[1] Time series measurements of the nuclear fuel reprocessing tracers, 129 I and 137 Cs, and ventilation tracer, CFC-11, were used to determine circulation time scales for Atlantic Water (AW) in the Arctic Ocean. Measurements in surface water are consistent with an advection model and transit times from the North Sea of 1-4 years to the Barents Sea, 3-6 years to the Kara Sea, and 9-12 years to the North Pole.

[1] The loss of Arctic sea ice has accelerated in recent years. With the decline in sea ice cover, the Arctic Ocean biogeochemistry is undergoing unprecedented change. A key question about the changing Arctic Ocean biogeochemistry is concerning the impact of the shrinking sea ice cover on the particulate organic carbon (POC) export from the upper Arctic Ocean. Thus far, there are still very few direct measurements of POC export in the permanently ice-covered central Arctic Ocean. A further issue is that the magnitude of the POC export so far documented in this region remains controversial. During the ARK-XXII/2 expedition to the Arctic Ocean from 28 July to 7 October in 2007, we conducted a high-resolution study of POC export using 234 Th/ 238 U disequilibrium. Depth profiles of total 234 Th in the upper 200 m were collected at 36 stations in the central Arctic Ocean and its adjacent seas, i.e., the Barents Sea, the Kara Sea and the Laptev Sea. Samples were processed using a small-volume MnO 2 coprecipitation method with addition of a yield tracer, which resulted in one of the most precise 234 Th data sets ever collected. Thorium-234 deficit with respect to 238 U was found to be evident throughout the upper 100 m over the Arctic shelves. In comparison, 234 Th deficit was confined to the upper 25 m in the central Arctic Ocean. Below 25 m, secular equilibrium was approached between 234 Th and 238 U. The observed 234 Th deficit was generally associated with enhanced total chlorophyll concentrations, indicating that in situ production and export of biogenic particles are the main mechanism for 234 Th removal in the Arctic Ocean. Thorium-234-derived POC fluxes were determined with a steady state model and pump-normalized POC/ 234 Th ratios on total suspended particles collected at 100 m. Results showed enhanced POC export over the Arctic shelves. On average, POC export fluxes over the various Arctic shelves were 2.7 ± 1.7 mmol m −2 d −1 (the Barents Sea), 0.5 ± 0.8 mmol m −2 d −1 (the Kara Sea), and 2.9 ± 1.8 mmol m −2 d −1 (the Laptev Sea) respectively. In comparison, the central Arctic Ocean was characterized by the lowest POC export flux ever reported, 0.2 ± 1.0 mmol m −2 d −1 (1 standard deviation, n = 26). This value is very low compared to prior estimates and is also much lower than the POC export fluxes reported in other oligotrophic oceans. A ThE ratio ( 234 Th-derived POC export/primary production) of <6% in the central Arctic Ocean was estimated using the historical measurements of primary production. The low ThE ratio indicates that like other oligotrophic regimes, the central Arctic Ocean is characterized by low POC export relative to primary production, i.e., a tightly coupled food web. Our study strongly suggests that the current role of the central Arctic Ocean in C sequestration is still very limited. Meanwhile, this role might be altered because of global warming and future decline in sea ice cover.

1] Particulate organic carbon (POC) export fluxes were estimated in the shelf-slope region of the Chukchi Sea using measurements of 234 Th À238 U disequilibria and the POC/ 234 Th ratio in large (>53-mm) particles. These export fluxes were used in conjunction with rates of primary productivity and benthic carbon respiration to construct a POC budget for this shelf-slope region. Samples were collected along a series of shelf-basin transects in the spring (May-June) and summer (July-August) of 2004. These stations were previously occupied during the ice covered (spring) and open water (summer) seasons of 2002, allowing for an interannual comparison of export flux. In contrast to 2002, when open water POC fluxes were significantly higher than in the ice-covered period, POC export fluxes in 2004 were similar during the spring (average = 19.7 ± 24.8 mmol C m À2 d À1 ) and summer (average = 20.0 ± 14.5 mmol C m À2 d À1 ). The high POC fluxes measured during the spring are attributed to a plankton bloom, as evidenced by exceptionally high rates of primary productivity (average = 124.4 ± 88.1 mmol C m À2 d À1 ). The shelf-slope budget of particulate organic carbon indicates that 10-20% of primary productivity was exported below 50 m but was not consumed during benthic carbon respiration or burial and oxidation in underlying sediments. Furthermore, a water columnÀsediment budget of 234 Th indicates that particulate material is retained in shelf sediments on a seasonal basis.

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In this study we present dissolved and particulate 230 Th and 232 Th results, as well as particulate 234 Th data, obtained as part of the GEOTRACES central Arctic Ocean sections GN04 (2015) and IPY11 (2007).Samples were analyzed following GEOTRACES methods and compared to previous results from 1991. We observe significant decreases in 230 Th concentrations in the deep waters of the Nansen Basin. We ascribe this nonsteady state removal process to a variable release and scavenging of trace metals near an ultraslow spreading ridge. This finding demonstrates that hydrothermal scavenging in the deep-sea may vary on annual time scales and highlights the importance of repeated GEOTRACES sections.Plain Language Summary This study presents new results of thorium isotopes from the central Arctic Ocean. Thorium-230 is produced continuously in seawater by radioactive decay of 234 U and subsequently removed by particle scavenging. We show that observed changes in 230 Th concentrations compared to earlier times are related to submarine volcanic eruptions. We use 230 Th data from three different expeditions conducted in 1991, 2007, and 2015. The Nansen Basin is part of the Eurasian Basin of the Arctic Ocean. It is divided from the Amundsen Basin by the Gakkel Ridge. The Gakkel Ridge is a region where the Eurasian and the North American plates spread apart, triggering volcanism. Submarine volcanos and hydrothermal vents release trace elements such as iron. Iron is known to be oxidized to particles that react with 230 Th. Thus, when iron particles sink they remove 230 Th from the water column. In the Nansen Basin this process took place between 2007 and 2015, triggered by earthquake-induced volcanic eruptions in 2001. In this study, we present a conceptual hydrothermal scavenging process and plume dispersal by deep water circulation.