Charinus bahoruco Teruel, 2016
publication ID |
https://doi.org/ 10.5852/ejt.2021.772.1505 |
publication LSID |
lsid:zoobank.org:pub:9B82A32F-0A07-47E3-8684-FED7C8EBF1E9 |
DOI |
https://doi.org/10.5281/zenodo.5573033 |
persistent identifier |
https://treatment.plazi.org/id/8F431375-FF96-FFC0-A546-FDCDFB03DE75 |
treatment provided by |
Felipe |
scientific name |
Charinus bahoruco Teruel, 2016 |
status |
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Charinus bahoruco Teruel, 2016 View in CoL
Fig. 12 View Fig ; Table 1 View Table 1
Charinus bahoruco Teruel, 2016: 7–8 View in CoL , figs 4–6, 7b, 8.
Charinus sp. – Armas & Pérez, 2001: 50, 59, 64, figs 2a, c, e, 11. — Armas 2004: 39; 2006b: 229, 242.
Diagnosis
Based on the description of Teruel (2016), this species may be separated from other Caribbean and Central American Charinus by means of the following combination of characters: median eyes absent, median ocular tubercle small; lateral eyes well developed; tritosternum very short (slightly longer than wide); cheliceral basal segment with retrolateral tooth reduced to vestigial boss; cheliceral claw with four or five teeth; pedipalp femur with three dorsal spines and three ventral spines; pedipalp patella with three dorsal spines and two ventral spines; pedipalp tarsus with two dorsal spines; tibia of leg I with 21 articles, tarsus I with 37 articles; leg IV basitibia with three pseudo-articles; secondary sexual dimorphism present, males larger than females.
This species resembles C. dominicanus , but may be differentiated by the number of articles on the tarsus of leg I, which comprises 37 articles in C. bahoruco but 33 in C. dominicanus . Additionally, C. dominicanus bears eight teeth on the cheliceral claw, whereas C. bahoruco bears four or five teeth. The count of 21 articles on tibia of leg I also differentiates C. bahoruco from C. acosta , C. belizensis , C. centralis , C. muchmorei , and C. reddelli , in which the tibia comprises 23 articles. Charinus bahoruco differs from C. acosta , C. aguayoi and C. bruneti in the absence of median eyes, and from C. caribensis in the count of three preudo-articles in basitibia of leg IV. The short tritosternum, which barely reaches base of pedipalp coxae, is a unique character this species shares with C. dominicanus .
Etymology
Noun in apposition referring to the name of the mountain range, Sierra de Bahoruco, where the type locality is located ( Teruel 2016).
Type material
Holotype DOMINICAN REPUBLIC • ♂; Pedernales Province, Pedernales Municipality, Sierra de Bahoruco , Sección Mencía , Banano , El Mulito [Río Mulito]; 18°09′34″ N, 71°44′56″ W; 12 Mar. 2014; 409 m a.s.l.; R. Teruel, F. Kovařík and P. Kindl leg.; BIOECO [not examined]. GoogleMaps
Paratypes DOMINICAN REPUBLIC • 7 ♀♀, 3 ♂♂, 1 juv.; same collection data as for holotype; BIOECO [not examined] GoogleMaps • 1 ♀, 1 ♂; same collection data as for holotype; IES [not examined] GoogleMaps .
Measurements
See Table 1 View Table 1 .
Distribution
Known only from the westernmost part of the southern watershed of the Sierra de Bahoruco range in the Dominican Republic. Hispaniola is the second largest Caribbean island and contains ten species of whip spiders on its 76 192 km ², four of which are endemic to the Dominican Republic, C. bahoruco , C. dominicanus , C. magua and Phrynus kennidae Armas & Perez Gonzalez, 2001 , the first two restricted to the Pedernales and Baharona Provinces, in and around the Sierra de Bahoruco.
Natural history
Specimens were found under rocks among leaf litter, close to streams, in a broadleaf semideciduous forest ( Teruel 2016). Specimens were always in small groups of two to four individuals.
Pedipalp | Leg IV | ||||||||||||||||||
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Species | Additional information | Source | Sex | Carapace length | Carapace width | Femur length | Patella length | Tibia length | Tarsus length | Claw length | Femur I length | Femur | Basitibia article I | Basitibia article II | Basitibia article III | Basitibia article IV | Distitibia | Basitarsus | Other tarsal articles |
C. acosta | Holotype | Quintero 1983 | ♀ | 2.10 | 2.90 | – | 1.50 | – | – | – | 4.50 | 2.80 | 4.60 | – | – | – | – | – | – |
C. acosta | Víquez et al. 2012 | ♀ | 2.40 | 3.10 | 5.60 | – | – | – | – | 4.80 | 3.20 | – | – | – | – | – | – | – | |
C. aguayoi | Holotype of C. victori | Armas 2010 | ♂ | 2.34 | 3.12 | 3.54 | 4.06 | 1.09 | 1.14 | – | 4.63 | 2.86 | – | – | – | – | – | – | – |
C. aguayoi | Paratopotype of C. victori | Armas 2010 | ♂ | 2.18 | 3.12 | 3.22 | 3.64 | 1.04 | 0.94 | – | 4.89 | 3.12 | – | – | – | – | – | – | – |
C. aguayoi | Paratopotype of C. victori | Armas 2010 | ♀ | 1.82 | 2.50 | 1.14 | 1.50 | 0.78 | 0.73 | – | 3.38 | 2.34 | – | – | – | – | – | – | – |
C. aguayoi | Río Abajo | Armas 2010 | ♂ | 1.87 | 2.70 | 1.87 | 2.44 | 0.83 | 0.94 | – | 3.64 | 2.50 | – | – | – | – | – | – | – |
C. aguayoi | Río Abajo | Armas 2010 | ♀ | 1.92 | 2.76 | 1.35 | 1.61 | 0.73 | 0.98 | 3.48 | 2.65 | – | – | – | – | – | – | – | |
C. aguayoi | USNM 782819 | This work | ♂ | 2.10 | 2.85 | 3.28 | 3.40 | 1.05 | 0.71 | 0.52 | 4.10 | 2.81 | 1.00 | 0.43 | 0.68 | – | 1.63 | 0.87 | 0.56 |
C. aguayoi | CAB IA 2 | This work | ♀ | 2.36 | 3.44 | 2.34 | 2.25 | 1.13 | 0.80 | 0.75 | 5.94 | 4.06 | 2.00 | 0.65 | 1.08 | – | 2.28 | 1.18 | 0.63 |
C. aguayoi | CAB B10AB | This work | ♀, juv | 1.88 | 2.59 | 1.33 | 1.18 | 0.69 | 0.54 | 0.43 | 3.31 | 2.34 | 1.00 | 0.32 | 0.52 | – | 1.28 | 0.70 | 0.50 |
C. aguayoi | USNM 392752 | This work | ♀, with eggs | 2.16 | 3.08 | 1.94 | 1.88 | 1.03 | 0.63 | 0.64 | 4.50 | 2.88 | 1.32 | 0.46 | 0.76 | – | 1.72 | 0.90 | 0.63 |
C. aguayoi | USNM 785110 | This work | ♀, juv | 1.72 | 2.47 | 1.25 | 1.25 | 0.60 | 0.50 | 0.44 | 3.12 | – | 1.11 | 0.22 | 0.56 | – | 1.38 | 0.65 | 0.49 |
C. aguayoi | USNM 782527 | This work | ♂, juv | 1.70 | 2.50 | 1.28 | 1.30 | 0.68 | 0.51 | 0.48 | 3.20 | 2.13 | 0.98 | 0.25 | 0.50 | – | 1.22 | 0.64 | 0.46 |
C. aguayoi | 013CAB | This work | ♀, juv | 1.56 | 2.20 | 0.95 | 0.90 | 0.56 | 0.39 | 0.38 | 2.40 | 1.80 | 0.78 | – | – | – | – | – | – |
C. aguayoi | 011CAB | This work | ♂, juv | 1.80 | 2.48 | 1.58 | 1.58 | 0.75 | 0.54 | 0.44 | 3.70 | 2.32 | – | – | – | – | – | – | – |
C. aguayoi | USNM 782825 | This work | ♂ | 1.56 | 2.06 | 1.00 | 1.00 | 0.56 | 0.44 | 0.34 | 2.63 | – | – | – | – | – | – | – | – |
C. aguayoi | USNM 392962 | This work | ♂ | 2.03 | 2.72 | 2.50 | 2.66 | 0.95 | 0.67 | 0.56 | 3.80 | 2.55 | 1.53 | 0.56 | – | – | 1.40 | 0.78 | 0.57 |
C. aguayoi | USNM 392988 | This work | ♂ | 2.00 | 2.69 | 1.88 | 1.88 | 0.75 | 0.56 | 0.48 | 3.56 | – | – | – | – | – | – | – | – |
C. aguayoi | USNM 392977 | This work | ♂ | 1.97 | 2.56 | 1.83 | 1.88 | 0.74 | 0.59 | 0.48 | 3.50 | 2.50 | 1.13 | 0.32 | 0.56 | – | 1.35 | 0.67 | 0.48 |
C. aguayoi | USNM 392775 | This work | ♀ | 2.56 | 2.63 | 1.47 | 1.40 | 0.79 | 0.52 | 0.48 | 3.16 | 2.38 | – | – | – | – | – | – | – |
C. bahoruco | Holotype | Teruel 2016 | ♂ | 2.23 | 2.70 | 1.10 | 1.57 | 0.70 | 0.50 | 0.50 | 4.00 | 2.80 | – | – | – | – | – | – | – |
C. bahoruco | Paratype | Teruel 2016 | ♀ | 2.75 | 3.40 | 1.72 | 2.15 | 0.90 | 0.70 | 0.67 | 5.22 | 3.50 | – | – | – | – | – | – | – |
C. belizensis | HUJ INV AMB 117, holotype | Miranda et al. 2016b | ♂ | 1.72 | 2.78 | 1.56 | 1.56 | 0.91 | 0.66 | 0.51 | 4.63 | 3.20 | 1.52 | 0.40 | 0.76 | – | 1.80 | 1.04 | 0.60 |
C. belizensis | HUJ INV AMB 118, paratype | Miranda et al. 2016b | Juv | 1.78 | 2.33 | 1.20 | 1.12 | 0.68 | 0.50 | 0.46 | 3.44 | 2.63 | 1.15 | 0.30 | 0.58 | – | 1.50 | 0.88 | 0.55 |
C. belizensis | HUJ INV AMB 118, paratype | Miranda et al. 2016b | ♀ | 1.97 | 2.84 | 3.20 | 2.19 | 1.81 | 0.94 | 0.53 | 4.35 | 3.20 | 1.56 | 0.41 | 0.72 | – | 1.97 | 1.06 | 0.51 |
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.
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Charinus bahoruco Teruel, 2016
Miranda, Gustavo Silva de, Giupponi, Alessandro P. L., Prendini, Lorenzo & Scharff, Nikolaj 2021 |
Charinus sp.
Armas L. F. 2006: 229 |
Armas L. F. 2004: 39 |
Armas L. F. & Perez A. 2001: 50 |