The ability of coral reefs to engineer complex three-dimensional habitats is central to their success and the rich biodiversity they support. In tropical reefs, encrusting coralline algae bind together substrates and dead coral framework to make continuous reef structures, but beyond the photic zone, the cold-water coral Lophelia pertusa also forms large biogenic reefs, facilitated by skeletal fusion. Skeletal fusion in tropical corals can occur in closely related or juvenile individuals as a result of non-aggressive skeletal overgrowth or allogeneic tissue fusion, but contact reactions in many species result in mortality if there is no ‘self-recognition’ on a broad species level. This study reveals areas of ‘flawless’ skeletal fusion in Lophelia pertusa, potentially facilitated by allogeneic tissue fusion, are identified as having small aragonitic crystals or low levels of crystal organisation and strong molecular bonding. Regardless of the mechanism, the recognition of ‘self’ between adjacent L. pertusa colonies leads to no observable mortality, facilitates ecosystem engineering and reduces aggression-related energetic expenditure in an environment where energy conservation is crucial. The potential for self-recognition at a species level and subsequent skeletal fusion in framework-forming cold-water corals is an important first step in understanding their significance as ecological engineers in deep-seas worldwide.
Tropical scleractinian coral reefs are largely consolidated by photosynthetic coralline algae that bind coral framework and sediment to create extensive shallow-water reef systems. However, coral reefs are not restricted to tropical waters and reef framework forming cold-water corals are found in deep-water continental shelf, slope and seamount settings across the globe (Fig. 1). Of these corals, Lophelia pertusa is the most globally widespread and forms extensive carbonate framework reefs1. Since Lophelia-engineered reef systems are mostly below the photic zone, coralline algae are not available to bind the reefs together. In such cold-water coral reefs, consolidation is facilitated by skeletal fusion between individual L. pertusa colonies that are over several years of age (assuming annual polyp division)2.
While it is known that L. pertusa branches within individual colonies routinely fuse, it is often impossible to identify where fusion has occurred between different colonies. In cases where fusion has been identified, it has been assumed that both colonies were closely related and were displaying characteristics which have also been noted in tropical corals3,4,5.
True skeletal fusion in tropical corals occurs in conjunction with allogeneic tissue fusion, which is controlled by allorecognition, a major characteristic in invertebrate immunity4 that depends upon the ability to recognise self and non-self4,6. In tropical corals, the ability to allorecognise depends largely on the maturity of the individuals with allogeneic fusion only reported in juvenile corals. In tropical corals it is thought that the lack of an active historecognition system during the early stages of ontogeny (4–8 months) allows juveniles of the same species to occasionally allogeneically fuse6,7,8. However, allorecognition in corals is a complex synergy of effector mechanisms, specificity and competency4,6,9, which may have evolved as far back as 400 million years ago10. Allogeneic interactions between juvenile tropical corals fall into three groups: (A) true fusion (resulting in a chimaera), (B) incompatible fusion, or (C) non-fusion6. True fusion will often be followed by incompatible fusion, when one colony reaches historecognition maturity or starts to discriminate between self and non-self. At this point, skeletal ridges or overgrowth may occur but, importantly, continuous framework will have been established between colonies8.
This study examines the ability of L. pertusa to achieve skeletal fusion between genetically distinct individuals. If genetically distinct L. pertusa colonies reacted aggressively when they came into contact, as is the case for some adult genetically distinct tropical corals3,11, the reef frameworks built by this species would not be as large or as stable given the absence of encrusting coralline algae. The skeletal fusion reported for the first time in this study is either the result of allogeneic fusion followed by incompatible fusion, or efficient, low aggression overgrowth of one individual into another as a result of self-recognition on a species level3. The low aggression between individuals is apparent by the visible lack of a ‘dead-zone’ where no tissue covers the skeleton, or a very small area (<1 mm), as opposed to the larger dead zones that are noted following tropical coral contact reactions3,11. This could indicate either a lack of aggression or a reduced form of aggression compared to tropical corals. Regardless of whether allogeneic fusion or low-aggression efficient overgrowth is most prevalent, or whether both occur, the degree of observed skeletal fusion on L. pertusa reefs12 highlights how self-recognition on a species level underpins the success of this key ecosystem engineer.
Several skeletal fusion instances were observed in adult L. pertusa colonies (Fig. 2A). Ridges and skeletal overgrowth is apparent in Fig. 2A and B, where an orange polyp has been encased by white skeleton. Where multiple contact events between two polyps are observed (Fig. 2C), possible reversal of overgrowth is observed, as orange tissue re-grew over white skeleton. The dominant coral in this case through non-transitive hierarchy is not clear, which is consistent with observations that white and orange colonies of L. pertusa remain distinct (i.e. separate individuals) beyond their sites of initial and continued fusion (Fig. 2D). If one colony was ‘dominant’, it could be expected that a large proportion of overgrowth by that colony would occur as a result of dominant aggression.
Cross-sectional SEM imaging of a fusion contact zone reveals instances where there is no clear demarcation of one polyp ending and another beginning, indicating full skeletal fusion (Fig. 3A–D). However, a ‘micro-suture’ between the orange and white polyp (Fig. 3E, F) ranging from <1 to 3 μm is visible in parts of the sample. The orange polyp has a highly organised crystallographic structure near the micro-suture (Fig. 3F, using Electron Back Scatter Diffraction (EBSD)). In contrast, the white polyp appears to either have crystals too small for visualisation, or a high organic content (e.g. Cusack et al.13). While individual crystal orientation may change depending upon the cross-section location, the lack of crystallographic organisation in the white polyp compared to the orange polyp (Fig. 3E, F) differs to crystallographic organisation in non-fused white L. pertusa polyp examples (see Fig. S1), where large, well-organised aragonite crystals are identifiable in a variety of orientations. Cavities were also identified near fusion zones and in both polyps, where crystals appear to originate from different centres of calcification. Micro-sutures also originate from these holes, with diffraction and crystallographic orientation indicating that aragonite crystals interlocked successfully (Fig. 4A–C).
Changes in the physical structure of the skeleton at the different fusion zones were identified by using Raman spectroscopy. A decrease in the width (Full Width Half Maximum, FWHM) of the ca. 1085 cm−1 peak indicates decreased calcium carbonate bond lengths15. These shorter bond lengths are stronger, but are the result of greater molecular disorder14,15. Where no micro-suture was identified between the white and orange polyps (Fig. 3C), the FWHM was significantly smaller than the FWHM of the white polyp where a large (ca. 2 μm) micro-suture was evident (Mann-Whitney U = 0.00, p = 0.036, d.f. = 6) (Fig. 5B), but not significantly smaller than the orange polyp. FWHMs (n = 3) of both polyps at the small micro-suture (<1 μm) were smaller than at a large suture, but this difference was not significant. FWHM on both polyps on the opposite side to fusion events were markedly different from each other (Fig. 5C). To account for variability in FWHM being potentially caused by crystal size, orientation and potential organic content, transects were taken at fusion areas (Fig. 5A, S1). The differences described above, where FWHM was lower at the sutureless zone compared to suture zones were still observed as distance away from the suture increased and hence represented biologically controlled differences and not artefacts of the cross-section location.
Maximum-likelihood estimates of relatedness (r) were generated from multi-locus genotypes, including 15 microsatellite markers, for L. pertusa individuals from Nordleksa and Sula Ridge sites. Relatedness estimates ranged from 0.00 (unrelated, 148 of 182 pairwise comparisons) to 0.66 (full siblings, 4 Sula Ridge comparisons), with 3 Sula Ridge comparisons estimated to be half-sibs (r = 0.32) (Table 1). The two fused individuals were classified as unrelated in the analysis (r = 0.00) and the probability that these individuals were unrelated did not change when the frequencies of null alleles were included.
The ability of L. pertusa to skeletally fuse12 between individuals has facilitated their roles as deep-sea ecosystem engineers. Here we demonstrate that this can occur between genetically distinct adult individuals and not just between closely related individuals. It is likely that this ability has been driven by two main factors: 1) evolutionary pressure for cold-water corals to stabilise their own framework, much like the role of calcifying encrusting algae on tropical reefs and 2) the benefit of reducing energetic investment into aggressive competition interactions, which can lead to mortality or reductions in growth and gonad development in reef forming corals11. Creation of continuous reef frameworks would ensure suitable substrate is formed for the settlement of subsequent generations providing a selective advantage. Skeletal fusion would also act to prevent unnecessary coral death if the underlying framework is broken e.g. from strong currents and/or bioerosion, as live coral branches falling into other colonies would be more likely to survive and grow. Since deep-water corals rely purely on heterotrophic feeding (i.e. feeding on passing prey items, which varies spatially and temporally) avoiding unnecessary energetic expenditure, which could be reallocated to growth and reproduction, would be of significant benefit to the success and continuation of L. pertusa reefs.
Further work is needed to identify whether this skeletal fusion is driven by: 1) allogeneic fusion between individuals, or 2) an efficient, minimally aggressive ‘overgrowth’ strategy across individuals that does not result in mortality of any polyps. Both of these mechanisms are represented here and both rely on a high degree of self-recognition at a species level. Efficient overgrowth with no observable mortality is apparent in Fig. 2B and C and potential allogeneic tissue fusion is identifiable in Fig. 3A, leading to seamless skeletal fusion (Fig. 3.D). The skeletal fusion reported here between genetically distinct individuals with unique multi-locus genotypes at 15 microsatellite loci, underpins the fact that while L. pertusa can discriminate ‘self’ on a species level, they do not reject between individuals. The occurrence of both overgrowth and potential allogeneic fusion in data presented here complements observations that allogeneic fusion is complex and can happen in a series of cascading events6. For the rare instances that adult allogeneic fusion has been noted in tropical corals16, they are typically explained by a close genetic similarity of the colonies involved4,5.
The difference between overgrowth and tissue allogeneic fusion may be represented in: 1) the strength or molecular organisation of the aragonite bonds14,15 and 2) the organisation or size of aragonite crystals. For 1) the decreased FWHM at the suture-less fusion zone indicates decreased molecular organisation but stronger bonding within the aragonite. FWHM in areas with small micro-sutures and larger micro-sutures increased respectively. It seems that full skeletal fusion where no suture is formed, results in strong molecular bonding and potentially small, or disorganised crystal bundles compared to areas where sutures were apparent. Allogeneically fused tissue could thus result in different biomineralisation properties of the coral skeleton. In areas that may be the result of overgrowth, decreased aragonite bond strength of one or both of the polyps, or increased crystallographic organisation is observed. It is unknown how these factors are controlled when contact does occur between corals and whether the cavities that are observed near the fusion zones are a result of fusion-skeletal effectors, or the result of overgrowth of organic debris while the coral was growing.
Aside from the specific mechanisms that facilitate this skeletal fusion, it is also unknown whether this ability is limited to the deep-water coral L. pertusa or whether other deep-water reef framework-forming species (see Fig. 1) also exhibit skeletal and potential allogeneic fusion, between non-kin adult individuals. Regardless of whether the large, multi-colony frameworks which are often characteristic of L. pertusa reefs are mostly a result of allogeneic tissue fusion or efficient low aggression overgrowth, the ability of L. pertusa to self-recognise at a species level to routinely undergo skeletal fusion has made them one of the most significant ecosystem engineers of the deep seas.
The fused orange and white L. pertusa colony and additional orange and white L. pertusa genetic material from Nordleksa reef and Sula ridge (Fig. 1) were first observed from and then collected using the two-man submersible JAGO (GEOMAR, Kiel, Germany) in September 2011. To record observations through HD video and still images, LED Multi-Sealite Matrix (DeepSea Power and Light) lights, a Sony HVR-V1E (HDV1080i) video camera and a custom-housed GoPro HD Hero 3 camera were used. Genetic subsamples from the fused corals and neighbouring colonies were collected and stored using FTA cards (Whatman).
Total DNA was isolated from L. pertusa tissue preserved on the cards using the tissue protocol from the PureGene DNA extraction kit (Gentra Systems, Inc., Minneapolis, Minnesota). PCR conditions for the amplification of L. pertusa microsatellite loci followed Morrison et al.17. Fluorescent DNA fragments were multiplexed and analysed on an ABI 3130XL Genetic Analyzer (Applied Biosystems) with Genescan-500 LIZ size standard. Genemapper fragment analysis software (Applied Biosystems) was used to score, bin and output allelic data. The program GenAlEx 6.518,19 provided summary statistics for the dataset including heterozygosity and alleles per locus. Genetic relatedness between individuals was estimated as the probability that individuals share zero, one or two alleles per marker that are identical by descent20 with a maximum-likelihood based estimator in the program ML-RELATE21. Since the presence of null alleles can impact the accuracy of relatedness estimates22, the presence of null alleles was tested for each locus and their frequencies estimated in ML-RELATE prior to relatedness analyses.
Characteristics of the fifteen polymorphic loci17 to analyse relatedness are detailed in Table S1. Markers yielded between 4 and 13 alleles with an average of 9.3 alleles and a mean expected heterozygosity of 0.758 (Table S1). Deviations from Hardy-Weinberg Equilibrium were observed, with 8 out of the 15 loci showing heterozygote deficits.
To assess the biomineralisation aspects of a fused zone, the fused section pictured in Fig. 3 was set in EpoHeat epoxy (Buehler) and cross-sectioned using a slow-speed saw. The sample was polished using progressive grits (320, 1200, 2500, 4000), micropolished using alpha aluminium oxide at 1 and 0.3 μm and then fine-polished with 0.06 μm amorphous colloidal silica (Buehler) on a short nap to remove any residual damaged surface layers13. Back scatter electron micrographs of the entire cross section and likely points of fusion were then taken using an FEI Quanta 200F field emission scanning electron microscope (SEM) equipped with a TSL EBSD system and OIM version 6 at the University of Glasgow.
Grain CI tolerance was 5 with a minimum grain size of 2 pixels, neighbour CI correlation was CI 0.05. The Kikuchi patterns were indexed using the OIM Data Collection database, which contains structure files of aragonite. OIM maps were subject to two clean-up algorithm procedures to ensure reliable data were displayed, where grain CI standardization was applied with a grain tolerance angle of 5, minimum grain size of 2 pixels and neighbour CI correlation of CI 0.2. Further partitioning of data was applied with only grains of CI Fit and displayed in the resultant OIM map to remove any background noise from the final dataset as in Cusack et al.13.
To assess the molecular properties of the skeleton, Raman spectroscopy was used as described by Kamenos et al.14. The aragonite peak in L. pertusa is centred at ca. 1085 cm−1. Raman data were collected along transects (3 replicates) along zones of interest in the sample. This included: 1) the area directly below where the samples are fused at their uppermost point, 2) zones where the micro-suture is relatively large (>1 μm) and small (<1 μm) and 3), zones on both polyps which were not involved in fusion. The full width at half maximum (FWHM) of the ca. 1085 cm−1 is related to positional disorder of the lattice and in turn molecular bond strength15. Increases in molecular bond strength can be attributed to positional disorder of crystal lattice via ions moving out of the plane parallel to the a-axis in the direction of the c-axis15.
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We thank the JAGO submersible team for their skill at sea, U. Riebesell and the BIOACID project for the opportunity to join RV Poseidon cruise P420 along with Captain Windscheid and the crew for excellent support and the Norwegian Directorate of fisheries (Fiskeridirektoratet). We would also like to thank E. Dyrynda, G. Cook, L. Henry and M. Wisshak for insightful comments on this manuscript and Peter Chung for microscopy help. Images 2A–C and 3A were taken by Solvin Zankl, Image 2D was taken by the JAGO submersible team, GEOMAR, Kiel. Molecular lab work was done by M. Springmann and the coral distribution map was compiled by M. Mellado-Silva. This paper is a contribution to the UK Ocean Acidification Research Programme to J.M.R. and N.K. (NERC grant NE/H017305/1), a NERC Independent Research Fellowship to S.J.H. (NE/K009028/1), BIOACID (BMBF, FKZ 03F0655A), a Royal Society of Edinburgh IRF to N.K. (48704/1) and the European Commission's Seventh Framework Programme (FP7/2007–2013) projects EPOCA (grant agreement no. 211384) and HERMIONE (grant agreement no. 226354) to J.M.R. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. government.
The authors declare no competing financial interests.
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Hennige, S., Morrison, C., Form, A. et al. Self-recognition in corals facilitates deep-sea habitat engineering. Sci Rep 4, 6782 (2014). https://doi.org/10.1038/srep06782
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