229 research outputs found

    A Lotka–Volterra type food chain model with stage structure and time delays

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    AbstractA three-species Lotka–Volterra type food chain model with stage structure and time delays is investigated. It is assumed in the model that the individuals in each species may belong to one of two classes: the immatures and the matures, the age to maturity is presented by a time delay, and that the immature predators (immature top predators) do not have the ability to feed on prey (predator). By using some comparison arguments, we first discuss the permanence of the model. By means of an iterative technique, a set of easily verifiable sufficient conditions are established for the global attractivity of the nonnegative equilibria of the model

    Sturm-Liouville operators on time scales

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    We establish the connection between Sturm-Liouville equations on time scales and Sturm--Liouville equations with measure-valued coefficients. Based on this connection we generalize several results for Sturm-Liouville equations on time scales which have been obtained by various authors in the past.Comment: 12 page

    Radiative Corrections to Fixed Target Moller Scattering Including Hard Bremsstrahlung Effects

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    We present a calculation of the complete O(α)O(\alpha) electroweak radiative corrections to the Moller scattering process e^-e^- -> e^-e^-, including hard bremsstrahlung contributions. We study the effects of these corrections on both the total cross section and polarization asymmetry measured in low energy fixed target experiments. Numerical results are presented for the experimental cuts relevant for E-158, a fixed target e^-e^- experiment being performed at SLAC; the effect of hard bremsstrahlung is to shift the measured polarization asymmetry by approximately +4%. We briefly discuss the remaining theoretical uncertainty in the prediction for the low energy Moller scattering polarization asymmetry.Comment: 22 pgs; minor clarifications added and typos fixe

    Quantifying the interdisciplinarity of scientific journals and fields

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    There is an overall perception of increased interdisciplinarity in science, but this is difficult to confirm quantitatively owing to the lack of adequate methods to evaluate subjective phenomena. This is no different from the difficulties in establishing quantitative relationships in human and social sciences. In this paper we quantified the interdisciplinarity of scientific journals and science fields by using an entropy measurement based on the diversity of the subject categories of journals citing a specific journal. The methodology consisted in building citation networks using the Journal Citation Reports database, in which the nodes were journals and edges were established based on citations among journals. The overall network for the 11-year period (1999-2009) studied was small-world and scale free with regard to the in-strength. Upon visualizing the network topology an overall structure of the various science fields could be inferred, especially their interconnections. We confirmed quantitatively that science fields are becoming increasingly interdisciplinary, with the degree of interdisplinarity (i.e. entropy) correlating strongly with the in-strength of journals and with the impact factor.Comment: 23 pages, 6 figure

    Invisible Z-Boson Decays at e+e- Colliders

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    The measurement of the invisible Z-boson decay width at e+e- colliders can be done "indirectly", by subtracting the Z-boson visible partial widths from the Z-boson total width, or "directly", from the process e+e- -> \gamma \nu \bar{\nu}. Both procedures are sensitive to different types of new physics and provide information about the couplings of the neutrinos to the Z-boson. At present, measurements at LEP and CHARM II are capable of constraining the left-handed Z\nu\nu-coupling, 0.45 <~ g_L <~ 0.5, while the right-handed one is only mildly bounded, |g_R| <= 0.2. We show that measurements at a future e+e- linear collider at different center-of-mass energies, \sqrt{s} = MZ and \sqrt{s}s ~ 170 GeV, would translate into a markedly more precise measurement of the Z\nu\nu-couplings. A statistically significant deviation from Standard Model predictions will point toward different new physics mechanisms, depending on whether the discrepancy appears in the direct or the indirect measurement of the invisible Z-width. We discuss some scenarios which illustrate the ability of different invisible Z-boson decay measurements to constrain new physics beyond the Standard Model

    Effective Lagrangian Approach to the Theory of Eta Photoproduction in the N(1535)N^{*}(1535) Region

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    We investigate eta photoproduction in the N(1535)N^{*}(1535) resonance region within the effective Lagrangian approach (ELA), wherein leading contributions to the amplitude at the tree level are taken into account. These include the nucleon Born terms and the leading tt-channel vector meson exchanges as the non-resonant pieces. In addition, we consider five resonance contributions in the ss- and uu- channel; besides the dominant N(1535)N^{*}(1535), these are: N(1440),N(1520),N(1650)N^{*}(1440),N^{*}(1520),N^{*}(1650) and N(1710)N^{*}(1710). The amplitudes for the π\pi^\circ and the η\eta photoproduction near threshold have significant differences, even as they share common contributions, such as those of the nucleon Born terms. Among these differences, the contribution to the η\eta photoproduction of the ss-channel excitation of the N(1535)N^{*}(1535) is the most significant. We find the off-shell properties of the spin-3/2 resonances to be important in determining the background contributions. Fitting our effective amplitude to the available data base allows us to extract the quantity χΓηA1/2/ΓT\sqrt{\chi \Gamma_\eta} A_{1/2}/\Gamma_T, characteristic of the photoexcitation of the N(1535)N^{*}(1535) resonance and its decay into the η\eta-nucleon channel, of interest to precise tests of hadron models. At the photon point, we determine it to be (2.2±0.2)×101GeV1(2.2\pm 0.2)\times 10^{-1} GeV^{-1} from the old data base, and (2.2±0.1)×101GeV1(2.2\pm 0.1) \times 10^{-1} GeV^{-1} from a combination of old data base and new Bates data. We obtain the helicity amplitude for N(1535)γpN^{*}(1535)\rightarrow \gamma p to be A1/2=(97±7)×103GeV1/2A_{1/2}=(97\pm 7)\times 10^{-3} GeV^{-1/2} from the old data base, and A1/2=(97±6)×103GeV1/2A_{1/2}=(97\pm 6)\times 10^{-3} GeV^{-1/2} from the combination of the old data base and new Bates data, compared with the results of the analysis of pion photoproduction yielding 74±1174\pm 11, in the same units.Comment: 43 pages, RevTeX, 9 figures available upon request, to appear in Phys. Rev.

    A Model for the Development of the Rhizobial and Arbuscular Mycorrhizal Symbioses in Legumes and Its Use to Understand the Roles of Ethylene in the Establishment of these two Symbioses

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    We propose a model depicting the development of nodulation and arbuscular mycorrhizae. Both processes are dissected into many steps, using Pisum sativum L. nodulation mutants as a guideline. For nodulation, we distinguish two main developmental programs, one epidermal and one cortical. Whereas Nod factors alone affect the cortical program, bacteria are required to trigger the epidermal events. We propose that the two programs of the rhizobial symbiosis evolved separately and that, over time, they came to function together. The distinction between these two programs does not exist for arbuscular mycorrhizae development despite events occurring in both root tissues. Mutations that affect both symbioses are restricted to the epidermal program. We propose here sites of action and potential roles for ethylene during the formation of the two symbioses with a specific hypothesis for nodule organogenesis. Assuming the epidermis does not make ethylene, the microsymbionts probably first encounter a regulatory level of ethylene at the epidermis–outermost cortical cell layer interface. Depending on the hormone concentrations there, infection will either progress or be blocked. In the former case, ethylene affects the cortex cytoskeleton, allowing reorganization that facilitates infection; in the latter case, ethylene acts on several enzymes that interfere with infection thread growth, causing it to abort. Throughout this review, the difficulty of generalizing the roles of ethylene is emphasized and numerous examples are given to demonstrate the diversity that exists in plants
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