Carbon isotopic fractionation between CO2 vapour,silicate and carbonate melts: an experimental study to 30 kbar

The carbon isotopic fractionation between CO₂ vapour and sodamelilite (NaCaAlSi₂O₇) melt over a range of pressures and temperatures has been investigated using solid-media piston-cylinder high pressure apparatus. Ag₂C₂O₄ was the source of CO₂ and experimental oxygen fugacity was buffered at hematite-magnetite by the double capsule technique. The abundance and isotopic composition of carbon dissolved in sodamelilite (SM) glass were determined by stepped heating and the ¹³C of coexisting vapour was determined directly by capsule piercing. CO₂ solubility in SM displays a complex behavior with temperature. At pressures up to 10 kbars CO₂ dissolves in SM to form carbonate ion complexes and the solubility data suggest slight negative temperature dependence. Above 20 kbars CO₂ reacts with SM to form immiscible Na-rich silicate and Ca-rich carbonate melts and CO₂ solubility in Na-enriched silicate melt rises with increasing temperature above the liquidus. Measured values for carbon isotopic fractionation between CO₂ vapour and carbonate ions dissoived in sodamelilite melt at 1200°–1400° C and 5–30 kbars average 2.4±0.2, favouring¹³C enrichment in CO₂ vapour. The results are maxima and are independent of pressure and temperature. Similar values of 2 are obtained for the carbon isotopic fractionation between CO₂ vapour and carbonate melts at 1300°–1400° C and 20–30 kbars.     

Monazite U-Pb dating of staurolite grade metamorphism in pelitic schists

A study of the occurrence of and relations between rare-earth element (REE) minerals in pelitic schists indicates that monazite forms at or near the P and T of the staurolite isograd. Samples at staurolite grade from the Silurian Perry Mountain Formation in the Rumford quadrangle of Maine yield monazite in sufficient quantities to permit accurate dating of the metamorphic events forming the monazites. The bulk chemistry of the metapelites, as seen in the major element abundances and REE patterns, does not vary significantly across the study area. Thus the appearance and disappearance of REE phases is assumed to reflect changes in metamorphic grade. In a sample from the biotite zone, scanning electron microscope and microprobe studies show allanite and monazite intimately associated on a 10 m scale. The texture suggest that metastable detrital monazite breaks down, distributing its REE components to allanite. From samples below staurolite grade in which monazite is not present, our observations suggest that REEs are partitioned into allanite. At or near the staurolite isograd monazite forms as a metamorphic mineral, initiating its role as a geochronometer. Garnet-biotite geothermometry on samples at this grade from this and other studies places constraints on the minimum temperature necessary to form monazite: 525° C±25°C at 3.1±0.25 kbar. A total of 15 separates from nine schist samples ranging up to sillimanite grade have been dated. Each date is remarkably concordant, even though petrologic and textural studies by previous workers have shown that the rocks in the area have been affected by at least three metamorphic episodes. Calculations indicate insignificant Th disequilibrium in these monazites. The conditions associated with the metamorphic events suggest that monazite remains closed to lead loss provided that subsequent metamorphisms are at or below sillimanite grade. Two distinct metamorphic events are resolved, one at around 400 Ma and one at about 370 Ma. The latter was due to thermal effects of a nearby pluton that yields concordant monazite ages of 363 Ma. This work suggests that in addition to dating plutonism and high-grade metamorphism, monazite should be viewed as a reliable geochronometer for moderate metamorphism of pelitic schists.     

Geochemistry and Intrusive History of the Ashland Pluton, Klamath Mountains, California and Oregon

The Ashland pluton is a calc-alkaline plutonic complex thatintruded the western Paleozoic and Triassic belt of the KlamathMountains in late Middle Jurassic time. The pluton comprisesa series of compositionally distinct magma pulses. The oldestrocks are hornblende gabbro and two-pyroxene quartz gabbro withinitial ⁸⁷Sr/⁸⁶Sr = 0{dot}7044, ¹⁸O = 8{dot}7%, and REE patternswith chondrite normalized La/Lu = 7. These units were followedby a suite of tonalitic rocks (La_N/Lu_N = 7) and then by a suiteof K₂O- and P₂O₅ rocks of quartz monzodioritic affinity (La_N/Lu_N= 13–21; La_N/Sm_N = 2{dot}4–3{dot}) The quartz monzodioriticrocks were then intruded by biotite granodiorite and granitewith lower REE abundances but more fractionated LREE(La_N/Lu_N= 13–19; La_N/Sm_N = 4{dot}3–6 and they, in turn,were host to dikes and bosses of hornblende diorite. The latestintrusive activity consisted of aplitic and granitic dikes.Combined phase equilibria and mineral composition data, indicateemplacement conditions of approximately P_total = 2{dot}3kb,P_H2O between 1{dot}5 and 2{dot}2 kb, and f_O2 between the nickel-nickeloxide and hematite-magnetite buffers. Successive pulses of magma display increasing SiO₂ togetherwith increasing ¹⁸O and decreasing initial ⁸⁷Sr/⁸⁶Sr. The isotopicdata are consistent with either (1) combined fractional crystallizationof andesitic magma and concurrent assimilation of crustal materialcharacterized by low Sr₁ and high (¹⁸O or, more probably, (2)a series of partial melting events in which sources were successivelyless radiogenic but richer in ¹⁸O Each intrusive stage displaysevidence for some degree of crystal accumulation and/or fractionalcrystallization but neither process adequately accounts fortheir compositional differences. Consequently, each stage appearsto represent a distinct partial melting or assimilation event. The P₂O₅-rich nature of the quartz monzodiorite suite suggestsaccumulation of apatite. However, the suite contains abundantmafic microgranitoid enclaves and most apatite in the suiteis acicular. These observations suggest that magma mixing affectedthe compositional variation of the quartz monzodiorite suite.Mass balance calculations are consistent with a simple mixingprocess in which P₂O₅-rich alkalic basalt magma (representedby the mafic microgranitoid enclaves) was combined with a crystal-poorfelsic magma (represented by the tonalite suite), yielding aquartz monzodioritic magma that then underwent differentiationby crystal fractionation and accumulation.     

Interaction of S- and L-bursts in Jupiter's decametric radio spectra

Dynamic spectra of Jupiter's decametric emission are observed with a high-resolution radio spectrograph. Certain events observed in region Io-B display interaction effects between the S- and L-emissions. The effect appears as a gap in the L-emission after a passage of an S-burst. In a typical case the L-emission has a relatively narrow bandwidth, the S-burst appears as a sloping line crossing it, and the duration of the emission gap is a substantial fraction of a second. The gap has sharp, sloped edges; its leading edge has anf-t slope which is the same as that of the S-burst while the slope of the trailing edge is lower. A kind of tilted V-pattern is thus formed. It is suggested that some more complicated spectral patterns may also be produced this way. It seems that an emission model consisting of S-bursts from bunches of gyrofrequency-emitting electrons ascending a flux tube and interacting with L-emitting bunches of electrons having more stationary guiding centers is inadequate to explain the complex S-L interactions.Contribution of No. 36 of the Department of Astronomy, University of Florida, U.S.A.     

Earth-orbit-approaching comets and their theoretical meteor radiants

Sixteen comets produce recognizable meteor showers that are found in A. F. Cook's (1973, In Evolutionary and Physical Properties of Meteoroids (C. L. Hemenway, P. M. Millman, and A. F. Cook, Eds.), pp. 183–191, U.S. Govt. Printing Office, Washington, D.C.), working list of meteor streams. Of these, five are long period, including one in a parabolic and one in a hyperbolic orbit. The largest Earth-comet orbit miss distance is 0.20 AU for P/Encke and the Northern and Southern Taurids. Using this is an upper limit for meteor showers from comets, all comets which approach the Earth's orbit to within 0.20 AU were extracted from the Catalogue of Cometary Orbits (B. G. Marsden, 1979. 3rd ed., Central Bureau of Astronomical Telegrams, IAU SAO, Cambridge, Mass.). A compilation of such comets is presented by date minimum approach, along with the distance of closest approach and the theoretical geocentric radiants and velocities of possible associated meteor showers. Both pre- and postpperihelion encounters with the Earth's orbit are considered. There are 240 entries for 178 long-period comets, and 36 for 28 short-period comets. It is noted that all short-period comets that have approached the Earth's orbit to within 0.08 AU have produced meteors, except P/Lexell, P/Finlay, P/Denning-Fujikawa, and P/Grigg-Skjellerup. Attention is called to the favorable observing conditions for detecting meteors from P/Grigg-Skjellerup in April 1982, and for the possibility of another great Draconid storm from P/Giacobini-Zinner in October 1985. A comparison is made between observed sporadic meteor rates and the distribution of theoretical radiants throughout the year, from which it is concluded that the currently known comets can account for sporadic meteors. A criterion is developed to test whether or not an observed meteor shower can be associated with a given theoretical radiant. Based on known examples, a qualitative model for comet/meteor relationships is also presented.     

On periodic flybys of the moon

This paper considers the plane circular restricted three-body problem for small . Symmetric periodic solutions of the second species (passing near the body of mass ) and their distance from the center of the body of mass are studied by constructing perturbations of arc-solutions (solutions with consecutive collisions) existing for =0. Orbits which also pass near the body of mass 1- are studied in detail. The results are applied to finding periodic orbits in the Earth-Moon system and in the Sun-Jupiter system.Russian version: Preprint No. 91 (1978) of Inst. Appl. Math.; present English translation was made by L. M. Perko and W. C. Schulz (February 1979).     

Hydrocarbons in surficial sediments from the Scotian Shelf

Surface sediments from 20 stations on the Scotian Shelf, collected on a transect from Halifax to Emerald Bank and around Sable Island, have been analyzed for hydrocarbon content and composition by gas chromatography and fluorescence spectrophotometry. Some samples were taken near abandoned exploratory drilling sites in the Sable Island area. Hydrocarbons appear to be mainly derived from biogenic terrestrial sources as evidenced by an inverse correlation of concentration with increasing distance from the mainland and a strong odd carbon preference in the n-alkanes. Contribution from petroleum sources, while minor, was most noticeable between Halifax and Emerald Bank. There is also evidence that the hydrocarbon composition at abandoned exploratory drilling sites has been slightly altered.     

Comparison of crude oils and their alteration products

A simple method is proposed for using gas Chromatographic data on the high molecular weight saturated fractions of crude oils to make comparisons of source materials, migration mechanisms and, in particular, alteration processes within reservoirs. The preferential loss of normal alkanes by bacterial attack on a light crude is one of several processes readily followed using this scheme.     

Primary fractionation of elements among iron meteorites

The primary fractionation process in iron meteorites is that responsible for the distribution of elements between the groups, most notably Ga and Ge, which show concentration ranges of 10³ and 10⁴ respectively. To investigate the cause of the primary fractionation, concentrations of 16 elements were converted to relative abundances by dividing the element/Ni ratio by the CI chondrite ratio. These abundances were plotted on logarithmic graphs with data for each group (except IB and IIICD) and each cluster of closely related anomalous irons averaged.Co, P, Au, As, Cu, Sb, Ge and Zn are positively correlated with Ga. For most groups (except IA, IC and IIAB) relative abundances of these elements tend to decrease from about 1 in approximately the order listed above. This is the expected order in which these elements will condense into Fe, Ni during equilibrium nebular condensation. Mean relative abundances of refractory elements in groups generally lie within a narrow range of 0.5–2, and are uncorrelated with Ga. Although the equilibrium model may be only a gross approximation, it suggests that most primary fractionation did occur during nebular condensation.The anomalous irons are essential for defining many of the primary fractionation trends. On several element-Ga graphs the displacements of the anomalous irons from the primary curves indicate that these irons experienced the same secondary fractionation process (probably fractional crystallization) that produced the trends within most groups. The anomalous irons appear to be samples from over 50 minor groups, which have similar histories to the 12 major groups.     

Chemical exchange during hydrothermal alteration of basalt by seawater—I. Experimental results for major and minor components of seawater

Fresh mid-ocean ridge basalt of varying crystallinity has been powdered and reacted with seawater and an artificial Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. Water/rock mass ratios of 1–3 were used and durations ranged from 2 to 20 months.These time periods were sufficient for most elements to approach a steady-state concentration in solution which was determined by equilibrium with alteration minerals (Mg, SiO₂, SO₄), by rate of formation of these minerals (Na, Ca), or by depletion from the rock (K, B, Ba). The resulting solutions closely resemble the brines from the basalt-seawater geothermal system at Reykjanes, Iceland. Mg was almost completely removed from seawater into the alteration products smectite, tremolite-actinolite, or talc. Sulfate also was removed to low concentrations, both by precipitation of anyhydrite and by reduction to sulfide. Net transfer of Na from seawater into solids occurred in most experiments by formation of sodic feldspar and possibly analcime. Sr was removed from seawater in some experiments but showed no change or a small gain in others. SiO₂, Ca, K, Ba, B and CO₂ were leached from basalt and enriched in solution. SiO₂ concentrations were controlled by saturation with quartz at 300°C and above. The principal Ca-bearing phases which formed were anhydrite, the hydrated Ca-silicate truscottite, tremolite-actinolite, and possibly wairakite. No K-rich phases formed. For some minerals the crystallinity of the starting basalt affected the amount which formed.Removal of Mg from seawater into solid alteration products occurred rapidly and was balanced largely by leaching of Ca from basalt. Net transfer of Na from seawater into solids occurred more slowly and was balanced mainly by leaching of additional Ca from basalt. Thus, reaction between seawater and basalt at low water/rock ratios can be considered to consist of two exchanges: Mg for Ca, and Na for Ca.