Cyclothone

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Cyclothone
Cyclothone microdon1.jpg
Veiled anglemouth (C. microdon)
Cyclothone pallida.jpg
Tan bristlemouth (C. pallida)
Scientific classification e
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Stomiiformes
Family: Gonostomatidae
Genus: Cyclothone
Goode & T. H. Bean, 1883

Cyclothone is a genus containing 13 extant species of bioluminescent fish, commonly known as 'bristlemouths' or 'bristlefishes' due to their shared characteristic of sharp, bristle-like teeth. These fishes typically grow to around 1-3 inches (though some can be larger). They are most commonly found in the mesopelagic zone of the ocean, and are mostly found at depths of over 300 meters (1,000 feet).[1]

Cyclothone is believed to be the most abundant genus of fish on Earth, with estimates that there are up to a quadrillion individuals (i.e. one million billion in the short scale or 1015). [2][3] Their abundance is so large that they are also believed to be the most abundant genus of vertebrates on earth.[4]

Distribution and Habitat[]

Cyclothone are found mostly in the open ocean at tropical to temperate latitudes.[5][6] Within the water column, they reside in the mesopelagic zone (also sometimes called the Ocean Twilight Zone). Cyclothone fishes are found in the aphotic zone and have limited access to light (and light dependent food sources). Some species of this genus, such as Cyclothone signata, are believed to migrate towards the surface, although they do not appear to do so in a diel vertical migration pattern. Other species, such as Cyclothone acclinadens, are believed to remain at depth for their entire lives.[7]

Life in the Deep[]

All species in the genus Cyclothone live in the midwater range of the deep sea, and are most commonly found in the mesopelagic zone at 300-1500 meters depth (roughly 1,000- 5,000 feet).[7] The deep sea is an extreme habitat, and life in the deep ocean has specialized adaptations to survive. Light is virtually absent (<1%) in the deep sea, meaning that organisms living there cannot rely on using their eyes to catch prey, avoid predators, or find mates. The deep ocean is also very cold due to the lack of light and sheer volume. Below 200 meters, the average temperature of the ocean is 4°C.[8] Organisms in the deep sea are also subject to immense pressure, with pressure increasing by 1 atmosphere (equivalent to the pressure we feel at on land at sea level) for every 10 meters depth. At 1,000 meters, the pressure of the ocean is equivalent to 100 times that of pressure experienced at sea level.[9]

In order to survive in such extreme conditions, organisms must be highly specialized to match their physiological tolerances to the physical conditions of the deep sea. For example, deep sea organisms do not possess gaseous structures such as lungs or air-pocket swim bladders, as they would burst from the extreme pressure at depth.[9] Specialized adaptations to deep sea conditions have been part of the reason why Cyclothone have been wildly successful in regards to biomass, but also make them difficult to study. Cyclothone fishes cannot survive when brought to the surface, and therefore cannot be observed alive in a laboratory setting. [7][10]

Species[]

Picture of a fish next to a ruler
Image of a preserved Cyclothone, likely Cyclothone acclinidens.

There are currently 13 recognized extant[10] and one extinct[11] species in this genus:

Feeding and Diet[]

In general, Cyclothone fishes appear to be opportunistic feeders and tend to feed on whatever species they can encounter in their extreme environment.[12] Some species have been thought to migrate towards the surface to feed (though not on a Diel Vertical Migration pattern), but some remain at depth their entire lives.[7] They have been commonly known to eat copepods and chaetognaths,[13] but they have also been known to eat euphasiids, mysid shrimp, ostracods, detritus, and even fecal pellets.[12]

Cyclothone falls in the middle of the food web, and its main predators are slightly larger deep-sea fishes, such as dragonfish and fangtooths.[2] One adaptation that could lend a clue to our understanding of predator avoidance strategies in Cyclothone has to do with their bioluminescence. In the midwater region of the deep sea, predators cannot see below, but can sometimes use the small amount of light available to see shadows above them. Cyclothone fishes have small bioluminescent spots to blend in with the surrounding light, allowing them to remain unseen to predators below. This is an adapative strategy in prey known as counter-illumination.[14]

Reproduction[]

Little is known about reproduction in Cyclothone fishes due to the difficulty in observing individuals in situ. Cyclothone are believed to be protandrous, meaning all individuals begin life as males and some become females at reproductive age.[15] Sex determination in reproductive-age Cyclothone is typically dependent on environmental conditions. Males tend to be slightly smaller than females and appear to have a stronger sense of smell. Having a strong sense of smell is likely ecologically advantageous for males in order to find mates in the darkness. [2][16]

Conservation Status[]

At the present time, there are no species of Cyclothone on the ICUN Red List and they have not been thoroughly evaluated by conservation scientists.[6] Because Cyclothone is believed to be the most abundant vertebrate genus on Earth, it is not believed that any of the species are in immediate threat of extinction.[4] However, deep sea ecosystems are fragile and are particularly sensitive to anthropogenic changes, both immediate (such as deep-sea fishing)[17] and long- term (such as climate change).[18]

References[]

  1. ^ Proujan. C., (1979), SECRETS OF THE SEA, 2nd ed., London: Reader's Digest Association Limited pg.60
  2. ^ a b c Broad, William J. (2015-06-29). "An Ocean Mystery in the Trillions". The New York Times. Retrieved 2020-09-28.
  3. ^ "Bristlemouth dominance: How do we know? -Ocean Twilight Zone". WHOI- Ocean Twilight Zone. Retrieved 2020-09-28.
  4. ^ a b Irigoien, Xabier; Klevjer, T. A.; Røstad, A.; Martinez, U.; Boyra, G.; Acuña, J. L.; Bode, A.; Echevarria, F.; Gonzalez-Gordillo, J. I.; Hernandez-Leon, S.; Agusti, S. (2014-02-07). "Large mesopelagic fishes biomass and trophic efficiency in the open ocean". Nature Communications. 5 (1): 3271. Bibcode:2014NatCo...5.3271I. doi:10.1038/ncomms4271. ISSN 2041-1723. PMC 3926006. PMID 24509953.
  5. ^ McKelvie, D (September 1989). "Latitudinal variation in aspects of the biology of Cyclothone braueri and C. microdon (Pisces: Gonostomatidae) in the eastern North Atlantic Ocean". Marine Biology. 102 (3): 413–424. doi:10.1007/BF00428494. S2CID 85367773.
  6. ^ a b "Tan Bristlemouth". Oceana. Retrieved 2020-09-26.
  7. ^ a b c d DeWitt, Floyd A. (1972-03-08). "Bathymetric Distributions of Two Common Deep-Sea Fishes, Cyclothone acclinidens and C. signata, off Southern California". Copeia. 1972 (1): 88–96. doi:10.2307/1442785. JSTOR 1442785.
  8. ^ "What conditions exist for life in the deep ocean? : Ocean Exploration Facts: NOAA Office of Ocean Exploration and Research". oceanexplorer.noaa.gov. Retrieved 2020-09-28.
  9. ^ a b "How does pressure impact animals in the ocean? : Ocean Exploration Facts: NOAA Office of Ocean Exploration and Research". oceanexplorer.noaa.gov. Retrieved 2020-09-28.
  10. ^ a b Froese, Rainer and Pauly, Daniel, eds. (2012). Species of Cyclothone in FishBase. February 2012 version.
  11. ^ a b Nazarkin, M. V. (2015). "Fossil bristlemouth Cyclothone mukhachevae sp. nov. (Stomiiformes: Gonostomatidae) from the Neogene of western Sakhalin, Russia". Paleontological Journal. 49 (2): 162–175. doi:10.1134/S0031030115020045. S2CID 128915597.
  12. ^ a b DeWitt, Floyd A.; Cailliet, Gregor M. (1972-12-29). "Feeding Habits of Two Bristlemouth Fishes, Cyclothone acclinidens and C. signata (Gonostomatidae)". Copeia. 1972 (4): 868. doi:10.2307/1442749. JSTOR 1442749.
  13. ^ Collard, Sneed B. (1970-06-01). "Forage of Some Eastern Pacific Midwater Fishes". Copeia. 1970 (2): 348–354. doi:10.2307/1441657. JSTOR 1441657.
  14. ^ Davis, Matthew P.; Holcroft, Nancy I.; Wiley, Edward O.; Sparks, John S.; Leo Smith, W. (2014-05-01). "Species-specific bioluminescence facilitates speciation in the deep sea". Marine Biology. 161 (5): 1139–1148. doi:10.1007/s00227-014-2406-x. ISSN 1432-1793. PMC 3996283. PMID 24771948.
  15. ^ Miya, Masaki; Nemoto, Takahisa (1987-09-01). "Reproduction, growth and vertical distribution of the meso- and bathypelagic fish Cyclothone atraria (Pisces: Gonostomatidae) in Sagami Bay, Central Japan". Deep Sea Research Part A. Oceanographic Research Papers. 34 (9): 1565–1577. Bibcode:1987DSRA...34.1565M. doi:10.1016/0198-0149(87)90109-9. ISSN 0198-0149.
  16. ^ de Mitcheson, Yvonne Sadovy; Liu, Min (2008-03-01). "Functional hermaphroditism in teleosts". Fish and Fisheries. 9 (1): 1–43. doi:10.1111/j.1467-2979.2007.00266.x. ISSN 1467-2960.
  17. ^ "Our Current Focus". Deep Sea Conservation Coalition. Retrieved 2020-09-26.
  18. ^ Levin, Lisa A.; Le Bris, Nadine (2015-11-13). "The deep ocean under climate change". Science. 350 (6262): 766–768. Bibcode:2015Sci...350..766L. doi:10.1126/science.aad0126. ISSN 0036-8075. PMID 26564845. S2CID 206641418.


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