256 research outputs found

    Body temperatures of modern and extinct vertebrates from ^(13)C-^(18)O bond abundances in bioapatite

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    The stable isotope compositions of biologically precipitated apatite in bone, teeth, and scales are widely used to obtain information on the diet, behavior, and physiology of extinct organisms and to reconstruct past climate. Here we report the application of a new type of geochemical measurement to bioapatite, a “clumped-isotope” paleothermometer, based on the thermodynamically driven preference for ^(13)C and ^(18)O to bond with each other within carbonate ions in the bioapatite crystal lattice. This effect is dependent on temperature but, unlike conventional stable isotope paleothermometers, is independent from the isotopic composition of water from which the mineral formed. We show that the abundance of ^(13)C-^(18)O bonds in the carbonate component of tooth bioapatite from modern specimens decreases with increasing body temperature of the animal, following a relationship between isotope “clumping” and temperature that is statistically indistinguishable from inorganic calcite. This result is in agreement with a theoretical model of isotopic ordering in carbonate ion groups in apatite and calcite. This thermometer constrains body temperatures of bioapatite-producing organisms with an accuracy of 1–2 °C. Analyses of fossilized tooth enamel of both Pleistocene and Miocene age yielded temperatures within error of those derived from similar modern taxa. Clumped-isotope analysis of bioapatite represents a new approach in the study of the thermophysiology of extinct species, allowing the first direct measurement of their body temperatures. It will also open new avenues in the study of paleoclimate, as the measurement of clumped isotopes in phosphorites and fossils has the potential to reconstruct environmental temperatures

    Constraints on ocean circulation at the Paleocene–Eocene Thermal Maximum from neodymium isotopes

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    Global warming during the Paleocene-Eocene Thermal Maximum (PETM) ĝ1/4 ĝ€55 million years ago (Ma) coincided with a massive release of carbon to the ocean-atmosphere system, as indicated by carbon isotopic data. Previous studies have argued for a role of changing ocean circulation, possibly as a trigger or response to climatic changes. We use neodymium (Nd) isotopic data to reconstruct short high-resolution records of deep-water circulation across the PETM. These records are derived by reductively leaching sediments from seven globally distributed sites to reconstruct past deep-ocean circulation across the PETM. The Nd data for the leachates are interpreted to be consistent with previous studies that have used fish teeth Nd isotopes and benthic foraminiferal δ13C to constrain regions of convection. There is some evidence from combining Nd isotope and δ13C records that the three major ocean basins may not have had substantial exchanges of deep waters. If the isotopic data are interpreted within this framework, then the observed pattern may be explained if the strength of overturning in each basin varied distinctly over the PETM, resulting in differences in deep-water aging gradients between basins. Results are consistent with published interpretations from proxy data and model simulations that suggest modulation of overturning circulation had an important role for initiation and recovery of the ocean-atmosphere system associated with the PETM

    Determining the Diagenetic Conditions of Concretion Formation: Assessing Temperatures and Pore Waters Using Clumped Isotopes

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    Carbonate-δ^(18)O paleothermometry is used in many diagenetic studies to unravel the thermal history of basins. However, this approach generally requires an assumed pore-water δ^(18)O (δ^(18)O_(pw)) value, a parameter that is difficult to quantify in past regimes. In addition, many processes can change the original isotopic composition of pore water, which further complicates the assignment of an initial δ^(18)O_(pw) and can lead to erroneous temperature estimates. Here, we use clumped-isotope thermometry, a proxy based on the ^(13)C–^(18)O bond abundance in carbonate minerals, to evaluate the temperatures of concretion formation in the Miocene Monterey Formation and the Cretaceous Holz Shale, California. These temperatures are combined with established carbonate–water fractionation factors to calculate the associated δ^(18)O_(pw). Results demonstrate that diagenetic processes can modify the δ^(18)O of ancient pore water, confounding attempts to estimate diagenetic temperatures using standard approaches. Clumped-isotope-based temperature estimates for Monterey Formation concretions range from ∼ 17 to 35°C, up to ∼ 12°C higher than traditional δ^(18)O carbonate–water paleothermometry when δ^(18)O_(pw) values are assumed to equal Miocene seawater values. Calculated δ^(18)O_(pw) values range from +0.3 to +2.5‰ (VSMOW)—higher than coeval Miocene seawater, likely due to δ^(18)O_(pw) modification accompanying diagenesis of sedimentary siliceous phases. Clumped-isotope temperatures for the Holz Shale concretions range from ∼ 33 to 44°C, about 15 to 30°C lower than temperatures derived using the traditional method. Calculated δ^(18)O_(pw) values range from −5.0 to −2.9‰ and likely reflect the influx of meteoric fluids. We conclude that the use of clumped isotopes both improves the accuracy of temperature reconstructions and provides insight into the evolution of δ^(18)O_(pw) during diagenesis, addressing a longstanding conundrum in basin-evolution research

    Sensitivity of clumped isotope temperatures in fossil benthic and planktic foraminifera to diagenetic alteration

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    Applying the clumped isotope (Δ47) thermometer to foraminifer microfossils offers the potential to significantly improve paleoclimate reconstructions, owing to its insensitivity to the isotopic composition of seawater (unlike traditional oxygen isotope (δ18O) analyses). However, the extent to which primary Δ47 signatures of foraminiferal calcites can be overprinted during diagenesis is not well known. Here, we present Δ47 data as well as high-resolution (∼10 kyr) δ18O and δ13C middle Eocene time series, measured on benthic and planktic foraminifera from ODP/IODP Sites 1408, 1409, 1410, 1050, 1260 and 1263 in the Atlantic Ocean. The sites examined span various oceanographic regimes, including the western tropical to mid-latitude North Atlantic, and the eastern mid-latitude South Atlantic. Comparing data from contemporaneous foraminifera with different preservation states, we test the effects of diagenetic alteration on paleotemperature reconstructions for the deep and surface ocean. We find that overall, primary Δ47 signatures appear similarly sensitive to diagenetic overprinting as δ18O, with differences in sensitivity depending on pore fluid chemistry and the amount of secondary calcite. Where planktic foraminifera are significantly altered, sea surface temperatures derived from Δ47 and δ18O values are biased towards cool temperatures. In comparison, Δ47 and δ18O values of benthic and well preserved planktic foraminifera are less affected by diagenesis and thus likely to yield robust foraminiferal calcification temperatures. With independent estimates of diagenetic calcite fractions, secondary overprints could be corrected for, using end-member modeling and Δ47-based temperatures from benthic foraminifera

    Formation mechanisms of carbonate concretions of the Monterey Formation: Analyses of clumped isotopes, iron, sulfur and carbon

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    Carbonate concretions can form as a result of organic matter degradation within sediments. However, the ability to determine specific processes and formation temperatures of particular concretions has remained elusive. Here, we employ concentrations of carbonate-associated sulfate (CAS), δ^(34)S_(CAS) and clumped isotopes (along with more traditional approaches) to characterize the nature of concretion authigenesis within the Miocene Monterey Formation

    High regional climate sensitivity over continental China constrained by glacial-recent changes in temperature and the hydrological cycle

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    The East Asian monsoon is one of Earth’s most significant climatic phenomena, and numerous paleoclimate archives have revealed that it exhibits variations on orbital and suborbital time scales. Quantitative constraints on the climate changes associated with these past variations are limited, yet are needed to constrain sensitivity of the region to changes in greenhouse gas levels. Here, we show central China is a region that experienced a much larger temperature change since the Last Glacial Maximum than typically simulated by climate models. We applied clumped isotope thermometry to carbonates from the central Chinese Loess Plateau to reconstruct temperature and water isotope shifts from the Last Glacial Maximum to present. We find a summertime temperature change of 6–7 °C that is reproduced by climate model simulations presented here. Proxy data reveal evidence for a shift to lighter isotopic composition of meteoric waters in glacial times, which is also captured by our model. Analysis of model outputs suggests that glacial cooling over continental China is significantly amplified by the influence of stationary waves, which, in turn, are enhanced by continental ice sheets. These results not only support high regional climate sensitivity in Central China but highlight the fundamental role of planetary-scale atmospheric dynamics in the sensitivity of regional climates to continental glaciation, changing greenhouse gas levels, and insolation

    The role of temperature in the initiation of the end-Triassic mass extinction

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    International audienceThe end-Triassic mass extinction coincided with the eruption of the Central Atlantic Magmatic Province, a large igneous province responsible for the massive atmospheric input of potentially climate-altering volatile compounds that is associated with a sharp rise in atmospheric CO2. The extinction mechanism is debated, but both short-term cooling (similar to 10s of years) related to sulfur aerosols and longer-term warming (10,000 yrs) related to CO2 emissions-essentially opposite hypotheses-are suggested triggers. Until now, no temperature records spanning this crucial interval were available to provide a baseline or to differentiate between hypothesized mechanisms. Here, we use clumped-isotope paleothermometry of shallow marine microbialites coupled with climate modeling to reconstruct ocean temperature at the extinction horizon. We find mild to warm ocean temperatures during the extinction event and evidence for repeated temperature swings of similar to 16 degrees C, which we interpret as a signature of strong seasonality. These results constitute the oldest non-biomineralized marine seasonal temperature record. We resolve no apparent evidence for short-term cooling or initial warming across the 1-80kyr of the extinction event our record captures, implying that the initial onset of the biodiversity crisis may necessitate another mechanism

    A robust calibration of the clumped isotopes to temperature relationship for foraminifers

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    The clumped isotope (Δ47) proxy is a promising geochemical tool to reconstruct past ocean temperatures far back in time and in unknown settings, due to its unique thermodynamic basis that renders it independent from other environmental factors like seawater composition. Although previously hampered by large sample-size requirements, recent methodological advances have made the paleoceanographic application of Δ47 on small (<5 mg) foraminifer samples possible. Previous studies show a reasonable match between Δ47 calibrations based on synthetic carbonate and various species of planktonic foraminifers. However, studies performed before recent methodological advances were based on relatively few species and data treatment that is now outdated. To overcome these limitations and elucidate species-specific effects, we analyzed 14 species of planktonic foraminifers in sediment surface samples from 13 sites, covering a growth temperature range of ∼0–28 °C. We selected mixed layer-dwelling and deep-dwelling species from a wide range of ocean settings to evaluate the feasibility of temperature reconstructions for different water depths. Various techniques to estimate foraminifer calcification temperatures were tested in order to assess their effects on the calibration and to find the most suitable approach. Results from this study generally confirm previous findings that there are no species-specific effects on the Δ47-temperature relationship in planktonic foraminifers, with one possible exception. Various morphotypes of Globigerinoides ruber were found to often deviate from the general trend determined for planktonic foraminifers. Our data are in excellent agreement with a recent foraminifer calibration study that was performed with a different analytical setup, as well as with a calibration based exclusively on benthic foraminifers. A combined, methodologically homogenized dataset also reveals very good agreement with an inorganic calibration based on travertines. Our findings highlight the potential of the Δ47 paleothermometer to be applied to recent and extinct species alike to study surface ocean temperatures as well as thermocline variability for a multitude of settings and time scales

    The influence of temperature and seawater carbonate saturation state on 13C–18O bond ordering in bivalve mollusks

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    © The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 10 (2013): 4591-4606, doi:10.5194/bg-10-4591-2013.The shells of marine mollusks are widely used archives of past climate and ocean chemistry. Whilst the measurement of mollusk δ18O to develop records of past climate change is a commonly used approach, it has proven challenging to develop reliable independent paleothermometers that can be used to deconvolve the contributions of temperature and fluid composition on molluscan oxygen isotope compositions. Here we investigate the temperature dependence of 13C–18O bond abundance, denoted by the measured parameter Δ47, in shell carbonates of bivalve mollusks and assess its potential to be a useful paleothermometer. We report measurements on cultured specimens spanning a range in water temperatures of 5 to 25 °C, and field collected specimens spanning a range of −1 to 29 °C. In addition we investigate the potential influence of carbonate saturation state on bivalve stable isotope compositions by making measurements on both calcitic and aragonitic specimens that have been cultured in seawater that is either supersaturated or undersaturated with respect to aragonite. We find a robust relationship between Δ47 and growth temperature. We also find that the slope of a linear regression through all the Δ47 data for bivalves plotted against seawater temperature is significantly shallower than previously published inorganic and biogenic carbonate calibration studies produced in our laboratory and go on to discuss the possible sources of this difference. We find that changing seawater saturation state does not have significant effect on the Δ47 of bivalve shell carbonate in two taxa that we examined, and we do not observe significant differences between Δ47-temperature relationships between calcitic and aragonitic taxa.This work was funded by National Science Foundation grants ARC-1215551 to R. A. Eagle and A. K. Tripati, EAR-1024929 to R. A. Eagle and J. M. Eiler, and EAR-0949191 to A. K. Tripati. A. K. Tripati is also supported by the Hellman Fellowship program. Culture of bivalves in Kiel, Germany, was funded by the German Science Foundation (DFG Ei272/21-1, to Anton Eisenhauer) and the European Science Foundation (ESF) Collaborative Research Project CASIOPEIA (04 ECLIM FP08). Determination of bivalve mineralogy by J. B. Ries was funded by National Science Foundation grant OCE-1031995
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