Line width distributions as evidence for axisymmetry in the broad line regions of active galaxies

The nuclei of a wide class of active galaxies emit broad emission lines with widths at half maximum (FWHM) in the range $10^{3}-10^{4}$ km s$^{-1}$. This spread of widths is not solely a consequence of the range of the luminosities of these sources since a plot of width versus luminosity shows a large scatter. We propose that the broad line emission region (BLR) is axially symmetric and that this scatter in line width arises from an additional dependence on the angle of the line of sight to the axis of the emission region. Such a relation is natural in unified models of active nuclei which link a variety of observed properties to viewing angle. Adopting a simple form for the line width as a function of luminosity and angle, and convolving this with the observed luminosity function, allows us to predict a line width distribution consistent with the available data. Furthermore, we use the relation between the equivalent width of a line and the luminosity in the continuum (the `Baldwin Effect') to predict an observed correlation between line width and equivalent width. The scatter on this correlation is again provided by angular dependence. The results have applications as diagnostics of models of the broad line emission region and in cosmology.Comment: 8 pages including 4 figures. Accepted for publication in MNRAS Letter

The luminosity dependence of opening angle in unified models of active galaxies

In unified models of active galaxies the direct line of sight to the nucleus is unobscured only within a certain cone of directions. An opening angle for this cone is usually estimated by methods such as the overall ratio of Seyfert 1s to Seyfert2s, the latter assumed to be obscured versions of the former. Here we shall show, as has often been suspected, that the opening angle of the cone depends on the luminosity of the central source, with higher luminosities corresponding to larger opening angles. This conclusion depends only on the assumption that the width of the broad emission lines at a given luminosity is a measure of inclination angle, an assumption that is supported by observation in radio-loud systems. On the other hand we show that the scatter in X-ray spectral index is not primarily an effect of viewing angle, in contrast to what might be expected if the scatter on the spectral index versus luminosity relation were a consequence of absorption in the obscuring material. The observed correlation between linewidth and spectral index appears to be a further consequence of the dependence of opening angle on luminosity.Comment: 8 pages, 7 figures, uses mn.sty. Accepted for publication in MNRA

Determining the cosmological parameters from the linewidths of active galaxies

We have previously shown that the linewidth distribution in AGN can be accounted for by an axisymmetric broad emission line region. In this paper we show that the linewidth distribution changes with redshift and that these changes are dependent on H_0 and q_0. We show that relatively small samples of AGN at high redshift with measured linewidth at half maximum can be used to distinguish between values of H_0 and q_0. Furthermore larger low redshift samples can be used to distinguish between luminosity functions and hence different models of quasar evolution.Comment: Accepted for publication in MNRAS. 8 pages LaTeX, uses mn.st

Changing teaching techniques and adapting new technologies to improve student learning in an introductory meteorology and climate course

Responding to the call for reform in science education, changes were made in an introductory meteorology and climate course offered at a large public university. These changes were a part of a larger project aimed at deepening and extending a program of science content courses that model effective teaching strategies for prospective middle school science teachers. Therefore, revisions were made to address misconceptions about meteorological phenomena, foster deeper understanding of key concepts, encourage engagement with the text, and promote inquiry-based learning. Techniques introduced include: use of a flash cards, student reflection questionnaires, writing assignments, and interactive discussions on weather and forecast data using computer technology such as Integrated Data Viewer (IDV). The revision process is described in a case study format. Preliminary results (self-reflection by the instructor, surveys of student opinion, and measurements of student achievement), suggest student learning has been positively influenced. This study is supported by three grants: NSF grant No. 0202923, the Unidata Equipment Award, and the Lucia Harrison Endowment Fund

Cognitive decline heralds onset of symptomatic inherited prion disease

The clinical effectiveness of any disease-modifying treatment for prion disease, as for other neurodegenerative disorders, will depend on early treatment before damage to neural tissue is irrevocable. Thus, there is a need to identify markers which predict disease onset in healthy at-risk individuals. Whilst imaging and neurophysiological biomarkers have shown limited use in this regard, we recently reported progressive neurophysiological changes in healthy people with the inherited prion disease mutation P102L (Rudge et al, Brain 2019). We have also previously demonstrated a signature pattern of fronto-parietal dysfunction in mild prion disease (Caine et al., 2015; 2018). Here we address whether these cognitive features anticipate the onset of symptoms in a unique sample of patients with inherited prion disease. In the cross-sectional analysis, we analysed the performance of patients at three time points in the course of disease onset: prior to symptoms (n = 27), onset of subjective symptoms without positive clinical findings (n = 8) and symptomatic with positive clinical findings (n = 24). In the longitudinal analysis, we analysed data from twenty four patients who were presymptomatic at the time of recruitment and were followed up over a period of up to seventeen years, of whom sixteen remained healthy and eight converted to become symptomatic. In the cross-sectional analysis, the key finding was that, relative to a group of 25 healthy non-gene carrier controls, patients with subjective symptoms but without positive clinical findings were impaired on a smaller but very similar set of tests (Trail Making Test part A, Stroop Test, Performance IQ, gesture repetition, figure recall) to those previously found to be impaired in mild prion disease (Caine et al., 2015; 2018). In the longitudinal analysis, Trail Making Test parts A and B, Stroop test and Performance IQ scores significantly discriminated between patients who remained presymptomatic and those who converted, even before the converters reached criteria for formal diagnosis. Notably, performance on the Stroop test significantly discriminated between presymptomatic patients and converters before the onset of clinical symptoms (AUC = .83 (95% CI, 0.62-1.00), p =.009). Thus, we report here, for the first time, neuropsychological abnormalities in healthy patients prior to either symptom onset or clinical diagnosis of IPD. This constitutes an important component of an evolving profile of clinical and biomarker abnormalities in this crucial group for preventive medicine

Combined^147,146Sm-^143,142Nd constraints on the longevity and residence time of early terrestrial crust

Primordial silicate differentiation controlled the composition of Earth's oldest crust. Inherited 142Nd anomalies in Archean rocks are vestiges of the mantle-crust differentiation before ca. 4300 Ma. Here we report new whole-rock 147,146Sm-143,142Nd data for the Acasta Gneiss Complex (AGC; Northwest Territories, Canada). Our 147Sm-143Nd data combined with literature data define an age of 3371 ± 141 Ma (2 SD) and yield an initial ε143Nd of −5.6 ± 2.1. These results are at odds with the Acasta zircon U-Pb record, which comprises emplacement ages of 3920–3960 Ma. Ten of our thirteen samples show 142Nd deficits of −9.6 ± 4.8 ppm (2 SD) relative to the modern Earth. The discrepancy between 142Nd anomalies and a mid-Archean 147Sm-143Nd age can be reconciled with Nd isotope reequilibration of the AGC during metamorphic perturbations at ca. 3400 Ma. A model age of ca. 4310 Ma is derived for the early enrichment of the Acasta source. Two compositional end-members can be identified: a felsic component with 142Nd/144Nd identical to the modern Earth and a mafic component with 142Nd/144Nd as low as −14.1 ppm. The ca. 4310 Ma AGC source is ∼200 Myr younger than those estimated for Nuvvuagittuq (northern Québec) and Isua (Itsaq Gneiss Complex, West Greenland). The AGC does not have the same decoupled Nd-Hf isotope systematics as these other two terranes, which have been attributed to the crystallization of an early magma ocean. The Acasta signature rather is ascribed to the formation of Hadean crust that was preserved for several hundred Myr. Its longevity can be linked to 142Nd evolution in the mantle and does not require slow mantle stirring times nor modification of its convective mode.This project was funded by an ETH internal grant to BB. We thank Colin Maden for maintenance of the mass spectrometer. SJM acknowledges support from the NASA Exobiology and Evolutionary Biology Program (Investigating the Hadean Earth) and the NASA Lunar Science Institute (Center for Lunar Origin and Evolution, CLOE). Additional support to SJM came from the Laboratoire de Géologie de Lyon, Université Claude Bernard Lyon 1, and a Distinguished Professorship awarded by the Hungarian Academy of Sciences. JBT received support from the French Agence Nationale de la Recherche (Grant ANR-10-BLAN-0603 M&Ms — Mantle Melting — Measurements, Models, Mechanisms).This is the version of record, which can also be found on the publisher's website at: http://onlinelibrary.wiley.com/doi/10.1002/2014GC005313/abstract © 2014. American Geophysical Union. All Rights Reserved

Volumetric Absorptive Microsampling (VAMS) for Targeted LC-MS/MS Determination of Tryptophan-Related Biomarkers

L-Tryptophan (TRP) metabolites and related biomarkers play crucial roles in physiological functions, and their imbalances are implicated in central nervous system pathologies and neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), Alzheimer's disease, Parkinson's disease, schizophrenia and depression. The measurement of TRP metabolites and related biomarkers possesses great potential to elucidate the disease mechanisms, aid preclinical drug development, highlight potential therapeutic targets and evaluate the outcomes of therapeutic interventions. An effective, straightforward, sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the simultaneous determination of 24 TRP-related compounds in miniaturised murine whole blood samples. Sampling and sample pretreatment miniaturisation were achieved thanks to the development of a volumetric dried blood microsampling approach. Volumetric absorptive microsampling (VAMS) allows the accurate sampling of microvolumes of blood with advantages including, but not limited to, minimal sampling invasiveness, logistical improvements, method sustainability in terms of solvents and energy consumption, and improvement of animal studies in the framework of the 3Rs (Replacement, Reduction and Refinement) principles on animal welfare. The VAMS-LC-MS/MS method exhibited good selectivity, and correlation coefficient values for the calibration curves of each analyte were >0.9987. The limits of quantitation ranged from 0.1 to 25 ng/mL. The intra- and inter-day precisions in terms of RSD were <9.6%. All analytes were stable in whole blood VAMS samples stored at room temperature for at least 30 days with analyte losses < 14%. The developed method was successfully applied to the analysis of biological samples from mice, leading to the unambiguous determination of all the considered target analytes. This method can therefore be applied to analyse TRP metabolites and related biomarkers levels to monitor disease states, perform mechanistic studies and investigate the outcomes of therapeutic interventions

Inhibition of delta-like ligand 4 induces luteal hypervascularization followed by functional and structural luteolysis in the primate ovary

Using specific inhibitors established that angiogenesis in the ovarian follicle and corpus luteum is driven by vascular endothelial growth factor. Recently, it has been demonstrated that the Notch ligand, delta-like ligand 4 (Dll4) negatively regulates vascular endothelial growth factor-mediated vessel sprouting and branching. To investigate the role of Dll4 in regulation of the ovarian vasculature, we administered a neutralizing antibody to Dll4 to marmosets at the periovulatory period. The vasculature was examined on luteal d 3 or d 10: angiogenesis was determined by incorporation of bromodeoxyuridine, staining for CD31 and cell death by staining for activated caspase-3. Ovulatory progesterone rises were monitored to determine effects of treatment on luteal function and time to recover normal cycles in a separate group of animals. Additionally, animals were treated in the follicular or midluteal phase to determine effects of Dll4 inhibition on follicular development and luteal function. Controls were treated with human IgG (Fc). Corpora lutea from marmosets treated during the periovulatory period exhibited increased angiogenesis and increased vascular density on luteal d 3, but plasma progesterone was significantly suppressed. By luteal d 10, corpora lutea in treated ovaries were significantly reduced in size, with involution of luteal cells, increased cell death, and suppressed plasma progesterone concentrations. In contrast, initiation of anti-Dll4 treatment during the midluteal phase produced only a slight suppression of progesterone for the remainder of the cycle. Moreover, Dll4 inhibition had no appreciable effect on follicular development. These results show that Dll4 has a specific and critical role in the development of the normal luteal vasculature

Ethics, space, and somatic sensibilities: comparing relationships between scientific researchers and their human and animal experimental subjects

Drawing on geographies of affect and nature-society relations, we propose a radical rethinking of how scientists, social scientists, and regulatory agencies conceptualise human and animal participants in scientif ic research. The scientific rationale for using animal bodies to simulate what could be done in human bodies emphasises shared somatic capacities that generate comparable responses to clinical interventions. At the same time, regulatory guidelines and care practices stress the differences between human and animal subjects. In this paper we consider the implications of this differentiation between human and animal bodies in ethical and welfare protocols and practices. We show how the bioethical debates around the use of human subjects tend to focus on issues of consent and language, while recent work in animal welfare reflects an increasing focus on the affectual dimensions of ethical practice. We argue that this attention to the more-than-representational dimensions of ethics and welfare might be equally important for human subjects. We assert that paying attention to these somatic sensibilities can offer insights into how experimental environments can both facilitate and restrict the development of more care-full and response-able relations between researchers and their experimental subjects. <br/

A Pair Polarimeter for Linearly Polarized High Energy Photons

A high quality beam of linearly polarized photons of several GeV will become available with the coherent bremsstrahlung technique at JLab. We have developed a polarimeter which requires about two meters of the beam line, has an analyzing power of 20% and an efficiency of 0.02%. The layout and first results of a polarimeter test on the laser back-scattering photon beam at SPring-8/LEPS are presented