Pahvantia
| Pahvantia Temporal range:
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|---|---|
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| Fossil specimens of Pahvantia hastata | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Order: | †Radiodonta |
| Family: | †Hurdiidae |
| Subfamily: | †Hurdiinae |
| Genus: | †Pahvantia Robison & Richards, 1981 |
| Type species | |
| Pahvantia hastata Robison & Richards, 1981
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Pahvantia is an extinct genus of hurdiid radiodont from the Cambrian period. It is known by a single species, Pahvantia hastata, described from Wheeler Shale and Marjum Formation in Utah.[1] Although it was once considered as a filter feeder based on the large number of putative setae on the frontal appendage, these structures were later interpreted as fossil material of the "trunk" section.
Description
[edit]-
Head sclerites -
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Size estimation
Pahvantia is named after the Pahvant people of western Utah.[2] It was originally described as a possible arthropod of unknown affinity (evolutionary relatives). One specimen was described as a specimen of Proboscicaris agnosta, which was originally interpreted as a bivalved arthropod, but is now considered as the head sclerites of Hurdia.[2][3]
Pahvantia is a relatively small radiodont with an estimated length between 14.4–24 centimetres (5.7–9.4 in).[3] Similar to most other hurdiids, Pahvantia had a large dorsal head sclerite (H-element), and it was more than twice as long than it is wide.[3] Based on the frontal appendage, its morphology is most close to that of Hurdia, although the sclerites' forms are different enough (diagnostic) to consider Pahvantia a distinct genus.[4]
Interpretation of frontal appendage
[edit]Lerosey-Aubril and Pates (2018) considered the fossil specimen KUMIP 314089 as the frontal appendage of the animal, with a multitude of long hair-like structures tentatively interpreted as setae. It was interpreted that frontal appendage had two different types of endites; two proximal short ones with robust, plate-like structures of different widths, and five apparently unpaired endites that are two to three times wider and around three times longer, with anterior margins fringed by numerous setae.[3] However, Moysiuk and Caron (2019) questioned this interpretation, arguing that unnatural fossil preservation against flexibility of structures,[clarification needed] no differentiation between the supposed podomeres and endites interpreted by Lerosey-Aubril and Pates (2018), and what would be much bigger frontal appendages compared to other hurdiids. It was considered that the morphology of the "frontal appendage" shows several bands of lamellae, possibly representing disarticulated endites. Due to preservation status, researchers considered the morphology of the frontal appendage to be uncertain.[5] In 2021, Moysiuk and Caron reinterpreted the morphology of Pahvantia hastata by comparison with Titanokorys; through comparison of the part and counterpart of specimen KUMIP 314089, they found that these actually show a Hurdia-like frontal appendage, with "two proximal short endites with different widths". Lerosey-Aubril and Pates' interpretation (2018) was of one endite and three overlapped endites. The 2021 paper shows that the supposed "five endites with numerous setae" are more comparable to gill blades (setal blades) on the trunk segments.[4]
Palaeoecology
[edit]Pahvantia was originally interpreted as an example of suspension feeding radiodont taxa alongside Aegirocassis and Tamisiocaris, using the numerous setae on frontal appendage to capture microscopic food particles and plankton suspended in the water column.[3][3][6] However, after the morphology of the frontal appendage was reinterpreted, it is now thought that Pahvantia probably had a nekto-benthic lifestyle; it may have captured larger prey living along or in the sediment, similar to what is thought for Hurdia, which had a comparable frontal appendage anatomy.[4]
References
[edit]- ^ Top: counterslab elements overlaid on KUMIP 314089 showing supposed podomeres; Bottom: interpretations of KUMIP 314089; (A) whole fossil as filter-feeding frontal appendage, (B) a shorter Hurdia-like frontal appendage with trunk elements such as setal blades
- ^ Pates S, Lerosey-Aubril R, Daley AC, Kier C, Bonino E, Ortega-Hernández J (2021-01-19). "The diverse radiodont fauna from the Marjum Formation of Utah, USA (Cambrian: Drumian)". PeerJ. 9: e10509. doi:10.7717/peerj.10509. PMC 7821760. PMID 33552709.
- ^ a b Robison RA, Richards BC (January 1981). "Large bivalve arthropods from the middle Cambrian of Utah". University of Kansas Paleontological Contributions. 106: 1–28.
- ^ a b c d e f Lerosey-Aubril R, Pates S (September 2018). "New suspension-feeding radiodont suggests evolution of microplanktivory in Cambrian macronekton". Nature Communications. 9 (1): 3774. Bibcode:2018NatCo...9.3774L. doi:10.1038/s41467-018-06229-7. PMC 6138677. PMID 30218075.
- ^ a b c Caron JB, Moysiuk J (September 2021). "A giant nektobenthic radiodont from the Burgess Shale and the significance of hurdiid carapace diversity". Royal Society Open Science. 8 (9): 210664. Bibcode:2021RSOS....810664C. doi:10.1098/rsos.210664. PMC 8424305. PMID 34527273.
- ^ Moysiuk J, Caron JB (August 2019). "A new hurdiid radiodont from the Burgess Shale evinces the exploitation of Cambrian infaunal food sources". Proceedings. Biological Sciences. 286 (1908): 20191079. doi:10.1098/rspb.2019.1079. PMC 6710600. PMID 31362637.
- ^ Pates S, Daley AC, Butterfield NJ (2019-06-11). "First report of paired ventral endites in a hurdiid radiodont". Zoological Letters. 5 (1): 18. doi:10.1186/s40851-019-0132-4. PMC 6560863. PMID 31210962. Dryad Data Archived 2024-06-07 at the Wayback Machine
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