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A checklist of the scorpions of Ecuador (Arachnida: Scorpiones), with notes on the distribution and medical significance of some species


Ecuador harbors one of the most diverse Neotropical scorpion faunas, hereby updated to 47 species contained within eight genera and five families, which inhabits the “Costa” (n = 17), “Sierra” (n = 34), “Oriente” (n = 16) and “Insular” (n = 2) biogeographical regions, corresponding to the western coastal, Andean, Amazonian, and the Galápagos archipelago regions, respectively. The genus Tityus Koch, in the family Buthidae, responsible for severe/fatal accidents elsewhere in northern South America and the Amazonia, is represented in Ecuador by 16 species, including T. asthenes, which has caused fatalities in Colombia and Panama, and now in the Ecuadorian provinces of Morona Santiago and Sucumbíos. Underestimation of the medical significance of scorpion envenoming in Ecuador arises from the fact that Centruroides margaritatus (Gervais) (family Buthidae) and Teuthraustes atramentarius Simon (family Chactidae), whose venoms show low toxicity towards vertebrates, frequently envenom humans in the highly populated Guayas and Pichincha provinces. This work also updates the local scorpion faunal endemicity (74.5 %) and its geographical distribution, and reviews available medical/biochemical information on each species in the light of the increasing problem of scorpionism in the country. A proposal is hereby put forward to classify the Ecuadorian scorpions based on their potential medical importance.


Ecuador, despite its small size (only 250,000 km2 or 1.5 % of South America), ranks 17th among the nations of the world in biodiversity [1, 2]. This is attributable to, among other factors, the confluence of several biogeographic regions: Chocó and Tumbez (encompassing the “Costa” region), northern and south-central Andes (Sierra” region), the northern and southwestern Amazon (Oriente” region) and the insular region of Galápagos (Fig. 2). Ecuador harbors one of the richest arachnid faunas of the Neotropics [3]; specifically, its scorpion fauna ranks high amongst South American countries in terms of diversity, with 12.70 species per 100,000 km2 [4].

Pioneering work by Eugéne Simon, Reginald I. Pocock, Alfredo Borelli, Karl Kraepelin, and Cândido de Mello-Leitão initiated the cataloguing of Ecuadorian scorpions [513]. Although less known, the work of the Ecuadorian taxonomist Francisco Campos [14, 15], together with Behr-Castillo and Correa [16], also contributed to the knowledge of local scorpions, particularly in the province of Guayas. The work of Wilson R. Lourenço has allowed recognition of Ecuador as part of a region exhibiting the highest alpha-diversity for scorpions in the world, also encompassing Southern Colombia, the Northeast region of Peru, and the Upper Amazon region of Brazil [17].

Particularly, the genera Tityus C. L. Koch (in the family Buthidae) and Teuthraustes Simon (in the family Chactidae) show a high concentration of species in Ecuador [18, 19]. A center of endemism in Ecuador for Teuthraustes has been proposed based on its extreme local diversity [20]. Despite such diversity, little is known about the toxicity of local scorpions, particularly within the speciose genus Tityus, which contains all medically important species in South America, and exhibits a phylogenetic divergence paralleled by functional, structural, and immunological differences among their toxins [21, 22].

Mostly dating from records obtained at the turn of the 19th century and from the 1900–1920 period, type localities for a number of Ecuadorian species are obscure. An example of this situation shown recently is the chactid Chactas rubrolineatus Simon, described by Eugène Simon from Rio Içá in 1880, which was wrongly assigned to Ecuador by Mello-Leitão [10] when in fact its location lies in Brazil [23].

The goal of this work is therefore to update the list of species and review the literature on scorpion Ecuadorian fauna from geographical and toxicological standpoints whenever the information is available. This idea arises, on one hand, from the increasing clinical relevance of some species in the country, with several fatal and severe infant cases reported from the provinces of Sucumbíos and Morona Santiago in 2012–2014 ([24]; Dr. Jorge Blanco, Fundación Herpetológica Gustavo Orcés, personal communication). Comprehension of the basis underlying the extreme diversity of the Ecuadorian scorpion fauna, particularly in the case of those species toxic to humans, necessarily relies on the correct assignment of collection localities.

Here follows a list of the taxa currently recognized to inhabit Ecuador, including comments on their distribution and type localities, after confronting published collection sites with contemporary geographical names. We used various search engines for placing type localities (Google Earth, GeoNames). Taxa are organized in alphabetical order. Figure 1 summarizes the occurrence of individual species per province; the map in Fig. 2 identifies provinces in the contemporary political map of Ecuador. Information on the location of holotypes and syntypes for Ecuadorian species is available from the cited literature [17, 2532]. We also review the potential medical importance of scorpion genera and species prevalent in Ecuador.

Fig. 1
figure 1

Distribution of scorpion species per political province and biogeographical area in Ecuador. Collection localities not yet defined are marked with question marks

Fig. 2
figure 2

Political provinces of Ecuador and biogeographical regions encompassing such provinces. “Costa” region: (1) Esmeraldas, (2) Manabí, (3) Los Ríos, (4) Guayas, (5) Santa Elena, (6) El Oro. “Sierra” region: (7) Carchi, (8) Imbabura, (9) Pichincha, (10) Santo Domingo de los Tsáchilas, (11) Cotopaxi, (12) Tungurahua, (13) Bolívar, (14) Chimborazo, (15) Cañar, (16) Azuay, (17) Loja. “Oriente” región: (18) Sucumbíos, (19) Napo, (20) Francisco de Orellana, (21) Pastaza, (22) Morona Santiago, (23) Zamora Chinchipe. “Insular” region: Galálapagos islands

Annotated list of Ecuadorian scorpion species

  • Family Bothriuridae Simon, 1880

    • Genus Brachistosternus Pocock, 1893

      • Brachistosternus (Brachistosternus) pegnai Cekalovic, 1969

      • Brachistosternus (Brachistosternus) ehrenbergii (Gervais, 1841)

  • Family Buthidae Simon, 1880

  • Genus Ananteris Thorell, 1891

    • Ananteris ashmolei Lourenço, 1981

    • Ananteris festae Borelli, 1899

    • Ananteris mariaelenae Lourenço, 1999

  • Genus Centruroides Marx, 1889

    • Centruroides exsul (Meise, 1933)

    • Centruroides gracilis (Latreille, 1804)

    • Centruroides margaritatus (Gervais, 1841)

  • Genus Tityus C. L. Koch, 1836

    • Tityus (Atreus) asthenes Pocock, 1893

    • Tityus (Archaeotityus) bastosi Lourenço, 1984

    • Tityus (Atreus) crassicauda Lourenço & Ythier, 2013

    • Tityus (Tityus) demangei Lourenço, 1981

    • Tityus (Tityus) ecuadorensis Kraepelin, 1896

    • Tityus (Atreus) forcipula (Gervais, 1844)

    • Tityus (Tityus) gasci Lourenço, 1981

    • Tityus (Archaeotityus) intermedius Borelli, 1899

    • Tityus (Archaeotityus) julianae Lourenco, 2005

    • Tityus (Tityus) jussarae Lourenço, 1988

    • Tityus (Atreus) pugilator Pocock, 1898

    • Tityus (Tityus) roigi Maury & Lourenço, 1987

    • Tityus (Tityus) simonsi Pocock, 1900

    • Tityus (Archaeotityus) silvestris Pocock, 1897

    • Tityus (Atreus) timendus Pocock, 1898

    • Tityus (Atreus) ythieri Lourenço, 2007

  • Family Caraboctonidae Kraepelin, 1905

  • Genus Hadruroides Pocock, 1893

    • Hadruroides (Hadruroides) charcasus (Karsch, 1879)

    • Hadruroides (Lourencoides) doriai Rossi, 2014

    • Hadruroides (Lourencoides) elenae Rossi, 2014

    • Hadruroides (Lourencoides) galapagoensis Maury, 1974

    • Hadruroides (Lourencoides) maculatus (Thorell, 1876)

    • Hadruroides (Lourencoides) moreti Rossi, 2014

    • Hadruroides (Lourencoides) udvardyi Lourenço, 1995

  • Family Chactidae Laurie, 1896

  • Genus Chactas Gervais, 1844

    • Chactas mahnerti Lourenço, 1995

    • Chactas moreti Lourenço, 2014

    • Chactas yaupi Lourenço, 2014

  • Genus Teuthraustes Simon, 1878

    • Teuthraustes atramentarius Simon, 1878

    • Teuthraustes camposi (Mello-Leitão, 1939)

    • Teuthraustes dubius (Borelli, 1899)

    • Teuthraustes festae (Borelli, 1899)

    • Teuthraustes gervaisii (Pocock, 1893)

    • Teuthraustes lojanus (Pocock, 1900)

    • Teuthraustes oculatus Pocock, 1900

    • Teuthraustes ohausi Kraepelin, 1912

    • Teuthraustes rosenbergi (Pocock, 1898)

    • Teuthraustes simonsi (Pocock, 1900)

    • Teuthraustes whymperi (Pocock, 1893)

    • Teuthraustes wittii (Kraepelin, 1896)

  • Family Troglotayosicidae Lourenço, 1998

  • Genus Troglotayosicus Lourenço, 1981

    • Troglotayosicus vachoni Lourenço, 1981

Family Bothriuridae

Genus Brachistosternus

This genus is amply distributed in the coastal region of Peru and northern Chile, and comprises 41 species contained within two subgenera, Brachistosternus Pocock and Ministernus Francke [33]. Records for Ecuador include only two species, Brachistosternus (Brachistosternus) pegnai Cekalovic, from the province of Carchi, and Brachistosternus (Brachistosternus) ehrenbergii (Gervais), whose current distribution in the country is not known. Although the sting by some species, including B. (B.) ehrenbergii, can be painful to humans, there are no reports of fatal envenoming by taxa in this genus. In Peru, B. (B.) ehrenbergii is a highly abundant synanthropic scorpion along the coastline [34].

A 6.7 kDa toxin denominated Be1 has been isolated from the venom of B. (B.) ehrenbergii which produces salivary secretion and spastic paralysis in mice at a dose of 3 mg/kg upon intraperitoneal injection and is lethal after two hours [35]. Be1 only comprises 7 % (w/w) of the total venom protein content, in comparison with the typical 20-30 % content of low-molecular-weight neurotoxins in the venom from Tityus species [36], which probably explains the low lethal dose in mice of B. (B.) ehrenbergii crude venom (subcutaneous injection), which is around 20 mg/kg [34]. According to its molecular mass and physiological effects, Be1 may belong to the sodium channel-active family of scorpion toxins (NaScTx).

It is not known whether other Brachistosternus spp., including those prevalent in Ecuador, are of equally low toxicity to mice, but their medical importance requires evaluation considering the higher sensitivity of humans (five-fold more susceptible than mice) to scorpion venom [37]. As venom of another bothriurid from Australia, Cercophonius squama (Gervais), contains only primitive homologs of NaScTxs (lipolytic-like peptides), South American representatives of the family Bothriuridae (including those inhabiting Ecuador) might have diverged toxinologically from those genera prevalent in Southeast Asia [38].

  1. 1.

    Brachistosternus (Brachistosternus) pegnai Cekalovic, 1969:163–168.

    This species is reported in San Gabriel, “Carcha,” which actually corresponds to the province of Carchi, northern Ecuador [39]. In his original description, Cekalovic [25] does not specify the province of origin but provided a map that places the type locality roughly within Carchi. San Gabriel is at an altitude of 2,980 m (0.59318 N, 77.83078 W), well above the arid and semi-arid habitats of species within this genus prevalent in central Peru and northern Chile but related to Andean congenerics from Argentina, Chile, Bolivia, and Peru [40]. B. (B.) pegnai type locality is at the northernmost limit of the genus distribution range [33].

  1. 2.

    Brachistosternus (Brachistosternus) ehrenbergii (Gervais, 1841:285).

    B. (B.) ehrenbergii has been reported as present in Ecuador [41], although Ochoa and Ojanguren Affilastro [42] have verified its presence only from northern Chile to central Peru. Lourenço [18] places B. (B.) ehrenbergii Ecuadorian populations in the province of Santa Elena without providing precise locations and thus the species has been assigned to this province (Fig. 1), pending new findings in Ecuador.

Family Buthidae

Genus Ananteris

This genus comprises one of the smallest Neotropical buthids, between 15 and 41 mm of total body length in the case of Ecuadorian species. They are clearly recognizable by their densely spotted pigmentation, elongated telson, and pectines without fulcra [41]. No venoms from this genus have ever been analyzed, although toxins from Ananteris spp. are predicted to be ancestral to toxins produced by Tityus spp. given the Gondwanian distribution of Ananteris, since extant species are found both in Africa and Central/South America [43].

  1. 1.

    Ananteris ashmolei Lourenço, 1981:644–648

    Collected from Cueva de los Tayos (“Cave of the Oilbirds”) (1.9333S, 77.7928 W), a natural cave located on the eastern slopes of the Andes, in the province of Morona Santiago [44].

  1. 2.

    Ananteris festae Borelli, 1899:1–4.

    Collected from Rio Peripa by Enrico Festa during his 1895–1898 trip to Ecuador [7]. Assigning a precise location to Festa’s site of collection is not possible since the provinces of Guayas, Manabí, Santo Domingo de los Tsáchilas, and Pichincha currently share this river. A. festae is reported from the provinces of Los Ríos (near Quevedo) and Pichincha, confirming its prevalence in the Inter-Andean valley region of Ecuador [19, 26, 45].

  1. 3.

    Ananteris mariaelenae Lourenço, 1999:97–99.

    Type material from 75–80 km northeast of Chone, northern section of the province of Manabí [26].

Genus Centruroides

This genus contains three species in Ecuador. Venom from Centruroides margaritatus Gervais, the most common scorpion in the coastal region of Ecuador, is richer in toxins active against potassium channels and also antimicrobial peptides in comparison with the higher content of sodium channel-active toxins typically found in venoms of toxic Centruroides species inhabiting Mexico and the southern United States [46, 47], explaining the lower toxicity of C. margaritatus to vertebrates.

  1. 1.

    Centruroides exsul (Meise, 1933:27).

    This species is endemic to the Galápagos islands, the type material having been collected at Floreana Island (1.1751S, 90.263 W) [48]. Distribution: Islands of Española, Fernandina, Floreana, Marchena, Pinta, San Cristóbal, San Salvador, Santa Cruz, and Santiago. This species seems to be confined to the low dry arid zone, except for Pinta where it is found in evergreen forests [49].

  1. 2.

    Centruroides gracilis (Latreille, 1804:127).

    Lourenço [18] reports this species roughly within the province of Santa Elena but no specific locations are provided. Identity of true Ecuadorian C. gracilis populations is pending since records of this species in South America have been questioned [50].

  1. 3.

    Centruroides margaritatus (Gervais, 1841:281–282).

    This species (Fig. 3) is by far the most abundant scorpion along the Ecuadorian coast and responsible for the majority of envenoming cases in the metropolitan area of Guayaquil, province of Guayas, the most populated city of Ecuador [14,16,]. It is a large species (65–100 mm), with carapace and tergites dark yellow-brown and metasomal segments I–IV yellow-brown, darker on IV; V and telson dark reddish brown [50].

    Fig. 3
    figure 3

    Distribution in Ecuador of synanthropic species Teuthraustes atramentarius Simon and Centruroides margaritatus (Gervais). Geographical ranges are taken from Fig. 1. C. margaritatus specimen is from Mapasingue County, Guayaquil (picture by Xavier Cornejo, Facultad de Ciencias Naturales, Universidad de Guayaquil). T. atramentarius specimen (collected in Quito, Pichincha Province) is from the collection of the Invertebrate Museum, Pontificia Universidad Católica del Ecuador (photograph by Tatiana Torres)

The type locality of this species is Isla Puná, at the entrance of the Gulf of Guayaquil, currently belonging to the province of Guayas [50]. This species has been reported from the coastal provinces of Los Ríos and Santa Elena, and the “Sierra” province of Loja (Fig. 1), but no data are available on its presence in the coastal provinces of Esmeraldas and El Oro [50]. The records for the “Sierra” provinces of Pichincha and Chimborazo date from 1901–1907 and have not been confirmed since [51]. This species has been the subject of controversy for more than a century in relation to its real range of distribution as has been frequently misidentified with its allied species, Centruroides gracilis (Latreille), and Centruroides edwardsii (Gervais). The matter was settled by Armas et al. [50] who differentiated C. margaritatus from its congeners based on its geographical distribution in South America and the Caribbean, and morphology (the lower hairiness of its pedipalps, which are more oval in shape, and the presence of only eight rows of denticles in the pedipalp fixed finger) [50].

The difficulties associated with the identification of true populations of C. margaritatus are probably the origin of the conflicting reports of its venom lethality towards vertebrates. Marinkelle and Stahnke [52] reported a median lethal dose (LD50) in mice of 59.9 mg/kg (intraperitoneally) from a C. margaritatus Colombian population, whereas Gómez et al. [53] has reported a lethal titer in mice of 5.19 mg/kg for the same species but from a Costa Rican population. Central American C. margaritatus populations now belong to C. edwardsii [50]. As to the Ecuadorian populations of C. margaritatus, venom from specimens collected in Guayaquil has been shown to decrease significantly the cardiac frequency when injected subcutaneously into rabbits [54]. Campos [14] also reports on severe manifestations on a human adult envenomed by C. margaritatus in Playas, province of Guayas, who experienced vomiting, intense dyspnea, shivering, and numbness of the tongue [14]. Despite these observations, no modern reports have been published on envenoming by C. margaritatus in Ecuador. One recent adult case of C. margaritatus envenoming in Guayaquil presented with paresthesia and erythema at the sting site (Dr. Miguel Delgado, Postgraduate Program in Intensive Care, Universidad Espíritu Santo, Guayaquil, personal communication).

Material collected

In peridomiciliary areas in the cities of Portoviejo (1.316S, 80.2716 W) (n = 7; 3♀♀, 4♂♂) and Chone (0.4153S, 80.537 W) (n = 10; 6♀♀, 4♂♂), both in the lowland area of the province of Manabí (14.XII.2014, A. Borges coll). These findings extend C. margaritatus distribution range to this province; mild envenomings by this species are common in both cities. Specimens of C. margaritatus have also been collected in the metropolitan areas of Quevedo (1.02863S, 79.46352 W) (n = 10, 2♀♀, 8♂♂; 5.VIII.2014, T. Escobar coll.), and Babahoyo (1.80217S, 79.53443 W) (n = 10, 3♀, 7♂; 20.VIII.2014, T. Escobar coll.), both in the province of Los Ríos.

Genus Tityus

Tityus is unquestionably the most complex genus of scorpions from a taxonomical standpoint (over 200 described species), accountable for the majority of severe and lethal scorpionism cases in Central and South America and the Caribbean, including Ecuador, due to the high lethality of their venoms towards vertebrates (intraperitoneal LD50 for mice ranging from 0.7 to 12 mg/kg) [22, 47, 5557]. The genus has been divided into the subgenera Archaeotityus Lourenço, Atreus Gervais, Brazilotityus Lourenço, and Tityus Koch to accommodate taxa previously assigned to the morphological groups “androcottoides,” “asthenes,” “bahiensis,” “bolivianus,” “clathratus,” “crassimanus,” “forcipula,” “melanostictus” and “quisqueyanus” [58].

In Ecuador, the majority of Tityus species (n = 16) belong to subgenera Atreus (n = 5) and Tityus (n = 7), with four taxa corresponding to the subgenus Archaeotityus. Species within Atreus belong to either the morphological groups “Tityus forcipula” (n = 2), “Tityus asthenes” (n = 2), or “Tityus androcottoides” (n = 1) whereas all species within the subgenus Tityus belong to the “Tityus bolivianus” complex. Described Ecuadorian Tityus spp. are mostly from the “Sierra” (n = 9) and “Oriente” provinces (n = 7), with only one record – Tityus (Atreus) asthenes Pocock – from the coastal province of Esmeraldas (Fig. 1). Some representatives of the Ecuadorian Tityus fauna are depicted in Fig. 4. We have excluded Tityus (Atreus) spinatus Pocock from the list of Ecuadorian species since this was synonymized with Tityus (Atreus) forcipula Pocock by Lourenço [59] and was not included by Fet et al. [41] in their catalog of world scorpions. Lourenço and Ythier [17] indicated, however, that T. (A.) spinatus is a species associated with the “Tityus forcipula” group but provided no details regarding its validity [17].

Fig. 4
figure 4

Tityus and Hadruroides species inhabiting Ecuador. a Tityus (A.) bastosi – subgenus Archaeotityus (male, picture taken by Richard C. West); b Tityus (T.) ecuadorensis - “Tityus bolivianus” group (female, picture taken by Michiel Cozijn); c Tityus (A.) ythieri – “Tityus androcottoides” group (male, picture taken by Eric Ythier); d Tityus (T.) pugilator – “Tityus bolivianus” group (male, picture by Jan Ove Rein); e Tityus (T.) roigi – “Tityus bolivianus” group (male from Baños de Agua Santa, Tungurahua province, picture by Radomir Jirsak), f Tityus (A.) asthenes – “Tityus asthenes” group (male from Shushufindi, province of Sucumbíos, picture by A. Borges; g Tityus (A.) forcipula – “Tityus forcipula” group (female, picture taken by Michiel Cozijn); h Hadruroides (L.) charcasus (Karsch) (from Macará, El Oro province, Ecuador; picture by Radomir Jirsak)

  1. 1.

    Tityus (Atreus) asthenes Pocock, 1893:313.

    This species (Fig. 4 – f) was described from a specimen collected in “Pororu,” Peru, by Pocock [60], but no contemporary locality with this name exists in this country. It has been suggested that the correct locality is Paruro, in the department of Puno, southern Peru [61], although no modern records of T. (A.) asthenes exist for this region, where Tityus (Tityus) soratensis Kraepelin is the only Tityus species reported thus far [62]. More recent Peruvian records for T. (A.) asthenes are supplied by Teruel [63], from Capahuari, province of Loreto, on the border with Ecuador. T. (A.) asthenes presents a disjointed distribution in Ecuador (cis- and trans-Andean), since it inhabits the western and eastern versants of the Andes range, having been reported from the western province of Esmeraldas and the eastern province of Napo [18].

    Considering its abundance in the areas where accidents have taken place, T. (A.) asthenes is probably the species associated with the severe and fatal accidents in children from the provinces of Sucumbíos and Morona Santiago (A.B., unpublished observations). T. (A.) asthenes has been found from Peru to Panama, having produced severe envenoming cases and fatalities in Colombia [64] and Panama [47, 65]. T. (A.) asthenes neurotoxins from the Panamanian populations are only weakly recognized by the anti-Tityus (Tityus) serrulatus (Brazil) and anti-Tityus (Atreus) discrepans (Venezuela) antivenoms [66]. A test of the immunological reactivity of venom from Ecuadorian populations of T. (A.) asthenes towards available antivenoms is pending.

Material collected

Shushufindi, province of Sucumbíos (n = 5, 2♀♀, 3♂♂; 31/VII/2014, inside rural housing, T. Escobar coll.), thereby extending T. asthenes distribution range to this province in Ecuador.

  1. 2.

    Tityus (Archaeotityus) bastosi Lourenço, 1984:358–359.

    This species (Fig. 4 - a) belongs to the subgenus Archaeotityus, which comprises highly pigmented scorpions (formerly in the “Tityus clathratus” morphological group), the smallest (18–40 mm) and most ancient group of species in this genus, in which the subaculear tooth is always rhomboidal. Type material of T. bastosi is from Los Tayos, province of Morona Santiago; also reported from Coca (Puerto Francisco de Orellana, 0.46289S, 76.9868 W), province of Napo, amply distributed in the Amazonian regions of Brazil (São Paulo de Olivença, state of Amazonas) and Peru (Iquitos, department of Loreto) [67].

  1. 3.

    Tityus (Atreus) crassicauda Lourenço & Ythier, 2013:2–9.

    Type material from Tandayapa (0.01667S, 78.76667 W), Pichincha Province [17]. T. crassicauda belongs to the “Tityus forcípula” morphological group (in the subgenus Atreus), which comprises medium- to large-sized (above 50 mm), reddish-brown (in adults) species, characterized by the presence of strong spinoid granules at the end of dorsal metasomal carinae [59]. The group encompasses several Tityus spp. such as Tityus (Atreus) fuhrmanni Kraepelin, Tityus (Atreus) metuendus Pocock, Tityus (Atreus) pachyurus Pocock, Tityus (Atreus) macrochirus Pocock, and Tityus (Atreus) festae Borelli, all [with the exception of T. (A.) macrochirus] known to be responsible for high morbidity and pediatric mortality across their distribution range in Panama, Colombia, and Peru [22, 47, 56]. The epidemiological status of the Ecuadorian species in the “Tityus forcipula” group has not yet been determined.

  1. 4.

    Tityus (Tityus) demangei Lourenço, 1981:640–644.

    Holotype from Cueva de los Tayos, province of Morona Santiago. This species belongs to the “Tityus bolivianus” morphological group (in the subgenus Tityus), which includes medium to large-sized (40–70 mm), yellowish/chestnut brown species, distributed along the foothills of the Andes, from Ecuador to northern Argentina and Uruguay [68].

  1. 5.

    Tityus (Tityus) ecuadorensis Kraepelin, 1896:127–129.

    Fet et al. [41] reported Piscobamba, in the province of Loja, Ecuador, as the type locality for this species. There is no such locality in Ecuador but rather in the Peruvian province of Áncash. Instead, the river Piscobamba (4.1447S, 79.1756 W), may be the site of type collection in Ecuador, located east of Malacatos, southern section of the province of Loja. Also reported from Landangui (4.20521S, 79.22455 W) (Loja province) and Zaruma (El Oro province) (3.69132S, 79.61174 W). This species (Fig. 4 ‐ b) also belongs to the “Tityus bolivianus” complex and is a shared species with Peru, where has been collected in the departments of Cajamarca and Cuzco [68].

  1. 6.

    Tityus (Atreus) forcipula (Gervais, 1844:130)

    Type material from an unknown locality in Colombia [41]. This species (Fig. 4) is distributed from southwestern Colombia (department of Cauca) to northwestern Ecuador (provinces of Pichincha, Santo Domingo de Tsáchilas, and Cotopaxi) [18, 69]. T. (A.) forcipula is the type species of the “Tityus forcipula” morphological group.

  1. 7.

    Tityus (Tityus) gasci Lourenço, 1981:841–845.

    Holotype from southern French Guyana [70]. The species is reported from Cuyabeno, in the province of Napo, a locality that currently lies in the province of Sucumbíos (0.25911S, 75.89398 W). The species is amply distributed in the Amazon Basin, from French Guyana and Brazil to Ecuador and Peru.

  1. 8.

    Tityus (Archaeotityus) intermedius Borelli, 1899:8–10.

    Type material from the city of Ibarra, province of Imbabura, northern Ecuador. This species has been reported from Colombia but it has not been included on recent lists of Colombian Tityus species and is hereby considered endemic in Ecuador [10, 69, 71].

  1. 9.

    Tityus (Archaeotityus) julianae Lourenço, 2005:222–224.

    Holotype from the Valley of river Cayapas, west of San Miguel, province of Esmeraldas (0.7436S, 78.91506 W) [27].

  1. 10.

    Tityus (Tityus) jussarae Lourenço, 1988:686–688.

    Holotype from Cueva del Lagarto, near Mondayacu (0.4936S, 77.4617 W), province of Napo, and also from Cueva San Bernardo, in the same province. The species belongs to the “Tityus bolivianus” group of species.

  1. 11.

    Tityus (Tityus) pugilator Pocock, 1898:413–414.

    Holotype from “Cachavi,” Ecuador. The correct locality is actually San Javier de Cachaví, northwestern section of the Esmeraldas province (1.0358 N, 78.4638 W). Also collected from near the cave of Rumichaca de la Paz (“La Gruta de la Paz,” 0.301797 N, 77.50481 W), 18 km north of San Gabriel, in the province of Carchi, Cumbayá (valley of Tumbaco) (province of Pichincha), river Guayllabamba, near Quito (province of Pichincha), and from Ibarra (province of Imbabura) [18, 19] (Fig. 4). It belongs to the “Tityus bolivianus” species complex.

  1. 12.

    Tityus (Tityus) roigi Maury & Lourenço, 1987:80–84.

    Holotype collected in Baños (currently Baños de Agua Santa, 1.39639S, 78.42472 W), province of Tungurahua [72, 73]. The species belongs to the “Tityus bolivianus” complex.

  1. 13.

    Tityus (Archaeotityus) silvestris Pocock, 1897:363–364.

    The original description of this species was based on a specimen collected in Santarém, state of Pará, Brazil [74]. It is distributed along the Amazon basin from French Guyana, and has been reported in Ecuador although no precise collection localities have been mentioned [17, 75]. In the maps published by Lourenço et al. [17, 27], T. silvestris is roughly assigned to the eastern section of the province of Orellana.

  1. 14.

    Tityus (Tityus) simonsi Pocock, 1900:469–470.

    Type material is from the city of Loja, province of Loja [6]; the species has also been reported in Vilcabamba, province of Loja (4.26233S, 79.22287 W) [76]. This species is shared with northern Peru [68]. It is a very close taxon to T. (T.) ecuadorensis to the point that hybridization experiments have been suggested to determine whether T. simonsi could be a morph of the latter species [68].

  1. 15.

    Tityus (Atreus) timendus Pocock, 1898:414.

    Type material from San Javier de Cachaví, Esmeraldas province. Although restored by Lourenço [77], T. (A.) timendus was not included in a recent revision of the Ecuadorian Tityus fauna [17]. Thus, the species is included on the list of current species from Ecuador (Fig. 2). T. (A.) timendus has been placed in the “Tityus asthenes” species complex in the subgeneus Atreus, but has also been cited as an allied species of T. (A.) pachyurus [77], which is responsible for severe envenomings in Colombia and Panama [47, 78].

  1. 16.

    Tityus (Atreus) ythieri Lourenço, 2007:377–380.

    Holotype from south of Yaupi (2.85444S, 77.936 W), province of Morona Santiago (Fig. 4). It is the only Tityus species thus far described from Ecuador that belongs to the “Tityus androcottoides” morphological group, which comprises scorpions with ventral keels of metasomal segments II to IV partly or largely fused [28]. Species within this group are generally restricted to the east of the Colombian Eastern Cordillera and mainly inhabit the Venezuelan mountainous range [79] and a few have been described from the Brazilian Amazonia [Tityus (Atreus) elizabethae Lourenço & Ramos, Tityus (Atreus) neblina Lourenço] and eastern Colombia [Tityus (Atreus) rebierei Lourenço] [28, 71].

Most species within this group produce highly toxic venoms and are accountable for severe/lethal scorpionism, mainly in Venezuela [22]. Kovařík et al. [76] synonymized T. (A.) ythieri to Tityus (Atreus) magnimanus Pocock, based on a genetic and morphological comparison, but the species was later reinstated by Ythier [80] on the basis of a misidentification of the T. (A.) ythieri specimens studied by Kovařík et al. [76].

Family Caraboctonidae

Genus Hadruroides

Species of Hadruroides (n = 22) are restricted to Ecuador, Peru, northern Chile, and several offshore islands (including the Galápagos), where they inhabit inter-Andean valleys, Pacific deserts, and dry forest habitats [32, 81]. In Ecuador the genus is represented by seven species, recently split into two subgenera by Rossi [32]. The nominal subgenus, Hadruroides, now includes only one species, Hadruroides (Hadruroides) charcasus (Karsch), whereas the subgenus Lourencoides Rossi includes all other known species. The total number of Hadruroides species inhabiting mainland Ecuador is now raised to six [32].

Ecuadorians records of Hadruroides (Lourencoides) lunatus (Koch) [82] are suggested to be probable misidentifications of other Hadruroides species, which is also the case in reports of this species from northern Chile [81]. Records of Hadruroides (Lourencoides) leopardus Pocock from the city of Loja, province of Loja [18], are probably referencing Hadruroides (Lourencoides) udvardyi Lourenço [81].

Species in this genus appear to be weakly toxic to vertebrates upon peripheral venom injection, as shown in the case of H. (L.) lunatus (from Lima, Peru) based on the low lethality (LD50 = 22 mg/kg) of its venom when injected intraperitoneally in mice. H. (L.) lunatus venom is, however, highly toxic upon central injection (LD50 = 0.1 mg/kg) [83]. Although Hadruroides venoms are not lethal to mammals, at least peripherally, they probably contain components able to elicit heart muscle disruption in vertebrates.

Serum levels of total creatine kinase (CK) and its isoenzyme MB (CK–MB), two widely accepted markers for heart injury or myocardial infarction, have been found significantly elevated in rats envenomed intraperitoneally with a sublethal dose of H. (L.) lunatus venom (5.8 mg/kg) [83]. Venom from another species, H. (H.) charcasus (Karsch) (from northern Peru), produces in the heart of Bufo spinulosus (Amphibia, Bufonidae) cellular necrosis, leukocyte infiltration, and endothelial lesions without significantly altering the cardiac force or frequency [84]. The actual clinical implications of these results are not yet clear, but these activities are probably due to the presence in venoms from Hadruroides spp. of low-molecular-weight neurotoxins and/or phospholipase components [83].

  1. 1.

    Hadruroides (Hadruorides) charcasus (Karsch, 1879:135)

    Holotype from Bolivia, from an unknown locality [41]. The species was redescribed by Maury [82] using material collected in the province of Cajamarca, northern Peru [82]. Rossi [32] reports this species from Macará, province of Loja (4.38181S, 79.9437 W) (Fig. 4).

  1. 2.

    Hadruroides (Lourencoides) doriai Rossi, 2014:206–207.

    Type material from San Pedro, county of Arenillas, El Oro province, in the border with Peru (3.66671S, 80.10142 W).

  1. 3.

    Hadruroides (Lourencoides) elenae Rossi, 2014:198–202.

    Holotype from La Puntilla, near Salinas (2.18973S, 81.01074 W), province of Santa Elena.

  1. 4.

    Hadruroides (Lourencoides) galapagoensis Maury, 1974:19.

    Endemic to the Galápagos islands [81]. Reported from the islands of Española, Fernandina, Floreana, Isabela, Pinzón, Santa Cruz, Santa Fé, Santiago, and San Salvador [85, 86]. H. (L.) galapagoensis is found from the coastal arid zone up to the arid top zone of the Isabela volcanoes [49].

  1. 5.

    Hadruroides (Lourencoides) maculatus (Thorell, 1876:186).

    Distributed in Ecuador on its central coastline, provinces of Manabí and Guayas, and shared with Peru (holotype from El Callao), H. (L.) maculatus seems to be the most common species of the genus in Ecuador [32, 81, 87]. It has been reported from Manta, and “Machalillo” [correct location is Machalilla (1.2824S, 80.4551 W)], both in the province of Manabí; La Puntilla, province of Santa Elena, and also from the city of Guayaquil, in the Estero del Salado (2.2533S, 80.210 W) [82]. Playas del Morro was mentioned by Campos [14] as a locality where he collected this species in the province of Guayas.

  1. 6.

    Hadruroides (Lourencoides) moreti Rossi, 2014:202–205.

    Type material from San Vicente, province of Bolìvar (1.90818S, 79.24859 W).

  1. 7.

    Hadruroides (Lourencoides) udvardyi Lourenço, 1995:76–78.

    Holotype from the province of Azuay, 90 km in the road from Cuenca to Loja. Endemic to inter-Andean valleys at altitudes above 2,000 m in southern Ecuador, in the provinces of Azuay and Loja [32, 81].

Family Chactidae

Genus Chactas

This exclusively Neotropical genus is distributed from Costa Rica to northern Peru, with Colombia as a possible center of dispersion since most known Chactas species are from this country. A number of species have been described in Venezuela and isolated taxa are reported in Brazil and Peru. Species are also known from Costa Rica, Panama and the Island of Trinidad [29]. There are no species within this genus analyzed from either toxinological or clinical standpoints. The venom from the Neotropical chactid Brotheas amazonicus Lourenço possesses an LD50 in mice (intraperitoneally) of 90 mg/kg, two orders of magnitude above the lethality of venoms from Tityus spp. and twice the lethality of venoms from species in genera Brachistosternus and Hadruroides [57].

  1. 1.

    Chactas mahnerti Lourenço, 1995:70–71.

    Known from La Florida (0.220S, 78.300 W) and San Antonio (0.023S, 78.2648 W), province of Pichincha, and also from Coca, province of Napo [18].

  1. 2.

    Chactas moreti Lourenço, 2014:19–23.

    Type material collected at San Pablo de Kantesiya (0.1515S, 76.2535 W), near the Aguarico River, province of “Sucumbíus” [sic] (Sucumbíos, northern Ecuador) [29].

  1. 3.

    Chactas yaupi Lourenço, 2014:173–177.

    Collected north of the town of Yaupi (2.5116S, 77.569 W), between Yaupi and Morona, province of Morona Santiago [31].

Genus Teuthraustes

All the species of Teuthraustes so far described (n = 24) have been collected in the Andean mountains of Ecuador, Peru and Colombia, and in the Amazonian highlands of Venezuela and Brazil, with the highest species diversity corresponding to Ecuador. Even though the taxonomic validity of some of these taxa will probably be the subject of further scrutiny, the outstanding concentration of species in Ecuador is realistic [20]. In their transferring of Chactas camposi Mello-Leitão to the genus Teuthraustes, Ochoa and Pinto da Rocha [30] presented a list of the 11 Ecuadorian species thus far reported, together with their provinces of origin. The following account clarifies the origin of some of these species and their geographical distribution.

  1. 1.

    Teuthraustes atramentarius Simon, 1878:400.

    This species is widespread in the provinces of Cotopaxi, Ibarra, and Pichincha (Fig. 3), and is certainly the most abundant scorpion in the metropolitan area of Quito [88]. Together with C. margaritatus from the coastal region, the abundance of these two species in the most industrialized and populated areas of Ecuador (i.e. Pichincha and Guayas provinces) suggests their responsibility for most scorpion envenomings in these regions. The fact that their venoms are not significantly toxic to vertebrates [52, 89] has been taken to indicate that scorpions are not of medical significance in the country, a situation reminiscent of the weakly toxic, widespread Venezuelan species, Rhopalurus laticauda (Thorell) [79]. In fact, T. atramentarius envenoming in humans only produces local symptomatology, resembling a bee sting [90].

  1. 2.

    Teuthraustes camposi (Mello-Leitão, 1939:147–148).

    The type locality for this species has been assigned by Ochoa and Pinto da Rocha [30] to the province of Cañar, northern Ecuador, but the precise location is not known. The type material of T. camposi was donated by the Ecuadorian entomologist Francisco Campos to C. de Mello-Leitão, at the Rio de Janeiro National Museum (MNRJ), who identified it as belonging to the genus Chactas [10]. Ochoa and Pinto da Rocha [30] later assigned the specimen to the genus Teuthraustes and stated that the type material at the MNRJ was originally labeled “Chactas rosenbergi Pocock.” In his 1931 account of Ecuadorian scorpions, Campos reports that the material classified as Chactas rosenbergi Pocock was collected in Bucay and Chimbo, in the provinces of Guayas and Bolívar, respectively, and that samples of “Chactas sp.” were obtained at Gualea (0.11677 N, 78.7476 W), in the province of Pichincha. There is no mention in his review of collection sites in the province of Cañar [14]. A further search for this species in the provinces of Cañar, Bolívar, Guayas, and Pichincha is pending to determine its true distribution range.

  1. 3.

    Teuthraustes dubius (Borelli, 1899:14).

    The type locality (“Valle de Santiago”) for this species was placed by Borelli [7] in “eastern Ecuador” without further details on its location. Borelli´s locality most probably refers to the channel of river Santiago, which originates in Ecuador from the union of two rivers, the Namangoza and the Upano, in the province of Morona Santiago, Ecuadorian Amazonia, where it flows 55 km before reaching the current border with Peru. The collector, Italian zoologist Enrico Festa, commented that the places where he collected in the Valle del Santiago were not far from the Marañón River, now belonging to Peru [90]. Back in the 1890s the area between the two rivers was under the jurisdiction of Ecuador. The species range of distribution includes the Cueva de los Tayos, also in Morona Santiago [44].

  1. 4.

    Teuthraustes festae (Borelli, 1899:11).

    This species was also collected by Enrico Festa in Valle del Santiago, province of Morona Santiago.

  1. 5.

    Teuthraustes gervaisii (Pocock, 1893:82).

    Type material from the city of Cuenca, the capital of the Azuay province [41, 60]. Also collected in the ruins of Ingapirca (2.54435S, 78.87741 W), between Cañar and El Tambo, province of Cañar, at 2,800 m altitude [91].

  1. 6.

    Teuthraustes lojanus (Pocock, 1900:472–473).

    Holotype collected from Loja, capital city of the province of Loja.

  1. 7.

    Teuthraustes oculatus Pocock, 1900:473.

    Type material collected from Sinche and Riobamba [6, 41]. Several towns named “Insinche” in Ecuador from the province of Cotopaxi, north of the province of Chimborazo (where the second locality, Riobamba, is placed), are candidates for the first locality. To the best of our knowledge, no records of this species exist from the Tungurahua province, as reported by Ochoa and Pinto da Rocha [30].

  1. 8.

    Teuthraustes ohausi Kraepelin, 1912:73,77-78.

    In his description of the species, Kraepelin [8], and also Fet et al. [41], refer to “Calamayo,” as its type locality, but the correct location is Catamayo (3.5911S, 79.2132 W), 36 km west of Loja, province of Loja.

  1. 9.

    Teuthraustes rosenbergi (Pocock, 1898:419–420).

    Holotype from Chimbo, near Guayaquil. Pocock [5] refers “Chimbo” as the type locality for this species, which actually corresponds to San José de Chimbo (1.410S, 79.133 W), province of Bolívar, 16 km south of Guaranda, the provincial capital. Campos [14] also reports this species from Bucay (2.100S, 79.600 W), province of Guayas, 100 km west of Guayaquil. He reports that T. rosenbergi is very abundant under the bark of fallen logs, together with insects from the order Dermaptera.

  1. 10.

    Teuthraustes simonsi (Pocock, 1900:471–472).

    Holotype from “Río Amboque,” Ecuador. This locality, given by Pocock [6] without further details, has no contemporary counterpart in Ecuadorian geography. Ochoa and Pinto da Rocha [30] assigned this species to the province of Carchi but an exhaustive search of current towns and rivers in this province has not rendered any similarities to this name.

  1. 11.

    Teuthraustes whymperi (Pocock, 1893:90).

    The type locality, “Millegalli,” is in fact the town of Nanegalito (0.356 N, 78.4048 W), in the northwestern section of the province of Pichincha. According to Lourenço [18], T. whymperi is a highly abundant scorpion in Las Pampas, northern section of the province of Cotopaxi. Also reported from the province of Pichincha [18, 30] and from Santo Domingo de los Tsáchilas and Tungurahua provinces [18].

  1. 12.

    Teuthraustes wittii (Kraepelin, 1896:141–144).

    As in the case of Tityus (T.) ecuadorensis, “Piscobamba” is referenced as the type locality for this species, but instead the river Piscobamba is the probable site of collection in the province of Loja. This species has also been reported from the cities of Loja and Vilcabamba, also in the Loja province, and from Zaruma (3.4128S, 79.3642 W), province of El Oro [18].

Family Troglotayosicidae

Genus Troglotayosicus

The genus includes two troglomorphic species (i.e., with morphological adaptations to life in cavernicolous habitats, e.g., the absence of median eyes), one described from Ecuador and a second from the neighboring Colombian department of Nariño, Troglotayosicus humiculum Botero-Trujillo & Francke, 2009 [92]. Medical significance of species in this genus is probably poor given their restricted cavernicolous distribution.

  1. 1.

    Troglotayosicus vachoni Lourenço, 1981:651–656.

    Holotype found in Cueva de los Tayos, province of Morona Santiago [44].

Concluding remarks

Surrounded by areas where scorpion stings are frequent and usually inflicted by noxious species, such as southern Colombia and the Brazilian Amazonia, there was a need to update the list of the scorpion fauna from Ecuador, and establish their geographic distribution and potential medical significance in light of recent accidents in children, some of them fatal [93, 56]. As noted before, insufficient efforts have been made, particularly in the case of the genus Tityus, to correlate human incidents and the precise geographical distribution of the species involved [94]. Preparation of a risk map for scorpionism in Ecuador and the possible manufacturing of a scorpion antivenom effective in the country would be facilitated by establishing such a correlation.

This work updates the number of Ecuadorian scorpion species to 47 and clarifies their distribution by biogeographic area and political provinces upon a thorough revision of individual collection localities based on contemporary records, summarized in Fig. 1. Such clarification should be helpful in future re-collections of specimens. This work also raises the number of endemic taxa to 35 (74.5 % of endemism), a rate comparable to that of Colombia (75.6 %) and only surpassed in northern South America by Venezuela (91.3 %) [79, 95]. For instance, Ecuador has been recognized as the probable center of dispersion for the scorpion genus Teuthraustes, in the family Chactidae, with half of the described species (n = 12) being endemic to the country [20]. Such dynamic speciation of Ecuadorian scorpions has been attributed to an evolutionary mode involving genetic drift in small founder populations, as the plant genera Gasteranthus (Gesneriaceae) and Anthurium (Araceae), with 25 and 50 %, respectively, of their world total species endemic to the environs of Ecuador [17, 9698].

The incidence of scorpion stings in endemic areas is the result, among other factors, of the distribution areas of noxious species, their local abundance and ecology. The most speciose scorpion genera in Ecuador are Tityus (16 spp.), Teuthraustes (12 spp.), and Hadruroides (7 spp.), followed by Ananteris (3 spp.), Brachistosternus (2 spp.) and Centruroides (2 spp.), notwithstanding differences in their relative abundance among the biogeographical areas of “Costa,” “Sierra” and “Oriente” (Fig. 2). Scorpions in the genus Hadruroides are very abundant along the hyperxerophitic coastal areas (in provinces of El Oro, Guayas, and Santa Elena) and can be found under stones and dry manure [14]. There are no reports on the abundance of Ecuadorian Brachistosternus spp. but they are common in dunes of the Peruvian central and northern coast and should present a similar ecology in Ecuador, at least in the case of B. (B.) ehrenbergii [34]. Species in the genus Teuthraustes in Ecuador are mostly forest-dwelling taxa, native to the inter-Andean valleys, and are not hazardous to humans as shown in the case of T. atramentarius, a synanthropic, abundant species in the area of Quito, province of Pichincha [88, 89]. As stated above, C. margaritatus is the most common species found in domiciliary environments along the Ecuadorian coast and in populated areas such as Guayaquil and Milagro (province of Guayas), Babahoyo and Quevedo (province of Los Ríos), Portoviejo, Manta, and Chone (province of Manabí). Ananteris spp. are mostly sylvatic species. Specimens of Tityus spp. are abundant in domiciliary and peridomiciliary habitats of rural communities located in tropical and subtropical rain forest areas of Sucumbíos and Morona Santiago (“Oriente” area) and also in the province of Esmeraldas (“Costa” area), where they have been responsible for severe and lethal cases of scorpionism.

Traditionally, scorpions were not considered dangerous in Ecuador and their sting was supposedly fiercer if specimens from the coastal areas were involved, based on the notion that species from drier places produce venoms with higher toxicity [99]. Regardless of the species, envenoming manifestations in humans, which were claimed to be predominantly local, were reported to resemble those derived from wasp or bee stings [99]. Such an assumption, which has prevailed in modern times, is a consequence of the low toxicity towards vertebrates of the venoms produced by C. margaritatus and T. atramentarius, which are the most common urban species in the country. It is clear from the above account that noxious scorpion species inhabit Ecuador and are capable of producing significant morbidity and pediatric mortality.

According to the species involved, their areas of distribution and the available knowledge of the venom action and composition of allied taxa, as presented in this annotated checklist, we propose a classification of the Ecuadorian scorpion fauna as follows:

  1. 1.

    Species in genera Hadruroides, which are mainly coastal (Fig. 4), would produce severe accidents only if envenoming occurs by a central pathway. Local manifestations such as intense pain, edema and ulceration are expected [100]. Venoms of Hadruroides spp. contain cytotoxic components that may produce heart muscle disruption. Sting by Brachistosternus spp., also a coastal species in Ecuador [with the exception of B. (B.) pegnai, restricted to Carchi], and recognized by their generally clear and yellowish coloration, produces intense pain in humans without further complications, although some venoms contain neurotoxins that can produce autonomic effects [35].

  2. 2.

    Species in genera Centruroides and Teuthraustes inhabiting Ecuador, particularly C. margaritatus and T. atramentarius (Fig. 3) appear not to produce venoms significantly toxic to humans. For instance, envenoming by the C. margaritatus population inhabiting the surroundings of Cali, Colombia – morphologically related to the populations prevalent in the coastal regions of Ecuador [101] – produce intense pain, some discoloration at the sting site, and fever (average 39 °C) 3 to 4 h after the accident, without further complications [52]. T. atramentarius appears to be weakly ly toxic to humans [89].

  3. 3.

    Species in the genus Tityus differ in their venom toxicity towards humans depending on the morphological group to which they pertain:

  4. (a)

    Species belonging to the subgenus Archaeotityus (encompassing the “Tityus clathratus” group) comprise small (18–40 mm), highly pigmented scorpions capable of producing toxins with a fingerprint structurally similar to noxious Tityus spp. [e.g. Tityus (Archaeotityus) clathratus Koch] but they are not considered medically significant due to the low amount of venom injected [102]. In Ecuador these species are T. (A.) julianae, T. (A.) intermedius, T. (A.) bastosi, T. (A.) pugilator, and T. (A.) silvestris.

  5. (b)

    Species in the subgenus Atreus in Ecuador belong either to the morphological groups “Tityus forcípula” [T. (A.) forcipula, T. (A.) crassicauda, and T. (A.) timendus], “Tityus androcottoides” [T. (A.) ythieri], or “Tityus asthenes” [T. (A.) asthenes]. These species seem to be restricted to lowland rain forests of the piedmont east and west of the Andes. Most severe/lethal envenoming cases in northern South America, the Amazonian region, and Central America are due to species in this subgenus [47, 55, 56]. The medically significant Ecuadorian species are most probably all contained within this subgenus.

  6. (c)

    Species in the subgenus Tityus in Ecuador mainly belong to the “Tityus bolivianus” complex [T. (T.) demangei, T. (T.) ecuadorensis, T. (T.) roigi, T. (T.) simonsi, and T. (T.) jussarae], with the exception of T. (T.) gasci. This complex contains species mostly inhabiting the inter-Andean valleys in the “Sierra” region [18]. In contrast to the “Tityus asthenes” and “Tityus forcipula” complexes, no species within the “Tityus bolivianus” group have yet been reported to present medical significance in Ecuador or the countries where this complex is also prevalent (Peru, Bolivia, Argentina).

  7. 4.

    Species of the genera Centruroides (C. exsul) and Hadruroides [H. (L.) galapagoensis] inhabiting the Galápagos archipelago are not considered dangerous to humans although their sting is painful [103].

As severe envenoming cases have been recorded from east of the Ecuadorian Andes, a study of the immunological reactivity of venoms from medically significant species towards available scorpion antivenoms is required to establish their neutralization capacity or whether new antibodies are needed [24]. In this sense, only three anti-Tityus antivenoms are available: anti-Tityus (Atreus) discrepans (Venezuela), anti-Tityus (Tityus) serrulatus (Brazil), and anti-Tityus (Tityus) trivitattus (Argentina) [21, 55]. More collection work is necessary in regions still poorly sampled, such as the provinces of Pastaza and Zamora Chinchipe where no species have been reported thus far (Fig. 1). In this context, it seems reasonable to assume that a significant part of the Ecuadorian scorpion fauna (and their molecules) is still undiscovered, as pointed out recently in relation to other arachnid groups [104].


  1. Mittermeier RA, Mittermeier CG, Gil PR, García-Urtiaga MJ, Flores De Clavé L, Bolívar A. Megadiversidad: los países biológicamente más ricos del mundo. México: Cemex, Conservation International and Agrupacion Sierra Madre; 2009.

    Google Scholar 

  2. Sierra R, Campos F, Chamberlin J. Assessing biodiversity conservation priorities: ecosystem risk and representativeness in continental Ecuador. Landscape Urban Plan. 2002;59(2):95–110.

    Article  Google Scholar 

  3. Dupérré N. Arachnids of Ecuador. 2014.

    Google Scholar 

  4. Sissom WD, Hendrixson BE. Scorpion biodiversity and patterns of endemism in northern Mexico. In: Cartron J-LE, Ceballos G, Felger RS, editors. Biodiversity, ecosystems, and conservation in northern Mexico. Oxford: Oxford University Press; 2005. p. 122–37.

    Google Scholar 

  5. Pocock RI. Descriptions of some new scorpions from Ecuador. Ann Mag Nat Hist, Sér 7. 1898;6(1):413–22.

    Google Scholar 

  6. Pocock RI. Some new or little-known Neotropical scorpions in the British Museum. Ann Mag Nat Hist, Sér 7. 1900;5:469–78.

    Google Scholar 

  7. Borelli A. Viaggio del Dr. Enrico Festa nell'Ecuador e regioni vicine. XVIII: Scorpioni. Boll Mus Zool Anat comp R Univ Torino. 1899;14(345):1–18.

    Google Scholar 

  8. Kraepelin K. Neue Beiträge zur systematik der gliederspinnen. II. Chactinae (Scorpiones). Mitt Naturhist Mus, Beiheft zum Jahrb Hamb Wiss Anst 1911. 1912;29(2):45–88.

    Google Scholar 

  9. Kraepelin K. Beitrag zur kenntnis der skorpione und pedipalpen columbiens. Mém Soc Sci Nat Neuchâtel. 1912;5:15–28.

    Google Scholar 

  10. Mello-Leitão C. Escorpiões Sul-americanos. Arq Mus Nac, Rio de Janeiro. 1945;XL:1–453.

    Google Scholar 

  11. Kraepelin K. Neue und weniger bekannte skorpione. Mitt Naturhist Mus, Beiheft zum Jahrb Hamb Wiss Anst. 1896;13:119–46.

    Google Scholar 

  12. Simon E. Études arachnologiques. 9e Mémoire. XV. Descriptions de deux noveaux genres de l´ordre des Scorpiones. Ann Soc Entomol Fr. 1878;5(8):399–400.

    Google Scholar 

  13. Mello-Leitão C. Una nueva especie de alacrán del género Chactas. Physis. 1939;17:147–8.

    Google Scholar 

  14. Campos RF. Breve contribucion al conocimiento de los Escorpionidos (Alacranes) del Ecuador. Rev Colegio Nac Vicente Rocafuerte. 1931;13(44):117–25.

    Google Scholar 

  15. Campos RF. Notas teratoartropológicas. Caso de un alacrán (Centrurus margaritatus, Gerv.), con diartrosis femoro-tibial en un palpo maxilar. Rev Chil. Hist Nat. 1930;280–281.

  16. Behr-Castillo H, Correa O. Identificacion de los alacranes de la familia Buthidae en la Urbanización Puerto Azul. Guayaquil Rev Ecuat Hig Med Trop. 1987;37:71–6.

    Google Scholar 

  17. Lourenço WR, Ythier E. The remarkable scorpion diversity in the Ecuadorian Andes and description of a new species of Tityus C. L. Koch, 1836 (Scorpiones, Buthidae). ZooKeys. 2013;307:1–13.

    Article  PubMed  Google Scholar 

  18. Lourenço WR. Les scorpions (Chelicerata, Scorpiones) de l´Equateur avec quelques considerations sur la biogeographie et la diversite des especes. Rev Suisse Zool. 1995;102(1):61–88.

    Google Scholar 

  19. Lourenço WR. La faune des scorpions de l´Equateur. I. Les Buthidae. Systématique et biogéographie. Rev Suisse de Zool. 1988;95(3):681–97.

    Google Scholar 

  20. Lourenço WR, Duhem B. The geographical pattern of distribution of the genus Teuthraustes Simon (Scorpiones, Chactidae) in South America and description of a new species. C R Biol. 2010;333(11–12):858–63.

    Article  PubMed  Google Scholar 

  21. Borges A, Bermingham E, Herrera N, Alfonzo MJ, Sanjur OI. Molecular systematics of the neotropical scorpion genus Tityus (Buthidae): the historical biogeography and venom antigenic diversity of toxic Venezuelan species. Toxicon. 2010;55(2–3):436–54.

  22. Borges A, Graham MJ. Phylogenetics of scorpions of medical importance. In: Gopalakrishnakone P, Calvete JJ, editors. Venom genomics and proteomics. Dordrecht: Springer Netherlands; 2015.

    Google Scholar 

  23. Lourenço WR, Leguin E-A. Le véritable statut de l’espèce Chactas rubrolineatus Simon, 1880 (Scorpiones: Chactidae). Rev Iber Arachnol. 2014;24:87–9.

    Google Scholar 

  24. Hospital General de Macas. Province of Morona Santiago: Ministerio de Salud Publica. Accessed 20 Feb 2015.

  25. Cekalovic KT. Brachistosternus pegnai n. sp. de escorpión para el Ecuador (Scorpionida-Bothriuridae). Bol Soc Biol Concepción. 1969;41:163–71.

    Google Scholar 

  26. Lourenço WR. Some remarks about Ananteris festae Borelli, 1899 and description of a new species of Ananteris Thorell from Ecuador (Scorpiones, Buthidae). Ent Mitt Zool Mus Hamburg. 1999;13(160):95–100.

    Google Scholar 

  27. Lourenço WR. A new species of Tityus Koch, 1836 (Scorpiones, Buthidae) from Ecuador. Ent Mitt Zool Mus Hamburg. 2005;14(171):221–7.

    Google Scholar 

  28. Lourenço WR. A new species of Tityus C.L. Koch, 1836 from Ecuador: the first element of the ´Tityus androcottoides´ subgroup for this country. Ent Mitt Zool Mus Hamburg. 2007;14(176):375–85.

    Google Scholar 

  29. Lourenço WR. The second confirmed record of the scorpion genus Chactas Gervais, 1844 (Scorpiones, Chactidae) from Ecuador with description of a new species from the Amazonian Province of Sucumbíos. Zookeys. 2014;372:17–26.

    Article  PubMed  Google Scholar 

  30. Ochoa JA, Pinto da Rocha R. On the taxonomic status of Chactas camposi Mello-Leitão, 1939 (Scorpiones, Chactidae). Zootaxa. 2012;3210:61–8.

    Google Scholar 

  31. Lourenço WR. The third confirmed record of the scorpion genus Chactas Gervais, 1844 (Scorpiones, Chactidae) from Ecuador, with description of a new species from the Amazonian Province of Morona Santiago. Ent Mitt Zool MusHamburg. 2014;17(193):171–8.

    Google Scholar 

  32. Rossi A. A revision of the genus Hadruroides Pocock, 1893 in Ecuador mainland with the description of three new species, the definition of a new subgenus and a new record. Ann Mus Civ Stor Nat "G Doria". 2014;106:193–210.

    Google Scholar 

  33. Ojanguren Affilastro A, Ramírez MJ. Phylogenetic analysis of the scorpion genus Brachistosternus (Arachnida, Scorpiones, Bothriuridae). Zool Scr. 2009;38(2):183–98.

    Article  Google Scholar 

  34. Calderón ST, Aguilar PG. Escorpiones y escorpionismo en el Peru. X: Efecto del veneno de Brachistosternus ehrenbergi sobre ratones albinos. Rev Peru Ent. 1988;30:91–3.

    Google Scholar 

  35. Ramos C, Escobar E. Aislamiento y algunas propiedades de la toxina Be1 del veneno de Brachistosternus ehrenbergii (Gervais, 1841) (Scorpiones: Bothriuridae). Rev Peru Biol. 2007;13(3):243–7.

    Google Scholar 

  36. de Lima ME, Martin-Eauclaire MF. The toxins purified from Tityus serrulatus (Lutz & Mello) venom. J Toxicol - Toxin Rev. 1995;14(3):457–81.

    Article  Google Scholar 

  37. Schöttler WHA. On the toxicity of scorpion venom. Am J Trop Med Hyg. 1954;3(1):172–8.

    PubMed  Google Scholar 

  38. Sunagar K, Undheim EAB, Chan AHC, Koludarov I, Muñoz-Gómez SA, Antunes A, et al. Evolution stings: the origin and diversification of scorpion toxin peptide scaffolds. Toxins (Basel). 2013;5(12):2456–87.

    Article  CAS  Google Scholar 

  39. Cekalovic T, Artigas J. Catalogo de los tipos depositados en la coleccion del departamento de zoología de la Universidad de Concepción. Chile Bol Soc Biol Concepción. 1981;51:75–107.

    Google Scholar 

  40. Ochoa JA, Ojanguren Affilastro AA, Mattoni CI, Prendini L. Systematic revision of the Andean scorpion genus Orobothriurus Maury, 1976 (Bothriuridae), with discussion of the altitude record for scorpions. Bull Am Mus Nat Hist. 2011;359:3–90.

    Article  Google Scholar 

  41. Fet V, Sissom WD, Lowe GJ, Braunwalder ME. Catalog of the scorpions of the world (1758–1998). New York: New York Entomological Society; 2000.

    Google Scholar 

  42. Ochoa JA, Ojanguren AA. Systematics and distribution of Brachistosternus (Brachistosternus) ehrenbergii (Gervais, 1841), with the first record of stridulation in the genus Brachistosternus. Stud Neotrop Fauna E. 2007;42(1):61–9.

    Article  Google Scholar 

  43. Froy O, Gurevitz M. New insight on scorpion divergence inferred from comparative analysis of toxin structure, pharmacology and distribution. Toxicon. 2003;42(5):549–55.

    Article  CAS  PubMed  Google Scholar 

  44. Lourenço WR. Scorpions cavernicoles de l´Equateur: Tityus demangei n. sp. et Ananteris ashmolei n. sp. (Buthidae); Troglotayosicus vachoni n. gen., n. sp. (Chactidae), scorpion troglobie. Bull Mus Natl Hist Nat (Paris), sér 4. 1981;3:635–62.

    Google Scholar 

  45. Lourenço WR. Révision du genre Ananteris Thorell, 1891 (Scorpiones, Buthidae) et description de six espèces nouvelles. Bull Mus Natl Hist Nat (Paris). 1982;4(1–2):119–51.

    Google Scholar 

  46. Guerrero-Vargas JA, Ayerbe S, Rada-Mendoza M, Vélez P, Beltran J, D’Suze G, et al. Preliminary toxinological characterization of the venom of the scorpion Centruroides margaritatus (Buthidae, Gervais, 1841) of the valle of the Patía, Colombia. J Venom Anim Toxins incl Trop Dis. 2007;13(1):228.

    Google Scholar 

  47. Borges A. Scorpionism and dangerous scorpions in Central America and the Caribbean region. In: Gopalakrishnakone P, Possani LD, Schwartz EF, Rodriguez De La Vega R, editors. Scorpion venoms. Dordrecht: Springer Netherlands; 2015. p. 215–44.

    Google Scholar 

  48. Lambertz M. On the date and organ of publication for the endemic Galápagos scorpion Centruroides exsul (Scorpiones: Buthidae) by Wilhelm Meise, with a revision of its distribution and type material. J Arachnol. 2013;41(3):412–4.

    Article  Google Scholar 

  49. Baert L, Maelfait J-P, Desender K. Distribution of the arachnid species of the orders Scorpiones, Solifugae, Amblypigi, Schizomida, Opiliones and Pseudoscorpiones in Galápagos. Bull Inst R Sci Nat Belg. 1996;65:5–19.

    Google Scholar 

  50. de Armas LF, Teruel R, Kovařík F. On Centruroides margaritatus (Gervais, 1841) and closely related species (Scorpiones: Buthidae). Euscorpius. 2011;132:1–16.

    Google Scholar 

  51. Sissom WD, Lourenço WR. The genus Centruroides in south America (Scorpiones, Buthidae). J Arachnol. 1987;15:11–28.

    Google Scholar 

  52. Marinkelle CJ, Stahnke HL. Toxicological and clinical studies on Centruroides margaritatus (Gervais), a common scorpion in western Colombia. J Med Entomol. 1965;2(2):197–9.

    Article  CAS  PubMed  Google Scholar 

  53. Gómez A, Bonilla F, Sasa M. Preliminary characterization of venoms from scorpion genera Centruroides and Tityus (Buthidae) from Costa Rica. In: Proceedings of the tenth meeting of the PanAmerican section of the International Society on Toxinology; 2010 Apr 18–22; San José, Costa Rica. San José: International Society on Toxinology. 2010. p. 132.

    Google Scholar 

  54. Alvarez LE, Cevallos E. Efectos del veneno de alacrán sobre el corazón de conejos. Rev Univ Guayaquil. 1986;2(64):60–4.

    Google Scholar 

  55. Pucca MB, Neves Oliveira F, Schwartz EF, Arantes EC, Lira-da-Silva RM. Scorpionism and dangerous species of Brazil. In: Gopalakrishnakone P, Possani LD, Schwartz EF, Rodriguez De La Vega R, editors. Scorpion Venoms. Dordrecht: Springer Netherlands; 2014.

    Google Scholar 

  56. Guerrero-Vargas JA, Buitrago JR, Ayerbe S, Daza Flórez E, Beltrán JTB. Scorpionism and dangerous species of Colombia. In: Gopalakrishnakone P, Possani LD, Schwartz EF, Rodriguez De La Vega R, editors. Scorpion venoms. Dordrecht: Springer Netherlands; 2014.

    Google Scholar 

  57. Nishikawa AK, Caricati CP, Lima ML, dos Santos MC, Kipnis TL, Eickstedt VRD, et al. Antigenic cross-reactivity among the venoms from several species of Brazilian scorpions. Toxicon. 1994;32(8):989–98.

    Article  CAS  PubMed  Google Scholar 

  58. Lourenço WR. Nouvelle proposition de découpage sous-générique du genre Tityus C.L. Koch, 1836 (Scorpiones, Buthidae). Bol Soc Entomol Aragonesa. 2006;39:55–67.

    Google Scholar 

  59. Lourenço WR. Etude systématique de quelques espèces appartenant au complexe Tityus forcipula (Gervais, 1844) (Scorpiones, Buthidae). Bull Mus Natl Hist Nat (Paris). 1984;6(A3):729–39.

    Google Scholar 

  60. Pocock RI. A contribution to the study of neotropical scorpions. Ann Mag Nat Hist. 1893;6(68):77–103.

    Article  Google Scholar 

  61. Francke O. Escorpiones y escorpionismo en el Peru VI: Lista de especies y claves para identificar las familias y los géneros. Rev Peru Entomol. 1977;20:73–6.

    Google Scholar 

  62. Ochoa JA. Patrones de distribución de escorpiones de la región andina en el sur peruano. Rev Peru Biol. 2005;12(1):49–68.

    Google Scholar 

  63. Teruel R. La verdadera identidad de Tityus championi Pocock, 1898 (Scorpiones: Buthidae). Bol Soc Entomol Aragonesa. 2011;48:367–73.

    Google Scholar 

  64. Gómez JP, Quintana JC, Arbeláez P, Fernández J, Silva JF, Barona J, et al. Picaduras por escorpión Tityus asthenes en Mutatá, Colombia: aspectos epidemiológicos, clínicos y toxinológicos. Biomedica. 2010;30(1):126–39.

    Article  PubMed  Google Scholar 

  65. Borges A, Miranda RJ, Pascale JM. Scorpionism in Central America, with special reference to the case of Panama. J Venom Anim Toxins incl Trop Dis. 2012;18(2):130–43.

    Article  Google Scholar 

  66. Borges A, de Sousa L, Acosta De Patiño H, Pascale JM, Miranda R, Castillo C, et al. Proposal for a toxinological partitioning of south and central American species in the genus Tityus (Scorpiones, Buthidae). In: First International meeting Vital para o Brasil, 3–6 sept 2013, Niterói – RJ. 1st International meeting Vital para o Brasil about venomous animals. 2013.

    Google Scholar 

  67. Lourenço WR. Analyse taxonomique des scorpions du groupe Tityus clathratus Koch, 1845 (Scorpiones, Buthidae). Bull Mus Natl Hist Nat (Paris). 1984;6(A2):349–60.

    Google Scholar 

  68. Lourenço WR, Maury EA. Contribution a la connaissance systématique des scorpions appartenant au "complexe" Tityus bolivianus Kraepelin, 1895 (Scorpiones, Buthidae). Rev Arachnol. 1985;6(3):107–16.

    Google Scholar 

  69. Lourenço WR. Synopsis of the Colombian species of Tityus Koch (Chelicerata, Scorpiones, Buthidae), with descriptions of three new species. J Nat Hist. 2000;34:449–61.

    Article  Google Scholar 

  70. Lourenço WR. Tityus gasci, nouvelle espéce de scorpion Buthidae de Guyane française. Bull Mus NatL Hist Nat (Paris). 1981;4(A3):841–5.

    Google Scholar 

  71. Flórez E. Escorpiones de la familia Buthidae (Chelicerata: Scorpiones) de Colombia. B Colombiana. 2001;2(1):25–30.

    Google Scholar 

  72. Maury EA, Lourenço WR. Tityus roigi, nouvelle espéce de scorpion de l´Equateur (Scorpiones, Buthidae). Rev Arachnol. 1987;7(2):79–84.

    Google Scholar 

  73. Maury EA. Lista de los ejemplares típicos de "Arachnida" (Opiliones, Scorpiones y Solifugae) depositados en le Museo Argentino de Ciencias Naturales "Bernardino Rivadavia". Suplemento I. Aracnologia (Montevideo). 1992;6:1–10.

    Google Scholar 

  74. Pocock RI. Report upon the scorpiones and Pedipalpi obtained on the Lower Amazons by Messrs E.E. Austen and F. Pickard Cambridge during the trip of Mr. Siemen’s Steamship ´Faraday´. Ann Mag Nat Hist. 1897;19:357–68.

    Article  Google Scholar 

  75. Lourenço WR. Biogéographie des espéces du groupe naturel "Tityus clathratus" (Chelicerata, Scorpiones, Buthidae). Bull Mus Natl Hist Nat, (Paris). 1992;14(2):473–81.

    Google Scholar 

  76. Kovařík F, Stahlavsky F, Korinkova T, Kral J, van der Ende T. Tityus ythieri Lourenço, 2007 is a synonym of Tityus magnimanus Pocock, 1897 (Scorpiones: Buthidae): a combined approach using morphology, hybridization experiments, chromosomes, and mitochondrial DNA. Euscorpius. 2009;77:1–12.

    Google Scholar 

  77. Lourenço WR. Tityus (Atreus) timendus Pocock, 1898 (Scorpiones, Buthidae), an enigmatic scorpion from Ecuador. Acta Biol Paranaense. 2012;41(1–2):1–8.

    Google Scholar 

  78. Otero R, Navío E, Céspedes FA, Nuñez MJ, Lozano L, Moscoso ER, et al. Scorpion envenoming in two regions of Colombia: clinical, epidemiological and therapeutic aspects. Trans R Soc Trop Med Hyg. 2004;98(12):742–50.

  79. Rojas-Runjaic FJM, de Sousa L. Catálogo de los escorpiones de Venezuela (Arachnida: Scorpiones). Bol Soc Entomol Aragonesa. 2009;40:281–307.

    Google Scholar 

  80. Ythier E. Additional biological data on Tityus ythieri Lourenço, 2007. Bull Arthrop. 2011;44:3–7.

    Google Scholar 

  81. Ochoa JA, Prendini L. The genus Hadruroides Pocock, 1893 (Scorpiones: Iuridae), in Peru: new records and descriptions of six new species. Am Mus. 2010;3687:1–56.

    Article  Google Scholar 

  82. Maury EA. Escorpiones y escorpionismo en el Peru. IV: Revisión del género Hadruroides Pocock, 1893. Rev Peru Entomol. 1974;17(1):9–21.

    Google Scholar 

  83. Costal-Oliveira F, Duarte CG, Machado De Avila RA, Melo MM, Bordon KC, Arantes EC, et al. General biochemical and immunological characteristics of the venom from Peruvian scorpion Hadruroides lunatus. Toxicon. 2012;60(5):934–42.

    Article  CAS  PubMed  Google Scholar 

  84. Zuñiga Julca E, Vargas Chávez K, Díaz DV, Mercedes YV, Germán EV, Pereyra JV, et al. Efecto del veneno de Hadruroides charcasus sobre el tejido cardiaco de Bufo spinulosus. Rev Pharmaciencia. 2014;2(1):32–8.

    Google Scholar 

  85. Lubin YD. Changes in the native fauna of the Galápagos Islands following invasion by the little red fire ant. Wasmannia auropunctata Biol J Linn Soc. 1984;21:229–42.

    Article  Google Scholar 

  86. Baert LL. CDF checklist of Galapagos arachnids. In: Bungartz F, Herrera H, Jaramillo P, Tirado N, Jímenez-Uzcategui G, Ruiz D, editors. Charles Darwin Foundation Galapagos species checklist. Puerto Ayora, Galápagos: Charles Darwin Foundation; 2011. Accessed November 4, 2014.

    Google Scholar 

  87. Thorell T. Études scorpiologiques. Atti Soc It Sci Nat. 1876;19:75–272.

    Google Scholar 

  88. Carvajal V. Lista preliminar de artrópodos del Bosque Protector Pichincha y sus alrededores. Politécnica. 2005;26(1):141–60.

    Google Scholar 

  89. Patzelt E. Subphylum: Quelicerados. Classe Arachnida. In: Fauna del Ecuador. Quito: Banco Central del Ecuador; 1989. p. 392–9.

    Google Scholar 

  90. Festa E. Viaggio del Dr. Enrico Festa nel Darén, nell´Ecuador e regione vicine. Boll Mus Zool Anat Comp Reale Univ Torino. 1903;XVIII(435):1–9.

    Google Scholar 

  91. Lourenço WR. Resultados faunísticos de diversas campanas realizadas en America Latina; IV. Estudo de uma pequena coleçao de escorpioes do Peru e Equador, com a redescriçao de Tityus ecuadorensis Kraepelin, 1896. Speleon. 1983;26–27:11–5.

    Google Scholar 

  92. Botero-Trujillo R, Francke O. A new species of troglomorphic leaf litter scorpion from Colombia belonging to the genus Troglotayosicus (Scorpiones: Troglotayosicidae). Texas Memorial Museum Speleological Monographs, 7. Studies on the cave and endogean fauna of North America. 2009. p. 1–10.

    Google Scholar 

  93. Pardal PP, Ishikawa EA, Vieira JL, Coelho JS, Dórea RC, Abati PA, et al. Clinical aspects of envenomation caused by Tityus obscurus (Gervais, 1843) in two distinct regions of Para state, Brazilian Amazon basin: a prospective case series. J Venom Anim Toxins incl Trop Dis. 2014;20(1):3.

    Article  PubMed Central  PubMed  Google Scholar 

  94. Lourenço WR. The distribution of noxious species of scorpions in Brazilian Amazonia: the genus Tityus C. L. Koch, 1836, subgenus Atreus gervais, 1843 (Scorpiones, Buthidae). Entomol Mitt Zool Mus Hamburg. 2011;15(185):287–301.

    Google Scholar 

  95. Lourenço WR. Synopsis de la faune de scorpions de Colombie, avec des considérations sur le systématique et la biogeographie des espéces. Rev Suisse Zool. 1997;104(1):61–94.

    Google Scholar 

  96. Gentry AH. Tropical forest biodiversity: distributional patterns and their conservational significance. Oikos. 1992;63(1):19–28.

    Article  Google Scholar 

  97. Skog LE, Kvist LP. Revision of Gasteranthus (Gesneriaceae). Syst Bot Monogr. 2000;59:1–118.

    Article  Google Scholar 

  98. Vargas JH, Consiglio T, Jorgensen PM, Croat TB. Modelling distribution patterns in a species-rich plant genus, Anthurium (Araceae), in Ecuador. Div Distrib. 2004;10:211–6.

    Article  Google Scholar 

  99. Wolf T. Geografía y geología del Ecuador. Leipzig: Tipografía de F.A. Brockhaus; 1892.

    Google Scholar 

  100. Zavaleta A, Navarro J, Castro de la Mata R. Pharmacological action of a peruvian scorpion (Hadruroides lunatus) venom. Toxicon. 1981;19:906–9.

    Article  CAS  PubMed  Google Scholar 

  101. Armas LF, Luna-Sarmiento D, Flórez E. Composición del género Centruroides Marx, 1890 (Scorpiones: Buthidae) en Colombia, con la descripción de una nueva especie. Bol Soc Entomol Aragonesa. 2012;50:105–14.

    Google Scholar 

  102. Borges A, Jowers MJ, Bónoli S, de Sousa L. Scorpions from the primeval subgenus Archaeotityus produce putative homologs of Tityus serrulatus toxins active on voltage-gated sodium channels. J Venom Anim Toxins incl Trop Dis. 2012;18(4):432–40.

    Article  Google Scholar 

  103. Nicholls H. The Galápagos: a natural history. New York: Basic books; 2014.

    Google Scholar 

  104. Dupérré N. Demystifying three species of Ctenidae (Arachnida: Araneae) described by Embrik Strand. Part I, Ecuador. Zootaxa. 2014;3784(1):67–73.

    Article  PubMed  Google Scholar 

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The Secretaría Nacional de Educación Superior, Ciencia, Tecnología e Innovación (Ecuador) is gratefully acknowledged for its financial support through the program Prometeo (to A.B.). We would also like to thank Dr. Carmen Bonifaz de Elao, Faculty of Natural Sciences, Universidad de Guayaquil, for her constant support and help with logistics during collection work. Thanks are conveyed to Dr. Jorge Blanco, from Fundación Herpetológica Gustavo Orcés, Quito, Ecuador, for informing us on the severe and fatal scorpion stings in children he witnessed in the province of Morona Santiago. We are grateful to Xavier Cornejo, Michiel Cozijn, Radomir Jirsak, Jan Ove Rein, Tatiana Torres, David Reyes, Richard C. West, and Eric Ythier for allowing us to use their photographs. Dr. Clifford Keil, Director, Invertebrate Museum, Pontificia Universidad Católica del Ecuador, Quito, kindly allowed us to examine and photograph the specimen of Teuthraustes atramentarius appearing in this publication. We thank Dr. Andrea Rossi for confirming the identity of the H. charcasus specimen appearing in Fig. 4. Dr. Telmo Ariel Escobar, Biol. Jaime Santos, and Biol. José David Villalta, from the Faculty of Natural Sciences, Universidad de Guayaquil, are acknowledged for their support during collections and data gathering. We are extremely thankful to Dr. Miguel Delgado, for his persistent support, great spirit and humor, and for sharing with us his unpublished observations on envenoming by Centruroides margaritatus in Guayaquil.

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GB gathered data compiled in Fig. 1, contributed with bibliography and revised the final draft. AB wrote the manuscript and prepared Figs. 2, 3 and 4. Both authors read and approved the final manuscript.

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Brito, G., Borges, A. A checklist of the scorpions of Ecuador (Arachnida: Scorpiones), with notes on the distribution and medical significance of some species. J Venom Anim Toxins Incl Trop Dis 21, 23 (2015).

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