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Mark Engle

Publications and source records attributed to Mark Engle.

6 recordsLinked to original sources

Compositional analysis of formation water geochemistry and microbiology of commercial and carbon dioxide-rich wells in the southwestern United States

Studies of naturally occurring subsurface carbon dioxide (CO 2 ) accumulations can provide useful information for potential CO 2 injection projects; however, the microbial communities and formation water geochemistry of most reservoirs are understudied. Formation water and microbial biomass were sampled at four CO 2 -rich reservoir sites: two within Bravo Dome, a commercial CO 2 field in New Mexico; one northwest of Bravo Dome in Colorado (Oakdale Field); and one southwest of Bravo Dome in New Mexico (Rafter “K” Ranch). Aside from the Rafter “K” Ranch site, minor differences were observed in the geochemistry of formation water collected from these sites compared to historical data. No organisms were significantly associated with Oakdale Field compared to the other three sites, nor were any hydrogeochemical or gas geochemical parameters (for example, CO 2 concentration) found to have significant associations with the microbial ecology of these four sites. Microorganisms from these sites were metabolically diverse and had the potential to (1) generate methane, (2) produce corrosive hydrogen sulfide (H 2 S), and (3) rapidly biofoul and (or) clog pore spaces by shifting microbial communities with changes in salinity or nutrient supply. This study demonstrates that high concentrations of CO 2 in subsurface reservoirs apparently have not imparted a distinct geochemical or microbiological signature on the associated formation waters and that the microorganisms in these reservoirs are metabolically diverse and could adapt to geochemical changes in the subsurface.

Colorado, New Mexico, Texas, Oklahoma

Direct trace element determination in oil and gas produced waters with inductively coupled plasma - Optical emission spectrometry (ICP-OES): Advantages of high salinity tolerance

Waters co-produced during petroleum extraction are the largest waste stream from oil and gas development. Reuse or disposal of these waters is difficult due to their high salinities and the sheer volumes generated. Produced waters may also contain valuable mineral commodities. While an understanding of produced water trace element composition is required for evaluating the associated resource and waste potential of these materials, measuring trace elements in brines is challenging due to the dilution requirements of typical methods. Alternatively, inductively coupled plasma-optical emission spectrometry (ICP-OES) has shown promise as being capable of direct measurements of trace elements within produced waters with minimal dilution. Here we evaluate direct ICP-OES trace element quantification in produced waters for 17 trace elements (As, Al, Ba, Be, Cd, Cr, Co, Cu, Hg, Mo, Ni, Pb, Rb, Sb, U, V, and Zn) within 15 produced waters from five U.S. continuous reservoirs. The ICP-OES results are compared against trace element levels determined using inductively coupled plasma-mass spectrometry from the same samples. Our results demonstrate the potential for direct analysis of high salinity waters using ICP-OES with minimal dilution and provide trace element concentrations in waters from several important U.S. petroleum-generating reservoirs where available data is sparse.

Montana, New York, North Dakota, Ohio, Pennsylvani

Pore characteristics of Wilcox Group Coal, U.S. Gulf Coast Region: Implications for the occurrence of coalbed gas

Pore characteristics of 27 subbituminous coal samples (16 mesh splits) from the Paleocene–Eocene Wilcox Group of north Louisiana (Ouachita and Caldwell Parishes) and south Texas (Zavala County) were examined in relation to desorbed gas content. Coal gas of the Wilcox Group is primarily biogenic in origin; thermogenic gas also may be present in some areas. On an as-received basis, desorbed gas contents range from 0.59 to 1.28 m 3 /t for Ouachita Parish samples, 0.37 to 5.19 m 3 /t for the Caldwell Parish samples, and 0.02 to 0.06 m 3 /t for the Zavala County samples. For Louisiana coal samples, micropore surface area and volume are correlated to the desorbed gas content of the Wilcox Group coal (correlations: r = 0.50 and 0.47, respectively), suggesting that micropore surface area and volume are important in terms of gas-holding capacity. Adsorption by micropores appears to be the primary form of gas storage for the Louisiana coal samples. Micropore surface area and volumes also are strongly correlated with the carbon/ash yield ratio (r = 0.97 and 0.94, respectively), indicating that gas sorption occurs primarily on organic matter. Mineral matter appears to reduce the sorption capacity of the coal. Micropore width decreases with depth (r = − 0.63), probably as the result of increasing pressure and coal rank with depth. For the Louisiana coal samples, mesopore surface area is negatively correlated with the carbon/ash yield ratio (r = − 0.70), suggesting that mesopores are preferentially associated with mineral matter. Average mesopore size is correlated with desorbed gas (r = 0.80) for the relatively shallow Ouachita Parish samples (average depth = 441 m, 1446 ft); these results suggest that the permeability of the Wilcox coal is greater in the shallow stratigraphic intervals compared to deeper intervals. Additionally, mesopore size decreases with depth (r = − 0.80). For Ouachita Parish coal samples, negative correlations of gas with mesopore surface area (r = − 0.74) and mesopore volume (r = − 0.56) strongly suggest that gas is not adsorbed in mesopores, and that free gas may be present in larger mesopores, macropores, or fractures of the Wilcox coal. Results also suggest that moisture in Ouachita Parish samples is present in mesopores; moisture in mesopores may have blocked gas adsorption. The low-gas south Texas samples (average depth = 313 m, 1026 ft) are markedly different from the Louisiana samples. Specifically, micropore surface area and micropore volume are negatively correlated with desorbed gas for the Texas samples (r =− 0.21 and − 0.36, respectively). Geologic or environmental conditions probably were not conducive to the generation or storage of microbial gas in the Zavala County coals. The geologic settings (i.e., salinity of formation water, groundwater recharge, permeability of coal) of each study area are important factors that need to be considered in relation to the potential for generation or storage of microbial gas. In south Texas, tectonic stress may have led to a reduction in permeability in the Wilcox Group coal, creating an unfavorable environment for the generation or preservation of microbial gas. The subbituminous rank of the Zavala coals is also too low for significant thermogenic gas generation to have occurred.

Arkansas, Louisiana, Mississippi, Texas

Discharges of produced waters from oil and gas extraction via wastewater treatment plants are sources of disinfection by-products to receiving streams

Fluids co-produced with oil and gas production (produced waters) are often brines that contain elevated concentrations of bromide. Bromide is an important precursor of several toxic disinfection by-products (DBPs) and the treatment of produced water may lead to more brominated DBPs. To determine if wastewater treatment plants that accept produced waters discharge greater amounts of brominated DBPs, water samples were collected in Pennsylvania from four sites along a large river including an upstream site, a site below a publicly owned wastewater treatment plant (POTW) outfall (does not accept produced water), a site below an oil and gas commercial wastewater treatment plant (CWT) outfall, and downstream of the POTW and CWT. Of 29 DBPs analyzed, the site at the POTW outfall had the highest number detected (six) ranging in concentration from 0.01 to 0.09 μg L − 1 with a similar mixture of DBPs that have been detected at POTW outfalls elsewhere in the United States. The DBP profile at the CWT outfall was much different, although only two DBPs, dibromochloronitromethane (DBCNM) and chloroform, were detected, DBCNM was found at relatively high concentrations (up to 8.5 μg L − 1 ). The water at the CWT outfall also had a mixture of inorganic and organic precursors including elevated concentrations of bromide (75 mg L − 1 ) and other organic DBP precursors (phenol at 15 μg L − 1 ). To corroborate these DBP results, samples were collected in Pennsylvania from additional POTW and CWT outfalls that accept produced waters. The additional CWT also had high concentrations of DBCNM (3.1 μg L − 1 ) while the POTWs that accept produced waters had elevated numbers (up to 15) and concentrations of DBPs, especially brominated and iodinated THMs (up to 12 μg L − 1 total THM concentration). Therefore, produced water brines that have been disinfected are potential sources of DBPs along with DBP precursors to streams wherever these wastewaters are discharged.

Science of the Total Environment

Health effects of energy resources

Energy resources (coal, oil, and natural gas) are among the cornerstones of modern industrial society. The exploitation of these resources, however, is not without costs. Energy materials may contain harmful chemical substances that, if mobilized into air, water, or soil, can adversely impact human health and environmental quality. In order to address the issue of human exposure to toxic substances derived from energy resources, the U.S. Geological Survey (USGS) Energy Resources Program developed a project entitled 'Impacts of Energy Resources on Human Health and Environmental Quality.' The project is intended to provide policymakers and the public with the scientific information needed to weigh the human health and environmental consequences of meeting our energy needs. This fact sheet discusses several areas where the USGS Energy Resources Program is making scientific advances in this endeavor.

Fact Sheet

Emissions from coal fires and their impact on the environment

Self-ignited, naturally occurring coal fires and fires resulting from human activities persist for decades in underground coal mines, coal waste piles, and unmined coal beds. These uncontrolled coal fires occur in all coal-bearing parts of the world (Stracher, 2007) and pose multiple threats to the global environment because they emit greenhouse gases - carbon dioxide (CO 2 ), and methane (CH 4 ) - as well as mercury (Hg), carbon monoxide (CO), and other toxic substances (fig. 1). The contribution of coal fires to the global pool of atmospheric CO 2 is little known but potentially significant. For China, the world's largest coal producer, it is estimated that anywhere between 10 million and 200 million metric tons (Mt) of coal reserves (about 0.5 to 10 percent of production) is consumed annually by coal fires or made inaccessible owing to fires that hinder mining operations (Rosema and others, 1999; Voigt and others, 2004). At this proportion of production, coal amounts lost to coal fires worldwide would be two to three times that for China. Assuming this coal has mercury concentrations similar to those in U.S. coals, a preliminary estimate of annual Hg emissions from coal fires worldwide is comparable in magnitude to the 48 tons of annual Hg emissions from all U.S. coal-fired power-generating stations combined (U.S. Environmental Protection Agency, 2002). In the United States, the combined cost of coal-fire remediation projects, completed, budgeted, or projected by the U.S. Department of the Interior's Office of Surface Mining Reclamation and Enforcement (OSM), exceeds $1 billion, with about 90% of that in two States - Pennsylvania and West Virginia (Office of Surface Mining Enforcement and Reclamation, 2008; fig. 2). Altogether, 15 States have combined cumulative OSM coal-fire project costs exceeding $1 million, with the greatest overall expense occurring in States where underground coal fires are predominant over surface fires, reflecting the greater cost of extinguishing underground fires (fig. 2) (see 'Controlling Coal Fires'). In this fact sheet we review how coal fires occur, how they can be detected by airborne and remote surveys, and, most importantly, the impact coal-fire emissions may have on the environment and human health. In addition, we describe recent efforts by the U.S. Geological Survey (USGS) and collaborators to measure fluxes of CO 2 , CO, CH 4 , and Hg, using groundbased portable detectors, and combining these approaches with airborne thermal imaging and CO 2 measurements. The goal of this research is to develop approaches that can be extrapolated to large fires and to extrapolate results for individual fires in order to estimate the contribution of coal fires as a category of global emissions.

Fact Sheet