Titanoprosoma edgecombei, Bicknell & Kimmig & Smith & Scherer, 2024
publication ID |
https://doi.org/10.1206/4008.1 |
persistent identifier |
https://treatment.plazi.org/id/03BA3C03-B20C-FF89-3FFC-FE565F965543 |
treatment provided by |
Felipe (2024-03-04 14:45:04, last updated 2024-03-04 14:51:43) |
scientific name |
Titanoprosoma edgecombei |
status |
gen. et sp. nov. |
Titanoprosoma edgecombei , gen. et sp. nov.
Figures 1–3 View FIGURE 1 View FIGURE 3
centic ( Tollerton, 1989; Anderson and Selden, 1997), with fewer examples of ovate ( Eldredge,
1974; Selden et al., 2019; Lustri et al., 2021) or rounded ( Lustri et al., 2021) shapes. Further, prosomal sections commonly comprise ~30% of the exoskeleton. To date, the combination of an ovate prosoma consisting of half the body length is
FIGURE 2. Proposed reconstruction of Titanoprosoma edgecombei . Image credit: Katrina Kenny.
unknown, distinguishing Titanoprosoma edgecombei , gen. et sp. nov., from other euchelicerates. Nonetheless, comparisons with other Paleozoic euchelicerates are required. The new taxon is distinct from Eurypterida (sea scorpions) as T. edgecombei lacks a demonstrable metasoma, excluding the material from Eurypterida ( Snodgrass, 1952; Dunlop and Lamsdell, 2017). Although SMNK-PAL 1271 is superficially comparable to Xiphosurida (true horseshoe crabs), the lack of an opisthosoma fused into a plate (= thoracetron) excludes the new material from xiphosurids ( Dunlop and Lamsdell, 2017; Bicknell and Pates, 2020; Bicknell et al., 2021). Chasmataspidida is another possibility. However, the lack of a bucklerlike morphology along the opisthosoma ( Marshall et al., 2014; Lamsdell, 2020) and nine postabdominal segments ( Dunlop and Lamsdell, 2017) excludes the Bear Gulch material from the chasmataspidids. We can also consider the synziphosurines ( Bicknell and Pates, 2020)—a paraphyletic assemblage containing basal crown-group euchelicerates ( Giribet and Edgecombe, 2019). Morphologically, T. edgecombei is most comparable to synziphosurine taxa ( Bicknell and Pates, 2020). However, synziphosurine species have at least eight expressed tergites, a pretelson, and lack ovate prosomas. This suggests SMNK-PAL 1271 is not a synziphosurine ( Bergström, 1975; Moore et al., 2005; Dunlop and Lamsdell, 2017). Alternatively, if this animal is a synziphosurine, the morphology is distinct from other forms. Finally, the ovate prosomal morphology contrasts the cooccurring Anderella parva that has a much more crescent-shaped prosoma, excluding SMNK-PAL 1271 from the known Bear Gulch synziphosurine (fig. 4). In sum, SMNK-PAL 1271 is distinct from all other Paleozoic euchelicerates. An additional consideration is that the specimen has a broad, horseshoe shape akin to Lunataspis Rudkin et al., 2008 , followed by the thoracetron and then a pretelson region ( Rudkin et al., 2008; Lamsdell et al., 2023). The holotype does not preserve evidence for these morphologies.
ffle euchelicerate fossil record contains forms that have not been placed within a higherorder grouping due to aberrant morphologies. fflis includes genera such as Bembicosoma Laurie, 1899 , Maldybulakia Tesakov and Alekseev, 1992 , and Offacolus Orr et al., 2000 . We have taken a similarly conservative position in our placement of Titanoprosoma edgecombei within Euchelicerata as the holotype shows seven opisthosomal tergites; a morphology not observed in any marine Paleozoic euchelicerate groups ( Dunlop and Lamsdell, 2017). One conservative perspective is that the additional tergites were telescoped under the large prosoma. However, more material of this rare animal is needed to confirm this assumption and additional specimens are likely to shed more light on the taxonomic position of this species.
One final possibility is that Titanoprosoma edgecombei could belong within Aglaspidida. At least Brachyaglaspis singularis Ortega-Hernández et al., 2016 , shows a larger cephalic region and a reduced number of trunk tergites. However, our material shows no evidence of postventral plates, a morphological characteristic observed in all aglaspidids ( Van Roy, 2005; Ortega-Hernández et al., 2013, 2016; Lerosey-Aubril et al., 2017; Siveter et al., 2018). As such, we can confidently exclude T. edgecombei from Aglaspidida.
Anderson, L. I., and P. A. Selden. 1997. Opisthosomal fusion and phylogeny of Palaeozoic Xiphosura. Lethaia 30: 19 - 31.
Bergstrom, J. 1975. Functional morphology and evolution of xiphosurids. Fossils and Strata 4: 291 - 305.
Bicknell, R. D. C., and S. Pates. 2020. Pictorial atlas of fossil and extant horseshoe crabs, with focus on Xiphosurida. Frontiers in Earth Science 8: 98.
Dunlop, J. A., and J. C. Lamsdell. 2017. Segmentation and tagmosis in Chelicerata. Arthropod Structure and Development 46: 396 - 418.
Eldredge, N. 1974. Revision of the suborder Synziphosurina (Chelicerata, Merostomata), with remarks on merostome phylogeny. American Museum Novitates 2543: 1 - 41.
Giribet, G., and G. D. Edgecombe. 2019. ffle phylogeny and evolutionary history of arthropods. Current Biology 29: R 592 - R 602.
Lamsdell, J. C. 2020. A chasmataspidid affinity for the putative xiphosuran Kiaeria Stormer, 1934. PalZ 94: 449 - 453.
Lamsdell, J. C., P. A. Isotalo, D. M. Rudkin, and M. J. Martin. 2023. A new species of the Ordovician horseshoe crab Lunataspis. Geological Magazine 160: 167 - 171.
Laurie, M. 1899. On a Silurian scorpion and some additional eurypterid remains from the Pentland Hills. Transactions of the Royal Society of Edinburgh 39: 575 - 590.
Lerosey-Aubril, R., J. R. Paterson, S. Gibb, and B. D. Chatterton. 2017. Exceptionally-preserved late Cambrian fossils from the McKay Group (British Columbia, Canada) and the evolution of tagmosis in aglaspidid arthropods. Gondwana Research 42: 264 - 279.
Lustri, L., L. Laibl, and R. D. C. Bicknell. 2021. A revision of Prolimulus woodwardi Fritsch, 1899 with comparison to other paedomorphic belinurids. PeerJ 9: e 10980.
Marshall, D. J., J. C. Lamsdell, E. Shpinev, and S. J. Braddy. 2014. A diverse chasmataspidid (Arthropoda: Chelicerata) fauna from the Early Devonian (Lochkovian) of Siberia. Palaeontology 57: 631 - 655.
Moore, R. A., D. E. G. Briggs, and C. Bartels. 2005. A new specimen of Weinbergina opitzi (Chelicerata: Xiphosura) from the Lower Devonian Hunsruck Slate, Germany. Palaontologische Zeitschrif 79: 399 - 408.
Orr, P. J., D. J. Siveter, D. E. G. Briggs, D. J. Siveter, and M. D. Sutton. 2000. A new arthropod from the Silurian Konservat - Lagerstatte of Herefordshire, UK. Proceedings of the Royal Society of London B, Biological Sciences 267: 1497 - 1504.
Ortega-Hernandez, J., D. A. Legg, and S. J. Braddy. 2013. ffle phylogeny of aglaspidid arthropods and the internal relationships within Artiopoda. Cladistics 29: 15 - 45.
Ortega-Hernandez, J., P. Van Roy, and R. Lerosey-Aubril. 2016. A new aglaspidid euarthropod with a six-segmented trunk from the Lower Ordovician Fezouata Konservat-Lagerstatte, Morocco. Geological Magazine 153: 524 - 536.
Rudkin, D. M., G. A. Young, and G. S. Nowlan. 2008. ffle oldest horseshoe crab: a new xiphosurid from Late Ordovician Konservat-Lagerstatten deposits, Manitoba, Canada. Palaeontology 51: 1 - 9.
Selden, P. A., L. Simonetto, and G. Marsiglio. 2019. An effaced horseshoe crab (Arthropoda: Chelicerata: Xiphosura) from the Upper Carboniferous of the Carnic Alps (Friuli, NE Italy). Rivista Italiana di Paleontologia e Stratigrafia 125: 333 - 342.
Siveter, D. J., R. A. Fortey, X. Zhu, and Z. Zhou. 2018. A three-dimensionally preserved aglaspidid euarthropod with a calcitic cuticle from the Ordovician of China. Geological Magazine 155: 1427 - 1441.
Snodgrass, R. E. 1952. A textbook of arthropod anatomy. Ithaca, NY: Cornell University Press.
Tesakov, A. S., and A. S. Alekseev. 1992. Myriapod-like arthropods from the Lower Devonian of central Kazakhstan. Paleontologicheskii Zhurnal 26: 18 - 23.
Tollerton, V. P. 1989. Morphology, taxonomy, and classification of the order Eurypterida Burmeister, 1843. Journal of Paleontology 63: 642 - 657.
Van Roy, P. 2005. An aglaspidid arthropod from the Upper Ordovician of Morocco with remarks on the affinities and limitations of Aglaspidida. Earth and Environmental Science Transactions of the Royal Society of Edinburgh 96: 327 - 350.
FIGURE 1. Titanoprosoma edgecombei, gen. et sp. nov., holotype from the Bear Gulch Limestone, Carboniferous (Serpukhovian), Montana. (A–C) SMNK-PAL 1271, part. A. Specimen imaged under ethanol and LED light. B. Specimen imaged dry under UV light. C. Interpretative drawing of part showing three main exoskeletal divisions. Numbers indicate expressed tergites. (D–F) SMNK-PAL 1271, counterpart. D. Specimen imaged under ethanol and LED light. E. Specimen imaged dry under UV light. F. Specimen imaged under ethanol and UV light. Abbreviations: app, appendage; dub, doublure. Image credit: Mathias Vielsäcker.
FIGURE 3. SEM micrograph and SEM-EDS elemental maps of Titanoprosoma edgecombei holotype from the Bear Gulch Limestone, Carboniferous (Serpukhovian), Montana. A. SEM micrograph of SMNK-PAL 1271, part. B–I. SEM-EDS elemental maps of Ca, Al, P, Si, Fe, O, Mg, and S, respectively. Scale bar in A applies to all panels.
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