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Marine Isotope Stage 3 (MIS 3, ca. 60–30 ka) is characterized by dynamic alternations of forest expansion with semi-arid area expansion in accordance with the warming and cooling, respectively, of the sea-surface temperatures in Northern Europe. It was in this context of rapid fluctuations that the terrestrial sequence of Caverne Marie-Jeanne (Hastière-Lavaux, Belgium) in northwestern Europe was formed. The habitat weighting method and the bioclimaticmodel, as well as the Simpson diversity index, are applied to the small-mammal assemblage of CaverneMarie-Jeanne in order to reconstruct the environmental and climatic fluctuations that are reflected in the MIS 3 sequence of the cave. Revision of the small-mammal fossil material deposited in the collections of the Royal Belgian Institute of Natural Sciences (RBINS, Brussels, Belgium) shows that the lower layers (6 to 4) of the cave, pertaining to MIS 3 (ca. 50–40 ka), underwent cold, dry environmental and climatic conditions for these layers. This is indicated by temperatures lower than at present and precipitation slightly higher than at present, together with an environment dominated by openwoodland formations and open dry meadows. Our results are consistent with the available chronological, large-mammal, herpetofaunal and mollusc datasets for this lower part of the sequence. They are also consistentwith regional loess studies in Belgium andwith previouswork performed on small mammals from MIS 3 in Belgium and elsewhere in Europe.

The environmental and climatic conditions of the Late Pleistocene of Southern Belgium are here determined for the final part of Marine Isotope Stage 3 (MIS 3) and for MIS 2 on the basis of a study of rodent assemblages. This paper provides a synthesis of several sets of environmental and climatic data from Late Pleistocene sites, all of which are located in southern Belgium. One has previously been published (Caverne Marie-Jeanne), and seven are unpublished (Cavernes de Goyet, Trou des Nutons, Trou du Frontal, Trou de Chaleux, Grotte la Chefalize, Trou du Chˆene, and Trou du Sureau). The habitat weighting and quantified ecology methods are applied to rodent material housed in the Royal Belgian Institute of Natural Sciences (RBINS, Brussels), and previous radiocarbon dates are updated, in order to reconstruct past environments. Among all the sites under analysis, the quantified ecology method shows that Trou de Chaleux corresponds to the coldest temperatures and lowest precipitation. Trou de Chaleux, with a chronology between ca. 15,964–14,014 cal yr B.P., could probably be placed in Greenland Stadial 2 (GS2) or Heinrich Event 1 (HE1). It has a rodent assemblage associated with a predominance of open dry and rocky formations, the most abundant species being the collared lemming and the narrow-headed vole. These data are found to coincide with previous studies carried out on the large-mammal, herpetofaunal, and avifaunal associations of the site, as well as on small-mammal associations from other sites in southern Belgium with similar chronology, such as Grotte Walou. Taken together, this indicates that these latest Pleistocene intervals in southern Belgium were characterized by harsh climatic and environmental conditions. In contrast, the other assemblages under study yielded much more heterogeneous results, frequently inconsistent with an attribution to the Pleistocene. This is likely to be a result of their admixture with Holocene material due to recent intrusions.

Leatherbacks constitute a bizarre clade of marine turtles today represented by a single species, Dermochelys coriacea. A series of peculiar physiological adaptations and behaviors make this species particularly reminiscent to some marine mammals. These include particularly advanced skeleton adaptations for swimming, the largest body size among living reptiles, highly elevated growth and metabolic rates, and coldwater tolerance, which enable D. coriacea to lead a truly pelagic, highly migratory, cosmopolitan lifestyle. It is one of the deepest diving animal today, which aids searching for its almost exclusive prey of jellyfishes. Due to their pelagic lifestyle and reduced skeleton, however, the fossil record of leatherbacks is very poor. Here we evaluate the skeletal anatomy of Eosphargis gigas from the Ypresian of Belgium, represented by one of the earliest and most completely preserved fossil dermochelyid. E. gigas already shows several of the anatomical specializations of the extant leatherback but it is primitive in retaining a more ossified shell. The autapomorphic rugose surface decoration of the dermal skull indicates high degree of vascularization, which in turn likely aided regulation of acid–base balance relating to hypercapnia (excess blood carbon dioxide) and/or lactate acidosis based on modern and fossil analogies. Both type of acidosis typically occurs during diving and thus E. gigas likely had deep diving capabilities, which is consistent with its postcranial skeleton. The jaw apparatus also shares many specializations with D. coriacea that may represent adaptation for preying on jellyfish. The emerging hypothesis is that the skeletal and physiological adaptations of leatherbacks are all related to feeding specializations and associated deep diving. Many of these evolved early in the lineage under greenhouse climatic conditions with the likely associated deeper placement of the gelatinous plankton zone compared to icehouse conditions. This study was supported by the SYNTHESYS program (grants AT-TAF 1441, FR-TAF 4290, GB-TAF 1882, BE-TAF 5292); Train2Move-Marie Curie Fellowship awarded to M.R.

The Late Eocene and Early Oligocene sedimentary succession in the Fayum, Egypt records the progressive development of northerly flowing Nile-type African drainage. New biostratigraphic dating of these units allows the calibration of the paleomagnetic record, the combination of dating methods enabling a detailed chronology of events to be studied. Between about 38 and 35 Ma there was a dramatic change in sedimentary regime and vast quantities of clasticmaterial were transported into the area, smothering the underlying carbonate platform and initiating a stepwise progradation of clastic units. The sudden change in sediment availability coincideswith the beginning of uplift and volcanic activity in the Turkana region of East Africa, cutting off preexisting easterly drainage from the middle of the continent. The Fayum succession therefore records the initiation of northerly drainage of central and eastern Africa, and the origins of themodern Nile watershed. The development of the current route of the Nile, with the incision of the current Nile Valley, was slightly later and related tomid Oligocene uplift of the Red Sea margins and Messinian base level fall.

Talk presented by Jiri Frank on 09/09/2012 in session 10: Nautilids of the 9th ISCPP in Zurich, Switzerland

The present monograph includes general systematic considerations on the family Epimeriidae, a revision of the genus Epimeria Costa in Hope, 1851 in the Southern Ocean, and a shorter account on putatively related eusiroid taxa occurring in Antarctic and sub-Antarctic seas. The former epimeriid genera Actinacanthus Stebbing, 1888 and Paramphithoe Bruzelius, 1859 are transferred to other families, respectively to the Acanthonotozomellidae Coleman & J.L. Barnard, 1991 and the herein re-established Paramphithoidae G.O. Sars, 1883, so that only Epimeria and Uschakoviella Gurjanova, 1955 are retained within the Epimeriidae Boeck, 1871. The genera Apherusa Walker, 1891 and Halirages Boeck, 1891, which are phylogenetically close to Paramphithoe, are also transferred to the Paramphithoidae. The validity of the suborder Senticaudata Lowry & Myers, 2013, which conflicts with traditional and recent concepts of Eusiroidea Stebbing, 1888, is questioned. Eight subgenera are recognized for Antarctic and sub-Antarctic species of the genus Epimeria: Drakepimeria subgen. nov., Epimeriella K.H. Barnard, 1930, Hoplepimeria subgen. nov., Laevepimeria subgen. nov., Metepimeria Schellenberg, 1931, Pseudepimeria Chevreux, 1912, Subepimeria Bellan-Santini, 1972 and Urepimeria subgen. nov. The type subgenus Epimeria, as currently defined, does not occur in the Southern Ocean. Drakepimeria species are superficially similar to the type species of the genus Epimeria: E. cornigera (Fabricius, 1779), but they are phylogenetically unrelated and substantial morphological differences are obvious at a finer level. Twenty-seven new Antarctic Epimeria species are described herein: Epimeria (Drakepimeria) acanthochelon subgen. et sp. nov., E. (D.) anguloce subgen. et sp. nov., E. (D.) colemani subgen. et sp. nov., E. (D.) corbariae subgen. et sp. nov., E. (D.) cyrano subgen. et sp. nov., E. (D.) havermansiana subgen. et sp. nov., E. (D.) leukhoplites subgen. et sp. nov., E. (D.) loerzae subgen. et sp. nov., E. (D.) pandora subgen. et sp. nov., E. (D.) pyrodrakon subgen. et sp. nov., E. (D.) robertiana subgen. et sp. nov., Epimeria (Epimeriella) atalanta sp. nov., Epimeria (Hoplepimeria) cyphorachis subgen. et sp. nov., E. (H.) gargantua subgen. et sp. nov., E. (H.) linseae subgen. et sp. nov., E. (H.) quasimodo subgen. et sp. nov., E. (H.) xesta subgen. et sp. nov., Epimeria (Laevepimeria) anodon subgen. et sp. nov., E. (L.) cinderella subgen. et sp. nov., Epimeria (Pseudepimeria) amoenitas sp. nov., E. (P.) callista sp. nov., E. (P.) debroyeri sp. nov., E. (P.) kharieis sp. nov., Epimeria (Subepimeria) adeliae sp. nov., E. (S.) iota sp. nov., E. (S.) teres sp. nov. and E. (S.) urvillei sp. nov. The type specimens of E. (D.) macrodonta Walker, 1906, E. (D.) similis Chevreux, 1912, E. (H.) georgiana Schellenberg, 1931 and E. (H.) inermis Walker, 1903 are re-described and illustrated. Besides the monographic treatment of Epimeriidae from the Southern Ocean, a brief overview and identification keys are given for their putative and potential relatives from the same ocean, i.e., the Antarctic and sub-Antarctic members of the following eusiroid families: Acanthonotozomellidae Coleman & J.L. Barnard, 1991, Dikwidae Coleman & J.L. Barnard, 1991, Stilipedidae Holmes, 1908 and Vicmusiidae Just, 1990. This overview revealed the existence of a new large and characteristic species of Alexandrella Chevreux, 1911, A. chione sp. nov. but also shows that the taxonomy of that genus remains poorly known and that several ‘variable widespread eurybathic species’ probably are species complexes. Furthermore, the genera Bathypanoploea Schellenberg, 1939 and Astyroides Birstein & Vinogradova, 1960 are considered to be junior synonyms of Alexandrella. Alexandrella mixta Nicholls, 1938 and A. pulchra Ren in Ren & Huang, 1991 are re-established herein, as valid species. It is pointed out that this insufficient taxonomic knowledge of Antarctic amphipods impedes ecological and biogeographical studies requiring precise identifications. Stacking photography was used for the first time to provide iconographic support in amphipod taxonomy, and proves to be a rapid and efficient illustration method for large tridimensionally geometric species. A combined morphological and molecular approach was used whenever possible for distinguishing Epimeria species, which were often very similar (albeit never truly cryptic) and sometimes exhibited allometric and individual variations. However in several cases, taxa were characterized by morphology only, whenever the specimens available for study were inappropriately fixed or when no sequences could be obtained. A large number of Epimeria species, formerly considered as eurybathic and widely distributed, proved to be complexes of species, with a narrower (overlapping or not) distribution. The distributional range of Antarctic Epimeria is very variable from species to species. Current knowledge indicates that some species from the Scotia Arc and the tip of the Antarctic Peninsula are narrow range endemics, sometimes confined to one island, archipelago, or ridge (South Georgia, South Orkney Islands, Elephant Island or Bruce Ridge); other species have a distribution encompassing a broader region, such as the eastern shelf of the Weddell Sea, or extending from the eastern shelf of the Weddell Sea to Adélie Coast. The most widely distributed species are E. (D.) colemani subgen. et sp. nov., E. (E.) macronyx (Walker, 1906), E. (H.) inermis Walker, 1903 and E. (L.) walkeri (K.H. Barnard, 1930), which have been recorded from the Antarctic Peninsula/South Shetland Islands area to the western Ross Sea. Since restricted distributions are common among Antarctic and sub-Antarctic Epimeria, additional new species might be expected in areas such as the Kerguelen Plateau, eastern Ross Sea, Amundsen Sea and the Bellingshausen Sea or isolated seamounts and ridges, where there are currently no Epimeria recorded. The limited distribution of many Epimeria species of the Southern Ocean is presumably related to the poor dispersal capacity in most species of the genus. Indeed with the exception of the pelagic and semipelagic species of the subgenus Epimeriella, they are heavy strictly benthic organisms without larval stages, and they have no exceptional level of eurybathy for Antarctic amphipods. Therefore, stretches deeper than 1000 m seem to be efficient geographical barriers for many Epimeria species, but other isolating factors (e.g., large stretches poor in epifauna) might also be at play. The existence of endemic shelf species with limited dispersal capacities in the Southern Ocean (like many Epimeria) suggests the existence of multiple ice-free shelf or upper slope refugia during the Pleistocene glaciations within the distributional and bathymetric range of these species. Genera with narrow range endemics like Epimeria would be excellent model taxa for locating hotspots of Antarctic endemism, and thus potentially play a role in proposing meaningful Marine Protected Areas (MPAs) in the Southern Ocean.