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Abstract We investigate the origin and fate of lithogenic sediments using magnetic mineral assemblages in Barilari Bay, west Antarctic Peninsula (AP) from sediment cores recovered during the Larsen Ice Shelf System, Antarctica (LARISSA) NBP10‐01 cruise. To quantify and reconstruct Holocene changes in covarying magnetic mineral assemblages, we adopt an unsupervised mathematical unmixing strategy and apply it to measurements of magnetic susceptibility as a function of increasing temperature. Comparisons of the unmixed end‐members with magnetic observations of northwestern AP bedrock and the spatial distribution of magnetic mineral assemblages within the fjord, allow us to identify source regions, including signatures for “inner bay,” “outer bay,” and “northwestern AP” sources. We find strong evidence that supports the establishment of a late Holocene ice shelf in the fjord coeval with the Little Ice Age. Additionally, we present new evidence for late Holocene sensitivity to conditions akin to positive mean Southern Annual Mode states for western AP glaciers at their advanced Neoglacial positions. 

Abstract Two basalts with compositions relevant to the crusts of Mars and Earth were synthesized at igneous temperatures and held at 650°C for 21 to 257 days under quartz‐fayalite‐magnetitefO₂buffer conditions. The run products are germane to slowly cooled igneous intrusions, which might be a significant volumetric fraction of the Martian crust and carriers of magnetic anomalies in the Southern Highlands. Both basalts acquired intense thermoremanent magnetizations and intense but easily demagnetized anhysteretic remanent magnetizations carried by homogeneous multidomain titanomagnetite. Hypothetical intrusions on Mars composed of these materials would be capable of acquiring intense remanences sufficient to generate the observed anomalies. However, the remanence would be easily demagnetized by impact events after the cessation of the Mars geodynamo. Coercivity enhancement by pressure or formation of single domain regions via exsolution within the multidomain grains is necessary for long‐term retention of a remanence carried exclusively by multidomain titanomagnetite grains. 

Abstract We evaluate the relationship between the intensity of remanent magnetization andfO₂in natural and synthetic Mars meteorites. The olivine‐phyric shergottite meteorite Yamato 980459 (Y‐980459) and a sulfur‐free synthetic analog (Y‐98*) of identical major element composition were analyzed to explore the rock magnetic and remanence properties of a basalt crystallized from a primitive melt, and to explore the role of magmatic and alteration environmentfO₂on Mars crustal anomalies. The reducing conditions under which Y‐980459 is estimated to have formed (QFM‐2.5; Shearer et al. 2006) were replicated during the synthesis of Y‐98*. Y‐980459 contains pyrrhotite and chromite. Chromite is the only magnetic phase in Y‐98*. The remanence‐carrying capacity of Y‐980459 is comparable to other shergottites that formed in thefO₂range of QFM‐3 to QFM‐1. The remanence‐carrying capacity of these lowfO₂basalts is 1–2 orders of magnitude too weak to account for the intense crustal anomalies observed in Mars's southern cratered highlands. Moderately oxidizing conditions of >QFM‐1, which are more commonly observed in nakhlites and Noachian breccias, are key to generating either a primary igneous assemblage or secondary alteration assemblage capable of acquiring an intense remanent magnetization, regardless of the basalt character or thermal history. This suggests that if igneous rocks are responsible for the intensely magnetized crust, these oxidizing conditions must have existed in the magmatic plumbing systems of early Mars or must have existed in the crust during secondary processes that led to acquisition of a chemical remanent magnetization. 

The suevite (polymict melt rock-bearing breccia) composing the upper peak ring of the Chicxulub impact crater is extremely heterogeneous, containing a combination of relict clasts and secondary minerals. Using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM/EDS) and electron probe microanalysis (EPMA), we investigated the nature and occurrence of primary and secondary Fe-oxide and Fe-sulfide minerals to better understand hydrothermal trends such as mineral precipitation and dissolution, and to document the remobilization of Fe and associated siderophile elements within suevites. Large primary Fe-oxides (~20–100 µm) reveal decomposition and dissolution patterns, forming sub-micrometer to micrometer Fe-oxide phases. Secondary sub-micrometer Fe-oxide crystals are also visibly concentrated within clay. The occurrence of Fe-oxide crystals within clay suggests that these likely formed at temperatures ≤100 °C, near the formation temperature of smectite. The formation of Fe-oxide minerals on clay surfaces is of interest as it may form a micro-setting, where free electrons (from the oxidation of Fe2+) and the adsorption of simple organic molecules on the surface of clay could generate reactive conditions favorable to microbial communities. Primary and secondary Fe-sulfide minerals exhibiting a variety of morphologies are present within samples, representing different formation mechanisms. Secondary Fe-sulfide minerals occur within rims of clasts and vesicles and in fractures and voids. Some secondary Fe-sulfide grains are associated with Ni- and Co-rich phases, potentially reflecting the post-impact migration of siderophile elements within the suevite of the Chicxulub crater.