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Paleosols represent fossil records of paleolandscape processes, paleobiotic interactions with the land surface, and paleoclimate. Paleosol-based reconstructions have figured prominently in the study of significant changes in global climate and terrestrial life, with one of the more highly studied examples being the end-Permian extinction (EPE). The EPE was once thought to consist of synchronous extinctions in the marine realm and the terrestrial realm, with the latter displaying a lower magnitude extinction of vertebrate, insect, and plant life. However, emerging stratigraphic records, anchored by high-precision U–Pb ages, and compilations of fossil taxa indicate that the terrestrial realm on Gondwana experienced an asynchronous extinction record with the marine realm; and, at the global-scale, possibly the lack of a true mass extinction for plant and vertebrate communities. Moreover, paleosol-based interpretations of the EPE on Gondwana typically focus on one depositional basin and extrapolate those finding to assess the potential for global paleoenvironmental/paleoclimatic change. This review compiles observations of paleosols, sedimentology, stratigraphy, and geochemical data across Gondwana during the Late Permian in order to critically assess these interpretations of global change in the lead up to the EPE. 

Phosphorus (P) is an essential limiting nutrient in marine and terrestrial ecosystems. Understanding the natural and anthropogenic influence on P concentration in soils is critical for predicting how its distribution in soils may shift as climate changes. While it is known that P is sourced from bedrock weathering, relationships between weathering, P, and other soil-forming factors have not been quantified at continental scales, limiting our ability to predict large-scale changes in P concentrations. Additionally, while we know that Fe oxide-associated P is an important P phase in terrestrial environments, the range in and controls on soil Fe concentrations and species (e.g., Fe in oxides, labile Fe) are poorly constrained. Here, we explore the relationships between soil P and Fe concentrations, soil order, climate, and vegetation in over 5000 soils, and Fe speciation in ca. 400 soils. Weathering intensity has a nuanced control on P concentrations in soils, with P concentrations peaking at intermediate weathering intensities (Chemical Index of Alteration, CIA~60). The presence of vegetation (but not plant functional types) affected soils’ ability to accumulate P. Contrary to expectations, P was not more strongly associated with Fe in oxides than other Fe phases. These results are useful both for predicting changes in potential P fluxes from soils to rivers under climate change and for reconstructing changes in terrestrial nutrient limitations in Earth’s past. In particular, soils’ tendency to accumulate more P with the presence of vegetation suggests that biogeochemical models invoking the evolution and spread of land plants as a driver for increased P fluxes in the geological record may need to be revisited. 

The geological record encodes the relationship between climate and atmospheric carbon dioxide (CO₂) over long and short timescales, as well as potential drivers of evolutionary transitions. However, reconstructing CO₂beyond direct measurements requires the use of paleoproxies and herein lies the challenge, as proxies differ in their assumptions, degree of understanding, and even reconstructed values. In this study, we critically evaluated, categorized, and integrated available proxies to create a high-fidelity and transparently constructed atmospheric CO₂record spanning the past 66 million years. This newly constructed record provides clearer evidence for higher Earth system sensitivity in the past and for the role of CO₂thresholds in biological and cryosphere evolution. 

Summary Plant carbon isotope discrimination is complex, and could be driven by climate, evolution and/or edaphic factors. We tested the climate drivers of carbon isotope discrimination in modern and historical plant chemistry, and focus in particular on the relationship between rising [CO₂] over Industrialization and carbon isotope discrimination.We generated temporal records of plant carbon isotopes from museum specimens collected over a climo‐sequence to test plant responses to climate and atmospheric change over the past 200 yr (includingPinus strobus,Platycladus orientalis,Populus tremuloides,Thuja koraiensis,Thuja occidentalis,Thuja plicata,Thuja standishiiandThuja sutchuenensis). We aggregated our results with a meta‐analysis of a wide range of C₃plants to make a comprehensive study of the distribution of carbon isotope discrimination and values among different plant types.We show that climate variables (e.g. mean annual precipitation, temperature and, key to this study, CO₂in the atmosphere) do not drive carbon isotope discrimination.Plant isotope discrimination is intrinsic to each taxon, and could link phylogenetic relationships and adaptation to climate quantitatively and over ecological to geological time scales. 

Abstract The sedimentary pyrite sulfur isotope (δ³⁴S) record is an archive of ancient microbial sulfur cycling and environmental conditions. Interpretations of pyrite δ³⁴S signatures in sediments deposited in microbial mat ecosystems are based on studies of modern microbial mat porewater sulfide δ³⁴S geochemistry. Pyrite δ³⁴S values often capture δ³⁴S signatures of porewater sulfide at the location of pyrite formation. However, microbial mats are dynamic environments in which biogeochemical cycling shifts vertically on diurnal cycles. Therefore, there is a need to study how the location of pyrite formation impacts pyrite δ³⁴S patterns in these dynamic systems. Here, we present diurnal porewater sulfide δ³⁴S trends and δ³⁴S values of pyrite and iron monosulfides from Middle Island Sinkhole, Lake Huron. The sediment–water interface of this sinkhole hosts a low‐oxygen cyanobacterial mat ecosystem, which serves as a useful location to explore preservation of sedimentary pyrite δ³⁴S signatures in early Earth environments. Porewater sulfide δ³⁴S values vary by up to ~25‰ throughout the day due to light‐driven changes in surface microbial community activity that propagate downwards, affecting porewater geochemistry as deep as 7.5 cm in the sediment. Progressive consumption of the sulfate reservoir drives δ³⁴S variability, instead of variations in average cell‐specific sulfate reduction rates and/or sulfide oxidation at different depths in the sediment. The δ³⁴S values of pyrite are similar to porewater sulfide δ³⁴S values near the mat surface. We suggest that oxidative sulfur cycling and other microbial activity promote pyrite formation in and immediately adjacent to the microbial mat and that iron geochemistry limits further pyrite formation with depth in the sediment. These results imply that primary δ³⁴S signatures of pyrite deposited in organic‐rich, iron‐poor microbial mat environments capture information about microbial sulfur cycling and environmental conditions at the mat surface and are only minimally affected by deeper sedimentary processes during early diagenesis.