatism subsequent to melt extraction. Metasomatic agent of enriched spinel peridotite xenoliths was carbonatite melt.     

After the peak water: the increasing influence of rock glaciers on alpine river systems

Human‐accelerated climate change is quickly leading to glacier‐free mountains, with consequences for the ecology and hydrology of alpine river systems. Water origin (i.e., glacier, snowmelt, precipitation, and groundwater) is a key control on multiple facets of alpine stream ecosystems, because it drives the physico‐chemical template of the habitat in which ecological communities reside and interact and ecosystem processes occur. Accordingly, distinct alpine stream types and associated communities have been identified. However, unlike streams fed by glaciers (i.e., kryal), groundwater (i.e., krenal), and snowmelt/precipitation (i.e., rhithral), those fed by rock glaciers are still poorly documented. We characterized the physical and chemical features of these streams and investigated the influence of rock glaciers on the habitat template of alpine river networks. We analysed two subcatchments in a deglaciating area of the Central European Alps, where rock glacier‐fed, groundwater‐fed, and glacier‐fed streams are all present. We monitored the spatial, seasonal, and diel variability of physical conditions (i.e., water temperature, turbidity, channel stability, and discharge) and chemical variables (electrical conductivity, major ions, and trace element concentrations) during the snowmelt, glacier ablation, and flow recession periods of two consecutive years. We observed distinct physical and chemical conditions and seasonal responses for the different stream types. Rock glacial streams were characterized by very low and constant water temperatures, stable channels, clear waters, and high concentrations of ions and trace elements that increased as summer progressed. Furthermore, one rock glacier strongly influenced the habitat template of downstream waters due to high solute export, especially in late summer under increased permafrost thaw. Given their unique set of environmental conditions, we suggest that streams fed by thawing rock glaciers are distinct river habitats that differ from those normally classified for alpine streams. Rock glaciers may become increasingly important in shaping the hydroecology of alpine river systems under continued deglaciation.     

Mineral chemical composition and geodynamic significance of peridotites from Nain ophiolite,central Iran

The peridotites from north of the town of Nain in central Iran consist of clinopyroxene-bearing harzburgite and lherzolite with small lenses of dunite and chromitite pods. The lherzolite contains aluminous spinel with a Cr number (Cr^# = Cr/[Cr + Al]) of 0.17. The Cr number of spinels in harzburgite and chromitite is 0.38–0.42 and 0.62, respectively. This shows that the lherzolite and harzburgite resulted from <18% of partial melting of the source materials. The estimated temperature is 1100 ± 200 °C for peridotites, the estimated pressure is <15 ± 2.3 kbar for harzburgites and >16 ± 2.3 kbar for lherzolites and estimated fo₂ is 10^?1±0.5 for peridotites. Discriminant geochemical diagrams based on mineral chemistry of harzburgites indicate a supra-subduction zone (SSZ) to mid-oceanic ridge (MOR) setting for these rocks. On the basis of their Cr^#, the harzburgite and lherzolite spinels are analogous to those from abyssal peridotites and oceanic ophiolites, whereas the chromites in the chromitite (on the basis of Cr^# and boninitic nature of parental melts) resemble those from SSZ ophiolitic sequences. Therefore, the Nain ophiolite complex most likely originated in an oceanic crust related to supra-subduction zone, i.e. back arc basin. Field observations and mineral chemistry of the Nain peridotites, indicating the suture between the central Iran micro-continent (CIM) block and the Sanandaj–Sirjan zone, show that these peridotites mark the site of the Nain–Baft seaway, which opened with a slow rate of ocean-floor spreading behind the Mesozoic arc of the Sanandaj–Sirjan zone as a result of change of Neo Tethyan subduction régime during middle Cretaceous.