Stachygethes Audisio & Cline, 2009
publication ID |
https://doi.org/10.5281/zenodo.5319334 |
persistent identifier |
https://treatment.plazi.org/id/03BE87CC-F62D-FFCE-BA6E-FD96FCE2FBA7 |
treatment provided by |
Felipe (2021-08-28 07:26:47, last updated 2021-08-29 12:01:59) |
scientific name |
Stachygethes Audisio & Cline |
status |
gen. nov. |
20. Stachygethes Audisio & Cline , gen. nov.
( Figs. 20 a–k)
Type species. Nitidula ruficornis Marsham, 1802: 131 (= Meligethes ruficornis ( Marsham, 1802) (by present designation) [= Stachygethes ruficornis ( Marsham, 1802) comb. nov.].
Generic description and diagnosis. Inclusive species vary greatly in size (1.5–3.8 mm length), and share the following combination of characters.
Body color and pubescence: pubescence silvery-whitish, variably developed, recumbent, never obscuring the blackish or dark brown and usually shining dorsal body surface; pronotal and elytral sides narrowly flattened, typically the same color as disc. 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 long, usually distally bifid or trifid microsetae, microsetae uniformly distributed on middle region anterior to scutellum ( Fig. 20e).
Dorsal habitus: body more or less convex, variably shaped, usually moderately slender and oval ( Figs. 20a, b); dorsal punctures on discal portion of pronotum as large as or larger than eye facets, usually deeply impressed and densely distributed; anterior margin of clypeus truncate, and distinctly narrowly bordered ( Fig. 20c), without small, faintly distinct, medial bulge; circum-ocular furrows (occipital sulci) on dorsal side of head narrow, moderately impressed, and anteriorly developed ( Fig. 20c); eyes large and usually moderately projecting laterally ( Figs. 20a, b, c); pronotum with obtusely distinct or almost completely rounded posterior angles, never directed posteriorly ( Figs. 20a, b); scutellum regularly punctured on posterior half of exposed portion ( Fig. 20e); elytra never transversely strigose, punctation simple, occasionally with faint traces of orange peel-like rugosity; elytral humeral angle moderately distinct, not protruding laterally ( Figs. 20a, b); elytral humeral striae faint; elytral pre-sutural striae distinct, originating posteriorly to scutellar vertex, terminating close to elytral apex, delimiting on each elytron a flat and narrow sutural border, narrower than proximal portion of 3 rd antennomere; elytral apices truncately rounded in both sexes ( Fig. 20a); pygidium partially exposed, moderately convex, apically rounded in both sexes ( Figs. 20a, b).
Ventral habitus: antennal furrows markedly delimited, nearly parallel-sided; mentum subpentagonal ( Fig. 20d); prosternal antennal furrows on anterior margin of prosternum strongly raised and relatively long ( Fig. 20d); prosternal process usually relatively narrow, subapical dilated portion 2.3–2.8× as wide as maximum width of 1 st antennomere, apex usually bluntly acuminate ( Fig. 20g); lateral borders of prosternal process delimiting shallowly impressed but distinct furrows, distally terminating over predistal lateral expansions near posterior margin ( Fig. 20g); posterior margin of mesoventrite simple, never medially incised ( Fig. 20g); male impressions on metaventrite scarcely developed; first two visible abdominal ventrites simple in both sexes, without tufts of setae; caudal marginal lines of metacoxal cavities simple, parallel and contiguous to posterior margin of metacoxal cavities, comprising moderately deep arched impression of outer ‘axillary’ line ( Fig. 20f); ‘axillary’ space on first abdominal ventrite reduced, ‘axillary’ angle nearly right angled ( Fig. 20f); relatively large, long, and deeply impressed arched impressions on basal portion of last visible abdominal ventrite, frequently partially covered by distal portion of penultimate visible abdominal ventrite ( Fig. 20h).
Appendages: male 1 st antennomere 0.7–0.9× as long as width of protibiae excluding distal teeth ( Figs. 20a, b, d); 3 rd antennomere in both sexes 1.6–1.8× as long as wide, 0.8–0.9× as long as but distinctly thinner than 2 nd antennomere ( Fig. 20d); 4 th and 5 th antennomeres subequal in both sexes, short, nearly as long as wide; antennal club compact, small, simple, comprising last 3 antennomeres in both sexes (8 th antennomere scarcely widened, 0.4–0.5× as wide as 9 th antennomere) ( Figs. 20a, b, d), narrower than width of protibiae, sexual dimorphism absent; labial palpi relatively short in both sexes ( Fig. 20d), terminal segment ~1.7× as long as wide; maxillary palpi moderately long and slender in both sexes ( Fig. 20d), terminal segment 2.0–2.1× as long as wide; mandible mid-sized ( Fig. 20d), apex moderately acuminate, no sexual dimorphism; tarsal claws simple, never toothed at base; tarsi of normal size and shape, 0.6–0.7× as long as corresponding tibiae ( Figs. 20a, b); protibiae with a series of variable, even or uneven, large or small, sharp or blunt teeth on lateral margin ( Figs. 20a, b, g; Figs. 129 a, 131 g –q, s–u in AUDISIO 1993b); lateral margin of meso- and metatibiae bearing a single usually even row of large and robust pegs ( Fig. 20k), without U-shaped sinuosity at distal third; meso- and metatibiae of variable width, usually moderately slender and narrow ( Figs. 20a, b), never subtrapezoidal or axe-shaped; sexual dimorphism rarely expressed in male metatibiae; tarsal plates of prolegs distinctly wider in males; posterior margin of metafemora simple in both sexes, without tubercles or projections.
Male genitalia: processes along inner side of parameres absent (Figs. 139 q–r, 142 a–o, 143 in AUDISIO 1993b), with variably incised distal margin, without deep median longitudinal desclerotization from proximal portion of tegmen extending to medial distal V-shaped excision; median lobe of aedeagus variable, without lateral emargination, narrowed and subtruncate or acuminate distally, without distal marked excision or emargination.
Female genitalia (ovipositor): variably shaped, usually large; styli short to long, simple, cylindrical, inserted in variable position prior to apex of contiguous or divergent gonostyloids (Figs. 158 b–e, m, 159 a–l in AUDISIO 1993b); each gonostyloid moderately sclerotized and frequently more darkly pigmented distally, with a simple, never indentate outer portion of basicoxites, and a single, narrow, lightly pigmented and sclerotized arcuate area along outer subdistal portion of gonostyloids. ‘Central point’ of ovipositor usually centrally located, without proximad directed spicule.
Etymology. The generic name is derived from Stachys L. ( Lamiaceae ), to emphasize the strict larval relationships of several species with members of this widespread plant genus and allied genera, and from ‘- gethes ’, to emphasize its phylogenetic relationship with Meligethes . Gender masculine.
Biology. Biology of inclusive species is incompletely known, but homogeneous within the genus. Members of Stachygethes gen. nov. are all associated as larvae with flowers of Lamiaceae (= Labiatae ), in particular Salvia L., Stachys L., Ballota L., Marrubium L., and allied genera in Palaearctic areas ( EASTON 1964a; AUDISIO 1993b, and unpublished data).
Phylogenetic position. Available morphological datasets provide evidence of a possible clade including Stachygethes gen. nov., Lamiogethes gen. nov., and potentially Rubiogethes gen. nov., Paleogethes gen. nov., Jelinekigethes gen. nov., and Astylogethes . However, phylogenetic relationships between these taxa remain unclear, and are only partially supported with molecular data ( TRIZZINO et al. 2009).
Taxonomy and geographic distribution. Stachygethes gen. nov. includes 17 described species, as well as some identified but undescribed species. The genus is mainly distributed in Europe, Anatolia, and Middle Asia ( KIREJTSHUK 1992b; AUDISIO 1993b, and unpublished data; JELÍNEK & AUDISIO 2007). Inclusive species are attributed to two formerly recognized species-groups, i.e. the ‘ Meligethes ruficornis ’, and ‘ M. assimilis ’ species-groups.
Stachygethes assimilis ( Sturm, 1845) comb. nov. Europe
Stachygethes dilutipes (Easton, 1957) comb. nov. Middle Asia
Stachygethes khnzoriani (Kirejtshuk, 1979) comb. nov. Turkey, Caucasus
Stachygethes lederi ( Reitter, 1871) comb. nov. N Africa, S Iberian Peninsula
Stachygethes maroccanus ( Easton, 1956) comb. nov. Morocco
Stachygethes nanus ( Erichson, 1845) comb. nov. Europe, N Africa, Near East, W Middle Asia Stachygethes nigerrimus ( Rosenhauer, 1856) comb. nov. N Africa, SW Europe
Stachygethes rotroui ( Easton, 1952) comb. nov. N Africa
Stachygethes ruficornis ( Marsham, 1802) comb. nov. Europe, N Africa, Near East, W Middle Asia Stachygethes saxatilis (Audisio, 1988) comb. nov. E Turkey, W Iran
Stachygethes scholzi ( Easton, 1960) comb. nov. S Italy, Sicily, W Balkans
Stachygethes strejceki (Jelínek, 1982) comb. nov. Uzbekistan
Stachygethes syriacus (C. N. F. Brisout Middle East de Barneville, 1872) comb. nov.
Stachygethes turcicus (Jelínek, 1982) comb. nov. Turkey
Stachygethes variolosus (Easton, 1964) comb. nov. S Europe, Caucasus, Turkey
Stachygethes villosus (C. N. F. Brisout Europe, N Africa de Barneville, 1863) comb. nov.
Stachygethes zarudnyi ( Kirejtshuk, 1984) comb. nov. SE Turkey, NW Iran
AUDISIO P. 1993 b: Coleoptera Nitidulidae - Kateretidae. Fauna d'Italia. Vol. 32. Calderini Edizione, Bologna, xvi + 971 pp.
BRISOUT DE BARNEVILLE C. N. F. 1863: [new taxa]. In: GRENIER A. (ed.): Catalogue des Coleopteres de France, et materiaux pour servir a la faune des Coleopteres Francais. A. Grenier, Paris, iv + 9 - 79 + 1 - 135 pp.
EASTON A. M. 1952: A review of the Meligethes (Col., Nitidulidae) associated with the Labiate Marrubium vulgare L., including the description of a new species. Bulletin de la Societe des Sciences Naturelles du Maroc 32: 181 - 192.
EASTON A. M. 1956: The Meligethes of North Africa (Coleoptera, Nitidulidae). Memoires de la Societe des Sciences Naturelles et Physiques du Maroc, Serie Zoologie 2 (1955): 7 - 70.
EASTON A. M. 1960: The Meligethes of East Africa (Coleoptera: Nitidulidae). Transactions of the Royal Entomological Society of London 112: 263 - 318.
EASTON A. M. 1964 a: Meligethes rosenhaueri Reitter, M. assimilis Sturm and related species (Coleoptera: Nitidulidae). Proceedings of the Royal Entomological Society of London (B) 33: 1 - 6.
ERICHSON W. F. 1845 - 1848: [I., II. Lieferungen]. Pp. 1 - 320. In: Naturgeschichte der Insecten Deutschlands. Erste Abtheilung. Coleoptera. Dritter Band. Nikolaische Buchhandlung, Berlin, iv + [ii] + 968 pp. [issued in parts: pp. 1 - 320: 1845; pp. 321 - 480: 1846; pp. 481 - 800: 1847; pp. 801 - 968: 1848].
JELINEK J. & AUDISIO P. 2007: Family Nitidulidae. Pp. 459 - 491. In: LOBL I. & SMETANA A. (eds): Catalogue of Palaearctic Coleoptera. Vol. 4: Elateroidea - Derodontoidea - Bostrichoidea - Lymexyloidea - Cleroidea - Cucujoidea. Apollo Books, Stenstrup, 935 pp.
KIREJTSHUK A. G. 1984: New taxa of Nitidulidae (Coleoptera) from the Indo-Malayan fauna. Annales Historico- Naturales Musei Nationalis Hungarici 76: 169 - 195.
KIREJTSHUK A. G. 1992 b: 59, 61. Sem. Nitidulidae - Blestyanki. Pp. 114 - 209. In: LER P. A. (ed.): Opredelitel'nasekomykh Dal'nego Vostoka SSSR v shesti tomakh. Tom III. Zhestkokrylye, ili zhuki. [Key to the insects of the Far East of the USSR in six volumes. Vol. 3, Coleoptera]. Nauka, Sankt-Petersburg, 704 pp (in Russian).
MARSHAM T. 1802: Coleoptera Britannica, sistens Insecta Britanniae indigena, secundum methodum linnaeanam disposita. Tomus I. Coleoptera. Wilks et Taylor, Londini, xxxi + 547 + [1] pp.
REITTER E. 1871: Revision der europaischen Meligethes-Arten. Verhandlungen des Naturforschenden Vereines in Brunn 9: 39 - 169.
ROSENHAUER W. G. 1856: Die Thiere Andalusiens nach dem Resultate einer Reise zusammengestellt, nebst den Beschreibungen von 249 neuen oder bis jetz noch unbeschriebenen Gattungen und Arten. T. Blaesing Verlag, Erlangen, 429 pp.
STURM J. 1845: Deutschlands Fauna in Abbildungen nach der Natur mit Beschreibungen. V. Abtheilung. Die Insecten. Zweites Bandchen. Kafer. Nurnberg, 114 pp + pls. ccciv - cccix.
TRIZZINO M., AUDISIO P., ANTONINI G., DE BIASE A. & MANCINI E. 2009: Comparative analysis of sequences and secondary structures of the rRNA internal transcribed spacer 2 (ITS 2) in pollen-beetles of the subfamily Meligethinae (Coleoptera, Nitidulidae): potential use of slippage-derived sequences in molecular systematics. Molecular Phylogenetics and Evolution 51: 215 - 226.
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