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At least 415 records · Page 23Linked to original sources

USGS2004

Emplacement mechanisms of the South Kona slide complex, Hawaii Island: Sampling and observations by remotely operated vehicle Kaiko

Emplacement of a giant submarine slide complex, offshore of South Kona, Hawaii Island, was investigated in 2001 by visual observation and in-situ sampling on the bench scarp and a megablock, during two dives utilizing the Remotely Operated Vehicle (ROV) Kaiko and its mother ship R/V Kairei. Topography of the bench scarp and megablocks were defined in 3-D perspective, using high-resolution digital bathymetric data acquired during the cruise. Compositions of 34 rock samples provide constraints on the landslide source regions and emplacement mechanisms. The bench scarp consists mainly of highly fractured, vesiculated, and oxidized a-a lavas that slumped from the subaerial flank of ancestral Mauna Loa. The megablock contains three units: block facies, matrix facies, and draped sediment. The block facies contains hyaloclastite interbedded with massive lava, which slid from the shallow submarine flank of ancestral Mauna Loa, as indicated by glassy groundmass of the hyaloclastite, low oxidation state, and low sulfur content. The matrix facies, which directly overlies the block facies and is similar to a lahar deposit, is thought to have been deposited from the water column immediately after the South Kona slide event. The draped sediment is a thin high-density turbidite layer that may be a distal facies of the Alika-2 debris-avalanche deposit; its composition overlaps with rocks from subaerial Mauna Loa. The deposits generated by the South Kona slide vary from debris avalanche deposit to turbidite. Spatial distribution of the deposits is consistent with deposits related to large landslides adjacent to other Hawaiian volcanoes and the Canary Islands. ?? Springer-Verlag 2004.

Bulletin of Volcanology↗

USGS2016

Dimmuborgir: a rootless shield complex in northern Iceland

The origin of Dimmuborgir, a shield-like volcanic structure within the Younger Laxá lava flow field near Lake Mývatn, in northern Iceland, has long been questioned. New airborne laser mapping (light detection and ranging (LiDAR)), combined with ground-penetrating radar results and a detailed field study, suggests that Dimmuborgir is a complex of at least two overlapping rootless shields fed by lava erupting from the nearby Lúdentarborgir crater row. This model builds upon previous explanations for the formation of Dimmuborgir and is consistent with observations of rootless shield development at Kīlauea Volcano, Hawaii. The larger rootless shields at Dimmuborgir, 1–1.5 km in diameter, elliptical in plan view, &sim;30 m in height, and each with a 500-m-wide summit depression, were capable of storing as much as 2–3 × 10 6 m 3 of lava. They were fed by lava which descended 30–60 m in lava tubes along a distance of 3 km from the crater row. The height difference generated pressure sufficient to build rootless shields at Dimmuborgir in a timescale of weeks. The main summit depressions, inferred to be drained lava ponds, could have emptied via a 30-m-wide × 5-m-deep channel, with estimated effusion rates of 0.7–7 m 3 s −1 and minimum flow durations of 5–50 days. We argue that the pillars for which Dimmuborgir is famed are remnants of lava pond rims, at various stages of disintegration that formed during pond drainage.

Bulletin of Volcanology↗

USGS2012

Using hydrogeochemical methods to evaluate complex quaternary subsurface stratigraphy Block Island, Rhode Island, USA

One of the major problems in hydrogeologic investigations of glaciated regions is the determination of complex stratigraphic relationships in the subsurface where insufficient information is available from drilling and geophysical records. In this paper, chemical characteristics of groundwater were used to identify stratigraphic changes in glacial deposits that were previously inferred on Block Island, Rhode Island, USA, an emergent remnant of the late Wisconsinan terminal moraine, located approximately 16 km south of the Rhode Island mainland. Two chemically distinct water types are recognized on the island: 1) high-iron, characterized by dissolved silica levels in excess of 20 mg/L, bicarbonate greater than 30 mg/L and dissolved iron ranging from 1-20 mg/L; and 2) low-iron, characterized by dissolved silica levels below 16 mg/L, bicarbonate less than 30 mg/L, and less than 0.3 mg/L dissolved iron. The spatial distribution of iron-bearing minerals and organic matter and the resulting redox conditions are believed to control the occurrence of highiron groundwater. The high-iron waters occur almost exclusively in the eastern half of the island and appear to coincide with the presence of allochthonous blocks of Cretaceous-age coastal-plain sediments that were incorporated into Pleistocene-age deposits derived from the Narragansett Bay-Buzzard's Bay lobe of the Late Wisconsinan Laurentide ice sheet. The low-iron waters occur in the western half of the island, where the occurrence of these Cretaceous-age blocks is rare and the sediments are attributed to a sublobe of the Hudson-Champlain lobe of the Late Wisconsinan ice sheet.

Rhode Island↗

USGS2020

Complex patterns of genetic and morphological differentiation in the Smallmouth Bass subspecies (Micropterus dolomieu dolomieu and M. d. velox) of the Central Interior Highlands

Due to geologic processes and recent anthropogenic introductions, patterns of genetic and morphological diversity within the Smallmouth Bass ( Micropterus dolomieu ), which are endemic to the central and eastern United States (USA), are poorly understood. We assessed genetic and morphological differentiation between the widespread Northern Smallmouth Bass ( M. d. dolomieu ) and the more restricted Neosho Smallmouth Bass ( M. d. velox ) where their ranges meet in the Central Interior Highlands ecoregion (CIH). Data from 14 microsatellite loci were used to conduct S TRUCTURE and principal components analyses to evaluate diversity across populations and screen for hybridization with sympatric Spotted Bass ( M. punctulatus ). We also tested for morphological differences using five morphometric traits and one meristic trait. We found support for three genetic clusters corresponding to previously described taxonomic variation; five clusters largely corresponding to river systems; and nine clusters representing hierarchical population structure within both ranges. We found evidence of a unique genetic cluster in tributaries of the White River within the Northern Smallmouth Bass range and admixture between the subspecies throughout the Neosho range. We also found evidence of morphological differentiation between subspecies; Neosho Smallmouth Bass exhibited larger head length than Northern Smallmouth Bass relative to total length, and there was a significant interaction of subspecies and orbital length, possibly indicating differential growth patterns between subspecies. Our results reveal multiple levels of divergence, suggesting the CIH harbors greater and more complex Smallmouth Bass diversity than previously thought.

Arkansas, Illinois, Kansas, Mississippi, Missouri,↗

USGS2023

Revisiting conservation units for the endangered mountain yellow-legged frog species complex (Rana muscosa, Rana sierrae) using multiple genomic methods

Insights from conservation genomics have dramatically improved recovery plans for numerous endangered species. However, most taxa have yet to benefit from the full application of genomic technologies. The mountain yellow-legged frog species complex, Rana muscosa and Rana sierrae, inhabits the Sierra Nevada mountains and Transverse/Peninsular Ranges of California and Nevada. Both species have declined precipitously throughout their historical distributions. Conservation management plans outline extensive ongoing recovery efforts but are still based on the genetic structure determined primarily using a single mitochondrial sequence. Our study used two different sequencing strategies – amplicon sequencing and exome capture – to refine our understanding of the population genetics of these imperiled amphibians. We used buccal swabs, museum tissue samples, and archived skin swabs to genotype frog populations across their range. Using the amplicon sequencing and exome capture datasets separately and combined, we document five major genetic clusters. Notably, we found evidence supporting previous species boundaries within Kings Canyon National Park with some exceptions at individual sites. Though we see evidence of genetic clustering, especially in the R. muscosa clade, we also found evidence of some admixture across cluster boundaries in the R. sierrae clade, suggesting a stepping-stone model of population structure. We also find that the southern R. muscosa cluster had large runs of homozygosity and the lowest overall heterozygosity of any of the clusters, consistent with previous reports of marked declines in this area. Overall, our results clarify management unit designations across the range of an endangered species and highlight the importance of sampling the entire range of a species, even when collecting genome-scale data.

California↗

USGS2011

CDFISH: an individual-based, spatially-explicit, landscape genetics simulator for aquatic species in complex riverscapes

We introduce Cost Distance FISHeries (CDFISH), a simulator of population genetics and connectivity in complex riverscapes for a wide range of environmental scenarios of aquatic organisms. The spatially-explicit program implements individual-based genetic modeling with Mendelian inheritance and k -allele mutation on a riverscape with resistance to movement. The program simulates individuals in subpopulations through time employing user-defined functions of individual migration, reproduction, mortality, and dispersal through straying on a continuous resistance surface.

Conservation Genetics Resources↗

USGS1976

Carbon, hydrogen, and oxygen isotope studies of the regional metamorphic complex at Naxos, Greece

At Naxos, Greece, a migmatite dome is surrounded by schists and marbles of decreasing metamorphic grade. Sillimanite, kyanite, biotite, chlorite, and glaucophane zones are recognized at successively greater distances from the migmatite dome. Quartz-muscovite and quartz-biotite oxygen isotope and mineralogie temperatures range from 350 to 700°C. The metamorphic complex can be divided into multiple schist-rich (including migmatites) and marblerich zones. The δ 18 O values of silicate minerals in migmatite and schist units and quartz segregations in the schist-rich zones decrease with increase in metamorphic grades. The calculated δ 18 O H2O values of the metamorphic fluids in the schist-rich zones decrease from about 15‰ in the lower grades to an average of about 8.5‰ in the migmatite. The δD values of OH-minerals (muscovite, biotite, chlorite, and glaucophane) in the schist-rich zones also decrease with increase in grade. The calculated δD H2O values for the metamorphic fluid decrease from −5‰ in the glaucophane zone to an average of about −70‰ in the migmatite. The δD values of water in fluid inclusions in quartz segregations in the higher grade rocks are consistent with this trend. Theδ 18 O values of silicate minerals and quartz segregations in marble-rich zones are usually very large and were controlled by exchange with the adjacent marbles. The δD values of the OH minerals in some marble-rich zones may reflect the value of water contained in the rocks prior to metamorphism. Detailed data on 20 marble units show systematic variations of δ 18 O values which depend upon metamorphic grade. Below the 540°C isograd very steep δ 18 O gradients at the margins and large δ 18 O values in the interior of the marbles indicate that oxygen isotope exchange with the adjacent schist units was usually limited to the margins of the marbles with more exchange occurring in the stratigraphic bottom than in the top margins. Above the 540°C isograd lower δ 18 O values occur in the interior of the marble units reflecting a greater degree of recrystallization and the occurrence of Ca-Mg-silicates. Almost all the δ 13 C values of the marbles are in the range of unaltered marine limestones. Nevertheless, the δ 13 C values of most marble units show a general correlation with δ 18 O values. The CO 2 H 2 O "> CO 2 H 2 O mole ratio of fluid inclusions in quartz segregations range from 0.01 to 2. Theδ 13 C values of the CO 2 range from −8.0 to 3.6‰ and indicate that at some localities CO 2 in the metamorphic fluid was not in carbon isotopic equilibrium with the marbles.

Geochimica et Cosmochimica Acta↗

USGS1993

Determination of size and element composition distributions of complex colloids by sedimentation field-flow fractionation—inductively coupled plasma mass spectrometry

Sedimentation field-flow fractionation (SdFFF) and inductively coupled plasma mass spectrometry (ICP-MS) have been directly combined and the resulting SdFFF-ICP-MS instrument can be used to produce element based size distributions of colloidal samples. Using appropriate tracer elements the size distributions of specific components can be picked out from a complex mixture. Changes in chemical composition of mixtures as a function of particle size can be readily monitored by plotting appropriate element atomic ratio distributions. These applications have been illustrated using data obtained with samples of the clay minerals kaolinite and illite and a natural suspended particulate matter from the Darling River (Australia).

Journal of Chromatography A↗

USGS1984

Preliminary results, Central Gneiss Complex of the Coast Range batholith, southeastern Alaska: the roots of a high-K, calc-alkaline arc?

The Central Gneiss Complex (CGC) of the Coast Range batholith is the oldest unit of the batholith east of Ketchikan, Alaska, being dated by the zircon UPb method (by T.W. Stern) at 128-140 Ma. Heterogeneous, layered, commonly migmatitic, orthogneiss of hornblende-biotite quartz diorite, tonalite, quartz monzodiorite and granodiorite compositions (IUGS terminology) form the major part of the CGC. These gneisses show a range of 50-65% SiO2 and are high in Al2O3 (c. 15-19%), K2O (1.5-4%) and Sr (800-900 ppm). Most major elements show coherent, typically magmatic trends with SiO2. La and Rb show maxima at ??? 58% SiO2. Initial 87Sr/86Sr ratios are relatively high and range from 0.7052 to 0.7066. Wallrocks of the CGC are mostly metagraywacke, pelite and metavolcanic rocks at amphibolite facies; they are geochemically dissimilar to the CGC. Major and minor elements of the CGC are very similar to those of high-K orogenic, calc-alkaline andesitic suites. The CGC may have formed largely by fractionation of mantle-derived, high AlKSr basaltic liquid in an ascending diapir, having hornblende, plagioclase, and biotite as major precipitating phases. The CGC probably represents the plutonic equivalent of a continental-margin or Andean arc that formed when the Taku terrane of the Insular belt on the west collided with the previously emplaced (but also allochthonous) Stikine terrane on the east in Late Jurassic or Early Cretaceous time. ?? 1984.

Physics of the Earth and Planetary Interiors↗

USGS1978

Distribution and character of upper Mesozoic subduction complexes along the west coast of North America

Structurally complex sequences of sedimentary, volcanic, and intrusive igneous rocks characterize a nearly continuous narrow band along the Pacific coast of North America from Baja California, Mexico to southern Alaska. They occur in two modes: (1) as complexly folded but coherent sequences of graywacke and argillite that locally exhibit blueschist-grade metamorphism, and (2) as melanges containing large blocks of graywacke, chert, volcanic and plutonic rocks, high-grade schist, and limestone in a highly sheared pelitic, cherty, or sandstone matrix. Fossils from the coherent graywacke sequences range in age from late Jurassic to Eocene; fossils from limestone blocks in the melanges range in age from mid-Paleozoic to middle Cretaceous. Fossils from the matrix surrounding the blocks, however, are of Jurassic, Cretaceous, and rarely, Tertiary age, indicating that fossils from the blocks cannot be used to date the time of formation of the melanges. Both the deformation of the graywacke, with accompanying blueschist metamorphism, as well as the formation of the melanges, are believed to be the result of late Mesozoic and early Tertiary subduction. The origin of the melanges, particularly the emplacement of exotic tectonic blocks, is not understood.

Alaska, California, Oregon, Washington↗

USGS1996

Rainbow trout embryotoxicity of a complex contaminant mixture extracted from Lake Michigan lake trout

Persistent Hydrophobic contaminants such as poly chlorinated dibenzo- p -dioxins, dibenzofurans and biphenyl congeners are present in aquatic systems, and are known to produce adverse effects in fish. Reproductive failure in fish populations has been observed in aquatic systems contaminated with persistent hydrophobic compounds. In order to mimic maternal transfer of environmental contaminants to newly fertilized fish eggs, a complex environmental extract was tested for embryotoxicity in a nanoinjection bioassay with embryos of rainbow trout. The extract was obtained from whole adult lake trout collected from Lake Michigan in 1988. The tissue extraction involved blending and dehydration with sodium sulfate, column extraction, dialysis separation, reactive cleanup and, finally, high-performance gel permeation chromatography. Egg gram-equivalent doses (g tissue/g egg normalized for egg % lipid) of the final extract (0.02, 0.10, 0.20, 1.0, 2.0, 4.0, 10.0, 20.0 eggEQ) were injected into newly fertilized rainbow trout eggs using triolein as the vehicle. The extract of the lake trout was embryotoxic to rainbow trout, with an LD 50 of 35 eggEQ, based on total cumulative mortality. Gross physical abnormalities characteristic of dioxin exposure, such as hemorrhaging, yolk-sac edema and craniofacial deformities, were observed and showed significant dose-related increases. Sublethal effects in the rainbow trout, such as delayed time to hatch, mild hemorrhaging and moderate yolk-sac edema, resulted from estimated total PCB exposure as low as 8.8 ng/g, and this may have significant implications on Great Lakes lake trout fry and juvenile mortality.

Marine Environmental Research↗

USGS1990

Platinum-group element abundance and distribution in chromite deposits of the Acoje Block, Zambales Ophiolite Complex, Philippines

Platinum-group elements (PGE) occur in ore-grade concentration in some of the chromite deposits related to the ultramafic section of the Acoje Block of the Zambales Ophiolite Complex. The deposits are of three types: Type 1 - associated with cumulate peridotites at the base of the crust; Type 2 - in dunite pods from the top 1 km of mantle harzburgite; and Type 3 - like Type 2, but in deeper levels of the harzburgite. Most of the deposites have chromite compositions that are high in Cr with Cr/(Cr + Al) (expressed as chromium index, Cr#) > 0.6; high-Al (Cr# < 0.6) chromite deposits are relatively rare, occurring as interspersed orebodies in regions of Types 2 and 3. Sulfide-bearing Type 1 high-Cr deposits are PGE-enriched; the high-Al deposits have lowest Ir and Pd. Among the PGEs, Ir ranges from <20 to 550 ppb, Rh from <100 to 1100 ppb, Rh from 0.7 to 760 ppb, Pt from <1.0 to 5960 ppb and Pd from <0.5 to 8350 ppb. Chondrite-normalized (CN) PGE patterns are diverse, and include those with both negative slope (Ir > Pd, thought to be characteristic of PGE-barren deposits) and positive slope (Ir < Pd, characteristic of PGE-rich deposits). Iridium, Ru and Os commonly occur as micron-size laurite (sulfide) inclusions in unfractured chromite. Laurite and native Os are also found as inclusions in interstitial sulfides. Platinum and Pd occur as alloy inclusions (and possibly as solid solution) in interstitial Ni-Cu sulfides and as tellurobismuthides in serpentine and altered sulfides.

Journal of Geochemical Exploration↗

USGS2018

The San Andreas Fault System--Complexities along a major transform fault system and relation to earthquake hazards

The San Andreas Fault System is a 1300-km-long transform boundary that accommodates motion between the North American and Pacific Plates. New technologies and data reveal rich details about the present configuration of faults, distribution of strain and associated seismic hazard on this complex network of faults. This contribution provides a brief summary of the geologic history of the San Andreas Fault System, followed by an introduction to recent research that has changed understanding of the hazards along the main faults. Organized by region, we highlight a selection of recent research using new geodetic techniques, improved topographic data, advanced geochronologic methods, and high-resolution geophysics. The contribution ends with a review of the historic earthquakes on the San Andreas and San Jacinto Faults, comparing these to past ruptures interpreted from paleoseismic studies.

California↗

USGS2011

Surface complexation modeling for predicting solid phase arsenic concentrations in the sediments of the Mississippi River Valley alluvial aquifer, Arkansas, USA

The potential health impact of As in drinking water supply systems in the Mississippi River Valley alluvial aquifer in the state of Arkansas, USA is significant. In this context it is important to understand the occurrence, distribution and mobilization of As in the Mississippi River Valley alluvial aquifer. Application of surface complexation models (SCMs) to predict the sorption behavior of As and hydrous Fe oxides (HFO) in the laboratory has increased in the last decade. However, the application of SCMs to predict the sorption of As in natural sediments has not often been reported, and such applications are greatly constrained by the lack of site-specific model parameters. Attempts have been made to use SCMs considering a component additivity (CA) approach which accounts for relative abundances of pure phases in natural sediments, followed by the addition of SCM parameters individually for each phase. Although few reliable and internally consistent sorption databases related to HFO exist, the use of SCMs using laboratory-derived sorption databases to predict the mobility of As in natural sediments has increased. This study is an attempt to evaluate the ability of the SCMs using the geochemical code PHREEQC to predict solid phase As in the sediments of the Mississippi River Valley alluvial aquifer in Arkansas. The SCM option of the double-layer model (DLM) was simulated using ferrihydrite and goethite as sorbents quantified from chemical extractions, calculated surface-site densities, published surface properties, and published laboratory-derived sorption constants for the sorbents. The model results are satisfactory for shallow wells (10.6 m below ground surface), where the redox condition is relatively oxic or mildly suboxic. However, for the deep alluvial aquifer (21–36.6 m below ground surface) where the redox condition is suboxic to anoxic, the model results are unsatisfactory.

Arkansas↗

USGS2011

Investigating the complex interface where bedrock transforms to regolith

The interface where bedrock transforms to regolith is not planar but rather has a roughness that varies with the scale of observation. The complexity of this surface is manifested in both element-depth and fragment size-depth distributions and may sometimes be related to the longitudinal profiles of watershed streams. The fractal nature of the bedrock-regolith interface means that the interface has a “thickness” which is >20 m in two ridgetop examples from Pennsylvania and Puerto Rico. Such weathering thicknesses, modeled as a function of one-dimensional fluid flow, are affected by the balance between rates of weathering and erosion. One-dimensional models are consistent with weathering advance rates that vary with equilibrium solubility and porefluid velocities (and not reaction kinetics). However, fluid flow is not strictly downward and one-dimensional. Permeability of regolith changes as particle size and bulk density changes with depth. Thus, both downward and lateral flow occurs especially at reaction fronts where reactions change permeability. The rate of weathering advance is, therefore, affected by the 3-dimensional distribution of reaction zones that affect permeability across the watershed. Quantitative models of such phenomena over a range of spatial and temporal scales are needed.

Applied Geochemistry↗

USGS2008

Geolocation of man-made reservoirs across terrains of varying complexity using GIS

The Reservoir Sedimentation Survey Information System (RESIS) is one of the world's most comprehensive databases of reservoir sedimentation rates, comprising nearly 6000 surveys for 1819 reservoirs across the continental United States. Sediment surveys in the database date from 1904 to 1999, though more than 95% of surveys were entered prior to 1980, making RESIS largely a historical database. The use of this database for large-scale studies has been limited by the lack of precise coordinates for the reservoirs. Many of the reservoirs are relatively small structures and do not appear on current USGS topographic maps. Others have been renamed or have only approximate (i.e. township and range) coordinates. This paper presents a method scripted in ESRI's ARC Macro Language (AML) to locate the reservoirs on digital elevation models using information available in RESIS. The script also delineates the contributing watersheds and compiles several hydrologically important parameters for each reservoir. Evaluation of the method indicates that, for watersheds larger than 5 km2, the correct outlet is identified over 80% of the time. The importance of identifying the watershed outlet correctly depends on the application. Our intent is to collect spatial data for watersheds across the continental United States and describe the land use, soils, and topography for each reservoir's watershed. Because of local landscape similarity in these properties, we show that choosing the incorrect watershed does not necessarily mean that the watershed characteristics will be misrepresented. We present a measure termed terrain complexity and examine its relationship to geolocation success rate and its influence on the similarity of nearby watersheds. ?? 2008 Elsevier Ltd. All rights reserved.

Computers & Geosciences↗

USGS2007

Separation of copper, iron, and zinc from complex aqueous solutions for isotopic measurement

The measurement of Cu, Fe, and Zn isotopes in natural samples may provide valuable information about biogeochemical processes in the environment. However, the widespread application of stable Cu, Fe, and Zn isotope chemistry to natural water systems remains limited by our ability to efficiently separate these trace elements from the greater concentrations of matrix elements. In this study, we present a new method for the isolation of Cu, Fe, and Zn from complex aqueous solutions using a single anion-exchange column with hydrochloric acid media. Using this method we are able to quantitatively separate Cu, Fe, and Zn from each other and from matrix elements in a single column elution. Elution of the elements of interest, as well as all other elements, through the anion-exchange column is a function of the speciation of each element in the various concentrations of HCl. We highlight the column chemistry by comparing our observations with published studies that have investigated the speciation of Cu, Fe, and Zn in chloride solutions. The functionality of the column procedure was tested by measuring Cu, Fe, and Zn isotopes in a variety of stream water samples impacted by acid mine drainage. The accuracy and precision of Zn isotopic measurements was tested by doping Zn-free stream water with the Zn isotopic standard. The reproducibility of the entire column separation process and the overall precision of the isotopic measurements were also evaluated. The isotopic results demonstrate that the Cu, Fe, and Zn column separates from the tested stream waters are of sufficient purity to be analyzed directly using a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS), and that the measurements are fully-reproducible, accurate, and precise. Although limited in scope, these isotopic measurements reveal significant variations in δ 65 Cu (− 1.41 to + 0.30‰), δ 56 Fe (− 0.56 to + 0.34‰), and δ 66 Zn (0.31 to 0.49‰) among samples collected from different abandoned mines within a single watershed. Hence, Cu, Fe, and Zn isotopic measurements may be a powerful tool for fingerprinting specific metal sources and/or examining biogeochemical reactions within fresh water systems.

Chemical Geology↗

USGS2023

High-precision ID-TIMS U-Pb geochronology of perovskite (CaTiO3) from the Ice River Complex, southeastern British Columbia

Uranium‑lead perovskite in situ geochronology has become a cornerstone technique for determining the emplacement timing of alkaline, ultrapotassic, and silica-undersaturated igneous rocks, kimberlites, and carbonatites. Accurate in situ dates are dependent on the availability of matrix matched mineral reference materials which themselves are chemically well characterized and dated accurately to the highest possible precision. When dating perovskite to high precision, such as by isotope dilution thermal ionization mass spectrometry (ID-TIMS), appropriately accounting and correcting for the quantity and isotopic composition of Pb incorporated into the crystal upon crystallization (Pb i ) is a large source of uncertainty and potential inaccuracy. Unfortunately, although ultra-high precision perovskite dates are attainable with modern mass spectrometry techniques, the accuracy of applied Pb i compositions, which can be a considerable percentage of total Pb in a crystal, has not kept pace, resulting in percent level inaccuracy on precisely measured isotopic ratios. In an effort to characterize the age and initial Pb isotopic composition of a readily available, relatively pure perovskite endmember (93–98%) which will be useful as a matrix matched age reference material for in situ U-Pb geochronology, we date crystals isolated from three samples from the Ice River Complex (samples 81IR6, I90.3, and I92.30) by ID-TIMS and evaluate their suitability as known-age reference materials. We directly determine the isotopic composition of Pb i in each sample by ID-TIMS measurement of cogenetic low 238 U/ 204 Pb (μ < 500) phlogopite, apatite, and/or clinopyroxene. Using these initial common Pb isotopic compositions, which are significantly more radiogenic than those predicted by age appropriate Pb evolution models, we obtain ultra-precise weighted-mean 206 Pb/ 238 U perovskite dates of 355.83 ± 0.14, 355.04 ± 0.15, and 357.34 ± 0.12 Ma on the three Ice River samples, respectively. These dates are consistent with the relative emplacement ages previously established for units in the Ice River layered ultramafic series based on field relationships. They also demonstrate the feasibility of attaining accurate perovskite dates in instances when maximum precision is critical by utilizing ID-TIMS analysis of cogenetic low uranium phases for direct measurement of Pb i .

British Columbia↗