Myrmecotypus dacetonoides ( Mello-Leitão, 1948 ) Silva-Junior & Bonaldo, 2024
publication ID |
https://doi.org/ 10.11646/zootaxa.5555.4.1 |
publication LSID |
lsid:zoobank.org:pub:24FACE7D-F2B3-47CB-BF71-FF85CBECE77C |
persistent identifier |
https://treatment.plazi.org/id/03B787E5-CF0A-FFFB-0ED7-B3831E76F9A2 |
treatment provided by |
Plazi |
scientific name |
Myrmecotypus dacetonoides ( Mello-Leitão, 1948 ) |
status |
comb. nov. |
Myrmecotypus dacetonoides ( Mello-Leitão, 1948) comb. nov.
Figs 9A–G View FIGURE 9 , 10A View FIGURE 10 –IE, 11A–I, 12A–N
Apochinomma dacetonoides Mello-Leitão, 1948: 182 View in CoL , 23 (holotype, ♀, Forest near Camp I, Upper Curuyuni, BRITISH GUYANA: 13.IV.1933, leg. J.S. Carter, in Natural History Museum, London, NHM 1933.11.27.2, examined)
Myrmecotypus iguazu Rubio & Arbino, 2009: 66 View in CoL View Cited Treatment , 1–12 (holotype, ♂, ARGENTINA: Iguazu National Park , Misiones Province , in Museu Argentino de Ciências Naturales, Argentina, MACN-Ar 19708; examined by photos) syn. nov.
Note. Other than the fact that no consistent differences were recorded in the genitalic morphology among the examined specimens, the synonymy of Myrmecotypus iguazu View in CoL with M. dacetonoides View in CoL comb. nov. is justified by the following lines of evidence. The female holotype of Apochinomma dacetonoides View in CoL ( Fig. 9 View FIGURE 9 ), as in the female paratypes of M. iguazu View in CoL syn. nov. ( Fig. 11 View FIGURE 11 ), has two promarginal and two retromarginal teeth ( Rubio & Arbino, 2009, fig. 10) and a V-shaped epigynal transverse ridge with sclerotized corners ( Fig. 9B View FIGURE 9 ; Rubio & Arbino 2009: figs 8, 9). In the original description of M. dacetonoides View in CoL comb. nov., Mello-Leitão (1948) describes the tibia I ventral spination as 3- 3 (2-2-2). However, this is a lapsus, as that specimen presents a 1p-2-2 (3-2) pattern ( Fig. 9G View FIGURE 9 ). The tibia I spination of M. iguazu View in CoL is reported to be 3- 3 in both sexes ( Rubio & Arbino 2009). Most males and females here attributed to M. dacetonoides View in CoL comb. nov. have a tibia I ventral spination 3-2 ( Figs 12D–E, I–J View FIGURE 12 ), with the exception of a female specimen (MZUSP-7779, from Caraguatatuba, state of São Paulo, southeastern Brazil) that presents a ventral tibial spination with 3-3 spines on the right and 3-2 on the left leg I ( Figs 10D–E View FIGURE 10 ). Likewise, almost all specimens of M. dacetonoides View in CoL comb. nov. have translucent-white coxa II, except the female holotype and two additional female specimens (MZUSP-7779 cited above and MNRJ-07601, from Bahia state, northeastern Brazil), in which that coxa is darker, with only the proximal region white ( Figs 9E View FIGURE 9 , 10C View FIGURE 10 ). The vial MZUSP-7779 also contains a male with translucent-white coxae II and tibia I with 3-2 spines. Since both tibia I spination patterns were observed to occur in the same individual and both coxae II patterns can occur in the same population (with the dark coxae II pattern apparently occurring only in females), these variations are here considered as intraspecific. Therefore, M. iguazu View in CoL is here considered as a junior synonym of M. dacetonoides View in CoL comb. nov.. Similar variations in coxal coloration are also observed in M. tahyinandu View in CoL and M. atratoides spec. nov. Both types of M. dacetonoides View in CoL comb. nov. and M. iguazu View in CoL syn. nov. bear rows of robust hairs on the tibiae and metatarsi of leg IV, differing in the density of these hairs, as the former appears to have fewer of these hairs than the latter. Significantly, the male holotype of M. iguazu View in CoL (MACN- AR-19708) has fewer hairs on leg IV than the female paratype (MACN-AR-19709) ( Figs 11B, E View FIGURE 11 ). We consider this difference to be an artifact of different preservation conditions of these specimens, since the female specimen MZUSP-7779, with all coxae dark, has the dense hairs on leg IV preserved ( Fig. 10A View FIGURE 10 ). Regardless the density of these modified hairs, its mere presence on tibia and metatarsus, as well the slight lateral depression of these segments, could prove to be a further diagnostic character for M. dacetonoides View in CoL comb. nov. The variation observed in both coxae coloration and in the leg spination and hair covering suggests this species as an interesting subject for future phylogeographic studies.
Diagnosis. Males of Myrmecotypus dacetonoides comb. nov. resemble M. pilosus by the coxae II translucent white ( Fig. 11C, D View FIGURE 11 ), but they differ by the presence of a RTA, sperm duct long, five-folded, embolus short, with proximal area wider than the distal ( Figs 11G, H View FIGURE 11 , 12K, L View FIGURE 12 ) vs. RTA present, sperm duct short, with one fold, and embolus long, with the proximal area as narrow as the distal ( Reiskind 1969: fig. 247); females differ from those of M. pilosus by the V-shaped epigynal transverse ridge, placed medially on the epigynal surface ( Figs 11I View FIGURE 11 , 12M View FIGURE 12 ), whereas the epigynal transverse ridge is sinuous in M. pilosus ( Reiskind 1969: fig. 245).
Description. Male (UFMG-5538). Total length 6.83. Carapace 3.75 long, 1.57 wide. Sternum 1.74 long, 0.83 wide. Abdomen 2.66 long, 1.77 wide. Eye diameters: AME 0.13, ALE 0.07, PME 0.07, PLE 0.08. Eye inter-distances: AME-AME 0.15, AME-ALE 0.04, ALE-PLE 0.18, PME-PME 0.27, PME-PLE 0.18, AME-PME 0.16. Carapace brownish-black, somewhat narrowed in head region, with moderate constriction in cephalic region, anterior margin truncated. Feathery hairs cover carapace. Endites and labium brownish-black, prolateral margin yellowish. Chelicerae brown, two promarginal teeth of different sizes and two retromarginal teeth equal. Sternum brownish-black, shield-shaped and covered in sparse feathery hairs ( Fig. 12A–C View FIGURE 12 ). Abdomen with dorsal scute brownish-black, covered by feathery and long hairs, ventral scute brownish-black, quadrangular-shaped and tracheal scute brownish-black ( Figs 12A–B View FIGURE 12 ). Coxae II translucent white, the rest black. Trochanters following pattern of coxae, femora I and II white, with one black ventrolateral longitudinal line and dorsal surface with medial black line tapering distally, patellae, tibiae and metatarsi yellow, with black pro- and retrolateral lines. Tarsus I brown and II yellow. Legs III and IV with femora, tibiae and metatarsi brownish-black, patellae yellow with dorsal surface brownish-black, tarsi yellow. Leg IV with row of robust hairs ( Fig. 11B View FIGURE 11 ). Leg measurements: I—femur 1.84 / tibia 1.90 / metatarsus 1.44; II—femur 1.71 / tibia 1.63 / metatarsus 1.48; III—femur 1.86 / tibia 1.49 / metatarsus 1.63; IV—femur 3.13 / tibia 2.42 / metatarsus 2.48. Spination: I-femur do 1-0-1-1, pl 0-0-0-1; tibia ve 2-2-2 (3-3); metatarsus ve 2-2/ II-femur do 1-0-1-1, pl 0-1-0-1, rl 0-1-0-1; tibia ve 2-2; metatarsus ve 2-2/ III-femur do 0-0-1-1; pl 0-1-1, rl 0-1-1; tibia do 0-0-1, pl 0-1-1, rl 0-1-1, ve 2-2; metatarsus pl 1-1-0-1, rl 1-1-0-1, ve 2-2-2-1/ IV-femur do 1-0-1-1, pl 0-0-0-1, rl 0-0-0-1; tibia do 0-0-1, pl 1-0-1, rl 1-0-1, ve p 1-0-1; metatarsus pl 1-1-0-1, rl 1-1-0-1, ve 2-2. Tibia with proximal area blunt, with small spiniform RTA. Palp with globose genital bulb drawn into long neck with twisted end, embolus short and sclerotized, wide, tip smooth ( Figs 11G, H View FIGURE 11 , 12K, L View FIGURE 12 ).
Female (UFMG-320). Total length 8.93. Carapace 4.79 long, 2.00 wide. Sternum 2.22 long, 1.57 wide. Abdomen 3.56 long, 2.86 wide. Eye diameters: AME 0.12, ALE 0.03, PME 0.07, PLE 0.06. Eye inter-distances: AME-AME 0.12, AME-ALE 0.04, ALE-PLE 0.17, PME-PME 0.26, PME-PLE 0.16, AME-PME 0.17. Carapace, as in male. Endites and labium brownish-black. Chelicerae brown, two promarginal teeth of different sizes and two retromarginal teeth equal and equidistant. Sternum brownish-black, shield-shaped, covered in sparse feathery hairs ( Fig. 12D–F View FIGURE 12 , 13F–H View FIGURE 13 ). Abdomen globose, with moderately small, brownish-black dorsal scute, golden and feathery hairs covering abdomen, as in male ( Fig. 11F View FIGURE 11 ). Coxae II translucent white. Leg measurements: I—femur 2.40 / tibia 2.36 / metatarsus 1.66; II—femur 2.36 / tibia 2.34 / metatarsus 1.65; III—femur 2.31 / tibia 1.89 / metatarsus 1.82; IV—femur 4.01 / tibia 1.62 / metatarsus 1.68. Spination: I-femur do 1-0-0-1, pl 0-0-0-1; tibia ve 1p-2-2 (3-2); metatarsus ve 2-2/ II-femur do 1-0-1-1, pl 0-1-0-1, rl 0-1-0-1; tibia ve 2-2; metatarsus ve 2-2/ III-femur do 0-0-1-1; pl 0-1-1, rl 0-1-1; tibia do 0-0-1, pl 0-1-1, rl 0-1-1, ve 2-2; metatarsus pl 1-1-0-1, rl 1-1-0-1, ve 2-2-2-1/ IV-femur do 1-0-1-1, pl 0-0-0-1, rl 0-0-0-1; tibia do 0-0-1, pl 1-0-1, rl 1-0-1, ve p 1-0-1; metatarsus pl 1-1-0-1, rl 1-1-0-1, ve 2-2. Epigyne with V-shaped epigynal transverse ridge, copulatory openings small, laterally oriented. Vulva with small globose spermathecae followed by short neck. Copulatory ducts hidden under STII ( Figs 11J View FIGURE 11 , 12M, N View FIGURE 12 ).
Variation. Rubio & Arbino (2009) documented variation in the refractory pubescence of the carapace and abdomen, which can be gray or golden. In addition, variation in the coxa II coloration of females (dark or completely translucent) is reported here, as well as variation in the ventral spination of tibia I (3-3 or 3-2) in both sexes ( Figs 9E View FIGURE 9 , 10C View FIGURE 10 , 11F View FIGURE 11 , 12H View FIGURE 12 ).
New records. BRAZIL: Amazonas: Manaus, Lago do José [04°05’43.0’’S, 41°43’51.6’’W], 1♂, 9.VIII.1978, J. Adis leg. ( IBSP, IB-17089 ); Manaus , Estação Experimental de Silvicultura Tropical , 02°37’S, 60°02’’W, 1♀, 11.VIII.1980, P.S. Oliveira leg. (IBSP-151321) GoogleMaps ; Pará: Benevides [03°02’01.0’’S, 59°58’56.1W’ ’], 1♂, 18–22. III GoogleMaps , D.R. Santos-Souza leg. ( MPEG ( ARA)-003136); Gurupi, Rio Gurupi [17°53’41.5’’S, 51°43’41.4’’W], 1♂, V GoogleMaps .1963, B. Malkin leg. (MZUSP-3297); Mato Grosso: Chapada dos Guimarães, 1♂, 12.VII. 2011, R .C. Francisco leg. (MCTP-34445); Tocantins: Sandolândia, Margem Direito do Rio Araguaia , 12°15’S, 50°07W, 1♂, 5–13.VII.1997, L.S. Rocha leg. ( IBSP, IB-12014 ) GoogleMaps ; Bahia: Prado, Fazenda Furado , 1♀, 12.IX.1970 (MNRJ-07601) ; Goiás: Jataí [01°22’27.2’’S, 48°15’45.9’’W], 1♂, 1995, Carrera leg. (MZUSP-4338) GoogleMaps ; Minas Gerais: Presidente de Morais, Fazendo do Sapé, rodovia MG-424, 19°28’06.18’’S, 44°14’29.78’’W, 1♀, 1.XII.2000, E.S.S. Álvares leg. (UFMG-320); São Lourenço [22°07’30.7’’S, 39°45’33.2’’W], 1♀, 14–17.XI.2009, M.A. Ulyssia & F.F. Alberto leg. (IBSP-156967); Lagra Santa [19°32’48.3’’S, 43°58’30.2’’W], 1♂, 26.XI.1960, B. Malkin leg. (MZUSP-7961) GoogleMaps ; São Paulo: Caraguatatuba [23°37′13’’S, 45°24′47’’W], 1♂ 1♀, 29. III GoogleMaps .1962, C.D.Z. leg. (MZUSP- 7779); Rio de Janeiro: Itamaraju [17°02’08.9’’S, 39°45’33.2’’W], 1♂, 22.XII.1969, (MNRJ-07600) GoogleMaps ; Rio Grande do Sul: Machadinho, 10 km before Machadinho Dam , 27º29’42’’S, 51°48’57’’W, 1♂, 5.II.2008, M.O. Gonzaga & A.J. Santos leg. (UFMG-5538) GoogleMaps .
Distribution. South America ( Fig. 26 View FIGURE 26 )
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 |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |
Myrmecotypus dacetonoides ( Mello-Leitão, 1948 )
Silva-Junior, Cláudio J. & Bonaldo, Alexandre B. 2024 |
Apochinomma dacetonoides Mello-Leitão, 1948: 182
Mello-Leitao, C. F. de 1948: 182 |