Geology topics

Matthew A. Coble

Publications and source records attributed to Matthew A. Coble.

7 recordsLinked to original sources

USGS2019

Ten-million years of activity within the Eastern California Shear Zone from U-Pb dating of fault-zone opal

Reconstructions of long-term fault activity are essential for understanding both the mechanisms controlling fault behavior and accurate earthquake hazard assessments. Increasing evidence for temporal variations in strain accumulation suggests non-uniform strain rates over a range of historic to geologic timescales. The paucity of long-term records of fault activity has limited our ability to resolve these variations. We present a method for constraining long-term fault activity based on U-Pb dating of fault-related opal from secondary fault segments within the Eastern California Shear Zone (ECSZ). The presence of sheared and breccia-cemented opaline silica within well-exposed faults at near-surface conditions suggest that opal formation is associated with high-magnitude earthquakes capable of surface rupture (>6 M). Temporal constraints from sheared syntectonic opal (n=74) on related secondary faults from this study provide new insights on the timing of fault initiation, reactivation, and longevity. The oldest dates obtained indicate that ECSZ activity commenced at or before 10 Ma. Multiple deformation events dated within a single structure on episodically deposited and sheared opal (up to six generations), demonstrate that fault reactivation occurred over 105 year timescales (0.7-0.1 Ma). Relative probabilities of dated deformation events can be used to evaluate changes in fault activity in the past 2.5 Ma (n=60). This analysis indicates enhanced fault activity starting at 2 Ma and peaking around 1 Ma, possibly due to fault-interactions and distribution of deformation between the ECSZ and the San Andreas Fault.

California↗

USGS2018

GHR1 Zircon – A new Eocene natural reference material for microbeam U-Pb geochronology and Hf isotopic analysis of zircon

We present multitechnique U-Pb geochronology and Hf isotopic data from zircon separated from rapakivi biotite granite within the Eocene Golden Horn batholith in Washington, USA. A weighted mean of twenty-five Th-corrected 206 Pb/ 238 U zircon dates produced at two independent laboratories using chemical abrasion-isotope dilution-thermal ionisation mass spectrometry (CA-ID-TIMS) is 48.106 ± 0.023 Ma (2 s analytical including tracer uncertainties, MSWD = 1.53) and is our recommended date for GHR1 zircon. Microbeam 206 Pb/ 238 U dates from laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and secondary ion mass spectrometry (SIMS) laboratories are reproducible and in agreement with the CA-ID-TIMS date to within < 1.5%. Solution multi-collector ICP-MS (MC-ICP-MS) measurements of Hf isotopes from chemically purified aliquots of GHR1 yield a mean 176 Hf/ 177 Hf of 0.283050 ± 17 (2 s , n = 10), corresponding to a εHf 0 of +9.3. Hafnium isotopic measurements from two LA-ICP-MS laboratories are in agreement with the solution MC-ICP-MS value. The reproducibility of 206 Pb/ 238 U and 176 Hf/ 177 Hf ratios from GHR1 zircon across a variety of measurement techniques demonstrates their homogeneity in most grains. Additionally, the effectively limitless reserves of GHR1 material from an accessible exposure suggest that GHR1 can provide a useful reference material for U-Pb geochronology of Cenozoic zircon and Hf isotopic measurements of zircon with radiogenic 176 Hf/ 177 Hf.

Geostandards and Geoanalytical Research↗

USGS2018

Trace element characterisation of MAD‐559 zircon reference material for ion microprobe analysis

We document the composition of a natural zircon gemstone sourced from Madagascar, MAD‐559 – a new reference material for calibrating trace element mass fractions in zircon measured by SIMS. The composition of MAD‐559 was quantified by calibration relative to the well‐documented zircon reference material 91500, for which we compiled existing published data (Mg, Al, Y, rare earth elements, Hf, U, Th) and performed new measurements to characterise the mass fraction of less commonly measured elements (Li, Be, B, F, Na, P, K, Ca, Sc, Ti, Fe, Nb). Measurement results of SL13, CZ3 and MAD‐1 zircons and NIST SRM glasses were performed as quality control materials to test measurement bias and repeatability. We show the intermediate precision for most trace element measurement results of MAD‐559 to be between ± 3% and ± 5% RSD based on 139 measurements by SIMS on twenty‐five individual polished zircon chips measured during a 24‐h period, as well as repeat measurements performed over five separate analytical sessions. Trace element mass fractions were also measured by LA‐ICP‐MS in two different laboratories, and major element compositions measured by electron microprobe, to compare with results measured by SIMS. Based on laser Raman and hyperspectral cathodoluminescence spectroscopy, we show MAD‐559 to have high crystal disorder due to radiation damage relative to crystalline zircon (e.g., SL13 and 91500 zircon). Although the high cumulative alpha dose of MAD‐559 zircon makes it a poor reference material for geochronology, the consistency of the trace element mass fraction results measured in multiple sessions and by various measurement methods shows that it is an ideal reference material for microanalytical trace element mass fraction quantification of zircon.

Geostandards and Geoanalytical Research↗

USGS2017

New zircon (U-Th)/He and U/Pb eruption age for the Rockland tephra, western USA

Eruption ages of a number of prominent Quaternary volcanic deposits remain inaccurately and/or imprecisely constrained, despite their importance as regional stratigraphic markers in paleo-environment reconstruction and as evidence of climate-altering eruptions. Accurately dating volcanic deposits presents challenging analytical considerations, including poor radiogenic yield, scarcity of datable minerals, and contamination of crystal populations by magma, eruption, and transport processes. One prominent example is the Rockland tephra, which erupted from the Lassen Volcanic Center in the southern Cascade arc. Despite a range in published eruption ages from 0.40 to 0.63 Ma, the Rockland tephra is extensively used as a marker bed across the western United States. To more accurately and precisely constrain the age of the Rockland tephra-producing eruption, we report U/Pb crystallization dates from the outermost ∼2 μm of zircon crystal faces (surfaces) using secondary ion mass spectrometry (SIMS). Our new weighted mean 238 U/ 206 Pb age for Rockland tephra zircon surfaces is 0.598 ± 0.013 Ma (2σ) and MSWD = 1.11 (mean square weighted deviation). As an independent test of the accuracy of this age, we obtained new (U-Th)/He dates from individual zircon grains from the Rockland tephra, which yielded a weighted mean age of 0.599 ± 0.012 Ma (2σ, MSWD = 5.13). We also obtained a (U-Th)/He age of 0.628 ± 0.014 Ma (MSWD = 1.19) for the Lava Creek Tuff member B, which was analyzed as a secondary standard to test the accuracy of the (U-Th)/He technique for Quaternary tephras, and to evaluate assumptions made in the model-age calculation. Concordance of new U/Pb and (U-Th)/He zircon ages reinforces the accuracy of our preferred Rockland tephra eruption age, and confirms that zircon surface dates sample zircon growth up to the time of eruption. We demonstrate the broad applicability of coupled U/Pb zircon-surface and single-grain zircon (U-Th)/He geochronology to accurate dating of Quaternary tephra, and highlight the challenges and opportunities of this technique.

Quaternary Science Reviews↗

USGS2016

Refined depositional history and dating of the Tongaporutuan reference section, north Taranaki, New Zealand: new volcanic ash U-Pb zircon ages, biostratigraphy and sedimentation rates

This study presents new radiometric ages from volcanic ash beds within a c. 1900 m thick, progradational, deep-water clastic slope succession of late Miocene age exposed along the north Taranaki coast of the North Island, New Zealand. The ash beds yield U–Pb zircon ages ranging from 10.63 ± 0.65 Ma to 8.97 ± 0.22 Ma. The new ages are compatible with and provide corroboration of New Zealand Tongaporutuan Stage planktic foraminiferal and bolboformid biostratigraphic events identified in the same section. The close accord between these two age datasets provides a stratigraphically consistent and coherent basis for examining margin evolution. The arrival of a prograding clastic wedge and ensuing upward shoaling is recorded by sedimentation rates c. 2000 m/Ma–1 that are an order of magnitude higher than sedimentation rates on the precursor deep basin floor. This outcrop study provides new constraints for interpreting analogous subsurface deposits in Taranaki Basin and complements the regional late Miocene biostratigraphic dating framework.

Taranaki↗

USGS2016

Chemical abrasion-SIMS (CA-SIMS) U-Pb dating of zircon from the late Eocene Caetano caldera, Nevada

Zircon geochronology is a critical tool for establishing geologic ages and time scales of processes in the Earth's crust. However, for zircons compromised by open system behavior, achieving robust dates can be difficult. Chemical abrasion (CA) is a routine step prior to thermal ionization mass spectrometry (TIMS) dating of zircon to remove radiation-damaged parts of grains that may have experienced open system behavior and loss of radiogenic Pb. While this technique has been shown to improve the accuracy and precision of TIMS dating, its application to high-spatial resolution dating methods, such as secondary ion mass spectrometry (SIMS), is relatively uncommon. In our efforts to U-Pb date zircons from the late Eocene Caetano caldera by SIMS (SHRIMP-RG: sensitive high resolution ion microprobe, reverse geometry), some grains yielded anomalously young U-Pb ages that implicated Pb-loss and motivated us to investigate with a comparative CA and non-CA dating study. We present CA and non-CA 206 Pb/ 238 U ages and trace elements determined by SHRIMP-RG for zircons from three Caetano samples (Caetano Tuff, Redrock Canyon porphyry, and a silicic ring-fracture intrusion) and for R33 and TEMORA-2 reference zircons. We find that non-CA Caetano zircons have weighted mean or bimodal U-Pb ages that are 2–4% younger than CA zircons for the same samples. CA Caetano zircons have mean U-Pb ages that are 0.4–0.6 Myr older than the 40 Ar/ 39 Ar sanidine eruption age (34.00 ± 0.03 Ma; error-weighted mean, 2σ), whereas non-CA zircons have ages that are 0.7–1.3 Myr younger. U-Pb ages do not correlate with U (~ 100–800 ppm), Th (~ 50–300 ppm) or any other measured zircon trace elements (Y, Hf, REE), and CA and non-CA Caetano zircons define identical trace element ranges. No statistically significant difference in U-Pb age is observed for CA versus non-CA R33 or TEMORA-2 zircons. Optical profiler measurements of ion microprobe pits demonstrate consistent depths of ~ 1.6 μm for CA and non-CA Caetano, R33 and TEMORA-2 zircons, and do not indicate variations in secondary ion sputtering rates due to chemical or structural changes from the CA treatment. Our new data underscore the potential for cryptic Pb-loss to go unrecognized in other geologically young magmatic centers that do not have zircons with high U, statistically discordant isotope ratios, high common Pb, or metamict textures.

Nevada↗

USGS2012

The Stanford-U.S. Geological Survey SHRIMP ion microprobe--a tool for micro-scale chemical and isotopic analysis

Answers to many questions in Earth science require chemical analysis of minute volumes of minerals, volcanic glass, or biological materials. Secondary Ion Mass Spectrometry (SIMS) is an extremely sensitive analytical method in which a 5–30 micrometer diameter "primary" beam of charged particles (ions) is focused on a region of a solid specimen to sputter secondary ions from 1–5 nanograms of the sample under high vacuum. The elemental abundances and isotopic ratios of these secondary ions are determined with a mass spectrometer. These results can be used for geochronology to determine the age of a region within a crystal thousands to billions of years old or to precisely measure trace abundances of chemical elements at concentrations as low as parts per billion. A partnership of the U.S. Geological Survey and the Stanford University School of Earth Sciences operates a large SIMS instrument, the Sensitive High-Resolution Ion Microprobe with Reverse Geometry (SHRIMP–RG) on the Stanford campus.

Fact Sheet↗