Waptia

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Waptia
Temporal range: Middle Cambrian
Fossil specimens of Waptia
Artist's reconstruction of Waptia fieldensis
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Clade: Mandibulata
Order: Hymenocarina
Genus: Waptia
Walcott, 1912
Species:
W. fieldensis
Binomial name
Waptia fieldensis
Walcott, 1912
Location of the Burgess Shale Formation in British Columbia
Synonyms
  • W. circularis Walcott, 1931

Waptia is an

Middle Cambrian of North America. It grew to a length of 6.65 cm (3 in), and had a large bivalved carapace and a segmented body terminating into a pair of tail flaps. It was an active swimmer and likely a predator of soft-bodied prey. It is also one of the oldest animals with direct evidence of brood care. Waptia fieldensis is the only species classified under the genus Waptia, and is known from the Burgess Shale Lagerstätte of British Columbia, Canada. Specimens of Waptia are also known from the Spence Shale
of Utah, United States.

Based on the number of individuals, Waptia fieldensis is the third most abundant arthropod from the Burgess Shale Formation, with thousands of specimens collected. It was among the first

Charles D. Walcott in 1909. He described it in 1912 and named it after two mountains near the discovery site – Wapta Mountain and Mount Field
.

Although it bears a remarkable resemblance to modern crustaceans, its taxonomic affinities were long unclear. A comprehensive redescription published in 2018 classified it a member of Hymenocarina (which contains numerous other bivalved arthropods) within Mandibulata.

Description

Diagram

Known specimens of Waptia range in length from 13.5 to 66.5 millimetres (0.53 to 2.62 in) with the vast majority (~85%) being 40 to 60 millimetres (1.6 to 2.4 in) long. The bivalved carapace was saddle shaped, and was thin and non mineralised, and was likely flexible in life. The carapace was laterally compressed, and had no distinct boundary between the two halves. The carapace was only attached to the body in a small section near the front of the head. The body was divided into three main segments, the cephalothorax (head), the post-cephalothorax, and the abdomen.

The front of the head bore a pair of reniform (kidney shaped) eyes, about 1 millimetre (0.039 in) across, which were born on short stalks. One specimen with preserved

setae
, which are orientated at an angle of 75° to 95° relative to the antennae axis.

The

endites, particularly on the first pair, which project inward from the legs. The fourth leg differs in the fact that only the very end of the leg is segmented, with the rest being annulated, with the annulated regions being fringed by lamellae
.

The "post-cephalothorax" has 5 segments, associated with 6 somites with corresponding pairs of uniramous annulated appendages, which are fringed with lamellae. The following abdomen is approximately 60% of the total length, with 6 segments and no corresponding legs, which terminates in a forked tail fluke, in which each fluke is composed of three segments.[1]

  • Diagram of the mandibles (light grey) and maxillae (dark grey) of Waptia in side-on (top) and from below (bottom) with the two versions showing movement range of the appendages.
    Diagram of the mandibles (light grey) and maxillae (dark grey) of Waptia in side-on (top) and from below (bottom) with the two versions showing movement range of the appendages.
  • Morphology of the cephalothoracic appendages in side-on view (top) and from the front
    Morphology of the cephalothoracic appendages in side-on view (top) and from the front
  • Post-cephalothorax appendages in side on view (a) with close-up of the tip of the appendage (b) and closeup of the lamellae (c), and a view from below of a sternite with attached appendages
    Post-cephalothorax appendages in side on view (a) with close-up of the tip of the appendage (b) and closeup of the lamellae (c), and a view from below of a sternite with attached appendages

Discovery

Field notebook of Charles D. Walcott (from August 31 to September 3, 1909) detailing the discovery of the Burgess Shale fossils. Three arthropods are drawn in the entry for August 31 – Marrella, Waptia, and Naraoia.[2]
Mount Field with Wapta Mountain in the background, near Field, British Columbia, Canada

Waptia fieldensis was one of the first fossils discovered by

Cyrus West Field.[5]

Taphonomy

Specimens of Waptia fieldensis were recovered from the

Undersea landslides caused by the collapse of parts of the limestone cliff would periodically bury the organisms in the area (as well as organisms carried by the landslides) in fine-grained mud that later became shale.[8]

Based on the number of individuals, Waptia fieldensis constitutes about 2.55% of the total number of organisms recovered from the Burgess Shale, and 0.86% of the

Greater Phyllopod bed.[9] This makes them the third most abundant arthropods of the Burgess Shale (after Marrella and Canadaspis).[4][7] The National Museum of Natural History alone houses more than a thousand specimens of the species from the Burgess Shale.[10] Waptia fieldensis are often found disarticulated, with parts remaining in close proximity to each other.[9]

Specimens of Waptia, referred to as Waptia cf. fieldensis have also found recovered from the Middle Cambrian Spence Shale in Utah, USA.[5][11][12] Some of these specimens are associated with three dimensionally preserved eggs.[13]

Taxonomy

Waptia fieldensis is the only

Waptiidae (established by Walcott in 1912).[10][14]

Some authors suggested that Waptia may be allied to

stem group of crustaceans, or even of all arthropods.[5] Waptia was comprehensively redescribed in 2018, and was placed as part of the clade Hymenocarina within Mandibulata, closely related to Crustacea, due to the clear presence of mandibles and maxillae.[1]

Life restoration of Chuandianella, formerly considered closely related to Waptia, but now considered unrelated.

In 1975, an apparently very similar species was described from the

Maotianshan Shale Lagerstätte of Chengjiang, China. It was originally placed within the "ostracod"-like genus Mononotella, as Mononotella ovata. In 1991, Hou Xian-guang and Jan Bergström reclassified it under the new genus Chuandianella when additional discoveries of more complete specimens made its resemblance to W. fieldensis more apparent. Like W. fieldensis, Chuandianella ovata had a bivalved carapace with a median ridge, a pair of caudal rami, a single pair of antennae, and stalked eyes. In 2004, Jun-Yuan Chen tentatively transferred it to the genus Waptia. However, C. ovata had eight abdominal somites in contrast to five in W. fieldensis. Its limbs were biramous and were undifferentiated, unlike those of W. fieldensis.[10] Other authors deemed these differences to be enough to separate it from Waptia to its own genus.[5][15] In 2022, Chuandianella was redescribed, and was shown to lack mandibles, thus it is probably not closely related to Waptia, despite its similar appearance.[16]

In 2002, a second similar species,

exuviae), and not of the actual animal.[10]

Ecology

Life restoration of Waptia
Animation of Waptia swimming

While historically considered

deposit feeders,[17] feeding by sifting through the sea bottom for edible organic particles,[3] the 2018 re-examination considered Waptia to have been an actively swimming predator of soft-bodied prey items, using its first three pairs of cephalothorax leg-like appendages to capture and manipulate prey, while moving its lamellated appendages in a rhythmic motion to propel itself through the water. Up and down movement of the abdomen and the tail fan was likely used to move vertically within the water column. It may have used the claws on its cephalothoracic leg-like appendages to occasionally rest on surfaces.[1]

In 2015, egg clutches were identified in six specimens from the Burgess Shale. The clutch sizes were small, only containing up to 24 eggs, but each egg was relatively large, with an average diameter of 2 mm (0.079 in). They were attached along the inner surface of the bivalved carapace. Along with

Chengjiang biota (around 7 million years older than the Burgess Shale) which also had fossilized eggs preserved inside the carapace, they constitute the oldest direct evidence of brood care and of K-selection among animals. It indicates that they probably lived in an environment which required them to take special measures to ensure the survival of their young.[18][19][20][21]

See also

References

  1. ^
    PMID 30110460
    .
  2. ^ Smithsonian Institution Archives, Accession 10-166, Walcott, Charles D, (Charles Doolittle), 1850-1927, Charles D. Walcott Collection
  3. ^ .
  4. ^ .
  5. ^ a b c d e "Waptia fieldensis". Royal Ontario Museum. 2011. Retrieved January 14, 2012.
  6. ^ Charles D. Walcott (1912). "Cambrian geology and paleontology II: Middle Cambrian Branchiopoda, Malacostraca, Trilobita, and Merostomata". Smithsonian Miscellaneous Collections. 57 (6): 453–456.
  7. ^ a b Simon Conway Morris (1986). "The community structure of the Middle Cambrian Phyllopod Bed (Burgess Shale)". Palaeontology. 29 (Part 3): 423–467.
  8. .
  9. ^ .
  10. ^ .
  11. ^ "Waptia cf. fieldensis Walcott, 1912". Division of Invertebrate Paleontology, University of Kansas. October 4, 2007. Retrieved January 14, 2012.
  12. S2CID 31568651
    .
  13. .
  14. ^ Mikko Haaramo (October 4, 2007). "Crustaceomorpha – crustaceans and related arthropods". Mikko's Phylogeny Archive. Retrieved January 14, 2012.
  15. ^ Hu-Qin Liu & De-Gan Shu (2004). "New information on Chuandianella from the Lower Cambrian Chengjiang Fauna, Yunnan, China" [澄江化石库中川滇虫属化石的新信息]. Journal of Northwest University (Natural Science Edition) (in Chinese). 34 (4): 453–456.
  16. S2CID 247123967
    .
  17. .
  18. .
  19. .
  20. ^ Emily Chung (18 December 2015). "Burgess Shale fossil Waptia may be oldest mom ever found caring for eggs". CBC News. Retrieved 24 May 2016.
  21. PMID 32426476
    .

External links

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