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Our ability to reconstruct the crystallization history of a given accessory mineral (i.e., geochronometers such as zircon, titanite, monazite, etc.)—and thus the geologic processes of its host—has increased severalfold over the past few decades; primarily through advances in precision, concurrent chemical analysis, throughput, and spatial resolution. In this contribution, we present a methodology that takes these advances a step further through the rapid characterization of a large number of accessory minerals at micron-scale resolution via laser-ablation inductively coupled plasma mass spectrometry. Our analytical setup employs an ultrafast washout laser (~1 ms; Element Scientific Laser) that can send individual, <5um ablation pulses to either one or both of two instruments: a Nu Plasma 3D mulitcollector ICP-MS and a Nu Vitesse time-of-flight ICP-MS. Because either ICP-MS can measure at the sub-ms timescale, every pulse can be analyzed at 100’s of Hz; 1D, 2D, or 3D analysis is possible, and data can be processed in a matter of minutes and hours, instead of days or weeks. We highlight the advantages of this methodology through examples of accessory phases in complex plutonic rocks and high-grade metamorphic terranes. 

In situ apatite U-Pb petrochronology and Sr-Nd isotope geochemistry requires well-characterized and matrix-matched references materials (RMs), yet only a few suitable apatite RMs are currently available. To ameliorate this issue, we determined the U-Pb, Sm-Nd, and Sr isotopic and elemental compositions of a suite of prospective apatite RMs using isotope dilution (ID) TIMS and laser ablation (LA) ICP-MS. The two RMs, from Morocco (MRC-1) and Brazil (BRZ-1), are cm-sized and available in significant quantities. The U-Pb ID-TIMS data yield an isochron age of 153.3 ± 0.2 Ma for MRC-1. This age is consistent with laser ablation split stream ICP-MS (LASS) analyses that produce an isochron age of 152.7 ± 0.6 Ma. The weighted mean of ID-TIMS analyses for 143Nd/144Nd analyses is 0.512677 ± 3, for 147Sm/144Nd is 0.10923 ± 9, and for 87Sr/86Sr is 0.707691 ± 2. The range and mean of TIMS Sm-Nd isotopic data are reproducible by LA-ICP-MS, but laser ablation Sr data are consistently offset towards more radiogenic values. For BRZ-1 apatite, ID-TIMS U-Pb analyses are dispersed, but a subset of the data yields a coherent age intercept of 2078 ± 13 Ma. The vast majority of LASS spot transects across the apatite produce an isochron that define a younger age of 2038 ± 14 Ma. We interpret this as incorporation of cryptic, younger altered domains within BRZ-1. Discordant U-Pb spot analyses are associated with chemically distinct cracks, likely a result of fluid infiltration. The weighted means of ID-TIMS analyses of BRZ-1 yield 143Nd/144Nd = 0.510989 ± 5, 147Sm/144Nd = 0.10152 ± 8, and 87Sr/86Sr = 0.709188 ± 3. The distribution of Nd isotopic compositions of this RM measured by LA-MC-ICP-MS analyses are comparable to TIMS analyses. By contrast, 87Sr/86Sr measurements by LA-ICP-MS are inaccurate and exhibit large uncertainties, but this RM can be useful for empirically correcting in situ 87Sr/86Sr measurements. The data indicate that MRC-1 apatite may serve well as a U-Pb, Sm-Nd, and Sr RM, whereas BRZ-1 apatite has the most potential as a Sm-Nd RM. These potential RMs provide new benchmarks for in situ apatite chemical analyses and inter-laboratory calibrations. 

Abstract This study addresses the question of how and where arc magmas obtain their chemical and isotopic characteristics. The Wooley Creek batholith and Slinkard pluton are a tilted, mid- to upper-crustal part of a vertically extensive, late-Jurassic, arc-related magmatic system in the Klamath Mountains, northern California. The main stage of the system is divided into an older lower zone (c. 159 Ma) emplaced as multiple sheet-like bodies, a younger upper zone (c. 158–156 Ma), which is gradationally zoned upward from mafic tonalite to granite, and a complex central zone, which represents the transition between the lower and upper zones. Xenoliths are common and locally abundant in the lower and central zones and preserve a ghost stratigraphy of the three host terranes. Bulk-rock Nd isotope data along with ages and Hf and oxygen isotope data on zircons were used to assess the location and timing of differentiation and assimilation. Xenoliths display a wide range of εNd (whole-rock) and εHf (zircon), ranges that correlate with rocks in the host terranes. Among individual pluton samples, zircon Hf and oxygen isotope data display ranges too large to represent uniform magma compositions, and very few data are consistent with uncontaminated mantle-derived magma. In addition, zoning of Zr and Hf in augite and hornblende indicates that zircon crystallized at temperatures near or below 800 °C; these temperatures are lower than emplacement temperatures. Therefore, the diversity of zircon isotope compositions reflects in situ crystallization from heterogeneous magmas. On the basis of these and published data, the system is interpreted to reflect initial MASH-zone differentiation, which resulted in elevated δ18O and lowered εHf in the magmas prior to zircon crystallization. Further differentiation, and particularly assimilation–fractional crystallization, occurred at the level of emplacement on a piecemeal (local) basis as individual magma batches interacted with partial melts from host-rock xenoliths. This piecemeal assimilation was accompanied by zircon crystallization, resulting in the heterogeneous isotopic signatures. Magmatism ended with late-stage emplacement of isotopically evolved granitic magmas (c. 156 Ma) whose compositions primarily reflect reworking of the deep-crustal MASH environment. 

Rhyolitic melt that fuels explosive eruptions often originates in the upper crust via extraction from crystal-rich sources, implying an evolutionary link between volcanism and residual plutonism. However, the time scales over which these systems evolve are mainly understood through erupted deposits, limiting confirmation of this connection. Exhumed plutons that preserve a record of high-silica melt segregation provide a critical subvolcanic perspective on rhyolite generation, permitting comparison between time scales of long-term assembly and transient melt extraction events. Here, U-Pb zircon petrochronology and 40 Ar/ 39 Ar thermochronology constrain silicic melt segregation and residual cumulate formation in a ~7 to 6 Ma, shallow (3 to 7 km depth) Andean pluton. Thermo-petrological simulations linked to a zircon saturation model map spatiotemporal melt flux distributions. Our findings suggest that ~50 km 3 of rhyolitic melt was extracted in ~130 ka, transient pluton assembly that indicates the thermal viability of advanced magma differentiation in the upper crust. 

Abstract Lavas erupted at hotspot volcanoes provide evidence of mantle heterogeneity. Samoan Island lavas with high⁸⁷Sr/⁸⁶Sr (>0.706) typify a mantle source incorporating ancient subducted sediments. To further characterize this source, we target a single high⁸⁷Sr/⁸⁶Sr lava from Savai’i Island, Samoa for detailed analyses of⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd isotopes and major and trace elements on individual magmatic clinopyroxenes. We show the clinopyroxenes exhibit a remarkable range of⁸⁷Sr/⁸⁶Sr—including the highest observed in an oceanic hotspot lava—encompassing ~30% of the oceanic mantle’s total variability. These new isotopic data, data from other Samoan lavas, and magma mixing calculations are consistent with clinopyroxene⁸⁷Sr/⁸⁶Sr variability resulting from magma mixing between a high silica, high⁸⁷Sr/⁸⁶Sr (up to 0.7316) magma, and a low silica, low⁸⁷Sr/⁸⁶Sr magma. Results provide insight into the composition of magmas derived from a sediment-infiltrated mantle source and document the fate of sediment recycled into Earth’s mantle.