Ochraethes z-littera ( Chevrolat, 1860 )
publication ID |
https://doi.org/10.5852/ejt.2022.845.1951 |
publication LSID |
lsid:zoobank.org:pub:27631402-ECCF-4C70-A199-D995167F6196 |
DOI |
https://doi.org/10.5281/zenodo.7245686 |
persistent identifier |
https://treatment.plazi.org/id/03D087A5-FFEE-FFCD-9738-2FB4F36A8C82 |
treatment provided by |
Felipe (2022-10-21 13:54:50, last updated by Admin 2024-12-03 22:15:43) |
scientific name |
Ochraethes z-littera ( Chevrolat, 1860 ) |
status |
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Ochraethes z-littera ( Chevrolat, 1860) View in CoL
Clytus (Ochroesthes) z-littera Chevrolat, 1860: 476 View in CoL .
Clytus (Ochroesthes) cristoforii Chevrolat, 1860: 477 View in CoL , syn. nov.
Ochresthes litura Bates, 1885: 298 View in CoL .
Ochraestes z-littera – Thomson 1861: 219.
Ochraesthes cristoforii View in CoL – Thomson 1861: 219.
Ochrestes z-littera View in CoL – Lacordaire 1869: 66.
Ochrestes cristoforii View in CoL – Lacordaire 1869: 66.
Ochresthes z-littera View in CoL – Bates 1880: 51 (distr.); 1885: 297 (distr.).
Ochresthes cristoforii View in CoL – Bates 1880: 51; 1885: 297 (distr.).
Ochresthes citrinus View in CoL – Bates 1885: 297 (error).
Ochraethes z-littera View in CoL – Aurivillius 1912: 386 (cat.). — Blackwelder 1946: 581 (cat.). — Chemsak et al. 1992: 70 (cat.). — Monné 1993: 21 (cat.); 2005: 109 (cat.); 2021: 148 (cat.). — Monné & Giesbert 1994: 116 (cat.). — Noguera & Chemsak 1996: 401 (distr.). — Monné & Hovore 2006; 46 (cat). — Pérez-Flores et al. 2021: 466 (checklist) — Bezark 2021: 74 (checklist).
Ochraethes christofori View in CoL – Aurivillius 1912: 386 (cat.). — Blackwelder 1946: 581 (cat.). — Chemsak et al. 1992: 69 (cat.).
Ochraethes litura View in CoL – Aurivillius 1912: 386 (cat.). — Blackwelder 1946: 581 (cat.). — Chemsak et al. 1992: 69 (cat.). — Monné 1993: 18 (cat.); 2005: 107 (cat.); 2021: 145 (cat.). — Monné & Giesbert 1994: 116 (cat.). — Monné & Hovore 2006: 46 (cat.). — Hovore 2006: 373 (distr.). — Pérez-Flores et al. 2021: 466 (checklist). — Bezark 2021: 73 (checklist).
Ochraethes z-litterata View in CoL – Linsley 1935: 86 (error).
Ochresthes litura View in CoL – Chemsak 1967: 77 (lect.).
Ochraethes cristoforii View in CoL – Monné 1993: 18 (cat.); 2005: 107 (cat.); 2021: 145 (cat.). — Monné & Giesbert 1994: 116 (cat.). — Noguera & Chemsak 1996: 401 (distr.). — Monné & Hovore 2006: 46 (cat.). — Pérez-Flores et al. 2021: 466 (checklist). — Bezark 2021: 73 (checklist).
Ochraethes cristofori View in CoL – Noguera & Chemsak 1996: 401 (cat.).
Chevrolat (1860) described two similar species Ochraethes z-littera View in CoL and O. cristoforii View in CoL . According to Chevrolat´s description of O. z-littera View in CoL : “…sa couleur et les taches du corselet le rapprochent encore du Cl. Cristoforii View in CoL .” (the colour and pattern approaches that of O. cristoforii View in CoL ). Although the coloration in these specimens differ, the transverse Z-shaped band of black pubescence on elytra are almost identical. Bates (1885) described O. litura View in CoL from Guatemala, based on female specimens. In the original description, Bates mentioned that this species resembles O. tomentosus View in CoL , but larger and with elytral apex “oblique sinuate-truncatis”. Here we propose O. cristoforii View in CoL and O. litura View in CoL as junior synonyms of O. z-littera View in CoL based on the following characters: frons strongly transverse ( Fig. 4M–O View Fig ), pronotum with a centrobasal sulcus (pubescence pattern on pronotum is the same in all specimens), patch of yellowish pubescence on first third of elytra, transverse Z-shaped bands of black pubescence on anterior third, and elytral apex with apicolateral spine.
Species delimitation of Ochraethes Chevrolat, 1860
The pubescence pattern on the elytra is the most important character for discriminating the species of Ochraethes ( Linsley 1964) . However, in most species of the genus Ochraethes there is a certain degree of polymorphism, especially in the pubescence (showing tonalities from dark to pale or bright yellow) and integument colour variation ( Fig. 3 View Fig ). The delimitation analyses performed in this study allowed the inference of a slight variation in genetic structure within populations of Ochraethes and the high phenotypic plasticity of their species ( Fig. 3 View Fig ). However, the specimens with extreme range of variation (dark or bright yellow tonalities) are less common, and this fact may be caused by environmental conditions ( Hartl & Clark 1997; Freeland et al. 2011).
The revised material distribution allowed to explore the influence of other extrinsic factor: exposure to heat or humidity. The specimens that inhabit dry environments showed a light coloration on the body, and the specimens in temperate and cold environments showed a darker coloration. This fact has already been studied in other insect groups (e.g. ants, damselflies), and it is linked to heat regulation mechanisms or different behaviors depending on the temperature ( Bishop et al. 2016; Law et al. 2020; Blow et al. 2021). Also, there may be evolutionary factors related to mimicry strategies, as well as camouflage, i.e., the pubescence matching in colour with the flowers on which the adults feed.
Although populations of species of Ochraethes showed a variable coloration of pubescence and integument, they exhibited diagnostic characters throughout their distribution ( Table 1 View Table 1 ). For most of the species analyzed, we included specimens from different localities, and they were delimited as MOTUs with a high degree of variation. Particularly, O. sommeri shows the largest phenotypic plasticity, and two populations commonly considered as O. sommeri were discriminated as independent lineages (representing the two new species). Moreover, the delimitation analyses support synonymies in some species showing morphological similarities and the same distribution.
On the other hand, sexual dimorphism is common in Ochraethes , for example in O. sommeri , females do not show dark tones in the pubescence. Some other species ( O. nigrescens , O. viridiventris ) show a full range of variation in males and females (even in one locality). This is relevant since several species of Ochraethes described in the past were based on single specimens, or used only one sex, and some of them represent only variations of other species. In the descriptions of new species in this group, the type material should at least include specimens of both sexes for a better taxonomic treatment.
A complete morphological revision of the genus Ochraethes will allow the differentiation and boundaries of the genus from other genera of the tribe Clytini , and subsequent nomenclatural changes and keys for species placed in the related genera.
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Bates H. W. 1880. Insecta, Coleoptera, Longicornes. In: Godman F. D & Salvin O. (eds) Biologia Centrali-Americana. Insecta, Coleoptera Vol. 5: 17 - 152. Dulau and Co., London. https: // doi. org / 10.5962 / bhl. title. 730
Bates H. W. 1885 Insecta, Coleoptera, suppl. to Longicornia. In: Godman F. D. & Salvin O. (eds) Biologia Centrali-Americana. Vol. 5: 249 - 436. Dulau and Co., London.
Bezark L. G. 2021. Checklist of the Oxypeltidae, Vesperidae, Disteniidae and Cerambycidae, (Coleoptera) of the Western Hemisphere. Edition 2021. Available from http: // bezbycids. com / byciddb / checklists / WestHemiCerambycidae 2020. pdf [accessed Dec. 2021].
Bishop T. R., Robertson M. P., Gibb H., Van Rensburg B. J., Braschler B., Chown S. L., Foord S. H., Munyai T. C., Okey I., Tshivhandekano P. G., Werenkraut V. & Parr C. L. 2016. Ant assemblages have darker and larger members in cold environments. Global Ecology and Biogeography 25 (12): 1489 - 1499. https: // doi. org / 10.1111 / geb. 12516
Blackwelder R. E. 1946. Checklist of the coleopterous insects of Mexico, Central America, the West Indies and South America. Part 4. Bulletin of the United States National Museum 185: 551 - 763. https: // doi. org / 10.5479 / si. 03629236.185.4
Blow R., Willink B. & Svensson E. I. 2021. A molecular phylogeny of forktail damselflies (genus Ischnura) reveals a dynamic macroevolutionary history of female colour polymorphisms. Molecular Phylogenetics and Evolution 160: 107134. https: // doi. org / 10.1016 / j. ympev. 2021.107134
Chemsak J. A. 1967. Lectotype designations of Cerambycidae in the British Museum (Natural History). Journal of the Kansas Entomological Society 40 (1): 73 - 81.
Chemsak J. A., Linsley E. G. & Noguera F. A. 1992. Listados Faunisticos de Mexico II. Los Cerambycidae y Disteniidae de Norteamerica, Centroamerica y las Indias Occidentales. Instituto de Biologia, Universidad Nacional Autonoma de Mexico, Mexico.
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Freeland J. R., Kirk H. & Petersen S. 2011. Molecular Ecology. Second edition. Wiley-Blackwell, Hoboken, New Jersey. https: // doi. org / 10.1002 / 9780470979365
Hartl D. L. & Clark A. G. 1997. Principles of Population Genetics. Fourth edition. Sinauer Associates, Inc. Sunderland, Massachusetts.
Hovore F. T. 2006. The Cerambycidae (Coleoptera) of Guatemala. In: Cano E. (ed.) Biodiversidad de Guatemala, Vol. 1: 363 - 378. Universidad del Valle de Guatemala, Guatemala.
Lacordaire J. T. 1869. Histoire naturelle des Insectes. Genera des Coleopteres, ou expose methodique et critique de tous les genres proposes jusqu'ici dans cet ordre d'insectes. Vols 8 and 9. Paris. Librairie Encyclopedique de Roret. https: // doi. org / 10.5962 / bhl. title. 8864
Law S. J., Bishop T. R., Eggleton P., Griffiths H., Ashton L. & Parr C. 2020. Darker ants dominate the canopy: testing macroecological hypotheses for patterns in colour along a microclimatic gradient. Journal of Animal Ecology 89 (2): 347 - 359. https: // doi. org / 10.1111 / 1365 - 2656.13110
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Linsley E. G. 1964. The Cerambycidae of North America. Part V. Taxonomy and Classification of the Subfamily Cerambycinae, Tribes Callichromini through Ancylocerini. University of California Press, California.
Monne M. A. 1993. Catalogue of the Cerambycidae (Coleoptera) of the Western Hemisphere. Part IX. Subfamily Cerambycinae: Tribes Clytini, Anaglyptini, Tillomorphini and Cleomenini. Sociedade Brasileira de Entomologia, Sao Paulo.
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Fig. 4.Head, frontal view of type species of Ochraethes. A. Ochraethes brevicornis (Chevrolat, 1860),♀. B. O. virescens (Chevrolat, 1860), ♂. C. O. cinereolus (Bates, 1892) comb. nov., ♀. D. O. octomaculata Chemsak & Noguera, 2001, ♂. E. O. obliquus (Chevrolat, 1860), ♂. F. O. zebratus Bates, 1885, ♀. G. O. sommeri (Chevrolat, 1835), ♂. H. O. circuliferus (Chevrolat, 1860) (= Ochraethes sommeri), ♀. I. Trichoxys giesberti Botero et al., 2019, ♀. J. O. viridiventris (Chevrolat, 1860), ♂. K. O. nigritus Bates, 1892 (= Ochraethes viridiventris), ♂. L. O. clerinus Bates, 1892, ♀. M. O. z-littera (Chevrolat, 1860), ♂. N. O. cristoforii (Chevrolat, 1860), ♂. O. O. litura Bates, 1885, ♀.
Fig. 3. Pubescence variation on the elytra in Ochraethes Chevrolat, 1860. A–B. Ochraethes brevicornis (Chevrolat, 1860) (♀, ♂). C–E. O. cinereolus (Bates, 1892) comb. nov. (♂, ♂, ♀). F–I. O. obliquus (Chevrolat, 1860) (♂, ♂, ♀, ♀). J–N. O. sommeri (Chevrolat, 1835) (♂, ♂, ♂, ♀, ♀). O–S. O. viridiventris (Chevrolat, 1860) (♂, ♀, ♂, ♂, ♀). T–X. O. z-littera (Chevrolat, 1860) (♂, ♂, ♂, ♀, ♀).
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.
Kingdom |
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Class |
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Order |
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Polyphaga |
SuperFamily |
Chrysomeloidea |
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SubFamily |
Cerambycinae |
Tribe |
Clytini |
Genus |
Ochraethes z-littera ( Chevrolat, 1860 )
Pérez-Flores, Óscar & Toledo-Hernández, Víctor H. 2022 |
Ochraethes cristofori
Noguera F. A. & Chemsak J. A. 1996: 401 |
Ochraethes cristoforii
Perez-Flores O. & Toledo-Hernandez V. H. & Bezark L. G. & Monne M. A. 2021: 466 |
Bezark L. G. 2021: 73 |
Monne M. A. & Hovore F. T. 2006: 46 |
Noguera F. A. & Chemsak J. A. 1996: 401 |
Monne M. A. & Giesbert E. F. 1994: 116 |
Monne M. A. 1993: 18 |
Ochresthes litura
Chemsak J. A. 1967: 77 |
Ochraethes z-litterata
Linsley E. G. 1935: 86 |
Ochraethes z-littera
Perez-Flores O. & Toledo-Hernandez V. H. & Bezark L. G. & Monne M. A. 2021: 466 |
Bezark L. G. 2021: 74 |
Noguera F. A. & Chemsak J. A. 1996: 401 |
Monne M. A. & Giesbert E. F. 1994: 116 |
Monne M. A. 1993: 21 |
Chemsak J. A. & Linsley E. G. & Noguera F. A. 1992: 70 |
Blackwelder R. E. 1946: 581 |
Aurivillius C. 1912: 386 |
Ochraethes christofori
Chemsak J. A. & Linsley E. G. & Noguera F. A. 1992: 69 |
Blackwelder R. E. 1946: 581 |
Aurivillius C. 1912: 386 |
Ochraethes litura
Perez-Flores O. & Toledo-Hernandez V. H. & Bezark L. G. & Monne M. A. 2021: 466 |
Bezark L. G. 2021: 73 |
Monne M. A. & Hovore F. T. 2006: 46 |
Hovore F. T. 2006: 373 |
Monne M. A. & Giesbert E. F. 1994: 116 |
Monne M. A. 1993: 18 |
Chemsak J. A. & Linsley E. G. & Noguera F. A. 1992: 69 |
Blackwelder R. E. 1946: 581 |
Aurivillius C. 1912: 386 |
Ochresthes litura
Bates H. W. 1885: 298 |
Ochresthes citrinus
Bates H. W. 1885: 297 |
Ochresthes z-littera
Bates H. W. 1880: 51 |
Ochresthes cristoforii
Bates H. W. 1885: 297 |
Bates H. W. 1880: 51 |
Ochrestes z-littera
Lacordaire J. T. 1869: 66 |
Ochrestes cristoforii
Lacordaire J. T. 1869: 66 |
Ochraestes z-littera
Thomson J. 1861: 219 |
Ochraesthes cristoforii
Thomson J. 1861: 219 |
Clytus (Ochroesthes) z-littera
Chevrolat L. A. A. 1860: 476 |
Clytus (Ochroesthes) cristoforii
Chevrolat L. A. A. 1860: 477 |
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