Biodiversity Data Journal :
Taxonomic Paper
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Corresponding author: Oscar Pérez-Flores (oscar_skopt@ciencias.unam.mx)
Academic editor: Jennifer C. Girón Duque
Received: 19 May 2020 | Accepted: 09 Jul 2020 | Published: 16 Jul 2020
© 2020 Oscar Pérez-Flores, Víctor Toledo-Hernández
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Pérez-Flores O, Toledo-Hernández VH (2020) Diversity of the longhorned beetles (Coleoptera: Cerambycidae) from Cuatro Ciénegas Basin, Coahuila, Mexico. Biodiversity Data Journal 8: e54495. https://doi.org/10.3897/BDJ.8.e54495
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Cerambycidae is one the most diverse families in the order Coleoptera with more than 37,000 species described in all continents. Cerambicyd beetles have a worldwide distribution from sea level to montane sites. In Mexico, more than 1,600 species have been recorded. Nevertheless, the diversity and distribution of this family in the Mexican deserts is poorly known.
A first checklist of Cerambycidae from seven localities of Cuatro Ciénegas Basin is presented. This study is the result of sampling carried out between 2009 to 2013. Some material from other collections is also included. The species list includes four subfamilies, 13 tribes, 32 genera and 37 species, from which 13 are new records for the state of Coahuila and three species represent new records for Mexico. These results highlight the paucity of knowledge of insects in the deserts of Mexico.
Cerambycid beetles, Chihuahuan desert, distribution, North America.
Cerambycidae comprise one of the largest families of Coleoptera, represented by more than 37,000 species, described in more than 5,300 genera from eight subfamilies (
The Cuatro Ciénegas Basin (CCB) (
The fauna that occurs in the CCB is a mixture of species with Neotropical and Nearctic biogeographic origins or affinities. This important region of transition can represent the distributional limits of both groups (
The dominant habitat in CCB is desertic shrub of the microphyle and rosetophyle variants, which include sotol, mesquite, secondary grassland and semi-aquatic vegetation associated with ponds. The climate is desertic dry (BW) (
Fourteen field trips were performed during 2012 and 2013. Records from sporadic trips in 2009 and 2010 are also included. Sampling totalled 84 collecting days with at least three people collecting each day (09:00 to 16:00 h). Different sampling techniques (direct and indirect) were applied: by hand, sweep net and light traps. Cerambycid beetles were identified to species level with specialised literature (
Cercidium microphyllum Rose and I. M. Johnston (Caesalpiniaceae), Quercus sp. (Fagaceae), Prosopis juliflora (Swartz) de Candolle (Mimosaceae), Morus rubra Linnaeus (Moraceae), Citrus sp. (Rutaceae), Populus sp. (Salicaceae), Ulmus sp. (Ulmaceae), Vitis sp. (Vitaceae). (Monné 2020)
MZ-FC
Pinus pseudostrobus Lindley, P. rudis Endlicher (Pinaceae). (Monné 2020)
MEXICO: Ciudad de México, Coahuila (new state record), Guerrero, Hidalgo, México, Michoacán, Morelos, Nuevo León, Veracruz; GUATEMALA.
Celtis reticulata Torr. (Cannabaceae), Prosopis juliflora (Swartz) de Candolle, Senegalia greggii A. Gray (Mimosaceae). (Monné 2020)
USA: California, Texas; MEXICO: Baja California Norte, Coahuila (new state record), Sinaloa, Sonora.
Acer rubrum Linné (Aceraceae), Celtis laevigata Willdnow (Cannabaceae), Juniperus virginiana Linné (Cupressaceae), Diospyros virginiana Linné (Ebenaceae), Quercus sp. (Fagaceae), Carya glabra (Miller) Sweet, C. illinoinensis (Wangenheim) K. Koch, C. ovata (Miller) K. Koch, C. tomentosa Nuttall (Juglandaceae), Pinus contorta Douglas ex Loudon, P. resinosa Aiton (Pinaceae), Ulmus sp. (Ulmaceae). (Monné 2020)
Baccharis neglecta Nuttall (Asteraceae), Acacia hindsii Bentham, Prosopis dulcis Kunth, P. juliflora (Swartz) de Candolle (Mimosaceae), Condalia globosa I. M. Johnston (Rhamnaceae), Crataegus pubescens Steudel, Malus sylvestris Miller, Prunus capollin Zuccarini, P. domestica Linné, P. persica (Linné) Batsch, Pyrus communis Willdenow (Rosaceae). (Monné 2020)
Acacia sp. (Mimosaceae). (Monné 2020)
Acacia berlandieri Bentham (Mimosaceae). (Monné 2020)
Rhus aromatica Aitchison (Anacardiaceae), Baccharis sarothroides A. Gray (Asteraceae), Quercus sp. (Fagaceae). (Monné 2020)
Rhus aromatica Aitchison (Anacardiaceae), Grindelia sp. (Asteraceae), Celtis laevigata Willdenow, C. lindheimeri Engelmann, C. reticulata Torrey (Cannabaceae), Sophora secundiflora (Ortega) de Candolle (Fabaceae), Quercus sp. (Fagaceae), Juglans nigra Linnaeus (Juglandaceae), Pithecellobium flexicaule (Bentham) Coulter, Prosopis juliflora (Swartz) de Candolle, Vachellia rigidula (Bentham) Seigler and Ebinger, (Mimosaceae), Morus rubra Linnaeus (Moraceae), Pinus cembroides Zuccarini (Pinaceae), Zanthoxylum clava-herculis Linnaeus (Rutaceae). (Monné 2020)
Quercus grisea Liebmann (Fagaceae). (Monné 2020)
Celtis reticulata Torrey (Cannabaceae), Dermatophyllum secundiflorum (Ortega) Gandhi and Reveal (Fabaceae). (Monné 2020)
Dalea formosa Torrey (Fabaceae). (Monné 2020)
Baccharis halimifolia Linnaeus (Asteraceae), Acacia rigidula Bentham, Leucaena sp., Prosopis juliflora (Swartz) de Candolle, Vachellia farnesiana (Linnaeus) Wight and Arn., V. rigidula (Benth.) Seigler and Ebinger (Mimosaceae). (Monné 2020)
Acacia constricta Bentham ex Gray, Prosopis juliflora (Swartz) de Candolle (Mimosaceae). (Monné 2020)
Berberis harrisoniana Kearney and Peebles (Berberidaceae), Juniperus deppeana Steudel (Cupressaceae), Juglans major A. A. Heller (Juglandaceae), Salix sp. (Salicaceae). (Monné 2020)
Baccharis neglecta Nuttall (Asteraceae), Celtis berlandieri Klotzsch (Cannabaceae), Diospyros texana Scheele (Ebenaceae), Eysenhardtia polystachya (Ortega) Sargent, E. texana Scheele (Fabaceae), Pithecellobium flexicaule (Bentham) Coulter, P. pallens (Bentham) Standley (Mimosaceae), Citrus sinensis (Linnaeus) Osbeck, Zanthoxylum fagara (Linnaeus) Sargent (Rutaceae). (Monné 2020)
Lysiloma acapulcense (Kunth.) Benth., Haematoxylum brasiletto H. Karst., Vachellia pennatula (Schltdl. and Cham.) Seigler and Ebinger (Fabaceae). (Monné 2020)
Chrysothamnus viscidiflorus (Hooker) Nuttall, Gutierrezia longifolia Greene, G. lucida Greene, G. wrightii A. Gray, Haplopappus hartwegi (Gray) Blake, H. pluriflorus (Gray) Hall, Xanthocephalum glutinosum (Sprengel) Shinners, X. sarothrae (Pursh) Shinners (Asteraceae). (Monné 2020)
Helianthus sp., Verbesina sp., Viguiera sp. (Asteraceae). (Monné 2020)
Prosopis juliflora (Swartz) de Candolle, Vachellia farnesiana (Linnaeus) Wight and Arn. (Mimosaceae). (Monné 2020)
Baccharis sp. (Asteraceae), Cassia sp. (Caesalpiniaceae), Leucaena pulverulenta (Schlechtendal) Bentham, Prosopis juliflora (Swartz) de Candolle, Vachellia farnesiana (Linnaeus) Wight and Arn. (Mimosaceae), Ficus sp. (Moraceae), Coffea arabica Linnaeus (Rubiaceae), Ulmus crassifolia Nuttall (Ulmaceae). (Monné 2020)
Acacia berlandieri Bentham, Prosopis juliflora (Swartz) de Candolle (Mimosaceae). (Monné 2020)
Sphaeralcea sp. (Malvaceae). (Monné 2020)
Astrophytum asterias (Zuccarini) Lemaire, Homalocephala texensis Britton and Rose, Marginatocereus marginatus (de Candolle) Beckeberg, Opuntia arborescens Engelmann, O. arbuscula Engelmann, O. engelmanni Salm-Dyck, O. imbricata de Candolle, O. leptocaulis de Candolle, O. lindheimeri Engelmann, O. macrocentra Engelmann, O. megacantha Salm-Dyck, O. robusta Wendland, O. spinosior Toumey, O. violacea Engelmann, Platyopuntia sp. (Cactaceae). (Monné 2020)
Parkinsonia aculeata Linnaeus (Caesalpiniaceae), Casuarina cuninghamiana Miquel (Casuarinaceae), Sarcobatus vermiculatus (Hooker) Torrey (Chenopodiaceae), Acacia greggii A.Gray, Mimosa sp., Pithecellobium flexicaule (Bentham) Coulter, Prosopis juliflora (Swartz) de Candolle, P. glandulosa Torrey, Vachellia farnesiana (Linnaeus) Wight. and Arn. (Mimosaceae). (Monné 2020)
As this study is the first species list of Cerambycidae fauna in a Mexican desert environment, it greatly increases the knowledge of this group in Mexico. We recorded 37 species from 32 genera and identified 13 tribes from four subfamilies (Prioninae, Lepturinae, Cerambycinae and Lamiinae) Table
Despite the fact that Mexico has extensive area of deserts, faunistic studies relating to Cerambycidae have previously not been conducted in this or similar xerophilous habitats. In Mexico, the family Cerambycidae has been studied mainly in tropical dry forest (e.g.
Of the species recorded in this study, Meloemorpha aliena (Bates), Knulliana cincta cincta (Drury), Megacyllene antennata (White), Aneflomorpha rectilinea rectilinea Casey, Anopliomorpha rinconia (Casey), Neaneflus brevispinus Chemsak, Haplidus laticeps Knull, Methia mormona Linell, Rhopalophora angustata Schaeffer, Euderces basimaculatus Giesbert & Chemsak, Crossidius suturalis suturalis LeConte, Plionoma suturalis (LeConte) and Stenaspis solitaria (Say) are new records for the state of Coahuila. Typocerus sinuatus (Newman), Neoclytus mucronatus mucronatus (Fabricius) and Aneflomorpha werneri Chemsak are reported for the first time in Mexico. These three species have been previously recorded in the southern United States (Texas).
Possibly due in part to extensive collecting efforts, the states of Veracruz (406), Oaxaca (343), Jalisco (327) and Chiapas (315) (
The distribution of species that were recorded in CCB shows a mixture between cerambycid species with distributional records in United States and Mexico (
The CCB is a unique region with different components from Neotropical and Nearctic biogeographic provinces. This makes it an essential crossroads to understand the evolution of several faunal groups (
The authors thank M. Trujano-Ortega and U. García-Vázquez for providing the material to realise this study; CONABIO (JF065) to A. Nieto, for fieldwork; WWF-Alianza Carlos Slim (L039) and the Theodore Roosevelt Memorial Fund (American Museum of Natural History) for resources provided to M. Trujano-Ortega and U. García-Vázquez. We also thank PRONATURA A. C., DESUVALLE A.C. and CONANP for their assistance with fieldwork and C. Mayorga (CNIN-IBUNAM) for allowing access to the collections under their care. We would also like to thank Hans Clebsch for comments on the manuscript and helping to improve its English content.