From Wikipedia, the free encyclopedia

Dinocaridida
Temporal range: Cambrian–Early Devonian
Assembly of dinocaridids ( Anomalocaris, Opabinia, Pambdelurion and Kerygmachela)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Dinocaridida
Collins, 1996
Subgroups

Dinocaridida [derivation 1] is a proposed fossil taxon of basal arthropods, [1] which flourished during the Cambrian period and survived up to Early Devonian. Characterized by a pair of frontal appendages and series of body flaps, the name of Dinocaridids ( Greek for deinos "terrible" and Latin for caris "crab") refers to the suggested role of some of these members as the largest marine predators of their time. [1] Dinocaridids are occasionally referred to as the 'AOPK group' by some literatures, [2] [3] [4] as the group compose of Radiodonta ( Anomalocaris and relatives), Opabiniidae ( Opabinia and relatives), and the "gilled lobopodians" Pambdelurion and Kerygmachelidae. [5] It is most likely paraphyletic, with Kerygmachelidae and Pambdelurion more basal than the clade compose of Opabiniidae, Radiodonta and other arthropods. [2] [6] [7]

Anatomy

Eyes (deep blue and black), brain (light blue) and digestive system (yellow) of Radiodonta (left), Kerygmachela (Center) and Opabinia (Right)

Dinocaridids were bilaterally symmetrical, with a mostly non-mineralized cuticle and a body divided into two major groupings of tagmata (body-sections): head and trunk. The head apparently unsegmented [6] [7] and had a pair of specialized frontal appendages just in front of the mouth and eyes. The frontal appendages are either lobopodous (soft as in gilled lobopodians) or arthropodized (hardened and segmented as in Radiodonta) and usually paired, but highly fused into a nozzle-like structure in Opabiniidae. [5] Based on their preocular position and putative protocerebral origin, the frontal appendages are generally thought to be homologous to the labrum of euarthropods and primary antennae of onychophoran, [8] [7] while subsequent evidence also suggest a deutocerebral origin (homologous to the jaws of onychophora and great appendages/ antennae/ chelicerae of euarthropods). [9] [10] The trunk possessed multiple segments, each with its own gill branch and swimming flaps (lobes). [11] It is thought that these flaps moved in an up-and-down motion, in order to propel the animal forward [12] in a fashion similar to the cuttlefish. In gilled lobopodian genera, the trunk may have borne a lobopodous limb (lobopod) underneath each of the flaps. [11] The midgut of dinocaridids had paired digestive glands similar to those of siberiid lobopodians and Cambrian euarthropods. [13] The dinocaridid brain is relatively simple than those of a euarthropod (3-segmented), it is thought to be comprised either 1 (only protocerebrum [8] [14]) or 2 cerebral ganglions (protocerebrum and deutocerebrum). [10]

Classification

Ecdysozoa
Dinocaridida

Although some authors may rather suggest different taxonomic affinities (e.g. as cycloneuralian relatives [15] [5]), most of the phylogenetic studies suggest that dinocaridids are stem group arthropods. [16] [17] [18] [19] [11] [6] [7] [20] [21] [22] Under this scenario, Dinocaridida is a paraphyletic grade in correspond to the arthropod crown group (Euarthropoda or Deuteropoda) and also suggest a lobopodian origin of the arthropod lineage. [23] [6] In general, the gilled lobopodian genera Pambdelurion and Kerygmachela which have lobopodian traits (e.g. lobopodous appendage, annulation) occupied the basal position; while Opabiniidae and Radiodonta are more derived and closely related to the arthropod crown group, with the latter even having significant arthropod affinities such as arthropodization and head sclerites. [22] [24] [6]

In the original description, Dinocaridida was composed of only Opabiniidae and Radiodonta. [1] With the exclusion of questionable taxa (e.g. the putative opabiniid Myoscolex [25]), the former were known only by Opabinia, while all radiodont species were grouped under a single family: Anomalocarididae (hence the previous common name 'Anomalocaridids' [16]). In later studies, the gilled lobopodians Pambdelurion and Kerygmachela were also regarded to be dinocaridids, [5] two new opabiniid genera, Utaurora and Mieridduryn were described, [26] [27] [28] other strange dinocaridids like Parvibellus (which might actually be a juvenile siberiid lobopodian), [29] [27] many radiodonts were reassigned to other new families ( Amplectobeluidae, Tamisiocarididae and Hurdiidae), [19] and a new family, Kerygmachelidae, [27] was named.

Distribution

The group was geographically widespread, and has been reported from Cambrian strata in Canada, United States, Greenland, China, Australia and Russia, [30] as well as the Early to Middle Ordovician of Morocco and Wales [31] [32] [28] and the Early Devonian of Germany. [33]

Notes

  1. ^ Greek for deinos "terrible" and Latin for caris "crab" – sometimes informally spelt Dinocarida, but the second 'id' is linguistically correct – see Hou, Xianguang; Bergström, Jan; Jie, Yang (2006). "Distinguishing anomalocaridids from arthropods and priapulids". Geological Journal. 41 (3–4): 259–269. doi: 10.1002/gj.1050. S2CID  83582128.

References

  1. ^ a b c Collins, D. (1996). "The "Evolution" of Anomalocaris and Its Classification in the Arthropod Class Dinocarida (nov.) and Order Radiodonta (nov.)". Journal of Paleontology. 70 (2): 280–293. Bibcode: 1996JPal...70..280C. doi: 10.1017/S0022336000023362. JSTOR  1306391. S2CID  131622496.
  2. ^ a b Budd, Graham E. (1998). "The morphology and phylogenetic significance of Kerygmachela kierkegaardi Budd (Buen Formation, Lower Cambrian, N Greenland)". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 89 (4): 249–290. doi: 10.1017/S0263593300002418. ISSN  1473-7116. S2CID  85645934.
  3. ^ Liu, Jianni (2004). "A rare lobopod with well-preserved eyes from Chengjiang Lagerstätte and its implications for origin of arthropods". Chinese Science Bulletin. 49 (10): 1063. Bibcode: 2004ChSBu..49.1063L. doi: 10.1360/04wd0052. ISSN  1001-6538.
  4. ^ "Morpho-anatomy of the lobopod Magadictyon cf. haikouensis from the Early Cambrian Chengjiang Lagerstätte, South China". Acta Zoologica. 89 (2): 183. 2008. doi: 10.1111/j.1463-6395.2007.00307.x. ISSN  1463-6395.
  5. ^ a b c d Xianguang, Hou; Jan, Jan Bergström; Jiayu, In Rong; Zongjie, Fang; Zhanghe, Zhou; Renbin, Zhan; Xiangdong, Wang; Xunlai, Yuan; Xianguang, Hou (2006). Dinocaridids – anomalous arthropods or arthropod-like worms?. CiteSeerX  10.1.1.693.5869.
  6. ^ a b c d e Ortega-Hernández, Javier (2016). "Making sense of 'lower' and 'upper' stem-group Euarthropoda, with comments on the strict use of the name Arthropoda von Siebold, 1848". Biological Reviews. 91 (1): 255–273. doi: 10.1111/brv.12168. ISSN  1469-185X. PMID  25528950. S2CID  7751936.
  7. ^ a b c d Ortega-Hernández, Javier; Janssen, Ralf; Budd, Graham E. (2017-05-01). "Origin and evolution of the panarthropod head – A palaeobiological and developmental perspective". Arthropod Structure & Development. Evolution of Segmentation. 46 (3): 354–379. doi: 10.1016/j.asd.2016.10.011. ISSN  1467-8039. PMID  27989966.
  8. ^ a b Cong, Peiyun; Ma, Xiaoya; Hou, Xianguang; Edgecombe, Gregory D.; Strausfeld, Nicholas J. (2014). "Brain structure resolves the segmental affinity of anomalocaridid appendages". Nature. 513 (7519): 538–542. Bibcode: 2014Natur.513..538C. doi: 10.1038/nature13486. ISSN  0028-0836. PMID  25043032. S2CID  4451239.
  9. ^ Zeng, Han; Zhao, Fangchen; Niu, Kecheng; Zhu, Maoyan; Huang, Diying (2020). "An early Cambrian euarthropod with radiodont-like raptorial appendages". Nature. 588 (7836): 101–105. Bibcode: 2020Natur.588..101Z. doi: 10.1038/s41586-020-2883-7. ISSN  1476-4687. PMID  33149303. S2CID  226248177.
  10. ^ a b Moysiuk, Joseph; Caron, Jean-Bernard (2022-08-08). "A three-eyed radiodont with fossilized neuroanatomy informs the origin of the arthropod head and segmentation". Current Biology. 32 (15): 3302–3316.e2. doi: 10.1016/j.cub.2022.06.027. ISSN  0960-9822. PMID  35809569. S2CID  250361698.
  11. ^ a b c Van Roy, Peter; Daley, Allison C.; Briggs, Derek E. G. (2015). "Anomalocaridid trunk limb homology revealed by a giant filter-feeder with paired flaps". Nature. 522 (7554): 77–80. Bibcode: 2015Natur.522...77V. doi: 10.1038/nature14256. ISSN  1476-4687. PMID  25762145. S2CID  205242881.
  12. ^ Usami, Y. (2006). "Theoretical study on the body form and swimming pattern of Anomalocaris based on hydrodynamic simulation". Journal of Theoretical Biology. 238 (1): 11–17. Bibcode: 2006JThBi.238...11U. doi: 10.1016/j.jtbi.2005.05.008. PMID  16002096.
  13. ^ Vannier, Jean; Liu, Jianni; Lerosey-Aubril, Rudy; Vinther, Jakob; Daley, Allison C. (2014-05-02). "Sophisticated digestive systems in early arthropods". Nature Communications. 5 (1): 3641. Bibcode: 2014NatCo...5.3641V. doi: 10.1038/ncomms4641. ISSN  2041-1723. PMID  24785191.
  14. ^ Park, Tae-Yoon S.; Kihm, Ji-Hoon; Woo, Jusun; Park, Changkun; Lee, Won Young; Smith, M. Paul; Harper, David A. T.; Young, Fletcher; Nielsen, Arne T.; Vinther, Jakob (2018-03-09). "Brain and eyes of Kerygmachela reveal protocerebral ancestry of the panarthropod head". Nature Communications. 9 (1): 1019. Bibcode: 2018NatCo...9.1019P. doi: 10.1038/s41467-018-03464-w. ISSN  2041-1723. PMC  5844904. PMID  29523785.
  15. ^ Xian-Guang, Hou; Bergström, Jan; Ahlberg, Per (1995-09-01). "Anomalocaris and other large animals in the lower Cambrian Chengjiang fauna of southwest China". GFF. 117 (3): 163–183. doi: 10.1080/11035899509546213. ISSN  1103-5897.
  16. ^ a b Daley, A. C.; Budd, G. E.; Caron, J.-B.; Edgecombe, G. D.; Collins, D. (2009-03-20). "The Burgess Shale Anomalocaridid Hurdia and Its Significance for Early Euarthropod Evolution". Science. 323 (5921): 1597–1600. Bibcode: 2009Sci...323.1597D. doi: 10.1126/science.1169514. ISSN  0036-8075. PMID  19299617. S2CID  206517995.
  17. ^ Edgecombe, Gregory D. (2010). "Arthropod phylogeny: an overview from the perspectives of morphology, molecular data and the fossil record". Arthropod Structure & Development. 39 (2–3): 74–87. doi: 10.1016/j.asd.2009.10.002. ISSN  1873-5495. PMID  19854297.
  18. ^ Legg, David A.; Sutton, Mark D.; Edgecombe, Gregory D. (2013). "Arthropod fossil data increase congruence of morphological and molecular phylogenies". Nature Communications. 4 (1): 2485. Bibcode: 2013NatCo...4.2485L. doi: 10.1038/ncomms3485. ISSN  2041-1723. PMID  24077329.
  19. ^ a b Vinther, Jakob; Stein, Martin; Longrich, Nicholas R.; Harper, David A. T. (2014). "A suspension-feeding anomalocarid from the Early Cambrian" (PDF). Nature. 507 (7493): 496–499. Bibcode: 2014Natur.507..496V. doi: 10.1038/nature13010. ISSN  1476-4687. PMID  24670770. S2CID  205237459.
  20. ^ Lerosey-Aubril, Rudy; Pates, Stephen (2018-09-14). "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. ISSN  2041-1723. PMC  6138677. PMID  30218075.
  21. ^ Moysiuk, J.; Caron, J.-B. (2019-08-14). "A new hurdiid radiodont from the Burgess Shale evinces the exploitation of Cambrian infaunal food sources". Proceedings of the Royal Society B: Biological Sciences. 286 (1908): 20191079. doi: 10.1098/rspb.2019.1079. PMC  6710600. PMID  31362637.
  22. ^ a b Chipman, Ariel D.; Edgecombe, Gregory D. (2019-10-09). "Developing an integrated understanding of the evolution of arthropod segmentation using fossils and evo-devo". Proceedings of the Royal Society B: Biological Sciences. 286 (1912): 20191881. doi: 10.1098/rspb.2019.1881. PMC  6790758. PMID  31575373.
  23. ^ Budd, G. E. (1996). "The morphology of Opabinia regalis and the reconstruction of the arthropod stem-group". Lethaia. 29: 1–14. doi: 10.1111/j.1502-3931.1996.tb01831.x.
  24. ^ Ortega-Hernández, Javier (2015-06-15). "Homology of Head Sclerites in Burgess Shale Euarthropods". Current Biology. 25 (12): 1625–1631. doi: 10.1016/j.cub.2015.04.034. ISSN  0960-9822. PMID  25959966.
  25. ^ Briggs, Derek E. G.; Nedin, Christopher (1997). "The taphonomy and affinities of the problematic fossil Myoscolex from the Lower Cambrian Emu Bay Shale of South Australia". Journal of Paleontology. 71 (1): 22–32. Bibcode: 1997JPal...71...22B. doi: 10.1017/S0022336000038919. ISSN  0022-3360. S2CID  131851540.
  26. ^ Pates, Stephen; Wolfe, Joanna M.; Lerosey-Aubril, Rudy; Daley, Allison C.; Ortega-Hernández, Javier (2022-02-09). "New opabiniid diversifies the weirdest wonders of the euarthropod stem group". Proceedings of the Royal Society B: Biological Sciences. 289 (1968): 20212093. doi: 10.1098/rspb.2021.2093. PMC  8826304. PMID  35135344.
  27. ^ a b c McCall, C. 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.
  28. ^ a b Pates, S.; Botting, J. P.; Muir, L. A.; Wolfe, J. M. (2022). "Ordovician opabiniid-like animals and the role of the proboscis in euarthropod head evolution". Nature Communications. 13 (1). 6969. Bibcode: 2022NatCo..13.6969P. doi: 10.1038/s41467-022-34204-w. PMC  9666559. PMID  36379946.
  29. ^ Liu, Jianni; Dunlop, Jason A.; Steiner, Michael; Shu, Degan (2022-07-22). "A Cambrian fossil from the Chengjiang fauna sharing characteristics with gilled lobopodians, opabiniids and radiodonts". Frontiers in Earth Science. 10: 861934. doi: 10.3389/feart.2022.861934. ISSN  2296-6463.
  30. ^ Ponomarenko, A. G. (2010). "First record of Dinocarida from Russia". Paleontological Journal. 44 (5): 503–504. doi: 10.1134/S0031030110050047. S2CID  128957999.
  31. ^ Potin, G. J.-M.; Gueriau, P.; Daley, A. C. (2023). "Radiodont frontal appendages from the Fezouata Biota (Morocco) reveal high diversity and ecological adaptations to suspension-feeding during the Early Ordovician". Frontiers in Ecology and Evolution. 11. 1214109. doi: 10.3389/fevo.2023.1214109.
  32. ^ Pates, Stephen; Botting, Joseph P.; McCobb, Lucy M. E.; Muir, Lucy A. (2020). "A miniature Ordovician hurdiid from Wales demonstrates the adaptability of Radiodonta". Royal Society Open Science. 7 (6): 200459. Bibcode: 2020RSOS....700459P. doi: 10.1098/rsos.200459. PMC  7353989. PMID  32742697.
  33. ^ Kühl, G.; Briggs, D. E. G.; Rust, J. (Feb 2009). "A Great-Appendage Arthropod with a Radial Mouth from the Lower Devonian Hunsrück Slate, Germany". Science. 323 (5915): 771–3. Bibcode: 2009Sci...323..771K. doi: 10.1126/science.1166586. ISSN  0036-8075. PMID  19197061. S2CID  47555807.
From Wikipedia, the free encyclopedia

Dinocaridida
Temporal range: Cambrian–Early Devonian
Assembly of dinocaridids ( Anomalocaris, Opabinia, Pambdelurion and Kerygmachela)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Dinocaridida
Collins, 1996
Subgroups

Dinocaridida [derivation 1] is a proposed fossil taxon of basal arthropods, [1] which flourished during the Cambrian period and survived up to Early Devonian. Characterized by a pair of frontal appendages and series of body flaps, the name of Dinocaridids ( Greek for deinos "terrible" and Latin for caris "crab") refers to the suggested role of some of these members as the largest marine predators of their time. [1] Dinocaridids are occasionally referred to as the 'AOPK group' by some literatures, [2] [3] [4] as the group compose of Radiodonta ( Anomalocaris and relatives), Opabiniidae ( Opabinia and relatives), and the "gilled lobopodians" Pambdelurion and Kerygmachelidae. [5] It is most likely paraphyletic, with Kerygmachelidae and Pambdelurion more basal than the clade compose of Opabiniidae, Radiodonta and other arthropods. [2] [6] [7]

Anatomy

Eyes (deep blue and black), brain (light blue) and digestive system (yellow) of Radiodonta (left), Kerygmachela (Center) and Opabinia (Right)

Dinocaridids were bilaterally symmetrical, with a mostly non-mineralized cuticle and a body divided into two major groupings of tagmata (body-sections): head and trunk. The head apparently unsegmented [6] [7] and had a pair of specialized frontal appendages just in front of the mouth and eyes. The frontal appendages are either lobopodous (soft as in gilled lobopodians) or arthropodized (hardened and segmented as in Radiodonta) and usually paired, but highly fused into a nozzle-like structure in Opabiniidae. [5] Based on their preocular position and putative protocerebral origin, the frontal appendages are generally thought to be homologous to the labrum of euarthropods and primary antennae of onychophoran, [8] [7] while subsequent evidence also suggest a deutocerebral origin (homologous to the jaws of onychophora and great appendages/ antennae/ chelicerae of euarthropods). [9] [10] The trunk possessed multiple segments, each with its own gill branch and swimming flaps (lobes). [11] It is thought that these flaps moved in an up-and-down motion, in order to propel the animal forward [12] in a fashion similar to the cuttlefish. In gilled lobopodian genera, the trunk may have borne a lobopodous limb (lobopod) underneath each of the flaps. [11] The midgut of dinocaridids had paired digestive glands similar to those of siberiid lobopodians and Cambrian euarthropods. [13] The dinocaridid brain is relatively simple than those of a euarthropod (3-segmented), it is thought to be comprised either 1 (only protocerebrum [8] [14]) or 2 cerebral ganglions (protocerebrum and deutocerebrum). [10]

Classification

Ecdysozoa
Dinocaridida

Although some authors may rather suggest different taxonomic affinities (e.g. as cycloneuralian relatives [15] [5]), most of the phylogenetic studies suggest that dinocaridids are stem group arthropods. [16] [17] [18] [19] [11] [6] [7] [20] [21] [22] Under this scenario, Dinocaridida is a paraphyletic grade in correspond to the arthropod crown group (Euarthropoda or Deuteropoda) and also suggest a lobopodian origin of the arthropod lineage. [23] [6] In general, the gilled lobopodian genera Pambdelurion and Kerygmachela which have lobopodian traits (e.g. lobopodous appendage, annulation) occupied the basal position; while Opabiniidae and Radiodonta are more derived and closely related to the arthropod crown group, with the latter even having significant arthropod affinities such as arthropodization and head sclerites. [22] [24] [6]

In the original description, Dinocaridida was composed of only Opabiniidae and Radiodonta. [1] With the exclusion of questionable taxa (e.g. the putative opabiniid Myoscolex [25]), the former were known only by Opabinia, while all radiodont species were grouped under a single family: Anomalocarididae (hence the previous common name 'Anomalocaridids' [16]). In later studies, the gilled lobopodians Pambdelurion and Kerygmachela were also regarded to be dinocaridids, [5] two new opabiniid genera, Utaurora and Mieridduryn were described, [26] [27] [28] other strange dinocaridids like Parvibellus (which might actually be a juvenile siberiid lobopodian), [29] [27] many radiodonts were reassigned to other new families ( Amplectobeluidae, Tamisiocarididae and Hurdiidae), [19] and a new family, Kerygmachelidae, [27] was named.

Distribution

The group was geographically widespread, and has been reported from Cambrian strata in Canada, United States, Greenland, China, Australia and Russia, [30] as well as the Early to Middle Ordovician of Morocco and Wales [31] [32] [28] and the Early Devonian of Germany. [33]

Notes

  1. ^ Greek for deinos "terrible" and Latin for caris "crab" – sometimes informally spelt Dinocarida, but the second 'id' is linguistically correct – see Hou, Xianguang; Bergström, Jan; Jie, Yang (2006). "Distinguishing anomalocaridids from arthropods and priapulids". Geological Journal. 41 (3–4): 259–269. doi: 10.1002/gj.1050. S2CID  83582128.

References

  1. ^ a b c Collins, D. (1996). "The "Evolution" of Anomalocaris and Its Classification in the Arthropod Class Dinocarida (nov.) and Order Radiodonta (nov.)". Journal of Paleontology. 70 (2): 280–293. Bibcode: 1996JPal...70..280C. doi: 10.1017/S0022336000023362. JSTOR  1306391. S2CID  131622496.
  2. ^ a b Budd, Graham E. (1998). "The morphology and phylogenetic significance of Kerygmachela kierkegaardi Budd (Buen Formation, Lower Cambrian, N Greenland)". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 89 (4): 249–290. doi: 10.1017/S0263593300002418. ISSN  1473-7116. S2CID  85645934.
  3. ^ Liu, Jianni (2004). "A rare lobopod with well-preserved eyes from Chengjiang Lagerstätte and its implications for origin of arthropods". Chinese Science Bulletin. 49 (10): 1063. Bibcode: 2004ChSBu..49.1063L. doi: 10.1360/04wd0052. ISSN  1001-6538.
  4. ^ "Morpho-anatomy of the lobopod Magadictyon cf. haikouensis from the Early Cambrian Chengjiang Lagerstätte, South China". Acta Zoologica. 89 (2): 183. 2008. doi: 10.1111/j.1463-6395.2007.00307.x. ISSN  1463-6395.
  5. ^ a b c d Xianguang, Hou; Jan, Jan Bergström; Jiayu, In Rong; Zongjie, Fang; Zhanghe, Zhou; Renbin, Zhan; Xiangdong, Wang; Xunlai, Yuan; Xianguang, Hou (2006). Dinocaridids – anomalous arthropods or arthropod-like worms?. CiteSeerX  10.1.1.693.5869.
  6. ^ a b c d e Ortega-Hernández, Javier (2016). "Making sense of 'lower' and 'upper' stem-group Euarthropoda, with comments on the strict use of the name Arthropoda von Siebold, 1848". Biological Reviews. 91 (1): 255–273. doi: 10.1111/brv.12168. ISSN  1469-185X. PMID  25528950. S2CID  7751936.
  7. ^ a b c d Ortega-Hernández, Javier; Janssen, Ralf; Budd, Graham E. (2017-05-01). "Origin and evolution of the panarthropod head – A palaeobiological and developmental perspective". Arthropod Structure & Development. Evolution of Segmentation. 46 (3): 354–379. doi: 10.1016/j.asd.2016.10.011. ISSN  1467-8039. PMID  27989966.
  8. ^ a b Cong, Peiyun; Ma, Xiaoya; Hou, Xianguang; Edgecombe, Gregory D.; Strausfeld, Nicholas J. (2014). "Brain structure resolves the segmental affinity of anomalocaridid appendages". Nature. 513 (7519): 538–542. Bibcode: 2014Natur.513..538C. doi: 10.1038/nature13486. ISSN  0028-0836. PMID  25043032. S2CID  4451239.
  9. ^ Zeng, Han; Zhao, Fangchen; Niu, Kecheng; Zhu, Maoyan; Huang, Diying (2020). "An early Cambrian euarthropod with radiodont-like raptorial appendages". Nature. 588 (7836): 101–105. Bibcode: 2020Natur.588..101Z. doi: 10.1038/s41586-020-2883-7. ISSN  1476-4687. PMID  33149303. S2CID  226248177.
  10. ^ a b Moysiuk, Joseph; Caron, Jean-Bernard (2022-08-08). "A three-eyed radiodont with fossilized neuroanatomy informs the origin of the arthropod head and segmentation". Current Biology. 32 (15): 3302–3316.e2. doi: 10.1016/j.cub.2022.06.027. ISSN  0960-9822. PMID  35809569. S2CID  250361698.
  11. ^ a b c Van Roy, Peter; Daley, Allison C.; Briggs, Derek E. G. (2015). "Anomalocaridid trunk limb homology revealed by a giant filter-feeder with paired flaps". Nature. 522 (7554): 77–80. Bibcode: 2015Natur.522...77V. doi: 10.1038/nature14256. ISSN  1476-4687. PMID  25762145. S2CID  205242881.
  12. ^ Usami, Y. (2006). "Theoretical study on the body form and swimming pattern of Anomalocaris based on hydrodynamic simulation". Journal of Theoretical Biology. 238 (1): 11–17. Bibcode: 2006JThBi.238...11U. doi: 10.1016/j.jtbi.2005.05.008. PMID  16002096.
  13. ^ Vannier, Jean; Liu, Jianni; Lerosey-Aubril, Rudy; Vinther, Jakob; Daley, Allison C. (2014-05-02). "Sophisticated digestive systems in early arthropods". Nature Communications. 5 (1): 3641. Bibcode: 2014NatCo...5.3641V. doi: 10.1038/ncomms4641. ISSN  2041-1723. PMID  24785191.
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