Novispathodus praebrevissimus, Leu & Bucher & Vennemann & Bagherpour & Ji & Brosse & Goudemand, 2022
publication ID |
https://doi.org/10.1186/s13358-022-00259-x |
DOI |
https://doi.org/10.5281/zenodo.13128029 |
persistent identifier |
https://treatment.plazi.org/id/038B1D1D-644A-FF95-FCA1-ECDBD165FC07 |
treatment provided by |
Felipe (2024-06-17 19:39:26, last updated 2024-11-29 15:07:42) |
scientific name |
Novispathodus praebrevissimus |
status |
sp. nov. |
Novispathodus praebrevissimus n. sp.
Figs. 17V View Fig ; 18A–D, F, J–N, O View Fig ?, P?, Q, S, T; 19R
1984 Neospathodus sp. aff. triangularis Bender ; Hatleberg & Clark, pl. 3, fig. 16
2014 Icriospathodus? zaksi (Buryi) ; Maekawa & Igo in Shigeta et al., fig. 192, nr. 10–13 (only).
2015 Novispathodus brevissimus (Orchard) ; Chen et al., p. 111, fig. 7.8.
2019 Novispathodus pingdingshanensis (Zhao & Orchard) ; Chen et al., fig. 3 nr. 5, 9 (only) fig. 5, nr. 6 (only).
2019 Novispathodus pingdingshanensis (Zhao & Orchard) ; Liu et al., p. 13, pl. 3, fig. 7 (only).
Etymology: According to its presumed relationship as a predecessor of Nv. brevissimus .
Holotype: specimen illustrated in fig. 24R
Paratype: specimen illustrated in fig. 24Q
Type locality: Lilong cliff, Luolou formation, Guangxi Province, China.
Type level: Luolou Formation, within latest Smithian black shales. Present in UAZ 5 which corresponds to the peak of the positive δ 13 Ccarb excursion and the Xenoceltites / Glyptophiceras beds.
Number of specimens.> 40.
Diagnosis. Short robust segminate P 1 element. Large rounded-to-sub-rounded basal cavity. Posterior margin often slightly concave. Small, largely fused denticles. Groove from basal pit to anterior end.
Description. Te segminate P 1 element shows a very large rounded to sub-rounded basal cavity in the posterior half of the element. A very deep basal groove is present from the basal pit to the anterior end of the lower margin. Te carina is relatively high with numerous small, fused denticles. Te cusp is undistinguishable. Te posterior lateral margin (posteriormost edge between basal cavity and last denticle) is slightly to strongly curved. Sometimes, the height of the posteriormost denticles is gradually but rapidly decreasing. In lateral view, the denticles tend to be radiating or recurved.
Remarks. Tis species is thought to be intermediate between Nv. pingdingshanensis and Nv. brevissimus . Te P 1 element of this species is very similar to that of Nv. pingdingshanensis , but the basal cavity is much larger and rounded. In comparison to Nv. brevissimus , this species is usually smaller and has a relatively bigger and more rounded basal cavity. Furthermore, the carina is lower, with less numerous denticles. Te new species is distinguished from the similar Novispathodus shirokawai ( Maekawa et al., 2018) by reclined and less pointy denticles, a larger, rounded basal cavity and a less triangular shape in lateral view. Compared to Ic. zaksi , the P 1 element of this species is less robust and has a relatively higher carina. Ns. expansus (Zhao & Orchard) has a very similar morphology to Nv. praebrevissimus n. sp., but it has a distinct conspicuous thickening in the middle part of its unit. Some specimens of Nv. praebrevissimus n. sp.
( Fig. 18L, O and P View Fig ) show a bulbous thickening in the posterior part of the carina but never as pronounced as in Ns. expansus .
Occurrence. Spitsbergen, Botneheia Formation ( Hatleberg & Clark, 1984). South China, Nanpanjiang basin: Jiarong, southern Guizhou ( Chen et al., 2015). Luolou Formation, within latest Smithian black shales. Present in UAZ 5 which corresponds to the peak of the positive δ 13 Ccarb excursion and the Xenoceltites / Glyptophiceras beds, Guangxi, South China (this study). Oman (Leu et al., submitted).
Chen, Y., Jiang, H., Lai, X., Yan, C., Richoz, S., Liu, X., & Wang, L. (2015). Early Triassic conodonts of Jiarong, Nanpanjiang Basin, southern Guizhou Province, South China. Journal of Asian Earth Sciences, 105, 104 - 121. https: // doi. org / 10.1016 / j. jseaes. 2015.03. 014
Hatleberg, E. W., & Clark, D. L. (1984). Lower Triassic conodonts and biofacies interpretations: Nepal and Svalbard. Geologica Et Palaeontologica, 18 (12), 101 - 125.
Maekawa, T., Komatsu, T., & Koike, T. (2018). Early Triassic conodonts from the Tahogawa Member of the Taho Formation, Ehime Prefecture, Southwest Japan. Paleontological Research, 22 (s 1), 1 - 62. https: // doi. org / 10. 2517 / 2018 PR 001
Fig. 17 Novispathodinae from Qiakong,Laren, Shanggang,and Lilong. Magnification is × 80.The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise. A–C, J, T, AA Novispathodus ex gr. pingdingshanensis (Zhao & Orchard);A, QIA138,PIMUZ 39226; B QIA138, PIMUZ 39227; C LAR202, PIMUZ 39228; J QIA136, PIMUZ 39229;T LIL504, PIMUZ 39230; AA LIL508,PIMUZ 39231. D–F, M–P, R, S, U, X, AB, AD Novispathodus pingdingshanensis (Zhao & Orchard); D QIA135, PIMUZ 39259; E LIL508,PIMUZ 39260; F LIL506, PIMUZ 39261; M LIL506, PIMUZ 39262; N LIL506,PIMUZ 39263; O LIL507, PIMUZ 39264; P LIL506, PIMUZ 39265; R LIL508,PIMUZ 39266; S LAR204,PIMUZ 39267; U LIL507, PIMUZ 39268; X LIL508, PIMUZ 39269; AB LIL508, PIMUZ 39270; AD LIL508, PIMUZ 39271. G, I, Q Novispathodus cf.?gryphus n. sp.; G QIA136, PIMUZ 39204; I QIA136, PIMUZ 39205; Q QIA135, PIMUZ 39206. H, K, L Novispathodus gryphus n. sp.; H QIA135, PIMUZ 39243; K LIL506, PIMUZ 39244; L LIL506,PIMUZ 39245. V Novispathodus praebrevissimus n. sp.; LIL507, PIMUZ 39273. W, Y, Z, AE Novispathodus ex gr. abruptus (Orchard); W LIL505, PIMUZ 39208; Y SHA346,PIMUZ 39209; Z LIL506, PIMUZ 39210; AE SHA346, PIMUZ 39211. AC sp. indet.; LIL504, PIMUZ 39295. AF Novispathodus pingdingshanensis (P1 cluster) (Zhao & Orchard); QIA136, PIMUZ 39272
Fig. 18 Novispathodinae from Laren and Lilong. Magnification is ×80.The scale bar is 400 μm. All elements are considered to be P1 elements if not specifically identified otherwise.A, B, D, F, L–N, Q, S, T Novispathodus praebrevissimus n. sp.; A LIL506,PIMUZ 39274; B LAR207, PIMUZ 39275; D LIL508, PIMUZ 39276; F LIL507, PIMUZ 39277;L LIL507, PIMUZ 39278; M LIL509, PIMUZ 39279; N LIL507,PIMUZ 39280; Q LIL507, PIMUZ 39281; S LIL507, PIMUZ 39282; T LIL507, PIMUZ 39283. C, O, R Novispathodus?praebrevissimus n. sp.; C LAR204,PIMUZ 39284; O LIL507, PIMUZ 39285; R LIL507, PIMUZ 39286. E, I Novispathodus ex gr. pingdingshanensis (Zhao & Orchard); E LIL507,PIMUZ 39232, I LIL507, PIMUZ 39233. G Triassospathodus aff. symmetricus (Orchard);LIL507, PIMUZ 39309. H Novispathodus ex gr. abruptus (Orchard); LIL507, PIMUZ 39212. J, K Novispathodus praebrevissimus (juvenile) n. sp.; J LIL507, PIMUZ 39287; K LIL507,PIMUZ 39288. P Novispathodus robustispinus (Zhao & Orchard); LIL507,PIMUZ 39290
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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Order |
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SuperFamily |
Gondolelloidae |
Family |
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SubFamily |
Novispathodinae |
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