Branchiopoda

"Branchiopod" redirects here. Not to be confused with Brachiopod.

Branchiopoda Temporal range: Upper Cambrian–Recent PreꞒ Ꞓ O S D C P T J K Pg N
Clockwise from top left: Artemia (Anostraca), Triops (Notostraca), Daphnia (Cladocera) & Cyzicus (Spinicaudata)
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Arthropoda
Superclass:	Allotriocarida
Class:	Branchiopoda Latreille, 1817
Subclasses
Sarsostraca Tasch, 1969 Phyllopoda Preuss, 1951

Branchiopoda is a class of crustaceans. It comprises fairy shrimp, clam shrimp, Diplostraca (or Cladocera), Notostraca, the Devonian Lepidocaris and possibly the Cambrian Rehbachiella. They are mostly small, freshwater animals that feed on plankton and detritus.

Description

Members of the Branchiopoda are unified by the presence of gills on many of the animals' appendages, including some of the mouthparts. This is also responsible for the name of the group^[1] (from the Ancient Greek: βράγχια, gills, akin to βρόγχος, windpipe; Greek: πούς, foot).^[2] They generally possess compound eyes and a carapace, which may be a shell of two valves enclosing the trunk (as in most Cladocera), broad and shallow (as in the Notostraca), or entirely absent (as in the Anostraca).^[3] In the groups where the carapace prevents the use of the trunk limbs for swimming (Cladocera and clam shrimp), the antennae are used for locomotion, as they are in the nauplius.^[3] Male fairy shrimp have an enlarged pair of antennae with which they grasp the female during mating, while the bottom-feeding Notostraca, the antennae are reduced to vestiges.^[3] The trunk limbs are beaten in a metachronal rhythm, causing a flow of water along the midline of the animal, from which it derives oxygen, food and, in the case of the Anostraca and Notostraca, movement.^[3]

Ecology

Branchiopods are found in continental fresh water, including temporary pools and in hypersaline lakes, and some in brackish water. Only two groups of water fleas include marine species: Family Podonidae in the order Diplostraca, and family Sididae in the order Diplostraca.^[4][5][6] Most branchiopodans eat floating detritus or plankton, which they take using the setae on their appendages.^[3] But notostracans are omnivorous and very opportunistic feeders and will eat algae and bacteria in addition to animals as both predators and scavengers.^[7]

Taxonomy

In early taxonomic treatments, the current members of the Branchiopoda were all placed in a single genus, Monoculus.^[8] The taxon Branchiopoda was erected by Pierre André Latreille in 1817, initially at the rank of order.^[9]

The current upper-level classification of Branchiopoda, according to the World Register of Marine Species (2021), is as follows:^[10]

Class Branchiopoda Latreille, 1817

Subclass Sarsostraca Tasch, 1969

Order Anostraca Sars, 1867

Suborder Anostracina Weekers et al., 2002

Suborder Artemiina Weekers et al., 2002

Subclass Phyllopoda Preuss, 1951

Superorder Diplostraca Gerstaecker, 1866

Order Anomopoda G.O. Sars, 1865

Order Ctenopoda G.O. Sars, 1865

Order Cyclestherida Sars G.O., 1899

Order Haplopoda G.O. Sars, 1865

Order Laevicaudata Linder, 1945

Order Onychopoda G.O. Sars, 1865

Order Spinicaudata Linder, 1945

Order Notostraca G. O. Sars, 1867

Genus †Rehbachiella? Müller, 1983

In addition, the extinct genus Lepidocaris is generally placed in Branchiopoda.

Anostraca

Artemia salina (Anostraca: Artemiidae)

Main article: Anostraca

The fairy shrimp of the order Anostraca are usually 6–25 mm (0.24–0.98 in) long (exceptionally up to 170 mm or 6.7 in).^[11] Most species have 20 body segments, bearing 11 pairs of leaf-like phyllopodia (swimming legs), and the body lacks a carapace.^[12] They live in vernal pools and hypersaline lakes across the world, including pools in deserts, in ice-covered mountain lakes and in Antarctica. They swim "upside-down" and feed by filtering organic particles from the water or by scraping algae from surfaces.^[11] They are an important food for many birds and fish, and are cultured and harvested for use as fish food.^[8] There are 300 species spread across 8 families.^[13]

Lipostraca

Main article: Lepidocaris

Lipostraca contains a single extinct Early Devonian species, Lepidocaris rhyniensis,^[14] which is the most abundant animal in the Rhynie chert deposits.^[15] It resembles modern Anostraca, to which it is probably closely related, although its relationships to other orders remain unclear.^[16] The body is 3 mm (0.12 in) long, with 23 body segments and 19 pairs of appendages, but no carapace.^[17] It occurred chiefly among charophytes, probably in alkaline temporary pools.^[18]

Notostraca

Main article: Notostraca

The order Notostraca comprises the single family Triopsidae, containing the tadpole shrimp or shield shrimp.^[19] The two genera, Triops and Lepidurus, are considered living fossils, having not changed significantly in outward form since the Triassic.^[13] They have a broad, flat carapace, which conceals the head and bears a single pair of compound eyes.^[11] The abdomen is long, appears to be segmented and bears numerous pairs of flattened legs.^[11] The telson is flanked by a pair of long, thin caudal rami.^[3] Phenotypic plasticity within taxa makes species-level identification difficult, and is further compounded by variation in the mode of reproduction.^[13][20] The evidence of phenotypic plasticity of Arctic tadpole shrimp (Lepidurus arcticus, Notostraca) has been observed in Svalbard.^[21] Notostracans are the largest branchiopodans and are omnivores living on the bottom of temporary pools, ponds^[21] and shallow lakes.^[11]

Laevicaudata, Spinicaudata and Cyclestherida (once Conchostraca)

Main article: Clam shrimp

Clam shrimp are bivalved animals which have lived since at least the Devonian. The three groups are not believed to form a clade. They have 10–32 trunk segments, decreasing in size from front to back, and each bears a pair of legs which also carry gills. A strong muscle can close the two halves of the shell together.

Anomopoda, Ctenopoda, Onychopoda, and Haplopoda (once Cladocera)

Daphnia pulex (Cladocera: Daphniidae)

These four orders make up a group of small crustaceans commonly called water fleas. Around 620 species have been recognised so far, with many more undescribed.^[22] They are ubiquitous in inland aquatic habitats, but rare in the oceans.^[11] Most are 0.2–6.0 mm (0.01–0.24 in) long, with a down-turned head, and a carapace covering the apparently unsegmented thorax and abdomen.^[23] There is a single median compound eye.^[11] Most species show cyclical parthenogenesis, where asexual reproduction is occasionally supplemented by sexual reproduction, which produces resting eggs that allow the species to survive harsh conditions and disperse to distant habitats.^[24] In the water bodies of the world, a lot of Cladocera are non-native species, many of which pose a great threat to aquatic ecosystems.^[25]

Evolution

The fossil record of branchiopods extends back at least into the Upper Cambrian and possibly further. The group is thought to be monophyletic, with the Anostraca having been the first group to branch off.^[26] It is thought that the group evolved in the seas, but was forced into temporary pools and hypersaline lakes by the evolution of bony fishes.^[11] Although they were previously considered the sister group to the remaining crustaceans, it is now widely accepted that crustaceans form a paraphyletic group, and Branchiopoda are thought to be sister to a clade comprising Xenocarida (Remipedia and Cephalocarida) and Hexapoda (insects and their relatives).^[27][28]

See also

• Vladicaris

References

1. Georges Cuvier (1851). "Crustacean Entomostraca (Müller)". The animal kingdom: arranged after its organization, forming a natural history of animals, and an introduction to comparative anatomy. Translated by William Benjamin Carpenter. W. S. Orr and co. pp. 434–448.
2. Webster's New World College Dictionary. Cleveland, Ohio: Wiley Publishing. 2010. Archived from the original on October 23, 2016. Retrieved April 20, 2010.
3. Libbie Hyman (1961). "Subclass 1. Branchiopoda". The Invertebrata (4th ed.). Cambridge University Press. pp. 368–375.
4. Sol Felty Light (1970). "Phylum Arthropoda". Intertidal invertebrates of the central California coast. University of California Press. pp. 112–210. ISBN 978-0-520-00750-5.
5. Marine Biology: A Functional Approach to the Oceans and their Organisms
6. Biology of Cladocera: Proceedings of the Second International Symposium on Cladocera
7. Brostoff, Wn; Holmquist, Jg; Schmidt-Gengenbach, J; Zimba, Pv (2010). "Fairy, tadpole, and clam shrimps (Branchiopoda) in seasonally inundated clay pans in the western Mojave Desert and effect on primary producers". Saline Systems. 6 (1): 11. doi:10.1186/1746-1448-6-11. ISSN 1746-1448. PMC 3019125. PMID 21143855.
8. J. M. Melack (2009). "Saline and soda lakes". In Sven Erik Jørgensen (ed.). Ecosystem Ecology. Academic Press. pp. 380–384. ISBN 978-0-444-53466-8.
9. Pierre André Latreille (1831). Georges Cuvier (ed.). The Crustacea, Arachnides and Insecta. The animal kingdom arranged in conformity with its organization. Vol. 3. Henry M'Murtrie (trans.). G. & C. & H. Carvill.
10. "Branchiopoda". WoRMS, World Register of Marine Species. Retrieved 2021-11-24.
11. Denton Belk (2007). "Branchiopoda". In Sol Felty Light; James T. Carlton (eds.). The Light and Smith Manual: Intertidal Invertebrates from Central California to Oregon (4th ed.). University of California Press. pp. 414–417. ISBN 978-0-520-23939-5.
12. D. R. Khanna (2004). "Segmentation in arthropods". Biology of Arthropoda. Discovery Publishing House. pp. 316–394. ISBN 978-81-7141-897-8.
13. Luc Brendonck; D. Christopher Rogers; Jorgen Olesen; Stephen Weeks; Walter R. Hoch (2008). "Global diversity of large branchiopods (Crustacea: Branchiopoda) in freshwater". Hydrobiologia. 595 (1): 167–176. doi:10.1007/s10750-007-9119-9. S2CID 46608816.
14. Paul Selden & John R. Nudds (2004). "The Rhynie Chert". Evolution of Fossil Ecosystems (2nd ed.). Manson Publishing. pp. 47–58. ISBN 978-1-84076-041-5.
15. "Introduction to Branchiopoda". University of California, Berkeley. Retrieved August 5, 2011.
16. Frederick R. Schram; Stefan Koenemann (2001). "Developmental genetics and arthropod evolution: part I, on legs". Evolution & Development. 3 (5): 343–354. doi:10.1046/j.1525-142X.2001.01038.x. PMID 11710766. S2CID 25997101.
17. D. J. Scourfield (1926). "On a new type of crustacean from the old Red Sandstone (Rhynie chert Bed, Aberdeenshire) – Lepidocaris rhyniensis, gen. et sp. nov". Philosophical Transactions of the Royal Society B: Biological Sciences. 214 (411–420): 153–187. Bibcode:1926RSPTB.214..153S. doi:10.1098/rstb.1926.0005. JSTOR 92140.
18. "Lepidocaris". The Rhynie Chert Crustaceans. University of Aberdeen. Retrieved August 5, 2011.
19. J. K. Lowry (October 2, 1999). "Notostraca (Branchiopoda)". Crustacea, the Higher Taxa: Description, Identification, and Information Retrieval. Archived from the original on July 23, 2011. Retrieved February 7, 2011.
20. Lakka, Hanna-Kaisa (2015). "Description of the male Lepidurus arcticus (Branchiopoda: Notostraca) and the potential role of cannibalism in defining male form and population sex ratio". Journal of Crustacean Biology. 35 (3): 319–329. doi:10.1163/1937240X-00002324. S2CID 83523163.
21. Lakka, Hanna-Kaisa (2013). The ecology of a freshwater crustacean : Lepidurus arcticus (Brachiopoda; Notostraca) in a High Arctic region (master's thesis). University of Helsinki. p. 151.
22. L. Forró; N. M. Korovchinsky; A. A. Kotov; A. Petrusek (2008). "Global diversity of cladocerans (Cladocera; Crustacea) in freshwater" (PDF). Hydrobiologia. 595 (1): 177–184. doi:10.1007/s10750-007-9013-5. S2CID 45363782. Archived (PDF) from the original on 2022-10-09.
23. Douglas Grant Smith & Kirstern Work (2001). "Cladoceran Branchiopoda (water fleas)". In Douglas Grant Smith (ed.). Pennak's Freshwater Invertebrates of the United States: Porifera to Crustacea (4th ed.). John Wiley and Sons. pp. 453 488. ISBN 978-0-471-35837-4.
24. Ellen Decaestecker; Luc De Meester; Joachim Mergaey (2009). "Cyclical Parthenogenesis in Daphnia: Sexual Versus Asexual Reproduction". In Isa Schön; Koen Martens; Peter van Dijk (eds.). Lost Sex: The Evolutionary Biology of Parthenogenesis. Springer. pp. 295–316. doi:10.1007/978-90-481-2770-2_15. ISBN 978-90-481-2769-6. S2CID 82949264.
25. Kotov, Alexey A.; Karabanov, Dmitry P.; Van Damme, Kay (2022-09-09). "Non-Indigenous Cladocera (Crustacea: Branchiopoda): From a Few Notorious Cases to a Potential Global Faunal Mixing in Aquatic Ecosystems". Water. 14 (18): 2806. doi:10.3390/w14182806. ISSN 2073-4441.
26. Joel W. Martin & George E. Davis (2001). An Updated Classification of the Recent Crustacea (PDF). Natural History Museum of Los Angeles County. pp. 1–132.
27. David R. Andrew (2011). "A new view of insectecrustacean relationships II. Inferences from expressed sequence tags and comparisons with neural cladistics". Arthropod Structure & Development. 40 (3): 289–302. Bibcode:2011ArtSD..40..289A. doi:10.1016/j.asd.2011.02.001. PMID 21315832.
28. Bjoern M. von Reumont; Ronald A. Jenner; Matthew A. Wills; Emiliano Dell'Ampio; Günther Pass; Ingo Ebersberger; Benjamin Meyer; Stefan Koenemann; Thomas M. Iliffe; Alexandros Stamatakis; Oliver Niehuis; Karen Meusemann; Bernhard Misof (2012). "Pancrustacean phylogeny in the light of new phylogenomic data: support for Remipedia as the possible sister group of Hexapoda" (PDF proofs). Molecular Biology and Evolution. 29 (3): 1031–1045. doi:10.1093/molbev/msr270. PMID 22049065.