image: Figure 1. Fossilized nits of chewing lice, tightly affixed to feathers of an enantiornithine bird, entombed in mid-Cretaceous amber from northern Myanmar. (a) Isolated barbs and regularly arranged louse nits attached to two barbs of the same type. (b) Enlargement of six louse nits (indicated with black arrows). (c) Enlargement of five louse nits (indicated with white arrows). (d) and (e), Enlargement of louse nits. (f) Details of a nit, showing the placement, attachment, and details of the chorion. (g) Enlargement of two louse nits, showing the attachments to ramus. (h) Ecological reconstruction of Cretaceous chewing lice of an enantiornithine bird. (a–c) Under normal reflected light. (d–f) Under confocal laser scanning microscopy. (g) Under X-ray micro-computed tomography. Abbreviations: ch, chorion; eg, egg; ra, ramus.
Credit: ©Science China Press
The evolution of ectoparasitism in insects has occurred independently multiple times, with parasitic species that feed on blood, feathers, or other external tissues exerting profound impacts on the adaptive evolution of their hosts. However, fossil evidence directly revealing such parasitic behaviors is exceptionally rare, especially for Mesozoic parasites that specifically fed on feathers.
Recently, a team led by Prof. Diying Huang from the Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, published a study in National Science Review. The study reports the discovery of fossilized chewing lice eggs preserved in mid-Cretaceous Burmese amber, marking the first direct evidence of ectoparasitic lice feeding on feathers of stem-group birds during the Mesozoic. This discovery offers valuable insights into the origins of lice and their early coevolution with vertebrate hosts.
The research team identified a rare and unique amber specimen containing fossilized chewing lice eggs affixed to small feather fragments. Two slender feather barbs are preserved within the amber, with each barb hosting a row of regularly spaced, elongated eggs attached along its shaft. Measuring approximately 512 micrometers in length and spaced 526 to 748 micrometers apart, the eggs adhered to the feather shaft using a cement-like substance. Unlike modern bird lice eggs, which exhibit certain structural similarities, the fossilized eggs display distinct differences in attachment area and arrangement.
Microscopic examination and morphological analysis of the feathers suggest that they belonged to enantiornithines, an extinct group of basal birds that were highly diverse and abundant during the Mesozoic. The discovery of these lice eggs in association with enantiornithine feathers strongly supports the hypothesis that Mesozoic bird lice were parasitic on early feathered vertebrates.
Lice are among the most common ectoparasites in modern animals, predominantly infesting birds and mammals. Studies suggest that modern lice originated at least 99 million years ago during the Mesozoic and exhibit distinct ecological and morphological differences from their free-living relatives in the Liposcelididae family. Earlier research had uncovered fossilized adult lice in Burmese amber, but the newly discovered lice eggs provide even more direct evidence of early parasitic behavior. This discovery bolsters the hypothesis that lice established parasitic relationships with basal birds early in their evolutionary history.
The divergence of modern bird lice from mammalian lice is believed to have resulted from an ancient host-switching event. Fossil evidence supports this idea, including the discovery of lice eggs associated with mammalian hair in Eocene Baltic amber. The mid-Cretaceous bird lice eggs described in this study suggest that early enantiornithines may have been among the first hosts to support the evolution of lice from free-living ancestors to obligate parasites.
This discovery represents the earliest fossil record of lice eggs and provides a new perspective on the origins and evolution of ectoparasitic lice. The findings indicate that early feather lice were already capable of completing their life cycle on enantiornithine feathers, exhibiting ecological specialization similar to that of modern lice. This discovery not only fills a significant gap in the fossil record of lice but also sheds light on the evolution of parasitism and the intricate ecological interactions between insects and vertebrates during the Mesozoic. Continued exploration of amber fossils may reveal further details about these ancient relationships, offering key insights into the formation and maintenance of modern ecosystems.
###
See the article:
Cretaceous chewing-louse eggs on enantiornithine birds
https://doi.org/10.1093/nsr/nwae479
Journal
National Science Review