UrolophidaeRound rays

Di­ver­sity

The fam­ily Urolophi­dae, also known as stin­ga­rees, con­sists of two gen­era and about 35 species. They are bot­tom-dwelling rays in warm seas, usu­ally lying par­tially buried under the sand. Their rounded pec­toral discs are col­ored to blend in with the sand, mud, or rocks on which they live. Urolophids are rel­a­tively small rays, and feed on a va­ri­ety of in­ver­te­brates, small fishes, and crus­taceans. Their tails, dis­tin­guished by the pres­ence of a well-de­vel­oped cau­dal fin, are equipped with one or more ser­rated sting­ing spines. Like other rays they are vi­vip­a­rous; urolophids give birth to be­tween two and four young each year, or in some cases, every two years. Be­cause of their low birth rates and some­times re­stricted range, urolophids are sus­cep­ti­ble to human ac­tiv­ity, al­though only one species is cur­rently known to be threat­ened. (Böhlke and Chap­lin, 1968; Com­pagno, 1999; Ham­lett and Koob, 1999; Last and Stevens, 1994; Moyle and Cech, 2000; Nel­son, 1994; The World Con­ser­va­tion Union, 2002; Wheeler, 1985; Wourms and Dem­ski, 1993)

Ge­o­graphic Range

Urolophids can be found in the east­ern In­dian Ocean, the west­ern Pa­cific, the east­ern Pa­cific from Cal­i­for­nia to Chile, and the west­ern At­lantic, in­clud­ing the Caribbean. They are not known in the west­ern In­dian Ocean, the Mediter­ranean, or the east­ern At­lantic. (Böhlke and Chap­lin, 1968; Last and Stevens, 1994; Nel­son, 1994; Wheeler, 1985)

Habi­tat

Urolophi­dae is a ma­rine fam­ily, al­though some mem­bers enter es­tu­ar­ies. Re­stricted to trop­i­cal and warm tem­per­ate wa­ters, urolophids are bot­tom-dwellers along coast­lines and along the con­ti­nen­tal shelf. Most live in rel­a­tively shal­low water but some oc­cupy depths of at least 700 m down the con­ti­nen­tal slope. They gen­er­ally pre­fer sandy bot­toms in which they can bury them­selves, but a few species live on rocky sub­strates (bot­toms) or in as­so­ci­a­tion with sea veg­e­ta­tion such as kelp. Urolophids tend to have pat­terns and col­or­ing that blend in with their en­vi­ron­ment. (Böhlke and Chap­lin, 1968; Last and Stevens, 1994; Nel­son, 1994; Wheeler, 1985)

Phys­i­cal De­scrip­tion

Urolophids, or stin­ga­rees, are rays with a rounded, oval, or rhom­boidal disc cre­ated by the pec­toral fins. The disc is less than 1.3 times as broad as it is long. Their snouts are con­flu­ent with the rest of the disc. From the side they ap­pear rel­a­tively flat, with the head not el­e­vated. The spir­a­cles (res­pi­ra­tory open­ings) are close be­hind the eyes, which are dor­so­lat­eral (above and to ei­ther side) on the head. The mouth is small and lo­cated on the un­der­side of the snout, and often has sev­eral papil­lae on its floor. Teeth are small and do not form flat crush­ing plates as in some other rays. There are five pairs of small gill open­ings, and the in­ter­nal gill arches do not have fil­ter plates or ridges. Some stin­ga­rees lack a dor­sal fin; in oth­ers the fin is small, lo­cated just in front of the sting and be­hind the pelvic fins. The ser­rated sting­ing spine, lo­cated about halfway down the tail, is large and func­tional. A dis­tin­guish­ing fea­ture of these rays is the pres­ence of a mod­er­ately large, elon­gated cau­dal fin that ex­tends to the tip of the tail. In the genus Urolo­phus the cau­dal fin lobes are con­flu­ent, while in the genus Urotry­gon they are sep­a­rate. The tail is slen­der but not whip-like, and shorter than in stingrays. In col­oration stin­ga­rees range from uni­form gray­ish, yel­low­ish, or brown­ish, to pat­terns of spots, retic­u­la­tions, or dark mask-like bands. Their discs may be smooth or cov­ered with small den­ti­cles. These rays tend to be small, not more than 76 cm in length. (Böhlke and Chap­lin, 1968; Com­pagno, 1999; Last and Stevens, 1994; Nel­son, 1994; Wheeler, 1985)

De­vel­op­ment

Mem­bers of the fam­ily Urolophi­dae, like other rays and their shark rel­a­tives, em­ploy a re­pro­duc­tive strat­egy that in­volves in­vest­ing large amounts of en­ergy into rel­a­tively few young over a life­time. Once sex­u­ally ma­ture, stin­ga­rees have only one lit­ter per year, usu­ally bear­ing two to four young. Since few young are pro­duced, it is im­por­tant that they sur­vive, and to this end rays are born at a large size, able to feed and fend for them­selves much like an adult. Rays de­velop from egg to ju­ve­nile in­side the mother’s uterus, some­times to al­most half their adult size. In this sys­tem, called apla­cen­tal uter­ine vi­vipar­ity, de­vel­op­ing em­bryos re­ceive most of their nu­tri­ment from a milky, or­gan­i­cally rich sub­stance se­creted by the mother’s uter­ine lin­ing. An em­bryo ab­sorbs this sub­stance, called his­totroph, by in­ges­tion, or through its skin or other spe­cial­ized struc­tures. Re­searchers have found that in some rays, the stom­ach and spi­ral in­tes­tine are among the first or­gans to de­velop and func­tion, so that the em­bryo can di­gest the uter­ine “milk.” Rays’ eggs are small and in­suf­fi­cient to sup­port the em­bryos until they are born, al­though the first stage of de­vel­op­ment does hap­pen in­side ter­tiary egg en­velopes that en­close each egg along with egg jelly. The em­bryo even­tu­ally ab­sorbs the yolk sac and stalk and the his­totroph pro­vides it with nu­tri­tion. De­vel­op­ment in the uterus usu­ally takes about three months. (Böhlke and Chap­lin, 1968; Ham­lett and Koob, 1999; Last and Stevens, 1994; Moyle and Cech, 2000; Wheeler, 1985)

Re­pro­duc­tion

Only a few species of elas­mo­branchs have been ob­served dur­ing courtship and mat­ing. How­ever, stin­ga­rees have a sys­tem that in­volves in­ter­nal fer­til­iza­tion, so it can log­i­cally be in­ferred that mat­ing com­mu­ni­ca­tion be­tween male and fe­male must hap­pen to an ex­tent that al­lows the male to in­sert at least one of his two claspers (male re­pro­duc­tive or­gans that are mod­i­fi­ca­tions of the pelvic fins) into the fe­male’s cloaca to de­posit sperm. Elas­mo­branch fishes have rel­a­tively com­plex en­docrine (hor­monal) sys­tems; based on knowl­edge of other ver­te­brates with sim­i­lar sys­tems, it is likely that fe­males sig­nal to males through chem­i­cal or be­hav­ioral cues to in­di­cate when their hor­monal state is ap­pro­pri­ate for mat­ing. In Uro­batis ja­maicen­sis re­searchers found that gland se­cre­tions seal the open groove on males’ claspers into a closed tube that pro­tects semen from being di­luted be­fore it passes into the fe­male. These se­cre­tions co­ag­u­late on con­tact with sea water, help trans­port sperm into the fe­male, and pro­vide lu­bri­ca­tion for clasper in­ser­tion. (Ham­lett and Koob, 1999; Ham­lett, 1999; Wourms and Dem­ski, 1993)

Preg­nancy in at least some urolophids lasts about three months, gen­er­ally span­ning some pe­riod in the spring, sum­mer, and fall. It may take up to two years, how­ever, for the egg fol­li­cle to ac­cu­mu­late enough yolk for ovu­la­tion (re­lease of an egg to be fer­til­ized) as in the case of Uro­batis hal­leri. This means that at least some stin­ga­rees may have lit­ters only once every two years, but it is likely that other groups within the fam­ily give birth on a yearly cycle. Within any given group of rays, in­di­vid­u­als ap­pear to go through mat­ing, ges­ta­tion, and par­tu­ri­tion (birth) at the same time as all the other fe­males in the group. Stin­ga­rees usu­ally bear be­tween two and four young at a time, after nour­ish­ing the em­bryos with milky fluid (his­totroph) se­creted by the uterus (see De­vel­op­ment for a de­scrip­tion of this sys­tem, called apla­cen­tal uter­ine vi­vipar­ity). In some groups the ep­ithe­lium, or wall, of the uterus is mod­i­fied to form tro­phone­mata, elon­gated villi that ex­tend into the uter­ine cav­ity to pro­vide greater sur­face area for res­pi­ra­tory ex­change and his­totroph ex­cre­tion. This ad­vanced sys­tem of nour­ish­ing young in­side the uterus can pro­duce off­spring that are rel­a­tively large at birth (see De­vel­op­ment). Ac­cord­ing to one in­ves­ti­ga­tor, a young ray is rolled up like a cigar dur­ing birth, which, along with the lu­bri­cat­ing his­totroph, fa­cil­i­tates the birth of such pro­por­tion­ally large young. The young ray then un­rolls and swims away. Like­wise, sting-bear­ing young are able to pass out of the mother’s body with­out sting­ing her be­cause their stings are en­cased in a pli­able sheath that sloughs off after birth. (Allen, 1996; Böhlke and Chap­lin, 1968; Ham­lett and Koob, 1999; Helf­man, et al., 1997; Last and Stevens, 1994; Moyle and Cech, 2000; Wheeler, 1985)

No re­ported ev­i­dence of post-birth parental care in Urolophi­dae was found. After such ex­tended nur­tur­ing in­side their moth­ers’ bod­ies, young rays come into the sea quite able to feed and fend for them­selves (see De­vel­op­ment and Re­pro­duc­tion).

Lifes­pan/Longevity

Lit­tle spe­cific in­for­ma­tion re­gard­ing lifes­pans in Urolophi­dae was found, but in gen­eral rays, like their rel­a­tives the sharks, grow and ma­ture slowly and are long-lived. (Last and Stevens, 1994; Moyle and Cech, 2000)

Be­hav­ior

Urolophids (stin­ga­rees) ap­pear to spend most of their time par­tially buried in the sand, or, for a few species, lying on rocks or among sea veg­e­ta­tion. They flap their pec­toral fins to bury them­selves with sand, and also to un­cover the ben­thic (bot­tom-dwelling) or­gan­isms on which they feed. If stepped on they can thrust their flex­i­ble tails up­ward to de­liver a sting with their tail spines. (Böhlke and Chap­lin, 1968; Wheeler, 1985)

Com­mu­ni­ca­tion and Per­cep­tion

Rays per­ceive and in­ter­act with their en­vi­ron­ment using sen­sory chan­nels com­mon to many ver­te­brates: sight, hear­ing, smell, taste and touch. Rays also be­long to a group of fishes, the elas­mo­branchs, whose elec­tri­cal sen­si­tiv­ity seems to ex­ceed that of all other an­i­mals. Elas­mo­branch fishes are equipped with am­pul­lae of Loren­zini, elec­trore­cep­tor or­gans that con­tain re­cep­tor cells and canals lead­ing to pores in the an­i­mal’s skin. Sharks and rays can de­tect the elec­tri­cal pat­terns cre­ated by nerve con­duc­tion, mus­cu­lar con­trac­tion, and even the ionic dif­fer­ence be­tween a body (i.e. of prey) and water. In lab ex­per­i­ments, mem­bers of the fam­ily Urolophi­dae changed their feed­ing lo­ca­tion ac­cord­ing to ar­ti­fi­cially in­duced changes in the elec­tri­cal field around them. Other ex­per­i­ments have demon­strated that car­ti­lagi­nous fishes use elec­trosen­sory in­for­ma­tion not only to lo­cate prey, but also for ori­en­ta­tion and nav­i­ga­tion based on the elec­tri­cal fields cre­ated by the in­ter­ac­tion be­tween water cur­rents and the earth’s mag­netic field. Al­though some rays can pro­duce an elec­tric shock to de­fend them­selves or stun prey, mem­bers of the fam­ily Urolophi­dae can­not. They are able, how­ever, to in­flict a ven­omous sting with their tail spine in de­fense. (Allen, 1996; Bleck­mann and Hof­mann, 1999; Helf­man, et al., 1997)

Food Habits

Many stin­ga­rees feed on fishes, worms, shrimps, and other small or­gan­isms they un­cover when they flap their pec­toral fins along the bot­tom. Some are able to eat hard-shelled mol­lusks and crus­taceans. (Wheeler, 1985)

Pre­da­tion

Ray spines, some of them likely be­long­ing to urolophids, have been found em­bed­ded in the mouths of many sharks. The great ham­mer­head Sphyrna mokar­ran, in par­tic­u­lar, ap­pears to spe­cial­ize in eat­ing stingrays. They use their ham­mer-shaped heads to knock a ray to the bot­tom, and then pin the ray, once again with its head, piv­ot­ing around to bite the ray’s disc until the ray suc­cumbs and can be eaten. In ad­di­tion to their de­fen­sive ven­omous sting, most stin­ga­rees have cryp­tic col­or­ing that blends in with the sandy or rocky bot­tom. Some re­searchers de­scribe stin­ga­rees as al­most im­pos­si­ble to find un­less they move. (Böhlke and Chap­lin, 1968; Helf­man, et al., 1997; Last and Stevens, 1994)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

In their ben­thic (on the bot­tom), warm, usu­ally shal­low-wa­ter habi­tat, stin­ga­rees af­fect the pop­u­la­tions of prey an­i­mals such as in­ver­te­brates and small fishes. They in turn are eaten by larger fish and hu­mans. (Helf­man, et al., 1997; Last and Stevens, 1994; Wheeler, 1985)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Stin­ga­rees are sel­dom used com­mer­cially even though large num­bers are fre­quently caught in nets, but sev­eral species have ed­i­ble flesh. Some are re­ported to be “chewy un­less pre­pared prop­erly.” Na­tive peo­ples in many parts of the fam­ily’s range have used ray spines for spear tips, dag­gers, or whips. (Last and Stevens, 1994)

  • Positive Impacts
  • food

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Stin­ga­rees can cause se­ri­ous wounds with their tail spines. The ser­rated spine tip can be dif­fi­cult to re­move with­out surgery if it breaks off in the wound. Be­cause they tend to oc­cupy shal­low water and are often col­ored to blend in with the bot­tom, they are a haz­ard to waders. Some fish­er­men walk with a “stingray shuf­fle” to make the rays swim away with­out step­ping on them and get­ting stung. (Böhlke and Chap­lin, 1968; Last and Stevens, 1994; Wheeler, 1985)

  • Negative Impacts
  • injures humans

Con­ser­va­tion Sta­tus

One species in the Aus­tralian genus Urolo­phus is listed as near threat­ened. It lives in an area of in­tense fish­ing pres­sure, and fe­males often abort em­bryos when cap­tured. These fac­tors, along with low fe­cun­dity (they bear only two young at a time), mak­ing it vul­ner­a­ble to human ac­tiv­ity. Other urolophids, shar­ing these char­ac­ter­is­tics, may be­come threat­ened in the fu­ture. (The World Con­ser­va­tion Union, 2002)

  • IUCN Red List [Link]
    Not Evaluated

Con­trib­u­tors

Mon­ica Wein­heimer (au­thor), An­i­mal Di­ver­sity Web.

Glossary

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.

World Map

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

acoustic

uses sound to communicate

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.

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.

brackish water

areas with salty water, usually in coastal marshes and estuaries.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

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.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

electric

uses electric signals to communicate

estuarine

an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

food

A substance that provides both nutrients and energy to a living thing.

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.

internal fertilization

fertilization takes place within the female's body

intertidal or littoral

the area of shoreline influenced mainly by the tides, between the highest and lowest reaches of the tide. An aquatic habitat.

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).

magnetic

(as perception channel keyword). This animal has a special ability to detect the Earth's magnetic fields.

molluscivore

eats mollusks, members of Phylum Mollusca

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

piscivore

an animal that mainly eats fish

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

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.

venomous

an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

Allen, T. 1996. Shad­ows in the Sea: The Sharks, Skates, and Rays. New York, NY: Lyons and Bu­ford.

Bleck­mann, H., M. Hof­mann. 1999. Spe­cial Senses. Pp. 300-328 in W Ham­lett, ed. Sharks, Skates, and Rays. Bal­ti­more, MD: The Johns Hop­kins Uni­ver­sity Press.

Böhlke, J., C. Chap­lin. 1968. Fishes of the Ba­hamas and Ad­ja­cent Trop­i­cal Wa­ters. Wyn­newood, PA: Pub­lished for the Acad­emy of Nat­ural Sci­ences of Philadel­phia by Liv­ingston.

Com­pagno, L. 1999. Sys­tem­at­ics and Body Form. Pp. 1-42 in W Ham­lett, ed. Sharks, Skates, and Rays. Bal­ti­more, MD: The Johns Hop­kins Uni­ver­sity Press.

Ham­lett, W. 1999. Male Re­pro­duc­tive Sys­tem. Pp. 444-470 in W Ham­lett, ed. Sharks, Skates, and Rays. Bal­ti­more, MD: The Johns Hop­kins Uni­ver­sity Press.

Ham­lett, W., T. Koob. 1999. Fe­male Re­pro­duc­tive Sys­tem. Pp. 398-443 in W Ham­lett, ed. Sharks, Skates, and Rays. Bal­ti­more, MD: The Johns Hop­kins Uni­ver­sity Press.

Helf­man, G., B. Col­lete, D. Facey. 1997. The Di­ver­sity of Fishes. Malden, MA: Black­well.

Last, P., J. Stevens. 1994. Sharks and Rays of Aus­tralia. Aus­tralia: CSIRO.

Liem, K., A. Sum­mers. 1999. Mus­cu­lar Sys­tem: Gross Anatomy and Func­tional Mor­phol­ogy of Mus­cles. Pp. 93-114 in W Ham­lett, ed. Sharks, Skates, and Rays. Bal­ti­more, MD: The Johns Hop­kins Uni­ver­sity Press.

Moyle, P., J. Cech. 2000. Fishes: An in­tro­duc­tion to ichthy­ol­ogy – fourth edi­tion. Upper Sad­dle River, NJ: Pren­tice-Hall.

Nel­son, J. 1994. Fishes of the World – third edi­tion. New York, NY: John Wiley and Sons.

The World Con­ser­va­tion Union, 2002. "IUCN 2002" (On-line). 2002 IUCN Red List of Threat­ened Species. Ac­cessed De­cem­ber 03, 2003 at http://​www.​redlist.​org/​.

Wheeler, A. 1985. The World En­cy­clo­pe­dia of Fishes. Lon­don: Mac­don­ald.

Wourms, J., L. Dem­ski. 1993. The re­pro­duc­tion and de­vel­op­ment of sharks, skates, rays, and rat­fishes: in­tro­duc­tion, his­tory, overview, and fu­ture prospects. Pp. 7-19 in L Dem­ski, J Wourms, eds. The Re­pro­duc­tion and De­vel­op­ment of Sharks, Skates, Rays, and Rat­fishes. Dor­drecht, The Nether­lands: Kluwer Aca­d­e­mic Pub­lish­ers.