639 research outputs found
A taxonomic revision of Mazus lour. (Scrophulariaceae) in Australasia
Mazus is shown to consist of three species in the Australia-New Zealand region. Mazus pumilio R. Br. of past concepts is shown to consist of two species, M. pumilio S.str. being confined to southeastern Australia and a new species, M. novaezeelandiae, to lowland New Zealand; morphological floral differences may reflect different breeding systems, with the former thought to be self-incompatible and the latter self-compatible. Mazus radicans (Hook. f.) Cheeseman is confined to New Zealand and extends to higher altitudes than M. novaezeelandiae. Its flowers may be small and cleistogamous or "bud-autogamous" as well as large and chasmogamous. Distinctions from M. pumilus (Burm. f.) Steenis, a weedy southeast Asian annual extending to a few locations in New Guinea, are given in the key to species
Local adaptation or foreign advantage? Effective use of a single-test site common garden to evaluate adaptation across ecological scales
A Natural Planning Framework: Putting the natural environment at the heart of the National Planning Framework for England.
On the flexibility of the design of Multiple Try Metropolis schemes
The Multiple Try Metropolis (MTM) method is a generalization of the classical
Metropolis-Hastings algorithm in which the next state of the chain is chosen
among a set of samples, according to normalized weights. In the literature,
several extensions have been proposed. In this work, we show and remark upon
the flexibility of the design of MTM-type methods, fulfilling the detailed
balance condition. We discuss several possibilities and show different
numerical results
Three applications of path integrals: equilibrium and kinetic isotope effects, and the temperature dependence of the rate constant of the [1,5] sigmatropic hydrogen shift in (Z)-1,3-pentadiene
Recent experiments have confirmed the importance of nuclear quantum effects
even in large biomolecules at physiological temperature. Here we describe how
the path integral formalism can be used to describe rigorously the nuclear
quantum effects on equilibrium and kinetic properties of molecules.
Specifically, we explain how path integrals can be employed to evaluate the
equilibrium (EIE) and kinetic (KIE) isotope effects, and the temperature
dependence of the rate constant. The methodology is applied to the [1,5]
sigmatropic hydrogen shift in pentadiene. Both the KIE and the temperature
dependence of the rate constant confirm the importance of tunneling and other
nuclear quantum effects as well as of the anharmonicity of the potential energy
surface. Moreover, previous results on the KIE were improved by using a
combination of a high level electronic structure calculation within the
harmonic approximation with a path integral anharmonicity correction using a
lower level method.Comment: 9 pages, 4 figure
Ethnic Variation in Inflammatory Profile in Tuberculosis
PMCID: PMC3701709This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Psychological determinants of whole-body endurance performance
Background: No literature reviews have systematically identified and evaluated research on the psychological determinants of endurance performance, and sport psychology performance-enhancement guidelines for endurance sports are not founded on a systematic appraisal of endurance-specific research.
Objective: A systematic literature review was conducted to identify practical psychological interventions that improve endurance performance and to identify additional psychological factors that affect endurance performance. Additional objectives were to evaluate the research practices of included studies, to suggest theoretical and applied implications, and to guide future research.
Methods: Electronic databases, forward-citation searches, and manual searches of reference lists were used to locate relevant studies. Peer-reviewed studies were included when they chose an experimental or quasi-experimental research design, a psychological manipulation, endurance performance as the dependent variable, and athletes or physically-active, healthy adults as participants.
Results: Consistent support was found for using imagery, self-talk, and goal setting to improve endurance performance, but it is unclear whether learning multiple psychological skills is more beneficial than learning one psychological skill. The results also demonstrated that mental fatigue undermines endurance performance, and verbal encouragement and head-to-head competition can have a beneficial effect. Interventions that influenced perception of effort consistently affected endurance performance.
Conclusions: Psychological skills training could benefit an endurance athlete. Researchers are encouraged to compare different practical psychological interventions, to examine the effects of these interventions for athletes in competition, and to include a placebo control condition or an alternative control treatment. Researchers are also encouraged to explore additional psychological factors that could have a negative effect on endurance performance. Future research should include psychological mediating variables and moderating variables. Implications for theoretical explanations of endurance performance and evidence-based practice are described
I-TRAP: A method to identify transcriptional regulator activated promoters
BACKGROUND: The differential expression of virulence genes is often used by microbial pathogens in adapting to the environment of their host. The differential expression of such sets of genes can be regulated by RNA polymerase sigma factors. Some sigma factors are differentially expressed, which can provide a means to identifying other differentially expressed genes such as those whose expression are controlled by the sigma factor. METHODS: To identify sigma factor-regulated genes, we developed a method, termed I-TRAP, for the identification of transcriptional regulator activated promoters. The I-TRAP method is based on the fact that some genes will be differentially expressed in the presence and absence of a transcriptional regulator. I-TRAP uses a DNA library in a promoter-trap vector that contains two reporter genes, one to allow the selection of active promoters in the presence of the transcriptional regulator and a second to allow screening for promoter activity in the absence of the transcriptional regulator. RESULTS: To illustrate the development and use of the I-TRAP approach, the construction of the vectors, host strains, and library necessary to identify SigmaE-regulated genes of Mycobacterium tuberculosis is described. CONCLUSION: The I-TRAP method should be a versatile and useful method for identifying and characterizing promoter activity under a variety of conditions and in response to various regulatory proteins. In our study, we isolated 360 clones that may contain plasmids carrying SigmaE-regulated promoters genes of M. tuberculosis
TraR, a Homolog of a RNAP Secondary Channel Interactor, Modulates Transcription
Recent structural and biochemical studies have identified a novel control mechanism of gene expression mediated through the secondary channel of RNA Polymerase (RNAP) during transcription initiation. Specifically, the small nucleotide ppGpp, along with DksA, a RNAP secondary channel interacting factor, modifies the kinetics of transcription initiation, resulting in, among other events, down-regulation of ribosomal RNA synthesis and up-regulation of several amino acid biosynthetic and transport genes during nutritional stress. Until now, this mode of regulation of RNAP was primarily associated with ppGpp. Here, we identify TraR, a DksA homolog that mimics ppGpp/DksA effects on RNAP. First, expression of TraR compensates for dksA transcriptional repression and activation activities in vivo. Second, mutagenesis of a conserved amino acid of TraR known to be critical for DksA function abolishes its activity, implying both structural and functional similarity to DksA. Third, unlike DksA, TraR does not require ppGpp for repression of the rrnB P1 promoter in vivo and in vitro or activation of amino acid biosynthesis/transport genes in vivo. Implications for DksA/ppGpp mechanism and roles of TraR in horizontal gene transfer and virulence are discussed
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