Novel Adaptive Photosynthetic Characteristics of Mesophotic Symbiotic Microalgae within the Reef-Building Coral, Stylophora pistillata

Introduction

Scleractinian corals build the framework of the world's tropical reefs and their growth relies primarily on photosynthetic dinoflagellate endosymbionts from the genus Symbiodinium (Jones et al., 1998). These photosymbionts reside within the corals endoderm and produce photosynthates that are translocated to the host (Muscatine et al., 1975; Falkowski and Dubinsky, 1981). While shallow reefs have been extensively studied, the deeper mesophotic environment (>30 m) has been much less examined due to difficulty to access, such as the need for technical diving or remotely operated vehicles. Light intensity decays exponentially with depth (Gordon, 1989) and therefore, the mesophotic reef environment, known as the “twilight zone,” is characterized by light fluxes that vary seasonally between 5 and 100 μmol photons m⁻² s⁻¹. This dim mesophotic setting, therefore, receives 15–300 times less of a photon flux than shallow reef counterparts ~1500 μmol photons m⁻² s⁻¹ (Levy et al., 2003). The low light flux in the mesophotic region impacts corals photosynthetic and calcification rates and limits their vertical distribution throughout the photic zone (Wells, 1957; Dubinsky et al., 1984; Franklin et al., 1996; Jones et al., 1998). In addition, deeper reefs receive narrower spectra, primarily blue light spectra centered at 467 nm, than the wider spectral range of shallow waters (Dishon et al., 2013). In mesophotic, low-light conditions, corals have been shown to shift their energetic budget to heterotrophic predation (Muscatine and Kaplan, 1994; Einbinder et al., 2009). Symbiodinium has also been shown to acclimate to low-light regimes (Cohen and Dubinsky, 2015). The current understanding is that two mechanisms are involved: (1) an increase in the effective antenna size—antenna pigments per photosynthetic unit (PSU) (Falkowski and Dubinsky, 1981; Franklin et al., 1996) and (2) an increase of photosynthetic units (PSU) per cell (Chang et al., 1983; Prézelin, 1987; Iglesias-Prieto and Trench, 1997; Pratchett et al., 2008; Hennige et al., 2009; Hutchings et al., 2009; Lesser et al., 2010). However, there have also been studies that have reported no significant changes in the Symbiodinium chlorophyll content at depths below 25 m (Titlyanov et al., 2002; Mass et al., 2007; Lesser et al., 2010).

In shallow high light conditions thermal dissipation, Non photochemical Quenching (NPQ) provides a mechanism that protects Symbiodinium photosynthetic apparatus from excess photosynthetic active radiation (PAR) damage (Hoegh-Guldberg and Jones, 1999). Dinoflagellates contain two types of photosynthetic antenna: A membrane bound intrinsic antenna–acpPC (Chl a-Chl c2-peridinin protein complex) as shown in Figure 1 (Niedzwiedzki et al., 2014); and a soluble membrane complex PCP (peridinin-Chl a protein). NPQ was shown to be associated with the conversion of diadinoxanthin to diatoxanthin (Brown, 1997). Xanthophyll epoxidation and de-epoxidation decreases photon flux to PSII reaction centers and thus prevents over reduction of the quinone acceptors by reducing the functional absorption cross-section of PSII reaction centers (σPSII). In corals, the quencher in the NPQ processes was suggested to reside in the apcCP antenna (Iglesias-Prieto and Trench, 1997; Kanazawa et al., 2014).

FIGURE 1

Figure 1. Schematic representation of the photosynthetic apparatus in Symbiodinium spp.

NPQ has a finite capacity and may reach saturation while excess electrons continue to reduce the electron transport chain (Brown et al., 1999; Dustan, 1999; Smith et al., 2005). Alternative sinks for electrons, other than CO₂ assimilation, may provide additional protection mechanisms to help prevent over reduction at high light intensities. PSI can directly reduce O₂ via the Mehler reaction to produce superoxide radicals that are rapidly converted within the chloroplast to hydrogen peroxide by superoxide dismutase (Jones et al., 1998). Hydrogen peroxide is then detoxified to produce water by ascorbate peroxidase, which oxidizes ascorbate to monodehydroascorbate (Asada, 1999).

While there is a wealth of information on short-term processes of light regime change acclimation mechanisms, long-term processes accounting for the diversity of both symbionts and hosts have only recently been explored (Iglesias-Prieto et al., 2004; Bongaerts et al., 2011, 2013; Cooper et al., 2011; van Oppen et al., 2011; Brazeau et al., 2013; Nir et al., 2014). Most indicate distinct deep and shallow symbionts types, with a few generalist types (Lesser et al., 2010).

In this study, we examined Stylophora pistillata at 65 and 3 m, as well as those slowly transplanted from shallow to deep, in an attempt to elucidate what long-term acclimation or adaptation processes photosynthetic dinoflagellates possess in high and low light environments. We are also investigated potential mechanisms of efficient energy transfer at mesophotic depths.

Materials and Methods

In order to investigate the photosynthetic characteristics of mesophotic and shallow corals we conducted a series of analyses on intact corals and their isolated Symbiodinium and determined their net and gross photosynthesis rates as a function of irradiance (PI), PSII quantum yield, non-photochemical quenching (NPQ) parameters, chlorophyll fluorescence emission spectra and PSI activity.

Sample Collection and Preparation for Analysis

Coral samples were collected in the Northern Red Sea (29⋅30′N, 34⋅56′E) from a gradient of 3 to 65 m along the fore reef slope. Branches of the hermatypic corals S. pistillata (wide depth range, 0–70 m) (Fricke and Schuhmacher, 1983) were collected from their natural habitats using closed circuit Trimix rebreather systems (Megalodon™). To distinguish between adaptive or acclimation responses, over almost 4 years (June 2004-April 2008), we gradually transferred (5 m/2 weeks) mesophotic S. pistillata from a depth of 65 to 5 m, and shallow S. pistillata from 5 m to a final depth of 65 m. The corals then remained at either depth until the conclusion of the experiment when they were removed for analysis. Samples were collected in light-proof black bags and brought to the incubation area where light intensity was controlled to duplicate source depths. The collection was conducted under permit number 31944 from the Israel Nature and Parks Authority. Samples were held for less than 18 h, and then transferred for further analysis.

Fluorescence Parameters (PSII)

Chlorophyll fluorescence parameters were measured using a Fluorescence Induction and Relaxation (FIRe) fluorometer (Satlantic) and a PAM imaging system fluorometer (Walz, GmbH, Effeltrich, Germany). The corals were dark-adapted for 30 min prior to measurements. A single saturating pulse (4000 μmol photons m⁻² s⁻¹, white-light, 500 ms for the PAM and 10,000 μmol photons m⁻² s⁻¹, blue-light, 80 μs for the FIRe) was triggered, and PSII maximal fluorescence (F_m) was measured.

NPQ was calculated as described in Schreiber (2004) where NPQ = (F_m − ${\text{F}}_{\text{m}}^{\prime }$)/${\text{F}}_{\text{m}}^{\prime }$. ${\text{F}}_{\text{m}}^{\prime }$ was obtained after steady state fluorescence was achieved under an actinic light intensity of (0–1000 μmol photons m⁻² s⁻¹ for the PAM and a 1000 μmol photons m⁻² s⁻¹ (Schott KL2500LCD) for the FIRe measurement.

Oxygen Evolution and Consumption (Net and Gross Photosynthesis)

A quadrupole mass spectrometer (Balzers QMG 421) with a membrane inlet (MIMS) was used to measure dissolved gas in a climate and light controlled chaimber (3.3 ml volume). Simultaneous measurements of argon and mass 14 concentration were used to assess the stability of the system as described in Tchernov et al. (1997, 2001). The action medium consisted of artificial sea water (ASW) pH 8.2 with 2 mM total dissolved inorganic carbon.

PSI Relative Function through Oxygen Consumption

Fresh symbionts were extracted from coral fragments and placed in the action medium that consisted of ASW pH 8.2 with 2 mM total dissolved inorganic carbon. The algae were incubated in the dark in the presence of 10–5 M (3-(3,4-dichlorophenyl)-1,1-dimethylurea) DCMU (D2425 Sigma) for 20 min. When there was no detectable oxygen evolution under illumination at saturating light intensity (400 μmol photons m⁻² s⁻¹) lights were turned off and 30 μM (sodium 2,6-dichloroindophenol) DCIP, (33125 Sigma), 0.3 mM sodium ascorbate (A7631 Sigma), and 70 μM methyl viologen (856177 Sigma) were added (Kyle et al., 1984). The FIZ were transferred into a temperature controlled (26⋅C ± 0.5) MIMS chamber. Upon illumination, oxygen was monitored on line using the MIMS as described in Tchernov et al. (1997, 2001). The rate of oxygen consumption was normalized to chlorophyll concentration.

Pigments Analysis

Coral fragments (2 cm) were airbrushed and purified using the same protocol as Stochaj and Grossman (1997) and resuspended in 100% methanol. After ensuring identical samples (chlorophyll concentration), we followed the protocol of Rogers and Marcovich (2007) for pigment HPLC analysis. The samples were incubated in 4⋅C for 2 h and were vortexed for 2 min every 30 min. The samples were incubated overnight in the presence of ammonium acetate (pH 7.2, −20⋅C). The mixture was vortexed again and centrifuged (14,000 rpm, 4⋅C, 20 min). The pellet was discarded and the supernatant was injected into a HPLC equipped with a reverse-phased column (Spherisorb ODS-2 column -silica 5 μm, 3.2 mm × 250 mm (Phenomenex^®) analysis.

Photosynthesis/Irradiance Measurements

Coral fragments were airbrushed to release the Symbiodinium symbionts, cleaned via triple washing with 0.2 μm filtered seawater and then placed in a temperature-controlled chamber (2.8 ml) at 26⋅C in artificial seawater (pH 8.2) supplemented with 2 mM dissolved inorganic carbon (S5761 Sigma). For illumination, Schott^© KL2500LCD unit with two optic fibers were connected to special optic ports to the chamber. The various chemicals supplied to the cell suspension were introduced via a top injection port. In order to measure respiration during light photosynthesis, isotopic labeling oxygen method incorporated as in Bender et al. (1987). The sample was spiked with ${\text{H}}_2^{18}$O, incubated in light, and measured for labeled oxygen dilution. Detection was performed by a Membrane Inlet Mass Spectrometry (MIMS) apparatus. As all the labeled O₂ is contained in a single well-defined dissolved gas phase and the ambient O₂ pool assumed to be much larger, only a negligible amount of O₂ will be recycled by respiration during the incubation. For normalization, chlorophyll was extracted using 90% acetone, as in Jeffrey and Humphrey (1975). PSI activity values were calculated from the initial slopes.

Phylogenetic Analysis

Phylogenetic analysis of the ITS2 sequences (316 bp) using parsimony (PAUP 4) algorithm carried out with 26 representative sequences of seven clades and three sequences obtained from this study (deep, shallow and transplant, Supplementary Table 1). The ITS2 sequence of Gymnodinium aureolum was used as an out-group. Values (%) of 500 bootstrap replicates are given at branching points for parsimony/distance analyses. Corals from shallow water and transplant present zooxanthellae from clade A while the symbiont of the deep-water cluster with clade c.

Results

Dynamics of the Photosynthetic Light Response

For the study of the dynamics of the photosynthetic apparatus we used four groups of corals: shallow and mesophotic coral fragments and two depth transplants groups (3 and 65 m, Figure 2). NPQ activity was measured in S. pistillata (3 and 65 m), and was up to five times higher in shallow corals than in the mesophotic corals (Figure 3 and Table 1).

FIGURE 2

Figure 2. Example of Stylophora pistillata from shallow and mesophotic environments. (A) 3 m; (B) 65 m.

FIGURE 3

Figure 3. NPQ analysis of mesophotic, shallow and transplanted corals. Measurements were performed using PAM imaging system. The top panel presents a false color image of the coral fragments. The values indicated are Fv/Fm average calculated from three independent fragments. The bottom panel presents NPQ values as a function of incident light intensity for the three coral fragment groups. Mesophotic corals symbionts lose a small fraction of excessive absorbed energy to photoprotective measures.

TABLE 1

Table 1. Photosynthetic parameters.

The transfer of 65 m mesophotic Stylophora colonies to shallow 5 m environments resulted in lethal responses, despite a slow assent rate (5 m every 2 weeks). This is in agreement with (Baker, 2003) that indicates mortality of deeper colonies upon ascending transplant experiments. Yet, the transfer of shallow corals to the mesophotic region was successful. For shallow corals transplanted to 65 m, a marked difference in NPQ from the mesophotic corals was observed, indicating a shallow-type response (Figure 3). Phylogenetic sampling showed that transplanted corals retain their original Symbiodinium type. This differed from the non-transplanted corals as well as from control corals that were transplanted laterally along the same depth (Supplementary Figure 1). The different symbiont population discovered at mesophotic depths hints that it diverged from shallow population to provide an adaptive advantage. These results prompted us to take a closer mechanistic look at the differences in the function of the photosynthetic apparatus.

Organization of the Photosynthetic Apparatus

The rates of oxygen production and uptake reactions were studied in detail using the Membrane Inlet Mass-Spectrometry technique (MIMS). Using MIMS determined that S. pistillata from 65 m performed below their photosynthetic compensation point (where oxygen uptake and production rates are equal) at the natural ambient low-light intensities (Figure 4). Shallow corals performed close to their photosynthetic P_max in their ambient high-light conditions. The P_max of mesophotic corals from 65 m was ~1.6-fold lower than that of their shallow counterparts (Table 1), a finding in agreement with (Falkowski and Dubinsky, 1981). Mesophotic corals did not exhibit a decrease in oxygen production when subjected to high-light intensities of nearly two orders of magnitude higher than their natural light environment (Figure 4). The relatively low P_max is in accordance with the prevalent shade-adapted response in photosynthetic organisms. Mesophotic corals displayed a low initial rate constant (α), comparable to shallow corals (Table 1). This differs from the typical response of shade-adapted species that exhibit lower P_max at low-light intensities and retain high photosynthetic efficiency (α), due to an increased antenna size (Björkman, 1966).

FIGURE 4

Figure 4. Photosynthesis-Irradiance measurements of the initial mesophotic (65 m) and shallow (3 m) corals Symbiodinium sp. depicting (A) Net Photosynthesis and (B) Gross photosynthesis. Mesophotic symbionts do not experience dynamic photoinhibition at shallow light intensities.

Using the Fluorescence Induction and Relaxation (FIRe) approach (Kolber et al., 1998), we found that mesophotic PSII traps energy better than shallow PSII; and its variable fluorescence magnitude is higher than the shallow symbionts (Table 1). However, mesophotic Q_A-reoxidation time constant (τ) was slightly slower than the shallow PSU constant (Table 1,) and the absorption cross-section (σP₆₈₀) was significantly lower (Table 1), implying an overall smaller PSU size.

The photosynthetic pigments concentration ratios were obtained via High Performance Liquid Chromatography (HPLC) (Table 1). Mesophotic Symbiodinium contain substantially less antenna pigments on a chlorophyll basis. The percent decrease was greater for Chlorophyll C then for Peridinin (34 and 18%, respectively). This data suggests a shift to smaller antenna size in mesophotic corals, with a composition favoring membrane anchored PCP over membrane embedded apcCP. Partial electron transport measurements of freshly isolated Symbiodinium (FIZ) were performed using a membrane inlet mass-spectrometer (MIMS). A ratio of 2.7 ± 0.7 in PSI activity was recorded between shallow and mesophotic samples (Table 1), suggesting reduced PSI content in mesophotic samples.

Energy Transfer between Antenna and Reaction Centres

Fluorescence rise kinetics in the presence of DCMU was measured to investigate the dynamics of PSII and antenna energy transfer processes. In the presence of DCMU, blocking electron transport at the Q_B site, fluorescence emission kinetics reflects the interplay of antenna excitation migration and subsequent PSII charge separation. Fluorescence rise kinetics of deep corals was strongly sigmoidal as compared to the shallow corals (Figure 5). The sigmoidal nature of the mesophotic corals fluorescence kinetics extended their rise time compared to shallow corals, the difference being most pronounced under low light intensities (Figure 5).

FIGURE 5

Figure 5. Chlorophyll fluorescence rise kinetics. The actinic light was turned on at 10⁻³ s. (A) Shallow corals (3 m) are represented by open symbols, mesophotic corals (65 m) depth are represented by closed symbols. Curves fitted to a sigmoid trandline (R² > 0.97 for all curves). The fluorescence rise half time, extracted from the sigmoidal fit, for deep and shallow corals is plotted as a function of the actinic light intensity. Standard deviation values calculated from three samples for each depth. Values represent the time for the signal to reach 50% of its maximum excitation. (B) An example for the raw data where 220 μmole photons m⁻² s⁻¹ red light excitation (620 nm) was used.

Discussion

The combination of static depth-related chlorophyll content per cell (Mass et al., 2007) with a distinct decrease in PSI activity, and enhanced sigmoidal fluorescence rise kinetics suggests a distinct organization of the photosynthetic apparatus of mesophotic corals (Figure 6). In the photosynthetic apparatus, PSI supports the linear electron transport process leading to the generation of ATP and NADPH and cyclic electron transport processes affecting ATP/NADPH ratios. Cyclic processes are considered as means for adjusting the redox poise and as a protective mechanism preventing excess excitation induced damages (Munekage et al., 2004; Nawrocki et al., 2015). At low light intensities such protection is not required.

FIGURE 6

Figure 6. Schematic model of the organization of the photosynthetic apparatus in shallow (top) and mesophotic/deep (bottom) corals.

The theoretical limit (Falkowski and Dubinsky, 1981) for enhancing light absorption through an increase in the effective antenna cross section was calculated to be 1650 ± 175 Chl a per P₇₀₀ (Falkowski and Dubinsky, 1981) at a depth equivalent to 30 m (where light intensity is equated to the light intensity at the depth the coral was extracted). This mechanism, therefore, cannot be efficient in the deeper mesophotic reef environment. An increase in PSU per cell may be effective for low-light acclimation, as described by several groups (Chang et al., 1983; Prézelin, 1987; Iglesias-Prieto and Trench, 1997; Hutchings et al., 2009). In this study, as well as in previous work (Mass et al., 2007) evidence of an acclimation pathway mechanism was not found at mesophotic depths.

PSII's shallow energetic trap allows exactions to be distributed between closed and open reaction centers. This creates an efficient low-light energy transfer scheme that is displayed in our data as a sigmoid fluorescence rise kinetics curve, shown only in the deep corals. The sigmoidal fluorescence rise kinetics that we observed in mesophotic corals is an indication of energy transfer between photosynthetic units (Trissl et al., 1993; Lavergne and Trissl, 1995). Under low-light intensities, this energy transfer increases photosynthetic quantum efficiency (Joliot and Joliot, 1964, 2003). The lower PSI content and the shift from a membrane embedded to a membrane-attached light harvesting system can facilitate this type of cooperativity. We postulate that at mesophotic depths, a community of adapted Symbiodinium spp. occupies most of the corals and they utilize a unique adaptation to the “twilight” conditions by shifting their light harvesting to a PSII based system, where PSII is structured near PSI, with additional PCP soluble antenna also trapping light that is funneled to the PSI reaction center. Our genetic data suggest that mesophotic S. pistillata have one species of symbionts that maintain these traits. Shallow corals and those transplanted from shallow to deep kept their shallow traits, such as high NPQ that serves as a line of defense against photoinhibitory damage (Papageorgiou and Govindjee, 1968; Takahashi et al., 2008). These finding points to an adaptive mechanism in mesophotic corals, rather than the previously noted acclimation strategies. Other species of mesophotic corals and other photosynthetic organisms living in perpetually low-light environments should be examined to determine if they also share this novel, energy efficient low-light photosynthesis strategy.

Author Contributions

Planned the study: SE, DG, ES, OL, NK, and DT. Performed Pigments Analysis: SE, ES, OL, NK, and DT. Performed Photosynthesis/Irradiance Measurements: SE, ES, OL, NK, and DT. Wrote the manuscript: SE, DG, ES, OL, NK, and DT.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer GE declared a shared affiliation, though no other collaboration, with one of the authors OL to the handling Editor, who ensured that the process nevertheless met the standards of a fair and objective review.

Acknowledgments

We thank K. Zendbank for assisting in molecular work and the Interuniversity Institute for Marine Sciences and staff in Eilat, Israel, for contributing to field studies. We greatly thank E. Brokovitch and O. Ben-Sharput for participating in the technical dives. The research was supported by the Israel Science Foundation grant # 981/05 to DT, the Bundesministerium für Bildung und Forschung, Germany, grant # 1923–1300 to DT and the US National Science Foundation grant # 0920572 and 1556213 to DG.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fmars.2016.00195

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