Galapa gabito Huber, 2024
publication ID |
https://doi.org/ 10.11646/zootaxa.5419.3.1 |
publication LSID |
lsid:zoobank.org:pub:39C67C6C-C84F-457E-86AD-03AC5C507979 |
DOI |
https://doi.org/10.5281/zenodo.10791779 |
persistent identifier |
https://treatment.plazi.org/id/F5342F12-1164-666A-7C86-F9DCA409D156 |
treatment provided by |
Plazi |
scientific name |
Galapa gabito Huber |
status |
sp. nov. |
Galapa gabito Huber sp. nov.
Figs 2E, F View FIG , 12–16 View FIG View FIG View FIG View FIG View FIG
Diagnosis. Males are distinguished from known congeners by simple (not bifid) retrolateral process on procursus directed towards dorsal ( Fig. 12C View FIG ); from G. spiniphila also by absence of ventral apophyses on genital bulb (compare Fig. 12A View FIG with Fig. 17A View FIG ), by shape of distal bulbal apophysis ( Fig. 12C View FIG ; smaller than in G. spiniphila ), and by prolateral distal apophysis on genital bulb (arrow in Fig. 12B View FIG ). Females are distinguished from known congeners by distinctive sclerite in ventral wall of uterus externus (arrow in Fig. 16D View FIG ; visible in cleared specimens, but also in posterior view of uncleared specimens with slightly spread open epigynal cleft); internal genitalia ( Fig. 16C–F View FIG ) with bilobed membranous structure covered by posterior epigynal plate (similar to G. murphyi ), without median membranous process (as opposed to G. spiniphila ).
Etymology. The species name honors the Colombian novelist Gabriel García Márquez (1927–2014), considered one of the most significant authors of the 20 th century and known affectionately as Gabo or Gabito in Latin America. The epithet is used as a noun in apposition.
Type material. COLOMBIA: Magdalena • ♂ holotype; Santa Marta ; 11.2126°N, 74.2307°W; 110 m a.s.l.; 16 Sep. 2022; B.A. Huber leg.; MUSENUV-Ar 2657 GoogleMaps • 6 ♂, 3 ♀, paratypes (one male and one female used for SEM); same collection data as for holotype; MUSENUV-Ar 2658 GoogleMaps • 1 ♂, 1 ♀, paratypes (plus two cleared female abdomens); same collection data as for holotype; ZFMK Ar 24219 GoogleMaps .
Other material examined. COLOMBIA: Magdalena • 1 ♂, 15 ♀, in pure ethanol (two cleared female abdomens transferred to ZFMK Ar 24219); same collection data as for holotype; ZFMK Col272 GoogleMaps .
Description.
Male (holotype)
MEASUREMENTS. Total body length 0.96, carapace width 0.38. Distance PME-PME 35 µm; diameter PME 30 µm; distance PME-ALE 15 µm; distance AME-AME 10 µm; diameter AME 20 µm. Leg 1: 1.68 (0.46 + 0.12 + 0.44 + 0.38+ 0.28), tibia 2: 0.34, tibia 3: 0.30, tibia 4: 0.48; tibia 1 L/d: 9; diameters of leg femora 0.075, of leg tibiae: 0.050.
COLOUR (in ethanol). Prosoma and legs pale ochre-yellow, carapace without pattern, legs without darker rings; abdomen ochre-grey with indistinct internal marks.
BODY. Habitus as in Fig. 2E View FIG . Ocular area not raised. Carapace without thoracic groove. Clypeus slightly more protruding than in female, with sclerotized rim. Sternum slightly wider than long (0.26/0.23), with pair of small anterior processes near coxae 1 ( Fig. 13D View FIG ; 20 View FIG µm long, 20 µm diameter at basis). Abdomen globular. Gonopore with four epiandrous spigots ( Fig. 13E View FIG ). Spinnerets apparently as in female (see below; dirty in scanned male).
CHELICERAE. In general, very similar to congeners (cf. Fig. 3 View FIG ), with curved process proximally on fang ( Fig. 13C View FIG ); with stridulatory files consisting of ~30 ridges, distances between ridges proximally 2.0 µm, distally 1.1 µm ( Fig. 13A View FIG ), proximal ridges with further fine subdivision.
PALPS. As in Figs 12 View FIG , 14A–D View FIG ; coxa unmodified; trochanter without process; femur proximally with prolateral stridulatory pick, distally slightly widened but without modification; femur-patella joints slightly shifted towards prolateral side; tibia oval, with two trichobothria; tibia-tarsus joints slightly shifted towards retrolateral side; palpal tarsal organ strongly raised ( Fig. 14E View FIG ), diameter 5.5 µm, diameter of opening 1.3 µm; procursus with pointed retrolateral-distal process distinctively directed towards dorsal and with dorsal process curved towards prolateral and lodged in pocket of genital bulb ( Fig. 14B View FIG ); genital bulb with small distal apophysis and similar prolateral distal apophysis; sperm duct opening apparently on prolateral-ventral side directly on bulb.
LEGS. Without spines and curved hairs. With round cuticular plates ( Fig. 15D View FIG ; diameter 4–5 µm) and rimmed pores ( Fig. 15E View FIG ; outer diameter 3 µm, diameter of opening 0.3 µm) apparently on all leg segments. Sexually dimorphic short vertical hairs present on tibiae 1 and 2 ( Fig. 15A, B View FIG ), barely visible in dissecting microscope, length ~15 µm, diameter at basis 1.0 µm. Chemoreceptive hairs similar in size (length ~10 µm, diameter at basis 1.3 µm) but with side branch (cf. Fig. 15F View FIG ). Retrolateral trichobothrium of tibia 1 at 57%; prolateral trichobothrium absent on tibia 1. Tarsus 1 with five pseudosegments, fairly distinct; leg tarsal organs capsulate. Main tarsal claws with ~9–11 tines.
Variation (male)
Tibia 1 in eight males (including holotype): 0.41–0.44 (mean 0.43).
Female
In general, similar to male ( Fig. 2F View FIG ) but sternum without pair of anterior humps, chelicerae without stridulatory files ( Fig. 13B View FIG ), cheliceral fangs unmodified, clypeus less protruding and without sclerotized rim, and palpal tarsal organ less raised ( Fig. 14F View FIG ) and slightly smaller (diameter 4.3 µm, diameter of opening 1.0 µm). Tibia 1 in 15 females: 0.37 – 0.40 (mean 0.39). ALS with one strongly widened spigot, one long pointed spigot, and apparently five cylindrical spigots, of which one is much wider than the others ( Fig. 13F View FIG ); PMS with two conical spigots; PLS without spigots. Epigynum ( Fig. 16A, B View FIG ) with simple semicircular anterior plate, weakly protruding, posteriorly not indented medially; posterior plate short and simple, with indistinct median division. Internal genitalia ( Fig 16C–F View FIG ) with distinctive sclerite in ventral wall of uterus externus (arrow in Fig. 16D View FIG ); apparently without pore plates; with bilobed membranous structure (without median process), covered by posterior epigynal plate.
Natural history. Most specimens were beaten out of dead cacti lying on the ground in a dry forest covering hills near the sea ( Fig. 5C View FIG ). They shared this microhabitat with another species of Ninetinae , an undescribed representative of Ibotyporanga .
Distribution. Known from type locality only, in Magdalena, Colombia ( Fig. 4 View FIG ).
ZFMK |
Zoologisches Forschungsmuseum Alexander Koenig |
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.