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.     

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.     

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.     

Palaeoceanographical changes recorded by Cenozoic deep-sea ostracod assemblages from the South Atlantic and the Southern Ocean (ODP Sites 1087 and 1088)

Cenozoic palaeoceanography of the SE Atlantic and Southern Oceans has been investigated using Late Eocene/Early Oligocene to Quaternary ostracod assemblages from 49 samples of ODP Sites 1087 and 1088. Although the overall abundance of ostracods is relatively low (means of 17 and 49 specimens per sample at Sites 1087 and 1088, respectively) and there is an apparently high level of endemism (ranging from 50% to 80% at Sites 1087 and 1088), three major changes in the faunal assemblages are identified at Site 1087 (denoted A, B and C) and two at Site 1088 (denoted B' and C'). The assemblage boundaries, detected on the basis of stepwise changes in the abundance, diversity, dominance, endemism, faunal turnover and relative abundance of common taxa, coincide broadly with previously identified, ostracod-based palaeoceanographical 'events' discussed by Benson and co-workers over the last two decades. The data do not extend sufficiently far back to record the initiation of Assemblage A, but the faunal change between Assemblages A and B, marked by a decline in abundance, species diversity and faunal turnover, occurs within the Middle Miocene (NN5-6). It coincides with a previously documented palaeoceanographical 'event' at 16-14 Ma which, we suggest, may be related to the initiation of North Atlantic Deep Water (NADW) production and/or an expansion of the East Antarctic ice sheet. Assemblage B' is subdivided into the two Sub-assemblages B'¹ and B'² mainly on the basis of an increase in diversity, a peak in faunal turnover and a drop in the relative abundance of the genus Krithe in early Late Miocene time (NN9, c. 10.5 Ma). The B'¹/B'² Sub-assemblage boundary cannot be related to any previously documented faunal change in deep-sea ostracods. Changes associated with the boundaries between Assemblages B and C, and B' and C', which we believe to be synchronous, both include a decrease in diversity and abundance. In addition, two strong turnover peaks occur near the B'/C' boundary at Site 1088. The B/C and B'/C' boundaries coincide with a previously documented midPliocene 'event' (3.5 Ma) (NN15-16) which may be linked to putative closure of the Straits of Panama and increased production of NADW, the latter in turn leading to increased production of Antarctic Intermediate Water (AAIW) and Antarctic Bottom Water (AABW). Alternatively, fiuctuations in size of the Antarctic ice sheet during possible Pliocene warm periods could indirectly be responsible for the observed midPliocene faunal changes.     

Mountain uplift explains differences in Palaeogene patterns of mammalian evolution and extinction between North America and Europe

Patterns of late Palaeogene mammalian evolution appear to be very different between Eurasia and North America. Around the Eocene–Oligocene (EO) transition global temperatures in the Northern Hemisphere plummet: following this, European mammal faunas undergo a profound extinction event (the Grande Coupure), while in North America they appear to pass through this temperature event unscathed. Here, we investigate the role of surface uplift to environmental change and mammalian evolution through the Palaeogene (66–23 Ma). Palaeogene regional surface uplift in North America caused large-scale reorganization of precipitation patterns, particularly in the continental interior, in accord with our combined stable isotope and ecometric data. Changes in mammalian faunas reflect that these were dry and high-elevation palaeoenvironments. The scenario of Middle to Late Eocene (50–37 Ma) surface uplift, together with decreasing precipitation in higher-altitude regions of western North America, explains the enigma of the apparent lack of the large-scale mammal faunal change around the EO transition that characterized western Europe. We suggest that North American mammalian faunas were already pre-adapted to cooler and drier conditions preceding the EO boundary, resulting from the effects of a protracted history of surface uplift.     

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.     

Innovations among Paleogene planktonic foraminifera

Comparison of results from ODP Sites in the Indian and Antarctic Oceans with published data, reveal that planktonic foraminifera underwent considerable radiation, diversification, proliferation and expansion, throughout the 21 Myr duration of the Eocene, the longest, warmest epoch of the Cenozoic.

Fundamental changes in wall texture and test architecture occurred in equatorial, tropical, temperate, austral and boreal oceans.

One hundred new species appeared, 83 of them in tropical waters, mainly within the first eight of eleven biozones.

Lineages in the evolving continuum of Morozovella in the tropics and Acarinina in high latitudes contributed to the proliferation of muricate taxa.

Cosmopolitanism in the warm oceans of the Early‐Middle Eocene was followed by declining diversity in the Late Eocene when temperate species expanded into the tropics.

Slow taxonomic evolution continued throughout the 13 Myr duration of the Oligocene, within five zones. Provincialism in the cooling oceans was followed by progressive and iterative evolution of new lineages.

Innovative morphologies are illustrated for Pseudohastigerina, Globigerinatheka, Hantkenina, Turborotalia, Globigerina and Tenuitella.     

Facies dynamics in Eocene to Oligocene circumalpine carbonates

A new concept, termed ‘Facies Dynamics’ (defined as changes of specific carbonate facies types in time and space, which are controlled by phylogenetic, ecological and geological parameters), is introduced. This concept aims to define and interpret spatial and temporal changes of carbonate facies patterns. It is based on Middle Eocene to Early Oligocene shallow-water carbonate facies types from the circumalpine area (north-eastern Italy, northern Slovenia, Austria and southern Bavaria), which are compared with respect to dominating biogenic components and their distributions along a shelf gradient. This comparison has lead to the distinction and definition of 14 Major Facies Types (MFTs), which are dominated by coralline algae, larger and smaller foraminifera, corals and bryozoans. The presence and distribution of these MFTs from three different time slices (Middle Eocene, Late Eocene and Early Oligocene) is compared. Nine aspects of facies dynamics are distinguished: origination, extinction, immigration, emigration, expansion, reduction, stasis, shift, and replacement of MFTs. These changes are controlled by regional changes in ecological parameters, but also by global events, especially extinction patterns at the Middle/Late Eocene boundary and at the Eocene/Oligocene boundary.     

Benthic foraminiferal response to the emergence of the Isthmus of Panama and coincident paleoceanographic changes

Late Cenozoic benthic foraminiferal faunas from the Caribbean Deep Sea Drilling Project (DSDP) Site 502 (3052 m) and East Pacific DSDP Site 503 (3572 m) were analyzed to interpret bottom-water masses and paleoceanographic changes occurring as the Isthmus of Panama emerged. Major changes during the past 7 Myr occur at 6.7–6.2, 3.4, 2.0, and 1.1 Ma in the Caribbean and 6.7–6.4, 4.0–3.2, 2.1, 1.4, and 0.7 Ma in the Pacific. Prior to 6.7 Ma, benthic foraminiferal faunas at both sites indicate the presence of Antarctic Bottom Water (AABW). After 6.7 Ma benthic foraminiferal faunas indicate a shift to warmer water masses: North Atlantic Deep Water (NADW) in the Caribbean and Pacific Deep Water (PDW) in the Pacific. Flow of NADW may have continued across the rising sill between the Caribbean and Pacific until 5.6 Ma when the Pacific benthic foraminiferal faunas suggest a decrease in bottom-water temperatures. After 5.6 Ma deep-water to intermediate-water flow across the sill appears to have stopped as the bottom-water masses on either side of the sill diverge.The second change recorded by benthic foraminiferal faunas occurs at 3.4 Ma in the Caribbean and 4.0-3.2 Ma in the Pacific. At this time the Caribbean is flooded with cold AABW, which is either gradually warmed or is replaced by Glacial Bottom Water (GBW) at 2.0 Ma and by NADW at 1.1 Ma. These changes are related to global climatic events and to the depth of the sill between the Caribbean and Atlantic rather than the rising Isthmus of Panama. Benthic foraminiferal faunas at East Pacific Site 503 indicate a gradual change from cold PDW to warmer PDW between 4.0 and 3.2 Ma. The PDW is replaced by the warmer, poorly oxygenated PIW at 2.1 Ma. Although the PDW affects the faunas during colder intervals between 1.4 and 0.7 Ma, the PIW remains the principal bottom-water mass in the Guatemala Basin of the East Pacific.     

Radiolarian faunal turnover across the Oligocene/Miocene boundary in the equatorial Pacific Ocean

The global warming trend of the latest Oligocene was interrupted by several cooling events associated with Antarctic glaciations. These cooling events affected surface water productivity and plankton assemblages. Well-preserved radiolarians were obtained from upper Oligocene to lower Miocene sediments at Ocean Drilling Program (ODP) Leg 199 Sites 1218 and 1219 in the equatorial Pacific, and 110 radiolarian species were identified.Four episodes of significant radiolarian faunal changes were identified: middle late Oligocene (27.5 to 27.3 Ma), latest Oligocene (24.4 Ma), earliest Miocene (23.3 Ma), and middle early Miocene (21.6 Ma). These four episodes approximately coincide with increases and decreases of biogenic silica accumulation rates and increases in δ¹⁸O values coded as “Oi” and “Mi” events. These data indicate that Antarctic glaciations were associated with change of siliceous sedimentation patterns and faunal changes in the equatorial Pacific.Radiolarian fauna was divided into three assemblages based on variations in radiolarian productivity, species richness and the composition of dominant species: a late Oligocene assemblage (27.6 to 24.4 Ma), a transitional assemblage (24.4 to 23.3 Ma) and an early Miocene assemblage (23.3 to 21.2 Ma). The late Oligocene assemblage is characterized by relatively high productivity, low species richness and four dominant species of Tholospyris anthophora, Stichocorys subligata, Lophocyrtis nomas and Lithelius spp. The transitional assemblage represents relatively low values of productivity and species richness, and consists of three dominant species of T. anthophora, S. subligata and L. nomas. The characteristics of the early Miocene assemblage are relatively low productivity, but high species richness. The two dominant species present in this assemblage are T. anthophora and Cyrtocapsella tetrapera. The most significant faunal turnover of radiolarians is marked at the boundary between the transitional/early Miocene assemblages.We also reviewed changes in other microfossil assemblages in the low latitudes during the late Oligocene through early Miocene. The microfossil assemblages of major groups show sequential changes near the Oligocene/Miocene (O/M) boundary (23.8 Ma). Many extinction events and some first occurrences of calcareous nannofossils and many occurrences of radiolarians are found from about 24.8 to 23.3 Ma, and first occurrences of planktic foraminifers and diatoms followed from 23.2 through 22 Ma. Hence, the O/M boundary is identified as a significant level for microfossil evolutions.     

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.     

Differences between the late eocene foraminiferal faunas in western und eastern Europe

During the Late Eocene two marine provinces existed in the epicontinental Europe: a West European province with a warm water foraminiferal fauna of Tethyan character and an East European province with a cold water fauna. The boundary between these provinces was situated in Poland. The main dispersion routes of the Late Eocene foraminiferal faunas coincide with some important tectonic features.     

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.     

Regional differences in pelagic productivity in the late Eocene to early Oligocene—a comparison of southern high latitudes and lower latitudes

Paleoproductivity patterns at the Eocene-Oligocene boundary in southern high latitudes and in the equatorial oceans were synthesized from the literature. Three ODP/DSDP sites from the Southern Ocean (Sites 689, 748 and 511) were compared with three DSDP/ODP sites from the equatorial oceans (Sites 574, 462 and 959). Paleoproductivity was estimated by multiple sedimentological, biological and geochemical proxies. Changes in paleoproductivity at the Eocene-Oligocene boundary mainly took place in the southern high latitudes. At Site 689, the benthic foraminiferal fauna also indicates an increase in seasonality. In equatorial oceans, there are no indications for a shift to higher paleoproductivity at the Eocene-Oligocene boundary. On the contrary at Site 959, sedimentology documents decreasing paleoproductivity in the Oligocene. Major changes in temperature and ocean circulation in southern high latitudes versus only minor changes in the lower latitudes were probably responsible for the geographically different changes in paleoproductivity.     

Paleocene-Pleistocene benthic foraminiferal evidence of major paleoceanographic events in the eastern South Atlantic (DSDP Site 525, Walvis Ridge)

Benthic foraminifers in the size-fraction greater than 0.073 mm were studied in 88 Paleocene to Pleistocene samples from Deep Sea Drilling Project Site 525 (Hole 525A, Walvis Ridge, eastern south Atlantic). Clustering of the samples on the basis of the 86 most abundant foraminifers (in total, 331 taxa were identified) allowed separating two major assemblage zones: the Paleocene to Eocene interval, and the Oligocene to Pleistocene interval. Each of these, in turn, were subdivided into three minor subzones as follows: lower upper Paleocene (approx. 62.4 to 57.8 Ma); upper upper Paleocene (56.6 to 56.2 Ma); lower and middle Eocene (55.3 to 46.8 Ma); upper Oligocene to middle Miocene (25.3 to 16 Ma); middle Miocene to Pliocene (15.7 to 4.2 Ma); and lower Pleistocene (0.4 to 0.02 Ma), with only minor differences with the previous zone. Some very abundant taxa span most of the column studies (Bolivina huneri, Cassidulina subglobosa, Eponides bradyi, E. weddellensis, Gavelinella micra, Oridorsalis umbonatus, etc.). Several of the faunal breaks recorded coincide with conspicuous minima in the specific diversity curve, thus suggesting that the corresponding turnovers signal the final stages of periods of faunal impoverishment. At least one major bottom-water temperature drop (as derived from δ¹⁸O data) is synchronous with a decrease in the foraminiferal specific diversity. On the other hand, a specific diversity maximum in the middle Miocene might be associated with a δ¹³C increase at approx. 16 to 12 Ma. Highest foraminiferal abundances (up to 600–800 individuals per gram of dry sediment) occurred in the late Paleocene and in the early Pleistocene, in coincidence with the lowest diversity figures calculated. The magnitude of the most important faunal turnover recorded, between the middle Eocene and the late Oligocene, is magnified in our data set by the large hiatus which separates the middle Eocene from the upper Oligocene sediments. Considerably smaller overturns occurred within the late Paleocene (in coincidence with changes in the specific diversity, absolute abundance of foraminiferal tests, and δ¹³C), and in the middle Miocene (in coincidence with a specific diversity maximum and a δ¹³C excursion). New information on the morphology and the stratigraphic ranges of several species is furnished. For all the taxa recorded the number of occurrences, total number of individuals identified and first and last appearances are listed.     

MIDDLE EOCENE REFRIGERATION — NEW EVIDENCE FROM CALIFORNIA PLANKTONIC FORAMINIFERAL ASSEMBLAGES

In California, faunal parameters of planktonic foraminiferal assemblages change dramatically at the Lower-Middle Eocene boundary. By analogy with modern distributional data, these changes are interpreted to reflect alteration of the prevailing water-mass character from warm-temperate to temperate. The change from warm-temperate to temperate planktonic foraminiferal assemblages occurring over the California continental borderland is reconcilable with a minimum southward displacement of 15° latitude in water-mass boundaries and lends support to the concept of a bipolar Middle Eocene refrigeration.     

Small mammal (rodents and lagomorphs) European biogeography from the Late Oligocene to the mid Pliocene

Aim To analyse the fossil species assemblages of rodents and lagomorphs from the European Neogene in order to assess what factors control small mammal biogeography at a deep‐time evolutionary time‐scale. Location Western Europe: 626 fossil‐bearing localities located within 31 regions and distributed among 18 successive biochronological units ranging from c. 27 Ma (million years ago; Late Oligocene) to c. 3 Ma (mid Pliocene). Methods Taxonomically homogenized pooled regional assemblages are compared using the Raup and Crick index of faunal similarity; then, the inferred similarity matrices are visualized as neighbour‐joining trees and by projecting the statistically significant interregional similarities and dissimilarities onto palaeogeographical maps. The inferred biogeographical patterns are analysed and discussed in the light of known palaeogeographical and palaeoclimatic events. Results Successive time intervals with distinct biogeographical contexts are identified. Prior to c. 18 Ma (Late Oligocene and Early Miocene), a relative faunal homogeneity (high interregional connectivity) is observed all over Europe, a time when major geographical barriers and a weak climatic gradient are known. Then, from the beginning of the Middle Miocene onwards, the biogeography is marked by a significant decrease in interregional faunal affinities which matches a drastic global climatic degradation and leads, in the Late Miocene (c. 11 Ma), to a marked latitudinal pattern of small mammal distribution. In spite of a short rehomogenization around the Miocene/Pliocene boundary (6–4 Ma), the biogeography of small mammals in the mid Pliocene (c. 3 Ma) finally closely reflects the extant situation. Main conclusions The resulting biogeographical evolutionary scheme indicates that the extant endemic situation has deep historical roots corresponding to global tectonic and climatic events acting as primary drivers of long‐term changes. The correlation of biogeographical events with climatic changes emphasizes the prevalent role of the climate over geography in generating heterogeneous biogeographical patterns at the continental scale.     

Ocean basin and depth variability of oxygen isotopes in cenozoic benthic foraminifera

One of the longest, most detailed quantitative records of oceanographic change in the Cenozoic is that provided by oxygen isotope measurements made on the tests of foraminifera. As indicated by measurements on benthic foraminifera, the deep waters of the world ocean have undergone an overall cooling of about 10°C in the Cenozoic. This change has been neither monotonic nor gradual. Rather, it is evidenced by a few, relatively rapid increases in the ¹³O content of the benthic shells. These “steps” in the isotopic record have been associated with major evolutionary changes in the mean state of the deep ocean. The variance around this mean state has also changed through the Cenozoic. From relatively high variance in the Middle Eocene, the oceans showed low variance in the Late Eocene and Oligocene. In the Miocene the variance of the isotopic measurement again increased, reaching a maximum of short duration in the Middle Miocene. This maximum as well as that which occurred during the Late Pliocene and Quaternary, may be attributable to fluctuations in the isotopic composition of the oceans caused by growth and decay of large ice sheets.In the Late Miocene the benthic oxygen isotopes in Atlantic sites less than 3000 m deep have a higher variance than sites at similar depths in the Pacific and Indian Oceans. It is thought that this high variance results from long-term changes in the importance of the cool and salty North Atlantic Deep Water relative to that of the warmer and less saline Antarctic Intermediate Water at Atlantic sites between 1000 m and 3000 m water depth. Such significant differences in benthic isotopic variance between the ocean basins have been demonstrated only in post-Middle Miocene intervals.     

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.