This model is a classic simulation of the production cycle in the ocean, including the effects of the thermocline in switching off advection of dissolved nutrients and detritus to the surface layer.  It illustrates a number of interesting features including the coupling of three state variables in a
This model is a classic simulation of the production cycle in the ocean, including the effects of the thermocline in switching off advection of dissolved nutrients and detritus to the surface layer.

It illustrates a number of interesting features including the coupling of three state variables in a closed cycle, the use of time to control the duration of advection, and the modulus function for cycling annual temperature data over multiple years.

The model state variables are expressed in nitrogen units (mg N m-3), and the calibration is based on:

Baliño, B.M. 1996. Eutrophication of the North Sea, 1980-1990: An evaluation of anthropogenic nutrient inputs using a 2D phytoplankton production model. Dr. scient. thesis, University of Bergen.
 
Fransz, H.G. & Verhagen, J.H.G. 1985. Modelling Research on the Production Cycle of Phytoplankton in the Southern Bight of the Northn Sea in Relation to Riverborne Nutrient Loads. Netherlands Journal of Sea Research 19 (3/4): 241-250.

This model was first implemented in PowerSim some years ago by one of my M.Sc. students, who then went on to become a Buddhist monk. Although this is a very Zen model, as far as I'm aware, the two facts are unrelated.
Model created by Scott Fortmann-Roe.  This model illustrates predator prey interactions using real-life data of wolf and moose populations on the Isle Royale.  Experiment with adjusting the initial number of moose and wolves on the island.
Model created by Scott Fortmann-Roe.  This model illustrates predator prey interactions using real-life data of wolf and moose populations on the Isle Royale.

Experiment with adjusting the initial number of moose and wolves on the island.
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]
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.


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]
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.


Simulates Ag biogeochemical cycling using data from Rauch and Pacyna 
(2009). This Insight forms part of the 
engaged lear​ning exercise for a SESYNC case study about the human relationship with silver as a natural resource 
throughout history.
Simulates Ag biogeochemical cycling using data from Rauch and Pacyna (2009). This Insight forms part of the engaged lear​ning exercise for a SESYNC case study about the human relationship with silver as a natural resource throughout history.
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]
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.


Simple model illustrating the population dynamics equation:  dn(s,t)/dt = -d[n(s,t)g(s,t)]/ds - u(s)n(s,t)  s: Weight (g) t: Time n: Number of individuals of weight s g: Scope for growth (g day-1) u: Mortality rate (day-1)
Simple model illustrating the population dynamics equation:

dn(s,t)/dt = -d[n(s,t)g(s,t)]/ds - u(s)n(s,t)

s: Weight (g)
t: Time
n: Number of individuals of weight s
g: Scope for growth (g day-1)
u: Mortality rate (day-1)
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.
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.
 Harvested fishery with endogenous investment and ship deployment policy. Ch 9 p345-360 John Morecroft (2007) Strategic Modelling and Business Dynamics. See simpler models at IM-2990 and IM-2991

Harvested fishery with endogenous investment and ship deployment policy. Ch 9 p345-360 John Morecroft (2007) Strategic Modelling and Business Dynamics. See simpler models at IM-2990 and IM-2991

Clone of:  'Sucesion Forestal' (by Denny S. Fernandez del Viso) for subtropical forest, which in turn is a modification of 'Modeling forest succession in a northeast deciduous forest' (by Owen Stuart).   Translated to English (by Lisa Belyea)
Clone of: 
'Sucesion Forestal' (by Denny S. Fernandez del Viso) for subtropical forest, which in turn is a modification of 'Modeling forest succession in a northeast deciduous forest' (by Owen Stuart).
Translated to English (by Lisa Belyea)
This model illustrates predator prey interactions using real-life data of wolf and moose populations on the Isle Royale.  We incorporate logistic growth into the moose dynamics, and we replace the death flow of the moose with a kill rate modeled from the kill rate data found on the Isle Royale websi
This model illustrates predator prey interactions using real-life data of wolf and moose populations on the Isle Royale.

We incorporate logistic growth into the moose dynamics, and we replace the death flow of the moose with a kill rate modeled from the kill rate data found on the Isle Royale website.

I start with these parameters:
Wolf Death Rate = 0.15
Wolf Birth Rate = 0.0187963
Moose Birth Rate = 0.4
Carrying Capacity = 2000
Initial Moose: 563
Initial Wolves: 20

I used RK-4 with step-size 0.1, from 1959 for 60 years.

The moose birth flow is logistic, MBR*M*(1-M/K)
Moose death flow is Kill Rate (in Moose/Year)
Wolf birth flow is WBR*Kill Rate (in Wolves/Year)
Wolf death flow is WDR*W

This model is a classic simulation of the production cycle in the ocean, including the effects of the thermocline in switching off advection of dissolved nutrients and detritus to the surface layer.  It illustrates a number of interesting features including the coupling of three state variables in a
This model is a classic simulation of the production cycle in the ocean, including the effects of the thermocline in switching off advection of dissolved nutrients and detritus to the surface layer.

It illustrates a number of interesting features including the coupling of three state variables in a closed cycle, the use of time to control the duration of advection, and the modulus function for cycling annual temperature data over multiple years.

The model state variables are expressed in nitrogen units (mg N m-3), and the calibration is based on:

Baliño, B.M. 1996. Eutrophication of the North Sea, 1980-1990: An evaluation of anthropogenic nutrient inputs using a 2D phytoplankton production model. Dr. scient. thesis, University of Bergen.
 
Fransz, H.G. & Verhagen, J.H.G. 1985. Modelling Research on the Production Cycle of Phytoplankton in the Southern Bight of the Northn Sea in Relation to Riverborne Nutrient Loads. Netherlands Journal of Sea Research 19 (3/4): 241-250.

This model was first implemented in PowerSim some years ago by one of my M.Sc. students, who then went on to become a Buddhist monk. Although this is a very Zen model, as far as I'm aware, the two facts are unrelated.
M.Sc. in Environmental Engineering SIMA 2018 New University of Lisbon, Portugal   Model to represent oyster individual growth by simulating feeding and metabolism. Model (i) partitions metabolic costs into feeding and fasting catabolism; (ii) adds allometry to clearance rate; (iii) adds temperature
M.Sc. in Environmental Engineering SIMA 2018
New University of Lisbon, Portugal

 Model to represent oyster individual growth by simulating feeding and metabolism. Model (i) partitions metabolic costs into feeding and fasting catabolism; (ii) adds allometry to clearance rate; (iii) adds temperature dependence to clearance rate; (iv) illustrates how coupled model requires a substantial volume of water (a single oyster typically clears 20-30 m3 of water in one growth cycle)
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-se
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.
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 version adds diagenesis, using an extra state variable (ph
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 version adds diagenesis, using an extra state variable (phosphorus in the sediment) and incorporates desorption processes that release phosphorus trapped in the sediment back to the water column.

The temporal dynamics of the model simulate the typical development of pollution in time.

1. Low loading, low P concentration in lake
2. High loading, increasing P concentration in lake
3. Desorption rate is low, P in sediment increases
4. Measures implemented for source control, loading reduces
5. P in lake gradually decreases, but below a certain point, desorption increases, and lake P concentration does not improve
6. Recovery only occurs when the secondary load in the sediment is strongly reduced.
This diagram provides a stylised description of important feedbacks within a shallow-lake system.     Mahinga Kai
This diagram provides a stylised description of important feedbacks within a shallow-lake system.
Mahinga Kai
Primitives for Watershed modeling project. Click Clone Insight at the top right to make a copy that you can edit.  The converter in this file contains precipitation for Tucson only. Tucson watersheds are Arroyo Chico, Canada Agua, and Lower Canada del Oro.
Primitives for Watershed modeling project. Click Clone Insight at the top right to make a copy that you can edit.

The converter in this file contains precipitation for Tucson only. Tucson watersheds are Arroyo Chico, Canada Agua, and Lower Canada del Oro.
Simulates Ag biogeochemical cycling using data from Rauch and Pacyna 
(2009). This Insight forms part of the 
engaged lear​ning exercise for a SESYNC case study about the human relationship with silver as a natural resource 
throughout history.
Simulates Ag biogeochemical cycling using data from Rauch and Pacyna (2009). This Insight forms part of the engaged lear​ning exercise for a SESYNC case study about the human relationship with silver as a natural resource throughout history.