Quantitative knowledge about the burial of sedimentary components at the seafloor has wide‐ranging implications in ocean science, from global climate to continental weathering. The use of ²³⁰Th‐normalized fluxes reduces uncertainties that many prior studies faced by accounting for the effects of sediment redistribution by bottom currents and minimizing the impact of age model uncertainty. Here we employ a recently compiled global data set of ²³⁰Th‐normalized fluxes with an updated database of seafloor surface sediment composition to derive atlases of the deep‐sea burial flux of calcium carbonate, biogenic opal, total organic carbon (TOC), nonbiogenic material, iron, mercury, and excess barium (Ba_xs). The spatial patterns of major component burial are mainly consistent with prior work, but the new quantitative estimates allow evaluations of deep‐sea budgets. Our integrated deep‐sea burial fluxes are 136 Tg C/yr CaCO₃, 153 Tg Si/yr opal, 20Tg C/yr TOC, 220 Mg Hg/yr, and 2.6 Tg Ba_xs/yr. This opal flux is roughly a factor of 2 increase over previous estimates, with important implications for the global Si cycle. Sedimentary Fe fluxes reflect a mixture of sources including lithogenic material, hydrothermal inputs and authigenic phases. The fluxes of some commonly used paleo‐productivity proxies (TOC, biogenic opal, and Ba_xs) are not well‐correlated geographically with satellite‐based productivity estimates. Our new compilation of sedimentary fluxes provides detailed regional and global information, which will help refine the understanding of sediment preservation.

Over the recent few decades, due to climate warming and the continuing exploration of Arctic seas’ mineral resources, the scientific interest in contamination problems has deepened significantly. In this study, for the first time, we characterize the distribution features of 47 elements (major and trace elements, including heavy metals, metalloid As, and Cs-137 technogenic radionuclide) in surface bottom sediments from some areas of the Barents, Kara, Laptev, and East-Siberian Seas. The lithogenic material was the main factor that controlled variability in many elements (Be, Al, Ti, Cr, Ga, Rb, Sr, Y, Zr, Nb, Ba, REE, Pb, Th, U, W, and Cs). Among the hydrogenic processes, the formation of Fe and Mn oxyhydroxides has the greatest impact on the Mn, Fe, Co, Ni, Cu, Ge, and Mo, and insignificantly V and Sb, variability in sediments. These, along with minor to moderate values of enrichment factor (EF) for most elements, allowed us to conclude that the observed element distribution is related to predominantly natural processes of thermal abrasion, river-run, and atmospheric input. The exception is As, which exhibited the elevated EF (up to 20) in the western and central Kara Sea, as well as in the Vilkitsky Strait. Since no significant relationship between As and Fe andMn oxyhydroxides distribution was found, we may assume primarily an anthropogenic source of As, related to the peat and/or coal combustion. According to the criteria of Ecological Risks assessment, all the examined areas have a low degree of risk. Data on the specific activity of Cs-137 correspond to the background average values characteristic for these regions. The highest levels of Cs-137 concentration (Bq/kg) were detected in the sediments of the Ob and Yenisei Rivers’ estuaries.

For the first time based on determination of the geochemical occurrence forms of trace metals the main processes that control the accumulation of elements (Al, Mn, Fe, Mo, Cr, Ni, Co, Cu, Pb, Cd, and As) in the recent sediment cores from the White Sea and Barents Sea were quantified. A high-resolution study of the bottom sediment cores allowed us to estimate the short-term variations (periodicity of 10–15 years) in the accumulation of metals to reveal the periods of maximum Fe and Mn contents in the amorphous hydroxides fraction, which serve as effective adsorbents of the trace elements majority, including heavy metals. The Mn/Fe ratio in the amorphous hydroxides phase can be considered as geochemical indicators of early diagenesis.

A comprehensive examination of the elemental (including radionuclides and heavy metals), mineral, and grain-size composition of sediments from different areas of the Barents Sea was performed. Sediment cores were sampled in the Central Deep, Cambridge Strait (Franz Josef Land Archipelago), Russkaya Gavan’ Bay (Novaya Zemlya Archipelago), and Bear Island Trough. We aim to evaluate how the modern and more ancient environmental conditions are reflected in the elemental and mineral composition, as well as to test indicative elemental ratios. The applied methods include elemental analysis using gamma-ray spectroscopy, X-ray fluorescence (XRF), Inductively Coupled Plasma-Mass Spectrometry (ICP-MS), and X-Ray Difractometry XRD analysis of minerals. Difference in sedimentation rates, grain-size composition, and sources of material, are reflected in downcore variation of Si/Al, Mn/Fe, P/Al, Ti/K, and quartz-feldspar ratios. At boundary Early Holocene/Late Deglaciation, intensive bottom currents from the West-Southern shelf areas contributed to increase of Si/Al and Zr/Ca ratios. Distinct growth of the Si/Fe ratio within the sediments deposited over Late Pleistocene to Mid Holocene may be caused by increased contents of the coarse sand material, as well as by abundant fluxes of clay-mineral-loaded glacial meltwater during the main deglaciation phase. The Mn/Fe ratio used as redox proxy, displayed peaks at different depths related to oxygen concentration growth in bottom water.

The Piip Volcano is a submarine volcanic edifice occupying the central part of the Volcanologists Massif in the southwestern Bering Sea, with two tops, southern and northern. The minimum depth of the northern top is located at 368 m, and of the southern at 464 m. Active hydrothermal venting occurring at both summits of the volcano supports diverse biological communities, including animals specific for chemosynthetic habitats. In benthic organisms inhabiting the northern and southern tops of the Piip Volcano, for the first time, we examined distribution patterns of the following trace elements: titanium, vanadium, chromium, manganese, iron, nickel, copper, zinc, arsenic, selenium, zirconium, molybdenum, silver, cadmium, antimony, barium, tungsten, lead, bismuth, and uranium. The element contents were quantified by the ICP-MS. Total carbon (TC) and total inorganic carbon (TIC) were determined using a Shimadzu TOC-L-CPN and mineral composition of sediment was determined using the XRD. In the water of the biotope from the northern top, concentrations of Mn, Zn, Ag, Cd, Sb, W, Pb were 2–6 times, and Ba was 50 times higher than those from the southern top. This was attributed to the lower temperature of fluids emanating at the southern top. An abundant population of Calyptogena pacifica (Bivalvia: Vesicomyidae: Pliocardiinae) was found only at the southern top. The main target of most trace elements, such as Fe, V, Cr, Co, Ni, Zn, As, Mo, Ag, Cd, W, Pb, Bi, and U were the soft parts of Calyptogena pacifica (with high TOC content, on average 53.1% in gills and 49.6% in the rest of the body). Gills were characterized by particular high contents (>100 µg g⁻¹ dry w.) of Zn, Cd, Fe, Ni, Cu, and Pb, which can form sulphides or be associated with them. Shells of C. pacifica, as well as Brachiopoda, were depleted in these elements, as well as tissues of the carnivores Paguridae (Crustacea) and Actiniaria (Anthozoa). In suspension feeders from both tops, the lower contents of most elements were detected. Estimation of Biological Concentration Factor (BCF) for most elements varied from 10² to 10⁴, reaching n10⁵ for Ni, Zn, Ag, Cd, and Pb. A significant difference in BCF values between Fe and Mn was revealed.