Guimaraesiella (Dicrurobates) nana Gustafsson, 2020

Gustafsson, Daniel R. & Bush, Sarah E., 2020, A new subgenus and eight new species of Guimaraesiella Eichler, 1949 (Phthiraptera: Ischnocera: Philopteridae: Brueelia-complex), Zootaxa 4885 (2), pp. 151-188 : 173-176

publication ID

https://doi.org/ 10.11646/zootaxa.4885.2.1

publication LSID

lsid:zoobank.org:pub:081203D8-39FF-41C3-A79A-BB63F47AB3B1

DOI

https://doi.org/10.5281/zenodo.4332144

persistent identifier

https://treatment.plazi.org/id/DB544115-6FA9-42F0-BF19-F6AC47C3F120

taxon LSID

lsid:zoobank.org:act:DB544115-6FA9-42F0-BF19-F6AC47C3F120

treatment provided by

Plazi

scientific name

Guimaraesiella (Dicrurobates) nana Gustafsson
status

new species

Guimaraesiella (Dicrurobates) nana Gustafsson & Bush, new species

( Figs 43–49 View FIGURES 43–44 View FIGURES 45–49 )

urn:lsid:zoobank.org:act:DB544115-6FA9-42F0-BF19-F6AC47C3F120

Type host. Dicrurus hottentottus samarensis Vaurie, 1947 —hair-crested drongo.

Type locality. Mount Lobi Range , Tambis Burauen, Leyte Island, Philippines .

Diagnosis. Guimaraesiella (Dicrurobates) nana is morphologically closest to Guimaraesiella (Di.) lurida and Guimaraesiella (Di.) regis n. sp. (see below). However, it can be separated from Guimaraesiella (Di.) lurida by the following characters: (1) dorsal preantennal suture reaching ads in Guimaraesiella (Di.) nana ( Fig. 45 View FIGURES 45–49 ), but not in Guimaraesiella (Di.) lurida ( Fig. 31 View FIGURES 31–35 ); (2) aps present in male tergopleurite V and female tergopleurite VIII in Guimaraesiella (Di.) lurida ( Figs 29–30 View FIGURES 29–30 ), but absent on these segments in Guimaraesiella (Di.) nana ( Figs 43–44 View FIGURES 43–44 ); (3) proximal mesosome with more or less straight anterior margin and anteriorly rounded ventral sclerite in Guimaraesiella (Di.) nana ( Fig. 47 View FIGURES 45–49 ), but wide, with markedly concave anterior margin and anteriorly flat ventral sclerite in Guimaraesiella (Di.) lurida ( Fig. 33 View FIGURES 31–35 ).

Also, Guimaraesiella (Dicrurobates) nana can be separated from Guimaraesiella (Di.) regis by the following characters: (1) dorsal preantennal suture reaches the lateral margins of head in Guimaraesiella (Di.) regis ( Fig. 52 View FIGURES 52–56 ), but not in Guimaraesiella (Di.) nana ( Fig. 45 View FIGURES 45–49 ); (2) ventral anterior plate broader than long in Guimaraesiella (Di.) nana ( Fig. 45 View FIGURES 45–49 ), but longer than broad in Guimaraesiella (Di.) regis ( Fig. 52 View FIGURES 52–56 ); (3) aps absent on male tergopleurite V in Guimaraesiella (Di.) nana ( Fig. 43 View FIGURES 43–44 ), but present on this tergopleurite in Guimaraesiella (Di.) regis ( Fig. 50 View FIGURES 50–51 ); (4) male abdominal segment IV with 2 ps on each side in Guimaraesiella (Di.) nana ( Fig. 43 View FIGURES 43–44 ), but with 1 ps on each side in Guimaraesiella (Di.) regis ( Fig. 50 View FIGURES 50–51 ); (5) mesosome similar but more slender in Guimaraesiella (Di.) nana ( Fig. 47 View FIGURES 45–49 ) than in Guimaraesiella (Di.) regis ( Fig. 54 View FIGURES 52–56 ). Females can be separated by the shape of the head ( Figs 44. 51 View FIGURES 43–44 View FIGURES 45–49 View FIGURES 50–51 ) and the subgenital plate ( Figs 49 View FIGURES 45–49 , 56 View FIGURES 52–56 ).

Description. Both sexes. Head shape and chaetotaxy as in Fig. 45 View FIGURES 45–49 . Lateral margins of preantennal head straight to slightly convex, frons broadly flattened; marginal carina broad, irregular; dorsal preantennal suture reaches dsms and ads, but not lateral margin of head; ventral preantennal plate large, broadly crescent-shaped; coni broad, long; temples rounded; gular plate broadly rhombic with anterior and lateral points ( Fig. 45 View FIGURES 45–49 ). Thoracic and abdominal segments as in Figs 43–44 View FIGURES 43–44 .

Male. Thoracic and abdominal chaetotaxy as in Fig. 43 View FIGURES 43–44 ; aps absent on tergopleurites IV–V, but present on tergopleurites VI–VII. Genitalia as in Figs 46–48 View FIGURES 45–49 : basal apodeme oval, not constricted at mid-length, and with rounded anterior end ( Fig. 46 View FIGURES 45–49 ). Proximal mesosome broad, narrowing distally, and with convex lateral margins; ventral sclerite broadly rounded, not reaching anterior margin of mesosome; mesosomal lobes roughly triangular, with prominent but only slightly rugose lateral nodi; 2 ames sensilla on each side near anterior margin of mesosomal lobes; 2 pmes sensilla on each side of gonopore, near rugose nodi; gonopore obovoid, with broad marginal thickening. Parameral heads rounded, subtriangular ( Fig. 48 View FIGURES 45–49 ). Parameral blades slender, tapering only distally ( Figs 46, 48 View FIGURES 45–49 ). Measurements: Ex Dicrurus hottentottus samarensis (n = 11, except TL, where n = 9): TL = 1.22–1.48; HL = 0.29–0.40 (0.37); HW = 0.31–0.36 (0.34); PRW = 0.20–0.23 (0.22); PTW = 0.29–0.32 (0.31); AW = 0.40–0.47 (0.43).

Female. Thoracic and abdominal chaetotaxy as in Fig. 44 View FIGURES 43–44 ; psps absent on tergopleurite VIII. Subgenital plate slightly trapezoidal in anterior section; lateral submarginal bulges slender, pointed; vulval margin gently rounded, with 3–4 slender vms on each side, the most median vms much shorter than other vms; 5–7 short, thorn-like vss on each side; 5–6 short, slender vos on each side; distal 1 vos anterior to vss, much longer than other vos ( Fig. 49 View FIGURES 45–49 ). Measurements: Ex Dicrurus hottentottus samarensis (n = 29, except TL, where n = 23, and AW, where n = 28): TL = 1.40–1.78 (1.58); HL = 0.38–0.43 (0.41); HW = 0.33–0.40 (0.36); PRW = 0.20–0.24 (0.22); PTW = 0.24–0.36 (0.30); AW = 0.41–0.57 (0.49).

Etymology. The species epithet derives from “ nanus ” Latin for “dwarf”, referring to the relatively small size of this species compared to other members of Guimaraesiella (Dicrurobates) .

Type material. Ex Dicrurus hottentottus samarensis [as D. hottentottus striatus ]: Holotype ♂, Mount Lobi Range, Tambis Burauen, Leyte Island, Philippines, 3 May 1964, D.S. Rabor, B-90 ( BPBM). Paratypes: 4♂, 18♀, same data as holotype ( BPBM) ; 2♂, 3♀, same data, B-90 ( BPBM) ; 1♂, 13♀, same data, B-77 ( BPBM) ; 3♂, 3♀, same data ( BPBM) .

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