Browse > Article
http://dx.doi.org/10.5657/kfas.2003.36.3.225

Viability Assay of Seaweeds Responding to Mountain Fire-Related Pollutants  

KANG Se-Eun (Department of Biotechnology, Pukyong National University)
JIN Long-Guo (Department of Biotechnology, Pukyong National University)
CHOI Jae-Suk (Department of Biotechnology, Pukyong National University)
CHO Ji-Young (Department of Biotechnology, Pukyong National University)
SHIN Hyun-Woung (Department of Marine Biotechnology, Soonchunhyang University)
HONG Yong-Ki (Department of Biotechnology, Pukyong National University)
Publication Information
Korean Journal of Fisheries and Aquatic Sciences / v.36, no.3, 2003 , pp. 225-229 More about this Journal
Abstract
Plant ash and soil drainage, derived by frequent mountain fires during winter, might cause biological contamination to seaweeds at seashore and river mouse area. To thalli of Ulva pertusa, maximum non-lethal concentration(MNLC), lethal concentration 50 $(LC_{50})$ and minimum lethal concentration (MLC) of pine needle ash were shown as 60, 350 and 550 mg/mL, respectively. The yellow loess and granite sand did not damage at concentrations of 20 and 200 mg/mL, respectively To thalli of Porphyra yezoensis, the MNLC, LC5O, MLC of pine needle ash were shown as 0.08, 0.4 and 1.0 mg/mL, respectively. Effects of yellow loess and granite sand were approximately 1/2 and 1/10 of the ash. To thalli of Undaria pinnatifida, the pine needle ash, yellow loess and granite sand did not damage at the concentration range of 20 to 40 mg/mL. Change of pigments $(chlorophyll\;\alpha,\;lutein,\;\beta-carotene,\;phycoerthrin)$ was also determined at the MNLC, $LC-{50}$ and MLC of pine needle ash. Among three seaweeds tested, P. yezoensis produced the most 2.7-fold of lutein and 2.3-fold of $\beta-carotene$ at $LC-{50}$ of the ash. Thus the P. yezoensis, appeared as a sensitive indicator, could be used as one of test organisms for determination of the biological effect of pollutants contaminated in marine environment.
Keywords
Pigment; Pine needle ash; Porphyra yezoensis; Tetrazolium; Ulva pertusa; Undaria pinnatifida; Viability;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Su, X and A. Gibor. 1988. A method for RNA isolation from marine macro-algae. Anal. Biochern., 174, 650- 657   DOI   ScienceOn
2 NFRDI (National Fisheries Research and Development Institute). 2000. A report on the effect of mountain fire occuvred in the East coast on the costal fishing grounds, East Sea Fisherich Institute, Kwibin Publishing Co., Gangneung, Korea, 101 pp
3 Jin, L.G., J.S. Choi, H.J. Jin, H.W. Shin and Y.K. Hong. 2002. Isolation of pollutant (pine needle ash )-responding genes from the seaweed Porphyra yezoensis tissue. Fish. Sci., 68, S1044-S1047   DOI
4 Kim, J.K. and T.J. Han. 2000. Effects of inorganic nutrients and heavy metals on reproduction of the green algae Ulva pertusa Kjellman. Algae, 15, 81-88
5 Leborans, G.F. and A. Novillo. 1996. Toxicity and bioaccumulation of cadmium in Olisthodiscus luteus. Water Res., 30, 56-62
6 Lobban, C.S., D.J. Chapman and B.P. Kremer. 1988. Experimental Phycology: A Laboratory Manual. Cambridge University Press, New York, 295pp
7 ProvasoIi, L. 1966. Media and prospects for the cultivation of marine algae. In: Cultures and Collections of Algae. Watanabe A. and A. Hattori eds., Jap. Soc. Plant Physiol., Tokyo, pp. 63-75
8 Naldi, M. and P.A. Wheeler. 1999. Changes in nitrogen pools in Ulva fenestrata (Chlorophyta) and Gracilaria pacifica (Rhodophyta) under nitrate and ammonium enrichment. J. Phycol., 35, 70-77   DOI   ScienceOn
9 Nam, B.H., H.J. Jin, S.K. Kim and Y.K. Hong. 1998. Quantitative viability of seaweed tissues assessed with 2, 3, 5-triphenyltetrazolium chloride. J. Appl. Phycol., 10, 31-36   DOI   ScienceOn
10 Park, J.W., Y.C. Cho, B.H. Nam, H.J. Jin, C.H. Sohn and Y.K. Hong. 1998. RAPD identification of genetic variation in the seaweed Hizikia fusiformis (Fucales, Phaeophyta). J. Mar. Biotechnol., 6, 62-64
11 Rioboo, C., O. Gonzalez, C. Herrero and A. Cid. 2002. Physiological response of freshwater microalga (Chlorella vulgaris) to triazine and phenylurea herbicides. Aquatic Toxicol., 59, 225-235   DOI   ScienceOn
12 Steidinger, K.A. 1983. A re-evaluation of toxic dinoflagellate biology and ecology. Prog. Phycol. Res., 2, 147-188
13 Jin, H.J., G.M. Seo, Y.C. Cho, E.K. Hwang, C.H. Sohn and Y.K. Hong. 1997. Gelling agents for tissue culture of the seaweed Hizikia fusiformis. J. Appl. Phycol., 9, 489-493
14 Fletcher, R.L. 1991. Marine macroalgae as bioassay test organisms. In: Ectoxicology and the Marine Environment. Abel P.D. and V. Axiak eds., Ellis Horwood Ltd., New York, pp. 111-131
15 Gonzales, R.A. and J.M. Widholm. 1985. Selection of plant cells for desirable characteristics: Inhibitor resistance. In: Plant Cell Culture: A Practical Approach. Dixon, R.A. ed., IRL Press, Washington D.C., pp. 67-78
16 Hardisson, A, I. Frias and A. de Bonis. 1998. Mercury in algae of the Canary Islands littoral. Environ. International, 24, 945-950   DOI   ScienceOn