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An elongating spermatid nearing the climax of elongation in the seminiferous epithelium of Pelamis platurus. The acrosomal complex and apical nucleus is on display in sagittal section (A,E) and with represented cross sections through the letters B,C,D,F,G. All of the major parts of this complex that are found in the typical ophidian spermatozoa are present. Ac, acrosomal complex; Ma, manchette; Av, acrosomal vesicle; black arrowhead and Pe, perforatorium; Sa, subascrosomal space; Ar, acrosomal lucent zone; Sm, Sertoli cell membrane laminae; white arrow and EP, epinuclear lucent zone; Nr, nuclear rostrum; Bp, basal plate; white arrowhead, nuclear lacuna. Bars D 1 mm.  

An elongating spermatid nearing the climax of elongation in the seminiferous epithelium of Pelamis platurus. The acrosomal complex and apical nucleus is on display in sagittal section (A,E) and with represented cross sections through the letters B,C,D,F,G. All of the major parts of this complex that are found in the typical ophidian spermatozoa are present. Ac, acrosomal complex; Ma, manchette; Av, acrosomal vesicle; black arrowhead and Pe, perforatorium; Sa, subascrosomal space; Ar, acrosomal lucent zone; Sm, Sertoli cell membrane laminae; white arrow and EP, epinuclear lucent zone; Nr, nuclear rostrum; Bp, basal plate; white arrowhead, nuclear lacuna. Bars D 1 mm.  

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Little is known about spermatid development during spermiogenesis in snakes, as there is only one complete study in ophidians, which details the spermatid ultrastructure within the viperid, Agkistrodon piscivorus. Thus, the following study will add to our understanding of the ontogenic steps of spermiogenesis in snakes by examining spermatid matura...

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Citations

... The spermatozoa of M. corallinus have three regions: head, midpiece, and tail, which is similar to that described in other reptiles (Oliver et al. 1996). The sperm morphology of elapid snakes has been poorly studied (Oliver et al. 1996;Gribbins et al. 2016) and for Micrurus, sperm morphology has been described only in M. fulvius (Austin 1965). Therefore, this is the first paper describing the sperm morphology of M. corallinus. ...
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... The spermatozoa of M. corallinus have three regions: head, midpiece, and tail, which is similar to that described in other reptiles (Oliver et al. 1996). The sperm morphology of elapid snakes has been poorly studied (Oliver et al. 1996;Gribbins et al. 2016) and for Micrurus, sperm morphology has been described only in M. fulvius (Austin 1965). Therefore, this is the first paper describing the sperm morphology of M. corallinus. ...
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... One of these approaches is the ultrastructural study of the morphological variability of spermatozoa (Oliver et al. 1996;Tavares-Bastos et al. 2002;Tourmente et al. 2006;Rheubert et al. 2010;Gribbins et al. 2016), which can be applied to a reproductive perspective of sperm competition and storage (Vieira et al. 2004;Cunha et al. 2008). The size of the spermatozoa may indicate levels of sperm competition (Tourmente et al. 2009). ...
... Snake ultrastructural spermatozoa studies have produced data on the families Colubridae, Pythonidae (Jamieson & Koehler 1994;Oliver et al. 1996), Viperidae (Al-Dokhi 2004), Typhlopidae (Harding et al. 1995), and Boidae ). However, a few studies were dedicated to describe the spermatozoa of some Elapidae (Oliver et al. 1996;Gribbins et al. 2016) and the neotropical Elapidae remains completely unknown. ...
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... Snake ultrastructural spermatozoa studies have produced data on the families Colubridae, Pythonidae (Jamieson & Koehler 1994;Oliver et al. 1996), Viperidae (Al-Dokhi 2004), Typhlopidae (Harding et al. 1995), and Boidae ). However, a few studies were dedicated to describe the spermatozoa of some Elapidae (Oliver et al. 1996;Gribbins et al. 2016) and the neotropical Elapidae remains completely unknown. ...
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