Fine structure of the spermatheca and of the accessory glands in Orchesella villosa (Collembola, Hexapoda)

The spermatheca and the accessory glands of the collembolan Orchesella villosa are described for the first time. Both organs exhibit ultrastructural differences, according to the time of the intermolt in which the specimens were observed. A thick cuticular layer lines the epithelial cells of the accessory glands. In the reproductive phase, they are involved in secretory activity; a moderately dense secretion found in the apical cell region opens into the gland lumen. Cells with an extracellular cistern are intermingled with the secretory cells. These cells could be involved in fluid secretion, with the secretory product opening into the cistern which is filled with an electron-transparent material. After the reproductive phase, the gland lumen becomes filled with a dense secretion. The accessory gland secretion may play a protective role towards the eggs. The spermatheca is located between the accessory glands; its epithelium is lined by a thin cuticle forming spine-like projections into the lumen and consists of cells provided with an extracellular cistern. Secretory cells, similar to those seen in the accessory glands, are missing. Cells with a cistern could be involved in the production of a fluid secretion determining sperm unrolling and sperm motility.     

Effects of sublethal doses of chlorfluazuron on insemination and number of inseminated sperm in the common cutworm, Spodoptera litura (F.) (Lepidoptera: Noctuidae)

Sublethal doses (LD₁₀: 1.00 ng larva^?1; or LD₃₀: 3.75 ng larva^?1) of chlorfluazuron were applied topically to the cuticles of newly moulted fifth instars of the common cutworm, Spodoptera litura (F.) (Lepidoptera, Noctuidae). During mating, the treated males transferred spermatophores of a significantly lower weight into females. The weight of spermatophores transferred by LD₃₀‐treated males was significantly lower than the weight of spermatophores transferred by LD₁₀‐treated males, which was in turn significantly lower than the weight of spermatophores transferred by untreated males. The transfer of spermatophores was delayed by 5–15 min in LD₁₀‐ and LD₃₀‐treated males. However, mating duration was not affected by chlorfluazuron treatment. The transfer of spermatozoa was also delayed by 5–10 min in LD₁₀‐ and LD₃₀‐treated females. Polygynous male adults mated an average of ten times during their lifespan of 11–13 days when paired every day with a new virgin female of the same age. The number of matings per polygynous male was not affected by chlorfluazuron treatment, but the first mating was delayed by 1 day. The number of inseminated sperm found in the spermatophore averaged 10.3 (± 2.1) × 10⁵ over the lifespan of a male, in which the number of eupyrene sperm was 5.4 (± 1.1) × 10⁵. The number of inseminated eupyrene sperm decreased by 66% and 88%, respectively, in LD₁₀‐ and LD₃₀‐treated males. No significant reduction in the number of inseminated eupyrene sperm was observed when females were treated with LD₁₀ or LD₃₀ doses, nor was there a significant reduction when both sexes were treated with the LD₁₀ or LD₃₀ doses relative to treatment of males with the same doses. The ratio of inseminated eupyrene to apyrene sperm was not affected by chlorfluazuron treatment.     

Age at sexual maturity of male and female banana weevils,Cosmopolites sordidus Germar (Coleoptera: Curculionidae)

This study was to determine the age at sexual maturity and the relationships between age and internal reproductive organs of Cosmopolites sordidus. Male banana weevils become sexually mature 18 days after emergence (DAE), that is after 2 weeks of adult eclosion, in spite of the fact that spermatogenesis is completed at emergence. A positive correlation exists between age and male internal organs, for example for mean testis diameter (r = .849, p ≤ .001), mean seminal vesicle diameter (r = .679, p ≤ .001), mean accessory gland length (r = .561, p ≤ .01) and mean accessory gland diameter (r = .498, p ≤ .05), respectively. Significant differences were recorded between sexually mature and immature weevils with respect to mean testis diameter (T = 4.471, p ≤ .001) and mean seminal vesicle diameter (T = 3.939, p ≤ .001), but not with mean accessory gland length and mean accessory gland diameter (T = 1.899 and 1.661). Male internal organs were visibly underdeveloped at emergence but became significantly enlarged and developed on attainment of sexual maturity. Female C. sordidus, on the other hand, are sexually mature at 5 DAE. There was also a strong, positive correlation between age of females and mean ovariole length (r = .656, p ≤ .001), and significant differences existed between mean ovariole lengths of sexually mature and immature females (T = 4.306, p ≤ .001). Increasing age of females witnessed progressive increases in ovariole lengths and developmental changes within female ovarioles and calyces. The findings made here may be helpful in Musa germplasm screening works, as weevils bred on susceptible cultivars may reveal similar results, while those bred on resistant ones may experience possible delays in their reproductive developments.     

Morphology of the female reproductive system of European pea crabs (Crustacea,Decapoda, Brachyura,Pinnotheridae)

Commensal pea crabs inhabiting bivalves have a high reproductive output due to the extension andfecundity of the ovary. We studied the underlying morphology of the female reproductive system in the Pinnotheridae Pinnotheres pisum, Pinnotheres pectunculi and Nepinnotheres pinnotheres using light microscopy and transmission electron microscopy (TEM). Eubrachyura have internal fertilization: the paired vaginas enlarge into storage structures, the spermathecae, which are connected to the ovaries by oviducts. Sperm is stored inside the spermathecae until the oocytes are mature. The oocytes are transported by oviducts into the spermathecae where fertilization takes place. In the investigated pinnotherids, the vagina is of the “concave pattern” (sensu Hartnoll 1968 ): musculature is attached alongside flexible parts of the vagina wall that controls the dimension of its lumen. The genital opening is closed by a muscular mobile operculum. The spermatheca can be divided into two distinct regions by function and morphology. The ventral part includes the connection with vagina and oviduct and is regarded as the zone where fertilization takes place. It is lined with cuticle except where the oviduct enters the spermatheca by the “holocrine transfer tissue.” At ovulation, the oocytes have to pass through this multilayered glandular epithelium performing holocrine secretion. The dorsal part of the spermatheca is considered as the main sperm storage area. It is lined by a highly secretory apocrine glandular epithelium. Thus, two different forms of secretion occur in the spermathecae of pinnotherids. The definite role of secretion in sperm storage and fertilization is not yet resolved, but it is notable that structure and function of spermathecal secretion are more complex in pinnotherids, and probably more efficient, than in other brachyuran crabs. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.     

Morphology and function of the female reproductive system of Ebalia tumefacta (Decapoda,Brachyura, Leucosiidae)

In this article, the morphology and function of the female reproductive organs of Ebalia tumefacta were investigated using histological methods. While the vagina conforms to the concave type, the study reveals a new orientation of seminal receptacle compartments. The seminal receptacle consists of two chambers, which are oriented in anterior‐posterior direction. This is in contrast to the dorso‐ventral orientation of seminal receptacle chambers in all other known brachyuran crabs. The anterior chamber is lined by cuticle, whereas the posterior chamber is covered with a holocrine glandular epithelium. The oviduct connection is located ventrally, close to the opening of the vagina. The oviduct orifice is characterized by a transition of the epithelium lining of the oviduct to the seminal receptacle holocrine glandular epithelium. Special features are muscle fibers, which are attached to the oviduct orifice and to the sternal cuticle as well. The muscle fibers can be found exactly at that point where the oviduct opens into the seminal receptacle and are secondly attached to the sternum beneath. This musculature is newly described for Eubrachyuran crabs. This musculature can be interpreted as an important feature in the fertilization and egg‐laying process in relation to supporting and controling the inflow of eggs into the seminal receptacle lumen. These new discoveries were compared to the known pattern of an Eubrachyuran seminal receptacle. J. Morphol. 276:517–525, 2015. © 2014 Wiley Periodicals, Inc.     

Inclusion of rare taxa from Blattidae and Anaplectidae improves phylogenetic resolution in the cockroach superfamily Blattoidea

Cockroaches are an ecologically and economically important insect group, but some fundamental aspects of their evolutionary history remain unresolved. In particular, there are outstanding questions about some of the deeper relationships among cockroach families. As a group transferred from Blaberoidea Saussure to Blattoidea Latreille, the evolutionary history of the family Anaplectidae Walker requires re-evaluation. In our study, we infer the phylogeny of Blattoidea based on the mitochondrial genomes of 28 outgroup taxa and 67 ingroup taxa, including 25 newly sequenced blattoid species mainly from the families Anaplectidae and Blattidae Latreille. Our results indicate that Blattoidea is the sister group of the remaining Blattodea Brunner von Wattenwyl and that Blattoidea can be divided into three main clades: Blattidae + Tryonicidae McKittrick & Mackerras, Lamproblattidae McKittrick + Anaplectidae and Termitoidae Latreille + Cryptocercidae Handlirsch. Our analyses provide robust support for previously uncertain hypotheses. The sister group of Termitoidae + Cryptocercidae (Xylophagodea Engel) is inferred to constitute the rest of Blattoidea, for the first time. Within Blattidae, Hebardina Bey-Bienko is placed as the sister lineage to the rest of Blattidae. The subfamily Archiblattinae is polyphyletic, Blattinae is paraphyletic and Polyzosteriinae is monophyletic (Macrocercinae Roth not included); the genus Periplaneta Burmrister is polyphyletic. Based on the results of our phylogenetic analyses, we have revised these taxa. A new subfamily, Hebardininae subfam.nov. , is proposed in Blattidae. Archiblattinae and Shelfordella Adelung are synonymized with Blattinae and Periplaneta, respectively: Archiblattinae Kirby syn.nov. and Shelfordella Adelung syn.nov. Our inferred divergence times indicate that Blattoidea emerged in the Late Triassic, with six families in Blattoidea diverging in the Middle and Late Jurassic. We suggest that the divergences among lineages of Asian Blattidae and Anaplectidae were driven by the uplift of the Himalayas and deglaciation during the Quaternary, leading to the present-day distributions of these taxa.     

Physiological basis for sterilizing effects of constant light in Lymantria dispar

ABSTRACT Females of gypsy moth, Lymantria dispar L. (Lepidoptera: Lymantriidae), mated to males kept in constant light (LL) as pharate adults fail to oviposit. In males, a rhythm of sperm release from the testis that occurs in light-dark (LD) cycles is abolished in LL, and the total amount of sperm released from the testis is approximately half of that of LD males. Moreover, any sperm that may be released from the testis of LL males tend to remain in the vasa deferentia instead of moving into the duplex as in LD males. Consequently, in LL very few sperm bundles are transferred to the bursa copulatrix during mating; furthermore, these bundles fail to disperse into spermatozoa and sperm do not reach the spermatheca. The presence of a spermatheca filled with sperm must play an important role in controlling oviposition because their removal from mated females prevents egg-laying. Our results indicate that the rhythm of sperm release from the testis is essential for the ability of sperm to migrate in male and female reproductive tracts. The rhythms may help to synchronize final stages of sperm development with the activity of phagocytic and secretory cells lining the reproductive tract.     

The effect of mating on phonotactic behaviour in Gryllus bimaculatus (De Geer)

Abstract. Phonotaxis of G. bimaculatus females is expressed by a course-consistent, directional approach to a conspecific model calling song emitted alternatingly at sound intensities of 50–90 dB SPL and appears at the age of 6–7 days, the onset of maturation. Mating abolishes phonotaxis after about 1 h. By that time, the content of the attached spermatophore has migrated into the female's sper-matheca. Removal or emptying of the spermatheca, or severing the ventral nerve cord, fully reinstates phonotaxis, whereas ovariectomy has no effect. We suggest that mechanoreceptors record the expansion of the filled spermatheca and that the inhibitory message is communicated via the ventral nerve cord anteriorly to an unknown control centre in the brain. The loss of phonotaxis is combined with reduced locomotor activity and results in the female no longer being attracted to another calling male.