Vanadium isotopic composition in meteoritic and terrestrial matter.
V 50/V 51 abundance ratios in chondrite, terrestrial diabase standard W-1 and reagent V
Balsiger, H.↗
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Carbon-rich Chondritic Clast PV1 from the Plainview H-chondrite Regolith Formation from H3 Chondrite Material by Possible Cometary Impact
Chondritic clast PV1 from the Plainview H-chondrite regolith breccia is a subrounded, 5-mm diameter unequilibrated chondritic fragment that contains 13 wt% C occurring mainly within irregularly shaped 30-400-micron-size opaque patches. The clast formed from H3 chondrite material as indicated by the mean apparent chondrule diameter (310 micron vs. approximately 300 micron in H3 chondrites), the mean Mg-normalized refractory lithophile abundance ratio (1.00 +/- 0.09 XH), the previously determined 0-isotopic composition (Delta O-17 = 0.66% vs. 0.68 +/- 0.04%0 in H3 chondrites and 0.73 +/- 0.09% in H4-6 chondrites), the heterogeneous olivine compositions in grain cores (with a minimum range of Fal-19), and the presence of glass in some chondrules. Although the clast lacks the fine-grained, ferroan silicate matrix material present in type 3 ordinary chondrites, PV1 contains objects that appear to be recrystallized clumps of matrix material. Similarly, the apparent dearth of radial pyroxene and cryptocrystalline chondrules in PV1 is accounted for by the presence of some recrystallized fragments of these chondrule textural types. All of the chondrules in PV1 are interfused indicating that temperatures must have briefly reached approximately 1100C (the approximate solidus temperature of H-chondrite silicate). The most likely source of this heating was by an impact. Some metal was lost during impact heating as indicated by the moderately low abundance of metallic Fe-Ni in PV1 (approximately 14 wt%) compared to that in mean H chondrites (approximately 18 wt%). The carbon enrichment of the clast may have resulted from a second impact event, one involving a cometary projectile, possibly a Jupiter-family comet. As the clast cooled, it experienced hydrothermal alteration at low water/rock ratios as evidenced by the thick rims of ferroan olivine around low-FeO olivine cores. The C-rich chondritic clast was later incorporated into the H-chondrite parent-body regolith and extensively fractured and faulted.
Rubin, Alan E.↗
Nitrogen isotope systematics of two Apollo 12 soils
Soils 12023 and 12037 were analyzed for nitrogen by step-wise heating. Helium contents, Ar-40/Ar-36 ratios and spallation N-15 ages were determined in addition to nitrogen contents and isotopic compositions. The results for 12023 show it to be a typical lunar soil similar to many Apollo 16 and 17 soils in its nitrogen content and delta N-15 value, with a complex history. Soil 12037 appears to have had a simple, two-stage surface exposure history; one exposure occurring recently for about 10-20 m.y. and the other between about 3 to 4 b.y. ago. The delta N-15 value of nitrogen implanted in the earlier exposure was -125%. This nitrogen may reside in the minor components of 12037 such as the KREEP. If it should reside in the basaltic component of 12037, however, then the variation in the delta N-15 of implanted nitrogen with time probably has been more complex than previously considered.
Becker, R. H.↗
Radiogenic Ingrowth of 40CA from Decay of 40K Provides a Powerful Tracer for Understanding the Origins of Felsic Magmas
Over time high K/Ca continental crust produces a unique Ca isotopic reservoir, with measurable 40Ca excesses compared to Earth's mantle (ɛCa=0). Thus, values of ɛCai > 1 indicate a significant crustal contribution to a magma. Values of ɛCai (<1) indistinguishable from mantle Ca indicate that the Ca in those magmas is either directly from the mantle, or is from partial melting of newly formed crust. So, whereas 40Ca excesses clearly define crustal contributions, mantle-like 40Ca/44Ca ratios are not as definitive. Here we present Ca isotopic measurements of intermediate to felsic igneous rocks from the western United States, and two crustal xenoliths found within the Fish Canyon Tuff (FCT). The two crustal xenoliths found within the 28.2 Ma FCT of the southern Rocky Mountain volcanic field (SRMVF) yield ɛCa values of ~4 and ~7.5, respectively. The 40Ca excesses of these possible source rocks are due to long-term in situ 40K decay and suggest that they are Precambrian in age. However, the FCT (ɛCai ~0.3) is within uncertainty of the mantle 40Ca/44Ca. Together, these data indicate that little Precambrian crust was involved in the petrogenesis of the FCT. Nd isotopic analyses of the FCT imply that it was generated from 10- 75% of an enriched component, and the Ca isotopic data appear to restrict that component to newly formed lower crust, or enriched mantle. However, the Ca isotopic data do permit assimilation of some crust with low Ca/Nd; decreasing the 143Nd/144Nd without adding much excess 40Ca to the FCT. Several other large tuffs from the SRMVF and from Yellowstone have ɛCai indistinguishable from the mantle. However, a few large tuffs from the SRMVF show significant 40Ca excesses. These tuffs (Wall Mountain, Blue Mesa, and Grizzly Peak) are likely sourced from near, or within the Colorado Mineral Belt. New isotopic measurements of Mesozoic and Tertiary granites from across the northern Great Basin show a range of ɛCai from 0 to ~3. In these samples ɛCai is generally correlated with ɛSri and is broadly negatively correlated with ɛNdi. However, for granites with similar ɛNdi at a given general location ɛCai can vary significantly (1 to 2 epsilon units). In rocks where low ɛNdi could also be due to melting from enriched reservoirs in the mantle lithosphere, the combination of high ɛCai with low ɛNdi clearly identifies crustal melts.
Mills, Ryan D.↗
Petrogenesis of Challis volcanics from central and southwestern Idaho - Trace element and Pb isotopic evidence
An analysis of the lava flows and ash-flow tuffs in Idaho is conducted to determine the composition of the volcanics in terms of major and trace elements and Pb isotopic substances. Al2O3 is found to be low, MgO content is high, and the concentration of K2O is higher or equal to that of Na2O with respect to the lavas of mafic to intermediate composition. Trace elements and element ratios are compatible with the crustal component, and the Pb isotopic compositions suggest a lack of assimilation during crystallization. The evidence does not support the notion of a magma system related to subduction, and the data regarding Pb isotopes and trace elements point to a connection with the lithosphere. A model is proposed for the Challis volcanics in which they resulted from completely melting within the lithosphere and then extending during the late Mesozoic and early Cenozoic compression.
Norman, Marc D.↗
The University of California Iron Isotope Experiment
We suggest a novel technique for resolving neighboring isotopes of iron-group nuclei with abundance ratios as great as 20:1 over the energy range from about 360 to about 550 MeV/nucleon. The determination of mass is based on the proportionality between mass and range and the negligible magnitude of range straggling. A balloon-borne experiment based on this technique is described which uses active electronic counters to measure particle speed, trajectory, and charge, and a passive polycarbonate plastic stack to measure range.
Ahlen, S. P.↗
Cosmic ray measurements of light and medium nuclei using a new telescope
Three separate balloon flights provided with a new multielement cosmic ray telescope are used to collect data on the isotopic composition of cosmic rays of Z equals 3 to 10 in the energy range 150-450 MeV/nuc. The discussion covers Li, Be, B, C, N, and O. The data on Ne is a new finding that suggests a possible enhancement of Ne-22 in cosmic rays relative to the normally accepted universal abundances. Other data are presented which directly verify the expected geomagnetic cutoff effects on isotopes characterized by different charge-to-mass ratio.
Preszler, A. M.↗
Nuclear processes and accelerated particles in solar flares
Nuclear processes and particle acceleration in solar flares are discussed and the theory of gamma-ray and neutron production is reviewed. Gamma-ray, neutron, and charged-particle observations of solar flares are compared with predictions, and the implications of these comparisons for particle energy spectra, total numbers, anisotropies, electron-to-proton ratios, and acceleration mechanisms are considered. Elemental and isotopic abundances of the ambient gas derived from gamma-ray observations have also been compared to abundances obtained from observations of escaping accelerated particles and other sources.
Ramaty, R.↗
The 158 micrometer (CII) line: A measure of global star formation activity in galaxies
Some 158 micron (CII) fine structure line observations from a sample of fourteen gas rich galaxies are reported. These measurements confirm and generalize previous basic results that the (CII) line is bright amounting to approximately 0.1 to 1 percent of the Far Infra Red (FIR) luminosity of the nuclear regions of galaxies; the (CII) line is formed in the warm (temperature of the gas is greater than 200 K), dense (n sub H greater than 1000/cu cm) photodissociated gas at the interfaces between giant molecular clouds and ionized gas regions and is therefore associated with the molecular gas component in spiral galaxies; the (CII) line tracks the FIR continuum in a manner consistent with the PDR models; the integrated (CII) to isotope (12)CO (transition 1 to 0) line ratio is large (greater than or equal to 1000) in all galaxies studied, and is similarly large for galactic molecular clouds; the (CII) line is therefore energetically very important for the study of giant molecular clouds. Conclusions obtained from these results are given.
Stacey, G. J.↗
Peering Through a Martian Veil: ALHA84001 Sm-Nd Age Revisited
The ancient Martian orthopyroxenite ALH84001experienced a complex history of impact and aqueous alteration events. Here we summarize Sm-147-Nd-143 and Sm-146-Nd-142 analyses performed at JSC. Further, using REE data, we model the REE abundance pattern of the basaltic magma parental to ALH84001 cumulus orthopyroxene. We find the Sm-146-Nd-142 isotopic data to be consistent with isotopic evolution in material having the modeled Sm/Nd ratio from a time very close to the planet's formation to igneous crystallization of ALH84001 as inferred from the Sm-Nd studies.
Nyquist, Laurence E.↗
Recycling of Oceanic Lithosphere: Water, fO2 and Fe-isotope Constraints
Spinel peridotite and garnet pyroxenite xenoliths from Hawaii provide important clues about the composition of the oceanic lithosphere, and can be used to assess its contribution to mantle heterogeneity upon recycling. The peridotites have lower bulk H2O (approximately 70-114 ppm) than the MORB source, qualitatively consistent with melt depletion. The garnet pyroxenites (high pressure cumulates) have higher H2O (200-460 ppm, up to 550 ppm accounting for phlogopite) and low H2O/Ce ratios (less than 100). The peridotites have relatively light Fe-isotopes (delta Fe -57 = -0.34 to 0.13) that decrease with increasing depletion, while the pyroxenites are significantly heavier (delta Fe-57 up to 0.3). The observed xenolith, as well as MORB and OIB total Fe-isotope variability is larger that can be explained by existing melting models. The high H2O and low H2O/Ce ratios of pyroxenites are similar to estimates of EM-type OIB sources, while their heavy delta Fe-57 are similar to some Society and Cook-Austral basalts. Therefore, recycling of mineralogically enriched oceanic lithosphere (i.e. pyroxenites) may contribute to OIB sources and mantle heterogeneity. The Fe(3+)/Sigma systematics of these xenoliths also suggest that there might be lateral redox gradients within the lithosphere, between juxtaposed oxidized spinel peridotites (deltaFMQ = -0.7 to 1.6, at 15 kb) and more reduced pyroxenites (deltaFMQ = -2 to -0.4, at 20-25kb). Such mineralogically and compositionally imposed fO2 gradients may generate local redox melting due to changes in fluid speciation (e.g. reduced fluids from pyroxenite encountering more oxidized peridotite). Formation of such incipient, small degree melts could further contribute to metasomatic features seen in peridotites, mantle heterogeneity, as well as the low velocity and high electrical conductivity structures near the base of the lithosphere and upper mantle.
Bizmis, M.↗
Measurement of C-12, O-16, and Fe-56 charge changing cross sections in helium at high energy, comparison with cross sections in hydrogen, and application to cosmic-ray propagation
We present measurements of the spallation cross sections of carbon, oxygen, and iron in helium and hydrogen, at beam energies from 540 to 1600 MeV/nucleon, performed by exposing liquid helium, CH2, and C targets. Charge changing cross sections are reported for fragments down to Ne for Fe + alpha and Fe + p reactions, and down to B for O + alpha, O + p, C + alpha, and C + p reactions. Alpha- to p-induced cross section ratios (sigma(sub alpha)/sigma(sub p)) are determined at the same energy per nucleon. From these measurements an empirical formula for the (sigma(sub alpha)/sigma(sub p)) ratios is derived and is found in good agreement with available isotopic cross sections data from radioactivity and radiochemical techniques. These results are applied to the propagation of heavy charged cosmic rays in an interstellar medium with a helium to hydrogen abundance ratio of 0.10. It is shown that the Sc-Mn/Fe ratio prediction is decreased relative to the B/C ratio when compared to propagation calculations in a pure hydrogen interstellar medium.
Ferrando, P.↗
Isotopic Composition of Trapped and Cosmogenic Noble Gases in Several Martian Meteorites
Isotopic abundances of the noble gases were measured in the following Martian meteorites: two shock glass inclusions from EET79001, shock vein glass from Shergotty and Y793605, and whole rock samples of ALH84001 and QUE94201. These glass samples, when combined with literature data on a separate single glass inclusion from EET79001 and a glass vein from Zagami, permit examination of the isotopic composition of Ne, Ar, Kr, and Xe trapped from the Martian atmosphere in greater detail. The isotopic composition of Martian Ne, if actually present in these glasses, remains poorly defined. The Ar-40/Ar-36 ratio of Martian atmospheric Ar may be much less than the ratio measured by Viking and possibly as low as approx. 1900. The atmospheric Ar-36/Ar-38 ratio is less than or equal to 4.0. Martian atmospheric Kr appears to be enriched in lighter isotopes by approx. 0.4%/amu compared to both solar wind Kr and to the Martian composition previously reported. The Martian atmospheric Ar-36/Xe-132 and Kr-84/Xe-132 Xe elemental ratios are higher than those reported by Viking by factors of approx. 3.3 and approx. 2.5, respectively. Cosmogenic gases indicate space exposure ages of 13.9 +/- 1 Myr for ALH84001 and 2.7 +/- 0.6 Myr for QUE94201. Small amounts of Ne-21 produced by energetic solar protons may be present in QUE94201, but are not present in ALH84001 or Y793605. The space exposure age for Y793605 is 4.9 +/- 0.6 Myr and appears to be distinctly older than the ages for basaltic shergottites.
Garrison, Daniel H.↗
The solar wind as deduced from lunar samples
Lunar surface samples, which have been exposed to the solar wind, can be used to obtain information on the recent and past solar wind. Some of the more important conclusions reached are: The D/H ratio in the solar wind is smaller than 0.000003. The isotopic composition of C, Ar (except Ar-40), and Kr in the solar wind and on the earth are the same within approximately plus or minus 3%. Terrestrial Ne is enriched in the heavier isotopes relative to solar wind Ne. The average solar wind flux in the past was probably higher than at present. The average solar wind energy has varied in the past; however, no long time trend is apparent. Evidence for a secular decrease of the He-4/He-3 ratio with time exists.
Eberhardt, P.↗
Volatiles in High-K Lunar Basalts
Chlorine is an unusual isotopic system, being essentially unfractionated ((delta)Cl-37 approximately 0 per mille ) between bulk terrestrial samples and chondritic meteorites and yet showing large variations in lunar (approximately -4 to +81 per mille), martian, and vestan (HED) samples. Among lunar samples, the volatile-bearing mineral apatite (Ca5(PO4)3[F,Cl,OH]) has been studied for volatiles in K-, REE-, and P (KREEP), very high potassium (VHK), low-Ti and high-Ti basalts, as well as samples from the lunar highlands. These studies revealed a positive correlation between in-situ (delta)Cl-37 measurements and bulk incompatible trace elements (ITEs) and ratios. Such trends were interpreted to originate from Cl isotopic fractionation during the degassing of metal chlorides during or shortly after the differentiation of the Moon via a magma ocean. In this study, we investigate the volatile inventories of a group of samples for which new-era volatile data have yet to be reported - the high-K (greater than 2000 ppm bulk K2O), high-Ti, trace element-rich mare basalts. We used isotope imaging on the Cameca NanoSIMS 50L at JSC to obtain the Cl isotopic composition [((Cl-37/(35)Clsample/C-37l/(35)Clstandard)-1)×1000, to get a value in per thousand (per mille)] which ranges from approximately -2.7 +/- 2 per mille to +16.1 +/- 2 per mille (2sigma), as well as volatile abundances (F & Cl) of apatite in samples 10017, 10024 & 10049. Simply following prior models, as lunar rocks with high bulk-rock abundances of ITEs we might expect the high-K, high-Ti basalts to contain apatite characterized by heavily fractionated (delta)Cl-37 values, i.e., Cl obtained from mixing between unfractionated mantle Cl (approximately 0 per mille) and the urKREEP reservoir (possibly fractionated to greater than +25 per mille.). However, the data obtained for the studied samples do not conform to either the early degassing or mixing models. Existing petrogentic models for the origin of the high-K, high-Ti basalts do not include urKREEP assimilation into their LMO cumulate sources. Therefore, Cl in these basalts either originated from source region heterogeneity or through assimilation or metasomatism by volatile and incompatible trace element rich materials. The new data presented here could provide evidence for the existence of region(s) in the lunar interior that are ITE-enriched and contain Cl that does not share isotopic affinities with lunar urKREEP, possibly representing the composition of the purported 'neuKREEP'.
Barnes, Jessica J.↗
The Cl isotope composition and halogen contents of Apollo-return samples
Lunar mare basalts are depleted in F and Cl by approximately an order of magnitude relative to mid-ocean ridge basalts and contain two Cl-bearing components with elevated isotopic compositions relative to the bulk-Earth value of ∼0‰. The first is a watersoluble chloride constituting 65 ± 10% of total Cl with δ37Cl values averaging 3.0 ± 4.3‰. The second is structurally bound chloride with δ37Cl values averaging 7.3 ± 3.5‰. These high and distinctly different isotopic values are inconsistent with equilibrium fractionation processes and instead suggest early and extensive degassing of an isotopically light vapor. No relationship is observed between F/Cl ratios and δ37Cl values, which suggests that lunar halogen depletion largely resulted from the Moon-forming Giant Impact. The δ37Cl values of apatite are generally higher than the structurally bound Cl, and ubiquitously higher than the calculated bulk δ37Cl values of 4.1 ± 4.0‰. The apatite grains are not representative of the bulk rock, and instead record localized degassing during the final stages of lunar magma ocean (LMO) or later melt crystallization. The large variability in the δ37Cl values of apatite within individual thin sections further supports this conclusion. While urKREEP (primeval KREEP [potassium/rare-earth elements/phosphorus]) has been proposed to be the source of the Moon’s high Cl isotope values, the ferroan anorthosites (FANs) have the highest δ37Cl values and have a positive correlation with Cl content, and yet do not contain apatite, nor evidence of a KREEP component. The high δ37Cl values in this lithology are explained by the incorporation of a >30‰ HCl vapor from a highly evolved LMO.
The Moon↗
Sm-Nd isotopic evolution of chondrites
The Nd-143/Nd-144 and Sm-147/Nd-144 ratios measured in 5 chondrites and the Juvinas achondrite correlated with the variation of 4.2% in Sm-147/Nd-144. Most of the spread in the range of these ratios results from small heterogeneities in the chondrites and does not reflect the large-scale volumetric averages. A new set of self-consistent reference values were selected for the 'chrondritic uniform reservoir' (CHUR); the new Sm-147/Nd-144 value is 1.6% higher than the previous value assigned to CHUR using the Juvinas data of Lugmair (1975). The new CHUR curve indicates significant changes in model ages for lunar rocks and in the interpretation of early lunar chronology.
Jacobsen, S. B.↗
Strontium isotopic variations of Neoproterozoic seawater - Implications for crustal evolution
High-precision Sr isotopic data were obtained on carbonate samples from the Neoproterozoic Shaler Group, Victoria Island (Canada). Results indicate that, between ca. 790 and 850 Ma, the Sr-87/Sr-86 ratio of seawater varied betweeen 0.70676 and 0.70561, with the minimum value at about 830 Ma. A curve of the Sr-87/Sr-86 seawater ratio vs. age showed that the new data substantially improve the existing isotopic record of Sr in seawater for the period 790-850 Ma. The Sr isotopic system data were coupled with data for the Nd isotopic system to model changes in the seafloor spreading rates (hydrothermal flux) and the continental erosion for the period 500-900 Ma. Results indicate that hydrothermal flux reached a maximum value at ca. 830 Ma, while a maximum in erosion rate occurred at ca. 570 Ma. These peaks are considered to be related to the developments in the Pan-African and related orogenic events.
Asmerom, Yemane↗