1,373 research outputs found
The Cluster-EAGLE project: Velocity bias and the velocity dispersion-mass relation of cluster galaxies
We use the Cluster-EAGLE simulations to explore the velocity bias introduced when using galaxies, rather than dark matter particles, to estimate the velocity dispersion of a galaxy cluster, a property known to be tightly correlated with cluster mass. The simulations consist of 30 clusters spanning a mass range 14.0 ≤ log 10 (M 200 c /M ⊙ ) ≤ 15.4, with their sophisticated subgrid physics modelling and high numerical resolution (subkpc gravitational softening), making them ideal for this purpose. We find that selecting galaxies by their total mass results in a velocity dispersion that is 5-10 per cent higher than the dark matter particles. However, selecting galaxies by their stellar mass results in an almost unbiased ( < 5 per cent) estimator of the velocity dispersion. This result holds out to z = 1.5 and is relatively insensitive to the choice of cluster aperture, varying by less than 5 per cent between r 500 c and r 200m . We show that the velocity bias is a function of the time spent by a galaxy inside the cluster environment. Selecting galaxies by their total mass results in a larger bias because a larger fraction of objects have only recently entered the cluster and these have a velocity bias above unity. Galaxies that entered more than 4 Gyr ago become progressively colder with time, as expected from dynamical friction. We conclude that velocity bias should not be a major issue when estimating cluster masses from kinematic methods
Terms and nomenclature used for plant-derived components in nutrition and related research: efforts toward harmonization.
Determining the Contribution of Epidermal Cell Shape to Petal Wettability Using Isogenic Antirrhinum Lines
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Quantum control of hybrid nuclear-electronic qubits
Pulsed magnetic resonance is a wide-reaching technology allowing the quantum
state of electronic and nuclear spins to be controlled on the timescale of
nanoseconds and microseconds respectively. The time required to flip either
dilute electronic or nuclear spins is orders of magnitude shorter than their
decoherence times, leading to several schemes for quantum information
processing with spin qubits. We investigate instead the novel regime where the
eigenstates approximate 50:50 superpositions of the electronic and nuclear spin
states forming "hybrid nuclear-electronic" qubits. Here we demonstrate quantum
control of these states for the first time, using bismuth-doped silicon, in
just 32 ns: this is orders of magnitude faster than previous experiments where
pure nuclear states were used. The coherence times of our states are five
orders of magnitude longer, reaching 4 ms, and are limited by the
naturally-occurring 29Si nuclear spin impurities. There is quantitative
agreement between our experiments and no-free-parameter analytical theory for
the resonance positions, as well as their relative intensities and relative
Rabi oscillation frequencies. In experiments where the slow manipulation of
some of the qubits is the rate limiting step, quantum computations would
benefit from faster operation in the hybrid regime.Comment: 20 pages, 8 figures, new data and simulation
Effect of protocatechuic acid on insulin responsiveness and inflammation in visceral adipose tissue from obese individuals: possible role for PTP1B
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Impact of Space Weather on Climate and Habitability of Terrestrial Type Exoplanets
The current progress in the detection of terrestrial type exoplanets has
opened a new avenue in the characterization of exoplanetary atmospheres and in
the search for biosignatures of life with the upcoming ground-based and space
missions. To specify the conditions favorable for the origin, development and
sustainment of life as we know it in other worlds, we need to understand the
nature of astrospheric, atmospheric and surface environments of exoplanets in
habitable zones around G-K-M dwarfs including our young Sun. Global environment
is formed by propagated disturbances from the planet-hosting stars in the form
of stellar flares, coronal mass ejections, energetic particles, and winds
collectively known as astrospheric space weather. Its characterization will
help in understanding how an exoplanetary ecosystem interacts with its host
star, as well as in the specification of the physical, chemical and biochemical
conditions that can create favorable and/or detrimental conditions for
planetary climate and habitability along with evolution of planetary internal
dynamics over geological timescales. A key linkage of (astro) physical,
chemical, and geological processes can only be understood in the framework of
interdisciplinary studies with the incorporation of progress in heliophysics,
astrophysics, planetary and Earth sciences. The assessment of the impacts of
host stars on the climate and habitability of terrestrial (exo)planets will
significantly expand the current definition of the habitable zone to the
biogenic zone and provide new observational strategies for searching for
signatures of life. The major goal of this paper is to describe and discuss the
current status and recent progress in this interdisciplinary field and to
provide a new roadmap for the future development of the emerging field of
exoplanetary science and astrobiology.Comment: 206 pages, 24 figures, 1 table; Review paper. International Journal
of Astrobiology (2019
Cytotoxic lymphocytes in B-cell chronic lymphocytic leukemia
The occurrence of cytotoxic lymphocyte subpopulations (i.e., CD 16+, CD57+ and cytotoxic CD 8+) was studied in the peripheral blood of 18 B-cell chronic lymphocytic leukemia (B-CLL) patients. The absolute numbers of CD 57+, CD 16+ and cytotoxic CD 8+ lymphocytes were increased in the peripheral blood of untreated patients as compared with healthy donors, suggesting a causal relation with the accumulation of malignant B-cells. For 5 B-CLL patients and 5 hematological normal donors, the lymphocyte subpopulations in peripheral blood, lymph nodes and bone marrow were determined. A significant immune response was observed in the lymph nodes of the patients, as reflected by the CD 3+ lymphocytes, which were 1.7–27 times larger in the patients lymph nodes than in their peripheral blood and bone marrow. In contrast, with peripheral blood this was mainly caused by an increase in CD 4+ lymphocytes. The CD 57 lymphocytes in the lymph nodes of the patients had abnormal orthogonal light-scattering signals and an abnormal density of CD 57+ receptors in comparison with their peripheral blood CD 57+ lymphocytes or the CD57+ lymphocytes in the peripheral blood, bone marrow and tonsils of the hematological normal donors. This study shows that although a significant increase of cytotoxic lymphocytes in the peripheral blood of B-CLL patients is observed, the actual distributions of the non-malignant lymphocytes can be quite different at the actual tumor sites, i.e., bone marrow and lymph node
Anti-Allergic Cromones Inhibit Histamine and Eicosanoid Release from Activated Human and Murine Mast Cells by Releasing Annexin A1
PMCID: PMC3601088This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients
Background
Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic deletion of approximately 27 genes on chromosome 7, at locus 7q11.23. WS is characterised by an uneven cognitive profile, with serious deficits in visuospatial tasks in comparison to relatively proficient performance in some other cognitive domains such as language and face processing. Individuals with partial genetic deletions within the WS critical region (WSCR) have provided insights into the contribution of specific genes to this complex phenotype. However, the combinatorial effects of different genes remain elusive.
Methods
We report on visuospatial cognition in two individuals with contrasting partial deletions in the WSCR: one female (HR), aged 11 years 9 months, with haploinsufficiency for 24 of the WS genes (up to GTF2IRD1), and one male (JB), aged 14 years 2 months, with the three most telomeric genes within the WSCR deleted, or partially deleted.
Results
Our in-depth phenotyping of the visuospatial domain from table-top psychometric, and small- and large-scale experimental tasks reveal a profile in HR in line with typically developing controls, albeit with some atypical features. These data are contrasted with patient JB’s atypical profile of strengths and weaknesses across the visuospatial domain, as well as with more substantial visuospatial deficits in individuals with the full WS deletion.
Conclusions
Our findings point to the contribution of specific genes to spatial processing difficulties associated with WS, highlighting the multifaceted nature of spatial cognition and the divergent effects of genetic deletions within the WSCR on different components of visuospatial ability. The importance of general transcription factors at the telomeric end of the WSCR, and their combinatorial effects on the WS visuospatial phenotype are also discussed
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