958 resultados para FOSSIL RECORD


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Using shells collected from a sediment trap series in the Madeira Basin, we investigate the effects of seasonal variation of temperature, productivity, and optimum growth conditions on calcification in three species of planktonic Foraminifera. The series covers an entire seasonal cycle and reflects conditions at the edge of the distribution of the studied species, manifesting more suitable growth conditions during different parts of the year. The seasonal variation in seawater carbonate saturation at the studied site is negligible compared to other oceanic regions, allowing us to assess the effect of parameters other than carbonate saturation. Shell calcification is quantified using weight and size of individual shells. The size-weight scaling within each species is robust against changes in environmental parameters, but differs among species. An analysis of the variation in calcification intensity (size-normalized weight) reveals species-specific response patterns. In Globigerinoides ruber (white) and Globigerinoides elongatus, calcification intensity is correlated with temperature (positive) and productivity (negative), whilst in Globigerina bulloides no environmental forcing is observed. The size-weight scaling, calcification intensity, and response of calcification intensity to environmental change differed between G. ruber (white) and G. elongatus, implying that patterns extracted from pooled analyses of these species may reflect their changing proportions in the samples. Using shell flux as a measure of optimum growth conditions, we observe significant positive correlation with calcification intensity in G. elongatus, but negative correlation in G. bulloides. The lack of a consistent response of calcification intensity to optimum growth conditions is mirrored by the results of shell size analyses. We conclude that calcification intensity in planktonic Foraminifera is affected by factors other than carbonate saturation. These factors include temperature, productivity, and optimum growth conditions, but the strength and sign of the relationships differ among species, potentially complicating interpretations of calcification data from the fossil record.

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The origins of some species of economic importance occurring over the Mediterranean Basin have been a traditional matter of debate that has important implications for land management. The case of Pinus pinea L. (Stone pine) is probably one of the most controversial, due to its documented long-term interaction with humans and its presence as a symbolic tree in certain areas of the Mediterranean (e.g., southwestern Iberia and Tuscany). Among the rest of the Mediterranean pines, several features make this pine unique (it has a characteristic crown shape, an edible kernel, cones that require three years to mature, and a very depauperate genetic diversity across its range). In addition, its palaeoecological information is rather limited, as the taxonomic precision attained by pollen analysts is insufficient for this tree and macroremains (such as kernels or anatomically well preserved wood) are needed to unequivocally detect the species in the fossil record. Recent findings of macrofossils of Pinus pinea in inland Iberia (Duero Basin) extend the late- Holocene range of the species, but the palaeobiogeographical information and the exhaustive genetic data available still suggest a very limited natural area (but still not sufficiently well defined) and a long and intense history of linkage to humans.

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En esta memoria de Tesis Doctoral se aborda el estudio paleobotánico de seis yacimientos tobáceos situados en las localidades burgalesas de Tubilla del Agua, Sedano, Herrán, Tobera y Frías, y en la alavesa de Ocio. El registro fósil encontrado en estos afloramientos se analiza de forma conjunta con el objetivo de conocer la evolución de la vegetación en el sector biogeográfico Castellano Cantábrico. Este sector se considera el territorio para el cual los hallazgos paleobotánicos son representativos y extrapolables, en tanto que constituye una región homogénea desde el punto de vista florístico, que abarca todos los yacimientos prospectados. El contexto temporal en el que se enmarca este estudio es el final del Cuaternario, desde el Pleistoceno Medio hasta la actualidad. Este intervalo se ha establecido a partir de la edad de los depósitos estudiados, la cual ha sido determinada —para los yacimientos de los que no se disponía de edades fiables— mediante la datación de muestras extraídas de las diferentes unidades litológicas identificadas. Para ello han sido empleadas las técnicas de carbono-14, desequilibrio de las series del uranio y racemización de aminoácidos. Los resultados geocronológicos obtenidos junto con el análisis geomorfológico de los yacimientos han permitido vincular la génesis de las 13 unidades litológicas identificadas con diferentes estadíos climáticos. Estos abarcan un amplio rango de condiciones ambientales, desde las más extremas del Último Máximo Glacial, hasta las más benignas de los Estadíos Isotópicos Marinos interglaciares 1 y 5. Como resultado de la prospección de los depósitos de toba fueron recuperados 1.820 fósiles, la mayoría impresiones foliares, pero también moldes de estróbilos femeninos, ramas y corteza, así como 42 carbones y restos subfósiles de Pinus sp. La identificación taxonómica de estos restos se ha realizado fundamentalmente a partir del análisis de caracteres diagnósticos morfológicos. Como resultado de ello, han sido descritos 28 taxones pertenecientes a las subclases Bryidae, Polypodiidae, Pinidae y Magnoliidae. La flora de los yacimientos estudiados se puede clasificar en tres grupos en función de sus requerimientos ecológicos: (i) uno formado por dos especies de alta tolerancia a la continentalidad —Pinus nigra y Quercus faginea—, las cuales aparecen bien representadas en la mayoría de los depósitos; (ii) otro constituido fundamentalmente por un conjunto de árboles y arbustos que habitualmente tienen el papel de especies acompañantes en los bosques ibéricos submediterráneos y eurosiberianos; y (iii) un tercer grupo compuesto por taxones hidrófitos o edafohigrófilos asociados al ecosistema del fitohermo activo y la vegetación de ribera. En el capítulo de Discusión se propone y analiza la hipótesis de que P. nigra y Q. faginea habrían sido las especies protagonistas de la vegetación zonal del sector Castellano Cantábrico durante el Cuaternario Final. Estas podrían haber persistido como tal incluso durante las épocas más frías, debido a su amplia valencia ecológica y a la capacidad de reproducirse vegetativamente en el caso del quejigo. Por el contrario, los taxones mesofíticos y eurosiberianos pudieron haber sufrido la expansión y retracción de sus poblaciones al ritmo de las oscilaciones climáticas. Sin embargo, la orografía diversa del sector Castellano Cantábrico proporciona emplazamientos en los que se combinan las diversas variables fisiográficas, de tal forma que pudieron haber existido microrrefugios en los que encontraron cobijo algunos taxones mesotérmicos y eurosiberianos durante los periodos glaciales. Por último, la historia evolutiva reciente de la vegetación de este territorio ha estado marcada por la acción antrópica, la cual empezó a ser manifiesta a partir del Neolítico. Esta se tradujo en la degradación y reducción de la cubierta forestal, así como en la extinción del pino laricio del Sector Castellano Cantábrico en los dos últimos milenios. ABSTRACT This PhD Dissertation focuses in the study of six tufa formations located nearby the villages of Tubilla del Agua, Sedano, Herrán, Tobera y Frías, all of them in the province of Burgos, and Ocio, which belongs to the province of Álava. We analyze the palaeobotanical archives of these sites with the purpose of unveiling and understanding the evolution of the vegetation of the Castilian Cantabrian biogeographical sector. This area is considered to be the territory that is represented in the palaeobotanical sample of the studied tufa archives. It is the homogeneous phitogeographical area with the lowest rank that include all the sites. The time frame of this study is the last part of the Quaternary, since the Middle Pleistocene to the present time. This interval is defined by the age of the tufa deposits, which were dated —for the ones that there were not available datings— throughout the analysis of 20 tufa samples taken from the 13 identified lithostratigraphic units. The age of the samples has been determined by using the methods of radiocarbon, U-Th dating and amino acid racemization. Chronological results, along with the chronostratigraphic study of the sites has allowed us to relate the build-up of the 13 identified lithostratigraphic units with different climatic stages. These structures were deposited in a wide range of climatic conditions, from the most extreme ones of the Last Glacial Maximum, to the warmer ones of the Marine Isotopic Stages 1 and 5. A total of 1,820 fossils were recovered from the tufa deposits, most of them were leaf impressions, but also pine cones, branches and bark moulds, along with charcoal and Pinus nigra macro remains. The taxonomical identification of these remains has been done mainly through the analysis of morphological traits. As a result of this process, 28 taxa belonging to the subclass of Bryidae, Polypodiidae, Pinidae and Magnoliidae were identified. The persistency of some taxa can be traced along different climatic stages in this fossil record. This fossil flora can be classified in three different groups: (i) the first one would be composed of two species with high continental climate tolerance —Pinus nigra y Quercus faginea—, which can be found in most of the deposits, (ii) the second group would be mostly formed by trees and shrubs that usually grow in the Iberian forests as an accessory species and (iii) the third one is composed of hydrophytes or hydrophilic taxa associate to the streams, riparian zones or the active tufa ecosystem. In the Discussion chapter we propose and analyse the hypothesis that P.nigra and Q. faginea were the main species of the zonal vegetation of the Castilian Cantabrian biogeographical sector during the last part of the Quaternary. This species could have persisted due to their wide ecological amplitude and also due to the capacity of asexual reproduction in the cases of the oak. On the other hand, mesophitic taxa could have suffered the retraction and expansion of their population following the climate oscillations. However, the diverse orography of the Castilian Cantabrian biogeographical sector provides a variety of combinations of physiographic variables, which could have been suitable refuges for some of the mesophitic taxa. The recent evolutionary history of the vegetation in this territory has been affected by human activities, which started to be relevant since the Neolithic. This led to a reduction of the forests and eventually, to the extinction of P. nigra in the Castilian Cantabrian biogeographical sector in the last two thousands of years.

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Analysis of several Salmonella typhimurium in vivo-induced genes located in regions of atypical base composition has uncovered acquired genetic elements that cumulatively engender pathogenicity. Many of these regions are associated with mobile elements, encode predicted adhesin and invasin-like functions, and are required for full virulence. Some of these regions distinguish broad host range from host-adapted Salmonella serovars and may contribute to inherent differences in host specificity, tissue tropism, and disease manifestation. Maintenance of this archipelago of acquired sequence by selection in specific hosts reveals a fossil record of the evolution of pathogenic species.

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Polycystine radiolaria are among few protistan groups that possess a comprehensive fossil record available for study by micropaleontologists. The Polycystinea and the Acantharea, whose skeletons do not become fossilized, were once members of the class “Radiolaria” (“Radiolaria” sensu lato: Polycystinea, Phaeodarea, and Acantharea) originally proposed by Haeckel but are now included in the superclass Actinopoda. Phylogenetic relationships within this superclass remain largely enigmatic. We investigated the evolutionary relationship of the Acantharea and the Polycystinea to other protists using phylogenetic analyses of 16S-like ribosomal RNA (rRNA) coding regions. We circumvented the need to culture these organisms by collecting and maintaining reproductive stages that contain many copies of their genomic DNA. This strategy facilitated extraction of genomic DNA and its purification from symbiont and prey DNA. Phylogenetic trees inferred from comparisons of 16S-like coding regions do not support a shared history between the Acantharea and the Polycystinea. However, the monophyly of the Acantharea and the separate monophyly of the Polycystinea (Spumellarida) are well supported by our molecular-based trees. The acantharian lineage branches among crown organisms whereas the polycystine lineage diverges before the radiation of the crown groups. We conclude that the Actinopoda does not represent a monophyletic evolutionary assemblage and recommend that this taxonomic designation be discarded.

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The past two decades have greatly improved our knowledge of vertebrate skeletal morphogenesis. It is now clear that bony morphology lacks individual descriptive specification and instead results from an interplay between positional information assigned during early limb bud deployment and its “execution” by highly conserved cellular response programs of derived connective tissue cells (e.g., chondroblasts and osteoblasts). Selection must therefore act on positional information and its apportionment, rather than on more individuated aspects of presumptive adult morphology. We suggest a trait classification system that can help integrate these findings in both functional and phylogenetic examinations of fossil mammals and provide examples from the human fossil record.

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For taxonomic levels higher than species, the abundance distributions of the number of subtaxa per taxon tend to approximate power laws but often show strong deviations from such laws. Previously, these deviations were attributed to finite-time effects in a continuous-time branching process at the generic level. Instead, we describe herein a simple discrete branching process that generates the observed distributions and find that the distribution's deviation from power law form is not caused by disequilibration, but rather that it is time independent and determined by the evolutionary properties of the taxa of interest. Our model predicts—with no free parameters—the rank-frequency distribution of the number of families in fossil marine animal orders obtained from the fossil record. We find that near power law distributions are statistically almost inevitable for taxa higher than species. The branching model also sheds light on species-abundance patterns, as well as on links between evolutionary processes, self-organized criticality, and fractals.

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Himalayacetus subathuensis is a new pakicetid archaeocete from the Subathu Formation of northern India. The type dentary has a small mandibular canal indicating a lack of auditory specializations seen in more advanced cetaceans, and it has Pakicetus-like molar teeth suggesting that it fed on fish. Himalayacetus is significant because it is the oldest archaeocete known and because it was found in marine strata associated with a marine fauna. Himalayacetus extends the fossil record of whales about 3.5 million years back in geological time, to the middle part of the early Eocene [≈53.5 million years ago (Ma)]. Oxygen in the tooth-enamel phosphate has an isotopic composition intermediate between values reported for freshwater and marine archaeocetes, indicating that Himalayacetus probably spent some time in both environments. When the temporal range of Archaeoceti is calibrated radiometrically, comparison of likelihoods constrains the time of origin of Archaeoceti and hence Cetacea to about 54–55 Ma (beginning of the Eocene), whereas their divergence from extant Artiodactyla may have been as early as 64–65 Ma (beginning of the Cenozoic).

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Mass extinctions have played many evolutionary roles, involving differential survivorship or selectivity of taxa and traits, the disruption or preservation of evolutionary trends and ecosystem organization, and the promotion of taxonomic and morphological diversifications—often along unexpected trajectories—after the destruction or marginalization of once-dominant clades. The fossil record suggests that survivorship during mass extinctions is not strictly random, but it often fails to coincide with factors promoting survival during times of low extinction intensity. Although of very serious concern, present-day extinctions have not yet achieved the intensities seen in the Big Five mass extinctions of the geologic past, which each removed ≥50% of the subset of relatively abundant marine invertebrate genera. The best comparisons for predictive purposes therefore will involve factors such as differential extinction intensities among regions, clades, and functional groups, rules governing postextinction biotic interchanges and evolutionary dynamics, and analyses of the factors that cause taxa and evolutionary trends to continue unabated, to suffer setbacks but resume along the same trajectory, to survive only to fall into a marginal role or disappear (“dead clade walking”), or to undergo a burst of diversification. These issues need to be addressed in a spatially explicit framework, because the fossil record suggests regional differences in postextinction diversification dynamics and biotic interchanges. Postextinction diversifications lag far behind the initial taxonomic and morphological impoverishment and homogenization; they do not simply reoccupy vacated adaptive peaks, but explore opportunities as opened and constrained by intrinsic biotic factors and the ecological and evolutionary context of the radiation.

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Coral reefs, with their millions of species, have changed profoundly because of the effects of people, and will continue to do so for the foreseeable future. Reefs are subject to many of the same processes that affect other human-dominated ecosystems, but some special features merit emphasis: (i) Many dominant reef builders spawn eggs and sperm into the water column, where fertilization occurs. They are thus particularly vulnerable to Allee effects, including potential extinction associated with chronic reproductive failure. (ii) The corals likely to be most resistant to the effects of habitat degradation are small, short-lived “weedy” corals that have limited dispersal capabilities at the larval stage. Habitat degradation, together with habitat fragmentation, will therefore lead to the establishment of genetically isolated clusters of inbreeding corals. (iii) Increases in average sea temperatures by as little as 1°C, a likely result of global climate change, can cause coral “bleaching” (the breakdown of coral–algal symbiosis), changes in symbiont communities, and coral death. (iv) The activities of people near reefs increase both fishing pressure and nutrient inputs. In general, these processes favor more rapidly growing competitors, often fleshy seaweeds, and may also result in explosions of predator populations. (v) Combinations of stress appear to be associated with threshold responses and ecological surprises, including devastating pathogen outbreaks. (vi) The fossil record suggests that corals as a group are more likely to suffer extinctions than some of the groups that associate with them, whose habitat requirements may be less stringent.

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The current massive degradation of habitat and extinction of species is taking place on a catastrophically short timescale, and their effects will fundamentally reset the future evolution of the planet's biota. The fossil record suggests that recovery of global ecosystems has required millions or even tens of millions of years. Thus, intervention by humans, the very agents of the current environmental crisis, is required for any possibility of short-term recovery or maintenance of the biota. Many current recovery efforts have deficiencies, including insufficient information on the diversity and distribution of species, ecological processes, and magnitude and interaction of threats to biodiversity (pollution, overharvesting, climate change, disruption of biogeochemical cycles, introduced or invasive species, habitat loss and fragmentation through land use, disruption of community structure in habitats, and others). A much greater and more urgently applied investment to address these deficiencies is obviously warranted. Conservation and restoration in human-dominated ecosystems must strengthen connections between human activities, such as agricultural or harvesting practices, and relevant research generated in the biological, earth, and atmospheric sciences. Certain threats to biodiversity require intensive international cooperation and input from the scientific community to mitigate their harmful effects, including climate change and alteration of global biogeochemical cycles. In a world already transformed by human activity, the connection between humans and the ecosystems they depend on must frame any strategy for the recovery of the biota.

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Global diversity curves reflect more than just the number of taxa that have existed through time: they also mirror variation in the nature of the fossil record and the way the record is reported. These sampling effects are best quantified by assembling and analyzing large numbers of locality-specific biotic inventories. Here, we introduce a new database of this kind for the Phanerozoic fossil record of marine invertebrates. We apply four substantially distinct analytical methods that estimate taxonomic diversity by quantifying and correcting for variation through time in the number and nature of inventories. Variation introduced by the use of two dramatically different counting protocols also is explored. We present sampling-standardized diversity estimates for two long intervals that sum to 300 Myr (Middle Ordovician-Carboniferous; Late Jurassic-Paleogene). Our new curves differ considerably from traditional, synoptic curves. For example, some of them imply unexpectedly low late Cretaceous and early Tertiary diversity levels. However, such factors as the current emphasis in the database on North America and Europe still obscure our view of the global history of marine biodiversity. These limitations will be addressed as the database and methods are refined.

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Clearly, the fossil record from the Cambrian period is an invaluable tool for deciphering animal evolution. Less clear, however, is how to integrate the paleontological information with molecular phylogeny and developmental biology data. Equally challenging is answering why the Cambrian period provided such a rich interval for the redeployment of genes that led to more complex bodyplans.

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SINE (short interspersed element) insertion analysis elucidates contentious aspects in the phylogeny of toothed whales and dolphins (Odontoceti), especially river dolphins. Here, we characterize 25 informative SINEs inserted into unique genomic loci during evolution of odontocetes to construct a cladogram, and determine a total of 2.8 kb per taxon of the flanking sequences of these SINE loci to estimate divergence times among lineages. We demonstrate that: (i) Odontocetes are monophyletic; (ii) Ganges River dolphins, beaked whales, and ocean dolphins diverged (in this order) after sperm whales; (iii) three other river dolphin taxa, namely the Amazon, La Plata, and Yangtze river dolphins, form a monophyletic group with Yangtze River dolphins being the most basal; and (iv) the rapid radiation of extant cetacean lineages occurred some 28–33 million years B.P., in strong accord with the fossil record. The combination of SINE and flanking sequence analysis suggests a topology and set of divergence times for odontocete relationships, offering alternative explanations for several long-standing problems in cetacean evolution.

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The fossil record of land plants is an obvious source of information on the dynamics of mass extinctions in the geological past. In conjunction with the end-Permian ecological crisis, ≈250 million years ago, palynological data from East Greenland reveal some unanticipated patterns. We document the significant time lag between terrestrial ecosystem collapse and selective extinction among characteristic Late Permian plants. Furthermore, ecological crisis resulted in an initial increase in plant diversity, instead of a decrease. Paradoxically, these floral patterns correspond to a “dead zone” in the end-Permian faunal record, characterized by a paucity of marine invertebrate megafossils. The time-delayed, end-Permian plant extinctions resemble modeled “extinction debt” responses of multispecies metapopulations to progressive habitat destruction.