Members of the clade Trichophora (Hemiptera: Heteroptera: Pentatomomorpha) have trichobothria on their abdominal sterna. There is no comparative study of the fine structure of abdominal trichobothria in the group and until now the trichobothria of their immatures were virtually unknown. The fine structure of the abdominal trichobothrial complex (= the trichobothrium and its associated structures) of adults of 98 species belonging to 25 families in 5 superfamilies and larvae of 7 species belonging to 7 families in 2 superfamilies of Trichophora were examined using scanning electron microscopy. This study indicates that the fine structure of the abdominal trichobothria is very variable and useful for determining evolutionary lineages within the clade. Six types of bothria, three of trichomes and three of microtrichia are recognized and their evolutionary transformations discussed. Changes in the size of trichomes, and density and size of the microtrichia during the postembryonic development of selected species are discussed.
† Pyrenicocephalus jarzembowskii, gen. et sp. n. (Hemiptera: Heteroptera: Enicocephalomorpha: Enicocephalidae: Enicocephalinae) from Early Eocene, London Clay, England, Isle of Sheppey, is described and illustrated according to the unique pyritized adult head reported as a larval enicocephalid head by Jarzembowski (1986). The head anatomy of similar and related genera of Enicocephalinae is compared and the close relationship of the new genus to a clade including the extant genera Oncylocotis, Embolorrhinus and Hoplitocoris is suggested, most probably as the sister genus to Hoplitocoris (presently with Afrotropical, East Palaearctic and Oriental range).
Blaena tamasi sp. n., the first species of Cydnidae with staphylinoid modification of wings, is described from Western Australia. The rare cases of wing modifications in Cydnidae and Pentatomoidea are briefly discussed. A key to all known species of the genus Blaena Walker is also provided.
The reservoirs of dorso-abdominal scent glands and the occurrence of the metapleural scent gland evaporatoria in the adults of nine central European and one North American species in the family Rhopalidae (Hemiptera) were studied. All published data about the persistence of the dorso-abdominal scent glands in rhopalid adults are reviewed, and systematic and phylogenetic implications are derived from the patterns of variation.
A new genus and species of Hemiptera: Heteroptera: Enicocephalomorpha: Aenictopecheidae: Aenictopecheinae, Ulugurocoris grebennikovi gen. et sp. n., based on micropterous females from Tanzania, Uluguru Mts, Budunki, is described and differentiated. The males are probably macropterous. Some general aspects of morphology of U. grebennikovi are discussed in a broader context, such as presence of cephalic trichobothria (suggested to be a groundplan character of Heteroptera), presence of “gular sulci” (suggested to have an ecdysial function), lack of cephalic neck (symplesiomorphy with other Hemiptera), presence of posterior lobe of pronotum associated with the epimeroid (a new term for so called “proepimeral lobe”), and presence of notopleural sulcus on the propleuron. Diagnostic characters of the Aenictopecheinae are summarized and distribution of their seven genera is reviewed. Ulugurocoris grebennikovi is the first representative of the basal family Aenictopecheidae in the Afrotropical Region. The type locality is situated in the Eastern Arc Mountains (Tanzania), a recently identified hotspot of Afrotropical diversity characterized by a high degree of endemism caused by high rates of speciation combined with low rates of extinction. A brief characterization of the area is provided., Pavel Štys, Petr Baňař., and Obsahuje seznam literatury
Frenae are forewing-holding ridges situated in the Heteroptera parallel to the lateral sides of mesoscutellum, and covered by a squamiform, overlapping, glabrous microsculpture. The situation found in Rectilamina sp. (Dipsocoromorpha: Schizopteridae: Hypselosomatinae) suggests that each single squamiform element is homologous to a strongly modified microtrichium, and that, at least in this case, there is no basic difference between microtrichium and acanthus.
Structures that assist in spreading secretions produced by the metathoracic glands were examined in Reduviidae and Pachynomidae (Heteroptera). The systematic distribution of a row of long and stout setae on the metacoxa, the metacoxal comb, was reinvestigated in a representative sample in both taxa. Observations on living Dipetalogaster maximus (Reduviidae: Triatominae) corroborated the interpretation of this metacoxal comb as an evaporatory device, which assists in atomizing the gland secretions. In addition to the metacoxal comb, a row of stout setae on the metacetabulum - a metacetabular comb - was found in several Reduviidae, which interacts with the metacoxal comb during rotation of the metacoxa. In addition to those atomizing devices, cuticular modifications surrounding the opening of the metathoracic gland, which presumably form evaporatoria, were discovered in Ectrichodiinae. The meshwork-like structure of this cuticle resembles the cuticular modifications found associated with the opening of the Brindley's gland in Reduviidae, but differs from the mushroom-like evaporatoria around the metathoracic glands in most Cimicomorpha and Pentatomomorpha. Thus, two fundamentally different mechanisms to spread secretions of the metathoracic gland - atomization and evaporation - are present in Reduviidae.
Cuticular parts of the spermatheca and associated vaginal structures (chiefly the ring sclerites of the parietovaginal glands) have been examined and compared in 190 cydnid species representing 65 genera and all five subfamilies currently recognized in the family (Amnestinae, Cephalocteinae, Cydninae, Garsauriinae, Sehirinae). Four species belonging to genera formerly included within the Cydnidae (Dismegistus, Parastrachia, Thaumastella, Thyreocoris) were also examined. Morphology of the three main parts of the spermatheca [seminal receptacle (distal bulb), intermediate part (pump apparatus), spermathecal duct] is described. Four main types of spermathecae can be recognized from the distal receptacle and the intermediate part: the amaurocorine type (in Sehirinae: Amaurocorini), amnestine type (in Amnestinae), garsauriine type (in Garsauriinae), and "cydnoid" type (in Cephalocteinae + Cydninae: Cydnini, Geotomini + Sehirinae: Sehirini). No synapomorphy of these types was found which suggests that the currently conceived Cydnidae are not monophyletic. Moreover, out of these four types only the "cydnoid" is typically pentatomoidean due to the presence of an intermediate part usually well delimited by two flanges and having always an unsclerotized flexible zone as well as two internal cuticular structures (septum and fretum) partly obstructing the lumen. The simple tubular amaurocorine type is unusual and aberrant within all Pentatomoidea. The amnestine and garsauriine types display some similarities with taxa outside the Pentatomoidea, especially with some lygaeoid or coreoid spermathecae, mainly in the structure of the intermediate part not delimited proximally (absence of flanges) and devoid of the flexible zone. Within the "cydnoid" type, six spermathecal facies can be characterized principally according to the shape of both the apical reservoir along with the intermediate part, and the differentiations of the spermathecal duct. It has been impossible to find any synapomorphy for all species and for the six facies belonging to the "cydnoid" type of spermatheca. We suggest that the Cydnidae as defined presently are probably a polyphyletic group; moreover its main "cydnoid" branch, called by us Cydnidae sensu stricto (Cephalocteinae + Cydninae + Sehirinae: Sehirini) seems to be relatively recent among the Pentatomoidea. Nishadana and Nishocoris are transferred from Garsauriinae back to Cydninae: Cydnini and the tribe Amaurocorini (Sehirinae) is upgraded to a separate subfamily Amaurocorinae stat. nov. Moreover, we regard the Geotomini and the Sehirini both as non-monophyletic and we indicate that by appending them sensu lato (Geotomini "s. l.", Sehirini "s. l.")
Cephalic chaetotaxy of nymphal and adult stages of species from all the subfamilies of Cydnidae s. str. (sensu Froeschner, 1960 and Lis, 1994), namely Garsauriinae, Cephalocteinae, Cydninae, Sehirinae, and Amnestinae, was studied. Two types of setae, primary and secondary, are described, and changes they undergo during ontogeny reviewed. The adaptive, taxonomic and phylogenetic significance of the cephalic setae in the Cydnidae s. str. is discussed. A ground-plan of the original cephalic chaetotaxy of the family, and its evolution within the family Cydnidae s. str. are proposed.
Sensillar structures of the antennal pedicel are investigated in Reduviidae and Pachynomidae. The cave organ, a presumably chemoreceptive structure, previously reported only for haematophagous Triatominae, is described here also for representatives of Peiratinae, Reduviinae and Stenopodainae. The systematic implication of the occurrence of this sensillar structure is discussed. Further, four sclerites located in the membrane between pedicel and preflagelloid are described and used as landmarks for the recognition of individual trichobothria in Reduviidae and Pachynomidae. Characters of the trichobothrial socket are studied and discussed systematically. Homology of the distalmost trichobothrium of Reduviidae with the single trichobothrium in Pachynomidae is proposed. This hypothesis is based on the structure of the cuticle surrounding the trichobothria and on the trichobothrial position relative to the four sclerites of the pedicello-flagellar articulation. The single trichobothrium present in most nymphs corresponds to the distalmost trichobothrium in adult Reduviidae in position and structural detail. A reasonable hypotheses on the homology of individual trichobothria of the proximal row or field seen in most Reduviidae can so far only be formulated for Peiratinae.