Pseudognaptodon Fischer, 1965
publication ID |
https://doi.org/ 10.11646/zootaxa.4778.3.3 |
publication LSID |
lsid:zoobank.org:pub:6D747D40-ACB2-473D-B41C-2DA04B10F225 |
DOI |
https://doi.org/10.5281/zenodo.3848227 |
persistent identifier |
https://treatment.plazi.org/id/03911A3F-FF8B-2658-91A3-FB27FEFCFEEE |
treatment provided by |
Plazi |
scientific name |
Pseudognaptodon Fischer, 1965 |
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Pseudognaptodon Fischer, 1965 View in CoL View at ENA
( Figs 1–47 View FIGURE 1 View FIGURES 2–11 View FIGURES 12, 13 View FIGURES 14–23 View FIGURE 24 View FIGURES 25–35 View FIGURE 36 View FIGURES 37–47 )
Pseudognaptodon Fischer, 1964: 207 View in CoL (invalid), 1965: 182, 1967: 973, 1977: 983; Shenefelt, 1975: 1133; Marsh, 1979: 175; van Achterberg, 1983: 26; Whitfield & Wagner, 1991: 793; Belokobylskij, 1993a: 43–44; Wharton, 1997: 257–260, 2017: 240–242; Cirelli et al. 2002: 89; Williams, 2004: 153–154 (diagnosis); Low et al., 2012: 5899. Type species (by original designation): Pseudognaptodon curticauda Fischer, 1965 View in CoL .
Williams (2004) recognized two species groups (both without medio-posterior depression of mesoscutum); one group with distinctly impressed and curved episternal scrobe, antero-lateral grooves of third metasomal tergite distinct and setose part of ovipositor sheath 0.5–0.9 × as long as hind basitarsus ( P. omissus View in CoL group) and one without distinct scrobe (at most present as shallow depression), antero-lateral grooves of third metasomal tergite indistinct or absent and setose part of ovipositor sheath less than 0.5 × as long as hind basitarsus ( P. curticauda View in CoL group). Unfortunately, these characters were not mentioned in the descriptions by Cirelli et al. (2002), but judging from the figured metasoma, only P. murupe Braga & Penteado-Dias, 2002 View in CoL , belongs to the P. omissus View in CoL group and the rest to the P. curticauda View in CoL group. Another problem is the existence of two primary homonyms: Pseudognaptodon striatus Williams, 2004 View in CoL (not P. striatus Braga & Penteado-Dias, 2002 View in CoL ), and here renamed P. williamsi van Achterberg , nom. n. in honour of Daryl Williams for his excellent revision, and P. carinatus Williams, 2004 View in CoL (not P. carinatus Cirelli & Penteado-Dias, 2002 View in CoL ) is here renamed into P. carinatoides van Achterberg , nom. n.
The only known non-American species, Pseudognaptodon ruficeps Belokobylskij, 1992 , from Vietnam, is an aberrant species because of its metasomal sculpture: the first–third metasomal tergites (except apical half of third tergite) are largely longitudinally striate or rugulose, and the basal area of the second tergite is only 0.05 × as long as second and third tergites combined, features not encountered in any of the 28 New World species ( Cirelli et al. 2002; Williams 2004). The new species from NW China (Shaanxi) fills a gap in the distribution but is very different from P. ruficeps . It only shares the extensively sculptured three basal metasomal tergites, but the sculpture itself is different. The genus is new for the Palaearctic region and the Chinese fauna, and it is only the second known species in the Old World.
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Gnamptodontini |
Pseudognaptodon Fischer, 1965
Tian, Xiao-Xia, Achterberg, Cornelis Van, Wu, Jia-Xuan & Tan, Jiang-Li 2020 |
Pseudognaptodon
Low, C. & Scheffer, S. J. & Lewis, M. L. & Gates, M. W. 2012: 5899 |
Williams, D. J. 2004: 153 |
Cirelli, K. R. N. & Braga, S. M. P. & Penteado-Dias, A. M. 2002: 89 |
Wharton, R. A. 1997: 257 |
Belokobylskij, S. A. 1993: 43 |
Whitfield, J. B. & Wagner, D. L. 1991: 793 |
van Achterberg, C. 1983: 26 |
Marsh, P. M. 1979: 175 |
Shenefelt, R. D. 1975: 1133 |
Fischer, M. 1964: 207 |