Scybalocanthon Martínez, 1948

Silva, Fernando A. B. & Valois, Marcely, 2019, A taxonomic revision of the genus Scybalocanthon Martínez, 1948 (Coleoptera Scarabaeidae: Scarabaeinae: Deltochilini), Zootaxa 4629 (3), pp. 301-341 : 304-306

publication ID

https://doi.org/ 10.11646/zootaxa.4629.3.1

publication LSID

lsid:zoobank.org:pub:1D47B452-0A40-4BC5-9BBA-C06DEB298C9A

DOI

https://doi.org/10.5281/zenodo.4335165

persistent identifier

https://treatment.plazi.org/id/9D12E557-3A5A-FF9B-95F1-FC25FB8BC339

treatment provided by

Felipe

scientific name

Scybalocanthon Martínez, 1948
status

 

Scybalocanthon Martínez, 1948 View in CoL

Scybalocanthon Martínez, 1948: 4 View in CoL (original description); Martínez 1949: 188–189 (taxonomic remarks and identification key); Pereira & Martínez 1956: 96, 114, 184 (catalog and identification key); Halffter 1958: 207 (classification); Halffter 1961: 231 (identification key); Vulcano & Pereira 1964: 637 (catalog); Halffter & Mathews 1966: 261 (catalog, distribution); Vulcano & Pereira 1967: 549 (identification key); Halffter & Martínez 1977: 17, 38, 67, 68 (identification key and diagnosis); Halffter & Edmonds 1982: 139 (catalog, distribution); Medina & Lopera-Toro 2000: 311 (identification key); Vaz-de-Mello 2000: 194–195 (checklist); Medina et. al. 2001: 137 (checklist); Medina et al. 2003: 65 (systematic of Canthon View in CoL and related genera, distribution); Hamel-Leigue et. al. 2006: 15 (checklist); Monaghan et al. 2007: 9 (phylogenetic hypothesis to the Scarabaeinae View in CoL ); Molano & Medina 2010: 689 (description of the variation of the male genitalia); Vaz-de-Mello et al. 2011: 6, 11, 19, 26, 34, 41, 45, figs. 154–155 (identification key to the New World genera and subgenera of Scarabaeinae View in CoL dung beetles); Carvajal et. al. 2011: 116, 314 (checklist); Solís et al. 2011: 36 (checklist); Solís & Kohlmann 2012: 3 (cited as a junior synonym of Canthon View in CoL ); Boilly & Vaz-de-Mello 2013: 108 (identification key); Tarasov & Génier 2015: 21 (phylogenetic hypothesis to the Scarabaeinae View in CoL tribes); Tarasov & Dimitrov 2016: 15 (new concept for Deltochilini View in CoL ); Vaz-de-Mello & Silva 2017: 144–145 View Cited Treatment (identification key to the species from South America south of the Amazon basin); Cupello & Vaz-de- Mello 2018: 15, 18, 34, 47, 54; Chamorro et al. 2018: 76, 98 (identification key, checklist to the genera and species from Ecuador); Chamorro et al. 2019: 10, 229, 263 (catalog, checklist to the genera and species from Ecuador).

Canthon (Scybalocanthon) : Krajcik 2006: 25 (catalog); Krajcik 2012: 63 (catalog).

Type species. Canthon moniliatus Bates, 1887 View in CoL by original designation ( Martínez 1948: 6).

Diagnosis. Within Deltochilini (sensu Tarasov & Dimitrov 2016) , Scybalocanthon can be distinguished by several characters. Mesotarsomeres and metatarsomeres short, external margin approximately half the length of the second tarsomere, and obliquely truncate apically ( Figs. 3 View FIGURE 3 G–H). Lateral margins of tarsomeres parallel, forming an even margin along the length of the tarsus. Overall shape of mesotarsomeres and metatarsomeres 2–4 varies from quadrate to rectangular. Dorsal surface of mesotibiae with dense setae, randomly distributed ( Fig. 3I View FIGURE 3 ); setae not aligned as in some Canthon species ( Fig. 3J View FIGURE 3 ). Pygidium and propygidium not separated by carina, or carina inconspicuous.

Description. Body. Coloration variable according to species. Oval shape, lateral edges rounded. Length. 5.8– 10.3 mm. Head. Dorsal surface with fine microgranulation. Clypeal margin with two small, triangular central teeth. Lateral margin regularly curved outward. Eye comma shaped in dorsal view. Dorsal interocular space at least 12 times as wide as eyes. Thorax. Pronotum twice as wide as long, anterior angles acute, directed forward. Margin between anterior and posterior angles slightly or strongly curved outward, with or without angulation at the middle portion. Surface of pronotum with color pattern variable according to species. Hypomera not excavated, lacking carina separating the anterior and posterior portions, or with short and inconspicuous carina. Mesometaventral suture straight or slightly arched. Metaventrite moderately convex. Elytra. Lateral margin slightly curved outward or approximately straight. Elytral striae weakly ( Fig. 3B View FIGURE 3 ) or strongly ( Fig. 3A View FIGURE 3 ) impressed, with punctures conspicuous or not. Surface of elytra with color pattern variable according to species. Eighth stria carinate ( Fig. 3D View FIGURE 3 ) or not at the anterior portion. Abdomen. Pygidium rounded apically, not separated from propygidium by carina, or carina inconspicuous. Surface of pygidium with color pattern variable according to species. Legs. Surface with uniform coloration or with yellow and black spots along its length ( Figs. 3 View FIGURE 3 E–F). Protibiae with three lateral teeth. Anterior and posterior edge of mesofemora and metafemora not margined. Mesotibiae smoothly arched toward body. Metatibiae almost straight. First mesotarsomeres and metatarsomeres short, external margin approximately half the length of the second tarsomere, obliquely truncate at the apex ( Figs. 3 View FIGURE 3 G–H). Tarsal claws without basal teeth. Secondary sexual characters. Females can be distinguished from males, in general, by the middle protibial tooth equidistant from the other teeth; in males, the middle protibial tooth is closer to apical tooth. Apex of protibial teeth and tibial spur more pointed than that of males. Sixth abdominal ventrite longer than in males. The anterocentral portion of sixth abdominal ventrite, in the lateral view, more swollen than the posterocentral portion (males have, in general, the posterocentral portion more swollen). S. cyanocephalus and S. arnaudi new species do not show the sexual dimorphism discussed above (i.e., the differences concerning the protibial teeth, the protibial spur and the sixth ventrite). Genital capsule. Parameres slightly to strongly asymmetrical; dorsal margin with or without projection; ventral margin can have an excavation at the basal portion (as Fig. 4S View FIGURE 4 ). Endophallus. Lamella copulatrix absent. Superior right peripheral (SRP) sclerite circular, with handle-shaped extension and ring with thin border ( Figs. 5 View FIGURE 5 A–W). Frontolateral peripheral (FLP) sclerite with variable shape according to species ( Figs. 5 View FIGURE 5 A–W). Complex of axial and subaxial (A+SA) sclerites elongate, with irregular shape; in some species there can be one short additional sclerite ( AS) attached to the larger sclerite ( Figs. 5 View FIGURE 5 A–W).

Taxonomic remarks. According to Martínez (1948), in his original description of the genus, the main characters that separate Scybalocanthon from Canthon are the first mesotarsomeres and metatarsomeres notably shorter than the second; the shape of mesotarsomeres and metatarsomeres; the tooth on the outer edge of protibiae; protibial spur not differentiated between males and females; and the shape of labium. Martínez (1948) did not accurately stated how much shorter the first mesotarsomeres and metatarsomeres are in relation to the second, rendering this characteristics ambiguous for a long time. Martínez & Halffter (1972), for instance, described Scybalocanthon balachowskyi and stated that the first mesotarsomeres are “faintly shorter than second”. Molano & Medina (2010) compared the morphology of this character among several Scybalocanthon species and pointed out that, in general, the second mesotarsomeres and metatarsomeres are twice the length of the first. According to these authors, the second mesotarsomeres and metatarsomeres are 1.5 times the length of the first only in S. arcabuquensis and S. nigellus . Vaz-de-Mello et al. (2011), in their identification key to the genera and subgenera of Scarabaeinae of the New World, stated the following for Scybalocanthon : “Basal tarsomere of mesotarsus and metatarsus short, length about one-half that of second tarsomere, obliquely (nearly 45º) truncate apically. Lateral borders of tarsomeres parallel, forming a continuous border for all tarsi, overall shape of tarsomeres 2‒4 quadrate to rectangular”. Although Molano & Medina (2010) stated that most of Scybalocanthon species have the second mesotarsomeres and metatarsomeres with at least twice the length of the first, they described a species in which the second mesotarsomeres and metatarsomeres were about 1.5 times the length of the first only. Molano & Parrales (2015) also described a species ( S. magnus ) that has subequal first and second mesotarsomeres and metatarsomeres.

Scybalocanthon , as defined here, comprises only species with the following combination of characters: second mesotarsomeres and metatarsomeres with external margin with twice the length of the first tarsomeres, the latter with apex obliquely truncate ( Figs. 3 View FIGURE 3 G–H); lateral borders of tarsomeres parallel, forming a continuous border for all tarsi, overall shape of tarsomeres 2‒4 quadrate to rectangular; and dorsal/internal surface of mesotibiae with dense, randomly distributed setae ( Fig. 3I View FIGURE 3 ). The latter character is proposed herein to establish a more precise genus limit in combination with the other characters mentioned above. Some species currently included in Scybalocanthon , however, have the second mesotarsomeres and metatarsomeres with external margin approximately 1.5 times the length of the first tarsomere, or shorter; lateral margins of mesotarsomeres and metatarsomeres 2-4 divergent apically, not forming a continuous border for all tarsi; and/or dorsal/internal surface of mesotibiae with setae arranged in rows. Therefore, these species were removed from Scybalocanthon and considered as incertae sedis within the genus Canthon : Canthon arcabuquensis ( Molano & Medina, 2010) new combination, Canthon balachowskyi ( Martínez & Halffter, 1972) new combination, Canthon nigellus Schmidt, 1922 , Canthon luctuosus Harold, 1868 , and Canthon magnus ( Molano & Parrales, 2015) new combination.

The taxonomy of the genus Canthon is still problematic. Throughout its taxonomic history, more than 250 species have been described in this genus ( Krajcik 2012), but its precise limits have not been established. Over the last decades, attempts tried to reduce the great heterogeneity and artificiality of Canthon . Several new species were described and the genus was divided into a large number of taxa (nine subgenera and 28 full genera) ( Halffter & Martínez 1977; see also Cupello & Vaz-de-Mello 2018). Cupello & Vaz-de-Mello (2018) suppose that the taxa considered by Halffter & Martínez (1977) as subgenera of Canthon will eventually turn out as independent genera, since there is no known synapomorphy. Currently, most Canthon species are assigned to one of the nine subgenera, but 29 species and subspecies have not been hitherto classified in the last taxonomic revision of the genus ( Halffter & Martínez 1977; Schoolmeesters 2017). For those species, Halffter & Martínez (1977) formed groupings called “species lines”, some of which with subgroups. Since then, these species have been regarded as incertae sedis.

In this work, the four species removed from Scybalocanthon are considered as incertae sedis within Canthon . They do not present diagnostic characteristics that allow us to classify them into other genera closely related to Canthon ( Halffter & Martínez 1977; Vaz-de-Mello et al. 2011). At the same time, these species match the definition of Canthon given by Halffter & Martínez (1977). According to the identification key to genera and subgenera of Scarabaeinae from the New World ( Vaz-de-Mello et al. 2011), these species are also identified as Canthon . In addition, Canthon was the genus in which two of those species were previously placed ( C. nigellus and C. luctuosus ). Future cladistic studies may unravel the deeper relationships between those and other species of Canthon sensu lato, but we prefer to transfer temporarily those four species to this genus.

The genus Scybalocanthon , as defined here, includes 23 valid species that are primarily distributed in South America, with one species, S. moniliatus ( Bates, 1887) , reaching as far north as Central America. The highest known species richness occurs in Brazil (11 species), Ecuador (8), and Colombia (6) ( Figs. 6 View FIGURE 6 A–F).

The male genitalia present important characters used to recognize and delimit species within the genus. The most relevant characters are the asymmetry and shape of the left and right parameres, the presence or absence of sets of bristles or microbristles right beside the FLP sclerite, and the number of these sets of bristles. The parameres asymmetry is an important evolutionary character of the genus. This asymmetry may be light or strong. When the asymmetry is light, the parameres have a similar shape and the lengths are slightly different ( Figs. 4 View FIGURE 4 A–H, J–N, P–Q, S, U–V). However, if the asymmetry is strong, the shape of the parameres is completely different from one another ( Figs. 4I, O, R, T, W View FIGURE 4 ). The morphology and size of the FLP can vary within the genus, from an elongate ( Figs. 5 View FIGURE 5 A–G, I–K, M, O, U–V) to a short and truncate shape ( Figs. 5L, P, H, N, Q View FIGURE 5 , S–T, W). An additional sclerite ( AS) can be found between the sclerites of the A+SA complex and the FLP in some species (as Fig. 5B View FIGURE 5 ).

Some characters of external morphology can vary within the same species, such as body coloration and patterns of spots. In addition, some species such as S. arnaudi new species, S. federicoescobari new species S. martinezi new species, S. papaxibe new species, S. pinopterus , and S. uniplagiatus present similar external morphology, which makes it difficult to recognize these species without examining the male genitalia.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Coleoptera

Family

Scarabaeidae

Loc

Scybalocanthon Martínez, 1948

Silva, Fernando A. B. & Valois, Marcely 2019
2019
Loc

Canthon (Scybalocanthon)

Krajcik, M. 2012: 63
Krajcik, M. 2006: 25
2006
Loc

Scybalocanthon Martínez, 1948: 4

Chamorro, W. & Marin-Armijos, D. & Asenjo, A. & Vaz-de-Mello, F. Z. 2019: 10
Chamorro, W. & Marin-Armijos, D. & Granda, V. & Vaz-de-Mello, F. Z. 2018: 76
Vaz-de-Mello, F. Z. & Silva, F. A. B. 2017: 144
Tarasov, S. I. & Dimitrov, D. 2016: 15
Tarasov, S. I. & Genier, F. 2015: 21
Boilly, O. & Vaz-de-Mello, F. Z. 2013: 108
Solis, A. & Kohlmann, B. 2012: 3
Vaz-de-Mello, F. Z. & Edmonds, W. D. & Ocampo, F. C. & Schoolmeesters, P. 2011: 6
Solis, C. & Noriega, J. A. N. & Herrera, G. 2011: 36
Molano R. & Medina, C. A. 2010: 689
Monaghan, M. T. & Inward, D. J. G. & Hunt, T. & Vogler, A. P. 2007: 9
Medina, C. A. & Scholtz, C. H. & Gill, B. D. 2003: 65
Medina, C. A. & Lopera-Toro, A. 2000: 311
Vaz-de-Mello, F. Z. 2000: 194
Halffter, G. & Edmonds, W. D. 1982: 139
Halffter, G. & Martinez, A. 1977: 17
Vulcano, M. A. & Pereira, F. S. 1967: 549
Vulcano, M. A. & Pereira, F. S. 1964: 637
Halffter, G. 1961: 231
Halffter, G. 1958: 207
Pereira, F. S. & Martinez, A. 1956: 96
Martinez, A. 1949: 188
Martinez, A. 1948: 4
1948
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