Wikipedia

Dendrobranchiata

Dendrobranchiata is a suborder of decapods, commonly known as prawns. There are 540 extant species in seven families, and a fossil record extending back to the Devonian. They differ from related animals, such as Caridea and Stenopodidea, by the branching form of the gills and by the fact that they do not brood their eggs, but release them directly into the water. They may reach a length of over 330 millimetres (13 in) and a mass of 450 grams (1.0 lb), and are widely fished and farmed for human consumption.

Dendrobranchiata
Temporal range: Famennian–Recent
Penaeus monodon
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Malacostraca
Order: Decapoda
Suborder: Dendrobranchiata
Bate, 1888
Superfamilies and families[1]

Penaeoidea

Aciculopodidae †
Aegeridae †
Aristeidae
Benthesicymidae
Carpopenaeidae †
Penaeidae
Sicyoniidae
Solenoceridae

Sergestoidea

Luciferidae
Sergestidae
Synonyms[2]

Penaeidea Dana, 1852

Shrimp and prawns

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While Dendrobranchiata and Caridea belong to different suborders of Decapoda, they are very similar in appearance, and in many contexts such as commercial farming and fisheries, they are both often referred to as "shrimp" and "prawn" interchangeably. In the United Kingdom, Australia and some other Commonwealth, the word "prawn" is used almost exclusively, while the opposite is the case in North America. The term "prawn" is also loosely used to describe any large shrimp, especially those that come 15 (or fewer) to the pound (such as "king prawns", yet sometimes known as "jumbo shrimp").

Description

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Together with other swimming Decapoda, Dendrobranchiata show the "caridoid facies", or shrimp-like form.[3] The body is typically robust, and can be divided into a cephalothorax (head and thorax fused together) and a pleon (abdomen).[3] The body is generally slightly flattened side-to-side.[3] The largest species, Penaeus monodon, can reach a mass of 450 grams (16 oz) and a length of 336 millimetres (13.2 in).[4]

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Head

The most conspicuous appendages arising from the head are the antennae. The first pair are biramous (having two flagella), except in Luciferidae, and are relatively small.[5] The second pair can be 2–3 times the length of the body and are always uniramous (having a single flagellum).[5] The mouthparts comprise pairs of mandibles, maxillules and maxillae, arising from the head, and three pairs of maxillipeds, arising from the thorax.[6] A pair of stalked eyes points forwards from the head.[7]

Thorax

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The carapace grows from the thorax to cover the cephalothorax, and extends forwards between the eyes into a rostrum.[7] This is only as long as the stalked eyes in Benthesicymidae, Luciferidae and Sergestidae, but considerably longer in Aristeidae.[7]

As well as the three pairs of maxillipeds, the thorax also bears five pairs of pereiopods, or walking legs; the first three of these end in small chelae (pincers).[8] The last two pereiopods are absent in Luciferidae and Acetes, but much longer than the preceding pereiopods in Hymenopenaeus and Xiphopenaeus.[9]

The thoracic appendages carry gills, which are protected beneath the carapace.[10] The gills are typically branched, and so resemble trees, lending the group its scientific name, Dendrobranchiata, from the Greek words δένδρον (dendron, tree) and βράγχια (branchia, gills).[11]

Pleon

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The pleon, or abdomen, is similar in length to the cephalothorax.[12] It has six segments, the first five bearing lamellar pleopods, and the last one bearing uropods.[13] The pleopods are biramous, except in Sicyoniidae, where they are uniramous.[9] The uropods and telson collectively form the tail fan; the uropods are not divided by a diaeresis, as they are in many other decapods.[14] The telson is pointed and is usually armed with four pairs of setae or spines.[14]

Internal anatomy

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Most of the musculature of a prawn is used for bending the pleon, and almost all the space in the pleon is filled by muscle.[15] More than 17 muscles operate each of the pleopods, and a further 16 power the tail fan in the rapid backward movement of the caridoid escape reaction.[16] These muscles, collectively, are the meat for which prawns are commercially fished and farmed.[17]

The nervous system of prawns comprises a dorsal brain, and a ventral nerve cord, connected by two commissures around the oesophagus.[18] The chief sensory inputs are visual input from the eyes, chemoreceptors on the antennae and in the mouth, and mechanoreceptors on the antennae and elsewhere.[19]

The digestive system comprises a foregut, a midgut and a hindgut, and is situated dorsally.[20] The foregut begins at the mouth, passes through the oesophagus, and opens into a sac that contains the grinding apparatus of the gastric mill.[20] The hepatopancreas feeds into the midgut, where digestive enzymes are released, and nutrients taken up.[20] The hindgut forms faecal pellets, which are then passed out through the muscular anus.[21]

The circulatory system is based around a compact, triangular heart, which pumps blood into three main arteries.[22] Excretion is carried out through the gills, and by specialised glands located at the base of the antennae, and is mostly in the form of ammonia.[23]

Life cycle

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Nauplius of an unidentified prawn from the family Penaeidae
 
A juvenile Litopenaeus vannamei (whiteleg prawn)

Prawns may be divided into two groups: those with an open thelycum (female genitalia) and those with a closed thelycum.[24] In the open–thelycum species, mating takes place towards the end of the moulting cycle, and usually at sunset.[25] In closed–thelycum species, mating takes place shortly after moulting, when the exoskeleton is still soft, and usually occurs in the night.[26] Courtship and mating may take up to 3 hours in Penaeus monodon, while in Farfantepenaeus paulensis, mating lasts just 4–5 seconds.[26] Spawning may occur several times during the moulting cycle, and usually occurs at night.[27]

With the exception of Luciferidae, the eggs of prawns are shed directly into the water, rather than being brooded.[28] The eggs hatch into nauplius larvae, which are followed by zoea larvae (initially protozoea, and later mysis) and then a postlarva, before reaching adulthood.[28] The changes between moults are gradual, and so the development is anamorphic rather than metamorphic.[28]

Uniquely among the Decapoda, the nauplii of Dendrobranchiata are free-swimming.[28] There are five to eight naupliar stages.[29] The earlier stages have three pairs of appendages that are used for locomotion – two pairs of antennae and the mandibles. Later stages also have rudiments of other mouthparts, but the nauplius is unable to feed, and only lasts 24 to 68 hours.[28] The body ends at a two-lobed telson, and the beginnings of a carapace emerge at this stage.[29]

There are typically five or six zoea stages in Dendrobranchiata, divided into protozoea and mysis.[28] In the protozoea larvae, the antennae are still used for locomotion, but the mandibles become specialised for mastication.[29] All the thoracic somites (body segments) have formed, and a carapace is present, covering part of the thorax.[29] It is smooth in the family Penaeidae, but bears many spines in the family Solenoceridae.[29] The pleon (abdomen) is unsegmented in the first protozoea, and ends in a bilobed telson, which may be used for cleaning other appendages, or for steering.[29] By the second protozoea, segmentation appears on the pleon,[29] and by the third protozoea, which may also be called the metazoea, the uropods have appeared.[30]

By the mysis stages, the pereiopods (thoracic appendages) start to be used instead of the antennae for locomotion.[30] The larva swims backwards, with its tail upwards, spinning slowly as it goes.[30] The carapace covers most of the segments of the thorax, and claws appear on the first three pereiopods.[30] By the last mysis stage, the beginnings of pleopods have appeared on the first five segments of the abdomen.[30]

The post-larva or juvenile stage is characterised by the use of the pleopods for locomotion.[31] The claws become functional, but the gills are still rudimentary.[31] The telson is narrower and only retains traces of its two-lobed development.[31] Through a series of gradual changes over following moults, the animal takes on its adult form.[31]

Systematics

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Dendrobranchiata were traditionally grouped together with Caridea as "Natantia" (the swimming decapoda), as opposed to the Reptantia (the walking decapods). In 1888, Charles Spence Bate recognised the differences in gill morphology, and separated Natantia into Dendrobranchiata, Phyllobranchiata and Trichobranchiata.[32] Recent analyses using cladistics and molecular phylogenetics recognise Dendrobranchiata as the sister group to all other Decapoda, collectively called Pleocyemata.[33]

The cladogram below shows Dendrobranchiata's placement within the larger order Decapoda, from analysis by Wolfe et al., 2019.[34]


 Decapoda 
     

Dendrobranchiata (prawns)  

 Pleocyemata 

Stenopodidea (boxer shrimp)  

Procarididea

Caridea ("true" shrimp)  

 

 Reptantia 

Achelata (spiny lobsters and slipper lobsters)  

Polychelida (benthic crustaceans)

Astacidea (lobsters and crayfish)  

Axiidea (mud shrimp, ghost shrimp, and burrowing shrimp)

Gebiidea (mud lobsters and mud shrimp)  

Anomura (hermit crabs and allies)  

Brachyura ("true" crabs)  

(crawling / 
walking 
decapods)
 
 


 
Fossil Aeger (Aegeridae)

Before 2010, the earliest known fossil prawns come from rocks in Madagascar of Permo-Triassic age, 250 million years ago.[35][36] In 2010, however, the discovery of Aciculopoda from Famennian–stage rocks in Oklahoma extended the group's fossil record back to 360 million years ago.[37] The best known fossil prawns are from the Jurassic Solnhofen limestones from Germany.[36]

Living prawns are divided among seven families, five in the superfamily Penaeoidea, and two in the Sergestoidea,[2] although molecular evidence disagrees with some aspects of the current classifications.[38] Collectively, these include 540 extant species, and nearly 100 exclusively fossil species.[1] A further two families are known only from fossils.[1]

The cladogram below shows Dendrobranchiata's internal relationships of extant families (excluding Solenoceridae):[34]

Dendrobranchiata


Dendrobranchiata comprises the following superfamilies and families:

Superfamily Penaeoidea Rafinesque-Schmaltz, 1815
† Aciculopodidae Feldmann & Schweitzer, 2010 – a single Famennian species, Aciculopoda mapesi [37]
† Aegeridae Burkenroad, 1963 – two Mesozoic genera: Aeger and Acanthochirana [39]
Aristeidae Wood-Mason, 1891 – 26 extant species in 9 genera, and one fossil genus [40]
Benthesicymidae Wood-Mason, 1891 – 41 species in 4 genera [40]
† Carpopenaeidae Garassino, 1994 – two Cretaceous species of Carpopenaeus [41]
Penaeidae Rafinesque-Schmaltz, 1815 – 216 extant species in 26 genera, and several extinct genera, mostly Mesozoic [42]
Sicyoniidae Ortmann, 1898 – 43 species of Sicyonia [43]
Solenoceridae Wood-Mason, 1891 – 81 species in 9 genera [44]
Superfamily Sergestoidea Dana, 1852
Luciferidae De Haan, 1849 – 7 species in 2 genera
Sergestidae Dana, 1852 – 90 extant species in six genera, and two extinct monotypic genera [45]

Distribution

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The biodiversity of Dendrobranchiata decreases markedly at increasing latitudes; most species are only found in a region between 40° north and 40° south.[46] Some species may occur at higher latitudes. For instance, Bentheogennema borealis is abundant at 57° north in the Pacific Ocean, while collections of Gennadas kempi have been made as far south as 61° south in the Antarctic Ocean.[46]

Ecology and behaviour

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Fish, such as this Argyropelecus hemigymnus, are important predators of juvenile prawns, such as this Sicyonia.

There is a great deal of ecological variation within the suborder Dendrobranchiata. Some species of Sergestidae live in fresh water, but most prawns are exclusively marine.[31] Species of Sergestidae and Benthesicymidae mostly live in deep water, and Solenoceridae species live offshore, while most Penaeidae species live in shallow inshore waters, and Lucifer is planktonic.[31] Some species burrow in mud on the sea floor during the day and emerge at night to feed.[31]

Prawns are "opportunistic omnivores",[47] and their diet can include a range of food items from fine particles to large organisms. These may include fish, chaetognaths, krill, copepods, radiolarians, phytoplankton, nematocysts, ostracods and detritus.[47] Prawns eat less around the time of ecdysis (moulting), probably because of the softness of the mouthparts, and must eat more than usual to compensate, once ecdysis is complete.[47]

Prawns are an attractive food for predators, with a higher energy content than most other invertebrates.[48] The larvae are prey to comb jellies, jellyfish, chaetognaths, fish and other crustaceans (such as mantis shrimp and crabs), and only a tiny proportion survive.[49] Juveniles are targeted by a number of fish, cephalopods and birds; Litopenaeus vannamei juveniles experience 90% mortality in the 6–12 weeks they spend in Mexican lagoons, and this is thought to be due almost entirely to predation.[49] Adult prawns are less susceptible to predation, but can fall prey to some fish.[50]

Economic importance

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Marsupenaeus japonicus (Kuruma prawn) in an aquaculture facility in Taiwan

Dendrobranchiata are of huge economic importance. While in some countries, such as the United States, production is almost entirely through fisheries, other countries have concentrated on aquaculture (shrimp farms), including Ecuador where 95% of production is farmed; some countries produce similar amounts from fisheries and aquaculture, including Mexico, China, India and Indonesia.[51]

Species from the family Aristeidae are important to deep-water fisheries, particularly in the Mediterranean Sea, where Aristaeomorpha foliacea is caught by trawlers.[51] In Brazil, Aristaeomorpha foliacea, Aristaeopsis edwardsiana and Aristeus antillensis are of commercial importance.[51] The shallow-water Penaeidae are of greater importance, however, and the most important species for fisheries is Fenneropenaeus chinensis, with a catch in 2005 of over 100,000 tons.[33]

The most important species for aquaculture are Marsupenaeus japonicus (Kuruma prawn), Fenneropenaeus chinensis (Chinese prawn), Penaeus monodon (giant tiger prawn) and Litopenaeus vannamei (whiteleg prawn).[33]

References

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  1. ^ a b c De Grave et al., 2009
  2. ^ a b Martin & Davis, 2001
  3. ^ a b c Tavares & Martin, 2010, p. 100
  4. ^ Dall, 1990, pp. 3–4
  5. ^ a b Tavares & Martin, 2010, p. 106
  6. ^ Tavares & Martin, 2010, pp. 106–108
  7. ^ a b c Tavares & Martin, 2010, p. 102
  8. ^ Tavares & Martin, 2010, pp. 108–110
  9. ^ a b Tavares & Martin, 2010, p. 110
  10. ^ Tavares & Martin, 2010, pp. 103–105
  11. ^ Tavares & Martin, 2010, p. 103
  12. ^ Tavares & Martin, 2010, p. 105
  13. ^ Tavares & Martin, 2010, pp. 110–111
  14. ^ a b Tavares & Martin, 2010, p. 111
  15. ^ Tavares & Martin, 2010, p. 113
  16. ^ Tavares & Martin, 2010, pp. 113–114
  17. ^ Kanduri & Eckhardt, 2002, p. 42
  18. ^ Tavares & Martin, 2010, p. 114
  19. ^ Tavares & Martin, 2010, pp. 116–118
  20. ^ a b c Tavares & Martin, 2010, p. 118
  21. ^ Tavares & Martin, 2010, pp. 118–119
  22. ^ Tavares & Martin, 2010, p. 120
  23. ^ Tavares & Martin, 2010, pp. 120–121
  24. ^ Tavares & Martin, 2010, p. 125
  25. ^ Tavares & Martin, 2010, pp. 125–126
  26. ^ a b Tavares & Martin, 2010, p. 126
  27. ^ Tavares & Martin, 2010, p. 127
  28. ^ a b c d e f Tavares & Martin, 2010, p. 130
  29. ^ a b c d e f g Tavares & Martin, 2010, p. 131
  30. ^ a b c d e Tavares & Martin, 2010, p. 133
  31. ^ a b c d e f g Tavares & Martin, 2010, p. 134
  32. ^ Tavares & Martin, 2010, p. 99
  33. ^ a b c Tavares & Martin, 2010, p. 137
  34. ^ a b Wolfe, Joanna M.; Breinholt, Jesse W.; Crandall, Keith A.; Lemmon, Alan R.; Lemmon, Emily Moriarty; Timm, Laura E.; Siddall, Mark E.; Bracken-Grissom, Heather D. (24 April 2019). "A phylogenomic framework, evolutionary timeline and genomic resources for comparative studies of decapod crustaceans". Proceedings of the Royal Society B. 286 (1901). doi:10.1098/rspb.2019.0079. PMC 6501934. PMID 31014217.
  35. ^ Crean, 2004
  36. ^ a b Schram et al., 2000
  37. ^ a b Feldmann & Schweitzer, 2010
  38. ^ Ma et al., 2009
  39. ^ Tavares & Martin, 2010, p. 151
  40. ^ a b Tavares & Martin, 2010, p. 152
  41. ^ Tavares & Martin, 2010, pp. 152–153
  42. ^ Tavares & Martin, 2010, p. 153
  43. ^ Tavares & Martin, 2010, p. 154
  44. ^ Tavares & Martin, 2010, p. 155
  45. ^ Tavares & Martin, 2010, p. 156
  46. ^ a b Tavares & Martin, 2010, p. 145
  47. ^ a b c Tavares & Martin, 2010, p. 135
  48. ^ Dall, 1990, p. 357
  49. ^ a b Dall, 1990, p. 358
  50. ^ Dall, 1990, p. 359
  51. ^ a b c Tavares & Martin, 2010, p. 136

Bibliography

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