Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Archaeopteryx feather sheaths reveal sequential center-out flight-related molting strategy


Modern flying birds molt to replace old and worn feathers that inhibit flight performance, but its origins are unclear. We address this by presenting and evaluating a ~150 million year old record of molting in a feathered dinosaur from the early bird Archaeopteryx. Laser-Stimulated Fluorescence revealed feather sheaths that are otherwise invisible under white light. These are separated by one feather and are not in numerical sequential order and are mirrored in both wings. This indicates that a sequential center-out molting strategy was already present at the origins of flight, which is used in living falcons to preserve maximum flight performance. This strategy would have been a welcome advantage for early theropod flyers that had poor flight capabilities. This discovery provides important insights into how birds refined their early flight capabilities before the appearance of the keeled sternum, pygostyle and triosseal canal.


Modern flying birds molt in a variety of ways with the goal of replacing old and worn feathers that inhibit flight performance1,2. Molting is often constrained by feather growth because its rate has a narrow range that does not scale with feather size3. Feather growth rates for smaller or larger birds are typically between 3.2 and 6.3 mm per day for primary feathers3. For smaller birds with correspondingly smaller feathers, the remiges can grow out in a single season, leading to complete replacement3. Larger birds tend toward partial molts known as Staffelmauser so complete replacement extends over several seasons3,4.

The most common molting strategy is a sequential molt, where feathers are lost from the left and right wing at the same time and proceed in a symmetrical pattern4. The sequence of feather loss itself has two strategies. The first strategy is a numerically sequential molt where feathers are lost in numerical order and is the most common among passerines. Typically, the primary feather molt proceeds from the innermost feather sequentially outwards to the tip3. The second strategy is a center-out approach where a center feather is lost first and then subsequent feathers are shed outwards from this center point; this is more common in non-passerine birds such as falcons5. This minimizes the size of the aerodynamic hole in the wing, which allows falcons to better maintain their flight performance for hunting3,6.

Pennaraptorans are the group of theropod dinosaurs that generically have vaned feathers and include birds7. They also comprise oviraptorosaurians and the closest bird relatives, the dromaeosaurids and troodontids. We define birds in this study as Avialae Gauthier 1986, a stem-based taxon containing Passer domesticus Linnaeus, 1758, and all coelurosaurian theropods closer to it than to Dromaeosaurus albertensis Matthew and Brown, 1922, or Troodon formosus Leidy, 1856 (sensu7,8,9). The ancestral feathered pennaraptoran did not fly7, so its feathers would not have molted due to flight performance pressure and presumably did so non-systematically. Among early fossil pennaraptorans, molting has only been identified in the Early Cretaceous flying dromaeosaurid Microraptor10,11. The authors observed a sequential molt strategy, but did not explicitly state which specific sequential strategy was involved: numerical or center out. The authors based this interpretation on the feather gap in the wing of specimen IVPP V13352 and three primary feathers that decrease in length outwards10. As the feathers are changing length in a numerical sequence, this suggests that Microraptor adopted a numerically sequential molting strategy. The sequential molt in Microraptor and molting data in extant birds was used by Kiat et al.10 to suggest that sequential molting is the outcome of evolutionary forces to maintain flight capability throughout the entire annual cycle in both extant birds and non-avialan paravian theropods10. Although it was not stated in their study, the ancestral molting condition for Paraves is presumably numerically sequential molting.

Archaeopteryx from the Late Jurassic Solnhofen Limestones of southern Germany is currently considered the oldest undisputed fossil bird and is iconic in our understanding of avian origins and of evolution more generally12. The Thermopolis specimen of Archaeopteryx WDC-CSG-100 (Wyoming Dinosaur Center)13,14 was scanned under Laser-Stimulated Fluorescence (LSF)15 (see Methods). This revealed anatomy not seen in normal light. In this study we identify the earliest evidence of pennaraptoran feather molting to our knowledge and discuss its implications on the origins of flight-related molting and of flight.

Results and discussion

WDC-CSG-100 exhibited matching elements on both wings under Laser-Stimulated Fluorescence (LSF) imaging (Fig. 1). These elements were found at the proximal ends of the rachises of the middle primary feathers. Unlike the absence of a UV or LSF reaction by the feather calami in the Berlin (MB.Av.101), Eichstätt (JME 2257), Solnhofen (BMMS 500), Munich (BSP 1999 I 50), and eleventh (no. 02923) specimens of Archaeopteryx12,16,17,18,19, the reaction of the matched elements in WDC-CSG-100 under LSF (Fig. 1) rejects the hypothesis that the elements are unusually thickened feather calami made of keratin.

Fig. 1: Bilaterally symmetrical cornified feather sheaths on the wings of Archaeopteryx under LSF.

Molting feathers matched on both wings of WDC-CSG-100 ensured balanced aerodynamic performance. The white arrows indicate the feather sheaths. Scale bar is 1 cm.

Cornified feather sheaths encase the proximal end of new feathers during the growth phase, which fits the shape and position of the matching elements. The feather follicle embedded in the dermis, initially surrounds the developing feather filament20. The center of the filament contains the blood supply that feeds the growing feather20. The outer filament has three layers, the inner two form the feather proper while the outer most layer forms a keratinous sheath20. Once the feather has finished growing, the sheath dries up and falls off or is preened out. Thus, the matching elements could be molting feather sheaths.

The remaining possibility for stick-like elements in the same part of the pennaraptoran wing are bony extensions like the ‘styliform’ elements of the membrane-winged scansoriopterygids21,22. However, examination of the calcium elemental map produced from the SLAC National Accelerator Laboratory beamline23 (Fig. 2) showed a lack of calcium in these elements which rules this hypothesis out.

Fig. 2: Comparison of preserved organic tissues in Solnhofen fossils.

a Feather sheath from WDC-CSG-100. b Skin preservation on Juravenator JME Sch 200 (Jura Museum Eichstätt). c Wing membrane preserved in an undescribed pterosaur from the Jura Museum Eichstätt (JME SOS 2016). Scale bars: a, 0.5 cm, b 4 mm, and c 1 cm.

Remnant elemental signatures of skin are uncommon in the Solnhofen fossil record but examples such as the non-avialan theropod Juravenator and several pterosaurs (Fig. 2) show such signatures under LSF and ultra violet (UV) light24,25. The matching elements fluoresce like preserved skin in other Solnhofen fossils indicating that they are not bone. This supports the remaining hypothesis that the matching elements are epithelial feather sheaths made up of cornified cellular tissue26. This is also congruent with the lack of calcium in the SLAC elemental analysis23 (Fig. 2). Cornified tissue was previously detected under LSF with a similar fluorescence signature in the tail bristles of the ornithischian dinosaur Psittacosaurus27,28.

Figure 3 shows the two wings of WDC-CSG-100 side by side demonstrating paired symmetry of the fifth primaries. In Fig. 3a, arrow P7 identifies the remnant of a third sheath that is not paired on the opposite wing. These elements are not visible on the slab under white light or on other Archaeopteryx specimens imaged using LSF. The two elements are bilaterally symmetrical as would be expected from what is observed in modern molting pairs. The elements exhibit matching widths and lengths and stop short of contacting the bone as would be expected if they were anchored into the patagia as in modern birds. The sheaths center on the axis of the rachis as shown in the phosphorous distribution map from the Bergmann et al.23 SLAC image (Fig. 1). This sheath alignment rules out their association with molting primary covert feathers.

Fig. 3: Close up of the hands of WDC-CSG-100 under LSF showing the position of the bilaterally symmetrical cornified feather sheaths.

a Arrow P5a is the feather sheath on the fifth right primary feather. Arrow P7 shows remnants of the third sheath on the seventh primary feather. The sixth primary feather has already molted out and the molt sequence is proceeding in two opposite directions. b Arrow P5b points to the feather sheath on the fifth left primary feather which matches the one preserved on the right hand (arrow P5a). Scale bars are 0.5 cm.

The feather outlines on the right wing shows that the feathers were grown out and the feather sheaths were starting the process of being shed (Fig. 4). The primary count of 1113 suggests that a sequential “center out” molting strategy would start with either the fifth or sixth primary feather as the central vane from which to start the molt. The detection of feather sheaths one feather apart, suggests that the molt started with the sixth primary feather and proceeded out to the fifth and seventh which preserve the structures. This matches the modern sequential “center out” molting strategy that maintains maximum flight potential6. The symmetrical loss of the primary feathers balances the wing aerodynamics during the molt and maintains the best possible control when dealing with aerodynamically degraded wings6.

Fig. 4: Right wing of WDC-CSG-100 under white raking light showing numbered primary feathers.

Arrow delimiting the full length of a molted feather in WDC-CSG-100. This figure shows that primaries #5 and #7 were nearly full length. Cornified feather sheaths on primaries #5 and #7 are visible under LSF in Fig. 3a. The numbering on the feathers follows Mayr et al.13. The image is in grayscale and under white raking light to make the feathers easier to see. Scale bar is 2 cm.


The sequential “center out” molting strategy described here in Archaeopteryx is at least 150 million years old. To the best of our knowledge, this discovery is the oldest record of pennaraptoran feather molting (~25 million years older than the sequential molting record in Microraptor10) and the only record of adult molting in an early fossil bird (at least 20 million years older than existing avialan records from juvenile specimens from Spain and China29). Vaned feathers first evolved in pennaraptoran dinosaurs that could not fly17. This included asymmetrically vaned feathers that were traditionally associated with flight capability30. Thus, there was no original evolutionary pressure for a specific type of flight-related molting strategy, so molting presumably happened in a non-systematic manner early on. Asymmetrically vaned feathers were rapidly co-opted into the wings of early birds for powered flight30. A molting strategy that could maintain flight performance would have been a welcome advantage for early theropod flyers which had relatively poor flight capabilities11. Among early fossil pennaraptorans, numerically sequential molting has only been found in non-avialan pennaraptorans10. However, its prevalence among modern birds10 suggests that it was probably the ancestral condition of flying pennaraptorans. This discovery of a flight-performance-maintaining center out molting strategy in the Late Jurassic suggests the presence of two sequential molting strategies in the earliest pennaraptorans soon after the presumably non-systematic molting of the flightless pennaraptoran ancestor. This suggests that the evolutionary forces affecting the earliest pennaraptoran fliers included the optimization of molting strategies to benefit flight performance. Understanding why these strategies predate later flight-related innovations like the keeled sternum, pygostyle, and triosseal canal31,32,33,34,35 would be important future priorities and underscores the complexity of flight-related evolutionary changes along the lineage to modern birds.


Archaeopteryx specimen WDC-CSG-100 – known colloquially as the ‘Thermopolis specimen’ – is housed at the Wyoming Dinosaur Center (Thermopolis, Wyoming, USA) where it is on permanent display to the general public and available to qualified researchers for academic study14. WDC-CSG-100 was photographed under white light and LSF. The camera was a Nikon D810 with a Sigma 35-mm lens. A 405 nanometer laser diode was projected through a line lens produced by Laser Line Optics Canada and scanned over the specimen according to the protocol outlined in Kaye et al.15 and extended in Wang et al.36. Color was equalized in the images using Photoshop CS6 to ensure that the fluorescence signal was fully documented and analyzed.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

All the data associated with this paper is available in full in the paper. The specimen WDC-CSG-100 is housed at the Wyoming Dinosaur Center, Thermopolis, Wyoming, USA.


  1. 1.

    Swaddle, J. P. & Witter, M. S. The effects of molt on the flight performance, body mass, and behavior of European starlings (Sturnus vulgaris): an experimental approach. Can. J. Zool. 75, 1135–1146 (1997).

    Article  Google Scholar 

  2. 2.

    Hedenström, A. & Sunada, S. On the aerodynamics of molt gaps in birds. J. Exp. Biol. 202, 67–76 (1999).

    PubMed  Google Scholar 

  3. 3.

    Pyle, P. Staffelmauser and other adaptive strategies for wing molt in larger birds. West. Birds 37, 179–185 (2006).

    Google Scholar 

  4. 4.

    Zuberogoitia, I., Zabala, J. & Martínez, J. E. Moult in birds of prey: a review of current knowledge and future challenges for research. Ardeola 65, 183–207, 125 (2018).

    Article  Google Scholar 

  5. 5.

    Pyle, P. Remigial molt patterns in North American Falconiformes as related to age, sex, breeding status, and lift-history strategies. Condor 107, 823–834 (2005).

    Article  Google Scholar 

  6. 6.

    Hedenström, A. & Sunada, S. On the aerodynamics of moult gaps in birds. J. Exp. Biol. 202, 67–76 (1999).

    PubMed  Google Scholar 

  7. 7.

    Pittman, M. & Xu, X. Pennaraptoran Dinosaurs: Past Progress and New Frontiers 440 (Bulletin of the American Museum of Natural History, 2020).

  8. 8.

    Maryánska, T., Osmólska, H. & Wolsan, M. Avialan status for Oviraptorosauria. Acta Palaeontol. Pol. 47, 97–116 (2002).

    Google Scholar 

  9. 9.

    Turner, A. H., Makovicky, P. J. & Norell, M. A. A review of dromaeosaurid systematics and paravian phylogeny. Bull. Am. Mus. Nat. Hist. 371, 1–206 (2012).

    Article  Google Scholar 

  10. 10.

    Kiat, Y. et al. Sequential moult in a feathered dinosaur and implications for early paravian locomotion and ecology. Curr. Biol. 30, 3633–3638.e2 (2020).

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Pei, R. et al. Potential for powered flight neared by most close avialan relatives but few crossed its thresholds. Curr. Biol. 30, 4033–4046.e8 (2020).

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Wellnhofer, P. Archaeopteryx - The Icon of Evolution. (Verlag Dr. Friedrich Pfeil, 2009).

  13. 13.

    Mayr, G., Pohl, B., Hartman, S. & Peters, D. S. The tenth skeletal specimen of Archaeopteryx. Zool. J. Linn. Soc. 149, 97–116 (2007).

    Article  Google Scholar 

  14. 14.

    Mayr, G., Pohl, B. & Peters, D. S. A well-preserved Archaeopteryx specimen with theropod features. Science 310, 1483–1486 (2005).

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Kaye, T. G. et al. Laser-stimulated fluorescence in paleontology. PLoS ONE 10, e0125923 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Kaye, T. G., Pittman, M., Mayr, G., Schwarz, D. & Xu, X. Detection of lost calamus challenges identity of isolated Archaeopteryx feather. Sci. Rep. 9, 1182 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Foth, C., Tischlinger, H. & Rauhut, O. W. M. New specimen of Archaeopteryx provides insights into the evolution of pennaceous feathers. Nature 511, 79–82 (2014).

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Tischlinger, H. & Unwin, D. UV-untersuchungen des berliner exemplars von Archaeopteryx lithographica H. v. Meyer 1861 und der isolierten Archaeopteryx-Feder. Archaeopteryx 22, 17–50 (2004).

    Google Scholar 

  19. 19.

    Tischlinger, H. Neue informationen zum Berliner exemplar von Archaeopteryx lithographica H.v.Meyer 1861. Archaeopteryx 23, 33–50 (2005).

    Google Scholar 

  20. 20.

    Yu, M. et al. The developmental biology of feather follicles. Int. J. Dev. Biol. 48, 181–191 (2004).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  21. 21.

    Xu, X. et al. A bizarre Jurassic maniraptoran theropod with preserved evidence of membranous wings. Nature 521, 70–73 (2015).

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Wang, M., O’Connor, J. M. K., Xu, X. & Zhou, Z. H. A new Jurassic scansoriopterygid and the loss of membranous wings in theropod dinosaurs. Nature 569, 256–259 (2019).

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Bergmann, U. et al. Archaeopteryx feathers and bone chemistry fully revealed via synchrotron imaging. Proc. Natl Acad. Sci. USA 107, 9060–9065 (2010).

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Göhlich, U. B. & Chiappe, L. M. A new carnivorous dinosaur from the Late Jurassic Solnhofen archipelago. Nature 440, 329–332 (2006).

    Article  PubMed  Google Scholar 

  25. 25.

    Frey, E., Tischlinger, H., Buchy, M. C. & Martill, D. M. Evolution and Palaeobiology of Pterosaurs, Vol. 217 (eds Buffetaut, E. & Mazin, J. M.) 233–266 (Geological Society of London, Special Publications, 2003).

  26. 26.

    Proctor, N. S. & Lynch, P. J. Manual of Ornithology: Avian Structure & Function. 340 (Yale University Press, 1993).

  27. 27.

    Vinther, J. et al. 3D camouflage in an ornithischian dinosaur. Curr. Biol. 26, P2456–2462 (2016).

    Article  Google Scholar 

  28. 28.

    Mayr, G., Pittman, M., Saitta, E., Kaye, T. G. & Vinther, J. Structure and homology of Psittacosaurus tail bristles. Palaeontology 59, 793–802 (2016).

    Article  Google Scholar 

  29. 29.

    O’Connor, J. M. K., Falk, A., Wang, M. & Zheng, X. T. First report of immature feathers in juvenile enantiornithines from the Early Cretaceous Jehol avifauna. Vertebrata PalAsiatica 58, 24–44 (2019).

    Google Scholar 

  30. 30.

    Xu, X. et al. Mosaic evolution in an asymmetrically feathered troodontid dinosaur with transitional features. Nat. Commun. 8, 14972 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Dececchi, T. A., Larrson, H. C. E., Pittman, M. & Habib, M. B. Pennaraptoran Dinosaurs: Past Progress and New Frontiers, Vol. 440 (eds Pittman, M. & Xu, X.) 295–320 (Bulletin of the American Museum of Natural History, 2020).

  32. 32.

    Baier, D. B., Gatesy, S. M. & Jenkins, F. A. A critical ligamentous mechanism in the evolution of avian flight. Nature 445, 307–310 (2007).

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Zheng, X. T. et al. On the absence of sternal elements in Anchiornis (Paraves) and Sapeornis (Aves) and the complex early evolution of the avian sternum. Proc. Natl Acad. Sci. USA 111, 13900–13905 (2014).

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Pittman, M., Gatesy, S. M., Upchurch, P., Goswami, A. & Hutchinson, J. R. Shake a tail feather: the evolution of the theropod tail into a stiff aerodynamic surface. PLoS ONE 8, e63115 (2013).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Gatesy, S. M. New Perspectives on The Origin and Early Evolution of Birds (eds Gauthier, J. & Gall, J. F.) 333–350 (A special publication of the Peabody Museum of Natural History, Yale University, 2001).

  36. 36.

    Wang, X. L. et al. Basal paravian functional anatomy illuminated by high-detail body outline. Nat. Commun. 8, 14576 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

Download references


We thank Levi Shinkle, Wyoming Dinosaur Center, for photography assistance, Gerald Mayr for helpful comments and suggestions, Burkhard Pohl and the Wyoming Dinosaur Center for lab space. This study was supported by the RAE Improvement Fund of the Faculty of Science, The University of Hong Kong (HKU) (to M.P. and T.G.K.), the General Research Fund of the Research Grant Council (17120920) (to M.P. and T.G.K.), and funds from the HKU MOOC course Dinosaur Ecosystems (to M.P.).

Author information




All authors (T.G.K., M.P., and W.R.W.) designed the project. T.G.K., M.P. and W.R.W. collected and analyzed the data. T.G.K. and M.P. wrote the paper. All the authors gave feedback on the paper before submission.

Corresponding authors

Correspondence to Thomas G. Kaye or Michael Pittman.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Kaye, T.G., Pittman, M. & Wahl, W.R. Archaeopteryx feather sheaths reveal sequential center-out flight-related molting strategy. Commun Biol 3, 745 (2020).

Download citation


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing