Malagiella ranavalona, Ubick & Griswold, 2011
publication ID |
https://doi.org/ 10.1206/356.1 |
persistent identifier |
https://treatment.plazi.org/id/03C2C67F-FFBF-FF9A-F0D8-FDFBFB84F965 |
treatment provided by |
Tatiana |
scientific name |
Malagiella ranavalona |
status |
sp. nov. |
Malagiella ranavalona View in CoL , new species Figures 329–344 View Figs View Figs , 487 View Fig , maps 1, 2, 4; table 1
TYPE: Female holotype from forêt autour du Palais de la Reine Ranavalona, env., Ambohimanga, 20 km N Antananarivo, 1400 m, Antananarivo Province, Madagascar (9 Dec 1989, B. Hauser), deposited in NHMB (Bern-Mad-89/59, PBI _OON 03637).
ETYMOLOGY: The species is named after the type locality.
DIAGNOSIS: This species differs from others in the group by the moderately sinuous receptaculum, W/L 5 0.76 (figs. 339–344).
MALE: Unknown.
FEMALE (PBI_OON 03637): Total length 1.61 (1.50–1.61), carapace length 0.60, width 0.49, N 5 2. CEPHALOTHORAX (figs. 329 –331, 333–335): Eyes small, subequal; eye area about 0.40 carapace width, subequal to clypeus length (figs. 331, 334). ABDOMEN (figs. 332, 336–338): Pedicel tube short (fig. 337), scutum dorsal extension short, about 0.3 pedicel diameters. Dorsal scutum weakly sclerotized, pale orange, covering about 0.5 abdomen length, 0.3 abdomen width (fig. 330). LEGS: Patella plus tibia I nearly as long as carapace. Leg spination (in addition to typical pattern): tibia IV v0-0-2. GENITALIA: Postepigastric scutum weakly sclerotized; receptaculum moderately sinuous, W/L 5 0.76 (figs. 341–344).
OTHER MATERIAL EXAMINED: MADA- GASCAR: Antananarivo Province: Ambohimanga, 20 km N Antananarivo, forêt autour du Palais de la Reine Ranavalona, env., 1400 m, 9 Dec 1989 (C. Lienhard, NHMB Bern-Mad-89/60, PBI_OON 03919), 1♀.
DISTRIBUTION: Known only from the type locality in central Madagascar.
NHMB |
Natural History Museum Bucharest |
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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