Selenobrachys Schmidt, 1999

Acuña, Darrell C., Dumbrique, Maria Mikaela U., Ranido, Maricel C., Ragasa, Lorenz Rhuel P., Noriega, Charles Nylxon C., Mayor, Anna Beatriz R., Florendo Jr, Gregorio Antonio, Fadri, Mary Jane A., von Wirth, Volker, Santiago-Bautista, Myla R. & Guevarra Jr, Leonardo A., 2025, Taxonomic revalidation of Selenobrachys Schmidt, 1999 and Chilocosmia Schmidt & von Wirth, 1992 based on morphological and molecular analyses (Araneae, Theraphosidae), with the description of a new species from Romblon Island, Philippines, ZooKeys 1233, pp. 139-193 : 139-193

publication ID

https://doi.org/10.3897/zookeys.1233.128056

publication LSID

lsid:zoobank.org:pub:E82A9CA6-EC67-4050-A3A9-2A40AFB528FE

DOI

https://doi.org/10.5281/zenodo.15115072

persistent identifier

https://treatment.plazi.org/id/410F2332-9685-5190-92E7-CBDAB2140A79

treatment provided by

ZooKeys by Pensoft

scientific name

Selenobrachys Schmidt, 1999
status

stat. rev.

Genus Selenobrachys Schmidt, 1999 stat. rev.

Type species.

Selenobrachys philippinus Schmidt, 1999 , comb. rest., by original designation and monotypy.

Included species.

(2 species) S. philippinus Schmidt, 1999 , comb. rest., S. ustromsupasius sp. nov.

Diagnosis.

Selenobrachys stat. rev. differs from all other selenocosmiine genera (including Chilocosmia stat. rev.), except sister genera Orphnaecus and Phlogiellus , in having a long prolateral superior keel (PS) (= retrolateral keel in West et al. 2012) from base to tip with a pronounced basal lobe (BL) on the embolus of males (Figs 10 A – F View Figure 10 , 14 A – E View Figure 14 ). Selenobrachys stat. rev. differs from Orphnaecus , and Phlogiellus (i) in having an ovoid proximally truncated and distally mildly tapering lyrate patch on the prolateral maxilla, with rows of strong paddle-shaped bacillae possessing thick and strong shafts (Figs 7 F, G View Figure 7 , 1 E, F View Figure 1 , 17 E, F View Figure 17 , 20 E View Figure 20 ) (reniform lyrate morphology for Orphnaecus ; see above and Fig. 20 G View Figure 20 ; rudimentary patch of needleform rods, if present, for Phlogiellus ; see Nunn et al. 2016) and where the largest ones in the lowest row have a more pointed tip in prolateral view (Fig. 20 E View Figure 20 ); (ii) in having greater number of cheliceral strikers (<150; excluding tertiary rows) (Figs 8 C View Figure 8 , 13 C, D View Figure 13 , 17 C, D View Figure 17 ); (iii) in having a long and cylindrical palpal tibia in males (Figs 9 A – D View Figure 9 , 15 B, C View Figure 15 ) (proximally swollen and distally tapering in Phlogiellus and Orphnaecus ; see Fig. 15 A View Figure 15 and Nunn et al. 2016); and (iv) in having a broad and short, not reduced ends, almost symmetrical, tombstone-shaped spermathecal lobe in females (Fig. 18 A, B View Figure 18 ). It further differs from Orphnaecus in lacking long and dense dorsal scopulate palpal brush in adult males (Figs 9 D View Figure 9 , 15 B, C View Figure 15 ) and in having short sword-like femoral setation on prolateral femur I (Fig. 21 E – H View Figure 21 ). It also differs from Phlogiellus in having a greater number of labial cuspules (~ 331–760) and a wider fovea than the ocular tubercle ( Nunn et al. 2016; Sivayyapram et al. 2020).

Distribution.

Philippine endemic: Negros Is. ( Schmidt 1999; West et al. 2012) and Romblon Is. (this study; Fig. 22 View Figure 22 ). Probably restricted to West Visayas PAIC and Romblon PAIC.

Etymology.

A combination of two generic names, Selenocosmia and Chilobrachys (Seleno- + - brachys) ( Schmidt 1999). Gender is masculine.

Kingdom

Animalia

Phylum

Arthropoda

Class

Arachnida

Order

Araneae

Family

Theraphosidae

SubFamily

Selenocosmiinae

Tribe

Yamiini