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1.
Zircon textures and composition have been used to infer magmatic processes including closed-system fractional crystallization, magma mixing or replenishment, and country-rock assimilation. Here, we propose that zircon textures and composition may also be refractory recorders of magmatic volatile evolution. We present field, whole-rock chemical, textural, mineral chemical, and U–Pb age data from evolved, fine-to-coarse-grained granite intrusions on Melville Peninsula, Nunavut, Canada. Zircon forms two main populations in these granites, Type-1 and Type-2 zircon. Type-1 zircon is present in all samples, but predominant in fine-grained granite. Crystals are euhedral and inclusion-rich and show periodic, fine-scale oscillatory zoning, comparatively low concentrations of U (<2,200 ppm) and Hf (<1.6 wt%), high Zr/Hf (~40–62), and pervasive alteration. Type-2 zircon is predominant in coarse-grained granite. Crystals form overgrowths on Type-1 zircon and individual crystals. They are subhedral and inclusion-poor and show weak, irregular, large-scale oscillatory zoning, high U (up to ~7,250 ppm) and Hf (1.5–2.0 wt%), low Zr/Hf (~37–44), and only local alteration. Compatible trace-element concentrations and Zr/Hf change sharply across the boundary of Type-1 to Type-2 zircon; 207Pb/206Pb ages preclude a significant hiatus between crystallization of the two types. We argue against magmatic versus hydrothermal crystallization, country-rock assimilation, or magma mixing as causes for the crystallization of Type-1 and Type-2 zircon. We propose instead that Type-1 zircon formed from volatile-undersaturated magmas and that Type-2 zircon formed from volatile-saturated magmas. Magmas fractionated by volatile-driven filter pressing into crystal-rich mush and crystal-poor magma. Crystal-rich mush with abundant Type-1 zircon crystallized to fine-grained granite. Volatile-rich magma crystallized to Type-2 zircon and coarse-grained granite. While Type-1 zircon was pervasively altered by exsolving magmatic volatiles, Type-2 zircon was only locally affected by subsolidus hydrothermal alteration.  相似文献   

2.
Zoned crystals can be important recorders of magmatic processes in space and time. However, in most situations, the temporal dimension is difficult to quantify. Here, we have employed secondary ion mass spectrometry depth profiling to excavate parallel pits into non-polished crystal faces of zircon to obtain ~5 μm resolution U–Th disequilibrium ages (one pit) that can be correlated with trace element zoning at sub-μm resolution derived from a second pit. Data from 17 crystals representing each of the four rhyolite eruptions of Tarawera volcano, an intra-caldera edifice within the Okataina Volcanic Centre, reveal diverse zircon growth conditions over time. Most crystals display rimward depletions in Zr/Hf and Ti, broadly consistent with cooling and crystallization. However, a significant fraction of crystals lacks these patterns and displays rimward trace element variations consistent with isothermal or prograde crystallization. Oscillatory zonation patterns in Y, Th, and U are superimposed on the Zr/Hf and Ti trends. Despite the limited number of crystals analyzed in this way, the striking lack of ubiquitous trace element zoning patterns in crystals from the same hand sample implies that fractional crystallization upon cooling was punctuated by magma recharge and crystal mixing affecting different parts of the magma reservoir. By combining data from all crystals, a systematic change to more heterogeneous trace element abundances is revealed by zircon crystal domains <45 ka following the Rotoiti caldera-forming eruption. This contrasts with the more uniform conditions of zircon crystallization lasting >100 ka prior to caldera formation and is best explained by the post-caldera system consisting of small, isolated melt pockets that evolved independently. An important conclusion is that the zircon ‘cargo’ in volcanic rocks reflects thermally and compositionally divergent processes that act near simultaneously in a magma storage region and not exclusively the conditions in the eruptible magma.  相似文献   

3.
Protolith zircon in high‐grade metagranitoids from Queensland, Australia, partially recrystallized during granulite‐grade metamorphism. We describe the zircon in detail using integrated cathodoluminescence, U–Pb isotope, trace element and electron backscatter diffraction pattern (EBSP) analyses. Primary igneous oscillatory zoning is partially modified or obliterated in areas within single crystals, but is well preserved in other areas. A variety of secondary internal structures are observed, with large areas of transgressive recrystallized zircon usually dominant. Associated with these areas are recrystallization margins, interpreted to be recrystallization fronts, that have conformable boundaries with transgressive recrystallized areas, but contrasting cathodoluminescence and trace element chemistry. Trace element analyses of primary and secondary structures provide compelling evidence for closed‐system solid‐state recrystallization. By this process, trace elements in the protolith zircon are purged during recrystallization and partitioned between the enriched recrystallization front and depleted recrystallized areas. However, recrystallization is not always efficient, often leaving a ‘memory’ of the protolith trace element and isotopic composition. This results in the measurement of ‘mixed’ U–Pb isotope ages. Nonetheless, the age of metamorphism has been determined. A correlation between apparent age and Th/U ratio is indicative of incomplete re‐setting by partial recrystallization. Recrystallization is shown to probably not significantly affect Lu–Hf ages. Recrystallization has been determined by textural and trace element analysis and EBSP data not to have proceeded by sub‐grain rotation or local dissolution/re‐precipitation, but probably by grain‐boundary migration and defect diffusion. The formation of metamorphic zircon by solid‐state recrystallization is probably common to high‐grade terranes worldwide. The recognition of this process of formation is essential for correct interpretation of zircon‐derived U–Pb ages and subsequent tectonic models.  相似文献   

4.
Recrystallization of zircons under the influence of fluids was studied using examples from Precambrian rocks (microcline granites, metasedimentary, and mafic rocks) of the Kola Peninsula. All zircon crystals showed complex internal textures visible by cathodoluminescence and backscattered electron (BSE) imaging. Detailed mineralogical and geochemical studies with subsequent secondary ion mass spectrometer U–Pb dating of different zircon domains show that secondary texture formation can be interpreted in terms of metasomatic replacement of zircon crystals on the base of crystallogenetic experimental models. Mechanisms of zircon replacement and interpretation of U–Pb ages for secondary zircon domains are dependent on the degree of damage of the zircon structure and the fluid composition. The recrystallization of metamict zircon without additional supply of new zircon substance (Zr, SiO2) goes with the dissolution of amorphous domains and precipitation of new polycrystalline zircon, which preserves the U–Pb initial age, but loses radiogenic lead, and the lower intercept of Discordia lines with the Concordia curve determines the time of fluid influence. The recrystallization of metamict zircon or crystalline zircon with high contents of impurities with additional supply of Si and Zr forms monocrystalline replacements. Dissolution of primary zircon is accompanied by growth of new zircon domains differing in the composition of isomorphic impurities and zones of transitional composition, whose ages have no geological sense. The study is of particular importance for zircons from Precambrian rocks with long and complex histories.  相似文献   

5.
For magmatic rocks, it is often found that zircon 206 Pb/238 U and 207 Pb/235 U ratios continuously plot on the concordia line with a relatively large age span for the same sample, which gives rise to large dating errors or even unrealistic dating results. As the trace element concentrations of zircon can reflect its equilibrated magma characteristics, they can be used to determine whether all the analytical spots on the zircons selected to calculate the weighted mean age are cogenetic and formed in a single magma chamber. This work utilizes the results of zircon trace element concentrations and U-Pb isotopic analyses to explore the screening of reasonable U-Pb ages, which can be used to determine a more accurate intrusion crystallization age. The late Mesozoic Huayuangong granitic pluton complex, which is located in the Lower Yangtze region, eastern China, was selected for a case study. The Huayuangong pluton comprises the central intrusion and the marginal intrusion. Two samples from the marginal intrusion yielded consistent zircon weighted mean 206 Pb/238 U ages of 124.6 ± 2.0 Ma and 125.9 ± 1.6 Ma. These analytical spots also exhibit Zr/Hf and Th/U ratios concordant with the evolution of a single magma, from which the dated zircons crystallized. However, for the central intrusion, the analytical spots on zircons from two samples all show a continuous distribution on the concordia line with a relatively large age span. For each sample from the central intrusion, the zircon Zr/Hf ratios do not conform to a single magma evolutionary trend, but rather can be divided into two groups. We propose that zircon Zr/Hf ratios can provide a new constraint on U-Pb zircon dating and zircon Th/U ratios can also be used as a supplementary indicator to constrain zircon dating and determine the origins of the zircons and whether magma mixing has occurred. By screening zircon analytical spots using these two indicators, the two samples from the central intrusion of the Huayuangong pluton produce results of 122.8 ± 4.3 Ma and 122.9 ± 2.2 Ma, which are consistent with the field observations that the central intrusion is slightly younger than the marginal intrusion.  相似文献   

6.
The 176Hf/177Hf composition of inherited and magmatic zircon in the 538 Ma S-type Peninsula pluton (South Africa) has been determined at different scales. In the smallest rock samples investigated (<0.5 dm3), as well as within individual thin sections, magmatic zircon crystals exhibit the same wide range in εHf(538) as the pluton (8ε units). In addition, across a significant range of bulk-rock compositions, both the range and average of the magmatic zircon Hf isotopic composition do not vary significantly with compositional parameters that are expected to scale with the proportion of mantle-derived magma addition (e.g., Mg# and Ca). At all scales, the εHf variability in the magmatic zircon fraction matches well with that portrayed by the time-evolved inherited zircon population [i.e., with the εHf(538) range of the inherited zircon cores]. This evidence suggests that the εHf heterogeneity of magmatic zircon is directly inherited from the source. However, the analysis of zircon core–rim pairs reveals that the 176Hf/177Hf composition of the inherited crystals does not directly transfer to their magmatic overgrowths. Small-scale modeling of zircon dissolution and re-precipitation in a static magma generates sub-mm melt domains having variable Zr content and Hf isotope composition. The composition of these domains is controlled by the size and isotope composition of the nearest dissolving zircon crystals and the cooling rate of the magma. These results suggest that in magma systems with a substantial inherited zircon load, zircon crystals within the same rock should record variable 176Hf/177Hf in the magmatic zircon fraction.  相似文献   

7.
Two populations of kimberlitic zircon are present in the Timber Creek kimberlites, Northern Territory. Laser ablation ICP MS U—Pb dating yields an age of 1483 ± 15 (2σ) Ma for the main group and an age of 179 ± 2 Ma for the other group. This distinction of two age groups is strongly supported by Hf isotope data on the same zircons. Although the trace element patterns of both populations are typical of mantle derived zircons, the ‘young’ population has slightly higher concentrations of most trace elements, but has lower Hf, Nb, Ta and Pb contents. The distinct differences in trace element contents and Hf isotopic composition of the two zircon populations indicate that they were derived from different magma sources. The dating results indicate that the emplacement age of the Timber Creek kimberlites cannot be older than the age of the ‘young’ zircon population (i.e. 179 ± 2 Ma). This clarifies the inconsistency between the previously reported SHRIMP age of the Timber Creek zircons (1462 ± 53 Ma) and the much younger age (1200 Ma) of the sediments of the Victoria River Basin into which these kimberlites have intruded. The Timber Creek kimberlites are a newly recognised extension of the widespread Jurassic kimberlite activity known in Western Australia and South Australia (Wandagee, Orroroo, Cleve and Eurelia kimberlites).  相似文献   

8.
Extreme enrichment of Sb, Tl and other trace elements in altered MORB   总被引：2，自引：0，他引：2  
We have analyzed 25 trace elements (e.g., Sb, Tl, Sn, rare earth elements (REE), Th, U, Nb, Pb, Zr, Hf, and Y) in altered mid-ocean ridge basalts (MORB) from locations near the mouth of the Gulf of California. Our results imply that the heavy REE and Y are not seriously affected by seawater alteration, in agreement with previous studies. The elements Zr, Hf, Nb, light REE and Sr are enriched up to a factor of 2 in some extremely altered samples. However, element ratios between Zr, Hf, and Nb (e.g., Zr/Hf, and Zr/Nb) are not greatly affected, presumably due to the chemical similarity of these elements during any exchange process. The enrichment of Th and Sn is even higher. Antimony, Tl, Cs, Rb, Rb, and Ba are most easily altered by water-rock interaction and are therefore the best indicators for seawater alteration. The enrichment factor of the most mobile element Sb is up to 2000.

There is a weak correlation between the concentration in seawater and the enrichment factors. On the other hand, the worldwide pelagic clay pattern matches the enrichment pattern much more closely, and the limited data available for local oceanic sediments give an even better correlation. A plausible model to explain the enrichment pattern may be an elemental exchange between basalt and seawater that had interacted earlier with overlying sediments.  相似文献   


9.
A potential zircon reference material (BB zircon) for laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) U‐Pb geochronology and Hf isotope geochemistry is described. A batch of twenty zircon megacrysts (0.5–1.5 cm3) from Sri Lanka was studied. Within‐grain rare earth element (REE) compositions are largely homogeneous, albeit with some variation seen between fractured and homogeneous domains. Excluding fractured cathodoluminescence bright domains, the variation in U content for all analysed crystals ranged from 227 to 368 μg g?1 and the average Th/U ratios were between 0.20 and 0.47. The Hf isotope composition (0.56–0.84 g/100 g Hf) is homogeneous within and between the grains – mean 176Hf/177Hf of 0.281674 ± 0.000018 (2s). The calculated alpha dose of 0.59 × 1018 g?1 for a number of BB grains falls within the trend of previously studied, untreated zircon samples from Sri Lanka. Aliquots of the same crystal (analysed by ID‐TIMS in four different laboratories) gave consistent U‐Pb ages with excellent measurement reproducibility (0.1–0.4% RSD). Interlaboratory assessment (by LA‐ICP‐MS) from individual crystals returned results that are within uncertainty equivalent to the TIMS ages. Finally, we report on within‐ and between‐grain homogeneity of the oxygen isotope systematic of four BB crystals (13.16‰ VSMOW).  相似文献   

10.
With the aim of better understanding geochemistry of coal, 71 Late Permian whole-seam coal channel samples from western Guizhou Province, Southwest China were studied and 57 elements in them were determined. The contents of Al, Ca, Co, Cr, Cu, Fe, Ga, Hf, K, Li, Mn, Mo, Nb, Ni, Sn, Ta, Ti, Th, U, V, Zr, and REEs in the Late Permian coals from western Guizhou Province are higher than the arithmetic means for the corresponding elements in the US coals, whereas As, Ba, Br, F, Hg, P, Se, and Tl are lower. Compared to common Chinese coals, the contents of Co, Cr, Cu, Ga, Hf, Li, Mn, Mo, Ni, Sc, Sn, Ti, U, V, Zn, and Zr in western Guizhou coals are higher, and As, F, Hg, Rb, Sb, Tl, and W are lower. Five groups of elements may be classified according to their mode of occurrence in coal: The first two, Group A, Tm–Yb–Lu–Y–Er–Ho–Dy–Tb–Ce–La–Nd–Pr–Gd–Sm, and Group B, As–Sr–K–Rb–Ba–F–Ash–Si–Sn–Ga–Hf–Al–Ta–Zr–Be–Th–Na, have high positive correlation coefficients with ash yield and they show mainly inorganic affinity. Some elements from Group B, such as Ba, Be, Ga, Hf, and Th, are also characterized by significant aluminosilicate affinity. In addition, arsenic also exhibits high sulfide affinity (rS–Fe>0.5). The elements, which have negative or lower positive correlation coefficients with ash yield (with exceptions of Bi, Cs, Nb, Mn, Se, and Ti), are grouped in other four associations: Group C, Cr–V–Mo–U–Cd–Tl; Group D, Hg–Li–Sc–Ti–Eu–Nb–Cs–W; Group E, Bi–Sb; and Group F, Co–Ni–Cu–Pb–Zn–Mg–Se–Ca–Mn–S–Fe. The correlation coefficients of some elements, including Co, Cr, Cu, Fe, Hg, Li, Mo, Ni, P, S, Sc, U, V, and Zn, with ash yield are below the statistically significant value. Only Cr and Cu are negatively correlated to ash yield (−0.07 and −0.01, respectively), showing intermediate (organic and inorganic) affinity. Manganese and Fe are characterized by carbonate affinity probably due to high content of epigenetic veined ankerite in some coals. Phosphorus has low correlation coefficients with any other elements and is not included in these six associations. There are five possible genetic types of enrichment of elements in coal from western Guizhou Province: source rock, volcanic ash, low-temperature hydrothermal fluid, groundwater, and magmatic hydrothermal inputs.  相似文献   

11.
Partition coefficients of Hf,Zr, and REE between zircon,apatite, and liquid   总被引：25，自引：2，他引：25  
Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10–100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite.  相似文献   

12.
Garnet–clinopyroxene ultra‐high‐pressure (UHP) rocks from the northern Bohemian Massif contain zircon with micro‐diamond inclusions. Trace element concentrations, oxygen and hafnium isotopic composition and U–Pb age of distinct textural domains in zircon characterize their growth conditions and temporal evolution. Diamond‐bearing zircon mantle domains with relicts of oscillatory zoning have uniform Th/U ratios (~0.1–0.2), high‐Ti contents (110–190 ppm, corresponding to temperatures of at least 1100 °C), and some (two of 17 mantle analyses) preserve steep heavy rare earth element (HREE) patterns with YbN/GdN = 10–11, with a weak negative Eu anomaly. These signatures are consistent with crystallization from a melt under UHP/ultra‐high‐temperature (UHT) conditions. Some of the bright‐cathodoluminscence (CL) rims preserve Th/U and Ti values characteristic of the zircon mantles, but others show elevated Th/U ratios of ~0.3–0.4 and lower Ti contents (20–40 ppm; only 13 ppm in a rare low‐CL outer rim). As they feature flat HREE patterns and negative Eu anomalies and commonly make embayments and truncate the mantle zoning, we suggest that they have formed through recrystallization in the solid state during exhumation of the rock, when both garnet and plagioclase were stable. The three zircon domains, that is, cores, mantles and rims, yield U–Pb concordia ages of 340.9 ± 1.5, 340.3 ± 1.5 and 341.2 ± 3.4 Ma respectively. When linked to the previously reconstructed P–T path of the rock, the error limits of the zircon mantle and rim ages constrain the exhumation of the rocks from depth of ~140 km (UHP) to ~80 km (HP) to a minimum rate of 1.5 cm yr?1. The zircon cores are heterogeneous in terms of Th/U ratio (below 0.1 but also above 0.2) and REE characteristics, and their εHf values scatter between ?15.7 and +4.8 with similar values for individual domains within a single zircon grain suggesting a very localized control on hafnium isotope composition on a grain scale. The non‐equilibrated εHf values as well as a large range of the Hf‐depleted mantle model ages possibly reflect the presence of a heterogeneous population of old zircon. Consequently, the uniform and young 238U/206Pb ages may represent (near‐)complete resetting of the U–Pb geochronometer during the UHP–UHT event at c. 340 Ma through dissolution–reprecipitation process. In contrast to Hf, the oxygen isotope composition of zircon is homogeneous, ranging between 7.8‰ and 9.6‰ VSMOW, reflecting a source containing upper crustal material and homogenization at UHP–UHT conditions. Our study documents that continental crust was subducted to mantle depths at c. 340 Ma during the Variscan orogeny and was subsequently very rapidly exhumed, implying that the sequence of events was faster than can be resolved by the secondary ion mass spectrometry technique.  相似文献   

13.
研究了人工合成锆石并加入微量元素的实验方法和条件。人工合成锆石是以氧化锆和硅酸锂为原料,以钼酸锂和氧化钼为助熔剂,并加入其他元素如Hf、Lu、Yb、U、Th、Pb等元素,充分混匀后转入带盖铂金坩埚中,在高温马弗炉中连续加热生长形成锆石晶体。利用激光剥蚀系统与电感耦合等离子体质谱技术分析了合成锆石晶体中微量元素含量和Lu-Hf同位素组成,结果表明合成锆石晶体中Lu、Yb、U、Th、Pb等微量元素含量不均一,而Hf的含量和Lu-Hf同位素组成有很好的均一性。  相似文献   

14.
内蒙古克什克腾旗长岭子斜长花岗斑岩位于大兴安岭锡林浩特增生杂岩带内。本文对长岭子斜长花岗斑岩进行了主微量元素地球化学以及锆石U?Pb年代学和Lu?Hf同位素研究。长岭子斜长花岗斑岩锆石206Pb/238U加权平均年龄为(248.1±4.7)Ma,是早三叠世岩浆活动的产物;继承锆石除外,样品中锆石具有正的εHf(t)值(5.78~12.41),二阶段模式年龄TDM2分别为914~488 Ma。长岭子斜长花岗斑岩具有较高的SiO2、Na2O和Al2O3含量以及较低的Fe2O3、MgO和CaO含量,属于偏铝质?过铝质的低钾?钙碱性系列I型花岗岩,富集Rb、K、U、Th、Pb、Sr等大离子亲石元素,亏损Nd、Ta、Ti等高场强元素。同时,斜长花岗斑岩具有高Sr低Y以及高Sr/Y比等特点,具有典型的埃达克质岩石特征,形成于加厚下地壳的部分熔融。综合上述地球化学特征,本文认为长岭子斜长花岗斑岩来源于加厚新生下地壳的部分熔融,表明早三叠世兴蒙地区并非岛弧的环境,而是处于碰撞造山环境,古亚洲洋在该时期已经闭合。  相似文献   

15.
Sediment provenance studies commonly utilize isotopic signatures to resolve detrital mineral sources and routing. However, non-unique ages and geochemical characteristics across geographically distinct crystalline source regions can lead to significant ambiguities in mineral provenance interpretations. Such ambiguity is apparent in southern Australia’s Cenozoic Eucla Basin, which hosts world-class heavy mineral sand resources. Here, new Hf isotope data are provided from four heavy mineral prospects (N = 8, n = 844 [N = samples, n = grains]). Zircon grain shape data are also presented for a suite of detrital Eucla Basin samples (N = 22, n = 35,604) and the basin’s underlying basement, the Coompana Province (N = 13, n = 824). The data are integrated with published detrital and non-detrital primary zircon data to investigate the efficacy of grain shape analysis to better resolve the basin’s mineral provenance. Zircon Hf isotope compositions indicate a primary Mesoproterozoic juvenile source for zircon melts (～1250–1000 Ma, ?2.5 < ?Hf > ～+5) with additional contributions from a range of juvenile to evolved late Archean to Phanerozoic-aged zircon bearing magmas (?28.0 < ?Hf > +11). U–Pb geochronology and Hf isotopes are incapable of differentiating Mesoproterozoic-aged source rocks bounding the region for the majority of heavy mineral deposits analyzed as potential sources express overlapping crystallization ages and similarities in Hf-isotope characteristics. However, distinct zircon grain shapes (i.e., perimeter, major axis and circularity) facilitate improved differentiation across these Mesoproterozoic sources. Filtering of U–Pb age, Hf isotope and shape data implicate the underlying Madura and Coompana provinces as dominant sediment sources for Eucla Basin detritus aged ～1400–1000 Ma. The lack of direct sediment pathways between the underlying basement provinces and placer sediments analyzed demonstrates the significance of zircon reworking from intermediate sedimentary basins in the formation of the economically significant Eucla Basin beach placers. Zircon grain shape represents a cheaply acquired and readily incorporated grain characteristic that can enhance provenance investigations.  相似文献   

16.
Migmatite gneisses are widespread in the Dabie orogen, but their formation ages are poorly constrained. Eight samples of migmatite, including leucosome, melanosome, and banded gneiss, were selected for U–Pb dating and Hf isotope analysis. Most metamorphic zircon occurs as overgrowths around inherited igneous cores or as newly grown grains. Morphological and internal structure features suggest that their growth is associated with partial melting. According to the Hf isotope ratio relationships between metamorphic zircon and inherited cores, three formation mechanisms for metamorphic zircon can be determined, which are dissolution–reprecipitation of pre‐existing zircon, breakdown of Zr‐bearing phase other than zircon in a closed system and crystallization from externally derived Zr‐bearing melt. Four samples contain magmatic zircon cores, yielding upper intercept U–Pb ages of 807 ± 35–768 ± 12 Ma suggesting that the protoliths of the migmatites are Neoproterozoic in age. The migmatite zircon yields weighted mean two‐stage Hf model ages of 2513 ± 97–894 ± 54 Ma, indicating reworking of both juvenile and ancient crustal materials at the time of their protolith formation. The metamorphic zircons give U–Pb ages of 145 ± 2–120 ± 2 Ma. The oldest age indicates that partial melting commenced prior to 145 Ma, which also constrains the onset of extensional tectonism in this region to pre‐145 Ma. The youngest age of 120 Ma was obtained from an undeformed granitic vein, indicating that deformation in this area was complete at this time. Two major episodes of partial melting were dated at 139 ± 1 and 123 ± 1Ma. The first episode of partial melting is obviously older than the timing of post‐collision magmatism, corresponding to regional extension. The second episode of partial melting is coeval with the widespread post‐collision magmatism, indicating the gravitational collapse and delamination of the orogenic lithospheric keel of the Dabie orogen, which were possibly triggered by the uprising of the Cretaceous mid‐Pacific superplume.  相似文献   

17.
SEM back-scattered electron images of zircon separates from a 2.9 Ga granitic dyke from the Acasta Gneiss Complex, Slave Province, reveal primary igneous oscillatory zoning which is transgressively overprinted by irregular alteration domains. Electron microprobe analyses show that altered zircon domains are depleted in Zr and Si relative to unaltered zircon while retaining a constant Zr/Si ratio. SIMS trace element analyses indicate that LREE are preferentially enriched in the altered domains. Altered zircon contains elevated concentrations of Ba (up to 580 ppm), Ca (up to 2% weight of the element) and common Pb (>50 ppb). The presence of LREE, Ca, Ba and common Pb in the zircons is interpreted to be the result of secondary alteration by an aqueous fluid, and not by primary incorporation during crystallization. We propose that the alteration-related elements are located in amorphous zircon domains.  相似文献   

18.
We describe an in situ method for simultaneous measurement of U–Pb–Hf isotopes and trace element compositions of zircons using a quadrupole and multiple-collector inductively-coupled-plasma mass spectrometer (Q-ICP-MS and MC-ICP-MS, respectively) connected to a single excimer laser-ablation system. A laser-generated zircon aerosol was split behind the ablation cell into two transport tubes via a Y-shaped connector and simultaneously introduced into the two mass spectrometers. Hafnium isotopes were measured on the MC-ICP-MS instrument, while U–Pb ages and trace element compositions were determined using the Q-ICP-MS. The precision and accuracy of this method was evaluated using six well-known and widely used zircon standards (91500, Temora-2, GJ-1, Mud Tank, BR266 and Monastery). Analyses were carried out using spot sizes of 32, 44 and 60 μm. For the 44 and 60 μm spot, the resulting U–Pb ages, Hf isotopic and rare earth element (REE) compositions of these six zircons agree with recommended/reported values within 2σ error. The difference in relative standard deviations (RSD) of 206Pb/238U ages between split-flow measurements and those obtained separately on the Q-ICP-MS is within ～ 20% for 91500, Temora-2 and GJ-1, and ～ 60% for Mud Tank (due to its lower U and Pb concentrations). Our method provides a precise approach for determining the U–Pb age and the Hf isotopic and trace element compositions of zircon within a single ablation event. This is in particular important for analysis of zircons that are small or contain complicated zoning patterns. Finally, the REE composition of zircon BR266 is more homogeneous than other zircons and could be a suitable standard by which to benchmark new standards for microprobe analyses of zircons.  相似文献   

19.
《地学前缘(英文版)》2020,11(3):843-853
The combination of U-Pb and Lu-Hf compositions measured in zircon crystals is a remarkably powerful isotopic couplet that provides measures on both the timing of mineral growth and the radiogenic enrichment of the source from which the zircon grew.The U-Pb age documents the timing of zircon crystallization/recrystallization and Hf isotopes inform on the degree to which the host melt was derived from a radiogenic reservoir(e.g.depleted mantle) versus an unradiogenic reservoir(e.g.ancient continental crust),or some mixture of these sources.The ease of generating large quantities of zircon U-Pb and Lu-Hf data has been in large part facilitated by instrument advances.However,the dramatic increase in time constrained zircon Lu-Hf analyses in the Earth science community has brought to the fore the importance of careful data collection and reduction workflows,onto which robust geological interpretations may be based.In this work,we discuss the fundamentals of Lu-Hf isotopes in zircon,which then allows us to provide a robust,accessible,methodology for the assessment of data quality.Additionally,we discuss some novel techniques for:data visualization—that facilitates better transparency of data interpretation;integration of geographic information—that may reveal spatial trends where temporal trends were only apparent before;and some novel statistical evaluation tools—that may provide more rigorous interand intra-sample comparisons.  相似文献   

20.
Zircon has been synthesized from a large number of mineral salts and also from one organic compound of zirconium. Its crystallization requires an acid reactive environment.The obtained crystals have been studied morphologically and the crystallographic forms obtained are linked to the presence of specific ions.The study of substitutions in the zircon network shows that hydro-zircon αZr(SiO4)1?x(OH)4x will form only when fluorine is present. Other varieties of the α and β phases ZrSiO4 have been obtained, substituting Hf, U, for Zr, and Ge for Si and an immiscible α phase ThSiO4.Germanium enters the zircon network only at low temperature. Uranium and Hf, but not Th, can substitute for Zr in zircon.  相似文献   

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