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1.
沙棘木蠹蛾生殖系统形态学和组织学观察   总被引:1,自引:0,他引:1  
周娇  李娟  翁强  骆有庆 《昆虫知识》2012,49(6):1629-1635
沙棘木蠹蛾Holcocerus hippophaecolus Hua,Chou,Fang et Chen属鳞翅目(Lepidoptera)木蠹蛾科(Cossidae),是我国的特有种.2001年以来,沙棘木蠹蛾在我国大面积爆发,是屹今为止我国沙棘林最大的蛀干害虫,给我国的沙棘产业造成了巨大的损失.本论文从形态学和组织学2个方面确定了沙棘木蠹蛾雌、雄生殖系统的特征,同时,对比了雄性交尾前后生殖系统各部位的差异.未交尾雄蛾的生殖系统贮精囊、附腺管和射精管呈白色,其内包含大量的精子束待交尾,已交尾雄蛾的生殖系统呈透明或半透明状.除雄性附腺外,在交尾后的精巢、贮精囊和射精管中都能观察到真核精子束.通过上述对雄性生殖系统的形态学和组织学观察,尤其是对贮精囊和射精管中精子束观察,可判断精子束的填充状态,从而判断雄蛾交尾与否,能够检验性信息素引诱剂对沙棘木蠹蛾的防治效果,确立判断雄蛾交尾与否的标准对指导沙棘木蠹蛾防治具有重要意义.  相似文献   

2.
针对目前关于草地螟Loxostege sticticalis L.雄成虫生殖系统结构和功能的研究相对缺乏的状况,本文利用光镜和扫描电镜系统研究了草地螟雄蛾的内外生殖器官及相关结构。草地螟雄蛾内外生殖器官集中于腹部第510腹节;内生殖器官位于510腹节;内生殖器官位于58腹节内腔中,由睾丸(testes)、贮精囊(seminal vesicle)、输精管(vas deferens)、附腺(accessory gland)和射精管(ejaculatory ducts)组成;外生殖器官为腹部第9、10腹节的特化结构,包括抱握器(harpes)、背兜(tegumen)、基腹弧(vinculum)、钩形突(uncus)、颚形突(gnathos)、阳茎囊(aedeagal caecum)和阳茎(phallus)。外生殖器中抱握器的端刺(furcella)方向为雄蛾区别于其它种类的一个重要形态学特征。该研究首次明确了草地螟雄蛾的生殖系统结构,并为锥额野螟蛾属中种间分类提供更多的科学依据。  相似文献   

3.
橙黄豆粉蝶生殖系统形态学研究   总被引:6,自引:1,他引:5  
解剖并描述了橙黄豆粉蝶Colias fieldii Ménétriés的生殖系统结构。结果表明:橙黄豆粉蝶雄性内生殖器包括精巢(睾丸)、2个贮精囊、2条输精管、1对复射精管、2根附腺和单射精管。其中2个睾丸体彼此密接似单一器官包被在半透明的睾丸膜中,单射精管较长且分化为形态不同的4段。外生殖器包括抱器瓣、阳茎及其附属结构;雌性内生殖器由1对卵巢、2根侧输卵管、1根中输卵管、肾型受精囊、附腺、外生殖腔及产卵孔组成。卵巢左右对称,每个卵巢具4根多滋式卵巢管。外生殖器包括导精管、囊导管、交配囊及其附属结构、前后表皮突和肛突。  相似文献   

4.
【目的】揭示日龄和交配对亚洲玉米螟Ostrinia furnacalis雄蛾内生殖器官的影响,以及亚洲玉米螟雄蛾的交配状态和性信息素诱捕之间的关系。【方法】采用行为学和生殖器解剖技术,研究不同日龄和交配状态亚洲玉米螟雄蛾内生殖器特征,并将其与田间性信息素诱捕雄蛾进行比较。【结果】除了精巢、输精管、储精囊、附腺、复射精管和单射精管外,亚洲玉米螟雄蛾内生殖系统还包含1对附腺囊,同时单射精管非角质化区分为5段(PS1-5),PS1又细分为5区(PS1Ⅰ-Ⅴ)。生殖器内含物可分为5级(0-4级),存在充满和未充满生殖器两种状态。1日龄雄蛾内生殖系统不同器官的内含物等级存在差异,但是日龄对雄蛾生殖系统内含物等级无明显影响。交配后0 h亚洲玉米螟雄蛾,除输精管、储精囊和附腺囊外,其余生殖器官内含物等级较未交配雄蛾的均发生显著变化。随着交配后时间的增加,雄蛾生殖器内含物等级逐渐恢复,各器官内含物等级恢复的速度存在差异,交配后60 h所有内含物等级均恢复到未交配状态。但是直到交配后228 h,交配雄蛾PS5内含物仍然表现出断裂等形态特征,和未交配雄蛾存在差异。性信息素引诱雄蛾中有60.9%的生殖系统表...  相似文献   

5.
拟澳洲赤眼蜂(Trichogramma confusum)的体长约0.6mm,腹部长度约0.3mm.雌蜂生殖系统(包括卵巢、生殖腔、受精囊及三种附腺)位于腹部后端,约占腹腔的2/3.成熟的卵巢由两条多滋式的卵巢管组成.两条成熟卵巢的端段细长,扭卷成一条疏松索,基部膨大,内脏贮存大量卵粒.成对的侧输卵管较短,分别开口于生殖腔后方的两侧,中输卵管缺如.受精囊呈梨形,开口于生殖腔后方.雌性生殖系统三种附腺中,第一种附腺是成对的,呈锤状,分别连接于生殖腔前方两侧;第二种附腺,腺体呈球状,其前端以短曲的小管通进膨大的贮腺囊,贮腺囊端部成柄状的弯曲小管,连接于产卵管的基部开口处.第三种附腺的腺体呈棒状,前端为细长的小管,开口于第二种附腺贮腺囊的前端.雄性生殖系统由成对的睪丸,输精管、贮精囊、附腺及单一的射精管组成.蛹的早期到后期至成虫期睾丸的形态结构,各有不同变化.  相似文献   

6.
小地老虎生殖系统的研究   总被引:2,自引:0,他引:2  
卢筝 《昆虫学报》1982,(3):268-274
小地老虎Agrotis ypsilon Rott.是农业上的重要害虫。本文对其雌性和雄性的内部和外部生殖器官,作了形态研究,以供防治和测报工作者参考。 小地老虎雄性内生殖器包括:一个扁圆形的睾丸;睾丸腹面连接一对S形的、两端粗中央细的贮精囊;贮精囊的前端各连接一条输精管;输精管的末端与S形的复射精管相连接;复射精管的前端连接两条细长的性副腺,复射精管的后端合拢形成一条很长的单射精管;单射精管分前段与后段两个部分,单射精管的末端连接阳茎囊。 雄性外生殖器 钩形突长钩形;颚形突与肛管腹壁愈合;尾突缺如;背兜屋脊状;基腹弧短;囊形突极小。抱握器钳状:抱器背缘在前端凹入甚深,抱器腹缘在前端1/3处外突出是种的特征;抱器端有一列冠刺;铗片基部粗,前端长形的薄片;腹突小。阳茎短粗,阳茎轭片从侧面观呈三角形。 雌性内生殖器具一对卵巢,每一卵巢有4根卵巢管;两条侧输卵管汇合成一条中输卵管,与外生殖腔相连接。受精主囊镰刀形;副囊瓜子形,二者镶嵌在一起,受精管通到中输卵管基部;受精囊腺细长。附腺具有一小形的主囊和一对较大的附腺囊,其端部伸出细长的附腺。 雌性外生殖器 肛乳突末端尖,前生殖突比后生殖突显著的短,交配囊盘绕成环形,囊导管短;精球与交配囊体和囊颈总长度同长。  相似文献   

7.
亚洲柑橘木虱Diaphorina citri Kuwayama是柑橘黄龙病的传播媒介。本文利用Ste REO Discovery V20体视显微镜对亚洲柑橘木虱成虫内生殖系统进行解剖观察,并探索了亚洲柑橘木虱雌雄成虫内生殖系统的形态变化规律。结果表明:雄虫内生殖系统由1对精巢、1对输精管、1个精泵、1个射精管、1对附腺和1个贮精囊组成。雌虫内生殖系统由1对卵巢、1对侧输卵管、1个中输卵管、2个附腺、1个黏腺和1个受精囊组成。交配前期和交配期的雄虫精巢饱满,精巢在交配后期明显萎缩。交配期和交配后期的雄虫贮精囊都明显大于交配前期的贮精囊。雌虫受精囊在交配前期、交配期和交配后期依次增大,交配前期的受精囊呈不饱满状态,交配期和交配后期受精囊呈饱满状态,内有白色精包。交配后期的雌虫卵巢内有大量成熟的橙黄色卵。  相似文献   

8.
粘虫(Pseudaletia separata(Walker))生殖系统的解剖   总被引:2,自引:0,他引:2  
何继龙 《昆虫学报》1963,(3):282-291
本文内容是研究粘虫(Pseudaletia separata(Walker)生殖系统的形态构造。全文分为雄性内部生殖器、雄性外部生殖器、雌性内部生殖器及雌性外部生殖器四部分。 粘虫的雄性内生殖器中, 有睾丸一对, 左右并列, 呈扁椭圆形, 外被紫红色睾丸膜; 输精管一对, 基部膨大成二对贮精囊; 射精管分成复射精管及单射精管两部分。雄性外生殖器的构造极为复杂, 第9腹节的背、腹板分别形成马鞍状的背兜及基腹弧; 第10腹节仅有其附肢特化成钩形突、颚形突和背兜侧突等; 抱握器占雄性外生殖器中的大部分, 其顶上角具长约1毫米的端刺一枚, 此为本种特征之一, 可以此与近似种区别; 阳茎由基部球状的阳茎囊和端部柄状的阳茎端组成, 内具内阳茎及角状器:雄性外生殖器中有关器官的肌肉来源亦作了叙述。 精液是以贮存于精球的方式授入雌体, 精球分为精球体、精球柄及系带三部分。 雌性内生殖器中, 卵巢为多滋式, 一对, 各由四个卵巢管组成, 两组卵巢管再与一对侧输卵管相连, 后者通入中输卵管中, 中输卵管后端连有外生殖腔, 其外方的开口是为产卵孔; 受精囊为长形梨状物, 分成主囊及副囊两部分, 两者在顶部愈合, 并由此发出受精管与外生殖腔相通, 在主囊顶端有受精囊腺; 附腺一对, 与附腺囊相连, 后者通入附腺主囊, 并由此开口入外生殖腔。雌性外生殖器是由交配囊和产卵器组成, 前者复可分成囊导管、囊体及囊颈三部分, 其外方的开口为交配囊孔, 有导精管从囊颈连于外生殖腔; 产卵器由第8、9腹节组成, 非呈特殊构造。  相似文献   

9.
长足大竹象生殖系统的形态解剖研究   总被引:1,自引:0,他引:1  
解剖研究了长足大竹象雌雄虫牛殖系统的构造.该虫的雌性生殖系统包括一对卵巢、一对侧输卵管、中输卵管、交配囊、受精囊、生殖腔、产卵器;雄性生殖系统由一对睾九、一对输精管、一对附腺、射精管和交配器组成.  相似文献   

10.
铃虫交配过程中精子的转移   总被引:1,自引:0,他引:1  
统计了棉铃虫交配前后贮精囊、复射精管和精包内真核精子(束)的数量,以此来验证棉铃虫交配过程中是否存在精子回流现象。结果表明,棉铃虫在交配时将复射精管内的精子全部转移至雌蛾体内,不存在精子回流现象。  相似文献   

11.
中华绒螯蟹(Eriocheir sinensis)雄性生殖系统的组织学研究   总被引:16,自引:1,他引:15  
中华绒螯蟹雄性生殖系统的组织学研究表明:生精小管一侧为管壁上皮,另一侧为生发区,生殖细胞由生发区基底部同管腔增殖。输精管分为输精细管和贮精囊,管壁上皮具分泌功能,贮精囊有肌肉层。射精管壁肌肉层较厚,粘膜形成纵行皱襞。副性腺内壁为单层立方上皮。生殖系统发育有明显的季节性,8月开始发育加速,10月进入高峰,4月开始发育停滞。  相似文献   

12.
The effects of male-derived extracts on female receptivity were investigated in Callosobruchus maculatus (Coleoptera: Bruchidae). Injection of aqueous extracts of the male reproductive tract into the abdomen of females reduced receptivity. Aqueous extracts of male reproductive tracts were divided to three molecular weight (MW) fractions by ultrafiltration: Fractions: (I) MW<3 kDa, (II) 3-14 kDa, and (III)>14 kDa. Fraction II reduced female receptivity from 3h after injection, and Fraction III reduced female receptivity from 2 days after injection. On the other hand, no effect on receptivity was found for Fraction I. Furthermore, male reproductive tract organs were divided into accessory gland, testis, and seminal vesicle including the ejaculatory duct. Aqueous extracts of the seminal vesicle reduced receptivity of females immediately following injection, while aqueous extracts of the accessory gland reduced receptivity at the second day. The results suggest that the components of Fraction II existed in the seminal vesicle, and those of Fraction III in the accessory gland. The results of the present and the previous studies in Callosobruchus chinensis, a species closely related to C. maculatus, were compared and are discussed from the viewpoint of the significance of ejaculation in the two species.  相似文献   

13.
Variations in the adult male reproductive system among different groups of Hymenoptera offer characteristics that help studies on behavior and phylogenetics. The objective of this study was to describe the adult male reproductive system of three Trypoxylon (Trypargilum) species. For that, tissues were disseced, fixed in 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer, pH 7.2 and postfixed in 1% osmium tetroxide. The material was dehydratated and embedded for light and electron transmission microscopes. The species have similar reproductive systems, which are formed by a pair of testes, each one with three fusiforme follicles, from which emerges an efferent duct that later joins forming a deferent duct. The deferent duct opens into an ejaculatory duct. The first half of the deferent duct is enlarged and differentiated in a region specialized in sperm storage, the seminal vesicle. The accessory gland flows in the post-vesicular region of the deferent duct. The testes and vesicles are both covered with a conjunctive capsule. Sexually mature individuals have all spermatogenesis stages in their follicles. Sperms are released from testes in bundles which are disorganized inside seminal vesicles.  相似文献   

14.
钱静  沈和定  管菊 《动物学杂志》2015,50(4):600-606
雌雄同体贝类精子的储存和利用规律一直是国内外贝类生物学研究的难点之一,本文利用活体解剖、显微观察、组织切片和扫描电镜技术,综合研究了平疣桑椹石磺(Platevindex mortoni)的生殖系统及精子储存场所。结果显示,其生殖系统包括生殖器本部、雌性生殖部分和雄性生殖部分。生殖器本部由两性腺、两性输送管、蛋白腺、黏液腺、支囊组成;雌性生殖部分包括输卵管、受精囊、阴道,位于身体中后方体腔内;雄性生殖部分包括输精管、刺激器、阴茎、阴茎鞘和阴茎牵引肌,位于身体前端右侧体腔内;其阴茎有阴茎鞘,阴茎表面布满倒刺。平疣桑椹石磺阴茎为直线状,无雄性附属腺。未交配的性成熟个体支囊内充满细长精子,受精囊内无精子;而交配后充当雌性个体的支囊内均为细长的自体精子,受精囊内有大量活力较强的粗短精子,其支囊为自体精子的存储场所,而受精囊为异体精子的存储场所。其精子储运情况为:两性腺内精子成熟后暂存于支囊,交配时通过输精管运输至阴茎,由阴茎输送精子至对方的阴道,异体精子进入受精囊内存储待用。  相似文献   

15.
The fruit fly Drosophila melanogaster is an excellent model organism for studying insect reproductive biology. Although the gene expression profiles of both male and female reproductive organs have been studied in detail, their proteomic profiles and functional characteristics largely remained to be clarified. In this study, we conducted proteome mapping of the male internal reproductive organs using 2‐DE. We identified a total of 440 protein components from gels of the male reproductive organs (testis, seminal vesicle, accessory gland, ejaculatory duct, and ejaculatory bulb). A number of proteins associated with odorant/pheromone‐binding, lipid metabolism, proteolysis, and antioxidation were expressed tissue specifically in the male reproductive system. Based on our proteomic data set, we constructed reference proteome maps of the reproductive organs, which will provide valuable information toward a comprehensive understanding of Drosophila reproduction.  相似文献   

16.
17.
本研究主要采用透射电镜观察粉尘螨Dermatophagoides farinae (Hughes)生殖系统超微结构。粉尘螨雄性生殖系统是由精巢、 输 精管、 附腺、 射精管、 交配器官及附属交配器官组成。精巢内可同时有精子发育各阶段的细胞。精子无核膜、 核染色质聚集成束、 线 粒体缺乏典型的嵴、 胞质内有平行排列的电子致密薄片等为其特征性结构。雌性生殖系统由交合囊、 交合囊管、 储精囊、 囊导管、 卵 巢、 输卵管、 子宫及产卵管构成。卵巢内可见含多个细胞核的中央细胞, 其周为卵母细胞等生殖细胞。该研究丰富了对粉尘螨生殖系统 结构的认识。  相似文献   

18.
The male reproductive system of the fire ant, Solenopsis invicta Buren (Hymenoptera : Formicidae), consists of the testes, vasa efferentia, vasa deferentia, seminal vesicles, accessory glands, ejaculatory duct, wedge, aedeagal bladder, and external genitalia. The testes in newly eclosed males appear as 4 large white lobes filled with packets of sperm. Each lobe of the testes contains only one follicle. As the testes degenerate, the maturing sperm migrate through the vasa efferentia and vasa deferentia into the seminal vesicles. The seminal vesicles attach to the accessory glands, which are lined with secretory columnar epithelium. The posterior ends of the accessory glands taper and unite to form the ejaculatory duct. A sclerotized wedge is found at the junction of the accessory glands and the ejaculatory duct. An aedeagal bladder, joining the ejaculatory duct posterior to the wedge, is lined with squamous epithelium enveloped by heavy musculature. The ejaculatory duct continues posteriorly to form a distal aedeagus surrounded by 3 pairs of valves, comprising the external genitalia.  相似文献   

19.
David A. Doe 《Zoomorphology》1986,106(3):163-173
Summary The male reproductive system in Haplopharynx quadristimulus consists of paired testes, sperm ducts, seminal vesicles, seminal ducts, a copulatory organ containing prostatic vesicle and stylet apparatus, and the male canal. By electron microscopy all components appeared to be regional specializations of a canal extending from the testes to the body wall and lined by a multiciliated epithelium. The epithelium of the stylet apparatus contained six different cell types. One cell type (matrix syncytium) formed the stylet and the other five were located distal to the stylet/prostatic-vesicle junction along the male system epithelium. Each cell type was attached to the supporting intercellular matrix at a different level along the stylet apparatus. All cell types extended to the distal end of the stylet apparatus regardless of where they originated along its length. The cells in the apparatus lacked cilia, but one of the cell types contained rootlets. Modified rootlets or rootlet derivatives were possibly present in another cell type in the form of rootlet-like ribbons. The findings support the monophyly of the Macrostomida Haplopharyngida (by common occurrence of a matrix syncytium) and at the same time suggest their separation as two distinct taxa (by differences in the structure of the prostatic vesicle and other parts of the stylet apparatus).Abbreviations a accessory spine - c circular muscle - ce centriole - ci cilium - di dictyosome - e epithelial cell - ed ejaculatory duct - ep epidermal cell - f rootlet-like ribbon - g prostatic gland cell neck - g1 type I gland cell granules - g2 type II gland cell granules - g3 type III gland cell granules - h hemidesmosome - i intercellular matrix - im internal muscle - j septate junction - l stylet apparatus lumen - le spine lateral extension - lm longitudinal muscle - m matrix syncytium - mc male-canal epithelial cell - me male canal - mp male pore - mt microtubules - mv microvilli - n nucleus - nc nerve cell body - np nerve process - om oblique muscle - p prostatic vesicle epithelial cell - pv prostatic vesicle - r rootlet - s stylet - sa stylet apparatus - sc sensory receptor - sd sperm duct - se seminal duct - sl stylet lumen - sp spot desmosome - sr sperm - sv seminal vesicle - t terminal web - te testis - u ultrarhabdite - z zonula adhaerens - 2 cell type 2 - 3 cell type 3 - 4 cell type 4 - 6 cell type 6  相似文献   

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