In the present work, we analysed the male meiosis, the content and distribution of heterochromatin and the number and location of nucleolus organizing regions in Microtomus lunifer (Berg, 1900) by means of standard technique, C- and fluorescent bandings, and fluorescent in situ hybridization with an 18S rDNA probe. This species is the second one cytogenetically analysed within the Hammacerinae. Its male diploid chromosome number is 31 (2n=28+X1X2Y), including a minute pair of m-chromosomes. The diploid autosomal number and the presence of m-chromosomes are similar to those reported in Microtomus conspicillaris (Drury, 1782) (2n=28+XY). However, Microtomus lunifer has a multiple sex chromosome system X1X2Y (male) that could have originated by fragmentation of the ancestral X chromosome. Taking into account that Microtomus conspicillaris and Microtomus lunifer are the only two species within Reduviidae that possess m-chromosomes, the presence of this pair could be a synapomorphy for the species of this genus. C- and fluorescent bandings showed that the amount of heterochromatin in Microtomus lunifer was small, and only a small CMA3 bright band was observed in the largest autosomal pair at one terminal region. FISH with the 18S rDNA probe demonstrated that ribosomal genes were terminally placed on the largest autosomal pair. Our present results led us to propose that the location of rDNA genes could be associated with variants of the sex chromosome systems in relation with a kind of the sex chromosome systems within this family. Furthermore, the terminal location of NOR in the largest autosomal pair allowed us to use it as a chromosome marker and, thus, to infer that the kinetic activity of both ends is not a random process, and there is an inversion of this activity.

The Cimicidae (Hemiptera) are known to be blood ectoparasites primarily on birds and bats. Three species of the subfamily Haematosiphoninae are known from Argentina: Acanthocrios furnarii, Ornithocoris toledoi, and Psitticimex uritui; all feed on diverse avian hosts. The chromosome number and male meiosis of A. furnarii, and P. uritui from new Argentinean samples are analyzed and compared with previous data. The sample of A. furnarii described by Ueshima (1966) with 2n = 32 + XY (male), strikingly differs from the present results (2n = 10 + XY, male). The diploid number of P. uritui agree with the previously reported by Ueshima (1966), 2n = 28 + X 1 X 2 Y (male). Taxonomical implications about the identity of A. furnarii are discussed and the mechanisms of the karyotype evolution of species belonging to Haematosiphoninae are proposed.

In this study, we analysed a population of Zelurus femoralis longispinis polymorphic for chromosomal number. The fundamental karyotype of this subspecies is 2n = 22 = 20A + XY (male), but individuals with 2n = 23 = 20A + XY + extra chromosome have been found at high frequency and collected at different time periods. We examined male meiotic behaviour, average length as percentage of the sex chromosomes, the content, distribution and composition of heterochromatin, and the number and location of ribosomal DNA in the two cytotypes found. The meiotic behaviour of the extra chromosome was highly regular and similar to that of sex chromosomes. The average length of the sex chromosomes in individuals not carrying the extra chromosome was significantly greater than in those carrying it. The results support a hypothesis that the extra chromosome might have originated by fragmentation of the original X chromosome into two unequal‐sized chromosomes (X1 and X2), leading to an X1X2Y multiple system. Maintenance of the polymorphism with time appears to indicate that the new chromosomal variant is neutral or at least not detrimental, or that it could be selectively advantageous. This polymorphic population represents direct evidence of a multiple sex chromosome system originating through fragmentation of a single X in Reduviidae as well as in Heteroptera. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2013, 110, 757–764.

Members of the family Cimicidae (Heteroptera: Cimicomorpha) are temporary bloodsuckers on birds and bats as primary hosts and humans as secondary hosts. Acanthocrios furnarii (2n=12=10+XY, male) and Psitticimex uritui (2n=31=28+X1X2Y, male) are two monotypic genera of the subfamily Haematosiphoninae, which have achiasmatic male meiosis of collochore type. Here, we examined chromatin organization and constitution of cimicid holokinetic chromosomes by determining the amount, composition and distribution of constitutive heterochromatin, and number and location of nucleolus organizer regions (NORs) in both species. Results showed that these two bloodsucker bugs possess high heterochromatin content and have an achiasmatic male meiosis, in which three regions can be differentiated in each autosomal bivalent: (i) terminal heterochromatic regions in repulsion; (ii) a central region, where the homologous chromosomes are located parallel but without contact between them; and (iii) small areas within the central region, where collochores are detected. Acanthocrios furnarii presented a single NOR on an autosomal pair, whereas P. uritui presented two NORs, one on an autosomal pair and the other on a sex chromosome. All NORs were found to be associated with CMA3 bright bands, indicating that the whole rDNA repeating unit is rich in G+C base pairs. Based on the variations in the diploid autosomal number, the presence of simple and multiple sex chromosome systems, and the number and location of 18S rDNA loci in the two Cimicidae species studied, we might infer that rDNA clusters and genome are highly dynamic among the representatives of this family.