REVSYS: SYSTEMATICS OF THE
SCORPION FAMILY VAEJOVIDAE
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What are vaejovids?

Family Vaejovidae
Genus Paravaejovis

Genus Paruroctonus
Genus Pseudouroctonus
Genus Serradigitus
Genus Smeringurus
Genus Syntropis
Genus Uroctonites
Genus Uroctonus
Genus Vaejovis
Genus Vejovoidus

Why study vaejovids?

Diversity
Endemism
Taxonomy
Phylogeny
Biogeography

Bibliography

Genus Paruroctonus Werner 1934

Synonymy

Paruroctonus Werner, 1934 (January?): 283, fig. 363; type species by monotypy Uroctonoides gracilior Hoffmann, 1931 [=Paruroctonus gracilior (Hoffmann, 1931)]. 

SYNONYMS:

Uroctonoides Hoffmann, 1931: 405, fig. 42; type species by monotypy Uroctonoides gracilior Hoffmann, 1931 [=Paruroctonus gracilior (Hoffmann, 1931)]; preoccupied as Uroctonoides Chamberlin, 1920 (=Teuthraustes Simon, 1878) (synonymized by Werner, 1934: 283).

Hoffmanniellius Mello-Leitão, 1934a (June 30): 80 (proposed replacement name for Uroctonoides Hoffmann); type species Uroctonoides gracilior Hoffmann, 1931 [=Paruroctonus gracilior (Hoffmann, 1931)] [synonymized by Stahnke, 1957: 253 (in footnote)].

 REFERENCES:

Paruroctonus: Kästner, 1941: 237; Stanhke, 1957: 253 (part); Stahnke, 1965: 262, 263 (part); Bücherl, 1971: 329; Williams, 1972: 1-3 (part; reinstated as genus); Soleglad, 1972a: 71-75 (part); Soleglad, 1973b: 353, 355 (part); Williams, 1974: 15 (part); Stahnke, 1974a: 119, 136, fig. 10; Vachon, 1974: 914, 916; Williams, 1980: 31-34, fig. 35-37 (part); Francke & Soleglad, 1981: 241, 243 (part); Sissom & Francke, 1981: 93 (part); Francke, 1985: 11, 18, 21; Sissom & Francke, 1985: 264 (part); Sissom, 1990a: 110, 114 (part); Stockwell, 1992: 408, 409, 416, 419, fig. 12, 37, 39, 58; Sissom et al., 1998: 17-19; Kovarík, 1998: 143; ICZN, 1999: 209-210; Beutelspacher, 2000: 56, 65, 152; Sissom, 2000:505-506; Soleglad & Fet, 2003a: 15, 31, 33, 36, 67, 140, 142, 163, 164, figs. 66, 79, 80, 111, D-5, Tabs. 3, 4, 9.

Hoffmanniellus (ISS): Mello-Leitão, 1945: 118; Vachon, 1963a: 163.

Vejovis (Paruroctonus): Gertsch & Allred, 1965: 4 (part); Gertsch & Soleglad, 1966: 3-7 (part); Gertsch & Soleglad, 1972: 553, 559 (part); Williams & Hadley, 1967: 112 (part); Williams, 1968a: 7 (part); Williams, 1970b: 277 (part).

Vaejovis (Paruroctonus): Hjelle, 1972: 26 (part).

Vaejovis: Díaz Najera, 1975: 3, 6 (part).

Paruroctonus (Paruroctonus): Haradon, 1983: 256; Haradon, 1984a: 205-209; Haradon, 1984b: 317-318; Haradon, 1985: 19-21.

Description.  

Prosoma. –  Anterior carapacial margin straight to convex.

Mesosoma. – Pectinal tooth counts 13-39 in males, 8-24 in females. All female pectinal teeth similar in size and shape, and with sensorial areas. 

Metasoma. –  Dorsal carinae of segments I-IV with even granulation, rounded off distally.  Ventral submedian carinae of segments I-IV paired and variously developed, ranging from absent (usually on proximal segments) to granular to denticulate (strength and granulation usually increasing posteriorly).  Ventral intercarinal spaces lacking accessory setae.  Segment V with linear ventromedian carina (i.e., not bifurcated distally).

Chelicerae. –  Ventral margin of the cheliceral movable finger with or without denticles or crenulations; fixed finger lacking ventral denticles.  Serrula of movable finger absent.

Pedipalps. – Patella:  Inner face with basal tubercles moderately developed; inner longitudinal carina present, usually consisting of several granules.  Chelal carinae:  Carinal development variable, some with all carinae developed and granular to denticulate, others with various carinae reduced; sexual dimorphism prominent (females often with reduced carination). Chela dentition: Terminal denticles moderately large, conically shaped.  Chela fixed finger with primary denticle row divided into six subrows of denticles, these are flanked by six inner accessory denticles.   Chela movable finger with primary denticle row divided into six to seven subrows of denticles, these flanked by seven inner accessory denticles. Denticles of denticle row subconical, rounded to more narrow, subserrate.

Trichobothrial Pattern. –  Patella with two ventral trichobothria along ventroexternal carina (the third ventral trichobothrium is positioned on the external face). Chela with four ventral (V) trichobothria.  Chelal trichobothria ib positioned at base of fixed finger or displaced slightly from base.  Chela finger trichobothrium est about equidistant between et and esb.

Legs. –  Basitarsi and often telotarsi with setal combs.  Telotarsi ventrally with a median row of small spinules that are flanked distally by one pair of slightly larger spinules.  Ventromedian spinule row flanked laterally by setae.

Hemispermatophore. – No published observations exist.

Included groups. – gracilior, boreus, and stahnkei infragroups.

Similar taxa. – See Vejovoidus Stahnke, Paravaejovis Williams, and Smeringurus Haradon.

 Remarks. - Haradon (1983, 1984a, 1984b, 1985) revised this genus and divided it into two subgenera, Paruroctonus and Smeringurus. Haradon (1984a, 1984b, 1985) further divided subgenus Paruroctonus into a number of presumably monophyletic groupings. Larger groups were referred to as infragroups (gracilior infragroup, boreus infragroup, stahnkei infragroup), for which a key was provided by Haradon (1985), and two of these were subdivided into microgroups.  The boreus infragroup includes the boreus, becki, xanthus, and baergi microgroups, and the stahkei infragroup includes the stahnkei, shulovi, borregoensis, and williamsi microgroups.  Stockwell (1992) elevated Smeringurus to genus, but it is doubtful whether either Smeringurus or Paruroctonus is monophyletic (although the group comprising Paravaejovis, Paruroctonus, Smeringurus and Vejovoidus probably is). Paruroctonus thus currently includes 29 species and 4 subspecies, all fossorial and most psammophilous, inhabiting sand dune systems throughout the deserts of the western USA and northwestern Mexico. Some, e.g. P. gracilior, prefer packed sandy soils and even rocky or gravelly habitats. The dune systems of Chihuahua and Coahuila have not been well sampled and new Paruroctonus species may occur there.

 Literature Cited.

Haradon, R.M. 1983. Smeringurus, a new subgenus of Paruroctonus Werner (Scorpiones, Vaejovidae). Journal of Arachnology 11: 251–270.

Haradon, R.M. 1984a. New and redefined species belonging to the Paruroctonus borregoensis group (Scorpiones, Vaejovidae). Journal of Arachnology 12: 317–339.

Haradon, R.M. 1984b. New and redefined species belonging to the Paruroctonus baergi group (Scorpiones, Vaejovidae). Journal of Arachnology 12: 205–221.

Haradon, R.M. 1985. New groups and species belonging to the nominate subgenus Paruroctonus (Scorpiones, Vaejovidae). Journal of Arachnology 13: 19–42.

Stockwell, S.A. 1992. Systematic observations on North American Scorpionida with a key and checklist of the families and genera. Journal of Medical Entomology 29: 407–422.

 


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