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Abstract:
Life tables are used to describe and understand the population dynamics of a species. This
information is important in conservation studies (reintroduction of species), agriculture
(reduction of pest species), and human health (following epidemics). Using reintroduction of
a species as an example, life tables can indicate when a breeding population has been
established. This is a study on meaning & explanation of life table. It includes definition,
types, formation & example of life table.
Key Words:
Demographic Mortality Variables Cohort
Static Reproductive Interval Survival
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The life table is one way of summarizing key demographic variables, including age-specific
mortality, survivorship, and expectation of further life. Once these data are compiled, we can
use them to investigate demographic patterns and processes, such as differences in the
survival rate or life expectancy of different groups of organisms. When this information is
combined with fecundity data, life-tables can be used to estimate rates of population change
(e.g., r, , and Ro).
generally yields a static life table, with entries that are age-specific, even though the sample is
a composite, made up of individuals who started life at different times.
Most organisms have more complex life histories than found in the above example, and while
it is possible to follow a single cohort from birth to death, it often too costly or time-
consuming does so. Another, less accurate, method is the static, or vertical, life table. Rather
than following a single cohort, the static table compares population size from different
cohorts, across the entire range of ages, at a single point in time. Static tables make two
important assumptions: 1) the population has a stable age structure that is, the proportion of
individuals in each age class does not change from generation to generation, and 2) the
population size is, or nearly, stationary.
Static life tables can also be made from knowing, or estimating, age at death for individuals
from a population. This can be a useful technique for secretive large mammals (e.g., moose)
from temperate regions where it is difficult to sample the living members. Because the
highest mortality of large herbivores occurs during the winter, an early spring survey of
carcasses from starvation and predator kills can yield useful information in constructing a life
table.
Besides R0, the basic reproductive rate, several other population characteristics can be
determined from life tables. Some of the most common features are the cohort generation
time (Tc), life expectancy (ex), and the intrinsic growth rate (r).Cohort generation time is
quite easy to obtain from our first example, a semelparous annual life cycle (Tc= 1 year), but
generation time is less obvious for more complex life cycles. Generation time can be denied
as the average length of time between when an individual is born and the birth of its
offspring. Therefore, it can be calculated by summing all the lengths of time to offspring
production for the entire cohort divided by the total offspring produced by the survivors:
Life expectancy is a useful way of expressing the probability of living x number of years
beyond a given age. We usually encounter life expectancy in newspaper articles comparing
the mean length of life for individuals of various populations. However, this value is actually
the life expectancy at birth. One can also calculate the mean length of life beyond any given
age for the population. Life expectancy is a somewhat complicated calculation. Because lx is
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only the proportion surviving to the beginning of a particular age class, we must first
calculate the average proportion alive at that age (Lx):
Next, the total number of living individuals at age x and beyond (Tx) is:
Finally, the average amount of time yet to be lived by members surviving to a particular age
(ex) is:
The basic reproduction rate (R0) converts the initial population size to the new size one
generation later as:
If R0 remains constant from generation to generation, then we can also use it to predict
population size several generations in the future. To predict poplulation size at any future
time, it is more convenient to use a parameter that already takes generation time into account.
This term is r, the intrinsic rate of natural increase, and it can be calculated (or approximated
for complex life cycles) by the following equation:
Example:
The following table provides an example of an abridged life table:
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Table 7-1
Example of an Abridged Life Table
Column 1
Age interval, x to x+n: Age interval between exact ages for each row of the life table.
Column 2
nQx: The proportion of the population in each age interval that is alive at the
beginning of the interval and dead before reaching the end of the interval. The
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proportion is computed from the observed mortality rates of an actual population and
is used to derive the remaining columns of the life table.
Column 3
lx: The number of persons alive at the beginning of the age interval
Column 4
ndx: The number of persons dying during the age interval
Column 5
Lx: The total number of person-years in the stationary population for each age
interval. It can be viewed as the average population size between birthdays, taking
into account the distribution of deaths throughout the year.
Column 6
Tx: This column records the stationary population in the indicated age interval and all
subsequent intervals. It is the cumulative sum of the nLx values. It can be viewed as
the total number of person-years that would be lived for a particular age cohort if the
cohort were to progress through the remainder of the life table.
a. No migration
c. An increase by a constant number of births each year and decrease by the same
constant number of deaths each year
d. Stationary age structure size In each age group, the number of person-years lived is
always the same as that of the original life table cohort.
When a person dies or enters the next higher age interval, their place is immediately taken by
someone entering from the next lower age interval. The number of persons in the age interval
remains the same. The values in the Lx and Tx columns are based on the assumption that an
additional 100,000 persons are added to the table annually and are subject to the mortality
rates computed in the nQx column. The population is considered stationary because the total
population and the number of people in each age interval do not change.
Column 7
e: This column indicates the average remaining lifetime for a given age group.
Life tables are used to calculate survival rates. For population projections, 5-year survival
rates are computed. For estimates of net migration, 10-year survival rates are calculated.
Calculations of survival rates rely on two columns in the life table, Lx and Tx.
Using the abridged life table presented in Table 7-1, calculate 5-year survival rates as shown
in Equation 7-1.
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Equation 7-1
5-year Survival Rate
To calculate a rate to survive women ages 2529 into the next 5-year age cohort (3034), use
the following numbers from the Lx column in Table 7-1, as shown in the following example.
This process is repeated for most age groups; the first and last age groups are exceptions.
Slight modifications are required to survive these two groups into the next age group.
Equation 7-2 provides an example of survival rates for those in the first age interval, 04.
Note that the initial size of the first cohort is multiplied by 5 in the denominator. Why? There
is no earlier value for Lx for the denominator. The number 100,000 is multiplied by 5
because, hypothetically, 100,000 new born babies are added to the table each year for a 5-
year period.
Equation 7-2
surviving the youngest age cohort
For the last age cohort (7585+),use the Tx column to create a 5-year survival rate as shown
in Equation 7-3. The value of Tx represents the number of survivors in a particular age group
and all older age groups.
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Equation 7-3
surviving the oldest age cohort
So, we can calculate various population factors from life tables in such ways.
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References:
Edwards, R.D. and Tuljapurkar, S. (2005). Inequality in life spans and a new
perspective on mortality convergence across industrialized countries. Population and
Development Review 31(4): 645674.
Goldman, N. and Lord, G. (1986). A new look at entropy and the life table.
Demography 23(2): 275282.
Vaupel, J.W. (1986). How change in age-specific mortality affects life expectancy.
Population Studies 40(1): 147157.
Edwards, R.D. and Tuljapurkar, S. (2005). Inequality in life spans and a new
perspective on mortality convergence across industrialized countries. Population and
Development Review 31(4): 645674.
Wilmoth, J.R. and Horiuchi, S. (1999). Rectangularization revisited: Variability of
age at death with human populations. Demography 36(4): 475495.
Zhang, Z.; Vaupel, J. W. (2009). The age separating early deaths from late deaths.
Demographic Research, 20:29, 721-730.