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Salamanders in the family Plethodontidae exhibit a unique tail-straddle walk during courtship that can include the use of sexually dimorphic mental and caudal courtship glands. This study presents novel histological and fine structure data on mental glands and caudal courtship glands in Plethodon mississippi, Desmognathus conanti and Eurycea quadridigitata using both light microscopy and scanning electron microscopy. This study represents the first use of scanning electron microscopy to observe these glands. Both mental and caudal courtship glands were observed to vary seasonally in gland diameter and histology according to the breeding season of each species. Morphological variation was observed across the three species studied in both clustering and relative size of the glands compared to neighbouring mucous and granular glands. Hypertrophied mental glands are larger than mucous or granular glands in all species, but relationships among caudal courtship glands and other skin glands vary among species. In E. quadridigitata, active caudal courtship glands are larger than mucous and granular glands, but in D. conanti, caudal courtship glands are similar in size to granular glands and larger than mucous glands. In P. mississippi, caudal courtship glands are scattered among significantly larger granular glands and are similar in size to mucous glands. [ABSTRACT FROM AUTHOR]

Mental glands are sexually dimorphic glands found in the skin of the submandibular region in males of many species in the salamander family Plethodontidae. These glands have been demonstrated to secrete pheromones that increase female receptivity to courtship and mating. A number of studies exist on the morphology of mental glands at the light microscopy level, but ultrastructural studies on the glands exist for only two species, Eurycea quadridigitata and Hydromantes italicus. In this study, ultrastructure of the mental gland is described from seasonal samples of the eastern North American plethodontid Plethodon cinereus. The mental glands are most hypertrophied in males examined in mating condition (i.e. sperm in their Wolffian ducts) in October and April. In these specimens, 6- to 8-μm electron-dense secretory vacuoles are found in the apical cytoplasm (October) or throughout the entire epithelial cells (April). Mental glands from June and August contain only condensing vacuoles, and the cytoplasm is otherwise packed with stacks of rough endoplasmic reticulum. The ultrastructure of the mental gland of P. cinereus agrees with earlier descriptions for E. quadridigitata and H. italicus. Two other sexually dimorphic skin glands, the caudal courtship gland and the cloacal vent gland, were previously examined from males in this sample of P. cinereus. Although all three glands show similarities in histology and histochemistry at the light microscopy level, they are dissimilar in ultrastructure. Whereas the secretory vacuoles of mental glands are uniformly electron dense, those of caudal courtship glands are smaller (1.2-1.5 μm), oblong and biphasic, and vent glands have spherical biphasic secretory vacuoles (1.8-2.1 μm). This indicates a difference in secretory product and function for the three glands and needs further investigation. Whether other plethodontids show similar variation among sexually dimorphic glands is another topic for future research. [ABSTRACT FROM AUTHOR]

The skin glands and cloacal morphology of the Korean crevice salamander, Karsenia koreana, were similar to those of other plethodontids. The skin contained mucous, granular, and modified granular glands in varying frequencies and sizes. Males had sexually dimorphic glands in the skin of the chin (mental glands) and the dorsal tail base (caudal courtship glands). On the ventral surface of the tail base, modified granular glands were sexually dimorphic in size, with male glands larger than those in females. The cloacal glands in males, as in other plethodontids, consisted of four eosinophilic gland clusters (dorsal pelvic glands, lateral pelvic glands, caudal pelvic glands, and vent glands) and three basophilic glands (anterior ventral glands, posterior ventral glands, and Kingsbury's glands). In females, the only cloacal gland was the spermatheca, which, as in other plethodontids, was a compound tubulo-alveolar gland in the roof of the cloaca. [ABSTRACT FROM AUTHOR]

Studies on reptilian sperm morphology have shown that variation exists at various taxonomic levels but studies on the ontogeny of variation are rare. Sperm development follows a generalized bauplan that includes acrosome development, nuclear condensation and elongation, and flagellar development. However, minute differences can be observed such as the presence/absence of manchette microtubules, structural organization during nuclear condensation, and presence/absence of a nuclear lacuna. The purpose of this investigation was to examine sperm development within the Sceloporus genus. The process begins with the development of an acrosomal complex from Golgi vesicles followed by nuclear condensation and elongation, which results in the presence of a nuclear lacuna. As the acrosomal complex differentiates, flagellar development commences with elongation of the distal centriole. Spermatid development culminates in a mature spermatid with a highly differentiated acrosomal complex, a condensed nucleus with a nuclear lacuna, and a differentiated flagellum. Although the overall developmental pattern is consistent with other squamate species, minute differences are observed, even within the same genus. For example there is variation in the presence/absence of an endoplasmic reticulum complex during acrosome development, presence/absence of a nuclear lacuna, and presence/absence of manchette microtubules within the three species of Sceloporus studied to date. Future studies concerning sperm morphology in closely related species will aid in our understanding of variation in sperm development and may prove to be useful in testing phylogenetic and evolutionary hypotheses. [ABSTRACT FROM AUTHOR]

The article focuses on herpetological research by herpetologists such as Raymond Ditmars and Lawrence Klauber who have influenced undergraduate for research. Topics discussed include elements of maintaining a research program at schools for high-quality teaching such as long-standing research program and emphasis on graduate degrees and suggestions by the author for betterment of the research such as research grant to students.

This paper represents the first ultrastructural descriptions of the cloacal glands of a male salamander. All male salamanders in the suborder Salamandroidea possess these glands, which are required for internal fertilization. These glands are responsible for producing spermatophores and, in some species, certain glands produce female-attracting pheromones. Both scanning and transmission electron microscopy provided higher resolution and magnification of the cytology of cloacal glands than possible in previous studies limited to light microscopy. The glands are hypertrophied in October and April samples, and much reduced in size and secretory activity in June and August samples. Each of the cloacal glands, when active, has secretory vacuoles that are unique in appearance and that secrete carbohydrates and/or proteins. Kingsbury's glands are modified mucous glands that have secretory vacuoles filled with a flocculent substance. Active pelvic glands have uniform electron-lucent secretory vacuoles that fill the cytoplasm and narrow the lumen. Ventral glands have squamous epithelium with moderately dense vacuoles scattered around the apical border, and a granular secretion that fills die wide lumen. In die breeding season, vent glands have biphasic secretory vacuoles characteristic of glycoproteins. All glands release their products by a merocrine process, and all have myoepidielial sheaths, which are best developed in ventral glands. Future research should focus on differences in cytology among die pheromone producing glands and comparisons with the ventral glands in salamander clades that do not produce spermatophores (e.g., Hynobiidae and Cryptobranchidae). [ABSTRACT FROM AUTHOR]

The histology, histochemistry, and ultrastructure of the adhesive breeding glands of male Gastrophryne carolinensis are described. Adhesive glands are mutlicellular exocrine glands in the dermis of the sternum and forearm that cause the male to adhere to the female during amplexus. The epithelial cells have distinct plasma membranes, and the product consists of electron-dense secretory granules that fill the cytoplasm and are released intact by an apocrine process. We support one previous study and contradict another report by finding that adhesive glands react positively for neutral carbohydrates and negatively for glycosaminoglycans and proteins. The ultrastructural results, the first on these organs, confirm that adhesive glands are derived from mucous glands and not serous glands. [ABSTRACT FROM AUTHOR]

The spermatheca of Plethodon cinereus is a compound tubular gland that stores sperm from mating in early spring (March–April) to oviposition in summer (June–July). The seasonal variation of sperm storage in this species has previously been studied by light and transmission electron microscopy. In this paper, sperm aggregations, interaction of sperm with the spermathecal epithelium, and spermathecal secretions are studied using scanning electron microscopy. Within spermathecal tubules, relatively small groups of sperm are aligned along their entire lengths in parallel arrays. This pattern is similar to other plethdontids with complex spermathecae. Lumina of spermathecal tubules are filled with secretory material in April prior to the arrival of sperm, and after sperm appear, a coating of secretory material persists on the apices of the spermathecal epithelium. Sperm peripheral to the central luminal mass can become embedded in the secretory matrix or pushed deeper into the spermathecal epithelium. The spermathecal secretions may serve to attract and prolong the viability of sperm, but sperm that become enmeshed in the secretions or epithelium are phagocytized. Sperm and spermathecal secretions are largely absent after ovulation and in summer months, and new secretory vacuoles are formed in fall, although mating does not occur until spring. [ABSTRACT FROM AUTHOR]

Female salamanders in the suborder Salamandroidea store sperm in cloacal glands called spermathecae. Scanning electron microscopy was used to study these glands in females of the Southern Torrent Salamander, Rhyacotriton variegatus (Rhyacotritonidae), from northern California. Sperm initially enter the cloaca in a tangled mass from the spermatophore cap, but within the spermathecal tubules, small groups become aligned along their long axes. Sperm nuclei typically are embedded in apical microvilli of the secretory cells forming the distal acini of the spermathecae. Junctional complexes between apices of adjacent epithelial cells are occasionally broached or otherwise absent, and sperm can be found in the intercellular canaliculi between such cells. Spermathecae of R. variegatus are simple glands that branch off a tube extending dorsally into cloacal tissue. This spermathecal anatomy is in-between that of the Plethodontidae, which have a compound tubuloaveolar gland as the single spermatheca, and other saiamandroids, in which sperm storage occurs in numerous simple tubular glands, each one a spermatheca. Sperm associations in the simple spermathecae of R. variegatus, however, are most similar to those reported for plethodontids. [ABSTRACT FROM AUTHOR]

Abstract Sperm storage in cloacal spermathecae was studied in females of Triturus v. vulgaris from southern England killed at the end of the breeding season in June. This species mates and oviposits eggs in ponds from March to June. Included in the sample were 12 unmated females collected in terrestrial situations in March and mated in the laboratory. Some of these females oviposited viable eggs in the laboratory whereas others did not oviposit after mating. In addition, we examined five females with unknown mating histories that were collected from a breeding pond in June. We found that all of the specimens contained some stored sperm and were similar in spermathecal ultrastructure. The spermathecae exhibited characteristics of secretory epithelium at the end of a cycle, including irregular heterochromatic nuclei surrounded by scant cytoplasm, absence of organelles involved in synthetic activities, few secretory vacuoles, and wide intercellular canaliculi. Spermiophagy by the spermathecal epithelium was extensive. In contrast, spermathecae from females at the beginning of the breeding season as reported in our previous study were actively producing a PAS+ secretion and did not exhibit spermiophagy. Spermiophagy is a means of eliminating sperm prior to the next breeding season. [ABSTRACT FROM AUTHOR]

The anatomy and histology of the cloaca and spermatheca of 13 female smooth newts (Triturus vulgaris) were studied by light microscopy. The cloaca consists of a short, anterior tube (which receives the oviducts). which opens into a larger. more posterior chamber. The spermatheca, which is the only gland in the cloaca, consists of a mass of exocrine, acinar tubules which empty individually and dorsolaterally into the posterior part of the cloacal tube and all but the most posterior part of the cloacal chamber. Stored sperm are most abundant in the spermathecal tubules during the peak of the breeding season (in May and June); during their period of storage, the sperm do not appear to make intimate contact with the epithelial cells lining the spermathecal tubules. Long- term storage of viable sperm from one breeding season to the next is probably absent in the smooth newt. Sperm storage by and multiple insemination of females both occur in this species and are necessary preconditions for competition between the sperm of different males for the fertilization of eggs. However, sperm competition has not been demonstrated in the smooth newt. [ABSTRACT FROM AUTHOR]

Reproductive cycles of lizards have long been studied in both field and laboratory scenarios. However, comparisons of spermatogenic cycles and germ cell development strategies in different populations across a large geographic range have yet to be explored. The purpose of this study is to A) describe the spermatogenic cycle and germ cell development strategy of a population of Sceloporus consobrinus in southeast Louisiana, B) compare this cycle to a more northern population of this species, and C) compare the reproductive cycles of species within Sceloporus ( N = 21). In S. consobrinus from Louisiana, recrudescence begins in the fall (October and November), and the peak of spermatogenesis is reached the following spring/summer (May, June, July). This spermatogenic cycle is similar to that of a more northern population of S. consobrinus from Missouri. Within the genus Sceloporus, there are two seasonal patterns of spermatogenesis: initiation of spermatogenesis in the summer/fall and initiation of spermatogenesis in the spring. In both summer/fall and spring spermatogenic patterns, spermiogenesis occurs in the spring and may continue into the summer. The seasonal timing of recrudescence is an extremely plastic trait that has evolved multiple times throughout the Sceloporus clade. However, there appears to be an association of summer/fall and spring recrudescence with latitude. Tropical populations have a higher frequency of spring recrudescence and temperate populations have a higher frequency of summer/fall recrudescence. [ABSTRACT FROM AUTHOR]

The ampulla ureter and ampulla urogenital/uriniferous papilla represent differing morphologies of the caudal urogenital ducts in snakes. The ampulla ureter is an enlarged portion of the caudal extremity of the ureter that communicates the cranial regions of the ureter and the ductus deferens/Wolffian duct to the urodaeum. The ampulla urogenital/uriniferous papilla is an enlarged pouch, distinct from the ureter, which communicates the ureter and ductus deferens/Wolffian duct to the urodaeum. Although functional differences of these two structures are unknown, the ampulla urogenital/uriniferous papilla may have evolved for urine storage in males and females, and secondarily evolved a reproductive function in males. The most parsimonious optimization of the ampulla ureter and ampulla urogenital/uriniferous papilla indicates that the ampulla ureter is the ancestral state in snakes. Examining the presence or absence of the ampulla ureter and ampulla urogenital/uriniferous papilla in snakes on conflicting caenophidian phylogenies results in two hypotheses for the evolution of these variant morphologies: (1) The ampulla urogenital/uriniferous papilla evolved from the ampulla ureter independently in the Colubroidea and Elapoidea with subsequent losses of the ampulla urogenital/uriniferous papilla in the Elapoidea and (2) a single transition from the ampulla ureter to the ampulla urogenital/uriniferous papilla on the branch leading to the Colubroidea + Elapoidea with subsequent losses of the ampulla urogenital/uriniferous papilla in the Elapoidea and Colubroidea. The presence of the ampullae urogenital/uriniferous papilla in only the Colubroidea and Elapoidea highlights the affinity of these two taxonomic groups, a relationship that is strongly supported in published cladograms produced with molecular datasets. [ABSTRACT FROM AUTHOR]

This study investigates the evolution of snake spermatozoa within a phylogenetic context, with the addition of a new ultrastructural description from the spermatozoa of the Black Swamp Snake, Seminatrix pygaea. Overall the spermatozoon of S. pygaea is similar to that described for other squamates, whereas some characters such as the electron lucent space separating the cortex and medulla of the acrosome complex may be a unique feature of S. pygaea spermatozoa. This preliminary analysis of sperm evolution within Serpentes leads to the hypothesis that some sperm characters are more plastic than others. Incongruencies are found between the molecular and the morphological topologies utilized, and the phylogeny derived from a morphological data set recovers more unequivocal ancestral states of snake sperm structure. Characters such as the beginning of the fibrous sheath at mitochondrial tier one unite the Colubroidea, whereas characters such as the presence of an acrosome vesicle subdivision, absent vacuity subdivision, and round/oval mitochondria in transverse section unite all squamates. However, from this analysis it is evident that more taxa need to be studied and taxa with current data need to be more thoroughly investigated to make more conclusive remarks regarding the evolution of sperm structure within snakes. [ABSTRACT FROM AUTHOR]

The Mediterranean Gecko, Hemidactylus turcicus, is an invasive species found in warmer regions throughout the world, including the southern United States. In Louisiana, H. turcicus appears to be free of competition and has been rapidly expanding its range in the past several decades. However, in Florida and Texas, H. turcicus is heavily out-competed by closely related competitors that do not occur in Louisiana, including H. frenatus, of which a substantial amount of reproductive morphology and ecology is known. Although the reproductive cycle of H. turcicus has been studied in Florida and Louisiana, little is known about the seasonal variation of their oviduct and if they are capable of storing sperm, which can have substantial implications for reproductive competition. We analysed sperm production, storage and seasonal variation in the testes and oviducts of H. turcicus using light and electron microscopy. Previous studies found that female H. frenatus store sperm in the uterine-infundibular region for up to 36 weeks, and that their oviducts are active year-round. In H. turcicus, we found that sperm are stored in the uterine-infundibular region of the oviduct, and sperm are stored from May through August. Hemidactylus turcicus has one breeding season per year, producing three to four clutches between May and August, but between September and February minimal activity occurs in the oviduct. Additionally, male H. turcicus are producing sperm throughout the entire reproductive season, but whether females utilize stored sperm to fertilize eggs or if they mate continually throughout the spring and summer is unknown. [ABSTRACT FROM AUTHOR]

The germ cell development strategy during spermatogenesis was investigated in the black swamp snake ( Seminatrix pygaea) . Testicular tissues were collected, embedded in plastic, sectioned by ultramicrotome, and stained with methylene blue and basic fuchsin. Black swamp snakes have a postnuptial pattern of development, where spermatogenesis occurs from May to July and spermiation is completed by October. Though spatial relationships are seen between germ cells within the seminiferous epithelium during specific months, accumulation of spermatogonia and spermatocytes early in spermatogenesis and the depletion of spermatocytes and accumulation of spermatids late in spermatogenesis prevent consistent cellular associations. This temporal germ cell development within an amniotic testis is consistent with that seen in other recently studied temperate reptiles (slider turtle and wall lizard). These reptiles’ temporal development is more similar to the developmental strategy found in anamniotes than the spatial germ cell development that characterizes birds and mammals. Our findings also imply that a third germ cell development strategy may exist in temperate breeding reptiles. Because of the phylogenetic position of reptiles between anamniotes and other terrestrial amniotes, this common germ cell development strategy shared by temperate reptiles representing different orders may have significant implications as far as the evolution of sperm development within vertebrates. [ABSTRACT FROM AUTHOR]

The Eurycea bislineata complex ("two-lined salamanders") of eastern North America contains six described species, of which three have very similar morphologies and relatively broad geographic distributions, and three have more divergent morphologies with narrow geographic distributions. Recent molecular phylogenetic analyses found that four of the six species in the complex contain deep genetic structure, and that two of the species (E. cirrigera and E. wilderae) are paraphyletic in mitochondrial and nuclear DNA, inferring that current taxonomy does not reflect actual species boundaries in the complex. The member of this complex in the Sandhills physiographic region of south-central North Carolina, USA, is notable for its distinctive coloration and ecology, and a study on allozymic variation published over 30 years ago demonstrated that it is genetically distinct but clustered within the paraphyletic E. cirrigera. This study investigates the taxonomic status of the Sandhills population using morphology, mitochondrial DNA, and a 21-locus nuclear DNA data set to test if the Sandhills taxon represents a local ecomorph that is conspecific with adjacent populations of E. cirrigera, or if it represents a divergent evolutionary lineage that warrants taxonomic recognition. Mitochondrial and nuclear DNA revealed that the Sandhills taxon is genetically distinct and phylogenetically unrelated to adjacent populations of E. cirrigera. Principal components analysis of 316 adult specimens of the Sandhills taxon and the three morphologically similar species in the complex found considerable overlap among these taxa, but pairwise comparisons of heavily loading morphological characters showed that the Sandhills taxon usually has a shorter body, shorter tail, and narrower head. Based on these corroborated lines of evidence, the hypothesis that the Sandhills taxon represents only a local ecomorph is rejected and it is described as a new species. Clarification of the extent of its geographic range (including its possible presence in South Carolina), differentiation of larvae from other members of the complex, and verification of hypothesized narrow zones of hybridization with E. cirrigera at the peripheries of its geographic range are needed. The description of the Sandhills taxon brings the number of endemic salamander species in North Carolina to seven. Integrative taxonomic revisions of the E. bislineata complex, particularly E. cirrigera and E. wilderae, are needed to estimate species diversity and distributions of these salamanders more accurately. [ABSTRACT FROM AUTHOR]

Gladwyn Kingsley Noble was the first investigator to collectively examine courtship glands and correlate their function to the tail-straddling walk in plethodontid salamanders. While mental glands and caudal courtship glands have received the majority of attention since Noble's seminal work, Noble described other glands from Eurycea bislineata that were putatively involved in courtship that have received little or no attention (e.g., glands at the temporal regions of the heads of males). Previous studies demonstrated that heads of males enlarge during the mating season and some studies indicated that the enlargement was because of Noble's previously described temporal glands; however, current consensus of male head enlargement is that skeletal muscle hypertrophy is the cause of the head growth. In this study, we examined male and female E. bislineata throughout the year to test Noble's hypothesis that males possess courtship glands in the integument of the temporal regions of their heads and to assess what underlying tissues are involved with male head enlargement during mating. We found that the temporal regions of male heads change dramatically from non-mating to mating months, exemplified by two-dimensional geometric morphometrics. This variation is a result of M. levator mandibulae externus hypertrophy rather than glandular activity underlying the integument. Although no glandular masses isolated at the temporal regions of the heads result in this dynamic shape change, simple alveolar glands that resemble stereotypical courtship glands are found in the integument of only males from the mating season. These putative courtship glands are scattered amongst mucous and serous glands within the integument around the eyelids to at least the posterior termination of the cranium. The function of these glands is unknown but is probably involved with pheromone production, similar to more thoroughly examined courtship glands. [ABSTRACT FROM AUTHOR]

Previous studies demonstrated that variation in sperm morphology exists below the species level in a variety of organisms. However, most of the studies focus on invertebrates with only a few recent studies on vertebrates with a majority on birds and mammals. Understanding variation at various taxonomic levels is necessary for comparative studies. Therefore, to test the hypothesis that sperm shows little variation between and within closely related taxa, sperm morphology was analyzed in multiple populations of two sister species of lizards, Sceloporus consobrinus and Sceloporus undulatus. The ultrastructure of the sperm did not differ intraspecifically nor interspecifically, but differences were observed in sperm morphometrics between populations. The data gathered in this study show that the ultrastructure of the spermatozoa is consistent with other squamates, and although no variation was observed between the two taxa, slight variations were observed when compared to other members of Phrynosoma. The observed differences in sperm morphometrics show that sperm size differs despite variation in ultrastructure and there may be differences in selection on sperm size between the populations. [ABSTRACT FROM AUTHOR]

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 maturation in the elapid,Pelamis platurus, which were collected in Costa Rica in 2009. The spermatids ofP. platurusshare many similar ultrastructural characteristics to that described for other squamates during spermiogenesis. Three notable differences between the spermatids ofP. platurusand those of other snakes is a round and shorter epinuclear lucent zone, enlarged caudal nuclear shoulders, and more prominent 3 and 8 peripheral fibers in the principal and endpieces. Also, the midpiece is much longer inP. platurusand is similar to that reported for all snakes studied to date. Other features of chromatin condensation and morphology of the acrosome complex are similar to what has been observed inA. piscivorusand other squamates. Though the spermatids inP. platurusappear to be quite similar to other snakes and lizards studied to date, some differences in subcellular details are still observed. Analysis of developing spermatids inP. platurusand other snakes could reveals morphologically conserved traits between different species along with subtle changes that could help determine phylogenetic relationships once a suitable number of species have been examined for ophidians and other squamates. [ABSTRACT FROM AUTHOR]

Recent studies detailed the spermatogenic cycle of the Western Cottonmouth Snake,Agkistrodon piscivorusand noted that spermatogenesis is bimodal, with active periods during March-June and August-October in southeastern Louisiana. However, only spermatogonia were present in September in the only specimen that was captured and the authors state that the individual “should have a high testis volume and also show spermiogenic activity." The specimen in their study was caught immediately following Hurricane Katrina outside of its normal habitat. Therefore, in order to verify their assumption, individuals were captured during September of 2008 and the testes were spermatogenically active with spermatogonia, spermatocytes, and mature spermatozoa being present in the seminiferous epithelium of the testes. These data indicate that Hurricane Katrina could have had an impact on the spermatogenic cycle in Cottonmouths, resulting in stress-induced testicular regression. [ABSTRACT FROM PUBLISHER]

Over the past decade, studies on reproductive morphology in the Squamata (snakes and lizards) have expanded tremendously. With the accumulation of these studies and revisions of the terminology based on structural similarities and differences, it is imperative to review the work on tuataras to determine whether the structural organization fits the revised terminology of vertebrates. We investigated the morphology of the male reproductive system in the Tuatara, Sphenodon punctatus ( Rhynchocephalia), the sister taxon to the Squamata. Previous studies on the Tuatara used a nomenclature for the testicular ducts different from the current terminology for amniotes. The reproductive system in the Tuatara is consistent with reports in the Squamata. Two rete testis tubules exit the testis within a connective tissue sheath similar to that shown in other squamate species and the protherian Echidna. Each rete testis divides into multiple ductuli efferentes that fuse with the epididymis. The epididymis transitions into the ductus deferens where the sperm become more concentrated into spherical bundles. The ductus deferens enters the cloacal urodeum separately from the ureter. An ampulla ureter or ampulla urogenital papilla was not observed, which differs from previous studies of lepidosaurians. Furthermore, a sexual segment of the kidney ( SSK) was not observed, consistent with previous studies on the Tuatara. [ABSTRACT FROM AUTHOR]

Abstract: We studied spermiogenesis in the Mediterranean Gecko, Hemidactylus turcicus, at the electron microscope level and compared to what is known within other Lepidosaurs. In H. turcicus germ cells are connected via cytoplasmic bridges where organelle and cytoplasm sharing is observed. The acrosome develops from merging transport vesicles that arise from the Golgi and subsequently partition into an acrosomal cap containing an acrosomal cortex, acrosomal medulla, perforatorium, and subacrosomal cone. Condensation of DNA occurs in a spiral fashion and elongation is aided by microtubules of the manchette. A nuclear rostrum extends into the subacrosomal cone and is capped by an epinuclear lucent zone. Mitochondria and rough endoplasmic reticulum migrate to the posterior portion of the developing germ cell during the cytoplasmic shift and the flagellum elongates. Mitochondria surround the midpiece as the anlage of the annulus forms. The fibrous sheath begins at mitochondrial tier 3 and continues into the principal piece. Peripheral fibers associated with microtubule doublets 3 and 8 are grossly enlarged. During the final stages of germ cell development spermatids are wrapped with a series of Sertoli cell processes, which exhibit ectoplasmic specializations and differing cytoplasmic consistencies. The results observed here corroborate previous studies, which show the conservative nature of sperm morphology. However, ultrastructural character combinations specific to sperm and spermiogenesis seem to differ among taxa. Further studies into sperm morphology are needed in order to judge the relevance of the ontogenic changes recorded here and to determine their role in future studies on amniote evolution. [Copyright &y& Elsevier]

The testes of Hemidactylus turcicus are composed of seminiferous tubules lined with continuous germinal epithelia in which multiple germ cell morphologies can be found during the active months of sperm development. Spermatogenesis is quiescent during September, with only spermatogonia A and spermatogonia B present in the seminiferous epithelia and minimal mitotic activity is observed. Recrudescence begins in October and the early stages of spermatogenesis progress through November. The onset of spermiation is observed in December and continues through August with the heaviest sperm release occurring in June and July. Multiple generations of late elongated spermatids are found in association with early mitotic and meiotic cells during the months of December-August. This temporal germ cell development strategy is similar to that described in other squamates and anamniotes and is different from the spatial development exhibited by birds and mammals, in which germ cell populations collectively progress through the stages of spermatogenesis. The reptilian temporal model of germ cell development within a structurally amniotic testis leads to two hypotheses in character evolution: birds and mammals exhibit convergence of germ cell development strategy, or the spatial development strategy is a synapomorphy in amniotes, and reptiles represent an evolutionary reversal to the strategy employed by anamniotes. These findings, along with present and future data, may allow for more concrete phylogenetic analyses by creating more characters for phylogenetic matrices and may prove to be useful in future histopathological studies. [ABSTRACT FROM AUTHOR]

Previous investigators have described the spermatogenic cycles of numerous species of plethodontid salamanders. Most studies describe a fairly stereotypical cycle with meiotic divisions of spermatogenesis commencing in the spring/summer. However, many studies lack details obtainable from histological examination and/or testicular squashes and, instead, provide only mensural data from the testes. Studies that lacked microscopic evaluation often revealed spermatogenic cycles that varied greatly from that of the stereotypical cycle with meiotic divisions commencing in the fall/winter. Those studies hamper comparisons between the spermatogenic cycles of different species and their environments, as they do not provide a correlation between testicular size and any aspect of the spermatogenic cycle. In the following manuscript, we elucidate the spermatogenic cycle ofEurycea longicauda longicaudain an effort to outline an appropriate protocol for analyzing spermatogenesis in salamanders that will facilitate future comparative studies. Like many Nearctic plethodontids,E. l. longicaudaexhibits a meiotic wave that travels through the testes during the summer; this process is followed by spermiogenesis, spermiation, and recrudescence in the fall, winter, and spring. [ABSTRACT FROM PUBLISHER]