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Joseph E. Taggart

Publications and source records attributed to Joseph E. Taggart.

9 recordsLinked to original sources
USGS2024

Reassessment of the volkonskoite-chromian smectite nomenclature problem.

The name volkonskoite was first used in 1830 to describe a bright blue-green, chromium-bearing clay material from the Okhansk region, west of the Ural Mountains, U.S.S.R. Since that time, the name has been applied to numerous members of the smectite group of clay minerals, although the reported chromium content has ranged from 1% to about 30% Cr 2 O 3 . The name has also been applied to some chromian chlorites. Because volkonskoite has been used for materials that differ not only in their chromium content but also in their basic structure, the species status of the mineral has been unclear. To resolve this uncertainty, two specimens of volkonskoite from (1) Mount Efimiatsk, the type locality in the Soviet Union (USNM 16308) and (2) the Okhansk region in the Perm Basin, U.S.S.R. (USNM R4820), were examined by several mineralogical techniques. Neotype sample 16308 has the following structural formula: (Ca 0.11 Mg 0.11 Fe 2+ 0.03 K 0.02 )(Cr 1.18 Mg 0.78 Fe 3+ 0.29 Ca 0.02 )(Si 3.50 Al 0.51 )O 10 (OH) 2 ⋅3.64H 2 O. Sample R4820 has the following structural formula: (Ca 0.25 Mg 0.05 Fe 2+ 0.01 K 0.03 Mn 0.01 )(Cr 1.07 Mg 0.75 Fe 3+ 0.35 (Si 3.59 Al 0.43 )O 10 (OH) 2 ⋅4.22H 2 O. Mössbauer spectroscopy indicates that 91% and 98% of the iron is present as Fe 3+ in samples 16308 and R4820, respectively. X-ray powder diffraction patterns of both samples have broad lines corresponding to minerals of the smectite group. On the basis of these data, volkonskoite appears to be a dioctahedral member of the smectite group that contains chromium as the dominant cation in the octahedral layer. Smectites containing less than this amount of octahedral chromium should not be called volkonskoite, but should be named by chemical element adjectives, e.g., chromian montmorillonite, chromian nontronite.

Clays and Clay Minerals↗
USGS2010

Whole-rock analyses of core samples from the 1988 drilling of Kilauea Iki lava lake, Hawaii

This report presents and evaluates 64 major-element analyses of previously unanalyzed Kilauea Iki drill core, plus three samples from the 1959 and 1960 eruptions of Kilauea, obtained by X-ray fluorescence (XRF) analysis during the period 1992 to 1995. All earlier major-element analyses of Kilauea Iki core, obtained by classical (gravimetric) analysis, were reported and evaluated in Helz and others (1994). In order to assess how well the newer data compare with this earlier suite of analyses, a subset of 24 samples, which had been analyzed by classical analysis, was reanalyzed using the XRF technique; those results are presented and evaluated in this report also. The XRF analyses have not been published previously. This report also provides an overview of how the chemical variations observed in these new data fit in with the chemical zonation patterns and petrologic processes inferred in earlier studies of Kilauea Iki.

Kilauea Iki Lava Lake↗
USGS2009

Inorganic chemical composition and chemical reactivity of settled dust generated by the World Trade Center building collapse

Samples of dust deposited around lower Manhattan by the September 11, 2001, World Trade Center (WTC) collapse have inorganic chemical compositions that result in part from the variable chemical contributions of concrete, gypsum wallboard, glass fibers, window glass, and other materials contained in the buildings. The dust deposits were also modified chemically by variable interactions with rain water or water used in street washing and fire fighting. Chemical leach tests using deionized water as the extraction fluid show the dust samples can be quite alkaline, due primarily to reactions with calcium hydroxide in concrete particles. Calcium and sulfate are the most soluble components in the dust, but many other elements are also readily leached, including metals such as Al, Sb, Mo Cr, Cu, and Zn. Indoor dust samples produce leachates with higher pH, alkalinity, and dissolved solids than outdoor dust samples, suggesting most outdoor dust had reacted with water and atmospheric carbon dioxide prior to sample collection. Leach tests using simulated lung fluids as the extracting fluid suggest that the dust might also be quite reactive in fluids lining the respiratory tract, resulting in dissolution of some particles and possible precipitation of new phases such as phosphates, carbonates, and silicates. Results of these chemical characterization studies can be used by health scientists as they continue to track and interpret health effects resulting from the short-term exposure to the initial dust cloud and the longer-term exposure to dusts resuspended during cleanup.

New York↗
USGS2008

Catalog of Mount St. Helens 2004-2007 dome samples with major- and trace-element chemistry

Sampling and analysis of eruptive products at Mount St. Helens is an integral part of volcano monitoring efforts conducted by the U.S. Geological Survey?s Cascades Volcano Observatory (CVO). The objective of our eruption sampling program is to enable petrological assessments of pre-eruptive magmatic conditions, critical for ascertaining mechanisms for eruption triggering and forecasting potential changes in eruption behavior. This report provides a catalog of near-vent lithic debris and new dome-lava collected during 34 intra-crater sampling forays throughout the October 2004 to October 2007 (2004-7) eruptive interval at Mount St. Helens. In addition, we present comprehensive bulk-rock geochemistry for a time-series of representative (2004-7) eruption products. This data, along with that in a companion report on Mount St. Helens 2004 to 2006 tephra by Rowe and others (2008), are presented in support of the contents of the U.S. Geological Survey Professional Paper 1750 (Sherrod and others, eds., 2008). Readers are referred to appropriate chapters in USGS Professional Paper 1750 for detailed narratives of eruptive activity during this time period and for interpretations of sample characteristics and geochemical data. The suite of rock samples related to the 2004-7 eruption of Mount St. Helens and presented in this catalog are archived at the David A. Johnson Cascades Volcano Observatory, Vancouver, Wash. The Mount St. Helens 2004-7 Dome Sample Catalogue with major- and trace-element geochemistry is tabulated in 3 worksheets of the accompanying Microsoft Excel file, of2008-1130.xls. Table 1 provides location and sampling information. Table 2 presents sample descriptions. In table 3, bulk-rock major and trace-element geochemistry is listed for 44 eruption-related samples with intra-laboratory replicate analyses of 19 dacite lava samples. A brief overview of the collection methods and lithology of dome samples is given below as an aid to deciphering the dome sample catalog. This is followed by an explanation of the categories of sample information (column headers) in Tables 1 and 2. A summary of the analytical methods used to obtain the geochemical data in this report introduces the presentation of major- and trace-element geochemistry of 2004-7 Mount St. Helens dome samples in table 3. Intra-laboratory results for the USGS AGV-2 standard are presented (tables 4 and 5), which demonstrate the compatibility of chemical data from different sources.

Open-File Report↗
USGS2003

Correlation, sedimentology, structural setting, chemical composition, and provenance of selected formations in Mesoproterozoic Lemhi Group, central Idaho

A unit of the Mesoproterozoic Apple Creek Formation of the Lemhi Range previously was correlated with part of the lower subunit of the Mesoproterozoic Yellowjacket Formation in the Salmon River Mountains. Strata currently assigned to the middle subunit of the Yellowjacket Formation lie conformably above the Apple Creek unit in the Salmon River Mountains, and are here renamed the banded siltite unit and reassigned to the Apple Creek Formation. Almost all of the banded siltite unit is preserved within the Salmon River Mountains, where it grades upward into clastic rocks that currently are assigned to the upper subunit of the Yellowjacket Formation and that here are reassigned to the Gunsight Formation. The banded siltite unit of the Apple Creek Formation is composed of a turbidite sequence, as recognized by previous workers. Uppermost strata of the unit were reworked by currents, possibly storm generated, and adjusted to a high water content by developing abundant soft-sediment deformation features. Basal strata of the overlying Gunsight Formation in the Salmon River Mountains display abundant hummocky crossbeds, storm-generated features deposited below fair-weather wave base, that are conformable above the storm-reworked deposits. The hummocky crossbedded strata grade upward into marine shoreface strata deposited above fair-weather wave base, which in turn are succeeded by fluvial strata. Hummocky and shoreface strata are absent from the Gunsight Formation in the Lemhi Range. The major thickness of the Gunsight Formation in both the Salmon River Mountains and the Lemhi Range is composed of fluvial rocks, transitional in the upper part into marine rocks of the Swauger Formation. The fluvial strata are mainly characterized by stacked sheets of metasandstone and coarse siltite; they are interpreted as deposits of braided rivers. The Poison Creek thrust fault of the Lemhi Range extends northwestward through the study area in the east-central part of the Salmon River Mountains. The Apple Creek and Gunsight Formations on the southwest side of the thrust fault were transported to the northeast as part of the Poison Creek thrust sheet. A segment of the thrust fault within the Gunsight Formation in the Salmon River Mountains subsequently underwent normal displacement. Along this segment, lower Gunsight strata on the southwest were juxtaposed against upper Gunsight and Swauger strata on the northeast.

Professional Paper↗
USGS2002

Statistical tables and charts showing geochemical variation in the Mesoproterozoic Big Creek, Apple Creek, and Gunsight formations, Lemhi group, Salmon River Mountains and Lemhi Range, central Idaho

The principal purpose of this report is to provide a reference archive for results of a statistical analysis of geochemical data for metasedimentary rocks of Mesoproterozoic age of the Salmon River Mountains and Lemhi Range, central Idaho. Descriptions of geochemical data sets, statistical methods, rationale for interpretations, and references to the literature are provided. Three methods of analysis are used: R-mode factor analysis of major oxide and trace element data for identifying petrochemical processes, analysis of variance for effects of rock type and stratigraphic position on chemical composition, and major-oxide ratio plots for comparison with the chemical composition of common clastic sedimentary rocks.

Idaho↗
USGS1987

Inter-laboratory comparison of X-ray fluorescence analyses of eruptive products of El Chichón Volcano, Chiapas, Mexico

An inter-laboratory comparison has been made of X-ray fluorescence analyses of 10 samples of lava and pumices from El Chichón Volcano, Chiapas, Mexico. Some determinations of major-element constituents agree within analytical uncertainty, whereas others exchibit significant bias. Analyses carried out at the Michigan Technological University (MTU) laboratory are systematically lower in MgO (26–48%), Fe total (5–18%), CaO (4–15%) and higher in K 2 O (0–15%) than analyses made at the U.S. Geological Survey (USGS) Denver laboratory. These differences are ascribed in part to a complex combination of calibration assumptionsand mineralogical and particle-size effects inherent in the use of pressed rock-powder pellets in the analytical procedure of the MTU laboratory. Other, but as yet unknown, differences in sample preparation and/or analytical technique may also be important; effects related to natural sample inhomogeneityare believed to be insignificant. The inter-laboratory differences in the analytical data complicated accurate assessment of whether El Chichón magmas have changed composition during the past 300 000 a. Knowledge of such change is needed for understanding petrogenetic history and for such related studies as evaluation of volcanic hazards.

Applied Geochemistry↗
USGS1986

Zimbabweite, a new alkali-lead arsenic tantalate from St Anns mine, Karoi district, Zimbabwe

Zimbabweite (Na,K) 2 PbAs 4 (Ta,Nb,Ti) 4 O 18 , a new mineral with trivalent arsenic, has been recognized at St Anns mine, southeast of Miami, Karoi district, Zimbabwe, in kaolinized pegmatite and dump material. The mineral is honey yellow-brown in large crystals, which are as much as 1 x 1 x 2 cm, and is clear pale yellow in thin fragments. Oxidation results in darkening of the color. There is one excellent cleavage, {010}. Zimbabweite has a Mohs hardness of 5 to 5.5, a white streak, adamantine luster, brittle fracture, is not magnetic, and does not fluoresce under either short wave or long wave ultraviolet light. d m = 6.20(3) and d c = 6.16 g/cm3. Optically, the mineral is biaxial (+), 2V Z = about 80°. Mean reflectances in air for an {010} = X-Z cleavage plate are : 589 nm--16.6 %, 470 nm--17.7 %, 546 nm--17.1 %, 650 nm--16.4 %. The indices of refraction determined by immersion methods are all greater than 2.10. Optic axis dispersion is very strong with ν > r, a = Z, b = Y, and c = X. The mineral is very pale yelow and is moderately pleochroic and X = pale yellow brown, Y = light reddish brown, and Z =reddish brown. Zimbabweite is insoluble in common acids or bases. A chemical analysis yielded, in weight percent, Ta 2 O 5 46.5, As 2 O 3 26.5, PbO 15.0, Nb 2 O 5 4.8, Na 2 O 3.1, K 2 O 1.5, TiO 2 1.4, BaO 0.4, UO 2 0.3, Bi 2 O 3 0.2, H 2 O (total) 0.19, SnO 2 0.1, F 0.04, SrO 0.02, total 100.05. A calculated formula is : (Na 1.51 K 0.48 Ba 0.04 ) Σ2.03 Pb 1.01 (As 4.03 Bi 0.01 ) Σ4.04 (Ta 3.17 Nb 0.55 Ti 0.26 U 0.02 Sn 0.01 ) Σ4.01 O 18 . Zimbabweite is orthorhombic, space group is Ccma or Cc2a , with a = 12.233(2)Å, b = 15.292(2)Å, c = 8.665(2)Å, V = 1621. 0(4) Å 3 , with Z = 4. No structural relationship between zimbabweite and any other tantalate minerals is apparent.

Karoi District↗