Tonnoiriella veronikae, Ježek, Jan & Oboňa, Jozef, 2016

Ježek, Jan & Oboňa, Jozef, 2016, escriptions of two new species of Afrotropical Psychodidae (Diptera), Zootaxa 4144 (4), pp. 515-528 : 520-526

publication ID

https://doi.org/ 10.11646/zootaxa.4144.4.4

publication LSID

lsid:zoobank.org:pub:00F4A4CE-5782-49F6-97B6-A37AAFA5C747

DOI

https://doi.org/10.5281/zenodo.5620484

persistent identifier

https://treatment.plazi.org/id/7844F65C-FFB2-FF81-6E8E-1120B892BCD6

treatment provided by

Plazi

scientific name

Tonnoiriella veronikae
status

sp. nov.

Tonnoiriella veronikae View in CoL sp. nov.

( Figs 19–35 View FIGURES 19 – 24 View FIGURES 25 – 30 View FIGURES 31 – 35 )

Type material. Holotype ♂: Madagascar, Toamasina prov., Analamazaotra 1.4 km SSW Andasibe vill. (Périnet), cca 940 m a.s.l., 48° 24' 48'' E, 18° 56' 09'' S, S on the first place (see N. nyahururuensis ) 20.i.2000, P. Chvojka leg. Slide with a dissected specimen, Cat. No. 34699, Inv. No. 22010 ( NMPC). GoogleMaps

Paratypes 2 ♂ (slides, NMPC): The same locality, date and collector, Cat. No. 34700–34701, Inv. No. 22011– 22012 ( NMPC). All material P. Chvojka leg. (by sweep netting).

Type locality. Madagascar: Toamasina prov., Analamazaotra 1.4 km SSW Andasibe vill. (Périnet).

Etymology. The new species name (adjective) is based on the first name of the granddaughter of the first author: Veronika Tomková.

Bionomics. Unknown. Adults were collected in secondary forest habitat, specifically a swampy area with a nearby rill.

Distribution. Currently known only from Madagascar.

Description. Male. Head 0.95 times as long as broad ( Fig. 19 View FIGURES 19 – 24 ). Vertex inflated dorsally, frons with numerous setae alveoli in a stripe, divided and divergent both near vertex and near frontal suture, sometimes hardly divided in the vertical axis, sparse on both sides of head margins ( Fig. 19 View FIGURES 19 – 24 ). Eye bridge is moderately developed, of three complete facet rows ( Fig. 31 View FIGURES 31 – 35 ), upper apices of eyes tapered medially. Eyes separated by about three facet diameters, connected by arched interocular suture, a little strengthened laterally, sometimes interrupted medially ( Fig. 31 View FIGURES 31 – 35 ), with a few postocular bristles (4–6). Setae alveoli of frontoclypeus arranged in a strangulated triangular central scar patch near basis of antennae tapering to a tongue-shaped area below frontal suture. Ratio of distances of apices of eyes (tangential points) to minimum width of frons approximately 2.5:1. Antennae ( Figs 25 View FIGURES 25 – 30 , 32 View FIGURES 31 – 35 ) with 16 articles. Scape slender basally, pedicel almost ball-shaped, 1.5 times as long as scape. Scales of pedicel broadly lanced in contrast to stiletto-shaped scales of fagellomeres. Flagellomeres mostly spindle-shaped, however the last three flagellomeres a little reduced in size (cask-shaped or ovoid). Antennomere 14 with a hemispherical axial apiculus. Sensory filaments (ascoids) nedle-shaped, bent, paired, 2.8 times shorter than the flagellomeres bearing them. Mouthparts extending beyond basal palp segments. Length ratio of maxillary palps 1.0:2.0:2.1:3.8, the last segment is annulate, connected somewhat subapically with preceding one ( Fig. 20 View FIGURES 19 – 24 ). For the terminal lobes of labium, as shown in Fig. 33 View FIGURES 31 – 35 , the lines of spines between both lobes are not developed. Ratio of maximum length of cibarium ( Figs 19 View FIGURES 19 – 24 , 26 View FIGURES 25 – 30 ) to length of epipharynx 1.7:1, labrum with microsetae.

Thorax with mesothoracic allurement protuberance almost flattened, with a circular thoracic spiracle anteriorly, anepisternum with a triangular setose patch ( Fig. 21 View FIGURES 19 – 24 ). Wings ( Fig. 34 View FIGURES 31 – 35 ) 1.6 mm long - holotype, both paratypes 1.5 mm, well sclerotised, lancet-shaped, not enlarged in anal and humeral areas, with rounded top, clear, wing membrane bare. Basal costal nodes distinct, Sc straight, uninterrupted. Medial fork incomplete in contrast to radial one. R5 ends beyond wing apex. Bases of M3, CuA1 and CuA2 are not connected. The ratio of maximum wing length to maximum of width 2.7:1. Strengthened veins: Sc (thickened basally), whole R2 and R5, all veins distally, however, R4 and M1 stout also in basal cell, CuA1 as well distally and basally with a declined turn. CuA2 strongly thickened and arched at basis, gradually tapering distally. Halteres ( Fig. 27 View FIGURES 25 – 30 ) have a prolonged stem and ovate knob with a row of minute hairs laterally. Ratio of maximum length of halteres to their maximum width approximately 2.6:1. Length ratios of femora, tibiae and first tarsal segments: P1 1.9:2.0:1.0, P2 1.9:2.5:1.2, P3 2.0:2.8:1.2. Claws of P1 bulbose at base, bent, haired in two basal thirds, as shown in Fig. 28 View FIGURES 25 – 30 , twice pointed, subapical tooth is blunt in contrast to the sharp prolonged terminal spike.

Male genitalia with ejaculatory apodeme straight in dorsal view, almost parallel-sided distally with an ovoid chamber, widened proximally in convergent margins, terminating anteriorly in a sclerotized axial rim ( Fig. 30 View FIGURES 25 – 30 ), compressed dorso-ventrally and bent from lateral view ( Fig. 24 View FIGURES 19 – 24 ). Aedeagal complex asymmetrical, wrinkled basally ( Figs 24 View FIGURES 19 – 24 , 30 View FIGURES 25 – 30 ), distal part with a boomerang or sickle-shaped paramere, laterally with a cut side arch without a bulbous protuberance, superficial spines quite missing. Gonocoxites almost cylindrical ( Figs 23 View FIGURES 19 – 24 , 30 View FIGURES 25 – 30 ), with a stout seta on inner side basally and 2–3 small setae near distal part of the ejaculatory apodeme. Gonocoxal apodemes forming a pair of rectangular projections anteriorly ( Fig. 30 View FIGURES 25 – 30 ). Gonostyli conical, not gradually tapering, with a small swelling in the middle, hooked terminally. Length ratio of ejaculatory apodeme and gonostylus approximately 1.3:1. Epandrium ( Figs 29 View FIGURES 25 – 30 , 35 View FIGURES 31 – 35 ) almost bare, with two patches of scanty latero-caudal hair insertions. Basal paired apertures almost elliptical, not connected, developed in a proximal small dark area of epandrium. Remainders of ventral plate missing. Hypandrium ( Figs 22 View FIGURES 19 – 24 , 30 View FIGURES 25 – 30 ) narrow, triangular in the middle, conspicuously strangulated subapically, hemicircular terminally. Epiproct lobule-shaped, featureless ( Fig. 35 View FIGURES 31 – 35 ), hypoproct ( Figs 29 View FIGURES 25 – 30 , 35 View FIGURES 31 – 35 ) narrowed proximally, rounded distally, both parts haired. Epandrial clasping lobes slightly C-shaped ( Fig. 35 View FIGURES 31 – 35 ), almost cylindrical, only a little widened basally ( Figs 29 View FIGURES 25 – 30 , 35 View FIGURES 31 – 35 ), with five not frazzled tenacula subapically, as a fraction of surstylus (1.5:1).

Female. Unknown.

Differential diagnosis. The Afrotropical species of genus Tonnoiriella are morphologically rather uniform, except for the male genitalia (see Table 2 View TABLE 2 ). T. veronikae sp. nov. described here is very similar to T. drepanopenis ( Duckhouse, 1975) , which has relative lengths of three first antennomeres 1.4:1.7:1.0, relative lengths of palpal segments 1.0:1.1:1.2:2.5, hypandrium in the middle triangular, rounded terminally, caudal sclerite of aedeagal complex boomerang-shaped, distal margin of caudal sclerite arched horizontally, gonostyli gradually tapering and apex of gonostylus rounded. On the other hand T. veronikae sp. nov. differs by the relative length of antennomeres 1–3 1.2:1.3:1.0, relative length of palpal segments 1.0:1.7:1.8:3.2, hypandrium almost triangular in the middle, strangulated subapically, semicircular terminally, caudal sclerite of aedeagal complex almost boomerang-shaped, but with cut side arch, distal margin of caudal sclerite approximately straight horizontally, gonostyli not gradually tapering, with a small swelling in the middle, apex of gonostylus conspicuously hooky.

cracens drepanopenis fasciola stuckenbergi veronikae Comments. Wagner (1978, 1990 View in CoL , 1994) and Wagner & Salamanna (1984) included Neoarisemus View in CoL in tribe Brunettiini; Vaillant (1982b, 1986, 1990), Wagner (1997a, b) and Quate & Brown (2004) placed it in Setomimini and Ježek (2004) in Mormiini (Brunettiina). Moreover, Duckhouse (1987) placed Neoarisemus in Maruinini View in CoL , as followed by Kvifte (2012).

A tribal placement of Tonnoiriella View in CoL was historically contraversial as well. Vaillant (1971, 1982a), Duckhouse (1975), Wagner & Salamanna (1984), Wagner (1979, 1987, 1990) and Ježek (1999) placed this genus in Pericomaini, Vaillant (1982b) and Wagner (1997a, b) in Setomimini and Duckhouse (1987), Wagner & Andersen (2007), Kvifte et al. (2011), Kvifte (2012) and Afzan & Belqat (2016) in Maruinini.

Duckhouse (1987) considered both Neoarisemus and Tonnoiriella in Maruinini by the anterior plate-like gonocoxal condyles and dorsoventral ejaculatory apodeme, radial wing fork before medial one, R2 is several times longer than R2+3, flagellomeres are barrell-shaped and narrower than scpe and pedicel. We follow here Duckhouse´s opinion in concordance with Kvifte (2012), however, Duckhouse (1991) additionally concluded that Maruinini are probably paraphyletic; ultimately, molecular evidence may be necessary to accurately resolve the placement of Neoarisemus and Tonnoiriella as well as future exact modern study.

TABLE 2. Comparison of diagnostic characters for males of five Afrotropical Tonnoiriella species.

dorsal apices of rounded eyes rounded conspicuously pointed rounded rounded
relative length of 1.2:1.5:1.0 the first three antennal articles 1.4:1.7:1.0 1.0:1.4:1.2 1.1:1.3:1.0 1.2:1.3:1.0
relative length of 1.0:1.4:1.5: palpal segments 2.8 1.0:1.1:1.2: 2.5 1.1:1.0:1.6: 2.0 1.0:1.1:1.1: 2.3 1.0:1.7:1.8: 3.2
hypandrium on with parallel- posterior margin in sided tongue- the middle shaped enlargement, rounded terminally triangular, with rounded prong stripe -shaped, narrow, not widened conspicuously widened, oblong - shaped triangular, constricted subapically, semicircular terminally
base of gonocoxite bare on inner side setose bare bare setose
gonostylitapering gradually gradually gradually gradually abruptly,with a small swelling in the middle
apex of gonostylus slightly hooked slightly hooked slightly hooked blunt (cut) conspicuously hooked
caudal sclerite of y - shaped aedeagal complex laterally on left side boomerang - shaped ice -axe -shaped laterally on right side resembling the cross -section of a mushroom, distinctly broader than high almost boomerang - shaped, but with left side arch cut
distal margin of nearly straight caudal sclerite of aedeagal complex horizontally arched arched straight nearly straight
number of tenacula five five four five five
NMPC

National Museum Prague

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Diptera

Family

Psychodidae

Genus

Tonnoiriella

Loc

Tonnoiriella veronikae

Ježek, Jan & Oboňa, Jozef 2016
2016
Loc

veronikae

Comments. Wagner 1978
1978
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