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1.
Computer-based reconstruction of the physicochemical conditions of formation of the Krasnov (16° N) and Ashadze (13° N) submarine systems in the Mid-Atlantic Ridge (MAR) has been performed using the equilibrium-thermodynamic approach to study samples from these sites. In the first case, a sphalerite-pyrite-barite association was considered, and in the second case, a sphalerite-pyrite association. In the modeling conducted, the composition of the sphalerite solid solution corresponding to the nonideal mixing of ZnS and FeS was used as a correlation parameter with the total composition of the Fe-Zn-Ba-S-H2O-NaCl-HCl hydrothermal system depending on temperature (200-300 °C) and a given pressure of 100 bar. The calculation results predict that at an iron content of 0.17-0.36 wt.% in sphalerite, the minimum formation temperatures of the equilibrium sphalerite-pyrite-barite association should correspond to the interval of 280-300 °C (Krasnov site). As the iron content in sphalerite increases to 4.15-13.28 wt.%, the occurrence of barite in the systems studied becomes impossible and the formation temperatures of the sphalerite-pyrite association become equal to or higher than 300 °C (Ashadze site).  相似文献   

2.
This work describes the in situ analysis of loparite [(Na,REE)Ti2O6], a perovskite group mineral with extremely low Rb/Sr ratios and high rare earth contents, by LA-(MC)-ICP-MS for the determination of U–Pb ages together with Sr and Nd isotopic composition. The reliability of these data were validated by analysis of a loparite standard by TIMS solution methods. Data are given for loparite from the Lovozero and Khibiny peralkaline complexes of the Kola Alkaline Province (Russia). For Lovozero loparite the Tera–Wasserburg intercept age for 15 loparites analysed is 373 ± 11 Ma, and the weighted 207Pb corrected 206Pb/238U age is 373 ± 2 Ma. For Khibiny loparite, the intercept age for 5 loparites analysed is 375 ± 10 Ma, and the weighted 207Pb corrected 206Pb/238U age is 374 ± 3 Ma. The common Pb compositions for Lovozero and Khibiny loparites are identical i.e. 207Pb/206Pb = 0.898 ± 0.009 and 0.898 ± 0.007, respectively. The 87Sr/86Sr initial ratios of Lovozero loparite range from 0.703552 to 0.703682 (av. 0.703611), and εNd (t370) from + 3.8 to + 4.4 (av. + 4.0). The 87Sr/86Sr initial ratios of Khibiny loparite range from 0.703560 to 0.703871, and εNd (t730) from + 4.0 to + 4.8. Our data indicate that in situ LA-(MC)-ICP-MS analysis of loparite provides accurate and precise estimates of the intrusion ages and isotopic composition of peralkaline rocks.  相似文献   

3.
Predicting pyrogenic carbon (PyC) or biochar stability from its precursor properties is critical for evaluating and managing terrestrial C stocks. Transmission mode Fourier transform infrared spectroscopy (FTIR) spectroscopy was compared with proximate analysis data and H/C and O/C for predicting C mineralization. PyC produced at 7 different temperatures from 6 different feedstocks, in addition to the original feedstock materials, was incubated for 3 yr at 30 °C in a sand matrix. A C debt or credit ratio was calculated by comparing the C remaining in the incubated PyC sample (accounting for the measured C lost during initial PyC production) to the C remaining in the incubated original feedstock. A value > 1 indicates that more C remains in the PyC than in the original feedstock (credit), while a value < 1 indicates a debt. After 3 yr, PyC produced at 300 °C lost significantly more C than higher temperature PyC material, but significant differences in C loss between PyC produced at temperatures ⩾ 350 °C were not detectable. The best predictor of C loss was a multiple linear regression model using the fractional FTIR signals at 816, 1048, 1374, 1424, 1460, 1590, 1700 and 2925 cm−1 as parameters (R2 0.80, p < 0.0001). After 3 yr, the C debt or credit ratio reached values significantly > 1 for all corn PyC samples and some bull, dairy and poultry PyC samples, resulting in net C credit, while all pine and oak PyC samples remained in debt. This C debt or credit ratio reveals that, depending on the timeline of interest, producing relatively low temperature PyC with less initial C loss can result in greater C savings than producing higher temperature PyC, even though the C remaining after exposure to higher pyrolysis temperatures is more stable.  相似文献   

4.
We review the crystallization of the iron meteorite chemical groups, the thermal history of the irons as revealed by the metallographic cooling rates, the ages of the iron meteorites and their relationships with other meteorite types, and the formation of the iron meteorite parent bodies. Within most iron meteorite groups, chemical trends are broadly consistent with fractional crystallization, implying that each group formed from a single molten metallic pool or core. However, these pools or cores differed considerably in their S concentrations, which affect partition coefficients and crystallization conditions significantly. The silicate-bearing iron meteorite groups, IAB and IIE, have textures and poorly defined elemental trends suggesting that impacts mixed molten metal and silicates and that neither group formed from a single isolated metallic melt. Advances in the understanding of the generation of the Widmanstätten pattern, and especially the importance of P during the nucleation and growth of kamacite, have led to improved measurements of the cooling rates of iron meteorites. Typical cooling rates from fractionally crystallized iron meteorite groups at 500–700 °C are about 100–10,000 °C/Myr, with total cooling times of 10 Myr or less. The measured cooling rates vary from 60 to 300 °C/Myr for the IIIAB group and 100–6600 °C/Myr for the IVA group. The wide range of cooling rates for IVA irons and their inverse correlation with bulk Ni concentration show that they crystallized and cooled not in a mantled core but in a large metallic body of radius 150±50 km with scarcely any silicate insulation. This body may have formed in a grazing protoplanetary impact. The fractionally crystallized groups, according to Hf–W isotopic systematics, are derived originally from bodies that accreted and melted to form cores early in the history of the solar system, <1 Myr after CAI formation. The ungrouped irons likely come from at least 50 distinct parent bodies that formed in analogous ways to the fractionally crystallized groups. Contrary to traditional views about their origin, iron meteorites may have been derived originally from bodies as large as 1000 km or more in size. Most iron meteorites come directly or indirectly from bodies that accreted before the chondrites, possibly at 1–2 AU rather than in the asteroid belt. Many of these bodies may have been disrupted by impacts soon after they formed and their fragments were scattered into the asteroid belt by protoplanets.  相似文献   

5.
The Jurassic–Lower Cretaceous aged carbonate sequence is widely exposed in the southern zone of Eastern Pontides. Aptian black bituminous limestone is found in the upper part of this sequence in the Kale area (Gümüşhane). This limestone contains faunal remains (e.g., gastropod, ostracod, characean stems and miliolid type benthic foraminifera) that indicate a freshwater, lacustrine depositional environment.The total organic carbon (TOC) values of the bituminous limestone samples range from 0.11–1.30% with an average TOC value of 0.54%. The hydrogen index (HI) varies from 119–448 mg HC/g TOC (average HI 298 mg HC/g TOC) indicating that the limestone contains gas prone as well as oil prone organic matter. Pyrolysis data prove that the organic matter content in the bituminous limestone consists of Type II kerogen. The average Tmax value for bituminous limestone samples is 438 °C (434–448 °C). Bitumen/TOC ratios for bituminous limestone are 0.05 and 0.04. The Tmax values and the ratios indicate that the bituminous limestone samples contain early mature to mature organic matter.Analysis of solvent extracts from the two richest bituminous limestones show a predominance of high carbon number (C26–C30) n-alkanes. The Pr/Ph ratio and CPI value are 1.34 and 0.96, respectively. C29 is the dominant sterane, with C29 > C27 > C28. The bituminous limestone samples have low C22/C21 ratios, high C24/C23 tricyclic terpane ratios and very low C31R/C30 hopane ratios (<0.25). These data are consistent with the bituminous limestones being deposited in a lacustrine environment.  相似文献   

6.
Black carbon (BC) is an important residue of wildfires in boreal forests, but its characteristics depend on its formation conditions. The objective of this study was to characterize the chemical and physical properties of BC produced under controlled laboratory conditions, while mimicking a gradient of wildfire severity. We used fuels originating from mosses, ericaceous shrubs and spruce trees, as they constitute the major types available in boreal forests. We varied the maximum temperature (MT) from 75 to 800 °C, the duration of charring from 0.5 to 24 h and the abundance of O2. BC properties were analyzed using elemental analysis and proximate analysis, solid state 13C nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscopy (SEM) and surface area (SA) analysis. MT was the most significant factor affecting both chemical and physical changes. Results from 13C NMR spectroscopy indicated that 350 °C was a threshold temperature, above which spectra became dominated by aromatic structures for all fuels. Charring duration affected BC composition at both low (250 °C for 12 h vs. 24 h) and high (600 °C for 0.5 h vs. 6 h) MT. The presence of O2 influenced BC composition mainly at low MT (250 °C) and resulted in accelerated alkyl C degradation, accompanied with a distinct decrease in yield. Results from the SA analysis and the SEM micrographs showed that fuel type influenced BC physical properties, with moss-derived BC presenting higher surface area and microporosity than BC of woody origin.  相似文献   

7.
Solid bituminous matter (SBM) typically occurs in the late hydrothermal assemblages of pegmatites of the Khibiny and Lovozero massifs, being confined to a microporous framework Ti-, Nb-, and Zr-silicates, which are sorbents of small molecules and efficient catalysts of the polymerization, reforming, and selective oxidation of organic matter. Bituminous matter from the pegmatites of the Lovozero Massif typically have elevated contents of aliphatic hydrocarbons, sulfur, and sodium, but are depleted in oxygen and trace elements. SBM from the pegmatites of the Khibiny Massif are depleted in sulfur and enriched in oxygen-bearing derivatives of polycyclic aromatic hydrocarbons. Being complexing agents for Th, REE, Ba, Sr, and Ca, they play a key role in the transfer and accumulation of Th and in the accumulation of alkali earth and rare earth elements during the hydrothermal stage of mineral formation. Oxidized SBM bearing rare and alkali earth elements are complex microheterogenous systems, which contain mineral (Th silicates, calcite, etc.), metalorganic (with REE, Ca, Sr, Ba), and predominantly organic phases formed by the exsolution of initial metalorganic material with decreasing temperature.  相似文献   

8.
Xincheng is a world-class orogenic-gold deposit hosted by the Early Cretaceous Guojialing granitoid in the Jiaodong Peninsula, eastern China. A zircon U–Pb age of 126 ± 1.4 Ma, together with previous data, constrain the emplacement of the Guojialing intrusion to 132–123 Ma. The granitoid underwent subsolidus ductile deformation at >500 °C following its intrusion. The small difference in age between the youngest zircon U–Pb age of unaltered granitoid (~123 Ma) and the ca. 120 Ma 40Ar/39Ar ages of sericite, associated with breccias and gold mineralization within it indicate initial rapid cooling from magmatic temperatures to those prevalent during brittle deformation and associated gold mineralization at ~220–300 °C. Evidence of a direct association between granitic magmatism and gold mineralization, such as at least localized near-magmatic depositional temperatures and metal zoning evident in undoubted intrusion-related gold deposits, is absent. The 40Ar/39Ar age of ~120 Ma coincides with the mineralization age of many other orogenic-gold deposits along the Jiaojia Fault. Sixteen zircon fission-track (ZFT) ages across the ore and alteration zones range from 112.9 ± 3.4 to 99.1 ± 2.7 Ma. The long period of cooling to the ~100 Ma ZFT closure temperatures recorded here suggests that ambient temperatures for hydrothermal alteration systems lasted to ~100 Ma, possibly because of their focus at Xincheng within the young Guojialing granitoid as it cooled more slowly below approximately 300 °C to 220 °C. However, the restricted number of auriferous ore stages, combined with the presence of cross-cutting gold-free quartz-carbonate veins, indicate that gold itself was only deposited over a restricted time interval at ~120 Ma, consistent with studies of orogenic gold deposits elsewhere. This highlights the complex interplay between magmatism, deformation and the longevity of hydrothermal systems that cause genetic controversies. Based on apatite fission-track (AFT) ages, the Xincheng gold deposit was then uplifted and exhumed to near the surface of the crust at 15 Ma, probably due to movement on the crustal-scale Tan-Lu Fault. Recognition of such exhumation histories along gold belts has conceptual exploration significance in terms of the probability of discovery of additional exposed or sub-surface gold ore bodies as discovery is as much a function of preservation as formation of the deposits.  相似文献   

9.
Dissolution rates of pressure solution (PS) for quartz aggregates in 0.002 M NaHCO3 solution were experimentally determined under low effective stress conditions of 0.42–0.61 MPa, and low temperatures of 25–45 °C. At temperatures of 25 °C, 35 °C, and 45 °C, the resultant silicon dissolution rates are 4.2 ± 1.2 × 10−15, 6.0 ± 1.0 × 10−15 and 7.8 ± 1.9 × 10−15 mol/cm2/s, respectively. Ratios between these dissolution rates and those of quartz sand at zero effective stress are 4.1 ± 1.2 at 25 °C, 3.0 ± 0.5 at 35 °C, and 2.4 ± 0.6 at 45 °C. As the uniaxial pressure was increased, the dissolution rate of PS also increased, though gradually decreased when the effective stress was kept constant. After the removal of stress, the dissolution rate was observed to increase once again. The activation energy of our PS experiments was determined to be approximately 24 kJ/mol, lower than the amount required for quartz sand dissolution to commence at zero effective stress. Our results clearly show that, even at such low temperature and effective stress, Si released into solution as a result of PS can be detected. This implies that experimental compaction of quartz aggregates can be measured even under such condition.  相似文献   

10.
The newly discovered Handagai skarn Fe–Cu deposit is located in the northern Great Xing'an Range of NE China and is hosted by the Ordovician Luohe Formation. The orebodies that form the deposit are generally concordant with the bedding within these sediments, and are spatially related to areas of skarn development. The Fe–Cu mineralization in this area records four stages of paragenesis, namely prograde skarn, retrograde skarn, quartz–sulfide, and quartz–carbonate stages. The Handagai deposit is a calcic skarn that is dominated by an andradite–diopside–epidote–actinolite assemblage. The mineralogy and geochemistry of the skarn indicate that it formed from a hydrothermal fluid that altered the carbonate units in this area to a garnet (And42–95Grs4–53) and pyroxene (Di71–78Hd22–29Jo0–2) bearing skarn. The epidote within the skarn has an epidote end-member composition, with the chlorite in the skarn dominantly Fe-rich, indicating that these minerals formed in an Fe-rich environment. The petrographic, microthermometric, and Raman spectroscopic analysis of fluid inclusions within garnet, epidote, actinolite, quartz, and calcite precipitated at different stages of formation of the Handagai deposit indicate that mineralization-related fluid inclusions are either liquid-rich two-phase H2O–NaCl (type I), gas-rich two-phase H2O–NaCl (type II), three-phase (liquid + vapor + solid) H2O–NaCl (type III), or CO2–H2O–NaCl inclusions (type IV). The early stages of mineralization are associated with all four types of inclusion, whereas the later stages of mineralization are only associated with type I and II inclusions. Inclusion homogenization temperatures vary between the four stages of mineralization (370 °C–530 °C and > 600 °C, 210 °C–290 °C, 190 °C–270 °C, and 150 °C–230 °C, from early to late, respectively), with salinities also varying between the earlier and later stages of mineralization (11–18 and > 45, 7–15, 6–9, and 3–7 wt.% NaCl equivalent (equiv.), respectively). The majority of the inclusions within the Handagai deposit have homogenization temperatures and salinities of 200 °C–350 °C and 4–14 wt.% NaCl equiv., respectively, indicating that this is a medium–high temperature and medium–low salinity type deposit. The fluid inclusions were trapped at pressures of 11 to 72 MPa, corresponding to depths of 0.4 to 2.9 km. The geology, mineralogy, geochemistry, and fluid inclusions microthermometry indicate that the Handagai deposit formed as a result of contact infiltration metasomatism, with the deposition of ore minerals resulting from a combination of factors that include boiling as a result of reduced pressure, cooling, and fluid mixing.  相似文献   

11.
Tannins account for a significant proportion of plant biomass and are likely to contribute to the residues formed by incomplete biomass combustion (black carbon, BC). Nonetheless, the molecular properties of thermally modified tannins have not been investigated in laboratory charring experiments. We applied conventional analytical pyrolysis–gas chromatography–mass spectrometry (Py–GC–MS) and thermally assisted hydrolysis and methylation (THM–GC–MS) to investigate the effects of heat treatment with a muffle furnace on the properties of condensed tannins (CT) from Corsican pine (Pinus nigra) needles. Py–GC–MS showed a decrease in the relative abundance of the 1,2,3-trihydroxybenzenes (pyrogallols) at ⩾300 °C and of the dihydroxybenzenes (mainly catechols) at ⩾350 °C due to dehydroxylation of the CT B ring. Further dehydroxylation led to formation of monohydroxybenzenes (phenols), which showed a strong enrichment between 350 and 400 °C and, at higher temperatures, to a series of monocyclic and polycyclic aromatics [benzene, alkyl benzenes and polycondensed aromatic hydrocarbons (PAHs)]. Degradation of the A ring could not be recognized via Py–GC–MS, probably because of the poor chromatographic behavior of 1,3,5-trihydroxybenzenes (phloroglucinols). The progressive dehydroxylation and eventual polycondensation of the CT B ring was corroborated using THM–GC–MS. In addition, with THM–GC–MS the thermal rearrangement of CT A rings at 300 °C and higher was inferred from the relative abundance of 1,3,5-trimethoxybenzenes (methylated phloroglucinol derivatives). These compounds were observed at moderate/high temperature (up to 450 °C) and can not be produced from THM of lignin, suggesting that they may be markers of CT in natural BC samples.  相似文献   

12.
Future climatic conditions may coincide with an increased potential for wildfires in grassland and forest ecosystems, whereby charred biomass would be incorporated into soils. Molecular changes in biomass upon charring have been frequently analysed with a focus on black carbon. Aliphatic and aromatic hydrocarbons, known to be liberated during incomplete combustion of biomass have been preferentially analysed in soot particles, whereas determinations of these compounds in charred biomass residues are scarce. We discuss the influence of increasing charring temperature on the aliphatic and aromatic hydrocarbon composition of crop grass combustion residues. Straw from rye, representing C3 grasses and maize, representing C4 grasses, was charred in the presence of limited oxygen at 300, 400 and 500 °C. Typical n-alkane distribution patterns with a strong predominance of long chain odd-numbered n-alkanes maximising at C31 were observed in raw straw. Upon combustion at 300 °C aliphatic hydrocarbons in char were dominated by sterenes, whereas at 400 °C sterenes disappeared and medium chain length n-alkanes, maximising around n-C20, with a balanced odd/even distribution were present. At a charring temperature of 500 °C n-alkane chain length shifted to short chain homologues, maximising at C18 with a pronounced predominance of even homologues. Even numbered, short chain n-alkanes in soils may thus serve as a marker for residues of charred biomass. Aromatic hydrocarbons indicate an onset of aromatization of biomass already at 300 °C, followed by severe aromatization upon incomplete combustion at 400–500 °C. The diagnostic composition of aliphatic and aromatic hydrocarbons from charred biomass affords potential for identifying residues from burned vegetation in recent and fossil soils and sediments.  相似文献   

13.
Most of the hydrothermal uranium (U) deposits from the European Hercynian belt (EHB) are spatially associated with Carboniferous peraluminous leucogranites. In the southern part of the Armorican Massif (French part of the EHB), the Guérande peraluminous leucogranite was emplaced in an extensional deformation zone at ca. 310 Ma and is spatially associated with several U deposits and occurrences. The apical zone of the intrusion is structurally located below the Pen Ar Ran U deposit, a perigranitic vein-type deposit where mineralization occurs at the contact between black shales and Ordovician acid metavolcanics. In the Métairie-Neuve intragranitic deposit, uranium oxide-quartz veins crosscut the granite and a metasedimentary enclave.Airborne radiometric data and published trace element analyses on the Guérande leucogranite suggest significant uranium leaching at the apical zone of the intrusion. The primary U enrichment in the apical zone of the granite likely occurred during both fractional crystallization and the interaction with magmatic fluids. The low Th/U values (< 2) measured on the Guérande leucogranite likely favored the crystallization of magmatic uranium oxides. The oxygen isotope compositions of the Guérande leucogranite (δ18Owhole rock = 9.7–11.6‰ for deformed samples and δ18Owhole rock = 12.2–13.6‰ for other samples) indicate that the deformed facies of the apical zone underwent sub-solidus alteration at depth with oxidizing meteoric fluids. Fluid inclusion analyses on a quartz comb from a uranium oxide-quartz vein of the Pen Ar Ran deposit show evidence of low-salinity fluids (1–6 wt.% NaCl eq.), in good agreement with the contribution of meteoric fluids. Fluid trapping temperatures in the range of 250–350 °C suggest an elevated geothermal gradient, probably related to regional extension and the occurrence of magmatic activity in the environment close to the deposit at the time of its formation. U-Pb dating on uranium oxides from the Pen Ar Ran and Métairie-Neuve deposits reveals three different mineralizing events. The first event at 296.6 ± 2.6 Ma (Pen Ar Ran) is sub-synchronous with hydrothermal circulations and the emplacement of late leucogranitic dykes in the Guérande leucogranite. The two last mineralizing events occur at 286.6 ± 1.0 Ma (Métairie-Neuve) and 274.6 ± 0.9 Ma (Pen Ar Ran), respectively. Backscattered uranium oxide imaging combined with major elements and REE geochemistry suggest similar conditions of mineralization during the two Pen Ar Ran mineralizing events at ca. 300 Ma and ca. 275 Ma, arguing for different hydrothermal circulation phases in the granite and deposits. Apatite fission track dating reveals that the Guérande granite was still at depth and above 120 °C when these mineralizing events occurred, in agreement with the results obtained on fluid inclusions at Pen Ar Ran.Based on this comprehensive data set, we propose that the Guérande leucogranite is the main source for uranium in the Pen Ar Ran and Métairie-Neuve deposits. Sub-solidus alteration via surface-derived low-salinity oxidizing fluids likely promoted uranium leaching from magmatic uranium oxides within the leucogranite. The leached out uranium may then have been precipitated in the reducing environment represented by the surrounding black shales or graphitic quartzites. As similar mineralizing events occurred subsequently until ca. 275 Ma, meteoric oxidizing fluids likely percolated during the time when the Guérande leucogranite was still at depth. The age of the U mineralizing events in the Guérande region (300–275 Ma) is consistent with that obtained on other U deposits in the EHB and could suggest a similar mineralization condition, with long-term upper to middle crustal infiltration of meteoric fluids likely to have mobilized U from fertile peraluminous leucogranites during the Late Carboniferous to Permian crustal extension events.  相似文献   

14.
In northwest Turkey, high-pressure metamorphic rocks occur as exotic blocks within the Çetmi mélange located on the south of the Biga Peninsula. Rutile chemistry and rutile thermometry obtained from the eclogite and associated garnet-mica schist in the Çetmi mélange indicate significant trace element behaviour of subducted oceanic crust and source-rock lithology of detrital rutiles. Cr and Nb contents in detrital rutile from garnet-mica schist vary from 355 to 1026 μg/g and 323 and 3319 μg/g, respectively. According to the Cr-Nb discrimination diagram, the results show that 85% of the detrital rutiles derived from metapelitic and 15% from metamafic rocks. Temperatures calculated for detrital rutiles and rutiles in eclogite range from 540 °C to 624 °C with an average of 586 °C and 611 °C to 659 °C with an average of 630 °C at P = 2.3 GPa, respectively. The calculated formation temperatures suggest that detrital rutiles are derived from amphibolite- and eclogite-facies metamorphic rocks. Amphibolite-facies rocks of the Kazdağ Massif could be the primary source rocks for the rutiles in the garnet-mica schist from the Çetmi mélange. Nb/Ta ratios of metapelitic and metamafic rutiles fall between 7–24 and 11–25, respectively. Nb/Ta characteristics in detrital rutiles may reflect a change in source-rock lithology. However, Nb/Ta ratios of rutiles in eclogite vary from 9 to 22. The rutile grains from eclogites are dominated by subchondritic Nb/Ta ratios. It can be noted that subchondritic Nb/Ta may record rutile growth from local sinks of aqueous fluids from metamorphic dehydration.  相似文献   

15.
The large, newly discovered Sharang porphyry Mo deposit and nearby Yaguila skarn Pb–Zn–Ag (–Mo) deposit reside in the central Lhasa terrane, northern Gangdese metallogenic belt, Tibet. Multiple mineral chronometers (zircon U–Pb, sericite 40Ar–39Ar, and zircon and apatite (U–Th)/He) reveal that ore-forming porphyritic intrusions experienced rapid cooling (> 100 °C/Ma) during a monotonic magmatic–hydrothermal evolution. The magmatic–hydrothermal ore-forming event at Sharang lasted ~ 6.0 Myr (~ 1.8 Myr for cooling from > 900 to 350 °C and ~ 4.0 Myr for cooling from 350 to 200 °C) whereas cooling was more prolonged during ore formation at Yaguila (~ 1.8 Myr from > 900 to 500 °C and a maximum of ~ 16 Myr from > 900 to 350 °C). All porphyritic intrusions in the ore district experienced exhumation at a rate of 0.07–0.09 mm/yr (apatite He ages between ~ 37 and 30 Ma). Combined with previous studies, this work implies that uplift of the eastern section of the Lhasa terrane expanded from central Lhasa (37–30 Ma) to southern Lhasa (15–12 Ma) at an increasing exhumation rate. All available geochronologic data reveal that magmatic–hydrothermal–exhumation activities in the Sharang–Yaguila ore district occurred within four periods of magmatism with related mineralization. Significant porphyry-type Mo mineralization was associated with Late Cretaceous–Eocene felsic porphyritic intrusions in the central Lhasa terrane, resulting from Neotethyan oceanic subduction and India–Asia continental collision.  相似文献   

16.
Seafloor sediment containing biogenic amino acids was heated with NaCl solutions at 50–200 °C for 240 h to investigate the dissolution process of amino acids and evaluate their stabilities under hydrothermal conditions. Dissolved amino acids in the combined phase (dissolved combined amino acids, DCAAs) and free phase (dissolved free amino acids, DFAAs) were rapidly released into the solution during heating. The amount of DCAAs in the solutions was 4–9 times higher than the amount of DFAAs at each temperature. When heated at ⩽ 100 °C, most of the total dissolved hydrolyzable amino acids (TDHAAs) were in the combined form (DCAAs/TDHAAs ratios > 0.9). The compositions of the DCAAs in solutions heated at ⩽ 100 °C were similar to that of the total hydrolyzable amino acids (THAAs) of the initial sediment, indicating that the DCAAs, which are derived from organisms and biodebris in the sediment, are barely altered during the hydrothermal reaction at these temperatures. On the other hand, the DCAAs/TDHAAs ratios were 0.72 and 0.57 at 150 and 200 °C, respectively, and the compositions of the DCAAs at 150 and 200 °C were significantly different from that of the initial THAAs. In addition, non-protein amino acids (β-alanine and γ-aminobutyric acid), which are sensitive biochemical indicators of the diagenetic alteration of natural organic matter, drastically increased to 80.9% of the DCAAs after heating at 200 °C. These results suggests that DCAAs are thermally unstable in the hydrothermal solutions at ⩾ 150 °C. These DCAA would be transformed into thermally stable geo-polymers such as humic-like substances and hydrolyzable kerogens.  相似文献   

17.
The Jílové deposit in the central part of the Bohemian Massif represents a vein to stockwork type of orogenic-type gold deposit. It is hosted by Neoproterozoic rocks of the Jílové Belt and by various magmatic dikes related to the ~ 355 to ~ 335 Ma Central Bohemian Plutonic Complex. The deposit is situated along the terrane boundary of the Teplá Barrandian and Moldanubian units.The deposit offered an exceptional opportunity to trace O, C, S and Sr stable isotope evolution of parent fluids based on combined mineralogical and geochemical study of carbonate, quartz, scheelite, and sulfide minerals, which represent six stages of mineralization, including the gold-bearing event.Stable isotope data and mineral and isotope thermometry indicate gangue and ore mineral formation between ~ 350 °C and < 100 °C, which can be divided into 6 stages. Scheelite-bearing assemblages (stages 2–3) precipitated at 292 ± 8 °C from a fluid with calculated values: δ18OSMOW = + 4.2 ± 0.5‰ and δ13CPDB = − 11 ± 1‰. Gold precipitation (stage 5) probably started at about 300 °C, but the major event probably occurred at 230 ± 30 °C from a fluid with more variable isotope values (δ18OSMOW = + 2.5 to + 5‰ and δ13CPDB = − 9 to − 13.5‰). The carbon speciation was characterized by predomination of dissolved CO2 (H2CO3ap.) in the fluids. Some gold, however, undoubtedly precipitated from bicarbonate dominated fluids even at < 120 °C.Extreme variations in the δ18O values of carbonate minerals, obtained from sampling profiles across individual veins with macroscopic gold, revealed severe thermal gradients during vein formation (~ 50 to ~ 100 °C difference of crystallization temperatures between the vein margin and core).The sulfur stable isotope composition of sulfide minerals indicates the dominant role of sulfur remobilization from Neoproterozoic rocks and stratiform mineralizations of the Jílové Belt by Variscan hydrothermal fluids. Similarly, the Sr-isotope composition of carbonates indicates both relatively primitive (87Sr/86Sr = 0.7055) and more evolved (87Sr/86Sr ~ 0.7090) fluid compositions, probably indicating fluid exchange with the Jílové Belt and the Central Bohemian Plutonic Complex rocks, respectively.Age determination of hydrothermal muscovite (related to stage 2) via 40Ar/39Ar indicated an age of 339.0 ± 1.5 Ma for the quartz veins. The mineralization is essentially coeval with the late intrusive phases of the Central Bohemian Plutonic Complex (i.e. the ultrapotassic suite) and with late-orogenic large-scale tectonic movements at the boundary between the two crustal terranes (Teplá-Barrandian and Moldanubian).Based on evaluation of the available age data on the hydrothermal and magmatic activity within the broader area of the Central Bohemian Plutonic Complex, we suggest two intervals of gold mineralization: 347 to 341 Ma and 340 to 337 Ma. The former interval overlaps with the intrusive activity of the Blatná high-K suite (granodiorite). The associated gold deposits (Mokrsko and Petráčkova hora) exhibit strong affiliation to the intrusion-related-gold-type deposit. The later interval overlaps with the ultrapotassic magmatism and is associated with more or less “classical” orogenic-gold-type deposits (Jílové, Bělčice, Libčice deposits).  相似文献   

18.
Apparent Re–Os ages of some magmatic sulfide ore deposits are older than the zircon and baddeleyite U–Pb ages which are interpreted as the formation age of the host intrusions. The Jinchuan Ni–Cu–PGE deposit of China, the world's third largest, is such a case. We report apparent Re–Os isochron ages of 1117 ± 67 Ma, 1074 ± 120 Ma and 867 ± 75 Ma with initial 187Os/188Os ratios of 0.120 ± 0.012, 0.162 ±0.017 and 0.235 ± 0.027 for disseminated ores, sulfides from the disseminated ores and massive ores from Jinchuan, respectively. Using these data and Re–Os ages from the literature, we find that the oldest apparent Re–Os age and lowest initial Os isotope ratio are from disseminated ores which contain small amounts of sulfide minerals, the highest initial Os isotope ratios and youngest apparent Re–Os ages, consistent with the zircon and baddeleyite U–Pb ages, are from massive ores containing 90–100 modal% sulfide, and net-textured ores with about 25 modal% sulfides yield apparent Re–Os ages and initial Os ratios intermediate between those of the disseminated and massive ores.Because Os diffusion between sulfides is inhibited by the intervening silicates even at high temperatures, re-equilibration did not occur in the disseminated ore and the samples retained the Os ratios of the contaminated magma, leading to geologically meaningless ages that are older than the formation age of the rocks. While Os-bearing sulfide minerals and magnetite show low closure temperatures of Os diffusion and the sulfide minerals in the massive ore are closely connected with each other, facilitating fast diffusion of Os, re-equilibration of Os was achieved during cooling of the ore from about 850 °C after the segregation to about 400 °C. Thus, an age corresponding to the formation time and an elevated initial Os ratio were yielded by the massive ore. Os isotopes in the net-textured ore behave in the way intermediate between the disseminated and massive ores. Pb isotope data support the Os results. Disseminated ores have heterogeneous Pb isotope ratios whereas Pb in the massive ores is more uniform, consistent with Pb isotopic equilibration in the massive ores, but not in the disseminated ores.  相似文献   

19.
《Applied Geochemistry》2006,21(6):977-992
Clayey formations are considered as suitable host rocks to develop a Deep Geological Repository (DGR) for nuclear wastes. A concrete ring, located between the clayey formation and the bentonite barrier, is needed as structural support for the galleries. This material will act as a source of alkaline fluids when the formation’s pore water saturates the system. This investigation evaluates the performance of the concrete-bentonite system by means of both geochemical codes and experimental results.A column made of compacted bentonite from La Serrata (Almería, Spain) (1.4 g/cm3, dry density) was held in contact with an ordinary Portland cement (OPC) mortar. Two alkaline solutions (Ca(OH)2 saturated and NaOH 0.25 M) were injected from the mortar’s side at 25, 60 and 120 °C. The permeability of the system and the effluent fluid composition were determined periodically. Finally, the solid phase was sampled and analyzed after 1 year of treatment.Ca(OH)2 saturated fluids does not alter the mineralogy over the experiment time scale. NaOH fluids produced minor changes at 60–25 °C but at 120 °C a thin tobermorite layer of 1.5 mm precipitates in the clay aggregate surfaces at the interface. After this layer, analcime nucleates in heterogeneous patches affecting the whole compacted bentonite probe (2 cm thickness). The use of the PHREEQC code thermodynamic approach predicts the mineralogical transformations. However, it is necessary to introduce kinetic laws and to consider the existence of stagnant zones in the model in order to simulate the heterogeneous spatial alteration observed.  相似文献   

20.
The thermobaric structure of the Himalayan Metamorphic Belt (HMB) has been constructed along the Kaghan Valley transect, Pakistan. The HMB in this valley represents mainly the Lesser Himalayan Sequence (LHS) and Higher Himalayan Crystallines (HHC). Mineral parageneses of 474 samples, from an approximately, 80-km traverse from southwest to northeast, were examined. Microprobe analyses were carried out to quantify the mineral composition. To determine the pressure–temperature (P–T) conditions, 65 thin sections (7 pelites from LHS and 25 pelites, 9 mafic rocks/amphibolites and 19 eclogites from HHC) were selected. Based on field observations and mineral paragenesis, low-grade to high-grade metapelites, show Barrovian-type progressive metamorphic sequence, with chlorite, biotite, garnet and staurolite zones in LHS and staurolite, kyanite and sillimanite zones in HHC. By using well-calibrated geothermobarometers, P–T conditions for pelitic and mafic rocks are estimated. P–T estimates for pelitic rocks from the garnet zone indicate a condition of 534 ± 17 °C at 7.6 ± 1.2 kbar. P–T estimates for rocks from the staurolite and kyanite zones indicate average conditions of 526 ± 17 °C at 9.4 ± 1.2 kbar and 657 ± 54 °C at 10 ± 1.6 kbar, respectively. P–T conditions for mafic rocks (amphibolites) and eclogites from HHC are estimated as 645 ± 54 °C at 10.3 ± 2 kbar and 746 ± 59 °C at 15.5 ± 2.1 kbar, respectively. The coesite-bearing ultrahigh-pressure (UHP) eclogites record a peak P–T condition of 757–786 °C at 28.6 ± 0.4 kbar and retrograde P–T conditions of 825 ± 59 °C at 18.1 ± 1.7 kbar.These results suggest that HMB show a gradual increase in metamorphic grade from southwest to northeast. The P–T conditions from Pelitic and adjacent mafic rocks having identical peak conditions in the same metamorphic zone, while the structural middle in HHC reached the highest P–T condition upto the UHP grade.  相似文献   

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