Beschreibung: 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 This publication provides the critical reference for unpublished data, as well as for studies that make use of a large cross-section of data from the IDP2017.

Beschreibung: The orbital-scale timing of South Asian monsoon (SAM) precipitation is poorly understood. Here we present new SST and seawater δ18O (δ18Osw) records from the Bay of Bengal, the core convective region of the South Asian monsoon, over the past 1 million years. Our records reveal that SAM precipitation peaked in the precession band ~9 kyrs after Northern Hemisphere summer insolation maxima, in phase with records of SAM winds in the Arabian Sea and eastern Indian Ocean. Precession-band variance, however, accounts for ~30% of the total variance of SAM precipitation while it was either absent or dominant in records of the East Asian monsoon (EAM). This and the observation that SAM precipitation was phase locked with obliquity minima and was sensitive to Southern Hemisphere warming provides clear evidence that SAM and EAM precipitation responded differently to orbital forcing and highlights the importance of internal processes forcing monsoon variability.

Beschreibung: Seawater rare earth element (REE) concentrations are increasingly applied to reconstruct water mass histories by exploiting relative changes in the distinctive normalised patterns. However, the mechanisms by which water masses gain their patterns are yet to be fully explained. To examine this, we collected water samples along the Extended Ellett Line (EEL), an oceanographic transect between Iceland and Scotland, and measured dissolved REE by offline automated chromatography (SeaFAST) and ICP-MS. The proximity to two continental boundaries, the incipient spring bloom coincident with the timing of the cruise, and the importance of deep water circulation in this climatically sensitive gateway region make it an ideal location to investigate sources of REE to seawater and the effects of vertical cycling and lateral advection on their distribution. The deep waters have REE concentrations closest to typical North Atlantic seawater and are dominated by lateral advection. Comparison to published seawater REE concentrations of the same water masses in other locations provides a first measure of the temporal and spatial stability of the seawater REE signal. We demonstrate the REE pattern is replicated for Iceland-Scotland Overflow Water (ISOW) in the Iceland Basin from adjacent stations sampled 16 years previously. A recently published Labrador Sea Water (LSW) dissolved REE signal is reproduced in the Rockall Trough but shows greater light and mid REE alteration in the Iceland Basin, possibly due to the dominant effect of ISOW and/or continental inputs. An obvious concentration gradient from seafloor sediments to the overlying water column in the Rockall Trough, but not the Iceland Basin, highlights release of light and mid REE from resuspended sediments and pore waters, possibly a seasonal effect associated with the timing of the spring bloom in each basin. The EEL dissolved oxygen minimum at the permanent pycnocline corresponds to positive heavy REE enrichment, indicating maximum rates of organic matter remineralisation and associated REE release. We tentatively suggest a bacterial role to account for the observed heavy REE deviations. This study highlights the need for fully constrained REE sources and sinks, including the temporary nature of some sources, to achieve a balanced budget of seawater REE.

Beschreibung: Highlights • High lithogenic input in surface waters in the Panama Basin results in radiogenic εNd of up to +4.3. • Radiogenic Nd derived from particles can reset the Nd IC of water masses within time scales years. • Lithogenic input of REEs and corresponding Nd IC in surface waters are seasonally influenced. The distribution of dissolved rare earth elements (REEs) and neodymium isotopes (εNd) in the open ocean traces water mass mixing and provides information on lithogenic inputs to the source regions of the water masses. However, the processes influencing the REE budget at the ocean margins, in particular source and sink mechanisms, are not yet well quantified. In this study the first dissolved REE concentrations and Nd isotope compositions of seawater from the Panama Basin (RV Meteor cruise M90) in the Eastern Equatorial Pacific (EEP) are presented. The EEP is characterized by one of the world's largest oxygen minimum zones (OMZs). It is dominated by high particle fluxes that are expected to enhance the removal of REEs from the water column by scavenging. The measured REE concentrations peak at the surface indicating high lithogenic input, which is supported by shale-normalized REE patterns in surface waters and highly radiogenic εNd signatures ranging between +1.4 and +4.3, the latter value constituting the most radiogenic value measured for seawater to date. In contrast, intermediate and deep water REE concentrations are low compared to other Pacific Basins and suggest enhanced removal via scavenging associated with high particle fluxes. The εNd signatures of intermediate and deep waters are less radiogenic than surface waters ranging between −1.4 and +1.3 but significantly more radiogenic than source water masses in the EEP. The εNd signatures consequently do not reflect mixing of intermediate and deep water masses entering the Panama Basin but can only be explained by lithogenic inputs originating from source rocks with highly radiogenic Nd isotope signatures such as the Central American Volcanic Arc (εNd=+3 to +10). Our data demonstrate significant surface input via continental particles, which are partially dissolved in the water column and thereby release REEs and particularly radiogenic Nd isotope signatures to the subsurface ocean. Data obtained from a re-occupied station in the southern Panama Basin for the first time shows that these processes can partially reset water mass Nd isotope and REE signatures of the entire water column proximal to continental sources on time scales of a few years.

Beschreibung: Past ocean temperatures and salinities can be approximated from combined stable oxygen isotopes (δ18O) and Mg ∕ Ca measurements in fossil foraminiferal tests with varying success. To further refine this approach, we collected living planktic foraminifers by net sampling and pumping of sea surface water from the Caribbean Sea, the eastern Gulf of Mexico and the Florida Straits. Analyses of δ18O and Mg ∕ Ca in eight living planktic species (Globigerinoides sacculifer, Orbulina universa, Neogloboquadrina dutertrei, Pulleniatina obliquiloculata, Globorotalia menardii, Globorotalia ungulata, Globorotalia truncatulinoides and Globorotalia tumida) were compared to measured in situ properties of the ambient seawater (temperature, salinity and δ18Oseawater) and fossil tests of underlying surface sediments. “Vital effects” such as symbiont activity and test growth cause δ18O disequilibria with respect to the ambient seawater and a large scatter in foraminiferal Mg ∕ Ca. Overall, ocean temperature is the most prominent environmental influence on δ18Ocalcite and Mg ∕ Ca. Enrichment of the heavier 18O isotope in living specimens below the mixed layer and in fossil tests is clearly related to lowered in situ temperatures and gametogenic calcification. Mg ∕ Ca-based temperature estimates of G. sacculifer indicate seasonal maximum accumulation rates on the seafloor in early spring (March) at Caribbean stations and later in the year (May) in the Florida Straits, related to the respective mixed layer temperatures of ∼26 ∘C. Notably, G. sacculifer reveals a weak positive linear relationship between foraminiferal derived δ18Oseawater estimates and both measured in situ δ18Oseawater and salinity. Our results affirm the applicability of existing δ18O and Mg ∕ Ca calibrations for the reconstruction of past ocean temperatures and δ18Oseawater reflecting salinity due to the convincing accordance of proxy data in both living and fossil foraminifers, and in situ environmental parameters. Large vital effects and seasonally varying proxy signals, however, need to be taken into account.

Beschreibung: Highlights • First comprehensive seawater Nd isotope and REE data for the Laptev Sea. • Dissolved Nd isotopes, salinity and stable oxygen isotopes trace water masses. • No evidence for REE release from particles of the organic-rich Siberian Rivers. • Preferential estuarine LREE removal follows increasing salinity from 10 to 34. • Formation and melting of sea ice redistribute REEs within water column. Abstract Marine neodymium (Nd) isotope and rare earth element (REE) compositions are valuable tracers for present and past ocean circulation and continental inputs. Yet their supply via high latitude estuaries is largely unknown. Here we present a comprehensive dissolved Nd isotope (expressed as εNd values) and REE data set together with seawater stable oxygen isotope ( O) compositions of samples from the Laptev Sea recovered in two Arctic summers and one winter. The Laptev Sea is a shallow Siberian Shelf sea characterized by extensive river-runoff, sea-ice production and ice transport into the Arctic Ocean. The large variability in εNd (−6 to −17), REE concentrations (16 to 600 pmol/kg for Nd) and REE patterns is controlled by freshwater supply from distinct riverine sources and open ocean Arctic Atlantic Water. Strikingly and contrary to expectations, except for cerium no evidence for significant release of REEs from particulate phases is found, which is attributed to low amounts of suspended particulate matter and high dissolved organic carbon concentrations present in the contributing rivers. Essentially all shelf waters are depleted in light (L)REEs, while the distribution of the heavy REEs shows a deficiency at the surface and a pronounced excess in the bottom layer. This distribution is consistent with REE removal through coagulation of riverine nanoparticles and colloids starting at salinities near 10 and resulting in a drop of all REE concentrations by ∼30%. With increasing salinity preferential LREE removal is observable reaching ∼75% for Nd at a salinity of 34. Although the delayed onset of dissolved REE removal contrasts with most previous observations from other estuarine environments, it agrees remarkably well with results from recent experiments simulating estuarine mixing of seawater with organic-rich river waters. In addition, melting and formation of sea ice leads to further REE depletion at the surface and strong REE enrichment near the shelf bottom as a function of ice melting and brine transfer, respectively. The ice-related processes significantly affect the distribution of dissolved REEs in high-latitude estuaries and likely also similarly contribute to the redistribution of other dissolved seawater constituents.

Beschreibung: The quantitative reconstruction of past seawater salinity has yet to be achieved and the search for a direct and independent salinity proxy is ongoing. Recent culture and field studies show a significant positive correlation of Na/Ca with salinity in benthic and planktonic foraminiferal calcite. For accurate paleoceanographic reconstructions, consistent and reliable calibrations are necessary, which are still missing. In order to assess the reliability of foraminiferal Na/Ca as a direct proxy for seawater salinity, this study presents electron microprobe Na/Ca data, measured on cultured specimens of Trilobatus sacculifer. The culture experiments were conducted over a wide salinity range of 26 to 45, while temperature was kept constant. To further understand potential controlling factors of Na incorporation, measurements were also performed on foraminifera cultured at various temperatures in the range of 19.5 °C to 29.5 °C under constant salinity conditions. Foraminiferal Na/Ca ratios positively correlate with seawater salinity (Na/Caforam = 0.97 + 0.115 ⋅ Salinity, R = 0.97, p 〈 0.005). Temperature on the other hand exhibits no statistically significant relationship with Na/Ca ratios indicating salinity to be the dominant factor controlling Na incorporation. The culturing results are corroborated by measurements on T. sacculifer from Caribbean and Gulf of Guinea surface sediments. In conclusion, planktonic foraminiferal Na/Ca can be applied as a reliable proxy for reconstructing sea surface salinities, albeit species-specific calibrations might be necessary.

Beschreibung: This study investigates chromium isotope variations (δ53Cr) and REE patterns in present-day biogenic carbonates and ocean waters from Lady Elliot Island (LEI) located in the southern Great Barrier Reef (GBR), Australia, which is one of the world's largest carbonate-producing shelf ecosystems. Our results from thoroughly cleaned biogenic carbonates collected at LEI, with no detectable evidence for lithogenic Cr and/or Mn–Fe oxide coating contamination, revealed a systematic and statistically significant correlation (r2=0.83, p〈0.05) between δ53Cr and cerium anomaly (Ce/Ce*) data in molluscan shells (i.e., gastropods). This in turn implies a redox-controlled incorporation of Cr from seawater into a shell during mineralization mediated by the organism. In particular, shells with higher δ53Cr values, which approach the Cr isotope composition of local seawater, tend to be associated with more negative Ce/Ce*. Importantly, the intercept of the above δ53Cr vs. Ce/Ce* correlation points to the Cr isotope composition of local ocean water, which has an average δ53Cr of +0.82±0.13‰ (2σ relative to SRM 979). These findings thus indicate that the above multi-proxy approach could be used to reconstruct the δ53Cr signature of local paleo-seawater based on Ce/Ce* and δ53Cr data in a set of well-preserved fossil skeletal carbonates (i.e., molluscan shells) collected at a specific site. Interestingly, the only calcifying organism from LEI that yielded identical δ53Cr vs. Ce/Ce* values as those in ambient ocean water was a microbial calcitic carbonate produced by red coralline algae (Lithothamnion sp.). This organism thus seems to incorporate Cr isotopes and REE from seawater without additional biological discrimination and/or isotope fractionation effects. Considering that calcite is a more stable CaCO3 polymorph during post-depositional alternation and diagenetic stabilization of marine carbonates (compared to aragonite), the fossil counterparts of these algal-microbial carbonates (microbialites) might thus represent ideal natural archives of the paleo-seawater δ53Cr and Ce/Ce* variations over geological time. Finally, our compilation of δ53Cr data from recent marine biogenic carbonates originating from the main oceanic provinces (South/North Pacific, South/North Atlantic, Caribbean, Mediterranean Sea) confirms that marine carbonates tend to be systematically enriched in light Cr isotopes relative to local ocean waters. Trace element constraints, however, indicate that some of these shifts to lower δ53Cr values (i.e., approaching −0.1 per mil) are related to a presence of lithogenic Cr in the shells, causing a diagenetic overprint of the primary marine δ53Cr signal.

Beschreibung: Highlights • We present a Ba isotope data set of seawater, river waters and biogenic particles. • Ba isotope signatures of upper ocean waters are heavier than river and deep waters. • Adsorption of lighter Ba isotopes on biogenic particles induces the fractionation. • Ba isotopes trace land–sea interactions and ocean mixing processes. • Decoupling of Ba from major nutrients confirms Ba to be a biointermediate element. Abstract The distribution of barium (Ba) concentrations in seawater resembles that of nutrients and Ba has been widely used as a proxy of paleoproductivity. However, the exact mechanisms controlling the nutrient-like behavior, and thus the fundamentals of Ba chemistry in the ocean, have not been fully resolved. Here we present a set of full water column dissolved Ba (DBa) isotope (δ137BaDBa) profiles from the South China Sea and the East China Sea that receives large freshwater inputs from the Changjiang (Yangtze River). We find pronounced and systematic horizontal and depth dependent δ137BaDBa gradients. Beyond the river influence characterized by generally light signatures (0.0 to +0.3‰+0.3‰), the δ137BaDBa values in the upper water column are significantly higher (+0.9‰+0.9‰) than those in the deep waters (+0.5‰+0.5‰). Moreover, δ137BaDBa signatures are essentially constant in the entire upper 100 m, in which dissolved silicon isotopes are fractionated during diatom growth resulting in the heaviest isotopic compositions in the very surface waters. Combined with the decoupling of DBa concentrations and δ137BaDBa from the concentrations of nitrate and phosphate this implies that the apparent nutrient-like fractionation of Ba isotopes in seawater is primarily induced by preferential adsorption of the lighter isotopes onto biogenic particles rather than by biological utilization. The subsurface δ137BaDBa distribution is dominated by water mass mixing. The application of stable Ba isotopes as a proxy for nutrient cycling should therefore be considered with caution and both biological and physical processes need to be considered. Clearly, however, Ba isotopes show great potential as a new tracer for land–sea interactions and ocean mixing processes.

Beschreibung: One of the key activities during the initial phase of the international GEOTRACES program was an extensive international intercalibration effort, to ensure that results for a range of trace elements and isotopes (TEIs) from different cruises and from different laboratories can be compared in a meaningful way. Here we present the results from the intercalibration efforts on neodymium isotopes and rare earth elements in seawater and marine particles. Fifteen different laboratories reported results for dissolved 143Nd/144Nd ratios in seawater at three different locations (BATS 15 m, BATS 2000 m, SAFe 3000 m), with an overall agreement within 47 to 57 ppm (2σ standard deviation of the mean). A similar agreement was found for analyses of an unknown pure Nd standard solution carried out by 13 laboratories (56 ppm), indicating that mass spectrometry is the main variable in achieving accurate and precise Nd isotope ratios. Overall, this result is very satisfactory, as the achieved precision is a factor of 40 better than the range of Nd isotopic compositions observed in the global ocean. Intercalibration for dissolved rare earth element concentrations (REEs) by six laboratories for two water depths at BATS yielded a reproducibility of 15% or better for all REE except Ce, which seems to be the most blank-sensitive REE. Neodymium concentrations from 12 laboratories show an agreement within 9%, reflecting the best currently possible reproducibility. Results for Nd isotopic compositions and REE concentrations on marine particles are inconclusive, and should be revisited in the future.