Abstract
Emergence time and population density both have important influences on plants, but their interactive effects have not been well understood, especially on plant reproduction in dynamic patterns. A field experiment was conducted by subjecting plants of Abutilon theophrasti Medicus (Malvaceae) to four treatments of sowing dates (emergence periods, ET1–ET4) and three treatments of (low, medium and high) planting density, and population reproductive traits such as the number of reproductive individuals in total and of different reproductive ranks (RR) were observed, and mean values and among-individual variation in these traits were calculated. Results showed that either an advance or delay of emergence can increase the percentage of flowering or fruiting individuals of the populations. Compared to low density, high density reduced the percentage of flowering individuals and the number of fruits per individual at day 110, with little effect on the percentage of fruiting individuals, whereas medium density promoted the reproduction, for populations of ET1. Density effects were only significant for the plants that emerged early, and increased density reduced the responses of plants to emergence time. The results revealed the strategies of A. theophrasti in dealing with complex biotic environmental changes at the population level: advanced or delayed emergence can result in shortened vegetative growth and earlier reproduction, whereas increased density tended to decrease the percentage of flowering individuals while maintaining that of fruiting ones stable and effects density depend on the strength of inter-plant interactions.
Similar content being viewed by others
References
Abe M, Honda A, Hoshizaki K, Miguchi H (2008) Advantage of early seedling emergence in Fagus crenata: importance of cotyledon stage for predator escape and pathogen avoidance. Ecol Res 23:681–688
Afonso A, Castro S, Loureiro J, Mota L, Cerca de Oliveira J, Torices R (2014) The effects of achene type and germination time on plant performance in the heterocarpic Anacyclus clavatus (Asteraceae). Am J Bot 101:892–898
Bianchi E, Bugmann H, Bigler C (2019) Early emergence increases survival of tree seedlings in Central European temperate forests despite severe late frost. Ecol Evol 9:8238–8252
Burghardt LT, Metcalf CJE, Wilczek AM, Schmitt J, Donohue K (2015) Modeling the influence of genetic and environmental variation on the expression of plant life cycles across landscapes. Am Nat 185:212–227
Casper BB, Jackson RB (1997) Plant competition underground. Ann Rev Ecol Syst 28:545–570
Cogoni D, Fenu G, Bacchetta G (2013) Effects of timing of emergence and microhabitat conditions on the seedling performance of a coastal Mediterranean plant. Ecoscience 20:131–136
Donohue K (2003) Setting the stage: phenotypic plasticity as habitat selection. Int J Plant Sci 164:S79–S92
Donohue K (2005) Niche construction through phenological plasticity: life history dynamics and ecological consequences. New Phytol 166:83–92
Donohue K (2014) Why ontogeny matters during adaptation: developmental niche construction and pleiotorpy across the life cycle in Arabidopsis thaliana. Evolution 68:32–47
Donohue K, Dorn D, Griffith C, Kim E, Aguilera A, Polisetty CR, Schmitt J (2005) Niche construction through germination cueing: life-history responses to timing of germination in Arabidopsis thaliana. Evolution 59:771–785
Donohue K, de Casas RR, Burghardt L, Kovach K, Willis CG (2010) Germination, postgermination adaptation, and species ecological ranges. Ann Rev Ecol Evol Syst 41:293–319
Dyer A, Fenech A, Rice KJ (2000) Accelerated seedling emergence in interspecific competitive neighbourhoods. Ecol Lett 3:523–529
Forster MA, Ladd B, Bonser SP (2011) Optimal allocation of resources in response to shading and neighbours in the heteroblastic species, Acacia implexa. Ann Bot 107:219–228
Foxx AJ, Fort F (2019) Root and shoot competition lead to contrasting competitive outcomes under water stress: a systematic review and meta-analysis. PLoS ONE 14:1–17
Hutchings MJ, Budd CSJ (1981) Plant competition and its course through time. Bioscience 31:640–645
Japhet W, Zhou D, Zhang H, Zhang H, Yu T (2009) Evidence of phenotypic plasticity in the response of Fagopyrum esculentum to population density and sowing date. J Plant Biol 52:303–311
Kelly MG, Levin DA (1997) Fitness consequences and heritability aspects of emergence date in Phlox drummondii. J Ecol 85:755–766
March-Salas M, Fandos G, Fitze PS (2021) Effects of intrinsic environmental predictability on intra-individual and intra-population variability of plant reproductive traits and eco-evolutionary consequences. Ann Bot 127:413–423
McConnaughay KDM, Bazzaz FA (1992) The occupation and fragmentation of space: consequences of neighbouring shoots. Func Ecol 6:711–718
McConnaughay KDM, Coleman JS (1999) Biomass allocation in plants: ontogeny or optimality? A test along three resource gradients. Ecology 80:2581–2593
Mercer KL, Alexander HM, Snow AA (2011) Selection on seedling emergence timing and size in an annual plant, Helianthus Annuus (Common Sunflower, Asteraceae). Am J Bot 98:975–985
Metcalf JC, Rose KE, Rees M (2003) Evolutionary demography of monocarpic perennials. Trends Ecol Evol 18:471–480
Poorter H, Niklas KJ, Reich PB, Oleksyn J, Poot P, Mommer L (2012) Biomass allocation to leaves, stems and roots: meta-analyses of interspecific variation and environmental control. New Phytol 193:30–50
Sadras VO, Bange MP, Milroy SP (1997) Reproductive allocation of cotton in response to plant and environmental factors. Ann Bot 80:75–81
Seiwa K (2000) Effects of seed size and emergence time on tree seedling establishment: importance of developmental constraints. Oecologia 123:208–215
Stratton DA (1992) Life-cycle components of selection in Erigeron annuus: I. Phenotypic selection. Evolution 46:92–106
Tuljapurkar S (1990) Delayed reproduction and fitness in variable environments. Proc Nat Acad Sci USA 87:1139–1143
Verdú M, Traveset A (2005) Early emergence enhances plant fitness: a phylogenetically controlled meta-analysis. Ecology 86:1385–1394
Violle C, Enquist BJ, McGill BJ, Jiang LIN, Albert CH, Hulshof C, Jung V, Messier J (2012) The return of the variance: intraspecific variability in community ecology. Trends Ecol Evol 27:244–252
Wang S, Zhou D-W (2021) Stage-dependent plasticity in biomass allocation and allometry in response to population density in Abutilon theophrasti: a step forward to understanding the nature of phenotypic plasticity. Plant Ecol 222:1157–1181
Wang S, Zhou D-W (2022) Architectural plasticity in response to population density in Abutilon theophrasti (Malvaceae). Ecol Res 37:228–239
Wang T-H, Zhou D-W, Wang P, Zhang H-X (2006) Size-dependent reproductive effort in Amaranthus retroflexus: the fluence of planting density and sowing date. Can J Bot 84:485–492
Wang S, Li L, Zhou D-W (2017) Morphological plasticity in response to population density varies with soil conditions and growth stage in Abutilon theophrasti (Malvaceae). Plant Ecol 218:785–797
Wang S, Li L, Zhou D-W (2021) Root morphological responses to population density vary with soil conditions and growth stages: the complexity of density effects. Ecol Evol 11:10590–10599
Wilczek AM, Roe JL, Knapp MC, Cooper MD, Lopez-Gallego C, Martin LJ, Muir CD, Sim S, Walker A, Anderson J, Egan JF, Moyers BT, Petipas R, Giakountis A, Charbit E, Coupland G, Welch SM, Schmitt J (2009) Effects of genetic perturbation on seasonal life history plasticity. Science 323:930–934
Zhou D-W, Wang T-H, Valentine I (2005) Phenotypic plasticity of life-history characters in response to different germination timing in two annual weeds. Can J Bot 83:28–36
Acknowledgements
We are grateful to the reviewers and editors who all provided useful feedback on this manuscript.
Funding
This work was funded by the National Natural Science Foundation of China (NSFC, 31800335, 32171511), Guizhou Province Science and Technology Department (2019-1089) and Guizhou University Talent Introduction Research Program (2017-39) to SW.
Author information
Authors and Affiliations
Contributions
SW and D-WZ conceived and designed the experiment. SW carried out the experiments, analyzed the data, prepared the figures and tables and wrote and reviewed the drafts of the paper. Both authors approved the final draft.
Corresponding author
Ethics declarations
Conflict of interest
No conflict of interest have been declared.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Wang, S., Zhou, DW. Dynamic reproductive plasticity in response to emergence time and population density in Abutilon theophrasti (Malvaceae). Braz. J. Bot 45, 1057–1066 (2022). https://doi.org/10.1007/s40415-022-00814-3
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40415-022-00814-3