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At least 19 recordsLinked to original sources

Geochemistry and petrology of selected coal samples from Sumatra, Kalimantan, Sulawesi, and Papua, Indonesia

Indonesia has become the world's largest exporter of thermal coal and is a major supplier to the Asian coal market, particularly as the People's Republic of China is now (2007) and perhaps may remain a net importer of coal. Indonesia has had a long history of coal production, mainly in Sumatra and Kalimantan, but only in the last two decades have government and commercial forces resulted in a remarkable coal boom. A recent assessment of Indonesian coal-bed methane (CBM) potential has motivated active CBM exploration. Most of the coal is Paleogene and Neogene, low to moderate rank and has low ash yield and sulfur (generally < 10 and < 1??wt.%, respectively). Active tectonic and igneous activity has resulted in significant rank increase in some coal basins. Eight coal samples are described that represent the major export and/or resource potential of Sumatra, Kalimantan, Sulawesi, and Papua. Detailed geochemistry, including proximate and ultimate analysis, sulfur forms, and major, minor, and trace element determinations are presented. Organic petrology and vitrinite reflectance data reflect various precursor flora assemblages and rank variations, including sample composites from active igneous and tectonic areas. A comparison of Hazardous Air Pollutants (HAPs) elements abundance with world and US averages show that the Indonesian coals have low combustion pollution potential.

International Journal of Coal Geology↗

Review and update of the applications of organic petrology: Part 1, geological applications

Organic petrology developed as coal petrology at the beginning of the 20th century dedicated mainly to the study of coals because of their utilization in industry. Coal petrology was then considered a branch of coal science. Later, with the development of specialized nomenclature, classification of coal components, and the standardization and improvement of analytical (microscopical) methods, this discipline expanded in interests and name, becoming organic petrology. Organic petrology carries a broader context, being as well a tool applied in the study of dispersed organic matter in sedimentary rocks due to its importance in exploration for fossil fuel resources. At present, organic petrology is a discipline widely recognized for its role in fundamental and applied research with respect to both coal utilization and in geosciences. Throughout the 20th century several important monographs have been published on the discipline of organic petrology, including “Stach's textbook of coal petrology” (1st edition 1935, 2nd 1975, 3rd 1982), updated as the more general “Organic petrology” by Taylor et al. (1998). More recently, the text “Applied coal petrology: the role of petrology in coal utilization” was published by Suárez-Ruiz and Crelling (2008). This review is the first in a two-part review series that describes and updates the role of organic petrology in geosciences. A second part complementing this one and focused on the applications of organic petrology to other scientific fields will follow.

International Journal of Coal Geology↗

The petrology of dispersed organic matter in sedimentary rocks: Review and update

Organic petrology developed from coal petrology, and, in the 1960s, it began to be applied to the study of dispersed organic matter (DOM) in sedimentary rocks other than coal. Over the last few decades, the petrology of DOM has been used to characterize organic matter in sedimentary basins with an emphasis on fossil fuel resource exploration. Today, due to the global research shift on topics related to climate, organic petrology has expanded into new application areas, such as geothermal exploration, biological carbon storage (biochar), disposal, and management of radioactive waste. From the publication of the International Handbook of Coal Petrology (mid-20th century) to the present day, a large number of standards, books, and articles have been published as a result of the work of organic petrographers and petrologists around the world and efforts of the International Committee for Coal and Organic Petrology (ICCP) and The Society for Organic Petrology (TSOP) to promote the study of organic petrology. The current fundamentals and standards of organic petrology provide the international scientific community with well-informed guidance and recommendations to promote in-depth research. However, this information is currently widely scattered, leading to discrepancies in methodology and terminology. Therefore, this paper aims to present a comprehensive review of the main analytical standard test methods and techniques currently used in the petrology of DOM under reflected white light and UV and blue-light excitation, and to provide an efficient and well-defined reference guide. Furthermore, considering the important role of the ICCP in the development of organic petrology since the 1950s, a brief review of the ongoing activities of ICCP dealing with DOM is also presented.

International Journal of Coal Geology↗

Identifying the effects of petrologic processes in a closed basaltic system using trace element concentrations in olivines and glasses: Implications for comparative planetology

We use trace-element concentrations in olivines and glasses from a closed basaltic system to identify the effects of petrologic processes on the trace-element record of that system. The closed basaltic system in question is the Makaopuhi Lava Lake (MLL), which is closed with respect to magma mixing. Detailed studies of this lava lake have provided important information about system variables and petrologic processes that have been measured and observed at the lake. These previous studies show that olivine crystallized from the lava lake at all stages of the lake’s evolution, which means that olivine and residual glasses contain a record of the lake’s petrologic history. We use this information, in conjunction with variations in trace-element concentrations in olivines and glasses, to show that mineral crystallization, gravitational settling, convective flow, filter pressing, and mineral-melt interface kinetics have characteristic effects on the trace element record of a closed basaltic system. These results are pertinent to the field of comparative planetology because they can be used to evaluate petrologic information in small samples from other planetary bodies, where information about system variables and/or petrologic processes is limited.

Hawaii↗

Petrologic testament to changes in shallow magma storage and transport during 30+ years of recharge and eruption at Kīlauea Volcano, Hawai‘i

Petrologic monitoring of Kīlauea Volcano from January 1983 to October 2013 has yielded an extensive record of glass, phenocryst, melt inclusion, and bulk-lava chemistry from well-quenched lava. When correlated with 30+ years of geophysical and geologic monitoring, petrologic details testify to physical maturation of summit-to-rift magma plumbing associated with sporadic intrusion and prolonged magmatic overpressurization. Changes through time in bulk-lava major- and trace-element compositions, along with glass thermometry, record shifts in the dynamic balance of fractionation, mixing, and assimilation processes inherent to magma storage and transport during near-continuous recharge and eruption. Phenocryst composition, morphology, and texture, along with the sulfur content of melt inclusions, constrain coupled changes in eruption behavior and geochemistry to processes occurring in the shallow magmatic system. For the first 17 years of eruption, magma was steadily tapped from a summit reservoir at 1–4 km depth and circulating between 1180 and 1200°C. Furthermore, magma cooled another 30°C while flowing through the 18 km long rift conduit, before erupting olivine-spinel-phyric lava at temperatures of 1150–1170°C in a pattern linked with edifice deformation, vent formation, eruptive vigor, and presumably the flux of magma into and out of the summit reservoir. During 2000–2001, a fundamental change in steady state eruption petrology to that of relatively low-temperature, low-MgO, olivine(-spinel)-clinopyroxene-plagioclase-phryic lava points to a physical transformation of the shallow volcano plumbing uprift of the vent. Preeruptive comagmatic mixing between hotter and cooler magma is documented by resorption, overgrowth, and compositional zonation in a mixed population of phenocrysts grown at higher and lower temperatures. Large variations of sulfur (50 to >1000 ppm) in melt inclusions within individual phenocrysts and among phenocrysts in most samples provide an unequivocal glimpse of rapid crystal growth amid sulfur degassing at <30 MPa in a turbulent preeruptive environment. We speculate that, during the last decade, one or more shallow open-system reservoirs developed along the conduit between the summit and Pu‘u ‘Ō‘ō and now serve to buffer the magmatic throughput associated with ongoing recharge and eruption. Lava with identical trace-element signatures erupted simultaneously at the summit and at Pu‘u ‘Ō‘ō from 2008 to 2013 confirms magmatic continuity between the vents. Complementary changes in compositions of matrix glasses, phenocrysts, and melt inclusions of summit tephra are mirrored by similar changes in contemporaneous rift lava at eruption temperatures 20–35°C lower than those at the summit. Petrologic parameters measured at opposite ends of the shallow magmatic plumbing system are both correlated with summit deformation, demonstrating that effects of summit magma chamber pressurization are translated throughout interconnected magma pathways in the shallow edifice.

Hawaii↗

Proceedings of the twentieth annual meeting of the Society for Organic Petrology

The Society for Organic Petrology (TSOP; pronounced "Tee'-sop") was established in 1984 to consolidate and foster the organizational activities of scientists and engineers involved with coal petrology, kerogen petrology, organic geochemistry, and related disciplines. The following report, "Proceedings of the Twentieth Annual Meeting of The Society for Organic Petrology" (ISSN 1060-7250), features technical talks, poster presentations, business meetings, short courses, and field trips from the Fall 2003 annual meeting held in Washington, D.C.

Open-File Report↗

Summary of the research work of the Trace Elements Section, Geochemistry and Petrology Branch, for the period April 1, 1948-December 31, 1950

This report summarizes the research work of the Trace Elements Section, Geochemistry and Petrology Branch, from the organization of the Section in April 1948 to December 31, 1950. The research undertaken thus far consists of laboratory and related field studies in the following fields: 1. Mineralogic and petrologic investigations of radioactive rocks, minerals, and ores. 2. Investigations of chemical methods of analysis for uranium, thorium, and other elements and compounds in radioactive materials, and related chemical problems. 3. Investigations of spectrographic methods of analysis for a wide variety of elements in radioactive materials. 4. Investigations of radiometric methods of analysis as applied to radioactive materials. It should be emphasized that the work undertaken thus far, described under the headings "Future work", is almost entirely in the nature of investigations supporting the field appraisal of known important uraniferous deposits. A comprehensive program of more fundamental research was submitted in April 1949 in a report entitled "Proposed program of desirable research in the geochemistry of uranium," but funds for this work have not been authorized. It is hoped, however, that funds to support basic research of the type indicated in that report may be available in the future. This report does not cover the analytical work of the Section nor the public-sample program. The analytical work has been summarized for the fiscal year 1950 in the report, "Numerical summary of the analytical work of the Trace Elements Section, Geochemistry and Petrology Branch, for the fiscal year 1950," by John C. Rabbit, U.S. Geol. Survey Trace Elements Memorandum Rept. 174, October 1950. A report on the public-sample program is in preparation. Much of the material in this report has been paraphrased from reports prepared by members of the Section. My special thanks are due them; to Earl Ingerson, chief of the Geochemistry and Petrology Branch of the Survey, for his critical review; to my secretary, Marie Woolihan, for her aid in collecting material; and to Virginia Layne of the editorial staff of the Section for typing the manuscript and the multilith mats.

Trace Elements Investigations↗

Summary of the research work of the Trace Elements Section, Geochemistry and Petrology Branch, for the period January 1-March 31, 1951

This report summarized the research work of the Trace Elements Section, Geochemistry and Petrology Branch for the period January 1 - March 31, 1951. Work before that is summarized in an earlier report, "Summary of the research work of the Trace Elements Section, Geochemistry and Petrology Branch, for the period April 1, 1948 - December 31, 1950," by John C. Rabbitt (U.S. Geol. Survey Trace Elements Investigations Rept. 148, January 1951). This report will be referred to as TEIR 148. In TEIR 148 the purpose of each project was described and it is not thought necessary to repeat that material. The research work of the section consists of laboratory and related field studies in the following fields: 1. Mineralogic and petrologic investigations of radioactive rocks, minerals, and ores. 2. Investigations of chemical methods of analysis for uranium, thorium, and other elements and compounds in radioactive materials, and related chemical problems. 3. Investigations of spectographic method of analysis for a wide variety of elements in radioactive materials. 4. Investigation of radiometric methods of analysis is applied to radioactive materials. It should be emphasized that the work undertaken so far is almost entirely in the nature of investigations supporting the field appraisal of known uraniferous deposits. A program of more fundamental research, particularly in the mineralogy and geochemistry of uranium, is now being drawn up and will be submitted for approval soon. This report does not deal with the routine analytical work of the Section nor the public-sample program. The analytical work will be summarized in a report to be issued after the end of fiscal year 1951, and a report on the public-sample program is in process. Special thanks are due members of the Section who are engaged in the research work and who have supplied material for this report, the Early Ingerson, Chief of the Geochemistry and Petrology Branch for his critical review, to Jane Titcomb of the editorial staff of the Section for editing the report, and to Virginia Layne of the same staff, for typing the manuscript and the multilith mats.

Trace Elements Investigations↗

Review and update of the applications of organic petrology: Part 2, geological and multidisciplinary applications

The present paper is focused on organic petrology applied to unconventional and multidisciplinary investigations and is the second part of a two part review that describes the geological applications and uses of this branch of earth sciences. Therefore, this paper reviews the use of organic petrology in investigations of: (i) ore genesis when organic matter occurs associated with mineralization; (ii) the behavior of organic matter in coal fires (self-heating and self-combustion); (iii) environmental and anthropogenic impacts associated with the management and industrial utilization of coal; (iv) archeology and the nature and geographical provenance of objects of organic nature such as jet, amber, other artifacts and coal from archeological sites; and (v) forensic science connected with criminal behavior or disasters. This second part of the review outlines the most recent research and applications of organic petrology in those fields.

International Journal of Coal Geology↗

Petrology of Newberry Volcano, central Oregon

Note: This paper is dedicated to Aaron and Elizabeth Waters on the occasion of Dr. Waters' retirement. The eastern flank of the central and southern Cascade Mountains is bordered by a belt of shield volcanoes that appears to be a subprovince of the Oregon high-alumina plateau basalt petrologic province. Most of the volcanoes in this belt are low shields in which differentiation from the parent high-alumina basalt magma has been relatively slight, but several are large complex shield centers where differentiation has been extreme. The location of these large centers, and of some of the smaller volcanoes as well, was largely determined by intersecting concentrations of faults and fault-fissures of three regional fault systems. One of the largest of the complex volcanic centers is Newberry Volcano in central Oregon, a shield volcano with a big caldera at its summit. The stratigraphy of the caldera walls and of features on the caldera floor at Newberry allows detailed interpretation of the history of the younger parts of the volcano and caldera. The formation of Newberry Caldera was apparently a slow process controlled largely by faulting along the three regional fault systems. The magma conduits were probably a gridlike plexus of intersecting dikes and fissures, with larger “magma pockets” at the grid intersections. The magma was trapped in shallow chambers and periodically released by faulting. The entrapment of the magma allowed differentiation in the shallow chambers. The stratigraphy and petrology of the wall sequence also allows determination of the relative time at which the caldera had grown large enough to hold a caldera lake. On differentiation plots, chemical analyses of the Newberry rocks show two trends: rocks erupted before the presence of a lake in the caldera trend toward slight iron enrichment, whereas rocks erupted after water was present in the caldera generally trend toward alkali enrichment. These different trends are attributed to differences in the oxygen fugacity of the magma which, in turn, are related to the presence or absence of large volumes of water in the caldera lake. The interpretation is supported by field, petrographic, petrologic, chemical, trace-element, and isotopic data. Plots of existing data for the Medicine Lake Highland Volcano, another large complex shield center in the belt, show the same type of two-trend relation as those of Newberry Volcano.

Oregon↗

Application of organic petrology in high maturity shale gas systems

Application of incident light microscopy techniques for organic petrology in high temperature thermogenic shale gas systems demonstrates that solid bitumen is the dominant organic matter. Solid bitumen is retained as a residual conversion product as oil-prone kerogen cracks to hydrocarbons or occurs from the cracking of once liquid oil. Oil-prone Type I/II kerogens are not present in shale gas reservoirs, already having converted to hydrocarbons. Type III/IV kerogens (vitrinite and inertinite) are refractory and persist in shale gas reservoirs to high maturity with little morphological change apart from condensation and aromatization causing higher reflectance. Organic petrology applications are most useful for thermal maturity determination and delineation of hydrocarbon windows through measurement of vitrinite reflectance and vitrinite reflectance equivalents from other organic matter (zooclasts and/or solid bitumen). Depositional organo-facies determination generally is not possible in the gas window of thermal maturity; fluorescence microscopy is not useful as organic matter is no longer autofluorescent. Application of scanning electron microscopy (SEM) allows observation of an interconnected nano-scale organic porosity in shale gas systems but suffers from inability to identify organic matter types. SEM approaches to shale gas reservoir characterization therefore should not attempt differentiation of kerogen types or kerogen vs. solid bitumen identification unless correlative organic microscopy is performed. Herein are reviewed organic petrology results as used in the shale gas systems of North America, Europe and China, including SEM applications, citing recent examples from the literature.

Book chapter↗

Petrologic and isotopic data from the Cretaceous (Campanian) Blackhawk Formation and Star Point Sandstone (Mesaverde Group), Wasatch Plateau, Utah

The presence of discrete minerals associated with coal—whether (1) detrital or authigenic constituents of the coals or in thin mudstone or siltstone units interbedded with coals, or (2) authigenic phases that formed along cleats—might influence its utilization as an energy resource. The build-up of sintered ash deposits on the surfaces of heat exchangers in coal-fired power plants, due to the alteration of minerals during combustion of the coal, can seriously affect the functioning of the boiler and enhance corrosion of combustion equipment. In particular, the presence of sodium in coals has been considered a key factor in the fouling of boilers; however, other elements (such as calcium or magnesium) and the amount of discrete minerals burned with coal can also play a significant role in the inefficiency of and damage to boilers. Previous studies of the quality of coals in the Cretaceous (Campanian) Blackhawk Formation of the Wasatch Plateau, Utah, revealed that the sodium content of the coals varied across the region. To better understand the origin and distribution of sodium in these coals, petrologic studies were undertaken within a sedimentological framework to evaluate the timing and geochemical constraints on the emplacement of sodium-bearing minerals, particularly analcime, which previously had been identified in coals in the Blackhawk Formation. Further, the study was broadened to include not just coals in the Blackhawk Formation from various localities across the Wasatch Plateau, but also sandstones interbedded with the coals as well as sandstones in the underlying Star Point Sandstone. The alteration history of the sandstones in both formations was considered a key component of this study because it records the nature and timing of fluids passing through them and the associated precipitation of sodium-bearing minerals; thus, the alteration history could place constraints on the distribution and timing of sodium mineralization in the interbedded or overlying Blackhawk coals. Although some preliminary results were previously presented at scientific meetings, the petrologic and geochemical data have not been fully compiled and reported. The purpose of this report is to present the methods of data acquisition and the results of petrologic and isotopic analyses on coal and sandstone samples from the Blackhawk Formation as well as sandstones of the underlying Star Point Sandstone.

Utah↗

Petrologic insights into basaltic volcanism at historically active Hawaiian volcanoes

Study of the petrology of Hawaiian volcanoes, in particular the historically active volcanoes on the Island of Hawai&lsquo;i, has long been of worldwide scientific interest. When Dr. Thomas A. Jaggar, Jr., established the Hawaiian Volcano Observatory (HVO) in 1912, detailed observations on basaltic activity at Kīlauea and Mauna Loa volcanoes increased dramatically. The period from 1912 to 1958 saw a gradual increase in the collection and analysis of samples from the historical eruptions of Kīlauea and Mauna Loa and development of the concepts needed to evaluate them. In a classic 1955 paper, Howard Powers introduced the concepts of magnesia variation diagrams, to display basaltic compositions, and olivine-control lines, to distinguish between possibly comagmatic and clearly distinct basaltic lineages. In particular, he and others recognized that Kīlauea and Mauna Loa basalts must have different sources. Subsequent years saw a great increase in petrologic data, as the development of the electron microprobe made it possible to routinely monitor glass and mineral compositions, in addition to bulk rock compositions. We now have 100 years&rsquo; worth of glass compositions for Kīlauea summit eruptions, which, together with expanding databases on prehistoric tephras, provide important constraints on the nature of Kīlauea&rsquo;s summit reservoir. A series of chemically distinctive eruptions in the 1950s and 1960s facilitated evaluation of magma mixing and transport processes at Kīlauea. At Mauna Loa, lava compositions are distinctive only at the trace element level, suggesting that its summit reservoir is better mixed than Kīlauea&rsquo;s. Most summit lavas at both volcanoes, however, lie on olivine control lines having the same olivine composition (Fo 86&ndash;87 ). Study of the ongoing East Rift Zone eruption at Kīlauea has further illuminated the complexity of magma storage, resupply, and mixing along this very active rift zone. Studies of active and closed-system lava lakes have been part of HVO&rsquo;s efforts since Jaggar&rsquo;s unique descriptions of the Halema&lsquo;uma&lsquo;u lava lake that existed before 1924. Detailed study of closed-system bodies, including the 1959 Kīlauea Iki, 1963 &lsquo;Alae, and 1965 and prehistoric Makaopuhi lava lakes and the Uēkahuna laccolith, have allowed recognition and quantification of processes of basalt differentiation. Specific topics reviewed herein include the occurrence of segregation veins and related structures, overall cooling history, and patterns of crystallization and reequilibration of olivine in various lava lakes. In recent decades, study of the submarine slopes of the Island of Hawai&lsquo;i and of Lō&lsquo;ihi Seamount has revolutionized our understanding of the early history of Hawaiian volcanoes. Observations of Lō&lsquo;ihi lavas first established the existence of an early alkalic stage in the evolution of Hawaiian volcanoes. Stages of volcanic development from inception to tholeiitic shield building can be observed in Kīlauea&rsquo;s submarine and subaerial sections. One distinctive feature of submarine volcanics at Kīlauea, Mauna Loa, and Hualālai is that picritic lavas are more abundant than in subaerial eruptions. Also, olivine compositions of submarine lavas are more magnesian, ranging from Fo 88 at Kīlauea to Fo 89 at Hualālai. The most magnesian glasses known from Kīlauea (MgO=14.7&ndash;15.0 weight percent) were found along the submarine part of Kīlauea&rsquo;s East Rift Zone. Contributions to our knowledge of the nature of the mantle source(s) of Hawaiian basalts are reviewed briefly, although this is a topic where debate is ongoing. Finally, our accumulated petrologic observations impose constraints on the nature of the summit reservoirs at Kīlauea and Mauna Loa, specifically whether the summit chamber has been continuous or segmented during past decades.

Hawaii↗

Interactive computer programs for petrologic modeling with extended Q-mode factor analysis

An extended form of Q-mode factor analysis may be used if the row-sums of the data matrix are constant and can be helpful especially in developing and testing petrologic-mixing models for igneous systems. The first step is to represent the sample compositions as unit vectors in M-dimensional space and then to project them into space of fewer dimensions (m) as determined to be appropriate from a factor-variance diagram. Compositions thought to be those of possible end-members in the petrologic system then are represented as vectors in the M-dimensional space and projected into the same space as the sample vectors. If these vectors remain close to unity in length after projection, the corresponding compositions can serve as end-member compositions for the model. After m suitable end-member compositions have been identified, each sample composition is expressed as a mixture of the end-members by computation of the composition loadings. The interactive computer programs presented are useful in these procedures because of the trial-and-error nature of the modeling procedures. ?? 1976.

Computers & Geosciences↗

PETRO.CALC.PLOT, Microsoft Excel macros to aid petrologic interpretation

PETRO.CALC.PLOT is a package of macros which normalizes whole-rock oxide data to 100%, calculates the cation percentages and molecular proportions used for normative mineral calculations, computes the apices for ternary diagrams, determines sums and ratios of specific elements of petrologic interest, and plots 33 X-Y graphs and five ternary diagrams. PETRO.CALC.PLOT also may be used to create other diagrams as desired by the user. The macros run in Microsoft Excel 3.0 and 4.0 for Macintosh computers and in Microsoft Excel 3.0 and 4.0 for Windows. Macros provided in PETRO.CALC.PLOT minimize repetition and time required to recalculate and plot whole-rock oxide data for petrologic analysis. ?? 1994.

Computers & Geosciences↗

Lateral variation in geochemistry, petrology, and palynology in the Elswick coal bed, Pike County, Kentucky

The Middle Pennsylvanian/Langsettian (Westphalian A) Elswick coal bed, correlative to the Upper Banner of Virginia, is a rare example of a mined high-sulfur (> 2%) coal in Eastern Kentucky, a region known for low-sulfur coals. To characterize lateral variation in the geochemistry, petrography, and palynology of the Elswick coal bed, three sites were sampled along a southeast-northwest transect within a single mine. At the southeastern site, the lower 101??cm of the 116-cm thick coal is dull, generally dominated by durain and dull clarain. While all benches at this site fit within the previously-defined "mixed palynoflora - moderate/low vitrinite group," suggesting a stressed environment of deposition, the palynology of the benches of the dull interval show greater diversity than might be expected just from the petrology. Lithology is generally similar between the sites, but each site has some differences in the petrology. Overall, the coal bed shows significant lateral variation in properties at the mine scale, some of which can be attributed to the gain or loss of upper and lower lithologies, either through an actual physical merging or through the change in character of lithotypes. Sulfur content varies between the three sites examined for this study. Site 3, located in the northwestern portion of the study area is characterized by a strikingly high sulfur zone (7.45%) in the middle of the coal bed, a feature missing at the other sites. Pyrite and marcasite, in a mid-seam lithotype at the northwestern site (site 3), show signs of overgrowths, indicating multiple generations of sulfide emplacement. The high-sulfur site 3 lithologies all have massive overgrowths of euhedral and framboidal pyrite, fracture- and cleat-fill pyrite, and sulfide emplacement in fusinite lumens. Sulfur is high throughout the mine area, but variations are evident in the extent of secondary growth of sulfides. ?? 2006 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Development of web-based organic petrology photomicrograph atlases and internet resources for professionals and students

With advances in web applications, organic petrography and other related disciplines are in need of updated online resources and educational tools to aid professionals and students in the identification and interpretation of macerals. The U.S. Geological Survey (USGS) Organic Petrology Laboratory along with USGS Eastern Energy Resources Science Center Information Technology staff have developed five web atlases containing images of organic matter in geologic materials: 1. an American Society for Testing and Materials (ASTM) Atlas, 2. an Organic Petrology Taxonomy for International Classification (OPTIC) of Coal Macerals Atlas, 3. an Interactive Gulf Coast Photomicrograph Web Atlas (I-Map), 4. an Organic Material in Shales Atlas (Shale), and 5. an interactive Blue/White/Ultraviolet (UV) Light Atlas (Light). Each web atlas contains images of macerals with associated sample and petrographic data collected by the USGS. These webpages will provide means to preserve and circulate petrographic data collected by the USGS for coal and shale samples from all over the world.

International Journal of Coal Geology↗