In Chile, 60% of its population are exposed to levels of Particulate Matter (PM) above international standards. Air Pollution is causing 4,000 premature deaths per year, including health costs over US$8 billion.

Overview: 

This model implements the one-dimensional version of the advection-dispersion equation for an estuary. The equation is:

dS/dt = (1/A)d(QS)/dx - (1/A)d(EA)/dx(dS/dx) (Eq. 1)

Where S: salinity (or any other constituent such as chlorophyll or dissolved oxygen), (e.g. kg m-3); t: time (s); A: cross-sectional area (m2); Q: river flow (m3 s-1); x: length of box (m); E: dispersion coefficient (m2 s-1).

For a given length delta x, Adx = V, the box volume. For a set value of Q, the equation becomes:

VdS/dt = QdS - (d(EA)/dx) dS (Eq. 2)

EA/x, i.e. (m2 X m2) / (m s) = E(b), the bulk dispersion coefficient, units in m3 s-1, i.e. a flow, equivalent to Q

At steady state, dS/dt = 0, therefore we can rewrite Eq. 2 for one estuarine box as:

Q(Sr-Se)=E(b)r,e(Sr-Se)-E(b)e,s(Se-Ss) (Eq. 3)

Where Sr: river salinity (=0), Se: mean estuary salinity; Ss: mean ocean salinity

E(b)r,e: dispersion coefficient between river and estuary, and E(b)e,s: dispersion coefficient between the estuary and ocean.

By definition the value of E(b)r,e is zero, otherwise we are not at the head (upstream limit of salt intrusion) of the estuary. Likewise Sr is zero, otherwise we're not in the river. Therefore:

QSe=E(b)e,s(Se-Ss) (Eq. 4)

At steady state

E(b)e,s = QSe/(Se-Ss) (Eq 5)

The longitudinal dispersion simulates the turbulent mixiing of water in the estuary during flood and ebb, which supplies salt water to the estuary on the flood tide, and make the sea a little more brackish on the ebb.

You can use the slider to turn off dispersion (set to zero), and see that if the tidal wave did not mix with the estuary water due to turbulence, the estuary would quickly become a freshwater system.

This diagram provides an accessible description of the key processes that influence the water quality within a lake.

Life and Death

Simple mass balance model for lakes, based on the Vollenweider equation:

dMw/dt = Min - sMw - Mout

The model was first used in the 1960s to determine the phosphorus concentration in lakes and reservoirs, for eutrophication assessment.

This model describes the flow of energy from generation to consumption for neighborhoods in the metro Atlanta area. It also calculates the cost of energy production and the number of years it will take to recover that cost.

In Chile, 60% of its population are exposed to levels of Particulate Matter (PM) above international standards. Air Pollution is causing 4,000 premature deaths per year, including health costs over US$8 billion.

HANDY Model of Societal Collapse from Ecological Economics Paper 

 The effect of phosphorus on an ecosystem

March 12, 2019

This model uses simple functions (converters, cosine) to simulate the water balance inside a reservoir.

A system dynamics model of a predator-prey lifecycle relationship

This model uses simple functions (converters, cosine) to simulate the water balance inside a reservoir.

This diagram provides a stylised description of important feedbacks within a shallow-lake system.

Simple model to illustrate oyster growth based on primary production of Phytoplankton as a state variable, forced by light and nutrients, running for a yearly period.

Phytoplankton growth based on on Steele's and Michaelis-Menten equations), where: 

Primary Production=(([Pmax]*[I]/[Iopt]*exp(1-[I]/[Iopt])*[S])/([Ks]+[S]))

Pmax: Maximum production (d-1)
I: Light energy at depth of interest (uE m-2 s-1)
Iopt: Light energy at which Pmax occurs (uE m-2 s-1)
S: Nutrient concentration (umol N L-1)
Ks: Half saturation constant for nutrient (umol N L-1).

Further developments:
- Nutrients as state variable in cycle with detritus from phytoplankton and oyster biomass.
- Light limited by the concentration of phytoplankton.
- Temperature effect on phytoplankton and Oyster growth.

General global ocean box model, including isotopes.

Very simple model demonstrating growth of phytoplankton using Steele's equation for potential production and Michaelis-Menten equation for nutrient limitation.

Both light and nutrients (e.g. nitrogen) are modelled as forcing functions, and the model is "over-calibrated" for stability.

The phytoplankton model approximately reproduces the spring-summer diatom bloom and the (smaller) late summer dinoflagellate bloom.
 
Oyster growth is modelled only as a throughput from algae. Further developments would include filtration as a function of oyster biomass, oyster mortality, and other adjustments.

European Masters in System Dynamics 2016
New University of Lisbon, Portugal

Simple model to represent oyster individual growth by simulating feeding and metabolism.

Simple (Kind of) food web of the Cane Toad Species. Includes different levels of consumers including predators.

Very simple model demonstrating growth of phytoplankton using Steele's equation for potential production and Michaelis-Menten equation for nutrient limitation.

Both light and nutrients (e.g. nitrogen) are modelled as forcing functions, and the model is "over-calibrated" for stability.

The phytoplankton model approximately reproduces the spring-summer diatom bloom and the (smaller) late summer dinoflagellate bloom.
 
Oyster growth is modelled only as a throughput from algae. Further developments would include filtration as a function of oyster biomass, oyster mortality, and other adjustments.

This is an edited copy of the original simple building heat flow. I addressed the insulation aspect of this problem by reducing the conductivity values of both the walls and windows. To address a chiller system, I integrated mechanical cooling into the process. To address solar panels, I calculated the effect they may have on electricity prices by adding Solar Panel variables to the equation.

This non-dimensionalized, sleekest most neatest model illustrates predator prey interactions using logistic growth for the moose population, for the wolf and moose populations on Isle Royale.

Thanks Scott Fortmann-Roe for the original model.

I've added in an adjustment to handle population sizes, by dividing by moose carrying capacity.

Time is scaled by the moose birth parameter:
tau=bm*t

There are therefore only three parameters left to account for any dynamics:

beta = bw/bm (relative wolf to moose births)
delta = dm/bm (relative death to birth ratio for moose)
gamma = dw/bm (wolf deaths to moose births)

The equations are thus

dM/dtau = M [ (1-M) - delta W ]
dW/dtau = W [beta M - gamma ]

There is a stable equilibrium pair of population values, relative to the carrying capacity:

M^* = gamma / beta
W^* = (1-gamma / beta) / delta

I have a sleek version with a logistical growth term for the moose, at

http://www.nku.edu/~longa/classes/2018spring/mat375/mathematica/Moose-n-Wolf-InsightMaker-sleek.nb