Description: The strength of the North Atlantic Meridional Overturning Circulation during climatically highly variable Marine Isotope Stage (MIS) 3 has attracted much attention in recent years. Here we present highresolution Nd isotope compositions of past seawater derived from authigenic Fe-Mn oxyhydroxides recovered from drift sediments on the Blake Ridge in the deep western North Atlantic (ODP Leg 172, Site 1060, 3481 m water depth). The data cover the period from 45 to 35 ka BP, tracing circulation changes during major Heinrich iceberg discharge event 4 (H4, ~40-39kaBP), The Nd isotope record suggests that there was no northern source water (NSW) mass like modern NADW at the deeper part of Blake Ridge at any time between 45 and 35 ka. This is fundamentally different from the hydrographic situation during the Holocene where NADW extends below 4500 m at this location. The εNd of past deep water recorded in the Blake Ridge sediments was least radiogenic during Dansgaard/Oeschger (D/O) Interstadial (IS) 8 (εNd = -11.3)and most radiogenic immediately preceding IS 9 (εNd = -9.8). More radiogenic compositions were also recorded during H4 (-10.2 ≤ εNd ≤ 9.9). The Nd isotope variability in MIS 3 matches that of a physical bottom current strength reconstruction from the same location. Neither record follows the pattern of Northern Hemisphere D/O climatic cycles. In our record, reduced mixing with northern source waters started in stadial 12 and lasted until after H4 in stadial 9, followed by a rapid increase in NSW contribution thereafter. This major change in the Nd isotope record predates the iceberg discharge event Heinrich 4 by more than 3 ka indicating a shallowing of the water mass boundary between Glacial North Atlantic Intermediate Water and Southern Source Water beneath. This early change in bottom water properties at the deep Blake Ridge suggests that North Atlantic deep water advection may already have decreased several thousand years before the actual iceberg discharge event and associated freshening of the surface waters in the North Atlantic. The change can thus not be attributed to climatic events in the North Atlantic but may be related to changes in flux of deep water from the South.

Description: The marine iodine cycle has significant impacts on air quality and atmospheric chemistry. Specifically, the reaction of iodide with ozone in the top few micrometres of the surface ocean is an important sink for tropospheric ozone (a pollutant gas) and the dominant source of reactive iodine to the atmosphere. Sea surface iodide parameterisations are now being implemented in air quality models, but these are currently a major source of uncertainty. Relatively little observational data is available to estimate the global surface iodide concentrations, and this data has not hitherto been openly available in a collated, digital form. Here we present all available sea surface (〈20 m depth) iodide observations. The dataset includes values digitised from published manuscripts, published and unpublished data supplied directly by the originators, and data obtained from repositories. It contains 1342 data points, and spans latitudes from 70°S to 68°N, representing all major basins. The data may be used to model sea surface iodide concentrations or as a reference for future observations.

Description: In this study, we used stable isotopes of oxygen (δ18O), deuterium (δD), and dissolved inorganic carbon (δ13CDIC) in combination with temperature, salinity, oxygen and nutrient concentrations to characterize the coastal (71-78 °W) and an oceanic (82-98 °W) water masses (SAAW-Subantarctic Surface Water; STW-Subtropical Water; ESSW-Equatorial Subsurface water; AAIW-Antarctic Intermediate Water; PDW-Pacific Deep Water) of the Southeast Pacific (SEP). The results show that δ18O and δD can be used to differentiate between SAAW-STW, SAAW-ESSW and ESSW-AAIW. δ13CDIC signatures can be used to differentiate between STW-ESSW (oceanic section), SAAW-ESSW, ESSW-AAIW and AAIW-PDW. Compared with the oceanic section, our new coastal section highlights differences in both the chemistry and geometry of water masses above 1000 m. Previous paleoceanographic studies using marine sediments from the SEP continental margin used the present-day hydrological oceanic transect to compare against, as the coastal section was not sufficiently characterized. We suggest that our new results of the coastal section should be used for past characterizations of the SEP water masses that are usually based on continental margin sediment samples.

Description: Planktic and benthic foraminiferal iodine (I) to calcium (Ca) molar ratios have been proposed as an exciting new proxy to assess subsurface and bottom water oxygenation in the past. Compared to trace metals, the analysis of iodine in foraminiferal calcite is more challenging, as iodine is volatile in acid solution. Here, we compare previous analyses that use tertiary amine with alternative analyses using tetramethylammonium hydroxide (TMAH) and ammonium hydroxide (NH4OH) to stabilize iodine in solution. In addition, we assess the effect of sample size and cleaning on planktic and benthic foraminiferal I/Ca. Our stabilization experiments with TMAH and NH4OH show similar trends as those using tertiary amine, giving relatively low I/Ca ratios for planktic and benthic foraminifera samples from poorly oxygenated waters, and high ratios for well-oxygenated waters. This suggests that both alternative methods are suitable to stabilize iodine initially dissolved in acid. Samples that contain 5–10 specimens show a wide spread in I/Ca. Samples containing 20 specimens or more show more centered I/Ca values, indicating that a larger sample size is more representative of the average planktic foraminifera community. The impact of cleaning on planktic and benthic foraminifera I/Ca ratios is very similar to Mg/Ca, with the largest effect occurring during the clay removal step. The largest iodine contaminations were recorded at locations characterized by moderate to high organic carbon contents. In those circumstances, we recommend doubling the oxidative cleaning steps (4 instead of 2 repetitions) to ensure that all organic material is removed.