1,605 research outputs found

    Compilability of Abduction

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    Abduction is one of the most important forms of reasoning; it has been successfully applied to several practical problems such as diagnosis. In this paper we investigate whether the computational complexity of abduction can be reduced by an appropriate use of preprocessing. This is motivated by the fact that part of the data of the problem (namely, the set of all possible assumptions and the theory relating assumptions and manifestations) are often known before the rest of the problem. In this paper, we show some complexity results about abduction when compilation is allowed

    Analyzing Users' Activity in On-line Social Networks over Time through a Multi-Agent Framework

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    [EN] The number of people and organizations using online social networks as a new way of communication is continually increasing. Messages that users write in networks and their interactions with other users leave a digital trace that is recorded. In order to understand what is going on in these virtual environments, it is necessary systems that collect, process, and analyze the information generated. The majority of existing tools analyze information related to an online event once it has finished or in a specific point of time (i.e., without considering an in-depth analysis of the evolution of users activity during the event). They focus on an analysis based on statistics about the quantity of information generated in an event. In this article, we present a multi-agent system that automates the process of gathering data from users activity in social networks and performs an in-depth analysis of the evolution of social behavior at different levels of granularity in online events based on network theory metrics. We evaluated its functionality analyzing users activity in events on Twitter.This work is partially supported by the PROME-TEOII/2013/019, TIN2014-55206-R, TIN2015-65515-C4-1-R, H2020-ICT-2015-688095.Del Val Noguera, E.; Martínez, C.; Botti, V. (2016). Analyzing Users' Activity in On-line Social Networks over Time through a Multi-Agent Framework. Soft Computing. 20(11):4331-4345. https://doi.org/10.1007/s00500-016-2301-0S433143452011Ahn Y-Y, Han S, Kwak H, Moon S, Jeong H (2007) Analysis of topological characteristics of huge online social networking services. In: Proceedings of the 16th WWW, pp 835–844Bastiaensens S, Vandebosch H, Poels K, Cleemput KV, DeSmet A, Bourdeaudhuij ID (2014) Cyberbullying on social network sites. an experimental study into behavioural intentions to help the victim or reinforce the bully. Comput Hum Behav 31:259–271Benevenuto F, Rodrigues T, Cha M, Almeida V (2009) Characterizing user behavior in online social networks. In: Proceedings of the 9th ACM SIGCOMM conference on Internet measurement conference. ACM, pp 49–62Borge-Holthoefer J, Rivero A, García I, Cauhé E, Ferrer A, Ferrer D, Francos D, Iñiguez D, Pérez MP, Ruiz G et al (2011) Structural and dynamical patterns on online social networks: the Spanish may 15th movement as a case study. PLoS One 6(8):e23883Borondo J, Morales AJ, Losada JC, Benito RM (2013) Characterizing and modeling an electoral campaign in the context of Twitter: 2011 Spanish presidential election as a case studyCatanese SA, De Meo P, Ferrara E, Fiumara G, Provetti A (2011) Crawling facebook for social network analysis purposes. In: Proceedings of the international conference on web intelligence, mining and semantics. ACM, p 52Cha M, Mislove A, Gummadi KP (2009) A measurement-driven analysis of information propagation in the flickr social network. In: Proceedings of the 18th international conference on World Wide Web. ACM, pp 721–730del Val E, Martínez C, Botti V (2015a) A multi-agent framework for the analysis of users behavior over time in on-line social networks. In: 10th International conference on soft computing models in industrial and environmental applications. Springer, Berlin, pp 191–201del Val E, Rebollo M, Botti V (2015b) Does the type of event influence how user interactions evolve on twitter? PLOS One 10(5):e0124049Eurostat (2016a) Internet use statistics—individuals. http://ec.europa.eu/eurostat/statistics-explained/index.php/Internet_use_statistics_-_individuals . Accessed 29 April 2016Eurostat (2016b) Social media—statistics on the use by enterprises. http://ec.europa.eu/eurostat/statistics-explained/index.php/Social_media_-_statistics_on_the_use_by_enterprises#Further_Eurostat_information . Accessed 29 April 2016García Fornes AM, Rodrigo Solaz M, Terrasa Barrena AM, Inglada J, Javier V, Jorge Cano J, Mulet Mengual L, Palomares Chust A, Búrdalo Rapa LA, Giret Boggino AS et al (2015) Magentix 2 user’s manualGolbeck J, Robles C, Turner K (2011) Predicting personality with social media. In: CHI’11, pp 253–262Guimerà R, Llorente A, Moro E, Sales-Pardo M (2012) Predicting human preferences using the block structure of complex social networks. PloS One 7(9):e44620Huberman BA, Romero DM, Wu F (2008) Social networks that matter: Twitter under the microscope. arXiv preprint arXiv:0812.1045Jamali M, Abolhassani H (2006) Different aspects of social network analysis. In: 2006 IEEE/WIC/ACM international conference on web intelligence (WI 2006 main conference proceedings)(WI’06). IEEE, pp 66–72Jiang Y, Jiang J (2014) Understanding social networks from a multiagent perspective. Parallel Distrib Syst IEEE Trans 25(10):2743–2759Kossinets G, Watts D (2006) Empirical analysis of an evolving social network. Science 311(5757):88–90Kumar R, Novak J, Tomkins A (2010) Structure and evolution of online social networks. In: Yu PS, Han J, Faloutsos C (eds) Link mining: models, algorithms, and applications. Springer, New York, pp 337–357Lazer D (2009) Life in the network: the coming age of computational social science. Science 323(5915):721–723Leskovec J, Adamic LA, Huberman BA (2007) The dynamics of viral marketing. ACM Trans Web 1(1):5Licoppe C, Smoreda Z (2005) Are social networks technologically embedded? How networks are changing today with changes in communication technology. Soc Netw 27(4):317–335Lotan G, Graeff E, Ananny M, Gaffney D, Pearce I, Boyd D (2011) The revolutions were tweeted: information flows during the 2011 tunisian and egyptian revolutions. Int J Commun 5:1375–1405Peña-López I, Congosto M, Aragón P (2013) Spanish indignados and the evolution of 15M: towards networked para-institutions. Big data: challenges and opportunities, pp 25–26Perliger A, Pedahzur A (2011) Social network analysis in the study of terrorism and political violence. PS Polit Sci Polit 44:45–50Romero DM, Galuba W, Asur S, Huberman BA (2011a) Influence and passivity in social media. In: Proceedings of the 20th WWW, pp 113–114Romero DM, Meeder B, Kleinberg J (2011b) Differences in the mechanics of information diffusion across topics: idioms, political hashtags, and complex contagion on Twitter. In: Proceedings of the 20th WWW, pp 695–704Stockman FN, Doreian P, (1997) Evolution of social networks: processes and principles. In: Doreian P, Stokman FN (eds) Evolution of social networks. Routledge, London, pp 233–250Traud AL, Mucha PJ, Porter MA (2012) Social structure of facebook networks. Phys A Stat Mech Its Appl 391(16):4165–4180Ugander J, Karrer B, Backstrom L, Marlow C (2011) The anatomy of the Facebook social graph. arXiv preprint arXiv:1111.4503Valero S, del Val E, Alemany J, Botti V (2015) Using magentix2 in smart-home environments. In: 10th International conference on soft computing models in industrial and environmental applications. Springer, Berlin, pp 27–37Wasserman S, Faust K (1994) Social network analysis: methods and applications. Cambridge University Press, CambridgeWersm (2015) How much data is generated every minute on social media? http://wersm.com/how-much-data-is-generated-every-minute-on-social-media/ . Accessed 29 April 201

    Higgs boson decay into 2 photons in the type~II Seesaw Model

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    We study the two photon decay channel of the Standard Model-like component of the CP-even Higgs bosons present in the type II Seesaw Model. The corresponding cross-section is found to be significantly enhanced in parts of the parameter space, due to the (doubly-)charged Higgs bosons' (H±±)H±(H^{\pm \pm})H^\pm virtual contributions, while all the other Higgs decay channels remain Standard Model(SM)-like. In other parts of the parameter space H±±H^{\pm \pm} (and H±H^{\pm}) interfere destructively, reducing the two photon branching ratio tremendously below the SM prediction. Such properties allow to account for any excess such as the one reported by ATLAS/CMS at 125\approx 125 GeV if confirmed by future data; if not, for the fact that a SM-like Higgs exclusion in the diphoton channel around 114-115 GeV as reported by ATLAS, does not contradict a SM-like Higgs at LEP(!), and at any rate, for the fact that ATLAS/CMS exclusion limits put stringent lower bounds on the H±±H^{\pm \pm} mass, particularly in the parameter space regions where the direct limits from same-sign leptonic decays of H±±H^{\pm \pm} do not apply.Comment: 26 pages, 7 figure

    Caterpillars and fungal pathogens: two co-occurring parasites of an ant-plant mutualism

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    In mutualisms, each interacting species obtains resources from its partner that it would obtain less efficiently if alone, and so derives a net fitness benefit. In exchange for shelter (domatia) and food, mutualistic plant-ants protect their host myrmecophytes from herbivores, encroaching vines and fungal pathogens. Although selective filters enable myrmecophytes to host those ant species most favorable to their fitness, some insects can by-pass these filters, exploiting the rewards supplied whilst providing nothing in return. This is the case in French Guiana for Cecropia obtusa (Cecropiaceae) as Pseudocabima guianalis caterpillars (Lepidoptera, Pyralidae) can colonize saplings before the installation of their mutualistic Azteca ants. The caterpillars shelter in the domatia and feed on food bodies (FBs) whose production increases as a result. They delay colonization by ants by weaving a silk shield above the youngest trichilium, where the FBs are produced, blocking access to them. This probable temporal priority effect also allows female moths to lay new eggs on trees that already shelter caterpillars, and so to occupy the niche longer and exploit Cecropia resources before colonization by ants. However, once incipient ant colonies are able to develop, they prevent further colonization by the caterpillars. Although no higher herbivory rates were noted, these caterpillars are ineffective in protecting their host trees from a pathogenic fungus, Fusarium moniliforme (Deuteromycetes), that develops on the trichilium in the absence of mutualistic ants. Therefore, the Cecropia treelets can be parasitized by two often overlooked species: the caterpillars that shelter in the domatia and feed on FBs, delaying colonization by mutualistic ants, and the fungal pathogen that develops on old trichilia. The cost of greater FB production plus the presence of the pathogenic fungus likely affect tree growth

    Search for direct stau production in events with two hadronic tau-leptons in root s=13 TeV pp collisions with the ATLAS detector

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    A search for the direct production of the supersymmetric partners ofτ-leptons (staus) in final stateswith two hadronically decayingτ-leptons is presented. The analysis uses a dataset of pp collisions corresponding to an integrated luminosity of139fb−1, recorded with the ATLAS detector at the LargeHadron Collider at a center-of-mass energy of 13 TeV. No significant deviation from the expected StandardModel background is observed. Limits are derived in scenarios of direct production of stau pairs with eachstau decaying into the stable lightest neutralino and oneτ-lepton in simplified models where the two staumass eigenstates are degenerate. Stau masses from 120 GeV to 390 GeV are excluded at 95% confidencelevel for a massless lightest neutralino

    Magnitude and Timing of Leaf Damage Affect Seed Production in a Natural Population of Arabidopsis thaliana (Brassicaceae)

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    Background: The effect of herbivory on plant fitness varies widely. Understanding the causes of this variation is of considerable interest because of its implications for plant population dynamics and trait evolution. We experimentally defoliated the annual herb Arabidopsis thaliana in a natural population in Sweden to test the hypotheses that (a) plant fitness decreases with increasing damage, (b) tolerance to defoliation is lower before flowering than during flowering, and (c) defoliation before flowering reduces number of seeds more strongly than defoliation during flowering, but the opposite is true for effects on seed size. Methodology/Principal Findings: In a first experiment, between 0 and 75% of the leaf area was removed in May from plants that flowered or were about to start flowering. In a second experiment, 0, 25%, or 50% of the leaf area was removed from plants on one of two occasions, in mid April when plants were either in the vegetative rosette or bolting stage, or in mid May when plants were flowering. In the first experiment, seed production was negatively related to leaf area removed, and at the highest damage level, also mean seed size was reduced. In the second experiment, removal of 50% of the leaf area reduced seed production by 60% among plants defoliated early in the season at the vegetative rosettes, and by 22% among plants defoliated early in the season at the bolting stage, but did not reduce seed output of plants defoliated one month later. No seasonal shift in the effect of defoliation on seed size was detected. Conclusions/Significance: The results show that leaf damage may reduce the fitness of A. thaliana, and suggest that in this population leaf herbivores feeding on plants before flowering should exert stronger selection on defence traits than those feeding on plants during flowering, given similar damage levels

    Agronomic Management of Indigenous Mycorrhizas

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    Many of the advantages conferred to plants by arbuscular mycorrhiza (AM) are associated to the ability of AM plants to explore a greater volume of soil through the extraradical mycelium. Sieverding (1991) estimates that for each centimetre of colonized root there is an increase of 15 cm3 on the volume of soil explored, this value can increase to 200 cm3 depending on the circumstances. Due to the enhancement of the volume of soil explored and the ability of the extraradical mycelium to absorb and translocate nutrients to the plant, one of the most obvious and important advantages resulting from mycorrhization is the uptake of nutrients. Among of which the ones that have immobilized forms in soil, such as P, assume particular significance. Besides this, many other benefits are recognized for AM plants (Gupta et al, 2000): water stress alleviation (Augé, 2004; Cho et al, 2006), protection from root pathogens (Graham, 2001), tolerance to toxic heavy metals and phytoremediation (Audet and Charest, 2006; Göhre and Paszkowski, 2006), tolerance to adverse conditions such as very high or low temperature, high salinity (Sannazzaro et al, 2006), high or low pH (Yano and Takaki, 2005) or better performance during transplantation shock (Subhan et al, 1998). The extraradical hyphae also stabilize soil aggregates by both enmeshing soil particles (Miller e Jastrow, 1992) and producing a glycoprotein, golmalin, which may act as a glue-like substance to adhere soil particles together (Wright and Upadhyaya, 1998). Despite the ubiquous distribution of mycorrhizal fungi (Smith and Read, 2000) and only a relative specificity between host plants and fungal isolates (McGonigle and Fitter, 1990), the obligate nature of the symbiosis implies the establishment of a plant propagation system, either under greenhouse conditions or in vitro laboratory propagation. These techniques result in high inoculum production costs, which still remains a serious problem since they are not competitive with production costs of phosphorus fertilizer. Even if farmers understand the significance of sustainable agricultural systems, the reduction of phosphorus inputs by using AM fungal inocula alone cannot be justified except, perhaps, in the case of high value crops (Saioto and Marumoto, 2002). Nurseries, high income horticulture farmers and no-agricultural application such as rehabilitation of degraded or devegetated landscapes are examples of areas where the use of commercial inoculum is current. Another serious problem is quality of commercial available products concerning guarantee of phatogene free content, storage conditions, most effective application methods and what types to use. Besides the information provided by suppliers about its inoculum can be deceiving, as from the usually referred total counts, only a fraction may be effective for a particular plant or in specific soil conditions. Gianinazzi and Vosátka (2004) assume that progress should be made towards registration procedures that stimulate the development of the mycorrhizal industry. Some on-farm inoculum production and application methods have been studied, allowing farmers to produce locally adapted isolates and generate a taxonomically diverse inoculum (Mohandas et al, 2004; Douds et al, 2005). However the inocula produced this way are not readily processed for mechanical application to the fields, being an obstacle to the utilization in large scale agriculture, especially row crops, moreover it would represent an additional mechanical operation with the corresponding economic and soil compaction costs. It is well recognized that inoculation of AM fungi has a potential significance in not only sustainable crop production, but also environmental conservation. However, the status quo of inoculation is far from practical technology that can be widely used in the field. Together a further basic understanding of the biology and diversity of AM fungi is needed (Abbott at al, 1995; Saito and Marumoto, 2002). Advances in ecology during the past decade have led to a much more detailed understanding of the potential negative consequences of species introductions and the potential for negative ecological consequences of invasions by mycorrhizal fungi is poorly understood. Schwartz et al, (2006) recommend that a careful assessment documenting the need for inoculation, and the likelihood of success, should be conducted prior to inoculation because inoculations are not universally beneficial. Agricultural practices such as crop rotation, tillage, weed control and fertilizer apllication all produce changes in the chemical, physical and biological soil variables and affect the ecological niches available for occupancy by the soil biota, influencing in different ways the symbiosis performance and consequently the inoculum development, shaping changes and upset balance of native populations. The molecular biology tools developed in the latest years have been very important for our perception of these changes, ensuing awareness of management choice implications in AM development. In this context, for extensive farming systems and regarding environmental and economic costs, the identification of agronomic management practices that allow controlled manipulation of the fungal community and capitalization of AM mutualistic effect making use of local inoculum, seem to be a wise option for mycorrhiza promotion and development of sustainable crop production

    Análisis de programas de mejora continua. Un estudio longitudinal en una empresa industrial

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    Las empresas han utilizado diversas herramientas que permiten que los operarios contribuyan al proceso de mejora continua. Entre las herramientas más usadas podemos destacar los sistemas de sugerencias tanto individuales como en grupo. En esta comunicación haremos un repaso de las principales características de ambos sistemas y los modos habituales de implantación. Nuestra ponencia pretende intentar responder a estas preguntas de investigación. ¿Qué resultados se derivan de la implantación de sistemas de sugerencias individuales o en grupo? ¿Cuál de los dos sistemas es más beneficioso para la empresa? ¿Qué problemas surgen durante el funcionamiento de estos programas? Para ello, analizaremos los datos de un caso de empresa industrial donde hemos recogido los datos históricos de 5 años de aplicación de un programa de mejora continua. Ambos programas han demostrado ser provechosos para la empresa, aunque las posibilidades de los sistemas de grupo parecen ser significativamente mayores

    A framework to move forward on the path to eco-innovation in the construction industry: implications to improve firms´ sustainable orientation

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    This paper examines key aspects in the innovative behavior of the construction firms that determine their environmental orientation while innovating. Structural equation modeling was used and data of 222 firms retrieved from the Spanish Technological Innovation Panel (PITEC) for 2010 to analyse the drivers of environmental orientation of the construction firms during the innovation process. The results show that the environmental orientation is positively affected by the product and process orientation of construction firms during the innovation process. Furthermore, the positive relation between the importance of market information sources and environmental orientation, mediated by process and product orientation, is discussed. Finally, a model that explains these relations is proposed and validated. 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    Dinucleotide controlled null models for comparative RNA gene prediction

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    <p>Abstract</p> <p>Background</p> <p>Comparative prediction of RNA structures can be used to identify functional noncoding RNAs in genomic screens. It was shown recently by Babak <it>et al</it>. [BMC Bioinformatics. 8:33] that RNA gene prediction programs can be biased by the genomic dinucleotide content, in particular those programs using a thermodynamic folding model including stacking energies. As a consequence, there is need for dinucleotide-preserving control strategies to assess the significance of such predictions. While there have been randomization algorithms for single sequences for many years, the problem has remained challenging for multiple alignments and there is currently no algorithm available.</p> <p>Results</p> <p>We present a program called SISSIz that simulates multiple alignments of a given average dinucleotide content. Meeting additional requirements of an accurate null model, the randomized alignments are on average of the same sequence diversity and preserve local conservation and gap patterns. We make use of a phylogenetic substitution model that includes overlapping dependencies and site-specific rates. Using fast heuristics and a distance based approach, a tree is estimated under this model which is used to guide the simulations. The new algorithm is tested on vertebrate genomic alignments and the effect on RNA structure predictions is studied. In addition, we directly combined the new null model with the RNAalifold consensus folding algorithm giving a new variant of a thermodynamic structure based RNA gene finding program that is not biased by the dinucleotide content.</p> <p>Conclusion</p> <p>SISSIz implements an efficient algorithm to randomize multiple alignments preserving dinucleotide content. It can be used to get more accurate estimates of false positive rates of existing programs, to produce negative controls for the training of machine learning based programs, or as standalone RNA gene finding program. Other applications in comparative genomics that require randomization of multiple alignments can be considered.</p> <p>Availability</p> <p>SISSIz is available as open source C code that can be compiled for every major platform and downloaded here: <url>http://sourceforge.net/projects/sissiz</url>.</p
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