scholarly journals Egg retention and intrauterine embryonic development in Sceloporus aeneus (Reptilia: Phrynosomatidae): implications for the evolution of viviparity

2012 ◽  
Vol 83 (3) ◽  
Author(s):  
Rodolfo García-Collazo ◽  
Maricela Villagrán-Santa Cruz ◽  
Eduardo Morales-Guillaumin ◽  
Rubi Nelsi Meza-Lázaro ◽  
Fausto R. Méndez-de la Cruz
2017 ◽  
Vol 38 (4) ◽  
pp. 557-561 ◽  
Author(s):  
Thomas Foucart ◽  
Benoit Heulin ◽  
Olivier Lourdais

We examined the possible interaction between reproductive effort and embryonic stages at oviposition in oviparous form of the lizard Zootoca vivipara. Our results reveal that the percentage of total embryonic development time (%TEDT) reached at oviposition is negatively correlated to clutch size (adjusted to maternal body size). We found no influence of reproductive burden of female (relative clutch mass, RCM) on %TEDT. The significant effect of fecundity supports the hypothesis that a resource limitation such as oxygen may exist for developing embryos in oviducts. The absence of RCM effect suggests that the available space (abdominal burdening of the mother) does not limit the embryonic stages at oviposition.


2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


2014 ◽  
Vol 47 (06) ◽  
Author(s):  
N Bergemann ◽  
K Boyle ◽  
WE Paulus

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