Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Ecosystem engineering creates a direct nutritional link between 600-m deep cold-water coral mounds and surface productivity


Cold-water corals (CWCs) form large mounds on the seafloor that are hotspots of biodiversity in the deep sea, but it remains enigmatic how CWCs can thrive in this food-limited environment. Here, we infer from model simulations that the interaction between tidal currents and CWC-formed mounds induces downwelling events of surface water that brings organic matter to 600-m deep CWCs. This positive feedback between CWC growth on carbonate mounds and enhanced food supply is essential for their sustenance in the deep sea and represents an example of ecosystem engineering of unparalleled magnitude. This ’topographically-enhanced carbon pump’ leaks organic matter that settles at greater depths. The ubiquitous presence of biogenic and geological topographies along ocean margins suggests that carbon sequestration through this pump is of global importance. These results indicate that enhanced stratification and lower surface productivity, both expected consequences of climate change, may negatively impact the energy balance of CWCs.


Cold-water corals (CWC) are ecosystem engineers building extensive reefs that are habitat for a diverse fauna, such as sponges, crinoids and fish, making them hotspots of biodiversity1 and significant sinks of organic matter2,3 in the deep sea. Food limitation exerts a well-known control on biological activity in the deep sea, as the organic matter is produced in the sunlit surface ocean and rapidly degrades during the 100 s to 1,000 s of meters transit to the seafloor4. It is paradigmatic how diverse and productive CWCs can thrive in this resource-limited environment. A better understanding of how CWCs meet their nutritional demands is critically needed to assess how they will cope with climate-induced shifts in primary production5 and reduced water column mixing6. Moreover, it is increasingly clear that food availability is a key factor determining the sensitivity of CWCs to ocean acidification7,8.

Scleractinian CWCs form bottom topographies that are tens to hundreds meters high over thousands to millions of years9. The global distribution of CWCs renders carbonate mound and reef structures prominent topographic features of the seafloor along continental margins (Fig. 1). Recent studies in Scotland and Norway have suggested that the interaction of tidal currents with CWC reefs induces downwelling of surface water10,11,12 due to the formation of internal waves or hydraulic jumps10,12. As CWCs themselves form prominent topographies on the seafloor and these topographies induce downwelling of surface water, two intriguing questions naturally arise. Is there a positive feedback between CWC growth on carbonate mounds and food supply from the surface ocean? And, what are the implications for organic matter sequestration to the deep ocean?

Figure 1

Global map with occurrences (white dots) of Scleractinian cold-water corals57 (data available at

Red boxes indicate known locations along the continental shelves where Lophelia pertusa has shaped the seafloor topography into (A) a coral province of 20–40 m high in the Gulf of Mexico58, (B) coral ridges of up to 20 m high in Florida Strait59, (C) elongated mound clusters with the largest mounds reaching a height of 100 m off the coast of Mauritania60, (D) numerous and large carbonate mounds of up to 300 m high along the Irish margin16, (E) elongated CWC reefs, mostly between 10 and 15 m high, all along the Norwegian shelf3,31 and (F) up to 25-m high coral banks in the Mediterranean Sea61. Figure and basemap created with the R-package plot3D, version 1.1

In this study, we identify pathways of organic matter supply to 600-m deep CWCs along Rockall Bank (NE Atlantic) and provide evidence for a positive feedback between organic matter supply and CWC growth. Rockall Bank is rich in CWCs and represents a perfect study arena, because strongly contrasting CWC growth forms are found here (Fig. 2). On the eastern part, CWCs are predominantly found on the shelf-break ridge at 400 to 500 m water depth13,14 (Fig. 2). Just tens of kilometres to the west, the Logachev Mounds are found, a conspicuous CWC mound cluster of several kilometres long and up to 380 m high at a water depth of 600 to 1000 m 15,16. A coupled model was used to infer the organic matter supply pathways for the two contrasting CWC-rich regions at Rockall Bank (Methods). A 3D-hydrodynamic model17 is used to identify the frequency and intensity of downwelling events above the CWC mounds and the shelf break ridge. These hydrodynamic simulations were used to model organic matter dynamics in the water column. CWC uptake of suspended organic matter was imposed by combining their metabolic requirements2,3 with their occurrences based on a regional habitat suitability model14. We also quantitatively determine how the presence of CWC mounds influences organic carbon sequestration in the deep sea. The results of our modelling approach will be presented first, followed by the implications of our findings.

Figure 2

The modelled area of Rockall Bank with the two contrasting CWC growth forms: CWC growth on mounds (transected by the left line) and CWC growth on a ridge (transected by the right line).

The dimension of the area is 90 km (longitude) × 60 km (latitude) × 2.4 km (depth). Scale bar indicates depth of the seafloor. White dots indicate the predicted CWC occurrences from the habitat suitability model (see Methods). Inset figure shows the location of Rockall Bank along the Irish margin. Figure created with the R-package plot3D, version 1.1

Results and Discussion

Cold-water coral mounds induce up- and downwelling events

A 3D-hydrodynamic model generated flow fields along the eastern Rockall Bank (NE Atlantic Ocean) shelf break17 (Methods). The model domain covers an area (60 × 90 km) of Rockall Bank and extends from the shallow bank (200 m) down into the deep Rockall Trough (2000 m) (Fig. 2). We focus on two depth-transects within this model domain, one superimposed on the shelf-break ridge and another on the Logachev mound cluster (Fig. 2).

The monthly-averaged residual currents, calculated from the hydrodynamic model output, show that surface water enters the region primarily from the southeast, roughly perpendicular to the continental slope, and deflects southwest to Logachev mounds and northeast along the shelf break (Supplementary Figure 1). The residual near-bottom currents are heterogeneous and substantially stronger (up to >0.4 m s−1 in the Logachev mound province and <0.25 m s−1 on the ridge) than the surface currents and are directed southwest (Supplementary Figure 1).

Superimposed on these long-term residual currents however, are localised up- and downwelling events that show up in time series of vertical velocities (Fig. 3A–D, Supplementary Movie 1). While the average vertical current speed is between 0.002 and 0.004 m s−1, the maximum vertical up- and downwelling currents in the water column above the Logachev mounds reach peak values of up to 0.15 and 0.28 m s−1, respectively (Fig. 4A), whereas vertical current velocities are substantially weaker above the CWC on the coral ridge (Fig. 4B). The frequency of these events is however comparable in both areas and are driven by the tidal cycle (Fig. 4).

Figure 3

Model output of vertical current velocities (A–D) and organic matter concentration in the water column (E–H) along the coral mound (A,B,E,F) and coral ridge transect (C,D,G,H) during neap and spring tide.

Figure 4

Maximum up- (in red) and downwelling (in blue) current velocities (m s−1) occurring simultaneously in the model simulations above the coral mound region (A) and coral ridge region (B).

Stratified tidal flow over finite-amplitude topography can generate a multitude of disturbances in the flow and water-column stratification, including internal waves and upwelling or downwelling18,19. The initial response of tidal flow over a sill or bank, such as the large mounds of the Logachev Mound cluster, is a stationary lee wave adding a vertical component to the stratified flow and a downstream depression of isopycnals19. At the turn of tide the flow slackens and the lee wave can propagate upstream as a non-linear internal tidal bore or true internal hydraulic jump20. Recent studies identified tidally driven non-linear hydraulic control of flow over an abrupt topography as the major driver for rapid downwelling and vertical mixing at shallow CWC reefs10,12 and within the Logachev Mound province21, which may intensify in areas of strong depth variations and during periods of strongly amplified flow such as the spring/neap tidal cycle (Fig. 3, refs 12 and 21).

A topographically-enhanced organic matter pump

The flow fields of the hydrodynamic model are used to force a biogeochemical reaction-transport model, in which organic matter, produced in the photic zone, is subjected to passive sinking, hydrodynamical transport and biological degradation (see Methods). In the model, organic matter refers to a mixture of suspended sources (e.g. dissolved organic matter, bacteria, marine snow and small zooplankton) that are transported largely by hydrodynamics. Lophelia pertusa, together with other filter feeders in the reef community, is an opportunistic feeder that can feed on a range of organic matter sources22. Hence, this coupled hydrodynamic-biogeochemical model takes suspended organic matter as a non-conservative tracer to reconstruct organic food supply to the CWC-rich regions.

Model simulations reveal clearly contrasting transport mechanisms between both regions (Fig. 3 and the Supplementary Movie showing vertical current velocities and organic matter concentrations during the entire simulation period at 6 hour resolution).

The downwelling intensity above the mounds is relatively low at neap tide (Figs 3a and 4a) leaving the deep water-column poor in organic matter (Fig. 3E). During spring tide however, up- and downwelling currents intensify (Fig. 3B) resulting in organic matter plumes that are directed from the surface ocean towards the CWC-rich Logachev mounds (Fig. 3F). This localised downwelling occurs repeatedly during the lunar tidal cycle, but strongest downwelling events are observed during spring tide (Supplementary Movie). Towards the end of the lunar tidal cycle, vertical currents weaken and the deep water becomes more oligotrophic again (Supplementary Movie). From these simulations, it is clear that food supply is mainly sustained through vertical downwelling events that establish a direct link between 600-m deep cold-water coral mounds and surface productivity.

Along the shelf break ridge, the CWCs receive organic matter through a different transport mechanism (Fig. 3G,H). Vertical up- and downwelling is also observed above the ridge, but the intensity is lower (Fig. 3C,D) and does not generate directed organic matter plumes as found for the CWC mounds (Fig. 3G,H). Instead, there is retention of organic matter-rich waters above the shallow Rockall Bank that occasionally spills over the ridge down the slope (Fig. 3H). Hence, the dominant transport mechanism of organic matter to the CWCs on the shelf ridge appears to be downslope transport.

Organic matter distribution and sequestration

The high mineralization rates of CWC reef communities suggests that a local ‘focussing’ of organic matter onto these ecosystems must occur, which potentially lowers the availability of organic matter for the surrounding seafloor3. We evaluated this hypothesis quantitatively by plotting the modelled organic matter deposition against water depth across the model domain (Fig. 5A). The organic matter deposition on the CWCs on the mounds and ridge was elevated with a factor 5 to 10 as compared to the off-reef seafloor at similar water depth (Fig. 5A). A comparison of these initial model results with a model simulation in which the filtration activity of CWC was toggled off shows that this separation between organic matter deposition of CWCs versus the off-reef seafloor vanishes (Fig. 5B). Hence, the filtration activity of CWCs results in a ‘focussing’ of organic matter onto the CWCs at the expense of deposition on the off-reef seafloor at comparable water depth.

Figure 5

(A) Modelled organic matter deposition versus water depth in the various habitats within the model domain, (B) organic matter deposition versus water depth in absence of CWC filtration activity and (C) organic matter deposition versus water depth in the absence of hydrodynamics.

The interaction of CWC mounds and the shelf ridge supplies food to the CWCs, but this ‘topographically-enhanced pump’ may also enhance the sequestration of organic matter to the deep sea. To isolate the importance of hydrodynamic transport for the organic matter sequestration within the model domain, we ran a simulation in which organic matter was subjected only to passive sinking, biological degradation and CWC filtration activity. Interestingly, the organic carbon deposition beyond 1200 m water depth is up to an order of magnitude lower in the model simulations that lack hydrodynamics (Fig. 5C). This implies that part of the organic matter that is transported downward due to the topographically-enhanced pump ‘leaks’ away and settles on the seafloor at greater depths. Hence, the topographically-enhanced pump acts as a conduit of organic matter supply to the deeper seafloor.

Another striking feature that becomes clear from the model run in which the hydrodynamics were toggled off (Fig. 5C) is that organic matter deposition by mere passive sinking are grossly insufficient to sustain the high mineralization activity of CWC (measured to be between 8 to 88 mmol C m−2 d−12,3,23,24). While it is well-established that cold-water corals occur at locations with elevated current velocities, internal waves or turbulent mixing10,16,17,25,26, our model results provide direct evidence that hydrodynamic forcing is essential to sustain the metabolic activity of CWCs in the deep sea.

Implications and outlook

A fundamental question in oceanography is how CWCs can thrive in the food-limited deep ocean. The dominant view on this paradigm is described by the so-called ‘environmental control theory’27, which assumes that environmental factors control the distribution of CWCs. Key elements of this theory are that CWCs are found in regions with a relatively high surface productivity7 and enhanced hydrodynamic energy26, including high bottom currents16, retention within Taylor columns28,29 and breaking internal waves16,30. These factors ensure a sufficient supply of surface-derived organic matter to the filter-feeding CWCs9,31 and explain CWC occurrences in for example submarine canyons32 and sills11. Abiotic variables such as seawater density33, temperature25 and aragonite saturation state34 may further narrow down the suitable habitat of CWCs. Here we show that the seafloor topography that is created by the CWCs leads to a preferential focussing of organic matter towards these ecological hotspots. This focussing implies a positive feedback between CWC growth and food supply. Hence, rather that being under mere environmental control, CWCs modify their environment through mound formation, whereby food supply is stimulated. This positive feedback is a remarkable example of large-scale and long-term ecosystem engineering (sensu35). Hence, a more appropriate term to coin the factors that control CWC distribution would be the ‘ecosystem engineer control theory’.

It is challenging though to extrapolate from this single case study and assess whether this transport mechanism is important for the CWC reefs around the globe (Fig. 1) or other benthic ecosystems that are associated with seafloor topographies. However, it is well established that topographic rises, of both biogenic and geological origin, are ubiquitously present on the ocean floor36, which suggests that organic matter sequestration to the deep sea through a topographically-induced carbon pump could be of global importance. Indeed, predictions of the downward organic matter flux in the water column based on sinking, turbulent mixing and degradation of organic particles, i.e. the canonical Martin formula, often strongly underestimate organic matter deposition on the seafloor, both in localised settings37,38 as on an ocean-wide scale39. While Global Biogeochemical Ocean Circulation Models (GBOCMs) realistically simulate large-scale oceanic circulation40, they often tend to underestimate the flux of organic matter to the deep seafloor41. Based on our results, part of this discrepancy could result from a too crude parameterisation of the small-scale topographic features within the coarse model grids of GBOCMs and thereby they miss the contribution to the organic matter flux due to topographically-enhanced sequestration.

Our study enhances the mechanistic understanding of the transport of organic matter to CWCs. This knowledge is not only crucially important to understand the functioning of CWCs in the present-day, but also in view of our future oceans, in which the export of organic matter to the deep sea is expected to decrease6 due to increased stratification, with major anticipated consequences for soft-sediment communities42. It is acknowledged that CWCs experience a multitude of stressors that makes them particularly vulnerable to expected global changes. Increased water-column stratification may not only reduce primary production due to nutrient limitation, but may directly reduce the frequency and magnitude of vertical mixing events decreasing the organic matter supply. Simultaneously, organic matter demands will likely increase, both because CWC strongly increase respiration at elevated temperatures43 and because of increased energy demands to sustain calcification rates44 in aragonite-undersaturated seawater caused by ocean acidification in the next decades7. It is clear that only an integrated approach, involving hydrodynamic, biogeochemical and physiological disciplines, will allow forecasting the functioning of precious CWCs in our future oceans.


Material and methods

The Logachev Mound province is situated on the south-western flank of Rockall Bank (NE Atlantic). Mound clusters are several kilometres long and have an elongated shape that follow the isobaths of Rockall Bank and have their summit between 600 and 1000 m water depth15. The summits and rims of these mounds are capped with cold-water corals and their rich associated communities2,16,45. Our conclusions are derived from a coupling of a hydrodynamic, biogeochemical and habitat suitability model, which are described below.

Hydrodynamic model

A hydrodynamic model of the Logachev mounds has been developed by ref. 17 in the Regional Ocean Modeling System (ROMS), which solves the free-surface hydrostatic primitive equations of the fluid dynamics over complex topography using the Boussinesq assumption46,47. The finite difference approximations have stretched, terrain-following coordinates in the vertical and curvilinear Arakawa C-grid coordinates in the horizontal. A nested grid was used with a parent domain of 192 * 188 km, and a child domain of 103 * 61 km. The horizontal spatial resolution of the internal grid (55°21′ to 55°53′ North, 16°16′ to 14°50′ W) was high, comprising 410 * 242 grid cells, each about 250 m wide. Along the vertical, there were 32 sigma levels that provided increased resolution near the bottom and surface boundaries47. The stretching parameters to generate this grid were θs = 3.4, θb = 117. The Northern, Eastern, Southern and Western boundary conditions were imposed as an implicit radiative boundary scheme for water-surface elevation and the 3D momentum, allowing waves to propagate out of the domain. The currents were forced by the global inverse tidal solution TPXO6 48; the model was run for an entire year, but only the results for the situation in April was used. It is important to note that although non-linear internal wave generation is not explicitly resolved by the model, the evolution of internal lee waves and associated large-amplitude up- and downwelling events are well represented17.

Habitat suitability model

The presence of cold-water corals in the area was inferred from a habitat suitability model, which predicts coral occurrence at the Logachev province from a generalised linear modelling approach based on a set of bathymetric, hydrodynamic and environmental variables14. The hydrodynamical variables were extracted from the ROMS model by17 as used in the present study. The model was trained on a coral presence/absence dataset that was collected during dedicated Remotely Operated Vehicle (ROV) transects (±2 m above the seabed, speed 0.3 m/s), providing frames with 117 presences and 227 absences within the Logachev province14. The model performed well after training and predicts coral presence primarily on the summit and flanks of the mounds provinces in the south-western Rockall Bank and on a ridge in the north-western Rockall Bank14.

Organic matter reaction model

The output of the hydrodynamic ROMS model, stored at 6 hour intervals, was used offline to drive organic matter dynamics in the water column, including production at the upper boundary, advective horizontal and vertical transport, constant decay and passive sinking. The ROMS model includes the effects of waves on the ocean currents by a moving surface boundary49. This temporal stretching of the grid was ignored in the simulation of the organic matter dynamics to shorten simulation time. Conservation of momentum was imposed at each time step by calculating the upward flow rate w from the flux divergence of the horizontal flows and assuming that the free-surface elevation (η) is constant and that the vertical velocity at the bottom is zero wz=0 = 0

in which Hz is the grid-cell thickness.

The organic matter in the model is expressed in Carbon equivalent (C). Following the conservation of momentum, the organic matter reaction model is given by:

in which ws is the sinking velocity, and k is the first-order decay rate, both taken as a constant.

Zero-gradient conditions were imposed at the lower and horizontal domain boundaries. At the upper boundary a constant flux of 12 mmol C m−2 d−1 was imposed. This is equivalent to an export carbon flux of about 50 g C m−2 yr−1, consistent with estimates of new production in the nearby Goban Spur area50. The sinking velocity (ws) and the decay rate (k) were chosen such that the e-folding depth (w/k) was around 500–700 m, a value often used in biogeochemical ocean general circulation models39. The sinking velocity of 20 m d−1 and the first-order decay rate of 0.03 d−1 are representative for the decay of freshly produced organic matter51. Note that with this input flux and sinking speed, the maximal organic matter concentration in the water column is 0.6 mmol C m−3. This is below measured organic matter concentrations at northwestern Atlantic margins, ranging from 0.75 mmol C m−3 at Darwin Mounds to 3.7 mmol C m−3 at Logachev mounds and up to 10.8 mmol C m−3 at Porcupine Bank52. However, our model results are representative for reactive, freshly-produced organic matter, while the in situ measurements include refractory organic matter.

Deposition of organic matter from the water column to the seafloor is due to passive sinking. In the CWC areas however, the deposition of organic matter is due to both passive sinking and suspension-feeding. Feeding by passive (e.g. corals, anemones and soft-corals) and active (e.g. bivalves and sponges) suspension feeders is often expressed in units of m3 m−2 d−1 = m d−1, which, when multiplied with the OM concentration in the water column, gives total OM uptake rates53. This expression is mathematically similar to the expression for passive sinking, so that suspension feeding can be accounted for by increasing the passive settling velocity (ws). The passive sinking velocity in the bottom grid cells overlying the CWCs was enhanced by a factor 10 to account for the suspension feeding activity, giving a ws of 200 m d−1. Note that the organic matter deposition presented in Fig. 5A can be easily back-calculated into ‘passive settling’ and ‘suspension feeding’ using this enhancement factor. The enhancement factor of 10 can be justified by the following three arguments. Firstly, the metabolic activity of a cold-water coral community is 5 to 10 times higher as compared to the adjacent barren seafloor2,3,23,24. The enhancement factor 10 is needed to ensure that sufficient organic matter was taken up by the reef community to sustain their elevated metabolic activity. Secondly, while in situ estimates of ws above CWC reefs are not available, our enhancement factor compares favourably with data from tropical coral reefs53. These authors estimated grazing rates (conceptually comparable to ws) for tropical reefs of −60 (when reefs are a net source of organic matter) up to 180 m d−1. As CWC reefs cannot be net sources of organic matter and the friction velocities are typically higher than on tropical reefs54, the higher values for ws from53 are more reasonable for CWC reefs. Thirdly, an order of magnitude calculation of the capturing efficiency shows that the assumed ws is not unrealistic. The mean current velocity is roughly 0.3 m s−1 above the CWCs. Assuming that suspension feeders feed from 20 cm of water above the sediment (a lower estimate, as corals are usually higher than 20 cm), this means that a m2 of CWC reef can extract resources from 5184 m3 d−1. With the imposed suspension feeding rate of 200 m d−1, this implies that they have a capturing efficiency of less than 4%.

The biogeochemical transport-reaction equations were numerically solved on a staggered grid (Arakawa C-grid) with the organic matter concentration defined in the centre of each box and the flows on the grid cell interfaces. The six-hourly velocity data from the hydrodynamic model were linearly interpolated in time to obtain velocity fields at each model integration step. The organic matter model comprised about 2.5 · 106 equations and was numerically integrated using a variable-order Adams-Moulton predictor-corrector scheme, as implemented in the R-package deSolve55 running in the open-source software R56. Advection was implemented using simple first-order upwind differencing; due to the numerical dispersion that this generates, no horizontal or vertical dispersion was used. The vertical diffusivities as generated by the hydrodynamic model were in fact very low.

Additional Information

How to cite this article: Soetaert, K. et al. Ecosystem engineering creates a direct nutritional link between 600-m deep cold-water coral mounds and surface productivity. Sci. Rep. 6, 35057; doi: 10.1038/srep35057 (2016).


  1. Henry, L.-A. & Roberts, J. M. Biodiversity and ecological composition of macrobenthos on cold-water coral mounds and adjacent off-mound habitat in the bathyal Porcupine seabight, (NE) Atlantic. Deep-Sea Res. I 54, 654–672 (2007).

    Google Scholar 

  2. van Oevelen, D. et al. The cold-water coral community as a hot spot for carbon cycling on continental margins: A food-web analysis from Rockall Bank (Northeast Atlantic). Limnol. Oceanogr. 54, 1829–1844 (2009).

    ADS  Google Scholar 

  3. Cathalot, C. et al. Cold-water coral reefs and adjacent sponge grounds: Hotspots of benthic respiration and organic carbon cycling in the deep sea. Front. Mar. Sci. 2, 37. doi: 10.3389/fmars.2015.00037 (2015).

    Article  Google Scholar 

  4. Suess, E. Particulate organic carbon flux in the oceans - surface productivity and oxygen utilization. Nature 288, 260–263 (1980).

    ADS  CAS  Google Scholar 

  5. Wohlers, J. et al. Changes in biogenic carbon flow in response to sea surface warming. Proc. Natl Acad. Sci. USA 106, 7067–7072 (2009).

    ADS  CAS  PubMed  Google Scholar 

  6. Bopp, L. et al. Potential impact of climate change on marine export production. Global Biogeochem. Cy. 15, 81–99 (2001).

    ADS  CAS  Google Scholar 

  7. Guinotte, J. M. et al. Will human-induced changes in seawater chemistry alter the distribution of deep-sea scleractinian corals? Front. Ecol. Environ. 4, 141–146 (2006).

    Google Scholar 

  8. Form, A. U. & Riebesell, U. Acclimation to ocean acidification during long-term CO2 exposure in the cold-water coral Lophelia pertusa. Glob. Change Biol. 18, 843–853 (2012).

    ADS  Google Scholar 

  9. Roberts, J. M., Wheeler, A. J. & Freiwald, A. Reefs of the deep: The biology and geology of cold-water coral ecosystems. Science 312, 543–547 (2006).

    ADS  CAS  PubMed  Google Scholar 

  10. Davies, A. et al. Downwelling and deep-water bottom currents as food supply mechanisms to the cold-water coral Lophelia pertusa (scleractinia) at the Mingulay Reef complex. Limnol. Oceanogr. 54, 620–629 (2009).

    ADS  Google Scholar 

  11. Wagner, H., Purser, A., Thomsen, L., Jesus, C. & Lundalv, T. Particulate organic matter fluxes and hydrodynamics at the Tisler cold-water coral reef. J. Mar. Syst. 85, 19–29 (2011).

    Google Scholar 

  12. Findlay, H. S. et al. Tidal downwelling and implications for the carbon biogeochemistry of cold-water corals in relation to future ocean acidification and warming. Glob. Change Biol. 19, 2708–2719 (2013).

    ADS  Google Scholar 

  13. White, M., Murray Roberts, J. & van Weering, T. Do bottom-intensified diurnal currents shape the alignment of carbonate mounds in the NE Atlantic? Geo-Mar. Lett. 27, 391–397 (2007).

    ADS  CAS  Google Scholar 

  14. Rengstorf, A. M., Mohn, C., Brown, C., Wisz, M. S. & Grehan, A. J. Predicting the distribution of deep-sea vulnerable marine ecosystems using high-resolution data: Considerations and novel approaches. Deep-Sea Res. I 93, 72–82 (2014).

    Google Scholar 

  15. van Weering, T., de Haas, H., De Stigter, H., Lykke-Andersen, H. & Kouvaev, I. Structure and development of giant carbonate mounds at the SW and SE Rockall Trough Margins, NE Atlantic Ocean. Mar. Geol. 3313, 1–15 (2003).

    Google Scholar 

  16. Mienis, F. et al. Hydrodynamic controls on cold-water coral growth and carbonate-mound development at the SW and SE Rockall Trough Margin, NE Atlantic Ocean. Deep-Sea Res. I 54, 1655–1674 (2007).

    Google Scholar 

  17. Mohn, C. et al. Linking benthic hydrodynamics and cold-water coral occurrences: A high-resolution model study at three cold-water coral provinces in the NE Atlantic. Progr. Oceanogr. 122, 92–104 (2014).

    ADS  Google Scholar 

  18. Dewey, R., Richmond, D. & Garrett, C. Stratified tidal flow over a bump. J. Phys. Oceanogr. 35, 1911–1927 (2005).

    ADS  MathSciNet  Google Scholar 

  19. Jackson, C. R., da Silva, J. C. B. & Jeans, G. The generation of nonlinear internal waves. Oceanography 25, 108–123 (2012).

    Google Scholar 

  20. Legg, S. & Klymak, J. Internal hydraulic jumps and overturning generated by tidal flow over a tall steep ridge. J. Phys. Oceanogr. 38, 1949–1964 (2008).

    ADS  Google Scholar 

  21. Cyr, F., Van Haren, H., Mienis, F., Duineveld, G. & Bourgault, D. On the influence of cold-water coral mound size on flow hydrodynamics, and vice versa. Geophys. Res. Lett. 43 (2016).

  22. Mueller, C. E. et al. Opportunistic feeding on various organic food sources by the cold-water coral Lophelia pertusa. Biogeosciences 11, 123–133 (2014).

    ADS  Google Scholar 

  23. White, M. et al. Cold-water coral ecosystem (Tisler Reef, Norwegian Shelf) may be a hotspot for carbon cycling. Mar. Ecol. Progr. Ser. 465, 11–23 (2012).

    ADS  CAS  Google Scholar 

  24. Rovelli, L. et al. Benthic O2 uptake of two cold-water coral communities estimated with the non-invasive eddy-correlation technique. Mar. Ecol. Progr. Ser. 525, 97–104 (2015).

    ADS  Google Scholar 

  25. White, M. & Dorschel, B. The importance of the permanent thermocline to the cold water coral carbonate mound distribution in the NE Atlantic. Earth Planet. Sc. Lett. 296, 395–402 (2010).

    ADS  CAS  Google Scholar 

  26. Van Haren, H., Mienis, F., Duineveld, G. C. A. & Lavaleye, M. S. S. High-resolution temperature observations of a trapped nonlinear diurnal tide influencing cold-water corals on the Logachev Mounds. Prog. Oceanogr. 125, 16–25 (2014).

    ADS  Google Scholar 

  27. Roberts, J. M., Wheeler, A., Freiwald, A. & Cairns, S. Cold-water corals. The biology and geology of deep-sea coral habitats (Cambridge University Press, Cambridge, 2009).

  28. White, M., Mohn, C., de Stigter, H. & Mottram, G. Deep-water coral development as a function of hydrodynamics and surface productivity around the submarine banks of the Rockall Trough, NE Atlantic. 503–514 (Springer, Heidelberg, 2005).

  29. Mohn, C. & White, M. Seamounts in a restless ocean: Response of passive tracers to sub-tidal flow variability. Geophys. Res. Lett. 37 (2010).

  30. Frederiksen, R., Jensen, A. & Westerberg, H. The distribution of the scleractinian coral Lophelia pertusa around the Faroe Islands and the relation to internal tidal mixing. Sarsia 77, 157–171 (1992).

    Google Scholar 

  31. Thiem, O., Ravagnan, E., Fosså, J.-H. & Berntsen, J. Food supply mechanisms for cold-water corals along a continental shelf edge. J. Mar. Syst. 60, 207–219 (2006).

    Google Scholar 

  32. Huvenne, V. A. I. et al. A picture on the wall: innovative mapping reveals cold-water coral refuge in submarine canyon. PLoS One 6, e28755 (2011).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  33. Dullo, W.-C., Flögel, S. & Rüggeberg, A. Cold-water coral growth in relation to the hydrography of the Celtic and Nordic European continental margin. Mar. Ecol. Progr. Ser. 371, 165–176 (2008).

    ADS  Google Scholar 

  34. Davies, A. J. & Guinotte, J. M. Global habitat suitability for framework-forming cold-water corals. Plos One 6, e18483 (2011).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  35. Jones, C. G., Lawton, J. H. & Shachak, M. Organisms as ecosystem engineers. Oikos 69, 373–386 (1994).

    Google Scholar 

  36. Yesson, C., Clark, M., Taylor, M. & Rogers, A. The global distribution of seamounts based on 30 arc seconds bathymetry data. Deep-Sea Res. I 58, 442–453 (2011).

    Google Scholar 

  37. Smith, K. Jr Food energy supply and demand: A discrepancy between particulate organic carbon flux and sediment community oxygen consumption in the deep ocean. Limnol. Oceanogr. 32, 201–220 (1987).

    ADS  Google Scholar 

  38. Herman, P. M. et al. The seafloor as the ultimate sediment trap using sediment properties to constrain benthic-pelagic exchange processes at the Goban Spur. Deep-Sea Res. II 48, 3245–3264 (2001).

    ADS  Google Scholar 

  39. Andersson, J. et al. Respiration patterns in the deep sea. Geophys. Res. Lett. 31 (2004).

  40. Doney, S. C. et al. Evaluating global ocean carbon models: The importance of realistic physics. Global Biogeoch. Cy. 18 (2004).

  41. Kriest, I. & Oschlies, A. Swept under the carpet: organic matter burial decreases global ocean biogeochemical model sensitivity to remineralization length scale. Biogeosciences 10, 8401–8422 (2013).

    ADS  Google Scholar 

  42. Jones, D. et al. Global reductions in seafloor biomass in response to climate change. Glob. Change Biol. 20, 1861–1872 (2014).

    ADS  Google Scholar 

  43. Dodds, L. A., Roberts, J. M., Taylor, A. C. & Marubini, F. Metabolic tolerance of the cold-water coral Lophelia pertusa (scleractinia) to temperature and dissolved oxygen change. J. Exp. Mar. Biol. Ecol. 349, 205–214 (2007).

    CAS  Google Scholar 

  44. McCulloch, M. et al. Resilience of cold-water scleractinian corals to ocean acidification: Boron isotopic systematics of pH and saturation state up-regulation. Geochim. Cosmochim. Acta 87, 21–34 (2012).

    ADS  CAS  Google Scholar 

  45. Biber, M. F. et al. Investigating the association of fish abundance and biomass with cold-water corals in the deep Northeast Atlantic Ocean using a generalised linear modelling approach. Deep-Sea Res. II 99, 134–145 (2014).

    Google Scholar 

  46. Shchepetkin, A. F. & McWilliams, J. C. The regional oceanic modeling system (roms): a split-explicit, free-surface, topography-following-coordinate oceanic model. Ocean Model. 9, 347–404 (2005).

    ADS  Google Scholar 

  47. Haidvogel, D., Blanton, J., Kindle, J. & Lynch, D. Coastal ocean modelling: processes and real-time systems. Oceanography 13, 35–46 (2000).

    Google Scholar 

  48. Egbert, G. & Erofeeva, S. Efficient inverse modeling of barotropic ocean tides. J. Atmos. Oceanic Tech. 19 (2002).

  49. Warner, J., Sherwood, C., Signell, R., Harris, C. & Arango, H. Development of a three-dimensional, regional, coupled wave, current, and sediment-transport model. Comput. Geosci. 34, 1284–1306 (2008).

    ADS  Google Scholar 

  50. Joint, I. et al. Pelagic production at the Celtic Sea shelf break. Deep-Sea Res. II 48, 3049–3081 (2001).

    ADS  Google Scholar 

  51. Westrich, J. T. & Berner, R. A. The role of sedimentary organic matter in bacterial sulphate reduction: The g model tested. Limnol. Oceanogr. 29, 236–249 (1984).

    ADS  CAS  Google Scholar 

  52. Kiriakoulakis, K., Freiwald, A., Fisher, E. & Wolff, G. Organic matter quality and supply to deep-water coral/mound systems of the NW European continental margin. Int. J. Earth Sci. 96, 159–170 (2007).

    CAS  Google Scholar 

  53. Monismith, S. G. et al. Flow effects on benthic grazing on phytoplankton by a Caribbean reef. Limnology and Oceanography 55, 1881–1892 (2010).

    ADS  Google Scholar 

  54. Guihen, D., White, M. & Lundälv, T. Boundary layer flow dynamics at a cold-water coral reef. Journal of Sea Research 78, 36–44 (2013).

    ADS  Google Scholar 

  55. Soetaert, K., Petzoldt, T. & Setzer, R. Solving differential equations in R: Package deSolve. J. Stat. Softw. 33, 1–25 (2010).

    Google Scholar 

  56. R. Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria URL (2014).

  57. Freiwald, A., Rogers, A. & Hall-Spencer, J. Global distribution of cold-water corals (version 2). Update of the dataset in Freiwald et al. (2004). Cambridge (UK): UNEP World Conservation Monitoring Centre, URL (2005).

  58. Hebbeln, D. et al. Environmental forcing of the Campeche cold-water coral province, Southern Gulf of Mexico. Biogeosciences 11, 1799–1815 (2014).

    ADS  Google Scholar 

  59. Correa, T. B., Eberli, G. P., Grasmueck, M., Reed, J. K. & Correa, A. M. Genesis and morphology of cold-water coral ridges in a unidirectional current regime. Mar. Geol. 326–328, 14–27 (2012).

    ADS  Google Scholar 

  60. Eisele, M. et al. Productivity controlled cold-water coral growth periods during the last glacial off Mauritania. Mar. Geol. 280, 143–149 (2011).

    ADS  CAS  Google Scholar 

  61. Savini, A. & Corselli, C. High-resolution bathymetry and acoustic geophysical data from Santa Maria di Leuca cold-water coral province (Northern Ionian Sea–Apulian continental slope). Deep-Sea Res. II 57, 326–344 (2010).

    ADS  Google Scholar 

Download references


This work was supported by the CoralFISH project (EU-FP7 grant agreement number 213144), the Netherlands Organisation for Scientific Research (VIDI grant no. 864.13.007 to DvO) and has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 678760 (ATLAS). This output reflects only the author’s view and the European Union cannot be held responsible for any use that may be made of the information contained therein.

Author information




The authors declare no conflict of interest. K.S. and D.v.O. wrote the manuscript, K.S., A.G. and C.M. designed the modeling approach, K.S., C.M., A.R. and D.v.O. performed and analysed the model results, and all authors discussed the results.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Electronic supplementary material

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Soetaert, K., Mohn, C., Rengstorf, A. et al. Ecosystem engineering creates a direct nutritional link between 600-m deep cold-water coral mounds and surface productivity. Sci Rep 6, 35057 (2016).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing