Biochronology and paleoclimatic implications of Middle Eocene to Oligocene planktic foraminiferal faunas

Planktic foraminiferal assemblages have been analyzed quantitatively in six DSDP sites in the Atlantic (Site 363), Pacific (Sites 292, 77B, 277), and Indian Ocean (Sites 219, 253) in order to determine the nature of the faunal turnover during Middle Eocene to Oligocene time. Biostratigraphic ranges of taxa and abundance distributions of dominant species are presented and illustrate striking similarities in faunal assemblages of low latitude regions in the Atlantic, Pacific and Indian oceans. A high resolution biochronology, based on dominant faunal characteristics and 55 datum events, permits correlation between all three oceans with a high degree of precision. Population studies provide a view of the global impact of the paleoclimatic and paleoceanographic changes occurring during Middle Eocene to Oligocene time.Planktic foraminiferal assemblage changes indicate a general cooling trend between Middle Eocene to Oligocene time, consistent with previously published oxygen isotope data. Major faunal changes, indicating cooling episodes, occur, however, at discrete intervals: in the Middle Eocene 44-43 Ma (P13), the Middle/Late Eocene boundary 41-40 Ma ( ), the Late Eocene 39-38 Ma ( ), the Eocene/Oligocene boundary 37-36 Ma (P18), and the Late Oligocene 31-29 Ma ( ). With the exception of the boundary, faunal changes occur abruptly during short stratigraphic intervals, and are characterized by major species extinctions and first appearances. The Eocene/Oligocene boundary cooling is marked primarily by increasing abundances of cool water species. This suggests that the boundary cooling, which marks a major event in the oxygen isotope record affected planktic faunas less than during other cooling episodes. Planktic foraminiferal faunas indicate that the boundary event is part of a continued cooling trend which began during the Middle Eocene.Two hiatus intervals are recognized in low and high latitude sections at the Middle/Late Eocene boundary and in the Late Eocene ( ). These hiatuses suggest that vigorous bottom water circulation began developing in the Middle Eocene, consistent with the onset of the faunal cooling trend, and well before the development of the psychrosphere at the boundary.     

Cenozoic deep-sea ostracods from Maud Rise, Weddell Sea, Antarctica (ODP Site 689): a palaeoceanographical perspective

Cenozoic palaeoceanography of the Maude Rise, Weddell Sea, Antarctica, has been investigated using Palaeocene to Quaternary deep-sea ostracod faunas from 23 samples of ODP Site 689. The abundance of ostracods is high enough only during the Palaeogene (Palaeocene-Oligocene) to allow palaeoceanographical inferences based on changes in diversity, dominance, endemism and faunal turnover (first and last occurrences). The abundance is particularly high throughout the Palaeocene and Eocene, but declines irreversibly near the Eocene/Oligocene boundary. The diversity increases more or less continuously from the Early Palaeocene to the Middle Eocene, and then it generally decreases throughout the remaining part of the Palaeogene (Middle Eocene-Oligocene); an exception is a positive peak in the Shannon-Weaver index in a single sample in the Late Oligocene. No positive peaks in diversity and taxa originations (first occurrences) at c. 40-38 Ma, occurs at Site 689; so the site provides no evidence for the establishment of the psychrosphere at this time. This corroborates similar regional results from an earlier study of benthonic foraminifera. Explanations for this may be related to Late Eocene-Early Oligocene changes in sedimentology and clay-mineralogy (associated with the progressive cooling of the Antarctica) which could have negatively affected abundance and diversity locally at Site 689. Alternatively, by this time, the ostracod fauna could also have been subjected to selective removal (with possible local extinction) of taxa (due to increased ventilation) or to thanatocoenosis dissolution (due to a decrease in temperature and availability of CaCO₃). A further possibility may be related to the fact that Site 689 was at intermediate water depths and may have remained within older water masses near the Eocene/Oligocene boundary. Failing these explanations, the results could indicate that the Late Eocene-Early Oligocene palaeoenvironmental changes in the world oceans were more gradual and occurred over a longer time interval than the global ostracod data show, at least at southern high latitudes.     

Deep-sea benthonic foraminiferal faunal turnover near the Eocene/Oligocene boundary

Eocene-Oligocene deep-sea benthonic foraminifera in D.S.D.P. Site 277 in the southwest Pacific have been analyzed to determine the benthonic foraminiferal response to the development of the psychrosphere near the Eocene/Oligocene boundary. Biostratigraphic ranges of 41 taxa show that 23 taxa are found throughout the Late Eocene to Early Oligocene sequence, while 18 taxa exhibit first or last occurrences. Comparison of the faunal changes in Site 277 with a benthonic foraminiferal oxygen isotope record shows that the development of the psychrosphere did not have a profound effect upon the benthonic foraminifera, and the overall faunal change preceding and subsequent to the bottom-water circulation event occurred gradually. The inferred water-mass event affected the relative abundance of one species, Epistominella umbonifera. The lack of major faunal changes at the Eocene/Oligocene boundary in Site 277 probably reflects either wide environmental tolerances of the benthonic foraminifera, or a bottom-water temperature change less than 3°C.Examination of previously published benthonic foraminiferal biostratigraphic data from D.S.D.P. Sites 167, 171, 357, 360, 363, and 400A, and deep-sea ostracode data from D.S.D.P. Leg 3 show faunal changes occurred during discrete intervals in the Middle Eocene-Early Oligocene. The faunal patterns from these data and from Site 277 show that the Eocene/Oligocene cooling event did not cause rapid, catastrophic changes of the benthonic faunas of the open ocean, although significant faunal changes are associated with the water mass event in Sites 167, 171 and 400A.The benthonic faunal changes in Middle Eocene-Early Oligocene time are consistent with the gradual decrease of inferred bottom-water temperatures, based on previously published oxygen isotopic data. The δ ¹⁸O Eocene/Oligocene enrichment of 0.76‰ is a major event in the Southern Ocean oxygen isotopic record, but is considerably less in magnitude than the 1.75-2.00‰ change that occurred gradually from mid-Early Eocene to the Eocene/Oligocene boundary. The benthonic foraminiferal and isotopic data indicate that bottom-water circulation may have developed during the Middle Eocene to Early Oligocene interval, with the 3°C bottom-water cooling near the Eocene/Oligocene boundary representing part of this development.     

Eocene–Oligocene calcareous nannofossils from Maud Rise and Kerguelen Plateau (Antarctica): paleoecological and paleoceanographic implications

The evolution of the Southern Ocean climate during the late Eocene–late Oligocene interval is examined through high-resolution, quantitative calcareous nannofossil analyses on samples from the Southern Ocean sections on Maud Rise and Kerguelen Plateau. We determined the abundance patterns of the counted species to clarify the biostratigraphy, which we correlated with high-resolution magnetostratigraphy [Roberts, A.P., Bicknell, S.J., Byatt, J., Bohaty, S.M., Florindo, F., Harwood, D.M., 2003a. Magnetostratigraphic calibration of Southern Ocean diatom datums from the Eocene–Oligocene of Kerguelen Plateau (Ocean Drilling Program Sites 744 and 748). In: Florindo, F., Cooper, A.K., O'Brien, P.A. (Eds.), Antarctic Cenozoic Palaeoenvironments: Geologic Record and Models. Palaeogeogr., Palaeoclimatol., Palaeoecol. 198 145–168; Florindo, F., Roberts, A.P., in press. Eocene–Oligocene magnetobiochronology of ODP Sites 689 and 690, Maud Rise, Weddell Sea, Antarctica. Geol. Soc. Am. Bull.], and used this data to interpret paleoceanographic changes through the late Eocene to late Oligocene. Percentage plots of the individual species, compared with R-mode principal component and cluster analysis results, allowed us to divide the assemblages into three groups: temperate-water taxa, cool-water taxa, and no temperature-affinity taxa. We attempt correlations between these paleoecological groups and the major sea-surface temperature (SST) variations with tectonic and paleoceanographic changes in the Southern Ocean. During the late Eocene, the nannofossil assemblage data reveal that there were several minor SST decreases (coolings) from 36 to 34 Ma, before the Eocene/Oligocene (E/O) boundary. A sharp cooling event, dated at 33.54 Ma (earliest Oligocene), occurred about 160 kyr after the E/O boundary, which is dated at 33.7 Ma. Relatively stable, cool conditions are interpreted to persist until the latest Oligocene, when an increase in abundance of temperate-water taxa, which corresponds to an antithetical decrease in abundance of cool-water indicators, is recorded.On the basis of our dating, the opening of the Drake Passage, allowing shallow-water circulation, began by 33.54 Ma at the latest, while the establishment of deep-water connections through the Tasmanian Gateway occurred at 33 Ma, as suggested by Exon et al. [Proc. ODP, Init. Rep. 189 (2001) 1].     

Shallow-marine ostracode faunas around the Eocene/Oligocene boundary in the northwestern Kyushu, southwestern Japan

Middle Eocene–early Oligocene ostracode faunal changes in northwestern Kyushu of southwestern Japan are identified in this study. Ostracodes occur from shelf deposits of five formations: the middle Eocene Okinoshima, the upper Eocene Funazu, the uppermost Eocene–lowermost Oligocene Kishima, the lowermost Oligocene Itanoura, and the lower Oligocene Waita Formations. The middle Eocene–earliest Oligocene ostracodes were characterized by warm-water genera, indicating tropical, subtropical and Tethyan genera, whereas the late early Oligocene ostracodes do not include warm-water taxa, consisting of temperate realm genera. The middle Eocene–earliest Oligocene ostracodes do not include remarkable changes of species composition, in contract with equatorial Pacific radiolarians and West Coast USA molluscs. Ostracodes suggest that distinct climatic cooling did not occur in the southwestern Japan during the middle Eocene–earliest Oligocene.     

Foraminiferal turnover across the Eocene–Oligocene transition at Fuente Caldera, southern Spain: No cause–effect relationship between meteorite impacts and extinctions

We studied planktic and small benthic foraminifera from the Fuente Caldera section, southern Spain, across the Eocene–Oligocene transition. Benthic foraminifera indicate lower bathyal depths for the late Eocene and earliest Oligocene. Detailed high-resolution sampling and biostratigraphical data allowed us to date precisely layers with evidence for meteorite impact (Ni-rich spinel), which occur in the lower part of the planktic foraminiferal Globigerapsis index Biozone and in the middle part of the small benthic foraminiferal Cibicidoides truncanus (BB4) Biozone (middle Priabonian, late Eocene). Major turnovers of foraminifera occur at the Eocene/Oligocene boundary, only. The impact did not occur at a time of planktic or benthic foraminiferal extinction events, and the late Eocene meteorite impacts did thus not cause extinction of foraminifera. The most plausible cause of the Eocene/Oligocene boundary extinctions is the significant cooling, which generated glaciation in Antarctica and eliminated most of the warm and surface-dwelling foraminifera.     

A new genus and species of triggerfish from the Middle Eocene of the Northern Caucasus,the earliest member of the Balistidae (Tetraodontiformes)

Until now, the earliest known members of the triggerfish family Balistidae have been two genera from the Oligocene. Herein is described the new balistid Gornylistes prodigiosus gen. et sp. nov. from the uppermost Middle Eocene (Kuma Horizon) of the Northern Caucasus (Gorny Luch locality); it is as thoroughly modern in its bauplan as the taxa of balistids from the Oligocene and more recent periods, and far more advanced morphologically than the several stem taxa of the balistoid + ostracioid clade known from earlier in the Middle and Lower Eocene and from the Upper Paleocene.     

The Dinosauria,an updated compendium that matches its subject in scale and scope

The palaeoecology of a sequence of five closely spaced mammalian assemblages in the English Late Eocene Bembridge Limestone Formation is studied using cladistic, seriation and ecological diversity methods, after assessing the collecting and taphonomic biases. Analysis of this sequence is important as it is temporally close to the terminal Eocene global cooling event. It is concluded that the assemblages probably reflect quite closely the species composition of the original living communities and that they indicate habitats ranging from an open wooded environment to dense forest. The oldest assemblage (limestone facies) indicates open wooded habitat and contains earliest occurrences of certain taxa in the English Eocene; these represent northward dispersal from southwestern Europe in response to changing climate. The more forested habitats occur higher in the sequence and are characterised by ‘Lazarus’ taxa, suggesting reversion to earlier existing environments. Small scale changes appear to relate to local events, whereas more major ones may result from global climate change. Certain pairs of closely related species are segregated in different assemblages which are habitat distinctive, a conclusion not available from their morphologies.     

Middle Eocene–late Oligocene climate variability: Calcareous nannofossil response at Kerguelen Plateau,Site 748

A major deterioration in global climate occurred through the Eocene–Oligocene time interval, characterized by long-term cooling in both terrestrial and marine environments. During this long-term cooling trend, however, recent studies have documented several short-lived warming and cooling phases. In order to further investigate high-latitude climate during these events, we developed a high-resolution calcareous nannofossil record from ODP Site 748 Hole B for the interval spanning the late middle Eocene to the late Oligocene (~ 42 to 26 Ma). The primary goals of this study were to construct a detailed biostratigraphic record and to use nannofossil assemblage variations to interpret short-term changes in surface-water temperature and nutrient conditions. The principal nannofossil assemblage variations are identified using a temperate-warm-water taxa index (Twwt), from which three warming and five cooling events are identified within the middle Eocene to the earliest Oligocene interval. Among these climatic trends, the cooling event at ~ 39 Ma (Cooling Event B) is recorded here for the first time. Variations in fine-fraction δ¹⁸O values at Site 748 are associated with changes in the Twwt index, supporting the idea that significant short-term variability in surface-water conditions occurred in the Kerguelen Plateau area during the middle and late Eocene. Furthermore, ODP Site 748 calcareous nannofossil paleoecology confirms the utility of these microfossils for biostratigraphic, paleoclimatic, and paleoceanographic reconstructions at Southern Ocean sites during the Paleogene.     

The development of planktonic biogeography in the Southern Ocean during the Cenozoic

Deep-sea drilling at high latitudes of the Southern Hemispheres has provided almost the only available data to evaluate the biogeographic development of the planktonic biota in the Southern Ocean during the Cenozoic (65 m.y. to Present Day). Paleontological investigations on Deep Sea Drilling Project (DSDP) materials have shown that the development of Cenozoic planktonic biogeography of the Southern Ocean is intimately linked with the evolution of the Southern Ocean water masses themselves. During the Cenozoic, this has included the development of the Circum-Antarctic Current system as obstructing land masses moved apart, the refrigeration and later extensive glaciation of the continent, and the development of the Antarctic Convergence (Polar Front) with related oceanic upwelling.Almost all evolution of calcareous planktonic microfossils has occurred outside of the Antarctic—Subantarctic region followed by limited migration into these water masses. Virtually no endemism occurs amongst calcareous microfossil groups at these latitudes. In contrast, conspicuous and widespread evolution has occurred within the siliceous microfossil groups especially during the Neogene. Low diversity and differences in stratigraphic ranges of Antarctic calcareous microfossils makes them only broadly useful for correlation. Relatively higher diversities within the Subantarctic provide a firmer basis for more detailed correlation, although the ranges of fossils are often different than at lower latitudes because of different paleoceanographic and paleoclimatic controls. Within the Antarctic water mass south of the Antarctic Convergence, siliceous microfossilsbiostratigraphy, oxygen isotopic stratigraphy and magnetostratigraphy, provide the only firm basis for correlation with low-latitude sequences.Eocene (55-38 Ma) sediments contain abundant calcareous microfossils even closely adjacent to the continent. Antarctic calcareous planktonic microfossils of this age exhibit relative high diversity, although this is lower than assemblages of equivalent age at middle and low latitudes. Within the Subantarctic region, Eocene planktonic foraminifera exhibit strong affinities with those in the temperate regions. Biogeographic differences exist between various sectors of the Southern Ocean related to biogeographic isolation preceding the development of the Circum-Antarctic Current. Subantarctic calcareous nannofossil assemblages of Paleocene and Eocene age exhibit higher diversity than Oligocene and Neogene assemblages. Siliceous microfossils are poorly represented or at best poorly known.One of the most dramatic changes in Southern Ocean planktonic biogeography occurred near the Eocene/Oligocene boundary (38 Ma). Since then, Antarctic planktonic foraminiferal assemblages have exhibited distinct polar characteristics, marked in particular by low diversity, and this event thus reflects the initiation of the Antarctic faunal and floral provinces. Profound paleoceanographic changes at this time, which triggered the biogeographic crisis, appear to be related to the initiation of widespread Antarctic sea-ice formation, and rapid cooling of deep and intermediate waters, in turn associated with increased Antarctic glaciation. During the Oligocene, planktonic microfossil diversity was low in all groups throughout the world's oceans. In Antarctic waters, the early Oligocene foraminiferal fauna is monospecific (Subbotina angiporoides), while in the later Oligocene two species (S. angiporoides and Catapsydrax dissimilis) were recorded. Calcareous nannofossil assemblages are of low diversity compared with the Eocene. Subantarctic foraminiferal faunas of Oligocene age display much higher diversity than those in the Antarctic, but early and middle Oligoceae faunas still exhibit the lowest diversities for the entire Cenozoic. Siliceous assemblages remain relatively inconspicuous in most regions of the Southern Ocean.The Paleogene-Neogene transition (22 Ma) is marked by a major change in the global planktonic biogeography, i.e. modern patterns developed in which permanent, steep faunal and floral diversity gradients existed between tropical and polar regions; a gradient which has persisted even during the most severe glacial episodes. Oligocene assemblages of low diversity and almost cosmopolitan distribution were replaced by distinctive belts of planktonic assemblages arranged latitudinally from the tropics to the poles. The establishment of the steep planktonic diversity gradients and latitudinal provinces near the beginning of the Neogene almost certainly were linked to the development of the Circum-Antarctic Current in the late Oligocene which effectively separated high- and low-latitude planktonic assemblages. These fundamental global circulation and biogeographic patterns have persisted through the Neogene.During the Neogene (22 Ma to Present Day), Antarctic calcareous microfossil assemblages exhibit persistent low diversity and high dominance, while Subantarctic assemblages are of much greater diversity. The beginning of the Neogene (= beginning of Miocene) heralded the development of the high-latitude siliceous microfossil assemblages towards their present-day dominant role. Siliceous biogenec productivity began to increase. These changes were linked to the initial development and later intensification of circulation associated with the Antarctic Convergence and Antarctic Divergence. The Antarctic Convergence sharply separates dominantly siliceous assemblages to the south from calcareous assemblages to the north. Radiolarian assemblages became more endemic. Relatively warm early and middle Miocene conditions are reflected by slightly higher diversity of planktonic foraminifera and by the presence, in the northern Subantarctic, of conspicuous discoasters in early Miocene sediments. In Antarctic waters, calcareous nannofossils become unimportant as biogenic elements after the middle Miocene.The latest Miocene ( 5 m.y. ago) was marked by northward movement of the Antarctic Convergence, corresponding expansion of the Antarctic water mass, and low diversity of calcareous assemblages. Pliocene planktonic foraminifera seem to be largely monospecific in Antarctic and southern Subantarctic sequences. During the Quaternary, Antarctic waters reached a maximum northward expansion and exhibit highest siliceous biogenic productivity for the Cenozoic. In the Subantarctic, Quaternary foraminiferal diversities are much higher than in Pliocene sequences. Although calcareous nannofossil diversity may be high, only a few species are abundant. Large northward shifts of Antarctic and Subantarctic water masses have occurred during the Quaternary although no southward penetrations have occurred much beyond that of the present day. Several radiolarian and foraminiferal species disappeared or appeared at or close to a number of paleomagnetic reversals during the last 4 m.y. These faunal events, which provide valuable datums, do not seem to be associated with major climatic changes.     

Paleocene-Early Eocene ostracodes from the Southern Galala Plateau (Eastern Desert, Egypt): Taxonomy, impact of paleobathymetric changes

Ostracode faunas obtained from nine sections spanning the Paleocene-Early Eocene interval from a platform-basin transect in the Southern Galala Plateau area (Eastern Desert, Egypt) have been investigated. The study focuses on taxonomy and biostratigraphy of the ostracode assemblages across the P/E boundary, with supporting comments on paleoecology and paleobiogeography. The studied nine sections yielded 60 taxa belonging to 39 genera. Five species are new. The P/E transition is characterized by the appearance of new taxa rather than extinctions. During the Early and early Late Paleocene, the ostracode assemblages throughout the study area are largely similar, being dominated by middle-outer neritic taxa. In the late Late Paleocene and Early Eocene, changes in the paleobathymetry from deeper marine environments in the distal area in the south to shallower marine environments in the proximal area in the north become pronounced. Many of the recorded taxa have a wide geographic distribution throughout the Middle East and North Africa. Similarities with basins of West Africa are also found, reflecting faunal exchanges between this area and southern Tethys during the Paleocene and Early Eocene.     

Cenozoic record of elongate,cylindrical, deep-sea benthic foraminifera in the North Atlantic and equatorial Pacific Oceans

In the late Pliocene–middle Pleistocene a group of 95 species of elongate, cylindrical, deep-sea (lower bathyal–abyssal) benthic foraminifera became extinct. This Extinction Group (Ext. Gp), belonging to three families (all the Stilostomellidae and Pleurostomellidae, some of the Nodosariidae), was a major component (20–70%) of deep-sea foraminiferal assemblages in the middle Cenozoic and subsequently declined in abundance and species richness before finally disappearing almost completely during the mid-Pleistocene Climatic Transition (MPT). So what caused these declines and extinction?In this study 127 Ext. Gp species are identified from eight Cenozoic bathyal and abyssal sequences in the North Atlantic and equatorial Pacific Oceans. Most species are long-ranging with 80% originating in the Eocene or earlier. The greatest abundance and diversity of the Ext. Gp was in the warm oceanic conditions of the middle Eocene–early Oligocene. The group was subjected to significant changes in the composition of the faunal dominants and slightly enhanced species turnover during and soon after the rapid Eocene–Oligocene cooling event. Declines in the relative abundance and flux of the Ext. Gp, together with enhanced species loss, occurred during middle–late Miocene cooling, particularly at abyssal sites. The overall number of Ext. Gp species present began declining earlier at mid abyssal depths (in middle Miocene) than at upper abyssal (in late Pliocene–early Pleistocene) and then lower bathyal depths (in MPT). By far the most significant Ext. Gp declines in abundance and species loss occurred during the more severe glacial stages of the late Pliocene–middle Pleistocene.Clearly, the decline and extinction of this group of deep-sea foraminifera was related to the function of their specialized apertures and the stepwise cooling of global climate and deep water. We infer that the apertural modifications may be related to the method of food collection or processing, and that the extinctions may have resulted from the decline or loss of their specific phytoplankton or prokaryote food source, that was more directly impacted than the foraminifera by the cooling temperatures.     

伊朗卡尚地区古近纪介形类的发现

本文简要报道了发现于伊朗卡尚地区古近系的介形类,计16属6种、8比较种、9未定种及1亲近种。根据介形类化石组合面貌,并结合钙质超微、沟鞭藻和有孔虫化石组合,认为含介形类化石的地层时代为始新世至渐新世,推测其沉积环境为正常浅海大陆架环境,而且为温暖浅海内陆架。     

Eocene -Oligocene paleoceanography of the deep Bay of Biscay: Benthic foraminiferal evidence

A major change in benthic foraminiferal assemblages occurred in the deep Bay of Biscay (> 3 km water; DSDP Sites 119, and Site 400A) between early middle Eocene and earliest Oligocene. Predominant Eocene deep-sea taxa (Nuttallides truempyi, Clinapertina spp., Abyssamina spp.) and associated rarer species became extinct in this interval. These extinctions were followed by an increase in abundance of bathymetrically wide-ranging and stratigraphically long-ranging taxa: Globocassidulina subglobosa, Oridorsalis spp., Gyroidinoides spp., and the Cibicidoides ungerianus plexus. The extinctions cannot be dated precisely from the stratigraphic record recovered to date in the Bay of Biscay; however, the replacement of the N. truempyi-dominated assemblage has been noted previously in the deep South Atlantic/Caribbean as occurring near the middle/late Eocene boundary. Other than the decrease in abundance and extinction of N. truempyi, no major abundance changes are noted within the Eocene at the shallower Site 401 (～ 2 km water) in the Bay of Biscay. During the Oligocene, Nuttallides umbonifera replaced the Eocene species N. truempyi as the predominant deep-sea benthic foraminifera, reaching peak abundance in the middle Oligocene at Sites 119 and Site 400A. In the modern oceans, the abundance ot N. umbonifera is positively correlated with increased corrosiveness of bottom water, while at Site 119 the abundance of Nuttallides spp. is negatively correlated with δ ¹³C values in benthic foraminifera. As lower δ ¹³C values are often associated with older water masses, large numbers of Nuttallides spp. are thought to reflect older, and more corrosive bottom water. The faunal data and oxygen and carbon isotopic data are compared with a circulation model derived from North Atlantic seismic stratigraphic studies to show that old, warm, corrosive, and sluggish Eocene bottom water was replaced by younger, colder, less corrosive, more vigorously circulating bottom water of northern origin by the early Oligocene. Faunal and isotopic data suggest that bottom water became older and more corrosive again in the middle Oligocene, reflecting a reduction in circulation that can also be inferred from the seismic record in the nearby Rockall Plateau region.     

Eocene and Oligocene chitons (Polyplacophora) from the Paris and Hampshire Basins

Eocene and Oligocene chitons (Polyplacophora) from the Paris Basin of N France are described along with comparative material from the Hampshire Basin of the UK. The assemblages include eight species, five of which are new: Ischnochiton fehsei sp. nov., Stenoplax monila sp. nov., Chaetopleura gaasi sp. nov., C. abbessi sp. nov. and Tonicella lira sp. nov. Other taxa in the assemblages are Leptochiton cf. algesirensis, I. vectensis and S. anglica.     

Lutetian calcareous nannofossil events in the Agost section (Spain): implications toward a revision of the Middle Eocene biomagnetostratigraphy

This paper presents a detailed calcareous nannofossil biostratigraphy of the entire Lutetian of the Agost section (Betic Cordillera, SE Spain). This investigation integrates and improves on previous study performed through the Ypresian/Lutetian boundary by the authors on this succession. The new revision of the integrated bio‐magnetobiochronology of the Early/Middle Eocene interval revealed highly diversified calcareous nannofossil assemblages, characterizing more than 8 Myr of climatic variability. The studied interval spans from Zone CP11 to Subzone CP14a and from the upper part of Zone NP13 to the base of Zone NP16 of calcareous nannofossil standard zonations. The revision of the calcareous nannofossil content enabled the identification of numerous secondary events which greatly improved the stratigraphic resolution of this time interval. An important re‐organization of the nannoflora was observed during the Y/L transition, when Reticulofenestra and Dictyococcites (Noelaerhabdaceae) became the most important genera in terms of abundance and dispersal, dominating the Middle Eocene nannofossil assemblages and replacing Toweius and Discoaster taxa characteristic of the lower Eocene. Pentaliths and Blackites experience a great expansion and diversification, whereas Discoaster and Chiasmolithus which are well diversified but never abundant during the Lutetian show a slow turnover. A reassessment of the major bio‐events observed in the Noelaerhabdaceae family as well as revision and correlation of these events with the classical Italian sections (Contessa and Bottaccione) are presented. The new results show that biostratigraphic problems related to the Middle Eocene chronology are not limited to the correlation between calcareous nannofossils and planktonic foraminiferans at the Y/L transition but extend to calcareous nannofossil events commonly used for correlating the Bartonian.     

Diets of fossil primates from the Fayum Depression of Egypt: a quantitative analysis of molar shearing

Over the last 90 years, Eocene and Oligocene aged sediments in the Fayum Depression of Egypt have yielded at least 17 genera of fossil primates. However, of this diverse sample the diets of only four early Oligocene anthropoid genera have been previously studied using quantitative methods. Here we present dietary assessments for 11 additional Fayum primate genera based on the analysis of body mass and molar shearing crest development. These studies reveal that all late Eocene Fayum anthropoids were probably frugivorous despite marked subfamilial differences in dental morphology. By contrast, late Eocene Fayum prosimians demonstrated remarkable dietary diversity, including specialized insectivory (Anchomomys), generalized frugivory (Plesiopithecus), frugivory+insectivory (Wadilemur), and strict folivory (Aframonius). This evidence that sympatric prosimians and early anthropoids jointly occupied frugivorous niches during the late Eocene reinforces the hypothesis that changes in diet did not form the primary ecological impetus for the origin of the Anthropoidea. Early Oligocene Fayum localities differ from late Eocene Fayum localities in lacking large-bodied frugivorous and folivorous prosimians, and may document the first appearance of primate communities with trophic structures like those of extant primate communities in continental Africa. A similar change in primate community structure during the Eocene-Oligocene transition is not evident in the Asian fossil record. Putative large anthropoids from the Eocene of Asia, such as Amphipithecus mogaungensis, Pondaungia cotteri, and Siamopithecus eocaenus, share with early Oligocene Fayum anthropoids derived features of molar anatomy related to an emphasis on crushing and grinding during mastication. However, these dental specializations are not seen in late Eocene Fayum anthropoids that are broadly ancestral to the later-occurring anthropoids of the Fayum's upper sequence. This lack of resemblance to undisputed Eocene African anthropoids suggests that the "progressive" anthropoid-like dental features of some large-bodied Eocene Asian primates may be the result of dietary convergence rather than close phyletic affinity with the Anthropoidea.     

Fish otoliths from the Priabonian (Late Eocene) of North Italy and South-East France - Their paleobiogeographical significance

The study of the Late Eocene (Priabonian) otolith associations from Possagno, North-East Italy, and from the Synclinal d’Allons in Haute Provence, South-East France, allows for the reconstruction of a teleost fauna of 55 taxa, which is the most diversified assemblage presently known from the Upper Eocene Paleo-Mediterranean basin. Thirty-six taxa are identified at the species level, and five of those are new: “genus Alepocephalidarum” astrictus, “genus Lophiiformorum” canovae, “genus Agonidarum” sudans, “genus Uranoscopidarum” cochlearis and Aseraggodes laganum. In the Synclinal d’Allons, the otolith associations reflect a tropical to subtropical neritic environment with a few mesopelagic fishes. At Possagno, the associations indicate an environment that changed from one that was deep and exposed to the pelagic realm and then evolved to a more shallow sea with a well-diversified benthic life and less mesopelagic fishes. A paleobiogeographical analysis of all known data on Priabonian otoliths, worldwide, shows clearly a western Atlantic (Louisiana) and an eastern Atlantic-Paleomediterranean association. In the eastern Atlantic-Paleomediterranean association, the Aquitaine association not only differs from the Possagno-Allons association in function of its more distant geographical position, but also by its stronger oceanic character in the southern part of the basin, and by the occurrence in the north, of a very shallow water facies (Saint-Estephe Formation) that contains some taxa which are known nowhere else in the Priabonian. The Ukraine fauna is characterized by a high number of species, which have an Oligocene record in other European sites. The northern geographic location of Ukraine, combined with the good connections to both the North Sea Basin and the Turgai street can provide the explanation. Many Oligocene species (or their close relatives) probably already existed at Eocene times in more northern regions, but could penetrate only in more southern European seas since the strong cooling at the beginning of the Oligocene.     

Stepwise mass extinctions and impact events: Late Eocene to early Oligocene

Species ranges and relative abundances of dominant planktonic foraminifers of eight late Eocene to early Oligocene deep-sea sections are discussed to determine the nature and magnitude of extinctions and to investigate a possible cause-effect relationship between impact events and mass extinctions.Late Eocene extinctions are neither catastrophic nor mass extinctions, but occur stepwise over a period of about 1–2 million years. Four stepwise extinctions are identified at the middle/late Eocene boundary, the upperGlobigerapsis semiinvoluta zone, theG. semiinvoluta/Globorotalia cerroazulensis zone boundary and at the Eocene/Oligocene boundary. Each stepwise extinction event represents a time of accelerated faunal turnover characterized by generally less than 15% species extinct and in itself is not a significant extinction event. Relative species abundance changes at each stepwise extinction event, however, indicate a turnover involving > 60% of the population implying major environmental changes.There microtektite horizons are present in late Eocene sediments; one in the upperG. semiinvoluta zone (38.2 Ma) and two closely spaced layers only a few thousand years apart in the lower part of theGloborotalia cerroazulensis zone (37.2 Ma). Each of the three impact events appears to have had some effect on microplankton communities. However, the overriding factor that led to the stepwise mass extinctions may have been the result of multiple causes as there is no evidence of impacts associated with the step preceding, or the step following the deposition of the presently known microtektite horizons.     

Middle Eocene–Early Pliocene Subantarctic planktic foraminiferal biostratigraphy of Site 1090, Agulhas Ridge

The analysis of planktic foraminiferal assemblages from Site 1090 (ODP Leg 177), located in the central part of the Subantarctic Zone south of South Africa, provided a geochronology of a 330-m-thick sequence spanning the Middle Eocene to Early Pliocene. A sequence of discrete bioevents enables the calibration of the Antarctic Paleogene (AP) Zonation with lower latitude biozonal schemes for the Middle–Late Eocene interval. In spite of the poor recovery of planktic foraminiferal assemblages, a correlation with the lower latitude standard planktic foraminiferal zonations has been attempted for the whole surveyed interval. Identified bioevents have been tentatively calibrated to the geomagnetic polarity time scale following the biochronology of Berggren et al. (1995). Besides planktic foraminiferal bioevents, the disappearance of the benthic foraminifera Nuttallides truempyi has been used to approximate the Middle/Late Eocene boundary. A hiatus of at least 11.7 Myr occurs between 78 and 71 m composite depth extending from the Early Miocene to the latest Miocene–Early Pliocene. Middle Eocene assemblages exhibit a temperate affinity, while the loss of several planktic foraminiferal species by late Middle to early Late Eocene time reflects cooling. During the Late Eocene–Oligocene intense dissolution caused impoverishment of planktic foraminiferal assemblages possibly following the emplacement of cold, corrosive bottom waters. Two warming peaks are, however, observed: the late Middle Eocene is marked by the invasion of the warmer water Acarinina spinuloinflata and Hantkenina alabamensis at 40.5 Ma, while the middle Late Eocene experienced the immigration of some globigerinathekids including Globigerinatheka luterbacheri and Globigerinatheka cf. semiinvoluta at 34.3 Ma. A more continuous record is observed for the Early Miocene and the Late Miocene–Early Pliocene where planktic foraminiferal assemblages show a distinct affinity with southern mid- to high-latitude faunas.