Dwarf nova oscillations and quasi-periodic oscillations in cataclysmic variables – IV. Observations of frequency doubling and tripling in VW Hyi

We present new observations of the rapid oscillations in the dwarf nova VW Hyi, made late in outburst. These dwarf nova oscillations (DNOs) increase in period until they reach 33 s, when a transition to a strong 1st harmonic and weak fundamental takes place. After further period increase, the 2nd harmonic appears; often all three components are present simultaneously. This 1:2:3 frequency suite is similar to what has been seen in some neutron star and black hole X-ray binaries, but has not previously been seen in a cataclysmic variable. When studied in detail, the fundamental and 2nd harmonic vary similarly in phase, but the 1st harmonic behaves independently, though keeping close to twice the frequency of the fundamental. The fundamental period of the DNOs, as directly observed or inferred from the harmonics, increases to ∼100 s before the oscillation disappears as the star reaches quiescence. Its maximum period is close to that of the 'longer-period' DNOs observed in VW Hyi. The quasi-periodic oscillations (QPOs), which have fundamental periods 400–1000 s, behave in the same way, showing 1st and 2nd harmonics at approximately the same times as the DNOs. We explore some possible models. One in which the existence of the 1st harmonic is due to the transition from viewing a single accretion region to viewing two regions, and the rate of accretion on to the primary is modulated at the frequency of the 1st harmonic, as in the 'beat frequency model', can generate the suite of DNO frequencies observed. But the behaviour of the QPOs is not yet understood.     

The pillars of cosmology: a short history and assessment

Is the big bang model of the universe ascendant and unshakable, or declining and outdated? This paper cursorily explores the state of cosmology today.     

Damage due to ultraviolet and ionizing radiation during the ejection of shielded micro-organisms from the vicinity of 1M ⊙ main sequence and red giant stars

We present the astrophysical conditions necessary for the ejection of shielded microorganisms from a solar system and the biological conditions involving ultraviolet and ionizing radiations to which they are subjected in space. The radiation dose for both UV and ionizing radiation from the host star, the destination star and interstellar space is calculated for three different micro-organisms. The time of transport and the survival of the micro-organisms are strongly dependent on the composition and thickness of any mantle encasing the micro-organism and on the mass/luminosity ratio of the two stars. The maximum size of grains that can be ejected from the vicinity of one solar mass main sequence and red giant stars ranges from 0.65-0.35µm and 2.1-1.2µm respectively, for a reasonable range of densities. We conclude that unshielded known micro-organisms are immediately killed by ultraviolet radiation, and that an ice mantle does not provide sufficient shielding for either type of star. However, micro-organisms shielded by a carbonaceous thin-film mantle can be ejected from the vicinity of a one solar-mass red-giant star, and such micro-organisms have a high probability of surviving damage from the ultraviolet and ionizing radiations to which they are exposed.     

BV centauri: dwarf or classical nova?

The similarity in properties of GK Per and BV Cen suggests that the latter may be a classical nova remnant rather than a dwarf nova. Our H and V CCD photometry show no sign of a nova shell but disclose the presence of a close and probably physical companion. BV(RI) _c CCD photometry of the companion, assumed to be a dwarf, givesM _v =3.1±0.3 for BV Cen at quiescence. Even though half of the light in BV Cen comes from the secondary this is much brighter than expected for a dwarf nova and supports the conclusion that BV Cen was an unrecorded nova.     

Observation of clouds and solar radiation over the Pacific Ocean as relation to global climate

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Vertical migration and mortality of benthos in dredged material: Part III—polychaeta

The survival of benthic invertebrates from dredging and disposal activities is a major environmental concern in such projects. The purpose of the research described in this paper was to determine the ability of benthos (polychaetes, Scoloplos fragilis and Nereis succinea) to migrate vertically in natural and exotic sediments and to determine the survival of benthos when exposed to particular amounts of simulated dredged material.Mortalities generally increased with increased sediment depth, exotic sediment and burial time. Temperature also affected vertical migration and mortalities. These experiments, together with other experiments conducted by us and other workers, indicate that polychaetes in particular, and benthos in general, can survive dredging and disposal projects. Under certain conditions several major taxa (polychaetes, molluscs, crustaceans) can be expected to successfully recolonise disposal sites by vertical migration.     

Abundance of the introduced seastar, Asterias amurensis, and spatial variability in soft sediment assemblages in SE Tasmania: Clear correlations but complex interpretation

The northern Pacific seastar, Asterias amurensis, was first collected in southeast Tasmania in 1986. Mistaken for the endemic asteroid Uniophora granifera, its true identity was not realised until 1992. It is now a conspicuous predator in soft sediment habitats in this region, and is considered a major threat to native assemblages and commercial species. We examined the structure of soft sediment assemblages at different spatial scales in southeast Tasmania, and correlated spatial variation in community composition with seastar abundances. We found that the structure of soft sediment assemblages is highly variable at a range of spatial scales from metres to tens of kilometres. Clear differences in the composition of assemblages and abundances of major taxa were detected between areas with and without seastars and between areas with low and high seastar densities. However, the nature of these patterns suggests that they are more likely due to differences in sediment characteristics than due to impacts of the seastar. Thus, spatial differences in soft sediment assemblages might have been erroneously attributed to seastars without detailed information on important physical factors such as sediment characteristics. A second survey, using larger sampling units (1 m²) but across a more limited spatial extent, targeted bivalves and heart urchins that were identified as important prey of the seastar in observations of feeding and in experimental studies. Large-scale patterns of abundance and size structure were consistent with seastar effects anticipated from small-scale experimental and feeding studies for some, but not all, species. While the field survey ultimately provided evidence about the presence or absence of seastar impacts at large-scales, the identification of key ecological variables in experimental and feeding studies proved crucial to both the design and interpretation of patterns observed in the large-scale surveys. Overall, this work highlighted the necessity to consider multiple lines of evidence rather than relying on a single ‘inferential’ test, in the absence of pre-impact data.