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The internal-brooding apparatus in the bryozoan genus Cauloramphus (Cheilostomata : Calloporidae) and its inferred homology to ovicells. / Ostrovsky, Andrew N.; Dick, Matthew H.; Mawatari, Shunsuke F.

в: Zoological Science, Том 24, № 12, 12.2007, стр. 1187-1196.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Author

Ostrovsky, Andrew N. ; Dick, Matthew H. ; Mawatari, Shunsuke F. / The internal-brooding apparatus in the bryozoan genus Cauloramphus (Cheilostomata : Calloporidae) and its inferred homology to ovicells. в: Zoological Science. 2007 ; Том 24, № 12. стр. 1187-1196.

BibTeX

@article{a0a3c1f3abbe4caebf59b11074e68823,
title = "The internal-brooding apparatus in the bryozoan genus Cauloramphus (Cheilostomata: Calloporidae) and its inferred homology to ovicells",
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.",
keywords = "Bryozoa, Cauloramphus, Evolution, Homology, Internal brooding, Ovicell",
author = "Ostrovsky, {Andrew N.} and Dick, {Matthew H.} and Mawatari, {Shunsuke F.}",
year = "2007",
month = dec,
doi = "DOI: 10.2108/zsj.24.1187",
language = "English",
volume = "24",
pages = "1187--1196",
journal = "Zoological Science",
issn = "0289-0003",
publisher = "Zoological Society of Japan",
number = "12",

}

RIS

TY - JOUR

T1 - The internal-brooding apparatus in the bryozoan genus Cauloramphus (Cheilostomata

T2 - Calloporidae) and its inferred homology to ovicells

AU - Ostrovsky, Andrew N.

AU - Dick, Matthew H.

AU - Mawatari, Shunsuke F.

PY - 2007/12

Y1 - 2007/12

N2 - 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.

AB - 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.

KW - Bryozoa

KW - Cauloramphus

KW - Evolution

KW - Homology

KW - Internal brooding

KW - Ovicell

UR - http://www.scopus.com/inward/record.url?scp=39149139036&partnerID=8YFLogxK

U2 - DOI: 10.2108/zsj.24.1187

DO - DOI: 10.2108/zsj.24.1187

M3 - Article

C2 - 18271635

VL - 24

SP - 1187

EP - 1196

JO - Zoological Science

JF - Zoological Science

SN - 0289-0003

IS - 12

ER -

ID: 5055292