Species-specific consequences of ocean acidification for the calcareous tropical green algae Halimeda, 2011

Ocean acidification (OA), resulting from increasing dissolved carbon dioxide (CO2) in surface waters, is likely to affect many marine organisms, particularly those that calcify. Recent OA studies have demonstrated negative and/or differential effects of reduced pH on growth, development, calcification and physiology, but most of these have focused on taxa other than calcareous benthic macroalgae. Here we investigate the potential effects of OA on one of the most common coral reef macroalgal genera,Halimeda. Species of Halimeda produce a large proportion of the sand in the tropics and are a major contributor to framework development on reefs because of their rapid calcium carbonate production and high turnover rates. On Palmyra Atoll in the central Pacific, we conducted a manipulative bubbling experiment to investigate the potential effects of OA on growth, calcification and photophysiology of 2 species of Halimeda. Our results suggest that Halimeda is highly susceptible to reduced pH and aragonite saturation state but the magnitude of these effects is species specific. H. opuntiasuffered net dissolution and 15% reduction in photosynthetic capacity, while H. taenicola did not calcify but did not alter photophysiology in experimental treatments. The disparate responses of these species to elevated CO2 partial -pressure (pCO2) may be due to anatomical and physiological differences and could represent a shift in their relative dominance in the face of OA. The ability for a species to exert biological control over calcification and the species specific role of the carbonate skeleton may have important implications for the potential effects of OA on ecological function in the future.

Stable oxygen isotope composition of the sea water in the Mediterranean Sea

During the cruises No 17 and 22 of the German research vessel "Meteor", 45 water samples were taken at 4 stations in the central part of the Mediterranean Sea. Mass spectrometrical analyses showed that systematic, but time variable changes of the oxygen isotope ratios occur. Deep water samples (T> 500 m) have a ± constant isotopic composition of d18O = +1.79? (SMOW) and a Chlorinity of 21.399?. These data are discussed with respect to paleotemperature determinations.

Determination of Uranium, Thorium, and Ionium in sediment cores of the Caribbean and Ionian Sea

A rapid procedure for Io (Th230) dating of sediments with accumulation rates in the range of several cm/1000 years is described. Studying of large sample populations with very small Io-excess activity is possible as the counting time (around 1500 min/sample) are 2 to 5 times shorter than with the standard Io-excess method. Improved sensitivity of the Io-excess measurement is achieved by: 1) extraction ( ~90 %) of the authigenic Io-excess with EDTA, with minor leaching ( ~30 %) of the allogenic Th232 and Io-supported, 2) processing samples as large as 10 g or more. The procedure was applied to sediments from the Caribbean (V 12-122) and from the Ionian Sea (M22_48 and M17_17). In the case of the standard core V 12-122 our results are in good agreement with previous time-consuming Io determinations. The resulting average accumulation rates of 2.0 ± 0.3 cm/1000 years for the Ionian Sea cores are close to the average derived from magnetic reversal studies of a nearby core.