Smeringopina iboga, Huber, Bernhard A., 2013
publication ID |
https://doi.org/ 10.11646/zootaxa.3713.1.1 |
publication LSID |
lsid:zoobank.org:pub:C5F0BC11-92C0-4B30-9DB3-200882AC8950 |
DOI |
https://doi.org/10.5281/zenodo.6161989 |
persistent identifier |
https://treatment.plazi.org/id/B20287ED-FFF6-FF89-B990-C238FCCD3EB1 |
treatment provided by |
Plazi |
scientific name |
Smeringopina iboga |
status |
sp. nov. |
Smeringopina iboga View in CoL new species
Figs. 143–146 View FIGURES 143 – 152 , 169, 179 View FIGURES 163 – 183 , 253–258 View FIGURES 253 – 258
Type. ♂ holotype from Gabon, Ngounié, near Moulandoufouala (1°38.1’S, 10°42.5’E), 110 m a.s.l., forest along road, 27.viii.2011 (B.A. & S.R. Huber), in ZFMK (Ar 10205).
Other material examined. GABON: Ngounié: near Moulandoufouala, same data as holotype, 4♀ together with holotype; same data, 2♀ in pure ethanol, in ZFMK (Gab 188).
Etymology. The name is a noun in apposition, derived from the iboga tree ( Tabernanthe iboga ) native to western Central Africa, a hallucinogen whose bark of the root is chewed for pharmacological or ritualistic purposes.
Diagnosis. Distinguished from known congeners by distinctive shape of procursus (very wide in lateral view, Figs. 253–254 View FIGURES 253 – 258 ); females are difficult to distinguish from similar species with distinct anterior ridge of epigynum ( Figs. 169 View FIGURES 163 – 183 , 257 View FIGURES 253 – 258 ; cf. S. moudouma , S. ndjole ).
Male (holotype). Total body length 3.7, carapace width 1.3. Leg 1: 36.9 (8.6 + 0.5 + 8.9 + 17.0 + 1.9), tibia 2: 5.7, tibia 3: 4.1, tibia 4: 5.7; tibia 1 L/d: 84. Distance PME-PME 135 µm, diameter PME 125 µm, distance PME- ALE 55 µm, distance AME-AME 25 µm, diameter AME 125 µm. Carapace ochre-yellow with brown triangular mark posteriorly and brown lateral margins; ocular area with brown mark posteriorly; clypeus and sternum brown; legs light brown, femora with two dark rings, tibiae with four dark rings; abdomen ochre-gray with dark pattern dorsally, laterally, and ventrally, ventral dark bands with lateral constriction. Habitus as in Fig. 146 View FIGURES 143 – 152 , ocular area slightly elevated, secondary eyes with indistinct ‘pseudo-lenses’; clypeus with pointed and slightly hooked apophysis near rim; deep thoracic pit and pair of shallow furrows diverging behind pit. Chelicerae as in Fig. 255 View FIGURES 253 – 258 , with lateral apophyses in very distal position, pair of rows of small frontal apophyses, without modified hairs. Palps as in Figs. 143–145 View FIGURES 143 – 152 ; coxa with indistinct retrolateral apophysis; trochanter with large, heavily sclerotized ventral apophysis with obtuse tip; femur with large retrolateral apophysis directed toward ventrally, proximal prolateral ridge, and weakly sclerotized ventral projection distally; prolateral femur-patella joint strongly shifted toward ventrally; tarsus with some longer and slightly stronger hairs dorsally; procursus very wide in lateral view, with complex membranous prolatero-ventral structures, without hinge ( Figs. 253–254 View FIGURES 253 – 258 ); bulb with simple process ( Fig. 256 View FIGURES 253 – 258 ; sperm duct apparently opens at basis of this process). Legs without spines and curved hairs, with few vertical hairs; retrolateral trichobothrium on tibia 1 at 1.5%; prolateral trichobothrium present on all tibiae; pseudosegments barely visible.
Female. In general similar to male; clypeus unmodified. Tibia 1 in 4 females: 6.6, 6.7, 6.7, 7.4. Epigynum anterior plate with distinct anterior ridge ( Figs. 169 View FIGURES 163 – 183 , 257 View FIGURES 253 – 258 ); posterior plate laterally with overhanging folds; internal genitalia as in Figs. 179 View FIGURES 163 – 183 and 258 View FIGURES 253 – 258 .
Natural history. Litter-dwelling species.
Distribution. Known from type locality only ( Fig. 114 View FIGURE 114 ).
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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