Defence against herbivory
Many plants produce chemicals which change the behaviour, growth, or survival of herbivores. These chemical defences can act as repellents or toxins to herbivores, or reduce plant digestibility. Some plants encourage the presence of natural enemies of herbivores, which in turn protect the plant.
Other defensive strategies used by plants include escaping or avoiding herbivores in time or in place. They may grow where plants are not easily found or got at by herbivores. They may grow when herbivores are not around. Herbivores may get diverted towards non-essential parts, or a plant may be able to recover from the damage caused by herbivory.
Each type of defence can be either constitutive (always present in the plant), or induced (produced in reaction to damage or stress caused by herbivores). Plants can and do react to damage.
Historically, insects have been the most significant herbivores, and the evolution of land plants is closely associated with the evolution of insects. While most plant defences are directed against insects, other defences have evolved that are aimed at vertebrate herbivores, such as birds and mammals.
The study of plant defences against herbivory is important, not only from an evolutionary viewpoint, but also because these defences can be used in agriculture, including human and livestock food sources.
Plant chemicals have evolved to affect insects. Some of these biochemical pathways exist in vertebrates, including humans. Many pharmaceuticals are got from the chemicals plants use to protect themselves from herbivores. Examples are opium, aspirin, cocaine, and atropine.
Evolution of defensive traits[change | change source]
The earliest land plants evolved from aquatic plants around 450 million years ago (mya) in the Ordovician period. These early land plants had no vascular tissue and needed free water for their reproduction. Vascular plants appeared later and their diversification began in the Devonian era (about 400 mya). They had adaptations such as protective coatings to reduce evaporation from their tissues.
Reproduction and dispersal of vascular plants in these dry conditions was achieved through the evolution of specialized seed structures. The diversification of flowering plants (angiosperms) during the Cretaceous period is associated with the sudden burst of speciation in insects. This diversification of insects represented a major selective force in plant evolution, and led to selection of plants that had defensive adaptations. Early insect herbivores bit or chewed vegetation; but the evolution of vascular plants lead to the co-evolution of other forms of herbivory, such as sap-sucking, leaf mining, gall forming and nectar-feeding.
Records of herbivores[change | change source]
Our understanding of herbivory in geological time comes from three sources:
- fossilized plants which may preserve evidence of defense (such as spines), or herbivory-related damage;
- the observation of plant debris in fossilised coprolite (animal faeces); and
- the construction of herbivore mouthparts.
Long thought to be a Mesozoic phenomenon, evidence for herbivory is found almost as soon as fossils which could show it. Within under 20 million years of the first fossils of sporangia and stems towards the close of the Silurian, around 420 mya, there is evidence that they were being eaten. Animals fed on the spores of early Devonian plants, and the Rhynie chert also provides evidence that organisms fed on plants using a "pierce and suck" technique. Many plants of this time are preserved with spine-like growths, which may have had a defensive role.
During the ensuing 75 million years, plants evolved a range of more complex organs – from roots to seeds. There was a gap of 50 to 100 million years between each organ evolving, and it being fed upon. Hole feeding and skeletonization are recorded in the early Permian, with surface fluid feeding evolving by the end of that period.
Co-evolution[change | change source]
Herbivores depend on plants for food, and have evolved mechanisms to get this food despite the evolution of many plant defences. Herbivore adaptations to plant defence have been likened to offensive traits. They are adaptations which allow increased feeding and use of a host plant. Relationships between herbivores and their host plants often results in reciprocal evolutionary change, called co-evolution.
When a herbivore eats, it eats plants that do not mount a sufficient defensive response. This creates the opportunity for plants which can mount a defence. So plants with defences become the more common. In cases where this relationship demonstrates specificity (the evolution of each trait is due to the other), and reciprocity (both traits evolve), the species are thought to have co-evolved.
The "escape and radiation" mechanism for co-evolution is the idea that adaptations in herbivores and their host plants have been the driving force behind speciation. The adaptations have played a role in the radiation of insect species during the age of angiosperms. Some herbivores have evolved ways to hijack plant defences to their own benefit, by sequestering (keeping) these chemicals and using them to protect themselves from predators.
Plants also need animals[change | change source]
Most of the plants which defend their leaves so vigorously nevertheless do need animals. Up to 98% of flowering plants in tropical lowland rain forests rely on animals for pollination and seed dispersal.
References[change | change source]
- Boyd, Jade 2012. A bit touchy: Plants' insect defenses activated by touch. Rice University. 
- Ghosh, B. (2000). "Polyamines and plant alkaloids". Indian Journal of Experimental Biology 38 (11): 1086–91. PMID 11395950.
- Ehrlich, Paul R.; Peter H. Raven (1964). "Butterflies and plants: a study of coevolution". Evolution (Society for the Study of Evolution) 18 (4): 586–608. doi:10.2307/2406212.
- Labandeira, C.C. et al (1994). "Ninety-seven million years of angiosperm-insect association: paleobiological insights into the meaning of coevolution" (PDF). Proceedings of the National Academy of Science of the United States of America 91 (25): 12278–82. doi:10.1073/pnas.91.25.12278. PMC 45420. PMID 11607501. http://www.pnas.org/cgi/reprint/91/25/12278.pdf.
- Labandeira C.C. (1998). "Early history of arthropod and vascular plant associations 1". Annual Reviews in Earth and Planetary Sciences 26 (1): 329–377. doi:10.1146/annurev.earth.26.1.329.
- Labandeira C. (2007). "The origin of herbivory on land: initial patterns of plant tissue consumption by arthropods". Insect Science 14: 259–275.
- Karban, Richard; Anurag A. Agrawal (2002). "Herbivore offense". Annual Review of Ecology and Systematics 33 (1): 641–664. doi:10.1146/annurev.ecolsys.33.010802.150443.
- Futuyma, Douglas J. & Slatkin, Montgomery (1983). Coevolution. Sunderland, Massachusetts: Sinauer. ISBN 0-87893-228-3.
- Thompson, J. (1999). "What we know and do not know about coevolution: insect herbivores and plants as a test case". In H. Olff, V.K. Brown, R.H. Drent. Herbivores: between plants and predators; the 38th symposium of the British Ecological Society. Oxford: Blackwell Science. pp. 7–30. ISBN 0-632-05155-8.
- Farrell, Brian D.; Charles Mitter (1994). "Adaptive radiation in insects and plants: time and opportunity". American Zoologist 34 (1): 57–69. doi:10.1093/icb/34.1.57.
- Bawa K.S. 1990. Plant pollinator interactions in tropical rain forests. Annual Review of Ecology and Systematics. 21, 167–196.
Further reading[change | change source]
- Bakker, Robert T. 1986. The dinosaur heresies: new theories unlocking the mystery of the dinosaurs and their extinction. Morrow. Chapter 8: Dinosaurs at table. ISBN 0-8065-2260-7
- Strong D.R., Lawton J.W. and Southwood, Sir Richard 1984. Insects on plants: community patterns and mechanisms. Blackwell, Oxford. Chapter 6 Coevolution.ISBN 0-632-00909-8