Skip to main content
Log in

Comparisons among species ofAlexandrium (Dinophyceae) grown in nitrogen- or phosphorus-limiting batch culture

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Three species of the dinoflagellate genusAlexandrium (Halim)-two strains of toxic.A. minutum, one each of nontoxicA. tamarense andA. affini-were grown in batch culture in either a low-nitrogen or a low-phosphate medium. Maximum carbon-specific growth rates forA. tamarense were lower (at <0.25 d-1) than for the other strains, which all exceeded 0.38 d-1. C-quotas (C content per cell) during exponential growth were similar for all strains (∼2.5 ng C cell-1), with cells becoming smaller during the N-limiting stationary phase, but enlarging during prolonged P-deprivation. Values of δ13C during the exponential phase were low (-25to-30), with most cells during the light phase swimming at the surface when nutrient-replete and migrating to the bottom of the flasks when nutrient-deplete with δ13C rising to around-15. Biomass could not be estimated reliably from pigmentation, but could be estimated from biovolume (r>0.95), although this was complicated in cultures ofA. minutum by the presence of particles comprized of thecal plates of a similar size to intact cells. Alkaline phosphatase activity was not a reliable indicator a P-status. The most toxic strain tested (A. minutum AL1V) contained the highest concentrations of free amino acids, of arginine (a precursor of paralytic shellfish toxins) and of proline, and also had the lowest C:N mass ratio (at 4.3).A. affini contained the lowest concentrations of arginine, andA. tamarense the highest exponential phase C:N (7.8). For all strains, the mole ratio of intracellular glutamine: glutamate (Gln: Glu, which was abnormally high compared to other algae) could only be used to indicate the presence or absence of N-stress rather than the degree of stress. Additions of ammonium and phosphate resulted in increases in Gln: Glu within 20 min in N-stressed cells and also enhanced toxin content inA. minutum (mainly gonyautoxin) 4 over a 24 h period.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Adachi M, Sako Y, Ishida Y (1993) Application of monoclonal antibodies to field samples ofAlexandrium species. Jap Soc Scient Fish 59: 1171–1175

    Google Scholar 

  • Anderson DM, Kulis DM, Sullivan JJ, Lee C (1990) Dynamics and physiology of saxtitoxin production by the dinoflagellatesAlexandrium spp. Mar Biol 104: 511–524

    Google Scholar 

  • Balech E (1988) Los dinoflagelados del Atlantico sudoccidental. Publnes esp Inst españ Oceanogr, Madrid 1: p 310

  • Bolch CJ, Blackburn SI, Cannon JA, Hallegraeff GM (1991) The resting cyst of the red-tide dinoflagellateAlexandrium minutum (Dinophyceae). Phycologia 30: 215–219

    Google Scholar 

  • Cannon JA (1993) Germination of the toxic dinoflagellateAlexandrium minutum from sediments in the Port River, South Australia. In: Smayda TJ, Shimizu Y (eds) Toxic Phytoplankton blooms in the sea. Elsevier, Amsterdam, pp 103–107

    Google Scholar 

  • Dixon GK, Syrett PJ (1988) The growth of dinoflagellates in laboratory cultures. New Phytol 109: 297–302

    Google Scholar 

  • Flores HE, Protacio CM, Signs MW (1989) Primary and secondary metabolism of polyamines in plants. Recent Adv Phytochem 23: 329–393

    Google Scholar 

  • Flynn K, Flynn KJ (1996) An automated HPLC method for the rapid analysis of paralytic shellfish toxins from dinoflagellates and bacteria using precolumn oxidation at low temperature. J exp mar Biol Ecol (In press)

  • Flynn K Flynn KJ, Jones KJ (1993) Intracellular amino acids in dinoflagellates; effects of diural changes in light and of N-supply. Mar Ecol Prog Ser 100: 245–252

    Google Scholar 

  • Flynn K, Franco JM, Fernandez P, Reguera B, Zapata M, Wood G, Flynn KJ (1994a) Changes in toxin content, biomass and pigments of the dinoflagellateAlexandrium minutum during nitrogen refeeding and growth into nitrogen or phosphorus stress. Mar Ecol Prog Ser 111: 99–109

    Google Scholar 

  • Flynn KJ (1990) The determination of nitrogen status in microalgae. Mar Ecol Prog Ser 61: 297–307

    Google Scholar 

  • Flynn KJ, Flynn K (1992) Non-protein amino acids in microalgae: consequences for the estimation of the glutamine/glutamate ratio. Mar Ecol Prog Ser 89: 73–79

    Google Scholar 

  • Flynn KJ, Jones KJ, Raine R Richard J, Flynn K (1994b) Use of intracellular amino acid analysis as an indicator of the physiological status of natural dinoflagellate populations. Mar Ecol Prog Ser 103: 175–186

    Google Scholar 

  • Franks PJS, Anderson DM (1992) Alongshore transport of a toxic phytoplankton bloom in a buoyancy current:Alexandrium tamarense in the Gulf of Maine. Mar Biol 112: 153–164

    Google Scholar 

  • Glibert PM, Dennett MR, Goldman JC (1985) Inorganic carbon uptake by phytoplankton in Vineyard Sound, Massachusetts. II. Comparative primary productivity and nutritional status of winter and summer assemblages. J exp mar Biol Ecol 86: 101–118

    Google Scholar 

  • Hallegraeff GM, Bolch CJ, Blackburn SI, Oshima Y (1991) Species of the toxigenic dinoflagellate genusAlexandrium in southeastern Australian waters. Botanica mar 34: 575–587

    Google Scholar 

  • Heath MR, Richardson K, Kioerboe T (1990) Optical assessment of phytoplankton nutrient depletion. J Plankton Res 12: 381–396

    Google Scholar 

  • Johnston AM, Raven JA (1992) Effect of aeration rates on growth rates and natural abundance13C/12C ratio ofPhaeodactylum tricornutum. Mar Ecol Prog Ser 87: 295–300

    Google Scholar 

  • Keller MD, Guillard RRL (1985) Factors significant to marine dinoflagellate culture. In: Anderson DM, White AW, Baden DG (eds) Toxic dinoflagellates. Elsevier, New York, pp 113–116

    Google Scholar 

  • Kuenzler EJ, Perras JP (1965) Phosphatases of marine algae. Biol Bull mar biol Lab, Woods Hole 128: 271–284

    Google Scholar 

  • Lirdwitayaprasit T, Nishio S, Montani S, Okaichi T (1990) The biochemical processes during cyst formation inAlexandrium catanella. In: Granelli E, Sundström B, Edler L, Anderson DM (eds) Toxic marine phytoplankton. Elsevier, New York, pp 294–297

    Google Scholar 

  • Montagnes DJS, Berges JA, Harrison PJ, Taylor FJR (1994) Estimating carbon, nitrogen, protein, and chlorophylla from volume in marine phytoplankton. Limnol Oceanogr 39: 1044–1060

    Google Scholar 

  • Raven JA (1991) Implications of inorganic carbon utilization: ecology, evolution and geochemistry. Can J Bot 69: 908–924

    Google Scholar 

  • Scholin CA, Anderson DM (1994) Identification of group-specific and strain-specific genetic markers for globally distributedAlexandrium (Dinophyceae). I. RFLP analysis of SSU ribosomal-RNA genes. J Phycol 30: 744–754

    Google Scholar 

  • Shimizu Y, Gupta S, Pradad AVK (1990) Biosynthesis of dinoflagellate toxins. In: Granelli E, Sundström B, Edler L, Anderson DM (eds) Toxic marine phytoplankton Elsevier, New York, pp 62–71

    Google Scholar 

  • Steidinger KA, Moestrup Ø (1990) The taxonomy ofGonyaulax, Pyrodinium, Alexandrium, Gessnerium, Protogonyaulax andGoniodoma. In: Granelli E, Sundström B, Edler L, Anderson DM (eds) Toxic marine phytoplankton. Elsevier, New York, pp 522–523

    Google Scholar 

  • Strickland JDH, Parsons TR (1972) A practical handbook of seawater analysis. 2nd edn. Bull Fish Res Bd Can 167: 1–310

    Google Scholar 

  • Vrieling EG, Peperzak L, Gieskes WWC, Veenhuis M (1994) Detection of the ichthyotoxic dinoflagellateGyrodinium (cf.)aureolum and morphologically relatedGymnodinium species using monoclonal antibodies: a specific immunological tool. Mar Ecol Prog Ser 103: 165–174

    Google Scholar 

  • White AW Nassif J, Shumway SE, Whittaker DK (1993) Recent occurrence of paralytic shellfish toxins in offshore shellfish in the northern United States. In: Smayda TJ, Shimizu Y (eds) Toxic phytoplankton blooms in the sea. Elsevier, Amsterdam, pp 435–440

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J. P. Thorpe, Port Erin

Rights and permissions

Reprints and permissions

About this article

Cite this article

Flynn, K., Jones, K.J. & Flynn, K.J. Comparisons among species ofAlexandrium (Dinophyceae) grown in nitrogen- or phosphorus-limiting batch culture. Mar. Biol. 126, 9–18 (1996). https://doi.org/10.1007/BF00571372

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00571372

Keywords

Navigation