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Tanto los machos como muchas de las hembras del ciervo primitivo Dicrocerus elegans de Sansan (Mioceno Medio, Francia) poseían apéndices craneales de tipo asta que consisten en una protoasta bifurcada y ornamentada con surcos y crestas que es sustentada por un pedículo moderadamente largo. La capacidad de la protoasta de ser expulsada y regenerada es evidente a partir de los ejemplares de desmogue y también por las diferencias histológicas existentes entre la protoasta y el pedículo. El primer apéndice consiste en una vara larga, comprimida lateralmente, y con el ápice bifurcado, sin que se observe ningun límite apreciable entre la protoasta y el pedículo. En las hembras, el ángulo que forman los margenes anterior y posterior del apéndice es más agudo que en los machos (los márgenes son más paralelos en vista lateral). Tras el primer desmogue, la base de la protoasta es más amplia que la sección distal del pedículo, y se desarrolla una estructura similar a la roseta en la parte medial. Con los sucesivos desmogues, el pedículo se acorta y su sección se hace más circular, mientras que la protoasta es cada vez más grande y las ramas son más largas y parten más separadas desde la base sin interposición de un tramo basal. En las hembras, las ramas son más cortas, especialmente la anterior, y su trazado es rectilíneo en vez de curvo como en los machos. En los ejemplares seniles, las ramas son más cortas y de longitud más similar entre ellas. Es frecuente la presencia de ramas accesorias, así como irregularidades de este patrón básico. Los análisis discriminantes y de componentes principales realizados muestran una clara separación entre los morfotipos atribuidos a machos y a hembras. Existen importantes diferencias histológicas con las verdaderas astas que sugieren que el desmogue podría no haber sido anual. Se confirma que no se desarrolla hueso esponjoso y que la mineralización del protoasta progresa centrífugamente desde el centro hasta la periferia. El desmogue tiene lugar una vez que los tejidos están completamente mineralizados (muertos). A diferencia de otras protoastas, el ciclo en Dicrocerus era completo dado que están documentadas tanto la fase de muda del terciopelo, como la de exposición del hueso desnudo antes del desmogue. Dadas las similitudes en el ciclo de crecimiento, y dado que la base de la protoasta presenta parcialmente una estructura similar a la roseta, las protoastas de Dicrocerus y las astas parecen ser apéndices homólogos. Las diferencias histológicas podrían estar relacionadas con diferencias en el ciclo hormonal que regulaba su crecimiento. Diferencias que podrían guardar relación con el hecho que i) Dicrocerus vivió en ambientes tropicales, ii) las hembras también poseían protoastas. Cabe resaltar que las verdaderas astas aparecieron varios millones de años más tarde de que surgieran las protoastas y otros apéndices craneales en Ruminantia, y en coincidencia con la transición climática del Mioceno Medio.

En este trabajo se realiza la descripción de los fósiles de tortuga encontrados en los yacimientos del Aragoniense medio-superior de Monteagudo, Tarazona de Aragón, El Buste y La Ciesma. Además, se ha comparado la asociación paleoquelionológica descrita en estas localidades con la descrita en localidades más antiguas del mismo sector de la Cuenca del Ebro. La diferencia entre la asociación de la Biozona Z-A de las Bardenas Reales de Navarra y la descrita en el resto de las localidades puede deberse al medio sedimentario y/o a los cambios de humedad y temperatura relativas acaecidos a lo largo del Mioceno inferior-medio.

La combinación de las complejas estructuras y de los diversos materiales que integran los dientes, restringe nuestro conocimiento acerca de su biomecánica. En este sentido, el análisis de elementos finitos (AEF) es un método utilizado en ingeniería y en estudios biomecánicos para estimar el rendimiento y las variaciones producidas por las tensiones y las deformaciones en estructuras mecánicas o del esqueleto humano, así como en tejidos blandos. En contadas ocasiones se ha aplicado este método al problema de diseño biomecánico de animales y aún menos en grupos fósiles. En este trabajo presentamos los resultados preliminares obtenidos al generar un completo y complejo modelo en 3D de elementos finitos del molar superior de un ciervo extinto para estudiar su funcionalidad y propiedades mecánicas.

Se dan a conocer tres nuevos yacimientos de vertebrados en el borde meridional de la depresión del Ebro: Las Torcas (Oligoceno superior), Villanueva de Huerva (Aragoniense superior) y El Artigazo, al tiempo que se caracterizan tres unidades tectosedimentarias en el Terciario del sector del río Huerva comprendido entre el pantano de las Torcas y Villanueva. La situación de los yacimientos dentro de las unidades definidas, permite establecer precisiones sobre el significado cronoestratigráfico de las mismas, así como su correlación con las U.T.S. caracterizadas anteriormente en las cubetas Ibéricas de Montalbán y Alloza.

Hispanopithecus laietanus from the Late Miocene (9.8 Ma) of Can Llobateres 1 (CLL1; Vallès-Penedès Basin, NE Iberian Peninsula) represents one of the latest occurrences of fossil apes in Western mainland Europe, where they are last recorded at ∼9.5 Ma. The paleoenvironment of CLL1 is thus relevant for understanding the extinction of European hominoids. To refine paleoenvironmental inferences for CLL1, we apply ecometric models based on functional crown type (FCT) variables-a scoring scheme devised to capture macroscopic functional traits of occlusal shape and wear surfaces of herbivorous large mammal molars. Paleotemperature and paleoprecipitation estimates for CLL1 are provided based on published regional regression models linking average FCT of large herbivorous mammal communities to climatic conditions. A mapping to Whittaker's present-day biome classification is also attempted based on these estimates, as well as a case-based reasoning via canonical variate analysis of FCT variables from five relevant biomes. Estimates of mean annual temperature (25 °C) and mean annual precipitation (881 mm) classify CLL1 as a tropical seasonal forest/savanna, only in partial agreement with the canonical variate analysis results, which classify CLL1 as a tropical rainforest with a higher probability. The former biome agrees better with previous inferences derived from fossil plants and mammals, as well as preliminary isotopic data. The misclassification of CLL1 as a tropical forest is attributed to the mixture of forest-adapted taxa with others adapted to more open environments, given that faunal and plant composition indicates the presence of a dense wetland/riparian forest with more open woodlands nearby. The tested FCT ecometric approaches do not provide unambiguous biome classification for CLL1. Nevertheless, our results are consistent with those from other approaches, thus suggesting that FCT variables are potentially useful to investigate paleoenvironmental changes through time and space-including those that led to the extinction of European Miocene apes., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Venta Micena is an area containing several palaeontological sites marking the beginning of the Calabrian stage (Early Pleistocene). The richness of the fossil accumulation including species of Asian, African and European origin, makes Venta Micena a key site for the the palaeoecological and palaeoenvironmental study of southern Europe during the Early Pleistocene. Thus, research has been focused on Venta Micena 3, which was originally interpreted as a single palaeosurface associated with a marshy context, in which most of the fauna was accumulated by Pachycrocuta brevirostris. Recent excavations have unearthed a new site, Venta Micena 4, located in the same stratigraphic unit (Unit C) and in close proximity to Venta Micena 3. Here we show the first analyses regarding the taphonomic and spatial nature of this new site, defining two stratigraphic boundaries corresponding to two different depositional events. Furthermore, the taphonomic analyses of fossil remains seem to indicate a different accumulative agent than Pachycrocuta, thus adding more complexity to the palaeobiological interpretation of the Venta Micena area. These results contribute to the discussion of traditional interpretations made from Venta Micena 3.

Computational methods for estimating diversification rates from extant species phylogenetic trees have become abundant in evolutionary research. However, little evidence exists about how their outcome compares to a complementary and direct source of information: the fossil record. Furthermore, there is virtually no direct test for the congruence of evolutionary rates based on these two sources. This task is only achievable in clades with both a well-known fossil record and a complete phylogenetic tree. Here, we compare the evolutionary rates of ruminant mammals as estimated from their vast paleontological record--over 1200 species spanning 50 myr--and their living-species phylogeny. Significantly, our results revealed that the ruminant's fossil record and phylogeny reflect congruent evolutionary processes. The concordance is especially strong for the last 25 myr, when living groups became a dominant part of ruminant diversity. We found empirical support for previous hypotheses based on simulations and neontological data: The pattern captured by the tree depends on how clade specific the processes are and which clades are involved. Also, we report fossil evidence for a postradiation speciation slowdown coupled with constant, moderate extinction in the Miocene. The recent deceleration in phylogenetic rates is connected to rapid extinction triggered by recent climatic fluctuations., (© 2015 The Author(s). Evolution © 2015 The Society for the Study of Evolution.)

Key innovations are newly acquired structures that permit the performance of a new function and open new adaptive zones, and are, therefore, of paramount significance for understanding the history of the Ruminantia, particularly its diversification through the Miocene. Here we review and discuss what is known about these evolutionary novelties, with special emphasis on the appearance and evolution of cranial appendages and high-crowned (or hypsodont) teeth. Cranial appendages probably favored the diversification of pecorans by being structures strongly related to sexual selection, whereas the acquisition of hypsodont teeth could have expanded potential dietary breadth and allowed species to extend diets into the grazing range without eliminating browsing as a potential diet. When analyzed in conjunction with patterns of faunal diversity and in the context of climatic changes, it seems that the overall view that ruminant cranial appendages and hypsodonty may have started responding to increased patterns of seasonality and the opening-up of ecosystems is roughly valid. Instead, they occurred through several distinct pulses and varied widely among continents. This review is, to our knowledge, the first to highlight that the evolution of these innovations has been far from constant and uniform through time. Furthermore, we identify that both a first attempt to increase hypsodonty starting in the early Miocene and a first evolution of antlers and pronghorns were interrupted as a consequence of wide climatic fluctuations in the early-middle Miocene transition., (© 2013 International Society of Zoological Sciences, Institute of Zoology/Chinese Academy of Sciences and Wiley Publishing Asia Pty Ltd.)

Global climate shifts and ecological flexibility are two major factors that may affect rates of speciation and extinction across clades. Here, we connect past climate to changes in diet and diversification dynamics of ruminant mammals. Using novel versions of Multi-State Speciation and Extinction models, we explore the most likely scenarios for evolutionary transitions among diets in this clade and ask whether ruminant lineages with different feeding styles (browsing, grazing and mixed feeding) underwent differential rates of diversification concomitant with global temperature change. The best model of trait change had transitions from browsers to grazers via mixed feeding, with appreciable rates of transition to and from grazing and mixed feeding. Diversification rates in mixed-feeder and grazer lineages tracked the palaeotemperature curve, exhibiting higher rates during the Miocene thermal maxima. The origination of facultative mixed diet and grazing states may have triggered two adaptive radiations--one during the Oligocene-Miocene transition and the other during Middle-to-Late Miocene. Our estimate of mixed diets for basal lineages of both bovids and cervids is congruent with fossil evidence, while the reconstruction of browser ancestors for some impoverished clades--Giraffidae and Tragulidae--is not. Our results offer model-based neontological support to previous palaeontological findings and fossil-based hypothesis highlighting the importance of dietary innovations--especially mixed feeding--in the success of ruminants during the Neogene.

Carnivoran-dominated fossil sites provide precious insights into the diversity and ecology of species rarely recovered in the fossil record. The lower level assemblage of Batallones-1 fossil site (Late Miocene; Madrid Basin, Spain) has yielded one of the most abundant and diversified carnivoran assemblage ever known from the Cenozoic record of mammals. A comprehensive taphonomic study is carried out here in order to constrain the concentration mode of this remarkable assemblage. Another distinctive feature of Batallones-1 is that the accumulation of carnivoran remains took place in the context of a geomorphological landform (cavity formation through a piping process) practically unknown in the generation of fossil sites. Two characteristics of the assemblage highly restrict the probable causes for the accumulation of the remains: (1) the overwhelming number of carnivorans individuals; and (2) the mortality profiles estimated for the four most abundant taxa do not correspond to the classic mortality types but rather were the consequence of the behavior of the taxa. This evidence together with other taphonomic data supports the hypothesis that carnivoran individuals actively entered the cavity searching for resources (food or water) and were unable to exit. The scarcity of herbivores implies that the shaft was well visible and avoided by these taxa. Fossil bones exhibit a very good preservation state as a consequence of their deposition in the restricted and protective environment of the chamber. Batallones-1 had another assemblage (upper level assemblage) that was dominated by herbivore remains and that potentially corresponded to the final stages of the cavity filling.

In a recent paper, Eronen et al. (2010; hereafter EEFJ) observe differences in occlusal morphology, tooth crown height, and mesowear pattern between populations of the Miocene tridactyl equid Anchitherium from Spain and Germany, proposing that Spanish Anchitherium underwent adaptive evolution to local or regional arid conditions. However, these authors do not take into account the actual diversity of Iberian representatives of Anchitherium, or the fact that the Spanish fossils cover a wider temporal and geographical range than those from Germany. For these reasons, we suggest that their subsequent statistical work should be reconsidered., (© 2011 The Author(s). Evolution© 2011 The Society for the Study of Evolution.)

Background: Specialised leaf-eating is almost universally regarded as the ancestral state of all ruminants, yet little evidence can be cited in support of this assumption, apart from the fact that all early ruminants had low crowned cheek teeth. Instead, recent years have seen the emergence evidence contradicting the conventional view that low tooth crowns always indicate leaf-eating and high tooth crowns grass-eating., Results: Here we report the results of two independent palaeodietary reconstructions for one of the earliest deer, Procervulus ginsburgi from the Early Miocene of Spain, suggesting that despite having lower tooth crowns than any living ruminant, this species included a significant proportion of grass in its diet., Conclusion: The phylogenetic distribution of feeding styles strongly supports that leaf-grass mixed feeding was the original feeding style of deer, and that later dietary specialization on leaves or grass occurred independently in several lineages. Evidence for other ruminant clades suggests that facultative mixed feeding may in fact have been the primitive dietary state of the Ruminantia, which would have been morphologically expressed only under specific environmental factors.