Dendrobranchiata

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").

Together with other swimming Decapoda, Dendrobranchiata show the "caridoid facies", or shrimp-like form.Tavares & Martin, 2010, p. 100 The body is typically robust, and can be divided into a cephalothorax (head and thorax fused together) and a pleon (abdomen). The body is generally slightly flattened side-to-side. The largest species, Penaeus monodon, can reach a mass of {{convert|450|g}} and a length of {{convert|336|mm}}.Dall, 1990, pp. 3–4

File:Shrimp head.jpg

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.Tavares & Martin, 2010, p. 106 The second pair can be 2–3 times the length of the body and are always uniramous (having a single flagellum). The mouthparts comprise pairs of mandibles, maxillules and maxillae, arising from the head, and three pairs of maxillipeds, arising from the thorax.Tavares & Martin, 2010, pp. 106–108 A pair of stalked eyes points forwards from the head.Tavares & Martin, 2010, p. 102

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

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).Tavares & Martin, 2010, pp. 108–110 The last two pereiopods are absent in Luciferidae and Acetes, but much longer than the preceding pereiopods in Hymenopenaeus and Xiphopenaeus.Tavares & Martin, 2010, p. 110

The thoracic appendages carry gills, which are protected beneath the carapace.Tavares & Martin, 2010, pp. 103–105 The gills are typically branched, and so resemble trees, lending the group its scientific name, Dendrobranchiata, from the Greek words {{lang|el|δένδρον}} ({{lang|el|dendron}}, tree) and {{lang|el|βράγχια}} ({{lang|el|branchia}}, gills).Tavares & Martin, 2010, p. 103

The pleon, or abdomen, is similar in length to the cephalothorax.Tavares & Martin, 2010, p. 105 It has six segments, the first five bearing lamellar pleopods, and the last one bearing uropods.Tavares & Martin, 2010, pp. 110–111 The pleopods are biramous, except in Sicyoniidae, where they are uniramous. The uropods and telson collectively form the tail fan; the uropods are not divided by a diaeresis, as they are in many other decapods.Tavares & Martin, 2010, p. 111 The telson is pointed and is usually armed with four pairs of setae or spines.

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.Tavares & Martin, 2010, p. 113 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.Tavares & Martin, 2010, pp. 113–114 These muscles, collectively, are the meat for which prawns are commercially fished and farmed.Kanduri & Eckhardt, 2002, p. 42

The nervous system of prawns comprises a dorsal brain, and a ventral nerve cord, connected by two commissures around the oesophagus.Tavares & Martin, 2010, p. 114 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.Tavares & Martin, 2010, pp. 116–118

The digestive system comprises a foregut, a midgut and a hindgut, and is situated dorsally.Tavares & Martin, 2010, p. 118 The foregut begins at the mouth, passes through the oesophagus, and opens into a sac that contains the grinding apparatus of the gastric mill. The hepatopancreas feeds into the midgut, where digestive enzymes are released, and nutrients taken up. The hindgut forms faecal pellets, which are then passed out through the muscular anus.Tavares & Martin, 2010, pp. 118–119

The circulatory system is based around a compact, triangular heart, which pumps blood into three main arteries.Tavares & Martin, 2010, p. 120 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.Tavares & Martin, 2010, pp. 120–121

File:Shrimp nauplius.jpg of an unidentified prawn from the family Penaeidae]]

File:Penaeus vannamei 01.jpg (whiteleg prawn)]]

Prawns may be divided into two groups: those with an open thelycum (female genitalia) and those with a closed thelycum.Tavares & Martin, 2010, p. 125 In the open-thelycum species, mating takes place towards the end of the moulting cycle, and usually at sunset.Tavares & Martin, 2010, pp. 125–126 In closed-thelycum species, mating takes place shortly after moulting, when the exoskeleton is still soft, and usually occurs in the night.Tavares & Martin, 2010, p. 126 Courtship and mating may take up to 3 hours in Penaeus monodon, while in Farfantepenaeus paulensis, mating lasts just 4–5 seconds. Spawning may occur several times during the moulting cycle, and usually occurs at night.Tavares & Martin, 2010, p. 127

With the exception of Luciferidae, the eggs of prawns are shed directly into the water, rather than being brooded.Tavares & Martin, 2010, p. 130 The eggs hatch into nauplius larvae, which are followed by zoea larvae (initially protozoea, and later mysis) and then a postlarva, before reaching adulthood. The changes between moults are gradual, and so the development is anamorphic rather than metamorphic.

Uniquely among the Decapoda, the nauplii of Dendrobranchiata are free-swimming. There are five to eight naupliar stages.Tavares & Martin, 2010, p. 131 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. The body ends at a two-lobed telson, and the beginnings of a carapace emerge at this stage.

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

By the mysis stages, the pereiopods (thoracic appendages) start to be used instead of the antennae for locomotion.Tavares & Martin, 2010, p. 133 The larva swims backwards, with its tail upwards, spinning slowly as it goes. The carapace covers most of the segments of the thorax, and claws appear on the first three pereiopods. By the last mysis stage, the beginnings of pleopods have appeared on the first five segments of the abdomen.

The post-larva or juvenile stage is characterised by the use of the pleopods for locomotion.Tavares & Martin, 2010, p. 134 The claws become functional, but the gills are still rudimentary. The telson is narrower and only retains traces of its two-lobed development. Through a series of gradual changes over following moults, the animal takes on its adult form.

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.Tavares & Martin, 2010, p. 99 Recent analyses using cladistics and molecular phylogenetics recognise Dendrobranchiata as the sister group to all other Decapoda, collectively called Pleocyemata.Tavares & Martin, 2010, p. 137

The cladogram below shows Dendrobranchiata's placement within the larger order Decapoda, from analysis by Wolfe et al., 2019.{{cite journal |last1=Wolfe |first1=Joanna M. |last2=Breinholt |first2=Jesse W. |last3=Crandall |first3=Keith A. |last4=Lemmon |first4=Alan R. |last5=Lemmon |first5=Emily Moriarty |last6=Timm |first6=Laura E. |last7=Siddall |first7=Mark E. |last8=Bracken-Grissom |first8=Heather D. |url=https://royalsocietypublishing.org/doi/10.1098/rspb.2019.0079 |title=A phylogenomic framework, evolutionary timeline and genomic resources for comparative studies of decapod crustaceans |journal=Proceedings of the Royal Society B | date=24 April 2019 |volume=286 |issue=1901 |doi=10.1098/rspb.2019.0079 |pmid=31014217 |doi-access=free |pmc=6501934 }}

{{Decapoda cladogram}}

File:9150 - Milano - Museo storia naturale - Aeger - Foto Giovanni Dall'Orto 22-Apr-2007 cropped.jpg (Aegeridae)]]

Before 2010, the earliest known fossil prawns come from rocks in Madagascar of Permo-Triassic age, {{Ma|250}}.Crean, 2004Schram et al., 2000 In 2010, however, the discovery of Aciculopoda from Famennian–stage rocks in Oklahoma extended the group's fossil record back to {{Ma|360}}.Feldmann & Schweitzer, 2010 The best known fossil prawns are from the Jurassic Solnhofen limestones from Germany.

Living prawns are divided among seven families, five in the superfamily Penaeoidea, and two in the Sergestoidea, although molecular evidence disagrees with some aspects of the current classifications.Ma et al., 2009 Collectively, these include 540 extant species, and nearly 100 exclusively fossil species.De Grave et al., 2009 A further two families are known only from fossils.

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

{{clade

|style=font-size:85%; line-height:85%

|label1= Dendrobranchiata

|1={{clade

|label1= Sergestoidea

|1={{clade

|1=Luciferidae

|2=Sergestidae }}

|label2= Penaeoidea

|2={{clade

|1={{clade

|1=Sicyoniidae

|2=Penaeidae }}

|2={{clade

|1=Benthesicymidae

|2=Aristeidae }} }} }} }}

Dendrobranchiata comprises the following superfamilies and families:

:Superfamily Penaeoidea Rafinesque-Schmaltz, 1815

::† Aciculopodidae Feldmann & Schweitzer, 2010 – a single Famennian species, Aciculopoda mapesi

::† Aegeridae Burkenroad, 1963 – two Mesozoic genera: Aeger and Acanthochirana Tavares & Martin, 2010, p. 151

::Aristeidae Wood-Mason, 1891 – 26 extant species in 9 genera, and one fossil genus Tavares & Martin, 2010, p. 152

::Benthesicymidae Wood-Mason, 1891 – 41 species in 4 genera

::† Carpopenaeidae Garassino, 1994 – two Cretaceous species of Carpopenaeus Tavares & Martin, 2010, pp. 152–153

::Penaeidae Rafinesque-Schmaltz, 1815 – 216 extant species in 26 genera, and several extinct genera, mostly Mesozoic Tavares & Martin, 2010, p. 153

::Sicyoniidae Ortmann, 1898 – 43 species of Sicyonia Tavares & Martin, 2010, p. 154

::Solenoceridae Wood-Mason, 1891 – 81 species in 9 genera Tavares & Martin, 2010, p. 155

: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 Tavares & Martin, 2010, p. 156

The biodiversity of Dendrobranchiata decreases markedly at increasing latitudes; most species are only found in a region between 40° north and 40° south.Tavares & Martin, 2010, p. 145 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.

File:Messina Straits Argyropelecus hemigymnus.jpg, 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. 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. Some species burrow in mud on the sea floor during the day and emerge at night to feed.

Prawns are "opportunistic omnivores", 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.Tavares & Martin, 2010, p. 135 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.

Prawns are an attractive food for predators, with a higher energy content than most other invertebrates.Dall, 1990, p. 357 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.Dall, 1990, p. 358 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. Adult prawns are less susceptible to predation, but can fall prey to some fish.Dall, 1990, p. 359

File:Marsupenaeus japonicus.jpg (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.Tavares & Martin, 2010, p. 136

Species from the family Aristeidae are important to deep-water fisheries, particularly in the Mediterranean Sea, where Aristaeomorpha foliacea is caught by trawlers. In Brazil, Aristaeomorpha foliacea, Aristaeopsis edwardsiana and Aristeus antillensis are of commercial importance. 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.

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).

{{Reflist|21em}}

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{{Portal|Crustaceans|Arthropods}}

• {{cite web |author=Michael Türkay |year=2011 |title=Dendrobranchiata |publisher=World Register of Marine Species |url=http://www.marinespecies.org/aphia.php?p=taxdetails&id=106669}}
• {{cite web |url=http://www.crustacea.net/crustace/www/dendrobr.htm |title=Dendrobranchiata (Decapoda, Eucarida, Malacostraca) |work=Crustacea, the Higher Taxa |author=J. K. Lowry |publisher=Australian Museum |access-date=2011-06-11 |archive-url=https://web.archive.org/web/20120323014244/http://www.crustacea.net/crustace/www/dendrobr.htm |archive-date=2012-03-23 |url-status=dead }}
• {{cite web |url=http://arthropodgenomes.org/wiki/Dendrobranchiata |archive-url=https://archive.today/20130414060140/http://arthropodgenomes.org/wiki/Dendrobranchiata |url-status=dead |archive-date=2013-04-14 |title=Dendrobranchiata |work=ArthropodBase wiki |author=Arthropod Genomic Consortium }}
• {{Commons category-inline|Dendrobranchiata}}
• {{Wikispecies-inline|Dendrobranchiata}}

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