四川木洛稀土矿床碳酸岩地球化学

木洛稀土矿床成因上与碳酸岩-碱性杂岩密切相关。碳酸岩主要由方解石组成,CaO/（CaO＋MgO＋FeO＋Fe2O3＋MnO）比值在95.7%～99.6%,为方解石碳酸岩。碳酸岩相对富集大离子亲石元素Ba、Sr、LREE,亏损高场强元素Nb、Ta、Ti、Zr、P,高Zr/Hf和La/Nb值,低Sm/Nd和Rb/Sr值,暗示岩石来自富集地幔EMI。地质、地球化学研究表明,木洛碳酸岩是在峨眉山地幔柱地幔遗存物经喜马拉雅造山运动再次活化的产物,但碳酸岩熔浆在上侵过程中受到地壳物质混染。碳酸岩-碱性岩熔浆带来大量稀土元素,并在喜马拉雅造山期造山运动派生的局部引张部位成矿。     

化学地层学研究中的若干注意事项

化学地层学因其交叉学科特点和研究对象的复杂性使得研究过程中任何一个环节的不足都将造成测试出现偏差,成果的可信度也将出现问题。高昂的成本也要求研究者把有限的资源集中到正确的目标上。近20年研究历程却恰恰将此类性质的问题陆续暴露了出来。如采样阶段获取原生性状考虑不充分或依据不足、测试阶段缺乏校验、数据分析阶段挖潜和综合利用有待完善以及化学岩、碎屑岩和生物岩各自的基础性和针对性研究有待提高等。有些问题带有相当程度的普遍性,有些甚至是严重的核心技术问题。笔者结合最新相关研究成果对上述问题进行了逐一分析和系统修正。     

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.     

Isotopic Ages of the Carbonatitic Volcanic Rocks in the Kunyang Rift Zone in Central Yunnan, China

The Mesoproterozoic Kunyang rift, which is located on the western margin of the Yangtze platform and the southern section of the Kangdian axis, is a rare massive Precambrian iron-copper polymetallic mineralization zone in China. The Mesoproterozoic Wulu (Wuding-Lufeng) basin in the middle of the rift is an elliptic basin controlled by a ring fracture system. Moreover, volcanic activities in the basin display zonation of an outer ring, a middle ring and an inner ring with carbonatitic volcanic rocks and sub-volcanic dykes discovered in the outer and middle rings. The Sm-Nd isochron ages have been determined for the outer-ring carbonatitic lavas (1685 Ma) and basaltic porphyrite of the radiating dyke swarm (1645 Ma) and the Rb-Sr isochron ages for the out-ring carbonatitic lavas (893 Ma) and the middle-ring dykes (1048 Ma). In combination of the U-Pb concordant ages of zircon (1743 Ma) in trachy-andesite of the corresponding period and stratum (1569 Ma) of the Etouchang Formation, as well as the Rb-Sr iso     

Petrogenesis of the Ulsan carbonate rocks from the south-eastern Kyongsang Basin, South Korea

Abstract The petrogenesis of the Ulsan carbonate rocks in the Mesozoic Kyongsang Basin of South Korea, which have previously been interpreted as limestone of Paleozoic age, is reconsidered in the present study. Within the Kyongsang Basin, a small volume of carbonate rocks, containing a magnetite deposit and spatially associated ultramafic rocks, is surrounded by sedimentary, volcanic and granitic rocks of the Mesozoic age. The simple cross‐cutting relationships and other outcrop features of the area indicate that the carbonate rocks are an intrusive phase and younger than the other surrounding Mesozoic rocks. The Ulsan carbonates have low concentrations of rare earth elements (REE) and trace elements with the carbon and oxygen isotope values in the range of δ¹³C_PDB = 2.4 to 4.0‰ and δ¹⁸O_SMOW = 17.0 to 19.5‰. Outcrop evidence and geochemical signatures indicate that the Ulsan carbonates were formed from crustal carbonate melts, which were generated by the melting/fluxing of crustal carbonate materials, caused by the emplacement‐related processes of alkaline A‐type granitic rocks. Compared to typical mantle‐derived carbonatites associated with silica‐undersaturated, strongly peralkaline systems, the relatively small size and geochemical characteristics of the Ulsan carbonates reflect carbonatite genesis in a silica‐saturated, weakly alkali intrusive system. Major deep‐seated tectonic fractures formed by the collapse of the cauldron or the rift system associated with the opening of the East Sea (Japan Sea) might have facilitated the ascent of the crustal carbonate melts.     

鲁中碳酸岩中磷灰石同位素地球化学研究

鲁中地区分布着100多个碳酸岩体，微量元素含量及稀土配分等均与世界典型碳酸岩相近。而碳酸岩的碳氧及斑晶磷灰石的锶、钛同位素组成与典型地幔物质有差异，与富集地幔颇为近似，从而证实在山东地区陆壳下存在富集地幔源区。     

滇中昆阳群火成碳酸岩的发现及其意义

在武定西矿带发现的已大理岩化的滇中昆阳群（Pt2k)火成碳酸岩富含钠长石、更长石、金云母、黑云母等硅酸盐矿物，发育火成结构构造，如斑状结构、隐晶结构，流纹构造、带状构造、气孔、杏仁构造等，与沉积围岩相比，岩石高Si、Al、Fe、Mg、Mn、P，富K2O Na2O，低钙，轻稀土富集，富含Nb、Zr、Hr、U、Th、Sr、Ba、稀土等不相容元素，与粗面质、粗安质等碱性硅酸盐岩共生。（铁）白云石（＞５０％）内，含有粗面南、碳酸质熔融包裹体；流体包裹体均一温度可达４５０℃以上。其发现证明滇中元古代曾有碳酸质岩浆活动。     

生物礁岩分类方案

本文系统地提出了一个生物礁岩分类的新方案。生物礁岩首先根据次生组分的有无分为原生礁岩和次生礁岩。次生礁岩根据次生组分来源分为骨源次生礁岩和礁源次生礁岩。次生礁岩的二级分类根据次生组分的含量进行。骨源次生礁岩分为骨屑岩和含骨屑礁（灰）岩、倒骨央和含倒骨礁（灰）岩；礁源次生礁岩分为礁屑岩和含礁屑礁（灰）岩。骨屑岩根据次生组分的粒度分为巨骨砾（屑灰）岩、骨砾（屑灰）岩、细骨砾（屑灰）岩、骨砂（屑灰）岩；     

Continuous Gradations among Primary Carbonatitic, Kimberlitic, Melilititic, Basaltic, Picritic, and Komatiitic Melts in Equilibrium with Garnet Lherzolite at 3-8 GPa

Multianvil melting experiments in the system CaO–MgO–Al₂O₃–SiO₂–CO₂(CMAS–CO₂) at 3–8 GPa, 1340–1800°C, involvingthe garnet lherzolite phase assemblage in equilibrium with CO₂-bearingmelts, yield continuous gradations in melt composition betweencarbonatite, kimberlite, melilitite, komatiite, picrite, andbasalt melts. The phase relations encompass a divariant surfacein P–T space. Comparison of the carbonatitic melts producedat the low-temperature side of this surface with naturally occurringcarbonatites indicates that natural magnesiocarbonatites couldbe generated over a wide range of pressures >2·5 GPa.Melts analogous to kimberlites form at higher temperatures alongthe divariant surface, which suggests that kimberlite genesisrequires more elevated geotherms. However, the amount of waterfound in some kimberlites has the potential to lower temperaturesfor the generation of kimberlitic melts by up to 150°C,provided no hydrous phases are present. Compositions resemblinggroup IB and IA kimberlites are produced at pressures around5–6 GPa and 10 GPa, respectively, whereas the compositionsof some other kimberlites suggest generation at higher pressuresstill. At pressures <4 GPa, an elevated geotherm producesmelilitite-like melt in the CMAS–CO₂ system rather thankimberlite. Even when a relatively CO₂-rich mantle compositioncontaining 0·15 wt % CO₂ is assumed, kimberlites andmelilitites are produced by <1% melting and carbonatitesare generated by even smaller degrees of melting of <0·5%. KEY WORDS: carbonatite; CO₂; kimberlite; melilitite; melt generation     

陕西华阳川铀多金属矿床黑云母~(40)Ar/~(39)Ar年龄及其地质意义

笔者采用Ar-Ar测年技术,获得华阳川铀多金属矿床碳酸岩中黑云母~(40)Ar/~(39)Ar坪年龄132.58±0.70 Ma,等时线年龄133.01±0.74 Ma,含黑云母闪石硫化物伟晶岩中黑云母的~(40)Ar/~(39)Ar坪年龄93.72±2.38 Ma,等时线年龄91.49±1.97 Ma。镜下特征显示,铌钛铀矿的形成晚于碳酸岩中的黑云母及含黑云母闪石硫化物伟晶岩中的黑云母。因此,铌钛铀矿的形成时间应晚于93.72±2.38 Ma。这表明成矿带内除了已知存在三叠纪碳酸岩型Mo-Pb矿和白垩纪斑岩型Mo矿的成矿过程之外,还存在早白垩世之后的岩浆热液型U-Nb-Ti成矿过程。