Sphyrna zygaena
Collection Details
Specimens
Photos
There are no photos available for this taxon yet.
Records
Taxonomic Hierarchy
Chondrichthyes (Cartilaginous Fishes)
Carcharhiniformes (Ground Sharks)
Sphyrnidae (Hammerhead Sharks)
Sphyrna
Sphyrna zygaena (Smooth Hammerhead)
Description
This species account was compiled from
Composite (multiple sources) (Carpenter, K.E. (ed.) 2002. The living marine resources of the Western Central Atlantic. FAO Species Identification Guide for Fishery Purposes. FAO, Rome.)
and processed using AI-assisted text extraction.
It may contain errors in spelling, punctuation, or formatting.
When citing, please reference the original source rather than this page.
Learn more about our species accounts.
Synonymy
None / Sphyrna lewini (Griffith and Smith, 1834), Sphyrna
mokarran (Rüppell, 1837).
Characters
Body elongated and later ally compressed. Head hammer-shaped, its anterior con-
tour strongly arched in young but moderately rounded in adults, without a median indentation but with
a deep rounded depression opposite each nostril; lateral expansions of head very prominent, broad
transversely and narrow from front to back; eyes large (their horizontal diameter almost equal to
length of shortest (fifth) gill sl its, their posterior margins about opposite mouth or just anterior to it;
nostrils with strong prenarial grooves; eyes large, their horizontal diameter greater than length of
shortest (fifth) gill sl its; mouth broadly arched, with sm all labial furrows on lower jaw only, corners of mouth
anterior or about opposite to outer corners of head; teeth triangular, deeply notched posteriorly, with smooth
or weakly serrated edges, mostly cuspidate, and with posterior teeth not keeled and molari form. Fifth
gill sl its shorter than the 4 preceding ones, and located posterior to pectoral-fin origins. First dorsal fin
high, moderately falcate, with its origin above or just behind level of pectoral-fin insertions with its free
rear tip not very slender and ending well anterior to the pelvic-fin origins and its inner margin less than
1/3 the length of its base; second dorsal fin sm all, with a very long inner margin almost twice the length
of its anterior margin, a free rear tip ending well anterior to upper precaudal pit, and a nearly straight to
sh allowly concave posterior margin; anal fin falcate, with base slightly longer than second dorsal-fin
base and a deeply notched posterior margin; pectoral fins short, broad, and slightly falcate, with weakly
concave or nearly straight posterior margins; pelvic fins with straight to sh allowly concave posterior
margins. Colour: brownish olive or plain grey above, white or grey-white below; fins nearly plain, dusky, or
blackish-tipped.
Body shape: elongated. A large hammerhead without a notch at the center of the curved headhead (Ref. 58085); but with prominent lateral indentations; prenarial grooves well-developed; snout short, 1/5 to less than a third of head width; mouth broadly arched (Ref. 114967); the first dorsal fin is moderately high, the second dorsal and pelvic fins are low. Colour olive-grey or dark grey above, white below, and the undersides of the pectoral fin tips dusky (Ref. 58085).
Distribution
Essenti ally circumglobal in tem-
perate and tropical seas; in the area, Nova Scotia
to Florida and the Virgin Isl ands; also nor theast-
ern Brazil to Argentina. Not recorded in the Gulf
of Mexico. Possibly more wide-ranging in the
area.
BATOID FISHES
by J. D. Mc Eachran, Texas A & M University, USA
and M. R. de Carvalho, Ameri can Museum of Natural History, New York, USA
508 Batoid Fishes
TECHNICAL TERMS AND MEASUREMENTS
(straight-line distances)
pectoral fin alar spines (or
thorns) of males
pelvic fin, anterior lobe
spiracle
pelvic fin, posterior lobe
thorns of clasper of males 1st dorsal 2nd dorsal
orbit
median row fin fin
caudal fin
lateral tail
axil of fold
inner margin
pectoral
of pelvic fin
fin
upper side of a typical skate (family Rajidae)
length of snout,
preorbital tail spine (sting) dorsal cutaneous fold
length of disc
ventral cutaneous fold
length of
base of tail in stingrays (family Dasyatidae)
snout, preoral
anus
mouth width of
disc
nasal
apertures
length of tail
gill sl its
lower side of typical skate
total 41
rows
snout angle in front of
level of spiracles
anterior part of disc of a skate teeth of a stingray
(arrows indicate method of counting
pavement pattern in batoids)
General Remarks 509
GENERAL REMARKS
Batoid fishes are moderately to greatly flattened and are distinguished from the o ther elamsobranchs
(sharks) by their ventral gill sl its, their lack of an anal fin, and by having the pectoral fins connected to the
sides of the head and trunk to form a disc. The eyes and well-developed spiracles are usu ally located on the
dorsal surface of the head, these are secondarily located on the sides of the head in the more pelagic rays, and
eyes are vestigial in a few electric rays. Sawfishes and guitarfishes are shark-like, in being only moderately flat-
tened and later ally exp anded, with pectoral fins uniting anteriorly to the sides of the head. They possess rela-
tively stout tails that are not clearly demarcated from the disc, and well-developed caudal fins. These forms,
like sharks, swim by later ally undulating their trunk musculature. Electric rays, skates, and stingrays are greatly
flattened and later ally exp anded, with the pectoral fins united anteriorly with the sides of the snout. They pos-
sess a slender tail that is clearly demarcated from the disc, so the head and trunk thus form a circular, ovate, or
rhombic disc. These forms swim by vertic ally undulating or oscillating their discs. The mouth and nostrils are
ventr ally or subtermin ally located in all batoids except they are terminal in Manta. The majority of the batoids
have 2 dorsal fins, but some electric rays, skates, and stingrays have ei ther a single dorsal fin or no dorsal fins.
Jaw teeth are arranged in transverse rows, and like sharks are constantly replaced from inside the mouth;
teeth are later ally fused to form large tooth plates in some of the more pelagic rays. Batoids vary from being
more or less evenly c overed with tooth-like placoid scales or dermal denticles (occasion ally enlarged into
thorns, bucklers, or spines) to completely lacking scales and scale-like structures.
Batoids, like sharks, have cylindrical copulatory organs or claspers derived from pelvic girdle cartilages that
are used for internal fertilization of eggs in females. All batoids, except skates, are viviparous without placen-
tas. Fetuses of sawfishes and guitarfishes are nourished by contents of the yolk sacs but fetuses of stingrays
are furnished with histotroph or uterine milk after they exhaust the contents of their yolk sacs. Skates, on the
o ther h and, are oviparous, and deposit the fertilized eggs in rectangular, horn-like egg capsules that are de-
posited on the bottom.
Batoids vary greatly in size, ranging in total length from about 13 to 20 cm, in some electric rays (Narcinidae)
and skates, to over 7 m in sawfishes; some species may reach a disc width of about 6.1 m (manta rays); and
ranging in weight from 10 to 20 g to between 1 and 3 t. Most batoids are sm all to moderate in size, below 1 m
and 60 cm wide.
Most batoids are generalized benthic predators that lack specialized food capturing and processing struc-
tures. These generalists consume a wide variety of infaunal and epifaunal benthic organisms ranging from
polychaetes and o ther soft-bodied invertebrates to relatively sm all ray-finned fishes. Some electric rays
(Torpedinidae) use their electric organs to stun large fishes that are sw allowed whole; sawfishes use their
rostral saws to disable or kill schooling fishes; and eagle rays and cownose rays use their plate-like teeth to
crush hard-shelled organisms such as oysters and clams. Manta rays have specialized filter plates associated
with their gill arches and feed on zooplankton and nekton. Although primarily marine animals, batoids are also
found in brackish estuaries and lagoons or rivers, but only 1 family of rays, the Potamotrygonidae, is confined
to fresh waters (South Ameri can rivers draining into the Atlantic Ocean). Batoids are widely distri buted in all
oceans, from the Arctic to the Antarctic and from sh allow coastal waters to great depths. Skates have the
greatest latitude and depth ranges, with representatives at most latitudes and depths to about 2 000 m, but are
r are in tropical sh allow waters and coral reef areas. Some electric rays (Torpedinidae) are also abundant in
temperate latitudes; but all remaining batoid families are restricted to tropical and warm-temperate areas, and
show a p
Habitat Associations
Common to abundant coastal and semi-oceanic, living close inshore (espe-
ci ally the young) and near surface in deep water not far offshore. A strong-swimming shark, migrating north-
ward in summer; young often found in large schools of hundreds of individuals. Number of young 29 to 37 per
litter. Feeds on bony fishes, o ther sharks, rays, crustaceans, and squids. Caught with pelagic longlines, h and-
lines, and even pelagic and bottom trawls. Utilized fresh, dried-salted, and possibly smoked; hides are pro-
cessed for lea ther; liver oil is extracted for vitamins; fins are processed into shark-fin soup base; and carcasses
utilized for fish meal. It is uncertain if this
shark figures in shark viewing within the area.
Biology
Maximum total length probably between 3.7 and 4 m, commonly between 2.75 and 3.35 m; size at birth
between 50 and 60 cm; adults maturing at about 210 to 240 cm.
Occurs inshore and well offshore (Ref. 5578), over continental and insular shelves (Ref. 244). Coastal, pelagic, and semi-oceanic, but often bottom associated at 1-139 m (Ref. 58302). Migrates northward in summer; young often in large aggregations of hundreds of individuals (Ref. 13562). Prefers to feed on small sharks, skates and stingrays, but also preys on bony fishes, shrimps, crabs, barnacles and cephalopods (Ref. 244). Viviparous (Ref. 50449). Regarded as being dangerous to people, though only few can be tentatively attributed to this species due to its occurrence in temperate waters (Ref. 244). Reported to cause poisoning (Ref. 4690). Caught occasionally by shark and tuna longline fisheries (Ref.58048). Meat utilized fresh, dried-salted, and possibly smoked for human consumption; liver oil for vitamins, fins for soup, hide for leather, and carcasses for fishmeal (Ref. 244). Used in Chinese medicine (Ref. 12166). Become sexually mature when 250 to 300 cm long. The female gives birth to 30 - 40 young (Ref. 35388).
Reproductive mode: dioecism; fertilization: internal (oviduct); bearers (internal live bearers). Viviparous, placental (Ref. 50449), with 20 to 50 young per litter (Ref. 6871)after a gestation period of 10-11 months (Ref.58048). Size at birth between 50-60 cm TL (Ref. 13562).
IUCN Red List Status: Vulnerable (VU), assessed 2018-11-08. Resilience: Low (tmax=21; tm=8.8; Fec=20-40).
Commercial or Environmental Importance
Conservation status uncer-
tain because of this species being confused with
o ther species, particularly Sphyrna lewini, but of
concern as with that species because of heavy
fisheries where it occurs.
References
Bigelow, H.B. and W.C. Schroeder. 1953. Sawfishes, guitarfishes, skates and rays, and chimaeroids. In Fishes of the Western North Atlantic, Part 2 edited by J. Tee-Van, C.M. Breder, A.E. Parr, W.C. Schroeder, and L.P. Schultz. New Haven: Sears Found. Mar. Res. Mem., 1.
Compagno, L.J.V. 1973. Interrelationships of living elasmobranchs. In Interrelationships of fishes, edited by Greenwood, P.H., R.S. Miles, and C. Patterson. New York, Academic Press, pp. 15-61.
Compagno, L.J.V. 1977. Phyletic relationships of living sharks and rays. Amer. Zool., 17:303-322. McEachran, J.D., K.A. Dunn, and T. Miyake. 1996. Interrelationships of batoid fishes (Chondrichthyes: Batoidae). In Interrelationships of fishes, edited by M.L.J. Stiassny, L.R. Parenti, and G.D. Johnson. New York, Academic Press, pp. 63-84. McEachran, J.D. and K.A. Dunn. 1998. Phylogentic analysis of skates, a morphologically conservative clade of elasmobranches (Cheondrichthyes: Rajidae). Copeia (1998):271-290.
Compagno, L.J.V. (1984) FAO Species Catalogue. Vol. 4. Sharks of the world. An annotated and illustrated catalogue of shark species known to date. Part 2 - Carcharhiniformes. FAO Fish. Synop. 125(4/2):251-655. Rome: FAO.
Compagno, L.J.V., D.A. Ebert and M.J. Smale (1989) Guide to the sharks and rays of southern Africa. New Holland (Publ.) Ltd., London. 158 p.
Smale, M.J. (1991) Occurrence and feeding of three shark species, Carcharinus brachyurus, C. obscurus and Sphyrna zygaena, on the eastern Cape coast of South Africa. S. Afr. J. Mar. Sci. 11:31-42.
Muus, B.J. and J.G. Nielsen (1999) Sea fish. Scandinavian Fishing Year Book, Hedehusene, Denmark. 340 p.
Bowman, R.E., C.E. Stillwell, W.L. Michaels and M.D. Grosslein (2000) Food of northwest Atlantic fishes and two common species of squid. NOAA Tech. Memo. NMFS-NE 155, 138 p.
Compagno, L.J.V., D. Dando and S. Fowler (2005) Sharks of the world. Princeton field guides. Harper Collins Publishing Ltd., London. 368 p.
Ebert, D.A., S. Fowler and M. Dando (2015) A pocket guide to sharks of the world. Princeton University Press, New Jersey,
Comments On Sphyrna zygaena