Priceiella (Camurnirmus) paulbrowni Gustafsson & Bush, 2017

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 : 182-185

publication ID

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

publication LSID

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

DOI

https://doi.org/10.5281/zenodo.5296985

persistent identifier

https://treatment.plazi.org/id/832187E9-FF3F-FF7B-FF74-61F8FE85FA63

treatment provided by

Plazi

scientific name

Priceiella (Camurnirmus) paulbrowni Gustafsson & Bush
status

sp. nov.

Priceiella (Camurnirmus) paulbrowni Gustafsson & Bush , new species

( Figs 292–299 View FIGURES 292 – 293 View FIGURES 294 – 299 )

Type host. Garrulax leucolophus diardi (Lesson, 1831) —white-crested laughinthrush. Type locality. Phu Khiao , Chaiyaphum Province, Thailand.

Other host. Garrulax leucolophus belangeri Lesson, 1831 — white-crested laughingthrush.

Diagnosis. The male genitalia of Priceiella (Camurnirmus) paulbrowni n. sp. ( Figs 296–298 View FIGURES 294 – 299 ) are intermediate between Pr. (Cm.) hwameicola n. sp. ( Figs 288–290 View FIGURES 287 – 291 ) and Pr. (Cm.) nipalensis , and Pr. (Cm.) rhinocichlae ( Eichler, 1957) . As in Pr. (Cm.) hwameicola ( Fig. 289 View FIGURES 287 – 291 ) and Pr. (Cm.) nipalensis , the distal mesosome is rounded triangular in Pr. (Cm.) paulbrowni ( Fig. 297 View FIGURES 294 – 299 ), but as in Pr. (Cm.) rhinocichlae the distal mesosome of Pr. (Cm.) paulbrowni ( Fig. 297 View FIGURES 294 – 299 ) is also dominated by a broad transversal thickening, and the parameres are almost as long as those of Pr. (Cm.) rhinocichlae . In Pr. (Cm.) hwameicola ( Fig. 289 View FIGURES 287 – 291 ) and Pr. (Cm.) nipalensis the distal thickening of the mesosomal lobes are more slender and not medianly continuous, and the parameres are much shorter. In both Pr. (Cm.) rhinocichlae and Pr. (Cm.) paulbrowni ( Fig. 296 View FIGURES 294 – 299 ) the distal half of the basal apodeme is much wider than the proximal half, whereas in Pr. (Cm.) nipalensis and Pr. (Cm.) hwameicola ( Fig. 288 View FIGURES 287 – 291 ) the basal apodeme is about equally wide in distal and proximal halves. In both Pr. (Cm.) rhinocichlae and Pr. (Cm.) paulbrowni ( Fig. 297 View FIGURES 294 – 299 ), the horn-shaped lateral extensions of the gonopore originate from the proximal margin of the gonopore, whereas in Pr. (Cm.) hwameicola ( Fig. 289 View FIGURES 287 – 291 ) these extensions originate from the lateral margins of the gonopore.

Priceiella (Camurnirmus) paulbrowni can be separated from Pr. (Cm.) rhinocichlae by the following characters: distal mesosome quadratic in Pr. (Cm.) rhinocichlae but rounded triangular in Pr. (Cm.) paulbrowni ( Fig. 297 View FIGURES 294 – 299 ); parameres with characteristic notch on lateral margin about 1/3 from distal tip associated with pst 2 in Pr. (Cm.) rhinocichlae , but parameres without such notch in Pr. (Cm.) paulbrowni ( Fig. 298 View FIGURES 294 – 299 ); gonopore longer than wide in Pr. (Cm.) rhinocichlae , but wider than long in Pr. (Cm.) paulbrowni ( Fig. 297 View FIGURES 294 – 299 ). Vulval chaetotaxy partially overlapping between Pr. (Cm.) rhinocichlae an Pr. (Cm.) hwameicola ( Fig. 299 View FIGURES 294 – 299 ), but Pr. (Cm.) rhinocichlae has 5– 7 vss [7–9 in Pr. (Cm.) hwameicola ]. Females of Pr. (Cm.) rhinocichlae lack the psps of tergopleurite VIII present in Pr. (Cm.) paulbrowni ( Fig. 293 View FIGURES 292 – 293 ) and Pr. (Cm.) hwameicola ( Fig. 286 View FIGURES 285 – 286 ), but have ps on segment III, which are absent in Pr. (Cm.) paulbrowni and Pr. (Cm.) hwameicola .

Description. Both sexes. Head shape, structure, and chaetotaxy as in genus description and Fig. 294 View FIGURES 294 – 299 . Dorsal preantennal suture absent. Only marginal carina, mandibles, head nodi, and gular plate with dark pigmentation. Thoracic and abdominal segments as in genus and subgenus descriptions and Figs 292–293 View FIGURES 292 – 293 . Lateral tergopleurites and pleural incrassations as in Fig. 316 View FIGURES 315 – 318 .

Male. Abdominal chaetotaxy as in Table 2 and Fig. 292 View FIGURES 292 – 293 . Antero-lateral ends of subgenital plate as in Fig. 292 View FIGURES 292 – 293 . Basal apodeme narrows anteriorly ( Fig. 296 View FIGURES 294 – 299 ), with modest lateral expansion. Proximal mesosome rectangular. Gonopore ( Fig. 297 View FIGURES 294 – 299 ) broader than long, narrowly open distally. Mesosomal lobes broad, fused distally; 2 ames sensilla on each side anterio-lateral to gonopore ( Fig. 297 View FIGURES 294 – 299 ). Parameral heads ( Fig. 298 View FIGURES 294 – 299 ) irregular. Parameral blades long, tapering, widely divergent distally; pst1–2 sensilla. Measurements ex Garrulax leucolophus diardi (n = 5): TL = 1.34–1.49; HL = 0.36–0.39; HW = 0.36–0.38; PRW = 0.21–0.24; PTW = 0.34–0.38; AW = 0.51–0.62. Ex G. l. belangeri (n = 6): TL = 1.36–1.44; HL = 0.36–0.37; HW = 0.36–0.38; PRW = 0.23–0.24; PTW = 0.35–0.36; AW = 0.51–0.57.

Female. Abdominal chaetotaxy as in Table 2 and Fig. 293 View FIGURES 292 – 293 . Subgenital plate roughly triangular ( Fig. 299 View FIGURES 294 – 299 ), reaching vulval margin where it flares into cross-piece. Vulval margin ( Fig. 299 View FIGURES 294 – 299 ) gently rounded, with 3–5 long, slender vms on each side, and 7–9 short, thorn-like vss on each side; 4–5 long, slender vos; distal 2 vos near, but not median to, vss. Measurements ex Garrulax leucolophus diardi (n = 4 except n = 3 for TL and HL): TL = 1.59–1.87; HL = 0.38–0.44; HW = 0.38–0.42; PRW = 0.22–0.26; PTW = 0.37–0.42; AW = 0.56–0.63. Ex G. l. belangeri (n = 4): TL = 1.66–1.92; HL = 0.38–0.42; HW = 0.40–0.43; PRW = 0.23–0.27; PTW = 0.36–0.41; AW = 0.56–0.66.

Etymology. The species epithet is in honour of Paul Brown, Senior Curator of Sternorrhyncha, lice, and thrips at the NHML. His monumental efforts in loaning large numbers of specimens made this revision possible.

Type material. Ex Garrulax leucolophus diardi [some as Garrulax leucolophus ]: Holotype ♂, Phu Khiao, Chaiyaphum Province, Thailand, 28 Dec. 1952, R.E. Elbel, RE-980, RT-B-17561 (NHML). Paratypes: 1♀, same data as holotype (NHML); 1♂, 1♀, Kilos Mountains, Phu Khiao, Chaiyaphum Province, Thailand, 29 Dec. 1952, R.E. Elbel, RE-982, RT-B-17563, 24733 on reverse (OSUS); 1♂, 1♀, Ban Tham, Chiang Mai Province, Thailand, 19 Oct. 1972, GMP-693, 24734 on reverse (OSUS); 1♂, 1♀, Chiang Saen Kao, Chiang Rai Province, Thailand, 22 Feb. 1953, R.E. Elbel & H.G. Deignan, RE-2312, RT-B-12816 (PIPeR); 1♂, 1♀, Phu Nam Lang, Na Phung, Dan Sai District, Loei Province, Thailand, 7 Jun. 1955, R.E. Elbel, RE-5571 (PIPeR); 1♂, 1♀, Ban Na Nong Thum, Non Han Subdistrict, Chum Phae District, Khon Kaen Province, Thailand, 30 Oct. 1953, R.E. Elbel & B. Lekagul, RE-3095, RT-B-22574 (PIPeR).

Additional material examined (non-types)

Ex Garrulax leucolophus diardi [some as G. leucolophus ]: 1♂, Phu Lom Lo, Kok Sathon Subdistrict, Dan Sai District, Loei Province, Thailand, 15 Feb. 1955, R.E. Elbel, RE-4645, RT-B-31200 (USNM).

Ex Garrulax leucolophus belangeri [some as Garrulax leucolophus ]: 1♂, 1♀, Hin Laem, Tha Khanun, Kanchanaburi Province, Thailand, 2 Nov. 1952, R.E. Elbel & H.G. Deignan, RE-1396, RT-B-15836 (PIPER); 1♂, 1♀, same locality and collector, 9 Nov. 1952, RE-1466, RT-B-15852 (PIPeR); 1♂, 1♀, same locality and collector, 16 Nov. 1952, RE-1515, RT-B-17049 (PIPeR); 1♂, 1♀, same locality and collector, 19 Nov. 1952, RE-1536, RT-B- 17062 (PIPeR); 1♂, 1♀, same locality and collector, 9 Nov. 1952, RE-1466, RT-B-15852 (OSUS); 1♂, 1♀, same data as previous (USNM).1♂, 1♀, same locality and collector, 3 Nov. 1952, RE-1397, RT-B-15834, 24748 on reverse (NHML);

Remarks. We found no significant morphological differences between the material we examined from the two host subspecies.

GBIF Dataset (for parent article) Darwin Core Archive (for parent article) View in SIBiLS Plain XML RDF