Proximate Constituents, Biomass, and Energy in Posidonia oceanica (Potamogetonaceae)

Abstract. The proximate composition of the various components of Posidonia oceanica is given in terms of gravimetric and energetic level and amount of plants from 2 depths at Port-Cros (Var. France). The level of proximate constituents differed little between the leaves (regardless of age) and the roots, but the rhizome contained much more soluble carbohydrate and less structural carbohydrate and ash. Because of this, the energy level in the leaves was more in terms of organic material and less in terms of total material than the energy level in the rhizome. The leaves of a P. oceanica shoot at 2 m depth in July contained 1.6 g organic material. 29.0 kJ. The weight and energy of the soluble carbohydrate in the rhizome from the base of the leaves to the 18th sheath scale decreased by ca. 40% from October to March and increased by ca. 100% from March to July.     

Oil and gas resource assessment: The linkage between geological analysis and discovery process model results

Two widely-used techniques to estimate the volume of remaining oil and gas resources are discovery process modeling and geologic assessment. Both were used in a recent national assessment of oil and gas resources of the United States. Parallel estimates were obtained for 27 provinces. Geological-based estimates can typically see into areas not available to discovery process models (that is areas with little or no exploration history) and thus, on average, yield higher estimates. However, a linear relation does exist between the mean estimates obtained from these two methods. In addition, other variables were found in a multiple regression model that explained much of the difference. Thus, it is possible to perform discovery process modeling and adjust the estimates to yield results that might be expected from geological-based assessments.     

Diamondiferous eclogites from Yakutia,Siberia: evidence for a diversity of protoliths

Major-element and REE compositions of 14 diamondiferous eclogites from the Udachnaya kimberlite in Yakutia, Siberia have been determined by electron microprobe and secondary ion mass spectrometer (SIMS). Based on previous clinopyroxene classification schemes (e.g., Taylor and Neal 1989), all of these eclogite xenoliths belong to Group B/C, although some of the garnet compositions and mineral REE abundances are inconsistent with the indicated groups. This demonstrates the inadequacy of the classification scheme based on African eclogites for application to Siberian samples. Because of the coarse grain size of the Udachnaya nodules, meaningful modal abundances could not be obtained. However, reconstructed REE compositions using various garnet: clinopyroxene ratios demonstrate relative insensitivity to changes in mode for common eclogitic assemblages. Many of these reconstructed REE compositions show LREE depletions. Some depletions are consistent with an origin (either directly or through partial melting) as normal or Type-I ocean floor basalt. Others, however, require material of eclogitic or pyroxenitic affinities to undergo partial melting; this facilitates the depletion of LREE while leaving the HREE at nearly original levels. Many of the eclogites of South Africa are consistent with a protolith of anomalous or Type II ocean floor basalt. This fundamental difference between the two regions is the likely cause of the inconsistencies with the chemicallybased classification.     

High spectral resolution ground-based observations of Venus in the 450- to 1250-cm−1 region

Ground-based observations of Venus were made with a 5-cm drive Michelson interferometer during December 1970 and December 1973. The thermal emission spectrum of the central portion of the apparent disk was recorded from 450–1250 cm^?1 with an apodized spectral resolution of 0.25 cm^?1. All statistically significant sharp line absorption features in the spectrum have been identified with gaseous CO₂. Comparison between the observed spectrum and a synthetic spectrum computed from a model atmosphere, assuming gaseous CO₂ and a sulfuric acid haze as opacity sources, indicates good agreement. A broad diffuse absorption feature associated with the sulfuric acid haze is evident in the 870- to 930 cm^?1 region. With the exception of the rotational lines of the 927-cm^?1 CO₂ band, the above feature appears as a continuum down to 0.25 cm^?1 resolution. In the 750- to 1250-cm^?1 range, the spectrum exhibits moderate thermal contrast with maximum brightness temperatures of 234–238°K occurring near 825 cm^?1. These temperatures are in general agreement with previous measurements.     

Synchrotron radio emission from Uranus and Neptune

A number of charged-particle radiation belt models for Uranus and Neptune are postulated, and the synchrotron emission spectrum for each is calculated over the frequency range 18.75 to 2400 MHz. Although no radio observations of these planets exist at frequencies below 1400MHz, available observations are used in conjunction with the synchrotron calculations to establish a rough upper limit to the size and strength of the planets' magnetic field strength and radiation belt intensity. The magnitude of synchrotron radio emission expected in many of the models is within the detection range of several existing ground-based telescopes, at decimetric and metric wavelengths.     

Investigating the scale of structural controls on chlorinated hydrocarbon distributions in the fractured-porous unsaturated zone of a sandstone aquifer in the UK

Contaminant migration behaviour in the unsaturated zone of a fractured porous aquifer is discussed in the context of a study site in Cheshire, UK. The site is situated on gently dipping sandstones, adjacent to a linear lagoon historically used to dispose of industrial wastes containing chlorinated solvents. Two cores of more than 100 m length were recovered and measurements of chlorinated hydrocarbons (CHCs), inorganic chemistry, lithology, fracturing and aquifer properties were made. The results show that selecting an appropriate vertical sampling density is crucial both to providing an understanding of contaminant pathways and distinguishing whether CHCs are present in the aqueous or non-aqueous phase. The spacing of such sampling should be on a similar scale to the heterogeneity that controls water and contaminant movement. For some sections of the Permo-Triassic aquifer, significant changes in lithology and permeability occur over vertical distances of less than 1 m and samples need to be collected at this interval, otherwise considerable resolution is lost, potentially leading to erroneous interpretation of data. At this site, although CHC concentrations were high, the consistent ratio of the two main components of the plume (tetrachloroethene and trichloroethene) provided evidence of movement in the aqueous phase rather than in dense non-aqueous phase liquid (DNAPL).     

Formation of refractory inclusions by evaporation of condensate precursors

Berman’s (1983) activity-composition model for CaO-MgO-Al₂O₃-SiO₂ liquids is used to calculate the change in bulk chemical and isotopic composition during simultaneous cooling, evaporation, and crystallization of droplets having the compositions of reasonable condensate precursors of Types A and B refractory inclusions in CV3 chondrites. The degree of evaporation of MgO and SiO₂, calculated to be faithfully recorded in chemical and isotopic zoning of individual melilite crystals, is directly proportional to evaporation rate, which is a sensitive function of P_H2, and inversely proportional to the droplet radius and cooling rate. When the precursors are partially melted in pure hydrogen at peak temperatures in the vicinity of the initial crystallization temperature of melilite, their bulk chemical compositions evolve into the composition fields of refractory inclusions, mass-fractionated isotopic compositions of Mg, Si, and O are produced that are in the range of the isotopic compositions of natural inclusions, and melilite zoning profiles result that are similar to those observed in real inclusions. For droplets of radius 0.25 cm evaporating at P_H2 = 10⁻⁶ bar, precursors containing 8 to 13 wt.% MgO and 20 to 23% SiO₂ evolve into objects similar to compact Type A inclusions at cooling rates of 2 to 12 K/h, depending on the precise starting composition. Precursors containing 13 to 14 wt.% MgO and 23 to 26% SiO₂ evolve into objects with the characteristics of Type B1 inclusions at cooling rates of 1.5 to 3 K/h. The relatively SiO₂-poor members of the Type B2 group can be produced from precursors containing 14 to 16 wt.% MgO and 27 to 33% SiO₂ at cooling rates of <1 K/h. Type B2’s containing 27 to 35 wt.% SiO₂ and <12% MgO require precursors with higher SiO₂/MgO ratios at MgO > 15% than are found on any condensation curve. The characteristics of fluffy Type A inclusions, including their reversely zoned melilite, can only be understood in the context of this model if they contain relict melilite.