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Intraspecific competition in Fucus serratus and F. evanescens (Phaeophyceae: Fucales) germlings: effects of settlement density, nutrient concentration, and temperature

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Abstract

Survival and growth of early post-settlement stages are critical for the development of seaweed populations. Fucoid germlings commonly settle in dense monospecific aggregates, where intraspecific competition and environmental variables (e.g. nutrient concentration and temperature) may affect survival and growth. Using factorial experiments, we determined the effects of settlement density (~10, ~50 and ~250 germlings cm−2), nutrient enrichment (from ~10 to ~40 µM N and from ~0.5 to ~2.5 µM P), and temperature (7°C and 17°C) on Fucus serratus and F. evanescens germlings in laboratory cultures over 3 months. Settlement density, nutrient concentration and temperature interactively affected growth of germlings, and the magnitude of this interaction varied between the two species. This represents the first record of such factorial interactions in Fucus spp. germlings. Intraspecific competition, estimated as the relative reduction in germling growth and survival from low to high densities, increased with decreasing nutrient concentration and increasing temperature in both species. While temperature and nutrient concentration had little effect on germling size distributions, size inequality and skewness generally increased with germling density, indicating that a few large individuals gained dominance and suppressed many smaller ones at high density. Self-thinning increased with settlement density and depended on nutrient concentration and species at high density. At high density, self-thinning increased with decreasing nutrient levels in F. evanescens, but not in F. serratus. At low density, nutrient enrichment increased germling growth in F. evanescens, but not in F. serratus, whereas growth in both species was stimulated by nutrient enrichment at higher densities. These results suggest that germling growth and self-thinning are more sensitive to variation in nutrient concentration in F. evanescens than in F. serratus. The potential implications of our findings for the understanding of eutrophication-related abundance changes in both species in southern Norway are discussed.

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References

  • Andrew NL, Viejo RM (1998) Effects of wave exposure and intraspecific density on the growth and survivorship of Sargassum muticum (Sargassaceae: Phaeophyta). Eur J Phycol 33:251–258

    Article  Google Scholar 

  • Ang POJ, DeWreede RE (1992) Density-dependence in a population of Fucus distichus. Mar Ecol Prog Ser 90:169–181

    Google Scholar 

  • Arenas F, Fernández C (2000) Size structure and dynamics in a population of Sargassum muticum (Phaeophyceae). J Phycol 36:1012–1020

    Article  Google Scholar 

  • Arenas F, Viejo RM, Fernández C (2002) Density-dependent regulation in an invasive seaweed: responses at plant and modular levels. J Ecol 90:820–829

    Article  Google Scholar 

  • Arrontes J (2002) Mechanisms of range expansion in the intertidal brown alga Fucus serratus in northern Spain. Mar Biol 141:1059–1067

    Article  Google Scholar 

  • Bertness MD, Leonard GH, Levine JM, Schmidt PR, Ingraham AO (1999) Testing the relative contribution of positive and negative interactions in rocky intertidal communities. Ecology 80:2711–2726

    Google Scholar 

  • Bi H, Turvey ND (1997) A method of selecting data points for fitting the maximum biomass–density line for stands undergoing self-thinning. Aust J Ecol 22:356–359

    Google Scholar 

  • Bokn T, Lein TE (1978) Long-term changes in fucoid association of the inner Oslofjord, Norway. Norw J Bot 25:9–14

    Google Scholar 

  • Bokn TL, Murray S, Moy FE, Magnusson JB (1992) Changes in fucoid distribution and abundance in the inner Oslofjord, Norway: 1974–80 versus 1988–90. Acta Phytogeogr Suec 78:117–124

    Google Scholar 

  • Brawley SH, Johnson LE (1991) Survival of fucoid embryos in the intertidal zone depends upon developmental stage and microhabitat. J Phycol 27:179–186

    Google Scholar 

  • Carmer SG, Walker UM (1982) Baby Bear's dilemma: a statistical tale. Agron J 74:122–124

    Google Scholar 

  • Choi HG (2001) The effects of density on algal competition in culture and the field. PhD thesis, University of Liverpool, Liverpool

  • Creed JC (1995) Spatial dynamics of a Himanthalia elongata (Fucales, Phaeophyta) population. J Phycol 31:851–859

    Google Scholar 

  • Creed JC, Norton TA, Harding SP (1996a) The development of size structure in a young Fucus serratus population. Eur J Phycol 31:203–209

    Google Scholar 

  • Creed JC, Norton TA, Kain JM (1996b) Are neighbours harmful or helpful in Fucus vesiculosis populations? Mar Ecol Prog Ser 133:191–201

    Google Scholar 

  • Creed JC, Norton TA, Kain JM (1997) Intraspecific competition in Fucus serratus germlings: the interaction of light, nutrients and density. J Exp Mar Biol Ecol 212:211–223

    Google Scholar 

  • Creed JC, Kain JM, Norton TA (1998) An experimental evaluation of density and plant size in two large brown seaweeds. J Phycol 34:39–52

    Article  Google Scholar 

  • Crowley PH (1992) Resampling methods for computation-intensive data analysis in ecology and evolution. Annu Rev Ecol Syst 23:405–447

    Article  Google Scholar 

  • Dean TA, Thies K, Lagos SL (1989) Survival of juvenile giant kelp: the effects of demographic factors, competitors, and grazers. Ecology 70:483–495

    Google Scholar 

  • Dixon PM (2001) The bootstrap and the jackknife: describing the precision of ecological indices. In: Scheiner SM, Gurevitch J (eds) Design and analysis of ecological experiments. Oxford University Press, New York, pp 267–288

  • Grace JB (1995) On the measurement of plant competition intensity. Ecology 76:305–308

    Google Scholar 

  • Grenager B (1957) Algological observations from the polluted area of the Oslofjord. Nytt Mag Bot (Oslo) 5:41–60

    Google Scholar 

  • Grime JP (1977) Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. Am Nat 111:1169–1194

    Article  Google Scholar 

  • Howell DC (1992) Statistical methods for psychology. Duxbury, Belmont

  • Hruby T, Norton TA (1979) Algal colonization on rocky shores in the Firth of Clyde. J Ecol 67:65–77

    Google Scholar 

  • Hurlbert SH (1990) Pastor binocularis: now we have no excuse. Ecology 71:1222–1223

    Google Scholar 

  • Karez R (2003) Do monospecific stands of three Fucus species (Phaeophyta) comply with the 'self-thinning rule'? Eur J Phycol 38:171–180

    Google Scholar 

  • Kendrick GA (1994) Effects of propagule settlement density and adult canopy on survival of recruits of Sargassum spp. (Sargassaceae: Phaeophyta). Mar Ecol Prog Ser 103:129–140

    Google Scholar 

  • Kokko H, Mackenzie A, Reynolds JD, Lindstrom J, Sutherland WJ (1999) Measures of inequality are not equal. Am Nat 154:358–382

    Article  PubMed  Google Scholar 

  • Kristiansen S, Paasche E (1982) Nitrogen nutrition of the phytoplankton in the Oslofjord. Estuar Coast Shelf Sci 14:237–249

    Google Scholar 

  • Lonsdale WM (1990) The self-thinning rule: dead or alive? Ecology 71:1373–1388

    Google Scholar 

  • Lotze HK, Worm B, Sommer U (2001) Strong bottom-up and top-down control of early life stages of macroalgae. Limnol Oceanogr 46:749–757

    Google Scholar 

  • Markham JH, Chanway CP (1996) Measuring plant neighbour effects. Funct Ecol 10:548–549

    Google Scholar 

  • Markham JW, Hagmeier E (1982) Observations on the effects of germanium dioxide on the growth of macroalgae and diatoms. Phycologia 21:125–130

    CAS  Google Scholar 

  • Mead R (1991) The design of experiments. Statistical principles for practical applications. Cambridge University Press, Cambridge

  • Morris CE (1999) Density-dependent mortality induced by low nutrient status of the substrate. Ann Bot (Lond) 84:95–107

    Google Scholar 

  • Morris CE (2002) Self-thinning lines differ with fertility level. Ecol Res 17:17–28

    Article  Google Scholar 

  • Morris CE (2003) How does fertility of the substrate affect intraspecific competition? Evidence and synthesis from self-thinning. Ecol Res 18:287–305

    Article  Google Scholar 

  • Morris CE, Myerscough PJ (1985) Nutrient level effects on thinning and non-thinning crowding effects in even aged population of subterranean clover. Aust J Ecol 10:469–479

    Google Scholar 

  • Osawa A, Sugita S (1989) The self-thinning rule: another intepretation of Weller's results. Ecology 70:279–283

    Google Scholar 

  • Paine RT (1990) Benthic macroalgal competition: complications and consequences. J Phycol 26:12–17

    Google Scholar 

  • Quatrano RS (1980) Gamete release, fertilization, and embryogenesis in the Fucales. In: Gantt E (ed) Handbook of phycological methods. Developmental and cytological methods. Cambridge University Press, Cambridge, pp 59–68

  • Reed DC (1990) An experimental evaluation of density dependence in a subtidal algal population. Ecology 71:2286–2296

    Google Scholar 

  • Rueness J (1998) Alger i farger. Almater, Oslo

  • Schmitt HJ, Eccleston J, Ehrhardt DW (1987) Dominance and suppression, size-dependent growth and self-thinning in a natural Impatiens capensis population. J Ecol 75:651–665

    Google Scholar 

  • Schmitt J, Ehrhardt EW, Cheo M (1986) Light-dependent dominance and suppression in experimental radish populations. Ecology 67:1502–1507

    Google Scholar 

  • Silvertown JW, Charlesworth D (2001) Introduction to plant population biology. Blackwell, Oxford

  • Sokal RR, Rohlf FJ (1995) Biometry: the principles and practice of statistics in biological research. Freeman, New York

  • Soto D, Hurlbert SH (1991) Long-term experiments on calanoid–cyclopoid interactions. Ecol Monogr 61:245–265

    Google Scholar 

  • Steen H (2003) Intraspecific competition in Sargassum muticum (Phaeophyceae) germlings under various density, nutrient and temperature regimes. Bot Mar 46:36–43

    Google Scholar 

  • Steen H, Rueness J (2004) Comparison of survival and growth in germlings of six fucoid species (Fucales, Phaeophyceae) at two different temperature and nutrient levels. Sarsia (in press)

  • Turner MD, Rabinowitz D (1983) Factors affecting frequency distributions of plant mass: the absence of dominance and suppression in competing monocultures of Festuca paradoxa. Ecology 64:469–475

    Google Scholar 

  • Vadas RL Sr, Johnson S, Norton TA (1992) Recruitment and mortality of early post-settlement stages of benthic algae. Br Phycol J 27:331–351

    Google Scholar 

  • Weiner J (1985) Size hierarchies in experimental population of annual plants. Ecology 66:743–752

    Google Scholar 

  • Weiner J, Thomas SC (1986) Size variability and competition in plant monocultures. Oikos 47:211–222

    Google Scholar 

  • Weller DE (1987) A reevaluation of the −3/2 power rule of plant self-thinning. Ecol Monogr 57:23–43

    Google Scholar 

  • Weller DE (1989) The interspecific size–density relationship among crowded plant stands and its implications for the −3/2 power rule of self-thinning. Am Nat 133:20–41

    Article  Google Scholar 

  • Westoby M (1984) The self-thinning rule. Adv Ecol Res 14:167–225

    Google Scholar 

  • Worm B, Lotze HK, Sommer U (2001) Algal propagule banks modify competition, consumer and resource control on Baltic rocky shores. Oecologia 128:281–293

    Article  Google Scholar 

  • Yoda K, Kira T, Ogawa H, Hozumi K (1963) Self-thinning in overcrowded pure stands under cultivated and natural conditions. Intraspecific competition among higher plants. XI. J Biol Osaka City Univ 14:107–129

    Google Scholar 

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Acknowledgements

We thank the staff at the Norwegian Institute for Water Research (NIVA), Marine Research Station at Solbergstrand, for supplying seawater and nutrients. Thanks to Prof. J. Rueness, Dr. S. Fredriksen, Dr. T. Andersen, and Dr. L. J. Naustvoll, for sharing their knowledge and making helpful comments on earlier versions of the manuscript. Finally, we thank Dr. S. Blank, for providing valuable technical assistance with the resampling software, and two anonymous referees, for reviewing and improving the quality of this paper. This study complied with environmental laws of Norway.

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Correspondence to H. Steen.

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Communicated by L. Hagerman, Helsingør

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Steen, H., Scrosati, R. Intraspecific competition in Fucus serratus and F. evanescens (Phaeophyceae: Fucales) germlings: effects of settlement density, nutrient concentration, and temperature. Marine Biology 144, 61–70 (2004). https://doi.org/10.1007/s00227-003-1175-8

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