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Carbonates are ubiquitous in the rock record and provide a broad array of stable isotope-based paleoclimatic proxies (i.e., δ¹⁸O, δ¹³C, ∆¹⁷O, ∆₄₇, ∆₄₈) that provide information on stratigraphy, carbon cycling, temperature, hydrology, and the altitude of ancient land surfaces. Thus, carbonates are an essential archive of environmental and topographic histories of continental terranes. However, carbonate minerals are highly susceptible to post-depositional alteration of primary isotopic values via fluid-mediated and solid-state reactions. We propose a hierarchical suite of techniques to comprehensively assess alteration in carbonates, from essential and readily accessible tools to novel, high-resolution techniques. This framework provides a means of identifying preserved textures in differentially altered samples that contain high-value environmental information. To illustrate this progressive approach, we present a case study of Tethyan nearshore carbonates from the Paleocene Tso Jianding Group (Tibet). We demonstrate the utility of each technique in identifying chemical and crystallographic indicators of post-depositional alteration at progressively finer spatial scales. For example, secondary ionization mass spectrometry (SIMS) oxygen isotope maps of micrite and bioclasts reveal significant isotopic heterogeneity due to grain-scale water-rock exchange in textures that were labeled “primary” by optical inspection at coarser spatial resolution. Optical and cathodoluminescence microscopy should be the minimum required assessment of carbonate samples used in stable isotope analyses, but supplemented when necessary by SIMS, PIC mapping, and other yet untapped technologies that may allow distinction of primary and altered fabrics at finer spatial resolutions.

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.

We evaluate the efficacy of the stable isotope composition of precipitation and plant waxes as proxies for paleoaltimetry and paleohydrology in the northern tropical Andes. We report monthly hydrogen (δ²H_p) and oxygen (δ¹⁸O_p) isotope values of precipitation for an annual cycle, and hydrogen isotope values of plant waxes (δ²H_wax) obtained from modern soils along the eastern and western flanks of the Eastern Cordillera of Colombia. δ²H_p, δ¹⁸O_p, as well as the unweighted mean δ²H_waxvalues ofn‐C₂₉,n‐C₃₁, andn‐C₃₃n‐alkanes in the eastern flank show a dependence on elevation (R² = 0.90, 0.82, and 0.65, respectively). In stark contrast, the stable isotope compositions of neither precipitation nor plant waxes from the western flank correlate with elevation (R² < 0.23), on top of a negligible (p‐value >0.05) correlation between δ²H_waxand δ²H_p. In general, δ²H_waxvalues along the eastern flank of the Eastern Cordillera seem to follow the trend of a simple Rayleigh distillation process that is consistent with studies elsewhere on the eastern side of the Andes in South America. Neither δ²H_pnor δ¹⁸O_p, and therefore δ²H_wax, offer reliable estimates of past elevations in the western flank, due perhaps to water vapor source mixing, evaporation overprint, contrasting plant communities, and/or differences in evapotranspiration. Thus, δ²H_waxis only reliable for paleohydrology and paleoaltimetry reconstructions on the eastern flank of the Andes, whereas interpretations based on δ²H_pand/or δ¹⁸O_pwest of the highest point of the Eastern Cordillera need to consider mixing of moisture sources in addition to precipitation amount.

Documenting the spatio‐temporal progression of deformation within fold‐thrust belts is critical for understanding orogen dynamics. In the North American Cordillera, the geometry, magnitude, and timing of contractional deformation across a broad region of Nevada known as the “Sevier hinterland” has been difficult to characterize due to minimal exposures of syn‐contractional sedimentary rocks and overprinting of Cenozoic extension. To address this, we present geologic mapping and U‐Pb zircon geochronology from three exposures of the Cretaceous Newark Canyon Formation (NCF) in central Nevada. In the Cortez Mountains, NCF deposition between ∼119 and 110 Ma is hypothesized to be related to generation of relief by thrusting/folding to the west. In the Fish Creek Range, NCF deposition between ∼130 and 100 Ma was related to motion on an east‐vergent thrust fault. In the Pancake Range, NCF deposition is bracketed between ∼129 and 66 Ma and post‐dated east‐vergent folding. We incorporate these timing constraints into a compilation of deformation timing in the Sevier hinterland. Late Jurassic (∼165 and 155 Ma) shortening, which is largely post‐dated shortening in the Luning‐Fencemaker thrust belt to the west and pre‐dated initial deformation in the Sevier fold‐thrust belt to the east, is interpreted to represent diffuse, low‐magnitude deformation that accompanied eastward propagation of the basal Cordilleran décollement. Cretaceous (∼130 and 75 Ma) hinterland shortening, which includes deformation associated with NCF deposition, was contemporaneous with shortening in the Sevier fold‐thrust belt. This is interpreted to represent long‐duration strain partitioning between the foreland and hinterland during continued coupling above the basal décollement and the progressive westward underthrusting of thick North American lower‐middle crust.

Organic and inorganic stable isotopes of lacustrine carbonate sediments are commonly used in reconstructions of ancient terrestrial ecosystems and environments. Microbial activity and local hydrological inputs can alter porewater chemistry (e.g., pH, alkalinity) and isotopic composition (e.g., δ¹⁸O_water, δ¹³C_DIC), which in turn has the potential to impact the stable isotopic compositions recorded and preserved in lithified carbonate. The fingerprint these syngenetic processes have on lacustrine carbonate facies is yet unknown, however, and thus, reconstructions based on stable isotopes may misinterpret diagenetic records as broader climate signals. Here, we characterize geochemical and stable isotopic variability of carbonate minerals, organic matter, and water within one modern lake that has known microbial influences (e.g., microbial mats and microbialite carbonate) and combine these data with the context provided by 16S rRNA amplicon sequencing community profiles. Specifically, we measure oxygen, carbon, and clumped isotopic compositions of carbonate sediments (δ¹⁸O_carb, δ¹³C_carb, ∆₄₇), as well as carbon isotopic compositions of bulk organic matter (δ¹³C_org) and dissolved inorganic carbon (DIC; δ¹³C_DIC) of lake and porewater in Great Salt Lake, Utah from five sites and three seasons. We find that facies equivalent to ooid grainstones provide time‐averaged records of lake chemistry that reflect minimal alteration by microbial activity, whereas microbialite, intraclasts, and carbonate mud show greater alteration by local microbial influence and hydrology. Further, we find at least one occurrence of ∆₄₇isotopic disequilibrium likely driven by local microbial metabolism during authigenic carbonate precipitation. The remainder of the carbonate materials (primarily ooids, grain coatings, mud, and intraclasts) yield clumped isotope temperatures (T(∆₄₇)), δ¹⁸O_carb, and calculated δ¹⁸O_waterin isotopic equilibrium with ambient water and temperature at the time and site of carbonate precipitation. Our findings suggest that it is possible and necessary to leverage diverse carbonate facies across one sedimentary horizon to reconstruct regional hydroclimate and evaporation–precipitation balance, as well as identify microbially mediated carbonate formation.