5,117 research outputs found
NOTES ON THE SYSTEMATY OF SOLOMON ISLANDS' PLANTS AND SOME OF THEIR NEW GUINEA RELATIVES. XI
Preliminary to a revision of the Myrsinaceae of the British Solomon Islands, we have found it necessary to name and validate the two large undescribed species of Tapeinosperma Hook.f., diagnoses of which are given in this paper, in order that their names may be available for use in connection with studies of the phytogeography of the Solomon Islands
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X-ray K-edge analysis of drain lines in Wilhelm Hall, Ames Laboratory
From August 12--27, 1998 X-ray K-edge measurements were made on drain lines in seven rooms in Wilhelm Hall, Ames Laboratory. The purpose of these measurements was to determine the extent of thorium (and other heavy metal) contamination inside these pipes. The K-edge method is a noninvasive inspection technique that can provide accurate quantification of heavy metal contamination interior to an object. Of the seven drain lines inspected, one was found to have no significant contamination, three showed significant thorium deposits, two showed mercury contamination, and one line was found to contain mercury, thorium and uranium. The K-edge measurements were found to be consistent with readings from hand-held survey meters, and provided much greater detail on the location and amount of heavy metal contamination
Variação demográfica causada por exploração florestal no banco de mudas de espécies florestais em resposta a diferentes tamanhos de aberturas no dossel da floresta.
bitstream/item/57644/1/CPATU-PA170.pd
Banco de sementes de floresta tropical úmida no município de Moju, PA.
bitstream/item/57772/1/CPATU-PA185.pd
The UVES Large Program for testing fundamental physics - III. Constraints on the fine-structure constant from 3 telescopes
Large statistical samples of quasar spectra have previously indicated
possible cosmological variations in the fine-structure constant, . A
smaller sample of higher signal-to-noise ratio spectra, with dedicated
calibration, would allow a detailed test of this evidence. Towards that end, we
observed equatorial quasar HS 15491919 with three telescopes: the Very Large
Telescope, Keck and, for the first time in such analyses, Subaru. By directly
comparing these spectra to each other, and by `supercalibrating' them using
asteroid and iodine-cell tests, we detected and removed long-range distortions
of the quasar spectra's wavelength scales which would have caused significant
systematic errors in our measurements. For each telescope we measure
the relative deviation in from the current laboratory value,
, in 3 absorption systems at redshifts
, 1.342, and 1.802. The nine measurements of
are all consistent with zero at the 2- level,
with 1- statistical (systematic) uncertainties 5.6--24 (1.8--7.0) parts
per million (ppm). They are also consistent with each other at the 1-
level, allowing us to form a combined value for each telescope and, finally, a
single value for this line of sight: ppm, consistent with both zero and
previous, large samples. We also average all Large Programme results measuring
ppm.
Our results demonstrate the robustness and reliability at the 3 ppm level
afforded by supercalibration techniques and direct comparison of spectra from
different telescopes.Comment: 24 pages, 11 figures, 9 table
Using H-alpha Morphology and Surface Brightness Fluctuations to Age-Date Star Clusters in M83
We use new WFC3 observations of the nearby grand design spiral galaxy M83 to
develop two independent methods for estimating the ages of young star clusters.
The first method uses the physical extent and morphology of Halpha emission to
estimate the ages of clusters younger than tau ~10 Myr. It is based on the
simple premise that the gas in very young (tau < few Myr) clusters is largely
coincident with the cluster stars, is in a small, ring-like structure
surrounding the stars in slightly older clusters (e.g., tau ~5 Myr), and is in
a larger ring-like bubble for still older clusters (i.e., ~5-10 Myr). The
second method is based on an observed relation between pixel-to-pixel flux
variations within clusters and their ages. This method relies on the fact that
the brightest individual stars in a cluster are most prominent at ages around
10 Myr, and fall below the detection limit (i.e., M_V < -3.5) for ages older
than about 100 Myr. These two methods are the basis for a new morphological
classification system which can be used to estimate the ages of star clusters
based on their appearance. We compare previous age estimates of clusters in M83
determined from fitting UBVI Halpha measurements using predictions from stellar
evolutionary models with our new morphological categories and find good
agreement at the ~95% level. The scatter within categories is ~0.1 dex in log
tau for young clusters (10 Myr) clusters. A
by-product of this study is the identification of 22 "single-star" HII regions
in M83, with central stars having ages ~4 Myr.Comment: 33 pages, 10 figures, 3 tables; published in March Ap
Hubble Space Telescope Images of Stephan's Quintet: Star Cluster Formation in a Compact Group Environment
Analysis of Hubble Space Telescope/Wide Field Planetary Camera 2 images of
Stephan's Quintet, Hickson Compact Group 92, yielded 115 candidate star
clusters (with V-I < 1.5). Unlike in merger remants, the cluster candidates in
Stephan's Quintet are not clustered in the inner regions of the galaxies; they
are spread over the debris and surrounding area. Specifically, these sources
are located in the long sweeping tail and spiral arms of NGC 7319, in the tidal
debris of NGC 7318B/A, and in the intragroup starburst region north of these
galaxies. Analysis of the colors of the clusters indicates several distinct
epochs of star formation that appear to trace the complex history of dynamical
interactions in this compact group.Comment: 24 pages, 21 figures (13 PostScript and 8 JPEG), LaTeX (uses
aastexug.sty), accepted for publication in the Astronomical Journal (July
2001). Full-resolution PostScript figures available at
http://www.astro.psu.edu/users/gallsc/sq/figs.tar.g
Mannose binding lectin is required for alphavirus-induced arthritis/myositis
Mosquito-borne alphaviruses such as chikungunya virus and Ross River virus (RRV) are emerging pathogens capable of causing large-scale epidemics of virus-induced arthritis and myositis. The pathology of RRV-induced disease in both humans and mice is associated with induction of the host inflammatory response within the muscle and joints, and prior studies have demonstrated that the host complement system contributes to development of disease. In this study, we have used a mouse model of RRV-induced disease to identify and characterize which complement activation pathways mediate disease progression after infection, and we have identified the mannose binding lectin (MBL) pathway, but not the classical or alternative complement activation pathways, as essential for development of RRV-induced disease. MBL deposition was enhanced in RRV infected muscle tissue from wild type mice and RRV infected MBL deficient mice exhibited reduced disease, tissue damage, and complement deposition compared to wild-type mice. In contrast, mice deficient for key components of the classical or alternative complement activation pathways still developed severe RRV-induced disease. Further characterization of MBL deficient mice demonstrated that similar to C3(-/-) mice, viral replication and inflammatory cell recruitment were equivalent to wild type animals, suggesting that RRV-mediated induction of complement dependent immune pathology is largely MBL dependent. Consistent with these findings, human patients diagnosed with RRV disease had elevated serum MBL levels compared to healthy controls, and MBL levels in the serum and synovial fluid correlated with severity of disease. These findings demonstrate a role for MBL in promoting RRV-induced disease in both mice and humans and suggest that the MBL pathway of complement activation may be an effective target for therapeutic intervention for humans suffering from RRV-induced arthritis and myositis.This work was supported by NIH/NIAMS R01 AR 047190 awarded to MTH
Germline DNA Repair Gene Mutations in Young-onset Prostate Cancer Cases in the UK: Evidence for a More Extensive Genetic Panel
Background
Rare germline mutations in DNA repair genes are associated with prostate cancer (PCa) predisposition and prognosis.
Objective
To quantify the frequency of germline DNA repair gene mutations in UK PCa cases and controls, in order to more comprehensively evaluate the contribution of individual genes to overall PCa risk and likelihood of aggressive disease.
Design, setting, and participants
We sequenced 167 DNA repair and eight PCa candidate genes in a UK-based cohort of 1281 young-onset PCa cases (diagnosed at ≤60 yr) and 1160 selected controls.
Outcome measurements and statistical analysis
Gene-level SKAT-O and gene-set adaptive combination of p values (ADA) analyses were performed separately for cases versus controls, and aggressive (Gleason score ≥8, n = 201) versus nonaggressive (Gleason score ≤7, n = 1048) cases.
Results and limitations
We identified 233 unique protein truncating variants (PTVs) with minor allele frequency <0.5% in controls in 97 genes. The total proportion of PTV carriers was higher in cases than in controls (15% vs 12%, odds ratio [OR] = 1.29, 95% confidence interval [CI] 1.01–1.64, p = 0.036). Gene-level analyses selected NBN (pSKAT-O = 2.4 × 10−4) for overall risk and XPC (pSKAT-O = 1.6 × 10−4) for aggressive disease, both at candidate-level significance (p < 3.1 × 10−4 and p < 3.4 × 10−4, respectively). Gene-set analysis identified a subset of 20 genes associated with increased PCa risk (OR = 3.2, 95% CI 2.1–4.8, pADA = 4.1 × 10−3) and four genes that increased risk of aggressive disease (OR = 11.2, 95% CI 4.6–27.7, pADA = 5.6 × 10−3), three of which overlap the predisposition gene set.
Conclusions
The union of the gene-level and gene-set-level analyses identified 23 unique DNA repair genes associated with PCa predisposition or risk of aggressive disease. These findings will help facilitate the development of a PCa-specific sequencing panel with both predictive and prognostic potential.
Patient summary
This large sequencing study assessed the rate of inherited DNA repair gene mutations between prostate cancer patients and disease-free men. A panel of 23 genes was identified, which may improve risk prediction or treatment pathways in future clinical practice
Star cluster survival and compressive tides in Antennae-like mergers
Gravitational tides are widely understood to strip and destroy galactic
substructures. In the course of a galaxy merger, however, transient totally
compressive tides may develop and prevent star forming regions from dissolving,
after they condensed to form clusters of stars. We study the statistics of such
compressive modes in an N-body model of the galaxy merger NGC 4038/39 (the
Antennae) and show that ~15% of the disc material undergoes compressive tides
at pericentre. The spatial distribution of observed young clusters in the
overlap and nuclear regions of the Antennae matches surprisingly well the
location of compressive tides obtained from simulation data. Furthermore, the
statistics of time intervals spent by individual particles embedded in a
compressive tide yields a log-normal distribution of characteristic time ~10
Myr, comparable to star cluster formation timescales. We argue that this
generic process is operative in galaxy mergers at all redshifts and possibly
enhances the formation of star clusters. We show with a model calculation that
this process will prevent the dissolution of a star cluster during the
formation phase, even for a star formation efficiency as low as ~10%. The
transient nature of compressive tides implies that clusters may dissolve
rapidly once the tidal field switches to the usual disruptive mode.Comment: 5 pages, 3 figures, accepted for publication in MNRAS Letters. For
higher resolution, see http://astro.u-strasbg.fr/~renaud/publi/mnras08.pd
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