The role of fluids in the metamorphism of komatiites,Agnew nickel deposit,western Australia

The Agnew nickel sulfide deposit is spatially associated with a lenticular body of ultramafic rocks which shows a concentric zonation in metamorphic mineralogy. Olivine + tremolite + chlorite + cummingtonite ±enstatite assemblages occur at the margin of the ultramafic lens, giving way to olivine + anthophyllite, olivine + talc and olivine + antigorite assemblages successively inwards. These rocks are interpreted as having crystallized from komatiitic lavas, and exhibit a spectrum of compositions from those of original flow tops to pure olivine adcumulates. The relative modal abundances of metamorphic olivine, tremolite and chlorite reflect original proportions of cumulus olivine and komatiite liquid in the protolith. Peak metamorphic conditions are estimated at 550° C, based on garnet-biotite thermometry, at a maximum pressure of 3 kb. This temperature falls within the narrow range over which metamorphic olivine may co-exist with enstatite, anthophyllite, talc or antigorite depending upon the fugacity of water in the metamorphic fluid. The observed mineralogical zonation is therefore attributed to infiltration by CO₂-rich fluids, generated by decarbonation of talc-carbonate rocks formed during pre-metamorphic marginal alteration of the ultramafic lens. Metamorphic fluids were essentially binary mixtures of water and CO₂, with minor H₂S having a maximum partial pressure less than 1 percent of total pressure. Enstatite-bearing assemblages formed in the presence of CO₂-rich fluids at fluid: rock volume ratios close to one, while anthophyllite, talc and antigorite bearing assemblages formed in the presence of progressively more water-rich fluids at progressively lower fluid-rock ratios.     

Volatile C1C7 organic compounds in an anoxic sediment core from the Pettaquamscutt River (Rhode Island,U.S.A.)

Surface sediments from an anoxic marine environment, the Upper Basin of the Pettaquamscutt River, Rhode Island, were analyzed for volatile organic compounds in the C₁C₇ range. The compounds identified included methane, ethane, alkenes (C₂C₅), carbon disulfide, cyclopentane, 3-methylpentane, methylfuran, aldehydes and ketones. Ethane, methylfuran, and most of the aldehydes and ketones showed maxima at the sediment water interface. Methane levels were very high-10–100 times greater than observed in most other surface sediments examined in this laboratory.     

Mantle-derived volatiles in continental crust: the Massif Central of France

CO₂-rich gases and groundwaters from springs and boreholes originating within the basement of the Massif Central have variable³He/⁴He ratios with correspondingR/R_a values ranging from 0.8 to 5.5 and 0.3 to 2.8 respectively, indicating the presence of a significant component of mantle helium. Molar concentrations of rare gases in the CO₂-rich gases are approximately 5 orders of magnitude greater than in the waters and suggest that a near-surface Henry's Law fractionation has occurred between exsolving CO₂ and water.δ¹³C values of the CO₂-rich gases are in the range −4.2 to −6.1‰, i.e. in that range normally attributed to mantle carbon, but which could also represent an average crustal composition and therefore do not discriminate between mantle and crustal sources.C/³He ratios show 4 orders of magnitude variation from 1.4 × 10¹² to 5 × 10⁸ and, compared to a mantleC/³He ratio of 10⁹, indicate that either a complex fractionation has occurred between mantle helium and mantle CO₂ or more likely that mantle rare gases have been diluted by large quantities of CO₂ with an average crustal carbon isotope composition. The regional distribution of³He and C does not show any obvious relationship to age or proximity of volcanic centres or major faults, suggesting that mantle-derived C and He components decoupled from their silicate melt sources at some depth.The results from this area of active fluid circulation suggest that C-isotope data derived from metamorphic terrains should be interpreted with great caution, but that input of some mantle-derived carbon is expected to accompany crustal extension.     

Exploration of structure and bonding in stishovite with fourier and pseudoatom refinement methods using single crystal and powder X-ray diffraction data

The structure and bonding in stishovite, SiO₂, is explored with Fourier summation and pseudoatom refinement of merged x-ray single crystal and powder diffraction data. Replacement of the 25 lowest-angle, highly extinction-affected, single crystal reflections with structure factors obtained from low-extinction powder diffraction data has resulted in a significant improvement in the analysis compared with earlier studies. The deformation electron density, total electrostatic potential and total and valence electron densities are mapped. Accumulations of electron density are observed in both SiO bonds, together with non-bonding features displayed about the oxygen on both sides of a plane formed by three bonds with Si. Deficits of electron density between O atoms across the shared-edges are rationalized in terms of the Pauli exclusion principle. There is no evidence for strong repulsion of Si atoms across the same ring. The total electrostatic potential has a continuous low value for the vacant channels in the structure along c with localized minima between O atoms on opposite sides of the channel. The sizes of Si and O are related to the electron density and to the electrostatic potential.     

Spherical capacitor hypothesis of the earth's electric field

Summary Stemming from the suggestion that the earth-ionospheric fair weather field arises from the lowest order resonant excitation of the earth-ionosphere cavity by lightning, it is shown that the same field is generated through electrostatic induction by equivalent charge dipoles from thunderclouds in the earth's atmosphere. An electrostatic induction model was used to derive from known worldwide thunderstorm data the magnitude of the expected earth-ionosphere fair weather potential. A value of only approximately one third of the observed potential was obtained. Possible sources of the discrepancy are suggested.     

Survival of sea anemones in Bunker C fuel

Sea anemones (Anthopleura elegantissima) can withstand submersion in Bunker C fuel oil for up to 1 h without visible adverse effects. The wet, mucus-covered tissues of the sea anemones may repel oil. During recovery, the sea anemones expand the column, evert the tentacles and reattach. A dahlia anemone (Tealia lofotensis) withstood immersion in oil for 15 min. The ability to withstand immersion in oil may confer an ecological advantage to sea anemones in contaminated areas.     

Variation in copepod species assemblage distributions: The utility of the log-normal approach

Pelagic copepod species distributions were found to vary in relation to an environmental gradient. As suggested by Gray, systematic changes were noted in the skewness of the log-normal. However, no systematic changes in the standard of deviation of the log-normal were noted. The data indicate that such assemblages ill-fit Preston's ‘canonical’ expectation. Further, analysis of changes in the evenness function yielded similar conclusions.