Basic Bible Interpretation: Introducing the Inductive Bible Study Method

There is a dire need for Christians to know a viable method of biblical interpretation. This project seeks to address that need through teaching the inductive Bible study to a group of people in a Southern Baptist congregation. The participant learning outcomes for the project were to acquire a method of biblical interpretation, develop the ability to perform a method of biblical interpretation, gain knowledge of the book of Jude, and to utilize meditation as a means to enrich spirituality. This project used action research as its primary methodology. The triangulation method of data analysis was employed by collecting data from the pre-test and post-test, focus group, and field notes. A Likert survey was used to determine the likability of the project and to determine if the project could be repeated within the local ministry context. Through the data collected the project seeks to demonstrate that the inductive Bible study method is a viable option for one’s own personal Bible study method

Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA.

Escherichia coli RecA is the defining member of a ubiquitous class of DNA strand-exchange proteins that are essential for homologous recombination, a pathway that maintains genomic integrity by repairing broken DNA. To function, filaments of RecA must nucleate and grow on single-stranded DNA (ssDNA) in direct competition with ssDNA-binding protein (SSB), which rapidly binds and continuously sequesters ssDNA, kinetically blocking RecA assembly. This dynamic self-assembly on a DNA lattice, in competition with another protein, is unique for the RecA family compared to other filament-forming proteins such as actin and tubulin. The complexity of this process has hindered our understanding of RecA filament assembly because ensemble measurements cannot reliably distinguish between the nucleation and growth phases, despite extensive and diverse attempts. Previous single-molecule assays have measured the nucleation and growth of RecA--and its eukaryotic homologue RAD51--on naked double-stranded DNA and ssDNA; however, the template for RecA self-assembly in vivo is SSB-coated ssDNA. Using single-molecule microscopy, here we directly visualize RecA filament assembly on single molecules of SSB-coated ssDNA, simultaneously measuring nucleation and growth. We establish that a dimer of RecA is required for nucleation, followed by growth of the filament through monomer addition, consistent with the finding that nucleation, but not growth, is modulated by nucleotide and magnesium ion cofactors. Filament growth is bidirectional, albeit faster in the 5'→3' direction. Both nucleation and growth are repressed at physiological conditions, highlighting the essential role of recombination mediators in potentiating assembly in vivo. We define a two-step kinetic mechanism in which RecA nucleates on transiently exposed ssDNA during SSB sliding and/or partial dissociation (DNA unwrapping) and then the RecA filament grows. We further demonstrate that the recombination mediator protein pair, RecOR (RecO and RecR), accelerates both RecA nucleation and filament growth, and that the introduction of RecF further stimulates RecA nucleation

Controlling uranyl oxo group interactions to group 14 elements using polypyrrolic Schiff-base macrocyclic ligands

Heterodinuclear uranyl/group 14 complexes of the aryl- and anthracenyl-linked Schiff-base macrocyclic ligands LMe and LA were synthesised by reaction of UO2(H2L) with M{N(SiMe3)2}2 (M = Ge, Sn, Pb). For complexes of the anthracenyl-linked ligand (LA) the group 14 metal sits out of the N4-donor plane by up to 0.7 Å resulting in relatively short M⋯OUO distances which decrease down the group; however, the solid state structures and IR spectroscopic analyses suggest little interaction occurs between the oxo and group 14 metal. In contrast, the smaller aryl-linked ligand (LMe) enforces greater interaction between the metals; only the PbII complex was cleanly accessible although this complex was relatively unstable in the presence of HN(SiMe3)2 and some organic oxidants. In this case, the equatorial coordination of pyridine-N-oxide causes a 0.08 Å elongation of the endo UO bond and a clear interaction of the uranyl ion with the Pb(II) cation in the second donor compartment

Uranyl to Uranium(IV) Conversion through Manipulation of Axial and Equatorial Ligands

The controlled manipulation of the axial oxo and equatorial halide ligands in the uranyl dipyrrin complex, UO2Cl(L), allows the uranyl reduction potential to be shifted by 1.53 V into the range accessible to naturally occurring reductants that are present during uranium remediation and storage processes. Abstraction of the equatorial halide ligand to form the uranyl cation causes a 780 mV positive shift in the UV/UIV reduction potential. Borane functionalization of the axial oxo groups causes the spontaneous homolysis of the equatorial U–Cl bond and a further 750 mV shift of this potential. The combined effect of chloride loss and borane coordination to the oxo groups allows reduction of UVI to UIV by H2 or other very mild reductants such as Cp*2Fe. The reduction with H2 is accompanied by a B–C bond cleavage process in the oxo-coordinated borane

Two objects or one? similarity rather than complexity determines objecthood when resolving dynamic input

The human brain is continuously confronted with dynamic visual input, and from this it must infer whether input belongs to a single versus multiple object identities across time. Object substitution masking (OSM), in which perception of a target stimulus is impaired by a temporally trailing 4-dot mask, reflects a failure to segment the target and mask as discrete objects. According to Bouvier and Treisman (2010), OSM only occurs for targets that require binding multiple separate features (e.g., color and orientation) to be identified. In contrast, a target that represents a unique feature is thought to be impervious to masking. Here, however, we show that a single orientation target (a Gabor) is susceptible to masking with an orientation-discrimination task, but only when the mask is similar in orientation to the target. That is, target-mask similarity, rather than target complexity determines masking. A reexamination of Bouvier and Treisman’s (2010) results show that they can be explained within this target-mask similarity perspective. This means that the similarity of 2 objects determines whether they will be integrated or segmented across time, rather than the complexity of 1 of the objects in isolation.The research was supported by an Australian Research Council grant: arc ID:de140101734

Using ISERV and Commercial Satellite Imagery to Assess and Monitor Recovery Efforts in Urban Damaged Areas

No abstract availabl

Using ISERV and Commercial Satellite Imagery to Assess and Monitor Recovery Efforts in Urban Damaged Areas

No abstract availabl

Development of WMS Capabilities to Support NASA Disasters Applications and App Development

During the last year several significant disasters have occurred such as Superstorm Sandy on the East coast of the United States, and Typhoon Bopha in the Phillipines, along with several others. In support of these disasters NASA's Shortterm Prediction Research and Transition (SPoRT) Center delivered various products derived from satellite imagery to help in the assessment of damage and recovery of the affected areas. To better support the decision makers responding to the disasters SPoRT quickly developed several solutions to provide the data using open Geographical Information Service (GIS) formats. Providing the data in open GIS standard formats allowed the end user to easily integrate the data into existing Decision Support Systems (DSS). Both Tile Mapping Service (TMS) and Web Mapping Service (WMS) were leveraged to quickly provide the data to the enduser. Development of the deliver methodology allowed quick response to rapidly developing disasters and enabled NASA SPoRT to bring science data to decision makers in a successful research to operations transition

Strict detector-efficiency bounds for n-site Clauser-Horne inequalities

An analysis of detector-efficiency in many-site Clauser-Horne inequalities is presented, for the case of perfect visibility. It is shown that there is a violation of the presented n-site Clauser-Horne inequalities if and only if the efficiency is greater than n/(2n-1). Thus, for a two-site two-setting experiment there are no quantum-mechanical predictions that violate local realism unless the efficiency is greater than 2/3. Secondly, there are n-site experiments for which the quantum-mechanical predictions violate local realism whenever the efficiency exceeds 1/2.Comment: revtex, 5 pages, 1 figure (typesetting changes only