ALBERT

Description: Two high-resolution sediment cores from eastern Fram Strait have been investigated for sea subsurface and surface temperature variability during the Holocene (the past ca 12,000 years). The transfer function developed by Husum and Hald (2012) has been applied to sediment cores in order to reconstruct fluctuations of sea subsurface temperatures throughout the period. Additional biomarker and foraminiferal proxy data are used to elucidate variability between surface and subsurface water mass conditions, and to conclude on the Holocene climate and oceanographic variability on the West Spitsbergen continental margin. Results consistently reveal warm sea surface to subsurface temperatures of up to 6 °C until ca 5 cal ka BP, with maximum seawater temperatures around 10 cal ka BP, likely related to maximum July insolation occurring at that time. Maximum Atlantic Water (AW) advection occurred at surface and subsurface between 10.6 and 8.5 cal ka BP based on both foraminiferal and dinocyst temperature reconstructions. Probably, a less-stratified, ice-free, nutrient-rich surface ocean with strong AW advection prevailed in the eastern Fram Strait between 10 and 9 cal ka BP. Weakened AW contribution is found after ca 5 cal ka BP when subsurface temperatures strongly decrease with minimum values between ca 4 and 3 cal ka BP. Cold late Holocene conditions are furthermore supported by high planktic foraminifer shell fragmentation and high d18O values of the subpolar planktic foraminifer species Turborotalita quinqueloba. While IP25-associated indices as well as dinocyst data suggest a sustained cooling due to a decrease in early summer insolation and consequently sea-ice increase since about 7 cal ka BP in surface waters, planktic foraminiferal data including stable isotopes indicate a slight return of stronger subsurface AW influx since ca 3 cal ka BP. The observed decoupling of surface and subsurface waters during the later Holocene is most likely attributed to a strong pycnocline layer separating cold sea-ice fed surface waters from enhanced subsurface AW advection. This may be related to changes in North Atlantic subpolar versus subtropical gyre activity.

Description: The mode and vigor of the global oceanic circulation critically depend on the salinity of (sub)surface water masses advected to the loci of deep-water formation. Within the Atlantic meridional overturning circulation (AMOC), an important supplier of high-salinity waters is the Mediterranean Outflow Water (MOW), discharging into the North Atlantic via the Strait of Gibraltar. Despite its importance for the North Atlantic salinity budget, the long-term dynamics of MOW production have remained poorly understood. Here we present high-resolution records of bottom-current velocity from three drill sites within the Gulf of Cádiz that document a persistent low-latitude forcing of MOW flow speed over the past ~150 k.y. We demonstrate that the African monsoon is the predominant driver of orbital-scale MOW variability via its influence on the freshwater budget of the eastern Mediterranean Sea. Consequently, MOW formation fluctuates in concert with orbital precession overprinted by centennial-scale oscillations of high-latitude origin. We further document that Northern Hemisphere summer insolation minima stimulate maximal injection of MOW-derived salt into the North Atlantic, likely strengthening the intermediate AMOC branch. The direct coupling of MOW dynamics to low-latitude climate forcing represents a hitherto neglected process for propagating (sub)tropical climate signals into the high northern latitudes.

Description: In a sediment core from the Pacific sector of the Antarctic Zone (AZ) of the Southern Ocean, we report diatom-bound N isotope (d15Ndb) records for total recoverable diatoms and two distinct diatom assemblages (pennate and centric rich). These data indicate tight coupling between the degree of nitrate consumption and Antarctic climate across the last two glacial cycles, with d15Ndb (and thus the degree of nitrate consumption) increasing at each major Antarctic cooling event. Coupled with evidence from opal- and barium-based proxies for reduced export production during ice ages, the d15Ndb increases point to ice age reductions in the supply of deep ocean-sourced nitrate to the AZ surface. The two diatom assemblages and species abundance data indicate that the d15Ndb changes are not the result of changing species composition. The pennate and centric assemblage d15Ndb records indicate similar changes but with a significant decline in their difference during peak ice ages. A tentative seasonality-based interpretation of the centric-to-pennate d15Ndb difference suggests that late summer surface waters became nitrate free during the peak glacials.

Description: The TEX86H paleothermometer based on isoprenoid glycerol dialkyl glycerol tetraethers (isoGDGTs) has widely been applied in various marine settings to reconstruct past sea surface temperatures (SSTs). However, it still remains uncertain how well this proxy reconstructs annual mean SSTs. Here, we assess environmental factors governing the TEX86H paleothermometer in the Mediterranean Sea, by studying the distribution of isoGDGTs in surface sediments, suspended particulate matter (SPM), and two sediment cores. A redundancy analysis using the fractional abundance of the six major isoGDGTs indicates that the sedimentary isoGDGTs are mostly influenced by three environmental factors explaining a large part (74%) of the variance in isoGDGT distribution. In order of decreasing significance, these factors are annual mean SST, continental organic matter input as indicated by the BIT index, and water depth. However, when considering only the four isoGDGTs that are used for the TEX86H proxy, water depth is the most significant parameter, explaining 63% of the variance. Indeed, a strong positive relationship between water depth and TEX86H is observed in both surface sediments and SPM from the Mediterranean Sea. This is driven by an increase in fractional abundances of GDGT-2 and crenarchaeol regio-isomer and a decrease in the fractional abundances of GDGT-1 and GDGT-3 with increasing water depth, leading to a bias to higher temperatures of TEX86H in deep-water surface sediments. The fact that the water-depth trend is also apparent in SPM suggests that this change might be due to a change in thaumarchaeotal community thriving below surface mixed-layer waters and that this signal is, at least partly, incorporated into sedimentary isoGDGTs. Interestingly, surface-sediment TEX86H values from 〉1000 m water depth do not show a correlation with water depth anymore and instead are correlated to annual mean SSTs. A composite deep-water TEX86H dataset of surface sediments from both the Mediterranean Sea and the Red Sea, interconnected regional restricted basins with relatively high bottom-water temperatures and high salinity, forms a distinctive correlation line, statistically distinct from that of the general global correlation. Application of this correlation on two sedimentary records from the western Mediterranean Sea covering the last deglaciation yields SSTs nearly identical to those obtained with the UK'37 paleothermometer, whereas the global calibration substantially overestimates SSTs. Our results show that the warm bias of the TEX86H proxy in the Mediterranean Sea is not due to seasonality, as previously suggested. Further research is needed to elucidate the mechanism behind the strong water depth trend of TEX86H in the Mediterranean Sea which is not apparent in open ocean settings.

Description: The aim of the present study was to evaluate the influence of different light quality, especially ultraviolet radiation (UVR), on the dynamics of volatile halogenated organic compounds (VHOCs) at the sea surface. Short term experiments were conducted with floating gas-tight mesocosms of different optical qualities. Six halocarbons (CH3I, CHCl3, CH2Br2, CH2ClI, CHBr3 and CH2I2), known to be produced by phytoplankton, together with a variety of biological and environmental variables were measured in the coastal southern Baltic Sea and in the Raunefjord (North Sea). These experiments showed that ambient levels of UVR have no significant influence on VHOC dynamics in the natural systems. We attribute it to the low radiation doses that phytoplankton cells receive in a normal turbulent surface mixed layer. The VHOC concentrations were influenced by their production and removal processes, but they were not correlated with biological or environmental parameters investigated. Diatoms were most likely the dominant biogenic source of VHOCs in the Baltic Sea experiment, whereas in the Raunefjord experiment macroalgae probably contributed strongly to the production of VHOCs. The variable stable carbon isotope signatures (d13C values) of bromoform (CHBr3) also indicate that different autotrophic organisms were responsible for CHBr3 production in the two coastal environments. In the Raunefjord, despite strong daily variations in CHBr3 concentration, the carbon isotopic ratio was fairly stable with a mean value of -26 per mil. During the declining spring phytoplankton bloom in the Baltic Sea, the d13C values of CHBr3 were enriched in 13C and showed noticeable diurnal changes (-12 per mil ± 4). These results show that isotope signature analysis is a useful tool to study both the origin and dynamics of VHOCs in natural systems.

Description: This study examined recent coccolith surface sediment assemblages across the Pacific sector of the Southern Ocean (from Punta Arenas, Chile toWellington, New Zealand). Twenty five stations located within 44.4°S to 65.4°S and 80.1°W to 174.5°E were selected in order to assess if and how the surface sediment assemblages reflect the present-day coccolithophore community and surface-water oceanographic conditions. The highest numbers of coccoliths in the surface sediments are reached near the East Pacific Rise and close to the Subtropical Front, at the New Zealand Margin (〉6x109 coccoliths/g of sediment). The dominant taxa are Emiliania huxleyi (including types A, B, B/C and C), Calcidiscus leptoporus, Gephyrocapsa spp. (including G. muellerae, G. oceanica and G. ericsonii), Umbellosphaera tenuis and Coccolithus braarudii. Despite the recognition of species morphotypes being hampered by carbonate dissolution at some locations, we observed that numbers generally decrease southward until almost a monospecific and sporadic record of E. huxleyi (types B/C and C) and C. leptoporus south of the Polar Front occurs. The recent coccolithophore distribution was compared to already published living coccolithophore distributions (i.e., water column samples collected at the same specific locations) showing a fairly similar pattern. Combining the numbers of cells/l and coccoliths/g of sediment, different coccolithophore assemblages were established coincidentwith areas bounded by the major surface oceanographic fronts, i.e. the Subantarctic Zone and the Polar Front Zone.

Description: Oceanic dissolved organic carbon (DOC) is an important carbon pool, similar in magnitude to atmospheric CO2, but the fate of its oldest forms is not well understood (Dittmar and Stubbins, 2014; Hansell, 2013, doi:10.1146/annurev-marine-120710-100757). Hot hydrothermal circulation may facilitate the degradation of otherwise un-reactive dissolved organic matter, playing an important role in the long-term global carbon cycle. The oldest, most recalcitrant forms of DOC, which make up most of oceanic DOC, can be recovered by solid-phase extraction. Here we present measurements of solid-phase extractable DOC from samples collected between 2009 and 2013 at seven vent sites in the Atlantic, Pacific and Southern oceans, along with magnesium concentrations, a conservative tracer of water circulation through hydrothermal systems. We find that magnesium and solid-phase extractable DOC concentrations are correlated, suggesting that solid-phase extractable DOC is almost entirely lost from solution through mineralization or deposition during circulation through hydrothermal vents with fluid temperatures of 212-401 °C. In laboratory experiments, where we heated samples to 380 °C for four days, we found a similar removal efficiency. We conclude that thermal degradation alone can account for the loss of solid-phase extractable DOC in natural hydrothermal systems, and that its maximum lifetime is constrained by the timescale of hydrothermal cycling, at about 40 million years (Elderfield and Schultz, 1996, doi:10.1146/annurev.earth.24.1.191).