Research Article
Print
Research Article
Systematics of the seed beetle genus Decellebruchus Borowiec, 1987 (Coleoptera, Bruchidae)
expand article infoJesús Romero Nápoles
‡ Instituto de Fitosanidad, Colegio de Postgraduados, Estado de México, Mexico
Open Access

Abstract

Keys to species, descriptions, synonymy, host plants, and geographical distributions are presented for the three species in the genus Decellebruchus (Borowiec 1987); of those, D. walker (Pic 1912) was the only species included at the time of the genus denomination, D. atrolineatus (Pic 1921) is transferred to this genus, and D. lunae is described as a new species. The shortest and most parsimonious phylogenetic tree for genera with pectinate antennae had a length of 33, consistency index 87, and retention index 81.

Keywords

Seed beetles, Decellebruchus , Bruchidae , cladistics

Introduction

The monotypic genus Decellebruchus was erected by Borowiec in 1987 with the type species Decellebruchus walkeri (Pic 1912). This species has a complicated history, starting with Bruchus figuratus that was described by Walker (1859); however this was a homonym and then Pic (1912) proposed the replacement name of Bruchus walkeri. Later Decelle (1975b) transferred it to Bruchidius, but because the unusual pectinate antennae of the species in the genus Bruchidius, Borowiec (1987) erected the monotypic genus Decellebruchus for it. Another species that has been included unofficially in the latter genus is Bruchus atrolineatus Pic, 1921; however B. atrolineatus has also suffered a series of generic changes through time. Finally the third species included in the genus is the new species D. lunae. In order to clarify the genus it is reviewed and a hypothesis of its phylogeny is proposed.

Material and methods

Specimens. Preparation of genitalia for study followed the techniques and nomenclature described by Kingsolver (1970) and modified by Romero and Johnson (1999). For specimens the following collections were consulted: Colección Entomológica del Colegio de Postgraduados, Montecillo, Estado de México, México (CEAM), Florida State Collection of Arthropods, Gainesville, Fl, USA (FSCA), Musee Zoologique de l’Universite de Lund, Lund University, Sweden (MZLU); South African National Collection of Insects, Queenswood, South Africa (SANC).

Cladistics. External morphological characters and internal characters, these latter only from male genitalia (Table 1) were used. Host plants and distribution were also considered. Taxa included in the analysis were only those bruchids with pectinate antennae (excluding the genera Caryedes and Gibbobruchus because they have only few species with pectinate antennae) and all species in the genus Decellebruchus. Pachymerus, a less derived genus was used as the outgroup. The data matrix is presented in Table 2. The program Hennig86 (Farris 1988) was used to generate the cladogram, although a comparative tree was obtained with Mesquite, version 3.04 (Maddison and Maddison 2015) using the same data matrix.

Table 1.

Characters used for the cladistic analysis for Bruchidae with pectinate antennae.

External morphology
0. Body length 8–16 mm: 0; 1.5–5.4 mm: 1
1. Eye sinus Shallow: 0; deep: 1
2. Male antenna shape Not pectinate: 0; pectinate 1
3. Last antennal segment About half as long as hind tibia: 0; as long as or longer than hind tibia: 1
4. Carina media on frons With carina: 0; without carina: 1
5.Pronotal carina Complete: 0; no complete:1
6. Pronotum shape Not conical, without distinctly concave sides: 0; conical with distinctly concave sides: 1
7. Pronotal disc Without gibbosites: 0; with gibbosites: 1
8. Scutellum shape Subsquare: 0; elongate: 1
9. Metepisternal sulcus With sulcus:0; without sulcus: 1
10. Tenth elytral stria Extending nearly to apex of elytron: 0; extending to half of elytron: 1
11. Elytral basal tubercles Without tubercles: 0; with tubercles: 1
12. Pygidium articulation Pygidium and penultimate tergum partially fused and no covered by elytra 1; Penultimate tergum no fused to pygidium and covered by elytra 2
13. Hind femur Without carinae: 0; with one carina or obsolete carinae 1; bicarinate: 2
14. Spines on hind femur With 10-14 spines: 0; with 1 to 3 spines: 1; without spines: 2
15. Hind tibia carinae With complete set of carinae: 0; incomplete set of carinae: 1
16. Tuft of white setae on fore coxa Without tuft of white setae: 0; with tuft of white setae: 1
17. Male pygidium Reclinate 0; vertical 1
Internal morphology
18. Lateral lobes of male genitalia Fused 0; divided 1
19. Ventral valve of male genitalia No arcuate: 0; deeply arcuate 1
20. Shape of apical portion of median lobe of male genitalia| No bulbous: 0; bulbous: 1
21. Basal strut of lateral lobes of male genitalia With an obsolete or small perpendicular keel: 0; with strong perpendicular keel 1
22. Armature of internal sac of male genitalia Only with spinules: 0; with spinules and small teeth 1
Ecological characters
23. Distribution Worldwide 0; New world 1; Old world: 2
24. Host plants Arecaceae: 0; Fabaceae: 1; Convolvulaceae: 2
Table 2.

Data matrix.

Taxa Character
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
1. Pachymerus 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0
2. Kytorhinus 1 1 1 1 0 1 0 0 1 1 0 0 1 1 2 1 0 1 0 0 0 0 0 0 1
3. Megacerus 1 1 1 1 1 1 0 0 0 1 1 0 0 1 1 0 0 1 0 0 0 0 0 1 2
4. Callosobruchus 1 1 1 1 1 1 0 1 0 1 0 1 0 2 1 0 0 1 1 0 0 0 0 2 1
5. Conicobruchus 1 1 1 1 1 1 1 0 0 1 0 0 0 1 1 1 0 0 1 0 0 0 0 2 1
6. Rhipibruchus 1 1 1 1 1 1 0 1 0 1 0 1 0 1 1 0 0 1 1 0 0 0 0 1 1
7. Pectinibruchus 1 1 1 1 1 1 0 1 1 1 0 0 0 1 1 1 0 1 1 0 0 0 0 1 1
8. D. atrolineatus 1 1 1 1 1 1 0 1 0 1 0 1 0 1 1 0 1 1 1 1 0 0 0 2 1
9. D. walkeri 1 1 1 1 1 1 0 1 0 1 0 1 0 1 1 0 1 1 1 1 1 0 1 2 1
10. D. lunae 1 1 1 1 1 1 0 1 0 1 0 1 0 1 1 0 1 1 1 1 0 1 1 2 1

Results and discussion

Key to genera of Bruchidae with pectinate antennae

1 Pygidium with one or two tergites exposed behind elytra; antenae in males pectinate or strongly serrate, in female serrate Kytorhinus Bridwell
Pygidium covered at base by elytra 2
2 Tenth elytral stria shortened, extending to middle of elytron; antennae in males pectinate, in female serrate Megacerus Fahraeus
Tenth elytral stria extending nearly to apex of elytron 3
3 Hind femur bicarinate, with spine on both internal and external ventral margins; antennae in males strongly serrate or pectinate, in female subserrate or serrate Callosobruchus Pic
Hind femur not bicarinate or carinae obsolete, or only ventral carina present 4
4 Pronotum conical with distinctly concave sides, antennae in males serrate or pectinate, in female subserrate Conicobruchus Decelle
Pronotum not conical, without distinctly concave sides 5
5 Last antennal segment as long as or longer than hind tibia 6
Last antennal segment about half as longer as hind tibia Decellebruchus Borowiec
6 Hind tibia carinate, mucro longer than lateral coronal denticle; scutellum subcuadrate Rhipibruchus Bridwell
Hind tibia with obsolete lateral carina, mucro absent; scutellum elongate Pectinibruchus Kingsolver

Key to species of Decellebruchus

1 Hind femur with only 1 subapical spine 2
Hind femur with 1 subapical spine followed by 2 smaller spines Decellebruchus walkeri (Pic)
2 Pygidium with basal spot of white pubescence; antennomere VII 1.76-2.0X wider that longer; hind femur with subapical acuminate spine about as long as width of tibial base Decellebruchus lunae Romero, sp. n.
Pygidium with two pubescent spots apically; antennomere VII 4.4-5.6X wider than longer; hind femur with small subapical acuminate spine about half as long as width of tibial base Decellebruchus atrolineatus (Pic)

Taxonomy

Decellebruchus Borowiec

Decellebruchus Borowiec, 1987: 149.

Description

Male. Vestiture: Moderately dense or dense, variegated; front coxa with a wide tuft of white setae. Body oval and stout. Head: Short, strongly constricted behind eyes, postocular lobe very short; eyes bulging, deeply emarginate; frons narrow, with sharp median carina; antennae pectinate from 4th or 5th segment. Prothorax: Pronotum subconical, without lateral carina; disc convex, slightly gibbous before scutellum and with shallow median channel; prosternal process narrow, triangular, acute. Meso- and metathorax: Scutellum square, bidentate apically; elytral striae regular; striae 4 and 5 abbreviated basally by tubercle. Legs: Metacoxa densely punctate; hind femur moderately swollen, ventral carinae obsolete. Internal ventral margin with small subapical spine, often followed by two smaller spines; hind tibia straight, enlarged, with complete or incomplete set of carinae, mucro longer than lateral coronal denticle. Abdomen: More or less telescoped, fifth sternite deeply emarginated; pygidium vertical. Genitalia: Internal sac of male genitalia lined with fine spines with or without sclerites; ventral valve deeply arcuate. Female. Similar to male, except antenna not pectinate, eyes less bulging, pygidium subvertical, last abdominal sternite not emarginated.

Decellebruchus atrolineatus (Pic, 1921), comb. n.

Bruchus atrolineatus Pic, 1921: 15, 1932: 36; Decelle 1951: 184, 1961: 8, 1975a: 21 (comb. n.).

Bruchidius atrolineatus: Prevett 1961: 636, 1967: 5, 1971: 247; Booker 1967: 2; Luca 1968a: 188, 1968b: 589; Decelle 1975a: 15; Southgate 1978: 219; Biemont et al. 1982: 2610; Hamon et al. 1982: 327; Pfaffenberger 1985: 3; Germain et al. 1987: 157; Monge et al. 1988: 297, 1989: 95; Huignard et al. 1989: 197; Pouzat and Nammour 1989: 319; Udayagiri and Wadhi 1989: 119; Lenga et al. 1990: 79; Glitho and Huignard 1990: 195; Pfaffenberger and Monge 1991: 309; Pichard et al. 1991: 185; Shimada and Ishihara 1991: 289; Credland 1992: 1; Ishihara and Shimada 1995: 127; Ofuya and Credland 1996: 323; Kingsolver 1988; Sanon et al. 2005; Löbl and Smetana 2010: 341.

Callosobruchus atrolineatus: Zacher 1952: 465; Shomar 1963: 178.

Bruchus semiflabellatus Pic, 1931; Bondar 1936: 37 (syn.); Kingsolver and Silva 1991: 413 (syn.); Udayagiri and Wadhi 1989: 119.

Acanthoscelides semiflabellatus: Blackwelder 1946: 761.

Callosobruchus semiflabellatus: Zacher 1952: 465.

Decellebruchus atrolineatus: Anton 1994: 100; Kergoat et al. 2005: 605 (without indicating clearly new combination).

Description

Male (Fig. 1a–b). Length (pronotum-elytra): 2.4–2.6 mm; width: 1.4–1.6 mm; maximum thoracic depth 1.5–1.7 mm. Color: Antennae with the first three segments yellowish, the rest dark or partially dark; head, prosternum, metasternum, base of meso-femur and meta-femora, and coxae dark; pronotum with two longitudinal dark bands, which may together form a dark spot; elyton variegate; pygidium with three pairs of dark spots, two apical, two median-lateral, and two basal; rest of body yellowish. Vestiture: Body with mixed yellowish and white pubescence; scutellum with whitish pubescence; fore coxa with a tuft of white setae; pygidium with yellowish and whitish pubescence forming a variegate pattern. Head: Short and broad, densely micropunctulate, frons with a strong median carina, distance between eyes 2.3.–3.3× as wide as eye width, eye cleft 0.60–0.71× its length by ocular sinus, posterior margin of eye protruding from adjacent surfaces, postocular lobe rounded and setose; distance from base of antennae to apex of labrum 0.39–0.55× as long as distance from upper limits of eyes to apex of labrum; antennomeres I–III filiform, IV subserrate, V–XI pectinate; antennomere II 2.8–3.8× as long as antennomere XI; antennomere VII 4.4–5.6× wider that long; antenna extending slightly beyond humerus. Prothorax: Subconical, without lateral carina; densely foveolate, disc convex, slightly gibbous before scutellum and with shallow median channel; prosternal process narrow, triangular, acute, half as long as procoxae. Meso- and metathorax: Scutellum square, bidentate apically; elytral striae regular, striae 4 and 5 abbreviated basally by tubercle, humeri raised. Legs: First protarsomere 2.0–3.0× as long as second, first mesotarsomere 1.8–2.3× as long as second, first metatarsomere 2.6–3.0× as long as second; metacoxa densely punctate; hind femur constricted basally and apically, expanded medially to about width of coxa; without external carina ventrally; internal ventral carina with small subapical acuminate spine about half as long as width of tibial base; hind tibia straight, enlarged, with only mesal and ventral carinae; tibial corona with 4 spinules, mucro 0.10–0.13× as long as first tarsomere; without sinus at base of spine; first hind tarsomere with ventrolateral glabrous longitudinal carina. Abdomen: Pygidium vertical (Fig. 2); last sternite emarginate. Genitalia: Median lobe moderately long, ventral valve triangular and deeply arcuate, internal sac with many small spines or needles, without large sclerites (Fig. 3a); lateral lobes elongate, expanded at apex, cleft about 0.53 their length; basal strut an obsolete perpendicular keel (Fig. 3b). Female (Fig. 4a–b). Length (pronotum-elytra) 2.4–2.8 mm, width: 1.5–1.7 mm, Maximum thoracic depth 1.6–1.8 mm. Similar to male except antennae serrate; distance between eyes 1.8.–2.0× as wide as eye width; pygidium subvertical; last sternite not emarginate.

Figure 1. 

Male habitus of Decellebruchus atrolineatus; a dorsal view b lateral view.

Figure 2. 

Male pygidium of Decellebruchus atrolineatus.

Figure 3. 

Male genitalia of Decellebruchus atrolineatus; a median lobe b lateral lobes.

Figure 4. 

Female habitus of Decellebruchus atrolineatus; a dorsal view b lateral view.

Material examined

NAMIBIA: Rundu, 28/V/2015, T. Chauke, 17°55’S 19°46’E, reared seed Glycine max (L.), intercepted at Pretoria SAAFQIS Plant Quarantine Station, South Africa, Sample Pta. 2811 (1 ex SANC). Caprivi region, 2002, intercepted at Pretoria SAAFQIS Plant Quarantine Station, South Africa (70 ex SANC). AFRICA: Intercepted at USA, 36/XII/2003, reared seed Phaseolus sp. (3 ex, FSCA); Intercepted at Atlanta, USA, 10/IX/2006, reared seed Phaseolus vulgaris L. (1 ex., FSCA). DEMOCRATIC REPUBLIC OF THE CONGO: N of Shaba Province, 28/III/1980, Whitecomb W.H., in cowpeas (1 ex., FSCA). NIGERIA: Intercepted at USA, 2/II/2004, Phaseolus sp. (7 ex., FSCA); Intercepted at USA, 3/II/2004, reared seed Phaseolus sp. (2 ex., CEAM). MEXICO: Ocolome, El Fuerte, Sinaloa, 21/I/2013, Lugo G.G.A., reared seed Vigna unguiculata (L.) WALP. (190 ex., CEAM).

Host plants

Dolichos lablab L., Glycine max (L.), Phaseolus vulgaris L. Vigna unguiculata (L.) Walp., Vigna unguiculata subsp. stenophylla (Harv.) Maréchal & Al., Vigna unguiculata subsp. unguiculata (L.)Walp. (Fabaceae). Zacher (1952) stated that Lablab niger Medik. and Medicago sativa L. are plant hosts of D. atrolineatus, however this information must be corroborated.

Distribution

Algeria, Angola, Brazil, Burkina Faso, Cameroon, Central African Republic, Democratic Republic of the Congo, Egypt, Ethiopia, Gambia, Ghana, Jamaica, Kenya, Liberia, Mali, Mexico, Mozambique, Namibia, Niger, Nigeria, South Africa, Saudi Arabia, Senegal, Sudan, Tanzania, Uganda, United Kingdom, Yemen, Zanzibar.

Discussion

Decellebruchus atrolineatus has high economic importance, because it is a pest mainly in species in the genus Vigna. It is frequently found together with Callosobruchus maculatus (F.). Large losses due to this insect are reported frequently in some countries of Africa, where those bruchids are endemic (Booker 1967, Germain et al. 1987, Ofuya and Credland 1996, Sanon et al. 2005).

Decellebruchus lunae Romero, sp. n.

Type series

Holotype male, allotype female and two paratypes: M. Elgon, Kenya, 20/I/1979, 1900 m, Palm T. (MZLU), one paratype same data, except 22/I/1979, 2010 m (MZLU). One paratype: Kingsburg beach, Natal, South Africa, 10/IV/1992, O’Brien C.W., L.B. O’Brien & G. Marshall (CEAM).

Description

Male (Fig. 5a–b). Length (pronotum-elytra): 2.0–2.13 mm; width: 1.13–1.25 mm; maximum thoracic depth 1.1–1.2 mm. Color: Antennae with first four segments and apex of last one yellowish, the rest dark or partially dark; body dark, except fore legs, middle legs, elytra, tibiae and tarsi of posterior legs yellowish; however, some specimens may vary from all body yellowish to dark. Vestiture: Body with mixed black, yellowish, and white pubescence; fore coxa with a tuft of white setae; pygidium with basal central spot of white pubescence. Head: Short and broad, densely micropunctulate, frons with a strong median carina, distance between eyes 1.95–2.8× as wide as eye width, eye cleft 0.60–0.71× its length by ocular sinus, posterior margin of eye protruding from adjacent surfaces, postocular lobe rounded and setose; distance from base of antennae to apex of labrum 0.45–0.53× as long as distance from upper limits of eyes to apex of labrum; antennomeres I–III filiform, IV subserrate, V–XI pectinate; antennomere II 2–2.0× as long as antennomere 11; antennomere VII 1.76–2.0× wider that long; antenna extending to mid body. Prothorax: Subconical, without lateral carina; densely foveolate, disc convex, indistinctly gibbous before scutellum and without shallow median channel; prosternal process narrow, triangular, acute, half as long as procoxae. Meso- and metathorax: Scutellum square, bidentate apically; elytra with strial punctures wider than the stria, striae 4 and 5 abbreviated basally by tubercle, humeri slightly raised. Legs: First protarsomere 1.33–1.79× as long as second, first mesotarsomere 2.0–2.1× as long as second, first metatarsomere 2.6–3.2× as long as second; metacoxa densely punctate; hind femur constricted basally and apically, expanded medially to about width of coxa; without external carina ventrally; internal ventral carina with subapical acuminate spine about as long as width of tibial base; hind tibia straight, enlarged, with complete set of carinae; tibial corona with one spinule, the others obsolete, mucro 0.18–0.24× as long as first tarsomere; without sinus at base of spine; first hind tarsomere with ventrolateral glabrous longitudinal carina. Abdomen: Pygidium vertical (Fig. 6); last sternite emarginate. Genitalia: Median lobe moderately long, ventral valve triangular and deeply arcuate, internal sac lined with many small spines, basal portion with a dentiform sclerite and a small spinules forming a triangle (Fig. 7a); lateral lobes elongate, expanded at apex, cleft about 0.73 their length; basal strut with a strong perpendicular keel (Fig. 7b). Female (Fig. 8a–b). Length (pronotum-elytra) 1.85–2.05 mm, width: 1.12–1.3 mm, Maximum thoracic depth 0.95–1.41 mm. Similar to male except antennae serrate; pygidium subvertical; last sternite not marginate.

Figure 5. 

Male habitus of Decellebruchus lunae; a dorsal view b lateral view.

Figure 6. 

Male pygidium of Decellebruchus lunae.

Figure 7. 

Male genitalia of Decellebruchus lunae; a median lobe b lateral lobes.

Figure 8. 

Female habitus of Decellebruchus lunae; a dorsal view b lateral view.

Host plant

Unknown.

Distribution

Kenya and South Africa.

Etymology

The specific epithet honors the grandaughter of the author, Luna Nereida Nila Romero.

Diagnosis

This species is included in the genus Decellebruchus because it presents all characters indicated in the diagnosis of the genus; also it can be separated from the other two species in the genus because the typical male pygidium, less strongly male antennae, unique armature of the internal sac of male genitalia, and lateral lobes of which bear a basal strut with a strong perpendicular keel.

Decellebruchus walkeri (Pic, 1912)

Bruchus figuratus Walker, 1859: 261 (homonymy); Pic 1913: 57; Decelle 1975b: 184; Vazirani 1975: 746; Decelle 1985: 75.

Bruchus walkeri Pic, 1912: 92 (replacement name), 1913: 57; Decelle 1975b: 184; Vazirani 1975: 746; Decelle 1985: 76.

Bruchidius walkeri: Decelle 1975b: 184; Decelle 1985: 75.

Spermophagus figuratus: Motschulsky 1863: 519; Decelle 1975b: 185;

Description

Male (Fig. 9a–b). Length (pronotum-elytra): 1.77–2.1 mm; width: 1.27–1.37 mm; maximum thoracic depth 1.07–1.32 mm. Color: Antennae with the first five segments and apex of the last one yellowish, the rest dark or partially dark; body dark, except fore legs, middle legs, part of elytra, and ventral portion of femora; however some specimens may vary from all body yellowish to dark. Vestiture: Body with mixed black, yellowish, and white pubescence; fore coxa with a tuft of white setae; pygidium with three basal spots of white pubescence, the lateral ones bigger than median. Head: Short and broad, densely micropunctulate, frons with a strong median carina, distance between eyes 1.53–3.3× as wide as eye width, eye cleft 0.57–0.8× its length by ocular sinus, posterior margin of eye protruding from adjacent surfaces, postocular lobe rounded and setose; distance from base of antennae to apex of labrum 0.38–0.47× as long as distance from upper limits of eyes to apex of labrum; antennomeres I–III filiform, IV subserrate, V–XI pectinate; antennomere II 2–2.0× as long as antennomere 11; antennomere VII 4.75–6.67× wider that long; antenna extending to mid body. Prothorax: Subconical, without lateral carina; densely foveolate, disc convex, lightly gibbous before scutellum and without shallow median channel; prosternal process narrow, triangular, acute, half as long as procoxa. Meso- and metathorax: Scutellum square, bidentate apically; elytra with striael punctures as wide as the stria, striae 4 and 5 abbreviated basally by tubercle, humeri slightly raised. Legs: First protarsomere 1.45–1.7× as long as second, first mesotarsomere 1.92–2.6× as long as second, first metatarsomere 2.86–3.4× as long as second; metacoxa densely punctate; hind femur constricted basally and apically, expanded medially to about width of metacoxa; without external carina ventrally; internal ventral carina with subapical acuminate spine about as long as width of tibial base, followed by 2 smaller spines; hind tibia straight, enlarged, with complete set of carinae; tibial corona with 4 spinules, mucro 0.11–0.16× as long as first tarsomere; without sinus at base of spine; first hind tarsomere with ventrolateral glabrous longitudinal carina. Abdomen: Pygidium vertical (Fig. 10); last sternite emarginate. Genitalia: Median lobe moderately long, ventral valve triangular and deeply arcuate, internal sac lined with many small spines, basal portion with a small spinules forming a triangle (Fig. 11a); lateral lobes elongate, expanded at apex, cleft about 0.66 their length; basal strut with small perpendicular keel (Fig. 11b). Female (Fig. 12a–b). Length (pronotum-elytra) 1.95–2.8 mm, width: 1.25–1.8 mm, Maximum thoracic depth 1.12 mm. Similar to male except antennae serrate; pygidium subvertical; last sternite not marginate.

Figure 9. 

Male habitus of Decellebruchus walkeri; a dorsal view b lateral view.

Figure 10. 

Male pygidium of Decellebruchus walkeri.

Figure 11. 

Male genitalia of Decellebruchus walkeri; a median lobe b lateral lobes.

Figure 12. 

Female habitus of Decellebruchus walkeri; a dorsal view b lateral view.

Material examined

INDIA: Maharashtra, Lonavla, 28/IV/2000, 650 m, Pacholatko P. (1 ex., CEAM). KENYA: M. Elgon, 24/I/1979, 1950 m, Palm T. (1 ex., MZLU). SRI LANKA: Vayiriuttu, 5 mi W Trincomalee, Estern Prov., 9/II/1962, Lund University Ceylon Expedition, sweeping at teak plantation (1 ex., MZLU); Kuda Oya, 15 mi S Wellawaya, Uva Prov., 22/III/1962, Brinck, Andersson & Cederholm (2 ex., MZLU); Yakkala, 18 mi NE Colombo Western Prov., 26/III/1926, Brinck, Andersson & Cederholm, swept on vegetation at ditches in paddy fields (1 ex., MZLU).

Host plant

Unknown.

Distribution

India, Kenya, Sri Lanka, Thailand.

Discussion

There is little information about this species. At this time its host plants are unknown and only a few specimens were available for study; three of which were still named Bruchidius walkeri.

Cladistics

A default tree (Fig. 13) and a consensus tree (Fig. 14) were generated with Mesquite (Maddison and Maddison 2015). The shortest and most parsimonius tree obtained with Henning86 using ie- algorithm is shown in Fig. 15. This tree was the shortest and the most parsimonious with a length of 33, consistency index of 87, and retention index of 81. In total, this cladogram was formed by 26 synapomorphies, 8 parallelisms, and 3 reversals. The tree generated with Hennig86 seems the most reliable to explain the phylogenetic hypothesis about of bruchids with pectinate antennae where males and females share the character; however, the consensus tree generated with Mesquite program has similarities with the Hennig86 tree.

Figure 13. 

Default tree generated with Mesquite program.

Figure 14. 

Consensus tree generated with Mesquite program.

Figure 15. 

Phylogenetic tree generated with Hennig86 program.

In the cladogram in Figure 15 can be seen that each one of the clades corresponds to a different taxon of the family Bruchidae and one of the richest in terms of the number of genera was the Acanthoscelidini clade. This cladogram also supports the hypothesis of host preference, for example the species of the clade Pachymerini feed on seeds of the Arecaceae (palms), Megacerini on seeds of the Convolvulaceae, and Acanthoscelidini on seeds of the Fabaceae.

Acknowledgments

I thank the following museum curators: Elizabeth Grobbelaar, South African National Collection of Insects; Paul E. Skelly, Florida State Collection of Arthropods, and Christoffer Fägerström, Musee Zoologique de l’Universite de Lund, Lund University; also Richard L. Westcott, Salem, Oregon, USA and Thomas H. Atkinson, University of Texas for reviewing the manuscript.

References

  • Anton KW (1994) The Bruchidae (Coleoptera) of Saudi Arabia, with descriptions of two new species. Fauna of Saudi Arabia 14: 97–104.
  • Biemont JC, Chauvin G, Germain JF (1982) L’oeuf de Bruchidius atrolineatus (Pic) et son systeme de fixation. Canadian Journal of Zoology 60: 2610–2615. doi: 10.1139/z82-335
  • Blackwelder RE (1946) Checklist of the coleopterous insects of Mexico, Central America, the West Indies, and South America. Bulletin of The United States National Museum 185(4): 551–763. doi: 10.5479/si.03629236.185.4
  • Bondar G (1936) Notas biologicas sobre Bruchideos observados no Brazil. Rio de Janeiro Instituto de Biologia Vegetal. Arquivos 3(1): 7–44.
  • Booker RH (1967) Observations on three bruchids associated with cowpea in northern Nigeria. Journal of Stored Products Research 3: 1–15. doi: 10.1016/0022-474X(67)90082-3
  • Borowiec L (1987) The genera of seed-beetles (Coleoptera, Bruchidae). Polskie Pismo Entomologiczne 57: 3–207.
  • Credland PF (1992) The structure of bruchid eggs may explain the ovicidal effect of oils. Journal of Stored Products Research 28(1): 1–9. doi: 10.1016/0022-474X(92)90025-L
  • Decelle J (1951) Contribution a l”etude des Bruchidae du Congo belge (Coleoptera: Phytophaga). Revue de zoologie et de botanique africaines 45: 172–192.
  • Decelle J (1961) Bruchidae (Coleoptera, Phytophagoidea). Parc National Albert- Mission G. F. Witte (1933–1935) 97(2): 5–10.
  • Decelle J (1975a) Les Coleopteres Bruchides d’Angola. Publicacoes culturais da Companhia de Diamantes de Angola 98: 13–32.
  • Decelle J (1975b) Coleoptera: Bruchidae de Ceylan. Entomologica Scandinavica Supplement 4: 179–194.
  • Decelle J (1985) Synonymies et distribution geographique de Bruchidae (Coleoptera) asiatiques. Bulletin & Annales de la Societe Royale Belge d’Entomologie 121: 75–79.
  • Farris JS (1988) Hennig86 reference. Version 1.5. Documentation.
  • Germain JF, Monge JP, Huignard J (1987) Development of two bruchid populations (Bruchidius atrolineatus (Pic) and Callososbruchus maculatus) (Fab.)) infesting stored cowpea (Vigna unguiculata Walp) pods in Niger. Journal of Stored Products Research 23(3): 157–162. doi: 10.1016/0022-474X(87)90045-2
  • Glitho IA, Huignard J (1990) A histological and ultrastructural comparison of the male accessory reproductive glands of diapausing and non-diapausing adults in Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae). International Journal of Insect Morphology and Embryology 19: 195–209. doi: 10.1016/0020-7322(90)90005-A
  • Hamon C, Biemont JC, Chauvin G (1982) Ultrastructure et fonction secretrice des cellules de la paroi oviductes lateraux chez Acanthoscelides obtectus Say (Coleoptera: Bruchidae). International Journal of Insect Morphology and Embryology 11: 327–339. doi: 10.1016/0020-7322(82)90021-6
  • Huignard J, Monge JP, Germain JF (1989) Influence of thermoperiodic variations on the induction of the reproductive diapause of Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae). In: Tonner M, Soldan T, Bennetova B (Eds) Regulation of Insect Reproductionj. IVAcademia Praha, Praha, 197–207.
  • Ishihara M, Shimada M (1995) Photoperiodic induction of larval diapause and temperature-dependent termination in a wild multivoltine bruchid, Kytorhinus sharpianus. Entomologia Experimentalis et Applicata 75: 127–134. doi: 10.1111/j.1570-7458.1995.tb01918.x
  • Kergoat GJ, Delobel A, Fédière G, Le Rü B, Silvain JF (2005) Both host-plant phylogeny and chemistry have shaped the African seed-beetle radiation. Molecular Phylogenetics and Evolution 35: 602–611. doi: 10.1016/j.ympev.2004.12.024
  • Kingsolver JM (1970) A study of male genitalia in Bruchidae (Coleoptera). Proceedings of the Entomological Society of Washington 72(3): 370–386.
  • Kingsolver JM, Silva P (1991) Update of scientific names of Bruchidae (Coleoptera) listed by Bondar in “Notas Biologicas” (1931 and 1936). Anais da Sociedade Entomologica do Brasil 20(2): 411–415.
  • Kingsolver JM (1988) Pests not known to occur in the United States, or of limited distribution, no. 95: African Cowpea Bruchid with a key to Bruchidae of sored pulses.APHIS-PPQ 81–53, U.S. Department of Agriculture, 1–10.
  • Lenga A, Monge JP, Huignard J (1990) Role des facteurs thermiques dans l’induction de la diapause reproductrice chez Bruchidius atrolineatus Pic (Col: Bruchidae). Regulation des cycles saisonniers chez les Invertebres. Dourdan (France). Ed. INRA, 79–83.
  • Lobl I, Smetana A (2010) Catalogue of Paleartic Coleoptera. Vol. 6. Chrysomeloidea. Apollo Books, 339–353.
  • Luca Y de (1968a) A propos de Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae). Nouvelle description et remarques. Bulletin de l’I.F.A.N. T. XXX, sér. A, 1: 188–199.
  • Luca Y de (1968b) La larve neonate de Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae). Bulletin de l’I.F.A.N. T. XXX, sér. A, 2: 589–592.
  • Monge JP, Germain JF, Huignard J (1988) Importance des variations thermiques sur l’induction de la diapause reproductrice chez Bruchidius atrolineatus Pic (Coleoptere Bruchidae). Acta Oecologica 9(3): 297–307.
  • Monge JP, Lenga A, Huignard J (1989) Induction of reproductive diapause in Bruchidius atrolineatus during the dry season in a Sahelian zone. Entomologia Experimentalis et Applicata 53: 95–104. do: 10.1111/j.1570-7458.1989.tb01292.x
  • Motschulsky TV (1863) Essai d’un catalogue des insectes de I’le Ceylan. Bulletin de la Société Impériale des Naturalistes de Moscou 36: 412–532.
  • Ofuya TI, Credland PF (1996) The Ability of Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae) to infest and damage seeds of different tropical legumes. Journal of Stored Products Research 32(4): 323–328. doi: 10.1016/S0022-474X(97)87176-7
  • Pic M (1912) Renseignements generaux sur les Bruchidae. L’Echange 28: 91–93.
  • Pic M (1913) Bruchidae. Coleopterorum Catalogus. W. Junk, Berlin55: 1–74.
  • Pic M (1921) Diagnoses de Coleopteres exotiques. L’Echange 37: 15–16.
  • Pic M (1932) Nouveautes diverses. Melanges Exotico-Entomologiques 59: 10–36.
  • Pfaffenberger GS (1985) Checklist of selected world species of described first and/or final larval instars. Coleopterists Bulletin 39(1): 1–6.
  • Pfaffenberger GS, Monge JP (1991) Redescription of the larvae of Bruchidius atrolineatus (Pic) (Coleoptera: Bruchidae: Bruchinae). Coleopterists Bulletin 45(4): 309–316.
  • Pichard B, Leroi B, Bonet A (1991) Comparaison des cycles d’Acanthoscelides obtectus et d’A. obvelatus (Coleopteres: Bruchidae) a Tepoztlan (Mexique). Acta Oecologica 12(2): 185–201.
  • Pouzat J, Nammour D (1989) Electrophysiological investigations of sex pheromone reception and release in Bruchidius atrolineatus. Physiological Entomology 14: 319–324.
  • Prevett PF (1961) Field infestation of cowpea (Vigna unguiculata) pods by beetles of the families Bruchidae and Curculionidae in northern Nigeria. Bulletin of Entomological Research 52(4): 635–645. doi: 10.1017/S0007485300055668
  • Prevett PF (1967) Notes on the biology, food plants & distribution of Nigerian Bruchidae (Coleoptera), with particular reference to the northern region. Bulletin of the Entomological Society of Nigeria 1: 3–6.
  • Prevett PF (1971) The larva of some Nigerian Bruchidae (Coleoptera). Transactions of the Royal Entomological Society of London 123(3): 247–312. doi: 10.1111/j.1365-2311.1971.tb00845.x
  • Romero J, Johnson CD (1999) Zabrotes sylvestris, a new species from the United States and Mexico related to Z. subfasciatus (Boheman) (Coleoptera: Bruchidae: Amblycerinae). Coleopterists Bulletin 53(1): 87–98.
  • Sanon A, Dabiré C, Ouedraogo AP, Huignard J (2005) Field occurrence of bruchid pésts of cowpea and associated parasitoids in a sub humid zone of Burkina Faso: Importance on the infestatioon of two cowpea varieties at harvest. Plant Phatology Journal 4(1): 14–20. doi: 10.3923/ppj.2005.14.20
  • Shimada M, Ishihara M (1991) Two types of overwintering larvae in a wild multivoltine bruchid, Kytorhinus sharpianus Bridwell (Coleoptera: Bruchidae). Applied Entomology and Zoology 26(3): 289–297.
  • Shomar NF (1963) A monographic revision of the Bruchidae of Egypt (U.A.R.) (Coleoptera). Bulletin of the Entomological Society of Egypt 47: 141–196.
  • Southgate BJ (1978) The importance of the Bruchidae as pests of grain legumes, their distribution and control. In: Singh SR, van Emden HF, Ajibola TT (Eds) Pests of Grain Legumes: Ecology and Control. Academy Press, London, 219–229.
  • Udayagiri S, Wadhi SR (1989) Catalog of Bruchidae. Memoirs of the American Entomological Institute 45: 1–301.
  • Vazirani TG (1975) A contribution to the knowledge of Oriental Bruchidae. Journal of the Bombay Natural History Society 72(3): 740–757.
  • Walker F (1859) XXVII-Characters of some apparently undescribed Ceylon insects. The Annals and Magazine of Natural History Vol. III, 3rd series: 258–265.
  • Zacher F (1952) Die Nährpflanzen der Samenkäfer. Zeitschrift für angewandte Entomologie 33: 460–480.
login to comment