a1_There are few studies on the morphology and meiosis in the testicles of Heteroptera, but are extremely important, especially for the family Pentatomidae, because in some species in this family meiosis in the testicular lobes results in the production of non-fertile spermatozoa. With the aim of improving the level of understanding of this phenomenon the morphology of the testes and spermatogenesis in 10 species of Pentatomidae were recorded and compared. All of them have testes covered by a pigmented peritoneal sheath. In some species the internal membrane or just inside the peritoneal sheath is pigmented. The pigmentation of both membranes varied. The pigmentation of both was either yellow, or the internal membrane was yellowish and the external one reddish. When the membrane is pigmented, the colour is red or yellow. The number of lobes varied from 3 to 7, with intermediate numbers of 4 and 6. The size and diameter of the lobes are similar in all the species studied, except Proxys albopunculatus, in which the diameter of the third and fifth is smaller than that of the other lobes. The behaviour of the cells during spermatogenesis was the same in all lobes of most species, except in P. albopunctulatus, in which the harlequin lobe is absent and the cells in lobes 4 and 6 exhibited characteristics different from those of cells in lobes 1-3 and 5. Chlorocoris complanatus and Loxa deducta (both Pentatominae) have a harlequin lobe (lobe 5). The chromosome complements recorded were: 2n = 12 (10A + XY) in Dichelops melacanthus and Edessa collaris, 2n = 14 (12A + XY) in C. complanatus, Edessa meditabunda, Ladeaschistus sp., Loxa deducta, P. albopunctulatus, Piezodorus guildinii and Thyanta perditor and 2n = 16 (14A + XY) in Edessa affinis. Thus, this study extends the knowledge of characteristics, such as the pigmentation of the peritoneal sheath, number of testicular lobes, the occurrence of meiotic cells in some, a2_testicular lobes, and the chromosome complements of the family Pentatomidae., and Hederson Vinícius De Souza, Aline Sumitani Murakami, Juliana De Moura, Elisângela Cristiane De Almeida, Inaiá Fernandes Gallego Marques, Mary Massumi Itoyama.
Facultative diapause in the wax moth, Galleria mellonella, occurs in the final larval instar. Application of juvenile hormone analogs (JHAs) to the larvae of this species has similar effects to diapause, in terms of prolonged development of the larval stages and the arrest in the metamorphosis of internal organs. Here, we focus on testes development and spermatogenesis at the end of larval development in G. mellonella, how they are affected by diapause induced by an environmental decrease in temperature to 18°C and the application of a JHA (fenoxycarb) to larvae. Because neither testis development nor spermatogenesis are described in detail for this species, we examined them in individuals not in diapause during the period from the last larval instar to the newly emerged adult and present a timetable of changes that occur in the development of testes in this species. These observations have increased the very limited data on the course of spermatogenesis in pyralid insects. We then used these data for comparative analysis of testes in larvae from two experimental groups: individuals in diapause and those treated with fenoxycarb. The results on the general morphology testes revealed obvious degenerative changes caused by fenoxycarb (but not by diapause), including testicular wall hypertrophy and disarrangement of testicular follicles. Moreover, treatment with fenoxycarb finally resulted in the disintegration of nearly all testicular cyst-containing germ cells at different stages of spermatogenesis, a situation never previously described in the literature. In contrast, the main effect of diapause on testes was merely the degeneration of spermatocytes in the proximal regions of the testicular follicles. Finally, the TUNEL analyses, revealed that the degenerative changes in germ cells were apoptotic in character in the testes of both individuals in diapause and fenoxycarb-treated males., Piotr Bebas, Bronislaw Cymborowski, Michalina Kazek, Marta Anna Polanska., and Obsahuje bibliografii
We examined effects of seasonality, larval food availability and larval rearing density on sperm length, sperm transfer rates and body size in the bivoltine scorpionfly Panorpa vulgaris. Males of the first annual generation were larger and had larger sperm. Comparing individuals of two summer generations showed that adult males resulting from group bred, ad libitum fed larvae were larger but had smaller sperm than males resulting from singly kept, food deprived larvae. Thus, sperm size is not a simple function of body size. Instead, we suggest that sperm size modification was caused by varying rearing densities. Group bred individuals produced smaller sperm but transferred at higher rate. This indicates a trade-off between sperm number and sperm size as predicted by evolutionary models of sperm production. Given the strong influence of larval history in our present work, we recommend that future studies investigating the consequences of varying sperm competition risk or intensity on male gametic strategies should also control for larval history in order to avoid distorting effects.
Ultrastructural analysis revealed that the spermatozoon of Discocotyle sagittata (Leuckart, 1842) is composed of two parallel axonemes, mitochondrion, nucleus and cortical microtubules. The nucleus, which occupies a central/distal position and has an unusual crescent-shaped profile, is slightly shorter than the mitochondrial rod. The two axonemes, which are of unequal length, and the cortical microtubules (up to 68 forming a continuous ring in the principal region) extend almost the entire length of the spermatozoon. A fold of the plasma membrane creates a unilateral flange or undulating membrane. Epifluorescence microscopy indicated that spermatogenesis gives rise to clusters of 64 spermatids connected to a common cytophore. Spermiogenesis and the structure of the filiform sperm of D. sagittata conform to the typical polyopisthocotylean pattern.