Oxygen isotopic compositions and oxygen concentrations of Apollo 14 and Apollo 15 rocks and soils.
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Clayton, R. N.↗
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Biomolecular budget of persistent, microbial-derived soil organic carbon: The importance of underexplored pools
The details of how soil microorganisms contribute to stable soil organic carbon pools are a pressing knowledge gap with direct implications for soil health and climate mitigation. It is now recognized that microbial necromass contributes substantially to the formation of stable soil carbon. However, the quantification of necromass in soils has largely been limited to model molecules such as aminosugar biomarkers. The abundance and chemical composition of other persistent microbial residues remain unresolved, particularly concerning how these pools may vary with microbial community structure, soil texture, and management practices. We use yearlong soil incubation experiments with an isotopic tracer to quantify the composition of persistent residues derived from microbial communities inhabiting sand or silt dominated soil with annual (corn) or perennial (switchgrass) monocultures. Persistent microbial residues were recovered in diverse soil biomolecular pools including metabolites, proteins, lipids, and mineral-associated organic matter (MAOM). The relative abundances of microbial contributions to necromass pools were consistent across cropping systems and soil textures. The greatest residue accumulation was not recovered in MAOM but in the light density fraction of soil debris that persisted after extraction by chemical fractionation using organic solvents. Necromass abundance was positively correlated with microbial biomass abundance and revealed a possible role of cell wall morphology in enhancing microbial carbon persistence; while gram-negative bacteria accounted for the greatest contribution to microbial-derived carbon by mass at one year, residues from gram-positive Actinobacteria and Firmicutes showed greater durability. Together these results offer a quantitative assessment of the relative importance of diverse molecular classes for generating durable soil carbon.
54 ENVIRONMENTAL SCIENCES↗
U-Th-Pb systematics of some Apollo 17 lunar samples and implications for a lunar basin excavation chronology
U, Th, and Pb concentrations and lead isotopic compositions of selected Apollo 17 soil and rock samples are presented. Concordia treatments of U-Pb whole samples of Apollo 17 mare basalts and highland rocks probably reflect several early thermal events about 4.5 b.y. old more consistently than do U-Pb ages of samples collected at other lunar sites. We propose that all lunar U-Th-Pb data reflect a multistate U-Pb evolution history most easily understood as being related to a complex planetesimal bombardment history of the moon which apparently dominated lunar events from about 4.5 to about 3.9 b.y. ago. Semi-distinct events at about 4.0, about 4.2, and 4.4-4.5 b.y. are evident on whole-rock frequency versus Pb-207/Pb-206 age histograms. Each of these events may reflect multiple cratering episodes. For mare basalts, complete resetting of the source rock U-Pb systems owing to Pb loss relative to U was apparently often approached after a major planetesimal impact.
Nunes, P. D.↗
Accumulation and isotopic evolution of carbon on the lunar surface
The processes of hydrogen stripping, agglutination and impact comminution, acting upon a regolith containing both indigenous and solar wind-implanted carbon, provide a quantitative explanation for the relationship between carbon abundance and isotopic composition observed for Apollo 16 soils.
Kerridge, J. F.↗
Diploptene: an indicator of terrigenous organic carbon in Washington coastal sediments
The pentacyclic triterpene 17 beta(H),21 beta(H)-hop-22(29)-ene (diploptene) occurs in sediments throughout the Columbia River drainage basin and off the southern coast of Washington state in concentrations comparable to long-chain plantwax n-alkanes. The same relationship is evident for diploptene and long-chain n-alkanes in soils from the Willamette Valley. Microorganisms indigenous to soils and soil erosion are indicated as the biological source and physical process, respectively, for diploptene in coastal sediments. Similarity between the stable carbon isotopic composition (delta 13CPDB) of diploptene isolated from soil in the Willamette Valley (-31.2 +/- 0.3%) and from sediments deposited throughout the Washington coastal environment (-31.2 +/- 0.5%) supports this argument. Values of delta for diploptene in river sediments are variable and 8-17% lighter, indicating that an additional biological source such as methane-oxidizing bacteria makes a significant contribution to the diploptene record in river sediments. Selective biodegradation resulting from a difference in the physicochemical association within eroded particles can explain the absence of the more-13C-depleted form of diploptene in Washington coastal sediments, but this mechanism remains unproven.
Non-NASA Center↗
Neutron capture effects in lunar gadolinium and the irradiation histories of some lunar rocks.
The Gd isotopic composition in 19 lunar rock and soil samples from three Apollo sites is reported. The analytical techniques and the high precision mass spectrometric measurements are discussed. Enrichments in the Gd-158 oxide to G-157 oxide ratio due to neutron capture range up to 0.75%. Integrated 'thermal' neutron fluxes derived from the isotopic anomalies of Gd are compared with spallation Kr data from aliquot samples to construct a model which gives both average cosmic-ray irradiation depths and effective neutron exposure ages for some rocks. Rock 14310 is the first lunar sample where Kr anomalies due to resonance neutron capture in Br are observed. A Kr-81/Kr exposure age of 262 (plus or minus 7)m.y. is calculated for this rock.
Lugmair, G. W.↗
The isotopic composition and concentration of water, hydrogen, and carbon in some Apollo 15 and 16 soils and in the Apollo 17 orange soil
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Epstein, S.↗
Nitrogen isotopes in drive tube 79002/79001 - Regolith history and nitrogen isotopic evolution in the solar wind
Variations in abundance and isotopic composition of nitrogen in 79002/79001 drive tube samples result from mixing of two soil components: one mature, N-rich, and isotopically light, resembling breccia material in the core, and the other immature, N-poor, and isotopically heavy. That these materials are common to soil at each stratigraphic level in the core suggests widespread distribution in the local regolith. Preservation of mixing correlations involving nitrogen isotopic compositions and cosmogenic N-15 concentrations suggests relatively recent mixing, perhaps in association with emplacement of the core stratigraphy. Characteristics of nitrogen release from the endmember materials, relationships between their nitrogen contents and maturity, and contrasts in their cosmogenic N-15 contents are consistent with models involving secular increase of the N-15/N-14 ratio of the solar wind.
Stone, J.↗
Nitrogen abundances and isotopic compositions in lunar samples
Isotopic analyses were carried out on soil separates as well as on bulk samples. Analyses of nitrogen fractions obtained by step-wise heating of the separates were also conducted. It was also attempted to obtain a value for the isotopic composition of indigenous lunar nitrogen from analyses of igneous rock samples. Several breccias were also analyzed for their nitrogen isotope ratios. The significance of the obtained results is discussed. Several lines of evidence point to the conclusion that the isotope ratio of the nitrogen being implanted into the lunar regolith has increased by some 15% over a period of at least 450 million years and possibly as long as 3,700 million years or more. This may be the result of changes in the nitrogen isotope ratio of the solar wind with time, or it may be due to outgassing and subsequent reimplantation of an isotopically light indigenous lunar nitrogen from the lunar interior in the early history of the moon.
Becker, R. H.↗
Lunar Science Conference, 6th, Houston, Tex., March 17-21, 1975, Proceedings. Volume 2 - Chemical and isotopic studies
The chemical compositions of lunar rocks and soils are examined, taking into account sulfur abundances and distributions in mare basalts and their source magmas, lithophile trace and major elements in Apollo 16 and 17 lunar samples, the role of vaporization processes in lunar rock formation, chemical studies of the lunar regolith with emphasis on zirconium and hafnium, a model for the lunar anorthositic gabbro, and trace-element chemistry and reducing capacity of size fractions from the Apollo 16 regolith. Other topics considered are related to lunar chronology, volatile meteoritic elements, isotopic studies, light element geochemistry, and agglutinates and regolith processes. Attention is given to meteoritic material in four terrestrial meteorite craters, the state of meteoritic material on the moon, volatile elements in Allende inclusions, oxygen isotope fractionation in Apollo 17 rocks, cosmogenic isotope production in Apollo deep-core samples, and the effects of exposure conditions on cosmic-ray records in lunar rocks.
Merrill, R. B.↗
A versatile system for biological and soil chemical tests on a planetary landing craft. I - Scientific objectives
We describe an approach for the remote detection and characterization of life in planetary soil samples. A mass spectrometer is used as the central sensor to monitor changes in the gas phase in eleven test cells filled with soil. Many biological assays, ranging from general 'in situ' assays to specific metabolic processes (such as photosynthesis, respiration, denitrification, etc.) can be performed by appropriate additions to the test cell via attached preloaded injector capsules. The system is also compatible with a number of chemical assays such as the analysis of atmospheric composition (both chemical and isotopic), the status of soil water, and the determination of compounds of carbon, nitrogen and sulfur in the soil.
Radmer, R. J.↗
A New Method for Evaluating the Carbon Isotope Characteristics of Carbonate Formed Under Cryogenic Conditions Analogous to Mars
The two upcoming robotic missions to Mars, Phoenix and MSL, will both have the capability of measuring the carbon isotopic composition of CO2 in the martian atmosphere, as well as possible CO2 trapped in carbonate minerals in the Martian soil. Results from orbital and landed missions now clearly indicate that no large scale deposits of carbonate materials exist at the surface. However, some results from orbital remote sensing have been interpreted to indicate that carbonate minerals are present as fine particles interspersed at low concentrations (approx. 2%) in the martian dust. One likely mechanism for the production of these carbonates is during the freezing of transient water near the surface. Large deposits of near surface ice and photographic evidence for flowing water on the surface suggest that transient melting and refreezing of H2O is an active process on Mars. Any exposure of these fluids to the CO2 rich atmosphere should al-low the production of HCO3- solutions. Carbonates are likely precipitates from these solutions during freezing as extensive CO2 degassing, driven by the fluid s decreasing volume, drives CO2 out. This rapid CO2 degassing increases the pH of the solution and drives carbonate precipitation. It has been shown in previous studies that this rapid CO2 degassing also results in a kinetic isotopic fractionation where the CO2 gas has a much lighter isotopic composition causing a large isotope enrichment of C-13 in the precipitated carbonate. This kinetic isotope enrichment may be very common in the current martian environment, and may be a very important factor in understanding the very high deltaC-13 values of carbonates found in the martian meteorites. However, while previous studies have succeeded in generally quantifying the magnitude of this effect, detailed studies of the consistency of this effect, and the freezing rates needed to produce it are needed to understand any carbon isotope analyses from carbonate minerals in the martian soil or dust. This study demonstrates an innovative new method for measuring the isotopic composition of gas evolved from the freezing of carbonate solutions in real time, which allows for a much clearer view of the chemical processes involved. This method now sets the stage for detailed analysis of the chemical and isotopic mechanisms that produce cryogenic carbonates.
Niles, P. B.↗
Mars Phoenix Scout Thermal Evolved Gas Analyzer (TEGA) Database: Thermal Database Development and Analysis
The Mars Phoenix Scout Lander mission in 2008 examined the history of water, searched for organics, and evaluated the potential for past/present microbial habitability in a martian arctic ice-rich soil [1]. The Thermal Evolved Gas Analyzer (TEGA) instrument measured the isotopic composition of atmospheric CO2 and detected volatile bearing mineralogy (perchlorate, carbonate, hydrated mineral phases) in the martian soil [2-7]. The TEGA data are archived at the Planetary Data System (PDS) Geosciences Node but are reported in forms that require further processing to be of use to the non-TEGA expert. The soil and blank TEGA thermal data are reported as duty cycle and must be converted to differential power (mW) to allow for enthalpy calculations of exothermic/endothermic transitions. The exothermic/endothermic temperatures are also used to determine what phases (inorganic/organic) are present in the sample. The objectives of this work are to: 1) Describe how interpretable thermal data can be created from TEGA data sets on the PDS and 2) Provide additional thermal data interpretation of two Phoenix soils (Baby Bear, Wicked Witch) and include interpretations from three unreported soils (Rosy Red 1, 2, and Burning Coals).
Sutter, B.↗
Lunar neutron stratigraphy.
Study of the isotopic composition of gadolinium and samarium in four soil and seven drill stem samples returned by the Apollo 15 mission. The results show the possibility to date sedimentary processes on the lunar surface for time scales of around 100 million years because of the particular dependence of neutron capture reactions on depth. The neutron flux has a distinct peak as a function of depth. This peak appears to lie below the level of shallow cratering for time scales of less than one billion years and consequently forms a readily identified marker layer of both depth and time.
Russ, G. P., III↗
Rubidium-strontium isotope characteristics of lunar soils.
Evaluation of K, Rb, and Sr concentrations and Sr isotopic composition for hand-picked fractions from the 175- to 1000-micron Apollo 12 fines samples 12032 and 12070 and for two less than 1-mm bulk fines samples, 14163,160 and 14259,21, from Apollo 14 which have model Rb-Sr ages close to 4.6 b.y. The Apollo 14 data indicate the presence of a radiogenic component of 4.6 b.y. model age like the Apollo 12 fines, confirming a very early geochemical differentiation of the moon. Progressively greater enrichment in K and Rb relative to the bulk fines is shown by microbreccia from both samples, ropy brown glass from 12032, and light-grey lithic fragments from 12032. Model Rb-Sr ages, based on a basaltic achondrite initial ratio, are generally close to 4.6 b.y. The microbreccias and ropy brown glass have model ages that are younger but indistinguishable from 4.6 b.y. within analytical error. Light grey lithic fragments from 12032 have a model age of 5.1 b.y. and must have had a multistage Rb/Sr evolution. The data are broadly compatible with two-component mixing models of the Apollo 12 fines. On the basis of modal composition, the microbreccia is considered the major nonbasaltic constituent.
Cliff, R. A.↗
Re-Os in Lunar Soils and Meteoritic Siderophiles on the Lunar Surface
Re-Os isotopes in lunar soils indicate approximately chondritic Re, Os, and Os isotopic compositions and substantial Re/Os fractionation, possibly due to the terminal lunar cataclysm. Additional information is contained in the original extended abstract.
Chen, J. H.↗
Depth of nutrient uptake by deep-rooted plants is regulated by water availability
The capacity of some plants to access water and nutrients at depths greater than one meter is a critical functional trait that confers resistance to drought and impacts both belowground and shallow soil processes. Here, we report water and strontium isotopic data from an alpine meadow transect showing the correlation between water and nutrient acquisition depths. The isotopic compositions of Sr ( 87 Sr/ 86 Sr ratio) and water in rock and soil, and in plant leaf tissues, reveal that deeper-rooted plants acquire a higher proportion of water, Sr, and cation nutrients that are derived from the saprolite, a zone of silicate weathering, than shallow-rooted grass. A three-decade dendrochemical record reveals that reductions of wet precipitation drive deep-rooted plants to acquire cation nutrients from deeper saprolite or bedrock regions. Thus, the depth of cation nutrient acquisition by deep-rooted plant species at this site is tightly coupled with, and likely determined by, water availability in soil, saprolite, and bedrock. The enhanced uptake of cations as well as water from deeper saprolite zones could impact the rate of bedrock weathering and watershed chemistry during drought.
biogeochemistry↗
Pb loss from Apollo 17 glassy samples and Apollo 16 revisited
U-Th-Pb analyses of bulk samples of soil breccia 70019, when compared to KREEP data, indicate that different lunar samples are sometimes characterized by distinctly different initial Pb isotopic compositions. U-Th-Pb analyses on nonglassy samples and a glassy separate of soil breccia 70019, and bulk and agglutinate samples of soil 72701 showed that the glassy samples did lose considerable Pb relative to U less than 200 million years ago. These data support the contention of other investigators that vaporization of volatile elements owing to impact events significantly alters the chemistry of the lunar regolith. Metaclastic rock 60315 was reanalyzed and was found to be concordant at 3.93 billion years rather than slightly discordant, as was previously reported.
Nunes, P. D.↗