1,139 research outputs found
The Giant Branches of Open and Globular Clusters in the Infrared as Metallicity Indicators: A Comparison with Theory
We apply the giant branch slope-[Fe/H] relation derived by Kuchinski et al.
[AJ, 109, 1131 (1995)] to a sample of open clusters. We find that the slope of
the giant branch in K vs. (J-K) color-magnitude diagrams correlates with [Fe/H]
for open clusters as it does for metal-rich globular clusters but that the open
cluster data are systematically shifted to less negative values of giant branch
slope, at constant [Fe/H]. We use isochrone models to examine the theoretical
basis for this relationship and find that for a given value of [Fe/H], the
slope of the relationship remains constant with decreasing population age but
the relation shifts to less negative values of giant branch slope with
decreasing age. Both of these theoretical predictions agree with the trends
found in the data. Finally, we derive new coefficients for the giant branch
slope-[Fe/H] relation for specific members of 3 populations, metal-rich
globular clusters, bulge stars and open clusters.Comment: 16 pages including 3 figures (AASTEX), AJ Accepted, also available at
http://www.astronomy.ohio-state.edu/~martini/pubs.htm
Uncertainties of size measurements in electron microscopy characterization of nanomaterials in foods
Electron microscopy is a recognized standard tool for nanomaterial characterization, and recommended by the European Food Safety Authority for the size measurement of nanomaterials in food. Despite this, little data have been published assessing the reliability of the method, especially for size measurement of nanomaterials characterized by a broad size distribution and/or added to food matrices. This study is a thorough investigation of the measurement uncertainty when applying electron microscopy for size measurement of engineered nanomaterials in foods. Our results show that the number of measured particles was only a minor source of measurement uncertainty for nanomaterials in food, compared to the combined influence of sampling, sample preparation prior to imaging and the image analysis. The main conclusion is that to improve the measurement reliability, care should be taken to consider replications and matrix removal prior to sample preparation
The Metallicity and Reddening of Stars in the Inner Galactic Bulge
We present a preliminary analysis of K, J-K color magnitude diagrams (CMDs)
for 7 different positions on or close to the minor axis of the Milky Way at
Galactic latitudes between +0.1^\circ and -2.8^\circ. From the slopes of the
(linear) giant branches in these CMDs we derive a dependence of on
latitude for b between -0.8^\circ and -2.8^\circ of -0.085 \pm 0.033
dex/degree. When combined with the data from Tiede et al. we find for
-0.8^\circ \leq b \leq -10.3^\circ the slope in is -0.064 \pm 0.012
dex/degree. An extrapolation to the Galactic Center predicts [Fe/H] = +0.034
\pm 0.053 dex. We also derive average values for the extinction in the K band
(A_K) of between 2.15 and 0.27 for the inner bulge fields corresponding to
average values of E(J-K) of between 3.46 and 0.44. There is a well defined
linear relation between the average extinction for a field and the star-to-star
scatter in the extinction for the stars within each field. This result suggests
that the typical apparent angular scale size for an absorbing cloud is small
compared with the field size (90\arcsec on a side). Finally, from an
examination of the luminosity function of bright giants in each field we
conclude that the young component of the stellar population observed near the
Galactic center declines in density much more quickly than the overall bulge
population and is undetectable beyond 1^\circ from the Galactic center.Comment: accepted for publication in Astron. Jour. Compressed file contains
the text, 9 figures, and 6 tables prepared with AAS Latex macros v. 4.
Genome-Wide Association Study and Pathway-Level Analysis of Kernel Color in Maize.
Rapid development and adoption of biofortified, provitamin A-dense orange maize (Zea mays L.) varieties could be facilitated by a greater understanding of the natural variation underlying kernel color, including as it relates to carotenoid biosynthesis and retention in maize grain. Greater abundance of carotenoids in maize kernels is generally accompanied by deeper orange color, useful for distinguishing provitamin A-dense varieties to consumers. While kernel color can be scored and selected with high-throughput, low-cost phenotypic methods within breeding selection programs, it remains to be well established as to what would be the logical genetic loci to target for selection for kernel color. We conducted a genome-wide association study of maize kernel color, as determined by colorimetry, in 1,651 yellow and orange inbreds from the Ames maize inbred panel. Associations were found with y1, encoding the first committed step in carotenoid biosynthesis, and with dxs2, which encodes the enzyme responsible for the first committed step in the biosynthesis of the isoprenoid precursors of carotenoids. These genes logically could contribute to overall carotenoid abundance and thus kernel color. The lcyE and zep1 genes, which can affect carotenoid composition, were also found to be associated with colorimeter values. A pathway-level analysis, focused on genes with a priori evidence of involvement in carotenoid biosynthesis and retention, revealed associations for dxs3 and dmes1, involved in isoprenoid biosynthesis; ps1 and vp5, within the core carotenoid pathway; and vp14, involved in cleavage of carotenoids. Collectively, these identified genes appear relevant to the accumulation of kernel color
Implications of New JHK Photometry and a Deep Infrared Luminosity Function for the Galactic Bulge
We present deep near-IR photometry for Galactic bulge stars in Baade's
Window, and another minor axis field at . We combine our data with previously published photometry
and construct a luminosity function over the range ,
deeper than any previously published. The slope of this luminosity function and
the magnitude of the tip of the first ascent giant branch are consistent with
theoretical values derived from isochrones with appropriate age and
metallicity.
We use the relationship between [Fe/H] and the giant branch slope derived
from near-IR observations of metal rich globular clusters by Kuchinski {\it et
al.} [AJ, 109, 1131 (1995)] to calculate the mean metallicity for several bulge
fields along the minor axis. For Baade's Window we derive , consistent with the recent estimate of
McWilliam \& Rich [ApJS, 91, 749 (1994)], but somewhat lower than previous
estimates based on CO and TiO absorption bands and the colors of M giants
by Frogel {\it et al.} [ApJ, 353, 494 (1990)]. Between and
we find a gradient in of dex/degree or dex/kpc for kpc, consistent with
other independent derivations. We derive a helium abundance for Baade's Window
with the and methods and find that implying
.
Next, we find that the bolometric corrections for bulge K giants () are in excellent agreement with empirical derivations based on observations
of globular cluster and local field stars. However, for the redder M giants weComment: Accepted by the Astronomical Journal. 43 pages, uuencoded compressed
PostScript, no figures or tables. A complete (text, figs and tables) preprint
is also available at
ftp://bessel.mps.ohio-state.edu/pub/terndrup/bwphot.tar.Z (compressed tar
file with PostScript
Distances to Populous Clusters in the LMC via the K-Band Luminosity of the Red Clump
We present results from a study of the distances and distribution of a sample
of intermediate-age clusters in the Large Magellanic Cloud. Using deep
near-infrared photometry obtained with ISPI on the CTIO 4m, we have measured
the apparent K-band magnitude of the core helium burning red clump stars in 17
LMC clusters. We combine cluster ages and metallicities with the work of
Grocholski & Sarajedini to predict each cluster's absolute K-band red clump
magnitude, and thereby calculate absolute cluster distances. An analysis of
these data shows that the cluster distribution is in good agreement with the
thick, inclined disk geometry of the LMC, as defined by its field stars. We
also find that the old globular clusters follow the same distribution,
suggesting that the LMC's disk formed at about the same time as the globular
clusters, ~ 13 Gyr ago. Finally, we have used our cluster distances in
conjunction with the disk geometry to calculate the distance to the LMC center,
for which we find (m-M)o = 18.40 +/- 0.04_{ran} +/- 0.08_{sys}, or Do = 47.9
+/- 0.9 +/- 1.8 kpc.Comment: 31 pages including 5 figures and 7 tables. Accepted for publication
in the August 2007 issue of A
Novel parameters for evaluating the Spatial and Thematic accuracy of land cover maps.
Se proponen novedosas fórmulas para evaluar la certeza de la cartografí
Live Imaging of Type I Collagen Assembly Dynamics in Osteoblasts Stably Expressing GFP and mCherry-Tagged Collagen Constructs
Type I collagen is the most abundant extracellular matrix protein in bone and other connective tissues and plays key roles in normal and pathological bone formation as well as in connective tissue disorders and fibrosis. Although much is known about the collagen biosynthetic pathway and its regulatory steps, the mechanisms by which it is assembled extracellularly are less clear. We have generated GFPtpz and mCherry-tagged collagen fusion constructs for live imaging of type I collagen assembly by replacing the α2(I)-procollagen N-terminal propeptide with GFPtpz or mCherry. These novel imaging probes were stably transfected into MLO-A5 osteoblast-like cells and fibronectin-null mouse embryonic fibroblasts (FN-null-MEFs) and used for imaging type I collagen assembly dynamics and its dependence on fibronectin. Both fusion proteins co-precipitated with α1(I)-collagen and remained intracellular without ascorbate but were assembled into α1(I) collagen-containing extracellular fibrils in the presence of ascorbate. Immunogold-EM confirmed their ultrastuctural localization in banded collagen fibrils. Live cell imaging in stably transfected MLO-A5 cells revealed the highly dynamic nature of collagen assembly and showed that during assembly the fibril networks are continually stretched and contracted due to the underlying cell motion. We also observed that cell-generated forces can physically reshape the collagen fibrils. Using co-cultures of mCherry- and GFPtpz-collagen expressing cells, we show that multiple cells contribute collagen to form collagen fiber bundles. Immuno-EM further showed that individual collagen fibrils can receive contributions of collagen from more than one cell. Live cell imaging in FN-null-MEFs expressing GFPtpz-collagen showed that collagen assembly was both dependent upon and dynamically integrated with fibronectin assembly. These GFP-collagen fusion constructs provide a powerful tool for imaging collagen in living cells and have revealed novel and fundamental insights into the dynamic mechanisms for the extracellular assembly of collagen
β1 Integrin Signaling Maintains Human Epithelial Progenitor Cell Survival In Situ and Controls Proliferation, Apoptosis and Migration of Their Progeny
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