Type: | Package |
Title: | Ecological Drift under the UNTB |
Version: | 1.7-7-1 |
Depends: | R (≥ 2.10) |
SystemRequirements: | PARI/GP >= 2.3.0 [strongly recommended for logkda()] |
Imports: | Brobdingnag (≥ 1.1-8), partitions (≥ 1.9-14), polynom |
Maintainer: | Robin K. S. Hankin <hankin.robin@gmail.com> |
Description: | Hubbell's Unified Neutral Theory of Biodiversity. |
License: | GPL-2 | GPL-3 [expanded from: GPL] |
URL: | https://github.com/RobinHankin/untb, https://robinhankin.github.io/untb/ |
BugReports: | https://github.com/RobinHankin/untb/issues |
Suggests: | testthat (≥ 3.0.0), vdiffr |
Config/testthat/edition: | 3 |
NeedsCompilation: | no |
Packaged: | 2024-09-11 10:39:13 UTC; rhankin |
Author: | Robin K. S. Hankin
|
Repository: | CRAN |
Date/Publication: | 2024-09-11 13:00:02 UTC |
Unified neutral theory of biodiversity
Description
Numerical simulations, and visualizations, of the unified neutral theory of biodiversity
Details
Package untb
uses two classes of object to represent an
ecosystem: class count
and class census
. In essence, a
count
object is a table of species abundances and a census
object is a list of individuals. See ?census
and ?count
for more details. Although objects of either class can be coerced to
the other, class count
is the preferred form: it is a more
compact representation, especially for large ecosystems.
The package simulates neutral ecological drift using function
untb()
. Function display.untb()
displays a semi-animated
graphic of an ecosystem undergoing neutral drift.
Author(s)
Robin K. S. Hankin
Maintainer: <hankin.robin@gmail.com>
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
R. K. S. Hankin 2007. Introducing untb, an R package for simulating ecological drift under the unified neutral theory of biodiversity. Journal of Statistical Software, volume 22, issue 12
Examples
a <- untb(start=rep(1,100),prob=0.005,gens=5000,keep=FALSE)
preston(a)
no.of.spp(a)
display.untb(start=rep(1,100),prob=0.1,gens=1000)
data(butterflies)
plot(butterflies,uncertainty=TRUE)
Add two count objects
Description
Adds two count objects
Usage
## S3 method for class 'count'
a + b
## S3 method for class 'census'
a + b
Arguments
a , b |
objects of class |
Details
Consider count objects a
and b
. Then a+b
is a
count object that records the number of each species in a
and
b
combined. It is as though the organisms in the surveys were
pooled.
Census objects are coerced to count objects, added, then the result coerced to a count object.
The operation is commutative and associative.
Author(s)
Robin K. S. Hankin, based on an R-help tip from Gabor Grothendiek
Examples
a <- count(c(dogs=4,pigs=0,slugs=5))
b <- count(c(slugs=4,hogs=1,frogs=19))
a+b
Various functions from Alonso and McKane 2004
Description
Various functions from Alonso and McKane 2004 dealing with analytical solutions of a neutral model of biodiversity
Usage
alonso.eqn6(JM, n, theta)
alonso.eqn11(J, n, theta)
alonso.eqn12(J, n, theta, give=FALSE)
Arguments
J , JM |
Size of the community and metacommunity respectively |
n |
Abundance |
theta |
Biodiversity constant |
give |
In function |
Details
Notation follows that of Alonso and McKane 2004
Note
Function alonso.eqn6()
is identical to function
vallade.eqn5()
Author(s)
Robin K. S. Hankin
References
D. Alonso and A. J. McKane 2004. “Sampling Hubbell's neutral model of biodiversity”, Ecology Letters 7:901-910
Examples
J <- 100
plot(1:J , alonso.eqn11(J,n=1:J,
theta=5),log="y",type="l",xlab="n",ylab=expression(S(n)),main="Eqns
11 and 12 of Alonso and McKane")
points(1:J , alonso.eqn12(J,n=1:J, theta=5),type="l",lty=2)
legend("topright",legend=c("equation 11","equation 12"),lty=1:2)
Barro Colorado Island (BCI) dataset
Description
The BCI dataset contains location and species identity for all 10cm dbh (diameter at breast height) trees on Barro Colorado Island, currently for years 1981-1983, 1985, 1990, 1995, 2000, and 2005. The subset of interest here is the abundances for each of the 252 species recorded.
The BCI dataset is not included in the untb package, because its licence appears to be inconsistent with the GPL.
It is discussed here because it was used as an example dataset in Hankin 2007.
Source
http://www.stri.org/english/research/facilities/terrestrial/barro_colorado/index.php
References
R. Condit, S. P. Hubbell and R. B. Foster 2005. Barro Colorado Forest Census Plot Data
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
R. K. S. Hankin 2007. “Introducing untb, an R package for simulating ecological drift under the unified neutral theory of biodiversity”. Journal of Statistical Software, volume 22, issue 12
abundance data for butterflies
Description
A dataset of class “count” showing the abundance of several butterfly species
Usage
data(butterflies)
Format
A table with names of different butterfly species, and entries corresponding to the respective numbers of individuals.
References
Texas Birding and Naturalist Web
Examples
data(butterflies)
plot(butterflies, uncertainty=TRUE)
Dataset due to Caruso
Description
A dataframe in standard format due to Migliorini and Caruso presenting observations of oribatid mites.
Usage
data(caruso)
Format
Dataset caruso
is a data frame with 194 observations on 5
variables. Each row corresponds to a species; the observations (rows)
are the species abundances in each of 5 habitats.
Following Migliorini et al 2002, the habitats were:
a pure beech woodland (‘
Beech
’)a coppice woodland (‘
Coppice
’)grassland (‘
Grassland
’)heathland (‘
Heathland
’)-
‘Biancana’ badlands (‘
Biancana
’)
Details
Oribatid mites are rather small and very interesting free living soil microarthropods. They have a huge species diversity with populations characterised by highly aggregated distributions over multiple spatial scales ranging from a few centimetres to hundreds of meters.
Within each habitat, several soil samples were collected (five randomly located replicates per each month: see the paper Migliorini et al. 2002). So, actually, that is a network of small samples that make a single large sample.
The five study areas of this data set belong to five habitats that are very typical of that Mediterranean region. These five areas also belong to a rather homogeneous biogeographical region (southern Tuscany). On the ground of what is known on the biology and community patterns of Oribatida, several a-priori hypotheses can be made on expected changes in the diversity of their assemblages and immigration rates respectively between and within the five areas. For instance, under the Neutral Model one might expect that the Beech forest should have the highest Theta and an immigration rate of about 1, while one might expect the opposite for the Biancana (a very arid habitat, a kind of gariga/garrigue with very patchy vegetation).
Note
Executing optimal.params.sloss(caruso)
does not return
useful output. The reason for this is unknown.
Source
Data kindly supplied by Tancredi Caruso
References
T. Caruso and others 2007. “The Berger-Parker index as an effective tool for monitoring the biodiversity of disturbed soils: a case study on Mediterranean oribatid (Acari: Oribatida) assemblages”. Biodiversity Conservation, 16:3277-3285
M. Migliorini, A. Petrioli, and F. Bernini 2002. “Comparative analysis of two edaphic zoocoenoses (Oribatid mites and Carabid beetles) in five habitats of the ‘Pietraporciana’ and ‘Lucciolabella’ Nature Reserves (Orcia Valley, central Italy)”. Acta Oecologica, 23:361-374
See Also
Examples
data(caruso)
summary(count(caruso[,1]))
Construct, coerce, and test for a census object
Description
In package untb, ecosystem data is held in one of two preferred forms:
census data and count data. Function as.census()
coerces to
census format.
Usage
census(a)
as.census(a)
is.census(a)
Arguments
a |
Ecosystem data. In function |
Details
A “census” object is a list of individuals in the form of an unnamed vector whose elements indicate the individuals' species; compare “count” objects.
An object of class “census” is also an unordered factor. The levels are always in alphabetical order.
Function census()
takes an object of class “count” and
returns an object of class “census”. This function is not
really intended for the end user.
Function as.census()
coerces to class “count” then
returns census()
of the result.
Value
Returns an object of class “census”.
Author(s)
Robin K. S. Hankin
See Also
Examples
jj <- c(dogs=4,pigs=10,slugs=0,fish=1)
x <- census(jj) # slugs appear as zero abundance
extant(x) # slugs gone
x+x # count method for census objects: order of elements lost
as.census(jj) # probably NOT what you meant
a <- c(rep("oak",5) ,rep("ash",2),rep("elm",3),rep("xx",4))
# note that "a" is a plain vector here.
as.census(a)
Copepod data supplied by Phil Pugh
Description
A dataset of copepod (resp: ostracod) abundances supplied by Dr Phil Pugh of the National Oceanography Centre, Southampton
Usage
data(copepod)
data(ostracod)
Format
A table with names of different copepod (resp: ostracod) species, and entries corresponding to the numbers of individuals of each species.
Source
Kindly supplied by Southampton Oceanography Centre.
Examples
data(copepod)
optimize(f=theta.likelihood,interval=c(10,100), maximum=TRUE,
S=no.of.spp(copepod), J=no.of.ind(copepod), give.log=TRUE)
data(ostracod)
preston(ostracod)
Construct, coerce, and test for a count object
Description
In package untb, ecosystem data is held in one of two preferred forms:
census data and count data. Function count
creates an object
of class “count”, and as.count()
coerces to this class.
Usage
as.count(a,add="")
count(a)
is.count(a)
Arguments
a |
Ecosystem data. In function |
add |
In function |
Details
A “count” object is a list of species together with their abundance. It also has class “table”; compare “census” objects.
An object of class “count” is a table sorted from most to least abundant species. The singletons are thus tabulated last.
Function count()
takes a vector, the elements of which are
interpreted as abundances. If any of the elements are named, the
names are interpreted as species names (unnamed elements are given the
null name). If the vector is unnamed, then the species names are
upper case letters, with the first element being named
“A
”, the second “B
”, and so on; this
behaviour is inherited from as.table()
. Note that this means
that the species names are not necessarily in alphabetical order.
From version 1.6-9, zero elements are interpreted as zero abundance
species (ie extinct).
To access or change species names, use names()
and
names<-
respectively.
Function as.count()
coerces its argument to count form.
Value
Returns an object of class “count”.
Author(s)
Robin K. S. Hankin
See Also
Examples
count(c(
slugs = 9, pigs = 1, dogs = 1, hogs = 2, bats = 3,
cats = 1, frogs = 1, pugs = 2, ants = 1,
yaks = 2, rats = 4))
a <- c(rep("oak",5) ,rep("ash",2),rep("elm",3),rep("xx",4))
as.count(a)
data(saunders)
as.count(saunders[1,-(1:150)])
jj <- sample(1:5,5,replace=TRUE)
as.count(jj)
as.count(jj,add="spp.")
Animation of neutral ecological drift
Description
Displays an ongoing simulation of neutral ecological drift using nice colours and a simple animation technique. Does not work as intended in RStudio: use base R
Usage
display.untb(start, gens=100, prob.of.mutate = 0, cex=3, individually
= TRUE, ask = FALSE, flash = FALSE, delay = 0, cols=NULL, ...)
Arguments
start |
Starting ecosystem; coerced to class census. Usually,
pass an object of class count; see examples. To start
with a monoculture of size 10, use |
gens |
Number of generations to simulate |
prob.of.mutate |
Probability of mutation. The default of zero
corresponds to |
cex |
The size of the dots used for plotting, defaulting to 3 |
individually |
Boolean, with default |
ask |
Boolean, with default |
flash |
Boolean, with |
delay |
Time delay between generations in seconds; meaningful
whatever the value of |
cols |
A vector of colours with default |
... |
Further arguments passed to |
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
Examples
data(butterflies)
display.untb(start=butterflies,prob=0, gens=1e2)
Etienne's sampling formula
Description
Function etienne()
returns the probability of a given dataset
given theta
and m
according to the Etienne's sampling
formula. Function optimal.params()
returns the maximum likelihood
estimates for theta
and m
using numerical optimization
Usage
etienne(theta, m, D, log.kda = NULL, give.log = TRUE, give.like = TRUE)
optimal.params(D, log.kda = NULL, start = NULL, give = FALSE, ...)
Arguments
theta |
Fundamental biodiversity parameter |
m |
Immigration probability |
D |
Dataset; a count object |
log.kda |
The KDA as defined in equation A11 of Etienne 2005. See details section |
give.log |
Boolean, with default |
give.like |
Boolean, with default |
start |
In function |
give |
In function |
... |
In function |
Details
Function etienne()
is just Etienne's formula 6:
P[D|\theta,m,J]=
\frac{J!}{\prod_{i=1}^Sn_i\prod_{j=1}^J{\Phi_j}!}
\frac{\theta^S}{(\theta)_J}\times
\sum_{A=S}^J\left(K(D,A)
\frac{(\theta)_J}{(\theta)_A}
\frac{I^A}{(I)_J}
\right)
where \log K(D,A)
is given by function logkda()
(qv). It
might be useful to know the (trivial) identity for the Pochhammer symbol
[written (z)_n
] documented in theta.prob.Rd
. For
convenience, Etienne's Function optimal.params()
uses
optim()
to return the maximum likelihood estimate for
\theta
and m
.
Compare function optimal.theta()
, which is restricted to no
dispersal limitation, ie m=1
.
Argument log.kda
is optional: this is the K(D,A)
as defined
in equation A11 of Etienne 2005; it is computationally expensive to
calculate. If it is supplied, the functions documented here will not
have to calculate it from scratch: this can save a considerable amount
of time
Author(s)
Robin K. S. Hankin
References
R. S. Etienne 2005. “A new sampling formula for biodiversity”. Ecology letters 8:253-260
See Also
Examples
data(butterflies)
## Not run: optimal.params(butterflies) #takes too long without PARI/GP
#Now the one from Etienne 2005, supplementary online info:
zoo <- count(c(pigs=1, dogs=1, cats=2, frogs=3, bats=5, slugs=8))
l <- logkda.R(zoo, use.brob=TRUE) # Use logkda() if pari/gp is available
optimal.params(zoo, log.kda=l) #compare his answer of 7.047958 and 0.22635923.
Expected abundances under the neutral model
Description
Returns a vector of expected abundances of the i-th ranked species under the neutral model
Usage
expected.abundance(J, theta)
Arguments
J |
Size of the ecosystem |
theta |
Biodiversity parameter |
Value
Returns an object of class count
. Species names (capital
letters) are assigned by function count()
.
Note
Function is very slow even for moderate J.
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
See Also
Examples
expected.abundance(J=10,theta=3)
sum(expected.abundance(J=10,theta=3)) #should be 10
Extract rows of a database in count form
Description
Extracts rows of a data frame and, if there is one row only, coerces to a count object, preserving the species names
Usage
extractor(x, index)
Arguments
x |
A data frame with column headings being species names |
index |
A vector of indices to extract |
Details
If index
is length one, the numbers are interpreted as species
counts, and the output is coerced to a count
object.
Author(s)
Robin K. S. Hankin
Examples
data(saunders)
plot(extant(extractor(saunders,1)))
Various functionality to implement Fisher's logseries
Description
Various functions connected to Fisher's logseries including creation of synthetic datasets and estimation of Fisher's alpha
Usage
fishers.alpha(N, S, give=FALSE)
fisher.ecosystem(N, S, nmax, alpha=NULL, c=0)
Arguments
N |
Size of the ecosystem. In the case of
|
S |
Number of species in ecosystem |
alpha |
In function |
give |
In function |
nmax |
In function |
c |
In function |
Details
Function fishers.alpha()
solves for \alpha
given
N
and S
, as per Fisher's table 9, p55.
Given N
and S
(or \alpha
), function
fisher.ecosystem()
generates a Fisherian ecosystem
with expected size N
and expected species count S
.
Author(s)
Robin K. S. Hankin
References
R. A. Fisher and A. S. Corbet and C. B. Williams 1943. “The relation between the number of species and the number of individuals in a random sample of an animal population”, Journal of Animal Ecology, volume 12, pp 42–58
Examples
fishers.alpha(N=100000,S=100)
#compare the Table value:
100000/10^3.95991
Tree counts in 1-ha plots from the Western Ghats mountains (South India)
Description
Tree species counts are given in 50 one-hectare sampling plots (species by sample matrix). This only includes trees over 10 cm dbh (diameter at breast height) and species labels (row names) are numeric.
Usage
data(ghats)
Format
Data frame displaying 304 species counts over 50 one-hectare plots.
Source
Ecological Archives E088-149-A1. http://www.esapubs.org/Archive/ecol/E088/149/appendix-A.htm
References
Francois Munoz, Pierre Couteron, B. R. Ramesh, and Rampal S. Etienne 2007. “Estimating parameters of neutral communities: from one single large to several small samples.” Ecology 88(10):2482-2488.
Examples
data(ghats)
# Rank-abundance picture of plot 1 (column 1 in ghats)
plot(extant(count(ghats[,1])))
#histogram of optimal theta across the 50 plots:
hist(apply(ghats,2,optimal.theta),col='gray')
Randomly select a subset of an ecosystem
Description
Return an ecosystem comprised of individuals randomly sampled from a metacommunity
Usage
isolate(a, size = no.of.ind(a), replace = TRUE)
Arguments
a |
Ecosystem data |
size |
Number of individuals to sample |
replace |
Boolean, with default |
Details
Setting argument replace
to default TRUE
is much
faster.
The canonical example is given by Leigh et al 1993, in which islands were isolated from the mainland by rising waters. The trees on the islands were held to be a randomly drawn sample from the metacommunity.
Given that the usual usage of this function is to generate a plausible
ecosystem under such a scenario, one would have a hard time justifying
the use of replace=TRUE
as it allows (for example) a singleton
metacommunity species to have multiple representatives in the returned
ecosystem.
However, for large metacommunities and small subsamples, the distinction
between replace=TRUE
and replace=FALSE
is small.
Value
Returns a count
object
Note
If replace=FALSE
, the returned count object includes extinct
species. Use extant(isolate(...))
to return only extant species
Author(s)
Robin K. S. Hankin
References
E. G. Leigh and others 1993. “The decline of tree diversity on newly isolated tropical islands: a test of a null hypothesis and some implications”. Evolutionary Ecology, 7:76-102
Examples
a <- rand.neutral(1000,10)
no.of.spp(a)
no.of.spp(isolate(a))
logarithms of Stirling numbers of the first kind
Description
Natural logarithms of Stirling numbers of the first kind, used by
function logkda.a11()
(dataset logS1
) and function
logkda.polyn()
(dataset logS1vect
).
Usage
logS1
Format
Dataset logS1
is a 100-by-100 matrix of logs of Stirling numbers
of the first kind; logS1vect
is a vector of length 499500
Source
Calculated by Maple
See Also
Examples
exp(logS1[1:5,1:5])
Etienne's K(D,A)
Description
Calculates Etienne's K(D,A)
using a variety of different methods
Usage
logkda.R(a, use.brob=TRUE)
logkda.a11(a)
logkda.pari(a, numerical=TRUE, gp_binary = "gp")
logkda.polyn(a)
logkda(a, method="pari", ...)
logkda_pari_unix(a, numerical, pari_string, gp_binary)
logkda_pari_windows(a, numerical, pari_string)
Arguments
a |
Count object |
use.brob |
In function |
numerical |
Boolean, with default |
method |
In function |
pari_string , gp_binary |
configuration variables (not intended to be changed by the user) |
... |
In function |
Details
The user should use function logkda()
, which is a wrapper for
the other functions. Note that the default method, pari
,
requires the pari/gp system to be installed. This is the preferred
option because it is much faster than the other methods.
Functions logkda.R()
and logkda.pari()
calculate
K(D,A)
using the method appearing in Etienne (2005), supplementary
online material; they use R
and pari/gp
respectively.
Function logkda.a11
is a direct implementation of formula A11
in Etienne (2005). The formula is
K(D,A)=
\sum_{\left\{a_1,\ldots,a_S|\sum a_i=A\right\}}
\prod_{i=1}^S\frac{
\overline{s}\left(n_i, a_i\right)
\overline{s}\left(a_i, 1\right) }{
\overline{s}\left(n_i,1\right)}
where \overline{s}\left(n_i,a_i\right)
are Stirling numbers of
the first kind (see logS1
).
Function logkda.pari()
dispatches to either
logkda_pari_unix()
or logkda_pari_windows()
but the
windows function is not guaranteed to work.
Note
If method
takes its default value of “pari
”, and
pari/gp
is not installed (the test is gp --version
),
then the method is changed to R
and a warning given.
Function logkda.a11()
is included because the computational
method is a direct transcription of formula A11; it is very slow.
Function logkda.pari()
is a wrapper for
.logkda.pari.windows()
or .logkda.pari.unix()
. It uses
“if(R.Version()$os == 'windows')
” to check for windows
operating systems.
It would be nice to use gp2c
(rather than gp
) but I
can't make the “-g
” flag work properly; and I had to
hack gp2c-run
to make it call gp
with the -q
flag
Author(s)
Robin K. S. Hankin; logkda()
is an R transliteration of
pari/gp
code appearing in Etienne 2005 (supplementary online
material) due to Chave.
Function logkda.polyn()
provided by Francois Munoz.
Function .logkda.pari.windows()
provided by Andrea Manica and
Francois Munoz.
References
R. S. Etienne 2005. “A New Sampling Formula for Neutral
Biodiversity”. Ecology Letters, volume 8, pp253–260.
doi: 10.111/j.1461-0248.2004.00717.x
C. Batut and K. Belabas and D. Bernardi and H. Cohen and M. Olivier 2000. “User's guide to PARI/GP”. http://www.parigp-home.de/
See Also
Examples
a <- count(c(dogs=7,pigs=3,crabs=1,hogs=1,slugs=1))
## Not run: logkda(a)
logkda.R(a)
logkda.R(a, use.brob=FALSE)
logkda.a11(a)
# All four should be the same up to numerical errors
Ecosystem diagnostics
Description
Ecosystem diagnostics such as species count, individual count, number of singletons, etc
Usage
no.of.ind(x)
no.of.spp(x, include.extinct=FALSE)
no.of.singletons(x)
no.of.extinct(x)
maximal.abundance(x)
singletons(x)
extinct(x)
extant(x)
Arguments
x |
Ecosystem vector; is coerced to class |
include.extinct |
In function |
Details
-
Function
no.of.spp()
returns the number of species in an ecosystem object, treating extinct species in line with argumentinclude.extinct
-
Function
no.of.ind()
returns the number of individuals -
Function
no.of.singletons()
returns the number of singletons -
Function
no.of.extinct()
returns the number of extinct species -
Function
maximal.abundance()
returns the abundance of the most abundant species -
Function
singletons()
returns acount
object containing only the singletons: each abundance is one -
Function
extinct()
returns acount
object containing only the extinct species: each abundance is zero -
Function
extant()
returns acount
object containing only the extant species: each abundance is greater than zero
Note
It is sometimes useful to include species with an abundance of zero when, for example, taking a single row of the Saunders dataframe.
The default for include.extinct
is FALSE
because this is
required for (eg) optimal.theta()
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell. “The Unified Neutral Theory of Biodiversity”. Princeton University Press, 2001.
Examples
data(butterflies)
no.of.spp(butterflies)
no.of.ind(butterflies)
jj1 <- count(c(dogs=7,pigs=3,crabs=0,slugs=1))
jj2 <- count(c(squid=0,dogs=3,bugs=0))
jj3 <- count(c(bugs=3,rats=0,crabs=3,cats=0))
extinct(jj1 + jj2)
extinct(jj3) #rats and cats
extant(jj3) #bugs and crabs
singletons(jj1)
singletons(jj2) # empty
singletons(jj1 + jj3) # slugs
Estimation of local immigration using GST(k) statistics
Description
Functions optimal.params.gst()
, GST.k()
and I.k()
apply to count data collected over a network of community samples k
(species by sample matrix). A theoretical relationship between
GST(k)
statistics and local immigration numbers I(k)
, in
the context of a spatially-implicit neutral community model (Munoz et
al 2008), is used to provide GST(k)
and I(k)
statistics
any sample k.
If requested, optimal.params.gst()
further provides the user with
confidence bounds.
Usage
optimal.params.gst(D, exact = TRUE, ci = FALSE, cint = c(0.025, 0.975), nbres = 100)
GST.k(D, exact = TRUE)
I.k(D, exact = TRUE)
Arguments
D |
A data table including species counts in a network of community samples (columns) |
exact |
If |
ci |
Specifies whether bootstraps confidence intervals of immigration estimates are to be calculated |
cint |
Bounds of the confidence interval, if |
nbres |
Number of rounds of the bootstrap procedure for confidence interval calculation, if ci = T |
Value
GST |
A vector of 0 to 1 |
nk |
Number of individuals within samples (length = number of samples) |
distrib |
Species counts of the merged dataset (output of |
I |
Immigration estimates (output of |
m |
Corresponding immigration rates (output of |
Ici |
Confidence interval of |
mci |
Confidence interval of |
Iboot |
Table of bootstrapped values of |
mboot |
Table of bootstrapped values of i |
Author(s)
Francois Munoz
References
Francois Munoz, Pierre Couteron and B.R. Ramesh (2008). “Beta-diversity in spatially implicit neutral models: a new way to assess species migration.” The American Naturalist 172(1): 116-127
See Also
optimal.params
,optimal.params.sloss
Examples
data(ghats)
optimal.params.gst(ghats)
Estimation of neutral community parameters using a two-stage maximum-likelihood procedure
Description
Function optimal.params.sloss()
returns maximum likelihood
estimates of theta
and m(k)
using numerical
optimization.
It differs from untb
's optimal.params()
function as it
applies to a network of smaller community samples k
instead of
to a single large community sample.
Although there is a single, common theta
for all communities,
immigration estimates are provided for each local community k
,
sharing a same biogeographical background.
Usage
optimal.params.sloss(D, nbres = 100, ci = FALSE, cint = c(0.025, 0.975))
Arguments
D |
Species counts over a network of community samples (species by sample table) |
nbres |
Number of resampling rounds for |
ci |
Specifies whether bootstraps confidence intervals should be provided for estimates |
cint |
Bounds of confidence intervals, if ci = T |
Value
theta |
Mean |
I |
The vector of estimated immigration numbers |
Output of the bootstrap procedure, if ci = T:
thetaci |
Confidence interval for |
msampleci |
Confidence intervals for |
thetasamp |
theta estimates provided by the resampling procedure |
Iboot |
Bootstrapped values of |
mboot |
Bootstrapped values of |
Note
The function returns unhelpful output when run with the
caruso
dataset as in optimal.params.sloss(caruso)
. The
reason for this behaviour is unknown.
Author(s)
Francois Munoz
References
Francois Munoz, Pierre Couteron, B. R. Ramesh, and Rampal S. Etienne 2007. “Estimating parameters of neutral communities: from one single large to several small samples”. Ecology 88(10):2482-2488
See Also
optimal.params, optimal.params.gst
Examples
data(ghats)
optimal.params.sloss(ghats)
Returns an estimate of the fundamental biodiversity number
Description
Returns a maximum likelihood estimate for the fundamental biodiversity
number \theta
(function optimal.theta()
) or the
probability of mutation (function optimal.prob()
) and optionally
return information about the likely error
Usage
optimal.prob(x, interval=NULL, N=NULL, like=NULL, ...)
optimal.theta(x, interval=NULL, N=NULL, like=NULL, ...)
Arguments
x |
Ecosystem vector or species count table |
interval |
Bracketing interval for probability of mutation to be
passed to the optimization routine (here |
N |
Integer; the number of parametric resampled estimates to
give. Default of |
like |
Units of likelihood to calculate credible interval. Edwards recommends using 2 |
... |
Further arguments passed to |
Note
The fundamental biodiversity parameter \theta
is
2\nu J
, where \nu
is the probability of
mutation (ie, as estimated by optimal.prob()
), and J
is
the size of the ecosystem.
For the general case of dispersal limitation, see functions
etienne()
and optimal.params()
.
Author(s)
Robin K. S. Hankin
See Also
etienne
,optimal.params.sloss
,optimal.params.gst
Examples
data(butterflies)
optimal.prob(butterflies)
optimal.theta(butterflies)
Hubbell's phi
Description
Hubbell's phi: counts of species abundances
Usage
phi(x,addnames=TRUE)
unphi(freq, string="spp")
Arguments
x |
Ecosystem vector; is coerced to class |
addnames |
Boolean with default
|
freq |
Frequency data (eg as returned by |
string |
Character; species name to prepend (using |
Details
Function phi()
coerces its argument to a count
object and
by default returns a named vector whose i
th element is the
number of species with i
individuals. The name of the
i
th element is the species with abundance i
if unique
and empty otherwise. Function phi()
is used by
theta.prob()
.
Function unphi()
does the reverse: given the output of
phi()
, it returns a corresponding count
object. Note that
species names are lost.
Note
The code for setting the names is a dog's breakfast
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
See Also
Examples
jj <- c(rep("oak",5) ,rep("ash",2),rep("elm",3),"pine","tea","yew")
a <- as.count(jj)
phi(a)
unphi(phi(a)) #should match 'a' except for species names (which are lost)
data(butterflies)
phi(butterflies,add=FALSE)
summary(unphi(phi(butterflies))) #should match 'summary(butterflies)'
Abundance curves
Description
Plot the ranked abundance curve
Usage
## S3 method for class 'count'
plot(x, uncertainty = FALSE, expectation = FALSE, theta = NULL, n = 10, ...)
## S3 method for class 'census'
plot(x, uncertainty = FALSE, expectation = FALSE, theta = NULL, n = 10, ...)
Arguments
x |
Ecosystem object, coerced to class count |
uncertainty |
Boolean,
with |
expectation |
Boolean,
with |
theta |
Fundamental biodiversity number used if argument
|
n |
Number of bootstrapped estimates to plot |
... |
Extra parameters passed to |
Details
Plots a ranked abundance curve, optionally with parametrically resampled datasets showing the uncertainties
Note
If using expectation
, it's usually necessary to set ylim
and possibly xlim
manually.
Author(s)
Robin K. S. Hankin
Examples
data(copepod)
plot(copepod)
data(butterflies)
plot(butterflies,uncertainty=TRUE)
x <- count(c(pigs=1, dogs=1, cats=2, frogs=3, bats=5, slugs=8))
plot(x,expectation=TRUE,ylim=c(0.5,10))
Preston diagram of an ecosystem
Description
Gives a standard Preston diagram for an ecosystem.
Usage
preston(x,n=NULL,original=FALSE)
Arguments
x |
Ecosystem vector that is coerced to class |
n |
An integer specifying the number of species abundance classes
to use, with default |
original |
Boolean, with default |
Details
The Preston diagram is a table showing the number of species having
abundances in specified abundance classes. Consider the following
Preston diagram, created with original = FALSE
:
1 2 3-4 5-8 9-16 17-32 33-64 65-Inf number of species 10 5 7 5 1 5 4 0
This shows that there are 10 species with abundance 1 (that is, singletons); 5 species with abundance 2; 7 species with abundance 3-4; 5 species with abundance 5-8, and so on. This method is used by Hubbell (2001), and Chisholm and Burgman (2004).
Setting argument original
to TRUE
means to follow Preston
(1948) and count any species with an abundance on the boundary between
two adjacent abundance classes as being split 50-50 between the classes.
Thus the fourth class would be
\phi_4/2+\phi_5+\phi_6+\phi_7+\phi_8/2
where \phi_i
is the number of species with abundance
i
(given by phi(x)
).
Value
Function preston()
returns an object of class “preston
”.
Author(s)
Robin K. S. Hankin
References
-
F. W. Preston 1948. “The Commonness, and Rarity, of Species”. Ecology 29(3):254-283
-
R. A. Chisholm and M. A. Burgman 2004. “The unified neutral theory of biodiversity and biogeography: comment”. Ecology 85(11): 3172-3174
-
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press
See Also
Examples
preston(untb(start=rep(1,100), prob=0.01, gens=1000, keep=FALSE))
data(butterflies)
preston(butterflies)
preston(butterflies,original=TRUE)
data(copepod)
preston(copepod)
plot(preston(copepod))
Print and plot objects of class Preston
Description
Print and plot objects of class Preston
Usage
## S3 method for class 'preston'
print(x, ...)
## S3 method for class 'preston'
plot(x, ...)
Arguments
x |
Object of class “preston” |
... |
further arguments passed to |
Note
Intended to work with the output of function preston()
.
See the vignette for how to annotate a Preston plot.
Author(s)
Robin K. S. Hankin
See Also
Examples
data(butterflies)
print(preston(butterflies))
Print method for summary objects
Description
Print method for summary objects
Usage
## S3 method for class 'summary.count'
print(x, ...)
Arguments
x |
Object of class “summary.count” |
... |
extra arguments, currently ignored |
Author(s)
Robin K. S. Hankin
Examples
data(butterflies)
summary(butterflies)
Random neutral ecosystem
Description
Given the size of the metacommunity J
, and the fundamental
biodiversity number \theta
, generate an object of class
count
using a stochastic mechanism consistent with the
neutral theory.
Usage
rand.neutral(J, theta=NULL, prob.of.mutate=NULL, string = NULL, pad = FALSE)
Arguments
J |
Size of metacommunity |
theta |
Fundamental biodiversity number |
prob.of.mutate |
Probability of mutation |
string |
String to add to species names. By default (ie
|
pad |
Boolean, with default |
Details
Uses the simulation method on page 289 of Hubbell (2001).
Note
If pad
is TRUE
, and you set string
to
“extinct
”, things will break.
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
See Also
Examples
rand.neutral(1000, 9)
rand.neutral(1000, 9, string="spp.")
data(butterflies)
rand.neutral(no.of.ind(butterflies), optimal.theta(butterflies),string="spp.")
# what is the distribution of abundance of the second ranked species if
# J=10, theta=0.7?
plot(table(replicate(100,rand.neutral(10,theta=0.7,pad=TRUE)[2])))
Biodiversity dataset provided by SAHFOS
Description
Species counts in the North Atlantic
Usage
data(sahfos)
References
Warner AJ and Hays GC 1994. “Sampling by the Continuous Plankton Recorder Survey”. Progress in Oceanography, 34: 237-256
Examples
data(sahfos)
preston(sahfos)
Dataset due to Saunders
Description
A dataframe showing species inventories for a kelp holdfast
(saunders
) including a Boolean flag indicating whether the
holdfast was in a sheltered or exposed location.
Also two data frames, one for the 20 exposed holdfasts
(saunders.exposed
) and one for the 20 sheltered holdfasts
(saunders.sheltered
).
Also three count
objects, giving counts for all organisms
(saunders.tot
), all those from exposed locations
(saunders.exposed.tot
), and all those from sheltered locations
only (saunders.sheltered.tot
).
Usage
data(saunders)
Format
Dataset saunders
is a dataframe with 40 observations on 177
variables. Each row corresponds to a holdfast. The first column is
Boolean, indicating whether or not that holdfast was exposed
(TRUE
) or sheltered (FALSE
). The other columns show
species abundances for each of 176 species.
Summary datasets saunders.sheltered.tot
,
saunders.exposed.tot
, and saunders.tot
are objects of
class count
that are the species abundance for sheltered
holdfasts, exposed holdfasts, and the entire dataset.
The user will probably be most interested in saunders.sheltered
and saunders.exposed
, which are the transpose of the
appropriate rows of saunders
. Thus these dataframes have 176
rows, one per species and 20 rows, one per holdfast.
Details
Kelp are large seaweeds classified in kingdom Chromista. Kelp grows in shallow oceans in kelp forests.
The holdfast is a root-like structure that anchors the kelp to the ocean floor. Fauna inhabiting kelp holdfasts, being “incredibly diverse” (Anderson et al 2005), are often used as indicators of environmental change.
The data was collected in New Zealand, from eight sites along the Leigh coastline from north of Leigh Harbour down to the southern end of Kawau Island (a stretch of roughly 20 km). Four sites were wave-exposed, four were sheltered (although two of the latter were arguably quite tidally-dominated). Each site had a spatial extent of roughly one hectare. They were collected from 5 - 10 November, 2003.
The saunders
dataset must be arranged as it is because if it
were transposed, the first row would be the (nonsensical) observation
c(T,T,...,T,F,...,F)
.
Note
It is not entirely obvious how to derive the summary datasets from the
saunders
dataframe. Use function extractor()
for this.
Source
Data supplied by Justine Saunders
References
J. Saunders 2007. “Biodiversity of kelp holdfasts” (provisional title). PhD thesis (in preparation); School of Geography and Environmental Sciences, The University of Auckland
M. J. Anderson and others 2005. “Consistency and variation in kelp holdfast assemblages: Spatial patterns of biodiversity for the major phyla at different taxonomic resolutions”. Journal of Experimental Marine Biology and Ecology. Volume 320, pages 35-56
See Also
Examples
data("saunders")
jj <- t(saunders)[-1,]
jj.exposed <- saunders[,1]
"saunders.tot" <- count(apply(jj,1,sum))
"saunders.exposed" <- jj[, jj.exposed]
"saunders.sheltered" <- jj[,!jj.exposed]
"saunders.exposed.tot" <- count(apply(saunders.exposed,1,sum))
"saunders.sheltered.tot" <- count(apply(saunders.sheltered,1,sum))
plot(saunders.sheltered.tot, uncertainty=TRUE, n=1)
preston(saunders.tot)
optimal.params.sloss(saunders.exposed)
Simpson's diversity index
Description
Simpson's diversity index
Usage
simpson(x, with.replacement=FALSE)
Arguments
x |
Ecosystem vector; coerced to class |
with.replacement |
Boolean, with default |
Details
Returns the Simpson index D
: the
probability that two randomly sampled individuals belong to
different species.
There is some confusion as to the precise definition: some authors specify that the two individuals are necessarily distinct (ie sampling without replacement), and some do not.
Simpson (1949) assumed sampling without replacement and gave
1-\frac{\sum_{i=1}^Sn_i\left(n_i-1\right)}{J(J-1)}
in our notation.
He and Hu (2005) assumed sampling with replacement:
1-\frac{\sum_{i=1}^Sn_i^2}{J^2}.
The difference is largely academic but is most pronounced when many species occur with low counts (ie close to 1).
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
F. He and X.-S. Hu 2005. “Hubbell's Fundamental Biodiversity Parameter and the Simpson Diversity Index”. Ecology Letters, volume 8, pp386-390. doi:
10.1111/j.1461-0248.2005.00729.x
E. H. Simpson 1949. “Measurement of diversity”, Nature, volume 163, p688
See Also
Examples
data(butterflies)
D <- simpson(butterflies)
theta <- optimal.prob(butterflies)*2*no.of.ind(butterflies)
# compare theta with D/(1-D) (should be roughly equal; see He & Hu 2005):
theta
D/(1-D)
# Second argument pedantic in practice.
# Mostly, the difference is small:
simpson(butterflies,FALSE) - simpson(butterflies,TRUE)
# Most extreme example:
x <- count(c(1,1))
simpson(x,TRUE)
simpson(x,FALSE)
Ecosystem diagnostics for output of untb()
Description
Provides ecosystem diagnostics of species count datasets (species
counts and species tables), useful for the output of untb()
Usage
species.count(x)
species.table(x)
Arguments
x |
An integer matrix whose rows are integers representing the individuals' species |
Details
These functions takes a matrix argument, which is interpreted as the
output of untb(...,keep=TRUE)
.
Function species.count()
returns the total number of species
present in each row (ie at each timestep).
Function species.table()
returns a matrix M
where
M[i,j]
column of the matrix is the abundance of species j
at time i
.
Author(s)
Robin K. S. Hankin
See Also
Examples
a <- untb(start=rep(1,50), prob=0.01, gens=2000, keep=TRUE)
plot(species.count(a),type="b")
matplot(species.table(a),type="l",lty=1)
jj <- a[2000,]
print(jj)
as.count(jj)
Counts of diatom species in springs of the Adamello-Brenta Nature Park
Description
A dataset due to Spitale and Cantonati comprising abundances of different species of diatoms
Usage
data(spitale)
Format
A count object
Source
Data kindly provided by Daniel Spitale
References
D. Spitale and M. Cantonati 2011. “Understanding the natural variability of diatom assemblages in springs of the Adamello-Brenta Nature Park (south-eastern Alps) on a temporal scale”. Fundamental Applied Limnology volume 179/2, pp137–149
Examples
data(spitale)
summary(spitale)
Summary methods for count and census objects
Description
Summary methods for count and census objects
Usage
## S3 method for class 'count'
summary(object, ...)
## S3 method for class 'census'
summary(object, ...)
Arguments
object |
Ecosystem object coerced to class count |
... |
Further arguments, currently ignored |
Details
Prints a summary of an ecosystem object.
Author(s)
Robin K. S. Hankin
See Also
Examples
data(ostracod)
summary(ostracod)
Posterior probabilities for theta
Description
Determines the posterior probability and likelihood for theta, given a count object
Usage
theta.prob(theta, x=NULL, give.log=TRUE)
theta.likelihood(theta, x=NULL, S=NULL, J=NULL, give.log=TRUE)
Arguments
theta |
biodiversity parameter |
x |
object of class count or census |
give.log |
Boolean, with |
S , J |
In function |
Details
The formula was originally given by Ewens (1972) and is shown on page 122 of Hubbell (2001):
\frac{J!\theta^S}{
1^{\phi_1}2^{\phi_2}\ldots J^{\phi_J}
\phi_1!\phi_2!\ldots \phi_J!
\prod_{k=1}^J\left(\theta+k-1\right)}.
The likelihood is thus given by
\frac{\theta^S}{\prod_{k=1}^J\left(\theta+k-1\right)}.
Etienne observes that the denominator is equivalent to a Pochhammer
symbol (\theta)_J
, so is thus readily evaluated as
\Gamma(\theta+J)/\Gamma(\theta)
(Abramowitz and Stegun 1965, equation 6.1.22).
Note
If estimating theta
, use theta.likelihood()
rather than
theta.probability()
because the former function generally
executes much faster: the latter calculates a factor that is
independent of theta
.
The likelihood function L(\theta)
is any function of
\theta
proportional, for fixed observation z
, to
the probability density f(z,\theta)
. There is thus
a slight notational inaccuracy in speaking of “the” likelihood
function which is defined only up to a multiplicative constant. Note
also that the “support” function is usually defined as a
likelihood function with maximum value 1
(at the maximum
likelihood estimator for \theta
). This is not easy to
determine analytically for J>5
.
Note that S
is a sufficient statistic for \theta
.
Function theta.prob()
does not give a PDF for
\theta
(so, for example, integrating over the real line
does not give unity). The PDF is over partitions of J
; an
example is given below.
Function theta.prob()
requires a count object (as opposed to
theta.likelihood()
, for which J
and S
are
sufficient) because it needs to call phi()
.
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”, Princeton University Press.
W. J. Ewens 1972. “The sampling theory of selectively neutral alleles”, Theoretical Population Biology, 3:87–112
M. Abramowitz and I. A. Stegun 1965. Handbook of Mathematical Functions, New York: Dover
See Also
Examples
theta.prob(1,rand.neutral(15,theta=2))
gg <- as.count(c(rep("a",10),rep("b",3),letters[5:9]))
theta.likelihood(theta=2,gg)
optimize(f=theta.likelihood,interval=c(0,100),maximum=TRUE,x=gg)
## An example showing that theta.prob() is indeed a PMF:
a <- count(c(dogs=3,pigs=3,hogs=2,crabs=1,bugs=1,bats=1))
x <- partitions::parts(no.of.ind(a))
f <- function(x){theta.prob(theta=1.123,extant(count(x)),give.log=FALSE)}
sum(apply(x,2,f)) ## should be one exactly.
Ecological drift simulation under the Unified Neutral Theory of Biodiversity
Description
Simulates ecological drift under the UNTB. Function untb()
carries out the simulation; function select()
carries out a single generational step.
Usage
untb(start, prob=0, D=1, gens=150, keep=FALSE, meta=NULL)
select(a, D=length(a), prob=0, meta=NULL)
select.mutate(a, D=length(a), prob.of.mutate=0)
select.immigrate(a, D=length(a), prob.of.immigrate=0, meta)
Arguments
a , start |
Starting ecosystem; coerced to class census. Usually,
pass an object of class count; see examples. To start
with a monoculture of size 10, use |
prob , prob.of.immigrate , prob.of.mutate |
Probability of “new” organism not being a descendent of an existing individual |
D |
Number of organisms that die in each timestep |
gens |
Number of generations to simulate |
keep |
In function |
meta |
In function In function |
Details
Functions select.immigrate()
and select.mutate()
are not
really intended for the end user; they use computationally efficient
(and opaque) integer arithmetic.
Author(s)
Robin K. S. Hankin
References
S. P. Hubbell 2001. “The Unified Neutral Theory of Biodiversity”. Princeton University Press.
Examples
data(butterflies)
untb(start=butterflies, prob=0, gens=100)
a <- untb(start=1:10,prob=0.005, gens=1000,keep=TRUE)
plot(species.count(a),type="b")
matplot(species.table(a),type="l",lty=1)
Various functions from Vallade and Houchmandzadeh
Description
Various functions from Vallade and Houchmandzadeh (2003), dealing with analytical solutions of a neutral model of biodiversity
Usage
vallade.eqn5(JM, theta, k)
vallade.eqn7(JM, theta)
vallade.eqn12(J, omega, m, n)
vallade.eqn14(J, theta, m, n)
vallade.eqn16(J, theta, mu)
vallade.eqn17(mu, theta, omega, give=FALSE)
Arguments
J , JM |
Size of the community and metacommunity respectively |
theta |
Biodiversity number
|
k , n |
Abundance |
omega |
Relative abundance |
m |
Immigration probability |
mu |
Scaled immigration probability
|
give |
In function |
Details
Notation follows Vallade and Houchmandzadeh (2003) exactly.
Note
Function vallade.eqn16()
requires the polynom
library,
which is not loaded by default. It will not run for J>50
due to
some stack overflow error.
Function vallade.eqn5()
is identical to function
alonso.eqn6()
Author(s)
Robin K. S. Hankin
References
M. Vallade and B. Houchmandzadeh 2003. “Analytical Solution of a Neutral Model of Biodiversity”, Physical Review E, volume 68. doi: 10.1103/PhysRevE.68.061902
Examples
# A nice check:
JM <- 100
k <- 1:JM
sum(k*vallade.eqn5(JM,theta=5,k)) # should be JM=100 exactly.
# Now, a replication of Figure 3:
omega <- seq(from=0.01, to=0.99,len=100)
f <- function(omega,mu){
vallade.eqn17(mu,theta=5, omega=omega)
}
plot(omega,
omega*5,type="n",xlim=c(0,1),ylim=c(0,5),
xlab=expression(omega),
ylab=expression(omega*g[C](omega)),
main="Figure 3 of Vallade and Houchmandzadeh")
points(omega,omega*sapply(omega,f,mu=0.5),type="l")
points(omega,omega*sapply(omega,f,mu=1),type="l")
points(omega,omega*sapply(omega,f,mu=2),type="l")
points(omega,omega*sapply(omega,f,mu=4),type="l")
points(omega,omega*sapply(omega,f,mu=8),type="l")
points(omega,omega*sapply(omega,f,mu=16),type="l")
points(omega,omega*sapply(omega,f,mu=Inf),type="l")
# Now a discrete version of Figure 3 using equation 14:
J <- 100
omega <- (1:J)/J
f <- function(n,mu){
m <- mu/(J-1+mu)
vallade.eqn14(J=J, theta=5, m=m, n=n)
}
plot(omega,omega*0.03,type="n",main="Discrete version of Figure 3 using
eqn 14")
points(omega,omega*sapply(1:J,f,mu=16))
points(omega,omega*sapply(1:J,f,mu=8))
points(omega,omega*sapply(1:J,f,mu=4))
points(omega,omega*sapply(1:J,f,mu=2))
points(omega,omega*sapply(1:J,f,mu=1))
points(omega,omega*sapply(1:J,f,mu=0.5))
Expected frequency of species
Description
Given a community size, biodiversity parameter \theta
,
and an immigration rate m
, returns the expected frequency of
species with n
individuals, for 0<n\leq J
.
Usage
volkov(J, params, bins = FALSE, give = FALSE)
Arguments
J |
Size of community |
params |
A two-element vector with first element interpreted as
theta, the Fundamental biodiversity parameter and the second, m,
interpreted as the probability of immigration. This argument will
accept the output of |
bins |
Boolean, with default |
give |
Boolean, with |
Value
Returns an object of class “phi”.
Note
The method used is slightly inefficient: the terms to the left of the
integral sign [in Volkov's equation 7] are integrated and this is,
strictly, unnecessary as it is not a function of y
. However,
taking advantage of this fact results in messy code.
Author(s)
Robin K. S. Hankin
References
I. Volkov and others 2003. “Neutral theory and relative species abundance in ecology”. Nature, volume 424, number 28.
See Also
Examples
## Not run:
volkov(J=21457,c(theta=47.226, m=0.1)) # Example in figure 1
## End(Not run)
volkov(J=20,params=c(theta=1,m=0.4))
data(butterflies)
r <- plot(preston(butterflies,n=9,orig=TRUE))
## Not run: jj <- optimal.params(butterflies) # needs PARI/GP
jj <- c(9.99980936124759, 0.991791987473506)
points(r,volkov(no.of.ind(butterflies), jj, bins=TRUE),type="b")
Zero sum multinomial distribution as derived by McKane
Description
The Zero sum multinomial distribution of species abundances as derived by McKane 2004.
Usage
zsm(J, P, m)
Arguments
J |
Size of local community |
P |
Abundance in metacommunity |
m |
Probability of immigration |
Value
Returns a vector of size J
showing the probability of the
stationary abundance being 1,\ldots,J
.
Note
The function uses lgamma()
to avoid numerical overflow
Author(s)
Robin K. S. Hankin
References
A. J. McKane and others 2004. “Analytic solution of Hubbell's model of local community dynamics”. Theoretical Population Biology 65:67-73
Examples
sum(zsm(164,0.1,0.5)) # should be 1
# McKane et al 2004: figure 1.
layout(matrix(1:4,2,2))
par(mai=0.2+rep(0,4))
plot(1,type="n",log="y",ylim=c(1e-9,1),xlim=c(0,64),xlab="",ylab="Ps(N)",
axes=FALSE,main=expression(J==64))
axis(1,pos=1e-9)
axis(2,pos=0,at=10^(-(0:9)))
segments(64,1e-9,64,1)
segments(60,1e-9,64,1e-9)
f <- function(P){points(0:64,zsm(64,P=P,m=0.05),type="l")}
for(i in 1:9){f(i/10)}
f(0.99)
f(0.999)
f(0.01)
f(0.001)
text(07,3.2e-7,adj=0,expression(P==0.999))
text(49,3.2e-7,adj=0,expression(P==0.001))
text(45,0.1,expression(m==0.05))
plot(1,type="n",log="y",ylim=c(1e-5,1),xlim=c(0,64),xlab="",ylab="Ps(N)",
axes=FALSE,main="")
axis(1,pos=1e-5)
axis(2,pos=0,at=10^-(0:5))
segments(60,1e-5,64,1e-5)
segments(64,1e-5,64,1)
par(xpd=FALSE)
g <- function(m){points(0:64,pmax(zsm(64,P=0.1,m=m),1e-5),type="l")}
g(0.0001)
g(0.0005)
g(0.002)
g(0.01)
g(0.02)
g(0.05)
g(0.5)
g(0.999)
text(50,0.4,expression(P==0.1))
plot(1,type="n",log="y",ylim=c(1e-9,1),xlim=c(0,1e5),xlab="",ylab="Ps(N)",
axes=FALSE,main=expression(J==10000))
axis(1,pos=1e-9)
axis(2,pos=0)
segments(1e5,1e-9,1e5,0.1)
h <- function(P){points(0:1e5,pmax(zsm(1e5,P=P,m=0.05),1e-9),type="l")}
for(i in 1:9){h(i/10)}
h(0.01)
h(0.99)
text(75000,0.1,expression(m==0.5))
plot(1,type="n",log="y",ylim=c(1e-40,1),xlim=c(0,1e5),xlab="",ylab="Ps(N)",
axes=FALSE,main="")
axis(1,pos=1e-40)
axis(2,pos=0,at=1/10^c(40,32,24,16,8,0))
segments(1e5,1e-40,1e5,1)
i <- function(m){points(0:1e5,pmax(zsm(1e5,P=0.1,m=m),1e-40),type="l")}
i(0.0001)
i(0.0002)
i(0.0005)
i(0.001)
i(0.002)
i(0.005)
i(0.01)
i(0.02)
i(0.5)
text(60000,1e-4,expression(P==0.1))