Abstract
Of the various colorful plant/animal communication systems, adaptive color changes are known to take part in the two extensively studied gene dispersal systems: pollination by both invertebrates and vertebrates and seed dispersal via frugivory. Young and still unrewarding animal-pollinated flowers and young and unripe fleshy fruits are usually green and cryptic. Many flowers become colorful and visually conspicuous only towards anthesis, when they open and offer nectar and/or pollen, or other rewards to pollinators, because their still immature colorful petals are commonly covered by bracts or by green sepals. Many flowers retain their conspicuous advertising colors till they wilt. However, post-pollination floral color change is a well-documented phenomenon in various taxa and life forms on all continents except for Antarctica (Weiss 1991, 1995; Weiss and Lamont 1997; Bradshaw and Schemske 2003). Color change of individual flowers in an inflorescence may reduce their advertising intensity, and thus their detectability by pollinators. Retaining the attractive coloration after pollination, or after they turn unreceptive, may reduce pollinator visits to un-pollinated flowers because the pollinators learn that there is no reward and fly to other plants, thus diminishing the plant’s reproductive success. By the simultaneous reduction of both the reward after pollination and of attractiveness (advertisement) by changing their color, plants direct their pollinators to un-pollinated flowers within the same inflorescence or plant.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Archetti M (2000) The origin of autumn colours by coevolution. J Theor Biol 205:625–630
Archetti M, Döring TF, Hagen SB, Hughes NM, Leather SR, Lee DW, Lev-Yadun S, Manetas Y, Ougham HJ, Schaberg PG, Thomas H (2009a) Unravelling the evolution of autumn colours: an interdisciplinary approach. Trends Ecol Evol 24:166–173
Bradshaw HD Jr, Schemske DW (2003) Allele substitution at a flower colour locus produces a pollinator shift in monkeyflowers. Nature 426:176–178
Brooks R, Owen-Smith N (1994) Plant defences against mammalian herbivores: are juvenile Acacia more heavily defended than mature trees? Bothalia 24:211–215
Clement CR, Manshardt RM (2000) A review of the importance of spines for pejibaye heart-of-palm production. Sci Hortic 83:11–23
Cooper SM, Owen-Smith N (1986) Effects of plant spinescence on large mammalian herbivores. Oecologia 68:446–455
Cornett JW (1986) Spineless petioles in Washingtonia filifera (Arecaceae). Madrono 33:76–78
Gowda JH, Palo RT (2003) Age-related changes in defensive traits of Acacia tortilis Hayne. Afr J Ecol 41:218–223
Hamilton WD, Brown SP (2001) Autumn tree colours as a handicap signal. Proc R Soc Lond B 268:1489–1493
Hoch WA, Zeldin EL, McCown BH (2001) Physiological significance of anthocyanins during autumnal leaf senescence. Tree Physiol 21:1–8
Kozlowski TT (1971) Growth and development of trees, vol I. Academic Press, New York
Lev-Yadun S, Gould KS (2007) What do red and yellow autumn leaves signal? Bot Rev 73:279–289
Lev-Yadun S, Ne’eman G (2006) Color changes in old aposematic thorns, spines, and prickles. Isr J Plant Sci 54:327–333
Milewski AV, Young TP, Madden D (1991) Thorns as induced defenses: experimental evidence. Oecologia 86:70–75
Perevolotsky A, Haimov Y (1991) Structural response of Mediterranean woodland species to disturbance: evidence of different defense strategies. Isr J Bot 40:305–313
Ridley HN (1930) The dispersal of plants throughout the world. L. Reeve & Co Ltd, Ashford
Schaefer HM, Ruxton GD (2011) Plant-animal communication. Oxford University Press, New York
Schaefer HM, Schaefer V (2007) The evolution of visual fruit signals: concepts and constraints. In: Dennis AJ, Schupp EW, Green R, Wescott DW (eds) Seed dispersal: theory and its application in a changing world. CAB International, Wallingford, pp 59–77
Snow B, Snow D (1988) Birds and berries. A study of an ecological interaction. T. & A. D. Poyser, Calton
van der Pijl L (1982) Principles of dispersal in higher plants, 3rd edn. Springer-Verlag, Berlin
Weiss MR (1991) Floral colour changes as cues for pollinators. Nature 354:227–229
Weiss MR (1995) Floral colour change: a widespread functional convergence. Am J Bot 82:167–195
Weiss MR, Lamont BB (1997) Floral colour change and insect pollination: a dynamic relationship. Isr J Plant Sci 45:185–199
White PS (1988) Prickle distribution in Aralia spinosa (Araliaceae). Am J Bot 75:282–285
Willson MF, Whelan CJ (1990) The evolution of fruit color in fleshy-fruited plants. Am Nat 136:790–809
Young TP, Okello BD (1998) Relaxation of an induced defense after exclusion of herbivores: spines on Acacia drepanolobium. Oecologia 115:508–513
Young TP, Stanton ML, Christian CE (2003) Effects of natural and simulated herbivory on spine lengths of Acacia drepanolobium in Kenya. Oikos 101:171–179
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2016 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Lev-Yadun, S. (2016). Color Changes in Old Aposematic Thorns, Spines, and Prickles. In: Defensive (anti-herbivory) Coloration in Land Plants. Springer, Cham. https://doi.org/10.1007/978-3-319-42096-7_28
Download citation
DOI: https://doi.org/10.1007/978-3-319-42096-7_28
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-42094-3
Online ISBN: 978-3-319-42096-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)