Supernova versus Cosmic Ray Origin for Exotic Nuclides in Geomaterials: A Test Using 3He with 60Fe in Marine Sediments

David W. Graham, Kevin Konrad1
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2022.09.016]
College of Earth, Ocean, and Atmospheric Sciences, Oregon State University, Corvallis, OR 97331 USA
Copyright Elsevier

We report 3He and 4He concentrations in 57 sediment samples from the southeast Indian Ocean where 60Fe excesses were previously identified in a subset of the same samples (Wallner et al., 2016). The coupled 60Fe-3He data allow further evaluation of two competing hypotheses: 1) a nearby supernova (SN) showered Earth with exotic radionuclides such as 60Fe during the last 3 million years, or 2) 60Fe in terrestrial archives was generated by reactions of galactic cosmic rays (GCRs) on micrometeorite grains that were irradiated for hundreds of millions of years in the interstellar medium, where 3He production by GCRs is larger than the solar wind 3He flux.

Piston core ELT49-53 sediments show no correlation between 3He and 60Fe, and sedimentary 3He appears to be dominated by the presence of interplanetary dust particles (IDPs). Because 3He is not supplied in significant amounts by SN ejecta, the absence of a 3He-60Fe correlation provides additional, although circumstantial evidence for the supernova hypothesis. Large uncertainties in the relatively small number of sediment 60Fe measurements currently limit a firmer conclusion.

The extraterrestrial 3He accumulation rate in ELT49-53 from 3.2 to 1.7 Ma was 0.88±0.26×10-12 cm3 STP/g/kyr, similar to IDP 3He flux estimates from previous sedimentary and ice core records that span both shorter and longer time scales. 4He and 60Fe accumulation rates during this time interval were 0.11±0.04×10-6 cm3STP/cm2/kyr and 1.9±0.5×104 atoms/cm2/kyr. Bulk sediment [4He] is strongly anti-correlated with sediment CaCO3 content, evidence for modulation of the terrigenous and cosmic sedimentary fractions primarily by changes in biogenic carbonate deposition. Although the dominant terrigenous source has not been uniquely identified at the Indian Ocean deposition site, it resembles eolian material from the continental interior of Australia, and shows a narrow range of 3He/4He (from 2-4×10-8, 0.015-0.030 RA) over the last ∼3 Myrs.

Bulk compositions of the Chang’E-5 lunar soil: Insights into chemical homogeneity, exotic addition, and origin of landing site basalts

aKeqing Zong et al. (>10)
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2022.06.037]
1State Key Laboratory of Geological Processes and Mineral Resources, School of Earth Sciences, China University of Geosciences, Wuhan 430074, China
Copyright Elsevier

Lunar soil is a fine mixture of local rocks and exotic components. The bulk-rock chemical composition of the newly returned Chang’E-5 (CE-5) lunar soil was studied to understand its chemical homogeneity, exotic additions, and origin of landing site basalts. Concentrations of 48 major and trace elements, including many low-concentration volatile and siderophile elements, of two batches of the scooped CE-5 soil samples were simultaneously obtained by inductively coupled plasma mass spectrometry (ICP-MS) with minimal sample consumption. Their major and trace elemental compositions (except for Ni) are uniform at milligram levels (2–4 mg), matching measured compositions of basaltic glasses and estimates based on mineral modal abundances of basaltic fragments. This result indicates that the exotic highland and KREEP (K, rare earth elements, and P-rich) materials are very low (<5%) and the bulk chemical composition (except for Ni) of the CE-5 soil can be used to represent the underlying mare basalt. The elevated Ni concentrations reflect the addition of about 1 wt% meteoritic materials, which would not influence the other bulk composition except for some highly siderophile trace elements such as Ir. The CE-5 soil, which is overall the same as the underlying basalt in composition, displays low Mg# (34), high FeO (22.7 wt%), intermediate TiO2 (5.12 wt%), and high Th (5.14 µg/g) concentrations. The composition is distinct from basalts and soils returned by the Apollo and Luna missions, however, the depletion of volatile or siderophile elements such as K, Rb, Mo, and W in their mantle sources is comparable. The incompatible lithophile trace element concentrations (e.g., Ba, Rb, Th, U, Nb, Ta, Zr, Hf, and REE) of the CE-5 basalts are moderately high and their pattern mimics high-K KREEP. The pattern of these trace elements with K, Th, U, Nb, and Ta anomalies of the CE-5 basalts cannot be explained by the partial melting and crystallization of olivine, pyroxene, and plagioclase. Thus, the mantle source of the CE-5 landing site mare basalt could have contained KREEP components, likely as trapped interstitial melts. To reconcile these observations with the initial unradiogenic Sr and radiogenic Nd isotopic compositions of the CE-5 basalts, clinopyroxene characterized by low Rb/Sr and high Sm/Nd ratios could be one of the main minerals in the KREEP-bearing mantle source. Consequently, we propose that the CE-5 landing site mare basalts very likely originated from partial melting of a shallow and clinopyroxene-rich (relative to olivine and orthopyroxene) upper mantle cumulate with a small fraction (about 1–1.5 %) of KREEP-like materials.