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Conventional carbonate–water oxygen isotope thermometry and the more recently developed clumped isotope thermometer have been widely used for the reconstruction of paleotemperatures from a variety of carbonate materials. In spite of a large number of studies, however, there are still large uncertainties in both δ 18 O- and Δ 47 -based temperature calibrations. For this reason there is a need to better understand the controls on isotope fractionation especially on natural carbonates. In this study we analyzed oxygen, carbon and clumped isotopes of a unique set of modern calcitic and aragonitic travertines, tufa and cave deposits from natural springs and wells. Together these samples cover a temperature range from 6 to 95 °C. Travertine samples were collected close to the vents of the springs and from pools, and tufa samples were collected from karstic creeks and a cave. The majority of our vent and pool travertines and tufa samples show a carbonate–water oxygen isotope fractionation comparable to the one of Tremaine et al. (2011) with some samples showing higher fractionations. No significant difference between the calcite–water and aragonite–water oxygen isotope fractionation could be observed. The Δ 47 data from the travertines show a strong relationship with temperature and define the regression Δ 47 = (0.044 ± 0.005 × 10 6 )/ T 2 + (0.205 ± 0.047). The pH of the parent solution, mineralogy and precipitation rate do not appear to significantly affect the Δ 47 -signature of carbonates, compared to the temperature effect and the analytical error. The tufa samples and three biogenic calcites show an excellent fit with the travertine calibration, indicating that this regression can be used for other carbonates as well. This work extends the calibration range of the clumped isotope thermometer to travertine and tufa deposits in the temperature range from 6 °C to 95 °C. [ABSTRACT FROM AUTHOR]