42 research outputs found
Workshop on Observations of Recent Comets (1990)
Potential interpretations are presented for observations of four comets: Brorsen-Metcalf (1989o), Okazaki-Levy-Rudenko (1989r), Aarseth-Brewington (1989a1), and Austin (1989o1). The relationship of minor species with each other and possible parents as well as with dust are being pursued in a number of investigations. Of particular interest are the abundance ratios of CH4 to CO and NH3 to N2. The need for closer collaboration betwen observing teams and modelers is examined. The need for dust size distribution as a function of cometocentric distance to be analyzed in closer collaboration between observers and modelers is discussed
A preliminary model of the coma of 2060 Chiron
We have included gravity in our fluid dynamic model with chemical kinetics of dusty comet comae and applied it with two dust sizes to 2060 Chiron. A progress report on the model and preliminary results concerning gas/dust dynamics and chemistry is given
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Energy balance and photochemical processes in the inner coma
Energy balance and multifluid flow in the coma are described. Expansion cooling, radiative cooling, photodissociative heating, chemical heating, and relative multifluid flow are the processes determining the energy budget. In the fluid dynamics, fast atomic and molecular hydrogen are considered as separate fluids with larger collision mean free paths than the cold bulk fluid that has a larger mean molecular weight. The transition from fluid flow to free molecular flow is approximated. The model predicts hydrogen and bulk fluid flow velocities in general agreement with observations. The effects of the temperature profile and the fast hydrogen flow on the chemistry in the inner coma are investigated. Results from a model approximating conditions in Halley's comet are presented
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients
Mutations in the filamin C gene (FLNC) cause a myofibrillar myopathy (MFM), morphologically characterized by focal myofibrillar destruction and abnormal accumulation of several proteins within skeletal muscle fibres. We studied 31 patients from four German families to evaluate the phenotype of filaminopathy. All patients harboured the same p.W2710X mutation in FLNC. Haplotype analysis suggested a founder mutation in these German filaminopathy families. The mean age at onset of clinical symptoms was 44 +/− 6 years (range, 24-57 years). Slowly progressive muscle weakness was mostly pronounced proximally, initially affecting the lower extremities and involving the upper extremities in the course of disease progression, similar to the distribution of weakness seen in limb-girdle muscular dystrophies (LGMD). Patients frequently developed respiratory muscle weakness. About one-third of the patients showed cardiac abnormalities comprising conduction blocks, tachycardia, diastolic dysfunction and left ventricular hypertrophy indicating a cardiac involvement in filaminopathy. Serum creatine kinase levels varied from normal up to 10-fold of the upper limit. Magnetic resonance imaging studies showed a rather homogenous pattern of muscle involvement in the lower extremities differing from that in other types of MFM. Myopathological features included perturbation of myofibrillar alignment, accumulation of granulofilamentous material similar to that seen in primary desminopathies and abnormal intracellular protein deposits typical of MFM. Decreased activities of oxidative enzymes and fibre hypertrophy seem to be early features, whereas dystrophic changes were present in advanced stages of filaminopathy. Rimmed vacuoles were detected in only a few cases. The intracellular aggregates were composed of a variety of proteins including filamin C, desmin, myotilin, Xin, dystrophin and sarcoglycans. Therapy is so far limited to symptomatic treatment. The German filaminopathy cohort, the largest group of patients studied so far, shares phenotypic features with LGMD and presents with characteristic histopathological findings of MF
Genome of Rhodnius prolixus, an insect vector of Chagas disease, reveals unique adaptations to hematophagy and parasite infection
Rhodnius prolixus not only has served as a model organism for the study of insect physiology, but also is a major vector of Chagas disease, an illness that affects approximately seven million people worldwide. We sequenced the genome of R. prolixus, generated assembled sequences covering 95% of the genome ( approximately 702 Mb), including 15,456 putative protein-coding genes, and completed comprehensive genomic analyses of this obligate blood-feeding insect. Although immune-deficiency (IMD)-mediated immune responses were observed, R. prolixus putatively lacks key components of the IMD pathway, suggesting a reorganization of the canonical immune signaling network. Although both Toll and IMD effectors controlled intestinal microbiota, neither affected Trypanosoma cruzi, the causal agent of Chagas disease, implying the existence of evasion or tolerance mechanisms. R. prolixus has experienced an extensive loss of selenoprotein genes, with its repertoire reduced to only two proteins, one of which is a selenocysteine-based glutathione peroxidase, the first found in insects. The genome contained actively transcribed, horizontally transferred genes from Wolbachia sp., which showed evidence of codon use evolution toward the insect use pattern. Comparative protein analyses revealed many lineage-specific expansions and putative gene absences in R. prolixus, including tandem expansions of genes related to chemoreception, feeding, and digestion that possibly contributed to the evolution of a blood-feeding lifestyle. The genome assembly and these associated analyses provide critical information on the physiology and evolution of this important vector species and should be instrumental for the development of innovative disease control methods
Differences between men and women in self-reported body mass index and its relation to drug use
Photodissociation and photoionisation of atoms and molecules of astrophysical interest
Opacity
The interaction of radiation with matter is a fundamental process in the universe; in particular, the absorption and scattering of radiation by matter (the opacity) govern the formation, evolution, and structure of stars and planets. But opacity is also important in many terrestrial applications in which radiation is the dominant means of energy transfer, such as controlled nuclear-fusion, laser ablation, atmospheric entry and reentry, and the "greenhouse" effect. This book covers all aspects of opacity and equations of state for plasmas, gases, vapors, and dust and emphasizes the continuous transformation of phases and molecular compositions with changing density and temperature under conditions of local thermodynamic equilibrium (LTE) while preserving the basic abundances of the chemical elements in a mixture
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Dust-Gas Interaction Deduced From Halley Multicolour Camera Observations
The dust and gas productions of Comet Halley were measured by the dust counter and the mass spectrometers on the Giotto spacecraft. These instruments give only little information about the spatial asymmetry of the activity. The asymmetry in the dust production is clearly evident from the dust jets seen in the Halley Multicolour Camera images. Since the dust is entrained by the gas, production must be similarly asymmetric. The intensity profiles along and across several dust jets are related to their source regions on the nucleus. Properties of the dust jets are investigated. A few compact, but highly active source regions on the nucleus produce most of the visible dust and can account for most of the gas produced by the comet. 2 refs