Carbonate clumped-isotope thermometry is a promising technique that has the potential to help decode the significance of the variability of both physical and geochemical compositions of ancient carbonate rocks. This study utilizes a 600-million-year record of marine carbonate rocks from the subsurface and surface of the Sultanate of Oman to explore how burial and exhumation affected the carbonate clumped-isotope thermometer. Samples span 6 km of burial depth, and include calcite and dolomite mineralogies and a range of carbonate rock textures. We find evidence for two broad patterns in the physical and geochemical behavior of carbonate rocks during burial. The first group of carbonates yield water d 18 O VSMOW compositions slightly enriched or equal to an expected ''ice-free'' seawater composition of-1.2% and display good to fair textural preservation suggesting that cementation and lithification occurred within tens of meters of the sediment-water interface. Temperatures from the second group sit on the present-day geotherm, yield highly enriched water d 18 O VSMOW compositions, and display fair to poor textural preservation. We find no evidence for solid-state reordering in paired analyses of calcites and dolomites. Our results contribute to a growing body of work that indicates that the seawater d 18 O VSMOW composition has not changed significantly over 600 Myr and was not-6% in the Ediacaran. INTRODUCTION Marine carbonate fossils and rocks provide one of the best integrated records of ocean chemistry through time. However, the geochemistry of carbonate rocks records a series of overprinting events. During burial, shells, mud, and grains that precipitated from seawater experience dissolution to varying degrees, cements precipitate from pore fluids replacing or lithifying original components, and vein-filling and voidfilling carbonate cements precipitate from deeper-burial fluids. All of these processes leave textural evidence as well as chemical signatures and provide insight into the history of ancient rocks. The chemical metric that has arguably come closest to resolving questions concerning the postdepositional diagenetic path of a given carbonate component is the d 18 O of the mineral (Urey 1947). The d 18 O of a given carbonate component is dependent on both temperature, which changes with burial depth, and the composition of the precipitating fluid, which can change as pore fluids evolve when carbonate minerals are dissolved and reprecipitated. The d 18 O of a bulk sample of carbonate rock then reflects all the primary and secondary events, and their respective temperature and fluid histories, that are recorded by the d 18 O of various carbonate components (Brand 2004). This often-applied geochemical tool is imperfect in practice because it is impossible to deconvolve whether temperature and/or fluid composition is responsible for the observed d 18 O of a lithified carbonate rock or a single carbonate component (Urey 1947). Carbonate clumped-isotope thermometry (D 47) can deconvolve the contribution of ...