Modisimus simoni Huber, 1997
publication ID |
https://doi.org/ 10.5852/ejt.2020.718.1101 |
publication LSID |
lsid:zoobank.org:pub:F9E9A91E-488C-4DB1-9361-E788E9AC5BC1 |
DOI |
https://doi.org/10.5281/zenodo.4343879 |
persistent identifier |
https://treatment.plazi.org/id/03E887AD-FF1B-7ACF-FDD5-FDE5FB20FCB9 |
treatment provided by |
Valdenar |
scientific name |
Modisimus simoni Huber, 1997 |
status |
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Modisimus simoni Huber, 1997 View in CoL
Figs 719–720 View Figs 717–724 , 725–729 View Figs 725–729 , 736–738 View Figs 736–741 , 1058
Modisimus simoni Huber, 1997b: 235 View in CoL , figs 5–7 (♂).
Hedypsillus [sic] minimus González-Sponga, 2009: 10 , figs 5a–i (1–9). New synonymy.
Misidentification
Hedypsilus simoni – González-Sponga 2010: 12 (see Modisimus culicinus View in CoL above).
Notes
The species was originally described from a single poorly preserved male from a poorly specified type locality (“Orinoco”) that Eugène Simon had erroneously identified as Hedypsilus (= Modisimus ) culicinus and that he had joined with the holotype of M. culicinus in a single vial. Part of the newly collected material below is from Ciudad Guayana, close to Ciudad Bolívar, which, given its historical importance, may well have been the collecting site of the type specimen in the late 19 th century. Collecting date and collector of the holotype are unknown (the material was not collected by E. Simon as erroneously stated in Huber 1997b).
The newly collected specimens were compared with the male holotype and with the types of Modisimus minimus . All relevant structures (male palp, male chelicerae, epigynum) were found to be identical.
Diagnosis
Males differ from similar tiny congeners [ M. culicinus (Simon, 1893) ; M. chiapa Gertsch, 1977 ; M. cienaga Huber & Fischer, 2010 ; M. david Huber, 1997 ] by dorsal process of procursus ( Figs 726– 728 View Figs 725–729 ); from M. culicinus also by absence of cuticular lobe frontally on ocular area (cf. Huber 1997a: fig. 1); from M. cienaga and M. david also by pair of apophyses frontally on chelicerae ( Huber 1997b: fig. 7; chelicerae unmodified in M. cienaga and M. david ). Male of M. tzotzile Brignoli, 1973 unknown. Females differ from M. david and M. tzotzile (and probably also from M. chiapa ) by presence of three pairs of marks on carapace ( Fig. 720 View Figs 717–724 ); from M. cienaga by shape of internal valve ( Fig. 729 View Figs 725–729 ; apparently very different in M. cienaga , but this might be an artifact, Huber et al. 2010: fig. 184); from M. culicinus by medially fused pore plates ( Figs 729 View Figs 725–729 , 738 View Figs 736–741 ; cf. Huber 1998a: fig. 7f).
Type material
M. simoni : ♂ holotype, MNHN (10529), Venezuela , “Orinoco”, E. Simon collection number 9629, date and collector unknown, examined.
M. minimus : ♂ holotype and 1 ♀ paratype, MIZA 105575 ( MAGS 1405), Venezuela , Portuguesa, “Acarigua (Pozo Blanco)” [approximately 9.533° N, 69.176° W], 7 Jul. 1995 (A. R. Delgado, M.A. González S.), examined.
New records
VENEZUELA – Bolívar • 6 ♂♂, 8 ♀♀, 1 juv., ZFMK (Ar 22058), and 7 ♀♀ in pure ethanol, ZFMK (Ven18-175), Ciudad Guayana , Parque La Llovizna (8.3111° N, 62.6755° W), 40 m a.s.l., 14 Nov. 2018 (B.A. Huber, O. Villarreal M.) GoogleMaps • 1 ♂, 1 ♀, ZFMK (Ar 22059), and 2 ♀♀ in pure ethanol, ZFMK (Ven18- 165), same locality at 8.3130° N, 62.6724° W, 50 m a.s.l., 11 Nov. 2018 (B.A. Huber, O. Villarreal M.). GoogleMaps – Mérida • 1 ♂, 4 ♀♀, ZFMK (Ar 22060), and 6 ♀♀ in pure ethanol, ZFMK (Ven20-114), near Las González (8.5066° N, 71.3183° W), 780 m a.s.l., leaf litter in dry forest near small stream, 9 Feb. 2020 (B.A. Huber, O. Villarreal M., Q. Arias C.). GoogleMaps – Trujillo • 2 ♂♂, 2 ♀♀, ZFMK (Ar 22061), and 3 ♀♀, 1 juv. in pure ethanol, ZFMK (Ven20-138), near El Encanto (9.7599° N, 70.7329° W), 250 m a.s.l., forest near stream, 13 Feb. 2020 (B.A. Huber, O. Villarreal M., Q. Arias C.) GoogleMaps .
Redescription
Male (Ciudad Guayana, ZFMK, Ar 22058)
MEASUREMENTS. Total body length 1.1, carapace width 0.53. Distance PME–PME 50 µm; diameter PME 60 µm; distance PME–ALE 60 µm; AME absent. Leg 1: 5.35 (1.55 +0.20 +1.40 +1.75 + 0.45), tibia 2: 1.10, tibia 3: 0.75, tibia 4: 1.25; tibia 1 L/d: 28; all femora approximately same width.
COLOR (in ethanol). Carapace pale ochre-grey, with three pairs of dark marks and dark V-mark on posterior border of ocular area; clypeus also darkened; sternum whitish; legs monochromous ochre-yellow; abdomen pale greenish-gray, with darker internal marks dorsally and white mark above spinnerets.
BODY. Habitus as in Fig. 719 View Figs 717–724 . Ocular area distinctly raised. Carapace with distinct thoracic groove. Clypeus unmodified. Sternum wider than long (0.36/0.26), unmodified. Abdomen globular.
CHELICERAE. With pair of small frontal apophyses ( Huber 1997b: fig. 7).
PALPS. As in Figs 725–726 View Figs 725–729 ; coxa with small retrolateral apophysis, trochanter barely modified, femur proximally with retrolateral process, distally with strong ventral apophysis; procursus ( Figs 727–728 View Figs 725–729 ) with distinctive dorsal spine, prolateral-distal pointed sclerite, and complex membranous elements; genital bulb with prominent curved apophysis and dorsal membranous protrusion.
LEGS. Without spines and curved hairs; with vertical hairs in high density on all femora; retrolateral trichobothrium of tibia 1 at 22%; prolateral trichobothrium absent on tibia 1; tarsus 1 with ~8 pseudosegments, fairly distinct.
Male (variation)
Tibia 1 in ten newly collected males: 1.20–1.40 (mean 1.31). Male holotype of M. minimus , total body length: 1.1 ( not 1.93 as in original description), tibia 1: 1.50, tibia 4: 1.35 ( not 1.72 as in original description). Several drawings of the M. minimus holotype in González-Sponga (2009) are wrong: the male ocular area is wider (PLE more lateral), the posterior border of the sternum is not concave (but straight), and the male chelicerae do not have two pairs of processes (but only one).
Female
In general similar to male ( Fig. 720 View Figs 717–724 ) but femora without (or very few) vertical hairs and legs with indistinct darker rings on femora (subdistally) and tibiae (proximally and subdistally). Tibia 1 in 15 newly collected females: 0.85–1.05 (mean 0.92). Epigynum ( Fig. 736 View Figs 736–741 ) simple trapezoidal plate, internal bluish ‘valve’ variably visible in uncleared specimens. Internal genitalia ( Figs 729 View Figs 725–729 , 737–738 View Figs 736–741 ) with medially fused pore plates and prominent frontal ‘valve’ with median receptacle. Female paratype of M. minimus , tibia 1: 1.05, metatarsus 1: 1.25 ( not 0.98 as in original description).
Distribution
Apparently widespread in Venezuela , recorded from the states Bolívar, Portuguesa, Trujillo, and Mérida (Fig. 1058). The map in Fig. 1058 gives Ciudad Bolívar as type locality, but this is speculative (see Notes above).
Natural history
At Ciudad Guayana, the newly collected specimens were mostly found in relatively dry leaf litter (a thick layer of palm leaves and dicot leaves) in a strongly altered area of the Park. Few specimens were collected from pieces of bark on the ground in a more natural forested area of the Park, together with Blancoa piacoa Huber, 2000 . Near Las González, the spiders were abundant in dry leaf litter in a forest fragment near a small stream at the base of an arid hill; the species did not seem to occur under rocks higher up the hill. Near El Encanto the spiders were collected under rocks in a forest; they ran rapidly as soon as the rock was moved. Some females had a large, whitish genital plug. Three egg sacs contained ~5– 8 eggs each.
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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Genus |
Modisimus simoni Huber, 1997
Huber, Bernhard A. & Villarreal, Osvaldo 2020 |
Hedypsilus simoni
Gonzalez-Sponga M. A. 2010: 12 |
Hedypsillus [sic] minimus González-Sponga, 2009: 10
Gonzalez-Sponga M. A. 2009: 10 |
Modisimus simoni
Huber B. A. 1997: 235 |