Brueelia phasmasoma Gustafsson & Bush

Bush, Sarah E., 2017, Morphological revision of the hyperdiverse Brueelia - complex (Insecta: Phthiraptera: Ischnocera: Philopteridae) with new taxa, checklists and generic key, Zootaxa 4313 (1), pp. 1-443: 48-51

publication ID

https://doi.org/10.11646/zootaxa.4313.1.1

publication LSID

lsid:zoobank.org:pub:A5Fdfba5-F992-44A8-84C2-1756C943C19B

persistent identifier

http://treatment.plazi.org/id/832187E9-FFA5-FFF1-FF74-63ADFAADFE9C

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Plazi

scientific name

Brueelia phasmasoma Gustafsson & Bush
status

new species

Brueelia phasmasoma Gustafsson & Bush  , new species

( Figs 56–62View FIGURES 56 – 57View FIGURES 58 – 62)

Type host. Coereba flaveola luteola (Cabanis, 1850)  —bananaquit.

Type locality. Cumuto, Sangre Grande, Trinidad, Trinidad and Tobago.

Diagnosis. Brueelia phasmasoma  n. sp. is immediately separated from all other species here placed in Brueelia  s. str. by the structure of the preantennal area, which is the same as that of Acronirmus ( Fig. 85View FIGURES 85 – 89). However, as2 and pos are absent in Acronirmus ( Fig. 58View FIGURES 58 – 62), but present in Br. phasmasoma  ( Fig. 58View FIGURES 58 – 62). In Acronirmus spp. ads is posterior to avs3, whereas in Br. phasmasoma  , as in all Brueelia  s. str., ads is anterior to avs3. In addition, the abdominal chaetotaxy of Acronirmus differ from that of Br. phasmasoma  (cf. Br. phasmasoma  in Table 3 with Acronirmus in Table 2, and Figs 56–57View FIGURES 56 – 57 with Figs 83–84View FIGURES 83 – 84).

Description. Both sexes. Head shape, structure, and chaetotaxy as in Fig. 58View FIGURES 58 – 62. Marginal carina interrupted laterally and medianly, premarginal carina absent. Dorsal preantennal suture arises from hyaline margin and lateral interruption of marginal carina, and is transversally continuous posterior to small, rounded pentagonal dorsal anterior plate. Ventral anterior plate small. Short vsms2 on lateral margins of clypeo-labral suture. Preantennal nodi small, blunt, do not reach mds. Coni slender, reaching to distal margin of scape. Pre- and post-ocular nodi small. Gular plate spade-shaped. Head largely translucent except dark pigmentation on post-marginal carina, preantennal nodi, margins of antennal socket, a dorsal band across antennal socket, flagellomeres II –III, pre- and post-ocular nodi, marginal temporal carina except at occiput, and anterior half of gular plate. Thoracic and abdominal segments as in genus description and Figs 56–57View FIGURES 56 – 57; 5 mms on each side, alternating between short and long setae. Proepimera broad, median ends curled around coxae II. Median ends of metepisterna broad, blunt. Body largely translucent, but dark pigmentation on lateral margins of pro- and pterothorax, proepimera, metepisterna, small nodi on all legs, and pleurites.

Male. Abdominal chaetotaxy as in Table 3 and Fig. 56View FIGURES 56 – 57; tps  on tergopleurites VII –VIII. Subgenital plate trapezoidal ( Fig. 56View FIGURES 56 – 57). Genitalia ( Fig. 59View FIGURES 58 – 62) typical for genus. Anterior end of basal apodeme cannot be seen in the material examined. Proximal mesosome narrowly rounded. Gonopore ( Fig. 60View FIGURES 58 – 62) widely open distally. Parameral blades ( Fig. 61View FIGURES 58 – 62) slightly elongated distally; pst1 sensillus, submarginal near distal tip; pst2 seta, lateral near distal tip. Measurements ex Coereba flaveola luteola  (n = 1): TL = 1.30; HL = 0.32, HW = 0.28; PRW = 0.17; PTW = 0.25; AW = 0.36.

Female. Abdominal chaetotaxy as in Table 3 and Fig. 57View FIGURES 56 – 57. Subgenital plate rounded triangular ( Fig. 62View FIGURES 58 – 62), flaring into cross-piece at vulval margin. Vulval margin ( Fig. 62View FIGURES 58 – 62) gently rounded, with 3–5 slender vms on each side, and 5–7 short, thorn-like vss on each side; 3–4 slender vos on each side anterior to cross-piece, and 1 slender vos on each side just anterior to vss. Measurements ex Coereba flaveola luteola  (n = 7): TL = 1.43–1.60; HL = 0.33–0.35; HW = 0.28–0.32; PRW = 0.17–0.19; PTW = 0.26–0.29; AW = 0.38–0.45.

Etymology. The species epithet is formed by Latin “ phasma ” for “ghost” and Greek “ soma ” for “body”, referring to the almost entirely translucent body of this species.

Type material. Ex Coereba flaveola luteola  : Holotype ♂, Cumuto, Sangre Grande, Trinidad, Trinidad and Tobago, 10 May 1960, TRVL-4363, Brit. Mus. 1974-636 ( NHML). Paratypes: 2♀, same data as holotype ( NHML); 2♀, Nariva Swamp, Sangre Grande / Rio Claro Mayaro, Trinidad, Trinidad and Tobago, 30 Sep. 1960, TRVL-4978, Brit. Mus. 1974-636 ( NHML); 3♀, Vega de Oropouche, Sangre Grande, Trinidad, Trinidad and Tobago, 24 Nov. 1959, TRVL-3675, Brit. Mus. 1974-636 ( NHML); 2♀, Vega de Oropouche, Sangre Grande, Trinidad, Trinidad and Tobago, 14 Apr. 1959, TRVL-2313, Brit. Mus.1974-636 ( NHML).

Remarks. Brueelia phasmasoma  was placed deep inside Brueelia  s. str. in the phylogeny of Bush et al. (2016). However, none of the species closely related to Br. phasmasoma  have similar modifications of the preantennal area. Specimens from Manacus manacus trinitatis (Hartert, 1912) and Volatinia jacarina (Linnaeus, 1766)  , both from Trinidad, have similar modifications of the preantennal area but, since only single females from each host were available to us, we cannot properly assess if these females belong to Br. phasmasoma  .

Williams (1982a) previously reported Brueelia  sp. from Coereba flaveola sanctothomae (Sundevall, 1870)  but, as she gave no details about its morphology, we cannot be certain if it is the same species as Br. phasmasoma  .

NHML

Natural History Museum, Tripoli