“Earliest Zanclean age for the Colombacci and uppermost Di Tetto formations of the « latest Messinian » northern Apennines: New palaeoenvironmental data from the Maccarone section (Marche Province, Italy)” by Popescu et al. (2007) Geobios 40 (359-373)

Two possible alternative interpretations of the claimed Zanclean age (Popescu et al., 2007) of two historical lithostratigraphic units of the Northern Apennines, usually referred to as Late Messinian in age and recording the so called Lagomare final event of the Messinian salinity crisis (MSC), are here discussed. The wrong age attribution of the Colombacci and “tetto” Fms. is ruled out based on data from the Maccarone and other sections showing that the Colombacci-Argille Azzurre Fm. boundary is basin wide synchronous and coincident with the Miocene-Pliocene boundary as far as it has been formally defined in the Eraclea Minoa GSSP. Alternatively, the opportunity of emending the Zanclean GSSP to a stratigraphically lower horizon recording the first evidence of marine influences in the Mediterranean following the MSC peak, seems not suitable, as (1) the marine signature of uppermost Messinian deposits is weak and still controversial and (2) no significant bio- and magnetostratigraphic events, well chronologically defined and recognizable at a global scale appear to be available to such a purpose.     

Pliocene Atlantic molluscan assemblages from the Mondego Basin (Portugal): Age and palaeoceanographic implications

The Pliocene molluscan assemblage from the Mondego Basin (Portugal, Western Iberia) plays a particularly important role in the understanding of the palaeobiogeography of Neogene–Quaternary molluscs of the Atlantic Frontage of Europe and the western Mediterranean. The importance of these Portuguese molluscan deposits is stressed, as it is the only assemblage representative of the southern portion of the Pliocene French–Iberian biogeographical Province.The Pliocene marine fossiliferous deposits of the Mondego Basin (central-west Portugal) are dated using their nannofossil and molluscan assemblages, as well as Strontium dating. The results suggest a late Zanclean to early Piacenzian age. Chronologically they are equivalent to the Mediterranean Pliocene Molluscan Unit 1 (MPMU1). However, due to the more northern geographical location of the Mondego Basin assemblages, their molluscan content is closer to that of MPMU2 than to that of MPMU1 in the Mediterranean.The presence of a stock of thermophilic taxa in the Mondego assemblage, no longer existent in European waters, enabled us to suggest a palaeoenvironmental reconstruction for mid-Pliocene SSTs in the region. We put forward the hypothesis that the SSTs at the latitude of Mondego, during late Zanclean to early Piacenzian, would be characterized by a yearly SST pattern analogous to that of present-day Cape Blanc (West Africa). Consequently, whilst subtropical conditions existed in the Atlantic Zanclean to mid-Piacenzian at Mondego latitude in the Mediterranean fully tropical conditions prevailed at that time. The Mondego SST estimates correlate with those estimated for MPMU2 in the Mediterranean.The global palaeoenvironmental reconstruction of mid-Pliocene SSTs in the PRISM2 Project suggests, for western Iberia, at Mondego latitude, an August SST of about 23 °C, and a February temperature of about 17 to 18 °C. Our hypothesis suggests similar August SST differing in only half a degree Celsius (23.5 vs. 23 °C) and February SSTs slightly higher (19 vs. 17–18 °C).     

Messinian‐Zanclean vegetation and climate in North‐Central Italy

A palynological study was carried out on four Italian Miocene‐Pliocene sections ranging in age from uppermost Tortonian to Zanclean located on the Adriatic side of the North‐Central Apennines. The study documents the Mediterranean isolation, the salinity crisis (s.s), the “lago‐mare”; event and the re‐establishment of open‐marine conditions in the Mediterranean at the beginning of the Pliocene. From a climatic point of view, a transition from subtropical/warm‐temperate conditions during the Messinian to warm‐temperate/temperate conditions during the Zanclean is recorded. The presence of a lower thermic level, with respect to the Messinian, the re‐establishment of open‐marine conditions and the uplift of the Apennines were major factors controlling paleoenvironmental variations during the Zanclean. The latter is also characterized by cyclic temperature oscillations. Correlations with coeval sections in the Mediterranean area confirm the existence of latitudinal climatic gradients within the studied area.     

Latest Messinian “Lago-Mare” Lymnocardiinae from Italy: Close relations with the Pontian fauna from the Dacic Basin

Rich hypo- to mesohaline molluscan assemblages characterising the latest Messinian “Lago-Mare” biofacies, composed of prosobranch gastropods (Neritidae, Thiaridae, Melanopsidae, Hydrobiidae) and bivalves of the families Cardiidae (subfamily Lymnocardiinae) and Dreissenidae, are widespread in shallow water basins characterized by low salinities within the Mediterranean realm, during the post-evaporitic phase in the time-span 5.5-5.3 Ma. Several genera and species are recorded in the Italian uppermost Messinian sediments. While the gastropods show endemic character being linked to continental water-systems, Lymnocardiinae and Dreissenidae have strong Paratethyan affinity. New records of significant species of Lymnocardiinae from the uppermost Messinian sediments of Tuscany, Marches and Sicily and the systematic review of the old literature data point out close relations of the Italian fauna with that from the Pontian sediments of the Dacic Basin. The palaeobiogeographical data referred to Messinian and Pontian Lymnocardiinae suggest that the Aegean Basin could be an intermediate basin from whence the Pontian Paratethyan-type fauna migrated into the Mediterranean area during the latest Messinian. Since the ecology of Lymnocardiinae is mainly tied to oligo- and mesohaline water, spreading of suitable habitats in depositional systems of marginal settings characterized by increasing freshwater influx after the “salinity crisis” favoured their dispersal into the Mediterranean area from the Paratethys realm.     

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.     

Paleoenvironmental evolution of the eastern Mediterranean during the Messinian: Constraints from integrated microfossil data of the Pissouri Basin (Cyprus)

Integrated data of calcareous nannofossils, as well as planktonic and benthic foraminifera from the Pissouri Motorway section on Cyprus allow the reconstruction of surface- and bottom-water paleoenvironments of the eastern Mediterranean during the interval preceding the Messinian salinity crisis (MSC). Contrary to deeper-water locations, where benthic foraminifera faunas are suppressed or absent just after the Tortonian–Messinian boundary, sediments deposited at intermediate water depths do contain benthic assemblages. From the earliest Messinian onwards, a development towards increasingly unfavourable paleoenvironments is reflected in the planktonic and benthic microfossil records of the Pissouri section and proceeds with rather discrete time steps that can be correlated to sequences throughout the Mediterranean. Shortly after the Tortonian–Messinian boundary a transition is recorded in the sedimentology and the open marine, deeper-water taxa disappear from the benthic foraminifera assemblages; subsequently, the diversity of all fauna groups diminishes. The changes recorded at species level in both surface-water and sea-floor dwelling taxa suggest decreasing circulation of the bottom waters, associated with changes in the surface waters, most likely due to increasing stratification. From ∼6.73 Ma onwards, our data indicate a prominent change to more restricted conditions and increasing salinity at the sea floor together with intermittently rising surface water salinity. The dominance of oligotypic and monospecific assemblages and the frequent shifts in assemblage compositions of all microfossil groups indicate severely stressed environments after ∼6.4 Ma, probably related to increased salinity. The major changes in paleoenvironmental conditions, including oxygen deprivation due to stagnation and hypersalinity, can be explained by hydrographical changes in the Mediterranean basin, which are probably caused by tectonic movements in the Rif Corridor acting in concert with astronomical cyclicity. Evaluation of the paleodepth proxies indicates that the depth of the Pissouri Basin remained rather constant at ∼300–500 m, with a minimum of 200 m, until deposition of the “barre jaune”, the transitional interval towards the evaporites and that early shallowing to neritic depths, as was proposed before, is highly unlikely.     

The late Messinian Lago-Mare episode in the Mediterranean Basin: Preliminary report on the occurrence of Paratethyan ostracod fauna from central Crete (Greece)

In the Crete Island, late Messinian Lago-Mare facies are not well known. At present, the occurrence in Crete of the uppermost Messinian post evaporitic deposits is a matter of debate. According to several authors, the well-known late Messinian Lago-Mare facies does not occur in Crete. In this paper the preliminary results obtained from the biostratigraphical analysis of some sections sampled in the Messarà Plain will be shown. Nearby Faneromeni and Ano Akria villages, the Miocene/Pliocene boundary is well exposed. There, gypsum-bearing clay, laminated microcrystalline gypsum and gypsum-rudites characterize the evaporitic deposits of the Messinian stage. In these areas, above the Messinian evaporite, post-evaporitic fine-laminated polychrome clays, with intercalations of sandstones and conglomerates, have been found. In both the Faneromeni and Ano Akria area, the Pliocene grey clays and conglomerates rest unconformably on the uppermost Messinian post-evaporitic deposits. A 20 cm-spaced sampling has been performed in both the sections, for more than 100 samples collected. The results of the micropaleontological analysis performed on the Faneromeni and Ano Akria sections point to the occurrence of ostracod assemblages containing: Loxocauda limata (Schneider in Agalarova et al.), Loxocauda sp., Cytherura pyrama Schneider, Cyprideis anlavauxensis Carbonnel, Cyprideis agrigentina Decima, Amnicythere palimpsesta (Livental), Amnicythere propinqua (Livental), Amnicythere accicularia (Olteanu), Amnicythere costata (Olteanu), Amnicythere multituberculata (Livental), Amnicythere sp. D (Miculan in Bassetti et al.), Amnicythere sp. 2 Gliozzi and Grossi, Amnicythere sp., Euxinocythere (Maeotocythere) praebaquana (Livental in Agalarova et al.), Mediocytherideini indet., Pontoniella pontica (Agalarova), Camptocypria sp. 1 Gliozzi and Grossi, Caspiocypris sp., Zalanyiella venusta (Zalanyi), Tyrrhenocythere sp., Loxoconcha rhombovalis Pokorny, Loxoconcha eichwaldi Livental, Loxoconcha sp. A (Miculan in Bassetti et al.), Loxocorniculina djafarovi (Schneider in Suzin). In the analysed samples, reworked planktonic foraminifers and well-preserved charophyte gyrogonites have been also found. The ostracod assemblages found in the Messarà Plain belong to the Loxocorniculina djafarovi Zone (sensu Carbonnel, 1978), which characterizes the uppermost Messinian deposits of the whole Mediterranean Basin. At that time, the well-known Lago-Mare biofacies was also widespread on the Crete Island. The presence of Paratethyan ostracods in the post-evaporitic Messinian deposits of both Faneromeni and Ano Akria sections suggests that in the Crete Island the latest Messinian sedimentation took place in brackish water palaeoenvironments.     

Did the Mediterranean marine reflooding precede the Mio–Pliocene boundary? Paleontological and geochemical evidence from upper Messinian sequences of Tuscany,Italy

The events related to the Messinian salinity crisis are among the most deeply investigated of Earth's history. According to the current hypothesis of Neogene paleogeographic evolution, approximately 5.5 Ma ago, after evaporitic sedimentation and before the Mio–Pliocene boundary, the Mediterranean was characterized by the widespread development of non-marine environments inhabited by molluscs and ostracods of brackish affinity. The Messinian post-evaporitic deposits that testify such a dramatic environmental change are commonly referred to as ‘Lago-mare’ and have been reported from several outcrops and boreholes throughout the entire Mediterranean basin. The origin of ‘Lago-mare’ conditions is commonly interpreted as the result of the synergistic effect of both the humid climatic conditions and change of the drainage patterns at the Mediterranean scale, with the capture of Paratethyan brackish waters. A few recent studies, however, suggest that such a scenario probably represents an oversimplification of the original context, from both a paleogeographical and paleoenvironmental point of view. Unfortunately, the results of these studies have never been commonly accepted and the proposed evidences have been considered questionable. In this paper we describe the fish assemblages from the ‘Lago-mare’ deposits of two localities, Cava Serredi and Podere Torricella, located in the Neogene hinterland basins of Tuscany, central Italy. These assemblages consists of a mixture of marine euryhaline and stenohaline taxa suggesting that the depositional environments were characterized by permanently open connections with a marine basin filled with normal marine waters. In order to better define the paleontological significance of these upper Messinian fish assemblages, the oxygen, carbon and strontium isotopic composition of fish otoliths and other fossils has been measured. These isotopic compositions are strongly indicative of the presence of normal marine conditions close to the depositional environments testified by the sedimentary sequences, thereby implying that the interpretation of the geochemical results are consistent with those derived from the paleoecological analyses of the fish assemblages. Based on the integrated paleoichthyological–geochemical approach discussed in this paper it is possible to unambiguously demonstrate that normal marine rather than fresh- or brackish waters were present in the Mediterranean at least during the upper part of the ‘Lago-mare’ event, providing an unquestionable evidence that the marine refilling of the basin preceded the Mio–Pliocene boundary.     

Origines du peuplement mammalien en Afrique du Nord durant le miocène terminal

The late Miocene North African mammalianassemblage is considered here from three viewpoints: survivals, extinctions, and immigrations. The Eurasiatic affinities of the large mammals slightly prevail over the Ethiopian affinities. Amongst the North African large mammals, 4 to 8 taxa are Eurasiatic immigrants, while 4 to 6 are of Subsaharian origin. Contrarily, the micromammalian fauna is highly endemic, with only one species, a murid (Paraethomys miocaenicus), considered here as being related to an Asiatic form (Karnimata darwini). Our study of Eurasian and African Miocene faunas reveals that during the late Astaracian-early Turolian interval, the Saharo-Arabic belt permitted very little latitudinal faunal exchanges. However, during the middle and late Turolian such faunal exchanges became frequent. The micromammal record unequivocally indicates that a brief period of faunal exchange occurred between Africa and western Europe at the end of the Miocene, corresponding with the Messinian Salinity Crisis. The increased intercontinental faunal exchange between Africa and Eurasia during the late Miocene coincides with, and counterbalances the extinction of more than 10 taxa at the Mio/Pliocene boundary.     

Histoire plio-pléistocène des écosystèmes végétaux de Méditerranée sud-occidentale : apport de l’analyse pollinique de deux sondages en mer d’Alboran

The pollen analysis of sediments of two boreholes located in the northeastern Morocco (Nador 1) and in the southeastern Spain (Andalucia G1) has allowed shedding a new light on the vegetation and climate of the North African littoral plains, the Rif Massif and the Betic Range during the Pliocene. The vegetation around the Alboran Sea was open and xeric during the Zanclean, dominated by herbs including subdesertic elements as Calligonum, Lygeum, Nitraria and Neurada. This type of vegetation indicates a dry and hot climate. The southwestern Mediterranean steppes have therefore a climatic character; they existed before the presence and the heavy pressure of Man on the environment. From the Piacenzian, the development, at Andalucia as well as at Nador, of Artemisia and the appearance of some altitude trees such as Cedrus and Cathaya indicate a vegetation change linked to a climatic change. Modifications in the vegetation observed during the same period in northwestern Mediterranean seem to indicate that the vegetation changes observed at Andalucia and Nador are controlled by the appearance of the first arctic glacial-interglacial cycles. The cedar tree appears at Nador only at the end of the Piacenzian, at time of the first cooling, while it has been found punctually in Messinian and early Pliocene sediments of Habibas in Algeria and in Messinian sediments of the Bou Regreg section at Salé in Morocco. The regular presence of Cedar at Bou Regreg during the Messinian, allows supposing that it was present in the Middle Atlas Mountains and that its development was favoured by colder conditions.     

Geological setting of Pliocene rifting and deposition in the Afar Depression of Ethiopia

Tectonic extension of the Afar amounts to 10–30 km since 1–2 Ma and to 40–60 km since 3–5 Ma ago, or rougly 1–2 cm per year. Active faulting, volcanism, and development of the Pliocene and younger Afar grabens with their rich hominid and other vertebratefaunas, have been controlled by ENE and WNW oriented lineaments or ancient zones of structural weakness. These lineaments also controlled the alignment of the Gulf of Aden and Red Sea, respectively.Crustal stresses resulting from the late Miocene (Messinian) salinity crisis in the Mediterranean basin may have triggered renewed tectonic movements along certain pre-existing lineaments such as the Levant Shear. Separation of Africa from Arabia (and hence the inception of Afar) was controlled by tectonic events far removed from NE Africa, including possible Miocene fusion of the Indo-Arabian plates.During the early Pliocene, the Ethiopian uplands were far lower (possibly by 1000 m) and the southern Afar-Middle Awash region was higher, so that topographic and climatic contrasts between plain and plateau were less pronounced and the Afar climate was less arid than today.There was a major change from lacustrine to fluviatile deposition in the Middle Awash valley soon after 4·0–3·8 Ma ago, caused by extensional tectonics. Within the topographic constraints imposed by volcano-tectonic activity, regional climatic oscillations have controlled the detailed pattern of Pliocene (and later) sedimentation in Afar.     

Pleistocene fish otoliths from the Mediterranean Basin: a synthesis

An overview of upper pPliocene and pleistocene otolith assemblages is compiled on the basis of both literature data and newly collected material from several sections located mainly in southern Italy. One hundred and five taxa are listed. Additional comments are provided for taxa subject to discussion. The composition and affinities of the Mediterranean Pleistocene otolith associations (consisting mainly of deep sea fishes) is checked against the available data for Pre-Messinian, Pliocene, and Recent Mediterranean fishes. This analysis is based on the recorded nominal species, but some taxa that could be identified at the generic level only are also included when they are relevant from a biogeographic point of view. Some new data on Piacenzian (middle Pliocene) and Gelasian (upper Pliocene) otoliths are also provided because this time interval still constitutes a major gap in the knowledge of the stratigraphic range of Plio-Pleistocene fish taxa. The Pleistocene deepwater fish fauna of the Mediterranean shows a markedly more oceanic character than the present-day one, a tendency that was all ready observed from early Oligocene till Pliocene times. Starting from the late Piacenzian, an increasing number of Atlantic taxa progressively invaded the Mediterranean including several subpolar and temperate forms. This invasion became stronger in the Gelasian. From this period up to the middle and late Pleistocene, the Mediterranean deepwater fish fauna (mesopelagic and benthopelagic) is enriched by taxa which today are typical for the north Atlantic cold deep water. This faunal shift seems to be correlated with the evolution of the Plio-Pleistocene Mediterranean paleoceanographic setting as well as with the global climatic deterioration.     

Neogene history of Sporolithon Heydrich (Corallinales,Rhodophyta) in the Mediterranean region

Most modern species of Sporolithon live in tropical and subtropical areas and only one species of the genus, S. ptychoides, occurs in the Mediterranean Sea. The scarce present-day populations of Sporolithon in the Mediterranean region are relics of a long history of the genus in this area since the Early Cretaceous. Analysis of data from the palaeontological literature, combined with the study of both fossil samples and Recent ones collected from Italy and Spain, shows that during the Miocene variations in the number of Sporolithon species in the Mediterranean region parallel changes in global temperature. After a maximum species richness in the Langhian (early Mid Miocene), coincident with the Miocene climatic optimum, the number of species decreased to just two before the Messinian Salinity Crisis. This marked decline follows the global cooling event that began at around 14 Ma. The closure of the connections of the Mediterranean region with the Indian Ocean during the Langhian left Mediterranean Sporolithon populations isolated from the main dispersal area of the genus. After the Messinian desiccation, a single species, S. ptychoides, re-invaded the Mediterranean Basin during the Early Pliocene and continues to inhabit this temperate sea today. The Atlantic Ocean is the most probable source of the re-invading Sporolithon plants.     

Fluvial basin history in the northeastern Mediterranean region underlies dispersal and speciation patterns in the genus Dugesia (Platyhelminthes,Tricladida, Dugesiidae)

In this study we analyzed the phylogenetic relationships of eastern Mediterranean freshwater planarians of the genus Dugesia, estimated divergence times for the various clades, and correlated their phylogeographic patterns with geological and paleoclimatic events, in order to discover which evolutionary processes have shaped the present-day distribution of these animals. Specimens were collected from freshwater courses and lakes in continental and insular Greece. Genetic divergences and phylogenetic relationships were inferred by using the mitochondrial gene subunit I of cytochrome oxidase (COI) and the nuclear ribosomal internal transcribed spacer-1 (ITS-1) from 74 newly collected individuals from Greece. Divergence time estimates were obtained under a Bayesian framework, using the COI sequences. Two alternative geological dates for the isolation of Crete from the mainland were tested as calibration points. A clear phylogeographic pattern was present for Dugesia lineages in the Eastern Mediterranean. Morphological data, combined with information on genetic divergences, revealed that eight out of the nine known species were represented in the samples, while additional new, and still undescribed species were detected. Divergence time analyses suggested that Dugesia species became isolated in Crete after the first geological isolation of the island, and that their present distribution in the Eastern Mediterranean has been shaped mainly by vicariant events but also by dispersal. During the Messinian salinity crisis these freshwater planarians apparently were not able to cross the sea barrier between Crete and the mainland, while they probably did disperse between islands in the Aegean Sea. Their dependence on freshwater to survive suggests the presence of contiguous freshwater bodies in those regions. Our results also suggest a major extinction of freshwater planarians on the Peloponnese at the end of the Pliocene, while about 2 Mya ago, when the current Mediterranean climate was established, these Peloponnese populations probably began to disperse again. At the end of the Pliocene or during the Pleistocene, mainland populations of Dugesia colonized the western coast, including the Ionian Islands, which were then part of the continent.     

Pleistocene extinctions as drivers of biogeographical patterns on the easternmost Canary Islands

Subtropical islands are often viewed as refuges where Quaternary climatic shifts driving global episodes of extinction were buffered. Island biodiversity, however, may have been impacted by climatic fluctuations at local scales, particularly in spatially heterogeneous island systems. In this study, we generated a conceptual framework for predicting the potential impact of Pleistocene extinctions on the biogeographical pattern of the Canarian spermatophyte flora, with a focus on the easternmost Canarian islands (ECI). Then, we performed an exhaustive bibliographic revision (270 studies) to examine whether taxonomic, phylogenetic and phylogeographical data support our predictions. Although molecular information is limited for many lineages, the available data suggest that the majority of extant ECI plant taxa may be the result of relatively recent (<1 Ma) dispersal from surrounding insular and mainland areas. Different lines of evidence are compatible with the idea of a Pleistocene period of frequent lineage extirpation on ECI. Extinction may thus have provided new ecological opportunities for recent (re)colonization, with some cases of recent establishment mediated by facilitation. Considering background extinction on ECI, we describe five general patterns of colonization for Canarian plant lineages. In addition to factors related to island ontogeny and long‐distance dispersal, we suggest that Pleistocene extinctions may have significantly contributed to extant biogeographical patterns in the Canarian archipelago, such as the biased distribution ranges of island plants and the low endemic richness on ECI. This new scenario provides testable hypotheses for future studies dealing with the phylogeography, taxonomy and conservation of terrestrial biodiversity on the Canarian islands, and possibly, on other near‐shore islands.     

Climatic inference from the history of the taxodiaceae during the pliocene and the early pleistocene in Western Europe

The Taxodiaceae are present throughout Western Europe during the Early Pliocene. Chronological data show that their extinction begins during the Middle Pliocene in the French Mediterranean area and that it occurs later (during the Late Pliocene and Early Pleistocene) in northwestern Europe, in elevated regions and in Italy. This chronology is difficult to understand if we accept cooling of the climate as the only determining factor of this extinction. The non-synchronous extinction of the Taxodiaceae in Western Europe reflects the more complex pattern of climatic phenomena which include variations in precipitation and temperature at different times and with differing intensity according the area. A decrease in precipitation forced the extinction of the Taxodiaceae in southeastern France (summer drought) and it occurred before the temperature threshold for Taxodiaceae was reached in the other parts of Europe.     

Late Miocene biota from the Abad Member of the Carboneras-Nijar Basin (Spain,Andalusia): A bathyal fossil assemblage pre-dating the Messinian salinity crisis

Marly sediments of the early Messinian Abad Member of the Turre Formation from the northeastern sector of the Carboneras-Nijar Basin (southern Spain) have yielded a rich fossil assemblage, of which 60 taxa are documented herein. Besides nannoflora and microfauna, this assemblage includes the first autochthonous macrofauna described from the Abad Member. Based on the calcareous nannofossil assemblage, in particular the occurrence of the zonal index taxon Amaurolithus primus, the sediments are assigned to the Mediterranean calcareous nannofossil zone CNM17, corresponding to the latest Tortonian to earliest Messinian interval. This matches the age range generally reported for the Abad Member. Palaeoecological evidence from calcareous nannofossils (20 autochthonous taxa), planktic and benthic foraminifera (12 taxa), Porifera (3 taxa), Octocorallia (Keratoisis), Serpulidae (4 taxa), Bivalvia (5 taxa), Gastropoda (2 taxa), Brachiopoda (7 taxa), Cirripedia (Faxelepas) and Vertebrata (5 taxa) indicates an upper bathyal environment with an influx of neritic elements for the Abad Member near Carboneras. Additionally, several faunal components may represent allochthonous/parautochthonous elements from adjacent habitats, which were transported into the deep marine setting by turbiditic mass flows. Although similarities exist, the fossil assemblage from the marls is compositionally significantly different from the biota previously documented from a nearby exposed olistostrome, the ‘red breccia’. Similar fossil assemblages from the Mediterranean have so far mainly been reported from the Pliocene-Pleistocene of southern Italy and Greece. The Carboneras fauna thus adds to our knowledge of the development of these habitats and their biota prior to the Messinian salinity crisis. Beyond the novel palaeoenvironmental data, the range of the dyscoliid brachiopod Ceramisia meneghiniana, previously known only from the Pliocene of Italy, is extended to the Miocene of Spain. The cirripede crustacean Pycnolepas paronai De Alessandri, 1895 is transferred to the hitherto monospecific genus Faxelepas Gale, 2015, whereby the range of the latter (previously Maastrichtian to Danian) is extended to the late Miocene.     

Miocene to Pliocene vegetation reconstruction and climate estimates in the Iberian Peninsula from pollen data

Pollen analysis of Miocene and Pliocene sediments from the Iberian Peninsula shows a progressive reduction in plant diversity through time caused by the disappearance of thermophilous and high-water requirement plants. In addition, an increase in warm-temperate (mesothermic), seasonal-adapted “Mediterranean” taxa, high-elevation conifers and herbs (mainly Artemisia) occurred during the Middle and Late Miocene and Pliocene. This has mainly been interpreted as a response of the vegetation to global and regional processes, including climate cooling related to the development of the East Antarctic Ice Sheet and then the onset of the Arctic Ice Sheet, uplift of regional mountains related to the Alpine uplift and the progressive movement of Eurasia towards northern latitudes as a result of the northwards subduction of Africa. The development of steppe-like vegetation in southern Iberia is ancient and probably started during the Oligocene. The onset of a contrasted seasonality in temperature during the Mid-Pliocene superimposed on the pre-existing seasonality in precipitation, the annual length of which increased southward. The Mediterranean climatic rhythm (summer drought) began about 3.4 Ma and caused the individualization of modern Mediterranean ecosystems. Quaternary-type Mediterranean climatic fluctuations started at 2.6 Ma (Gelasian) resulting in repeated steppe vs. forest alternations. A latitudinal climatic gradient between the southern and the northern parts of the Iberian Peninsula existed since the Middle Miocene.     

Phylogenetic Clustering of Origination and Extinction across the Late Ordovician Mass Extinction

Mass extinctions can have dramatic effects on the trajectory of life, but in some cases the effects can be relatively small even when extinction rates are high. For example, the Late Ordovician mass extinction is the second most severe in terms of the proportion of genera eliminated, yet is noted for the lack of ecological consequences and shifts in clade dominance. By comparison, the end-Cretaceous mass extinction was less severe but eliminated several major clades while some rare surviving clades diversified in the Paleogene. This disconnect may be better understood by incorporating the phylogenetic relatedness of taxa into studies of mass extinctions, as the factors driving extinction and recovery are thought to be phylogenetically conserved and should therefore promote both origination and extinction of closely related taxa. Here, we test whether there was phylogenetic selectivity in extinction and origination using brachiopod genera from the Middle Ordovician through the Devonian. Using an index of taxonomic clustering (R_CL) as a proxy for phylogenetic clustering, we find that A) both extinctions and originations shift from taxonomically random or weakly clustered within families in the Ordovician to strongly clustered in the Silurian and Devonian, beginning with the recovery following the Late Ordovician mass extinction, and B) the Late Ordovician mass extinction was itself only weakly clustered. Both results stand in stark contrast to Cretaceous-Cenozoic bivalves, which showed significant levels of taxonomic clustering of extinctions in the Cretaceous, including strong clustering in the mass extinction, but taxonomically random extinctions in the Cenozoic. The contrasting patterns between the Late Ordovician and end-Cretaceous events suggest a complex relationship between the phylogenetic selectivity of mass extinctions and the long-term phylogenetic signal in origination and extinction patterns.     

Calcareous nannofossils and foraminifers herald the Messinian Salinity Crisis: The Pollenzo section (Alba, Cuneo; NW Italy)

During the Messinian, the Mediterranean area experienced fast and prominent paleoenvironmental changes, culminating in the so-called Messinian Salinity Crisis, with the deposition of the evaporitic series. This work investigates the micropaleontological assemblages in the pre-evaporitic sediments of the Sant’Agata Fossili Marls (SAF) of the Pollenzo section (Cuneo area, North Western Italy). A semiquantitative analysis is carried out on the upper part of the marly and pelitic sediments of the SAF underlying the first gypsum bed, ascribed to the Vena del Gesso Fm. (VDF). The studied interval belongs to the planktonic foraminifer Globorotalia conomiozea Zone and “non distinctive Zone” of Iaccarino and to the calcareous nannofossil MNN11b/c Zone of Raffi et al. (1998, 2003) ( [Raffi et al., 1998] and [Raffi et al., 2003]). Decrease of diversity and abundance of the foraminifer and calcareous nannofossil assemblages is recorded 12 m below the VDG and clearly reflects environmental stress. From bottom to top, six paleoecological events are recorded: (1) the first peak abundance of “small” Reticulofenestra and the last recovery (LR) of planktonic foraminifers; (2) the peak abundance of Pontosphaera japonica and the last recovery of warm water taxa Discoaster spp.; (3) the last recovery of benthic foraminifers; (4) the co-occurring peak abundances of Helicosphaera carteri and Sphenolithus abies, and the last recovery of warm water taxa Amaurolithus spp.; (5) the second peak of “small” Reticulofenestra; (6) the definitive disappearance of calcareous nannofossils. These paleoecological events describe a progressive isolation of the basin from the world ocean and increasingly stressed environment (LR planktonic foraminifers; LR Discoaster spp.), increasing dysoxic to anoxic conditions at the sea floor (LR benthic foraminifers), shallowing of the water column (peak of H. carteri), increasing salinity in surface waters (peak of S. abies), and enhanced nutrient concentration in surface waters (peak of “small” Reticulofenestra); these are related to paleoenvironmental changes predating gypsum deposition at Pollenzo and affecting the whole Mediterranean basin.