Reactive oxygen production induced by near-infrared radiation in three strains of the Chl d-containing cyanobacterium Acaryochloris marina

Cyanobacteria in the genus Acaryochloris have largely exchanged Chl a with Chl d, enabling them to harvest near-infrared-radiation (NIR) for oxygenic photosynthesis, a biochemical pathway prone to generate reactive oxygen species (ROS). In this study, ROS production under different light conditions was quantified in three Acaryochloris strains (MBIC11017, HICR111A and the novel strain CRS) using a real-time ethylene detector in conjunction with addition of 2-keto-4-thiomethylbutyric acid, a substrate that is converted to ethylene when reacting with certain types of ROS. In all strains, NIR was found to generate less ROS than visible light (VIS). More ROS was generated if strains MBIC11017 and HICR111A were adapted to NIR and then exposed to VIS, while strain CRS demonstrated the opposite behavior. This is the very first study of ROS generation and suggests that Acaryochloris can avoid a considerable amount of light-induced stress by using NIR instead of VIS for its photosynthesis, adding further evolutionary arguments to their widespread appearance.

Most oxyphototrophs use visible light (VIS, 400-700 nm) for chlorophyll (Chl) a-driven photosynthesis, while cyanobacteria in the genus Acaryochloris largely employ Chl d, thereby enabling them to use nearinfrared radiation (NIR, >700 nm) for oxygenic photosynthesis 1,2 . Two of the strains are well described in their growth and photopigment composition: The type strain Acaryochloris marina MBIC11017 was isolated from the didemnid ascidian Lissoclinum patella from coral reefs habitats in Palau 2,3 and was later genome sequenced 4 . The other strain, HICR111A, originates from swipes of coral substrate collected on Heron Island, Australia and was also genome sequenced 5 . Since its first discovery, other Acaryochloris strains have been obtained from Japanese macroalgae (strain Awaji 6 ), from surfaces in a hypertrophic lake in the US (strain CCMEE5410 7 ), and most recently from Australian mangroves 8 (strain MPGRS1) and stromatolites in Shark Bay, Western Australia 9 (ssball1).
The light microenvironment in natural habitats occupied by Acaryochloris spp. has a high contribution of NIR relative to visible light 10-12 and such habitats appear to create similar niche differentiation with bacteria carrying specialized photopigments such as Chl d/f or bacteriochlorophylls 10,13 . The notion of a global distribution of Chl d and cyanobacteria in the genus Acaryochloris 11,14 further reinforces the need to obtain information on the photobiology of Chl d-containing oxyphototrophs. Understanding the adaptive mechanisms in oxyphototrophs capable of using wavelengths beyond VIS is of interest as it provides information concerning the usability, stress levels and limitations associated with NIR-driven oxygenic photosynthesis.
Of all biological pathways, photosynthetic electron transport is particularly prone to produce reactive oxygen species (ROS) due to the very high (positive) redox potential of the primary donor of photosystem II, needed to oxidize water, and the low redox potential of the primary electron acceptor of photosystem I, needed to reduce ferredoxin; here, singlet oxygen ( 1 O 2 ), is produced by PSII and superoxide anions ( -O 2 )/hydrogen peroxide (H 2 O 2 ) in the Mehler, ascorbate peroxidase (MAP) pathway of PSI [15][16][17] . ROS encompasses the production of singlet oxygen, superoxide anions, hydrogen peroxide and hydroxyl radicals (OH . ), all of which are derived through the local energization of O 2 . If not properly quenched by protective mechanisms, ROS can damage proteins,

Changes from Version 1
The manuscript has been edited with the help of the reviewer's comments and should now address the most critical points.
We have augmented parts of the discussion section, which now provides additional information concerning the potential role of carotenoids in the quenching of ROS. A sentence was added to clarify which radicals are detected with the KMBA assay. Additionally, we have tried to tone down our claims of the significance of this study and acknowledged the fact that some measurements could be uncertain due to lack of replication or biological variation. All minor points given by the three referees were addressed. We hope that the changes made are in agreement with the reviewers comments and improve the manuscript.

See referee reports
DNA and other cellular macromolecules, and this damage can ultimately lead to cell death. Known quenching mechanisms encompass enzymes such as superoxide dismutase and catalase or non-enzymatic antioxidants like glutathione, carotenoids and α-tocopherol (vitamin E) 18 . In plants, ROS and in particular 1 O 2 production has been shown to occur at photosystem II upon illumination with visible light 19,20 . In cyanobacteria, shorter wavelengths such as ultraviolet radiation (UVR, <400 nm), are known to induce ROS, causing DNA damage, lipid-peroxidation and overall decreased photosynthetic efficiency 21,22 . To our knowledge no study has investigated the effect of NIR on ROS production in cyanobacteria.
Relative levels of ROS can be estimated through measurements of e.g. gene expression 23 , ROS sensitive fluorescence probes 24 and enzyme activity 25 . These methods provide integrated values of ROS production over incubation time intervals ranging from minutes to hours. In this study we used a fast and sensitive laser photo-acoustic gas detector 26 that can measure the ethylene produced from the reaction of certain types of ROS with the substrate 2-keto-4-thiomethylbutyric acid (KMBA), previously added to the samples. Such near real-time ROS detection is valuable in determining the immediate effect of treatments on the physiological state and stress level within living organisms. KMBA is thought to diffuse into intact cells 27 and, when supplied at saturating concentrations outcompetes other radical scavenging mechanisms. In the KMBA assay, the butyric acid moiety is known to react with the ROS peroxynitrite, hydroxyl radicals and peroxyl radicals 28 , resulting in the formation of ethylene, which can then be quantified. Whether singlet oxygen and superoxide anions react with KMBA and subsequently form ethylene has not been investigated yet. In other studies, KMBA has been used to test the antioxidant capacity of radical scavengers via their ability to inhibit ethylene formation relative to a control reaction (total oxyradical scavenging capacity, TOSC) 28,29 .
In this study, we report the effect of light intensity and spectral composition on ROS generation, as measured in real-time using a laser-photoacoustic gas detector in three different strains of NIR utilizing cyanobacteria belonging to the genus Acaryochloris, including a new strain (named Acaryochloris CRS), isolated from phototrophic biofilms growing on dead coral branches collected on Heron Island, Australia.

Results and discussion
We aimed to determine the stress levels associated with Chl d-driven oxygenic photosynthesis and tested NIR, VIS and more narrow wavebands for their capacity to induce ROS in three strains of Acaryochloris: i) The Acaryochloris marina type strain MBIC11017 2,3 , ii) strain HICR111A 5 and, iii) a novel strain, named CRS, isolated from dead coral branches which, based on 16S rRNA gene sequencing, grouped within the genus Acaryochloris ( Figure 1). Acaryochloris strains MBIC11017 and HICR111A are both well described in terms of their photopigmentation, genomic content, ultrastructure and their capability to perform photoacclimation 4,5,30 . To test whether photoacclimation, i.e., light-dependent change in pigment levels, was associated with increased resistance or sensitivity towards ROS, we acclimated the strains to NIR or VIS prior to experiments.
(ii) Exposure to shorter wavelengths such as blue and cyan, generated the most ROS in strain MBIC11017 and HICR111A, while less ROS was produced upon exposure to longer wavelengths (green, amber and red) ( Figure 2C).
(iii) Strain CRS generated less ROS upon exposure to VIS when previously acclimated to NIR, while strain MBIC11017 and HICR111A appear more sensitive to VIS when adapted to NIR ( Figure 2A).
In Acaryochloris, VIS irradiance is primarily absorbed by the photopigments Chl d (with maximum absorption occurring at 440-470/710 nm), Chl a (440-470/675 nm), carotenoids (440-520 nm) and if present, phycobiliproteins (560-650 nm). NIR provides a more targeted stimulation of photosynthesis and is almost exclusively absorbed by Chl d. At comparable photon irradiances (VIS = 340-480 µmol m -2 s -1 versus NIR = 400 µmol m -2 s -1 ), we found that, depending on strain and previous adaptation, ROS levels were lower in cells exposed to NIR than in those exposed to VIS ( Figure 2A). Based on pulse-amplitude modulated (PAM) fluorometry measurements the light intensities used in our experiments are known to saturate relative-electron transport rates in the type strain MBIC11017 12 . Photoinhibition is not observed even at higher, photon irradiance, but we hypothesize that prolonged exposure to relatively high-irradiances (10-20 fold more irradiance than during culturing for 15-20 min) could result in the over-reduction of the primary acceptors on the PSI and PSII side resulting in the production of ROS 15,23 . This over-reduction could lead to the transfer of electrons to O 2 , the subsequent generation of superoxide radical, followed by their conversion to hydrogen peroxide as well as hydroxyl radicals 23,31 . Alternatively, ROS generation could occur via photosensitized light-harvesting pigments 32 ; however, in intact light-harvesting complexes the efficiency of electron transfer towards the reaction centers is usually outcompeting the formation of long-lived (ROS-forming) chlorophyll triplet states 33 . This appears particularly true for the unique phycobiliprotein antenna rods in A. marina MBIC11017, in which excitation electron transfers to PSII were found to be significantly faster than in Chl a-containing cyanobacteria 34 . Additionally, it is known that within light-harvesting complexes carotenoids are outcompeting O 2 in the de-excitation of triplet chlorophyll states 35 . All three strains used in the current study were found to contain zeaxanthin (Table 1) as well as α-carotene, these carotenoids will bring about rapid quenching of excited Chl states and if necessary can also quench singlet oxygen and aid in general non-photochemical quenching 33,36 .
Exposure to shorter wavelengths, such as blue (470 nm) and cyan (495 nm) light generated the most ROS in strain MBIC11017 and HICR111A, while less ROS was produced upon exposure to longer wavelengths (green, amber and red) ( Figure 2C). Blue and cyan light-induced ROS production in MBIC11017 and HICR111A is probably due to spectral overlap with the Soret-band absorption of By taking advantage of the real-time ROS detection method, we could for the first time demonstrate the immediate effects of NIR, VIS and other wavelengths on the generation of certain ROS within living cyanobacteria. Specifically, we found that: (i) Depending on strain and previous adaptation, ROS levels were lower in cells exposed to NIR than in those exposed to VIS ( Chl a/d (440-470 nm) ( Figure 2B) and the above-mentioned mechanisms in ROS generation. Red (645 nm), amber (595 nm) and green (535 nm) light overlaps with the absorption spectra of phycobiliproteins which, if present, aid in light harvesting and excitation energy transfer towards the photosystems 34 . Strain MBIC11017 is known to express the phycobiliproteins phycocyanin and allophycocyanin 37 , while strain HICR111A reportedly lacks phycobiliproteins 5 .
Comparable ROS levels were observed in strain HICR111A and MBIC11017 under yellow and green light, suggesting the presence of pigments absorbing these wavelengths or the possibility of other light-induced ROS production mechanisms. Spectrophotometric analysis of the strains showed weak absorption in the phycobiliprotein-specific region within all three strains ( Figure 3). This would corroborate the excitation energy transfer to PSI and II in strain HICR111A and could explain the observed ROS production under yellow and green light. However this would also refute previous reports on the absence of phycobiliproteins in this strain 5 . Given that phycobiliproteins were not purposely extracted, and further analyzed, in the present study, we can at this point only speculate about their presence and relative expression under different growth conditions.
There is a long history of associating pigment compositions within phototrophs with the spectral composition of ambient light and exposure history: for recent work see 38 and 23 , respectively. These two factors are likely to determine the sensitivity of phototrophs to irradiance and their capability to cope with ROS levels generated upon irradiation. Interestingly, we found that strain CRS generated very little ROS upon exposure to VIS when previously acclimated to NIR, while strain MBIC11017 and HICR111A appear to be more sensitive to VIS when previously adapted to NIR (Figure 2A). HPLC analysis revealed a higher ratio of zeaxanthin/α-carotene in NIR-acclimated CRS cells than in the other two strains (Table 1), albeit with a relatively large standard error. In A. marina MBIC11017 α-carotene was found to be an integral part of both photosystem reaction center cores 39,40 and zeaxanthin is predominantly found in the periphery of light-harvesting complexes 36 .
Based on the higher zeaxanthin/α-carotene ratios in NIR-adapted cells of all three strains we hypothesize that there are slightly more antenna complexes (zeaxanthin and Chl d) in NIR-adapted cells than in those pre-adapted to VIS, thus providing more potential for ROS production/quenching. Given that the antenna complexes are predominantly composed of Chl d and thus absorb in the NIR part of the light spectrum, this chromatic photoacclimation is expected and further corroborated by higher Chl d/zeaxanthin ratios in NIR-adapted strains in this study. We hypothesize that the higher contribution of zeaxanthin in the NIR-adapted strain CRS could aid in effectively capturing NIR but potentially also in quenching ROS produced during illumination with either VIS or NIR. However, we acknowledge that this hypothesis is based on HPLC analysis of pigment levels with a relatively high variability and one individual ROS measurement.
Besides their light harvesting capability carotenoids (including zeaxanthin) are also known for their antioxidative abilities 15,35 . It is known that zeaxanthin mostly operates outside of the reaction centers (RC) and is predominantly found within the peripheral light-harvesting complexes 35 . Here, zeaxanthin was shown to play a crucial role in non-photochemical quenching and energy dissipation from sensitized chlorophyll molecules or singlet oxygen 35 . Singlet-oxygen formation is often inevitable and is believed to necessitate the rapid turnover of the photosystem II-D1 polypeptide 41 . It was found that the PSII-D2 protein acquires a certain photoprotection against singlet-oxygen by close association with β-carotene molecules in the RC of PSII 42,43 and hence has a lower turnover than the D1 protein. Lastly, it is possible that strain specific differences in ROS production are associated with dissimilarities in growth forms: Strain HICR111A forms cell aggregates 5 , and so does strain CRS ( Figure 2B), whereas strain MBIC11017 usually grows as dispersed cells 5 but can be immobilized into biofilms 45 . The formation of aggregates in strain HICR111A and CRS might provide photoprotection through self-shading, a behavior reportedly less pronounced in strain MBIC11017 5 . Both HICR111A and CRS originate from shallow reef flats, a high irradiance habitat. In contrast, strain MBIC11017 was isolated from a didemnid ascidian 2 , a light environment depleted of VIS but with sufficient NIR 10-12 .
Based on these first, preliminary, measurements, we suggest that through utilization of NIR, Acaryochloris can avoid a considerable amount of light stress, while harvesting a portion of the electromagnetic radiation spectrum not used by other oxyphototrophs. Additionally, aggregation of certain strains could protect against excess amounts of ROS generated during high irradiance exposure. Overall, this could add further arguments as to why Acaryochloris is a successful and apparently globally widespread oxy phototroph 11 .

Materials and methods
Isolation of the novel Acaryochloris strain CRS Dead coral branches with patches of faint yellow-greenish pigmentation were collected during low tide from coral patches on the inner reef flat off Heron Island, Queensland, Australia (see more details on the sampling site in 10 . The samples were transported back to the lab in a container with seawater and immediately placed into outdoor aquaria that were continuously flushed with aerated ambient seawater pumped in from the reef flat. Bacterial cells found on the dead coral branch were removed using a sterile scalpel and immediately placed into KESM media and kept under dim visible light for three days. After transportation to Sydney the cells were kept in KESM media under NIR LEDs (centered at 720 nm, Cat. No. L720-04AU, Epitex Inc., Japan). NIR irradiance was set to ~5 µmol photons m -2 s -1 using a SKP200 light meter equipped with a SKP216ER irradiance sensor with a 550 to 750 nm light sensitivity range (Skye Instruments, United Kingdom). After three weeks, the growing cells were diluted into aliquots of fresh KESM medium. After additional incubation, the pigmentation of the cells was inspected by measuring their absorption characteristics using a spectrophotometer (UV-2550, Shimadzu, Japan). The cells were hereafter maintained in KESM media under NIR.
Acaryochloris growth conditions Acaryochloris strains MBIC110771, HICR111A and the newly isolated Acaryochloris strain CRS were grown in 200 ml cell culture flasks in marine KESM media (salinity of 30) in a shaking incubator at 28°C as previously reported 1 . All cultures were shaken at 100 rpm under a 12/12 h light-dark shift. Near infrared radiation (NIR) was provided by narrow band LEDs (L720-04AU, 700-740 nm, centered at 720 nm, Epitex Inc., Japan) at an irradiance of 20-40 µmol photons m -2 s -1 . Another set of cultures was grown under the same irradiance but using visible light delivered by a halogen lamp equipped with a heat filter (HQ Power, Brinck Elektronik, Denmark). Absolute irradiance measurements of NIR and visible light were done with a calibrated spectroradiometer (Jaz ULM-200, Ocean Optics, Dunedin, FL, USA).

DNA extraction and PCR amplification
Six ml of dense cell culture was spun down and then extracted using the FastDNA for Soil kit (MP Biomedicals, France) using the manufacturers standard protocol. The resulting DNA was quantified using the Qubit system (Invitrogen, Life Technologies Europe, USA) and diluted 1:10 using molecular grade water. The 16S rRNA gene was amplified using the primers 16SCYfw (5′-GGCTCAGGATGAACGCTGGCGG-3′) and 16SCYrv (5′-ACCTTGTTACGACTTCACCCCAGTC-3′) using the PCR Master (Roche, Switzerland) with 30 amplification cycles. The resulting PCR product was purified on an agarose gel and the band excised using a sterile scalpel. DNA was extracted from the excised gel using the QiaexII gel extraction kit (Qiagen Nordic, Sweden) and then cloned into the pCR4-TOPO cloning vector (Invitrogen, Life Technologies Europe, USA) and transformed into One-Shot TOP-10 chemically competent cells (Invitrogen, Life Technologies Europe, USA). Clones were subsequently grown in LB-medium, plasmids were extracted using the Qiaprep kit (Qiagen Nordic, Sweden), and checked for correct

ROS measurements via real-time ethylene detection
Real-time ethylene production was measured using a laser-based photo-acoustic ethylene detector (ETD-300, Sensor Sense, the Netherlands) combined with an in-line gas-flow through system (Valve Controller VC 6, Sensor Sense, the Netherlands). The system was described in reference 26 . Custom made gas-tight incubation chambers were connected via the valve controller to the ETD, which could sequentially sample ethylene fluxes from the different incubators. The incubator was made of anodized aluminum (51ST quality) and contained a cooling/heating channel to control temperature and a glass window to supply light to the samples (see details in 48 ). The incubator could hold 2 ml aliquots of Acaryochloris culture. To ensure steady state ethylene fluxes at the moment a sample was connected to the ETD, we supplied a continuous flow of moisturized air (2 l h -1 ) over every individual incubator during the experiments. The air was moisturized by flushing it through gas tight vials filled with de-ionized water; this was necessary to prevent evaporation of media in the incubator. The system was continuously controlled for gas leaks, by automated comparison of the incoming and outgoing gas flow. The outlet of the incubator was connected to a CO 2 trap (KOH pellets) and water scrubber (CaCl 2 ) placed before the ethylene detector. The valve controller allowed each measuring chamber to be alternately connected for 20 minutes to the ethylene detector. Steady state ETD readings from the cultures were obtained within ~4 minutes after connection to the ETD. The ETD-300 has a sample frequency of ~12 samples min -1 and the concentrations of the last two minutes per treatment were averaged. Typical standard deviations were 0.15 ppbv for ethylene measurements under steady state conditions. The averaged concentrations were normalized to the amount of Chl d present in the cultures to correct for differences in biomass between samples.

Light experiments
Light dependent ROS production was measured using both visible light (400-700 nm) and near-infrared radiation (NIR). For visible wavelengths, we used an incubator setup (Mini-Incubator, Sensor Sense, Nijmegen, The Netherlands), fitted with an array of 11 1W cool white LEDs (Luxeon Star, 1W, Lumileds, USA) connected to a PC-driven controller. Irradiance levels were set between 340-480 µmol photons m -2 s -1 for visible light. Different irradiance levels were adjusted by varying the electrical current of the LED array via a special software routine (Sensor Sense, Nijmegen, The Netherlands) and measuring the downwelling irradiance with a calibrated light meter (LI250, LiCOR Biosciences, Lincoln, USA).
For NIR exposure, the actinic light was provided by four collimated NIR LEDs (M3L1-720-30, 700-740 nm, centered at 720 nm, sized inserts using gel electrophoresis. Three clones were sent off for subsequent sequencing by a commercial provider (Macrogen, Seoul, Korea).

Phylogenetic analysis
Cyanobacterial 16S rRNA gene sequences were retrieved from the SILVA database (http://www.arb-silva.de/) and aligned together with sequences retrieved from clones using MUSCLE as implemented in the Molecular Genetic Analysis (MEGA) software package version 5.0. Neighbor-joining (NJ) was used to infer phylogenetic relationships among sequences; support values with Jukes-Cantor distances and 10000 bootstrap replicates are displayed next to branches displayed in the phylogenetic tree ( Figure 1).

Chlorophyll extraction and spectrophometry
Two ml of each culture were pelleted by centrifugation at 8000 × g. The supernatant was removed, while the resulting pellet was re-suspended in 96% ethanol and incubated at 4°C for 60 min in darkness. During the ethanol extraction, the samples were vortexed at maximal speed every 15 minutes. After one hour, the cells were pelleted by centrifugation at 8000 x g and the supernatant was used to determine Chl d concentrations via spectrophotometry (UV-2101PC, Shimadzu, Japan) according to Ritchie 46 . The same spectrophotometer was used to measure the in vivo absorbance spectra of the different cultures. Acaryochloris strains HICR111A and CRS proved very difficult to keep in suspension and were therefore sonicated (Misonix sonicator 4000, Qsonica LLC., Newtown, CT, USA) for one minute at maximum speed prior to spectrophotometric measurements. To prevent bleaching of the photopigments, all handling was done as quickly as possible and under low-light conditions.

HPLC-based pigment analysis
For HPLC analysis, 2 ml of Acaryochloris cultures were spun down at maximum speed (~13,000 rpm) in a bench centrifuge, the supernatant was removed and the remaining pellet resuspended in cold acetone-methanol (7:2 by vol) and the cells sonicated for 20s using a Misonix sonicator 4000 (Qsonica LLC., Newtown, CT, USA) according to 47

Competing interests
There are no competing interests.

Grant information
The work was supported by the Danish Council for Independent Research | Natural Sciences (FNU), project 11-108257, and the EU-FP6-Infrastructures-5 program, project FP6-026183 'Life Science Trace Gas Facility'.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
oxygen species (ROS) are formed. The authors conclude that this is a strategy of this genus (more species of which are being discovered widely around the planet) to protect against photodamage during high irradiance exposure -a more and more likely occurrence these days.
The authors stress the point (page 7, left, para 3) that this is a preliminary study in which fully replicated measurements of ROS were not possible. I understand this constraint and accept that reporting measurements of ROS, using the novel technique of real time ethylene detection, from is Acaryochloris very interesting but I feel the paper goes too far in its claims. It also is unclear about the different types of ROS detected and the mechanism by which protection is provided by carotenoids.3, right para 2.
The ROS detection method (real time ethylene detection RTED) described in ref 28 (Regoli and Winston) appears to only directly detect very strong oxidants hydroxyl and peroxyl radicals and peroxynitrite. It does not directly detect superoxide or singlet oxygen (1O2). This should be made clearer in the text and there should be discussion about production of hydroxyl radicals. Relating to point 1.: The correlation between light-induced increase in relative amounts of the zeaxanthin containing antenna complexes and the ROS levels detected by the RTED system should be explained in more detail. Carotenoids in photosynthetic complexes mainly operate by quenching chlorophyll triplet states before they can form 1O2 or they directly quench any 1O2 that is formed. They do also quench oxygen radicals but these are more likely to be produced in the aqueous phase (e.g. from reduced ferredoxin in PSI) where they are usually quenched by antioxidant enzymes such as ascorbate peroxidase etc. Though it is possible alpha-Car in the PSII reaction center could quench radicals produced from reduced quinone. When the ROS levels, detected by RTED, increase it is likely that other ROS (e.g. superoxide) and perhaps 1O2 also increase and so carotenoids would be helpful. However, the text makes it sound as if in CRS the zeaxanthin level increases relative to chlorophyll when it is simply more antenna (Zea plus Chl ) d being produced and so there is more potential for 1O2 production. Essentially I feel the text, though cautious, claims too much. The errors on the pigment levels especially for CRS (they are huge) suggest the very different values for NIR and VIS adapted cells could be a fluke. Also the single point for CRS in Fig. 2A NIR adapted under VIS exposure could be a fluke. Minor Points p. 4 end para beginning 'In ....: Change last sentence round so it says: zeaxanthin will bring Acaryochloris about rapid quenching of excited chlorophyll states and if necessary can also quench singlet oxygen -or something similar to this. p.6 end para 3: Rephrase: ...and zeaxanthin is restricted to the peripheral light-harvesting complexes (PCB proteins). p.6 Second sentence from bottom: I do not like the sentence emphasising that zeaxanthin quenches singlet oxygen. The a-carotene in the reaction centre is at least as likely to be quenching singlet oxygen as it is well known it cannot directly quench the radical pair triplet state as it is bound to far away from the highly oxidising primary electron donor. The reference to energy dissipation by zeaxanthin is irrelevant here. I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.
No competing interests were disclosed. Competing Interests: appears to have been conducted following appropriate scientific standards and protocols, and using valid methods.
:3rd from last paragraph: "concretionary" is not a common term to define coral Results and Discussion reef substrata I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.
No competing interests were disclosed. Competing Interests: