• Energy Research

Chondritic meteorites can be appropriate substrates for the colonization of terrestrial microorganisms. However, determining whether organic compounds are intrinsic to the meteorite or come from external (terrestrial) contamination is still controversial. This research explores the molecular distribution and carbon isotopic composition of three lipid families (hydrocarbons, alkanoic acids, and alcohols) as well as DNA extracted from the interior of a CO carbonaceous chondrite named El Médano 464 (EM 464), discovered in the Atacama Desert in 2019. Three soil samples from the discovery area of EM 464 were collected and used as a background control for the composition and distribution of organic compounds. Our results revealed a higher abundance of the three lipid families in EM 464 compared with the surrounding soil samples. The organic compounds in EM 464 showed a mean δ13C value of -27.8 ± 0.5 for hydrocarbons (N = 20), -27.6 ± 1.1 for alkanoic acids (N = 17), and -27.5 ± 2.2‰ for alcohols (N = 18). These δ13C-depleted values are compatible with terrestrial biosignatures and are within isotopic values produced as a result of carbon fixation due to the Calvin cycle (δ13C of ca. from -19 to -34‰) widely used by photosynthetic terrestrial microorganisms. The DNA analysis (based on the bacterial 16S rRNA gene) showed a dominance of Proteobacteria (now Pseudomonadota) and Actinobacteriota in both meteorite and soils but exhibited different bacterial composition at the family level. This suggests that the microbial material inside the meteorite may have partially come from the adjacent soils, but we cannot rule out other sources, such as windborne microbes from distant locations. In addition, the meteorite showed higher bacterial diversity (H' = 2.4-2.8) compared with the three soil samples (H' = 0.3-1.8). Based on the distribution and δ13C value of organic compounds as well as DNA analysis, we suggest that most, if not all, of the organic compounds detected in the studied CO chondrite are of terrestrial origin (i.e., contamination). The terrestrial contamination of EM 464 by a diverse microbial community indicates that Atacama chondrites can offer distinctive ecological conditions for microorganisms to thrive in the harsh desert environment, which can result in an accumulation of microbial biomass and preservation of molecular fossils over time.

The future trajectory of greenhouse gas concentrations depends on interactions between climate and the biogeosphere. Thawing of Arctic permafrost could release significant amounts of carbon into the atmosphere in this century. Ancient Ice Complex deposits outcropping along the ~7,000-kilometre-long coastline of the East Siberian Arctic Shelf (ESAS), and associated shallow subsea permafrost, are two large pools of permafrost carbon, yet their vulnerabilities towards thawing and decomposition are largely unknown. Recent Arctic warming is stronger than has been predicted by several degrees, and is particularly pronounced over the coastal ESAS region. There is thus a pressing need to improve our understanding of the links between permafrost carbon and climate in this relatively inaccessible region. Here we show that extensive release of carbon from these Ice Complex deposits dominates (57 ± 2 per cent) the sedimentary carbon budget of the ESAS, the world’s largest continental shelf, overwhelming the marine and topsoil terrestrial components. Inverse modelling of the dual-carbon isotope composition of organic carbon accumulating in ESAS surface sediments, using Monte Carlo simulations to account for uncertainties, suggests that 44 ± 10 teragrams of old carbon is activated annually from Ice Complex permafrost, an order of magnitude more than has been suggested by previous studies. We estimate that about two-thirds (66 ± 16 per cent) of this old carbon escapes to the atmosphere as carbon dioxide, with the remainder being re-buried in shelf sediments. Thermal collapse and erosion of these carbon-rich Pleistocene coastline and seafloor deposits may accelerate with Arctic amplification of climate warming.