Leslie matrix models, named after Patrick Leslie who first introduced them in the 1940s, are a type of matrix population model (MPM) used to describe demography of age structured populations. They are commonly used in studies of wildlife, conservation and evolutionary biology.
In a Leslie MPM the square matrix is used to model discrete, age-structured population growth with a projection interval, typically representing years, as a time step. Each element in the matrix represents a transition probability between different age classes, or indicates the fertility of the age class. The information in the MPM can be split into two submatrices, representing survival/growth and reproduction (the fertility vector), respectively.
Survival Probabilities: The subdiagonal (immediately below the main diagonal) of the MPM consists of survival probabilities. Each entry here shows the probability that an individual of one age class will survive to the next age class. These probabilities can be understood as an age trajectory of survival that can be modelled using a mathematical model describing how age-specific mortality changes with age.
Fertility: The first row of the MPM contains the reproductive rates of each age class. These entries indicate how many new individuals each age class can expect to produce in each projection interval.
All other entries in the MPM are typically zero, indicating that those transitions are impossible.
To project the population size and structure through time, the MPM is multiplied by a vector that represents the current population structure (number of individuals in each age class). This process results in a new vector that shows the predicted structure of the population in the next time step. This calculation can be iterated repeatedly to project population and structure through time.
Leslie matrices are useful for studying population dynamics under different scenarios, such as changes in survival rates, fecundity rates, or management strategies. They have been widely applied in both theoretical and applied ecology.
The purpose of this vignette is to illustrate how to simulate sets of Leslie MPMs based on known functional forms of mortality and fertility. There are several reasons why one would want to do this, including, but not limited to:
In the following sections, this document will:
Before beginning, users will need to load the required packages.
There are numerous published and well-used functional forms used to
describe how mortality risk (hazard) changes with age. The
model_mortality
function (and its synonym
model_survival
) handles 6 of these models: Gompertz,
Gompertz-Makeham, Weibull, Weibull-Makeham, Siler and Exponential.
In a nutshell:
These are illustrated below.
In addition to these functional forms of mortality, there are, of
course, functional forms that have been used to model fertility. The
model_fertility
function handles five types: logistic,
step, von Bertalanffy, Normal and Hadwiger.
Collectively, these mortality and fertility functions offer a large scope for modelling the variety of demographic trajectories apparent across the tree of life.
To obtain a trajectory of mortality, users can use the
model_mortality
function, which takes as input the
parameters of a specified mortality model. The output of this function
is a standard life table data.frame
including columns for
age (x
), age-specific hazard (hx
),
survivorship (lx
), age-specific probability of death and
survival (qx
and px
). By default, the life
table is truncated at the age when the survivorship function declines
below 0.01 (i.e. when only 1% of individuals in a cohort would remain
alive).
(lt1 <- model_mortality(params = c(b_0 = 0.1, b_1 = 0.2), model = "Gompertz"))
#> x hx lx qx px
#> 1 0 0.1000000 1.00000000 0.1051240 0.8948760
#> 2 1 0.1221403 0.89487598 0.1268617 0.8731383
#> 3 2 0.1491825 0.78135045 0.1526972 0.8473028
#> 4 3 0.1822119 0.66204041 0.1832179 0.8167821
#> 5 4 0.2225541 0.54074272 0.2190086 0.7809914
#> 6 5 0.2718282 0.42231542 0.2606027 0.7393973
#> 7 6 0.3320117 0.31225886 0.3084127 0.6915873
#> 8 7 0.4055200 0.21595427 0.3626343 0.6373657
#> 9 8 0.4953032 0.13764186 0.4231275 0.5768725
#> 10 9 0.6049647 0.07940180 0.4892807 0.5107193
#> 11 10 0.7389056 0.04055203 0.5598781 0.4401219
#> 12 11 0.9025013 0.01784784 0.6330059 0.3669941
It can be useful to explore the impact of parameters on the mortality
hazard (hx
) graphically, especially for users who are
unfamiliar with the chosen models.
ggplot(lt1, aes(x = x, y = hx)) +
geom_line() +
ggtitle("Gompertz mortality (b_0 = 0.1, b_1 = 0.2)")
The model_fertility
function is similar to the
model_mortality
function, as it has arguments for the type
of fertility model, and its parameters. However, the output of the
model_fertility
function is a vector of fertility values
rather than a data.frame
. This allows us to add a fertility
column (fert
) directly to the life table produced earlier,
as follows:
(lt1 <- lt1 |>
mutate(fert = model_fertility(
age = x, params = c(A = 3),
maturity = 3,
model = "step"
)))
#> x hx lx qx px fert
#> 1 0 0.1000000 1.00000000 0.1051240 0.8948760 0
#> 2 1 0.1221403 0.89487598 0.1268617 0.8731383 0
#> 3 2 0.1491825 0.78135045 0.1526972 0.8473028 0
#> 4 3 0.1822119 0.66204041 0.1832179 0.8167821 3
#> 5 4 0.2225541 0.54074272 0.2190086 0.7809914 3
#> 6 5 0.2718282 0.42231542 0.2606027 0.7393973 3
#> 7 6 0.3320117 0.31225886 0.3084127 0.6915873 3
#> 8 7 0.4055200 0.21595427 0.3626343 0.6373657 3
#> 9 8 0.4953032 0.13764186 0.4231275 0.5768725 3
#> 10 9 0.6049647 0.07940180 0.4892807 0.5107193 3
#> 11 10 0.7389056 0.04055203 0.5598781 0.4401219 3
#> 12 11 0.9025013 0.01784784 0.6330059 0.3669941 3
Again, it can be useful to plot the relevant data to visualise it.
Users can now turn these life tables, containing age-specific
survival and fertility trajectories, into Leslie matrices using the
make_leslie_mpm
function. These MPMs can be large or small
depending on the maximum life span of the population: as mentioned
above, the population is modelled until less than 1% of a cohort remains
alive.
make_leslie_mpm(lifetable = lt1)
#> [,1] [,2] [,3] [,4] [,5] [,6] [,7]
#> [1,] 0.000000 0.0000000 0.0000000 3.0000000 3.0000000 3.0000000 3.0000000
#> [2,] 0.894876 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [3,] 0.000000 0.8731383 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [4,] 0.000000 0.0000000 0.8473028 0.0000000 0.0000000 0.0000000 0.0000000
#> [5,] 0.000000 0.0000000 0.0000000 0.8167821 0.0000000 0.0000000 0.0000000
#> [6,] 0.000000 0.0000000 0.0000000 0.0000000 0.7809914 0.0000000 0.0000000
#> [7,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.7393973 0.0000000
#> [8,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.6915873
#> [9,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [10,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [11,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [12,] 0.000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [,8] [,9] [,10] [,11] [,12]
#> [1,] 3.0000000 3.0000000 3.0000000 3.0000000 3.0000000
#> [2,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [3,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [4,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [5,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [6,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [7,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [8,] 0.0000000 0.0000000 0.0000000 0.0000000 0.0000000
#> [9,] 0.6373657 0.0000000 0.0000000 0.0000000 0.0000000
#> [10,] 0.0000000 0.5768725 0.0000000 0.0000000 0.0000000
#> [11,] 0.0000000 0.0000000 0.5107193 0.0000000 0.0000000
#> [12,] 0.0000000 0.0000000 0.0000000 0.4401219 0.3669941
It is sometimes desirable to create large numbers of MPMs with
particular properties in order to test hypotheses. For Leslie MPMs, this
can be implemented in a straightforward way using the function
rand_leslie_set
. This function generates a set of Leslie
MPMs based on defined mortality and fertility models, and using model
parameters that are randomly drawn from specified distributions. For
example, users may wish to generate MPMs for Gompertz models to explore
how rate of senescence influences population dynamics.
Users must first set up a data frame describing the distribution from
which parameters will be drawn at random. The data frame has a number of
rows equal to the number of parameters in the model, and two values to
describe the distribution. In the case of a uniform distribution, these
are the minimum and maximum parameter values, respectively and with a
normal distribution they represent the mean and standard deviation. The
parameters must be entered in the order they appear in the model
equations (see ?model_mortality
).
For the Gompertz-Makeham model: \(h_x = b_0 \mathrm{e}^{b_1 x} + c\)
The output
argument defines the output as one of six
types (Type1
through Type6
). These outputs
include CompadreDB
objects or list
objects,
and the MPMs can be split into the component submatrices (U and F, where
the MPM, A = U + F). In the special case Type6
the outputs
are provided as a list
of life tables rather than MPMs. If
the output is set as a CompadreDB
object, the mortality and
fertility model parameters used to generate the MPM are included as
metadata.
The following example illustrates the production of 50 Leslie MPMs
output to a CompadreDB
object based on the Gompertz-Makeham
mortality model and a step fertility model with maturity beginning at
age 0. An optional argument, scale_output = TRUE
will scale
the fertility in the output MPMs to ensure that population growth rate
is lambda. The scaling algorithm is a simple scaling factor, by which
the fertility part of the MPM (the F submatrix) is multiplied to ensure
that population growth rate is 1, and yet the shape (but not the
magnitude) of the fertility trajectory is maintained. This should be
used with care: The desirability of such a manipulation strongly depends
on the use the MPMs are put to.
mortParams <- data.frame(
minVal = c(0, 0.01, 0.1),
maxVal = c(0.05, 0.15, 0.2)
)
fertParams <- data.frame(
minVal = 2,
maxVal = 10
)
maturityParam <- c(0, 0)
(myMatrices <- rand_leslie_set(
n_models = 50,
mortality_model = "GompertzMakeham",
fertility_model = "step",
mortality_params = mortParams,
fertility_params = fertParams,
fertility_maturity_params = maturityParam,
dist_type = "uniform",
output = "Type1"
))
#> A COM(P)ADRE database ('CompadreDB') object with ?? SPECIES and 50 MATRICES.
#>
#> # A tibble: 50 × 8
#> mat mortality_model b_0 b_1 C fertility_model A
#> <list> <chr> <dbl> <dbl> <dbl> <chr> <dbl>
#> 1 <CompdrMt> gompertzmakeham 0.0457 0.141 0.129 step 8.64
#> 2 <CompdrMt> gompertzmakeham 0.0321 0.0827 0.174 step 3.08
#> 3 <CompdrMt> gompertzmakeham 0.0328 0.109 0.146 step 7.75
#> 4 <CompdrMt> gompertzmakeham 0.0467 0.0458 0.146 step 9.52
#> 5 <CompdrMt> gompertzmakeham 0.0489 0.0264 0.147 step 6.48
#> 6 <CompdrMt> gompertzmakeham 0.0452 0.0294 0.199 step 9.57
#> 7 <CompdrMt> gompertzmakeham 0.00412 0.0820 0.139 step 9.25
#> 8 <CompdrMt> gompertzmakeham 0.0223 0.127 0.174 step 8.49
#> 9 <CompdrMt> gompertzmakeham 0.0194 0.106 0.100 step 8.66
#> 10 <CompdrMt> gompertzmakeham 0.000367 0.0391 0.191 step 6.89
#> # ℹ 40 more rows
#> # ℹ 1 more variable: fertility_scaling <dbl>
The function operates quite fast. For example, on an older MacBook (3.10GHz Intel with 4 cores), it takes 17 seconds to generate 5000 MPMs with the parameters mentioned above.
As an aid to assessing the simulation, users can produce a simple
summary of the MPMs using the summarise_mpms
function.
Note, though, that this only works with CompadreDB
outputs.
In this case, because we are working with Leslie MPMs, the dimension of
the MPMs is indicative of the maximum age reached by individuals in the
population.
summarise_mpms(myMatrices)
#> Summary of matrix dimension:
#> Min. 1st Qu. Median Mean 3rd Qu. Max.
#> 15.00 18.25 22.00 22.98 26.00 39.00
#> Summary of lambda values:
#> Min. 1st Qu. Median Mean 3rd Qu. Max.
#> 2.845 6.010 7.970 7.557 9.150 10.672
#>
#> Summary of maximum F values:
#> Min. 1st Qu. Median Mean 3rd Qu. Max.
#> 2.002 5.157 7.142 6.720 8.327 9.788
#>
#> Summary of maximum U values:
#> Min. 1st Qu. Median Mean 3rd Qu. Max.
#> 0.7829 0.8159 0.8347 0.8365 0.8545 0.8925
#>
#> Summary of minimum non-zero U values:
#> Min. 1st Qu. Median Mean 3rd Qu. Max.
#> 0.5715 0.6881 0.7650 0.7514 0.8160 0.8814
After producing the output as a CompadreDB
object, the
matrices can be accessed using functions from the RCompadre
R package. For example, to get the A matrix, or the U/F submatrices
users can use the matA
, matU
or
matF
functions. The following code illustrates how to
rapidly calculate population growth rate for all of the matrices.
# Obtain the matrices
x <- matA(myMatrices)
# Calculate lambda for each matrix
sapply(x, popdemo::eigs, what = "lambda")
#> [1] 9.480062 3.889616 8.587381 10.343567 7.303660 10.356146 10.112353
#> [8] 9.308862 9.549256 7.720332 10.672096 7.928430 5.604869 8.872518
#> [15] 6.966830 7.339943 9.468459 3.993036 8.631979 2.871674 8.012464
#> [22] 3.567593 2.844529 8.688251 7.778629 5.968972 8.664013 9.523154
#> [29] 7.123514 9.482587 7.556071 10.495633 7.644149 7.441366 7.792883
#> [36] 9.092281 10.412818 5.422186 9.018497 8.325535 4.386485 5.377892
#> [43] 6.131147 3.940014 8.952296 4.907484 9.138780 9.154187 3.317446
#> [50] 8.668165
Users can examine the vignettes for the Rcompadre
and
Rage
packages for additional insight into other potential
operations with the compadreDB
object.
This vignette, has demonstrated the process of generating sets of Leslie matrices using functional forms of mortality and fertility. By following the steps outlined, users can simulate complex population dynamics scenarios, explore the influence of different parameters on demographic trajectories, and produce matrices for various applications, from theoretical studies to practical teaching tools.
The vignette started by introducing Leslie matrix models and their significance in studying age-structured population dynamics comprehensively. It then detailed the functional forms of mortality and fertility, providing examples of how to model these vital rates. Using these models, it showed how to create life tables that form the basis for constructing Leslie matrices.
The vignette also demonstrated how to produce multiple Leslie
matrices with specific properties using the rand_leslie_set
function. This allows for the generation of large datasets necessary for
hypothesis testing and various other advanced analyses. Additionally,
the vignette highlighted methods to summarise the simulated
matrices.
Overall, this vignette serves as a comprehensive guide for researchers and educators looking to employ Leslie matrix models in their work, providing the tools and knowledge needed to simulate and study population dynamics effectively.