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At least 127 records · Page 7

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NASA NTRS2013

Extraterrestrial Amino Acids Identified in Metal-Rich CH and CB Carbonaceous Chondrites from Antarctica

Carbonaceous chondrites contain numerous indigenous organic compounds and could have been an important source of prebiotic compounds required for the origin of life on Earth or elsewhere. Extraterrestrial amino acids have been reported in five of the eight groups of carbonaceous chondrites and are most abundant in CI, CM, and CR chondritesbut are also present in the more thermally altered CV and CO chondrites. We report the abundance, distribution, and enantiomeric and isotopic compositions of simple primary amino acids in six metal-rich CH and CB carbonaceous chondrites that have not previously been investigated for amino acids: Allan Hills (ALH) 85085 (CH3), Pecora Escarpment(PCA) 91467 (CH3), Patuxent Range (PAT) 91546 (CH3), MacAlpine Hills (MAC) 02675(CBb), Miller Range (MIL) 05082 (CB), and Miller Range (MIL) 07411 (CB). Amino acid abundances and carbon isotopic values were obtained by using both liquid chromatography time-of-flight mass spectrometry and fluorescence, and gas chromatography isotope ratiomass spectrometry. The (delta D, delta C-13, delta N-15) ratios of multiple amino acids fall outside of the terrestrial range and support their extraterrestrial origin. Extracts of CH chondrites were found to be particularly rich in amino acids (1316 parts per million, ppm) while CB chondrite extracts had much lower abundances (0.22 ppm). The amino acid distributions of the CH and CB chondrites were distinct from the distributions observed in type 2 and 3 CM and CR chondrites and contained elevated levels of beta-, gamma-, and delta-amino acids compared to the corresponding alpha-amino acids, providing evidence that multiple amino acid formation mechanisms were important in CH and CB chondrites.

Burton, Aaron S.↗

DOE OSTI2025

Mineral-Associated Organic Matter Concentration Beneath Northern Temperate Trees Varies by Mycorrhizal Type and Leaf Habit

Mycorrhizal fungi are important drivers of soil organic matter dynamics, but it can be difficult to isolate the effects of the fungi themselves from covarying traits of their host trees. For example, many trees with an evergreen leaf habit associate with ectomycorrhizal (ECM) fungi, while many deciduous tree species associate with arbuscular mycorrhizal (AM) fungi. Because leaf habit influences the quantity and quality of organic matter inputs to soil, it is often an important factor in soil carbon and nitrogen dynamics, and thus can mask the effects of mycorrhizal fungi on soil organic matter processes. We evaluated how tree mycorrhizal associations and leaf habit separately influence the amount and composition of mineral-associated organic matter (MAOM) and particulate organic matter (POM) in forest soils in New Hampshire and Vermont, USA. We measured carbon (C) and nitrogen (N) concentrations and C/N ratios of three soil density fractions beneath six tree species that vary in mycorrhizal association and leaf habit. We found lower concentrations of MAOM C and N beneath evergreen vs. deciduous trees, but only for tree species associating with AM fungi. Further, MAOM C/N was higher beneath evergreen trees and beneath trees with ECM fungi rather than AM fungi. Furthermore, these results add to the growing body of support for mycorrhizal fungi as mediators of soil organic matter dynamics, suggesting that the MAOM fraction is more sensitive to leaf habit beneath AM-associated versus ECM-associated trees. Because MAOM decomposition is thought to be less responsive than POM decomposition to changes in soil temperature and moisture, differences in the tendency of AM- and ECM-dominated forests to support MAOM formation and persistence may lead to systematic differences in the response of these forest types to ongoing climate change.

54 ENVIRONMENTAL SCIENCES↗

NASA NTRS1987

Diversity and similarity of comets

The evolution of comets from an early stage where they were all similar, to the later diversity is reviewed. The elemental abundances of all pristine comets are likely to be primitive, that is in solar abundance ratios for all elements including C, N, O, S, but with the exception of H (and assumedly He and Ne) that are severely depleted. The solid phase was originally in very fine grains, typically 0.1 micron or less, eventually sintered into larger grain clusters. The volatile phase contains H, C, N, O, and S molecules frozen in the pores of the grain clusters; cosmic ray plus solar irradiation changes the volatile to refractory ratio of the crust. Differences in dust tails, in plasma tails, in photometry between young and old comets, and in the variable carbon depletion of the gas phase seem to be induced by the decay processes.

Delsemme, A. H.↗

DOE OSTI2024

Large-Volume Injection and Assessment of Reference Standards for n -Alkane δD and δ 13 C Analysis via Gas Chromatography Isotope Ratio Mass Spectrometry

Compound-specific stable isotope analysis of hydrogen (δD) and carbon (δ 13 C) in organic compounds is a valuable tool in biogeochemical research. A key limitation of this method is the relatively large amount of sample required to achieve desirable precision. We developed a large-volume (20 μL) injection method that allows for high throughput analysis of less concentrated samples and tested it for δ 13 C and δD measurements of n-alkanes. We also conducted a comparison of reference standards and assessed several methods to normalize and correct n-alkane δD and δ13C measurements. The mean precision of the δD method based on 233 environmental n-alkane samples (two to three replications per sample) is 4.0‰ (1σ, estimated from the weighted mean of the pooled unbiased standard deviations) and 0.46‰ (1σ) for δ 13 C from 37 environmental samples (two to three replications per sample). The evaluation of reference standards shows that the use of n-alkane standards with large offsets in δD values in adjacent n-alkane chains can lead to biases in measurement correction. The large-volume injection method shows good reproducibility of δ 13 C and δD measurements of n-alkanes and reduces the required sample concentration by about 80%. We propose that for δD measurements, a reference standard set should be used in which each reference standard has a limited range of δD values and no adjacent n-alkane chains, to minimize memory effects.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

NASA NTRS1979

Interstellar absorption lines in the spectrum of Gamma Velorum

Copernicus scans of selected interstellar absorption lines in the UV spectrum of Gamma Vel are analyzed, together with ground-based data, to obtain column densities for various ion states of C, N, O, Na, Mg, Al, Si, P, S, Cl, Ar, Ca, Mn, Fe, and CO. N I and O I are fitted to a single empirical curve of growth with a velocity parameter (b) of 8 km/s; Mg II, Si II, P II, S II, Mn II, and Fe II are fitted to another curve with b between 3 and 9 km/s. Abundance determinations relative to H I show that: (1) C, N, P, S, and Ar are probably close to their solar values; (2) O may be depleted by about a factor of 2; (3) Mg, Al, Si, Cl, Mn, and Fe are depleted by a factor of 4 or more: (4) Al is depleted by at least a factor of 10 in the H II region; and (5) both N V and O VI are present, but not C IV. The N V/O VI ratio implies that the electron temperature in the H II region is about 275,000 K.

Morton, D. C.↗

NASA NTRS1993

Interstellar graphite in Murchison: Continued search for isotopically distinct components

We have measured C-, N-, and O-isotopic ratios of individual graphite grains from the Murchison density fractions KFB1 (2.1-2.15 g/cc) and KFC1 (2.15 -2.20 g/cc). According to the C-isotopic composition, KFC1 consists of two populations: one has light C while the other has heavy C. In addition to these two populations, KFB1 also contains grains whose C-isotopic ratios are approximately normal. In view of these isotopic distributions, it is difficult to understand why the Kr-isotopic compositions of these two separates are so different. In contrast to the lighter density fractions KE1 (1.6-2.05 g/cc) and KFA1 (2.05-2.10 g/cc), the separates KFB1 and KFC1 do not seem to contain many grains with significant O-18 excess.

Amari, Sachiko↗

NASA NTRS1992

Observations of highly ionized gas in the Galactic halo

A sample of high-quality sight lines is studied by means of IUE spectra to study the formation of Si IV, C IV, and N V in the Galaxy and constrain the mechanisms of halo gas formation. High-dispersion IUE spectra are taken for 12 objects to give combined spectra for studying the halo gas along the sight lines. N V absorption is reported in 10 of the sightlines suggesting that hot collisionally ionized gas dominates the Galactic halo. Analyses are conducted to derive the Doppler-spread parameters of the Si IV, C IV, and N V components that are theorized to dominate the collisionally ionized gas. The observed column-density ratios of the high ions are given and shown to be generally constant throughout the Galaxy with no variation according to the distance of the absorbing gas from the Galactic plane. Existing photoionization and collisional models cannot simultaneously predict the column densities and ratios of Si IV, C IV, and N V. It is concluded that the implementation of self-ionization and other mechanisms could make the models more effective.

Sembach, Kenneth R.↗

DOE OSTI2022

Synergistic Electrocatalytic Syngas Production from Carbon Dioxide by Bi‐Metallic Atomically Dispersed Catalysts

Abstract The production of syngas by traditional processes such as steam methane reforming is energetically intensive and produces a large amount of CO 2 emissions. In contrast, the electrochemical CO 2 reduction reaction (CO 2 RR) enables the carbon neutral production of syngas at ambient conditions. Among non‐precious metal catalysts, metal‐nitrogen‐carbon electrocatalysts are inexpensive and highly selective towards syngas production. This study examined the selectivity of mono‐ and bi‐metallic (M−N−C, M=Fe, Mo or FeMo) electrocatalysts towards syngas production. The ratio of the CO : H 2 in the syngas was tuned by modifying the ratio of the metallic precursors in the bi‐metallic FeMo−N−C catalysts, tailoring the catalysts’ selectivity towards the CO 2 RR or the hydrogen evolution reaction (HER). The catalyst synthesis temperature(s) were considered as they influence the catalyst morphology and activity. Further, the dependence of the ratio of CO : H 2 in the syngas as a function of the potential was explored for the different bi‐metallic catalysts. This work showed that by tailoring both the ratio of Fe : Mo in the bi‐metallic catalyst and optimizing the reductive potential, a CO : H 2 ratio between 0.25 to 5 was achievable. This study demonstrated a novel approach in which the ratio of the product syngas composition could be tailored in a single reaction, without the need for further downstream processing to reach a desired composition.

Delafontaine, Laurent↗

NASA NTRS1980

Comparative energy spectra of z equals 3-8 nuclei in the energy range 200 MeV/nuc to 3 GeV/nuc

The energy spectra and charge ratios of Li, Be, B, C, N, and O nuclei in the energy range 200 MeV/nuc to 3 GeV/nuc are examined with measurements obtained during a 50 hour balloon flight in 1977 from a telescope containing several scintillation and Cerenkov counters. The ratios Li/C, Be/C, and B/C are compared with predictions based on the leaky box interstellar propagation model showing that the ratios steadily increase in the apparent interstellar matter path length down to energies of about 400 to 600 MeV/nuc, where it is between 6.5 and 7.5 g/square cm. The effects of solar modulation upon the ratios are considered for energies less than about 1 GeV/nuc as well as for a modulation parameters of phi not less than 400 MV. By examining the ratios Li/Be, Li/B, and Be/B as a function of energy, it is shown that the Li/Be ratio is most sensitive to the solar modulation effects, and that the observed changes in this ratio with energy can be explained by a relatively large modulation consistent with a phi equal to 400 MV in 1977.

Webber, W. R.↗

NASA NTRS1981

The low-energy galactic cosmic ray carbon, nitrogen, and oxygen isotopic composition

It is found that C, N, and O elemental and isotopic ratios in the galactic cosmic rays measured near the earth with the IMP 7 telescope of the University of Chicago have had the values N/O = 0.25 + or 0.02; C/O = 1.06 + or - 0.03; C-13/C = 0.04-0.10; N-15/N = 0.47 + or - 0.06; and O-18/O less than or equal to 0.03. It is noted that these results are confirmed by IMP 8 measurements. The measurements are extrapolated back to the cosmic ray source using exponential and truncated exponential path length distributions whose parameters have been determined by fitting cosmic ray B/C and sub-Fe/Fe ratios measured previously.

Guzik, T. G.↗

NASA NTRS1986

Solar wind carbon, nitrogen and oxygen abundances measured in the earth's magnetosheath with AMPTE/CCE

The solar wind number density ratios of C(6+) + C(5+) and N(7+) + N(6+) + N(5+) relative to O(8+) + O(7+) + O(6+) have been measured for the first time using data from the Charge-Energy-Mass Spectrometer on the AMPTE/CCE spacecraft during four solar active periods from Sept. 19 to Nov. 1, 1984 when CCE traversed the subsolar magnetosheath of the compressed magnetosphere. It is found that the average values of the density ratios of C/O and N/O to be 0.43 + or - 0.03 and 0.15 + or - 0.06, respectively. These ratios, as well as the average He(2+)/O ratio of 43 + or - 5 for these same time periods, are in excellent agreement with Solar Energetic Particles (SEP) abundance ratios as well as SEP-derived coronal abundances of these elements. The solar wind C/O ratio is substantially below the generally accepted photospheric value of 0.60.

Gloeckler, G.↗

DOE OSTI2025

Impact of Thermonuclear Reaction Rate Uncertainties on the Identification of Presolar Grains from Classical Novae

Approximately 30%–40% of classical novae generate dust between 20 and 100 days following the eruption. However, there has yet to be a definitive identification of presolar stardust grains originating from classical novae. While multiple studies have suggested a nova origin for specific grains, aligning simultaneously all measured isotopic ratios of a specific grain with those predicted from simulations remains challenging. Using Monte Carlo simulations, this work investigates how uncertainties in thermonuclear reaction rates influence the isotopic ratios predicted in simulations of classical novae, specifically impacting the identification of presolar grains. In particular, we address two questions: (i) What is the impact of uncertainties in reaction rates on the range of isotopic ratios predicted by classical nova simulations? (ii) Which reaction rate uncertainties most significantly influence the predicted abundance ratios in presolar grains? Our results show that current reaction rate uncertainties affect the isotopic ratios of 12 C/ 13 C, 14 N/ 15 N, 16 O/ 17 O, 16 O/ 18 O, 24 Mg/ 25 Mg, 24 Mg/ 26 Mg, 26 Al/ 27 Al, and 28 Si/ 29 Si by less than 20% in either carbon–oxygen or oxygen–neon (ONe) novae, especially when considering the mixing of matter throughout the entire envelope. However, the isotopic ratios of 28 Si/ 30 Si, 32 S/ 33 S, and 32 S/ 34 S in ONe novae are exceptions: their variability greatly exceeds a factor of 2 due to the uncertainties in the reaction rates of 30 P(p,γ) 31 S, 33 S(p,γ) 34 Cl, and 34 S(p,γ) 35 Cl, respectively. These results highlight the significant influence of specific reaction rates on the predicted abundance ratios and underscore the necessity for accurate nuclear measurements to reduce these uncertainties.

Classical novae↗

NASA NTRS1989

The C-12/C-13 abundance ratio in Comet Halley

The individual (C-13)N rotational lines in Comet Halley are resolved using high-resolution spectra of the CN B2Sigma(+)-X2Sigma(+) (0,0) band. The observe C-12/C-13 abundance ratio excludes a site of origin for the comet near Uranus and Neptune and suggests a condensation environment quite distinct from other solar system bodies. Two theories are presented for the origin of Comet Halley. One theory suggest that the comet originated 4.5 Gyr ago in an inner Oort cloud at a heliocentric distance greater than 100 AU where chemical fractionation led to the C-13 enrichment in the CN parent molecule prior to condensation of the comet nucleus. According to the other, more plausible theory, the comet nucleus condensed relatively recently from the interstellar medium which has become enriches in C-13 and was subsequently gravitationally captured by the solar system.

Wyckoff, Susan↗

DOE OSTI2020

Fission TPC cross section ratio results [Abstract]

The fission TPC was designed for precision fission cross section ratio measurements. The high-fidelity 3D particle tracking data is used to conduct a detailed analysis of the uncertainty contributions. In this contribution a brief overview of the instrument was presented. The results of the 238 U(n,f)/ 235 U(n,f) cross section ratio measurement published in [Phys. Rev C 97, 034618 (2018)] were reviewed and the preliminary status of the 239 Pu(n,f)/ 235 U(n,f) cross section ratio measurement was shown.

238U(n,f)/235U(n,f) cross section ratio↗

DOE OSTI2026

Effects of 9.5 years warming on SOC concentration and composition in bulk soil and density fractions

Original data of whole-soil warming experiment after 9.5 years at Blodgett Forest Research Station. The Blodgett Forest is a mixed coniferous temperate forest with Mediterranean climate. The annual air temperature is 12.5℃ and the annual precipitation is 1774 mm yr-1- The soil is mesic ultic Alfisol of granitic origin, equivalent to Dystric Cambisol according to The World Reference Base for Soil Resources (WRB) system. The soil is warmed down to 1 m at + 4℃ by vertically installed heating cables. At the time of soil sampling on 1 May 2023, the whole-soil warming experiment had been running for approximately 9.5 years, from January 2014 to May 2023. The dataset includes: - Bulk_EA: C, N content, δ13C, and CN ratio of bulk soil; - Density_fractionation: organic carbon concentration, δ13C, and C/N ratio of free light fraction (fLF), occluded ligh fraction (oLF), and heavy fraction (HF); - PCA_DRIFT_AUC: original data of area under the curve (AUC) values of eight carbon bond types integrated on diffuse reflectance infrared fourier transform spectroscopy for each soil sample and soil fraction, which are consequently used for principal component analysis (PCA); - DRIFTS_stability_index: the calculation of aliphatic C–H (3000–2800 cm-1) to aromatic C=C (1670–1600 cm-1) ratios for each bulk soil sample and soil fraction. All data are provided in CSV format and can be viewed using Microsoft Excel.

Climate change↗

NASA NTRS2012

Transformation of Graphitic and Amorphous Carbon Dust to Complex Organic Molecules in a Massive Carbon Cycle in Protostellar Nebulae

More than 95% of silicate minerals and other oxides found in meteorites were melted, or vaporized and recondensed in the Solar Nebula prior to their incorporation into meteorite parent bodies. Gravitational accretion energy and heating via radioactive decay further transformed oxide minerals accreted into planetesimals. In such an oxygen-rich environment the carbonaceous dust that fell into the nebula as an intimate mixture with oxide grains should have been almost completely converted to CO. While some pre-collapse, molecular-cloud carbonaceous dust does survive, much in the same manner as do pre-solar oxide grains, such materials constitute only a few percent of meteoritic carbon and are clearly distinguished by elevated D/H, N-15/N-16, C-13/C-12 ratios or noble gas patterns. Carbonaceous Dust in Meteorites: We argue that nearly all of the carbon in meteorites was synthesized in the Solar Nebula from CO and that this CO was generated by the reaction of carbonaceous dust with solid oxides, water or OH. It is probable that some fraction of carbonaceous dust that is newly synthesized in the Solar Nebula is also converted back into CO by additional thermal processing. CO processing might occur on grains in the outer nebula through irradiation of CO-containing ice coatings or in the inner nebula via Fischer-Tropsch type (FTT) reactions on grain surfaces. Large-scale transport of both gaseous reaction products and dust from the inner nebula out to regions where comets formed would spread newly formed carbonaceous materials throughout the solar nebula. Formation of Organic Carbon: Carbon dust in the ISM might easily be described as inorganic graphite or amorphous carbon, with relatively low structural abundances of H, N, O and S . Products of FTT reactions or organics produced via irradiation of icy grains contain abundant aromatic and aliphatic hydrocarbons. aldehydes, keytones, acids, amines and amides.. The net result of the massive nebular carbon cycle is to convert relatively inert carbonaceous dust from the ISM into the vital organic precursors to life such as amino acids and sugars intimately mixed with dust and ice in primitive planetesimals. Since the number of carbon atoms entering the Solar Nebula as dust exceeds the number of atoms entering the nebula as oxide grains. the formation of large quantities of complex organic molecules may represent the largest single chemical cycle in the nebula.

Nuth, Joseph A., III↗

NASA NTRS1972

Measurements of the Fe-group abundance in energetic solar particles

The abundance of Fe-group nuclei in the energetic solar particles was measured twice in the 24 January 1971 event and once in the 2 September 1971 event. Including earlier results from the 2 September 1966 event, the Fe-group abundance was found to be in the range from 3% to 6% of the oxygen nuclei in the energy interval from 21 to 50 MeV/nucleon, in those events where the Fe-group abundance could be measured. Fe-nuclei have a different charge-to-mass ratio from that of the C, N, O nuclei, so small variations in the Fe abundance in solar particles are expected. In the three exposures where the statistics were adequate to construct an energy spectrum, the Fe-group nuclei were seen to have an energy/nucleon spectrum similar to that of the C, N, O nuclei; however, the energy/nucleon range was limited. The abundance for the Fe-group nuclei is consistent with the present solar spectroscopic abundance estimates.

Bertsch, D. L.↗

NASA NTRS1973

Preparation of polyimides from mixtures of monomeric diamines and esters of polycarboxylic acids

Polyimides having high thermal and oxidative stability are prepared by the reaction of a mixture of monomers comprising (1) a dialkyl or tetraalkyl ester of an aromatic tetracarboxylic acid; (2) an aromatic diamine; and (3) a monoalkyl or dialkyl ester of a dicarboxylic acid where in the ratio of a:b:c is n:(n+1):2, wherein n has a value from 1 to 20. The mixture of monomers is prepared in a 30 to 70 percent by weight solution of an organic solvent, a substrate impregnated with the solution and heated at 50 to 205 C to remove said solvent and form a low molecular weight prepolymer, and thereafter heated at 275 to 350 C to cure to a high molecular weight polyimide.

Serafini, T. T.↗