Interpretation of neovolcanic versus palaeovolcanic sand grains: an example from Miocene deep-marine sandstone of the Topanga Group (Southern California)

Despite abundant data on volcaniclastic sand(stone), the compositional, spatial and temporal distribution of volcanic detritus within the sedimentary record is poorly documented. One of the most intricate tasks in optical analysis of sand(stone) containing volcanic particles is to distinguish grains derived by erosion of ancient volcanic rocks (i.e. palaeovolcanic, noncoeval grains) from grains generated by active volcanism (subaqueous and/or subaerial) during sedimentation (neovolcanic, coeval grains). Deep-marine volcaniclastic sandstones of the Middle Topanga Group of southern California are interstratified with 3000-m-thick volcanic deposits (both subaqueous and subaerial lava and pyroclastic rocks, ranging from basalt, andesite to dacite). These rocks overlie quartzofeldspathic sandstones (petrofacies 1) of the Lower Topanga Group, derived from deep erosion of a Mesozoic magmatic arc. Changes in sandstone composition in the Middle Topanga Group provide an example of the influence of coeval volcanism on deep-marine sedimentation. Volcaniclastic strata were deposited in deep-marine portions of a turbidite complex (volcaniclastic apron) built onto a succession of intrabasinal lava flows and on the steep flanks of subaerially emplaced lava flows and pyroclastic rocks. The Middle Topanga Group sandstones are vertically organized into four distinctive petrofacies (2–5). Directly overlying basalt and basaltic-andesite lava flows, petrofacies 2 is a pure volcanolithic sandstone, including vitric, microlitic and lathwork volcanic grains, and neovolcanic crystals (plagioclase, pyroxene and olivine). The abundance of quenched glass (palagonite) fragments suggests a subaqueous neovolcanic provenance, whereas sandstones including andesite and minor basalt grains suggest subaerial neovolcanic provenance. This petrofacies probably was deposited during syneruptive Periods, testifying to provenance from both intrabasinal and extrabasinal volcanic events. Deposited during intereruptive periods, impure volcanolithic petrofacies 3 includes both neovolcanic (85%) and older detritus derived from plutonic, metamorphic and palaeovolcanic rocks. During post-eruptive periods, the overlying quartzofeldspathic petrofacies 4 and 5 testify to progressive decrease of neovolcanic detritus (48–14%) and increase of plutonic-metamorphic and palaeovolcanic detritus. The Upper Topanga Group (Calabasas Formation), conformably overlying the Middle unit, has dominantly plutoniclastic sandstone (petrofacies 6). Neovolcanic detritus is drastically reduced (4%) whereas palaeovolcanic detritus is similar to percentages of the Lower Topanga Group (petrofacies 1). In general, the volcaniclastic contribution represents a well-defined marker in the sedimentary record. Detailed compositional study of volcaniclastic strata and volcanic particles (including both compositional and textural attributes) provides important constraints on deciphering spatial (extrabasinal vs. intrabasinal) and temporal relationships between neovolcanic events (pre-, syn-, inter- and post-eruptive periods) and older detritus.     

The Kovdor apatite-francolite deposit as a prospective source of phosphate ore

The mineral and chemical composition of phosphate ore, its texture and structure, and the distribution of trace elements are considered based on the results of geological exploration of the Kovdor apatitefrancolite deposit carried out in 2010–2012. The compositions of major, minor, and accessory minerals are reported. The ore varieties are typified depending on their composition, quality, texture, structure, and concentrating ability. The apatite-francolite ore occupies a certain position in the lateritic profile of carbonatite weathering and is of residual-infiltration origin as a zone of secondary phosphate enrichment. The outlook of the Kovdor deposit for this type of ore as a whole is considered in the context of phosphorus ore potential enhancement.     

Zircons,age, and geological setting of rhyodacite–porphyry from the Bagrusha Complex (South Urals)

Before our studies, it was considered that the Bagrusha rhyolite–porphyry complex (BC) including veins and thin dykes occurring in the Kusa region among deposits presumably of the Satka and Avzyan Formations of the Lower and Middle Riphean, respectively. Based on the U–Pb SHRIMP and IDTIMS studies of zircons from rhyodacite—porphyry, we established the age of the BC formation of T₀ = 1348.6 ± 3.2 Ma for the first time. The age obtained is inconsistent with the idea on the Paleozoic age of the BC and the geological situation shown on geological maps of the region. The age (T₀ = 1348.6 ± 3.2 Ma) of rhyodacite–porphyry from the BC provides evidence for acid volcanism controlled by the Mashak (Middle Riphean) magmatic event in the region, and deposits hosting volcanic rocks of the BC cannot be younger than the base of the Middle Riphean, i.e., the Mashak Formation, which was not previously distinguished by researchers in the western part of the Kusa and Bakal–Satka regions. At the same time, it is possible that deposits hosting dykes and veins of the granite–rhyolite formation may have a Bakal (Lower Riphean) age.     

The Timescales of Magma Mixing in the Plumbing System of Bezymianny Volcano (Kamchatka): Insights from Diffusion Chronometry

Intrusion of magma of contrasting composition into a magma chamber often triggers eruptions of arc volcanoes. Application of the diffusion chronometry method allowed us to determine the time when fresh magma was supplied to the shallow chamber of Bezymianny volcano in the case of six eruptions in 2006–2012 and to compare them to the recorded seismic activity of this volcano. Two types of eruptions of Bezymianny volcano were distinguished, with a contrasting orthopyroxene rim being formed in the respective magmas (a) up to 3 years and (b) up to 2 months before the beginning of an eruption. It was shown that these differences are caused by two different paths of magma supply to the shallow chamber of Bezymianny volcano.     

Geology and petrology of the lava complex of Young Shiveluch Volcano, Kamchatka

Detailed geological and petrological-geochemical study of rocks of the lava complex of Young Shiveluch volcano made it possible to evaluate the lava volumes, the relative sequence in which the volcanic edifice was formed, and the minimum age of the onset of eruptive activity. The lavas of Young Shiveluch are predominantly magnesian andesites and basaltic andesites of a mildly potassic calc-alkaline series (SiO₂ = 55.0–63.5 wt %, Mg# = 55.5–68.9). Geologic relations and data on the mineralogy and geochemistry of rocks composing the lava complex led us to conclude that the magnesian andesites of Young Shiveluch volcano are of hybrid genesis and are a mixture of silicic derivatives and a highly magnesian magma that was periodically replenished in the shallow-depth magmatic chamber. The fractional crystallization of plagioclase and hornblende at the incomplete segregation of plagioclase crystals from the fractionating magmas resulted in adakitic geochemical parameters (Sr/Y = 50–71, Y < 18 ppm) of the most evolved rock varieties. Our results explain the genesis of the rock series of Young Shiveluch volcano without invoking a model of the melting of the subducting Pacific slab at its edge.     

Zoning of diamonds from the Mir kimberlite pipe: Results of Fourier-transformed infrared spectroscopy

Plates prepared of diamonds from the Mir kimberlite pipe were examined with FTIR spectroscopy. It is shown that B1 defects were formed by annealing during crystal growth, whereas B2 centers arose after growth cessation. The development of B2 centers in a natural diamond is the secondary process with respect to the aggregation of the nitrogen admixture. The kinetics of this process is related to the breakdown of an oversaturated solid solution. The results obtained make it possible to estimate the temperature and duration of natural diamond growth.     

Atomistic computer modeling of the local structure and mixing properties of a grossular-uvarovite solid solution

An original methodology for the atomistic computer modeling of solid solutions was applied for the study of the mixing properties and local structure of the grossular-uvarovite, i.e., Ca₃Al₂[SiO₄]₃ Ca₃Cr₂][SiO₄]₃, garnet series. The parameters of the interatomic potentials for end members of this series were optimized using experimental data on their structural, elastic, and thermodynamic characteristics. The optimized model of the potentials allowed us to describe the elastic, structural, and thermodynamic characteristics of grossular and uvarovite and estimate the energy of point defects in these crystal structures. Calculations of the mixing properties and local structure for seven different compositions of the solid solution were carried out on a “Chebyshev” supercomputer (Moscow State University) in a 2 × 2 × 4 supercell of the garnet-type structure containing 2560 atoms. Mixing properties, such as the enthalpy of mixing, parameters of interaction, excess mixing volume, deviation of bulk modulus from additivity, and the vibrational and configuration contribution to the entropy of mixing, were determined. This allowed us to estimate the stability field for the grossular-uvarovite solid solution. Histograms of the interatomic distances M-O (M = Ca, Al, Cr, Si) and O-O in supercells were plotted and the parameters of relaxation and changes of the CrO₆ and AlO₆ octahedron volumes were estimated. The data of the simulation are quite consistent with the experimental data on this system and supplement it significantly.     

Mineralogy of morphogenetic types of ferromanganese deposits in the world ocean

The mineralogy and structural features of the main types of ferromanganese deposits—nodules, micronodules, Co-bearing crusts, crustlike nodules, and low-temperature hydrothermal manganese crusts and ferruginous ochers—are considered. The correlation between their mineral composition and structure is shown. The proposed classification of mineral types is based on characteristic assemblages of Fe and Mn minerals.     

Sr isotopic composition of Paleoproterozoic C-rich carbonate rocks: The Tulomozero Formation,SE Fennoscandian Shield

Rb–Sr systematics has been studied in ¹³C-rich carbonate rocks of the Paleoproterozoic (2.09 ± 0.07 Ga) Tulomozero Formation in the northern Onega Lake area, the SE Fennoscandian Shield. The formation is divided into eight members (A–F) consisting of greenschist-facies-grade, variegated sandstones, siltstones, mudstones, stromatolitic dolostones and subordinate crystalline limestones. Samples of carbonate rocks were obtained from two overlapping drillholes intersecting the entire thickness of the Tulomozero Formation. Prior to isotope analysis, the rocks powders were treated with 1N ammonium acetate for partial removal of the late epigenetic carbonate phases. Major resetting of the Rb–Sr systems in the Tulomozero carbonate rocks appears to take place during the Svecofennian regional metamorphic event, and it was screened by using Mn/Sr, Fe/Sr, Mg/Ca, and ¹⁸O/¹⁶O ratios. High Sr content (up to 2080 μg/g in limestones, and 530 μg/g in dolostones) coupled with low Fe/Mn (<0.40) ratios in the Tulomozero carbonate rocks of Members A, B (the lower part), D, F, and E are consistent with accumulation of original carbonate sediments in evaporitic lacustrine, playa, and sabkha environments. A decrease in the Sr content with concurrent increase in the Fe/Mn ratio (>0.40) in dolostones of the upper part of Member B, and of Members G and H is indicative of seawater influxes (sea transgression) into the Tulomozero basin. The ⁸⁷Sr/⁸⁶Sr values in the least altered (Mn/Sr < 2.0) marine dolostones are 0.70418–0.70442 and 0.70343–0.70409 for the earlier and late phases of the marine transgression, respectively. The decrease in the ⁸⁷Sr/⁸⁶Sr ratio in ca. 2.1 Ga seawater is attributable to an increase in hydrothermal flux Sr into the Palaeoproterozoic ocean.     

Crystal size distribution (CSD) in rocks and the kinetics and dynamics of crystallization

Crystal size distributions (CSDs) measured in metamorphic rocks yield quantitative information about crystal nucleation and growth rates, growth times, and the degree of overstepping (T) of reactions during metamorphism. CSDs are described through use of a population density function n=dN/dL, where N is the cumulative number of crystals per unit volume and L is a linear crystal size. Plots of ln (n) vs. L for olivine+pyroxene and magnetite in high-temperature (1000° C) basalt hornfelses from the Isle of Skye define linear arrays, indicating continuous nucleation and growth of crystals during metamorphism. Using the slope and intercept of these linear plots in conjunction with growth rate estimates we infer minimum mineral growth times of less than 100 years at T<10° C, and nucleation rates between 10^–4 and 10^–1/cm³/s. Garnet and magnetite in regionally metamorphosed pelitic schists from south-central Maine have CSDs which are bell-shaped. We interpret this form to be the result of two processes: 1) initial continuous nucleation and growth of crystals, and 2) later loss of small crystals due to annealing. The large crystals in regional metamorphic rocks retain the original size frequency distribution and may be used to obtain quantitative information on the original conditions of crystal nucleation and growth. The extent of annealing increases with increasing metamorphic grade and could be used to estimate the duration of annealing conditions if the value of a rate constant were known. Finally, the different forms of crystal size distributions directly reflect differences in the thermal histories of regional vs. contact metamorphosed rocks: because contact metamorphism involves high temperatures for short durations, resulting CSDs are linear and unaffected by annealing, similar to those produced by crystallization from a melt; because regional metamorphism involves prolonged cooling from high temperatures, primary linear CSDs are later modified by annealing to bell shapes.