This paper discusses the faunal content, the mammal biostratigraphy, and the environmental ecology of three important continental Tertiary vertebrate faunas from the Lower Rhine Embayment. The sites investigated are Rott (MP 30, Late Oligocene), Hambach 6C (MN 5, Middle Miocene), Frechen and Hambach 11 (both MN 16, Late Pliocene). Comparative analysis of the entire faunas shows the assemblages to exhibit many conformities in their general composition, presumably resulting from their preference for wet lowlands. It appears that very similar environmental conditions for vertebrates reoccurred during at least 20 Ma although the sites are located in a tectonically active region with high subsidence rates. Differences in the faunal composition are partly due to local differences in the depositional environment of the sites: lake deposits at the margin of the embayment (Rott), coal swamp and estuarine conditions in the centre of the embayment (Hambach 6C), and flood plain environments with small rivulets (Frechen and Hambach 11). The composition of the faunal assemblages (diversity and taxonomy) also documents faunal turnovers with extinctions and immigrations (Oligocene/Miocene and postMiddle Miocene), as a result of changing climate conditions.

Additional vertebrate faunal data were retrieved from two new assemblages collected from younger strata at the Hambach mine (Hambach 11C and 14). They are important for the understanding of the Plio-Pleistocene transition in the southern part of the Lower Rhine Embayment and for correlating depositional sequences in the Dutch/German borderland.

Psephophorus polygonus Meyer, 1847, the first fossil leatherback turtle to be named, was described on the basis of shell ossicles from the middle Miocene (MN6–7/8?) of Slovakia. The whereabouts of this material is uncertain but a slab on display at the Naturhistorisches Museum Wien is considered the neotype. We rediscovered further type locality ossicles in four European institutions, re-evaluated their gross morphology and described for the first time their microstructure by comparing them with Dermochelys coriacea, the only living dermochelyid turtle. The gross morphology is congruent with that already described for P. polygonus, but with two significant exceptions: the ridged ossicles of P. polygonus may have a distinctly concave ventral surface as well as a tectiform shape in cross-section. They do not develop the external keel typical of many ossicles of D. coriacea. Both ridged and non-ridged ossicles of P. polygonus are characterized by compact diploe structures with an internal cortex consisting of a coarse fibrous meshwork, whereas the proportionately thinner ossicles of D. coriacea tend to lose the internal cortex, and thus their diploe, during ontogeny. The ossicles of both P. polygonus and D. coriacea differ from those of other lineages of amniotes whose carapace is composed of polygonal ossicles or platelets, in having growth centres situated at the plate centres just interior to the external bone surface and not within the cancellous core or closer to the internal compact layer. The new diagnosis of P. polygonus allows us to preliminarily re-evaluate the taxonomy of some of the Psephophorus-like species. Despite some macro- and micromorphological differences, it seems likely that Psephophorus was as cosmopolitan as extant Dermochelys and had a broadly similar ecology, with a possible difference concerning the dive depth.

Palaeoenvironmental changes in the upper Middle Miocene Central Paratethys were reconstructed by using qualitative and quantitative palaeontological analyses of foraminifera and ostracods, coupled with trace elemental (Mg/Ca) and stable isotope (δ18O and δ13C) analyses of their carbonate skeletons and of gastropod shells. Mean annual air temperatures were estimated using the oxygen isotope composition of contemporaneous rodent teeth. The studied aquatic fossils come from two boreholes in the Zsámbék Basin (northern central Hungary), while the terrestrial ones are from localities in NE Hungary and E Romania. In the studied Sarmatian successions, three zones could be distinguished, based on palaeontological and geochemical results. At the Badenian/Sarmatian boundary, faunal diversity decreased markedly. In the lower zone a transgressive event culminated in a seawater incursion into the semi-open basin system of the Central Paratethys. Stable bottom-water temperature (~15 °C) and variable salinities (20–32 ‰) are estimated for the Early Sarmatian Sea. The faunal changes (notably a strong reduction in biodiversity) occurring at the boundary between the lower and the middle zone can be explained by a sea-level highstand with dysoxic conditions. A relative sea-level fall is documented at the end of this middle zone. After a short regressive event, a marine connection between the Paratethys and the Mediterranean was established at the beginning of the upper zone. This is indicated by an increased microfaunal diversity and the re-appearance of marine Badenian ostracods and foraminifera, which are completely absent from the older Sarmatian series. During the upper zone, the temperatures and salinities are estimated to have fluctuated from 15 °C to 21 °C and from 15 ‰ to 43 ‰, respectively.

Southern Ocean palaeocirculation is clearly related to the formation of a continental ice sheet on Antarctica and the opening of gateways between Antarctica and the Australian and South American continents. Palaeoenvironmental proxy records from Southern Ocean sediment cores suggest ice growth on Antarctica beginning by at least 40 million years (Ma) ago, and the opening of Tasmania–Antarctic and Drake Passages to deep-water flow around 34 and 31 ± 2 Ma, respectively. So, the Eocene/Oligocene transition appears to mark the initiation of the Antarctic Circumpolar Current and thus the onset of thermal isolation of Antarctica with a first major ice volume growth on East Antarctic. There is no evidence for a significant cooling of the deep ocean associated with this rapid (< 350 000 years) continental ice build-up. After a long phase with frequent ice sheets growing and decaying, in the middle Miocene at about 14 Ma, a re-establishment of an ice sheet on East Antarctica and the Pacific margin of West Antarctica was associated with an increased southern bottom water formation, and a slight cooling of the deep ocean, but with no permanent drop in atmospheric pCO2. During the late Pleistocene on orbital time scales a temporal correlation between changes in atmospheric pCO2 and proxy records of deep ocean temperatures, continental ice volume, sea ice extension, and deep-water nutrient contents is documented. I discuss hypotheses that call for a dominant control of glacial to interglacial atmospheric pCO2 variations by Southern Ocean circulation dynamics. Millennial to centennial climate variability is a global feature, but there is contrasting evidence from various palaeoclimate archives that indicate both interhemispheric synchrony and asynchrony. The role of the Southern Ocean, however, in triggering or modulating climate variability on these time scales only recently received some attention and is not yet adequately investigated.