128 research outputs found
Where I Live (2nd grade)
Students will learn utilization of maps and their elements. They will also learn about physical and human characteristics of communities. The goal of this unit is to help students understand that maps tell the story of a community and that people modify their physical environment to meet their needs. Through station exploration, map reading practice, creating digital maps, and exploring the local neighborhood, students with a variety of learning modalities will internalize the purpose of maps. Students transfer their knowledge and skills at the end of the unit by designing a community and creating a map to represent that community
Topological defect motifs in two-dimensional Coulomb clusters
The most energetically favourable arrangement of low-density electrons in an
infinite two-dimensional plane is the ordered triangular Wigner lattice.
However, in most instances of contemporary interest one deals instead with
finite clusters of strongly interacting particles localized in potential traps,
for example, in complex plasmas. In the current contribution we study
distribution of topological defects in two-dimensional Coulomb clusters with
parabolic lateral confinement. The minima hopping algorithm based on molecular
dynamics is used to efficiently locate the ground- and low-energy metastable
states, and their structure is analyzed by means of the Delaunay triangulation.
The size, structure and distribution of geometry-induced lattice imperfections
strongly depends on the system size and the energetic state. Besides isolated
disclinations and dislocations, classification of defect motifs includes defect
compounds --- grain boundaries, rosette defects, vacancies and interstitial
particles. Proliferation of defects in metastable configurations destroys the
orientational order of the Wigner lattice.Comment: 14 pages, 8 figures. This is an author-created, un-copyedited version
of an article accepted for publication in J. Phys.: Condens. Matter. IOP
Publishing Ltd is not responsible for any errors or omissions in this version
of the manuscript or any version derived from it. The definitive
publisher-authenticated version is available online at
10.1088/0953-8984/23/38/38530
Benchmarking implementations of functional languages with âPseudoknot', a float-intensive benchmark
Over 25 implementations of different functional languages are benchmarked using the same program, a floating-point intensive application taken from molecular biology. The principal aspects studied are compile time and execution time for the various implementations that were benchmarked. An important consideration is how the program can be modified and tuned to obtain maximal performance on each language implementation. With few exceptions, the compilers take a significant amount of time to compile this program, though most compilers were faster than the then current GNU C compiler (GCC version 2.5.8). Compilers that generate C or Lisp are often slower than those that generate native code directly: the cost of compiling the intermediate form is normally a large fraction of the total compilation time. There is no clear distinction between the runtime performance of eager and lazy implementations when appropriate annotations are used: lazy implementations have clearly come of age when it comes to implementing largely strict applications, such as the Pseudoknot program. The speed of C can be approached by some implementations, but to achieve this performance, special measures such as strictness annotations are required by non-strict implementations. The benchmark results have to be interpreted with care. Firstly, a benchmark based on a single program cannot cover a wide spectrum of âtypical' applications. Secondly, the compilers vary in the kind and level of optimisations offered, so the effort required to obtain an optimal version of the program is similarly varie
Analysis of the cell surface layer ultrastructure of the oral pathogen Tannerella forsythia
The Gram-negative oral pathogen Tannerella forsythia is decorated with a 2D crystalline surface (S-) layer, with two different S-layer glycoprotein species being present. Prompted by the predicted virulence potential of the S-layer, this study focused on the analysis of the arrangement of the individual S-layer glycoproteins by a combination of microscopic, genetic, and biochemical analyses. The two S-layer genes are transcribed into mRNA and expressed into protein in equal amounts. The S-layer was investigated on intact bacterial cells by transmission electron microscopy, by immune fluorescence microscopy, and by atomic force microscopy. The analyses of wild-type cells revealed a distinct square S-layer lattice with an overall lattice constant of 10.1 ± 0.7 nm. In contrast, a blurred lattice with a lattice constant of 9.0 nm was found on S-layer single-mutant cells. This together with in vitro self-assembly studies using purified (glyco)protein species indicated their increased structural flexibility after self-assembly and/or impaired self-assembly capability. In conjunction with TEM analyses of thin-sectioned cells, this study demonstrates the unusual case that two S-layer glycoproteins are co-assembled into a single S-layer. Additionally, flagella and pilus-like structures were observed on T. forsythia cells, which might impact the pathogenicity of this bacterium
Reversal of Cocaine-Conditioned Place Preference through Methyl Supplementation in Mice: Altering Global DNA Methylation in the Prefrontal Cortex
Analysis of global methylation in cells has revealed correlations between overall DNA methylation status and some biological states. Recent studies suggest that epigenetic regulation through DNA methylation could be responsible for neuroadaptations induced by addictive drugs. However, there is no investigation to determine global DNA methylation status following repeated exposure to addictive drugs. Using mice conditioned place preference (CPP) procedure, we measured global DNA methylation level in the nucleus accumbens (NAc) and the prefrontal cortex (PFC) associated with drug rewarding effects. We found that cocaine-, but not morphine- or food-CPP training decreased global DNA methylation in the PFC. Chronic treatment with methionine, a methyl donor, for 25 consecutive days prior to and during CPP training inhibited the establishment of cocaine, but not morphine or food CPP. We also found that both mRNA and protein level of DNMT (DNA methytransferase) 3b in the PFC were downregulated following the establishment of cocaine CPP, and the downregulation could be reversed by repeated administration of methionine. Our study indicates a crucial role of global PFC DNA hypomethylation in the rewarding effects of cocaine. Reversal of global DNA hypomethylation could significantly attenuate the rewarding effects induced by cocaine. Our results suggest that methionine may have become a potential therapeutic target to treat cocaine addiction
Benchmarking implementations of functional languages with âPseudoknotâ, a float-intensive benchmark
L'action du dibromosuccinate d'éthyle, du monobromomaléate (on fumarate) d'éthyle et dn tartrate d'éthyle sur de l'éthylate de potasse
Permeability and charge-dependent adsorption properties of the S-layer lattice from Bacillus coagulans E38-66.
We investigated the permeability properties of the oblique S-layer lattice from Bacillus coagulans E38-66 after depositing cell wall fragments on a microfiltration membrane, cross-linking the S-layer protein with glutaraldehyde, and degrading the peptidoglycan with lysozyme. Comparative permeability studies on such multilayered S-layer membranes and suspended S-layer vesicles from thermophilic members of the family Bacillaceae with use of the space technique (M. SĂĄra and U. B. Sleytr, J. Bacteriol. 169:4092-4098, 1987) revealed identical molecular exclusion limits (M. SĂĄra and U. B. Sleytr, J. Membr. Sci. 33:27-49, 1987). Examination of the S-layer lattice from B. coagulans E38-66 with the S-layer membrane technique revealed unhindered passage for molecules up to the size of myoglobin (M(r) 17,000). The molecular dimensions of this protein (2.8 by 3.2 by 4.5 nm) correspond approximately to the size of the ovoid-shaped pore previously shown by high-resolution electron microscopy of negatively stained S-layer self-assembly products (D. Pum, M. SĂĄra, and U. B. Sleytr, J. Bacteriol. 171:5296-5303, 1989). Chemical modification of the S-layer protein and comparative labeling, adsorption, and permeability studies clearly demonstrated that (i) in the native state, free amino and carboxyl groups are present on the outer S-layer face and in the interior of the pores and (ii) electrostatic interactions between these groups prevent unspecific adsorption of the S-layer in vivo
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