USGS Science⌕ Search

SEARCH · USGS Science

Results for “Petrology”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,045 records · Page 58Linked to original sources

Pre-eruptive magmatic conditions at Augustine Volcano, Alaska, 2006: Evidence from amphibole geochemistry and textures

Variations in the geochemistry and texture of amphibole phenocrysts erupted from Augustine Volcano in 2006 provide new insights into pre- and syn-eruptive magma storage and mixing. Amphiboles are rare but present in all magma compositions (low- to high-silica andesites) from the 3 month long eruption. Unzoned magnesiohornblende in the high- and low-silica andesites exhibit limited compositional variability, relatively high SiO 2 (up to 49·7 wt %), and relatively low Al 2 O 3 (< 11·1 wt %). Intermediate-silica andesites and quenched mafic enclaves contain amphiboles that vary in composition (e.g. SiO 2 40·8–48·9 wt %, Al 2 O 3 6·52–15·2 wt %) and classification (magnesiohornblende–magnesiohastingsite–tschermakite). Compositional variation in amphibole is primarily controlled by temperature-dependent substitutions. Both high- and low-silica andesites represent remnant magmas that were stored in the shallow crust at 4–8 km depth, remaining distinct owing to a complex subsurface plumbing system. Intermediate-silica andesites and quenched mafic inclusions represent pre-eruptive hybrids of resident high- and low-silica andesite magmas and an intruding basalt. Amphiboles in explosive phase high-silica andesites are largely euhedral and unreacted, consistent with the high magma flux rates from depth during this phase (up to 13 800 m 3 s –1 ). Phenocrysts from the other lithologies have reaction rims that range from 1 to >1000 μm in thickness. Reaction rim microlite sizes correlate with reaction rim thicknesses. Reaction rims <50 μm thick contain microlites 1–10 μm in length whereas reaction rims >80 μm thick contain microlites 10–100 μm in length. Differentiating between heating- and decompression-induced amphibole reaction rim formation is problematic because of a lack of experimental constraints. We attempt a new approach to assessing reaction rim formation, based on a kinetic theory of crystal nucleation and growth, in which the differences in reaction rim textures represent different degrees of amphibole disequilibrium. Large crystals and low number densities suggest relatively lower levels of disequilibrium resulting in growth-dominated crystallization. Smaller crystals and larger number densities are indicative of higher nucleation rates and a high driving force.

Alaska↗

Pre-eruptive conditions of the Hideaway Park topaz rhyolite: Insights into metal source and evolution of magma parental to the Henderson porphyry molybdenum deposit, Colorado

The Hideaway Park tuff is the only preserved extrusive volcanic unit related to the Red Mountain intrusive complex, which produced the world-class Henderson porphyry Mo deposit. Located within the Colorado Mineral Belt, USA, Henderson is the second largest Climax-type Mo deposit in the world, and is therefore an excellent location to investigate magmatic processes leading to Climax-type Mo mineralization. We combine an extensive dataset of major element, volatile, and trace element abundances in quartz-hosted melt inclusions and pumice matrix glass with major element geochemistry from phenocrysts to reconstruct the pre-eruptive conditions and the source and evolution of metals within the magma. Melt inclusions are slightly peraluminous topaz rhyolitic in composition and are volatile-charged (&le;6&thinsp;wt % H 2 O, &le;600&thinsp;ppm CO 2 , &sim;0&middot;3&ndash;1&middot;0&thinsp;wt % F, &sim;2300&ndash;3500&thinsp;ppm Cl) and metal-rich (&sim;7&ndash;24&thinsp;ppm Mo, &sim;4&ndash;14&thinsp;ppm W, &sim;21&ndash;52&thinsp;ppm Pb, &sim;28&ndash;2700&thinsp;ppm Zn, <0&middot;1&ndash;29&thinsp;ppm Cu, &sim;0&middot;3&ndash;1&middot;8&thinsp;ppm Bi, &sim;40&ndash;760&thinsp;ppb Ag, &sim;690&ndash;1400&thinsp;ppm Mn). Melt inclusion and pumice matrix glass chemistry reveal that the Hideaway Park magma evolved by large degrees of fractional crystallization (&le;60&ndash;70%) during quartz crystallization and melt inclusion entrapment at pressures of &le;300&thinsp;MPa (&le;8&thinsp;km depth), with little to no crystallization upon shallow ascent and eruption. Filter pressing, crystal settling, magma recharge and mixing of less evolved rhyolite melt, and volatile exsolution were important processes during magma evolution; the low estimated viscosities (&sim;10 5 &ndash;10 10&thinsp; Pa s) of these H 2 O- and F-rich melts probably enhanced these processes. A noteworthy discrepancy between the metal contents in the pumice matrix glass and in the melt inclusions suggests that after quartz crystallization ceased upon shallow magma ascent and eruption, the Hideaway Park magma exsolved an aqueous fluid into which Mo, Bi, Ag, Zn, Mn, Cs, and Y strongly partitioned. Given that the Henderson deposit contains anomalous abundances of not only Mo, but also W, Pb, Zn, Cu, Bi, Ag, and Mn, we suggest that these metals were sourced from similar fluids exsolved from unerupted portions of the same magmatic system. Trace element ratios imply that Mo was sourced deep, from either the lower crust or metasomatized mantle. The origin of sulfur remains unresolved; however, given the extremely low S solubility of rhyolite melts in the shallow crust we favor the possibility that another source of S might supplement or account for that present in the ore deposit, probably the comagmatic, mantle-derived lamprophyres that occur in minor quantities with the voluminous topaz rhyolites in the area. To account for the 437&thinsp;Mt of MoS 2 (&sim;1&middot;0&thinsp;&times;&thinsp;10 6&thinsp; t Mo) present in the Henderson ore deposit, a volume of &sim;45&thinsp;km 3 of Hideaway Park rhyolite magma would have been necessary to supply the Mo (a cylindrical pluton measuring 3&middot;1&thinsp;km&thinsp;&times;&thinsp;6&middot;0&thinsp;km) along with sparging of &sim;6&middot;8&thinsp;&times;&thinsp;10 5&thinsp; t of S from &sim;0&middot;05&thinsp;km 3 of lamprophyre magma. Based on a weighted mean 40 Ar/ 39 Ar age of 27&middot;58&thinsp;&plusmn;&thinsp;0&middot;24&thinsp;Ma, similar melt geochemistry, and characteristically F-rich biotite phenocrysts, we conclude that the Hideaway Park tuff was cogenetic with the intrusions at Red Mountain that formed the Henderson deposit.

Colorado↗

Mechanisms and timescales of generating eruptible rhyolitic magmas at Yellowstone caldera from zircon and sanidine geochronology and geochemistry

We constrain the physical nature of the magma reservoir and the mechanisms of rhyolite generation at Yellowstone caldera via detailed characterization of zircon and sanidine crystals hosted in three rhyolites erupted during the (ca. 170 &ndash; 70 ka) Central Plateau Member eruptive episode &ndash; the most recent post-caldera magmatism at Yellowstone. We present 238U-230Th crystallization ages and trace-element compositions of the interiors and surfaces (i.e., unpolished rims) of individual zircon crystals from each rhyolite. We compare these zircon data to 238U- 230Th crystallization ages of bulk sanidine separates coupled with chemical and isotopic data from single sanidine crystals. Zircon age and trace-element data demonstrate that the magma reservoir that sourced the Central Plateau Member rhyolites was long-lived (150 &ndash; 250 kyr) and genetically related to the preceding episode of magmatism, which occurred ca. 256 ka. The interiors of most zircons in each rhyolite were inherited from unerupted material related to older stages of Central Plateau Member magmatism or the preceding late Upper Basin Member magmatism (i.e., are antecrysts). Conversely, most zircon surfaces crystallized near the time of eruption from their host liquids (i.e., are autocrystic). The repeated recycling of zircon interiors from older stages of magmatism demonstrates that sequentially erupted Central Plateau Member rhyolites are genetically related. Sanidine separates from each rhyolite yield 238U-230Th crystallization ages at or near the eruption age of their host magmas, coeval with the coexisting zircon surfaces, but are younger than the coexisting zircon interiors. Chemical and isotopic data from single sanidine crystals demonstrate that the sanidines in each rhyolite are in equilibrium with their host melts, which considered along with their near-eruption crystallization ages suggests that nearly all CPM sanidines are autocrystic. The paucity of antecrystic sanidine crystals relative to antecrystic zircons require a model where eruptible rhyolites are generated by extracting melt and zircons from a long-lived mush of immobile crystal-rich magma. In this process the larger sanidine crystals remain trapped in the locked crystal network. The extracted melts (plus antecrystic zircon) amalgamate into a liquid dominated (i.e., eruptible) magma body that is maintained as a physically distinct entity relative to the bulk of the long-lived crystal mush. Zircon surfaces and sanidines in each rhyolite crystallize after melt extraction/amalgamation and their ages constrain the residence time of eruptible magmas at Yellowstone. Residence times of the large volume rhyolites (~40 &ndash; 70 km3) are &le; 1 kyr (conservatively < 6 kyr), which suggests that large volumes of rhyolite can be generated rapidly by extracting melt from a crystal mush. Because the lifespan of the crystal mush that sourced the Central Plateau Member rhyolites is two orders of magnitude longer than the residence time of eruptible magma bodies within the reservoir, it is apparent that the Yellowstone magma reservoir spends most of its time in a largely-crystalline (i.e., uneruptible) state, similar to the present-day magma reservoir, and that eruptible magma bodies are ephemeral features.

Idaho, Wyoming↗

238U–230Th–226Ra–210Pb–210Po disequilibria constraints on magma generation, ascent, and degassing during the ongoing eruption of Kīlauea

The timescales of magma genesis, ascent, storage and degassing at Kīlauea volcano, Hawai‘i are addressed by measuring 238 U-series radionuclide abundances in lava and tephra erupted between 1982 and 2008. Most analyzed samples represent lavas erupted by steady effusion from Pu‘u ‘Ō‘ō and Kūpahianaha from 1983 to 2008. Also included are samples erupted at the summit in April 1982 and March 2008, along the East Rift Zone at the onset of the ongoing eruption in January 1983, and during vent shifting episodes 54 and 56, at Nāpau crater in January 1997, and Kane Nui O Hamo in June 2007. In general, samples have small (∼4%) excesses of ( 230 Th) over ( 238 U) and ∼3 to ∼17% excesses of ( 226 Ra) over ( 230 Th), consistent with melting of a garnet peridotite source at melting rates between 1 × 10 –3 and 5 × 10 –3 kg m –3 a –1 , and melting region porosity between ∼2 and ∼10%, in agreement with previous studies of the ongoing eruption and historical eruptions. A small subset of samples has near-equilibrium ( 230 Th/ 238 U) values, and thus were generated at higher melting rates. Based on U–Th–Ra disequilibria and Th isotopic data from this and earlier studies, melting processes and sources have been relatively stable over at least the past two centuries or more, including during the ongoing unusually long (>30 years) and voluminous (4 km 3 ) eruption. Lavas recently erupted from the East Rift Zone have average initial ( 210 Pb/ 226 Ra) values of 0·80 ± 0·11 (1σ), which we interpret to be the result of partitioning of 222 Rn into a persistently generated CO 2 -rich gas phase over a minimum of 8 years. This ( 210 Pb) deficit implies an average magma ascent rate of ≤3·7 km a –1 from ∼30 km depth to the surface. Spatter and lava associated with vent-opening episodes erupt with variable ( 210 Pb) deficits ranging from 0·7 to near-equilibrium values in some samples. The samples with near-equilibrium ( 210 Pb/ 226 Ra) are typically more differentiated, suggesting decadal timescales of magma storage in shallow conduits or reservoirs that were not degassing. Lava and spatter samples erupted in the East Rift Zone and at the summit had ( 210 Po) ∼0 at the time of eruption, which results from efficient partitioning of Po into the CO 2 - and SO 2 -rich gas phases during and prior to eruption. Summit ash and Pele’s hair samples from 2008 differ from lava and lapilli samples in that they have elevated initial ( 210 Po), ( 210 Pb/ 226 Ra), and Pb concentrations because of Po condensation on tephra particles, and incorporation of fumarolic Po and Pb into erupted tephra fragments during quenching.

Hawaii↗

Caldera life-cycles of the Yellowstone hotspot track: Death and rebirth of the Heise Caldera

As one of the most geochemically unique drill cores recovered within the Yellowstone–Snake River Plain (YSRP) province, the Sugar City geothermal test well was drilled into intra-caldera rhyolite lavas and tuffs erupted during the middle to late Pliocene and the resurgent basaltic volcanism erupted during the Pleistocene. This sequence parallels the two main stages proposed for YSRP hotspot calderas: i.e. the eruption of several large-volume, ash-flow tuff sheets followed by caldera collapse, then cessation of major rhyolitic activity and gradual subsidence accompanied by filling and eventual burial of the caldera by basalt lava flows. We employ stratigraphic relationships, paleomagnetism, and major, trace element, and Sr–Nd isotope geochemistry to develop models for the origin of the basaltic and rhyolitic magmas within a geographical and temporal context. The basalts are characterized by distinct groupings based on depth and geochemistry and reflect the dominant compositions observed on the surface, e.g. Snake River olivine tholeiite (SROT) and evolved type (e.g. Craters of the Moon). We also observe contaminated basalts that interacted with rhyolite/granite. The basaltic magma formed by shallow partial melting in the plume channel carved into the lithosphere. The older rhyolites preserve the classical characteristics of A-type granites and display major element and trace element concentrations typical for Eastern SRP caldera centres and minimal stratigraphic variation. Multiple lines of evidence document extensive magmatic differentiation and coupled basalt–rhyolite interactions. We find that the most plausible origin for the rhyolites is via partial melting of a hybrid source, comprising Archean crustal components and younger juvenile mafic intrusions. Assimilation of hydrothermally altered material is also required for some eruptive units. The rhyolites did not evolve from residual magma left over from the climactic Kilgore eruption (4·0 Ma), but instead represent discrete magma generation events in the course of a few hundred thousand years between 4·0 to 3·8 Ma. Beginning at approximately 3.3 Ma, basalts were able to erupt through the solidified composite pluton that formed below the caldera. The transition from rhyolite to basalt is tied to the declining flux of basaltic magma as North America moved away from the Yellowstone hotspot core.

Journal of Petrology↗

Intrinsic Nd, Pb, and Sr isotopic heterogeneities exhibited by the Lherz Alpine Peridotite Massif, French Pyrenees

Optically clear, acid-leached Cr-diopside, Al-augite, pargasitic amphibole, and phlogopite from peridotite and ultramafic dikes of the Lherz massif (French Pyrenees) exhibit chemical and isotopic heterogeneities indicative of a complex history. The data cover a wide range on the 143 Nd/ 144 Nd vs. 87 Sr/ 86 Sr covariation diagram, encompassing much of the mantle array and a large area below the array. Pb-isotopic signatures cover a wide range on Pb-Pb correlation diagrams, with several samples falling in the mid-ocean ridge basalt (MORB) field, but with others defining trends towards the enriched mantle II (EM II) and high-mu (HIMU) endmembers of Zindler & Hart (1986). Peridotites display the largest range in isotopic compositions, which formed in response to variable degrees of partial melting and subsequent enrichment during the intrusion of the ultramafic dikes. The ultra-mafic dikes represent at least four generations. Dike isotopic compositions range from ‘depleted’ to ‘enriched’, relative to Bulk Earth, reflecting the average composition of their source regions and subsequent melt-wall rock interactions. No simple isochronous relationships are observed on the 143 Nd/ 144 Nd vs. 147 Sm/ 144 Nd diagram for any lithologic group, demonstrating that the rock assemblages were not created by simple mixing of two homogeneous endmembers. Some ultramafic dikes, which represent low-temperature melt fractions, are enriched in the heavy isotopes of Sr, Nd, and Pb; any magmas derived from partial melting of these dikes are likely to have enriched isotopic signatures, particularly when the degrees of partial melting are only a few per cent.

Pyrenees↗

Factors controlling heavy-mineral variations on the South Texas outer continental shelf, Gulf of Mexico

Heavy-mineral distribution on the outer continental shelf off the southern coast of Texas shows regional variability induced by provenance and local variability reflecting genetic differences in sea-floor sediments. Q-mode factor analysis showed that three suites of heavy minerals are present. The southern ancestral Rio Grande delta sediments contain a distinct opaque-pyroxene-garnet suite, whereas the northern ancestral Brazes-Colorado delta sediments contain a tourmaline-green hornblende suite. An interdelta region contains a heavy mineral suite that is mixed owing to contributions from both ancestral deltas. Analysis of variance, correlation, and regression methods indicate that heavy-mineral variations in each sedimentary province have been significantly influenced by hydraulic fractionation by size, shape, and density, and by a selective chemical decomposition of unstable minerals. These factors have operated at varying degrees on the relict, palimpsest, and modern sediment populations of the sedimentary provinces since the end of Pleistocene time. The differential effects of these processes on the sediments have resulted in local variations that contribute to the total mineralogical variability. A comparison of the heavy mineral suites of the modern and relict Rio Grande delta sediments, which are derived from a common provenance, also shows mineral variations resulting from factors other than provenance.

Texas↗

Estimating pore and cement volumes in thin section

Point count estimates of pore, grain and cement volumes from thin sections are inaccurate, often by more than 100 percent, even though they may be surprisingly precise (reproducibility + or - 3 percent). Errors are produced by: 1) inclusion of submicroscopic pore space within solid volume and 2) edge effects caused by grain curvature within a 30-micron thick thin section. Submicroscopic porosity may be measured by various physical tests or may be visually estimated from scanning electron micrographs. Edge error takes the form of an envelope around grains and increases with decreasing grain size and sorting, increasing grain irregularity and tighter grain packing. Cements are greatly involved in edge error because of their position at grain peripheries and their generally small grain size. Edge error is minimized by methods which reduce the thickness of the sample viewed during point counting. Methods which effectively reduce thickness include use of ultra-thin thin sections or acetate peels, point counting in reflected light, or carefully focusing and counting on the upper surface of the thin section.

Journal of Sedimentary Petrology↗

Inverse grading and hydraulic equivalence in grain-flow deposits

Inversely graded grain-flow deposits are characterized by a hydraulic equivalence that differs from that based on settling velocities or entrainment. Dispersive equivalence, derived from the dispersive pressure hypothesis on how inverse grading develops, was found to agree reasonably well with observed relationships between grain sizes and densities in grain-flow deposits. Furthermore, observed relationships in deposits formed in subaerial and subaqueous environments were found to be independent of fluid density as is required by dispersive equivalence. The results suggest that dispersive pressure controls the development of the inverse grading common to beach foreshore laminations, slip-face foreset strata, the basal parts of some coarse-grained turbidites, and other diverse deposits.

Journal of Sedimentary Petrology↗

Fresh-water cementation of a 1,000-year-old oolite

Calcite cementation of aragonite ooid sand is producing oolite on Joulters Cays, Bahamas. During the last 1,000 years, calcite cement has formed at an average rate of between 27 and 55 cm 3 /m 3 /yr and is derived from dissolution of ooid aragonite in fresh water. The dissolution-reprecipitation of carbonate minerals in the aquifer results in ground waters of unusually high Sr content. Sea water and mixtures of fresh and sea water appear to inhibit cementation. A pronounced cement fabric change occurs across the water table and has produced an obvious petrographic record of fresh-water diagenesis. Above the water table, cement is typically near grain contact positions, where water is held by capillarity; below the water table, cement is more randomly distributed around grains. At the water table a transition zone, 1 meter thick, marks the boundary between cement textures. No porosity reduction is associated with cementation; calcite cement precipitation is apparently compensated by an equal or greater amount of aragonite dissolution in the interval undergoing cementation. Permeability is more variable above the water table than below it, reflecting early channelling of flow patterns in the vadose zone. Effective permeability below the water table is one to two orders of magnitude higher than above the water table because of entrained gas in the vadose zone. This permeability difference promotes preservation of unstable minerals above the water table and continued diagenetic alteration below the water table.

Joulters Cays↗

Comparison of bed form variance spectra within a meander bend during flood and average discharge

Time series analysis of streambed elevation in a meander bend along the Congaree River was used to determine the changes in bed form population succeeding a 16-year flood event. Bed forms observed during the flood event had a significantly greater total height variance than bed forms observed at the same location one week later. Variance spectra were computed for a 595 m longitudinal profile. The data indicate that: a) the bed form variance for the flood record is significantly greater for all wavelengths from 5 to 30 m; b) no well-demarcated bed form classes were present during the survey times, pointing to the possible existence of a continuum of bed form sizes rather than well-defined classes; and c) bed forms produced by the flood discharge were rapidly altered as the stage returned toward average level.

Journal of Sedimentary Petrology↗

Dissolution and analysis of amorphous silica in marine sediments

The analytical estimation of amorphous silica in selected Atlantic and Antarctic Ocean sediments, the U.S.G.S. standard marine mud (MAG-1), A.A.P.G. clays, and samples from cultures of a marine diatom, Hemidiscus, has been examined. Quantitative recovery of sedimentary amorphous silica was achieved by reacting 2 M Na 2 CO 3 with a sample for 4 hours at 90 degrees -100 degrees C; where necessary, aluminum analysis is used to correct for the extraction of non-amorphous silica. Oceanic sediments having an amorphous SiO 2 /clay ratio of 1.0 or more can be analyzed by a single extraction with 2 M Na 2 CO 3 , without correction for non-amorphous additions. Marine sediments having an amorphous SiO 2 /clay ratio of from 1.0 to 0.25 can be corrected for inputs of clay-derived silica using an aluminum determination and an empirical correction factor. Sediments with amorphous SiO 2 /clay ratios of less than 0.25, samples containing non-silica-bearing aluminous materials such as gibbsite, or materials having low absolute levels of amorphous silica require successive leaches to accurately correct for silica inputs from non-amorphous sources. Our values for amorphous silica-rich circum-Antarctic sediments are equal to or greater than literature values, whereas our values for a set of amorphous silica-poor sediments from a transect of the North Atlantic at 11 degrees N, after appropriate correction for silica released from clays, are significantly lower than previous estimates from the same region.

Journal of Sedimentary Petrology↗

The provenance of rutile.

Most coarse detrital rutile is derived from high-grade metamorphic rocks. Contrary to a conventional assumption, independent rutile grains are particularly rare in igneous rocks except alkalic rocks. The use of rutile in the ZTR (zircon-tourmaline-rutile) index of mineralogic maturity is only partially valid, owing to its restricted provenance.

Journal of Sedimentary Petrology↗

Opaque minerals as aids in distinguishing between source and sorting effects on beach sand mineralogy in southwestern Oregon

Both source area and wave sorting affect the heavy-mineral distributions of beach sands. Although source and sorting effects are difficult to distinguish, they can be separated on four Oregon beaches by studying the magnetic fraction of the sand. Prominent headlands bound the four beaches, which are located on the southwestern Oregon coast. On three beaches the percentage of magnetite in the sand from the upper swash zone consistently increases toward the north end of each beach, apparently owing to selective sorting during littoral transport. However, the percentages of chromium and titanium in the magnetite are generally independent of the relative location of the samples along the beach and therefore independent of sorting effects. Each beach appears to be characterized by a fairly distinct range of Ti/Cr in the magnetic fraction, and the range differs from beach to beach. The magnetite percentage and the Ti/Cr range suggest that sorting and source effects can be distinguished on beaches rich in "black" sands, and that sand transport around headlands in this area is not extensive enough to mask source differences. The results of this study suggest that sorting and source effects can be distinguished wherever there are chemical or mineralogical differences in a restricted density fraction.

Journal of Sedimentary Petrology↗

Paleoenvironment of the New Albany Shale Group ( Devonian- Mississippian) of Illinois

The distribution of lithofacies in the New Albany Shale Group of Illinois was determined by wave energy, bottom oxygenation, and bottom topography in a deep water stratified anoxic basin. A transect from the margin to the center of the Illinois Basin reveals a complete transition from high energy, aerobic, shallow-water environments to quiet, anaerobic, deep-water environments. Shallow areas at the margin of the basin are characterized by rapid facies transitions over short distances. High energy, very shallow conditions are recorded by oolitic-skeletal grainstones and packstones with abundant brachiopods, crinoids, trilobites, and other calcified marine invertebrates. Bioturbation did not destroy primary sedimentary structures in these facies. Offshore, less agitated areas are represented by highly bioturbated carbonate wackestones, argillaceous quartz siltstones, and greenish-gray mudstones. Calcified invertebrates are generally rare in these facies, indicating deposition in dysaerobic conditions. Basinward, slope areas are characterized by olive-gray to black, weakly bioturbated shales commonly interbedded with thickly laminated black shales. Trace fossils, including Zoophycos, Chondrites , and Planolites , are abundant along the bases of the olive-gray beds. In areas where the anaerobic/dysaerobic boundary intersected the bottom slope, slight fluctuations of the position of the boundary resulted in thin interbedding of olive-gray and black shales and laterally persistent interfingering of the two lithologies. Anaerobic conditions prevailed during most of New Albany time in the deepest areas of the basin, and finely laminated, undisturbed, pelagic black shales were deposited.

Journal of Sedimentary Petrology↗

Littoral transport in the surf zone elucidated by an Eulerian sediment tracer

An Eulerian, or time integration, sand tracer experiment was designed and carried out in the surf zone near Pt. Mugu, California on April 19, 1972. Data indicate that conditions of stationarity and finite boundaries required for proper application of Eulerian tracer theory exist for short time periods in the surf zone. Grain counts suggest time required for tracer sand to attain equilibrium concentration is on the order of 30-60 minutes. Grain counts also indicate transport (discharge) was strongly dependent upon grain size, with the maximum rate occurring in the size 2.5-2.75phi (0.18-0.15 mm) decreasing to both finer and coarser sizes. The measured instantaneous transport was at the annual rate of 2.4 x 10 6 m 3 /yr.

Journal of Sedimentary Petrology↗

Thickness change involved in the peat-to- coal transformation for a bituminous coal of Cretaceous age in central Utah

The ratio of the thicknesses of a layer of peat and the coal bed formed from that peat has been calculated for a bituminous coal bed in central Utah. The method used involves comparison of the thickness of peat eroded by a laterally migrating channel system with the thickness of coal now absent from the outcrop. The peat:coal thickness ratio calculated by this method is approximately 11:1.

Journal of Sedimentary Petrology↗