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 mineral zircon is extremely variable both in terms of external morphology and internal textures. These features reflect the geologic history of the mineral, especially the relevant episode(s) of magmatic or metamorphic crystallization (and recrystallization), strain imposed both by external forces and by internal volume expansion caused by metamictization, and chemical alteration. The paper presents a selection of both the most typical, but also of the less common, features seen in zircon, categorized according to the different geological processes responsible for their formation. The atlas is intended as a general guide for the interpretation of zircon characteristics, and of related isotopic data.

Zircon has become one of the most widely used minerals for the extraction of information on the prehistory and genesis of magmatic, metamorphic and sedimentary rocks. Much of the geological usefulness of zircon stems from its suitability as a geochronometer based on the decay of U (and Th) to Pb, but in addition it is also the major host of the radiogenic isotopic tracer Hf, and it is used to determine oxygen isotopic compositions and REE and other trace element abundances, all of which yield useful clues concerning the history of the host rock, and in some case, the parent rock in which the precursor zircon crystallized.

One of the major advantages of zircon is its ability to survive magmatic, metamorphic and erosional processes that destroy most other common minerals. Zircon-forming events tend to be preserved as distinct structural entities on a pre-existing zircon grain. Because of this ability, quite commonly zircon consists of distinct segments, each preserving a particular period of zircon-formation (or consumption). A long experience and modern instrumentation and techniques have provided the “zircon community” the means to image and interpret preserved textures, and hence to decipher the history and evolution of a rock. One …

Atlas of Zircon Textures

Assembly, configuration, and break-up history of Rodinia: A synthesis

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

Corundums from basalt fields, particularly in Australia and Asia, include a dominant blue-green-yellow zoned “magmatic” suite (BGY suite) and subsidiary vari-coloured “metamorphic” suites. The BGY corundums have distinctive trace element contents (up to 0.04 wt% Ga2O3 and low Cr/Ga and Ti/Ga ratios <1). Different melt origins for BGY corundums are considered here from their inclusion and intergrowth mineralogy, petrologic associations and tectonic setting. Analysed primary inclusion minerals (over 100 inclusions) cover typical feldspars, zircon and Nb-Ta oxides and also include hercynite-magnetite, gahnospinel, rutile-ilmenite solid solution, calcic plagioclase, Ni-rich pyrrhotite, thorite and low-Si and Fe-rich glassy inclusions. This widens a previous inclusion survey; New England, East Australia corundums contain the most diverse inclusion suite known from basalt fields (20 phases). Zircon inclusion, intergrowth and megacryst rare earth element data show similar patterns, except for Eu which shows variable depletion. Temperature estimates from magnetite exsolution, feldspar compositions and fluid inclusion homogenization suggest that some corundums crystallized between 685–900 °C. Overlap of inclusion Nb, Ta oxide compositions with new comparative data from niobium-yttrium-fluorine enriched granitic pegmatites favour a silicate melt origin for the corundums. The feasibility of crystallizing corundum from low-volume initial melting of amphibole-bearing mantle assemblages was tested using the MELTS program on amphibole-pyroxenite xenolith chemistry from basalts. Corundum appears in the calculations at 720–880 °C and 0.7–1.1 GPa with residual feldspathic assemblages that match mineral compositions found in corundums and their related xenoliths. A model that generates melts from amphibole-bearing lithospheric mantle during magmatic plume activity is proposed for BGY corundum formation.

Models of corundum origin from alkali basaltic terrains: a reappraisal

Minor and trace element analysis of natural zircon (ZrSiO4) by SIMS and laser ablation ICPMS : A consideration and comparison of two broadly competitive techniques

Zircons from anatectic melts of the country rocks of three Proterozoic mafic–ultramafic intrusions from the Sveconorwegian Province in SW Sweden were microanalyzed for U–Th–Pb and rare earth elements. Melting and interaction of the wall rocks with the intrusions gave rise to new magmas that crystallized zircon as new grains and overgrowths on xenocrysts. The ages of the intrusions can be determined by dating this newly crystallized zircon. The method is applied to three intrusions that present different degrees of complexity, related to age differences between intrusion and country rocks, and the effects of post-intrusive metamorphism. By careful study of cathodoluminescent images and selection of ion probe spots in zircon grains, we show that this approach is a powerful tool for obtaining accurate and precise ages. In the contact melts around the 916 ± 11 Ma Hakefjorden Complex, Pb-loss occurred in some U-rich parts of xenocrystic zircon due to the heat from the intrusion. In back-veins of the 1624 ± 6 Ma Olstorp intrusion we succeeded in geochemically distinguishing new magmatic from xenocrystic zircon despite small age differences. At Boras the mafic intrusion mixed with country rock granite to form a tonalite in which new zircon grew at 1674 ± 8 Ma. Reworking of zircon occurred during 930+33/–34 Ma upper amphibolite facies Sveconorwegian metamorphism. Pb-loss was the result of re-equilibration with metamorphic fluids. REE-profiles show consistent differences between xenocrystic, magmatic, and metamorphic zircon in all cases. They typically differ in Lu/LaN, Ce/Ce*, and Eu/Eu*, and igneous zircon with marked positive Ce/Ce* and negative Eu/Eu* lost its anomalies during metamorphism.

Dating mafic-ultramafic intrusions by ion-microprobing contact-melt zircon: examples from SW Sweden

Epidote group minerals are common in metamorphosed mafic to intermediate igneous rocks, quartzofeldspathic sediments and calc-alumina silicate (marl) rocks of higher grade zeolite to medium grade amphibolite facies of low–medium pressure contact and regional metamorphic terranes (i.e., pressure and temperature conditions below the calcite-to-aragonite transition). Within any one rock, epidote composition in terms of Fe3+/(Fe3+ + Al) can be variable, but in general, is limited by whole-rock composition, such that epidote group minerals in metabasite lithologies are more Fe-rich than those in marls that tend to be more Al-rich and typically include zoisite. Because of their wide range of P - T stability, epidote group minerals of variable composition may form in a single rock during several stages of metamorphic re-equilibration. Slow rates of intra-crystalline Fe3+-Al exchange, especially at low temperatures, preserve complex zonation patterns in individual grains that can serve as a “tape-recorder” providing evidence for continuous or discontinuous prograde and retrograde reactions and the P - T -fluid-redox conditions of metamorphism. Thus, relic lower grade epidote (typically Fe-rich) often form cores over which new (typically less Fe-rich) higher grade epidote rims form. In such a case, the boundary between the two generations of epidote may be sharp or gradational depending on the temperature history of the rock and Fe3+-Al diffusivity. Often compositional differences are blurred across the boundary. In addition to zoning is the spread of individual epidote grain compositions within a rock (even on a thin-section scale). This is related to variation in the composition of coexisting phases or reactants (e.g., quartz; Ca-Al silicates such as plagioclase, margarite, lawsonite; mafic silicates such as chlorite, pumpellyite, amphiboles; other Ca-Fe3+ silicates such as prehnite, andraditic garnet; carbonates; Fe-oxides; relict volcanic glass), which serve as compositional micro-domains in which epidote may form. …

Paul W.O. Hoskin

Papers

Models of corundum origin from alkali basaltic terrains: a reappraisal

Minor and trace element analysis of natural zircon (ZrSiO4) by SIMS and laser ablation ICPMS : A consideration and comparison of two broadly competitive techniques

Dating mafic-ultramafic intrusions by ion-microprobing contact-melt zircon: examples from SW Sweden

Epidote Group Minerals in Low–Medium Pressure Metamorphic Terranes

Raman spectral shift in the isomorphous series (Zr1-xHfx)SiO4