Peculiarities of the composition of volatile components in picroilmenites from Yakutian kimberlites of various ages (by gas chromatography—mass spectrometry)

The composition of volatile components in picroilmenites from Yakutian kimberlitic pipes of various ages (the Olivinovaya, Malokuonapskaya, and Udachnaya–East pipes) was studied for the first time by means of gas chromatography–mass spectrometry (GC-MS). It was shown that picroilmenites and olivines from same kimberlitic pipes contained volatile components of close composition, whereas these components were quite different in these minerals from different pipes. These features point to a common source and represent the specificity of the magma chamber formed under the pronounced influence of hydrocarbons with their derivates, as well as nitrogen-, chlorine-, and sulfur-containing compounds. The fraction of hydrocarbons and derivates in the composition of volatile matter is as high as 99%, including 9.7% of chlorine- and fluorinecontaining compounds.     

How jet is formed: An organic geochemical approach using pyrolysis gas chromatography–mass spectrometry

Six samples, including wood and jet-like material from the same mummified wood specimens, together with two ‘true’ jet samples, were studied using pyrolysis gas chromatography–mass spectrometry (Py-GC/MS) to obtain detailed insight into the process leading to the formation of jet. Based on morphological and chemical data obtained, the process of “jetification” is characterised by a rapid change when mummified wood is re-exposed to sunlight and aerobic conditions. The transformation from mummified wood to jet is probably caused by relatively small chemical changes, leading to extra linkages between the phenolic compounds and causing the structure to become much more rigid, which is reflected in increased inertness of the material at the macroscopic level.     

Emplacement ages and sources of kimberlites and related rocks in southern Africa: U–Pb ages and Sr–Nd isotopes of groundmass perovskite

Groundmass perovskite has been dated by LA-ICPMS in 135 kimberlites and related rocks from 110 localities across southern Africa. Sr and/or Nd isotopes have been analysed by LA-MC-ICPMS in a subset of these and integrated with published data. The age distribution shows peaks at 1,600–1,800, 1,000–1,200, 500–800 and 50–130 Ma. The major “bloom” of Group I kimberlites at ca 90 ± 10 Ma was preceded by a slow build-up in magmatic activity from ca 180 Ma. The main pulse of Group II kimberlites at 120–130 Ma was a distinct episode within this build-up. Comparison of the isotopic data with seismic tomography images suggests that metasomatized subcontinental lithospheric mantle (SCLM) with very low ε _Nd and high ⁸⁷Sr/⁸⁶Sr, (the isotopic signature of Group II kimberlites) was focused in low-Vs zones along translithospheric structures. Such metasomatized zones existed as early as 1,800 Ma, but were only sporadically tapped until the magmatic build-up began at ca 180 Ma, and contributed little to the kimberlitic magmas after ca 110 Ma. We suggest that these metasomatized volumes resided in the deep SCLM and that their low-melting point components were “burned off” by rising temperatures, presumably during an asthenospheric upwelling that led to SCLM thinning and a rise in the ambient geotherm between 120 and 90 Ma. The younger Group I kimberlites therefore rarely interacted with such SCLM, but had improved access to shallower volumes of differently metasomatized, ancient SCLM with low ⁸⁷Sr/⁸⁶Sr and intermediate ε _Nd (0–5). The kimberlite compositions therefore reflect the evolution of the SCLM of southern Africa, with metasomatic-enrichment events from as early as 1.8 Ga, through a major thermal and compositional change at ca 110 Ma, and the major kimberlite “bloom” around 90 Ma.     

Determination of fuel combustion product in airport runoff water samples using liquid–liquid extraction with gas chromatography–spectrometry

Determination of xenobiotics in samples of airport runoff water is both a complex and indispensable task due to an increasing threat resulting from the activities of numerous airports. The aim of this study was to develop, optimize, and validate a procedure based on liquid–liquid extraction (LLE) coupled with gas chromatography–mass spectrometry (GC–MS) for the determination of polycyclic aromatic hydrocarbons (PAHs). So far, no procedure was available that would ensure reliable data about concentration levels of these toxic pollutants in a new type of environmental samples, such as airport stormwater. The most difficult step in the analytical procedure used for the determination of fuel combustion products in airport stormwater samples is sample preparation. In this work, eight different protocols of sample preparation were tested. The evaluation of the LLE demonstrated that the best extraction conditions were as follows: dichloromethane (extraction solvent), solvent volume of 15 mL and sample volume of 250 mL. The percent recovery values ranged from 66 to 106 %, which shows that the LLE technique is a powerful method for extracting PAHs from airport runoff water samples with a complex matrix composition. Moreover, the developed procedure was characterized by satisfactory selectivity and a relatively low LOQ (0.17–0.52 μg/L). The procedure has been successfully applied to the analysis of stormwater samples collected from different sites at international airport in Poland. The procedure can thus be used as a tool for tracking the environmental fate of these compounds and for assessing the environmental effect of airports.     

On the problem of variability in the chemical composition of mud–volcanic waters: Evidence from the Yuzhno-Sakhalinsk mud volcano

The results of hydrogeochemical observations on the Yuzhno-Sakhalinsk mud volcano in 2010–2014 are considered. The chemical analysis of samples of mud–volcanic waters was carried out at various analytical centers, which is similar to the common situation where hydrochemical data for a volcano are obtained by different researchers. It is shown that the chemical composition of the mud–volcanic waters is relatively stable in time and space (for different gryphons of the volcano). This allows us to determine the characteristic range of hydrogeochemical indicators. For each year of observations, the coefficients of variation for the concentrations of Na, Mg, Ca, K, and HCO₃ mostly range from 10 to 30%. However, the concentrations analyzed in individual samples may differ significantly from each other. These natural variations are a likely source of errors in the interpretation of hydrochemical data. In addition, it is necessary to account for the specifics of mud–volcanic waters as an object of analytical chemical investigations.     

Collision-related genesis of the Sharang porphyry molybdenum deposit,Tibet: Evidence from zircon U–Pb ages,Re–Os ages and Lu–Hf isotopes

Sharang is a low-fluorine, calc-alkaline porphyry Mo deposit hosted mainly in a granite porphyry of a multi-stage plutonic complex in the northern Gangdese metallogenic belt, largely with stockwork and ribbon-textured mineralization. The observed age estimates suggest that the formation of the magmatic host complex (52.9–51.6 Ma) and the ore deposit itself (52.3 Ma) occurred during the main stage of the India–Asia collision. The host rocks are characterized by lower zircon ε_Hf(t) values than those of the pre-ore and post-ore rocks. This suggests that the Lhasa terrane basement might play an important role in the formation of Sharang ore-forming intrusions. In view of the framework of magmatic–metallogenic events we suggest that slab roll-back may have induced melting of juvenile crust and ancient continental complexes during the India–Asia collision. This proposal focuses exploration for additional molybdenum deposits on the collision zone.     

Contrasting sources of Late Paleozoic rhyolite magma in the Polish Lowlands: evidence from U–Pb ages and Hf and O isotope composition in zircon

International Journal of Earth Sciences - The Polish Lowlands, located southwest of the Teisseyre–Tornquist Zone, within Trans-European Suture Zone, were affected by bimodal, but dominantly...     

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...     

Re–Os isotopic ages of pyrite and chemical composition of magnetite from the Cihai magmatic–hydrothermal Fe deposit, NW China

The Eastern Tianshan Orogenic Belt of the Central Asian Orogenic Belt and the Beishan terrane of the Tarim Block, NW China, host numerous Fe deposits. The Cihai Fe deposit (>90 Mt at 45.6 % Fe) in the Beishan terrane is diabase-hosted and consists of the Cihai, Cinan, and Cixi ore clusters. Ore minerals are dominantly magnetite, pyrite, and pyrrhotite, with minor chalcopyrite, galena, and sphalerite. Gangue minerals include pyroxene, garnet, hornblende and minor plagioclase, biotite, chlorite, epidotite, quartz, and calcite. Pyrite from the Cihai and Cixi ore clusters has similar Re–Os isotope compositions, with ～14 to 62 ppb Re and ≤10?ppt common Os. Pyrrhotite has ～5 to 39 ppb Re and ～0.6 ppb common Os. Pyrite has a mean Re–Os model age of 262.3?±?5.6 Ma (n?=?13), in agreement with the isochron regression of ¹⁸⁷Os vs. ¹⁸⁷Re. The Re–Os age (～262 Ma) for the Cihai Fe deposit is within uncertainty in agreement with a previously reported Rb–Sr age (268?±?25 Ma) of the hosting diabase, indicating a genetic relationship between magmatism and mineralization. Magnetite from the Cihai deposit has Mg, Al, Ti, V, Cr, Co, Ni, Mn, Zn, Ga, and Sn more elevated than that of typical skarn deposits, but both V and Ti contents lower than that of magmatic Fe–Ti–V deposits. Magnetite from these two ore clusters at Cihai has slightly different trace element concentrations. Magnetite from the Cihai ore cluster has relatively constant trace element compositions. Some magnetite grains from the Cixi ore cluster have higher V, Ti, and Cr than those from the Cihai ore cluster. The compositional variations of magnetite between the ore clusters are possibly due to different formation temperatures. Combined with regional tectonic evolution of the Beishan terrane, the Re–Os age of pyrite and the composition of magnetite indicate that the Cihai Fe deposit may have derived from magmatic–hydrothermal fluids related to mafic magmatism, probably in an extensional rift environment.     

U�CPb isotopic ages and Hf isotope composition of zircons in Variscan gabbros from central Spain: evidence of variable crustal contamination

Ion microprobe U?CPb analyses of zircons from three gabbroic intrusions from the Spanish Central System (SCS) (Talavera, La Solanilla and Navahermosa) yield Variscan ages (300 to 305?Ma) in agreement with recent studies. Only two zircon crystals from La Solanilla massif gave slightly discordant Paleoproterozoic ages (1,848 and 2,010?Ma). Hf isotope data show a relatively large variation with the juvenile end-members showing ?Hf_i values as high as +3.6 to +6.9 and +1.5 to +2.9 in the Navahermosa and Talavera gabbros, respectively. These positive ?Hf_i values up to +6.9 might represent the composition of the subcontinental mantle which generates these SCS gabbros. This ?Hf_i range is clearly below depleted mantle values suggesting the involvement of enriched mantle components on the origin of these Variscan gabbros, and is consistent with previous whole-rock studies. The presence of zircons with negative ?Hf_i values suggest variable, but significant, crustal contamination of the gabbros, mainly by mixing with coeval granite magmas. Inherited Paleoproterozoic zircons of La Solanilla gabbros have similar trace element composition (e.g. Th/U ratios), but more evolved Hf-isotope signatures than associated Variscan zircons. Similar inherited ages have been recorded in zircons from coeval Variscan granitoids from the Central Iberian Zone. Granitic rocks have Nd model ages (T_DM) predominantly in the range of 1.4 to 1.6?Ga, suggesting a juvenile addition during the Proterozoic. However, Hf crustal model ages of xenocrystic Proterozoic zircons in La Solanilla gabbro indicate the presence of reworked Archean protoliths (T_DM2 model ages of 3.0 to 3.2?Ga) incorporated into the hybridized mafic magma.     

The Origin of the Early Proterozoic Kuandian Complex: Evidence from Geochemistry

The Kuandian Complex is scarcely preserved Early Proterozoic volcanic suite, formed2.3-2.4 Ga ago. It is located in an Early Proterozoic mobile belt bounded by the ArchaeanRangrim and Ryonggang Blocks of the northeastern Sino-Korean Craton. The Complex ismainly made up of amphibolites, gneisses, leucoleptite, leptite and layered granite. Petrologicaland geochemical studies show that the protoliths of the Complex are mainly assoctations ofbimodal volcanics and anorogenic granites. The Kuandian amphibolites are depleted in Nb, Ta,P and Ti, and enriched in LILE, e.g. K, Rb and Cs, with pronounced depletion of Sr relative toNd and Pb; La/Nb ratios are higher than 1(1.75 to 5.18). The trace element patterns of theamphibolites are similar to continental flood basalts formed by the Gondwana break-up, suchas those in South Karoo and Tasmania, which shows continental contamination. ε_(Nd) valuesranging from 0.70 to 1.94 of the Kuandian amphibolites and the relationships between Nb/Yband La/Yb suggest that contamination of basaltic magma happened in the mantle, rather thanalong the conduit. Isotope ratios of ~(208)Pb/~(204)Pb, ~(207)Pb/ ~(204)Pb, ~(206)Pb/~(204)Pb, ~(143)Nd/~(144)Ndand ~(87)Sr/~(86)Sr indicate that the magma was derived from a contaminated mantle source likeDMM or a mixture of DMM and EM2. The Kuandian Complex has Dupal anomaly, as is thecase with some continental basalts in the south hemisphere, e.g. in South Karoo and Tasmania.Petrochemical modelling proposes that the Kuandian gneiss, granite, and amphibolite camefrom the same parental magma, being products of strong fractional crystallization. Protoliths ofthe Kuandian Complex were formed in extensional tectonic setting during the transition fromcontinental crust to oceanic crust. The formation of the Kuandian Complex indicates that 2.3or 2.4 Ga ago tectonic evolution of the Sino-Korean craton was different from that of otherwell-studied Precambrian cratons, e.g. the North American shield, European platform andAustralian continent in that strong volcanic eruption resulted in its accretion. Besides, the con-taminated magma source with a Dupal anomaly for the Complex indicates that crust-mantleconvection whose scale was similar to that of the present plate tectonics had occurred at leastbefore the formation of the Kuandian Complex (2.3-2.4 Ga B.P).     

Source components of the Gran Canaria (Canary Islands) shield stage magmas: evidence from olivine composition and Sr–Nd–Pb isotopes

The Canary Island primitive basaltic magmas are thought to be derived from an HIMU-type upwelling mantle containing isotopically depleted (NMORB)-type component having interacted with an enriched (EM)-type component, the origin of which is still a subject of debate. We studied the relationships between Ni, Mn and Ca concentrations in olivine phenocrysts (85.6–90.0 mol.% Fo, 1,722–3,915 ppm Ni, 1,085–1,552 ppm Mn, 1,222–3,002 ppm Ca) from the most primitive subaerial and ODP Leg 157 high-silica (picritic to olivine basaltic) lavas with their bulk rock Sr–Nd–Pb isotope compositions (⁸⁷Sr/⁸⁶Sr = 0.70315–0.70331, ¹⁴³Nd/¹⁴⁴Nd = 0.51288–0.51292, ²⁰⁶Pb/²⁰⁴Pb = 19.55–19.93, ²⁰⁷Pb/²⁰⁴Pb = 15.60–15.63, ²⁰⁸Pb/²⁰⁴Pb = 39.31–39.69). Our data point toward the presence of both a peridotitic and a pyroxenitic component in the magma source. Using the model (Sobolev et al. in: Science 316:412–417, 2007) in which the reaction of Si-rich melts originated during partial melting of eclogite (a high pressure product of subducted oceanic crust) with ambient peridotitic mantle forms olivine-free reaction pyroxenite, we obtain an end member composition for peridotite with ⁸⁷Sr/⁸⁶Sr = 0.70337, ¹⁴³Nd/¹⁴⁴Nd = 0.51291, ²⁰⁶Pb/²⁰⁴Pb = 19.36, ²⁰⁷Pb/²⁰⁴Pb = 15.61 and ²⁰⁸Pb/²⁰⁴Pb = 39.07 (EM-type end member), and pyroxenite with ⁸⁷Sr/⁸⁶Sr = 0.70309, ¹⁴³Nd/¹⁴⁴Nd = 0.51289, ²⁰⁶Pb/²⁰⁴Pb = 20.03, ²⁰⁷Pb/²⁰⁴Pb = 15.62 and ²⁰⁸Pb/²⁰⁴Pb = 39.84 (HIMU-type end member). Mixing of melts from these end members in proportions ranging from 70% peridotite and 30% pyroxenite to 28% peridotite and 72% pyroxenite derived melt fractions can generate the compositions of the most primitive Gran Canaria shield stage lavas. Combining our results with those from the low-silica rocks from the western Canary Islands (Gurenko et al. EPSL 277:514–524, 2009), at least four distinct components are required. We propose that they are (1) HIMU-type pyroxenitic component (representing recycled ocean crust of intermediate age) from the plume center, (2) HIMU-type peridotitic component (ancient recycled ocean crust stirred into the ambient mantle) from the plume margin, (3) depleted, MORB-type pyroxenitic component (young recycled oceanic crust) in the upper mantle entrained by the plume, and (4) EM-type peridotitic component from the asthenosphere or lithosphere above the plume center.     

The First Finding of Sapphirine in Granulites of the Angara–Kan Block: Evidence of Ultra-High–Temperature Metamorphism in the SW Siberian Craton

This work reports the first discovery of sapphirine-bearing mineral parageneses in granulites of the Angara–Kan block, information on the mineral assemblage of rocks, and the mineral composition. Based on mineral geothermometers utilizing alumina content in orthopyroxene, reconstruction of the composition of ternary feldspar, and the titanium content in zircon, it was revealed that the peak temperatures of metamorphism reached 1100°C, after which the rocks underwent cooling under sub-isobaric conditions. It is assumed that the pulse of ultra-high-temperature metamorphism correlates with processes of extension and intraplate magmatism during the age interval of 1.78–1.75 Ga.     

The application of gas chromatography fingerprint technique to calculating oil production allocation of single layer in the commingled well

1Principle SincetheGCfingerprinttechniquewasfirstused tomonitortheproductionofoilfieldsbyAmericansci entists(KaufmanandAhmed,1990;Kaufmanetal.,1987)inthe1980s,manyresearchershavetentatively appliedthismethodinseveraloilfields(HeWenxiang etal.,1996;2001;WangZhengpingetal.,2000;ChenShijiaetal.,1999)andhaveachievedsatisfac toryresults.Butthereappearsomeobviousdeficien ciesinthecourseofexplorationanddevelopment.Takinganthraceneasinternalstandard,wecalculated theabsoluteconcentrationsoffingerp…     

Analyzing crude oils from the Junggar Basin (NW China) using comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (GC×GC-TOFMS)

As a new technology of analyzing crude oils, comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (GC×GC-TOFMS) has received much research attention. Here we present a case study in the Junggar Basin of NW China. Results show that the hydrocarbons, including saturates and aromatics, were all well-separated without large co-elution, which cannot be realized by conventional one-dimensional GC–MS. The GC×GC technique is especially effective for analyzing aromatics and low-to-middle-molecular-weight hydrocarbons, such as diamondoids. The geochemical characteristics of crude oils in the study area were investigated through geochemical parameters extracted by GC×GC-TOFMS, improving upon the understanding obtained by GC–MS. Thus, the work here represents a new successful application of GC×GC-TOFMS, showing its broad usefulness in petroleum geochemistry.     

Oxygen isotopic composition of coexisting minerals of sillimanite-hypersthene rocks from the Por’ya bay area: Evidence of fluid involvement in granulite-facies metamorphism

Hypersthene-garnet-sillimanite-quartz enclaves were studied in orthopyroxene-plagioclase and orthopyroxene-clinopyroxene crystalline schists and gneisses from shear zones exposed in Palenyi Island in the Early Proterozoic Belomorian Mobile Belt. Qualitative analysis of mineral assemblages indicates that these rocks were metamorphosed to the granulite facies (approximately 900°C and 10–11 kbar). Oxygen isotopic composition was determined in rock-forming minerals composing zones of the enclaves of various mineralogical and chemical composition. The closure temperatures of the isotopic systems obtained by methods of oxygen isotopic thermometry are close to the values obtained with mineralogical geothermometers (Grt-Opx and Grt-Bt) and correspond to the high-temperature granulite facies (860–900°C). Identified systematic variations in the δ¹⁸O values were determined in the same minerals from zones of different mineral composition. Inasmuch as these zones are practically in contact with one another, these variations in δ¹⁸O cannot be explained by the primary isotopic heterogeneity of the protolith. The model calculations of the extent and trend of the δ¹⁸O variations in minerals suggest that the only mechanism able to generate the zoning was fluid-rock interaction at various integral fluid/rock ratios in discrete zones. This demonstrates that a focused fluid flux could occur in lower crustal shear zones. The preservation of high-temperature isotopic equilibria of minerals testifies that the episode of fluid activity at the peak of metamorphism was very brief.     

Shared metamorphic histories of various Palaeoproterozoic granulites from Datong–Huai’an area,North China Craton (NCC): constraints from zircon U–Pb ages and petrology

ABSTRACT

Different tectonic interpretations have been proposed for the various spatially associated Palaeoproterozoic granulite-facies lithologies (metasedimentary rocks, metabasites, and felsic granulites) from north-central part of the North China Craton, which hinges primarily on controversies about metamorphic histories of these granulites, especially on the timing of peak metamorphism. Published data exhibit two controversial peak metamorphic ages of 1950–1900 Ma and 1850–1800 Ma. We report here LA-ICPMS U–Pb zircon ages of seven representative granulite-facies samples of different lithologies to constrain the timing of metamorphism, and then discuss their geological significance. Most zircon grains from these rocks display weak core-and-rim structures and yield two comparable group metamorphic ages of 1970–1900 Ma and 1880–1790 Ma, although their formation ages vary from Neoarchaean to Palaeoproterozoic. The older population metamorphic ages are interpreted to approximate timing of high-pressure granulite-facies metamorphism, and the younger population ages as the approximate timing of intermediate- to low-pressure granulite-facies metamorphism. Combined with recent petrological studies, we propose these granulites have shared metamorphic histories at least since ~1970–1900 Ma, and they are probably formed in one single metamorphic cycle in response to crustal-scale subduction–collision–exhumation processes involved in Palaeoproterozoic mobile belt.     

Mafic xenoliths in Proterozoic kimberlites from Eastern Dharwar Craton,India: Mineralogy and P–T regime

Mafic xenoliths of garnet pyroxenite and eclogite from the Wajrakarur, Narayanpet and Raichur kimberlite fields in the Archaean Eastern Dharwar Craton (EDC) of southern India have been studied. The composition of clinopyroxene shows transition from omphacite (3–6 wt% Na₂O) in eclogites to Ca pyroxene (<3 wt% Na₂O) in garnet pyroxenites. Some of the xenoliths have additional phases such as kyanite, enstatite, chromian spinel or rutile as discrete grains. Clinopyroxene in a rutile eclogite has an X_Mg value of 0.70, which is unusually low compared to the X_Mg range of 0.91–0.97 for all other samples. Garnet in the rutile eclogite is also highly iron-rich with an end member composition of Prp_26.5Alm_52.5Grs_14.7Adr_5.1TiAdr_0.3Sps_1.0Uv_0.1. Garnets in several xenoliths are Cr-rich with up to 8 mol% knorringite component. Geothermobarometric calculations in Cr-rich xenoliths yield different P–T ranges for eclogites and garnet pyroxenites with average P–T conditions of 36 kbar and 1080 °C, and 27 kbar and 830 °C, respectively. The calculated P–T ranges approximate to a 45 mW m^?2 model geotherm, which is on the higher side of the typical range of xenolith/xenocryst geotherms (35–45 mW m^?2) for several Archaean cratons in the world. This indicates that the EDC was hotter than many other shield regions of the world in the mid-Proterozoic period when kimberlites intruded the craton. Textural and mineral chemical characteristics of the mafic xenoliths favour a magmatic cumulate process for their origin as opposed to subducted and metamorphosed oceanic crust.