4 research outputs found

    Heat transfer in rapidly rotating convection with heterogeneous thermal boundary conditions

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    Convection in the metallic cores of terrestrial planets is likely to be subjected to lateral variations in heat flux through the outer boundary imposed by creeping flow in the overlying silicate mantles. Boundary anomalies can significantly influence global diagnostics of core convection when the Rayleigh number, Ra, is weakly supercritical; however, little is known about the strongly supercritical regime appropriate for planets. We perform numerical simulations of rapidly rotating convection in a spherical shell geometry and impose two patterns of boundary heat flow heterogeneity: a hemispherical Y¹₁ spherical harmonic pattern; and one derived from seismic tomography of the Earth’s lower mantle. We consider Ekman numbers 10⁻⁴ ≤E≤10⁻⁶, flux-based Rayleigh numbers up to 800 times critical, and a Prandtl number of unity. The amplitude of the lateral variation in heat flux is characterised by q^{∗}_{L} = 0, 2.3, 5.0, the peak-to-peak amplitude of the outer boundary heat flux divided by its mean. We find that the Nusselt number, Nu, can be increased by up to 25% relative to the equivalent homogeneous case due to boundary-induced correlations between the radial velocity and temperature anomalies near the top of the shell. The Nu enhancement tends to become greater as the amplitude and length scale of the boundary heterogeneity are increased and as the system becomes more supercritical. This Ra dependence can steepen the Nu α Ra^{γ} scaling in the rotationally dominated regime, with γ for our most extreme case approximately 20% greater than the equivalent homogeneous scaling. Therefore, it may be important to consider boundary heterogeneity when extrapolating numerical results to planetary conditions

    Data from: Inadvertent biological control: an Australian thrips killing an invasive New Zealand tree in California

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    Transport hubs of international trade and tourism are sites of unprecedented long-distance dispersal of species and novel ecological interactions. In cases of invasive plants released from their specialist natural enemies, novel interactions with both resident enemies and new arrivals can accumulate and potentially reduce weed competitiveness. I present here one dramatic example of this, where an invasive woody weed in southern California is being rapidly controlled by an accidentally introduced genus-specialist herbivorous insect. The New Zealand native shrub/small tree, Myoporum laetum, is a long-time popular ornamental plant in California and has become an invasive woody weed. In 2005, a Myoporum-specific thrips, Klambothrips myopori, was discovered (and described) in California feeding on M. laetum leaves. Several searches have failed to find K. myopori in New Zealand and a population has recently been discovered in Tasmania, Australia, feeding on Myoporum insulare. In 5 years, K. myopori has killed off about half of southern Californian M. laetum with almost all surviving individuals being gradually defoliated. Inadequate border biosecurity has resulted in inadvertent biological control, in a rapid timeframe, caused by a novel enemy. Unfortunately, K. myopori has subsequently been accidentally transported from California to Hawaii where it is now killing off Hawaiian native Myoporum sandwicense. Transport hubs can both connect weeds with natural enemies and disperse those enemies more widely
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