• Korean Journal of Animal Reproduction
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• v.9 no.1
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• pp.46-55
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• 1985

In order to investigate the spermiogenesis of the Korean goat, the tissue obtained from the testis and the epididymis of eight matured bucks were conventionary prepared as thin sections and these sections were observed under a transmission electron microscope. Based on the development of the varous permanent organelles and certain transient structures, the spermiogenesis of the Korean goat could be divided into four main phases: Golgi, cap, acrosome and maturation; and these phases had been further subdivided into a total of nine stages. There was abundance of the contents of acrosomal vesicle contained ring-shaped material surrounding the acrosome in the early cap stage. The mitochondria made the mitochondrial sheath started from the annulus towarding the neck and formed helical arrangement in the mid maturation stage, The postacrosomal denselamina was a, pp.ared to be wave-shape in the late maturation stage. The spermiogenesis of the Korean goat was found to be basically similar to that of the Korean cattle.

• Development and Reproduction
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• v.10 no.1
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• pp.9-17
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• 2006

The cycle of the seminiferous epithelium and morphological features of spermatids in Crocidura dsinezumi were studied by light microscopy. The cycle of the seminiferous epithelium was divided into 12 stages. The dark type of spermatogonium(Ad) is appeared in all stages, and intermediate(In) in stage IV and B spermatogonium in stage V and VI were observed. The development of the acrosomal system, and changes in nuclear morphology of spermatids were divided into 14 steps. The Golgi, cap, acrosomal, maturation and spermiation phases were observed during steps $1{\sim}2$, steps $3{\sim}6$, steps $7{\sim}10$, steps $11{\sim}13$, and step 14, respectively. Our results provide the foundation for future studies of the spermiogenesis of Crocidura dsinezumis.

• Korean Journal of Veterinary Research
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• v.32 no.3
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• pp.281-293
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• 1992

Classification of the cycle of seminiferous epithelia into 12 stages by the morphological changes in acrosomal system and evaluation of the relative frequency of stages and the cell association were histologically performed in the mature Korean native Jin-do dogs. The results were summarized as follows; 1. The minimum number of type A spermatogonia averaged 1.01 at stages I, while maximum number averaged 2.47 at stages XII. Some type A spermatogonia divided at stage XII to produce the type intermediate(IN) spermatogonia at the following stage I. The type IN spermatogonia divided at stage IV to produce the type B spermatogonia at stage V. 2. The type B spermatogonia divided at stage VI to produce the preleptotene primary spermatocytes at stage VII. The secondary spermatocytes observed at stage XII. The secondary spermatocytes observed at stage XII divided to give rise to the round spermatids at the following stage I. The numbers of the first spermatocytes and spermatids were almost constant, respectively, through all the cycles of seminiferous epithelium. 3. The acrosomal vesicle was invaginated to occupy one third to half of spermatid nucleus at the cap phase, which was different from that of rodent and ruminant spermatid nuclei. 4. The relative frequencies of stages I to XII of seminiferous epithelia cycle were 10.34, 4.84, 5.03, 8.22, 10.86, 6.63, 6.42, 18.88, 10.17, 6.18, 7.62% and 4.81%, respectively.

• The Korean Journal of Malacology
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• v.26 no.3
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• pp.235-244
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• 2010

Ultrastructural characteristics of the testis and spermatogenesis of Crassostrea gigas were investigated by Transmission and Scanning Electron microscope observations. The testis is a diffuse organ consisting of branching acini containing differentiating germ cells in a variety of stages. The acinus is surrounded by an intermitent layer of myoepithelial cells andis divided into subcompartments that are partially separated by pleomorphic accessory cells which remain in close contact with germ cells until late stages of development. these accessory cells contain a large quantity of glycogen particles and lipid droplets in the cytoplasm. Therefore, it is assumed that they are involved in the supplying of the nutrients for germ cell development, while any phenomena associated with phagocytosis of undischarged, residual sperms by lysosomes could be find in the cytoplasm of the accessory cells. The morphology of the spermatozoon has a primitive type and is similar to those of other bivalves. Mature spermatozoa consist of broad, cap-shaped acrosomal vesicle, subacrosomal material (containing axial rod embedded in a granular matrix), a oval nucleus showing deeply invaginated anteriorly, two triplet substructure centrioles surrounded by four spherical mitochondria, and satelite fibres appear to the distal centriole and plasma membrane. Spermatozoa of C. gigas resemble to those of other investigated ostreids. In particular, the anterior region of the acrosomal vesicle is transversely banded. It is assumed that differences in this acrosomal substructure are associated with the inability of fertilization between the genus Crassostrea and other genus species in Ostreidae. Therefore, we can use sperm morphology in the resolution of taxonomic relationships within the Ostreidea. The spermatozoon is approximately $42-47{\mu}m$ in length including an oval sperm nucleus (about $0.91{\mu}m$ in length), an acrosome (about $0.42{\mu}m$ in length) and tail flagellum ($40-45{\mu}m$). The axoneme of the sperm tail flagellum consists of nine pairs of microtubules at the periphery and a pair at the center. The axoneme of the sperm tail shows a 9 + 2 structure. These morphological charateristics of acrosomal vesicle belong to the family Ostreidae in the subclass Pteriomorphia.

• Applied Microscopy
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• v.31 no.2
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• pp.129-141
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• 2001

To investigate the spermiogenesis of the Saghalien Pygmy shrew (Sorex minutus gracillimus), the testis obtained from mature male shrew was studied by electron microscopy, and the following results obtained based on the morphological characteristics of cell differentiation of the seminiferous epithelium in the testis. According to the fine structural differentiation, spermiogenesis of S. minutus gracillimks was divided into Golgi, cap, acrosome, maturation and spermiation phases. Beside, the Golgi and cap phases were subdivided into three steps of early, middle and late phase respectively, and acrosome phase into two steps of early and late phase , and maturation and spermiation phases has only one step respectively. Thus, the spermiogenesis of S. minutus gracillimus was divided into a total of ten steps. The chromatin granules begin to be condensed in the acrosome phase, and a perfect nucleus of sperm was formed at the spermiation phase. Mancette were appeared from the late acrosome phase to the maturation phase. The formation of sperm tail began to develop in the late Golgi phase, and completed at the spermiation phase. Multivesicular bodies were appeared from the Golgi phase to the maturation phase, recognized with pale, pale and moderate, and dense at Golgi, cap and acrosomal and matulation phases respectively.

• Biomedical Science Letters
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• v.11 no.4
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• pp.545-553
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• 2005

The present study provides descriptions of the cellular associations of the seminiferous epithelium cycle in the Crocidura shantungensis. The cycle of the seminiferous epithelium was divided into 14 stages, and developing spermatids were subdivided into 15 steps. The Golgi phase occurs the first two steps, and the cap phase had the next four consecutive steps. The acrosomal and maturation phases were consisted of steps $7\~14$, and the remaining one step consisted the spermiation phase. The Ad type of spermatogonia was observed whole stages, and Ap, In and B spermatogonia were observed from stage II to stage VI. The preleptotene, leptotene and zygotene of primary spermatocytes were observed from VII to XIV stages, and pachytene spermatocyte was observed from I to XII stages. The diplotene spermatocyte was observed XIII stages, and meiotic figures and secondary spermatocytes were observed stage XIV. Our results provide the foundation for a variety of future studies of the spermiogenesis of C. shantungensis.

• Korean Journal of Animal Reproduction
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• v.12 no.1
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• pp.1-10
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• 1988

In order to investigate the spermiogenesis of the Korean Native Jin-do dog, the tissue sampled from the testis and the epididymis of matured dog were conventionally prepared as thin sections. And then these sections were observed under a transmission electron microscope. Based on the development of various permanent organelle and certain transient structures, the spermiogenesis of the dog could be divided into four major phases: Golgi, cap, acrosome and maturation; and these phases had been futher subdivided into seven stages. In the maturatin phase, the karyoplasm has been condensed completely and the nucleus eleongated as the movement of the unclear ring. The equatorial segment has notable waist-form at the late acrosomal stage. In the cross section of the tail, it shows a typicl 9＋9＋2 pattern of the axial fiber bundle condisting of the dense fibers, the inner fibers, and a central pair. The dense fiber number 1, 5, 6, and 9 were larger in diameter than the rest of the dense fibers.

• Applied Microscopy
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• v.17 no.1
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• pp.1-15
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• 1987

Testes from the allied rock wallaby(Petrogale assimilus) have been examined by the electron microscopy in thin sections in order to examine spermiogenesis and structure of spermatozoa. The spermiogenesis can be divided into nine stages: early Golgi, late Golgi, collapsing, nuclear protrusion, condensation and flattening, nuclear shaping, rotation, nuclear ring contraction, and maturation. The acrosome has been abruptly formed following the collapse of expanded acrosomal vesicle without the cap stage described in the eutheria. The flatly condensed nucleus rotates obliquely to the axis of the axial filament complex and the folded acrosome covers the anterior third of the dorsal nuclear surface forming a wide subacrosormal space as the nuclear ring has contracted. The Sertoli cell reaction and spur are prominent during the nuclear protrusion and rotation stages. A mature spermatozoon has S-shape head which has an extended part reaching to the vicinity of the middle piece.

• Applied Microscopy
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• v.33 no.1
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• pp.25-39
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• 2003

Cell differentiation and ultrastructural characteristics in the seminiferous epithelium of Myotis macrodactylus was investigated with the light and electron microscopes. Spermatogenesis has begun at April and finished at September. The nuclei of A spermatogonia (dark and pale type of spermatogonia) were oval, applied to the basal lamina, and surrounded by Sertoli cells. By comparison with other types of spermatogonia, the cell and nucleus of B type of spermatogonium is globular and larger than A types of spermatogonia. The nucleolus appears as a coarse and touches the nuclear membrane. The cell and nucleus of spermatocytes was globular and larger, but primary spematocyte is larger than secondary spermatocyte. Spermiogenesis was divided according to the level of fine structural difference, into Golgi, cap, acrosomal, maturation and spermiation phases; Golgi, cap, acrosomal and spermiation phases were further subdivided into steps of early and late phase respectively, and maturation phase has only one step. Hence, the spermiogenesis has been divided into a total of nine phases. In the change of karyoplasm, the chromatin granules are condensed at late Golgi phase and completed at spermiation phase. The sperm tail began to develop in early Golgi phase and completed in spermiation phase. The process of degeneration of spermatogenic cells in the seminiferous tubules was continually observed from October, before the beginning of hibernation, to hibernation phase (November, December, January, February, March). Immatured spermatogenic cells in the seminiferous tubules have been engulfed by phagocytosis of Sertoli cells during period of degeneration. It is deduced that the adaptative strategy serves as the mechanism to regulate the effective use of energy to prepare for long hibernation and regulation of breeding cycle.

• Biomedical Science Letters
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• v.13 no.1
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• pp.61-69
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• 2007

The cycle of the seminiferous epithelium and the development of spermatids of Apodemus agrarius coreae were observed using a light microscope. The cycle of the seminiferous epithelium was divided into 10 stages, and developing spermatids were subdivided into 10 steps. The Golgi phases occurs the first two steps ($St_1,\;St_2$), and the cap phases had the next two consecutive steps ($St_3$ and $St_4$). The acrosomal phases consisted of steps $5{\sim}8$ ($St_5-St_8$), and the remaining two steps consisted the maturation ($St_9$) and spermiation ($St_{10}$) phases, respectively. Type Ad spetmatogonia are appeared in all stages (I-X). Type Ap spermatogonia appeared from stage I and II, In spermatogonia from stage III, IV and V, and B spermatogonia from stages VI. The leptotene spermatocytes appeared from stage VII, zygotene from stages I, II, VIII, IX and X, pachytene from stage III to VIII, diplotene in stage IX, and meiotic figures and secondary spermatocytes in stage X. These data are considered in relation to interspecific differences in sperm morphology.