Goniocotes rolandi, Gustafsson & Tian & Zou, 2021
publication ID |
https://doi.org/ 10.11646/zootaxa.4990.2.6 |
publication LSID |
lsid:zoobank.org:pub:641F7696-2DD6-4FF9-8758-9E5E3EFB201B |
DOI |
https://doi.org/10.5281/zenodo.5026569 |
persistent identifier |
https://treatment.plazi.org/id/039D8447-FFBE-7862-FF40-F9A4FD32FBA7 |
treatment provided by |
Plazi |
scientific name |
Goniocotes rolandi |
status |
sp. nov. |
Goniocotes rolandi new species
( Figs 10–11 View FIGURE 10 View FIGURE 11 , 13–15 View FIGURES 12–13 View FIGURES 14–15 )
Type host: Crossoptilon harmani Elwes, 1881 —Tibetan eared pheasant ( Phasianidae ).
Type locality: Southeast Tibet, China .
Diagnosis. Goniocotes rolandi new species is most similar to Goniocotes crossoptiloni Liu, 1990 . These two species can be separated by the following characters: male tergopleurites V–VI with 1 tps on each side and tergopleurite VII without tps in G. crossoptiloni , but tergopleurite V with 2–4 tps on each side, tergopleurite VI with 1–2 tps on each side, and tergopleurite VII with 1–2 tps on each side in G. rolandi ( Fig. 10 View FIGURE 10 ); male sternite IV–V with 2 sts on each side in G. crossoptiloni , but with 3–4 sts on each side in G. rolandi ( Fig. 10 View FIGURE 10 ); head of G. rolandi ( Figs 10–11 View FIGURE 10 View FIGURE 11 ) proportionately wider and with flatter frons, especially in female, than head of G. crossoptiloni ; vulval margins more or less gently rounded in G. crossoptiloni , but with pronounced median bulge in G. rolandi ( Fig. 13 View FIGURES 12–13 ); male genitalia not illustrated in sufficient detail for G. crossoptiloni , but appear to have shorter parameres and broader mesosome than those of G. rolandi ( Figs 14–15 View FIGURES 14–15 ).
Description. Both sexes. Head shape as in Fig. 10 View FIGURE 10 ; temples flaring with definite postero-lateral corner at aperture of mts1. Marginal carina of moderate width, widening anteriorly (more obvious in male). Head chaetotaxy as in Figs 10–11 View FIGURE 10 View FIGURE 11 ; os sexually dimorphic; s1–2 and s5–9 present, as well as one sensillum situated roughly on a line between pts and pns, which may be either of s3–4. Thoracic and abdominal segments as in Figs 10–11 View FIGURE 10 View FIGURE 11 . Reticulation covers almost all of tergal and subgenital plates, but is less distinct elsewhere. For clarity, we have here illustrated only parts of this reticulation in grey, to indicate the relative size of the cells in the pattern. Measurements as in Table 1 View TABLE 1 .
Male. Ocular seta macroseta ( Fig. 10 View FIGURE 10 ). Thoracic and abdominal chaetotaxy as in Fig. 10 View FIGURE 10 ; median section of pteronotum with one macroseta and one microseta on each side; tergopleurites II–IV with setal rows; tergopleurite V with 2–4 tps on each side; tergopleurite VI with 1–2 tps on each side (one specimen with no tps on one side); tergopleurite VII with one tps on each side. Basal apodeme long and slender ( Figs 14–15 View FIGURES 14–15 ). Mesosome present, roughly triangular dorsally ( Fig. 14 View FIGURES 14–15 ), but ventrally with distinct hook-shaped lateral extensions at about mid-length. One small sensillum on each side near the dorsal anterior margin; no other sensilla or setae visible. Postero-lateral corners of basal apodeme with rugose nodi; parameres slender and somewhat elongated.
Female. Ocular seta microseta ( Fig. 11 View FIGURE 11 ). Thoracic and abdominal segments and chaetotaxy as in Fig. 11 View FIGURE 11 . Vulval margin with distinct median bulge and lateral sections deeply concave ( Fig. 13 View FIGURES 12–13 ). Vulval chaetotaxy: 41–48 long, slender vms (often in double rows at least laterally) and 2–3 large, thorn-like vss on each side; oblique set with 5–8 vos of varying length on each side, typically with distal setae longer than more proximal setae.
Etymology: The specific epithet is in honour of the first author’s father, Roland Gustafsson, who spent many weekends taking him outdoors to watch birds, to camp, to enjoy nature, and introducing him to his first bird-ringing event outside Jönköping, Sweden, in the early 1990s. This laid the foundations of a solid interest in nature for the first author, who eventually devoted his life to biological research.
Type material. Ex Crossoptilon harmani : Holotype ♂, S.E. Tibet [ China], May 1912, R . Meinertzhagen, ID 3759, NHMUK010675935 About NHMUK [right-most male on slide, marked with black dot] ( NHMUK). Paratypes. 3♂, 6♀, same data as holotype, NHMUK010675934–5 About NHMUK ( NHMUK) .
R |
Departamento de Geologia, Universidad de Chile |
NHMUK |
Natural History Museum, London |
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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