Alteration and mineralization at the Zhibula Cu skarn deposit,Gangdese belt,Tibet

The Zhibula Cu skarn deposit contains 0.32 Mt. Cu metal with an average grade of 1.64% and is located in the Gangdese porphyry copper belt in southern Tibet. The deposit is a typical metasomatic skarn that is related to the interaction of magmatic–hydrothermal fluids and calcareous host rock. Stratiform skarn orebodies occur at the contact between tuff and marble in the Lower Jurassic Yeba Formation. Alteration zones generally grade from a fresh tuff to a garnet-bearing tuff, a garnet pyroxene skarn, and finally to a wollastonite marble. Minor endoskarn alteration zonations are also observed in the causative intrusion, which grade from a fresh granodiorite to a weakly chlorite-altered granodiorite, a green diopside-bearing granodiorite, and to a dark red-brown garnet-bearing granodiorite. Prograde minerals, which were identified by electron probe microanalysis include andradite–grossularite of various colors (e.g., red, green, and yellow) and green diopside. Retrograde metamorphic minerals overprint the prograde skarn, and are mainly composed of epidote, quartz, and chlorite. The ore minerals consist of chalcopyrite and bornite, followed by magnetite, molybdenite, pyrite, pyrrhotite, galena, and sphalerite. Three types of fluid inclusions are recognized in the Zhibula deposit, including liquid-rich two-phase inclusions (type L), vapor-rich two-phase inclusions (type V), and daughter mineral-bearing three-phase inclusions (type S). As the skarn formation evolved from prograde (stage I) to early retrograde (stage II) and later retrograde (stage III), the ore-forming fluids correspondingly evolved from high temperature (405–667 °C), high salinity (up to 44.0 wt.% NaCl equiv.), and high pressure (500–600 bar) to low-moderate temperature (194–420 °C), moderate-high salinity (10.1–18.3 and 30.0–44.2 wt.% NaCl equiv.), and low-moderate pressure (250–350 bar). Isotopic data of δ³⁴S (− 0.1‰ to − 6.8‰, estimated δ³⁴S_fluids = − 0.7‰), δD_H2O (− 91‰ to − 159‰), and δ¹⁸O_H2O (1.5‰ to 9.2‰) suggest that the ore-forming fluid and material came from magmatic–hydrothermal fluids that were associated with Miocene Zhibula intrusions. Fluid immiscibility likely occurred at the stage I and stage II during the formation of the skarn and mineralization. Fluid boiling occurred during the stage III, which is the most important Cu deposition mechanism for the Zhibula deposit.     

Geochemical signatures of Late Holocene paleo-hydrological changes from Phulera and Pokharan saline playas near the eastern and western margins of the Thar Desert,India

Stratigraphical, mineralogical, geochemical and optical dating methods were used to reconstruct paleo-hydrological changes in two playas (Phulera, 500 mm/a and Pokharan, 200 mm/a) in near extremum climatic regions of the Thar Desert. Sediment successions in shallow profiles from Phulera and Pokharan contain three and four stratigraphic units, respectively, each with characteristic geochemical properties. These units reflect changes in chemical weathering, detrital input, salinity and provide a measure of the changes in precipitation (i.e. monsoon) through time.Sediments from Pokharan suggest short rainfall events during ca. 6.6–4 ka, relatively stable fresh water (higher and persistent rainfall) regime during 4–2.3 ka, and a hyper saline (low rainfall) condition during 2.3–1.1 ka. Sediments at Phulera, record hyper saline (low rainfall) lacustrine conditions during <2.3 ka to >1.4 ka. Higher abundance of gypsum in Pokharan (2.3–1.1 ka) and proto-dolomite in Phulera (2.3–1.4 ka) are nearly synchronous and reflect enhancement of salinity. Selenite crystals in Pokharan and large desiccation cracks in buried horizons at Phulera reflect desiccation of playas at ca. 2 ka. Both playas progressively became less saline after 1.4 ka. Given the regional nature of this record, these changes are attributed to fluctuation of the monsoon over the Indian sub continent.     

Holocene glacier history of Bjørnbreen and climatic reconstruction in central Jotunheimen,Norway, based on proximal glaciofluvial stream-bank mires

Holocene variations of Bjørnbreen, Smørstabbtinden massif, west-central Jotunheimen are reconstructed from the lithostratigraphy of two alpine stream-bank mires flooded episodically by meltwater. The approach uses multiple sedimentological indicators (weight loss-on-ignition, mean grain size, grain-size fractions, bulk density, moisture content and magnetic susceptibility), an a priori model of overbank deposition of suspended glaciofluvial sediments, a detailed chronology based on 56 radiocarbon dates, and a Little Ice Age sedimentological analogue. Rapid, late-Preboreal deglaciation was indicated by immigration of Betula pubescens by 9700 cal. BP. An interval of at least 3000 years in the early Holocene when glaciers were absent was interrupted by two abrupt episodes of glacier expansion around the time of the Finse Event, the first at ca 8270–7900 cal. BP (Bjørnbreen I Event) and the second at ca 7770–7540 cal. BP (Bjørnbreen II Event). Neoglaciation began shortly before ca 5730 cal. BP with gradual build-up to the maximum of the Bjørnbreen III Event at ca 4420 cal. BP. Later maxima occurred at ca 2750 cal. BP (Bjørnbreen IV Event) and at 1300, 1260, 1060 and 790 cal. BP (all within the Bjørnbreen V Event). Glaciers were smaller than today and possibly melted away on several occasions in the late Holocene (ca 3950, 1410 and 750 cal. BP). Minor maxima also occurred at ca 660 and 540 cal. BP, within the late Mediaeval Warm Period and the early Little Ice Age, respectively. The Little Ice Age maximum was dated to 213±25 BP (ca 205 cal. BP). The relative magnitudes of the main glacier maxima were determined: Erdalen Event>Little Ice Age Event (Bjørnbreen VI)>Bjørnbreen I (Finse Event) ≈ Bjørnbreen II>Bjørnbreen V⩾Bjørnbreen IV>Bjørnbreen III. These episodic events of varying magnitude and abruptness were used in conjunction with an independent summer-temperature proxy to reconstruct variations in equilibrium-line altitude (ELA) and a Holocene record of winter precipitation. Since the Preboreal, ELA varied within a range of about 390 m, and winter precipitation ranged between 40 and 160% of modern values. Winter precipitation variations appear to have been the main cause of these century- to millennial-scale Holocene glacier variations.     

Estuarine–fluvial floodplain formation in the Holocene Lower Tagus valley (Central Portugal) and implications for Quaternary fluvial system evolution

We present a brief synthesis of the Quaternary fluvial record in the Lower Tagus Basin (central Portugal), concentrating on factors controlling infill and incision. The Holocene part of the record forms the focus of this paper and guides the questioning of the basic assumptions of the established Quaternary fluvial evolution model, in particular the link between sea-level change and fluvial incision-deposition. We suggest that several incision-aggradation phases may have occurred during glacial periods. Major aggradation events may overlap with cold episodes, while incision appears to concentrate on the warming limb of climate transitions. The complex stratigraphy of the Quaternary record in the Lower Tagus valley is influenced by repeated base-level and climate changes.This paper submits the first chronostratigraphic framework for valley fill deposits in the Lower Tagus area. Sea-level rise forced aggradation and controlled deposition of the fine-grained sedimentary wedge underlying the low-gradient Lower Tagus floodplain. Investigations have focused on the lower Muge tributary, where rapidly aggrading estuarine and fluvial environments were abruptly established (∼8150 cal BP) as sea level rose. Base level at the valley mouth controlled the upstream extent of the fine-grained backfill. Tidal environments disappeared abruptly (∼5800 cal BP) when the open estuary at the Muge confluence was infilled by the Tagus River. The decrease and final still stand of sea-level rise led to floodplain stabilisation with peat (∼6400–5200 cal BP) and soil formation (∼5200–2200 cal BP). Localised renewed sedimentation (∼2200–200 cal BP) is linked to human activity.     

The processes and mechanisms of severe sandstorm development in the eastern Hexi Corridor China,during the Last Glacial period

Dust transported by sandstorms has been an important feedback in climate change in the past, and its environmental effects are predicted to have a great impact on future global climatic change. Investigating the grain-size classes and the standard deviations of the modern sandstorm samples, and the samples in the Shagou section (situated in the eastern Hexi Corridor), lead us to suggest that the sand fraction within the range of 275.4–550 μm in this section can be used as a sensitive indicator of severe sandstorms. We selected the size range in the L1 stratum of the Shagou loess section as indicative of temporal changes in sandstorm intensity in the eastern Hexi Corridor and found that during the Last Glacial period, severe sandstorms in the eastern Hexi Corridor occurred with high frequency during these periods: I (70–54 ka B.P.), II (51–48 ka B.P.), III (45–42 ka B.P.), IV (38–33 ka B.P.), V (31–28 ka B.P.) and VI (26–12 ka B.P.) In general, the frequency and intensity of dust storms in the early (MIS 4) and late (MIS 2) periods were both high but they were reduced in the middle period (MIS 3). The primary factors controlling severe sandstorms are hydrology and wind power, followed by the expansion of the source extent. Reduced precipitation caused the source region of sandstorms to expand; in addition, wind speeds also increased at this time. These factors may have directly contributed to the abundance of severe sandstorms. Based on the grain size from a loess section (the Shagou section) in the eastern Hexi Corridor, we propose an evolutionary sequence of the severe sandstorms during the Last Glacial period. This sequence is consistent with the dust records in the Arctic, the Antarctic and low-latitude (the central equatorial Pacific) areas. Thus globally synchronous periods of high dust activity occurred in the Last Glacial period. The strong winds proposed here provide a potential explanation for the global consistency of dust flux changes during the Last Glacial period.     

Relict sand wedges in southern Patagonia and their stratigraphic and paleo-environmental significance

Relict sand wedges are ubiquitous in southern Patagonia. At six sites we conducted detailed investigations of stratigraphy, soils, and wedge frequency and characteristics. Some sections contain four or more buried horizons with casts. The cryogenic features are dominantly relict sand wedges with an average depth, maximum apparent width, minimum apparent width, and H/W of 78, 39, 3.8, and 2.9 cm, respectively. The host materials are fine-textured (silt loam, silty clay loam, clay loam) till and the infillings are aeolian sand. The soils are primarily Calciargidic Argixerolls that bear a legacy of climate change. Whereas the sand wedges formed during very cold (?4 to ?8 °C or colder) and dry (ca. ≤100 mm precipitation/yr) glacial periods, petrocalcic horizons from calcium carbonate contributed by dustfall formed during warmer (7 °C or warmer) and moister (≥250 mm/yr) interglacial periods. The paleo-argillic (Bt) horizons reflect unusually moist interglacial events where the mean annual precipitation may have been 400 mm/yr. Permafrost was nearly continuous in southern Patagonia during the Illinoian glacial stage (ca. 200 ka), the early to mid-Pleistocene (ca. 800–500 ka), and on two occasions during the early Pleistocene (ca. 1.0–1.1 Ma).     

Anatomy of garnets in a Jurassic granite from the south-eastern margin of the North China Craton: Magma sources and tectonic implications

The Late Jurassic Jingshan granite located at the south-eastern margin of the North China Craton contains abundant garnets which can be subdivided into three types based on texture and composition: (i) euhedral garnet in mafic biotite and garnet rich enclave (Grt I), (ii) coarse-grained garnet (Grt II) in the host granite, and (iii) small euhedral garnet in aplite (Grt III). In general, Grt I has higher FeO, CaO and lower MnO contents than Grt II. Grt III has higher Mn, but lower Ca contents than others. Grt I has lower MREE and HREE contents than Grt II. Grt III has prominent and distinctly negative Eu anomaly as well as higher MREE composition compared to the others. Systematic variations in oxygen isotope compositions are observed among the three garnet types, with δ¹⁸O values of <3.8‰ in most of Grt I, 3.8–4.7‰ in most Grt II (for inclusion-free garnets), and typically >4.7‰ in Grt III. Some of the Grt II and Grt III display two distinct zonings with cores having similar major and trace element compositions to Grt I.Cathodoluminescence (CL) images revealed that the zircons from different garnet-bearing samples possess fine-scale oscillatory zoned magmatic rims with inherited cores. In situ zircon U–Pb dating and trace element analyses show that the dark-luminescent magmatic rims all have Jurassic concordia ages (∼160 Ma) and similar trace element patterns. Most of the inherited cores also display similar Triassic ages of 210–236 Ma, which is similar to the ages of ultrahigh pressure (UHP) metamorphic rocks of the Dabie–Sulu orogen (230 Ma). In addition, Jurassic concordia ages were also found in a zircon inclusion in Grt I, implying that the Grt I was formed shortly before the main magmatic event. The age data suggest that the three different garnet types may be genetically related and modified by cogenetic magmatic events.Based on the zircon U–Pb ages from different garnet-bearing samples, the major element, trace element, oxygen isotope, and zoning textures of the three kinds of garnet we suggest that Grt I may be peritectic garnet, whereas Grt II and III are probably the results of magmatic dissolution–precipitation processes and re-equilibration of garnets with changing magmatic conditions during melting, differentiation, crystallization, and cooling within the granite. We conclude from the oxygen isotopic character of the garnets and ages of the zircons that the source rocks for the Jingshan granites are from Dabie–Sulu orogen representing the South China Craton.     

Kinetics of chromate reduction by pyrite and biotite under acidic conditions

The removal of chromate from aqueous solutions, using finely ground pyrite and biotite, was investigated by batch experiments. The kinetics and mechanism of chromate reduction are discussed here. Chromate reduction by pyrite was about 100 times faster than that by biotite, and was also faster at pH 3 than 4. When pyrite was used, more than 90% of the initial chromate was reduced within 4 h at pH 4, and within 40 min. at pH 3. However, with biotite more than 400 h was required for the reduction of 90% of the initial chromate. The results indicate that the rate of chromate reduction was strongly depending on the amount and dissolution rate of the Fe(II) in the minerals. The reduction of chromate at pH 4 resulted in the precipitation of (Cr, Fe)(OH)_3(s), which is believed to have limited the concentrations of dissolved Cr(III) and Fe(III) to less than the expected values. When biotite was used, the amounts of decreased Fe(II) and reduced Cr(VI) showed no stoichiometric relationship, which implies that not only was there chromate reduction by Fe(II) ions in the acidic solution, but also heterogeneous reduction of Fe(III) ions by structural Fe(II) in biotite. However, the results from a series of the experiments using pyrite showed that the concentrations of the decreased Fe(II) and the reduced Cr(VI) were close to the stoichiometric ratio of 3:1. This was because the oxidation of pyrite rapidly created Fe(II) ions, even in oxygenated solutions, and the chromate reduction by the Fe(II) ions was significantly faster than the Fe(II) ion oxygenation. When compared with the experimental sets controlled at an initial pH of 3, the pH of the biotite batch, which was not controlled, increased to 3.4. Because of the increase in the pH, Cr(VI) was not completely removed, and 25% (1.2–1.3 mg/L Cr(VI)) of the initial concentration remained for up to 1000 h. The pH increase is, in most cases, caused by the hydrolysis of clay minerals. However, in the pyrite batches, there was no difference in the variations of the chromate reduction in relation to the pH control. There was also no difference in the capacity and rate of Cr(VI) reduction in 0.01 M NaCl or Na₂SO₄ solutions. In the 0.01 M NaH₂PO₄ solution pyrite experiment, the Cr(VI) was not completely removed, despite the maintenance of the pH at 3. The dominant Fe species was about 10 mg/L Fe(III) and few Fe(II) ions existed in solution. The Fe phosphate (Fe₃(PO₄)₂ or FePO₄) coatings on the surface of pyrite prevented access of O₂ or Cr(VI). Therefore, the surface coatings are likely to have caused the deterioration of the Cr(VI) reduction capacity in the NaH₂PO₄ solution.     

In–situ LA–ICP–MS trace elemental analyzes of magnetite: The Tieshan skarn Fe–Cu deposit,Eastern China

The Tieshan Fe–Cu deposit is located in the Edong district, which represents the westernmost and largest region within the Middle–Lower Yangtze River Metallogenic Belt (YRMB), Eastern China. Skarn Fe–Cu mineralization is spatially associated with the Tieshan pluton, which intruded carbonates of the Lower Triassic Daye Formation. Ore bodies are predominantly located along the contact between the diorite or quartz diorite and marbles/dolomitic marbles. This study investigates the mineral chemistry of magnetite in different skarn ore bodies. The contrasting composition of magnetite obtained are used to suggest different mechanisms of formation for magnetite in the western and eastern part of the Tieshan Fe–Cu deposit. A total of 178 grains of magnetite from four magnetite ore samples are analyzed by LA–ICP–MS, indicating a wide range of trace element contents, such as V (13.61–542.36 ppm), Cr (0.003–383.96 ppm), Co (11.12–187.55 ppm) and Ni (0.19–147.41 ppm), etc. The Ti/V ratio of magnetite from the Xiangbishan (western part of the Tieshan deposit) and Jianshan ore body (eastern part of the Tieshan deposit) ranges from 1.32 to 5.24, and 1.31 to 10.34, respectively, indicating a relatively reduced depositional environment in the Xiangbishan ore body. Incorporation of Ti and Al in magnetite are temperature dependent, which hence propose that the temperature of hydrothermal fluid from the Jianshan ore body (Al = 3747–9648 ppm, with 6381 ppm as an average; Ti = 381.7–952.0 ppm, with 628.2 ppm as an average) was higher than the Xiangbishan ore body (Al = 2011–11122 ppm, with 5997 ppm as an average, Ti = 302.5–734.8, with 530.8 ppm as an average), indicating a down–temperature precipitation trend from the Jianshan ore body to the Xiangbishan ore body. In addition, in the Ca + Al + Mn versus Ti + V diagram, magnetite is plotted in the skarn field, consideration with the ternary diagram of TiO₂–Al₂O₃–MgO, proposing that the magnetite ores are formed by replacement, instead of directly crystallized from iron oxide melts, which provide a better understanding regarding the composition of ore fluids and processes responsible for Fe mineralization in the Tieshan Fe–Cu deposit.     

The post-collisional Cihai iron skarn deposit,eastern Tianshan,Xinjiang, China

The Cihai iron skarn deposit is located in the southern part of the eastern Tianshan, Xinjiang, northwestern China. The major iron orebodies are banded and nearly parallel to each other. The iron ores are hosted in an early diabase dike and in skarn. Post-ore diabase dikes cut the iron ores and their hosting diabase. Hydrothermal activity can be divided into four stages based on geological and petrographic observations: initial K–Na alteration (stage I), skarn-minor magnetite event (II), retrograde skarn-magnetite main ore event (III), and quartz–calcite–sulfide veining (IV). Zircon U–Pb dating yields ages of 286.5 ± 1.8 Ma for early diabase and 275.8 ± 2.2 Ma for post-ore diabase dikes. Amphibole separated from massive magnetite ore gives a ⁴⁰Ar–³⁹Ar plateau age of 281.9 ± 2.2 Ma and is the time of ore formation. Formation of the Cihai iron deposit is closely related to post-collisional magmatism and associated Cu–Ni–Au polymetallic mineralization in the eastern Tianshan.     

Arsenic behaviour in gold-ore mill tailings,Massif Central,France: hydrogeochemical study and investigation of in situ redox signatures

Historical Au-ore exploitation at the Chéni mine in the Massif Central, France, generated 525,000 tonnes of finely ground mill tailings deposited in a heap that has spread with time into three settling basins. The tailings, which are rich in quartz (80%), mica and clay minerals (10% of illite, smectite, kaolinite and chlorite), feldspars (5%) but poor in carbonates (<1%), also contain sulphides (around 5%, mainly pyrite and arsenopyrite). Arsenic content of the tailings is around 6 g kg. This paper describes the geochemistry of drainage waters, with special attention paid to in situ values of the three major redox couples, namely Fe(II)/Fe(III), As(III)/As(V) and S(IV)/S(VI). The water samples range from acidic and oxidized (pH 2.9, E_h +700 mV) to moderate pH and weakly reducing (pH 7.6, E_h 15 mV). The waters are rich in SO₄ and Ca and have variable As (0.05–95 mg L⁻¹) and Fe concentrations (0.07–141 mg L⁻¹). Reduced As(III) species predominate over As(V) species (As(III)/As(V) up to 21), whereas oxidized forms of Fe and S are favoured (Fe(II)/Fe(III) up to 0.5, and S(IV)/S(VI) up to 1).Thermodynamic calculations were performed with the PHREEQC and EQ3NR codes based on a revised As database to evaluate saturation indices (SI) of the waters in relation to the main minerals and define which redox couples control the redox state of the system. The important role of carbonates, though only present in small amounts, explains the acid buffering generated by the oxidation of sulphides for waters in the pH 7–7.5 range. Measured E_h appears to fall between the calculated E_h of the Fe(II)/Fe(III) couple and that of the As(III)/As(V) couple, illustrating redox disequilibrium.     

Native antimony in the Baogutu gold deposit (west Junggar,NW China): Its occurrence and origin

The Baogutu gold deposit, West Junggar (Xinjiang, NW China), is composed of quartz–sulfide veins and their stockworks and is hosted within an Early Carboniferous volcanic–sedimentary sequence. Three ore-forming paragenetic stages can be identified: coarse-grained quartz–sulfide vein (stage I), gold-bearing fine-grained quartz–sulfide vein (stage II), and native antimony-bearing calcite–sulfide veinlets (stage III). The estimated formation temperatures (approximately 360 to 220 °C), fS₂ (? 7 to ? 15 log units), and fO₂ (? 26 to ? 43 log units) decrease from stage I, through stage II, to stage III. The nature of the hydrothermal fluid changed from weakly acidic (pH: 5 to 6 at stage I) to alkaline (pH: > 7 at stage III).Two different occurrences of native antimony could be identified: one coexists with chalcopyrite and pyrrhotite, whereas the other occurs as isolate grains within calcite veins. Native antimony (up to 100 μm in size) contains minor amounts of As (2.0 to 2.7 wt.%); empirical formula Sb_0.95–0.96As_0.03–0.04. Decrease of temperature and fO₂ at high pH and low fS₂ conditions favored co-precipitation of native antimony–ullmannite assemblages and the decomposition of tetrahedrite. Native antimony crystallized later than the native gold, suggesting fractionation between Au and Sb during the hydrothermal evolution of the deposit.     

Mineralogical and geochemical investigations of the Mombi bauxite deposit,Zagros Mountains,Iran

The Mombi bauxite deposit is located in 165 km northwest of Dehdasht city, southwestern Iran. The deposit is situated in the Zagros Simply Fold Belt and developed as discontinuous stratified layers in Upper Cretaceous carbonates (Sarvak Formation). Outcrops of the bauxitic horizons occur in NW-SE trending Bangestan anticline and are situated between the marine neritic limestones of the Ilam and Sarvak Formations. From the bottom to top, the deposit is generally consisting of brown, gray, pink, pisolitic, red, and yellow bauxite horizons. Boehmite, diaspore, kaolinite, and hematite are the major mineral components, while gibbsite, goethite, anatase, rutile, pyrite, chlorite, quartz, as well as feldspar occur to a lesser extent. The Eh–pH conditions during bauxitization in the Mombi bauxite deposit show oxidizing to reducing conditions during the Upper Cretaceous. This feature seems to be general and had a significant effect on the mineral composition of Cretaceous bauxite deposits in the Zagros fold belt. Geochemical data show that Al₂O₃, SiO₂, Fe₂O₃ and TiO₂ are the main components in the bauxite ores at Mombi and immobile elements like Al, Ti, Nb, Zr, Hf, Cr, Ta, Y, and Th were enriched while Rb, Ba, K, Sr, and P were depleted during the bauxitization process. Chondrite-normalized REE pattern in the bauxite ores indicate REE enrichment (ΣREE = 162.8–755.28 ppm, ave. ∼399.36 ppm) relative to argillic limestone (ΣREE = 76.26–84.03 ppm, ave. ∼80.145 ppm) and Sarvak Formation (ΣREE = 40.15 ppm). The REE patterns also reflect enrichment in LREE relative to HREE. Both positive and negative Ce anomalies (0.48–2.0) are observed in the Mombi bauxite horizons. These anomalies are related to the change of oxidation state of Ce (from Ce³⁺ to Ce⁴⁺), ionic potential, and complexation of Ce⁴⁺ with carbonate compounds in the studied horizons. It seems that the variations in the chemistry of ore-forming solutions (e.g., Eh and pH), function of carbonate host rock as a geochemical barrier, and leaching degree of lanthanide-bearing minerals are the most important controlling factors in the distribution and concentration of REEs. Several lines of evidences such as Zr/Hf and Nb/Ta ratios as well as similarity in REE patterns indicate that the underlying marly limestone (Sarvak Formation) could be considered as the source of bauxite horizons. Based on mineralogical and geochemical data, it could be inferred that the Mombi deposit has been formed in a karstic environment during karstification and weathering of the Sarvak limy Formation.     

Subduction of a spreading ridge within the Bangong Co–Nujiang Tethys Ocean: Evidence from Early Cretaceous mafic dykes in the Duolong porphyry Cu–Au deposit,western Tibet

The intrusion of mafic dykes into a near-trench accretionary prism, and continental margin magmatism with characteristics that differ from those of adjacent arc magmatism, are direct manifestations of the subduction of a spreading ocean ridge and the formation of a slab window. In this paper, we investigated mafic dykes intruded into the accretionary prism that hosts the Duolong porphyry Cu–Au deposit (DCAD) of western Tibet. LA-ICP-MS analysis of U–Pb in zircon indicates that the dykes formed during the Early Cretaceous (126–127 Ma). The dykes are characterized by ε_Hf(t) values from + 2.44 to + 11.8. Twenty-nine mafic dyke samples were divided into three groups based on their locations and geochemical compositions: group I has Nb = 8.31–10.2 ppm, Nb/La = 0.71–1.20, and Nb/U = 21.4–37.9; group II has Nb = 40.5–52.6 ppm, Nb/La = 0.84–1.58, and Nb/U = 18.8–47.8; and group III has Nb = 65.7–105 ppm, Nb/La = 1.35–2.08, and Nb/U = 36.5–73.8. Group I is classified as Nb-enriched basalts (ENBs), whereas groups II and III are classified as high-Nb basalts (HNBs). Both the ENBs and HNBs were derived from an adakite-metasomatized mantle wedge that subsequently underwent crystallization of olivine and clinopyroxene. The compositional variations of the studied dykes resulted mainly from mantle source heterogeneity. The volume of the slab melts gradually increases from group I (ENBs) to group II (HNBs) and group III (HNBs), leading to gradually increasing incompatible element concentrations. Considering their geochemical characteristics and field relationships, as well as the unique characteristics of continental margin magmatism in the DCAD, we propose that the dykes emplaced in an extensional accretionary prism were derived from the northward subduction of a spreading ridge in the Bangong Co–Nujiang Tethys Ocean during the Early Cretaceous. The ridge subduction event was also responsible for the generation of coeval adakites, intermediate–felsic intrusions, the Maierze bimodal volcanic rocks as well as the metallogenesis of the DCAD.     

Origin of fluids in the Hetaoping Pb–Zn deposit,Baoshan–Narong–Dongzhi block metallogenic belt,Yunnan Province,SW China

The Hetaoping skarn type Pb–Zn deposit is located in the Baoshan–Narong–Dongzhi block metallogenic belt (BND belt), a belt between the Tengchong terrane and the Lanping basin. The deposit is hosted by marble of the upper Cambrian Hetaoping Formation and there are no outcrops of plutonic rocks present. This deposit is one of two large Pb–Zn deposits recently discovered in the BND belt. The Hetaoping deposit is a high Mn skarn. Four types of fluid inclusions were recognized in quartz from the deposit: vapor-rich inclusions (Type I), liquid-rich inclusions (Type II), pure vapor inclusions (Type III), and pure fluid inclusions (Type IV). The coexistence of Type I and Type III inclusions in Stage I (pre-ore stage) and Stage II (main ore stage) shows evidence of fluid boiling. Quartz-hosted fluid inclusions (Stage I and Stage II) display high homogenization temperatures and salinities (134–315 °C; 3.7–18.6 wt% NaCl equivalent) but calcite-hosted fluid inclusions in Stage III (post-ore stage) record lower homogenization temperatures and salinities (85–214 °C; 0.5–5.4 wt% NaCl equivalent). These data suggest a possible mixing between primary magmatic water and meteoric water. Based on chromatography data, the fluid inclusions in quartz contain abundant CO₂ and O₂ and subordinate CO, CH₄ and C₂H₂ + C₂H₄, suggesting an oxidizing environment. Based on their Na/K and Cl/SO₄ ratios, fluids contained in fluid inclusions are similar to volcanic spring waters. The low Na/K ratios (0.40–1.34) of the ore-forming fluids may have resulted from interaction with a deep alkaline intermediate-acid intrusion. Hydrogen and oxygen isotope determinations on quartz from different ore stages show low δ¹⁸O and δD values relative to VSMOW (−4.3‰ to 2.3‰; −109‰ to −91‰), indicating that the ore-forming fluids were diluted by external fluid sources as the skarn system cooled. Overall, geological and geochemical interpretations suggest that the Hetaoping deposit is a distal manganese skarn Pb–Zn deposit related to concealed intrusions.     

Highstands during Marine Isotope Stage 5: evidence from the Ironshore Formation of Grand Cayman,British West Indies

The Ironshore Formation on Grand Cayman is formed of six unconformity-bounded packages (units A–F). Units A, B, C, and D, known from the subsurface in the northeastern part of Grand Cayman, formed during Marine Isotope Stages (MIS) 11(?), 9, 7, and 5e, respectively. Unconformities at the tops of units A, B, and C are highlighted by terra rossa and/or calcrete layers. Strata in core obtained from wells drilled in George Town Harbour and exposed on the west part of Grand Cayman belong to unit D, and the newly defined units E and F. Corals from unit E yielded Th/U ages of ∼104 ka whereas conch shells from unit F gave ages of ∼84 ka. Unit E equates to MIS 5c whereas unit F developed during MIS 5a.Th/U dating of corals and conchs from the Ironshore Formation on the western part of Grand Cayman shows that unit D formed during the MIS 5e highstand whereas units E and F developed in association with highstands at 95–110 ka (MIS 5c) and 73–87 ka (MIS 5a). Unit E, ∼5 m thick in the offshore cores, is poorly represented in onshore exposures. Unit F, which unconformably overlies unit D at most localities, is formed largely of fossil-poor, cross-bedded ooid grainstones. The unconformity at the top of unit D, a marine erosional surface with up to 2.5 m relief, is not characterized by terra rossa or calcrete in the offshore cores or onshore exposures. Unit D formed with a highstand of +6 m asl, whereas units E and F developed when sea level was +2 to +5 asl and +3 to +6 m asl, respectively. Thus, the highstands associated with MIS 5e, 5c, and 5a were at similar elevations.     

Fluid inclusions and H–O–S–Pb isotope systematics of the Baishan porphyry Mo deposit in Eastern Tianshan,China

The Baishan porphyry Mo deposit formed in the Middle Triassic in Eastern Tianshan, Xinjiang, northwestern China. Mo mineralization is associated with the Baishan monzogranite and granite porphyry stocks, mainly presenting as various types of hydrothermal veinlets in alerted wall rocks, with potassic, phyllic, propylitic, and fluorite alteration. The ore-forming process can be divided into four stages: stage I K-feldspar–quartz–pyrite veinlets, stage II quartz–molybdenite ± pyrite veinlets, stage III quartz–polymetallic sulfide veinlets and stage IV barren quartz–calcite veins. Four types of fluid inclusions (FIs) can be distinguished in the Baishan deposit, namely, liquid-rich two-phase (L-type), vapor-rich two-phase (V-type), solid-bearing multi-phase (S-type) and mono-phase vapor (M-type) inclusions, but only the stage I quartz contains all types of FIs. The stages II and III quartz have three types of FIs, with exception of M-type. In stage IV quartz minerals, only the L-type inclusions can be observed. The FIs in quartz of stages I, II, III and IV are mainly homogenized at temperatures of 271–468 °C, 239–349 °C, 201–331 °C and 134–201 °C, with salinities of 2.2–11.6 wt.% NaCl equiv., 1.1–10.2 wt.% NaCl equiv., 0.5–8.9 wt.% NaCl equiv. and 0.2–5.7 wt.% NaCl equiv., respectively. The ore-forming fluids of the Baishan deposit are characterized by high temperature, moderate salinity and relatively reduced condition, belonging to a H₂O–NaCl ± CH₄ ± CO₂ system. Hydrogen and oxygen isotopic compositions of quartz indicate that the ore-forming fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials came predominantly from a deep-seated magma source from the lower continental crust. The Mo mineralization in the Baishan deposit is estimated to have occurred at a depth of no less than 4.7 km, and the decrease in temperature and remarkable transition of the redox condition (from alkalinity to acidity) of ore-forming fluids were critical for the formation of the Baishan Mo deposit.     

Genesis of the Fuxing porphyry Cu deposit in Eastern Tianshan,China: Evidence from fluid inclusions and C–H–O–S–Pb isotope systematics

The Fuxing porphyry Cu deposit is a recently discovered deposit in Eastern Tianshan, Xinjiang, northwestern China. The Cu mineralization is associated with the Fuxing plagiogranite porphyry and monzogranite, mainly presenting as various types of hydrothermal veins or veinlets in alerted wall rocks, with potassic, chlorite, phyllic, and propylitic alteration developed. The ore-forming process can be divided into four stages: stage I barren quartz veins, stage II quartz–chalcopyrite–pyrite veins, stage III quartz–polymetallic sulfide veins and stage IV quartz–calcite veins. Four types of fluid inclusions (FIs) can be distinguished in the Fuxing deposit, including hypersline (H-type), vapor-rich two-phase (V-type), liquid-rich two-phase (L-type), and trace amounts of pure vapor inclusions (P-type), but only the stage I quartz contains all types of FIs. The stages II and III quartz have two types of FIs, with exception of H- and P-types. In stage IV quartz minerals, only the L-type inclusions can be observed. The FIs in quartz of stages I, II, III and IV are mainly homogenized at temperatures of 357–518 °C, 255–393 °C, 234–322 °C and 145–240 °C, with salinities of 1.9–11.6 wt.% NaCl equiv., 1.6–9.6 wt.% NaCl equiv., 1.4–7.7 wt.% NaCl equiv. and 0.9–3.7 wt.% NaCl equiv., respectively. The ore-forming fluids of the Fuxing deposit are characterized by high temperature, moderate salinity and relatively oxidized condition. Carbon, hydrogen and oxygen isotopic compositions of quartz indicate that the ore-forming fluids were gradually evolved from magmatic to meteoric in origin. Sulfur and lead isotopes suggest that the ore-forming materials were derived from a deep-seated magma source. The Cu mineralization in the Fuxing deposit occurred at a depth of ~ 1 km, and the changes of oxygen fugacity, decompression boiling, and local mixing with meteoric water were most likely critical for the formation of the Fuxing Cu deposit.     

Seasonal variations of arsenic at the sediment–water interface of Poyang Lake,China

Arsenic species including arsenite, arsenate, and organic arsenic were measured in the porewaters collected from Poyang Lake, the largest freshwater lake of China. The vertical distributions of dissolved arsenic species and some diagenetic constituents [Fe(II), Mn(II), S(−II)] were also obtained in the same porewater samples in summer and winter. In sediments the concentration profiles of total As and As species bound to Fe–Mn oxyhydroxides and to organic matter were also determined along with the concentrations of Fe, Mn and S in different extractable fractions. Results indicate that, in the summer season, the concentrations of total dissolved As varying from 3.9 to 55.8 μg/L in sediments were higher than those (5.3–15.7 μg/L) measured in the winter season, while the concentrations of total As species in the solid phase varied between 10.97 and 25.32 mg/kg and between 7.84 and 30.52 mg/kg on a dry weight basis in summer and winter, respectively. Seasonal profiles of dissolved As suggest downward and upward diffusion, and the flux of dissolved As across the sediment–water interface (SWI) in summer and winter were estimated at 3.88 mg/m² a and 0.79 mg/m² a, respectively. Based on porewater profiles and sediment phase data, the main geochemical behavior of As was controlled by adsorption/desorption, precipitation and molecular diffusion. The solubility and migration of inorganic As are controlled by Fe–Mn oxyhydroxides in summer whereas they appear to be more likely controlled by both amorphous Fe–Mn oxyhydroxides and sulfides in winter. A better knowledge of the cycle of As in Poyang Lake is essential to a better management of its hydrology and for the environmental protection of biota in the lake.     

Mineralogy of low grade metamorphosed manganese sediments of the Urals: Petrological and geological applications

The paper describes mineralogy of the low grade metamorphosed manganese sediments, which occur in sedimentary complexes of the Pai Khoi Ridge and the Polar Urals and volcanosedimentary complexes of the Central and South Urals. The degree of metamorphism of the rocks studied corresponds to PT conditions of the prehnite–pumpellyite (deposits of Pai Khoi and Polar and South Urals) and green schist (deposits of the Central Urals) facies. One hundred and nine minerals were identified in the manganese-bearing rocks on the basis of optical and electron microscopy, X-ray diffraction, and microprobe analysis. According to the variations in the amount of major minerals of the manganese rocks of the Urals, they are subdivided on carbonate (I), oxide–carbonate–silicate (II), and oxide–silicate (III) types. Carbonates, various Mn^2 +-bearing silicates associated with oxides and carbonates, and braunite (Mn^3 +-bearing silicate) are the major Mn hosts in types I, II, and III, respectively. Because of the different oxidation state of Mn, the rocks of types I and II are termed as “reduced” and the rocks of type III, as “oxidized”. The formation of a certain mineralogical type of metamorphic assemblage is controlled by the content of organic matter in the primary sediments. The sequence type I → type II → type III reflects the decrease in the amount of organic matter in metalliferous sediments. Mineralogical data indicate that manganese in the primary sediments accumulated in a silicate form (MnSi gel, glass, etc). During diagenesis, the Mn–Si phase was transformed to neotokite with subsequent formation of caryopilite and further crystallization of pyroxmangite, rhodonite, tephroite, and other silicates due to reactions involving caryopilite. The hydrated Mn-silicates (caryopilite and/or friedelite) and the spatially associated parsettensite, stilpnomelane, and other minerals are the index minerals of the low grade metamorphism. Under PT conditions of prehnite–pumpellyite facies, nearly 70% of silicate minerals are hydrous. The metamorphosed Mn-bearing sediments are characterized by the low-temperature caryopilite (or tephroite-caryopilite-pyroxmangite ± rhodonite) and the high-temperature caryopilite-free (or tephroite-pyroxmangite ± rhodonite) facies. Their PT conditions correspond to zeolite and prehnite-pumpellyite (the low-temperature) and green schist and higher grade (the high-temperature) facies.