Literature DB >> 16127704

Development of the uterine shell glands during the preovulatory and early gestation periods in oviparous and viviparous Lacerta vivipara.

Benoit Heulin1, James R Stewart, Yann Surget-Groba, Patricia Bellaud, Florence Jouan, Gérard Lancien, Jean Deunff.   

Abstract

The evolutionary process leading to the emergence of viviparity in Squamata consists of lengthening the period of egg retention in utero coupled with marked reduction in the thickness of the eggshell. We used light microscopy and scanning electron microscopy to study uterine structure during the reproductive cycle of oviparous and viviparous females of the reproductively bimodal Lacerta vivipara. We compared the structure of the uterine shell glands, which secrete components of the eggshell, during preovulatory and early gestation phases of the reproductive cycle and also compared histochemistry of the eggshells. The uterine glands of both reproductive forms undergo considerable growth within a period of a few weeks during folliculogenesis and vitellogenesis preceding ovulation. The majority of the proteinaceous fibers of the shell membrane are secreted early in embryonic development and the uterine glands regress shortly thereafter. This supports previous observations indicating that, in Squamata, secretion of the shell membrane occurs very rapidly after ovulation. The most striking differences between reproductive modes were larger uterine glands at late vitellogenesis in oviparous females, 101 microm compared to 60 microm in viviparous females, and greater thickness of the shell membrane during early gestation in oviparous females (52-73 microm) compared to viviparous females (4-8 microm). Our intraspecific comparison supports the conclusions of previous studies that, prior to ovulation, the uterine glandular layer is less developed in viviparous than in oviparous species, and that this is the main factor accounting for differences in the thickness of the shell membrane of the two reproductive forms of squamates. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16127704     DOI: 10.1002/jmor.10368

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  4 in total

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Authors:  Jonathan W Paul; Joshua O Kemsley; Trent A Butler; Jorge M Tolosa; Michael B Thompson; Roger Smith; Camilla M Whittington
Journal:  J Comp Physiol B       Date:  2019-12-19       Impact factor: 2.200

2.  Facultative oviparity in a viviparous skink ( Saiphos equalis).

Authors:  Melanie K Laird; Michael B Thompson; Camilla M Whittington
Journal:  Biol Lett       Date:  2019-04-26       Impact factor: 3.703

3.  The functional genetic architecture of egg-laying and live-bearing reproduction in common lizards.

Authors:  Hans Recknagel; Madeleine Carruthers; Andrey A Yurchenko; Mohsen Nokhbatolfoghahai; Nicholas A Kamenos; Maureen M Bain; Kathryn R Elmer
Journal:  Nat Ecol Evol       Date:  2021-10-07       Impact factor: 15.460

4.  Understanding the evolution of viviparity using intraspecific variation in reproductive mode and transitional forms of pregnancy.

Authors:  Camilla M Whittington; James U Van Dyke; Stephanie Q T Liang; Scott V Edwards; Richard Shine; Michael B Thompson; Catherine E Grueber
Journal:  Biol Rev Camb Philos Soc       Date:  2022-01-30
  4 in total

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