The primate fossil record in the Iberian Peninsula

During the last decade, new discoveries in several Iberian basins, together with the description of previously unpublished finds, have significantly increased the recorded paleodiversity of fossil Primates (Mammalia: Euarchonta) in the Iberian Peninsula. Here we provide an updated compendium of the primate fossil record in Iberia during the Cenozoic and further summarize the changes in primate paleo­diversity through time, which are then analyzed in the light of changing climatic conditions. Thanks to favorable climatic conditions, the highest diversity of Iberian primates was reached during the Eocene, thus reflecting the radiation of both adapoids and omomyoids; only a single plesiadapiform genus is in contrast recorded in the Iberian Peninsula. Near the Eocene-Oligocene boundary, paleoclimatic changes led to a primate diversity crisis and other faunal changes, although two Iberian omomyoids survived the Grande Coupure. From the Middle Miocene onwards, catarrhine primates are recorded in the Iberian Peninsula. During the Middle and Late Miocene, they are represented by pliopithecoids and hominoids, restricted to NE Iberia. The Miocene hominoids from Iberia are of utmost significance for understanding the Eurasian hominoid radiation and its role in the origins of the great-ape-and-human clade. Following the local extinction of these taxa during the early Late Miocene, due to progressively increased seasonality and concomitant changes in plant communities, cercopithecoids are also recorded in the Iberian Peninsula from the latest Miocene through the Plio-Pleistocene, although they finally became locally extinct, whereas hominoids are again represented by fossil humans during the Pleistocene.Durante la última década, nuevos descubrimientos en varias cuencas ibéricas, junto con la descripción de hallazgos previos inéditos, han incrementado significativamente la paleodiversidad de Primates fósiles (Mammalia: Euarchonta) registrada en la Península Ibérica. Proporcionamos aquí un compendio actualizado del registro fósil de los primates en Iberia durante el Cenozoico, y resumimos además los cambios en paleodiversidad de los primates a lo largo del tiempo a la luz de las condiciones climáticas cambiantes. Gracias a condiciones climáticas favorables, la diversidad más alta de primates ibéricos se produjo durante el Eoceno, reflejando así la radiación tanto de los adapoideos como de los omomioideos; en cambio, sólo un único género de plesiadapiformes se registra en la Península Ibérica. Hacia el límite Eoceno-Oligoceno, los cambios paleoclimáticos condujeron a una crisis de diversidad de los primates y otros cambios faunísticos, aunque dos omomioideos ibéricos sobrevivieron a la Grande Coupure. Del Mioceno Medio en adelante, los primates catarrinos se registran en la Península Ibérica. Durante el Mioceno Medio y Superior, están representados por pliopitecoideos y hominoideos, restringidos al NE de Iberia. Los hominoideos del Mioceno de Iberia son de gran importancia para comprender la radiación de los hominoideos eurasiáticos y su papel en los orígenes del clado de los grandes antropomorfos y los humanos. A continuación de la extinción local de estos taxones du­rante el Mioceno Superior inicial, debido al incremento progresivo de la estacionalidad así como a cambios en las comunidades vegetales, los cercopitecoideos también se registran en la Península Ibérica a partir del Mioceno más terminal en adelante. Los cercopitecoideos se registran en la Península Ibérica durante todo el Plio-Pleistoceno, aunque finalmente también se extinguieron localmente, mientras que los hominoideos vuelven a estar representados otra vez por los humanos fósiles durante el Pleistoceno

Plio-Pleistocene climatic change had a major impact on the assembly and disassembly processes of Iberian rodent communities

Comprehension of changes in community composition through multiple spatio-temporal scales is a prime challenge in ecology and palaeobiology. However, assembly, structuring and disassembly of biotic metacommunities in deep-time is insufficiently known. To address this, we used the extensively sampled Iberian Plio-Pleistocene fossil record of rodent faunas as our model system to explore how global climatic events may alter metacommunity structure. Through factor analysis, we found five sets of genera, called faunal components, which co-vary in proportional diversity over time. These faunal components had different spatio-temporal distributions throughout the Plio-Pleistocene, resulting in non-random changes in species assemblages, particularly in response to the development of the Pleistocene glaciations. Three successive metacommunities with distinctive taxonomic structures were identified as a consequence of the differential responses of their members to global climatic change: (1) Ruscinian subtropical faunas (5.3–3.4 Ma) dominated by a faunal component that can be considered as a Miocene legacy; (2) transition faunas during the Villafranchian–Biharian (3.4–0.8 Ma) with a mixture of different faunal components; and (3) final dominance of the temperate Toringian faunas (0.8–0.01 Ma) that would lead to the modern Iberian assemblage. The influence of the cooling global temperature drove the reorganisation of these rodent metacommunities. Selective extinction processes due to this large-scale environmental disturbance progressively eliminated the subtropical specialist species from the early Pliocene metacommunity. This disassembly process was accompanied by the organisation of a diversified metacommunity with an increased importance of biome generalist species, and finally followed by the assembly during the middle–late Pleistocene of a new set of species specialised in the novel environments developed as a consequence of the glaciations

Cricetidae and Gliridae (Rodentia, Mammalia) from the Miocene and Pliocene of southern Spain

Several Miocene and Pliocene continental fossiliferous localities in the Granada and Guadix basins have yielded fossil micromammals. Cricetids and glirids are known from most of these localities. This paper deals with the genera Apocricetus, Ruscinomys, Blancomys and Eliomys. The Cricetidae are important biostratigraphical markers, especially Apocricetus. The presence of A. barrierei in the locality PUR-4 indicates the beginning of the Early Ruscinian. The continuous record of Ruscinomys during the Late Turolian and the Early Ruscinian corroborates the lineage between R. schaubi and R. lasallei. The occurrence of a large specimen of Blancomys in the Granada Basin seems to indicate two phylogenetic lineages during the Late Turolian. The studied specimens of Eliomys allow us to confirm the relationship between E. intermedius and E. quercinus

Cricetidae and Gliridae (Rodentia, Mammalia) from the Miocene and Pliocene of southern Spain

Several Miocene and Pliocene continental fossiliferous localities in the Granada and Guadix basins have yielded fossil micromammals. Cricetids and glirids are known from most of these localities. This paper deals with the genera Apocricetus, Ruscinomys, Blancomys and Eliomys. The Cricetidae are important biostratigraphical markers, especially Apocricetus. The presence of A. barrierei in the locality PUR-4 indicates the beginning of the Early Ruscinian. The continuous record of Ruscinomys during the Late Turolian and the Early Ruscinian corroborates the lineage between R. schaubi and R. lasallei. The occurrence of a large specimen of Blancomys in the Granada Basin seems to indicate two phylogenetic lineages during the Late Turolian. The studied specimens of Eliomys allow us to confirm the relationship between E. intermedius and E. quercinus

Dating the change from endorheic to exorheic conditions in the drainage system of the Granada Basin (southern Spain)

The drainage system of the Granada Basin in southern Spain has evolved from endorheic to exorheic since the basin emerged and became continental in the latest Tortonian (late Miocene). The age of implementation for the recent exorheic, east-west drainage can now be identified by small mammal dating. This drainage configuration began in the latest Pliocene–earliest Pleistocene due to the capture of the Genil River by a Cacín River tributary. It represented an important change in the behavior of the basin and therefore in the geomorphology, as depositional forms and processes were replaced by erosive ones. While the basin was endorheic, sedimentation was active throughout the basin. Afterward the change to exorheic and up to the present, erosion dominates and sedimentation occurs only in some small, fault-controlled depositional depocenters