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Ryan J. McAleer

Publications and source records attributed to Ryan J. McAleer.

At least 19 recordsLinked to original sources

Microfocus X-ray computed tomography to evaluate ostracode shell density and other metrics for monitoring ocean acidification in the Arctic Ocean

Ocean acidification (OA) poses a significant threat to the ability of marine calcifying organisms—such as mollusks, corals, crustaceans, and plankton—to form and maintain their calcium carbonate-based shells. While some species show greater sensitivity to OA than others, the impacts on benthic marine calcifiers remain inadequately understood. This study investigates the shell density, weight, and thickness of the ostracode species Paracyprideis pseudopunctillata (subphylum Crustacea), which inhabits the continental shelves of the Arctic Ocean. Using microfocus X-ray computed tomography (microXCT) scans, we generated detailed morphometric measurements of specimens collected from both surface and down-core sediment samples to assess variations in shell properties over time. To our knowledge, this is the first study to examine the natural variability of ostracode shell characteristics in a specific region over an extended time period. For each specimen, we calculated a CT number, an index of relative calcium carbonate density, using a previously published equation. Our findings show that most living specimens of P. pseudopunctillata in the Beaufort Sea showed no overt signs of OA-related shell compromise or degradation. Shell density remained consistent between 1969 and 2018 CE, with consistent CT numbers suggesting that corrosive bottom waters are not a persistent feature in this area of the Beaufort Sea continental shelf. This is supported by a timeseries of discrete pH and carbonate saturation measurements. To help quantify diagenetic impacts on ostracode shells, we compared this calibration dataset with measurements of well-preserved adult specimens from downcore intervals of a box core (MR22, MT1, 1-29 cm) and a multicore (HLY1302 MC29, 25-35 cm), both collected from the same location, representing 2018 to 1955 CE and 1953 to 1925 CE, respectively. The CT numbers from these specimens were also consistent, which confirmed the preservation state of most specimens. However, several specimens had low CT numbers, and these shells show surficial evidence of post-mortem diagenesis. We aimed to quantify the extent of diagenesis, which has important implications for paleoenvironmental reconstructions. These findings provide important baseline data for understanding the variability of modern ostracode shell density of fossil and alive-collected specimens.

Deep Sea Research Part II: Topical Studies in Ocea↗

Evidence for a biological origin of uranium-rich carbon masses within the Ediacaran Salt Range Formation of Pakistan

Thucholites are unique organic structures found in igneous and sedimentary rocks composed of a U-C-rich interior enclosed by an organic outer shell. Their formation and occurrence have perplexed scientists for over 100 years. Typically, thucholites are sparse in sedimentary rocks but where found in abundance, they may be the result of rapid paleoecological disruptions, e.g., volcanic ashfall. Here, we evaluated thucholites from the Ediacaran Salt Range Formation of the Indus Basin in Pakistan using field emission scanning electron microscopy (FESEM) and nanoscale secondary ion mass spectroscopy (NanoSIMS) to propose a two-stage mechanism for thucholite development. NanoSIMS results suggest organic matter in thucholite cores formed by biological fractionation (represented by the presence of lighter 13 C/ 12 C and 34 S/ 32 S) while the outer organic mantle formed via radiolysis-induced polymerization. FESEM elemental analysis confirms compositional differences between the two thucholite components (core and mantle), further implying their contrasting origins. Dimensional comparison of thucholite cores and their U-bearing mineral morphologies to ancient and modern U-biomineralized microbes suggests that the thucholite cores formed from metal-biological interactions. The presence of volcanogenic biotite, alkali feldspar, and clay spherules (interpreted as devitrified volcanic glass) with thucholite suggests that the thucholite cores in the Salt Range Formation are biological responses to rapid paleoenvironmental change from volcanic eruption which preserved the fossilized morphologies of Proterozoic microorganisms.

Salt Range↗

Petrography and mineralogy of selected pre-Middle Jurassic basement rocks beneath the Atlantic and Gulf Coastal Plains in Florida

Florida is covered by flat-lying sedimentary strata of the Atlantic and Gulf Coastal Plains. These strata have accumulated since Middle Jurassic time. The pre-Middle Jurassic, or basement, rocks that underlie the Coastal Plain in Florida are known only from drill cores and cuttings recovered from a relatively small number of boreholes. This data report presents petrographic observations and the results of X-ray diffraction analyses of basement rocks from 18 boreholes across Florida in support of the identification, discrimination, and correlation of units for a subcrop geologic map of pre-Middle Jurassic rocks composing Florida’s sub-Coastal Plain geology.

Florida↗

Preliminary geologic map of the Sparta East, Sparta West, and parts of the Glade Valley and Whitehead 7.5-minute quadrangles, North Carolina and Virginia, and the epicentral area of the August 9, 2020, Mw 5.1 earthquake near Sparta, North Carolina

Introduction New bedrock and surficial geologic mapping in the Sparta East, Sparta West, and parts of the Glade Valley and Whitehead 7.5-minute quadrangles, North Carolina and Virginia, investigates the geologic framework and causative mechanisms of the August 9, 2020, Mw 5.1 earthquake near Sparta, North Carolina. The mapping documents (1) the coseismic surface rupture from the 2020 earthquake and related brittle structures in the bedrock; (2) the fault contact between the western Blue Ridge and eastern Blue Ridge; (3) lithostratigraphy in the Lynchburg Group, Ashe Metamorphic Suite, and Alligator Back Metamorphic Suite; (4) the nature of the contact between the Lynchburg Group, Ashe Metamorphic Suite, and Alligator Back Metamorphic Suite; and (5) surficial deposits.

North Carolina, Virginia↗

Geochemical disequilibrium at the brittle-ductile transition

We investigate the microtextural, microchemical, and isotopic effects of late-stage ductile deformation in quartzite mylonites and kyanite–muscovite–quartz veins from the Raft River shear zone (Utah). Quartz microstructures record pervasive disequilibrium, expressed by unannealed features including undulatory extinction, deformation lamellae, and poorly defined fabrics, typical of waning deformation in shear zones. Microchemical disequilibrium is best preserved in kyanite quartzites, where CL-zoned kyanite records repeated fractures, overgrowth, and mineral precipitation, and in muscovite from muscovite-poor quartzite mylonites that shows minor-element zoning consistent with syn-deformational overgrowth on detrital cores. In contrast, muscovite from muscovite-rich kyanite quartzites exhibits minimal chemical zoning. These microchemical variations correlate with 40 Ar/ 39 Ar age systematics. Chemically zoned muscovite preserves variable single-step ages, including ∼150 Ma ages, reflecting retention of detrital cores. In contrast, syndeformational muscovite consistently yields Miocene ages, indicating recrystallization and new growth below argon closure temperatures that reset inherited isotopic signatures. Similar trends are observed in quartzite mylonites, where increasing quartz recrystallization and stronger crystallographic preferred orientations occur toward deeper structural levels. Together, these observations indicate increasing retrograde deformation and recrystallization with depth in the Raft River shear zone and demonstrate that strain-driven recrystallization exerts a first-order control on muscovite ages. We suggest that apparent thermochronologic gradients in retrograde shear zones may reflect recrystallization gradients rather than temperature gradients. Where cooling limits the thermal driving force for recrystallization, isotopic relics are preserved, and local deformation and fluid availability control re-equilibration. Consequently, isotopic disequilibrium—particularly in the 40 Ar/ 39 Ar system—may be the rule rather than the exception of retrograde tectonic environments.

Idaho, Utah↗

Bedrock geologic map of the Eagle Lake quadrangle, Essex County, New York

The bedrock geology of the 7.5-minute Eagle Lake quadrangle, Essex County, New York, consists of deformed and metamorphosed Mesoproterozoic gneisses of the Adirondack Highlands unconformably overlain by weakly deformed lower Paleozoic sedimentary rocks of the Champlain Valley. The Mesoproterozoic rocks occur on the eastern edge of the Adirondack Highlands and represent an extension of the Grenville Province of Laurentia. Granulite facies Mesoproterozoic paragneiss, marble, and amphibolite hosted the emplacement of an anorthosite-mangerite-charnockite-granite (AMCG) suite, now exposed mostly as orthogneiss, at approximately 1.18–1.15 giga-annum (Ga, billion years before present). The earliest of four phases of deformation (D1) predated AMCG magmatism and is characterized by gneissosity, rarely preserved F1 isoclinal folds, and migmatite in the paragneiss host rocks. A sample of hornblende quartz syenite from the AMCG suite, collected from an abandoned railroad cut on Old Furnace Road, yielded a U-Pb zircon age of 1,149±10 million years before present. D2 deformation produced a composite penetrative gneissosity, migmatite, and isoclinal F2 folds. Towards the end of D2, felsic magmatism (including the regionally extensive Lyon Mountain Granite Gneiss, abbreviated “LMG”) spread by penetrative migration as semiconcordant alkali feldspar granite sheets subparallel to S2 into the previously deformed lithologies. The LMG crystallized at approximately 1.15 to 1.14 Ga and displays synkinematic F2 folds thus constraining the time of D2 deformation. Exhumation of the Marcy anorthosite began during D3 along a mylonitic extensional detachment, as a type of core complex. Protracted D3 produced F3 folds exhibited in regional domes and basins, such as the Hammondville antiform, reactivation of the S2 foliation, partial melting, metamorphism, metasomatism, iron ore remobilization, and intrusion of magnetite-bearing pegmatite both as layer-parallel sills and crosscutting dikes. D4 created NE- and NW-trending boudinage, local high-grade ductile shear zones, and crosscutting granitic pegmatite dikes. Kilometer (km)-scale lineaments readily observed in lidar data are Ediacaran mafic dikes and Phanerozoic brittle faults. Lower Paleozoic rocks are part of the Early Cambrian to Late Ordovician great American carbonate bank on the ancient margin of Laurentia. The Potsdam Sandstone preserves the Cambrian stratigraphy in outliers above the Great Unconformity. The Paleozoic rocks are weakly folded and block faulted. Parts of the quadrangle are covered by undifferentiated glacial deposits, but much of the quadrangle contains only a variably thick, veneer of unmapped glacial till over significant areas of exposed bedrock. The map also shows waste rock piles and locations of historical mining operations. This study was undertaken to improve our understanding of the bedrock geology in the Adirondack Highlands, establish a modern framework for 1:24,000-scale bedrock geologic mapping in the Adirondack Mountains, and provide a modern context for historical mines. This Scientific Investigations Map of the Eagle Lake 7.5-minute quadrangle consists of a map sheet, an explanatory pamphlet, and a geographic information system database that includes bedrock geologic units, faults, outcrops, and structural geologic information. The map sheet includes a bedrock geologic map, a correlation of map units, a description of map units, an explanation of map symbols, and two cross sections. The explanatory pamphlet includes a discussion of the geology.

New York↗

Release and recapture: Limited carbon mobilization in sediment adjacent to Central Atlantic Magmatic Province sills, Florida, USA

Large Igneous Provinces (LIPs) are associated with dramatic changes to the Earth system; their rapid release of carbon may initiate catastrophic climatic changes causing mass extinction. This carbon release is often associated with volcanic emissions, yet metamorphic carbon production is poorly constrained. Metamorphic carbon devolatilization occurs as intrusions interact with host sediment, potentially releasing substantial sedimentary carbon. While this process has been modeled, few studies use an observational approach. Here, we apply geochemical analysis, petrographic analysis, Raman spectroscopy, vitrinite reflectance, and thermodynamic modeling to understand carbon devolatilization in sediment adjacent to Central Atlantic Magmatic Province basaltic intrusions using two boreholes that penetrate the Florida basement. We find geochemical and petrographic evidence for CO 2 release from carbonates below a 10 m thick sill, with upward fluid transport and recapture of mobilized CO 2 at the top of the sill. Ultimately, we estimate 220 mols/m 2 to 9900 mols/m 2 of carbon were mobilized from sedimentary carbonate. Uncertainties in the extent of re‑carbonation suggest that anywhere from 0 mols/m 2 to 7100 mols/m 2 may have escaped to the surface. We find little evidence of organic carbon mobility, due partly to the increased activity of CO 2 from carbonate devolatilization. Discrepancies between measured temperatures and 1D thermal models suggest complexities in heat transport through aqueous pore fluid flow and short (hundred to thousand year) heating timescales. These results highlight that further field-based study can help clarify the roles that heating timescales, fluid flow, sediment chemistry, and other factors play in releasing and capturing carbon during LIP emplacement.

Florida↗

Pre-Acadian tectonics of the eastern Orange-Milford Belt, south-central Connecticut

This excursion presents a reinterpretation of mapping and new analytical data from the eastern Orange-Milford belt (OMB) in south-central Connecticut. The OMB is a fault-bound terrane of argillites and mafic rocks of anomalously low metamorphic grade—and of poorly constrained ages and tectonic affinity—wedged between kyanite/sillimanite-grade peri- Laurentian rocks to the west and anatectic peri-Gondwanan rocks to the east (Fig. 1A). Our data demonstrate that Ordovician(?) igneous and sedimentary rocks of the OMB were variably metamorphosed in the Ordovician and Silurian but escaped regionally pervasive, high-grade Devonian and later metamorphism. Previous interpretations (Fritts 1963a, 1965a, 1965b; Burger, 1967; Burger and others, 1968; Rodgers, 1985) described these rocks as a conformable sequence of low-grade, Ordovician to Devonian metasediments and metavolcanics. Our results reveal that the “metavolcanics” are not extrusive rocks but rather slivers of lower oceanic crust with complicated high- and low-grade metamorphic fabrics, intruded by a swarm of Silurian sheeted basalt dikes, and in fault contact with the surrounding metasediments. The purpose of this trip is to show evidence of early Paleozoic (Taconic) deformation and metamorphism preserved in rocks of the eastern OMB. These rocks remained shallow, cool, and sufficiently dry during the regionally dominant Acadian and Alleghanian orogenies to have avoided significant overprinting. As such, these rocks serve as windows into a geologic history otherwise unavailable between anatectic rocks of the peri-Gondwanan Bronson Hill, Avalon, and Gander terranes east of the Hartford basin and sillimanite-grade rocks of the peri-Laurentian Hartland and gneiss dome belts west of the OMB. We present major and trace element geochemistry including rare-earth element patterns for all mafic units in the eastern OMB as well as 40 Ar/ 39 Ar age spectra of amphibole, muscovite, and K-feldspar from rocks of the Maltby Lakes complex (of Deasy and others, 2017), Savin Schist, and Wepawaug Schist. Our evidence demonstrates that the units of the OMB have been assembled by faulting or intrusion, and that no stratigraphic relationships exist between the argillaceous schists and the metaigneous rocks.

Connecticut↗

Bedrock geologic map of the Bellows Falls 7.5- x 15-minute quadrangle, Windham and Windsor Counties, Vermont, and Sullivan and Cheshire Counties, New Hampshire

Introduction The bedrock geology of the Bellows Falls 7.5- x 15-minute quadrangle, Vermont and New Hampshire, consists of polydeformed Ordovician to Devonian metasedimentary, metavolcanic, and metaplutonic rocks of the Connecticut Valley trough, Bronson Hill anticlinorium (or Bronson Hill terrane), and the Central Maine terrane. Previous work in this area includes a 1:62,500-scale published map and text (1946), State geologic maps of New Hampshire (1997) and Vermont (2011), and various maps and reports presented largely as parts of field trip guidebooks. A provisional open-file map of the geology of the Vermont part of the Bellows Falls 7.5- x 15-minute quadrangle, completed in 1997, is incorporated and revised on this map based on additional fieldwork. This study recognizes three major structural levels from west to east and from lowest to highest: (1) autochthonous rocks of the Connecticut Valley trough; (2) allochthonous rocks of the New Hampshire sequence and Bronson Hill arc in the Monroe thrust sheet (or nappe), including the Skitchewaug nappe; and (3) allochthonous rocks of the Fall Mountain thrust sheet or nappe.

New Hampshire, Vermont↗

Geochemical and tectonic evolution of the Ordovician Bronson Hill arc and Silurian and Devonian Connecticut Valley–Gaspé trough: Eastern Vermont and western New Hampshire, USA

We present major and trace element whole-rock geochemistry of 94 samples from the Bronson Hill arc (BHA) and Connecticut Valley–Gaspé trough (CVGT). These data, when combined with recent zircon U-Pb geochronology and a reexamination of existing whole-rock geochemistry, enable a new analysis of the tectonic history of the ancient Laurentian-Ganderian margin in the northern Appalachians of New England, USA, and southeastern Canada. The whole-rock geochemical data from the Ordovician BHA in western New Hampshire indicate that metamorphosed extrusive and intrusive rocks share the same temporally variable geochemical fingerprint. Mafic and felsic rocks form a bimodal distribution and plot as island arc magmas on geochemical discrimination diagrams. Approximately 80% of mafic greenstone and amphibolite samples plot as island arc tholeiites with a subset of samples that trend toward a more within-plate basalt geochemical signature. Where ages are known, older felsic rocks (ca. 475–460 Ma) in the BHA tend to be more sodic and less potassic than their younger (ca. 460–445 Ma) counterparts, and the geochemical results trend from volcanic arc granites toward syn-collisional granites through time. Prior to recent geochronology, it was thought that an age gap existed between the island arc magmas and the syn collisional granites. This led to the separation of felsic plutons into the predominantly older trondhjemitic magmas assigned to the Ammonoosuc Volcanics and a younger suite of granites designated as the Oliverian Plutonic Suite. This age gap was thought to represent a flip in subduction polarity which would also account for observed changes in pluton chemistry. With the addition of more recent U-Pb isotopic age data, we now know there is a continuum of ages, and a polarity flip is no longer required. When the isotopic ages are combined with the new geochemical data presented here, they suggest that as the BHA approached and collided with Laurentia ca. 455 Ma, continental material was assimilated into the magma, and there was a transition from trondhjemite to granodiorite and granite magmas in felsic rocks and from island arc tholeiite toward more alkali-rich basalt with a continental signature in mafic magmas. The similarities in whole-rock and trace element geochemistry, rock type, and range of isotopic ages from the Ammonoosuc Volcanics, Partridge Formation, and Oliverian Plutonic Suite, suggest they originated from the same magma source and were part of one evolving island arc system that persisted throughout the Ordovician, and the need to separate the Oliverian Plutonic Suite from the Ammonoosuc Volcanics is not necessary. Most magmatism in the BHA ceased ca. 440 Ma. Following the Taconic orogeny, Silurian basin development was widespread along the length of the Laurentian-Ganderian suture. In New England and Québec, this resulted in the formation of the CVGT. The BHA and the CVGT are generally studied separately: the BHA in the context of arc-continent collision during the Taconic orogeny, and the CVGT as it relates to post-orogenic extension or the distal effects of the Salinic disturbance. When viewed collectively, the igneous geochemistry of the BHA and CVGT reveals an overlap between the waning stages of Taconic orogenesis and the onset of Silurian to Devonian basin development in the northern Appalachians. Metamorphosed bimodal volcanic and intrusive rocks are present in the CVGT (ca. 434–407 Ma) and Silurian cover sequence, which unconformably overlies the BHA. Mafic rocks in the CVGT are mostly tholeiitic basalts with a subset of alkali basalt in the Waits River Formation. Tectonic discrimination diagrams show that the mafic rocks are a mix of mid-ocean ridge basalt to within-plate basalt. The felsic rocks in the CVGT are mostly metamorphosed volcanic rocks that vary from island arc granite to within-plate granite. The geochemical signature of the CVGT is consistent with a post-collisional intra-arc basin, where slab breakoff or crustal attenuation played a key role before transitioning to a deepening foreland basin at the beginning of the Acadian orogeny.

New Hampshire, Vermont↗

Geologic map of the Buckner 7.5-Minute quadrangle, Louisa County, Virginia

The Buckner 7.5-minute quadrangle straddles three terrane boundaries in the Piedmont Physiographic Province in central Virginia: the Chopawamsic terrane, the Elk Hill Complex, and the Goochland terrane. In much of the map area, the Elk Hill Complex separates the Chopawamsic and Goochland terranes. Rocks of the Chopawamsic terrane include Ordovician metavolcanic and metasedimentary rocks of the Chopawamsic Formation, Ordovician to Silurian granodiorite sheet intrusions, and Paleozoic mafic intrusions. Silurian to Devonian rocks of the Quantico Formation, mostly garnet-mica schist, crop out in the northwesternmost part of the map area, and are in unconformable contact with rocks of the Chopawamsic Formation on the southeastern limb of the Quantico synclinorium. The main map unit in the Elk Hill Complex is Neoproterozoic mica gneiss, which is in pre-metamorphic fault contact with rocks of the Chopawamsic Formation to the west. The main map unit of the Goochland terrane is the Maidens Gneiss. Except for Jurassic diabase dikes, all rocks on the Buckner 7.5-minute quadrangle were metamorphosed to amphibolite facies during the Alleghanian orogeny and preserve multiple compositional and phyllosilicate penetrative foliations. Evidence of amphibolite-facies metamorphism during the Taconic orogeny is preserved in rocks of the Elk Hill Complex. The entire width of the Maidens Gneiss on the Buckner 7.5-minute quadrangle is within the Spotsylvania high-strain zone and amphibolite-facies mylonitic textures are pervasive. Quartz veins and Jurassic diabase dikes crosscut all older rocks of the quadrangle. Multiple levels of terrace deposits are present along and near the major streams of the quadrangle. The lower terrace deposits are likely remnants of former positions of the Little River on the landscape, whereas higher deposits may be remnants of former deposits of the Atlantic Coastal Plain that covered this portion of the Piedmont Province. A linear cluster of aftershocks from the magnitude 5.8 earthquake that occurred near Mineral, Virginia, in 2011 defines the Fredericks Hall fault, which is at depth on the Buckner quadrangle. Most of the aftershocks occurred in the core of the Elk Creek antiform and have no relation to faults mapped at the surface. Several abandoned crushed stone and building stone quarries, as well as a mica prospect, exist in the quadrangle.

Virginia↗

Pocoshock Creek Gneiss and redefinition of the Petersburg Granite, central-eastern piedmont of Virginia

The Petersburg Granite (sensu lato) was formerly interpreted to be a single late Paleozoic composite batholith in the central-eastern part of the Piedmont Physiographic Province of Virginia. Detailed mapping beginning in the mid 2000s resulted in the subdivision of these voluminous granitic rocks into five units—layered granitic gneiss, foliated granite, porphyritic granite, subidiomorphic (equigranular) granite, and pegmatitic granite. U-Pb zircon geochronology demonstrate that foliated granite and layered granitic gneiss currently assigned to the batholith are 100 million years (m.y.) older, and yield Silurian to Devonian ages (ca. 425 mega-annum (Ma) to ca. 403 Ma). We propose the name Pocoshock Creek Gneiss for these strongly foliated and layered gneisses. Geochronologic data also require redefinition of the Petersburg Granite (sensu stricto). Massive equigranular and porphyritic rock types of the Petersburg Granite (sensu stricto) are geochemically distinct from a subset of Pocoshock Creek Gneiss samples. Massive equigranular and porphyritic rock types are similar to another, more granitic subset of the Pocoshock Creek Gneiss, which indicates different magma sources for the Petersburg Granite (sensu stricto) and Pocoshock Creek Gneiss but also likely indicates assimilation of Pocoshock Creek Gneiss during late Paleozoic intrusion of these Petersburg Granite (sensu stricto) rock types. Equigranular granite southwest of Petersburg, Virginia is 15–20 m.y. older than porphyritic granite, massive granite, and monzodiorite (ca 300 Ma) near Richmond, Virginia. The Petersburg Granite (sensu stricto) consists of two regional plutons—the northern Richmond pluton and the southern DeWitt-Sutherland pluton. The DeWitt-Sutherland pluton of Early Pennsylvanian age is separated from Late Pennsylvanian to early Permian granite of the Richmond pluton by a map scale septum of Pocoshock Creek Gneiss. Geochemical analyses of 15 samples of Pocoshock Creek Gneiss are compared to other igneous suites throughout the Appalachian orogen. Whole rock geochemistry shows elevated average thorium and uranium values in porphyritic granite compared to massive equigranular granite and Pocoshock Creek Gneiss and suggest that homes and businesses built on that rock type of the Richmond pluton may be most at risk for uranium and (or) dissolved radon in groundwater or radon gas in confined spaces.

Professional Paper↗

Properties of solid bitumen formed during hydrous, anhydrous, and brine pyrolysis of oil shale: Implications for solid bitumen reflectance in source-rock reservoirs

Solid bitumen reflectance (BR o in %) is widely used as a thermal maturity proxy in source-rock reservoirs, yet solid bitumen texture and physical attributes may be affected by varying environmental constraints during its formation, e.g., water saturation, mineral catalysis, or salinity. Herein we investigated the development of solid bitumen properties during artificial maturation using three diverse (lacustrine to marine) oil shale samples containing abundant amorphous H-rich sedimentary organic matter (bituminite). The oil shales were treated via pyrolysis (320 °C, 72 h) using hydrous, anhydrous, and brine conditions, causing the development of a newly formed solid bitumen in the experiment residues from the thermal conversion of bituminite. The properties of the newly formed solid bitumen then were evaluated via geochemical screening tests, optical and electron microscopy, and infrared spectroscopy. Experimental residues also were treated via solvent extraction, allowing characterization of the effects of extraction on solid bitumen. Results showed that bituminite with higher resin and asphaltene components evolved to a solid bitumen with higher reflectance (as a percentage of the original value) when exposed to the same heat treatment, relative to bituminite with higher saturate and aromatic components. Aromatization of solid bitumen also was generally more pronounced in the presence of deionized water relative to anhydrous conditions, supporting prior observations. These results suggest the compositions of primary sedimentary organic matter, and the local concentration of water, affect the development of solid bitumen during thermal advance, potentially explaining the origin of multiple solid bitumen populations with varying reflectance in source-rock reservoir samples or in a single microscope field. Experiments using brine were inconclusive regarding enhanced/decreased aromatization, which could be attributed to the salinities of the brines used in the tests. Extraction of residues caused a consistent increase in BR o values, suggesting that migrating or expelled oils could cause an increase in BR o via natural solvation and absent an increase in temperature. This work provides insights into the development and evolution of BR o in source-rock reservoirs as a function of the composition of the original bituminite and changing environmental conditions, with potentially broad application for petroleum prospecting and resource estimation.

Colorado↗

Evaluation of solid bitumen created from marine oil shale bituminite under hydrous and anhydrous pyrolysis conditions

To test the influence of environmental conditions on aromaticity of solid bitumen generated during petroleum generation, four organic-rich (26–36 wt% total organic carbon) oil shale samples collected from the Neoproterozoic–Lower Cambrian restricted marine Salt Range Formation in the upper Indus Basin, Pakistan, were pyrolyzed under hydrous and anhydrous conditions. Experiments used closed system batch reactors at subcritical water temperatures between 300 and 370°C for 72 h. Thermal conversion of bituminite in the Salt Range oil shales created a newly formed solid bitumen, similar to previous observations from experiments on the Eocene lacustrine Green River Formation Mahogany zone oil shale. Newly formed solid bitumen in the Salt Range Formation oil shales generally has higher reflectance (R o ) in hydrous residues compared to anhydrous experiments subjected to the same time-temperature conditions, also similar to prior observations. This finding supports the hypothesis that radical disproportionation is favored in the presence of hydrogen contributed by water, promoting aromatization in the solid bitumen residue with concomitant increased expulsion of saturated hydrocarbons. Indigenous solid bitumen (and vitrinite in a comparison sample) also shows higher reflectance values in hydrous versus anhydrous residues, indicating that additional aromatization in the presence of exogenous hydrogen occurs both in newly formed organic matter and in organic matter that is present throughout the experiment. Despite similarities in their bulk rock geochemical screening parameters, R o evolution shows different trajectories amongst the four Salt Range oil shales, suggesting as-yet undetermined differences in kinetic properties which are probably related to differences in a priori chemical composition. These results have implications for the use of solid bitumen reflectance (BR o ) as a thermal proxy, suggesting BR o values and appearance could vary as a function of the concentration of water. Variation in water concentration may be present at the reservoir or formation scale, but may also be present at a much finer scale in tight oil shales where permeability is several orders of magnitude lower than conventional reservoirs. Therefore, local variations in the presence of water potentially could explain substantial variation in BR o values and appearance in closely spaced source rock samples and even within an individual microscope field.

Journal of Analytical and Applied Pyrolysis↗

Reaction kinetics and accelerant effects of sulfides in early mature hydrocarbon generation using hydrous pyrolysis

Hydrocarbon generation in organic-rich sediments is influenced by the molecular organic composition and relative abundance of associated minerals. Certain mineral-derived elements act as catalysts and reaction intermediaries, facilitating early-stage hydrocarbon formation in potential source rocks. This study investigated the role of sulfur contributed from pyrite as an accelerant in thermal reaction, focusing on its effects on early maturation and consequent hydrocarbon generation from gilsonite (low-sulfur solid petroleum). Hydrous pyrolysis (HP) experiments were conducted on mixtures of gilsonite and pyrite in varying ratios (1:0.1, 1:0.5, 1:1, 1:2, and 1:10 w/w gilsonite:pyrite) at 320, 350, and 370 °C for 72 h. Untreated and thermally altered residues were analyzed using solid bitumen reflectance (BR o , %), total organic carbon (TOC) content, programmed temperature pyrolysis, scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), and X-ray diffraction (XRD) to evaluate the potential accelerant role of pyritic sulfur in hydrocarbon formation. The results show HP residues at 320 and 350 °C with greater pyrite concentrations had higher BR o , while reflectance values were similar in the 370 °C residues, regardless of pyrite concentration, suggesting enhanced reaction at lower thermal conditions. Increasing pyrite content systematically decreased hydrogen index (HI) values while increasing the transformation ratio (TR) and production index (PI), indicating enhanced conversion of organic matter to hydrocarbons with increasing pyrite concentrations. Gas yields increased with pyrite addition, particularly at 350 °C, confirming secondary cracking effects. However, gas production stabilized or declined at higher pyrite loadings (1:10), suggesting alternative reaction pathways such as coke formation. Our data indicate the presence of pyrite lowers the activation energy for thermal cracking, shifting peak experimental hydrocarbon generation temperatures downward by 20–30 °C, with the most pronounced accelerant effects observed at moderate pyrite concentrations (1:0.5 and 1:1). The thermodynamic framework reveals that pyrite stability is influenced by experimental conditions, with pyrrhotite formation favored in the presence of gilsonite due to reduced oxygen fugacity. Pyrite transformation to pyrrhotite, as observed through XRD, SEM-EDS, and predicted by thermodynamic data, further supports the accelerant role of S, as pyrrhotite exhibits a higher hydrogen transfer potential, promoting early oil generation. These findings highlight the importance of pyrite in modulating hydrocarbon generation pathways in organic-rich systems.

Journal of Analytical and Applied Pyrolysis↗

Geochemistry and spatial distribution of Neoproterozoic dike swarms from the northwestern tip of the Arabian-Nubian Shield: Implications for crustal extension

Ediacaran dike swarms in the Arabian-Nubian Shield (ANS) provide key insights into post-collisional tectonics and magmatism. This study presents new chemical data, two 40 Ar/ 39 Ar ages, and spatial distribution analysis for dike swarms in the northernmost ANS exposures in SW Jordan. Hornblende from a lamprophyre sill intruding the Saramuj Conglomerate yielded a plateau age of ∼592 ± 3 Ma, interpreted as the crystallization age of the sill. Micro-cores of sericite-rich domains in altered plagioclase phenocrysts from a dolerite dike intruding ∼586 Ma alkali granite produced ages of ∼580–570 Ma, interpreted as hydrothermal alteration ages, constraining dike emplacement to 586–580 Ma. The geochemistry of investigated dikes varies from alkaline to subalkaline and crosscuts calc-alkaline magmatic rocks. This transition reflects a shift from compression to extension (∼610-590 Ma), lithospheric thinning, and changes in mantle sources. After 590 Ma, magmatism became exclusively alkaline, forming A-type granitoids and dolerites, marking a shift to extensional magmatism. Dikes predominantly follow NE-SW and E-W orientations, with rare N-S, NW-SE, and WNW-ESE trends, suggesting a major horizontal extension direction from NW-SE to N-S. Dike density ranges from 5 to 13 %, averaging ∼9 %, with crustal extension estimates of 9–23 %, averaging 16 %. No correlation was found between dike composition, orientation, or order of emplacement, indicating consistent stress orientation during the final stage (605-580 Ma) of ANS evolution.

Journal of African Earth Sciences↗

Nanometer-scale relationships between sedimentary organic matter molecular composition, fluorescence, cathodoluminescence, and reflectance: The importance of oxygen content at low thermal maturities

Molecular characterization of sedimentary organic matter (SOM), termed macerals, is a common goal when seeking to understand petroleum generation as well as other geologic processes in deep time. However, unambiguous measurement of discrete macerals is challenging due to the small size of organic particles in sedimentary rocks, the proximity of different organic matter types to one another, mineral-organic matter interactions, and maceral mixing that occurs during SOM isolation prior to ex situ analysis. The recent advent of infrared spectrometers capable of nanometer-scale resolution and the application of these technologies to geologic samples has enabled advances in rapid, in situ molecular characterization of SOM allowing for insights into paleoenvironmental processes, such as organic matter productivity and preservation, among others. Here we employ one such technology, optical photothermal infrared (OPTIR) spectroscopy, to map SOM functional group distributions at 500-nm resolution in a sample from the Lower Cretaceous Sunniland Limestone of the South Florida Basin. Examined fields of view include occurrences of amorphous organic matter (AOM), inertinite, micrinite, solid bitumen, telalginite, and vitrinite. OPTIR data from these macerals are compared against traditional organic petrographic data from the same organic grains including fluorescence intensity and white light reflectance as well as against cathodoluminescence response, an emerging organic petrographic approach. Maceral oxygen content (using carbonyl functional group abundance as a proxy) is observed to vary widely between maceral types but correlates strongly with fluorescence and cathodoluminescence intensity as well as against reflectance. These findings highlight the important role that oxygen content plays in determining the optical properties of SOM and further demonstrate the ability of OPTIR to discriminate subtle molecular differences between SOM types.

Organic Geochemistry↗

Deformation by pressure solution and grain boundary sliding in a retrograde shear zone in southern New England, USA

Alleghanian phyllonites in a shear zone in southern New England were formed by the retrogression and hydration of a high-grade Acadian pelitic schist. The retrogression was locally incomplete, resulting in both heterogeneous mineralogy and mineral compositions, and in many arrested reaction textures. These features, documented by backscattered electron and element map imaging, and by 40 Ar/ 39 Ar dating, provide a record of the processes active as the schist was converted to a phyllonite. On the margins of the shear zone relic biotite and garnet grains survive but are partially replaced by chlorite. Relic high-grade muscovite flakes containing up to 35 % paragonite (pg) also persist but are entrained in swarms of pg-poor muscovite flakes producing folia with an anastomosing network of muscovite grains of variable composition. Single crystals of pg-rich muscovite are truncated by muscovite in successively younger cross-cutting folia that contain decreasing pg contents, falling to <5% pg in the youngest folia. In the core of the shear zone all high-grade minerals are destroyed, but recrystallization continues with earlier greenschist facies folia replaced by lower grade and pg-poorer muscovite in younger folia. Muscovite grains in truncated folia are commonly kinked and selective recrystallization of muscovite in kink bands to pg-poor-compositions demonstrates that strain energy helped drive recrystallization. The boundaries of these new pg-poor muscovite folia are sharp, and truncations indicate that grain boundary sliding (GBS) involved dissolution. GBS also enabled folding by flexural slip along muscovite grain boundaries. Fold amplitudes increased as chlorite dissolved from fold limbs precipitated in fold hinges producing crescent-shaped saddle-reef-like structures. Together these observations of truncation and replacement by dissolution and precipitation demonstrate that pressure solution and GBS facilitated both the formation of the phyllonitic shear zone and slip along it.

Connecticut↗