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At least 73 records · Page 4

Rocket ultraviolet spectroscopy of comet Halley and abundance of carbon monoxide and carbon

Two far ultraviolet observations of comet Halley made on 26 February, 1986 and 13 March, 1986 with a sounding rocket experiment are reported. The observed CO spatial profiles can be modelled by a radial outflow model for a parent molecule and suggest that the CO is produced directly from the nucleus of the comet. Using the observed O I emission profile to deduce the H2O production rate, the abundance of CO relative to H2O is found to be 20 percent + or - 5 percent for the first flight and 17 percent + or - 4 percent for the second flight, making CO the second most abundant parent molecule in the coma. The derived production rate of atomic carbon is consistent with that expected from the photodissociation of carbon monoxide.

Woods, T. N.↗

Visible and ultraviolet /800-130 nm/ extinction of vapor-condensed silicate, carbon, and silicon carbide smokes and the interstellar extinction curve

The extinction curves from 800 to 130 nm (1.25-7.7/micron) of amorphous silicate smokes nominally of olivine and pyroxene composition, carbon smokes, and crystalline SiC smokes are presented. The SiC smoke occurred in the low-temperature (beta) cubic structural form. The SiC smoke showed an absorption edge which occurred at significantly longer wavelengths than the calculated extinction profile of the hexagonal SiC form previously used to calculate the interstellar extinction profile. Neither SiC nor amorphous silicates show an extinction band similar to the observed 6.6/micron astronomical extinction band. The infrared absorption peaks for the silicate and SiC samples near 10 microns and 11-13 microns, respectively, were also measured. The ultraviolet to infrared extinction ratio for the amorphous silicate samples is similar to the observed astronomical extinction ratio. The measured extinction ratios for SiC smokes are significantly below the interstellar extinction ratio. The extinction peak of the carbon smokes occurred at 4.0 and 4.25/micron, for samples of mean radii 13 and 6 nm, respectively. The extinction profile is distinctly different from that predicted for graphite grains of the same size, and is similar to that predicted for glassy carbon grains.

Stephens, J. R.↗

Carbon-14 terrestrial ages and weathering of 27 meteorites from the southern high plains and adjacent areas (USA)

We report on a series of 27 C-14 terrestrial ages of meteorites from four states in the central and southwestern U.S. These results were compared to the earlier work of Boeckl (1972). Our results showed that the weathering rate for destruction of meteorites is lower than suggested by Boeckl. We estimate a 'half-life' for removal of meteorites of about 10 to 15 ka, similar to that derived for Roosevelt County meteorites. We also studied the weathering of these meteorites compared to terrestrial age. Only a weak correlation was observed, and for these meteorites the degree of weathering can only be taken as a weak indicator of terrestrial residence time. We also measured the delta-C-13 and C-14 and amount of weathering-product carbonates which show some interesting variations with the length of time the meteorites have been exposed to weathering.

Jull, A. J. T.↗

Molecular Distribution, 13C-Isotope, and Enantiomeric Compositions of Carbonaceous Chondrite Monocarboxylic Acids

The water-soluble organic compounds in carbonaceous chondrite meteorites constitute a record of the synthetic reactions occurring at the birth of the solar system and those taking place during parent body alteration and may have been important for the later origins and development of life on Earth. In this present work, we have developed a novel methodology for the simultaneous analysis of the molecular distribution, compound-specific (delta)(exp 13)C, and enantiomeric compositions of aliphatic monocarboxylic acids (MCA) extracted from the hot-water extracts of 16 carbonaceous chondrites from CM, CR, CO, CV, and CK groups. We observed high concentrations of meteoritic MCAs, with total carbon weight percentages which in some cases approached those of carbonates and insoluble organic matter. Moreover, we found that the concentration of MCAs in CR chondrites is higher than in the other meteorite groups, with acetic acid exhibiting the highest concentration in all samples. The abundance of MCAs decreased with increasing molecular weight and with increasing aqueous and/or thermal alteration experienced by the meteorite sample. The (delta)(exp 13)C isotopic values of MCAs ranged from 52 to +27(0/00), and aside from an inverse relationship between (delta)(exp 13)C value and carbon straight-chain length for C3–C6 MCAs in Murchison, the 13C-isotopic values did not correlate with the number of carbon atoms per molecule. We also observed racemic compositions of 2-methylbutanoic acid in CM and CR chondrites. We used this novel analytical protocol and collective data to shed new light on the prebiotic origins of chondritic MCAs.

Aponte, Jose C.↗

NASA Tech Briefs, March 2004

Topics covered include: 1) Advanced Signal Conditioners for Data-Acquisition Systems; 2) Downlink Data Multiplexer; 3) Viewing ISS Data in Real Time via the Internet; 4) Autonomous Environment-Monitoring Networks; 5) Readout of DSN Monitor Data; 6) Parallel-Processing Equalizers for Multi-Gbps Communications; 7) AIN-Based Packaging for SiC High-Temperature Electronics; 8) Software for Optimizing Quality Assurance of Other Software; 9) The TechSat 21 Autonomous Sciencecraft Experiment; 10) Software for Analyzing Laminar-to-Turbulent Flow Transitions; 11) Elastomer Filled With Single-Wall Carbon Nanotubes; 12) Modifying Ship Air-Wake Vortices for Aircraft Operations; 13) Strain-Gauge Measurement of Weight of Fluid in a Tank; 14) Advanced Docking System With Magnetic Initial Capture; 15) Blade-Pitch Control for Quieting Tilt-Rotor Aircraft; 16) Solar Array Panels With Dust-Removal Capability; 17) Aligning Arrays of Lenses and Single-Mode Optical Fibers; 18) Automatic Control of Arc Process for Making Carbon Nanotubes; 19) Curved-Focal-Plane Arrays Using Deformed-Membrane Photodetectors; 20) Role of Meteorology in Flights of a Solar-Powered Airplane; 21) Model of Mixing Layer With Multicomponent Evaporating Drops; 22) Solution-Assisted Optical Contacting; 23) Improved Discrete Approximation of Laplacian of Gaussian; 24) Utilizing Expert Knowledge in Estimating Future STS Costs; 25) Study of Rapid-Regression Liquefying Hybrid Rocket Fuels; and 26) More About the Phase-Synchronized Enhancement Method.

Source record↗

Limits on the UV Photodecomposition of Carbonates on Mars

The effect of UV (ultraviolet) light on the stability of calcium carbonate in a simulated martian atmosphere was experimentally investigated. Sample cells containing C-13 labeled calcite were irradiated with a Xe arc lamp in 10 mbar of simulated martian atmosphere and a quadrupole mass spectrometer was used to monitor the headspace gases for the production of (13)CO2. We found no experimental evidence of the UV photodecomposition of calcium carbonate in a simulated martian atmosphere. Extrapolating the lower limit of detection of our experimental system to an upper limit of carbonate decomposition on Mars yields a quantum efficiency of 3.5 x 10(exp -8) molecules/photon over the wavelength interval of 190-390 nm and a maximum UV photodecomposition rate of 1.2 x 10(exp -13) kg m(exp -2) s(exp -1) from a calcite surface. The maximum loss of bulk calcite due to this process would be 2.5 nm yr(exp -1). However, calcite is expected to be thermodynamically stable on the surface of Mars and potential UV photodecomposition reaction mechanisms indicate that while calcium carbonate may decompose under vacuum, it would be stable in a CO2 atmosphere. Given the expected stability of carbonate on Mars and our inability to detect carbonate decomposition, we conclude that it is unlikely that the apparent absence of carbonate on the martian surface is due to UV photo decomposition of calcite in the current environment.

Quinn, Richard↗

Carbon and Sulfur Isotopic Signatures of Ancient Life and Environment at the Microbial Scale: Neoarchean Shales and Carbonates

An approach to coordinated, spatially resolved, in situ carbon isotope analysis of organic matter and carbonate minerals, and sulfur three- and four-isotope analysis of pyrite with an unprecedented combination of spatial resolution, precision, and accuracy is described. Organic matter and pyrite from eleven rock samples of Neoarchean drill core express nearly the entire range of delta(sup 13)C, delta(sup 34)S, Delta(sup 33)S, and Delta(sup 36)S known from the geologic record, commonly in correlation with morphology, mineralogy, and elemental composition. A new analytical approach (including a set of organic calibration standards) to account for a strong correlation between H/C and instrumental bias in SIMS delta(sup 13)C measurement of organic matter is identified. Small (2-3 microns) organic domains in carbonate matrices are analyzed with sub-permil accuracy and precision. Separate 20- to 50-micron domains of kerogen in a single approx. 0.5 cu cm sample of the approx. 2.7 Ga Tumbiana Formation have delta(sup 13)C = −52.3 +/- 0.1per mille and −34.4 +/- 0.1per mille, likely preserving distinct signatures of methanotrophy and photoautotrophy. Pyrobitumen in the approx. 2.6 Ga Jeerinah Formation and the approx. 2.5 Ga Mount McRae Shale is systematically 13C-enriched relative to co-occurring kerogen, and associations with uraniferous mineral grains suggest radiolytic alteration. A large range in sulfur isotopic compositions (including higher Delta(sup 33)S and more extreme spatial gradients in Delta(sup 33)S and Delta(sup 36)S than any previously reported) are observed in correlation with morphology and associated mineralogy. Changing systematics of delta(sup 34)S, Delta(sup 33)S, and Delta(sup 36)S, previously investigated at the millimeter to centimeter scale using bulk analysis, are shown to occur at the micrometer scale of individual pyrite grains. These results support the emerging view that the dampened signature of mass-independent sulfur isotope fractionation (S-MIF) associated with the Mesoarchean continued into the early Neoarchean, and that the connections between methane and sulfur metabolism affected the production and preservation of S-MIF during the first half of the planet's history.

isotopic signatures↗

Carbon-Isotopic Dynamics of Streams, Taylor Valley, Antarctica: Biological Effects

We have investigated the role of biological processes in the C-isotopic dynamics of the aquatic ecosystems in Taylor Valley, Antarctica. This cold desert ecosystem is characterized by the complete lack of vascular plants, and the presence of algal mats in ephemeral streams and perennially ice covered lakes. Streams having abundant algal mats and mosses have very low sigma CO2 concentrations, as well as the most depleted delta C-13 values (-4%). Previous work has shown that algal mats in these streams have delta C-13 values averaging -7.01%. These values are similar to those observed in the algal mats in shallow areas of the lakes in Taylor Valley, where CO2 is thought to be colimiting to growth. These low Sigma CO2 concentrations, and delta C(13) signatures heavier than the algal mats, suggest that CO2 may be colimiting in the streams, as well. Streams with little algal growth, especially the longer ones in Fryxell Basin, have higher Sigma CO2 concentrations and much more enriched isotopic signatures (as high as +8%). In these streams, the dissolution of isotopically enriched, cryogenic CaCO3 is probably the major source of dissolved carbonate. The delta C(13) geochemistry of Antarctic streams is radically different from the geochemistry of more temperate streams, as it is not affected by terrestrially produced, isotopically depleted Sigma CO2. These results have important implications for the understanding of "biogenic" carbonate that might have been produced from aquatic ecosystems in the past on Mars.

Neumann, K.↗

Adaptation to high CO2 concentration in an optimal environment: radiation capture, canopy quantum yield and carbon use efficiency

The effect of elevated [CO2] on wheat (Triticum aestivum L. Veery 10) productivity was examined by analysing radiation capture, canopy quantum yield, canopy carbon use efficiency, harvest index and daily C gain. Canopies were grown at either 330 or 1200 micromoles mol-1 [CO2] in controlled environments, where root and shoot C fluxes were monitored continuously from emergence to harvest. A rapidly circulating hydroponic solution supplied nutrients, water and root zone oxygen. At harvest, dry mass predicted from gas exchange data was 102.8 +/- 4.7% of the observed dry mass in six trials. Neither radiation capture efficiency nor carbon use efficiency were affected by elevated [CO2], but yield increased by 13% due to a sustained increase in canopy quantum yield. CO2 enrichment increased root mass, tiller number and seed mass. Harvest index and chlorophyll concentration were unchanged, but CO2 enrichment increased average life cycle net photosynthesis (13%, P < 0.05) and root respiration (24%, P < 0.05). These data indicate that plant communities adapt to CO2 enrichment through changes in C allocation. Elevated [CO2] increases sink strength in optimal environments, resulting in sustained increases in photosynthetic capacity, canopy quantum yield and daily C gain throughout the life cycle.

Non-NASA Center↗

The Orbiting Carbon Observatory (OCO) Mission

This viewgraph presentation gives a general overview of The Orbiting Carbon Observatory (OCO) Mission. The contents include: 1) The Orbiting Carbon Observatory (OCO); 2) Why Measure CO2?; 3) An Uncertain Future; 4) Monitoring CO2 from Space; 5) Validation Program Ensures Accuracy and Minimizes Spatially Coherent Biases; 6) The OCO Instrument; 7) The OCO Spacecraft; 8) Mission Operations and Data Downlink; 9) OCO Data Products; 10) OCO Data Product Summary; 11) OCO in the A-Train; 12) Summary; and 13) Simulated Performance.

Pathfinder Program↗

A search for presolar organic matter in meteorite

The D/H ratios and the C-13/C-12 ratios of acid-insoluble organic matter of 4 meteorites, Ochansk (H4), Plainview (H5), Gladstone (H6) and Odessa (IA), were measured. delta-D values for hydrogen extracted by stepwise combustion were negative, down to -280 deg/infinity. delta-C-13 values were also negative except in the case of the carbon coming off at the highest temperature steps for Plainview and Odessa meteorites. The concentrations of C-13-rich carbon were 3-5 orders of magnitude smaller than those found in Murchison meteorite, suggesting that relic grains of stellar condensates were mostly destroyed in the meteorites examined.

Yang, J.↗

SN 1993J: A Type IIb supernova

The evolution of the bright Type II supernova discovered last year in M81, SN 1993J, is consistent with that expected for the explosion of a star which on the main sequence had a mass of 13-16 Solar Mass but which, owing to mass exchange with a binary companion (a intially approximately 3-5 AU, depending upon the actual presupernova radius and the masses of the two stars) lost almost all of its hydrogen-rich envelope during late helium burning. At the time of explosion, the helium core mass was 4.0 +/- 0.5 Solar Mass and the hydrogen envelope, 0.20 +/- 0.05 Solar Mass. The envelope was helium and nitrogen-rich (carbon-deficient) and the radius of the star, 4 +/- 1 x 10(exp 13) cm. The luminosity of the presupernova star was 3 + 1 x 10(exp 38) ergs/s, with the companion star contributing an additional approximately 10(exp 38) ergs/s. The star may have been a pulsating variable at the time of the explosion. For an explosion energy near 10(exp 51) ergs (KE at infinity) and an assumed distance of 3.3 Mpc, a mass of Ni-56 in the range 0.07 +/- 0.01 Solar Mass was produced and ejected. This presciption gives a light curve which compares favorably with the bolomatric observations. Color photometry is more restrictive and requires a model in which the hydrogen-envelope mass is low and the mixing of hydrogen inward has been small, but in which appreciable Ni-56 has been mixed outward into the helium and heavy-element core. It is possible to obtain good agreement with B and V light curves during the first 50 days, but later photometry, especially in bands other than B and V, will require a non-local thermo-dynamic equilibrium (LTE) spectral calculation for comparison. Based upon our model, we predict a flux of approximately 10(exp -5)(3.3 Mpc/D)(exp 2) photons/sq cm/s in the 847 keV line of CO-56 at peak during 1993 August. It may be easier to detect the Computonized continuum which peaks at a few times 10(exp -4) photons /s/sq cm/MeV at 40 keV a few months after the explosion (though neither of these signals were, or should have been, detected by the Compton Gamma-Ray observatory (CGRO). The presupernova star was filing its Roche lobe at the time of the explosion and thus its envelope was highly deformed (about 3:2). The companion star is presently embedded in the supernova, but should becopme visable at age 3 yr (perhaps earlier in the ultraviolet) when the supernova has faded below 10(exp 38) ergs/s. Indeed, if 'kicks' have not played an important role, it is still bound to the neutron star.

Woosley, S. E.↗

Carbon and nitrogen isotopic compositions of alkyl porphyrins from the Triassic Serpiano oil shale

The carbon and nitrogen isotopic compositions of seven of the most abundant alkylporphyrins from the Serpiano oil shale (marine, Triassic) were determined. For the C31 and C32 butanoporphyrins, values of delta 13CPDB and delta 15NAIR averaged -24.0% and -3.1%. In contrast, the C31 and C32 methylpropanoporphyrins, DPEP, and a C30 13-nor etioporphyrin had delta 13C and delta 15N values averaging -27.5 and -3.3%, respectively. Carbon and nitrogen isotopic values for kerogen averaged -30.8 and -0.9, whereas those for total extract averaged -31.6, and -4.0%. The butanoporphyrins apparently derive from a biological source different from that giving rise to the other porphyrins, their 13C enrichment not being related to carbon isotopic fractionation accompanying diagenetic reactions. The delta 15N values for all the porphyrins indicate that the depletion of 15N observed in the kerogen is of primary origin. Consistent with the very high abundance of hopanoids and methyl hopanoids in the aliphatic hydrocarbon fraction, it is suggested that cyanobacterial fixation of N2 may have been the main cause of 15N depletion.

NASA Discipline Exobiology↗

The atomic carbon distribution in the coma of Comet Halley

The radial distribution of CO, OI, Ci, and CII emissions in the coma of comet Halley were measured by a long-slit far ultraviolet spectrograph aboard a sounding rocket on 26 Feb. and 13 Mar. 1986. While the CO profiles strongly suggest that CO is vaporized directly from the nucleus, the observed carbon distribution is not consistent with a radial outflow model of CO, suggesting an additional source of atomic carbon in the inner coma. Based on the in situ plasma measurements from the Vega and Giotto spacecraft, it is possible that this additional source of carbon could be the recombination of ionized CO in the inner coma.

Woods, T. N.↗

Dual alloy interface stability

Powder metallurgy dual alloy fabrication is applied to combinations of superalloys having a high iron, and low strategic metal content, with standard nickel base superalloys, containing the strategic metals chromium, cobalt, and columbium. The possibility of combining Alloy 901 (12 percent Cr, 36 percent Fe, 0 percent Co, and 0 percent Cb) with turbine disk alloys Rene 95 (13 percent Cr, 8 percent Co, and 4 percent Cb) or low carbon astroloy (L.C.A.; 15 percent Cr, 17 percent Co, and 0 percent Cb) is investigated. Preliminary results for combinations show that a strong interface with rapid diffusion is obtained between alloys and that the standard heat treatments for either alloy may be satisfactory.

Harf, F. H.↗

Carbon kinetic isotope effect in the reaction of CH4 with HO

The carbon kinetic isotope effect in the CH4 + HO reaction is measured experimentally and the use of carbon isotope ratios to diagnose atmospheric methane is examined. The chemical, photolysis, and analytical experimental conditions and procedures are described. It is determined that the CH4 + HO reaction has a carbon kinetic isotope effect of 1.010 + or 0.007 for k(12)k(13) (rate constants ratio) at 297 + or - 3 K. This value is compared with the data of Rust and Stevens (1980). Causes for the poor correlation between the data at high methane conversions are discussed. It is supposed that the difference between the k(12) and k(13) values is due to a difference in the activation energy of the two reactions.

Davidson, J. A.↗