ULTRACAM photometry of the eclipsing cataclysmic variable OU Vir

We present high-speed, three-colour photometry of the faint eclipsing cataclysmic variable OU Vir. For the first time in OU Vir, separate eclipses of the white dwarf and bright spot have been observed. We use timings of these eclipses to derive a purely photometric model of the system, obtaining a mass ratio of q = 0.175 +/- 0.025, an inclination of i = 79.2 +/- 0.7 degrees and a disc radius of Rd/a = 0.2315 +/- 0.0150. We separate the white dwarf eclipse from the lightcurve and, by fitting a blackbody spectrum to its flux in each passband, obtain a white dwarf temperature of T = 21700 +/- 1200 K and a distance of D = 650 +/- 210 pc. Assuming that the primary obeys the Nauenberg (1972) mass-radius relation for white dwarfs and allowing for temperature effects, we also find a primary mass Mw/Msun = 0.90 +/- 0.19, primary radius Rw/Rsun = 0.0097 +/- 0.0031 and orbital separation a/Rsun = 0.75 +/- 0.05.Comment: 8 pages LaTeX, 6 figures. Accepted by MNRAS; erratum added at end. Mon.Not.Roy.Astron.Soc. 347 (2004) 1173, erratum in pres

ULTRACAM photometry of the eclipsing cataclysmic variables XZ Eri and DV UMa

We present high-speed, three-colour photometry of the faint eclipsing cataclysmic variables XZ Eri and DV UMa. We determine the system parameters through two techniques: first, timings of the eclipse contact phases of the white dwarf and bright-spot using the derivative of the light curve; and secondly, a parameterized model of the eclipse fitted to the observed light curve by chi-squared minimisation. For both objects, we prefer the latter method, as it is less affected by photon noise and rapid flickering. For XZ Eri we obtain a mass ratio q = 0.1098 +/- 0.0017 and an orbital inclination i = 80.16 +/- 0.09 degrees. For DV UMa we derive figures of q = 0.1506 +/- 0.0009 and i = 84.24 +/- 0.07 degrees. The secondary star in XZ Eri has a very low mass Mr/Msun = 0.0842 +/- 0.0024, placing it close to the upper limit on the mass of a brown dwarf.Comment: 10 pages LaTeX, 5 figures. Accepted by MNRA

ULTRACAM photometry of the eclipsing cataclysmic variables GY Cnc, IR Com and HT Cas

We present high-speed, three-colour photometry of the eclipsing cataclysmic variables GY Cnc, IR Com and HT Cas. We find that the sharp eclipses in GY Cnc and IR Com are due to eclipses of the white dwarf. There is some evidence for a bright-spot on the edge of the accretion disc in GY Cnc, but not in IR Com. Eclipse mapping of HT Cas is presented which shows changes in the structure of the quiescent accretion disc. Observations in 2002 show the accretion disc to be invisible except for the presence of a bright-spot at the disc edge. 2003 observations, however, clearly show a bright inner disc and the bright-spot to be much fainter than in 2002. Although no outburst was associated with either set of quiescent observations, the system was similar to 0.6 mJy brighter in 2003, mainly due to the enhanced emission from the inner disc. We propose that these changes are due to variations in the mass-transfer rate from the secondary star and through the disc. The disc colours indicate that it is optically thin in both its inner and outer regions. We estimate the white dwarf temperature of HT Cas to be 15 000 +/- 1000 K in 2002 and 14 000 +/- 1000 K in 2003

Quantitative mapping of transcriptome and proteome dynamics during polarization of human iPSC-derived neurons

The differentiation of neuronal stem cells into polarized neurons is a well-coordinated process which has mostly been studied in classical non-human model systems, but to what extent these findings are recapitulated in human neurons remains unclear. To study neuronal polarization in human neurons, we cultured hiPSC-derived neurons, characterized early developmental stages, measured electrophysiological responses, and systematically profiled transcriptomic and proteomic dynamics during these steps. The neuron transcriptome and proteome shows extensive remodeling, with differential expression profiles of ~1100 transcripts and ~2200 proteins during neuronal differentiation and polarization. We also identified a distinct axon developmental stage marked by the relocation of axon initial segment proteins and increased microtubule remodeling from the distal (stage 3a) to the proximal (stage 3b) axon. This developmental transition coincides with action potential maturation. Our comprehensive characterization and quantitative map of transcriptome and proteome dynamics provides a solid framework for studying polarization in human neurons

Short timescale imaging polarimetry of geostationary satellite Thor-6: The nature of micro-glints

Large constellations of orbiting communication satellites will become an important source of noise for present and future astronomical observatories. Mitigation measures rely on high quality predictive models of the position and expected brightness of these objects. Optical linear imaging polarimetry holds promise as a quantitative tool to improve our understanding of the physics of reflection of sunlight off satellite components and through which models of expected brightness can be improved. We present the first simultaneous short-timescale linear polarimetry and optical photometry observations of a geostationary satellite, using the new MOPTOP imaging polarimeter on the 2 m Liverpool Telescope. Our target, telecommunication satellite Thor-6, shows prominent short timescale glint-like features in the lightcurve, some as short as seconds. Our polarimetric observations overlap with several of these micro-glints, and have the cadence required to resolve them. We find that the polarisation lightcurve is remarkably smooth, the short time scale glints are not seen to produce strong polarimetric features in our observation. We show how short timescale polarimetry can further constrain the properties of the components responsible for these micro-glints

Centrosome‐mediated microtubule remodeling during axon formation in human iPSC‐derived neurons

Axon formation critically relies on local microtubule remodeling and marks the first step in establishing neuronal polarity. However, the function of the microtubule-organizing centrosomes during the onset of axon formation is still under debate. Here, we demonstrate that centrosomes play an essential role in controlling axon formation in human-induced pluripotent stem cell (iPSC)-derived neurons. Depleting centrioles, the core components of centrosomes, in unpolarized human neuronal stem cells results in various axon developmental defects at later stages, including immature action potential firing, mislocalization of axonal microtubule-associated Trim46 proteins, suppressed expression of growth cone proteins, and affected growth cone morphologies. Live-cell imaging of microtubules reveals that centriole loss impairs axonal microtubule reorganization toward the unique parallel plus-end out microtubule bundles during early development. We propose that centrosomes mediate microtubule remodeling during early axon development in human iPSC-derived neurons, thereby laying the foundation for further axon development and function

Centrosome-mediated microtubule remodeling during axon formation in human iPSC-derived neurons

Axon formation critically relies on local microtubule remodeling and marks the first step in establishing neuronal polarity. However, the function of the microtubule-organizing centrosomes during the onset of axon formation is still under debate. Here, we demonstrate that centrosomes play an essential role in controlling axon formation in human-induced pluripotent stem cell (iPSC)-derived neurons. Depleting centrioles, the core components of centrosomes, in unpolarized human neuronal stem cells results in various axon developmental defects at later stages, including immature action potential firing, mislocalization of axonal microtubule-associated Trim46 proteins, suppressed expression of growth cone proteins, and affected growth cone morphologies. Live-cell imaging of microtubules reveals that centriole loss impairs axonal microtubule reorganization toward the unique parallel plus-end out microtubule bundles during early development. We propose that centrosomes mediate microtubule remodeling during early axon development in human iPSC-derived neurons, thereby laying the foundation for further axon development and function