6,659 research outputs found

    Motor regulation results in distal forces that bend partially disintegrated Chlamydomonas axonemes into circular arcs

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    The bending of cilia and flagella is driven by forces generated by dynein motor proteins. These forces slide adjacent microtubule doublets within the axoneme, the motile cytoskeletal structure. To create regular, oscilla- tory beating patterns, the activities of the axonemal dyneins must be coordinated both spatially and temporally. It is thought that coordination is mediated by stresses or strains, which build up within the moving axoneme, and somehow regulate dynein activity. While experimenting with axonemes subjected to mild proteolysis, we observed pairs of doublets associate with each other and form bends with almost constant curvature. By model- ing the statics of a pair of filaments, we show that the activity of the motors concentrates at the distal tips of the doublets. Furthermore, we show that this distribution of motor activity accords with models in which curvature, or curvature-induced normal forces, regulates the activity of the motors. These observations, together with our theoretical analysis, provide evidence that dynein activity can be regulated by curvature or normal forces, which may, therefore, play a role in coordinating the beating of cilia and flagella

    Detailed analysis of quantum phase transitions within the u(2)u(2) algebra

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    We analyze in detail the quantum phase transitions that arise in models based on the u(2)u(2) algebraic description for bosonic systems with two types of scalar bosons. First we discuss the quantum phase transition that occurs in hamiltonians that admix the two dynamical symmetry chains u(2)u(1)u(2)\supset u(1) and u(2)so(2)u(2)\supset so(2) by diagonalizing the problem exactly in the u(1)u(1) basis. Then we apply the coherent state formalism to determine the energy functional. Finally we show that a quantum phase transition of a different nature, but displaying similar characteristics, may arise also within a single chain just by including higher order terms in the hamiltonian.Comment: 5 figure

    Avaliação preliminar da reação de cultivares de trigo a brusone em condições de campo.

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    bitstream/item/119385/1/FOL-06040.pd

    Avaliação preliminar da reação de cultivares de trigo à brusone em condições de campo.

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    bitstream/item/84366/1/CNPT-COM.-TEC.-1-88.pd

    Totem: a case study in HEP

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    It is being proved that the neurochip \Totem{} is a viable solution for high quality and real time computational tasks in HEP, including event classification, triggering and signal processing. The architecture of the chip is based on a "derivative free" algorithm called Reactive Tabu Search (RTS), highly performing even for low precision weights. ISA, VME or PCI boards integrate the chip as a coprocessor in a host computer. This paper presents: 1) the state of the art and the next evolution of the design of \Totem{}; 2) its ability in the Higgs search at LHC as an example.Comment: Latex, elsart.sty, 5 pages, talk presented by I.Lazzizzera at CHEP97 (Berlin, April 1997

    Cross-cultural validation and measurement invariance of the Short Grit scale (Grit-S): preliminary results.

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    Preliminary results of a cross-cultural validation of the Grit -

    Analysis of a fluvial groynes system on hydraulic scale model

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    River morphodynamics and sediment transportSediment-structure interactio

    Geometric invariant theory approach to the determination of ground states of D-wave condensates in isotropic space

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    A complete and rigorous determination of the possible ground states for D-wave pairing Bose condensates is presented, using a geometrical invariant theory approach to the problem. The order parameter is argued to be a vector, transforming according to a ten dimensional real representation of the group G=G={\bf O}3_3\otimes{\bf U}1×_1\times . We determine the equalities and inequalities defining the orbit space of this linear group and its symmetry strata, which are in a one-to-one correspondence with the possible distinct phases of the system. We find 15 allowed phases (besides the unbroken one), with different symmetries, that we thoroughly determine. The group-subgroup relations between bordering phases are pointed out. The perturbative sixth degree corrections to the minimum of a fourth degree polynomial GG-invariant free energy, calculated by Mermin, are also determined.Comment: 27 revtex pages, 2 figures, use of texdraw; minor changes in the bibliography and in Table II
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