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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↗

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↗

Q-mode factor analysis of compositional data

An extended form of the method of Q-mode factor analysis may be used if the rows of the data matrix sum to a constant. The constant row-sum provides a means for scaling the factor model to conform to the units of the original data in such forms as proportions, percentages, or parts per million. The scale factors for an m-factor model are used to derive composition scores and loadings, which lead to the same reproduced data regardless of the choice of reference axes (end-members). Factor-variance diagrams may be constructed to show the proportion of the variance that will be accounted for in each compositional variable by models containing various numbers of end-members. The method may be used to develop a petrologic mixing model by searching for end-members that are geologically plausible. ?? 1976.

Computers & Geosciences↗

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↗

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↗

Layered intrusions of the Duluth Complex, Minnesota, USA

The Duluth Complex and associated subvolcanic intrusions comprise a large (5,000 km 2 ) intrusive complex in northeastern Minnesota that was emplaced into comagmatic volcanics during the development of the 1.1 Ga Midcontinent rift in North America. In addition to anorthositic and felsic intrusions, the Duluth Complex is composed of many individual mafic layered intrusions of tholeiitic affinity. The cumulate stratigraphies and cryptic variations of six of the better exposed and better studied intrusions are described here to demonstrate the variability in their cumulus mineral paragenesis. Although the general paragenetic sequence is: O1(±Pl) → Pl+Ol → Pl+Cpx+Ox(±Ol±Opx) → Pl+Cpx+Ox+Ap(±Ol) considerable differences exist among the six intrusions in the relative order and timing of cumulus arrivals, most notably with regard to augite (Cpx) and Fe-Ti oxide (Ox). The various cumulate stratigraphies and cryptic variations represented by the six intrusions described here largely reflect differences in the degree of open-system behaviour to recharge, eruption, and country-rock assimilation, but also may have been influenced by differences in parent magma composition, in the efficiency of fractional crystallization, and in the conditions of crystallization ( e.g. P total , f O2 P H2O ). The Sonju Lake intrusion, wherein cumulus augite arrived before ilmenite, formed by essentially closed-system fractional crystallization. However, its compositional evolution may have been affected to an uncertain degree by assimilation of a granitic hanging-wall. The monotonous, thick troctolitic cumulate sequences of the lower parts of the South Kawishiwi and Partridge River Intrusions appear to represent the effects of frequent magma recharge coupled with in situ (or boundary layer) crystallization though other interpretations have been proposed. Extensive Cu-Ni sulphide mineralization at the base of these intrusions is attributed to country-rock contamination of the earliest intruded magmas. The cyclical progression of cumulates in the Layered Series at Duluth, wherein cumulus augite and oxide arrived nearly simultaneously, formed in a moderately open system characterized by periodic eruption and recharge. The Wilder Lake Intrusion is different from other intrusions in that cumulus ilmenite appears before augite and that olivine and augite composition define an inverted cryptic variation. The latter phenomenon may be related to a strong upward gradation toward lesser amounts of trapped liquid in the cumulates. Finally, the incomplete cumulate stratigraphy of the Bald Eagle Intrusion, which is composed of approximately equal thicknesses of troctolite (PO) and gabbro (PAO) adcumulates, is unique in that Fe-Ti oxide did not arrive as a cumulus phase despite prolonged crystallization of cumulus augite. These different cumulus parageneses probably produced a variety of derivative magmas, which may have contributed in part to the compositional diversity of the Midcontinent rift volcanics.

Developments in Petrology↗

Telescoping metamorphic isograds: Evidence from 40Ar/39A dating in the Orange-Milford belt, southern Connecticut

New 40 Ar/ 39 Ar ages for hornblende and muscovite from the Orange-Milford belt in southern Connecticut reflect cooling from Acadian amphibolite facies metamorphism between ∼380 to 360 Ma followed by retrograde recrystallization of fabric-forming muscovite and chlorite during lower greenschist facies Alleghanian transpression at ∼280 Ma. Reported field temperature and pressure gradients are improbably high for these rocks and a NW metamorphic field gradient climbing from chlorite-grade to staurolite-grade occurs over less than 5 km. Simple tilting cannot account for this compressed isograd spacing given the geothermal gradient of ∼20 °C/km present at the time of regional metamorphism. However, post-metamorphic transpression could effectively telescope the isograds by stretching the belt at an oblique angle to the isograd traces. Textures in the field and in thin section reveal several older prograde schistosities overprinted by lower greenschist facies fabrics. The late cleavages commonly occur at the scale of ∼100 μm and these samples contain multiple age populations of white mica. 40 Ar/ 39 Ar analysis of these poly-metamorphic samples with mixed muscovite populations yield climbing or U-shaped age spectra. The ages of the low temperature steps are late Paleozoic, while the ages of the older steps are late Devonian. These results support our petrologic interpretation that the younger cleavage developed under metamorphic conditions below the closure temperature for Ar diffusion in muscovite, that is, in the lower greenschist facies. The correlation of a younger regionally reproducible age population with a pervasive retrograde muscovite ± chlorite cleavage reveals an Alleghanian (∼280 Ma) overprint on the Acadian metamorphic gradient (∼380 Ma). Outcrop-scale structures including drag folds and imbricate boudins suggest that Alleghanian deformation and cleavage development occurred in response to dextral transpression along a northeast striking boundary. Alleghanian oblique collision of accreting terranes from the northeast would have resulted in northeast-southwest dextral transpression against the New York promontory. This deformation was responsible for crystallization of pervasive retrograde muscovite + chlorite cleavages and associated telescoping of the Acadian metamorphic isograds in southern Connecticut at ∼280 Ma.

Connecticut↗

Volcanic history of the San Juan Mountains, Colorado, as indicated by potassium-argon dating

Volcanic rocks in the San Juan Mountains constitute the largest erosional remnant of a once nearly continuous volcanic field that extended over much of the southern Rocky Mountains and adjacent areas in Oligocene and later time. Recent regional studies have shown that the gross petrologic evolution throughout the San Juan remnant of this field was relatively simple, with initial intermediate lavas and breccias, followed closely in time by more silicic ash-flow tuffs, and ending with a bimodal association of basalt and rhyolite. More limited data from other remnants of the original field indicate a similar evolution. In the San Juan field, voluminous early lavas and breccias - mainly alkali andesite, rhyodacite, and mafic quartz latite - were erupted from numerous scattered central volcanoes onto an eroded tectonically stable terrane. They formed mostly during the interval 35 to 30 m.y. ago, but some probably were erupted earlier and others up to several million years later. About 30 m.y. ago, major volcanic activity changed to explosive ash-flow eruptions of quartz latite and low-silica rhyolite that persisted until about 26 m.y. ago. Source areas for the ash flows are marked by large calderas in the central and western San Juan Mountains. Two groups of lavas and associated rocks of intermediate composition intertongue with the ash-flow sequence: (1) quartz latitic lavas that were erupted in and adjacent to caldera structures and are genetically related to the ash-flow activity; and (2) other, generally more mafic lavas and related rocks that are widely distributed without evident structural relation to the ash-flow eruptive centers. The second group apparently represents a continuation of the early intermediate activity into the period of major ash-flow eruption. In the early Miocene the character of volcanism changed notably. Whereas the Oligocene volcanics are predominantly intermediate lavas and related silicic differentiates, the younger rocks are largely a bimodal association of basalt and high-silica alkali rhyolite. Basalt and minor rhyolite were erupted intermittently through the Miocene and Pliocene, and at one time formed a widespread thin veneer over the older volcanic terrane. The marked contrast between the Oligocene intermediate to low-silica rhyolitic magmas and the later basaltic and rhyolitic magmas implies either different conditions of magma generation or processes of differentiation for the two suites. This petrologic change coincides approximately in time with nearby development of the Rio Grande depression, a major rift that is the local expression of widespread late Cenozoic crustal extension. Whatever the cause of the petrologic change, the progression from predominantly intermediate to bimodal basalt-rhyolite volcanism, approximately concurrent with initiation of late Tertiary crustal extension, appears characteristic of Cenozoic volcanism for much of the western interior United States. © 1970, The Geological Society of America, Inc.

Colorado↗

Serpentinization and alteration in an olivine cumulate from the Stillwater Complex, Southwestern Montana

Some of the olivine cumulates of the Ultramafic zone of the Stillwater Complex, Montana, are progressively altered to serpentine minerals and thompsonite. Lizardite and chrysotile developed in the cumulus olivine and postcumulus pyroxenes; thompsonite developed in postcumulus plagioclase. The detailed mineralogy, petrology, and chemistry indicate that olivine and plagioclase react to form the alteration products, except for H 2 O, without changes in the bulk composition of the rocks.

Montana↗

Introduction

Felsic plutonic rocks ranging from dioritic to granitic in composition and from 900 to 550 Ma in age are a major component of the Arabian Shield. These rocks and the potential for associated mineralization have been extensively investigated by the Saudi Arabian Deputy Ministry for Mineral Resources during the past decade in particular. This volume describes the multidisciplinary approach which has been developed, and summarizes results. The classification, distribution, petrology, mineralogy and structure of the felsic plutonic rocks, petrogenetic and metallogenetic concepts and representative examples of mineralization are described. It is concluded that the potential for additional mineral resources is substantial.

Journal of African Earth Sciences↗

Pore-types and pore-network evolution in Upper Devonian-Lower Mississippian Woodford and Mississippian Barnett mudstones: Insights from laboratory thermal maturation and organic petrology

Pore-evolution models from immature organic-matter (OM) -rich Barnett (0.42%R o ) and Woodford (0.49%R o ) mudstones were compared with models previously developed from low-maturity OM-lean Boquillas (Eagle Ford-equivalent) mudstones to investigate whether (1) different mineralogy (siliceous vs. calcareous) exerts different catalytic and sorption effects and influences OM-pore origin and evolution; and (2) different types of macerals show different OM pore evolution history. Laboratory gold-tube pyrolysis, scanning electron microscopy (SEM) and thin-section petrography, organic petrography, and geochemical characterization were used to investigate the role of bulk mineralogy, maceral type, and thermal maturation on OM-pore evolution. Results suggest that mineralogy has little impact on OM-pore development and evolution. Macerals, identified using both SEM (platy OM, particulate OM, organic–mineral admixtures, Tasmanites ) and organic petrology (vitrinite, inertinite, amorphous organic matter [AOM]/bituminite, telalginite [ Leiosphaeridia , Tasmanites ]), do affect the origin and evolution of OM pores owing to differences in chemical compositions, generation kinetics, and activation-energy distributions between Tasmanites , matrix bituminite, and other types of macerals. Leiosphaeridia and Tasmanites in Woodford mudstone samples exhibit a delay in onset and a shorter period of petroleum generation and pore development compared to the matrix bituminite in the Barnett and Woodford mudstone samples. Pre-oil solid bitumen was observed to have migrated into initial primary mineral pore networks at the bitumen generation stage in both Barnett and Woodford samples. At higher levels of thermal maturation, the volume of primary mineral pores decreases and the pore volume composed of modified mineral pores and OM pores becomes greater. Pore evolution and pore-type heterogeneity in these mudstones is a function of the initial mineral pore network, types of kerogen and macerals, and generation kinetics of individual macerals upon thermal maturation.

Oklahoma↗

Paleokarst and reservoir porosity in the Ordovician Beekmantown Dolomite of the central Appalachian basin

A karst-unconformity play at the top of the Ordovician Beekmantown Dolomite is judged to have great petroleum potential in Ohio and adjacent states; wells have high ultimate reserves and large areas remain untested. To better understand the origin, development, and distribution of Beekmantown porosity, we conducted a petrologic-stratigraphic study of cores and thin sections from 15 oil and gas wells. The massive dolomite, characterized by a hypidiotopic-idiotopic texture, formed by the replacement of stacked peritidal carbonate cycles. Secondary porosity occurs at two scales: (1) mesoscopic - breccia porosity, solution-enlarged fractures, large vugs, and caverns, and (2) microscopic - intercrystalline, intracrystalline, molds, small vugs, and microfractures. Mesoscopic pores (providing the major storage capacity in this reservoir) were produced by intrastratal solution and collapse of carbonate layers, whereas microscopic pores (connecting the larger pores) generally formed by the leaching of individual carbonate grains and crystals. Most pore types developed during periods of subaerial exposure across the carbonate bank, tied to either the numerous, though brief falls of relative sea level during Beekmantown deposition or more importantly the prolonged Knox unconformity at the close of sedimentation. The distribution of reservoir-quality porosity is quite heterogeneous, being confined vertically to a zone immediately below the unconformity and best developed laterally beneath buried hills and noses of this erosion surface. The inferred, shallow flow of ground water in the Beekmantown karst, primarily below topographic highs and above a diagenetic base level close to the water table, led to this irregular distribution of porosity.

Carbonates and Evaporites↗

Seismic evidence for a mantle source for mid-Proterozoic anorthosites and implications for models of crustal growth

Voluminous anorthosite intrusions are common in mid-Proterozoic crust. Historically, two end-member models have been proposed for the origin of these anorthosites. In the first model anorthosites derive from fractionation of a mantle source leaving a residue of metagabbro in the lower crust; in the second model anorthosites are the product of partial melting of the lower crust with residual pyroxene and high-grade minerals (i.e. a pyroxenitic and/or metapelitic lower crust). Although a general consensus has developed that the first model provides the best fit to petrological and geochemical constraints, the sparse evidence for mafic and ultramafic counterparts to the anorthosites leaves the issue still unresolved. We use the absolute P-wave velocity and the ratio between P- and S-wave velocities ( V P / V S ) to infer the composition of the lower crust beneath the Marcy Anorthosite (New York State, USA). Seismic refraction data reveal a lower crust 20 km thick, where V P and V P /V S range from top to bottom between 7.0 km s −1 and 7.2 ± 0.1 and 1.84 km s −1 and 1.81 ± 0.02, respectively. Laboratory measurements on rock samples indicate that these seismic properties are typical of plagioclase-rich rocks. Magmatic underplating of basaltic melts is a mechanism to form plagioclase-rich bulk composition for the Grenville crust. At the bottom of the lower crust, increase of P-wave velocity, slight decrease of V P / V S ratios and the presence of a low-reflective seismic Moho are additional observations supporting crustmantle interactions related to magmatic underplating. High P-wave velocity (8.6 km s −1 ) in the upper mantle may indicate that the ultramafic portion (e.g. pyroxenites) of the underplated magma has become eclogite. High average P-wave velocity (6.7 km s −1 ) and V P / V S (1.81), and the exceptional abundance of anorthosites-norites-troctolites among the rocks exposed at the surface, indicate that the Grenville Proterozoic crust may have a unique plagioclase-rich bulk composition. We suggest magmatic underplating, occurring either over a wide time span or with separate syn- and post-collisional magmatic pulses, as being a major crust-forming mechanism operating in mid-Proterozoic time.

Geological Society Special Publication↗

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‘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’ worth of glass compositions for Kīlauea summit eruptions, which, together with expanding databases on prehistoric tephras, provide important constraints on the nature of Kīlauea’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’s. Most summit lavas at both volcanoes, however, lie on olivine control lines having the same olivine composition (Fo 86–87 ). 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’s efforts since Jaggar’s unique descriptions of the Halema‘uma‘u lava lake that existed before 1924. Detailed study of closed-system bodies, including the 1959 Kīlauea Iki, 1963 ‘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‘i and of Lō‘ihi Seamount has revolutionized our understanding of the early history of Hawaiian volcanoes. Observations of Lō‘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’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=14.7–15.0 weight percent) were found along the submarine part of Kīlauea’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↗

On the petrographic distinction of bituminite from solid bitumen in immature to early mature source rocks

The oil-prone maceral bituminite (and its equivalents: ‘amorphous organic matter’, ‘sapropelinite’, ‘amorphinite’, etc.) converts to petroleum during thermal maturation of source rocks, resulting in formation of a mobile saturate-rich hydrocarbon and a polar-rich residue of solid bitumen. Evidence of this transition is preserved in immature to early mature source rocks (e.g., Alum, Bakken, Kimmeridge, New Albany, Ohio shales, among many others), where organic petrography reveals a continuum of textures, reflectance, and fluorescence intensity occurring between bituminite and solid bitumen. Bituminite generally is characterized by high(er) intensity fluorescence, low contrast to the inorganic matrix, lower reflectance (compared to solid bitumen), and heterogeneous wispy or ‘schlieren’ textures. In comparison, solid bitumen generally shows lower intensity or no fluorescence compared to bituminite, a distinct contrast to the mineral matrix which usually includes a gray homogeneous surface of low to moderate reflectance, and may possess void-filling, embayment or groundmass textures suggesting evidence of migration or its in situ exsolution. However, these properties may manifest across a continuous spectrum in a sample or in a single microscope field, often making identification inconclusive. Unambiguous identification is further hampered by sample preparation, e.g., mechanical polish may improve homogeneity of larger accumulations, whereas smaller accumulations, or those sheltered by hard minerals, may appear more heterogeneous, leading to identification of the same organic matter as solid bitumen or bituminite, respectively. The disruptive innovation of ion milling in shale sample preparation leads to increased organic reflectance and surface homogeneity, causing bituminite and other oil-prone macerals, e.g., alginite, to develop a gray reflecting surface which is easy to confuse with solid bitumen, especially when obvious void-filling or embayment textures of the latter are absent. Herein we review distinction of solid bitumen from bituminite and alginite in immature to early mature source rocks, providing examples from nine samples illustrated by typical organic petrography images, including samples from hydrous pyrolysis experiments. Based on a review of the literature, we observe an arbitrary reflectance limit of 0.30% in mechanically polished samples seems to differentiate bituminite (<0.30%) from confident identifications of homogeneous solid bitumen (which otherwise lacks obvious void-filling or identifying embayment textures) as individual macerals on a continuous spectrum in immature and early mature source rocks. Future work conducted by governing bodies such as the International Committee for Coal and Organic Petrology (ICCP) should consider interlaboratory studies conducted on multiple immature source rock samples to develop consensus guidelines for bituminite and solid bitumen discrimination.

International Journal of Coal Geology↗

Characterization of the Sukinda and Nausahi ultramafic complexes, Orissa, India by platinum-group element geochemistry

Samples of 20 chromitite, 14 ultramafic and mafic rock, and 9 laterite and soil samples from the Precambrian Sukinda and Nausahi ultramafic complexes, Orissa, India were analyzed for platinum-group elements (PGE). The maximum concentrations are: palladium, 13 parts per billion (ppb); platinum, 120 ppb; rhodium, 21 ppb; iridium, 210 ppb; and ruthenium, 630 ppb. Comparison of chondrite-normalized ratios of PGE for the chromitite samples of lower Proterozoic to Archean age with similar data from Paleozoic and Mesozoic ophiolite complexes strongly implies that these complexes represent Precambrian analogs of ophiolite complexes. This finding is consistent with the geology and petrology of the Indian complexes and suggests that plate-tectonic and ocean basin development models probably apply to some parts of Precambrian shield areas.

Precambrian Research↗

Depositional setting, petrology and chemistry of Permian coals from the Paraná Basin: 2. South Santa Catarina Coalfield, Brazil

In Brazil economically important coal deposits occur in the southern part of the Paraná Basin, where coal seams occur in the Permian Rio Bonito Formation, with major coal development in the states of Rio Grande de Sul and Santa Catarina. The current paper presents results on sequence stratigraphic interpretation of the coal-bearing strata , and petrological and geochemical coal seam characterization from the South Santa Catarina Coalfield, Paraná Basin. In terms of sequence stratigraphic interpretation the precursor mires of the Santa Catarina coal seams formed in an estuarine-barrier shoreface depositional environment , with major peat accumulation in a high stand systems tract (Pre-Bonito and Bonito seams), a lowstand systems tract (Ponta Alta seam, seam A, seam B) and a transgressive systems tract (Irapuá, Barro Branco and Treviso seams). Seam thicknesses range from 1.70 to 2.39 m, but high proportions of impure coal (coaly shale and shaley coal), carbonaceous shale and partings reduce the net coal thickness significantly. Coal lithoypes are variable, with banded coal predominant in the Barro Branco seam, and banded dull and dull coal predominantly in Bonito and Irapuá seams, respectively. Results from petrographic analyses indicate a vitrinite reflectance range from 0.76 to 1.63 %Rrandom (HVB A to LVB coal). Maceral group distribution varies significantly, with the Barro Branco seam having the highest vitrinite content (mean 67.5 vol%), whereas the Irapuá seam has the highest inertinite content (33.8 vol%). Liptinite mean values range from 7.8 vol% (Barro Branco seam) to 22.5 vol% (Irapuá seam). Results from proximate analyses indicate for the three seams high ash yields (50.2 – 64.2 wt.%). Considering the International Classification of in-Seam Coals, all samples are in fact classified as carbonaceous rocks (> 50 wt.% ash). Sulfur contents range from 3.4 to 7.7 wt.%, of which the major part occurs as pyritic sulfur. Results of X-ray diffraction indicate the predominance of quartz and kaolinite (also pyrite). Gypsum , gibbsite , jarosite and calcite were also identified in some samples. Feldspar was noted but is rare. The major element distribution in the three seams (coal basis) is dominated by SiO 2 (31.3 wt.%, mean value), Al 2 O 3 (14.5 wt.%, mean value) and Fe 2 O 3 (6.9 wt.%, mean value). Considering the concentrations of trace elements that are of potential environmental hazards the Barro Branco, Bonito and Irapuá seams (coal base) are significantly enriched in Co (15.7 ppm), Cr (54.5 ppm), Li (59.3 ppm), Mn (150.4 ppm), Pb (58.0 ppm) and V (99.6 ppm), when compared to average trace elements contents reported for U. S. coals. Hierarchical cluster analysis identified, based on similarity levels, three groups of major elements and seven groups of trace elements. Applying discriminant analyses using trace and major element distribution, it could be demonstrated that the three seams from Santa Catarina show distinct populations in the discriminant analyses plots, and also differ from the coals of Rio Grande do Sul analyzed in a previous study.

Santa Catarina↗

Chemical variability in the Lakeview Mountains pluton, southern California batholith: A comparison of the methods of correspondence analysis and extended Q-mode factor analysis

An extended method of Q -mode factor analysis that has been described previously offers a number of important advantages over conventional Q -mode factor analysis and correspondence analysis when applied to compositional data. Among these are the ability to compute the compositions, in the original units of the data, represented by the reference axes. The only special requirement of the data is that the values for each observation sum to a constant. Mathematically derived reference axes, such as the principal-components and varimax axes, commonly represent compositions that are partly negative. Even where no negative values are present, these compositions are comparatively difficult to interpret in petrologic terms and impossible or inappropriate to include in petrogenetic models. A model has been developed for the Lakeview Mountains pluton which employs vectors representing the compositions of melanocratic schlieren, leucocratic schlieren, and inclusions as the reference axes. When the effect of the inclusions is removed, the compositional zoning in the pluton is like that found in otherwise similar plutons in the Sierra Nevada batholith. The genetic implication of the model is that the inclusions were separated from the magma at least in its marginal parts. In the central part of the pluton, the inclusions were either separated to a lesser extent than in the marginal parts, or were reincorporated into the magma.

California↗