Geographic Range
Southern stingrays are found in the the western Atlantic Ocean from New England to
Brazil, with abundant populations in the Caribbean Sea, Gulf of Mexico, Grand Cayman
Island, British West Indies, Bahamas, coastal Belize, and the southern coast of Florida.
- Biogeographic Regions
- nearctic
- neotropical
- atlantic ocean
Habitat
Southern stingrays are a marine species and are generally found in shallow waters
(about 2 meters deep) of bays filled with sea grass beds and algal fields.
- Habitat Regions
- temperate
- tropical
- saltwater or marine
Physical Description
This species is an elasmobranch (a cartilaginous fish) in the superorder
Batoidea
. Batoid species have a broad, flat, disc-shaped body that is formed by the fusion
of the dorsoventrally flattened body, pectoral fins, and the head. In southern stingrays,
the body and pectoral fins are expanded to form a diamond-shaped disc, which is about
1.2 times as broad as it is long, with females generally being larger than males.
The disc width of Southern stingrays raised in captivity ranges from 48 to 53cm in
males and 75 to 80cm for females. In captivity, the maximum reported disc width for
male is 80cm and for female is 150cm. Wild southern stingrays have reached a maximum
disc width of 200cm and a weight of 97kg. The tail can be up to twice as long as the
body, and carries a sharp, serrated, venomous spine that is used in defense. The gills
are located on the underside of the body. The eyes are located on top of the head,
which is elevated above the rest of the body. Due to its feeding habits and elevated
head, southern stingrays have spiracles that enable them to take in water dorsally.
The skin is covered with denticles, which are scale-like body coverings. Body coloration
ranges between dark gray, green, and brown.
- Other Physical Features
- ectothermic
- heterothermic
- bilateral symmetry
- venomous
- Sexual Dimorphism
- female larger
Development
Fully-developed young are born soon after hatching from their egg capsules, which
occurs inside the mother's body. Hatchlings resemble minature versions of their parents.
- Development - Life Cycle
- indeterminate growth
Reproduction
Very little is known about the mating systems of southern stingrays. However, one
study was able to report observations based on a single female southern stingray mating
with two males. The female was followed by the two males, with one male eventually
biting and holding onto her pectoral fin. This male then positioned himself so that
his pelvic region was curled toward the female’s urogenital opening (also known as
the cloaca). The male then flipped upside down and thrust his pelvic region in a rapid
sequence for 10 to 33 seconds. Following this, the male released his bite from the
female’s pectoral disc. Females are able to mate again soon after giving birth
- Mating System
- polygynandrous (promiscuous)
Age at sexual maturity varies with the geographical region. In captivity, females
were impregnated, and thus considered mature, at about 5 to 6 years. Males, on the
other hand, were considered mature at about 3 to 4 years. Maternal size is positively
correlated with the number of offspring, which can range from 2 to 10. Stingrays that
are raised in captivity bear young biannually, while in wild stingrays, it is usually
once a year. Breeding behavior has been observed in early September in the Grand Cayman
Islands, and in late August at Bimini, Bahamas. Gestation period ranges from 125 to
226 days with a mean of 175 days.
Southern stingrays use both primary and secondary nurseries for the development of
young. The primary nursery is a habitat where a female gives birth to her offspring,
while the secondary nursery is habitat where juveniles reach maturity. Little is known
about the specific locations of these nurseries and migration of the offspring between
the two habitats. In Belize, Glovers Reef is a known primary nursery where adult southern
stingrays only visit seasonally for mating or to give birth. Scientists caught juvenile
southern stingrays during the months of May, November, and December at a depth of
10 to 20 m on nearby rocky reef surfaces, which is believed to be a secondary nursery.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- induced ovulation
- fertilization
- ovoviviparous
Southern stingrays are ovoviviparous (producing young by means of eggs that are hatched
inside the body of the female), meaning that unborn young are protected by the mother
due to developing inside her body. During early development, the embryo uses a yolk
sac for its nutrition. After the yolk sac is absorbed, nutrients are provided by the
mother through the secretion of histotroph ("uterine milk"). No further parental investment
occurs after the young stingrays are born.
- Parental Investment
- female parental care
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
Lifespan/Longevity
Very little is known about the average lifespan of this species. In a single study,
the oldest age recorded for males was 12 years. The oldest recorded female was estimated
to be 13 years old.
Behavior
Southern stingrays are generally solitary, but will form groups for mating purposes,
when resting, or for predator protection. They are generally nocturnal, benthic predators
that excavate their prey by flapping the pectoral fins and jetting water from the
mouth to disturb the substrate and uncover their (usually) buried prey. Southern stingrays
propel themselves through the water using undulatory locomotion, which is provided
by their pectoral fins. This movement method provides a high level of maneuverability,
which is required for foraging and escaping predators. One study suggests that
Dasyatis
species may move with the tide, with high tides providing increased food supply.
- Key Behaviors
- natatorial
- nocturnal
- motile
- solitary
Home Range
Southern stingrays are known to move over large distances and may forage in a very
broad area from day to day. However, quantitative estimates for individual home ranges
(assuming they exist), are currently unavailable.
Communication and Perception
One report speculates that southern stingrays may communicate using pheromones. It
was observed that the birth of offspring attracts males, leading scientists to suspect
that birth produces some kind of olfactory attractant that alerts neighboring males,
perhaps arising from organic molecules produced in the female's cloaca. Since female
southern stingrays are able to mate soon after parturition, these could be considered
to be sexual pheromones. Males occasionally touch females before, and bite them during
mating, which may also serve in some communicative capacity.
Like other elasmobranchs, southern stingrays are equipped with highly developed senses
of smell. They also possess thousands of Ampullae of Lorenzini on their undersides,
particularly concentrated around the head, which allow them to sense electrical field
produced by buried prey. Elasmobranchs also have lateral lines for sensing vibrations
in the water, and a well-develped sense of hearing. The eyes of southern stingrays
are not likely to be useful in sensing prey, being placed on top of the head. However,
they are still rather large and well-developed and are likely used to sense predators
and other disturbances in the water above.
- Other Communication Modes
- pheromones
Food Habits
Southern stingrays feed on multiple organisms throughout the day (more so at night),
so they are considered to be continuous foragers and opportunistic feeders. One study
found the stomach contents of a southern stingray to include prey from 15 families,
in four phyla. Major prey were crustaceans, small fishes, and worms.
- Animal Foods
- fish
- mollusks
- aquatic or marine worms
- aquatic crustaceans
Predation
The main predators of stingrays are humans. Another predator of southern stingrays
are great hammerhead sharks (
Sphyrna mokarra
). The shape of this shark’s head enables it to hold down stingrays while feeding
on them. Stingrays will often bury themselves in the sand to avoid detection by predators,
and will also use their venomous tail spine in self defense.
- Anti-predator Adaptations
- cryptic
Ecosystem Roles
Southern stingrays act as predators of several marine fish and invertebrate species,
as well as serving as prey to larger cartilaginous fish species (particularly hammerhead
sharks). A commensal foraging relationship has been documented between southern stingrays
and double-crested cormorants (
Phalacrocorax auritus
), which are common coastal birds ranging from North Carolina to the Gulf of Mexico.
As stingrays excavate the substrate in search of prey, they often stir up fish. The
birds dive in and swim behind the stingrays to feed on snappers and grunts, though
this is only possible in shallow waters. This stingray foraging habit also attracts
follower organisms, which remain near a host in hopes of finding food. Some observed
follower organisms of stingrays include
Caranx bartholomaei
,
Caranx latus
,
Cephalopholis fulva
,
Halichoeres radiatus
,
Halichoeres dimidiatus
,
Dactylopterus volitans
, and
Lactophrys trigonus
. Bluehead wrasse (
Thalassoma bifasciatum
) serve as mutualistic cleaner organisms for southern stingrays.
- bluehead wrasse ( Thalassoma bifasciatum )
- Phalacrocorax auritus (double-crested cormorants)
- Carangoides bartholomaei (yellow jacks)
- Caranx latus (horse-eye jacks)
- Cephalopholis fulva (coney)
- Halichoeres radiatus (puddingwife wrasse)
- Halichoeres dimidiatus
- Dactylopterus volitans (flying gurnard)
- Lactophrys trigonus (buffalo trunkfish)
- flatworms ( Dendromocotyle octodiscus )
- flatworms ( Lecanicephalum peltatum )
- flatworms ( Phyllobothrium cf. kingae )
- flatworms ( Rhinebothrium magniphallum )
- apicomplexan protists ( Haemogregarina dasyatis )
Economic Importance for Humans: Positive
In developing countries, southern stingrays are an important food resource. Southern
stingrays are also a large tourist attraction in coastal and island locations throughout
their range. A popular tourist site for stingray interaction, “Stingray City Sandbar”,
is located in the Cayman Islands. About 150 southern stingrays are found there yearly.
The stingrays at this location are found during the day and in a very crowded space,
where tourists can hand feed them. The venoms found in association with the spines
of stingrays are currently being researched for possible applications in biomedical
and neurobiological applications.
- Positive Impacts
- food
- ecotourism
- source of medicine or drug
- research and education
Economic Importance for Humans: Negative
Southern stingrays are not known to be aggressive towards humans. Since the they are
often found buried in the sand in shallow waters, it is easy to step on them. When
stepped on, they will use their venomous spine in self-defense.
- Negative Impacts
-
injures humans
- bites or stings
- venomous
Conservation Status
Because southern stingrays are large elasmobranchs with relatively low reproductive
rates and slow growth, they are at risk of overfishing. Currently, this species has
no special conservation status. Populations near the United States appear to be healthy,
but there is little information on the populations in other areas where fishing pressure
is heavier.
Growing tourism also appears to be affecting southern stingray populations. This is
illustrated by the case of “Stingray City Bar”. This species is normally active at
night and is a solitary forager, but at this site it is found during the day (when
tourist activity is high) and in close proximity with conspecifics year-round. The
continuous supply of food keeps the stingrays in this area and causes alterations
to their behavior. Another issue is the hand feeding of these wild animals with foods
such as squid, which are not found in their natural diet. Long term feeding with these
abnormal foods can negatively impact southern stingrays by affecting their health
and mobility.
Additional Links
Contributors
Ivana Pavic (author), Radford University, Joel Hagen (editor), Radford University, Jeremy Wright (editor), University of Michigan-Ann Arbor.
- Nearctic
-
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- Atlantic Ocean
-
the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- temperate
-
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- saltwater or marine
-
mainly lives in oceans, seas, or other bodies of salt water.
- benthic
-
Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.
- reef
-
structure produced by the calcium carbonate skeletons of coral polyps (Class Anthozoa). Coral reefs are found in warm, shallow oceans with low nutrient availability. They form the basis for rich communities of other invertebrates, plants, fish, and protists. The polyps live only on the reef surface. Because they depend on symbiotic photosynthetic algae, zooxanthellae, they cannot live where light does not penetrate.
- coastal
-
the nearshore aquatic habitats near a coast, or shoreline.
- ectothermic
-
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
- heterothermic
-
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
- venomous
-
an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).
- indeterminate growth
-
Animals with indeterminate growth continue to grow throughout their lives.
- polygynandrous
-
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- induced ovulation
-
ovulation is stimulated by the act of copulation (does not occur spontaneously)
- fertilization
-
union of egg and spermatozoan
- internal fertilization
-
fertilization takes place within the female's body
- ovoviviparous
-
reproduction in which eggs develop within the maternal body without additional nourishment from the parent and hatch within the parent or immediately after laying.
- female parental care
-
parental care is carried out by females
- natatorial
-
specialized for swimming
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- solitary
-
lives alone
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- pheromones
-
chemicals released into air or water that are detected by and responded to by other animals of the same species
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- vibrations
-
movements of a hard surface that are produced by animals as signals to others
- chemical
-
uses smells or other chemicals to communicate
- electric
-
uses electric signals to communicate
- cryptic
-
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
- food
-
A substance that provides both nutrients and energy to a living thing.
- ecotourism
-
humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.
- drug
-
a substance used for the diagnosis, cure, mitigation, treatment, or prevention of disease
- venomous
-
an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).
- carnivore
-
an animal that mainly eats meat
- piscivore
-
an animal that mainly eats fish
References
Brooks, D., M. Mayes. 1980. Cestodes in four species of euryhaline stingrays from Colombia. Proceedings of the Helminthological Society of Washington , 47: 22-29.
Cartamil, D., J. Vaudo, C. Lowe, B. Wetherbee, K. Holland. 2003. Diel movement patterns of the Hawaiian stingray, Dasyatis lata : implications for ecological interactions between sympatric elasmobranch species. Marine Biology , 142: 841–847.
Chapman, D., M. Corcoran, G. Harvey, S. Malan, M. Shivji. 2003. Mating behavior of southern stingrays, Dasyatis americana (Dasyatidae). Environmental Biology of Fishes , 68: 241–245.
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 Biology of Sharks and Their Relatives, Second Edition . Boca Raton, FL: CRC Press.
Gilliam, D., K. Sullivan. 1993. Diet and feeding habits of the Southern stingray. Bulletin of Marine Science , 52(3): 1007-1013.
Henningsen, A., R. Leaf. 2010. Observations on the Captive Biology of the Southern Stingray. Transactions of the American Fisheries Society , 139: 783–791.
Henningsen, A. 2000. Notes on Reproduction in the Southern Stingray, Dasyatis americana (Chondrichthyes: Dasyatidae), in a Captive Environment. Copeia , 2000(3): 826-828.
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.
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.
Passarelli, N., A. Piercy. 2006. "Southern Stingray" (On-line). Florida Museum of Natural History. Accessed April 29, 2012 at http://www.flmnh.ufl.edu/fish/Gallery/Descript/SouthernStingray/SouthernStingray.html .
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.
Rosenberger, L. 2001. Pectoral fin locomotion in batoid fishes: undulation versus oscillation. The Journal of Experimental Biology , 204: 379-394.
Saunders, D. 1958. The occurrence of Haemogregarina bigemina Laveran and Mesnil, and H. dasyatis n. sp. in marine fish from Bimini, Bahamas, B.W.I.. Transactions of the American Microscopal Society , 77: 404-412.
Sazima, C., J. Krajewski, R. Bonaldo, I. Sazima. 2007. Nuclear-follower foraging associations of reef fishes and other animals at an oceanic archipelago. Environmental Biology of Fishes , 80: 351-361.
Semeniuk, C., W. Haider, A. Cooper, K. Rothley. 2010. A linked model of animal ecology and human behavior for the management of wildlife tourism. Ecological Modelling , 221: 2699–2713.
Semeniuk, C., K. Rothley. 2008. 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.
Semeniuk, C., B. Speers-Roesch, K. Rothley. 2007. 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: 665–677.
Snelson, F., S. Gruber, F. Murru, T. Schmid. 1990. Southern Stingray, Dasyatis americana : Host for a Symbiotic Cleaner Wrasse. Copeia , 1990 (4): 961-965.
Strong, W., F. Snelson, S. Gruber. 1990. Shorter contributions: ichthyology. Copeia , 1990(3): 836-840.
Yokota, L., R. Lessa. 2006. A nursery area for sharks and rays in Northeastern Brazil. Environmental Biology of Fishes , 75: 349-360.