U-Pb dating and trace element of titanite and garnet as indicators of the age and ore-forming condition of skarn W deposit: A case study of the Xiaoyao W polymetallic deposit in southern Anhui,China.SCIEI北大核心CSCD

逍遥矿床是安徽南部新发现的大型钨多金属矿床,其精细的岩浆-热液时限及成矿作用仍不明确。本文对其开展了石榴子石和榍石的U-Pb年代学和微量元素分析,发现逍遥矿床发育多阶段榍石(岩浆榍石和热液榍石),岩浆榍石与石英、磁铁矿、长石共生,而热液榍石与石英、方解石、辉钼矿、黄铜矿关系密切。逍遥矿床中石榴子石和榍石中均具有一定的U含量,其中石榴子石中U含量较低(平均为15.9×10^(-6)),岩浆榍石和热液榍石的U含量较高(平均值大于100×10^(-6))。石榴子石和榍石U-Pb同位素定年结果显示成岩和W多金属矿化均形成于150Ma左右,指示W多金属矿化与花岗闪长岩密切相关。岩浆榍石、钾长石、石英、磁铁矿矿物组合指示逍遥成矿岩浆具有氧化性强和富水的特征。逍遥钨矿中的石榴子石以钙铁榴石为主且富集W、Sn特征,指示早期流体为氧化性流体。此外,热液榍石中HFSE元素的高度富集表明其成矿流体为富碱、富F的热液系统,为钨、铅、锌、铜、银、钼多金属的富集提供了有利热液条件。综上所述,石榴子石和榍石能够有效指示矽卡岩W矿的成矿时代和成岩成矿条件。     

云南哀牢山-红河剪切带新生代富碱侵入岩中榍石年代学和地球化学特征

榍石作为副矿物在哀牢山-红河剪切带新生代富碱侵入岩中广泛存在。原位获取榍石矿物内部微量元素、U-Pb年龄和Sm-Nd同位素的空间变化对获取矿物和岩石的成因演化信息具有重要意义。本文使用四级杆/多接收电感耦合等离子体质谱（Quadrupole/Multi-Collector Inductively Coupled Plasma Mass Spectrometry,Q/MC-ICP-MS）与激光剥蚀系统（Laser Ablation,LA）联用,对哀牢山-红河剪切带5个富碱侵入岩体（桃花岩体、宁蒗-永胜岩体、哈播岩体、铜厂岩体和十里村岩体）中榍石开展了微区原位微量元素、U-Pb年代学和Sm-Nd同位素研究。微量元素分析结果表明,三江富碱侵入岩中榍石为岩浆成因,亏损Rb、Ba、Pb、Sr等大离子亲石元素,富集Th、U、Nb、Ta、Zr、Hf等高场强元素。榍石的稀土配分图均表现为明显右倾,不具有或具有弱的Eu负异常。与云南北衙、马厂箐矽卡岩矿床中的热液榍石相比,本文榍石在稀土元素组成上,具有较高的稀土元素总量、较高的Th/U、LREE/HREE和Ce/Ce^*比值,具有较低的Eu/Eu^*、Nb/Ta、Zr/Hf比值。微区原位LA-Q-ICP-MS U-Pb定年结果表明,研究区富碱岩体中榍石结晶年龄在32.5~37.9Ma之间,代表了岩体形成时代,与三江地区哀牢山-红河剪切带及其附近新生代富碱岩浆活动高峰期（~35Ma）一致,属于青藏高原晚碰撞期岩浆作用的产物。榍石微区原位LA-MC-ICP-MS Sm-Nd同位素分析结果显示,榍石颗粒的Nd同位素组成均一,表明榍石结晶过程中寄主岩浆的Nd同位素组成没有发生明显变化。各个富碱岩体之间的榍石Nd同位素组成变化范围在-6.8~-2.1之间,与全岩的同位素特征一致,表明榍石的原位微区Sm-Nd同位素可以作为富碱侵入岩研究中有效的示踪手段之一。

     

Granular titanite from the Roter Kamm crater in Namibia: Product of regional metamorphism,not meteorite impact

Accessory minerals with so-called granular texture have risen in importance as geochronological tools for U-Pb dating of meteorite impact events. Grain-scale recrystallization, typically triggered by a combination of high-strain deformation and post-impact heating, can create a polycrystalline microstructure consisting of neoblasts that expel radiogenic Pb, which are thus ideal for isotopic dating. While granular domains in zircon and monazite from shocked rocks have been demonstrated to preserve impact ages, few U-Pb dating studies have been conducted on granular microstructures in titanite (CaTiSiO₅). Here we report the occurrence of granular-textured titanite from ～2020 Ma granite basement rock exposed in the rim of the 4–5 Ma Roter Kamm impact structure in Namibia. Orientation mapping reveals two microstructurally distinct titanite populations: one consisting of strained/deformed grains, and the other consisting of grains that comprise aggregates of strain-free neoblasts. In situ U-Pb geochronology on 37 grains shows that most grains from both titanite populations yield indistinguishable U-Pb dates of ca. 1025 Ma, consistent with the observed microstructures forming during the Mesoproterozoic Namaqua Orogeny. Only four grains preserved older age domains, recording ca. 1875 Ma Paleoproterozoic metamorphism. Two significant observations emerge: (1) none of the analyzed titanite grains yield the 2020 Ma igneous crystallization age previously established from zircon in the same sample, and (2) no age-resetting was detected that could be attributed to the 4 to 5 Ma Roter Kamm impact event. Despite the similarity of the neoblastic microstructure to minerals from other sites with an established impact provenance, the granular texture and near-complete Pb-loss in titanite from Roter Kamm granite instead records a Paleo- to Mesoproterozoic polymetamorphic history, rather than Miocene age shock-related processes. These results highlight the critical importance of grain-scale context for interpretation of U-Pb data in granular titanite, and the potential for misinterpreting inherited (pre-impact) microstructures as impact-related phenomenon in target rocks with a complex geological history.     

Small-scale transport of trace elements Nb and Cr during growth of titanite: an experimental study at 600?°C, 0.4 GPa

Trace element distribution in titanite overgrowths on rutile has been investigated experimentally at 600?°C, 400?MPa and f_O2 near NiNiO buffer. Compositionally homogenous Cr- or Nb-doped synthetic rutile single crystals or Nb-containing natural rutile crystals were the source of Cr, Nb and Ti to synthesize titanite using the double-capsule technique. All element exchange with the source of Si, Ca and Al occurred via a NaCl–H₂O fluid. Titanite forms quickly and exclusively around the rutile crystals. The titanite overgrowth separates rutile from the bulk fluid, and all elements from rutile dissolution have to pass through the titanite rim. Trace element concentrations in titanite show a considerable scatter in experiments with and without Al, although the average concentrations of Cr or Nb of titanite around compositionally homogeneous synthetic rutile approach the expected values for closed system conditions. Variability of Al with Cr or Nb in the titanite is not correlated. The Al zoning is irregular and patchy, and also the distribution of trace elements does not show systematic trends in the spatial distribution. In experiments using zoned natural rutile, the concentrations of Nb in titanite are related to the Nb zoning in rutile, but the contents also vary unsystematically. Under the controlled conditions of the experiment, the explanation for the strongly irregular spatial distribution is most likely due to variations in elemental concentrations during transport from the rutile along the titanite grain boundaries. The transport pathway is complex because grain boundary migration is important during titanite growth. Such irregular element distribution is also found in a natural sample of titanite overgrowth on rutile from an eclogite with retrograde overprint in the amphibolite facies. Transport of Ti and trace elements was focused on grain boundaries and shielded from the rutile as a source of these elements. We conclude that this type of zoning is not related to changes in P–T or composition in an open system, but solely controlled by transport in and through the titanite rim.     

湖南杏枫山钨矿床热液榍石的地球化学特征、U-Pb定年及其地质意义

杏枫山钨矿床是湘中地区近年新发现的、产出于浅变质岩系中的矽卡岩型钨矿。本文通过电子探针与LA-ICP-MS等技术手段,对杏枫山矿区矽卡岩中的热液榍石进行了主、微量元素组成以及U-Pb年代学研究。研究表明,榍石具有以下特征：(1)较低的∑REE、TiO₂含量,极低的Th/U,以及较高的Al₂O₃和F含量,这些均为典型热液榍石的地球化学特征;(2)富W而亏损Mo,表明其形成的热液流体具有富W贫Mo的特征;(3)稀土配分模式为左倾的、轻稀土显著亏损的重稀土富集型,正Ce、Eu异常表明其形成环境较为还原。此外,榍石原位U-Pb定年结果显示该矿形成于215.2±2.7Ma,与邻近白马山钛铁矿花岗岩形成的时间一致,基于地质及年代学证据,我们认为该矿的形成与白马山印支期的岩浆热液活动有关。结合前人的研究结果,我们发现湘中地区钨成矿与印支期还原性花岗质岩浆岩密切相关,为湘中印支晚期区域性成矿作用的产物。

     

变基性岩部分熔融过程中榍石的微量元素效应:以南迦巴瓦混合岩为例

南迦巴瓦地区广泛出露的中下地壳变基性岩部分熔融形成的层状混合岩和淡色花岗岩,为研究部分熔融过程中榍石的地球化学行为对熔体的微量元素组成的影响提供了良好的机会。相对于源岩或熔融残留体,淡色体亏损Ti、V、REE、Y、Nb、Ta、U等元素,与混合岩中榍石的微量元素特征互补。混合岩、淡色体和榍石微量元素特征表明南迦巴瓦角闪岩部分熔融形成的淡色体的微量元素特征主要受控于榍石的地球化学行为。角闪岩脱水部分熔融过程中,由于长英质熔体的低Ti溶解度,榍石以未熔残留体形式存在于暗色体中,导致熔体亏损Ti、REE、Nb、Ta、V、U等元素和Sr/Y比值相对升高。关键元素在榍石和熔体之间的配分系数受熔体成分影响明显。角闪岩中变质榍石D_Nb/Ta < 1,因此变质榍石残留导致熔体Nb/Ta相对于源岩升高;而高Si-Al花岗质熔体中榍石D_Nb/Ta>1,因此与高Si-Al熔体平衡的榍石的分离（转熔或结晶分异）将导致熔体Nb/Ta比值相对源岩降低。榍石在部分熔融过程中的微量元素效应为理解变基性岩部分熔融产生熔体的地球化学特征提供新的认识。

     

U-Pb SHRIMP-II ages of titanite and timing constraints on apatite-nepheline mineralization in the Khibiny and Lovozero alkaline massifs (Kola Peninsula)

Results of this study of titanite samples collected from silicate rocks and apatite-nepheline-(sphene) ores from Paleozoic polyphase alkaline nepheline syenite complexes of the Khibiny and Lovozero massifs revealed the possibility of their in-situ U-Pb dating using sensitive high-resolution ion microprobe SHRIMP-II with an accuracy of 1.0-1.5%, which is comparable with that of U-Pb zircon analysis. Employing different approaches to age determination of the formation of the U-Pb system of titanites, the combined isochrons and mixing lines were plotted from the data obtained from the differentiated complex samples (121 analyses of five Khibiny samples and 52 analyses of one Lovozero sample) and apatite-nepheline ores (120 analyses of five Khibiny samples and 88 analyses of three Lovozero samples). They indicate synchronous crystallization of titanite in silicate rocks throughout the complexes: 374.1 ± 3.7 Ma for the Khibiny massif and 380.9 ± 4.5 Ma for the Lovozero massif, and attest to the later formation of phosphate-rare-metal ores: 371.0 ± 4.2 and 361.4 ± 3.2 Ma, respectively. The relatively delayed ore mineralization specific to the Lovozero massif can be accounted for the significantly lower volumes of magmatic melt and ore fluid involved, different thermal conditions, and the pattern of the investigated mineralization. As such, the obtained U-Pb data from titanite make it possible to limit significantly the time interval (most likely, not exceeding 15-20 Ma) comprising the evolution and activity of the ore-magmatic system of major agpaitic complexes, which is probably associated with plume magmatism.     

A new method integrating high-precision U-Pb geochronology with zircon trace element analysis (U-Pb TIMS-TEA)

Increased precision in isotope-dilution thermal ionization mass spectrometry (ID-TIMS) U-Pb geochronology has revealed age complexities in zircon populations that require new tools for understanding how the growth of zircon is related to geologic processes. U and Pb are routinely separated from other elements in dated minerals by ion exchange separation prior to TIMS isotope measurement. We develop a method in which trace elements in the exact same volume of zircon are redissolved and analyzed using solution nebulization inductively coupled plasma sector-field mass spectrometry with matrix-matched external liquid calibration. Using <0.5 ml solution, resulting concentrations are between <1 ppt for elements such as Ti, Nb and Ta and tens of ppb for Zr. By analyzing a series of standard solutions, zircons and procedural blanks, we show that accurate measurements are performed on Zr, Hf, Y, Sc, and the HREE while low-concentration elements can be measured accurately to <5 ppt. We performed combined U-Pb ID-TIMS geochronology with trace element analysis (here called U-Pb TIMS-TEA) on zircons from eight volcanic rocks comprising several volcanic systems and one metamorphic sample. Similar to previous in situ trace element analyses, zircon geochemistry is distinct between different samples and records petrogenetic processes such as fractional crystallization, assimilation and/or magma mixing. Unique from in situ analysis, U-Pb TIMS-TEA can trace geochemical evolution in accessory minerals with adequate age precision to resolve magmatic processes in rocks at least 200 million years old. This provides a means to identify auto-, ante- and xenocrystic zircon and lead to more robust age interpretations in ID-TIMS U-Pb geochronology. One suite of Cretaceous andesitic zircons shows correlations in geochemistry and absolute time that record evolution of a magmatic system over ∼250 ka prior to eruption. Future work will combine U-Pb TIMS-TEA with solution isotopic analysis of Nd, Sr and Hf and will be applied to a host of datable minerals such as monazite, sphene, apatite, rutile, xenotime, and baddeleyite. These combined tools will provide access to an improved understanding of a wide range of igneous and metamorphic processes as a function of time.     

Origin and timing of the post-Variscan gabbro–granite complex of Porto (Western Corsica)

The post-Variscan complex of Porto consists of metaluminous to slightly peraluminous A-type biotite granites mingled with gabbro-dioritic rocks, and late dykes with basaltic to trachyandesitic composition. U-Pb zircon dating by LA-ICP-MS on two mafic intrusive samples constrains the time of the gabbro–granite crystallisation at 281 ± 3 Ma and 283 ± 2 Ma. Hornblende ⁴⁰Ar-³⁹Ar ages from a late trachyandesite dyke date the dyking event at 280 ± 2 Ma, which is within error the U-Pb zircon ages of the intrusives. Biotite granites show variable major and trace element compositions and similar initial ε_Nd (−0.3 to +0.9). Whole rock chemistry variations and trace element compositions of plagioclase and allanite indicate that the granites are genetically linked, essentially through fractional crystallisation of feldspars and minor allanite. On the basis of whole-rock chemistry e.g. initial ε_Nd +4.9 to +1.7 and trace element clinopyroxene compositions, we have ascertained that the mafic intrusives and basic dykes formed from isotopically depleted mantle source-derived melts with similar trace element signature. These basic melts experienced slightly different evolutionary histories, controlled by fractional crystallisation and crustal contamination, mainly by the acid magma that gave rise to the associated biotite granites, but also by the enclosing older Variscan granitoids. U-Pb zircon data suggest that the Porto complex was affected by hydrothermal fluid circulation at 259 ± 9 Ma.     

U-Pb monazite ages in amphibolite- to granulite-facies orthogneiss reflect hydrous mineral breakdown reactions: Sveconorwegian Province of SW Norway

In the Rogaland–Vest Agder terrain of the Sveconorwegian Province of SW Norway, two main Sveconorwegian metamorphic phases are reported: a phase of regional metamorphism linked to orogenic thickening (M1) and a phase of low-pressure thermal metamorphism associated with the intrusion of the 931 ± 2 Ma anorthosite-charnockite Rogaland igneous complex (M2). Phase M1 reached granulite facies to the west of the terrane and M2 culminated locally at 800–850 °C with the formation of dry osumilite-bearing mineral associations. Monazite and titanite U-Pb geochronology was conducted on 17 amphibolite- to granulite-facies orthogneiss samples, mainly from a suite of 1050 ⁺²/₋₈ Ma calc-alkaline augen gneisses, the Feda suite. In these rocks, prograde negatively discordant monazite crystallized during breakdown of allanite and titanite in upper amphibolite facies at 1012–1006 Ma. In the Feda suite and other charnockitic gneisses, concordant to slightly discordant monazite at 1024–997 Ma probably reflects breakdown of biotite during granulite-facies M1 metamorphism. A spread of monazite ages down to 970 Ma in biotite ± hornblende samples possibly corresponds to the waning stage of this first event. In the Feda suite, a well defined monazite growth episode at 930–925 Ma in the amphibolite-facies domain corresponds to major clinopyroxene formation at the expense of hornblende during M2. Growth or resetting of monazite was extremely limited during this phase in the granulite-facies domain, up to the direct vicinity of the anorthosite complex. The M2 event was shortly followed by cooling through ca. 610 °C as indicated by tightly grouped U-Pb ages of accessory titanite and titanite relict inclusions at 918 ± 2 Ma over the entire region. A last generation of U-poor monazite formed during regional cooling below 610 °C, in hornblende-rich samples at 912–904 Ma. This study suggests: (1) that monazite formed during the prograde path of high-grade metamorphism may be preserved; (2) that monazite ages reflect primary or secondary growth of monazite linked to metamorphic reactions involving redistribution of REEs and Th, and/or fluid mobilisation; (3) that the U-Pb system in monazite is not affected by thermal events up to 800–850 °C, provided that conditions were dry during metamorphism. Received: 9 January 1997 / Accepted: 15 April 1998     

Rare earth element partitioning between titanite and silicate melts: Henry’s law revisited

We present detailed experimental results on the partitioning of rare earth elements (REE) between titanite and a range of different silicate melts. Our results show that Henry’s law of trace element partitioning depends on bulk composition, the available partners for heterovalent substitution, crystal composition, and melt composition. We illustrate that the partition coefficients for Sm depend very strongly on the bulk concentration of Sm in the system. The substitution mechanism, by which rare earth elements are incorporated into the crystal structure, plays an important role for trace element partitioning and also for the onset of Henry’s law. Our data show that there are clear differences between substitution mechanisms of major elements compared to elements which are present only as traces. Our experiments also clearly show that the onset of Henry’s law depends on the concentrations of the sum of all trace elements which are incorporated into the crystal by the same substitution mechanism. For geochemical modelling of magmatic processes involving titanite, and indeed other accessory phases, it is of crucial importance to first evaluate whether the REE, and other trace elements, are present as traces or as major elements, only then appropriate D values may be chosen.     

Re-evaluating monazite as a record of metamorphic reactions

This study presents a re-examination of historical specimens (DG136 and DG167) from the Monashee complex in the southeastern Canadian Cordillera that are critical to the current understanding of rare earth element (REE) distribution between garnet and monazite (and other accessory minerals) during metamorphism. Nine-hundred and fifty-one new monazite petrochronology spot analyses on 29 different grains across two specimens outline detailed (re)crystallization histories. Trace element data collected from the same ablated volume, interpreted in the context of new phase equilibria modelling that includes monazite, xenotime and apatite, link ages to specific portions of the pressure–temperature (P-T) paths followed by the specimens. These linkages are further informed by garnet Lu-Hf geochronology and xenotime petrochronology. The clockwise P-T paths indicate prograde metamorphism was ongoing by ca. 80 Ma in both specimens. The structurally deeper specimen, DG136, records peak P-T conditions of ~755–770 ℃ and 8.8–10.4 kbar, interpreted to coincide with (re-)crystallization of low Y monazite at ～75–70 Ma. Near-rim garnet isopleths from DG167 cross in the observed peak assemblage field at ～680 °C and 9.3 kbar. These conditions are interpreted to correspond with low Y monazite (re-)crystallisation at ～65 Ma. Both specimens record decompression along their retrograde path coincident with high Y 70–55 Ma and 65–55 Ma monazite populations in DG136 and DG167, respectively. These findings broadly agree with those initially reported ～20 years ago and confirm early interpretations using trace elements in monazite as generally reliable markers of metamorphic reactions. Modern phase equilibria modelling and in situ petrochronological analysis, however, provide additional insight into monazite behaviour during anatexis and the effects of potential trace element buffering by REE-bearing phases such as apatite.     

锆石铀-铅定年激光剥蚀-电感耦合等离子体质谱原位微区分析进展

激光剥蚀-电感耦合等离子体质谱(LA-ICP-MS)技术是目前最常用的锆石U-Pb同位素年龄测定方法之一。该方法能够对单颗粒锆石内部年龄差异实现快速、准确的原位微区分析。文章总结了近年来激光剥蚀系统、ICP-MS技术以及LA-ICP-MS锆石U-Pb定年方法、相关应用实例研究的进展和现状。系统评述了激光发生器,剥蚀池,剥蚀参数(激光波长、脉冲宽度、剥蚀气体、孔径大小)以及四极杆和扇形磁场质谱仪对锆石U-Pb年龄数据的精度和准确度的影响。详细介绍了基于锆石年龄标准样品、标准溶液及其他标样的外标定量校准方法,单个U/Pb比值计算方法,普通铅校正方法以及同位素年龄与微量元素同时测定的方法。目前LA-ICP-MS锆石U-Pb定年技术主要应用于碎屑锆石的沉积物源区示踪和岩浆事件的年代学约束研究。     

Stability of Al- and F-rich titanite in metacarbonate: petrologic and isotopic constraints from a polymetamorphic eclogitic marble of the internal Sesia Zone (Western Alps)

Al- and F-rich titanite (3.862O₃ <9.33 wt%, 0.931(F, OH)₁Ti_-1O_-1 substitution within single crystals, particularly at grain boundaries with omphacite and/or phengite. In-situ ion microprobe U-Pb analysis of titanite domains that have various Al and F contents yielded apparent ²⁰⁶Pb/²³⁸U ages scattering between 283 and 153 Ma. Chemical and petrological data are indispensable to interpret this complex age distribution, and the good correlation between ²⁰⁶Pb/²³⁸U ratios and Al content indicates that the Al- and F-rich titanite was formed during pre-Alpine metamorphism (𔕑ᆟ Ma). Progressively younger ages are obtained in domains with decreasing Al and F content, suggesting that partial chemical re-equilibration was responsible for the incomplete isotopic resetting during Alpine metamorphism. Petrological and U-Pb data show that Al- and F-rich titanite should be used with caution to infer high-pressure conditions in polymetamorphic carbonate systems.     

Crustal architecture above the high-pressure belt of the Grenville Province in the Manicouagan area: new structural, petrologic and U–Pb age constraints

Recent U–Pb age determinations and P–T estimates allow us to characterize the different levels of a formerly thickened crust, and provide further constraints on the make up and tectono-thermal evolution of the Grenville Province in the Manicouagan area. An important tectonic element, the Manicouagan Imbricate zone (MIZ), consists of mainly 1.65, 1.48 and 1.17 Ga igneous rocks metamorphosed under 1400–1800 MPa and 800–900 °C at 1.05–1.03 Ga, during the Ottawan episode of the Grenvillian orogenic cycle, coevally with intrusion of gabbro dykes in shear zones. The MIZ has been interpreted as representing thermally weakened deep levels of thickened crust extruded towards the NW over a parautochthonous crustal-scale ramp. Mantle-derived melts are considered as in part responsible for the high metamorphic temperatures that were registered.New data show that mid-crustal levels structurally above the MIZ are represented by the Gabriel Complex of the Berthé terrane, that consists of migmatite with boudins of 1136±15 Ma gabbro and rafts of anatectic metapelite with an inherited monazite age at 1478±30 Ma. These rocks were metamorphosed at about the same time as the MIZ (metamorphic zircon in gabbro: 1046±2 Ma; single grains of monazite in anatectic metapelite: 1053±2 Ma) and under the same T range (800–900 °C) but at lower P conditions (1000–1100 MPa). They are mainly exposed in an antiformal culmination above a high-strain zone, which has tectonic lenses of high P–T rocks from the MIZ and is intruded by synmetamorphic gabbroic rocks. This zone is interpreted as part of the hangingwall of the MIZ during extrusion. A gap of 400 MPa in metamorphic pressures between the tectonic lenses and the country rocks, together with the broad similarity in metamorphic ages, are consistent with rapid tectonic transport of the high P–T rocks over a ramp prior to the incorporation of the mafic lenses in the hangingwall.Between the antiformal culmination of the Gabriel Complex and the MIZ 1.48 Ga old granulites of the Hart Jaune terrane are exposed. They are intruded by unmetamorphosed 1228±3 Ma gabbro sills and 1166±1 Ma anorthosite. Hart Jaune Terrane represents relatively high crustal levels that truncate the MIZ-Gabriel Complex contact and are preserved in a synformal structure.Farther south, the Gabriel Complex is overlain by the Banded Complex, a composite unit including 1403+32/−25 Ma granodiorite and 1238+16/−13−1202+40/−25 Ma granite. This unit has been metamorphosed under relatively low-P (800 MPa) granulite-facies conditions. Metamorphic U–Pb data, limited to zircon lower intercept ages (971±38 Ma and 996±27 Ma) and a titanite (990±5 Ma) age, are interpreted to postdate the metamorphic peak.The general configuration of units along the section is consistent with extrusion of the MIZ during shortening and, finally, normal displacement along discrete shear zones.     

Petrogenesis of the microcrystalline-dioritic enclaves from Jiuling granitoids in the eastern segment of Jiangnan Orogen and constraints on magma source materials

Numerous dark enclaves with different shapes are found in Jiuling Neoproterozoic granitoids. Precise LA-ICP-MS U-Pb dating was conducted on zircons extracted from two microcrystalline enclave samples, yielding crystallization ages of 822.6±5.8 Ma and 822.2±6.2 Ma, respectively. The consistent ages within analytical errors with the host granitoids suggested that they were the products of the same magmatism. The microcrystalline-dioritic enclaves commonly show plastic forms and contain similar plagioclase megacrysts to the host rocks, and both of the enclaves and host granitoids showed a complex composition and structural imbalance in plagioclases. Furthermore, the apatites with a euhedral acicular shape occurred widely in the microcrystalline-dioritic enclaves. All of these petrographic features above imply magma mixing is involved in their diagenesis. The enclaves and host granitoids show a marked zircon trace element difference and Hf isotopic signatures without correlation in zircon trace element pairs but form their own system between enclaves and host granitoids. Additionally, most of the zircons show extremely high ε_Hf (t) with ε_Hf (t) =3.54–11.94 from the southern samples, and ε_Hf (t) =1.0–9.09 from the central region. Some zircons with the higher ε_Hf (t) are similar to the zircons from the juvenile island arc in the eastern segment of Jiangnan Orogen. Integrated geological and Hf isotopic characteristics suggest microcrystalline-dioritic enclaves were derived from the partial melting process of the Mesoproterozoic crust which enriched juvenile island arc materials and mixed with the granitic magma that remelted from the Mesoproterozoic continental crust which relatively enriched ancient sediments and mixed with the host granitoid in diagenesis.     

U–Pb evidence for a polyorogenic evolution of the HP–HT units of the NW Iberian Massif

. A isotope dilution thermal ionisation mass spectrometry U-Pb geochronological study was carried out on the high-pressure and high-temperature units (HP-HT units) overlying the oceanic suture in the Allochthonous Complexes of the NW Iberian Variscan Belt. The rocks investigated are seven granulite- to eclogite-facies paragneisses and one leucosome within mafic high-pressure granulites in the Ordenes and Cabo Ortegal Complexes of NW Spain. U-Pb dating of zircon, monazite, titanite and rutile reveal the presence of a pervasive Early Ordovician metamorphic event at ca. 500-480 Ma and a later Early Devonian event at ca. 400-380 Ma. The U-Pb ages, in conjunction with petrological and structural data, indicate that the high-pressure event recorded by these rocks is Early Ordovician in age. Monazite ages in the paragneisses suggest that peak metamorphic conditions were reached at ca. 500-485 Ma. Subsequently, the rock ensemble underwent exhumation accompanied by partial melting and zircon growth at ca. 485-470 Ma. Melting of mafic granulites was coeval with this latter episode as indicated by zircon crystallisation age in the leucosomes dated at ca. 486 Ma. Based on these data and on the general features of magmatism and metamorphic evolution, it is proposed that this process took place at a convergent plate boundary within a peri-Gondwanan oceanic domain. Monazite, titanite and rutile data in some of the samples studied show evidence of a second metamorphic episode that took place between ca. 400 and 380 Ma (with a peak at ca. 390-385 Ma). This Early Devonian event, at variance with the previous one, was not pervasive, but, rather, was localised in areas of intense Variscan tectonothermal reworking. It is claimed that this later metamorphic event was recorded by the U-Pb system in areas where monazite and titanite growth was enhanced by fluid circulation in highly strained rocks (Variscan shear zones). According to previous structural studies and Ar-Ar dating of fabrics, this Early Devonian episode took place as the HP-HT units were deformed and thrusted upon the ophiolitic units in the early stages of the Variscan collision.     

金红石-榍石转变过程中元素地球化学行为——以雅鲁藏布江缝合带角闪岩为例

金红石边缘形成榍石冠状边结构在变质中-基性岩中普遍存在,是金红石与退变质流体携带的SiO_2与CaO作用的结果,反应形成的榍石微量元素特征受到金红石和流体的共同影响。雅鲁藏布江缝合带中角闪岩LZ06-04在抬升过程经历近等温降压退变质作用,石榴子石分解导致同一样品中含石榴子石部分与不含石榴子石部分的退变质流体成分的差异。两种流体分别与金红石反应,对应形成的榍石具有相似的Nb、Ta含量和Nb/Ta比值特征,但截然不同的REE特征。榍石的Nb、Ta来源于金红石,残余金红石与含水流体再平衡Nb、Ta的分配系数增大,且D_(Nb)~(Rt/Fluid)≥D_(Ta)~(Rt/Fluid);虽然Nb和Ta在含水流体中都表现为不活动元素,但相对于Nb,Ta在含水流体中活动性较高。榍石的Zr-Hf体系特征受到锆石、石榴子石等矿物的综合影响,并且Zr-Hf在含水流体中表现出比Nb-Ta更高的活动性。榍石的REE特征受流体中REE特征、榍石与流体配分系数以及共生矿物的影响。在岩浆或变质体系,榍石形成过程中,REE富集矿物(如石榴子石、锆石、褐帘石、独居石、磷灰石等)形成或分解将影响榍石的REE分布特征或形成REE环带结构。含水流体中金红石退变质形成榍石反应的进行受流体中TiO_2、CaO和SiO_2活度的影响。因此榍石常见于钙碱性岩浆岩、富Ca基性变质岩和矽卡岩中。流体中CaO活度的变化影响榍石的形成,进而影响Ti、Nb、Ta在流体中的运移能力。俯冲板片产生流体在交代上覆富Ca地幔楔物质过程中形成榍石残留同样可以造成部分熔融体具有亏损HFSE特征。     

Phase-equilibrium constraints on titanite and rutile activities in mafic epidote amphibolites and geobarometry using titanite–rutile equilibria

Activities of titanite (Ttn, CaTiSiO₅) and/or rutile (Rt, TiO₂) phase components were calculated for 45 well‐characterized natural titanite‐ or rutile‐undersaturated epidote–amphibolites by using the equilibria: (i) 3 anorthite + 2 zoisite/clinozoisite + rutile + quartz = 3 anorthite + titanite + water (referred to as TZARS) and (ii) anorthite + 2 titanite = grossular + 2 rutile + quartz (referred to as GRATiS). In titanite‐bearing and rutile‐absent samples a_Rt is 0.75 ± 0.26. In titanite‐absent, rutile‐bearing samples a_Ttn is 0.89 ± 0.16. Mean values derived for a_Rt/a_Ttn are 0.92 ± 0.12 for rutile + titanite‐bearing samples and 0.42 ± 0.27 for samples lacking both titanite and rutile. Use of these values with TZARS yields pressure estimates for epidote–amphibolites that differ on average by <0.5 kbar from those recorded by established mineral barometers, even where both titanite and rutile are lacking. Despite rather large uncertainties in the average values obtained for a_Rt, a_Ttn or a_Rt/a_Ttn, application of TZARS yields pressure estimates that agree with independent estimates to within ±0.5 kbar for titanite‐ and/or rutile‐saturated samples, and to within ±0.8 kbar for samples that contain neither Ti‐phase. The accuracy and precision of the TZARS barometer are comparable to that of many well‐calibrated barometers. TZARS offers a much‐needed barometer for mafic rocks metamorphosed at epidote‐bearing amphibolite and blueschist facies conditions. In addition, the results provide a basis for application of other thermobarometers, such as Ti‐in‐zircon, where rutile activity is required as input.     

华北中部狐偃山杂岩体形成时代研究——来自榍石U-Pb同位素年代学的证据

近年随着定年技术的发展,榍石LA-ICP-MS U-Pb定年法逐渐被学者采用,用来揭示某些特殊岩石类型的形成时代,如碱性岩。华北中部狐偃山碱性杂岩体由多个侵入体组成,岩性主要为二长岩类,岩石中发育大量继承锆石,结晶锆石相对较少,但包含大量岩浆榍石。本次研究即利用榍石LA-ICP-MS U-Pb定年法,对研究相对薄弱的矿泉、狼窝沟2个二长岩体中榍石进行了年代学分析。结果表明这2个二长岩体分别侵位于129 Ma和130 Ma。作为对比,同时对相同2个样品进行了锆石LA-ICP-MS U-Pb定年,2种方法得到的结果在误差范围内一致。结合前人研究资料,狐偃山杂岩体主体二长岩类侵位于早白垩世早期（127~131 Ma）,早白垩世晚期（111~114 Ma）有少量正长岩形成,从而构成了狐偃山杂岩体。