The application of laser ablation-inductively coupled plasma-mass spectrometry to in situ U–Pb zircon geochronology

Zircon is the main mineral in the majority of igneous and metamorphic rocks with Zr as an essential structural constituent. It is a host for significant fractions of the whole-rock abundance of U, Th, Hf, and the REE (Sawka 1988, Bea 1996, O’Hara et al. 2001). These elements are important geochemically as process indicators or parent isotopes for age determination. The importance of zircon in crustal evolution studies is underscored by its predominant use in U-Th-Pb geochronology and investigations of the temporal evolution of both the crust and lithospheric mantle. In the past decade an increasing interest in the composition of zircon, trace-elements in particular, has been motivated by the effort to better constrain in situ microprobe-acquired isotopic ages. Electron-beam compositional imaging and isotope-ratio measurement by in situ beam techniques—and the micrometer-scale spatial resolution that is possible—has revealed in many cases that single zircon crystals contain a record of multiple geologic events. Such events can either be zircon-consuming, alteration, or zircon-forming and may be separated in time by millions or billions of years. In many cases, calculated zircon isotopic ages do not coincide with ages of geologic events determined from other minerals or from whole-rock analysis. To interpret the geologic validity and significance of multiple ages, and ages unsupported by independent analysis of other isotopic systems, has been the impetus for most past investigations of zircon composition. Some recent compositional investigations of zircon have not been directly related to geochronology, but to the ability of zircon to influence or record petrogenetic processes in igneous and metamorphic systems.

Sedimentary rocks may also contain a significant fraction of zircon. Although authigenic zircon has been reported (Saxena 1966, Baruah et al. 1995, Hower et al. 1999), it appears to be very rare and may in fact be related to …

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The Composition of Zircon and Igneous and Metamorphic Petrogenesis

Plesovice zircon : A new natural reference material for U-Pb and Hf isotopic microanalysis

The Hf isotope composition of cratonic mantle: LAM-MC-ICPMS analysis of zircon megacrysts in kimberlites

We present the first finding of continental crust-derived Precambrian zircons in garnet/spinel pyroxenite veins within mantle xenoliths carried by the Neogene Hannuoba basalt in the central zone of the North China Craton (NCC). Petrological and geochemical features indicate that these mantle-derived composite xenoliths were formed by silicic melt^lherzolite interaction. The Precambrian zircon ages can be classified into three age groups of 2·4^2·5 Ga, 1·6^2·2 Ga and 0·6^1·2 Ga, coinciding with major geological events in the NCC. These Precambrian zircons fall in the field of continental granitoid rocks in plots of U/Yb vs Hf and Y. Their igneous-type REE patterns and metamorphic zircon type CL images indicate that they were not crystallized during melt^peridotite interaction and subsequent high-pressure metamorphism.The 2·5 Ga zircons have positive eHf(t) values (2·9^10·6), whereas the younger Precambrian zircons are dominated by negative eHf(t) values, indicating an ancient continental crustal origin.These observations suggest that the Precambrian zircons were xenocrysts that survived melting of recycled continental crustal rocks and were then injected with silicate melt into the host peridotite. In addition to the Precambrian zircons, igneous zircons of 315 3 Ma (2 ), 80^170 Ma and 48^64 Ma were separated from the garnet/spinel pyroxenite veins; these provide evidence for lower continental crust and oceanic crust recycling-induced multi-episodic melt^peridotite interactions in the central zone of the NCC. The combination of the positive eHf(t) values (2·91^24·6) of the 315 Ma zircons with the rare occurrence of 302^324 Ma subduction-related diorite^granite plutons in the northern margin of the NCC implies that the 315 Ma igneous zircons might record melt^peridotite interactions in the lithospheric mantle induced by Palaeo-Asian oceanic crust subduction. Igneous zircons of age 80^170 Ma generally coexist with the Precambrian metamorphic zircons and have lower Ce/Yb and Th/U ratios, higher U/Yb ratios and greater negative Eu anomalies.The eHf(t) values of these zircons vary greatly from ^47·6 to 24·6.The 170^110 Ma zircons are generally characterized by negative eHf(t) values, whereas the 110^100 Ma zircons have positive eHf(t) values.These observations suggest that melt^peridotite interactions at 80^170 Ma were induced by partial melting of recycled continental crust. The 48^64 Ma igneous zircons are characterized by negligible Ce anomalies, unusually high REE, U and Th contents, and positive eHf(t) values.These features imply that the melt^peridotite interactions at 48^64 Ma could be associated with a depleted mantle-derived carbonate melt or fluid.

Continental and Oceanic Crust Recycling-induced Melt^Peridotite Interactions in the Trans-North China Orogen: U^Pb Dating, Hf Isotopes and Trace Elements in Zircons from Mantle Xenoliths

We report here the results of a study to develop natural zircon geochemical standards for calibrating the U-(Th)-Pb geochronometer and Hf isotopic analyses. Additional data were also collected for the major, minor and trace element contents of the three selected sample sets. A total of five large zircon grains (masses between 0.5 and 238 g) were selected for this study, representing three different suites of zircons with ages of 1065 Ma, 2.5 Ma and 0.9 Ma. Geochemical laboratories can obtain these materials by contacting Geostandards Newsletter.

Three natural zircon standards for u‐th‐pb, lu‐hf, trace element and ree analyses

A unique laboratory experimental setup for single-crystal X-ray diffraction under electric field

The ability of a wide span of characterization and analytical tools to provide reliable, quantitative data for monitoring the efficiency of photocatalysis in the mineralization of calibrated polystyrene nanobeads was studied. Both slurry and immobilized reaction modes were compared, and polystyrene nanoparticles of different characteristic sizes were used as model compounds for developing a suited methodological approach. We demonstrated that tests in the immobilized mode showed an unequivocal advantage over the slurry mode and in consequence should be preferred to get rid of the restrictive presence of the nanoparticulate photocatalyst within the samples to be analysed. At best, the results in the slurry mode revealed the existence of a photocatalytic activity towards polystyrene nanobeads, with no capacity of reliable quantification. Direct imaging or indirect light-scattering characterization giving a direct access to the size of the nanoplastic particles cannot provide fully relevant data, as the polystyrene substrate was reported to lose its nanobead morphology during the photocatalytic attack, in parts or entirely, with the simultaneous release to the water of polystyrene macromolecules. Py-GC/MS allowed the polystyrene concentration to be followed with time, but with no access to the concentration of polystyrene nanoparticles. TOC analysis remained the most suited and reliable technique to monitor and quantify the mineralization of polystyrene nanoplastics by photocatalysis. UV-Vis spectrophotometry was reported to be a fast, non-destructive alternative technique to TOC analysis in the specific case of polystyrene. 

P. Allé

Papers

Three natural zircon standards for u‐th‐pb, lu‐hf, trace element and ree analyses

A unique laboratory experimental setup for single-crystal X-ray diffraction under electric field

Photocatalytic Degradation of Polystyrene Nanoplastics in Water. A Methodological Study