Amplectobelua

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Amplectobelua
Temporal range: Cambrian Stage 3, 518  Ma [1]
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20191201 Amplectobelua symbrachiata.png
Reconstruction of Amplectobelua symbrachiata
Head carapace, gnathobase-like structures and body flaps of A. symbrachiata.png
Fossil specimen, showing frontal appendages, head carapace, gnathobase-like structures and body flaps
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class:† Dinocaridida
Order:† Radiodonta
Clade:† Amplectobeluidae
Genus:† Amplectobelua
Hou, Bergström & Ahlberg, 1995
Type species
†Amplectobelua symbrachiata
Hou, Bergström & Ahlberg, 1995
Other species
  • †A. stephenensis
    Daley & Budd, 2010

Amplectobelua (meaning "embracing beast") is an extinct genus of late Early Cambrian amplectobeluid radiodont, a group of stem arthropods that mostly lived as free-swimming predators during the first half of the Paleozoic Era.

Contents

Anatomy

Size comparison of two species 20210214 Amplectobelua size comparison.png
Size comparison of two species

Amplectobelua was a giant radiodont, with the largest specimen of A. symbrachiata reaching up to 90 cm (3.0 ft) in body length excluding the frontal appendages and tail. [2] A. stephenensis is much smaller, estimated up to 25 cm (9.8 in) long. [3] The body structures other than frontal appendages are only known from the type species Amplectobelua symbrachiata. Like other radiodonts, Amplectobelua had a pair of jointed frontal appendages, a head covered by dorsal and lateral sclerites (the latter had been misinterpreted as huge eyes [4] ), a limbless body with dorsal gills (setal blades), and a series of flaps on both sides that extended along the length of its body.

Amplectobelua had a specialized frontal appendage, in which it has a distinct 3-segmented shaft region and 12-segmented distal articulated region, and the spine on the fourth segment (first segment of distal articulated region) hooked forward to oppose the tip of the appendage, allowing it to grasp prey like a pincer. Amplectobelua had 11 pairs of body flaps in total, they are relatively elongated and straight in outline. The size of the flaps decrease posteriory, and each of their frontal margin have rows of vein-like structures (strengthening rays). The neck region have at least 3 pairs of slender, reduced anterior flaps. [4] The trunk terminated with a pair of long furcae (streamers).

Amplectobelua shares a unique feature among radiodonts with Ramskoeldia , in having gnathobase-like structures (GLSs) underneath its neck region, at least 6, up to eight. They functioned like the gnathobases of arthropods, being able to rotate and move to shred prey. They were connected to reduced anterior flaps. Additionally, the mouth (oral cone) of Amplectobelua were interpreted as different from typical radiodont, lacking the typical Peytoia -style oral cone and possessing numerous flat tooth-plates with unclear, but possibly non-radial arrangement. [4]

Species

Two species are known, Amplectobelua symbrachiata from the Chengjiang biota and Amplectobelua stephenensis from the later Burgess Shale. [5] A. symbrachiata is known from complete specimens, while A. stephenensis is known only from isolated frontal appendages. A. stephenensis is more advanced, with the frontal appendages being more specialized for grasping: the fourth spine is larger and the spines on outer segments are reduced. A. symbrachiata is previously named as a species of Anomalocaris , Anomalocaris trispinata in 1992, before description of A. symbrachiata. [2] Some studies considered that name Amplectobelua trispinata should be used instead of A. symbrachiata. [6] [7]

Ecology

The movement of the frontal appendages of A. stephenensis 20210812 Amplectobelua stephenensis frontal appendage mobility.gif
The movement of the frontal appendages of A. stephenensis

Amplectobelua was likely nektonic predator. [3] Its frontal appendages were worked like pincers to pinch prey. Its structure was suitable to firmly grasp and manipulate prey to the mouth or tearing off pieces from larges carcasses. [8] Gnathobase-like structures were probably used to chew preys. [4] Research of 432 specimens resulted that it would be an extremely fast-growing animal for an arthropod. [2]

See also

Related Research Articles

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References

  1. ↑ Yang, C.; Li, X.-H.; Zhu, M.; Condon, D. J.; Chen, J. (2018). "Geochronological constraint on the Cambrian Chengjiang biota, South China" (PDF). Journal of the Geological Society. 175 (4): 659–666. Bibcode:2018JGSoc.175..659Y. doi:10.1144/jgs2017-103. ISSN   0016-7649. S2CID   135091168.
  2. 1 2 3 Wu, Yu; Pates, Stephen; Pauly, Daniel; Zhang, Xingliang; Fu, Dongjing (2023-11-03). "Rapid growth in a large Cambrian apex predator". National Science Review. doi: 10.1093/nsr/nwad284 . ISSN   2095-5138. PMC   10833464 .
  3. 1 2 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. Dryad Data
  4. 1 2 3 4 Cong, Peiyun; Daley, A. C.; Edgecombe, Gregory D.; Hou, Xianguang (2017). "The functional head of the Cambrian radiodontan (stem-group Euarthropoda) Amplectobelua symbrachiata". BMC Evolutionary Biology. 17 (208): 208. doi: 10.1186/s12862-017-1049-1 . PMC   5577670 . PMID   28854872.
  5. ↑ Daley, A. C.; Budd, G. E. (2010). "New anomalocaridid appendages from the Burgess Shale, Canada". Palaeontology. 53 (4): 721. Bibcode:2010Palgy..53..721D. doi: 10.1111/j.1475-4983.2010.00955.x .
  6. ↑ Steiner, Michael; Zhu, Maoyan; Zhao, Yuanlong; Erdtmann, Bernd-Dietrich (2005-05-02). "Lower Cambrian Burgess Shale-type fossil associations of South China". Palaeogeography, Palaeoclimatology, Palaeoecology. Interpretation of Biological and Environmental Changes across the Neoproterozoic-Cambrian Boundary. 220 (1): 129–152. doi:10.1016/j.palaeo.2003.06.001. ISSN   0031-0182.
  7. ↑ McCall, Christian R. A. (2023). "A large pelagic lobopodian from the Cambrian Pioche Shale of Nevada". Journal of Paleontology. 97 (5): 1009–1024. doi:10.1017/jpa.2023.63. ISSN   0022-3360.
  8. ↑ De Vivo, Giacinto; Lautenschlager, Stephan; Vinther, Jakob (2021-07-28). "Three-dimensional modelling, disparity and ecology of the first Cambrian apex predators". Proceedings of the Royal Society B: Biological Sciences. 288 (1955): 20211176. doi:10.1098/rspb.2021.1176. ISSN   0962-8452. PMC   8292756 . PMID   34284622.
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