Age determination and paleotemperatures of sediment core MD95-2043 in the Alboran Sea

Past sea surface temperature (SST) evolution in the Alboran Sea (western Mediterranean) during the last 50,000 years has been inferred from the study of C37 alkenones in International Marine Global Change Studies MD952043 core. This record has a time resolution of ~200 years allowing the study of millennial-scale and even shorter climatic changes. The observed SST curve displays characteristic sequences of extremely rapid warming and cooling events along the glacial period. Comparison of this Alboran record with delta18O from Greenland ice (Greenland Ice Sheet Project 2 core) shows a strong parallelism between these SST oscillations and the Dansgaard-Oeschger events. Five prominent cooling episodes standing out in the SST profile are accompanied by an anomalous high abundance of Neogloboquadrina pachyderma sinistral which is confined to the duration of these cold intervals. These features and the isotopic record reflect drastic changes in the surface hydrography of the Alboran Sea in association with Heinrich events Hl-5.

(Table 1) Primary production in the Arabian Sea in May-July 1966

A radiocarbon survey of primary production in the Arabian Sea was carried out during May to July 1966. Production ranged from 0.8 to 30 mg C/m**3 per day at the surface, and from 0.1 to 3 g C/m**2 per day in the photosynthetic layer. At most stations photosynthesis was found to be maximum at depths of 25-30 m, and its lower limit was at 75 m.

Contemporary genetic, historical genetic and morphological data sets for the Yellow-tufted Honeyeater Lichenostomus melanops

Understanding the evolutionary history of threatened populations can improve their conservation management. Re-establishment of past but recent gene flow could re-invigorate threatened populations and replenish genetic diversity, necessary for population persistence. One of the four nominal subspecies of the common yellow-tufted honeyeater, Lichenostomus melanops cassidix, is critically endangered despite substantial conservation efforts over 55 years. Using a combination of morphometric, genetic and modelling approaches we tested for its evolutionary distinctiveness and conservation merit. We confirmed that cassidix has at least one morphometric distinction. It also differs genetically from the other subspecies in allele frequencies but not phylogenetically, implying that its evolution was recent. Modelling historical distribution supported the lack of vicariance and suggested a possibility of gene flow among subspecies at least since the late Pleistocene. Multi-locus coalescent analyses indicated that cassidix diverged from its common ancestor with neighbouring subspecies gippslandicus sometime from the mid-Pleistocene to the Holocene, and that it has the smallest historical effective population size of all subspecies. It appears that cassidix diverged from its ancestor with gippslandicus through a combination of drift and local selection. From patterns of genetic subdivision on two spatial scales and morphological variation we concluded that cassidix, gippslandicus and (melanops + meltoni) are diagnosable as subspecies. Low genetic diversity and effective population size of cassidix may translate to low genetic fitness and evolutionary potential, thus managed gene flow from gippslandicus is recommended for its recovery.