Description: The eruption and storage temperatures of rhyolitic magmas are critical factors for understanding the mechanisms of their eruption and petrogenesis. Temperatures are particularly important when comparing the magmatic histories of hot-dry rhyolites from the Yellowstone-Snake River Plain (YSRP) and Iceland to cold-wet rhyolites such as the Bishop Tuff. Here we employ mineral pair oxygen isotope fractionations for estimating rhyolite temperatures independent of pressure and other compositional factors. We report high precision oxygen isotope analyses of quartz, pyroxene, magnetite, and zircon that we use to estimate crystallization and storage temperatures. Temperatures for YSRP and Icelandic rhyolites are highest for quartz-magnetite and quartz-clinopyroxene (~950 °C), with lower quartz-zircon (850 °C) temperatures that are similar to estimates of zircon saturation. The magnitude and pattern of these temperatures is consistent with crystallization from near-liquidus rhyolites. In contrast, oxygen isotope temperatures calculated for the Bishop and other "cold-wet" type tuffs define low ~760 °C temperatures for all three mineral pairs consistent with prolonged mineral residence at near-solidus conditions. Preservation of a down-temperature crystallization sequence of hot magnetite and clinopyroxene with colder zircon in hot-dry YSRP and Icelandic rhyolites suggest 〈1000 yr magma residence, where magnetite does not have sufficient time to diffusively equilibrate oxygen in a lower temperature melt. This is consistent with recently determined high precision U-Pb crystallization ages zircons from the same units indicating magma generation shortly before eruption.

Description: Finely acicular rutile intergrown with host quartz (rutilated quartz) is commonly found in hydrothermal veins, including the renown cleft mineral locations of the Swiss Alps. These Alpine cleft mineralizations reportedly formed between ~13.5 and 15.2 Ma (based on ages of rare hydrothermal monazite and titanite) at temperatures ( T ) of ~150–450 °C (based on fluid inclusions and bulk quartz-mineral oxygen isotope exchange equilibria), and pressures ( P ) of 0.5–2.5 kbar (estimated from a geothermal gradient of 30 °C/km). The potential of rutilated quartz as a thermochronometer, however, has not been harnessed previously. Here, we present the first results of age and T determinations for rutilated quartz from six locations in the Swiss Alps with vein country rocks that cover peak-metamorphic conditions between ~600 and 〈350 °C. Samples were cut and mounted in epoxy disks to expose rutile (~30 to 1400 μm in diameter) and its host quartz. Cathodoluminescence (CL) and backscattered electron (BSE) imaging of host quartz and rutile inclusions, respectively, shows internal zonations, which are nevertheless isotopically homogeneous. Newly developed secondary ionization mass spectrometry (SIMS) oxygen isotopic analysis protocols for rutile were combined with those established for trace elements (including Zr) and U-Pb ages in rutile, and Ti abundances in the host quartz. U-Pb rutile ages average 15.1 ± 1.7 Ma (2), in excellent agreement with previous accessory mineral geochronometers. Pressure-independent T estimates, calibrated for low-temperature conditions, from oxygen isotope fractionation between rutile and quartz in touching pairs are 310–576 °C. Individual rutile needles vary in Zr abundances beyond analytical uncertainties, but average Zr-in-rutile inversely correlates with oxygen isotopic fractionation between quartz and rutile. Linear regression of the data yields: \[ T(^\circ \hbox{ C })=\frac{26(\pm 9)}{0.07(\pm 0.01)-\hbox{ R\hspace{0.17em}ln\hspace{0.17em} }x}-273 \] with x = Zr ppm and R = 0.008314 (uncertainties scaled by the square root of the mean square of weighted deviates MSWD = 11; n = 9). This relationship supports previously recognized temperature-dependent Zr uptake in rutile, although widely used Zr-in-rutile thermometer calibrations based on high- T experiments are at variance with oxygen isotope exchange temperatures. By contrast, Ti-in-quartz lacks systematic relations with oxygen isotope temperatures. The discrepancy between low- T Ti-in-quartz thermometry on one side, and oxygen isotope and Zr-in-rutile thermometry on the other, suggests that Ti-in-quartz thermometry should be applied with caution for low- T (〈500 °C) rocks.