Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Crop and Pasture Science Crop and Pasture Science Society
Plant sciences, sustainable farming systems and food quality
RESEARCH ARTICLE

Reproduction strategy of Chloris virgata under simulated atmospheric nitrogen deposition

Wang Changfu A and Wang Ying A B
+ Author Affiliations
- Author Affiliations

A Key Laboratory of Songliao Aquatic Environment, Ministry of Education, Jilin Jianzhu University, Changchun 130118, China.

B Corresponding author. Email: wangying19879@aliyun.com

Crop and Pasture Science 66(5) 516-521 https://doi.org/10.1071/CP14306
Submitted: 26 June 2014  Accepted: 11 December 2014   Published: 29 April 2015

Abstract

Atmospheric nitrogen (N) deposition is an important issue of global climate change and it will significantly affect plant growth and reproduction, resulting in damage to ecological systems. However, little attention has been given to the effects of this factor on plant reproductive strategies. We investigated how variation in atmospheric N deposition affects the reproductive strategy of Chloris virgata (feathertop Rhodes grass). We simulated atmospheric N deposition to evaluate the trade-off between seed size and seed number, as well as its effects on offspring vigour. We found significant negative correlations between seed size and seed number per spike in the control and 20.0 g N m–2 treatments, as well as between seed size and seed number per plant in the control treatment. Seed number and seed weight per spike behaved similarly and were significantly lower in the control and 20.0 g N m–2 treatments than in the other N supply treatments. Spike number and seed yield behaved similarly, and the greatest gains in these values occurred from 2.5 to 20.0 g N m–2. Seed size reached its maximum values at low and high N levels, whereas seed N concentrations increased with N level. Although the germination percentage remained stable under different N levels, the highest germination rate occurred in the control treatment. Our findings showed that simulated atmospheric N deposition affected the reproductive pattern and seed vigour of C. virgata.

Additional keywords: germination, reproduction, seed size, trade-off.


References

International Seed Testing Association (1985) International rules for testing seeds. Seed Science and Technology 13, 299–355.

Clark CM, Tilman D (2008) Loss of plant species after chronic low-level nitrogen deposition to prairie grasslands. Nature 451, 712–715.
Loss of plant species after chronic low-level nitrogen deposition to prairie grasslands.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhs1KnsL8%3D&md5=3f309689429ab285b070772b0cfbb4f0CAS | 18256670PubMed |

Donohue K, Schmitt J (1998) Maternal environmental effects in plants: adaptive plasticity? In ‘Maternal effects as adaptions’. (Eds TA Mousseau, CW Fox) pp. 137–158. (Oxford University Press: Oxford, UK)

Fenner M (1991) Effects of parent plant environment on seed size and chemical composition. Horticultural Reviews 13, 183–213.

Fortunel C, Violle C, Roumet C, Buatois B, Navas M, Garnier E (2009) Allocation strategies and seed traits are hardly affected by nitrogen supply in 18 species differing in successional status. Perspectives in Plant Ecology, Evolution and Systematics 11, 267–283.
Allocation strategies and seed traits are hardly affected by nitrogen supply in 18 species differing in successional status.Crossref | GoogleScholarGoogle Scholar |

Galloway LF (2001) Parental environmental effects on life history in the herbaceous plant Campanula Americana. Ecology 82, 2781–2789.
Parental environmental effects on life history in the herbaceous plant Campanula Americana.Crossref | GoogleScholarGoogle Scholar |

Galloway LF (2005) Maternal effects provide phenotypic adaptation to local environmental conditions. New Phytologist 166, 93–99.
Maternal effects provide phenotypic adaptation to local environmental conditions.Crossref | GoogleScholarGoogle Scholar | 15760354PubMed |

Galloway JN, Dentener FJ, Capone DG, Boyer EW, Howarth RW, Seitzinger SP, Asner GP, Cleveland CC, Green PA, Holland EA, Karl DM, Michaels A, Porter FJH, Townsend AR, Vǒrǒsmarty CJ (2004) Nitrogen cycles: Past, present, and future. Biogeochemistry 70, 153–226.
Nitrogen cycles: Past, present, and future.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXpsFShtw%3D%3D&md5=1c2ae68534fcf74d1ca60e3b79cb77a1CAS |

Gómez JM (2004) Bigger is not always better: conflicting selective pressures on seed size in Quercus ilex. Evolution 58, 71–80.
Bigger is not always better: conflicting selective pressures on seed size in Quercus ilex.Crossref | GoogleScholarGoogle Scholar | 15058720PubMed |

Hallett LM, Standish RJ, Hobbs RJ (2011) Seed mass and summer drought survival in a Mediterranean-climate ecosystem. Plant Ecology 212, 1479–1489.
Seed mass and summer drought survival in a Mediterranean-climate ecosystem.Crossref | GoogleScholarGoogle Scholar |

Hanley ME, Cordier PK, May O, Kelly CK (2007) Seed size and seedling growth: differential response of Australian and British Fabaceae to nutrient limitation. New Phytologist 174, 381–388.
Seed size and seedling growth: differential response of Australian and British Fabaceae to nutrient limitation.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2s7oslyrtQ%3D%3D&md5=b406e0b3e4ce68eb769e22d3744c963dCAS | 17388900PubMed |

Huxman TE, Charlet TN, Grant C, Smith SD (2001) The effects of parental CO2 and offspring nutrient environment on initial growth and photosynthesis in an annual grass. International Journal of Plant Sciences 162, 617–623.
The effects of parental CO2 and offspring nutrient environment on initial growth and photosynthesis in an annual grass.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXktFyktLw%3D&md5=a1d97bfd15365e1def7af84fe9ec17adCAS |

Jakobsson A, Eriksson O (2000) A comparative study of seed number, seed size, seedling size and recruitment in grassland plants. Oikos 88, 494–502.
A comparative study of seed number, seed size, seedling size and recruitment in grassland plants.Crossref | GoogleScholarGoogle Scholar |

Kidson R, Weatoby M (2000) Seed mass and seedling dimensions in relation to seedling establishment. Oecologia 125, 11–17.
Seed mass and seedling dimensions in relation to seedling establishment.Crossref | GoogleScholarGoogle Scholar |

Leishman MR (2001) Does the seed size/number trade-off model determine plant community structure? An assessment of the model mechanisms and their generality. Oikos 93, 294–302.
Does the seed size/number trade-off model determine plant community structure? An assessment of the model mechanisms and their generality.Crossref | GoogleScholarGoogle Scholar |

Leishman MR, Wright IJ, Moles AT, Westoby M (2000) The evolutionary ecology of seed size. In ‘Seeds, the ecology of regeneration in plant communities’. 2nd edn (Ed. M Fenner) pp. 31–57. (CABI Publishing: Wallingford, UK)

Liu XJ, Zhang Y, Han WX, Tang AH, Shen JL, Cui ZL, Vitousek P, Erisman JW, Goulding K, Christie P, Fangmeier A, Zhang FS (2013) Enhanced nitrogen deposition over China. Nature 494, 459–462.
Enhanced nitrogen deposition over China.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjtFSktrc%3D&md5=23d3e28bdea6614cdc03c328c2924d6eCAS |

Lloyd DG (1987) Selection of offspring size at independence and other size-versus-number strategies. American Naturalist 129, 800–817.
Selection of offspring size at independence and other size-versus-number strategies.Crossref | GoogleScholarGoogle Scholar |

Maguire JD (1962) Speed of germination–aid in selection and evaluation for seeding emergence and vigor. Crop Science 2, 176–177.
Speed of germination–aid in selection and evaluation for seeding emergence and vigor.Crossref | GoogleScholarGoogle Scholar |

Metcalfe DJ, Grubb PJ (1997) The responses to shade of seedlings of very small-seeded tree and shrub species from tropical rain forest in Singapore. Functional Ecology 11, 215–221.
The responses to shade of seedlings of very small-seeded tree and shrub species from tropical rain forest in Singapore.Crossref | GoogleScholarGoogle Scholar |

Miao SL, Bazzaz FA, Primack RB (1991) Effects of maternal nutrient pulse on reproduction of two colonizing Plantago species. Ecology 72, 586–596.
Effects of maternal nutrient pulse on reproduction of two colonizing Plantago species.Crossref | GoogleScholarGoogle Scholar |

Mo JM, Li DJ, Gundersen P (2008) Seedling growth response of two tropical tree species to nitrogen deposition in southern China. European Journal of Forest Research 127, 275–283.
Seedling growth response of two tropical tree species to nitrogen deposition in southern China.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXps1WisL8%3D&md5=364423a960c5f7b47e2b950c911c3eb7CAS |

Moles AT, Westoby M (2004) Seedling survival and seed size: a synthesis of the literature. Journal of Ecology 92, 372–383.
Seedling survival and seed size: a synthesis of the literature.Crossref | GoogleScholarGoogle Scholar |

Paolini R, Rrincipi M, Froud-Williams RJ, Del PS, Biancardi E (1999) Competition between sugarbeet and Sinapis arvensis and Chenopodium album, as affected by timing of nitrogen fertilization. Weed Research 39, 425–440.
Competition between sugarbeet and Sinapis arvensis and Chenopodium album, as affected by timing of nitrogen fertilization.Crossref | GoogleScholarGoogle Scholar |

Phoenix PB, Hicks WK, Cinderby S, Kuylenstierna JCI, Stock WD, Dentener FJ, Giller KE, Austin AT, Lefroy RB, Gimeno BS, Ashmore MR, Ineson P (2006) Atmospheric nitrogen deposition in world biodiversity hotspots: the need for a greater global perspective in assessing in assessing N deposition impacts. Global Change Biology 12, 470–476.
Atmospheric nitrogen deposition in world biodiversity hotspots: the need for a greater global perspective in assessing in assessing N deposition impacts.Crossref | GoogleScholarGoogle Scholar |

Richter DD, Burrows JP, Nü BH, Granier C, Niemeier U (2005) Increase in tropospheric nitrogen dioxide over China observed from space. Nature 437, 129–132.
Increase in tropospheric nitrogen dioxide over China observed from space.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXpslaltr8%3D&md5=bfa379d2cb36481bac8d5cdd7eebda2cCAS |

Roach DA, Wulff RD (1987) Maternal effects in plants. Annual Review of Ecology and Systematics 18, 209–235.
Maternal effects in plants.Crossref | GoogleScholarGoogle Scholar |

Sargent RD, Goodwillie C, Kalisz S, Ree RH (2007) Phylogenetic evidence for a flower size and number trade-off. American Journal of Botany 94, 2059–2062.
Phylogenetic evidence for a flower size and number trade-off.Crossref | GoogleScholarGoogle Scholar | 21636399PubMed |

Stanton ML (1984) Seed variation in wild radish: effect of seed size on components of seedling and adults fitness. Ecology 65, 1105–1112.
Seed variation in wild radish: effect of seed size on components of seedling and adults fitness.Crossref | GoogleScholarGoogle Scholar |

Susko DJ, Cavers PB (2008) Seed size effects and competitive ability in Thlaspi arvense L. (Brassicaceae). Botany 86, 259–267.
Seed size effects and competitive ability in Thlaspi arvense L. (Brassicaceae).Crossref | GoogleScholarGoogle Scholar |

Vázquez-Yanes C, Orozco-Segovia A (1984) Ecophysiology of seed germination in the tropical humid forests of the world: a review. In ‘Physiological ecology of plants of the wet tropics’. (Eds E Medina, HA Mooney, C Vázquez-Yanes) pp. 37–50. (Dr W. Junk Publishers: The Hague, The Netherlands)

Venable DL (1992) Size-number trade-offs and the variation of seed size with plant resource status. American Naturalist 140, 287–304.
Size-number trade-offs and the variation of seed size with plant resource status.Crossref | GoogleScholarGoogle Scholar |

Venable DL, Brown JS (1988) The selective interactions of dispersal, dormancy, and seed size as adaptations for reducing risk in variable environments. American Naturalist 131, 360–383.
The selective interactions of dispersal, dormancy, and seed size as adaptations for reducing risk in variable environments.Crossref | GoogleScholarGoogle Scholar |

Violle C, Castro H, Richarte J, Navas ML (2009) Intraspecific seed trait variations and competition: passive or adaptive response? Functional Ecology 23, 612–620.
Intraspecific seed trait variations and competition: passive or adaptive response?Crossref | GoogleScholarGoogle Scholar |

Warton DI, Wright IJ, Falster DS, Westoby M (2006) Bivariate line-fitting methods for allometry. Biological Reviews of the Cambridge Philosophical Society 81, 259–291.
Bivariate line-fitting methods for allometry.Crossref | GoogleScholarGoogle Scholar | 16573844PubMed |

Westoby M, Jurado E, Leishman MR (1992) Comparative evolutionary ecology of seed size. Trends in Ecology & Evolution 7, 368–372.
Comparative evolutionary ecology of seed size.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M7itVyjsg%3D%3D&md5=799c831dc655ab29df01a83d164d4d62CAS |

Zhang Y, Liu XJ, Ju XT, Zou GY, Hu KL (2006) Spatial and temporal variation of atmospheric nitrogen deposition in the North China Plain. Acta Ecologica Sinica 26, 1633–1638.
Spatial and temporal variation of atmospheric nitrogen deposition in the North China Plain.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XnvVelt7g%3D&md5=2f0bb094c7a51d89446a7270dc929c8fCAS |

Zhang Y, Dore AJ, Ma L, Liu XJ, Ma WQ, Cape JN, Zhang FS (2010) High resolution inventory of agricultural ammonia emissions in North China Plain. Environmental Pollution 158, 490–501.
High resolution inventory of agricultural ammonia emissions in North China Plain.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsFyks7fO&md5=19abdddb54296ea0746b7ead835f4bb8CAS | 19796855PubMed |

Zheng HY, Li JD (1999) Form and dynamic trait of halophyte community. In ‘Saline plants in Songnen Plain and restoration of alkaline-saline grass’. (Eds HY Zheng, JD Li) pp. 137–138. (Science Press: Beijing)