Bondariella torresi Bondar, 1942
publication ID |
https://doi.org/ 10.11646/zootaxa.4018.2.3 |
publication LSID |
lsid:zoobank.org:pub:065A82FD-3F0A-43DF-AEF4-168BDFBF866F |
DOI |
https://doi.org/10.5281/zenodo.6120000 |
persistent identifier |
https://treatment.plazi.org/id/03F08799-7477-FFE0-7087-EB06E6C3C18B |
treatment provided by |
Plazi |
scientific name |
Bondariella torresi Bondar, 1942 |
status |
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Bondariella torresi Bondar, 1942 View in CoL
( Figs. 1 View FIGURE 1 B, 3G, 5)
Bondariella torresi Bondar, 1942: 22 View in CoL ; Bondar 1943: 370 (natural history); Vaurie 1953: 37 (lectotype designation); Wibmer & O’Brien 1986: 316 (catalogue).
Male ( Figs. 1 View FIGURE 1 B, 3G, 5). Length of pronotum + elytra: 2.3–2.6mm (N=10). Integument ( Fig. 1 View FIGURE 1 B) evenly light reddish brown throughout, generally darker on punctures of elytral striae; covered by large yellowish spatulate scales. Rostrum ( Fig. 1 View FIGURE 1 B) 0.9 times as long as pronotum, curved in lateral view. Antennae: antennal insertion premedian (0.4); scape 1.9 times as long as article I of funicle. Pronotum 1.2–1.3 times wider than long; disc with large and closely spaced punctures (distant by 0.3 times their own diameter); scales subequal in length throughout; median line slightly convex; collar slightly evident, marked by darker strip of punctures. Interprocoxal distance slightly larger (1.2–1.3 times) than procoxal diameter. Femora lacking comb of setae. Metatibiae strongly clavate to apex, sinuous on dorsal face and with a comb of long setae on distal ½. Elytra 1.2–1.4 times longer than wide; 2.0–2.3 times as long as pronotum; sutural interval with two rows of scales; remaining intervals with 2–3 rows of scales on base, becoming variously two rows toward apex. Abdominal tergites ( Figs. 3 View FIGURE 3 G, 5A): laterotergites subdivided into three smaller sclerites; median fissure complete, reaching distal margin of tergite IV; tergite IV with lateral and median spiculate patches on median sclerites; tergite VII with two rows of plectra, each with seven distantly spaced plectra. Ventrites ( Fig. 5 View FIGURE 5 B): I–II combined 2.0–2.3 times as long as III–IV combined; ventrite I 1.2–1.4 times as long as ventrite II; ventrite V transversally oblong, 3.4–3.6 times wider than long, flat, distal margin rounded, lacking tufts of scales. Sternum VIII ( Fig. 5 View FIGURE 5 C): each sclerite trapezoidal, with six posteroventral setae. Spiculum gastrale ( Fig. 5 View FIGURE 5 D) 2.0 times as long as median lobe; stylus curved, relatively wide; furcal arms sclerotized, elongate, narrowed, not clavate, symmetrical. Tegmen ( Fig. 5 View FIGURE 5 E) sclerotized, 2.1 times as long as median lobe; dorsal parameroid lobes free (not connected medially on base), each parameroid lobe 0.6 times as long as median lobe, clothed with long setae on distal 1/2; ventral tegminal apodeme 0.7 times as long as median lobe, widened, short and straight to apex. Aedeagus ( Fig. 5 View FIGURE 5 F): median lobe short and wide, 2.0 times longer than wide; apex truncate; lateral margins narrowed; sides sinuous; endophallus membranous, clothed with sparse spinules on distal ½ (larger medially), with an anterior pair of membranous bags bearing numerous denser large spinules; ostium evident, distal; lacking orificial plates. Apodemes of aedeagus 1.5 times as long as median lobe, not sclerotized on basal 1/3.
Female ( Fig. 1 View FIGURE 1 B). Length of pronotum + elytra: 2.4–2.6mm (N=5). Differs from male by generic characters of the rostrum, scrobe, antennal scape, interocular distance and ventrite II (cited above). In addition, by rostrum ( Fig. 1 View FIGURE 1 B) strongly curved; scrobe 0.2 times as long as rostrum; antennal insertion basal (0.1 times); scape shorter than article I of funicle (0.7 times); pronotum lacking median line. Body part ratios. Length rostrum/length pronotum: 0.9 times; pronotum width/length: 1.3 times; elytron length/width: 1.3–1.4 times; length elytron/length pronotum: 2.0–2.2 times; interprocoxal distance/procoxal diameter: 1.2 times; length ventrite I/length ventrite II: 1.2–1.3 times; length ventrites I+II/length ventrites III+IV: 2.4–2.6 times; ventrite V width/length: 3.3–3.5 times.
Etymology. Named by Bondar (1942) in honour of his great friend Antonio Margarinos Torres.
Remarks. Bondariella torresi ( Fig. 1 View FIGURE 1 B), Bondariella rudicula sp. nov. ( Fig. 2 View FIGURE 2 B) and Bondariella crenata sp. nov. ( Fig. 2 View FIGURE 2 C) are similar by having integument evenly light reddish brown throughout. But Bondariella torresi is easily distinguished from Bondariella rudicula sp. nov. and Bondariella crenata sp. nov. by a number of characters: sutural interval of elytra with two rows of scales; remaining elytral intervals with 2–3 rows of scales on base, becoming variously two rows toward apex; rostrum curved (males), strongly curved and long (0.9 times as long as pronotum, females) ( Fig. 1 View FIGURE 1 B); interprocoxal distance larger (1.2–1.3 times) than procoxal diameter; metatibae bearing a comb of long setae on distal ½ (male); abdominal tergites ( Figs. 3 View FIGURE 3 G, 5A) with median fissure complete (reaching distal margin of tergite IV); ventrite V ( Fig. 5 View FIGURE 5 B) transversally oblong (3.3–3.6 times wider than long); sternum VIII ( Fig. 5 View FIGURE 5 C) trapezoidal bearing six posteroventral setae; tegmen ( Fig. 5 View FIGURE 5 E) with dorsal parameroid lobes free (not connected medially on base) and; endophallus ( Fig. 5 View FIGURE 5 F) membranous, with a pair of bags of spinules. On the other hand, Bondariella rudicula sp. nov. and Bondariella crenata sp. nov. have only one row of scales on sutural interval; remaining elytral intervals with 1–2 rows at base, becoming variously only one row toward apex; rostrum almost straight (males), straight and short (0.5–0.6 times as long as pronotum, females) ( Figs. 2 View FIGURE 2 B–C); interprocoxal distance slightly shorter (0.9 times) than procoxal diameter; metatibae lacking comb of setae; abdominal tergites ( Fig. 3 View FIGURE 3 F) with median fissure incomplete (not reaching distal margin of tergite IV); ventrite V ( Figs. 8 View FIGURE 8 B, 9B) trapezoidal (2.4–2.6 times wider than long); sternum VIII ( Figs. 8 View FIGURE 8 C, 9C) subquadrate and glabrous; tegmen ( Figs. 8 View FIGURE 8 E, 9E) with dorsal parameroid lobes connected medially on base; endophallus ( Figs. 8 View FIGURE 8 F, 9F) sclerotized, lacking membranous bags. Finally, B. torresi is distributed in Caatinga biome and has only been collected from Syagrus vagans while Bondariella rudicula sp. nov. and Bondariella crenata sp. nov. are distributed in Amazon biome and have only been collected from Euterpe species. The remaining species of Bondariella have been collected from different species of Syagrus .
Natural history. Bondariella torresi is recorded from the Caatinga biome, from Lajedo Alto and Morro do Chapéu, both localities in Bahia, Brazil. Adults and larvae of B. torresi were collected from Santa Luzia, Lajedo Alto on male flowers of Syagrus vagans , locally known as “ariri” (Bondar 1942, 1943, cited as Cocos vagans Bondar ). In the municipality of Morro do Chapéu, adults were collected on an unidentified palm. Larvae feed and complete their life cycle between petals of male flowers from open inflorescences of S. vagans (Bondar 1942, 1943). Bondar was able to rear larvae of B. torresi in the laboratory, but larvae and pupae not yet been described. Currently, Lajedo Alto (ex Lagedo Alto) is district of the municipality of Iaçu, which was dismembered from the municipality of Santa Teresinha (ex Santa Terezinha) (IBGE 2011). As spelled in the labels from type material we did not find the locality of Santa Tereza, so we believe that it could be the municipality of Santa Teresinha (ex Santa Terezinha) mispelled as Santa Tereza. To corroborate this interpretation, in the same paper, Bondar (1942) spelled Santa Teresinha or Santa Terezinha in labels of other two species of weevils collected on flowers of S. vagans . In additional collections besides the type series, Bondariella torresi has only been recorded on flowers of S. vagans (for details see natural history of Bondariella ).
Material examined. Lectotype male deposited in AMNH: “Lagedo [Lajedo] Alto,\ S. [Santa] Luzia,\ Bahia, Brazil [label 1], ♂ [label 2], Gregorio Bondar\ Collection\ David Rockefeller\ Donor [label 3], Lectotype \ Bondariella \ torresi \ Bondar\ P. Vaurie [label 4–rectangular, pink, print]”. Paralectotypes: “Estado da Bahia\ Brazil \ G. Bondar leg. [label 1], Lagedo [Lajedo] Alto\ Santa Luzia, Bahia\ Brazil \ Cocos vagans [label 2], Gregorio Bondar\ Collection\ David Rockefeller\ Donor [label 3]” ( AMNH: 7♂, 13♀); “Cotipo [label 1– rectangular, red, print], 1942\ Bahia\ S. [Santa] Tereza\ Bondar [label 2], Bondariella \ torresi Bond., 1942 \ cotipo\ H. Reichardt det. 1962 [label 3]” ( MZUSP: 4♂ (1 dissected), 2♀). Not Paralectotypes: “Morro do Chapéu, BA [Bahia]\ 28.x.1987 \ M. T. Rodrigues\ Col. [collected], em palmeira. [label 1], Bondariella \ torresi [label 2]” ( MZUSP: 2♂, 1♀), same date but, “ Bondariella \ torresi \ Bondar, 1942\ S. A. Vanin det. 1987 [as label 3]” ( MZUSP: 2♂, 1♀), same date but, “ Baridinae –\ Tribo Madarini \ Bondariella torresi [as label 2]” ( MZUSP: 2 ♂, 1 ♀).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Bondariella torresi Bondar, 1942
Valente, Roberta De Melo & Júnior, Mariano Brandão Cordeiro 2015 |
Wibmer 1986: 316 |
Vaurie 1953: 37 |
Bondar 1943: 370 |