2,570 research outputs found

    Influence of thermophysiology on thermal behavior: the essentials of categorization

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    Predicted energy use of dwellings often deviates from the actual energy use. Thermoregulatory behavior of the occupant might explain this difference. Such behavior is influenced by thermal sensation and thermal comfort. These subjective ratings in turn are linked to physiological parameters such as core and skin temperatures. However, it is unclear which physiological parameters best predict thermoregulatory behavior. The objective of this research was to study physiological parameters that potentially can be used to predict thermoregulatory behavior. Sixteen healthy females (18-30years) were exposed to two dynamic temperature protocols: a gradual increase (+4K/h, ranging from 24 degrees C to 32 degrees C) and a gradual decrease in ambient temperature (-4K/h, ranging from 24 degrees C to 16 degrees C). During the experiments physiological responses, thermal sensation, thermal preference and the intention of thermoregulatory behavior were measured. Thermal sensation is highly correlated with thermal preference (r=-0.933, P<0.001). The skin temperature of the wrist best predicts thermal sensation (R2=0.558, P<0.001) and therefore seems useful as a physiological parameter to predict the intention of thermoregulatory behavior. When the subjects are categorized based on their thermal sensation votes, more precise predictions of thermal sensation can be made. This categorization therefore can be of value for the determination of the actual energy use of occupant in dwellings

    Approximate Homomorphisms of Ternary Semigroups

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    A mapping f:(G1,[]1)→(G2,[]2)f:(G_1,[ ]_1)\to (G_2,[ ]_2) between ternary semigroups will be called a ternary homomorphism if f([xyz]1)=[f(x)f(y)f(z)]2f([xyz]_1)=[f(x)f(y)f(z)]_2. In this paper, we prove the generalized Hyers--Ulam--Rassias stability of mappings of commutative semigroups into Banach spaces. In addition, we establish the superstability of ternary homomorphisms into Banach algebras endowed with multiplicative norms.Comment: 10 page

    Electroweak Baryogenesis in Non-minimal Composite Higgs Models

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    We address electroweak baryogenesis in the context of composite Higgs models, pointing out that modifications to the Higgs and top quark sectors can play an important role in generating the baryon asymmetry. Our main observation is that composite Higgs models that include a light, gauge singlet scalar in the spectrum [as in the model based on the symmetry breaking pattern SO(6)/SO(5)], provide all necessary ingredients for viable baryogenesis. In particular, the singlet leads to a strongly first-order electroweak phase transition and introduces new sources of CP violation in dimension-five operators involving the top quark. We discuss the amount of baryon asymmetry produced and the experimental constraints on the model.Comment: 15 pages, 7 figure

    Early multidrug resistance, defined by changes in intracellular doxorubicin distribution, independent of P-glycoprotein.

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    Resistance to multiple antitumour drugs, mostly antibiotics or alkaloids, has been associated with a cellular plasma membrane P-glycoprotein (Pgp), causing energy-dependent transport of drugs out of cells. However, in many common chemotherapy resistant human cancers there is no overexpression of Pgp, which could explain drug resistance. In order to characterise early steps in multidrug resistance we have derived a series of P-glycoprotein-positive (Pgp/+) and P-glycoprotein-negative (Pgp/-) multidrug resistant cell lines, from a human non-small cell lung cancer cell line, SW-1573, by stepwise selection with increasing concentrations of doxorubicin. These cells were exposed to doxorubicin and its fluorescence in nucleus (N) and cytoplasm (C) was quantified with laserscan microscopy and image analysis. The fluorescence N/C ratio in parent cells was 3.8 and decreased both in Pgp/+ and Pgp/- cells with increasing selection pressure to 1.2-2.6 for cells with a resistance factor of 7-17. N/C ratios could be restored partly with verapamil only in Pgp/+ cells. N/C ratio measurements may define a general Pgp-independent type of defense of mammalian cells against certain anticancer agents which may precede Pgp expression in early doxorubicin resistance

    Probing for Invisible Higgs Decays with Global Fits

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    We demonstrate by performing a global fit on Higgs signal strength data that large invisible branching ratios Br_{inv} for a Standard Model (SM) Higgs particle are currently consistent with the experimental hints of a scalar resonance at the mass scale m_h ~ 124 GeV. For this mass scale, we find Br_{inv} < 0.64 (95 % CL) from a global fit to individual channel signal strengths supplied by ATLAS, CMS and the Tevatron collaborations. Novel tests that can be used to improve the prospects of experimentally discovering the existence of a Br_{inv} with future data are proposed. These tests are based on the combination of all visible channel Higgs signal strengths, and allow us to examine the required reduction in experimental and theoretical errors in this data that would allow a more significantly bounded invisible branching ratio to be experimentally supported. We examine in some detail how our conclusions and method are affected when a scalar resonance at this mass scale has couplings deviating from the SM ones.Comment: 32pp, 15 figures v2: JHEP version, ref added & comment added after Eq.

    Measurement of the quasi-elastic axial vector mass in neutrino-oxygen interactions

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    The weak nucleon axial-vector form factor for quasi-elastic interactions is determined using neutrino interaction data from the K2K Scintillating Fiber detector in the neutrino beam at KEK. More than 12,000 events are analyzed, of which half are charged-current quasi-elastic interactions nu-mu n to mu- p occurring primarily in oxygen nuclei. We use a relativistic Fermi gas model for oxygen and assume the form factor is approximately a dipole with one parameter, the axial vector mass M_A, and fit to the shape of the distribution of the square of the momentum transfer from the nucleon to the nucleus. Our best fit result for M_A = 1.20 \pm 0.12 GeV. Furthermore, this analysis includes updated vector form factors from recent electron scattering experiments and a discussion of the effects of the nucleon momentum on the shape of the fitted distributions.Comment: 14 pages, 10 figures, 6 table

    Measurement of the Branching Fraction for B- --> D0 K*-

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    We present a measurement of the branching fraction for the decay B- --> D0 K*- using a sample of approximately 86 million BBbar pairs collected by the BaBar detector from e+e- collisions near the Y(4S) resonance. The D0 is detected through its decays to K- pi+, K- pi+ pi0 and K- pi+ pi- pi+, and the K*- through its decay to K0S pi-. We measure the branching fraction to be B.F.(B- --> D0 K*-)= (6.3 +/- 0.7(stat.) +/- 0.5(syst.)) x 10^{-4}.Comment: 7 pages, 1 postscript figure, submitted to Phys. Rev. D (Rapid Communications

    Study of e+e- --> pi+ pi- pi0 process using initial state radiation with BABAR

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    The process e+e- --> pi+ pi- pi0 gamma has been studied at a center-of-mass energy near the Y(4S) resonance using a 89.3 fb-1 data sample collected with the BaBar detector at the PEP-II collider. From the measured 3pi mass spectrum we have obtained the products of branching fractions for the omega and phi mesons, B(omega --> e+e-)B(omega --> 3pi)=(6.70 +/- 0.06 +/- 0.27)10-5 and B(phi --> e+e-)B(phi --> 3pi)=(4.30 +/- 0.08 +/- 0.21)10-5, and evaluated the e+e- --> pi+ pi- pi0 cross section for the e+e- center-of-mass energy range 1.05 to 3.00 GeV. About 900 e+e- --> J/psi gamma --> pi+ pi- pi0 gamma events have been selected and the branching fraction B(J/psi --> pi+ pi- pi0)=(2.18 +/- 0.19)% has been measured.Comment: 21 pages, 37 postscript figues, submitted to Phys. Rev.

    Evidence for the Rare Decay B -> K*ll and Measurement of the B -> Kll Branching Fraction

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    We present evidence for the flavor-changing neutral current decay B→K∗ℓ+ℓ−B\to K^*\ell^+\ell^- and a measurement of the branching fraction for the related process B→Kℓ+ℓ−B\to K\ell^+\ell^-, where ℓ+ℓ−\ell^+\ell^- is either an e+e−e^+e^- or μ+μ−\mu^+\mu^- pair. These decays are highly suppressed in the Standard Model, and they are sensitive to contributions from new particles in the intermediate state. The data sample comprises 123×106123\times 10^6 Υ(4S)→BBˉ\Upsilon(4S)\to B\bar{B} decays collected with the Babar detector at the PEP-II e+e−e^+e^- storage ring. Averaging over K(∗)K^{(*)} isospin and lepton flavor, we obtain the branching fractions B(B→Kℓ+ℓ−)=(0.65−0.13+0.14±0.04)×10−6{\mathcal B}(B\to K\ell^+\ell^-)=(0.65^{+0.14}_{-0.13}\pm 0.04)\times 10^{-6} and B(B→K∗ℓ+ℓ−)=(0.88−0.29+0.33±0.10)×10−6{\mathcal B}(B\to K^*\ell^+\ell^-)=(0.88^{+0.33}_{-0.29}\pm 0.10)\times 10^{-6}, where the uncertainties are statistical and systematic, respectively. The significance of the B→Kℓ+ℓ−B\to K\ell^+\ell^- signal is over 8σ8\sigma, while for B→K∗ℓ+ℓ−B\to K^*\ell^+\ell^- it is 3.3σ3.3\sigma.Comment: 7 pages, 2 postscript figues, submitted to Phys. Rev. Let
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