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Vertebrate predators

In contrast to the controlled use of these compounds in the neighborhood of farms and human habitation, they have sometimes been used in a less controlled way against rodents and vertebrate predators, which causes problems in conserved areas. In a number of conserved islands in New Zealand, for example, bait containing brodiphacoum has been used for rodent control, both at bait stations and by aerial distribution (Eason et al. 2002). In the latter case, poisoned bait is freely available, and herbivores and omnivores, as well as predators and scavengers are at high risk. This problem will be discussed further in Section 11.6. [Pg.223]

When ARs have been used to control rodents and vertebrate predators in conserved areas, there have been instances of both primary and secondary poisoning. In New Zealand, such incidents have been observed on islands where bait treated with brodifacoum has been used. Casualties have included native raptors, such as the Australasian harrier (Circus approximans) and morepork (Ninox novaeseelaniae), as well as other species, such as the pukeko. Western weka (Galliralus australis), and... [Pg.226]

Machado, G. et al.. Chemical defense in harvestmen (Arachnida, Opiliones) do benzoquinone secretions deter invertebrate and vertebrate predators J. Chem. EcoL, 31, 2519, 2005. [Pg.119]

Invertebrate allomones that deter vertebrate predators 10.7.1 Taste aversion to invertebrate prey... [Pg.264]

Table 10.3 lists some defense compounds, mostly alkaloid, that invertebrates use to deter vertebrate predators. [Pg.265]

Table 10.3 Allomones invertebrate compounds that deter vertebrate predators... Table 10.3 Allomones invertebrate compounds that deter vertebrate predators...
Vertebrate predator Invertebrate prey Compound(s) Reference... [Pg.266]

The presence of pyrrolizidine alkaloids in arctiid moths that had been reared on Senecio and Crotalaria species has been established by Rothschild et al.4S These alkaloids are stored in the moths, and serve as a deterrent to vertebrate predators and as precursors for insect sex pheromones. A pyrrolizidine alkaloid metabolite from the Cinnabar moth (Tyria jacobaea L.), named callimorphine, has been shown to have the structure (49) on the basis of mass-spectral and degradative evidence.46 The structure (49) was confirmed by synthesis of callimorphine and a diastereo-isomer by treatment of 9-chlororetronecine with the sodium salt of ( )-2-acetoxy-2-methylbutanoic acid. [Pg.65]

Retinoids are essential to fish and other vertebrates. Predators acquire them in the diet, either as retinol or retinyl esters they may also be acquired through the conversion of dietary carotenoids produced by plants (Fig. 2). In fish, carotenoids may be metabolized to retinol (vitamin Aj) or didehydroretinol (vitamin A2) (Fig. 1). For example, fish can convert canthaxanthin to /3-carotene47, which is a dimer of retinal that is readily converted to retinol (Figs. 1 and 2). Didehydroretinol (Fig. 1) is formed... [Pg.414]

Empirical data for vertebrate predators or even higher microbial forms of life display rather a Holling III type sigmoidal shape (Fig. 3.5) that can be modelled with the function... [Pg.115]

The cinnabar moth (Callimorphajacobaea L.) is unacceptable to a wide variety of vertebrate predators. The larvae feed on Senecio vulgaris L. and 8. jacobaea L. and the pupae in general have a higher concentration of total alkaloids than the plants upon which they have been reared. In both pupae and images there was detected a metabolite, Ci5H2505N, which was not present in the plants. Whether or not these alkaloids and the metabolites confer security from predators is not yet certain (179). [Pg.500]

Cortexone and 12-hydroxy-4,6-pregnadien-3,20-dione are feeding deterrents of certain water beetles (E 5.1). They act as hormones in vertebrate predators. [Pg.242]

Comparison of the pheromone systems of closely related species, has revealed that the attraction and the pheromone-receptor interaction found between them correlates with the degree of relatedness (Lanier and Wood, 1975 Priesner, 1979a, b). However, such a cross attraction could be disadvantageous for related species living in the same area, and under such circumstances an additional interspecific mechanism - interruption - is found which serves to maintain the isolation between sympatric species (Birch, Chapter 12). Thus, one species may produce an additional pheromone compound which interrupts the attraction of the other species. Chemical compounds which function as pheromones may also serve as cues for predators, parasitoids and prey (Vincent, Chapter 8). In these cases the predator or parasites have developed capabilities for recognizing the pheromones of their prey or host insects. Predators may also produce the attractants of their prey (Weaver, 1978 Eberhard, 1977). Conversely, some insect species have developed defensive compounds which are avoided by both insect and vertebrate predators, (cf. Eisner, 1970 Blum, 1978 Huheey, Chapter 10). Finally, during... [Pg.37]

Some pyrrohzidine alkaloids stored for defence (Bemays et ah, 1977), are used to biosynthesise hormones (Nishida et ah, 1996), or are converted to other toxic substances (Brown, 1984). The monarch butterfly, Danaus piexip-pus, exploits cardiac glycosides for defence against vertebrate predators (Roeske et ah, 1975) and glucosinolates are also favoured by some insects for this type of defence (Aliabadi et ah, 2002 Aplin et ah, 1975 Muller et ah, 2001). [Pg.334]

The question might be asked whether the reaction to a toxic material In the food Is any more effective at altering food habits than the other possible mechanism of repellent action, a simple bad-taste effect. Two lines of evidence suggest an answer to this question. First, and most powerful. Is the evidence, discussed above from plant evolution. The plants have emphasized defenses that adversely effect the physiology of their vertebrate predators, they have not frequently used taste stimuli except as cues to toxic events. Second, Is an experiment (30) that directly compared the effectiveness of toxic and non-toxic materials at altering the feeding behavior of red-winged blackbirds. [Pg.156]


See other pages where Vertebrate predators is mentioned: [Pg.130]    [Pg.280]    [Pg.90]    [Pg.392]    [Pg.401]    [Pg.406]    [Pg.232]    [Pg.95]    [Pg.214]    [Pg.405]    [Pg.77]    [Pg.1000]    [Pg.637]    [Pg.346]    [Pg.40]    [Pg.433]    [Pg.501]    [Pg.513]    [Pg.158]    [Pg.174]    [Pg.17]   
See also in sourсe #XX -- [ Pg.501 ]




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