Lattice ϕ4\phi^4 theory of finite-size effects above the upper critical dimension

We present a perturbative calculation of finite-size effects near $T_c$ of the $\phi^4$ lattice model in a $d$-dimensional cubic geometry of size $L$ with periodic boundary conditions for $d > 4$. The structural differences between the $\phi^4$ lattice theory and the $\phi^4$ field theory found previously in the spherical limit are shown to exist also for a finite number of components of the order parameter. The two-variable finite-size scaling functions of the field theory are nonuniversal whereas those of the lattice theory are independent of the nonuniversal model parameters.One-loop results for finite-size scaling functions are derived. Their structure disagrees with the single-variable scaling form of the lowest-mode approximation for any finite $\xi/L$ where $\xi$ is the bulk correlation length. At $T_c$, the large-$L$ behavior becomes lowest-mode like for the lattice model but not for the field-theoretic model. Characteristic temperatures close to $T_c$ of the lattice model, such as $T_{max}(L)$ of the maximum of the susceptibility $\chi$, are found to scale asymptotically as $T_c - T_{max}(L) \sim L^{-d/2}$, in agreement with previous Monte Carlo (MC) data for the five-dimensional Ising model. We also predict $\chi_{max} \sim L^{d/2}$ asymptotically. On a quantitative level, the asymptotic amplitudes of this large -$L$ behavior close to $T_c$ have not been observed in previous MC simulations at $d = 5$ because of nonnegligible finite-size terms $\sim L^{(4-d)/2}$ caused by the inhomogeneous modes. These terms identify the possible origin of a significant discrepancy between the lowest-mode approximation and previous MC data. MC data of larger systems would be desirable for testing the magnitude of the $L^{(4-d)/2}$ and $L^{4-d}$ terms predicted by our theory.Comment: Accepted in Int. J. Mod. Phys.

Future capacity growth of energy technologies: are scenarios consistent with historical evidence?

Future scenarios of the energy system under greenhouse gas emission constraints depict dramatic growth in a range of energy technologies. Technological growth dynamics observed historically provide a useful comparator for these future trajectories. We find that historical time series data reveal a consistent relationship between how much a technology’s cumulative installed capacity grows, and how long this growth takes. This relationship between extent (how much) and duration (for how long) is consistent across both energy supply and end-use technologies, and both established and emerging technologies. We then develop and test an approach for using this historical relationship to assess technological trajectories in future scenarios. Our approach for “learning from the past” contributes to the assessment and verification of integrated assessment and energy-economic models used to generate quantitative scenarios. Using data on power generation technologies from two such models, we also find a consistent extent - duration relationship across both technologies and scenarios. This relationship describes future low carbon technological growth in the power sector which appears to be conservative relative to what has been evidenced historically. Specifically, future extents of capacity growth are comparatively low given the lengthy time duration of that growth. We treat this finding with caution due to the low number of data points. Yet it remains counter-intuitive given the extremely rapid growth rates of certain low carbon technologies under stringent emission constraints. We explore possible reasons for the apparent scenario conservatism, and find parametric or structural conservatism in the underlying models to be one possible explanation

Universal scaling behavior at the upper critical dimension of non-equilibrium continuous phase transitions

In this work we analyze the universal scaling functions and the critical exponents at the upper critical dimension of a continuous phase transition. The consideration of the universal scaling behavior yields a decisive check of the value of the upper critical dimension. We apply our method to a non-equilibrium continuous phase transition. But focusing on the equation of state of the phase transition it is easy to extend our analysis to all equilibrium and non-equilibrium phase transitions observed numerically or experimentally.Comment: 4 pages, 3 figure

Comprehensive Organic Analysis of Antartic Micrometeorites

Introduction: Micrometeorites (MMs) are thought to be significant contributors of organic material to the early Earth [1], and a variety of techniques have been employed to identify their organic composition [2-6]. These include the identification of key organic groups using combinations of infrared, energy dispersive Xray, electron energy loss and Raman spectroscopy and scanning transmission X-ray microscopy [2-4], highlighting similarities between that of MMs and carbonaceous chondrites. Few studies, however, have focused on the characterisation of individual micrometeoritic organic components. Microscopic L2MS has been used to identify up to C5 polycyclic aromatic hydrocarbons and their alkyl derivatives [5]. A combination of ionexchange chromatography and fluorimetric detection has also been successful in identifying a number of protein amino acids including glycine and alanine [6]. We have previously reported a method to analyse ?g-sized quantities of extraterrestrial materials, with prior application to assessing organic volatile release from MM atmospheric entry heating simulations [7]. In this study we utilise this technique to characterise the organic composition of Antarctic terrestrial particles and MMs collected in 1994 from Cap-Prudhomme [8]

Structure of purine nucleoside phosphorylase (DeoD) from Bacillus anthracis

Protein structures from the causative agent of anthrax (Bacillus anthracis) are being determined as part of a structural genomics programme. Amongst initial candidates for crystallographic analysis are enzymes involved in nucleotide biosynthesis, since these are recognized as potential targets in antibacterial therapy. Purine nucleoside phosphorylase is a key enzyme in the purine-salvage pathway. The crystal structure of purine nucleoside phosphorylase (DeoD) from B. anthracis has been solved by molecular replacement at 2.24 Å resolution and refined to an R factor of 18.4%. This is the first report of a DeoD structure from a Gram-positive bacterium

Similarity Renormalization, Hamiltonian Flow Equations, and Dyson's Intermediate Representation

A general framework is presented for the renormalization of Hamiltonians via a similarity transformation. Divergences in the similarity flow equations may be handled with dimensional regularization in this approach, and the resulting effective Hamiltonian is finite since states well-separated in energy are uncoupled. Specific schemes developed several years ago by Glazek and Wilson and contemporaneously by Wegner correspond to particular choices within this framework, and the relative merits of such choices are discussed from this vantage point. It is shown that a scheme for the transformation of Hamiltonians introduced by Dyson in the early 1950's also corresponds to a particular choice within the similarity renormalization framework, and it is argued that Dyson's scheme is preferable to the others for ease of computation. As an example, it is shown how a logarithmically confining potential arises simply at second order in light-front QCD within Dyson's scheme, a result found previously for other similarity renormalization schemes. Steps toward higher order and nonperturbative calculations are outlined. In particular, a set of equations analogous to Dyson-Schwinger equations is developed.Comment: REVTex, 32 pages, 7 figures (corrected references

Ground state energy of the modified Nambu-Goto string

We calculate, using zeta function regularization method, semiclassical energy of the Nambu-Goto string supplemented with the boundary, Gauss-Bonnet term in the action and discuss the tachyonic ground state problem.Comment: 10 pages, LaTeX, 2 figure