Pelagic Thresher

Description

The head is narrow with a short, conical snout and a distinctive "pinched" profile when viewed from below. The eyes are very large in juveniles and decrease in relative size with age. No furrows occur at the corners of the mouth. The teeth are very small, numbering 21–22 rows on each side with a symphysial (central) row in the upper jaw and 21 on each side without a symphysial row in the lower jaw. Five to 11 rows of posterior teeth are present. The teeth are smooth-edged, with oblique cusps and lateral cusplets on the outside margins. The body is covered with very small, smooth dermal denticles with flat crowns and cusps with parallel ridges. The coloration is an intense dark blue above and white below; the white does not extend to above the pectoral fins. The color rapidly fades to gray after death. The dark pigment above the pectoral fins, the rounded pectoral fin tips, and the absence of labial furrows separate this shark from the common thresher.

Distribution and habitat

Due to confusion with the common thresher, the distribution of the pelagic thresher may be wider than is currently known. It ranges extensively in the Indo-Pacific, with scattered records from South Africa, the Red Sea and the Arabian Sea (off Somalia, between Oman and India, and off Pakistan), to China, southeastern Japan, northwestern Australia, New Caledonia, and Tahiti, to the Hawaiian Islands, the Gulf of California, and the Galapagos Islands. The North Pacific population shifts northward during warm El Nino years. Analysis of mitochondrial DNA has shown extensive gene flow within the eastern and western Pacific pelagic thresher populations, but little flow between them.

The pelagic thresher primarily inhabits the open ocean, occurring from the surface to a depth of at least 150 m (492 ft). However, it occasionally comes close to shore in regions with a narrow continental shelf, and has been observed near coral reef dropoffs or seamounts in the Red Sea and the Gulf of California, and off Indonesia and Micronesia. It has also been known to enter large lagoons in the Tuamotu Islands.

Biology and ecology

The pelagic thresher is an active, strong swimmer and has been known to leap clear of the water (five times in a row on one documented occasion).Predators of the pelagic thresher include larger fishes (including other sharks) and toothed whales. Known parasites of this species include the tapeworms Litobothrium amplifica, L. daileyi, and L. nickoli, which inhabit the shark's spiral valve intestine, and copepods of the genus Echthrogaleus, which infest the skin. At Malapascua Island in the Philippines, pelagic threshers have been observed regularly visiting cleaning stations occupied by cleaner wrasses (Labroides dimidiatus and Thalassoma lunare), during which they exhibit characteristic behaviors to facilitate the cleaning interaction. These visits occur more frequently early in the morning, and may be why these normally oceanic sharks are sometimes encountered in shallow water.

Feeding

Little information is available on the feeding ecology of the pelagic thresher. Its very slender tail and fine dentition suggest an exclusive diet of small, pelagic prey. Analysis of stomach contents reveal that pelagic threshers feed mainly on barracudinas, lightfishes, and escolars, all inhabitants of the mesopelagic zone. Therefore, little competition occurs between the pelagic thresher and other large oceanic piscivores such as billfishes, tunas, and dolphinfishes, which tend to feed near the surface. As in other threshers, pelagic threshers may swim in circles to drive schooling prey into a compact mass, before striking them sharply with the upper lobe of their tails to stun them. Because of this behavior, pelagic threshers are often hooked on longlines by their tails.

Life history

Like the rest of the mackerel sharks, the pelagic thresher is ovoviviparous. It gives birth to two pups at a time (rarely just one), one per uterus. With no defined breeding season, most adult females are pregnant throughout the year; the gestation period is uncertain, but has been suggested to be less than one year as in the common thresher. The developing embryos are sustained by a yolk sac until they are 12 cm (4.7 in) long, after which they are oophagous and feed on egg capsules produced by the mother. Each capsule measures about 55 mm (2.2 in) long and 12 mm (0.5 in) across, and contains 20–30 ova. Early stage embryos have specialized teeth for opening the capsules, while later-stage embryos have their teeth hidden and swallow the capsules whole, their teeth not becoming functional again until just after birth. No evidence of sibling cannibalism has been found as in the sand tiger shark (Carcharias taurus). Young pelagic threshers are born unusually large, up to 1.6 m (5.2 ft) long or 43% the length of the mother, which likely reduces predation on the newborns.

The growth rate of pelagic threshers slows with age: 9 cm/year for ages 0–1, 8 cm/year for ages 2–3, 6 cm/year for ages 5–6, 4 cm/year for ages 7–10, 3 cm/year for ages 10–12, and 2 cm/year for ages 13 and greater. Females reach maturity at 2.8–2.9 m (9.2–9.5 ft) long and eight to nine years old, while males mature at 2.7–2.8 m (8.9–9.2 ft) long and seven to eight years old. The oldest confirmed ages for females and males are 16 and 14 years respectively. Extrapolating the growth curves to the largest known individuals suggests that females may have a lifespan exceeding 28 years, and males 17 years. A single female produces about 40 young over her entire life.

Thermoregulation

Anatomical examination indicates that the pelagic thresher is unlikely to be warm-bodied like the common thresher. The pelagic thresher lacks a rete mirabile, a blood vessel countercurrent exchange system that prevents metabolic heat from being dissipated into the water, inside its trunk. Furthermore, its aerobic red muscles, responsible for generating heat in the common thresher, are positioned in two lateral strips just beneath the skin rather than at the core of the body. A rete system is present around the pelagic thresher's brain and eyes, albeit less developed than in the bigeye thresher, which may serve to buffer those organs against temperature changes.

Human interactions

The pelagic thresher has never been implicated in an attack on humans; it has small jaws and teeth for its size and tends to flee from divers. This shark is taken by commercial fisheries in the central Pacific and western Indian Oceans, as well as off California and Mexico. Abundant off northeastern Taiwan, it comprises over 12% (about 3,100 fish, 220 metric tons) of the annual Taiwanese shark landings. The meat is sold for human consumption, the skin is made into leather, and the fins are used for shark fin soup in Asia. The squalene oil in the liver of the pelagic thresher can comprise 10% of its weight, and is used in the manufacture of cosmetics, health foods, and high-grade machine oil.

Though rarely caught, pelagic threshers are also valued by sport fishers and are listed as game fish by the International Game Fish Association. The largest overall records are from New Zealand, while the light tackle records are from California. Pelagic threshers are frequently taken as bycatch on longlines and in driftnets meant for other species such as tuna, and also rarely in gillnets and antishark nets. All three thresher shark species were assessed as Vulnerable by the IUCN in 2007, as their low fecundity cannot sustain high levels of exploitation.

Taxonomy and phylogeny

The pelagic thresher was originally described by Japanese ichthyologist Hiroshi Nakamura on the basis of three large specimens, none of which was designated a type specimen. He illustrated one of the three specimens in his paper, "On the two species of the thresher shark from Formosan waters", published in August 1935. Nakamura also separately illustrated and described a fetus, that Leonard Compagno later concluded was probably of a common thresher. Several authors, including Gohar and Mazhar (1964, Red Sea), Kato, Springer and Wagner (1967, Eastern Pacific), Fourmanoir and Laboute (1976, New Caledonia), Johnson (1978, Tahiti), and Faughnan (1980, Hawaiian Islands) have published illustrations of "common threshers" that were in fact pelagic threshers.

An allozyme analysis conducted by Blaise Eitner in 1995 showed that the closest relative of the pelagic thresher is the bigeye thresher (A. superciliosus), with which it forms a clade. The specific epithet pelagicus is from the Greek pelagios, meaning "of the sea". Another common name is the smalltooth thresher