Erniettomorph

Erniettomorph
Temporal range: late Ediacaran
~567.3–538.8 Ma (Possible Cambrian records)
Examples of members of the Erniettomorpha, with Ernietta top-left, Swartpuntia top-right, and Pteridinium bottom
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: †Petalonamae
Class: †Erniettomorpha
Pflug, 1972
Families

Erniettomorpha is an extinct class, which is commonly considered a part of the phylum Petalonamae, and were around in the late Ediacaran period from 567.3 – 538.8 Ma, with potential records in the lowermost Cambrian of the United States at 518 Ma. They are commonly infaunal in nature, living partially buried within the substrate, and can also be found across the world, excluding the Polar regions and South America. The type genus of the class is Ernietta.

Description

Created in 1972 by Pflug to contain the 13 genera he had split out from the type genus Ernietta, Erniettomorpha is still widely used today for a number of valid taxa. These taxa are commonly constructed of tubular modules arranged in parallel arrays, which then form palisade-like structure. Some genera, such as Pteridinium and Swartpuntia are 'multi-vaned', which means they have more than two lobes, with Pteridinium having three, and Swartpuntia reported with between three to six. Others are noted to be bag-like to lyre-like in shape, such as Ernietta, and Tulaneia respectively. Phyllozoon is notably more simple than all the other genera, being more leaf-like in appearance.

Erniettomorphs are most commonly found in shallow-water marine environments, although they can also be found in deeper waters. They are notably seen being semi endo-benthic/infaunal in nature, where they are partially buried into the substrate. Alongside this, like most other Ediacaran organisms, they do not have an discernable digestive tract, instead feeding via osmosis in the surrounding water, making them osmotrophs. The buried nature of erniettomorphs would also make this lifestyle viable due to the high surface area to volume ratio it required, as the buried parts of the organisms, such as that seen in fossils of Pteridinium, would not need to be metabolically active, allowing them to reduce their metabolic activity enough to make osmotic feeding viable.

Distribution

Erniettomorphs are fairly common around the globe, more so in Africa, although there are no records in South America or the Polar regions They have been found across the Nama Group of Namibia, in the Rawnsley Quartzite of South Australia,, the Inner Meadow site in Newfoundland and Labrador, the Upper Miette Group and Blueflower Formation in Canada, the Ediacaran strata of Wood Canyon Formation in Nevada, the Floyd Church Formation in North Carolina, the Shibantan Member of the Dengying Formation in China, the Ust' Pinega Formation in Russia, Ediacaran strata of the Kushk Series in Iran, and the Podolia region in Ukraine.

There have also been sparse and tentative records of erniettomorphs from the base of the Cambrian period, predominately assigned to Swartpuntia, with the sites being the Cambrian strata of the Wood Canyon Formation in Nevada, the Poleta Formation also in Nevada, and the Uratanna Formation in South Australia. Excluding the potential Australian records, which have been noted to deserve further investigation, due to the terrible preservation of the other Cambrian fossils, some researchers have noted that these could be assignable to other Cambrian frondose organisms.

Taxonomy

Erniettomorpha includes the families Erniettidae and Pteridinidae, as well as genera not assigned to any family, which are as follows:

Family †Erniettidae Pflug, 1972

Family †Pteridinidae Richter, 1955

Unattributed to a family

Due to the simplicity of Phyllozoon, noted in its original description paper, its affinities to the erniettomorphs has been regarded to be tentative, with its erniettomorph-like appearance potentially being a result of this simplicity or convergent evolution. Despite this, the simply appearance of Phyllozoon also makes it difficult to assess any further in-group and/or out-group relationships. Ventogyrus has also been noted to potentially be a part of this class. The genera Inkrylovia and Onegia are also junior synonyms of Pteridinium.

In 1972, Pflug had attempted to propose the erection of new orders, families and subfamilies under the Erniettomorpha class to contain the 13 new genera he had split out from Ernietta. In 1979, Martin Glaessner attempted to make sense of these proposals, only accepting two subfamilies, that being the "Erniettinae" and "Erniobetinae". Eventually, all these proposals would be discounted, with all the 13 new genera being synonymized back into Ernietta by Jenkins et al., 1981. Glassner would also see four families be formally erected for Pflug's described genera in 1979, two of which that are relevant, these being the Erniettidae, first mentioned by Pflug in 1972, and the Pteridinidae, first mentioned by Richter in 1955, which are still used.

See also

References

  1. 1 2 3 Ivantsov, Andrey YU.; Narbonne, Guy M.; Trusler, Peter W.; Greentree, Carolyn; Vickers-Rich, Patricia (October 2016). "Elucidating Ernietta : new insights from exceptional specimens in the Ediacaran of Namibia". Lethaia. 49 (4): 540–554. doi:10.1111/let.12164.
  2. 1 2 3 Runnegar, Bruce; Horodyski, Robert J.; Gehling, James G.; Jensen, Sören; Bengtson, Stefan; Peterson, Kevin J.; Saltzman, Matthew R.; Vendrasco, Michael J. (November 2024). "Tulaneia amabilia n. gen. n. sp.: a new erniettomorph from the Wood Canyon Formation, Nevada and the age of the Ediacaran–Cambrian transition in the Great Basin". Journal of Paleontology. 98 (6): 929–951. doi:10.1017/jpa.2024.45.
  3. 1 2 3 Jenkins, R. J. F.; Gehling, J. G. (1978). "A review of the frond-like fossils of the Ediacara assemblage". Records of the South Australian Museum. 17 (23): 347–359.
  4. 1 2 Evans, Scott D.; Sperling, Erik A.; Lau, Kimberly V.; Strauss, Justin V. (22 May 2026). "Discovery of White Sea assemblage fossils from Laurentia". Science Advances. 12 (21). doi:10.1126/sciadv.aed9916.
  5. 1 2 Xiao, S.; LaFlamme, M. (2009). "On the eve of animal radiation: phylogeny, ecology and evolution of the Ediacara biota". Trends in Ecology & Evolution. 24 (1): 31–40. doi:10.1016/j.tree.2008.07.015. PMID 18952316.
  6. 1 2 Laflamme, M.; Xiao, S.; Kowalewski, M. (2009). "Osmotrophy in modular Ediacara organisms". Proceedings of the National Academy of Sciences. 106 (34): 14438–14443. Bibcode:2009PNAS..10614438L. doi:10.1073/pnas.0904836106. PMC 2732876. PMID 19706530.
  7. ↑ Fedonkin, Mikhail A.; Gehling, James G.; Grey, Kathleen; Narbonne, Guy M.; Vickers-Rich, Patricia (Mar 16, 2007). The Rise of Animals: Evolution and Diversification of the Kingdom Animalia. JHU Press. ISBN 9780801886799. Retrieved May 11, 2022 – via Google Books.
  8. ↑ Gehling, J. G.; García-Bellido, D. C.; Droser, M. L.; Tarhan, M. L.; Runnegar, B. (30 December 2019). "La transición ediacárico-cámbrica: facies sedimentarias versus extinción". Estudios Geológicos. 75 (2): e099. doi:10.3989/egeol.43601.554.
  9. ↑ McIlroy, D.; Denyszyn, S.; Olschewski, P.; Rosse-Guillevic, S.; Muirhead-Hunt, H.; Pérez-Pinedo, D.; McKean, C.; Pasinetti, G.; Rideout, B.; Steele, M.P.; Menon, L.R.; Neville, J.M.; Chida, N.; Taylor, R.S. (29 January 2026). "Ediacaran endlings from the Avalon Assemblage and the severity of the Kotlin Crisis: First documentation of the Inner Meadow Lagerstätte, Newfoundland, Canada". Geology. doi:10.1130/G54217.1.
  10. ↑ Hofmann, Hans J.; Mountjoy, Eric W. (October 2010). "Ediacaran body and trace fossils in Miette Group (Windermere Supergroup) near Salient Mountain, British Columbia". Canadian Journal of Earth Sciences. 47 (10): 1305–1325. doi:10.1139/E10-070.
  11. 1 2 3 4 5 6 Runnegar, Bruce; Gehling, James G.; Jensen, Sören; Saltzman, Matthew R. (October 2024). "Ediacaran paleobiology and biostratigraphy of the Nama Group, Namibia, with emphasis on the erniettomorphs, tubular and trace fossils, and a new sponge, Arimasia germsi n. gen. n. sp". Journal of Paleontology. 98 (S94): 1–59. Bibcode:2024JPal...98S...1R. doi:10.1017/jpa.2023.81.
  12. ↑ Chen, Zhe; Zhou, Chuanming; Xiao, Shuhai; Wang, Wei; Guan, Chengguo; Hua, Hong; Yuan, Xunlai (25 February 2014). "New Ediacara fossils preserved in marine limestone and their ecological implications". Scientific Reports. 4 (1): 4180. Bibcode:2014NatSR...4.4180C. doi:10.1038/srep04180. hdl:10919/74309. PMC 3933909.
  13. ↑ Sokolov, Boris S.; Fedonkin, Mikhail A. (1 March 1984). "The Vendian as the Terminal System of the Precambrian". Episodes. 7 (1): 12–19. doi:10.18814/epiiugs/1984/v7i1/004.
  14. ↑ Vaziri, Seyed Hamid; Majidifard, Mahmoud Reza; Darroch, Simon A.F.; Laflamme, Marc (March 2021). "Ediacaran diversity and paleoecology from central Iran". Journal of Paleontology. 95 (2): 236–251. doi:10.1017/jpa.2020.88.
  15. ↑ Fedonkin, M. A. (1983). "Non-skeletal fauna of Podolia, Dniester River valley". In Velikanov, V. A.; Asseeva, E. A.; Fedonkin, M. A. (eds.). The Vendian of the Ukraine (in Russian). Kiev: Naukova Dumka. pp. 128–139.
  16. 1 2 Hagadorn, James W.; Fedo, Christopher M.; Waggoner, Ben M. (2000). "Early Cambrian Ediacaran-Type Fossils from California". Journal of Paleontology. 74 (4): 731–740. doi:10.1666/0022-3360(2000)074<0731:ECETFF>2.0.CO;2. ISSN 0022-3360. JSTOR 1306951.
  17. ↑ Jensen, Sören; Gehling, James G.; Droser, Mary L. (June 1998). "Ediacara-type fossils in Cambrian sediments". Nature. 393 (6685): 567–569. doi:10.1038/31215. hdl:10662/19945.