190 research outputs found
Instrumentation of sampling aircraft for measurement of launch vehicle effluents
An aircraft was selected and instrumented to measure effluents emitted from large solid propellant rockets during launch activities. The considerations involved in aircraft selection, sampling probes, and instrumentation are discussed with respect to obtaining valid airborne measurements. Discussions of the data acquisition system used, the instrument power system, and operational sampling procedures are included. Representative measurements obtained from an actual rocket launch monitoring activity are also presented
Inhibition of Defocus-Induced Myopia in Chickens
Woods, J., Guthrie, S. E., Keir, N., Dillehay, S., Tyson, M., Griffin, R., β¦ Irving, E. (2013). Inhibition of Defocus-Induced Myopia in Chickens. Investigative Opthalmology & Visual Science, 54(4), 2662. https://doi.org/10.1167/iovs.12-10742Purpose.: To determine the effect of wearing a lens with a unique peripheral optical design on the development and progression of defocus-induced myopia in newly hatched chickens.Methods.: Eighty-five newly hatched chickens underwent bilateral retinoscopy and A-scan ultrasound to determine their refractive error and axial length. They were randomly divided into Control and two Test groups, in which each chicken was fitted with a goggle-lens over the right eye, with the left eye remaining untreated. The Control group wore a lens of power β10.00 diopters (D) of standard spherical optical design. The two Test lenses both had a central optical power β10.00 D, but used different peripheral myopia progression control (MPC) designs. For all groups, retinoscopy was repeated on days 3, 7, 10, and 14; ultrasound was repeated on day 14.
Results.: On day 0 there was no statistical difference in refractive error (mean +6.92 D) or axial length (mean 8.06 mm) between Test and Control groups or treated and untreated eyes (all P > 0.05). At day 14, 37 (43.5%) of 85 chickens had not experienced goggle detachment and were included in the final analyses. In this cohort there was a significant refractive difference between the treated eyes of the Control group (n = 17) and those of Test 1 (n = 14) and Test 2 (n = 6) groups (both P < 0.01): Control β4.65 Β± 2.11 D, Test 1 +4.57 Β± 3.11 D, Test 2 +1.08 Β± 1.24 D (mean Β± SEM). There was also a significant axial length difference (both P < 0.01): Control 10.55 Β± 0.36 mm, Test 1 9.99 Β± 0.14 mm, Test 2 10.17 Β± 0.18 mm.
Conclusions.: Use of these unique MPC lens designs over 14 days caused a significant reduction in the development of defocus-induced myopia in chickens; the degree of reduction appeared to be design specific
Age-related differences in neuroinflammatory responses associated with a distinct profile of regulatory markers on neonatal microglia
Macromolecular structure and organization of alpha keratin
The small-angle equatorial X-ray scattering of alpha keratin (African porcupine quill) was studied using a direct type of analysis, which allows the separation of the intermicro-fibrillar interference effects from those of the intramicrofibrillar scattering without the use of prior assumptions. X-ray data were obtained from 470β21 Γ
; their analysis by the above method resulted in a z -axis projection of the microfibrillar electron density, which extends over a diameter of 80 Γ
and has a core region surrounded by a peak located at a radius of 28 Γ
. The macromolecular organization of the 80-Γ
-diameter microfibrils was found to be an arc-like layer type of aggregation and not a pseudohexagonal packing. When the specimen was subjected to silver staining the aggregation of the microfibrils did not change except for a slight contraction. The z -axis projection of the stained microfibril, however, was significantly different. The silver appears to build up slightly around the outer periphery of the microfibril, stains the peripheral region very little, deposits on the inside of the peripheral region, and outlines the core area.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/37835/1/360130203_ftp.pd
A Weak Gravitational Lensing and X-ray Analysis of Abell 2163
We report on the detection of dark matter in the cluster of galaxies
Abell~2163 using the weak gravitational distortion of background galaxies, and
an analysis of the cluster X-ray emission. We find that while the qualitative
distributions of the cluster light and the dark matter are similar -- shallow
and extended, with significant substructure -- the X-ray morphology shows a
more regular overall appearance. We interpret the joint lensing and X-ray
observations as a signature of a merger event in the cluster. We present new
ROSAT/HRI data and reanalyze ROSAT/PSPC data, accounting for the effect of a
varying background to determine the best fit parameters in the -model
formalism. We combine the surface brightness fits with two determinations of
the radial temperature profile to determine the total mass. Although there are
slight variations in the total mass determinations introduced by the
uncertainties in the -fit, the main contributor to the error arises from
the uncertainties in the temperature determinations. Even though the
morphologies of the dark matter/light and X-ray gas are quite different, we
find that the total mass determined from the X-ray and weak lensing estimates
are consistent with each other within the error bars, with the X-ray
inferred mass a factor of larger. However, as the lensing mass
estimates are differential (the surface density at any point is determined
relative to the mean in a control annulus), the shallow, extended nature of the
mass profile biases the lensing inferred mass downwards. We estimate the
correction for this effect and find very good agreement between the corrected
lensing and X-ray results. We determine the gas mass fraction and find at all radii and a constant mass-to-light ratio of $M/L_VComment: 30 pages, latex file. Postscript file also available at
ftp://magicbean.berkeley.edu/pub/squires/a2163/a2163_paper.ps.g
Melioidosis Vaccines: A Systematic Review and Appraisal of the Potential to Exploit Biodefense Vaccines for Public Health Purposes
The designation of Burkholderia pseudomallei as a category B select agent has resulted in considerable research funding to develop a protective vaccine. This bacterium also causes a naturally occurring disease (melioidosis), an important cause of death in many countries including Thailand and Australia. In this study, we explored whether a vaccine could be used to provide protection from melioidosis. An economic evaluation based on its use in Thailand indicated that a vaccine could be a cost-effective intervention if used in high-risk populations such as diabetics and those with chronic kidney or lung disease. A literature search of vaccine studies in animal models identified the current candidates, but noted that models failed to take account of the common routes of infection in natural melioidosis and major risk factors for infection, primarily diabetes. This review highlights important areas for future research if biodefence-driven vaccines are to play a role in reducing the global incidence of melioidosis
Poly-Thymidine Oligonucleotides Mediate Activation of Murine Glial Cells Primarily Through TLR7, Not TLR8
The functional role of murine TLR8 in the inflammatory response of the central nervous system (CNS) remains unclear. Murine TLR8 does not appear to respond to human TLR7/8 agonists, due to a five amino acid deletion in the ectodomain. However, recent studies have suggested that murine TLR8 may be stimulated by alternate ligands, which include vaccinia virus DNA, phosphothioate oligodeoxynucleotides (ODNs) or the combination of phosphothioate poly-thymidine oligonucleotides (pT-ODNs) with TLR7/8 agonists. In the current study, we analyzed the ability of pT-ODNs to induce activation of murine glial cells in the presence or absence of TLR7/8 agonists. We found that TLR7/8 agonists induced the expression of glial cell activation markers and induced the production of multiple proinflammatory cytokines and chemokines in mixed glial cultures. In contrast, pT-ODNs alone induced only low level expression of two cytokines, CCL2 and CXCL10. The combination of pT-ODNs along with TLR7/8 agonists induced a synergistic response with substantially higher levels of proinflammatory cytokines and chemokines compared to CL075. This enhancement was not due to cellular uptake of the agonist, indicating that the pT-ODN enhancement of cytokine responses was due to effects on an intracellular process. Interestingly, this response was also not due to synergistic stimulation of both TLR7 and TLR8, as the loss of TLR7 abolished the activation of glial cells and cytokine production. Thus, pT-ODNs act in synergy with TLR7/8 agonists to induce strong TLR7-dependent cytokine production in glial cells, suggesting that the combination of pT-ODNs with TLR7 agonists may be a useful mechanism to induce pronounced glial activation in the CNS
Cross-Talk between Signaling Pathways Can Generate Robust Oscillations in Calcium and cAMP
BACKGROUND:To control and manipulate cellular signaling, we need to understand cellular strategies for information transfer, integration, and decision-making. A key feature of signal transduction is the generation of only a few intracellular messengers by many extracellular stimuli. METHODOLOGY/PRINCIPAL FINDINGS:Here we model molecular cross-talk between two classic second messengers, cyclic AMP (cAMP) and calcium, and show that the dynamical complexity of the response of both messengers increases substantially through their interaction. In our model of a non-excitable cell, both cAMP and calcium concentrations can oscillate. If mutually inhibitory, cross-talk between the two second messengers can increase the range of agonist concentrations for which oscillations occur. If mutually activating, cross-talk decreases the oscillation range, but can generate 'bursting' oscillations of calcium and may enable better filtering of noise. CONCLUSION:We postulate that this increased dynamical complexity allows the cell to encode more information, particularly if both second messengers encode signals. In their native environments, it is unlikely that cells are exposed to one stimulus at a time, and cross-talk may help generate sufficiently complex responses to allow the cell to discriminate between different combinations and concentrations of extracellular agonists
- β¦