The Spatiotemporal Variability of Snowpack and Snowmelt Water <sup>18</sup>O and <sup>2</sup>H Isotopes in a Subarctic Catchment
Kashif Noor, Hannu Marttila, Bjørn Kløve, J. M. Welker, Pertti Ala‐aho
Abstract
Abstract This study provides a detailed characterization of spatiotemporal variations of stable water 18 O and 2 H isotopes in both snowpack and meltwater in a subarctic catchment. We performed extensive sampling and analysis of snowpack and meltwater isotopic compositions at 11 locations in 2019 and 2020 across three different landscape features: (a) forest hillslope, (b) mixed forest, and (c) open mires. The vertical isotope profiles in the snowpack's layered stratigraphy presented a consistent pattern in all locations before snowmelt, and isotope profiles homogenized during the peak melt period; represented by a 1–2‰ higher 18 O value than prior to melting. Our data indicated that the liquid‐ice fractionation was the prime reason that caused the depletion of heavy isotopes in initial meltwater samples prior to the peak melt period. The liquid‐ice fractionation was influenced by snowmelt rate, with higher fractionation during slow melt. The kinetic liquid‐ice fractionation was evident only in close examination of meltwater lc‐excess values, not 18 O values alone. Meltwater was isotopically heavier and more variable than the depth‐integrated snowpack; the weighted mean of meltwater isotope values was higher by 0.62–1.33‰ 18 O than the weighted mean of snowpack isotope values in forest hillslope and mixed forest areas, and 1.51–6.37‰ 18 O in open mires. Our results reveal close to 3.1‰ 18 O disparity between the meltwater and depth‐integrated snowpack isotope values prior to the peak melt period, suggesting that proper characterization of meltwater 18 O and 2 H values is vital for tracer‐based ecohydrological studies and models.