Abstract
Increase of harmful radiation to the Earth’s surface due to ozone depletion results in higher exposure to harmful ultraviolet- B radiation (UV), while fluctuations in seawater salinity may alter water density, ionic concentration, nutrient uptake, and osmotic pressure. This study evaluated the effects of salinity and UV on metabolism and morphology of Acanthophora spicifera (M.Vahl) Børgesen. Water with 30 and 37 psu [g(salt) kg–1(sea water)] was used for experiments during 7 d of exposure to UV (3 h per day). We demonstrated that UV treatment predisposed, irrespective of salinity, A. spicifera to a decrease in its growth rate and cell viability, as well as affected its morphological parameters. After exposure to PAR + UVA + UVB (PAB), samples showed structural changes and damage, such as increasing cell wall thickness and chloroplast disruption. Our results indicate that UV led to dramatic metabolic changes and cellular imbalances, but more remarkable changes were seen in samples exposed to high salinity.
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Abbreviations
- ANOVA:
-
analysis of variance
- BSA:
-
bovine serum albumin
- CW:
-
cell wall
- C:
-
chloroplast
- CC:
-
cortical cells
- cyt c :
-
cytochrome complex
- DM:
-
dry mass
- FM:
-
fresh mass
- GR:
-
growth rates
- HCA:
-
hierarchical clustering analysis
- IPCC:
-
Intergovernmental Panel on Climate Change
- LM:
-
light microscopy
- MCW:
-
methanol:chloroform:water
- M:
-
mitochondria
- MTP:
-
mitochondrial transmembrane potential
- N:
-
nucleus
- PAB:
-
PAR + UVA + UVB
- P:
-
plastoglobuli
- PCA:
-
principal component analysis
- psu:
-
practical salinity unit [g(salt) kg–1(sea water)]
- ROS:
-
reactive oxygen species
- SD:
-
standard deviation
- S:
-
starch grains
- SC:
-
subcortical cells
- TB-O:
-
toluidine blue
- TEM:
-
transmission electron microscopy
- UVA:
-
UV A radiation
- UVB:
-
UV B radiation
- UVC:
-
UV C radiation
References
Aguilera J., Karsten U., Lippert H. et al.: Effects of solar radiation on growth, photosynthesis and respiration of marine macroalgae from the Arctic.–Mar. Ecol.-Prog. Ser. 191: 109–119, 1999.
Aminot A., Chaussepied M.: [Manual of Chemical Analyzes in Marine Environment.] Pp. 379. CNEXO, Brest 1983. [In French]
Araújo F.O., Ursi S., Plastino E.M.: Intraspecific variation in Gracilaria caudata (Gracilariales, Rhodophyta): growth, pigment content, and photosynthesis.–J. Appl. Phycol. 26: 849–858, 2014.
Baghel R.S., Kumari P., Reddy C.R.K., Jha B.: Growth, pigments, and biochemical composition of marine red alga Gracilaria crassa.–J. Appl. Phycol. 26: 2143–2150, 2014.
Balogh T.S., Velasco M.V.R., Pedriali C.A. et al.: [Protection against ultraviolet radiation: features currently available under photoprotection.]–Ann. Bras. Dermatol. 86: 732–42, 2011. [In Portuguese]
Baltruschat H., Fodor J., Harrach B.D. et al.: Salt tolerance of barley induced by the root endophyte Piriformospora indica is associated with a strong increase in antioxidants.–New Phytol. 180: 501–510, 2008.
Barros M.P., Necchi O., Colepicolo P. et al.: Kinetic study of the plastoquinone pool availability correlated with H2O2 release in seawater and antioxidant responses in the red alga Kappaphycus alvarezii exposed to single or combined high light, chilling and chemical stresses.–BBA-Bioenergetics 1757: 1520–1528, 2006.
Bartley M.L., Boeing W.J., Corcoran A.A. et al.: Effects of salinity on growth and lipid accumulation of biofuel microalga Nannochloropsis salina and invading organisms.–Biomass Bioenerg. 54: 83–88, 2013.
Batista R.D., Batista R.D., Santos G.R. et al.: [Antioxidative responses in cowpea nodules inoculated with bradyrhizobium.]–Desafios 2: 76–88, 2015. [In Portuguese]
Berridge M.V., Herst P.M., Tan A.S.: Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction.–Biotechnol. Annu. Rev. 11: 127–152, 2005.
Biever, J.J., Brinkman D., Gardner G.: UV-B inhibition of hypocotyl growth in etiolated Arabidopsis thaliana seedlings is a consequence of cell cycle arrest initiated by photodimer accumulation.–J. Exp. Bot. 65: 2949–2961, 2014.
Bischof K., Hanelt D., Wiencke C.: Effects of ultraviolet radiation on photosynthesis and related enzyme reactions marine macroalgae.–Planta 211: 555–562, 2000.
Bischof K., Kräbs G., Wiencke C. et al.: Solar ultraviolet radiation affects the activity of ribulose-1, 5-bisphosphate carboxylase-oxygenase and the composition of photosynthetic and xanthophyll cycle pigments in the intertidal green alga Ulva lactuca L.–Planta 215: 502–509, 2002.
Borderie F., Laurence A.S., Naoufal R. et al.: UV-C irradiation as a tool to eradicate algae in caves.–Int. Biodeter. Biodegr. 65: 579–584, 2011.
Bradford M.M.: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.–Anal. Biochem. 72: 248–254, 1976.
Cavalcanti F.R., Lima J.P.M., Ferreira-Silva S.L. et al.: Roots and leaves display contrasting oxidative response during salt stress and recovery in cowpea.–J. Plant Physiol. 164: 591–600, 2007.
Choo K.S., Snoeijs P., Pedersén M.: Oxidative stress tolerance in the filamentous green algae Cladophora glomerata and Enteromorpha ahlneriana.–J. Exp. Mar. Biol. Ecol. 298: 111–123, 2004.
Chow F., Macchiavello J., Cruz S.S. et al.: Utilization of Gracilaria chilensis (Rhodophyta: Gracilariaceae) as a biofilter in the depuration of effluents from tank cultures of fish, oysters, and sea urchins.–J. World Aquacult. Soc. 32: 2515–220, 2001.
Chow F.: Nitrate assimilation: the role of in vitro nitrate reductase assay as nutritional predictor.–In: Najafpour M.M. (ed.): Applied Photosynthesis. Pp. 105–120. In Tech, Croatia 2012.
Connan S., Stengel D.B.: Impacts of ambient salinity and copper on brown algae: 2. Interactive effects on phenolic pool and assessment of metal binding capacity of phlorotannin.–Aquat. Toxicol. 104: 1–13, 2011.
Costa V.M.F.: [Use of the macroalgae Ulva lactuca Linnaeus in nutrient reduction (NH4+, NO3–e PO–24) from shrimp farming.]–PhD Thesis, Federal University of Rio Grande do Norte, 2006. [In Portuguese]
Cronin G., Lodge D.M.: Effects of light and nutrient availability on the growth, allocation, carbon/nitrogen balance, phenolic chemistry, and resistance to herbivory of two freshwater macrophytes.–Oecologia 137: 32–41, 2003.
Dailer M.L., Smith J.E., Smith C.E.: Responses of bloom forming and non-bloom forming macroalgae to nutriente enrichment in Hawaii, USA.–Harmful Algae 17: 111–125, 2012.
de Almeida S.L., Schmidt E.C., Pereira D.T. et al.: Effect of ultraviolet-B radiation in laboratory on morphological and ultrastructural characteristics and physiological parameters of selected cultivar of Oryza sativa L.–Protoplasma 250: 1303–1313, 2013.
de Azevedo Neto A.D., Prisco J.T., Enéas-Filho J. et al.: Effect of salt stress on antioxidative enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes.–Environ. Exp. Bot. 56: 87–94, 2006.
de Reviers B.: [Biology and Phylogeny of Algae. 2nd ed.] Pp. 280. Artmed, Brazil 2006. [In Portuguese]
De Tullio M.C.: Antioxidants and redox regulation: Changing notions in a changing world.–Plant Physiol. Bioch. 48: 289–291, 2010.
Devi M.P., Subhash G.V., Mohan S.V.: Heterotrophic cultivation of mixed microalgae for lipid accumulation and wastewater treatment during sequential growth and starvation phases: effect of nutrient supplementation.–Renew. Energ. 43: 276–283, 2012.
Diffey B.L.: Sources and measurement of ultraviolet radiation.–Methods 28: 4–13, 2002.
Duarte M.E., Cauduro J.P., Noseda D.G. et al.: The structure of the agaran sulfate from Acanthophora spicifera (Rhodomelaceae, Ceramiales) and its antiviral activity. Relation between structure and antiviral activity in agarans.–Carbohydr. Res. 339: 335–347, 2004.
Edwards P.: Cultured red alga to measure pollution.–Mar. Pollut. Bull. 3: 184–188, 1972.
Felix M.R., Osorio L.K., Ouriques L.C. et al.: The effect of cadmium under different salinity conditions on the cellular architecture and metabolism in the red alga Pterocladiella capillacea (Rhodophyta, Gelidiales).–Microsc. Microanal. 20: 1411–1424, 2014.
Fialho F.A.N.: [Integrated multitrophic aquaculture: macroalgae biofilters in the culture of the arrowhead.]–Completion of course work of the Federal University of Santa Catarina, 2013. [In Portuguese]
Fidantsef A.L., Britt A.B.: Preferential repair of the transcribed DNA strand in plants.–Front. Plant Sci. 2: 105, 2012.
Figueroa F.L., Domínguez-González B., Korbee N.: Vulnerability and acclimation to increased UVB radiation in three intertidal macroalgae of different morpho-functional groups.–Mar. Environ. Res. 97: 30–38, 2014.
Fong P., Boyer K.E., Desmond J.S., Zedler J.B.: Salinity stress, nitrogen competition, and facilitation: what controls seasonal succession of two opportunistic green macroalgae?–J. Exp. Mar. Biol. Ecol. 206: 203–221, 1996.
Forzza R.C., Baumgratz J.F.A., Bicudo C.E.M. et al.: New Brazilian floristic list highlights conservation challenges.–BioScience 62: 39–45, 2012.
Franceschini I. M., Burliga A. L., de Reviers B. et al.: [Algae: a phylogenetic, taxonomic and ecological approach.] Pp. 19–57. Artmed, Brazil 2010. [In Portuguese]
Fukayama H., Ueguchi C., Nishikawa K. et al.: Overexpression of Rubisco activase decreases the photosynthetic CO2 assimilation rate by reducing Rubisco content in rice leaves.–Plant Cell Physiol. 53: 976–986, 2012.
Ganesan P., Kumar C.S., Bhaskar N.: Antioxidant properties of methanol extract and its solvent fractions obtained from selected Indian red seaweeds.–Bioresour. Technol. 99: 2717–2723, 2008.
Gill S.S., Tuteja N.: Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants.–Plant Physiol. Bioch. 48: 909–930, 2010.
Gómez I., Huovinen P.: Morpho-functional patterns and zonation of South Chilean seaweeds: the importance of photosynthetic and bio-optical traits.–Mar. Ecol. Prog. Ser. 422: 77–91, 2011.
Gordon E.M., McCandless E.L.: Ultrastructure and histochemistry of Chondrus crispus Stackhouse.–Nova Scotia Inst. Sci. Proc. 27: 111–133, 1973.
He Y.Y., Häder D.P.: Reactive oxygen species and UV-B: effect on cyanobacteria.–Photoch. Photobio. Sci. 1: 729–736, 2002.
Heo S.J., Ko S.C., Kang S.M. et al.: Cytoprotective effect of fucoxanthin isolated from brown algae Sargassum siliquastrum against H2O2-induced cell damage.–Eur. Food Res. Technol. 228: 145–151, 2008.
Heo S.J., Ko S., Kang S. et al.: Inhibitory effect of diphlorethohydroxycarmalol on melanogenesis and its protective effect against UV-B radiation-induced cell damage.–Food Chem. Toxicol. 48: 1355–1361, 2010.
Holzinger A., Lütz C.: Algae and UV irradiation: effects on ultrastructure and related metabolic functions.–Micron 37: 190–207, 2006.
Horn R.A.: The effect of litopenaeus stylirostris aquaculture on macroalgae growth in opunohu Bay, moorea, French polynesia.–Stud. Res. Papers 1: 1–12, 2012.
Ifeanyi V.O., Anyanwu B.N., Ogbulie J.N. et al.: Determination of the effect of light and salt concentrations on Aphanocapsa algal population.–Afr. J. Microbiol. Res. 5: 2488–2492, 2011.
Jayasankar R.: Effect of salinity on physiology of Gracilaria spp. (Gigartinales, Rhodophyta).–Seaweed Res. Util. 27: 19–24, 2005.
Jormalainen V., Honkanen T., Koivikko R. et al.: Induction of phlorotannin production in a brown alga: defense or resource dynamics?–Oikos 103: 640–650, 2003.
Kalbina I., Strid A.: The role of NADPH oxidase and MAP kinase phosphatase in UV-B-dependent gene expression in Arabidopsis.–Plant Cell Environ. 29: 1783–1793, 2006.
Lang K.L.: [Chemical and biological research of red algae Acanthophora spicifera (Vahl) Borgesen.]–PhD. Thesis of Federal University of Santa Catarina, 2006. [In Portuguese]
Li X., Zhang L., Li Y. et al.: Changes in photosynthesis, antioxidant enzymes and lipid peroxidation in soybean seedlings exposed to UV-B radiation and/or Cd.–Plant Soil 352: 377–387, 2012.
Lin C.C., Kao C.H.: Cell wall peroxidase activity, hydrogen peroxide level and NaCl-inhibited root growth of rice seedlings.–Plant Soil 230: 135–143, 2001.
Lobban C.S., Harrison P.J.: Temperature and salinity.–In: Lobban C.S., Harrison P.J. (ed.): Seaweed Ecology and Physiology. Pp. 210–240. Cambridge Univ. Press, Cambridge 1994.
Macler B.A.: Salinity effects on photosynthesis, carbon allocation, and nitrogen assimilation in the red alga, Gelidium coulteri.–Plant Physiol. 88: 690–694, 1988.
Madronich S.: Implications of recent total atmospheric ozone measurements for biological active ultraviolet radiation reaching the Earth’s surface.–Geophys. Res. Let. 19: 37–40, 1992.
Maia J.M., Ferreira-Silva S.L., Voigt E.L. et al.: [Activity of antioxidant enzymes and inhibition of root growth of cowpea under different levels of salinity.]–Acta Bot. Bras. 26: 342–349, 2012. [In Portuguese]
Mallick N., Mohn F.H.: Reactive oxygen species: response of algal cells.–J. Plant Physiol. 157: 183–193, 2000.
Mandal S.K., Ajay G., Monisha N. et al.: Differential response of varying temperature and salinity regimes on nutrient uptake of drifting fragments of Kappaphycus alvarezii: implication on survival and growth.–J. Appl. Phycol. 27: 1571–1581, 2015.
McCready R.M., Guggolz A., Silveira V. et al.: Determination of starch and amylase in vegetables; application to peas.–Anal. Chem. 22: 1156–1158, 1950.
Mendes L.F., Zambotti-Villela L., Colepicolo P. et al.: Metal cation toxicity in the alga Gracilaria domingenses as evaluated by the daily growth rates in synthetic seawater.–J. Appl. Phycol. 25: 1939–1947, 2013.
Mitchell D.L., Jen J., Cleaver J.E.: Sequence specificity of cyclobutane pyrimidine dimers in DNA treated with solar (ultraviolet-B) radiation.–Nucleic Acids Res. 20: 225–229, 1992.
Mittova V., Guy M., Tal M. et al.: Salinity up-regulates the antioxidative system in root mitochondria and peroxisomes of the wild salt-tolerant tomato species Lycopersicon pennellii.–J. Exp. Bot. 55: 1105–1113, 2004.
Mittler R., Vanderauwera S., Suzuki N. et al.: ROS signalling: The new wave?–Trends Plant Sci. 16: 300–309, 2011.
Mosmann T.: Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays.–J. Immunol. Methods 65: 55–63, 1983.
Murphy J., Riley J.P.: A modified single solution method for the determination of phosphate in natural waters.–Anal. Chim. Acta 27: 31–36, 1962.
Navarro N.P., Mansilla A., Plastino E.M.: Iridaea cordata (Gigartinales, Rhodophyta): responses to artificial UVB radiation.–J. Appl. Phycol. 22: 385–394, 2010.
Navarro N.P., Mansilla A., Figueroa F.L. et al.: Short-term effects of solar UVradiation and NO3- supply on the accumulation of mycosporine-like amino acids in Pyropia columbina (Bangiales, Rhodophyta) under spring ozone depletion in the sub-Antarctic region.–Chile Bot. Mar. 57: 9–20, 2014.
Nawkar G.M., Maibam P., Park J.H. et al.: UV-induced cell death in plants.–Int. J. Mol. Sci. 14: 1608–1628, 2013.
Nejrup L.B., Pedersen M.F.: The effect of temporal variability in salinity on the invasive red alga Gracilaria vermiculophylla.–Eur. J. Phycol. 47: 254–263, 2012.
Nitschke U., Karsten U., Eggert A.: Physiological performance of the red alga Stylonema alsidii (Stylonematophyceae) under varying salinities.–J. Exp. Mar. Biol. Ecol. 460: 170–176, 2014.
Penniman C.A., Mathieson A.C., Penniman C.E.: Reproductive phenology and growth of Gracilaria tikvahien McLachlan (Gigartiales, Rhodophyta) in the Great Bay Estuary, New Hampshire.–Bot. Mar. 29: 147–154, 1986.
Pereira D.T., Schmidt E.C., Bouzon Z.L. et al.: The effects of ultraviolet radiation-B response on the morphology, ultrastructure, and photosynthetic pigments of Laurencia catarinensis and Palisada flagellifera (Ceramiales, Rhodophyta): a comparative study.–J. Appl. Phycol. 26: 2443–2452, 2014.
Pérez-Rodríguez E., Gómez I., Karsten U., Figueroa F.L.: Effects of UV radiation on photosynthesis and excretion of UVabsorbing compounds of Dasycladus vermicularis (Dasycladales, Chlorophyta) from southern Spain.–Phycologia 37: 379–387, 1998.
Polo L.K., Feliz M.R., Kreusch M. et al.: Photoacclimation responses of the brown macroalga Sargassum Cymosum to the combined influence of UV radiation and salinity: cytochemical and ultrastructural organization and photosynthetic performance.–J. Photoch. Photobio. 90: 560–573, 2014.
Polo L.K., Felix M.R., Kreusch M. et al.: Metabolic profile of the brown macroalga Sargassum cymosum (Phaeophyceae, Fucales) under laboratory UVradiation and salinity conditions.–J. Appl. Phycol. 27: 887–899, 2015.
Poppe F., Hanelt D., Wiencke C.: Changes in ultrastructure, photosynthetic activity and pigments in the Antarctic red alga Palmaria decipiens during acclimation to UV radiation.–Bot. Mar. 45: 253–261, 2002.
Poppe F., Schmidt R.A., Hanelt D. et al.: Effects of UVradiation on the ultrastructure of several red algae.–Phycol. Res. 51: 11–19, 2003.
Rao M. V, Paliyath G., Ormrod P.: Ultraviolet-B- and ozoneinduced biochemical changes in antioxidant enzymes of Arabidopsis thaliana.–Plant Physiol. 110: 125–36, 1996.
Recuenco-Muñoz L., Offre P., Valledor L. et al.: Targeted quantitative analysis of a diurnal RuBisCO subunit expression and translation profile in Chlamydomonas reinhardtii introducing a novel Mass Western approach.–J. Proteomics 113: 143–153, 2015.
Rojas M.O.A.I., Neto J.J.C.G., Barbiere R.: [Physical-chemical evaluation of the water of the Jansen Lagoon, São Luis, MA.]–Acta Tecnol. 8: 19–24, 2013. [In Portuguese]
Roleda M.T., Hanelt D., Kräbs G. et al.: Morphology, growth, photosynthesis and pigmentes in Laminaria ochroleuca (Laminariales, Phaeophyta) under ultraviolet radiation.–Phycology 43: 603–613, 2004.
Scherner F., Ventura R., Barufi J.B., Horta P.A.: Salinity critical threshold values for photosynthesis of two cosmopolitan seaweed species: providing baselines for potential shifts on seaweed assemblages.–Mar. Environ. Res. 91: 14–25, 2013.
Schmidt E.C., Scariot L.A., Rover T., Bouzon Z.L.: Changes in ultrastructure and histochemistry of two red macroalgae strains of Kappaphycus alvarezii (Rhodophyta, Gigartinales), as a consequence of ultraviolet B radiation exposure.–Micron 40: 860–869, 2009.
Schmidt E.C., Nunes B.G., Maraschin M. et al.: Effect of ultraviolet-B radiation on growth, photosynthetic pigments, and cell biology of Kappaphycus alvarezii (Rhodophyta, Gigartinales) macroalgae brown strain.–Photosynthetica 48: 161–172, 2010.
Schmidt E.C., dos Santos R.W., Faveri C. et al.: Response of the agarophyte Gelidium floridanum after in vitro exposure to ultraviolet radiation B: changes in ultrastructure, pigments, and antioxidant systems.–J. Appl. Phycol. 24: 1341–1352, 2012.
Shannon J.C.: A procedure for the extraction and fractionation of carbohydrates from immature Zea mays kernels.–Res. Bull. 842: 1–8, 1968.
Simioni C., Rover T, Schmidt E.C. et al.: Effects of brefeldin A on the endomembrane system and germ tube formation of the tetraspore of Gelidium floridanum (Rhodophyta, Florideophyceae).–J. Phycol. 50: 577–586, 2014.
Souza-Mosimann R.M., Laudares-Silva R., Talgatti D.M. et al.: The diatom flora in Conceição Lagoon, Florianópolis, SC, Brazil.–Insula Rev. Bot. Florianópolis 40: 25–54, 2011.
Sutherland B.M., Takayanagi S., Sullivan J.H., Sutherland J.C.: Plant responses to changing environmental stress: cyclobutyl pyrimidine dimer repair in soybean leaves.–Photochem. Photobiol. 64: 464–468, 1996.
Takagi M., Karseno, Yoshida T.: Effect of salt concentration on intracellular accumulation of lipids and triacylglyceride in marine microalgae Dunaliella cells.–J. Biosci. Bioeng. 101: 223–226, 2006.
Umbreit W.W., Burris R.H.: Method for Glucose Determination and other Sugars. Manome-tric Techniques, 4th ed. Pp. 338. Burgess Publishing Co., London 1964.
van de Poll W.H., Hanelt D., Hoyer K. et al.: Ultraviolet-Binduced cyclobutane-pyrimidine dimer formation and repair in arctic marine macrophytes.–Photochem. Photobiol. 76: 493–500, 2002.
Wang C., Mingyan W., Jingyu S. et al.: Research on the chemical constituents of Acanthophora spicifera in the South China Sea.–Chin. J. Magn. Reson. 15: 237–242, 1998.
Wiencke C., ómez I., Pakker H. et al.: Impact of UVradiation on viability, photosynthetic characteristics and DNA on algal zoospores: implications for depth zonation.–Mar. Ecol. Progr. Ser. 197: 217–219, 2000.
Yao N., Eisfelder B.J., Marvin J. et al.: The mitochondrion-an organelle commonly involved in programmed cell death in Arabidopsis thaliana.–Plant J. 40: 596–610, 2004.
Zakaria N.A., Darah I., Shaida F.S. et al.: Phytochemical composition and antibacterial potential of hexane extract from malaysian red algae, Acanthophora spicifera (Vahl) Borgesen.–World Appl. Sci. J. 15: 496–501, 2011.
Zhao J., Li L.: Effects of UV-B irradiation on isoforms of antioxidant enzymes and their activities in red alga Grateloupia filicina (Rhodophyta).–Chin. J. Oceanol. Limnol. 32: 1364–1372, 2014.
Zeng L.M., Chao-Jie W., Jing-Yu S. et al.: Flavonoids from the red alga Acanthophora spicifera.–Chin. J. Chem. 19: 1097–1100, 2001.
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Acknowledgments: The authors would like to acknowledge the staff of the Central Laboratory of Electron Microscopy (LCME), Federal University of Santa Catarina, Florianópolis, SC, Brazil, for the use of their transmission electron microscope. The authors acknowledge the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, Brazil) for the financial support to Éder C. Schmidt (process 473088/2013-4) and Fernanda Ramlov (process 473408/2013-9). Zenilda L. Bouzon is a CNPq Fellow. This study is part of the MSc dissertation of the first author.
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Table 1S. Two-away ANOVA for salinity (30 and 37 psu), treatment (natural, PAR and PAB treatment), and interaction between treatment and salinity for physiological and biochemical parameters of Acanthophora spicifera.
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Pereira, D.T., Simioni, C., Ouriques, L.C. et al. Comparative study of the effects of salinity and UV radiation on metabolism and morphology of the red macroalga Acanthophora spicifera (Rhodophyta, Ceramiales). Photosynthetica 56, 799–810 (2018). https://doi.org/10.1007/s11099-017-0731-2
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DOI: https://doi.org/10.1007/s11099-017-0731-2