Cornelia Wuchter

The TEX₈₆ is a new temperature proxy which is based on the number of cyclopentane moieties in the glycerol dialkyl glycerol tetraether (GDGT) lipids of the membranes of Crenarchaeota that occur ubiquitously in oceans and shelf seas. This proxy was calibrated by core top sediments, but it is as yet not clear during which season and at which depth in the water column the GDGT signal used for TEX₈₆ paleothermometry is biosynthesized. Here we analyzed >200 particulate organic matter (POM) samples from 11 different marine settings for TEX₈₆. This revealed that the GDGTs occur seasonally in surface waters and occur in higher abundances during the winter and spring months. The depth distribution showed that GDGTs generally appeared in higher amounts below 100 m depth in the water column. However, the TEX₈₆ values for waters below the photic zone (150–1500 m) did not correlate with the in situ temperature but rather correlated linearly with surface temperature. The TEX₈₆ for POM from the upper 100 m showed a linear correlation with in situ temperature, which was nearly identical to the previously reported core top equation. The correlation of all POM samples with surface temperature was also strikingly similar to the core top correlation. These findings demonstrate that the GDGT signal which reaches the sediment is mainly derived from the upper 100 m of the water column. This may be caused by the fact that GDGTs from the photic zone are much more effectively transported to the sediment by grazing and repackaging in large particles than GDGTs from deeper waters.

Recently, a new geochemical temperature proxy, the TEX₈₆, was introduced. This proxy is based on the number of cyclopentane moieties in the glycerol dialkyl glycerol tetraethers (GDGTs) of the membrane lipids of marine Crenarchaeota, which changes as a response to temperature. However, until now, only sediment data have been used to establish this proxy, and experimental work is missing. We performed mesocosm studies with marine Crenarchaeota incubated at temperatures ranging from 5 to 35°C and salinities of 27 and 35‰ to test the validity of the TEX₈₆ proxy. Growth of marine Crenarchaeota in these mesocosms was evident from the substantial increase in the concentration of marine Crenarchaeotal membrane lipids with amounts up to 3400 ng/L. With increasing temperature, an increase in the number of cyclopentane moieties in the crenarchaeotal membrane lipids was observed. Different salinities did not show any effect on the GDGT distribution. The TEX₈₆ showed a significant linear correlation to incubation temperature: TEX₈₆ = 0.015 × T + 0.10 (r² = 0.79). This equation has a similar slope to the correlation obtained from core tops but differs in the intersection (TEX₈₆ = 0.015 × T + 0.28, r² = 0.92). This difference is mainly determined by the smaller amount of the regioisomer of crenarchaeol in the incubation series compared to core top samples. These incubation experiments indicates that water temperature is indeed the major controlling factor for the membrane distribution of marine Crenarchaeota and confirms that the TEX₈₆ proxy depends on a physiological response to regulate membrane fluidity.

Biphytanyl membrane lipids and 16S rRNA sequences derived from marine Crenarchaeota were detected in shallow North Sea surface water in February 2002. To investigate the carbon fixation mechanism of these uncultivated archaea in situ (13)C bicarbonate tracer experiments were performed with this water in the absence of light. About 70% of the detected (13)C incorporation into lipids (including fatty acids and sterols) is accounted for by the crenarchaeotal biphytanyl membrane lipids. This finding indicates that marine Crenarchaeota can utilize bicarbonate or CO(2) derived thereof in the absence of light and are chemoautotrophic organisms.