scholarly journals Associations Between Egg Capsule Morphology and Predation Among Populations of the Marine Gastropod, Nucella emarginata

1990 ◽  
Vol 179 (3) ◽  
pp. 312-325 ◽  
Author(s):  
T. A. Rawlings

1984 ◽  
Vol 167 (2) ◽  
pp. 378-389 ◽  
Author(s):  
CHARLES H. SULLIVAN ◽  
TIMOTHY K. MAUGEL


2004 ◽  
Vol 273 ◽  
pp. 163-172 ◽  
Author(s):  
C Martel ◽  
F Viard ◽  
D Bourguet ◽  
P Garcia-Meunier


2020 ◽  
Vol 39 (2) ◽  
pp. 419
Author(s):  
Yi Yang ◽  
Lu Qi ◽  
Lingfeng Kong ◽  
Qi Li
Keyword(s):  


Zootaxa ◽  
2020 ◽  
Vol 4732 (1) ◽  
pp. 196-200
Author(s):  
CHANG-MOON JANG ◽  
YANG˗SEOP BAE

Parapachymorpha is one of eight genera within the tribe Medaurini of subfamily Clitumninae (Phasmatidae). It was established by Brunner von Wattenwyl (1893), with the type species Parapachymorpha nigra by subsequent designation of Kirby (1904), from Myanmar. Species of this genus are widely distributed in oriental tropics (Laos, China, Thailand, Myanmar, Vietnam and Cambodia), with only 11 known species in the world (Brock et al. 2018, Ho 2017). Species of the genus Parapachymorpha can be recognized by following characters (Brunner von Wattenwyl 1893;1907, Henmemann & Conle 2008, Ho 2017): 1) body robust in female and slender in male with long leg in relation to the length; 2) body surface of female granulose or spinose; 3) mesonotum of female more and less expanded posteriorly; 4) abdominal tergites lacking expanded prostero–lateral angles in both sexes; 5) laminal supraanalis undeveloped in female; 6) semi–tergite of male irregularly rectangular, with an additional finger­–like ventro–apical appendix on the lower margin and reduced or absent; 7) egg capsule oval to oblong and covered with a raised net–like structure in lateral view; 8) micropylar plate oval; 9) operculum concave or convex. In the present study, we describe additional species, Parapachymorpha minuta sp. nov. from Laos, with photographs of both sexes of adults and egg. 



2018 ◽  
Vol 4 (1) ◽  
pp. 37-38
Author(s):  
Hana Kim ◽  
Cheol Yu ◽  
Hyung June Kim ◽  
Yun-Hwan Jung


1970 ◽  
Vol 119 (1) ◽  
pp. 39-47 ◽  
Author(s):  
Michiko Nishida-Fukuda ◽  
Fujio Egami

1. A multienzyme system capable of degrading keratosulphates to yield galactose, N-acetylglucosamine and sulphate was found in the liver extract of a marine gastropod, Charonia lampas. 2. During the degradation, neither oligosaccharides nor sulphated sugars were produced. 3. It is suggested that the degradation could be attributed to the concerted action of β-galactosidase, β-N-acetylglucosaminidase and a sulphatase (sulphohydrolase), tentatively designated keratosulphatase. 4. Two forms of keratosulphatase (I and II) were separated by DEAE-Sephadex column chromatography. Both forms could release all the sulphate from keratosulphates and neither appeared to be identical with glycosulphatase or chondrosulphatase, both of which are also present in Charonia lampas. 5. β-Galactosidase and β-N-acetylglucosaminidase could degrade keratopolysulphate to a greater extent in the presence of keratosulphatase than in its absence. 6. It is suggested that keratosulphate was first desulphated by the action of keratosulphatase, and the desulphated polymer was then degraded to galactose and N-acetylglucosamine by the action of β-galactosidase and β-N-acetylglucosaminidase. 7. β-Galactosidase alone released a small amount of galactose from shark cartilage keratopolysulphate, but β-N-acetylglucosaminidase alone did not release N-acetylglucosamine. This indicates that unsulphated galactose residues occupy all the non-reducing terminal positions in keratopolysulphate chains.



2014 ◽  
Vol 31 (12) ◽  
pp. 810 ◽  
Author(s):  
Nobuko Katagiri ◽  
Yasuo Katagiri ◽  
Masaaki Wada ◽  
Daisuke Okano ◽  
Yasuhide Shigematsu ◽  
...  


2002 ◽  
Vol 19 (11) ◽  
pp. 1231-1240 ◽  
Author(s):  
Nobuko Katagiri ◽  
Tatsuo Suzuki ◽  
Yuichi Shimatani ◽  
Yasuo Katagiri


Parasitology ◽  
1964 ◽  
Vol 54 (2) ◽  
pp. 295-312 ◽  
Author(s):  
Elon E. Byrd ◽  
William P. Maples

The naturally oviposited egg of Dasymetra conferta is fully embryonated and it hatches only after it is ingested by the snail host, Physa spp.Hatching appears to be in response to some stimulus supplied by the living snail. The stimulus causes the larva to exercise a characteristic series of body movements and to liberate a granular sustance (hatching enzyme) from the larger pair of its cephalic glands. This enzyme reacts with the vitelline fluid to create pressure within the egg capsule, and with the cementum of the operculum, so that it may be lifted away. The larva's escape from the shell, therefore, is due to a combination of pressure and body movements.The hatched larva has a membranous body wall, supporting six epidermal plates, an apical papilla, two penetration glands and a central matrix (the presumptive brood mass).It lives for about an hour within the snail and during this time there is a reorganization of the central matrix which terminates in the formation of an 8-nucleated syncytial brood mass.The miracidial ‘case’, consisting of the body wall and the epidermal plates, ultimately ruptures to liberate the brood mass. Once the brood mass is free it penetrates through the gut wall in an incredibly short time.



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