Like many other groups of organism macroalgae are known to influence the growth, survival and reproduction of other organisms in their vicinity by producing allelochemicals. Early studies on macroalgal allelopathy predominantly focused on four main categories of effects: (1) regulation of algal populations, (2) regulation of invertebrate colonization, (3) lethal and sublethal effects on fishes and (4) antimicrobial activities1,2. By far, allelopathic defensive functions against herbivores have been the most extensively studied role for macroalgal secondary metabolites over the past 30 years3. More recent studies also revealed the role of allelopathy in the competition with benthic competitors other than algae and notably with corals4. A series of studies demonstrated that some macroalgae possess allelochemicals with bleaching properties on specific coral species5,6,7,8. Allelopathy against corals has been suggested in the brown algal genus Lobophora J. Agardh (Dictyotales, Phaeophyceae). But while Lobophora exhibits a wide array of bioactivities (e.g. antibacterial, antifungal, antiviral) see9 for review, a limited number of studies were directed towards understanding the ecological roles of Lobophora natural products e.g.8,10,11,12,13. Nevertheless, Lobophora remains an important benthic component of tropical coral reefs and species of this genus are commonly observed interacting with scleractinian corals in the Caribbean14,15 and in the Pacific16,17. Among the macroalgae present in the southwestern lagoon of New Caledonia, Lobophora is most commonly encountered in association with scleractinian corals. A review on the species diversity in New Caledonia indicated that the genus is a lot more diverse than reported in the literature18 with at least 31 species, present in New Caledonia. Furthermore, species closely associated with scleractinian corals predominantly belong to a specific clade. Lobophora species have apparently developed very specific ecological niches together with morphologies. For instance, four species of Lobophora with decumbent to encrusting growth forms are in direct contact with corals (i.e. L. hederacea, L. monticola, L. rosacea, L. undulata), while other species with different morphologies were found growing in different habitats and substrates18. Association with corals, except in some rare cases19, did not represent an apparent threat for corals, but rather a shelter for algae from herbivores20. Nevertheless, Lobophora has been considered a potent competitor against corals, particularly following the dramatic regime shift in the Caribbean and Great Barrier Reef16,21,22,23. Subsequently, several studies have aimed at studying Lobophora-coral interactions and understanding the mechanisms by which species of Lobophora may outcompete corals. Dead coral surface is generally a prerequisite for the algal settlement while only a limited number of living coral species seem vulnerable to Lobophora overgrowth24,25,26,27. However, two studies showed that Lobophora allelochemicals presented bleaching properties against three coral species, Porites astreoides, P. cylindrica and Montastraea cavernosa8,11. Conversely, one study demonstrated that Lobophora waterborne compounds enabled coral recruitment12. Overall, Lobophora association with corals has been largely interpreted as negative, even though only a limited number of studies convincingly demonstrated that Lobophora could pose an important threat to corals.

Taking into account that: (1) some Lobophora species are naturally occurring associated with coral species on healthy reefs without apparent signs of competition towards their coral “hosts”, and; (2) that Lobophora organic extracts displayed allelopathy against some coral species in bioassay experiments, we address the following questions: Do Lobophora species naturally found in association with corals present negative allelopathy against the latter; are all Lobophora species, regardless of their association with corals, equally susceptible to bleach corals; and last, if allelopathic interactions are at play, which compounds mediate these interactions? To tackle these questions, we implemented a multi-level approach of allelopathic bioassays starting from a multi-species and crude extract level to a single species and isolated compounds level. We first tested and compared allelopathy effects of several species of Lobophora crude extracts against several species of corals. Then, we compared the negative allelopathy of numerous semi-purified fractions and purified compounds from a single Lobophora species on the most vulnerable coral.


Importance of Lobophora–corals associations in New Caledonia

Association between Lobophora and corals occurs in a variety of habitats, ranging from coral-dominated to algal-dominated communities. We monitored 78 transects in the southwest lagoon and detected Lobophora species associated with corals in 54 transects (69%) (Table 1). Restricting ourselves to transects in which Lobophora was present, the average percentage of associations of this species ranged from 7 to 24%. Three species, L. abscondita, L.crassa and L. nigrescens were never associated with corals. Instead these species grew on a variety of substrates such as dead coral rubble and bedrock (Table 1).

Table 1 Association of Lobophora species with corals in the southwest lagoon of New Caledonia.

Lobophora species are associated with a limited number of coral genera. Association between Lobophora and Acropora is by far the most common. Except in the case of L. hederacea where the alga appears to have deleterious effects on the Seriatopora coral19, living parts of other corals were not overgrown by Lobophora nor presented evident traces of bleaching. Lobophora predominantly grew at the dead basal parts of branching coral colonies. In the case of L. rosacea, the alga forms dense rosettes niched within the coral branches. In the case of L. hederacea and L. monticola the alga attaches itself to the coral base and adopts decumbent forms, while L. dimorpha adopts a procumbent form.

Effects of Lobophora spp. extracts on corals

All extracts prepared from Lobophora species caused significant visual bleaching on the corals A. muricata and S. pistillata and suppression of photosynthetic efficiency in situ, relative to controls (p < 0.001), while no significant bleaching effects were detected in P. cylindrica and M. hirsuta (Fig. 1). In general, A. muricata was more pronouncedly bleached than S. pistillata (Fig. 1). No significant difference was observed between the Lobophora species (Fig. 1). Consequently, A. muricata was selected as a target coral for the identification of allelopathic compounds and the alga L. rosacea was chosen as it is the most common and abundant species in the southwest lagoon of New Caledonia, allowing collection of enough material for subsequent analytical identification of purified allelopathic compounds.

Bioassay-guided fractionation

The L. rosacea extract was fractionated by VLC into five fractions of contrasting polarity. Out of the five fractions tested against the coral A. muricata, the less polar ones (F3 to F5) caused significant visual bleaching and suppression of photosynthetic efficiency relative to controls (Fig. 2), with a decrease of the photosynthetic efficiency of ca. 50% for F3 and F4 and of 70% for F5. The most polar fractions (F1 and F2) significantly suppressed coral photosynthetic efficiency (25% decrease) but less than F3–F5. F4 and F5 displayed very similar HPLC-DAD-ELSD-MS profiles and consequently only F3 and F4 were chemically studied.

A first fractionation of F3 by reversed phase HPLC resulted in 14 sub-fractions named F3P1 to F3P14. Because most of them were still identified as mixtures of compounds by 1H NMR, the most bioactive sub-fractions were further purified to identify compounds responsible for the bioactivity. Therefore, the final purification of F3P13, F3P10 and F3P11 led to the pure compounds 1 (F3P13a), 2 (F3P10a) and 3 (F3P11b) respectively (Fig. 3). The structure of the chemical components of the other sub-fractions was not identified due to the low amount available or complexity of the mixture. Reversed phase HPLC fractionation of F4 resulted in five sub-fractions (F4P1-F4P5) from which no pure compound was identified.

Subfractions and pure compounds caused contrasting effects, with ca. 80% of them causing significant bleaching and suppression of photosynthetic efficiency relative to controls (Fig. 4). The suppression of photosynthetic efficiency ranged from ca. 40 to 80%, relative to the coral effective quantum yield baseline, depending on the sub-fractions. Based on the Tukey HSD post hoc test results, six significantly different groups of allelopathic sub-fractions or pure compounds stood out. Three allelopathic compounds were selected for structure identification, as they were considered sufficiently pure.

Structure identification of compounds 1–3

Compound 1 was isolated as colorless oil and its molecular formula was proposed as C21H31ClO by HRESIMS analysis ([M + NH4]+ at m/z 352.2407 and 354.2382 with isotopic ratio 3:1). The 1H NMR analysis started with a terminal vinyl group at δH 5.34 (dt, H-1a), 5.21 (dt, H-1b) and 6.02 (ddd, H-2) which was COSY coupled to a deshielded methine at δH 4.38 (ddt, H-3) (Table 2). Even if we first suspected the presence of a secondary alcohol at this position, the chemical shift of the corresponding carbon was more shielded than expected at δC 67.8 (C-3) for an allylic alcohol. In agreement with MS data, we then deduced the presence of a chlorine atom at this position which was COSY correlated to a oxygenated methine (δH 3.70 ddd, H-4; δC 75.2, C-4). The spin coupled system was then extended to an ABXM system at δH 2.49 (H-5a) and 2.25 (H-5b) which was further coupled to an alternate polyunsaturated carbon chain composed of four double bonds separated by three methylenes. The configurations of the double bonds were assigned as Z by interpretation of the chemical shifts of allylic carbons. All these connections were later confirmed using HSQC and HMBC spectra. The other end of the compound was deduced to be composed of a second terminal vinylic system coupled to the polyunsaturated core trough three COSY correlated methylene units. Unfortunately no similar allylic chlorohydrine was found in the literature that could allow us to conclude on the relative configuration of 1. We then decided to compare the 13C NMR experimental values with the calculated values obtained on the most stable conformers of the like and unlike diasteroisomers. Working on the most stable conformer, the Mean Absolute Error (MAE) was found to be lower for the unlike configuration (Fig. 5).

Table 2 1H (500 MHz) and 13C NMR (125 MHz) chemical shifts (in ppm) for compounds 1–3 in CD3OD.
Figure 5
figure 5

Mean Absolute Errors (MAE) and Corrected Mean Absolute Errors (CMAE) obtained between the 13C NMR experimental and theoretical values for the two possible diasteroisomers of compounds 1 and 2.

For 2, the isotopic pattern of the HRESIMS spectrum evidenced the absence of a chlorine atom in this molecule and the molecular peak at m/z 334.2744 ([M + NH4]+) suggests the replacement of this atom by an alcohol. Inspection of the 1H and 13C NMR spectra allowed us to localize the structural changes in the vicinity of the first vinylic system. Indeed, the methine signals at δH 4.38 (ddt, H-3) and δC 67.8 (C-3) in 1 were replaced by signals at δH 3.94 (H-3) and δC 76.6 (C-3) that are reminiscent of an allylic secondary alcohol. Therefore, the chlorine atom placed at C-3 in 1 was replaced by a second alcohol in 2 at this position. The relative configuration of compound 2 was deduced to be unlike applying the same method as for 1 (Fig. 5). In this case, hydrogen bonds between the two vicinal alcohols render the gauche conformer more stable than the anti obtained for 1. Both compounds may be produced by an anti opening of a common epoxide intermediate with water or a chloride ion.

The HR-(+)ESIMS data obtained for compound 3 with a molecular peak at m/z 336.2895 ([M + NH4]+) suggested that this natural product corresponds to a dihydrogenated derivative of 2. The location of the reduced double bond was unambiguously deduced from 1H NMR data that showed the lack of a terminal vinylic system. The appearance of a methyl at δH 0.97 (t, H-1) definitely placed the new ethyl group at the beginning of the chain. We assume the same relative configuration for this compound as those previously proposed for 1 and 2, being linked biosynthetically. The low amounts of compounds isolated prevented any attempts to assign their absolute configuration at C-3 and C-4.


Proliferation of Lobophora in coral reef environments has repeatedly caused concern among biologists16,28. There is, however, considerable uncertainty regarding the causes underlying such proliferations as well as of the threat that Lobophora poses to corals. In addition, given the recent progress in understanding species-level diversity in the genus, it is not known whether all or only a subset of Lobophora species compete with corals for space. Our survey of Lobophora – coral associations in the southwest lagoon of New Caledonia demonstrates that not all species of Lobophora associate with corals. Out of eight Lobophora species, three never associated with a coral, but instead grew attached to scattered hard substrate in seagrass beds, shallow wave-washed habitats or coral rubble. Nevertheless, perhaps some interactions may have been detected with greater observations. The other five species were associated with living coral colonies, but grew at the dead bases adopting procumbent to decumbent forms (e.g. L. dimorpha, L. undulata, L. hederacea, L. monticola), or a fasciculate morphology niched within coral branches such as L. rosacea. The latter species is also the most commonly encountered, being observed in 42% of the transects. Most Lobophora species, however, were only observed in 10 to 20% of the transects. Even then, these numbers tend to overestimate the prevalence of Lobophora on the entire reef since the sites where the transects were laid out were precisely those locations where Lobophora – coral interactions were most conspicuous during initial surveys. Per transect, the presence of Lobophora never surmounted 25%. Acropora species were clearly the preferred partner, but all but one Lobophora species displayed a broader range of hosts. Corals associated with Lobophora did not present traces of bleaching (Fig. 6), except in the case of L. hederacea associated with Seriatopora caliendrum.

Based on the ecological niche and the morphological differentiation between Lobophora species we investigated if the species found in direct contact with corals have developed specific allelochemicals capable of impairing corals. Our results demonstrate that all Lobophora species, usually found in contact or not with corals, displayed similar bleaching effects on the tested corals. In other words, naturally found in contact or not, extracts of the eight Lobophora species show similar effects on corals: they are equally capable or not of bleaching specific corals. These results are of significant importance as it implies that species of the genus Lobophora are intrinsically capable of bleaching some corals upon direct contact. In an evolutionary context, this either means that Lobophora has developed: (1) allelopathic compounds targeted towards competing benthic organisms or (2) allelopathy against corals, or other benthic organisms, may be a side-effect (i.e. a secondary unintentional effect) of secondary metabolites with different ecological roles, such as antimicrobial properties (e.g. biofilm deterrents). Recent findings by Rasher and Hay29 showing that the red alga Galaxaura filamentosa uses different compounds to compete with corals versus to resist herbivores would refute the side-effect hypothesis. However, it is unknown at present if a differentiation between allelochemicals and anti-herbivory chemicals is the rule rather than the exception. At least the large fraction of pure or mixed compounds (80% of the isolated compounds from two fractions) that result in a significant suppression of photosynthetic efficiency on corals, would argue against such differentiation.

Among the four coral species tested, A. muricata and M. hirsuta were the most significantly bleached corals. These results indicated a differential susceptibility to Lobophora allelopathy depending on the coral species. In this aspect our results echoed those of Rasher et al.5 who also noticed differential susceptibility across coral species to algal allelopathy. Rasher et al.5 found that A. millepora and P. damicornis were more sensitive to macroalgal allelopathic damage than M. digitata and P. cylindrica. We shared three genera (Acropora, Montipora and Porites) and one species (P. cylindrica) with Rasher et al.5. Also, we had similar results across those genera, although in our case M. hirsuta and P. cylindrica were not damaged at all. P. damicornis, which belongs to the same family as S. pistillata, i.e., Pocilloporidae, was also quite sensitive5. However, Acropora and Montipora, which belong to the same family (Acroporidae), were differentially susceptible in both studies. Partly agreeing with our findings, Lesser et al.30 showed that Acroporids are not as resilient in the face of environmental perturbation compared to other species on the same reef. Nugues and Bak27 also showed that Caribbean corals had differential competitive abilities against Lobophora.

We then proceeded to the isolation and structure identification of the chemicals from L. rosacea exhibiting bleaching properties against A. muricata, the most susceptible coral out of the four tested. Results from the bioassays with the five fractions showed that allelopathy against coral correlates with the polarity of the compounds, with the less polar fractions displaying the highest allelopathic activity. These results concur with the findings of Rasher and Hay8, showing that lipidic extracts from several algal species, including Lobophora variegata, resulted in significant bleaching, while hydrophilic compounds from Chlorodesmis fastigata (Udoteaceae, Chlorophyta) and Galaxaura filamentosa (Galaxauraceae, Rhodophyta) were not active. These results corroborate the importance of direct contact, which is preferable for hydrophobic allelochemicals transfer.

Most of the purified compounds from L. rosacea displayed a significant bleaching effect on A. muricata. The three new C21 polyunsaturated alcohols, named lobophorenols A–C (13) were among the most active fractions and sub-fractions were identified after NMR and MS analyses. These compounds were identified as three new C21 polyunsaturated alcohols. All these compounds may originate after opening of a common epoxide intermediate formed from a polyene. Similar C21 apolar polyenes have been reported only once from the alga Fucus vesiculosus31. It is worth highlighting the presence of a chlorinated analogue 1, which is particularly rare and represent less than 1% of all the secondary metabolites isolated from species of the Phaeophyceae family32,33. Although, we may point out that De Nys et al.8 also isolated halogenated allelochemicals, the presence of the chlorine atom may however not be related to the bleaching properties of the molecule, since both compounds 2 and 3, deprived of this halogen atom, present similar adverse properties. Furthermore, the isolated allelochemicals do not belong to the terpene family of natural products, as somewhat expected from De Nys et al.6 and Rasher and Hay5 but polyunsaturated alcohols. It shows that allelopathy against corals may involve a variety of families of compounds as already reported by Slattery and Lesser11 and strongly supported by the diversity of compounds displaying bleaching properties in this study. The lack of ability to correlate bioactivity with classes of compounds is well known and been discussed numerous times for anti-herbivore compounds, antibiotics, etc.34,35,36. It is worth pointing out that we were expecting to find terpenes, given the richness in terpenoids of the Dictyotaceae family to which Lobophora belongs37. However, much to our surprise this family of compounds was not detected by NMR. Yet, the genus Zonaria, which is sister to Lobophora, did not present terpenes either (authors’ unpublished data).

Lobophora bioactivity against corals does not come as a surprise as in the literature Lobophora extracts (crude, hydrophilic or hydrophobic extracts) and isolated compounds have been shown to display a broad spectrum of activities and in particular antimicrobial (e.g. fungi, bacteria, protozoa) bioactivities e.g.10,38,39. The exact bleaching mechanisms are unaddressed here and could very well be targeting either the polyp or the Symbiodinium. Nonetheless, it is worth mentioning that after two weeks following the bioassays, the surface area which bleached in contact with the patches, recovered their original coloration.

Present field assays would suggest that Lobophora has the potential to chemically impair some coral species by direct contact. Nevertheless, in situ observations indicate that although apparently chemically potent, Lobophora do not or rarely bleach coral hosts in a natural setting (this study). Slattery and Lesser11 also questioned if Lobophora presented allelopathic effects on corals in the Bahamas. Yet, while Lobophora extracts and a purified compound bleached the coral Montastrea cavernosa, contact experiments between Lobophora and the coral did not11. Furthermore, no claim of coral bleaching as a result of contact with Lobophora in natural setting was made by the authors11. Even though it would be tempting to conclude that allelopathy is ecologically important in the competition between Lobophora and corals, there is no strong evidence from field observations. Herbivory on the other hand, clearly appears as an important factor preventing competition to occur11,17,26,28. Therefore, the question remains: what explains the inconsistency between field observations and bioassay experiments? A possible explanation for this discrepancy would be the localization of the bioactive compounds within the endometabolome. Bioassays artificially expose corals to chemicals, a situation that would only occur as a result of abrasion or herbivory under natural conditions. Alternatively, the compounds may be part of the exometabolome, present on the surface of the alga, but external factors (e.g. herbivory) or a defense system by the coral itself may ward off allelopathic interactions, thereby preventing Lobophora from outcompeting corals. Several investigators have demonstrated that bioactive lipids distributed on the surfaces of algae, including Lobophora, were capable of damaging corals5,7,8,40. This forms a strong indication that at least some compounds are present on the algal surface. Given the presence of allopathic compounds, most coral species prevent the overgrowth of crustose Lobophora species owing to a set of defense mechanisms24,27. Additionally, field observations and experiments showed that herbivory is a major factor preventing increase in Lobophora abundance11,26,28. In New Caledonia, only one species of Lobophora, L. hederacea, was observed overgrowing a coral species, Seriatopora caliendrum19. In the latter case, coral overgrowth appears to be possible owing to a combination of factors including the coral vulnerability and the inhibition of grazing19, supporting the important role of coral defense and herbivory in preventing negative allelopathic interactions. In the Great Barrier Reef, Jompa and McCook17 showed that a crustose Lobophora species was capable of overgrowing the coral Porites cylindrica when herbivory was reduced. In damaged reefs, however, coral morbidity and mortality in addition to shifts in herbivory pressure result in whole different setting where macroalgal allelopathy may have harmful effects on corals. Although not yet explored, it is possible that allelopathy in damaged reef may results from the synergetic effects of macroalgal exudates/allelochemicals acting in combination with a number of environmental parameters/stressors such as seawater pH, oxygen depletion and or temperature maxima1.

The role of chemical interactions between macroalgae and corals initially evinced in the early 90s in form of positive allelopathy41, has regained interest only recently, yet this time in form of negative allelopathy8. Most studies on the subject have disclosed deleterious effects (e.g. bleaching, recruitment inhibition) in damaged reefs. The present work, focusing on a healthy reef ecosystem, provided evidence that allelopathic defense is not restricted to Lobophora species that are naturally found in close contact with corals. These findings are important toward our understanding of the importance of allelopathic competition and defense systems versus herbivory in the interaction between macroalgae and corals in reef ecosystems.

Materials and methods

Quantification of Lobophora–corals association

Eight species of Lobophora, commonly encountered in the southwest lagoon of New Caledonia were selected to quantify their association with corals and for the bioassays, i.e. L. abscondita, L. crassa, L. dimorpha, L. hederacea, L. monticola, L. nigrescens, L. undulata and L. rosacea (Fig. 6). 78 belt transects, as described by English et al.42, each 10 m long, were deployed across coral dominated reefs in the southwest lagoon of New Caledonia. Within a belt transect, a 2500 cm2 quadrat (50 × 50 cm) was placed consecutively left and right along a defined line and photographs were taken directly above each quadrat using a Lumix Panasonic digital camera (12 megapixels) mounted on a photoquadrat framer. In each quadrat, the frequency of Lobophora – coral associations was assessed by placing 16 points per quadrat using a stratified random point count method using the software “Coral Point Count with Excel extensions”43. Details of the sampling locations and quantification methods are outlined in Supplementary information. From these data we calculated the percentage of transects in which Lobophora was associated with corals. The average percentage of associations of each species was calculated per transect where the species was observed.

Preparation of the extracts and fractions of Lobophora for bioassays

Algal samples for bioassays were collected by SCUBA in January 2013 in the southwest lagoon of New Caledonia (Supplementary information). Samples were cleaned from epiphytes and stored at −20 °C until freeze-drying. Four coral species were selected as targets of the bioassays, i.e. Acropora muricata (Linnaeus, 1758; Acroporidae), Montipora hirsuta (Nemenzo, 1967; Acroporidae), Stylophora pistillata (Esper, 1797; Pocilloporidae) and Porites cylindrica (Dana, 1846; Poritidae). Algal specimens were identified at species-level using mitochondrial cox3 gene sequences see18. The area of each individual was estimated using the aluminum foil technique44. Then, the specimens were freeze-dried and the dried samples were ground with a mortar and pestle using liquid nitrogen. One gram of ground powder was exhaustively extracted, by adding consecutively three times 10 mL of a 1:1 mixture of dichloromethane/methanol (CH2Cl2/MeOH) (v/v), leaving it 5 min in an ultrasonic bath and 5 min to decant and then retrieving the supernatant liquid (upper phase) using a 100 mm in diameter and 10 μm in porosity qualitative filter paper folded (Whatman, UK). The resulting supernatant was concentrated under vacuum and the extracts were weighted and divided by the algal surface area to obtain a mass of extract per surface area (μ−2).

Crude extracts of L. rosacea were then submitted to fractionation in order to gain information on the polarity of the compounds responsible for the allelopathic activity. The dried extract was resuspended in MeOH/CH2Cl2 (1:1; v/v), mixed with an equal amount of C18 silica powder (Polygoprep® 60-50, Macherey-Nagel, France) and concentrated under vacuum. The resulting powder was deposited on a solid phase extraction (SPE) cartridge (Strata® C18-E, 500 mg/6 mL; Phenomenex, USA) and then fractionated using five solvent mixtures (10 mL for each) of decreasing polarity: H2O, H2O/MeOH (1:1; v/v), MeOH, MeOH/CH2Cl2 (3:1; v/v) and then MeOH/CH2Cl2 (1:1; v/v). The five resulting fractions (F1 to F5) were evaporated under a fume hood during 48h, weighted and divided by the algal surface area to obtain a quantity of fraction per surface area (μ−2).

Isolation and structure identification of specialized metabolites

Since no Lobophora species stood out in terms of bioactivity against A. muricata or any of the other corals (cf. results), L. rosacea was chosen for subsequent analytical identification of purified allelopathic compounds as it is the most common and abundant species in the southwest lagoon of New Caledonia, thus allowing collection of enough material for subsequent analytical identification of purified allelopathic compounds. The biomass (209 g of dry mass) of L. rosacea was exhaustively extracted, by adding consecutively five times MeOH/CH2Cl2 (1:1, v/v; 1.2 L of solvent), leaving it 10 min in an ultrasonic bath and 5 min to decant and then retrieving the supernatant liquid. The resulting extract was concentrated under vacuum to yield a homogeneous dry powder (8.3 g). The extract was then mixed with an equal amount of C18 silica powder (Polygoprep® 60-50) and fractionated by Vacuum Liquid Chromatography (VLC) into five fractions (F1–F5), eluting with the five organic solvents aforementioned for SPE. An additional elution was done with CH2Cl2 in order to ensure exhaustive compounds extraction from the crude extract and was additionally tested as a sixth fraction (F6). The resulting filtrates were evaporated under vacuum, resuspended into MeOH to reach a concentration of 10 mg∙mL−1, filtered through 0.22 μm PTFE syringe filters (Phenomenex, UK) and filled into HPLC vials for subsequent Ultra-High Performance Liquid Chromatography-Diode Array Detection (UHPLC-DAD) analyses and High Performance Liquid Chromatography (HPLC) purification.

According to the results on the ecological activity (cf. next paragraph), F3 and F4 were selected for compounds isolation and purification. The HPLC purification was performed on a Jasco (Groß-Umstadt, Germany) preparative HPLC system (pump PU-2087 plus; diode array detector MD 2018 plus; column thermostat CO 2060 plus; autosampler AS 2055 plus; LC Net II ADC Chromatography Data Solutions; sample injection loop: 250 μL) on a phenyl-hexyl reversed phase column (XSelect CSH™, 5 μm, 19 × 250 mm; Waters, France), using for F3 an isocratic elution mode [acetonitrile (CH3CN) + 0.1% trifluoroacetic acid (TFA)/H2O + 0.1% TFA; 69/31, v/v] and a flow rate of 10 mL/min. Fourteen sub-fractions (from F3P1 to F3P14) were obtained. Fraction F4 was fractionated on the same column with a CH3CN/H2O + 0.1% TFA gradient on a 30 min run (0–5 min: 90% CH3CN; 5–10 min: 90 at 100% CH3CN, 10–25 min: 100% CH3CN) at 10 mL/min, leading to five sub-fractions (F4P1 to F4P5). The purification of compounds from four sub-fractions of F3 (F3P10, F3P11, F3P13 and F3P14) were performed on a C18 semi-preparative column (XSelect CSH™ C18, 5 μm, OBD, 19 × 250 mm; Waters, France) with a CH3CN/H2O + 0,1% TFA gradient (UV detection: 210 nm, flow rate: 10 mL/min).

Among all the fractions and sub-fractions only the three major, pure and bioactive compounds 13, corresponding to fractions F3P13a (18.4 mg), F3P10a (3.8 mg) and F3P11b (3 mg) respectively, were identified on the basis of NMR and MS data.

NMR analyses were performed in CD3OD on a Bruker Avance 500 spectrometer using signals of the residual peaks of the solvent for calibration of the chemical shifts in ppm (δH 3.31 for 1H NMR and δC 49.0 for 13C NMR). LC-DAD-ELSD-ESI/MSn analyses were carried out on a LaChrom Elite HPLC (VWR-Hitachi) composed of a L-2130 quaternary pump, a L-2200 autosampler and a L-2300 column oven. Detection was performed with a L2455 DAD and an ELSD (Chromachem model, Eurosep) coupled to an Esquire 6000 spectrometer. UHPLC-HRMS were performed on a UHPLC U3000 (Dionex) coupled to a QqToF Impact II (Bruker).

In situ allelochemical assays

Field experiments, conducted in situ were designed to keep the coral under natural field conditions, thus limiting pre-experimental stress usually resulting from cutting, gluing and transplantation. The bioassays were conducted in Sainte Marie Bay (22° 17.863′ S, 166° 28.898′ E) with three of the coral genera, i.e. Acropora muricata, Porites cylindrica and Montipora hirsuta and on genus in Maitre Islet Reef for Stylophora pistillata (22° 20.446′ S, 166° 24.108′ E). A series of three bioassay experiments were successively performed. The first experiment evaluated the bioactivity of the crude extract of the Lobophora species previously selected (L. abscondita, L. crassa, L. dimorpha, L. hederacea, L. monticola, L. nigrescens, L. undulata and L. rosacea) on four coral species (Acropora muricata, Porites cylindrica, Stylophora pistillata and Montipora hirsuta). The second experiment tested the bioactivity of the five fractions obtained from the extracts of L. rosacea on A. muricata. The final experiment tested the bioactivity of the sub-fractions and compounds from two of the most bioactive fractions of L. rosacea identified in the previous experiment (F3 and F4). All bioassay experiments were performed in situ directly on coral colonies at approximately natural concentration (i.e. concentration per surface area previously estimated), the latter being critical for bioassays assessing allelopathic interactions. Thereto, we determined the amount of crude extracts, fractions, sub-fractions and pure compounds per unit of algal surface area (i.e. 1 cm2) and reported it to the surface of the agarose patch applied on the coral (i.e. 2 cm2).

A replicate was defined by one colony of coral on which all the extracts, fractions or sub-fractions (including in some cases pure isolated compounds) were tested. A total of 10 replicates were implemented. The methodology was adapted from Rasher and Hay8. The chemical samples (crude extracts, fractions, sub-fractions or pure compounds) were resuspended in 1 mL MeOH and added at natural concentration into a 4% agarose gel (Conda Pronadisa, Spain). The mix chemical sample/agarose was poured into a polyvinyl chloride mold, composed of 10 times 2-cm2 wells. Before that, tulle bands, of 20 × 2 cm, were disposed at the bottom of the wells onto which the gel mixture will adhere while gelifying. The strips were prepared the day before field application and refrigerated until then at 5 °C. They were applied onto the coral by knotting the tulle bands to the branches and removed after 24 h of exposure. Agarose strips with and without MeOH were additionally made as controls, to ensure the non-effect of either the agarose strips itself or the solvent on the coral. Gel strips were applied on the corals between 09:00 and 11:00 AM.

Coral photosynthesis measurements

Pulse Amplitude Modulated (PAM) fluorometry measurements were performed with a Diving-PAM (Walz) right after removal of the strips. PAM fluorometry measures the photosynthetic efficiency of photosystem II within the endosymbiotic Symbiodinium spp. that may be used as a quantitative measure of photo-inactivation during coral bleaching45. PAM fluorometry values of healthy corals are ranging between 0.5 to 0.8, depending on the coral species and time of the day. Values between 0 to 0.2 are indicative of severe bleaching or mortality46. As outlined in Rasher and Hay8 PAM fluorometry measurements were performed where the strips were applied and 5-cm next to it, as a spatial control to have a coral health baseline for comparison.

Statistical analyses

Normality of distribution of the coral responses for all the bioassay experiments was tested with the normality Shapiro-Wilk test. If the responses violated parametric assumptions, coral responses were evaluated using the Kruskal-Wallis H test followed by the Tukey honestly significant difference (HSD) post hoc comparisons test for significant Kruskall-Wallis findings. If the data respected the parametric assumptions, a one-way ANOVA was performed followed by the Tukey post hoc HSD test for significant ANOVA findings. Statistical analyses were performed using the computing environment R47.

Additional Information

How to cite this article: Vieira, C. et al. Allelopathic interactions between the brown algal genus Lobophora (Dictyotales, Phaeophyceae) and scleractinian corals. Sci. Rep. 6, 18637; doi: 10.1038/srep18637 (2016).