Brueelia inusta, Gustafsson & Grossi & Halajian & Engelbrecht, 2024
publication ID |
https://doi.org/ 10.11646/zootaxa.5446.1.5 |
publication LSID |
lsid:zoobank.org:pub:6D42C745-5B36-46CE-9958-3F83A33BEEC1 |
DOI |
https://doi.org/10.5281/zenodo.11106910 |
persistent identifier |
https://treatment.plazi.org/id/039CBE7B-4602-FFE1-2FC9-7BFDA985E175 |
treatment provided by |
Plazi |
scientific name |
Brueelia inusta |
status |
sp. nov. |
Brueelia inusta new species
( Figs 4 View FIGURES 1–10 , 14 View FIGURES 11–19 , 27–33 View FIGURES 27–28 View FIGURES 29–33 , 39–40 View FIGURES 37–40 )
Type host: Ploceus velatus tahatali Smith, 1836 —Southern masked weaver.
Type locality: Old Herbarium , University of Limpopo, Limpopo Province, South Africa.
Diagnosis. In the key of Gustafsson et al. (2019a), males of B. inusta n. sp. key out to Brueelia sima Gustafsson et al., 2019a , based on the abdominal chaetotaxy, and females key out to Brueelia semiscalaris . However, the morphologically most similar species to B. inusta is B. oschadlei n. sp.; for characters separating these two new species, see above.
Brueelia inusta can be separated from Brueelia sima by the following characters: lateral margins of preantennal head more convex in B. inusta ( Fig. 29 View FIGURES 29–33 ) than in B. sima ; proximal mesosome proportionately smaller and gonopore proportionately larger in B. inusta ( Fig. 31 View FIGURES 29–33 ) than in B. sima ; parameres much elongated in B. inusta ( Fig. 32 View FIGURES 29–33 ) compared to B. sima ; female vulval margin with only 1 vms on each side in B. sima , but with 4–6 vms on each side in B. inusta ( Fig. 33 View FIGURES 29–33 ).
Brueelia inusta can be separated from B. semiscalaris by the following characters: head proportionately rounder and broader in B. inusta ( Fig. 29 View FIGURES 29–33 ) than in B. semiscalaris ; female abdominal segments IV–VII with 2 ps on each side in B. semiscalaris , but with 1 ps on each side in B. inusta ( Fig. 28 View FIGURES 27–28 ); dark pigmentation of male subgenital plate more extensive in B. inusta ( Fig. 4 View FIGURES 1–10 ) than in B. semiscalaris ( Fig. 8 View FIGURES 1–10 ); male parameres slender and elongated, about 2 times as long as mesosome, in B. inusta ( Fig. 30 View FIGURES 29–33 ), but stouter, not elongated and less than 1.5 times as long as mesosome in B. semiscalaris ; proximal mesosome somewhat flattened and irregular in B. inusta ( Fig. 31 View FIGURES 29–33 ), but gently rounded in B. semiscalaris ; female vulval margin more flattened in B. semiscalaris than in B. inusta ( Fig. 33 View FIGURES 29–33 ), and with fewer vms (4–6) and vss (3–4) in B. inusta ( Fig. 33 View FIGURES 29–33 ) than in B. semiscalaris (6–7 and 7–8, respectively).
Description. Head rounded triangular ( Fig. 29 View FIGURES 29–33 ), lateral margins of preantennal area clearly convex, frons shallowly concave. Marginal carina slender, deeply displaced and somewhat widened at osculum. Ventral anterior plate small. Head chaetotaxy and pigmentation patterns as in Fig. 29 View FIGURES 29–33 . Preantennal nodi broad. Preocular nodi larger than postocular nodi. Marginal temporal carina variable in width, with undulating median margin. Thoracic and abdominal segments, chaetotaxy, and pigmentation patterns as in Figs 27–28 View FIGURES 27–28 .Anterior dark band of female subgenital plate continuous with central dark area. Male abdominal chaetotaxy: ss present on tergopleurites V–VIII; tps present on tergopleurites VII–VIII; psps present on tergopleurites VI–VII; aps present on tergopleurites VI–VII; ps present on segments IV–VIII. Female abdominal chaetotaxy: ss, tps, aps absent; psps present on tergopleurites VI–VII; ps present on segments IV–VIII. Proximal section of basal apodeme not clearly delimited and not illustrated; holotype ( Fig. 39 View FIGURES 37–40 ) with genitalia everted and folded anteriorly, and basal apodeme thus slightly constricted compared to other males ( Fig. 30 View FIGURES 29–33 ). Proximal mesosome trapezoidal, with irregular somewhat flattened, anterior margin ( Fig. 31 View FIGURES 29–33 ). Mesosomal lobes convergent distally, with extensive rugose areas. Gonopore large, rounded. Penile arms not extended beyond distal margin of mesosome. Parameres elongated, sinuous, with pst1–2 as in Fig. 32 View FIGURES 29–33 . Female subgenital plate rounded trapezoidal, with broad connection to cross-piece ( Fig. 33 View FIGURES 29–33 ). Vulval margin rounded convergent to median point, with 4–6 short, slender vms and 3–4 short, thorn-like vss on each side; 2–4 short, slender vos on each side of subgenital plate; distal 1 vos on each side median to vss. Measurements are given in Table 1 View TABLE 1 .
Etymology: The species epithet derives from “ inustus ”, Latin for “burnt”, referring to the pigmentation patterns.
Type material. Ex Ploceus velatus tahatali : Holotype ♂, Old Herbarium , University of Limpopo, Limpopo Province, South Africa, 11 Sep. 2014, coll. A. Halajian, SAFRING BC09995 ( NMHL) . Paratypes: 1♀, same data as holotype ( NHML) . 1♂, 1♀, same data as holotype, SAFRING BB72401 ( NHML) . 1♂, 1♀, same data as holotype, SAFRING BB72402 ( NHML) . 1♂, 1♀, Polokwane Game Reserve, Polokwane, Limpopo Province, South Africa, 11 Feb. 2012, coll. A. Halajian, Pve-PGR2 ( NHML) . 1♀, same data as previous, Pve-PGR3 ( NHML) . 1♂, 1♀, same data as previous, SAFRING CV27561 , Pve-PGR4 ( NHML) . 1♀, University of Limpopo , Limpopo Province, South Africa, 28 Sep. 2012, coll. A. Halajian, SAFRING CV27571 , Pve-PGR11 ( NHML) . 1♂, 1♀, same data as previous, SAFRING CV27573 , Pve-PGR12 ( NHML) . 1♀, De Loskop , Limpopo Province, South Africa, 7 Dec. 2012, coll. A. Halajian, SAFRING CV27598 , Pve-PGR17 ( NHML) . 1♂, 1♀, same data as previous, SAFRING CV65202 , Pve-PGR 20 ( NHML).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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