2urn:lsid:arphahub.com:pub:45048D35-BB1D-5CE8-9668-537E44BD4C7Eurn:lsid:zoobank.org:pub:91BD42D4-90F1-4B45-9350-EEF175B1727AZooKeysZK1313-29891313-2970Pensoft Publishers10.3897/zookeys.721.2152921529Research ArticleChactidaeScorpionesSystematicsEcuadorThe geographical patterns of distribution of the genus Teuthraustes Simon, 1878 in Ecuador and description of three new species (Scorpiones, Chactidae)YthierEriceythier@syntechresearch.com1LourençoWilson R.2SynTech Research, 613 route du Bois de Loyse, 71570 La Chapelle de Guinchay, FranceUnaffiliatedLa Chapelle de GuinchayFranceMuséum national d’Histoire naturelle, Sorbonne Universités, Institut de Systématique, Evolution, Biodiversité (ISYEB), UMR7205-CNRS, MNHN, UPMC, EPHE, CP 53, 57 rue Cuvier, 75005 Paris, FranceMuséum national d’Histoire naturelleParisFrance
Corresponding author: Eric Ythier (eythier@syntechresearch.com)
Academic editor: P. Stoev
20171212201772145632E37FFB9-2571-FFC5-FFA7-FFC34F5FFFB31300B527-8A50-41E3-8D5E-1C745846BBDF11501140910201721112017Eric Ythier, Wilson R. LourençoThis 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.http://zoobank.org/1300B527-8A50-41E3-8D5E-1C745846BBDF
Three new species of scorpions belonging to the genus Teuthraustes Simon, 1878 (Scorpiones: Chactidae) are described from the Amazonian and Pacific regions of Ecuador. The new descriptions raise to four the number of Teuthraustes species in Ecuadorian Amazonia and raise to two the number of species described from the Pacific region. The total number of species of Teuthraustes is now 27, including 15 in Ecuador. The geographical distribution of the genus in Ecuador is enlarged and its pattern of distribution in the country is also commented upon.
Ythier E, Lourenço WR (2017) The geographical patterns of distribution of the genus Teuthraustes Simon, 1878 in Ecuador and description of three new species (Scorpiones, Chactidae). ZooKeys 721: 45–63. https://doi.org/10.3897/zookeys.721.21529
Introduction
The genus Teuthraustes was created by Simon (1878) based on a new species, Teuthraustesatramentarius Simon, 1878 collected in Ecuador by M. Deville of the Brussels Museum. Both the genus and species descriptions are extremely reduced and poorly diagnosed. Between Simon’s (1878) description and the revision of the genus by Kraepelin (1911), thirteen additional species were described or transferred to Teuthraustes. With the exceptions of T.amazonicus (Simon, 1880) and T.glaber Kraepelin, 1912, both described from Peru, all other species are known from Ecuador. Even if the taxonomic status of some Ecuadorian species is still uncertain, this remarkable concentration of species in Ecuador is realistic and can be explained by biogeographic models (Lourenço 1995a).
From the revision by Kraepelin (1911) until the monograph work of Mello-Leitão (1945) no new species of this genus were described. Subsequently, five new species were described from Venezuela, T.carmelinae Scorza, 1954, T.adrianae González-Sponga, 1975, T.akananensis González-Sponga, 1984, T.maturaca González-Sponga, 1991 and T.reticulatus González-Sponga, 1991, three from Brazil, T.lisei Lourenço, 1994, T.braziliensis Lourenço & Duhem, 2010 and T.newaribe Lourenço, Giupponi & Pedroso, 2011, one from Colombia, T.guerdouxi Lourenço, 1995 and one from Peru, T.castiglii Rossi, 2015 (Lourenço 1994a, 1995b, Lourenço and Duhem 2010, Lourenço et al. 2011, González-Sponga 1996, Rossi 2015). Almost all the species of Teuthraustes, so far described, were collected in the Andean mountains in Ecuador and Colombia, and in the Amazonian highlands of Venezuela and Brazil. These highlands are known as the ‘Tepuys’. Exceptions remain however: T.amazonicus Simon, described from the region of Pebas, located on the banks of the Solimões River in Peruvian Amazonia, then later found in Brazilian and Colombian Amazonia, T.glaber Kraepelin and T.castiglii Rossi, both also described from the region of Pebas, Peru (to notice that the precise locality of T.glaber was originally indicated as only Peru, however in the personal notes by Simon the type specimen is indicated as from the region of Pebas), T.braziliensis Lourenço & Duhem, described from Brazilian Amazonia, T.dubius Borelli and T.festae Borelli, described from Morona-Santiago Province in Ecuador, T.rosenbergi Pocock, described from Guayas Province in Ecuador, and finally the three new species described in the present paper. In a recent publication by Brito and Borges (2015), an attempted checklist of the scorpions from Ecuador was proposed. This contribution is a compilation of previous works and no new species or locations were added neither to this fauna in general nor to the genus Teuthraustes in particular.
In the present paper, three new species of Teuthraustes are described from the lowlands of Ecuador: two from the Amazon region (Orellana and Sucumbíos Provinces; raising to four the number of Teuthraustes species in Ecuadorian Amazonia) and one from the rainforests of the Pacific Coast in Esmeraldas Province, this last species being the second record of a Teuthraustes species from the Pacific coastal region. The patterns of distribution presented by the species of the genus Teuthraustes in Ecuador are also discussed. This group remains, however, typical of highland formations of South America.
Geographical pattern of distribution of the genus Teuthraustes
The known geographical distribution of the genus Teuthraustes clearly indicates its endemic and disrupted nature. Of the 27 species known at present, nine are distributed in the Andean highlands of Ecuador. Another group of seven species has been described even more recently from a different highland site located between Brazil and Venezuela. This area clearly corresponds with the Imeri endemic centre which has been defined both for plants and for animals (Lourenço 2001, Prance 1982a, b). It is located in the ‘Tepuys’ region which lies mainly in Guayana, a floristic province that has been delineated botanically (Mori 1991). One species is known from the highlands of Colombia, 8 species are known from the lowlands of the Ecuadorian, Peruvian, Colombian and Brazilian Amazonia and 2 species are known from the Pacific coast region of Ecuador.
This outstanding concentration of Teuthraustes species in the Andean highlands and in the Imeri endemic centre may be similar to the ‘explosive’ pattern of speciation proposed by Gentry (1992) for plants of the genus Gasteranthus. According to Gentry (1992), it is probable that an entirely different evolutionary mode may be operating in these areas. The exceedingly dynamic speciation is perhaps mediated more by genetic transilience associated with genetic drift in small founder populations in a kaleidoscopically changing milieu, than by fine-tuned selection of the type generally suggested to be typical of lowland rain forest.
Several botanists (Gentry 1988, 1992) and entomologists (Erwin 1982, Wilson 1988) agree that tropical rainforests are the most species-rich ecosystems on earth. They also agree, on the basis of solid evidence, that the ‘epicentre’ of global biodiversity occurs in the tropical Andes, a region of the upper Amazonia which includes the North of Peru, Ecuador and the southern half of Colombia. This suggestion seems to be valid for plants, vertebrates and butterflies (Prance 1982a, b, Gentry 1992, Erwin 1982, Wilson 1988). The region is also one of the world’s greatest sites of alpha-diversity on scorpions (Lourenço 1994b). Consequently, the very high concentration of Teuthraustes species in the Andean region could perhaps be no more than the consequence of the great ecological diversity there.
Topographic map of Ecuador showing the distribution of the known species of Teuthraustes.
https://binary.pensoft.net/fig/173357
It is obvious that scorpion speciation and differentiation is by no means recent. As stated by Haffer (1982), the isolation of large populations due to Tertiary palaeogeographic changes undoubtedly played a major role in establishing the basic distributional and evolutionary patterns of the tropical floras and faunas at higher taxonomic levels of family and genera. At the same time, members of less ‘plastic’ groups with low evolutionary rates in the present flora and fauna survived relatively unchanged since Tertiary times. Since the Andes arose in the form of strings of growing islands from a marine geosynclinal basin, there was no pre-Andean continuous and widespread lowland fauna occupying what was later to become the Andes and their forelands. Consequently, Andean elements must have come from abroad. The ‘Tepuys’ region which includes the Imeri endemic centre, is located in the Precambrian Guiana Craton (or shield). From a geological point of view the ‘Tepuys’ are composed of sheer blocks of Precambrian sandstone and quartzite rocks. These ‘mesas’ are the remains of a huge sandstone plateau that once covered the granite basement complex between what is today the northern border of the Amazon Basin and the Orinoco, between the Atlantic coast and the Rio Negro (Lourenço and Duhem 2009).
Ecological, paleoclimatic, and palynologic data (Prance 1982b) indicate that the apparent ‘stability’ of present-day rainforests was interrupted by periods of climatic change through several dry/wet/dry episodes of the late Cenozoic period, and especially during more recent Pleistocene and Holocene epochs. During the earlier Quaternary period, temperate regions were glaciated. Cooler and drier conditions prevailed in the present tropical zones and reduced the rainforest to savannas or dry-forests except in localized regions where conditions of temperature and humidity allowed them to persist. During these glacial phases, more mesic species of scorpions, such as those of the genus Teuthraustes, and also of other mesic genera such as Chactas Gervais, 1844 and Vachoniochactas González-Sponga, 1978 probably experienced a more enlarged range of distribution than that observed today. With the return of the present interglacial phase these genera are again restricted to the highlands where mesic conditions prevail. Some species of the genera Teuthraustes and Chactas, however, probably evolved in and became adapted to the tropical forest when this one expanded and coalesced throughout the entire Neotropical lowlands (Lourenço 1995a, Lourenço et al. 2005). Consequently, one can expect new species of both genera still to be found in the lowlands of Amazonia.
Vegetation map of Ecuador showing the distribution of the known species of Teuthraustes.
https://binary.pensoft.net/fig/173359Methods
Measurements and illustrations were made using a Wild M5 stereo-microscope with a drawing tube (camera lucida) and an ocular micrometre. Measurements follow those of Stahnke (1970) and are given in mm. Trichobothrial notations are those developed by Vachon (1974) and the morphological terminology mostly follows that of Hjelle (1990).
Taxonomic treatmentFamily Chactidae Pocock, 1893Genus Teuthraustes Simon, 1878Composition of the genus Teuthraustes
Ecuador, Orellana Province (formerly Napo), Santa Maria de Huiririma 0°43'0"S, 75°37'0"W) VI/1976 (British expedition and local people), rainforest, under log. Pre-adult female holotype. Type material deposited in the Muséum national d’Histoire naturelle, Paris, France.
Etymology.
The specific name honours Dr. Khosro Khodayari, founder, President and CEO of SynTech Research, Davis, California, USA, in recognition of his support for the study of scorpions.
Diagnosis.
Moderate to small scorpion with 35.1 mm in total length. Colouration reddish brown to dark brown. Body and appendages very intensely granulated with a rather thin granulation. Pectines with 6–6 teeth in female. Fixed and movable fingers of chela with 5–5 rows of granules; extremities of fingers with 3 granules. Ventral carinae present on metasomal segments I to IV, but weak on I. Trichobothrial pattern of type C neobothriotaxic ‘majorante’.
Description.
Based on female holotype.
Colouration.
General colouration basically reddish brown to dark brown. Prosoma: carapace reddish brown with a few paler spots; eyes blackish. Mesosoma: tergites reddish brown, with VII slightly paler with some yellow spots; venter and sternites reddish yellow; pectines and genital operculum with the same colour as sternites. Metasoma: segments reddish brown, with darker zones over carinae; vesicle reddish yellow with the tip of the aculeus dark red. Chelicerae: reddish yellow, with some diffuse variegated brown spots; fingers dark red with teeth reddish yellow. Pedipalps: dark brown with blackish carinae; cutting edges of fingers reddish. Legs: reddish yellow to reddish brown without spots.
Morphology.
Prosoma: carapace intensely granulated, with a dense and thin granulation; furrows shallow; sternum pentagonal, wider than long. Mesosoma: tergites almost acarinate, with a thin and dense granulation; sternites smooth and shiny, only VII with a few granulations; spiracles oval to rounded-shaped and conspicuous; pectinal tooth count 6–6, fulcra vestigial. Metasoma: segments I to III wider than long; metasomal tegument on segments I to IV with conspicuous granulations; segment V with spinoid granulations ventrally; carinae on segments I–V strongly developed; ventral present on all segments, less marked on I; telson with strongly marked granulations, only dorsal face smooth; aculeus shorter than vesicle. Chelicerae: dentition typical of the family Chactidae (Vachon 1963), and with dense setation ventrally and internally. Pedipalps: femur with dorsal internal, dorsal external and ventral internal carinae strongly marked; ventral external carina absent; dorsal, ventral and internal aspects with granulations; patella granulated with moderate carinae; chela very strongly granulated; internal aspect with conspicuous granules; dentate margins on movable and fixed fingers with 5–5 rows of granules; distal edge of fingers with three granules; trichobothriotaxy of type C; neobothriotaxic ‘majorante’ (Vachon 1974). Legs: tarsi with short setae disposed in a single line.
The species can be distinguished from the others congeners in particular from Teuthraustesatramentarius Simon, which is also distributed in Ecuador, but exclusively in the high central Andes, by the following features: (i) a thin but very intense granulation over body and appendages, particularly marked on legs (ii) ocular tubercle much less pronounced, (iii) pectines are wider, (iv) pedipalpal chela are not bulk and elongated, (v) metasomal segments I to III wider than long.
Teuthrausteskhodayarii sp. n. Female holotype. A Chelicera, dorsal aspect B Disposition of the granulation over the dentate margins of pedipalp-chela movable finger C–H Trichobothrial pattern C–D Chela, dorso-external and ventral aspects E Femur, dorsal aspect F–H Patella, dorsal F external G and ventral H aspects. Scale bars 1 mm.v
https://binary.pensoft.net/fig/173363
Morphometric values (in mm) of female holotypes of T.khodayarii sp. n., T.giupponii sp. n., T.kuryi sp. n., and T.atramentarius Simon, 1878.
Ecuador, Sucumbíos Province (formerly Napo), Dureno/Cuyabeno, near lake Cuyabeno, Cuyabeno Wildlife Reserve (0°07'00"S, 75°50'00"W) VI/1976 (British expedition and local people), rain-forest, under stone. Female holotype. Type material deposited in the Muséum national d’Histoire naturelle, Paris, France.
Etymology.
The specific name honours Dr. Alessandro Ponce de Leão Giupponi, Fundação Oswaldo Cruz, Rio de Janeiro, for his contributions to the study of scorpions.
Diagnosis.
Moderate scorpions with 52.1 mm in total length. Colouration reddish to reddish yellow. Body and appendages weakly granulated, with minute punctation. Pectines small with 6–6 teeth in female. Fixed and movable fingers of chela with 5–5 rows of granules. Ventral carinae present on metasomal segments I to IV but inconspicuous on I. Trichobothrial pattern of type C neobothriotaxic ‘majorante’.
Description.
Based on female holotype.
Colouration.
General colouration basically reddish to reddish yellow. Prosoma: carapace reddish; eyes blackish. Mesosoma: tergites reddish yellow, paler than carapace, with confluent yellowish strips; venter and sternites reddish yellow to yellow; pectines, genital operculum, and sternites yellow. Metasoma: segments reddish, with darker zones over carinae; vesicle reddish yellow with the tip of the aculeus dark red. Chelicerae: yellow, with some diffuse variegated reddish spots at the base of fingers; fingers reddish yellow; teeth reddish. Pedipalps: dark reddish; carinae blackish. Legs: reddish yellow with pale spots.
Morphology.
Prosoma: carapace acarinate, with dense minute granulations; lateral edges smooth; furrows shallow; sternum pentagonal, wider than long. Mesosoma: tergites acarinate, with a few granulations and some punctations; sternites, smooth and shiny; spiracles oval to rounded-shaped and conspicuous; VII acarinate with a few granules; pectinal tooth count 6–6, fulcra inconspicuous. Metasoma: segments I and II wider than long; metasomal tegument on segments I to IV with strong granulations; segment V with some spinoid granulations ventrally; carinae on segments I–V strongly developed; ventral present on segments I to IV; telson with a few ventral granulations, other faces almost smooth; aculeus shorter than vesicle. Chelicerae: dentition typical of the family Chactidae (Vachon 1963), and with dense setation ventrally and internally. Pedipalps: femur with dorsal internal, dorsal external and ventral internal carinae strongly marked; ventral external carina represented by a few granules; dorsal, ventral and internal aspects with thin granulations; patella smooth with weak carinae; chela smooth and almost acarinate; internal aspect with a few small granules; dentate margins on movable and fixed fingers with 5–5 rows of granules; trichobothriotaxy of type C; neobothriotaxic ‘majorante’ (Vachon 1974). Legs: tarsi with short setae disposed in a single line.
The new species can be distinguished from other the congeners in particular from Teuthraustesoculatus Pocock, which is also distributed in Ecuador, but in the high central Andes, by the following features: (i) paler general colouration, reddish to reddish yellow, (ii) tergites and pedipalps weakly granulate to smooth, (iii) carapace with some thin granulations (iv) lateral eyes small and apart from each other, (v) anterior edge of carapace not straight, lobate, (vi) ventral carinae on metasomal segment I inconspicuous.
Teuthraustesgiupponii sp. n. Female holotype. A Chelicera, dorsal aspect B–G Trichobothrial pattern B–C Chela, dorso-external and ventral aspects D Femur, dorsal aspect E–G Patella, dorsal E external F and ventral G aspects. Scale bars 1 mm.
Ecuador, Esmeraldas Province (N00.88883, W078.53732), 873 m, in zone where rainforest was recently destroyed, under log, 17/III/2011 (A. Chagas, A. Giupponi, A. Kury, M. Vega). Female holotype and female paratype. Holotype deposited in the Museo de Zoologia, Pontificia Universidad Católica de Quito, Ecuador; paratype deposited in the Museu Nacional, Rio de Janeiro, Brazil.
Etymology.
Specific name honours Prof. Adriano B. Kury, Museu Nacional, Universidade Federal do Rio de Janeiro, Brazil, for his important contribution to the study of arachnids.
Diagnosis.
Moderate to large scorpions with 60–61 mm in total length. Colouration dark brown to blackish. Body and appendages strongly granulated. Pectines with 7–7 teeth in females. Pedipalps bulk with short fingers; fixed and movable fingers of chela with 5–6 rows of granules. Metasoma long and strong; ventral carinae strongly marked on metasomal segments I to IV. Trichobothrial pattern of type C neobothriotaxic ‘majorante’.
Description.
Based on female holotype and female paratype.
Colouration.
General colouration basically dark brown to blackish. Prosoma: carapace dark brown; eyes blackish. Mesosoma: tergites reddish brown to dark brown, slightly paler than carapace; venter and sternites reddish brown to dark brown; pectines and genital operculum yellow. Metasoma: segments blackish brown, with darker zones over carinae; vesicle reddish brown with the base of the aculeus reddish yellow. Chelicerae: reddish yellow, with some diffuse variegated reddish spots at the base of the fingers; fingers dark reddish. Pedipalps dark brown to blackish; carinae blackish. Legs dark brown to blackish.
Morphology.
Prosoma: carapace almost acarinate, but with dense strongly marked granulations on the entire surface, except on the zone of furrows; furrows deep; sternum pentagonal, wider than long. Mesosoma: tergites intensely granulated but less marked than carapace; sternites, smooth and shiny; spiracles oval-shaped and conspicuous; VII acarinate with granulations; pectinal tooth count 7–7 in both females, holotype and paratype, fulcra vestigial. Metasoma: segments I and II wider than long; metasomal tegument on segments I to IV strongly granulated including dorsal aspect; segment V with some spinoid granulations ventrally; carinae on segments I–V strongly developed; ventral present on all segments; telson strongly granulated; aculeus shorter than vesicle. Chelicerae: dentition typical of the family Chactidae (Vachon 1963), and with dense setation ventrally and internally. Pedipalps: femur with dorsal internal, dorsal external and ventral internal carinae strongly marked; ventral external carina vestigial; dorsal, ventral and internal aspects granulated; patella granulated with well-marked carinae; chela strongly granulated and with most carinae well-marked; dentate margins on movable and fixed fingers with 5–6 rows of granules; trichobothriotaxy of type C; neobothriotaxic ‘majorante’ (Vachon 1974). Legs: tarsi with short setae disposed in a single line.
The new species can be distinguished from the others congeners in particular from Teuthraustesatramentarius Simon, which is also distributed in Ecuador, but exclusively in the high central Andes, by the following features: (i) carapace, tergites, pedipalps, metasoma, and telson strongly granulated, (ii) metasomal segments I to V long and strong with well-marked ventral carinae, (iii) pedipalps bulk with short fingers on chela, (iv) ventral aspect with a darker pigmentation, reddish brown to dark brown.
Teuthrausteskuryi sp. n. Female holotype. A Chelicera, dorsal aspect B Disposition of the granulation over the dentate margins of pedipalp-chela movable finger C–H Trichobothrial pattern C–D Chela, dorso-external and ventral aspects E Femur, dorsal aspect F–H Patella, dorsal F external G and ventral H aspects. Scale bars 1 mm.
The female holotype of Teuthraustesatramentarius was studied and its morphometric values (in mm) are presented in Table 1. The holotype is deposited in the Muséum national d’Histoire naturelle, Paris under the N° RS-0763 (Simon’s N° 3019). In the catalogue of the scorpions of the World (Sissom 2000) the holotype is cited as deposited in the “Musée Royal d’Histoire naturelle de Belgique” in Brussels. This is, however, incorrect.
Amazon region, Ecuador. Natural habitat of Teuthrausteskhodayarii sp. n. and Teuthraustesgiupponii sp. n. (photograph C. Benros-Ythier; E. Ythier in the photo).
We are most grateful to Adriano Kury (Museu Nacional, Rio de Janeiro, Brazil) and Alessandro Giupponi (Fundação Oswaldo Cruz, Rio de Janeiro, Brazil) for the loan of part of the studied material and for the information and photos from their field work. We are also grateful to two anonymous referees and linguistic editor for useful comments and suggestions, as well as to Elise-Anne Leguin (MNHN, Paris, France) for her support with the preparation of the photos.
ReferencesBorelliA (1899) Viaggio del Dr. Enrico Festa nell’Ecuador e regioni vicine. XVIII: Scorpioni. Bollettino del Museo di Zoologia ed Anatomia comparata della Regia Università di Torino 189, 14(345): 1–18.Botero-TrujilloRFlórez-DazaE (2006) First Report of Teuthraustesamazonicus (Simon, 1880) (Scorpiones: Chactidae) in Colombia.13: 187–188.BritoGBorgesA (2015) A checklist of the scorpions of Ecuador (Arachnida: Scorpiones), with notes on the distribution and medical significance of some species. Journal of venomous animals and toxins including tropical diseases 21: 23. https://doi.org/10.1186/s40409-015-0023-xErwinTL (1982) Tropical forests: Their richness in Coleoptera and other Arthropod species.36: 74–75.GentryAH (1988) Tree species richness of upper Amazonian forests.85: 156–159. https://doi.org/10.1073/pnas.85.1.156GentryAH (1992) Tropical forest biodiversity: distributional patterns and their conservational significance.63: 19–28. https://doi.org/10.2307/3545512González-SpongaMA (1975) Teuthraustesadrianae (Scorpionida: Chactidae). Nueva especie en el tepui “La Neblina”, Territorio Federal Amazonas, Venezuela.8: 1–20.González-SpongaMA (1984) Tres nuevas especies de la Amazonia de Venezuela. (Scorpionida: Chactidae).44(135–136): 142–165.González-SpongaMA (1991) Arácnidos de Venezuela. Escorpiones del Tepui “La Neblina”, Territorio Federal Amazonas. (Scorpionida: Chactidae: Butidae).50(163–164): 11–62.González-SpongaMA (1996) Cuadernos Lagoven, Caracas, 204 pp.HafferJ (1982) General aspects of the refuge theory. In: PranceGT (Ed.) Biological Diversification in the Tropics., 6–24.HjelleJT (1990) Anatomy and morphology. In: PolisGA (Ed.) The Biology of Scorpions., 9–63.KraepelinK (1896) Neue und weniger bekannte skorpione. Mitt Naturhist Mus, Beiheft zum Jahrb Hamb Wiss Anst. 1896, 13: 119–46.KraepelinK (1912) Neue Beiträge zur Systematik der Gliederspinnen. II. Chactinae (Scorpiones). Mitteilungen aus dem Naturhistorischen Museum (2. Beiheft zum Jahrbuch der Hamburgischen wissenschaftlichen Anstalten, 1911) 29: 43–88.LourençoWR (1994a) Scorpion biogeographic patterns as evidence for a Neblina-São Gabriel endemic center in Brazilian Amazonia.19: 181–185.LourençoWR (1994b) Diversity and endemism in tropical versus temperate scorpion communities.70: 155–160.LourençoWR (1995a) Les scorpions (Chelicerata, Scorpiones) de l’Équateur avec quelques considérations sur la biogéographie et la diversité des espèces. Revue suisse de zoologie 102: 61–88. https://doi.org/10.5962/bhl.part.80459LourençoWR (1995b) Considérations sur la biogéographie des espèces appartenant au genre Teuthraustes Simon, 1878 (Chelicerata, Scorpiones, Chactidae).101: 201–206.LourençoWR (2001) Scorpion diversity in Tropical South America: Implications for conservation programs. In: BrownellPPolisGA (Eds) Scorpion biology and research., 406–416.LourençoWRAguiarNOFranklinE (2005) First record of the scorpion genus Chactas Gervais, 1844, for Brazil with description of a new species from western State of Amazonas (Scorpiones: Chactidae).984: 1–8. https://doi.org/10.11646/zootaxa.984.1.1LourençoWRDuhemB (2009) The genus Vachoniochactas Gonzalez-Sponga (Scorpiones, Chactidae), a model of relictual distribution in past refugia of the Guayana region of South America.332: 1085–1091. https://doi.org/10.1016/j.crvi.2009.09.006LourençoWRDuhemB (2010) The geographical pattern of distribution of the genus Teuthraustes Simon (Scorpiones, Chactidae) in South America and description of a new species.333: 858–863. https://doi.org/10.1016/j.crvi.2010.09.005LourençoWRGiupponiAPLPedrosoDR (2011) New species of Chactidae (Scorpiones) from the upper Rio Negro in Brazilian Amazonia.49: 65–73.Mello-LeitãoC (1939) Una nueva especie de alacrán del género Chactas.17: 147–148.Mello-LeitãoC (1945) Escorpiões sul-americanos.40: 7–468.MoriSA (1991) The Guayana lowland floristic Province.67: 67–75.OchoaJAPintoda Rocha R (2012) On the taxonomic status of Chactascamposi Mello-Leitão, 1939 (Scorpiones, Chactidae).3210: 61–68.PranceGT (1982a) Forest refuges: evidence from woody angiosperms. In: PranceGT (Ed.) Biological Diversification in the Tropics., 137–158.PranceGT (1982b) Columbia University Press, New York, 714 pp.PocockRI (1893) A contribution to the study of neotropical scorpions.6(68): 77–103. https://doi.org/10.1080/00222939308677589PocockRI (1898) Descriptions of some new scorpions from Ecuador. Annals and Magazine of Natural History Sér 7, 6(1): 413–22.PocockRI (1900) Some new or little-known Neotropical scorpions in the British Museum. Annals and Magazine of Natural History Sér 7, (5): 469–78. https://doi.org/10.1080/00222930008678315Rojas-RunjaicFJMDe SousaL (2007) Catálogo de los escorpiones de Venezuela (Arachnida: Scoripones). Boletín Sociedad Entomológica Aragonesa, n1 40(2007): 281–307.RossiA (2015) Il genere Teuthraustes Simon, 1878 in Perù, con la descrizione di una nuova specie (Scorpiones: Chactidae). Rivista Aracnologica Italiana, 5, Supplemento: 21–27.ScorzaJV (1954) Contribución al estudio de los alacranes venezolanos. Clave para la identificación de especies y consideraciones genrales sobre los escorpiones domiciliarios.2(2): 157–165.SimonE (1878) Etudes arachnologiques. 9e Mémoire. XV. Descriptions de deux nouveaux genres de l’ordre des Scorpiones.8: 399–400.SimonE (1880) Etudes Arachnologiques.12ème mémoire. XVIII. Descriptions de genres et espèces de l’ordre des scorpions. Annales de la Société Entomologique de France ser. 5, (10): 377–398.SissomWD (2000) Family Chactidae Pocock, 1893. In: FetVSissomWDLoweGBraunwalderME (Eds) Catalog of the scorpions of the World., 287–322.StahnkeHL (1970) Scorpion nomenclature and mensuration.81: 297–316.VachonM (1963) De l’utilité, en systématique, d’une nomenclature des dents des chélicères chez les Scorpions.35: 161–166.VachonM (1974) Etude des caractères utilisés pour classer les familles et les genres de Scorpions (Arachnides). 1. La trichobothriotaxie en arachnologie. Sigles trichobothriaux et types de trichobothriotaxie chez les Scorpions.140: 857–958.WilsonEO (1988) The current state of biological diversity. In: WilsonEO (Ed.) Biodiversity., 3–18.