Tarchonanthogethes Audisio & Cline, 2009
publication ID |
https://doi.org/ 10.5281/zenodo.5319334 |
persistent identifier |
https://treatment.plazi.org/id/03BE87CC-F608-FFE1-BA69-FF2FFD6CFC0C |
treatment provided by |
Felipe |
scientific name |
Tarchonanthogethes Audisio & Cline |
status |
gen. nov. |
27. Tarchonanthogethes Audisio & Cline , gen. nov.
( Figs. 27 a–k View Fig )
Type species. Pria martini Grouvelle, 1899: 147 , 148 (partim), nec Anthystrix martini sensu KIREJTSHUK & EASTON (1988) : 42, 46 (partim) (by present designation) [= Tarchonanthogethes martini (Grouvelle, 1899) comb. nov.]. See AUDISIO et al. (2009a).
Generic description and diagnosis. Inclusive species vary greatly in size (1.6–2.7 mm length), and share the following combination of characters.
Body color and pubescence: pubescence variable, usually long, golden to silvery-whitish and dense, recumbent, partially obscuring the predominantly orange-brown dorsal body surface; pronotal and elytral sides flattened and usually paler than disc ( Fig. 27a View Fig ); a few isolated species possess much finer and shorter pubescence, not obscuring the dorsal body surface ( Fig. 27b View Fig ); lateral margin of pronotum and elytra with a series of faintly distinct, small and short setae, each seta 0.3–0.5× as long as those on elytral disc; posterior margin of pronotum with relatively short, distally multifid microsetae, microsetae also on middle portion anterior to scutellum ( Fig. 27f View Fig ).
Dorsal habitus: body moderately convex, oval ( Figs. 27a, b View Fig ); dorsal punctures on discal portion of pronotum as large as or larger than eye facet, moderately to deeply impressed ( Figs. 27a, b View Fig ); anterior margin of clypeus truncate to slightly emarginate medially, simple, without small distinct medial bulge, and more or less distinctly bordered ( Figs. 27a, b, i View Fig ); circum-ocular furrows (occipital sulci) on head deeply impressed and complete ( Fig. 27i View Fig ); eyes large and usually markedly projecting laterally ( Figs. 27a, b View Fig ); posterior angles of pronotum distinct, blunt, obtuse ( Figs. 27a, b View Fig ), never directed posteriorly; scutellum uniformly punctured on most of exposed portion ( Fig. 27f View Fig ); elytra with strongly variable punctation, normal and not transversely strigose, or confusedly orange peel-like sculpturing, or finely and completely transversely strigose sculpturing; elytral humeral angle distinct, broadly obtuse, never laterally protruding ( Figs. 27a, b View Fig ); elytral humeral striae not distinct; elytral pre-sutural striae faintly visible, originating at scutellar vertex or slightly posterior, terminating at elytral apex, and delimiting on each elytron a faintly distinct, flat, unraised sutural border, more distinct at distal fourth, distinctly narrower than proximal width of 3 rd antennomere; elytral apices truncately rounded in both sexes ( Fig. 27a View Fig ), only the isolated T. rotundiclava possesses elytra faintly obtusely lobed posteriorly in females; pygidium partially exposed, moderately convex, apically rounded in both sexes ( Figs. 27a, b View Fig ).
Ventral habitus: antennal furrows markedly delimited, and moderately convergent posteriorly or nearly subparallel; mentum subpentagonal ( Fig. 27g View Fig ); prosternal antennal furrows on anterior margin of prosternum strongly delimited and raised, moderately divergent, never extending posteriorly to anterior margin of procoxal cavity ( Fig. 27g View Fig ); prosternal process variably shaped, moderately to markedly wide, subapical portion 2.0–2.7× as wide as maximum width of 1 st antennomere, apex usually bluntly rounded ( Fig. 27g View Fig ); lateral borders of prosternal process delimiting deeply impressed and distinct furrows, distally terminating over predistal lateral expansions ( Fig. 27g View Fig ); posterior margin of mesoventrite simple, never medially incised; scarce sexual dimorphism expressed in male impressions on metaventrite; first two visible abdominal ventrites simple in both sexes, without tufts of setae; caudal marginal lines of metacoxal cavities simple, subparallel and contiguous to posterior margin of metacoxal cavities, with moderately deep arched impression of outer ‘axillary’ line; ‘axillary’ space on first abdominal ventrite moderately developed, ‘axillary’ angle more or less obtuse; strongly marked and deeply impressed arched impressions on basal portion of last visible abdominal ventrite, usually partially covered by distal portion of penultimate visible abdominal ventrite ( Fig. 27g View Fig ).
Appendages: male 1 st antennomere 0.8–1.1× as long as width of protibiae excluding distal teeth ( Figs. 27g, h View Fig ); 3 rd antennomere 2.0–3.0× as long as wide in both sexes, distinctly longer and much thinner than 2 nd; 4 th and 5 th antennomeres usually subequal in both sexes, relatively short, moderately longer than wide ( Fig. 27h View Fig ); male and female antennal club moderately compact, nearly symmetric, comprising last 3 antennomeres, only the isolated T. rotundiclava with 4-jointed male antennal club ( Figs. 27a, h View Fig ); labial palpi relatively short in both sexes (as in Fig. 26b View Fig ), terminal segment 1.6–1.7× as long as wide; maxillary palpi relatively long and slender in both sexes (as in Fig. 26c View Fig ), terminal segment 1.8–1.9× as long as wide; mandible mid-sized, moderately short, apex bifid and moderately acuminate, no sexual dimorphsim; tarsi of normal size and shape, 0.7–0.9× as long as corresponding tibiae ( Figs. 27a, b, g View Fig ); tarsal claws simple, never toothed at base; protibiae with highly variable teeth on outer margins, simple, small and crenulate ( Fig. 27a View Fig ) to strongly developed and serrate; lateral margin of meso- and metatibiae bearing a single and regular row of long and thin, yellowish pegs ( Figs. 27a, b, g View Fig ), without U-shaped sinuosity at distal third; meso- and metatibiae triangular, of variable width, long and slender to subtrapezoidal; usually scarce sexual dimorphism in tibial shape; tarsal plates of prolegs wider in males; posterior margin of metafemora simple in both sexes, without tubercles or projections.
Male genitalia: tegmen variably shaped, usually without processes along inner side of parameres ( Fig. 27c View Fig ; Plate 2, Figs. 7–8 View Fig View Fig , 10–11 View Fig View Fig , 13–14 View Fig View Fig , 16– 17 View Fig View Fig in KIREJTSHUK & EASTON 1988), and without deep median longitudinal desclerotization from proximal portion of tegmen extending to medial distal V-shaped excision; median lobe of aedeagus variably shaped, without lateral emargination, apex variable ( Fig. 27d View Fig ); main sclerites of internal sac (flagellum) usually large, markedly sclerotized, ~2× shorter than aedeagus ( Fig. 27e View Fig ).
Female genitalia (ovipositor): variably shaped, usually large; styli usually long and distinct, simple, unpigmented, inserted near narrow but frequently minutely subtruncate apex of contiguous or distally narrowly divergent (known from a single case, i.e. Plate 2, Fig. 15 View Fig in KIREJTSHUK & EASTON 1988) gonostyloids, each gonostyloid usually lightly sclerotized and moderately pigmented distally, with a simple, never indentate outer portion of basicoxites ( Fig. 27k View Fig ), and a single or frequently double, pigmented and sclerotized arcuate area(s) along outer subdistal portion of gonostyloids. ‘Central point’ of ovipositor usually located more distad than middle, without proximad directed spicule.
Etymology. The generic name is derived from the host-plant tribe of all inclusive species, i.e. Tarchonantheae , and from ‘- gethes ’, to emphasize its phylogenetic relationship with Meligethes . Gender masculine.
Biology. All species are strictly associated for larval development with male inflorescences of trees and bushes of Asteraceae , within the phylogenetically isolated tribe Tarchonantheae (specifically with the genera Brachylaena R. Br. and Tarchonanthus L.) (AUDISIO et al. unpublished data).
Phylogenetic position. This genus is relatively large and heterogeneous when compared to other genera within the Anthystrix generic complex, and appears to be more closely related to Anthystrix based on some features and to Cyclogethes based on other characters. Some of the described species have been previously erroneously attributed to the more distantly related genera Meligethinus and Meligethes (see below).
Taxonomy and geographic distribution. Tarchonanthogethes gen. nov. includes 6 described species and more than 10 species awaiting formal description. The genus exhibits an expression of a transformation series involving several morphological characters, and may be separated at least into five distinct groups, i.e. the ‘ martini ’, ‘ rotundiclava’, ‘ capeneri ’, ‘ flavus ’, and ‘ singularis ’ species-groups. An upcoming paper is devoted to a complete taxonomic revision of the genus (AUDISIO et al. in prep.).
Tarchonanthogethes capeneri ( Kirejtshuk & Easton, 1988) South Africa: Limpopo, NW Province comb. nov. (from Meligethinus )
Tarchonanthogethes flavus ( Kirejtshuk & Easton, 1988) South Africa: Limpopo, NW Province comb. nov. (from Meligethinus )
Tarchonanthogethes hirtus ( Kirejtshuk & Easton, 1988) South Africa: KwaZulu-Natal, Mpumalanga comb. nov. (from Meligethinus )
Tarchonanthogethes martini (Grouvelle, 1899) South Africa: KwaZulu-Natal, Mpumalanga comb. nov.
= Pria martini Grouvelle, 1899 , nec Anthystrix martini sensu KIREJTSHUK & EASTON (1988)
Tarchonanthogethes rotundiclava (Kirejtshuk & South Africa: Eastern Cape, KwaZulu-Natal Easton, 1988) comb. nov. (from Anthystrix )
Tarchonanthogethes singularis ( Grouvelle, 1919) South Africa or Zimbabwe (localization of type locality comb. nov. (from Meligethes ) uncertain)
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