730 research outputs found

    Higher order QCD corrections to the transverse and longitudinal fragmentation functions in electron-positron annihilation

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    We present the calculation of the order αs2\alpha_s^2 corrections to the coefficient functions contributing to the longitudinal (FL(x,Q2)F_L(x,Q^2)) and transverse fragmentation functions (FT(x,Q2)F_T(x,Q^2)) measured in electron-positron annihilation. The effect of these higher order QCD corrections on the behaviour of the fragmentation functions and the corresponding longitudinal (dσL(x,Q2)/dxd\sigma_L(x,Q^2)/dx) and transverse cross sections (dσT(x,Q2)/dxd\sigma_T(x,Q^2)/dx) are studied. In particular we investigate the dependence of the above quantities on the mass factorization scale (MM) and the various parameterizations chosen for the parton fragmentation densities DpH(x,M2)D_p^H(x,M^2) (p=q,gp=q,g; H=π±,K±,P,PˉH=\pi^\pm, K^\pm, P, \bar{P}). Our analysis reveals that the order \alpha_s^2 contributions to FL(x,Q2)F_L(x,Q^2) are large whereas these contributions to FT(x,Q2)F_T(x,Q^2) are small. From the above fragmentation functions one can also compute the integrated cross sections σL\sigma_L and σT\sigma_T in an independent way. The sum σtot=σL+σT\sigma_{tot} = \sigma_L + \sigma_T, corrected up to order \alphastwo, agrees with the well known result in the literature providing us with an independent check an our calculations.Comment: 69 pages, latex2e, uses mcite, amsfonts. PostScript version available at http://rulgm4.leidenuniv.nl/preprints/transfrag.p

    Correlated sampling in quantum Monte Carlo: a route to forces

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    In order to find the equilibrium geometries of molecules and solids and to perform ab initio molecular dynamics, it is necessary to calculate the forces on the nuclei. We present a correlated sampling method to efficiently calculate numerical forces and potential energy surfaces in diffusion Monte Carlo. It employs a novel coordinate transformation, earlier used in variational Monte Carlo, to greatly reduce the statistical error. Results are presented for first-row diatomic molecules.Comment: 5 pages, 2 postscript figure

    Nitrogen Retention in Headwater Streams: The Influence of Groundwater-Surface Water Exchange

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    Groundwater-surface water (GW-SW) interaction lengthens hydraulic residence times, increases contact between solutes and biologically active surfaces, and often creates a gradient of redox conditions conducive to an array of biogeochemical processes. As such, the interaction of hydraulic patterns and biogeochemical activity is suspected to be an important determinant of elemental spiraling in streams. Hydrologic interactions may be particularly important in headwater streams, where the extent of the GW-SW mixing environment (i.e., hyporheic zone) is proportionately greater than in larger streams. From our current understanding of stream ecosystem function, we discuss nitrogen (N) spiraling, present a conceptual model of N retention in streams, and use both of these issues to generate specific research questions and testable hypotheses regarding N dynamics in streams

    Can forest management based on natural disturbances maintain ecological resilience?

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    Given the increasingly global stresses on forests, many ecologists argue that managers must maintain ecological resilience: the capacity of ecosystems to absorb disturbances without undergoing fundamental change. In this review we ask: Can the emerging paradigm of natural-disturbance-based management (NDBM) maintain ecological resilience in managed forests? Applying resilience theory requires careful articulation of the ecosystem state under consideration, the disturbances and stresses that affect the persistence of possible alternative states, and the spatial and temporal scales of management relevance. Implementing NDBM while maintaining resilience means recognizing that (i) biodiversity is important for long-term ecosystem persistence, (ii) natural disturbances play a critical role as a generator of structural and compositional heterogeneity at multiple scales, and (iii) traditional management tends to produce forests more homogeneous than those disturbed naturally and increases the likelihood of unexpected catastrophic change by constraining variation of key environmental processes. NDBM may maintain resilience if silvicultural strategies retain the structures and processes that perpetuate desired states while reducing those that enhance resilience of undesirable states. Such strategies require an understanding of harvesting impacts on slow ecosystem processes, such as seed-bank or nutrient dynamics, which in the long term can lead to ecological surprises by altering the forest's capacity to reorganize after disturbance

    Harnessing plant biomass for biofuels and biomaterials

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/72519/1/j.1365-313X.2008.03512.x.pd

    Search for the Proton Decay Mode proton to neutrino K+ in Soudan 2

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    We have searched for the proton decay mode proton to neutrino K+ using the one-kiloton Soudan 2 high resolution calorimeter. Contained events obtained from a 3.56 kiloton-year fiducial exposure through June 1997 are examined for occurrence of a visible K+ track which decays at rest into mu+ nu or pi+ pi0. We found one candidate event consistent with background, yielding a limit, tau/B > 4.3 10^{31} years at 90% CL with no background subtraction.Comment: 13 pages, Latex, 3 tables and 3 figures, Accepted by Physics Letters

    Magnetic ground state of the two isostructual polymeric quantum magnets [Cu(HF2)(pyrazine)2]SbF6 and [Co(HF2)(pyrazine)2]SbF6 investigated with neutron powder diffraction

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    The magnetic ground state of two isostructural coordination polymers, (i) the quasi-two-dimensional S=1/2 square-lattice antiferromagnet [Cu(HF2)(pyrazine)2]SbF6 and (ii) a related compound [Co(HF2)(pyrazine)2]SbF6, was examined with neutron powder diffraction measurements. We find that the ordered moments of the Heisenberg S=1/2 Cu(II) ions in [Cu(HF2)(pyrazine)2]SbF6 are 0.6(1)μb, while the ordered moments for the Co(II) ions in [Co(HF2)(pyrazine)2]SbF6 are 3.02(6)μb. For Cu(II), this reduced moment indicates the presence of quantum fluctuations below the ordering temperature. We show from heat capacity and electron spin resonance measurements that due to the crystal electric field splitting of the S=3/2 Co(II) ions in [Co(HF2)(pyrazine)2]SbF6, this isostructual polymer also behaves as an effective spin-half magnet at low temperatures. The Co moments in [Co(HF2)(pyrazine)2]SbF6 show strong easy-axis anisotropy, neutron diffraction data, which do not support the presence of quantum fluctuations in the ground state, and heat capacity data, which are consistent with 2D or close to 3D spatial exchange anisotropy
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