Published September 24, 2021 | Version v1
Taxonomic treatment Open

Charinus brasilianus Weygoldt 1972

  • 1. Center for Macroecology, Evolution and Climate, Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark. & Entomology Department, National Museum of Natural History, Smithsonian Institution, Washington DC, USA.
  • 2. Laboratório de Referência Nacional em Vetores das Riquetsioses, LIRN-IOC-FIOCRUZ, Rio de Janeiro, RJ, Brazil.
  • 3. Arachnology Lab, Division of Invertebrate Zoology, American Museum of Natural History, New York, NY, USA.
  • 4. Center for Macroecology, Evolution and Climate, Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark. & Entomology Department, National Museum of Natural History, Smithsonian Institution, Washington DC, USA. & Zoology Section, Natural History Museum of Denmark, University of Copenhagen, Denmark.

Description

Charinus brasilianus Weygoldt, 1972

Figs 8C–D, 43, 48; Table 4

Charinus brasilianus Weygoldt, 1972b: 108–115, figs 1–11, 22a.

Charinus brasilianus – Weygoldt 1972c: 100, fig. 7a–b; 1972d: 37–40, figs 8–9, 10a–b; 1975: 311; 1996a: 187, 189–190, figs 2, 13–14, 22, 40; 1999b: 52, fig. 6; 1999c: 107, figs 8–10; 2000a: 15, 17, 75, 98, figs 6–9, 15, 152–153, 212; 2000b figs 348, 4–5; 2006a: 239–240, 245–246, fig. 13. — Weygoldt et al. 1972: 209–246, figs 14d, 16b, 18c, 19. — Delle Cave 1986: 162, fig. II. — Proctor 1998: 160. — Harvey 2003: 4–5. — Baptista & Giupponi 2003: 80. — Haupt 2009: 18, fig. 4. — Miranda & Giupponi 2011: 66, fig. 13. — Jocqué & Giupponi 2012: 59. — Vasconcelos et al. 2013: 495, fig. 12. — Vasconcelos & Ferreira 2016: 185. — Miranda et al. 2016c: 19, 21, 29, 31.

Diagnosis

This species may be separated from C. monasticus sp. nov., C. taboa, C. troglobius, and C. una sp. nov. by the presence of well-developed median and lateral eyes. It differs from C. diamantinus sp. nov., C. euclidesi sp. nov., C. souzai, and C. sooretama sp. nov., in the lower number of teeth on the cheliceral claw: six teeth are present in C. brasilianus whereas more than six are present in the other species.

Etymology

Although unspecified, the species name is evidently an adjective referring to Brazil, the country in which the type locality is located.

Type material

Holotype BRAZIL • ♂; Espírito Santo, 10 km N of Vitoria; [20°11′08.74″ S, 40°16′05.53″ W]; “Berg links d. Strass u. Nova Almeida”; Weygoldt leg.; Oct. 1970; MNRJ 9014.

Paratypes BRAZIL • 1 ♀; same collection data as for holotype; MNRJ 9014 • 1 ♀, 3 juv. ♂♂, 3 ♂♂, 2 juv. [without gonopod]; same collection data as for holotype; SMF 25397.

Additional material

BRAZIL • 1 ♀, 1 ♂; Espírito Santo, Santa Tereza, Nova Valssugana; May 2005; T. Souza leg., MNRJ 9271 • 1 juv. ♀; Espírito Santo, Santa Tereza, Reserva Santa Lúcia; 19°56′10″ S, 40°36′06″ W; 15–19 Oct. 2003; Almeida, Bapstista, Giupponi, Mendes and Pedroso leg.; MNRJ 9232 • 2 ♀♀, 3 ♂♂, 3 juv.; Espírito Santo, Aracruz, Parque Natural Municipal do Aricanga; 19°49′07.21″ S, 40°19′47.57″ W; 17 Oct. 2005; MNRJ 9240 • 2 ♀♀, 1 juv. ♂; Espírito Santo, Aracruz, Aricanga; MNRJ 9233 • 1 ♂; Espírito Santo, Aracruz, REFMU do Aricanga; 14 Oct. 2005; Expedição ESFA leg.; MNRJ 9241 • 1 ♀, 4 ♂♂; Espírito Santo, Aracruz, Parque Natural Municipal David Victor Farina; 19°55′55.67″ S, 40°07′39.22″ W; 15 Oct. 2005; A. Giupponi, A. Kury, V. Orrico, M. Milleri, R. Rodrigues and T. Souza leg.; MNRJ 9226.

Supplementary description

CARAPACE. Frontal process large, triangular, not visible in dorsal view; median eyes and median ocular tubercle present (Fig. 48A–B, G); lateral eyes well developed, small seta posterior to each lateral ocular triad; lenses directed anteriorly and dorsally.

STERNUM. Tritosternum projected anteriorly into large blunt tubercle; medial platelet (tetrasternum) and third platelet (pentasternum) with one convex platelet, with pair of setae anteriorly and few small setae posteriorly (Fig. 48H); metasternum with clear division in anterior half, and with anterior seta in membranous region and seta in sclerotized area, where sulcus terminates; anterior margin with small elevation bearing longitudinal row of five large setae with longitudinal series of smaller setae anterior to them.

OPISTHOSOMA. Ventral sacs and ventral sac cover absent.

GENITALIA. Female genital operculum posterior margin straight, with few setae along margin and on surface; gonopods sucker-like, with wrinkled, folded cushion basally. Male gonopods with fimbriate LoL2, separated from LoL1 (Fig. 8C–D).

CHELICERAE. Prolateral surface of basal article with vertical row of three or four setae; claw with six or seven teeth.

PEDIPALPS. Femur with four (males) or five (females) dorsal spines and two prominent setiferous tubercles proximal to spine 1 (Fig. 48C, E); four or five ventral spines with one setiferous tubercle proximal to spine 1 and small spine displaced from primary series dorsal to spine 1 (Fig. 48D, F). Patella with five dorsal spines; spine distal to spine 1, about one-third length of spine 1 (Fig. 48C, E); three or four conspicuous ventral spines, decreasing in size, with small setiferous tubercles and spines forming secondary series between primary series of spines (Fig. 48D, F). Tibia with two dorsal spines; ventral spine situated in distal half, two-thirds length of proximal dorsal spine; two setae between spine and distal margin. Tarsus with two small curved spines, distal spine one-fifth length of tarsus, and proximal spine half length of distal spine. Ventral row of cleaning brush organ with 25–29 setae.

LEGS. Tibia of leg I with 23 or more articles (one specimen with 27 articles, another with 31); tarsus I with 41 or more articles (one specimen with 44 articles, another with 43); first (distal) article of tibia with two small trichobothria, second article with one, third article with two, and fourth article with one. Leg IV basitibia with four pseudo-articles, with trichobothrium situated at distal end of first half of last pseudo-article; distitibia trichobothrium bc situated closer to sbf than to bf; sc and sf series each with five trichobothria.

Measurements

See Table 4.

Distribution

Populations of C. brasilianus were collected in several different municipalities, e.g., Aracruz, Aricanga, and Santa Teresa, in the vicinity of the type locality.

Natural history

This species occurs under stones and fallen tree trunks in tropical forest.

Notes

Published as part of Miranda, Gustavo Silva de, Giupponi, Alessandro P. L., Prendini, Lorenzo & Scharff, Nikolaj, 2021, Systematic revision of the pantropical whip spider family Charinidae Quintero, 1986 (Arachnida, Amblypygi), pp. 1-409 in European Journal of Taxonomy 772 on pages 98-100, DOI: 10.5852/ejt.2021.772.1505, http://zenodo.org/record/5536410

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Linked records

Additional details

Biodiversity

References

  • Weygoldt P. 1972 a. Charinus koepckei n. sp. aus Peru (Amblypygi: Charontidae). Senckenbergiana Biologica 53: 281 - 286.
  • Weygoldt P. 1972 b. Charontidae (Amblypygi) aus Brasilien. Zoologische Jahrbucher, Abteilung fur Systematik, Okologie und Geographie der Tiere 99: 107 - 132.
  • Weygoldt P. 1972 c. Geisselskorpione und Geisselspinnen (Uropygi und Amblypygi). Zeitschrift des Kolner Zoo 15: 95 - 107.
  • Weygoldt P., Weisemann A. & Weisemann K. 1972. Morphologisch-histologische Untersuchungen an den Geschlechtsorganen der Amblypygi unter besonderer Berucksichtigung von Tarantula marginemaculata C. L. Koch (Arachnida). Zeitschrift fur Morphologie und Okologie der Tiere 73: 209 - 247. https: // doi. org / 10.1007 / BF 00297206
  • Delle Cave L. 1986. Biospeleology of the Somaliland Amblypygi (Arachnida, Chelicerata) of the caves of the Showli Berdi and Mugdile (Bardera, Somaliland). Redia 69: 143 - 170.
  • Proctor H. C. 1998. Indirect sperm transfer in arthropods: Behavioral and evolutionary trends. Annual Review of Entomology 43: 153 - 174. https: // doi. org / 10.1146 / annurev. ento. 43.1.153
  • Harvey M. S. 2003. Catalogue of the Smaller Arachnid Orders of the World. Amblypygi, Uropygi, Schizomida, Palpigradi, Ricinulei and Solifugae. CSIRO Publishing, Collingwood, Australia. https: // doi. org / 10.1071 / 9780643090071
  • Baptista R. L. C. & Giupponi A. P. L. 2003. A new troglomorphic Charinus from Minas Gerais State, Brazil (Arachnida: Amblypygi: Charinidae). Revista Iberica de Aracnologia 7: 79 - 84.
  • Haupt J. 2009. Chelicerae of arachnids: Facts and fiction. Arthropoda Selecta 18: 17 - 19.
  • Miranda G. S. & Giupponi A. P. L. 2011. A new synanthropic species of Charinus Simon, 1892 from Brazilian Amazonia and notes on the genus (Arachnida: Amblypygi: Charinidae). Zootaxa 2980: 61 - 68. https: // doi. org / 10.11646 / zootaxa. 2980.1.5
  • Jocque M. & Giupponi A. P. L. 2012. Charinus bromeliaea sp. n. (Amblypygi: Charinidae); a new species of bromeliad inhabiting whip spider from French Guyana. Zootaxa 3158 (2): 53 - 59. https: // doi. org / 10.11646 / zootaxa. 3158.1.4
  • Vasconcelos A. C., Giupponi A. P. L. & Ferreira R. L. 2013. A new species of Charinus Simon, 1892 from northeastern Brazil with comments on the potential distribution of the genus in Central and South Americas (Arachnida: Amblypygi: Charinidae). Zootaxa 3737: 488 - 500. https: // doi. org / 10.11646 / zootaxa. 3737.4.9
  • Vasconcelos A. C. O. & Ferreira R. L. 2016. Description of two new species of Charinus Simon, 1892 from Brazilian caves with remarks on conservation (Arachnida: Amblypygi: Charinidae). Zootaxa 4072 (2): 185 - 202. https: // doi. org / 10.11646 / zootaxa. 4072.2.3
  • Miranda G. S., Milleri-Pinto M., Goncalves-Souza T., Giupponi A. P. L. & Scharff N. 2016 c. A new species of Charinus Simon, 1892 (Amblypygi, Charinidae) from Brazil, with notes on behavior. ZooKeys 621: 15 - 36. https: // doi. org / 10.3897 / zookeys. 621.9980