•Pluto and Charon are rock rich while the small satellites are mostly water ice.•Charon is about 10% icier than Pluto.•A giant impact origin involving partially differentiated precursors ...supported.•Formation of entire PC system in a collapsing, rotating pebble cloud not supported.•Slow, late accretion of impact precursors indicated.
New Horizon's accurate determination of the sizes and densities of Pluto and Charon now permit precise internal models of both bodies to be constructed. Assuming differentiated rock-ice structures, we find that Pluto is close to 2/3 solar-composition anhydrous rock by mass and Charon 3/5 solar-composition anhydrous rock by mass. Pluto and Charon are closer to each other in density than to other large (≳1000-km diameter) Kuiper belt bodies. Despite this, we show that neither the possible presence of an ocean under Pluto's water ice shell (and no ocean within Charon), nor enhanced porosity at depth in Charon's icy crust compared with that of Pluto, are sufficient to make Pluto and Charon's rock mass fractions match. All four small satellites (Styx, Nix, Kerberos, Hydra) appear much icier in comparison with either Pluto or Charon. In terms of a giant impact origin, both these inferences are most consistent with the relatively slow collision of partly differentiated precursor bodies (Canup, Astrophys. J. 141, 35, 2011). This is in turn consistent with dynamical conditions in the ancestral Kuiper belt, but implies that the impact precursors themselves accreted relatively late and slowly (to limit 26Al and accretional heating). The iciness of the small satellites is not consistent with direct formation of the Pluto–Charon system from a streaming instability in the solar nebula followed by prompt collapse of gravitationally bound “pebble piles,” a proposed formation mechanism for Kuiper belt binaries (Nesvorný et al., Astron. J. 140, 785–793, 2010). Growth of Pluto-scale bodies by accretion of pebbles in the ancestral Kuiper belt is not ruled out, however, and may be needed to prevent the precursor bodies from fully differentiating, due to buried accretional heat, prior to the Charon-forming impact.
This selection from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Head and Neck Cancers focuses on glottic laryngeal cancer, which is the most common type of laryngeal ...cancer and has an excellent cure rate. The lymphatic drainage of the glottis is sparse, and early stage primaries rarely spread to regional nodes. Because hoarseness is an early symptom, most glottic laryngeal cancer is early stage at diagnosis. Updates to these guidelines for 2014 include revisions to "Principles of Radiation Therapy" for each site and "Principles of Surgery," and the addition of a new section on "Principles of Dental Evaluation and Management."
While acetylated, RNA-binding-deficient TDP-43 reversibly phase separates within nuclei into complex droplets (anisosomes) comprised of TDP-43-containing liquid outer shells and liquid centres of ...HSP70-family chaperones, cytoplasmic aggregates of TDP-43 are hallmarks of multiple neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Here we show that transient oxidative stress, proteasome inhibition or inhibition of the ATP-dependent chaperone activity of HSP70 provokes reversible cytoplasmic TDP-43 de-mixing and transition from liquid to gel/solid, independently of RNA binding or stress granules. Isotope labelling mass spectrometry was used to identify that phase-separated cytoplasmic TDP-43 is bound by the small heat-shock protein HSPB1. Binding is direct, mediated through TDP-43's RNA binding and low-complexity domains. HSPB1 partitions into TDP-43 droplets, inhibits TDP-43 assembly into fibrils, and is essential for disassembly of stress-induced TDP-43 droplets. A decrease in HSPB1 promotes cytoplasmic TDP-43 de-mixing and mislocalization. HSPB1 depletion was identified in spinal motor neurons of patients with ALS containing aggregated TDP-43. These findings identify HSPB1 to be a regulator of cytoplasmic TDP-43 phase separation and aggregation.
During the coronavirus disease-2019 (COVID-19) pandemic, severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) has led to the infection of millions of people and has claimed hundreds ...of thousands of lives. The entry of the virus into cells depends on the receptor-binding domain (RBD) of the spike (S) protein of SARS-CoV-2. Although there is currently no vaccine, it is likely that antibodies will be essential for protection. However, little is known about the human antibody response to SARS-CoV-2
. Here we report on 149 COVID-19-convalescent individuals. Plasma samples collected an average of 39 days after the onset of symptoms had variable half-maximal pseudovirus neutralizing titres; titres were less than 50 in 33% of samples, below 1,000 in 79% of samples and only 1% of samples had titres above 5,000. Antibody sequencing revealed the expansion of clones of RBD-specific memory B cells that expressed closely related antibodies in different individuals. Despite low plasma titres, antibodies to three distinct epitopes on the RBD neutralized the virus with half-maximal inhibitory concentrations (IC
values) as low as 2 ng ml
. In conclusion, most convalescent plasma samples obtained from individuals who recover from COVID-19 do not contain high levels of neutralizing activity. Nevertheless, rare but recurring RBD-specific antibodies with potent antiviral activity were found in all individuals tested, suggesting that a vaccine designed to elicit such antibodies could be broadly effective.
Io After Galileo Lopes, Rosaly M.C; Spencer, John
2007, 2006
eBook
Written by experts in the field, many of whom took part in the Galileo mission, the book reviews the basics about Io and its unique space environment. Coverage includes all subjects, where the ...Galilio mission has shed new light on, with some emphasis on Io's most remarkable characteristics: its active volcanism. Written primarily for planetary scientiests this book will also benefit volcanologists in general and newcomers wishing to specialize in this field of research.
In the summer and autumn of 2015, the Bellinger River snapping turtle (Myuchelys georgesi), a narrow‐range endemic of eastern New South Wales, Australia, suffered mass mortality from epidemic ...disease, apparently caused by a previously unknown virus. Information on the current population size and structure of M. georgesi, and the body condition and growth of the surviving individuals, is needed to support planning of conservation actions. Population estimates are also needed for a sympatric population of the widely distributed Macquarie turtle (Emydura macquarii), which has probably been introduced to the Bellinger River and may threaten the persistence of M. georgesi through hybridization, competition, and disease transmission.
Data from five turtle surveys between November 2015 and November 2018 were used to estimate populations of the two species in the Bellinger River by an analysis based on habitat extent and turtle detectability. Changes in the body condition of M. georgesi and the body growth of both species were also assessed.
Current populations of ~150 M. georgesi and ~500 E. macquarii are indicated, although the uncertainty of these estimates is high. The estimate for M. georgesi represents a decline of >90% from the historical population. Moreover, about 88% of the surviving M. georgesi are immature, and only about 5% are mature females. However, the body condition of the survivors has improved recently. Growth models suggest that M. georgesi matures later than E. macquarii, which may provide the latter with a competitive advantage.
Evidence presented here does not support a previous hypothesis that M. georgesi were predisposed to disease through malnutrition and consequently reduced immune competence caused by high water temperatures and low river flows. Continuing disease, hybridization, and interspecific competition are probably the greatest threats to the persistence of the species.
Tremendous scientific progress has been achieved through the development of nonlinear integrated photonics. Prominent examples are Kerr frequency comb generation in microresonators, and ...supercontinuum generation and frequency conversion in nonlinear photonic waveguides. A high conversion efficiency is enabling for applications of nonlinear optics, including such broad directions as high‐speed optical signal processing, metrology, and quantum communication and computation. In this work, a gallium‐arsenide‐on‐insulator (GaAs) platform for nonlinear photonics is demonstrated. GaAs has among the highest second‐ and third‐order nonlinear optical coefficients, and the use of a silica cladding results in waveguides with a large refractive index contrast and low propagation loss for expanded designs of nonlinear processes. By harnessing these properties and developing nanofabrication with GaAs, a record normalized second‐harmonic efficiency of 13 000% W−1 cm−2 at a fundamental wavelength of 2 µm is reported. This work paves the way for high performance nonlinear photonic integrated circuits, which not only can transition advanced functionalities outside the lab through fundamentally reduced power consumption and footprint, but also enables future optical sources and detectors.
A gallium‐arsenide‐on‐insulator platform for integrated nonlinear photonics is demonstrated on silicon substrate. Waveguides on this platform have high nonlinear coefficients, large index contrasts, and low propagation losses. By harnessing those properties, a second‐harmonic generation with a record‐normalized efficiency of 13 000% W−1 cm−2 is achieved. This work paves the way to high performance nonlinear photonic integrated circuits.
The epigenome represents a vast molecular apparatus that writes, reads, and erases chemical modifications to the DNA and histone code without changing the DNA base-pair sequence itself. Recent ...advances in molecular sequencing technology have revealed that epigenetic chromatin marks directly mediate critical events in retinal development, aging, and degeneration. Epigenetic signaling regulates retinal progenitor (RPC) cell cycle exit during retinal laminar development, giving rise to retinal ganglion cells (RGCs), amacrine cells, horizontal cells, bipolar cells, photoreceptors, and Müller glia. Age-related epigenetic changes such as DNA methylation in the retina and optic nerve are accelerated in pathogenic conditions such as glaucoma and macular degeneration, but reversing these epigenetic marks may represent a novel therapeutic target. Epigenetic writers also integrate environmental signals such as hypoxia, inflammation, and hyperglycemia in complex retinal conditions such as diabetic retinopathy (DR) and choroidal neovascularization (CNV). Histone deacetylase (HDAC) inhibitors protect against apoptosis and photoreceptor degeneration in animal models of retinitis pigmentosa (RP). The epigenome represents an intriguing therapeutic target for age-, genetic-, and neovascular-related retinal diseases, though more work is needed before advancement to clinical trials.
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