Refine
Document Type
- Article (3)
- Doctoral Thesis (1)
Language
- English (4)
Has Fulltext
- yes (4)
Is part of the Bibliography
- no (4)
Keywords
- Biogeochemistry (2)
- Biomineralization (1)
- Carbonate (1)
- Carbonated apatite (1)
- Clumped isotopes (1)
- Marine chemistry (1)
- Middle Miocene (1)
- Palaeoceanography (1)
- Palaeoclimate (1)
- Physical oceanography (1)
Institute
This Ph.D. thesis demonstrates i) the highly precise performance of refined and new analytical setups for clumped isotope analysis (Δ47 and Δ48) and ii) the applicability of clumped isotope analyses to biogenic and abiogenic carbonated apatite (Δ47) and abiogenic carbonates (Δ47 and Δ48) for research related to paleothermophysiology and paleoclimatology, whereas the overall analytical precision has been increased.
A comprehensive Δ47 dataset with 122 replicate analyses is provided from which the temperature dependence of Δ47 for (bio)apatite (Δ47-1/T2) is calculated between 1 °C and 80 °C. The temperature dependence of oxygen isotope equilibrium fractionation between carbonated synthetic apatite and water (1,000ln(αCHAP-H2O)) is experimentally determined. When applied to tooth enameloid from a modern Greenland shark (Somniosus microcephalus), a Late Miocene megatooth shark (Carcharodon megalodon), and an Upper Cretaceous Tyrannosaurus rex, reconstructed Δ47-based temperatures and δ18OH2O are in line with previously published data.
An analytical setup for highly precise clumped isotope analysis is described that allows for the simultaneous measurement of ∆47 and ∆48 in CO2 with external reproducibilities close to the respective shot-noise limits. The analyte gases originate from pure carbonates that were digested in hypersaturated orthophosphoric acid and purified using a fully automated device. Δ47 data sets with 117 replicate analyses in total on 22 pedogenic carbonate nodules from two Spanish Middle Miocene sections reveal the continental Southern European thermal structure during the end of the Middle Miocene Climatic Optimum (MCO) and the complete Middle Miocene Climatic Transition (MMCT; from 15.33 to 12.98 Ma).
Brachiopod shells are the most widely used geological archive for the reconstruction of the temperature and the oxygen isotope composition of Phanerozoic seawater. However, it is not conclusive whether brachiopods precipitate their shells in thermodynamic equilibrium. In this study, we investigated the potential impact of kinetic controls on the isotope composition of modern brachiopods by measuring the oxygen and clumped isotope compositions of their shells. Our results show that clumped and oxygen isotope compositions depart from thermodynamic equilibrium due to growth rate-induced kinetic effects. These departures are in line with incomplete hydration and hydroxylation of dissolved CO2. These findings imply that the determination of taxon-specific growth rates alongside clumped and bulk oxygen isotope analyses is essential to ensure accurate estimates of past ocean temperatures and seawater oxygen isotope compositions from brachiopods.
Abstract: Subaqueous carbonates from the Devils Hole caves (southwestern USA) provide a continuous Holocene to Pleistocene North American paleoclimate record. The accuracy of this record relies on two assumptions: That carbonates precipitated close to isotope equilibrium and that groundwater temperature did not change significantly in the last 570 thousand years. Here, we investigate these assumptions using dual clumped isotope thermometry. This method relies on simultaneous analyses of carbonate ∆47 and ∆48 values and provides information on the existence and extent of kinetic isotope fractionation. Our results confirm the hypothesis that calcite precipitation occurred close to oxygen and clumped isotope equilibrium during the last half million years in Devils Hole. In addition, we provide evidence that aquifer temperatures varied by less than ±1°C during this interval. Thus, the Devils Hole calcite δ18O time series exclusively represents changes in groundwater δ18O values. Plain Language Summary: The oxygen isotope composition of cave carbonates records changes in Earth's climate. However, the reliability of such records depends on how stable the carbonate precipitation environment was. Here, we use a novel method called dual clumped isotope thermometry that can provide simultaneous information on a carbonate's growth temperature and whether any additional fractionation processes affected its oxygen and clumped isotope signatures. Specifically, we investigated the Devils Hole caves, which provide a reference oxygen isotope time series for North America. We find that groundwater temperature did not change significantly in the last half-million years. Variations in the oxygen isotope composition of the deposited carbonates solely reflect variations in the oxygen isotope composition of the groundwater.
Surface temperature is a fundamental parameter of Earth’s climate. Its evolution through time is commonly reconstructed using the oxygen isotope and the clumped isotope compositions of carbonate archives. However, reaction kinetics involved in the precipitation of carbonates can introduce inaccuracies in the derived temperatures. Here, we show that dual clumped isotope analyses, i.e., simultaneous ∆47 and ∆48 measurements on the single carbonate phase, can identify the origin and quantify the extent of these kinetic biases. Our results verify theoretical predictions and evidence that the isotopic disequilibrium commonly observed in speleothems and scleractinian coral skeletons is inherited from the dissolved inorganic carbon pool of their parent solutions. Further, we show that dual clumped isotope thermometry can achieve reliable palaeotemperature reconstructions, devoid of kinetic bias. Analysis of a belemnite rostrum implies that it precipitated near isotopic equilibrium and confirms the warmer-than-present temperatures during the Early Cretaceous at southern high latitudes.