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Sharks of Onslow County

The Winter Guild: Nearshore Sharks and the Ecology of Cold Water

On a winter morning in Surf City, the beach feels emptied of its usual cast. Pelicans still cruise the shoreline in loose, patient lines, rising and settling with the wind. Gulls hover over seams in the water where green folds into brown. The tide sounds heavier now, denser, carrying cold through the shallows.

Along Topsail Island, the nearshore zone becomes a narrow corridor of motion and restraint. Waves collapse without urgency. The water clears between fronts. What summer spreads wide, winter compresses.

To most people, this looks like absence. The season reads as retreat.

But the coastal system has not gone dormant. It has been edited.

Cold water does not simply slow life along the coast; it reorganizes it. As the air cools, shallow waters lose heat first. Deeper layers follow. The sharp thermal steps of summer—warm surface, cool bottom—soften into sameness. What had been stacked becomes blended. Oceanographers describe this seasonal collapse as thermal and density homogenization (Cai et al., 2021), but on the shore it feels like weight: the water darker, heavier, less willing to give anything up.

This change reshapes everything that lives within it. Temperature governs metabolism. Light governs production. Density governs movement. Winter redraws those rules.

Predation does not vanish. It narrows.

Reading the Cold and Salt

Winter along the Carolina coast is defined less by dates than by gradients. Surface waters along the inner shelf commonly cool into the range of about 8–12 °C (46–54 °F), while deeper waters offshore remain slightly warmer under the influence of slope waters and the Gulf Stream (Atkinson et al., 1983; Cai et al., 2021; Rasmussen et al., 2005). The warm-bottom refuges of summer collapse. The mixed layer deepens. A single, colder column replaces the layered world of warm months.

Sea surface temperature (SST) range for Topsail Island, NC from 1981-2005. The thick yellow line shows average SST compared to 1984, while thin, black lines show extreme temperatures. | Photo credit: Surf-forecast.com, 2005
Sea surface temperature (SST) range for Topsail Island, NC from 1981-2005. The thick yellow line shows average SST compared to 1984, while thin, black lines show extreme temperatures. | Photo credit: Surf-forecast.com, 2005

Salinity follows a similar simplification. In winter, open shelf waters settle into a narrow band—typically around 32–35 parts per thousand (ppt), the same saltiness as the open Atlantic. Freshwater input diminishes, and stronger winds and tides smooth what summer once layered.

Average salinity utilizing historical ship and buoy data. Notice practical salinity is higher (red) along the North Carolina coastline. | Photo credit: World Ocean Atlas, 2009
Average salinity utilizing historical ship and buoy data. Notice practical salinity is higher (red) along the North Carolina coastline. | Photo credit: World Ocean Atlas, 2009

In summer, that chemistry fractures. Heavy rains, river discharge, and weak vertical mixing dilute nearshore and estuarine waters into the low 20s ppt or even the teens, sending plumes of brackish water outward from creek mouths and sounds (Singer et al., 1980). Onslow Bay becomes chemically patchworked: stratified sounds, plume-fed inlets, and salinity fronts that drift and reform with each tide.

Winter erases that mosaic. Only near inlets and estuary mouths do sharp gradients persist, briefly stacking fresher creek water over denser seawater before winds and tides flatten them again. Where summer offered a quilt of chemical habitats, winter replaces it with continuity.

Light changes too. Shorter days and deeper mixing reduce phytoplankton growth, pushing the productive layer below the surface and dimming the water’s green cast. Satellite and in situ records from the Mid-Atlantic shelf show winter as the seasonal low point for surface chlorophyll and primary productivity (Xu et al., 2011). The surface darkens. The food web thins from its base upward.

Winter does not remove life. It rearranges it.

Benthic invertebrates burrow or slow. Many fishes retreat or become lethargic. Bait compresses into fewer corridors—thermal seams, nearshore troughs, inlet mouths, shelf breaks—where temperature and oxygen remain tolerable. What summer scattered across marsh, creek, sound, and surf now funnels into lines.

This is what the filter does. It sheds surplus. It strips away species that require warmth, shallow stability, or dense prey. What remains are animals built to endure cold, exploit structure, or move precisely between systems.

Winter does not simplify the coast. It sharpens it.

3D perspective of coastline of Topsail Beach inner shoreface visualizes depth. | Photo credit: Greenhorn & O'Mara Consulting Engineers & Geodynamics, 2007, p. 221
3D perspective of coastline of Topsail Beach inner shoreface visualizes depth. | Photo credit: Greenhorn & O’Mara Consulting Engineers & Geodynamics, 2007, p. 221

The Inshore Winterer: Atlantic Spiny Dogfish

By midwinter, nearshore waters along this coast settle into a narrow thermal band—often between about 8 and 12 °C (46–54 °F) from surface to bottom (Atkinson et al., 1983; Cai et al., 2021). For many coastal fishes, that range marks the edge of activity. For Atlantic spiny dogfish (Squalus acanthias), it is home.

Across the North Atlantic, dogfish remain active in waters as cold as 4–6 °C (39–43 °F), with their highest densities often occurring well below the temperatures that drive other sharks away (Bangley & Rulifson, 2014; Sulikowski et al., 2010). Their physiology, growth patterns, and life history are tuned to persistence rather than speed, favoring endurance in lean systems over burst performance in rich ones (Tribuzio et al., 2010).

When winter flattens the water column into uniform cold, dogfish are not pushed to the margins of survival. They are moving within their preferred envelope.

Their bodies are built for this season. Unlike sharks bound to a narrow depth band, dogfish move freely through the water column—from the surface to depths approaching 200 meters—tracking temperature and prey through vertical space (Campana et al., 2009; Carlson et al., 2014; Sulikowski et al., 2010). In winter, when baitfish and invertebrates compress into fewer layers, that vertical freedom becomes a hunting advantage. A predator locked to one plane must wait. Dogfish can follow.

Nearshore waters and inlets become conveyor belts in winter. Tides concentrate prey flushed from estuaries. Cold fronts reorganize the column. What looks empty from the beach is often a thin band of movement just beyond the breakers. Dogfish occupy that band—persistent, economical, often in loose groups—feeding on schooling fishes and benthic prey even as energy margins tighten (Bangley & Rulifson, 2014).

Winter does not exclude them. It clears room for them.

The Atlantic spiny dogfish moves freely through the water column from the surface up to 200 meters. | Photo credit: ©Malcolm Francis
The Atlantic spiny dogfish moves freely through the water column from the surface up to 200 meters. | Photo credit: ©Malcolm Francis

The Threshold Species: Sandbar Sharks

Sandbar sharks (Carcharhinus plumbeus) read that same winter map very differently. In warm months, juveniles rely on shallow estuaries where bottom temperatures routinely exceed 15–18 °C (59–64 °F), conditions that accelerate growth, digestion, and survival (Bangley et al., 2018; Collatos, Abel & Martin, 2020). These flats become engines of development—wide, shallow spaces where warmth turns food into body.

By winter, those same bottoms cool into the low teens Celsius—often around 10–13 °C (50–55 °F) and sometimes lower. The estuary does not become lethal. It becomes unprofitable. Feeding no longer offsets the energetic cost of movement and digestion in cold water, particularly for juveniles still building mass.

Unlike dogfish, sandbar sharks cannot remain inside a cold system and adapt to its structure. Their bodies and life histories are tuned to warm, shallow stability. Their performance drops rapidly as temperature declines; muscle efficiency, digestion, and growth all slow (Crear et al., 2019). When that stability collapses, they respond laterally rather than vertically—sliding down the coast or into slightly deeper nearshore waters where bottom temperatures remain marginally warmer (Bangley et al., 2018).

Where dogfish remain and work winter’s compression, sandbars leave it.

They are still part of the region, but they are absent from the nearshore corridor. They become threshold species—present in the seasonal arc, absent from the winter system itself. The estuary no longer belongs to them.

Sandbar sharks will move to warmer water in winter and will move to deeper offshore waters or move southward down the coast. | Photo credit: (c) The Wet Lens, 2023
Sandbar sharks will move to warmer water in winter and will move to deeper offshore waters or move southward down the coast. | Photo credit: (c) The Wet Lens, 2023

The Offshore Presence: Dusky Sharks

Dusky sharks (Carcharhinus obscurus) follow a third geometry. They tolerate cool water, but within a narrower band than many coastal sharks—most often occupying waters between roughly 10 and 20 °C (50–68 °F) (Bangley et al., 2020; Manz et al., 2025). When nearshore temperatures along this coast fall into that range, duskies can be present. When they rise beyond it in spring and summer, they are gone.

Their winter preference therefore lies not in the compressed nearshore column, but along offshore corridors where temperature is steadier and remains within that narrow envelope. Shelf and slope waters influenced by the Gulf Stream often stay buffered within those bounds even as inshore waters swing widely (Atkinson et al., 1983; Rasmussen et al., 2005).

Dusky sharks do not attempt to work winter’s compression. They choose stability instead. Rather than hunting within a narrowed corridor, they reposition along thermally buffered routes where cold arrives slowly and predictably.

From land, this reads as vacancy. The surf appears emptied. Yet beyond the bar, duskies remain active in a parallel winter economy—tracking prey along shelf edges and slope corridors invisible from shore.

They have not disappeared. They have changed address.

Dusky sharks prefer cooler temperature waters and may be present in our nearshore waters. However, when waters warm beyond 20 °C (68 °F), they will move to cooler waters. | Photo credit: jmartincrossley, iNaturalist, 2026
Dusky sharks prefer cooler temperature waters and may be present in our nearshore waters. However, when waters warm beyond 20 °C (68 °F), they will move to cooler waters. | Photo credit: jmartincrossley, iNaturalist, 2026

Winter as an Ecological Filter

By February, the coast has shed its surplus.

The fish that needed warmth are gone. The invertebrates that depended on light have slowed or buried. What remains are species built to move through cold, to wait, or to follow structure instead of abundance.

Winter filters by physics first.

A deep mixed layer removes warm-bottom refuges (Cai et al., 2021). Bottom-water intrusions in Onslow Bay and adjacent shelf waters restructure the vertical habitat, replacing summer’s layered gradients with cold continuity (Hofmann et al., 1981). Uniform salinity simplifies the chemical landscape. Reduced light and productivity shrink the food web’s base (Xu et al., 2011). Currents sharpen boundaries between inshore and offshore waters, and periodic Gulf Stream intrusions create moving seams of heat and prey (Atkinson et al., 1983; Rasmussen et al., 2005).

These constraints become biological.

Prey compress. Movement costs rise. Energy budgets tighten. Species that require constant warmth, shallow stability, or dense forage are excluded. Those that remain are specialists: animals that tolerate cold, exploit vertical structure, or reposition with precision.

Dogfish persist because they can work the layered winter column, remaining inside nearshore waters and inlets even as surface and bottom temperatures converge. Sandbar sharks withdraw from estuaries and shallow flats, shifting down the coast or into slightly deeper nearshore habitats where bottom temperatures remain metabolically tolerable. Dusky sharks relocate more completely, leaving the coastal corridor for offshore shelf and slope waters where Gulf Stream influence preserves thermal stability and prey remains distributed.

Each species reads the same season and answers it differently—not by disappearance, but by repositioning within a changing map.

Winter does not erase complexity. It concentrates it.

Meteorological seasons are based upon the annual temperature cycle and differ from the astronomical seasons based upon the position of the sun relative to the Earth. The meteorological seasons help scientists track climate and weather changes. | Photo credit: NOAA, 2024
Meteorological seasons are based upon the annual temperature cycle and differ from the astronomical seasons based upon the position of the sun relative to the Earth. The meteorological seasons help scientists track climate and weather changes. | Photo credit: NOAA, 2024

A Season That Is Beginning to Shift

The cues that drive migration—photoperiod, temperature thresholds, energetic margins—are no longer fixed. Recent models suggest that warming oceans are already altering how and when coastal sharks move, stretching winter windows and delaying departures (Manz et al., 2025).

This does not announce collapse. It signals reorganization.

From the beach, the change may remain imperceptible. The surf will still look calm. Pelicans will still cruise. The marsh will still pale. But beneath that surface, the system will continue to read its invisible clocks.

Winter along Surf City and Topsail Island is not an end. It is a narrowing—a season where cold, salt, light, and current decide who remains.

They are still here. They have simply become harder to see.

References

Atkinson, L. P., Lee, T. N., Blanton, J. O., & Chandler, W. S. (1983). Climatology of the southeastern United States continental shelf waters. Journal of Geophysical Research: Oceans, 88(C8), 4705-4718. https://doi.org/10.1029/jc088ic08p04705

Bangley, C. W., Curtis, T. H., Secor, D. H., Latour, R. J., & Ogburn, M. B. (2020). Identifying important juvenile dusky shark habitat in the Northwest Atlantic ocean using acoustic telemetry and spatial modeling. Marine and Coastal Fisheries, 12(5), 348-363. https://doi.org/10.1002/mcf2.10120

Bangley, C. W., Paramore, L., Dedman, S., & Rulifson, R. A. (2018). Delineation and mapping of coastal shark habitat within a shallow lagoonal Estuary. PLOS ONE, 13(4), e0195221. https://doi.org/10.1371/journal.pone.0195221

Bangley, C. W., & Rulifson, R. A. (2014). Feeding habits, daily ration, and potential predatory impact of mature female spiny dogfish in North Carolina coastal waters. North American Journal of Fisheries Management, 34(3), 668-677. https://doi.org/10.1080/02755947.2014.902410

Cai, C., Kwon, Y., Chen, Z., & Fratantoni, P. (2021). Mixed layer depth climatology over the Northeast U.S. continental shelf (1993–2018). Continental Shelf Research, 231, 104611. https://doi.org/10.1016/j.csr.2021.104611

Campana, S. E., Jamie, A., & Gibson, F. (2008). Stock structure, life history, fishery and abundance indices for spiny dogfish (Squalus Acanthias) in Atlantic Canada (2007/089). Canadian Science Advisory Secretariat. https://www.researchgate.net/publication/268389393_Stock_Structure_Life_History_Fishery_and_Abundance_Indices_for_Spiny_Dogfish_Squalus_acanthias_in_Atlantic_Canada

Carlson, A. E., Hoffmayer, E. R., Tribuzio, C. A., & Sulikowski, J. A. (2014). The use of satellite tags to redefine movement patterns of spiny dogfish (Squalus acanthias) along the U.S. East Coast: Implications for fisheries management. PLoS ONE, 9(7), e103384. https://doi.org/10.1371/journal.pone.0103384

Collatos, C., Abel, D. C., & Martin, K. L. (2020). Seasonal occurrence, relative abundance, and migratory movements of juvenile sandbar sharks, Carcharhinus plumbeus, in Winyah Bay, South Carolina. Environmental Biology of Fishes, 103(7), 859-873. https://doi.org/10.1007/s10641-020-00989-2

Crear, D. P., Brill, R. W., Bushnell, P. G., Latour, R. J., Schweiterman, G. D., Steffen, R. M., & Weng, K. C. (2019). The impacts of warming and hypoxia on the performance of an obligate ram ventilator. Conservation Physiology, 7(1). https://doi.org/10.1093/conphys/coz026

Greenhorn & O’Mara Consulting Engineers, & Geodynamics. (2007). High-Resolution 3D Bathymetric Assessment of Potential Hard Bottom Habitats: Topsail Island, Surf City and North Topsail Island, NC (Project No. DACW54-02-D-0006, Delivery Order 0035 Modification 01 Nearshore Hardbottom Sidescan Survey for Multibeam Data Collections Topsail Island, NC G&O Project Number 146046.T35.6481.GEO). https://www.saw.usace.army.mil/Portals/59/docs/coastal_storm_damage_reduction/SCNTB/R%20-%20Hard%20Bottom%20Survey%20Reports.pdf

Hofmann, E. E., Pietrafesa, L. J., & Atkinson, L. P. (1981). A bottom water intrusion in Onslow Bay, North Carolina. Deep Sea Research Part A. Oceanographic Research Papers, 28(4), 329-345. https://doi.org/10.1016/0198-0149(81)90003-0

Manz, M. H., Shipley, O. N., Cerrato, R. M., Hueter, R. E., Newton, A. L., Tyminski, J. P., Franks, B. R., Curtis, T. H., Fischer, C., Zacharias, J. P., Scott, C., Dunton, K. J., Kneebone, J., Peterson, B. J., Scannell, B. J., Dodd, J. F., & Frisk, M. G. (2025). Predictions of southern migration timing in coastal sharks under future ocean warming. Conservation Biology, 39(6). https://doi.org/10.1111/cobi.70080

NASA Salinity. (2011, October 20). Average Salinity From Historical Ship and Buoy Data. https://salinity.oceansciences.org/gallery-images-more.htm?id=10

Rasmussen, L. L., Gawarkiewicz, G., Owens, W. B., & Lozier, M. S. (2005). Slope water, Gulf Stream, and seasonal influences on southern Mid‐Atlantic bight circulation during the fall‐winter transition. Journal of Geophysical Research: Oceans, 110(C2). https://doi.org/10.1029/2004jc002311

Singer, J. J., Atkinson, L. P., & Pietrafesa, L. J. (1980). Summertime advection of low salinity surface waters into Onslow Bay. Estuarine and Coastal Marine Science, 11(1), 73-82. https://doi.org/10.1016/s0302-3524(80)80030-2

Sulikowski, J., Galuardi, B., Bubley, W., Furey, N., Driggers, W., Ingram, G., & Tsang, P. (2010). Use of satellite tags to reveal the movements of spiny dogfish Squalus acanthias in the western North Atlantic Ocean. Marine Ecology Progress Series, 418, 249-254. https://doi.org/10.3354/meps08821

Surf-forecast.com. (2005). Topsail island water temperature (Sea) and wetsuit guide (Carolina north, USA). https://www.surf-forecast.com/breaks/Topsail-Island/seatemp

Tribuzio, C. A., Kruse, G. H., & Fujioka, J. T. (2010). Age and growth of spiny dogfish (Squalus acanthias) in the Gulf of Alaska: analysis of alternative growth models ( Fishery Bulletin(Vol. 108, Issue 2)). National Marine Fisheries Service. https://go.gale.com/ps/i.do?id=GALE%7CA227944663&sid=googleScholar&v=2.1&it=r&linkaccess=abs&issn=00900656&p=AONE&sw=w&userGroupName=anon%7E4fe11d55&aty=open-web-entry

Xiu, Y., Chant, R., Gong, D., Castelao, R., Glenn, S., & Schofield, O. (2011). Seasonal variability of chlorophyll a in the Mid-Atlantic Bight. Continental Shelf Research, 31(16), 1640-1650. https://doi.org/10.1016/j.csr.2011.05.019

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