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Discrete Character (discrete + character)
Selected AbstractsDiscrete modeling of the air-gap field of synchronous machines for computation of torque and radial forcesEUROPEAN TRANSACTIONS ON ELECTRICAL POWER, Issue 2 2008Marc Bekemans Abstract In this paper, we exploit the multiple symmetries and the discrete character of the current distribution to express the torque and the radial forces in a PM synchronous machine. Under some assumptions, the magnetic field can be built with a limited number of discrete functions. These functions can constitute an orthogonal base of a vector space for the representation of the machine magnetic state. The representation of the stator and rotor fields as vectors of this space makes it possible to interpret the torque and the radial forces from the concept of distance between these vectors. The proposed method for torque and radial forces computation is well suited for a real-time evaluation and can be used for a generalization of the Field-Oriented Control to machines with non-sinusoidal flux distribution. Copyright © 2007 John Wiley & Sons, Ltd. [source] Cohesive-zone models, higher-order continuum theories and reliability methods for computational failure analysis,INTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN ENGINEERING, Issue 1 2004René de Borst Abstract A concise overview is given of various numerical methods that can be used to analyse localization and failure in engineering materials. The importance of the cohesive-zone approach is emphasized and various ways to incorporate the cohesive-zone methodology in discretization methods are discussed. Numerical representations of cohesive-zone models suffer from a certain mesh bias. For discrete representations this is caused by the initial mesh design, while for smeared representations it is rooted in the ill-posedness of the rate boundary value problem that arises upon the introduction of decohesion. A proper representation of the discrete character of cohesive-zone formulations which avoids any mesh bias can be obtained elegantly when exploiting the partition-of-unity property of finite element shape functions. The effectiveness of the approach is demonstrated for some examples at different scales. Moreover, examples are shown how this concept can be used to obtain a proper transition from a plastifying or damaging continuum to a shear band with gross sliding or to a fully open crack (true discontinuum). When adhering to a continuum description of failure, higher-order continuum models must be used. Meshless methods are ideally suited to assess the importance of the higher-order gradient terms, as will be shown. Finally, regularized strain-softening models are used in finite element reliability analyses to quantify the probability of the emergence of various possible failure modes. Copyright © 2004 John Wiley & Sons, Ltd. [source] Autopodial skeleton evolution in side-necked turtles (Pleurodira)ACTA ZOOLOGICA, Issue 3 2007Marcelo R. Sánchez-Villagra Abstract Carpal and tarsal anatomy was documented based on the observation of dry skeletons of adult specimens representing 25 species in 15 genera and on data taken from the literature. In addition, histological sections and cleared and double-stained autopodia of recently hatched and juvenile specimens representing seven chelid and pelomedusoid species were studied. There is much more morphological diversity in the manus than in the pes. Variation in autopodial skeletons includes: the astragalus and calcaneum are either separated or fused; fusion of distal carpals 3,4,5 or just 4,5; number of centralia in the carpus; and presence/absence of a pisiform and of an accessory radial element. The widespread and probably basal phalangeal formula for Pleurodira is 2.3.3.3.3. Deviations are Pelomedusa subrufa, exhibiting a reduction to 2.2.2.2.2, Pelusios spp. with one phalanx less in digit I and for one species in digit V as well, and Acanthochelys pallidipectoris with an additional phalanx in the fourth finger. Six discrete characters itemizing some of the morphological variation observed were plotted on a composite pleurodire phylogeny, revealing not only homoplastic patterns but also the utility of some characters in supporting the monophyly of several clades. The pisiform is the last carpal element to ossify in Chelus fimbriatus. We hypothesize that the so-called fifth hooked metatarsal represents the fusion of distal tarsal 5 with metatarsal V. The accessory radial element that was occasionally present in the turtles examined may represent an atavism of the otherwise lost radiale of turtles. [source] Patterns of cryptic hybridization revealed using an integrative approach: a case study on genets (Carnivora, Viverridae, Genetta spp.) from the southern African subregionBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2005PHILIPPE GAUBERT Recent years have seen the development of molecular-based methodologies to investigate hybridization and its impact on the evolutionary process. However, morphological characterization of hybrid zones has only scantily been considered, especially in zootaxa. Thus, the level of congruence between molecular and morphological characters when attempting to detect hybrids remains a poorly tackled area. The genets (genus Genetta) provide an ideal case study for further investigation of the respective contribution of morphology and DNA in hybrid zone characterization because (1) their morphology has recently been exhaustively explored and (2) the existence of hybrid zones in southern Africa was proposed in the literature. We assessed levels of hybridization among the southern African genets, and questioned the role of ecological factors on the hybridization patterns detected. We used an integrative approach involving nine discrete morphological characters and a diagnostic discriminant function, geometric morphometrics and sequences of cytochrome b including collection specimens. The combination of independent materials allowed us to accurately reassess the level of hybridization in southern African genets, and revealed cryptic, interspecific gene flows. Morphology unambiguously detected a low number of G. maculata × G. tigrina hybrids and rejected the hypothesis of a large intergradation zone in KwaZulu-Natal, thus supporting the species status of the two genets. Cytochrome b analyses revealed: (1) cryptic, massive hybridization between G. tigrina and the sympatric G. felina, and (2) a trace of reticulation (one sequence) between G. tigrina and the allopatric G. genetta. The type specimen of G. mossambica Matschie, 1902 is considered to be a morphological hybrid between G. maculata and G. angolensis. Remarkably, the morphological approaches (discrete characters and morphometrics) proved complementary to conclusions derived from cytochrome b sequences. Whilst morphometrics was generally unable to accurately identify all putative hybrids, this approach revealed diagnostic cranial shape differences between recognized species as well as the cryptic G. ,letabae' (included in the super-species G. maculata). Morphometrics also confirmed the diagnostic value and age dependency of discrete characters. Our integrative approach appeared necessary to the detection of cryptic hybridizations and to the comprehensive characterization of hybrid zones. The recurrent detection of hybrids exhibiting tigrina -like coat patterns may suggest (1) asymmetric hybridization of G. tigrina males to females of other species and (2) positive selection for tigrina -like phenotype in South African habitats, but these hypotheses will have to be further tested using other sources of evidence. Despite the precise mosaic of hybrid zones identified in southern African genets, the environmental factors that shape patterns of distribution of hybrids remain unclear. Nevertheless, in the light of our range reassessment, it appears that seasonality of precipitation and periods of annual frost may play stringent roles in the distribution of genets. The complementarity of our results based on morphology and molecules is regarded as encouraging for the further development of integrative approaches in order to better understand the complex phenomena that underlie hybridization processes. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 86, 11,33. [source] | |||||||||||||