Cicada pauperata Fabricius, by subsequent designation of China (1938: 183).

Specimens preserved in collections usually pale yellow; whitish-yellow to greenish-yellow in life; forewing with preapical area with irregular orange transverse band or with second apical cell with distinct red spot. Head moderately to strongly produced anteriorly; coronal suture distinct, elongate, extending anteriorly beyond interocellar line; frons, in lateral view, with inferior third slightly angulate. Pronotum with lateral margins convergent anteriorly; posterior margin rectilinear. Forewing subhyaline; apex slightly expanded and obliquely truncate; with four apical cells, base of fourth approximately aligned with base of third; costal apical cell broadened posteriorly. Male terminalia with pygofer bearing basiventral lobe; without processes; subgenital plate triangular, not fused basally to its counterpart; style without preapical lobe; aedeagus with shaft short, usually with single process, rarely with pair of processes; paraphyses present, biramous, with or without processes on stalk. Female terminalia with sternite VII well produced posteriorly; pygofer well produced posteriorly; valvula I abruptly narrowed apically, with ventroapical margin somewhat sinuous and apex acute; valvula II with dorsal margin convex, teeth non-contiguous, mostly subtriangular. See systematic notes after the generic description and section 4.3 of the discussion for additional information on the identification of the genus.

Length. ♂♂ 7.4–10.8 mm; ♀♀ 8.4–10.3 mm. Head: in dorsal view, moderately to strongly produced anteriorly; median length of crown varying from 5/10 to 9/10 of interocular width and from 4/10 to 6/10 of transocular width; anterior margin generally rounded; without carina at transition from crown to face; coronal suture distinct, elongate, extending anteriorly beyond interocellar line; frontogenal suture extending onto crown and usually attaining ocellus; ocelli large or of moderate size, located approximately on imaginary line between anterior eye angles, or slightly before or slightly behind this line, each ocellus approximately equidistant between median line of crown and adjacent eye angle; antennal ledge, in dorsal view, varying from not protuberant to slightly protuberant; in lateral view, with anterior margin oblique and convex. Frons, in anterior view, convex; median area mostly smooth; muscle impressions distinct; in lateral view, inferior third slightly angulate; epistomal suture incomplete medially; clypeus, in lateral view, convex, continuing inferior contour of frons. Thorax: pronotum, in dorsal view, with width slightly greater than or approximately equal to transocular width of head; lateral margins convergent anteriorly; posterior margin rectilinear; dorsolateral carina complete, rectilinear, declivent anteriorly; disk without pubescence or punctures. Mesonotum with scutellum not transversely striate and without punctures. Forewing with membrane indistinct; veins not elevated; apex slightly expanded and obliquely truncate; with four apical cells, base of fourth approximately aligned with base of third; with three closed anteapical cells, their bases located more proximally than claval apex; costal apical cell broadened posteriorly; without anteapical plexus of veins; texture subhyaline. Hind wing with vein R₂₊₃ incomplete. Hind leg with femoral setal formula 2:1:1; first tarsomere longer than combined length of two more distal tarsomeres, with two longitudinal parallel rows of small setae on plantar surface. Coloration: head, pronotum, mesonotum, forewings, and legs of preserved specimens usually yellow (whitish-yellow to greenish-yellow in life); preapical area of each forewing with irregular orange transverse band or with distinct red spot on second apical cell. Male terminalia: pygofer, in lateral view, moderately to strongly produced posteriorly; with basiventral lobe; without processes; anteroventral margin with distinct group of microsetae. Subgenital plate, in ventral view, not fused basally to its counterpart; not extending as far posteriorly as pygofer apex. Connective, in dorsal view, usually T-shaped, rarely V-shaped; arms broad. Style, in dorsal view, without preapical lobe. Aedeagus, in lateral view, with shaft usually short and bearing single ventral process, more rarely with pair of processes or with apical digitiform projection. Paraphyses present, symmetrical or slightly asymmetrical, with or without processes on stalk. Female terminalia: sternite VII, in ventral view, well produced posteriorly; narrowing gradually towards apex. “Internal” sternite VIII, in dorsal view, usually without sclerotized areas. Pygofer, in lateral view, well produced posteriorly; posterior margin narrowly rounded to subacute; macrosetae distributed mostly on posterior half. Valvula I, in lateral view, abruptly narrowed apically, ventroapical margin somewhat sinuous, apex acute; dorsal sculptured area extending from basal portion to apex of blade, formed mostly by scale-like processes arranged in oblique lines (strigate); ventral sculptured area restricted to apical portion of blade, formed mostly by scale-like processes; base of valvula forming lobe directed anterad; ventral interlocking device located on basal third or basal half of blade. Valvula II, in lateral view, with dorsal margin convex; blade with about 45 to 60 non-contiguous, mostly subtriangular teeth; preapical prominence distinct; apex obtuse; denticles distributed on teeth and on dorsal and ventral apical portions of blade (ventral dentate apical portion longer than dorsal portion); valvula with ducts extending towards teeth and apical area. Gonoplac of the usual Cicadellinae type: in lateral view, with basal half narrow; apical half expanded, gradually narrowing towards apex; latter obtuse.

According to the results of our cladistic analysis, the genus Dasmeusa can be distinguished from other members of the Paromenia group, as well as from other sharpshooters, by a combination of the following synapomorphic traits: (1) posterior margin of pronotum rectilinear (Fig. 8A); (2) apex of forewing obliquely truncate (Fig. 8B); (3) base of fourth apical cell of forewing approximately aligned with base of third apical cell (Fig. 8B); (4) anteroventral margin of male pygofer with distinct group of microsetae (Fig. 3B) (this character state is present in all known species of the genus; however, it was not illustrated herein for all of them because the delicate setae are sometimes not adequately preserved after the preparation of specimens in 10% KOH); (5) presence of paraphyses (Fig. 8G–I).

♂ paratypes 8.8–9.2 mm (n = 2); ♀ paratype 9.6 mm; ♂♂ 8.8–9.2 mm (n = 3). Head (Figs 1A, 2A): in dorsal view, well produced anteriorly; median length of crown approximately 7/10 of interocular width and 4/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown concave; antennal ledge, in dorsal view, not protuberant. Thorax (Figs 1A, 2A) with pronotum, in dorsal view, with width slightly greater than transocular width of head. Forewing with base of fourth apical cell approximately aligned with base of third; forewing of female, in rest position, exceeding apex of ovipositor.

Head, pronotum, and mesonotum light brown; ocelli orange. Forewing pale yellow, translucid, with veins light brown, preapical area with irregular, orange transverse band. Face, lateral and ventral portions of thorax, and legs mostly light brown.

Pygofer (Fig. 2B), in lateral view, with posterior margin obliquely truncate superiorly and rounded inferiorly, apex obtuse; macrosetae distributed mostly on posterior half but some located more anteriorly. Subgenital plate (Fig. 2C), in ventral view, with basal half broad and distal half very narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 2D), in dorsal view, T-shaped; stalk carinate dorsally, subequal in length to one arm width. Style (Fig. 2D), in dorsal view, slender, elongate, extending posteriorly beyond apex of connective; apex narrow, directed ventrally, truncate. Aedeagus (Fig. 2E) symmetrical; shaft short; whole ventral margin of shaft produced into strong, slightly bifid process directed ventrally, posterior margin of process smooth; gonoduct distinct, curved, gonopore located apically. Paraphyses slightly asymmetrical, elongate, extending well beyond subgenital plate apex; stalk shorter than rami; in dorsal view (Fig. 2F), rami fused to each other along their basal halves, each bifurcate at apex; in lateral view (Fig. 2G), stalk arched dorsally, rami directed dorsally, narrower along apical half.

Terminalia with sternite VII (Fig. 2H), in ventral view, with posterior margin narrowly rounded. Pygofer (Fig. 2I), in lateral view, with posterior margin narrowly rounded; macrosetae distributed on posterior portion and extending anteriorly along ventral margin. Valvula I, in lateral view, with ventral interlocking device located on basal third of blade. Valvula II, in lateral view, with about 47 non-contiguous teeth.

French Guiana [new record] • 1 ♂: “FRENCH GUIANA: Laussat \ P3 \ 05°28′31.6″N – 053°35′07.3″W \ 30.IX.2010 \ Lamarre G. Leg”; “White sand forest \ Vitre trap (V 7)” (DZRJ) • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 14.viii.2011 \ Malaise trap \ SEAG col.” (DZRJ) • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 09.viii.2011 \ window trap \ SEAG col.” (MNRJ) • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 24.iii.2012 \ Malaise trap \ SEAG col.” (MNRJ). Guyana • 1 ♂ paratype: “#CICA00476 \ Pentaclethra macroloba [host-plant] \ Camoudi 11-03-1997”; “Hand collecting/beating \ Station 2616 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.” (DZUP) • 1 ♂: “#CICA 076 \ Pentaclethra macroloba \ Camoudi 21/4/1997”; “Hand collecting/beating \ Station 6069 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset Coll.”; “3193” (DZUP) • 1 ♂ paratype: “#CICA00476 \ Catostemma fragrans [host-plant] \ Camoudi 11-3-1997”; “Hand collecting/beating \ Station 4126 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.” (DZUP) • 1 ♀ paratype: “#CICA00476 \ Catostemma fragrans \ Camoudi 9-05-1997”; “Hand collecting/beating \ Station 3557 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.” (DZUP) • 1 ♀ paratype: “#CICA 076 \ Catostemma fragrans \ Camoudi 24-10-1997”; “Hand collecting/beating \ Station 2476-1 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “9864” (DZUP) • 1 ♀ paratype: same data as preceding except “29-11-1996”; “Station 3273”; “2572” (DZUP) • 1 ♀ paratype: “#CICA 076 \ Eperua rubiginosa [host-plant] \ Camoudi 24-10-1997”; “Hand collecting/beating \ Station 2551-2 \ On seedlings trees”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “6916” (DZUP) • 1 ♂ paratype: “#CICA 076 \ Eperua rubiginosa \ Camoudi 16-9-1997”; “Hand collecting/beating \ Station 4184 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “9556” (DZUP) • 1 ♀ paratype: same data as preceding except “12-6-1997”; “Station 5473”; “6208” (DZUP).

Cavichioli and Chiamolera (1999) considered the habitus of D. basseti (Fig. 1A) similar to that of D. pauperata (Fig. 1H), whereas they regarded the male terminalia similar to those of D. isabellina, mainly due to the shape of the aedeagus (Figs 2E, 5E). However, D. basseti can be easily distinguished from these two species by the paraphyses (Fig. 2F, G) with the rami fused to each other along their basal halves, each one bifurcate at apex.

♂ holotype 8.4 mm; ♂ paratypes 8.0–8.4 mm (n = 3). Male holotype. Head (Figs 1B, 3A): in dorsal view, strongly produced anteriorly; median length of crown approximately 9/10 of interocular width and 4/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown slightly concave; antennal ledge, in dorsal view, slightly protuberant. Thorax (Figs 1B, 3A) with pronotum, in dorsal view, with width slightly greater than transocular width of head. Forewing with base of fourth apical cell approximately aligned with base of third; with three anteapical cells, their bases obscure.

Head, pronotum, mesonotum, and legs pale yellow. Forewing pale yellow, translucid, preapical area with irregular orange transverse band.

Pygofer (Fig. 3B), in lateral view, with posterior margin rounded; macrosetae distributed mostly on posterior half but some located more anteriorly. Subgenital plate (Fig. 3C), in ventral view, with basal half broad and distal half very narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 3D), in dorsal view, T-shaped; stalk carinate dorsally, shorter than one arm width. Style (Fig. 3D), in dorsal view, slender, extending posteriorly beyond apex of connective; narrowed apically, apex obtuse. Aedeagus (Fig. 3E) symmetrical; shaft short; ventral margin of shaft with preapical portion produced into robust process directed ventrally, posterior margin of process dentate; gonoduct distinct, gonopore located dorsoapically. Paraphyses slightly asymmetrical, articulated with apex of connective; elongate, extending well beyond subgenital plate apex; stalk longer than rami; in dorsal view (Fig. 3F), stalk long and robust, with pair of small dorsal processes on apical third and pair of small ventroapical processes; in lateral view (Fig. 3G), stalk slightly sinuous; rami slender, directed dorsally, narrowing towards apex.

The name of the new species, dinizi, refers to the biologist André Luis Diniz Ferreira, in recognition of his friendship to the first author and contribution as a skilled insect collector.

Laussat (French Guiana).

French Guiana • ♂ holotype: “French Guiana: Laussat \ P3 \ 05°28′31.6″N-053°35′07.3″W \ 12.ix.2010 \ Lamarre G. leg”; “White sand forest \ Light trap” (DZRJ). Paratypes • 2 ♂♂: same data as the holotype (DZRJ) • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 26.vi.2011 \ window trap \ SEAG col.” (MNRJ).

Dasmeusa dinizisp. nov. (Fig. 1B) is similar to D. oriximinasp. nov. (Fig. 1G). These species share many similarities in the male terminalia, especially in the aedeagus and paraphyses. However, D. dinizi can be recognized by the two pairs of small processes on the paraphyses stalk (Fig. 3G), one located dorsally at the base of the apical third and another ventrally at the apex.

♂ holotype 7.4 mm; ♂ paratype 8.0 mm; ♀ paratypes 8.4–9.3 mm (n = 3). Male holotype. Head (Figs 1C, 4A): in dorsal view, well produced anteriorly; median length of crown approximately 8/10 of interocular width and 5/10 of transocular width; anterior margin narrowly rounded; frontogenal suture extending onto crown but not attaining ocellus; ocelli of moderate size, located approximately on imaginary line between anterior eye angles; surface of crown flat; antennal ledge, in dorsal view, not protuberant. Thorax (Figs 1C, 4A) with pronotum, in dorsal view, with width approximately equal to transocular width of head; lateral margins slightly convergent anteriorly. Forewing with base of fourth apical cell approximately aligned with base of third.

Head, pronotum, and mesonotum pale yellow. Forewing pale yellow, second apical cell with distinct red spot.

Pygofer (Fig. 4B), in lateral view, well produced posteriorly; posterior margin narrowly rounded; macrosetae (most of them very large) distributed on posterior half but some located more anteriorly. Subgenital plate (Fig. 4C), in ventral view, with basal half broad and distal half very narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 4D), in dorsal view, V-shaped; stalk not carinate dorsally, much longer than one arm width. Style (Fig. 4D), in dorsal view, slender, elongate, not extending posteriorly beyond apex of connective; slightly narrowed apically, apex obtuse. Aedeagus symmetrical (Fig. 4E); in lateral view, shaft elongate, ventral margin with dentiform process at basal half and elongate process at apex; gonoduct distinct, gonopore located apically. Paraphyses, in dorsal view (Fig. 4F), slightly asymmetrical; elongate, extending well beyond subgenital plate apex; stalk much shorter than rami; in lateral view (Fig. 4G), rami with apexes slightly directed upwards.

Sternite VII (Fig. 4H), in ventral view, with posterior margin slightly emarginate. Pygofer (Fig. 4I), in lateral view, with posterior margin narrowly rounded; macrosetae distributed mostly on posterior half. Valvula I, in lateral view, with ventral interlocking device located on basal half of blade. Valvula II, in lateral view, with about 60 non-contiguous teeth.

The name of the new species, falcifera, refers to the falciform aedeagus (Fig. 4E).

Laussat (French Guiana).

French Guiana • ♂ holotype: “French Guiana: Laussat \ P3 \ 05°28′31.6″N - 053°35′07.3″W \ 12.ix.2010 \ Lamarre G. leg”; “White sand forest \ Light trap” (DZRJ). Paratypes • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 10.v.2011 \ window trap \ SEAG col.” (DZRJ) • 2 ♀♀: same data as preceding except “17.iv.2011” (DZRJ) • 1 ♀: “23.vii.2011” (DZRJ).

As mentioned in the key, D. falciferasp. nov. (Fig. 1C) shares with D. rafaelisp. nov. (Fig. 1I) the presence of a distinct red spot at the second apical cell of the forewing. The former can be readily distinguished from the latter, as well as from the remaining known species of the genus, by paraphyses with the apical portion of the rami, in lateral view, directed dorsally (Fig. 4G) and pygofer well produced posteriorly and with the posterior margin narrowly rounded (Fig. 4B).

♂ paratype 8.4 mm; ♂ 7.8 mm. Head (Figs 1E, 5A): in dorsal view, strongly produced anteriorly; median length of crown approximately 9/10 of interocular width and 5/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown flat; antennal ledge, in dorsal view, slightly protuberant; in lateral view, with anterior margin convex. Thorax (Figs 1E, 5A) with pronotum, in dorsal view, with width slightly greater than transocular width of head; lateral margins convergent anteriorly. Forewing with base of fourth apical cell approximately aligned with base of third.

Head, pronotum, and forewing mostly orange; mesonotum dull white. Frons mostly orange; clypeus pale yellow. Remainder of face (gena and lorum) and lateral and ventral portions of thorax pale yellow; legs mostly pale yellow to orange.

Pygofer (Fig. 5B), in lateral view, with posterior margin obliquely truncate; macrosetae distributed mostly on posterior third but some located more anteriorly. Subgenital plate (Fig. 5C), in ventral view, with basal third broad and distal two-thirds strongly narrowed; with elongate uniseriate macrosetae on basal third, microsetae distributed mostly along outer lateral margin. Connective (Fig. 5D), in dorsal view, T-shaped; stalk carinate dorsally, subequal in length to one arm width. Style (Fig. 5D), in dorsal view, somewhat S-shaped, slender, extending posteriorly beyond apex of connective; narrowed apically, apex obtuse. Aedeagus (Fig. 5E) symmetrical; shaft short, its whole ventral margin produced into strong process directed anteroventrally, posterior margin of process dentate; gonoduct distinct, gonopore located apically. Paraphyses slightly asymmetrical; elongate, extending well beyond subgenital plate apex; stalk shorter than rami (Fig. 5F) and, in lateral view, broadened posteriorly (Fig. 5G); rami, in lateral view, long and slender, their apexes spiniform (Fig. 5G).

Brazil, Pará State • 1 ♂: “Belterra – PA [Pará State] \ Faz. [Fazenda] Treviso \ 01-10/XII/2018 \ Marcela Monné \ Pedro S. Dias” (MNRJ) • 1 ♂ paratype: “Sta. [Santa] Isabel do Pará \ PA, Brasil \ 30.III.1962 \ J. Bechyné col.” (DZUP) • 1 ♂: “Canindé \ Rio Gurupi, PA \ IV.1963, Malkin \ & Pinheiros col.” (MZSP).

Cavichioli and Chiamolera (1999) considered D. isabellina (Fig. 1E) similar to D. basseti (Fig. 1A) in the male terminalia, especially the aedeagus. These two species can be distinguished from each other by the shape of the apex of the paraphyses rami, which are bifurcated in D. basseti (Fig. 2F) and not bifurcated in D. isabellina (Fig. 5F). The dorsal region of the body (Fig. 1E) is somewhat more orange in D. isabellina than in other species of the genus.

♂♂ 9.2–9.6 mm (n = 3). Head (Figs 1F, 6A): in dorsal view, well produced anteriorly; median length of crown approximately 8/10 of interocular width and 5/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown slightly concave; antennal ledge, in dorsal view, not protuberant. Thorax (Figs 1F, 6A) with pronotum, in dorsal view, with width slightly greater than transocular width of head. Forewing with base of fourth apical cell approximately aligned with base of third.

Head, pronotum, and mesonotum pale yellow. Forewing translucent with transverse broad orange stripe across bases of apical cells.

Pygofer (Fig. 6B), in lateral view, with posterior margin rounded; macrosetae distributed mostly on posterior half but some located more anteriorly. Subgenital plate (Fig. 6C), in ventral view, with basal half broad and distal half very narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 6D), in dorsal view, T-shaped; stalk not carinate dorsally, subequal in length to one arm width. Style (Fig. 6D), in dorsal view, slender, elongate, extending posteriorly beyond apex of connective; narrowed apically, apex obtuse. Aedeagus symmetrical (Fig. 6E, F); shaft short; in lateral view, somewhat sinuous; with pair of ventral, preapical sclerotized dentiform processes; dorsal margin dentate; gonoduct distinct, its apical portion slightly curved dorsally, gonopore located apically. Membrane connecting aedeagus to paraphyses with posterior sclerotized rugose lobe located close to aedeagal processes. Paraphyses slightly asymmetrical; elongate, extending well beyond subgenital plate apex; stalk shorter than rami; in dorsal view (Fig. 6G), stalk slender, rami divergent apically; in lateral view (Fig. 6H), stalk slightly arched dorsally, each ramus with dorsal lobe at midlength and acute apex.

French Guiana • 1 ♂: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 18.iii.2012 \ light trap (GEML) \ SEAG col.” (DZRJ) • 1 ♂: same data as preceding except “30.viii.2011” and “light trap (PSA)” (DZRJ) • 1 ♂: “FRENCH GUIANA: Réserve \ Naturelle de la Trinité \ Zone Aya: 4°36′3″N - \ 53°24′43″W, alt. 140m \ 01.vi.2012 \ light trap (PSA) \ SEAG col.” (DZRJ). Guyana • 1 ♂: “British Guiana: \ Essequibo R., \ Moraballi Creek. \ 14.viii.1929. \ Oxf. [Oxford] Uni. [University] Expedn. [Expedition] \ B. M. 1929-485.” (DZUP).

According to Young (1977), the body of D. mendica (Fig. 1F) is slenderer and more delicate than that of D. pauperata (Fig. 1H). Dasmeusa mendica can be distinguished from D. pauperata, as well as from the remaining known species of the genus, by the short and somewhat sinuous aedeagus, bearing a pair of ventral, preapical sclerotized dentiform processes (Fig. 6E, F).

♂ holotype 8.0 mm. Male holotype. Head (Figs 1G, 7A): in dorsal view, strongly produced anteriorly; median length of crown approximately 9/10 of interocular width and 6/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles, each ocellus approximately equidistant between median line of crown and adjacent eye angle; surface of crown depressed anteriorly; antennal ledge, in dorsal view, slightly protuberant. Thorax (Figs 1G, 7A) with pronotum, in dorsal view, with width slightly greater than transocular width of head; lateral margins convergent anteriorly. Forewing with base of fourth apical cell approximately aligned with base of third.

Head, pronotum, mesonotum, and forewing pale yellow.

Pygofer (Fig. 7B), in lateral view, with posterior margin rounded; macrosetae distributed on posterior half but some located more anteriorly. Subgenital plate (Fig. 7C), in ventral view, with basal half broad and distal half very narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 7D), in dorsal view, T-shaped; stalk much shorter than one arm width. Style (Fig. 7D), in dorsal view, slender, elongate, extending posteriorly well beyond apex of connective; slightly narrowed apically, apex obtuse. Aedeagus symmetrical (Fig. 7E); shaft short; ventral margin of shaft with preapical portion produced into robust process directed ventrally, posterior margin of process smooth; gonoduct distinct, gonopore located apically. Paraphyses symmetrical; elongate, extending well beyond subgenital plate apex; in dorsal view (Fig. 7F), stalk subequal in length to rami; rami slightly curved and crossing each other apically; in lateral view (Fig. 7G), stalk approximately rectilinear and with pair of strong dorsoapical processes, rami directed dorsally, narrowed apically.

Female unknown.

The name of the new species, oriximina, refers to the type locality (Oriximiná) in Pará State (Northern Brazil). It is a noun in apposition.

Brazil (Pará State).

Brazil, Pará State • ♂ holotype: “BR [Brazil]/ PA [Pará State] – Oriximiná \ Porto Trombetas \ 6-14.viii.2018 \ M.L. Soares & Y. \ Anthoinine \ Malaise [trap]” (DZRJ).

Dasmeusa oriximinasp. nov. (Fig. 1G) is similar to D. dinizisp. nov. (Fig. 1B) in the male terminalia, especially the aedeagus. The former species can be easily distinguished from the latter and other Dasmeusa species by the conspicuous dorsal processes of the paraphyses stalk (Fig. 7G).

♂♂ 9.5–10.8 mm (n = 5); ♀♀ 9.2–10.3 mm (n = 5). Head (Figs 1H, 8A): in dorsal view, well produced anteriorly; median length of crown approximately 8/10 of interocular width and 5/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown slightly concave; antennal ledge, in dorsal view, slightly protuberant; in lateral view, with anterior margin convex. Thorax (Figs 1H, 8A) with pronotum, in dorsal view, with width greater than transocular width of head. Forewing (Fig. 8B) with base of fourth apical cell approximately aligned with base of third; forewing of female at rest exceeding apex of ovipositor.

Head, pronotum, and mesonotum mostly brownish-yellow. Forewing yellow, preapical area with irregular orange transverse band. Face, lateral and ventral portions of thorax, and legs pale yellow.

Pygofer (Fig. 8C), in lateral view, with posterior margin broadly rounded; macrosetae distributed on posterior half but some located more anteriorly. Subgenital plate (Fig. 8D), in ventral view, with basal third broad and distal two-thirds strongly narrowed; with elongate uniseriate macrosetae on basal third, microsetae distributed mostly along outer lateral margin. Connective (Fig. 8E), in dorsal view, T-shaped; stalk not carinate dorsally, shorter than one arm width. Style (Fig. 8E), in dorsal view, somewhat S-shaped, slender, extending posteriorly beyond apex of connective; obtuse apically. Aedeagus symmetrical (Fig. 8F); shaft, in lateral view, with large ventral lobe and dorsoapical digitiform projection; without processes; gonoduct distinct, gonopore located apically. Paraphyses symmetrical; extending approximately as far posteriorly as aedeagal apex; stalk longer than rami; in dorsal view (Fig. 8G), stalk slender and rami fused at base, but strongly divergent at apical half, each ramus irregularly serrate and with small dentiform projection at basal portion (Fig. 8H); in lateral view (Fig. 8I), stalk sinuous, fused bases of rami robust and apices of rami directed dorsally.

Sternite VII (Fig. 9A), in ventral view, triangular, posterior margin rounded. Pygofer (Fig. 9B), in lateral view, with posterior margin narrowly rounded; macrosetae distributed mostly on posterior portion and extending anteriorly along ventral margin. “Internal” sternite VIII, in dorsal view, without sclerotized areas. Valvula I (Fig. 9C–E), in lateral view, with ventral interlocking device elongate, located on basal half of blade. Valvula II (Fig. 9F–I), in lateral view, with about 50 non-contiguous teeth.

Brazil, Amazonas State • 1 ♂: “BRASIL: AM [Amazonas State], 80km N [north of] \ Manaus, Reserva do \ PDBFF [Projeto Dinâmica Biológica de Fragmentos Florestais], Km 41 \ 02°24′S, 59°43′W \ 21-22.vii.2004” (DZRJ) • 1 ♂ and 2 ♀♀: same data as preceding except “22.xii-07.i.2005” (DZRJ) • 1 ♂ and 1 ♀: “16-17.ii.2005” (DZRJ) • 2 ♂♂: “05-06.viii.2004” (DZRJ) • 2 ♂♂: “24-25.xi.2004” (DZRJ) • 3 ♂♂ and 3 ♀♀: “08-09.xii.2004” (MNRJ) • 1 ♂: “18-19.viii.2004” (DZRJ) • 1 ♂ and 1 ♀: “15-16.ix.2004” (DZRJ) • 3 ♂♂ and 2 ♀♀: “19-21.i.2005” (MNRJ) • 2 ♂♂: “10-12.xi.2004” (INPA) • 3 ♂♂ and 7 ♀♀: “02-04.iii.2005” (INPA) • 3 ♂♂ and 1 ♀: “27-28.x.2004” (INPA) • 2 ♂♂: “09-10.vi.2004” (INPA) • 1 ♂ and 5 ♀♀: “30.iii-01.iv.2005” (DZRJ) • 1 ♂ and 5 ♀♀: “16-18.iii.2005” (INPA) • 1 ♀: “26-27.v.2004” (INPA) • 1 ♀: “07-08.vii.2004” (DZRJ) • 5 ♀♀: “02-04.ii.2005” (INPA) • 1 ♀: “12-13.v.2004” (INPA) • 2 ♂♂: “BRASIL: Amazonas, Barcelos, Rio \ Aracá, Com. [Comunidade] Bacuquara, \ 00.15309N 063.17743W \ Sweep 12-14/VI/2010 \ Takiya & Cavichioli” (DZUP) • 1 ♂: “Reserva [Florestal Adolpho] Ducke \ Manaus, Amazonas \ Brasil 11-XI-1976”; “Collector \ N. D. Penny” (DZUP) • 1 ♂: same data as preceding except “4-X-1976” (INPA) • 1 ♂: “Brasil, Amazonas, S. [São] Gabriel da \ Cachoeira, Rio Uaupés, PEF [Pelotão Especial de Fronteira] \ Querari, 15-30.v.2017 \ 01°04′51.3″N-69°50′32.1″W \ M.L. Oliveira & T. Mahlmann, \ Malaise [trap]” (INPA) • 5 ♂♂: same data as preceding except “1-15.vi.2017” (INPA) • 2 ♂♂: “15-30.vii.2017” (INPA) • 2 ♂♂: “Brasil, Amazonas, Manaus, ZF2 \ KM-14, 02°35′21″S-60°06′55″W \ 03-17.viii.2016 \ Malaise grande no chão \ J.A. Rafael & F.F. Xavier” (INPA) • 1 ♂: same data as preceding except “16-31.x.2016” (INPA) • 1 ♂: “1-15.ix.2016” (INPA) • 1 ♂: “BR [Brazil], AM, ZF-2, \ Km-14, 2°35′21″S - \ 60°06′55″W 28.viii.2019, \ solo, J.A. Rafael, N. Pecly \ & A.L. Diniz” (MNRJ) • 1 ♂: “2871”; “Est. [Estrada] Am1. Km 134 \ Mn. [Manaus] Am. [Amazonas State] Br. [Brazil] \ 10/08/68 \ Col – E. V. Silva \ & A. Faustino” (INPA) • 1 ♂: “XI Km 31 \ Manaus \ 21-V-1976 Am \ A.P.A. Luna Dias” (INPA) • 1 ♂: “BRASIL, Amazonas, \ Manaus, AM 010, Km 50 \ Ramal Vó Leuda 14-16. \ VI.2013 Luz mista \ F. Xavier D. Mendes \ P. Grossi & P. Bartholomay” (DZUP). Pará State • 1 ♂: “Utinga \ 7-12-1961”; “Brasil, PA [Pará State] \ J. & B. Bechyné” (MPEG) • 1 ♂: same data as preceding except “25.4.1961” (MPEG) • 1 ♂: “Brasil, Pará, Óbidos, \ Sítio Curió \ 29/VIII – 08/IX/2001”; “014703S 550705W \ Arm. [Armadilha] Malaise”; “J. A. Rafael & \ J. F. Vidal” (DZUP) • 2 ♂♂: same data as preceding except “29/VIII/2001” (INPA) • 1 ♂: “29/VIII/2001” (DZUP) • 1 ♂ and 1 ♀: “Canindé \ Rio Gurupi, PA [Pará State] \ IV.1963, Malkin \ & Pinheiros col.” (MZSP) • 1 ♀: “Benfica \ Ananindeua, PA \ 7.XI.1962 \ J. Bechyné col.” (MZSP) • 1 ♂: “Brasil Pará \ Belém Faz. [Fazenda] Vermelha \ 05-II-1981”; “Eniel Cruz” (MPEG) • 1 ♂: “Brasil Pará \ Benevides Faz. \ Morelandia \ 10-VI- a \ 02-VII-1988”; “Brasil Pará \ F.F. Ramos”; “Armadilha \ Malaise” (MPEG). Roraima State • 1 ♂: “BRASIL, RR [Roraima State], Amajari,\ Tepequém, SESC, 3°44′ \ 45″N-61°43′40″W, 1- \ 15.viii.2016, R Boldrini \ & JA Rafael, Malaise \ pequena, Rede Bia” (DZRJ) • 3 ♂♂: “BRASIL – Roraima \ Rio Uraricoera \ Ilha de Maracá \ 02-13.v.1987”; “J. A. Rafael \ J. E. B. Brasil \ L. S. Aquino”; “Armadilha de Malaise” (DZUP) • 1 ♂ and 2 ♀♀: “Brasil, Roraima, ESEC [Estação Ecológica] \ Maracá, Trilha Principal \ 24.iii.2016 \ Malaise \ A.P.M. Santos col.” (INPA) • 5 ♂♂: “Brasil, Roraima, ESEC \ Maracá \ 1-15.iii.2016 \ Malaise \ R. Boldrini” (INPA) • 2 ♂♂: “Brasil, Roraima, Alto Alegre, \ ESEC Maracá 3°21′59″N - \ 61°26′04″W, 1-15.x.2916, R. \ Boldrini & J.A. Rafael, \ Malaise pequena, Rede BIA” (INPA). Sergipe State • 1 ♂ and 1 ♀: “BRASIL, SE [Sergipe State], São Cristóvão \ 10°57′S 37°09′W \ A. P. Marques-Costa et al. \ 29-31.i.2010 \ Mata Atlântica YPT” (DZRJ). Bahia State • 1 ♂ and 1 ♀: “Belmonte - \ Barrolândia – BA [Bahia State] \ 1-VIII-1978 \ J. L. Nessimian”; “Estação \ Experimental \ Gregório \ Bondar” (DZRJ) • 1 ♀: “CEPLAC - ITA - \ BUNA [Itabuna] - BA. \ 1-VIII-1978 \ J. L. Nessimian” (DZRJ). French Guiana • 1 ♀: “FRENCH GUIANA: Petite \ Montagne Tortue P14 \ 04°19′14.1″N – 052°14′27.5″W \ 24.xi.2010 \ Lamarre G Leg”; “Terra firme clay forest \ Vitre trap (V10)” (DZRJ) • 1 ♀: “FRENCH GUIANA: Laussat \ P4 \ 05°28′31.6″N 053°35′07.3″W \ 30.ix.2010 \ Lamarre G. Leg”; “Terra firme clay forest \ Vitre trap (V 3)” (DZRJ) • 1 ♀: “FRENCH GUIANA: \ Belvédère de Saül \ 05/II/2010 \ SEAG leg. \ Malaise (M2)” (DZRJ) • 1 ♀: “FRENCH GUIANA: Montagne \ des Chevaux \ 4°44’56″N - 52°26’28″W, alt. 75 m \ 21.viii.2011 \ window trap \ SEAG col.” (DZRJ) • 1 ♂: same data as preceding except “16.vii.2011” (DZRJ) • 1 ♂: “01.iv.2012” (DZRJ) • 1 ♂: “08.v.2011” (DZRJ) • 1 ♀: “02.viii.2011” (DZRJ). Guyana • 1 ♂: “#CICA001 \ Eperua rubiginosa [host-plant] \ Camoudi 3-7.1997”; “Hand collecting/beating \ Station 5473 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “6179” (DZUP) • 1 ♀: “#CICA 001 \ Eperua rubiginosa \ Camoudi 15/02/1997”; “Hand collecting/beating \ Station 5473\ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “3739” (DZUP) • 1 ♂: same data as preceding except “9-9-1997” and “6068” (DZUP) • 1 ♂: “#CICA0001 \ Catostemma flagrans [host-plant] \ Camoudi 1-12.1996”; “Hand collecting/beating \ Station 3557 \ Seed\Sapl\Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “1111” (DZUP) • 1 ♂: “#CICA 001 \ Catostemma fragrans \ Camoudi 18-06-1997”; “Hand collecting/beating \ Station 5425\ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “7937” (DZUP) • 1 ♀: “#CICA001 \ Pentaclethra macroloba [host-plant] \ Camoudi 9.9.1997”; “Hand collecting/beating \ Station 6082 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “6636” (DZUP) • 1 ♂: “#CICA 001 \ Pentaclethra macroloba \ Camoudi 25/7/1996”; “Hand collecting/beating \ Station \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “2309” (DZUP) • 1 ♀: “#CICA 001 \ Chlorocardium rodiei [host-plant] \ Camoudi 12-3-1997”; “Hand collecting/beating \ Station 1711 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “4364” (DZUP) • 1 ♀: same data as preceding except “6.2-1997” and “4392” (DZUP). Suriname • 2 ♂♂ and 1 ♀: “Anapaike (Rio Lawa) \ Marowijne distr. [district] \ SURINAME \ XI.[1]968 B. Malkin” (DZUP) • 2 ♀♀: same data as preceding (MZSP).

Dasmeusa pauperata can be readily distinguished from the remaining known species of the genus by the aedeagus with a large ventral lobe and a dorsoapical digitiform projection (Fig. 8F). The shape of paraphyses, with strongly divergent arms, is also unique (Fig. 8G–I).

As mentioned above, Dasmeusa flavescens Metcalf, 1955 was proposed as a new name for Tettigonia lurida Signoret, 1853, which was preoccupied by T. lurida Germar, 1821. Young’s (1977) confirmation of Metcalf’s (1955) generic assignment was based on a study of the female lectotype of T. lurida (Fig. 10A–F), which is deposited in the Naturhistorisches Museum Wien. Young (1977) also suggested that D. flavescens, which was originally described from Brazil (Young 1977; Zanol and de Menezes 1982; McKamey 2007) and subsequently recorded from Suriname (Wilson et al. 2009), could be a junior synonym of D. pauperata (Fabricius, 1803). We have been able to study photographs of the T. lurida lectotype (Fig. 10A–F) and a female specimen from Pará State (“Belém \ Pará - Brazil \ IX.1964 \ E. Dente” [MZSP]). In agreement with Young’s (1977) suggestion, it appears to us that D. flavescens is actually a junior synonym of D. pauperata.

Young (1977: 1105) treated Erythrogonia bicolor Metcalf, 1949 as incertae sedis because he did not find specimens that could be associated with this name. We have examined a photograph of the male holotype (body in dorsal view) of E. bicolor, from Guyana, which is deposited at the entomological collection of the North Carolina State University, Raleigh (Fig. 11A). The external form and coloration, as well as the illustrations of the male terminalia provided by Metcalf (1949), suggest that this species is also a junior synonym of D. pauperata.

♂ holotype 8.0 mm; ♂ paratypes 7.6–8.0 mm (n = 2). Male holotype. Head (Figs 1I, 12A): in dorsal view, well produced anteriorly; median length of crown approximately 8/10 of interocular width and 5/10 of transocular width; anterior margin rounded; ocelli large, located approximately on imaginary line between anterior eye angles; surface of crown convex; antennal ledge, in dorsal view, not protuberant. Thorax (Figs 1I, 12A) with pronotum, in dorsal view, with width slightly greater than transocular width of head; lateral margins slightly convergent anteriorly. Forewing with base of fourth apical cell approximately aligned with base of third.

Head, pronotum, mesonotum, and forewing pale yellow; second apical cell of forewing with distinct red spot.

Pygofer (Fig. 12B), in lateral view, with posterior margin broadly rounded; macrosetae distributed mostly on posterior half but some located more anteriorly. Subgenital plate (Fig. 12C), in ventral view, with basal half broad and distal half narrow; with elongate uniseriate macrosetae on basal half, microsetae distributed along outer lateral margin. Connective (Fig. 12E), in dorsal view, V-shaped; stalk carinate dorsally, much longer than one arm width. Style (Fig. 12D), in dorsal view, slender, elongate, not extending posteriorly beyond apex of connective; narrowed apically, apex obtuse. Aedeagus (Fig. 12F), in lateral view, falciform, with apical spiniform process directed posteroventrally; gonoduct distinct, gonopore located apically. Paraphyses slightly asymmetrical; elongate, extending posteriorly beyond subgenital plate apex; stalk shorter than rami; in dorsal view (Fig. 12G), rami slender, slightly divergent posteriorly; in lateral view (Fig. 12H), rami narrowing gradually towards apex.

The name of the new species, rafaeli, is given in honor of Dr. José Albertino Rafael (Instituto Nacional de Pesquisas da Amazônia, Manaus) in recognition of his outstanding contribution to the knowledge of the Brazilian entomofauna.

Brazil (Amazonas State).

Brazil, Amazonas State • ♂ holotype: “BRASIL, AM [Amazonas State], Manaus, \ R. [Reserva] F. [Florestal] Ducke, AM-010 km 26 \ 02°25′49.5″S, 59°58′31.8″W \ Julho/Agosto 1979 \ Fumigação – Dossel \ T. E. Erwin”; “Brazil Canopy Fogging \ Project – July/August \ Dry Samples \ Trans. 10 (1 of 2)” (INPA). Paratypes • 1 ♂: “BR [Brazil], A.M., Manaus, ZF-2 \ Km-14, 2°35′21″S - \ 60°06′55″W 18.i- \ 01.ii.2019, YPT, 16mt. alt. \ J.A. Rafael - RedeBia” (DZRJ) • 1 ♂: “BRAZIL: AMAZONAS \ 18.1 Km e [east of] Campinas \ field sta. [station] Km 60 \ n Manaus 22Feb1979 \ 02°30′S 060°15′W”; “Montgomery, Erwin, \ Schimmel, Krischik, \ Date, Bacon colls.”; “Terra firme forest \ canopy fogged with \ Pyrethrum \ Sample #9” (INPA).

Brazil, Amazonas State • 1 ♂: “Brasil AM [Amazonas State] CEPLAC \ Manaus – Rod. [Rodovia] AM010 \ Km 30: 5.X.1977 \ Col. I.S. Gorayeb” (MPEG) • 1 ♂: “BRASIL: AMAZONAS \ 18.1 km e [east of] Campinas \ field sta. [station] Km 60 \ n Manaus 22Feb1979 \ 02°30′S 060°15′W”; “Terra firme forest \ canopy fogged with \ Pyrethrum \ Sample #24”; “Montgomery, Erwin, \ Schimel, Krischik, \ Date, Bacon colls.” (INPA). Guyana • 1 ♂: “#CICA 075 \ Catostemma fragrans [host-plant] \ Camoudi 24-10-1997”; “Hand collecting/beating \ Station 2809-1 \ Seed/Sapl/Tree”; “Mabura Hill \ GUYANA \ Y. Basset, Coll.”; “9086” (DZUP) • 1 ♀: same data as preceding except “25-10-1997”; “Station 3098-2”; “6926” (DZUP).

The color pattern of D. rafaelisp. nov. (Fig. 1I) is similar to that of D. falciferasp. nov. (Fig. 1C) because both have a distinct small red spot at the second apical cell of the forewing. The aedeagus of D. falcifera bears a conspicuous dentiform process at the basal half of the ventral margin (Fig. 4E), a feature that is not present in D. rafaeli (Fig. 12F).