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Shark Sleigh Bells: How Sharks Track Vibrations in the Winter Sea

Winter’s Quiet Chorus

December hushes the coastline of Onslow County. The marshgrass stiffens in the cold, the surf stills between storms, and the New River Inlet carries the metallic stillness of early winter. Yet beneath that calm, the water hums with motion — tiny pulses, ripples, and vibrations that weave a hidden holiday soundtrack, a kind of underwater sleigh bells rung in pressure waves.

Sharks, lingering along the nearshore troughs or cruising the outer edge of the estuary, sense these disturbances with remarkable clarity. Every mullet tail-beat, crab scuttle, and sediment shift radiates through the water as a low-frequency pressure wave. In the quiet of December, these signals travel farther and cleaner, strengthened by winter’s denser water, slower prey, and reduced turbidity (Mickle & Higgs, 2021; Mogdans, 2019).

To sharks, these vibrations form a map, a three-dimensional winter soundscape that reveals direction, distance, and urgency (Montgomery, Baker & Carton, 2000; Montgomery et al., 2000). And layered beneath these hydrodynamic cues, the faint electric fields produced by the heartbeat and muscle activity of nearby prey glow through the water, detectable at nanovolt precision (Anderson et al., 2017; England et al., 2021).

This “music” is not metaphor — it is the sensory world sharks inhabit, sharpened by the very conditions winter imposes.

The Winter Sea as a Soundscape

Illustration showing how different animals create underwater vibrations detectable by sharks. A school of fish at the top produces wide, rolling displacement waves. A crab on the sandy seafloor generates small, intermittent pulse rings. Two individual fish create subtle fin-flick ripple patterns. Concentric circles radiate from each animal to visually represent hydrodynamic cues in the water.
Sharks detect a wide range of underwater vibrations—from the rolling displacement waves of schooling fish to the intermittent pulses of crabs and the subtle fin flicks of solitary prey—using their highly sensitive mechanosensory systems.

Cold water shifts the physics of survival. As temperatures fall, prey metabolism slows, creating weaker and more irregular movement patterns — the exact low-frequency signatures sharks detect most easily (Sisneros & Rogers, 2016). Reduced plankton and sediment yield a clearer path for particle motion, allowing hydrodynamic cues to propagate farther through the winter water column (Mogdans, 2019).

This turns the estuary into a rich field of vibrations. Fish schooling tightly create rolling displacement waves. Crabs shifting beneath the sand produce intermittent pulses. Even subtle fin flicks produce particle motion detectable by sharks’ sensory systems (Maruska, 2001).

Winter looks barren to us.
To sharks, it resonates.

Hydrodynamic “Bells”: The Lateral Line

A scientific-style illustration explaining how a shark’s lateral line detects underwater vibrations. A sandbar shark is shown with a highlighted lateral line running along its body and head. Concentric rings radiate from a struggling fish, a crustacean on the seafloor, and a distant object to demonstrate low-frequency hydrodynamic signals. Icons represent cold water, low light, prey movement, and inlet geometry as factors that enhance vibration transmission in winter. Text describes neuromasts encoding direction and amplitude to create a spatial map of nearby activity.
Sharks use their lateral line to “feel” tiny vibrations in the water. Winter makes these signals even easier to detect, helping sharks follow the movement of fish, crabs, and other prey in low-light conditions.

The shark’s lateral line is a mechanosensory canal system tuned to detect water displacement in the exact frequency range produced by struggling fish and crustaceans (Montgomery, Baker & Carton, 2000). Neuromasts within the canal encode both direction and amplitude, transforming low-frequency motion into a spatial map of nearby activity (Mogdans, 2019).

In December, this system excels:

  • cold water enhances transmission of pressure waves,
  • prey move more predictably and more weakly,
  • low-light conditions reduce visual noise,
  • and inlet geometry funnels vibrations along natural corridors.

Even acoustic cues — particle motion at frequencies under ~300 Hz — become part of this integration. Sharks are most sensitive to these low-frequency bands, enabling discrimination of movement types in murky or dark winter water (Poppelier et al., 2022).

To a shark, each pulse is information.
Each ripple is direction.
Each vibration is a bell rung underwater.

Watch how sharks use their lateral line system to sense ripples and vibrations long before they see their prey. | Video courtesy of National Aquarium – “Sharks Lateral Line”

Closer Than Sight: The Ampullae of Lorenzini

When a shark closes the final distance, tracking transitions from vibration to electricity. The Ampullae of Lorenzini detect microvolt-scale electric fields emitted by the body of every living animal. Sensitivity thresholds fall into the tens of nanovolts per centimeter — among the most refined biological detection limits known (Anderson et al., 2017; Newton, Gill & Kajiura, 2019; England et al., 2021).

Electroreception enables sharks to:

  • locate prey buried beneath sand,
  • perceive fish hidden in silt clouds,
  • detect immobile or slow-moving animals,
  • and navigate complex, low-light environments.

Classic electroreception work demonstrated these capacities decades ago, and modern experimental studies in hammerheads confirm high-resolution electro-sensitivity during close-range hunting (Kajiura & Holland, 2002; Kalmijn, 2000).

In winter, when storms churn the sediment and twilight comes early, this sense becomes even more essential.

Sharks do not need light — they follow electricity.

Video courtesy of PBS Deep Look, illustrating how sharks use electroreception to locate prey invisible to sight or sound.

A December Hunt at the New River Mouth

Illustration of a juvenile Atlantic sharpnose shark approaching a partially buried mullet in shallow winter water. Orange concentric lines show the mullet’s electric field and the shark’s detection of hydrodynamic and electrical cues through its lateral line and Ampullae of Lorenzini.
A juvenile Atlantic sharpnose shark follows the faint hydrodynamic pulse of a cold-slowed mullet, then locks onto its electric field—an underwater hunt guided by vibration and microvolts.

Picture a December evening at the New River Inlet. The ebb tide pulls cold water from the sound toward the ocean. A juvenile Atlantic sharpnose shark glides along a shallow bar, guided not by sight, but by the underwater vibrations pulsing through its lateral line.

A faint, uneven pressure wave reaches the shark — the hydrodynamic signature of a mullet slowed by the cold (Montgomery et al., 2000). The shark turns. Another pulse follows, the rhythm revealing both direction and weakness.

Within a few body lengths, electric cues rise above the hydrodynamic noise. The Ampullae of Lorenzini detect microvolt-scale oscillations from the mullet’s buried body (Newton, Gill & Kajiura, 2019; England et al., 2021). One quick strike completes the hunt.

This is winter’s choreography:
vibrations at a distance,
electricity up close,
all woven seamlessly through still December water.

The Importance of Winter Hunting

four-panel educational graphic titled “Winter Survival: How Sharks Thrive When Other Animals Slow Down.” The top panels show a shark pursuing a slow-moving fish labeled “Winter Energy Reserves” and a shark navigating an inlet with arrows labeled “Predictable Movement Corridors.” The bottom panels show a shark approaching a weakened fish with vibration rings labeled “Removing Weakened Individuals” and a shark outlined by sensory icons—spiral wave, lightning bolt, and low-light symbol—labeled “Low Visibility Navigation.” The artwork illustrates how sharks use sensory advantages to hunt effectively during winter.
Even as the season quiets the coast, sharks thrive—reading vibrations, following winter corridors, finding weakened prey, and navigating the dim water with senses far beyond our own.

Although prey slow in winter, sharks must continue to feed. Their dual sensory systems allow efficient predation in the season that challenges most marine animals. These abilities help sharks:

  • build winter energy reserves,
  • exploit predictable movement corridors,
  • maintain population stability by removing weakened individuals (Tricas & McCosker, 1984),
  • and navigate cold, low-visibility environments effectively (Mickle & Higgs, 2021).

Even as water temperatures drop, species like Atlantic sharpnose sharks, bonnetheads, and offshore Atlantic spiny dogfish remain active, relying heavily on the interplay of hydrodynamic and electroreceptive cues (Maruska, 2001).

Winter is not lifeless.
It is a sensory masterclass.

Bells That Never Stop Ringing

While we celebrate the holidays with sleigh bells, carols, and glowing lights, the Atlantic hums with its own winter rhythms. Sharks navigate December through vibrations, particle motion, and faint electrical fields — signals older than any tradition and tuned to the pulse of life beneath the cold.

Their bells are not made of metal.
They are made of motion.
Of electricity.
Of the quiet echoes of survival beneath the tide. These are the Shark Sleigh Bells, ringing softly beneath Onslow County’s winter waters.

References

Anderson, J. M., Clegg, T. M., Véras, L. V., & Holland, K. N. (2017). Insight into shark magnetic field perception from empirical observations. Scientific Reports, 7(1). https://doi.org/10.1038/s41598-017-11459-8

England, S. J., & Robert, D. (2021). The ecology of electricity and electroreception. Biological Reviews, 97(1), 383-413. https://doi.org/10.1111/brv.12804

Kajiura, S. M., & Holland, K. N. (2002). Electroreception in juvenile scalloped hammerhead and sandbar sharks. Journal of Experimental Biology, 205(23), 3609-3621. https://doi.org/10.1242/jeb.205.23.3609

Kalmijn, A. J. (2000). Detection and processing of electromagnetic and near–field acoustic signals in elasmobranch fishes. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 355(1401), 1135-1141. https://doi.org/10.1098/rstb.2000.0654

Maruska, K. P. (2001). Morphology of the Mechanosensory lateral line system in elasmobranch fishes: Ecological and behavioral considerations. Environmental Biology of Fishes, 60(1-3), 47-75. https://doi.org/10.1023/a:1007647924559

Mickle, M. F., & Higgs, D. M. (2021). Towards a new understanding of elasmobranch hearing. Marine Biology, 169(1). https://doi.org/10.1007/s00227-021-03996-8

Mogdans, J. (2019). Sensory ecology of The Fish lateral‐line system: Morphological and physiological adaptations for the perception of hydrodynamic stimuli. Journal of Fish Biology, 95(1), 53-72. https://doi.org/10.1111/jfb.13966

Montgomery, J., Carton, G., Voigt, R., Baker, C., & Diebel, C. (2000). Sensory processing of water currents by fishes. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 355(1401), 1325-1327. https://doi.org/10.1098/rstb.2000.0693

Montgomery, J. C., Baker, C. F., & Carton, A. G. (1997). The lateral line can mediate rheotaxis in fish. Nature, 389(6654), 960-963. https://doi.org/10.1038/40135

Newton, K. C., Gill, A. B., & Kajiura, S. M. (2019). Electroreception in marine fishes: Chondrichthyans. Journal of Fish Biology, 95(1), 135-154. https://doi.org/10.1111/jfb.14068

Poppelier, T., Bonsberger, J., Berkhout, B. W., Pollmanns, R., & Schluessel, V. (2022). Acoustic discrimination in the grey bamboo shark Chiloscyllium griseum. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-10257-1

Tricas, T. C., & McCosker, J. E. (1984). Predatory behavior of the white shark (Carcharodon carcharias) and other large sharks. Proceedings of the California Academy of Sciences, 43(14), 221-238. https://ia801302.us.archive.org/16/items/biostor-78396/biostor-78396.pdf 

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