Tab. 1: Geographical, temperature and chemical features of sites on Bear Island and Spitsbergen

In arctic populations of Macrothrix hirsuticornis life cycles are mainly governed by temperature. This was found by using laboratory cultures in combination with the analysis of population samples from waters in Svalbard. In arctic waters ex-ephippio-++ usually produce gamogenetic F1-++ together with a high percentage of oo, which have to fertilize the resting eggs. Temperatures around 14°C, which are very rare in waters of Svalbard, will induce parthenogenetic oo in the F1 and even the F2-generation, a mode of reproduction normally found in Macrothrix-populations of Central Europe. This was found in laboratory cultures of M. hirsuticornis from Bear Island, and there was evidence, that a similar cycle occurs in warm wells in Spitsbergen. The arctic distribution of M. hirsuticornis mainly depends on temperature, which regulates the speed of individual development. But this can only be understood together with the length of time, during which suitable life conditions are given. Physiological adaptations to life in waters in high latitudes could not be found, in spite of the extreme northern occurrence of M. hirsuticornis.

Occurrence of nannoplankton observed in Early Pliocene samples from Zanclean stratotype of Capo Rossello, Sicily (Table I)

Calcareous nannoplankton biostratigraphy has been worked out in the eastern Mediterranean utilizing deep-sea sediments recovered from DSDP Leg 42A Sites 375 and 376. These two drill sites were located approximately 55 km west of Cyprus on the Florence Rise. Sediments, ranging in age from early Miocene (Helicosphaera ampliaperta Zone) through Holocene, contain sufficient age-diagnostic species to recognize essentially all of the lowlatitude nannoplankton zones described by Bukry, although regional, secondary marker species are needed to define some zonal boundaries. Reworked Cretaceous and Paleogene nannoplankton occur throughout the stratigraphic interval studied, but not in quantities large enough to mask indigenous species. Sedimentation rates at Sites 375 and 376 were highest in the late Miocene and late Pleistocene. Open-marine, warm-water species of discoasters are present in significant numbers throughout the Miocene and Pliocene. Earliest Pliocene assemblages contain numerous specimens of ceratoliths. Nannoplankton in post-Messinian sediments at the drill sites and the Zanclean stratotype at Capo Rossello, Sicily, indicate that the base of the Amaurolithus tricorniculatus Zone (base of Triquetrorhabdulus rugosus Subzone) corresponds with the Miocene-Pliocene boundary.

Planktic foraminiferal abundance and faunal-derived sea surface temperature of eastern equatorial Pacific ODP Site 202-1240

Glacial cooling (~1-5°C) in the eastern equatorial Pacific (EEP) cold tongue is often attributed to increased equatorial upwelling, stronger advection from the Peru-Chile Current (PCC), and to the more remote subpolar southeastern Pacific water mass. However, evidence is scarce for identifying unambiguously which process plays a more important role in driving the large glacial cooling in the EEP. To address this question, here we adopt a faunal calibration approach using planktic foraminifers with a new compilation of coretop data from the eastern Pacific, and present new downcore variation data of fauna assemblage and estimated sea surface temperatures (SSTs) for the past 160 ka (Marine Isotope Stage (MIS) 6) from ODP Site 1240 in the EEP. With significant improvement achieved by adding more coretop data from the eastern boundary current, our downcore calibration results indicate that most of the glacial cooling episodes over the past 160 ka in the EEP are attributable to increased influence from the subpolar water mass from high latitudes of the southern Pacific. By applying this new calibration of the fauna SST transfer function to a latitudinal transect of eastern Pacific (EP) cores, we find that the subpolar water mass has been a major dynamic contributor to EEP cold tongue cooling since MIS 6.