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Shell powder as source of calcium in the development of Gelidium floridanum (Rhodophyta, Gelidiales) tetraspores and explants

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Abstract

This work aimed to improve the techniques for cultivating the species Gelidium floridanum, testing different sources of calcium. Tetraspores and explants were grown in the laboratory for 20 days with seawater enriched with 50% von Stosch solution and oyster or mussel shell powder (252 mg L-1 and 336 mg L-1), or calcium chloride (147 mg L-1 and 295 mg L-1). Tetraspores or explants cultivated with no calcium salts or shell powder were used as control. Tetraspore germination rate and morphology, and germling morphology, average length, and growth rate were evaluated. Besides, the morphology, upright axes formation and growth rate of explants were also evaluated. There was no difference in tetraspore germination among treatments and control. Treatments with shell powder impaired tetraspore viability, indicated by a greenish color, cellular disorganization, and delay in germ tube development. Germlings cultivated with CaCl2 show better initial development but with no improvement compared to control. Concerning explants, those cultivated with mussel shell powder showed the highest growth rate (3.92 and 4.28% day-1, according to concentration) in relation to other treatments. In particular, those cultivated with 252 mg L-1 mussel shell powder had a significant formation of upright axes (10.15 ± 0.85 upright axes) compared to the control (5.18 ± 0.42 upright axes). Based on these results, we recommend using mussel shell powder at a concentration of 252 mg L-1 to optimize explant cultivation.

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Data Availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

References

  • Aken ME, Griffin NJ, Robertson BL (1993) Cultivation of agarophyte Gelidium pristoides in Algoa Bay. South Africa Hydrobiologia 268:169–178

    Article  CAS  Google Scholar 

  • Altamirano M, Flores-Moya F, Kuhlenkamp R, Figueroa FL (2003) Stage-dependent sensitivity to ultraviolet radiation in zygotes of the brown alga Fucus serratus. Zygote 11:101–106

    Article  CAS  Google Scholar 

  • Armisén R (1991) Agar and agarose biotechnological applications. Hydrobiologia 221:157–166

    Article  Google Scholar 

  • Bouvie F (2018) Effects of extracellular calcium on the Gelidium floridanum germination. Dissertation. Universidade Federal de Santa Catarina, Brazil. (in Portuguese). P 64.

  • Bouzon ZL, Ouriques LO, Oliveira EC (2005) Ultrastructure of tetraspore germination in the agar-producing seaweed Gelidium floridanum (Gelidiales, Rhodophyta). Phycologia 44:409–415

    Article  Google Scholar 

  • Bouzon ZL, Ouriques LC, Oliveira EC (2006) Spore adhesion and cell wall formation in Gelidium floridanum (Rhodophyta, Gelidiales). J Appl Phycol 18:287–294

    Article  Google Scholar 

  • Cai G, Cresti M (2010) Microtubule motors and pollen tube growth still an open question. Protoplasma 247:131–143

    Article  Google Scholar 

  • Cárdenas L, Lovy-Wheeler A, Kunkel JG, Hepler PK (2008) Pollen tube growth oscillations and intracellular calcium levels are reversibly modulated by actin polymerization. Plant Physiol 146:1611–1621

    Article  Google Scholar 

  • Derksen J, Rutten T, Amstel TV, Win A, Doris F, Steer M (1995) Regulation of pollen tube growth. Acta Bot Neerl 44:93–119

    Article  Google Scholar 

  • EPAGRI (2019) Annual Summary of Agriculture in Santa Catarina 2018-2019 (In Portuguese). Available at: https://docweb.epagri.sc.gov.br/website_cepa/publicacoes/Sintese_2018_19.pdf (last accessed 20 January 2022)

  • Fei XG, Huang LJ (1991) Artificial sporeling and field cultivation of Gelidium in China. Hydrobiologia 221:119–124

    Article  Google Scholar 

  • Filipin EP, Pereira DT, Ouriques LC, Bouzon ZL, Simioni C (2019) Participation of actin filaments, myosin and phosphatidylinositol 3-kinase in the formation and polarisation of tetraspore germ tube of Gelidium floridanum (Rhodophyta, Florideophyceae). Plant Biol 21:352–360

    Article  CAS  Google Scholar 

  • Fredriksen S, Rueness J (1989) Culture studies of Gelidium latifolium (Grev.) Born. et Thur. (Rhodophyta) from Norway. Growth and nitrogen storage in response to varying photon flux density, temperature and nitrogen availability. Bot Mar 32:539–546

    Article  Google Scholar 

  • Green JJ, Cervantes DC, Peters NT, Logan KO, Kropf DL (2013) Dynamic microtubules and endomembrane cycling contribute to polarity establishment and early development of Ectocarpus mitospores. Protoplasma 250:1035–1043

    Article  CAS  Google Scholar 

  • Hable WE, Hart PE (2010) Signaling mechanisms in the establishment of plant and fucoid algal polarity. Mol Reprod Dev 77:751–758

    Article  CAS  Google Scholar 

  • Hamester MRR, Balzer PS, Becker D (2012) Characterization of calcium carbonate obtained from oyster and mussel shells and incorporation in polypropylene. Mater Res 15:204–208

    Article  CAS  Google Scholar 

  • Hansen JE (1980) Physiological considerations in the mariculture of red algae. J World Mariculture Soc 14:1–4

    Google Scholar 

  • McLachlan J (1973) Growth media-marine. In: Stein JR (ed) Handbook of Phycological methods. Culture Methods and Growth Measurements. Cambridge University Press, Cambridge, pp 25–55

    Google Scholar 

  • Mairh O, Rao P (1978) Culture studies on Gelidium pusillum (Stackh.) Le Jolis. Bot Mar 21:169–174

    Article  Google Scholar 

  • Melo RA, Harger BWW, Neushul M (1991) Gelidium cultivation in the sea. Hydrobiologia 221:91–106

    Article  Google Scholar 

  • Otaíza RD, Cáceres JH, Rodriguez CY, Sanhueza AG (2019) Seeding of fragments of the agarophyte Gelidium lingulatum (Rhodophyta, Gelidiales) for the repopulation of lower levels of wave exposed, intertidal rocky shores. J Appl Phycol 31:2133–2143

    Article  Google Scholar 

  • Porse H, Rudolph B (2017) The seaweed hydrocolloid industry: 2016 updates, requirements, and outlook. J Appl Phycol 29:2187–2200

    Article  Google Scholar 

  • Santelices B (1976) Note on mass cultivation of some species of Gelidiales (Rhodophyta). Rev Biol Mar Oceanogr 16:27–33 (In Spanish)

    Google Scholar 

  • Santelices B (1991) Production ecology of Gelidium. Hydrobiologia 221:31–44

    Article  Google Scholar 

  • Santos R, Melo RA (2018) Global shortage of technical agars: back to basics (resource management). J Appl Phycol 30:2463–2473

    Article  Google Scholar 

  • Simioni C, Schmidt ÉC, Rover T, Santos R, Filipin EP, Pereira DT, Costa GB, Oliveira ER, Chow F, Ramlov F, Ouriques L, Maraschin M, Bouzon ZL (2015) Effects of cadmium metal on young gametophytes of Gelidium floridanum: metabolic and morphological changes. Protoplasma 252:1347–1359

    Article  CAS  Google Scholar 

  • Veeragurunathan V, Vadodariya N, Chaudhary JP, Gogda A, Saminathan KR, Meena R (2018) Experimental cultivation of Gelidium pusillum in open sea along the south east Indian coast. Indian J Geo Mar Sci 47:336–345

    Google Scholar 

  • Yarish C, Pereira R (2008) Mass production of marine macroalgae. In: Jørgensen SE, Fath BD (eds) Encyclopedia of ecology. Elsevier, Oxford, pp 2236–2247

    Google Scholar 

  • Yokoya NS, Handro W (1997) Thallus regeneration and growth induced by plant growth regulators and light intensity in Grateloupia dichotoma (Rhodophyta). In: Kitamura T (ed) Proceedings of the I.T.I.T. International Symposium on New Technologies from Marine-Sphere, Kagawa, Japan, pp 83–86

  • Zhou W, Sui Z, Wang J, Hu Y, Kang KH, Hong HR, Niaz Z, Wei H, Du Q, Peng C, Mi P, Que Z (2016) Effects of sodium bicarbonate concentration on growth, photosynthesis, and carbonic anhydrase activity of macroalgae Gracilariopsis lemaneiformis, Gracilaria vermiculophylla, and Gracilaria chouae (Gracilariales, Rhodophyta). Photosynth Res 128:259–270

    Article  CAS  Google Scholar 

Download references

Acknowledgments

CPB thanks Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina (FAPESC) for the master's scholarship. LH thanks Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the Productivity Fellowship (Process number 311680/2020-8). This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001. We also thanks Fernando Zwierzikowski da Silva for the technical support and Prof. Zenilda L. Bouzon for the Plant Cell Biology Laboratory infrastructure.

Funding

This work was funding by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001, Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina (FAPESC) for the master's scholarship of Camila Pereira Bruzinga and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the Productivity Fellowship (Process number 311680/2020-8) of Leila Hayashi.

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Correspondence to Leila Hayashi.

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Bruzinga, C.P., Simioni, C. & Hayashi, L. Shell powder as source of calcium in the development of Gelidium floridanum (Rhodophyta, Gelidiales) tetraspores and explants. J Appl Phycol 34, 2579–2588 (2022). https://doi.org/10.1007/s10811-022-02796-x

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  • DOI: https://doi.org/10.1007/s10811-022-02796-x

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