Paraostenia voultensis Secrétan, 1985
publication ID |
https://doi.org/ 10.5852/ejt.2023.898.2295 |
publication LSID |
lsid:zoobank.org:pub:87EE2C76-1DDC-40DE-87E7-4D0E11A312DC |
DOI |
https://doi.org/10.5281/zenodo.8421994 |
persistent identifier |
https://treatment.plazi.org/id/C12F87D2-9954-FFFE-2D5E-F982FB12F7C4 |
treatment provided by |
Plazi |
scientific name |
Paraostenia voultensis Secrétan, 1985 |
status |
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Paraostenia voultensis Secrétan, 1985
Figs 5D View Fig , 16–20 View Fig View Fig View Fig View Fig View Fig
Paraostenia voultensis Secrétan, 1985: 388–389 , fig. 5c–h, l.
cf. Ostenia sp. – Secrétan & Riou 1983: 26–27, figs 1, 6–7.
Paraostenia voultensis – Rolfe 1985: fig. 4; 1992: fig. 1a. — Schram et al. 1999: 772, tab. 1. — Charbonnier 2009: 206, figs 233, 251, 339–340, tab. 14. — Charbonnier et al. 2010: 115, 121, fig. 5e, tabs 1–2; 2014: 375, tab. 1. — Schram 2014: 353, fig. 3d. — Ji et al. 2017: 174. — Ehiro et al. 2019: 330. — Rak et al. 2018: 268. — Braig et al. 2019: fig. 5.6, 5.31. — Van Roy et al. 2021: 1739. — Laville et al. 2021a: 310–311; 2021b: 92–94; 2021c: 305. — Schram & Koenemann 2022: fig. 41.4, tab. 41.2.
Original diagnosis ( Secrétan 1985)
As for genus.
Emended diagnosis
Paraostenia with a serrate dorsal margin and a dorso-lateral row of pores.
Material examined
Holotype FRANCE • La Boissine, La Voulte-sur-Rhône, Ardèche ; Callovian , Middle Jurassic ; morphotype 2; MNHN.F. R50977 .
Paratype FRANCE • 1 spec.; same collection data as for holotype; MNHN.F. R50979 .
Additional material
FRANCE • 73 specs; same collection data as for holotype; morphotype 2; MNHN.F. A29150 , A29231 , A29256 , A29300 A29320 to A29322 , A29326 , A29328 to A29338 , A29340 , A29341 , A29344 , A29346 , A29347 , A29351 , A29354 , A29355 , A29362 , A29369 , A29370 , A53132 , A53328 to A53330 , A53336 , A53340 , A84030 to A84038 A84041 , A84043 to A84058 , A84060 to A84063 , A84065 to A84071 , R50966 , R50978 • 4 specs; same collection data as for holotype; morphotype 2; MSNM i7597 , i18928 , i25037 , i25038 • 9 specs; same collection data as for holotype; morphotype 1; MNHN.F. A29339 , A29354 , A29357 , A29361 , A53131 , A84039 , A84040 , A84047 , A84055 , A84059 .
Measurements
See Table 2 View Table 2 .
Description
Shield morphology
Square-shaped to sub-trapezoidal shield in lateral view with an asymmetric anterior margin formed on a well-developed optic notch, a rounded or sharp antero-dorsal corner, a convex dorsal midline is slightly convex, with a large fin-like ( Fig. 18D–E View Fig ) or flat dorsal carina, a rounded postero-dorsal corner, a vertical or postero-ventrally tilted, concave posterior margin, a rounded postero-ventral corner and a ventral margin divided into a posterior half steeply descending antero-ventrally and a horizontal anterior one ( Figs 16 View Fig , 17A–D View Fig ). Rim of all free margin delimiting a marginal fold ( Fig. 16B, D View Fig ).
Shield macro-ornamentation
Presence of one straight and large medio-lateral carina, running along almost the entire length of the shield and divided into two parts by a longitudinal narrow furrow ( Figs 16A, C View Fig , 21A–B View Fig ). Presence of seven small serrations dorsally oriented on the anterior side of the dorsal carina and of seven serrations dorsally oriented, longer than the anterior ones on the posterior side ( Fig. 18D–E View Fig ).
At least 13 pores forming a sinuous row in the dorsal area of the shield, above the medio-lateral-carina ( Figs 16A, C View Fig , 18D–F View Fig ). Horseshoe-like ornamentation or field of punctuations covering the ventral area of the shield ( Fig. 19A, C, J View Fig ). Fields of punctuations also covering the surface of the dorsal area ( Fig. 19E–G View Fig ). Punctuations in the ventral area most probably correspond to degraded horseshoe-like ornamentation.
Presence of a hump either on the medio-ventral area of the shield or near the antero-ventral corner ( Figs 16A, C View Fig , 19H–J View Fig ).
Sensory structures
Rounded, stalked, compound eyes protruding from the optic notch and occupying most of it ( Figs 16 View Fig , 18B–C View Fig ). Eyes formed of hexagonal ommatidia (w = ~80 µm; l = ~80 µm; about 236 per mm²; Fig. 17F View Fig ).
Cephalic appendages
Antenniform structure only perceptible by the muscle fibres protruding from the optic notch and decreasing in diameter distally ( Fig. 17E View Fig ).
Raptorial appendages
Presence of three pairs of slender raptorial appendages recognised by the preservation of the muscles,
protruding from the ventral margin, posterior to the presumed cephalic appendages. Raptorial appendages consisting of two parts: a proximal postero-ventrally oriented and a distal one, antero-ventrally oriented. Articulation between both parts forming an elbow.
First pair of raptorial appendages ( Figs 16 View Fig , 19A, C View Fig ), the shortest, consisting of a proximal part with two podomeres: podomere 1 being 3.7 times as long as wide; podomere 2 being 4.7 times as long as wide and being longer than podomere 1. Distal part of the appendages formed by three podomeres: podomeres 3 being 4.4 times as long as wide; podomere 4 being 4.8 times as long as wide; podomere 5, the most distal one, being 3.1 times as long as wide.
Second pair of raptorial appendages consisting of a proximal part with two rectangular podomeres ( Fig. 18M, O View Fig ): podomere 1 not being well preserved; podomere 2 being 6.1 times as long as wide. Distal part of the appendage consisting of three podomeres: podomere 3 being 5.6 times as long as wide and bearing one spine on its medial side; podomere 4 being 5.2 times as long as wide and bearing three spines on its medial side; podomere 5 being 2.8 times as long as wide and ending distally in a cluster of three long spines.
Third pair of raptorial appendages, the longest, consisting of a proximal part formed by two podomeres, podomere 2 being 5.9 times as long as wide ( Fig. 18I–K View Fig ). Distal part consisting of three podomere: podomere 3 being 4.4 times as long as wide, bearing two spines on the distal part of its medial side; podomere 4 being 6.4 times as long as wide and bearing nine spines on its medial side, with the first four arranged in pairs; podomere 5 being 4.3 times as long as wide and ending distally with a cluster of three long spines.
Oval structure
Oval structure protruding from the ventral margin, behind the last pair of raptorial appendages ( Fig. 18G– H View Fig ). Structure associated with a lamellar structure in one specimen ( Fig. 17G View Fig ).
Posterior trunk
Nine rectangular pleural parts of trunk segments protruding from the posterior part of the ventral margin ( Figs 16B, D, G View Fig , 20 View Fig ). In some specimens, pleural part increasing in size until tp 6, then decreasing until tp 9 ( Fig. 16B, D, G View Fig ). In other specimens, pleural parts decreasing in size posteriorly with last one (tp 9) thinner than the rest ( Fig. 17H View Fig ). Proximally, they have a postero-dorsal orientation while they are curved downward distally. Trunk ending in a square segment, i.e., the telson, bearing a rounded structure ( Fig. 17I–J View Fig ). Field of setae visible on the telson.
Posterior trunk appendages
Nine pairs of appendages attached to the pleural part of the posterior trunk ( Fig. 20F–H View Fig ). Appendages oriented postero-dorsally and proximally consisting of a curved square-shaped plate ( Fig. 20H View Fig ) and ending distally in a styliform part ( Fig. 20I–J View Fig ). Last pair of appendages with a rounded distal plate.
Gills
Eight arcuate, lamellar gills preserved below the medio-lateral carina ( Fig. 19A–B View Fig ).
Remarks
Paraostenia voultensis displays an important variability for some features. For instance, some specimens have a trapezoidal shield with a vertical posterior margin and a horseshoe-like ornamentation ( Figs 17– 20 View Fig View Fig View Fig View Fig ), while others have a square-shaped shield with a postero-ventrally tilted posterior margin and no ornamentation ( Fig. 16 View Fig ). Moreover, it seems there is a slight difference in total length ( Fig. 21A View Fig ): the histogram shows a bimodal distribution that might indicate the presence of two different morphotypes.
Morphometry
In order to characterise the variability of Paraostenia voultensis and to confirm the presence of two morphotypes, we ran various morphometric and statistical analyses. In this section, we consider separately both P. voultensis putative morphotypes in order to test for their differences. Morphotype 1 corresponds to the small specimens with a square-shaped shield, a postero-ventrally tilted posterior margin, and no ornamentation. Morphotype 2 corresponds to bigger specimens having a square-shaped shield with a postero-ventrally tilted posterior margin and no ornamentation.
Descriptive statistics
The measurements made on Paraostenia voultensis allow us to test the homogeneity of the sample. With the exception of the length of the shield (Ls), histograms appear normally distributed for all measurements ( Fig. 21A View Fig ). According to the results of the Shapiro-Wilk test (W> 0.95; p> 0.13), all measurements probably follow a normal law.
Simple allometry
For Paraostenia voultensis ( Fig. 21 View Fig ; Table 3 View Table 3 ), a strong and significant correlation has been found for morphotype 2 (R² = 0.892, p-value <0.05) while it is non-significant for morphotype 1 (R² = 0.605, p-value = 0.222). The slope (likelihood ratio statistic equal to 0.4298, p-value = 0.5121) and the elevation (Wald statistic equal to 0.7178, p-value = 0.39687) are equal between the allometric line of both morphotypes. This indicates that there is no difference in static allometry of both morphotypes and that they are located on a similar allometric line.
For all other species, a strong and significant positive correlation has been found between shield length and shield height (R²> 0.86, p-value <0.02; Table 3 View Table 3 ).
Complex allometry
The first two principal components account for 89.0% of the variance ( Fig. 22A View Fig ). PC1 accounts mostly for variation in height and angle measurements while PC2 accounts mostly for variation in shield length (Supp. file 3). Size measurements appear to be correlated between them ( Fig. 22B View Fig ), but not with angles measurements, which also appear correlated between them.
Clustering analysis ( Paraostenia voultensis )
Based on the VAT, the dataset presents a good clustering tendency that is not confirmed by the Hopkins statistic (0.57), which indicates a low clustering tendency. An optimal number of three clusters for the K-Means analysis was determined. Results of the prediction are presented in Figure 22 View Fig . Cluster 1 corresponds to specimens identified as morphotype 1 while specimens identified as morphotype 2 are split between clusters 2 and 3.
Kilianicaris lerichei | Ostenocaris ribeti | Paraclausocaris harpa gen. et sp. nov. | Paraostenia voultensis General morphotype 1 morphotype 2 | |||
---|---|---|---|---|---|---|
elevation | 0.027 | -0.267 | -0.096 | -0.115 | -0.117 | -0.0574 |
slope | 0.827 | 0.986 | 0.9 | 0.943 | 0.88 | 0.88 |
R 2 | 0.93 | 0.973 | 0.894 | 0.923 | 0.605 | 0.892 |
p-Value | 2.75e- 05 | 0.0134 | 0.0547 | 4.21e- 17 0.222 | 4.06e- 13 |
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.
Kingdom |
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Phylum |
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Family |
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Genus |
Paraostenia voultensis Secrétan, 1985
Laville, Thomas, Forel, Marie-Béatrice & Charbonnier, Sylvain 2023 |
Paraostenia voultensis
Van Roy P. & Rak S. & Budil P. & Fatka O. 2021: 1739 |
Laville T. & Haug C. & Haug J. T. & Forel M. - B. & Charbonnier S. 2021: 310 |
Laville T. & Haug J. T. & Haug C. 2021: 92 |
Laville T. & Smith C. P. A. & Forel M. - B. & Brayard A. & Charbonnier S. 2021: 305 |
Ehiro M. & Sasaki O. & Kano H. & Nagase T. 2019: 330 |
Rak S. & Broda K. & Kumpan T. 2018: 268 |
Ji C. & Tintori A. & Jiang D. & Motani R. 2017: 174 |
Schram F. R. 2014: 353 |
Charbonnier S. & Vannier J. & Hantzpergue P. & Gaillard C. 2010: 115 |
Charbonnier S. 2009: 206 |
Schram F. R. & Hof C. H. J. & Steeman F. A. 1999: 772 |
Paraostenia voultensis Secrétan, 1985: 388–389
Secretan S. 1985: 389 |
Ostenia sp.
Secrétan & Riou 1983: 26-27 |