Abstract. Species of Pentatomidae are cytogenetically characterized by the presence of holokinetic chromosomes, a pre-reductional type of meiosis, and a great constancy not only in chromosome number (2n = 14 in 85% of the 250 species analyzed) but also in the sex chromosome determining system (XY/XX).Edessa meditabunda and E. rufomarginata males have 2n=14=12 + XY, and both species present small telomeric positively heteropycnotic bands which are DAPI and CMA bright. In E. meditabunda the NOR region is clearly revealed at the telomeric region of the largest autosomal pair by silver staining and CMA banding. Meiotic behaviour of both species follows the general pat tern of the order: autosomes divide pre-reductionally, sex chromosomes are achiasmatic and divide postreductionally, and at both metaphase plates the autosomes become arranged in a circle with the sex chromosomes lying at its center. In E. meditabunda, how ever, the larger sex chromosome is generally observed at metaphase I forming part of the ring of autosomal bivalents. Bivalents with two chiasmata are frequently observed in E. meditabunda and E. rufomarginata', mean chiasma frequency (6.45 and 6.26, respec tively) differ significantly between both species, but differences between populations within each species are not significant.The metaphase plate arrangement of autosomes and sex chromosomes is rather constant in Heteroptera. However, our results in E. meditabunda together with previous reports in other species of the order led us to suggest that the metaphase plate arrangement is more liable to variation at the first meiotic division than at the second one, when it is almost constant. The presence of ring bivalents in both species here analyzed constitutes further evidence against the previous statement of only one chiasma per bivalent in Heteroptera.

The suborder Heteroptera constitutes one of the most important insect groups because most species are plants feeders and cause damage on many plants of economic importance. One of the most important cytogenetic characteristics of Heteroptera is the holokinetic nature of the chromosomes. One particular feature of some species of Pentatomidae is the regular presence of an abnormal meiosis in one testicular lobe (harlequin lobe). From the 28 species cytogenetically analysed from Argentine material, 21 present the diploid number 2n ¼ 14, four species present a reduced number (2n ¼ 12) and another three species possess an increased diploid number (2n ¼ 16); among all these only three present an harlequin lobe. In the present work, a bibliographic review of the chromosome number and sex determining system of 294 species and subspecies belonging to 121 genera within the subfamilies Asopinae, Discocephalinae, Edessinae, Pentatominae, Phyllocephalinae and Podopinae is presented. The male diploid numbers range from six to 27 with a mode in 14 chromosomes; this last diploid number is present in 85% of the species. The sex chromosome determining system is XY/XX except in three species: Macropygium reticulare (Fabricius, 1803), Rhytidolomia senilis (Say, 1832) and Thyanta calceata (Say, 1832) which present derived sex chromosome systems. Furthermore, the cytogenetic relationships with the other families of Pentatomoidea are discussed.

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Acledra comprises 15 taxonomically identified species, most of which are crop pests. This is the first cytogenetic study of species of this genus. Acledra kinbergii and A. modesta showed the modal number of the Pentatomidae (2n = 14 = 12 + XY), while A. bonariensis had a reduced complement (2n = 12 = 10 + XY), with a markedly larger autosomal pair. Meiotic behavior follows the general pattern of the family; the autosomes divide pre-reductionally, the sex chromosomes are achiasmatic and divide post-reductionally, and at metaphase II the autosomes show a ring-shaped configuration with the pseudobivalent at the center. However, the configuration at metaphase I varies; A. modesta shows the typical arrangement (ring of bivalents with the sex chromosomes lying at its center). In A. kinbergii, the sex chromosomes are part of the ring or only the Y chromosome is at the center. In A. bonariensis, the ring arrangement is not well defined. There are also differences at the diffuse stage; chromatin strands of different width are observed in A. bonariensis and A. modesta, whereas bivalents do not entirely lose their identity in A. kinbergii. In A. bonariensis, the reduced complement may have originated from the fusion of the two larger non-homologous autosomes, which could characterize the ancestral karyotype of this genus. The presence of secondary constrictions in the larger pair of A. modesta and A. bonariensis may support this hypothesis. Since secondary constrictions are uncommon in the holokinetic chromosomes of heteropterans, their presence in these species may indicate that it is a plesiomorphic character of the genus.

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Abstract. In Mormidea paupercula (n = 6 + XY in males), the presence of a CMA3-bright band in the telomeric regions on both sex chromosomes allowed the analysis of the kinetic activity of the sex univalents and XY pseudobivalent at the first and second meiotic divisions, respectively. The separation of the sister chromatids of the sex chromosomes occurs from a pair of telomeric regions (with or without a band), with opposite telomeric regions remaining associated with each other at meiosis I; the behaviour of both sex chromosomes differs, on the X chromosome both telomeric regions are similarly active, while on the Y chromosome the telomeric region without a band is more frequently active. At the second division, the most frequent associations in the pseudobivalent occur between the telomeric regions of both sex chromosomes with bands or without bands. Therefore, in both meiotic divisions, the same telomeric region on the sex chromosomes could lead the migration, in contrast to that observed usually in autosomal bivalents. These results provide evidence that the sex chromosomes of Heteroptera show more than one pattern of attachment to the spindle.