Trace Elements of Multi-stage Minerals and Titanite U-Pb Dating for the Gneisses from Liansan Island, Sulu UHPM Belt

Gneisses with anatectic characteristics from the Liansan island in the Sulu UHPM (ultra-high pressure metamorphic) belt were studied for petrography, titanite U-Pb dating and mineral geochemistry. Three origins of garnets are distinguished: metamorphic garnet, peritectic garnet and anatectic garnet, which are formed in the stages of peak metamorphism, retrograde anatexis and melt crystallization, respectively. The euhedral titanite has a high content of REE and high Th/U ratios, which is interpreted as indicating that it was newly-formed from an anatectic melt. The LA-ICP-MS titanite U-Pb dating yields 214–217 Ma ages for the titanite (melt) crystallization. The distribution of trace elements varies in response to the different host minerals at different stages. At the peak metamorphic stage, Y and HREE are mainly hosted by garnet, Ba and Rb by phengite, Sr, Nb, Ta, Pb, Th, U and LREE by allanite and Y, U and HREE by zircon. During partial melting, Y, Pb, Th, U and REE are released into the melt, which causes a dramatic decline of these element contents in the retrograde minerals. Finally, titanite absorbs most of the Nb, U, LREE and HREE from the melt. Therefore, the different stages of metamorphism have different mineral assemblages, which host different trace elements.     

REE Geochemistry of Moderate－and High－Sulfur Coals from North Shanxi,China

Contents of the rare-earth elements(REE) in two coal seams from North Shanxi Province,China,were determined using the instrumental neutron activation method.Based on the REE distribution tpatterns,and correlation analysis and cluster analysis,the main conclusions were drawn as follows.The REE contents are controlled mainly by the coal-forming environments,but might be affected by acidic solution Jeaching after peat sedimentation.The REE distribution patterns should be nearly the same in the sublayers of the same coal seam,and the occurrence of abnormal patterns might indicate the geological effect during post-sedimentation.The REE in coals are present mainly in the inorganic phase,and might be derived mainly from terrigenous detrital minerals.Some harmful elements,such as V,P,Mo,Cr,Cu,Mo,Th and Cd,might have cleaning potential during processing and dressing by washing because they are associated with REE.     

中国琼雷地区玻璃陨石成分的初步研究

The geographical distribution and physical properties of Qionglei tektites from South China are described in the present paper. 12 samples of Qionglei tektites have been determined for major and minor elements such as A1; Ba, Ce, Co, Cr, Cs, Eu, Fe, Gd, Hf, La, Mg,Na, O, Rb, Sb, Sc, Si, Sin, Ta, Tb, Th, U, Yb, etc. by NAA techniques. The family to which the tektites belong correlations between main oxides and SiO2, relative REE abundances, REE distribution patterns, Th/U ratios, and their bearing on the evolutionary history and genesis of Qionglei tektites are also discussed.     

Geochemical Behaviors of REE and Other Trace Elements during the Formation of Strata-bound Skarns and Related Deposits: A Case Study of the Dongguashan Cu (Au) Deposit, Anhui Province, China

REE and other trace elements in the altered marbles, massive skarns and ores, as well as garnet and quartz were determined in order to examine the behaviors of trace elements during hydrothermal alteration. It is demonstrated that the high-field-strength (HFS) elements Zr, Hf, Th and Nb were immobile while other trace elements were mobile during the formation of skarns and related deposits. REE and ore-forming elements such as Cu and Ag in hydrothermally-altered marbles and skarns were provided primarily by hydrothermal fluids. In the direction transverse of the strata, the more deeply the marbles were altered, the higher the total REE abundance and the larger the negative Eu anomalies would be. The chondrite-normalized REE patterns of skarns are similar to those of the marbles, but the former are distinguished by much higher REE contents and more remarkable negative Eu anomalies. Those patterns were apparently not inherited from the marble protolith, but were controlled by garnets, which were determine     

REE and Other Trace Element Chemistry of Oldhamite（CaS） in the Qingzhen Chondrite（EH3） and Their Genetic Implications

Instrumental neutron activation analysis(INAA) of 14 single oldhamite grains separated from the Qingzhen chondrite (EH3) for refractory(La,Ce,Sm ,Eu,Yb,Lu,Ca,Sc,Hf, and Th),volatile (Na,Cr,Zn,Se,Br,etc.)and siderophile elements (Fe,Ni,Co,Ir,Au ,and As) revealed that oldhamite is highly rich in refractory elements.The mineral serves as the principal carrier of REE and contains about 80% of the REEs in the Qingzhen enstatite chondrite .Furthermore, the large enrichment of LREE relative to HREE is noticed in oldhamite from the Qingzhen .In general, the oldhamite from metal-sulfide assemblages is richer in REE than that from the matrix,i.e.,the earlier the oldhamite grains condensed, the richer they are in REE. Meanwhile.oldhamite is also rich in vol-atile elements such as Se,Br, etc.In terms of the distribution of trace elements in oldhamitc from the Qingzhen ,the chondrite is srggested to have resulted from high-temperature condensation of solar nebula.     

Geochemical characteristics and petrogenesis of the Dashipo-Heishantuo batholith in Beijing and its geological significanceEI北大核心CSCD

The early Jurassic Dashipo-Heishantuo batholith in Beijing, which consists of the Dashipo hornblende-biotite syenite and Heishantuo granite, exposed in the western Yanshan orogenic belt, eastern North China Craton. The Dashipo syenite is magnesian potassic intermediate rock enriched in large ion lithophile elements such as Rb, Ba, Sr, Pb and LREE, and relatively depleted in high field strength elements such as Nb, Ta, U, Th, Zr, Hf as well as P and Ti, with εNd(t) values from -12.1 to -12.2 and ISr values of 0.70506-0.70464. The Heishantuo granite is magnesian peraluminous high K calc-alkaline, with an enrichment of large ion lithophile elements and radioactive elements such as Rb, Ba, Th, U and Pb, and a depletion of HREE and high field strength elements such as Nb, Ta, Zr and Hf as well as Sr, P and Ti, with εNd(t) values from -15.5 to -18.0 and ISr values of 0.70516-0.70593. The magma of the Dashipo syenite is produced by fractional crystallization of mantle-derived K-rich mafic magma under high pressure. The partial melting of the lower crust, which was heated and metasomatised by the mantle-derived magma, produced granitic magma that intruded into the unconsolidated Dashipo syenite to form the concentric batholith. The petrology and geochemistry of the Dashipo hornblende-biotite syenite indicate that the water weakening was important for the lithospheric destruction within the interior part of the North China Craton. Meanwhile, the partial melting related to the double-diffusion of energy and chemical composition between mantle-derived magma and crustal rocks was an important mechanism for the Mesozoic calc-alkaline felsic magmatism occurred in the interior of the North China Craton. ©, 2015, Science Press. All right reserved.     

Morphology, Chemistry and U-Pb Geochronology of Zircon Grains In Quartz Monzodiorite from the Sunzhuang Area, Fanshi County, Shanxi Province

The morphology, REE geochemistry and U-Pb geochronology of zircons from quartz monzodiorite in the Sunzhuang area, Fanshi County, Shanxi Province are presented in this study. The zircon crystals can be classified into four main types as: AB, L, S and P, and 24 subtypes such as AB4, AB5, L5, and S3. The maximum crystallization temperature of zircon was estimated as 850°C, with the minimum of 550°C. The peak temperatures of the zircon crystallization range from 650°C to 700°C. The abundances of Th and U in the zircon grains show large variation with the Th/U values 0.4. The Th and U values also show a positive correlation in most zircons. The REE abundance of zircon in the quartz monzodiorite ranges from 280.4 ppm to 2143 ppm with an average of 856.4 ppm. The chondrite normalized zircon REE patterns show two types, one is characterized by HREE enrichment and LREE depletion with positive Ce-anomaly and negative Eu-anomaly whereas the other is HREE enriched and LREE depleted with negative Eu-anomaly but without positive Ce-anomaly, and relatively flat patterns. The LA-ICP-MS U-Pb geochronology on the zircons yields a mean age of 133±0.87 Ma. Our data on zircon morphology, composition and U-Pb geochronology reveal that the parent magma of the quartz monzodiorite which was emplaced during late Yanshanian had a mixed crust-mantle source, with crustal components dominating. The magma is inferred to have been water rich and alkaline with initial high oxygen fugacity. Post-magmatic hydrothermal activity occurred under relatively reducing conditions which was conductive for gold precipitation in the Yixingzhai gold deposit.     

U and Th Contents and Th/U Ratios of Zircon in Felsic and Mafic Magmatic Rocks: Improved Zircon-Melt Distribution Coefficients

High-precision data on U and Th contents and Th/U ratios of zircon obtained using secondary ion mass spectrometry analysis have been collected from the literature. Zircon in the granitic rocks has median values of 350 ppm U, 140 ppm Th, and Th/U=0.52; the recommended zircon-melt partition coefficients are 81 for DU and 8.2 for DTh. In zircon from mafic and intermediate rocks, the median values are 270 ppm U, 170 ppm Th, and Th/U=0.81, and the recommended zircon-melt partition coefficients are 169 for DU and 59 for DTh. The U and Th contents and Th/U ratios of magmatic zircon are low when zircon crystallizes in equilibrium with the melt. Increasing magma temperature should promote higher Th contents relative to U contents, resulting in higher Th/U ratios for zircon in mafic to intermediate rocks than in granitic rocks. However, when zircon crystallizes in disequilibrium with the melt, U and Th are more easily able to enter the zircon lattice, and their contents and Th/U ratios depend mainly on the degree of disequilibrium. The behavior of U and Th in magmatic zircon can be used as a geochemical indicator to determine the origins and crystallization environments of magmatic zircon.     

Geochemistry of the trace elements and rare-earth elements at the boundary between Cambrian Series 2 and Series 3 at Jianshan, South China: Paleoenvironmental and stratigraphic implications

The Jianshan section in Jianhe County,Guizhou Province,is a very important auxiliary section to the candidate stratotype at the boundary between Cambrian Series 2 and Series 3.Twenty four samples collected from the Jianshan section of the Kaili Formation were analyzed for the concentrations of trace element and rare-earth elements(REEs) by inductively coupled plasma mass spectrometry.The trace element and REE geochemical characteristics of the Kaili Formation at the Jianshan section show that trace element composition and REE distribution patterns across the section are covariant.Notably,at 44 m above the base of the Kaili Formation,most trace element contents and REEs concentrations are lower than those values observed below 44 m.Above 44 m,an increasing trend in the concentration of both trace elements and REEs is observed.These geochemical data indicate important,but subtle,changes at the 44 m horizon.If this is,in fact,verified by work in progress,geochemical criteria can provide additional supports for defining the top surface of Cambrian Series 2,especially in sections where Oryctocephalus indicus is absent.Trace element ratios,specifically Ni/Co,V/Cr,V/(Ni+V) and Th/U as well as Ce and Eu anomalies indicate that the sedimentary environment of the Kaili Formation at the Jianshan section was oxidizing,that benthic redox conditions were less oxic,and may have been influenced by freshwater as compared to the Balang area.Moreover,the Eu anomalies observed in the Kaili Formation are similar to the negative Eu anomalies observed in post-Archean sedimentary rocks,and reveal fluctuations in oxygen content from the bottom to the top of the Kaili Formation.     

稀土元素在海水中的运移形式与沉淀条件的某些实验研究

In this paper, some experimental studies on the forms of existenee and conditions for transport and precipitation of rare earth elements (REE) in sea water have been dealt with. The results show that the ions of REE and carbonate radicles can be combined into quite stable and soluh|e complex in the medium of weak alkalinity. REE precipitation may result from the decomposition of the REE complex during the transformation of the solution from weak alkalinity to neutrality and to weak acidity and in the presence of REE preeipitating agents, such as P, Ba, Ca, and Mg.This is the reason why REE can concentrate in carbonate formations. Experimental results also show that REE will be precipitated .in the form of phosphate or fluocarhanate, if there exist the anions of [PO4]^3- and F^- in certain quantity in the solution. The experimental results arc consistent with the geologioal characteristics of some REE deposits.     

Geochemistry of rare earth elements in oceanic phillipsites

The behavior of rare earth elements (REE) was examined in oceanic phillipsites collected from four horizons of eupelagic clay in the Southern Basin of the Pacific. The REE concentrations were determined in the >50-μm-fraction phillipsite samples by the ICP-MS method. The composition of separate phillipsite accretions was studied using the electron microprobe and secondary ion mass-spectrometry. Rare earth elements in phillipsite-only samples are related to the admixture of ferrocalcium hydroxophosphates. The analysis of separate phillipsite accretions reveals low (<0.1–18.1 ppm) REE (III) concentrations. The Ce concentration varies between 2.7 and 140 ppm. The correlation analysis shows that REE (III) are present as an admixture of iron oxyhydroxides in separate phillipsite accretions. Based on the REE (III) concentration in iron oxyhydroxides, we can identify two generations of phillipsite accretions. Massive rounded accretions (phillipsite I) are depleted in REE, while pseudorhombic (phillipsite II) accretions are enriched in REE and marked by a positive Ce anomaly. Oceanic phillipsites do not accumulate REE or inherit the REE signature of the volcaniclastic material and oceanic deep water. Hence, the REE distribution in phillipsites does not depend on the sedimentation rate and host sediment composition.     

The role of carbonate-fluoride melt immiscibility in shallow REE deposit evolution

The Lugiin Gol nepheline syenite intrusion, Mongolia, hosts a range of carbonatite dikes mineralized in rare-earth elements(REE). Both carbonatites and nepheline syenite-fluorite-calcite veinlets are host to a previously unreported macroscale texture involving pseudo-graphic intergrowths of fluorite and calcite. The inclusions within calcite occur as either pure fluorite, with associated REE minerals within the surrounding calcite, or as mixed calcite-fluorite inclusions, with associated zirconosilicate minerals. Consideration of the nature of the texture, and the proportions of fluorite and calcite present(～29 and 71 mol%,respectively), indicates that these textures most likely formed either through the immiscible separation of carbonate and fluoride melts, or from cotectic crystallization of a carbonatefluoride melt. Laser ablation ICP-MS analyses show the pure fluorite inclusions to be depleted in REE relative to the calcite. A model is proposed, in which a carbonate-fluoride melt phase enriched in Zr and the REE, separated from a phonolitic melt, and then either unmixed or underwent cotectic crystallization to generate an REE-rich carbonate melt and an REE-poor fluoride phase. The separation of the fluoride phase(either solid or melt) may have contributed to the enrichment of the carbonate melt in REE, and ultimately its saturation with REE minerals. Previous data have suggested that carbonate melts separated from silicate melts are relatively depleted in the REE, and thus melt immiscibility cannot result in the formation of REE-enriched carbonatites. The observations presented here provide a mechanism by which this could occur, as under either model the textures imply initial separation of a mixed carbonate-fluoride melt from a silicate magma. The separation of an REEenriched carbonate-fluoride melt from phonolitic magma is a hitherto unrecognized mechanism for REE-enrichment in carbonatites, and may play an important role in the formation of shallow magmatic REE deposits.     

Geochemical behavior of rare-earth elements and other major and minor elements in soundproducing and silent beach sands in Japan

The major element composition of sound-producing sand is reported together with rare-earth elements (REE) and other selected elements for the first time. Rare-earth element concentrations in beach sands from Miyagi and Tottori in Japan were determined by induction-coupled, argon-plasma spectrometry (ICP-MS) to characterize the REE of sound-producing and silent sands relative to the parental rocks. Sound-producing sand beaches are very common and all over in Japan: five beaches in Miyagi and 2 in Tottori are selected with other silent sand beaches in the areas. Both sound-producing sand and silent sand samples from Miyagi and Tottori contain more than 60wt% of SiO2 and are composed mainly of quartz and feldspar. Miyagi sand samples are characterized by light REE enrichment and flat chondrite-normalized patterns that are similar to those of local source sandstone. However, all sand samples from Miyatojima in Miyagi show positive Eu anomalies, a characteristic feature not shown in other sand samples from Miyagi. Tottori sand samples also are characterized by high REE contents and remarkable positive Eu anomalies. The sands containing lower REE contents are due to high quartz and feldspar contents. Miyatojima sand samples and Tottori sand samples have high REE contents and show remarkable positive Eu anomalies due to the presence of feldspar. The best results are obtained using all of the geological methods and the Principal Component Analysis (PCA) as a measure of the similarity between sound-producing sand and silent sand. The difference between sound-producing sand and silent sand is obtained from the PCA results.     

Behaviours of REE and Other Trace Elements During Pedological Weathering-Evidence from Chemical Leaching of Loess and Palaeosol from the Luochuan Section in Central China

The chemical leaching method is used for a systematic analysis of distribution characteristics of acid-soluble and acid-insoluble REE and other trace elements from the Luochuan loess deposits. The study shows that the acid-insoluble phase in loess and palaeosol is a stable component of old aeolian dusts and is characteristic of the provenance; the acid-soluble phase is the unstable component in the weathering pedogenic process and reflects rock-forming features after accumulation of aeolian dusts. The acid-insoluble REE and acid-soluble Sr and Pb can be used as geochemical indicators respectively to trace the provenance characteristics and the weathering pedogenic process.     

Compositional Characteristics of Wolframite in Tin Dposits,Dupangling,Guangxi

Statistical data on major,trace and rare-earth elements in wolframite from the quartz vein-and greisen-type tin deposits in the Dupangling orefield reveal(1)The components in wolframite can be divided into two relatively independent groups:the WO3-Nb-Ta-Sc-REE group,in which WO3 is negatively correlated with the others and the FeO-MnO-Sn group,in which MnO is negatively corre-lated with the other two;(2)In general ,REE fractionation is not significant,reflected mainly by the separation of Eu from other REE‘s.LREE and HREE increase or decrease simultaneously ,with HREE being more variable;(3)Nb,Ta,Sc,REE substitute for W, and Sn may enter into wolframite lattice accompanied by Fe-Mn substitution;(4)In contrast to wolframite in quartz veins,which is poor in REE,Nb,Ta and has high δEu values and LREE/HREE and Nb/Ta ratios,wolframite in greisen is rich in REE, Nb,Ta,Sc and has low δEu values and LREE/HREE and Nb/Ta ratios ;and (5)The contents and ratios of trace elements and REE parti-tioning parameters of wolframite can be used as guide for prospecting.     

Trace element and REE geochemistry of the Zhewang gold deposit,southeastern Guizhou Province,China

The quartz vein-type gold deposits are widely hosted by the Neoproterozoic （Xiajiang Group） epimeta- morphic clastic rock series in southeastern Guizhou Province, China. The Zhewang gold deposit studied in this paper occurs in the second lithologieal member of the Pinglue Formation of the Xiajiang Group. Trace element geochemis- try of host rocks, quartz veins and arsenopyrite has revealed that ore-forming fluid was enriched in sulphophile ele- ments such as Au, Ag, As, Sb, Pb and Zn, and simultaneously concentrated some magmaphile elements such as W and Mo, which probably provides some evidence for multi-stage mineralization or overprinting of magmatic hydro- therm. Quartz veins and arsenopyrite were characterized by depletion in HFSE and enrichment in LREE. Hf/Sm, Nb/La and Th/La imply that the ore-forming fluid was probably a NaC1-H20 solution system enriched in more C1 than F; Th/U values reflect the strong reducibility of the ore-forming fluid, coincident with the sulfide assemblages. The values of Co/Ni reflect that magmatic fluids may have partly participated in the ore-forming process and Y/Ho values have proved that the ore-forming fluid was associated with metamorphism and exotic hydrotherm which has reformed former quartz veins during late mineralization. The concentrations of REE, Eu anomalies and Ce anomalies of this deposit display that ore-forming elements mainly were derived from host rocks and possibly from a mixed deep source, and the ore-forming fluid was mixed by dominant metamorphic fluid and minor other sources. The physical-chemical conditions of ore-forming fluid changed from the initial stage to the late stage. The metamorphic fluid is responsible for the mineralization. Therefore, the Zhewang gold deposit is classified as a quartz vein-type gold deposit which may have been reformed by magmatic fluids during the late stage.     

Geochemical characteristics of the coal gangues from the Du’erping coal mine,Xishan coalfield,North China

Inductively coupled plasma mass spectrometry, inductively coupled plasma optical emission spectroscopy, hydride generation-atomic fluorescence spectrometry, emission spectrometry, X fluorescence spectrometry, and X-ray diffraction were employed to study the geochemistry and mineralogy of coal gangues from Nos. 2, 3, and 8 coal seams of the Du’erping coal mine, Xishan coalfield, Taiyuan, Shanxi Province. The study revealed that compared with the sedimentary cover, upper continent crust, Carboniferous-Permian coal from North China, as well as most coal in China, coal gangues from Nos. 2 and 3 coal seams are rich in Li, Be, Sc, Cr, Cu, Ga, Ba, Th, Nb, Cd, Pb, Ta and rare-earth elements, and coal gangues from No. 8 coal seam are rich in Li, Sc, V, Cr, Ga, U, and rare-earth elements. Compared with the Carboniferous-Permian coal from North China and most coal in China, coal gangues from Nos. 2, 3 and 8 seams are rich in Rb, V, Cs and Sr. Therefore, The Du’erping coal gangues in the Xishan coalfield are rich in most hazardous trace elements and rare-earth elements, wherein the contents of Ga and Li reach the industrial grade and have significance for industrial utilization. On the whole, coal gangues of the Shanxi Formation from the Permian are rich in more trace elements than those of the Carboniferous Taiyuan Formation. The distributions of REE show obviously dipping rightwards with negative Eu anomalies. The contents of rare-earth elements in the three seams are quite different. All of the above indicate that the source of the rare-earth elements is terrigenous debris. Minerals in No. 2 seam identified by X-ray diffraction mainly include quartz, kaolinite, in addition to calcite, pyrite, apatite, epidote, and epsomite. No. 3 seam mainly contains quartz, kaolinite, in addition to a small amount of sodium feldspar, calcium nitrate, iron ore, gypsum, and vivianite. No. 8 seam mainly contains kaolinite, dickite, quartz, illite, and a small amount of hematite and U. The correlations between major elements and trace elements in coal gangues of the Du’erping coal mine analyzed by using SPSS (Statistical Product and Service Solutions) indicate that the trace alkali elements and rare-earth elements occur mainly in such clay minerals as kaolinite.     

Mineralogy,M-type tetrad effect and radioactivity of altered granites at the G. Abu Garadi shear zone,central Eastern Desert,Egypt

The G. Abu Garadi area is covered mainly by metasediments, alkali feldspar granites and stream sediments. The alkali feldspar granite is traversed by a major strike-slip fault trending in an N-S direction as well as two subordinate sets of faults trending NW to WNW for the first one and NE for the second one. These faults represent the shear zones affected by magmatic (syngenetic) as well as hydrothermal (epigenetic) activities causing alteration of the granitic rocks. The most common alteration features are albitization, greisenization and koalinitization. The mass balance calculations of the studied altered samples show enrichments in Zr, Y, Ni, U, Th and Ga and depletions in Zn, Sr, Nb, Ba, Pb, Cu and V. Only the greisenized samples exhibit a significant enrichment in Nb, ∑REE budget and pronounced lanthanide tetrad effect (M-type), especially TE1,4, while weakly expressed tetrad effects are for the other albitized and koalinitized samples. Mineralogically, the common accessory minerals in the altered samples include samarskite-(Y), betafite, uranothorite, zircon, fluorite and cassiterite. The greisenized granites contain high eU and eTh than the other altered types, where they are characterized by an assemblage of the radioactive minerals; samarskite-(Y), betafite, uranothorite in addition to zircon. The inter-element relationships between U and Th and also their ratios illustrate that the radioelement distribution in these granites is mainly governed by magmatic processes, in addition to post-magmatic ones. The distribution of chemical elements and the fractionation of some isovalents within the shear zone are largely controlled by the newly formed mineral phases. With respect to uranium mobilization, uranium migrated from the host alkali feldspar granites of G. Abu Garadi, while the shear zones acted as traps for the migrated uranium. Moreover, U migrated in the shear zone during greisenization and albitization, and migrated out during koalinitization.     

Concentrations and distribution of elements in milled-coal, power plant ashes and stack-emitted materials in a Western Canadian coal-fired power plant

The focus of this study is to determine the concentrations and the distributions of elements of prime environmental concern （As, Cd, Cr, Cu Hg, Mo, Ni, Pb, Se and V） and other elements of environmental interest （B, Ba, Be, Co, Mn, U） in milled coals, power plant ashes, and stack-emitted materials from a Western Canadian power plant using bituminous coal. The concentrations of elements were determined using neutron activation analysis （NAA）, Inductively Coupled Plasma Emission Spectroscopy （ICPES）, and Inductively Coupled Plasma-Mass spectroscopy （ICP-MS） for most elements, Graphite Furnace Atomic Absorption （GFAA） for Pb, and Cold Vapor Atomic Absorption （CVAA） for Hg. The result of the study shows that the total rate of input is 423.5 kg/d for elements of prime environmental concern and 280 kg/d for elements of environmental interest. The concentrations of most elements in milled coal are low as compared to world coals and other Canadian milled coals. The total output of these two groups of elements is 2.9 kg/d and 110.4 kg/d, respectively. This indicates that only a small amount of the total input elements from the milled coal is emitted. Most of it is captured by the bottom and ESP ashes with the exception of the highly volatile As Hg, F, Br, and Cl. The element with highest rate of emission for elements of prime environmental concern is Se （0.73 kg/d） and B （95 kg/d） for the elements of some environmental interest.     

Newly developed evidence for the original Tethysan island-arc volcanic rocks in the southern segment of the South Lancangjiang Belt

This paper re-describes the characteristics of pre-Ordovician (Pt3) metamorphic volcanic rocks in the Huimin-Manlai region of Yunnan Province from the aspects of petrographic characteristics, rock assemblage, petrochemistry, REE, trace elements, lead isotopes and geotectonic setting. The metamorphic volcanic rocks maintain blasto-intergranular and blasto-andesitic textures; the volcanic rocks are characterized by a basalt-andesite-dacite assemblage; the volcanic rocks are basic-intermediate-intermediate-acid in chemical composition, belonging to semi-alkaline rocks, with calc-alkaline series and tholeiite series coexisting, and they are characterized by low TiO2 contents; their REE distribution patterns are of the LREE-enrichment right-inclined type; the volcanic rocks are enriched in large cation elements and commonly enriched in Th and partly depleted in Ti, Cr and P, belonging to the Gondwana type as viewed from their Pb isotopic composition; petrochemically the data points fall mostly within the field of island-arc volcanic rocks. All these characteristics provided new evidence for the existence of original Tethysan island-arc volcanic rocks in the region studied.