Southern stingray explained

The southern stingray (Hypanus americanus) is a whiptail stingray found in tropical and subtropical waters of the Western Atlantic Ocean from New Jersey to southern Brazil. It has a flat, diamond-shaped disc, with a mud brown, olive, and grey dorsal surface and white underbelly (ventral surface).[1] The barb on its tail is serrated and covered in a venomous mucus, used for self-defense.

Description

The southern stingray is adapted for life on the sea bed. Its flattened, diamond-shaped body is more angular than other rays.[2] The top of the body varies between olive brown and green in adults, dark grey in juveniles, whilst the underside is white.[3] The wing-like pectoral fins are used to propel the stingray across the ocean bottom, whilst the slender tail possesses a long, serrated and venomous spine at the base, used for defence.[4] These spines are not fatal to humans, but are incredibly painful if stepped on. The eyes are situated on top of the head of the southern stingray, along with small openings called spiracles. The location of the spiracles enables the stingray to take in water whilst lying on the seabed, or when partially buried in sediment. Water enters the spiracles and leaves through the gill openings, bypassing the mouth which is on the underside. Female stingrays can grow to a disc width of 150cm (60inches), while the smaller male stingrays reach a maximum size of 67cm (26inches).[5]

Behavior

Southern stingrays are nocturnal predators, who spray water from their mouths or flap their fins vigorously to disturb the substrate and expose hidden prey. This bottom-dwelling species is often found singly or in pairs, and can reach population densities estimated up to 245/km2 in certain shallow systems thought to be nursery grounds.[6] Hypanus americanus exhibit wave-like locomotion using their pectoral fins. This wave-like motion is important for Hypanus americanus because it allows them to escape predators, forage efficiently, and generally maneuver quickly. Typically, they travel large distances and their foraging area is very expansive. One study provided observations that Hypanus americanus swim along the tide, because of the greater food availability along tides. Hypanus americanus are able to do this because of their high maneuverability and efficient wave-like locomotion. Hypanus americanus either remain solitary or form groups. Groups of Hypanus americanus are usually observed when they mate, for predator protection or even when they are just resting.[7] [8] [9] [10]

Foraging

When scientists revealed the contents of the stomach of one Hypanus americanus, they found evidence of a great variety of ingested prey, including small fishes, worms, crustaceans and bivalves.[11] As mentioned earlier in this article, the Hypanus americanus are smooth and efficient swimmers, allowing them to capture a variety of mobile as well as sessile prey. They are opportunistic feeders and continuous foragers.[12]

Predation

To avoid predators, Hypanus americanus bury themselves in substrate. Venomous spines on the tail are used to repel predators, including humans and great hammerhead sharks.[13] [14]

Roles within their ecosystems

In shallow waters, there is a commensal foraging relationship between Hypanus americanus fish and Nannopterum auritum birds in coastal areas generally like the Gulf of Mexico. When foraging, the Hypanus americanus dig through the substrate in search of food; however, this also helps to expose certain other fish hidden in the substrate after which the Nannopterum auritum will follow behind the Hypanus americanus and eat.[15] [16] [17] [18] [19] [20]

Reproduction

Hypanus americanus are ovoviviparous. Fertilized eggs develop inside the mother's body. The embryos receive nutrients from the yolk sack early in development. After the yolk sac is absorbed, the embryos obtain nutrients from the histotroph (the mother's uterine milk). Females reproduce annually. This species gives live birth after a pregnancy which usually lasts between seven and eight months.[21] Parental care ceases once the young are born. In captivity, gestation lasted 135 to 226 days, after which a litter of two to ten young were born.[22]

There is little knowledge or published evidence about the mating systems of Hypanus americanus. Mating stingrays are rarely encountered in the wild. One study, however, does provide detailed observations of Hypanus americanus mating. This study involves observations of one female mating with two males. The study mentions that the female was chased by the two males, with one of the male's biting (or "catching") the female's fin and releasing her after copulation. Females have the ability to mate again soon after giving birth.[23]

Sexual maturity and nursery type

Geographical location plays a large role in the age of sexual maturity. Observations from studies of breeding behavior (of Hypanus americanus during August at Bimini, Bahamas, and early September in Grand Cayman, Cayman Islands). One study shows that when females were placed in captivity, they were considered mature when they were impregnated (around 5 or 6 years old). In this case, males who were 3 or 4 years old were considered to be mature. There is also a difference in the rate at which the females bear young, depending on whether they are raised in captive natural environments or in natural environments. Females raised in captivity bear offspring twice a year, and females that are raised in the wild bear offspring once a year. In addition, there is a positive correlation between the size of the mother and the number of offspring. There is a difference in nurseries for where the Hypanus americanus offspring are raised: there are primary and secondary nurseries which have a clear distinction. The primary nursery is defined as a habitat where a female Hypanus americanus gives birth to her young. On the other hand, the secondary nursery is a habitat where the juvenile Hypanus americanus are raised to mature adults. Little evidence about locations of and migrations between the primary and secondary nurseries is known. An example of a primary nursery is in Belize, where Hypanus americanus females pay seasonal visits for the purposes of mating and giving birth to offspring. During one study, juvenile Hypanus americanus were caught by scientists at 10 to 20 m depths on rock reef surfaces nearby during the months of May, November and December. This specific location of where these juvenile Hypanus americanus were collected was believed to be a secondary nursery.[22] [24]

Communication

Studies of Hypanus americanus have shown that they communicate through pheromone signaling. Males communicate with females before copulating by touching and biting the females. Also, after the female gives birth, she releases pheromones that are most likely believed to be produced in her cloaca; one study reported that the birth of offspring attracted males. As previously mentioned in the article, since a female has the ability to mate soon after giving birth, it is plausible that these are sex pheromones. The role of pheromones in communication also make sense since Hypanus americanus have strong senses of smell. They have many Ampullae of Lorenzini, usually heavily concentrated around the head. In addition, this gives them the ability to sense certain electric fields which are emitted from hidden prey. In addition, they have special mechanisms for senses vibrations in the water as well as for hearing.[25]

Human interaction

In many parts of the Caribbean such as Grand Cayman, Cayman Islands and Antigua, the southern stingray swims with divers and snorkelers, and are hand fed at locations such as Stingray City and the Sandbar.[26] On Turks & Caicos, they can be hand fed at a location called Gibbs Cay. Some have become tame enough to be cradled in visitors' arms and feed with pieces of cut up fish. This docile and food-reward driven behaviour has led to many locals comparing the hand-fed and belly-rubbed stingray to an over-fed household canine. There are concerns that this feeding, and the high levels of interaction with humans, may be having some negative impacts on their behaviour and ecology.[27]

The southern stingray may make its way into the aquarium trade. Despite its relative hardiness, it is best avoided as it requires an immense 4,200 gallon capacity system and will devour any fish or invertebrate it is able to capture.[28] They are also housed within public aquariums and animal theme parks including Six Flags Discovery Kingdom in Vallejo, California and the Long Island Aquarium in Riverhead, New York where visitors are allowed to pet the rays in a touch pool.[29] [30] In public aquariums, female southern stingrays have been seen biting one another on the edges of their fins. Reproduction has also been known to occur within large public aquariums.

External links

Notes and References

  1. Bigelow, H. and Sschroder, W. (1953) Fishes of the Western North Atlantic. Sawfishes, guitarfishes, skates and rays. Mem. Sears Found. Mar. Res. 1, 1-558.
  2. http://www.flmnh.ufl.edu/fish/Gallery/Descript/SouthernStingray/SouthernStingray.html Southern Stingray
  3. Lieske, E. and Myers, R. (2002) Coral Reef Fishes: Indo-Pacific and Caribbean. HarperCollins Publishers, London – via ARKive
  4. Carpenter, K.E. (2001) The Living Marine Resources of the Western Central Atlantic, Volume 1. Food and Agriculture Organization of the United Nations, Rome – via ARKive
  5. McEachran, J. & de Carvalho, M. (2002) "Dasyatidae". In: K.E. Carpenter (ed.). The living marine resources of the Western Central Atlantic. Volume 1. Introduction, molluscs, crustaceans, hagfishes, sharks, batoid fishes and chimaeras. pp. 562–571.
  6. 10.1002/aqc.2317. Population density estimation of southern stingrays Dasyatis americanaon a Caribbean atoll using distance sampling. Aquatic Conservation: Marine and Freshwater Ecosystems. 23. 2. 202. 2013. Tilley. Alexander. Strindberg. Samantha. 2013ACMFE..23..202T .
  7. 10.1007/s00267-006-0321-8. 17638047. Using Fatty-Acid Profile Analysis as an Ecologic Indicator in the Management of Tourist Impacts on Marine Wildlife: A Case of Stingray-Feeding in the Caribbean. Environmental Management. 40. 4. 665–77. 2007. Semeniuk. Christina A. D.. Speers-Roesch. Ben. Rothley. Kristina D.. 2007EnMan..40..665S. 24623615.
  8. Diel movement patterns of the Hawaiian stingray, Dasyatis lata: implications for ecological interactions between sympatric elasmobranch species. Marine Biology. 142. 5. 841. 10.1007/s00227-003-1014-y. 2003. Cartamil. D. P.. Vaudo. J. J.. Lowe. C. G.. Wetherbee. B. M.. Holland. K. N.. 2003MarBi.142..841C . 12785003.
  9. Rosenberger, L.. Pectoral fin locomotion in batoid fishes: Undulation versus oscillation. The Journal of Experimental Biology. 204. Pt 2. 379–94. 11136623. 2001. 10.1242/jeb.204.2.379. 2016-11-11. 2017-01-08. https://web.archive.org/web/20170108173559/http://foodweb.uhh.hawaii.edu/MARE%20594/Rosenberger%202001.pdf. dead.
  10. 10.1016/j.ecolmodel.2010.07.018. A linked model of animal ecology and human behavior for the management of wildlife tourism. Ecological Modelling. 221. 22. 2699. 2010. Semeniuk. Christina A.D.. Haider. Wolfgang. Cooper. Andrew. Rothley. Kristina D.. 2010EcMod.221.2699S .
  11. Web site: Dasyatis americana (Southern Stingray). The Online Guide to the Animals of Trinidad and Tobago . .
  12. Gilliam, D.. Sullivan, K.. amp . 1993. Diet and feeding habits of the Southern stingray. Bulletin of Marine Science. 52. 3. 1007–1013.
  13. Passarelli, N., A. Piercy. (2006). "Southern Stingray". Florida Museum of Natural History. Accessed April 29, 2012
  14. Pikitch, E.. D. Chapman. E. Babcock. M. Shivji. 2005. Habitat use and demographic population structure of elasmobranchs at a Caribbean atoll (Glover's Reef, Belize). Marine Ecology Progress Series. 302. 187–197. 10.3354/meps302187. 2005MEPS..302..187P. free.
  15. Snelson, F.. S. Gruber. F. Murru. T. Schmid. 1990. Southern Stingray, Dasyatis americana: Host for a Symbiotic Cleaner Wrasse. Copeia. 1990 . 4. 961–965. 1446479. 10.2307/1446479.
  16. Sazima, C.. J. Krajewski. R. Bonaldo. I. Sazima. 2007. Nuclear-follower foraging associations of reef fishes and other animals at an oceanic archipelago. 10.1007/s10641-006-9123-3. Environmental Biology of Fishes. 80. 4. 351–361. 2007EnvBF..80..351S . 25188593.
  17. Saunders, D. . 1958. The occurrence of Haemogregarina bigemina Laveran and Mesnil, and H. dasyatis n. sp. in marine fish from Bimini, Bahamas. 3223863. Transactions of the American Microscopical Society. 77. 4. 404–412. 10.2307/3223863.
  18. Kohn, A.. S. Cohen. G. Salgado-Maldonado. 2006. Checklist of Monogenea parasites of freshwater and marine fishes, amphibians and reptiles from Mexico, Central America and Caribbean. Zootaxa. 1289. 1–114. 10.11646/zootaxa.1289.1.1 .
  19. Kajiura, S.. L. Macesic. T. Meredith. K. Cocks. L. Dirk. 2009. Commensal Foraging Between Double-crested Cormorants and a Southern Stingray. The Wilson Journal of Ornithology. 121. 3. 646–648. 10.1676/08-122.1. 44216892.
  20. Brooks, D.. Mayes, M.. amp . 1980. Cestodes in four species of euryhaline stingrays from Colombia. Proceedings of the Helminthological Society of Washington. 47. 22–29.
  21. Ramirez Mosqueda, E., Perez Jimenez, J. C., & Mendoza Carranza, M. (2012). Reproductive parameters of the southern Stingray Dasyatis americana in southern Gulf of mexico. Latin American Journal of Aquatic Research, 40(2), 335–344. https://doi.org/10.3856/vol40-issue2-fulltext-8
  22. Henningsen, A.D. . Notes on reproduction in the southern stingray, Dasyatis americana (Chondrichthyes: Dasyatidae), in a captive environment. Copeia. 3. 826–828. 10.1643/0045-8511(2000)000[0826:NORITS]2.0.CO;2. 1448353. 2000. 2000. 85808594 .
  23. Mating behavior of southern stingrays, Dasyatis americana (Dasyatidae). Environmental Biology of Fishes. 68. 3. 241. 10.1023/A:1027332113894. 2003. Chapman. Demian D.. Corcoran. Mark J.. Harvey. Guy M.. Malan. Sonita. Shivji. Mahmood S.. 2003EnvBF..68..241C . 35083420.
  24. Observations on the Captive Biology of the Southern Stingray. Transactions of the American Fisheries Society. 139. 3. 783. 10.1577/T09-124.1. 2010. Henningsen. Alan D.. Leaf. Robert T.. 2010TrAFS.139..783H .
  25. Gardiner, J., R. Hueter, K. Maruska, J. Sisneros, B. Casper, D. Mann, L. Dernski. (2012). "Sensory Physiology and Behavior of Elasmobranchs", pp. 349-401 in J Carrier, J Musick, M Heithaus, eds. Biology of Sharks and Their Relatives, Second Edition. Boca Raton, FL: CRC Press.
  26. Costs of group-living for a normally solitary forager: effects of provisioning tourism on southern stingrays Dasyatis americana. Marine Ecology Progress Series. 357. 271–282. 10.3354/meps07299. 2008. Semeniuk. CAD. Rothley. KD. 2008MEPS..357..271S. free.
  27. Web site: Stingray Conservation and Ecology Research. cnso.nova.edu. Nova Southeastern University. March 28, 2017.
  28. Book: Michael, Scott . Aquarium Sharks & Rays . T.F.H Publications, Inc. . 2001 . Neptune City, NJ.
  29. Southern Stingray | Six Flags Discovery Kingdom https://www.sixflags.com/discoverykingdom/animalcare/southern-stingray. In: Six Flags Discovery Kingdom https://www.sixflags.com/discoverykingdom

  30. Ray Bay: Interactive Touch Tank - Long Island Aquarium https://www.longislandaquarium.com/ray-bay-2/. In: Long Island Aquarium | Aquatic Adventures https://www.longislandaquarium.com