Skip to main content
Log in

Relationship Among Phenolic Contents, Seed Predation, and Physical Seed Traits in Mimosa bimucronata Plants

  • ORIGINAL RESEARCH
  • Published:
Journal of Plant Biology Aims and scope Submit manuscript

Abstract

Phenolic contents were compared between Mimosa bimucronata seeds from infested and non-infested fruits to assess induced defense response. By measuring leg length of the bruchid beetle Acanthoscelides schrankiae, we verified whether phenolic contents affected bruchid body size. In addition, the relationship between physical seed traits and phenolic contents was examined. Results showed that seeds from infested fruits had significantly greater phenolic contents than seeds from non-infested fruits, which suggested induced defense. Body size variation in A. schrankiae was marginally nonsignificant according to phenolic contents among plants (negative trend), indicating that phenols may interfere directly with bruchid performance. Seeds that were more irregularly shaped had significantly greater phenolic contents than those that were more uniform. Therefore, the most perfectly spherical seeds may be more vulnerable to seed predation, and our results suggest that the production of phenolic compounds was increased in infested fruits, which in turn may affect A. schrankiae development.

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.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Bekker RM, Bakker JP, Grandin U, Kalamees R, Milberg P, Poschlod P, Thompson K, Willems JH (1998) Seed size, shape and vertical distribution in the soil: indicators of seed longevity. Funct Ecol 12:834–842

    Article  Google Scholar 

  • Boughdad A, Gillon Y, Cagnepain C (1986) Effect of condensed tannins of horse bean husks (Vicia faba) on larval development of Callosobruchus maculatus. Entomol Exp Appl 42:125–132

    Article  CAS  Google Scholar 

  • Burkart A (1959) Leguminosae. In: Parodi LR (ed) Enciclopedia Argentina de Agricultura y Jardineria. ACME, Buenos Aires, pp 443–512

    Google Scholar 

  • Cope JM, Fox CW (2003) Oviposition decisions in the seed beetle, Callosobruchus maculatus (Coleoptera: Bruchidae): effects of seed size on superparasitism. J Stored Prod Res 39:355–365

    Article  Google Scholar 

  • Cornelissen T, Stiling P (2005) Perfect is best: low leaf fluctuating asymmetry reduces herbivory by leaf miners. Oecologia 142:46–56

    Article  PubMed  Google Scholar 

  • Cornelissen T, Stiling P, Drake B (2003) Elevated CO2 decreases leaf fluctuating asymmetry and herbivory by leaf miners on two oak species. Global Change Biol 10:27–36

    Article  Google Scholar 

  • Crawley MJ (2007) The R book. Wiley, Chichester

    Book  Google Scholar 

  • Dana W, Ivo W (2008) Computer image analysis of seed shape and seed color for flax cultivar description. Comput Electron Agr 61:126–135

    Article  Google Scholar 

  • Dell'Aquila A (2007) Towards new computer imaging techniques applied to seed quality testing and sorting. Seed Sci Technol 35:519–538

    Google Scholar 

  • Fineblum WL, Rausher MD (1995) Tradeoff between resistance and tolerance to herbivore damage in a morning glory. Nature 377:517–520

    Article  CAS  Google Scholar 

  • Folin O, Ciocalteau V (1927) On tyrosine and tryptophane determination in proteins. J Biol Chem 73:424–427

    Google Scholar 

  • Fowler SV, Lawton JH (1985) Rapidly induced defenses and talking trees: the devil's advocate position. Amer Nat 126:181–195

    Article  Google Scholar 

  • Fox CW, Mousseau TA (1996) Larval host plant affects fitness consequences of egg size variation in the seed beetle Stator limbatus. Oecologia 107:541–548

    Article  Google Scholar 

  • Fox CW, Waddell KJ, Mousseau TA (1994) Host-associated fitness variation in a seed beetle (Coleoptera: Bruchidae): evidence for local adaptation to a poor quality host. Oecologia 99:329–336

    Article  Google Scholar 

  • Funes G, Basconcelo S, Dias S, Cabido M (1999) Seed size and shape are good predictors of seed persistence in soil in temperate mountain grasslands of Argentina. Seed Sci Res 9:341–345

    Article  Google Scholar 

  • Gianoli E, Suárez LH, Gonzáles WL, González-Teuber M, Acuña-Rodrígues IS (2007) Host-associated variation in sexual size dimorphism and fitness effects of adult feeding in a bruchid beetle. Entomol Exp Appl 122:233–237

    Article  Google Scholar 

  • Grubb PJ, Metcalfe DJ, Grubb EAA, Jones GD (1998) Nitrogen-richness and protection of seeds in Australian tropical rainforest: a test of plant defence theory. Oikos 82:467–482

    Article  Google Scholar 

  • Hagen SB, Folstad I, Jakobsen SW (2003) Autumn colouration and herbivore resistance in mountain birch (Betula pubescens). Ecol Lett 6:807–811

    Article  Google Scholar 

  • Harper JL, Lovell PH, Moore KG (1970) The shapes and sizes of seeds. Annu Rev Ecol Syst 1:327–356

    Article  Google Scholar 

  • Hu WT, Lan YC, Horng SB (1995) Effects of bean size on larval competition and oviposition preference of Callosobruchus maculatus. Chinese J Entomol 15:321–332

    Google Scholar 

  • Hu ZH, Shen YB, Luo YQ, Shen FY, Gao HB, Gao RF (2008) Aldehyde volatiles emitted in succession from mechanically damaged leaves of poplar cuttings. J Plant Biol 51:269–275

    Article  Google Scholar 

  • Hulme PE, Benkman CW (2002) Granivory. In: Herrera CM, Pellmyr O (eds) Plant-animal interactions: an evolutionary approach. Blackwell, Oxford, pp 132–154

    Google Scholar 

  • Illipronti Jr RA, Langerak CJ, Lommen WJM (1997) Variation in and relationships between physical and physiological seed attributes within a soybean seed lot. Seed Sci Technol 25:215–231

    Google Scholar 

  • Illipronti Jr RA, Langerak CJ, Lommen WJM (1999) Variation in physical seed attributes relates to variation in growth of soybean seedlings within a seed lot. Seed Sci Technol 27:339–357

    Google Scholar 

  • Janzen DH (1969) Seed-eaters versus seed size, number, toxicity and dispersal. Evolution 23:1–27

    Article  Google Scholar 

  • Janzen DH (1971) Seed predation by animals. Annu Rev Ecol Syst 2:465–492

    Article  Google Scholar 

  • Janzen DH (1980) Specificity of seed-attacking beetles in a Costa Rican deciduous forest. J Ecol 68:929–952

    Article  Google Scholar 

  • Johnson CD (1983) Ecosystematics of Acanthoscelides (Coleoptera: Bruchidae) of southern Mexico and Central America. Misc Publ Entomol Soc Amer 56:1–248

    Google Scholar 

  • Johnson CD (1990) Systematics of the seed beetle genus Acanthoscelides (Bruchidae) of northern South America. Trans Am Entomol Soc 116:297–618

    Google Scholar 

  • Jolivet P (1998) Interrelationship between insects and plants. CRC, Boca Raton

    Google Scholar 

  • Karban R, Baldwin IT (1997) Induced responses to herbivory. University of Chicago Press, Chicago

    Google Scholar 

  • Klug-Pumpel B, Scharfetter-Lehrl G (2008) Soil diaspore reserves above the timberline in the Austrian Alps. Flora 203:292–303

    Google Scholar 

  • Kollmann J, Coomes DA, White SM (1998) Consistencies in post-dispersal seed predation of temperate fleshy-fruited species among seasons, years and sites. Funct Ecol 12:683–690

    Article  Google Scholar 

  • Lorenzi H (2000) Plantas Daninhas do Brasil: Terrestres, Aquáticas, Parasitas e Tóxicas. Instituto Plantarum, Nova Odessa

    Google Scholar 

  • Matilla A, Gallardo M, Puga-Hermida MI (2005) Structural, physiological and molecular aspects of heterogeneity in seeds: a review. Seed Sci Res 15:63–76

    Article  CAS  Google Scholar 

  • Moles AT, Westoby M (2004) Seedling survival and seed size: a synthesis of the literature. J Ecol 92:372–383

    Article  Google Scholar 

  • Moles AT, Westoby M (2006) Seed size and plant strategy across the whole life cycle. Oikos 113:91–105

    Article  Google Scholar 

  • Moles AT, Hodson DW, Webb CJ (2000) Seed size and shape and persistence in the soil in the New Zealand flora. Oikos 89:541–545

    Article  Google Scholar 

  • Møller AP (1995) Leaf-mining insects and fluctuating asymmetry in Ulmus glabra leaves. J Anim Ecol 64:697–707

    Article  Google Scholar 

  • Nápoles JR (2002) Bruchidae. In: Bousquets, JL, Morrone JJ (eds), Biodiversidad, Taxonomía y Biogeografía de Artrópodos de México: Hacia Una Síntesis de su Conocimiento, vol 3. Unan, pp. 513-534

  • Or K, Ward D (2004) The effects of seed quality and pipecolic and djenkolic acids on bruchid beetle infestation in water deficit-stressed Acacia trees. J Chem Ecol 30:2297–2307

    Article  CAS  PubMed  Google Scholar 

  • Parsons PA (1990) Fluctuating asymmetry: an epigenetic measure of stress. Biol Rev 65:131–145

    Article  CAS  PubMed  Google Scholar 

  • Puerta-Piñero C, Gómez JM, Hódar JA (2008) Shade and herbivory induce fluctuating asymmetry in a Mediterranean oak. Int J Plant Sci 169:631–635

    Article  Google Scholar 

  • Rohner C, Ward D (1997) Chemical and mechanical defenses against herbivory in two sympatric species of desert Acacia. J Veg Sci 8:717–726

    Article  Google Scholar 

  • Schoonhoven LM, van Loon JJA, Dicke M (2005) Insect–plant biology. Oxford University Press, New York

    Google Scholar 

  • Schultz JC, Baldwin IT (1982) Oak leaf quality declines in response to defoliation by gypsy moth larvae. Science 217:149–151

    Article  PubMed  Google Scholar 

  • Silva LA, Maimoni-Rodella RCS, Rossi MN (2007) A preliminary investigation of pre-dispersal seed predation by Acanthoscelides schrankiae Horn (Coleoptera: Bruchidae) in Mimosa bimucronata (DC.) Kuntze trees. Neotrop Entomol 36:197–202

    PubMed  Google Scholar 

  • Southgate BJ (1979) Biology of the Bruchidae. Annu Rev Entomol 24:449–473

    Article  Google Scholar 

  • Szentesi A, Jermy T (1995) Predispersal seed predation in leguminous species: weed morphology and bruchid distribution. Oikos 73:23–32

    Article  Google Scholar 

  • Thanthianga C, Mitchell R (1990) The fecundity and oviposition behavior of South Indian strain Callosobruchus maculatus. Entomol Exp Appl 57:133–142

    Article  Google Scholar 

  • Thiery D, Jarry M, Pouzat J (1994) To penetrate or not to penetrate—a behavioral choice by bean beetle 1st instar larvae in response to Phaseolus vulgaris seed surface quality. J Chem Ecol 20:1867–1875

    Article  Google Scholar 

  • Thompson K, Grime JP (1979) Seasonal variation in the seed banks of herbaceous species in ten contrasting habitats. J Ecol 67:893–921

    Article  Google Scholar 

  • Timms R (1998) Size-independent effects of larval host on adult fitness in Callosobruchus maculatus. Ecol Entomol 23:480–483

    Article  Google Scholar 

  • Tomaz CA, Kestring D, Rossi MN (2007) Effects of the seed predator Acanthoscelides schrankiae on viability of its host plant Mimosa bimucronata. Biol Res 40:281–290

    Article  PubMed  Google Scholar 

  • Tracy M, Freeman DC, Dude JL, Miglia KJ, Gram JH, Hough RA (2003) Developmental instability: an appropriate indicator of plant fitness components? In: Polak M (ed) Developmental instability: causes and consequences. Oxford University Press, New York, pp 196–212

    Google Scholar 

  • van Huis A, de Rooy M (1998) The effect of leguminous plant species on Callosobruchus maculatus (Coleoptera: Bruchidae) and its egg parasitoid Uscana lariophaga (Hymenoptera: Trichogrammatidae). B Entomol Res 88:93–99

    Article  Google Scholar 

  • Yang RL, Horng SB (2002) Host size discrimination and oviposition behavior of the seed beetle, Callosobruchus maculatus (F.). Formos Entomol 22:343–357

    Google Scholar 

  • Yang RL, Fushing H, Horng SB (2006) Effects of search experience in a resource-heterogeneous environment on the oviposition decision of the seed beetle, Callosobruchus maculatus (F.). Ecol Entomol 31:285–293

    Article  Google Scholar 

  • Zar JH (1999) Biostatistical analysis. Prentice Hall, Upper Saddle River

    Google Scholar 

  • Zvereva E, Kozlov M, Haukioja E (1997) Stress responses of Salix borealis to pollution and defoliation. J Appl Ecol 34:1387–1396

    Article  Google Scholar 

Download references

Acknowledgments

We thank Professors Janet W. Reid and James Welsh for English assistance with the manuscript text. D. Kestring is grateful to CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico). L. C. C. R. de Menezes (05/57999-3), C. A. Tomaz (04/10329-0) and M. N. Rossi (04/06737-6) thank Fapesp (Fundação de Amparo à Pesquisa do Estado de São Paulo) for financial support. We are most grateful to Jeferson Klein for technical assistance.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Débora Kestring.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kestring, D., Menezes, L.C.C.R., Tomaz, C.A. et al. Relationship Among Phenolic Contents, Seed Predation, and Physical Seed Traits in Mimosa bimucronata Plants. J. Plant Biol. 52, 569–576 (2009). https://doi.org/10.1007/s12374-009-9073-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12374-009-9073-3

Keywords

Navigation