52 research outputs found
Carrier mode selective working point and side band imbalance in LIGO I
In gravitational wave interferometers, the input laser beam is phase modulated to generate radio-frequency side bands that are used to lock the cavities. The mechanism is the following: the frequency of the side bands and the carrier is chosen in such a way that their response to small changes of the longitudinal degrees of freedom is different. This difference is therefore monitored and it serves as an error signal for controlling the optical cavity lengths, as they are linearly related to the set of observed phases between carrier and side bands. Among the others, one longitudinal degree of freedom is optimally sensitive to the space-time distortions propagating through the cosmos, as predicted by the general theory of relativity. The observation of the astrophysical signal relies on the measurement of that specific degree of freedom. The entire problem is more complex when the transverse degrees of freedom are taken into account, because the relative phase between the fields also depends on their overlap. In order to establish an unambiguous relation between length changes and phase measurements, there must be one circulating optical mode and the only difference between carrier and side bands must be their amplitude. We will show that the variability of the transverse degrees of freedom and their different actions on carrier and side band fields puts a severe limit on this assumption. Unless the system is made of perfect and perfectly matched optical cavities, it is never governed by one unique coherent state and any adjustment of the optical lengths results from a compromise between the lengths that are optimal for the carrier field and the side band ones. Such a compromise alters the correspondence between error signals and cavity lengths, calculated in the one-dimensional treatment. We assess the strength of this effect and relate it to the sensitivity of the instrument (which relies on the reconstruction of that correspondence) in realistic circumstances
Extraction of energy from gravitational waves by laser interferometer detectors
In this paper we discuss the energy interaction between gravitational waves
and laser interferom- eter gravitational wave detectors. We show that the
widely held view that the laser interferometer gravitational wave detector
absorbs no energy from gravitational waves is only valid under the
approximation of a frequency-independent optomechanical coupling strength and a
pump laser without detuning with respect to the resonance of the
interferometer. For a strongly detuned interferometer, the optical-damping
dynamics dissipates gravitational wave energy through the interaction between
the test masses and the optical field. For a non-detuned interferometer, the
frequency-dependence of the optomechanical coupling strength causes a tiny
energy dissipation, which is proved to be equivalent to the Doppler friction
raised by Braginsky et.al.Comment: 20 pages, 7 figure
In situ measurement of absorption in high-power interferometers by using beam diameter measurements
We present a simple technique to make in situ measurements of the absorption in the optics of high-power laser interferometers. The measurement is particularly useful to those commissioning large-scale high power optical systems
Measurement of Birefringence of Low-Loss, High-Reflectance Coating of M-Axis Sapphire
The birefringence of a low-loss, high-reflectance coating applied to an 8-cm-diameter sapphire crystal grown in the m-axis direction has been mapped. By monitoring the transmission of a high-finesse Fabry-Perot cavity as a function of the polarization of the input light, we find an upper limit for the magnitude of the birefringence of 2.5 x 10^-4 rad and an upper limit in the variation in direction of the birefringence of 10 deg. These values are sufficiently small to allow consideration of m-axis sapphire as a substrate material for the optics of the advanced detector at the Laser Interferometer Gravitational Wave Observatory
Evaluation of an AAV2-Based Rapamycin-Regulated Glial Cell Line-Derived Neurotrophic Factor (GDNF) Expression Vector System
Effective regulation of transgene product in anatomically circumscribed brain tissue is dependent on the pharmacokinetics of the regulating agent, the kinetics of transcriptional activation and degradation of the transgene product. We evaluated rapamycin-regulated AAV2-GDNF expression in the rat brain (striatum). Regulated (a dual-component system: AAV2-FBZhGDNF + AAV2-TF1Nc) and constitutive (CMV-driven) expression vectors were compared. Constitutively active AAV2-GDNF directed stable GDNF expression in a dose-dependent manner and it increased for the first month, thereafter reaching a plateau that was maintained over a further 3 months. For the AAV2-regGDNF, rapamycin was administered in a 3-days on/4-days off cycle. Intraperitoneal, oral, and direct brain delivery (CED) of rapamycin were evaluated. Two cycles of rapamycin at an intraperitoneal dose of 10 mg/kg gave the highest GDNF level (2.75±0.01ng/mg protein). Six cycles at 3 mg/kg resulted in lower GDNF values (1.36±0.3 ng/mg protein). Interestingly, CED of rapamycin into the brain at a very low dose (50 ng) induced GDNF levels comparable to a 6-week intraperitoneal rapamycin cycle. This study demonstrates the effectiveness of rapamycin regulation in the CNS. However, the kinetics of the transgene in brain tissue, the regulator dosing amount and schedule are critical parameters that influence the kinetics of accumulation and zenith of the encoded transgene product
A search for weak distortion of distant galaxy images by large-scale structure
We have completed a feasibility study for the measurement of weak distortion of distant galaxy images by intervening large-scale structure by using the 5-m Hale reflector to acquire a very deep, r ~ 26, exposure of a single field. The error budget of our observations is dominated by the effects of atmospheric seeing (which strongly degrades this signal because the faintest images are under-resolved) and telescope effects. After performing a correction for telescope aberrations and possible guiding errors, the observed mean ‘polarization’ of the images of 4363 galaxies with magnitudes 23 ≤ r ≤ 26 within a circle of radius 4.8 arcmin was found to be p̄ =0.01 ± 0.01. The associated two-point polarization correlation function has a constant value of C_(pp) = (1.4 ± 3.0) x 10^(−5) over the angular range 1 to 6 arcmin. It is predicted that the cosmological polarization should be in the range p = 0.03 ± 0.01 for a standard CDM universe normalized by a bias parameter, b, of unity (p scales inversely with b and approximately linearly with Ω_0). For the atmospheric seeing and sky noise conditions associated with our data, Monte Carlo simulations suggest that the efficiency of measuring the mean cosmological polarization is on the order of 40 ± 10 per cent. Thus our preliminary analysis suggests an upper limit on the cosmological mean polarization in the field of p̄_(max) ∼ 0.04. Deep wide-field imaging in 0.5 arcsec seeing to study this polarization signal should provide limits that constrain current cosmological models
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Food for pollinators: quantifying the nectar and pollen resources of urban flower meadows
Planted meadows are increasingly used to improve the biodiversity and aesthetic amenity value of urban areas. Although many ‘pollinator-friendly’ seed mixes are available, the floral resources these provide to flower-visiting insects, and how these change through time, are largely unknown. Such data are necessary to compare the resources provided by alternative meadow seed mixes to each other and to other flowering habitats. We used quantitative surveys of over 2 million flowers to estimate the nectar and pollen resources offered by two exemplar commercial seed mixes (one annual, one perennial) and associated weeds grown as 300m2 meadows across four UK cities, sampled at six time points between May and September 2013. Nectar sugar and pollen rewards per flower varied widely across 65 species surveyed, with native British weed species (including dandelion, Taraxacum agg.) contributing the top five nectar producers and two of the top ten pollen producers. Seed mix species yielding the highest rewards per flower included Leontodon hispidus, Centaurea cyanus and C. nigra for nectar, and Papaver rhoeas, Eschscholzia californica and Malva moschata for pollen. Perennial meadows produced up to 20x more nectar and up to 6x more pollen than annual meadows, which in turn produced far more than amenity grassland controls. Perennial meadows produced resources earlier in the year than annual meadows, but both seed mixes delivered very low resource levels early in the year and these were provided almost entirely by native weeds. Pollen volume per flower is well predicted statistically by floral morphology, and nectar sugar mass and pollen volume per unit area are correlated with flower counts, raising the possibility that resource levels can be estimated for species or habitats where they cannot be measured directly. Our approach does not incorporate resource quality information (for example, pollen protein or essential amino acid content), but can easily do so when suitable data exist. Our approach should inform the design of new seed mixes to ensure continuity in floral resource availability throughout the year, and to identify suitable species to fill resource gaps in established mixes
A framework for human microbiome research
A variety of microbial communities and their genes (the microbiome) exist throughout the human body, with fundamental roles in human health and disease. The National Institutes of Health (NIH)-funded Human Microbiome Project Consortium has established a population-scale framework to develop metagenomic protocols, resulting in a broad range of quality-controlled resources and data including standardized methods for creating, processing and interpreting distinct types of high-throughput metagenomic data available to the scientific community. Here we present resources from a population of 242 healthy adults sampled at 15 or 18 body sites up to three times, which have generated 5,177 microbial taxonomic profiles from 16S ribosomal RNA genes and over 3.5 terabases of metagenomic sequence so far. In parallel, approximately 800 reference strains isolated from the human body have been sequenced. Collectively, these data represent the largest resource describing the abundance and variety of the human microbiome, while providing a framework for current and future studies
Structure, function and diversity of the healthy human microbiome
Author Posting. © The Authors, 2012. This article is posted here by permission of Nature Publishing Group. The definitive version was published in Nature 486 (2012): 207-214, doi:10.1038/nature11234.Studies of the human microbiome have revealed that even healthy individuals differ remarkably in the microbes that occupy habitats such as the gut, skin and vagina. Much of this diversity remains unexplained, although diet, environment, host genetics and early microbial exposure have all been implicated. Accordingly, to characterize the ecology of human-associated microbial communities, the Human Microbiome Project has analysed the largest cohort and set of distinct, clinically relevant body habitats so far. We found the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals. The project encountered an estimated 81–99% of the genera, enzyme families and community configurations occupied by the healthy Western microbiome. Metagenomic carriage of metabolic pathways was stable among individuals despite variation in community structure, and ethnic/racial background proved to be one of the strongest associations of both pathways and microbes with clinical metadata. These results thus delineate the range of structural and functional configurations normal in the microbial communities of a healthy population, enabling future characterization of the epidemiology, ecology and translational applications of the human microbiome.This research was supported in
part by National Institutes of Health grants U54HG004969 to B.W.B.; U54HG003273
to R.A.G.; U54HG004973 to R.A.G., S.K.H. and J.F.P.; U54HG003067 to E.S.Lander;
U54AI084844 to K.E.N.; N01AI30071 to R.L.Strausberg; U54HG004968 to G.M.W.;
U01HG004866 to O.R.W.; U54HG003079 to R.K.W.; R01HG005969 to C.H.;
R01HG004872 to R.K.; R01HG004885 to M.P.; R01HG005975 to P.D.S.;
R01HG004908 to Y.Y.; R01HG004900 to M.K.Cho and P. Sankar; R01HG005171 to
D.E.H.; R01HG004853 to A.L.M.; R01HG004856 to R.R.; R01HG004877 to R.R.S. and
R.F.; R01HG005172 to P. Spicer.; R01HG004857 to M.P.; R01HG004906 to T.M.S.;
R21HG005811 to E.A.V.; M.J.B. was supported by UH2AR057506; G.A.B. was
supported by UH2AI083263 and UH3AI083263 (G.A.B., C. N. Cornelissen, L. K. Eaves
and J. F. Strauss); S.M.H. was supported by UH3DK083993 (V. B. Young, E. B. Chang,
F. Meyer, T. M. S., M. L. Sogin, J. M. Tiedje); K.P.R. was supported by UH2DK083990 (J.
V.); J.A.S. and H.H.K. were supported by UH2AR057504 and UH3AR057504 (J.A.S.);
DP2OD001500 to K.M.A.; N01HG62088 to the Coriell Institute for Medical Research;
U01DE016937 to F.E.D.; S.K.H. was supported by RC1DE0202098 and
R01DE021574 (S.K.H. and H. Li); J.I. was supported by R21CA139193 (J.I. and
D. S. Michaud); K.P.L. was supported by P30DE020751 (D. J. Smith); Army Research
Office grant W911NF-11-1-0473 to C.H.; National Science Foundation grants NSF
DBI-1053486 to C.H. and NSF IIS-0812111 to M.P.; The Office of Science of the US
Department of Energy under Contract No. DE-AC02-05CH11231 for P.S. C.; LANL
Laboratory-Directed Research and Development grant 20100034DR and the US
Defense Threat Reduction Agency grants B104153I and B084531I to P.S.C.; Research
Foundation - Flanders (FWO) grant to K.F. and J.Raes; R.K. is an HHMI Early Career
Scientist; Gordon&BettyMoore Foundation funding and institutional funding fromthe
J. David Gladstone Institutes to K.S.P.; A.M.S. was supported by fellowships provided by
the Rackham Graduate School and the NIH Molecular Mechanisms in Microbial
Pathogenesis Training Grant T32AI007528; a Crohn’s and Colitis Foundation of
Canada Grant in Aid of Research to E.A.V.; 2010 IBM Faculty Award to K.C.W.; analysis
of the HMPdata was performed using National Energy Research Scientific Computing
resources, the BluBioU Computational Resource at Rice University
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