Tupigea angelim Huber, 2011
publication ID |
https://doi.org/10.1080/00222933.2010.524319 |
persistent identifier |
https://treatment.plazi.org/id/03A887D8-FF8B-FFAE-BB1B-D83DFE35FB03 |
treatment provided by |
Carolina (2021-04-06 18:35:39, last updated 2021-04-06 18:35:40) |
scientific name |
Tupigea angelim Huber |
status |
sp. nov. |
Tupigea angelim Huber sp. nov.
( Figures 4 A–C, 5A–E, 6A–H)
Tupigea sp. 1: Astrin et al. 2006: 445, 2007: 20.
Types
Male holotype and 2♂, 4♀ paratypes from Brazil, São Paulo, Ubatuba, Fazenda Angelim (23 ◦ 23.6 ′ S, 45 ◦ 03.8 ′ W), ∼ 50 m above sea level (a.s.l.), 16–18 December 2003 (B.A. Huber), holotype and 1♀ in IBSP , 2♂, 3♀ paratypes in ZFMK .
Etymology
The specific name is a noun in apposition, taken from the type locality.
Diagnosis
Easily distinguished from known congeners by armature on male chelicerae (pair of frontal apophyses, Figure 5C) and by dorsal worm-shaped projection of bulb ( Figures 5A, 6C); also by male palp (modifications of femur, procursus shape, embolic division of bulb, Figures 5A,B, 6C,D), and female genitalia ( Figures 5D,E, 6G).
Male (holotype)
Total body length 1.6, carapace width 0.67. Leg 1: 14.9 (3.7 + 0.2 + 3.8 + 5.9 + 1.3), tibia 2: 2.0, tibia 3: 1.4, tibia 4: 1.9, tibia 1 L / d: 72. Habitus as in Figure 4A; carapace ochre-yellow, darker around thoracic furrow, ocular area and clypeus light brown, clypeus medially with dark brown band that is lined by two cuticular ridges ( Figures 6A,B), sternum and legs ochre-yellow, legs with darker rings subdistally on femora and tibiae, abdomen greenish-grey with large darker marks on dorsal half. Distance PME–PME 70 µm, diameter PME 70 µm, distance PME–ALE 35 µm; AME absent, only irregular pigment spots. Ocular area slightly elevated, thoracic furrow shallow but distinct, clypeus unmodified ( Figure 6A). Chelicerae as in Figure 5C, with distinctive pair of frontal apophyses. Sternum wider than long (0.46 / 0.38), unmodified. Palps as in Figure 5A,B, coxa with indistinct retrolateral apophysis, trochanter barely modified, femur with proximal projection, tiny cones on prolatero-ventral side, tiny retrolateral apophysis, and small ventral apophysis distally, patella relatively long ventrally, procursus short, distally with distinctive sclerotized and membranous elements, bulb large, with distinctive dorsal worm-shaped projection and partly membranous embolic division with terminal apophysis and transparent flap. Palpal tarsal organ exposed ( Figure 6E). Legs without spines and curved hairs, with some vertical hairs on tibiae dorsally; retrolateral trichobothrium on tibia 1 at 22%; tarsus 1 with 16 pseudosegments, quite distinct. Anterior lateral spinnerets with two spigots each; gonopore without epiandrous spigots ( Figure 6F).
Variation. Tibia 1 in four other males: 3.7, 3.9 (type locality), 3.0, 3.3 (Rio das Pedras); in males from Rio das Pedras the tiny cones ventrally on the femur are replaced by a single slightly larger apophysis; otherwise palps and chelicerae identical.
Female
In general similar to male but without darker median band and cuticular ridges on clypeus; carapace medially and ocular area darker brown; tibia 1 in eight females: 1.6–2.0 (mean 1.85). Epigynum ( Figures 4B, 5D, 6G) frontal plate darkened medially, posterior margin sclerotized, posterior plate with pair of frontal indentations; internal genitalia as in Figure 5E. In females from Rio das Pedras the posterior margin of the frontal plate is barely sclerotized and less protruding, but the internal genitalia appear indistinguishable. Two females with genital plugs ( Figure 4C, 6H).
Distribution
Known from two localities in São Paulo and Rio the Janeiro states ( Figure 2).
Material examined
BRAZIL: São Paulo: Ubatuba, Fazenda Angelim : 3♂, 4♀ types above; same data, 5♀ in pure ethanol, in ZFMK. Rio de Janeiro: Reserva Ecológica Rio das Pedras (22 ◦ 59.5 ′ S, 44 ◦ 06.0 ′ W), 50 m a.s.l., night collecting, 25 September 2009 (B.A. Huber), 1♂, 3♀ in ZFMK; same locality but 22 ◦ 59.5 ′ S, 44 ◦ 06.0 ′ to 06.8 ′ W, 50–200 m a.s.l., day collecting, 26 September 2009 (B.A. Huber, A. Giupponi), 1♂, 3♀ in MNRJ (1♂, 2♀) and ZFMK (1♀) .
Astrin JJ, Huber BA, Misof B, Kluetsch CFC. 2006. Molecular taxonomy in pholcid spiders (Pholcidae, Araneae): evaluation of species identification methods using CO 1 and 16 S rRNA. Zool Scr. 35: 441 - 457.
Astrin JJ, Misof B, Huber BA. 2007. The pitfalls of exaggeration: molecular and morphological evidence suggests Kaliana is a synonym of Mesabolivar (Araneae: Pholcidae). Zootaxa 1646: 17 - 30.
Ribeiro MC, Metzger JP, Martensen AC, Ponzoni FJ, Hirota MM. 2009. The Brazilian Atlantic Forest: how much is left, and how is the remaining forest distributed? Implications for conservation. Biol Conserv. 142: 1141 - 1153.
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