The start of the Palaeocene/Eocene thermal maximum--a period of exceptional global warming about 55 million years ago--is marked by a prominent negative carbon isotope excursion that reflects a massive input of 13C-depleted ('light') carbon to the ocean-atmosphere system. It is often assumed that this carbon injection initiated the rapid increase in global surface temperatures and environmental change that characterize the climate perturbation, but the exact sequence of events remains uncertain. Here we present chemical and biotic records of environmental change across the Palaeocene/Eocene boundary from two sediment sections in New Jersey that have high sediment accumulation rates. We show that the onsets of environmental change (as recorded by the abundant occurrence ('acme') of the dinoflagellate cyst Apectodinium) and of surface-ocean warming (as evidenced by the palaeothermometer TEX86) preceded the light carbon injection by several thousand years. The onset of the Apectodinium acme also precedes the carbon isotope excursion in sections from the southwest Pacific Ocean and the North Sea, indicating that the early onset of environmental change was not confined to the New Jersey shelf. The lag of approximately 3,000 years between the onset of warming in New Jersey shelf waters and the carbon isotope excursion is consistent with the hypothesis that bottom water warming caused the injection of 13C-depleted carbon by triggering the dissociation of submarine methane hydrates, but the cause of the early warming remains uncertain.

The clumped isotopic composition of carbonate‐derived CO2 (denoted Δ47) is a function of carbonate formation temperature and in natural samples can act as a recorder of paleoclimate, burial, or diagenetic conditions. The absolute abundance of heavy isotopes in the universal standards VPDB and VSMOW (defined by four parameters: R13VPDB, R17VSMOW, R18VSMOW, and λ) impact calculated Δ47 values. Here, we investigate whether use of updated and more accurate values for these parameters can remove observed interlaboratory differences in the measured T‐Δ47 relationship. Using the updated parameters, we reprocess 14 published calibration data sets measured in 11 different laboratories, representing many mineralogies, bulk compositions, sample types, reaction temperatures, and sample preparation and analysis methods. Exploiting this large composite data set (n = 1,253 sample replicates), we investigate the possibility for a “universal” clumped isotope calibration. We find that applying updated parameters improves the T‐Δ47 relationship (reduces residuals) within most labs and improves overall agreement but does not eliminate all interlaboratory differences. We reaffirm earlier findings that different mineralogies do not require different calibration equations and that cleaning procedures, method of pressure baseline correction, and mass spectrometer type do not affect interlaboratory agreement. We also present new estimates of the temperature dependence of the acid digestion fractionation for Δ47 (Δ*25‐X), based on combining reprocessed data from four studies, and new theoretical equilibrium values to be used in calculation of the empirical transfer function. Overall, we have ruled out a number of possible causes of interlaboratory disagreement in the T‐Δ47 relationship, but many more remain to be investigated.

Temperature dependence of oxygen-and clumped isotope fractionation in carbonates: a study of travertines and tufas in the 6-95°C temperature range, Geochimica et Cosmochimica Acta (2015), doi: http://dx.doi.org/10.1016/j.gca. 2015.06.032 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. calibrations. For this reason there is a need to better understand the controls on isotope 25 fractionation especially on natural carbonates. In this study we analyzed oxygen, carbon and 26 clumped isotopes of a unique set of modern calcitic and aragonitic travertines, tufa and cave 27 deposits from natural springs and wells. Together these samples cover a temperature range 28 from 6 to 95°C. Travertine samples were collected close to the vents of the springs and from 29 pools, and tufa samples were collected from karstic creeks and a cave. The majority of our 30 vent and pool travertines and tufa samples show a carbonate-water oxygen isotope 31 fractionation comparable to the one of Tremaine et al. (2011)

The impacts of the Paleocene‐Eocene thermal maximum (PETM) (∼55 Ma), one of the most rapid and extreme warming events in Earth history, are well characterized in open marine and terrestrial environments but are less so on continental margins, a major carbon sink. Here, we present stable isotope, carbonate content, organic matter content, and C:N ratio records through the PETM from new outcrop sections in California and from cores previously drilled on the New Jersey margin. Foraminifer δ18O data suggest that midlatitude shelves warmed by a similar magnitude as the open ocean (5°C–8°C), while the carbon isotope excursion (CIE), recorded both in carbonate and organic matter δ13C records, is slightly larger (3.3–4.5‰) than documented in open ocean records. Sediment accumulation rates increase dramatically during the CIE in marked contrast to the open ocean sites. In parallel, mass accumulation rates of both organic and inorganic carbon also increased by an order of magnitude. The estimated total mass of accumulated carbon in excess of pre‐CIE rates suggests that continental margins, at least along North America, became carbon sinks during the CIE, mainly because of weathering feedbacks and rising sea level. This result is significant because it implies that the negative feedback role of carbon burial on continental margins was greater than previously recognized.

The potential for carbonate clumped isotope thermometry to independently constrain both the formation temperature of carbonate minerals and fluid oxygen isotope composition allows insight into long‐standing questions in the Earth sciences, but remaining discrepancies between calibration schemes hamper interpretation of temperature measurements. To address discrepancies between calibrations, we designed and analyzed a sample suite (41 total samples) with broad applicability across the geosciences, with an exceptionally wide range of formation temperatures, precipitation methods, and mineralogies. We see no statistically significant offset between sample types, although the comparison of calcite and dolomite remains inconclusive. When data are reduced identically, the regression defined by this study is nearly identical to that defined by four previous calibration studies that used carbonate‐based standardization; we combine these data to present a composite carbonate‐standardized regression equation. Agreement across a wide range of temperature and sample types demonstrates a unified, broadly applicable clumped isotope thermometer calibration.

[1] We reconstruct eustatic variations during the latest Paleocene and earliest Eocene ($58-52 Ma). Dinoflagellate cysts, grain size fractions, and organic biomarkers in marine sections at four sites from three continents indicate an increased distance to the coast during the Paleocene-Eocene thermal maximum (PETM). The same trend is recognized in published records from other sites around the world. Together, the data indicate a eustatic rise during the PETM, beginning 20 to 200 ka before the globally recorded negative carbon isotope excursion (CIE) at $55.5 Ma. Although correlations are tentative, we recognize other global transgressions during Chrons C25n and C24n. The latter may be associated with Eocene Thermal Maximum 2 ($53.5 Ma) or the ''X''-event ($52 Ma). These results suggest a link between global sea level and ''hyperthermal'' intervals, potentially because of the melting of small alpine ice sheets on Antarctica, thermal expansion of seawater, or both. However, the early onset of sea level rise relative to the CIE of the PETM suggests contributions from other mechanisms, perhaps decreasing ocean basin volume, on sea level rise.

The exclusive use of carbonate reference materials is a robust method for the standardization of clumped isotope measurements • Measurements using different acid temperatures, designs of preparation lines, and mass spectrometers are statistically indistinguishable • We propose new consensus values for a set of 7 carbonate reference materials and updated guidelines to report clumped isotope measurements

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