15 research outputs found

    Caracterización de los sistemas palustres de Las Tablas de Daimiel durante el Cuaternario: textura y composición de sus barros micríticos

    Get PDF
    The National Park of Las Tablas de Daimiel contains a continuous record o f shallow-lacustrine and fluvial deposits, which was studied in a borehole, 38.5 m in depth. The borehole has three different parts that reflect important sedimentary changes. The lower part (17 m) consists of cal cite muds with some dolomite, gypsum moulds, gastropods, calcified root tissues and sponge spicules. It deposited in a shallow, mostly permanent lacustrine system of variable salinity. The middle part (8.6 m) is formed by calcitic muds with traces of dolomite and include diatoms, sponge spicules, ostracods and calcified filaments. It represents the sedimentation within a freshwater palustrine system. The upper part (12.9 m) is made of m¡critic muds with desiccation cracks, alveolar structures, gastropods, charophytes and intraclasts. It formed in a palustrine regime with clear desiccation events. Radiocarbon dating of samples situated between 8.1 and 12.6 m indicate an age of about 25,000 yr BP

    Sequential Loading of Cohesin Subunits during the First Meiotic Prophase of Grasshoppers

    Get PDF
    A previous version of this article appeared as an Early Online Release on January 2, 2007 (doi:10.1371/journal.pgen.0030028.eor).The cohesin complexes play a key role in chromosome segregation during both mitosis and meiosis. They establish sister chromatid cohesion between duplicating DNA molecules during S-phase, but they also have an important role during postreplicative double-strand break repair in mitosis, as well as during recombination between homologous chromosomes in meiosis. An additional function in meiosis is related to the sister kinetochore cohesion, so they can be pulled by microtubules to the same pole at anaphase I. Data about the dynamics of cohesin subunits during meiosis are scarce; therefore, it is of great interest to characterize how the formation of the cohesin complexes is achieved in order to understand the roles of the different subunits within them. We have investigated the spatio-temporal distribution of three different cohesin subunits in prophase I grasshopper spermatocytes. We found that structural maintenance of chromosome protein 3 (SMC3) appears as early as preleptotene, and its localization resembles the location of the unsynapsed axial elements, whereas radiation-sensitive mutant 21 (RAD21) (sister chromatid cohesion protein 1, SCC1) and stromal antigen protein 1 (SA1) (sister chromatid cohesion protein 3, SCC3) are not visualized until zygotene, since they are located in the synapsed regions of the bivalents. During pachytene, the distribution of the three cohesin subunits is very similar and all appear along the trajectories of the lateral elements of the autosomal synaptonemal complexes. However, whereas SMC3 also appears over the single and unsynapsed X chromosome, RAD21 and SA1 do not. We conclude that the loading of SMC3 and the non-SMC subunits, RAD21 and SA1, occurs in different steps throughout prophase I grasshopper meiosis. These results strongly suggest the participation of SMC3 in the initial cohesin axis formation as early as preleptotene, thus contributing to sister chromatid cohesion, with a later association of both RAD21 and SA1 subunits at zygotene to reinforce and stabilize the bivalent structure. Therefore, we speculate that more than one cohesin complex participates in the sister chromatid cohesion at prophase I.This work was supported by grants BFU2005–05668-C03–01, BFU2006–06655, BFU2005–01266, BFU2005–02431, and BFU2006–04406 from Ministerio de Educación y Ciencia, España, and grants 1001160016 and 11/BCB/013 from Universidad Autónoma de Madrid and Comunidad de Madrid. The Department of Immunology and Oncology was founded and is supported by the Spanish Council for Scientific Research (CSIC).Peer reviewe

    Registro paleoclimático del Pleistoceno Medio en el valle del rio Tajo.

    Get PDF
    The central region of the Iberian Peninsula has specific climatic characteristics that have affected the vegetation evolution along the Quaternary period. The scarce available paleoclimatic information has shown that the vegetation evolution did not follow the valid patterns for other regions, not only those for Europe regions but also those for other regions into the Iberian Peninsula. We present in this work three palynological records from alluvial deposits of the river Tajo that correspond, by datation and/or correlation with other well-dated deposits, to the Middle Pleistocene. The vegetation during this period was open mediterranean formations made up of mainly evergreen Quercus, Olea, Juniperus and Cistaceae, indicating the existence of a dry mediterranean climate. The vegetation evolution along the Middle Pleistocene, reconstructed from the three palynological records, also shows the development of more humid or more arid pulses into a general trend of increasing aridity during the Middle Pleistocene

    Sequential Loading of Cohesin Subunits during the First Meiotic Prophase of Grasshoppers

    Get PDF
    The cohesin complexes play a key role in chromosome segregation during both mitosis and meiosis. They establish sister chromatid cohesion between duplicating DNA molecules during S-phase, but they also have an important role during postreplicative double-strand break repair in mitosis, as well as during recombination between homologous chromosomes in meiosis. An additional function in meiosis is related to the sister kinetochore cohesion, so they can be pulled by microtubules to the same pole at anaphase I. Data about the dynamics of cohesin subunits during meiosis are scarce; therefore, it is of great interest to characterize how the formation of the cohesin complexes is achieved in order to understand the roles of the different subunits within them. We have investigated the spatio-temporal distribution of three different cohesin subunits in prophase I grasshopper spermatocytes. We found that structural maintenance of chromosome protein 3 (SMC3) appears as early as preleptotene, and its localization resembles the location of the unsynapsed axial elements, whereas radiation-sensitive mutant 21 (RAD21) (sister chromatid cohesion protein 1, SCC1) and stromal antigen protein 1 (SA1) (sister chromatid cohesion protein 3, SCC3) are not visualized until zygotene, since they are located in the synapsed regions of the bivalents. During pachytene, the distribution of the three cohesin subunits is very similar and all appear along the trajectories of the lateral elements of the autosomal synaptonemal complexes. However, whereas SMC3 also appears over the single and unsynapsed X chromosome, RAD21 and SA1 do not. We conclude that the loading of SMC3 and the non-SMC subunits, RAD21 and SA1, occurs in different steps throughout prophase I grasshopper meiosis. These results strongly suggest the participation of SMC3 in the initial cohesin axis formation as early as preleptotene, thus contributing to sister chromatid cohesion, with a later association of both RAD21 and SA1 subunits at zygotene to reinforce and stabilize the bivalent structure. Therefore, we speculate that more than one cohesin complex participates in the sister chromatid cohesion at prophase I

    Caracterización climática de las etapas áridas del Pleistoceno Superior en la Región Central Peninsular

    Get PDF
    Evidences from different paleoclimatic records have shown the existence of arid periods during the Upper Pleistocene and the Holocene in the central Iberian Peninsula. We present the palynological records from two aeolian deposits of central Iberian Peninsula which were developed during two of that arid periods in the Upper Pleistocene. One deposit is a clay dune, dated by OSL/TL on 22-23 ka, corresponding to the Last Glacial Maximum. The second deposit is a sand formation with massive structure and facies loess-like, dated by IRSL on I I ka, corresponding to the Younger Dryas event. Both palynological records confirm the existence of arid periods at 22-23 ka and at Ilka, showing a vegetation made up of Pinus, Juniperus and steppe-like taxa. The differences between both records indicate that the cold-and-arid climatic conditions were more intense and longer during the Last Glacial Maximum than during the Younger Dryas

    Quaternary fossil horses within the Prados-Guatén Depression (Pantoja de La Sagra, Toledo)

    Full text link
    Durante la primera reunión de campo del Grupo Madrileño de Cuaternario (GQM-AEQUA) se localizaron restos fragmentarios de dentición de caballos fósiles en los antiguos areneros de Pantoja de La Sagra (Toledo), actualmente en proceso de desmantelamiento y relleno. Ante la posibilidad de deterioro y pérdida los restos fueron recolectados y trasladados al Museo Nacional de Ciencias Naturales (CSIC, Madrid) donde se ha procedido a su análisis. Las piezas fósiles analizadas responden a un maxilar izquierdo con tres piezas dentales in situ (molares y premolares), y otras siete más aisladas. Todos los dientes aislados, junto con el fragmento de maxilar existente, corresponden a un adulto joven. Los restos fósiles se encontraban asociados a un nivel de arenas fluviales situado unos cuatro metros por debajo de la superficie de la Terraza de +15 m de la Depresión Prados-Guatén definida como un nivel perteneciente al tránsito Pleistoceno inferior-medio, del antiguo Sistema fluvial Manzanares-Guatén por Silva (1988). En concreto los niveles superiores de esta terraza han sido interpretados como resultado de la superposición de los últimos depósitos del antiguo sistema fluvial y los primeros asociados al relleno de la Depresión por tributarios de área fuente más local tras su abandono como consecuencia del proceso de captura del valle inferior del Manzanares por parte del Río Jarama al SW de la Ciudad de Madrid (Silva et al., 1988). Los caracteres morfológicos y morfométricos de las piezas dentarias permiten identificarlos como Equus ferus cf. mosbachensis cuya distribución bioestratigráfica abarca la parte final del Pleistoceno Medio (c.a. 500-200 ka B.P.). Junto a los restos fósiles aparecieron también escasos fragmentos líticos correspondientes a productos de lascado en sílex de difícil atribución tecnológica. Los restos fósiles analizados, indican que el depósito extensivo de arenas fluviales en el eje de la Depresión, culminó durante el final del Pleistoceno medio, y que la dinámica fluvial de la Depresión tras su proceso de abandono fue de hecho más activa de lo que se pensaba con la instalación de sistemas de arroyos relevantes alimentados por cabeceras locales antes del encajamiento definitivo actual de los arroyos Prados y Guatén.During the first field-meeting of the Madrid Quaternary Research Group (GQM-AEQUA) several fossil teeth remnants of horses were localised at the ancient sand-quarries of Pantoja de La Sagra (Toledo), which presently are abandoned and refilling in progress. The possibility of deterioration and loss of the localised fossils remnants induced by the quarry works, they were collected and taken away to the Museo Nacional de Ciencias Naturales (CSIC, Madrid) for their preservation and analysis. Fossil remains correspond to a left maxilla with two in situ molars, another one inset on its alveolar cavity, fragments of premolar cavities, as well as other seven more isolated teeth. These fossils were outcropping in a sandy level at four meters below the +15 m fluvial terrace surface of the axial sector of de Prados-Guatén Depression, which is considered the last fluvial level belonging to the ancient Manzanares-Guatén fluvial system during the Lower-Middle Pleistocene transit (Silva, 1988). In detail, the upper fluvial sediments of this particular terrace level were interpreted as the result of the overlapping between the last materials deposited by the ancient Manzanares-Guatén fluvial system and the first ones resulting from the readjustment of former tributaries after the abandonment of the Depression caused by fluvial capture of the Lower Manzanares Valley SW Madrid City. The morphological features of the oclusal surface of the horse teeth and morphometric comparative analyses indicate that they belong to the specie Equus ferus, and probably to the subspecie mosbachensis. However due to the bad definition of this group in Europe and the few individuals analysed the better classification is Equus ferus cf. mosbachensis. The bioestratigraphic distribution of this fossil horse group in Europe extends on the upper part of the Middle Pleistocene (c.a. 500-200 ka B.P.). Few lithic artefacts outcropped also associated to the fossil remains, constituted by laminar flakes of hard technological classification. Fossil remains analysed in this work joint to the unique previous quaternary fossil mammal described for the Prados-Guatén Depression constituted by Mammuthus meridionalis NESTI of the former quarry of Esquivias adjacent to the AVE railway line (Silva et al., 1988b; 1999). The chronostratigraphic attribution of the fossil horses (Upper Middle Pleistocene) described here indicate that fluvial sedimentary activity within the Depression was relevant after its abandonment. Ancient tributaries of the former Manzanares-Guatén fluvial system, feed by local-intrabasinal headwaters, reworked the previous sandy sediments triggering multiepisodic deposition during the upper part of the Middle Pleistocene, before the more recent eventual incision of present streams dissecting the Depression

    Restos de caballos fósiles cuaternarios en la depresión Prados-Guatén (Pantoja de la Sagra, Toledo)

    Get PDF
    Durante la primera reunión de campo del Grupo Madrileño de Cuaternario (GQM-AEQUA) se localizaron restos fragmentarios de dentición de caballos fósiles en los antiguos areneros de Pantoja de La Sagra (Toledo), actualmente en proceso de desmantelamiento y relleno. Ante la posibilidad de deterioro y pérdida los restos fueron recolectados y trasladados al Museo Nacional de Ciencias Naturales (CSIC, Madrid) donde se ha procedido a su análisis. Las piezas fósiles analizadas responden a un maxilar izquierdo con tres piezas dentales in situ (molares y premolares), y otras siete más aisladas. Todos los dientes aislados, junto con el fragmento de maxilar existente, corresponden a un adulto joven. Los restos fósiles se encontraban asociados a un nivel de arenas fluviales situado unos cuatro metros por debajo de la superficie de la Terraza de +15 m de la Depresión Prados-Guatén definida como un nivel perteneciente al tránsito Pleistoceno inferior-medio, del antiguo Sistema fluvial Manzanares-Guatén por Silva (1988). En concreto los niveles superiores de esta terraza han sido interpretados como resultado de la superposición de los últimos depósitos del antiguo sistema fluvial y los primeros asociados al relleno de la Depresión por tributarios de área fuente más local tras su abandono como consecuencia del proceso de captura del valle inferior del Manzanares por parte del Río Jarama al SW de la Ciudad de Madrid (Silva et al., 1988). Los caracteres morfológicos y morfométricos de las piezas dentarias permiten identificarlos como Equus ferus cf. mosbachensis cuya distribución bioestratigráfica abarca la parte final del Pleistoceno Medio (c.a. 500-200 ka B.P.). Junto a los restos fósiles aparecieron también escasos fragmentos líticos correspondientes a productos de lascado en sílex de difícil atribución tecnológica. Los restos fósiles analizados, indican que el depósito extensivo de arenas fluviales en el eje de la Depresión, culminó durante el final del Pleistoceno medio, y que la dinámica fluvial de la Depresión tras su proceso de abandono fue de hecho más activa de lo que se pensaba con la instalación de sistemas de arroyos relevantes alimentados por cabeceras locales antes del encajamiento definitivo actual de los arroyos Prados y Guatén.Peer reviewe

    Detección de la actividad antrópica durante el Holoceno reciente, a través de la asociación de palinomorfos polínicos y no polínicos en dos depósitos higroturbosos (El Berrueco y Rascafría) en la Sierra de Guadarrama, Madrid

    Get PDF
    La percepción palinológica de la actividad antrópica se basa en la utilización de los llamados indicadores polínicos de antropización (Iversen, 1949; Turner, 1964; Van Zeist, 1966; Berglund, 1969; Behre, 1981, 1986, 1988; Jalut, 1991; Richard, 1983, 1985, 1994a, 1994b, 1995, 1997); este es el caso de las asociaciones de los palinomorfos nitrófilos de carácter antropozoógeno y antrópico, asociados a los palinomorfos no polínicos de afinidad coprófila, que permiten la identificación del uso del territorio. En las secuencias polínicas de las turberas de la Tolla Collado de El Berrueco (El Berrueco, CAM) y de la Tolla de Los Grifos (Rascafría, CAM), los indicadores polínicos de antropización han puesto de manifiesto que el paisaje vegetal reconstruido, eminentemente herbáceo, está dominado por zonas de pastizal dedicadas a la ganadería, unas veces trashumante y otras, más sedentario. Por otro lado, la presencia de microfósiles no polínicos como Pseudoschizaea circula y Glomus cf. fasciculatum (Tipo 207), estarían relacionados posiblemente con el desarrollo de procesos erosivos in situ favorecidos por el sobrepastoreo. [ABSTRACT] [Pollen and no-pollen record to detecte human activity during Late Holocene environments in Guadarrama mountain range, Madrid (El Berrueco and Rascafría peats]. We present the results of a palynologycal analyses (pollen and non-Pollen Palynomorphs) carried out in two cores obtained of a deposit located in Guadarrama Range (Madrid. Spain). The principal aim is to obtain an association of pollen and non-Pollen Palynomorphs (Iversen, 1949; Turner, 1964; Van Zeist, 1966; Berglund, 1969; Behre, 1981, 1986, 1988; Jalut, 1991; Richard, 1983,1985, 1994a, 1994b, 1995, 1997) in order to define the human activity in the study area. Palynological data shows a landscape dominated by herbaceous plants, where we distinguish two groups with diferents affinities; one group is formed by the anthropogenic which determine human uses, the other group is dominate by anthropozoogenic taxa associated with animals. Coprophilous non-Pollen Palynomorphs that helped us to the interpretation are represented for the Types 55A, 113, 165 y 368. The fluctuations between both groups establish the different uses of the landscape. Pseudoschizaea circula and Glomus cf. fasciculatum (Tipo 207) presences, shows somme erosives phases due human activity

    SMC3 Location in Spermatogonial Cells and in First Meiotic Prophase in the Grasshopper <i>L. migratoria</i> Spermatocytes

    No full text
    <div><p>(A and B) SMC3 is uniformly scattered throughout the nuclei of the spermatogonial cells, with the exception of the periphery of the single X chromosome. Note that the X chromosome is located into a nuclear protrusion.</p> <p>(C and D) In this preleptotene spermatocyte, SMC3 appears forming thin cohesion axis threads. Note the absence of labeling in the X chromosome.</p> <p>(E and F) In leptotene, there is a continuous formation of thin and single SMC3 treads, uniformly distributed into the entire nucleus. Note that the width of the X chromosome SMC3 axis is similar to those present in the autosomes.</p> <p>(G and H) The onset of zygotene in grasshopper spermatocytes is characterized by the presence of one or two regions of synapsis initiation. These synapsed regions are clearly seen due to the doubleness of the SMC3 threads width.</p> <p>(I and J) Zygotene spermatocyte in which the “bouquet” configuration is evident.</p> <p>(K and L) Pachytene spermatocyte characterized by the complete synapsis of autosomes denoted by the double width of the SMC3 lines. A thinner axial signal is present in the unsynapsed X chromosome univalent.</p> <p>(M and N) Early diplotene, in which desynapsis is accompanied by a barbed wire–like aspect of the SMC3 lines.</p> <p>(O and P) Late diplotene spermatocyte in which SMC3 is located at the interchromatid domain. It is interesting to note that no signals are found at the centromere regions. (B, D, F, H, J, L, N, and P) correspond to the DAPI-stained chromatin of the spermatocytes. The position of the single sex chromosome is marked with an X. 3-D reconstructions of all the cells of this plate are available in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.0030028#pgen-0030028-sv001" target="_blank">Video S1</a>–<a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.0030028#pgen-0030028-sv008" target="_blank">S8</a>.</p></div
    corecore