BISC 111/113:Lab 11: Population Growth 2: Difference between revisions

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=='''Population Growth and Interactions: Background'''==
=='''Population Growth and Interactions: Background'''==
'''Population Structure'''<br>
Today you will complete the final counts of your Tribolium populations. Your samples have been placed in the freezer for at least 48 hours prior to the lab. You can isolate the beetles/pupae by sifting some of the culture through the screen over the brown paper on your bench. Try to keep all the flour away from the computers. As you isolate the beetles, put them in a labeled petri dish. There are tools available on your lab bench to help with the counting.
A population is a group of individuals of the same species in a given area with the potential to interbreed. Each population has a <b>structure</b> that includes features such as density, spacing, and movement of individuals over time and space.<br>
 
Enter your data on the class spreadsheet.
 
Refer to your lab instructor for information about the oral presentations workshop next week. Sign up for a topic before leaving lab today.
 
 
== '''Population''' ==
 
A population is a group of individuals of the same species in a given area with the potential to interbreed.
 
The study of '''population dynamics''' examines the ways that populations grow or shrink over time. Reproduction and immigration account for population increases, and death and emigration account for decreases. The '''population growth rate''' is the change in the number of individuals in a population per unit time.  While some populations may reproduce continually, others experience discrete periods of reproductive growth. When a population (e.g. human) has no distinct reproductive season, the population grows more or less continuously While some populations may reproduce continually, others experience discrete periods of reproductive growth. When a population (e.g. human) has no distinct reproductive season, the population grows more or less continuously. <br><br>
 
Each population has a <b>structure</b> that includes features such as density, spacing, and movement of individuals over time and space. Analyzing patterns of population size, structure, and distribution is a fundamental conservation biology concept.<br>


<b>Spatial structure</b> addresses the dispersal of individuals in space and can be classified as evenly spaced, clumped or totally random. <b>Genetic structure</b> of a population describes the distribution of genetic variation within that group. There is genetic variation among individuals within the population. This variation is the basis of the population’s ability to respond to environmental changes through adaptive evolution.
<b>Spatial structure</b> addresses the dispersal of individuals in space and can be classified as evenly spaced, clumped or totally random. <b>Genetic structure</b> of a population describes the distribution of genetic variation within that group. There is genetic variation among individuals within the population. This variation is the basis of the population’s ability to respond to environmental changes through adaptive evolution.


The study of '''population dynamics''' examines the ways that populations grow or shrink over time. Reproduction and immigration account for population increases, and death and emigration account for decreases. While some populations may reproduce continually, others experience discrete periods of reproductive growth. Because some populations (e.g. human) have no distinct reproductive season, the population grows more or less continuously. <br><br>
'''Mathematical models''' offer a way to describe and predict population growth over time and under a variety of conditions. Generally, populations grow by multiplication, if all individuals have the potential to contribute equally to the population by reproducing. It follows that the amount of growth that occurs is proportional to population size. As an example, consider the measurements of a population’s size below. How fast is this population growing?


'''Geometric Growth'''<br>
  How fast is this population growing?<br>
Mathematical models offer a way to describe and predict population growth over time and under a variety of conditions.  Generally, populations grow by multiplication, if all individuals have the potential to contribute equally to the population by reproducing.  It follows then that the amount of growth that occurs is proportional to population size.  As an example, consider the measurements of a population’s size below. How fast is this population growing?<br>
<center>
<center>
{| border="1"  
{| border="1"  
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</blockquote>
</blockquote>


'''Exponential Growth'''<br>
We can use this expression to predict the population size at any future time “t” from some initial size (<b>N<sub>0</sub></b>), if the population growth rate (<b>λ</b>) is constant.  In our example above where N<sub>0</sub> = 100 individuals, after 15 years the population would be predicted to be quite large under a constant population growth rate of 1.6 (N<sub>15</sub> = 100 *  1.6<sup>15</sup> , or > 115 * 10<sup>3</sup> individuals).<br><br>


Calculations involving population growth can be more easily handled if we express the population growth rate as an <i>exponential constant</i>, <b>r</b>, rather than the geometric constant, <b>λ</b>.  We can do this by substituting <b>e<sup>r</sup></b>, for <b>λ</b> in our computations.  “<b>e</b>” is the base of Naperian, or natural,  logarithms, and is equal to approximately 2.718.  The equation for <i>exponential population growth</i> then, is<blockquote>
== '''Population regulation''' ==


<center><b>N<sub>t</sub> = N<sub>0</sub> * e<sup>rt</sup></b></center></blockquote>


Why use <b>r</b> instead of <b>λ</b>? The geometric constant depends on the interval of time specified; <b>λ</b>= 1.6 over 1 yr, in the previous example, but 2.56 over 2 yr.  The exponential constant <b>r</b> is an instantaneous measure of relative population growth at every moment in time, and is hence more generally useful.  Exponential growth is like a compound interest savings account, where the interest is continually added to the principal.  Geometric growth is akin to simple interest, where the account balance is updated once a year. Exponential growth is especially applicable to continuously reproducing populations, such as the human population.   
'''Density Independent growth'''
When the growth rate does not depend on the number of individuals in the population,  growth is density independent.  In density independent models birth and death rates remain constant no matter how many individuals are in the population, an unlikely occurrence in natural populations over a long period of time.
 
'''Density-independent factors,''' in particular, environmental factors such as temperature, precipitation, and disturbances (e.g., fire, floods, earthquakes, tsunamis) can alter the rate of population growth. These factors, however, are density independent because they affect a certain proportion of the population independently of population size (and largely independent of individual fitness).
 
 
'''Exponential Growth is a density independent model of population growth.'''
We can use exponential growth to predict the population size at any future time “t” from some initial size (N0), if the population growth rate (λ) is constant. In our example above where N0 = 100 individuals, after 15 years the population would be predicted to be quite large under a constant population growth rate of 1.6 (N15 = 100 * 1.615 , or  >115 * 103 individuals).
 
Calculations involving population growth can be more easily handled if we express the population growth rate as an exponential constant, r, rather than the geometric constant, λ. We can do this by substituting er, for λ in our computations. “e” is the base of Naperian, or natural, logarithms, and is equal to approximately 2.718. The equation for exponential population growth then, is
Nt = N0 * ert
 
Why use <b>r</b> instead of <b>λ?</b>  The geometric constant depends on the interval of time specified; <b>λ</b>= 1.6 over 1 yr, in the previous example, but 2.56 over 2 yr.  The exponential constant <b>r</b> is an instantaneous measure of relative population growth at every moment in time, and is hence more generally useful.  Exponential growth is like a compound interest savings account, where the interest is continually added to the principal.  Geometric growth is akin to simple interest, where the account balance is updated once a year. Exponential growth is especially applicable to continuously reproducing populations, such as the human population.   


During exponential growth, the population grows by an amount <b><i>d</i>N</b>, during a time interval <b><i>d</i>t</b> (this is the population growth rate) and the amount of growth in this interval is proportional to the size of the population (<b>N<sub>t</sub></b>) by the constant <b>r</b>:
During exponential growth, the population grows by an amount <b><i>d</i>N</b>, during a time interval <b><i>d</i>t</b> (this is the population growth rate) and the amount of growth in this interval is proportional to the size of the population (<b>N<sub>t</sub></b>) by the constant <b>r</b>:
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</blockquote>
</blockquote>


'''Linear Growth.''' <br>
Linear models may be appropriate over short time intervals, but seldom describe long-term population growth because they fail to include an increasing number of reproductive individuals as the population grows.  However, while exponential growth models are more realistic than the linear models, neither reflects the dynamics of most natural populations over the long term.  There are several reasons for this, as we will see below.  Nonetheless, “'''r'''” is a very useful parameter in modeling (describing & predicting) population growth as an integrator of life history traits (e.g., when & how much to reproduce) and growth potential.<br><br>


'''Logistic Growth.''' <br>
'''Linear Growth Model is another density independent model'''
Exponential growth, if unchecked, could lead to unimaginable numbers of everything from bacteria to elephants. After all, the exponential rate of population increase is proportional to the population size; the bigger the population gets, the faster it grows! Of course, most natural populations never achieve their potential for unlimited size; Darwin was keenly aware of this fact.  A third model, the '''logistic population growth model''', tends to be more realistic because it takes into account “environmental resistance” ('''K''') or carrying capacity. '''K''' is the maximum, or equilibrium, population size that can be sustained theoretically by the environment. When '''K''' is reached the population growth rate is zero due to a balance of births and deaths. '''K''' is influenced by resource availability, waste accumulation, and other density-dependent factors (see below).  
Linear models may be appropriate over short time intervals, but seldom describe long-term population growth because they fail to include an increasing number of reproductive individuals as the population grows. However, while exponential growth models are more realistic than the linear models, neither reflects the dynamics of most natural populations over the long term. There are several reasons for this, as we will see below. Nonetheless, “r” is a very useful parameter in modeling (describing & predicting) population growth as an integrator of life history traits (e.g., when & how much to reproduce) and growth potential.
 
'''Exponential growth''', if unchecked, could lead to unimaginable numbers of everything from bacteria to elephants. After all, the exponential rate of population increase is proportional to the population size; the bigger the population gets, the faster it grows! Of course, most natural populations never achieve their potential for unlimited size; Darwin was keenly aware of this fact.   
 
 
'''Density-dependent factors''' such as predators, quality of cover, parasites, diseases, and amount of food determine K, and therefore, may regulate populations by maintaining or restoring them to some equilibrium size.
 
'''Logistic Growth is a model of density dependent population growth that considers carrying capacity as a factor.'''
A third model, the logistic population growth model, tends to be more realistic because it takes into account “environmental resistance” (K) or carrying capacity. K is the maximum, or equilibrium, population size that can be sustained theoretically by the environment. When K is reached the population growth rate is zero due to a balance of births and deaths. K is influenced by resource availability, waste accumulation, and other density-dependent factors (see below).


In logistic population growth, '''''d''N/''d''t = r N<sub>t</sub> *[(K- N<sub>t</sub>)/K]'''<br>  
In logistic population growth, '''''d''N/''d''t = r N<sub>t</sub> *[(K- N<sub>t</sub>)/K]'''<br>  
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'''<center>N<sub>t</sub> = (N<sub>0</sub>K)/(N<sub>0</sub>+[K- N<sub>0</sub>]e<sup>-rt</sup>)</center>'''<br>
'''<center>N<sub>t</sub> = (N<sub>0</sub>K)/(N<sub>0</sub>+[K- N<sub>0</sub>]e<sup>-rt</sup>)</center>'''<br>


</blockquote>
'''Density-dependence''' is difficult to demonstrate in nature, in part because of frequent changes in environmental conditions. As a result, some ecologists refute the concept of “equilibrium” entirely and are currently interested in models based on chaos theory. Chaotic systems behave in unpredictable ways, even though the factors influencing them may be quite deterministic. As the number of such interacting factors increases, the ultimate “trajectory” a system takes, such as how a population grows, depends strongly on the starting conditions, and can be highly unpredictable. Chaos typifies many such “complex systems”.
 
'''Population growth in nature'''<br>
The models we have presented are more often representative of laboratory populations growing under controlled conditions, rather than the patterns seen in natural populations.  In the logistic model, as long as the population size (N) is less than the carrying capacity (K) the population will increase, and the rate of increase slows as N approaches K. However, even this model is often too simple to capture the dynamics of natural populations. If you read any of the original articles by Park about ''Tribolium'' beetles, you see that the growth curves are complex and not usually predictable. It is important to understand that K in the logistic equation is fixed, but that in reality K will continually change as environmental characteristics (e.g., availability of food & space) change. <br><br> 
 
Models of natural populations must account for the complexity of multiple interacting environmental factors.  For example, in many populations, there are distinct breeding seasons and periods of growth so it becomes important to measure the population at the same time each year to take into account when the majority of births and deaths occur.  The resources supporting populations are dynamic quantities, as are habitat characteristics, interspecific competitors, predators, and pathogens. And now, natural populations are facing the challenges of rapid local and global climate change. <br><br>


'''Population Regulation'''<br>
'''Density-dependent''' factors such as predators, quality of cover, parasites, diseases, and amount of food determine K, and therefore, may regulate populations by maintaining or restoring them to some equilibrium size.<br><br>


'''Density-independent''' factors, in particular, environmental factors such as temperature, precipitation, and disturbances (e.g., fire, floods, earthquakes, tsunamis) can also alter the rate of population growth. These factors, however, are density independent because they affect a certain proportion of the population independently of population size (and largely independent of individual fitness).<br><br>
'''Population growth in nature'''
The models presented in this lab are more often representative of laboratory populations growing under controlled conditions, rather than the patterns seen in natural populations. In the logistic model, as long as the population size (N) is less than the carrying capacity (K) the population will increase, and the rate of increase slows as N approaches K. However, even this model is often too simple to capture the dynamics of natural populations. If you read any of the original articles by Park about Tribolium beetles, you see that the growth curves are complex and not usually predictable. It is important to understand that K in the logistic equation is fixed, but that in reality K will continually change as environmental characteristics (e.g., availability of food & space) change.  


Density-dependence is difficult to demonstrate in nature, in part because of frequent changes in environmental conditions. As a result, some ecologists refute the concept of “equilibrium” entirely and are currently interested in models based on chaos theory.  Chaotic systems behave in unpredictable ways, even though the factors influencing them may be quite deterministic.  As the number of such interacting factors increases, the ultimate “trajectory” a system takes, such as how a population grows, depends strongly on the starting conditions, and can be highly unpredictable. Chaos typifies many such “complex systems”.
Models of natural populations must account for the complexity of multiple interacting environmental factors. For example, in many populations, there are distinct breeding seasons and periods of growth so it becomes important to measure the population at the same time each year to take into account when the majority of births and deaths occur. The resources supporting populations are dynamic quantities, as are habitat characteristics, interspecific competitors, predators, and pathogens. And now, natural populations are facing the challenges of rapid local and global climate change.


=='''Modeling Population Growth using Excel'''==
=='''Modeling Population Growth using Excel'''==
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