Comparison of TEX86 and UK'37 temperature proxies in sinking particles in the Cariaco Basin

The Cariaco Basin, a silled, permanently anoxic basin on the continental shelf of Venezuela with a dynamic chemocline (-240-350 m), has been subject of > 20 years of oceanographic observation and sediment trap studies. We evaluated UK'37 and the TEX86 temperature proxies using sinking particles collected in shallow sediment trap samples at 275 m (Trap A) and 455 m (Trap B) (within and below the chemocline). The organic geochemical temperature proxies, UK'37. (based on coccolithophorid alkenone lipids) and TEX86 (based on archaeal glycerol dialkyl glycerol tetraether (GDGT) lipids), use observed relationships between the ratio of specific lipids and measured sea surface temperature to hindcast past sea surface temperatures. In this study, both UK'37 and TEX86 temperature proxies record seasonal temperature variations, including the cooling associated with upwelling events. UK'37-based temperatures are colder than measured sea surface temperatures, and better correlated temperature at the chlorophyll maximum. In sediment trap material collected below the chemocline (Trap B), UK'37 values are higher than those in Trap A. Warmer subchemocline UK'37 based temperatures may be related to autooxidation of sinking particles, either by small amounts of available oxygen or by alternate electron acceptors concentrated in the biologically dynamic chemocline (e.g. intermediate sulfur compounds). The absolute flux weighted TEX86 temperature values measured in sinking particles from Trap A match the measured SST well. The differences in the TEX86 values between Traps A and B are small and reflect less impact of degradation. Overall, the TEX86 temperatures in sinking particles in the Cariaco Basin reflect annual SST.

Trace elements in the aerosol at Neumayer Station, Antarctica

Atmospheric trace element concentrations were measured from March 1999 through December 2003 at the Air Chemistry Observatory of the German Antarctic station Neumayer by inductively coupled plasma - quadrupol mass spectrometry (ICP-QMS) and ion chromatogra-phy (IC). This continuous five year long record derived from weekly aerosol sampling re-vealed a distinct seasonal summer maximum for elements linked with mineral dust entry (Al, La, Ce, Nd) and a winter maximum for the mostly sea salt derived elements Li, Na, K, Mg, Ca, and Sr. The relative seasonal amplitude was around 1.7 and 1.4 for mineral dust (La) and sea salt aerosol (Na), respectively. On average a significant deviation regarding mean ocean water composition was apparent for Li, Mg, and Sr which could hardly be explained by mir-abilite precipitation on freshly formed sea ice. In addition we observed all over the year a not clarified high variability of element ratios Li/Na, K/Na, Mg/Na, Ca/Na, and Sr/Na. We found an intriguing co-variation of Se concentrations with biogenic sulfur aerosols (methane sul-fonate and non-sea salt sulfate), indicating a dominant marine biogenic source for this element linked with the marine biogenic sulfur source.