This is a convenient wrapper function calling each of the following functions
See the Details section below for a discussion of how to use this function.
setParams(params, interaction = NULL, ...)
Optional interaction matrix of the species (predator species x prey species). Entries should be numbers between 0 and 1. By default all entries are 1. See "Setting interactions" section below.
Arguments passed on to setPredKernel
, setSearchVolume
, setMaxIntakeRate
, setMetabolicRate
, setExtMort
, setReproduction
, setFishing
, setResource
pred_kernel
Optional. An array (species x predator size x prey size) that holds the predation coefficient of each predator at size on each prey size. If not supplied, a default is set as described in section "Setting predation kernel".
search_vol
Optional. An array (species x size) holding the search volume for each species at size. If not supplied, a default is set as described in the section "Setting search volume".
intake_max
Optional. An array (species x size) holding the maximum intake rate for each species at size. If not supplied, a default is set as described in the section "Setting maximum intake rate".
metab
Optional. An array (species x size) holding the metabolic rate for each species at size. If not supplied, a default is set as described in the section "Setting metabolic rate".
p
The allometric metabolic exponent. This is only used if metab
is not given explicitly and if the exponent is not specified in a p
column in the species_params
.
ext_mort
Optional. An array (species x size) holding the external mortality rate.
z0pre
If z0
, the mortality from other sources, is not a column
in the species data frame, it is calculated as z0pre * w_inf ^ z0exp.
Default value is 0.6.
z0exp
If z0
, the mortality from other sources, is not a column
in the species data frame, it is calculated as z0pre * w_inf ^ z0exp
.
Default value is n-1
.
z0
Use
ext_mort
instead. Not to
be confused with the species_parameter z0
.
maturity
Optional. An array (species x size) that holds the proportion of individuals of each species at size that are mature. If not supplied, a default is set as described in the section "Setting reproduction".
repro_prop
Optional. An array (species x size) that holds the proportion of consumed energy that a mature individual allocates to reproduction for each species at size. If not supplied, a default is set as described in the section "Setting reproduction".
RDD
The name of the function calculating the density-dependent
reproduction rate from the density-independent rate. Defaults to
"BevertonHoltRDD()
".
selectivity
Optional. An array (gear x species x size) that holds the selectivity of each gear for species and size, \(S_{g,i,w}\).
catchability
Optional. An array (gear x species) that holds the catchability of each species by each gear, \(Q_{g,i}\).
initial_effort
Optional. A number or a named numeric vector specifying the fishing effort. If a number, the same effort is used for all gears. If a vector, must be named by gear.
resource_rate
Optional. Vector of resource intrinsic birth rates
resource_capacity
Optional. Vector of resource intrinsic carrying capacity
r_pp
Coefficient of the intrinsic resource birth rate
n
Allometric growth exponent for resource
kappa
Coefficient of the intrinsic resource carrying capacity
lambda
Scaling exponent of the intrinsic resource carrying capacity
w_pp_cutoff
The upper cut off size of the resource spectrum. The carrying capacity will be set to 0 above this size. Default is 10 g.
resource_dynamics
Optional. Name of the function that determines the
resource dynamics by calculating the resource spectrum at the next time
step from the current state. You only need to specify this if you do not
want to use the default resource_semichemostat()
.
Mizer uses grams to measure weight, centimetres to measure lengths, and years to measure time.
Mizer is agnostic about whether abundances are given as
numbers per area,
numbers per volume or
total numbers for the entire study area.
You should make the choice most convenient for your application and then stick with it. If you make choice 1 or 2 you will also have to choose a unit for area or volume. Your choice will then determine the units for some of the parameters. This will be mentioned when the parameters are discussed in the sections below.
Your choice will also affect the units of the quantities you may want to
calculate with the model. For example, the yield will be in grams/year/m^2 in
case 1 if you choose m^2 as your measure of area, in grams/year/m^3 in case 2
if you choose m^3 as your unit of volume, or simply grams/year in case 3. The
same comment applies for other measures, like total biomass, which will be
grams/area in case 1, grams/volume in case 2 or simply grams in case 3. When
mizer puts units on axes in plots, it will choose the units appropriate for
case 3. So for example in plotBiomass()
it gives the unit as grams.
You can convert between these choices. For example, if you use case 1, you
need to multiply with the area of the ecosystem to get the total quantity.
If you work with case 2, you need to multiply by both area and the thickness
of the productive layer. In that respect, case 2 is a bit cumbersome. The
function scaleModel()
is useful to change the units you are using.
Kernel dependent on predator to prey size ratio
If the pred_kernel
argument is not supplied, then this function sets a
predation kernel that depends only on the ratio of predator mass to prey
mass, not on the two masses independently. The shape of that kernel is then
determined by the pred_kernel_type
column in species_params.
The default for pred_kernel_type
is "lognormal". This will call the function
lognormal_pred_kernel()
to calculate the predation kernel.
An alternative pred_kernel type is "box", implemented by the function
box_pred_kernel()
, and "power_law", implemented by the function
power_law_pred_kernel()
. These functions require certain species
parameters in the species_params data frame. For the lognormal kernel these
are beta
and sigma
, for the box kernel they are ppmr_min
and ppmr_max
. They are explained in the help pages for the kernel
functions. Except for beta
and sigma
, no defaults are set for
these parameters. If they are missing from the species_params data frame then
mizer will issue an error message.
You can use any other string for pred_kernel_type
. If for example you
choose "my" then you need to define a function my_pred_kernel
that you can
model on the existing functions like lognormal_pred_kernel()
.
When using a kernel that depends on the predator/prey size ratio only, mizer
does not need to store the entire three dimensional array in the MizerParams
object. Such an array can be very big when there is a large number of size
bins. Instead, mizer only needs to store two two-dimensional arrays that hold
Fourier transforms of the feeding kernel function that allow the encounter
rate and the predation rate to be calculated very efficiently. However, if
you need the full three-dimensional array you can calculate it with the
getPredKernel()
function.
Kernel dependent on both predator and prey size
If you want to work with a feeding kernel that depends on predator mass and prey mass independently, you can specify the full feeding kernel as a three-dimensional array (predator species x predator size x prey size).
You should use this option only if a kernel dependent only on the predator/prey mass ratio is not appropriate. Using a kernel dependent on predator/prey mass ratio only allows mizer to use fast Fourier transform methods to significantly reduce the running time of simulations.
The order of the predator species in pred_kernel
should be the same
as the order in the species params dataframe in the params
object. If you
supply a named array then the function will check the order and warn if it is
different.
The search volume \(\gamma_i(w)\) of an individual of species \(i\)
and weight \(w\) multiplies the predation kernel when
calculating the encounter rate in getEncounter()
and the
predation rate in getPredRate()
.
The name "search volume" is a bit misleading, because \(\gamma_i(w)\) does not have units of volume. It is simply a parameter that determines the rate of predation. Its units depend on your choice, see section "Units in mizer". If you have chosen to work with total abundances, then it is a rate with units 1/year. If you have chosen to work with abundances per m^2 then it has units of m^2/year. If you have chosen to work with abundances per m^3 then it has units of m^3/year.
If the search_vol
argument is not supplied, then the search volume is
set to
$$\gamma_i(w) = \gamma_i w^q_i.$$
The values of \(\gamma_i\) (the search volume at 1g) and \(q_i\) (the
allometric exponent of the search volume) are taken from the gamma
and
q
columns in the species parameter dataframe. If the gamma
column is not supplied in the species parameter dataframe, a default is
calculated by the get_gamma_default()
function. Note that only
for predators of size \(w = 1\) gram is the value of the species parameter
\(\gamma_i\) the same as the value of the search volume \(\gamma_i(w)\).
The maximum intake rate \(h_i(w)\) of an individual of species \(i\) and
weight \(w\) determines the feeding level, calculated with
getFeedingLevel()
. It is measured in grams/year.
If the intake_max
argument is not supplied, then the maximum intake
rate is set to $$h_i(w) = h_i w^{n_i}.$$
The values of \(h_i\) (the maximum intake rate of an individual of size 1
gram) and \(n_i\) (the allometric exponent for the intake rate) are taken
from the h
and n
columns in the species parameter dataframe. If
the h
column is not supplied in the species parameter dataframe, it is
calculated by the get_h_default()
function, using the f0
and
the k_vb
column, if they are supplied.
If \(h_i\) is set to Inf
, fish of species i will consume all encountered food.
The metabolic rate is subtracted from the energy income rate to calculate
the rate at which energy is available for growth and reproduction, see
getEReproAndGrowth()
. It is measured in grams/year.
If the metab
argument is not supplied, then for each species the
metabolic rate \(k(w)\) for an individual of size \(w\) is set to
$$k(w) = k_s w^p + k w,$$
where \(k_s w^p\) represents the rate of standard metabolism and \(k w\)
is the rate at which energy is expended on activity and movement. The values
of \(k_s\), \(p\) and \(k\) are taken from the ks
, p
and
k
columns in the species parameter dataframe. If any of these
parameters are not supplied, the defaults are \(k = 0\), \(p = n\) and
$$k_s = f_c h \alpha w_{mat}^{n-p},$$
where \(f_c\) is the critical feeding level taken from the fc
column
in the species parameter data frame. If the critical feeding level is not
specified, a default of \(f_c = 0.2\) is used.
The external mortality is all the mortality that is not due to fishing or predation by predators included in the model. The external mortality could be due to predation by predators that are not explicitly included in the model (e.g. mammals or seabirds) or due to other causes like illness. It is a rate with units 1/year.
The ext_mort
argument allows you to specify an external mortality rate
that depends on species and body size. You can see an example of this in
the Examples section of the help page for setExtMort()
.
If the ext_mort
argument is not supplied, then the external mortality
is assumed to depend only on the species, not on the
size of the individual: \(\mu_{ext.i}(w) = z_{0.i}\). The value of the
constant \(z_0\) for each species is taken from the z0
column of the
species parameter data frame, if that column exists. Otherwise it is calculated
as
$$z_{0.i} = {\tt z0pre}_i\, w_{inf}^{\tt z0exp}.$$
For each species and at each size, the proportion \(\psi\) of the
available energy
that is invested into reproduction is the product of two factors: the
proportion maturity
of individuals that are mature and the proportion
repro_prop
of the energy available to a mature individual that is
invested into reproduction.
If the the proportion of individuals that are mature is not supplied via
the maturity
argument , then it is set to a sigmoidal
maturity ogive that changes from 0 to 1 at around the maturity size:
$${\tt maturity}(w) = \left[1+\left(\frac{w}{w_{mat}}\right)^{-U}\right]^{-1}.$$
(To avoid clutter, we are not showing the species index in the equations,
although each species has its own maturity ogive.)
The maturity weights are taken from the w_mat
column of the
species_params data frame. Any missing maturity weights are set to 1/4 of the
asymptotic weight in the w_inf
column.
The exponent \(U\) determines the steepness of the maturity ogive. By
default it is chosen as \(U = 10\), however this can be overridden by
including a column w_mat25
in the species parameter dataframe that
specifies the weight at which 25% of individuals are mature, which sets
\(U = \log(3) / \log(w_{mat} / w_{25}).\)
The sigmoidal function given above would strictly reach 1 only asymptotically.
Mizer instead sets the function equal to 1 already at the species'
maximum size, taken from the compulsory w_inf
column in the
species parameter data frame. Also, for computational simplicity, any
proportion smaller than 1e-8
is set to 0
.
If the the energy available to a mature individual that is
invested into reproduction is not supplied via the repro_prop
argument,
it is set to the allometric form
$${\tt repro\_prop}(w) = \left(\frac{w}{w_{inf}}\right)^{m-n}.$$
Here \(n\) is the scaling exponent of the energy income rate. Hence
the exponent \(m\) determines the scaling of the investment into
reproduction for mature individuals. By default it is chosen to be
\(m = 1\) so that the rate at which energy is invested into reproduction
scales linearly with the size. This default can be overridden by including a
column m
in the species parameter dataframe. The asymptotic sizes
are taken from the compulsory w_inf
column in the species parameter
data frame.
The total proportion of energy invested into reproduction of an individual of size \(w\) is then $$\psi(w) = {\tt maturity}(w){\tt repro\_prop}(w)$$
The reproductive efficiency \(\epsilon\), i.e., the proportion of energy allocated to
reproduction that results in egg biomass, is set through the erepro
column in the species_params data frame. If that is not provided, the default
is set to 1 (which you will want to override). The offspring biomass divided
by the egg biomass gives the rate of egg production, returned by
getRDI()
:
$$R_{di} = \frac{\epsilon}{2 w_{min}} \int N(w) E_r(w) \psi(w) \, dw$$
The stock-recruitment relationship is an emergent phenomenon in mizer, with several sources of density dependence. Firstly, the amount of energy invested into reproduction depends on the energy income of the spawners, which is density-dependent due to competition for prey. Secondly, the proportion of larvae that grow up to recruitment size depends on the larval mortality, which depends on the density of predators, and on larval growth rate, which depends on density of prey.
Finally, to encode all the density dependence in the stock-recruitment
relationship that is not already included in the other two sources of density
dependence, mizer puts the the density-independent rate of egg production
through a density-dependence function. The result is returned by
getRDD()
. The name of the density-dependence function is
specified by the RDD
argument. The default is the Beverton-Holt
function BevertonHoltRDD()
, which requires an R_max
column
in the species_params data frame giving the maximum egg production rate. If
this column does not exist, it is initialised to Inf
, leading to no
density-dependence. Other functions provided by mizer are
RickerRDD()
and SheperdRDD()
and you can easily use
these as models for writing your own functions.
Gears
In mizer
, fishing mortality is imposed on species by fishing gears. The
total per-capita fishing mortality (1/year) is obtained by summing over the
mortality from all gears,
$$\mu_{f.i}(w) = \sum_g F_{g,i}(w),$$
where the fishing mortality \(F_{g,i}(w)\) imposed by gear \(g\) on
species \(i\) at size \(w\) is calculated as:
$$F_{g,i}(w) = S_{g,i}(w) Q_{g,i} E_{g},$$
where \(S\) is the selectivity by species, gear and size, \(Q\) is the
catchability by species and gear and \(E\) is the fishing effort by gear.
Selectivity
The selectivity at size of each gear for each species is saved as a three
dimensional array (gear x species x size). Each entry has a range between 0
(that gear is not selecting that species at that size) to 1 (that gear is
selecting all individuals of that species of that size). This three
dimensional array can be specified explicitly via the selectivity
argument, but usually mizer calculates it from the gear_params
slot of
the MizerParams object.
To allow the calculation of the selectivity
array, the gear_params
slot
must be a data frame with one row for each gear-species combination. So if
for example a gear can select three species, then that gear contributes three
rows to the gear_params
data frame, one for each species it can select. The
data frame must have columns gear
, holding the name of the gear, species
,
holding the name of the species, and sel_func
, holding the name of the
function that calculates the selectivity curve. Some selectivity functions
are included in the package: knife_edge()
, sigmoid_length()
,
double_sigmoid_length()
, and sigmoid_weight()
.
Users are able to write their own size-based selectivity function. The first
argument to the function must be w
and the function must return a vector of
the selectivity (between 0 and 1) at size.
Each selectivity function may have parameters. Values for these
parameters must be included as columns in the gear parameters data.frame.
The names of the columns must exactly match the names of the corresponding
arguments of the selectivity function. For example, the default selectivity
function is knife_edge()
that a has sudden change of selectivity from 0 to 1
at a certain size. In its help page you can see that the knife_edge()
function has arguments w
and knife_edge_size
. The first argument, w
, is
size (the function calculates selectivity at size). All selectivity functions
must have w
as the first argument. The values for the other arguments must
be found in the gear parameters data.frame. So for the knife_edge()
function there should be a knife_edge_size
column. Because knife_edge()
is the default selectivity function, the knife_edge_size
argument has a
default value = w_mat
.
In case each species is only selected by one gear, the columns of the
gear_params
data frame can alternatively be provided as columns of the
species_params
data frame, if this is more convenient for the user to set
up. Mizer will then copy these columns over to create the gear_params
data
frame when it creates the MizerParams object. However changing these columns
in the species parameter data frame later will not update the gear_params
data frame.
Catchability
Catchability is used as an additional factor to make the link between gear selectivity, fishing effort and fishing mortality. For example, it can be set so that an effort of 1 gives a desired fishing mortality. In this way effort can then be specified relative to a 'base effort', e.g. the effort in a particular year.
Catchability is stored as a two dimensional array (gear x species). This can
either be provided explicitly via the catchability
argument, or the
information can be provided via a catchability
column in the gear_params
data frame.
In the case where each species is selected by only a single gear, the
catchability
column can also be provided in the species_params
data
frame. Mizer will then copy this over to the gear_params
data frame when
the MizerParams object is created.
Effort
The initial fishing effort is stored in the MizerParams
object. If it is
not supplied, it is set to zero. The initial effort can be overruled when
the simulation is run with project()
, where it is also possible to specify
an effort that varies through time.
By default, mizer uses a semichemostat model to describe the resource
dynamics in each size class independently. This semichemostat dynamics is implemented
by the function resource_semichemostat()
. You can change the
resource dynamics by writing your own function, modelled on
resource_semichemostat()
, and then passing the name of your
function in the resource_dynamics
argument.
The resource_rate
argument is a vector specifying the intrinsic resource
growth rate for each size class. If it is not supplied, then the intrinsic growth
rate \(r(w)\) at size \(w\)
is set to $$r(w) = r_{pp}\, w^{n-1}.$$
The values of \(r_{pp}\) and \(n\) are taken from the r_pp
and n
arguments.
The resource_capacity
argument is a vector specifying the intrinsic resource
carrying capacity for each size class. If it is not supplied, then the
intrinsic carrying capacity \(c(w)\) at size \(w\)
is set to $$c(w) = \kappa\, w^{-\lambda}$$
for all \(w\) less than w_pp_cutoff
and zero for larger sizes.
The values of \(\kappa\) and \(\lambda\) are taken from the kappa
and lambda
arguments.
If you are not happy with the assumptions that mizer makes by default about
the shape of the model functions, for example if you want to change one of
the allometric scaling assumptions, you can do this by providing your
choice as an array in the appropriate argument to setParams()
. The
sections below discuss all the model functions that you can change this way.
Because of the way the R language works, setParams
does not make the
changes to the params
object that you pass to it but instead returns a new
params object. So to affect the change you call the function in the form
params <- setParams(params, ...)
.
Usually, if you are happy with the way mizer calculates its model functions
from the species parameters and only want to change the values of some
species parameters, you would make those changes in the species_params
data
frame contained in the params
object using species_params<-()
.
Here is an example which assumes that
you have have a MizerParams object params
in which you just want to change
the gamma
parameter of the third species:
species_params(params)$gamma[[3]] <- 1000
Internally that will actually call setParams()
to recalculate any of the
other parameters that are affected by the change in the species parameter.
setParams()
will use the species parameters in the params
object to
recalculate the values of all the model functions except those for which you have set custom
values.
Other functions for setting parameters:
gear_params()
,
resource_params()
,
setExtMort()
,
setFishing()
,
setInitialValues()
,
setInteraction()
,
setMaxIntakeRate()
,
setMetabolicRate()
,
setPredKernel()
,
setReproduction()
,
setResource()
,
setSearchVolume()
,
species_params()