Agaporomorphus tortus, Miller, 2020
publication ID |
https://dx.doi.org/10.3897/zookeys.923.48337 |
publication LSID |
lsid:zoobank.org:pub:8DB62739-6222-4331-AF37-9DC676B12FC6 |
persistent identifier |
https://treatment.plazi.org/id/8FA75E35-E24C-47D5-9E82-939597462D54 |
taxon LSID |
lsid:zoobank.org:act:8FA75E35-E24C-47D5-9E82-939597462D54 |
treatment provided by |
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scientific name |
Agaporomorphus tortus |
status |
sp. nov. |
Agaporomorphus tortus View in CoL sp. nov. Figures 4-6 View Figures 1–6 , 16 View Figures 16–23 , 17 View Figures 16–23 , 24 View Figures 24, 25 , 26 View Figure 26
Type locality.
Suriname, Sipaliwini District, Sipaliwini Savannah Nature Reserve, Four Brothers Mountains, 2°00.656'N, 55°59.070'W, 275 m.
Diagnosis.
This species is in the A. dolichodactylus species group which lacks characteristics of other species groups such as expanded male antennomeres, setae on the dorsal surface of the male median lobe, or stridulatory structures or triangular processes on the abdomen ( Miller 2005). Like certain other members of the A. dolichodactylus species group, A. tortus has similar male genitalia (Figs 4 View Figures 1–6 - 15 View Figures 7–15 ) including an elongate process on the basal, dorsal surface of the male median lobe (Fig. 4 View Figures 1–6 ), a lobe at the end of male mesotarsomere V (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ), and elongate and somewhat sinuate male mesotarsal claws (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ). From other species in the group this species differs in the shape of the male median lobe which is deeply asymmetrically emarginate apically in ventral aspect (Fig. 5 View Figures 1–6 ) and with other distinctive shapes (Figs 4 View Figures 1–6 , 5 View Figures 1–6 ).
Description.
Measurements (N = 3). TL = 3.0-3.2 mm, GW = 1.5 mm, PW = 1.2-1.3 mm, HW = 0.8-0.9 mm, EW = 0.5 mm, FL = 0.7-0.8 mm, FW = 0.2-0.3 mm, TL/GW = 2.0-2.2, HW/EW = 1.6-1.7, FL/FW = 2.9-3.6. Body shape elongate oval, evenly and shallowly curved along lateral margins, curvature continuous between pronotum and elytron.
Coloration. Head, pronotum and elytron orange, similar in coloration throughout dorsal surface. Ventral surface orange, similar in coloration throughout but legs slightly lighter in color.
Sculpture and structure. Head shiny, very finely microreticulate comprised of small isodiametric cells; eyes moderately large (HW/EW = 1.6-1.7). Pronotum shiny, similar microreticulation to head; lateral margin slightly curved, extremely finely beaded, bead absent at anterior angle. Elytron with lateral margin shallowly curved; surface shiny, microreticulation extremely fine, apical half with numerous extremely fine punctures. Prosternum elongate, carinate, prosternal process short, strongly carinate medially. Metaventer and metaventral wings smooth and shiny, with very dense, fine microreticulation. Metacoxa smooth and shiny, similar in microsculpture to metaventer; metacoxal lines distinct, region between metacoxal lines narrow medially; metafemur not unusually broadened (FL/FW = 2.9-3.6).
Male genitalia. Median lobe complex in shape, asymmetrical; in lateral aspect narrow basally, broadened apically, apically broadly truncate with medial small lobe extending beyond truncation (Fig. 4 View Figures 1–6 ); in ventral aspect broad apically, with complex arrangement of lobes and flanges, apicomedially with large, asymmetrical excavation between surfaces and distinctive deep apical emargination on left side of middle (Fig. 5 View Figures 1–6 ); lateral lobe in lateral aspect robust basally, apically slender, with long, slender apical lobe, with long series of setae along dorsal margin (Fig. 6 View Figures 1–6 ).
Sexual dimorphism. Males protarsomeres I-III distinctly broader than in females with four large adhesive setae; females without expansion or adhesive setae. Male mesotarsomeres I-III broader than in females, not as strongly expanded as male protarsomeres I-III, male mesotarsomeres with four large ventral adhesives setae; apex of mesotarsomere V extended into small lobe on posterior margin of apex (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ), mesotarsal claws of male elongate, slightly sinuate (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ); females without these mesoleg modifications.
Variation. There is some minor variation in intensity of coloration of the dorsal surface between specimens but this may be because some specimens are more teneral than others.
Distribution.
This species is only known from southern Suriname (Fig. 24 View Figures 24, 25 ).
Habitat.
The type series was collected from "vegetated pools in savanna."
Discussion.
This species belongs to the A. dolichodactylus group of Agaporomorphus of Miller (2005), and specifically close to A. dolichodactylus and A. mecolobus (Fig. 26 View Figure 26 , see below) based on the presence of a long lobe basally on the dorsal margin of the male median lobe (Fig. 4 View Figures 1–6 ), a distinctive lobe on the apex of the male mesotarsomere V (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ), and male mesotarsal claws long and sinuate (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ). This is the first of the group known from northern South America (Fig. 24 View Figures 24, 25 ) with the other species in Brazil and Peru.
Etymology.
This species is named tortus , Latin for “twisted” for the complex shape of the male median lobe in this species (Figs 4 View Figures 1–6 , 5 View Figures 1–6 ).
Type material.
Holotype in NZCS, male labeled, "Suriname: Sipaliwini District Sipaliwini Savanna Nature Res. 2°00.656'N, 55°59.070'W, 275 m vegetated pools in savanna 1.iv.2017; leg. A.E.Z. Short SR17-0401-01A/ SEMC1542796 KUNHM-ENT [barcode label]/ Holotype Agaporomorphus tortus Miller, 2020 [red label with double black line border]." 2 paratypes labeled same as holotype except [ …SEMC1542807…] and [ …SEMC1516119…] and paratype label, “… Paratype Agaporomorphus tortus Miller, 2020 [blue label with black line border]."
Phylogenetic results.
The parsimony analysis resulted in two equally parsimonious trees (L = 17, CI = 82, RI = 92) (Fig. 26 View Figure 26 ). The trees comport well with previous results ( Miller 2001; 2005; Miller and Wheeler 2008; Miller 2014) with three main clades characterized by specific distinctive synapomorphies. These correspond to the A. dolichodactylus -, A. knischi -, and A. pereirai groups of Miller (2001) with the exception of the new species A. hamatocoles (described above) which has an unresolved position in the tree because of absence of the synapomorphies shared among the other clades in the phylogeny (Fig. 26 View Figure 26 ). The only difference between the trees is a rearrangement within the A. knischi clade (Fig. 26 View Figure 26 ). The other new species, A. tortus , is resolved with the A. dolichodactylus clade based on presence of an elongate lobe on the dorsal base of the male median lobe (Figs 4 View Figures 1–6 , 19 View Figures 16–23 , 13 View Figures 7–15 , shorter and broadly rounded in A. grandisinuatus , Fig. 7 View Figures 7–15 ). Specimens also have long, somewhat sinuate mesotarsal claws with a distinct lobe at the apex of mesotarsomere V (Figs 16 View Figures 16–23 , 17 View Figures 16–23 ) (synapomorphy with A. dolichodactylus (Figs 20 View Figures 16–23 , 21 View Figures 16–23 ) and A. mecolobus (Figs 22 View Figures 16–23 , 23 View Figures 16–23 ) and a very long apical lobe on the male lateral lobe (Fig. 6 View Figures 1–6 ), shared with other members of the A. dolichodactylus clade (Figs 9 View Figures 7–15 , 12 View Figures 7–15 , 15 View Figures 7–15 ).
New records of other species of Agaporomorphus
A. colberti Miller and Wheeler (Fig. 24 View Figures 24, 25 ). Suriname, Sipaliwini District, 3°47.479'N, 56°08.968'W, 320m, CSNR, nr Kappel airstrip, forest pools near Petromia Falls, 13 Aug 2013, Short, Bloom and Kadosoe, legs, SR13-0813-03A (3, KUNHM; SEMC1235490, SEMC1234094, SEMC1234095); Sipaliwini District, 3°47.479'N, 56°08.968'W, 320m, CSNR, nr Kappel airstrip, forested stream and stream pools, 24 Aug 2013, Short and Bloom, legs, SR13-0824-03A (2, KUNHM; SEMC1234951, SEMC0966126); Sipaliwini Dist, 3°55.600'N, 56°11.300'W, 600m, CSNR, Tafelberg Summit, nr Augustus Cr. Camp, pond on trail into Arrowhead basin, 16 Aug 2013, Short and Bloom, legs, SR13-0816-02A (A1, KUNHM: SEMC0930616).
These are the first records of A. colberti from Suriname with previous records from Venezuela ( Miller and Wheeler 2008: fig. 24).
A. pereirai Guignot (Fig. 25 View Figures 24, 25 ). Suriname, Sipaliwini Dist, 3°55.600'N, 56°11.300'W, 600m, CSNR, Tafelberg Summit, nr Augustus Cr. Camp, pond on trail into Arrowhead basin, 17 Aug 2013, Short and Bloom, legs, SR13-0817-01A (1, KUNHM: SEMC0965435, SEMC0965426, SEMC0965425, SEMC0965396, SEMC0965397); Sipaliwini Dist., 2°00.526'N, 55°58.572'W, 292m, Sipaliwini Savanna Nature Res, side pools of small clearwater stream in savannah, 20 Mar 2017, Short and Baca, legs, SR17-0330-02B (2, KUNHM; SEMC1541937, SEMC1541940); Sipaliwini Dist, 3°53.942'N, 56°10.849'W, 733m, SCNR, Tafelberg Summit, nr Caiman Cr camp, forest detrital pools, 19 Aug 2013, Short and Bloom, legs, SR13-0819-02A (1, KUNHM; SEMC0966170).
Previous records of this species are from Suriname (Cottica River, Moengo, Boven: fig. 25), and Matto-Grosso and Para, Brazil ( Guignot 1957; Miller 2001).
Species list of the genus Agaporomorphus
Agaporomorphus knischi species group
A. colberti Miller & Wheeler, 2008. Venezuela, Suriname
A. julianeae Hendrich, Apenborn, Burmeister, & Balke, 2013. Peru
A. knischi Zimmermann, 1921. Brazil, Peru, Bolivia
A. sharynae Miller, 2014. Venezuela
A. silvaticus Miller, 2005. Peru
A. tambopatensis Miller, 2005. Peru
Agaporomorphus dolichodactylus species group
A. dolichodactylus Miller, 2001. Brazil, Bolivia
A. grandisinuatus Miller, 2001. Brazil, Peru
A. mecolobus Miller, 2001. Brazil
A. tortus sp. nov. Suriname
Agaporomorphus hamatocoles species group
A. hamatocoles sp. nov. Suriname
Agaporomorphus pereirai species group
A. pereirai Guignot, 1957. Brazil, Suriname
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Copelatinae |
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