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The Internal-Brooding Apparatus in the Bryozoan Genus Cauloramphus (Cheilostomata: Calloporidae) and Its Inferred Homology to Ovicells

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Title: The Internal-Brooding Apparatus in the Bryozoan Genus Cauloramphus (Cheilostomata: Calloporidae) and Its Inferred Homology to Ovicells
Authors: Ostrovsky, Andrew N. Browse this author
Dick, Matthew H. Browse this author →KAKEN DB
Mawatari, Shunsuke F. Browse this author →KAKEN DB
Keywords: Bryozoa
Cauloramphus
ovicell
internal brooding
evolution
homology
Issue Date: Dec-2007
Publisher: Zoological Society of Japan
Journal Title: Zoological Science
Volume: 24
Issue: 12
Start Page: 1187
End Page: 1196
Publisher DOI: 10.2108/zsj.24.1187
Abstract: We studied by SEM the external morphology of the ooecium in eight bryozoans of the genus Cauloramphus Norman, 1903 (Cheilostomata, Calloporidae): C. spinifer, C. variegatus, C. magnus, C. multiavicularia, C. tortilis, C. cryptoarmatus, C. niger, and C. multispinosus, and by sectioning and light microscopy the anatomy of the brooding apparatus of C. spinifer, C. cryptoarmatus, and C. niger. These species all have a brood sac, formed by invagination of the non-calcified distal body wall of the maternal zooid, located in the distal half of the maternal (egg-producing) autozooid, and a vestigial, maternally budded kenozooidal ooecium. The brood sac comprises a main chamber and a long passage (neck) opening externally independently of the introvert. The non-calcified portion of the maternal distal wall between the neck and tip of the zooidal operculum is involved in closing and opening the brood sac, and contains both musculature and a reduced sclerite that suggest homology with the ooecial vesicle of a hyperstomial ovicell. We interpret the brooding apparatus in Cauloramphus as a highly modified form of cheilostome hyperstomial ovicell, as both types share 1) a brood chamber bounded by 2) the ooecium and 3) a component of the distal wall of the maternal zooid. We discuss Cauloramphus as a hypothetical penultimate stage in ovicell reduction in calloporid bryozoans. We suggest that the internal-brooding genus Gontarella, of uncertain taxonomic affinities, is actually a calloporid and represents the ultimate stage in which no trace of the ooecium remains. Internal brooding apparently evolved several times independently within the Calloporidae.
Type: article
URI: http://hdl.handle.net/2115/56381
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: Matthew Hill Dick

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