POPULATION GROWTH 9.6 TO 9.10 Birthrate and survivorship determine NetReproductive Rate
The fecundity table uses the survivorship column, l x , from the
life table together with the age-specifi c birthrates ( b x ) described earlier. Although b x may initially increase with age, survivorship ( l x ) in each age class declines. To adjust for mortality, we multiply the b x values by the corresponding l x , the survivorship values. The resulting value, l x b x , gives the mean number of females born in each age group, adjusted for survivorship. Age-specific Mortality and birthrates can be used to project population growth Age-specificmortality rates ( q x ) from the life table together with the age-specific birthrates ( b x ) from the fecundity table can be combined to project changes in the population into thefuture. The year of establishment is designated as year 0. The introduced population of female squirrels consists of 20 juveniles (age 0) and 10 adults (age 1), giving a total population of N (0) 30. The following table gives age-specific birthrates ( b x ), survival rates ( s x ), and number of females in each age class ( x ) at year 0. These values can now be used to project the population at year 1. Note that by substituting N (0) for N (1) (see above), we can rewrite the equation predicting N (2) as
In fact, we can use to project the population at any year
into the future using the following general form of the relationship developed previously: The geometric and exponential models developed thus far provide an important theoretical framework for understanding the demographic processes governing the dynamics of populations. But nature is not constant; systematic and stochastic (random) processes, both internal (demographic) and external (environmental), can infl uence population dynamics. Stochastic process scan influence population dynamics The realization that population dynamics represent the combined outcome of many individual probabilities has led to the development of probabilistic, or stochastic models of population growth. These models allow the rates of birth and death to vary about the mean estimate represented by the values of b x and s x . The stochastic (or random) variations in birth and death rates occurring in populations from year to year are called demographic stochasticity, and they cause populations to deviate from the predictions of population growth based on the deterministic models discussed in this chapter. Besides demographic stochasticity, random variations in the environment, such as annual variations in climate (temperature and precipitation) or the occurrence of natural disasters such as fi re, fl ood, and drought, can directly infl uence birth and death rates within the population. Such variation is referred to as environmental stochasticity. A variety of factors can lead to population extinction Extreme environmental events, such as droughts, fl oods, or extreme temperature events (heat or cold), can increase mortality rates and reduce population size. Should the environmental conditions exceed the bounds of tolerance for the species, the event could well lead to extinction. Small population are susceptable to extinction Small populations can be susceptible to a variety of factors that directly infl uence the rates of survival and birth. Small populations are more susceptible to both demographic and environmental stochasticity. If only a few individuals make up the population, the fate of each individual can be crucial to the survival of the population. Declining population size also may directly infl uence birthrates as a result of life history characteristics related to mating and reproduction .