Ny-& Aring;lesund, located in Arctic Svalbard, is one of the most sensitive areas on Earth to global warming. In recent years, accelerated glacier ablation has become remarkable in Ny-& Aring;lesund. Glacial meltwaters discharge a substantial quantity of materials to the ocean, affecting downstream ecosystems and adjacent oceans. In August 2015, various water samples were taken near Ny-& Aring;lesund, including ice marginal meltwater, proglacial meltwater, supraglacial meltwater, englacial meltwater, and groundwater. Trace metals (Al, Cr, Mn, Fe, Co, Cu, Zn, Cd, and Pb), major ions, alkalinity, pH, dissolved oxygen, water temperature and electric conductivity were also measured. Major ions were mainly controlled by chemical weathering intensity and reaction types, while trace metals were influenced by both chemical weathering and physicochemical control upon their mobility. Indeed, we found that Br & oslash;ggerbreen was dominated by carbonate weathering via carbonation of carbonate, while Austre Lov & eacute;nbreen and Pedersenbreen were dominated by sulfide oxidation coupled with carbonate dissolution with a doubled silicate weathering. The higher enrichment of trace metals in supraglacial meltwater compared to ice marginal and proglacial meltwater suggested anthropogenic pollution from atmospheric deposition. In ice marginal and proglacial meltwater, principal component analysis indicated that trace metals like Cr, Al, Co, Mn and Cd were correlated to chemical weathering. This implies that under accelerated glacier retreat, glacier-derived chemical components are subjected to future changes in weathering types and intensity.

Glaciochemical records serve as one of the best archives and as good proxies to indicate regional and global anthropogenic influences. The Himalayas, with fragile ecosystems and pristine environments, hold the third largest reservoir of glacier ice and represent an ideal region to investigate trace metal pollution using glacier records. Limited studies on glacially recorded trace metals in the Himalayas usually collect samples from individual glaciers and report a few trace metals in different seasons. We provide a comprehensive and in-depth understanding of the glacially recorded trace metals in the central Himalayas regarding their spatial distribution, seasonal variability, and anthropogenic signals. We analyzed six representative metals (Cu, Zn, Cd, Cr, Pb, Co) and found that the trace metal concentration range largely varied between the studied metals and sampling sites. The Zn metal concentration is higher, attributed to the contribution of natural sources (e.g., forest fires, dust storms) and anthropogenic sources, including industrial and traffic-related emissions. The Pb concentration showed striking seasonality due to the relatively natural input of local material during the monsoon season and the regional and long-range transport of anthropogenic sources during the non-monsoon season. There was a clear spatial variation in certain trace metals, such as Cu, Zn, and Pb, showing decreasing trends with increasing elevation. The enrichment factor (EF) results showed that Zn metal was highly enriched, followed by Cu and Cd, indicating that Zn metal was relatively highly susceptible to intensified human activities. The seasonal paradox between the enrichment factor and metal concentration revealed that the EF of the monsoon season was usually higher than that of the non-monsoon season, and vice versa regarding metal concentrations primarily associated with metal deposition in regional climate regimes, particularly atmospheric circulation. We suggest that the analytical method can influence the trace metal concentration and EF calculation, resulting in a previously unrecognized bias in the seasonality of trace metals. Future research should prioritize stable isotopes of trace elements (e.g., Pb, Cu) in glaciers that would provide valuable information in identifying the potential source of anthropogenic inputs and the degree of extent affecting the glaciochemistry of the Himalayas.