To the nomenclature of two species of the genus Adomerus (Heteroptera: Cydnidae).

The study of the lectotype of Sehirus fuscipennis Horváth, 1899 showed that this specimen is conspecific with Canthophorus maculipes sensu Aukema Constant, 2016 and Adomerus maculipes sensu Gapon, 2018. To promote stability of nomenclature, the neotype of Cydnus maculipes Mulsant et Rey 1852 is designated instead of the lost syntypes. The name Sehirus aeneus Walker, 1867 is placed in synonymy with Adomerus maculipes (Mulsant et Rey, 1852). The name Adomerus fuscipennis (Horváth, 1899), stat. resurr. is reinstated. Colouration of the hemelytra, the structure of the parameres and aedeagi of the holotype of S. aeneus Walker, 1867 (female), of a male of A. maculipes, being topotypic with the latter, and of the lectotype of S. fuscipennis Horváth, 1899 are compared with each other and with descriptions of the terminalia of both species, recently published by the second author based on material from different localities. A map of the distribution of both species is given according to the literature data and studied collection materials.

A new species of the genus Rhaphidosoma Amyot et Serville, 1843 (Heteroptera, Reduviidae), with data on its chromosome complement.

A new species, Rhaphidosomapaganicum sp. nov. (Heteroptera: Reduviidae: Harpactorinae: Rhaphidosomatini), is described from the Dry Zone of Myanmar. It is the fifth species of Rhaphidosoma Amyot et Serville, 1843, known from the Oriental Region, and the first record of the genus for Myanmar and Indochina. The structure of the external and internal terminalia of the male and female is described and illustrated in detail. The completely inflated endosoma is described for the first time in reduviids. The complex structure of the ductus seminis is shown; it terminates with a voluminous seminal chamber which opens with a wide secondary gonopore and may be a place where spermatophores are formed. The new species is compared with all congeners from the Oriental Region and Western Asia. It is characterised by the absence of distinct tubercles on the abdominal tergites of the male, the presence only two long tubercles and small rounded ones on the abdominal tergites VII and VI, respectively, in the female, the presence of short fore wing vestiges which are completely hidden under longer fore wing vestiges, and other characters. In addition to the morphological description, an account is given of the male karyotype and the structure of testes of Rh.paganicum sp. nov. and another species of Harpactorinae, Polididusarmatissimus Stål, 1859 (tribe Harpactorini). It was found that Rh.paganicum sp. nov. has a karyotype comprising 12 pairs of autosomes and a multiple sex chromosome system (2n♂=24A+X1X2X3Y), whereas P.armatissimus has a karyotype comprising five pairs of autosomes and a simple sex chromosome system (2n♂=10A+XY). The males of these species were found to have seven and nine follicles per testis, respectively. FISH mapping of 18S ribosomal DNA (major rDNA) revealed hybridisation signals on two of the four sex chromosomes (Y and one of the Xs) in Rh.paganicum sp. nov. and on the largest pair of autosomes in P.armatissimus. The presence of the canonical "insect" (TTAGG) n telomeric repeat was detected in the chromosomes of both species. This is the first application of FISH in the tribe Raphidosomatini and in the genus Polididus Stål, 1858.