ALBERT

Description: Over the last two decades, popular opinion about prevailing conditions in the mid-Proterozoic deep ocean has evolved from fully oxygenated to globally euxinic (sulfidic) to a more heterogeneous, stratified water column with localized pockets of euxinia existing in predominantly iron-rich (ferruginous) deep waters. The Animikie Basin in theL ake Superior region has been essential in shaping our view of marine redox evolution over this time period. In this study, we present a multi-proxy paleoredox investigation of previously unanalyzed strata of the late Paleoproterozoic AnimikieB asin using drill cores through the -1.85 Ga Stambaugh Formation (PaintR iver Group) in the Iron River-Crystal Falls district of the Upper Peninsula of Michigan, USA. Based on previous tectonic reconstructions and analysis of sedimentary regimes, theI ronR iver-Crystal Falls section captures strata from among the deepest-water facies of the AnimikieB asin.I n contrast to previous work on sedimentary rocks in this basin, we find evidence from iron speciation, trace metal, and Mo isotope data for episodes of at least local deep-water oxygenation within a basin otherwise dominated by ferruginous and euxinic conditions. While tracemetal enrichments and iron speciation data suggest predominantly anoxic conditions, the occurrence of Mn-rich intervals (up to 12.3 wt% MnO) containing abundant Mn-Fe carbonate, and a wide range of Mo isotope data with extremely negative values (8 98195 Mo = -1.0 to + 1.1 %0), record the shuttling of Mn-oxides from surface waters through oxic or suboxic waters to the sediment-water interface. We propose that such conditions are analogous to those of locally restricted modern and Holocene basins in the Baltic Sea, which receive episodic inflow of oxygenated water, producing similar geochemical signatures to those observed for the AnimikieB asin. We argue that the mid-Proterozoic was characterized by a lack of a strong redox buffer (low sulfide, ferrous iron, and oxygen contents), and thus was vulnerable to dramatic, and at least local, redox shifts-including briefly oxygenated bottom waters. A refined view of the mid-Proterozoic ocean is emerging: one that was still predominantly anoxic, but marked by regional heterogeneities and short-term redox variability that may, in part, reflect a transitional state between prevailingly anoxic Archean and predominantly oxic Phanerozoic oceans.

Description: Iron formations (IF) represent an iron-rich rock type that typifies many Archaean and Proterozoic supracrustal successions and are chemical archives of Precambrian seawater chemistry and post-depositional iron cycling. Given that IF accumulated on the seafloor for over two billion years of Earth's early history, changes in their chemical, mineralogical, and isotopic compositions offer a unique glimpse into environmental changes that took place on the evolving Earth. Perhaps one of the most significant events was the transition from an anoxic planet to one where oxygen was persistently present within the marine water column and atmosphere. Linked to this progressive global oxygenation was the evolution of aerobic microbial metabolisms that fundamentally influenced continental weathering processes, the supply of nutrients to the oceans, and, ultimately, diversification of the biosphere and complex life forms. Many of the key recent innovations in understanding IF genesis are linked to geobiology, since biologically assisted Fe(II) oxidation, either directly through photoferrotrophy, or indirectly through oxygenic photosynthesis, provides a process for IF deposition from mineral precursors. The abundance and isotope composition of Fe(II)-bearing minerals in IF additionally suggests microbial Fe(III) reduction, a metabolism that is deeply rooted in the Archaea and Bacteria. Linkages among geobiology, hydrothermal systems, and deposition of IF have been traditionally overlooked, but now form a coherent model for this unique rock type. This paper reviews the defining features of IF and their distribution through the Neoarchaean and Palaeoproterozoic. This paper is an update of previous reviews by Bekker et al. (2010, 2014) that will improve the quantitative framework we use to interpret IF deposition. In this work, we also discuss how recent discoveries have provided new insights into the processes underpinning the global rise in atmospheric oxygen and the geochemical evolution of the oceans.

Description: The development and application of geochemical techniques to identify redox conditions in modern and ancient aquatic environments has intensified over recent years. Iron (Fe) speciation has emerged as one of the most widely used procedures to distinguish different redox regimes in both the water column and sediments, and is the main technique used to identify oxic, ferruginous (anoxic, Fe(II) containing) and euxinic (anoxic, sulfidic) water column conditions. However, an international sediment reference material has never been developed. This has led to concern over the consistency of results published by the many laboratories that now utilise the technique. Here, we report an interlaboratory comparison of four Fe speciation reference materials for palaeoredox analysis, which span a range of compositions and reflect deposition under different redox conditions. We provide an update of extraction techniques used in Fe speciation and assess the effects of both test portion mass, and the use of different analytical procedures, on the quantification of different Fe fractions in sedimentary rocks. While atomic absorption spectroscopy and inductively coupled plasma‐optical emission spectrometry produced comparable Fe measurements for all extraction stages, the use of ferrozine consistently underestimated Fe in the extraction step targeting mixed ferrous–ferric minerals such as magnetite. We therefore suggest that the use of ferrozine is discontinued for this Fe pool. Finally, we report the combined data of four independent Fe speciation laboratories to characterise the Fe speciation composition of the reference materials. These reference materials are available to the community to provide an essential validation of in‐house Fe speciation measurements.