Kéler, 1936a : 257 Ansari, 1956a: 155 Brueelia Ansari, 1956a: 152 Brueelia Ansari, 1956a: 154 Brueelia Morphological revision of the hyperdiverse Brueelia - complex (Insecta: Phthiraptera: Ischnocera: Philopteridae) with new taxa, checklists and generic key Bush, Sarah E. Zootaxa 2017 2017-08-31 4313 1 1 443 Gustafsson & Bush Bush 2017 [151,505,656,682] Insecta Philopteridae Resartor Animalia Phthiraptera 103 104 Arthropoda genus gen. nov.     Brueelia  Kéler, 1936a: 257( in partim).   Type species.  Brueelia impressifrons Ansari, 1956a: 152ex  Trochalopteron affine affineBlyth, 1843.   Diagnosis.  Resartor  n. gen.is most similar to  Ceratocista  n. gen.; for a detailed comparison between these two genera see  Ceratocista. Lack of posand pns, as well as general habitus similar to  Aratricerca  n. gen.( Figs 168– 174) and  Turdinirmoides  n. gen.( Figs 175–181), and members of these two genera also have thumb-like median extensions on the ventral carinae and slender proximal mesosomes. Leg chaetotaxy of  Ceratocista,  Resartor, and  Aratricerca, but not  Turdinirmoides, is identical, and  apsare absent in both sexes in all four genera. However, while in  Ceratocista( Fig. 154) and  Resartor( Fig. 162) the females lack ssentirely, these are found in tergopleurites II–VIII in both  Aratricerca( Fig. 169) and  Turdinirmoides( Fig. 176). In both  Aratricerca( Fig. 170) and  Turdinirmoides( Fig. 177) the dorsal preantennal suture reaches dsms, ads, and the lateral margin of the head near the dsms, where the marginal carina may be interrupted, and both genera have a ventral anterior plate. In  Resartor( Fig. 163), as in  Ceratocista( Fig. 155), the dorsal preantennal suture only interrupts the marginal carina submedianly, and does not reach either the dsmsnor the ads;  Resartorlacks a ventral anterior plate, but this is present in  Ceratocista. The female subgenital plate of  Resartorflares into a mediany interrupted cross-piece ( Fig. 167), just like in  Ceratocista( Fig. 160), but unlike  Aratricercawhich has a gently narrowed subgenital plate without a cross-piece ( Fig. 174); the vulval margin in  Turdinirmoides( Fig. 181) has a detached cross-piece. Parameral heads of  Resartorare bifid ( Fig. 166), as in  Aratricerca( Fig. 173) and  Ceratocista( Fig. 159), but unlike  Turdinirmoides( Fig. 180) in which they are folded into horseshoe-shapes. Parameral blades and mesosome of  Resartor( Figs 165–166) are also most similar to those of  Ceratocista( Figs 158–159), but  Resartorshares the somewhat angular mesosomal lobes and slender proximal mesosome with  Aratricercan. gen ( Fig. 172); the differences is structure of the male genitalia are considerable between the two genera, however.   Description. Both sexes. Head elongated pentagonal ( Fig. 163), frons often concave. Marginal carina interrupted only submarginally. Displaced section of marginal carina present at osculum, forming nail-like marginal carinal plate with sinuous posterior margin. Dorsal preantennal suture arising from interruptions of marginal carina not reaching adsor dsms; suture not medianly continuous posterior to dorsal anterior plate. Ventral carinae with finger-like median protrusion; carinae diffuse anterior to pulvinus. Ventral anterior plate absent. Head setae as in Fig. 163; avs2much shorter than avs3; pnsand posabsent. Coni small. Antennae monomorphic. Temporal carinae not visible;  mts3only macrosetae. Gular plate roughly triangular. Prothorax roughly rectangular ( Figs 161–162), but lateral margins convex; ppsson postero-latera corner. Proepimera hammer-shaped medianly. Pterothorax pentagonal; lateral margins divergent and posterior margin convergent to median point ( Figs 161–162). Meso- and metasterna not fused, 1 seta on postero-lateral corner on each side of each plate. mmswidely separated medianly. Leg chaetotaxy as in Fig. 25, except fI-p2, fI-v4absent. Abdomen ( Figs 161–162) oblong. Abdominal chaetotaxy differs among species ( Table 5). Terminal end of abdomen rounded in male, shallowly divided in female. Tergopleurites II–IX+X in male and tergopleurites II–VIII in females narrowly divided medianly, rectangular. Female tergopleurite IX+X fused with tergopleurite XI. Sternal plates square-shaped, not approaching pleurites. Pleural incrassations prominent. Re-entrant heads moderate to large. Malesubgenital plate trapezoidal. Female subgenital plate pentagonal ( Fig. 167), reaching vulval margin where it flares into medianly displaced cross-piece.   TABLE 5.Chaetotaxy of abdominal segments II–VIII of males of  Resartor. Trichoid setae of segment VIII are present in all species, and are not listed. Sets of setae differing from those of  Re. impressifronsare highlighted in bold. Material examined from all species is from their respective type hosts. Abbreviations:  aps= accessory post-spiracular seta; psps= principal post-spiracular seta; ps= paratergal seta; ss= sutural seta; sts= sternal seta;  tps= tergal posterior seta.     Species  ps   aps  psps   tps  ss  sts    Re. impressifrons IV–VIII – IV–VII VI–VIII II–VIII II–VI    Re. effronte  III–VIII  –  III–VII  IV–VIII II–VIII II–VI    Re. novofacies IV–VIII – IV–VII  IV–VIII II–VIII II–VI  Malegenitalia as in Fig. 164. Proximal mesosome slender, roughly trapezoidal, wideing slightly in proximal end. Gonopore ( Fig. 165) as convergent ventral thickenings, open distally and proximally or only distally and extended to reach lateral margins of mesosome. Mesosomal lobes small, angular, extending dorsally to slightly overlap with parameres. Parameral heads ( Fig. 166) bifid or folded into small heart-shapes. Parameral blades triangular; pst1–2not visible, but all examined males with partially everted male genitalia, and these could be overlooked.     Hostdistribution.All known species are found on members of Leiothrichidae.   Geographical range.Presently know only from SouthAsia.   Etymology.  Resartoris formed by Latin “ sartor”, meaning “ tailor”, with the prefix “ re-” meaning “back, again”; the full name thus means “The Re-tailor”, and is modified from the title of Thomas Carlyle's ( 1795–1881) “ Sartor Resartus”, first published in Fraser's Magazine between 1833–1834. The name is partially a homage to the idea, first suggested by Hamilton & Zuk (1982), that parasites could be the cause of colorful and extravagant plumages in birds; lice could thus be said to be “re-tailoring” the plumages of their hosts. However, there is also a likeness between the head structure the species of this genus and the structure of the needle plate of many modern sewing machines, reinforcing the “tailoring” impression of these lice. Gender: masculine.   Remarks.The phylogeny of Bush et al. (2016) included a single undescribed species of  Resartorfrom  Trochalopteron milnei(David, 1874), which was placed as sister to an undescribed  Aratricercafrom  Randia pseudozosteropsDelacour and Berlioz, 1931. These two in turn were placed close to  Indoceoplanetes  n. gen.and  Maculinirmus, but the placement received low support. However, no representative of several morphologically similar genera were included in that phylogeny, and the relationships among  Resartorand  Turdinirmusand  Turdinirmoides  n. gen.are unclear. Included species    *  Resartor effronte(  Ansari, 1956a: 155)  n. comb.[in  Brueelia]  *  Resartor impressifrons(  Ansari, 1956a: 152) n. comb.[in  Brueelia] *  Resartor novofacies(  Ansari, 1956a: 154)  n. comb.[in  Brueelia] 1587279680 [199,1091,865,890] Host 104 105 1 Host 1587279683 [199,880,901,926] South 104 105 1 South