Deglaciation has accelerated the transport of minerals as well as modern and ancient organic matter from land to fjord sediments in Spitsbergen, Svalbard, in the European Arctic Ocean. Consequently, such sediments may contain significant levels of total mercury (THg) bound to terrestrial organic matter. The present study compared THg contents in surface sediments from three fjord settings in Spitsbergen: Hornsund in the southern Spitsbergen, which has high annual volume of loss glacier and receives sediment from multiple tidewater glaciers, Dicksonfjorden in the central Spitsbergen, which receives sediment from glacifluvial rivers, and Wijdefjorden in the northern Spitsbergen, which receive sediments from a mixture of tidewater glaciers and glacifluvial rivers. Our results showed that the THg (52 ± 15 ng g −1) bound to organic matter (OM) was the highest in the Hornsund surface sediments, where the glacier loss (0.44 km 3 yr −1) and organic carbon accumulation rates (9.3 ~ 49.4 g m −2 yr −1) were elevated compared to other fjords. Furthermore, the δ 13 C (-27 ~-24‰) and δ 34 S values (-10 ~ 15‰) of OM indicated that most of OM were originated from terrestrial sources. Thus, the temperature-driven glacial melting could release more oM originating from the meltwater or terrestrial materials, which are available for THg binding in the European Arctic fjord ecosystems. Increasing temporal trends of total mercury (THg) concentration in the sediments of the Arctic continental shelves and lakes have recently been reported 1,2. These increasing levels have been proposed to be caused by the long-distance transport of anthropogenic mercury (Hg) from industrialized countries to the Arctic, given its long atmospheric lifetime of 0.3 to 2 years 3,4. In addition, it has been shown that ' Atmospheric Mercury Depletion Events' (AMDE) in the spring can lead to high Hg deposition in the Arctic Ocean. Reactive Hg (Hg 2+) is rapidly formed through in situ oxidation of gaseous Hg° by halogens (i.e., atomic Br and radical BrO), which are generated by solar irradiation through O 3 destruction 5-7. However, previous measurements of atmospheric Hg deposition in the Arctic regions have revealed relatively low deposition rates of <5 µg m −2 yr −1 8. Recent studies have suggested that natural processes governing Hg release via riverine transport 9 , soil runoff, and/or discharge of water coming from thawing permafrost 10 could be important sources of Hg to the Arctic environments. Fjords on Svalbard, the main island of the Svalbard archipelago, is among the most studied fjord systems in the world 11. Previous studies have focused on the effects of local and/or long-range transport, oceanic currents, and long-term sediment deposition rates (i.e., geological and chemical processes that control Hg distribution in surface and core sediments) 4,12-17 on spatial distribution and the extent of accumulation of Hg in the fjord sediment. Recent studies have shown that fjords are effective sequesters of organic carbon among other marine