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研究生:黃郁琪
研究生(外文):Yu-Chi Huang
論文名稱:柱孢藻之相剋物質研究
論文名稱(外文):The study of allelochemicals from Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju
指導教授:吳俊宗
指導教授(外文):Jiunn-Tzong Wu
學位類別:碩士
校院名稱:國立臺灣大學
系所名稱:生態學與演化生物學研究所
學門:生命科學學門
學類:生態學類
論文種類:學術論文
論文出版年:2008
畢業學年度:96
語文別:中文
論文頁數:64
中文關鍵詞:柱胞藻相剋物質脂肪酸鉀離子滲漏
外文關鍵詞:Cylindrospermopsis raciborskiiallelochemicalsfatty acidK+-leakage
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柱孢藻 (Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju) 為一種絲狀的淡水藍綠菌。源自於熱帶、亞熱帶地區,但近幾十年來快速入侵至溫帶地區並能大量滋長。柱孢藻在一些優養化水庫中有大量生長的情況,其優勢生長之情形,豐度有時可達98%以上,因而嚴重影響水庫的水質。過去之研究並發現,柱孢藻能快速及大量生長的物理化學環境因子,與其他藻類相較並無特別之處,因此懷疑其能大量滋長係與相剋物質有關,故本研究擬加以驗證。
本實驗之材料為純化自金門水庫的柱孢藻,經大量培養後收集其質量。先用80%酒精萃取以得到粗萃取物,再經液相分層方法,分別收集有機萃取物及水溶性萃取物。測試各萃取物分別對Chlorella vulgaris、Anabaena sp.及Microcystis aeruginosa等的生長抑制作用,發現均有不同程度的抑制作用,證明萃取物質中含有相剋物質。有機萃取物經氣相層析儀 (GC/MS) 分析其成分,發現含有數種脂肪酸:Palmitic acid (PA, 16:0)、Palmitoleic acid (PTA, 16:1)、Linoleic acid (LA, 18:2) 及a-Linolenic acid (ALA, 18:3)等。經個別測試脂肪酸,發現都會對三株測試藻種造成不同程度的生長抑制效果。水溶性萃取物部分再以C18管柱及不同濃度之甲醇淋洗,其具有生長抑制效果的部分分別在0、75、90及100%甲醇分樣中。但以氣相層析儀 (GC-MS) 分析其成分時,發現活性物質除含PA外,另外還有其他未知的高極性物質。
當分別添加PA、PTA及ALA至C. vulgaris及M. aeruginosa藻液中,後二者都會造成藻細胞明顯的鉀離子滲漏,而PA則無明顯的影響。C. vulgaris的滲漏作用約在1小時後就會達到穩定,但在M. aeruginosa則需要較久的時間,顯示對脂肪酸較具耐抗性。使用穿透式電子顯微鏡觀察ALA對M. aeruginosa細胞微細構造的影響,發現1小時之後細胞膜會皺縮,使得細胞膜與細胞壁分離而形成空隙,空隙並隨著時間增加而空隙加大。
綜合以上結果,證明柱孢藻可能會以產生脂肪酸作為相剋物質,而成為水域之優勢物種。所產生之不飽和脂肪酸擬以造成其他藻細胞的破壞及鉀離子滲漏而致毒,飽和脂肪酸則毒性較弱。除脂肪酸外,相剋物質另疑尚有其他高極性物質,此有待進一步研究。
Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju is a filamentous freshwater cyanobacterium. It has been widely distributed in the tropical and subtropical regions and widespread to temperate climate regions during last few decades. It often formed algal bloom or predominated in phytoplankton assemblages in certain water reservoirs and thus affected seriously the water quality. The conditions for its massive growth are not very different from those of common cyanobacteria or chlorophytes in the eutrophic environment. Thus, it is speculated that the outgrowth of C. raciborskii might be related to an allelopathic effect. The present study is done to verify this.
The strain of C. raciborskii used for this study was isolated from the water reservoir of Kinmen. After mass-culture in the laboratory, the cells were harvested and extracted with 80% ethanol solution. The extract was separated by liquid-liquid partitioning to get organic and water-soluble extracts. The growth inhibition test with Chlorella vulgaris, Anabaena sp. and Microcystis aeruginosa showed that positive inhibitory effect was observed in both the organic and water-soluble extracts. Analyses with GC-MS and bioassay indicated that active compounds in organic extract were palmitic acid (PA, 16:0), palmitoleic acid (PTA, 16:1), linoleic acid (LA, 18:2), and a-linolenic acid (ALA, 18:3). For the water-soluble extract, a partial purification with a C18 liquid-solid-partition column was done. Positive inhibitory effect was detected for the eluted fractions of 0%, 75%, 90% and 100% methanol. Nevertheless, analysis with GC-MS showed that all of these fractions contained a common fatty acid, palmitic acid. In addition to this, there was an highly polar, unknown active compound which needed to be further studied.
The treatment of C. vulgaris or M. aeruginosa cells with both the PTA and ALA would cause a remarkable K+-leakage from cells to extracellular medium, while no significant effect was observed by treating with PA. In response to the treatment with fatty acids, M. aeruginosa displayed higher tolerance than C. vulgaris, in the time course as well as in the magnitude of K+-leakage. Observation under transmission electron microscope showed that ALA would result in ultrastructural changes of M. aeruginosa, causing a shrinkage in intracellular membranes to give rise to spaces between cell wall and membranes. The resultant space increased in size and number over time after ALA treatment.
In conclusion, this study verified that C. raciborskii might produce fatty acids as the allelochemicals to inhibit the growth of other algae in the aquatic environment. The fatty acids, particularly of polyunsaturated species, would exert cytotoxic effects on the target cells, causing ultrastructural changes and damages in cell membranes. As a result, leakage of potassium from the intracellular to extracellular medium as a symptom of cell damages was observed
誌謝 I
中文摘要 II
英文摘要 IV
縮寫表 V
一、前言 1
二、材料與方法 7
2.1柱孢藻來源 7
2.2柱孢藻的培養 7
2.2.1培養條件 7
2.2.2柱孢藻的細胞材料 7
2.3柱孢藻相剋物質之分離及鑑定 7
2.3.1柱孢藻之胞內粗萃取物製備 7
2.3.2柱孢藻之有機萃取液成分鑑定 8
2.3.3柱孢藻之水溶性萃取液成分分離及鑑定 8
2.3.4氣相層析/質譜儀分析條件 8
2.4測試藻株對柱孢藻粗萃取毒性物質的敏感度 8
2.4.1測試方法 8
2.4.2測試藻株種類 9
2.4.3葉綠素a濃度測量方法 9
2.4.4生長速率計算方法 9
2.4.5生長抑制率之計算 10
2.4.6半抑制濃度 10
2.5脂肪酸的定量 10
2.5.1柱孢藻粗萃取物有機層之脂肪酸抽取 10
2.5.2脂肪酸衍生反應 10
2.5.3脂肪酸標準品衍生物之製備 11
2.5.4脂肪酸HPLC定性定量分析 11
2.6測試藻株對柱孢藻所產生之脂肪酸的敏感度測試 11
2.7脂肪酸對藻細胞之鉀離子滲漏的影響 11
2.7.1測試藻種 11
2.7.2鉀離子濃度測量方法 12
2.7.3細胞內外之初始鉀離子濃度測定 12
2.7.4有毒脂肪酸對藻細胞鉀離子滲漏的測試 12
2.8以電子顯微鏡觀察微囊藻細胞膜受脂肪酸之影響 12
2.9金門陽明湖中藻類種類、數量及水質之調查 13
2.9.1湖中浮游藻類採樣 13
2.9.2定性片的製作及計數 13
2.9.3定量片的製作及計數 14
2.9.4水樣分析 14
三、結果 15
3.1柱孢藻乙醇萃取物之毒性測試 15
3.1.1有機萃取物之生長抑制結果 15
3.1.2水溶性萃取物之生長抑制結果 15
3.1.3水溶性萃取物各分樣之生長抑制活性 15
3.2柱孢藻相剋物質之定性和定量分析 16
3.2.1 GC/MS分析 16
3.2.2 GC/MS分析水溶性萃取物中內含物質 16
3.2.3脂肪酸之HPLC定性定量分析 17
3.3游離脂肪酸對藻類生長之抑制 17
3.3.1飽和脂肪酸之生長抑制 17
3.3.2不飽和脂肪酸之生長抑制結果 17
3.4柱孢藻相剋物質對其他藻細胞之鉀離子滲漏效應 18
3.5電子顯微鏡觀察結果 19
3.6陽明湖中藻類種類、數量 20
3.7陽明湖之水質調查 20
四、討論 21
五、結論 28
參考文獻 29
表 36
圖 44
張雅雯,2005,柱孢藻在金門水庫水庫形成優勢之原因探討,國立臺灣大學植物科學研究所碩士論文,113頁
Berger, C., N. Ba, M. Gugger, M. Bouvy, F. Rusconi, A. Couté, M. Troussellier, and C. Bernard. 2006. Seasonal dynamics and toxicity of Cylindrospermopsis raciborskii in Lake Guiers (Senegal, West Africa). FEMS Microbiology Ecology 57:355–366.
Berland, B. R., D. J. Bonin, and A. L. Cornu. 1979. The antibacterial substances of the marine alga Stichochrysis immobilis(Chrysophyta) Journal of Phycology 8:383-392.
Bouaϊcha, N., and A.-B. Nasri. 2004. First report of cyanobacterium Cylindrospermopsis raciborskii from Algerian freshwaters. Environmental Toxicology 19:541-543.
Bouvy, M., D. Falcão, M. Marinho, M. Pagano, and A. Moura. 2000. Occurrence of Cylindrospermopsis (Cyanobacteria) in 39 Brazilian tropical reservoirs during the 1998 drought. Aquatic Microbial Ecology 23:13-27.
Branco, C. W. C., and P. A. C. Senna. 1994. Factors influencing the development of Cylindrospermopsis raciborskii and Microcystis aeruginosa in the Paranoa Reservoir, Brasilia, Brazil. Algological studies 75:85-96.
Briand, J.-F., C. Leboulanger, J.-F. Humbert, C. Bernard, and P. Dufour. 2004. Cylindrospermopsis raciborskii (cyanobacteria) invasion at mid-latitudes: selection, wide physiological tolerance, or global warming? Journal of Phycology 40:231 - 238.
Briand, J. F., C. Robillotb, C. Quiblier-Llobérasc, J. F. Humbertd, A. Cout!ea, and C. Bernarda. 2002. Environmental context of Cylindrospermopsis raciborskii (Cyanobacteria) blooms in a shallow pond in France. Water Research 36:3183–3192.
Chellappa, N. T., and M. A. M. Costa. 2003. Dominant and co-existing species of Cyanobacteria from a Eutrophicated reservoir of Rio Grande do Norte State, Brazil. Acta Oecologica 24:S3-S10.
Chiang, I.-Z., W.-Y. Huang, and J.-T. Wu. 2004. Allelochemicals of Botryococcus braunii (chlorophyceae). Journal of Phycology 40:474-480.
Chonudomkul, D., W. Yongmanitchai, G. Theeragool, M. Kawachi, F. Kasai, K. Kaya, and M. M. Watanabe. 2004. Morphology, genetic diversity, temperature tolerance and toxicity of Cylindrospermopsis raciborskii (Nostocales, Cyanobacteria) strains from Thailand and Japan. FEMS Microbiology Ecology 48:345–355.
De Cano, M. M. S., M. C. Z. De Mul, G. Z. De Caire, and D. R. De Halperin. 1990. Inhibition of Candida albicans and Staphylococcus aureus byphenolic compounds from the terrestrial cyanobacterium Nostoc muscorum. Journal of Applied Phycology 2:79-91.
Duff, D. C. B., D. L. Bruce, and N. J. Antia. 1966. The antibacterial activity of marine planktonic algae. Canadian journal of microbiology 12:877-884.
Fabbro, L. D., and L. J. Duivenvoorden. 1996. Profile of a bloom of the cyanobacterium Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju in the Fitzroy River in tropical Centrol Queensland. Freshwater Research 47:685-694.
Fastner, J., R. Heinze, A. R. Humpage, U. Mischke, G. K. Eaglesham, and I. Chorus. 2003. Cylindrospermopsin occurrence in two German lakes and preliminary assessment of toxicity and toxin production of Cylindrospermopsis raciborskii (Cyanobacteria) isolates. Toxicon 42:313-321.
FerrãoFilho, A. d. S., S. M. da Costa, M. G. L. Ribeiro, and S. M. F. O. Azevedo. 2007. Effects of a Saxitoxin-Producer Strain of Cylindrospermopsis raciborskii (Cyanobacteria) on the Swimming Movements of Cladocerans. Environmental Toxicology 23:161-168.
Flores, E., and C. P. Wolk. 1986. Production, by filamentous, nitrogen- fixing cyanobacteria, of a bacteriocin and of other antibiotics that kill related strains. Archives of Microbiology 145:215-219.
Froscio, S. M., A. R. Humpage, P. C. Burcham, and I. R. Falconer. 2003. Cylindrospermopsin-Induced Protein Synthesis Inhibition and Its Dissociation from Acute Toxicity in Mouse Hepatocytes. Environmental Toxicology 18:243 - 251.
Gantar, M., J. P. Berry, S. Thomas, M. Wang, R. Perez, and K. S. Rein. 2008. Allelopathic activity among Cyanobacteria and microalgae isolated from Florida freshwater habitats. FEMS Microbiology Ecology 64:55-64.
Gleason, F. K., and J. L. Paulson. 1984. Site of action of the natural algicide, cyanobacterin, in the blue-green alga, Synechococcus sp. Archives of Microbiology 138:273-277.
Hamilton, P. B., L. M. Ley, D. Stuart, and F. R. Pick. 2003. The occurrence of the cyanobacterium Cylindrospermopsis raciborskii in Constance Lake: an exotic cyanoprokaryote new to Canada. Phycologia:17–25.
Hawkins, P. R., N. R. Chandrasena, G. J. Jones, A. R. Humpage, and I. R. Falconer. 1997. Isolation and toxicity of Cylindrospermopsis raciborskii from an ornamental lake. Toxicon 35:341-346.
Hiroyuki, H., and Y. Takaaki. 1977. Illustrations of the Japanese fresh-water algae. Uchida-Rokakuho, Tokyo.
Humpage, A. R., M. Fenech, P. Thomas, and I. R. Falconer. 2000. Micronucleus induction and chromosome loss in transformed human white cells indicate clastogenic and aneugenic action of the cyanobacterial toxin, cylindrospermopsin. Mutation Research 472:155–161.
Istvánovics, V., L. Somlyódy, and A. Clement. 2002. Cyanobacteria-mediated internal eutrophication in shallow Lake Balaton after load reduction. Water Research 36:3314-3322.
Jüttner, F., and J. T. Wu. 2000. Evidence of allelochemical activity in subtropical cyanobacterial biofilms of Taiwan. Archiv fur Hydrobiologie 147:505-517.
Jandl, G., H.-R. Schulten, and P. Leinweber. 2002. Quantification of long-chain fatty acids in dissolved organic matter and soils. Journal of Plant Nutrition and Soil Science 165:133-139.
Kinnear, S. H. W., A. L. D. Fabbro, and A. L. J. Duivenvoorden. 2008. Variable Growth Responses of Water Thyme (Hydrilla verticillata) to Whole-Cell Extracts of Cylindrospermopsis raciborskii. Archives of environmental contamination and toxicology 54:187-194.
Kiss, T., Á. Vehovszky, L. Hiripi, A. Kovács, and L. Vörös. 2002. Membrane effects of toxins isolated from a cyanobacterium, Cylindrospermopsis raciborskii, on identified molluscan neurones. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 131:167-176.
Komárek, J., and B. Fott. 1983. Das phytoplankton des Süβwassers. 7 edition. Teil(1.Hälfte). E. Schweizerbart''sche, Verlagsbuchhandlung, Stuttgart.
Krebs, C. J. 1985. Ecology : The Experimental Analysis of Distribution and Abundance. 3 edition. Harper & Row Inc., New YorK.
Lagosa, N. s., H. Onoderab, P. Z. Antonio, D. o. Andrinoloa, S. M. F. Q. Azevedod, and Y. Oshima. 1999. The first evidence of paralytic shellfish toxins in the freshwater cyanobacterium Cylindrospermopsis raciborskii, isolated from Brazil. Toxicon 37:1359-1373.
Leflaive, J., and L. Ten-Hage. 2007. Algal and cyanobacterial secondary metabolites in freshwaters: a comparison of allelopathic compounds and toxins. Freshwater Biology 52:199-214.
Legrand, C., K. Rengefors, G. O. Fistarol, and E. Graneli. 2003. Allelopathy in phytoplankton - biochemical, ecological and evolutionary aspects. Phycologia 42:406-419.
Li, R., W. W. Carmichael, S. Brittain, G. K. Eaglesham, G. R. Shaw, Y. Liu, and M. M. Watanabe. 2001. First report of the cyanotoxins cylindrospermopsin and deoxycylindrospermopsin from Raphidiopsis curvata (cyanobacteria). Toxicon 37:1121-1126.
Loya, S., V. Reshef, E. Mizrachi, C. Silberstein, Y. Rachamim, S. Carmeli, and A. Hizi. 1998. The Inhibition of the Reverse Transcriptase of HIV-1 by the Natural Sulfoglycolipids from Cyanobacteria: Contribution of Different Moieties to Their High Potency. Journal of natural products 61:891-895.
Marshall, J.-A., T. Ross, S. Pyecroft, and G. Hallegraeff. 2005. Superoxide production by marine microalgae. Marine Biology 147:541-549.
McCracken, M. D., R. E. Middaugh, and R. S. Middaugh. 1980. A chemical characterization of an algal inhibitor obtained from chlamydomonas. Hydrobiologia 70:271-276.
Metcalf, J. S., A. Barakate, and G. A. Codd. 2004. Inhibition of plant protein synthesis by the cyanobacterial hepatotoxin, cylindrospermopsin. Pages 125-129.
Metcalf, J. S., J. Lindsay, K. A. Beattie, S. Birmingham, M. L. Saker, A. K. Törökné, and G. A. Codd. 2002. Toxicity of cylindrospermopsin to the brine shrimp Artemia salina: comparisons with protein synthesis inhibitors and microcystins. Toxicon 40:1115-1120.
Mohamed, Z. A. 2007. First reportof toxic Cylindrospermopsis raciborskiiand Raphidiopsismediterranea(Cyanoprokaryota) in Egyptian freshwaters. FEMS Microbiology Ecolology 59 749-761.
Moisander, P. H., E. McClinton, and H. W. Paerl. 2002. Salinity Effects on Growth, Photosynthetic Parameters, and Nitrogenase Activity in Estuarine Planktonic Cyanobacteria. Microbial Ecology 43:432-442.
Moore, D., G. B. McGregor, and G. Shaw. 2004. Morphological changes during akinete germination in Cylindrospermopsis raciborskii (Nostocales, cyanobacteria). Journal of Phycology 40:1098-1105.
Moore, D., M. O''Donohue, C. Garnett, C. Critchley, and G. Shaw. 2005. Factors affecting akinete differentiation in Cylindrospermopsis raciborskii (Nostocales, Cyanobacteria). Freshwater Biology 50:345-352.
Nakai, S., S. Yamada, and M. Hosomi. 2005. Anti-cyanobacterial fatty acids released from Myriophyllum spicatum. Hydrobiologia 543:71-78.
Neumann, C., P. Bain, and G. Shaw. 2007 Studies of the comparative in vitro toxicology of the cyanobacterial metabolite deoxycylindrospermopsin. J Toxicol Environ Health A 70:1679-1686.
Nogueira, I. C. G., A. Lobo-da-Cunha, and V. M. Vasconcelos. 2006. Effects of Cylindrospermopsis raciborskii and Aphanizomenon ovalisporum (cyanobacteria) ingestion on Daphnia magna midgut and associated diverticula epithelium. Aquatic Toxicology 80:194-203.
Norris, R. L. G., G. K. Eaglesham, G. Pierens, and G. R. Shaw. 1999. Deoxycylindrospermopsin, an analog of cylindrospermopsin from Cylindrospermopsis raciborskii Environmental Toxicology 14.
Ohta, S., Y. Shiomi, A. Kawashima, O. Aozasa, T. Nakao, T. Nagate, K. Kitamura, and H. Miyata. 1995. Antibiotic effect of linolenic acid from Chlorococcum strain HS-101 and Dunaliella primolecta on methicillin-resistant Staphylococcus aureus. Journal of Applied Phycology 7:121-127.
Ohtani, I., R. E. Moore, and M. T. C. Runnegar. 1992. Cylindrospermopsin: A Potent Hepatotoxin from the Blue-Green Alga Cylindrospermopsis raciborskii. Journal of the American Chemical Society 114: 7941-7942.
Padisak, J. 1997. Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju, an expanding, highly adaptative cyanobacterium: worldwilde distribution and review of its ecology. . Arch. Hydrobiol. Suppl. 107:563–593.
Papke, U., E. M. Gross, and W. Francke. 1997. Isolation, identification and determination of the absolute configuration of Fischerellin B. A new algicide from the freshwater cyanobacterium Fischerella muscicola (Thuret). Tetrahedron Letters 38:379-382.
Piccardi, R., A. Frosini, M. R. Tredici, and M. C. Margheri. 2000. Bioactivity in free-living and symbiotic cyanobacteria of the genus Nostoc. Journal of Applied Phycology 12:543-547.
Pomati, F., C. Rossetti, D. Calamari, and B. A. Neilan1. 2003. Effects of Saxitoxin (STX) and Veratridine on Bacterial NaP+ P- KP+ PFluxes: a Prokaryote-Based STX Bioassay. Applied and Environmrntal Microbiology 69:7371–7376.
Proctor, V. W. 1957. Some Controlling Factors in the Distribution of Haematococcus Pluvialis. Ecology 38:457-462.
Ramamurthy, V. D. 1970. Antibacterial activity of the marine blue-green algae Trichodesmium erythraeum in the gastro-intestinal tract of the sea gull Larus brumicephalus. Marine Biology 6:74-76.
Rezanka, T., and V. M. Dembitsky. 2006. Metabolites produced by cyanobacteria belonging to several species of the Family Nostocaceae Folia Microbiologica 51:159-182.
Rice, E. L. 1984. Allelopathy. Academic Press, New York.
Runnegar, M. T., S.-M. Kong, Y.-Z. Zhong, and S. C. Lu. 1995. Inhibition of reduced glutathione synthesis by cyanobacterial alkaloid cylindrospermopsin in cultured rat hepatocytes. Biochemical Pharmacology 49:219–225.
Runnegar, M. T., C. Xie, S. B. B., G. A. Wallace, S. M. Weinreb, and K. J. 2002. In vitro hepatotoxicity of the cyanobacterial alkaloid cylindrospermopsin and related synthetic analogues. Toxxicological sciences 67:81-87.
Saker, M. L., and G. K. Eaglesham. 1999. The accumulation of cylindrospermopsin from the cyanobacterium Cylindrospermopsis raciborskii in tissues of the Redclaw crayfish Cherax quadricarinatus. Toxicon 37: 1065-1077.
Saker, M. L., J. S. Metcalf, G. A. Codd, and V. M. Vasconcelos. 2004. Accumulation and depuration of the cyanobacterial toxin cylindrospermopsin in the freshwater mussel Anodonta cygnea. Toxicon 43:185-194.
Saker, M. L., B. A. Neilan, and D. J. Griffiths. 1999. Two morphological forms of Cylindrospermopsis raciborskii (cyanobacteria) isolated from solomon dam, palm island, queensland. Journal of Phycology 35:599-606.
Saker, M. L., I. C. G. Nogueira, V. M. Vasconcelos, B. A. Neilan, G. K. Eaglesham, and P. Pereira. 2003. First report and toxicological assessment of the cyanobacterium Cylindrospermopsis raciborskii from Portuguese freshwaters. Ecotoxicology and Environmental Safety 55:243-250.
Schembri, M. A., B. A. Neilan, and C. P. Saint. 2001. Identification of Genes Implicated in Toxin Production in the Cyanobacterium Cylindrospermopsis raciborskii. Environmental Toxicology 16:413-421.
Schlegel, I., N. Doan, N. de Chazal, and G. Smith. 1998. Antibiotic activity of new cyanobacterial isolates from Australia and Asia against green algae and cyanobacteria. Journal of Applied Phycology 10:471-479.
Scutt, J. E. 1964 Autoinhibitor production by Chlorella vulgaris. American journal of botany 51:581-584.
Scutt, J. E. A. p. b. C. v., M. D. Am. J. Bot . 51 : 581-584 .McCracken, R. E. Middaugh, and R. S. Middaugh. 1980. A chemical characterization of an algal inhibitor obtained from chlamydomonas. Hydrobiologia 70:271-276.
Sieburth, J. M. 1959. Acrylic acid, an ''antibiotic'' principle in Phaeocystis blooms in antiarctic waters. Science 132:676 - 677.
Smith, G., and N. Thanh Doan. 1999. Cyanobacterial metabolites with bioactivity against photosynthesis in cyanobacteria, algae and higher plants. Journal of Applied Phycology 11:337-344.
Srivastava, A., F. Jüttner, and R. J. Strasser. 1998. Action of the allelochemical, fischerellin A, on photosystem II. Biochimica et Biophysica Acta (BBA) - Bioenergetics 1364:326-336.
Suzuki, M., I. Wakana, T. Denboh, and M. Tatewaki. 1996. An allelopathic polyunsaturated fatty acid from red algae. Phytochemistry 43:63-65.
Takamo, K., S. Igarashi, and H. H. S. Mikami. 2003. Causation of reversal simultaneity for diatom biomass and density of Phormidium tenue during the warm season in eutrophic Lake Barato, Japan. Limnology 4:73-78.
Tsuchiya, H., T. Hayashi, M. Sato, M. Tatsumi, and N. Takagi. 1984. Simultaeous separation and sensutuve determination of free acids in blood plasma by high-performance liquid chromatography. Jounal of chromatography 309:43-52.
US Enviromental Protection Agency. 1992. In vitromdetermination of chlorophyll a and pheophytin a in marine and freshwater phytoplankton by fluorescence. Method 445.0. Cincinnati, Ohio.
Várkonyi, Z., O. Zsiros, T. Farkas, G. Garab, and Z. Gombos. 2000. The tolerance of cyanobacterium Cylindrospermopsis raciborskii to low temperature photo-inhibition affected by the induction of polyunsaturated fatty acid synthesis. Biochemical Society Transactions 28:892-894.
White, S. H., L. J. Duivenvoorden, L. D. Fabbro, and G. K. Eaglesham. 2006. Influence of intracellular toxin concentrations on cylindrospermopsin bioaccumulation in a freshwater gastropod (Melanoides tuberculata). Toxicon 47:497-509.
White, S. H., L. J. Duivenvoorden, L. D. Fabbro, and G. K. Eaglesham. 2007. Mortality and toxin bioaccumulation in Bufo marinus following exposure to Cylindrospermopsis raciborskii cell extracts and live cultures. Environmental Pollution 147:158-167.
Wood, S. A., and D. J. Stirling. 2003. First identification of the cylindrospermopsin-producing cyanobacterium Cylindrospermopsis raciborskii in New Zealand. New Zealand Journal of Marine and Freshwater Research 37:821-828.
Wu, J.-T., Y.-R. Chiang, W.-Y. Huang, and W.-N. Jane. 2006. Cytotoxic effects of free fatty acids on phytoplankton algae and cyanobacteria. Aquatic Toxicology 80:338-345.
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