668 research outputs found

    Morphometric and Meristic Characterization of Native Chame Fish (Dormitator latifrons) in Ecuador Using Multivariate Analysis

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    Ecuador, a country exhibiting large developments in fish farming, has a great variety of freshwater native fish. Among these fish is the Dormitator latifrons or chame, which has characteristics that make its farming prone to occur at a quite-developed stage. However, morphological characterization is required to establish a conservation program. In this study, 300 chames were captured in the Manabi province (Ecuador) to analyze their morphostructural model and to evaluate the effects of sex and the production system through multivariant techniques. The fish from the farm presented morphological measurements that were statistically (p 0.05). The percentage of correct adscription was 84%, with larger errors in wild fish. The morphostructural model had a high homogeneity, with 89.95% significant correlations (p < 0.05), and wild male and female fish were more homogeneous. The farm fish were larger because of the higher food availability. Moreover, the species exhibited sexual dimorphism, although there were no great differences in the morphometric measurements. This study shows the great biodiversity that naturally exists in Ecuadorian rivers. Therefore, it is of great interest to develop a chame breeding and conservation program

    Functional brain networks reveal the existence of cognitive reserve and the interplay between network topology and dynamics

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    We investigated how the organization of functional brain networks was related to cognitive reserve (CR) during a memory task in healthy aging. We obtained the magnetoencephalographic functional networks of 20 elders with a high or low CR level to analyse the differences at network features. We reported a negative correlation between synchronization of the whole network and CR, and observed differences both at the node and at the network level in: the average shortest path and the network outreach. Individuals with high CR required functional networks with lower links to successfully carry out the memory task. These results may indicate that those individuals with low CR level exhibited a dual pattern of compensation and network impairment, since their functioning was more energetically costly to perform the task as the high CR group. Additionally, we evaluated how the dynamical properties of the different brain regions were correlated to the network parameters obtaining that entropy was positively correlated with the strength and clustering coefficient, while complexity behaved conversely. Consequently, highly connected nodes of the functional networks showed a more stochastic and less complex signal. We consider that network approach may be a relevant tool to better understand brain functioning in aging.Comment: Main manuscript: 23 pages including references, 20 pages text, 8 figures and supplementary information include

    Age differences in selected measures of physical fitness in young handball players

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    [EN] Objective: The aims of the present study were: 1) to calculate the change of direction (COD) deficit (using a modified version of the 505 test and 10 m sprint time), and (2) to examine the differences in linear sprint, jump and COD performances, as well as COD deficit, between under-13 (U13) and under-15 (U15) male handball players. Methods: One hundred and nineteen young male handball players (under-13 [U13; n = 82] and under-15 [U15; n = 37]). Tests included anthropometric measurements, countermovement jump (CMJ), triple leg-hop for distance, linear sprint test (5, 10 and 20 m), and a modified version of the 505 COD test. Results: Results showed moderate to very large differences (P 0.05). Conclusions: Our results suggest that during the transition from pre- to post-puberty, young handball players should focus on transferring their progressive improvements in strength, speed, and power capacities to COD performance.S

    Fitness Trade-Offs Determine the Role of the Molecular Chaperonin GroEL in Buffering Mutations

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    Molecular chaperones fold many proteins and their mutated versions in a cell and can sometimes buffer the phenotypic effect of mutations that affect protein folding. Unanswered questions about this buffering include the nature of its mechanism, its influence on the genetic variation of a population, the fitness trade-offs constraining this mechanism, and its role in expediting evolution. Answering these questions is fundamental to understand the contribution of buffering to increase genetic variation and ecological diversification. Here, we performed experimental evolution, genome resequencing, and computational analyses to determine the trade-offs and evolutionary trajectories of Escherichia coli expressing high levels of the essential chaperonin GroEL. GroEL is abundantly present in bacteria, particularly in bacteria with large loads of deleterious mutations, suggesting its role in mutational buffering. We show that groEL overexpression is costly to large populations evolving in the laboratory, leading to groE expression decline within 66 generations. In contrast, populations evolving under the strong genetic drift characteristic of endosymbiotic bacteria avoid extinction or can be rescued in the presence of abundant GroEL. Genomes resequenced from cells evolved under strong genetic drift exhibited significantly higher tolerance to deleterious mutations at high GroEL levels than at native levels, revealing that GroEL is buffering mutations in these cells. GroEL buffered mutations in a highly diverse set of proteins that interact with the environment, including substrate and ion membrane transporters, hinting at its role in ecological diversification. Our results reveal the fitness trade-offs of mutational buffering and how genetic variation is maintained in population

    A real-time scheduling framework on distributed mobile environments

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    Throughout the years, a centralized model has been widely used in all sorts of regarding computer science, educational and new technology applications, this distributed mobile system application structure partitions task or workloads between the provider and requester service. This work describes the implementation of a user graphical interface, named JPeer, for an embedded software; this shows the use of a P2P network that allows a supercomputer the allocation of its resources optimally among the different nodes connected to it. The peers in this project are represented as mobile devices and with the use of JNI (Java Native interface), with this it is possible to communicate peers created in Java with peers created in C++, accordingly, message passing would therefore be possible among different programming languages and operating systems. We applied several P2P nets with multiple peers in a node of LNS (supercomputing laboratory) in Southeast Mexico. The understanding of distributed and real time system algorithms can represent a difficulty due to the abstraction and difficult learning. In the meantime, the framework implementation represents a mobile distributed system environment, where the user can manage the nodes in a simple, easy and transparent way, as well as visualize how each node executes its processes, becomes a very useful and didactic tool. On the other hand, we highlight the need to adapt languages with native characteristics and take advantage of both parts on educational and technological environment

    Constitutive and Ghrelin-Dependent GHSR1a activation impairs CaV2.1 and CaV2.2 currents in hypothalamic neurons

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    The growth hormone secretagogue receptor type 1a (GHSR1a) has the highest known constitutive activity of any G Protein-Coupled receptor (GPCR). GHSR1a mediates the action of the hormone ghrelin, and its activation increases transcriptional and electrical activity in hypothalamic neurons. Although GHSR1a is present at GABAergic presynaptic terminals, its effect on neurotransmitter release remains unclear. The activities of the Voltage-Gated calcium channels, CaV2.1 and CaV2.2, which mediate neurotransmitter release at presynaptic terminals, are modulated by many GPCRs. Here, we show that both constitutive and Agonist-Dependent GHSR1a activity elicit a strong impairment of CaV2.1 and CaV2.2 currents in rat and mouse hypothalamic neurons and in a heterologous expression system. Constitutive GHSR1a activity reduces CaV2 currents by a Gi/o-Dependent mechanism that involves persistent reduction in channel density at the plasma membrane, whereas Ghrelin-Dependent GHSR1a inhibition is reversible and involves altered CaV2 gating via a Gq-Dependent pathway. Thus, GHSR1a differentially inhibits CaV2 channels by Gi/o or Gq protein pathways depending on its mode of activation. Moreover, we present evidence suggesting that GHSR1a-Mediated inhibition of CaV2 attenuates GABA release in hypothalamic neurons, a mechanism that could contribute to neuronal activation through the disinhibition of postsynaptic neurons.Instituto Multidisciplinario de Biología Celula

    Analysing biomarkers in oral fluid from pigs: influence of collection strategy and age of the pig

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    peer-reviewedBackground and objectives Oral fluid (OF) is an easy-to-collect, inexpensive, fast and non-invasive sample to characterize health and welfare status of the pig. However, further standardisation of the collection methods is needed in order to use it regularly in veterinary practice. Cotton ropes are routinely used to collect OF for pathogen detection but they may not be optimal for biomarker analysis due to sample contamination. This study compared two methods (cotton ropes and sponges) to collect porcine OF for biomarker analysis. A panel of 11 biomarkers of stress, inflammation, sepsis, immunity, redox status and general homeostasis was studied. Materials and methods Eighteen farrow-to-finish pig farms were included in the study. In each farm, three (for sponges) or four pens of pigs (for ropes) were sampled at four age categories: the week after weaning (5 weeks), before (11–12 weeks) and after (12–13 weeks) moving to finisher facility and the week before slaughter (22–25 weeks). In total, 288 OF samples were collected with cotton ropes and 216 with sponges and analysed for the biomarkers: cortisol, alpha-amylase, oxytocin (stress), haptoglobin (inflammation), procalcitonin (sepsis), adenosine deaminase, immunoglobulin G (immune system), ferric reducing antioxidant power (redox status), and creatine kinase, lactate dehydrogenase and total protein (general homeostasis). Samples were also scored visually for dirtiness using a score from 1 (clean) to 5 (very dirty). Results Rope-collected OF had higher levels of dirtiness (3.7 ± 0.04) compared to sponge-collected OF (2.7 ± 0.15) and had higher values than sponges for cortisol, procalcitonin, oxytocin, haptoglobin, total protein, lactate dehydrogenase and ferric reducing antioxidant power. All biomarkers decreased in value with age. Immunoglobulin G did not perform well for any of the two collection methods. Discussion and conclusion The results showed a clear effect of age on the biomarkers in OF collected with both, sponges or ropes. Sponges provided a cleaner sample than cotton ropes for biomarker analysis. Both methods are easy to apply under the commercial conditions in pig farms although sponges may take more time in early weaner stages. From a practical point of view, sampling with sponges achieved the best combination of reduced sampling time and low contamination

    Constitutive and Ghrelin-Dependent GHSR1a activation impairs CaV2.1 and CaV2.2 currents in hypothalamic neurons

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    The growth hormone secretagogue receptor type 1a (GHSR1a) has the highest known constitutive activity of any G Protein-Coupled receptor (GPCR). GHSR1a mediates the action of the hormone ghrelin, and its activation increases transcriptional and electrical activity in hypothalamic neurons. Although GHSR1a is present at GABAergic presynaptic terminals, its effect on neurotransmitter release remains unclear. The activities of the Voltage-Gated calcium channels, CaV2.1 and CaV2.2, which mediate neurotransmitter release at presynaptic terminals, are modulated by many GPCRs. Here, we show that both constitutive and Agonist-Dependent GHSR1a activity elicit a strong impairment of CaV2.1 and CaV2.2 currents in rat and mouse hypothalamic neurons and in a heterologous expression system. Constitutive GHSR1a activity reduces CaV2 currents by a Gi/o-Dependent mechanism that involves persistent reduction in channel density at the plasma membrane, whereas Ghrelin-Dependent GHSR1a inhibition is reversible and involves altered CaV2 gating via a Gq-Dependent pathway. Thus, GHSR1a differentially inhibits CaV2 channels by Gi/o or Gq protein pathways depending on its mode of activation. Moreover, we present evidence suggesting that GHSR1a-Mediated inhibition of CaV2 attenuates GABA release in hypothalamic neurons, a mechanism that could contribute to neuronal activation through the disinhibition of postsynaptic neurons.Instituto Multidisciplinario de Biología Celula

    Rate-control algorithms for non-embedded wavelet-based image coding

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    During the last decade, there has been an increasing interest in the design of very fast wavelet image encoders focused on specific applications like interactive real-time image and video systems, running on power-constrained devices such as digital cameras, mobile phones where coding delay and/or available computing resources (working memory and power processing) are critical for proper operation. In order to reduce complexity, most of these fast wavelet image encoders are non-(SNR)-embedded and as a consequence, precise rate control is not supported. In this work, we propose some simple rate control algorithms for these kind of encoders and we analyze their impact to determine if, despite their inclusion, the global encoder is still competitive with respect to popular embedded encoders like SPIHT and JPEG2000. In this study we focus on the non-embedded LTW encoder, showing that the increase in complexity due to the rate control algorithm inclusion, maintains LTW competitive with respect to SPIHT and JPEG2000 in terms of R/D performance, coding delay and memory consumption. © Springer Science+Business Media, LLC 2011This work was funded by Spanish Ministry of education and Science under grant DPI2007-66796-C03-03.Lopez Granado, OM.; Onofre Martinez-Rach, M.; Pinol Peral, P.; Oliver Gil, JS.; Perez Malumbres, MJ. (2012). Rate-control algorithms for non-embedded wavelet-based image coding. Journal of Signal Processing Systems. 68(2):203-216. https://doi.org/10.1007/s11265-011-0598-6S203216682Antonini, M., Barlaud, M., Mathieu, P., & Daubechies, I. (1992). Image coding using wavelet transform. IEEE Transaction on Image Processing, 1(2), 205–220.Cho, Y., & Pearlman, W.A. (2007). Hierarchical dynamic range coding of wavelet subbands for fast and efficient image compression. IEEE Transactions on Image Processing, 16, 2005–2015.Chrysafis, C., Said, A., Drukarev, A., Islam, A., & Pearlman, W. (2000). SBHP—A low complexity wavelet coder. In IEEE international conference on acoustics, speech and signal processing.CIPR: http://www.cipr.rpi.edu/resource/stills/kodak.html . Center for Image Processing Research.Davis, P. J. (1975) Interpolation and approximation. Dover Publications.Grottke, S., Richter, T., & Seiler, R. (2006). Apriori rate allocation in wavelet-based image compression. In Second international conference on automated production of cross media content for multi-channel distribution, 2006. AXMEDIS ’06 (pp. 329–336). doi: 10.1109/AXMEDIS.2006.12 .Guo, J., Mitra, S., Nutter, B., & Karp, T. (2006). Backward coding of wavelet trees with fine-grained bitrate control. Journal of Computers, 1(4), 1–7. doi: 10.4304/jcp.1.4.1-7 .ISO/IEC 10918-1/ITU-T Recommendation T.81 (1992). Digital compression and coding of continuous-tone still image.ISO/IEC 15444-1 (2000). JPEG2000 image coding system.Kakadu, S. (2006). http://www.kakadusoftware.com .Kasner, J., Marcellin, M., & Hunt, B. (1999). Universal trellis coded quantization. IEEE Transactions on Image Processing, 8(12), 1677–1687. doi: 10.1109/83.806615 .Lancaster, P. (1986). Curve and surface fitting: An introduction. Academic Press.Oliver, J., & Malumbres, M. (2001). A new fast lower-tree wavelet image encoder. In Proceedings of international conference on image processing, 2001 (Vol. 3, pp. 780–783). doi: 10.1109/ICIP.2001.958236 .Oliver, J., & Malumbres, M. P. (2006). Low-complexity multiresolution image compression using wavelet lower trees. IEEE Transactions on Circuits and Systems for Video Technology, 16(11), 1437–1444.Pearlman, W. A. (2001). Trends of tree-based, set partitioning compression techniques in still and moving image systems. In Picture coding symposium.Said, A., & Pearlman, A. (1996). A new, fast and efficient image codec based on set partitioning in hierarchical trees. IEEE Transactions on Circuits, Systems and Video Technology, 6(3), 243–250.Table Curve 3D 3.0 (1998). http://www.systat.com. Systat Software Inc.Wu, X. (2001). The transform and data compression handbook, chap. Compression of wavelet transform coefficients, (pp. 347–378). CRC Press.Zhidkov, N., & Kobelkov, G. (1987). Numerical methods. Moscow: Nauka
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