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.

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: R¹³_VPDB, R¹⁷_VSMOW, R¹⁸_VSMOW, 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.

Last glacial North Atlantic climate is characterized by abrupt, centennial‐millennial scale climate oscillations, called Dansgaard‐Oeschger (D‐O) events. Understanding the cause and propagation of these D‐O events into Eurasia is hampered by the scarcity of quantitative paleotemperature estimates from continental archives with precise, independent age models. Here, we present land snail shell carbonate clumped isotope‐based active season paleotemperature estimates and δ¹³C/δ¹⁸O‐based aridity reconstructions from Greenland stadial/interstadials (GS/GI) between 31 and 26.5 ka from the ¹⁴C‐dated Dunaszekcső loess section (Hungary). This reconstruction is complemented with a new ²³⁰Th‐dated flowstone stable isotope record covering 30‐26 ka. Our snail shell clumped isotope (Δ₄₇) data indicate growing season temperatures (GSTs) of 16°C–18°C and 7°C–14°C for the investigated interstadials and stadials, respectively. Stable carbon and oxygen stable isotope compositions of shells and flowstone calcite reveal milder interstadials with drier summers and more available moisture over the winter season, and colder stadials with annually/seasonally (winter) drier conditions, promoting increased loess/dust deposition. We propose that large‐scale ocean‐atmospheric variability, characterized by NAO phases, may have imparted a major control on transmitting abrupt North Atlantic climate event signals into continental Europe during the last glacial.

The tufa deposits in the Kurkur–Dungul area, southern Egypt, date from marine isotope stage (MIS) 11 to MIS 1. Springs across the region were active during glacial periods (with sea-level below –50 m), reflecting changed atmospheric circulation over the Indian Ocean, as well as peak interglacial periods. During times of low sea-level, reduced Indonesian throughflow promoted formation of an Indian Ocean Warm Pool, and anomalous rainfall on its western margin. We suggest that Egypt lies at the intersection of westerly (‘maghrebian’) and easterly (‘mashriqian’) rainfall provinces, which show different timing with relation to orbital forcing and different source water regions. Tufa-growth periods are therefore not mechanistically linked to ‘humid periods’ or ‘sapropel events’ identified elsewhere. Stable isotope and T (Δ ₄₇ ) data are also inconsistent with these spring systems being part of a larger system spanning northern Africa, and lack a clear interaction between northern hemisphere heating and mid-latitude rainfall. We also follow previous researchers in concluding that formation of springline deposit formation was probably delayed compared with rainfall, owing to aquifer flow distances. This delay is unlikely to be sufficient to explain why rainfall is out of phase with movements of the monsoon belts, but may complicate interpretation of these records. Supplementary material: A lithofacies description and supplementary figures and tables are available at https://doi.org/10.6084/m9.figshare.c.5246661

\ud Travertine is quite a common formation in the area of Budapest (Hungary) indicating strong hydrothermal activity during the Pliocene and Quaternary. It covers former terraces of the Danube River and older geomorphologic horizons; thus, it is an important archive to date fluvial terraces and tectonic movements. Despite numerous investigations performed on these deposits, only few radiometric data are available so far and the absence of the exact timing information hindered paleoclimatic interpretation. The area of Gellért Hill consists mainly of Upper Triassic dolomite, but Quaternary travertine can also be found. In this study a detailed petrographic and stable isotope geochemical study of four travertine sites (1. Ifjúsági Park; 2. Számadó u. (Street); 3. Kelenhegyi u. (Street); 4. Somlói u. (Street)) of the Gellért Hill area is presented, along with analyses on the recent carbonate deposits of Gellért Hill and Sárosfürdő. The travertine of Ifjúsági Park and Számadó u. are spring cone deposits, while the travertine of the Kelenhegyi u. represents a shallow-water depositional environment. Based on the paleontological studies of Jánossy (in Scheuer and Schweitzer, 1988) the Gellért Hill travertine was thought to have been formed during the Lower Pleistocene; however, no radiometric age dating had been performed on these deposits prior our study. Our U/Th analyses yielded ages of 250±44 ky for the Ifjúsági Park travertine (220 m asl) and 180±49 ky for the Számadó u. travertine (195 m asl). These new U/Th ages are in contradiction with the previously assumed Lower Pleistocene age, implying gradual relative decrease in the paleokarst water-level and proving that the elevation of the individual travertine deposits not necessarily show their relative age. The uplift rates of Gellért Hill calculated from the U/Th age data and elevation of travertine occurrences range between 0.47 and 0.52 mm/yr, which is significantly higher than the uplift rates calculated for the Rózsadomb area (0.20 0.25 mm/yr; Kele et al., submitted). The difference in the incision rates between the individual sub-areas suggests that selective uplift was characteristic for the Buda Hills during the Middle Pleistocene; thus, up-scaling reconstruction of paleokarst waterlevel for the whole area from a given locality is not possible.\ud Oxygen isotope analyses of recent carbonate deposits of Gellért Hill, Sárosfürdő and Rudas Spa revealed that these calcites precipitated under non-equilibrium conditions, and the measured calcitewater oxygen isotope fractionation show the same positive shift relative to “equilibrium values” as was observed in the case of the recently-forming Egerszalók travertine (Kele et al. 2008). Assuming that the water of the paleo-springs of Gellért Hill derived from precipitation infiltrated during interstadial periods of the Pleistocene and considering non-equilibrium deposition (i.e. using the empirical calcite-water oxygen isotope fractionation of Kele et al. 2008), their calculated paleotemperature could range between 22 (±4) °C and 49 (±6) °C. Based on the δ18Otravertine differences the Ifjúsági Park and the Számadó u. spring cone type travertine was deposited from the highest temperature water, while from the lowest temperature water the travertine of Kelenhegyi u. was formed.\u