This is a first example of a simple SIR (Susceptible, Infected, Recovered) model. There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again
Mat375 Math Modeling SIR
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model.

There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again.

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel.nb

Clone of A Simple SIR (Susceptible, Infected, Recovered) Example
Jon Ford
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ Next up: and SIR, and his interesting model of female birth weights.
Markov Chain Mat375 Olinick
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

Next up: and SIR, and his interesting model of female birth weights.
Clone of Flakes no more!
Sally Dufek
This simple model demonstrates logistic growth.The differential equation looks like y'(t)=by(t)(1-y(t)/K) where K is the carrying capacity of the quantity y. Alternatively, y'(t)=by(t) - b/K*y(t)^2 so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t
Math Modeling Mat375
This simple model demonstrates logistic growth.The differential equation looks like

y'(t)=by(t)(1-y(t)/K)

where K is the carrying capacity of the quantity y. Alternatively,

y'(t)=by(t) - b/K*y(t)^2

so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t) -- loss is proportional to population (crowding).

A comparable Mathematica file is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/LogisticGrowth-and-DecayModel.nb
Clone of Logistic Growth
luke vanlaningham
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ Next up: and SIR, and his interesting model of female birth weights.
Olinick Mat375 Markov Chain
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

Next up: and SIR, and his interesting model of female birth weights.
Clone of Flakes no more!
Maria E Ruwe
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al . in A Course in Mathematical Biology. They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that different
Math Modeling Mat375 SIR
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al. in A Course in Mathematical Biology.

They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that differential equations are generally solved numerically by discretizing them, so that the comparison is a little bit rigged....

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel-w-discrete-version.nb

Clone of A Simple Infection-only SIR (Susceptible, Infected, Recovered) Example
Lizzy Compton
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al . in A Course in Mathematical Biology. They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that different
Math Modeling Mat375 SIR
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al. in A Course in Mathematical Biology.

They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that differential equations are generally solved numerically by discretizing them, so that the comparison is a little bit rigged....

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel-w-discrete-version.nb

Clone of Clone of A Simple Infection-only SIR (Susceptible, Infected, Recovered) Example
Jiangkun Wang
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model. There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again
Math Modeling Mat375 SIR
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model.

There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again.

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel.nb

Clone of A Simple SIR (Susceptible, Infected, Recovered) Example
Kate Quinn
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al . in A Course in Mathematical Biology. They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that different
SIR Mat375 Math Modeling
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al. in A Course in Mathematical Biology.

They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that differential equations are generally solved numerically by discretizing them, so that the comparison is a little bit rigged....

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel-w-discrete-version.nb

Clone of A Simple Infection-only SIR (Susceptible, Infected, Recovered) Example
Matthew Gall
This simple model demonstrates logistic growth.The differential equation looks like y'(t)=by(t)(1-y(t)/K) where K is the carrying capacity of the quantity y. Alternatively, y'(t)=by(t) - b/K*y(t)^2 so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t
Mat375 Math Modeling
This simple model demonstrates logistic growth.The differential equation looks like

y'(t)=by(t)(1-y(t)/K)

where K is the carrying capacity of the quantity y. Alternatively,

y'(t)=by(t) - b/K*y(t)^2

so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t) -- loss is proportional to population (crowding).

A comparable Mathematica file is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/LogisticGrowth-and-DecayModel.nb
Clone of Logistic Growth
Thomas Browe
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ Next up: and SIR, and his interesting model of female birth weights.
Mat375 Olinick Markov Chain
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

Next up: and SIR, and his interesting model of female birth weights.
Clone of Flakes no more!
Maria E Ruwe
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators ( Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the
Math Modeling Mat375
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators (Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the cycling of the populations in nature.

The differential equations for the population of hare (x) is

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha y x/(x+mu)

where K is the logistic carrying capacity of the prey (hare), in the absence of predation; the second term is a "generalist predation" term;  and the third term is the "specialist predation" (in the limit as the prey gets big, this becomes simply proportional to y (the lynx population)).

The differential equations for the population of lynx (y) is

y'(t) = sy(1- qy/x) = sy - sqy^2/x

for the predator (lynx), which is essentially logistic growth. Its growth term suggests exponential growth, but there is a loss term of the form sqy^2/x -- loss is proportional to population (crowding), and inversely proportional to prey density. As the hare population goes to zero, so shall the lynx....

As one can see, the prey density won't change if y=x/q. If the prey density were not changing at the same time, the system would be at equilibrium.

In this InsightMaker model, I scaled the second equation by multiplying by q, then replace y by w=qy throughout both equations. This requires a slight change in the prey equation -- alpha replaced by the ratio of alpha/q.  (I used my favorite mathematical trick, of multiplying by the appropriate form of 1!)

So what we're really looking at here is the system

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha/q w x/(x+mu)
w'(t) = sw(1- w/x)

where w(t)=qy(t).

Tyson, et al. took q to be about 212 for hare and lynx -- so that it requires about 212 hare to allow for one lynx to survive at "equilibrium".

However, when alpha -- the hares/lynx/year -- gets sufficiently large (e.g. 1867 -- and that does seem like a lot of hares per lynx per year...:), limit cycles develop (rather than a stable equilibrium). This means that the populations oscillate about the equilibrium values, rather than stabilize at those values.

Author: Andy Long, Northern Kentucky University (2020)

Reference: Tyson, Rebecca, Sheena Haines,  Karen Hodges. Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators. Theoretical Ecology. 3, 97–111 (2010). https://doi.org/10.1007/s12080-009-0057-1

Resource: A comparable Mathematica model can be found at  http://ceadserv1.nku.edu/longa//classes/mat375/days/Mathematica/BasicModel.nb,
which allows one to experiment a little more easily than one can with this InsightMaker model.
Clone of Basic Model, Tyson Lynx and Hare
Cameron Demler
This simple model demonstrates logistic growth.The differential equation looks like y'(t)=by(t)(1-y(t)/K) where K is the carrying capacity of the quantity y. Alternatively, y'(t)=by(t) - b/K*y(t)^2 so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t
Math Modeling Mat375
This simple model demonstrates logistic growth.The differential equation looks like

y'(t)=by(t)(1-y(t)/K)

where K is the carrying capacity of the quantity y. Alternatively,

y'(t)=by(t) - b/K*y(t)^2

so the growth term suggests exponential growth, but there is a loss term is of the form b/K y(t) -- loss is proportional to population (crowding).

A comparable Mathematica file is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/LogisticGrowth-and-DecayModel.nb
Clone of Logistic Growth
Thomas Browe
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators ( Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the
Mat375 Math Modeling
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators (Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the cycling of the populations in nature.

The differential equations for the population of hare (x) is

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha y x/(x+mu)

where K is the logistic carrying capacity of the prey (hare), in the absence of predation; the second term is a "generalist predation" term;  and the third term is the "specialist predation" (in the limit as the prey gets big, this becomes simply proportional to y (the lynx population)).

The differential equations for the population of lynx (y) is

y'(t) = sy(1- qy/x) = sy - sqy^2/x

for the predator (lynx), which is essentially logistic growth. Its growth term suggests exponential growth, but there is a loss term of the form sqy^2/x -- loss is proportional to population (crowding), and inversely proportional to prey density. As the hare population goes to zero, so shall the lynx....

As one can see, the prey density won't change if y=x/q. If the prey density were not changing at the same time, the system would be at equilibrium.

In this InsightMaker model, I scaled the second equation by multiplying by q, then replace y by w=qy throughout both equations. This requires a slight change in the prey equation -- alpha replaced by the ratio of alpha/q.  (I used my favorite mathematical trick, of multiplying by the appropriate form of 1!)

So what we're really looking at here is the system

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha/q w x/(x+mu)
w'(t) = sw(1- w/x)

where w(t)=qy(t).

Tyson, et al. took q to be about 212 for hare and lynx -- so that it requires about 212 hare to allow for one lynx to survive at "equilibrium".

However, when alpha -- the hares/lynx/year -- gets sufficiently large (e.g. 1867 -- and that does seem like a lot of hares per lynx per year...:), limit cycles develop (rather than a stable equilibrium). This means that the populations oscillate about the equilibrium values, rather than stabilize at those values.

Author: Andy Long, Northern Kentucky University (2020)

Reference: Tyson, Rebecca, Sheena Haines,  Karen Hodges. Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators. Theoretical Ecology. 3, 97–111 (2010). https://doi.org/10.1007/s12080-009-0057-1

Resource: A comparable Mathematica model can be found at  http://ceadserv1.nku.edu/longa//classes/mat375/days/Mathematica/BasicModel.nb,
which allows one to experiment a little more easily than one can with this InsightMaker model.
Clone of Basic Model, Tyson Lynx and Hare
Jacob Adkins
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ Next up: and SIR, and his interesting model of female birth weights.
Markov Chain Olinick Mat375
This is an introductory example from Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

Next up: and SIR, and his interesting model of female birth weights.
Clone of Flakes no more!
Christopher Milesky
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change. Actually it might be be
Mat375 Markov Chain
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change.

Actually it might be better to think of this as a poisoning model: the rate of infection is constant, and independent of the existence of an infected population. That's more like disease due to an environmental effect (e.g. lead-poisoning from smelters, or mercury poisoning from the burning of coal). So infected would mean "effected", and "recovered" might be "treated" -- and ultimately released, to be exposed again.

This shows that the equilibrium does not determine the transition probabilities: two different transition matrices can have the same ultimate equilibrium.

There is a constraint on the infection rate that I haven't figured out how to build in:

InfectionRate < Min[1,wi/ws, wr/ws]

I can allow InfectionRate to vary up to 1 if I take
ws < wi
and
ws < wr
However if you violate that, you'll get interesting solutions with negative values of populations. The dynamics are pretty interesting in that case, however! If you want to see them, you'll have to remove the constraints that I put on the parameters in the Recover and LossOfImmunity parameters.

Thanks Mike! Interesting examples, as always....
Andy Long

Driehaus SIR (poisoning would be better) Markov Model
Rachel Driehaus
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators ( Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the
Mat375 Math Modeling
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators (Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the cycling of the populations in nature.

The differential equations for the population of hare (x) is

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha y x/(x+mu)

where K is the logistic carrying capacity of the prey (hare), in the absence of predation; the second term is a "generalist predation" term;  and the third term is the "specialist predation" (in the limit as the prey gets big, this becomes simply proportional to y (the lynx population)).

The differential equations for the population of lynx (y) is

y'(t) = sy(1- qy/x) = sy - sqy^2/x

for the predator (lynx), which is essentially logistic growth. Its growth term suggests exponential growth, but there is a loss term of the form sqy^2/x -- loss is proportional to population (crowding), and inversely proportional to prey density. As the hare population goes to zero, so shall the lynx....

As one can see, the prey density won't change if y=x/q. If the prey density were not changing at the same time, the system would be at equilibrium.

In this InsightMaker model, I scaled the second equation by multiplying by q, then replace y by w=qy throughout both equations. This requires a slight change in the prey equation -- alpha replaced by the ratio of alpha/q.  (I used my favorite mathematical trick, of multiplying by the appropriate form of 1!)

So what we're really looking at here is the system

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha/q w x/(x+mu)
w'(t) = sw(1- w/x)

where w(t)=qy(t).

Tyson, et al. took q to be about 212 for hare and lynx -- so that it requires about 212 hare to allow for one lynx to survive at "equilibrium".

However, when alpha -- the hares/lynx/year -- gets sufficiently large (e.g. 1867 -- and that does seem like a lot of hares per lynx per year...:), limit cycles develop (rather than a stable equilibrium). This means that the populations oscillate about the equilibrium values, rather than stabilize at those values.

Author: Andy Long, Northern Kentucky University (2020)

Reference: Tyson, Rebecca, Sheena Haines,  Karen Hodges. Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators. Theoretical Ecology. 3, 97–111 (2010). https://doi.org/10.1007/s12080-009-0057-1

Resource: A comparable Mathematica model can be found at  http://ceadserv1.nku.edu/longa//classes/mat375/days/Mathematica/BasicModel.nb,
which allows one to experiment a little more easily than one can with this InsightMaker model.
Clone of Basic Model, Tyson Lynx and Hare
Cameron Demler
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change. Actually it might be be
Mat375 Markov Chain
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change.

Actually it might be better to think of this as a poisoning model: the rate of infection is constant, and independent of the existence of an infected population. That's more like disease due to an environmental effect (e.g. lead-poisoning from smelters, or mercury poisoning from the burning of coal). So infected would mean "effected", and "recovered" might be "treated" -- and ultimately released, to be exposed again.

This shows that the equilibrium does not determine the transition probabilities: two different transition matrices can have the same ultimate equilibrium.

There is a constraint on the infection rate that I haven't figured out how to build in:

InfectionRate < Min[1,wi/ws, wr/ws]

I can allow InfectionRate to vary up to 1 if I take
ws < wi
and
ws < wr
However if you violate that, you'll get interesting solutions with negative values of populations. The dynamics are pretty interesting in that case, however! If you want to see them, you'll have to remove the constraints that I put on the parameters in the Recover and LossOfImmunity parameters.

Thanks Mike! Interesting examples, as always....
Andy Long

Clone of SIR (poisoning would be better) Markov Model
Alyssa Farmer
Spring, 2020: in the midst of on-line courses, due to the pandemic of Covid-19. With the onset of the Covid-19 coronavirus crisis, we focus on SIRD models, which might realistically model the course of the disease. We start with an SIR model, such as that featured in the MAA model featured
Mat375 SIR Math Modeling COVID-19 Coronavirus SIRD
Spring, 2020: in the midst of on-line courses, due to the pandemic of Covid-19.

With the onset of the Covid-19 coronavirus crisis, we focus on SIRD models, which might realistically model the course of the disease.

We start with an SIR model, such as that featured in the MAA model featured in

Without mortality, with time measured in days, with infection rate 1/2, recovery rate 1/3, and initial infectious population I_0=1.27x10-4, we reproduce their figure

With a death rate of .005 (one two-hundredth of the infected per day), an infectivity rate of 0.5, and a recovery rate of .145 or so (takes about a week to recover), we get some pretty significant losses -- about 3.2% of the total population.

Resources:
Clone of Coronavirus: A Simple SIR (Susceptible, Infected, Recovered) with death
Eve Gross-Sable
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model. There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again
Mat375 SIR Math Modeling
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model.

There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again.

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel.nb

Clone of A Simple SIR (Susceptible, Infected, Recovered) Example
Samuel Kaelin
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators ( Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the
Mat375 Math Modeling
The basic model of Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators (Tyson, et al.) demonstrates logistic growth in prey, and in predator (with prey dependence for carrying capacity). But interestingly, one possibility is limit cycles, which mimic the cycling of the populations in nature.

The differential equations for the population of hare (x) is

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha y x/(x+mu)

where K is the logistic carrying capacity of the prey (hare), in the absence of predation; the second term is a "generalist predation" term;  and the third term is the "specialist predation" (in the limit as the prey gets big, this becomes simply proportional to y (the lynx population)).

The differential equations for the population of lynx (y) is

y'(t) = sy(1- qy/x) = sy - sqy^2/x

for the predator (lynx), which is essentially logistic growth. Its growth term suggests exponential growth, but there is a loss term of the form sqy^2/x -- loss is proportional to population (crowding), and inversely proportional to prey density. As the hare population goes to zero, so shall the lynx....

As one can see, the prey density won't change if y=x/q. If the prey density were not changing at the same time, the system would be at equilibrium.

In this InsightMaker model, I scaled the second equation by multiplying by q, then replace y by w=qy throughout both equations. This requires a slight change in the prey equation -- alpha replaced by the ratio of alpha/q.  (I used my favorite mathematical trick, of multiplying by the appropriate form of 1!)

So what we're really looking at here is the system

x'(t) = rx(1-x/K)
            - gamma x^2/(x^2+eta^2)
            - alpha/q w x/(x+mu)
w'(t) = sw(1- w/x)

where w(t)=qy(t).

Tyson, et al. took q to be about 212 for hare and lynx -- so that it requires about 212 hare to allow for one lynx to survive at "equilibrium".

However, when alpha -- the hares/lynx/year -- gets sufficiently large (e.g. 1867 -- and that does seem like a lot of hares per lynx per year...:), limit cycles develop (rather than a stable equilibrium). This means that the populations oscillate about the equilibrium values, rather than stabilize at those values.

Author: Andy Long, Northern Kentucky University (2020)

Reference: Tyson, Rebecca, Sheena Haines,  Karen Hodges. Modelling the Canada lynx and snowshoe hare population cycle: The role of specialist predators. Theoretical Ecology. 3, 97–111 (2010). https://doi.org/10.1007/s12080-009-0057-1

Resource: A comparable Mathematica model can be found at  http://ceadserv1.nku.edu/longa//classes/mat375/days/Mathematica/BasicModel.nb,
which allows one to experiment a little more easily than one can with this InsightMaker model.
Clone of Basic Model, Tyson Lynx and Hare
Thomas Browe
Spring, 2020: in the midst of on-line courses, due to the pandemic of Covid-19. With the onset of the Covid-19 coronavirus crisis, we focus on SIRD models, which might realistically model the course of the disease. We start with an SIR model, such as that featured in the MAA model featured
SIR SIRD Math Modeling COVID-19 Mat375 Coronavirus
Spring, 2020: in the midst of on-line courses, due to the pandemic of Covid-19.

With the onset of the Covid-19 coronavirus crisis, we focus on SIRD models, which might realistically model the course of the disease.

We start with an SIR model, such as that featured in the MAA model featured in

Without mortality, with time measured in days, with infection rate 1/2, recovery rate 1/3, and initial infectious population I_0=1.27x10-4, we reproduce their figure

With a death rate of .005 (one two-hundredth of the infected per day), an infectivity rate of 0.5, and a recovery rate of .145 or so (takes about a week to recover), we get some pretty significant losses -- about 3.2% of the total population.

Resources:
Clone of Coronavirus: A Simple SIR (Susceptible, Infected, Recovered) with death
Jacob Adkins
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model. There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again
SIR Mat375 Math Modeling
This is a first example of a simple SIR (Susceptible, Infected, Recovered) model.

There are three pools of individuals: those who are infected (without them, no disease!), the pool of those who are at risk (susceptible), and the recovered -- who may lose their immunity and become susceptible again.

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel.nb

Clone of A Simple SIR (Susceptible, Infected, Recovered) Example
Cameron Demler
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al . in A Course in Mathematical Biology. They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that different
SIR Mat375 Math Modeling
This is a simple example of (part of a) simple SIR (Susceptible, Infected, Recovered) model, suggested by De Vries, et al. in A Course in Mathematical Biology.

They wanted to illustrate the comparative behavior of differential equations and discrete difference equations. We know that differential equations are generally solved numerically by discretizing them, so that the comparison is a little bit rigged....

A comparable model in Mathematica is available at
http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/SIRModel-w-discrete-version.nb

Clone of A Simple Infection-only SIR (Susceptible, Infected, Recovered) Example
Jacob Englert
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences . ​ It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change. Actually it might be be
Mat375 Markov Chain
This is an example I thought of after reading Olinick's book An Introduction to Mathematical Models in the Social and Life Sciences. ​

It's an SIR-type model, but one where the equilibrium (ws,wi,wr) is always the same, even as the weights in the transition matrix change.

Actually it might be better to think of this as a poisoning model: the rate of infection is constant, and independent of the existence of an infected population. That's more like disease due to an environmental effect (e.g. lead-poisoning from smelters, or mercury poisoning from the burning of coal). So infected would mean "effected", and "recovered" might be "treated" -- and ultimately released, to be exposed again.

This shows that the equilibrium does not determine the transition probabilities: two different transition matrices can have the same ultimate equilibrium.

There is a constraint on the infection rate that I haven't figured out how to build in:

InfectionRate < Min[1,wi/ws, wr/ws]

I can allow InfectionRate to vary up to 1 if I take
ws < wi
and
ws < wr
However if you violate that, you'll get interesting solutions with negative values of populations. The dynamics are pretty interesting in that case, however! If you want to see them, you'll have to remove the constraints that I put on the parameters in the Recover and LossOfImmunity parameters.

Thanks Mike! Interesting examples, as always....
Andy Long

Clone of SIR (poisoning would be better) Markov Model
Christopher Milesky