Linking Environmental Factors to Phenolic Concentrations in Seagrasses of Silliman Beach and Olympia Island, Negros Oriental
DOI:
https://doi.org/10.59120/drj.v17i2.548Keywords:
Negros Oriental, phenolics, seagrass, stress bioindicatorAbstract
Seagrass meadows are essential in sustaining marine biodiversity, supporting fisheries, and protecting shorelines. Despite their importance, seagrasses are increasingly exposed to multiple stressors, including sedimentation, nutrient enrichment, pollution, and coastal development. These pressures can trigger biochemical responses such as the accumulation of phenolic compounds. In this study, phenolic concentrations in seagrasses were quantified, and the environmental factors influencing their concentration were identified. Seagrass samples were collected from Silliman Beach (Dumaguete City) and Olympia Island (Bais City), Philippines. Phenolic content was measured using the Folin–Ciocalteu method. Water quality parameters were monitored twice monthly from July 2024 to April 2025, and sediment nutrient analyses were conducted monthly. Results revealed lower phenolic concentrations in the seagrasses at Olympia Island (5.24 to 26.50 mg TAE/g) than at Silliman Beach (6.82 to 50.5 mg TAE/g). Syringodium isoetifolium exhibited the highest phenolic concentration at Silliman Beach, followed by Thalassia hemprichii, Cymodocea rotundata, and Halodule pinifolia. Enhalus acoroides showed the lowest concentrations in both Silliman Beach and Olympia Island. Canonical correspondence analysis showed that phosphorus primarily influenced phenolic accumulation in Syringodium isoetifolium. In other seagrass species, total suspended solids, total dissolved solids, and nutrients correlated with the phenolic concentrations. Increased phenolic production in seagrasses reflects adaptive stress responses and resource allocation toward defense. Therefore, phenolic levels should be incorporated as a biomarker to monitor ecosystem health and guide conservation strategies in Philippine seagrass habitats.
Downloads
References
American Public Health Association, American Water Works Association, & Water Environment Federation. (2017). Standard methods for the examination of water and wastewater (23rd ed.). APHA / AWWA / WEF.
Baby, L., Sankar, T.V., Chandramohanakumar, N., (2017). Changes in phenolic compounds in seagrasses against changes in the ecosystem. Journal of Pharmacognosy and Phytochemistry, 6(3): 742-747
Balogun, S.O., da Silva, Jr. I.F., Colodel, E.M., de Oliveira, R.G., Ascencio, S.D., de Oliveira Martins, D.T. (2014). Toxicological evaluation of hydroethanolic extract of Helicteres sacarolha A. St.- Hil. et al. Journal of Ethnopharmacology, 157, 285-291. https://doi.org/10.1016/j.jep.2014.09.013
Bruckner, M. Z. (2007). Measuring lake turbidity using a Secchi disk. Science Education Resource Center at Carleton College, Montana State University. Microbial Life Educational Resources.https://serc.carleton.edu/microbelife/research_methods/environ_sampling/turbidity.html
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Rica D. Bantoto, TJ G. Alcala, Levi Shane C. Montano, Venus B. Kinamot

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
DRJ is an open-access journal and the article's license is CC-BY-NC. This license allows others to distribute, remix, tweak, and build on the author's work, as long as they give credit to the original work. Authors retain the copyright and grant the journal/publisher non-exclusive publishing rights with the work simultaneously licensed under a https://creativecommons.org/licenses/by-nc/4.0/.
