19 research outputs found

    Size and Shape of Chariklo from Multi-epoch Stellar Occultation

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    We use data from five stellar occultations observed between 2013 and 2016 to constrain Chariklo’s size and shape, and the ring reflectivity. We consider four possible models for Chariklo (sphere, Maclaurin spheroid, triaxial ellipsoid, and Jacobi ellipsoid), and we use a Bayesian approach to estimate the corresponding parameters. The spherical model has a radius R = 129 ± 3 km. The Maclaurin model has equatorial and polar radii a=b={143}-6+3 {km} and c={96}-4+14 {km}, respectively, with density {970}-180+300 {kg} {{{m}}}-3. The ellipsoidal model has semiaxes a={148}-4+6 {km}, b={132}-5+6 {km}, and c={102}-8+10 {km}. Finally, the Jacobi model has semiaxes a = 157 ± 4 km, b = 139 ± 4 km, and c = 86 ± 1 km, and density {796}-4+2 {kg} {{{m}}}-3. Depending on the model, we obtain topographic features of 6–11 km, typical of Saturn icy satellites with similar size and density. We constrain Chariklo’s geometric albedo between 3.1% (sphere) and 4.9% (ellipsoid), while the ring I/F reflectivity is less constrained between 0.6% (Jacobi) and 8.9% (sphere). The ellipsoid model explains both the optical light curve and the long-term photometry variation of the system, giving a plausible value for the geometric albedo of the ring particles of 10%–15%. The derived mass of Chariklo of 6–8 × 1018 kg places the rings close to 3:1 resonance between the ring mean motion and Chariklo’s rotation period

    Intra- and intermale variability of mature sperm traits analysed in two brackish water populations of the pipefish Syngnathus abaster (Syngnathidae)

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    Sperm cells are highly diversified in animals, and considerable research effort has focused on variation in sperm morphology among species. Surprisingly, little is known about intraspecific variation in sperm morphology. We analysed within- and between-male variation in mature sperm traits in two brackish water populations of the pipefish Syngnathus abaster. Four morphometric parameters, such as the width and length of the head (including nucleus, and midpiece), length of flagellum and total sperm length were taken into account. The differences in all morphometric parameters analysed between populations were not statistically significant. Moreover, the multidimensional scaling analysis shows that (i) the two populations seem to be indistinguishable based on their spermatozoa and (ii) there is not polymorphism, being sperm not distinguishable into discrete classes both within a single male and between males of each populations. The latter datum does not seem to support the presence of polymorphic sperm in syngnathids. Both populations, however, exhibit a high variation in all sperm traits, both among individual sperm within an ejaculate and among males within each population. The relationship between sperm traits variability and the low selection pressure determined by the absence of postcopulatory sexual selection (i.e. absence of sperm competition) is discussed
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