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1.
Temporal variation of PM10 using 2-year data (January, 2007–December, 2008) of Delhi is presented. PM10 varied from 42 to 200 μg m−3 over January to December, with an average 114.1 ± 81.1 μg m−3. They are comparable with the data collected by Central Pollution Control Board (National Agency which monitors data over the entire country in India) and are lower than National Ambient Air Quality (NAAQ) standard during monsoon, close to NAAQ during summer but higher in winter. Among CO, NO2, SO2, rainfall, temperature, and wind speed, PM10 shows good correlation with CO. Also, PM10, PM2.5, and PM1 levels on Deepawali days when fireworks were displayed are presented. In these festive days, PM10, PM2.5, and PM1 levels were 723, 588, and 536 μg m−3 in 2007 and 501, 389, and 346 μg m−3 in 2008. PM10, PM2.5, and PM1 levels in 2008 were 1.5 times lower than those in 2007 probably due to higher mixing height (446 m), temperature (23.8°C), and winds (0.36 ms−1).  相似文献   

2.
The intermetallic compound Ni3Au and Au-Ni solid solutions (native nickel Au and Au-bearing native Ni) were found in the contact metamorphosed metalliferous sediments of the Triassic chert formation in Sikhote-Alin. The metalliferous rocks are characterized by high contents of Au, Ag, and PGE, as well as the presence of diverse minerals of precious metals. Nickel gold (Au0.91-0.88 Ni0.09-0.12) is found as grains and crystals (3 to 4 im in size) in Au-bearing cherts with hematite, which are conventionally defined as “itabir-ites” and in the altered siliceous rocks of the Dal’nerechensky district (the upper reaches of the Gornya River). The nickel gold is associated with copper Au, pure native Au (Au1.00), and Au-Ag and Au-Ag-Pb solid solutions (Au0.86/0.84Ag0.14_0.16 and Au0.78Ag0.19Pb0.03, respectively). The Au-bearing Ni is found in the metamorphosed carbonaceous mudstones and Au-bearing “itabirites” of the Shirokopadninsky area (Olgin-sky district). The Au content varies from 6.09 wt % (Ni0.98Au0.02) to 11.30 wt % (Ni0.96Au0.04) in some Au-bearing Ni grains (about 10—15 im in diameter) taken from the metamorphosed mudstones. The grains of Au-bearing Ni (Co0.001_0.00Au00.2 - 0.17 Ni 0.98_0.83) in the “itabirites” are also characterized by their heterogeneous composition and the fine impregnation of the Ni3 Au intermetallic compound (Ni2.99Au1.01 based on the microprobe analysis).  相似文献   

3.
The thermal behaviour of β-anhydrite CaSO4 has been investigated to 1,263 K in-situ real-time using laboratory parallel-beam X-ray powder diffraction data. The cell parameters expanded anisotropically, the c axis being the “softest”. This behaviour is due to the deformation of the CaO8 polyhedron. In fact the two longest, independent, Ca–O bond distances show a significant component along the z direction.  相似文献   

4.
BEA  F. 《Journal of Petrology》1996,37(3):521-552
A systematic study with laser ablation—ICP-MS, scanningelectron microscopy and electron microprobe revealed that 70–95wt% of REE (except Eu), Y, Th and U in granite rocks and crustalprotoliths reside within REEYThU-rich accessories whose nature,composition and associations change with the rock aluminosity.The accessory assemblage of peraluminous granites, migmatitesand high-grade rocks is composed of monazite, xenotime (in low-Cavarieties), apatite, zircon, Thorthosilicate, uraninite andbetafite-pyrochlore. Metaluminous granites have allanite, sphene,apatite, zircon, monazite and Thorthosilicaie. Peralkaline graniteshave aeschinite, fergusonite, samarskite, bastnaesite, fluocerite,allanite, sphene, zircon, monazite, xenotime and Th-orthosilicate.Granulite-grade garnets are enriched in Nd and Sm by no lessthan one order of magnitude with respect to amphibolite-gradegarnets. Granulitegrade feldspars are also enriched in LREEwith respect to amphibolite-grade feldspars. Accessories causenon-Henrian behaviour of REE, Y, Th and U during melt—solidpartitioning. Because elevated fractions of monazite, xenotimeand zircon in common migmatites are included within major minerals,their behaviour during anatexis is controlled by that of theirhost. Settling curves calculated for a convecting magma showthat accessories are too small to settle appreciably, beingseparated from the melt as inclusions within larger minerals.Biotite has the greatest tendency to include accessories, therebyindirectly controlling the geochemistry of REE, Y, Th and U.We conclude that REE, Y, Th and U are unsuitable for petrogeneticalmodelling of granitoids through equilibrium-based trace-elementfractionation equations. KEY WORDS: accessory minerals; geochemical modelling; granitoids; REE, Y, Th, U  相似文献   

5.
Motivated by the rapid increase in atmospheric CO2 due to human activities since the Industrial Revolution, and the climate changes it produced, the world’s concerned scientific community has made a huge effort to investigate the global carbon cycle. However, the results reveal that the global CO2 budget cannot be balanced, unless a “missing sink” is invoked. Although numerous studies claimed to find the “missing sink”, none of those claims has been widely accepted. This current study showed that alkaline soil on land are absorbing CO2 at a rate of 0.3–3.0 μmol m−2 s−1 with an inorganic, non-biological process. The intensity of this CO2 absorption is determined by the salinity, alkalinity, temperature and water content of the saline/alkaline soils, which are widely distributed on land. Further studies revealed that high salinity or alkalinity positively affected the CO2 absorbing intensity, while high temperature and water content had a negative effect on the CO2 absorbing intensity of these soils. This inorganic, non-biological process of CO2 absorption by alkaline soils might have significant implications to the global carbon budget accounting.  相似文献   

6.
The rapid urbanization, industrialization, modernization, and the frequent Middle Eastern dust storms have negatively impacted the ambient air quality in Bahrain. The objective of this study is to identify the most critical atmospheric air pollutants with emphasis on their potential risk to health based on calculated AQI (air quality index) values using EPA approach. The air quality datasets of particulate matters (PM10 and PM2.5), ozone (O3), sulfur dioxide (SO2), nitrogen dioxide (NO2), and carbon monoxide (CO) were measured in January 2012 and August 2012 using five mobile air quality monitoring stations located at different governorates. The results of this study demonstrated that PM10 and PM2.5 are the most critical air pollutants in Bahrain with PM2.5 prevailing during January 2012 and PM10 prevailing during August 2012. The corresponding AQI categories were utilized to evaluate spatial variability of particulate matters in five governorates. The impact of meteorological factors such as ambient air temperature, wind speed, relative humidity, and total precipitation on ambient air quality were discussed. The analysis demonstrated that the highest PM10 concentrations were observed in the Northern Governorate while the highest PM2.5 concentrations were observed in the Capital, Central, and Northern Governorates during August 2012. It was observed that the levels of PM2.5 pollution were higher within proximity of the industrial zone. The results suggested that the average PM2.5/PM10 ratio in August 2012 was lower than in January 2012 due to the Aeolian processes. This study concludes that higher wind speed, total precipitation, relative humidity rates, and lower ambient air temperature in January 2012 assisted with the dissipation of particulate matter thus lowering the pollution levels of both PM10 and PM2.5 in comparison to August 2012.  相似文献   

7.
The Proterozoic Deadhorse Creek volcaniclastic breccia complex was emplaced in Archean metasedimentary and metavolcanic rocks of the Schreiber-White River greenstone belt adjacent to the Proterozoic Coldwell alkaline complex. The western sub-complex of the Deadhorse Creek breccia consists of metasomatically-altered breccia, a U-Be-Zr-rich main mineralized zone and a Zr-Y-Th-rich carbonate vein. The main mineralized zone is enriched in beryllium, thorium, uranium, first and second row transition elements, and rare earth elements. The major minerals present include: albite; potassium feldspar; quartz; calcite; apatite; and phenakite. Accessory minerals include: aegirine-jervisite; aegirine-natalyite; allanite; barite; barylite; coffinite; Ca-Mn-silicate; magnetite; monazite-(Ce); niobian vanadian rutile; pyrite; thorite; thorogummite; thortveitite; uraninite; vanadian crichtonite; xenotime-(Y); zircon and hydrated zircon; and zircon-thorite-coffinite solid solutions. The carbonate vein consists of dolomite-ankerite and calcite with accessory zircon, xenotime, and monazite. Barite, baotite and Ba-rich feldspars, were formed during metasomatism of the earlier-formed and genetically-unrelated volcaniclastic breccia adjacent to the main mineralized zone. The complex mineral assemblage of the fault-controlled main mineralized zone is considered to have formed in three stages. An initial emplacement of a “granitic” melt/fluid was followed by introduction of CO2-bearing Cr-Nb-V-Ti-enriched alkaline fluids. The latter reacted with minerals which had crystallized from the “granitic” melt/fluid to produce the exotic V-, Sc- and Nb-bearing mineral assemblage. Subsequently, a supergene suite of minerals, consisting principally of calcite, thorogummite, hollandite and tyuyamanite, formed during post-Pleistocene alteration was superimposed onto the pre-existing Proterozoic age mineral assemblage. The major mineralogy of the main mineralized zone is essentially ‘granitic” and the melts/fluids are considered to be derived from an A-type granite source. However, the Deadhorse Creek mineralization is older (1129±6 Ma) than the A-type quartz syenites of the adjacent Coldwell complex (1108±1 Ma) which are the nearest potential sources of such melts. Thus, the source of the “granitic” melt together with that of the Cr-Nb-V-Ti-bearing alkaline fluids remains enigmatic.  相似文献   

8.
Quaternary basalts in the Cerro del Fraile area contain two types of mantle xenoliths; coarse-grained (2–5 mm) C-type spinel harzburgites and lherzolites, and fine-grained (0.5–2 mm) intensely metasomatized F-type spinel lherzolites. C-type xenoliths have high Mg in olivine (Fo = 90–91) and a range in Cr# [Cr/ (Cr + Al) = 0.17–0.34] in spinel. Two C-type samples contain websterite veinlets and solidified patches of melt that is now composed of minute quenched grains of plagioclase + Cr-spinel + clinopyroxene + olivine. These patches of quenched melts are formed by decompression melting of pargasitic amphibole. High Ti contents and common occurrence of relic Cr-spinel in the quenched melts indicate that the amphibole is formed from spinel by interaction with the Ti-rich parental magma of the websterite veinlets. The fO2 values of these two C-type xenoliths range from ΔFMQ −0.2 to −0.4, which is consistent with their metasomatism by an asthenospheric mantle-derived melt. The rest of the C-type samples are free of “melt,” but show cryptic metasomatism by slab-derived aqueous fluids, which produced high concentrations of fluid-mobile elements in clinopyroxenes, and higher fO2 ranging from ΔFMQ +0.1 to +0.3. F-type lherzolites are intensely metasomatized to form spinel with low Cr# (∼0.13) and silicate minerals with low MgO, olivine (Fo = ∼84), orthpyroxene [Mg# = Mg/(Mg + ΣFe) = ∼0.86] and clinopyroxene (Mg# = ∼0.88). Patches of “melt” are common in all F-type samples and their compositions are similar to pargasitic amphibole with low TiO2 (<0.56 wt%), Cr2O3 (<0.55 wt%) and MgO (<16.3 wt%). Low Mg# values of silicate minerals, including the amphibole, suggest that the metasomatic agent is most likely a slab melt. This is supported by high ratios of Sr/Y and light rare earth elements (REE)/heavy REE in clinopyroxenes. F-type xenoliths show relatively low fO2 (ΔFMQ −0.9 to −1.1) compared to C-type xenoliths and this is explained by the fusion of organic-rich sediments overlying the slab during the slab melt. Trench-fill sediments in the area are high in organic matter. The fusion of such wet sediments likely produced CH4-rich fluids and reduced melts that mixed with the slab melt. High U and Th in bulk rocks and clinopyroxene in F-type xenoliths support the proposed interpretation.  相似文献   

9.
We present results from low-temperature heat capacity measurements of spinels along the solid solution between MgAl2O4 and MgCr2O4. The data also include new low-temperature heat capacity measurements for MgAl2O4 spinel. Heat capacities were measured between 1.5 and 300 K, and thermochemical functions were derived from the results. No heat capacity anomaly was observed for MgAl2O4 spinel; however, we observe a low-temperature heat capacity anomaly for Cr-bearing spinels at temperatures below 15 K. From our data we calculate standard entropies (298.15 K) for Mg(Cr,Al)2O4 spinels. We suggest a standard entropy for MgAl2O4 of 80.9 ± 0.6 J mol−1 K−1. For the solid solution between MgAl2O4 and MgCr2O4, we observe a linear increase of the standard entropies from 80.9 J mol−1 K−1 for MgAl2O4 to 118.3 J mol−1 K−1 for MgCr2O4.  相似文献   

10.
 This paper uses the geochemistry of primitive mafic lavas from the Rungwe volcanic province (southwestern Tanzania) to infer the source mineralogy and melting history. Post-Miocene mafic lavas from Rungwe include alkali basalts, basanites, nephelinites and picrites with up to 18.9 wt% MgO; nephelinites (>13.5% normative nepheline) are restricted to Kiejo volcano in the southern portion of the province. Rungwe lavas differ from most Western Rift volcanics in that they are not unusually potassic (K2O/Na2O ca. 0.40). Sparsely phyric mafic lavas contain phenocrysts and xenocrysts of plagioclase (An82–90), clinopyroxene (4.5–9.5 wt% Al2O3), and olivine (Fo79–88); one basanite contains a 1 mm xenocryst of apatite included in magnesian clinopyroxene. All samples have high abundances of incompatible elements (e.g., 0.7–2.2 wt% P2O5) and are enriched in REE relative to HFSE (Hf, Zr, Ti, Y), Cs, Ba, and K. Some incompatible element ratios are constant throughout the Rungwe suite (e.g., Zr/Nb, Sr/Ce, K/Rb), but other ratios are extremely variable and exceed the range measured in global Ocean Island Basalts (OIB) (e.g., Ba/Nb, Sm/Zr, La/Nb, Pb/Ce, Nb/U). The range in degree of silica saturation, and its excellent correlation with P2O5/Al2O3, indicate that the Rungwe suite records variable degrees of melting. Variations of individual incompatible trace element abundances in nephelinite and basanite samples suggest that the source contains metasomatic amphibole, ilmenite, apatite, and zircon. The Rungwe suite is interpreted as a series of low-percentage melts of CO2-rich peridotite at pressures that span the garnet-spinel transition. A geochemical comparison of Rungwe samples to lavas from other Western Rift volcanic centers requires that the source mineralogy varies along the rift axis, although each province is underlain by metasomatized peridotite. The incompatible trace element signatures of Western Rift lavas indicate that the source area is typically homogeneous on the scale of individual volcanoes, although lavas from each volcano reflect a range in degree of melting. Significantly, volcanoes with distinct geochemistry are always separated by major rift faults, suggesting that volcanic and tectonic surface features may correspond to metasomatic provinces within the subcontinental lithospheric mantle. Received: 30 May 1994 / Accepted: 5 April 1995  相似文献   

11.
A holistic study of the composition of the basalt groundwaters of the Atherton Tablelands region in Queensland, Australia was undertaken to elucidate possible mechanisms for the evolution of these very low salinity, silica- and bicarbonate-rich groundwaters. It is proposed that aluminosilicate mineral weathering is the major contributing process to the overall composition of the basalt groundwaters. The groundwaters approach equilibrium with respect to the primary minerals with increasing pH and are mostly in equilibrium with the major secondary minerals (kaolinite and smectite), and other secondary phases such as goethite, hematite, and gibbsite, which are common accessory minerals in the Atherton basalts. The mineralogy of the basalt rocks, which has been examined using X-ray diffraction and whole rock geochemistry methods, supports the proposed model for the hydrogeochemical evolution of these groundwaters: precipitation + CO2 (atmospheric + soil) + pyroxene + feldspars + olivine yields H4SiO4, HCO3 −, Mg2+, Na+, Ca2+ + kaolinite and smectite clays + amorphous or crystalline silica + accessory minerals (hematite, goethite, gibbsite, carbonates, zeolites, and pyrite). The variations in the mineralogical content of these basalts also provide insights into the controls on groundwater storage and movement in this aquifer system. The fresh and weathered vesicular basalts are considered to be important in terms of zones of groundwater occurrence, while the fractures in the massive basalt are important pathways for groundwater movement.  相似文献   

12.
Trace element distribution in Central Dabie eclogites   总被引：16，自引：0，他引：16  
Coesite-bearing eclogites from Dabieshan (central China) have been studied by ion microprobe to provide information on trace element distributions in meta-basaltic mineral assemblages during high-pressure metamorphism. The primary mineralogy (eclogite facies) appears to have been garnet and omphacite, usually with coesite, phengite and dolomite, together with high-alumina titanite or rutile, or both titanite and rutile; kyanite also occurs occasionally as an apparently primary phase. It is probable that there was some development of quartz, epidote and apatite whilst the rock remained in the eclogite facies. A later amphibolite facies overprint led to partial replacement of some minerals and particularly symplectitic development after omphacite. They vary from very fine-grained dusty-looking to coarser grained Am + Di + Pl symplectites. The eclogite facies minerals show consistent trace element compositions and partition coefficients indicative of mutual equilibrium. Titanite, epidote and apatite all show high concentrations of REE relative to clinopyroxene. The compositions of secondary (amphibolite facies) minerals are clearly controlled by local rather than whole-rock equilibrium, with the composition of amphibole in particular depending on whether it is replacing clinopyroxene or garnet. REE partition coefficients for Cpx/Grt show a dependence on the Ca content of the host phases, with D REE Cpx/Grt decreasing with decreasing D Ca . This behaviour is very similar to that seen in mantle eclogites, despite differences in estimated temperatures of formation of 650–850 °C (Dabieshan) and 1000–1200 °C (mantle eclogites). With the exception of HREE in garnet, trace elements in the eclogites are strongly distributed in favour of minor or accessory phases. In particular, titanite and rutile strongly concentrate Nb and Zr, whilst LREE–MREE go largely into epidote, titanite and apatite. If these minor/accessory minerals behave in a refractory manner during melting or fluid mobilisation events and do not contribute to the melt/fluid, then the resultant melts and fluids will be strongly depleted in LREE–MREE. Received: 11 February 1999 / Accepted: 31 January 2000  相似文献   

13.
Single-crystal polarized Raman spectra (3,000–4,000 cm−1 at 3 ≤ T ≤ 300 K) were measured for synthetic alkali-free and natural beryl, Be2Al3Si6O18·xH2O, to determine the behavior of H2O molecules of both Type I and Type II in the cavities. At low temperature, the H2O molecules of Type I displace from the center of cavity and give rise to very weak hydrogen bonding with the host lattice. The H2O Type I translational motion is characterized by substantial anharmonicity and looks like a motion of “a particle in the box” with a frequency of 6.3 cm−1. Water Type II is characterized by a free rotation with respect to the C 2 molecule axis, and it makes possible the water nuclear isomers (i.e. ortho- and para-) to be observed at low temperature.
Boris KolesovEmail:
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14.
Geologic storage of CO2 is expected to produce plumes of large areal extent, and some leakage may occur along fractures, fault zones, or improperly plugged pre-existing wellbores. A review of physical and chemical processes accompanying leakage suggests a potential for self-enhancement. The numerical simulations presented here confirm this expectation, but reveal self-limiting features as well. It seems unlikely that CO2 leakage could trigger a high-energy run-away discharge, a so-called “pneumatic eruption,” but present understanding is insufficient to rule out this possibility. The most promising avenue for increasing understanding of CO2 leakage behavior is the study of natural analogues.  相似文献   

15.
Freshwater marshes could be a source of greenhouse gases emission because they contain large amounts of soil carbon and nitrogen. These emissions are strongly influenced by exogenous nitrogen. We investigate the effects of exogenous nitrogen on ecosystem respiration (CO2), CH4 and N2O emissions from freshwater marshes in situ in the Sanjiang Plain Northeast of China during the growing seasons of 2004 and 2005, using a field fertilizer experiment and the static opaque chamber/GC techniques. The results show that there were no significant differences in patterns of seasonal variations of CO2 and CH4 among the fertilizer and non-fertilizer treatments, but the seasonal patterns of N2O emission were significantly influenced by the exogenous nitrogen. Seasonal averages of the CO2 flux from non-fertilizer and fertilizer were 987.74 and 1,344.35 mg m −2 h −1, respectively, in 2004, and 898.59 and 2,154.17 mg m −2 h −1, respectively, in 2005. And the CH4 from the control and fertilizer treatments were 6.05 and 13.56 mg m −2 h −1 and 0.72 and 1.88 mg m −2 h −1, respectively, in 2004 and 2005. The difference of N2O flux between the fertilizer and non-fertilizer treatments is also significant either in 2004 and 2005. On the time scale of 20-, 100-, and 500-year periods, the integrated global warming potential (GWP) of CO2 + CH4 + N2O released during the two growing seasons for the treatment of fertilizer was 97, 94 and 89%, respectively, higher than that for the control, which suggested that the nitrogen fertilizer can enhance the GWP of the CH4 and N2O either in long time or short time scale.  相似文献   

16.
The low-temperature isobaric heat capacities (C p) of β- and γ-Mg2SiO4 were measured at the range of 1.8–304.7 K with a thermal relaxation method using the Physical Property Measurement System. The obtained standard entropies (S°298) of β- and γ-Mg2SiO4 are 86.4 ± 0.4 and 82.7 ± 0.5 J/mol K, respectively. Enthalpies of transitions among α-, β- and γ-Mg2SiO4 were measured by high-temperature drop-solution calorimetry with gas-bubbling technique. The enthalpies of the α−β and β−γ transitions at 298 K (ΔH°298) in Mg2SiO4 are 27.2 ± 3.6 and 12.9 ± 3.3 kJ/mol, respectively. Calculated α−β and β−γ transition boundaries were generally consistent with those determined by high-pressure experiments within the errors. Combining the measured ΔH°298 and ΔS°298 with selected data of in situ X-ray diffraction experiments at high pressure, the ΔH°298 and ΔS°298 of the α−β and β−γ transitions were optimized. Calculation using the optimized data tightly constrained the α−β and β−γ transition boundaries in the P, T space. The slope of α−β transition boundary is 3.1 MPa/K at 13.4 GPa and 1,400 K, and that of β−γ boundary 5.2 MPa/K at 18.7 GPa and 1,600 K. The post-spinel transition boundary of γ-Mg2SiO4 to MgSiO3 perovskite plus MgO was also calculated, using the optimized data on γ-Mg2SiO4 and available enthalpy and entropy data on MgSiO3 perovskite and MgO. The calculated post-spinel boundary with a Clapeyron slope of −2.6 ± 0.2 MPa/K is located at pressure consistent with the 660 km discontinuity, considering the error of the thermodynamic data.  相似文献   

17.
Summary A new occurrence of monazite from Alinci, SE Yugoslavia, is described. Crystal morphology studies showed that crystals possess a platelike habit on T01 which we regard as a hitherto unknown morphological feature of monazite. The material has been analysed for uranium, thorium and rare earth element content using gamma spectrometry and inductively coupled argon-plasma atomic emission spectrometry (ICPAES). The monazite displays a complex chemical composition, essentially given as (REE+Y,Th,U,Fe)1.001P0.988O4. The infrared absorption spectra and X-ray diffraction data are in agreement with those for terrestrial monazite, although they indicate minor structural variations caused by the REE distribution in the Alinci monazite.
Monazit aus hydrothermalen Gängen von Alinci, Jugoslawien
Zusammenfassung Es wird ein neues Monazitvorkommen von Alinci, Jugoslawien, beschrieben. Kristallmorphologische Studien zeigten, daß die Kristalle einen plattigen Habitus nach (T01) aufweisen, eine nach Wissen der Autoren bisher unbekannte morphologische Erscheinung bei Monazit. Das Material wurde auf die Uran-, Thorium- und Seltenerdgehalte mit Gamma-Spektrometrie und induktiv gekoppelter Argonplasma-Atomabsorptions-Spektrometrie (ICPAES) analysiert. Der Monazit zeigt eine komplexe chemische Zusammensetzung, die im wesentlichen als (REE+Y,Th,U,Fe)1.001P0.988O4 angegeben werden kann. Die Ultrarotspektren und die Röntgenbeugungs-Daten stimmen mit jenen von terrestrischem Monazit überein, obwohl sie kleine strukturelle Variationen anzeigen, die durch die REE-Verteilung im Monazit von Alinci verursacht sind.
  相似文献   

18.
The accessory minerals apatite and sphene are the main carriers of REE in alkaline rocks.Their chondrite-normalized REE patterns decline sharply to the right as those of the host rocks,In the patterns an obvious negative Eu anomaly and a positive Ce anomaly can be seen in apatite and sphene,respectively.Zircon from alkaline rocks is different in REE pattern,I,e,. a nearly symmetric“V“-shaped pattern with a maximum negative Eu anomaly.Compared with the equivalents from granites,apatite,sphene and zircon from alkaline rocks are all characterized by higher (La/Yb)N ratio and less Eu depletion,As to the relative contents of REE in minerals,apatite,sphene and zircon are enriched in LREE,MREE and HREE respectively,depending on their crystallochemical properties.  相似文献   

19.
 From heat capacities measured adiabatically at low temperatures, the standard entropies at 298.15 K of synthetic rutile (TiO2) and nepheline (NaAlSiO4) have been determined to be 50.0 ± 0.1 and 122.8 ± 0.3 J mol−1 K, respectively. These values agree with previous measurements and in particular confirm the higher entropy of nepheline with respect to that of the less dense NaAlSiO4 polymorph carnegieite. Received: 23 July 2001 / Accepted: 12 October 2001  相似文献   

20.
Paleoproterozoic carbonaceous shales in the Tim-Yastrebovskii ancient rift, which underwent zonal metamorphism at 350–550°C, contain REE mineralization of silicates (allanite, thorite, and Ce-P huttonite) fluorcarbonates (bastnaesite and synchysite), phosphates (monazite and xenotime), and REE-bearing apatite. The reason for the wide occurrence of bastnaesite and other REE minerals is relatively high REE concentrations in the sulfide-bearing carbonaceous shales, with these elements accumulated in the organic matter in the course of diagenesis. Reaction textures with REE-bearing chlorite, bastnaesite, and allanite suggest that REE-bearing chlorite and bastnaesite provided REE for the forming of higher temperature allanite and monazite. This is corroborated by the REE patterns of the monazite, allanite, and bastnaesite, which are almost identical and are characterized by the strong predominance of LREE. The replacements of REE minerals during metamorphism at 350–550°C took place via a number successive transitions: (1) Mnz → Aln, Chl REE → Bst, Chl REE → Aln, Bst → Aln and (2) Bst → Mnz and Ap LREE → Mnz. These replacements can be accounted for by prograde metamorphic reactions.  相似文献   

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