Linking the evolution of terrestrial interiors and an early outgassed atmosphere to astrophysical observations

A terrestrial planet is molten during formation and may remain so if subject to intense insolation or tidal forces. Observations continue to favour the detection and characterisation of hot planets, potentially with large outgassed atmospheres. We aim to determine the radius of hot Earth-like planets with large outgassed atmospheres and explore differences between molten and solid silicate planets and their influence on the mass-radius relationship and transmission and emission spectra. An interior-atmosphere model, combined with static structure calculations, tracks the evolving radius of a rocky mantle that is outgassing CO$_2$ and H$_2$O. Synthetic emission and transmission spectra are generated for CO$_2$ and H$_2$O dominated atmospheres. Atmospheres dominated by CO$_2$ suppress the outgassing of H$_2$O to a greater extent than previously realised, as previous studies have applied an erroneous relationship between volatile mass and partial pressure. We therefore predict more H$_2$O can be retained by the interior during the later stages of magma ocean crystallisation. Furthermore, formation of a lid at the surface can tie outgassing of H$_2$O to the efficiency of heat transport through the lid, rather than the atmosphere's radiative timescale. Contraction of the mantle as it solidifies gives $\sim5\%$ radius decrease, which can partly be offset by addition of a relatively light species to the atmosphere. We conclude that a molten silicate mantle can increase the radius of a terrestrial planet by around $5\%$ compared to its solid counterpart, or equivalently account for a $13\%$ decrease in bulk density. An outgassing atmosphere can perturb the total radius according to its speciation. Atmospheres of terrestrial planets around M-stars that are dominated by CO$_2$ or H$_2$O can be distinguished by observing facilities with extended wavelength coverage (e.g., JWST).Comment: 19 pages, published in A&A, abstract shortene

Improving I/O Performance using Cache as a Service on Cloud

Caching is gaining popularity in Cloud world. It is one of the key technologies which plays a major role in bridging the performance gap between memory hierarchies through spatial or temporal localities. In cloud systems, heavy I/O activities are associated with different applications. Due to heavy I/O activities, performance is degrading. If caching is implemented, these applications would be benefited the most. The use of a Cache as a Service (CaaS) model as a cost efficient cache solution to the disk I/O problem. We have built the remote-memory based cache that is pluggable and file system independent to support various configurations. The cloud Server process introduce, pricing model together with the elastic cache system. This will increase the disk I/O performance of the IaaS, and it will reduce the usage of the physical machines. DOI: 10.17762/ijritcc2321-8169.150516

Genome-wide association study in two cohorts from a multi-generational mouse advanced intercross line highlights the difficulty of replication due to study-specific heterogeneity

There has been extensive discussion of the Replication Crisis in many fields, including genome-wide association studies

Ruptured rudimentary horn of the unicornuate uterus at 16 weeks of pregnancy: a case report

Pregnancy in the rudimentary horn of the uterus is a rare form of ectopic pregnancy; most of the cases were being diagnosed at laparotomy for haemorrhagic shock due to rupture when the patient presents in the second trimester. Pre-rupture diagnosis is possible in the early pregnancy in suspicious cases. Pregnancy in the rudimentary horn has a poor maternal and foetal outcome and 90% of them present with intraperitoneal haemorrhage in the second trimester due to rupture of the horn. We report a case of ruptured rudimentary horn pregnancy at 16weeks, in shock with severe anaemia. Excision of the rudimentary horn with right salpingectomy was done

Induction of Type I Interferon Signaling Determines the Relative Pathogenicity of Staphylococcus aureus Strains

The tremendous success of S. aureus as a human pathogen has been explained primarily by its array of virulence factors that enable the organism to evade host immunity. Perhaps equally important, but less well understood, is the importance of the intensity of the host response in determining the extent of pathology induced by S. aureus infection, particularly in the pathogenesis of pneumonia. We compared the pathogenesis of infection caused by two phylogenetically and epidemiologically distinct strains of S. aureus whose behavior in humans has been well characterized. Induction of the type I IFN cascade by strain 502A, due to a NOD2-IRF5 pathway, was the major factor in causing severe pneumonia and death in a murine model of pneumonia and was associated with autolysis and release of peptidogylcan. In contrast to USA300, 502A was readily eliminated from epithelial surfaces in vitro. Nonetheless, 502A caused significantly increased tissue damage due to the organisms that were able to invade systemically and trigger type I IFN responses, and this was ameliorated in Ifnar-/- mice. The success of USA300 to cause invasive infection appears to depend upon its resistance to eradication from epithelial surfaces, but not production of specific toxins. Our studies illustrate the important and highly variable role of type I IFN signaling within a species and suggest that targeted immunomodulation of specific innate immune signaling cascades may be useful to prevent the excessive morbidity associated with S. aureus pneumonia

Adeno-associated virus type 2 infection activates caspase dependent and independent apoptosis in multiple breast cancer lines but not in normal mammary epithelial cells

<p>Abstract</p> <p>Background</p> <p>In normal cells proliferation and apoptosis are tightly regulated, whereas in tumor cells the balance is shifted in favor of increased proliferation and reduced apoptosis. Anticancer agents mediate tumor cell death via targeting multiple pathways of programmed cell death. We have reported that the non-pathogenic, tumor suppressive Adeno-Associated Virus Type 2 (AAV2) induces apoptosis in Human Papillomavirus (HPV) positive cervical cancer cells, but not in normal keratinocytes. In the current study, we examined the potential of AAV2 to inhibit proliferation of MCF-7 and MDA-MB-468 (both weakly invasive), as well as MDA-MB-231 (highly invasive) human breast cancer derived cell lines. As controls, we used normal human mammary epithelial cells (nHMECs) isolated from tissue biopsies of patients undergoing breast reduction surgery.</p> <p>Results</p> <p>AAV2 infected MCF-7 line underwent caspase-independent, and MDA-MB-468 and MDA-MB-231 cell lines underwent caspase-dependent apoptosis. Death of MDA-MB-468 cells was marked by caspase-9 activation, whereas death of MDA-MB-231 cells was marked by activation of both caspase-8 and caspase-9, and resembled a mixture of apoptotic and necrotic cell death. Cellular demise was correlated with the ability of AAV2 to productively infect and differentially express AAV2 non-structural proteins: Rep78, Rep68 and Rep40, dependent on the cell line. Cell death in the MCF-7 and MDA-MB-231 lines coincided with increased S phase entry, whereas the MDA-MB-468 cells increasingly entered into G2. AAV2 infection led to decreased cell viability which correlated with increased expression of proliferation markers c-Myc and Ki-67. In contrast, nHMECs that were infected with AAV2 failed to establish productive infection or undergo apoptosis.</p> <p>Conclusion</p> <p>AAV2 regulated enrichment of cell cycle check-point functions in G1/S, S and G2 phases could create a favorable environment for Rep protein expression. Inherent Rep associated endonuclease activity and AAV2 genomic hair-pin ends have the potential to induce a cellular DNA damage response, which could act in tandem with c-Myc regulated/sensitized apoptosis induction. In contrast, failure of AAV2 to productively infect nHMECs could be clinically advantageous. Identifying the molecular mechanisms of AAV2 targeted cell cycle regulation of death inducing signals could be harnessed for developing novel therapeutics for weakly invasive as well as aggressive breast cancer types.</p

Using child-friendly movie stimuli to study the development of face, place, and object regions from age 3 to 12 years

Scanning young children while they watch short, engaging, commercially‐produced movies has emerged as a promising approach for increasing data retention and quality. Movie stimuli also evoke a richer variety of cognitive processes than traditional experiments, allowing the study of multiple aspects of brain development simultaneously. However, because these stimuli are uncontrolled, it is unclear how effectively distinct profiles of brain activity can be distinguished from the resulting data. Here we develop an approach for identifying multiple distinct subject‐specific Regions of Interest (ssROIs) using fMRI data collected during movie‐viewing. We focused on the test case of higher‐level visual regions selective for faces, scenes, and objects. Adults (N = 13) were scanned while viewing a 5.6‐min child‐friendly movie, as well as a traditional localizer experiment with blocks of faces, scenes, and objects. We found that just 2.7 min of movie data could identify subject‐specific face, scene, and object regions. While successful, movie‐defined ssROIS still showed weaker domain selectivity than traditional ssROIs. Having validated our approach in adults, we then used the same methods on movie data collected from 3 to 12‐year‐old children (N = 122). Movie response timecourses in 3‐year‐old children's face, scene, and object regions were already significantly and specifically predicted by timecourses from the corresponding regions in adults. We also found evidence of continued developmental change, particularly in the face‐selective posterior superior temporal sulcus. Taken together, our results reveal both early maturity and functional change in face, scene, and object regions, and more broadly highlight the promise of short, child‐friendly movies for developmental cognitive neuroscience

Spermatogenesis drives rapid gene creation and masculinization of the X chromosome in stalk-eyed flies (Diopsidae)

Throughout their evolutionary history, genomes acquire new genetic material that facilitates phenotypic innovation and diversification. Developmental processes associated with reproduction are particularly likely to involve novel genes. Abundant gene creation impacts the evolution of chromosomal gene content and general regulatory mechanisms such as dosage compensation. Numerous studies in model organisms have found complex and, at times contradictory, relationships among these genomic attributes highlighting the need to examine these patterns in other systems characterized by abundant sexual selection. Therefore, we examined the association among novel gene creation, tissue-specific gene expression, and chromosomal gene content within stalk-eyed flies. Flies in this family are characterized by strong sexual selection and the presence of a newly evolved X chromosome. We generated RNA-seq transcriptome data from the testes for three species within the family and from seven additional tissues in the highly dimorphic species, Teleopsis dalmanni. Analysis of dipteran gene orthology reveals dramatic testes-specific gene creation in stalk-eyed flies, involving numerous gene families that are highly conserved in other insect groups. Identification of X-linked genes for the three species indicates that the X chromosome arose prior to the diversification of the family. The most striking feature of this X chromosome is that it is highly masculinized, containing nearly twice as many testes-specific genes as expected based on its size. All the major processes that may drive differential sex chromosome gene content—creation of genes with male-specific expression, development of male-specific expression from pre-existing genes, and movement of genes with male-specific expression—are elevated on the X chromosome of T. dalmanni. This masculinization occurs despite evidence that testes expressed genes do not achieve the same levels of gene expression on the X chromosome as they do on the autosomes. © The Author 2016

Security System for Industrial Gate And Generation of Gate Pass

This paper gives description of face recognition system which automatically identifies and/or verifies the identity of a person from digital images. The basic flow of system is the image is captured by camera. The PCA algorithm detects the face and extracts its features. After the extraction, system compares the captured images with data base images. When the system found the person to be authorized then the system opens the gate automatically. But if the person is unauthorized then the system does not allow to entering in the industrial campus as well as it will generate the gate pass for the person

Evalution of normal CSF velocities at the level of aqueduct amongst Indian rural adults using 1.5 Tesla MRI

Rapid advances in imaging techniques have remarkably improved the diagnosis and treatment of central nervous system (CNS) disorders, with magnetic resonance imaging (MRI) being the most recent. New MRI applications are continually being developed, providing improved assessment of CNS disorders and their response to treatment, such as cerebrospinal fluid (CSF) movement, the alteration of which results in many clinical disorders with hydrocephalus (including normal pressure hydrocephalus), cystic CSF collections, and Chiari malformations being more common. CSF flow MRI can be used to discriminate between several disorders and provide information in the pre and postoperative evaluation of clinical disorders and surgical intervention. The aim of the study is to calculate and evaluate CSF flow velocities at the level of the aqueduct. MRI brain with CSF flow study was done in 40 patients. These patients were in the age group of 20-60 years and came with no significant clinical complaints. Phase contrast MRI scanning was used following the CSF quantitative flow protocol. A transverse single slice quantitative flow measurement was used to calculate the mean CSF flow velocity. Calculation of the CSF flow at the level of the cerebral aqueduct provides the best quantification of the CSF volume. It concluded that the normal range of the values of the CSF in normal individuals comes out to be 0.05 ±0.12 cm/sec