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Published October 5, 2020 | Version v1
Taxonomic treatment Open

Protocalymene Ross 1967

  • 1. Department of Earth and Environmental Sciences, 115 Trowbridge Hall, University of Iowa, Iowa City, Iowa 52242, USA. jonathan-adrain @ uiowa. edu; https: // orcid. org / 0000 - 0002 - 7000 - 1311
  • 2. University of Colorado Museum of Natural History, 265 UCB, University of Colorado, Boulder, Colorado 80309, USA. talia. karim @ colorado. edu; https: // orcid. org / 0000 - 0001 - 6514 - 963 X
  • 3. Department of Geosciences, Texas Tech University, P. O. Box 41053, Lubbock, Texas 79409 - 1053, USA.

Description

Protocalymene Ross, 1967

Type species. Protocalymene mcallisteri Ross, 1967, from the Antelope Valley Formation (Dapingian) of California, USA.

Other species. Protocalymene sp. of Ross (1970, p. 92, pl. 18, figs 2–5), Antelope Valley Formation, Ike’s Canyon, Monitor Range, Nye County, Nevada; Protocalymene sp. of Loch and Ethington (2017, p. 310, fig. 13.6), uppermost Ninemile Formation, Whiterock Canyon Narrows, Monitor Range, Nye County, Nevada.

Diagnosis. Frontal and preglabellar area long and uninflated; anterior border furrow shallow; anterior bor- der not strongly dorsally inflated; L1 prominent, displaced laterally so glabella bell-shaped in outline; L2 well inflated; glabella with lateral indentation in front of L2 where faint oblique eye ridge runs into axial furrow from anterior part of palpebral lobe; median occipital node prominent; cranidial sculpture of medium sized tubercles; posterior projections prominent, bearing robust and long, posteriorly-directed genal spines; hypostome with ventrally smooth middle body and large, triangular posterior spines; librigena with nearly straight anterior and posterior sections of the facial suture, visual surface set atop independently inflated band of socle; pygidium with four axial rings discernible in most specimens, often with larger pair of tubercles on each ring; pygidium relatively narrow, each posterior pleural band with prominent tubercle at fulcrum.

Discussion. Whittington (1971, p. 456) excluded Protocalymene from his discussion of calymenid taxonomy “because of the difficulty in determining the systematic position of the small specimens on which it is based.” Similarly, Fortey and Droser (1999, p. 197) noted that Ross’s (1967) illustrated material was all “rather small”. This is true, but in light of our new collections it appears that this is because the species reached a diminutive maximum size. Our new silicified collections contain thousands of trilobite sclerites and P. mcallisteri is one of the most common species. The largest cranidia we have recovered are only about 3.3 mm in sagittal length (e.g., Pl. 8, figs 1, 3). There is no reason to suspect the silicified sample is inherently biased toward lack of preservation of larger specimens. Specimens belonging to a species of the pliomerid Ectenonotus Raymond, 1920, for example, are common. Many cranidia of this species have been recovered that are as large or larger than the single calcareous cranidium assigned by Fortey and Droser (1996, fig. 16.3, 16.6, 16.7) to their new E. progenitor. These specimens are more than double the size of the largest P. mcallisteri cranidia. Given that the species are of broadly similar general morphology, it is likely also that hydrodynamic sorting can be ruled out as an explanation for the small maximum size of P. mcallisteri material. Very large illaenid specimens are also common in the collections. Protocalymene mcallisteri appears simply to have been a small trilobite. In addition to the species noted above, Ross (1972, p. 14) listed “ Protocalymene sp.” from the Antelope Valley Formation above the massive bioherm at Meiklejohn Peak, Nye County, Nevada. This occurrence has not been illustrated.

Almost all previous commentators have treated Protocalymene as Calymenidae, and often as Calymeninae (=Flexicalymeninae; see above) (Fortey, 1975, p. 346; Hammann, 1983, p. 46; Fortey, 1990, p. 568; Fortey and Droser, 1999, p. 197; Jell and Adrain, 2003, pp. 431, 468; Loch and Ethington, 2017, p. 310), and as detailed above there has been repeated confusion of Ross’s taxon with the material described by Whittington (1965) in various open nomenclature assignments and formalized here as Atlanticalymene bardensis. The latter, as argued above, is an unambiguous calymenine calymenid. The affinity of Protocalymene is much less clear.A few authors have regarded Protocalymene as of less certain affinity. Kobayashi and Hamada (1977, pp. 124–125), for example, questionably assigned it to a calymenid Subfamily Ptychometopinae Balašova in Černyševa, 1960, along with Ptychometopus Schmidt, 1894, and Endocrania Kobayashi, 1956. Ptychometopus is variably considered either a pharostomatid (e.g., Jell and Adrain, 2003, pp. 436, 476) or a calymenid (e.g., Fortey and Cocks, 2003, p. 267). Endocrania is a junior subjective synonym of the leiostegiid Leiostegium Raymond, 1913 (Zhou and Fortey, 1986, p. 172).

Although it has been regarded as a calymenine, few aspects of the morphology of P. mcallisteri resemble members of this subfamily. In particular, the species has a “normal” preglabellar area and anterior border. In most calymenids, the frontal regions are inflated and the preglabellar field is lost, with a more or less inflated anterior border abutting the front of the glabella. This morphology is reminiscent of that of some species of pharostomatids, such as Pharostoma narinosum Siveter, 1977 (fig. 3A–H). Protocalymene mcallisteri does not appear to be a pharostomatid, however, as species of that group have a posterior facial suture which cuts the anterior border adaxial to the genal spine, with the genal spine positioned on the librigena. In all other calymenoideans the genal spine is on the cranidium, and the posterior facial suture cuts the lateral border, not the posterior border. This is emphatically the case in P. mcallisteri, which has huge genal spines developed on the cranidium. These spines themselves are unusual features in a calymenoidean. Some bathycheilids have large and long genal spines (e.g., Bathycheilus gallicus Dean, 1965) but, again, these are librigenal, not cranidial features.

Protocalymene mcallisteri does not resemble species of Reedocalymeninae or Colpocoryphinae, all of which have prominent adaptations for coaptation which P. mcallisteri entirely lacks.

Despite its unusual morphology, P. mcallisteri has unmistakably calymenoidean features. The rostral plate (Pl. 13, figs 15, 16, 18, 19) is typically calymenoidean, with a border sector and a doublural sector. The hypostome (Pl. 13, figs 1–3) is of typical calymenoidean aspect, with a pair of large posterior spines. The librigena is slightly odd looking due to its nearly straight facial sutures, but it is once again of standard calymenoidean form. In the absence of any obvious close comparisons, but equally obvious calymenoidean affinity, for the time being we elect not to make a family assignment of the genus.

Notes

Published as part of Adrain, Jonathan M., Karim, Talia S. & McAdams, Neo E. B., 2020, Atlanticalymene, a new genus of Middle Ordovician (Darriwilian) calymenine trilobites, and revision of the calymenoidean genus Protocalymene Ross, pp. 1-55 in Zootaxa 4859 (1) on pages 16-17, DOI: 10.11646/zootaxa.4859.1.1, http://zenodo.org/record/4537316

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Linked records

Additional details

Biodiversity

Family
Calymenidae
Genus
Protocalymene
Kingdom
Animalia
Order
Phacopida
Phylum
Arthropoda
Scientific name authorship
Ross
Taxon rank
genus
Type status
holotype
Taxonomic concept label
Protocalymene Ross, 1967 sec. Adrain, Karim & McAdams, 2020

References

  • Ross, R. J., Jr. (1967) Some Middle Ordovician brachiopods and trilobites from the Basin Ranges, western United States. United States Geological Survey Professional Paper, 523 - D, 1 - 43. https: // doi. org / 10.3133 / pp 523 D
  • Ross, R. J., Jr. (1970) Ordovician brachiopods, trilobites, and stratigraphy in eastern and central Nevada. United States Geological Survey Professional Paper, 639, 1 - 103. https: // doi. org / 10.3133 / pp 639
  • Loch, J. D. & Ethington, R. L. (2017) An integrated trilobite and conodont biostratigraphy across the base of the Laurentian Whiterockian Series (lower Middle Ordovician) at its stratotype, Whiterock Canyon Narrows, Nevada. Journal of Paleontology, 91, 294 - 317. https: // doi. org / 10.1017 / jpa. 2016.127
  • Whittington, H. B. (1971) Silurian calymenid trilobites from the United States, Norway and Sweden. Palaeontology, 14, 455 - 477.
  • Fortey, R. A. & Droser, M. L. (1999) Trilobites from the base of the type Whiterockian (Middle Ordovician) in Nevada. Journal of Paleontology, 73, 182 - 201. https: // doi. org / 10.1017 / S 0022336000027712
  • Raymond, P. E. (1920) Some new Ordovician trilobites. Bulletin of the Museum of Comparative Zoology, Harvard, 64, 273 - 296.
  • Fortey, R. A. & Droser, M. L. (1996) Trilobites at the base of the Middle Ordovician, western United States. Journal of Paleontology, 70, 73 - 99. https: // doi. org / 10.1017 / S 002233600002312 X
  • Ross, R. J., Jr. (1972) Fossils from the Ordovician bioherm at Meiklejohn Peak, Nevada. United States Geological Survey Professional Paper, 685, 1 - 47. https: // doi. org / 10.3133 / pp 685
  • Fortey, R. A. (1975) Early Ordovician trilobite communities. Fossils and Strata, 4, 331 - 352.
  • Hammann, W. (1983) Calymenacea (Trilobita) aus dem Ordovizium von Spanien; ihre Biostratigraphie, Okologie und Systematik. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 542, 1 - 177.
  • Fortey, R. A. (1990) Ontogeny, hypostome attachment and trilobite classification. Palaeontology, 33, 529 - 576.
  • Jell, P. A. & Adrain, J. M. (2003) Available generic names for trilobites. Memoirs of the Queensland Museum, 48, 331 - 553.
  • Whittington, H. B. (1965) Trilobites of the Ordovician Table Head Formation, western Newfoundland. Bulletin of the Museum of Comparative Zoology, Harvard, 132, 275 - 442.
  • Kobayashi, T. & Hamada, T. (1977) Devonian trilobites of Japan in comparison with Asian, Pacific and other faunas. Special Papers of the Palaeontological Society of Japan, 20, 1 - 202.
  • Cernyseva, N. E. (1960) [Trilobita]. In: Orlov, U. A. (Ed.), Osnovy paleontologii; spravocnik dla paleontologov i geologov SSSR. 8. Clenistonogie, trilobitoobraznye i rakoobraznye. Akademia Nauk SSSR, Moscow, pp. 17 - 194. [in Russian]
  • Schmidt, F. (1894) Revision der ostbaltischen silurischen Trilobiten. Abteilung IV: Calymmeniden, Proetiden, Bronteiden, Harpeiden, Trinucleiden, Remopleuriden und Agnostiden. Memoires de l'Academie Imperiale des Sciences de St. - Petersbourg, VII'e Serie, 42 (5), 1 - 93.
  • Kobayashi, T. (1956) On the Kaolishaniinae. Japanese Journal of Geology and Geography, 27, 9 - 20.
  • Fortey, R. A. & Cocks, L. R. M. (2003) Palaeontological evidence bearing on global Ordovician-Silurian continental reconstructions. Earth-Science Reviews, 61, 245 - 307. https: // doi. org / 10.1016 / S 0012 - 8252 (02) 00115 - 0
  • Raymond, P. E. (1913) A revision of the species which have been referred to the genus Bathyurus. Bulletin of the Victoria Memorial Museum, 1, 51 - 69. https: // doi. org / 10.4095 / 104944
  • Zhou, Z. - Y. & Fortey, R. A. (1986) Ordovician trilobites from north and northeastern China. Palaeontographica, Abteilung A, 192, 157 - 210.
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