|Range of the chain catshark|
Scyllium retiferum Garman, 1881
The chain catshark or chain dogfish (Scyliorhinus retifer) is a small, reticulated catshark that is biofluorescent. The species is common in the West Atlantic and Gulf of Mexico from George's Bank in Massachusetts, to Nicaragua. It is harmless and rarely encountered by humans. It has very similar reproductive traits to the small-spotted catshark (S. canicula).
The chain catshark is one of four elasmobranch species shown to possesses biofluorescent properties. The researchers of the study examined the vision of Scyliorhinus retifer using microspectrophotometry and designed a "shark-eye" camera that yielded contrast information on areas where fluorescence is anatomically distributed on the shark. The repeated evolution of biofluorescence in elasmobranchs, coupled with a visual adaptation to detect it; and evidence that biofluorescence creates greater luminosity contrast with the surrounding background, highlights the potential importance of biofluorescence in elasmobranch behavior and biology.
Distribution and size
In the Mid-Atlantic Bight, the chain dogfish is found along the outer continental shelf and upper slope. The shark occupies depths of 58 to 359 meters (190 to 1,178 ft) and occupies shallower depths in the northern region compared to southern areas. Due to the shark’s depth distribution, it has been suggested that the shark does not perform large-scale migrations.
Temperature is thought to limit the shark’s distribution in northern areas, particularly during the winter. Although bands of warm water at the edge of the shelf have been observed, the temperature varies seasonally, thus limiting this non-migratory species.
Sizes of the species range from 0.36 feet (0.11 m) (immature), to 1.5 feet (0.46 m) (adult). Females tend to be larger at maturity, being 1.7 feet (0.52 m) long compared to their male counterparts at 1.64 feet (0.50 m).
Habitat and behavior
The catshark spends the daytime resting at the bottom, usually in contact with certain structures. It has been observed with large burrowing cerianthid anemone tubes and boulders. The bottom rubble is thought to be used as a camouflage with the shark’s spotted surface. Adult sharks tend to prefer rough bottoms, creating a difficulty for trawl sampling, while the immature forms are found near smoother regions. The chain catshark has been known to feed on squid, bony fish, polychaetes and crustaceans. In aquaria, they are relatively motionless, only swimming occasionally.
In the female chain catshark, follicle development has been correlated to nidamental gland size, thus, they are considered mature when they have a fully developed nidamental gland or shell gland. This is marked by the glands growth to 18 mm or more in width. Sexual maturity in the female is seen at 520 mm in length under normal conditions. There has been evidence however that some northern populations of the shark may mature at a smaller size (410 mm).
In the male catshark, testis development is correlated to clasper size, thus maturity is marked when it develops hardened claspers that are 30 mm or more in length. Claspers have been observed to develop after the shark is 490 mm and become mature at 500 mm.
Observed mating between the species suggests biting plays an element and that mating occurs repeatedly. Behavioral observations include the male biting the female until it can get a firm grasp and subsequently wraps its body around the female for copulation. After copulation, the male releases his bite and both separate.
The chain catshark prefers vertical structures for egg deposition and always deposits eggs in pairs. The interval between pairs of eggs ranges from a few minutes to 8 days. Development rates average 1mm diameter per 7.7 days although temperature has also been seen to affect follicle development.
Sperm storage and egg cases
The female chain catshark is able to store sperm and lay eggs several days after initial copulation. The shark has been known to store sperm up to 843 days although, there are some circumstances of poor egg development in eggs laid later. It is suggested that this could be due to a number of factors including, senescence, low sperm viability, or water quality factors.
Egg cases found in the oviduct are soft, pale yellow and translucent. They also feature two coiled tendrils, a key adaptation which allows snagging on rocks or man made structures, providing grounding and safety. When deposited, they become hardened and become dark amber with white bands.
10 mm – it has well-defined gill arches and has a thin ventral finfold. 21 mm – dorsal and pelvic fin buds appear 33 mm – embryo has protruding eyes and well-developed gill filaments. 43 mm – it has lost its translucency and develops slits in the egg case, allowing fluid exchange from surrounding seawater and the interior 58 mm – the finfold starts to decay 66 mm – the finfold and gill filaments are reduced or absent 74 mm – external appearance is complete but yolk sac is still being absorbed 100–110 mm – hatching
The chain catshark has been described as "gorgeous," and "an ideal candidate" for being bred in captivity.
- Sherrill-Mix, S.A., Myers, R.A. & Burgess, G.H. (2006). Scyliorhinus retifer. The IUCN Red List of Threatened Species doi:10.2305/IUCN.UK.2006.RLTS.T60233A12331224.en
- Able, Kenneth W.; Flescher, Donald (1991). "Distribution and Habitat of Chain Dogfish, Scyliorhinus retifer, in the Mid-Atlantic Bight". Copea. 1: 231–234. JSTOR 1446270. doi:10.2307/1446270.
- Chain Catsharks, Scyliorhinus retifer. marinebio.org
- Castro, Jose I., Bubucis, Patricia M., and Overstrom, Neal A. (1988). "The Reproductive Biology of the Chain Dogfish, Scyliorhinus retifer". Copea. 3: 740–746. JSTOR 1445396.
- Gruber, David F.; Loew, Ellis R.; Deheyn, Dimitri D.; Akkaynak, Derya; Gaffney, Jean P.; Smith, W. Leo; Davis, Matthew P.; Stern, Jennifer H.; Pieribone, Vincent A.; Sparks, John S. (2016). "Biofluorescence in Catsharks (Scyliorhinidae): Fundamental Description and Relevance for Elasmobranch Visual Ecology". Scientific Reports. 6: 24751. PMC . PMID 27109385. doi:10.1038/srep24751.
- "EXCLUSIVE: How "Glowing" Sharks See Each Other". video.nationalgeographic.com. Retrieved 2016-05-11.
- Sminkey, Thomas R.; Tabit, Christopher R. (1992). "Reproductive biology of the Chain Dogfish, Scyliorhinus retifer, from the Mid-Atlantic Bight". Copea. 1: 251–253. JSTOR 1446564. doi:10.2307/1446564.
- Chain Dogfish. flmnh.ufl.edu
- Michael, Scott W. (March 2004), "Sharks at Home", Aquarium Fish Magazine, pp. 20–29
|Wikimedia Commons has media related to Scyliorhinus retifer.|
- Sherrill-Mix; et al. (2005). "Scyliorhinus retifer". IUCN Red List of Threatened Species. Version 2006. International Union for Conservation of Nature. Retrieved 12 May 2006. Database entry includes justification for why this species is of least concern
- "Scyliorhinus retifer". Integrated Taxonomic Information System. Retrieved 30 January 2006.
- Froese, Rainer and Pauly, Daniel, eds. (2005). "Scyliorhinus retifer" in FishBase. Nov 2005 version.