The isotope composition of precipitation has been monitored in monthly precipitation at Zagreb, Croatia, since 1976. Here, we present a statistical analysis of available long-term isotope data (3H activity concentration, δ2H, δ18O, and deuterium excess) and compare them to basic meteorological data. The aim was to see whether isotope composition reflected observed climate changes in Zagreb: a significant increase in the annual air temperature and larger variations in the precipitation amount. Annual mean δ18O and δ2H values showed an increase of 0.017‰ and 0.14‰ per year, respectively, with larger differences in monthly mean values in the first half of the year than in the second half. Mean annual d-excess remained constant over the whole long-term period, with a tendency for monthly mean d-excess values to decrease in the first half of the year and increase in the second half due to the influence of air masses originating from the eastern Mediterranean. Changes in the stable isotope composition of precipitation thus resembled changes in the temperature, the circulation pattern of air masses, and the precipitation regime. A local meteoric water line was obtained using different regression methods, which did not result in significant differences between nonweighted and precipitation-weighted slope and intercept values. Deviations from the Global Meteoric Water Line GMWL (lower slopes and intercepts) were observed in two recent periods and could be explained by changes in climate parameters. The temperature gradient of δ18O was 0.33‰/°C. The tritium activity concentrations in precipitation showed slight decreases during the last two decades, and the mean A in the most recent period, 2012–2018, was 7.6 ± 0.8 Tritium Units (TU).

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Carbon isotope composition of dissolved inorganic carbon (DIC) was studied at springs, lakes and tributaries of the Plitvice Lakes. The Plitvice Lakes are a unique and complex karst lakes system consisting of 16 flow-through lakes connected by waterfalls and streams and characterized by intense calcium carbonate precipitation in the form of tufa and lake sediments. Two main springs have different 14C concentrations due to different geology and their variations were controlled by flow rates. Further downstream, at lakes to the Korana River that outflows from the lakes, the 14C activity and δ13C consistently increased down the flow. Carbon isotope composition from 2010 to 2015 was compared with the values measured 30 years earlier. The variation in δ13CDIC was accounted for seasonal change, while 14C activity of surface water DIC decreased 7–12% during the 30 years. Using a semi-empiric model, it is calculated that the downstream increase is controlled by the exchange of DIC and atmospheric CO2 carbon and by introduction of decomposed biogenic carbon from the top soil organic matter of the lakes surrounding area in almost equal proportions.

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Tufa is a fresh-water surface calcium carbonate deposit precipitated at or near ambient temperature, and commonly contains the remains of macro- and microphytes. Many Holocene tufas are found along the Zrmanja River, Dalmatian karst, Croatia. In this work we present radiocarbon dating results of older tufa that was found for the first time at the Zrmanja River near the Village of Sanaderi. Tufa outcrops were observed at different levels, between the river bed and up to 26 m above its present level. Radiocarbon dating of the carbonate fraction revealed ages from modern, at the river bed, up to 40 kBP ~20 m above its present level. These ages fit well with the hypothesis that the Zrmanja River had a previous surface connection with the Krka River, and changed its flow direction toward the Novigrad Sea approximately 40 kBP (Marine Isotope Stage 3). Radiocarbon AMS dating of tufa organic residue yielded a maximum conventional age of 17 kBP for the highest outcrop position indicating probable penetration of younger organic material to hollow tufa structures, as confirmed by radiocarbon analyses of humin extracted from the samples. Stable carbon isotope composition (δ13C) of the carbonate fraction of (−10.4 ± 0.6)‰ and (−9.7 ± 0.8)‰ for the Holocene and the older samples, respectively, indicate the autochthonous origin of the carbonate. The δ13C values of (−30.5 ± 0.3)‰ and (−29.6 ± 0.6)‰ for organic residue, having ages <500 BP and >5000 BP, respectively, suggest a unique carbon source for photosynthesis, mainly atmospheric CO2, with an indication of the Suess effect in δ13C during last centuries. The oxygen isotopic composition (δ18O) agrees well with deposition of tufa samples in two stages, the Holocene (−8.02 ± 0.72‰) and “old” (mainly MIS 3 and the beginning of MIS 2) (−6.89 ± 0.34‰), suggesting a ~4 °C lower temperature in MIS 3 compared to the current one.

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The application of tritium, 2H, and 18O in the characterization of the precipitation, groundwater, and surface and lake water of the Plitvice Lakes (PL), Croatia, over the 1979–2019 period is presented. An increase in the mean annual air temperature of 0.06 °C/year and in the annual precipitation amount of 10 mm/year is observed. The good correlation of the tritium activity concentration in the PL and Zagreb precipitation implies that the tritium data for Zagreb are applicable for the study of the PL area. The best local meteoric water line at PL was obtained by the reduced major axis regression (RMA) and precipitation-weighted ordinary least squares regression (PWLSR) approaches: δ2HPWLSR = (7.97 ± 0.12) δ18O + (13.8 ± 1.3). The higher deuterium excess at PL (14.0 ± 2.2 ‰) than that at Zagreb reflects the higher altitude and influence of the Mediterranean precipitation. The δ2H in precipitation ranges from −132.4‰ to −22.3‰ and δ18O from −18.3 ‰ to −4.1‰. The much narrower ranges in the groundwater (<1‰ in δ18O, <10‰ in δ2H) indicate the good mixing of waters in aquifers and short mean residence times. The higher average δ2H in all three karst springs observed after 2003 can be attributed to the increase in the mean air temperature. The mean δ2H and δ18O values in the surface and lake water increase downstream due to the evaporation of surface waters. There is no significant difference between the surface water line and the lake water line (2011–2014). The stable isotope composition of the surface and lake waters reacts to extreme hydrological conditions.