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The vast potential of using sediment adsorbed DNA as a window to past and present biodiversity rely on the ability of solid surfaces to adsorb environmental DNA. However, a comprehensive insight into DNA adsorption at surfaces in general is lacking. Soot and charcoal are carbonaceous materials widespread in the environment where they readily can come in contact with extracellular DNA shed from organisms. Using batch adsorption, we measured DNA adsorption capacity at soot and charcoal as a function of solution composition, time and DNA length. We observed that the adsorption capacity for DNA is highest at low pH, that it increases with solution concentration and cation valency and that the activation energy for DNA adsorption at both soot and charcoal is ~50 kJmol-1, suggesting strong binding. We demonstrate how the interaction between DNA and soot and charcoal partly occurs via terminal base pairs, suggesting that, besides electrostatic forces, hydrophobic interactions play an important role in binding. The large adsorption capacities and strong binding of DNA to soot and charcoal are features important for eDNA research and provide a motivation for use of carbonaceous materials from, e.g., anthropogenic pollution or wildfire as sources of biodiversity information.

In this study, the removal of benzotriazole (BTA), a pervasive aquatic contaminant widely used for its anti-corrosion, UV-stabilizing, and antioxidant properties, by nanomagnetite, biochar, and nanomagnetite–biochar composite is investigated. Nanomagnetite and nanomagnetite–biochar composite were synthesized under anoxic conditions and tested for BTA removal efficiency at neutral pH under both oxic and anoxic conditions at different time scales. Within the short time scale (up to 8 h), the removal of BTA by nanomagnetite–biochar composite was shown to be due to BTA deprotonation by the nanomagnetite surface. Through proton liberation, Fe²⁺ is released in accordance with the reaction Fe₃O₄ + 2H⁺ → Fe₂O₃ + Fe²⁺ + H₂O, which likely influences BTA complexation and its possible redox degradation. On the longer time scale, biochar achieved higher removal efficiency: 50% BTA removed within 48 h, due to formation of a ternary complex with surface Ca2+ ions, or 75% BTA removed after HCl biochar acid wash followed by Ca2+ surface saturation. As BTA presents significant environmental risks due to its extensive industrial applications, the present study offers critical insights into the mechanisms of BTA removal by nanomagnetite–biochar composite, and highlights the potential of such materials for water treatment applications. [ABSTRACT FROM AUTHOR]

Linking the timing of allanite growth to metamorphic conditions in metapelites is particularly challenging because of the large variety of allanite textures and chemical compositions. This study focuses on five garnet–biotite metapelites retrogressed to different extents, from the internal domain of the Longmen Shan (eastern Tibet) from which few petrochronological data documenting the metamorphic ages are available. Microstructural observations were combined with whole-rock compositions, detailed mineral characterization, phase equilibria modelling, and in situ U–Th/Pb allanite dating to gain insights into the allanite reactivity relative to other rock-forming minerals. All samples experienced similar peak temperatures of 560–600°C. Allanite is the main rare earth element (REE)-bearing accessory mineral but it exhibits different textures, such as epidote rims with distinct REE contents as well as late inclusion-like dissolution features. Garnet is, along with allanite, critical to reconstruct the REE budget of these rocks. In the two samples where allanite is observed as inclusions in garnet, garnet shows no textural zoning and a low Y content (<90 ppm). This is attributed to early Y fractionation in allanite and epidote rims with no further equilibration with garnet. This allanite is therefore pre-garnet (T  < 520°C). In the sample where allanite is observed only in the matrix, both garnet and allanite–epidote rims exhibit more complex textural and compositional zoning, with a higher Y content in garnet. The Y incorporation in garnet is attributed to a series of reactions involving allanite, interpreted as syn- to post-garnet growth (T  > 520°C). This relative chronology is confirmed by in situ U–Th/Pb allanite dating: pre-garnet allanite shows ages of c. 200 Ma, whereas syn- to post-garnet allanite has ages of c. 180 Ma. The timing of allanite appearance strongly correlates with the biotite-in reaction predicted by the models and observed in microstructures. In the two samples collected close to the major Wenchuan Shear Zone—deformed up to mylonitization and retrogressed under greenschist-facies conditions (3–4 ± 1 kbar, 350–400°C)—allanite still preserves the peak metamorphic ages (c. 200 and c. 180 Ma). Allanite and its epidote rims, however, are fragmented and partly replaced by a retrograde assemblage of Qz + Pb-depleted (<100 ppm) monazite, providing an age <90–100 Ma. Our results allow different metamorphic stages for the studied transect in the central Longmen Shan to be refined: a prograde path at c. 200 Ma, a thermal relaxation and exhumation from c. 180 Ma, and a late greenschist overprint. This study also shows that when allanite is the principal phase in a mineral assemblage datable by U–Th/Pb, detailed observations of allanite textures may be highly informative in constraining the timing of its growth relative to other major mineral phases. [ABSTRACT FROM AUTHOR]

Abstract: Linking ages to metamorphic stages in rocks that have experienced low‐ to medium‐grade metamorphism can be particularly tricky due to the rarity of index minerals and the preservation of mineral or compositional relicts. The timing of metamorphism and the Mesozoic exhumation of the metasedimentary units and crystalline basement that form the internal part of the Longmen Shan (eastern Tibet, Sichuan, China), are, for these reasons, still largely unconstrained, but crucial for understanding the regional tectonic evolution of eastern Tibet. In situ core‐rim 40Ar/39Ar biotite and U–Th/Pb allanite data show that amphibolite facies conditions (~10–11 kbar, 530°C to 6–7 kbar, 580°C) were reached at 210–180 Ma and that biotite records crystallization, rather than cooling, ages. These conditions are mainly recorded in the metasedimentary cover. The 40Ar/39Ar ages obtained from matrix muscovite that partially re‐equilibrated during the post peak‐P metamorphic history comprise a mixture of ages between that of early prograde muscovite relicts and the timing of late muscovite recrystallization at c. 140–120 Ma. This event marks a previously poorly documented greenschist facies metamorphic overprint. This latest stage is also recorded in the crystalline basement, and defines the timing of the greenschist overprint (7 ± 1 kbar, 370 ± 35°C). Numerical models of Ar diffusion show that the difference between 40Ar/39Ar biotite and muscovite ages cannot be explained by a slow and protracted cooling in an open system. The model and petrological results rather suggest that biotite and muscovite experienced different Ar retention and resetting histories. The Ar record in mica of the studied low‐ to medium‐grade rocks seems to be mainly controlled by dissolution–reprecipitation processes rather than by diffusive loss, and by different microstructural positions in the sample. Together, our data show that the metasedimentary cover was thickened and cooled independently from the basement prior to c. 140 Ma (with a relatively fast cooling at 4.5 ± 0.5°C/Ma between 185 and 140 Ma). Since the Lower Cretaceous, the metasedimentary cover and the crystalline basement experienced a coherent history during which both were partially exhumed. The Mesozoic history of the Eastern border of the Tibetan plateau is therefore complex and polyphase, and the basement was actively involved at least since the Early Cretaceous, changing our perspective on the contribution of the Cenozoic geology. [ABSTRACT FROM AUTHOR]

Alteration experiments on natural monazite crystals (Manangotry standard, Madagascar) under alkali conditions at 300, 400, 500 and 600 °C and 200 MPa were conducted to clarify mechanisms behind incomplete resetting of U-Th-Pb geochronological systems in monazite replaced by dissolution and precipitation processes. Above 400 °C, experimental products show typical replacement textures: a compositionally distinct monazite rim, referred as altered rim, surrounds the primary monazite (Mnz1). Isotopic and electron microprobe U-Th-Pb in situ dating of the altered rim yields intermediate ages between pristine monazite (555 Ma) and complete experimental resetting (0 Ma). Lead is systematically detected in altered rims, with concentration decreasing from 400 °C to 600 °C. The origin of incomplete resetting is elucidated with transmission electron microscope images that reveal an incomplete replacement of Mnz1 by a secondary monazite (Mnz2) within the altered rim. With increasing temperature, the size and volume of the Mnz2 within the altered rim become more important. Because no structural Pb or Pb nanoinclusions were observed, Pb in the altered rim is attributed to the Mnz1 component. Partial resetting of U-Th-Pb systems depends on the nanomixture of different Mnz1 proportions in the analyzed volume, and explains the higher rejuvenation at 600 °C than at lower temperatures. Although microanalytical techniques have the spatial resolution to date micrometer-sized rims, they are unable to resolve a nanoscale mixture of pristine and secondary monazite that could occur in altered rims formed by fluid-driven replacement, especially at low temperatures. Porosity and/or inclusions and complex age scattering in zoned monazite are significant markers that can indicate a possible nano-sized partial replacement. [ABSTRACT FROM AUTHOR]

Understanding the nature and preservation of microbial traces in extreme environments is crucial for reconstructing Earth's early biosphere and for the search for life on other planets or moons. At Rio Tinto, southwestern Spain, ferric oxide and sulfate deposits similar to those discovered at Meridiani Planum, Mars, entomb a diversity of fossilized organisms, despite chemical conditions commonly thought to be challenging for life and fossil preservation. Investigating this unique fossil microbiota can elucidate ancient extremophile communities and the preservation of biosignatures in acidic environments on Earth and, potentially, Mars. In this study, we use an innovative multiscale approach that combines the state-of-the-art synchrotron X-ray nanoimaging methods of ptychographic X-ray computed laminography and nano-X-ray fluorescence to reveal Rio Tinto's microfossils at subcellular resolution. The unprecedented nanoscale views of several different specimens within their geological and geochemical contexts reveal novel intricacies of preserved microbial communities. Different morphotypes, ecological interactions, and possible taxonomic affinities were inferred based on qualitative and quantitative 3D ultrastructural information, whereas diagenetic processes and metabolic affinities were inferred from complementary chemical information. Our integrated nano-to-microscale analytical approach revealed previously invisible microbial and mineral interactions, which complemented and filled a gap of spatial resolution in conventional methods. Ultimately, this study contributes to the challenge of deciphering the faint chemical and morphological biosignatures that can indicate life's presence on the early Earth and on distant worlds.