A secondary consumer is a step above the primary consumer (herbivore) on the food chain, consisting of omnivores and carnivores. A mouse that lives off plant matter and is thus a primary consumer. When a snake eats the mouse, it is the secondary consumer in the food web.

With every advancement in the trophic level, energy converts on a ten-to-one scale. For example, ten kilograms of grain fed to a steer produces roughly one kilogram of beef. This is true for every step up the tropic food pyramid.

These are all sources of lost energy in between levels of the trophic pyramid. In the context of herbivores and carnivores: Not all food at each level can be eaten, because some prey escape their predators or they can't be found. When a predator eats its prey, not all of that tissue is digestible, such as cellulose and lignins. Lastly, everything that the predator digests is not used for new growth, and some is lost through excretion and respiration (heat).

Herbivores are very likely limited by the predators in their own food webs, preventing them from completely overtaking the plants that they feed on. This is called the Earth is Green hypothesis, originally proposed by Hairston, Smith, and Slodobkin.

Detritivores are successful because it is much more efficient to digest dung because it doesn't require much extra digesting, as another animal has already done it. Detritivores can generally have a much less complicated digestive system and save themselves the energetically expensive process of digesting new plants or animals. Detritivores are also important to the ecosystem because they cycle the nutrients in dung back into the food chain. There is no evidence that detritivores experience less competition, nor that detritus is in excess to live organisms.

Less than half of total solar energy is within the photosynthetically active wavelength range, and plants to not absorb all of this energy due to reflection and refraction. Thus, only about 1-5% of incoming solar radiation is actually converted to plant biomass, which serves as the base for all food chains. This is why herbivorous animals generally have to eat extremely high quantities of plants to achieve adequate nutrition.

Eusociality is defined by options I, II, and III. A species must cooperate on brood care (think ants bringing food back to the colony), labor is divided by reproductive ability (think sterile worker bees and queens) and the generations must overlap so that the colony is maintained properly.

Species designated as K-strategists thrive through longevity and have a higher survival rate at birth, but produce far fewer offspring. Examples include elephants and whales. Consider an elephant; it may produce relatively few baby elephants, but these baby elephants each have the potential to live relatively long lives. On the other hand, contrast K-strategists like elephants with r-strategists like rats, locusts, and flies. These species are designated as r-strategists because in contrast, they produce numerous offspring, few of which may survive to adulthood, and each one of which reaches maturity quickly and lives a relatively short life. K-strategists in general spend more time than r-strategists caring for and raising their offspring; they have fewer offspring, so they put more care into ensuring the survival of each one. Contrast elephants with frogs to see this difference; elephants care for their young, while frogs lay their eggs and care for their offspring very little, if at all.

Species described as "r-strategist" have a survival strategy of producing large numbers of offspring, a short life expectancy, and typically smaller body sizes. Examples include mice, locusts, and frogs. These species survive by producing lots of offspring, since many individuals don't survive to adulthood.

K-strategist populations are more commonly regulated by density-dependent limiting factors. Their population sizes hover around a carrying capacity that is dependent on factors that increase in severity with the density of the population. On the other hand, r-strategist populations are regulated by density-independent limiting factors. They reproduce rapidly until a density-independent factor causes many of them to die.