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Assessing the viability of commercial media for the mass culture of Chaetoceros muelleri

dc.citation.journaltitleThe Philippine Journal of Fisheries
dc.contributor.authorCabanayan-Soy, Rona
dc.contributor.authorde Peralta, Glycinea
dc.contributor.authorJuinio–Meñez, Marie Antonette
dc.date.accessioned2025-06-28T13:46:50Z
dc.date.issued2021-12
dc.descriptionThe authors would like to thank Dr. Rene Abesamis for his valuable comments and the two anonymous reviewers for their suggestions to improve the manuscript. We are also grateful for the guidance of Ms. Elsie Tech in improving the microalgal cultures and providing valuable inputs for this paper. We also thank the Sea Cucumber Research Team and the staff of the University of the Philippines - Marine Science Institute, Bolinao Marine Laboratory for their support and assistance during the conduct of the study. We would also like to acknowledge the Department of Science and Technology Philippine Council for Agriculture, Aquatic and Natural Resources Research and Development (DOST-PCAARRDQSR-MR-CUC.02.02) and the Australian Centre for International Agricultural Research (ACIAR – FIS/2003/059) for the financial support in the conduct of this study.
dc.description.abstractThe microalgae <i>Chaetoceros muelleri</i> is considered a highly nutritious feed for the cultured larvae of the tropical sea cucumber <i>Holothuria scabra</i>. Due to the cost of analytical grade culture media used in the production of <i>C. muelleri</i>, there is a need to evaluate cheap alternative commercial media to decrease the cost of producing quality live microalgal food. In this study, two different indoor batch culture systems (1 L glass bottles and 10 L plastic carboys) were used to evaluate the effectiveness of two conventional (modified F/2 and Walne’s) and one commercial (Epizyme AGP complete) microalgal culture media. Results of the 1 L glass bottle experiment showed that the peak cell density of <i>C. muelleri</i> in AGP (1,241 ± 116 x 10<sup>4</sup> cells ml<sup>-1</sup>) was not significantly different from the modified F/2 (1,584 ± 41 x 10<sup>4</sup> cells ml<sup>-1</sup>) and Walne’s medium (1,319 ± 162 x 10<sup>4</sup> cells ml<sup>-1</sup>) (Kruskal-Wallis test, p=0.78). Likewise, in the plastic carboy experiment, the maximum cell density of <i>C. muelleri</i> in Walne’s medium (750 ± 144 x 10<sup>4</sup> cells ml<sup>-1</sup>) and F/2 medium (653 ± 79 x 10<sup>4</sup> cells ml<sup>-1</sup>) were higher, but not significantly different from AGP (496 ± 184 x 10<sup>4</sup> cells ml<sup>-1</sup>) (Kruskal-Wallis test, p=0.43). The highest growth rate in the glass bottle cultures was the modified F/2 (0.38 div day<sup>-1</sup>), while AGP was the lowest (0.34 div. day<sup>-1</sup>). On the other hand, in carboy culture, AGP was higher (0.17 div.day-1) compared to modified F/2 (0.15 div. day<sup>-1</sup>) and Walne’s medium (0.13 div. day<sup>-1</sup>). The exponential growth phase was similar in the glass bottles, while in the carboy, the exponential phase was reached at a shorter time in the AGP treatment than those in the modified F/2 and Walne’s media. The findings showed that AGP medium is an adequate alternative to replace the conventional media (modified F/2 and Walne’s) during the secondary stock culture for <i>C. muelleri</i>. The viability of using cheaper and more readily available commercial AGP media for the indoor culture production of <i>C. muelleri</i> can contribute to cost-effective scaling-up of the hatchery production of quality <i>H. scabra</i> larvae and early juveniles.
dc.identifier.citationCabanayan-Soy, R., de Peralta, G., & Juinio-Meñez, M. A. (2021). Assessing the viability of commercial media for the mass culture of <i>Chaetoceros muelleri</i>. <i>The Philippine Journal of Fisheries</i>, <i>28</i>(1), 191-199.
dc.identifier.doi10.31398/tpjf/28.2.2019-0007
dc.identifier.issn2672-2836
dc.identifier.issn0048-377X
dc.identifier.urihttps://hdl.handle.net/20.500.14697/605
dc.language.isoen
dc.publisherNational Fisheries Research and Development Institute
dc.relation.urihttps://nfrdi.da.gov.ph/tpjf/etc/Assessing%20the%20Viability%20of%20Commercial%20Media%20for%20the%20Mass%20Culture%20of%20Chaetoceros%20muelleri.pdf
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.agrovocmicroalgae
dc.subject.agrovocaquaculture
dc.subject.agrovocfeeds
dc.subject.agrovoclarvae
dc.subject.agrovocsea cucumbers
dc.subject.agrovocculture media
dc.subject.lcshMicroalgae--Cultures and culture media
dc.subject.lcshLarvae
dc.subject.lcshSea cucumbers
dc.subject.lcshCulture media (Biology)
dc.subject.lcshLive food
dc.subject.odcChallenge 2: Protect and restore ecosystems and biodiversity
dc.subject.odcChallenge 4: Develop a sustainable and equitable ocean economy
dc.subject.sdgSDG 14 - Life below water
dc.subject.sdgSDG 2 - Zero hunger
dc.subject.sdgSDG 12 - Responsible consumption and production
dc.titleAssessing the viability of commercial media for the mass culture of <i>Chaetoceros muelleri</i>
dc.typeArticle
local.subjectHolothuria scabra
local.subjectChaetoceros muelleri
local.subjectculture media viability
local.subjectEpizym-AGP complete medium
local.subject.scientificnameHolothuria scabra
local.subject.scientificnameChaetoceros muelleri
oaire.citation.endPage199
oaire.citation.issue1
oaire.citation.startPage191
oaire.citation.volume28

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