Neolariopsis Audisio & Cline, 2009

Audisio, Paolo, Cline, Andrew Richard, Biase, Alessio De, Antonini, Gloria, Mancini, Emiliano, Trizzino, Marco, Costantini, Lorenzo, Strika, Sirio, Lamanna, Francesco & Cerretti, Pierfilippo, 2009, Preliminary re-examination of genus-level taxonomy of the pollen beetle subfamily Meligethinae (Coleoptera: Nitidulidae), Acta Entomologica Musei Nationalis Pragae 49 (2), pp. 341-504 : 360-363

publication ID

https://doi.org/ 10.5281/zenodo.5319334

DOI

https://doi.org/10.5281/zenodo.10542344

persistent identifier

https://treatment.plazi.org/id/03BE87CC-F679-FF92-BA64-FCBBFEA2FC2C

treatment provided by

Felipe

scientific name

Neolariopsis Audisio & Cline
status

gen. nov.

5. Neolariopsis Audisio & Cline , gen. nov.

( Figs. 5 a–h View Fig )

Type species. Meligethes cercoides Reitter, 1872: 248 (by present designation) [= Neolariopsis cercoides (Reitter, 1872) comb. nov.].

Generic description and diagnosis. Inclusive species vary moderately in size (1.6–2.2 mm length), and share the following combination of characters.

Body color and pubescence: pubescence golden to silvery-whitish, variable, short and fine, recumbent, or moderately long, suberect, never obscuring the variably colored dorsal body surface (yellowish, reddish, brown, blackish, frequently with metallic bronze iridescence, or blackish with orange spots on elytra: Figs. 5a, b View Fig ); pronotal and elytral sides narrowly flattened, typically same color as disc. Lateral margin of pronutum and elytra typically with series of distinct setae, each seta 0.7–0.8× as long as those on elytral disc; posterior margin of pronotum comprising moderately long, usually distally trifid or tetrafid microsetae, microsetae uniformly distributed on middle region anterior to scutellum (as in Fig. 3e View Fig ).

Dorsal habitus: body more or less convex, variably shaped, usually moderately slender and oval ( Figs. 5a, b View Fig ); 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 moderately to strongly arcuately emarginate, simple, i.e. without small distinct bulge medially, distinctly and widely bordered ( Fig. 5c View Fig ), circum-ocular furrows (occipital sulci) on dorsal side of head almost complete, narrow, moderately to deeply impressed ( Fig. 5c View Fig ); eyes large and usually moderately projected laterally ( Figs. 5a, c View Fig ); pronotum with faintly distinct posterior angles, rounded to obtuse and never directed posteriorly ( Figs. 5a, b View Fig ); scutellum regularly punctured in most of exposed portion; elytra usually with simple punctation, never completely transversely strigose, occasionally with faint traces of orange peel-like rugosity, or with faint traces of uneven rugosity (e.g. N. odiosus ); elytral humeral angle moderately distinct, not protruding laterally ( Figs. 5a, b View Fig ); elytral humeral striae absent; elytral pre-sutural striae visible, originating at scutellar vertex, terminating at elytral apex, and delimiting on each elytron a faintly distinct, flat, unraised sutural border, border widest at posterior third and slightly narrower than proximal width of 3 rd antennomere; elytral apices truncately rounded in both sexes ( Fig. 5a View Fig ); pygidium partially exposed, moderately convex, rounded apically in both sexes ( Figs. 5a, g View Fig ).

Ventral habitus: antennal furrows markedly delimited, nearly parallel-sided, slightly convergent posteriorly, mentum subpentagonal ( Fig. 5d View Fig ); prosternal antennal furrows moderately raised and short at anterior margin of prosternum ( Fig. 5d View Fig ); prosternal process typically narrow, subapical dilated portion 1.6–1.8× as wide as maximum width of 1 st antennomere, and usually apically bluntly acuminate ( Fig. 5f View Fig ); lateral borders of prosternal process delimiting shallowly impressed but distinct furrows, distally terminating over predistal lateral expansions ( Fig. 5f View Fig ); posterior margin of mesoventrite simple, never incised medially ( Fig. 5f View Fig ); 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, without arched impression of outer ‘axillary’ line (as in Fig. 4k View Fig ); ‘axillary’ space on first abdominal ventrite moderately developed, ‘axillary’ angle widely obtuse (as in Fig. 4k View Fig ); relatively large but short and shallowly impressed arched impressions on basal portion of last visible abdominal ventrite, frequently partially covered by distal portion of penultimate visible abdominal ventrite ( Fig. 5g View Fig ).

Appendages: male 1 st antennomere 0.8–1.0× as long as width of protibiae excluding distal teeth ( Figs. 5a, b, d View Fig ); 3 rd antennomere in both sexes 2.0–2.1× as long as wide, 0.9–1.0× as long but distinctly thinner than 2 nd antennomere ( Fig. 5d View Fig ); 4 th and 5 th antennomeres in both sexes subequal, 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. 5a, b, d View Fig ), much narrower than width of protibiae, sexual dimorphism absent; labial palpi relatively short in both sexes ( Fig. 5d View Fig ), terminal segment 1.7–1.8× as long as wide; maxillary palpi moderately long and slender in both sexes ( Fig. 5d View Fig ), terminal segment 2.1–2.2× as long as wide; mandible mid-sized ( Fig. 5c View Fig ), apex moderately acuminate, no sexual dimorphism present; tarsal claws simple, never toothed at base ( Fig. 5e View Fig ); tarsi of normal size and shape, 0.5–0.7× as long as corresponding tibiae ( Figs. 5a, b, e View Fig ); protibiae with a series of usually small, even, moderately sharp teeth on lateral margin ( Figs. 5a, b View Fig ; Figs. 81–85 in KIREJTSHUK & AUDISIO 1995); meso- and metatibiae on lateral margin bearing a single and usually even row of large and robust pegs ( Fig. 5e View Fig ), without U-shaped sinuosity at distal third; meso- and metatibiae of variable width, usually moderately slender and narrow ( Figs. 5a, b View Fig ), never subtrapezoidal or axe-shaped; no sexual dimorphism in tibial shape; tarsal plates of prolegs sligthly 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. 29–38 View Fig View Fig View Fig View Fig View Fig View Fig View Fig View Fig View Fig and 45–46 in KIREJTSHUK & AUDISIO 1995), usually comprising moderately deep and narrow excision along distal margin, and always without deep median longitudinal desclerotization from proximal portion of tegmen extending to medial distal V-shaped excision; median lobe of aedeagus variable, without emargination laterally, rounded, subtruncate to acuminate distally, without distal marked excision or emargination.

Female genitalia (ovipositor): small; styli moderately long and distinct, simple, cylindrical, usually distinctly pigmented, inserted close to apex of contiguous gonostyloids; each gonostyloid moderately sclerotized and more heavily pigmented distally, with a simple, never indentate outer portion of basicoxites (Figs. 55–59 in KIREJTSHUK & AUDISIO 1995), and a single, narrow, moderately pigmented and sclerotized arcuate area along outer subdistal portion of gonostyloids. ‘Central point’ of ovipositor usually centrally located, with or without proximad directed spicule.

Etymology. The generic name is derived from a combination of the Greek ‘ νΈΟΣ ’ (= new), and Lariopsis , emphasizing its relatively more derived position within the Lariopsis complex of genera. Gender masculine.

Biology. All species are likely to be strictly associated for larval development with inflorescences and flowers of Mesembryanthemaceae s. l. (including Aizoaceae ), particularly with Ruschia Schwant. and allied genera, and with Tetragonia L. ( KIREJTSHUK & AUDISIO 1995, and unpublished data).

Phylogenetic position. See discussion above regarding the phylogenetic placement of Odontholariopsis gen. nov.

Taxonomy and geographic distribution. Neolariopsis gen. nov. includes six described species distributed in Southern Africa ( KIREJTSHUK & AUDISIO 1995), which are divided into two species groups (i.e. the cercoides , and odiosus species-groups). A few additional species still awaiting description are known to the authors from the same geographical area.

Neolariopsis cercoides (Reitter, 1872) comb. nov. South Africa: W Cape

Neolariopsis odiosus (Reitter, 1872) comb. nov. South Africa: W Cape

Neolariopsis pulchellus (Reitter, 1872) comb. nov. South Africa: Free State, Gauteng, KwaZulu- Natal; Lesotho;? Angola

Neolariopsis serrula ( Kirejtshuk & Easton, 1988) comb. nov. Lesotho

Neolariopsis serruloides ( Kirejtshuk & Audisio, 1995) comb. nov. South Africa: W Cape

Neolariopsis thalycroides ( Kirejtshuk & Audisio, 1995) South Africa: W Cape comb. nov.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Coleoptera

Family

Nitidulidae

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