赣昌鲫(日本白鲫♀兴国红鲤♂)的性腺结构观察

在繁殖季节与非繁殖季节采取解剖观察、组织切片等方法, 研究赣昌鲫(Carassius cuvierius♀Cyprinus carpio var. singuonensis♂)的性腺发育。经126尾鱼的解剖, 结果显示:赣昌鲫的性腺发育比较特殊, 性腺多为一侧发育或两侧不对称发育。在赣昌鲫的性腺部位大致有下列三个类型:(1)无性腺型(脂肪型):占24.6%, 为脂肪状, 没有性腺组织; (2)精巢型(包括以精巢为主体的两性嵌合体):占46.83%, 精巢小叶内分布有许多精子细胞, 或在曲细精管间隙中填充有多个不同发育阶级的卵母细胞, 大多数精子细胞发育异常、退化, 只有极少数正常成熟精子, 但挤压腹部, 始终没有精液流出, 显示为雄性不育; (3)卵巢型(包括以卵巢为主体的两性嵌合体):占28.57%, 卵细胞能发育到第Ⅲ时相, 到第Ⅳ时相时逐渐退化, 成熟的卵细胞少, 或在各发育时相卵细胞间隙中填充有精原细胞和败育的初级精母细胞, 解剖和挤压腹部始终观察不到排卵和卵粒流出, 同样表现为雌性不育。在精巢型与卵巢型的性腺中, 两性嵌合体型占总解剖数的36.51%, 其中以精巢为主的占25.4%、卵巢为主的占11.11%。       

Gonadal morphogenesis and sex differentiation in intraovarian embryos of the viviparous fish Zoarces viviparus (Teleostei, Perciformes, Zoarcidae): a histological and ultrastructural study

It is essential to know the timing and process of normal gonadal differentiation and development in the specific species being investigated in order to evaluate the effect of exposure to endocrine-disrupting chemicals on these processes. In the present study gonadal sex differentiation and development were investigated in embryos of a viviparous species of marine fish, the eelpout, Zoarces viviparus, during their intraovarian development (early September to January) using light and electron microscopy. In both sexes of the embryos at the time of hatching (September 20) the initially undifferentiated paired bilobed gonad contains primordial germ cells. In the female embryos, ovarian differentiation, initiated 14 days posthatch (dph), is characterized by the initial formation of the endoovarian cavity of the single ovary as well as by the presence of some early meiotic oocytes in a chromatin-nucleolus stage. By 30 dph, the endoovarian cavity has formed. By 44 dph and onward, the ovary and the oocytes grow in size and at 134 dph, just prior to birth, the majority of the oocytes are at the perinucleolar stage of primary growth and definitive follicles have formed. In the presumptive bilobed testis of the male embryos, the germ cells (spermatogonia), in contrast to the germ cells of the ovary, remain quiescent and do not enter meiosis during intraovarian development. However, other structural (somatic) changes, such as the initial formation of the sperm duct (30 dph), the presence of blood vessels in the stromal areas of the testis (30 dph), and the appearance of developing testicular lobules (102 dph), indicate testicular differentiation. Ultrastructually, the features of the primordial germ cells, oogonia, and spermatogonia are similar, including nuage, mitochondria, endoplasmic reticulum, and Golgi complexes.     

中国大鲵生殖腺胚后发育的形态学观察

为探寻中国大鲵(Andrias davidianus)生殖腺胚后发育的特点及规律,采用解剖学与组织学技术对其形态结构变化进行了观察.结果表明,大鲵的原始生殖腺开始出现于出膜28～49 d;出膜133～175 d时一些个体生殖腺内已初步分化出原始卵泡;出膜259 ～343 d时一些个体生殖腺内已初步分化出生精小叶;出膜427 d时,卵巢已明显分化为皮质与髓质,且髓质内出现了卵巢腔,精巢内生精小叶及其内的腔隙、精巢间质等分化已较为明显;出膜511 d时精巢分化为明显的生精小叶和非成熟小叶两个区域.本文认为,大鲵与其他无羊膜类原始生殖腺的分化一般发生在胚后阶段,而且雌性的分化时间早于雄性.     

Gonadal morphogenesis and sex differentiation in cultured Ussuri catfish Tachysurus ussuriensis

The objective of this study was to investigate the optimal developmental time to perform sex reversal in Ussuri catfish Tachysurus ussuriensis, to develop monosex breeding in aquaculture. Systematic observations of gonadal sex differentiation of P. ussiriensis were conducted. The genital ridge formed at 9 days post fertilization (dpf) and germ cells begin to proliferate at 17 dpf. The ovarian cavity began forming on 21 dpf and completed by 25 dpf while presumptive testis remained quiescent. The primary oocytes were at the chromatin nucleolus stage by 30 dpf, the peri‐nucleolus stage by 44 dpf and the cortical alveoli stage by 64 dpf. The germinal vesicle migrated towards the animal pole (polarization) at 120 dpf. In presumptive testis, germ cells entered into mitosis and blood vessels appeared in the proximal gonad on 30 dpf. The efferent duct anlage appeared on 36 dpf and formation of seminal lobules with spermatogonia and lobules interstitium occurred at 120 dpf. Therefore, gonadal sex differentiation occurred earlier in females than in males, with the histological differentiation preceding cytologic differentiation in T. ussuriensis. This indicates that undifferentiated gonads directly differentiate into ovary or testis between 17 and 21 dpf and artificial induction of sexual reversal by oral steroid administration must be conducted before 17 dpf.     

Gonadal morphogenesis and sex differentiation in the viviparous fish Chapalichthys encaustus (Teleostei, Cyprinodontiformes, Goodeidae)

This study describes the structural and ultrastructural characteristics of gonadal sex differentiation and expression of Vasa, a germline marker, in different developmental stages of embryos and newborn fry of the barred splitfin Chapalichthys encaustus, a viviparous freshwater teleost endemic to Mexico. In stage 2 embryos, the gonadal crest was established; gonadal primordia were located on the coelomic epithelium, formed by scarce germ and somatic cells. At stage 3, the undifferentiated gonad appeared suspended from the mesentery of the developing swimbladder and contained a larger number of germ and somatic cells. At stages 4 and 5, the gonads had groups of meiotic and non-meiotic germ cells surrounded by somatic cells; meiosis was evident from the presence of synaptonemal complexes. These stages constituted a transition towards differentiation. At stage 6 and at birth, the gonad was morphologically differentiated into an ovary or a testis. Ovarian differentiation was revealed by the presence of follicles containing meiotic oocytes, and testicular differentiation by the development of testicular lobules containing spermatogonia in mitotic arrest, surrounded by Sertoli cells. Nuage, electron-dense material associated with mitochondria, was observed in germ cells at all gonadal stages. The Vasa protein was detected in all of the previously described stages within the germ-cell cytoplasm. This is the first report on morphological characteristics and expression of the Vasa gene during sexual differentiation in viviparous species of the Goodeidae family. Chapalichthys encaustus may serve as a model to study processes of sexual differentiation in viviparous fishes and teleosts.     

Gonadal development and an indication of functional protogyny in the Indian damselfish (Dascyllus carneus)

The objective of this study was to determine the sexual pattern of the Indian dascyllus Dascyllus carneus . After an initially undifferentiated state, gonads of D. carneus developed an ovarian lumen and primary growth stage oocytes, and subsequently cortical-alveolus stage oocytes. From ovaries with cortical-alveolus stage oocytes and from more developed ovaries, some gonads redifferentiated into testes. From a sample of 163 individuals, two had a gonad containing degenerating vitellogenic oocytes and proliferating spermatogenic tissue, nine had a gonad containing degenerating cortical-alveolus stage oocytes and spermatogenic tissue, and five had a gonad with degenerating primary growth stage oocytes and spermatogenic tissue. The size of these individuals overlapped greatly with the size range of mature females, suggesting that at least in some individuals, redifferentiation toward a testis occurred after spawning as females. This indicates that D. carneus is a functional, diandric protogynous hermaphrodite. Removal of a dominant male(s) did not induce a sex change in any of the ranking females in the laboratory and field groups. There was no difference in the number of chases and signal jumps performed by the ranking female between control and experimental field groups, or before and after removal of the male. However, the sizes of the ranking females were at or beyond the size range of individuals with a mixed-stage gonad, suggesting that the developmental window for female-to-male sex change may not be open ended. In 41 of 43 field groups, in which sex of fish was determined histologically or by the shape of the urogenital papilla, one to several highest size ranks were occupied by males, followed by one to several females. Mature males, however, were not limited to the highest ranks and occurred at various lower size ranks within groups. Individuals with a mixed-stage gonad also occupied various size ranks within groups.     

The effect of inhibitors upon intracellular cyclic AMP levels and chick myoblast differentiation.

The small free-living nematode Caenorhabditis elegans is usually found as a hermaphrodite, but occasionally true males appear in the population. This study provides an account of gonadogenesis in the normal male and in a mutant that is a temperature-sensitive sex transformer.Male and hermaphrodite gonads develop from morphologically identical primordia. The small primordial gonad lies on the ventral side of the worm in the coelomic cavity. The gonadial primordium contains four nuclei at parturition. As this primordium develops in a hermaphrodite, it produces a double-armed, mirror symmetrical gonad that produces first sperm and then eggs. In the male, however, this primordium develops into an asymmetrical structure composed of a ventrally located testis, a loop region, a seminal vesicle, and a vas deferens. The male gonad presents a linear sequence of nuclei in successive stages of spermatogenesis beginning with a mitotic region in the testis, followed by clearly distinguishable stages of meiosis throughout the loop region to the seminal vesicle.A temperature-sensitive sex transformer mutant, tsB202, has been isolated. tsB202 carries an autosomal recessive mutation in linkage group II that at restrictive temperature transforms an XX hermaphrodite into a phenotypic male, complete with a normal male gonad and vestigial external genitalia. These transformed males are classified as pseudomales because they do not exhibit mating behavior. Temperature shift experiments have determined the specific temporal sequences of gonadogenesis, oogenesis, and spermatogenesis. Proper manipulation of the temperature regimen causes the production of intersexes. In one intersex, a male gonad complete with sperm, seminal vesicle, and vas deferens also contains oocytes. In another intersex produced by the complementary temperature shift, a hermaphrodite-shaped gonad develops that produces only sperm and no oocytes.     

Some aspects of the reproductive biology ofBarbus spp.,Capoeta damascina and their hybrids (Cyprinidae, Teleostei) in Israel

The reproductive biology and gonad cycle of three Cyprinid fish species:Barbus canis (Valenciennes, 1842),B. longiceps (Valenciennes, 1842) andCapoeta damascina (Valenciennes, 1842), in the upper Jordan River system of Israel were studied by monthly sampling over a two-year period. The reproductive activity of the three species was found to peak from January to April, mostly involving upstream migration towards spawning grounds on river beds 400–900 m above the Jordan River. Hybrids of the three species were collected in nature: in those ofBarbus canis ×Capoeta damascina, the gonads possessed both types of gametes, spermatogonia and oogonia, all of which became arrested at an early stage of development, and infertile; in hybrids of detected in nature, males had oocytes dispersed in the testis, whereas in females, the ovaries had small islets of spermatogonial tissue. In these female hybrids the oocytes ripened normally and spawning occurred.     

Patterns of reproductive morphology in the genus Gobiodon (Teleostei: Gobiidae)

The reproductive system of gobiid fishes (family Gobiidae), especially among hermaphroditic goby species, is morphologically diverse. Two hermaphroditic species in the genus Gobiodon, G. okinawae and G. oculolineatus, have several modifications of the gonoduct and gonad that are associated with secretion production and storage. In this study, an examination of six additional Gobiodon species, G. citrinus, G. fulvus, G. histrio, G. micropus, G. quinquestrigatus and G. rivulatus, revealed similar reproductive modifications. Among these six Gobiodon species, a number of features were found to be shared amongst each other and with G. okinawae and G. oculolineatus. All individuals had either an ovariform gonad or an ovotestis; no individuals had a purely testicular gonad. The gonadal lobes extended caudally past, rather than terminating at, their union with the gonoduct. Accessory secretory structures associated with the reproductive complex, termed accessory gonoduct structures, or AGdS, always originated from the gonoduct. The ovariform gonad was comprised entirely of ovarian tissue, while the ovotestis was divided into three morphologically distinct regions. Only one of the ovotestis regions was strictly gametogenic, consisting of both early stage oocytes and sperm-filled seminiferous lobules. The second region of the ovotestis was made up of stromal tissue surrounding some compressed lumina and a small number of early-stage oocytes. The third region was highly lobulated and acted as a storage region for eosinophilic secretions. Anteriorly, the stromal region of each of the two ovotestis lobes disappeared and the gametogenic and secretory storage regions of the ovotestis separated into two discrete lobes. In all of the examined Gobiodon species, all individuals having an ovotestis also had AGdS. However, AGdS presence among individuals having an ovariform gonad varied in a species-specific manner, with the AGdS being fully differentiated and well-developed in a number of species, and either in a very early stage of development, or absent, in others. The distribution of these AGdS states among Gobiodon species corresponds with that of several other morphological features that have been proposed by Harold et al. (Bull Mar Sci 82:119–136, 2008) as phylogenetically informative for intra-generic clade identification. Reproductive characters may prove informative in the development of hypotheses of relationships among gobiid fishes.     

Seasonal cycles of gonadal development and plasma sex steroid levels in Epinephelus morio, a protogynous grouper in the eastern Gulf of Mexico

In a field population of the protogynous red grouper Epinephelus morio in the eastern Gulf of Mexico, females with oocytes at all stages of development were collected during the spawning season suggesting that several batches of oocytes may be released over the spawning period. Plasma oestradiol (E₂) levels were highest in ripe females whose gonads contained both cortical alveoli and vitellogenic oocytes during the breeding season. Males were still spermiating as late as August, although levels of androgens 11-ketotestosterone (11-KT) and testosterone (T) had declined from their peaks in March. A few red grouper with either perinucleolar or cortical alveoli stage oocytes were undergoing sex change both during and after the spawning period. Low levels of E₂, T and 11-KT were detected in transitionals. Proliferation of male tissue was not restricted to any specific area of the gonad but occurred in pockets within the ovarian lumen. The sequence of an increase in gonial cells along the periphery of the lamellae, increase in interstitial tissue, degradation of female elements, and formation of a sperm duct seemed to be concurrent with spermatocyte proliferation and the process of preparing the gonad to function as a testis.     

Testicular development in the sea trout (Salmo trutta morpha trutta L.) after sex differentiation, with a reference to precocious maturation

Testicular development was followed in juvenile sea trout (Salmo trutta morpha trutta L.) stocked in a river near Szczecin, Poland in 1992. Fish age was between 3 and 6.5 months post‐hatch. Fish were sampled monthly. Sex‐dependent differences in gonad structure and timing of their differentiation were observed after dissection under light microscope. In 3‐month‐old fry, when female gonads were differentiating (morphologically and cytologically), gonads of potential males remained undifferentiated. Development of a gonad into a male was primarily indicated by the formation of seminiferous tubules (lobules). In the sea trout under study, the lobules formed between the fourth and fifth month post‐hatch (July–August) (fork length >5.6 cm). There were no significant differences in body fork length between fish with and without lobules, although mean length of the former was higher. Early spermatogenesis began once the type B spermatogonia appeared. The timing of their appearance differed widely among individuals. Type B spermatogonia were found for the first time in a 5‐month‐old male (late August). Spermatocytes and cells of subsequent stages appeared in an incompletely matured 6.5‐month‐old male as ‘attempted spermatogenesis’ (fork length = 8.8 cm). Most examined males remained immature, their germ cells not having passed the type A spermatogonium level. In 6.5‐month‐old alevins, no significant differences in fish size between individuals beginning spermatogenesis (stage II) and those at stage I were detected, although those at stage II were longer. As the male gonad structures were forming, the quantitative gonad parameters were gradually increasing, even when referring to the unit area; only the gonocyte size gradually decreased. Generally, each observed monthly or bimonthly difference was statistically significant (P < 0.05).     

The histology of mature gonads of Oreochromis (Nyasalapia) karongae (Trewavas)

Histology of gonads of Oreochromis karongae was undertaken to study internal cell characteristics during maturation. This study was necessitated by low spawning output of the fish species. Several oocyte stages, ranging from primary forms to vitellogenesis, suggest that the maturation was generally succesfully attained in the fish ponds. Pre‐vitellogenesis oocytes (oogonia to perinuclear stage) and more advanced vitellogenesis (primary vesicle to tertiary yolk vesicle) oocyte stages were all found in the same gonads. However, there were some discontinuities observed during stages 3 and 4, suggesting selective maturation. Failure of gonads to mature normally is attributed to an ecological crunch that was in a previous study associated with environmental factors. Atretic oocytes were also recorded in the same gonads, a sign that some oocytes failed to mature normally. This indicates insufficient stimuli for normal gonad development. Several stages of spermatogenesis (spermatocytes, spermatid and spermatozoa) were also found in the same gonads. Selective recrudescence was more pronounced in O. karongae because generally less oocytes attained final maturation stages compared to Oreochromis niloticus and other tilapias. This could be the main reason for low natural breeding that has been observed in both wild and captive stocks, and led to the abandonment of its use in aquaculture. This study corroborates findings of previous studies that depended solely on external gonad characteristics. Histology provides conclusive evidence from internal cell characteristics that other techniques are unable to show.     

A histological description of intersexuality in the roach

This paper is an illustrative guide to intersex in the roach Rutilus rutilus , based on 150 intersex individuals. Most intersex roach had female germ cells, or oocytes, within a predominantly male gonad (testis), and/or malformed/intersex reproductive ducts. The number, pattern and developmental stage of oocytes within testicular tissue in intersex fish varied greatly. In most intersex fish, a few primary oocytes, or numerous primary and secondary oocytes, were scattered randomly throughout the testicular tissue (multifocal intersex). In other, more severely feminized individuals, large areas of ovarian tissue were separated clearly from testicular tissue (focal intersex). Almost all intersex individuals had a female-like reproductive duct (ovarian cavity). In mild cases of intersex (in which the majority of the germ cells were male) the ovarian cavity was present together with the male sperm duct/vas deferens, whilst in certain severe cases, the sperm duct was absent or vestigial.     

Patterns of structural change in gonads of the divine dwarfgoby Eviota epiphanes as they sexually transition

This study documents changes in gonadal structure for the serial hermaphrodite (or bidirectional sex changer) divine dwarfgoby Eviota epiphanes (family Gobiidae) as individuals transition in both directions. To evaluate transitional gonad morphology, individuals actively producing the same gamete type (oocytes or sperm) were set up into pairs and euthanised over a period of 14 days to get a time series of morphological changes during gonad transformation. Results from this study show that rapid changes in the gonad take place at a structural level as individuals change their reproductive function and gamete production. Changing from oocyte production (o-phase) to sperm production (s-phase) starts with the breakdown of vitellogenic oocytes (i.e., atresia) followed by the appearance and proliferation of spermatogenic tissue which, in most cases, was not previously visible. Changing from sperm production to oocyte production included the cessation of sperm production, a reduction in size and number of seminiferous lobules and the maturation of previtellogenic oocytes already present in the gonads. Experimental fish changed from oocyte production to sperm production more readily than from sperm production to oocyte production. The hypothesis that shifts in sexual function among serially hermaphroditic fish species have a similar cost in either direction is not supported in E. epiphanes.     

Ultrastructure of the gametogenesis of the common Mediterranean starfish,Echinaster (Echinaster) sepositus

Echinaster (Echinaster) sepositus is one of the most abundant sea stars in western Mediterranean rocky bottoms, yet its reproductive biology remains virtually unknown. Here we report the ultrastructure of its gametogenesis over 2 consecutive years. It is a gonochoric species with an annual reproductive cycle spawning gametes in late summer and early autumn. Each arm of every individual contained two gonads (dark red in females and yellow in males). In both sexes, the gonad was a single, large sac composed of several smaller sacs. The gonad wall consisted of two multilayered sacs, outer and inner, separated by the genital haemal sinus. The histology of the gonad wall was consistent with that found in other asteroids. Oogenesis was continuous during the year, but eggs were spawned only in late summer. Oocytes were in close relationship with follicular cells that are suggested to transfer nutrients to the oocytes. Spermatogenesis was restricted to 5–6 months in spring-summer. It occurred in columns with an axial interstitial cell supporting each column, and producing processes towards the lumen that remained connected to spermatogenic cells by intercellular junctions. Developing sperm cells were found along the length of the column, while spermatozoa were found free in the testis lumen. Spermatogenesis followed the pattern described for echinoderms, to give rise to an acrosome-bearing, round-shaped spermatozoon. The histology and cytology of the reproductive process in E. sepositus followed the general pattern found for asteroids.     

Cloning and expression analysis of piRNA-like RNAs: adult testis-specific small RNAs in chicken

Many small RNAs have been cloned from animal gonads, for example, endogenous small interfering RNAs (endo-siRNAs) were found in oocytes and piwi-interacting RNAs (piRNAs) were found in testis. Gallus gallus (chicken) is an important model organism, but few small RNAs have been identified from its gonads. In this study, we isolated and cloned 156 small RNAs from adult chicken testes. Since there is a reasonably even distribution from 22 to 33 nt, these small RNAs are slightly longer than miRNAs and endo-siRNAs. Genome mapping indicated that these small RNAs were derived from intergenic regions, exons, introns, and repetitive elements including chicken repeat 1, long terminal repeats, and simple repeats. Since they are similar with piRNAs, we named them piRNA-like RNAs (pil-RNAs). Northern blotting of 16 selected sequences showed that nine are specifically expressed in the adult testis. The vast majority of these pil-RNAs are poorly conserved between species, suggesting that they are unique to the adult chicken testis. Further analysis of the cloned pil-RNAs will improve our understanding of the function of small RNAs in animal gonad development.     

Histological study of the development and sex differentiation of the gonad in the European eel

The histological structure of the gonads was studied in yellow eels sampled from a coastal lagoon and from stocks reared in an aquaculture plant showing different sex ratios. Gonad development related to body size rather than to age and underwent an intermediate stage characterized by a structure of an early testis but containing oogonia and oocytes. This gonad was called the Syrski organ and the stage juvenile ambisexual. Ovaries were found in eels from 22–30 cm in length, possibly derived from undifferentiated gonads or from Syrski organs. Fully differentiated testes were found in eels >35 cm, derived from Syrski organs. These observations support the results of previous research. From elvers and in eels up to 15–16 cm in length, growth of the gonadal primordium is due to primordial germ cell migration. In eels > 15 cm multiplication of primordial cells begins. Oogonial clones were found in eels > 18 cm in length, whilespermatogonium B clones were observed in eels >30 cm in length. The dynamics of sex differentiation was different among stocks with different ultimate sex ratios: ovaries were found in shorter eels in stocks with a prevalence of females, in longer eels in stocks with a prevalence of males. This result supports the hypothesis of a metagametic (environmental) sex determination. The somatic cells in contact with germ cells and those in the interstitium appeared early during gonad development and preceded germ cell differentiation. This suggests that somatic cells are the targets of the environmental factors influencing sex differentiation.