Homa Distant, 1908
publication ID |
https://doi.org/ 10.5281/zenodo.203357 |
DOI |
https://doi.org/10.5281/zenodo.6190853 |
persistent identifier |
https://treatment.plazi.org/id/482A227B-B22A-FFEB-8CAE-FF248D27FE98 |
treatment provided by |
Plazi |
scientific name |
Homa Distant, 1908 |
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Homa Distant, 1908 View in CoL
Homa Distant, 1908: 400 View in CoL . Type species. Homa insignis Distant, 1908 View in CoL , synonymised with Homa haematoptilus ( Kirkaldy, 1906) View in CoL by Dworakowska, 1969: 487.
Redescription. Red empoascines. Head distinctly wider than maximum width of pronotum ( Fig. 1 View FIGURES 1 – 14 ). Vertex subquadrate, in dorsal view equal to or slightly shorter than width between eyes, anterior margin rounded, coronal suture not extended beyond midlength of vertex ( Fig. 1 View FIGURES 1 – 14 ), profile of transition of vertex to face rounded ( Fig. 2 View FIGURES 1 – 14 ). Face short and convex, lateral frontal suture present ( Figs 2, 3 View FIGURES 1 – 14 ). Eyes large ( Figs 1–3 View FIGURES 1 – 14 ). Forewing narrow, veins RP, MP’ and MP’+CuA’ separate at their bases, all arise from longitudinal m cell, 2nd apical cell with margins subparallel but slightly broadened at apex, r cell narrower than c cell, both narrower than m and cua cells ( Fig. 4 View FIGURES 1 – 14 ). Hindwing with area bordered by vannal veins small, vein CuA unbranched apically ( Fig. 5 View FIGURES 1 – 14 ).
Abdominal sternal apodemes weakly developed ( Fig. 14 View FIGURES 1 – 14 ). Male pygofer elongate, strongly narrowing caudad, terminally scattered with rigid microsetae on each side of pygofer lobe, dorsal margin produced with lobe or not, ventral appendage absent ( Figs 6, 8 View FIGURES 1 – 14 ); dorsal bridge quite long ( Fig. 7 View FIGURES 1 – 14 ). Subgenital plate far exceeding pygofer, broad at base, abruptly constricted in basal 1/3 at dorsal margin and from there with a cluster of tapered or terminally truncated macrosetae forming the basal group, lateral macrosetae not numerous and uniseriate, fine microsetae inconspicuous or absent ( Figs 6, 10 View FIGURES 1 – 14 ). Paramere long, caudal part strongly narrowing and curved, bearing teeth apically and few setae basad of serrations ( Figs 6, 13 View FIGURES 1 – 14 ). Connective fused with base of aedeagus ( Figs 11, 12 View FIGURES 1 – 14 ). Aedeagus without preatrium and dorsal apodeme, shaft tubular, long, in lateral view slightly tapering distally, ending in unpaired apical process or two asymmetrical processes ( Figs 11, 12 View FIGURES 1 – 14 ). Anal tube process simple, curved anteriad and narrowing apically ( Figs 6, 9 View FIGURES 1 – 14 ).
Remarks. Homa was established by Distant (1908) with H. insignis Distant (1908) as the type species from Sri Lanka. Kato (1929, 1933) described two more species ( H. elongata Kato 1929 , H. rubrodorsata Kato 1933 ) from China ( Taiwan) and Japan. McAtee (1934) downgraded Homa as a subgenus of Empoasca Walsh but it was later restored to a generic rank by Evans (1947). Mahmood (1967) redescribed the genus based on the type specimen deposited in the Natural History Museum, London. Metcalf (1968) reconsidered Homa as a subgenus of Empoasca , but this treatment has not been accepted by Dworakowska in her following works; Dworakowska (1969) transferred Eupteryx haematoptilus Kirkaldy (1906) to Homa and synonymized Homa insignis Distant (1908) with Homa haematoptilus ( Kirkaldy, 1906) . Later, she transferred Homa upoluana Osborn (1934) to Dayus Mahmood (1967) ( Dworakowska, 1971) and Homa elongata Kato (1929) to Asialebra Dworakowska (1971) ( Dworakowska, 1993) . Dworakowska (1984) subsequently described Homa katoi from Malaysia. To date, three Homa species have been reported worldwide, distributed throughout the Austro-Oriental Region.
Mahmood (1967) redescribed the genus and listed the following diagnostic features: “connective narrowly Vshaped, short; aedeagus without preatrium or dorsal apodeme, shaft tubular, produced caudad, slightly curving dorsad and ending in an unpaired sharp apical process which is recurved, also with a thin, short basal process on each side of shaft”. His redescription and reillustration of Homa insignis appears to show the connective is separate from the base of the aedeagus. Furthmore, Mahmood (1967) compared Homa with Empoasca and noted “It differs from Empoasca in its lack of anal hooks and processes…..”. From the illustration of Homa katoi Dworakowska (1984) (see Dworakowska 1984: Figs 54 View FIGURES 44 – 56 , 60 View FIGURES 57 – 70 ) and also the Homa specimens deposited in NWAFU ( Figs 11, 12 View FIGURES 1 – 14 ), the male genitalia have the connective fused with the aedeagus base, and a distinct anal tube process is present ( Figs 6, 9 View FIGURES 1 – 14 ). Contrary to Mahmood’s (1967) description, Dayus Mahmood also has a distinct anal tube. Dayus was revised by Qin & Zhang (2007).
Homa belongs to the Usharia Dwor. group and is related to Dayus , Baguoidea Mahmood and Goifa Dworakowska. All have the forewing with all apical veins arising from the m cell, the connective fused with the base of the aedeagus and the hindwing with CuA unbranched. Homa differs from the other genera in having veins RP and MP of the forewing have a short distance confluent, the sternal abdominal apodemes weakly developed with tips not widely divergent, the subgenital plate with an angulate basolateral projection with a cluster of macrosetae forming the basal group, and the aedeagal shaft ending in an unpaired apical process or two asymmetrical processes.
Dworakowska (1993) studied the holotype of Homa elongata Kato (1929) , transferring the species to Asialebra Dworakowska , and noting that “at the time of examination of the specimen it was under custody of M. Kato’s widow.” She did not mention the repository of Homa rubrodorsata Kato in this or her subsequent papers. Because Kato’s original description is insufficient and the type of Homa rubrodorsata (1 female) cannot be located, the latter is treated as a species inquirenda and is omitted from the key.
Included taxa: H. haematoptila ( Kirkaldy, 1906) , H. katoi Dworakowska (1984) , H. rubrodorsata Kato (1933) and H. sinensis Qin & Zhang , sp. n.
Distribution. China (Yunnan and Taiwan Provinces), Japan, Sri Lanka, Philippines, Malaysia, Australia.
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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Typhlocybinae |
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Empoascini |
Homa Distant, 1908
Qin, Dao-Zheng, Liu, Yang & Zhang, Ya-Lin 2011 |
Homa
Dworakowska 1969: 487 |
Distant 1908: 400 |