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Hugh T. Millard

Publications and source records attributed to Hugh T. Millard.

18 recordsLinked to original sources
USGS1998

Paleopedology plus TL, 10Be, and14C dating as tools in stratigraphic and paleoclimatic investigations, Mississippi River Valley, U.S.A.

Thick ( ??? 35 m) loess deposits are present on ridges and high bluffs in the northern-half of the Lower Mississippi Valley (LMV), U.S.A. Detailed descriptions of the loess sections and pedologic, physiochemical, and mineralogic analyses and TL, 14C, and 10Be age determinations, allow preliminary paleoclimatic reconstructions for the late Quaternary of central North America. No age data are available for the oldest (Fifth) loess. 10Be and TL age data suggest a 250-200 ka age for the Fourth or Crowleys Ridge(?) Loess, and indicate that the Loveland or Third Loess is time equivalent to oxygen isotope stage 6, ??? 190-120 ka. A weakly developed paleosol is present in the basal-half of the Loveland. The Sangamon Geosol is present in the upper 5 m and represents all of oxygen isotope stage 5, ??? 130-60 ka. It formed in a climate as warm as, but drier and (or) with greater variation in precipitation, than the present. The Roxana Silt (second loess) was deposited during oxygen isotope stages 4 and 3, ??? 65-26 ka. The early Wisconsinan interglacial-glacial transition, represented by the Sangamon Geosol and the unnamed paleosol in the basal Roxana Silt, was slow. The paleoclimate during the 35 k yr of Roxana deposition was cool to cold and wet. Age and pedologic data indicate that deposition of the Peoria Loess (the youngest) began around 25 ka when the area's climate changed abruptly from cool or cold and wet to cold and dry, with periods of sustained high winds.

Quaternary International↗
USGS1987

Neutron activation determination of iridium, gold, platinum, and silver in geologic samples

Low-level methods for the determination of iridium and other noble metals have become increasingly important in recent years due to interest in locating abundance anomalies associated with the Cretaceous and Tertiary (K-T) boundary. Typical iridium anomalies are in the range of 1 to 100 ??g/kg (ppb). Thus methods with detection limits near 0.1 ??g/kg should be adequate to detect K-T boundary anomalies. Radiochemical neutron activation analysis methods continue to be required although instrumental neutron activation analysis techniques employing elaborate gamma-counters are under development. In the procedure developed in this study samples irradiated in the epithermal neutron facility of the U. S. Geological Survey TRIGA Reactor (Denver, Colorado) are treated with a mini-fire assay technique. The iridium, gold, and silver are collected in a 1-gram metallic lead button. Primary contaminants at this stage are arsenic and antimony. These can be removed by heating the button with a mixture of sodium perioxide and sodium hydroxide. The resulting 0.2-gram lead bead is counted in a Compton suppression spectrometer. Carrier yields are determined by reirradiation of the lead beads. This procedure has been applied to the U.S.G.S. Standard Rock PCC-1 and samples from K-T boundary sites in the Western Interior of North America. ?? 1987 Akade??miai Kiado??.

Journal of Radioanalytical and Nuclear Chemistry A↗
USGS1987

Dinosaurs, spherules, and the “magic” layer: A new K-T boundary clay site in Wyoming

A new Cretaceous-Tertiary (K-T) boundary clay site has been found along Dogie Creek in Wyoming in the drainage of Lance Creek—the type area of the Lance Formation of latest Cretaceous age. The boundary clay was discovered in the uppermost part of the Lance Formation, 4–7 cm beneath the lowest lignite in the Paleocene Fort Union Formation and approximately 1 m above a fragmented dinosaur bone. The boundary clay consists of a basal kaolinitic claystone layer as much as 3 cm thick containing hollow goyazite spherules, overlain by a 2–3 mm smectitic layer (the “magic” layer) containing both shock-metamorphosed minerals and an iridium anomaly of 21 ppb. A palynological break coincides with the base of the claystone layer; numerous Late Cretaceous palynomorph species terminate at this boundary. The paleontological significance of this new boundary site lies in its close association with the well-studied assemblage of dinosaurs and other vertebrates and flora within the type area of the Lance Formation. The spherules at the Dogie Creek site are extremely well preserved by virtue of their replacement by the mineral goyazite. This preservation should facilitate the resolution of the origin of the spherules and of their host layer.

Wyoming↗
USGS1984

Geochemical investigation of Archaean Bimodal and Dwalile metamorphic suites, Ancient Gneiss Complex, Swaziland

The bimodal suite (BMS) comprises leucotonalitic and trondhjemitic gneisses interlayered with amphibolites. Based on geochemical parameters three main groups of siliceous gneiss are recognized: (i) SiO 2 < 73%, Al 2 O 3 > 14%, and fractionated light rare-earth element (REE) and flat heavy REE patterns; (ii) SiO 2 and Al 2 O 3 contents similar to (i) but with strongly fractionated REE patterns with steep heavy REE slopes; (iii) SiO 2 > 73%, Al 2 O 3 < 14%, Zr ∼ 500 ppm and high contents of total REE having fractionated light REE and flat heavy REE patterns with large negative Eu anomalies. The interlayered amphibolites have major element abundances similar to those of basaltic komatiites, Mg-tholeiites and Fe-rich tholeiites. The former have gently sloping REE patterns, whereas the Mg-tholeiites have non-uniform REE patterns ranging from flat (∼ 10 times chondrite) to strongly light REE-enriched. The Fe-rich amphibolites have flat REE patterns at 20–30 times chondrite. The Dwalile metamorphic suite, which is preserved in the keels of synforms within the BMS, includes peridotitic komatiites that have depleted light REE patterns similar to those of compositionally similar volcanics in the Onverwacht Group, Barberton, basaltic komatiites and tholeiites. The basaltic komatiites have REE patterns parallel to those of the BMS basaltic komatiites but with lower total REE contents. The Dwalile tholeiites have flat REE patterns. The basic and ultrabasic liquids were derived by partial melting of a mantle source which may have been heterogeneous or the heterogeneity may have resulted from sequential melting of the mantle source. The Fe-rich amphibolites were derived either from liquids generated at shallow levels or from liquids generated at depth which subsequently underwent extensive fractionation.

Mankayane district↗
USGS1981

The distribution of uranium and thorium in granitic rocks of the basin and range province, Western United States

Some secondary uranium deposits are thought to have formed from uranium derived by the weathering of silicic igneous rocks such as granites, rhyolites, and tuffs. A regional geochemical survey was made to determine the distribution of uranium and thorium in granitic rocks of the Basin and Range province in order to evaluate the potential for secondary uranium occurrences in the area. The resulting geochemical maps of uranium, thorium, and the Th:U ratio may be useful in locating target areas for uranium exploration. The granites were sampled according to a five-level, nested, analysis-of-variance design, permitting estimates to be made of the variance due to differences between:(1) two-degree cells; (2) one-degree cells; (3) plutons; (4) samples; and (5) analyses. The cells are areas described in units of degrees of latitude and longitude. The results show that individual plutons tend to differ in uranium and thorium concentrations, but that each pluton tends to be relatively homogeneous. Only small amounts of variance occur at the two degree and the between-analyses levels. The three geochemical maps that were prepared are based on one-degree cell means. The reproducibility of the maps is U > Th ⪢ Th:U. These geochemical maps may be used in three methods of locating target areas for uranium exploration. The first method uses the concept that plutons containing the greatest amounts of uranium may supply the greatest amounts of uranium for the formation of secondary uranium occurrences. The second method is to examine areas with high thorium contents, because thorium and uranium are initially highly correlated but much uranium could be lost by weathering. The third method is to locate areas in which the plutons have particularly high Th:U ratios. Because uranium, but not thorium, is leached by chemical weathering, high Th:U ratios suggest a possible loss of uranium and possibly a greater potential for secondary uranium occurrences to be found in the area.

Arizona, California, Nevada, Utah↗
USGS1980

Deep-sea spherules from Pacific clay: Mass distribution and influx rate

From 411 kg of Pacific clay, 22 mg of stony spherules and 50 mg of iron spherules larger than 150 μm were concentrated. The extraterrestrial origin of these particles was evaluated with the aid of both optical and electron microscopy as well as atomic absorption elemental analysis. The integral number ( N ) of stony particles from this sediment in the mass (M) range 20–300 μg is given by N ( > M ( g )) = 5.13 × 10 −6 × M −1.65 . The world-wide influx rate of stony particles in the mass range which survive atmospheric heating and ocean sediment storage is calculated to be 90 tons/yr. The relative contributions of ablation debris vs fused interplanetary dust to the influx of stony spherules is discussed, but as yet the question remains unanswered.

Geochimica et Cosmochimica Acta↗
USGS1978

The geochemical nature of the Archean Ancient Gneiss Complex and Granodiorite Suite, Swaziland: A preliminary study

The Ancient Gneiss Complex (AGC) of Swaziland, an Archean gray gneiss complex, lies southeast and south of the Barberton greenstone belt and includes the most structurally complex and highly metamorphosed portions of the eastern Kaapvaal craton. The AGC is not precisely dated but apparently is older than 3.4 Ga. The AGC consists of three major units: (a) a bimodal suite of closely interlayered siliceous, low-K gneisses and metabasalt; (b) homogeneous tonalite gneiss; and (c) interlayered siliceous microcline gneiss, metabasalt, and minor metasedimentary rocks - termed the metamorphite suite. A geologically younger gabbro-diorite-tonalite-trondhjemite suite, the Granodiorite Suite, is spatially associated with the AGC and intrusive into it. The bimodal suite consists largely of two types of low-K siliceous gneiss: one has SiO 2 < 75%, Al 2 O 3 > 14%, low Rb/Sr ratios, and depleted heavy rare earth elements (REE's); the other has SiO 2 > 75%, Al 2 O 3 < 13%, high Rb/Sr ratios, and relatively abundant REE's except for negative Eu anomalies. The interlayered metabasalt ranges from komatiitic to tholeiitic compositions. Lenses of quartz monzonitic gneiss of K 2 O/Na 2 O close to 1 form a minor part of the bimodal suite. Tonalitic to trondhjemitic migmatite locally is abundant and has major-element abundances similar to those of non-migmatitic varieties. The siliceous gneisses of the metamorphic suite show low Al 2 O, K 2 O/Na 2 O ratios of about 1, high Rb/Sr ratios, moderate REE abundances and negative Eu anomalies. K/Rb ratios of siliceous gneisses of the bimodal suite are very low (∼130); of the tonalitic gneiss, low (∼225); of the siliceous gneiss of the metamorphite suite, moderate (∼300); and of the Granodiorite Suite, high (∼400). Rocks of the AGC differ geochemically in several ways from the siliceous volcanic and hypabyssal rocks of the Upper Onverwacht Group and from the diapirs of tonalite and trondhjemite that intrude the Swaziland Group.

Precambrian Research↗
USGS1977

A comparison of some analytical techniques for determining uranium, thorium, and potassium in granitic rocks

Geochemical exploration for uranium requires accurate and precise determinations of low-level concentrations. We have used seven different techniques and four different treatments of the fluorometric method to analyze for uranium in granitic rocks. In addition we have used four analytical techniques for thorium and three analytical techniques for potassium, two elements that are commonly present in anomalous amounts within uranium provinces. Our results show that commonly used techniques for thorium and potassium determinations are both adequately precise and accurate, but that many techniques used for uranium determinations lack the necessary precision or accuracy for complete geochemical prospecting. We suggest that a combination of delayed-neutron determinations for uranium and γ -ray spectrometric analyses for radium equivalent uranium, thorium, and potassium provides the best data base for geochemical exploration for uranium. If more detailed interpretations are desired, the combination of γ -ray spectrometry and α -spectrometry may be best. Carefully done fluorometric analyses should be adequate for water, ore, mineralized rock, and other applications where high precision and accuracy are not required.

Journal of Research of the U.S. Geological Survey↗
USGS1972

A neutron activation analysis procedure for the determination of uranium, thorium and potassium in geologic samples

A neutron activation analysis procedure was developed for the determination of uranium, thorium and potassium in basic and ultrabasic rocks. The three elements are determined in the same 0.5-g sample following a 30-min irradiation in a thermal neutron flux of 2·10 12 n·cm −2 ·sec −1 . Following radiochemical separation, the nuclides 239 U (T=23.5 m), 233 Th (T=22.2 m) and 42 K (T=12.36 h) are measured by β-counting. A computer program is used to resolve the decay curves which are complex owing to contamination and the growth of daughter activities. The method was used to determine uranium, throium and potassium in the U. S. Geological Survey standard rocks DTS-1, PCC-1 and BCR-1. For 0.5-g samples the limits of detection for uranium, throium and potassium are 0.7, 1.0 and 10 ppb, respectively.

Journal of Radioanalytical Chemistry↗
USGS1969

Establishment of gold-quartz standard GQS-1

A homogeneous gold-quartz standard, GQS-1, was prepared from a heterogeneous gold-bearing quartz by chemical treatment. The concentration of gold in GQS-1 was determined by both instrumental neutron activation analysis and radioisotope dilution analysis to be 2.61?0.10 parts per million. Analysis of 10 samples of the standard by both instrumental neutron activation analysis and radioisotope dilution analysis failed to reveal heterogeneity within the standard. The precision of the analytical methods, expressed as standard error, was approximately 0.1 part per million. The analytical data were also used to estimate the average size of gold particles. The chemical treatment apparently reduced the average diameter of the gold particles by at least an order of magnitude and increased the concentration of gold grains by a factor of at least 4,000.

Circular↗