Lecture 23: Predation

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Reading:  Economy of Nature, pp. 400-414.

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Predation

This is an interaction resulting in harm to one individual and benefit to another individual. Defined as consumption of one organism by another. Prey is alive when predator first attacks. Not all consumption is predation, for example decomposers and scavengers. In these cases, there is no interaction between consumer and "prey", and no harm to the "prey" occurs as a result of consumption..

 

Functional Classification

True predator: Kills prey immediately upon attack and often consumes all of prey.

Grazer: Attacks large numbers of prey and only removes a part of each prey individual which is rarely lethal.

Parasite: Consume only a part of the prey, but often are closely associated with the prey for long periods of time. In many cases the parasite lives inside the prey host.

Parasitoid: A special type of parasite, typically insects that lay eggs on or near prey. Prey are entirely consumed and eventually killed by the parasitoid. Prey are other insect species, result is always lethal to the prey.

Herbivore-Plant Interactions

Consequences of Herbivory

Removal of biomass

Interactive herbivory: normal predation, herbivore influences individual prey growth rate, and distribution (defoliation and fluid removal)

Non-interactive herbivory: individuals growth and distribution of the parent plants is not influenced by this predation, at least in the short term (seed predation)

Disease spread: incidental consequences of herbivory

Plants are not helpless prey despite being sessile (fixed in one location).

Defense Mechanisms of Plants

Physical Defenses

Hairs, spines, hooks

Tissue texture

Chemical Defenses

Secondary compounds

Chemicals not required for "primary" metabolism and not necessarily defensive adaptations

Toxins or other anti-herbivore substances

Temporal Defenses

Timing of critical life history events that are subject to herbivory

Types of plant secondary compounds (Ricklefs, 1993, pp 334-335, Table 18.2 also see Ricklefs, 1996, p 413, Table 18.2).

Class Number Distribution Physiological activity
NITROGEN COMPOUNDS    
Alkaloids 10,000+ Widely in angiosperms, expecially in root, leaf, and fruit Many toxic and bitter-tasting
Amines 100 Widely in angiosperms, often in flowers Many repellent-smelling, some hallucinogenic
Amino Acids (nonprotein) 400 Especially in seeds of legumes but relatively widespread Many toxic
Cyanogenic glycosides 30 Sporadic, especially in fruit and leaf Poisonous (as HCN)
Glucosinolates 75 Cruciferae and 10 other families Acrid and bitter
TERPENOIDS      
Monoterpenes 1000 Widely, in essential oils Pleasant-smellng
Sesquiterpene lactones 600 Mainly in Compositae, but increasingly found in other angiosperms Some bitter and toxic, also allergenic
Diterpenoids 1000 Widely, especially in latex and plant resins Some toxic
Saponins 500 In over 70 plant species Haemolyse blood cells
Limonoids 100 Mainly in Turaceae, Meliaceae, and Simaroubaceae Bitter tasting
Curcurbitacins 50 Mainly in Cucurbitacaeae Bitter tasting and toxic
Cardenolides 150 Especially common in Apocynaceae, Asclepiadaceae, and Scrophularaceae Toxic and bitter
Carotenoids 350 Universal in leaf, often in flower and fruit Colored
PHENOLICS      
Simple phenols 200 Universal in leaf, often in other tissues as well Antimicrobial
Flavonoids 1000 Universal in angiosperms, gymnosperms, and ferns Often colored
Quinones 500 Widely, especially in Rhamnaceae Colored
OTHER      
Polyacetylenes 650 Mainly in compositae and Umbelliferae Some toxic
Source: J. B. Harborne, Introduction to Ecological Biochemistry (2nd. ed.). Academic Press, New York (1982)

Examples of some secondary compounds

Cardenolides: cardiac glycosides (modified monosaccharides)

Alkaloids: morphine, caffeine, nicotine, cocaine, cocoa

(N containing ring compounds)

Monoterpenes: peppermint, catnip, cinnamon, cloves

Polyphenols: tannins (common in leaves and bark of many woody plants)

 

A clear defensive function has not been demonstrated for every compound in each of the classes but many examples are unequivocal. White clover, Trifolium repens, leaves release hydrogen cyanide (HCN) when the leaves are damaged by herbivores. Hydrogen cyanide is a potent, rapidly acting metabolic toxin which discourages continued herbivore consumption of the white clover leaves.

Qualitative (type) defenses are toxic chemicals that are produced and are effective in small quantities. For example, many of the alkaloids are very effective toxins that mimic or interfere with herbivore neurotransmitters.

Quantitative (amount) defenses are interference substances, digestion inhibitors or resins that make herbivory more difficult, or less beneficial to the herbivore. For example, tannins bind to proteins and make them indigestible (however, some tannins may be toxic in small quantities so it is possible for a given compound to be both a quantitative and a qualitative defense). Tannins and resins may account for as much as 60% of leaf dry weight.

Food selection by herbivores may be regulated more by toxins than by digestion inhibitors, but the time scale of response need not be the same for all effective defenses.

As a working hypothesis, we assume that secondary compounds functioning specifically as chemical defense substances are produced at some cost to a plant (cost in energy and nutrients that could have been used for other purposes). These substances are not simply waste products or incidental byproducts of primary metabolism.

General Predictions About Plant Chemical Defenses (after Krebs, 1994)

1. Defenses evolve in response to selection by predation, but defenses reduce growth rates and reproductive output rates.

2. Defenses will be allocated to the most valuable tissues at risk.

3. Defenses will be reduced when herbivores are absent and increased in response to attack.

4. Defenses are costly and cannot be maintained if plant is under environmental stress.

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