Abstract
Zircons gneisses and migmatites collected from the Antarctic Peninsula have different core–rim hafnium isotope ratio relationships depending on whether evidence for zircon dissolution is present or absent. Two samples contain inherited zircon that is partially dissolved. In these samples, the 176Hf/177Hf rations of the inherited zircon and new magmatic zircon rims are, on average, indistinguishable and consistent with in situ melting. In such cases the hafnium isotopic composition of the melt was probably strongly influenced by the dissolved zircon component at the source. Variation in 176Hf/177Hf within the magmatic zircon rims from grain to grain suggests that Hf isotopes were only partially homogenized during melt migration; alternatively, zircon growth may have taken place within small volumes of partial melt. Other samples do not preserve textural evidence for zircon dissolution during melt generation; in these samples the 176Hf/177Hf values of the inherited zircon and new magmatic zircon rims are different. The zircon rims apparently suggest a source of less evolved hafnium than that contained within the inherited zircon. Whether this relates to a separate juvenile source or, alternatively, is derived from minerals other than zircon at the source, cannot be resolved. Inherited zircon, irrespective of age, has been strongly influenced by the reworking of a juvenile Late Mesoproterozoic source, suggesting that such crust underlies the Antarctic Peninsula. Our results therefore suggest that Hf isotope analyses provide great potential for future studies investigating the source and processes involved in the generation of crustal melts.
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Introduction
For most crustal processes zircon grains behave in a refractory way, which makes them unparalleled recorders of the source region history of both magmatic and sedimentary rocks. Inherited zircon grains from crust-derived granitoid and migmatitic rocks are commonly studied in order to characterize their source region (e.g., Clemens 2003). Given their refractory nature, zircon grains can be entrained in, and carried along with, melt during crustal anatexis (Watson and Harrison 1983; Williams and Claesson 1987; Paterson et al. 1992; Clemens 2003). The two most successfully applied techniques in studying the provenance of such inherited zircons involve determining their U–Pb age distribution (Pidgeon and Compston 1992; Williams 1995, 2001; Maas et al. 2001; Tikhomirova 2002; Zeck and Williams 2002; Scherstèn et al. 2004) or their REE chemistry (Hoskin and Schalteggar 2003; Whitehouse and Kamber 2003).
Like the U–Pb system, the Lu–Hf system is refractory in zircon during crustal melting and Hf isotope inheritance has commonly been recognized (e.g., Smith et al. 1987; Corfu and Noble 1992). With the refinement of in situ analysis techniques (Kinny et al. 1991; Thirlwall and Walder 1995) a more rigorous evaluation of the Hf isotope character in complex zircon grains is now possible. In situ measurement of Hf isotopes in zircon has been successfully applied to studies of ancient (Andersen et al. 2002; Knudsen et al. 2001; Veevers et al. 2005) and modern sedimentary zircon provenance (Griffin et al. 2004), metamorphic gneiss terranes (Halpin et al. 2005) and aspects of igneous petrogenesis (Andersen and Griffin 2004; Griffin et al. 2002). However, the study of the zircon xenocrysts within igneous rocks is largely dedicated to restitic lower crustal material and zircon megacrysts brought to the surface as xenocrysts and xenoliths within kimberlites (Griffin et al. 2000; Zheng et al. 2004). In this study, we describe the growth history, U–Pb age and Hf isotope signature of complex zircons within mid-crustal migmatites and granitic gneisses from four separate localities along the Antarctic Peninsula (Fig. 1). In addition we compare zircon grains from a leucogranite with its proposed source rock. From these analyses we evaluate the benefits of measuring Hf isotopes in xenocrystic zircon in understanding the melted source rocks.
Geology
Traditionally, the Antarctic Peninsula is modeled as having developed as an Andean-style margin from the Mesozoic through the Cenozoic (Suárez 1976; Leat et al. 1995), although more recent work has identified suspect terranes making up the western part of the Peninsula (Vaughan and Storey 2000). Intermittent magmatism, deformation and metamorphism related to subduction beneath the Antarctic Peninsula, affected Mesozoic and pre-Mesozoic basement (e.g., Millar et al. 2002).
Events such as continental breakup (Storey 1991; Storey et al. 1988), extension (Vaughan and Millar 1996; Vaughan et al. 1997) and compression (Vaughan et al. 2002) that possibly involved terrane accretion (Vaughan and Storey 2000) during the development of the Antarctic Peninsula sector of the Gondwana margin, have exposed interior portions of arc basement and continental margin basement in some areas.
Separate episodes of metamorphism and anatexis affected different parts of the Antarctic Peninsula in the Carboniferous, Permian, Middle and Late Triassic (Millar et al. 2002). The Silurian, Late Triassic igneous activity and metamorphism is often viewed as a response to the initiation of subduction along the Antarctic Peninsula (e.g., Leat et al. 1995); however, given the dominantly S-type nature the granitoids, Millar et al. (2002) suggested that this may not be the case. The conditions of metamorphism are poorly understood. However, in northwest Palmer Land (Fig. 1), geothermobarometry from migmatized paragneisses suggests conditions ranging between 800°C at 5–6 kbar and 600°C at 2 kbar (Piercy and Harrison 1991). Piercy and Harrison (1991) proposed that magmatic heating in an arc caused metamorphism, rather than burial and compaction as in a mountain belt. The rocks recording higher pressures and temperatures of metamorphism therefore represent the exposure of deeper crustal levels from within the arc.
Analytical methods
U–Pb zircon analyses were performed by sensitive high-resolution ion-microprobe (SHRIMP) at the Australian National University, Canberra. The analytical procedure follows that reported by Williams (1998) and references therein, and is only briefly outlined below.
Zircons were separated, using standard heavy liquid and magnetic techniques, from approximately 1 to 2 kg of rock crushed to < 300 μm. Following handpicking, the zircons were mounted in epoxy along with a few grains of the 1,099 Ma AS3 zircon standard (Schmitz et al. 2003), and polished to expose the centers of the grains, before optical and Cathodoluminescence (CL) imaging. The mount was cleaned and coated with an 80 μm layer of gold and then introduced into the ion-microprobe. Analysis was carried out using a focused primary O2-beam, and secondary ion intensities were measured with an ion-counting detector. A beam diameter of ∼30 μm was used, which resulted in pits 1–2 μm deep. Pb/U ratios were calibrated against the zircon standard using the measured UO/U ratios. The 204Pb signal for each analysis assessed the amount of common Pb. Common Pb was not corrected for and is assumed to be from surface contamination with a composition of present day values for terrestrial Pb. Concordia ages quoted in the text have been calculated using ISOPLOT version 3.1 (Ludwig 1999) using the decay constants recommended by Steiger and Jäger (1977) and are quoted throughout at the 2σ level.
After SHRIMP analysis, the gold coating was removed using tissue and alcohol and the mounts were cleaned before Hf analysis. Hf analyses were performed using a 266 nm Merchantek Nd:YAG laser attached to a VG Axiom multi-collector inductively coupled mass spectrometer at the NERC Isotope Geosciences Laboratory, UK. Analyses were carried out, where possible, on top of the original ion-microprobe-generated pit, so that Hf analysis could be paired with different stages of zircon growth. Where it was not possible to do so, CL images were used to locate areas of zircon likely to have the same age. The overall analytical approach followed closely that of Horstwood et al. (2003), but with the following modifications for Hf analysis of zircon.
Ablations of 50 μm diameter pits were achieved using a laser beam with a 10 Hz repetition rate and energy of ca. 40 J cm−2. Where possible, 75 ratios of 1 s integrations were collected. However, many analyses were targeted at small inherited cores and thin zircon rims, and suitable material permitted only approximately 20–30 s of data collection. Each analysis typically resulted in a pit depth of approximately 50 μm. A Ta monitor solution was aspirated via a Cetac Technologies Aridus desolvating nebuliser into a modified laser cell (Horstwood et al. 2003), so that the instrument settings and gas flows for both the aspirated and ablated material could be optimized. Additionally, by centering on the stable, aspirated Ta signal, rather than the unstable laser-ablated Hf signal, the centering routine is accurate and the amount of zircon available for Hf data acquisition is maximized.
Masses 172, 173, 175, 176, 177, 178, 179, 180 and 181 were collected in static collection mode in Faraday cups, with mass 177 occupying the axial collector. Data were corrected for mass bias using an exponential law and a value of 0.7325 for 179Hf/177Hf. Laser induced isotope fractionation during ablation was not evident. Such fractionation was monitored using the 178Hf/177Hf and 180Hf/177Hf stable isotope ratios, which for the 91,500 zircon standard yielded values of 1.88664 ± 42 (2 SD, n = 41) and 1.46710 ± 23 (2 SD, n = 41), respectively. JMC 475 standard solution was run during of analyses and yielded 0.282133 ± 24 (2 SD, n = 27). Subsequently, our unknown analyses were normalized relative to the accepted value for JMC 475 of 0.28216 (Nowell et al. 1998). This low value is within error of the laboratory 8 month average for the JMC 475 standard solution, which yields a value of 0.282146 ± 74 ppm, and may relate to aspiration via the Cetac Technologies Aridus desolvating nebuliser. A total of 41 analyses of the 91,500 zircon standard (with an accepted 176Hf/177Hf of ∼0.28230; Wiedenbeck et al. 1995; Woodhead et al. 2004), were acquired intermittently during the analytical session, which after reduction and normalization to the JMC475 standard, gave 176Hf/177Hf = 0.282310 ± 66 (± 2 SD, n = 41). Data were reduced off-line in a time-resolved fashion so that any changes in 176Hf/177Hf that may correspond to ablation though different growth zones (or occasionally through the grain into the epoxy mount) can be identified.
Corrections for the Ta aspirated into the laser cell were performed by way of a simple reverse mass-biased corrected (using 179Hf/177Hf) subtraction of 180Ta based on the measured 181Ta peak. Ta-doped JMC475 standard gave 0.282130 ± 30 (2 SD, n = 12), indistinguishable from the results obtained from undoped JMC475 (see above). 180Ta typically resulted in 3,000 counts s−1, approximately 0.005% of the 180 beam, making the 180Ta interference insignificant.
Correction for the significant 176Yb and 176Lu interferences on the 176Hf peak following the method outlined by Thirlwall and Walder (1995) and Nowell and Parrish (2001), which has been successfully adopted in a variety of Hf laser-ablation studies of zircon (e.g. Griffin et al. 2000; Andersen et al. 2002; Griffin et al. 2002; Zheng et al. 2004; Veevers et al. 2005). Mass bias corrections for Yb were assumed to be similar to that for the measured 179Hf/177Hf and although Chu et al. (2002) demonstrated the mass bias behavior of Hf and Yb were subtly different, they concluded that the assumption was appropriate for such mass bias correction. For our analyses, Yb was corrected for 176Yb/173Yb = 0.795238. Yb-doped JMC475 solutions with Yb/Hf of 0.05 and 0.1 yielded 0.282126 ± 26 (2 SD, n = 11) and 0.282132 ± 16 (2 SD, n = 10), respectively, within error of the undoped and Ta-doped JMC 475 solutions (see above). The same protocol was followed to establish a Lu correction factor of 176Lu/175Lu of 0.026522. Lu correction proved insignificant given the small Lu concentrations of the analyzed zircons. However, ɛHf and t DM model ages (Table 2) were always calculated on the Lu uncorrected ratios.
Our Yb corrections were deemed appropriate on three counts. Firstly, the Yb-doped JMC475 solution gave 176Hf/177Hf indistinguishable to those analyses without doping. Secondly, laser ablation analyses of the 91500 zircon standard gave 176Hf/177Hf within error of the currently accepted values for the standard. Thirdly, time-resolved analysis allows variations in Yb concentration to be identified as the sample is ablated. During several analyses three-fold changes in Yb concentration did not result in any change in the Yb-corrected 176Hf/177Hf (Fig. 2).
Field relations, petrography and geochronology
Adie Inlet gneiss, R.349.2
The Adie Inlet gneiss (Pankhurst 1983) forms part of a wider area of intermittent exposure of mixed lithology that stretches from Adie Inlet to Gulliver Nunatak on the Eastern Coast of Graham Land (Fig. 1). Early Jurassic volcanics, with numerous gneissic xenoliths, structurally overlie the gneiss exposures (Thomson and Pankhurst 1983). The analyzed sample is a sub-rounded, coarse-grained enclave, composed of porphyroblastic K-feldspar within a K-feldspar–plagioclase–quartz–biotite–muscovite matrix, hosted in a leucogranite gneiss matrix. It may represent restite within the gneiss. Both gneiss and enclave are migmatized. Zircons are variously elongate and form multifaceted crystals. CL images reveal that most grains comprise a core, surrounded by a thin 20 μm overgrowth (Fig. 3a), such that the size and shape of the core determines the size and shape of the zircon. Overgrowths are dark in CL and sometimes exhibit fine-scale growth zonation. Cores vary from angular and broken to more commonly rounded or sub-rounded and are interpreted to be inherited. The CL of the inherited cores is highly variable but most grains have growth zoning patterns that are terminated by the later relatively non-luminescent overgrowth. A few grains show an irregular margin between core and rim (e.g. grain 21, Fig. 3a) but in the great majority of grains, the boundary between core and rim is regular and sharp.
U–Pb geochronology, previously performed by Millar et al. (2002) using SHRIMP, of the inherited zircon cores gave age clusters at ca. 500–550 Ma and 1,000–1,050 Ma (Fig. 4a). The ages of the inherited zircons are similar in age to detrital zircon populations from nearby sediments (BAS unpublished data), and suggest that the enclave has a sedimentary protolith. The non-luminescent rims gave a Late Permian age of 258 ± 3 Ma (Millar et al. 2002) confirming a Permian age for migmatization, previously determined by Rb–Sr and K–Ar biotite mineral ages (Rex 1976; Pankhurst 1983). However, it must be noted that both this enclave and the host gneiss have anomalously high 87Sr/86Sr compared with the majority of the Adie Inlet gneisses. This led Pankhurst (1983) to speculate that the protolith at this locality was at least partly sedimentary, with an ancient provenance. Sm–Nd analyses of this and other similar granitoid gneisses from Adie Inlet broadly support this interpretation and give depleted mantle Nd model ages of ca. 1,550 Ma with ɛNd of −7 at ca. 258 Ma (Millar et al. 2001; Hole 1986). Hole (1986) concluded, on the basis of the Sr and Nd data, combined with major and trace element geochemistry, that the gneisses represent partial melts from a garnet-rich intermediate metamorphic rock at depth.
Joerg Peninsula gneiss, R.2602.1
Gneisses from the Joerg Peninsula (Fig. 1) are divided into three lithological types: biotite gneiss, granodioritic gneiss and granite gneiss (Hole et al. 1991). The selected sample of granite gneiss is foliated and contains small porphyroblasts of K-feldspar in a leucocratic matrix comprising plagioclase, muscovite, biotite and quartz (Hole 1986). The gneisses are cut by the relatively undeformed Late Triassic 206 ± 6 Ma (Rb–Sr whole rock isochron: Hole et al. 1991) Pylon Point granite, which yields a U–Pb zircon age indistinguishable from the Rb–Sr age (BAS unpublished data).
Zircons are prismatic, euhedral and have high aspect ratios of up to 5:1. Under CL, the zircons exhibit complicated core and rim structures (Fig. 3b). Rounded cores are only rarely present (e.g. grains 3 and 5, Fig. 3b). More common are angular cores with fine-scale, strongly luminescent growth zoning (e.g. grains 8 and 9, Fig. 3b). The contacts between these luminescent cores and the ubiquitous relatively non-luminescent rims are angular, sharp, and cut across the zonation patterns in the cores. Grains 3 and 5 (Fig. 2b) both have rounded cores that are surrounded by a bright, zoned “outer” core and have an angular contact with the dark rim. Rims, although dark, exhibit faint fine-scale growth zoning, and often comprise the majority of the zircon grain. In addition, the sample contains euhedral, prismatic grains up to 200 μm-in length, which have no cores and have similar characteristics to the dark rims (Fig. 3b). Similar grains make up around 15–20% of the total zircon population, suggesting that nucleation of new zircon occurred at the same time that the CL-dark zircon rims grew.
Prior to this study, the best estimate of the age of the Joerg Peninsula gneiss was 236 ± 7 Ma (mid-Triassic; Rb–Sr whole-rock isochron: Hole et al. 1991). Our new SHRIMP analyses from rims do not yield a concordia age due to some common Pb in the analyses. However, a weighted mean of the 206Pb/238U ages yields a Mid-Triassic age of 237 ± 2 Ma (Fig. 5a). Five cores yield 206Pb/238U ages of 497 ± 12 Ma, 568 ± 36 Ma, 605 ± 14 Ma, 1037 ± 22 Ma and a 207Pb/206Pb age of 1,687 ± 14 Ma (Table 1).
Mount Eissenger leucosome, R.5257.1
Layered, polyphase folded gneisses crop out at the eastern end of Mount Eissenger (Fig. 1) and on the southeast flank of Mount Allan, and are separated from Cretaceous gabbro by a high-strain zone (Vaughan and Millar 1996). The gneisses have a banded appearance with centimeter-scale compositional layering, and locally contain angular mafic fragments as well as more rounded inclusions of rhyolitic and pelitic material. These inclusions probably represent xenoliths of wall rock incorporated in individual magmatic sheets before they recrystallized to gneiss (APM Vaughan unpublished data). In other areas, field relations suggest that the leucocratic bands within the gneiss are leucosomes that possibly represent in situ melting of an orthogneiss protolith (APM Vaughan unpublished data). Zircons were separated from one such leucocratic band, which is granitic in composition, medium-grained, and has undergone pervasive post-crystallization ductile deformation.
The zircons are large (commonly > 300 μm in length), euhedral, stubby to prismatic, and show complicated internal structures under CL (Fig. 3c). The centers of grains contain moderately bright cores with fine-scale growth zonation overgrown by relatively non-luminescent zircon with diffuse growth zonation. The contact between the core and the surrounding zircon is convoluted and highly lobate (e.g. grain 13, Fig. 3c). Non-luminescent zircon also forms acicular grains without any inherited core. The non-luminescent overgrowths are in turn ubiquitously overgrown by thin, < 10 μm rims with moderate luminescence and growth zoning (e.g. grain 1, Fig. 3c). These outer rims form the well-developed crystal facets. The contacts of these rims cut across growth zones within the inner rims, suggesting that the latter were partially dissolved and resorbed before the outer rims grew.
SHRIMP analyses documented in Millar et al. (2002) show that the inherited cores have a simple age distribution, confirming that the gneiss has an igneous protolith with an age of 422 ± 18 Ma (Late Silurian). Formation of the non-luminescent overgrowths occurred at 228 ± 3 Ma (mid–Late Triassic) and was followed by a final stage of zircon growth accompanying metamorphism in Late Triassic–Early Jurassic times at ca. 202 Ma (Millar et al. 2002). Sm–Nd analysis of this rock yields a depleted mantle Nd model age of ca. 1,030 Ma with ɛNd of −0.1 at the time of migmatization, ca. 228 Ma (Millar et al. 2001).
Mount Nordhill, leucocratic gneiss, R.4552.9
A complex of paragneiss disrupted by gneissic leucogranite sheets, gneissic K-feldspar megacrystic granites and homogeneous biotite-orthogneisses, is exposed at Mount Nordhill (Fig. 1; Wever et al. 1995). The selected sample is from a gneissic leucocratic sheet containing the assemblage K-feldspar, quartz, plagioclase and biotite (Wever et al. 1994). Zircons from are subhedral and range in shape from stubby to prismatic, and in size from ca. 50 μm to > 300 μm. Under CL, all grains exhibit cores and rims; for approximately 70% of the grains, the cores make up a large proportion of the grain and subsequently control its size and shape (Fig. 3d). In most grains the luminescent cores exhibit a growth-zoning pattern and their contacts with the generally featureless non-luminescent rims is highly irregular (e.g. grain 24, Fig. 3d). This texture strongly resembles that of the Mount Eissenger sample (above). New SHRIMP U–Pb analyses of zircon rims yielded a mid-Jurassic concordia age of 166 ± 3 Ma (Fig. 5b). These are interpreted to have grown from a melt. The highly resorbed cores include an inherited component that is dominated by latest Early Jurassic ages, and yield a concordia age of 178 ± 3 Ma. Other ages for the inherited cores range from ca. 215 Ma up to ca. 1,500 Ma (Fig. 4b; Table 1). Depleted mantle Nd model ages of ca. 1,605 Ma and ɛNd values of −8.4 at the age of emplacement at ca. 166 Ma, together with the peraluminous chemistry for the rock, suggest that the melt may be derived through crustal anatexis of the paragneisses that they cut, or similar rock nearby (e.g. sample R.4293.1 detailed below: Wever et al. 1994; Millar et al. 2001).
Welch Mountains paragneiss, R.4293.1
Quartzitic paragneiss forming part of a sequence of quartz-rich to semi-pelitic migmatitic paragneiss, crops out at Solem Ridge near Mount Jackson in the Welch Mountains (Fig. 1; Singleton 1980). A sheeted complex of gneissic leucogranitic, biotite orthogneiss and granite pegmatite intrudes the paragneisses. These paragneisses and similar rocks in the vicinity are thought to be the source for the gneissic leucogranite sheets exposed at Mount Jackson and Mount Nordhill (R.4552.9 above). The paragneiss (R.4293.1) yields a 1,707 Ma depleted mantle model age and ɛNd of −9.6 at 166 Ma (Millar et al. 2001). Analyses of paragneiss throughout the Mount Nordhill and Mount Jackson area all have a similar isotopic character (Millar et al. 2001).
Zircons from the paragneiss are rounded and commonly have a pitted surface. Under CL the grains show a wide variety of brightness and zoning characteristics (Fig. 3e). The rounded nature of the grains, coupled with the dissimilar and varied CL zoning characteristics from grain to grain, suggest that these grains were worn and abraded during sediment transport and suggest a lithologically varied source for the sedimentary protolith. No new zircon grew during metamorphism, and zircon dissolution during metamorphism is thought unlikely as pitting of the zircon surface is thought to be a product of sedimentary abrasion. New SHRIMP U–Pb ages show a detrital zircon age distribution that is dominated by ca. 500 Ma to ca. 650 Ma zircons, but also has important contributions of zircons with age ranges between ca. 1,000–1,150 Ma and ca. 1,600–1,800 Ma (Fig. 4c).
Hf isotope data
Adie Inlet gneiss
Circa 258 Ma rims from three separate zircon grains and two other zircon grains where the time-resolved portion of the analysis is interpreted to record ablation of the rim, yielded similar 176Hf/177Hf ratios (Table 2; Fig. 6a). Only one rim analysis (UNK.1) is out of analytical uncertainty from the other four analyses. The corresponding core analysis from this grain is highly evolved, and inadvertent mixtures between the core and rim during an unpredictable ablation could account for its slightly lower 176Hf/177Hf ratio of the rim compared with the other rim analyses. Excluding this analysis, the rims yield 176Hf/177Hf of 0.282480 ± 109 (2 SD, n = 4) which corresponds to ɛHf(258) of −5.0 ± 4.0 (Fig. 6a). Core analyses are variable both in age and 176Hf/177Hf (Table 2). Some cores have a 176Hf/177Hf value that is indistinguishable from that of the average 176Hf/177Hf for the rims (e.g. grains 20 and UNK2; Table 2). Some grains, however, show significant differences between the core and corresponding rim (Fig. 6a). For grain UNK 1, the core gave 176Hf/177Hf value of 0.281619 ± 81 (2σ) whilst the rim gave 176Hf/177Hf of 0.282337 ± 71 (2σ). This corresponds to a difference of 25 epsilon units between the core and the rim analysis, when calculated at 258 Ma.
Joerg Peninsula gneiss
Eight of eleven rims have indistinguishable 176Hf/177Hf, within analytical uncertainty. The other three rims have higher 176Hf/177Hf (Table 2; Fig. 6b). The rims yield a 176Hf/177Hf average of 0.282478 ± 142 (2 SD, n = 11) and no distinction can be made between the 176Hf/177Hf of the luminescent inner and the non-luminescent outer rims. The 176Hf/177Hf variation of the rims equates to an ɛHf(238) range from −0.4 to −8.0; greater than would be expected through analytical uncertainty alone. The analyzed cores yield lower 176Hf/177Hf values than the majority of the zircon rims, the difference being greater than analytical uncertainty (Fig. 6b). For grain 3 the 176Hf/177Hf difference between core and rim corresponds to a shift of 11 ɛHf units at 238 Ma, the crystallization age of the zircon rim.
Mount Eissenger leucosome
The ca. 227 Ma-old, earliest Late Triassic, non-luminescent zircon that overgrows the partially resorbed cores yields an average 176Hf/177Hf value of 0.282589 ± 133 (2 SD, n = 13). Many of the rim analyses have 176Hf/177Hf values that differ from each other by more analytical uncertainty. Excluding one highly anomalous result (grain 1.1; Table 2) the average is 0.282589 ± 100 (2 SD, n = 12). The highly resorbed ca. 422 Ma Silurian cores yield more variable 176Hf/177Hf than the rims but the average 176Hf/177Hf value of 0.282654 ± 244 (2 SD, n = 10) is indistinguishable from that of the rims (Fig. 6c). Two of the ten grains where both core and rim were analyzed (grains 12 and Hf grain 2; Table 2) have 176Hf/177Hf values which differ by more than analytical uncertainty.
Mount Nordhill leucocratic gneiss and Welch Mountains paragneiss
The 176Hf/177Hf ratios for the ca. 166 Ma rims are somewhat variable from grain to grain, with some grains differing by more than analytical uncertainty, but yield an average value of 0.282447 ± 98 (2 SD, n = 6). Overall, the 176Hf/177Hf values for the cores are more variable than those of rims but on average, regardless of age, they are indistinguishable from those of the ca. 166 Ma rims (Fig. 6d), yielding values of 0.282460 ± 281 (2 SD, n = 10). Grains from the Welch Mountains sample yielded 176Hf/177Hf values that are generally lower than those of the Mount Nordhill rims (Fig. 6d).
Hf isotopes, anatexis and the source of crustal melts
At the site of crustal melting, hafnium within the melt is either derived from (a) dissolved zircon or, (b) the breakdown of less hafnium-rich minerals such as titanite, amphibole, pyroxene and other accessory minerals. This second source of hafnium is particularly important where the source rock is zircon poor. A significant factor that needs to be considered for non-zircon sources of hafnium is that they also contain higher concentrations of lutetium and so may have significantly higher 176Hf/177Hf than that derived from zircon in the same rock.
The range of hafnium values obtained from zircon that grew from a melt determine how isotopically homogenous it was. When these values are compared with those from the inherited component together with an assessment of zircon texture, an analysis of the anatectic processes at work can be made. For instance, if every zircon that grew from a particular melt had an identical Hf-isotope signature one could assume that the melt was isotopically homogenous. If this Hf-isotope signature is indistinguishable from the inherited component and there is abundant textural evidence for zircon dissolution, in situ melting and a closed system is indicated. Isotopic heterogeneity of zircons that grew from a particular melt would be indicated by significant variation in their Hf-isotope composition. In such instances, mixing from isotopically different sources and that each zircon is sampling small melt volumes could be implied.
Examining the textures and the range of 176Hf/177Hf in the zircons and any inherited component can therefore determine the degrees of melt homogeneity and the degree of mixing from isotopically different sources. In the sections below an attempt is made to assess the most likely sources and processes in operation during the generation of crustal melts in the Antarctic Peninsula.
Hf isotopes from samples with abundant inherited zircon and dissolution textures
Based on the study of Williams (2001), the zircon core–rim textures from both the Mount Eissenger leucosome and Mount Nordhill leucocratic gneiss samples demonstrate that the cores were partially dissolved in a melt before the growth of the rims. Without doubt, this texture indicates that Hf must have been liberated into the melt by zircon dissolution during migmatization. For these two samples, irrespective of age, the core and rim ɛHf and 176Hf/177Hf are, on average, indistinguishable. This observation is consistent with the Hf budget of the melt being controlled by zircon dissolution and that the proportion of Hf released from the zircon was large enough to swamp that derived from other sources.
Although the averages are identical, there is significant scatter in core and rim values suggesting relict isotopic heterogeneity is preserved from the inherited source(s) and in the melt. Generally, the spread in 176Hf/177Hf is less for the rims than the cores (Fig. 7a, b) but the rims exhibit a larger range of 176Hf/177Hf than one might expect from closed system melting and homogenization. However, excluding single outlying results from both the Mount Eissenger leucosome and Mount Nordhill leucocratic gneiss samples, the rims have 176Hf/177Hf compositions that are, within a range of 5 epsilon units, consistent from grain to grain (Fig. 7a, b). This suggests some isotopic homogenization occurred within the melt. For example, consider individual zircon grains from the Mount Eissenger leucosome sample that yield core and the rim analyses which differ by more than analytical uncertainty. Core analyses that yield extreme ɛHf values, at either end of the range measured for all the inherited grains, have corresponding rim analyses that sit within the main cluster of analyses (grains 12 and Hf grain 2; Table 2). Assuming the Hf budget is largely controlled by the dissolved zircon, had mixing and homogenization not occurred, then the rim analyses should also have yielded extreme ɛHf values, at either end of the range. Therefore a degree of Hf isotope homogenization was achieved in the melt.
The following hypothesis is proposed for the Mount Eissenger and Mount Nordhill samples: zircons that crystallized from the melt scavenged their elemental Hf and Hf isotope signatures primarily from zircon dissolved during anatexis. Some of this zircon survived as a partially dissolved inherited component in the melt. The rims are likely to record the 176Hf/177Hf of the melt; if Hf-rich minerals other than zircon contributed to the Hf budget of the melt, they had 176Hf/177Hf indistinguishable from the range of 176Hf/177Hf values measured in the inherited zircon, and thus the two possible sources cannot be distinguished. During anatexis, some degree of Hf isotope homogeneity was most likely achieved through small-scale melt migration. Complete Hf isotope homogeneity was not achieved and some zircon possibly grew from small melt volumes that either preserved isotope heterogeneity from a single protolith or, more likely, melt sourced from different protoliths each with a different isotope character.
More specifically, the Mount Eissenger leucosome has a simple zircon inheritance, either from a single ca. 422 Ma protolith with a large Hf-isotope variation, or several ca. 422 Ma protoliths with different Hf isotope compositions. Magmatic zircons that crystallized in the leucosome have, on average, ɛHf(227) of −1.8, corresponding to a t DM model age of 970 Ma, which is indistinguishable from the average t DM Hf model age of the inherited zircon component and broadly equates to the t DM Nd model age of ∼ 1,030 Ma. Therefore Hf isotopes of the inherited and magmatic zircon components indicate in situ melting.
The ages and age distribution patterns of the inherited zircon from the Welch Mountains paragneiss are not consistent with it being a source for the Mount Nordhill gneissic leucocratic sheet (Wever et al. 1994; Fig. 4); inherited zircon in the Mount Nordhill gneissic leucogranite is dominated by ca. 180 Ma zircons, whereas the Welch Mountains paragneiss is dominated by 500–600 Ma and older zircons. Although less conclusive than the U–Pb data, the small difference in the t DM Nd model ages for the Welch Mountains paragneiss and the Mount Nordhill Leucocratic gneiss is consistent with this interpretation. Like the Nd data, the Hf isotope composition of the Welch Mountains paragneiss detrital zircon grains are, on average, more evolved than both the inherited and magmatic zircon from the leucocratic sheet. However, the Hf isotope data do not rule-out the Welch Mountains paragneiss as a contributing source. For the Hf primarily derived from minerals other than zircon, evolution of the whole rock (an approximation of the Hf isotope composition from such minerals) prior to metamorphism could account for the resultant, more juvenile, Hf isotope composition of the zircon rims from the Mount Nordhill leucocratic gneiss. However, textural evidence, as argued above, suggests this was not the case and that the dissolved zircon controlled the Hf budget of the melt. Altogether, the geochronological and isotope data reveal that melting was of a sedimentary source(s) and that melt transport has emplaced the sheet into the Welch Mountains paragneiss. The source is either not exposed or has not been recognized.
Hf isotopes from samples with abundant inherited zircon but limited dissolution
On textural grounds, it is clear that the dissolution of inherited zircon during anatexis is less pronounced for the Adie Inlet gneiss sample. Commonly, new zircon overgrew rounded and elongate inherited grains and only rarely are there examples of irregular interfaces between core and rim that are indicative of zircon dissolution, suggesting that that rims may have overgrown originally detrital grains contained within the gneiss. Like the Mount Eissenger and Mount Nordhill samples, the rims have a degree of variation in their 176Hf/177Hf compositions from grain to grain. This variation is less than that recorded from the inherited component (Fig. 7c), indicating that the Hf isotopes within the melt were also partially homogenized.
Inspection of the average 176Hf/177Hf values of the cores and rims, suggest that the zircon rims require a less-evolved component than can be obtained from the inherited cores (Fig. 6a). This could suggest an open system and mixing of melt derived from the isotopically distinct domains within the Adie Inlet gneisses, as indicated by Sr and Nd whole rock geochemistry, with that derived from the inherited zircon component. Given that less zircon dissolution occurred during anatexis, derivation of some Hf from minerals other than zircon would be more likely to influence the Hf budget of the melt and may also account for the apparently more juvenile rims. We suspect that the Adie Inlet gneiss formed at least in part by in situ melting of its protolith(s), and that the inherited zircons contributed some of the Hf to the melt, as is indicated from rare dissolution textures seen in the CL images, but until further work is carried out, the evolution of the Adie Inlet gneiss remains unclear.
Hf isotopes from samples with rare inherited zircon
The low abundance of inherited zircon within the Joerg Peninsula gneiss sample suggests that it represents a discrete granitoid intrusion rather than the product of localized anatexis and migmatite formation. Intrusion was likely to be complex given the generation of distinct early luminescent inner and later non-luminescent rims. This zircon texture could indicate multiple phases of intrusion in the mid-Triassic, at 238 ± 5 Ma. The Hf isotope compositions for luminescent and non-luminescent Triassic growth phases are, on average, indistinguishable, suggesting a common source. However, both types of zircon exhibit a range of 176Hf/177Hf that equates to 8 epsilon units (Fig. 7c). Such variation supports the possibility of partially mixing of magma batches, each with a distinct Hf isotope composition. The inherited zircons have much lower 176Hf/177Hf (Fig. 6b), and due to their low abundance, could have been picked up from wall rock during ascent and emplacement of the granite magma. Like the Adie inlet sample, a contribution from minerals other than zircon could account for the juvenile character of the Triassic zircon. However, the lack of zircon inheritance does not permit further exploration.
New U–Pb zircon geochronology and Hf isotopes analyses of zircon in the context of the evolution of the Antarctic Peninsula
The detrital zircon age patterns and Hf isotope signatures from the Welch Mountains paragneiss shows that the detrital zircons with an age of ca. 1,200 Ma and younger were originally formed from material with an average mantle separation age of approximately 1,300 Ma (Fig. 7a). Crust of this age, with ɛHf of ca. +10 at 1,200 Ma (BAS unpublished data), is exposed at Haag Nunataks, situated approximately 750 km southwest from the Welch Mountains in Eastern Ellsworth Land. Based on Nd and Sr isotope ratios it has long been proposed that crust with a similar isotope signature was involved in the petrogenesis of Antarctic Peninsula granitoids (e.g., Millar et al. 2001). Should these zircons be derived from basement to the Antarctic Peninsula, then our Hf isotope data support the conclusions reached from the Nd and Sr data. Importantly, some of the zircon populations can be further subdivided based on their Hf isotope signature. For instance, the ca. 662 Ma population (zircons with 206Pb/238U ages within error of 662 Ma) has zircons with ɛHf values of approximately 2.5 and could have formed by the reworking crust like that at Haag Nunataks. The population also contains several zircon grains that are less-evolved and require a source that is either a mixture of that derived from crust like that at Haag Nunataks and a less-evolved, possibly mantle-derived source, or a different, more juvenile source than that at Haag Nunataks. One zircon grain yields a much more negative ɛHf value of −10.8 (Fig. 7b). Although this zircon crystallized at ca. 662 Ma, the negative ɛHf value suggests that the melt was predominantly sourced from Palaeoproterozoic material and therefore probably originated from crust outside of the Antarctic Peninsula. As a note of caution, the other detrital grains could also be recycled in the sedimentary system and have also originated from outside of the Antarctic Peninsula.
For the Adie Inlet gneiss, one 1,868 Ma grain with ɛHf of −11 requires an Archaean crustal source (Table 2). In a reconstruction of Gondwana, the closest potential source for zircons of this age would be in the Kaapvaal craton in Southern Africa (Poujol et al. 2003). Whether the zircons were recycled several times before being entrained in the Adie Inlet gneiss or originate from first cycle sedimentation cannot be resolved.
Although the cores of Mount Eissenger zircons are similar in age, they display a wide variation in ɛHf ratio (Fig. 7b). Such variation is statistically significant. An alternative to the possibility that the inherited grains represent zircon grains derived from different sources with distinct Hf isotope compositions, is that the variation represents temporal changes in 176Hf/177Hf in the magma chamber of the original igneous protolith during zircon crystallization. Such isotope variation probably reflects entrainment of different batches of magma with differing sources and Hf isotope ratios into the chamber. A similar variation in 176Hf/177Hf for zircon described by Griffin et al. (2002) is also attributed to magma mixing.
The new U–Pb age of 238 ± 5 Ma for the Joerg Peninsula orthogneiss is in agreement with the previously determined whole rock Rb–Sr isochron of 236 ± 7 Ma (Hole et al. 1991). The 166 ± 3 Ma for the age of the Mount Nordhill leucocratic dyke is unexpected, as the age of migmatization was expected to be comparable to the Triassic ca. 230 Ma or earliest Jurassic ca. 205 Ma events that are recorded in northeast Palmer Land (Millar et al. 2002). How widespread the c. 166 Ma metamorphism is, is at present, unclear. However, given the large quantity of ca. 180 Ma inherited zircon, the event post-dated initial magmatism related to the breakup of Gondwana, although overlapped with later silicic volcanism associated with the breakup (Silicic phase V2 of Pankhurst et al. 2000). Therefore, this event may represent decompression melting during uplift, facilitated by crustal extension and high heat flow that followed separation of the eastern Antarctic Peninsula from Gondwana.
Conclusions
We have measured the Hf isotope ratios of zircon by LA–MC–ICP–MS from four different samples of migmatite and granite gneiss and one possible migmatite-source rock from the Antarctic Peninsula. We have also presented SHRIMP U–Pb zircon geochronology for the samples where age information for the analyzed rocks is not already available. Our results show that Hf isotope studies offer potential for future investigation into the sources of crustal melts. For these samples studied from the Antarctic Peninsula:
-
1.
Zircon from migmatite and granite gneiss samples are complex and display core and rim structures under CL. The cores are older inherited zircon components that have suffered variable amounts of dissolution during anatexis. The rims are the same age and are interpreted to have grown from the melt generated during metamorphism.
-
2.
Zircon rims have 176Hf/177Hf that are similar from grain to grain in each sample. Significant isotopic variation is present but variation is less pronounced in the newly grown zircon than the inherited zircon and suggests Hf-isotope homogenization, possibly caused by melt migration. The variation preserved in the zircon rims may represent partial mixing of Hf derived from separate, isotopically distinct sources, or preserve original source heterogeneity.
-
3.
Where textural evidence suggests large degrees of dissolution of the inherited zircon component (Mount Eissenger leucosome and Mount Nordhill leucocratic gneiss samples), the 176Hf/177Hf of the inherited and newly grown zircon from the melt are, on average, indistinguishable. We suggest that the Hf budget was controlled by the dissolved zircon component and similar zircon at the source, and that the system was largely closed. The Mount Eissenger sample therefore probably records in situ migmatization at ca. 227 Ma of a ca. 422 Ma protolith. The Mount Nordhill sample does not have a Welch Mountains paragneiss source, as the paragneiss does not contain zircon signatures compatible with the inherited zircon age pattern. Melt migration allowed intrusion into the Welch Mountains paragneiss at 166 ± 3 Ma. Metamorphism and melt generation at ca. 166 Ma might reflect either high heat flow related to the generation of large volumes of plume-related silicic volcanism at this time or decompression melting following the break away of the eastern Antarctic Peninsula from Gondwana.
-
4.
Where textural evidence suggests that the inherited zircon has undergone smaller degrees of dissolution during anatexis (Adie Inlet gneiss and Joerg Peninsula gneiss samples), the 176Hf/177Hf values of the inherited and newly grown zircon are different. In both cases the melt apparently requires an additional, less evolved, source but can also be accounted for by Hf derived from minerals other than zircon, which because of their lutetium content may have evolved a higher 176Hf/177Hf than that of the average inherited zircon component. The evolution of these samples remains uncertain but the Adie Inlet gneiss may represent invasion of a melt derived from adjacent protoliths that are less evolved than the gneiss itself. The Joerg Peninsula gneiss probably reflects multiple intrusions of melt from a source with a somewhat variable Hf isotope composition, at 238 ± 5 Ma. Inherited zircon within the Joerg Peninsula gneiss may have resulted from wall-rock contamination during ascent and emplacement of the magma.
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5.
Hf isotopes of inherited zircons from all rocks, irrespective of age, were predominantly formed from melt derived from sources with late Mesoproterozoic mantle extraction ages.
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Acknowledgements
MJF acknowledges support from the Antarctic Funding Initiative (grant AFI 3/13 awarded to ILM and APMV) and skilled laboratory assistance by Vanessa Pashley at NIGL. ILM and APMV are indebted to the tireless assistance of the BAS operations group and field assistants that make fieldwork and sample collection in Antarctica possible. This work is a contribution to the BAS core programme Antarctica in the Dynamic Global Plate System, in particular the project Superterranes in the Pacific-margin arc (SPARC). Thorough and instructive reviews by Nigel Kelly and Tony Kemp and patient editing by Ian Parsons are greatly appreciated and have improved an earlier version of this manuscript.
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Flowerdew, M.J., Millar, I.L., Vaughan, A.P.M. et al. The source of granitic gneisses and migmatites in the Antarctic Peninsula: a combined U–Pb SHRIMP and laser ablation Hf isotope study of complex zircons. Contrib Mineral Petrol 151, 751–768 (2006). https://doi.org/10.1007/s00410-006-0091-6
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DOI: https://doi.org/10.1007/s00410-006-0091-6