Performs Phylogenetic linear regression evaluating intraspecific variability in response and/or predictor variables.
intra_phylm(
formula,
data,
phy,
Vy = NULL,
Vx = NULL,
y.transf = NULL,
x.transf = NULL,
n.intra = 30,
distrib = "normal",
model = "lambda",
track = TRUE,
...
)
The model formula: response~predictor
.
Data frame containing species traits and species names as row names.
A phylogeny (class 'phylo', see ?ape
).
Name of the column containing the standard deviation or the standard error of the response
variable. When information is not available for one taxon, the value can be 0 or NA
.
Name of the column containing the standard deviation or the standard error of the predictor
variable. When information is not available for one taxon, the value can be 0 or NA
Transformation for the response variable (e.g. log
or sqrt
). Please use this
argument instead of transforming data in the formula directly (see also details below).
Transformation for the predictor variable (e.g. log
or sqrt
). Please use this
argument instead of transforming data in the formula directly (see also details below).
Number of times to repeat the analysis generating a random value for response and/or predictor variables.
If NULL, n.intra
= 30
A character string indicating which distribution to use to generate a random value for the response
and/or predictor variables. Default is normal distribution: "normal" (function rnorm
).
Uniform distribution: "uniform" (runif
)
Warning: we recommend to use normal distribution with Vx or Vy = standard deviation of the mean.
The phylogenetic model to use (see Details). Default is lambda
.
Print a report tracking function progress (default = TRUE)
Further arguments to be passed to phylolm
The function intra_phylm
returns a list with the following
components:
formula
: The formula
data
: Original full dataset
sensi.estimates
: Coefficients, aic and the optimised
value of the phylogenetic parameter (e.g. lambda
) for each regression.
N.obs
: Size of the dataset after matching it with tree tips and removing NA's.
stats
: Main statistics for model parameters.CI_low
and CI_high
are the lower
and upper limits of the 95
all.stats
: Complete statistics for model parameters. sd_intra
is the standard deviation
due to intraspecific variation. CI_low
and CI_high
are the lower and upper limits
of the 95
sp.pb
: Species that caused problems with data transformation (see details above).
When Vy or Vx exceed Y or X, respectively, negative (or null) values can be generated, this might cause problems
for data transformation (e.g. log-transformation). In these cases, the function will skip the simulation. This problem can
be solved by increasing n.intra
, changing the transformation type and/or checking the target species in output$sp.pb.
This function fits a phylogenetic linear regression model using phylolm
.
The regression is repeated n.intra
times. At each iteration the function generates a random value
for each row in the dataset using the standard deviation or errors supplied and assuming a normal or uniform distribution.
To calculate means and se for your raw data, you can use the summarySE
function from the
package Rmisc
.
#' All phylogenetic models from phylolm
can be used, i.e. BM
,
OUfixedRoot
, OUrandomRoot
, lambda
, kappa
,
delta
, EB
and trend
. See ?phylolm
for details.
Currently, this function can only implement simple linear models (i.e. \(trait~ predictor\)). In the future we will implement more complex models.
Output can be visualised using sensi_plot
.
Paterno, G. B., Penone, C. Werner, G. D. A. sensiPhy: An r-package for sensitivity analysis in phylogenetic comparative methods. Methods in Ecology and Evolution 2018, 9(6):1461-1467
Martinez, P. a., Zurano, J.P., Amado, T.F., Penone, C., Betancur-R, R., Bidau, C.J. & Jacobina, U.P. (2015). Chromosomal diversity in tropical reef fishes is related to body size and depth range. Molecular Phylogenetics and Evolution, 93, 1-4
Ho, L. S. T. and Ane, C. 2014. "A linear-time algorithm for Gaussian and non-Gaussian trait evolution models". Systematic Biology 63(3):397-408.
# NOT RUN {
# Load data:
data(alien)
# run PGLS accounting for intraspecific variation:
intra <- intra_phylm(gestaLen ~ adultMass, y.transf = log, x.transf = log,
phy = alien$phy[[1]], data = alien$data, Vy = "SD_gesta", n.intra = 30)
# To check summary results:
summary(intra)
# Visual diagnostics
sensi_plot(intra)
# }
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