296 research outputs found
Bulk Composition of GJ 1214b and other sub-Neptune exoplanets
GJ1214b stands out among the detected low-mass exoplanets, because it is, so
far, the only one amenable to transmission spectroscopy. Up to date there is no
consensus about the composition of its envelope although most studies suggest a
high molecular weight atmosphere. In particular, it is unclear if hydrogen and
helium are present or if the atmosphere is water dominated. Here, we present
results on the composition of the envelope obtained by using an internal
structure and evolutionary model to fit the mass and radius data. By examining
all possible mixtures of water and H/He, with the corresponding opacities, we
find that the bulk amount of H/He of GJ1214b is at most 7% by mass. In general,
we find the radius of warm sub-Neptunes to be most sensitive to the amount of
H/He. We note that all (Kepler-11b,c,d,f, Kepler-18b, Kepler-20b, 55Cnc-e,
Kepler-36c and Kepler-68b) but two (Kepler-11e and Kepler-30b) of the
discovered low-mass planets so far have less than 10% H/He. In fact, Kepler-11e
and Kepler-30b have 10-18% and 5-15% bulk H/He. Conversely, little can be
determined about the H2O or rocky content of sub-Neptune planets. We find that
although a 100% water composition fits the data for GJ1214b, based on formation
constraints the presence of heavier refractory material on this planet is
expected, and hence, so is a component lighter than water required. A robust
determination by transmission spectroscopy of the composition of the upper
atmosphere of GJ1214b will help determine the extent of compositional
segregation between the atmosphere and envelope.Comment: Updated the masses and radii of the Kepler-11 system, added
Kepler-30b as well in the analysis. Accepted in ApJ, 39 pages, 9 figure
Development and validation of a real-time two-step RT-qPCR TaqMan (R) assay for quantitation of Sacbrood virus (SBV) and its application to a field survey of symptomatic honey bee colonies
Sacbrood virus (SBV) is the causal agent of a disease of honey bee larvae, resulting in failure to pupate and causing death. The typical clinical symptom of SBV is an accumulation of SBV-rich fluid in swollen subcuticular pouches, forming the characteristic fluid-filled sac that gives its name to the disease. Outbreaks of the disease have been reported in different countries, affecting the development of the brood and causing losses in honey bee colonies. Today, few data are available on the SBV viral load in the case of overt disease in larvae, or for the behavioural changes of SBV-infected adult bees. A two-step real-time RT-PCR assay, based on TaqMan (R) technology using a fluorescent probe (FAM-TAMRA) was therefore developed to quantify Sacbrood virus in larvae, pupae and adult bees from symptomatic apiaries. This assay was first validated according to the recent XP-U47-600 standard issued by the French Standards Institute, where the reliability and the repeatability of the results and the performance of the assay were confirmed. The performance of the qPCR assay was validated over the 6 log range of the standard curve (i.e. from 10(2) to 10(8) copies per well) with a measurement uncertainty evaluated at 0.11 log(10). The detection and quantitation limits were established respectively at 50 copies and 100 copies of SBV genome, for a template volume of 5 mu l of cDNA. The RT-qPCR assay was applied during a French SBV outbreak in 2012 where larvae with typical SBV signs were collected, along with individuals without clinical signs. The SBV quantitation revealed that, in symptomatic larvae, the virus load was significantly higher than in samples without clinical signs. Combining quantitation with clinical data, a threshold of SBV viral load related to an overt disease was proposed (10(10) SBV genome copies per individual)
Atmospheric circulation of hot Jupiters: Coupled radiative-dynamical general circulation model simulations of HD 189733b and HD 209458b
We present global, three-dimensional numerical simulations of HD 189733b and
HD 209458b that couple the atmospheric dynamics to a realistic representation
of non-gray cloud-free radiative transfer. The model, which we call the
Substellar and Planetary Atmospheric Radiation and Circulation (SPARC) model,
adopts the MITgcm for the dynamics and uses the radiative model of McKay,
Marley, Fortney, and collaborators for the radiation. Like earlier work with
simplified forcing, our simulations develop a broad eastward equatorial jet,
mean westward flow at higher latitudes, and substantial flow over the poles at
low pressure. For HD 189733b, our simulations without TiO and VO opacity can
explain the broad features of the observed 8 and 24-micron light curves,
including the modest day-night flux variation and the fact that the planet/star
flux ratio peaks before the secondary eclipse. Our simulations also provide
reasonable matches to the Spitzer secondary-eclipse depths at 4.5, 5.8, 8, 16,
and 24 microns and the groundbased upper limit at 2.2 microns. However, we
substantially underpredict the 3.6-micron secondary-eclipse depth, suggesting
that our simulations are too cold in the 0.1-1 bar region. Predicted temporal
variability in secondary-eclipse depths is ~1% at Spitzer bandpasses,
consistent with recent observational upper limits at 8 microns. We also show
that nonsynchronous rotation can significantly alter the jet structure. For HD
209458b, we include TiO and VO opacity; these simulations develop a hot (>2000
K) dayside stratosphere. Despite this stratosphere, we do not reproduce current
Spitzer photometry of this planet. Light curves in Spitzer bandpasses show
modest phase variation and satisfy the observational upper limit on day-night
phase variation at 8 microns. (abridged)Comment: 20 pages (emulate-apj format), 21 figures, final version now
published in ApJ. Includes expanded discussion of radiative-transfer methods
and two new figure
The Roles of Tidal Evolution and Evaporative Mass Loss in the Origin of CoRoT-7 b
CoRoT-7 b is the first confirmed rocky exoplanet, but, with an orbital
semi-major axis of 0.0172 AU, its origins may be unlike any rocky planet in our
solar system. In this study, we consider the roles of tidal evolution and
evaporative mass loss in CoRoT-7 b's history, which together have modified the
planet's mass and orbit. If CoRoT-7 b has always been a rocky body, evaporation
may have driven off almost half its original mass, but the mass loss may depend
sensitively on the extent of tidal decay of its orbit. As tides caused CoRoT-7
b's orbit to decay, they brought the planet closer to its host star, thereby
enhancing the mass loss rate. Such a large mass loss also suggests the
possibility that CoRoT-7 b began as a gas giant planet and had its original
atmosphere completely evaporated. In this case, we find that CoRoT-7 b's
original mass probably didn't exceed 200 Earth masses (about 2/3 of a Jupiter
mass). Tides raised on the host star by the planet may have significantly
reduced the orbital semi-major axis, perhaps causing the planet to migrate
through mean-motion resonances with the other planet in the system, CoRoT-7 c.
The coupling between tidal evolution and mass loss may be important not only
for CoRoT-7 b but also for other close-in exoplanets, and future studies of
mass loss and orbital evolution may provide insight into the origin and fate of
close-in planets, both rocky and gaseous.Comment: Accepted for publication by MNRAS on 2010 May
Validity, Reliability, and Differential Item Functioning of English and French Versions of the 10-Item Connor-Davidson Resilience Scale in Systemic Sclerosis: A Scleroderma Patient-Centered Intervention Network Cohort Study
Objective
Some individuals with systemic sclerosis (SSc) report positive mental health, despite severe disease manifestations, which may be associated with resilience, but no resilience measure has been validated in SSc. This study was undertaken to assess the validity, reliability, and differential item functioning (DIF) between English- and French-language versions of the 10-item Connor-Davidson Resilience Scale (CD-RISC-10) in SSc.
Methods
Eligible participants were enrolled in the Scleroderma Patient-centered Intervention Network Cohort and completed the CD-RISC-10 between August 2022 and January 2023. We used confirmatory factor analysis (CFA) to evaluate the CD-RISC-10 factor structure and conducted DIF analysis across languages with Multiple Indicators Multiple Causes models. We tested convergent validity with another measure of resilience and measures of self-esteem and depression and anxiety symptoms. We assessed internal consistency and test–retest reliability using Cronbach\u27s alpha and intraclass correlation coefficient (ICC).
Results
A total of 962 participants were included in this analysis. CFA supported a single-factor structure (Tucker–Lewis index = 0.99, comparative fit index = 0.99, root mean square error of approximation = 0.08 [90% confidence interval (90% CI) 0.07, 0.09]). We found no meaningful DIF. Internal consistency was high (α = 0.93 [95% CI 0.92, 0.94]), and we found that correlations with other measures of psychological functioning were moderate to large (|r| = 0.57–0.78) and confirmed study hypotheses. The scale showed good 1–2-week test–retest reliability (ICC 0.80 [95% CI 0.75, 0.85]) in a subsample of 230 participants.
Conclusion
The CD-RISC-10 is a valid and reliable measure of resilience in SSc, with score comparability across English and French versions
BioHealthBase: informatics support in the elucidation of influenza virus host–pathogen interactions and virulence
The BioHealthBase Bioinformatics Resource Center (BRC) (http://www.biohealthbase.org) is a public bioinformatics database and analysis resource for the study of specific biodefense and public health pathogens—Influenza virus, Francisella tularensis, Mycobacterium tuberculosis, Microsporidia species and ricin toxin. The BioHealthBase serves as an extensive integrated repository of data imported from public databases, data derived from various computational algorithms and information curated from the scientific literature. The goal of the BioHealthBase is to facilitate the development of therapeutics, diagnostics and vaccines by integrating all available data in the context of host–pathogen interactions, thus allowing researchers to understand the root causes of virulence and pathogenicity. Genome and protein annotations can be viewed either as formatted text or graphically through a genome browser. 3D visualization capabilities allow researchers to view proteins with key structural and functional features highlighted. Influenza virus host–pathogen interactions at the molecular/cellular and systemic levels are represented. Host immune response to influenza infection is conveyed through the display of experimentally determined antibody and T-cell epitopes curated from the scientific literature or as derived from computational predictions. At the molecular/cellular level, the BioHealthBase BRC has developed biological pathway representations relevant to influenza virus host–pathogen interaction in collaboration with the Reactome database (http://www.reactome.org)
OPV strains circulation in HIV infected infants after National Immunisation Days in Bangui, Central African Republic
<p>Abstract</p> <p>Background</p> <p>Humans are the only host of polioviruses, thus the prospects of global polio eradication look reasonable. However, individuals with immunodeficiencies were shown to excrete vaccine derived poliovirus for long periods of time which led to reluctance to prolong the vaccination campaign for fear of this end result. Therefore, we aimed to assess the duration of excretion of poliovirus after the 2001 National Immunization Days according to Human immunodeficiency virus status.</p> <p>Findings</p> <p>Fifty three children were enrolled. Sequential stool samples were collected in between National Immunisation Days rounds and then every month during one year. Children were classified into 2 groups: no immunodepression (n = 38), immunodepression (n = 15) according to CD4+ lymphocytes cells count. Thirteen poliovirus strains were isolated from 11 children: 5 Human immunodeficiency virus positive and 6 Human immunodeficiency virus negative. None of the children excreted poliovirus for more than 4 weeks. The restriction fragment length polymorphism analysis showed that all strains were of Sabin origin including a unique Polio Sabine Vaccine types 2 and 3 (S2/S3) recombinant.</p> <p>Conclusions</p> <p>From these findings we assume that Human immunodeficiency virus positive children are not a high risk population for long term poliovirus excretion. More powerful studies are needed to confirm our findings.</p
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