Vizcaino, González-Santillán & Prendini, 2013
publication ID |
https://doi.org/ 10.1206/830.1 |
DOI |
https://doi.org/10.5281/zenodo.4627449 |
persistent identifier |
https://treatment.plazi.org/id/174CE445-FFC4-2E68-0B20-9BED91F1FA41 |
treatment provided by |
Felipe |
scientific name |
Vizcaino |
status |
gen. nov. |
Vizcaino View in CoL , gen. nov.
Figures 1F View Fig , 6 View Fig , 7 View Fig , 20C View Fig , 21C View Fig ; table 1 View TABLE 1
Vejovis viscainensis Williams, 1970 [= Vizcaino viscainensis (Williams, 1970) View in CoL , comb. nov.], type species, by monotypy.
Vaejovis eusthenura group (part): Williams, 1980: 55; Sissom, 1991: 26; Stockwell, 1992: 408, 409; Sissom, 1993: 68; Lourenço and Sissom, 2000: 135; Sissom, 2000: 530, 532, 551; Armas and Martín-Frías, 2001: 8; González-Santillán, 2004: 29; Ponce-Saavedra and Sissom, 2004: 541; Francke and Ponce-Saavedra, 2005: 67; Sissom and Hendrixson, 2005b: 33, 34; Fet et al., 2006a: 7; 2006b: tables 1 View TABLE 1 , 9; Graham and Soleglad, 2007: 9, 11, 12; Soleglad et al., 2007: 134, 135; McWest, 2009: 8, 48, 52, 56, 61, 64, 98, 101–103, 108, table 1 View TABLE 1 ; Santibáñez-López and Sissom, 2010: 49.
Hoffmannius (part): Soleglad and Fet, 2008: 1 View Cited Treatment , 26, 57, 60, 89, 91, 96, 102; Ayrey and Soleglad, 2011: 1.
ETYMOLOGY: The generic name is a noun in apposition, masculine in gender, taken from the Vizcaino Desert in the Baja California Peninsula, to which this monotypic genus is endemic.
DIAGNOSIS: Vizcaino , gen. nov., is unique among Syntropinae in possessing four primary subrows of median denticles, separated by five retrolateral denticles, in the median denticle row of the pedipalp movable finger (fig. 20C); the terminal subrow, comprising one to three denticles in the other genera of Syntropinae , is absent (figs. 17A, C, 18A, 19A, C, 20A–C). The following combination of characters is also unique for the genus: pedipalp femur, rlv carina smooth and costate; legs I–III, basitarsi (male and female) laterally compressed, each with dorsal and retrodorsal macrosetae elongated and arranged into a sublinear row, forming a setal comb (fig. 21C); legs I–IV, telotarsi each with basal, ventromedian and distal series of spinules slender and elongate (fig. 21C); metasomal segments I–IV, vsm carinae distinct (protruding above adjacent intercarinal surfaces) and finely denticulate.
Vizcaino , gen. nov., appears superficially similar to some species of Chihuahuanus , gen. nov., and Paravaejovis (e.g., C. globosus , comb. nov., P. pumilis , and, to a lesser extent, other species of Paravaejovis in the Baja California Peninsula) with which it shares setal combs on the basitarsi of legs I–III (fig. 21C). In addition to the abovementioned characters, Vizcaino , gen. nov., differs from these taxa by possessing elongated pedipalp chela fingers, such that trichobothrium eb is situated on the fixed finger between RD6 and RD7, it is situated on the fixed finger between PD5 and PD6, and ib is situated on the fixed finger, at or close to PD6. Trichobothrium eb is situated at RD7, it at PD6 and ib between PD6 and PD 7 in Chihuahuanus , gen. nov., and most species of Paravaejovis , except P. confusus , comb. nov., and related species in which the positions of these trichobothria are similar to those of Vizcaino , gen. nov. Paravaejovis confusus , comb. nov., and related species are readily distinguished from Vizcaino , gen. nov., by the dentition of the pedipalp chela movable finger, and the telotarsal spinules.
Vizcaino , gen. nov., shares with Konetontli , gen. nov., Kuarapu , Maaykuyak , gen. nov., Syntropis , Chihuahuanus bilineatus , comb. nov., C. coahuilae , comb. nov., and Thorellius cristimanus the presence of a secondary hook on the hemispermatophore (fig. 8H), created by an extension of the axial carina of the distal lamina, that forms a pronounced bifurcation with the primary hook.
INCLUDED SPECIES: Vizcaino viscainensis (Williams, 1970) , comb. nov.
DISTRIBUTION: Vizcaino , gen. nov., is endemic to the Vizcaino Desert of the Baja California Peninsula, Mexico, and recorded from the states of Baja California and Baja California Sur (fig. 6).
NATURAL HISTORY: According to Williams (1970b), this species is rarely collected, and may have limited surface activity, spending most of its life inside burrows. The known specimens were collected at night with UV light detection on sparsely vegetated, semistabilized sand dunes, from sea level to 262 m altitude. This species appears to be more abundant in areas where coastal fog is frequent. The habitat and habitus, especially the setal combs and elongated spinules on the leg tarsi, and the pale, immaculate integument are consistent with the psammophilous ecomorphotype ( Prendini, 2001a).
REMARKS: Williams (1980) originally placed this species in the eusthenura group of Vaejovis , for which Soleglad and Fet (2008) devised the name Hoffmannius , without quantitatively testing either its monophyly or composition. Hoffmannius , as defined by Soleglad and Fet (2008), was consistently polyphyletic in the phylogenetic analyses by González-Santillán and Prendini (in press). Vizcaino , gen. nov., was not related to the species assigned to Hoffmannius by Soleglad and Fet (2008), forming a monophyletic group with Syntropis instead (fig. 7). The creation of a monotypic genus for this species is based on its phylogenetic position and unique, diagnostic character combination.
MATERIAL EXAMINED: Vizcaino viscainensis (Williams, 1970) , comb. nov.: MEXICO: Baja California: Municipio de Ensenada: Miller’s Landing, 2 mi. NW, 25 ft, 21.vi.1968, S.C. Williams and M.A. Cazier, holotype ♂ of V. viscainensis ( CAS Type No. 10429). Baja California Sur: Municipio de Mulegé: Las Bombas, 3.2 km E, 30 m, 16.iv.1969, S.C. Williams, 2♀ ( AMNH); Sierra del Placer, 21 km to junction Bahía Tortugas and Bahía Asunción, 98 km E of Vizcaino towards Bahía Tortugas, 27 ° 28.9278 ′ N 114 ° 17.0928 ′ W, 262 m, 28.vi.2008, H. Montaño and E. González, 88, 6♀, 13 juv. ( AMNH [ ARA 2855 ]), GoogleMaps 88, 6♀ ( IBUNAM [ARA 2245]).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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SubFamily |
Syntropinae |
Vizcaino
González-Santillán, Edmundo & Prendini, Lorenzo 2013 |
Vaejovis eusthenura
Santibanez-Lopez, C. & W. D. Sissom 2010: 49 |
McWest, K. J. 2009: 8 |
Graham, M. R. & M. E. Soleglad 2007: 9 |
Soleglad, M. E. & G. Lowe & V. Fet 2007: 134 |
Fet, V., M. E. & M. S. Brewer 2006: 7 |
Francke, O. F. & J. Ponce-Saavedra 2005: 67 |
Sissom, W. D. & B. E. Hendrixson 2005: 33 |
Gonzalez-Santillan, E. 2004: 29 |
Ponce-Saavedra, J. & W. D. Sissom 2004: 541 |
Armas, L. F. de & E. Martin-Frias 2001: 8 |
Lourenco, W. R. & W. D. Sissom 2000: 135 |
Sissom, W. D. 2000: 530 |
Sissom, W. D. 1993: 68 |
Stockwell, S. A. 1992: 408 |
Sissom, W. D. 1991: 26 |
Williams, S. C. 1980: 55 |