REVIEW—ULTRAVIOLET RADIATION‐ABSORBING MYCOSPORINE‐LIKE AMINO ACIDS IN CORAL REEF ORGANISMS: A BIOCHEMICAL AND ENVIRONMENTAL PERSPECTIVE

Coral bleaching: causes and consequences

Brown, B. (1997) · Coral reefs · doi:10.1007/s003380050249 · Cited by 1,657

Reef Corals: Mutualistic Symbioses Adapted to Nutrient-Poor Environments

MUSCATINE, L., & Porter, J. W. (1977) · BioScience · doi:10.2307/1297526 · Cited by 1,249

Coral reef bleaching: facts, hypotheses and implications

Glynn, P. (1996) · Global Change Biology · doi:10.1111/j.1365-2486.1996.tb00063.x · Cited by 980

Landscape ecology of algal symbionts creates variation in episodes of coral bleaching

Rowan, R., Knowlton­, N., Baker, A. C., & Jara, J. (1997) · Nature · doi:10.1038/40843 · Cited by 783

The Shikimate Pathway — A Metabolic Tree with Many Branche

Bentley, R., & Haslam, E. (1990) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409239009090615 · Cited by 732

The role of symbiotic algae in carbon and energy flux in reef corals

MUSCATINE, L. (1990) · Paardenkrant horses.nl/Ecosystems of the world · Cited by 655

[3] Free radical initiators as source of water- or lipid-soluble peroxyl radicals

Niki, E. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86095-d · Cited by 574

Intraspecific diversity and ecological zonation in coral-algal symbiosis.

Rowan, R., & Knowlton­, N. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2850 · Cited by 567

Microenvironment and photosynthesis of zooxanthellae in scleractinian corals studied with microsensors for O2, pH and light

Kühl, M., Cohen, Y., Dalsgaard, T., Jørgensen, B. B., & Revsbech, N. P. (1995) · Marine Ecology Progress Series · doi:10.3354/meps117159 · Cited by 561

Temperature Stress Causes Host Cell Detachment in Symbiotic Cnidarians: Implications for Coral Bleaching

Gates, R. D., Baghdasarian, G., & MUSCATINE, L. (1992) · Biological Bulletin · doi:10.2307/1542252 · Cited by 526

Variation in sunscreen compounds (mycosporine‐like amino acids) for marine species along a gradient of ultraviolet radiation transmission within doubtful sound, New Zealand

Lamare, M. D., Lesser, M. P., Barker, M., Barry, T. M., & Schimanski, K. B. (2004) · New Zealand Journal of Marine and Freshwater Research · doi:10.1080/00288330.2004.9517277 · Cited by 30

UV-absorbing bacteria in coral mucus and their response to simulated temperature elevations

Ravindran, J., Kannapiran, E., Manikandan, B., Francis, K., Arora, S., Karunya, E., Kumar, A., Singh, S., & Jose, J. (2013) · Coral Reefs · doi:10.1007/s00338-013-1053-x · Cited by 29

Aeroterrestrial Algae Growing on Man-Made Surfaces

Karsten, U., Schumann, R., & Mostaert, A. S. (2007) · Cellular origin and life in extreme habitats · doi:10.1007/978-1-4020-6112-7_32 · Cited by 31

Ultraviolet-Light-Absorbing Tunic Cells in Didemnid Ascidians Hosting a Symbiotic Photo-oxygenic Prokaryote,Prochloron

Maruyama, T., Hirose, E., & Ishikura, M. (2003) · Biological Bulletin · doi:10.2307/1543546 · Cited by 28

Mycosporine-Like Amino Acids (MAAs) Profile of Two Marine Red Macroalgae, Gelidium sp. and Ceramium sp.

Pandey, A., Pandey, S., Rajneesh, Pathak, J., Ahmed, H., Singh, V., Singh, S. P., & Sinha, R. P. (2017) · International Journal of Applied Sciences and Biotechnology · doi:10.3126/ijasbt.v5i1.16568 · Cited by 29

Fish mucus versus parasitic gnathiid isopods as sources of energy and sunscreens for a cleaner fish

Eckes, M., Dove, S., Siebeck, U. E., & Grutter, A. S. (2015) · Coral Reefs · doi:10.1007/s00338-015-1313-z · Cited by 28

Characterization of the diversity of mycosporine-like amino acids in lichens from high altitude region of Himalaya

Shukla, V., Kumari, R., Patel, D. K., & Upreti, D. K. (2015) · Amino Acids · doi:10.1007/s00726-015-2069-z · Cited by 27

Surviving but not thriving: inconsistent responses of zooxanthellate jellyfish polyps to ocean warming and future UV-B scenarios

Klein, S. G., Pitt, K. A., & Carroll, A. R. (2016) · Scientific Reports · doi:10.1038/srep28859 · Cited by 25

Australasian research on marine natural products: chemistry, bioactivity and ecology

Volkman, J. K. (1999) · Marine and Freshwater Research · doi:10.1071/mf99084 · Cited by 27

Peroxide scavenging potential of ultraviolet-B-absorbing mycosporine-like amino acids isolated from a marine red alga Bryocladia sp.

Kannaujiya, V. K., RICHA, R., & Sinha, R. P. (2014) · Frontiers in Environmental Science · doi:10.3389/fenvs.2014.00026 · Cited by 26

Mycosporine-like amino acid content in the sea anemones Aulactinia marplatensis, Oulactis muscosa and Anthothoe chilensis

Arbeloa, E. M., Carignan, M. O., Acuña, F. H., Churio, M. S., & Carreto, J. I. (2010) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2010.03.011 · Cited by 26

Sensitivity of freshwater macrophytes to UV radiation: relationship to depth zonation in an oligotrophic New Zealand lake

Rae, R., Rae, R., Hanelt, D., Hanelt, D., Hawes, I., & Hawes, I. (2001) · Marine and Freshwater Research · doi:10.1071/mf01016 · Cited by 26

Robust natural ultraviolet filters from marine ecosystems for the formulation of environmental friendlier bio-sunscreens

Amador-Castro, F., Rodríguez‐Martínez, V., & Carrillo-Nieves, D. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.141576 · Cited by 28

Comparative sensitivity of the early life stages of a coral to heavy fuel oil and UV radiation

Nordborg, F. M., Brinkman, D. L., Ricardo, G. F., Agustı́, S., & Negri, A. P. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.146676 · Cited by 25

Polyols and UV ‐sunscreens in the Prasiola‐clade (Trebouxiophyceae, Chlorophyta) as metabolites for stress response and chemotaxonomy

Hotter, V., Glaser, K., Hartmann, A., Ganzera, M., & Karsten, U. (2018) · Journal of Phycology · doi:10.1111/jpy.12619 · Cited by 24

The role of host-based color and fluorescent pigments in photoprotection and in reducing bleaching stress in corals

Salih, A., Cox, G. C., Szymczak, R., Coles, S. L., Baird, A. H., Dunstan, A., Cocco, G., Mills, J., & Larkum, A. W. D. (2006) · ResearchOnline at James Cook University (James Cook University) · Cited by 23

Monitoring defensive responses in macroalgae – limitations and perspectives

Barre, S., Weinberger, F., Kervarec, N., & Potin, P. (2004) · Phytochemistry Reviews · doi:10.1007/s11101-005-1459-3 · Cited by 24

Effects of reduced UV radiation on a microbenthic community during a microcosm experiment

le Roux, R., Gosselin, M., Desrosiers, G., & Nozais, C. (2002) · Marine Ecology Progress Series · doi:10.3354/meps225029 · Cited by 24

Ontogeny of tolerance to and avoidance of ultraviolet radiation in red sea bream Pagrus major and black sea bream Acanthopagrus schlegeli

Fukunishi, Y., Masuda, R., & Yamashita, Y. (2006) · Fisheries Science · doi:10.1111/j.1444-2906.2006.01157.x · Cited by 23

Response to short term ultraviolet stress in the reef-building coral Pocillopora capitata (Anthozoa: Scleractinia)

Liñán‐Cabello, M. A., Flores‐Ramírez, L. A., Cobo-Díaz, J. F., Zenteno‐Savín, T., Olguín-Monroy, N. O., Ortiz, A. O., & Gomez, A. T. (2009) · Revista de Biología Tropical · doi:10.15517/rbt.v58i1.5197 · Cited by 23

Ultraviolet-absorbing compounds in the mucus of shallow-dwelling tropical reef fishes correlate with environmental water clarity

Zamzow, J. P. (2007) · Marine Ecology Progress Series · doi:10.3354/meps06890 · Cited by 23

Microalgae: A Renewable Source of Bioproducts

Blackburn, S. I., & Volkman, J. K. (2012) · Wiley eBooks · doi:10.1002/9781119946083.ch9 · Cited by 24

The biology of an Antarctic rhodophyte,Palmaria decipiens: recent advances

Becker, S., Quartino, M. L., Campana, G. L., Bucolo, P., Wiencke, C., & Bischof, K. (2011) · Antarctic Science · doi:10.1017/s0954102011000575 · Cited by 21

Effects of Global Change, Including UV and UV Screening Compounds

RICHA, R., Sinha, R. P., & Häder, D. (2016) · Springer eBooks · doi:10.1007/978-3-319-24945-2_17 · Cited by 22

Photobiological Aspects of the Mutualistic Association Between Paramecium bursaria and Chlorella

Sommaruga, R., & Sonntag, B. (2009) · Microbiology monographs · doi:10.1007/978-3-540-92677-1_5 · Cited by 22

Effects of ultraviolet radiation and water motion on the reef coral, Porites compressa Dana: a transplantation experiment

Kuffner, I. (2002) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/s0022-0981(02)00031-x · Cited by 22

Corals: Environmental Controls on Growth

(2012) · Springer eBooks · doi:10.1007/springerreference_205797 · Cited by 21

Kocuria Strains from Unique Radon Spring Water from Jachymov Spa

Timkina, E., Drábová, L., Palyzová, A., Řezanka, T., Maťátková, O., & Kolouchová, I. (2022) · Fermentation · doi:10.3390/fermentation8010035 · Cited by 23

Interactive effects of solar radiation and inorganic nutrients on biofiltration, biomass production, photosynthetic activity and the accumulation of bioactive compounds in Gracilaria cornea (Rhodophyta)

Figueroa, F. L., Álvarez‐Gómez, F., Bonomi‐Barufi, J., Vega, J., Massocato, T. F., Gómez‐Pinchetti, J. L., & Korbee, N. (2022) · Algal Research · doi:10.1016/j.algal.2022.102890 · Cited by 20

Negative response of photosynthesis to natural and projected high seawater temperatures estimated by pulse amplitude modulation fluorometry in a temperate coral

Caroselli, E., Falini, G., Goffredo, S., Dubinsky, Z., & Levy, O. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00317 · Cited by 20

Chapter 17 Vulnerability of coral reefs of the Great Barrier Reef to climate change

Fabricius, K., Hoegh‐Guldberg, O., Johnson, J. E., McCook, L. J., & Lough, J. (2007) · GBRMPA ELibrary (Great Barrier Reef Marine Park Authority) · Cited by 19

Enhanced ultraviolet radiation can terminate sexual reproduction in the broadcasting coral species Acropora cervicornis Lamarck

Torres, J. L., Armstrong, R. A., & Weil, E. F. (2008) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2008.01.022 · Cited by 19

PSII activity and pigment dynamics of Symbiodinium in two Indo-Pacific corals exposed to short-term high-light stress

Krämer, W. E., Schrameyer, V., Hill, R., Ralph, P. J., & Bischof, K. (2012) · Marine Biology · doi:10.1007/s00227-012-2113-4 · Cited by 16

Temporal changes in environmental conditions of a mid-latitude estuary (southern Chile) and its influences in the cellular response of the euryhaline anemone Anthopleura hermaphroditica

Cubillos, V. M., Ramírez-Kuschel, E., Cruces, E., Montory, J. A., Segura, C. J., & Mardones, D. (2018) · Ecological Indicators · doi:10.1016/j.ecolind.2018.01.015 · Cited by 17

Response of fluorescence morphs of the mesophotic coral Euphyllia paradivisa to ultra-violet radiation

Ben‐Zvi, O., Eyal, G., & Loya, Y. (2019) · Scientific Reports · doi:10.1038/s41598-019-41710-3 · Cited by 16

Ontogenetic change in the abundance of mycosporine-like amino acids in non-zooxanthellate coral larvae

YAKOVLEVA, I. M., & Baird, A. H. (2005) · Coral Reefs · doi:10.1007/s00338-005-0005-5 · Cited by 17

Adaptation to UV Stress in Algae

Häder, D. (2001) · Springer eBooks · doi:10.1007/978-3-642-59491-5_7 · Cited by 17

The interactive impacts of a constant reef stressor, ultraviolet radiation, with environmental stressors on coral physiology

Downie, A. T., Cramp, R. L., & Franklin, C. E. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.168066 · Cited by 16

Comparison of physiological and transcriptome responses of corals to strong light and high temperature

Jia, S., Geng, X., Cai, Z., Wang, Y., Shen, J., Li, Y., Wu, Z., Chen, S., & Wang, D. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116143 · Cited by 16

Sex and microhabitat influence the uptake and allocation of mycosporine-like amino acids to tissues in the purple sea urchin, Strongylocentrotus purpuratus

Gravem, S. A., & Adams, N. L. (2012) · Marine Biology · doi:10.1007/s00227-012-2045-z · Cited by 15

Coral Bleaching

Plass-Johnson, J. G., Cardini, U., van Hoytema, N., Bayraktarov, E., Burghardt, I., Naumann, M. S., & Wild, C. (2014) · Springer eBooks · doi:10.1007/978-94-017-9499-2_9 · Cited by 16

Mycosporine-like amino acid (MAAs) production by Heterocapasa sp. (Dinophyceae) in indoor cultures

Montero, O. (2003) · Biomolecular Engineering · doi:10.1016/s1389-0344(03)00050-9 · Cited by 15

Biomedical Applications of Mycosporine‐Like Amino Acids

RICHA, R., & Sinha, R. P. (2013) · Wiley eBooks · doi:10.1002/9783527665259.ch27 · Cited by 15

A Pollen Diet Confers Ultraviolet-B Resistance in Phytoseiid Mites by Providing Antioxidants

Sugioka, N., Kawakami, M., Hirai, N., & Osakabe, M. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00133 · Cited by 11

The Effects of Supply on Mazzaella laminarioides (Rhodophyta, Gigartinales) from Southern Chile

Navarro, N. P., Figueroa, F. L., Korbee, N., Mansilla, A., Matsuhiro, B., Barahona, T., & Plastino, E. M. (2014) · Photochemistry and Photobiology · doi:10.1111/php.12344 · Cited by 14

The Effects of UV Radiation on Chloroplast Clumping and Photosynthesis in the SeagrassHalophila stipulaceaGrown under High-PAR Conditions

Sharon, Y., Dishon, G., & Beer, S. (2011) · Journal of Marine Biology · doi:10.1155/2011/483428 · Cited by 14

Lebensraum Fassade: Aeroterrestrische Mikroalgen

Karsten, U., Schumann, R., Häubner, N., & Friedl, T. (2005) · Biologie in unserer Zeit · doi:10.1002/biuz.200410269 · Cited by 14

The occurrence of mycosporine-like amino acids in the gametophytic and sporophytic stages ofBangia(Bangiales, Rhodophyta)

Boedeker, C., & Karsten, U. (2005) · Phycologia · doi:10.2216/0031-8884(2005)44[403:toomaa]2.0.co;2 · Cited by 14

Response of the soft coral Heteroxenia fuscescens to ultraviolet radiation regimes as reflected by mycosporine-like amino acid biosynthesis

Ben-Yosef, D., Kashman, Y., & Benayahu, Y. (2006) · Marine Ecology · doi:10.1111/j.1439-0485.2006.00111.x · Cited by 13

Mycosporine-like amino acids vs carrageenan yield inMazzaella laminarioides(Gigartinales; Rhodophyta) under high and low UV solar irradiance

Navarro, N. P., Figueroa, F. L., & Korbee, N. (2017) · Phycologia · doi:10.2216/16-124.1 · Cited by 14

Bio‐Inspired Molecules Extracted from Marine Macroalgae: A New Generation of Active Ingredients for Cosmetics and Human Health

Stiger‐Pouvreau, V., & Guérard, F. (2018) · Blue Biotechnology · doi:10.1002/9783527801718.ch22 · Cited by 14

Ultraviolet-B Wavelengths Regulate Changes in UV Absorption of Cleaner Fish Labroides dimidiatus Mucus

Zamzow, J. P., Siebeck, U. E., Eckes, M., & Grutter, A. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078527 · Cited by 14

Effects of Salinity and Ultraviolet Radiation on the Bioaccumulation of Mycosporine‐like Amino Acids in Artemia from Lake Urmia (Iran)

Khosravi, S., Khodabandeh, S., Agh, N., & Bakhtiarian, M. (2012) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2012.01245.x · Cited by 13

Differential responses of tetrasporophytes and gametophytes of Mazzaella laminarioides (Gigartinales, Rhodophyta) under solar UV radiation

Navarro, N. P., Figueroa, F. L., Korbee, N., Mansilla, A., & Plastino, E. M. (2016) · Journal of Phycology · doi:10.1111/jpy.12407 · Cited by 13

Embryonic buoyancy control as a mechanism of ultraviolet radiation avoidance

Pasparakis, C., Wang, Y., Stieglitz, J. D., Benetti, D. D., & Grosell, M. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.10.093 · Cited by 13

Exposure of eggs to solar UV‐B leads to reduced hatching rates in two sparid fishes, red sea bream Pagrus major and black sea bream Acanthopagrus schlegeli

Fukunishi, Y., Masuda, R., & Yamashita, Y. (2010) · Journal of Fish Biology · doi:10.1111/j.1095-8649.2009.02517.x · Cited by 13

Coral health and disease in the Pacific : vision for action

Galloway, S. B., Woodley, C. M., & Bruckner, A. W. (2009) · AquaDocs (United Nations Educational, Scientific and Cultural Organization) · Cited by 13

Dermocosmetic applications of microalgal pigments

Baby, A. R., & Morocho‐Jácome, A. L. (2021) · Advances in applied microbiology · doi:10.1016/bs.aambs.2021.09.002 · Cited by 12

Electron partitioning in soluble organic products by wild-type and modified Synechocystis sp. PCC 6803

Nguyen, B. T., & Rittmann, B. E. (2016) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2016.04.016 · Cited by 12

Antioxidative and Antiglycative Properties of Mycosporine-Like Amino Acids-Containing Aqueous Extracts Derived from Edible Terrestrial Cyanobacteria

KORTEERAKUL, C., Honda, M., Ngoennet, S., Hibino, T., Waditee‐Sirisattha, R., & Kageyama, H. (2020) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.66.339 · Cited by 12

Biotechnological Potential of Macroalgae during Seasonal Blooms for Sustainable Production of UV-Absorbing Compounds

Rosic, N. N., & Thornber, C. (2023) · Marine Drugs · doi:10.3390/md21120633 · Cited by 13

Genome Mining as an Alternative Way for Screening the Marine Organisms for Their Potential to Produce UV-Absorbing Mycosporine-like Amino Acid

Rosic, N. N. (2022) · Marine Drugs · doi:10.3390/md20080478 · Cited by 11

Ecological and Physiological Responses of Macroalgae to Solar and UV Radiation

Gao, K., & Xu, J. (2010) · Cellular origin and life in extreme habitats · doi:10.1007/978-90-481-8569-6_11 · Cited by 11

Under high light stress two Indo-Pacific coral species display differential photodamage and photorepair dynamics

Schrameyer, V., Krämer, W. E., Hill, R., Jeans, J. A., Larkum, A. W. D., Bischof, K., Campbell, D. A., & Ralph, P. J. (2016) · Marine Biology · doi:10.1007/s00227-016-2940-9 · Cited by 11

Species-specific coral microbiome assemblages support host bleaching resistance during an extreme marine heatwave

Longley, R., Benucci, G. M. N., Pochon, X., Bonito, G. M., & Bonito, V. E. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.167803 · Cited by 10

Response of a rice-field cyanobacterium Anabaena sp. HKAR-7 upon exposure to ultraviolet-B radiation and ammonium chloride

Singh, D. K., Pathak, J., Pandey, A., Singh, V., Ahmed, H., Kumar, D., Rajneesh, & Sinha, R. P. (2020) · Environmental Sustainability · doi:10.1007/s42398-020-00146-6 · Cited by 10

UV Radiation Effects on Phytoplankton Primary Production: A Comparison Between Arctic and Antarctic Marine Ecosystems

Helbling, E., & Villafañe, V. (2002) · Ecological studies · doi:10.1007/978-3-642-56075-0_10 · Cited by 11

Sex-dependent effects of ultraviolet radiation on the marine amphipod Ampithoe valida (Ampithoidae)

Valiñas, M. S., & Helbling, E. W. (2015) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2015.02.025 · Cited by 10

Oxidative Challenges in Polar Seas

Regoli, F., Benedetti, M., Krell, A., & Abele, D. (2011) · doi:10.1002/9781444345988.ch2 · Cited by 10

Coral recruits are highly sensitive to heavy fuel oil exposure both in the presence and absence of UV light

Nordborg, F. M., Brinkman, D. L., & Negri, A. P. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2022.119799 · Cited by 9

Microbiome and Metabolome Contributions to Coral Health and Disease

Schul, M. D., Mason, A. L., Ushijima, B., & Sneed, J. M. (2022) · Biological Bulletin · doi:10.1086/720971 · Cited by 9

Energy Budget for the Cultured, Zooxanthellate Octocoral Sinularia flexibilis

Khalesi, M. K., Beeftink, H. H., & Wijffels, R. H. (2011) · Marine Biotechnology · doi:10.1007/s10126-011-9373-8 · Cited by 9

Cyanobacterial photoprotective compounds: characterization and utilization in human welfare

Sinha, R. P., Pathak, J., Rajneesh, Ahmed, H., Pandey, A., Singh, P. R., Mishra, S., & Häder, D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820655-3.00005-7 · Cited by 9

Ultraviolet Radiation and Aquatic Microbial Ecosystems

Häder, D. (2001) · Springer eBooks · doi:10.1007/978-1-4757-3486-7_6 · Cited by 6

Photoacclimatization in the zooxanthellae of Pocillopora verrucosa and comparison with a pelagic algal community

Maritorena, S., Payri, C. E., Babin, M., Claustre, H., Bonnafous, L., Morel, A., & Rodière, M. (2002) · Oceanologica Acta · doi:10.1016/s0399-1784(02)01189-1 · Cited by 8

UV-absorbing ‘pigments’: mycosporine-like amino acids

Carreto, J. I., Roy, S., Whitehead, K., Llewellyn, C. A., & Carignan, M. O. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511732263.015 · Cited by 7

Electrochemical Characterization of the Marine Antioxidant Gadusol

Arbeloa, E. M., Ramírez, C. L., Procaccini, R. A., & Churio, M. S. (2012) · Natural Product Communications · doi:10.1177/1934578x1200700928 · Cited by 7

UV-protective secondary metabolites from cyanobacteria

Martins, T. P., Arsın, S., Fewer, D. P., & Leão, P. N. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821491-6.00005-3 · Cited by 9

Sunscreens of red algae from Patagonia: a biotechnological perspective

Navarro, N. P. (2015) · Pure and Applied Chemistry · doi:10.1515/pac-2015-0406 · Cited by 7

UV-screening from microalgae

Morocho‐Jácome, A. L., Cezare-Gomes, E. A., de Carvalho, J. C. M., Sauce, R., Rosado, C., Velasco, M. V. R., & Baby, A. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818536-0.00023-3 · Cited by 9

Photoinduced conductivity in mycosporine-like amino acids

Kulkarni, A., Lee, J. H., Seo, H. H., Kim, H.-S., Cho, M. J., Shin, D. S., Kim, T., & Moh, S. H. (2014) · Materials Chemistry and Physics · doi:10.1016/j.matchemphys.2014.11.056 · Cited by 7

Mycosporine-like amino acids in azooxanthellate and zooxanthellate early developmental stages of the soft coral Heteroxenia fuscescens

Ben-Yosef, D., Kashman, Y., & Benayahu, Y. (2008) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2007.11.010 · Cited by 7

Temporal Variation in Photosynthetic Pigments and UV-Absorbing Compounds in Shallow Populations of Two Hawaiian Reef Corals

Kuffner, I. B. (2005) · Pacific Science · doi:10.1353/psc.2005.0048 · Cited by 7

Impact of UV Radiation on Rice-Field Cyanobacteria: Role of Photoprotective Compounds

Sinha, R. P., & Häder, D. P. (2006) · NATO science series. Series IV, Earth and environmental sciences · doi:10.1007/1-4020-3697-3_17 · Cited by 7

Properties of cyanobacterial UV-absorbing pigments suggest their evolution was driven by optimizing photon dissipation rather than photoprotectionPreprint

Simeonov, A., & Michaelian, K. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1702.03588 · Cited by 7

Ultraviolet radiation and primary productivity in temperate aquatic environments of Patagonia (Argentina)

Villafañe, V. E. (2004) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 6

Photoprotective mycosporine-like amino acids in different organs of Baltic flatfish species revealed by targeted and untargeted metabolomics analyses

Hammerle, F. J., Schöpf, R., Karg, C. A., Krumme, U., Gostner, J. M., Karsten, U., & Ganzera, M. (2025) · Frontiers in Marine Science · doi:10.3389/fmars.2025.1688685 · Cited by 7

Effects of aromatic hydrocarbons and evaluation of oil toxicity modelling for larvae of a tropical coral

Nordborg, F. M., Brinkman, D. L., Fisher, R., Parkerton, T. F., Oelgemöller, M., & Negri, A. P. (2023) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2023.115610 · Cited by 6

Effects of UV radiation on seaweeds

Hanelt, D., Wiencke, C., & Bischof, K. (2007) · Springer eBooks · doi:10.1007/978-3-540-48514-8_15 · Cited by 6

Effects of Ultraviolet Radiation ( UV ‐A+ UV ‐B) on the Antioxidant Metabolism of the Red Macroalga Species Acanthophora spicifera (Rhodophyta, Ceramiales) From Different Salinity and Nutrient Conditions

Pereira, D. T., Pereira, B., Fonseca, A. L. D. O., Ramlov, F., Maraschin, M., Álvarez‐Gómez, F., Figueroa, F. L., Schmidt, É. C., Bouzon, Z. L., & Simioni, C. (2019) · Photochemistry and Photobiology · doi:10.1111/php.13094 · Cited by 5

Coral Conservation from the Genomic Perspective on Symbiodiniaceae Diversity and Function in the Holobiont

Shah, S., Dougan, K. E., Bhattacharya, D., & Chan, C. X. (2022) · Coral reefs of the world · doi:10.1007/978-3-031-07055-6_6 · Cited by 5

New Strategies for Identifying Natural Products of Ecological Significance from Corals

(2014) · Studies in natural products chemistry · doi:10.1016/b978-0-444-63430-6.00010-2 · Cited by 5

Impact of UV Radiation on the Aquatic Environment

Häder, D. P. (2006) · NATO science series. Series IV, Earth and environmental sciences · doi:10.1007/1-4020-3697-3_14 · Cited by 5

Coral Reef Biodiversity in the Face of Climatic Changes

La, S. (2011) · InTech eBooks · doi:10.5772/25049 · Cited by 4

Effect of Solar Irradiances on Growth and Pigmentation of Antarctic Red Algae, Kallymenia antarctica and Palmaria decipiens

Han, T., Han, Y., Lee, M., Park, J., Cho, M.-G., Koo, J.-G., & Kang, S. (2003) · Ocean and Polar Research · doi:10.4217/opr.2003.25.4.427 · Cited by 4

Trophic relationships and UV-absorbing compounds in a Mediterranean medio-littoral rocky shore community

Nahon, S., Nozais, C., Delamare‐Deboutteville, J., Escoubeyrou, K., Desmalades, M., Pruski, A. M., Karsten, U., & Charles, F. (2012) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2012.05.009 · Cited by 4

Variación en la concentración de aminoácidos tipo micosporinas en macroalgas de las regiones de Valparaíso y Magallanes, Chile

Velasco‐Charpentier, C., Pizarro‐Mora, F., & Navarro, N. P. (2016) · Revista de biología marina y oceanografía · doi:10.4067/s0718-19572016000300023 · Cited by 4

Ultrastructural Changes of Endosymbiotic Symbiodinium of Galaxea astreata under Thermal Stress and after Short Time Recovery Process

Zhang, Y., Shen, C., Li, F., Shen, Y.-C., & Liu, L. (2018) · Journal of Marine Science Research & Development · doi:10.4172/2155-9910.1000262 · Cited by 4

Short-term variations of mycosporine-like amino acids in the carrageenan-producing red macroalga Mazzaella laminarioides (Gigartinales, Rhodophyta) are related to nitrate availability

Navarro, N., Korbee, N., Jofré, J., & Figueroa, F. (2021) · Journal of Applied Phycology · doi:10.1007/s10811-021-02452-w · Cited by 4

Osmoprotectant and Sunscreen Molecules From Halophilic Algae and Cyanobacteria

Kageyama, H., Waditee‐Sirisattha, R., Tanaka, Y. Y., & Takabe, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-444-63784-0.00001-1 · Cited by 5

Efecto de la radiacion ultravioleta (RUV-A y RUV-B) en la eficiencia fotoquimica y la presencia de micosporinas paraecidas a los aminoacidos (MAAs) en dos corales con simbiontes de filotipo diferente

Barba Santos, M. G. (2004) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

The ultraviolet photobiology of marine phytoplankton

Ward, J. S. (1969)

Mycosporine-like amino acids in phytoplankton: Biochemistry, physiology and optics

Moisan, T. A. H., Goés, J. I., & Neale, P. J. (2015) · Cited by 2

EFFECTS OF ENHANCED SOLAR ULTRAVIOLET RADIATION ON AQUATIC ECOSYSTEMS

Hauder, D., & Worrest, R. C. (1991) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1991.tb08931.x · Cited by 6

Advances in Limnology. Vol. 43. Special Issue: Impact of UVB radiation on pelagic freshwater ecosystems

Häder, D. (1995) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1995.tb02390.x