Phasmatocoris ecuadorensis, Gil-Santana, 2021

Gil-Santana, Hélcio R., 2021, A new species of Phasmatocoris Breddin, 1904 (Hemiptera: Heteroptera: Reduviidae: Emesinae) from Ecuador, with taxonomic notes and an updated key of the genus, Revista Chilena de Entomología (Rev. Chil. Entomol.) 47 (3), pp. 573-589 : 575-583

publication ID

https://doi.org/ 10.35249/rche.47.3.21.16

publication LSID

lsid:zoobank.org:pub:9D52A173-4792-4A6A-9CDF-7B1EF5F5C38F

persistent identifier

https://treatment.plazi.org/id/685687D7-FFC7-C376-FE5F-FEE6FF6FFE0E

treatment provided by

Felipe

scientific name

Phasmatocoris ecuadorensis
status

sp. nov.

Phasmatocoris ecuadorensis sp. nov.

( Figs. 1-35 View Figures 1-6 View Figures 7-12 View Figures 13-17 View Figures 18-23 View Figures 24-27 View Figures 28-31 View Figures 32-35 )

Type material. Holotype ♂ [ MNRJ], Ecuador, Pichincha, 18 / V / 1997, Sanchez, P. leg.

Etymology. The specific epithet ecuadorensis is derived from Ecuador, the South American country in which the species was found with the Latin adjectival suffix “-ensis”, meaning “pertaining to” or “originating in”.

Diagnosis. The male most closely resembles that of Ph. papei Gil-Santana, 2018 . The two species can be readily separated by the differences stated in the key below and additionally by the following characteristics of their phalli: 1) basal plate struts (bp) relatively shorter and enlarged, racket-shaped, basal half with subparallel margins, distal half suboval; narrowly to somewhat divided at basal portion and largely divided at apical portion; apical extremities rounded and somewhat asymmetrical in Ph. papei and elongated, generally narrow with basal portion largely divided in two branches, somewhat enlarged in the median portion and even narrower at distal half, which has most of its central portion deepened, bordered by narrow margins, and convergent at the apical extremity in Ph. ecuadorensis n. sp. ( Figs. 26 View Figures 24-27 , 29-30 View Figures 28-31 ); 2) The short sclerotization of dorsal wall of phallosoma (sdw) located ventrally and dorsally in relation to the apical portion of basal plate struts in Ph. papei and Ph. ecuadorensis sp. nov., respectively ( Figs. 26 View Figures 24-27 , 28, 30 View Figures 28-31 ); 3) Ventral median sclerotization of dorsal wall of phallosoma (sdw) elongated, shortly divided at extreme base, narrowed at approximately middle portion in Ph. ecuadorensis sp. nov. ( Figs. 25, 27 View Figures 24-27 , 28 View Figures 28-31 , 35 View Figures 32-35 ) and becoming divided in apical third, forming a subsquared, somewhat larger and asymmetrical apical flat process in Ph. papei ; 4) Three and only two processes of endosoma in Ph. papei and Ph. ecuadorensis sp. nov., respectively; 5) Dorsal process of endosoma (dps) shorter in P. papei , reaching approximately at level of the middle portion of basal plate struts, while it is more elongated in Ph. ecuadorensis sp. nov., reaching short of the apex of basal plate struts ( Figs. 26-28 View Figures 24-27 View Figures 28-31 ); 6) Basoventral moderately large process of endosoma (bv) flat, with a short narrow striate basomedian portion, surrounded by curved layers, which are distally connected with a pair of flat, narrow laminar portions in Ph. ecuadorensis sp. nov. ( Fig. 34 View Figures 32-35 ), and its equivalent in Ph. papei (“large process of endosoma”, according to Gil-Santana 2018a) with a sclerotized elongated core surrounded by filamentous and membranous layers, enlarged at base and somewhat narrowed and asymmetrical towards apical third, in which at one side only there is a somewhat curved sclerotized band.

Description. Measurements: (holotype, in mm): total length: to tip of abdomen: 17.5; to tip of forewings: 16.6. Head (excluding neck): length: 1.8; length of anteocular portion: 0.7; length of postocular portion: 0.4; width across eyes: 1.4; interocular distance between eyes (synthlipsis): 0.6; width of eye: 0.3; length of eye: 0.5; lengths of antennal segments: I: 11.5; II: 10.2.; III: 1.0; IV: 3.3; lengths of labial segments: II [first visible]: 0.3; III: 0.5; IV: 1.1. Thorax: pronotum: fore lobe: length: 2.2; maximum width: 1.0; hind lobe: length: 1.9; maximum width (at posterior margin): 1.6; length of forewing: 10.9; length of hind wing: 9.8; fore legs: length of coxa: 4.4; length of femur: 6.0; length of tibia: 2.8; length of tarsus: 0.9; middle legs: length of femur: 11.5; length of tibia: 15.5; length of tarsus: 0.8; hind legs: length of femur: 15.1; length of tibia: 24.0; length of tarsus: 0.8. Abdomen: length: 10.8; maximum width: 1.1. Coloration: general coloration dark brownish to blackish ( Figs. 1-6 View Figures 1-6 ). Head ( Figs. 4-5 View Figures 1-6 ): apices of antenniferous tubercles, extreme base of first antennal segment, and labrum pale; last antennal segment basally dark, becoming progressively paler towards apex; small median depressed area present immediately anteriad of transversal sulcus deep black; labium somewhat paler at the junction between segment III (second visible) and IV and at tip of the latter; area just posterior to the eyes reddish brown. Thorax: angles of collar of fore lobe of pronotum dark reddish ( Figs. 4, 6 View Figures 1-6 ); anterolateral angles of hind lobe of pronotum with a subtriangular dark yellowish spot, larger anteriorly ( Fig. 3 View Figures 1-6 ). Fore legs: generally brownish, trochanters darker; fore femora paler at medial surface, between the isolated seta and the remaining setae of the anteroventral series, its approximately distal half darker, with a subdistal pale annulus about as long as the width of the segment ( Figs. 3 View Figures 1-6 , 9 View Figures 7-12 ); base of tibiae darker; tarsi slightly paler ( Figs. 10-11 View Figures 7-12 ). Middle and hind legs: femora brownish black, becoming darker, blackish towards apices; hind femora with subapical narrow yellowish spots, on lateral and dorsal surfaces, not forming a complete annulus ( Fig. 12 View Figures 7-12 ); tibiae generally blackish, with a pale spot at ventral surface of extreme base and paler at distal portion; tarsi pale. Forewing ( Fig. 13 View Figures 13-17 ): generally dark brown; basal third of basal cell pale whitish; inner margin of pterostigma with reddish tinge, except at its apex; portion of vein M which runs at the middle third of the wing and Pcu+1A paler; adjacent portions of mentioned part of vein M, more extensively on outer margin, even paler, whitish at the level in which this vein encloses basal cell and basal portion of discal cell; most portions of Cu and M enclosing inner and distal portions of discal cell pale whitish, with adjacent membrane with the same color, which extends posteriorly in the area adjacent to the pterostigma; an additional pale linear marking between discal cell and inner margin of wing; a distal curved vein marked with pale coloration at its median portion. Hind wings hyaline, veins somewhat and variably darkened. Abdomen: distal half of tergite II, tergites III-VI and basal half of VII pale brownish; tongue-shaped prolongation of tergite VII dark brownish; connexivum slightly darkened, connexival segments III-VII with small ill-defined basal pale markings; spiracles of the sternites III-VII and the area surrounding them paler; lateral and basolateral portions of sternite VIII and pygophore, respectively, paler. Vestiture: body integument generally covered with a pubescence formed by numerous very short slender adpressed setae and variably scattered longer setae. Head: mostly covered by a pubescence formed by adpressed short thin pale setae, with scattered longer setae on lateral region, clypeus and first visible labial segment. Labial segments III and IV mostly glabrous; the former and the basal and apical portions of the latter with a few scattered straight erect very short pale setae; additionally, a pair of more elongated, curved, pale yellowish setae at apical portion of the segment IV. A group of stouter, moderately longer, dark setae beside anteroventral portion of eye. Glabrous areas on head: transverse sulcus, the portion just anterior to it, including the small median depressed area, and a pair of submedian slightly divergent thin bands running from midportion of transverse sulcus to a point near medial margin of antenniferous tubercles. Antenna generally covered with thin dark setae, longer on the first segment and whitish pale on the last segment, except on basal portion where they are pale brownish. Thorax: fore lobe of pronotum with sparse, short, adpressed, thin pale setae on dorsal and lateral portions; longer thin setae on lobe of acetabula and ventral surface of basal prominent portion of prosternum; hind lobe almost glabrous, with sparse somewhat curved setae on distal portion; meso- and metapleura, pro-, meso- and metasterna covered by a somewhat sparse pubescence formed by short, thin, adpressed small setae; lateral portion of mesosternum glabrous. Legs covered by numerous short to somewhat longer thin setae, pale or dark, similar to the coloration of integument which they are inserted on. Armature of ventral surface of fore femora only with slender spine-like setae in two series, posteroventral and anteroventral, apically transformed into short teeth; anteroventral series interrupted at base, not connected to posteroventral series, one isolated seta basal to interruption ( Fig. 9 View Figures 7-12 ); distance between this latter and first seta of series 0.5 mm; distance from base of fore femur to insertion of first spiniform seta of anteroventral series 2.9 mm, and from apex of fore trochanter 2.5 mm. Distance from base of fore femur to insertion of first spiniform seta in posteroventral series, approximately twice longer than length of fore tarsus, 2.0 mm, and from apex of fore trochanter, 1.6 mm. Left femur with an additional [broken] seta between the base of the segment and the posteroventral series ( Fig. 9 View Figures 7-12 ); respective distances between this seta and first seta in posteroventral series, apex of trochanter and base of femur (in mm): 0.6 / 1.0 / 1.5. Longer setae in posteroventral series, with length approximately as long as the value of maximum width of fore femur. Fore tibiae ( Figs. 10-11 View Figures 7-12 ) with a cluster of stiff obliquely inclined pale to golden setae on approximately distal half, dorsally, more numerous just basad to depressed area of this portion; numerous straight short setae close beside medial series of denticles ventrally; inner surface on approximately distal fourth, with dense short adpressed golden pubescence and a subapical comb; apex with a dense cluster of golden stiff setae ventrally. Wings glabrous.

Abdomen generally covered by a pubescence formed by short, thin, adpressed small setae and scattered longer setae. Pygophore more densely setose. Structure: Integument generally moderately shiny. Head elongated, approximately 1.2 times as long as wide across eyes; anteocular portion longer than postocular ( Figs. 4-5 View Figures 1-6 ); transversal (interocular) sulcus deep, situated at level of distal portion of middle third of eyes ( Fig. 4 View Figures 1-6 ); a small median depressed area present immediately anteriad of it; distance from apex of antenniferous tubercle to anterior border of eye in lateral view (0.45 mm) slightly shorter than length of eye (0.5 mm); eyes prominent, projecting laterally, subcircular in dorsal view, reaching dorsal outline of head at interocular sulcus and ventral margin of head ( Figs. 4-5 View Figures 1-6 ). Antennal segments progressively thinner, very slender; segment IV with apex triangular. Labial segment III (second visible) thickest, apex proximal to the level of anterior margin of eye; segment IV longest. Thorax: fore lobe of pronotum approximately 1.15 times longer than hind lobe, subrectangular in dorsal view ( Figs. 2, 6 View Figures 1-6 ); anterior projections of collar rounded and prominent ( Fig. 4 View Figures 1-6 ); integument dull, rugose and transversely striated, dorsally and laterally; with a welldefined longitudinal medial shallow furrow, with rugose integument; transverse interlobar sulcus deep, thin and curved ( Fig. 6 View Figures 1-6 ). Hind lobe of pronotum shorter and larger than fore lobe; somewhat enlarged towards apical margin; integument mostly smooth, shiny, with faint transversal striations more numerous at distal portion, with a wide, distinct longitudinal shallow depression, enlarged at its median portion, not reaching basal and distal portions, with rugose integument ( Figs. 2, 6 View Figures 1-6 ); posterior margin with numerous longitudinal thin shallow ridges, forming a wrinkled integument; humeral angles with elevated rounded tubercles. Lateral margins of stridulitrum conspicuously protuberant. Scutellum moderately elevated, with a small median pointed horizontal prominence at its tip ( Figs. 7-8 View Figures 7-12 ). Metanotum with a short, pointed, horizontally directed backwards prominence ( Figs. 7-8 View Figures 7-12 ). Fore coxae and fore femora elongated, latter somewhat broadened at submedian basal portion ( Fig. 3 View Figures 1-6 ); fore tibia approximately half as long as fore femora, dorsally depressed approximately at basal portion of distal half, ventrally with a single series of hook-like denticles, which are absent at basal portion and extreme apex; inner surface on distal quarter somewhat flattened ( Figs. 10-11 View Figures 7-12 ). Mid and hind femora and tibiae very long and slender. Tarsi three-segmented, slender. Forewings approaching apex of abdomen and apex of genitalia by approximately 0.4 mm and 1.0 mm, respectively; pygophore and about posterior half of tongue-shaped prolongation of last tergite exposed on dorsal view ( Fig. 2 View Figures 1-6 ); subbasal cell longer than basal cell; subbasal and discal cells clearly separated by basal cell ( Figs. 13-14 View Figures 13-17 ). Hind wings reaching distal portion of tergite VI; venation as in Fig. 15 View Figures 13-17 . Abdomen: first tergite subrectangular, elevated in relation to the following tergites, its spiracle beside the anterolateral margin; segment II narrow; segments III–V progressively slightly widened towards apex; segment VI slightly narrowed towards apex; segment VII more narrowed towards apex, dorsally with a tongue-shaped prolongation posteriorly, which is rounded apically, somewhat wider at base, ending at level of approximately middle third of pygophore ( Figs. 16-17 View Figures 13-17 ). Connexival segments simple, straight. Sternites I-VI with a median longitudinal thin and shallow carina. Eight sternite slightly enlarged toward apex, with posterior margin somewhat curved at ventral and laterosuperior portions, the latter, just below the spiracle ( Figs. 17-18 View Figures 13-17 View Figures 18-23 ). Male genitalia ( Figs. 16-35 View Figures 13-17 View Figures 18-23 View Figures 24-27 View Figures 28-31 View Figures 32-35 ): pygophore subrectangular in dorsal and ventral views ( Figs. 19-20 View Figures 18-23 ); in dorsal view: between anterior and posterior genital openings, a narrow dorsal (transverse) almost straight bridge (br) ( Fig. 19 View Figures 18-23 ), proctiger (pc) subsquared to subrectangular, somewhat enlarged towards apex ( Fig. 19 View Figures 18-23 ); process of pygophore (pp) spine-like in dorsal, ventral and posterior views ( Figs. 19-21 View Figures 18-23 ), curved in lateral view ( Fig. 23 View Figures 18-23 ). Parameres symmetrical ( Figs. 19-21 View Figures 18-23 ), curved, with apical half enlarged, suboval in shape ( Fig. 24 View Figures 24-27 ); outer surface densely setose, not impressed on disc ( Fig. 24A View Figures 24-27 ); inner surface less setose, with a pair of small pointed processes at its tip ( Fig. 24B View Figures 24-27 ). Phallus ( Figs. 25-27 View Figures 24-27 ): articulatory apparatus with basal arms (ba) shorter than phallosoma, divergent, connected by a short and narrow basal bridge ( Figs. 25-27 View Figures 24-27 ); basal plate struts (bp) ( Figs. 25-26 View Figures 24-27 , 29-30 View Figures 28-31 ) elongated, generally narrow, strongly double curved in lateral view, in dorsal view: basal portion largely divided into two branches, more enlarged in the median portion and even narrower at distal half, the latter with its central portion deepened, bordered by narrow margins; apical extremity convergent, their sides somewhat asymmetrical, and covered by the basal portion of the sclerotization of the dorsal wall of phallosoma (sdw). The latter, short, subsquared, slightly asymmetrical, and located dorsally and partially over to the apical portion of basal plate struts ( Figs. 25-26 View Figures 24-27 , 28, 30 View Figures 28-31 ). An elongated median sclerotization of the ventral wall of phallosoma (svw) ( Figs. 25, 27 View Figures 24-27 , 28 View Figures 28-31 , 35 View Figures 32-35 ), which is shortly divided at extreme base and narrowed at approximately middle portion with apical margin continuous with apex of dorsal membranous wall (svwd) ( Figs. 25-26 View Figures 24-27 , 28 View Figures 28-31 ); Endosoma wall smooth. Endosoma with two processes: 1) a large, elongated, flat, subtriangular, somewhat sclerotized dorsal process (dps), with asymmetrically curved margins, enlarged at basal portion, which has a pair of narrow lateral branches; it is covered by a spiny membrane at approximately its basal third, and by several small spines at lateral portions of approximately its distal half, except at the apex, which is less sclerotized, rounded and smooth and is located short of apical portion of the dorsal phallothecal plate ( Figs. 25-28, 31-33 View Figures 24-27 View Figures 28-31 View Figures 32-35 ); 2) a basoventral moderately large process (bv) with a flat short narrow striate basomedian portion, surrounded by curved layers, which are distally connected with a pair of flat, narrow laminar portions ( Figs. 25, 27 View Figures 24-27 , 34 View Figures 32-35 ).

Distribution. Ecuador.

Comments. The inclusion of Ph. ecuadorensis sp. nov. in Phasmatocoris is in accordance with the characteristics assigned to this genus by Wygodzinsky (1966), Pape (2013) and Gil-Santana (2015). In this matter, it is noteworthy that Wygodzinsky (1966) argued that Phasmatocoris was distinguished from all other genera of Emesini by the considerably asymmetrical phallus. The asymmetry would often be perceptible in the phallosoma, especially in the shape of the basal plate struts and the overlying dorsal sclerotization of the phallosoma wall. The greatest degree of asymmetry, however, was found in the endosoma, especially on its apical portion, while the processes of endosoma are slightly to very strongly asymmetrical, varied in shape and number ( Wygodzinsky 1966). However, the phallic structures of Ph. ecuadorensis sp. nov. are mostly symmetrical, with slight asymmetry in the apical portion of basal plate struts (bp) ( Figs. 26 View Figures 24-27 , 30 View Figures 28-31 ) and the sclerotization of dorsal wall of phallosoma (sdw) ( Figs. 26 View Figures 24-27 , 30 View Figures 28-31 ), albeit somewhat more prominent in this matter are the asymmetrically curved margins of the dorsal large process of endosoma (dps) ( Figs. 31-33 View Figures 28-31 View Figures 32-35 ). On the other hand, in other five species of Phasmatocoris, Gil-Santana et al. (2007) and Gil-Santana (2015, 2018a) found a considerable range in the degree of asymmetry in the phallosoma and processes of the endosoma, from quite asymmetrical to basically symmetrical or only slightly asymmetrical. Therefore, the slight asymmetry recorded in phallic structures of Ph. ecuadorensis sp. nov. is in accordance with the observations of Gil-Santana (2015, 2018a) that there is a range in the degree of the asymmetry in the phallic structures among the species of Phasmatocoris .

Phasmatocoris papei , the species which seems closer to Ph. ecuadorensis sp. nov., was recorded as presenting an overall similarity with Ph. moraballi Wygodzinsky, 1966 but also to Ph. magdalenae Wygodzinsky, 1966 and Ph. sturmi Wygodzinsky, 1966 ( Gil-Santana 2018a). These three latter species were considered as closely related by Wygodzinsky (1966), who also referred to them as “a group” of “dark, medium-sized species around [Ph.] magdalenae ”, occurring in the Amazonian region. Phasmatocoris papei and Ph.ecuadorensis sp. nov. also belong to this group, but they can be separated from the other three species by the characteristics mentioned in the following key. Additionally, the phallic structures such as the shape of basal plate struts (bp) and specially the processes of the endosoma are very different among Ph. magdalenae , Ph. sturmi , Ph. papei and Ph. ecuadorensis sp. nov. ( Wygodzinsky 1966; Gil-Santana 2018a; figs. 25-34). Yet, the processes of endosoma of Ph. magdalenae , Ph. moraballi and Ph. sturmi were recorded as strongly or clearly asymmetrical by Wygodzinsky (1966), while only a slight asymmetry was recorded in some of the structures of the endosoma of Ph. papei ( Gil-Santana 2018a) , similarly to Ph. ecuadorensis sp. nov., with the exception of the more asymmetrically curved margins of the dorsal large process of endosoma (dps) ( Figs. 31-33 View Figures 28-31 View Figures 32-35 ). On the other hand, while the sclerotization of the ventral wall of phallosoma and the shape of the basal plate struts of Ph. papei seemed to be similar to those of Ph. praecellens ( Gil-Santana 2018a) (see below), the sclerotization of the ventral wall of phallosoma of Ph. ecuadorensis sp. nov. is partially similar to that of Ph. praecellens ( Wygodzinsky 1966: fig. 86L), whereas an elongated, narrow basal plate struts, as found in Ph. ecuadorensis sp. nov. ( Figs. 26 View Figures 24-27 , 29-30 View Figures 28-31 ) was also recorded in Ph. borgmeieri (Wygodzinsky, 1945) ( Gil-Santana 2015: fig. 13). In the latter species, the “flat process” of endosoma, as recorded by Gil-Santana (2015: figs. 11, 14), seems to be actually a shorter sclerotization of the ventral wall of phallosoma similar to that of Ph. ecuadorensis sp. nov. ( Figs. 27 View Figures 24-27 , 35 View Figures 32-35 ). In this case, the alleged asymmetry of the two “processes” of the endosoma of Ph. borgmeieri ( Gil-Santana, 2015) would have been a misinterpretation of this latter author in which only the tubular process (his Figs. 15-16 View Figures 13-17 ) should be considered as such and, therefore, a symmetrical process of the endosoma.

In any case, the characters of the male genitalia of Ph. ecuadorensis sp. nov. reinforce Wygodzinsky´s (1966) concept of this genus, based on the particular structure of the male genitalia, as the new species shares similarities with various species in the genus, in a mixed way, despite conspicuous differences in other characters.

The depression on the dorsal surface of the fore tibiae, covered with medium-sized stiff dense setae, which was recorded in other species of Phasmatocoris ( Forero 2006; Pape 2013; Gil-Santana 2015, 2018a) and compatible with the calamistrum-like structure described by Wygodzinsky (1966) in many emesines was observed in Ph. ecuadorensis sp. nov. ( Figs. 10-11 View Figures 7-12 ) too.

MNRJ

Museu Nacional/Universidade Federal de Rio de Janeiro

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Reduviidae

Genus

Phasmatocoris

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