Assuming a neutral or nearly-neutral evolution of the mtDNA molecule, strong statistical support for post-glacial growth was seen for both A. alosa and A. fallax lineages in the Atlantic basin, with roughly similar age estimates, presumably reflecting expansion after the LGM (Table 6).
No one underlined this point more securely than Charles Darwin, who devised a theory of evolution that defied the strongest belief of his time, the all but universal belief in the bible version of the origins of man.
Experiments were conducted for lean and rich n-butane/air flames at 1atm initial pressure, demonstrating the complex and nonlinear nature of the dynamics of flame evolution, and the strong influences of the ignition transient and chamber confinement during the initial and final periods of the flame propagation, respectively.
We aim to explore the following questions: (1) Whether the subspecific patterns morphologically identified for the migratory locust in China are genetically supported; (2) How to explain the patterns in the context of biogeographic evolution, given the strong dispersal capabilities of the insect?
The evolution of the PSDF indicates a strong contribution to the mass of coagulation-mode by the nucleation-mode particles.
The case shows the chronic nature of the Toxocara invasion with the possibility of repeated relapses and wavy evolution of the disease, with a strong correlation between the intensity of invasion and clinical picture.
Alongside other reticulation phenomena, interspecific hybridization has played a key role in the evolution of the Triticeae, resulting in strong ecological, morphological and genetic similarities among many Triticeae taxa [ 14, 16, 82], notably with distinct gene lineages occurring within some polyploid as well as diploid species [ 83].
In fluorescence micrographs the evolution of a strong fluorescence emission along the crack planes is observed which can be related to the regeneration of the original anthracene groups in the damage-zone.
Third, the interaction of disruptive ecological selection and sexual selection for local adaptation does not suffer from one of the main obstacles to speciation: the evolution of sufficiently strong genetic associations between ecological and mating strategies (Arnegard and Kondrashov 2004; Gavrilets 2004; Bolnick and Fitzpatrick 2007).
But our results show that time evolution of the core flow leads to the strongest responses for the degrees more than triple of the maximum degree of the SV.
