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Background <p>Within the symbiont-hosting Siboglinidae (Annelida), <i>Osedax</i> stands out as the sole genus capable of degrading bones and displaying pronounced sexual dimorphism (except <i>O. priapus</i>). While macroscopic, gutless females feed on whale falls with their symbiont-housing “roots”, males are microscopic and non-feeding. Yet, embryos and larvae look identical, and sex is suggested to be environmentally determined, i.e., larvae metamorphose into females on bare bone or into males when finding an adult female.</p> Results <p>However, we here describe a transient gut present in half of the late larvae and in juvenile females of <i>O. japonicus</i>. We confirm the gut-carrying larvae as being females from sex-specific in situ gene expression. Moreover, morphological evidence coupled with differential gene expression indicate that the ‘non-feeding’ transient gut may pattern the vascular system and/or act as a gas-exchange surface in juvenile females, before their branchial appendages develop.</p> Conclusions <p>The transient gut of <i>O. japonicus</i> females reveals a genetic sex determination. Proposedly homologous across siboglinids, this vestigial gut is suggested to function in organ patterning and/or for gas-exchange during development of the gutless adult.</p>

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Predetermined sex revealed by a female transient gut in non-feeding larvae of Osedax (Siboglinidae, Annelida)

  • 期刊论文

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  • 发表日期：

    2025年8月26日

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  • Alice Rouan,
  • Norio Miyamoto,
  • Katrine Worsaae

摘要

Background

Within the symbiont-hosting Siboglinidae (Annelida), Osedax stands out as the sole genus capable of degrading bones and displaying pronounced sexual dimorphism (except O. priapus). While macroscopic, gutless females feed on whale falls with their symbiont-housing “roots”, males are microscopic and non-feeding. Yet, embryos and larvae look identical, and sex is suggested to be environmentally determined, i.e., larvae metamorphose into females on bare bone or into males when finding an adult female.

Results

However, we here describe a transient gut present in half of the late larvae and in juvenile females of O. japonicus. We confirm the gut-carrying larvae as being females from sex-specific in situ gene expression. Moreover, morphological evidence coupled with differential gene expression indicate that the ‘non-feeding’ transient gut may pattern the vascular system and/or act as a gas-exchange surface in juvenile females, before their branchial appendages develop.

Conclusions

The transient gut of O. japonicus females reveals a genetic sex determination. Proposedly homologous across siboglinids, this vestigial gut is suggested to function in organ patterning and/or for gas-exchange during development of the gutless adult.