The anatomical innovation of sound-producing organs, which gives rise to a wide variety of sound signals, is one of the most fundamental factors leading to the explosive speciation of modern birds. Despite being a key clue to resolving the homology of sound-controlling muscles among birds, only few studies have explored the embryonic development of syringeal muscles. Using serial histological sections and immunohistochemistry, we described the three-dimensional anatomy and development of the cartilage, muscle, and innervation pattern of the tracheobronchi in three avian species: domestic fowls, cockatiels, and zebra finches. Crucially, the muscle primordia of the syringeal and tracheobronchial muscles develop from the caudal end of the lateral tracheal muscle in cockatiels and zebra finches. Furthermore, the tracheobronchial and syringeal muscle primordia of the zebra finches are subsequently split during embryonic development. Based on our findings on the identity of muscle primordia development and innervation pattern of the hypoglossal nerve between the cockatiels and zebra finches, we suggest that the muscle component traditionally documented as the superficial syringeal muscle in parrots is homologous to the tracheobronchial and ventral syringeal muscles of the zebra finches. These facts not only orchestrate the terminological discrepancies among previous studies, but also suggest that the syringeal muscles were acquired by the anatomical innovation of the lateral tracheal muscles in the common ancestor of the parrots and passerines, and further compartmentalized in the passerines, perhaps leading to a wide song repertoire for acoustic communication.

Download full-text PDF

Source
http://dx.doi.org/10.1111/joa.14189DOI Listing

Publication Analysis

Top Keywords

zebra finches
20
syringeal muscles
12
cockatiels zebra
12
muscle primordia
12
muscles birds
8
anatomical innovation
8
embryonic development
8
innervation pattern
8
lateral tracheal
8
syringeal muscle
8

Similar Publications

Birds are inherently social creatures that rely on pairing to enhance their well-being. Since many bird species lack obvious physical differences between females and males, sex identification is essential for ensuring their welfare. Additionally, early determination of the sexes of birds is crucial for their breeders, especially considering that most companion birds do not display clear sexual characteristics.

View Article and Find Full Text PDF

The amniote pallium, a vital component of the forebrain, exhibits considerable evolutionary divergence across species and mediates diverse functions, including sensory processing, memory formation, and learning. However, the relationships among pallial subregions in different species remain poorly characterized, particularly regarding the identification of homologous neurons and their transcriptional signatures. In this study, we utilized single-nucleus RNA sequencing to examine over 130 000 nuclei from the macaque ( ) neocortex, complemented by datasets from humans ( ), mice ( ), zebra finches ( ), turtles ( ), and lizards ( s), enabling comprehensive cross-species comparison.

View Article and Find Full Text PDF

Delta-opioid receptors (δ-ORs) are known to be involved in associative learning and modulating motivational states. We wanted to study if they were also involved in naturally-occurring reinforcement learning behaviors such as vocal learning, using the zebra finch model system. Zebra finches learn to vocalize early in development and song learning in males is affected by factors such as the social environment and internal reward, both of which are modulated by endogenous opioids.

View Article and Find Full Text PDF

The accurate and reliable performance of learned vocalizations (e.g., speech and birdsong) modulates the efficacy of communication in humans and songbirds.

View Article and Find Full Text PDF

The anatomical innovation of sound-producing organs, which gives rise to a wide variety of sound signals, is one of the most fundamental factors leading to the explosive speciation of modern birds. Despite being a key clue to resolving the homology of sound-controlling muscles among birds, only few studies have explored the embryonic development of syringeal muscles. Using serial histological sections and immunohistochemistry, we described the three-dimensional anatomy and development of the cartilage, muscle, and innervation pattern of the tracheobronchi in three avian species: domestic fowls, cockatiels, and zebra finches.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!