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BULLETIN OF MARINE SCIENCE, 78(2): 397–402, 2006

NOTE ATTACKS ON A SHARK (RHINCODON TYPUS) AT NINGALOO REEF, WESTERN

Ben Fitzpatrick, Mark Meekan, and Allison Richards

The planktivorous , reputed to attain lengths of up to 18 m, is the world’s largest (Coleman, 1997). The immense size of whale may offer a refuge from (Peters, 1983) by large sharks and killer , Orcinus orca (Linnaeus, 1758), similar to other marine such as cetaceans (Pitman et al., 2001). At present, there is only one published observation that suggests that whale sharks might be susceptible to any top predator other than man (Fertle et al., 1996). However, very little is known of the biology and ecology of these , and the lack of predation records on whale sharks may simply reflect the fact that they usually inhabit tropical oceanic , far from coastal regions where predation is likely to be observed. Ningaloo Reef in hosts an aggregation of whale sharks in coast- al waters from March to June. The predictable arrival of whale sharks has led to the development of a lucrative ecotourism industry that allows divers to observe sharks in shallow waters on the seaward edges of the fringing coral reef. During these whale shark encounters, attacks by a predator, possibly a shark, Galeocerdo cuvier (Péron and Lesueur in Lesueur, 1822), or great , (Linnaeus, 1758), and ectoparasitic sharks ( spp.) were documented. Encoun- ters with the same whale shark 3 mo and then 1 yr later recorded wound healing. This time series provides insight into the predation risk faced by whale sharks despite their size and their ability to recover from attacks that cause substantial wounds. The photographs shown here were taken by snorkelers from ecotourism boats at Ningaloo Reef during 2003 and 2004. A 5.5 m male shark was initially photographed in April 2003 (Figs. 1, 2). The length of the shark was estimated visually by tour operators using the known lengths of snorkelers in the beside the shark. At this time, the shark displayed wounds from at least three attacks. There was a deep wound to the left flank that had partially healed and within this wound were numer- ous oval shaped scars where plugs of flesh had been removed. These oval marks were consistent with bites from the ectoparasitic cookie cutter shark (Isistius spp.) (Jones, 1971). A large shark had also removed most of the dorsal (Figs. 1, 2). Unlike the healed perimeter of the flank wound, there was torn and severed skin, connective tissue, and muscle at the edge of the wound, suggesting that it was very recent. A relatively minor wound was also evident on the right flank of the shark with teeth marks from two bites also clearly from those of a large shark in a similar position to the wound on the left flank (Fig. 2). What appeared to be a protrudes from one of the bite incisions on the right flank below the midline and in line with the center of the dorsal fin (Fig. 2). The clean and sharp edges of these bites suggest that this wound occurred recently, probably at the same time as the removal of the dorsal fin. Despite these wounds, the shark appeared to react normally to swimmers and there was no indication of behavior that might have attracted the attention of predators.

Bulletin of Marine Science 397 © 2006 Rosenstiel School of Marine and Atmospheric Science of the University of Miami 398 BULLETIN OF MARINE SCIENCE, VOL. 78, NO. 2, 2006

Figure 1. Photograph taken in April 2003 of wounds to a 5.5 m female whale shark at Ningaloo Reef. Note numerous scars from cookie cutter sharks in healing wound on left flank. Photo credit: anonymous.

A photograph taken in July 2003 shows the wounds on the left side of the whale shark and the remains of the dorsal fin 3 mo after the first encounter (Fig. 3). The left flank wound had partially healed, although a circular scar in the center suggests that the was still undergoing attacks from cookie cutter sharks. Healing of the wound to the dorsal fin had also progressed and the edges were no longer ragged. A photo taken 1 yr later in June 2004 shows that these wounds had almost completely healed (Fig. 4). Potential culprits for the large wounds on this whale shark are the , , or possibly large individuals of the shark Carcharinus. All of these predators occur at Ningaloo Reef (Last and Stevens, 1994; B.F., unpubl. data) and are known to feed on large cetaceans (Compagno, 1984; Long, 1991; Silber and Brown, 1991) and sharks (Fertl et al., 1996; Fergusson et al., 2000). Furthermore, flesh has been found in the stomachs of white sharks (Springer and Gold, 1989). Killer whales have been reported to attack prey as large as basking sharks in the temperate waters of New Zealand and southern and have been observed attacking a whale shark in the Gulf of California (Fertl et al., 1996). However, based on the shape of the bite and teeth marks on the whale shark, killer whales can be excluded as the predator in this case. The shape and position of the wounds to the whale shark suggest that either a tiger shark or great white may have been responsible for the bites on the dorsal fin and right flank. On average, the dorsal fin height of a 5.5 m whale shark is approximately 42 cm (Press et al., Charles Darwin University, unpubl. data). To inflict a bite of the size shown in Figures 1 and 2, a tiger shark would have to be at least 3.5 m total length NOTES 399

Figure 2. April 2003 photograph of the right flank of the same whale shark as in Figure 1. Note the lines of teeth marks above and below the midline of the shark. Photo credit: anonymous.

(TL) based on the relationship between bite width and TL for this (Heithaus, 2001a). Up to 17% of tiger sharks caught on drumlines set in Shark Bay to the south of Ningaloo Reef were of this size (Heithaus, 2001b). By comparison, published rela- tionships between bite width and TL for white sharks (Bass et al., 1973) show that a bite of this size could have been produced by a white shark of 4 m TL.

Figure 3. July 2003 photograph of the left side of the whale shark. Note healing to wounds and presence of bite scar of cookie cutter shark in center of wound near tail. Photo credit: S. Gibson. 400 BULLETIN OF MARINE SCIENCE, VOL. 78, NO. 2, 2006

Figure 4. June 2004 photograph of the left side of the whale shark. Photo credit: A.R.

Due to healing, it is impossible to determine the likely culprit for the large wound on the left hand flank of the animal. This wound occurred some time prior to the most recent attacks, and additional attacks by cookie-cutter sharks may have retard- ed healing. It is notable that this older, larger wound occurs in the same position, but on the opposite side of the body, to the more recent on the right flank. This area may be a preferred site for attack by predators because the body shape and the projecting midline ridge forward of the caudal peduncle make it relatively easy to bite. Additionally, whale sharks often float at the surface to feed with their tails hang- ing below them to feed (Wilson, 2002). As white sharks are known to attack prey on the surface from below or behind (McCosker, 1985), the tail area may be more likely to be bitten (Long, 1991; Long and Jones, 1996). Such behavior is thought to account for the predominance of scars from white shark attacks in the region of the caudal peduncle of cetaceans (Long, 1991). The rear flanks may also be the body part that is presented to a predator by a whale shark fleeing attacks. While there are numerous accounts of white and tiger sharks scavenging whale carcasses (Randall, 1973; Pratt et al., 1982; McCosker, 1985; Springer and Gold, 1989; Bright, 2002), there are relatively few records of sharks attacking living megafauna approaching the size of this whale shark. An attack on a 3 m adult male , Mirounga angustirostris (, 1866) by a 4.7 m white shark was documented by Le Boeuf et al. (1982) and scars from shark attacks have been observed on adult humpback whales (Naessig and Lanyon, 2004). Shark attacks on adult whales may be common, but may go unnoticed by observers at the surface if they tend to occur on the underside and flanks of animals (Naessig and Lanyon, 2004). At approximately 5.5 m, the whale shark that was the subject of attacks at Ningaloo appears to be one of the largest living prey of sharks. These photographs are the first evidence of attacks by cookie cutter sharks on a whale shark. The bites by cookie cutter sharks were focused within the large healing wound inflicted on the left flank of the animal. Scars from cookie cutter sharks have not been recorded on other whale sharks at Ningaloo Reef and it seems likely that the tough skin of whale sharks may normally provide an effective defense from attacks NOTES 401 by these ectoparasites. Cookie cutter sharks have also been known to attack basking sharks, the temperate equivalent of the whale shark, but the location of bite marks on these animals was not specified (Tomas and Gomez, 1989). Despite their severity, this series of attacks was ultimately unsuccessful as the whale shark survived. Libraries of whale shark photographs collected at Ningaloo Reef from 1992 to 2004 show that 21% of sharks display scars that resemble bite marks (Press et al., Charles Darwin University, unpubl. data). This suggests that at- tacks on sharks may be relatively common, although it is unknown what proportion results in death. To date, fatal attacks on whale sharks by killer whales have been re- corded in the Gulf of California and whale shark pups have been found in the guts of marlin and a mako shark (Coleman, 1997). Attacks by top order predators thus may account for some of the life history traits of whale sharks such as the tough skin and deep layer of connective tissue on the dorsal surface of sharks. These attributes, and the great size of juvenile and adult whale sharks, may afford some degree of protec- tion from predation.

Acknowledgements

The authors thank S. Gibson, the Ningaloo Reef whale shark ecotourism industry, the De- partment of Conservation and Land Management (Exmouth), and an anonymous person for donating the photos in Figures 1 and 2. We also thank J. Stevens and G. Taylor and two anony- mous reviewers for comments on draft versions of this manuscript.

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Date Submitted: 27 July, 2005. Date Accepted: 15 November, 2005.

Addresses: University of Western Australia, School of Plant Biology, 35 Stirling Highway, Crawley, WA, 6009 Australia. E-mail: . (M.M.) Australian Insti- tute of Marine Science, PO Box 40197, Casuarina MC, Northern Territory 0811 Australia. (A.R.) WWF Australia, PO Box 293, Exmouth Western Australia, 6707 Australia.