In situ LA-(MC)-ICP-MS trace element and Nd isotopic compositions and genesis of polygenetic titanite from the Baogutu reduced porphyry Cu deposit, Western Junggar, NW China

2015 ◽  
Vol 65 ◽  
pp. 940-954 ◽  
Author(s):  
MingJian Cao ◽  
KeZhang Qin ◽  
GuangMing Li ◽  
Noreen J. Evans ◽  
LuYing Jin
2022 ◽  
Author(s):  
Jérémie Soldner ◽  
Yingde Jiang ◽  
et al.

Table S1: U-Pb LA-ICP-MS data for zircons from granulite and amphibolite. Table S2: U-Pb LA-ICP-MS data for zircons from metapelite and metapsammite. Table S3: Zircon trace-element compositions from granulite and amphibolite. Table S4: Hf isotopic compositions for zircons from granulite and amphibolite.


2022 ◽  
Author(s):  
Jérémie Soldner ◽  
Yingde Jiang ◽  
et al.

Table S1: U-Pb LA-ICP-MS data for zircons from granulite and amphibolite. Table S2: U-Pb LA-ICP-MS data for zircons from metapelite and metapsammite. Table S3: Zircon trace-element compositions from granulite and amphibolite. Table S4: Hf isotopic compositions for zircons from granulite and amphibolite.


Geochronology ◽  
2020 ◽  
Vol 2 (2) ◽  
pp. 209-230 ◽  
Author(s):  
Simon J. E. Large ◽  
Jörn-Frederik Wotzlaw ◽  
Marcel Guillong ◽  
Albrecht von Quadt ◽  
Christoph A. Heinrich

Abstract. Understanding the formation of economically important porphyry Cu–Au deposits requires knowledge of the magmatic-to-hydrothermal processes that act within the much larger magmatic system and the timescales on which they occur. We apply high-precision zircon geochronology (chemical abrasion–isotope dilution–thermal ionisation mass spectrometry; CA–ID–TIMS) and spatially resolved zircon geochemistry (laser ablation inductively coupled plasma mass spectrometry; LA-ICP-MS) to constrain the magmatic evolution of the underlying magma reservoir at the Pliocene Batu Hijau porphyry Cu–Au deposit. We then use this extensive dataset to assess the accuracy and precision of different U–Pb dating methods of the same zircon crystals. Emplacement of the oldest pre- to syn-ore tonalite (3.736±0.023 Ma) and the youngest tonalite porphyry to cross-cut economic Cu–Au mineralisation (3.646±0.022 Ma) is determined by the youngest zircon grain from each sample, which constrains the duration of metal precipitation to fewer than 90±32 kyr. Overlapping spectra of single zircon crystallisation ages and their trace element distributions from the pre-, syn and post-ore tonalite porphyries reveal protracted zircon crystallisation together with apatite and plagioclase within the same magma reservoir over >300 kyr. The presented petrochronological data constrain a protracted early >200 kyr interval of melt differentiation and cooling within a large heterogeneous magma reservoir, followed by magma storage in a highly crystalline state and chemical and thermal stability over several tens of thousands of years during which fluid expulsion formed the ore deposit. Irregular trace element systematics suggest magma recharge or underplating during this final short time interval. The comparison of high-precision CA–ID–TIMS results with in situ LA-ICP-MS and a sensitive high-resolution ion microprobe (SHRIMP) U–Pb geochronology data from the same zircon grains allows a comparison of the applicability of each technique as a tool to constrain dates and rates on different geological timescales. All techniques provide accurate dates but with different precision. Highly precise dates derived by the calculation of the weighted mean and standard error of the mean of the zircon dates obtained by in situ techniques can lead to ages of unclear geological significance that are older than the maximum ages of emplacement given by the CA–ID–TIMS ages of the youngest zircons in each sample. This lack of accuracy of the weighted means is due to the protracted nature of zircon crystallisation in upper crustal magma reservoirs, suggesting that standard errors should not be used as a means to describe the uncertainty in those circumstances. We conclude from this and similar published studies that the succession of magma and fluid pulses forming a single porphyry deposit and similarly rapid geological events are too fast to be reliably resolved by in situ U–Pb geochronology and that assessing the tempo of ore formation requires CA–ID–TIMS geochronology.


2020 ◽  
Author(s):  
Veronica Peverelli ◽  
Tanya Ewing ◽  
Daniela Rubatto ◽  
Martin Wille ◽  
Alfons Berger ◽  
...  

Abstract. Monoclinic epidote is a low-µ (µ = 283U / 204Pb) mineral occurring in a variety of geological environments, participating in many metamorphic reactions and stable throughout a wide range of pressure–temperature conditions. Despite containing fair amounts of U, its use as a U–Pb geochronometer has been hindered by the commonly high contents of initial Pb with isotopic compositions that cannot be assumed a priori. We present U–Pb geochronology of hydrothermal-vein epidote spanning a wide range of Pb (3.9–190 µg g−1), Th (0.009–38 µg g−1) and U (2.6–530 µg g−1) contents and with µ values between 7–510 from the Albula area (eastern Swiss Alps), from the Grimsel area (central Swiss Alps) and from the Heyuan fault (Guangdong province, China). The investigated epidote samples show appreciable fractions of initial Pb that vary to different extents. A protocol has been developed for in situ U–Pb dating of epidote by spot-analysis laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS) with a magmatic allanite as primary reference material. The suitability of the protocol and the reliability of the measured isotopic ratios have been ascertained by independent measurements of 238U / 206Pb and 207Pb / 206Pb ratios respectively by quadrupole and multicollector ICP–MS applied to epidote micro-separates digested and diluted in acids. For age calculation, we used the Tera–Wasserburg (207Pb / 206Pb–238U / 206Pb) diagram, which does not require corrections for initial Pb and provides the initial 207Pb / 206Pb ratio if all intra-sample analyses are co-genetic. Petrographic and microstructural data indicate that the calculated ages date the crystallization of vein epidote from a hydrothermal fluid and that the U–Pb system was not reset to younger ages by later events. Vein epidote from the Albula area formed in the Paleocene (62.7 ± 3.0 Ma) and is related to Alpine greenschist-facies metamorphism. The Miocene (19.1 ± 4.0 Ma and 16.9 ± 3.7 Ma) epidote veins from the Grimsel area formed during the Handegg phase (22–17 Ma) of the Alpine evolution of the Aar Massif. Identical initial 207Pb / 206Pb ratios reveal homogeneity in Pb isotopic compositions of the fluid across ca. 200 m. Vein epidote from the Heyuan fault is Cretaceous in age (108.1 ± 8.4 Ma) and formed during the early movements of the fault. In situ U–Pb analyses of epidote returned reliable ages of otherwise undatable epidote-quartz veins. The Tera–Wasserburg approach has proven pivotal for in situ U–Pb dating of epidote and the decisive aspect for low age uncertainties is the variability in intra-sample initial Pb fractions.


2020 ◽  
Vol 58 (3) ◽  
pp. 293-311 ◽  
Author(s):  
Zeinab Azadbakht ◽  
David R. Lentz

ABSTRACT Biotite grains from 22 felsic intrusions in New Brunswick were mapped in situ using a laser ablation-inductively coupled plasma-mass spectrometer (LA-ICP-MS). We investigated the extent to which biotite can retain its magmatic zoning patterns and, where zoning does exist, how it can be used to elucidate early to late stage, syn-magmatic to post-crystallization processes. Although the major element and halogen contents of the examined biotite phenocrysts are homogeneous, two-thirds of the grains display trace-element zoning for Ba, Rb, and Cs. The results also indicated that zoning is better retained in larger grains (i.e., > 500 × 500 μm) with minimal alteration and mineral inclusions. An exceptionally well-zoned Li-rich siderophyllite from the Pleasant Ridge topaz granite in southwestern New Brunswick shows Ti, Ta, Sn, W, Cs, Rb, and V (without Li or Ba) zoning. Cesium values increase from 200 to 1400 ppm from core to rim. Conversely, Sn and W values decrease toward the rim (50 to 10 and 100 to 10 ppm, respectively). Tantalum and Ti values show fewer variations but drop abruptly close to the rim of the grain (100 to 20 and 2000 to 500 ppm, respectively). These observations may indicate crystallization of mineral phases with high partition coefficients for these highly incompatible elements (except Ti) (e.g., cassiterite and rutile) followed by fractionation of a fluid phase at a later stage of magma crystallization. The preservation of zoning may indicate rapid cooling post-crystallization of the parent magma.


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