Phylas: Lobopodia



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Collinsovermis monstruosus

Artistic reconstruction of Collinsovermis monstruosus. Danielle Dufault © ROM

Taxonomy:

Kingdom: Lobopodia
Phylum: Lobopodia
Higher Taxonomic assignment: Order Luolishaniida, Family Collinsovermidae
Species name: Collinsovermis monstruosus
Remarks:

Collinsovermis is one of a variety of lobopodian taxa from the Cambrian, which are early members of the lineage that gave rise to arthropods, and whose only modern survivors are onychophorans (velvet worms) and tardigrades (water bears). Lobopodians characteristically have annulated, unjointed bodies and bear soft limbs after which they are called: the lobopods. Collinsovermis is an armoured member of the Order Luolishaniida, along with forms such as Collinsium and Luolishania from China, or Acinocricus from Utah—together forming the family Collinsovermidae. Luolishaniids are characterized by their thin spines arranged in chevrons and the differentiation of their body into functional regions for suspension-feeding (Caron & Aria 2017, 2020).

Described by: Caron and Aria
Description date: 2020
Etymology:

Collinsovermis – Collins, patronymic, honours its discoverer, Desmond Collins, and vermis is Latin for worm.

monstruosus – From the Latin, in reference to the nickname ‘Collins’ monster’, first introduced by Delle Cave & Simonetta (1991).

Type Specimens: Holotype: ROMIP 52703, Paratypes: ROMIP 52704 and 52705 at the Royal Ontario Museum, Toronto, Canada.
Other species:

Burgess Shale and vicinity: None.
Other deposits: None.

Age & Localities:

Age:
Middle Cambrian, Wuliuan stage, Bathyuriscus-Elrathina Zone of the Burgess Shale Formation (approximately 507 million years old).
Principal localities:

Mount Stephen

History of Research:

Brief history of research:

Collected by a Royal Ontario Museum expedition on Mount Stephen in 1983, the Collinsovermis animal was first revealed, unnamed and undescribed, in the non-peer-reviewed magazine Rotunda (former name of the Royal Ontario Museum Magazine), as a single picture of the holotype, with the caption: “What is it? This new spiny animal (4 cm) with hairy legs has a body plan that has not been seen before.” In 1991, Italian scientists Delle Cave and Simonetta (1991) provided a brief description of the taxon and attempted a reconstruction solely based on the photograph provided by Collins in the Rotunda magazine, coining it the “Collins’ monster”. Despite the lack of name and good documentation, the Collins’ monster have repeatedly featured in studies tackling lobopodian evolution and phylogeny (e.g., Ramsköld & Chen 1998; Budd 2001; Ou et al. 2011; Caron & Aria 2017). It was only in 2020 that the animal was formally named Collinsovermis monstruosus, in honour of Desmond Collins, and fully described based on high resolution pictures of all available material (Caron & Aria 2020).

Description:

Morphology:

Collinsovermis has a plump appearance, with an annulated, unjointed body divided into anterior and posterior regions. The entire dorsum of the body is covered in well-developed spines—three short pairs cover the first three somites (“body segments”) behind the head, while triads of longs spines cover the remaining 10 somites. The anterior region bears 6 pairs of elongate lobopods with thin spines arranged in chevrons, and a small head, as a protrusion bearing a pair of sensory filaments as well as a small dorsal plate and a frontal mouth. The posterior region is made ventrally of 8 pairs of stout annulated lobopods ending in strong, single claws.

Abundance:

Like other lobopodians, Collinsovermis is excessively rare. There are only 3 specimens known, all from the Collins Quarry on Mount Stephen (Fletcher & Collins 2003). They are housed at the Royal Ontario Museum, Department of Natural History.

Maximum Size:
32 mm.

Ecology:

Life habits: Lobopodia
Feeding strategies: Lobopodia
Ecological Interpretations:

Collinsovermis exemplifies suspension-feeding adaptations in lobopodians associated with strongly-developed defensive elements. Like other members of the order Luolishaniidae, and those of the family bearing its name, this animal was using its stout back limbs for anchoring (probably to sponges) and its slender spinose anterior limbs to sieve organic particles or plankton. The long dorsal spines most certainly served as deterrent to predators.

References:

  • BUDD, G. E. 2001. Tardigrades as ‘stem-group arthropods’: The evidence from the Cambrian fauna. Zoologischer Anzeiger, 240, 265–279.
  • CARON, J. and ARIA, C. 2020. The Collins’ monster, a spinous suspension‐feeding lobopodian from the Cambrian Burgess Shale of British Columbia. Palaeontology, 63, 979–994.
  • CARON, J.-B. and ARIA, C. 2017. Cambrian suspension-feeding lobopodians and the early radiation of panarthropods. BMC Evolutionary Biology, 17, 29.
  • DELLE CAVE, L. and SIMONETTA, A. M. 1991. Early Palaeozoic arthropods and problems of arthropod phylogeny; with some notes on taxa of doubtful affinities. In S, S. A. M. C. M. (ed.) The Early Evolution of Metazoa and the Significance of Problematic Taxa. Proceedings of an International Symposium Held at the University of Camerino 27-31 March 1989, Cambridge University Press, 189–244 pp.
  • FLETCHER, T. P. and COLLINS, D. 2003. The Burgess Shale and associated Cambrian formations west of the Fossil Gully Fault Zone on Mount Stephen, British Columbia. Canadian Journal of Earth Sciences, 40, 1823–1838.
  • OU, Q., LIU, J., SHU, D., HAN, J., ZHANG, Z., WAN, X. and LEI, Q. 2011. A rare onychophoran-like lobopodian from the lower Cambrian Chengjiang Lagerstätte. Journal of Paleontology, 85, 587–594.
  • RAMSKÖLD, L. and CHEN, J. Y. 1998. Cambrian lobopodians: morphology and phylogeny. In EDGECOMBE, G. D. (ed.) Arthropod Fossils and Phylogeny, Columbia University Press, New York, 107–150 pp.
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Ovatiovermis cribratus

Artistic reconstruction of Ovatiovermis cribratus. Danielle Dufault © ROM

Taxonomy:

Kingdom: Lobopodia
Phylum: Lobopodia
Higher Taxonomic Assignment: Order Luolishaniida
Species name: Ovatiovermis cribratus
Remarks:

Ovatiovermis is one of a variety of lobopodian taxa from the Cambrian, which are early members of the lineage that gave rise to arthropods, and whose only modern survivors are onychophorans (velvet worms) and tardigrades (water bears). Lobopodians characteristically have annulated, unjointed bodies and bear soft limbs after which they are called: the lobopods. Ovatiovermis groups with Facivermis as a peculiar “unarmoured” lineage within the Order Luolishaniida, notably characterized by their thin spines arranged in chevrons and the differentiation of their body into functional regions for suspension-feeding (Caron & Aria 2017, 2020).

Described by: Caron and Aria
Description date: 2017
Etymology:

Ovatiovermis – from the Latin ovatio (ovation) and vermis (worm) owing to the inferred upward-reaching, limb-waving posture of these animals.
cribratus – from the Latin cribrare, to sieve.

Type Specimens: Holotype ROMIP 52707 and Paratype ROMIP 64006 at the Royal Ontario Museum, Toronto, Canada.
Other species:

Burgess Shale and vicinity: None

Other deposits: None

Age & Localities:

Age:
Middle Cambrian, Wuliuan stage, Bathyuriscus-Elrathina Zone of the Burgess Shale Formation (approximately 507 million years old).
Principal localities:

The Walcott Quarry on Fossil Ridge.

History of Research:

Brief history of research:

Although the first and most complete specimen was discovered in 1994 by one of the ROM expeditions, Ovatiovermis was not described until 2017 by Caron and Aria. The animal served to exemplify suspension-feeding strategies early in panarthropod evolution, and prompted an analysis of the extent and significance of such lifestyle among other lobopodians.

Description:

Morphology:

Ovatiovermis has a worm-like, tubular body divided into three sections: An anterior section with two pairs of very long lobopods bearing thin spines arranges in chevrons and ending in paired claws; a middle section with four pairs of similar but smaller lobopods; and a posterior section with three pairs of very stout lobopods ending in single strong claws. The head is small and bears a pair of simple visual organs and an eversible pharynx. The surface of the body is devoid of any sclerite or spine. Cuticular folds are visible in the space in between lobopods.

Abundance:

Only two specimens. The holotype specimen (ROMIP 52707) was collected in 1994 from bed assemblage −120 (about 1.2 m below the base of the original Walcott Quarry floor), which is distinct from other bed assemblages in that it has particularly well-preserved specimens across a range of taxa (92 species). The paratype specimen (ROMIP 64006) was found in 2016 by a guest on a guided hike to the Walcott Quarry and forwarded to Dr. Jean-Bernard Caron by the Parks Interpreter office.

Maximum Size:
Maximum Size: 25 mm.

Ecology:

Life habits: Lobopodia
Feeding strategies: Lobopodia
Ecological Interpretations:

With its anterior sieving and posterior anchoring appendages, Ovatiovermis exemplifies suspension-feeding specialization among lobopodians. It was likely anchored to sponges and stood erect in the water to catch food particles or plankton.

References:

  • CARON, J. and ARIA, C. 2020. The Collins’ monster, a spinous suspension‐feeding lobopodian from the Cambrian Burgess Shale of British Columbia. Palaeontology, 63, 979–994.
  • CARON, J.-B. and ARIA, C. 2017. Cambrian suspension-feeding lobopodians and the early radiation of panarthropods. BMC Evolutionary Biology, 17, 29.
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Aysheaia pedunculata

Reconstruction of Aysheaia pedunculata.

© Marianne Collins

Taxonomy:

Kingdom: Lobopodia
Phylum: Lobopodia
Higher Taxonomic assignment: None
Species name: Aysheaia pedunculata
Remarks:

Aysheaia is one of a variety of lobopodian taxa from the Cambrian, which are early members of the lineage that gave rise to arthropods, and whose only modern survivors are onychophorans (velvet worms) and tardigrades (water bears). Lobopodians characteristically have annulated, unjointed bodies and bear soft limbs after which they are called: the lobopods. Although the finding is not consensual, the type of claws and orientation of rear limbs suggest that Aysheaia could be the earliest member of the water bear lineage.

Described by: Walcott
Description date: 1911
Etymology:

Genus – after the nearby Aysha peak (since renamed Ayesha peak) in the Wapta icefield (3,065 m); original meaning unknown.

species – from the Latin pedunculus, “foot.”

Type Specimens: Holotype –USNM57655 in the National Museum of Natural History, Smithsonian Institution, Washington, DC, USA.
Other species:

Burgess Shale and vicinity: none

Other deposits: A.? prolata from the Middle Cambrian of Utah (Robison, 1985).

Age & Localities:

Age:
Middle Cambrian, Wuliuan stage, Burgess Shale Formation (approximately 505 million years ago).
Principal localities:

The Walcott Quarry on Fossil Ridge.

History of Research:

Brief history of research:

Walcott originally described Aysheaia as an annelid worm (Walcott 1911). It was later re-described as a velvet worm (or a close relative) (Brues 1923; Walton 1927; Hutchinson 1930; Walcott 1931), although it lacked features such as jaws and slime glands. Certain authors advocated a position in its own phylum (Tiegs & Manton 1958). A morphological reinterpretation based on photographs (Delle Cave & Simonetta 1975) prompted a detailed re-study of the fossil specimens (Whittington 1978), and relationships were suggested with the water bears (tardigrades) (Bergström 1978). Although some more recent phylogenetic approaches resolve Aysheaia as a basal lobopodian (Smith & Ortega-Hernandez 2014; Yang et al. 2015), other find support for a more derived affinity and a close relationship with tardigrades (Caron & Aria 2017, 2020).

Description:

Morphology:

Aysheaia is a worm-like animal, 1 to 6 cm in length and about 5 mm broad, bearing ten pairs of clawed, spiny limbs on the lower part of its body. It did not have a separate head, but a mouth occupied the very front of the body, accompanied by a pair of appendages and a circlet of bumps (papillae). The animal had a soft, flexible, non-mineralized cuticle, which had a corrugated, accordion-like form. Each stubby limb had ten corrugations, some of which bore a spiny projection. The terminal pair of limbs was oriented towards the front of the animal. A suite of claws also adorned the end of each stub-foot. A faint line running down the axis of the organism is interpreted as its gut.

Abundance:

Aysheaia is rare in the Walcott Quarry representing less than 0.04% of the specimens counted in the community (Caron and Jackson, 2008).

Maximum Size:
60 mm

Ecology:

Life habits: Lobopodia
Feeding strategies: Lobopodia
Ecological Interpretations:

Aysheaia is frequently associated with the remains of sponges, and an ecological association has been posited. Considering recent evidence that other lobopodians lived anchored to a substrate for suspension-feeding (Caron & Aria 2017), it is possible that Aysheaia also used sponges as substrate for its lifestyle, although the animal lacked the morphological specializations of a suspension feeder, and more likely grazed or predated walking on their surface.

References:

  • BERGSTRÖM, J. 1978. Morphology of fossil arthropods as a guide to phylogenetic relationships. In Arthropod Phylogeny, Van Nostrand Reinhold Co., New York, 1–56 pp.
  • BRUES, C. 1923. The geographical distribution of the Onychophora. American Naturalist, 57, 210–217.
  • CARON, J. and ARIA, C. 2020. The Collins’ monster, a spinous suspension‐feeding lobopodian from the Cambrian Burgess Shale of British Columbia. Palaeontology, 63, 979–994.
  • CARON, J.-B. and ARIA, C. 2017. Cambrian suspension-feeding lobopodians and the early radiation of panarthropods. BMC Evolutionary Biology, 17, 29.
  • DELLE CAVE, L. and SIMONETTA, A. M. 1975. Notes on the morphology and taxonomic position of Aysheaia (Onycophora?) and of Skania (undetermined phylum). Monitore Zoologico Italiano, (N.S.), 67–81.
  • HUTCHINSON, G. E. 1930. Restudy of some Burgess Shale fossils. Proceedings of the United States National Museum, 78, 59.
  • SMITH, M. R. and ORTEGA-HERNANDEZ, J. 2014. Hallucigenia’s onychophoran-like claws and the case for Tactopoda. Nature, 514, 363–366.
  • TIEGS, O. W. and MANTON, S. M. 1958. The evolution of the Arthropoda. Biological Reviews, 33, 255–333.
  • WALCOTT, C. 1911. Cambrian Geology and Paleontology II. Middle Cambrian annelids. Smithsonian Miscellaneous Collections, 57(5), 109–145.
  • WALCOTT, C. 1931. Addenda to descriptions of Burgess Shale fossils. Smithsonian Miscellaneous Collections, 85(3), 1–46.
  • WALTON, L. B. 1927. The polychaete ancestry of the insects. American Naturalist, 61, 226–250.
  • WHITTINGTON, H. B. 1978. The lobopod animal Aysheaia pedunculata Walcott, Middle Cambrian, Burgess Shale, British Columbia. Philosophical Transactions of the Royal Society of London B, 284, 165–197.
  • YANG, J., ORTEGA-HERNANDEZ, J., GERBER, S., BUTTERFIELD, N. J., HOU, J., LAN, T. and ZHANG, X. 2015. A superarmored lobopodian from the Cambrian of China and early disparity in the evolution of Onychophora. Proceedings of the National Academy of Sciences of the United States of America, 112, 8678–8683.
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