Space Utilization and Swimming Depth of White Sharks, Carcharodon carcharias, at the South Farallon Islands, Central California

This paper presents information on the movements of white sharks, Carcharodon carcharias, at the South Farallon Islands (SFI), central California. Acoustic telemetry techniques provided preliminary data on the diurnal space utilization, movement patterns and swimming depths of four white sharks, ranging from approximately 3.7 to 4.9m in length. Sharks swam within about 10m of the bottom to depths of approximately 30m, but in deeper water they tended to stray more from the bottom. Activity spaces for time periods tracked ranged from 1.84 to 9.15km². Indications are that an inverse relationship exists between length and activity space. During the time tracked, larger individuals swam within particular areas around the islands whereas smaller individuals did not restrict their movements in the same manner. Values of a site attachment index were inversely related to length for all sharks tracked. The site attachment indices, apparent inverse relationship between total length and activity space and observations on telemetered and other known individuals support a hypothesis that larger sharks possess site fidelity in their search for prey at SFI, within and between years. With the high frequency of predation by white sharks on juvenile northern elephant seals at SFI in the fall, the majority of the sharks' movements are probably related to their search for these pinniped prey. These data provide preliminary evidence that white sharks at SFI may search for prey by swimming in a particular area over a number of days or weeks, traversing the area in a manner which maximizes coverage, and swimming close to the bottom or at a distance far enough from the surface to remain cryptic from prey.     

Telemetry and Satellite Tracking of Whale Sharks, Rhincodon Typus, in the Sea of Cortez, Mexico, and the North Pacific Ocean

We used satellite-linked radio telemetry to document the geographic and vertical movements and thermal habitats of whale sharks in the Sea of Cortez and as they migrated into the north Pacific Ocean. Of 17 sharks tagged between 1994 and 1996, six dispersed widely in the Sea of Cortez during 12–39 days of tracking. Four others left the Sea of Cortez and ranged extensively in the north Pacific Ocean. Indeed, one whale shark migrated to the western north Pacific Ocean, covering over 13000km in 37 months of tracking. The sharks generally occupied areas where sea surface water temperatures were between 28 and 32°C, though several ranged to depths of 240m or deeper where water temperature reached 10°C or colder. Whale sharks may segregate by size and sex, and their movement patterns appear to be related to oceanographic features, such as sea mounts and boundary currents, where primary productivity may be enhanced. These results have important implications for the global conservation of the world's largest yet least known fish. We think that satellite telemetry is a exceptionally promising tool for learning more about the ecology of whale sharks, especially when combined with conventional methods of telemetry and molecular biology.authorship arranged alphabetically     

Tractable models for testing theories about natural strategies: foraging behaviour and habitat selection of free‐ranging sharks

Marine and terrestrial environments differ fundamentally in space‐time scales of both physical and ecological processes. These differences will have an impact on the animals inhabiting each domain, particularly with respect to their spatial ecology. The behavioural strategies that underpin observed distributions of marine species are therefore important to consider. Comparatively little is known, however, about how wild fishes actually respond to gradients in food supply and temperature, and to potential mates. This paper describes how behavioural theory is being used to elucidate the strategies and tactics of free‐ranging sharks in three specific areas of study, namely, foraging on zooplankton, behavioural energetics and sexual segregation. The studies discussed are novel because shark movements were tracked in the wild using electronic tags in relation to simultaneous measurements of prey densities and thermal resources. The results show that filter‐feeding (basking shark, Cetorhinus maximus ) and predatory (dogfish, Scyliorhinus canicula ) sharks have relatively complex behaviour patterns integrally linked to maximizing surplus power, often through making short and longer term 'trade‐off' decisions between optimal foraging and thermal habitats. Interestingly, female S. canicula exhibit alternative behavioural strategies compared to males, a difference resulting in spatial segregation by habitat. Sexual segregation in this species occurs primarily as a consequence of male avoidance by females. Studies on free‐ranging sharks provide a useful model system for examining how a predator's strategy is shaped by its environment. More theory‐based studies of the behavioural processes of sharks are required however, before critical comparisons with other vertebrate predators are possible. Suggestions for further research to address this knowledge gap are given.     

On the Origins of the Spanish Word ‘tiburón’, and the english word ‘shark’

Large sharks were known to the Greeks and Romans, and references to large sharks of the Mediterranean are found in the writings of classical writers. However, large sharks are conspicuously absent from the medieval bestiaries that described the then known fauna. The explanation for this interesting omission is simple: Medieval man did not encounter large sharks because he fished mainly in rivers and close to shore and did not venture far into the ocean to catch fish, and the few large European sharks did not venture into rivers or shallow waters. The Spanish and the English first encountered large sharks in the American tropics. Both groups borrowed Amerindian words to designate them. The Spanish borrowed the word tiburón from the Carib Indians, and, later, the English borrowed tiburón from the Spanish and used it for about 100 years. In the late sixteenth century, the English borrowed the word xoc from the Mayans and it became the English word shark.     

Estimation of Shark Home Ranges using Passive Monitoring Techniques

We examined a population of blacktip sharks, Carcharhinus limbatus, within a coastal nursery area to define how individuals use the nursery habitat throughout the summer. We used a series of acoustic hydrophones to passively monitor the movement patterns of sharks for periods up to 167 days. We used passive monitoring data to calculate home range estimates using minimum convex polygon (MCP) and fixed kernel estimators. MCP calculated the extent of an individual's range. Kernel estimates provided information regarding the utilization of space within the home range including core area (50% kernel) and larger excursions outside the core area (95% kernel). Individuals within the nursery area typically used a consistently small core area. All sharks monitored in the study site underwent a home range expansion during the month of July, suggesting a synchronous population-level change in habitat use. This change in habitat use was reflected in all home range calculations. Passive monitoring revealed that young sharks remain within the nursery area for up to 6 months. The long-term use of this nursery area reflects its critical importance to young blacktip sharks.     

Insights into Young of the Year White Shark, Carcharodon carcharias, Behavior in the Southern California Bight

A young of the year female white shark, Carcharodon carcharias, was tagged with a pop-up satellite archival tag off Southern California in early June of 2000. The tag was recovered after 28 days, and records of temperature, depth and light intensity were extracted. Depth and temperature records indicate a number of interesting behaviors, including a strong diurnal pattern. At night the shark remained in the top 50 m, often making shallow repetitive vertical excursions. Most dives below the mixed layer were observed during the day, 91% of which occurred from 05:00 to 21:00 h, with depths extending to 240 m. Many of the dives exhibited secondary vertical movements that were consistent with the shark swimming at the bottom (at depths from 9 to 165 m) where it was most likely foraging. The white shark experienced dramatic and rapid changes in temperature, and demonstrated a considerable tolerance for cold waters. Temperatures ranged from 9°C to 22°C, and although 89% of the total time was spent in waters 16–22°C, on some days the small shark spent as much as 32% of the time in 12°C waters. The deep dives into cold waters separate the white sharks from mako sharks, which share the California Bight nursery ground but appear to remain primarily in the mixed layer and thermocline. Movement information (derived from light-based geolocation, bottom depths and sea surface temperatures) indicated that the white shark spent the 28 days in the Southern California Bight, possibly moving as far south as San Diego, California. While the abundance and diversity of prey, warm water and separation from adults make this region an ideal nursery ground, the potential for interaction with the local fisheries should be examined.     

Short-term Movements of Juvenile and Neonate Sandbar Sharks, Carcharhinus plumbeus, on their Nursery Grounds in Delaware Bay

We investigated short-term movements of neonate and juvenile sandbar sharks, Carcharhinus plumbeus, on their nursery grounds in Delaware Bay. The majority of sharks tracked limited their movements to water less than 5m deep, remained within 5km of the coastline, and occupied oblong activity spaces along the coast. In addition to site-attached coastal movements observed, several sharks moved entirely across Delaware Bay or spent considerable time in deeper portions of the central bay. Sharks tracked on the New Jersey side of the bay tended to spend more time in deeper water, farther from shore than sharks tracked on the Delaware side. Observation-area curves estimated that optimal tracking time for sandbar sharks in Delaware Bay was 41h. Indices of site attachment showed that movement patterns of tracked sandbar sharks varied from nomadic to home ranging. There was no significant difference in rate of movement for day/night, crepuscular periods, or between juveniles and neonates. In general, young sandbar sharks patrolled the coast and appeared to be site attached to some extent, but were capable of making longer excursions, including movement entirely across Delaware Bay.