The present paper describes the sensory structures on the apical segment of the labium in fifteen fulgoromorphan families (Hemiptera: Fulgoromorpha), using the scanning electron microscope. Thirteen morphologically distinct types of sensilla are identified: five types of multiporous sensilla, four types of uniporous sensilla and four types of nonporous sensilla. Three subapical sensory organ types are also recognized, formed from one to several sensilla, each characteristic of a family group. Sensilla chaetica (mechanoreceptive sensilla) fall into three categories dependent on length and are numerous and evenly distributed on the surface of the labium except where they occur on specialized sensory fields. The planthopper morphological ground plan is represented by two apical pair of sensory fields (dorsal and ventral) on which 11 dorsal pairs of sensilla (10 peg-like pairs + 1 specialized pair dome or cupola-like) and 2 ventral pairs of sensilla basiconica occur. Two main patterns (cixiid and issid) together with more specialized ones (derbid, lophopid, flatid and fulgorid) are reported. Disparity and diversity of the sensory structures are analyzed from a taxonomic and functional perspective. A gustatory function is provided for several chemoreceptive labial sensilla, as in the antennal flagellum sensilla in some other Hemiptera. This represents a more recently evolved function for the planthopper labium. Finally, further lines of study are suggested for future work on the phylogeny of the group based on the studied characters.

The external morphology and distribution of the antennal sensilla of 21 species from five families of semiaquatic bugs (Gerromorpha) were examined using scanning electron microscopy. Nine main types were distinguished based on their morphological structure: sensilla trichoidea, sensilla chaetica, sensilla leaflike, sensilla campaniformia, sensilla coeloconica, sensilla ampullacea, sensilla basiconica, sensilla placoidea and sensilla bell-mouthed. The specific morphological structure of one type of sensilla (bell-mouthed sensilla) was observed only in Aquarius paludum. Several subtypes of sensilla are described, differentiated by number, location and type of sensillum characteristic for each examined taxon. The present study provides new data about the morphology and distribution of the antennal sensilla in Gerromorpha.

The present paper describes sensory structures on the apical segment of the labium in representatives of the subfamily Peiratinae (Heteroptera: Reduviidae), using the scanning electron microscope. The study is based on dry material representing 19 species and 16 genera. Within Peiratinae thirteen morphologically distinct types of sensilla were identified. Among them were four new types of sensilla (porous placodea sensillum [PPLS], multilobate sensillum [MS], domeelongated sensillum [UDES], and pit peg sensillum type 2 [NPPS2]) were found. Mechanosensilla are evenly distributed on the surface of the labium and form a characteristic pattern in various species. The main characters of the third visible (apical) segment of the labium are: presence of different sized sensilla of the chaetica type 1, 2, and 3; trichodea sensilla (TS); campaniform sensilla (CS); and various types of nonporous pit peg sensilla (NPPS1, NPPS2, and NPPS3). Distally on the apical segment of the labium dome-elongated sensilla (UDES) there are a characteristic arrangements, described as (3+3) and (1+2). Chemical sensilla are grouped on the tip of the labium. The position, number, and types of chemical sensilla on this area are very similar in all studied species.

Scanning electron microscopy and light microscopy were used to elucidate the morphology of labium and mandibular and maxillary stylets of the aphids Stomaphis quercus (L.) and S. graffii Cholodkovsky. The mechanism of labium shortening associated with feeding process was described as well. Stomaphis quercus and S. graffii have cone-shaped labium of 13 and 10 mm in length, respectively, that strongly extend behind the abdomen. The stylets bundle comprises a pair of mandibular and maxillary stylets which are on average as long as labium. Serial cross sections of labium revealed that the first segment is inverted inside and the second is pulled into it; both segments are shifted into abdomen. This study provides new information on S. quercus and S. graffii mouthparts that may help to understand their feeding behavior.

The present study provides new data on the morphology and distribution of the labial tip sensilla of 41 species of 20 gerromorphan (sub)families (Heteroptera: Gerromorpha) obtained using a scanning electron microscope. There are eleven morphologically distinct types of sensilla on the tip of the labium: four types of basiconic uniporous sensilla, two types of plate sensilla, one type of peg uniporous sensilla, peg-in-pit sensilla, dome-shaped sensilla, placoid multiporous sensilla and elongated placoid multiporous sub-apical sensilla. Based on their external structure, it is likely that these sensilla are thermo-hygrosensitive, chemosensitive and mechano-chemosensitive. There are three different designs of sensilla in the Gerromorpha: the basic design occurs in Mesoveliidae and Hebridae; the intermediate one is typical of Hydrometridae and Hermatobatidae, and the most specialized design in Macroveliidae, Veliidae and Gerridae. No new synapomorphies for Gerromorpha were identified in terms of the labial tip sensilla, multi-peg structures and shape of the labial tip, but eleven new diagnostic characters are recorded for clades currently recognized in this infraorder. One synapomorphy is recorded for Hydrometridae + Hermatobatidae + Macroveliidae + Veliidae + Gerridae; five for Macroveliidae + Veliidae + Gerridae; one for Veliidae + Gerridae; and one for Gerridae alone. Within Gerridae, one possible autapomorphy is recorded for Trepobatinae, and two possible autapomorphies for Rhagadotarsinae. We also record a possible autapomorphy for Cylindrostethinae, which indicates that this taxon is monophyletic, as is indicated by other morphological characters. Finally, we record one putative diagnostic character for Macroveliidae + Veliidae, two families that are otherwise not considered sister groups. This new set of characters based on features of the mouthparts of gerromorphan bugs might provide new insights into the cladogenesis of the infraorder.