Stable oxygen isotope record of epibenthic foraminifera and water samples of the Arctic Ocean

We determined d18OCib values of live (Rose Bengal stained) and dead epibenthic foraminifera Cibicidoides wuellerstorfi, Cibicides lobatulus, and Cibicides refulgens in surface sediment samples from the Arctic Ocean and the Greenland, Iceland, and Norwegian seas (Nordic Sea). This is the first time that a comprehensive d18OCib data set is generated and compiled from the Arctic Ocean. For comparison, we defined Atlantic Water (AW), upper Arctic Bottom Water (uABW), and Arctic Bottom Water (ABW) by their temperature/salinity characteristics and calculated mean equilibrium calcite d18Oequ from summer sea-water d18Ow and in situ temperatures. As a result, in the Arctic environment we compensate for Cibicidoides- and Cibicides-specific offsets from equilibrium calcite of -0.35 and -0.55 per mil, respectively. After this taxon-specific adjustment, mean d18OCib values plausibly reflect the density stratification of principle water masses in the Nordic Sea and Arctic Ocean. In addition, mean d18OCib from AW not only significantly differs from mean d18OCib from ABW, but also d18OCib from within AW differentiates in function of provenience and water mass age. Furthermore, in shallow waters brine-derived low d18Ow can significantly lower the d18OCib of Cibicides spp. and thus d18OCib may serve as a paleobrine indicator. There is no statistically significant difference, however, between deeper water masses mean d18OCib of the Nordic Sea, and of the Eurasian and Amerasian basins, and no influence of low-d18Ow brines is recorded in Recent uABW and ABW d18OCib of C. wuellerstorfi. This may be due to dilution of a low-d18Ow brine signal in the deep sea, and/or to preferential incorporation of relatively high-d18Ow brines from high-salinity shelves. Although our data encompass environments with seasonal sea-ice and brine formation supposed to ultimately ventilate the deep Arctic Ocean, d18OCib from uABW and ABW do not indicate negative excursions. This may challenge hypotheses that call for enhanced Arctic brine release to explain negative benthic d18O spikes in deep-sea sediments from the late Pleistocene North Atlantic Ocean.

Part of the global DOC versus AOU (dissolved organic carbon/apparent oxygen utilization) data compilation, Indian Ocean

Samples for total organic carbon (TOC) analysis were collected on WOCE Line P15S (0° to 67°S along 170°W) and from 53° to 67°S along 170°E in the western South Pacific, and on Line I8 (5°N to 43°S along 80°/90°E) in the central Indian Ocean. TOC concentrations in the upper ocean varied greatly between the regions studied. Highest surface TOC concentrations (81-85 µM C and 68-73 µM C) were observed in the warmest waters (>27°C) of the western South Pacific and central Indian Oceans, respectively. Lowest surface TOC concentrations (45-65 µM C) were recorded in the southernmost waters occupied (>50°S along 170°W and 170°E). Deep water (>1000 m) TOC concentrations were uniform across all regions analyzed, averaging between 42.3 and 43 µM C (SD: ±0.9 µM C). Mixing between TOC-rich surface waters and TOC-poor deep waters was indicated by the strong correlations between TOC and temperature (r2>0.80, north of 45°S) and TOC and density (r2>0.50, southernmost regions). TOC was inversely correlated with apparent oxygen utilization (AOU) along isopycnal surfaces north of the Polar Frontal Zone (PFZ) and at depths <500 m. The TOC:AOU molar ratios at densities of sigmaT 23-27 ranged from -0.15 to -0.34 in the South Pacific and from -0.13 to -0.31 in the Indian Ocean. These ratios indicate that TOC oxidation was responsible for 21%-47% and 18%-43% of oxygen consumption in the upper South Pacific and Indian Oceans, respectively. At greater depths, TOC did not contribute to the development of AOU. There was no evidence for significant export of dissolved and suspended organic carbon along isopycnal surfaces that ventilate near the PFZ.

(Table 1) Comparison of dive duration and speed of Adélie penguins (Pygoscelis adeliae) equipped with internal and external devices

Bio-logging studies suffer from the lack of real controls. However, it is still possible to compare indirect parameters between control and equipped animals to assess the level of global disturbance due to instrumentation. In addition, it is also possible to compare the behaviour of free-ranging animals between individuals equipped with different techniques or instruments to determine the less deleterious approach. We instrumented Adelie Penguins (Pygoscelis adeliae) with internal or external time-depth recorders and monitored them in parallel with a control group during the first foraging trip following instrumentation. Foraging trip duration was significantly longer in the internally-equipped group. This difference was due to a larger number of dives, reflecting a lower foraging ability or a higher food demand, and longer periods of recovery at the surface. These longer recovery periods were likely to be due to a reduced efficiency to ventilate at the surface, probably because the implanted devices pressurised adjacent organs such as air sacs. Moreover, descent and ascent rates were slightly lower in externally-equipped penguins, presumably because external instrumentation increased the bird drag. Looking at our results, implantation appears more disadvantageous - at least for short-term deployment - than external equipment in Adelie Penguins, while this method has been described to induce no negative effects in long-term studies. This underlines the need to control for potential effects due to methodological aspects in any study using data loggers in free-ranging animals, to minimise disturbance and collect reliable data.

Physical oceanography during POLARSTERN cruise ARK-XVIII/1a

In spite of the lack of bottom reaching convection in the Greenland Sea since the 1980s, convection continues to ventilate the Greenland Gyre down to intermediate depth. The variability of this ventilation activity is determined here annually for eight winters according to a multiple criteria catalogue, applied to annual summer conductivity-temperature-depth transects along 75°N. The comparison of the ventilation depths with the meteorological forcing, the ice cover, and the stratification of the water column shows the decisive influence of the hydrographic structure in the upper and intermediate layers. Ice, on the other hand, is not necessary for convection to occur. Ice formation does not even lead to particularly deep convection. A stability maximum, which currently dominates the vertical structure of the water column at medium depth, limits the ventilation depths effectively.

Benthic (C. wuellerstorfi) d18O, d13C and Cd/Ca in sediment core NEAP 4K across the last deglaciation

We present evidence that the characteristic chemical signature (based on coupled benthic foraminiferal Cd/Ca and d13C) of Antarctic Intermediate waters (AAIW) penetrated throughout the intermediate depths of the Atlantic basin to the high-latitude North Atlantic during the abrupt cooling events of the last deglaciation: Heinrich 1 and the Younger Dryas. AAIW may play the dynamic counterpart to the "bipolar seesaw" when near-freezing salty bottom waters from the Antarctic (AABW) sluggishly ventilate the deep ocean. Our data reinforce the concept that interglacial circulation is stabilized by salinity feedbacks between salty northern sourced deep waters (NADW) and fresh southern sourced waters (AABW and AAIW). Further, the glacial ocean may be susceptible to the more finely balanced relative densities of NADW and AAIW, due to either freshwater input or a reversal of the salinity gradient, such that the ocean is poised for NADW collapse via a negative salinity feedback. The unstable climate of the glacial period and its termination may arise from the closer competition for ubiquity at intermediate depths between northern and southern sourced intermediate waters.

Potential temperature in Espartel Sill (Strait of Gibraltar), from 2004-09-30 to 2016-03-02 at 344 meters depth, link to raw data in MATLAB format

Potential temperature measured with a SBE37 at 35.862ºN, 5.97ºW at 344 meters Depth. Data expand from September the 30th, 2004 to March the 2nd, 2016. Original measurement frequency was 30 minutes, the data presented here is a subsampling that extract the coldest temperature found each 12 hours. The time vector corresponds with the moment in which this minimun temperature is observed.