File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Spermatogenesis of the green-lipped mussel Perna viridis with dual patterns of acrosome and tail development in spermatids

TitleSpermatogenesis of the green-lipped mussel Perna viridis with dual patterns of acrosome and tail development in spermatids
Authors
KeywordsAcrosome formation
Flagellum development
Perna viridis
Spermatogenesis
Issue Date1999
PublisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/10152
Citation
Helgoland Marine Research, 1999, v. 53 n. 1, p. 62-69 How to Cite?
AbstractSpermatogenesis in the mussel Perna viridis was studied by electron microscopy. Results demonstrated that cytological development in spermatogonia and spermatocytes was similar to that previously described in other Mytilidae. Acrosome formation began with the arising of proacrosomal vesicles in spermatogonia. The abundance of proacrosomal vesicles increased in spermatocytes, which were flagellated. However, during spermiogenesis, dual patterns of acrosome development as well as flagellum development could be found among spermatids in a male gonad. The two lines of acrosome formation in spermatids ultimately gave rise to morphologically similar acrosomes. The two lines of flagellum development in spermatids resulted in the formation of sperm cells with either a typically posteriorly directed tail or an anteriorly directed tail. © Springer-Verlag and AWI 1999.
Persistent Identifierhttp://hdl.handle.net/10722/92804
ISSN
2015 Impact Factor: 1.509
2015 SCImago Journal Rankings: 0.750
References

 

DC FieldValueLanguage
dc.contributor.authorReunov, AAen_HK
dc.contributor.authorAu, DWTen_HK
dc.contributor.authorWu, RSSen_HK
dc.date.accessioned2010-09-17T10:57:39Z-
dc.date.available2010-09-17T10:57:39Z-
dc.date.issued1999en_HK
dc.identifier.citationHelgoland Marine Research, 1999, v. 53 n. 1, p. 62-69en_HK
dc.identifier.issn1438-387Xen_HK
dc.identifier.urihttp://hdl.handle.net/10722/92804-
dc.description.abstractSpermatogenesis in the mussel Perna viridis was studied by electron microscopy. Results demonstrated that cytological development in spermatogonia and spermatocytes was similar to that previously described in other Mytilidae. Acrosome formation began with the arising of proacrosomal vesicles in spermatogonia. The abundance of proacrosomal vesicles increased in spermatocytes, which were flagellated. However, during spermiogenesis, dual patterns of acrosome development as well as flagellum development could be found among spermatids in a male gonad. The two lines of acrosome formation in spermatids ultimately gave rise to morphologically similar acrosomes. The two lines of flagellum development in spermatids resulted in the formation of sperm cells with either a typically posteriorly directed tail or an anteriorly directed tail. © Springer-Verlag and AWI 1999.en_HK
dc.languageengen_HK
dc.publisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/10152en_HK
dc.relation.ispartofHelgoland Marine Researchen_HK
dc.subjectAcrosome formationen_HK
dc.subjectFlagellum developmenten_HK
dc.subjectPerna viridisen_HK
dc.subjectSpermatogenesisen_HK
dc.titleSpermatogenesis of the green-lipped mussel Perna viridis with dual patterns of acrosome and tail development in spermatidsen_HK
dc.typeArticleen_HK
dc.identifier.emailWu, RSS: rudolfwu@hku.hken_HK
dc.identifier.authorityWu, RSS=rp01398en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-0002254661en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0002254661&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume53en_HK
dc.identifier.issue1en_HK
dc.identifier.spage62en_HK
dc.identifier.epage69en_HK
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridReunov, AA=55408800400en_HK
dc.identifier.scopusauthoridAu, DWT=7004909228en_HK
dc.identifier.scopusauthoridWu, RSS=7402945079en_HK

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats