21 research outputs found

    The Physical Nature of Rest-UV Galaxy Morphology During the Peak Epoch of Galaxy Formation

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    Motivated by the irregular and little-understood morphologies of z ~ 2 - 3 galaxies, we use non-parametric coefficents to quantify the morphologies of 216 galaxies which have been spectroscopically confirmed to lie at redshifts z = 1.8 - 3.4 in the GOODS-N field. Using measurements of ultraviolet (UV) and optical spectral lines, multi-band photometric data, and stellar population models we statistically assess possible correlations between galaxy morphology and physical observables such as stellar mass, star formation rate, and the strength of galaxy-scale outflows. We find evidence that dustier galaxies have more nebulous UV morphologies and that larger, more luminous galaxies may drive stronger outflows, but otherwise conclude that UV morphology is either statistically decoupled from the majority of physical observables or determined by too complex a combination of physical processes to provide characterizations with predictive power. Given the absence of strong correlations between UV morphology and physical parameters such as star formation rates, we are therefore unable to support the hypothesis that morphologically irregular galaxies predominantly represent major galaxy mergers. Comparing galaxy samples, we find that IR-selected BzK galaxies and radio-selected submillimeter galaxies (SMGs) have UV morphologies similar to the optically selected sample, while distant red galaxies (DRGs) are more nebulous.Comment: 26 pages. Accepted for publication in the ApJ. Version with full resolution figures is available at http://www.astro.caltech.edu/~drlaw/Papers/UVmorph.pd

    Speciation of common Gram-negative pathogens using a highly multiplexed high resolution melt curve assay

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    The identification of the bacterial species responsible for an infection remains an important step for the selection of antimicrobial therapy. Gram-negative bacteria are an important source of hospital and community acquired infections and frequently antimicrobial resistant. Speciation of bacteria is typically carried out by biochemical profiling of organisms isolated from clinical specimens, which is time consuming and delays the initiation of tailored treatment. Whilst molecular methods such as PCR have been used, they often struggle with the challenge of detecting and discriminating a wide range of targets. High resolution melt analysis is an end-point qPCR detection method that provides greater multiplexing capability than probe based methods. Here we report the design of a high resolution melt analysis assay for the identification of six common Gram-negative pathogens; Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Pseudomonas aeruginosa, Salmonella Sp, and Acinetobacter baumannii, and a generic Gram-negative specific 16S rRNA control. The assay was evaluated using a well characterised collection of 113 clinically isolated Gram-negative bacteria. The agreement between the HRM assay and the reference test of PCR and sequencing was 98.2% (Kappa 0.96); the overall sensitivity and specificity of the assay was 97.1% (95% CI: 90.1–99.7%) and 100% (95% CI: 91.78–100%) respectively
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