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At least 91 records · Page 5Linked to original sources
USGS2006

Coseismic and initial postseismic deformation from the 2004 Parkfield, California, earthquake, observed by global positioning system, electronic distance meter, creepmeters, and borehole strainmeters

Global Positioning System (GPS), electronic distance meter, creepmeter, and strainmeter measurements spanning the M 6.0 Parkfield, California, earthquake are examined. Using these data from 100 sec through 9 months following the main-shock, the Omori's law, with rate inversely related to time, l/t p and p ranging between 0.7 and 1.3, characterizes the time-dependent deformation during the post-seismic period; these results are consistent with creep models for elastic solids. With an accurate function of postseismic response, the coseismic displacements can be estimated from the high-rate, 1-min sampling GPS; and the coseismic displacements are approximately 75% of those estimated from the daily solutions. Consequently, fault-slip models using daily solutions overestimate coseismic slip. In addition, at 2 months and at 8 months following the mainshock, postseismic displacements are modeled as slip on the San Andreas fault with a lower bound on the moment exceeding that of the coseismic moment.

Bulletin of the Seismological Society of America↗
USGS2011

Visualizing trace element distribution in quartz using cathodoluminescence, electron microprobe, and laser ablation-inductively coupled plasma-mass spectrometry

Cathodoluminescent (CL) textures in quartz reveal successive histories of the physical and chemical fluctuations that accompany crystal growth. Such CL textures reflect trace element concentration variations that can be mapped by electron microprobe or laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). Trace element maps in hydrothermal quartz from four different ore deposit types (Carlin-type Au, epithermal Ag, porphyry-Cu, and MVT Pb-Zn) reveal correlations among trace elements and between trace element concentrations and CL textures. The distributions of trace elements reflect variations in the physical and chemical conditions of quartz precipitation. These maps show that Al is the most abundant trace element in hydrothermal quartz. In crystals grown at temperatures below 300 °C, Al concentrations may vary by up to two orders of magnitude between adjacent growth zones, with no evidence for diffusion. The monovalent cations Li, Na, and K, where detectable, always correlate with Al, with Li being the most abundant of the three. In most samples, Al is more abundant than the combined total of the monovalent cations; however, in the MVT sample, molar Al/Li ratios are ~0.8. Antimony is present in concentrations up to ~120 ppm in epithermal quartz (~200–300 °C), but is not detectable in MVT, Carlin, or porphyry-Cu quartz. Concentrations of Sb do not correlate consistently with those of other trace elements or with CL textures. Titanium is only abundant enough to be mapped in quartz from porphyry-type ore deposits that precipitate at temperatures above ~400 °C. In such quartz, Ti concentration correlates positively with CL intensity, suggesting a causative relationship. In contrast, in quartz from other deposit types, there is no consistent correlation between concentrations of any trace element and CL intensity fluctuations.

American Mineralogist↗
USGS1976

Electronic thermal sensor and Data Collection Platform technology: Part 5 in Thermal surveillance of active volcanoes using the Landsat-1 Data Collection System

Five Data Collection Platforms (DCP) were integrated electronically with thermall sensing systems, emplaced and operated in an analog mode at selected thermally significant volcanic and geothermal sites. The DCP's transmitted 3260 messages comprising 26,080 ambient, surface, and near-surface temperature records at an accuracy of ±1.15 °C for 1121 instrument days between November 14, 1972 and April 17, 1974. In harsh, windy, high-altitude volcanic environments the DCP functioned best with a small dipole antenna. Sixteen kg of alkaline batteries provided a viable power supply for the DCP systems, operated at a low-duty cycle, for 5 to 8 months. A proposed solar power supply system would lengthen the period of unattended operation of the system considerably. Special methods of data handling such as data storage via a proposed memory system would increase the significance of the twice-daily data reception enabling the DCP's to record full diurnal-temperature cycles at volcanic or geothermal sites. Refinements in the temperature-monitoring system designed and operated in experiment SR 251 included a backup system consisting of a multipoint temperature scanner, a servo mechanism and an analog-to-digital recorder. Improvements were made in temperature-probe design and in construction of corrosion-resistant seals by use of a hydrofluoric-acid-etching technique.

Final Report↗
USGS2017

Continued geophysical logging near the GMH Electronics National Priorities List Superfund site near Roxboro, North Carolina

The U.S. Geological Survey South Atlantic Water Science Center collected borehole geophysical logs and images and continuous water-level data near the GMH Electronics National Priorities List Superfund site near Roxboro, North Carolina, during December 2012 through July 2015. Previous work by the U.S. Geological Survey South Atlantic Water Science Center at the site involved the collection of borehole geophysical log data in 15 wells, in addition to surface geologic mapping and passive diffusion bag sampling. In a continued effort to assist the U.S. Environmental Protection Agency in developing a conceptual groundwater model to assess current contaminant distribution and future migration of contaminants, more than 900 subsurface features (primarily fracture orientations) in 10 open borehole wells were delineated and continuous water-level data information from 14 monitoring wells within close proximity of the initially drilled boreholes was collected to observe any induced water-level fluctuations during drilling operations

North Carolina↗
USGS2013

Geophysical logging and geologic mapping data in the vicinity of the GMH Electronics Superfund site near Roxboro, North Carolina

Geologic mapping, the collection of borehole geophysical logs and images, and passive diffusion bag sampling were conducted by the U.S. Geological Survey North Carolina Water Science Center in the vicinity of the GMH Electronics Superfund site near Roxboro, North Carolina, during March through October 2011. The study purpose was to assist the U.S. Environmental Protection Agency in the development of a conceptual groundwater model for the assessment of current contaminant distribution and future migration of contaminants. Data compilation efforts included geologic mapping of more than 250 features, including rock type and secondary joints, delineation of more than 1,300 subsurface features (primarily fracture orientations) in 15 open borehole wells, and the collection of passive diffusion-bag samples from 42 fracture zones at various depths in the 15 wells.

North Carolina↗
USGS2003

Making USGS information effective in the electronic age

Executive Summary -- The USGS Coastal and Marine Geology Program (CMGP) held a workshop on 'Making USGS Information Effective in the Electronic Age' in Woods Hole, MA, on 6-8 February 2001. The workshop was designed to address broad issues of knowledge and communication, and to help develop the mission, vision, and goals of the National Knowledge Bank called for in the 1999 NRC review of the CMGP. Presentations led by historians and philosophers yield to a wide-ranging review and discussion of the role of USGS science in society: USGS science is important to government to understand certain complicated public policy issues (such as the environment), but we must participate in two-way public dialogs to increase our relevance and usefulness. Presentations led by USGS communications experts reviewed the principles of audience analysis and effective communications: this focused look at audiences, markets, and products provided an introduction to the behaviors, the tools, and the terminology that might be applied to public discourse. Presentations by several information technology experts showed the potential - and pitfalls - of current schemes for Web-based information access. Finally, several brainstorming sessions developed action items, vision, and characteristics of a knowledge bank. Based on the workshop discussions and results, the authors developed the National Knowledge Bank Mission, Vision, and Goals statements.

Open-File Report↗
USGS2010

Examination of Libby, Montana, Fill Material for Background Levels of Amphibole from the Rainy Creek Complex Using Scanning Electron Microscopy and X-Ray Microanalysis

Natural background levels of Libby-type amphibole in the sediment of the Libby valley in Montana have not, up to this point, been determined. The purpose of this report is to provide the preliminary findings of a study designed by both the U.S. Geological Survey and the U.S. Environmental Protection Agency and performed by the U.S. Geological Survey. The study worked to constrain the natural background levels of fibrous amphiboles potentially derived from the nearby Rainy Creek Complex. The material selected for this study was sampled from three localities, two of which are active open-pit sand and gravel mines. Seventy samples were collected in total and examined using a scanning electron microscope equipped with an energy dispersive x-ray spectrometer. All samples contained varying amounts of feldspars, ilmenite, magnetite, quartz, clay minerals, pyroxene minerals, and non-fibrous amphiboles such as tremolite, actinolite, and magnesiohornblende. Of the 70 samples collected, only three had detectable levels of fibrous amphiboles compatible with those found in the rainy creek complex. The maximum concentration, identified here, of the amphiboles potentially from the Rainy Creek Complex is 0.083 percent by weight.

Open-File Report↗
USGS2022

Results of automated scanning electron microscope (SEM) analyses of rock and stream sediment samples from the Taurus porphyry copper deposit area, Tanacross quadrangle, eastern Alaska

Numerous porphyry copper-molybdenum-gold and epithermal deposits define a belt that extends from Eastern Alaska to western Yukon, Canada. An orientation study conducted near the Taurus porphyry deposit was designed to test methods that require minimal sample collection, preparation, and analytical time to determine the viability of indicator mineral studies as a reconnaissance exploration method. Bulk stream sediments and altered and mineralized rocks were sieved to the 0.105−0.25 millimeter fraction (+140, −60 mesh) and passed over a shaking table to create a moderate to heavy mineral separate that was mounted in epoxy and subsequently analyzed using automated scanning electron microscope (SEM) techniques. Seven polished thin sections of core were also analyzed. Among the advantages of automated SEM techniques compared to visual mineral identification are that thousands of grains can be rapidly identified in each sample (about 1 hour per sample) and small quantities of indicator minerals that may be missed during traditional visual analyses can be detected. Automated SEM analyses of stream sediment and rock samples show that specific minerals (chalcopyrite, bornite, and jarosite) are indicators of potential mineralized areas. Svanbergite, an aluminum sulfate phosphate mineral, was identified in mineralized rocks and in nearly all stream sediment samples (up to 9 kilometers) downstream from the Taurus and other porphyry occurrences but not epithermal occurrences. It was not identified in areas with no known mineralization and thus it is possibly one of the best indicator minerals for porphyry copper (+/- molybdenum, gold) occurrences.

Alaska↗
USGS1995

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of organochlorine pesticides and polychlorinated biphenyls in bottom sediment by dual capillary-column gas chromatography with electron-capture detection

A method for the determination of 30 individual organochlorine pesticides, total toxaphene, and total polychlorinated biphenyls (PCBs) in bottom sediment is described. The method isolates the pesticides and PCBs by solvent extraction with dichlorobenzene, removes inorganic sulfur, large naturally occurring molecules, and other unwanted interferences by gel permeation chromatography, and further cleans up and class fractionates the extract using adsorption chromatography. The com- pounds then are instrumentally determined using dual capillary-column gas chromatography with electron-capture detection. Reporting limits range from 1 to 5 micrograms per kilogram for 30 individual pesticides, 50 micrograms per kilogram for total PCBs, and 200 micrograms per kilogram for total toxaphene. The method also is designed to allow the simultaneous isolation of 79 other semivolatile organic compounds from the sediment, which are separately quantified using gas chromatography with mass spectrometric detection. The method was developed in support of the U.S. Geological Survey's National Water-Quality Assessment program.

Open-File Report↗
USGS2023

Scanning electron microscope images of sand and silt from the early MIS4–MIS3 Roxana Silt, Phillips Bayou, Arkansas

The age and source of the late Pleistocene Roxana Silt in the Mississippi Valley have been studied since the middle 1800s. Published age and paleoenvironmental data for the Roxana Silt in the Mississippi Valley show that deposition occurred from late marine isotope stage 5 (MIS5) through late marine isotope stage 3 (MIS3) (80–30 kilo-annum [ka]), when the warm to hot interglacial climate of early to middle MIS5 (about 130 to about 80 ka) was transitioning to a considerably cooler and wetter climate. Scanning electron microscopy/energy dispersive X-ray (SEM/EDS) analysis of silt and sand grains from the Roxana Silt exposed in an abandoned borrow pit near Phillips Bayou, Arkansas, was performed as part of a 1990s study of late middle and late Pleistocene loess in the unglaciated lower Mississippi Valley. Results from that study were summarized in 1990s publications, but the data for sand and silt grain morphology and mineralogy were not published. Some of the SEM/EDS analyses of the Roxana Silt from that late 1990s study are presented in this report. Combined with previously published chronostratigraphic and pedostratigraphic data for the Roxana Silt at Phillips Bayou, the SEM/EDS data indicate some degree of syndepositional weathering and pedogenic alteration during and after gradual eolian deposition in late marine isotope stage 4 (MIS4) and MIS3 (about 60 to about 30 ka). Results from the SEM/EDS analyses support previously published paleoclimate interpretations indicating that at least as far south as northern Mississippi, the climate of the Mississippi Valley in MIS4 and MIS3 (about 70 to about 30 ka) was cool to cold and humid to wet.

Arkansas↗
USGS2004

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Determination of organochlorine pesticides and polychlorinated biphenyls in bottom and suspended sediment by gas chromatography with electron-capture detection

A method applicable for the determination of 19 organochlorine (OC) pesticides, including total toxaphene as a complex mixture, and 3 polychlorinated biphenyl (PCB) mixtures as Aroclor equivalents--Aroclor 1016/1242, 1254, and 1260--in soil, aquatic bottom sediment, and suspended sediment is described. Method performance data are presented. The solvent system is designed to extract simultaneously selected OC pesticides and PCBs from the same sample matrix. The compounds are extracted by conventional Soxhlet extraction with dichloromethane, followed by partial isolation using gel permeation chromatography (GPC) to remove inorganic sulfur and large naturally present molecules from the sediment extract. The aliquot of extract collected from the GPC for OCs (OC pesticides and PCBs) is split into two sample fractions by alumina/silica combined-column chromatography, followed by Florisil adsorption chromatography to remove interfering compounds in the second fraction. The OC fractions are analyzed by dual capillary-column gas chromatography with electron-capture detection (GC/ECD). This report is limited to the determination of selected OC pesticides and PCBs by GC/ECD using this method. Interim reporting levels (IRLs) have been set at 0.400 to 3.12 micrograms per kilogram for 18 individual OC pesticides, 200 micrograms per kilogram for toxaphene, and 4.04 to 4.68 micrograms per kilogram for the PCBs, based on a sample size of 25-gram equivalent dry weight. These reporting levels may change following additional determinations of method detection limits.

Water-Resources Investigations Report↗
USGS2021

Using fission-track radiography coupled with scanning electron microscopy for efficient identification of solid-phase uranium mineralogy at a former uranium pilot mill (Grand Junction, Colorado)

At a former uranium pilot mill in Grand Junction, Colorado, mine tailings and some subpile sediments were excavated to various depths to meet surface radiological standards, but residual solid-phase uranium below these excavation depths still occurs at concentrations above background. The combination of fission-track radiography and scanning electron microscope energy-dispersive X-ray spectroscopy (SEM-EDS) provides a uniquely efficient and quantitative way of determining mineralogic associations of uranium that can influence uranium mobility. After the creation of sample thin sections, a mica sheet is placed on those thin sections and irradiated in a nuclear research reactor. Decay of the irradiated uranium creates fission tracks that can be viewed with a microscope. The fission-track radiography images indicate thin section sample areas with elevated uranium that are focus areas for SEM-EDS work. EDS spectra provide quantitative elemental data that indicate the mineralogy of individual grains or grain coatings associated with the fission-track identification of elevated uranium. For the site in this study, the results indicated that uranium occurred (1) with coatings of aluminum–silicon (Al/Si) gel and gypsum, (2) dispersed in the unsaturated zone associated with evaporite-type salts, and (3) sorbed onto organic carbon. The Al/Si gel likely formed when low-pH waters were precipitated during calcite buffering, which in turn retained or precipitated trace amounts of Fe, As, U, V, Ca, and S. Understanding these mechanisms can help guide future laboratory and field-scale efforts in determining long-term uranium release rates to groundwater.

Colorado↗
USGS2024

In situ lung dust analysis by automated Field Emission Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy: A method for assessing inorganic particles in tissue from coal miners

Context.— Overexposure to respirable coal mine dust can cause severe lung disease including progressive massive fibrosis (PMF). Field emission scanning electron microscopy with energy dispersive x-ray spectroscopy (FESEM-EDS) has been used for in situ lung dust particle analysis for evaluation of disease etiology. Automating such work can reduce time, costs, and user bias. Objective.— To develop and test an automated FESEM-EDS method for in situ analysis of inorganic particles in coal miner lung tissue. Design.— We programmed an automated FESEM-EDS procedure to collect particle size and elemental data, using lung tissue from 10 underground coal miners with PMF and 4 control cases. A statistical clustering approach was used to establish classification criteria based on particle chemistry. Data were correlated to PMF/non-PMF areas of the tissue, using corresponding brightfield microscopy images. Results for each miner case were compared with a separate corresponding analysis of particles recovered following tissue digestion. Results.— In situ analysis of miner tissues showed higher particle number densities than controls and densities were generally higher in PMF than non-PMF areas. Particle counts were typically dominated by aluminum silicates with varying percentages of silica. Compared to digestion results for the miner tissues, in situ results indicated lower density of particles (number per tissue volume), larger size, and a lower ratio of silica to total silicates—probably due to frequent particle clustering in situ. Conclusions.— Automated FESEM-EDS analysis of lung dust is feasible in situ and could be applied to a larger set of mineral dust–exposed lung tissues to investigate specific histologic features of PMF and other dust-related occupational diseases.

Archives of Pathology↗
USGS1988

Detection of parvoviruses in wolf feces by electron microscopy

One hundred fifteen wolf (Canis lupus) feces were collected between 1980 and 1984 from northeastern Minnesota and were examined for canine parvovirus by negative contrast electron microscopy. Of these, seven (6%) samples revealed the presence of parvovirus. Some of these viruses were able to grow in cell cultures forming intranuclear inclusion bodies and giant cells.

Journal of Wildlife Diseases↗
USGS1991

Boron analysis by electron microprobe using MoB4C layered synthetic crystals

Preliminary electron microprobe studies of B distribution in minerals have been carried out using MoB4C-layered synthetic crystals to improve analytical sensitivity for B. Any microprobe measurements of the B contents of minerals using this crystal must include analyses for Cl to assess and correct for the interference of Cl X-rays on the BK?? peak. Microprobe analyses for B can be made routinely in tourmaline and other B-rich minerals, and minor B contents also can be determined in common rock-forming minerals. Incorporation of unusually high B contents in minerals other than borosilicates has been discovered in prograde and retrograde minerals in tourmalinites from the Broken Hill district, Australia, and may reflect high B activities produced during the metamorphism of tourmaline-rich rocks. -from Authors

American Mineralogist↗
USGS2004

Scanning electron microscopy investigations of laboratory-grown gas clathrate hydrates formed from melting ice, and comparison to natural hydrates

Scanning electron microscopy (SEM) was used to investigate grain texture and pore structure development within various compositions of pure sI and sII gas hydrates synthesized in the laboratory, as well as in natural samples retrieved from marine (Gulf of Mexico) and permafrost (NW Canada) settings. Several samples of methane hydrate were also quenched after various extents of partial reaction for assessment of mid-synthesis textural progression. All laboratory-synthesized hydrates were grown under relatively high-temperature and high-pressure conditions from rounded ice grains with geometrically simple pore shapes, yet all resulting samples displayed extensive recrystallization with complex pore geometry. Growth fronts of mesoporous methane hydrate advancing into dense ice reactant were prevalent in those samples quenched after limited reaction below and at the ice point. As temperatures transgress the ice point, grain surfaces continue to develop a discrete "rind" of hydrate, typically 5 to 30 ??m thick. The cores then commonly melt, with rind microfracturing allowing migration of the melt to adjacent grain boundaries where it also forms hydrate. As the reaction continues under progressively warmer conditions, the hydrate product anneals to form dense and relatively pore-free regions of hydrate grains, in which grain size is typically several tens of micrometers. The prevalence of hollow, spheroidal shells of hydrate, coupled with extensive redistribution of reactant and product phases throughout reaction, implies that a diffusion-controlled shrinking-core model is an inappropriate description of sustained hydrate growth from melting ice. Completion of reaction at peak synthesis conditions then produces exceptional faceting and euhedral crystal growth along exposed pore walls. Further recrystallization or regrowth can then accompany even short-term exposure of synthetic hydrates to natural ocean-floor conditions, such that the final textures may closely mimic those observed in natural samples of marine origin. Of particular note, both the mesoporous and highly faceted textures seen at different stages during synthetic hydrate growth were notably absent from all examined hydrates recovered from a natural marine-environment setting.

American Mineralogist↗
USGS2005

Scanning electron microscope studies of some early Miocene diatoms from the equatorial Pacific Ocean with descriptions of two new species, Actinocyclus jouseae Barron and Actinocyclus nigriniae Barron

Scanning electron microscope (SEM) and light microscope (LM) studies are used to propose and describe two new species, Actinocyclus jouseae Barron , sp. nov. and Actinocyclus nigriniae Barron , sp. nov. from lower Miocene sediments from equatorial Pacific ODP Site 1219. Parallel SEM and LM studies reveal that Thalassiosira bukryi Barron should be transferred to Azpeitia and suggest that Actinocyclus barronii Radionova is likely to be a variety of A. radionovae Barron

Proceedings of the California Academy of Sciences ↗
USGS1974

Energy dispersive spectrometry for quantitative mineralogical analyses: An ancillary system on an electron microphobe

Investigation of the Li-drifted Si-semiconductor X-ray detector for quantitative elemental analysis of some common rock-forming minerals shows that amounts of certain major elements having K spectra in the energy range of about 1.74 (Si) to 8.64 (Zn) kiloelectronvolts may be accurately determined, if spectral interferences are absent. Elements in major concentrations between 0.5 and 1.00 percent may be analyzed quantitatively without corrections of K spectra X-ray intensities when reference standards of similar composition are used and significant K spectra interferences between two adjacent elements are absent. Elemental concentrations less than about 0.5 weight percent cannot be precisely determined from raw X-ray intensity data owing to high and variable spectral background. Data show that spectral background corrections are feasible because spectral background is a linear function for the light-element oxides and silicates. Simultaneous quantitative elemental analysis, with both the energy dispersive spectrometer and the conventional wavelength dispersive spectrometers on the electron microprobe, is feasible.

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