Wyeomyia (Hystatomyia) intonca Dyar & Knab
publication ID |
https://doi.org/ 10.5281/zenodo.157376 |
publication LSID |
lsid:zoobank.org:pub:BBBE7852-70FA-40C8-9CCA-CB0B57E9EECF |
DOI |
https://doi.org/10.5281/zenodo.5628286 |
persistent identifier |
https://treatment.plazi.org/id/03FF87AF-3C14-FFD7-FEF8-FEF6FB80FE0B |
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Plazi |
scientific name |
Wyeomyia (Hystatomyia) intonca Dyar & Knab |
status |
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Wyeomyia (Hystatomyia) intonca Dyar & Knab View in CoL
( Figs. 3–6 View FIGURE 3 View FIGURE 4 View FIGURE 5 View FIGURE 6 )
Wyeomyia intonca Dyar & Knab, 1910: 173 View in CoL . Holotype ɗ, Empire, Canal Zone, Panama (USNM); examined. Synonymy with Wyeomyia (Dendromyia) circumcincta Dyar & Knab View in CoL by Lane, 1945: 146. Resurrected from synonymy and placed in subgenus Hystatomyia by Judd, 1998: 579.
Hystatomyia intonca: Dyar, 1919: 141 View in CoL , Pl. V (Fig. ɗ G).
Wyeomyia (Hystatomyia) intonca: Dyar, 1923: 170 View in CoL ( Panama: list); Dyar & Shannon, 1924: 91 ( Panama; list); Bonne & BonneWepster, 1925: 59,76 (Canal Zone; A key).
Prosopolepis (Hystatomyia) intonca: Dyar & Shannon, 1924: 482 (list); Dyar, 1925: 120, 124 ( Panama; collection records; L bionomics; ɗ G key).
Dendromyia intonca: Dyar, 1926: 43 , 44 (L description, bionomics); del Ponte, 1939: 540 (A).
Dendromyia (Hystatomyia) intonca: Dyar, 1928: 84 , Pl. XVIII (Fig. ɗ G, L; Ψ, ɗ, L; L bionomics).
Wyeomyia (Dendromyia) intonca: Edwards, 1932: 88 View in CoL ( Panama; list); Lane & Cerqueira, 1942: 606 (tentative synonym of circumcincta Dyar & Knab View in CoL ); Lane, 1945: 146 (synonym of circumcincta Dyar & Knab View in CoL ); Lane, 1953: 975 (synonym of circumcincta Dyar & Knab View in CoL ). Knight & Stone, 1977: 328 (synonym of circumcincta Dyar & Knab View in CoL ; info. on type).
Wyeomyia (Hystatomyia) View in CoL sp. D =? intonca: Heinemann & Belkin, 1978: 124 View in CoL , 160, 166. 194 ( Panama; collection records; L bionomics).
Life stages as described for Wy. chocoensis View in CoL with following exceptions:
MALE. Head: Frons with prominent puncture slightly below postfrontal suture. Ventral surface of proboscis with bright white scales from base to about 0.6 length where white scaling expands slightly (preapical patch) to ventrolateral margin; white scaling ends at about 0.75, replaced by dark scales to distal end. In many specimens, white scales are absent or very reduced slightly basad of preapical patch of white scales. Proboscis (P) (1.37–1.58 mm, mean 1.50 mm, n 5) longer than antennae (flagellum [F] 1.13–1.35 mm, mean 1.27, n 5), mean P:F, 1.18 (n 5), but shorter than forefemur, mean P:FeI 0.79 (n 5). Pedicel with 4–8 small setae dorsomesad. Flagellomere 1 with a primarily dorsomesad cluster of 5–10 scales; among 5 specimens (10 antennae) flagellomere 5 (Flm5) quite uniform in length (0.08 mm), flagellomeres 12 and 13 more variable (Flm12 0.10–0.14 mm, mean, 0.12; Flm13 0.16–0.20 mm, mean 0.19); mean Flm13:Flm5 2.29. Thorax: Integument brown. Supraalar and antealar areas have combined sum of 22–33 (mean 27, n 5) dark brown setae. Mesopostnotum brown with medial cluster of 6–9 (mode 8) pale, occasionally dark, setae. Prealar area with 3–5 yellow setae. Legs: Forefemur slightly longer than foretibia (mean FeI:TiI 1.04, n 5); forefemur somewhat shorter than midfemur (mean Fe I:FeII 0.89, n 5) but longer than hindfemur (mean FeI:FeIII 1.25, n 5); forefemur longer than proboscis (mean FeI:P 1.26, n 5); ventral surface of forefemur with white scales over basal 0.2, white scaling tapers to rather narrow line at about 0.4 and continues as narrow line along posteroventral surface to apex; posteroventral surface of foretarsomere 1 (TaI1) with white scales confined primarily to basal 0.5 and with darker scales with metallic reflection distally, in some specimens white scales extend as narrow line to distal end. Midfemur distinctly longer than midtibia (mean FeII:TiII 1.51, n 5); posteroventral surface of midtibia and basal 0.3–0.6 of midtarsomere 1 (TaII1) with bright white scales; midtarsomere 2 (TaII2) primarily with bright white scales, extent of basal dark scaling quite variable but more extensive on posteroventral surface (0.4–0.6 length of TaII2) than on anteroventral surface (0.2–0.3 length of TaII2), dorsal surface often with white scales over entire length, but may be diminished or even replaced by dark scales over basal 0.2. Ungues of midtarsomere 5 dissimilar; larger unguis stout, dark, curved sharply to about 90° angle, tip blunt with apical spur. Hindfemur slightly longer than hindtibia (mean Fe III:TiIII 1.04, n 5), hindtarsomere 1 slightly longer than hindfemur (mean TaIII1:FeIII 1.08, n 5), ventral surface of TaIII1 often with narrow line of white scales to ~0.75 length or with scattered white scales to near distal end. Ungues of hindtarsomere 5 slender, unequal; longer unguis 0.08 mm, about 2x length of shorter, with moderate to slight curvature; shorter unguis often strongly curved near base. Wing: 1.97–2.25 mm (mean 2.13 mm, n 5). Abdomen: Lateral margins of abdomen with creamy white scales, which form an essentially straight line along abdomen; sterna covered with creamy white scales. Distal margin of sterna II–V with about 7–12 small pale setae, more numerous and longer pale setae along distal margin of sterna VI (~19) and VII (~24). Genitalia ( Fig. 3 View FIGURE 3 CG): Tergum VIII (ventral in position) narrow, 3.4–4.7x as wide as long; covered with small spicules, which become minute and very numerous basally although basal 0.3–0.5 glabrous; distal margin straight, 3 irregular rows of long dark setae (range 38–41, mean 40, n 6) along and near distal margin, longest setae about 2.1–2.5 times length of tergum VIII along median plane. Sternum VIII (dorsal in position) with distal margin somewhat convex; setae (range 23–27, mean 25, n 6) dark, arranged primarily as single row along distal margin; a few scales along lateral margins pale, rest dark. Tergum IX bearing 3, rarely 2, stout but relatively short setae on either side of narrow median bridge, apices of setae bent slightly laterad. Sternum IX narrow but expanded medially, becoming bellshaped between base of gonocoxites; appears to be fused basally to gonocoxites; with rather broad Ushaped mesal membranous area; quite densely spiculate. Gonocoxite elongate, expanded basally; sternal basal surface spiculate with rather sparse covering of scales, an irregular row of setae just proximal to basal mesal setal clusters of tergum. Distal 0.5 of gonocoxite slender, distinctly bowed; mesal surface with slender setae distally that merge with dense subapical/ apical cluster of dark setae (0.2–0.3 length of gonocoxite); setae on or near mesal margin curved distally toward median plane of genitalia. Tergal surface of gonocoxite with 4 prominent clusters of setae (3 occur close together in a basal mesal position): (1) basalmost cluster comprised of 10–13 (mean 11) unmodified, moderately developed pale setae; (2) adjacent to this cluster (slightly mesad and distal to it) is a group of 11–15 (mean 14) stout, rather long setae (~ 0.4 length of gonocoxite) with golden reflection, which terminate in curved spathelike apex (a few smaller unmodified setae occur along edge of this cluster); (3) ventral (prerotation sense) and often slightly distal to these setae is a third group of 9 (rarely 10) somewhat longer (~ 0.5 length of gonocoxite), lanceolateshaped setae with golden to copper reflection, these setae become slightly broader subapically before bending sharply and narrowing to a fine tip; (4) fourth prominent cluster of setae laterad to three basal mesal clusters, usually consists of 28–41 (mean, 34) unmodified pale setae, longest often extending slightly beyond tip of gonocoxite. Gonostylus ( Fig. 3 View FIGURE 3 D) arises basally on gonocoxite near mesal margin of lateral setal cluster; the glabrous and relatively transparent gonostylus extends mesally, then curves distally and becomes broader; expanded apical area about 3x width of basal portion (stem). Aedeagus slightly longer than wide; submedian tergal arms bend toward each other resembling an upsidedown V, in some individuals the arms appear to be joined medially but in others they appear to remain slightly separated. Proctiger (in lateral view) with broad basal sclerotization of tergum X, paraproct with rounded apex and bearing 4–7 cercal setae.
FEMALE. Like male except for sexual characters as follows. Head: Ventral surface of proboscis often entirely dark scaled with exception of small cluster of white scales (preapical patch) from 0.6–0.7 length of proboscis; less frequently a narrow line of white scales extends from base of proboscis to preapical patch. Thorax: Integument light brown to brown. Legs: Resembling male but with several differences. Dorsal surface of midtarsomere 1 (TaII1) with dark scales, white scales limited to basal 0.3 of posteroventral surface, most numerous on basal 0.1; midtarsomeres 2–5 (TaII2–5) ( Fig. 6 View FIGURE 6 A) with dark scales with metallic reflection, a few pale and white scales may be present near basal and/or distal end of TaII2–4; TaII5 with variable amount of pale scaling. Genitalia ( Fig. 5 View FIGURE 5 AD): Tergum VIII wider than long (width 0.43–0.48 mm, length along median plane 0.17–0.19 mm, n 2); covered with minute spicules and spatulate scales; distal margin slightly concave; setae confined to distal 0.5, most numerous along and near distal margin, absent from lateral margins, in total about 46–54 setae. Distal margin of sternum VIII with numerous strong, straight to slightly curved setae, which expand basally to form a mesal Vshaped cluster; in total about 55–69 setae. Insula wider than long, covered with moderately long spicules; apex broadly rounded to rather truncate, irregular anterolateral row of 5 or 6 small setae on either side of midline; mesal semicircular depression or cavity opening onto basal margin, prominent spicules along lower edges of opening. Dorsal postgenital lobe length 0.11 mm, dorsal postgenital lobe index 1.83–1.87 (see Reinert, 1974). Cercus rather flat; covered with minute spicules; apex rather truncate; dorsal surface with 12–16 setae, longest 0.6– 0.7 length of dorsal postgenital lobe.
PUPA ( Fig. 3 View FIGURE 3 A,B). Position and character of setae as figured; numbers of branches presented in Table 3. Cephalothorax: Tan with very pale to clear patches, especially along dorsal margin of scutal protrusion at base of trumpet. Seta 4CT usually with 3 or 4 branches. Metathoracic wing tan with pale markings comprised of submedial pale spot and a slightly pale spot on each lateral margin. Trumpet: Length 0.84–1.26 mm (mean 1.08 mm, n 8); tan, darkest basally, distal end not quite as dark and slightly flared, medial portion similar in color to distal end or slightly paler. Abdomen: Abdominal tergum I rather uniformly tan although seta 6,7I and occasionally 4,5I within a pale spot. Seta 1I well developed, most often with 18 or 19 branches. Seta 3I moderately developed, usually double; seta 3IV–VI about onethird the length of 3III, 3IV with 3 or 4 branches, 3V usually 4branched, 3VI 2–4branched. Seta 5I single, infrequently double; seta 5II,III relatively small (approx. 0.2 mm), usually 4branched; 5IV–VI single, very long (approx. 1.1–1.2 mm). Puncture near seta 4III–V, usually located distolaterad of seta 4III,IV and basal mesal to seta 4V. Paddle: Pale tan, somewhat darker along midrib. Male genital lobe: Large (length [l] 0.57–0.62 mm, mean 0.60 mm, n 8; width [w] 0.50–0.54 mm, mean 0.52 mm, n 8; mean l:w 1.14, range 1.11–1.16) with ellipticalshaped apex; distinctly broader than combined width of paddles.
Cephalothorax Abdominal segments
Seta no. CT I II III IV V VI VII VIII
0 – – 1 1 1 1 1 1 1 1 Range followed in parenthesis by mode; based on 8 specimens (16 setae). 2 One exception from number in parenthesis.
3 Very small, occasionally with seta with 1 or 2 branches.
Head Thorax Abdominal segments 1 Range followed in parenthesis by mode; based on 8 specimens (16 setae). 2 One exception from number in parenthesis.
FOURTHINSTAR LARVA ( Fig. 4 View FIGURE 4 ). Position and character of setae as figured; numbers of branches presented in Table 4 View TABLE 4 . Head: Dorsomentum with 1 large central tooth and 9–11 pairs of smaller lateral teeth. Maxilla: Maxillary brush quite long, maxillary brush spicules similar in length to seta 4Mx (0.23 mm). Seta 1Mx short, stout (0.015 mm); seta 2Mx very slender, approx. 0.025 mm in length, basal to 1Mx. Mandible: Mandibular rake comprised of approximately 8 stout spicules, each about 0.12 mm in length. Antenna: Short (mean 0.29 mm, n 10), slender; seta 1A 2branched (rarely single), borne dorsally about 0.68 (mean of 10) length and usually not quite reaching tip of antenna. Thorax: Seta 14P single, sometimes forked or 2branched. Seta 2M less than 0.5 length of 3M, base of 2M slightly narrower than base of 3M; 7M about 0.25–0.33 length of 5M; 9,10M long, similar in length. Abdomen: Seta 2I laterad of 1I, stout, often 2branched; 2II usually single, basal to 1II; 2III–VII distinctly mesad of 1III–VII. Seta 3I more than twice length of 2,4I; 6VII 4–6branched, rather short; 10VI usually 4branched. Seta 11I prominent, stellate, branches similar in length to those of 13I. Segment VIII: Comb scales in 4 or 5 irregular rows (mean number of scales 69, range 58–76, n 9). Seta 2VIII single, rather long, about 0.5 length of siphon. Siphon: Long, slender (mean length 1.17 mm, range 1.04–1.28 mm, n 12) usually somewhat curved distally, wider at base, lightly pigmented with subapical region of darker pigmentation and basal edge quite dark, surface smooth; siphon index 7.8–8.9 (mean 8.2, n 11). Pecten comprised of 5–8 (mode 6, n 12) spinelike spicules, somewhat fringed apically; basal spicule close to seta 1S, often slightly distal to it. Seta 1S usually with 3 or 4 branches; located basally at about 0.13 (mean of 12) of siphon’s length. Ventral accessory setae (1aS) unbranched, arranged in 2 rows; number of setae in 2 rows combined 12–16 (mean 14, n 12); length of distalmost seta usually slightly shorter than distance of seta to distal end of siphon. Dorsal accessory setae (2aS) unbranched, infrequently a distal seta is forked; arranged in 2 rows; number of setae in 2 rows combined 11–19 (mean 17, n 14); basalmost seta approximately same length as third and fourth setae from base; distal seta not extending to tip of siphon. Segment X: Saddle tan, similar in color to darkened subapical area of siphon; extending near to ventral surface, mean length of 0.22 mm (n 12) measured dorsally. Setae 1– 3 X well developed; setae 1,3 X 2 branched, all long; 2X 3branched, smallest (upper) branch about 0.4–0.8 length of middle branch, which is quite variable, and about 0.25–0.33 length of lower branch; seta 4X 7–10branched (mode 8,9, n 23), about 0.30 mm in length.
BIONOMICS. Wyeomyia intonca originally was described from a male, which had been collected as a larva or pupa from a bromeliad on a fallen tree at the edge of Comacho river, Canal Zone, Panama (Dyar & Knab, 1909). In 1925 Dyar indicated larvae of Wy. intonca occur in Tillandsia , and in 1926 published a brief description of the larval stage from specimens found in “wild pineapple, Ananas magdalenae (André) Standl. ” These plants were found in “jungle, some three miles back of Fort Randolph on the Atlantic side of the Isthmus.” Heinemann & Belkin (1977a, b, 1978) reported collections of Wy.? intonca (3 different forms designated D, G and H) from 15 bromeliad samples ( Panama, 5; Costa Rica, 9; and Nicaragua, 1), which were primarily from forested areas at elevations of 100 m and 500– 700 m. However, only Wy. ( Hystatomyia ) sp. D appears to correspond with Wy. intonca , and it was encountered only in Panama. Our collections, upon which the redescription is largely based, were from the northern Pacific Coast of Colombia, specifically Ensenada de Utria and southward to Jurubida. In this region, Wy. intonca was closely associated with coastal mangroves, which tended to be quite variable with respect to dominant tree species. Piñuelo mangrove dominated by Pelliciera rhizophorae Tr. & Pl. (Pellicieraceae) and with numerous tank bromeliads (dominants include: Werauhia ringens [Griseb.] J.R. Grant, W. sanguinolenta [Linden ex Cogniaux & Marchal] J.R. Grant, and W. gladioliflora [H. Wendland] J.R. Grant) appeared to be a particularly suitable habitat for Wy. intonca . This mosquito also was abundant in red mangrove dominated by Rhizophora harrisonii Leechm. and R. mangle L. ( Rhizophoraceae ); dominant tank bromeliads include W. sanguinolenta , W. gladioliflora , W. kupperiana (Suess.) J.R. Grant , and Aechmea pubescens Baker. Within these mangroves, larvae of Wy. intonca were found in tank bromeliads located from 0.6 to 2.5 m above ground and were found primarily in larger plants, i.e., those with 0.5 to 1+ liters of water. Wyeomyia intonca was not encountered in bromeliads from forested areas adjacent to these mangroves, even though sampling was quite extensive.
DISTRIBUTION. Collection records from Panama suggest the distribution of Wy. intonca extends from the Canal Zone to Colombia. At present, the known distribution of this mosquito in Colombia is limited to our collections from the northern Pacific Coast of the Department of Chocó (Ensenada de Utria and southward to Jurubida).
MATERIAL EXAMINED.
Sixtyseven specimens (22ɗ, 4Ψ, 10ɗG, 3ΨG, 4Le, 15Pe, 9L), including 4 complete and 11 partial individual rearings. Holotype, ɗ, genitalia on microscope slide, PANAMA: DK, 509, Type No. 12744 U.S. N.M. (red tag). Nontypes, PANAMA: Canal Zone, Gatun, Jan. 1928 (1ɗ 1ɗG 1LePe ɗ 11146m with dissected genitalia), (C.H. Bath Coll.), (blue tag). COLOMBIA: Chocó, Ensenada de Utria (6°03.1'N 77°21.5'W), 18II1999 (3ɗ 1Ψ 1ΨG 2LePeɗ 1Peɗ 1L – CO11433, 4, 6, 101 with dissected genitalia, 102), 0–10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant , (Wolff & Porter ); same locality, 18II1999 (1L – CO114419), 0–10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant , (Wolff & Porter ); same locality, 18II1999 (1L – CO11458), 0–10 m, hbt: Guzmania scherzeriana Mez , (Wolff & Porter ); same locality, 18II1999 (1ɗ 1ɗG 1Peɗ 1L – CO11478, 103 adult on microscope slide with dissected genitalia), 0–10 m, hbt: Guzmania scherzeriana Mez , (Wolff & Porter ); same locality, 18II1999 (1ɗ 1Peɗ 1L – CO11488, 104), 0–10 m, hbt: Werauhia ringens (Griseb.) J.R. Grant , (Wolff & Porte r); same locality, 18II1999 (3ɗ 1ɗG 1Ψ 1LePeɗ 1Peɗ – CO114925, 112, 114 with dissected genitalia, 121), 0–10 m, hbt: Werauhia ringens (Griseb.) J.R. Grant , (Wolff & Porter ); same locality, 24VI1999 (2ɗ 1Peɗ – CO111065, 101), 0–10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant , (Wolff & Porter ); same locality, 27VI1999 (1ɗ 1Peɗ 2L – CO1117114, 118), 0–10 m, hbt: Werauhia ringens (Griseb.) J.R. Grant , (Wolff & Porter ); same locality, 27VI1999 (1ɗ 1ɗG 2L – CO111724, 21 adult on microscope slide with dissected genitalia), 0–10 m, hbt: Werauhia ringens (Griseb.) J.R. Grant , (Wolff & Porter ); Chocó, Ensenada de Utria (6°01.3'N 77°21.0'W), 20II1999 (1ɗ – CO11754), 0–10, hbt: Werauhia gladioliflora (H. Wendland) J.R. Grant , (Wolff & Porter ); Chocó, Nuquí, Jurubida, Río Chori (5°50'N 77°17'W), 19II1999 (7ɗ 5ɗG 2Ψ 2ΨG 4Peɗ 1PeΨ – CO1170 104 adult on microscope slide with dissected genitalia, 119 adult on microscope slide with dissected genitalia, 103, 112 with dissected genitalia, 114 with dissected genitalia, 116 adult on microscope slide with dissected genitalia, 120 adult on microscope slide with dissected genitalia, 137, 144, 145, 148 with dissected genitalia), 0–10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant , (Wolff & Porter ).
Seta no. | C | P | M | T | I | II | III | IV | V | VI | VII | VIII X |
---|---|---|---|---|---|---|---|---|---|---|---|---|
0 | 1 | 12–17 (14) | – | – | – | 1 | 1 | 1 | 1 | 1 | 1 | 1 – |
1 | 1 | 9–14 (12) | 11–15 (15) | 8–14 (11) | 7–11 (9) | 6–10 (7,8) | 6–8 (6) | 5–7 (7) | 5–7 (7) | 5–8 (6) | 5–8 (6) | 12–17 2 (14) |
2 | – | 1 | 1 | 1,2(1)2 | 1–3(2) | 1,2(1) | 1 | 1 | 1 | 1 | 1 | 1 3 |
3 | 1 | 4–6 (5) | 1 | 2–4 (3) | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 5–9 2 (7) |
4 | 8–15 (12)1 | 2 | 2,3 (2) | 3,4 (3)2 | 2,3 (2) | 2,3 (2) | 1–3 (2) | 1–3 (2) | 3,4 (3)2 | 2 | 1 | 2–4 7–10 (3) (8,9) |
5 | 4–8 (7) | 1 | 1 | 12–17 (15) | 3–6 (4) | 4–6 (5) | 4–6 (5) | 4–6 (5) | 5,6 (5) | 5–7 (5,6) | 4–6 (5) | 5 – |
6 | 4–8 (6) | 2 | 1 | 1 | 5–7 (6) | 3,4 (3) | 2 | 2 | 2 | 2 | 4–6 (5) | – – |
7 | 7–13 (9) | 1 | 1 | 10–13 (11) | 3–5 (4) | 3 | 3 | 6–9 (7) | 6–9 (7) | 5–9 (6,7) | 1,2 (1)2 | – – |
8 | 4,5 (4) | 10–14 (11) | 5–7 (6) | 6–12 (7,9) | – | 2,3 (2) | 2–5 (4) | 1,2 (2) | 1–3 (2) | 5–8 (7) | 9–13 (11) | – – |
9 | 8–10 (9) | 1 | 1 | 6–8 (6) | 3–7 (5) | 4–7 (6,7) | 5–8 (6) | 5–8 (5) | 4–6 (5) | 4–6 (5) | 5–9 (6) | – – |
10 | 4–6 (4) | 1 | 1 | 1 | 1 | 1–3 (2) | 2,3 (3) | 2–4 (3) | 3–5 (4) | 3–6 (4) | 2,3 (2) | – – |
11 | 3,4 (4) | 6–9 (7,8) | 6–9 (6,7) | 4–7 (5) | 5–9 (7) | 3,4 (3) | 2,3 (3) | 2–5 (3) | 2–5 (3) | 3–5 (3,5) | 4–7 (4) | – – |
12 | 3–5 (4) | 1 | 1 | 1 | – | 2–4 (2) | 1 | 1 | 1 | 1,2 (1) | 3–6 (4) | – – |
13 | 3,4 (3) | – | 10–16 (14) | 8–12 (10) | 4–8 (5,6) | 6–8 (6) | 4–8 (6,7) | 6–9 (6) | 5–8 (7) | 5–7 (7) | 6–8 (7) | – – |
14 | 1,2 (2)2 | 1,2 (2) | 6–9 (8) | – | – | – | – | – | – | – | – | 1 – |
15 | 2–4 (3) | – | – | – | – | – | – | – | – | – | – | – – |
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.
Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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Genus |
Wyeomyia (Hystatomyia) intonca Dyar & Knab
Porter, Charles H., Wolff, Marta I. & E 2004 |
Wyeomyia (Hystatomyia)
Heinemann 1978: 124 |
Wyeomyia (Dendromyia) intonca:
Knight 1977: 328 |
Lane 1953: 975 |
Lane 1945: 146 |
Lane 1942: 606 |
Edwards 1932: 88 |
Dendromyia (Hystatomyia) intonca:
Dyar 1928: 84 |
Dendromyia intonca:
Ponte 1939: 540 |
Dyar 1926: 43 |
Prosopolepis (Hystatomyia) intonca:
Dyar 1925: 120 |
Wyeomyia (Hystatomyia) intonca:
Bonne 1925: 59 |
Dyar 1923: 170 |
Hystatomyia intonca:
Dyar 1919: 141 |
Wyeomyia intonca
Judd 1998: 579 |
Lane 1945: 146 |
Dyar 1910: 173 |