Reproductive biology of the Egyptian free-tailed bat, Tadarida Aegyptiaca
- Authors: Tsita, Johannes Ngoako
- Date: 1994
- Subjects: Tadarida aegyptiaca -- Reproduction , Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5754 , http://hdl.handle.net/10962/d1005442 , Tadarida aegyptiaca -- Reproduction , Bats -- Reproduction
- Description: The reproductive biology of Tadarida aegyptiaca was studied using specimens collected in the Cape Province of South Africa. The morphology of the reproductive tract of the species was generally similar to that of other molossids, however, the absence of Cowpers glands was unusual. Spermatogenesis began in February and spermatozoa were released to the cauda epididymis during August and September. Follicular development started in March and culminated with the appearance of Graafian follicles in July. Ovulation probably occurred in August and specimens were pregnant by September. Gestation length was estimated to be four to five months and a single young was born in December. The data suggest that T. aegyptiaca is monotocous and monoestrous.
- Full Text:
- Date Issued: 1994
- Authors: Tsita, Johannes Ngoako
- Date: 1994
- Subjects: Tadarida aegyptiaca -- Reproduction , Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5754 , http://hdl.handle.net/10962/d1005442 , Tadarida aegyptiaca -- Reproduction , Bats -- Reproduction
- Description: The reproductive biology of Tadarida aegyptiaca was studied using specimens collected in the Cape Province of South Africa. The morphology of the reproductive tract of the species was generally similar to that of other molossids, however, the absence of Cowpers glands was unusual. Spermatogenesis began in February and spermatozoa were released to the cauda epididymis during August and September. Follicular development started in March and culminated with the appearance of Graafian follicles in July. Ovulation probably occurred in August and specimens were pregnant by September. Gestation length was estimated to be four to five months and a single young was born in December. The data suggest that T. aegyptiaca is monotocous and monoestrous.
- Full Text:
- Date Issued: 1994
Immunolocalisation of, and ultrastructural changes in the LH gonadotropes of Miniopterus schreibersii and Rhinolophus capensis (Mammalia: Chiroptera) in relation to their reproductive cycles
- Authors: Bojarski, Christina
- Date: 1990
- Subjects: Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5589 , http://hdl.handle.net/10962/d1002039
- Description: LH gonadotropes are successfully identified in the anterior pituitary of Minioptems schreibersii and Rhinolophus capensis, using immunogold labelling at the light and electron microscopy level. The gonadotropes are oval to polygonal in shape and possess numerous small secretory granules, which contain LH throughout the year. Their distribution is similar in both species, although the abundance varies slightly between species and sexes. Seasonal changes are detected in gonadotrope ultrastructure, pituitary LH levels, and plasma hormone levels, and activity pattern of LH gonadotropes generally coincide with reproductive activity in both bat species. In female M. schreibersii gonadotrope activity, pituitary LH, and plasma LH levels coincide with development, implantation and gestation. During the delayed implantation gonadotropes are inactive and and high follicular period of plasma LH levels are low, coinciding with corpus luteum inactivity and low plasma progesterone levels. Implantation coincides with increased activity of the gonadotrope activity, increased plasma LH levels, reactivation of the corpus luteum and elevated plasma progesterone levels. Activation of LH gonadotropes towards the end of hibernation may be initiated by the winter solstice, which marks the change to increasing daylength. In female R capensis gonadotrope activity and high pituitary and plasma LH levels occur towards the end of follicular development. During hibernation gonadotrope activity and plasma LH levels decrease. Ovulation coincides with increasing gonadotrope activity (which follows the winter solstice), although a preovulatory peak in plasma LH is not detected. In male M. schreibersii and R. capensis, gonadotrope activity and high plasma LH and testosterone levels coincide with spermatogenesis, except during a period of reproductive inactivity in spring in male M. schreibersii, where gonadotropes appear active and plasma LH and testosterone levels are high. The reason for this apparent activity is not known. Male sperm storage during hibernation in male R. capensis coincides with low gonadotrope activity and low plasma LH and testosterone levels. Factors initiating gonadotrope activity and hence spermatogenesis are probably decreasing daylength (summer solstice) in M. schreibersii and increasing ambient temperatures and food abundance (following the hibernation period) in R.capensis.
- Full Text:
- Date Issued: 1990
- Authors: Bojarski, Christina
- Date: 1990
- Subjects: Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5589 , http://hdl.handle.net/10962/d1002039
- Description: LH gonadotropes are successfully identified in the anterior pituitary of Minioptems schreibersii and Rhinolophus capensis, using immunogold labelling at the light and electron microscopy level. The gonadotropes are oval to polygonal in shape and possess numerous small secretory granules, which contain LH throughout the year. Their distribution is similar in both species, although the abundance varies slightly between species and sexes. Seasonal changes are detected in gonadotrope ultrastructure, pituitary LH levels, and plasma hormone levels, and activity pattern of LH gonadotropes generally coincide with reproductive activity in both bat species. In female M. schreibersii gonadotrope activity, pituitary LH, and plasma LH levels coincide with development, implantation and gestation. During the delayed implantation gonadotropes are inactive and and high follicular period of plasma LH levels are low, coinciding with corpus luteum inactivity and low plasma progesterone levels. Implantation coincides with increased activity of the gonadotrope activity, increased plasma LH levels, reactivation of the corpus luteum and elevated plasma progesterone levels. Activation of LH gonadotropes towards the end of hibernation may be initiated by the winter solstice, which marks the change to increasing daylength. In female R capensis gonadotrope activity and high pituitary and plasma LH levels occur towards the end of follicular development. During hibernation gonadotrope activity and plasma LH levels decrease. Ovulation coincides with increasing gonadotrope activity (which follows the winter solstice), although a preovulatory peak in plasma LH is not detected. In male M. schreibersii and R. capensis, gonadotrope activity and high plasma LH and testosterone levels coincide with spermatogenesis, except during a period of reproductive inactivity in spring in male M. schreibersii, where gonadotropes appear active and plasma LH and testosterone levels are high. The reason for this apparent activity is not known. Male sperm storage during hibernation in male R. capensis coincides with low gonadotrope activity and low plasma LH and testosterone levels. Factors initiating gonadotrope activity and hence spermatogenesis are probably decreasing daylength (summer solstice) in M. schreibersii and increasing ambient temperatures and food abundance (following the hibernation period) in R.capensis.
- Full Text:
- Date Issued: 1990
Seasonal changes in the physiological and hormonal aspects of reproduction in the male long-fingered bat, Miniopterus schreibersii (Mammalia : Chiroptera)
- Authors: Paton, Joy Carol
- Date: 1989
- Subjects: Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5590 , http://hdl.handle.net/10962/d1002040
- Description: The reproductive cycle of Miniopterus schreibersii is modified as a consequence of a period of torpor/hibernation over the winter months. This bat is one of three genera which employ the reproductive strategy of delayed implantation in which the blastocyst remains free in the uterine lumen during the winter months. Spermatogenesis is initiated in February, with spermiogenesis occuring in March. Copulation, ovulation and fertilization takes place between March and May after which the testes regress and remain in an inactive condition until the following summer. Activity in the accessory gland complex is initiated in March and continues until early June. Plasma testosterone concentrations reach a peak in May, decline over the winter months and reach a second, unexplainable peak in October. Leydig cells are secretorily active in February/early March after which they undergo vacuolation and final degeneration. The question of the life cyle of Leydig cells is addressed and an increase in a certain cell after Leydig cell activity suggests that this cell type may be the precursor of Leydig cells.
- Full Text:
- Date Issued: 1989
- Authors: Paton, Joy Carol
- Date: 1989
- Subjects: Bats -- Reproduction
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5590 , http://hdl.handle.net/10962/d1002040
- Description: The reproductive cycle of Miniopterus schreibersii is modified as a consequence of a period of torpor/hibernation over the winter months. This bat is one of three genera which employ the reproductive strategy of delayed implantation in which the blastocyst remains free in the uterine lumen during the winter months. Spermatogenesis is initiated in February, with spermiogenesis occuring in March. Copulation, ovulation and fertilization takes place between March and May after which the testes regress and remain in an inactive condition until the following summer. Activity in the accessory gland complex is initiated in March and continues until early June. Plasma testosterone concentrations reach a peak in May, decline over the winter months and reach a second, unexplainable peak in October. Leydig cells are secretorily active in February/early March after which they undergo vacuolation and final degeneration. The question of the life cyle of Leydig cells is addressed and an increase in a certain cell after Leydig cell activity suggests that this cell type may be the precursor of Leydig cells.
- Full Text:
- Date Issued: 1989
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