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.     

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.     

Correlation between the Paleocene/Eocene boundary and the Ilerdian at Campo, Spain

The Ilerdian is a well-established Tethyan marine stage, which corresponds to an important phase in the evolution of larger foraminifera not represented in the type-area of the classical Northwest-European stages. This biostratigraphic restudy of its parastratotype in the Campo Section (northeastern Spain) based on planktic foraminifera, calcareous nannofossils, dinoflagellate cysts and the distribution of the stable isotopes ∂¹³C and ∂¹⁸O is an attempt to correlate the Paleocene/Eocene boundary based on a characteristic carbon isotope excursion (CIE) marking the onset of the Initial Eocene Thermal Maximum (IETM) and the Ilerdian stage. The base of this ∂¹³C excursion has been chosen as the criterion for the recent proposal of the Global Stratotype Section and Point (GSSP) of the base of the Eocene (= base of the Ypresian) in the Dababiya Section (Egypt) to which an age of 54.9 Ma has been attributed. This level is also characterized by a marked extinction among the deep-water benthic foraminifera (Benthic Foraminifera Extinction Event, BFEE), a flood of representatives of the planktic foraminiferal genus Acarinina and the acme of dinoflagellate cysts of the genus Apectodinium. In the Campo Section, detailed biozonations (planktic foraminifera, calcareous nannofossils, dinoflagellate cysts) are recognized in the Lower and Middle Ilerdian. The correlation with the Ypresian stratotype is based on dinoflagellate cysts and calcareous nannofossils. The base of the Ilerdian is poor in planktic microfossils and its precise correlation with the redefined Paleocene/Eocene boundary remains uncertain.     

Facies,paleoenvironment, carbonate platform and facies changes across Paleocene Eocene of the Taleh Zang Formation in the Zagros Basin,SW-Iran

The Paleocene–Eocene Taleh Zang Formation of the Zagros Basin is a sequence of shallow-water carbonates. We have studied carbonate platform, sedimentary environments and its changes based on the facies analysis with particular emphasis on the biogenic assemblages of the Late Paleocene Sarkan and Early Eocene Maleh kuh sections. In the Late Paleocene, nine microfacies types were distinguished, dominated by algal taxa and corals at the lower part and larger foraminifera at the upper part. The Lower Eocene section is characterised by 10 microfacies types, which are dominated by diverse larger foraminifera such as alveolinids, orbitolitids and nummulitids. The Taleh Zang Formation at the Sarkan and Maleh kuh sections represents sedimentation on a carbonate ramp.

The deepening trends show a gradual increase in perforate foraminifera, the deepest environment is marked by the maximum occurrence of perforate foraminifers (Nummulites), while the shallowing trends are composed mainly of imperforate foraminifera and also characterised by lack of fossils in tidal flat facies.

Based on the facies changes and platform evolution, three stages are assumed in platform development: I; algal and coralgal colonies (coralgal platform), II; coralgal reefs giving way to larger foraminifera, III; dominance of diverse and newly developing larger foraminifera lineages in oligotrophic conditions.     

Lignites of Kutch,western India: Dinoflagellate biostratigraphy and palaeoclimate

The Eocene epoch in the Indian subcontinent was marked by widespread deposition of lignite and coal. While several of these deposits formed during the Early Eocene, corresponding to Early Eocene hyperthermal events, the lignites of Kutch in western India formed later during the Middle Eocene. An integrated biostratigraphy based on dinoflagellates and foraminifera assigns a Bartonian age to the succession, which likely corresponds to the time of the Middle Eocene warming. The spores, pollen, dinoflagellates and foraminifera suggest a restricted marine, near shore depositional environment adjacent to tropical rainforest. The lignites of Kutch suggest high precipitation during or just preceding the warm climate of the Middle Eocene.     

Mid-eocene climatic change,Southwestern California and Northwestern Baja California

A widespread paleosol of Paleocene and Early Eocene age occurs in southwestern California and northwestern Baja California. The dominant quartz-kaolinite mineralogy and cation-depleted chemistry of the buried soil indicate a humid, tropical paleoclimate similar to the modern equatorial belt. Although the Paleocene—Eocene paleomagnetic latitudes are similar to the modern latitudes (36–37°N to 32–33°N, respectively), rainfall was about 125–190 cm per year and average annual temperature was about 20–25°C in marked contrast to the present annual rainfall of 25 cm and average annual temperature of 16°C.A variety of indicators in the Late Eocene sedimentary succession suggests a change to a semi-arid paleoclimate. The nonmarine portions of the Late Eocene sedimentary record are dominated by a cobble conglomerate lithosome deposited in fluvial, alluvial fan and fan delta systems. Intertongued with the conglomerate is a sandstone lithosome deposited in flood-plain and nearshore marine environments. The conglomerate clasts were transported to the depositional site via a long-distance (200–300 km), moderate gradient, braided river system mostly by flash floods. Characteristic post-depositional, in situ fracturing of conglomerate clasts probably occurred due to salt crystallization.Within the flood plain sandstones, and to a lesser degree the conglomerates, are multiple well-developed caliche horizons of probable pedogenic origin. Clay minerals from the Late Eocene rocks are dominantly vermiculite and smectite with lesser chlorite and illite; this is in marked contrast to the kaolinite that comprises the underlying Early Paleogene lateritic paleosol.The character of the Late Eocene sedimentary succession indicates a semi-arid climate. Rainfall probably did not exceed 63 cm per year; it probably was seasonal and by occasional flash floods. This paleoclimate contrasts markedly with the earlier humid tropical paleoclimate and must indicate a widespread climatic change in late Middle Eocene time.     

Changes in the composition of the European snake fauna during the Early Miocene and at the Early / Middle Miocene transition

The members of the ‘modern’ snake families Colubridae, Viperidae and Elapidae (representatives of the family Colubridae appeared in Europe as the first) might have penetrated into the areas of Central Europe probably across the Mazury -Mazowsze continental bridge. The ‘modern’ families penetrated into West Europe across the Rhine Graben by several immigration waves. Based on the known marine incursions into the Rhine Graben and adjacent areas, a total of four distinct waves of dispersal of both the Asiatic and North American immigrants can be discerned within the Early Oligocene — Middle Miocene time span. The Early Miocene (MN 1–MN 2a) and the Early / Middle Miocene (MN 3–MN 4/5) dispersals of snakes are responsible for the final displacement of representatives of the ‘ancient’ family Boidae out of West and Central Europe. The Early and the Middle Miocene migrations have likewise initiated the evolution of the modern European snake fauna.     

Paleoecological patterns in molluscan extinctions and recoveries: comparison of the Cretaceous-Paleogene and Eocene-Oligocene extinctions in North America

Exposures across the Cretaceous-Tertiary (K-T) and Eocene-Oligocene (E-O) boundaries, in Texas and Mississippi, respectively, probably represent the most complete and best-preserved fossil molluscan sequences across these boundary intervals in the world. Outcrops from both boundaries contain pristine aragonitic and calcitic molluscan shells, which were deposited in fine-grained sediments from open marine environments. The K-T and the E-O extinctions exhibit very different recovery patterns, probably reflecting very different causes as well as magnitudes of extinction.The K-T sequence contains a molluscan fossil record that is consistent with an abrupt extinction event at the K-T boundary and a prolonged initial recovery in hostile oceanographic conditions. The uppermost 10 m of Upper Cretaceous sediments contain a diverse (approximately 40 species) molluscan fauna dominated by suspension feeders. The earliest Paleocene sediments immediately above the tsunami bed contain an impoverished fauna dominated by deposit feeders. The Paleocene fauna slowly climbs in diversity but remains relatively impoverished and dominated by deposit feeders for several hundred thousand years after the extinction in conjunction with anomalous δ¹³C values that suggest prolonged suppression of marine primary productivity. Diverse suspension-feeder dominated molluscan assemblages reappear with the resumption of normal conditions of primary production. In the long term, early to middle Paleocene gamma diversity includes evolutionary “bloom taxa,” families that exhibit unusual speciation bursts that subside in the Eocene. Total diversity for the Gulf Coast does not approach Cretaceous levels until the Late Eocene representing a total recovery interval of nearly 25 million years.While the E-O event also reflects a molluscan extinction rate of over 90% in the Gulf of Mexico, there are no signs of hostile environmental conditions in the recovery fauna. Early Oligocene molluscan assemblages are diverse and dominated by suspension feeders characteristic of normal marine conditions. The hiatus at the E-O boundary, however, could have obscured a short-term recovery fauna. There is also no sign of long-term perturbation by the E-O extinction. There are no bloom taxa and gamma diversity approaches pre-extinction levels within a few million years. The overall pattern of the E-O extinction is consistent with extinction (and/or migration) associated with long-term cooling.     

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.     

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.     

Facies distribution patterns of some marine benthic faunas in early paleozoic platform environments

Worldwide Late Cambrian—Silurian lithofacies patterns indicate that the platforms of that time were sites of accumulation of two essentially different rocks suites: the platform carbonate rocks and the platform terrigenous rocks. Most of the platform rocks accumulated as sediments in shallow marine environments similar to those of the present but far more widely spread.Present-day marine benthic faunas are distributed in depth zones which are primarily controlled by temperature. Faunas tend to occur in substrate-related discrete clusters (communities) within each life zone; similar substrates in different depth zones commonly have different faunal associations. Individual phyletic stocks may encounter environmental optimum or near-optimum conditions in certain areas, that commonly are revealed by an abundance of species and individuals within species in each stock. Environmental optimum conditions depend upon availability of food that may be utilized, modes of feeding of the animals present, water motion, and substrate, among other factors. Organisms in past seas were distributed in patterns similar to those of the present.Carbonate platforms were particularly widespread during the latest Cambrian—Early Ordovician. Intertidal environments spread widely across those platforms during that time and characteristic faunal associations developed in them. Saukiid and related tribolites dominated latest Cambrian carbonate platform intertidal faunas. The Early Ordovician carbonate platform intertidal was dominated by archeogastropod-nautiloid cephalopod faunas. These animals were joined by tabulate corals and certain brachiopods during the latter part of the Ordovician and Silurian as prominent faunal elements in the carbonate platform intertidal—shallow subtidal. Cruziana and related trace fossils, bivalves, and certain tribolites (notably homalonotids and dalmanitids) dominated most terrigenous platform intertidal—shallow subtidal faunas of the Ordovician and Silurian.Articulate brachiopods (primarily orthoids, strophomenoids, and rhynchonelloids) appear to have been relatively prominent during the Early Ordovician in shallow subtidal environments on both carbonate and terrigenous platforms and to have spread down the bathymetric gradient into increasingly deeper subtidal areas of both platforms during the latter part of the Ordovician. Tribolites dominated faunas in relatively moderate to deep subtidal environments on both platforms during the early part of the Ordovician. They were gradually replaced by brachiopods in first the shallower, and later the deeper subtidal as dominant members of the faunas. Brachiopods (primarily pentameroids and spiriferoids) dominated nearly all Silurian warm-water subtidal environments from the shallow subtidal to the edges of the platforms.Platform uplifts in the Middle Ordovician and glacio-eustatic sea-level fluctuations in the Late Ordovician caused environmental changes across the platforms that were accompanied by marked replacements among marine benthic faunas in all environments. The distribution of Ordovician carbonate platforms and glacial deposits suggests that an Ordovician polar region may have been close to present-day equatorial Africa and that Ordovician warm temperate-tropical regions lay close to the present-day North Pole.     

A modern-type Kimmeridgian reef (Ota Limestone,Portugal): Implications for Jurassic reef models

Upper Jurassic reefs rich in microbial crusts generally appear in deeper (sponge—‘algal’ crust reefs) or in very shallow but protected settings (coral or coral-coralline sponge meadows with ‘algal’ crusts). Upper Jurassic high-energy reefs (coral reefs and coral-stromatoporoid reefs) normally lack major participation of microbial crusts but rather represent huge bioclastic piles with only minor framestone patches preserved. An exception to this rule is represented by the high-energy, coral-‘algal’ Ota Reef from the Kimmeridgian of the Lusitanian Basin (Portugal). The narrow Ota Reef tract rims a small intra-basinal carbonate platform exhibiting perfect facies zonation (from W to E: Reef tract, back reef sands, peritidal belt, low-energy shallow lagoon). The reef is dominated by massive corals (Thamnasteria, Microsolena, Stylina). Complete preservation of coral framework is rare: like other Upper Jurassic high-energy reefs, the Ota Reef is very rich in debris; however, this debris is largely stabilized by algal and microbial crusts, what contrasts the other examples and gives the Ota Reef the appearance of a typical modern high-energy coral-melobesioid algal reef. Further similarities to modern reefs are the likely existence of a spur-and-groove system, the perfect sheltering of inner platform areas and the occurrence of small islands, as indicated by local blackenings and early vadose and karstic features.     

First report of Gogia (Eocrinoidea, Echinodermata) from the Early-Middle Cambrian of Sonora (Mexico), with biostratigraphical and palaeoecological comments

The blastozoan echinoderm genus Gogia is reported for the first time in the Early and the Middle Cambrian of Mexico. Reports in different members of the section of San José de Gracia (Sonora State, northwestern Mexico) extend the palaeogeographical range of the genus to the South Laurentia, and the stratigraphic range of Gogia granulosa to the whole first half of middle Middle Cambrian. Isolated plates occur in rocks deposited in detrital inner platform and complete specimens, in carbonate outer platform, confirming their ability to live in diverse environments. Their presence in these different environments through the Early-Middle Cambrian on Laurentia agrees with the onshore-offshore expansion of echinoderms during Cambrian.     

Paleoequatorial rain forest of western India during the EECO: evidence from Uvaria L. fossil and its geological distribution pattern

During the early Eocene, Rajasthan was positioned near the equator and had a warm and humid tropical climate dominated by tropical rainforests like the present-day equatorial forests of South India. Many of the plants retrieved as fossils from Rajasthan are growing there as refugee. This study further strengthens this view as it reports a new species of Uvaria L. from the early Eocene sediments of Bikaner (Rajasthan) showing its best resemblance with the extant U. zeylanica Deless. ex DC., which is presently growing in the evergreen forests of South India and Sri Lanka. The genus is thought to have originated in Africa, and the present finding gives an idea about its geologic distribution in Asia and Australasia via India relying on ‘stepping stone’ hypothesis during the Early Eocene Climatic Optimum (EECO) when climatic conditions were favourable for the luxuriant growth of tropical vegetation. A general cooling trend after EECO and change in the configuration of land and sea affected the climate on the regional scale causing total devastation of tropical evergreen forests that existed in western India during the depositional time; this change is ultimately responsible for creating dry and desertic conditions prevailing in the area at present.     

A nearshore–offshore trend in acritarch distribution from the Early–Middle Ordovician of the Yangtze Platform, South China

The stratigraphical interval of the late Early Ordovician Didymograptus deflexus and the early Middle Ordovician Azygograptus suecicus graptolite Biozones was investigated from seven sections from the upper Yangtze Platform, southern China. These are located on different parts of the platform, between the nearshore environments of the Kunming area, Yunnan Province, and the offshore carbonate shelf of the Yichang area, Hubei Province. The assemblages recovered from the different parts of the platform vary both in terms of diversity and composition. The nearshore environments show low diversity assemblages with about 10 acritarch species, whereas the offshore shelf environments reflect higher diversities with about 40 species. The composition of the assemblages also changes from simple morphologies (micrhystrids, leiosphaerids, fusiform acritarchs) in nearshore environments to specimens with longer and more complexly branched processes on the shelf. The polygonomorph acritarchs are common over all the upper Yantze Platform, while the acanthomorph genera Baltisphaeridium and Peteinosphaeridium are the most abundant taxa on the offshore carbonate shelf area. Phylogenetic or sea-level changes are probably not responsible for the compositional and diversity changes that occurred during the investigated interval. This study confirms previous interpretations that poorly diversified Palaeozoic acritarch assemblages occur in neritic environments and more complex, highly diversified assemblages are found on the shelf.     

The long‐term history of dispersal among lizards in the early Eocene: new evidence from a microvertebrate assemblage in the Bighorn Basin of Wyoming,USA

Abstract: Early Eocene mammal faunas of North America were transformed by intercontinental dispersal at the Paleocene–Eocene boundary, but lizard faunas from the earliest Eocene of the same area were dominated by immigrants from within the continent. A new lizard assemblage from the middle early Eocene of Wyoming sheds light on the longer‐term history of dispersal in relation to climate change. The assemblage consists of three iguanid species (including two new species possibly closely related to living Anolis), Scincoideus, ‘Palaeoxantusia’, four anguids, two species of an undescribed new anguimorph clade, Provaranosaurus and a varanoid (cf. Saniwa). Most North American glyptosaurin glyptosaurines are now referred to Glyptosaurus, and Glyptosaurus hillsi is given a new diagnosis. Scincoideus is otherwise known only from the mid‐Paleocene of Belgium, and the specimens described here are the first to document intercontinental dispersal to North America among lizards in the early Eocene. Like in mammals, some immigrant lizard lineages first appearing in the Bighorn Basin in the earliest Eocene persisted in the area long after the Paleocene–Eocene thermal maximum, but other immigrants appear to have been restricted to the Paleocene–Eocene thermal maximum.     

Depositional environments and facies development of the Cenomanian–Turonian Galala and Maghra el Hadida formations of the Southern Galala Plateau (Upper Cretaceous,Eastern Desert,Egypt)

The Cenomanian–Turonian (Upper Cretaceous) Galala and Maghra el Hadida formations of the Southern Galala Plateau in Wadi Araba (northern Eastern Desert, Egypt) represent marine depositional systems developing in response to the early Late Cretaceous transgression at the southern margin of the Neotethyan Ocean in tropical paleolatitudes. A facies analysis (litho-, bio- and microfacies) of these successions shows the presence of 22 facies types (FTs, six are related to the Galala Formation, while the Maghra el Hadida Formation is represented by 16 FTs). The Galala Formation was deposited in a fully marine lagoonal environment developing in response to a latest Middle to early Late Cenomanian transgression. The rich suspension- and deposit-feeding macrobenthos of the Galala Formation indicate meso- to eutrophic (i.e., green water) conditions. The facies types of the uppermost Cenomanian–Turonian Maghra el Hadida Formation suggest deposition on a homoclinal carbonate ramp with sub-environments ranging from deep-subtidal basin to intertidal back-ramp. Major and rapid shifts in depositional environments, related to (relative) sea-level changes, occurred in the mid-Late Cenomanian, the Early–Middle Turonian boundary interval, the middle part of the Middle Turonian and the Middle–Late Turonian boundary interval.     

Filling the North European Early/Middle Eocene (Ypresian/Lutetian) boundary gap: Insights from the Pyrenean continental to deep-marine record

The Early/Middle Eocene (Ypresian/Lutetian) transition is represented by a hiatus in many North European sections, including those in which the classic stratotypes were originally defined. However, the Global Stratotype Section and Point of the Lutetian Stage, which is still pending definition, should be placed at a globally correlatable event included within that unrepresented interval. The Pyrenean Eocene outcrops display sedimentary successions that offer the rare opportunity to analyse the Ypresian/Lutetian boundary interval in almost continuous sections and in very different settings. Seven reference stratigraphic sections were selected on the basis of their quality and correlated by means of biomagnetostratigraphic data. This correlation framework casts light on the sequence of chronostratigraphic events that characterize the Ypresian/Lutetian boundary interval, which may prove useful in defining the main correlation criterion of the base of the Lutetian.All of the Pyrenean sections show a similar sedimentary evolution, despite being up to 350 km apart from each other, containing deposits of different origins (intrabasinal carbonate sediments, siliciclastic sediments sourced from the Iberian plate, and terrigenous sediments sourced from the uplifting Pyrenees) and despite having been accumulated in different sedimentary environments (from continental to deep marine) and in different geodynamic settings (piggy-back basin, foreland basin and cratonic margin). This common evolution can be readily interpreted in terms of a sea-level driven depositional sequence whose lowstand and transgressive systems tracts are included within the Ypresian/Lutetian boundary interval. The Pyrenean Ypresian/Lutetian depositional sequence can reasonably be correlated with depositional sequences from classic North European areas, shedding light on the palaeoenvironmental history which in those areas has not been recorded. Furthermore, these depositional sequences may possibly correlate with others from the Antarctic Ocean and from New Jersey, as well as with oceanic temperature variations, suggesting that they might be the result of climatically-driven glacioeustatic sea-level changes. Should this hypothesis prove correct, it would confirm previous suggestions that the onset of Antarctic glaciations needs to be backshifted to the late Ypresian at least.     

Did the Late Paleocene thermal maximum affect the evolution of larger foraminifers? Evidence from calcareous plankton of the Campo Section (Pyrenees,Spain)

The larger foraminifer turnover (LFT), which marks the base of the Ilerdian stage, may be related to the Late Paleocene Thermal Maximum (LPTM), or be at least nearly coeval with that climatic event. Thus, the impact of the LPTM may have been greater than hitherto realised, having also affected mid-latitude shallow-marine biota. This conclusion has been reached after a re-study of the calcareous plankton of the uppermost Paleocene and lowermost Eocene interval of the Campo section in the central southern Pyrenees. Campo is an important reference section because it contains larger foraminifers, planktic foraminifers and calcareous nannofossils, and their co-occurrence was used to intercalibrate their respective zonal schemes. Previous studies at Campo placed the onset of planktic foraminiferal Zone P5 near the base of the Ilerdian, and the calcareous nannofossil NP9/NP10 chronal boundary (sensu Bybell, L.M., Self-Trail, J.M., 1995. Evolutionary, biostratigraphic and taxonomic study of calcareous nannofossils from a continuous Paleocene/Eocene boundary section in New Jersey. US Geol. Surv. Prof. Pap. 1554, pp. 1–36) not less than 150 m above the Ilerdian lower limit. By these estimates, the LPTM (known to have occurred in the middle part of Zone P5 and just before the NP9/NP10 boundary) would be an event much younger than the LFT.However, our reexamination of planktic foraminifers suggests that the base of the Ilerdian is probably situated at the middle of Zone P5 (a possibility proposed by Hillebrandt in 1965, but denied by later authors). For instance, Morozovella occlusa has been found for the first time in the Campo section. Its Last Appearance Datum (LAD), which in the Pyrenees was approximately coeval with that of Morozovella velascoensis (event used to place the top of Zone P5), has been identified in beds situated less than 70 m above the base of the Ilerdian. Such thickness represents a time span of a similar magnitude as the one which separated the LPTM and the LAD of M. occlusa in the deep-water hemipelagic succession of the Basque Basin, in the western Pyrenees. Autochthonous calcareous nannofossils are neither abundant nor well preserved in most of the studied interval, with Rhomboaster bramlettei (the marker of the base of Zone NP10) being extremely rare in lower and middle Ilerdian beds, a fact that makes it very difficult to fix the position of the NP9/NP10 boundary in the Campo section. However, the bases of zones NP9 and NP11 have been located, and they support the zonation with planktic foraminifers. These new data suggest that the LFT and the LPTM may have been coeval or nearly so, a possibility reinforced by correlation with sections of the Basque Basin.Specialists of larger benthic foraminifers can easily delineate the LFT in shallow water carbonate successions of the Tethys domain, and they propose to place the Paleocene/Eocene boundary at the base of the Ilerdian stage. On the other hand, the deep benthic extinction event (BEE) is a major global biotic turnover in the bathyal and abyssal realms, while the ∂13C excursion (CIE) is an excellent tool for correlation between marine and terrestrial records. Therefore, the synchrony or near synchrony postulated here between the LFT, BEE and CIE (all of them probably related to the LPTM) would argue strongly in favour of these events as the criterion to officially redefine the Paleocene/Eocene boundary.