albertonykus
Well-known member
Not strictly about paleontology, but they examine and discuss fossil feathers so may be of interest.
Chang, W.-L., H. Wu, Y.-K. Chiu, S. Wang, T.-X. Jiang, Z.-L. Luo, Y.-C. Lin, A. Li, J.-T. Hsu, H.-L. Huang, H.-J. Gu, T.-Y. Lin, S.-M. Yang, T.-T. Lee, Y.-C. Lai, M. Lei, M.-Y. Shie, C.-T. Yao, Y.-W. Chen, J.C. Tsai, S.-J. Shieh, Y.-K. Hwu, H.-C. Cheng, P.-C. Tang, S.-C. Hung, C.-F. Chen, M. Habib, R.B. Widelitz, P. Wu, W.-T. Juan, and C.-M. Chuong (2019)
The making of a flight feather: bio-architectural principles and adaptation
Cell 179: 1409-1423
doi: 10.1016/j.cell.2019.11.008
https://www.cell.com/cell/fulltext/S0092-8674%2819%2931229-2
The evolution of flight in feathered dinosaurs and early birds over millions of years required flight feathers whose architecture features hierarchical branches. While barb-based feather forms were investigated, feather shafts and vanes are understudied. Here, we take a multi-disciplinary approach to study their molecular control and bio-architectural organizations. In rachidial ridges, epidermal progenitors generate cortex and medullary keratinocytes, guided by Bmp and transforming growth factor β (TGF-β) signaling that convert rachides into adaptable bilayer composite beams. In barb ridges, epidermal progenitors generate cylindrical, plate-, or hooklet-shaped barbule cells that form fluffy branches or pennaceous vanes, mediated by asymmetric cell junction and keratin expression. Transcriptome analyses and functional studies show anterior-posterior Wnt2b signaling within the dermal papilla controls barbule cell fates with spatiotemporal collinearity. Quantitative bio-physical analyses of feathers from birds with different flight characteristics and feathers in Burmese amber reveal how multi-dimensional functionality can be achieved and may inspire future composite material designs.
Chang, W.-L., H. Wu, Y.-K. Chiu, S. Wang, T.-X. Jiang, Z.-L. Luo, Y.-C. Lin, A. Li, J.-T. Hsu, H.-L. Huang, H.-J. Gu, T.-Y. Lin, S.-M. Yang, T.-T. Lee, Y.-C. Lai, M. Lei, M.-Y. Shie, C.-T. Yao, Y.-W. Chen, J.C. Tsai, S.-J. Shieh, Y.-K. Hwu, H.-C. Cheng, P.-C. Tang, S.-C. Hung, C.-F. Chen, M. Habib, R.B. Widelitz, P. Wu, W.-T. Juan, and C.-M. Chuong (2019)
The making of a flight feather: bio-architectural principles and adaptation
Cell 179: 1409-1423
doi: 10.1016/j.cell.2019.11.008
https://www.cell.com/cell/fulltext/S0092-8674%2819%2931229-2
The evolution of flight in feathered dinosaurs and early birds over millions of years required flight feathers whose architecture features hierarchical branches. While barb-based feather forms were investigated, feather shafts and vanes are understudied. Here, we take a multi-disciplinary approach to study their molecular control and bio-architectural organizations. In rachidial ridges, epidermal progenitors generate cortex and medullary keratinocytes, guided by Bmp and transforming growth factor β (TGF-β) signaling that convert rachides into adaptable bilayer composite beams. In barb ridges, epidermal progenitors generate cylindrical, plate-, or hooklet-shaped barbule cells that form fluffy branches or pennaceous vanes, mediated by asymmetric cell junction and keratin expression. Transcriptome analyses and functional studies show anterior-posterior Wnt2b signaling within the dermal papilla controls barbule cell fates with spatiotemporal collinearity. Quantitative bio-physical analyses of feathers from birds with different flight characteristics and feathers in Burmese amber reveal how multi-dimensional functionality can be achieved and may inspire future composite material designs.