Earthtime

Quantification of geological time represents one of the fundamental challenges for earth scientists as it permits the determination of rates of change, integration of disparate geological datasets and assessment of coincidence (or lack thereof) so often central to hypothesis testing. Knowing the age of certain rocks, be it a thick accumulation of volcanic lava or an extinction layer, allows us to say something about causality. The extinction of the dinosaurs at the end of the Cretaceous Period, ‘about’ 66 million years ago is the poster child for such cause-and-effect arguments. At ‘about’ the same time, a large asteroid struck what is now the Gulf of Mexico, however a series of voluminous volcanic eruptions in India are also ‘about’ the same age. Both are viable kill mechanisms, and both are closely correlated in time with the extinction, but knowing they are ‘about’ the same age is not good enough

High-precision geochronology confirms voluminous magmatism before, during, and after Earth's most severe extinction

The end-Permian mass extinction was the most severe in the Phanerozoic, extinguishing more than 90% of marine and 75% of terrestrial species in a maximum of 61 ± 48 ky. Because of broad temporal coincidence between the biotic crisis and one of the most voluminous continental volcanic eruptions since the origin of animals, the Siberian Traps large igneous province (LIP), a causal connection has long been suggested. Magmatism is hypothesized to have caused rapid injection of massive amounts of greenhouse gases into the atmosphere, driving climate change and subsequent destabilization of the biosphere. Establishing a causal connection between magmatism and mass extinction is critically dependent on accurately and precisely knowing the relative timing of the two events and the flux of magma. New U/Pb dates on Siberian Traps LIP lava flows, sills, and explosively erupted rocks indicate that (i) about two-thirds of the total lava/pyroclastic volume was erupted over ~300 ky, before and concurrent with the end-Permian mass extinction; (ii) eruption of the balance of lavas continued for at least 500 ky after extinction cessation; and (iii) massive emplacement of sills into the shallow crust began concomitant with the mass extinction and continued for at least 500 ky into the early Triassic. This age model is consistent with Siberian Traps LIP magmatism as a trigger for the end-Permian mass extinction and suggests a role for magmatism in suppression of post-extinction biotic recovery.National Science Foundation (U.S.) (Continental Dynamics Grant EAR-0807475)National Science Foundation (U.S.) (Instrumentation and Facilities Grant EAR-0931839

Electron Microprobe Chemical Dating of Uraninite as a Reconnaissance Tool for Leucogranite Geochronology

We suggest that electron microprobe techniques may be employed to date Tertiary samples of uraninite (UO~2~), which can contain very high concentrations of radiogenic Pb after only a few million of years of U and Th decay. Although uraninite is regarded as a rare accessory mineral, it is relatively abundant in leucogranitic rocks such as those found in the Himalayan orogen. We apply the U-Th-total Pb electron microprobe chemical dating method to a uraninite crystal from a ca. 18.3 Ma dike of the Mugu granite from the Upper Mustang region of central Nepal. With this technique, we calculate a mean chemical date that is consistent with isotope-dilution thermal ionization mass spectrometry (ID-TIMS) U-Pb dates obtained from seven other uraninite grains and a monazite crystal from the same sample. Electron microprobe chemical dating yields results that typically will be an order of magnitude less precise than conventional dates: in the specific case of the Mugu granite, single point chemical dates each have ca. 1.5 Ma 2[sigma] (95%) confidence level uncertainties. However, the mean chemical date of 15 point analyses of the crystal we study has a 2SE (2 standard error) uncertainty of ca. 400 ka, comparable to uncertainties obtained with ID-TIMS. These results show that electron microprobe chemical dating of uraninite has substantial promise as a reconnaissance tool for the geochronology of young granitic rocks. The electron microprobe work also reveals substantial chemical complexity within uraninite that must be taken into account. The analyzed crystal displays a texturally and chemically distinctive core and rim that suggests episodic growth. Concentration gradients in U, Th, and Y across the boundary imply diffusive modification. We estimate the diffusivity of U, Th, and Y in uraninite at ca. 700 °C to be > 10-7 cm2 s-1. In contrast, Pb shows no distinctive concentration gradient across the core-rim boundary, implying that Pb has a much higher diffusivity in uraninite than U, Th, or Y. We estimate that Pb loss of as much as ca. 8.9% has occurred in the uraninite grains we analyzed by ID-TIMS

Deep crustal anatexis, magma mixing, and the generation of epizonal plutons in the Southern Rocky Mountains, Colorado

The Never Summer Mountains in north-central Colorado, USA, are cored by two Oligocene, epizonal granitic plutons originally emplaced in the shallow levels of a short-lived (~1 m.y.), small-volume continental magmatic system. The younger Mt. Cumulus stock (28.015 ± 0.012 Ma) is a syenogranite equivalent compositionally to topaz rhyolites. A comparison to the chemical and isotopic composition of crustal xenoliths entrained in nearby Devonian kimberlites demonstrates that the silicic melts parental to the stock were likely derived from anatexis of local Paleoproterozoic, garnet-absent, mafic lower continental crust. In contrast, the older Mt. Richthofen stock is compositionally heterogeneous and ranges from monzodiorite to monzogranite. Major and trace element abundances and Sr, Nd and Pb isotopic ratios in this stock vary regularly with increasing whole rock wt% SiO2. These data suggest that the Mt. Richthofen stock was constructed from mixed mafic and felsic magmas, the former corresponding to lithosphere-derived basaltic magmas similar isotopically to mafic enclaves entrained in the eastern portions of the stock and the latter corresponding to less differentiated versions of the silicic melts parental to the Mt. Cumulus stock. Zircon U–Pb geochronology further reveals that the Mt. Richthofen stock was incrementally emplaced over a time interval from at least 28.975 ± 0.020 to 28.742 ± 0.053 Ma. Magma mixing could have occurred either in situ in the upper crust during basaltic underplating and remelting of an antecedent, incrementally emplaced, silicic intrusive body, or at depth in the lower crust prior to periodic magma ascent and emplacement in the shallow crust. Overall, the two stocks demonstrate that magmatism associated with the Never Summer igneous complex was fundamentally bimodal in composition. Highly silicic anatectic melts of the mafic lower crust and basaltic, mantle-derived magmas were the primary melts in the magma system, with mixing of the two producing intermediate composition magmas such as those from which Mt. Richthofen stock was constructed.National Science Foundation (U.S.) (Grant EAR-0931839

A strategy for cross-calibrating U–Pb chronology and astrochronology of sedimentary sequences: An example from the Green River Formation, Wyoming, USA

Astronomical calibration of the geological timescale has been limited until recently by the precision and accuracy of radioisotopic dates, especially for pre-Neogene records. Uncertainties for radioisotopic dates of older strata were typically much larger than a single precessional cycle, and dates were often sparse, leading to the practice of orbital tuning of cyclic strata in order to astronomically calibrate the desired interval. Ideally, in order to test the assumptions of astronomical calibration with geochronology, it is necessary that the precision of radioisotopic dates be comparable to the period of the cycle being tested. The new U–Pb CA-TIMS (chemical abrasion–thermal ionization mass spectrometry) zircon dates reported here conform to this precision requirement, with 2σ analytical uncertainties from ±11000 to ±52 000 years for seven volcanic ashes from the Wilkins Peak Member of the Green River Formation. The zircon dates have simple distributions with few outliers and allow accurate estimations of the eruption ages with potential inaccuracies of less than precessional cycle. The Eocene Green River Formation (Wyoming, USA) has long been recognized as a record of cyclicly- deposited lacustrine sediments, and the abundant intercalated volcanic ashes make it a suitable place to test new approaches to astronomical calibration of cyclic strata. The abundance of different types of marker beds, including tuffs that are intercalated with the sedimentary cycles, guarantee an unambiguous correlation between sampling locations of dated tuffs on the margins of the basin and the basin center where the cyclicity is best developed, thus reducing any stratigraphic uncertainties to a fraction of (hypothesized) precession cycle. Tuning-based orbital age models, accepted by the previous geochronology, significantly deviate from the new geochronology, whereas a previously rejected model that assumes a short eccentricity period of 125 ky is now allowed. In order to test possible explanations for the apparent 125 ky period, such as changes in orbital periods, or gaps in the sedimentary record, we present an iterative strategy to select future ashes for dating such that the astronomical calibration/testing is optimized. We iteratively contrast two ad-hoc age models that bracket the linear interpolation between the dated ashes. The optimal intervals for further dating are located where the deviations between the models exceed our reported uncertainties. We propose that the iterative approach described here should become the standard for establishing a rigorous orbital calibration of the stratigraphic record where sufficient ashes exist

Isotopic composition ( 238 U/ 235 U) of some commonly used uranium reference materials

Abstract We have determined 238 U/ 235 U ratios for a suite of commonly used natural (CRM 112a, SRM 950a, and HU-1) and synthetic (IRMM 184 and CRM U500) uranium reference materials by thermal ionisation mass-spectrometry (TIMS) using the IRMM 3636 233 U-236 U double spike to accurately correct for mass fractionation. Total uncertainty on the 238 U/ 235 U determinations is estimated to be <0.02% (2r). These natural 238 U/ 235 U values are different from the widely used 'consensus' value (137.88), with each standard having lower 238 U/ 235 U values by up to 0.08%. The 238 U/ 235 U ratio determined for CRM U500 and IRMM 184 are within error of their certified values; however, the total uncertainty for CRM U500 is substantially reduced (from 0.1% to 0.02%). These reference materials are commonly used to assess mass-spectrometer performance and accuracy, calibrate isotope tracers employed in U, U-Th and U-Pb isotopic studies, and as a reference for terrestrial and meteoritic 238 U/ 235 U variations. These new 238 U/ 235 U values will thus provide greater accuracy and reduced uncertainty for a wide variety of isotopic determinations

Evaluating uncertainties in the calibration of isotopic reference materials and multi-element isotopic tracers (EARTHTIME Tracer Calibration Part II)

A statistical approach to evaluating uncertainties in the calibration of multi-element isotopic tracers has been developed and applied to determining the isotopic composition of mixed U-Pb (202Pb-205Pb-233U-235U) tracers used for accurate isotope dilution U-Pb geochronology. Our experiment, part of the EARTHTIME initiative, directly links the tracer calibration to first-principles measurements of mass and purity that are all traceable to SI units, thereby quantifying the accuracy and precision of U-Pb dates in absolute time. The calibration incorporates new more accurate and precise purity measurements for a number of commonly used Pb and U reference materials, and requires inter-relating their isotopic compositions and uncertainties. Similar methods can be used for other isotope systems that utilize multiple isotopic standards for calibration purposes. We also detail the inter-calibration of three publicly available U-Pb gravimetric solutions, which can be used to bring the same first-principles traceability to in-house U-Pb tracers from other laboratories. Accounting for uncertainty correlations in the tracer isotope ratios yields a tracer calibration contribution to the relative uncertainty of a 206Pb/238U date that is only half of the relative uncertainty in the 235U/205Pb ratio of the tracer, which was historically used to approximate the tracer related uncertainty contribution to 206Pb/238U dates. The tracer uncertainty contribution to 206Pb/238U dates has in this way been reduced to <300 ppm when using the EARTHTIME and similarly calibrated tracers

Zircon U-Pb Geochronology Links the End-Triassic Extinction with the Central Atlantic Magmatic Province

The end-Triassic extinction is characterized by major losses in both terrestrial and marine diversity, setting the stage for dinosaurs to dominate Earth for the next 136 million years. Despite the approximate coincidence between this extinction and flood basalt volcanism, existing geochronologic dates have insufficient resolution to confirm eruptive rates required to induce major climate perturbations. Here, we present new zircon uranium-lead (U-Pb) geochronologic constraints on the age and duration of flood basalt volcanism within the Central Atlantic Magmatic Province. This chronology demonstrates synchroneity between the earliest volcanism and extinction, tests and corroborates the existing astrochronologic time scale, and shows that the release of magma and associated atmospheric flux occurred in four pulses over about 600,000 years, indicating expansive volcanism even as the biologic recovery was under way

Isotopic composition (238U/235U) of some commonly used uranium reference materials

We have determined 238U/235U ratios for a suite of commonly used natural (CRM 112a, SRM 950a, and HU-1) and synthetic (IRMM 184 and CRM U500) uranium reference materials by thermal ionisation mass-spectrometry (TIMS) using the IRMM 3636 233U-236U double spike to accurately correct for mass fractionation. Total uncertainty on the 238U/235U determinations is estimated to be < 0.02% (2σ). These natural 238U/235U values are different from the widely used ‘consensus’ value (137.88), with each standard having lower 238U/235U values by up to 0.08%. The 238U/235U ratio determined for CRM U500 and IRMM 184 are within error of their certified values; however, the total uncertainty for CRM U500 is substantially reduced (from 0.1% to 0.02%). These reference materials are commonly used to assess mass spectrometer performance and accuracy, calibrate isotope tracers employed in U, U-Th and U-Pb isotopic studies, and as a reference for terrestrial and meteoritic 238U/235U variations. These new 238U/235U values will thus provide greater accuracy and reduced uncertainty for a wide variety of isotopic determinations

U-Pb dating of interspersed gabbroic magmatism and hydrothermal metamorphism during lower crustal accretion, Vema lithospheric section, Mid-Atlantic Ridge

New U/Pb analyses of zircon and xenotime constrain the timing of magmatism, magmatic assimilation, and hydrothermal metamorphism during formation of the lower crust at the Mid-Atlantic Ridge. The studied sample is an altered gabbro from the Vema lithospheric section (11°N). Primary gabbroic minerals have been almost completely replaced by multiple hydrothermal overprints: cummingtonitic amphibole and albite formed during high-temperature hydration reactions and are overgrown first by kerolite and then prehnite and chlorite. In a previous study, clear inclusion-free zircons from the sample yielded Th-corrected 206Pb/238U dates of 13.528 ± 0.101 to 13.353 ± 0.057 Ma. Ti concentrations, reported here, zoning patterns and calculated Th/U of the dated grains are consistent with these zircons having grown during igneous crystallization. To determine the timing of hydrothermal metamorphism, we dated a second population of zircons, with ubiquitous <1–20 µm chlorite inclusions, and xenotimes that postdate formation of metamorphic albite. The textures and inclusions of the inclusion-rich zircons suggest that they formed by coupled dissolution-reprecipitation of metastable igneous zircon during or following hydrothermal metamorphism. Th-corrected 206Pb/238U dates for the inclusion-rich zircons range from 13.598 ± 0.012 to 13.503 ± 0.018 Ma and predate crystallization of all but one of the inclusion-free zircons, suggesting that the inclusion-rich zircons were assimilated from older hydrothermally altered wall rocks. The xenotime dates are sensitive to the Th correction applied, but even using a maximum correction, 206Pb/238U dates range from 13.341 ± 0.162 to 12.993 ± 0.055 Ma and postdate crystallization of both the inclusion-rich zircons and inclusion-free igneous zircons, reflecting a second hydrothermal event. The data provide evidence for alternating magmatism and hydrothermal metamorphism at or near the ridge axis during accretion of the lower crust at a ridge-transform intersection and suggest that hydrothermally altered crust was assimilated into younger gabbroic magmas. The results of this study show that high-precision U-Pb dating is a powerful method for studying the timing of magmatic and hydrothermal processes at mid-ocean ridges