Activity evolution, outbursts, and splitting events of comet 73P/Schwassmann-Wachmann 3

Context. The split Jupiter family comet 73P/Schwassmann-Wachmann 3 was monitored between January 21 and May 25 2006, for 24 nights. Aims. The goals of the campaign were to characterize the two principal comet components (C and B) and the smaller component G during their approach to perihelion, and study differences and commonalities in their evolution to obtain insight into the nature of the nuclei (gas and dust). We aimed to assess the chemical homogeneity/heterogeneity of the different components, the presence of jets and other coma structures, the rotation axis, the long-term activity evolution, and the detection of new fragmentation events. Methods. Long-slit spectra and optical broadband images were acquired using the CAFOS instrument at the 2.2-m telescope at Calar Alto Observatory (CSIC-MPG). Data obtained in service mode consisted of spectra and Johnson R filter images. By observing for four nights close to perigee, the comet could be imaged in the Johnson UBVRI filters. When possible, we analyzed the radial profile of the dust brightness and we derived the dust and gas production rates, the dust reddening, and the N-S profiles of the CN, C2, and C3 column densities. The analysis of the morphological evolution of coma structures and the determination of the rotation axis is performed in a separate paper. Results. We found that components C and B behave differently during most of our observations. While component C did not show any sudden increase in dust productivity, as measured by Afp, component B was characterized by a higher activity variation, exhibiting two outburst peaks and fragmentation events. Excluding outburst dates, component B always had lower dust productivity than component C. We also found differences in the behavior of the dust brightness radial profiles and in the dust colors. Differences in the dust colors are found also with respect to component G. In the spectral analysis, we found that both C and B components seem to be carbon-chain depleted, their compositions being almost the same. This indicates that the pre-split original, intact nucleus probably had a homogenous composition. A two-dimensional color map of component B on May 13 shows relative color variations in the inner coma that can be interpreted qualitatively in terms of Mie theory as fragmentation of silicate dust particles emanating from the nucleus. © ESO 2009

Coma structures in comet 73P/schwassmann-wachmann 3, components B and C, between january and may 2006

The Jupiter family comet 73P/Schwassmann-Wachmann 3 has been widely observed since 1995 after a nucleus break-up event produced at least five components labeled 73P-A to E. During the 2006 appearance, two of them (B and C) showed very strong coma activity. Our R-filter imaging of 73P-B & C from 21 January to 25 May 2006 revealed the presence of fan-like structures in the comae of both components and evidence for further fragmentation events in component B. As of early April 2006, component C showed two jets emanating from the nucleus, with one continuously visible. Through a simulation of the orbital geometry we infer that the rotation axis of 73P-C has an inclination of 20° to the orbital plane and a longitude of 45° at perihelion. The coma activity of component B was highly variable, displaying signatures of at least 3 fragmentation events. The coma was characterized by the continuous presence of a jet roughly in sunward direction, starting from the beginning of May. The first fragmentation event of component B may have happened between April 16 and April 26, leading to the presence of at least 6 fragments detected in images of May 2. The second one happened on or shortly before May 8, the third one between May 18 and 24. For the rotation axis of 73P-B we infer an inclination of 5°-15° to the orbital plane and a longitude of 20°-30° at perihelion. © 2009 Springer Science+Business Media B.V

Beauty in Disability: An Aesthetics for Dance and for Life

To what extent does dance contribute to an ideal of beauty that can enrich human quality of life? To what extent are standards of beauty predicated on an ideal human body that has no disability? In this chapter, we show how conceptions of proportionality, perfection, and ethereality from the Ancient Greeks through the 19th century can still be seen today in some kinds of dance, particularly in ballet. Disability studies and disability-inclusive dance companies, however, have started to change this. The disabled person can be beautiful, we will show, in dance and in life, under a disability aesthetics that follows Edmund Burke (1730-1797) and that suggests an alternative standard of beauty, which we call “beauty-in-experience,” where beauty is perceived in the qualitative experience of abled and disabled dancers moving together in dance.https://ecommons.udayton.edu/books/1023/thumbnail.jp

The Distribution, Excitation and Formation of Cometary Molecules: Methanol, Methyl Cyanide and Ethylene Glycol

We present an interferometric and single dish study of small organic species toward Comets C/1995 O1 (Hale-Bopp) and C/2002 T7 (LINEAR) using the BIMA interferometer at 3 mm and the ARO 12m telescope at 2 mm. For Comet Hale-Bopp, both the single-dish and interferometer observations of CH3OH indicate an excitation temperature of 105+/-5 K and an average production rate ratio Q(CH3OH)/Q(H2O)~1.3% at ~1 AU. Additionally, the aperture synthesis observations of CH3OH suggest a distribution well described by a spherical outflow and no evidence of significant extended emission. Single-dish observations of CH3CN in Comet Hale-Bopp indicate an excitation temperature of 200+/-10 K and a production rate ratio of Q(CH3CN)/Q(H2O)~0.017% at ~1 AU. The non-detection of a previously claimed transition of cometary (CH2OH)2 toward Comet Hale-Bopp with the 12m telescope indicates a compact distribution of emission, D<9'' (<8500 km). For the single-dish observations of Comet T7 LINEAR, we find an excitation temperature of CH3OH of 35+/-5 K and a CH3OH production rate ratio of Q(CH3OH)/Q(H2O)~1.5% at ~0.3 AU. Our data support current chemical models that CH3OH, CH3CN and (CH2OH)2 are parent nuclear species distributed into the coma via direct sublimation off cometary ices from the nucleus with no evidence of significant production in the outer coma.Comment: accepted for publication in Ap

Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker

Background: The molecular pathogenesis of T-cell large granular lymphocytic leukemia (T-LGLL), a mature T-cell leukemia arising commonly from T-cell receptor alpha beta-positive CD8(+) memory cytotoxic T cells, is only partly understood. The role of deregulated methylation in T-LGLL is not well known. We analyzed the epigenetic profile of T-LGLL cells of 11 patients compared to their normal counterparts by array-based DNA methylation profiling. For identification of molecular events driving the pathogenesis of T-LGLL, we compared the differentially methylated loci between the T-LGLL cases and normal T cells with chromatin segmentation data of benign T cells from the BLUEPRINT project. Moreover, we analyzed gene expression data of T-LGLL and benign T cells and validated the results by pyrosequencing in an extended cohort of 17 patients, including five patients with sequential samples. Results: We identified dysregulation of DNA methylation associated with altered gene expression in T-LGLL. Since T-LGLL is a rare disease, the samples size is low. But as confirmed for each sample, hypermethylation of T-LGLL cells at various CpG sites located at enhancer regions is a hallmark of this disease. The interaction of BLC11B and C14orf64 as suggested by in silico data analysis could provide a novel pathogenetic mechanism that needs further experimental investigation. Conclusions: DNA methylation is altered in T-LGLL cells compared to benign T cells. In particular, BCL11B is highly significant differentially methylated in T-LGLL cells. Although our results have to be validated in a larger patient cohort, BCL11B could be considered as a potential biomarker for this leukemia. In addition, altered gene expression and hypermethylation of enhancer regions could serve as potential mechanisms for treatment of this disease. Gene interactions of dysregulated genes, like BLC11B and C14orf64, may play an important role in pathogenic mechanisms and should be further analyzed

Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotency

The pathways involved in exit from pluripotency in human embryonic stem cells are poorly understood. Here, the authors performed a CRISPR-based screen to identify genes that promote exit from naïve pluripotency and find a role for folliculin (FLCN) by regulating the mTOR and Wnt pathways

Optimality of mutation and selection in germinal centers

The population dynamics theory of B cells in a typical germinal center could play an important role in revealing how affinity maturation is achieved. However, the existing models encountered some conflicts with experiments. To resolve these conflicts, we present a coarse-grained model to calculate the B cell population development in affinity maturation, which allows a comprehensive analysis of its parameter space to look for optimal values of mutation rate, selection strength, and initial antibody-antigen binding level that maximize the affinity improvement. With these optimized parameters, the model is compatible with the experimental observations such as the ~100-fold affinity improvements, the number of mutations, the hypermutation rate, and the "all or none" phenomenon. Moreover, we study the reasons behind the optimal parameters. The optimal mutation rate, in agreement with the hypermutation rate in vivo, results from a tradeoff between accumulating enough beneficial mutations and avoiding too many deleterious or lethal mutations. The optimal selection strength evolves as a balance between the need for affinity improvement and the requirement to pass the population bottleneck. These findings point to the conclusion that germinal centers have been optimized by evolution to generate strong affinity antibodies effectively and rapidly. In addition, we study the enhancement of affinity improvement due to B cell migration between germinal centers. These results could enhance our understandings to the functions of germinal centers.Comment: 5 figures in main text, and 4 figures in Supplementary Informatio

European consensus statement on essential colposcopy

Peer reviewedPostprin

Enabling the classroom and the curriculum: higher education, literary studies and disability

In this article the tripartite model of disability is applied to the lived experience of twenty-first-century higher education. The tripartite model facilitates a complex understanding of disability that recognises assumptions and discrimination but not at the cost of valued identity. This being so, not only the normative positivisms and non-normative negativisms but also the non-normative positivisms of the classroom and the curriculum are explored. Inclusion is taken as the starting point and the argument progresses to a profound and innovational appreciation of disability. The problem addressed is that inclusion, as shown in The Biopolitics of Disability, constitutes little more than inclusion-ism until disability is recognised in the context of alternative lives and values that neither enforce nor reify normalcy. Informed by this understanding, the article adopts the disciplinary example of literary studies and refers to Brian Friel’s Molly Sweeney as a primary text. The conclusion is that, despite passive and active resistance, disability enters higher education in many ways, most of which are beneficial to students and educators alike

Commentary on the WHO classification of tumors of lymphoid tissues (2008): aggressive B-cell lymphomas

In the novel WHO classification 2008, the classification of aggressive B-cell lymphoma has been revised for several categories with the aim to define “clean” entities. Within large B-cell lymphoma, a few distinct clinico-pathological entities have been recognized with more clinically defined entities than pathologically defined ones. The majority of known morphological variations were not considered to merit more than classification as a variant of DLBCL, not otherwise specified. Specifically, a biological subgrouping of DLBCL on the basis of molecular (activated B-cell versus germinal center B-cell) or immunophenotypic (CD5+) features was felt to be too immature to include at this stage. The role of EBV in aggressive B-cell lymphoma has been explored in more depth with the recognition of several novel and re-defined clinico-pathological entities. Also, in these diseases, clinical definitions play a very dominant role in the WHO classification 2008