Anarchonirmus 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 : 78-79

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.5296893

persistent identifier

https://treatment.plazi.org/id/832187E9-FFC7-FF8D-FF74-61F8FDA2FADB

treatment provided by

Plazi

scientific name

Anarchonirmus Gustafsson & Bush
status

gen. nov.

Anarchonirmus Gustafsson & Bush , new genus

Type species. Anarchonirmus albovittatus new species

Diagnosis. Anarchonirmus n. gen. does not appear to be very close to any of the previously treated genera. The male genitalia are most similar to those of Brueelia s. str. ( Figs 45–47 View FIGURES 44 – 48 ). Like in Brueelia s. str. ( Fig. 48 View FIGURES 44 – 48 ), the female subgenital plate of Anarchonirmus ( Fig. 121 View FIGURES 116 – 121 ) flares into a cross-piece; however in Anarchonirmus the cross-piece is medianly displaced. as3 and pns are absent in both Brueelia s. str. ( Fig. 44 View FIGURES 44 – 48 ) and Anarchonirmus ( Fig. 116 View FIGURES 116 – 121 ). However, unlike in Brueelia s. str. ( Fig. 44 View FIGURES 44 – 48 ), the antennae are sexually dimorphic in Anarchonirmus ( Figs 116– 117 View FIGURES 116 – 121 ), and whereas in Brueelia s. str. ( Figs 42–43 View FIGURES 42 – 43 ) the tergopleurites in are rectangular and reach the lateral margins of the abdomen, the tergopleurites of Anarchonirmus ( Figs 114–115 View FIGURES 114 – 115 ) are much reduced and no not reach the lateral margins of the abdomen. Brueelia s. str. lacks aps and psps on more anterior segments ( Figs 42–43 View FIGURES 42 – 43 ), but these are present in Anarchonirmus ( Figs 114–115 View FIGURES 114 – 115 ; see also Tables 2–3).

The structure and chaetotaxy of the head of Anarchonirmus ( Fig. 116 View FIGURES 116 – 121 ) is similar to that of Sychraella n. gen. ( Fig. 108 View FIGURES 108 – 113 ) and Teinomordeus n. gen. ( Fig. 77 View FIGURES 77 – 82 ). In all three genera the antennae are sexually dimorphic; however, the dimorphism is more extreme in Anarchonirmus ( Figs 116–117 View FIGURES 116 – 121 ) than in either of the other two genera ( Figs 77– 78 View FIGURES 77 – 82 , 108–109 View FIGURES 108 – 113 ). In Sychraella ( Figs 106–107 View FIGURES 106 – 107 ) and in Anarchonirmus ( Figs 114–115 View FIGURES 114 – 115 ) the ads is sexually dimorphic, and in both these genera the sternal plates and subgenital plates of both sexes have deeply concave lateral margins ( Figs 106–107 View FIGURES 106 – 107 , 114–115 View FIGURES 114 – 115 ). However, while male Sychraella ( Fig. 106 View FIGURES 106 – 107 ) have no setae on tergopleurites II–III, male Anarchonirmus ( Fig. 114 View FIGURES 114 – 115 ) have both aps , psps, tps , and ss on these segments. Female Sychraella have no setae apart from ps on tergopleurites II–VII ( Fig. 107 View FIGURES 106 – 107 ), yet both psps and ss are present on these segments in Anarchonirmus ( Fig. 115 View FIGURES 114 – 115 ).

Description. Both sexes. Head indented-dome shaped ( Fig. 116 View FIGURES 116 – 121 ). Marginal carina uninterrupted; displaced dorsally and posteriorly at osculum. Clypeo-labral suture does not reach the anterior margin of the head. Ventral carinae fused to short but broad ventral anterior plate continuous with marginal carina. Broad median fingers of ventral carinae protrude into clypeo-labral suture. Dorsal preantennal suture absent. Head setae as in Fig. 116 View FIGURES 116 – 121 ; ads sexually dimorphic; as3 and pns absent; vsms2 on lateral margins of ventral anterior plate; s1–2 and pts not visible in the material examined; s3–4 mesosetae. Coni short and broad, obscured almost entirely by lateral protrusions of the head in male. Antennae sexually dimorphic; male scapes ( Fig. 116 View FIGURES 116 – 121 ) swollen, longer than female scapes ( Fig. 117 View FIGURES 116 – 121 ). Temporal carinae not visible; mts 3 only temporal macrosetae. Gular plate slender, pentagonal.

Prothorax ( Figs 114–115 View FIGURES 114 – 115 ) rectangular; ppss on postero-lateral corner. Proepimera slender; median ends blunt. Pterothorax pentagonal; lateral margins divergent; posterior margin convergent to median point; mms moderately separated medianly. Meso- and metasterna not fused; 1 seta on postero-lateral corner of each side of each plate. Metepisterna moderate; median ends blunt. Leg chaetotaxy as in Fig. 25 View FIGURES 25 , except fI-v4, fI-p2–4, fII-v2, fIII-v2 absent; cI-d1, cI-v3, tII-d1 not visible in the material examined; cIII-v2–3 of about equal length.

Abdomen ( Figs 114–115 View FIGURES 114 – 115 ) oval. Abdominal chaetotaxy as in Table 2. Tergopleurites hook-shaped, encircling spiracle openings; tergopleurites II–IX+X in male and tergopleurites II–VIII in female widely separated medianly; tergopleurite IX+X in female continuous with lateral section of tergopleurite XI. Sternal plates with concave lateral margins; only anterior and posterior margin pigmented in female. Antero-lateral corners of tergopleurites thickened, but plates do not reach lateral margins of abdomen. Abdominal setae generally thick. Male subgenital plate of irregular shape, reaching posterior margin of abdomen. Female subgenital plate roughly triangular; anterior margin pigmented; distally reaches vulval margin where it flares; postero-lateral margins thickened. Vulval margin ( Fig. 121 View FIGURES 116 – 121 ) with slender vms, thorn-like vss; vos follow lateral margins of subgenital plate.

Basal apodeme ( Fig. 118 View FIGURES 116 – 121 ) constricted at mid-length, anterior end pointed. Proximal mesosome trapezoidal. Gonopore ( Fig. 119 View FIGURES 116 – 121 ) slight, open distally, associated anteriorly with lateral extensions. Mesosomal lobes elongated, rugose; lateral and distal margins serrated; ames and pmes not visible. Parameral heads ( Fig. 120 View FIGURES 116 – 121 ) blunt. Parameral blades elongated, slender; distinct heel at about half length ( Fig. 82 View FIGURES 77 – 82 ); pst1 not visible; pst2 microseta, lateral near distal tip of paramere.

Host distribution. Presently known only from the host genus Pomatostomus . We have seen some specimens from P. superciliosus ashbyi Mathews, 1911 , but these are too poorly preserved to compare with the material from P. temporalis strepitans .

Geographical range. New Guinea.

Etymology. The name Anarchonirmus is ultimately derived from Greek “ an- ” for “without” and “archos ” for “leader”. “Anarchy” usually denotes a form of socialist society in which there are no hierarchies or leaders. However “ anarchos ” is here used in the derived meaning of “chaotic, unruly”, referring to the wild mixture of morphological characters that defies close association with any of the other genera in the Brueelia -complex. “ Nirmus ” is a common generic suffix in louse taxonomy, referring to Nitzsch’s (1818) genus of the same name. Gender: masculine.

Remarks. Anarchonirmus was not included in the phylogeny of Bush et al. (2016), and its position within the Brueelia -complex is uncertain.

Included species

* Anarchonirmus albovittatus new species

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