Vertical profile of artificial radionuclide concentrations in the Central Arctic Ocean

The artificial radionuclides ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu and ²⁴¹Am have been measured in eight water samples collected in 1979, at intervals from surface to bottom, through the ice at the LOREX satellite camp SS near the North Pole. Differences in the concentrations and ratios of these nuclides, compared with values measured, over time, in the various water masses that flow into the Arctic Ocean, can be used as semi-independent checks on rates of flow to the LOREX stations and on residence times in the Arctic Ocean. An unexpected finding was that water labelled with low-level liquid waste from the Windscale plant on the Irish Sea is a major component of the 1500 m LOREX sample, and has reached there in no more than eight to ten years. Even from this one station in the Polar Ocean, estimation of the inventories of the various radionuclides is good enough to emphasize the importance of horizontal advection of the various supply terms to the Arctic.     

The dissolved Beryllium isotope composition of the Arctic Ocean

We present the first comprehensive set of dissolved ¹⁰Be and ⁹Be concentrations in surface waters and vertical profiles of all major sub-basins of the Arctic Ocean, which are complemented by data from the major Arctic rivers Mackenzie, Lena, Yenisey and Ob. The results show that ¹⁰Be and ⁹Be concentrations in waters below 150 m depth are low and only vary within a factor of 2 throughout the Arctic Basin (350-750 atoms/g and 9-15 pmol/kg, respectively). In marked contrast, Be isotope compositions in the upper 150 m are highly variable and show systematic variations. Cosmogenic ¹⁰Be concentrations range from 150 to 1000 atoms/g and concentrations of terrigenous ⁹Be range from 7 to 65 pmol/kg, resulting in ¹⁰Be/⁹Be ratios (atom/atom) between 0.5 and 14 × 10⁻⁸. Inflowing Atlantic water masses in the Eurasian Basin are characterized by a ¹⁰Be/⁹Be signature of 7 × 10⁻⁸. The inflow of Pacific water masses across the Bering Strait is characterized by lower ratios of 2-3 × 10⁻⁸, which can be traced into the central Arctic Ocean, possibly as far as the Fram Strait. A comparison of the high dissolved surface ¹⁰Be and ⁹Be concentrations (corresponding to low ¹⁰Be/⁹Be signatures of ∼2 × 10⁻⁸) in the Eurasian Basin with hydrographic parameters and river data documents efficient and rapid transport of Be with Siberian river waters across the Siberian Arctic shelves into the central Arctic Basin, although significant loss and exchange of Be on the shelves occurs. In contrast, fresh surface waters from the Canada Basin also show high cosmogenic ¹⁰Be contents, but are not enriched in terrigenous ⁹Be (resulting in high ¹⁰Be/⁹Be signatures of up to 14 × 10⁻⁸). This is explained by a combination of efficient scavenging of Be in the Mackenzie River estuary and the shelves and additional supply of cosmogenic ¹⁰Be via atmospheric fallout and melting of old sea ice. The residence time of Be in the deep Arctic Ocean estimated from our data is 800 years and thus similar to the average Be residence time in the global ocean.     

Cryosphere as a temporal sink and source of microplastics in the Arctic region

Microplastics (MPs) pollution has become a serious environmental issue of growing global concern due to the increasing plastic production and usage. Under climate warming, the cryosphere, defined as the part of Earth’s layer characterized by the low temperatures and the presence of frozen water, has been experiencing significant changes. The Arctic cryosphere (e.g., sea ice, snow cover, Greenland ice sheet, permafrost) can store and release pollutants into environments, making Arctic an important temporal sink and source of MPs. Here, we summarized the distributions of MPs in Arctic snow, sea ice, seawater, rivers, and sediments, to illustrate their potential sources, transport pathways, storage and release, and possible effects in this sentinel region. Items concentrations of MPs in snow and ice varied about 1–6 orders of magnitude in different regions, which were mostly attributed to the different sampling and measurement methods, and potential sources of MPs. MPs concentrations from Arctic seawater, river/lake water, and sediments also fluctuated largely, ranging from several items of per unit to >40,000 items m^?3, 100 items m^?3, and 10,000 items kg^?1 dw, respectively. Arctic land snow cover can be a temporal storage of MPs, with MPs deposition flux of about (4.9–14.26) × 10⁸ items km^?2 yr^?1. MPs transported by rivers to Arctic ocean was estimated to be approximately 8–48 ton/yr, with discharge flux of MPs at about (1.65–9.35) × 10⁸ items/s. Average storage of MPs in sea ice was estimated to be about 6.1×10¹⁸ items, with annual release of about 5.1×10¹⁸ items. Atmospheric transport of MPs from long-distance terrestrial sources contributed significantly to MPs deposition in Arctic land snow cover, sea ice and oceanic surface waters. Arctic Great Rivers can flow MPs into the Arctic Ocean. Sea ice can temporally store, transport and then release MPs in the surrounded environment. Ocean currents from the Atlantic brought high concentrations of MPs into the Arctic. However, there existed large uncertainties of estimation on the storage and release of MPs in Arctic cryosphere owing to the hypothesis of average MPs concentrations. Meanwhile, representatives of MPs data across the large Arctic region should be mutually verified with in situ observations and modeling. Therefore, we suggested that systematic monitoring MPs in the Arctic cryosphere, potential threats on Arctic ecosystems, and the carbon cycle under increasing Arctic warming, are urgently needed to be studied in future.     

Modern river discharge and pathways of supplied material in the Eurasian Arctic Ocean: evidence from mineral assemblages and major and minor element distribution

Clay-mineral, heavy-mineral, and elemental distributions in sediments from the Arctic Ocean and the adjacent Laptev and Kara seas can be attributed to the geology of the hinterland and the transport of terrigenous material by rivers onto the shelves. Kara Sea sediments are characterized by increased contents of smectite and elevated Ni/Al-, Ti/Al-, and Cr/Al ratios. In the western Laptev Sea sediments are enriched in smectite and clinopyroxene and increased in Ti/Al-, Cr/Al-, and Ca/Al ratios. The composition of the sediments reflects suspended matter input from the large trap basalt of the Putoran Mountains. The eastern Laptev Sea sediments display increased illite and amphibole contents as well as a chemical composition similar to average shale. This composition is due to the discharge from the Lena and Yana rivers, which drain a large catchment area consisting of sedimentary Mesozoic and Paleozoic rocks. Material from the eastern Laptev Sea is transported by ocean currents and sediment-laden sea ice along the Transpolar Drift into the central Arctic Ocean. This is indicated by similar values of Ti/Al-, Cr/Al-, Rb/Al-, and K/Al ratios as well as increased concentrations of amphibole and illite, determined in sediments from the Lomonosov Ridge. A minor input from the Beaufort Sea into the central Arctic Ocean is suggested from increased Ca/Al ratios and increased contents of opaque minerals.     

Seasonal and Annual Fluxes of Nutrients and Organic Matter from Large Rivers to the Arctic Ocean and Surrounding Seas

River inputs of nutrients and organic matter impact the biogeochemistry of arctic estuaries and the Arctic Ocean as a whole, yet there is considerable uncertainty about the magnitude of fluvial fluxes at the pan-Arctic scale. Samples from the six largest arctic rivers, with a combined watershed area of 11.3?×?10⁶?km², have revealed strong seasonal variations in constituent concentrations and fluxes within rivers as well as large differences among the rivers. Specifically, we investigate fluxes of dissolved organic carbon, dissolved organic nitrogen, total dissolved phosphorus, dissolved inorganic nitrogen, nitrate, and silica. This is the first time that seasonal and annual constituent fluxes have been determined using consistent sampling and analytical methods at the pan-Arctic scale and consequently provide the best available estimates for constituent flux from land to the Arctic Ocean and surrounding seas. Given the large inputs of river water to the relatively small Arctic Ocean and the dramatic impacts that climate change is having in the Arctic, it is particularly urgent that we establish the contemporary river fluxes so that we will be able to detect future changes and evaluate the impact of the changes on the biogeochemistry of the receiving coastal and ocean systems.     

Hafnium isotopes in Arctic Ocean water

The first isotopic compositions of dissolved hafnium in seawater from across the Arctic Ocean are reported. Most samples from the four sub-basins of the Arctic Ocean have values within error of an average of ε_Hf = +0.8. Combined Hf-Nd isotope compositions do not fall on the well-established positive correlation for mantle and crustal rocks. Instead, Arctic waters have Hf that is more radiogenic than that typically found in rocks with similar Nd isotope compositions, a feature previously found in ferromanganese crusts and waters from the Pacific Ocean. Arctic seawater samples generally fall on the lower part of the ferromanganese crust array, reflecting influences of inputs from Arctic rivers and interactions of shelf waters with underlying sediments. Arctic rivers have much higher Hf concentrations (7-30 pM) than Arctic seawater (0.36-4.2 pM). Water from the Mackenzie River has the least radiogenic Hf, with ε_Hf = −7.1 ± 1.7, and plots furthest away from the ferromanganese crust array, while waters from the Ob, Yenisey, and Lena Rivers have values that are indistinguishable from most Arctic waters. In the Amundsen, Makarov, and Canada basins, Hf concentrations are highest at the surface and lowest in the deeper waters, reflecting the influences of riverine inputs and of waters that have flowed over the extensive Siberian continental shelves and have Nd and Hf characteristics that reflect water-sediment interactions. This is in contrast to the relatively low near surface Hf concentrations reported for locations elsewhere. The Pacific water layer in the Canada Basin exhibits the highest value of ε_Hf = +6.8 ± 1.8, reflecting the Hf isotopic composition of waters entering the Arctic from the Pacific Ocean. Mixing relationships indicate that a substantial fraction of the Hf in the Mackenzie River is lost during estuarine mixing; the behaviour of Hf from other rivers is less constrained.     

Dissolved Al, In, and Ce in the eastern Indian Ocean and the Southeast Asian Seas in comparison with the radionuclides Pb and Po

To carry out comparative geochemical investigation of refractory and reactive metals in different oceanic settings covering different θ-S characteristics, productivity, dissolved oxygen profiles, water and sediment discharge, etc., we have determined the vertical profiles of dissolved (<0.04 μm) Al, In and Ce, as well as ²¹⁰Pb and ²¹⁰Po in the eastern Indian Ocean (from 40°S in the Southern Ocean to 8°N in the Bay of Bengal) and the Southeast Asian Seas. In the Antarctic Circumpolar Region, the concentrations of these refractory metals are very low, presumably due to very low the atmospheric input and intensified scavenging. Resemblance in the vertical profiles of these metals is often seen in some other stations. However, there are also significant differences among their distributions, for example, in the magnitude of surface enrichment caused by the external input from eolian and fluvial-coastal sources. Comparison of Al distributions in surface waters with those of atmospherically derived ²¹⁰Pb suggests the relative importance of eolian input over fluvial-coastal sources. Fluvial and coastal input appears to be insignificant for dissolved In, but may be important for Ce. The mean residence time of Al in the surface mixed layer was estimated to be ∼2 years which is similar to that of ²¹⁰Pb.In the intermediate and deep waters, the concentrations of each element vary with depth and location. The range of variation is in the order of Al>Ce>In, depending upon particle reactivity. Although dissolved Al decreases along the water trajectory by particle scavenging, variations of dissolved In and Ce are relatively small which may be due to less scavenging for both elements. Compared with significantly high (>4 pM) dissolved Ce throughout the water column in the Bay of Bengal, dissolved Al concentration remains low, suggesting that it has higher affinity to particles and hence is scavenged by sinking particulate matter. This is consistent with the observation that the dissolved Al in the Antarctic Intermediate Water (AAIW) decreases from 4 to 6 nM in the 30°S Perth Basin to <0.7 nM in the 10°S West Australia Basin along its trajectory. Using the chlorofluorocarbons (CFCs) ventilation age of AAIW (Fine, 1993), the mean residence time of Al in the intermediate and deep waters in the eastern Indian Ocean is estimated to be <17 yr, approximately the same as that of ²¹⁰Pb (10-15 yr). In the semiclosed basins of Southeast Asia, the distributions of Al, In and Ce are also very unique. In the South China Sea, there is a strong sediment source for dissolved In and Ce during the deepwater passage through the Luzon Strait.     

Manganese Sources and Sinks in the Arctic Ocean with Reference to Periodic Enrichments in Basin Sediments

Between 1990 and 2007, twenty-nine box cores were recovered within the Arctic Ocean spanning shelf, slope and basin locations, and analyzed for aluminum (Al), manganese (Mn), other inorganic components and organic carbon (C_Org). Using these core data together with literature values, we have constructed budgets for Al and Mn in the Arctic Ocean. Most of the Al and Mn entering the Arctic comes from rivers or coastal erosion, and almost all of these two elements is trapped within the Arctic. Total Mn distributions in sediments reflect the recycling and loss of much of the Mn from shelf sediments with ultimate burial over the slopes and in basins. Mn enrichments observed as bands in long cores from the basins appear to co-occur with inter-glacial periods. Our Mn budget suggests that change in sea level associated with the accumulation and melting of glaciers is a likely cause for the banding. The Arctic Ocean, which presently contains as much as 50% shelf area, loses most of that when global sea level falls by?~120?m during glacial maxima. With lower sea level, Mn input from rivers and coastal erosion declines, and inputs become stored in permafrost on the sub-aerial shelves or at the shelf margin. Sea-level rise re-establishes coastal erosion and large riverine inputs at the margin and initiates the remobilization of Mn stored on shelves by turning on algal productivity, which provides the C_Org required to reduce sedimentary Mn oxyhydroxides.     

Marine biogeochemistries of Be and Al: A study based on cosmogenic10Be, Be and Al in marine calcite, aragonite, and opal

The geochemical behaviors of Be and Al in ocean waters have been successfully studied in recent years using natural, cosmogenic, radioactive¹⁰Be and²⁶Al as tracers. The present day dissolved concentrations and distribution of the stable and radioactive isotopes of Be and Al in ocean waters have revealed their short residence times and appreciable effects of exchange fluxes at the coastal and ocean-sediment interfaces. It follows that concentrations of these particle-active elements must have varied in the past with temporal changes in climate, biological productivity and aeolian flux of continental detritus to the oceans. We therefore investigated the feasibility of extending the measurements of Be and Al isotope concentrations in marine systems to the 10³–10⁶ y BP time scale. We report here the discovery of significant amounts of intrinsic Be and Al in marine foraminiferal calcite and coral aragonite, and of Al in opal (radiolarians) and aragonite (coral), which makes it possible to determine¹⁰Be/Be and²⁶Al/Al in oceans in the past. We also report measured¹⁰Be/⁹Be in foraminiferal calcite in Pacific Ocean cores, which reveal that the concentrations and ratios of the stable and cosmogenic isotopes of Be and Al have varied significantly in the past 30 ky. The implications of these results are discussed.     

Manganese-rich brown layers in Arctic Ocean sediments: Composition, formation mechanisms, and diagenetic overprint

We present inorganic geochemical analyses of pore waters and sediments of two Late Quaternary sediment cores from the western Arctic Ocean (southern Mendeleev Ridge, RV Polarstern Expedition ARK-XXIII/3), focussing on the composition and origin of distinct, brown-colored, Mn-rich sediment layers. Carbonate enrichments occur in association with these layers as peaks in Ca/Al, Mg/Al, Sr/Al and Sr/Mg, suggesting enhanced input of both ice-rafted and biogenic carbonate. For the first time, we show that the Mn-rich layers layers are also consistently enriched in the scavenged trace metals Co, Cu, Mo and Ni. Distinct bioturbation patterns, specifically well-defined brown burrows into the underlying sediments, suggest these metal enrichments formed close to the sediment-water interface. The geochemical signature of these metal- and carbonate-rich layers most probably documents formation under warmer climate conditions with an intensified continental hydrological cycle and only seasonal sea ice cover. Both rivers and sea ice delivered trace metals to the Arctic Ocean, while enhanced seasonal productivity exported reactive organic matter to the sea floor. The coeval deposition of organic matter, Mn (oxyhydr)oxides and trace metals triggered intense diagenetic Mn cycling at the sediment-water interface. These processes resulted in the formation of Mn and trace metal enrichments, and the degradation of labile organic matter. With the onset of cooler conditions, reduced riverine runoff and/or a solid sea ice cover terminated the input of riverine trace metal and fresh organic matter, resulting in deposition of grayish-yellowish, metal-poor sediments. Oxygen depletion of Arctic bottom waters under these cooler conditions is not supported by our data, and did not cause the sedimentary Mn distribution. While the original composition and texture of the brown layers resulted from specific climatic conditions and corresponding diagenetic processes, pore water data show that diagenetic Mn redistribution is still affecting the organic-poor deeper sediments. Given persistent steady state conditions, purely authigenic Mn-rich brown layers may form, while others may be partly or completely dissolved. The degree of diagenetic Mn redistribution largely depends on the depositional environment, the Mn and organic matter availability, and apparently affected the Co/Mo ratios of Mn-rich layers. Thus, brown Arctic layers are not necessarily synchronous features, and should not be correlated across the Arctic Ocean without additional age control.     

Glacial Lake Vitim, a 3000-km outburst flood from Siberia to the Arctic Ocean

A prominent lake formed when glaciers descending from the Kodar Range blocked the River Vitim in central Transbaikalia, Siberia. Glacial Lake Vitim, evidenced by palaeoshorelines and deltas, covered 23,500 km² and held a volume of ~ 3000 km³. We infer that a large canyon in the area of the postulated ice dam served as a spillway during an outburst flood that drained through the rivers Vitim and Lena into the Arctic Ocean. The inferred outburst flood, of a magnitude comparable to the largest known floods on Earth, possibly explains a freshwater spike at ~ 13 cal ka BP inferred from Arctic Ocean sediments.     

Surmounting luminescence age overestimation in Alaska-margin Arctic Ocean sediments by use of ‘micro-hole’ quartz dating

Because of several difficulties with the application of radiocarbon (¹⁴C) dating to Arctic Ocean sediments, numeric dating techniques are needed that can complement, supplant and reach beyond the ¹⁴C method. However, large age overestimates (often >7 kyr) for near-sediment-water-interface horizons from Arctic Ocean cores have been almost universal when luminescence dating has been applied to multigrain aliquots of fine silt (4–11 μm) quartz and feldspar grains. Here micro-hole quartz-grain photon-stimulated-luminescence (PSL) dating is applied to the 0.5–2.0 cm horizons of multicores from high-sedimentation-rate sites spanning depths from 87 m to 1140 m at the Alaska margin of the Arctic Ocean. Expected near zero ages (0–200 a) result when grains larger than ～11 μm are used, demonstrating that fine-silt age overestimations here and perhaps elsewhere in the Arctic Ocean are a function of grain and aliquot size. At the 87 m site, the micro-hole PSL approach revealed no significant gradient in age estimates over the 1–26 cm horizon range, implying that bioturbation reached to at least 26 cm. Micro-hole PSL dating of 25–62 μm quartz grains from trans-ocean sea-ice sediment also produced expected near zero ages, in contrast to earlier reported long-bleach multigrain PSL results from 4–11 μm fractions of the same samples. The micro-hole PSL approach thus surmounts the age overestimation problem associated with the use of multigrain silt fractions, and overcomes limitations of the ¹⁴C method in this region. Finally, results unexpectedly suggest the potential of micro-hole quartz PSL for use in provenance studies of Arctic Ocean sea-ice sediment.     

极地海洋钻探研究进展

南极和北极海域的深海钻探（DSDP）和大洋钻探（ODP）研究所取得的成就是举世瞩目的,为人类研究过去全球变化打开了新的视野。它们揭示了北大西洋高纬度海区新近纪的古海洋学和古气候的演化历史,发现了早更新世"41ka世界"千年尺度的气候波动,以及冰期表层水温与深层水的耦合颤动,说明冰期旋回中冰消期气候的不稳定性。检验了新近纪环南极洋流的形成历史,并揭示了南极新生代的气候变冷和冰盖的演变历史,以及证实了南大洋温度变化领先于全球冰量的变化。2004年北极罗蒙诺索脊的综合大洋钻探（IODP）将宣告科学探索时代的到来,其研究将重建北冰洋新生代环境变化和气候的演变历史,展示北冰洋在全球气候变化中的作用。     

Alkane and PAH biomarkers as tracers of terrigenous organic carbon in Arctic Ocean sediments

We present the first sedimentary biomarker study encompassing the entire Arctic Ocean. A large data set of organic markers for terrigenous, petroleum and combustion inputs [alkanes, hopanes and steranes, parent and alkyl polycyclic aromatic hydrocarbons (PAHs)] is examined for patterns in space and time using principal components analysis (PCA) and partial least squares (PLS). Biomarker patterns reveal the central Arctic Ocean basin sediments to be compositionally distinct from those of the Mackenzie River/Beaufort Sea and Barents Sea, but similar to those of the Laptev Sea. PAH distributions reflected in PAH ratios and PCA projections demonstrate that Arctic Ocean sediment is dominated by natural inputs to the extent that anthropogenic combustion PAHs are not significant. We find only modest changes between the glacial and post-glacial sediments for atmospherically transported hydrocarbon biomarkers, while particle associated biomarkers were captured strongly at basin edges during the glacial period, and much more evenly transported across basins during the post-glacial period. The orders of magnitude decreases in particle associated petrogenic alkanes and PAHs in central basins during glacial times, coupled with the uniformity of most petrogenic biomarker parameters for most basin and shelf locations, reflect a massive reduction in ice transport that makes the margins the most likely source of petrogenic material for the Pleistocene/Holocene central Arctic basins. The proximity of large coal deposits of various maturity levels along the Lena River, the overlap in PAH and biomarker composition of the Laptev Sea and surficial sediments from the central Arctic Ocean and the location of the Laptev Sea at the origin of the main Transpolar Drift all point to eroded coals from the Lena River/Laptev Sea as the likely source of petrogenic hydrocarbons to the central Arctic Ocean. The ubiquitous presence of allochthonous coal in Arctic Ocean surface sediments provides a major constraint on the use of petrogenic biomarkers to infer the presence of subsurface petroleum reserves.     

The distribution of neodymium isotopes in Arctic Ocean basins

Nd concentration and isotope data have been obtained for the Canada, Amundsen, and Makarov Basins of the Arctic Ocean. A pattern of high Nd concentrations (up to 58 pM) at shallow depths is seen throughout the Arctic, and is distinct from that generally seen in other oceans where surface waters are relatively depleted. A range of isotopic variations across the Arctic and within individual depth profiles reflects the different sources of waters. The dominant source of water, and so Nd, is the Atlantic Ocean, with lesser contributions from the Pacific and Arctic Rivers. Radiogenic isotope Nd signatures (up to ε_Nd = −6.5) can be traced in Pacific water flowing into the Canada Basin. Waters from rivers draining older terrains provide very unradiogenic Nd (down to ε_Nd = −14.2) that can be traced in surface waters across much of the Eurasian Basin. A distinct feature of the Arctic is the general influence of the shelves on the Nd concentrations of waters flowing into the basins, either from the Pacific across the Chukchi Sea, or from across the extensive Siberian shelves. Water-shelf interaction results in an increase in Nd concentration without significant changes in salinity in essentially all waters in the Arctic, through processes that are not yet well understood. In estuarine regions other processes modify the Nd signal of freshwater components supplied into the Arctic Basin, and possibly also contribute to sedimentary Nd that may be subsequently involved in sediment-water interactions. Mixing relationships indicate that in estuaries, Nd is removed from major river waters to different degrees. Deep waters in the Arctic are higher in Nd than the inflowing Atlantic waters, apparently through enrichments of waters on the shelves that are involved in ventilating the deep basins. These enrichments generally have not resulted in major shifts in the isotopic compositions of the deep waters in the Makarov Basin (ε_Nd ∼ −10.5), but have created distinctive Nd isotope signatures that were found near the margin of the Canada Basin (with ε_Nd ∼ −9.0). The deep waters of the Amundsen Basin are also distinct from the Atlantic waters (with ε_Nd = −12.3), indicating that there has been limited inflow from the adjacent Makarov Basin through the Lomonosov Ridge.     

An 11 000‐year record of driftwood delivery to the western Queen Elizabeth Islands,Arctic Canada

Fifty‐six new radiocarbon dates from driftwood (mainly Larix, Picea and Populus spp.) collected from the modern and raised shorelines of Melville and Eglinton islands (western Canadian High Arctic) are presented and compared to other driftwood collections from the Canadian Arctic Archipelago (CAA) and Greenland. By documenting the species (provenance) and spatio‐temporal distribution of driftwood at various sites across the Arctic, regional characterizations of former sea‐ice conditions and changes in Arctic Ocean circulation patterns may be deduced. The earliest postglacial invasion of the Canadian Arctic Archipelago by driftwood is recorded on central Melville Island at c. 11 cal. ka BP, suggesting that the modern circulation pattern of Arctic Ocean surface water southeast through the archipelago was established >1000 years earlier than previously proposed. Throughout most of the Holocene until c. 1.0 cal. ka BP, the rate of driftwood delivery to the western Arctic islands was low (~1 recorded stranding event per 200 years) and intermittent, with the longest break in the record occurring between c. 3.0 and 5.0 cal. ka BP. This 2000‐year hiatus is attributed to a period of colder temperatures causing severe sea‐ice conditions and effectively making the coasts of the western Arctic islands inaccessible. After c. 1.0 cal. ka BP, driftwood incursion increased to maximum Holocene levels (~1 recorded stranding event every 20 years). Driftwood identified to the genus level as Larix that was delivered at this time suggests that the Trans Polar Drift current was regularly in its most southwestern position, related to a dominantly positive Arctic Oscillation mode. The Little Ice Age appears to have had little impact on driftwood entry to the western Canadian Arctic Archipelago, indeed the general abundance in the latest Holocene may record infrequent landfast sea ice.     

New evidence from the western Canadian Arctic Archipelago for the resubmergence of Bering Strait

Widespread molluscan samples were collected from raised marine sediments to date the last retreat of the NW Laurentide Ice Sheet from the western Canadian Arctic Archipelago. At the head of Mercy Bay, northern Banks Island, deglacial mud at the modern coast contains Hiatella arctica and Portlandia arctica bivalves, as well as Cyrtodaria kurriana, previously unreported for this area. Multiple H. arctica and C. kurriana valves from this site yield a mean age of 11.5 ¹⁴C ka BP (with 740 yr marine reservoir correction). The occurrence of C. kurriana, a low Arctic taxon, raises questions concerning its origin, because evidence is currently lacking for a molluscan refugium in the Arctic Ocean during the last glacial maximum. Elsewhere, the oldest late glacial age available on C. kurriana comes from the Laptev Sea where it is < 10.3 ¹⁴C ka BP and attributed to a North Atlantic source. This is 2000 cal yr younger than the Mercy Bay samples reported here, making the Laptev Sea, ~ 3000 km to the west, an unlikely source. An alternate route from the North Atlantic into the Canadian Arctic Archipelago was precluded by coalescent Laurentide, Innuitian and Greenland ice east of Banks Island until ~ 10 ¹⁴C ka BP. We conclude that the presence of C. kurriana on northern Banks Island records migration from the North Pacific. This requires the resubmergence of Bering Strait by 11.5 ¹⁴C ka BP, extending previous age determinations on the reconnection of the Pacific and Arctic oceans by up to 1000 yr. This renewed ingress of Pacific water likely played an important role in re-establishing Arctic Ocean surface currents, including the evacuation of thick multi-year sea ice into the North Atlantic prior to the Younger Dryas geochron.     

New constraints on elemental and Pb and Nd isotope compositions of South American and Southern African aerosol sources to the South Atlantic Ocean

Improving the geochemical database available for characterising potential natural and anthropogenic aerosol sources from South America and Southern Africa is a critical precondition for studies aimed at understanding trace metal controls on the marine biogeochemical cycles of the South Atlantic Ocean. We here present new elemental and isotopic data for a wide range of sample types from South America and Southern Africa that are potentially important aerosol sources. This includes road dust from Buenos Aires and lichen samples from Johannesburg, soil dust from Patagonia, volcanic ash from the Andean volcanic belt, and aerosol samples from São Paulo. All samples were investigated for major (Al, Ca, Fe, Mg, Na, K, Mn) and trace element (Cd, Co, Cr, Cu, Ni, Pb, REE, Sc, Th, Y, V, Zn) concentrations and Nd and Pb isotopic compositions. We show that diagrams of ²⁰⁸Pb/²⁰⁷Pb vs. ε_Nd, ²⁰⁸Pb/²⁰⁷Pb vs. Pb/Al, 1/[Pb], Zn/Al, Cd/Al, Cu/Al, and ε_Nd vs. Pb/Al, and 1/[Nd] are best suited to separate South American and South African source regions as well as natural and anthropogenic sources. A subset of samples from Patagonia and the Andes was additionally subjected to separation of a fine (<5?μm) fraction and compared to the composition of the bulk sample. We show that differences in the geochemical signature of bulk samples between individual regions and source types are significantly larger than between grain sizes. Jointly, these findings present an important step forward towards a quantitative assessment of aeolian trace metal inputs to the South Atlantic Ocean.     

Clay-mineral distribution in surface sediments of the Eurasian Arctic Ocean and continental margin as indicator for source areas and transport pathways — a synthesis

Clay-mineral distributions in the Arctic Ocean and the adjacent Eurasian shelf areas are discussed to identify source areas and transport pathways of terrigenous material in the Arctic Ocean. The main clay minerals in Eurasian Arctic Ocean sediments are illite and chlorite. Smectite and kaolinite occur in minor amounts in these sediments, but show strong variations in the shelf areas. These two minerals are therefore reliable in reconstructions of source areas of sediments from the Eurasian Arctic. The Kara Sea and the western part of the Laptev Sea are enriched in smectite, with highest values of up to 70% in the deltas of the Ob and Yenisey rivers. Illite is the dominant clay mineral in all the investigated sediments except for parts of the Kara Sea. The highest concentrations with more than 70% illite occur in the East Siberian Sea and around Svalbard. Chlorite represents the clay mineral with lowest concentration changes in the Eastern Arctic, ranging between 10 and 25%. The main source areas for kaolinite in the Eurasian Arctic are Mesozoic sedimentary rocks on Franz-Josef Land islands. Based on clay-mineral data, transport of the clay fraction via sea ice is of minor importance for the modern sedimentary budget in the Arctic basins.     

The Arctic Coastal Dynamics Database: A New Classification Scheme and Statistics on Arctic Permafrost Coastlines

Arctic permafrost coasts are sensitive to changing climate. The lengthening open water season and the increasing open water area are likely to induce greater erosion and threaten community and industry infrastructure as well as dramatically change nutrient pathways in the near-shore zone. The shallow, mediterranean Arctic Ocean is likely to be strongly affected by changes in currently poorly observed arctic coastal dynamics. We present a geomorphological classification scheme for the arctic coast, with 101,447?km of coastline in 1,315 segments. The average rate of erosion for the arctic coast is 0.5?m? year^?1 with high local and regional variability. Highest rates are observed in the Laptev, East Siberian, and Beaufort Seas. Strong spatial variability in associated database bluff height, ground carbon and ice content, and coastline movement highlights the need to estimate the relative importance of shifting coastal fluxes to the Arctic Ocean at multiple spatial scales.