Comparative Analysis and Systematic Mapping of the Labial Sensilla in the Nepomorpha (Heteroptera: Insecta)

The present study provides new data concerning the morphology and distribution of the labial sensilla of 55 species of 12 nepomorphan families (Heteroptera: Nepomorpha) using the scanning electron microscope. On the labial tip, three morphologically distinct types of chemosensilla have been identified: two types of papillae sensilla and one type of peg-in-pit sensilla. Twenty-one morphologically distinct types of the mechanosensilla as well as two types of the trichoid sensilla (contact-chemoreceptive sensillum) have been identified on all labial segments in representatives of subfamilies. In Nepomorpha, morphological ground plan of the labial sensory structures is represented by an apical sensory field with 10–13 pairs of papillae sensilla and the peg-in-pit ones placed more laterally; numerous trichoid sensilla are placed on the IV segment; the chaetica sensilla are present and placed in groups or rows distributed along the labium near the labial groove on the dorsal side, and also several chaetica sensilla are unevenly scattered on the surface of that segment; the cupola and peg sensilla are numerous and evenly scattered on the fourth labial segment; the prioprerecptive sensilla, one pair is positioned on the dorsal side and on the fourth segment of the labium. The new apomorphical characters have been established for the labial sensilla in the Nepomorpha.


Introduction
The mouthparts of the hemipteran insects are organs connected with feeding, comprising the unpaired labrum in the front, a median hypopharynx behind the mouth, a pair of mandibles and maxillae laterally, and usually a segmented labium [1,2]. The sensory system, which mediates feeding, is used for external detection of the surface of plants or animals and host acceptance by antennal or labial sensilla (gustative and contact-chemoreceptive ones). All hemipterans have a large number of various antennal sensilla, and they are probably used to detect olfactory cues during long-distance orientation to the host plants. In the case of the labium of the hemipteran insects, the apical segment with the apical sensilla plays a role in recognizing the outer surface of the plant or animal food source, while the inner sensory organ (e.g., precibarial sensilla) comes directly into contact with the food as it is ingested [3][4][5]. These sensilla belong to the group of chemosensilla (gustative sensilla); they have a single relatively large pore at the tip (i.e., uniporous sensilla) and are sunken in inflexible sockets, distinguishing them from olfactory sensilla that have many small pores; they are called multiporous sensilla and are also sunken in inflexible sockets [6,7]. Contact chemoreceptives have various forms, which are described as the trichoids, bristles, pegs, basiconica, spots, pits, and domes. All of these have a pore on the exterior and are innervated by neurons with features characteristic of chemo-and mechanoreceptors; their base can be distinctly sunken in flexible sockets [4,6,8]. Moreover, the surfaces of all labial segments are usually equipped with various sensory structures by which different signals from the environment are detected. The most common among those is the tactile structures which greatly vary in form, including the hair-shaped bristles, chaetica, trichodea, trichobothria, pegs, dome-like, and campaniform sensilla and representing a large group of mechanosensilla. These sensilla are without pores and are attached to the labium in a socket by an articulation membrane [4,6,8].
In most of the Nepomorpha, the labium consists of four segments more or less extended and is directly exposed to 2 The Scientific World Journal water [1,2,9]. Solely in the Corixoidea, the labium is more or less triangular, much shorter and dorsally bears a deep stylet groove flanked by a series of sclerotized transverse bands [10][11][12]. These transverse bars are separated from each other by slightly sclerotized membranes in which the sense organs are located [10,13,14]. In particular, in the heteropterans the tips of the labium (two lateral lobes) have gustative sensilla, frequently the contact chemoreceptive sensilla, and rarely also the olfactive, hygro-, and thermoreceptive sensilla as well as the tactile sensilla [1,15,16]. Several types of these sensilla on the labial tip have been described in many species of the Pentatomomorpha [17][18][19][20][21][22][23], the Nepomorpha [1,24] and the Gerromorpha [Brożek and Zettel, in prep]. A full documentation of different cuticular hairy structures of the mechanosensilla and chemosensilla on all segments of the labium in several species of the Triatominae (Cimicomorpha: Reduviidae) has been presented by Catalá [25] and on distal segment of the labium in the Peiratinae (Cimicomorpha: Reduviidae) by Brożek and Chłond [15]. A comprehensive study of the Triatominae and the Peiratinae species has shown that the types of the labial mechanosensilla and their numbers are similar in individual species. Such information can be used to compare their labial sensilla with those found in other groups of the Heteroptera. Documentation of the presence of different types of labial sensilla in a large set of taxa will result in a concise picture of the systematic distribution of this structure across the Nepomorpha, which may prove useful for future systematic analysis. The scanning electron microscopy will refine the picture of fine structural details of the labial sensilla in the studied nepomorphan groups.
The study aims to provide an insight into the sensilla on the labium in representatives of the Nepomorpha and attempts to clarify if the discovered types of the sensilla and their distribution have a phylogenetic value for the water bugs.

Taxon Samples.
This study of labial sensilla was based on dry material consisting of adult specimens from the collections of the Natural History Museum in Vienna, Zoological Museum of the State Moscow University, and the Paleontological Institute of the Russian Academy of Sciences in Moscow. The basal part of the head with a part of the rostrum or the whole specimens was glued onto a scanning electron microscope stub. The labial sensilla used for SEM photographs were not coated; the photographs were taken with a Hitachi scanning electron microscope, with the samples placed in the low pressure chamber.
Classification and order of families and subfamilies listed below are the same as that established byŠtys and Jansson [26], except for the Micronectidae and the Diaprepocoridae which have been elevated to the rank of family [27].
In the part of discussion, the ground plan of the morphological labial sensilla structures and the preliminary estimation of the characters of the labial sensilla in respect to phylogenetic value are compared with the basal model within the group (i.e., the basal taxa of the Nepidae and Belostomatidae) to the more diverse forms of these structures in more evolutionarily advanced groups (i.e., Corixidae, Ochteridae, Gelastocoridae, Aphelocheiridae, Naucoridae, Pleidae, Helotrephidae, and Notonectidae, resp.). Specimens of the Potamocoridae were not available for the purpose of the present study.

Terminology Used for Descriptions of the Apical Sensilla.
With respect to the external morphology of the sensilla, in this study they are classified according to the morphological criteria established by Altner and Prillinger [6], McIver [8], and Zacharuk [7]. The receptor functions of the sensilla of the insects have been distinguished based on the morphological and ultrastructural features described by a number of authors [4, 6-8, 28, 29]. Such information is also used for the interpretation of newly described labial sensilla such as clubbed-like sensillum (CBS), paddle-like sensillum (PDS), cupola-like sensillum (CUS), finger-like sensillum (FRS), freniale-like sensillum (HLS), chaetic sensillum with a divided tip (CHD), star-like sensillum (STS), and multilobed sensillum (MPS). The remaining types of sensilla mentioned in the present paper (Table 1)   previous descriptions of other authors [4, 6-8, 15, 24]. Table 1 includes information about functional and morphological classifications and provides definitions of the sensilla of insects used for current descriptions of the twenty-four types of labial sensilla in the Nepomorpha. Abbreviations of sensilla used throughout the paper are explained in the last column.

Morphology and Categories of the Labial Sensilla.
Functionally, the labial sensilla are classified into two categories: mechanoreceptive and chemoreceptive sensilla, within which there can be determined twenty-four types ( of their external appearance and location. The main external morphological characters indicating the types of sensilla are pores system (visible or not), the manner in which the sensilla are sunken with respect to the surface of the labium (flexible or inflexible sockets), and the shape of the sensilla.
In addition, structures similar to sensilla have been reported as unidentified type (PLE). (Tactile Sensillum). Chaetic sensilla (CH) (Figures 1(a), 1(b), and 1(c)) occur in different lengths and are sunken in a circular socket on the labial surface. Their external surface is usually grooved without pores. Based on the aforementioned character of morphology the three subtypes are differentiated as follows.

Mechanoreceptive Sensillum Sunken in Flexible Socket
Large (100 m and above) chaetic sensilla (CH1). The sensilla are long, relatively straight, gradually tapering and slightly curved at the tip (Figure 1(a)).
The chaetic sensilla are present in all examined species in various parts of the labium.
Conical Sensillum (COS): a Prioprereceptor (Figure 1(d)). This sensillum is a short or long cone with a smooth surface. It is sunken in a dome-shaped socket (ds).

Characteristic Forms of the Mechanosensilla
Squamiform sensillum (SQS) (Figure 1(e)). This sensillum is slightly rhombic-shaped and has been found in the Nepinae (Laccotrephes japonensis, Figures 9(d) and 9(f)) as well as in Curicta granulosa, Borborophyes mayri, and Nepa cinerea ( Table 2). Trichobothrium sensillum (TBS) (Figure 1(e)). A hair ("trich" = hair) is long and tapering at the end. Its basal part is sunken in a socket. The flexible socket (Soc) is rounded and is placed on a dome-like cuticular elevation (= bothrium (bt)). The hair is oriented at a more or less right angle to the cuticle. The cuticular surface surrounding the trichobothrium is usually devoid of other sensilla. Several trichobothria have been observed only in the Nepinae (Laccotrephes japonensis, Figures 9(d) and 9(f)), as well as in Curicta granulosa, Borborophyes mayri and Nepa cinerea.
Basiconic sensillum (BAS) (Figure 1(e)). The sensillum is tapered gradually from a wide base to the tip and is relatively stiff. This sensillum has been found in the Nepinae (Laccotrephes japonensis (Figure 9(d)) as well as in Curicta granulosa, Borborophyes mayri, and Nepa cinerea.
Clubbed-like sensillum (CBS) (Figure 1(f)). In this sensillum the base and shaft have the same width and the tip is slightly rounded. This type of sensillum has been noticed in the Nepinae (Laccotrephes japonensis (Figures 9(a), 9(b), and 9(c)) as well as in Curicta granulosa, Borborophyes mayri, and Nepa cinerea.
Paddle-like sensillum (PDS) (Figure 1(g)). This sensillum is narrow in its lower part, then gradually expands up to a wide, flattened tip. Two sizes of this sensillum are Cupola-shaped sensillum (CUS) (Figure 2(a)). This sensillum is short and protrudes slightly above the surface of the labium. This type has been identified in the Belostomatidae Peg sensillum (PES) (Figure 2(a)). It is a short cone sunken in a shallow cavity of cuticle and equipped with a flexible socket (SOC). This type of sensillum has been found in the Belostomatidae (Belostoma flumineum Figure 11 Finger-like sensillum (FRS) (Figure 2(b)). The base and tip of this type of sensillum are of the same width, but the shaft is slightly wider in the middle. This type of sensilla has been observed only in the Gelastocorinae (Gelastocoris oculatus Figure 16(f)).
Chaetic sensillum with a bisected tip (CHB) (Figure 2(d)). The tip of the seta is divided into two short branches. This type of sensillum has been found only in the Nerthra nepaeformis ( Figure 17(e)) (Gelastocoridae: Nerthrinae).
Star-like sensillum (STS) (Figure 2(e)). It is a short cone divided into four or five narrow lobes. The base of the sensillum is sunken in a socket, and it is situated shallowly in a cavity. The lobes are prominent above the cuticular surface. This type of sensillum has been specific to the Aphelocheiridae (Aphelocheirus aestivalis, Figures 18(c), 18(d), and 18(e) and A. variegatus).
Multilobed sensillum (MPS) (Figure 2(f)). This type of sensillum consists of a few narrow lobes, arising from a common stem. The base of the sensillum is sunken in a socket and the lobes evidently protrude above the cuticular surface.     Figure 24(g)) as well as in Ilyocoris cimicoides and Pelocoris femoratus, ( Table 2).
Ribbon-like sensillum (RBS) (Figures 3(a), 3(b), and 3(c)). The shaft of this sensillum is a long, wide, and flexible lobe with a blunt ending. The base is slightly narrower than the shaft and is sunken in the socket. These sensilla have different lengths. A long sensillum of this type is 7.5 m (RBS1) whereas its short counterpart (RBS2) is 4.0 m. Both types of sensilla are numerous and have been found in the Corixidae, (Corixa dentipes, Figure 29 The unidentified type (PLE) has been found only in Limnocoris lutzi (Figure 21, Limnocorinae) and Cryphocricos hungerfordi (Figure 22, Cryphocricinae). These structures are small plates with several peg-like endings. They are distributed on the surfaces of the first, second, and third segment, but not on the fourth segment of the labium.

Contact-Chemoreceptive Sensillum Sunken in a Flexible
Socket. Trichoid sensillum is a contact chemoreceptive sensillum (TRS) (Figures 4(a)-4(d)). Trichoid sensilla are usually strong setae placed in shallow depressions in flexible sockets. They are often slightly curved just above their bases and protrude at low angles (about 20 ∘ in the case of a dorsal and 50 ∘ in the case of a ventral trichoid sensillum) from the base towards labial tip (Figures 4(a), 4(b), and 4(c)). They have a smooth surface and are tapered distally. The terminal pore is visible and therefore these sensilla should be considered as contact-chemoreceptive sensilla; this is also suggested by their location. Trichoid sensilla (TRS) are, respectively, subdivided into two groups according to their size (length; large TRS1, short TRS2) and into three groups according to their location. Large

Peg-in-pit sensillum (PIP) is a thermohygroreceptive sensillum (Figures 5(c) and 5(d)
). This type of sensillum has a small peg inserted in a round deep depression. The walls of the sensillum are smooth without pores. One such sensillum is present on the lobes (sensory fields) ( Figure 5(g)) and usually is situated either centrally or more laterally; however, it is not always visible in some studied species. Generally, this type of sensillum is observed frequently in the species of the Nepidae (Figure 9  tip is divided into a few furrows, which probably in most species is hiding this type of sensillum, which is, however, visible in the Pleidae (Paraplea frontalis, Figure 25(f)), Helotrephidae (Hydrotrephes visayasinensis, Figure 26(f)), and Notonectinae (Notonecta glauca, Figure 28(f) sensillum no 6). Sensilla of this type are distributed only over the labial tip.
3.6. Organization of the Labium. In most of the aquatic bugs, the elongated labium is divided into four segments (I, II, III, and IV) except for in the Corixidae, Diaprepocoridae, and the Micronectidae. In the latter families the labium is short and wide, and the segmentation of the labium is not visible. The tip of the labium (one half) is slightly triangular with a clearly wrinkled (folded) surface. In the remaining (c) The papillae sensilla (PAS2) are present in the number of 8-14 pairs. They are sunken in the cuticle, and folds are formed around them. The PIP sensilla are not evident; however, in some species they are visible ( Figure 24(e)). This type of distribution has been observed in the Gelastocoridae (except the Nerthrinae where the tip is smooth; (Figure 6(h))), Naucoridae, and Notonectidae (Figures 6(g), 6(j), 6(k), and 6(n)).
(d) One pair of pit sensilla is placed centrally together with two PAS2 on the round convex surface, while the remaining papillae sensilla (PAS2) in the number ranging from 8 to 11 pairs are distributed around them. This pattern has been found in the Pleidae and Helotrephidae (Figures 6(l) and 6(m)).
(e) The papillae sensilla PAS2 are more numerous and visible on the triangular labial tip. They are spread unevenly in cuticular folds. This type of distribution of the sensilla is specific to the Corixidae and Micronectidae. Only in the Diaprepocoridae the sensilla (PAS2 and PES) are sunken deep in the smooth surface of the tip (Figures 6(o), 6(p), and 6(q)). The peg sensilla (PES) and ribbon-like sensilla (RBS2), however, are present at the labial tip; these are mechanosensilla.

Distribution Types of the Mechnosensilla and Contact-Chemoreceptive Sensilla on the Labial Segments in the Systematic Groups.
The presence or absence of different types of mechanosensilla on the labium in the 55 species is presented in Table 2. A distinction of general types of distributions of the mechanosensilla in taxonomic groups is as follows.
3.8.1. Sensilla Numerous, Grouped, and Unevenly Arranged on the Labium (Figure 7(a)) The Belostomatidae. On the labial segments (I, II, and III) the sensilla chaetica (CH1, CH2, and CH3) are numerous and placed in groups or rows distributed along the labium near the labial groove on the dorsal side; apart from that several chaetica, sensilla are unevenly scattered on the surface of those segments ( Figure 11(e)). On the IV segment the sensilla (CUS and PES) are numerous and unevenly scattered. Similar distribution can be found on the ventral side with less numerous sensilla. More differences in distribution of the sensilla can be observed in Limnogeton fieberi ( Figure 13). The II and III segment on the dorsal and ventral sides are densely covered by short sensilla CH3; however, on the dorsal side near the labial groove sensilla CH1 and CH2 are also numerous. These sensilla (CH1, CH2 and CH3) are placed dorsally and form a dense layer. Trichoid sensilla (two dorsal pairs and three ventral pairs) are similarly placed in both subfamilies (Belostomatinae and Lethocerinae), subapically on the IV segment but in various numbers and size (Table 2).

Sensilla Densely and Evenly Arranged on Labium (Figures 7(b), 7(c), and 7(d))
The Nepinae. On the labial segments (II, III: I-the first is invisible) the sensilla (SQS) are numerous and totally cover the surface of the segments to form a main layer with several of the BAS, TBS, and CH1 sensilla. On the IV segment the sensilla (CBS) are less numerous and are evenly scattered.  (Figure 26(a)).

Sensilla Are Very Numerous and Arranged in Transverse Bands or Scattered Unevenly on the Labial Surface (Figures 8(a), 8(b), and 8(c))
The Corixidae (except for the Cymatiinae), Micronectidae, and Diaprepocoridae. The sensilla (RBS1, RBS2) are distributed in several transverse bands (BD) on the triangular-shaped labium. In the Corixidae there are six transverse bands, in the Micronectidae there are four bands, while in the Diaprepocoridae there are two and a half bands. One band consists of two rows (r1, r2) of the semicircular grooves (GS) with one row of pore (p) (r3) and two rows (r4 and r5) of ribbon-like (RBS2, RBS1) sensilla. Peculiar characters have been observed in the Cymatiinae, where the sensilla are scattered over the smooth surface of the labium (RBS1, RBS2, and PES). Chaetica sensilla (CH1, CH2, and CH3) are distributed on the lateral and ventral sides. The trichoid sensilla (PES) have not been observed.

Plan Distribution of the Prioprereceptive Sensilla (COS).
The one pair of prioprereceptive sensilla (COS) is restricted to the dorsal side of the second and fourth segments of the labium in most nepomorphan species, except for the Corixoidea (these sensilla have not been found). In the proximal part of the second and fourth segment there is usually one pair of the prioprerecptive sensilla located dorsally near the rear edge of the segment. However, in the Nerthrinae three pairs are visible on the second segment. In Limnocoris lutzi COS are present in three locations. Two (or four) of the COSp are on the external distal edge of the II segment, and one is placed internally closer to the labial groove ( Figure 21(f)). Two COS-d sensilla are situated in the middle of the II segment on the proximal edge. The prioprereceptive sensilla on the ventral side of the labium between I and II segment are visible in the Helotrephidae.

Discussion
The present study carriers out a comparative analysis of the labial sensilla in water bugs, the Nepomorpha. The labium is equipped with a set of sensilla, including a large group of different types of the mechanosensilla and a smaller group of the chemosensilla.

The Sets and Distribution
Types of the Labial Sensilla in the Nepomorpha. The total number of chemosensilla at the tip of the labium and the plan of their distribution allows the recognition of five main groups in the Nepomorpha and supplies evidence for the relationships between these groups. The first group consists of belostomatids, nepids, and the Nerthra. However, the Nerthra systematically belongs to the Gelstocoridae and it is rather unexpected that it shows similarity of the labial tip sensilla to those found in belostomatids and nepids. The second group includes the ochterids and aphelocheirids. The third group includes the representatives of gelastocorids, naucorids, and notonectids whereas in the fourth group there are pleids and helotrephids. The fifth group is totally different from the above-mentioned types. In the Corixoidea, the triangular labial tip has several PAS2 and PES sensilla, unevenly spread. In this hierarchy of the discussed taxa there can be seen general conformation of families or groups of families to the pattern of close relationships, which have been indicated in previous studies conducted by other researchers [30][31][32].
The trichoid sensilla are usually present in most taxa but in different numbers (Table 2). They are located on the dorsal and ventral surfaces on the fourth segment of the labium (near the apex) in the families of Belostomatidae, Pleidae, Helotrephidae, and Notonectidae. In addition, in the Nepidae trichoid sensilla are present also on the lateral sides near the apex. In three other families, namely, the Ochteridae, Gelastocoridae, and Aphelocheiridae these sensilla are observed only on the ventral side of the fourth segment. Furthermore, other differences are visible also in the Naucoridae, where the trichoid sensilla are situated on the third segment of the labium in the dorsal position, but ventrally they are situated on the fourth segment. In the Corixoidea the trichoid sensilla have not been recognized. Probably they are not visible being hidden in the dense layer of the chaetica sensilla.
The most conspicuous and common in the water bugs (Belostomatidae, Nepidae, Naucoridae, Pleidae, Helotrephidae, and Notonectidae) are chaetica sensilla covering the first, second, and third labial segment. In four cases chaetica sensilla are also present on the fourth segment of the labium for example, in the Nepidae, Pleidae, Helotrephidae, and Notonectidae. Moreover, the chaetica sensilla are restricted only to the first and second labial segments in the Ochteridae and Aphelocheiridae. Generally, the chaetica sensilla (CH1, CH2, and CH3) are distinctly differentiated on the dorsal and ventral surfaces of the labium and placed in small tufts in narrow rows and frequently are scattered unevenly on both surfaces. The major difference between the chaetica sensilla in the Belostomatidae and the chaetica sensilla in the remaining families is that in the case of chaetica sensilla in all examined species of the Belostomatidae there are distinct areas where they are present (the sensilla are grouped on the dorsal side of the I and II segment or arranged along the groove of the labium on the III segment) and these sensilla are numerous in contrast to those scattered all over the surface of the labial segments in some remaining taxa, except for the Pleidae, Helotrephidae, and Notonectidae. In the above-mentioned taxa the system of distribution of the sensilla is similar to the Belostomatidae, but the sensilla are less numerous. The evidently different pattern of distribution of the chaetica sensilla (densely spread over the lateral side of the labium and around the membranous labial tip) can be seen in the Corixoidea. However, several shapes of mechanosensilla different from the chaetica sensilla have been noted in representatives of different subfamilies (Table 2). Among nepomorphan taxa in the Nepidae the squamiform sensilla and paddle-like are typical only in the Limnocorinae, Cryphocricinae, and Naucorinae, whereas ribbon-like senilla (RBS1, RBS2) have been documented only in the corixoids. The term "ribbonlike sensilla" in this paper has been adopted from that used by Brożek [24]. Earlier works [10,13,14] used the term "peg sensilla" for the sensilla placed in transverse bands in the corixids, however, the latest observations of the shapes of these sensilla have lead to a conclusion that their shapes distinctly deviate from the shape of a peg. The prioprereceptive sensilla (COS) are visible in most nepomorphan species except for the Corixoidea. Their position on the dorsal side of the fourth segment of the labium is generally stable in most representatives of the Nepomorpha. In the proximal part of the third segment there is usually one pair of the prioprerective sensilla, located dorsally near the rear edge of the segment. However, only in the Nerthrinae

The Ground Plan of Nepomorphan Labial Sensilla. The
Belostomatidae and Nepidae have been coded as taxa possessing basal characters in the ground plan of the morphological approach used by Rieger [33], Popov [2], and Mahner [32] as well as the approach developed by Hebsgaard et al. [30] combining morphological and genetic data. Thus, some of the characters in these taxa may theoretically represent a plesiomorphic condition.
In the absence of data on the labial sensilla from the outgroup (the Enicocephalomorpha have been proposed as a basal outgroup byŠtys [34,35], Schuh and Slater [9], after Wheeler et al. [36] and in this study the nepomorphan ground plan of the labial sensilla is modeled on the sensory equipments of the Belostomatidae and Nepidae represented by the following six sensilla structures: (1) apical sensory field with 10-13 pairs of papilla-like sensilla (PSA1); The Scientific World Journal (2) apical sensory field with the peg-in-pit (PIP) sensilla placed rather laterally on the sensory field; (3) numerous trichoid sensilla placed on the IV segment on the dorsal, lateral and ventral sides; (4) chaetica sensilla (CH1, CH2, and CH3) present and placed in groups or rows distributed along the labium near the labial groove on the dorsal side and also several chaetica sensilla unevenly scattered on the surface of that segment;  In all analyzed species (fifty five), it has been discovered that the labial tip sensilla are very similar and a common pattern can be established for species which belong to the same family or group of families that are closely related. Consequently, for nepomorphan taxa the five patterns of the distribution of the labial tip sensilla can be presented (above). In comparison with the other heteropteran infraorders it has been observed that the morphology and distribution of the labial tip sensilla in the Nepomorpha are distinctly varied with respect to what has been reported in the Gerromorpha (Brożek and Zettel, in prep), Pentatomomorpha [19,21], and Cimicomorpha: Reduviidae [15,25]. In terms of diversity and abundance of the sensory system on the labial tip, the Nepomorpha come second to the Gerromorpha. In gerromorphan bugs a richer and more diverse sensory equipment (several morphological types of sensilla) has been detected [Brożek and Zettel, in prep]. An undifferentiated sensory system occurs in the Pentatomomorpha (e.g., Dysdercus fulvoniger and D. koenigii, D. fasciatus, D. intermedius, Lygus lineolaris, and Neomegalotomus parvus), where the labium tip usually represents one morphological type of basiconic sensilla functioning as the contact-chemoreceptive sensilla (several pairs), basiconic gustative sensilla (several pairs), and basiconic olfactive sensilla (one or two pairs) [17,19,21,22,37]. In some of the Reduviidae one type of peg and peg-inpit sensilla have been noticed [15,25,38]. Furthermore, two types of mechanosensilla (small hairs and long bristles) have been identified on the tip of the labium by Bernard [39]. The chaetica sensilla on labial segments in the Nepomorpha (i.e., Belostomatidae, Corixidae, some of Naucoridae, Pleidae, Helotrephidae, and Notonectidae) closely resemble these in the Reduviidae (Peiratinae and Triatominae) [15,25] as well as in other hemipteran groups, for example, the Fulgoromorpha and Cicadomorpha [40][41][42]. Other nepomorphan taxa (Nepidae, Gelastocoridae, Aphelocheiridae, and some of the Naucoridae) have modified base and apical "hairs", which represent various forms of mechanosensilla. Examples for various types of hairs are found in many insects [8], where the tip of the hairs is enlarged, disk-shaped, or divided. Probably the large variety of labial types of mechanosensilla of the Nepomorpha can indicate that the sensilla evolved several times within that group and they can be interesting as a phylogenetic signal. The inspection of chaetica sensilla in the nepomorphans suggests that the number and type of their distribution are quite diverse among species. Similar data have been obtained during the observation of chaetica sensilla in several species of the Triatominae [1,25,38,43]. The more established pattern of the distribution of chaetica sensilla on the apical segment of the labium has been documented in the Peiratinae: 19 species were revealed to represent three patterns of distribution [15]. According to the present study, the type of the arrangement of chaetica sensilla with the other type of mechanosensilla recognized on the subfamilies level is stable. Consequently, five possible types for particular taxa have been reported (see above). Previous examination of the species representing the Peiratinae and Triatominae [15,25,38] have shown a lower number of the trichoid sensilla (one or two pairs in all species) on the dorsal and ventral sides than is observed in most nepomorphan taxa. Presently, the study corroborates and broadens the range of distribution of the trichoid sensilla in some nepomorphan species previously described by Brożek [24]. The trichoid sensilla are characteristic with respect to their number and position on the labium in different species in particular families ( Table 2). Judging from the way the trichoid sensilla are oriented and bent in the basal and apical positions, the hairs on the ventral and dorsal side are the first to touch the victim in most nepomorphan species. The trichoid sensilla and long chaetica sensilla (type 1) situated on the labium in the Reduviidae work in a similar way [25]. However, in four nepomorphan taxa (Ochteridae, Gelastocoridae, Aphelocheiridae, and Naucoridae) the identification of victims is performed only by the ventral trichoid sensilla. In this case, it can be explained that different species show different responsiveness to host movements, which might be related to the types and numbers of sensilla present. It is known that there are variations in feeding strategies in hemipteran insects, and these strategies are strongly correlated with taxonomic position and therefore have evolved in distinct patterns [1,25,44]. In connection with this fact it is logical that the sensory systems that mediate feeding have also evolved in patterns. The sensilla used to detect external plants or animals, responsible for the cues to host orientation and host acceptance (antennal and labial sensilla), are highly variable among species of the different taxa [40,41]. Similar conclusions have been reached for other groups of insects [4].

Evaluation of the Significance of the Characters of Labial
Sensilla in the Systematic Groups. The cladistic analysis of morphological and molecular data on the Nepomorpha given by Hebsgaard et al. [30] and the analysis of their mitochondrial genome presented by Hua et al. [31] provide very different relationships proposals of the families.
Providing new characters can significantly influence the future cladistic analysis of the Nepomorpha. A wide variety of labial types of sensilla, especially mechanosensilla, are observed among the Nepomorpha, and their types of distribution can indicate that sensilla have evolved several times within that group and they can bear high phylogenetic signal together with the other characters. However, the current study, limited to the one set of features, is insufficient to 28 The Scientific World Journal form a new phylogenetic hypothesis. The presented data on sensory organs characters do not allow to support or reject the proposals of Hebsgaard et al. [30] and Hua et al. [31] and also of older studies [2,32,33]. Obviously, several significant indications regarding the relationship of certain families of the Nepomorpha can be pointed out based on the current characters (apomorphies).  III   CH2  I  II  III  IV   COS   CH3   CH2   TRS1   CH3   CH2   CH3  CH3   COS   IV   III  II  I   CH3   CH3   CH3   TRS1   COS   3   TRS1   PAS2   7  regarded as ones that have evolved from plesiomorphous peglike sensilla or/and cupola sensilla.
The recognition of four types of sensilla (SQS, TBS, BAS, and CBS) in the Nepinae and the paddle-like sensillum (PDS) in the Ranatrinae has been estimated as autapomorphies of these taxa. The squamiform sensillum (SQS), in the Nepinae, is probably homologous to the paddle-like sensillum in the Ranatrinae. Both types (SQS and PDS) are evidently similar morphologically; they are sunken into the surface and clearly numerous. In addition, they densely cover the whole surface of the labium. The clubbed-like sensillum (CBS) slightly protrudes from the surface and has probably evolved from the peg sensilla of the Belostomatidae. The basiconic and trichobothrium sensilla are frequently observed in other insects on various body parts; they might represent a homoplasy. The autapomorphical characters of these sensilla (SQS, CBS, and PDS) could well serve for the confirmation of the monophyly of both subfamilies. In an earlier study the monophyly of these taxa was not questioned [30].
Generally, the Corixoidea is regarded as a taxon with several advanced characters [2,30,45], and presently a trend has been demonstrated towards changes in the type and distribution of the sensilla on the labium in comparison to other nepomorphan taxa.
The modified sensilla types (ribbon-like sensilla) are situated either in transverse bands in the Corixinae, Diaprepocoridae, and Micronectidae or without bands in the Cymatiinae. Presumably, in the first case it is a synapomorphy for the Corixidae (except the Cymatiinae), Diaprepocoridae and Micronectidae, and in the second case it is an autapomorphy for the Cymatiinae. The number of bands can be a crucial factor among the taxa and supply autapomorphical characters for these families. Currently, in each of the six species of the Corixidae, six bands have been counted, and in the Micronectidae (Micronecta quadristrigata) four bands have been found while in the Diaprepocoridae (Diaprepocoris zealandiae) two and a half bands have been observed. As for other members of the Corixidae, Lo and Acton [14] pointed out six bands in Cenocorixa bifida while in the same species Jarial [13] pointed out seven bands.
The presence of chaetica sensilla on the lateral side of the labium represents the synapomorphic character for these taxa. It is probable that these sensilla (i.e., ribbon-like sensilla) evolved from a more plesiomorphous peg-like sensillum or cupola-like sensilla of belostomatids. On the other hand, the sensilla of corixids are more similar to the paddle-like sensilla of the Ranatrinae, and a transformation of the characters directed from nepids to corixids could be indicated. A strong modification of the shape of the labium, diet type [2,11,45], modification of the food pump structures [33], and presently modification of the shape and distribution pattern of the sensilla of corixids rather lead to a conclusion that this group belongs to the advanced evolutionary line. These assumptions contradict those of Hua et al. [31], who interpreted the Corixidae as the basal taxon. The Ochteridae have retained the plesiomorphic set of characters of chaetica sensilla but they have a clearly different distributional pattern of the cupola and peg sensilla: they are arranged in six regular rows along the last segment of the labium, which can be treated as their apomorphic feature with respect to the basal morphological plane of the sensilla. The cupola and peg sensilla in the Gelastocoridae have the same pattern as in the Ochteridae, which indicates a possible synapomorphy. An interesting process of differentiation of the mechanosensilla can be seen in the Gelastocoridae. In the Gelastocorinae the two new types of sensilla (FRS, HLS) could be considered as autapomorphies, while in the Nerthrinae the chaetic sensillum with a bisected tip (CHB) has the autapomorphical character. Apart from that, the peculiar shape of the star-like sensillum (divided into four plates), which has evolved only in the Aphelocheiridae, is regarded as an autapomorphy. Further changes regarding the shape of mechanosensilla have to be postulated within subfamilies of the Naucoridae. In the Cryphocricinae, Limnocorinae, and Naucorinae, the multilobe sensilla on the IV segment are present and have been identified as synapomorphy for them, in contrast to the Cheirochelinae and Laccocorinae with the peg sensilla on the IV segment (plesiomorphic condition). The relationship of these taxa is unclear in this arrangement [26], and further discussion in this area appears premature. In the opinion of Hebsgaard et al. [30], the Naucoridae is a monophyletic family. This hypothesis probably cannot be supported by synapomorphic characters found for the two groups: the first comprising the Cheirochelinae and Laccocorinae and the second comprising the remaining subfamilies: the Cryphocricinae, Limnocorinae, and Naucorinae. The chaetic sensillum with a bisected tip (CHB) in the Nerthrinae possibly provides support to the star-like sensilla in the Aphelocheiridae, with the tip deeply divided into four narrow lobes, which in turn may be a prerequisite for the further transformation into the multilobe-like sensilla of the Cryphocricinae, Limnocorinae, and Naucorinae.
The peg sensilla are common in a few taxa of the Nepomorpha, such as the Belostomatidae, Ochteridae, and Gelastocoridae, and in the Corixoidea. Assuming that the peg sensilla and cupola sensilla are present on the ground plan of nepomorphans in basal families, the loss of these structures which can be observed within the Pleidae, Helotrephidae, and Notonectidae points out synapomorphies for these taxa. Pleoidea (Pleidae + Heloterphidae) points to the origins of this structure in these taxa. Probably, this character can be estimated as synapomorphy for this group of families. In fact, chaetica sensilla have apparently evolved at least twice within the Nepomorpha, on the I, II, and III segment in several groups (Belostomatidae, Nepidae, Corixidae, Diaprepocoridae, Micronectidae, Ochteridae, Gelastocoridae, Aphelocheiridae, and Naucoridae) and on the IV segment in representatives of the Pleidae, Helotrephidae, and Notonectidae. Previous studies strongly supported the view of separated superfamilies Notonectoidea (including one family Notonectidae) and Pleoidea (including the Pleidae and Heloterphidae), recognized by China [45], Popov [2], Rieger [33], and Hebsgaard et al. [30]. The presently reported new synapomorphy of these three taxa rather supports the existence of the "superfamily" Notonectoidea (Notonectidae + Pleoidea (Pleidae + Helotrephidae) which is similar to what was proposed by Mahner [32]. sensilla (TRS) in the nepomorphan labium. They are as follows: the first, TRS on the fourth segment (in dorsal and ventral sides as well as on the lateral side), is restricted to the Nepidae (autapomorphy); the second in dorsal and ventral sides is restricted in the four families (Belostomatidae, Notonectidae, Pleidae, and Helotrephidae) and represents a plesiomorphic character; the third, TRS on the fourth segment only in the ventral position (Ochteridae, Gelastocoridae, and Aphelocheiridae) represents synapomorphies for these taxa; the fourth, TRS on the third segment in the dorsal position, is a novelty and is an autapomorphy for the Naucoridae; similarly, the absence of the TRS in the Corixoidea could be an autapomorphy for this taxon.
A general separation of the families in the light of the types of distribution of the trichoid sensilla is similar to their systematic status. The analysis of the trichoid sensilla in particular families or subfamilies has shown that the number of these sensilla is a differentiating factor for these taxa. In the Belostomatidae, numerous trichoid sensilla have been observed (3-8 dorsal, 11-12 ventral pairs) which is similar to some of the Naucoridae (4-12 dorsal and 4-12 ventral pairs), and there is a tendency for the reduction in their number in the remaining groups, for example, in the Nepidae (4-6 dorsal and 4-6 ventral pairs and lateral 4 pairs), Notonectidae (2-9 dorsal, 1-5 ventral pairs), and Pleidae and Helotrephidae (1-3 dorsal and 1-3 ventral pairs), as well as in the Ochteridae, Gelastocoridae and Aphelocheiridae (2 ventral pairs).
A significant loss of the trichoid sensilla in the Ochteridae, Gelastocoridae, and Aphelocheiridae could, therefore, fit in with their common evolutionary trend. The Ochteridae and Gelastocoridae-neither of which has trichoidea sensilla at the dorsal side-have long been thought to be closely 36 The Scientific World Journal  [4,8].
Mechanosensilla vary greatly in size and form and are shaped as thin hairs, chaetica, trichodea, trichobothria scale, filament, and peg. The shafts of sensilla protrude from the surface of cuticle, and their base is attached by an articulation membrane forming the flexible socket. The hair is usually drawn to a sharp tip and exteriorly may bear cuticular sculpturings such as grooves or spicules. Mechanosensilla have a wall-nonpore except the molting pore near the base [6,8]. (B) Contact-chemoreceptive sensilla (bimodal sensilla) Sensillum has 3-10 neurons [28]. Chemosensitive dendrites are not branched and extend to tip of cone within dendrite sheath, which also ends in tip of cone. In addition, sensillum has a mechanosensitive neuron ending at the cuticle of the cone base and a tubular body [4].
The contact-chemoreceptors are short as well as hairs or various cones characterized by presence of a single pore at or close to the tip of the projection. These sensilla are placed on the surface and equipped with an articulation in a socket. They are often wider at base and gradually tapering towards the apex. The cuticular walls of these sensilla are smooth, with the molting pore near the base [4,6]. Tp: with one terminal pore: uniporous.
The gustatory receptor can be located in a hair, papilla, basiconic, peg-, or plate-like elevations of the surface or beneath the flat areas that have a single terminal pore (TP-sensilla, uniporous). Generally, their base is sunken into inflexible sockets. The presence of the pore at the end of the sensillum shows their chemical function [6,7]. Tp: with one apical pore: uniporous.
(D) Chemoreceptive sensilla Sensillum has 3 neurons. The dendrites of the two neurons extending into lumen of peg are hygrosensitive. A third dendrite ending below the base of the peg is thermosensitive. All dendrites are surrounded by dendrite sheath [4].
Coeloconic sensilla are usually concealed in a pit of cuticle and it is without pores [6]. NP: nonpore.
Peg-in-pit sensilla (PIP): with an inflexible socket sunken in cavity. related to each other based on other characters [2,[30][31][32][33]45]. In turn, the Aphelocheiridae, albeit having the general appearance of many naucorids, they differ in some characters, particularly, the relative length of the labium. On the other hand, similar lengths of the labium are characteristic for the Ochteridae and Aphelocheiridae [9,46], and thus it seems that labial sensilla might have evolved simultaneously with the labium. Also trichoid sensilla at the third segment in the Naucoridae can have evolutionary significance; they have probably evolved independently.

Papillae and Peg-in-Pit
Sensilla. The papillae and pegin-pit sensilla can be found together only on the labial tip. The papillae sensilla (PAS1) are situated on the smooth tip in the Belostomatidae, Nepidae, and Nerthrinae (Gelastocoridae), Table 2: Detailed description of the number, shape, and distribution of the labial mechanosensilla and contact-chemoreceptive sensilla of the species representing nepomorphan taxa. Species marked with an asterisk ( * ) are illustrated. Characters of all featured species have been analyzed and compared.  and sensilla (PAS2) are situated at the folded tip in the remaining families. The labial tip of nepomorphan families shows a fairly homogeneous distribution of PAS1 and PAS2 sensilla as well as morphological similarity and identical function. At the same time, the peg-in-pit (PIP) sensillum can be observed in lateral position in the Belostomatidae and Nepidae or in the central position on the labial tip in most of the remaining taxa. Another aspect of this sensillum (PIP) is the possibility of its presence in all taxa. On the basis of the present documentation this type of sensillum does not occur in the ochterids, gelastocorids, and aphelocheirids. It is possible that it could be hidden in the folded labial tip in these groups and therefore has not been identified in them. Due to the presence of this type of sensillum in most representatives of nepomorphans it can be regarded as putative symplesiomorphy for them.
As far as other heteropterans are concerned, the papillae sensilla do not occur in the Gerromorpha [Brożek and Zettel, in prep], Pentatomomorpha [16][17][18][19], and the Cimicomorpha [15,25], but very similar short peg-like sensilla and basiconiclike sensilla have been reported to exist on their labial tips. Furthermore, in the above-mentioned groups the peg-inpit sensillum has been observed. Assuming the conservative approach to these observations I consider that the papillae sensilla (PAS1 and PAS2) are homologous in all nepomorphans. According to the currently accepted phylogeny of the group [30], the PAS1 papillae sensilla represent, therefore, the plesiomorphic state (Belostomatidae + Nepidae), from which at least new apomorphically-shaped PAS2 sensilla have evolved. The presence of the PAS1 can be considered as a possible symplesiomorphy for the clade Belostomatidae + Nepidae and for the Nerthrinae, but the PSA2 are a synapomorphy for the rest of the Nepomorpha. Assuming that the Gerromorpha is the sister group of the Nepomorpha [36] and peg-in-pit sensilla (PIP) are homologous in both infrorders, as well as in the remaining advanced infraorders of the Cimicomorpha (e.g., in the Peiratinae and Triatominae), the presence of the PIP is probably a symplesiomorphy for the Neoheteroptera and Panheteroptera. However, more morphological studies of the heteropteran labial sensilla in all these groups are needed before positive conclusions can be reached.

The Labial Sensilla and Their Function
4.4.1. Mechanosensilla. The sensilla described in the present study are referred to as ribbon-like sensilla in the corixids while in the works by Benwitz [10], Lo and Acton [14], and Jarial [13] are referred to as peg sensilla. The ribbon-like sensilla are classified as mechanosensilla (they lack pores and are sunken in the socket) and evidence of this morphological similarity has also been found in the case of peg sensilla [14]. The ultrastructure of labial sensilla (peg) in the Cenocorixa bifida does not allow, according to Lo and Acton [14], the identification of their exact function. The modified ciliary structures observed in the dendrites are known to occur in many different receptors (photoreceptors, mechanoreceptors, and chemoreceptors). In several, out of over 2000, sensilla the cuticle is permeable to a solution of crystal violet, which makes it possible that these sensilla have a chemoreceptive function. In the case of most peg sensilla, the function is not known. Another possible function of the transverse bands of sensilla on the labium might be associated with osmotic and ionic regulations [14]. According to Jarial [13], the semicircular groove with the pores and numerous small pores on the transverse bands in the Cenocorixa bifida play a role in the uptake of water as well as ions from the surrounding medium, and the labium is engaged in the active transport of ions from the medium into the haemolymph.
In the present study the species of the Corixidae (except for the Cymatiinae), Micronectidae, and Diaprepocoridae have been observed to have the transverse bands with the semicircular grooves and pores and the set of sensory organs identical with that described by Lo and Acton [14] and Jarial [13]. At the same time, in the Cymatiinae the semicircular grooves with the pores have not been observed, and their set of sensory organs is slightly different. Among the ribbonlike sensilla the typical peg sensilla are present, and probably most of them can be an associated with osmotic and ionic regulation.
It is reasonable to assume that most of the different types of the mechanosensilla occurring on the labium in other nepomorphans (Table 1(A)), although they are not equipped with pores, may also have the ability to permeate water as well as ions from the surrounding medium.
It is surprising that many forms of various mechnosensilla of water bugs are presently being discovered while in some terrestial groups of bugs there seems to be less diversity with respect to the types of mechanosensilla (three to five types of chaetic sensilla) on the labium [15,25,43]. It is rather obvious that the numerous chetica sensilla play mainly a tactile function, whereas the remaining different types of mechanosensilla in the water bugs can also have the osmoregulatory function.
With respect to their position, the trichoid setae (prioprereceptive sensilla) play a role in monitoring the position of the segments of the labium. They are commonly found in insects around joints, where they assist in prioprereception just as the campaniformia sensilla [4].

Gustative and Contact Function on the Labial Tip.
In nepomorphans, the main group of the sensilla at the tip of the labium is that of the uniporous papilla sensilla (PAS1, PAS2) (Table 1(C)). The presence of only two similar shapes of these sensilla on the labium is probably linked to the detection limit of the number of chemical stimuli through close and direct contact of the predator with its victim.
Sensilla of a similar shape but more flattened have been found in the Gerromorpha (plate sensilla: triangular and oval ones) as well as dome-shaped sensilla, which represent the group of gustatory sensilla [Brożek and Zettel, in prep]. The presence of gustative peg sensilla has been observed in other studied heteropteran taxa of the Cimicomorpha (Reduviidae), and typical basiconic sensilla functioning as the gustative and contact-chemoreceptive sensilla have been observed in several species of the Pentatomomorpha. Moreover, the contact-chemoreceptive sensilla in many insects are represented by various forms of bristles, spots, cones, pits, and domes. Each of these has one external pore and is innervated by neurons with features characteristic of chemoand mechanoreceptors [8]. Ultrastructural studies show that sometimes a mechanoreceptive dendrite may be associated with the sensilla that function as contact-chemoreceptive sensilla [7] (Table 1(B)). Such sensilla, with a terminal pore and a flexible socket and bent at the base of the stem, have been observed during our study; they should be regarded as mechano-chemoreceptive ones. Presently, it is certain that the trichoid sensilla have a terminal pore (Figure 4(a)) and are embedded in a flexible socket.

The Labium and the Thermohygroreceptive Function.
As for the peg-in-pit sensilla (PIP), their function has not been explicitly identified yet, however, drawing a conclusion from their presence on the labial tip (or another surface of the labium) it can be suggested that their function is possibly thermohygroreceptive (Table 1(D)). They are similar to the peg-no-pore sensilla [47] generally associated with thermohygr-perception, having a triad of neurons for cold, dry, and moist detection and described as occurring in many other insect orders [48][49][50][51][52][53][54]. Generally, these sensilla are present in low numbers and are distributed mainly on both lateral faces of the antennomeres, and only rarely on other parts of insect bodies. However, this type possibly occurs also on the labium. A confirmation of this has been found in terrestrial heteropterans and auchenorrhynchans, where the thermohygroreceptors of the peg-in-pit sensilla are spread over both the labial segments [3,15,25] and the antennae [6]. The geromorphan families seem to be morphologically similar to the nepomorphan ones regarding the labial structures mentioned above [Brożek and Zettel, in prep]. Moreover, Shoonhoven and Henstra [21] have provided further evidence that the twelve sensilla basiconica on the tip of the labium of Dysdercus (Pyrrhocoridae) are contact chemoreceptive and-in addition to their apparent role in sampling the substrate for food-they could also function as thermohygroreceptives because the bugs imbibe liquid food. In the water habitat, the thermohygroreceptive sensillum on the labium of the nepomorphans can be assumed to play some role also in feeding because this type of sensilla is more numerous on the antennae and used in order to control humidity and temperature during flights to other water bodies as well as during changes of temperature in a particular water body.

Phylogenetic Implications and Conclusions
(1) On the labium of water bugs there are more or less numerous sensilla of various shapes and sizes, classified as chemosensilla and mechanosensilla. According to the morphological characteristics of the labial sensilla it appears that they can provide the water bugs with information about tactile and gustative stimuli when they come in contact with a victim. Moreover, the types of these sensilla and their distribution on the labium also provide specific valuable systematic information regarding the subfamilies or families and allow insights into the complexity of character evolution.
(2) The present comparative morphological study of the labial sensilla characters may enrich the scope of research focusing on the phylogeny of the Nepomorpha. Two latest hypotheses on infraorder families relationships that have been presented by Hebsgaard et al. [30] and Hua et al. [31] are in conflict regarding crucial points; that is, they are at odds with regard to recognition of the basal taxon in the phylogeny stem, as well as the position of the Pleidae. Nonetheless, a future comprehensive cladistic analysis using a range of morphological complexes and new characters of the labial sensilla will shed light on the evolution of the Nepomorpha. However, some preliminary phylogenetical remarks seem justified even at this point.
(3) The greater part of the labium surface of water bugs is covered by "hair" layers. Nevertheless, several types of other mechanosensilla presently recognized in the taxa of the Nepomorpha might represent an evolutionary novelty. Presently, it is postulated that the cupola and peg sensilla are plesiomorphic features of the Belostomatidae, whereas the paddle-like sensillum in the Ranatrinae, the squamiform sensillum in the Nepinae, the clubbed-like sensillum in the Gelastocorinae, the chaetica sensillum with a bisected tip in the Nerthrinae, the star-like sensillum in the Aphelocheiridae, and finally the multilobe sensillum in some of the Naucoridae are an autapomorphy for each one of them, whereas the ribbon-like sensillum is synapomorphy for the Corixidae, Micronectidae, and Diaprepocoridae.
(4) Substantial differences in the mechanosensilla set have been found between the subfamilies Gelastocorinae and Nerthrinae (Gelastocoridae). In the present study two autapomorphies (FRS, HLS) for the Gelastocorinae as well as two autapomorphies (CHB, COS) for the Nerthrinae have been evidenced. Will this difference have an influence on the phylogenetic value and rank of these taxa in the future?
(5) Nevertheless, the short trichoid sensilla placed ventrally have been reported in only three taxa (Gelastocoridae, Ochteridae, and Aphelocheiridae), and this structure might represent an evolutionary novelty for them. There is evidence pointing to a close relationship between the Gelastocoridae and Ochteridae which, taken together, have formed the Ochteroidea, but the Aphelocheiridae are rather distal in relationship from those families and have formed the Aphelocheiroidea together with the Potamocoridae [30]. (6) The presence of trichoid sensilla on the third segment is limited only to the subfamilies of the Naucoridae, and it is a satisfactory score (one synapomorphy)