Nature of magmatism and sedimentation at a Columbia active margin: Insights from combined U–Pb and Lu–Hf isotope data of detrital zircons from NW India

Detrital zircons from a Palaeoproterozoic quartzite, deposited between 1.85 and 1.82 Ga in the northern Aravalli orogen of NW India, show a distinctive age peak of ca. 1.85 Ga and variable, but largely subchondritic εHf_{1.85 Ga} between ? 1.3 and ? 21.0 corresponding to hafnium model ages of 2.5 to 3.6 Ga. These data indicate an important period of reworking of ancient (Eo- to Neoarchaean), strongly heterogeneous continental crust at this time. Prevalence of ca. 1.85 Ga subduction-related granitoids, almost identical U–Pb age spectra and εHf_t of detrital zircons in ca. 1.85 Ga metasedimentary rocks in the Aravalli orogen and the inner Lesser Himalaya indicate similar sediment provenances and thus a geological connection between these two terranes during late Palaeoproterozoic. All together, the data constrain a rapid succession of sedimentation, metamorphism and subduction-related magmatic activity and support the interpretation of an active geodynamic realm along the entire north Indian margin at ca. 1.85 Ga. Comparison of detrital zircon data in conjunction with published paleomagnetic data from north India and other crustal blocks of the Columbia supercontinent, additionally, suggest a close affinity of north India with Madagascar, the Cathaysia block of South China and South Korea during Columbia times.     

Multistage growth of Fe–Mg–carpholite and Fe–Mg–chloritoid,from field evidence to thermodynamic modelling

We provide new insights into the prograde evolution of HP/LT metasedimentary rocks on the basis of detailed petrologic examination, element-partitioning analysis, and thermodynamic modelling of well-preserved Fe–Mg–carpholite- and Fe–Mg–chloritoid-bearing rocks from the Afyon Zone (Anatolia). We document continuous and discontinuous compositional (ferromagnesian substitution) zoning of carpholite (overall X _Mg = 0.27–0.73) and chloritoid (overall X _Mg = 0.07–0.30), as well as clear equilibrium and disequilibrium (i.e., reaction-related) textures involving carpholite and chloritoid, which consistently account for the consistent enrichment in Mg of both minerals through time, and the progressive replacement of carpholite by chloritoid. Mg/Fe distribution coefficients calculated between carpholite and chloritoid vary widely within samples (2.2–20.0). Among this range, only values of 7–11 correlate with equilibrium textures, in agreement with data from the literature. Equilibrium phase diagrams for metapelitic compositions are calculated using a newly modified thermodynamic dataset, including most recent data for carpholite, chloritoid, chlorite, and white mica, as well as further refinements for Fe–carpholite, and both chloritoid end-members, as required to reproduce accurately petrologic observations (phase relations, experimental constraints, Mg/Fe partitioning). Modelling reveals that Mg/Fe partitioning between carpholite and chloritoid is greatly sensitive to temperature and calls for a future evaluation of possible use as a thermometer. In addition, calculations show significant effective bulk composition changes during prograde metamorphism due to the fractionation of chloritoid formed at the expense of carpholite. We retrieve P–T conditions for several carpholite and chloritoid growth stages (1) during prograde stages using unfractionated, bulk-rock XRF analyses, and (2) at peak conditions using compositions fractionated for chloritoid. The P–T paths reconstructed for the Kütahya and Afyon areas shed light on contrasting temperature conditions for these areas during prograde and peak stages.     

Geochemical and Sr–Nd isotopic characteristics of granitic rocks from northern Vietnam

Five major felsic igneous suites from northern Vietnam, with ages from mid-Proterozoic to early Cenozoic, were studied. Representative granitic rocks from the Posen Complex (mid-Proterozoic) and the Dienbien Complex (late Permian to early Triassic) show geochemical characteristics similar to those of calc-alkaline to high-K calc-alkaline I-type granites. However, the former, located in the South China block, has significantly higher initial Nd isotopic ratios [ε_Nd(T)=+0.7 to +1.5] and older Nd isotopic model ages (TDM∼1.7 Ga) than the latter [ε_Nd(T)=−4.7 to −9.7; T_DM∼1.3–1.5 Ga] which were emplaced south of the Song Ma Suture and thus in the Indochina block. The generation of both complexes may be attributed to subduction-related processes that occurred in two distinct crustal provenances with different degrees of mantle inputs. On the other hand, Jurassic to Cretaceous granitic rocks from the Phusaphin Complex, contemporaneous rhyolites from the Tule Basin, and late Paleogene granitic rocks from the Yeyensun Complex, all exposed in the South China block between the Ailao Shan–Red River shear zone and the Song Ma Suture, display geochemical features similar to those of A-type granites with intermediate ε_Nd(T) values (+0.6 to −2.8) and younger T_DM ages (0.6–1.1 Ga). These magmas are suggested to have been generated as a consequence of intraplate extension in the western part of the South China block (Yunnan), and to have been transported to their present position by mid-Tertiary continental extrusion along the Ailao Shan–Red River shear zone related to the India–Asia collision. Overall, the isotopic and model age data, reported in this study indicate that in northern Vietnam, the most important crust formation episode took place in the Proterozoic. Likewise, repeated mantle inputs have played a role in the petrogenesis of Phanerozoic granitic rocks.     

Native Alloys of the Pd–Pt and Ni–Cu–Al Systems from the AS Luna-24

The close intergrowth of two native alloys of the compositions Ni_0.59Cu_0.24Al_0.15Fe_0.01Mn_0.01 and Pd_0.55Pt_0.36Rh_0.09 with a size of 10 μm has been discovered in the regolith from the Mare Crisium. A conclusion on its exhalative origin is made.     

Genesis of Diamond in Metal–Carbon and Metal–Sulfur–Carbon Melts: Evidence from Experimental Data

Doklady Earth Sciences - The experimental data on diamond growth in the Fe–Ni–S–C and Fe–S–C systems with a sulfur content of 5–14 wt % at 5.5 GPa and...     

Coupled U–Pb–Hf of detrital zircons of Cambrian sandstones from Morocco and Sardinia: Implications for provenance and Precambrian crustal evolution of North Africa

U–Pb–Hf of detrital zircons from diverse Cambrian units in Morocco and Sardinia were investigated in order to clarify the sandstone provenance and how it evolved with time, to assess whether the detrital spectra mirror basement crustal composition and whether they are a reliable pointer on the ancestry of peri-Gondwanan terranes. Coupled with Hf isotopes, the detrital age spectra allow a unique perspective on crustal growth and recycling in North Africa, much of which is concealed below Phanerozoic sediments.In Morocco, the detrital signal of Lower Cambrian arkose records local crustal evolution dominated by Ediacaran (0.54–0.63 Ga) and Late-Paleoproterozoic (1.9–2.2 Ga; Eburnian) igneous activity. A preponderance of the Neoproterozoic detrital zircons possess positive ε_Hf(t) values and their respective Hf model ages (T_DM) concentrate at 1.15 Ga. In contrast, rather than by Ediacaran, the Neoproterozoic detrital signal from the Moroccan Middle Cambrian quartz-rich sandstone is dominated by Cryogenian-aged detrital zircons peaking at 0.65 Ga alongside a noteworthy early Tonian (0.95 Ga) peak; a few Stenian-age (1.0–1.1 Ga) detrital zircons are also distinguished. The majority of the Neoproterozoic zircons displays negative ε_Hf(t), indicating the provenance migrated onto distal Pan-African terranes dominated by crustal reworking. Terranes such as the Tuareg Shield were a likely provenance. The detrital signal of quartz–arenites from the Lower and Middle Cambrian of SW Sardinia resembles the Moroccan Middle Cambrian, but 1.0–1.1 Ga as well as ~ 2.5 Ga detrital zircons are more common. Therefore, Cambrian Sardinia may have been fed from different sources possibly located farther to the east along the north Gondwana margin. 1.0–1.1 Ga detrital zircons abundant in Sardinia generally display negative ε_Hf(t) values while 0.99–0.95 Ga detrital zircons (abundant in Morocco) possess positive ε_Hf(t), attesting for two petrologically-different Grenvillian sources. A paucity of detrital zircons younger than 0.6 Ga is a remarkable feature of the detrital spectra of the Moroccan and Sardinian quartz-rich sandstones. It indicates that late Cadomian orogens fringing the northern margin of North Africa were low-lying by the time the Cambrian platform was deposited. About a quarter of the Neoproterozoic-aged detrital zircons in the quartz-rich sandstones of Morocco (and a double proportion in Sardinia) display positive ε_Hf(t) values indicating considerable juvenile crust addition in North Africa, likely via island arc magmatism. A substantial fraction of the remaining Neoproterozoic zircons which possess negative ε_Hf(t) values bears evidence for mixing of old crust with juvenile magmas, implying crustal growth in an Andean-type setting was also significant in this region.     

U–Pb LA–ICP–MS Age of Detrital Zircons from the Lower Riphean and Upper Vendian Deposits of the Luga–Ladoga Monocline

The results of LA–ICP–MS U–Pb analyses of detrital zircons from the Precambrian deposits of Luga–Ladoga monocline are discussed. The age spectra of the zircons separated from the Riphean to Upper Vendian sandstones from the Shotkusa-1 well demonstrate dominance of the Paleo- and Mesoproterozoic grains while the Archaean zircons are subordinate. The Riphean debris sources were local swells of the Northern Ladoga basement. The sequence interval presumably corresponding to the Vasilieostrov Formation (Upper Vendian) has yielded not only Paleo- and Mesoproterozoic zircon ages, but Neoproterozoic as well, implying a Timanide provenance: these zircons (527 ± 9 and 516 ± 13 Ma) allow deposition of a significant part of the Shotkusa-1 sequence at the very beginning of the Cambrian.     

Timing of closure of the eastern Mongol–Okhotsk Ocean: Constraints from U–Pb and Hf isotopic data of detrital zircons from metasediments along the Dzhagdy Transect

The Mongol–Okhotsk Belt, a major structural element of East Asia, is probably the youngest orogenic segment within the Central Asian Orogenic Belt. However, the timing of final closure of the Mongol–Okhotsk Ocean remains unresolved. Here, we present detrital zircon U–Pb–Hf isotopic data and whole-rock geochemical data (major and trace elements and Sm-Nd isotopes) for the metasedimentary rocks from the Un'ya–Bom Terrane, Dzhagdy Terrane, and the eastern part of the Tukuringra Terrane. Our new zircon U-Pb ages suggest that all sedimentary formations along the Dzhagdy Transect are early Mesozoic in age, rather than Paleozoic as previously thought. The detrital zircons from the metasedimentary rocks in the Un'ya–Bom Terrane, the Dzhagdy Terrane, and the eastern part of the Tukuringra Terrane yielded the youngest concordant ages of 194 ± 4, 193 ± 2, and 171 ± 2 Ma, respectively. Moreover, we note that the so-called sedimentary formations of these terranes are not single sedimentary sequences as previously suggested, but a set of an olistostrome or tectonic mélanges composed of rocks of different ages and origins. These sedimentary formations are probably relics of the Mongol–Okhotsk remnant basin that formed in the “gaps” between the southern margin of the North Asian Craton and the Amur Block during their collision. The absence of detrital zircons younger than 171 Ma in the sedimentary rocks of the Mongol–Okhotsk basin implies that the final closure of this basin could have taken place at the boundary of the Early and Middle Jurassic as a result of the collision or the development of the Mongol–Okhotsk orogenic belt in this region. After that, the Mongol–Okhotsk Belt underwent intense deformation related to within-plate strike-slip faulting, which could be attributed to the late Mesozoic rotation of the North Asian Craton relative to the continental massifs of East Asia.     

Chemical composition of spinel from Uralian-Alaskan-type Mafic–Ultramafic complexes and its petrogenetic significance

Uralian-Alaskan-type mafic–ultramafic complexes are recognized as a distinct class of intrusions regarding lithologic assemblage, mineral chemistry and petrogenetic setting. In the present study, we discuss new data on the distribution of major elements in minerals of the spinel group in rocks from Uralian-Alaskan-type complexes in the Ural Mountains, Russia. Cr-rich spinel (Cr₂O₃ = 20–53 wt%) in dunite with interstitial clinopyroxene and in wehrlite cumulates indicate that it reacted with interstitial liquid resulting in the progressive substitution of Al₂O₂ and Cr₂O₃ by Fe₂O₃ and TiO₂. A distinct change in the spinel chemistry in dunite (Cr₂O₃ = 47–53 wt%), towards Al₂O₃- and Cr₂O₃-poor but Fe₂O₃-rich compositions monitors the onset of clinopyroxene fractionation in wehrlite (Cr₂O₃ = 15–35 wt%, Al₂O₃ = 1–8 wt%, Fe₂O₃ = 25–55 wt%). In more fractionated mafic rocks, the calculated initial composition of exsolved spinel traces the sustained crystallization of clinopyroxene by decreasing Cr₂O₃ and increasing FeO, Fe₂O₃ and fO₂. Finally, the initiation of feldspar crystallization buffers the Al₂O₃ content in most of the spinels in mafic rocks at very low Cr₂O₃ contents (<5 wt%). The fractionation path all along and the reaction with interstitial liquid are accompanied by increasing Fe₂O₃ contents in the spinel. This likely is caused by a significant increase in the oxygen fugacity, which suggests closed system fractionation processes. Spinel with Cr₂O₃ < 27 wt% is exsolved into a Fe₂O₃-rich and an Al₂O₃-rich phase forming a variety of textures. Remarkably, exsolved spinel in different lithologies from complexes 200 km apart follows one distinct solvus line defining a temperature of ca. 600°C. This indicates that the parental magmas were emplaced and eventually cooled at similar levels in the lithosphere, likely near the crust–mantle boundary. Eventually, these 600°C hot bodies were rapidly transported into colder regions of the upper crust during a regional tectonic event, probably during the major active phase of the Main Uralian Fault.     

Potential use of faujasite–phillipsite and phillipsite–chabazite tuff in purification of treated effluent from domestic wastewater treatment plants

Characterization of zeolitic tuff from Jabal Hannoun (HN) and Mukawir (MR) was carried out to examine the ability of using low-cost natural materials in domestic wastewater treatment. The grain size between 0.3 and 1 mm (0.3–1 mm) of the HN and MR has the highest total zeolite grade (faujasite–phillipsite and phillipsite–chabazite) and suitable cation exchange capacity. They were used as fixed-bed ion exchangers and adsorbents. The zeolitic tuff efficiently removed the organic and nitrogen compounds, Pb and Zn from the effluent. One bed volume (1 BV) of the zeolitic tuff is capable to remove up to 95 % of total organic carbon form 500 BV of the effluent. The removal percent of total nitrogen by HN and MR is close to 95 and 90 %, respectively. The zeolitic tuff has an excellent efficiency to remove Pb and Zn from the effluent. 1 BV of HN completely cleans Zn and Pb from 680 and 730 BV of the effluent, respectively, whereas 1 BV of MR is able to clean completely Zn and Pb from 500 and 685 BV of the effluent, respectively. The greater performance of the HN compared with the MR may be explained by its higher zeolites grade and presence of faujasite.     

Two pulses of mineralization and genesis of the Zhaxikang Sb–Pb–Zn–Ag deposit in southern Tibet: Constraints from Fe–Zn isotopes

Zhaxikang is one large Sb–Pb–Zn–Ag deposit located in the North Himalaya of southern Tibet. To date, the genesis of this deposit still remains controversial. Here, we present new pyrite Fe and sphalerite Zn isotopic data for the first three stages of mineralization, Fe–Zn isotopic data for Mn–Fe carbonate that formed during the first two stages of mineralization, and Zn isotopic data for the slate wall rocks of the Jurassic Ridang Formation to discuss the genesis of the Zhaxikang deposit. The overall δ⁵⁶Fe and δ⁶⁶Zn values range from −0.80‰ to 0.43‰ and from −0.03‰ to 0.38‰, respectively. The δ⁵⁶Fe values of Mn–Fe carbonates are lighter than those of associated pyrite in six mineral pairs, indicating that the iron carbonates are preferentially enriched in light Fe isotopes relative to pyrite. The sphalerite has lighter δ⁶⁶Zn values than associated Mn–Fe carbonates in three mineral pairs.The δ⁵⁶Fe values of pyrite that formed during the first three stages of mineralization gradually increase from stage 1 (−0.33‰ to −0.09‰) through stage 2 (−0.30‰ to 0.19‰) to stage 3 (0.16‰–0.43‰). In comparison, the sphalerite that formed during these stages has δ⁶⁶Zn values that gradually decrease from stage 1 (0.16‰–0.35‰) through stage 2 (0.09‰–0.23‰) to stage 3 (−0.03‰ to 0.22‰). These data, in conjunction with the observations of hand specimens and thin sections, suggest that the deposit was overprinted by a second pulse of mineralization. This overprint would account for these Fe–Zn isotopic variations as well as the kinetic Rayleigh fractionation that occurred during mineralization. The temporally increasing δ⁵⁶Fe and decreasing δ⁶⁶Zn values recorded in the deposit are also coincident with an increase in alteration, again supporting the existence of two pulses of mineralization. The δ⁵⁶Fe values of the first pulse of ore-forming fluid were calculated using theoretical equations, yielding values of −0.54‰ to −0.34‰ that overlap with those of submarine hydrothermal solutions (−1‰ to 0‰). However, the δ⁵⁶Fe values of the stage 3 pyrite are heavier than those of typical submarine hydrothermal solutions, which suggests that the second pulse of mineralization was probably derived from a magmatic hydrothermal fluid. In addition, the second pulse of ore-forming fluid has brought some Fe and taken away parts of Zn, which results the lighter δ⁶⁶Zn values of sphalerite and heavier δ⁵⁶Fe values of pyrite from the second pulse of mineralization. Overall, the Zhaxikang deposit records two pulses of mineralization, and the overprint by the second pulse of mineralization causes the lighter δ⁶⁶Zn values and heavier δ⁵⁶Fe values of modified samples.     

Ion microprobe U–Th–Pb geochronology and study of micro-inclusions in zircon from the Himalayan high- and ultrahigh-pressure eclogites,Kaghan Valley of Pakistan

We report ion microprobe U–Th–Pb geochronology of in situ zircon from the Himalayan high- and ultrahigh-pressure eclogites, Kaghan Valley of Pakistan. Combined with the textural features, mineral inclusions, cathodoluminescence image information and the U–Th–Pb isotope geochronology, two types of zircons were recognized in Group I and II eclogites. Zircons in Group I eclogites are of considerably large size (>100 μm up to 500 μm). A few grains are euhederal and prismatic, show oscillatory zoning with distinct core–rim luminescence pattern. Several other grains show irregular morphology, mitamictization, embayment and boundary truncations. They contain micro-inclusions such as muscovite, biotite, quartz and albite. Core or middle portions of zircons from Group I eclogites yielded concordant U–Th–Pb age of 267.6 ± 2.4 Ma (MSWD = 8.5), have higher U and Th contents with a Th/U ratio > 1, indicating typical magmatic core domains. Middle and rim or outer portions of these zircons contain inclusions of garnet, omphacite, phengite and these portions show no clear zonation. They yielded discordant values ranging between 210 and 71 Ma, indicating several thermal or Pb-loss events during their growth and recrystalization prior to or during the Himalayan eclogite-facies metamorphism. Zircons in Group II eclogites are smaller in size, prismatic to oval, display patchy or sector zoning and contain abundant inclusions of garnet, omphacite, phengite, quartz, rutile and carbonates. They yielded concordant U–Th–Pb age of 44.9 ± 1.2 Ma (MSWD = 4.9). The lower U and Th contents and a lower Th/U ratio (<0.05) in these zircons suggest their formation from the recrystallization of the older zircons during the Himalayan high and ultrahigh-pressure eclogite-facies metamorphism.     

Study of fossil wood from the Middle–Late Miocene sediments of Dhemaji and Lakhimpur districts of Assam,India and its palaeoecological and palaeophytogeographical implications

In order to reconstruct the palaeoclimate, a number of fossil wood pieces were collected and investigated from two new fossil localities situated in the Dhemaji and Lakhimpur districts of Assam. They belong to the Tipam Group considered to be of Middle–Late Miocene in age and show affinities with Gluta (Anacardiaceae), Bischofia (Euphorbiaceae), Bauhinia, Cynometra, Copaifera-Detarium-Sindora, Millettia-Pongamia, and Afzelia-Intsia (Fabaceae). The flora also records a new species of Bauhinia named Bauhinia miocenica sp. nov. The assemblage indicates a warm and humid climate in the region during the deposition of the sediments. The occurrence of some southeast Asian elements in the fossil flora indicates that an exchange of floral elements took place between India and southeast Asia during the Miocene.     

Metallogenesis and ore-forming time of the Changtuxili Mn–Ag–Pb–Zn deposit in Inner Mongolia: Evidence from C–O–S isotopes and U–Pb geochronology

This paper reports new geochronological (U–Pb) and isotope (C, O, and S) data to investigate the timing of mineralization and mode of ore genesis for the recently discovered Changtuxili Mn–Ag–Pb–Zn deposit, located on the western slopes of the southern Great Hinggan Range in NE China. The mineralization is hosted by intermediate–acidic lavas and pyroclastic rocks of the Baiyingaolao Formation. Three stages of mineralization are identified: quartz–pyrite (Stage I), galena–sphalerite–tetrahedrite–rhodochrosite (Stage II), and quartz–pyrite (Stage III). δ¹³C and δ¹⁸O values for carbonate from the ore vary from −8.51‰ to −4.96‰ and 3.97‰ to 15.90‰, respectively, which are indicative of a low-temperature alteration environment. δ³⁴S_V-CDT values of sulfides range from −1.77‰ to 4.16‰ and show a trend of equilibrium fractionation (δ³⁴S_Py ​> ​δ³⁴S_Sp ​> ​δ³⁴S_Gn). These features indicate that pyrite, sphalerite, and galena precipitated during the period of mineralization. The alteration mineral assemblage and isotope data indicate that the weakly acidic to weakly alkaline ore-forming fluid was derived largely from meteoric water and the ore-forming elements C and S originated from magma. During the mineralization, a geochemical barrier was formed by changes in the pH of the ore-forming fluid, leading to the precipitation of rhodochrosite. On the basis of the mineralization characteristics, new isotope data, and comparison with adjacent deposits, we propose that the Changtuxili Mn–Ag–Pb–Zn deposit is an intermediate-to low-sulfidation epithermal deposit whose formation was controlled by fractures and variability in the pH of the ore-forming fluid. The surrounding volcanic rocks yield zircon U–Pb ages of 160−146 ​Ma (Late Jurassic), indicating that the mineralization is younger than 146 ​Ma.     

Formation of the Japan Sea basin: Reassessment from Ar–Ar ages and Nd–Sr isotopic data of basement basalts of the Japan Sea and adjacent regions

Many studies have examined the Japan Sea basalts recovered during Ocean Drilling Program (ODP) Leg127/128. Of these, the ⁴⁰Ar–³⁹Ar dating undertaken is important in constraining the timing of the formation of the Japan Sea; however, the implications of their results do not appear to be fully appreciated by the geological community. In this paper, I reassess the ⁴⁰Ar–³⁹Ar age data of the basalts with reference to Nd–Sr isotopic data. The ⁴⁰Ar–³⁹Ar dating was performed on basalts somewhat enriched in large-ion lithophile elements and recovered from ODP Sites 794, 795 and the lower part of 797, yielding the plateau ages of 21.2–17.7 Ma. These basalts show the Nd–Sr isotopic signature of a moderately depleted mantle source (ε_Nd: 0.6–6.9). In contrast, the basalts from the upper part of Site 797 have yet to be dated due to their low K content, although their Nd isotopic compositions are similar to that of MORB (ε_Nd: 8.4–10.4). By analogy to the secular Nd–Sr isotopic trends reported for Sikhote-Alin and northeast Japan, the age of the upper basalts at Site 797 may be inferred to be younger than the lower basalts, probably around 16 Ma. The Nd–Sr isotopic compositions of the Japan Sea basalts have been interpreted in terms of eastward asthenospheric flow, as have the lavas of the Sikhote-Alin and northeastern Japan. The timing of volcanic activity in the Japan Sea region (i.e., from 21.2 to 14.86 Ma) is consistent with the timing of rotational crustal movements inferred from paleomagnetic studies of the Japanese Islands (i.e., 14.8–4.2 Ma for southwest Japan and 16.5–14.4 Ma for northeast Japan).     

Rates of zinc and trace metal release from dissolving sphalerite at pH 2.0–4.0

High-Fe and low-Fe sphalerite samples were reacted under controlled pH conditions to determine nonoxidative rates of release of Zn and trace metals from the solid-phase. The release (solubilization) of trace metals from dissolving sphalerite to the aqueous phase can be characterized by a kinetic distribution coefficient, (D_tr), which is defined as [(R_tr/X(tr)_Sph)/(R_Zn/X(Zn)_Sph)], where R is the trace metal or Zn release rate, and X is the mole fraction of the trace metal or Zn in sphalerite. This coefficient describes the relationship of the sphalerite dissolution rate to the trace metal mole fraction in the solid and its aqueous concentration. The distribution was used to determine some controls on metal release during the dissolution of sphalerite. Departures from the ideal D_tr of 1.0 suggest that some trace metals may be released via different pathways or that other processes (e.g., adsorption, solubility of trace minerals such as galena) affect the observed concentration of metals.     

Temporal–spatial distribution and tectonic setting of porphyry copper deposits in Iran: Constraints from zircon U–Pb and molybdenite Re–Os geochronology

Porphyry copper deposits (PCDs) in Iran are dominantly distributed in Arasbaran (NW Iran), the middle segment of the Urumieh–Dokhtar Magmatic Arc (UDMA), and Kerman (central SE Iran), with minor occurrences in eastern Iran and the Makran arc. This paper provides a temporal–spatial and geodynamic framework of the Iranian porphyry Cu (Mo–Au) systems, based on geochronologic data obtained from zircon U–Pb and molybdenite Re–Os dating of host porphyritic rocks and molybdenites in 15 major PCDs. The dating results define a long metallogenic duration (39–6 Ma), and suggest a long history of tectonic evolution from the accretionary orogeny related to early Cenozoic closure of the Neo-Tethys Ocean to subsequent collisional orogeny for the Iranian porphyry copper systems.The oldest porphyry mineralization occurred in the eastern part of Iran after the closure of a branch of the Neo-Tethyan (Sistan) Ocean between the Lut and Afghan blocks in the late Eocene (39–37 Ma). This was followed by mineralization in the Kerman porphyry copper belt over a time interval of about 20 m.y., where two metallogenic epochs have been recognized, including late Oligocene (29–27 Ma) and Miocene (18–6 Ma). The Bondar-e-Hanza deposit formed in the late Oligocene, while and the remaining dated deposits belong to Miocene epoch. According to the deposits' characteristics and their ages, the Miocene epoch can be divided into early, middle, and late stages. The Darreh Zar, Bakh Khoshk, Chah Firouzeh and Sar Kuh deposits formed during the early–middle Miocene. The largest porphyry deposits occur in the middle stage during the middle Miocene (14–11 Ma) and include the Sar Cheshmeh, Meiduk, Dar Alu and Now Chun deposits. These deposits were formed during crustal thickening, uplift, and rapid exhumation of the belt. The final stage of porphyry mineralization occurred during the late Miocene (9–6 Ma), and formed the Iju, Kerver, Kuh Panj and Abdar deposits.There were two porphyry mineralization stages in the Arasbaran porphyry copper belt in NW Iran, including an older late Oligocene (29–27 Ma) and a younger early Miocene (22–20 Ma) events. The Haft Cheshmeh deposit belongs to the older stage, and the world-class Sungun and Masjed Daghi deposits formed during the early Miocene.In the middle segment of the UDMA (Saveh–Yazd porphyry copper belt), PCDs formed during middle Miocene time (17–15 Ma). The geochronological results reveal that the porphyry mineralization moved from the northwest to southeast of UDMA over the time.Our dating results, combined with the possible late Eocene–Oligocene timing for collision between the Arabian and Iranian plates, support a model for Iranian PCD formation by partial melting of previously subduction-modified lithosphere in a post-subduction and post-collisional tectonic setting.     

Composition and conditions of crystallization of zircon from the rare-metal ores of the Gremyakha–Vyrmes Massif,Kola Peninsula

The first data on the composition and inner structure of zircon, one of the main ore minerals of the rare-metal metasomatites of the Gremyakha–Vyrmes alkaline-ultramafic massif, are reported. Early zircon generations are enriched in Y and REE and contain numerous inclusions of rock-forming and accessory minerals of metasomatites, as well as syngenetic fluid inclusions of calcite, thorite and thorianite. Late generations differ in the elevated Hf content and contain no inclusions. The elevated concentrations of Ca and Th in the central zones of crystals are related to the presence of numerous micron-sized inclusions of calcite and thorium phases. All zircon varieties have extremely low U and Pb contents. Concentrations and distribution patterns of incompatible and rare-earth elements in zircon from the metasomatites of the Gremyakha–Vyrmes Massif are similar to those of syenite pegmatites and magmatic carbonatites around the world. Mineral from these associations shows a positive Ce anomaly and elevated HREE contents. According to the compositions of zircon and thorite inclusion in it and experimental data on the simultaneous synthesis of these minerals, the crystallization temperature of zircon was 700–750°С. Using Ti-in-zircon temperature dependence, late zurcon was formed at temperature of 700–750°С. The rare-metal metasomatites are formed at the final stages of the massif formation, presumably after foidolites. Carbonatites could initiate metasomatic reworking of foidolites and accumulation of trace metals in them. The evolution of the primary alkaline–ultramafic melt toward the enrichment in trace elements was mainly controlled by crystallization differentiation.     

Elemental and organic geochemistry of Gondwana sediments from the Krishna–Godavari Basin,India

Elemental and organic geochemical studies have been carried out on the Gondwana sediments, collected from the outcrops of Permian and Jurassic–Cretaceous rocks in the Krishna–Godavari basin on the eastern coast of India, to understand their paleo and depositional environment and its implications for hydrocarbon generation in the basin. Amongst the studied formations, the Raghavapuram, Gollapalli and Tirupati form a dominant Cretaceous Petroleum System in the west of the basin. Raghavapuram shales and its stratigraphic equivalents are the source rock and Gollapalli and Tirupati sandstones form the reservoirs, along with basaltic Razole formation as the caprock. Major element systematics and X-ray diffraction study of the sandstones indicate them to be variably enriched with SiO₂ relative to Al₂O₃ and CaO, which is associated, inherently with the deposition and diagenesis of the Gondwana sediments. Post-Archean Average Shale normalized rare earth elements in shales show enrichment in most of the samples due to the increasing clay mineral and organic matter assemblage. A negative europium and cerium anomaly is exhibited by the REE's in majority of rocks. Composed primarily of quartz grains and silica cement, the Gollapalli and Tirupati sandstones have characteristics of high quality reservoirs. The shales show a significant increase in the concentration of redox sensitive trace elements, Ni, V, Cr, Ba and Zn. The total organic carbon content of the shales ranges between 0.1 and 0.5 wt%. Programmed pyrolysis of selected samples show the Tmax values to range between 352–497 °C and that of hydrogen index to be between 57–460 mgHC/gTOC. The organic matter is characterized by, mainly, gas prone Type III kerogen. The n-alkane composition is dominated by n-C₁₁–C₁₈ and acyclic isoprenoid, phytane. The aromatic fraction shows the presence of naphthalene, anthracene, phenanthrene, chrysene and their derivatives, resulting largely from the diagenetic alteration of precursor terpenoids. The organic geochemical proxies indicate the input of organic matter from near-shore terrestrial sources and its deposition in strongly reducing, low oxygen conditions. The organic matter richness and maturity derived from a favorable depositional setting has its bearing upon the Gondwana sediments globally, and also provides promising exploration opportunities, particularly in the Raghavapuram sequence of the KG basin.