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.

C-banding was carried out on Belostoma elegans (2n = 26 + X1X2Y ) (o'), B. micantulum (2n = 14 + XY) (~) and B. oxyurum (2n = 6 + XY) (o') (Belostomatidae, Heteroptera). The C-bands always have a telomeric localization and no interstitial bands were detected. An inverse relationship between chromosome size and chromosome number exists, and besides, an inverse relationship between chromosome size and the size of the Cbands was observed. The DNA content was determined in all three species. B. elegans has a C content of 1.55 + 0.06 pg, B. micantulum has 0.88 + 0.04 pg and B. oxyurum had 0.53 + 0.04 pg.Considering the male meiotic characteristics, the chromosome complement and the results of C-banding and DNA content, the karyotype of B. oxyurum probably originated through autosomal fusions. The karyotype of B. micantulum and B. elegans could have originated through autosomal fusions or fragmentations respectively; with the information available up to now it is not possible to discard any of the two pathways.

The amount, composition and location of heterochromatin in Athaumastus haematicus (Stål, 1859), Leptoglossus impictus (Stål, 1859), Phthia picta (Drury, 1770) (Coreidae), Largus rufipennis Laporte, 1832 (Largidae) and Jadera sanguinolenta (Fabricius, 1775) (Rhopalidae) are analyzed by C-banding and DAPI/ CMA fluorescent banding. As the rule for Heteroptera the possession of holokinetic chromosomes and a pre-reductional type of meiosis cytogenetically characterize these five species. Besides, all of them (except L. rufipennis) present a pair of m chromosomes. C-banding technique reveals the absence of constitutive heterochromatin in A. haematicus, scarce C-positive blocks in L. impictus and J. sanguinolenta, and C-positive heterochromatin terminally located in P. picta and L. rufipennis. All C-bands are DAPI bright, except for a DAPI dull/CMA bright band at one telomeric end of the X chromosome in L. rufipennis, which probably corresponds to a nucleolar organizing region. The results of the banding techniques are analyzed in relation to the chiasma frequency and distribution in the five species, and it is concluded that there should exist some constraints to the acquisition and/ or accumulation of heterochromatin in their karyotypes.