Rotationally-perturbed orbital elements of close binary systems

The aim of this investigation is to present the secular and periodic perturbations of the six orbital elements of a close binary system due to rotational distortion. In our study we consider very small inclinationst of the orbital plane of the system, whereas the eccentricity of the orbit may assume any value between 0<e<1. The final formulae for the various elements have been expressed by means of the unperturbed true anomaly measured from the ascending node.     

The fluvial and pyroclastic deposits of the Cagayan Basin, Northern Luzon, Philippines—an example of non-marine volcaniclastic sedimentation in an interarc basin

ABSTRACT The Cagayan basin of Northern Luzon, an interarc basin 250 km long and 80 km wide, contains a 900 m thick sequence of Plio-Pleistocene fluvial and pyroclastic deposits. These deposits are divided into two formations, the Ilagan and Awidon Mesa, and three lithofacies associations. The facies, which are interpreted as meandering stream, braided stream, lahar, and pyroclastic flow and fall deposits, occur in a coarsening upward sequence. Meandering stream deposits interbedded with tuffs are overlain by braided stream deposits interbedded with coarser pyroclastic deposits; lahars and ignimbrites. The coarsening upward volcaniclastic deposits reflect the tectonic and volcanic evolution of the adjacent Cordillera Central volcanic arc. Uplift of the arc resulted in the progradation of coarser clastics further into the basin, the development of an alluvial fan, and migration of the basin depocentre away from the arc. The coarsening of the pyroclastic deposits reflects the development of a more proximal calc-alkaline volcanic belt in the maturing volcanic arc. The Cagayan basin sediments serve as an example of the type and sequence of non marine volcaniclastic sediments that may form in other interarc basins. This is because the tectonic and volcanic processes which controlled sedimentation in the Cagayan basin also affect other arc systems and will therefore control or significantly influence volcaniclastic sedimentation in other interarc basins.     

Fumarolic gases at Mombacho volcano (Nicaragua): presence of magmatic gas species and implications for volcanic surveillance

Mombacho is a deeply dissected volcano belonging to the Quaternary volcanic chain of Nicaragua. The southern, historic collapse crater (El Crater) currently hosts a fumarolic field with a maximum temperature of 121°C. Chemical and isotopic data from five gas-sampling field campaigns carried out in 2002, 2003 and 2005 highlight the presence of high-temperature gas components (e.g. SO₂, HCl and HF), which indicate a significant contribution of juvenile magmatic fluids to the hydrothermal system feeding the gas discharges. This is strongly supported by the mantle-derived helium and carbon isotopic signatures, although the latter is partly masked by either a sedimentary subduction-related or a shallow carbonate component. The observed chemical and isotopic composition of the Mombacho fluids seems to indicate that this volcanic system, although it has not experienced eruptive events during the last centuries, can be considered active and possibly dangerous, in agreement with the geophysical data recorded in the region. Systematic geochemical monitoring of the fumarolic gas discharges, coupled with a seismic and ground deformation network, is highly recommended in order to monitor a possible new eruptive phase.     

Crystal chemistry of merrillite from Martian meteorites: Mineralogical recorders of magmatic processes and planetary differentiation

Merrillite is a ubiquitous accessory phase in a variety of Martian meteorite lithologies. The Martian merrillites exhibit a positive correlation between Mg# and Na and a negative correlation between Mg# and both Mn and vacancies in the octahedral Na‐site. Their REE patterns are varied and range from LREE‐depleted to LREE‐enriched. The dominant cation substitutions in the Martian merrillites are Fe²⁺_{VI Mg‐site}?Mg²⁺_{VI Mg‐site} and Ca²⁺_{VI Na‐site} +  □_{VI Na‐site}?2Na⁺_{VI Na‐site}. The REE substitution into the 8‐fold coordinated Ca‐site is accommodated by the coupled substitution Ca_{VIII Ca‐site} + (Na)_{VI Na‐site} ?(Y³⁺ + REE³⁺)_{VIII Ca‐site} + □_{VI Na‐site}. The REE substitution is significantly more prevalent in lunar merrillite and can be used as a “fingerprint” to distinguish lunar from Martian meteorites. The substitution of OH^? (whitlockite) and/or F^? (bobdownsite) for O^2? on one of the phosphate tetrahedrons appears to be rather insignificant. The correlations among Na, Mg#, Mn, and Na‐site vacancies are linked to the premerrillite crystallization history of the melt and the crystal chemical behavior of the Mg‐ and Na‐sites. The former reflects the sequence and extent of plagioclase and pyroxene crystallization. The differences in REE pattern shapes among the merrillites reflect source regions for the Martian basalts and the shapes are not greatly perturbed by the crystallization history. The occurrence of merrillite does not imply low‐volatile component in the Martian magmas. However, the low whitlockite and bobdownsite contents suggest that these samples were not altered by hydrothermal fluids and therefore not reset owing to aqueous fluid interactions. Consequently, the young ages of the shergottites are probably true igneous crystallization ages.     

The Darasun gold deposit,Eastern Transbaikal region: Chemical composition,REE patterns,and stable carbon and oxygen isotopes of carbonates from ore veins

The chemistry, REE patterns, and carbon and oxygen isotopic compositions of carbonates from ore veins of the Darasun deposit are discussed. In addition to the earlier described siderite, calcite, and carbonates of the dolomite-ankerite series, kutnahorite is identified. The total REE content in Fe-Mg carbonates of the dolomite-ankerite series (2.8–73 ppm) is much lower than in later calcite (18–390 ppm). δ¹³C of Fe-Mg carbonates and calcite varies from +1.1 to −6.7‰ and from −0.9 to −4.9‰, respectively. δ¹⁸O of Fe-Mg carbonates and calcite varies from +17.6 to 3.6‰ and from +15.7 to −0.5‰, respectively. The REE sum and carbon and oxygen isotopic compositions reveal zonal distribution relative to the central granodiorite porphyry stock. The correlation between the carbon and oxygen isotopic compositions and REE sum reflects variations in the physicochemical formation conditions and composition of ore-forming fluid. The isotopic composition of fluid is calculated, and possible sources of its components are considered. Earlier established evidence for a magmatic source of ore-forming fluid and participation of meteoric water in ore formation is confirmed. Geochemical evidence for interaction of ore-forming fluid with host rocks is furnished. The relationships between the REE sum, on the one hand, and carbon and oxygen isotopic compositions of hydrothermal ore-forming fluid, on the other, are established.     

Thermodynamic study of calcic amphiboles

The paper reports original thermochemical data on six natural amphibole samples of different composition. The data were obtained by high-temperature melt solution calorimetry in a Tian–Calvet microcalorometer and include the enthalpies of formation from elements for actinolite Ca_1.95(Mg_4.4Fe _0.5 ²⁺ Al₀₁)[Si_8.0O₂₂](OH)₂(–12024 ± 13 kJ/mol) and Ca_2.0(Mg_2.9Fe _1.9 ²⁺ Fe _0.2 ³⁺ )[Si_7.8Al_0.2O₂₂](OH)₂, (–11462 ± 18 kJ/mol), and Na_0.1Ca_2.0(Mg_3.2Fe _1.6 ²⁺ Fe _0.2 ³⁺ )[Si_7.7Al_0.3O₂₂](OH)₂ (–11588 ± 14 kJ/mol); for pargasite Na_0.5K_0.5Ca_2.0-(Mg_3.4Fe _1.8 ²⁺ Al_0.8)[Si_6.2Al_1.8O₂₂](OH)₂ (–12316 ± 10 kJ/mol) and Na_0.8K_0.2Ca_2.0(Mg_2.8Fe _1.3 ³⁺ Al_0.9) [Si_6.1Al_1.9O₂₂](OH)₂ (–12 223 ± 9 kJ/mol); and for hastingsite Na_0.3K_0.2Ca_2.0(Mg_0.4Fe _1.3 ²⁺ Fe _0.9 ³⁺ Al_0.2) [Si_6.4Al_1.6O₂₂](OH)₂ (?10909 ± 11 kJ/mol). The standard entropy, enthalpy, and Gibbs free energy of formation are estimated for amphiboles of theoretical composition: end members and intermediate members of the isomorphic series tremolite–ferroactinolite, edenite–ferroedenite, pargasite–ferropargasite, and hastingsite.     

Staurolite as an isotopic U–Pb geochronometer

A new approach is suggested for measuring the real U–Pb and Pb–Pb ages of rock-forming metamorphic staurolite. Previously, two approaches have been used for this purpose: (1) measurement of the lead isotopic compositions, uranium and lead contents in leach substance as a product of the step-leaching technique; age is calculated by plotting the Pb–Pb leaching isochron; and (2) lead and uranium isotopic compositions are measured in completely dissolved mineral material without leaching. In both cases, it is assumed a priori that inclusions, overgrowths, secondary phases, and the host mineral are cogenetic. This assumption may lead to errors in the measured age. The technique suggested in this paper uses various reagents (acids) to purify staurolite from the above-mentioned secondary phases while obtaining a staurolite “pure culture,” its subsequent disolution, introduction of the mixed spike, separation of lead and uranium compounds, and, finally, estimation of a real staurolite age using several samples to plot the monomineralic Pb–Pb isochron or by plotting measured Pb/U ratios in the diagram with concordia. The data can be used then to reconstruct the P–T–t evolution of metamorphism.     

Comet assay in phytoplankton as biomarker of genotoxic effects of environmental pollution

The alkaline comet assay was tested on different microalgae: the dinoflagellates, Karenia mikimotoi and Alexandrium minutum, and the diatom, Chaetoceros gracilis. The microalgae were exposed during their exponential growth to the model direct genotoxicant, hydrogen peroxide (1h, 5 and 100muM H2O2). Following H2O2 exposure, the comet assay was validated only for K. mikimotoi for which genotoxicity was observed from the lowest tested concentration of 5 microM with a concentration-dependent effect. C. gracilis was too small in size (4 microm) to be correctly analysed. For A. minutum, our lysis buffer was not strong enough to digest the cellulosic thecal plates. For K. mikimotoi, the comet assay was thus applied for the study of the genotoxic effects of different pesticides: epoxiconazole (as Opus formulation), chlorpyriphos-ethyl (as Dursban formulation) and endosulfan at 1, 10 and 100 microg of active substance/L for 24h. Exposure to epoxiconazole in formulation resulted in an increase in the extent of DNA strand breaks at the highest tested concentration icro/L. Endosulfan exposure resulted in DNA damage for K. mikimotoi nuclei. Genotoxicity was observed from 1 microg/L of endosulfan and was not concentration dependent.