“寨背式”离子吸附型稀土矿床多类型稀土矿化及其成因

赣南寨背离子吸附型稀土矿床产于寨背复式花岗岩体的风化壳中,自20世纪80年代发现以来一直以轻稀土型开采,近年在轻稀土型花岗岩风化壳中发现了重稀土矿。为了探讨轻稀土型花岗岩风化过程中重稀土元素的迁移、分馏和富集机制,本文选择了区内三个具有代表性的风化壳钻孔(ZK1、ZK2和ZK4)对其进行了全相和离子交换相稀土元素地球化学研究。结果显示：钻孔ZK4中离子交换相稀土含量介于14.90×10^-6～835.8×10^-6之间,并富集轻稀土(LREE/HREE=2.28～10.78);钻孔ZK1中离子交换相稀土含量达1470×10^-6(9件样品均值),具有从轻稀土型向重稀土型过渡的配分特征(LREE/HREE=1.30～1.65),并且剖面自上而下显示轻、重稀土逐渐富集的趋势;钻孔ZK2中离子交换相稀土含量为492.4×10^-6(8件样品均值),自上而下稀土配分类型从轻稀土型过渡至重稀土型(LREE/HREE=0.43～2.25),且轻稀土富集在全风化层上部而重稀土则富集在下部。三个钻孔的Nb/Ta和Zr/Hf...     

Petrogenesis and Dating of Two Types of Granite from North Qilian, China

1 IntroductionThree E-W-trending lithologic belts of the Paleozoic ageoccur in the eastern part of north Qilian. From north tosouth they are (a) the Huangyanghe-Gulang-Dajing-Beidengzi belt (the northern lithologic belt), (b) theLeigongshan-Maomaoshan-Laohushan belt (the middlelithologic belt) and (c) the Mayaxieshan-Shihuigou-Beiyinbelt (the southern lithologic belt) (Fig. 1). The rocks inthese belts are mainly Paleozoic volcanics and sandysiltstone. There are some Mesozoic and Cenozo…     

Rare earth element fractionation in authigenic illite–smectite from Late Permian clastic rocks,Bowen Basin,Australia: implications for physico-chemical environments of fluids during illitization

REE analyses were performed on authigenic illitic clay minerals from Late Permian mudrocks, sandstones and bentonites from the Bowen Basin (Australia). The mixed-layer illite–smectite exhibit REE patterns with an obvious fractionation of the HREE from the LREE and MREE, which is an apparent function of degree of illitization reaction. The highly illitic (R≥3) illite–smectite from the northern Bowen Basin show a depletion of LREE relative to the less illitic (R=0 and 1) clays. In contrast, an enrichment of HREE for the illite-rich clays relative to less illitic clays is evident for the southern Bowen Basin samples. The North American Shale Composite-normalized (La/Lu)_sn ratios show negative correlations with the illite content in illite–smectite and positive correlations with the δ¹⁸O values of the clays for both the northern and southern Bowen Basin samples. These correlations indicate that the increasing depletion of LREE in hydrothermal fluids is a function of increasing water/rock ratios in the northern Bowen Basin. Good negative correlations between (La/Lu)_sn ratios and illite content in illite–smectite from the southern Bowen Basin suggest the involvement of fluids with higher alkalinity and higher pH in low water/rock ratio conditions. Increasing HREE enrichment with δ¹⁸O decrease indicates the effect of increasing temperature at low water/rock ratios in the southern Bowen Basin.Results of the present study confirm the conclusions of some earlier studies suggesting that REE in illitic clay minerals are mobile and fractionated during illitization and that this fact should be considered in studies of sedimentary processes and in identifying provenance. Moreover, our results show that REE systematic of illitic clay minerals can be applied as an useful technique to gain information about physico-chemical conditions during thermal and fluid flow events in certain sedimentary basins.     

浙江八面山萤石矿床稀土元素地球化学特征及成因探讨

对浙江八面山萤石矿床中不同类型萤石矿石和围岩样品的稀土元素的系统分析表明,细粒萤石矿石的ΣREE〈39×10-6,LREE为14.36×10-6～34.24×10-6,HREE0.96×10-6～2.04×10-6,Y〈3×10-6;巨晶萤石矿石中的ΣREE3.62×10-6～20.81×10-6,LREE2.71×10-6～17.67×10-6,HREE0.24×10-6～1.49×10-6;而围岩花岗岩的ΣREE460.29×10-6,LREE225.97×10-6,HREE91.32×10-6,Y＆gt;140×10-6;沉积岩中的ΣREE20.22×10-6、LREE16.11×10-6、HREE1.61×10-6。矿石与围岩中沉积岩的稀土总量、轻稀土、重稀土和Y的含量接近,与花岗岩的稀土总量、轻稀土、重稀土和Y元素含量相差悬殊。萤石矿石的稀土分布型式主要为轻稀土富集型,（La/Yb）N通常多数大于8,在8.07～17.26间,δEu值在0.45～1.30,δCe在0.89～1.14间,Ce、Eu基本不显异常。矿石与围岩的稀土地球化学研究显示,八面山萤石矿床为受地层、岩体与断裂共同控制＂三位一体＂的低温热液型矿床。     

邹家山铀矿床伴生重稀土元素的赋存特征

初步研究发现,相山矿田邹家山矿床中伴生有较高的重稀土元素,回收这些珍稀的资源和探索其成因具有重要的意义,而查明这些伴生稀土在铀矿床中的赋存特征是前期基础性工作。为此本文采用电子探针和激光剥蚀电感耦合等离子体质谱分析了邹家山铀矿床中稀土元素的赋存状态。结果显示：该矿床稀土矿物主要为独居石、氟碳钙铈矿和磷钇矿;独居石、氟碳钙铈矿的LREE/HREE>1,为轻稀土富集型;而磷钇矿的LREE/HREE<1,为重稀土富集型。沥青铀矿、钛铀矿、铀钍石、铀石、钍石、锆石等铀钍矿物的稀土特征为重稀土富集型;铀钍矿物稀土总量（∑REE+Y）较高,为（3 805.78~65 307.00）×10^-6,LREE/HREE<1,为0.01~0.80,平均为0.29。其他伴生矿物磷灰石、钾长石为轻稀土富集型,萤石为轻、重稀土富集型两类都有,而伊利石、黄铁矿的轻重稀土无明显相对富集。重稀土在磷钇矿和铀钍矿物中以类质同象形式存在,少量赋存于伴生矿物。     

潘集煤矿二叠纪主采煤层中微量元素亲和性研究

安徽淮南煤田位于华北地台南端 ,发育了华北地区二叠纪含煤岩系中层位最高的可采煤层。采用仪器中子活化分析法 (INAA)测试了淮南煤田潘集煤矿二叠纪主采煤层 13个样品的 36个微量元素的浓度分布 ,并对其共生组合特点、地球化学特征及稀土元素配比模式作了初步分析 ,结果表明 ,煤中不同微量元素显示出不同的亲和性质。元素Br,As ,Sb ,Ni和Co等趋于在煤中富集 ,其中Br的有机亲和性最大。元素Na ,K ,Rb ,Th ,Hf,Zr ,Ta和REE则在煤层与顶底板接触带的碳质泥岩中富集 ,表现出与细粒陆源碎屑物更强的亲和性。其它元素倾向性不甚明显 ,但Fe ,Ca ,Sr ,HREE等元素在海水影响强度增大的煤层中含量增加。元素As,Cs,Ni,Fe和Ca在煤层中含量变化较大 ,其变异系数大于 1,其它元素则相对稳定 ,表明同一矿区煤层中微量元素含量在不受其它地质作用明显叠加影响时具有一定的稳定性。本区煤层稀土元素配比模式与华北其它地区C—P纪煤基本类似 ,普遍存在Eu亏损现象。 ∑REE在煤中分布范围为30× 10 -6～ 95× 10 -6,在顶板泥岩中超过 2 0 0× 10 -6。煤层中部 ∑REE降低 ,HREE相对富集。聚类分析表明 ,元素As ,Se ,Ag和Fe关系密切 ,这与煤中黄铁矿等成岩矿物有直接关系 ,泥炭沼泽演化期间或之后海水的直接或间接影响会促使这     

内蒙古宝日拉锦乌拉钠闪石花岗岩特征

宝日拉锦乌拉钠闪石花岗岩岩体位于大兴安岭中段东坡,形成于早白垩世晚期或更晚些.钠闪石花岗岩富SiO₂（含量为71.63%~77.35%）,富碱（ALK=4.94%~9.17%）,贫铝、镁、钙.钠闪石花岗岩的稀土元素总量极高,其中钠闪石钾长花岗岩的稀土总量在271.77×10^-6~701.77×10^-6之间,而钠闪石二长花岗岩中的稀土元素总量在2938×10^-6~6933.2×10^-6之间.轻、重稀土元素比值在1.63~7.49之间,大部分在2~5之间,稀土配分曲线为略呈右倾的“V”字形,说明轻、重稀土元素的分馏程度较差.δEu值极低,在0.016~0.035之间,说明该岩石的Eu负异常极为明显.研究区出露的钠闪石花岗岩形成于板块内部非造山的相对稳定的构造环境.     

REE Geochemistry and Mineralization Characteristics of the Zudong and Guanxi Granites,Jiangxi Province

Abstract The Zudong and Guanxi granites are original rocks of the ion adsorption-type HREE and LREE deposits in weathering crust of granites. The ∑REE ¹ ∑REE=REE+Y.
value and LREE ² LREE=∑(La-Eu) and HREE=∑(Gd-Lu)+Y.
/ HREE ratio of the Zudong granite are 264 ppm and 0.81-0.24 respectively, and the average Y/∑REE ratio is 35.8-54.5%. This is mainly due to magmatic crystallization and evolution and deuteric metasomatism (albitization, muscovitization and fluorite-doveritization). These alterations resulted in endogenic mineralizations of yttrium-group REE fluorine carbonates, silicates and arsenates. The Guanxi granite is characterized by LREE enrichment (the average LREE/HREE ratio is 2.43).     

湘江悬浮物的稀土元素地球化学研究

在湘江及其支流采集了44件悬浮物样品进行稀土元素 ICP—MS分析。研究表明,湘江悬浮物中稀土总量(∑REE)、轻稀土(LREE) 和重稀土(HREE)含量分别为63～387 μg/g,58.2～353 μg/g和4.8～34μg/g。尽管湘江悬浮物中稀土分布不均匀,稀土含量相差很大,所有样品的球粒陨石标准化曲线均呈向右倾斜的富LREE的模式,北美页岩标准化模式为LREE稍富集的平坦型。湘江中下游河心与两岸水体悬浮物中稀土发生了明显分异。湘江悬浮颗粒物中REE受多方面因素控制,其源区控制了REE分配模式,而其稀土元素含量与颗粒中粘土矿物及重矿物有关。支流捞刀河悬浮物稀土的分布模式为Eu正异常型,与北美页岩有显著差别,捞刀河的悬浮物物源及成因有待进一步研究。     

浙东南松阳县枫坪组沉积岩碎屑锆石年代学及地质意义

利用激光剥蚀电感耦合等离子质谱技术(LA-ICP-MS)对浙东南松阳县枫坪组地层底部的细砂岩进行了锆石U-Pb定年及稀土元素分析。样品中大部分碎屑锆石具有较好的振荡环带且Th/U值大于0. 1,表明其为岩浆成因。碎屑锆石中稀土元素含量变化范围较大,(La/Yb)_N值为0～0. 29,LREE/HREE值为0. 003×10~(-6)～0. 977×10~(-6),表明样品中锆石的轻、重稀土元素分异程度较小且重稀土元素相对富集,具有轻稀土元素含量低、重稀土元素含量高的左倾模式且具有负Eu异常、正Ce异常的特征,表明碎屑锆石主要以岩浆锆石为主,同时存在少量的变质锆石。碎屑锆石U-Pb测年结果表明,最年轻的锆石年龄为193 Ma,显示枫坪组沉积岩成岩年龄不晚于193 Ma。碎屑锆石年龄可分为4组,分别为2 461～1 743 Ma、887 Ma、435和422 Ma、330～193 Ma。碎屑锆石的主要年龄区间分别与已知的构造-岩浆热事件时间相对应(吕梁期、晋宁期、加里东期和印支-海西期),表明本区的构造岩浆活动与中国大地构造运动相一致,并具有幕式发展的特征。通过对枫坪组沉积岩碎屑锆石U-Pb年龄的系统分析并与可能物源区的年代学对比研究,认为枫坪组沉积岩物质来源主要是周边出露的中条期侵入岩体和浙东南出露的印支期花岗岩体。     

1.5GPa、950℃下块状斜长角闪岩部分熔融微量元素的分配特征

在1.5GPa,950℃,恒温101h条件下对华北北缘太古宙地体中的斜长角闪岩块状样品进行了脱水部分熔融实验,实验产物组合为Hb+Cpx+Gt+Gl,获得的熔体为花岗闪长质成分。利用LA-ICP-MS测试了矿物和熔体的微量元素,获得该体系内各矿物/熔体的微量元素分配系数。角闪石、单斜辉石和石榴石的分配系数与前人在类似条件下的实验结果基本一致。这说明无论实验的初始物质是粉末状还是块状,对元素的分配没有太大的影响。各矿物的REE分配系数对离子半径的拟合曲线很好地符合晶格应变弹性模型。整体特征上,角闪石、单斜辉石和石榴石的LILE,LREE分配系数较低,而HREE的分配系数较高,石榴石具有强烈富集HREE的特征。由此,造成实验熔体表现出LILE、LREE富集而HREE亏损的特征。残留相中无金红石,使得熔体中没有明显的Nb、Ta负异常。熔体的主-微量元素特征符合华北北缘中生代埃达克质岩石的基本特征,进一步支持了该类岩石"可能起源于古老下地壳的部分熔融"的成因模式。     

江西足洞和关西花岗岩的稀土元素地球化学及矿化特征

足洞和关西岩体分别为花岗岩风化壳离子吸附型重、轻稀土矿床的原岩。足洞岩体的∑REE¹⁾为264ppm,LREE/HREE²⁾值为0.81-024,平均的钇对∑REE占有率为35.8-54.5%。这主要是由于岩浆结晶演化及晚期有交代钠长石化、白云母化和萤石-氟碳钙钇矿化的结果。这些蚀变产生了钇族稀土氟碳酸盐、硅酸盐和砷酸盐等内生矿化作用。     

Behaviour of REE and mass balance calculations in a lateritic profile over chlorite schists in South Cameroon

An in situ weathering profile overlying chlorite schists in the Mbalmayo-Bengbis formations (South Cameroon) was chosen for the study of the behaviour of REE and the evaluation of geochemical mass balance. After physical and mineralogical studies, the chlorite schists and the undisturbed weathered materials were chemically analyzed for major elements (X-ray fluorescence and titrimetry) and REE (ICP-MS). The behaviour of the REE in the Mbalmayo weathering system was established in comparison with the REE of the reference parent rock. Mass balance calculations were applied to both major elements and REE. The mineralogy of the materials was determined with the aid of a Philips 1720, diffractometer. The chlorite schists of the Mbalmayo sector show low REE contents (Σ=153.44 ppm). These rocks are relatively rich in LREE (about 125 times the chondritic value) and relatively poor in HREE (about 20 times the chondritic value). The REE diagram normalized to chondrites shows a slightly split graph ((La/Yb)_N=6.18) with marked enrichment in LREE (LREE/HREE=9.50) in relation to HREE. Moreover, these spectra do not present any Ce anomaly, but a slightly positive Eu anomaly. The imperfectly evolved profile, whose materials are genetically linked, shows an atypical behaviour of REE. In effect, the LREE are more mobile than the HREE during weathering ((La/Yb)NASC<1) with weak Ce anomalies. This has been rarely reported in lateritic profiles characterized by higher HREE mobility than LREE during weathering processes with high Ce anomalies. This is either due to the difference in the stability of REE-bearing minerals, or to the weak acidic to basic pH conditions (6.70<pH<7.80), or even due to the average evolution of the weathering materials. The pathway of the REE along the profile is as follows: (1) leaching in the saprolites and summit of the profile, except for Ce, which precipitates very weakly in the nodular materials and the coarse saprolite materials, (2) at the base of the profile, solutions come in contact with chlorite schist formations, at this level, the pH increases (pH=7.79), HREE and a part of LREE partially void of Ce precipitate and (3) the other part of LREE precipitates further up in the profile. The geochemical mass balance calculations reveal that these elements are leached in the same phases as the relatively high Si, Al, K and Fe²⁺ contents.     

Major Element Compositions and Rare—earth Element Abundaces of Cenozoic Basalts in Eastern China：Implications for a Pressure Control over LREE／HREE Fractionation in Continental Basalt

Major element compositions and rare-earth element (REE) and transition element(Ni,Cr and V) abundances have been determined on 44 basalt samples from eastern China.These basalts have SiO2 contents ranging from 38.63 to 55.24(wt.%),and Na2O K2O from 3.1 to 9.4(wt.%).Ni and Cr abundances are largely variable,respectively falling in ranges 60-605 and 78-1150 ppm.REE abundances,especially light rare-earth elements(LREE), are highly variable.La/Sm and La/Yb ratios vary 2.8 to 7.6 and 1.8 to 8.1. Although the segregation mainly of olivine and clinopyroxene is requested to account for the vari-able and low MgO,CaO/Al2O3,Cr and Ni characteristic of these basalts studied here,the differ-ences in REE composition of the basalts are still related mainly to the partial melting process.Obvious varations in REE abundances could be principally attributed to the partial melting process.Obvious variations in REE abundances could be principally attributed to the partial melting processes that took place at different depths,in spite of some variations caused by the fractional crystallization processes.REE abundances and La/Sm and La/Yb ratios systematically decrease with increasing SiO2,which probably indicated that the basaltic magma derived from a deeper level has higher LREE and LREE/HREE ratios than that from a shallower level.As viewed from the fact that the D^Yb/D^La ratios of clinopyroxenes in the basaltic system increase with increasing pressure,the increase of LREE/HUEE ratios with increasing melting depth can be interpreted as the pressure dependence of bulk D^HREE/D^LREE ratios of silicate minerals,in addition to the pressure control over the melting degree.     

Rare Earth Deposits of North America

Rare earth elements (REE) have been mined in North America since 1885, when placer monazite was produced in the southeast USA. Since the 1960s, however, most North American REE have come from a carbonatite deposit at Mountain Pass, California, and most of the world’s REE came from this source between 1965 and 1995. After 1998, Mountain Pass REE sales declined substantially due to competition from China and to environmental constraints. REE are presently not mined at Mountain Pass, and shipments were made from stockpiles in recent years. Chevron Mining, however, restarted extraction of selected REE at Mountain Pass in 2007. In 1987, Mountain Pass reserves were calculated at 29 Mt of ore with 8.9% rare earth oxide based on a 5% cut‐off grade. Current reserves are in excess of 20 Mt at similar grade. The ore mineral is bastnasite, and the ore has high light REE/heavy REE (LREE/HREE). The carbonatite is a moderately dipping, tabular 1.4‐Ga intrusive body associated with ultrapotassic alkaline plutons of similar age. The chemistry and ultrapotassic alkaline association of the Mountain Pass deposit suggest a different source than that of most other carbonatites. Elsewhere in the western USA, carbonatites have been proposed as possible REE sources. Large but low‐grade LREE resources are in carbonatite in Colorado and Wyoming. Carbonatite complexes in Canada contain only minor REE resources. Other types of hard‐rock REE deposits in the USA include small iron‐REE deposits in Missouri and New York, and vein deposits in Idaho. Phosphorite and fluorite deposits in the USA also contain minor REE resources. The most recently discovered REE deposit in North America is the Hoidas Lake vein deposit, Saskatchewan, a small but incompletely evaluated resource. Neogene North American placer monazite resources, both marine and continental, are small or in environmentally sensitive areas, and thus unlikely to be mined. Paleoplacer deposits also contain minor resources. Possible future uranium mining of Precambrian conglomerates in the Elliott Lake–Blind River district, Canada, could yield by‐product HREE and Y. REE deposits occur in peralkaline syenitic and granitic rocks in several places in North America. These deposits are typically enriched in HREE, Y, and Zr. Some also have associated Be, Nb, and Ta. The largest such deposits are at Thor Lake and Strange Lake in Canada. A eudialyte syenite deposit at Pajarito Mountain in New Mexico is also probably large, but of lower grade. Similar deposits occur at Kipawa Lake and Lackner Lake in Canada. Future uses of some REE commodities are expected to increase, and growth is likely for REE in new technologies. World reserves, however, are probably sufficient to meet international demand for most REE commodities well into the 21st century. Recent experience shows that Chinese producers are capable of large amounts of REE production, keeping prices low. Most refined REE prices are now at approximately 50% of the 1980s price levels, but there has been recent upward price movement for some REE compounds following Chinese restriction of exports. Because of its grade, size, and relatively simple metallurgy, the Mountain Pass deposit remains North America’s best source of LREE. The future of REE production at Mountain Pass is mostly dependent on REE price levels and on domestic REE marketing potential. The development of new REE deposits in North America is unlikely in the near future. Undeveloped deposits with the most potential are probably large, low‐grade deposits in peralkaline igneous rocks. Competition with established Chinese HREE and Y sources and a developing Australian deposit will be a factor.     

Petrological and geochemical characteristics of Zhaibei granites in Nanling region,Southeast China: Implications for REE mineralization

Mineralization with ion adsorption rare earth elements (REEs) in the weathering profile of granitoid rocks from Nanling region of Southeast China is an important REE resource, especially for heavy REE (HREE) and Y. However, the Jurassic granites in Zhaibei which host the ion adsorption light REE (LREE) ores are rare. It is of peraluminous and high K calc-alkaline composition, which has similar geochemical features of high K₂O + Na₂O and Zr + Nb + Ce + Y contents and Ga/Al ratio to A-type granite. Based on the chemical discrimination criteria of Eby [Geology 20 (1992) 641], the Zhaibei granite belongs to A1-type and has similar source to ocean island basalts. The rock is enriched in LREE and contains abundant REE minerals including LREE-phosphates and halides. Minor LREE was also determined in the feldspar and biotite, which shows negligible and negative Eu anomalies, respectively. This indicates that the Zhaibei granite was generated by extreme differentiation of basaltic parent magmas. In contrast, granites associated with ion adsorption HREE ores contain amounts of HREE minerals, and show similar geochemical characteristics with fractionated felsic granites. Note that most Jurassic granitoids in the Nanling region contain no REE minerals and cannot produce REE mineralization. They belong to unfractionated M-, I- and S-type granites. Therefore, accumulation of REE in the weathering profile is controlled by primary REE mineral compositions in the granitoids. Intense fractional crystallization plays a role on REE enrichment in the Nanling granitoid rocks.     

Geochemistry, Geochronology and Lu-Hf Isotopes of Peraluminous Granitic Porphyry from the Walegen Au Deposit, West Qinling Terrane

Walegen Au deposit is closely correlated with granitic intrusions of Triassic age, which are composed of granite and quartz porphyries. Both granite porphyry and quartz porphyry consist of quartz, feldspar and muscovite as primary minerals. Weakly peraluminous granite porphyry(A/CNK=1.10–1.15) is enriched in LREE, depleted in HREE with Nb-Ta-Ti anomalies, and displays subduction-related geochemistry. Quartz porphyry is strongly peraluminous(A/CNK=1.64–2.81) with highly evolved components, characterized by lower TiO_2, REE contents, Mg~#, K/Rb, Nb/Ta, Zr/Hf ratios and higher Rb/Sr ratios than the granite porphyry. REE patterns of quartz porphyry exhibit lanthanide tetrad effect, resulting from mineral fractionation or participation of fluids with enriched F and Cl. LAICP-MS zircon U-Pb dating indicates quartz porphyry formed at 233±3 Ma. The ages of relict zircons from Triassic magmatic rocks match well with the detrital zircons from regional area. In addition, ε_(Hf)(t) values of Triassic magmatic zircons from the granite and quartz porphyries are -14.2 to -9.1(with an exception of +4.1) and -10.8 to -8.6 respectively, indicating a crustal-dominant source. Regionally, numerous Middle Triassic granitoids were previously reported to be formed under the consumption of Paleotethyan Ocean. These facts indicate that the granitic porphyries from Walegen Au deposit may have been formed in the processes of the closing of Paleotethyan Ocean, which could correlate with the arc-related magmatism in the Kunlun orogen to the west and the Qinling orogen to the east.     

Rare Earth Elements in Coal-Bearing Deposits: Distribution Features and Geochemical Significance

The examination of Lower Cretaceous coals and clayey fractions of terrigenous host rocks of the Zyryanka Basin has revealed a generally negative type of the relative REE distribution (with a predominance of LREE over HREE) and a similar behavior of Th and U. Analogous characteristics are typical for metamorphic and igneous rocks of intermediate composition dominating in the provenance. In terms of the concentration and distribution of REE, Th, and U coal-bearing terrigenous rocks of the Zyryanka Basin are close to Phanerozoic clays and silty sandstones of the Russian Platform, while coals of the Zyryanka Basin are similar to metal-free coals of various basins (Kizel, Pennsylvanian, and others). Average REE and Th contents in the studied coals are five times lower than those in host terrigenous rocks. The coals differ from these rocks by relatively elevated HREE concentrations largely due to adsorption mechanism of the HREE accumulation. Data obtained on the REE, Th, and U distribution in coals and clayey fractions of host rocks are of fundamental significance for the comparitive analysis of the behavior of these elements in metal-bearing coals of various basins.     

Hydrothermal Redistribution of Rare—Earth Elements in Pingxiang Dacite,Guangxi

Distribution of the rare-earth elements (REE) in dacite has been studied so as to get a better understanding of the migration behavior of REE during alteration. Both unaltered and altered samples were collected in an unpolluted area of Guangxi Zhuang Autonomous Region, southwest China. The REE concentrations were analyzed by ICP-MS. It is concluded that the REE were enriched during dacite alteration in varying degrees. The chondrite-normalized REE patterns of altered samples approximately maintain the characteristics of unaltered samples. However, if we normalize the REE concentrations of altered samples with unaltered dacite, fractionation of REE will appear. The LREE are more enriched than HREE in all altered samples with the LREE possibly precipitated as carbonate minerals. Both positive and negative Eu anomalies exist. Enrichment, immobility and depletion are noticed for the element Lu. Heavy mineral alteration, difference in stability constant between carbonate LREE and HREE complexes, downward migration of weathering fluid and microenvironment change may be responsible for the fractionation of REE in the altered dacite.     

辽北西丰地区宝兴岩体LA-ICP-MS锆石U-Pb年龄及岩石地球化学特征

宝兴岩体位于华北板块北缘陆缘活动带东段,岩性为花岗闪长岩,LA-ICP-MS锆石~(206)Pb/~(238)U年龄加权平均值为235.0±1.3Ma,属于中三叠世。岩石的K_2O/Na_2O平均值为1.07,属高钾钙碱性系列;富集大离子亲石元素,亏损高场强元素,具有活动陆缘钙碱性岩系特征;稀土元素总量平均值为147×10~(-6),稀土元素配分曲线右倾,属具中等负Eu异常的轻稀土元素富集、重稀土元素亏损型。通过岩石学、岩石地球化学及年代学研究,结合邻区构造演化研究,认为中三叠世研究区在伸展作用下岩石圈进行拆沉,从而形成大规模的岩浆活动。