Ionprobe U-Pb zircon ages from the high-pressure/low-temperature mélange of Syros, Greece: age diversity and the importance of pre-Eocene subduction

The Cycladic blueschist belt in the central Aegean Sea has experienced high‐pressure (HP) metamorphism during collisional processes between the Apulian microplate and Eurasia. The general geological and tectonometamorphic framework is well documented, but one aspect which is yet not sufficiently explored is the importance of HP mélanges which occur within volcano‐sedimentary successions. Unresolved issues concern the range in magmatic and metamorphic ages recorded by mélange blocks and the significance of eventual pre‐Eocene HP metamorphism. These aspects are here addressed in a U‐Pb zircon study focusing on the block–matrix association exposed on the island of Syros. Two gneisses from a tectonic slab of this mélange, consisting of an interlayered felsic gneiss‐glaucophanite sequence, yielded zircon ²⁰⁶Pb/²³⁸U ages of 240.1 ± 4.1 and 245.3 ± 4.9 Ma, respectively, similar to Triassic ages determined on zircon in meta‐volcanic rocks from structurally coherent sequences elsewhere in the Cyclades. This strongly suggests that parts of these successions have been incorporated in the mélanges and provides the first geochronological evidence that the provenance of mélange blocks/slabs is neither restricted to a single source nor confined to fragments of oceanic lithosphere. Zircon from a jadeitite and associated alteration zones (omphacitite, glaucophanite and chlorite‐actinolite rock) all yielded identical ²⁰⁶Pb/²³⁸U ages of c. 80 Ma. Similar Cretaceous U‐Pb zircon ages previously reported for mélange blocks have been interpreted by different authors to reflect magmatic or metamorphic ages. The present study adds a further argument in favour of the view that zircon formed newly in some rock types at c. 80 Ma, due to hydrothermal or metasomatic processes in a subduction zone environment, and supports the interpretation that the Cycladic blueschist belt records both Cretaceous and Eocene HP episodes and not only a single Tertiary HP event.     

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.     

藏北新生代两套钾玄质火山岩系列地球化学特征

岩石学和元素地球化学特征研究表明，藏北新生代自南向北沿可可西里岩带和喀喇昆仑—玉门岩带出露有两套钾玄质系列火山岩。它们富集大离子亲石元素(LILE)和轻稀土(LREE)及明显亏损Nb—Ta—Ti，同时具有板内和岛弧(陆弧)的双重特征。源区来源于可能与俯冲带流体有关的相似交代富集地幔，成岩过程主要经历了低度(＜10％)辉石分离结晶作用，同时，源区伴有地壳物质的混染作用。     

中国东部苏鲁榴辉岩超基性岩褶皱带的演化及其与大别(中国)和柯切塔夫(哈萨克斯坦)杂岩的对比(英文)

苏鲁褶皱带形成于元古宙 (2 2 33～ 185 5Ma)典型优地槽构造环境 ,主要由石榴橄榄岩、石榴辉石岩、榴辉岩等侵入岩 (柯石英深度相地幔岩浆房中形成 )和它们的火山沉积建造围岩一起经褶皱、变质而形成。变质作用经历了先蓝片岩相 (前花岗岩 )后片麻岩混合岩相过程。由于变质作用的不规律性 ,苏鲁褶皱带可分为 2个构造带 :(1)东部构造带 (蓝片岩 )和 (2 )西部构造带 (片麻岩混合岩 )。根据A·都城秋穗所识别的变质带系统 ,可将其作为一个双变质带。东部构造带以出现许多块状、条带状榴辉岩辉石岩橄榄岩组合的残余岩块为特征 ,其中还残留着高压的矿物 (石榴石、绿辉石、柯石英 ) ,而且有被混合岩和各种交代岩替代的显著标志。在中生代 ,苏鲁元古褶皱带受造山作用的影响活化 ,导致许多花岗岩体的侵入 ,使交代岩广泛发育。     

Petrological feature of spinel lherzolite xenolith from Oki-Dogo Island: An implication for variety of the upper mantle peridotite beneath southwestern Japan

Abstract   Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo₈₆) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism.     

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.     

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。     

地壳流体与地幔流体间的关系

通过铀、金矿床及地幔岩捕虏体研究，初步得出以下认识：（１）在热液作用中岩浆分异热液是不存在的；（２）碱交代作用是整个地幔交代作用和地壳交代作用的基本运作机制，现已构成有几十条具体规律的理论系统；碱交代岩是地幔流体转变为热液的化石记录；（３）拆离断层构造体系是地幔流体上升到地壳后的活动通道；（４）磷（Ｐ）是地幔流体的特征性示踪成分；（５）大洋缺氧事件、生物种属灭绝、厄尔尼诺等有共同的地幔流体致因；（６）天然气－油－盐－金属成矿是统一的热液成矿作用。软流体是今后区域成矿预测的重要新依据。软流体的顶部发育有次级、再次级的局部上凸部，这是矿带、矿田群的重要成矿控制因素和找矿新标志。     

地幔交代作用的微区微量元素证据——云南双沟蛇绿岩的质子探针研究

用质子探针技术对双沟地幔交代熔融物的微区微量元素进行了测定。研究表明,地幔橄榄岩中的残留矿物橄榄石和斜方辉石仅含Ni和Zn,而Ga、Ge、Sr、Rb、Zr、Y、As、Pb等微量元素主要集中在地幔部分熔融所产生的矿物(尤其是尖晶石和绿泥石)中。微区范围内微量元素的分布表明,尖晶石二辉橄榄岩地幔不均一性的尺度可达微米级,通常解释为尖晶石二辉橄榄岩在开放系统下地幔交代作用的结果。