Description: Subpolar regions are key areas to study natural climate variability, due to their high sensitivity to rapid environmental changes, particularly through sea surface temperature (SST) variations. Here, we have tested three independent organic temperature proxies (UK'37, TEX86 and LDI) on their potential applicability for SST reconstruction in the subpolar region around Iceland. UK'37, TEX86 and TEXL86 temperature estimates from suspended particulate matter showed a substantial discrepancy with instrumental data, while long chain alkyl diols were below detection limit in most of the stations. In the northern Iceland Basin, sedimenting particles revealed a seasonality in lipid fluxes i.e. high fluxes of alkenones and GDGTs were measured during late spring-summer, and high fluxes of long chain alkyl diols during late summer. The flux-weighted average temperature estimates had a significant negative (ca. 2.3°C for UK'37) and positive (up to 5°C for TEX86) offset with satellite-derived SSTs and temperature estimates derived from the underlying surface sediment. UK'37 temperature estimates from surface sediments around Iceland correlate well with summer mean sea surface temperatures, while TEX86 derived temperatures correspond with both annual and winter mean 0-200 m temperatures, suggesting a subsurface temperature signal. Anomalous LDI-SST values in surface sediments, and low mass flux of 1,13- and 1,15-diols compared to 1,14-diols, suggest that Proboscia diatoms are the major sources of long chain alkyl diols in this area rather than eustigmatophyte algae, and therefore the LDI cannot be applied in this region.

Description: Oxygen exposure has a large impact on lipid biomarker preservation in surface sediments and may affect the application of organic proxies used for reconstructing past environmental conditions. To determine its effect on long chain alkyl diol and keto-ol based proxies, the distributions of these lipids was studied in nine surface sediments from the Murray Ridge in the Arabian Sea obtained from varying water depths (900 to 3000 m) but in close lateral proximity and, therefore, likely receiving a similar particle flux. Due to substantial differences in bottom water oxygen concentration (〈3 to 77 µmol/L) and sedimentation rate, substantial differences exist in the time the biomarker lipids are exposed to oxygen in the sediment. Long chain alkyl diol and keto-ol concentrations in the surface sediments (0-0.5 cm) decreased progressively with increasing oxygen exposure time, suggesting increased oxic degradation. The 1,15-keto-ol/diol ratio (DOXI) increased slightly with oxygen exposure time as diols had apparently slightly higher degradation rates than keto-ols. The ratio of 1,14- vs. 1,13- or 1,15-diols, used as upwelling proxies, did not show substantial changes. However, the C30 1,15-diol exhibited a slightly higher degradation rate than C28 and C30 1,13-diols, and thus the Long chain Diol Index (LDI), used as sea surface temperature proxy, showed a negative correlation with the maximum residence time in the oxic zone of the sediment, resulting in ca. 2-3.5 °C change, when translated to temperature. The UK'37 index did not show significant changes with increasing oxygen exposure. This suggests that oxic degradation may affect temperature reconstructions using the LDI in oxic settings and where oxygen concentrations have varied substantially over time.

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.