Montina gladiator Mejía-Soto & Forero, 2022
publication ID |
https://doi.org/ 10.37520/aemnp.2022.019 |
DOI |
https://doi.org/10.5281/zenodo.10552727 |
persistent identifier |
https://treatment.plazi.org/id/039387AD-137B-FFB8-FC91-B6DA42DFD008 |
treatment provided by |
Felipe |
scientific name |
Montina gladiator Mejía-Soto & Forero |
status |
sp. nov. |
Montina gladiator Mejía-Soto & Forero , sp. nov.
( Figs 13 View Fig ; 14 View Fig ; 25A View Fig ; 27A View Fig ; 29A View Fig ; 41 View Fig )
Type locality. Colombia: Chocó: Riosucio, Sautatá.
Type material. HOLOTYPE: COLOMBIA: CHOCṒ: 1 ♂, Riosucio, Sautatá ; [07.4431°N, 77.1014°W]; Jul 1978; H. Echeverri leg., ICN 029956 View Materials / (red label) HOLOTYPE Montina gladiator A. Mejía-Soto & D. Forero , sp. nov. ( ICN) GoogleMaps . PARATYPES: COLOMBIA: CHOCṒ: 1 ♀, Riosucio, Tilupo ; [07.4383°N, 77.1151°W]; Abr 1978; H. Echeverri leg.; ICN 036201 ( ICN) GoogleMaps ; 2 ♀♀, same data; 12 Jun 1978; ICN 029954, ICN 029953 ( ICN); 1 ♀, same data; 27 Jul 1978; ICN 029955 ( ICN); 1 ♀, Quibdó, Yuto; [05.5340°N, 76.6308°W]; 90 m; 1 Nov 1983; F. Serna leg.; en maleza; MEFLG No.7279 ( MEFLG). SANTANDER: 1♂, Guapotá, Carare; [06.3335°N, 73.3360°W]; 800 m; 3 May 1939; L. Richter; CTNI: No. 2539 ( CTNI); 1 ♀, Landázuri; [06.2194°N, 73.8092°W]; 1000 m; 3 Ene 1938; L. Richter; CTNI: No. 2539 ( CTNI). TOLIMA: 1♀, Mariquita; [05.1995°N, 74.8868°W]; 29 Ago 1987; MPUJ _ENT0058602 ( MPUJ).
Diagnosis. Total length, females 23.5–24.0 mm (n = 3), males 16.3–19.0 mm (n = 2). General coloration red, with legs, scutellum, and abdomen black ( Figs 13B, D View Fig ); membrane translucent yellow; tubercle of the anterior pronotal lobe subconical with rounded apex, posterior pronotal lobe elevation of the carina truncated with its posterior margin slightly rounded ( Figs 13E–F View Fig ); connexivum dark brown to black with a red narrow band on its margin, sometimes a little diffuse ( Figs 13A–D View Fig ), segments 4–5 lobed, 6 straight, segments 2–4 with an acute posterior process on each segment, in males the processes are more conspicuous and also present in segment 5 ( Figs 13A, C View Fig ).
Description. Male. Total length 16.3–19.0 mm, head length, 3.6–3.8 mm, anterior pronotal length, 1.0– 1.1 mm, posterior pronotal lobe length 2.2–2.9 mm, abdomen width 4.9–7.6 mm (n = 2). COLORATION. Head red to light red; scape and pedicel dark brown, flagellomeres reddish; labium brown, first visible segment dark red. Thorax: Anterior and posterior pronotal lobes red; pro-, mesoand metasternum brown. Legs: Coxae reddish, remaining segments of legs from dark brown to black. Hemelytron: Corium red, anterior margin of corium (R+M) dark red; membrane translucent yellow. Abdomen: Sternites dark brown with darker bands on segments 2–6; connexival segments dark brown to black with a narrow red band on its margin; pygophore bright yellow. VESTITURE. Body moderately setose. Head covered mainly by medium sized and short sized setae, and few longer setae on the postocular area and clypeus. Thorax: Anterior pronotal lobe with glabrous areas; posterior lobe less setose than anterior lobe, posterior margin with long setae; fore leg ventrally covered by dense, medium sized setae. Abdomen: Sternites and ventral laterotergites covered by decumbent golden setae; ventrolateral area of abdominal sternites with erect black setae near the posterior margin. STRUCTURE. Head: Eyes globular, prominent in dorsal view, about half the width of postocular area, ovoid in lateral view with posterior margin nearly straight; first visible labial segment shorter than second. Thorax: Tubercles of anterolateral angles slightly prominent, apically acute; discal tubercles of anterior pronotal lobe subconical, apically rounded; elevation of the carina of the posterior pronotal lobe truncated, posterior margin slightly rounded; pronotal posterolateral process broadly triangular, apically rounded; scutellum short, apex slightly rounded but ends at a small tip. Membrane extends beyond the abdomen. Abdomen: Margin of connexival segments 2–3 straight, 3 with sharp posterior projection, 4–5 lobed each with subangular process posteriorly, more conspicuous on 4, 6–7 straight. Genitalia: Pygophore ovoid in lateral view, in dorsal view wider posteriorly ( Fig. 14A View Fig ); medial process (mpp) with parallel margins, cylindrical, in lateral view, straight, directed at about 45 degrees ( Figs 14A–C View Fig ); paramere slightly curved, body narrow on basal half, distal portion widened and rounded, apically with long setae ( Figs 14A, C View Fig ); articulatory apparatus (apt) with basal plate arms about as wide as basal plate bridge, lumen about as wide as one arm width ( Fig. 14F View Fig ); dorsal phallothecal sclerite (dps) narrowing apically, apex truncated and slightly emarginated, in lateral view dps concave; endosoma with distal ventral lobe (dvl) with numerous sclerotized microtrichia ( Fig. 14D View Fig ); distal dorsal lobe (ddl) oval; distal lateral lobes (dll) strongly sclerotized at margin; lateral lobes (ll) tear-shaped ( Fig. 14D View Fig ).
Female. Similar to male but larger, except in the following: total length 23.3–23.5 mm, head length 4.2–4.3 mm, anterior pronotal lobe length 1.2–1.4 mm, posterior pronotal lobe length 3.8–3.9 mm, abdomen width 7.7–10.0 mm (n = 3). COLORATION. Similar to the male, usually darker; pronotal lobes uniform in coloration. STRUCTURE. Thorax: Discal tubercles of anterior pronotal lobe larger, apex of equal width; elevation of carina of posterior pronotal lobe truncated ( Fig. 13F View Fig ). Abdomen: Connexival margin of segment 3 subtriangular, 5 less lobed than in male with smaller subangular process ( Fig. 13C View Fig ). Genitalia: Gonocoxa 8 subquadrangular, anterior margin (am) straight; gonoplac (gpl) apically slightly projected beyond joining area, obtuse, thick, glabrous; syntergite 9/10 with distal portion (dp) curved, in ventral view concave ( Fig. 25A View Fig ); bursa copulatrix trapezoidal, anterior margin straight; lateral protruding lobes (lbs) very wide, exceeding margin of anterior portion ( Fig. 27A View Fig ); U-shaped structure of dorsal area of bursa strongly sclerotized ( Fig. 29A View Fig ).
Variation. The examined specimens from Chocó and Tolima have a darker coloration than those from Santander, although they all share the same coloration pattern. No other variation was observed.
Differential diagnosis. Montina gladiator sp. nov. resembles M. calarca sp. nov., M. nigripes , and M. scutellaris because of the reddish coloration of the thorax and the margin of the connexivum, but easily distinguishable by the red coloration of the head ( Figs 13B, D, G View Fig ), which is either black or dark brown in the other species. Both M. gladiator sp. nov. and M. nigripes have the connexival margin of segment 6 nearly straight ( Figs 13A, C View Fig ; 35A View Fig ) in both sexes, in contrast to having it lobed in M. calarca sp. nov. and M. scutellaris ( Figs 5A, C View Fig ; 19A, C View Fig ), although in the latter it is more conspicuous in males.
Etymology. The name is taken from the Latin gladiator , referring to the gladiators of ancient Rome because of the red coloration of their cape and tunica, similar to the coloration of the new species. The name is treated as a noun in apposition.
Distribution. Only known from Chocó, Santander, and Tolima in Colombia, with records ranging between 90–1000 m. ( Fig. 41 View Fig ).
It is noteworthy that many of the known localities of M. gladiator sp. nov. are the same as those of M. scutellaris ( Figs 41 View Fig ; 42 View Fig ), although the new species was found restricted to lowland areas (below 1,000 m), whereas M. scutellaris can reach areas up to 1,600 m. Other species of Montina are apparently also sympatric, as in the case of M. confusa , M. distincta , and M. testacea ( Figs 40 View Fig ; 42 View Fig ). Given the paucity of specimens of M. gladiator sp. nov. found among the examined material, it is unknown if M. gladiator sp. nov. is locally rare or if it is occupying a different habitat from that of M. scutellaris , thus being harder to collect in the field. Future fieldwork is required to explore these ideas.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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