Al depth profile in Apollo 15 drill core

Cosmic-ray-produced²⁶Al (t_1/2 = 7.05 × 10⁵ years) has been measured in the Apollo 15 long core (surface to 390 g/cm²—218 cm) for study of galactic cosmic ray production profiles, using accelerator mass spectrometry. The results are in general accord with non-destructive counting data obtained earlier, but systematically lower, and significantly higher precision. From this experiment the half-attenuation length for²⁶Al production can be calculated to be 122 g/cm² (150–400 g/cm² region) after normalizing the data to average chemical composition. The⁵³Mn (t_1/2 = 3.7 × 10⁶ years) production profile in deep cores was also compiled to date. The half-attenuation length for⁵³Mn production was calculated to be 123 g/cm² (150–400 g/cm² region).     

Be andCl depth profiles in an Apollo 15 drill core

Cosmic-ray-produced¹⁰Be (t_1/2 = 1.6 × 10⁶ years) and³⁶Cl (t_1/2 = 3.0 × 10⁵ years) have been measured in the Apollo 15 long core for study of galactic cosmic ray production profiles using tandem accelerator mass spectrometry. From these experiments, the half-attenuation length for¹⁰Be production and³⁶Cl production were calculated to be 120 g/cm² and 132 g/cm² (150–400 g/cm² region). The measured half-attenuation length for¹⁰Be is slightly longer than that predicted by the Reedy-Arnold theoretical model. The flatter and somewhat deeper maximum seen in the³⁶Cl profile compared to the¹⁰Be,²⁶Al and⁵³Mn profiles can be explained by production from secondary thermal neutrons on³⁵Cl.     

Noble gas isotopic abundances and noble metal concentrations in sediments from the Cretaceous-Tertiary boundary

Noble gases in four sediment samples from the Cretaceous-Tertiary boundary collected near Stevns in Denmark were investigated to test the possibility of the presence of noble gases indicative for meteorites. All samples were also analyzed for the noble metals Os and Ir and twelve other elements. The observed enrichments of³He,⁴He and of Ar, Kr, and Xe relative to atmospheric abundances can be explained without invoking the addition of extraterrestrial material. The ²⁰Ne/²²Ne ratio and the Kr and Xe isotopic compositions are identical with the isotopic ratios in the terrestrial atmosphere. In contrast, the high noble metal concentrations indicate the presence of material with elemental abundances similar to chondritic matter. Compared to noble metals the noble gases are less sensitive tracers of an admixture of extraterrestrial matter in sediments.     

Microanalysis of nitrogen isotope abundances: association of nitrogen with noble gas carriers in Allende

Current research efforts to explore and account for the distribution of nitrogen isotope abundances in the ancient and present-day solar wind and in meteorites often require measurement of nitrogen abundances and isotopic compositions in very small samples of rare extraterrestrial materials. Isotopic analysis of ～ 1 μg of N₂ is possible with modern techniques of dynamic mass spectrometry, but even this high sensitivity is a limiting factor for certain critical samples. We have utilized a statistically operated mass spectrometer coupled to an ultrahigh vacuum gas extraction and processing system to lower this limit by approximately four orders of magnitude. Quantities of N₂ ranging from ～ 100 ng to < 100 pg are measurable with permil to percent precision in isotope ratios. Nitrogen and all noble gases evolved during stepwise combustion of fine-grained matrix material separated from the Allende meteorite have been meausred simultaneously in a pilot experiment using this technique. Isotopically heavy H-Xe (CCF-Xe) and isotopically light N are co-sited in a carbonaceous carrier phase, supporting a nucleosynthetic origin for¹⁵N-depleted nitrogen in Allende. The great isotopic uniformity of trapped Ar in all carrier phases indicates that simple, physical mass fractionation in gravitational escape of volatiles from the primitive nebula cannot have played a significant role in generating the nitrogen compositions observed in solar system matter.     

Inert gases from Apollo 11 and Apollo 12 fines: Reversals in the trends of relative element abundances

On the basis of the⁴He/²⁰Ne ratios in feldspathic particles from Apollo 11, basaltic fragments from Apollo 11, and magnetic separates from Apollo 12 fines, one expects the former to have the highest, and the Apollo 12 material to have the lowest⁸⁴Kr/¹³²Xe ratios. This is not the case; the⁸⁴Kr/¹³²Xe ratios from sample 12070 are substantially greater than those from the feldspathic and basaltic fragments in 10084. The trend-reversal in the feldspathic particles could be due to the trapping of genuine primordial lunar Kr and Xe. The reversal in the Apollo 11 basaltic fragments might be due to periodicnear-quantitative loss of the lighter gases by impact heating, with the Apollo 11 fines containing a relatively large proportion of strongly heated fragments.     

Variation in noble gas isotopic composition of gas samples from the Aegean arc, Greece

In contrast to most other arcs with oceanic plate subduction, the Aegean arc is characterized by continent–continent subduction. Noble gas abundances and isotopic compositions of 45 gas samples have been determined from 6 volcanoes along the arc, 2 islands in the back-arc region and 7 sites in the surrounding areas. The ³He/⁴He ratios of the samples ranged from 0.027R_A to 6.2R_A (R_A denotes the atmospheric ³He/⁴He ratio of 1.4×10⁻⁶), demonstrating that even the maximum ³He/⁴He ratio in the region is significantly lower than the maximum ratios of most oceanic subduction systems, which are equal to the MORB value of 8±1 R_A. Regional variations in the ³He/⁴He ratio were observed both along and across the arc. The maximum ³He/⁴He ratio was obtained from Nisyros volcano located in the eastern end of the arc, and the ratio decreased westward possibly reflecting the difference in potential degree of crustal assimilation or the present magmatic activity in each volcano. Across the volcanic arc, the ³He/⁴He ratio decreased with an increasing distance from the arc front, reaching a low ratio of 0.063R_A in Macedonia, which suggested a major contribution of radiogenic helium derived from the continental crust. At Nisyros, a temporal increase in ³He/⁴He ratio due to ascending subsurface magma was observed after the seismic crisis of 1995–1998 and mantle neon was possibly detected. The maximum ³He/⁴He ratio (6.2R_A) in the Aegean region, which is significantly lower than the MORB value, is not probably due to crustal assimilation at shallow depth or addition of slab-derived helium to MORB-like mantle wedge, but inherent characteristics of the subcontinental lithospheric mantle (SCLM) beneath the Aegean arc.     

Particle track record in Apollo 15 deep core from 54 to 80 cm depths

Particle track measurements have been made in nearly 500 individual grains from 13 levels in the 54–80 cm depth range of the Apollo 15 deep core. They reveal a wide range of track densities at all depths and some systematic variations within layers, indicating that both predepositional mixing and subsequent layering are present and that separate sub-layers exist within larger regions where no sub-layers are visible. Minimum track densities are inferred to be useful measures of maximum residence times for undisturbed layers. Using the observed minimum track densities we conclude that the average deposition rate in this section of soil column was ≥ 0.4 cm/million years.     

Chemical compositions and petrogenetic relationships in Apollo 15 mare basalts

Complex patterns of spreading centers were formed in Mesozoic time during the breakup of Gondwanaland and the Pacific tectonic plate. The approximate locus of each breakup can be identified by paleomagnetism, paleogeography, and plate tectonics. Each coincides with the present location of similarly complex patterns of intense positive gravity anomalies produced by rising and divergent mantle convection. Apparently the convection caused the breakups and the location and intensity of the convective pattern have not changed since Mesozoic time.     

Major,minor and trace element abundances in samples from the Apollo 17 station 7 boulder: Implications for the origin of early lunar crustal rocks

Apollo 17 station 7 boulder consortia samples were analyzed for major and minor elements by a combined semimicro atomic absorption spectrophotometric and colorimetric procedure. Lithophile trace element abundances were determined by stable isotope dilution mass spectrometry. Three matrix types samples (77135, 77115, and 77075) were found to be KREEP-rich fragment-laden melts with analogues throughout the Apollo 17 landing site. Of the five clasts analyzed, at least one (77115,19, troctolite) is thought to be a cumulate; 77135, 77115, and 77075 are thought to have originated by impact fusion of material with similar composition. This original material may represent a partial melt of a parent material of the composition of an included, shocked norite breccia (77215).     

The abundances of zirconium and hafnium in the solar system

The concentrations of zirconium and hafnium have been determined in Orgueil, Murchison, Allende, Bruderheim and Alais by RNAA. The mean Zr/Hf weight ratio in the first four of these meteorites is 31.3 ± 2.2 indicating no major fractionation of Zr from Hf. Alais contains anomalously high amounts of many refractory lithophile elements, including Zr and Hf. Orgueil contains 3.1 ppm Zr and 0.11 ppm Hf, corresponding to 9.0 and 0.16 atoms, respectively, relative to 10⁶ Si atoms.     

Atmospheric noble gas signatures in deep Michigan Basin brines as indicators of a past thermal event

Atmospheric noble gases (e.g., ²²Ne, ³⁶Ar, ⁸⁴Kr, ¹³⁰Xe) in crustal fluids are only sensitive to subsurface physical processes. In particular, depletion of atmospheric noble gases in groundwater due to boiling and steam separation is indicative of the occurrence of a thermal event and can thus be used to trace the thermal history of stable tectonic regions. We present noble gas concentrations of 38 deep brines (~ 0.5–3.6 km) from the Michigan Basin. The atmospheric noble gas component shows a strong depletion pattern with respect to air saturated water. Depletion of lighter gases (²²Ne and ³⁶Ar) is stronger compared to the heavier ones (⁸⁴Kr and ¹³⁰Xe). To understand the mechanisms responsible for this overall atmospheric noble gas depletion, phase interaction models were tested. We show that this atmospheric noble gas depletion pattern is best explained by a model involving subsurface boiling and steam separation, and thus, consistent with the occurrence of a past thermal event of mantle origin as previously indicated by both high ⁴He/heat flux ratios and the presence of primordial mantle He and Ne signatures in the basin. Such a conceptual model is also consistent with the presence of past elevated temperatures in the Michigan Basin (e.g., ~ 80–260 °C) at shallow depths as suggested by previous thermal studies in the basin. We suggest that recent reactivation of the ancient mid-continent rift system underneath the Michigan Basin is likely responsible for the release of both heat and mantle noble gases into the basin via deep-seated faults and fracture zones. Relative enrichment of atmospheric Kr and Xe with respect to Ar is also observed, and is interpreted as reflecting the addition of sedimentary Kr and Xe from associated hydrocarbons, following the hydrothermal event. This study pioneers the use of atmospheric noble gases in subsurface fluids to trace the thermal history of stable tectonic regions.     

Noble gas elemental and isotopic abundances in deep-sea trenches in the western Pacific

Noble gas elemental and isotopic abundances were measured in seven deep-sea water samples from five different sampling sites in the Nankai Trough, the Japan Trench and the Kuril Trench. The samples were obtained by the manned submersible “Nautile”. Most of the sampling sites are associated with clam colonies and/or fluid venting. Excesses both in³He/⁴He ratio and He concentration are observed in a seawater sample collected a few kilometers off the clam colonies which were found at a depth of 3830 m at the mouth of the Tenryu Canyon. Concentrations of noble gases (Ne, Ar, Kr and Xe) in this sample show progressive depletion from Ne to Xe relative to those in 1°C air-saturated seawater, which can be attributed to mixing of hot water ( 15°C) with cold ambient water ( 1°C). Isotopic compositions of Ne, Ar, Kr and Xe in this sample are atmospheric. These observations may reflect venting of hot pore water around the Tenryu Canyon. All the other samples show a significant excess in concentration of all noble gases relative to 1°C air-saturated seawater and the isotopic compositions are atmospheric. This excess of noble gas concentrations may appear to be air contamination in the samples. However, results of hydrocarbon analyses of the Kaiko samples imply that such large amount of air contamination is improbable. Decomposition of gas hydrate in deep-sea sediments is a more likely explanation for the observed excess of noble gas concentration.     

Trapped solar wind He,Ne, and Ar and energetic He in Surveyor 3

The Apollo 12 mission brought back sections of the Surveyor 3 vehicle suitable for mass spectrometric studies of implanted solar wind and solar cosmic rays. Using this method, we have determined an average solar wind ⁴He flux of 6.1 × 10⁶ ions/cm² sec for the 31 months of exposure. We have also measured ⁴He/³He= 2700 ± 50;⁴He/²⁰Ne= 410 ± 30;²⁰Ne/²²Ne= 13.5 ± 0.2;²⁰Ne/³⁶Ar= 24.5 ± 2.5; and ³⁶Ar/³⁸Ar= 5.41 ± 0.20. These measurements provide solar wind values averaged over considerably longer periods of time than the Apollo Solar Wind Composition experiments and suggest that the short term SWC measurements during a period of high solar activity may not be a reliable measure of average solar wind composition.     

Meteoritic and non-meteoritic trace elements in Luna 16 samples

Two Luna 16 soils have been analyzed for Ag, Au, Bi, Br, Cd, Co, Cs, Cu, Ga, Ge, In, Ur, Ni, Rb, Re, Sb, Se, Te, Tl, and Zn. A meteoritic component similar to that in Apollo 11 and 12 soils seems to be present, corresponding to ∼1.5 to 2% Cl chondrites or equivalent. It probably consists largely of micrometeorites. Three elements show strong enrichments compared to Apollo 11 and 12 soils: Cd (5× to 200×), Ag (5× to 10×), and Bi (3×). Presumably these elements were brought in by Cd-Ag-Bi rich material, similar to that in Unit VI of Apollo core 12028.     

The abundances of3H and 14C in the solar wind

Tritium is measured as a function of depth in a Surveyor 3 sample. The upper limit for solar-wind-implanted tritium gives a³H/¹H limit for the solar wind of 1 × 10^?11. The temperature release patterns of¹⁴C from lunar soils are measured. The¹⁴C release patterns from surface soils differ from a trench bottom soil and gives evidence for the presence of¹⁴C in the solar wind with a¹⁴C/¹H ratio of approximately 4 × 10^?11. The implications of these radio nuclide abundances in the solar wind are discussed.     

Quantifying effects of deep and near‐surface chemical erosion on cosmogenic nuclides in soils,saprolite, and sediment

Cosmogenic nuclides in rock, soil, and sediment are routinely used to measure denudation rates of catchments and hillslopes. Although it has been shown that these measurements are prone to biases due to chemical erosion in regolith, most studies of cosmogenic nuclides have ignored this potential source of error. Here we quantify the extent to which overlooking effects of chemical erosion introduces bias in interpreting denudation rates from cosmogenic nuclides. We consider two end‐member effects: one due to weathering near the surface and the other due to weathering at depth. Near the surface, chemical erosion influences nuclide concentrations in host minerals by enriching (or depleting) them relative to other more (or less) soluble minerals. This increases (or decreases) their residence times relative to the regolith as a whole. At depth, where minerals are shielded from cosmic radiation, chemical erosion causes denudation without influencing cosmogenic nuclide buildup. If this effect is ignored, denudation rates inferred from cosmogenic nuclides will be too low. We derive a general expression, termed the ‘chemical erosion factor’, or CEF, which corrects for biases introduced by both deep and near‐surface chemical erosion in regolith. The CEF differs from the ‘quartz enrichment factor’ of previous work in that it can also be applied to relatively soluble minerals, such as olivine. Using data from diverse climatic settings, we calculate CEFs ranging from 1.03 to 1.87 for cosmogenic nuclides in quartz. This implies that ignoring chemical erosion can lead to errors of close to 100% in intensely weathered regolith. CEF is strongly correlated with mean annual precipitation across our sites, reflecting climatic influence on chemical weathering. Our results indicate that quantifying CEFs is crucial in cosmogenic nuclide studies of landscapes where chemical erosion accounts for a significant fraction of the overall denudation. Copyright © 2012 John Wiley & Sons, Ltd.     

He and Ne isotopes in oceanic crust: implications for noble gas recycling in the mantle

In an attempt to determine the helium and neon isotopic composition of the lower oceanic crust, we report new noble gas measurements on 11 million year old gabbros from Ocean Drilling Program site 735B in the Indian Ocean. The nine whole rock samples analyzed came from 20 to 500 m depth below the seafloor. Helium contents vary from 3.3×10⁻¹⁰ to 2.5×10⁻⁷ ccSTP/g by crushing and from 5.4×10⁻⁸ to 2.4×10⁻⁷ ccSTP/g by melting. ³He/⁴He ratios vary between 2.2 and 8.6 Ra by crushing and between 2.9 and 8.2 by melting. The highest R/Ra ratios are similar to the mean mid-ocean ridge basalt (MORB) ratio of 8±1. The lower values are attributed to radiogenic helium from in situ α-particle production during uranium and thorium decay. Neon isotopic ratios are similar to atmospheric ratios, reflecting a significant seawater circulation in the upper 500 m of exposed crust at this site. MORB-like neon, with elevated ²⁰Ne/²²Ne and ²¹Ne/²²Ne ratios, was found in some high temperature steps of heating experiments, but with very small anomalies compared to air. These first results from the lower oceanic crust indicate that subducted lower oceanic crust has an atmospheric ²⁰Ne/²²Ne ratio. Most of this neon must be removed during the subduction process, if the ocean crust is to be recirculated in the upper mantle, otherwise this atmospheric neon will overwhelm the upper mantle neon budget. Similarly, the high (U+Th)/³He ratio of these crustal gabbros will generate very radiogenic ⁴He/³He ratios on a 100 Ma time scale, so lower oceanic crust cannot be recycled into either MORB or oceanic island basalt without some form of processing.     

A komatiite component in Apollo 16 highland breccias: implications for the nickel-cobalt systematics and bulk composition of the moon

The lunar crust at the Apollo 16 landing site contains substantial amounts of a “primitive component” in which the ferromagnesian group of elements is concentrated. The composition of this component can be retrieved via an analysis of mixing relationships displayed by lunar breccias. It is found to be a komatiite which is compositionally similar to terrestrial komatiites both in major and minor elements. The komatiite component of the lunar crust is believed to have formed by extensive degrees of melting of the lunar interior at depths greater than were involved in the formation of the lunar magma ocean which was parental to the crust. After formation of the anorthositic crust, it was invaded by extensive flows and intrusions of komatiite magma from these deeper source regions. The komatiites became intimately mixed with the anorthosite by intensive meteoroid impacts about 4.5 b.y. ago, thereby accounting for the observed mixing relationships displayed by the crust. The compositional similarity between lunar and terrestrial komatiites strongly implies a corresponding similarity between the compositions of their source regions in the lunar interior and the Earth's upper mantle. The composition of the lunar interior can be modelled more specifically by combining the komatiite composition with its liquidus olivine composition (as determined experimentally) in proportions chosen so as to produce a cosmochemically acceptable range of Mg/Si ratios for the bulk Moon. Except for higher FeO and lower Na₂O, the range of compositions thereby obtained for the bulk moon is very similar to the composition of the Earth's upper mantle.The effects of meteoritic contamination on the abundances of cobalt and nickel in lunar highland breccias were subtracted on the assumption that the contaminating projectiles were chondritic. The cobalt and nickel residuals thereby obtained were found to correlate strongly with the (Mg + Fe) content of the breccias, demonstrating that the Co and Ni are associated with the ferromagnesian component of the breccias and are genuinely indigenous to the Moon. The lunar highland Co and Ni residuals also display striking Ni/Co versus Ni correlations which follow a similar trend to those displayed by terrestrial basalts, picrites and komatiites. The lunar trends provide further decisive evidence of the indigenous nature of the Co and Ni residuals and suggest the operation of extensive fractionation controlled by olivine-liquid equilibria in producing the primitive component of the lunar breccias. Indigenous nickel abundances at the Apollo 14, 15 and 17 sites are much lower than at the Apollo 16 site, although rocks from all sites follow the same Ni/Co versus Ni trends. It is suggested that the primitive component at the Apollo 14, 15 and 17 sites was generally of basaltic composition, in contrast to the komatiitic nature of the Apollo 16 primitive component.     

深层油气地球物理勘探基础研究

本文讨论当前我国深层油气地震勘探面临的难题及基础研究的三个主攻方向,包括：困难地区深层地震反射体准确成像,地震波场信息学、油气田直接预测的地球物理方法技术等.