Geochemistry of amphibolitized eclogites and cross-cutting tonalitic–trondhjemitic dykes in the Metamorphic Kimi Complex in East Rhodope (N.E. Greece): implications for partial melting at the base of a thickened crust

In the ultra-high pressure Metamorphic Kimi Complex widespread tonalitic–trondhjemitic dykes, with an intrusion age ca. 65–63 Ma, cross-cut boudins and layers of amphibolitized eclogites. Geochemical investigation proclaims the tied genetic relationship of the amphibolitized eclogites and the associated tonalitic–trondhjemitic dykes. The major and trace element contents and rare earth element patterns of the amphibolitized eclogites indicate formation of their protoliths by fractional crystallization of tholeiitic magmas in a back-arc environment. The tonalites and trondhjemites are characterized by moderate to high Sr contents (>130 ppm), and low Y (<8.2 ppm) and heavy rare earth element contents (Yb content of 0.19–0.88 ppm). The chemical composition of the tonalitic and trondhjemitic dykes are best explained by partial melting of a tholeiitic source like the amphibolitized eclogites with residual garnet and amphibole, at the base of a thickened crust during Early Tertiary subduction/accretion at the southern margins of the European continent.     

New P–T constraints on the Tamayen glaucophane‐bearing rocks,eastern Taiwan: Perple_X modelling results and geodynamic implications

New pseudosection modelling was applied to better constrain the P–T conditions and evolution of glaucophane‐bearing rocks in the Tamayen block of the Yuli belt, recognized as the world's youngest known blueschist complex. Based on the predominant clinoamphibole, textural relationships, and mineral compositions, these glaucophane‐bearing high‐P rocks can be divided into four types. We focused on the three containing garnet. The chief phase assemblages are (in decreasing mode): amphibole + quartz + epidote + garnet + chlorite + rutile/titanite (Type‐I), phengite + amphibole + quartz + garnet + chlorite + epidote + titanite + biotite + magnetite (Type‐II), and amphibole + quartz + albite + epidote + garnet + rutile + hematite + titanite (Type‐III). Amphibole exhibits compositional zoning from core to rim as follows: glaucophane → pargasitic amphibole → actinolite (Type‐I), barroisite → Mg‐katophorite/taramite → Fe‐glaucophane (Type‐II), glaucophane → winchite (Type‐III). Using petrographic data, mineral compositions and Perple_X modelling (pseudosections and superimposed isopleths), peak P–T conditions were determined as 13 ± 1 kbar and 550 ± 40 °C for Type‐I, 10.5 ± 0.5 kbar and 560 ± 30 °C for Type‐II (thermal peak) and 11 ± 1 kbar and 530 ± 30 °C for Type‐III. The calculations yield higher pressures and temperatures than previously thought; the difference is ~1–6 kbar and 50–200 °C. The three rock types record similar P–T retrograde paths with clockwise trajectories; all rocks followed trajectories with substantial pressure decrease under near‐isothermal conditions (Type‐I and Type‐III), with the probable exception of Type‐II where decompression followed colder geotherms. The P–T paths suggest a tectonic environment in which the rocks were exhumed from maximum depths of ~45 km within a subduction channel along a relative cold geothermal gradient of ~11–14 °C km^?1.     

Dolomitic marbles from the ultrahigh-pressure metamorphic Kimi complex in Rhodope, N.E. Greece

Summary Dolomitic marbles from the Organi and Pandrosos areas of the ultrahigh-pressure (UHP) metamorphic Kimi complex in East Rhodope, N.E. Greece have the mineral assemblage: Cal + Dol + Ol + Phl ± Di ± Hbl ± Spl ± Ti–Chu + retrograde Srp and Chl. Several generations of calcite and dolomite with variable composition and texture represent different stages of the P–T evolution: The first stage is represented by matrix dolomite ( = 0.48) and relic domains of homogenous composition in matrix calcite ( = 0.11–0.13); the second stage is evident from precipitation of lath-shaped and vermicular dolomite in matrix calcite. The third stage is represented by veinlets of almost pure CaCO₃ and domainal replacement of prior calcite by nearly pure CaCO₃ + Ca-rich dolomite ( = 0.34–0.43). Matrix dolomite adjacent to CaCO₃ veinlets also becomes Ca-rich ( = 0.42). In fact, Ca-rich dolomites with in the range of 0.40–0.34 are reported for the first time from metamorphic marbles. Coexisting Ca-rich dolomite and Mg-poor calcite cannot be explained by the calcite-dolomite miscibility gap. This assemblage rather suggests that Mg-poor calcite was aragonite originally, which formed together with Ca-rich dolomite according to the reaction Mg–Cal → Arg + Dol (1) at ultrahigh pressures and temperatures above at least 850 °C, when dolomite becomes disordered and incorporates more Ca than coexisting aragonite does in terms of Mg. The simplest explanation of these observations probably is to suggest two metamorphic events: The first one represented by relic matrix carbonates at relatively low to moderate pressures and temperatures of ca. 750 °C, and the second one limited by the minimum temperatures for dolomite disorder (ca. 850 °C) and in the aragonite + dolomite stability field, i.e. at a minimum pressure of 3 GPa and, if the presence of diamond-bearing metapelites nearby is considered, at conditions of at least 850 °C and 4.3 GPa in the diamond stability field. As there is hardly any back-reaction of Ca-rich dolomite + Mg-poor calcite to Mg-rich calcite, peak temperatures remained below the reaction (1) and the exhumation path probably crossed the aragonite-calcite transition at much lower than peak temperature. Cooling and decompression must have both occurred extremely fast in order for the μm-sized Ca-rich dolomite textures to be preserved. An alternative explanation of the formation of “UHP”-textures and compositions is by a fluid influx that not only caused serpentinisation and chloritisation of silicates but also Mg-leaching from carbonates, particularly from Mg-rich calcite and its fine grained dolomite-precipitates, thus transforming them into Mg-poor calcite + Ca-rich dolomite.     

Petrogenesis of Ultramafic Rocks from the Ultrahigh-pressure Metamorphic Kimi Complex in Eastern Rhodope (NE Greece)

Widespread bodies of garnet–spinel metaperidotites withpyroxenitic layers occur in the ultrahigh-pressure metamorphicKimi Complex. In this study we address the origin of such peridotite–pyroxeniteassociations in the context of polybaric melting regimes. Weconduct a detailed geochemical investigation of major and traceelement relations and compare them with a range of major elementmodelling scenarios. With increasing bulk-rock MgO content,the garnet–spinel metaperidotites exhibit decreasing CaO,Al₂O₃, TiO₂, and Na₂O along with increasing Ni and a graduallyincreasing Zr/Zr* anomaly, consistent with an origin as residuesafter variable degrees of melt extraction. The major elementmodelling further suggests a polybaric adiabatic decompressionmelting regime beginning at high to ultrahigh pressure, withan intermediate character between pure batch and fractionalmelting and a mean extent of melting of 9–11%. The pyroxenitesexhibit major element compositions that cannot be reproducedby experimental or calculated melts of peridotite. Moreover,the Kimi pyroxenites have highly variable Ni and Sc contentsand a wide range of Mg-number (0· 76–0·89), inconsistent with an origin as frozen melts or the productsof melt–peridotite interaction. However, both the majorelement systematics and the observed rare earth element patterns,with both convex and concave shapes, can be explained by anorigin as clinopyroxene-rich, high-pressure cumulates involvinggarnet and/or Cr-spinel. KEY WORDS: peridotite; pyroxenite; partial melting; UHP metamorphism; cumulate     

Tracing high-pressure metamorphism in marbles: Phase relations in high-grade aluminous calcite–dolomite marbles from the Greek Rhodope massif in the system CaO–MgO–Al2O3–SiO2–CO2 and indications of prior aragonite

Four different types of parageneses of the minerals calcite, dolomite, diopside, forsterite, spinel, amphibole (pargasite), (Ti–)clinohumite and phlogopite were observed in calcite–dolomite marbles collected in the Kimi-Complex of the Rhodope Metamorphic Province (RMP). The presence of former aragonite can be inferred from carbonate inclusions, which, in combination with an analysis of phase relations in the simplified system CaO–MgO–Al₂O₃–SiO₂–CO₂ (CMAS–CO₂) show that the mineral assemblages preserved in these marbles most likely equilibrated at the aragonite–calcite transition, slightly below the coesite stability field, at ca. 720 °C, 25 kbar and a_CO2 ~ 0.01. The thermodynamic model predicts that no matter what activity of CO₂, garnet has to be present in aluminous calcite–dolomite-marble at UHP conditions.     

Continental rift and oceanic protoliths of mafic–ultramafic rocks from the Kechros Complex,NE Rhodope (Greece): implications from petrography,major and trace-element systematics,and MELTS modeling

The whole-rock chemistry of eclogites, partially amphibolitized eclogites, and dyke amphibolites from the metamorphic Kechros complex in the eastern Rhodope Mountains preserves evidence of the geodynamic framework for the origin of their protoliths. Major and trace-element concentrations define two distinct protolith groups for the eclogites. The low-Fe–Ti (LFT) eclogites have low-TiO₂ content (<0.67 wt%), negative high field strength element anomalies, and variable enrichments in large ion lithophile elements (LILE). The rare earth element (REE) patterns are characterized by strong light-REE (LREE) enrichment and heavy-REE (HREE) depletion. The high-Fe–Ti (HFT) eclogites have small to moderate LILE enrichment and lack Nb anomalies. The REE patterns of the HFT eclogites are characterized by LREE depletion and relatively flat MREE–HREE patterns. The rock compositions and petrographic features of the LFT eclogites resemble gabbros formed in a continental rift environment with minor to moderate contamination of a mantle-derived mafic magma by continental crust, whereas the HFT eclogites resemble mafic rocks formed in extensional oceanic environments. We interpret the HFT suite to represent a later stage in an evolution from continental rift to open ocean, following the origin of the LFT suite. Dyke amphibolite compositions, except for probable SiO₂ loss associated with metamorphic dehydration reactions, appear to represent liquid compositions quenched in conduits through the lower crust. MELTS modeling shows that dyke amphibolite compositions can be related to each other by fractional crystallization under strongly oxidizing conditions at ~0.5 GPa pressure, and all can be derived from a low-degree melt of modified fertile peridotite from around 1.7 GPa. Cumulates crystallized from the parental liquids of the amphibolites under oxidizing conditions may have yielded the protoliths of the HFT suite.     

Strewn field,mineralogy, and petrology of Al Haggounia 001: A unique enstatite chondrite

In this work, we investigate macroscopic characteristics, magnetic susceptibility, mineralogy, and mineral composition of Al Haggounia 001. The samples were collected during eight field missions in the period between 2015 and 2019. In the strewn field of about 65 km in length, the specimens are found either on the surface or shallowly buried in loose sediments, which rules out the previous suggestions that this meteorite is a fossil meteorite. Macroscopically, the samples exhibit three major lithologies with various colors, porosities, and distributions of oxidized veins. The data obtained using transmitted and reflected light microscopy, scanning electron microscopy, and electron microprobe analysis confirm the macroscopic observations and show a heterogenous distribution of silicates and metal sulfides. Al Haggounia 001 is composed of enstatite, plagioclase, kamacite, taenite, schreibersite, daubreelite, troilite, graphite, sinoite, and silica polymorphs. We identified a new type of chondrules that are flattened and composed of rods of albite and enstatite, as well as elongated nodules of metal and sulfides, in addition to compression fractures in the form of subparallel veinlets. These features presumably reflect the deformation caused by shock. The magnetic susceptibility of Al Haggounia 001 (4.39 ± 0.20) is much lower than that of usual EH (5.48 ± 0.16) and EL (5.46 ± 0.04) chondrites but is in the range of E finds (5.05 ± 0.43). The thermomagnetic and hysteresis measurements are controlled by type, size, distribution of metal-sulfide nodules, arrangement of oxyhydroxide veins, and weathering. Al Haggounia 001 is an anomalous meteorite with a polymict nature. It records multiple events revealing its unique origin which expends the groups of enstatite chondrites and provides insights into the complex formation and evolution history of their parent body.     

Petrography and geochemistry of the enriched basaltic shergottite Northwest Africa 2975

We present a study of the petrology and geochemistry of basaltic shergottite Northwest Africa 2975 (NWA 2975). NWA 2975 is a medium‐grained basalt with subophitic to granular texture. Electron microprobe (EMP) analyses show two distinct pyroxene compositional trends and patchy compositional zoning patterns distinct from those observed in other meteorites such as Shergotty or QUE 94201. As no bulk sample was available to us for whole rock measurements, we characterized the fusion crust and its variability by secondary ion mass spectrometer (SIMS) measurements and laser ablation inductively coupled plasma spectroscopy (LA‐ICP‐MS) analyses as a best‐available proxy for the bulk rock composition. The fusion crust major element composition is comparable to the bulk composition of other enriched basaltic shergottites, placing NWA 2975 within that sample group. The CI‐normalized REE (rare earth element) patterns are flat and also parallel to those of other enriched basaltic shergottites. Merrillite is the major REE carrier and has a flat REE pattern with slight depletion of Eu, parallel to REE patterns of merrillites from other basaltic shergottites. The oxidation state of NWA 2975 calculated from Fe‐Ti oxide pairs is NNO‐1.86, close to the QFM buffer. NWA 2975 represents a sample from the oxidized and enriched shergottite group, and our measurements and constraints on its origin are consistent with the hypothesis of two distinct Martian mantle reservoirs: a reduced, LREE‐depleted reservoir and an oxidized, LREE‐enriched reservoir. Stishovite, possibly seifertite, and dense SiO₂ glass were also identified in the meteorite, allowing us to infer that NWA 2975 experienced a realistic shock pressure of ~30 GPa.     

Geochemistry of the Serifos calc-alkaline granodiorite pluton,Greece: constraining the crust and mantle contributions to I-type granitoids

International Journal of Earth Sciences - The Late Miocene (11.6–9.5&nbsp;Ma) granitoid intrusion on the island of Serifos (Western Cyclades, Aegean Sea) is composed of syn- to...     

Mineral chemistry of the Tissint meteorite: Indications of two‐stage crystallization in a closed system

The Tissint meteorite is a geochemically depleted, olivine‐phyric shergottite. Olivine megacrysts contain 300–600 μm cores with uniform Mg# (~80 ± 1) followed by concentric zones of Fe‐enrichment toward the rims. We applied a number of tests to distinguish the relationship of these megacrysts to the host rock. Major and trace element compositions of the Mg‐rich core in olivine are in equilibrium with the bulk rock, within uncertainty, and rare earth element abundances of melt inclusions in Mg‐rich olivines reported in the literature are similar to those of the bulk rock. Moreover, the P Kα intensity maps of two large olivine grains show no resorption between the uniform core and the rim. Taken together, these lines of evidence suggest the olivine megacrysts are phenocrysts. Among depleted olivine‐phyric shergottites, Tissint is the first one that acts mostly as a closed system with olivine megacrysts being the phenocrysts. The texture and mineral chemistry of Tissint indicate a crystallization sequence of: olivine (Mg# 80 ± 1) → olivine (Mg# 76) + chromite → olivine (Mg# 74) + Ti‐chromite → olivine (Mg# 74–63) + pyroxene (Mg# 76–65) + Cr‐ulvöspinel → olivine (Mg# 63–35) + pyroxene (Mg# 65–60) + plagioclase, followed by late‐stage ilmenite and phosphate. The crystallization of the Tissint meteorite likely occurred in two stages: uniform olivine cores likely crystallized under equilibrium conditions; and a fractional crystallization sequence that formed the rest of the rock. The two‐stage crystallization without crystal settling is simulated using MELTS and the Tissint bulk composition, and can broadly reproduce the crystallization sequence and mineral chemistry measured in the Tissint samples. The transition between equilibrium and fractional crystallization is associated with a dramatic increase in cooling rate and might have been driven by an acceleration in the ascent rate or by encounter with a steep thermal gradient in the Martian crust.