1993
DOI: 10.1071/zo9930537
|View full text |Cite
|
Sign up to set email alerts
|

The Ultrastructure of the Spermatozoon of Dromidiopsis-Edwardsi Rathbun, 1919 (Crustacea, Brachyura, Dromiidae) - Confirmation of a Dromiid Sperm Type

Abstract: The dromiid spermatozoon, as exemplified by Dromidiopsis edwardsi, Stimdromia (=Petalomera) lateralis and Dromidia antillensis, accords with that of the Homolidae and differs markedly from spermatozoa of other crabs (the raninid-heterotreme-thoracotreme assemblage) in the discoidal form of the acrosome and the capitate form of the perforatorium. Dromiids differ from homolids in the greater depression of the acrosome and the form of the head of the perforatorium, thus exhibiting a distinctive dromiid sperm type… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
10
0

Year Published

1993
1993
2018
2018

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(10 citation statements)
references
References 28 publications
0
10
0
Order By: Relevance
“…The mean ratios of length to width of the acrosome of 0.54-0.63 overlap with mean ratios in raninoids which range from 0.53 in Lyreidus brevipons Sakai, 1937, to 0.76 in Ranina ranina (Lime, 1758) (see Jamieson, 1989) and 0.68-0.72 in Raninoides sp. and is greater than the 0.26 and 0.34 in the dromiids Petalomera lateralis Gray, 183 1, now Stirndromia lateralis (see McLay , 1993;Jamieson, 1990) and Dromidiopsis edwarhi Rathbun, 1919 (Jamieson et al, 1993) or 0.35 in the dynomenid Paradynomene tuberculata Sakai, 1963(Jamieson et al, 1993a. Other species with mean lengthwidth ratios lying within the lower limit for raninoids are the homolids Homola sp.…”
Section: Discussionmentioning
confidence: 93%
“…The mean ratios of length to width of the acrosome of 0.54-0.63 overlap with mean ratios in raninoids which range from 0.53 in Lyreidus brevipons Sakai, 1937, to 0.76 in Ranina ranina (Lime, 1758) (see Jamieson, 1989) and 0.68-0.72 in Raninoides sp. and is greater than the 0.26 and 0.34 in the dromiids Petalomera lateralis Gray, 183 1, now Stirndromia lateralis (see McLay , 1993;Jamieson, 1990) and Dromidiopsis edwarhi Rathbun, 1919 (Jamieson et al, 1993) or 0.35 in the dynomenid Paradynomene tuberculata Sakai, 1963(Jamieson et al, 1993a. Other species with mean lengthwidth ratios lying within the lower limit for raninoids are the homolids Homola sp.…”
Section: Discussionmentioning
confidence: 93%
“…In the most recent investigations dealing with the spermatophore morphometry of hermit crabs (Jamieson & Tudge, 1990;Tudge & Jamieson, 1991Jamieson et al, 1993Jamieson et al, , 1997Tudge, 1996Tudge, , 1997aTudge, , b, 1999Tudge et al, 1998aTudge et al, , 1999Tudge et al, , 2001, usually one or two crabs for each species were used and 4-12 spermatophores were measured (sampling defined as representative by Tudge et al, 1998a), but Scelzo et al (2004) measured larger samples. Such small numbers do not permit the use of multivariate analysis.…”
Section: Sample Collection and Preparationmentioning
confidence: 99%
“…It is unknown in other crabs, being distinct from the apical button of thoracotreme sperm. Homology with the subopercular zone of other brachyurans is uncertain (Jamieson et al, 1993). Apical perforation of the operculum occurs also in dromiids and homolids and also in raninoids, cyclodorippoids and * Now Stimdromia lateralis (Gray, 1831) lower (e.g.…”
Section: Nucleusmentioning
confidence: 99%
“…The operculum is interrupted, centrally, by a hiatus; (2) moderately dense material protrudes from below the operculum through the perforation as an apically rounded cone. The layer of which the protuberance is an extension is here termed the subopercular zone, though homology with a zone of the same name in other brachyurans is uncertain (Jamieson et al, 1993). The subopercular zone directly overhes the capitate expansion of the perforatorium.…”
Section: Acrosomementioning
confidence: 99%
See 1 more Smart Citation