Defensive functions of white coloration in coastal and dune plants

References

• Allen, J.A., Knill, R. 1991. Do grazers leave mottled leaves in the shade? Trends Ecol. Evol. 6: 109-110.
   Google Scholar
• Archetti, M. 2000. The origin of autumn colours by coevolution. J. Theor. Biol. 205: 625-630.
   Google Scholar
• Baker, G., Jones, L.H.P., Wardrop, I.D. 1959. Cause of wear in sheeps' teeth. Nature 184: 1583-1584.
   Google Scholar
• Ballaré, C.L. 2003. Stress under the sun: spotlight on ultraviolet-B responses. Plant Physiol. 132: 1725-1727.
   Google Scholar
• Barlow, B.A., Wiens, D. 1977. Host-parasite resemblance in Australian mistletoes: the case for cryptic mimicry. Evolution 31: 69-84.
   Google Scholar
• Benson, L. 1982. The cacti of the United States and Canada. Stanford University Press, Stanford, CA.
   Google Scholar
• Benzing, D.H. 2000. Bromeliaceae: profile of an adaptive radiation. Cambridge University Press, Cambridge.
   Google Scholar
• Borowicz, V.A. 1988. Do vertebrates reject decaying fruit? An experimental test with Cornus amomum fruits. Oikos 53: 74-78.
   Google Scholar
• Brandt, M., Mahsberg, D. 2002. Bugs with a backpack: the function of nymphal camouflage in the West African assassin bugs Paredocla and Acanthaspis spp. Anim. Behav. 63: 277-284.
   Google Scholar
• Brayton, R.D., Capon, B. 1980. Productivity, depletion, and natural selection of Salvia columbariae seeds. Aliso 9: 581-587.
   Google Scholar
• Breen, J.P. 1994. Acremonium endophyte interactions with enhanced plant resistance to insects. Annu. Rev. Entomol. 39: 401-423.
   Google Scholar
• Briscoe, A.D., Chittka, L. 2001. The evolution of color vision in insects. Annu. Rev. Entomol. 46: 471-510.
   Google Scholar
• Buchholz, R., Levey, D.J. 1990. The evolutionary triad of microbes, fruits, and seed dispersers: an experiment in fruit choice by cedar waxwings, Bombycilla cedrorum.Oikos 59: 200-204.
   Google Scholar
• Cahn, M.G., Harper, J.L. 1976. The biology of the leaf mark polymorphism in Trifolium repens L. 2. Evidence for the selection of leaf marks by rumen fistulated sheep. Heredity 37: 327-333.
   Google Scholar
• Caro, T. 2005. Antipredator defenses in birds and mammals. University of Chicago Press, Chicago.
   Google Scholar
• Chittka, L. 1997. Bee color vision is optimal for coding flower color, but flower colors are not optimal for being coded—why? Isr. J. Plant Sci. 45: 115-127.
   Google Scholar
• Clay, K. 1988. Clavicipitaceous fungal endophytes of grasses: coevolution and the change from parasitism to mutualism. In: Pirozynski, K.A., Hawksworth, D.L., eds. Coevolution of fungi with plants and animals. Academic Press, London, pp. 79-105.
   Google Scholar
• Clay, K. 1990. Fungal endophytes of grasses. Annu. Rev. Ecol. Syst. 21: 275-297.
   Google Scholar
• Cloudsley-Thompson, J.L. 1979. Adaptive functions of the colours of desert animals. J. Arid Environ. 2: 95-104.
   Google Scholar
• Cloudsley-Thompson, J.L. 1999. Multiple factors in the evolution of animal coloration. Naturwissenschaften 86: 123-132.
   Google Scholar
• Cole, D.T. 1970. Lithops in habitat. In: Sprechman, D.L., ed. Lithops. Fairleigh Dickinson University Press, Cranbury, NJ, pp. 21-32.
   Google Scholar
• Cole, D.T., Cole, N.A. 2005. Lithops—flowering stones. Cactus & Co., Venegono, Italy.
   Google Scholar
• Cook, R.J., Barron, J.C., Papendick, R.I., Williams, G.J.III. 1980. Impact on agriculture of the Mount St. Helens eruptions. Science 211: 16-22.
   Google Scholar
• Cott, H.B. 1940. Adaptive coloration in animals. Methuen, London.
   Google Scholar
• Danin, A. 1996. Plants of desert dunes. Springer Verlag, Berlin.
   Google Scholar
• Domínguez, K., Jiménez, M.-L. 2005. Mating and self-burying behavior of Homalonychus theologus Chamberlin (Araneae, Homalonychidae) in Baja, California sur. J. Arachnol. 33: 167-174.
   Google Scholar
• Dominy, N.D., Lucas, P.W., Ramsden, W., Riba-Hernandez, P., Stoner, K.E., Turner, I.M. 2002. Why are young leaves red? Oikos 98: 163-176.
   Google Scholar
• Ebeling, W. 1971. Sorptive dusts for pest control. Annu. Rev. Entomol. 16: 123-158.
   Google Scholar
• Edmunds, M. 1974. Defence in animals. A survey of antipredator defences. Longman, Harlow, UK.
   Google Scholar
• Ehleringer, J., Björkman, O., Mooney, H.A. 1976. Leaf pubescence: effects on absorptance and photosynthesis in a desert shrub. Science 192: 376-377.
   Google Scholar
• Eisner, T., Eisner, M., Siegler, M. 2005. Secret weapons. Defenses of insects, spiders, scorpions, and other many-legged creatures. Harvard University Press, Cambridge, MA.
   Google Scholar
• Elmi, A.A., West, C.P. 1995. Endophyte infection effects on stomatal conductance, osmotic adjustment, and drought recovery of tall fescue. New Phytol. 131: 61-67.
   Google Scholar
• Endler, J.A. 1978. A predator's view of animal color patterns. Evol. Biol. 11: 319-364.
   Google Scholar
• Endler, J.A. 1984. Progressive background matching in moths, and a quantitative measure of crypsis. Biol. J. Linn. Soc. 22: 187-231.
   Google Scholar
• Fahn, A. 1979. Secretory tissues in plants. Academic Press, London.
   Google Scholar
• Fahn, A. 1988. Secretory tissues in vascular plants. New Phytol. 108: 229-257.
   Google Scholar
• Fahn, A. 1990. Plant anatomy. 4th ed. Pergamon Press, Oxford, UK.
   Google Scholar
• Fahn, A., Cutler, D.F. 1992. Xerophytes. Gebrüder Borntraeger, Berlin.
   Google Scholar
• Fahn, A., Shimony, C. 1996. Glandular trichomes of Fagonia L. (Zygophyllaceae) species: structure, development and secreted materials. Ann. Bot. 77: 25-34.
   Google Scholar
• Fu, H.Y., Chen, S.J., Chen, R.F., Ding, W.H., Kuo-Huang, L.L., Huang, R.N. 2006. Identification of oxalic acid and tartaric acids as major persistent pain-inducing toxins in the stinging hairs of the Nettle, Urtica thunbergiana.Ann. Bot. 98: 57-65.
   Google Scholar
• Givnish, T.J. 1990. Leaf mottling: relation to growth form and leaf phenology and possible role as camouflage. Funct. Ecol. 4: 463-474.
   Google Scholar
• Gould, K.S. 2004. Nature's Swiss army knife: the diverse protective roles of anthocyanins in leaves. J. Biomed. Biotechnol. 2004(5): 314-320.
   Google Scholar
• Grammatikopoulos, G., Karabourniotis, G., Kyparissis, A., Petropoulou, Y., Manetas, Y. 1994. Leaf hairs of olive (Olea europaea) prevent stomatal closure by ultraviolet-B radiation. Aust. J. Plant Physiol. 21: 293-301.
   Google Scholar
• Gressitt, J.L., Sedlacek, J., Szent-Ivany, J.J.H. 1965. Flora and fauna on backs of large Papuan moss-forest weevils. Science 150: 1833-1835.
   Google Scholar
• Halpern, M., Raats, D., Lev-Yadun, S. 2007. Plant biological warfare: thorns inject pathogenic bacteria into herbivores. Environ. Microbiol. 9: 584-592.
   Google Scholar
• Hamilton, W.D., Brown, S.P. 2001. Autumn tree colours as a handicap signal. Proc. R. Soc. Lond. B 268: 1489-1493.
   Google Scholar
• Hamilton, W.J.III. 1973. Life's color code. McGraw-Hill, New York.
   Google Scholar
• Harper, J.L. 1977. Population biology of plants. Academic Press, London.
   Google Scholar
• Heinrich, B. 1993. How avian predators constrain caterpillar foraging. In: Stamp, N.E., Casey, T.M., eds. Caterpillars: ecological and evolutionary constraints on foraging. Chapman & Hall, New York, pp. 224-247.
   Google Scholar
• Herrera, C.M. 1982. Defense of ripe fruit from pests: its significance in relation to plant-disperser interactions. Am. Nat. 120: 218-241.
   Google Scholar
• Hinton, H.E. 1973. Natural deception. In: Gregory, R.L., Gombrich, E.H., eds. Illusion in nature and art. Duckworth, London, pp. 97-159.
   Google Scholar
• Hoekstra, H.E. 2006. Genetics, development and evolution of adaptive pigmentation in vertebrates. Heredity 97: 222-234.
   Google Scholar
• Honkavaara, J., Koivula, M., Korpimäki, E., Siitari, H., Viitala, J. 2002. Ultraviolet vision and foraging in terrestrial vertebrates. Oikos 98: 505-511.
   Google Scholar
• Janzen, D.H. 1977. Why fruits rot, seeds mold, and meat spoils. Am. Nat. 111: 691-713.
   Google Scholar
• Johnson, H.B. 1975. Plant pubescence: an ecological perspective. Bot. Rev. 41: 233-258.
   Google Scholar
• Juniper, B.E. 1994. Flamboyant flushes: a reinterpretation of non-green flush colours in leaves. In: International Dendrology Society Yearbook 1993, pp. 49-57.
   Google Scholar
• Juniper, B.E., Robins, R.J., Joel, D.M. 1989. The carnivorous plants. Academic Press, London.
   Google Scholar
• Justus, M., Witte, L., Hartmann, T. 1997. Levels and tissue distribution of loline alkaloids in endophyte-infected Festuca pratensis.Phytochem. 44: 51-57.
   Google Scholar
• Karageorgou, P., Manetas, Y. 2006. The importance of being red when young: anthocyanins and the protection of young leaves of Quercus coccifera from insect herbivory and excess light. Tree Physiol. 26: 613-621.
   Google Scholar
• Kettlewell, B. 1973. The evolution of melanism. Clarendon Press, Oxford, UK.
   Google Scholar
• Lapointe, S.L. 2000. Particle film deters oviposition by Diaprepes abbreviatus (Coleoptera: Curculionidae). J. Econ. Entomol. 93: 1459-1463.
   Google Scholar
• Lavranos, J.J. 1974. Notes on the succulent flora of north east Africa and southern Arabia. Part II. Cact. Succulent J. (U.S.) 46: 125-130.
   Google Scholar
• Levin, D.A. 1973. The role of trichomes in plant defense. Q. Rev. Biol. 48: 3-15.
   Google Scholar
• Lev-Yadun, S. 2001. Aposematic (warning) coloration associated with thorns in higher plants. J. Theor. Biol. 210: 385-388.
   Google Scholar
• Lev-Yadun, S. 2003. Why do some thorny plants resemble green zebras? J. Theor. Biol. 244: 483-489.
   Google Scholar
• Lev-Yadun, S. 2006. Defensive coloration in plants: a review of current ideas about anti-herbivore coloration strategies. In: Teixeira da Silva, J.A., ed. Floriculture, ornamental and plant biotechnology: advances and topical issues. Vol. IV. Global Science Books, London, pp. 292-299.
   Google Scholar
• Lev-Yadun, S., Ne'eman, G. 2004. When may green plants be aposematic? Biol. J. Linn. Soc. 81: 413-416.
   Google Scholar
• Lev-Yadun, S., Ne'eman, G. 2006. Color changes in old aposematic thorns, spines, and prickles. Isr. J. Plant Sci. 54: 317-325, this issue.
   Google Scholar
• Lev-Yadun, S., Dafni, A., Inbar, M., Izhaki, I., Ne'eman, G. 2002. Colour patterns in vegetative parts of plants deserve more research attention. Trends Plant Sci. 7: 59-60.
   Google Scholar
• Lev-Yadun, S., Dafni, A., Flaishman, M.A., Inbar, M., Izhaki, I., Katzir, G., Ne'eman, G. 2004. Plant coloration undermines herbivorous insect camouflage. BioEssays 26: 1126-1130.
   Google Scholar
• Mainland, I.L. 2003. Dental microwear in grazing and browsing Gotland sheep (Ovis aries) and its implications for dietary reconstruction. J. Archaeol. Sci. 30: 1513-1527.
   Google Scholar
• Majerus, M.E.N. 1998. Melanism. Evolution in action. Oxford University Press, Oxford.
   Google Scholar
• Manetas, Y. 2003. The importance of being hairy: the adverse effects of hair removal on stem photosynthesis of Verbascum speciosum are due to solar UV-B radiation. New Phytol. 158: 503-508.
   Google Scholar
• Manetas, Y. 2006. Why some leaves are anthocyanic and why most anthocyanic leaves are red? Flora 201: 163-177.
   Google Scholar
• Manzur, M.I., Courtney, S.P. 1984. Influence of insect damage in fruits of hawthorn on bird foraging and seed dispersal. Oikos 43: 265-270.
   Google Scholar
• Marquis, R.J., Whelan, C. 1996. Plant morphology and recruitment of the third trophic level: subtle and little-recognized defenses? Oikos 75: 330-334.
   Google Scholar
• Massey, F.P., Hartley, S.E. 2006. Experimental demonstration of the antiherbivore effects of silica in grasses: impacts on foliage digestibility and vole growth rates. Proc. R. Soc. Lond. B 273: 2299-2304.
   Google Scholar
• Midgley, J.J. 2004. Why are spines of African Acacia species white? Afr. J. Range Forage Sci. 21:211-212.
   Google Scholar
• McNaughton, S.J., Tarrants, J.L. 1983. Grass leaf silicification: natural selection for an inducible defense against herbivores. Proc. Natl. Acad. Sci. USA 80: 790-791.
   Google Scholar
• McNaughton, S.J., Tarrants, J.L., McNaughton, M.M., Davis, R.H. 1985. Silica as a defense against herbivory and a growth promotor in African grasses. Ecology 66: 528-535.
   Google Scholar
• Merilaita, S. 1998. Crypsis through disruptive coloration in an isopod. Proc. R. Soc. Lond. B 265: 1059-1064.
   Google Scholar
• Merilaita, S., Lind, J. 2005. Background-matching and disruptive coloration, and the evolution of cryptic coloration. Proc. R. Soc. Lond. B 272: 665-670.
   Google Scholar
• Merilaita, S., Tuomi, J., Jormalainen, V. 1999. Optimization of cryptic coloration in heterogeneous habitat. Biol. J. Linn. Soc. 67: 151-161.
   Google Scholar
• Merilaita, S., Lyytinen, A., Mappes, J. 2001. Selection for cryptic coloration in a visually heterogeneous habitat. Proc. R. Soc. Lond. B 268: 1925-1929.
   Google Scholar
• Meunier, J.D., Colin, F., eds. 2001. Phytoliths: application in earth sciences and human history. A.A. Balkema Publishers, Lisse.
   Google Scholar
• Niemelä, P., Tuomi, J. 1987. Does the leaf morphology of some plants mimic caterpillar damage? Oikos 50: 256-257.
   Google Scholar
• Nystrand, O., Granström, A. 1997. Post-dispersal predation on Pinus sylvestris seeds by Fringilla spp: ground substrate affects selection for seed color. Oecologia 110: 353-359.
   Google Scholar
• Owen, D. 1982. Camouflage and mimicry. University of Chicago Press, Chicago.
   Google Scholar
• Paul, N.D., Gwynn-Jones, D. 2003. Ecological roles of solar UV radiation: towards an integrated approach. Trends Ecol. Evol. 18: 48-55.
   Google Scholar
• Porter, J.K. 1994. Chemical constituents of grass endophytes. In: Bacon, C.W., White, J.F., eds. Biotechnology of endophytic fungi of grasses. CRC Press, Boca Raton, FL, pp. 103-123.
   Google Scholar
• Prokopy, R.J., Owens, E.D. 1983. Visual detection of plants by herbivorous insects. Annu. Rev. Entomol. 28: 337-364.
   Google Scholar
• Prychild, C.J., Rudall, P.J., Gregory, M. 2004. Systematics and biology of silica bodies in Monocotyledons. Bot. Rev. 69: 377-440.
   Google Scholar
• Rapp, G.Jr., Mulholland, S.C., eds. 1992. Phytolith systematics. Emerging issues. Plenum Press, New York.
   Google Scholar
• Rosenblum, E.B. 2006. Convergent evolution and divergent selection: lizards at the white sands ecotone. Am. Nat. 167: 1-15.
   Google Scholar
• Rubino, D.L., McCarthy, B.C. 2004. Presence of aposematic (warning) coloration in vascular plants of southeastern Ohio. J. Torrey Bot. Soc. 131: 252-256.
   Google Scholar
• Ruxton, G.D., Sherratt, T.N., Speed, M.P. 2004. Avoiding attack. The evolutionary ecology of crypsis, warning signals & mimicry. Oxford University Press, Oxford.
   Google Scholar
• Saikkonen, K., Faeth, S.H., Helander, M., Sullivan, T.J. 1998. Fungal endophytes: a continuum of interactions with host plants. Annu. Rev. Ecol. Syst. 29: 319-343.
   Google Scholar
• Sanson, G.D., Kerr, S.A., Gross, K.A. 2007. Do silica phytoliths really wear mammalian teeth? J. Archaeol. Sci. 34: 526-531.
   Google Scholar
• Saracino, A., Pacella, R., Leone, V., Borghetti, M. 1997. Seed dispersal and changing seed characteristics in a Pinus halepensis Mill. forest after fire. Plant Ecol. 130: 13-19.
   Google Scholar
• Saracino, A., D'Alessandro, C.M., Borghetti, M. 2004. Seed colour and post-fire bird predation in a Mediterranean pine forest. Acta Oecol. 26: 191-196.
   Google Scholar
• Schaefer, M., Stobbe, N. 2006. Disruptive coloration provides camouflage independent of background matching. Proc. R. Soc. Lond. B 273: 2427-2432.
   Google Scholar
• Schoener, T.W. 1987. Leaf pubescence in buttonwood: community variation in a putative defense against defoliation. Proc. Natl. Acad. Sci. USA 84: 7992-7995.
   Google Scholar
• Schoener, T.W. 1988. Leaf damage in island buttonwood, Conocarpus erectus: correlations with pubescence, island area, isolation and the distribution of major carnivores. Oikos 53: 253-266.
   Google Scholar
• Shears, J. 1988. The use of a sand-coat in relation to feeding and dial activity in the sepiolid squid Euprymna scolopes. Malacologia 29: 121-133.
   Google Scholar
• Shi, Y., Yokoyama, S. 2003. Molecular analysis of the evolutionary significance of ultraviolet vision in vertebrates. Proc. Natl. Acad. Sci. USA 100: 8308-8313.
   Google Scholar
• Shifriss, O. 1981. Do Cucurbita plants with silvery leaves escape virus infection? Cucurbit Genetics Cooperative, Report 4, pp. 42-43.
   Google Scholar
• Showler, A.T. 2002. Effects of kaolin-based particle film application on boll weevil (Coleoptera: Curculionidae) injury to cotton. J. Econ. Entomol. 95: 754-762.
   Google Scholar
• Showler, A.T. 2003. Effects of kaolin particle film on beet army-worm, Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae), oviposition, larval feeding and development on cotton, Gossypium hirsutumL. Agric., Ecosyst. Environ. 95: 265-271.
   Google Scholar
• Slocum, R.D., Lawrey, J.D. 1976. Viability of the epizoic lichen flora carried and dispersed by green lacewing (Nodita pavida) larvae. Can. J. Bot. 54: 1827-1831.
   Google Scholar
• Smith, A.P. 1986. Ecology of a leaf color polymorphism in a tropical forest species: habitat segregation and herbivory. Oecologia 69: 283-287.
   Google Scholar
• Spaethe, J., Tautz, J., Chittka, L. 2001. Visual constraints in foraging bumblebees: flower size and color affect search time and flight behavior. Proc. Natl. Acad. Sci. USA 98: 3898-3903.
   Google Scholar
• Speed, M.P., Ruxton, G.D. 2005. Warning displays in spiny animals: one (more) evolutionary route to aposematism. Evolution 59: 2499-2508.
   Google Scholar
• Stamp, N.E., Wilkens, R.T. 1993. On the cryptic side of life: being unapparent to enemies and the consequences for foraging and growth caterpillars. In: Stamp, N.E., Casey, T.M., eds. Caterpillars: ecological and evolutionary constraints on foraging. Chapman & Hall, New York, pp. 283-330.
   Google Scholar
• Stevens, M., Cuthill, I.C., Windsor, A.M.M., Walker, H.J. 2006. Disruptive contrast in animal camouflage. Proc. R. Soc. Lond. B 273: 2433-2438.
   Google Scholar
• Stone, B.C. 1979. Protective coloration of young leaves in certain Malaysian palms. Biotropica 11: 126.
   Google Scholar
• Stoner, C.J., Bininda-Emonds, O.R.P., Caro, T. 2003a. The adaptive significance of coloration in lagomorphs. Biol. J. Linn. Soc. 79: 309-328.
   Google Scholar
• Stoner, C.J., Caro, T.M., Graham, C.M. 2003b. Ecological and behavioral correlates of coloration in artiodactyls: systematic analyses of conventional hypotheses. Behav. Ecol. 14: 823-840.
   Google Scholar
• Thurston, E.L., Lersten, N.R. 1969. The morphology and toxicology of plant stinging hairs. Bot. Rev. 35: 393-412.
   Google Scholar
• Ungar, P.S., Teaford, M.F., Glander, K.E., Pastor, R.F. 1995. Dust accumulation in the canopy: a potential cause of dental microwear in primates. Am. J. Phys. Anthropol. 97: 93-99.
   Google Scholar
• Van Bael, S.A., Brawn, J.D., Robinson, S.K. 2003. Birds defend trees from herbivores in a Neotropical forest canopy. Proc. Natl. Acad. Sci. USA 100: 8304-8307.
   Google Scholar
• Waisel, Y. 1972. Biology of halophytes. Academic Press, New York.
   Google Scholar
• Waisel, Y., Litav, M., Agami, M. 1975. Coastal plants of Israel. Division of Ecology, Department of Botany, Tel Aviv University, Petah Tiqva (in Hebrew), 96 pp.
   Google Scholar
• Walker, A., Hoeck, H.N., Perez, L. 1978. Microwear of mammalian teeth as an indicator of diet. Science 201: 908-910.
   Google Scholar
• Werker, E. 2000. Trichome diversity and development. Adv. Bot. Res. 31: 1-35.
   Google Scholar
• Wiens, D. 1978. Mimicry in plants. Evol. Biol. 11: 365-403.
   Google Scholar