Marchini Daniela, Del Bene Giovanna, Dallai Romano
Dipartimento di Biologia Evolutiva, Università degli Studi di Siena, Via A. Moro 2, Siena, Italy.
J Morphol. 2010 Apr;271(4):473-82. doi: 10.1002/jmor.10811.
At mating, female insects generally receive and store sperm in specific organs of their reproductive tract called spermathecae. Some Heteroptera, such as Cimicomorpha, lack a true spermatheca; some have receptacles of novel formation where sperm cells can transit or be stored. In Tingidae, there are two sac-like diverticula, the "pseudospermathecae," each at the base of a lateral oviduct, which previously were considered to function as spermathecae. However, this role has never been documented, either by ultrastructural studies or by observations of sperm transit in the female reproductive tract. In this article, we investigate the morphology and the ultrastructure of the female reproductive apparatus in the economically important tingid species Stephanitis pyrioides, focusing our attention on the functional role of the pseudospermathecae in an evolutionary perspective. Each ovary consists of seven telotrophic meroistic ovarioles, the long pedicels of which enlarge into a bulb-like structure near the terminal oocyte. The ovarioles flow into two long lateral oviducts, which join to form a very short common oviduct. Basally, each lateral oviduct is connected through a short duct to one of two pseudospermathecae. The ultrastructure of the ectodermal epithelium of the pseudospermathecae is dramatically different in sexually immature or mated females. In virgin females, cells delimit a very irregular lumen, filled with a moderately electron-dense granular material. The large nucleus adapts to their irregular shape, which can have long projections in some regions and be flattened in others. After mating, epithelial cells generally elongate and display an apical layer of microvilli extending beneath the cuticle, often containing mitochondria. In the lumen of the pseudospermathecae there is a dense brownish secretion. No sperm cells were ever found inside this organ. After mating, sperm move upward along the lateral oviducts and the ovarioles, accumulating in the bulb-like structure of the pedicels, and proceeding into the distal region between the follicle cells surrounding the oocyte and the ovariole wall. The egg, most likely fertilized in the bulb-like region of the ovariole, moves through the lateral oviduct, entirely enters the pseudospermatheca and is smeared with its secretion just before oviposition. We exclude a function of sperm storage for the pseudospermathecae, and instead suggest a novel role for these organs as reproductive accessory glands.
在交配时,雌性昆虫通常会在其生殖道的特定器官(称为受精囊)中接收并储存精子。一些半翅目昆虫,如臭虫亚目,没有真正的受精囊;有些有新形成的储存器,精子细胞可以在其中运输或储存。在网蝽科中,有两个囊状憩室,即“假受精囊”,分别位于侧输卵管的基部,以前被认为起到受精囊的作用。然而,无论是通过超微结构研究还是对雌性生殖道中精子运输的观察,都从未证实过这一作用。在本文中,我们研究了具有经济重要性的网蝽物种梨冠网蝽雌性生殖器官的形态和超微结构,从进化的角度重点关注假受精囊的功能作用。每个卵巢由七个端滋式多滋卵巢小管组成,其长柄在终端卵母细胞附近膨大形成球状结构。卵巢小管汇入两条长的侧输卵管,两条侧输卵管汇合形成一条非常短的共同输卵管。在基部,每条侧输卵管通过一条短导管与两个假受精囊之一相连。在未成熟或已交配的雌性中,假受精囊的外胚层上皮超微结构有显著差异。在未交配的雌性中,细胞界定出一个非常不规则的管腔,充满中等电子密度的颗粒物质。大细胞核适应其不规则形状,在某些区域可能有长突起,在其他区域则扁平。交配后,上皮细胞通常会伸长,并显示出一层顶端微绒毛延伸至角质层下方,微绒毛中常含有线粒体。在假受精囊的管腔中有浓稠的褐色分泌物。在这个器官内从未发现过精子细胞。交配后,精子沿着侧输卵管和卵巢小管向上移动,聚集在柄的球状结构中,并进入围绕卵母细胞的滤泡细胞和卵巢小管壁之间的远端区域。卵子很可能在卵巢小管的球状区域受精,然后通过侧输卵管移动,完全进入假受精囊,并在产卵前被其分泌物涂抹。我们排除假受精囊具有储存精子的功能,而是认为这些器官作为生殖附属腺具有新的作用。