Practice DE Modeling for Rhinoceros Population

  • Thread starter HeLiXe
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In summary: You've not explained how the growth rate is determined.2) You've not explained how the population size is determined.3) You've not explained how the equation relates to the problem.4) You've not graphed the function.5) You've not explained how your model would work in practice.6) You've not explained how the model would be affected by changing assumptions.In summary, your model does not seem to fit the given information.
  • #1
HeLiXe
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This is not a homework question or anything assigned, but I would like some practice / assistance with modeling as we have not covered that in my DE class.

Homework Statement



The rhinoceros is now extremely rare. Suppose enough game preserve land is set aside so that there is sufficient room for many more rhinoceros territories than there are rhinoceroses. Consequently there will be no danger of overcrowding. However if the population is too small, the fertile adults will have difficulty finding each other when it is time to mate. Write a differential equation that models the rhinoceros population based on these assumptions. (Note that there is more than one reasonable model that fits these assumptions.)

Homework Equations





The Attempt at a Solution


Ok so if I were to model this--I would say that the rate of change in the rhinoceros population with respect to time is proportional to the size of the population times the parameter which would be the growth coefficient...and the growth coefficient would be affected if the population is small. There are no limiting resources or predators...

Independent variable = time (t)
Dependent variable = population of rhinoceroses (P)
Parameter = (k)

I've never used LaTex before -_-
so it would be basic unlimited population growth model to start with
dP/dt = kP
but I think there would need to be another parameter (g) the smallest possible population for which the adults can still meet. So if P < g then dP/dt < 0...and I'm not sure how to express that in the model :biggrin:.
 
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  • #2
Good! You defined your variables and constants.
And you set up a proper reasoning how the population expansion would be proportional to the population size.

HeLiXe said:
dP/dt = kP
but I think there would need to be another parameter (g) the smallest possible population for which the adults can still meet. So if P < g then dP/dt < 0...and I'm not sure how to express that in the model :biggrin:.

I think you just did! :smile:

Aren't you saying something like:
[tex]\frac {dP} {dt} =
\left\{ \begin{array}{ll}
< 0, & \mbox{ if } P < g \\
k P, & \mbox{ otherwise}
\end{array} \right.[/tex]

Perhaps you might consider graphing a function that describes what you need.
What kind of graph would match the function just defined?
 
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  • #3
If rhino's being to spread apart affects your model, try relating your parameter to a density function. (rhinos/area) good luck!
 
  • #4
I like Serena said:
Good! You defined your variables and constants.
And you set up a proper reasoning how the population expansion would be proportional to the population size.
Yayyy! My programming teacher done taught me well :biggrin:


I like Serena said:
I think you just did! :smile:

Aren't you saying something like:
[tex]\frac {dP} {dt} =
\left\{ \begin{array}{ll}
< 0, & \mbox{ if } P < g \\
k P, & \mbox{ otherwise}
\end{array} \right.[/tex]

Perhaps you might consider graphing a function that describes what you need.
What kind of graph would match the function just defined?
Yes this is what I am saying. I will think about the graph and mess around in Maplesoft a bit and come back with my findings :) Thanks I Like Serena!
elegysix said:
If rhino's being to spread apart affects your model, try relating your parameter to a density function. (rhinos/area) good luck!
This is very interesting, I did not think of this at all...I will see how I can implement this. I have to go, but when I come back I will post what I've come up with. Thanks elegysix.
 
  • #5
Well, here's a link to WolframAlpha, and the corresponding picture.
Somehow, I don't think this is what you had in mind! :wink:

I have set g=2, k=1/2, and the negative part to -1.
http://www.wolframalpha.com/input/?i=Piecewise[{{-1,+P+<+2}},+(1/2)+P

attachment.php?attachmentid=37048&stc=1&d=1310242802.gif


Can you pinpoint what is wrong with this graph for being a model to your problem?
 

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  • #6
I like Serena said:
Well, here's a link to WolframAlpha, and the corresponding picture.
Somehow, I don't think this is what you had in mind! :wink:

I have set g=2, k=1/2, and the negative part to -1.
http://www.wolframalpha.com/input/?i=Piecewise[{{-1,+P+<+2}},+(1/2)+P

attachment.php?attachmentid=37048&stc=1&d=1310242802.gif


Can you pinpoint what is wrong with this graph for being a model to your problem?

Sorry I like Serena...I'm studying for a chemistry exam I have on Monday. I have a slope field that resembles what I have in mind
 

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  • #7
HeLiXe said:
Sorry I like Serena...I'm studying for a chemistry exam I have on Monday. I have a slope field that resembles what I have in mind

No hurry, finish your chemistry exam first.
I have to admit that I was wondering if you had already lost interest, but for now I'll assume you just had pressing business elsewhere. :)

Now, let's take a look at your attempt.
attachment.php?attachmentid=37057&d=1310260188.png


It seems you've tried to set up the model, calculate, and show the results all in one go.
(My graph was only of the growth rate dP/dt versus population P.)
I presume your field is population P versus time t?

Assuming it is, there are a few things wrong with it.
I'll mention one: apparently the population growth is near infinite at any given time when there is a positive population!
That can't be right.
Can you point out a few other flaws?

Basically that's what modelling is about. You try to find a simple model to fit the facts.
Work it out. See if your model fits. And if it's not complete, add something to your model.
Until you cannot solve it anymore. Then you simplify the model again... :smile:
 
  • #8
I like Serena said:
No hurry, finish your chemistry exam first.
I have to admit that I was wondering if you had already lost interest, but for now I'll assume you just had pressing business elsewhere. :)

I never lose interest in math :) And modeling is something I have not figured out so I am FAR from losing interest in it :biggrin:. I will examine these things and will get back to you after my exam. We have to turn in our homework on our exam date and my prof gives 100+ problems for every chapter and they either require a lot of steps or are so simple and repetitious that it becomes a pain doing them -_-


Yes the field was dP/dt but I have to confess I did it very quickly just to give an impression of what I was idealising and I was trying to relate it to the figures you were using lol.
I definitely do not want an infinite growth at all times, I was idealising two points of equilibrium, exponential growth above the highest point and a curve declining between the highest and lowest equilibrium points and ending at the lowest point. This leads me to believe there has to be a fraction in the model with at least one variable (numerically speaking...it could be a fraction of a parameter over a variable) in the numerator and the denominator--and I am considering that along with elegysix's hint about relating the parameter to a density function, but I have not given this the attention I want to yet.
 
  • #9
So we're agreed that we'll first try to find a function that properly describes the relation between current population P and growth rate dP/dt?
(Note that this is a function and not a vector field?)

I'll leave you to it for now, and I'll look forward to your response in which you may show some incredible insight! :wink:
(Or just show you want to learn more... whatever.)

Btw, will you let us know how your chem test went?
 
  • #10
I like Serena said:
So we're agreed that we'll first try to find a function that properly describes the relation between current population P and growth rate dP/dt?
(Note that this is a function and not a vector field?)

I'll leave you to it for now, and I'll look forward to your response in which you may show some incredible insight! :wink:
(Or just show you want to learn more... whatever.)

Btw, will you let us know how your chem test went?

omg lol yes I know this is a function we are trying to define. I really should not have responded until I have given it proper thought. And I will definitely show you that I need to learn more lol this is my second attempt at modeling ever :) Will certainly let you know about the chem exam also.

And I should note I am notorious for making the simple complicated and doing things backwards lol
 
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  • #11
I like Serena said:
So we're agreed that we'll first try to find a function that properly describes the relation between current population P and growth rate dP/dt?
(Note that this is a function and not a vector field?)

I wonder now if there is something fundamentally wrong with my reasoning. Isn't a vector field defined by a function? Like the divergence of a vector field is a function? Sometimes it is easier for me to visualise the vector field if I am not sure of the model for the function or sure how the equation would look precisely in space...the vector field helps me to visualise this. I have not learned about vector fields in calculus yet, but "slope fields" in differential equations which I understand to be the same thing.
 
  • #12
In a literal sense you are right. :)

A vector field is indeed a function. A special one, where a vector is assigned to each point in the plane.
I was talking more of a regular simple function, where a scalar value (population growth) is assigned to a scalar value (population size).

So we have a simple function f(P) that describes the population growth as a (simple) function of population.

I guess you can also visualize this as a vector field, based on population P and time t.
That is, a vector field that for each time t and population P shows what the growth rate of P versus time is.
 
  • #13
I like Serena said:
So we have a simple function f(P) that describes the population growth as a (simple) function of population.
-_- The "S" word again lol

I like Serena said:
I guess you can also visualize this as a vector field, based on population P and time t.
That is, a vector field that for each time t and population P shows what the growth rate of P versus time is.

Yes this is what I was doing. I will come back to this on Tuesday or Monday evening :) Thanks for all of your help so far I like Serena :biggrin:! And thanks for the explanation.
 
  • #14
dP/dt = kP((P/g)-1)?
Because of this "However if the population is too small, the fertile adults will have difficulty finding each other when it is time to mate"
so P/g provides a ratio of the current population to the smallest possible population for which the adults can still meet. P < g then dP/dt < 0 if kP is multiplied by (P/g)-1 because if the population is greater than the smallest possible population for which adults can still meet then P/g should be > 1; if g>P then P/g<1 and if we subtract 1 from P/g when g>p then (P/g) - 1 < 0 and dP/dt<0.

I hope this makes sense I am severely lacking sleep and I feel I may be over looking something.
 
  • #15
It seems like it could be a possible model...
 
  • #16
Looks good.
Could you make a graph?
Since I like pictures. :smile:

And can you solve the DE?
 
  • #17
I like Serena said:
Looks good.
Really? lol Yayyyyy :biggrin:
I like Serena said:
Could you make a graph?
Since I like pictures. :smile:

And can you solve the DE?

Will do as soon as I finish writing up this lab :)
 
  • #18
And? Did you finish your lab? :)

Btw, you may have found it's rather hard to solve the DE.
 
  • #19
Patience is a virtue ILS :biggrin: Actually I did not finish the lab lol the Prof extended the due date because we have 4 lab reports due at the same time, so I have been working on all of them plus an extra credit assignment :biggrin: I got my DE lab back and got 100% though :) I have not even attempted to solve this equation, but have pondered it and I cannot think of how to solve it readily. Please do not give me any hints or anything yet because I have not seriously considered solving it yet. Sorry that I am taking long to get back to you with this model, but my chemistry class is coming to an end and the prof postponed some things because of the holidays, so now she is trying to cram everything in before the class ends.
 
  • #20
Whaaaat? I think you have it backward lol.
Patience is not a virtue, impatience is!
See for instance here: http://patrickg.net/the-3-virtues-of-a-programmer/

(Weren't you interested in learning how to program too? :wink:)
 
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  • #21
:rofl:

I promise I am not being lazy this time >_>

I am trying to get everything finished by Saturday and then I will be completely devoted to DE :biggrin: Although... I have been trying to sneak some of my DE skills into my chem lab reports :tongue2:
 
  • #22
I'm just now joining in this interesting thread.
HeLiXe said:
dP/dt = kP((P/g)-1)
I was going to chime in with a somewhat lengthy explanation of a suitable equation, then realized that it was equivalent in form to this one. I'll just add that I would take g=1, the reasoning is that if there are even 2 rhinos then there is a nonzero probability that they could produce offspring together.

HeLiXe said:
I have not even attempted to solve this equation, but have pondered it and I cannot think of how to solve it readily. Please do not give me any hints or anything yet because I have not seriously considered solving it yet.
I'll just mention, be prepared that you may have to solve this numerically.

EDIT: ... or go to wolfram alpha to see the solution. (The solution surprised me, but I won't spoil it for HeLiXe.)
 
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  • #23
Hey RB, welcome to this thread! :smile:
(The more the merrier.)

Redbelly98 said:
the reasoning is that if there are even 2 rhinos then there is a nonzero probability that they could produce offspring together.

Yes, but since the chance that they would meet is supposedly low, wouldn't the expectancy for the number of rhino's in the next generation be a decreasing number?
 
  • #24
Redbelly98 said:
I'm just now joining in this interesting thread.

I was going to chime in with a somewhat lengthy explanation of a suitable equation, then realized that it was equivalent in form to this one. I'll just add that I would take g=1, the reasoning is that if there are even 2 rhinos then there is a nonzero probability that they could produce offspring together.
Yes I'll take this into consideration. All lengthy explanations are welcome :biggrin:

Redbelly98 said:
(The solution surprised me, but I won't spoil it for HeLiXe.)
Thank you Redbelly98! Please no one tell me -_- i will avoid Wolfram Alpha like the plague! Thanks for putting up with me taking long to respond :biggrin: I am going through my Chem work at a good pace and should be finished tomorrow. As soon as I am done, I will be immersed in DE until Wednesday of next week =)
 
  • #25
I like Serena said:
Hey RB, welcome to this thread! :smile:
(The more the merrier.)
Thanks!

Yes, but since the chance that they would meet is supposedly low, wouldn't the expectancy for the number of rhino's in the next generation be a decreasing number?
I had the impression that we were ignoring rhinos dying, in which case the expectancy is still a slightly larger number. If we want to include dying off in the model, I am thinking we would add a term [itex]-k_2 \ p[/itex] to the differential equation:

[tex]\frac{dp}{dt} = k_1 p (p/g - 1) -k_2 \ p[/tex]

Oh, hey, wait a minute...

[tex]\begin{equation*}
\begin{split}
& = k_1 \ p \ [p/g - (1+k_2/k_1)] \\
& = k_1 \ (1+k_2/k_1) \ p \ [\frac{p}{g (1+k_2/k_1)} - 1] \\
& = k \ p \ [\frac{p}{g'} - 1]
\end{split} \end{equation*}
[/tex]
So never mind -- we get the same equation again. Mortality can be accounted for by choosing a larger value for g.

HeLiXe said:
All lengthy explanations are welcome :biggrin:
Okay, here is what I was thinking:

1. The probability that a single rhino meets another rhino and reproduces (in some time interval) is proportional to the density of rhinos (or to the number of rhinos, if we take the land area to be a fixed parameter).

2. The rate of population growth is proportional to the number of rhinos, and to the probability that a single rhino reproduces, i.e. [itex]\frac{dp}{dt}=kp^2[/itex]

3. If we modify the probability that a single rhino reproduces to include a threshold, or include a mortality rate, we get [itex]\frac{dp}{dt}=kp(p/g - 1)[/itex] instead.
 
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  • #26
Redbelly98 said:
Thanks!I had the impression that we were ignoring rhinos dying, in which case the expectancy is still a slightly larger number. If we want to include dying off in the model, I am thinking we would add a term [itex]-k_2 \ p[/itex] to the differential equation:

[tex]\frac{dp}{dt} = k_1 p (p/g - 1) -k_2 \ p[/tex]

Oh, hey, wait a minute...

[tex]\begin{equation*}
\begin{split}
& = k_1 \ p \ [p/g - (1+k_2/k_1)] \\
& = k_1 \ (1+k_2/k_1) \ p \ [\frac{p}{g (1+k_2/k_1)} - 1] \\
& = k \ p \ [\frac{p}{g'} - 1]
\end{split} \end{equation*}
[/tex]
So never mind -- we get the same equation again. Mortality can be accounted for by choosing a larger value for g.
How did you get g' ?
Redbelly98 said:
Okay, here is what I was thinking:

1. The probability that a single rhino meets another rhino and reproduces (in some time interval) is proportional to the density of rhinos (or to the number of rhinos, if we take the land area to be a fixed parameter).

2. The rate of population growth is proportional to the number of rhinos, and to the probability that a single rhino reproduces, i.e. [itex]\frac{dp}{dt}=kp^2[/itex]

3. If we modify the probability that a single rhino reproduces to include a threshold, or include a mortality rate, we get [itex]\frac{dp}{dt}=kp(p/g - 1)[/itex] instead.

Ahh so this is what elegysix meant by the density function. Coincidentally I was looking over this last night and noticed it is an odd numbered problem and the answer given by the text is the model you described in #3. They also indicate that there are many more correct models for this scenario...maybe this one is correcter :tongue2:

Still I am having trouble with land being a fixed parameter here ... how is it indicated in the model? Or better stated how is it defined? I have never encountered the term "fixed parameter." I did some searching last night and can only find it related to algorithms in programming--if I try to translate what I read about fixed parameters in programming to this model I would think that land as a fixed parameter is indicated by the value of g in the function...(g-1).
 
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  • #27
Hi HeLiXe! :smile:

HeLiXe said:
How did you get g' ?

RB defined [itex]g' = g(1+k2/k1)[/itex].

g' is a new constant (not a derivative), which is made up of the 3 original constants (also called parameters).
HeLiXe said:
it is an odd numbered problem

What do you mean by "an odd numbered problem"?
HeLiXe said:
Still I am having trouble with land being a fixed parameter here ... how is it indicated in the model? Or better stated how is it defined? I have never encountered the term "fixed parameter." I did some searching last night and can only find it related to algorithms in programming--if I try to translate what I read about fixed parameters in programming to this model I would think that land as a fixed parameter is indicated by the value of g in the function...(g-1).

A fixed parameter for the model would be any constant related to the problem.

In this case the problem states "However if the population is too small, the fertile adults will have difficulty finding each other when it is time to mate. "

But what is "too small"?
This sentence hides a number of parameters.
One is land size, which is supposedly "large enough".

This is indeed captured in your parameter "g", but it probably is also part of your parameter "k".
Somehow g will be dependent on land size.
Because if the land size increases, logically g will increase as well.
However, there is no need (at this stage) to specify how g depends on land size.

RB is calling it a "fixed" parameter to emphasize that the parameter "land size" won't change, and that there is no need to define it as a separate parameter to the model.
 
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  • #28
HeLiXe said:
How did you get g' ?
Just combining constants from the previous equation:
[tex]g' = g(1+\frac{k_2}{k_1})[/tex]
Ahh so this is what elegysix meant by the density function. Coincidentally I was looking over this last night and noticed it is an odd numbered problem and the answer given by the text is the model you described in #3. They also indicate that there are many more correct models for this scenario...maybe this one is correcter :tongue2:

Still I am having trouble with land being a fixed parameter here ... how is it indicated in the model? Or better stated how is it defined? I have never encountered the term "fixed parameter." I did some searching last night and can only find it related to algorithms in programming--if I try to translate what I read about fixed parameters in programming to this model I would think that land as a fixed parameter is indicated by the value of g in the function...(g-1).

"Fixed parameter" is redundant, I guess, since parameters are normally held fixed anyway while the variables, uh, vary. But land area is not one of the explicit parameters in this problem -- k and g are. Somehow the area is incorporated in one or both of them.

Thinking about the "growth rate" for a single rhino (in a population of many), we might expect it depends on two things:

  1. The probability of meeting another rhino and mating successfully, which is proportional to population density p/A. (Here is where the land area explicitly comes into play.) Call this growth rate (or probability) kp/A.
  2. The probability that the rhino dies, which we can take to be constant for simplicity. Call this g.

So we get [itex]k \frac{p}{A} - g[/itex] as the growth "per rhino", per unit time. Multiply that by p, the total number of rhinos, to get the growth rate of the entire population:

[tex]\frac{dp}{dt}=p(kp/A - g)[/tex]

we can rearrange things and combine the constants, so that A gets incorporated into k, in which case it won't explicitly appear in the equation.

Also, it's instructive to have the factor in parentheses in the form [itex](p/g' - 1)[/itex]. Then we see immediately see that p=g' represents a "break even" point for the population, where births and deaths exactly balance out. Of course, g' here is the g you had written earlier, and it can depend on things like mortality rate and land area.

Hope that helps. By now in this thread we've seen several different forms for the dp/dt equation, but they're essentially the same, just with different definitions of the constants.
 
  • #29
I like Serena said:
What do you mean by "an odd numbered problem"?
It is a problem from a textbook. It's customary (in the USA, at least) for textbooks to have answers to odd-numbered problems, but not even-numbered ones, in the back of the book. Then professors have a choice of assigning problems where students either can or cannot check their answers before turning in a homework assignment.
 
  • #30
I like Serena said:
Hi HeLiXe! :smile:



RB defined [itex]g' = g(1+k2/k1)[/itex].

g' is a new constant (not a derivative), which is made up the 3 original constants (also called parameters).
Ahhhhh okay I totally missed that! I was thinking g prime as in a derivative.




I like Serena said:
What do you mean by "an odd numbered problem"?

The starting rhinoceros scenario is an exercise from my textbook and the answers to the odd numbered exercises are in the back of the book, this one has just the equation as redbelly had in #3. I thought this was an even numbered problem.


I like Serena said:
A fixed parameter for the model would be any constant related to the problem.

In this case the problem states "However if the population is too small, the fertile adults will have difficulty finding each other when it is time to mate. "

But what is "too small"?
This sentence hides a number of parameters.
One is land size, which is supposedly "large enough".

This is indeed captured in your parameter "g", but it probably is also part of your parameter "k".
Somehow g will be dependent on land size.
Because if the land size increases, logically g will increase as well.
However, there is no need (at this stage) to specify how g depends on land size.

RB is calling it a "fixed" parameter to emphasize that the parameter "land size" won't change, and that there is no need to define it as a separate parameter to the model.

OK I totally get it...I was actually thinking along these lines at first since I did not see a parameter added, but then I looked it up and started to make my own definition lol Thanks for explaining this for me!
 
  • #31
And?
Did you try to solve the DE?

As it is you have a model that satisfies the constraints of the problem, but which is hard to solve.

An alternative road is to simplify the model.
Any ideas on that?

(Btw, there's nothing wrong with doing both! :tongue:)
 
  • #32
Hi redbelly,
I was a bit impatient and asked ILS to answer me lol. I was trying to be patient, but I really wanted to know what a fixed parameter is.

Redbelly98 said:
"Fixed parameter" is redundant, I guess, since parameters are normally held fixed anyway while the variables, uh, vary.
lolololl
Redbelly98 said:
But land area is not one of the explicit parameters in this problem -- k and g are. Somehow the area is incorporated in one or both of them.

Thinking about the "growth rate" for a single rhino (in a population of many), we might expect it depends on two things:

  1. The probability of meeting another rhino and mating successfully, which is proportional to population density p/A. (Here is where the land area explicitly comes into play.) Call this growth rate (or probability) kp/A.
  2. The probability that the rhino dies, which we can take to be constant for simplicity. Call this g.

So we get [itex]k \frac{p}{A} - g[/itex] as the growth "per rhino", per unit time. Multiply that by p, the total number of rhinos, to get the growth rate of the entire population:

[tex]\frac{dp}{dt}=p(kp/A - g)[/tex]

we can rearrange things and combine the constants, so that A gets incorporated into k, in which case it won't explicitly appear in the equation.

Also, it's instructive to have the factor in parentheses in the form [itex](p/g' - 1)[/itex]. Then we see immediately see that p=g' represents a "break even" point for the population, where births and deaths exactly balance out. Of course, g' here is the g you had written earlier, and it can depend on things like mortality rate and land area.

Hope that helps. By now in this thread we've seen several different forms for the dp/dt equation, but they're essentially the same, just with different definitions of the constants.

Excellent this is a very good explanation.

When you say that we can rearrange things and combine A into k...how is this done? I am not asking for you to work it out for me, just an indication of what you mean exactly.
 
  • #33
And since I like pictures, here's a graph of our current model (k=2, g=10).
It's a graph with P on the horizontal axis, and dP/dt on the vertical axis.
I like to think of dP/dt as the change in population in one generation.

http://www.wolframalpha.com/input/?i=Plot[2+p+(p+/+10+-+1),+{p,+-10,+30}]
attachment.php?attachmentid=37240&stc=1&d=1310869948.gif


I'll just point out a few things to note.

1. At P=0, the population remains constant at zero, which is good.

2. At P=10, the population remains constant as well, which is our break even point (g).

3. At P=5, the population halves in the next generation, which sounds about right.

4. At P=20, the population triples in one generation, I think I overdid the parameter k.

5. At P=30, the population is quintupled in one generation, which is too much I think.
And at higher population sizes, this "problem" becomes unrealistically worse.

6. For negative P, the population increases, which is not right.
So we should set the model for instance to zero for negative P.
 

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  • #34
I like Serena said:
And?
Did you try to solve the DE?
Well ...you may be partially pleased to know that I have finally started working on it lol

I like Serena said:
As it is you have a model that satisfies the constraints of the problem, but which is hard to solve.

An alternative road is to simplify the model.
Any ideas on that?

(Btw, there's nothing wrong with doing both! :tongue:)

I will give it some thought and continue with trying to work this one out since I just started with it.
 
  • #35
Should not this be a two variable problem? If I remember well, there has to be a male and a female to produce a baby, but only females can give birth. So the growth rates of both male and female rhinos are proportional to the probability that a female rhino meets a male during the mating period, and the number of female rhinos.
The baby can be a male or female, say, with equal probability and you have to subtract the dying rate. But it can be even more complicated than that. :wink:

ehild
 

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