Tag: sharks of north carolina

  • Beyond the Horizon: The Pelagic Sharks Off Onslow County

    Beyond the Horizon: The Pelagic Sharks Off Onslow County

    Most people standing on the beach watch the Atlantic as though the ocean ends where detail disappears.

    Nearshore water is easy to read. Pelicans diving offshore reveal where baitfish have gathered near the surface. The first sea turtle crawls of the season begin appearing along the upper beach. Sandbars reveal themselves through shifting wave patterns and changes in water color.  Even when the water is murky, the coastline still feels structured because the movement happening near shore leaves visible clues.

    Farther offshore, those visible clues become harder to read.

    Beyond the breakers, past the shrimp boats and distant military vessels that sometimes mark the horizon, the Atlantic off Onslow County drops across the continental shelf into deeper pelagic water. From shore, that open water can appear empty simply because most of its structure is hidden beneath distance, depth, and moving currents. But the offshore ocean is highly organized. Temperature layers separate water masses. Squid and fish rise toward the surface at night and descend again before daylight. Currents gather plankton and compress bait schools into dense patches of life that may stretch for miles before dissolving again.

    And moving through those shifting layers are sharks most beachgoers never see.

    Species like the bigeye thresher shark, scalloped hammerhead, Carolina hammerhead, smooth hammerhead, great hammerhead, and tiger shark all occupy different parts of the same Atlantic system connected to North Carolina’s coast. They are not interchangeable predators simply sharing the same water. Each species is specialized for a different way of hunting, sensing, and moving through the pelagic environment.

    Even though most people never see these sharks directly, their influence does not remain offshore.

    They work their way back toward the coast through changes in prey behavior, bait distribution, migration timing, and the balance of the food web itself.

    The Shark Built for Dim Water

    The bigeye thresher shark (Alopias superciliosus) does not resemble most sharks people imagine from coastal documentaries or fishing piers. Its eyes are unusually large, and nearly half of its body length is tail.

    A bigeye thresher shark (Alopias superciliosus) moves through dim offshore Atlantic water beyond the Carolina coast. Its enlarged eyes help it hunt in low light, while its elongated tail can be used to stun schooling prey before feeding. | Image credit: NC Sea Grant
    A bigeye thresher shark (Alopias superciliosus) moves through dim offshore Atlantic water beyond the Carolina coast. Its enlarged eyes help it hunt in low light, while its elongated tail can be used to stun schooling prey before feeding. | Image credit: NC Sea Grant

    Both features are tied directly to life in deeper offshore water.

    Bigeye threshers spend much of their time moving vertically through the water column, often descending into dim water during daylight hours and returning closer to the surface at night as squid and mesopelagic fish migrate upward under darkness (Weng & Block, 2004). Offshore pelagic systems are layered environments. Light fades rapidly with depth, and many prey species spend daylight hours far below the surface where visibility is limited.

    The shark’s large eyes help gather more available light in those darker layers.

    For someone standing on the beach at sunset, the horizon still appears bright. Offshore, hundreds of feet below the surface, the bigeye thresher is already hunting in water where daylight barely penetrates.

    Its tail is equally specialized. Schooling fish survive by moving together in synchronized motion, creating confusion for predators trying to isolate individual prey. The elongated upper lobe of the thresher’s tail evolved as a way to disrupt that coordination. Researchers have documented threshers using powerful overhead tail strikes to stun schooling fish before circling back to feed (Oliver et al., 2013).

    That hunting strategy matters ecologically because the species targeted by threshers are often highly connected to broader Atlantic food webs. Squid, mackerel, and schooling pelagic fish move energy between offshore and coastal systems. Large predators help regulate those populations and alter how tightly schools gather, where they move, and how heavily they feed on smaller forage species beneath them in the food web (Heithaus et al., 2008).

    Without predators thinning and disrupting those mid-level prey schools, feeding pressure shifts downward. Larger populations of squid and predatory fish consume more small forage species, including baitfish that later support seabirds, larger fish, and predators closer to shore. The result is not an empty ocean, but a gradual reorganization of how energy moves through the coastal ecosystem.

    What beachgoers may eventually notice are changes in feeding activity: fewer concentrated bird flocks offshore, shifting bait movements, or less predictable surface eruptions beyond the breakers.

    The Sharks That Hunt Electricity

    Hammerheads occupy a different sensory world than most coastal predators.

    The broad hammer-shaped head shared by species like the scalloped hammerhead, great hammerhead, smooth hammerhead, and Carolina hammerhead is called a cephalofoil. Spread across that wide structure are sensory pores known as ampullae of Lorenzini, specialized organs capable of detecting weak electrical fields produced by other animals (Kajiura, 2001).

    Every muscle contraction and heartbeat generated by prey produces tiny electrical signals in the water.

    A stingray buried beneath sand may be invisible to a human observer, but to a hammerhead it is still broadcasting electrical information.

    The widened head helps the shark compare those signals across a broader sensory field, improving directional accuracy while hunting. Scientists have compared shark electroreception to detecting the output of a small household battery from extraordinary distances under ideal conditions, though in the ocean the system functions at close range to help sharks pinpoint hidden prey.

    While beachgoers scan the water looking for dorsal fins, hammerheads are effectively scanning the seafloor for living electrical currents.

    That sensory adaptation helps explain why multiple hammerhead species can occupy overlapping Atlantic waters without performing identical ecological roles.

    The Offshore Traveler

    The scalloped hammerhead (Sphyrna lewini) is one of the more oceanic hammerhead species associated with continental shelf edges, offshore structures, and migratory routes through deeper Atlantic water (Klimley, 1993).

    A scalloped hammerhead shark (Sphyrna lewini) moves through offshore Atlantic water beyond the Carolina coast. The broad cephalofoil spreading from its head contains electroreceptors capable of detecting faint electrical signals produced by prey hidden beneath sand and low-visibility water. | Image credit: A. Murch
    A scalloped hammerhead shark (Sphyrna lewini) moves through offshore Atlantic water beyond the Carolina coast. The broad cephalofoil spreading from its head contains electroreceptors capable of detecting faint electrical signals produced by prey hidden beneath sand and low-visibility water. | Image credit: A. Murch

    Scalloped hammerheads often move in schools, particularly when younger, and feed heavily on fish, squid, and smaller sharks. Their body shape and behavior are well suited for highly mobile pelagic hunting where prey concentrations shift constantly with temperature and current boundaries.

    They are not simply “using deeper water.” They are adapted to a system where the structure itself is always moving.

    Warm and cool water masses sliding against one another can compress bait into narrow feeding corridors. Squid rise toward the surface after dark. Pelagic fish move vertically and horizontally depending on light levels and prey availability. The scalloped hammerhead’s movement patterns mirror that instability.

    Because they occupy such mobile offshore environments, scalloped hammerheads help regulate prey populations across broad sections of the continental shelf rather than within a single localized habitat.

    The Hidden Hammerhead

    For decades, scientists believed many hammerheads moving through the western Atlantic belonged to the same species.

    But the Carolina hammerhead (Sphyrna gilberti) had likely been there the entire time unnoticed.

    Researchers eventually discovered that some sharks identified as scalloped hammerheads were genetically distinct and consistently possessed fewer vertebrae, revealing that two separate species had been moving through the same waters unnoticed (Quattro et al., 2013).

    Radiographs of the Carolina hammerhead (Sphyrna gilberti) helped reveal that a second hammerhead species had been moving through western Atlantic waters largely unnoticed. Although visually similar to the scalloped hammerhead, skeletal differences and genetic analysis confirmed the Carolina hammerhead as a distinct species in 2013. | Image credit: J. Quattro et al., 2013 (left); S. Raredon, Smithsonian Institution, National Museum of Natural History (right)Radiographs of the Carolina hammerhead (Sphyrna gilberti) helped reveal that a second hammerhead species had been moving through western Atlantic waters largely unnoticed. Although visually similar to the scalloped hammerhead, skeletal differences and genetic analysis confirmed the Carolina hammerhead as a distinct species in 2013. | Image credit: J. Quattro et al., 2013 (left); S. Raredon, Smithsonian Institution, National Museum of Natural History (right)
    Radiographs of the Carolina hammerhead (Sphyrna gilberti) (left) helped reveal that a second hammerhead species had been moving through western Atlantic waters largely unnoticed. Although visually similar to the scalloped hammerhead (right), skeletal differences and genetic analysis confirmed the Carolina hammerhead as a distinct species in 2013. | Image credit: J. Quattro et al., 2013 (left); S. Raredon, Smithsonian Institution, National Museum of Natural History (right)

    The discovery revealed that even sharks moving through the same Atlantic waters were more specialized than they first appeared.

    From the beach, the offshore Atlantic often appears open and uniform because distance hides most of its detail. But even scientists were still uncovering hidden structures within those waters. Sharks that looked nearly identical from the surface were occupying the same coastline as separate species with potentially different ecological roles.

    The Carolina hammerhead still overlaps geographically with other hammerheads along the southeastern United States, and researchers are continuing to study how those species divide habitat, prey, and movement through the Atlantic.

    For beachgoers, the discovery is a reminder that the Atlantic beyond the breakers is more ecologically layered than it first appears, with multiple shark species occupying waters that can look uniform from shore. 

    The Ray Hunter

    The great hammerhead (Sphyrna mokarran) occupies a different ecological role than its smaller relatives.

    A great hammerhead shark (Sphyrna mokarran) moves through offshore water. The species is highly specialized for hunting rays, using its broad cephalofoil to improve maneuverability and detect prey hidden along the seafloor. | Image credit: Oregon State University
    A great hammerhead shark (Sphyrna mokarran) moves through offshore water. The species is highly specialized for hunting rays, using its broad cephalofoil to improve maneuverability and detect prey hidden along the seafloor. | Image credit: Oregon State University

    Great hammerheads are more solitary and strongly associated with rays, including stingrays and cownose rays. Their cephalofoil is not simply a sensory structure. It also improves maneuverability and may help pin rays against the seafloor during feeding attempts (Strong et al., 1990).

    That specialization matters because rays themselves strongly influence coastal ecosystems.

    Rays such as cownose rays and Atlantic stingrays disturb sediment, expose buried organisms, and alter benthic communities while feeding across shallow coastal bottoms. Great hammerheads help regulate those ray populations and influence where rays spend time feeding.

    Great hammerheads influence more than the number of rays moving through coastal habitats.  The presence of large predators changes prey behavior as well. Rays may avoid lingering in exposed feeding areas when hammerheads are nearby, redistributing feeding pressure across habitats.

    For beachgoers, those ecological effects may eventually appear through changes in ray abundance, feeding activity, or shifting patterns of disturbed sediment along shallow coastal waters.

    The Cooler-Water Hunter

    The smooth hammerhead (Sphyrna zygaena) can look, at first glance, like another variation of the same hammerhead design.

    But its head gives away part of its story.

    Unlike the scalloped hammerhead, the smooth hammerhead lacks the central notch along the front edge of the cephalofoil. That difference may seem small to a casual observer, but it reflects a separate species adapted to a somewhat different part of the Atlantic system. Smooth hammerheads are often associated with cooler temperate waters and feed heavily on schooling fish and cephalopods moving through offshore shelf waters (Compagno, 2001).

    A smooth hammerhead shark (Sphyrna zygaena) moves through open offshore water. Unlike the scalloped hammerhead, the smooth hammerhead lacks the central notch along the front edge of the cephalofoil and is more commonly associated with cooler temperate waters and schooling prey along the continental shelf. | Image credit: S. Judd
    A smooth hammerhead shark (Sphyrna zygaena) moves through open offshore water. Unlike the scalloped hammerhead, the smooth hammerhead lacks the central notch along the front edge of the cephalofoil and is more commonly associated with cooler temperate waters and schooling prey along the continental shelf. | Image credit: S. Judd

    That specialization matters because schooling fish and squid help move energy through the open Atlantic.

    These prey species do not stay fixed in one place. They shift with temperature, currents, light, and season, gathering in patches that may appear briefly before dispersing again. Smooth hammerheads are part of the predator community that follows and regulates that movement through cooler portions of the continental shelf.

    The relationship is not simply a shark chasing fish through open water. By feeding within those moving schools, smooth hammerheads help shape how prey gathers, how long those schools remain concentrated, and how much pressure they place on smaller forage species below them in the food web.

    For beachgoers, those ecological effects may eventually appear through seasonal changes in bait movement, bird activity, or the mix of predators feeding along the shelf as offshore waters warm and cool through the year.

    The Shark That Connects Habitats

    Few sharks move between offshore and coastal systems as fluidly as the tiger shark.

    Tiger sharks (Galeocerdo cuvier) are often reduced in public imagination to sensational headlines or descriptions as “garbage eaters,” largely because of their opportunistic feeding behavior and willingness to consume a wide range of prey.

    But ecological flexibility is precisely what makes them important.

    A tiger shark (Galeocerdo cuvier) moves through tropical offshore water. Tiger sharks travel between offshore habitats, shoals, and coastal systems following seasonal prey movements, linking distant parts of the Atlantic food web through their wide-ranging movements and opportunistic feeding behavior. | Image credit: Fishes of Sarasota County, FL
    A tiger shark (Galeocerdo cuvier) moves through tropical offshore water. Tiger sharks travel between offshore habitats, shoals, and coastal systems following seasonal prey movements, linking distant parts of the Atlantic food web through their wide-ranging movements and opportunistic feeding behavior. | Image credit: Fishes of Sarasota County, FL

    Tiger sharks move between offshore waters, shoals, nearshore habitats, and sometimes estuarine environments following seasonal prey movements and temperature shifts (Heithaus, 2001). Sea turtles, rays, fish, carrion, and other prey species all become part of that broader movement pattern.

    Their presence changes how other animals use the same habitats.

    Sea turtles may avoid grazing too heavily in exposed areas when tiger sharks are nearby. Rays redistribute feeding activity. Schools of fish alter where they gather. The presence of a large predator changes how long prey species remain in one place and how intensely they feed before moving on. Areas that might otherwise experience constant grazing or disturbance begin receiving periods of recovery as animals move more cautiously through the habitat (Heithaus et al., 2008). 

    That movement connects habitats that people often think of as separate parts of the ocean.

    A tiger shark feeding offshore may later move closer to shoals, estuaries, or coastal waters as prey shifts with season and temperature. The same predator influencing sea turtle grazing patterns offshore may eventually pass along the edges of bait schools closer to shore weeks later.

    For beachgoers, those connections may appear through changing patterns of sea turtle activity, shifting schools of fish near the breakers, or the seasonal movement of predators along the Carolina coast.

    The Sharks People Talk About Most

    Not all sharks connected to Onslow County remain far offshore.

    Species like the great white shark and bull shark tend to dominate public attention because they are more familiar through media coverage and coastal sightings. Tagged great whites moving along the Atlantic coast frequently make headlines, while sharks seen near inlets or murky water are often assumed to be bull sharks whether identification is confirmed or not.

    But those assumptions can flatten the complexity of the coastal ecosystem.

    Bull sharks (Carcharhinus leucas) are well known for their ability to tolerate freshwater, but they are not the only sharks capable of handling changing salinity. Along the Carolina coast, species such as bonnetheads and juvenile hammerheads also use estuarine environments where tides, rainfall, and river flow constantly shift the balance between salt and fresh water. Coastal systems are not divided into simple categories of “ocean” and “freshwater.” They are gradients, and many sharks are adapted to move through those changing conditions. 

    A bull shark (Carcharhinus leucas) moves through offshore water accompanied by remoras. Although bull sharks are known for their ability to tolerate lower salinity and move into estuaries and rivers, they are also highly mobile coastal and offshore predators that regularly travel through marine waters along the Atlantic coast. | Image credit: B. Skinstad
    A bull shark (Carcharhinus leucas) moves through offshore water accompanied by remoras. Although bull sharks are known for their ability to tolerate lower salinity and move into estuaries and rivers, they are also highly mobile coastal and offshore predators that regularly travel through marine waters along the Atlantic coast. | Image credit: B. Skinstad

    Great whites (Carcharodon carcharias), meanwhile, are often discussed as solitary coastal hunters, but along the western Atlantic they are also highly migratory predators tied to seasonal prey movements, temperature ranges, and offshore habitats (Block et al., 2011).

    A great white shark (Carcharodon carcharias) moves through open offshore water. Great whites are highly migratory predators capable of traveling vast distances between offshore habitats and productive coastal feeding grounds, linking distant regions of the Atlantic and Pacific through seasonal movement. | Image credit: E. Levy
    A great white shark (Carcharodon carcharias) moves through open offshore water. Great whites are highly migratory predators capable of traveling vast distances between offshore habitats and productive coastal feeding grounds, linking distant regions of the Atlantic and Pacific through seasonal movement. | Image credit: E. Levy

    Both species are part of the broader Atlantic system connected to North Carolina’s coast, but the sharks occupying pelagic waters beyond the visible horizon often receive far less attention despite shaping offshore food webs just as strongly.

    Why Recovery Takes So Long

    Many fish species along the Carolina coast mature quickly and reproduce in enormous numbers. Menhaden, mullet, and other forage fish may begin reproducing within only a few years while releasing hundreds of thousands—or even millions—of eggs.

    Large sharks follow a very different strategy.

    Species like great hammerheads, tiger sharks, and threshers often require more than a decade to reach reproductive maturity, and they produce far fewer offspring than most bony fish (Cortés, 2000). Some large female sharks may spend well over a decade surviving storms, fishing pressure, predators, disease, and changing ocean conditions before producing pups for the first time.

    That slower reproductive strategy evolved partly because large sharks occupy upper levels of the food web where adults face relatively few natural predators. Evolution favored longer lifespans, slower growth, and fewer offspring with higher survival chances.

    But the same strategy creates vulnerability.

    A fish population capable of reproducing within two or three years can rebound relatively quickly after declines. A shark population that requires fifteen years or more to produce breeding adults cannot.

    The offshore Atlantic built these predators slowly.

    And when populations decline, recovery happens slowly as well.

    Why More Sightings Do Not Always Mean More Sharks

    For many people along the Carolina coast, sharks can feel more visible now than they did decades ago.

    Drone footage from the North Carolina coast reveals how modern technology now captures shark movement near beaches that would have gone largely unseen from shore only a few decades ago. Increased visibility does not necessarily mean sharks are suddenly overwhelming coastal waters, but it does change how people perceive the Atlantic around them. | Image credit: L. Abed
    Drone footage from the North Carolina coast reveals how modern technology now captures shark movement near beaches that would have gone largely unseen from shore only a few decades ago. Increased visibility does not necessarily mean sharks are suddenly overwhelming coastal waters, but it does change how people perceive the Atlantic around them. | Image credit: L. Abed

    Anglers report more sharks taking hooked fish before they can be reeled in, a behavior known as depredation. Drone footage captures feeding activity that would have gone unseen from shore years ago. Social media spreads sightings quickly, sometimes creating the impression that sharks are suddenly overwhelming coastal waters.

    Some shark populations have shown signs of recovery following decades of decline and changing fishing regulations. Long-time fishers noticing more shark encounters in certain areas may not be imagining it. In some cases, there likely are more sharks present than there were during periods of heavier population decline in the late twentieth century.

    But recovery is not the same as overabundance.

    Forty years ago, far fewer people were fishing offshore, kayaking through estuaries, filming the surf with drones, or posting shark encounters online in real time. Coastal waters are now observed more continuously than at any point in history, while recreational fishing activity itself creates more opportunities for sharks and people to interact.

    Even with signs of recovery, many large shark species along the Atlantic coast still exist at a fraction of the population levels seen before major declines in the late twentieth century (Baum et al., 2003; Worm et al., 2013). 

    A true overabundance of large predators would likely look very different along the Carolina coast. Bait schools would become harder to find, feeding activity along the surface would begin thinning out, and predators would increasingly compete over limited prey. Instead, much of what people are witnessing today is the overlap between recovering shark populations, concentrated recreational fishing activity, and a coastline watched more closely than ever before (Heithaus et al., 2008). 

    For beachgoers, that change can make sharks feel suddenly more common, even as many offshore ecosystems are still rebuilding from declines that unfolded over generations.

    What Changes Along the Coast When They Decline

    By the time most people arrive at the beach in summer, the offshore system is already in motion.

    Pelicans are not simply following random schools of fish. The bait moving through the breakers may have spent weeks feeding along temperature boundaries farther offshore. Rays passing through the shallows are connected to predators that hunt them beyond the visible edge of the continental shelf. Squid rising toward the surface at night become part of a food web that stretches from deep Atlantic water back toward the surf zone.

    Most of those connections remain invisible from shore.

    A person standing on the beach cannot see a bigeye thresher moving through dim offshore water hundreds of feet below the surface, or a hammerhead sweeping across the bottom searching for the electrical signals of buried prey. They cannot see tiger sharks shifting between offshore and coastal habitats as water temperatures change through the season.

    But those predators still influence what eventually reaches the coastline.

    The schools of fish birds gather over, the movement of rays through shallow water, the distribution of predators and prey along the continental shelf, and even the timing of seasonal feeding activity are tied to an offshore ecosystem organized partly by sharks most people never encounter directly.

    From the beach, the Atlantic often appears flat and open beyond the horizon.

    In reality, it is layered with movement, specialization, and predators adapted to parts of the ocean most people never realize are there.

    What the Horizon Conceals

    From the beach, the Atlantic often appears flat and empty beyond the breakers. Most people will never see a bigeye thresher rising from dim offshore water or a hammerhead sweeping across the continental shelf searching for prey hidden beneath the sand. The larger structure of the pelagic Atlantic remains mostly invisible from shore.

    But the absence of visibility is not the same as absence of life.

    Far beyond the swimming beaches and nearshore bars, sharks continue moving through layered offshore habitats shaped by depth, temperature, migration, and prey. Some travel between offshore waters and shoals. Others patrol deeper pelagic systems where sunlight fades and the surface reveals little of what exists below.

    Those movements eventually connect back to the coast itself.

    The same Atlantic that carries sea turtle hatchlings past the breakers, pushes baitfish toward the shoreline, and gathers pelicans over feeding fish also extends outward into a far larger offshore ecosystem organized by predators most people never see directly.

    The horizon does not separate the beach from another ocean.

    It only marks the point where the visible Atlantic gives way to the hidden one.

    Even from the shoreline, the Atlantic extends into a far larger offshore ecosystem shaped by predators, migration, depth, and movement beyond what can easily be seen from shore. The horizon does not mark the end of the ocean’s structure, only the limit of what we can observe from the beach. | Image credit: A. Mitchell
    Even from the shoreline, the Atlantic extends into a far larger offshore ecosystem shaped by predators, migration, depth, and movement beyond what can easily be seen from shore. The horizon does not mark the end of the ocean’s structure, only the limit of what we can observe from the beach. | Image credit: A. Mitchell

    References

    Baum, J. K., Myers, R. A., Kehler, D. G., Worm, B., Harley, S. J., & Doherty, P. A. (2003). Collapse and conservation of shark populations in the Northwest Atlantic. Science, 299(5605), 389-392. https://doi.org/10.1126/science.1079777

    Block, B. A., Jonsen, I. D., Jorgensen, S. J., Winship, A. J., Shaffer, S. A., Bograd, S. J., Hazen, E. L., Foley, D. G., Breed, G. A., Harrison, A., Ganong, J. E., Swithenbank, A., Castleton, M., Dewar, H., Mate, B. R., Shillinger, G. L., Schaefer, K. M., Benson, S. R., Weise, M. J., … Costa, D. P. (2011). Tracking APEX marine predator movements in a dynamic ocean. Nature, 475(7354), 86-90. https://doi.org/10.1038/nature10082

    Compagno, L. J. (2001). Sharks of the world: An annotated and illustrated catalogue of shark species known to date (2nd ed.). Food and Agriculture Organization of the United Nations.

    Cortés, E. (2000). Life history patterns and correlations in Sharks. Reviews in Fisheries Science, 8(4), 299-344. https://doi.org/10.1080/10408340308951115

    Heithaus, M. R. (2001). The biology of tiger sharks, Galeocerdo Cuvier, in Shark Bay, Western Australia: Sex ratio, size distribution, diet, and seasonal changes in catch rates. Environmental Biology of Fishes, 61(1), 25-36. https://doi.org/10.1023/a:1011021210685

    Heithaus, M. R., Frid, A., Wirsing, A. J., & Worm, B. (2008). Predicting ecological consequences of marine top predator declines. Trends in Ecology & Evolution, 23(4), 202-210. https://doi.org/10.1016/j.tree.2008.01.003

    Kajiura, S. M. (2001). Head morphology and Electrosensory pore distribution of Carcharhinid and Sphyrnid sharks. Environmental Biology of Fishes, 61(2), 125-133. https://doi.org/10.1023/a:1011028312787

    Klimley, A. P. (1993). The Behavior and Ecology of the Scalloped Hammerhead Shark. Stanford University Press.

    Musick, J. A., Burgess, G., Cailliet, G., Camhi, M., & Fordham, S. (2000). Management of sharks and their relatives (Elasmobranchii). Fisheries, 25(3), 9-13. https://doi.org/10.1577/1548-8446(2000)025<0009:mosatr>2.0.co;2

    Oliver, S. P., Turner, J. R., Gann, K., Silvosa, M., & D’Urban Jackson, T. (2013). Thresher sharks use tail-slaps as a hunting strategy. PLoS ONE, 8(7), e67380. https://doi.org/10.1371/journal.pone.0067380

    Quattro, J. M., Driggers, W. B., Grady, J. M., Ulrich, G. F., & Roberts, M. A. (2013). Sphyrna gilberti, a new hammerhead shark (Carcharhiniformes, Sphyrnidae) from the western Atlantic Ocean. Zootaxa, 3702(2), 159. https://doi.org/10.11646/zootaxa.3702.2.5

    Sims, D. W. (2006). Differences in habitat selection and reproductive strategies of male and female sharks. Sexual Segregation in Vertebrates, 127-147. https://doi.org/10.1017/cbo9780511525629.009

    Strong, W. R., Snelson, F. F., & Gruber, S. H. (1990). Hammerhead shark predation on Stingrays: An observation of prey handling by Sphyrna mokarran. Copeia, 1990(3), 836. https://doi.org/10.2307/1446449

    Weng, K. C., & Block, B. A. (2004). Diel vertical migration of the bigeye thresher shark (Alopias superciliosus), a species possessing orbital retia mirabilia (102:221–229). NMFS Scientific Publications Offic. https://spo.nmfs.noaa.gov/sites/default/files/pdf-content/2004/1021/weng.pdf

    Worm, B., Davis, B., Kettemer, L., Ward-Paige, C. A., Chapman, D., Heithaus, M. R., Kessel, S. T., & Gruber, S. H. (2013). Global catches, exploitation rates, and rebuilding options for sharks.

  • Reader Request: Cookiecutter Sharks and the Evidence They Leave Behind

    Reader Request: Cookiecutter Sharks and the Evidence They Leave Behind

    This post comes from a reader’s question sent in as our season has shifted toward winter: Can you tell me more about cookiecutter sharks—their life history, diet, and range—and do we have any evidence of them connected to our area? It’s a winter question, shaped by migration and distance. Cookiecutter sharks are not animals we expect to see off the beach or inside our estuaries. But their story does brush our coast—quietly and indirectly—on the bodies of animals that move past North Carolina each year.

    Cookiecutter sharks are small, elusive, and rarely observed alive. Yet their marks travel widely, carried northward along offshore pathways that tighten in winter, when the Gulf Stream draws migratory lives closer to our horizon.

    A small shark with a global range

    Cookiecutter sharks belong to the genus Isistius, with Isistius brasiliensis the most widely documented species in the Atlantic. Adults are typically 40–60 cm (15.7-23.6 in) long, with a compact, cylindrical body and proportionally large eyes adapted for low-light conditions (Compagno, 1984). Despite their size, their distribution is vast. They occur circumglobally in tropical and subtropical oceans and are strongly associated with pelagic, offshore environments rather than continental shelves or coastal waters (Compagno, 1984; Papastamatiou et al., 2010).

    Most of a cookiecutter shark’s life unfolds far from shore and largely out of sight. This is one reason they remain poorly known to the public, even as their ecological footprint spans entire ocean basins.

    Morphology built for taking a piece

    The cookiecutter shark’s reputation comes from a feeding strategy unlike that of any other shark. Thick, muscular lips create a suction seal against prey, while the lower jaw carries a single row of large, triangular teeth fused into a continuous cutting blade. These lower teeth are shed as a single unit, maintaining an efficient cutting edge throughout the shark’s life (Compagno, 1984).

    During feeding, the shark attaches briefly, anchors with its upper teeth, and rotates its body to excise a plug of tissue. The result is a circular or oval wound with clean margins—so precise it can look manufactured rather than bitten (Papastamatiou et al., 2010). This strategy allows a small shark to feed on animals far larger than itself without prolonged pursuit or lethal force.

    Photos of cookiecutter shark teeth and jaws
    Cookiecutter shark jaws and teeth | Photo credits (from left to right): The Australian Museum (2022); Grant Museum of Zoology. LDUCZ-V415; Smithsonian Institute

    Diet and trophic role in the open ocean

    Cookiecutter sharks feed across a wide range of pelagic organisms. Documented prey include tunas, swordfish, other large teleost fishes, squids, dolphins, and large whales (Muñoz-Chápuli et al., 1988; Niella et al., 2018; Best et al., 2016). Rather than functioning as apex predators, they act as ectoparasitic predators—removing tissue while leaving prey alive. Chemical tracer and stable isotope analyses place Isistius species at relatively high trophic positions despite their small size, integrating energy from multiple pelagic food webs (Carlisle et al., 2021). Their influence is subtle but widespread, written not in dramatic predation events but in repeated, measurable interactions across the open ocean.

    Life in the vertical: behavior and movement

    Cookiecutter sharks are closely associated with diel vertical migration. During daylight hours, they occupy deeper mesopelagic waters; at night, they ascend toward the surface as fishes and marine mammals rise to feed (Papastamatiou et al., 2010). This nightly overlap increases encounter rates with large, fast-moving prey under low-light conditions.

    This behavior explains both their effectiveness and their invisibility. Cookiecutter sharks rarely interact directly with humans, and most evidence of their presence comes not from sightings, but from the wounds they leave behind.

    Cookiecutter shark diel migration
    Depth and migration of cookiecutter sharks | Image credit: Johnson-Gould, J. (2011)

    Light in the dark: photophores and deception

    Cookiecutter sharks are not only adapted for darkness—they produce it. Embedded within their skin are photophores, specialized light-emitting organs that allow the shark to generate bioluminescence. Detailed anatomical and biochemical analyses show that these photophores are distributed across much of the ventral surface, creating a soft glow that closely matches downwelling light from the surface at night (Delroisse et al., 2014).

    This light is not decorative. It functions as counterillumination, a camouflage strategy common among midwater organisms, in which emitted light reduces the shark’s silhouette when viewed from below. Against the faint glow of the night surface, the shark effectively erases its outline. Only one area remains dark: the region beneath the jaw. That shadowed patch may act as a visual lure, resembling a small fish when seen from a distance—drawing larger predators close enough for the cookiecutter to strike (Delroisse et al., 2014).

    The photogenic skin of Isistius brasiliensis is also chemically complex. Enzymatic studies reveal multiple biochemical pathways involved in light production (bioluminescence), suggesting fine control over luminescence intensity and distribution (Delroisse et al., 2014). In the open ocean at night, where contrast matters more than size, this combination of light and shadow allows a small shark to manipulate perception—remaining unseen until it is already attached.

    This ability to move invisibly through the pelagic night helps explain both the cookiecutter shark’s success and its absence from human observation. Like its scars, its light is part of an ecology that works best when it goes unnoticed.

    image of cookiecutter shark photophores
    (A) Dorsal view of cookiecutter shark; (B) Dorsal view of cookiecutter shark’s photophores | Photo credit: Delroisse J, Duchatelet L, Flammang P and Mallefet J (2021)

    Do cookiecutter sharks occur off North Carolina?

    There are no records of resident cookiecutter sharks in nearshore North Carolina waters, and none would be expected. However, the western North Atlantic—including waters influenced by the Gulf Stream—falls well within the documented range of Isistius brasiliensis (Compagno, 1984).

    While the sharks themselves remain far offshore, the animals that pass our coast often arrive bearing quiet records of where they have already traveled—small, circular marks that hint at warm pelagic waters well beyond our horizon.

    Many species that migrate past North Carolina seasonally—swordfish, tunas, offshore dolphins, and large whales—spend portions of their annual cycle in oceanic regions where cookiecutter sharks are active. When those animals move northward or closer to the continental shelf, they may carry visible evidence of those offshore encounters.

    Scars as evidence: how cookiecutter sharks touch our region

    cookiecutter shark bites from fresh to healed
    Evidence of cookiecutter shark bites | Photo credit: Menezes, R., Marinho, J.P.D., de Mesquita, G.C. et al. (2022)

    Some of the clearest evidence for cookiecutter sharks in the Atlantic comes from the scars themselves. Circular crater wounds on swordfish have been used to infer the distribution and biogeography of Isistius brasiliensis in the North Atlantic (Muñoz-Chápuli et al., 1988). Similar bite marks have been documented on multiple tuna species, confirming repeated interactions between cookiecutter sharks and highly migratory pelagic fishes (Niella et al., 2018).

    Large whales tell the same story. Studies have documented characteristic cookiecutter scars across multiple whale species, often accumulated during time spent in warmer offshore waters and retained as animals migrate into higher latitudes (Best et al., 2016). In the Gulf of Mexico, cookiecutter bite wounds have been recorded on several cetacean species, reinforcing the consistency of this interaction across the western Atlantic (Grace et al., 2018).

    In this way, a scar becomes more than an injury; it functions as a trace of movement, carried northward by the same currents that shape our winter seas, like a passport stamp of their journey.

    What a cookiecutter scar looks like

    Cookiecutter scars are often described as “punched out.” In the scientific literature, they are characterized by:

    • Circular or oval crater-shaped wounds
    • Clean, well-defined edges
    • Relatively consistent size
    • Often multiple scars on a single individual

    When these features occur together—particularly on pelagic fishes or marine mammals—they are widely attributed to Isistius species (Best et al., 2016; Niella et al., 2018).

    cookiecutter shark bites on a great white shark
    A great white shark bears the marks of a cookiecutter shark – a fresh bite (upper image) and scarring from previous bite (lower image) | Photo credit: Mauricio Hoyos-Padilla et al. (2013)

    Closing: marks of a longer journey

    Cookiecutter sharks remind us that our coastal waters are shaped by lives lived far beyond the horizon. In winter, when migrations tighten along the Gulf Stream, animals pass our shore carrying the quiet evidence of where they have already been. Those circular scars are not just wounds; they are records—impressions left by warm nights, deep water, and encounters that happened far offshore.

    Long after the shark itself has disappeared into the pelagic dark, its mark remains. A small, precise circle becomes a trace of movement, a reminder that the animals we see here arrive with histories written on their bodies. In that way, cookiecutter scars function like a biological travel log—proof that our local waters are connected to distant places, and that the ocean keeps track of its travelers even when we do not.

    References

    Best, P. B., & Photopoulou, T. (2016). Identifying the “demon whale-biter”: Patterns of scarring on large whales attributed to a cookie-Cutter shark Isistius Sp. PLOS ONE, 11(4), e0152643. https://doi.org/10.1371/journal.pone.0152643

    Carlisle, A. B., Allan, E. A., Kim, S. L., Meyer, L., Port, J., Scherrer, S., & O’Sullivan, J. (2021). Integrating multiple chemical tracers to elucidate the diet and habitat of Cookiecutter sharks. Scientific Reports, 11(1). https://doi.org/10.1038/s41598-021-89903-z

    Compagno, L. J. (1984). FAO species catalogue, Vol. 4: Sharks of the world, Part 1 – Hexanchiformes to Lamniformes (125). FAO Fisheries Synopsis.

    Delroisse, J., Duchatelet, L., Flammang, P., & Mallefet, J. (2021). Photophore distribution and enzymatic diversity within the photogenic integument of the Cookie-Cutter shark Isistius brasiliensis (Chondrichthyes: Dalatiidae). Frontiers in Marine Science, 8. https://doi.org/10.3389/fmars.2021.627045

    Grace, M. A., Dias, L. A., Maze-Foley, K., Sinclair, C., Mullin, K. D., Garrison, L., & Noble, L. (2018). Cookiecutter shark bite wounds on cetaceans of the Gulf of Mexico. Aquatic Mammals, 43(5), 491-499. https://doi.org/10.1578/am.44.5.2018.491

    Muñoz-Chápuli, R., Salgado, J. C., & Serna, J. M. (1988). Biogeography of Isistius brasiliensis in the north-eastern Atlantic, inferred from crater wounds on swordfish (<i>Xiphias gladius</i>). Journal of the Marine Biological Association of the United Kingdom, 68(2), 315-321. https://doi.org/10.1017/s0025315400052218

    Niella, Y. V., Duarte, L. A., Bandeira, V. R., Crespo, O., Beare, D., & Hazin, F. H. (2018). Cookie‐Cutter shark Isistius spp. predation upon different tuna species from the south‐western Atlantic Ocean. Journal of Fish Biology, 92(4), 1082-1089. https://doi.org/10.1111/jfb.13569

    Papastamatiou, Y. P., Wetherbee, B. M., O’Sullivan, J., Goodmanlowe, G. D., & Lowe, C. G. (2010). Foraging ecology of Cookiecutter sharks (Isistius brasiliensis) on pelagic fishes in Hawaii, inferred from prey bite wounds. Environmental Biology of Fishes, 88(4), 361-368. https://doi.org/10.1007/s10641-010-9649-2