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Herbivore

Benzoic acid in the free state, or in the form of simple derivatives such as salts, esters, and amides, is widely distributed in nature. Gum benzoin (from styrax ben in) may contain as much as 20% benzoic acid in the free state or in combinations easily broken up by heating. Acaroid resin (from anthorrhoca haslilis) contains from 4.5 to 7%. Smaller amounts of the free acid are found in natural products including the scent glands of the beaver, the bark of the black cherry tree, cranberries, pmnes, ripe cloves, and oil of anise seed. Pern and Tolu balsams contain benzyl benzoate the latter contains free benzoic acid as well. The urine of herbivorous animals contains a small proportion of the glycine derivative of benzoic acid, hippuric acid [495-69-2] (CgH CONHCH2COOH). So-called natural benzoic acid is not known to be available as an item of commerce. [Pg.52]

Exposure to estrogenic compounds through diet will differ for herbivores and carnivores, the latter being most likely to encounter endogenous steroids in their prey. Efficient uptake of steroids in mammals is illustrated by the use of the contraceptive pill, but routes of absorption in invertebrates remain to be determined. The relationship between endocrine disruption and metabolic toxicity, with reduced reproductive viability a secondary consequence of metabolic disturbance, also merits further study in invertebrate species. [Pg.54]

Ruminants (functional) Cattle, sheep Grazing herbivore... [Pg.98]

Antelope, deer, camel, llama Selective herbivore... [Pg.98]

Food chain Very simple pathway of nutrient flow. Ex. Carnivore > herbivore > plant. [Pg.615]

FIGURE 1.2 The food pyramid. Photosynthetic organisms at the base capture light energy. Herbivores and carnivores derive their energy ultimately from these primary producers. [Pg.4]

Vitamin Bjg is not synthesized by animals or by plants. Only a few species of bacteria synthesize this complex substance. Carnivorous animals easily acquire sufficient amounts of Bjg from meat in their diet, but herbivorous creatures typically depend on intestinal bacteria to synthesize Bjg for them. This is sometimes not sufficient, and certain animals, including rabbits, occasionally eat their feces in order to accumulate the necessary quantities of Big. [Pg.599]

In a temperate forest ecosystem on Isle Royale, Michigan, ecologists found that it takes 762 pounds (346 kg) of plant food to support every 59 pounds (27 kg) of moose, and that 59 pounds of moose are required to support every one pound (0.45 kg) of wolf. The basic point is that massive amounts of energy do not flow from one trophic level to the next energy is lost at each stage of the food chain, so there are more plants than herbivores and more herbivores than carnivores. [Pg.182]

A cyclobutene ROCM sequence was also used in a synthesis of racemic sporochnol (410), a naturally occurring feeding deterrent toward herbivorous fish (Scheme 80) [170]. Exposing cyclobutene 406 (0.01 M in boiling 1,2-dichloroethane) in the presence of ethylene to second-generation catalyst C (8 mol%) led to 1,5-diene 407 in 73% yield, along with 9% of the homodimer derived from 407 by involving the less hindered double bond. Site-selective hy-... [Pg.346]

Hartmann T, Ober D (2000) Biosynthesis and Metabolism of Pyrrolizidine Alkaloids in Plants and Specialized Insect Herbivores. 209. 207-243 Haseley SR, Kamerling JP, Vliegenthart JFG (2002) Unravelling Carbohydrate Interactions with Biosensors Using Surface Plasmon Resonance (SPR) Detection. 218 93-114... [Pg.233]

Where CO2 in the free atmosphere has a 5 C value of-7%o, C3 and C4 plants are anticipated to have 5 C values of about -26.5%o and -12.5%o respectively (van der Merwe 1989) archaeological maize, however, typically averages -9.5%o(Schwarcz et al. 1985). The isotopic values of modern maize and C3 plant foods in Mesoamerica (Wright 1994 203-206), after correction for the Industrial Effect, average -9.6%o and -26.4%o respectively. Since herbivore collagen is typically enriched by +5%o relative to the diet (van der Merwe 1989), animals from this region with a pure C3 plant diet should... [Pg.26]

Figure 3.2. Average carbon isotopic ratios for all human, herbivore, carnivore, and omnivore bone samples from the European Holocene in the data base A Uncorrected ratios (Cu) B climate-corrected ratios (Cc). Only countries with more than 10 samples are included. For a description of the climatic correction procedure see text. [Pg.44]

It can be argued that the gut flora provides an additional trophic level in ruminants (Steinhour et al. 1982). This should result in a larger A N in ruminants than in non-ruminant herbivores. As many domesticated animals are ruminants this is a factor that has to be taken into account. Available 5 N data does not seem to show systematic differences between the categories ruminants and non-ruminants, although systematic species differences exist. [Pg.48]

What are the reported carbon and nitrogen effects in humans Not much data has been published regarding herbivore-human carbon shifts. We will discuss our data in a later section. [Pg.48]

Study, ancient Maya diet shows a A N of 4.5%o (humans-herbivores). The 8 N values for mixed-diet humans in Schoeninger et al. (1983) seem always somewhat too positive for their supposed food European agriculturalists are about 8-10%o. Also, Bocherens et al. (1991) and Lubell et al. (1994) give similar values (aroimd +9%o) for medieval French and Neolithic humans from Portugal, respectively. The 8 N values (+9.3 and 11.6%o) of two human (Neanderthal) samples (Fizet et al. 1995) are very similar to those of associated carnivores but are only slightly higher than those of Neolithic humans. [Pg.49]

Table 3.2 shows the 5 Cu and 5 Cc values of herbivores, omnivores, carnivores and humans. The (climate-corrected) trophic level effect between herbivores and carnivores is 0.90%o. Human values are closer to carnivore and omnivore values than to herbivore 5 Cc values. The human 5 Cc values are on average 0.66%o more positive than the herbivore 5 Cc values, a good estimate for a carnivore effect in humans (see section on trophic level effects, below). The average human 5 Cc value is -19.92 1.28%o,which would indicate that Holocene humans in Europe had a diet that consisted of C3 terrestrial foods, whieh is as might be expected. By looking at the humans separate from the total bone data set, we notice potential human food selection (Fig. 3.3) we can see a non-climatic pattern, which is much less uniform than in the total bone data set (Fig. 3.2b). Italy (6 Cc = -21.3%o) has a much more negative 8 Cc value than the Czech Republic (8 Cc =-18.7%o), Spain (8 Cc = -19.3%o) and Greece (-18.9%o but the 8 N of 9.0%odoes not indicate marine food), while the northern European coimtries are closer to a 5 Cc value of-20%o. What the actual causes are for this pattern in the human samples is not clear to better understand these variations it is best to consider, where possible, the 8 N values with the 8 Cc values. [Pg.54]

Tabic 3.2. A comparison of the average 5 Cj and 5 Cc values of human, herbivore, carnivore, and omnivore bone samples from the European Holocene. [Pg.54]


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Alkaloids and Herbivorous Vertebrates

Allomones II plant chemical defenses against herbivores

Anti-herbivore

Anti-herbivore defense

Carbohydrates herbivore diets

Coevolution, plants/herbivores

Cyanogenesis plant-herbivore interactions

Defense herbivore response

Effects of Secondary Metabolites on Digestion in Marine Herbivores

Feeding herbivorous reef fish

Fish herbivorous

Food-chain herbivorous

Generalist insect herbivores

Herbivore Attack by Small Predators

Herbivore behaviour

Herbivore chewing

Herbivore deterrents

Herbivore offense

Herbivore pressure

Herbivore repellent

Herbivore tolerance

Herbivore urine

Herbivore-induced plant volatiles

Herbivore-induced plant volatiles responses

Herbivore-induced plant volatiles specificity

Herbivores Subject

Herbivores carbon Isotope

Herbivores coevolution with plants

Herbivores diets

Herbivores feeding patterns

Herbivores fractionation

Herbivores generalists

Herbivores host selection

Herbivores specialists

Herbivores, defense against, polyphenol

Herbivores, specialized

Herbivores, volatile terpenes from

Herbivorous crabs

Herbivorous fishes stimulants

Herbivorous insects

Herbivorous vertebrates

Large Herbivore Attack

Lipids herbivore diets

Macroalgal-herbivore interactions, chemical

Macroalgal-herbivore interactions, chemical defenses

Macroalgal-herbivore interactions, chemical marine herbivores

Macroalgal-herbivore interactions, chemical mediation

Microbial digestion in ruminants and other herbivores

Mollusc herbivorous

Norman G. Bisset Alkaloid Chemistry and Feeding Specificity of Insect Herbivores

Pests herbivores

Phlorotannin herbivore interactions

Photosynthetic Pathway Impacts Herbivores

Plant herbivore interactions

Plant protection (chemical herbivores

Plant-herbivore

Plant-herbivore relationships

Plant-herbivore theory

Plant-herbivore-community

Plant-herbivore-community relationships

Plant-insect interaction Herbivore defense

Plants and Herbivores

Protection against herbivores

Repellents, herbivores, effectiveness

Resistance against herbivores

Seaweed herbivore interactions

Stress herbivore

Using Population-Level Variation in Herbivore Traits as an Analytical Tool

Vertebrate herbivores

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