Widespread occurrences of variably crystalline C-13-depleted graphitic carbon in banded iron formations

Almost all evidence for the oldest traces of life on Earth rely on particles of graphitic carbon preserved in rocks of sedimentary protolith. Yet, the source of carbon in such ancient graphite is debated, as it could possibly be non-biological and/or non-indigenous in origin. Here we describe the co-occurrence of poorly crystalline and crystalline varieties of graphitic carbon with apatite in ten different and variably metamorphosed banded iron formations (BIF) ranging in age from 1,800 to >3,800 Myr. In Neoarchean to Palaeoproterozoic BIF subjected to low-grade metamorphism, C-13-depleted graphitic carbon occurs as inclusions in apatite, and carbonate and arguably represents the remineralisation of syngenetic biomass. In BIF subjected to high-grade metamorphism, C-13-depleted graphite co-occurs with poorly crystalline graphite (PCG), as well as apatite, carbonate, pyrite, amphibole and greenalite. Retrograde minerals such as greenalite, and veins cross-cutting magnetite layers contain PCG. Crystalline graphite can occur with apatite and orthopyroxene, and sometimes it has PCG coatings. Crystalline graphite is interpreted to represent the metamorphosed product of syngenetic organic carbon deposited in BIF, while poorly crystalline graphite was precipitated from C-O-H fluids partially sourced from the syngenetic carbon, along with fluid-deposited apatite and carbonate. The isotopic signature of the graphitic carbon and the distribution of fluid-deposited graphite in highly metamorphosed BIF is consistent with carbon in the fluids being derived from the thermal cracking of syngenetic biomass deposited in BIF, but, extraneous sources of carbon cannot be ruled out as a source for PCG. The results here show that apatite + graphite is a common mineral assemblage in metamorphosed BIF. The mode of formation of this assemblage is, however, variable, which has important implications for the timing of life's emergence on Earth. (C) 2019 Elsevier B.V. All rights reserved.Peer reviewe

Geochemistry and petrogenesis of extension-related magmas close to the volcanic front of the Central part of the trans-mexican volcanic belt

New geochemical data for 23 samples from the Sierra de Chichinautzin (SCN) and Sierra Santa Catarina (SSC) located at the volcanic front of the central part of the Trans-Mexican Volcanic Belt were combined with the published data on 580 samples from the SCN to explore the origin and evolution of the Qua- ternary trachybasalt and basalt to andesite and dacite. The rare-earth element concentrations for the evolved intermediate and acid rocks are lower than those for the more basic varieties, implying that the evolved magmas cannot be generated by a simple fractional crystallisation process without crustal assimilation. The size of the Nb and Ta negative anomalies increases from basic to acid, which is similar to the behaviour of most continental rifts and extension-related areas, but contrasts from all island and continental arcs. The multidimensional tectonomagmatic diagrams indicate a continental rift setting from basic and alkaline intermediate magmas. The SSC represents a new site of within-plate alkaline magmas discovered in this work, which complements the earlier interpretation of the adjacent SCN as a manifestation of continental rift or extension-related magmatism

Abiotic anoxic iron oxidation, formation of Archean banded iron formations, and the oxidation of early Earth

Iron in the early anoxic oceans of Archean age (4000-2500 million years ago) is believed to have been oxidized to form banded iron formations (BIF). Previously, it has been proposed that iron was oxidized either by free oxygen, H2O2, microbial oxidation, or photo-oxidation. However, these mechanisms are difficult to reconcile with evidence for the oceans at that time having been largely devoid of dissolved oxygen and oxidants, together with the rarity of microbial remains in BIF and restrictively slow rates of photo-oxidation. Experiments reported here show that ferrous iron readily oxidizes in analogs of Archean anoxic seawater following the precipitation of ferrous hydroxide. Once precipitated, ferrous hydroxide undergoes decomposition to elemental iron that reacts with water at room temperature to form ferric iron and release hydrogen gas. The ferric iron may then be incorporated into green rust, a mixed ferrous-ferric phase that ages into iron minerals commonly found in BIF. Our finding suggests that anoxic iron oxidation may have contributed to the formation of oxide-facies BIF, especially Algoma-type BIF that likely formed in semi-restricted basins where ferrous hydroxide saturation was more easily achieved. Additionally, ferrous hydroxide decomposition would have contributed to early Earth's oxidation, as a result of hydrogen escape to space, thus providing new insights into environmental and biological conditions on early Earth