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Couzens, A. M. C.

Publications and source records attributed to Couzens, A. M. C..

2 recordsLinked to original sources

Postnatal Development of the Gray Short Tailed Opossum (Monodelphis domestica): Implications for Metatherian Decline at the K/Pg Boundary

Marsupials give birth to extremely altricial offspring which must be reared externally for an extended period, often in a pouch. Despite often being considered a defining feature of marsupials, around a third of living species lack a pouch. Here, we describe the postnatal development of the gray short-tailed opossum, Monodelphis domestica, a small pouchless South American didelphid and consider its implications for life history evolution within Metatheria. We find that at birth, ossification and chondrogenesis in neonatal M. domestica is more extensive than in basal pouched Australidelphian marsupials like the dunnart. Key precocial milestones such as tarsal ossification, eye opening, growth of body fur, and chewing tooth eruption occur earlier and more rapidly. Principal component analysis of life history and reproductive traits reveals a pronounced r- to K-selected gradient across living marsupial species. Stochastic character-mapping based ancestral state reconstruction suggests that absence of the pouch, and by inference possession of an r-selected life history strategy characterised by large litters, short attachment phases, and accelerated weaning was likely ancestral amongst crown-group marsupials. The more K-selected reproductive strategy of pouched marsupials wherein there is a prolonged postnatal development window, and relative few young are produced, likely evolved during the early Cenozoic, and separately amongst australidelphian and ameridelphian marsupials. Rather than making early marsupials more sensitive to environmental disturbances, we hypothesis that their possession of an r-selected life history strategy may have been a key factor in their persistence through the K-Pg extinction.

developmental biology↗

Getting a head start: Craniofacial heterochrony in marsupials involves dynamic changes to molecular and cellular mechanisms underlying neural crest development

The neural crest is a vertebrate innovation central to craniofacial development and evolution. While the gene regulatory networks guiding neural crest development are well characterized, the mechanisms generating species-specific craniofacial diversity remain poorly understood. Marsupials provide a unique model for studying neural crest plasticity, having evolved accelerated patterns of craniofacial development during embryogenesis. This adaptation arises in response to marsupials being born altricial after a short gestation yet require well-developed mouthparts to attach to a teat and continue development in the pouch. However, how marsupials achieve this heterochronic shift in neural crest development is largely unknown. In this study, we investigate the cellular and molecular mechanisms underlying their distinct heterochrony, revealing that marsupials produce dense pre-migratory aggregates of neural crest cells which undergo collective migration as epithelial-like sheets, potentially facilitating rapid establishment of the facial prominences. These cellular behaviours are unique amongst amniotes but resemble patterns in anamniotes which similarly exhibit accelerated craniofacial development to support early feeding. Marsupials appear to have evolved a similar mechanism of neural crest migration to facilitate their developmental heterochrony. These findings suggest that vertebrate neural crest migration may be shaped by the pace of craniofacial development during embryogenesis rather than phylogeny, providing new perspectives on neural crest plasticity and the developmental mechanisms driving craniofacial diversity across vertebrates.

developmental biology↗