Journal of Petrology Advance Access originally published online on December 1, 2007
Journal of Petrology 2008 49(1):79-105; doi:10.1093/petrology/egm071
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The Val Gabbro Plutonic Suite: A Sub-volcanic Intrusion Emplaced at the End of Flood Basalt Volcanism on the Kerguelen Archipelago
1Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, British Columbia, V6T-1Z4, Canada
2Department of Earth and Environmental Sciences, Universite Libre De Bruxelles CP160/02, Avenue F. D. Roosevelt 50, B-1050, Brussels, Belgium
3Anglo American Exploration (Canada) Ltd., Suite 800–700 West Pender Street, Vancouver, British Columbia, V6C-1G8, Canada
4Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
5Department of Geology, Whitman College, Walla Walla, WA 99362, USA
6Laboratoire De Geologie–Petrologie, Universite Jean Monnet, CNRS-UMR 6524, Saint-Etienne, France
RECEIVED JUNE 20, 2006; ACCEPTED OCTOBER 15, 2007
| ABSTRACT |
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The age, petrology, major and trace element geochemistry, and Sr–Nd–Hf–Pb isotopic geochemistry of basic and felsic rocks from the Val gabbro plutonic suite on the Kerguelen Archipelago, Southern Indian Ocean, are used to constrain the temporal and compositional relationships between sub-volcanic intrusions and flood basalt volcanism during the formation of a major oceanic island. The 4 km2 Val gabbro plutonic suite was emplaced at 24·25 ± 0·15 Ma (U–Pb zircon) into 25 Ma volcanic rocks of the Southeast Province, locally producing a large zone of overlying basaltic breccia. Cumulate basic–ultrabasic rocks are the dominant lithology in the intrusion, with horizontally layered peridotites at the base of the exposed part of the intrusion, overlain by vertically layered, coarse-grained plagioclase-bearing peridotites, melagabbros and equigranular gabbros. The intrusion was formed by repeated injections of relatively crystal-rich and crystal-poor magmas into an open-system magma reservoir. Strong geochemical and isotopic similarities between the fine-grained marginal microgabbros and cross-cutting felsic rocks and the hosting mildly alkalic basalts and trachytes of the Southeast Province indicate that they were derived from similar alkalic basaltic parental magmas, which were dominated by the enriched component of the Kerguelen mantle plume source. At 25 Ma, the change from tholeiitic–transitional to mildly alkalic basalts marks the terminal stage of flood basalt volcanism on the Kerguelen Archipelago. This compositional change was associated with deeper melting within the Kerguelen plume source, lower extents of melting, a decrease in magma supply, and the emplacement of high-level intrusions such as the Val gabbro plutonic suite.
KEY WORDS: Kerguelen Archipelago; Val gabbro plutonic suite; oceanic island; gabbros; sub-volcanic intrusion; alkalinity; Sr–Nd–Hf–Pb isotopes
| INTRODUCTION |
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The Kerguelen Archipelago in the Southern Indian Ocean contains some of the most extensive exposures of plutonic intrusions on an oceanic island. The first complete geological map of the Kerguelen Archipelago (Nougier, 1970
5% of the exposures. Subsequent detailed mapping and petrological studies focused mainly on describing the internal structure and petrology of the intrusive bodies (e.g. Nougier & Lameyre, 1973| GEOLOGICAL SETTING OF THE KERGUELEN ARCHIPELAGO AND SOUTHEAST PROVINCE |
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The 6500 km2 Kerguelen Archipelago, the emergent part of the Northern Kerguelen Plateau, is mainly composed of sub-horizontal basaltic lava flows (
85% of the exposed area) with the remaining area represented by plutonic rocks, Quaternary deposits, and glacial ice caps (Fig. 1). Based on recent Ar–Ar dating of basaltic whole-rocks and plagioclase separates, the major volcanic activity that formed the flood basalts currently exposed on the archipelago began at
29 Ma and continued until 24–25 Ma (Nicolaysen et al., 2000
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Plutonic rocks are found throughout the archipelago (Fig. 1) and were the focus of much of the original work on the geology of the Kerguelen Archipelago, especially the 150 km2 Rallier-du-Baty alkaline ring complex (Lameyre et al., 1976
The Southeast Province consists of the Jeanne d'arc and Ronarc'h Peninsulas (Fig. 2a). Two distinct magmatic series occur within the Southeast Province (Leyrit, 1992
; Weis et al., 1993
; Frey et al., 2000
) (Fig. 2a): (1) 25 Ma mildly alkalic basalts to trachytes that form the majority of the Jeanne d'arc Peninsula and the lower elevations of the Ronarc'h Peninsula; these volcanic rocks were originally referred to as the Lower Miocene series, based on early K–Ar dates in the range 20–22 Ma (Nougier et al., 1984
), although more recent Ar–Ar dates of 25 Ma (Frey et al., 2000
) indicate that the Southeast Province volcanic rocks are Oligocene (the currently accepted age for the base of the Miocene is 23·03 Ma; Gradstein et al., 2004
); (2) 6–10 Ma silica-undersaturated rocks (basanites to phonolites) that occur predominantly as plugs, domes, needles and minor flows mostly on the Ronarc'h Peninsula, and are referred to as the Upper Miocene series. The Southeast Province volcanic rocks are intruded by several small gabbroic (Gaby Island, Vallée des Neiges and Val) and felsic—monzonitic to syenitic—(Mont Berlioz and Mont Rouge) plutonic suites (Leyrit, 1992
). Based on the observed slopes to the lava flows and the abundance of dikes, Leyrit (1992
) proposed the existence of at least two major eruptive centres, one just offshore from Gaby Island in the west and one offshore from the Val gabbro plutonic suite in the east (Fig. 2a). A +10 to +15 mgal Bouguer gravity anomaly extends across the southeastern part of the Jeanne d'arc Peninsula and may be due to dense intrusive rocks at shallow depths related to the Val gabbro plutonic suite (Recq & Charvis, 1986
).
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| GEOLOGY OF THE VAL GABBRO PLUTONIC SUITE |
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The 4 km2 Val gabbro plutonic suite is located in the southeastern part of the Jeanne d'arc Peninsula (Cap du Challenger) (Fig. 2). The outcrops are concentrated along steep slopes leading down to the ocean, an area that is extremely difficult to access, and are also found inland along a NW–SE-oriented valley (Fig. 2b). The principal rock type within the exposed part of the Val gabbro plutonic suite is gabbro, which overlies peridotite. Peridotite forms the lower units of the plutonic suite near sea level at the base of the cliff and is characterized by horizontal igneous layering (Giret, 1983
1 m thick) are observed in the cliff-face leading down to the ocean and appear to extend below sea level. Finally, the intrusive rocks of the Val gabbro plutonic suite are cut by numerous fine-grained basic dikes (Fig. 3a), which typically have a sub-vertical orientation. These dikes probably represent the feeder system for overlying lava flows that were erupted following emplacement of the intrusion.
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| PETROLOGY AND MINERAL CHEMISTRY OF THE VAL GABBRO PLUTONIC SUITE |
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The results of a petrological and geochemical study of 17 samples from the Val gabbro plutonic suite were reported by Giret (1983
Representative electron microprobe analyses of olivine and clinopyroxene from the earlier series of samples (AG77) have been reported by Giret (1983
); however, there were no analyses of these minerals for the coarse-grained peridotites and melagabbros as they were not sampled in the earlier study. In this study, electron microprobe analyses of olivine and clinopyroxene were acquired on a fully automated Cameca SX-50 microprobe at the University of British Columbia, operating in wavelength-dispersion mode, with the following operating conditions: excitation voltage 15 kV; beam current 20 nA; beam diameter 5 µm; peak count-time 20 s; background count-time 10 s. Data reduction was done with the PAP
(
Z) method (Pouchou & Pichoir, 1991
) using natural standards. Compositions were typically determined from three grains of each mineral per sample with three point analyses per grain (one analysis in the core of the crystal, one from the crystal rim, and one additional analysis at an intermediate distance between the core and rim). The complete mineral chemistry results (78 olivine and 89 clinopyroxene analyses) are available in an Electronic Appendix, which can be downloaded at http://www.petrology.oxfordjournals.org/. All analyses reported are consistent with mineral stoichiometry.
Basic to ultrabasic intrusive rocks
The coarse-grained intrusive rocks are plagioclase-bearing peridotites to olivine melagabbros, subsequently referred to as peridotites in this study for simplicity, and contain abundant euhedral olivine and clinopyroxene (60–90 vol. %) ranging in size from 1 mm to >1 cm (Fig. 4). The peridotites are subdivided into two main rock types: wehrlites and olivine clinopyroxenites. The interstices between the larger grains contain discrete anhedral plagioclase and/or pyroxene grains (>1 mm grain sizes) in the wehrlites (samples MPC99-32, 34, 38, 39), or a fine-grained gabbroic matrix (<0·1 mm grain sizes) in the olivine clinopyroxenites (samples MPC99-35, 36, 40, 41, 43). Olivine core compositions are in the range of Fo76–86 in the wehrlites and Fo68–84 in the olivine clinopyroxenites; many of the olivine clinopyroxenites contain olivine that is distinctly more Fe-rich than in the wehrlites (Fig. 5a). Normal zoning (
Focore–rim = 6–10 mol %) is characteristic of more than half of the analyzed grains, with the remaining grains showing only minor to no zonation. Nickel contents of olivine cores range from 0·31 wt % NiO at Fo84·3 in the wehrlites to 0·1 wt % NiO at Fo70·9 in the olivine clinopyroxenites. Oscillatory zonation is characteristic of clinopyroxene in all olivine clinopyroxenites and clinopyroxene-rich melagabbros. Clinopyroxene core compositions show a limited range of Fe/Mg and plot within the restricted field for clinopyroxene phenocrysts from mildly alkalic basalts from the Crozier section on the Courbet Peninsula (Damasceno et al., 2002
) and especially from the high-MgO basalts and picrites sampled as cobbles from glacial moraines on the archipelago (Doucet et al., 2005
) (Fig. 5b). Alumina contents in clinopyroxene range from 1·1 to 4·6 wt % Al2O3. Sample MPC99-43 is distinctive because of the relatively low abundance of mafic minerals (40 vol. %), which are predominantly large (up to 1 cm diameter) euhedral clinopyroxene crystals with strong, oscillatory zonation. Olivine and clinopyroxene are interpreted to be cumulus minerals in the peridotites based on their high modal abundances, euhedral grain shapes, and Mg-rich mineral compositions. There is little evidence for textural equilibrium (e.g. straight grain boundary contacts, 120° triple junctions) between olivine and clinopyroxene grains, suggesting that cooling rates were sufficiently high at the level of emplacement of the Val gabbro to prevent subsolidus re-equilibration.
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The equigranular gabbros (MPC99-30, 31, 44, 45, 46, 58, 59 and 60) are dominated by highly variable proportions of millimetre-sized subhedral plagioclase and euhedral to equigranular, zoned clinopyroxene crystals (Fig. 4). There is no preferred alignment to the orientation of the plagioclase laths (width/length
1/3). Samples MPC99-45 and 59 are distinctive from the other equigranular gabbros; sample MPC99-45 contains abundant plagioclase (83% CIPW normative content) and sample MPC99-59 contains abundant Fe–Ti oxides. Olivine is typically a minor phase, or absent, except in MPC99-46, where fresh and/or altered euhedral olivine grains occupy up to 20 vol. % of the sample. Interstitial biotite forms 5 and 15 vol. % of samples MPC99-45 and 46, respectively. Alteration is minor in most samples, except MPC99-30, which contains
10 vol. % chlorite.
The microgabbros (MPC99-23, 28, 51, 52 and 54) and the subophitic microgabbros (MPC99-24, 25 and 26) are the finest-grained basic rocks in the Val gabbro plutonic suite (Fig. 4). In the microgabbros, both plagioclase and clinopyroxene are present as uniformly fine-grained crystals (<1 mm). Sample MPC99-52 is distinctive in that it contains a fine-grained matrix with abundant (
15 vol. %) coarser-grained (up to 6 mm) clinopyroxene and olivine crystals (Fig. 4), which vary from euhedral to irregular and resorbed in shape and which resemble the mafic crystals in the peridotites and melagabbros. The subophitic microgabbros contain 60–80 vol. % plagioclase, typically elongate (width/length
1/10), millimetre-sized and zoned, and 15–30 vol. % clinopyroxene, which is pink in plane-polarized light (titanaugite), weakly zoned to unzoned, and poikilitic. Minor amounts (<5 vol. %) of interstitial quartz and calcite occur in each of the examined samples and both minerals contain abundant acicular apatite and locally euhedral zircon grains.
Felsic intrusive rocks
The felsic intrusive rocks, including samples MPC99-47, 48, 49, 50, 53A (53a/A, 53 b/A, 53c/A), 56 and 57, are monzonites to quartz monzonites with grain sizes <1 mm. Plagioclase is commonly strongly zoned with altered sodic rims. Euhedral to anhedral alkali feldspar crystals are locally microperthitic and variably altered to fine-grained sericite. Green to brown amphibole is present in most samples as well as small clots of titanomagnetite and clinopyroxene that are interpreted to represent amphibole breakdown products during late-stage oxidation, a feature typical of plutonic rocks on the Kerguelen Archipelago (Giret et al., 1980
). Minor clinopyroxene, fayalitic olivine, and quartz are also present. Fe–Ti oxides, predominantly ilmenite, occur in most samples. Euhedral zircon and needles of apatite are typically present as accessory minerals. Sample MPC99-47 is notably more feldspar-rich than the other samples and does not contain quartz, and the feldspar in sample MPC99-56 is more extensively altered compared with the other felsic rocks. Sample MPC99-56 also contains abundant 1–3 mm diameter rounded clots of finer-grained igneous inclusions that are significantly more oxide- and plagioclase-rich than the matrix of the sample.
Volcanic rocks
Five volcanic rocks (MPC99-42, 53a/B, 53c/B, 61 and 62) representative of the host rocks to the Val gabbro intrusive complex were also sampled to investigate possible thermal and/or alteration effects related to emplacement of the gabbroic rocks and to compare with volcanic rocks from elsewhere in the Southeast Province. Local hornfelsing (1 cm thickness) of the host basalt is observed only in sample MPC99-53, which contains plagioclase-phyric alkali basalt in contact with the plutonic rocks (i.e. the contact runs through the sample). Sample MPC99-42 is a weakly plagioclase-phyric alkali basalt (<5 vol. % phenocrysts). Samples MPC99-61 and 62, taken 3 km to the NE of the exposed plutonic rocks (Fig. 2b), are strongly plagioclase-phyric alkali basalts (
15 vol. % phenocrysts) with large tabular plagioclase phenocrysts up to 1 cm in length (Fig. 4), which is typical of flows observed throughout the Southeast Province (Weis et al., 1993
; Frey et al., 2000
).
| AGE OF THE VAL GABBRO PLUTONIC SUITE |
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The previously reported ages for the Val gabbro plutonic suite are 39 ± 3 Ma for a gabbroic rock (sample AG78-04) and 27·4 ± 0·8 Ma for a felsic dike (sample AG78-31) [K–Ar whole-rocks; J. M. Cantagrel, unpublished data, cited by Giret et al. (1981
). That this average age of
25 Ma is equally valid for other volcanic rocks from the Southeast Province is corroborated by the Rb–Sr isochron age of
25 Ma reported for alkali basalts and trachytes by Weis et al. (1993
In light of the structural evidence for an intrusive origin for the Val gabbro plutonic suite and the coherent age of
25 Ma for volcanic rocks of the Southeast Province, we have (1) re-examined the original gabbroic sample that was dated (AG78-04) to assess the possible role of alteration on K–Ar systematics, and (2) determined the U–Pb ages of separated zircon and baddeleyite fractions from a subophitic gabbro (MPC99-24) from the intrusion. Sample AG78-04 is highly altered with abundant secondary chlorite, sericite and zeolites; it also contains significantly less K2O (0·16 wt %; Giret, 1983
) than equivalent rocks (equigranular gabbros) analyzed in this study (average K2O is 0·85 wt %). This confirms that alteration has resulted in significant K loss and thus the previously reported K–Ar date for this sample should not be considered geologically meaningful. Sample MPC99-24, a subophitic microgabbro from this study, contains microscopically visible euhedral zircon within interstitial quartz–carbonate patches. Zircon and baddeleyite were separated from a 3 kg split of the original sample using conventional crushing, grinding, Wilfley table, heavy liquids and Frantz magnetic separator techniques. The separated zircon grains were small (most <100 µm) and showed a range of aspect ratios from stubby, nearly equant grains to slender, high-aspect ratio (5:1) grains. Nearly all of the zircon grains were characterized by the presence of fluid inclusions. The separated zircon was split into two fractions for dissolution and analysis. About 10 grains, mostly fragments, of very fine-grained baddeleyite (<10 µm) were also present and all of this was analyzed as a single fraction. U–Pb isotopic analyses were carried out at the Pacific Centre for Isotopic and Geochemical Research at the University of British Columbia. The method for zircon and baddeleyite grain selection, dissolution, geochemical preparation, and mass spectrometry has been described by Mortensen et al. (1995
). Procedural blanks for Pb and U were 2 and 1 pg, respectively. Table 1 contains all U–Pb results from this study and U–Pb data are plotted on a conventional U–Pb concordia plot in Fig. 6. Errors attached to single analyses were calculated using the numerical error propagation method of Roddick (1987
) and decay constants used are those recommended by Steiger & Jäger (1977
). Compositions for initial common Pb were taken from the model of Stacey & Kramer (1975
). The errors on the ages are given at the 2
level. U–Pb data from the two zircon fractions are concordant and yield a total range of 206Pb/238U ages of 24·25 ± 0·15 Ma, which is interpreted as the age of crystallization of the subophitic microgabbro and thus of the Val gabbro plutonic suite. The U–Pb data from the single baddeleyite fraction are also concordant and the 206Pb/238U age is 23·9 ± 0·2 Ma. The relatively high error in 207Pb/235U for the baddeleyite fraction is due to the very low Pb concentration (Table 1) such that the blank correction has an impact on the calculated age. The U–Pb baddeleyite age is interpreted as a minimum age of crystallization and may reflect minor post-crystallization Pb loss.
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| WHOLE-ROCK SAMPLE PREPARATION AND GEOCHEMICAL ANALYTICAL TECHNIQUES |
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A total of 36 samples (23 basic and ultrabasic rocks, eight felsic rocks and five volcanic rocks) were prepared for geochemical analyses (sample locations are given in the Appendix). All weathered surfaces were sawn off and all fresh surfaces were systematically ground with sandpaper to remove any metallic traces of the saw-blade. The rocks were then reduced to millimetre and smaller sized pieces in a tungsten carbide hydraulic crusher by the percussion method (no grinding) and further reduced to a powder suitable for acid digestion in clean agate jars within a planetary mill.
Concentrations of the major elements and Rb, Sr, Ba, V, Ni, Cr, Zn, Ga, Y, Zr and Nb were determined by X-ray fluorescence (XRF) at the University of Massachusetts following the method of Rhodes (1996
). All samples were analyzed in duplicate and the reported value is the average of the two analyses; estimates of the analytical precision and accuracy have been given by Rhodes (1996
) and Rhodes & Vollinger (2004
). All other trace elements were analyzed by inductively coupled plasma mass spectrometry (ICP-MS: HP 4500) at the University of Göteborg, Sweden. For each sample, approximately 12 mg of sample powder was dissolved in a solution of 1·8 ml of HF (40%) and 1·2 ml of HNO3 (69%) for 48 h in sealed Teflon beakers on a hot plate. After evaporation, 1 ml of HNO3 (69%) and 2 ml of H2O (mQ) were added and the beakers were placed for 30 min in an ultrasonic bath. The resulting solution was put in a tube and an aqueous solution of 44 ml with 12 ppm Re and In was added. Each element was measured three times during a 1·5 s uptake on the ICP-MS system. Internal standard corrections were made with In or Re. After determining the blank and drift corrections, the counts/concentrations calibration line was calculated from measured counts and known concentrations of standards (89-170, AGV, K1919, BHVO, BIR, DNC and W2) and was then used to calculate element concentrations in the samples. Duplicates were made for six samples (MPC99-25, 32, 38, 45, 52 and 60). The relative differences between the two different measured concentrations for all duplicates are smaller than 5%, except for Lu (maximum 11%) and for U (less than 6% for five samples, but up to 16% for MPC99-38, which is a coarse-grained melagabbro with the lowest U concentration—0·10 ppm—of all the duplicates).
The Pb, Sr, and Nd isotopic compositions for 13 samples were measured at the Université Libre de Bruxelles on a Micromass 54 thermo-ionization multicollector mass spectrometer. For each sample, about 350 mg of powder was leached seven times with 6N HCl. The basic rocks were digested on a hot plate in closed Teflon beakers: 48 h in a solution of 10·5 ml of 6N HF and 1·5 ml of HNO3, and an additional 24 h in 10 ml of 6N HCl. Digestion of the acidic rocks was carried out in Teflon bombs locked in metallic bombs and placed in an oven at 180°C: 96 h in HF–HNO3 and 24 h in HCl [see Weis et al. (2006
) for a detailed description of the procedure]. Separations of Pb, Sr and Nd were made successively on chromatographic columns (Dowex 1 x 8, Dowex W50 and HDEHP resins, respectively) following the method of Weis et al. (1987
). For the Pb isotopic compositions, about 45 ng of Pb was loaded onto a single Re filament using the H3PO4–silica gel technique; for Sr isotopic compositions, about 400 ng of Sr was loaded on a single Ta filament; and for the Nd isotopic analyses, about 150 ng of Nd was loaded on a triple filament (Re and Ta). Sr isotopic ratios were normalized to 88Sr/86Sr = 0·1194 and Nd isotopic ratios were normalized to 146Nd/144Nd = 0·7219. The average 87Sr/86Sr value of the NBS 987 Sr standard was 0·710274 ± 13 (2
m on 18 samples) and analyses of the Merck Nd standard yielded 143Nd/144Nd = 0·511958 ± 18 (2
m on five samples). All Pb isotopic ratios were corrected for mass fractionation on the basis of analyses of the NBS 981 Pb standard for a temperature range between 1050°C and 1100°C.
For the Hf isotopic analyses, 250–300 mg of whole-rock powder for each of the 13 samples was dissolved following the procedure described by Blichert-Toft et al. (1997
). The powders were dissolved using sub-boiled HF and HNO3 in Savillex Teflon vials. After drying down the dissolved sample, concentrated HF was added to precipitate rare earth element (REE) fluoride salts to separate the REE from the remaining sample. High field strength elements (HFSE) were then separated from the matrix by using an anion exchange column, and Hf and Zr were isolated from the HFSE concentrate using a cation exchange column. The Hf isotopic compositions were analyzed in the static mode on a Nu Plasma multiple collector ICP-MS system (Nu 015) in the wet plasma mode at the Université Libre de Bruxelles [see Weis et al. (2007
) for a detailed description of the procedure]. Both Lu and Yb were monitored during the course of analysis for interference corrections on mass 176; the 172Yb beam was negligible. The measured Hf isotopic ratios were corrected for isobaric interference with Lu at mass 176 by monitoring the isotope 175Lu; the 176Lu interference was subtracted using a value of 37·69969 for 176Lu/175Lu (Rosman & Taylor, 1998
). During the analyses, replicate measurements of the Hf JMC 475 in-house standard gave 0·282164 ± 15 (2
m on 13 measurements) and 0·282173 ± 13 (2
m on 13 measurements) for the two analytical sessions, which is within the range of previously published values for this standard (e.g. Blichert-Toft et al., 1997
; Chauvel & Blichert-Toft, 2001
; Goolaerts et al., 2004
). For consistency, all values were normalized to 176Hf/177Hf = 0·282160.
| GEOCHEMISTRY OF THE VAL GABBRO PLUTONIC SUITE |
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The major and trace element chemistry of whole-rock samples from the Val gabbro plutonic suite is reported in Table 2 and the isotopic chemistry is presented in Table 3 (Sr, Nd, Hf) and Table 4 (Pb).
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Major element variations
Intrusive rocks of the Val gabbro plutonic suite, including new analyses from this study and from the earlier study of Giret & Beaux (1984
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The compositions of the microgabbros and subophitic microgabbros overlap with those of the host mildly alkalic basalts and many of the basaltic lavas analyzed from the Southeast Province (Fig. 7) (Weis et al., 1993
Fo80–85. The clinopyroxene-rich rocks (olivine clinopyroxenites) plot systematically towards the field for the measured clinopyroxene compositions (Fig. 7: see Na2O + K2O and CaO vs SiO2). The major element compositions of the equigranular gabbros are variable (Fig. 7), reflecting the variable modal proportion of plagioclase to clinopyroxene (± olivine and Fe–Ti oxides) in these rocks: (1) clinopyroxene-rich samples (MPC99-30, 31, 44, 58) trend towards the field for clinopyroxene compositions defined by the peridotites; (2) plagioclase-rich rocks (e.g. MPC99-45) have higher alumina contents (up to 21·2 wt %) characteristic of intermediate to calcic plagioclase; (3) sample MPC99-46, which has abundant olivine, plots towards the field for the peridotites and has elevated MgO (13·1 wt %) relative to all other equigranular gabbros; (4) sample MPC99-59, which has abundant euhedral Fe–Ti oxides, has high TiO2 contents (5·1 wt %). The correlation between modal abundances and whole-rock geochemistry for the equigranular gabbros suggests that they represent cumulates of primarily plagioclase and clinopyroxene, with the notable exceptions of samples MPC99-46 and 59, which also contain cumulus olivine and Fe–Ti oxides, respectively.
Trace element variations
There is a strong positive correlation between Nb, which shows a large variation in the sample suite from 2 to 104 ppm and is relatively immobile during low-temperature alteration, and incompatible elements that are sensitive to secondary alteration (e.g. K, Rb, and Ba) (Fig. 8). This demonstrates that most samples from the Val gabbro plutonic suite have remained closed since their time of crystallization without significant loss or gain of these mobile elements. All of the basic rocks and basalts from the Southeast Province are characterized by similar incompatible element ratios (e.g. K/Nb, Rb/Nb, Zr/Nb, Th/Nb), which is consistent with their formation from common parental magmas. When incompatible elements are compared, the peridotites and equigranular gabbros plot close to the origin of the graphs, as a result of accumulation of olivine and clinopyroxene and the dilution effect on incompatible elements (Fig. 8). The equigranular gabbros have slightly higher K (and Ba) concentrations for given Nb values than the peridotites and microgabbros (Fig. 8), which is probably due to accumulation of plagioclase in these rocks. Elevated Sr concentrations at low Nb contents for the majority of the equigranular gabbros, and especially the extremely high Sr concentration of sample MPC99-45 (915 ppm) (Fig. 8), are consistent with significant plagioclase accumulation. The effect of clinopyroxene accumulation in the peridotites and equigranular gabbros is demonstrated by their elevated Sc concentration, which is compatible in clinopyroxene, with decreasing Nb (Fig. 8) (note that samples with low Sc concentrations, <25 ppm, are relatively olivine-rich and clinopyroxene-poor). In contrast, the effect of clinopyroxene fractionation in the microgabbros and especially in basalts from the Southeast Province is shown by progressively decreasing Sc concentrations with increasing Nb.
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The felsic rocks have the highest incompatible element concentrations of the sample suite (e.g. up to 104 ppm Nb, 777 ppm Zr, and 18 ppm Th; Table 2). Incompatible element ratios in the felsic rocks vary considerably with respect to the other rock types of the Val gabbro plutonic suite. For example, Zr/Nb is similar, K/Nb and Rb/Nb higher, and La/Nb lower in the felsic rocks compared with the peridotites, gabbros and basalts (Fig. 8). These variations mostly reflect changes in the relative compatibility of some trace elements as a result of the crystallizing assemblage (plag ± ksp ± ilm ± amph ± fa ± cpx ± zirc ± apa), which is significantly different from that of the microgabbros and basalts (plag + cpx ± ol) discussed above. In particular, Nb is compatible in ilmenite in differentiated basaltic magmas (Jang & Naslund, 2003
Primitive mantle-normalized incompatible element patterns for all of the basic rocks in the Val gabbro plutonic suite and the host basalts are shown in Fig. 9. The cumulates have the lowest trace element abundances and flattest patterns, whereas the zircon-bearing subophitic microgabbros have the highest abundances and steepest patterns. Two plagioclase-bearing wehrlites (MPC99-34 and 38), two olivine clinopyroxenites (MPC99-40 and 41), and all of the equigranular gabbros have strong positive Sr anomalies (Fig. 9) and small positive Eu anomalies in chondrite-normalized plots (Eu/Eu* = 1·02 and 1·05 in the wehrlites, 1·14 and 1·15 in the olivine clinopyroxenites, and 1·07–1·15 in the equigranular gabbros; Table 2), which is consistent with the presence of cumulus plagioclase in these samples. The relatively small positive Eu anomalies compared with the Sr anomalies in these rocks suggest that the positive Eu anomaly provided by cumulus plagioclase is offset by the negative anomaly typically associated with cumulus clinopyroxene (e.g. McKay, 1989
). The small positive Ti anomaly in sample MPC99-59 correlates with the presence of accumulated Fe–Ti oxides (ilmenite). The microgabbros have primitive mantle-normalized patterns that are very similar to those of the mildly alkalic basalts from the Southeast Province (Weis et al., 1993
; Frey et al., 2000
) and the host basalts (Fig. 9), confirming that the microgabbros represent melt to near-melt compositions.
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Sr, Nd, Pb, and Hf isotopic compositions
Age-corrected isotopic ratios for acid-leached samples from the Val gabbro plutonic suite are plotted in Fig. 10 (age corrections are for in situ decay over 24 Myr, based on measured parent–daughter concentrations from non-leached powders reported in Table 2). Analyses of non-leached (NL) aliquots are reported for several samples in Table 3 (MPC99-34 and 53 a/A) and Table 4 (MPC99-34). The efficient removal of secondary alteration phases by leaching is demonstrated by the lower 87Sr/86Sr and higher 206Pb/204Pb and 208Pb/204Pb of the leached (measured) aliquots. Samples from the Val gabbro plutonic suite show a relatively restricted range of isotopic compositions, which suggests that all intrusive rocks are genetically related to parent magmas of broadly similar isotopic composition. Initial 87Sr/86Sr is negatively correlated with initial 143Nd/144Nd, and these ratios range from 0·70500 to 0·70535 and from 0·51254 to 0·51262, respectively. The initial
Nd and initial
Hf values are positively correlated, spanning a small range from –1·19 to +0·25 and –0·02 to 3·16, respectively. The Pb isotopic compositions are also positively correlated, with initial 206Pb/204Pb = 18·22–18·44, 207Pb/204Pb = 15·50–15·56, and 208Pb/204Pb = 38·76–39·08 (note the relatively large size of the 2
error in 207Pb/206Pb compared with the total range observed for the Val gabbro plutonic suite). Within the isotopic dataset, the peridotites show a small but systematic difference from the other samples (Fig. 10), with relatively low 87Sr/86Sr and high 143Nd/144Nd, 176Hf/177Hf and Pb isotopic ratios compared with the other rocks. In contrast, the equigranular gabbros are characterized by relatively high initial 87Sr/86Sr and low 143Nd/144Nd and 176Hf/177Hf (Fig. 10). The isotopic compositions of the microgabbros generally plot closer to the equigranular gabbros and those of the felsic rocks span the range from the peridotites to equigranular gabbros (Fig. 10). These small isotopic differences between the rock types in the Val gabbro plutonic suite are consistent with emplacement of distinct magma batches within an open-system sub-volcanic intrusion.
|
| DISCUSSION |
|---|
Prior to this study, it was considered that the Val gabbro plutonic suite formed from a tholeiitic parent magma on the Kerguelen Archipelago at 39 Ma (Giret & Lameyre, 1984
Layering and crystal contents of magmas related to the Val gabbro plutonic suite
The Val gabbro plutonic suite is probably a relatively small exposure of a much larger intrusion; however, it provides a window into high-level differentiation processes in a volcanic oceanic island. The peridotites at the base of the cliff-face leading into the ocean (Fig. 2b) contain prominent macroscopic horizontal igneous layering, which can be observed from the cliffs above. Thus the deeper, unexposed levels of the Val gabbro plutonic suite may consist of a layered ultramafic intrusion, consistent with the positive Bouguer gravity anomaly that increases in magnitude towards the location of the intrusion in the SE part of the Jeanne d'arc Peninsula (Recq & Charvis, 1986
). Vertically layered gabbros, including the fine- to medium-grained equigranular gabbros and the coarse-grained plagioclase-bearing peridotites and melagabbros in this study, are up to 100 m thick in the vicinity of Cap du Challenger and extend for
2000 m along the coastline to the NW (Fig. 2b). Vertical layering is not common in layered intrusions, but has been observed in bodies that represent solidified magma conduits (e.g. Falcon Lake intrusive complex, southeastern Manitoba, Canada; Mandziuk et al., 1989
). The presence in the Val gabbro plutonic suite of cumulate rocks with variable grain sizes, vertical modal layering, and prominent angular discontinuities suggests that they formed in response to repeated injections of magma with variable crystal contents along a fracture-controlled, sub-volcanic plumbing system during progressive dilation and contraction of the magma pathways (Giret & Beaux, 1984
). Centimetre-scale modal layering in the equigranular gabbros may be related to these repeated pressure fluctuations; minor shifts in phase boundaries as a result of pressure changes in a magmatic system can produce large variations in the modal abundances of precipitating crystals (e.g. Naslund & McBirney, 1996
).
The small grain size (millimetre-scale) of the layered equigranular gabbros is consistent with in situ formation of the cumulate rocks from injections of relatively crystal-poor to crystal-free magmas. In contrast, the large (>1 cm) olivine and clinopyroxene grains in the coarse-grained melagabbros to peridotites probably crystallized and grew at deeper levels below the current exposure of the intrusion. Based on olivine–melt equilibria (e.g. Roeder & Emslie, 1970
), the most Fo-rich olivines observed in the peridotites (Fo83–85; Fig. 5) indicate crystallization from magmas with
8–10 wt % MgO. These crystals were transported upwards when ascent rates were sufficiently high to overcome the negative buoyant force exerted by the dense, centimetre-sized olivine and clinopyroxene, akin to the well-documented positive correlation between eruption flux and olivine phenocryst size and abundance in Hawaiian basalts (e.g. Murata & Richter, 1966
). Few of the exposed volcanic rocks in the Southeast Province contain more than several modal per cent olivine and/or clinopyroxene phenocrysts (Weis et al., 1993
; Frey et al., 2000
) [notable exceptions are samples LVLK-70 and LVLK-88 of Weis et al. (1993
)]. This suggests that large olivine and clinopyroxene crystals, such as those observed in the Val peridotites, were mostly trapped within sub-volcanic and deeper magma chambers and that they were extruded with lavas only during periods of locally increased magma flux or supply. Rare high-MgO basalts and picrites (6–17 wt % MgO) containing abundant (5–20 vol. %) olivine and clinopyroxene phenocrysts were erupted on the Kerguelen Archipelago (Doucet et al., 2005
, 2006
); they have trace element and isotopic characteristics similar to those of the 24–25 Ma mildly alkalic basalts from the Southeast Province and Courbet Peninsula (Doucet et al., 2005
). Olivine core compositions in these high-MgO basalts and picrites (Fo74–87) overlap with those from the Val peridotites (Fo68–86) and their respective clinopyroxene compositions are strikingly similar (Fig. 5), indicating that there may be a petrogenetic link between these two sample suites.
Compositional gap in mildly alkalic silica-oversaturated volcanic and plutonic rocks on the Kerguelen Archipelago
There is a notable compositional gap in basic and felsic rocks from the Val gabbro plutonic suite (from 49 to 58 wt % SiO2) and a prominent, although smaller, compositional gap in volcanic rocks from the Southeast Province (from 52 to 56 wt % SiO2) (Fig. 7). The existence of a compositional gap between the basic and felsic rocks on the Kerguelen Archipelago has been known since the original geological studies on the archipelago (LaCroix, 1924
), mainly from the much younger Rallier-du-Baty ring complex on the southwestern part of the archipelago (Fig. 1), and was first referred to as a Daly gap by Watkins et al. (1974
). A Daly gap, or a bimodal distribution of basalt–rhyolite or alkali basalt–trachyte, occurs on many oceanic islands (e.g. Iceland, Ascension, Canary Islands) and a large number of proposals have been made to account for the missing intermediate members, including critical variations in physical properties such as viscosity and density (e.g. Schmincke, 1967
; Jones, 1979
; Geist et al., 1995
), large thermal and chemical changes produced by small changes in magma replenishment (e.g. Bonnefoi et al., 1995
), and remobilization of highly fractionated interstitial melt from the solidification front of crystallizing gabbros (solidification front instability) (Marsh, 1995
). More recently, Freundt-Malecha et al. (2001
) demonstrated that intermediate-composition plutonic fragments representing cumulate and melt compositions were erupted with composite rhyolitic–basaltic ignimbrites on Gran Canaria, a type locality for bimodal volcanism; thus it is clear that intermediate-composition magmas do form during fractional crystallization and are trapped in the conduit systems beneath some oceanic islands.
Are the felsic rocks in the Val gabbro plutonic suite related to the basic rocks by fractional crystallization? The Sr–Nd–Hf–Pb isotopic compositions of the analyzed felsic rocks (MPC99-47, 53a/A, 57) and microgabbro (MPC99-51) are similar (Fig. 10; Tables 3 and 4), which is permissive of such a relationship. Figure 7 shows fractional crystallization trends calculated with MELTS (Ghiorso & Sack, 1995
) for a starting composition equivalent to a microgabbro (MPC99-54) under the following conditions: fO2 = FMQ – 1 (where FMQ is the fayalite–magnetite–quartz buffer); starting water content is 0·75 wt % H2O; pressure is 1, 5, and 9 kbar. The choice of oxygen fugacity and water content is based on the experimental results of Scoates et al. (2006
) on the polybaric liquid-line-of-descent of mildly alkalic basalts on the Kerguelen Archipelago. The pressure range also corresponds to pressures used in the experiments of Scoates et al. (2006
), which were based on the phenocryst crystallization environments identified by clinopyroxene–melt thermobarometry on mildly alkalic basalts from the Crozier section on the Courbet Peninsula by Damasceno et al. (2002
). The MELTS trends for the three pressures in Fig. 7 terminate at 73–74% fractional crystallization and span the silica gap between the microgabbros and felsic rocks from the Val gabbro plutonic suite. The 1 kbar MELTS trend extends to higher SiO2 contents than the higher-pressure trends, but underestimates alkali and Al2O3 contents compared with the higher-pressures trends (Fig. 7). The 5 kbar MELTS fractional crystallization trend provides the best fit to the observed geochemistry from the Val gabbro plutonic suite, which is consistent with the conclusion of Scoates et al. (2006
) that high-pressure (>5 kbar) fractionation dominated by crystallization of high-Al clinopyroxene most closely reproduces the compositional variations of the 24–25 Ma mildly alkalic lavas on the Kerguelen Archipelago. The felsic rocks themselves are found as thin (<10 cm to 1 m), vertically oriented dikes that cut the basic rocks and overlying basaltic breccia (Fig. 2b). This suggests that they represent pathways for highly evolved melts, which is consistent with their formation by extensive fractionation deeper in the plumbing system below the exposed Val gabbro plutonic suite.
Where are the intermediate-composition lavas or plutonic rocks produced during fractional crystallization? Bimodal volcanism—trachytic flows and tuffs intercalated with trachybasalt—is preserved within the Ravin du Charbon and Jaune sections of the Jeanne d'arc Peninsula (Fig. 2b; see Frey et al., 2000
, fig. 2). Bimodal volcanism is also characteristic of the youngest volcanic activity (26 ka) on the archipelago within the northern ring complex of the large Rallier-du-Baty volcano-plutonic complex (Gagnevin et al., 2003
). In contrast, there is a nearly continuous compositional trend from trachybasalt to trachyandesite in the 24–25 Ma Crozier section (Damasceno et al., 2002
; Scoates et al., 2006
, fig. 4) and from basaltic trachyandesite to trachyte erupted from the <1 Ma Mont Ross stratovolcano (Weis et al., 1998
). The compositions of plutonic rocks from the Rallier-du-Baty northern ring complex also fill the gap between the bimodal alkali basalt–trachyte lavas (Gagnevin et al., 2003
). Thus, the geological evidence indicates that under the appropriate conditions alkalic silica-oversaturated magmatism may produce either bimodal products or a continuum of compositions. It is possible that the Daly gap documented in the Val gabbro plutonic suite may simply be a function of the relatively small area of intrusive rocks actually exposed; additional exposures could potentially yield evolved dikes with intermediate compositions. However, given that the gap mimics that also recorded by the Southeast Province lavas and the evidence for relatively high-pressure fractionation, the intermediate-composition magmas appear to have been trapped at depth during formation of volcanic rocks of the Southeast Province. Density–viscosity relations will have a major impact on the eruptibility of magmas (e.g. Marsh, 1981
; Geist et al., 1995
). Using the MELTS results discussed above, the density of the evolved melts decreases progressively with fractionation (e.g. from 2·68 to 2·47 g/cm3 at 5 kbar in the range of the observed silica gap from 49 to 58 wt % SiO2, a decrease of
8%; see inset in Fig. 11), which would favor buoyancy-driven flow. The viscosity of the evolved melts, however, increases substantially in the same interval, from 1·5 to 5·0 Pa s at 5 kbar (Fig. 11), thus helping to inhibit flow. Although other factors, such as magma crystallinity, will also play a role in restricting the upward flow of intermediate-composition magmas, the increased viscosity of evolved melts produced during fractionation at depth appears to be an important factor in the origin of a Daly gap in rocks from the Val gabbro plutonic suite. The fact that some intermediate-composition volcanic and plutonic rocks do occur elsewhere on the Kerguelen Archipelago indicates that other variables locally control eruptibility (e.g. vapor saturation).
|
Source of the parent magmas to the Val gabbro plutonic suite
The radiogenic isotopic compositions of samples from the Val gabbro plutonic suite are similar to those of the 24–25 Ma mildly alkalic basalts from the Kerguelen Archipelago (Fig. 12), including samples from the Southeast Province (Weis et al., 1993
|
Gabbroic sub-volcanic magma chambers at the end of flood basalt volcanism on the Kerguelen Archipelago
Recognition that the Val gabbro plutonic suite crystallized from mildly alkalic basaltic parental magmas and that the age of the intrusion is 24 Ma allows for a re-examination of the temporal relationship between volcanic and plutonic rocks on the Kerguelen Archipelago during flood basalt volcanism. Extensive glaciation and a regional southeasterly dip of the flood basalts of 2–5° exposes progressively older and deeper sections to the NW across the Kerguelen Archipelago for the 26–29 Ma tholeiitic–transitional basalts; this corresponds to a 5–6 km stratigraphic section through the upper part of the archipelago based on an average 3° dip. There are no known contemporaneous high-level gabbroic intrusions exposed within these older basaltic sections. In contrast, the 24–25 Ma mildly alkalic basalts that cover the eastern part of the Kerguelen Archipelago (maximum exposed thickness of
1000 m) are cut by a number of gabbroic intrusions that are interpreted to represent sub-volcanic intrusions to overlying (now-eroded) flows (e.g. Val and Gaby Island in the Southeast Province, and Montagnes Vertes on the Courbet Peninsula; Giret, 1983
The presence of sub-volcanic gabbroic intrusions also follows a distinct increase in the alkalinity of the erupted basalts (Fig. 13), which suggests a link with variations in melting history for basalts on the Kerguelen Archipelago. The first systematic appearance of alkalic basalts (alkalinity index >0) occurs within the upper 100 m of the Tourmente section (Frey et al., 2002
) (see location in Fig. 1). The Tourmente magmas segregated within the stability field of spinel peridotite, with the uppermost alkalic lavas representing lower degrees of melting and segregation at higher pressures than the transitional lavas in the lower part of the section (Frey et al., 2002
). The chemistry of the 25 Ma mildly alkalic lavas in the Southeast Province also indicates decreased extents of melting compared with the tholeiitic–transitional basalts on the archipelago, but also increased pressures of segregation within the garnet stability field (Frey et al., 2000
) and a significant role for fractionation of high-Al clinopyroxene at pressures corresponding to the crust–mantle transition zone beneath the archipelago (14–16 km) (Damasceno et al., 2002
; Scoates et al., 2006
). This change in basalt chemistry is primarily a function of thickening of the cooling lithosphere as the distance between the Northern Kerguelen Plateau and Southeast Indian Ridge increased during the period from
40 Ma to 25 Ma (i.e. from a ridge-centred setting to a distance of 400 km) (Frey et al., 2000
; Scoates et al., 2006
), which forced decompression melting within the Kerguelen mantle plume to progressively deeper levels. Following eruption of the exposed 24–25 Ma mildly alkalic basalts, sub-volcanic gabbroic intrusions such as the Val gabbro plutonic suite were emplaced, and signal the end of flood basalt magmatism on the Kerguelen Archipelago as volcanism related to the Kerguelen plume shifted location several hundred kilometres to the SE beneath the Central Kerguelen Plateau (Weis et al., 2002
).
|
| CONCLUSIONS |
|---|
This study of the Val gabbro plutonic suite in the Southeast Province of the Kerguelen Archipelago, a major oceanic island in the Southern Indian Ocean, provides constraints on the relationship between high-level sub-volcanic magma reservoirs and flood basalt volcanism. The intrusion consists principally of vertically layered mafic–ultramafic rocks that overlie horizontally layered peridotites with local fine-grained marginal gabbros and rare cross-cutting felsic dikes (monzonite to quartz monzonite). A precise U–Pb zircon age of 24·25 ± 0·15 Ma for a subophitic microgabbro is interpreted as the age of crystallization of the intrusion, which indicates that the Val gabbro plutonic suite is only slightly younger than the hosting 25 Ma mildly alkalic basalts of the Southeast Province. Strong major and trace element and Sr–Nd–Hf–Pb isotopic compositional similarities between the fine-grained marginal gabbros and cross-cutting felsic rocks with the Southeast Province volcanic rocks (basalts and trachytes) indicate that the parental magmas to the plutonic rocks belong to the mildly alkalic silica-oversaturated magma series on the archipelago. The petrological and geochemical variations of the vertically layered cumulate rocks (plagioclase-bearing peridotites–olivine melagabbros and equigranular gabbros) are consistent with those produced by injections of mildly alkalic basaltic magmas with variable crystallinity into a sub-volcanic magma plumbing system during repeated dilation and contraction of the magma pathways. Differentiated, sub-volcanic gabbroic intrusions such as the Val gabbro plutonic suite do not occur within the older 26–29 Ma transitional basalts on the Kerguelen Archipelago, but were emplaced only when volcanism on the archipelago changed to mildly alkalic compositions after 25 Ma. This increase in alkalinity is also associated with evidence for lower extents of melting, deeper melting, a change in source components towards a plume-dominated enriched composition, and the presence of discrete volcanic hiatuses within volcanic rocks of the Southeast Province. The emplacement and crystallization of the Val gabbro plutonic suite at 24 Ma signals the end of flood basalt volcanism on the Kerguelen Archipelago.
| SUPPLEMENTARY DATA |
|---|
Supplementary data for this paper are available at Journal of Petrology online.
| Appendix: Locations of Geochemical Samples from the Val Gabbro Plutonic Suite |
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Sample locations (latitudes and longitudes are given as decimal degrees) referenced from GoogleEarth, version 4.0.2093 (beta).
| ACKNOWLEDGEMENTS |
|---|
We are greatly indebted to the IFRTP (Institut Français pour la Recherche et la Technologie Polaire), now IPEV (Institut Polaire Français Paul Emile Victor), and the captains and crew of the Marion Dufresne II and the Curieuse for their critical support of fieldwork on the Kerguelen Archipelago. We are grateful to Gilbert Michon, W. Powell, and Jean-Yves Cottin for diligently undertaking the new sampling of the Val gabbro plutonic suite in February 1999 in an area where access is difficult. The microprobe analyses were carried out under the always capable supervision of Mati Raudsepp at the University of British Columbia. Many thanks go to Jim Mortensen and Rich Friedman at UBC for the careful U–Pb analyses of zircon and baddeleyite. The ICP-MS trace element analyses at the University of Göteborg, Sweden, would not have been possible without the guidance and patience of Bill Meurer. Edouard Foriers carried out the Hf isotope chemistry and Claude Maerschalk provided important assistance during all of the chemical preparation stages of samples for Sr–Nd–Hf–Pb isotopic work at the Université Libre de Bruxelles. Discussions with Mauro Lo Cascio concerning his experimental work on mildly alkalic basalts from the Kerguelen Archipelago were extremely useful. Reviews by Armin Freundt and an anonymous reviewer plus editorial comments by Colin Devey helped to improve the clarity of the final manuscript. This research was supported with funding to Scoates, Weis, and Mattielli from the Communauté Française of Belgium (Actions de Recherche Concertées ARC Convention 98/03-233), to Frey from US NSF Grant EAR9814313, and to Scoates and Weis by Canadian NSERC Discovery Grants.
*Corresponding author. Telephone: (604) 822-3667. Fax: (604) 822-6088. E-mail: jscoates{at}eos.ubc.ca
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), and volcanic rocks from the Kerguelen Archipelago (fields). The arrows point towards the composition of Southeast Indian Ridge (SEIR) MORB, which represents the depleted mantle reservoir. The isotopic composition of the 24–25 Ma Crozier basaltic section on the Kerguelen Archipelago, especially the radiogenic Pb isotopic composition, is considered to represent that of the enriched component of the Kerguelen mantle plume (Mattielli et al., 2002