We use d 18 O and d 13 C of oyster shells, inferred seawater d 18 O (d w ), and temperature tolerance ranges of modern zooxanthellate coral communities to constrain and model paleo-salinities of marginal-marine waters of the Miocene Lorca Basin, Spain. Salinities ranged from 22 to 32 PSU during growth of coral bioherms and carpets of the Soriana and Parrilla formations, and from 35 to 39 PSU during deposition of the Hondo Formation reef complex. The periods with lower modeled salinities correspond with deltaic and alluvial-fan sedimentation in the area. The modeling is supported by 87 Sr/ 86 Sr data and provides new insights into the evolution of the local depositional settings. Departures of Sr-isotope values from the global oceanic curve occur within the intervals with the lowest modeled salinities, and the non-oceanic 87 Sr/ 86 Sr preserved in individual oyster shells was probably sourced from uplifted Aquitanian-Burdigalian limestones. 87 Sr/ 86 Sr values that plot along the global ocean Sr-isotope curve for the late Miocene indicate a Tortonian age for the upper part of the Soriana Formation and the Parrilla Formation, and a Messinian age for the Hondo Formation. More generally, we demonstrate how the chemical analyses of oyster shells provide additional information regarding short-term oscillations of salinity and temperature of seawater beyond what can be obtained by traditional paleoecological methods.
Abstract. Insoluble particles in ice cores record signatures of past climate parameters like vegetation dynamics, volcanic activity, and aridity. For some of them, the analytical detection relies on intensive bench microscopy investigation and requires dedicated sample preparation steps. Both are laborious, require in-depth knowledge, and often restrict sampling strategies. To help overcome these limitations, we present a framework based on flow imaging microscopy coupled to a deep neural network for autonomous image classification of ice core particles. We train the network to classify seven commonly found classes, namely mineral dust, felsic and mafic (basaltic) volcanic ash grains (tephra), three species of pollen (Corylus avellana, Quercus robur, Quercus suber), and contamination particles that may be introduced onto the ice core surface during core handling operations. The trained network achieves 96.8 % classification accuracy at test time. We present the system's potential and its limitations with respect to the detection of mineral dust, pollen grains, and tephra shards, using both controlled materials and real ice core samples. The methodology requires little sample material, is non-destructive, fully reproducible, and does not require any sample preparation procedures. The presented framework can bolster research in the field by cutting down processing time, supporting human-operated microscopy, and further unlocking the paleoclimate potential of ice core records by providing the opportunity to identify an array of ice core particles. Suggestions for an improved system to be deployed within a continuous flow analysis workflow are also presented.
<p>Reconstructing the emergence and weathering of continental crust in the Archean is crucial for our understanding of early ocean chemistry, biosphere evolution and the onset of plate tectonics. However, considerable disagreement exists between the various elemental and isotopic proxies that have been used to trace crustal input into marine sediments, and data are scarce prior to 3 billion years ago. Here we show that chemical weathering modified the Sr isotopic composition of Archean seawater as recorded in 3.52 to 3.20 Ga stratiform marine-hydrothermal barite deposits from three different cratons. We use a combination of barite crystal morphology, oxygen, multiple sulfur and strontium isotope data to select barite samples with the most seawater-like isotopic compositions, and subsequently use these in a hydrothermal mixing model to calculate a plausible seawater Sr isotope evolution trend from measured <sup>87</sup>Sr/<sup>86</sup>Sr data. From modeled mixing ratios between seawater and hydrothermal fluids required for barite precipitation and comparison of <sup>87</sup>Sr/<sup>86</sup>Sr in theoretical seawater-hydrothermal fluid mixtures with those recorded in the barite, we obtain a novel seawater Sr isotope evolution trend for Paleoarchean seawater that is much more radiogenic than the curve previously determined from carbonate rocks. Our findings require the presence and weathering of subaerial and evolved (high Rb/Sr) crust from 3.7 &#177; 0.1 Ga onwards, and demonstrate that crustal weathering affected the chemistry of the oceans 500 million years earlier than previously thought.</p>
Reconstructing the emergence and weathering of continental crust in the Archean is crucial for our understanding of early ocean chemistry, biosphere evolution and the onset of plate tectonics. However, considerable disagreement exists between the elemental and isotopic proxies that have been used to trace crustal input into marine sediments and data are scarce prior to 3 billion years ago. Here we show that chemical weathering modified the Sr isotopic composition of seawater as recorded in 3.52-3.20 Ga stratiform barite deposits from three different cratons. Using a combination of Sr, S and O isotope data, barite petrography and a hydrothermal mixing model, we calculate a novel Sr isotope evolution trend for Paleoarchean seawater that is much more radiogenic than the curve previously determined from carbonate rocks. Our findings require the presence and weathering of subaerial and evolved (high Rb/Sr) crust from 3.7 ± 0.1 Ga onwards. This Eoarchean onset of crustal weathering affected the chemistry of the oceans and supplied nutrients to the marine biosphere 500 million years earlier than previously thought.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.