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At least 73 records · Page 4Linked to original sources
USGS2018

Suppression of vitrinite reflectance by bitumen generated from liptinite during hydrous pyrolysis of artificial source rock

Mean random vitrinite reflectance (R o ) is the most widely accepted method to determine thermal maturity of coal and other sedimentary rocks. However, oil-immersion R o of polished rock or kerogen samples is commonly lower than R o values measured in samples from adjacent vitrinite-rich coals that have undergone the same level of thermal stress. So-called suppressed R o values have also been observed in hydrous pyrolysis experiments designed to simulate petroleum formation. Various hypotheses to explain R o suppression, such as sorption of products generated from liptinite during maturation, diagenetic formation of perhydrous vitrinite or overpressure, remain controversial. To experimentally test for suppression of vitrinite reflectance, artificial rock was prepared using silica and a calcined blend of limestone and clay with various proportions of thermally immature vitrinite-rich Wyodak-Anderson coal and liptinite-rich kerogen isolated from the oil-prone Parachute Creek Member of the Green River Formation. The samples were subjected to hydrous pyrolysis for 72 h. at isothermal temperatures of 300 °C, 330 °C, and 350 °C to simulate burial maturation. Compared to artificial rock that contains only coal, samples with different proportions of oil-prone kerogen show distinct suppression of calibrated R o at 300 °C and 330 °C. The reflectance of solid bitumen generated during heating of the samples is lower than that of the associated vitrinite and does not interfere with the R o measurements. These results provide the first experimental evidence that R o suppression occurs in vitrinite mixed with liptinite-rich kerogen in a rock matrix. Although the precise chemical mechanism for R o suppression by liptinite remains unclear, free radicals generated from solid bitumen and associated volatile products during maturation of liptinite may contribute to termination reactions that slow the aromatization and rearrangement of polyaromatic sheets in vitrinite, thus suppressing R o . This mechanism does not preclude R o suppression that might result from overpressure or differences in redox conditions during diagenesis.

Organic Geochemistry↗
USGS2019

Reflectance increase from broad beam ion milling of coals and organic-rich shales due to increased surface flatness

Broad ion beam (BIB) milling is useful in organic petrology because it can yield flat sample surfaces and avert the ‘smearing’ of organic matter (OM) that results from traditional mechanical polishing. This potentially makes BIB especially useful in the study of nano-porosity, where even minor mechanical disruption of the sample surface distorts the sample characteristic of interest—the pore structure. However, several studies have observed an OM reflectance increase after BIB milling, concluding that ion milling may cause thermal alteration to OM surfaces. To better understand ion milling effects on organic matter, coal (subbituminous, high volatile bituminous, medium volatile bituminous, anthracite) and shale [Bakken Formation, Ohio Shale-Huron Member (5), Kimmeridge Clay Formation, Alum Shale, New Albany Shale] samples were prepared using traditional mechanical polishing methods. Reflectance measurements (% Ro) were gathered on all maceral types present before BIB milling, followed by re-measurement of OM reflectance at the same locations after milling. Most OM increased in reflectance after BIB milling, with some exceptions in high maturity samples. Liptinite macerals in both coal and shale samples showed the greatest percent reflectance increase on average (+133%; n=338), followed by solid bitumen (+49%; n=313), vitrinite (+26%; n=413), and inertinite (+9%; n=220). Despite the increases to OM reflectance caused by BIB milling, no evidence was found for kerogen conversion (e.g., change in maceral abundances), or for migration of newly generated petroleum (e.g., pseudomorphic replacement of kerogen by solid bitumen). Such changes occur when samples are thermally altered from immature conditions into the oil window (e.g., by hydrous pyrolysis), and, if the increases in OM reflectance were thermally driven (by BIB milling), they should have been observed in the above experiments. Herein, we also used atomic force microscopy to document a decrease in surface roughness of correlative locations of OM on pre- and post-ion milled samples. This improved surface polish caused by BIB milling appears to be the root cause of increased OM reflectance, as no other supporting evidence of thermal alteration could be found. That is, the fraction of light formerly lost to oblique scatter in diffuse reflectance from a mechanically polished surface is converted to specular reflectance after BIB ion milling. Thus the light leaves the surface at a near normal angle and returns to the detector, resulting in increased OM reflectance.

International Journal of Coal Geology↗
USGS1897

Eighteenth annual report of the United States Geological Survey to the Secretary of the Interior, 1896-1897: Part V - Mineral resources of the United States, 1896, nonmetallic products, except coal

In the preceding volumes of Mineral Resources the annual reports on the manufacture of coke a well a those on the production of crude petroleum and natural gas were prepared by Mr. Joseph Dame Weeks, of Pittsburg, Pa. The sudden death of Mr. Weeks on December 26, 1896, necessitated the distribution of the work formerly done by him among his former associates in the statistical division of the Geological Survey. The preparation of the report on the manufacture of coke for 1896 has accordingly devolved upon the writer. To have accepted such an undertaking under ordinary circumstance would have meant the entering upon a difficult task. In the matter of coke production it has been made comparatively easy by the thoroughness with which Mr. Weeks has already covered the ground. The work done by Mr. Week's in his report for the Tenth and Eleventh Censuses and the annual volume of Mineral Resources has left little for his successor but the continuation of the statistical tables and the preparation of such text as refers directly to them. Mr. Weeks, at the time of his death, had the work for collecting the statistics of coke production in 1896 well advanced, and the excellence of his system and methods have been shown in the fact that the work of collecting the statistics was carried out on his lines uninterruptedly.

Annual Report↗
USGS1996

Application of reflectance micro-Fourier Transform infrared analysis to the study of coal macerals: An example from the Late Jurassic to Early Cretaceous coals of the Mist Mountain Formation, British Columbia, Canada

The applicability of the reflectance micro-Fourier Transform infra-red spectroscopy (FTIR) technique for analyzing the distribution of functional groups in coal macerals is discussed. High quality of spectra, comparable to those obtained using other FTIR techniques (KBr pellet and transmission micro-FTIR), indicate this technique can be applied to characterizing functional groups under most conditions. The ease of sample preparation, the potential to analyze large intact samples, and ability to characterize organic matter in areas as small as 20 ??m are the main advantages of reflectance micro-FTIR. The quantitative aspects of reflectance micro-FTIR require further study. The examples from the coal seams of the Mist Mountain Formation, British Columbia show that at high volatile bituminous rank, reflectance micro-FTIR provides valuable information on the character of aliphatic chains of vitrinite and liptinite macerals. Because the character of aliphatic chains influences bond disassociation energies, such information is useful from a hydrocarbon generation viewpoint. In medium volatile bituminous coal liptinite macerals are usually not detectable but this technique can be used to study the degree of oxidation and reactivity of vitrinite and semifusinite.

International Journal of Coal Geology↗
USGS1981

Historical review of and current progress in coal-resource estimation in the United States

Nine estimates of the coal resources of the United States have been published in the past 71 years. Although many details of these estimates differ markedly, the 1913, 1922, and 1974 estimates are surprisingly similar. Some differences are due to increased geologic data, others reflect changes in terminology, definitions, criteria, guidelines, and methodologies used for estimating coal resources and reserves during the last 100 years. Because of the increased data and changes, many of the early estimates are not particularly useful in modern resource assessments. Preliminary definitions that are being prepared in 1980 by the U.S. Geological Survey are compared with those published in 1976 and currently in use. Anticipated results of the new definitions are to lessen existing confusion about estimation procedures, to make such procedures easier and more precise, and to promote use of a commonly accepted terminology accompanied by standardized definitions, criteria, guidelines, and methodologies for estimating coal resources.

Geological Society of America Bulletin↗
USGS2011

Measured reflectance suppressed by thin-film interference of crude oil smeared on glass - as on vitrinite in coal or petroliferous rocks

The tool of measuring "vitrinite reflectance" under a microscope has great value in petroleum exploration and coal utilization, and the reflectance is a simple number, such as 1.4% Ro, with some slight variations depending on technique. Sample collection, preparation and measurement are simple and many sedimentary rocks yield vitrinite. However, the reported number can lead one astray if its origin and quality are not fully understood. I analyze here just one factor, "smear" of crude oil on the polished surface (from the sample), which may reduce reflectance because of thin-film interference. Some other causes of error are listed in an addendum to this note.

Society for Organic Petrology Newsletter↗
USGS2000

High temperature hydrogen sulfide adsorption on activated carbon - I. Effects of gas composition and metal addition

Various types of activated carbon sorbents were evaluated for their ability to remove H2S from a simulated coal gas stream at a temperature of 550 ??C. The ability of activated carbon to remove H2S at elevated temperature was examined as a function of carbon surface chemistry (oxidation, thermal desorption, and metal addition), and gas composition. A sorbent prepared by steam activation, HNO3 oxidation and impregnated with Zn, and tested in a gas stream containing 0.5% H2S, 50% CO2 and 49.5% N2, had the greatest H2S adsorption capacity. Addition of H2, CO, and H2O to the inlet gas stream reduced H2S breakthrough time and H2S adsorption capacity. A Zn impregnated activated carbon, when tested using a simulated coal gas containing 0.5% H2S, 49.5% N2, 13% H2, 8.5% H2O, 21% CO, and 7.5% CO2, had a breakthrough time of 75 min, which was less than 25 percent of the length of breakthrough for screening experiments performed with a simplified gas mixture of 0.5% H2S, 50% CO2, and 49.5% N2.

Carbon↗
USGS2020

Sample mounting for organic petrology: No thermal effects from transient exposure to elevated temperatures

For sample mounting, organic petrology laboratories typically use cold-setting epoxy-resin (e.g., 40 °C, used by Oklahoma Geological Survey, OGS) or heat-setting thermoplastic (e.g., 180 °C, used by U.S. Geological Survey, USGS). Previous workers have suggested a systematic huminite/vitrinite reflectance (VR o ) increase was associated with the thermoplastic preparation process, relative to epoxy mounting, which was possibly attributed to moisture loss from organic matter due to the transient high temperatures of plastic mounting. In this study, we evaluated thermal effects to low thermal maturity organic matter from transient exposure to elevated temperatures. A subbituminous coal sample was subjected to long-term (4 to 38 weeks) exposure to temperatures of 85 to 120 °C and afterward evaluated by multiple approaches to test thermal advance [elemental analyses, Rock-Eval pyrolysis, Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), pyrolysis gas chromatography, and petrographic analyses, including huminite/vitrinite reflectance and spectral fluorescence], all of which showed no detectable systematic (statistically insignificant) changes between the original sample and its heat-treated products. We also compared huminite/vitrinite reflectance of six low thermal maturity samples (those most likely to react to transient heating) mounted via both cold-setting epoxy-resin and heat-setting thermoplastic. Results indicate measured VR o of a sample prepared by one mounting process was within the standard deviation of reflectance for the same sample prepared via the other process. Moreover, VR o results were not systematically higher in thermoplastic mounts. Contrary to previous work, these results suggest thermoplastic mounting or other transient exposure to elevated temperatures does not impact thermal maturity estimates from reflectance measurement for low thermal maturity organic samples. Furthermore, the average interlaboratory difference in measured VR o (between OGS and USGS) for the same sample prepared by either epoxy-resin or thermoplastic mounting was 0.038%, about double the average difference between VR o for the same sample prepared via epoxy-resin versus thermoplastic in a single laboratory (0.024%). This result indicates interlaboratory variability impacts VR o measurement reproducibility to the extent that systematic differences could not be observed between thermoplastic and cold-setting sample preparation approaches, even if such differences were present.

International Journal of Coal Geology↗
USGS2023

Evaluation of portable Raman spectroscopic analysis for source-rock thermal maturity assessments on bulk crushed rock

This study presents a simplified method and empirical relationships for determining organic matter thermal maturity using a portable Raman system equipped with a 785 nm laser, for analysis of crushed, whole-rock samples. Suites of rocks represented by shale and coal samples with various mineralogical composition, thermal maturity, and total organic carbon (TOC) were used to test the method and build correlations between Raman band separation (RBS) values and traditional thermal maturity indicators, organic matter reflectance (Ro), and programmed temperature pyrolysis (Tmax) values. A set of disparate shale samples, where both vitrinite and solid bitumen reflectance values were reported, have Ro values that range from 0.40 to 4.62%. Above 3.35% Ro, the corresponding RBS values plateau at ∼290 cm−1, thus correlations were evaluated with a linear regression (R2 = 0.96) between 0.40 and 3.35% Ro. Shale samples with Ro < 2% and Tmax < 551 were also used to correlate Tmax and RBS, yielding a linear correlation with an R2 of 0.94. For the coal data set, Ro values range from 1.21 to 4.08% and correlated RBS values plateau at ∼250 cm−1 above Ro = 3.0%, suggesting its correlative application below this maturity level. Several sample preparation methods were tested on cuttings material and standard deviation values for RBS were minimized by washing, drying, and hand crushing the material to pass through a 40-mesh sieve, although less preparation can still yield reliable results. The high degrees of correlation between whole-rock RBS data and two thermal maturity indicators demonstrate the utility of this approach for generating source rock thermal maturity data from minimally processed, whole-rock samples which could easily be applied in field or laboratory settings.

International Journal of Coal Geology↗
USGS2001

Chemotaxonomy for naturally macerated tree-fern cuticles (Medullosales and Marattiales), Carboniferous Sydney and Mabou Sub-Basins, Nova Scotia, Canada

Naturally macerated cuticles (NMC) and one synangium, representing medullosalean and marattialean tree-fern species, from two Carboniferous coalfields in Nova Scotia, Canada, are investigated. The samples were analyzed by infrared spectroscopy (FTIR), and by pyrolysis-gas chromatograph/mass spectrometry (py-Gc/Ms) techniques in search for chemical signatures that would help in developing a chemotaxonomic classification of Carboniferous fern species, assuming genetically dependent make-up of cuticles. FTIR-derived CH2/CH3 ratios, in conjunction with contributions from carboxyl groups, demonstrated a better potential for discriminating between medullosalean genera and species than molecular signatures obtained by py-Gc/Ms. However, the latter provided better data for differentiating medullosalean from marattialean tree ferns as a group. Changes in the chemical make-up of naturally macerated cuticles due to sample preparation are discussed. ?? 2001 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗
USGS1984

Interlaboratory comparison of mineral constituents in a sample from the Herrin (No. 6) coal bed from Illinois

Approximately 20 kg of the Herrin (No. 6) coal was collected from a strip mine in St. Clair County, Ill. A 10-kg portion was ground to -60 mesh, homogenized, and riffled into 128 splits of 70-80 g each. Homogeneity of these splits was confirmed by moisture, ash, and sulfur analyses of six randomly selected splits. Results of these analyses were within the ASTM (American Society for Testing and Materials) guidelines for interlaboratory precision. Splits of the Herrin (No. 6) coal were then transmitted to more than 30 laboratories for analysis. Low-temperature plasma oxidation was used to isolate inorganic matter for quantitative chemical and mineralogical analysis. Despite a wide variation in ashing conditions, only minor variations in ash yields were obtained; these variations were attributed to differences in operating temperature and moisture content. Mineralogical analyses of low-temperature ash (LTA) concentrates prepared by five different laboratories indicated variations within the limits of analytical error. The mean values, in weight percent, for the major minerals are as follows: calcite, 9; quartz, 20; pyrite, 23; kaolinite, 14; and illite+mixed-layer clays, 31. Normative mineralogical calculations and Fourier transform infrared analysis (FTIR) yielded results similar to those obtained from X-ray diffraction (XRD). Choosing appropriate mineral standards was found to be critical for the proper use of analytical techniques such as XRD and FTIR. Good interlaboratory agreement was obtained for most major, minor, and trace elements despite differences in analytical procedures and in the type of sample analyzed (coal, high-temperature ash, or LTA). Discrepancies between analyses for zinc, strontium, manganese, and iron may be attributed to sampling inhomogeneity problems. Mossbauer spectroscopy showed that approximately 44 percent of the pyritic sulfur was lost through weathering in the first year after preparation of the interlaboratory sample. Szomolnokite and possibly coquimbite and jarosite were also identified. Scanning electron microscopy studies indicated ubiquitous pyrite framboids and, less commonly, euhedral crystals, skeletal grains, irregularly shaped particles, and vein fillings. Minor accessory minerals such as rare-earth phosphates and possibly silicates, zircon, barium sulfate, titanium oxide, and sphalerite were also found. The textural evidence indicates that the minerals in the banded material are detrital whereas the minerals occurring as vein and pore fillings are authigenic. Magnetic measurements indicate that coal crushed in a steel pulverizer is contaminated by small quantities of abrasion fragments from the crusher, which seriously affect the measured magnetic properties of the coal.

Circular↗
USGS2015

Mapping of coal quality using stochastic simulation and isometric logratio transformation with an application to a Texas lignite

Coal is a chemically complex commodity that often contains most of the natural elements in the periodic table. Coal constituents are conventionally grouped into four components (proximate analysis): fixed carbon, ash, inherent moisture, and volatile matter. These four parts, customarily measured as weight losses and expressed as percentages, share all properties and statistical challenges of compositional data. Consequently, adequate modeling should be done in terms of a logratio transformation, a requirement that is commonly overlooked by modelers. The transformation of choice is the isometric logratio transformation because of its geometrical and statistical advantages. The modeling is done through a series of realizations prepared by applying sequential simulation for the purpose of displaying the parts in maps incorporating uncertainty. The approach makes realistic assumptions and the results honor the data and basic considerations, such as percentages between 0 and 100, all four parts adding to 100% at any location in the study area, and a style of spatial fluctuation in the realizations equal to that of the data. The realizations are used to prepare different results, including probability distributions across a deposit, E-type maps displaying average properties, and probability maps summarizing joint fluctuations of several parts. Application of these maps to a lignite bed clearly delineates the deposit boundary, reveals a channel cutting across, and shows that the most favorable coal quality is to the north and deteriorates toward the southeast.

International Journal of Coal Geology↗
USGS1977

National coal resource investigations of the United States Geological Survey

The objective of this report is to provide a record of some of the goals and accomplishments of the coal resource investigations of the U. S. Geological Survey for 1977. Successful completion of these goals will aid the Nation in the years ahead because proper usage of coal resource data may lessen economic displacements resulting from the energy shortage. This report is concerned only with one mineral fuel -- coal -- and only with coal resource investigations in the Geologic Division of the U. S. Geological Survey. Other divisions involved with coal or coal-related work are the Conservation, Water Resources, and Topographic Divisions. It is one of a series of reports on the energy resource studies conducted by the Geological Survey that provide a public record of the objectives, activities, and accomplishments of these programs. Similar reports have been prepared on oil and gas, oil shale, uranium, thorium, and energy-related industrial minerals. This report includes descriptions of the program, each sub-element of the program, individual projects, and a selected list of program publications from 1970-76. It also describes how the program is responsive to Presidential pronouncements and Congressional mandates. The program is cooperative with several Federal bureaus, many state agencies, universities, and industry. This coordination assures that the program supplements the work of these interested groups and is not duplicative. A scientific program such as the coal resource investigations is difficult for the non-involved person to understand solely from the existing reports on various studies made in the program. This report provides an explanation that the scientist, decision maker, personnel of other government agencies, and the layman can use to relate various activities and to gain a better understanding of the relation of coal to the Nation's requirements for energy and of the importance of a carefully planned program on this energy resource.

Open-File Report↗
USGS2000

Stanford-USGS shrimp-RG ion microprobe: A new approach to determining the distribution of trace elements in coal

The distribution of Cr and other trace metals of environmental interest in a range of widely used U.S. coals was investigated using the Stanford-USGS SHRIMP-RG ion microprobe . Using the oxygen ion source, concentrations of Cr (11 to 176 ppm), V (23 to 248 ppm), Mn (2 to 149 ppm), Ni (2 to 30 ppm), and 13 other elements were determined in illite/smectite, a group of clay minerals commonly present in coal. The results confirm previous indirect or semi-quantitative determinations indicating illite/smectite to be an important host of these metals. Calibration was achieved using doped aluminosilicate-glass synthetic standards and glasses prepared from USGS rock standards. Grains for analysis were identified optically, and confirmed by 1) precursory electron microprobe analysis and wavelength-dispersive compositional mapping, and 2) SHRIMP-RG major element data obtained concurrently with trace element results. Follow-up investigations will focus on the distribution of As and other elements that are more effectively ionized with the cesium primary beam currently being tested.

ACS Division of Fuel Chemistry, Preprints↗
USGS1979

Spatial variation in total element concentration in soil within the Northern Great Plains coal region and Regional soil chemistry in Bighorn and Wind River basins, Wyoming and Montana

PART A: To objectively determine the changes in chemical character of an area subjected to mining and reclamation, prior information is needed. This study represents a broadscale inventory of total chemical composition of the surficial materials of the Northern Great Plains coal region (western North and South Dakota, eastern Montana, and northeastern Wyoming); data are given for 41 elements in A and C soil horizons. An unbalanced, nested, analysis-of-variance design was used to quantify variation in total content of elements between glaciated and unglaciated terrains, for four increasingly smaller geographic scales, and to quantify variation due to sample preparation and analysis. From this statistical study, reliable maps on a regional basis (>100 km) were prepared for C, K, and Rb in A and C soil horizons; for N a, Si, Th, D, and Zn in A-horizon soil; and for As, Ca, Ge, and Mg in C-horizon soil. The distribution of variance components for the remaining 29 elements did not permit the construction of reliable maps. Therefore, a baseline value for each of these elements is given as a measure of the total element concentration in the soils of the Northern Great Plains coal region. The baseline is expressed as the 95-percent range in concentration to be expected in samples of natural soils. PART B: A reconnaissance study of total concentrations of 38 elements in samples of soils (0-40 cm deep, composite) from the Bighorn and Wind River Basins of Montana and Wyoming indicates that the geographic variation for most elements occurs locally (5 km or less). However, in the Bighorn Basin, Zn exhibits significant regional variation (between geologic units); and in the Wind River Basin, AI, Cr, K, Mn, Mo, Ni, U, and V exhibit similar variation. For the remaining elements, the lack of regional variation suggests that a single summary statistic can be used to estimate a baseline value that reflects the range in concentration to be expected in samples of soils in each basin. The concentrations of most of these elements in both basins are not much different from those measured independently in the Powder River Basin of Wyoming or in the Western United States. In addition, data from an analysis of variance provide an estimate of the number of random samples within an area of specified size (10 km square, approximately a township) that are needed to prepare a reliable map of total element concentration in soils for each of the elements in each of the basins.

Montana, North Dakota, Saskatchewan, South Dakota,↗
USGS2010

Factors Affecting Specific-Capacity Tests and their Application--A Study of Six Low-Yielding Wells in Fractured-Bedrock Aquifers in Pennsylvania

This report by the U.S. Geological Survey, prepared in cooperation with the Pennsylvania Department of Environmental Protection, Bureau of Mining and Reclamation, evaluates factors affecting the application of specific-capacity tests in six low-yielding water wells in areas of coal mining or quarrying in Pennsylvania. Factors such as pumping rate, duration of pumping, aquifer properties, wellbore storage, and turbulent flow were assessed by theoretical analysis and by completing multiple well tests, selected to be representative of low-yielding household-supply wells in areas of active coal mining or quarrying. All six wells were completed in fractured-bedrock aquifers--five in coal-bearing shale, siltstone, sandstone, limestone, and coal of Pennsylvanian and Permian age and one in limestone of Cambrian age. The wells were pumped 24 times during 2007-09 at rates from 0.57 to 14 gallons per minute during tests lasting from 22 to 240 minutes. Geophysical logging and video surveys also were completed to determine the depth, casing length, and location of water-yielding zones in each of the test wells, and seasonal water-level changes were measured during 2007-09 by continuous monitoring at each well. The tests indicated that specific-capacity values were reproducible within about ? 20 percent if the tests were completed at the same pumping rate and duration. A change in pumping duration, pumping rate, or saturated aquifer thickness can have a substantial effect on the comparability of repeated tests. The largest effect was caused by a change in aquifer thickness in well YO 1222 causing specific capacity from repeated tests to vary by a factor of about 50. An increase in the duration of pumping from 60 to 180 minutes caused as much as a 62 percent decrease in specific capacity. The effect of differing pumping rates on specific capacity depends on whether or not the larger rate causes the water level in the well to fall below a major water-yielding zone; when this decline happened at well CA 462, specific capacity was reduced by about 63 percent. Estimates of the maximum yield for low-yielding wells that are computed by multiplying the available drawdown by the specific-capacity value may contain large errors if the wells were pumped at low rates that do not cause much water-level drawdown. The estimates of yield are likely to be too large because the effects of lowering the water level in the well below water-yielding zones have not been incorporated. Better yield estimates can be made by the use of step-drawdown tests or by over-pumping at a rate large enough to dewater most of the wellbore. The maximum well yield, after overpumping, can be estimated from the rate of water-level recovery or by subtracting the incremental rate of change of borehole storage at the end of the test from the pumping rate.

Pennsylvania↗
USGS1999

Hydrologic assessment of the Upper Dorr Run Watershed, Hocking County, Ohio, 1998

The Upper Dorr Run Watershed in Hocking County, Ohio, has been mined several times for coal and clay since 1913 and is a significant source of acid mine drainage to the Hocking River. To assess the surface-water hydrology of the site, a topographic map showing the location of springs and other hydrologic features of interest was prepared using aerial photography and field surveying and mapping techniques. Discharge and water-quality measurements at six springs and one stream site were made during field investigations in June 1998. Discharge and water quality observed at a downstream weir on Upper Dorr Run represents the combined discharge from springs plus ground-water inflow. Discharges from springs to surface water were generally small (less than 0.3 cubic foot per second), but one spring constituted 56 percent of the total discharge measured at the downstream weir. The total flow at an intermediate measurement site was less than the combined discharge of the upgradient springs because of evaporation, transpiration, and ground-water flow beneath the stream channel. The total flow at the weir was greater than the combined discharge of all springs, primarily because two potential sources of water were not included in field measurements. The water quality in Upper Dorr Run is strongly affected by acid mine drainage as indicated by pH less than 4, elevated acidity, and elevated concentrations of dissolved sulfate and dissolved iron. Concentrations of chemical constituents in the water were lower at the downstream weir than at the source springs because of residence times in ponds and chemical interactions between the water and the atmosphere. Acidity loads during the sampling period were significantly higher from the Lower Kittanning (No. 5) coal (272 kilograms per day) than from the Upper Kittanning (No. 6) coal (17.7 kilograms per day). Comparison of data obtained in 1998 to data obtained in 1982 showed that quality of water of selected sampling sites had not changed appreciably in 16 years.

Water-Resources Investigations Report↗