Stomiiformes
Stomiiformes | |
---|---|
Astronesthes similus (Phosichthyoidei: Stomiidae) | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Actinopterygii |
Superorder: | Osmeromorpha |
Order: | Stomiiformes Regan, 1909 |
Suborders | |
Synonyms | |
Stomiatiformes |
Stomiiformes is an order of deep-sea ray-finned fishes of very diverse morphology. It includes, for example, dragonfishes, lightfishes (Gonostomatidae and Phosichthyidae), loosejaws, marine hatchetfishes and viperfishes. The order contains 4 families (5 according to some authors) with more than 50 genera and at least 410 species. As usual for deep-sea fishes, there are few common names for species of the order, but the Stomiiformes as a whole are often called dragonfishes and allies or simply stomiiforms.[1]
The scientific name means "Stomias-shaped", from Stomias (the type genus) + the standard fish order suffix "-formes". It ultimately derives from Ancient Greek stóma (στόμᾶ, "mouth") + Latin forma ("external form"), the former in reference to the huge mouth opening of these fishes.[2]
Description and ecology
Members of this order are mostly pelagic fishes living in deep oceanic waters. Their distribution around the world's oceans is very wide, ranging from subtropical and temperate waters up to subarctic or even Antarctic ones. [3]
The smallest species of this order is the bristlemouth Cyclothone pygmaeae. Native to the Mediterranean Sea, it reaches just 1.5 cm (0.6 in) as an adult. The largest species is the barbeled dragonfish Opostomias micripnis, widely found in the Atlantic, Indian and Pacific Oceans and measuring about 50 cm (20 in) in adult length.
These fish have a highly unusual and often almost nightmarish appearance. They all have teeth on the premaxilla and maxilla. Their maxillary ligaments, as well as some muscles and certain bones in the branchial cavity, are specialized in a distinctive way. Most have large mouths extending back past the eyes. Some also have a chin barbel. The dorsal and/or pectoral fins are missing in some, but others have an adipose fin. The pelvic fin has 4-9 rays, and the stomiiformes possess 5-24 branchiostegal rays. Their scales are cycloid, delicate and easily sloughed off; some are scaleless. The coloration is typically dark brown or black; a few (mostly Gonostomatoidei) are silver, and photophores (light-producing organs) are common in this order.[3]
The teeth of stomiiformes are often transparent and non-reflective so that prey will be unlikely to see them in the light generated by bioluminescence. Research has revealed that the transparency of the teeth of Aristostomias scintillans is due to nanoscale structures composed hydroxyapatite and collagen and a lack dentin tubules[4], however a study from a decade prior had shown the teeth of Chauliodus sloani (which are also transparent) have dentin tubules.[5] The reason behind difference in presence of dentin tubules in two species of the same family (Stomiidae) has yet to be addressed.
Bioluminescence
As common for deep-sea creatures, all members of Stomiiformes (except one) have photophores, whose structure is characteristic of the order. The light emitted can be more or less strong and its color can be light yellow, white, violet or red. The light coming from these fish is generally invisible to their prey. The lighting mechanism can be very simple – consisting of small gleaming points on the fish body – or very elaborate, involving lenses and refractors.
The most common arrangement is one or two rows of photophores on the ventral aspect of the body. The rows run from the head down to the tip of the tail. Photophores are also present in chin barbels of the family Stomiidae. The light produced in these glandular organs is the product of an enzymatic reaction, a catylization of coelenterazine by calcium ions.[citation needed][6]
Daily migration
During the day, Stomiiformes stay in deep waters. When the sun sets, most of them follow the dimming sunlight up to near-surface waters, which are richer in animal life such as small fishes and planktonic invertebrates. During the night, these Stomiiformes hunt and feed on such organisms, swimming back to deeper waters when the sun rises. They apparently are able to measure the intensity of the sunlight that reaches them.[citation needed] They will thus move to stay always in the zone where light intensity is very low, though it is not entirely dark.
This daily migration is well observed in quite a few species of stomiiforms. However, it is also performed by other fishes, while some larger Stomiiformes – among them the largest predators of the deep sea – stay in their habitat all the time and feed on smaller migrating fish that return from the surface.
Reproduction
Stomiiforms spawn generally in deep seas, but the eggs are light and float towards the ocean surface. They hatch in surface waters. When the larvae have completed their metamorphosis and look like adults, they descend to join the main population.[citation needed]
Like many benthic fish species, certain members of the order – especially in the genera Cyclothone and Gonostoma – change their sex during their life. When they become sexually mature, they are males; later on they transform into females.[citation needed]
Systematics
The Stomiiformes are often placed in the teleost superorder Stenopterygii, usually together with the Ateleopodiformes (jellynoses), but sometimes on their own. Whether it is indeed justified to accept such a small group is doubtful; it may well be that the closest living relatives of the "Stenopterygii" are found among the superorder Protacanthopterygii, and that the former would need to be merged in the latter. In some classifications, the "Stenopterygii" are kept separate but included with the Protacanthopterygii and the monotypic superorder Cyclosquamata in an unranked clade called Euteleostei. That would probably require splitting two additional monotypic superorders out of the Protacanthopterygii, and thus result in a profusion of very small taxa.[7]
The Stomiiformes have also been considered close relatives of the Aulopiformes. The latter are otherwise placed in a monotypic superorder "Cyclosquamata" but also appear to be quite close to the Protacanthopterygii indeed. The relationships of these – and the Lampriformes or Myctophiformes, which are also usually treated as monotypic superorders – to the taxa mentioned before is still not well resolved at all, and regardless whether one calls them Protacanthopterygii sensu lato or Euteleostei, the phylogeny of this group of moderately-advanced Teleostei is in need of further study.[8]
The ancestral Stomiiformes probably had thin brownish bodies, rows of egg-shaped photophores adorning the lower body parts, and mouths with numerous teeth. From these, two lineages evolved, probably some time during the Late Cretaceous: Among the modern Stomiiformes, the Gonostomatidae and Phosichthyidae are phenetically very similar, but this is due to their being very plesiomorphic and retaining many traits of the original stomiiforms. Each of the two has characteristic synapomorphies with one of the more advanced stomiiform families – the Sternoptychidae and the Stomiidae, respectively. These two, in turn, are highly autapomorphic, and at a casual glance do not look as if they were as closely related to the other stomiiforms as they actually are.
Thus, the classification of the suborders and families of the Stomiiformes is:
- Suborder Gonostomatoidei
- Family Gonostomatidae – bristlemouths, anglemouths, "lightfishes" (including Diplophidae)
- Family Sternoptychidae – marine hatchetfishes, bottlelights, constellationfishes, pearlsides
- Suborder Phosichthyoidei
- Family Phosichthyidae – lightfishes
- Family Stomiidae – barbeled dragonfishes, loosejaws, stareaters
Timeline of genera
Footnotes
- ^ Nelson (2006): pp.207-208
- ^ Woodhouse (1910), Glare (1968-1982), FishBase (2005)
- ^ a b FishBase (2005), Nelson (2006): p.207
- ^ Velasco-Hogan, Audrey; Deheyn, Dimitri; Koch, Marcus; et al. (2019). "On the Nature of the Transparent Teeth of the Deep-Sea Dragonfish, Aristostomias scintillans". Matter. 11: 235–249. doi:10.1016/j.matt.2019.05.010.
- ^ Greven, Hartmut; Walker, Yasmin; Zanger, Klaus (2009). "On the structure of teeth in the viperfish Chauliodus sloani Bloch & Schneider, 1801 (Stomiidae)". Bulletin of Fish Biology. 1 (1/2): 87–98.
- ^ Haddock, Steven; Moline, Mark; Case, James (2010). "Bioluminescence in the Sea". Annual Review of Marine Science. 2: 443–493. doi:10.1146/annurev-marine-120308-081028. PMID 21141672 – via Annual Reviews.
- ^ Nelson (2006): pp.207-208, Diogo (2008)
- ^ FishBase (2005), Diogo (2008)
References
- Diogo, Rui (2008): On the cephalic and pectoral girdle muscles of the deep sea fish Alepocephalus rostratus, with comments on the functional morphology and phylogenetic relationships of the Alepocephaloidei (Teleostei). Anim. Biol. 58(1): 23-29. doi:10.1163/157075608X303636
- FishBase (2005): Order Stomiiformes. Version of 2005-FEB-15. Retrieved 2009-SEP-28.
- Greven, Hartmut; Walker, Yasmin; Zanger, Klaus (2009). "On the structure of teeth in the viperfishChauliodus sloani Bloch & Schneider, 1801 (Stomiidae)". Bulletin of Fish Biology. 1 (1/2): 87–98.
- Glare, P.G.W. (ed.) (1968-1982): Oxford Latin Dictionary (1st ed.). Oxford University Press, Oxford. ISBN 0-19-864224-5
- Haddock, Steven; Moline, Mark; Case, James (2010). "Bioluminescence in the Sea". Annual Review of Marine Science. 2: 443–493. doi:10.1146/annurev-marine-120308-081028. PMID 21141672.
- Nelson, Joseph S. (2006): Fishes of the World (4th ed.). John Wiley & Sons, Inc. ISBN 0-471-25031-7
- Sepkoski, Jack (2002). "A compendium of fossil marine animal genera". Bulletins of American Paleontology. 364: 560. Retrieved 2011-04-21.
- Woodhouse, S.C. (1910): English-Greek Dictionary - A Vocabulary of the Attic Language. George Routledge & Sons Ltd., Broadway House, Ludgate Hill, E.C. Searchable JPEG fulltext
- Velasco-Hogan, Audrey; Deheyn, Dimitri; Koch, Marcus; et al. (2019). "On the Nature of the Transparent Teeth of the Deep-Sea Dragonfish, Aristostomias scintillans". Matter. 11: 235–249. doi:10.1016/j.matt.2019.05.010.