Gerald Mayr, Vanesa L. de Pietri, Leigh Love, Al A. Mannering, Joseph J. Bevitt and R. Paul Scofield (2020)
First Complete Wing of a Stem Group Sphenisciform from the Paleocene of New Zealand Sheds Light on the Evolution of the Penguin Flipper.
Diversity 12(2): 46
doi:
https://doi.org/10.3390/d12020046https://www.mdpi.com/1424-2818/12/2/46We describe a partial skeleton of a stem group penguin from the Waipara Greensand in New Zealand, which is tentatively assigned to Muriwaimanu tuatahi. The fossil includes the first complete wing of a Paleocene penguin and informs on previously unknown features of the mandible and tibiotarsus of small-sized Sphenisciformes from the Waipara Greensand. The wing is distinguished by important features from that of all geologically younger Sphenisciformes and documents an early stage in the evolution of wing-propelled diving in penguins. In particular, the wing of the new fossil exhibits a well-developed alular phalanx and the distal phalanges are not flattened. Because the wing phalanges resemble those of volant birds, we consider it likely that the wing feathers remained differentiated into functional categories and were not short and scale-like as they are in extant penguins. Even though the flippers of geologically younger penguins may favor survival in extremely cold climates, they are likely to have been shaped by hydrodynamic demands. Possible selective drivers include a diminished importance of the hindlimbs in subaquatic propulsion, new foraging strategies (the caudal end of the mandible of the new fossil distinctly differs from that of extant penguins), or increased predation by marine mammals.
Hui Wang, Hanbo Zhao, Keping Sun, Xiaobin Huang, Longru Jin & Jiang Feng (2020)
Evolutionary Basis of High-Frequency Hearing in the Cochleae of Echolocators Revealed by Comparative Genomics.
Genome Biology and Evolution 12(1): 3740â3753,
doi:
https://doi.org/10.1093/gbe/evz250https://academic.oup.com/gbe/article/12/1/3740/5626187High-frequency hearing is important for the survival of both echolocating bats and whales, but our understanding of its genetic basis is scattered and segmented. In this study, we combined RNA-Seq and comparative genomic analyses to obtain insights into the comprehensive gene _expression_ profile of the cochlea and the adaptive evolution of hearing-related genes. A total of 144 genes were found to have been under positive selection in various species of echolocating bats and toothed whales, 34 of which were identified to be related to hearing behavior or auditory processes. Subsequently, multiple physiological processes associated with those genes were found to have adaptively evolved in echolocating bats and toothed whales, including cochlear bony development, antioxidant activity, ion balance, and homeostatic processes, along with signal transduction. In addition, abundant convergent/parallel genes and sites were detected between different pairs of echolocator species; however, no specific hearing-related physiological pathways were enriched by them and almost all of the convergent/parallel signals were selectively neutral, as previously reported. Notably, two adaptive parallel evolved sites in TECPR2 were shown to have been under positive selection, indicating their functional importance for the evolution of echolocation and high-frequency hearing in laryngeal echolocating bats. This study deepens our understanding of the genetic bases underlying high-frequency hearing in the cochlea of echolocating bats and toothed whales.