Description: Seasonal variations in fluxes of isoprenoid glycerol dialkyl glycerol tetraethers (GDGTs) and the estimated temperatures based on TEX86 are examined in sinking particles collected using moored sediment traps in the eastern Atlantic upwelling regions. In the equatorial Guinea Basin, GDGT fluxes show a correlation with opal fluxes, implying that GDGTs are mainly transported via aggregation with diatoms. The flux-weighted TEXH86 temperatures derived from particles collected both at 853 m and 3,921 m depth correspond to the water temperature (24.1 °C) of ca. 50 m depth, where nitrate concentration starts to increase, potentially as a consequence of nitrification by Thaumarchaeota. This suggests that nutrient concentrations may affect the depth habitat of Thaumarchaeota, and it determines at which water depth the TEXH86 temperature is recorded. In the coastal upwelling off Namibia, TEXH86 temperatures are similar to satellite-derived sea surface temperature (SST) during the warm season, but the record derived from the trap is delayed relative to the SST by approximately 26 days. Warm biases, however, occur during the cold season, similar to what has previously been observed in the filamentous upwelling region off Cape Blanc. In both coastal upwelling regions, oxygen minimum zones (OMZs) are a common feature, and higher TEX86 values have been found within the OMZs in the water column off Cape Blanc and elsewhere. Thus, contributions from GDGTs produced in OMZs might explain the warmer temperature estimates during the cold season in both regions. We thus conclude that in the eastern Atlantic upwelling system, TEXH86 temperature estimates are influenced by non-thermal factors such as nutrient depth distributions and GDGTs produced in the OMZ. In paleoenvironmental records of TEX86, non-thermal signals have to be considered on regional scales.

Description: The temporal succession of changes in Amazonian hydroclimate during Heinrich Stadial 1 (HS1) (ca. 18-14.7 cal ka BP) is currently poorly resolved. Here we present HS1 records based on isotope, inorganic and organic geochemistry from a marine sediment core influenced by the Amazon River discharge. Our records offer a detailed reconstruction of the changes in Amazonian hydroclimate during HS1, integrated over the basin. We reconstructed surface water hydrography using stable oxygen isotopes (d18O) and Mg/Ca-derived paleotemperatures from the planktonic foraminifera Globigerinoides ruber, as well as salinity changes based on stable hydrogen isotope (dD) of palmitic acid. We also analyzed branched and isoprenoid tetraether concentrations, and compared them to existing bulk sediment ln(Fe/Ca) data and vegetation reconstruction based on stable carbon isotopes from n-alkanes, in order to understand the relationship between continental precipitation, vegetation and sediment production. Our results indicate a two-phased HS1 (HS1a and HS1b). During HS1a (18-16.9 cal ka BP), a first sudden increase of sea surface temperatures (SST) in the western equatorial Atlantic correlated with the slowdown of the Atlantic Meridional Overturning Circulation (AMOC) and the associated southern hemisphere warming phase of the bipolar seesaw. This phase was also characterized by an increased delivery of terrestrial material. During HS1b (16.9-14.8 cal ka BP), a decrease in terrestrial input was, however, associated with a marked decline of seawater d18O and palmitic acid dD. Both isotopic proxies independently indicate a drop in sea surface salinity (SSS). A number of records under the influence of the North Brazil Current, in contrast, indicate increases in SST and SSS resulting from a weakened AMOC during HS1. Our records thus suggest that the expected increase in SSS due to the AMOC slowdown was overridden by a two-phased positive precipitation anomaly in Amazonian hydroclimate.

Description: The western tropical Atlantic plays an important role in the interhemispheric redistribution of heat during millennial-scale changes in the strength of the Atlantic Meridional Overturning Circulation (AMOC). The proper evaluation of this role depends on a clear understanding of sea surface temperature (SST) variations during AMOC slowdown periods like Heinrich Stadials (HS) in the western tropical Atlantic. However, published SST records from the western tropical Atlantic between ca. 4°S and 7°N show inconsistencies that are apparently related to the employed temperature proxy (i.e., Mg/Ca versus alkenone unsaturation index U37k′). In general, while Mg/Ca values indicate warming during Heinrich Stadials, U37k′ values show cooling. To assess this issue, we sampled core GeoB16224-1 retrieved off French Guiana (i.e., 6°39.38′N) and reconstructed water temperatures at high resolution using Mg/Ca on the foraminifera species Globigerinoides ruber, U37k′, TEX86 and modern analogue technique (MAT) transfer functions using planktonic foraminifera assemblages calibrated for 50 m water depth. Our results show that Mg/Ca and TEX86 values recorded an increase in SST related to AMOC slowdown. Conversely, U37k′ and MAT values registered a decrease in temperatures during HS3 and HS1. Our U37k′ and Mg/Ca results thus confirm the previously reported inconsistency for the period between 48-13 cal ka BP. We suggest that several non-thermal physiological effects probably imparted a negative temperature bias on the U37k′ temperatures during Heinrich Stadials. However, MAT-based temperatures show similar variability with U37k′-based temperatures. Hence, we also suggest that during severe slowdown periods of the AMOC, a steeper meridional temperature gradient together with a southward shift of the Intertropical Convergent Zone produced not only an increase in SST but also a stronger upper water column stratification and a shoaling of the thermocline, decreasing subsurface temperatures. Our new high resolution temperature records allow a better characterization of the thermal response of the upper water column in the tropical western Atlantic to slowdown events of the AMOC, reconciling previously discrepant records.

Description: This is the temperature lipid proxy (GDGT) data measured in sinking particles collected using a sediment trap mooring system in the eastern Fram Strait and in the Antarctic Polar Front of the Atlantic sector. In the eastern Fram Strait (FEVI16), particles were collected at 1296 m water depth. In the Antarctic Polar Front (PF3), particles were collected at 614 m and 3196 m water depth. Using this dataset, TEX86-derived temperatures and OH-GDGTs-derived temperatures can be calculated.

Description: Compound-specific radiocarbon dating often requires working with small samples of 〈 100 µg carbon (µgC). This makes the radiocarbon dates of biomarker compounds very sensitive to biases caused by extraneous carbon of unknown composition, a procedural blank, which is introduced to the samples during the steps necessary to prepare a sample for radiocarbon analysis by accelerator mass spectrometry (i.e., isolating single compounds from a heterogeneous mixture, combustion, gas purification and graphitization). Reporting accurate radiocarbon dates thus requires a correction for the procedural blank. We present our approach to assess the fraction modern carbon (F14C) and the mass of the procedural blanks introduced during the preparation procedures of lipid biomarkers (i.e. n-alkanoic acids) and lignin phenols. We isolated differently sized aliquots (6-151 µgC) of n-alkanoic acids and lignin phenols obtained from standard materials with known F14C values. Each compound class was extracted from two standard materials (one fossil, one modern) and purified using the same procedures as for natural samples of unknown F14C. There was an inverse linear relationship between the measured F14C values of the processed aliquots and their mass, which suggests constant contamination during processing of individual samples. We used Bayesian methods to fit linear regression lines between F14C and 1/mass for the fossil and modern standards. The intersection points of these lines were used to infer F14Cblank and mblank and their associated uncertainties. We estimated 4.88±0.69 μgC of procedural blank with F14C of 0.714±0.077 for n-alkanoic acids, and 0.90±0.23 μgC of procedural blank with F14C of 0.813±0.155 for lignin phenols. These F14Cblank and mblank can be used to correct AMS results of lipid and lignin samples by isotopic mass balance. This method may serve as a standardized procedure for blank assessment in small-scale radiocarbon analysis.