Description: The GEOTRACES Intermediate Data Product 2017 (IDP2017) is the second publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2016. The IDP2017 includes data from the Atlantic, Pacific, Arctic, Southern and Indian oceans, with about twice the data volume of the previous IDP2014. For the first time, the IDP2017 contains data for a large suite of biogeochemical parameters as well as aerosol and rain data characterising atmospheric trace element and isotope (TEI) sources. The TEI data in the IDP2017 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at crossover stations. The IDP2017 consists of two parts: (1) a compilation of digital data for more than 450 TEIs as well as standard hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing an on-line atlas that includes more than 590 section plots and 130 animated 3D scenes. The digital data are provided in several formats, including ASCII, Excel spreadsheet, netCDF, and Ocean Data View collection. Users can download the full data packages or make their own custom selections with a new on-line data extraction service. In addition to the actual data values, the IDP2017 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering and for statistical analysis. Metadata about data originators, analytical methods and original publications related to the data are linked in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2017 as section plots and rotating 3D scenes. The basin-wide 3D scenes combine data from many cruises and provide quick overviews of large-scale tracer distributions. These 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of tracer plumes near ocean margins or along ridges. The IDP2017 is the result of a truly international effort involving 326 researchers from 22 countries. This publication provides the critical reference for unpublished data, as well as for studies that make use of a large cross-section of data from the IDP2017.

Description: The Labrador Sea is one of the key areas for deep water formation driving the Atlantic thermohaline circulation and thus plays an important role in Northern Hemisphere climatic fluctuations. In order to better constrain the overturning processes and the origins of the distinct water masses, combined dissolved Hf–Nd isotopic compositions and rare earth element (REE) distribution patterns were obtained from four water depth profiles along a section across the Labrador Sea. These were complemented by one surface sample off the southern tip of Greenland, three shallow water samples off the coast of Newfoundland, and two deep water samples off Nova Scotia. Although light REEs are markedly enriched in the surface waters off the coast of Newfoundland compared to north Atlantic waters, the REE concentration profiles are essentially invariant throughout the water column across the Labrador Sea. The hafnium concentrations of surface waters exhibit a narrow range between 0.6 and 1 pmol/kg but are not significantly higher than at depth. Neodymium isotope signatures (ɛNd) vary from unradiogenic values between −16.8 and −14.9 at the surface to more radiogenic values near −11.0 at the bottom of the Labrador Sea mainly reflecting the advection of the Denmark Strait Overflow Water and North East Atlantic Deep Water, the signatures of which are influenced by weathering contributions from Icelandic basalts. Unlike Nd, water column radiogenic Hf isotope signatures (ɛHf) are more variable representing diverse weathering inputs from the surrounding landmasses. The least radiogenic seawater ɛHf signatures (up to −11.7) are found in surface waters close to Greenland and near the Canadian margin. This reflects the influence of recirculating Irminger Current Waters, which are affected by highly unradiogenic inputs from Greenland. A three to four ɛHf unit difference is observed between Denmark Strait Overflow Water (ɛHf ∼ −4) and North East Atlantic Deep Water (ɛHf ∼ −0.1), although their source waters have essentially the same ɛNd signature. This most likely reflects different weathering signals of hafnium delivered to Denmark Strait Overflow Water and North East Atlantic Deep Water (incongruent weathering of old rocks from Greenland versus basaltic rocks from Iceland). In addition, the ɛHf data resolve two layers within the main body of Labrador Sea Water not visible in the ɛNd distribution, which are shallow Labrador Sea Water (ɛHf ∼ −2) and deep Labrador Sea Water (ɛHf ∼ −4.5). The latter layer was formed between the late 1980’s and mid 1990’s during the last cold state of the Labrador Sea and underwent substantial modification since its formation through the admixture of Irminger Water, Iceland Slope Water and North East Atlantic Deep Water, which is reflected in its less radiogenic ɛHf signature. The overall behavior of Hf in the water column suggests its higher sensitivity to local changes in weathering inputs on annual to decadal timescales. Although application of Hf isotopes as a tracer for global water mass mixing is complicated by their susceptibility to incongruent weathering inputs they are a promising tracer of local processes in restricted basins such as the Labrador Sea.

Description: Radiogenic isotopes of hafnium (Hf) and neodymium (Nd) are powerful tracers for water mass transport and trace metal cycling in the present and past oceans. However, due to the scarcity of available data the processes governing their distribution are not well understood. Here we present the first combined dissolved Hf and Nd isotope and concentration data from surface waters of the Atlantic sector of the Southern Ocean. The samples were collected along the Zero Meridian, in the Weddell Sea and in the Drake Passage during RV Polarstern expeditions ANTXXIV/3 and ANTXXIII/3 in the frame of the International Polar Year (IPY) and the GEOTRACES program. The general distribution of Hf and Nd concentrations in the region is similar. However, at the northernmost station located 200 km southwest of Cape Town a pronounced increase of the Nd concentration is observed, whereas the Hf concentration is minimal, suggesting much less Hf than Nd is released by the weathering of the South African Archean cratonic rocks. From the southern part of the Subtropical Front (STF) to the Polar Front (PF) Hf and Nd show the lowest concentrations (〈0.12 pmol/kg and 10 pmol/kg, respectively), most probably due to the low terrigenous flux in this area and efficient scavenging of Hf and Nd by biogenic opal. In the vicinity of landmasses the dissolved Hf and Nd isotope compositions are clearly labeled by terrigenous inputs. Near South Africa Nd isotope values as low as εNd = −18.9 indicate unradiogenic inputs supplied via the Agulhas Current. Further south the isotopic data show significant increases to εHf = 6.1 and εNd = −4.0 documenting exchange of seawater Nd and Hf with the Antarctic Peninsula. In the open Southern Ocean the Nd isotope compositions are relatively homogeneous (εNd ∼ −8 to −8.5) towards the STF, within the Antarctic Circumpolar Current, in the Weddell Gyre, and the Drake Passage. The Hf isotope compositions in the entire study area only show a small range between εHf = + 6.1 and +2.8 support Hf to be more readily released from young mafic rocks compared to old continental ones. The Nd isotope composition ranges from εNd = −18.9 to −4.0 showing Nd isotopes to be a sensitive tracer for the provenance of weathering inputs into surface waters of the Southern Ocean.

Description: It is well established that Hf weathers incongruently such that the isotopic compositions in seawater are offset from those of Nd relative to the correlation defined by bulk lithologies of the continental crust. Here we study this process in detail with new records of the seasonal variability of isotope compositions and concentrations of Hf and Nd in four Swiss rivers. The water has been filtered at a pore size of 0.45 mu m and therefore represents the truly dissolved and the colloidal pool of both elements. The studied rivers drain metamorphic (gneissic) or sedimentary (mixed carbonate/siliciclastic) lithologies. The dissolved isotope data are compared to the isotope compositions and concentrations of the suspended load and different fractions of the actual source rocks in the respective catchments, as well as to concomitant changes in the aqueous chemistry of the major elements. Dissolved Nd concentrations span similar ranges for all rivers, whereas Hf concentrations are one order of magnitude lower in the rivers that drain gneissic catchments compared to those draining sedimentary rocks. This primarily results from the retention of most of the Hf in the gneissic zircons, as indicated by the Hf budget of the gneisses, whereas Hf in the sedimentary catchments is readily weathered from fine detrital silicates. Large differences are found between the dissolved Hf isotope compositions of the rivers and those of the suspended load and the source rocks, consistent with the release of Hf from a radiogenic rock fraction during weathering. In the metamorphic catchments this primarily reflects that fact that zircons are barely accessible for weathering. The zircon-free portion of the rocks appears to weather congruently as the riverine Hf isotope compositions are similar to the zircon-free portion of the gneisses, rather than being distinctly more radiogenic. Leaching experiments performed to understand the riverine Hf budget in the sedimentary catchments reveal that the carbonate fraction of the sedimentary rocks is extremely radiogenic, yielding Hf isotope compositions up to epsilon(Hf) of + 208. However, the Hf concentrations in the carbonate fractions are too low to dominate the riverine Hf budget, which is instead controlled by the weathering of detrital silicate minerals. Two of the catchments, a metamorphic and a sedimentary one, show relatively systematic changes towards more radiogenic dissolved Hf isotope compositions as discharge increases. This suggests that continental runoff conditions could be a relevant parameter for the control of the seawater Hf isotope composition, whereby more congruent weathering is achieved during low discharge when Hf is increasingly derived from weathering-resistant unradiogenic minerals

Description: The fractionation of silicon (Si) stable isotopes by biological activity in the surface ocean makes the stable isotope composition of silicon (δ30Si) dissolved in seawater a sensitive tracer of the oceanic biogeochemical Si cycle. We present a high-precision dataset that characterizes the δ30Si distribution in the deep Atlantic Ocean from Denmark Strait to Drake Passage, documenting strong meridional and smaller, but resolvable, vertical δ30Si gradients. We show that these gradients are related to the two sources of deep and bottom waters in the Atlantic Ocean: waters of North Atlantic and Nordic origin carry a high δ30Si signature of ≥+1.7‰ into the deep Atlantic, while Antarctic Bottom Water transports Si with a low δ30Si value of around +1.2‰. The deep Atlantic δ30Si distribution is thus governed by the quasi-conservative mixing of Si from these two isotopically distinct sources. This disparity in Si isotope composition between the North Atlantic and Southern Ocean is in marked contrast to the homogeneity of the stable nitrogen isotope composition of deep ocean nitrate (δ15N-NO3). We infer that the meridional δ30Si gradient derives from the transport of the high δ30Si signature of Southern Ocean intermediate/mode waters into the North Atlantic by the upper return path of the meridional overturning circulation (MOC). The basin-scale deep Atlantic δ30Si gradient thus owes its existence to the interaction of the physical circulation with biological nutrient uptake at high southern latitudes, which fractionates Si isotopes between the abyssal and intermediate/mode waters formed in the Southern Ocean. Key Points: - Deep Atlantic Ocean displays gradient in Si isotopic composition of silicic acid - The gradient is caused by quasi-conservative mixing of Si from NADW and AABW - Contrasting isotope signature of NADW and AABW due to interaction of biology and MOC

Description: Highlights: • Nd and Hf are released from sediments to the water column in the Amundsen Sea Embayment. • Seawater Nd and Hf isotope compositions show opposed trends close to the Marie Byrd Seamounts. • AABW is isotopically distinct in Nd between the Atlantic and the Pacific sectors. • Hf isotope variations occur between the sectors, but not with depth in each sector. Abstract: Neodymium and hafnium isotopes and elemental concentrations (Sm, Nd, Hf, Zr) have been measured in three water column profiles south of the Antarctic Circumpolar Current in, and to the east of the Ross Sea, in conjunction with five bottom water samples from the Amundsen Sea Embayment. Neodymium and hafnium both appear to be released from sediments in the Embayment. In the case of Nd, this is reflected in radiogenic isotope compositions (εNdεNd up to −5.4) and highly elevated concentrations (up to 41 pmol/kg). Hafnium isotopes, on the other hand, are only very slightly altered relative to the open ocean sites, and boundary release is most prominently indicated by elevated concentrations (〉1 pmol/kg versus ∼0.7 pmol/kg). There is also a local input of both Hf and Nd at the Marie Byrd Seamounts, which leads to Nd isotope compositions as radiogenic as −3.1, and hafnium shifted to less radiogenic compositions in local bottom water. A compilation of the new data with literature data reveals a consistent view of the influence of Antarctica on the Nd isotope composition in Lower Circumpolar Deep Water (LCDW) and Antarctic Bottom Water (AABW). Sector specific Nd addition shifts AABW formed in the Atlantic sector to less radiogenic isotope compositions (average εNd=−9εNd=−9) relative to LCDW (average εNd=−8.4εNd=−8.4), whereas AABW in the Pacific sector is shifted to more radiogenic values (average εNd=−7εNd=−7). The evolution towards more radiogenic εNdεNd with depth in LCDW in the Pacific sector is likely to reflect admixture of AABW but, in addition, is also controlled by boundary exchange with the slope as observed at the Marie Byrd Seamounts. Hafnium isotopes are relatively homogeneous in the data set, ranging between εHf=+2εHf=+2 and +3.8 for most samples, excluding less radiogenic compositions in deep waters close to the Marie Byrd Seamounts. The Hf isotope composition in the Pacific sector is, however, slightly less radiogenic than in the Atlantic, corresponding to an average of +3 relative to an average of +3.8. This probably reflects unradiogenic Hf inputs from Antarctica to the Pacific sector, which are vertically homogenized by reversible scavenging. The Hf isotope heterogeneity in LCDW between both sectors is likely to indicate a shorter seawater residence time for Hf than for Nd, which is consistent with the dissolved – particulate phase partitioning of both elements.

Description: Combined seawater radiogenic hafnium (Hf) and neodymium (Nd) isotope compositions were extracted from bulk sediment leachates and foraminifera of Site 1088, ODP Leg 177, 2082 m water depth on the Agulhas Ridge. The new data provide a continuous reconstruction of long and short-term changes in ocean circulation and continental weathering inputs since the Mid-Miocene. Due to its intermediate water depth the sediments of this core sensitively recorded changes in admixture of North Atlantic Deep Water (NADW) to the Antarctic Circumpolar Current (ACC) as a function of the strength of the Atlantic Meridional Overturning Circulation (AMOC). Nd isotope compositions (εNd) range from -7 to -11 with glacial values generally 1 to 3 units more radiogenic than during the interglacials of the Quaternary. The data reveal episodes of significantly increased AMOC strength during late Miocene and Pliocene warm periods whereas peak radiogenic εNd values mark a strongly diminished AMOC during the major intensification of Northern Hemisphere Glaciation near 2.8 Ma and in the Pleistocene after 1.5 Ma. In contrast, the Hf isotope compositions (εHf) show an essentially continuous evolution from highly radiogenic values of up to +11 during the Miocene to less radiogenic present day values (+2 to +4) during the late Quaternary. The data document a long-term transition in dominant weathering inputs, where inputs from the South America are replaced by those from Southern Africa. Moreover, radiogenic peaks provide evidence for the supply of radiogenic Hf originating from Patagonian rocks to the Atlantic sector of the Southern Ocean via dust inputs.

Description: AB: Radiogenic hafnium (Hf) and neodymium (Nd) isotopes have been used as tracers for past continental weathering regimes and ocean circulation. To date there is only very few data available on dissolved Hf and Nd isotope compositions of the modern Southern Ocean (SO). During expedition ANTXXIV/3 (February to April 2008) filtered (0.45 µm) seawater samples (20-120 liters) were collected in the Drake Passage, the Weddell Sea and the Subantarctic Atlantic Ocean (near the Zero Meridian) to determine the dissolved isotopic composition of Hf and Nd of the major water masses in the SO. The dissolved seawater isotopic compositions of both Hf and Nd in the open Drake Passage show only minor variability (εHf = 4.2 to 4.7 and εNd = -8.8 to -7.6). However, in the Weddell Sea and at stations from the southernmost part of the Drake Passage close to the Antarctic Peninsula, the Nd isotopic composition ranged from εNd = -8.9 to -6.4. At one station near the Subtropical Convergence we measuered εNd = -15.9 in surface waters and -8.9 and -9.9 in intermediate and deep waters, respectively. Compared with the previously measured particulate fraction, the dissolved Nd isotope distribution indicates that particle leaching contributes unradiogenic Nd to near surface waters, whereas the isotopic compositions of deep waters are controlled by water mass mixing. Furthermore, we infer that the Nd isotope signature of Antarctic Intermediate Water (AAIW), which is formed in the Polar Frontal Zone, has been mixed with relatively unradiogenic surface water signatures before it is subducted. Our data therefore suggest that the variability of the surface water Nd isotope composition is relevant for the final Nd isotope signature of the submerging intermediate waters in the SO.

Description: The marine chromium (Cr) cycle is still insufficiently understood, in particular the mechanisms modulating the spatial distribution of dissolved stable Cr isotopes in seawater. Redox transformations between its main oxidation states, Cr(VI) and Cr(III), have been held accountable for the observed tight inverse logarithmic relationship between the dissolved Cr concentration [Cr] and its isotopic composition (δ53Cr), whereby isotopically light Cr(III) is removed in surface waters and oxygen minimum zones (OMZs), and subsequently released to deeper waters from remineralized particles or sediments. Seawater [Cr] and δ53Cr were investigated in a series of depth profiles across the Peruvian margin OMZ, covering a wide spectrum of dissolved oxygen concentrations ranging from 2 to 242 µmol/kg. We found [Cr] ranging from 1.5 to 5.5 nmol/kg, associated with δ53Cr variations between +1.59 and +0.72 ‰, but no systematic relationship to dissolved oxygen concentrations. However, distinctly different seawater profiles were observed above the suboxic/anoxic shelf compared to those located further offshore, with substantial Cr removal restricted to suboxic or anoxic environments on the shelf. This suggests that suboxic conditions ([O2] 〈 5 µmol/kg) alone are not sufficient to account for substantial Cr removal. Given that environmental conditions under which Cr can be reduced remain restricted spatially, the role of this sink in the marine Cr cycle may therefore be small. Additionally, some observations corroborate the assumption that Cr reduction is not necessarily accompanied by immediate adsorption of the formed Cr(III) onto particles, leading to its removal from the dissolved phase. Instead, partial removal of Cr(III) via particles, leaving a residual dissolved Cr(III) pool, may be more widespread in suboxic waters.

Description: The ratio of atmosphere-derived 10 Be to continent-derived 9 Be in marine sediments has been used to probe the long-term relationship between continental denudation and climate. However, its application is complicated by uncertainty in 9 Be transfer through the land-ocean interface. The riverine dissolved load alone is insufficient to close the marine 9 Be budget, largely due to substantial removal of riverine 9 Be to continental margin sediments. We focus on the ultimate fate of this latter Be. We present sediment pore-water Be profiles from diverse continental margin environments to quantify the diagenetic Be release to the ocean. Our results suggest that pore-water Be cycling is mainly controlled by particulate supply and Mn-Fe cycling, leading to higher benthic fluxes on shelves. Benthic fluxes may help close the 9 Be budget and are at least comparable to, or higher (~2-fold) than, the riverine dissolved input. These observations demand a revised model framework, which considers the potentially dominant benthic source, to robustly interpret marine Be isotopic records.