Ecological Archives E092-182-A1

Kyle F. Edwards, Christopher A. Klausmeier, and Elena Litchman. 2011. Evidence for a three-way trade-off between nitrogen and phosphorus competitive abilities and cell size in phytoplankton. Ecology 92:2085–2095.

Appendix A. List of species in the data set and references for trait data.

TABLE A1. Freshwater species in the data set. Measured values are indicated by ‘X’.

Taxon Species
VN
max
KN
QN
min
VP
max
KP
QP
min
Volume Reference
Cyanobacteria Anabaena cylindrica X X X X X X X 18
Cyanobacteria Anabaena flos-aquae       X X   X 62,83
Cyanobacteria Anabaena planktonica       X X X X 92
Cyanobacteria Anabaena sp.       X       63
Cyanobacteria Anabaena variabilis             X 42
Cyanobacteria Anacystis nidulans     X       X 90
Chlorophyte Ankistrodesmus convolutus       X X     66
Cyanobacteria Aphanizomenon flos-aquae       X X X X 92
Diatom Asterionella formosa X X X X X X X 34,35,92,97
Diatom Asterionella ralfsii             X 30
Chlorophyte Carteria sp.   X         X 39
Chlorophyte Chlamydomonas acidophila       X X X X 93
Chlorophyte Chlamydomonas reinhardtii           X X 37,42
Chlorophyte Chlamydomonas sp.       X X   X 66
Chlorophyte Chlorella sp.       X   X X 38
Chlorophyte Chlorella vulgaris   X   X X X X 39,50,66,72,74,90
Chlorophyte Chlorococcum hypnosporum   X         X 39
Chlorophyte Coelastrum microporum X X X X X X X 18
Desmid Cosmarium abbreviatum       X X X X 94
Desmid Cosmarium subcostatum       X X X X 44
Cryptomonad Cryptomonas           X X 37
Diatom Cyclotella meneghiniana       X X X   89,97
Cyanobacteria Cylindrospermopsis raciborskii       X X X X 47
Diatom Diatoma elongatum       X X X X 52
Chlorophyte Dictyosphaerium pulchellum X X X X X X X 18
Chrysophyte Dinobryon cylindricum       X X   X 55
Chrysophyte Dinobryon sociale       X X   X 55
Chlorophyte Euglena gracilis       X X X X 13
Diatom Fragilaria bidens X X X X X X X 18
Diatom Fragilaria capucina           X X 37
Diatom Fragilaria crotonensis X X X X X X X 34,35,92
Cyanobacteria Gloeocapsa alpicola X X         X 33
Chlorophyte Golenkiniopsis sp.   X         X 39
Dinoflagellate Gymnodinium bogoriense       X X   X 56
Diatom Hantzschia amphyoxis   X         X 39
Chlorophyte Koliella sp.   X         X 39
Cyanobacteria Microcystis aeruginosa X X X X X X X 2,33,42,67
Cyanobacteria Microcystis sp.       X       18
Xanthophyte Monodus subterraneus       X X X X 72
Chlorophyte Monoraphidium griffithii       X X X X 72
Chlorophyte Monoraphidium minutum X X X X X X X 18
Chlorophyte Monoraphidium sp.   X         X 39
Diatom Navicula pelliculosa X X   X     X 39,62,102
Diatom Nitzschia acicularis           X X 37
Diatom Nitzschia linearis           X X 37
Diatom Nitzschia palea           X X 37
Diatom Nitzschia sp.1   X         X 39
Diatom Nitzschia sp.2   X         X 39
Chlorophyte Oocystis pusilla           X X 37
Chlorophyte Pediastrum boryanum X X X X X X X 18
Dinoflagellate Peridinium cinctum   X     X   X 91
Cyanobacteria Planktothrix agardhii       X X X X 21,33
Cyanobacteria Prochlorothrix hollandica       X X X X 21
Cyanobacteria Pseudanabaena catenata               42
Chlorophyte Scenedesmus crassus X X X X X X X 18
Chlorophyte Scenedesmus obliquus   X X     X X 39,82
Chlorophyte Scenedesmus quadricauda X X X X X X X 18,37,38,42,62,103
Chlorophyte Scenedesmus sp. X X X X X X X 79
Chlorophyte Selenastrum capricornutum   X   X X X X 39,42,72
Chlorophyte Sphaerocystis schroeteri           X X 37
Desmid Staurastrum chaetoceros       X X X X 94
Desmid Staurastrum luetkemuellerii       X X X   67
Desmid Staurastrum paradoxum       X X X X 44
Desmid Staurastrum pingue       X X X X 94
Cyanobacteria Synechococcus linearis X   X X   X X 43
Cyanobacteria Synechocystis sp.       X X X X 72
Diatom Synedra acus       X X X X 92
Diatom Synedra radians           X X 37
Diatom Synedra rumpens           X X 37
Diatom Synedra ulna       X X X X 92
Diatom Thalassiosira gravida               17
Chlorophyte Volvox aureus       X X   X 88
Chlorophyte Volvox globator       X X   X 88

TABLE A2. Marine species in the dataset. Measured values indicated by ‘X’.

Taxon Species
VN
max
KN
QN
min
VP
max
KP
QP
min
Volume Reference
Dinoflagellate Alexandrium catenella       X X X X 49,68
Dinoflagellate Alexandrium minutum X X X X X X X 11,59
Dinoflagellate Alexandrium tamarense X X X X X X X 19,91
Dinoflagellate Amphidinium carterae       X X   X 20,91
Cyanobacteria Aphanothece stagnina     X       X 6
Diatom Asterionella glacialis X X X     X X 17,25
Pelagophyte Aureoumbra lagunensis           X X 57
Diatom Biddulphia aurita X X         X 99
Diatom Chaetoceros affinis           X X 48
Diatom Chaetoceros curvisetus             X 77
Diatom Chaetoceros debilis     X       X 90
Diatom Chaetoceros gracilis   X X       X 25,90
Diatom Chaetoceros lorenzianus X X         X 75
Diatom Chaetoceros simplex     X       X 31,90
Diatom Chaetoceros sp.               77
Raphidophyte Chattonella antiqua X X X X X X X 61
Raphidophyte Chattonella ovata     X     X X 106
Diatom Coscinodiscus lineatus X X         X 25
Diatom Coscinodiscus wailesii X X X X X X X 25,65
Diatom Cyclotella cryptica       X X X X 1
Diatom Ditylum brightwellii X X         X 23,25
Chlorophyte Dunaliella tertiolecta X X X X X X X 4,6,31,36,58,
77,90,91,105
Coccolithophore Emiliania huxleyi X X X X X X X 25,26,69,84,85
Diatom Eucampia zodiacus X X X X X X X 64
Diatom Fragilaria pinnata   X     X   X 9,91
Coccolithophore Gephyrocapsa oceanica             X 84
Dinoflagellate Gonyaulax polyedra   X         X 91
Dinoflagellate Gymnodinium breve       X   X X 100
Dinoflagellate Gymnodinium catenatum X X X X X X X 109
Dinoflagellate Gymnodinium sanguineum X X         X 71,91
Dinoflagellate Heterocapsa circularisquama     X     X X 107
Dinoflagellate Heterocapsa triquetra       X X X X 11,91
Raphidophyte Heterosigma akashiwo X X X X X X X 45,98,104
Raphidophyte Heterosigma carterae     X       X 26
Haptophyte Isochrysis galbana   X X       X 5
Diatom Leptocylindrus danicus   X         X 25
Chlorophyte Mantoniella sp.             X 51,53
Chlorophyte Micromonas pusilla X X         X 15
Chlorophyte Nannochloris sp. X X         X 71
Diatom Nitzschia closterium       X X X X 1,8,90
Diatom Nitzschiella longissima X X         X 87
Dinoflagellate Peridinium sp.       X X     91
Haptophyte Phaeocystis pouchetii       X X   X 101
Diatom Phaeodactylum tricornutum X X X X   X X 31,54,76,78,96,105
Chlorophyte Platymonas sp.             X 51,53
Dinoflagellate Prorocentrum donghaiense       X X X X 68
Dinoflagellate Prorocentrum micans X X         X 75
Dinoflagellate Prorocentrum minimum X X   X X   X 10,71,91
Dinoflagellate Protogonyaulax tamarensis       X X   X 10
Diatom Pseudo-nitzschia australis   X         X 16
Diatom Pseudo-nitzschia pungens X X X X X X X 12
Dinoflagellate Pyrocystis fusiformis X X X       X 3,90
Dinoflagellate Pyrocystis lunula     X       X 90
Dinoflagellate Pyrocystis noctiluca X X X X X X X 3,86,90
Diatom Rhizosolenia robusta X X         X 71
Diatom Rhizosolenia stolterfothii   X         X 25
Diatom Skeletonema costatum X X X X X X X 17,25,40,41,48,
68,87,87,90,91,95
                   
Dinoflagellate Symbiodinium microadriaticum       X X     20
Cyanobacteria Synechococcus       X X X X 28,46
Chlorophyte Tetraselmis subcordiformis       X X X X 14
Diatom Thalassiosira oceanica   X     X   X 25,91
Diatom Thalassiosira pseudonana X X X X X X X 6,7,8,9,19,24,29,32,
51,70,73,90,91,105,110
Diatom Thalassiosira rotula           X X 48
Diatom Thalassiosira weissflogii       X X X X 29,31,90
Cyanobacteria Trichodesmium       X X X X 27,60

LITERATURE CITED

1. Admiraal, W., and D. Werner. 1983. Utilization of limiting concentrations of ortho-phosphate and production of extracellular organic phosphates in cultutres of marine diatoms. Journal of Plankton Research 5:495–513.

2. Baldia, S. F., A. D. Evangelista, E. V. Aralar, and A. E. Santiago. 2007. Nitrogen and phosphorus utilization in the cyanobacterium Microcystis aeruginosa isolated from Laguna de Bay, Philippines. Journal of Applied Phycology 19:607–613.

3. Bhovichitra, M., and E. Swift. 1977. Light and dark uptake of nitrate and ammonium by large oceanic dinoflagellates - Pyrocystis noctiluca, Pyrocystis fusiformis, and Dissodinium lunula. Limnology and Oceanography 22:73–83.

4. Bienfang, P. K. 1975. Steady-state analysis of nitrate-ammonium assimilation by phytoplankton. Limnology and Oceanography 20:402–411.

5. Caperon, J. 1968. Population growth response of Isochrysis galbana to nitrate variation at limiting concentrations. Ecology 49:866–872.

6. Caperon, J., and J. Meyer. 1972. Nitrogen-limited growth of marine phytoplankton. II. Uptake kinetics in nutrient limited growth of phytoplankton. Deep-Sea Research 19:619–632.

8. Carpenter, E. J. 1970. Phosphorus requirements of two planktonic diatoms in steady state culture. Journal of Phycology 6:28–30.

9. Carpenter, E. J., and R. R. L. Guillard. 1971. Intraspecific differences in nitrate half-saturation constants for three species of marine phytoplankton. Ecology 52:183–185.

10. Cembella, A. D., N. J. Antia, and P. J. Harrison. 1984. The utilization of inorganic and organic phorphorus compounds as nutrients by eukaryotics microalgae: a multidisciplinary perspective. Part 2. Crc Critical Reviews in Microbiology 11:13–81.

11. Chapelle, A., C. Labry, M. Sourisseau, C. Lebreton, A. Youenou, and M. P. Crassous. 2010. Alexandrium minutum growth controlled by phosphorus: An applied model. Journal of Marine Systems 83:181–191.

12. Cheng, Z., and Z. Jingzhong. 1997. Nutrient uptake kinetics and growth under nutrient limitation of Pseduo-nitzschia. Oceanologia et limnologia sinica 28:599–603.

13. Chisholm, S. W., and R. G. Stross. 1976. Phosphate uptake kinetics in Euglena gracilis grown in light-dark cycles. 2. Phased PO4-limited cultures. Journal of Phycology 12:217–222.

14. Nan, C., and S. Dong. 2004. Comparative studies on phosphorus uptake and growth kinetics of the microalga Tetraselmis subcordiformis and the macroalga Ulva pertusa. Journal of Ocean University of China 3:56–59.

15. Cochlan, W. P., and P. J. Harrison. 1991. Kinetics of nitrogen (nitrate, ammonium and urea) uptake by the picoflagellate Micromonas pusilla (Prasinophyceae). Journal of Experimental Marine Biology and Ecology 153:129–141.

16. Cochlan, W. P., J. Herndon, and R. M. Kudela. 2008. Inorganic and organic nitrogen uptake by the toxigenic diatom Pseudo-nitzschia australis (Bacillariophyceae). Harmful Algae 8:111–118.

17. Conway, H. L., and P. J. Harrison. 1977. Marine diatoms grown in chemostats under silicate or ammonium limitation. 4. Transienct response of Chaetoceros debilis, Skeletonema costatum, and Thalassiosira gravida to a single addition of limiting nutrient. Marine Biology 43:33–43.

18. Dauta, A. 1982. Conditions de developpement du phytoplancton: etude comparative du comportement de huit especes en cultures. II. Role des nutriments: assimilation et stockage. Annales De Limnologie-International Journal of Limnology 19:73–86.

19. Davidson, K., and W. S. C. Gurney. 1999. An investigation of non-steady-state algal growth. II. Mathematical modelling of co-nutrient-limited algal growth. Journal of Plankton Research 21:839–858.

20. Deane, E. M., and R. W. Obrien. 1981. Uptake of phosphate by symbiotic and free-living dinoflagellates. Archives of Microbiology 128:307–310.

21. Ducobu, H., J. Huisman, R. R. Jonker, and L. R. Mur. 1998. Competition between a prochlorophyte and a cyanobacterium under various phosphorus regimes: Comparison with the Droop model. Journal of Phycology 34:467–476.

22. Elrifi, I. R., and D. H. Turpin. 1985. Steady-state luxury consumption and the concept of optimum nutrient ratios: A study with phosphate and nitrate limited Selenastrum minutum (Chlorophyta). Journal of Phycology 21:592–602.

23. Eppley, R. W., and Coatsworth J. l. 1968. Uptake of nitrate and nitrite by Ditylum brightwellii: kinetics and mechanisms. Journal of Phycology 4:151–156.

24. Eppley, R. W., and E. H. Renger. 1974. Nitrogen assimilation of an oceanic diatom in nitrogen-limited continuous culture. Journal of Phycology 10:15–23.

25. Eppley, R. W., J. N. Rogers, and J. J. Mccarthy. 1969. Half-saturation constants for uptake of nitrate and ammonium by marine phytoplankton. Limnology and Oceanography 14:912–920.

26. Flynn, K. J., S. Page, G. Wood, and C. R. Hipkin. 1999. Variations in the maximum transport rates for ammonium and nitrate in the prymnesiophyte Emiliania huxleyi and the raphidophyte Heterosigma carterae. Journal of Plankton Research 21:355–371.

27. Fu, F. X., Y. H. Zhang, P. R. F. Bell, and D. A. Hutchins. 2005. Phosphate uptake and growth kinetics of Trichodesmium (Cyanobacteria) isolates from the North Atlantic Ocean and the Great Barrier Reef, Australia. Journal of Phycology 41:62–73.

28. Fu, F. X., Y. H. Zhang, Y. Y. Feng, and D. A. Hutchins. 2006. Phosphate and ATP uptake and growth kinetics in axenic cultures of the cyanobacterium Synechococcus CCMP 1334. European Journal of Phycology 41:15–28.

29. Fuhs, G. W., S. D. Demmerle, E. Canelli, and M. Chen. 1972. Characterization of phosphorus-limited algae. In G. E. Likens [ed.], Nutrients and eutrophication. Allen Press Inc.

30. Gensemer, R. W., R. E. H. Smith, and H. C. Duthie. 1993. Comparative effects of pH and aluminum on slica-limited growth and nutrient uptake in Asterionella ralfsii var. americana (Bacillariophyceae). Journal of Phycology 29:36–44.

31. Goldman, J. C., and P. M. Glibert. 1982. Comparative rapid ammonium uptake by four species of marine phytoplankton. Limnology and Oceanography 27:814–827.

32. Goldman, J. C., and J. J. Mccarthy. 1979. Steady state growth and ammonium uptake of a fast-growing marine diatom. Limnology and Oceanography 23:695–703.

34. Gotham, I. J., and G. Y. Rhee. 1981. Comparative kinetic studies of nitrate-limited growth and nitrate uptake in phytoplankton continuous culture. Journal of Phycology 17:309–314.

35. ---. 1981. Comparative kinetic studies of phosphate-limited growth and phosphate uptake in phytoplankton continuous culture. Journal of Phycology 17:257–265.

36. Graziano, L. M., J. Laroche, and R. J. Geider. 1996. Physiological responses to phosphorus limitation in batch and steady-state cultures of Dunaliella tertiolecta (Chlorophyta): A unique stress protein as an indicator of phosphate deficiency. Journal of Phycology 32:825–838.

37. Grover, J. P. 1989. Phorphorus-dependent growth kinetics of 11 species of freshwater algae. Limnology and Oceanography 34:341–348.

38. ---. 1991. Non-steady-state dynamics of algal population growth: Experiments with two chlorophytes. Journal of Phycology 27:70–79.

39. Halterman, S. G., and D. W. Toetz. 1984. Kinetics of nitrate uptake by freshwater algae. Hydrobiologia 114:209–214.

40. Harrison, P. J., H. L. Conway, and R. C. Dugdale. 1976. Marine diatoms grown in chemostats under silicate of ammonium limitation. 1. Cellular chemical composition and steady-state growth kinetics of skeletonema costatum. Marine Biology 35:177–186.

41. Harrison, P. J., H. L. Conway, R. W. Holmes, and C. O. Davis. 1977. Marine diatoms grown  in chemostats under silicate or ammonium limitation. 3. Cellular chemical composition and morphology of Chaetoceros debilis, Skeletonema costatum, and Thalassiosira gravida. Marine Biology 43:19–31.

42. Healey, F. P. 1977. Ammonium and urea uptake by some freshwater algae. Canadian Journal of Botany-Revue Canadienne De Botanique 55:61–69.

43. ---. 1985. Interacting effects of light and nutrient limitation on the growth rate of Synechococcus linearis (Cyanophyceae). Journal of Phycology 21:134–146.

44. Healey, F. P., and L. L. Hendzel. 1988. Competition for phosphorus between desmids. Journal of Phycology 24:287–292.

45. Hosaka, M. 1992. Growth characteristics of a strain of Heterosigma akashiwo (Hada) Hada isolated from Tokyo Bay, Japan. Bulletin of Plankton Society of Japan 39:49–58.

46. Ikeya, T., K. Ohki, M. Takahashi, and Y. Fujita. 1997. Study on phosphate uptake of the marine cyanophyte Synechococcus sp NIBB 1071 in relation to oligotrophic environments in the open ocean. Marine Biology 129:195–202.

47. Istvanovics, V., H. M. Shafik, M. Presing, and S. Juhos. 2000. Growth and phosphate uptake kinetics of the cyanobacterium, Cylindrospermopsis raciborskii (Cyanophyceae) in throughflow cultures. Freshwater Biology 43:257–275.

48. Jahnke, J., H. J. Rick, and L. Aletsee. 1986. On the light and temperature-dependence of the minimum and maximum phosphorus contents in cells of the marine plankton diatom Thalassiosira rotula. Journal of Plankton Research 8:549–555.

49. Jauzein, C., C. Labry, A. Youenou, J. Quere, D. Delmas, and Y. Collos. 2010. Growth and phosphorus uptake by the toxic dinoflagellate Alexandrium catenella (Dinophyceae) in response to phosphate limitation. Journal of Phycology 46:926–936.

50. Jeanfils, J., M. F. Canisius, and N. Burlion. 1993. Effect of high nitrate concentrations on growth and nitrate uptake by free-living and immobilized Chlorella vulgaris cells. Journal of Applied Phycology 5:369–374.

51. Kanda, J., and A. Hattori. 1988. Ammonium uptake and synthesis of cellular nitrogenous macromolecules in phytoplankton. Limnology and Oceanography 33:1568–1579.

52. Kilham, S. S., C. L. Kott, and D. Tilman. 1977. Phosphate and silicate kinetics for the Lake Michigan diatom Diatom elongatum. Journal of Great Lakes Research 3.

53. Koike, I., D. G. Redalje, J. W. Ammerman, and O. Holmhansen. 1983. High-affinity uptake of an ammonium analog by two marine microflagellates from the oligotrophic Pacific. Marine Biology 74:161–168.

54. Kuenzler, E. J., and B. H. Ketchum. 1962. Rate of phosphorus uptake by Phaeodactylum tricornutum. Biological Bulletin 123:134–145.

55. Lehman, J. T. 1976. Ecological and nutritional studies on dinobryon Ehrenb.: seasonal periodicity and phosphate toxicity problem. Limnology and Oceanography 21:646–658.

56. Lieberman, O. S., M. Shilo, and J. Vanrijn. 1994. The physiological ecology of a freshwater dinoflagellate bloom population: vertical migration, nitrogen limitation, and nutrient uptake kinetics. Journal of Phycology 30:964–971.

57. Liu, H. B., E. A. Laws, T. A. Villareal, and E. J. Buskey. 2001. Nutrient-limited growth of Aureoumbra lagunensis (Pelagophyceae), with implications for its capability to outgrow other phytoplankton species in phosphate-limited environments. Journal of Phycology 37:500–508.

58. Lomas, M. W., and P. M. Glibert. 2000. Comparisons of nitrate uptake, storage, and reduction in marine diatoms and flagellates. Journal of Phycology 36:903–913.

59. Maguer, J. F., S. L'helguen, C. Madec, C. Labry, and P. Le Corre. 2007. Nitrogen uptake and assimilation kinetics in Alexandrium minutum (Dynophyceae): Effect of N-limited growth rate on nitrate and ammonium interactions. Journal of Phycology 43:295–303.

60. Mulholland, M. R., and D. G. Capone. 1999. Nitrogen fixation, uptake and metabolism in natural and cultured populations of Trichodesmium spp. Marine Ecology-Progress Series 188:33–49.

61. Nakamura, Y., and M. M. Watanabe. 1983. Nitrate and phosphate uptake kinetics of Chattonella antiqua grown in light/dark cycles. Journal of the Oceanographical Society of Japan 29:167–170.

62. Nalewajko, C., and D. R. S. Lean. 1978. Phosphorus kinetics: algal growth relationships in batch cultures. Internationale Vereiningung fur Theoretische und Angewandte Limnologie, Mittelungen 21:184–192.

63. Nalewajko, C., and T. P. Murphy. 2001. Effects of temperature, and availability of nitrogen and phosphorus on the abundance of Anabaena and Microcystis in Lake Biwa, Japan: An experimental approach. Limnology 2:45–48.

64. Nishikawa, T., K. Tarutani, and T. Yamamoto. 2009. Nitrate and phosphate uptake kinetics of the harmful diatom Eucampia zodiacus Ehrenberg, a causative organism in the bleaching of aquacultured Porphyra thalli. Harmful Algae 8:513–517.

65. ---. 2010. Nitrate and phosphate uptake kinetics of the harmful diatom Coscinodiscus wailesii, a causative organism in the bleaching of aquacultured Porphyra thalli. Harmful Algae 9:563–567.

66. Oh, H. M., and G. Y. Rhee. 1991. A comparative study of microalgae isolated from flooded rice paddies: light-limited growth, C-fixation, growth efficiency and relative-N and relative-P requirement. Journal of Applied Phycology 3:211–220.

67. Olsen, Y. 1989. Evaluation of competitive ability of Staurastrum leutkemuellerii (Chlorophyceae) and Microcystis aeruginosa (Cyanophyceae) under P limitation. Journal of Phycology 25:486–499.

67. Olsen, Y., O. Vadstein, T. Andersen, and A. Jensen. 1989. Competition between Staurastrum luetkemuellerii (Chlorophyceae) and Microcystis aeruginosa (Cyanophyceae) under varying modes of phosphate supply. Journal of Phycology 25:499–508.

68. Ou, L. J., D. Wang, B. Q. Huang, H. S. Hong, Y. Z. Qi, and S. H. Lu. 2008. Comparative study of phosphorus strategies of three typical harmful algae in Chinese coastal waters. Journal of Plankton Research 30:1007–1017.

69. Page, S., C. R. Hipkin, and K. J. Flynn. 1999. Interactions between nitrate and ammonium in Emiliania huxleyi. Journal of Experimental Marine Biology and Ecology 236:307–319.

70. Parslow, J. S., P. J. Harrison, and P. A. Thompson. 1984. Saturated uptake kinetics: transient response of the marine diatom Thalassiosira pseudonana to ammonium, nitrate, silicate or phosphate starvation. Marine Biology 83:51–59.

71. Pasciak, W. J., and J. Gavis. 1974. Transport limitation of nutrient uptake in phytoplankton. Limnology and Oceanography 19:881–898.

72. Passarge, J., S. Hol, M. Escher, and J. Huisman. 2006. Competition for nutrients and light: Stable coexistence, alternative stable states, or competitive exclusion? Ecological Monographs 76:57–72.

73. Perry, M. J. 1976. Phosphate utilization by an oceanic diatom in phosphorus-limited chemostat culture and in oligotrophic waters of the central North Pacific. Limnology and Oceanography 21:88–107.

74. Pickett, J. M. 1975. Growth of Chlorella in a nitrate-limited chemostat. Plant Physiology 55:223–225.

75. Qi, Y. Z., and C. J. Zhu. 1994. A comparative study of nitrate uptake kinetics by two red tide causative algae. Asian Marine Biology 11:103–106.

76. Raimbault, P., G. Slawyk, and V. Gentilhomme. 1990. Direct measurements of nanomolar nitrate uptake by the marine diatom Phaedactylum tricornutum (Bohlin): implications for studies of oligotrophic ecosystems. Hydrobiologia 207:311–318.

77. Reay, D. S., D. B. Nedwell, J. Priddle, and J. C. Ellis-Evans. 1999. Temperature dependence of inorganic nitrogen uptake: Reduced affinity for nitrate at suboptimal temperatures in both algae and bacteria. Applied and Environmental Microbiology 65:2577–2584.

78. Rees, T. A. V., C. M. Grant, H. E. Harmens, and R. B. Taylor. 1998. Measuring rates of ammonium assimilation in marine algae: Use of the protonophore carbonyl cyanide m-chlorophenylhydrazone to distinguish between uptake and assimilation. Journal of Phycology 34:264–272.

79. Rhee, G. Y. 1973. Continuous culture study of phosphate uptake, growth rate and polyphosphate in Scenedesmus sp. Journal of Phycology 9:495–506.

80. ---. 1974. Phosphate uptake under nitrate limitation by Scenedesmus sp. and its ecological implications. Journal of Phycology 10:470–475.

81. ---. 1978. Effects of N:P atomic ratios and nitrate limitation on algal growth, cell composition, and nitrate uptake. Limnology and Oceanography 23:10–25.

82. Rhee, G. Y., and I. J. Gotham. 1981. The effect of environmental factors on phytoplankton growth: temperature and the interactions of temperature with nutrient limitation. Limnology and Oceanography 26:635–648.

83. Rhee, G. Y., and T. C. Lederman. 1983. Effects of nitrogen sources on P-limited growth of Anabaena flos-aquae. Journal of Phycology 19:179–185.

84. Rhodes, L. L., B. M. Peake, A. L. Mackenzie, and S. Marwick. 1995. Coccolithophores Gephyrocapsa oceanica and Emiliania huxleyi (Prymnesiophyceae = Haptophyceae) in New Zealand coastal waters: characteristics of blooms and growth in laboratory culture. New Zealand Journal of Marine and Freshwater Research 29:345–357.

85. Riegman, R., W. Stolte, A. A. M. Noordeloos, and D. Slezak. 2000. Nutrient uptake, and alkaline phosphate (EC 3 : 1 : 3 : 1) activity of Emiliania huxleyi (Prymnesiophyceae) during growth under N and P limitation in continuous cultures. Journal of Phycology 36:87–96.

86. Rivkin, R. B., and E. Swift. 1982. Phosphate uptake by the oceanic dinoflagellate Pyrocystis noctiluca. Journal of Phycology 18:113–120.

87. Romeo, A. J., and N. S. Fisher. 1982. Intraspecific comparisons of nitrate uptake in three marine diatoms. Journal of Phycology 18:220–225.

88. Senft, W. H., R. A. Hunchberger, and K. E. Roberts. 1981. Temperture-dependence of growth and phosphorus uptake in two species of Volvox (Volvolcales, Chlorophyta). Journal of Phycology 17:323–329.

89. Shafik, H. M., S. Herodek, M. Presing, L. Voros, and K. V. Balogh. 1997. Growth of Cyclotella meneghiniana Kutz. II. Growth and cell composition under different growth rates with different limiting nutrient. Annales De Limnologie-International Journal of Limnology 33:223–233.

90. Shuter, B. J. 1978. Size dependence of phorphorus and nitrogen subsistence quotas in unicellular microorganisms. Limnology and Oceanography 23:1248–1255.

91. Smayda, T. J. 1997. Harmful algal blooms: Their ecophysiology and general relevance to phytoplankton blooms in the sea. Limnology and Oceanography 42:1137–1153.

92. Smith, R. E. H., and J. Kalff. 1982. Size-dependent phosphorus uptake kinetics and cell quota in phytoplankton. Journal of Phycology 18:275–284.

93. Spijkerman, E. 2007. Phosphorus acquisition by Chlamydomonas acidophila under autotrophic and osmo-mixotrophic growth conditions. Journal of Experimental Botany 58:4195–4202.

94. Spijkerman, E., and P. F. M. Coesel. 1996. Phosphorus uptake and growth kinetics of two planktonic desmid species. European Journal of Phycology 31:53–60.

95. Tarutani, K., and T. Yamamoto. 1994. Phosphate uptake and growth kinetics of Skeletonema costatum isolated from Hiroshima Bay. Journal of the Faculty of Applied Biological Science Hiroshima University 33:59–64.

96. Terry, K. L., J. Hirata, and E. A. Laws. 1985. Light-limited, nitrogen-limited, and phosphorus-limited growth of Phaeodactylum tricornutum (Bohlin) strain TFX-1: chemical composition, carbon partitioning, and the diel periodicity of physiological processes. Journal of Experimental Marine Biology and Ecology 86:85–100.

97. Tilman, D., and S. S. Kilham. 1976. Phosphate and silicate growth and uptake kinetics of the diatoms Asterionella formosa and Cyclotella meneghiniana in batch and semi-continuous culture. Journal of Phycology 12:375–383.

98. Tomas, C. R. 1979. Olisthodiscus luteus (Chrysophyceae). 3. Uptake and utilization of nitrogen and phosphorus. Journal of Phycology 15:5–12.

99. Underhill, P. A. 1977. Nitrate uptake kinetics and clonal variability in neritic diatom Biddulphia aurita. Journal of Phycology 13:170–176.

100. Vargo, G. A., and D. Howardshamblott. 1990. Phosphorus dynamics in Ptychodiscus brevis: cell phosphorus, uptake and growth requirements. Toxic Marine Phytoplankton: 324–329.

101. Veldhuis, M. J. W., F. Colijn, and W. Admiraal. 1991. Phosphate utilization in Phaeocystis pouchetii (Haptophyceae). Marine Ecology-Pubblicazioni Della Stazione Zoologica Di Napoli I 12:53–62.

102. Wallen, D. G., and L. D. Cartier. 1975. Molybdenum dependence, nitrate uptake and photosynthesis of freshwater plankton algae. Journal of Phycology 11:345–349.

103. Watanabe, T., and T. Miyazaki. 1996. Maximum ammonium uptake rates of Scenedesmus quadricauda (Chlorophyta) and Microcystis novacekii (Cyanobacteria) grown under nitrogen limitation and implications for competition. Journal of Phycology 32:243–249.

104. Watanabe, M., K. Kohata, and M. Kunugi. 1987. P-31 nuclear magnetic resonance study of intracellular phosphate pools and polyphosphate metabolism in Heterosigma akashiwo (Hada) (Raphidophyceae). Journal of Phycology 23:54–62.

105. Wynne, D., and G. Y. Rhee. 1986. Effects of light intensity and quality on the relative N-requirement and P-requirement (the optimum N:P ratio) of marine planktonic algae. Journal of Plankton Research 8:91–103.

106. Yamaguchi, H., S. Sakamoto, and M. Yamaguchi. 2008. Nutrition and growth kinetics in nitrogen- and phosphorus-limited cultures of the novel red tide flagellate Chattonella ovata (Raphidophyceae). Harmful Algae 7:26–32.

107. Yamaguchi, M., S. Itakura, and T. Uchida. 2001. Nutrition and growth kinetics in nitrogen- or phosphorus-limited cultures of the 'novel red tide' dinoflagellate Heterocapsa circularisquama (Dinophyceae). Phycologia 40:313–318.

108. Yamamoto, T., S. J. Oh, and Y. Kataoka. 2004. Growth and uptake kinetics for nitrate, ammonium and phosphate by the toxic dinoflagellate Gymnodinium catenatum isolated from Hiroshima Bay, Japan. Fisheries Science 70:108–115.

109. Yamamoto, T., and K. Tarutani. 1999. Growth and phosphate uptake kinetics of the toxic dinoflagellate Alexandrium tamarense from Hiroshima Bay in the Seto Inland Sea, Japan. Phycological Research 47:27–32.

110. Zehr, J. P., P. G. Falkowski, J. Fowler, and D. G. Capone. 1988. Coupling between ammonium uptake and incorporation in a marine diatom: experiments with the short-lived radioisotope N-13. Limnology and Oceanography 33:518–527.


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