Herbivore adaptations to plant defense

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Herbivores are dependent on plants for food, and have coevolved mechanisms to obtain this food despite the evolution of a diverse arsenal of plant defenses against herbivory. Herbivores adaptations to plant defense have been likened to “offensive traits” and consist of those traits that allow for increased feeding and use of a host.[1] Plants, on the other hand, protect their resources for use in growth and reproduction, by limiting the ability of herbivores to eat them. Relationships between herbivores and their host plants often results in reciprocal evolutionary change. When an herbivore eats a plant it selects for plants that can mount a defensive response, whether the response is incorporated biochemically or physically, or induced as a counterattack. In cases where this relationship demonstrates “specificity” (the evolution of each trait is due to the other), and “reciprocity” (both traits must evolve), the species are thought to have coevolved.[2] The escape and radiation mechanisms for coevolution, presents the idea that adaptations in herbivores and their host plants, has been the driving force behind speciation.[3][4]

Contents

[edit] Mechanical adaptations

The molars of three species of elephant illustrate their different feeding preferences (l-asian elephant, c-african elephant, r-Mastodon ginganteum, all 1/4 size).
The molars of three species of elephant illustrate their different feeding preferences (l-asian elephant, c-african elephant, r-Mastodon ginganteum, all 1/4 size).

Herbivores have developed a diverse range of physical structures to facilitate the consumption of plant material. To break up intact plant tissues, mammals have developed teeth structures that reflect their feeding preferences. For instance, frugivores (animals that feed primarily on fruit) and herbivores that feed on soft foliage have low-crowned teeth specialized for grinding foliage and seeds. Grazing animals that tend to eat hard, silica-rich grasses, have high-crowned teeth, which are capable of grinding tough plant tissues and do not wear down as quickly as low-crowned teeth.[5] Birds grind plant material or crush seeds using their beaks.

Insect herbivores have evolved a wide range of tools to facilitate feeding. Often these tools reflect an individual’s feeding strategy and its preferred food type.[6] Within the family Sphingidae (e.g. moths), it has been observed that species whom eat relatively soft leaves are equipped with incisors for tearing and chewing, while the species that feed on mature leaves and grasses cut them with toothless snipping mandibles (the uppermost pair of jaws in insects, used for feeding).[7]

An herbivore’s diet often shapes its feeding adaptations. Grasshopper head size, and thus chewing power, was demonstrated to be greater for individuals raised on rye grass (a relatively hard grass) when compared to individuals raised on red clover (a soft diet).[8] Larval lepidoptera that feed on plants with high levels of condensed tannins (as in trees) have more alkaline midguts when compared to lepidoptera that feed on herbs and forbs (pH of 8.67 vs. 8.29 respectively). This morphological difference can be explained by the fact that insoluble tannin-protein complexes can be broken down and absorbed as nutrients at alkaline pH levels.[9]

[edit] Biochemical adaptations

Herbivores generate enzymes that counter and reduce the effectiveness of numerous toxic secondary metabolic products produced by plants. One such enzyme group, mixed function oxidases (MFOs), detoxify harmful plant compounds by catalyzing oxidative reactions.[10] Cytochrome P450 oxidases (or P-450), a specific class of MFO, have been specifically connected to detoxification of plant secondary metabolic products. One group linked herbivore feeding on plant material protected by chemical defenses with P-450 detoxification in larval tobacco hornworms.[11] The induction of P-450 after initial nicotine ingestion allowed the larval tobacco hornworms to increase feeding on the toxic plant tissues.[11]

Herbivores may also produce salivary enzymes that reduce the degree of defense generated by a host plant. The enzyme glucose oxidase, a component of saliva for the caterpillar Helicoverpa zea, counteracts the production of induced defenses in tobacco.[12] Similarly, aphid saliva reduces its host’s induced response by forming a barrier between the aphid’s stylet and the plant cells.[13]

[edit] Behavioral adaptations

Herbivores can avoid plant defenses by eating plants selectively in space and time. For the winter moth, feeding on oak leaves early in the season maximized the amount of protein and nutrients available to the moth, while minimizing the amount of tannins produced by the tree.[14] Herbivores can also spatially avoid plant defenses. The piercing mouthparts of species in Hemiptera allow them to feed around areas of high toxin concentration. Several species of caterpillar feed on maple leaves by "window feeding" on pieces of leaf and avoiding the tough areas, or those with a high lignin concentration.[15] Similarly, the cotton leaf perforator selectively avoids eating the epidermis and pigment glands of their hosts, which contain defensive terpenoid aldehydes.[1]

Plant defense may explain, in part, why herbivores employ different life history strategies. Monophagous species (animals that eat plants from a single genus) must produce specialized enzymes to detoxify their food, or develop specialized structures to deal with sequestered chemicals. Polyphagous species (animals that eat plants from many different families), on the other hand, produce more detoxyfying enzymes (specifically MFO) to deal with a range of plant chemical defenses.[16] Polyphagy often develops when an herbivore’s host plants are rare as a necessity to gain enough food. Monophagy is favored when there is interspecific competition for food, where specialization often increases a animals’ competitive ability to use a resource.[17]

[edit] Microbial symbionts

Herbivores are unable to digest complex cellulose and rely on mutualistic, internal symbiotic bacteria, fungi, or protozoa to break down cellulose so it can be used by the herbivore. Microbial symbionts also allow herbivores to eat plants that would otherwise be inedible by detoxifying plant secondary metabolites. For example, fungal symbionts of cigarette beetles use certain plant allelochemicals as their source of carbon, in addition to producing detoxification enzymes (esterases) to get rid of other toxins.[18] Microbial symbionts also assist in the acquisition of plant material by weakening a host plant’s defenses. Some herbivores are more successful at feeding on damaged hosts.[1] As an example, several species of bark beetle introduce blue stain fungi of the genera Ceratocystis and Ophiostoma into trees before feeding.[19] The blue stain fungi cause lesions that reduce the trees’ defensive mechanisms and allow the bark beetles to feed.[20][21]

[edit] Host manipulation

Galls (upper left and right) formed on the branch of an English Oak tree by the parthenogenetic gall wasp Andricus quercuscalicis.
Galls (upper left and right) formed on the branch of an English Oak tree by the parthenogenetic gall wasp Andricus quercuscalicis.

Herbivores often manipulate their host plants to use them better as resources. Herbivorous insects favorably alter the microhabitat in which the herbivore feeds to counter existing plant defenses. For example, caterpillars from the families Pyralidae and Ctenuchidae roll mature leaves of the neotropical shrub Psychotria horizontalis around an expanding bud that they consume. By rolling the leaves, the insects reduce the amount of light reaching the bud by 95%, and this shading prevents leaf toughness and leaf tannin concentrations in the expanding bud, while maintaining the amount of nutritional gain of nitrogen.[22] lepidoptera larvae also tie leaves together and feed on the inside of the leaves to decrease the effectiveness of the phototoxin hypericin in St. John’s-wort.[23]

Herbivores also manipulate their microhabitat by forming galls, plant structures comprised of plant tissue but controlled by the herbivore. Galls act as both domatia (housing), and food sources for the gall maker. The interior of a gall is composed of edible nutritious tissue. Aphid galls in narrow leaf cottonwood (Populus angustifolia) act as “physiologic sinks,” concentrating resources in the gall from the surrounding plant parts.[24] Galls may also provide the herbivore protection from predators.[25]

Some herbivores use feeding behaviors that are capable of disarming the defenses of their host plants. One such plant defensive strategy is the use of latex and resin canals that contain sticky toxins and digestibility reducers. These canal systems store fluids under pressure, and when ruptured (i.e. from herbivory) secondary metabolic products flow to the release point.[26] Herbivores can evade this defense, however, by damaging the leaf veins. This technique minimizes the outflow of latex or resin beyond the cut and allows herbivores to freely feed above the damaged section. Several strategies are employed by herbivores to relieve canal pressure, including vein cutting and trenching. The technique used by the herbivore corresponds to the architecture of the canal system.[27] Dussourd and Denno examined the behavior of 33 species of insect herbivores on 10 families of plants with canals and found that herbivores on plants with branching canal systems used vein cutting, while herbivores found on plants with net-like canal systems employed trenching to evade plant defenses.[27]

[edit] Herbivore use of plant chemicals

Plant chemical defenses can be used by herbivores, by storing eaten plant chemicals, and using them in defense against predators.

The bright colors of this Yellow-winged Darter dragonfly serve as a warning to predators of its noxious taste.
The bright colors of this Yellow-winged Darter dragonfly serve as a warning to predators of its noxious taste.

To be effective defensive agents, the sequestered chemicals cannot be metabolized into inactive products. Using plant chemicals can be costly to herbivores because it often requires specialized handling, storage, and modification.[28] This cost can be seen when plants that use chemical defenses are compared to those plants that do not, in situations when herbivores are excluded. Caterpillar and adult monarch butterflies store cardiac glycosides from milkweed, making these organisms distasteful. After eating a monarch caterpillar or butterfly, the bird predator will usually vomit, leading the bird to avoid eating similar looking butterflies in the future.[29] Two different species of milkweed bug in the family Hemiptera, Lygaeus kalmii and Oncopeltus fasciatus, are colored with bright orange and black, and are said to be aposematically colored, in that they “advertise” their distastefulness by being brightly colored.[30]

Secondary metabolic products can also be useful to herbivores due to the antibiotic properties of the toxins, which can protect herbivores against pathogens.[31] Additionally, secondary metabolic products can act as cues to identify a plant for feeding or oviposition (egg laying) by herbivores.

[edit] See also

[edit] References

  1. ^ a b c Karban, R., and A. A. Agrawal. 2002. Herbivore offense. Annual Review of Ecology and Systematics 33:641 – 664.
  2. ^ Futuyma, D. J. and M. Slatkin. 1983. Introduction. Pages 1−13 in D. J. Futuyma and M. Slatkin, editors. Coevolution. Sinauer Associates Inc., Sunderland, Massachusetts, USA.
  3. ^ Ehrlich, P. R. and P. H. Raven. 1964. Butterflies and plants: a study of coevolution. Evolution 18:586-608.
  4. ^ Thompson, J. 1999. What we know and do not know about coevolution: insect herbivores and plants as a test case. Pages 7–30 in H. Olff, V. K. Brown, R. H. Drent, and British Ecological Society Symposium 1997 (Corporate Author), editors. Herbivores: between plants and predators. Blackwell Science, London, UK.
  5. ^ Romer, A. S. 1959. The vertebrate story. University of Chicago Press, Chicago, USA.
  6. ^ Bernays, E. A. 1991. Evolution of insect morphology in relation to plants. Philosophical Transactions Royal Society of London Series B. 333:257 – 264.
  7. ^ Bernays, E. A., and D. H. Janzen. 1988. Saturniid and sphingid caterpillars: two mays to eat leaves. Ecology 69:1153 – 1160.
  8. ^ Thompson, D. B. 1992. Consumption rates and the evolution of diet-induced plasticity in the head morphology of Melanoplus femurrubrum (Othoptera: Acrididae). Oecologia 89:204 – 213.
  9. ^ Berenbaum, M. 1980. Adaptive significance of midgut pH in larval lepidoptera. The American Naturalist 115:138 – 146.
  10. ^ Feyereisen, R. 1999. Insect P450 enzymes. Annual Review of Entomology 44:507 – 533.
  11. ^ a b Snyder, M. J., and J. I. Glendinning. 1996. Causal connection between detoxification enzyme activity and consumption of a toxic plant compound. Journal of Comparative Physiology A 179:255 – 261.
  12. ^ Musser, R. O., S. M. Hum-Musser, H. Eichenseer, M. Peiffer, G. Ervin, J. B. Murphy, and G. W. Felton. 2002. Herbivory: caterpillar saliva beats plant defense – A new weapon emerges in the evolutionary arms race between plants and herbivores. Nature 416:599 – 600.
  13. ^ Felton, G. W., and H. Eichenseer. 1999. Herbivore saliva and its effect on plant defense against herbivores and pathogens. Pages 19 – 36 in A. A. Agrawal, S. Tuzun, and E. Bent, editors. Induced plant defenses against pathogens and herbivores. American Phytopathologial Society, St. Paul, Minnesota, USA.
  14. ^ Feeny, P. P. 1970. Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51:565 – 581.
  15. ^ Hagen, R. H., and J. F. Chabot. 1986. Leaf anatomy of maples (Acer) and host use by Lepidoptera larvae. Oikos 47:335 – 345.
  16. ^ Krieger, R. I., P. P. Feeny, and C. F. Wilkinson. 1971. Detoxication enzymes in the guts of caterpillars: An evolutionary answer to plant defenses? Science 172:579 – 581.
  17. ^ Jaenike, J. 1990. Host specialization in phytophagous insects. Annual Review of Ecology and Systematics 21:243 – 273.
  18. ^ Dowd, P. 1991. Symbiont-mediated detoxification in insect herbivores. Pages 411 – 440 in P. Barbosa, V. A. Krischik, and C. Jones, editors. Microbial mediation of plant – herbivore interactions. Wiley & Sons, Inc., New York, USA.
  19. ^ Krokene, P., and H. Solheim. 1998. Pathogenicity of four blue-stain fungi associated with aggressive and nonaggressive bark beetles. Phytopathology 88:39 – 44.
  20. ^ Whitney, H. S. 1982. Relationships between bark beetles and symbiotic organisms. Pages 183 – 211 in J. B. Mitton and K. B. Sturgeon, editors. Bark beetles in North American conifers. University of Texas Press, Austin, Texas, USA.
  21. ^ Nebeker, T. E., J. D. Hodges, and C. A. Blanche. 1993. Host response to bark beetle and pathogen colonization. Pages 157 – 173 in T. Schowalter, editor. Beetle-pathogen interactions in conifer forests. Academic Press, New York, USA.
  22. ^ Sagers, C. L. 1992. Manipulation of host plant quality: Herbivores keep leaves in the dark. Functional Ecology 6:741 – 743.
  23. ^ Sandberg, S. L., and M. R. Berenbaum. 1989. Leaf-tying by tortricid larvae as an adaptation for feeding on phototoxic Hypericum perforatum. Journal of Chemical Ecology 15:875 – 885.
  24. ^ Larson, K. C., and T. G. Whitham. 1991. Mapulation of food resources by a gall-forming aphid: the physiology of sink-source interactions. Oecologia 88:15 – 21.
  25. ^ Weis, A. E., and A. Kapelinski. 1994. Variable selection on Eurosta’s gall size. II. A path analysis of the ecological factors behind selection. Evolution 48:734 – 745.
  26. ^ Dussourd, D. E., and R. F. Denno. 1994. Host range of generalist caterpillars: Trenching permits feeding on plants with secretory canals. Ecology 75:69 – 78.
  27. ^ a b Dussourd, D. E., and R. F. Denno. 1991. Deactivation of plant defense: correspondence between insect behavior and secretory canal architecture. Ecology 72:1383 – 1396.
  28. ^ Bowers, M. D. 1992. The evolution of unpalatablility and the costs of chemical defense in insects. Pages 216 – 244 in B. D. Roitberg and M. B. Isman, editors. Insect chemical ecology. Chapman and Hall, New York, USA.
  29. ^ Huheey, J. E. 1984. Warning coloration and mimicry. Pages 257 – 300 in W. J. Bell and R. T. Carde, editors. Chemical ecology of insects. Chapman and Hall, New York, USA.
  30. ^ Guilford, T. 1990. The evolution of aposematism. Pages 23 – 61 in D. L. Evans and J. O. Schmidt, editors. Insect defenses: Adaptive mechanisms and strategies of prey and predators. State University of New York Press, Albany, New York, USA.
  31. ^ Frings, H., E. Goldberg, and J. C. Arentzen. 1948. Antibacterial action of the blood of the large milkweed bug. Science 108:689 – 690.
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