Guimaraesiella (Cicchinella) hampuslybecki Gustafsson, Clayton

Gustafsson, Daniel R., Clayton, Dale H. & Bush, Sarah E., 2019, Twelve new species of Guimaraesiella (Phthiraptera: Ischnocera: Philopteridae) from “ babblers ” (Passeriformes: Leiothrichidae, Pellorneidae, Timaliidae) with a description of a new subgenus and a key to its species, Zootaxa 4543 (4), pp. 451-497 : 479

publication ID

https://doi.org/ 10.11646/zootaxa.4543.4.1

publication LSID

lsid:zoobank.org:pub:4F591303-AF92-4BBB-8B68-EDD27AA229DE

DOI

https://doi.org/10.5281/zenodo.5936034

persistent identifier

https://treatment.plazi.org/id/FD5A824B-CA66-44D8-ACFB-2D37C7CB8680

taxon LSID

lsid:zoobank.org:act:FD5A824B-CA66-44D8-ACFB-2D37C7CB8680

treatment provided by

Plazi

scientific name

Guimaraesiella (Cicchinella) hampuslybecki Gustafsson, Clayton
status

new species

Guimaraesiella (Cicchinella) hampuslybecki Gustafsson, Clayton & Bush, new species

( Figs 67–74 View FIGURES 67–68 View FIGURES 69–74 )

Type host. Heterophasia auricularis (Swinhoe, 1864) —white-eared sibia ( Leiothrichidae ).

Type locality. Liukuei , Taiwan .

Diagnosis. Guimaraesiella (C.) hampuslybecki is most similar to G. (C.) hannesundinae , with which it shares the characters listed under the latter species, above. However these two species can be separated by the following characters: (1) female subgenital plate with central reticulation in G. (C.) hampuslybecki ( Fig. 74 View FIGURES 69–74 ) but not in G. (C.) hannesundinae ( Fig. 66 View FIGURES 61–66 ); (2) single thorn-like setae lateral to vos in G. (C.) hannesundinae ( Fig. 66 View FIGURES 61–66 ) but no such seta in G. (C.) hampuslybecki ( Fig. 74 View FIGURES 69–74 ); (3) ss of female tergopleurite VIII short in G. (C.) hampuslybecki ( Fig. 68 View FIGURES 67–68 ) but long in G. (C.) hannesundinae ( Fig. 60 View FIGURES 59–60 ); (4) mesosomal ventral sclerite long and slender in G. (C.) hampuslybecki ( Fig. 72 View FIGURES 69–74 ) but short and blunt in G. (C.) hannesundinae ( Fig. 64 View FIGURES 61–66 ); (5) marginal thickenings of mesosomal lobes broad and not displaced at concavity in G. (C.) hannesundinae ( Fig. 64 View FIGURES 61–66 ) but slender and displaced medianly at concavity in G. (C.) hampuslybecki ( Fig. 72 View FIGURES 69–74 ); (6) ames sensilla in G. (C.) hampuslybecki (Fig, 72) but microsetae in G. (C.) hannesundinae ( Fig. 64 View FIGURES 61–66 ); and (7) papillate area of parameral heads more extensive in G. (C.) hannesundinae ( Fig. 65 View FIGURES 61–66 ) than in G. (C.) hampuslybecki ( Fig. 73 View FIGURES 69–74 ).

Description. Both sexes. Head rounded pentagonal ( Fig. 69 View FIGURES 69–74 ). Lateral margins of preantennal head convex. Dorsal preantennal suture does not reach lateral margin of head, and does not completely separate dorsal anterior plate from main head plate. Attachments of mandibular adductor muscles prominent. Head chaetotaxy as in Fig. 69 View FIGURES 69–74 ; pns microsetae. Coni long, broad, reaching distal margin of scape in female. Antennae sexually dimorphic. Gular plate roughly triangular. Thoracic and abdominal segments as in Figs 67–68 View FIGURES 67–68 . Reentrant heads of pleurites broader and blunter in male than in female.

Male. Scape as in Fig. 69 View FIGURES 69–74 . Thoracic and abdominal chaetotaxy as in Fig. 67 View FIGURES 67–68 . Genitalia as in Figs 71–73 View FIGURES 69–74 . Basal apodeme broader distally than proximally ( Fig. 71 View FIGURES 69–74 ), with rounded to slightly flattened proximal margin. Proximal mesosome roughly rectangular ( Fig. 72 View FIGURES 69–74 ), with bulging lateral margins. Ventral sclerite slender, with median elongation that almost reaches proximal margin of mesosome. Mesosomal lobes with strongly sinuous lateral margins. Marginal thickenings of mesosomal lobes displaced medianly at concavity, and continuous with broad, rounded trapezoidal nodi on distal mesosome. Gonopore complicated, as in Fig. 72 View FIGURES 69–74 ; 2 View FIGURES 1–2 ames sensilla on each side near antero-lateral corners of mesosomal lobes; gpmes not visible in examined material; 2 lpmes microsetae on each side situated in lateral concavity. Parameral heads irregular ( Fig. 73 View FIGURES 69–74 ). Parameral blades broad, tapering only distally; pst1–2 close together. Measurements (n = 7, except for TL where n = 6): TL = 1.11–1.23; HL = 0.32–0.34; HW = 0.32–0.35; PRW = 0.20–0.22; PTW = 0.31–0.34; AW = 0.44–0.49.

Female. Scape as in Fig. 70 View FIGURES 69–74 . Thoracic and abdominal chaetotaxy as in Fig. 68 View FIGURES 67–68 . ss of tergopleurite VIII much shorter than ss of tergopleurites II–VII. Subgenital plate as in Fig. 74 View FIGURES 69–74 , with extensive central reticulation; crosspiece with broad connection to subgenital plate. Vulval margin gently rounded ( Fig. 74 View FIGURES 69–74 ), with 2–3 slender vms on each side, and 6–10 thorn-like vss on each side; 4–5 vos on each side; distal vos situated anterior to vss. Measurements (n = 4): TL = 1.50–1.68; HL = 0.35–0.38; HW = 0.37–0.41; PRW = 0.21–0.26; PTW = 0.33–0.38; AW = 0.52–0.56.

Etymology. The species epithet is in honor of Hampus Lybeck (previously at the University of Gothenburg, Sweden) who assisted DRG while collecting lice in Sweden in 2007–2008, and has remained a good friend and bird-watching companion to DRG ever since.

Type material. Ex Heterophasia auricularis : Holotype Ƌ, Liukuei, Taiwan, T.C. Maa, TMT- 1764–1765 (UMSP). Paratypes: 1♂, 1♀, same data as holotype ( UMSP) ; 2♂, 1♀, Puli Nantou Hsien, Taiwan, Jan. 1964, T.C. Maa, TMT-185–188 ( UMSP) ; 1♂, 1♀, same data (PIPeR) ; 1♂, 1♀, same data except TMT-419 ( UMSP) ; 1♂, same data as holotype (PIPeR) .

UMSP

University of Minnesota Insect Collection

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