Geology topics

Geoffrey S. Plumlee

Publications and source records attributed to Geoffrey S. Plumlee.

At least 55 records · Page 3Linked to original sources

USGS2010

Trace-metal concentrations in African dust: Effects of long-distance transport and implications for human health

The Sahara and Sahel lose billions of tons of eroded mineral soils annually to the Americas and Caribbean, Europe and Asia via atmospheric transport. African dust was collected from a dust source region (Mali, West Africa) and from downwind sites in the Caribbean [Trinidad-Tobago (TT) and U.S. Virgin Islands (VI)] and analysed for 32 trace-elements. Elemental composition of African dust samples was similar to that of average upper continental crust (UCC), with some enrichment or depletion of specific trace-elements. Pb enrichment was observed only in dust and dry deposition samples from the source region and was most likely from local use of leaded gasoline. Dust particles transported long-distances (VI and TT) exhibited increased enrichment of Mo and minor depletion of other elements relative to source region samples. This suggests that processes occurring during long-distance transport of dust produce enrichment/depletion of specific elements. Bioaccessibility of trace-metals in samples was tested in simulated human fluids (gastric and lung) and was found to be greater in downwind than source region samples, for some metals (e.g., As). The large surface to volume ratio of the dust particles (<2.5 µm) at downwind sites may be a factor.

Bamako, Emetteur Kati, Flagstaff Hill, St. Croix, ↗

USGS2009

Spectroscopic and x-ray diffraction analyses of asbestos in the World Trade Center dust: Asbestos content of the settled dust

On September 17 and 18, 2001, samples of settled dust and airfall debris were collected from 34 sites within a 1-km radius of the WTC collapse site, including a sample from an indoor location unaffected by rainfall, and samples of insulation from two steel beams at Ground Zero. Laboratory spectral and x-ray diffraction analyses of the field samples detected trace levels of serpentine minerals, including chrysotile asbestos, in about two-thirds of the dust samples at concentrations at or below ~1 wt%. One sample of a beam coating material contained up to 20 wt% chrysotile asbestos. Analyses indicate that trace levels of chrysotile were distributed with the dust radially to distances greater than 0.75 km from Ground Zero. The chrysotile content of the dust is variable and may indicate that chrysotile asbestos was not distributed uniformly during the three collapse events.

New York↗

USGS2009

Environmental mapping of the World Trade Center area with imaging spectroscopy after the September 11, 2001 attack

The Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) was flown over the World Trade Center area on September 16, 18, 22, and 23, 2001. The data were used to map the WTC debris plume and its contents, including the spectral signatures of asbestiform minerals. Samples were collected and used as ground truth for the AVARIS mapping. A number of thermal hot spots were observed with temperatures greater than 700 °C. The extent and temperatures of the fires were mapped as a function of time. By September 23, most of the fires observed by AVIRIS had been eliminated or reduced in intensity. The mineral absorption features mapped by AVARIS only indicated the presence of serpentine mineralogy and not if the serpentine has asbestiform.

Book chapter↗

USGS2009

Materials characterization of dusts generated by the collapse of the World Trade Center

The major inorganic components of the dusts generated from the collapse of the World Trade Center buildings on September 11, 2001 were concrete materials, gypsum, and man-made vitreous fibers. These components were likely derived from lightweight Portland cement concrete floors, gypsum wallboard, and spray-on fireproofing and ceiling tiles, respectively. All of the 36 samples collected by the USGS team had these materials as the three major inorganic components of the dust. Components found at minor and trace levels include chrysotile asbestos, lead, crystalline silica, and particles of iron and zinc oxides. Other heavy metals, such as lead, bismuth, copper, molybdenum, chromium, and nickel, were present at much lower levels occurring in a variety of chemical forms. Several of these materials have health implications based on their chemical composition, morphology, and bioaccessibility.

Book chapter↗

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↗

USGS2009

Questa baseline and pre-mining ground-water quality investigation, 7. A pictorial record of chemical weathering, erosional processes, and potential debris-flow hazards in scar areas developed on hydrothermally altered rocks

Erosional scar areas developed along the lower Red River basin, New Mexico, reveal a complex natural history of mineralizing processes, rapid chemical weathering, and intense physical erosion during periodic outbursts of destructive, storm-induced runoff events. The scar areas are prominent erosional features with craggy headwalls and steep, denuded slopes. The largest scar areas, including, from east to west, Hottentot Creek, Straight Creek, Hansen Creek, Lower Hansen Creek, Sulfur Gulch, and Goat Hill Gulch, head along high east-west trending ridges that form the northern and southern boundaries of the lower Red River basin. Smaller, topographically lower scar areas are developed on ridge noses in the inner Red River valley. Several of the natural scar areas have been modified substantially as a result of large-scale open-pit and underground mining at the Questa Mine; for example, much of the Sulfur Gulch scar was removed by open pit mining, and several scars are now partially or completely covered by mine waste dumps.

New Mexico↗

USGS2009

Sample collection of ash and burned soils from the October 2007 southern California Wildfires

Between November 2 through 9, 2007 scientists from the U.S. Geological Survey (USGS) collected samples of ash and burned soils from 28 sites in six areas burned as a result of the Southern California wildfires of October 2007, including the Harris, Witch, Santiago, Ammo, Canyon, and Grass Valley Fires. The primary goal of this sampling and analysis effort was to understand how differences in ash and burned soil composition relate to vegetation type, underlying bedrock geology, burn intensity, and residential versus wildland. Sampling sites were chosen with the input of local experts from the USGS Water Resources and Biological Resources Disciplines to help understand possible effects of the fires on water supplies, ecosystems, and endangered species. The sampling was also carried out in conjunction with detailed field analysis of the spectral reflectance characteristics of the ash, so that chemical and mineralogical characteristics of the field samples could be used to help interpret data collected as part of an airborne, hyperspectral remote-sensing survey of several of the burned areas in mid-late November, 2007. This report presents an overview of the field sampling methodologies used to collect the samples, includes representative photos of the sites sampled, and summarizes important characteristics of each of the collection sites. In this report we use the term “ash” to refer collectively to white mineral ash, which results from full combustion of vegetation and black charred organic matter from partial combustion of vegetation or other materials. These materials were found to be intermingled as a deposited residue on the soil surface following the Southern California fires of 2007.

Open-File Report↗

USGS2009

Climax-type porphyry molybdenum deposits

Climax-type porphyry molybdenum deposits, as defined here, are extremely rare; thirteen deposits are known, all in western North America and ranging in age from Late Cretaceous to mainly Tertiary. They are consistently found in a postsubduction, extensional tectonic setting and are invariably associated with A-type granites that formed after peak activity of a magmatic cycle. The deposits consist of ore shells of quartz-molybdenite stockwork veins that lie above and surrounding the apices of cupola-like, highly evolved, calc-alkaline granite and subvolcanic rhyolite-porphyry bodies. These plutons are invariably enriched in fluorine (commonly >1 percent), rubidium (commonly >500 parts per million), and niobium-tantalum (Nb commonly >50 parts per million). The deposits are relatively high grade (typically 0.1-0.3 percent Mo) and may be very large (typically 100-1,000 million tons). Molybdenum, as MoS2, is the primary commodity in all known deposits. The effect on surface-water quality owing to natural influx of water or sediment from a Climax-type mineralized area can extend many kilometers downstream from the mineralized area. Waste piles composed of quartz-silica-pyrite altered rocks will likely produce acidic drainage waters. The potential exists for concentrations of fluorine or rare metals in surface water and groundwater to exceed recommended limits for human consumption near both mined and unmined Climax-type deposits.

Open-File Report↗

USGS2009

Report from Ground Zero: How geoscientists aid in the aftermath of environmental disasters

People around the world remember when they first learned of the attacks on New York City’s World Trade Center towers on Sept. 11, 2001. For me, the memories are vivid — my feelings of shock, horror and sadness were similarly etched on the faces of all the attendees of a mining and the environment workshop in Buenos Aires, Argentina, where I was speaking. At that time, I had no idea that our small research group at the U.S. Geological Survey in Denver, Colo., would soon be called upon to help public officials understand the potential health and environmental implications of the disaster and the ensuing rescue, recovery and cleanup efforts.

Earth Magazine↗

USGS2008

Preliminary analytical results for a mud sample collected from the LUSI Mud Volcano, Sidoarjo, East Java, Indonesia

On May 29, 2006, mud and gases began erupting unexpectedly from a vent 150 meters away from a hydrocarbon exploration well near Sidoarjo, East Java, Indonesia. The eruption, called the LUSI (Lumpur 'mud'-Sidoarjo) mud volcano, has continued since then at rates as high as 160,000 m3 per day. At the request of the United States Department of State, the U.S. Geological Survey (USGS) has been providing technical assistance to the Indonesian Government on the geological and geochemical aspects of the mud eruption. This report presents initial characterization results of a sample of the mud collected on September 22, 2007, as well as inerpretive findings based on the analytical results. The focus is on characteristics of the mud sample (including the solid and water components of the mud) that may be of potential environmental or human health concern. Characteristics that provide insights into the possible origins of the mud and its contained solids and waters have also been evaluated.

East Java↗

USGS2008

Leachate Geochemical Results for Ash and Burned Soil Samples from the October 2007 Southern California Wildfires

This report is the second release of leachate geochemical data included as part of a multidisciplinary study of ash and burned soil samples from the October 2007 wildfires in southern California. Geochemical data for the first set of samples were released in an Open-File Report (Plumlee and others, 2007). This study is a continuation of that work. The objectives of this leaching study are to aid in understanding the interactions of ash and burned soil with rainfall. For this study, 12 samples collected in early November 2007 were leached using the U.S. Geological Survey (USGS) Field Leach Test (FLT). Following leaching, sub-samples of the leachate were analyzed for pH and specific conductance. The leachate was then filtered, and aliquots were preserved for geochemical analysis. This report presents leachate geochemical data for pH, specific conductance, alkalinity, anions using ion chromatography (I.C.), cations using inductively coupled plasma?atomic mass spectrometry (ICP-MS), and mercury by continuous flow injection?cold vapor?atomic fluorescence (CVAFS).

Open-File Report↗

USGS2008

Leachate Geochemical Results for Ash Samples from the June 2007 Angora Wildfire Near Lake Tahoe in Northern California

This report releases leachate geochemical data for ash samples produced by the Angora wildfire that burned from June 24 to July 2, 2007, near Lake Tahoe in northern California. The leaching studies are part of a larger interdisciplinary study whose goal is to identify geochemical characteristics and properties of the ash that may adversely affect human health, water quality, air quality, animal habitat, endangered species, debris flows, and flooding hazards. The leaching study helps characterize and understand the interactions that occur when the ash comes in contact with rain or snowmelt, and helps identify the constituents that may be mobilized as run-off from these materials. Similar leaching studies were conducted on ash and burned soils from the October 2007 southern California wildfires (Hageman and others, 2008; Plumlee and others, 2007).

Open-File Report↗

USGS2008

Release of Hexavalent Chromium by Ash and Soils in Wildfire-Impacted Areas

The highly oxidizing environment of a wildfire has the potential to convert any chromium present in the soil or in residential or industrial debris to its more toxic form, hexavalent chromium, a known carcinogen. In addition, the highly basic conditions resulting from the combustion of wood and wood products could result in the stabilization of any aqueous hexavalent chromium formed. Samples were collected from the October 2007 wildfires in Southern California and subjected to an array of test procedures to evaluate the potential effects of fire-impacted soils and ashes on human and environmental health. Soil and ash samples were leached using de-ionized water to simulate conditions resulting from rainfall on fire-impacted areas. The resulting leachates were of high pH (10-13) and many, particularly those of ash from burned residential areas, contained elevated total chromium as much as 33 micrograms per liter. Samples were also leached using a near-neutral pH simulated lung fluid to model potential chemical interactions of inhaled particles with fluids lining the respiratory tract. High Performance Liquid Chromatography coupled to Inductively Coupled Plasma Mass Spectrometry was used to separate and detect individual species (for example, Cr+3, Cr+6, As+3, As+5, Se+4, and Se+6). These procedures were used to determine the form of the chromium present in the de-ionized water and simulated lung fluid leachates. The results show that in the de-ionized water leachate, all of the chromium present is in the form of Cr+6, and the resulting high pH tends to stabilize Cr+6 from reduction to Cr+3. Analysis of the simulated lung fluid leachates indicates that the predominant form of chromium present in the near-neutral pH of lung fluid would be Cr+6, which is of concern due to the high possibility of inhalation of the small ash and soil particulates, particularly by fire or restoration crews.

Open-File Report↗

USGS2008

Speciation Methods Used to Assess Potential Health Effects of Toxic Metals in Environmental Materials

Assessing potential exposures to toxic metals or metalloids such as arsenic and chromium in environmental materials is important in protecting public health. The chemical form of an element in, or released from, a material is also important, since some forms, such as Cr(VI), are more toxic than others, for example, Cr(III). We have used a variety of procedures to assess potential exposures to hexavalent chromium in ash and burned soils from October 2007 southern California wildfires. Synthetic lung-fluid and de-ionized water extractions simulate release in the lungs and potential environmental releases due to rainfall. Extracts were analyzed for specific chromium and arsenic species using HPLC-ICP-MS methodology. Results indicate that the highly oxidizing environment in wildfires promotes some chromium conversion to Cr(VI), and that the caustic alkalinity of ash enhances Cr(VI) release and stability in lung fluids and rainfall.

Open-File Report↗

USGS2007

Characterization of flood sediments from Hurricanes Katrina and Rita and potential implications for human health and the environment

The flooding in the greater New Orleans, La., area that resulted from Hurricanes Katrina and Rita in August and September 2005 left behind accumulations of sediments up to many centimeters thick on streets, lawns, parking lots, and other flat surfaces (fig. 1). During the flood dewatering and subsequent cleanup, there were concerns that these sediments might contain pathogens and chemical contaminants that would pose a health risk to emergency responders, cleanup workers, and local residents who came into contact with the wet sediments or inhaled dusts generated from dried sediments. In response to these concerns, U.S. Geological Survey (USGS) scientists and colleagues characterized the potential environmental and health hazards of hurricane flood sediments from the greater New Orleans and Slidell, La., area.

Louisiana↗

USGS2007

Preliminary analytical results for ash and burned soils from the October 2007 southern California wildfires

The U.S. Geological Survey (USGS) collected ash and burned soils from about 28 sites in southern California wildfire areas (Harris, Witch, Ammo, Santiago, Canyon and Grass Valley) from Nov. 2 through 9, 2007 (table 1). USGS researchers are applying a wide variety of analytical methods to these samples, with the goal of helping identify characteristics of the ash and soils from wildland and suburban burned areas that may be of concern for their potential to adversely affect water quality, human health, endangered species, and debris-flow or flooding hazards. These studies are part of the Southern California Multi-Hazards Demonstration Project, and preliminary findings are presented here.

Open-File Report↗

USGS2006

The toxicological geochemistry of Earth materials: An overview of processes and the interdisciplinary methods used to understand them

A broad spectrum of earth materials have been linked to, blamed for, and/or debated as sources for disease. In some cases, the links are clear. For example, excessive exposures to mineral dusts have long been recognized for their role in diseases such as: asbestosis, mesothelioma, and lung cancers (asbestos); silicosis and lung cancer (silica dusts); and coal-workers pneumoconiosis (coal dust). Lead poisoning, particularly in toddlers and young children, has been conclusively linked to involuntary ingestion of soils or other materials contaminated with lead-rich paint particles, leaded gasoline combustion byproducts, and some types of lead-rich mine wastes or smelter particulates. Waters with naturally elevated arsenic contents are common in many regions of the globe, and consumption of these waters has been documented as the source of arsenic-related diseases affecting thousands of people in south Asia and other regions. Exposure to dusts or soils containing pathogens has been documented as the cause of regionally common diseases such as valley fever (coccidioidomycosis) and much rarer diseases such as anthrax. Links between many other earth materials and specific diseases, although suspected, are less clear or are debated. For example, it has been suggested that geographic clusters of diseases such as leukemia are related to exposures to waters or atmospheric particulates containing organic or metal contaminants; however, for many clusters the exact causal relationships between disease and environmental exposure are difficult to prove conclusively. Even for many diseases in which the causal relationship is clear, such as in asbestosis and mesothelioma triggered by asbestos exposure, the minimum exposures needed to trigger disease, the influence of genetic factors, and the exact mechanisms of toxicity are still incompletely understood and are the focus of considerable debate within the public health community. Hence, understanding the health effects resulting from occupational and environmental exposures to a wide variety of earth materials remains a very active and fruitful area of research.

Reviews in Mineralogy and Geochemistry↗

USGS2006

USGS environmental characterization of flood sediments left in the New Orleans area after Hurricanes Katrina and Rita, 2005 — Progress Report

Introduction: The flooding in the greater New Orleans area that resulted from Hurricanes Katrina and Rita in September, 2005, left behind accumulations of sediments up to many centimeters thick on streets, lawns, parking lots, and other flat surfaces. These flood sediment deposits have been the focus of extensive study by the US Environmental Protection Agency (EPA) and Louisiana Department of Environmental Quality (LDEQ) due to concerns that the sediments may contain elevated levels of heavy metals, organic contaminants, and microbes. The U.S. Geological Survey (USGS) is characterizing a limited number of flood sediment samples that were collected on September 15-16 and October 6-7, 2005, from the greater New Orleans area by personnel from the USGS Louisiana Water Science Center in Baton Rouge. Small samples (< 3 pints each) of wet to dry flood sediment were collected from 11 localities around downtown New Orleans on September 15, 2005, and two large samples (40 pints each) of wet flood sediment were collected from the Chalmette area on September 16. Twelve additional samples (8-10 pints each) were collected from New Orleans, Slidell, Rigolets, and Violet on October 6 and 7. The USGS characterization studies of these flood sediments are designed to produce data and interpretations regarding how the sediments and any contained contaminants may respond to environmental processes. This information will be of use to cleanup managers and DoI/USGS scientists assessing environmental impacts of the hurricanes and subsequent cleanup activities.

Louisiana↗