The evolution of altruism has been explained mainly from ultimate perspectives.
The joint success of these two closely interacting taxonomic groups has been explained by co-evolution [ 1- 4].
The evolution of the flow field for both configurations has been explained through phase-averaged measurements.
The diversity of the vacA genotype of H. pylori has been explained by a co-evolution model [21].
The long-term persistence of TEs in eukayotic genomes has been explained by models of selfish DNA evolution [2].
This observation has been explained by the model of horizontal or concerted evolution, originally proposed by Brown et al. [ 10].
The origin and evolution of Na HCO3 groundwater have been explained by many authors by combining various hydrogeochemical processes and water rock interaction reactions.
The evolutions of NW properties have been explained in detail.
The differences in the shape and evolution of the voltammograms during cycling have been explained by a different participation of the ions.
The differences in the shape and evolution of the voltammograms during cycling have been explained by the different participation of the ions in the redox-switching process.
