# Function for Fitting Latent Factor Multi-species N-mixture Models

`lfMsNMix.Rd`

Function for fitting multi-species N-mixture models with species correlations (i.e., an abundance-based joint species distribution model with imperfect detection). We use a factor modeling approach for dimension reduction.

## Usage

```
lfMsNMix(abund.formula, det.formula, data, inits, priors,
tuning, n.factors, n.batch, batch.length, accept.rate = 0.43,
family = 'Poisson', n.omp.threads = 1, verbose = TRUE, n.report = 100,
n.burn = round(.10 * n.samples), n.thin = 1,
n.chains = 1, ...)
```

## Arguments

- abund.formula
a symbolic description of the model to be fit for the abundance portion of the model using R's model syntax. Only right-hand side of formula is specified. See example below. Random intercepts and slopes are allowed using lme4 syntax (Bates et al. 2015).

- det.formula
a symbolic description of the model to be fit for the detection portion of the model using R's model syntax. Only right-hand side of formula is specified. See example below. Random intercepts and slopes are allowed using lme4 syntax (Bates et al. 2015).

- data
a list containing data necessary for model fitting. Valid tags are

`y`

,`abund.covs`

,`det.covs`

,`coords`

, and`offset`

.`y`

is a three-dimensional array of observed count data with first dimension equal to the number of species, second dimension equal to the number of sites, and third dimension equal to the maximum number of replicates at a given site.`abund.covs`

is a matrix or data frame containing the variables used in the abundance portion of the model, with \(J\) rows for each column (variable).`det.covs`

is a list of variables included in the detection portion of the model. Each list element is a different detection covariate, which can be site-level or observational-level. Site-level covariates are specified as a vector of length \(J\) while observation-level covariates are specified as a matrix or data frame with the number of rows equal to \(J\) and number of columns equal to the maximum number of replicates at a given site.`coords`

is a matrix or data frame with two columns that contain the spatial coordinates of each site. Note that`spAbundance`

assumes coordinates are specified in a projected coordinate system.`offset`

is an offset to use in the abundance model (e.g., an area offset). This can be either a single value or a vector with an offset for each site (e.g., if survey area differed in size).- inits
a list with each tag corresponding to a parameter name. Valid tags are

`alpha.comm`

,`beta.comm`

,`beta`

,`alpha`

,`tau.sq.beta`

,`tau.sq.alpha`

,`sigma.sq.mu`

,`sigma.sq.p`

,`lambda`

,`w`

,`kappa`

, and`N`

.`sigma.sq.mu`

and`sigma.sq.p`

are only relevant when including random effects in the abundance and detection portion of the model, respectively.`kappa`

is only relevant when`family = 'NB'`

. The value portion of each tag is the parameter's initial value. See`priors`

description for definition of each parameter name. Additionally, the tag`fix`

can be set to`TRUE`

to fix the starting values across all chains. If`fix`

is not specified (the default), starting values are varied randomly across chains.- priors
a list with each tag corresponding to a parameter name. Valid tags are

`beta.comm.normal`

,`alpha.comm.normal`

,`tau.sq.beta.ig`

,`tau.sq.alpha.ig`

,`sigma.sq.mu.ig`

,`sigma.sq.p.ig`

, and`kappa.unif`

. Community-level abundance (`beta.comm`

) and detection (`alpha.comm`

) regression coefficients are assumed to follow a normal distribution. The hyperparameters of the normal distribution are passed as a list of length two with the first and second elements corresponding to the mean and variance of the normal distribution, which are each specified as vectors of length equal to the number of coefficients to be estimated or of length one if priors are the same for all coefficients. If not specified, prior means are set to 0 and prior variances for the abundance coefficients are set to 100 and for the detection coefficients are set to 2.72. Community-level variance parameters for abundance (`tau.sq.beta`

) and detection (`tau.sq.alpha`

) are assumed to follow an inverse Gamma distribution. The hyperparameters of the inverse gamma distribution are passed as a list of length two with the first and second elements corresponding to the shape and scale parameters, which are each specified as vectors of length equal to the number of coefficients to be estimated or a single value if all parameters are assigned the same prior. If not specified, prior shape and scale parameters are set to 0.1.`sigma.sq.mu`

and`sigma.sq.p`

are the random effect variances for any abundance or detection random effects, respectively, and are assumed to follow an inverse Gamma distribution. The hyperparameters of the inverse-Gamma distribution are passed as a list of length two with first and second elements corresponding to the shape and scale parameters, respectively, which are each specified as vectors of length equal to the number of random effects or of length one if priors are the same for all random effect variances.`kappa`

is the negative binomial dispersion parameter for each species and is assumed to follow a uniform distribution. The hyperparameters of the uniform distribution are passed as a list of length two with first and second elements corresponding to the lower and upper bounds of the uniform distribution, respectively, which are each specified as vectors of length equal to the number of species or of length one if priors are the same for all species-specific dispersion parameters.- tuning
a list with each tag corresponding to a parameter name, whose value defines the initial variance of the adaptive sampler. Valid tags are

`beta`

,`alpha`

,`beta.star`

(the abundance random effect values),`alpha.star`

(the detection random effect values),`lambda`

(the latent factor loadings),`w`

(the latent factors), and`kappa`

. See Roberts and Rosenthal (2009) for details.- n.factors
the number of factors to use in the latent factor model approach. Typically, the number of factors is set to be small (e.g., 4-5) relative to the total number of species in the community, which will lead to substantial decreases in computation time. However, the value can be anywhere between 1 and N (the number of species in the community).

- n.batch
the number of MCMC batches in each chain to run for the Adaptive MCMC sampler. See Roberts and Rosenthal (2009) for details.

- batch.length
the length of each MCMC batch in each chain to run for the Adaptive MCMC sampler. See Roberts and Rosenthal (2009) for details.

- accept.rate
target acceptance rate for Adaptive MCMC. Default is 0.43. See Roberts and Rosenthal (2009) for details.

- family
the distribution to use for the latent abundance process. Currently supports

`'NB'`

(negative binomial) and`'Poisson'`

.- n.omp.threads
a positive integer indicating the number of threads to use for SMP parallel processing. The package must be compiled for OpenMP support. For most Intel-based machines, we recommend setting

`n.omp.threads`

up to the number of hypterthreaded cores. Note,`n.omp.threads`

> 1 might not work on some systems. Currently only relevant for spatial models.- verbose
if

`TRUE`

, messages about data preparation, model specification, and progress of the sampler are printed to the screen. Otherwise, no messages are printed.- n.report
the interval to report MCMC progress.

- n.burn
the number of samples out of the total

`n.samples`

to discard as burn-in for each chain. By default, the first 10% of samples is discarded.- n.thin
the thinning interval for collection of MCMC samples. The thinning occurs after the

`n.burn`

samples are discarded. Default value is set to 1.- n.chains
the number of chains to run in sequence.

- ...
currently no additional arguments

## References

Bates, Douglas, Martin Maechler, Ben Bolker, Steve Walker (2015). Fitting Linear Mixed-Effects Models Using lme4. Journal of Statistical Software, 67(1), 1-48. doi:10.18637/jss.v067.i01 .

Royle, J. A. (2004). N‐mixture models for estimating population size from spatially replicated counts. Biometrics, 60(1), 108-115.

Yamaura, Y., Royle, J. A., Shimada, N., Asanuma, S., Sato, T., Taki, H., & Makino, S. I. (2012). Biodiversity of man-made open habitats in an underused country: a class of multispecies abundance models for count data. Biodiversity and Conservation, 21(6), 1365-1380.

## Author

Jeffrey W. Doser doserjef@msu.edu,

## Value

An object of class `lfMsNMix`

that is a list comprised of:

- beta.comm.samples
a

`coda`

object of posterior samples for the community level abundance regression coefficients.- alpha.comm.samples
a

`coda`

object of posterior samples for the community level detection regression coefficients.- tau.sq.beta.samples
a

`coda`

object of posterior samples for the abundance community variance parameters.- tau.sq.alpha.samples
a

`coda`

object of posterior samples for the detection community variance parameters.- beta.samples
a

`coda`

object of posterior samples for the species level abundance regression coefficients.- alpha.samples
a

`coda`

object of posterior samples for the species level detection regression coefficients.- lambda.samples
a

`coda`

object of posterior samples for the latent factor loadings.- w.samples
a three-dimensional array of posterior samples for the latent effects for each latent factor.

- kappa.samples
a

`coda`

object of posterior samples for the species level abundance dispersion parameters. Only included when`family = 'NB'`

.- N.samples
a three-dimensional array of posterior samples for the latent abundance values for each species.

- mu.samples
a three-dimensional array of posterior samples for the latent expected abundance values for each species.

- sigma.sq.mu.samples
a

`coda`

object of posterior samples for variances of random effects included in the abundance portion of the model. Only included if random effects are specified in`abund.formula`

.- sigma.sq.p.samples
a

`coda`

object of posterior samples for variances of random effects included in the detection portion of the model. Only included if random effects are specified in`det.formula`

.- beta.star.samples
a

`coda`

object of posterior samples for the abundance random effects. Only included if random effects are specified in`abund.formula`

.- alpha.star.samples
a

`coda`

object of posterior samples for the detection random effects. Only included if random effects are specified in`det.formula`

.- rhat
a list of Gelman-Rubin diagnostic values for some of the model parameters.

- ESS
a list of effective sample sizes for some of the model parameters.

- run.time
MCMC sampler execution time reported using

`proc.time()`

.

The return object will include additional objects used for
subsequent prediction and/or model fit evaluation. Note that detection probability
estimated values are not included in the model object, but can be extracted
using `fitted()`

.

## Examples

```
set.seed(408)
J.x <- 8
J.y <- 8
J <- J.x * J.y
n.rep <- sample(5, size = J, replace = TRUE)
n.sp <- 6
# Community-level covariate effects
# Abundance
beta.mean <- c(0, 0.5)
p.abund <- length(beta.mean)
tau.sq.beta <- c(0.2, 1.2)
# Detection
alpha.mean <- c(0, 0.5, 0.8)
tau.sq.alpha <- c(0.2, 1, 1.5)
p.det <- length(alpha.mean)
# Random effects
mu.RE <- list()
p.RE <- list()
# Draw species-level effects from community means.
beta <- matrix(NA, nrow = n.sp, ncol = p.abund)
alpha <- matrix(NA, nrow = n.sp, ncol = p.det)
for (i in 1:p.abund) {
beta[, i] <- rnorm(n.sp, beta.mean[i], sqrt(tau.sq.beta[i]))
}
for (i in 1:p.det) {
alpha[, i] <- rnorm(n.sp, alpha.mean[i], sqrt(tau.sq.alpha[i]))
}
n.factors <- 3
dat <- simMsNMix(J.x = J.x, J.y = J.y, n.rep = n.rep, n.sp = n.sp, beta = beta, alpha = alpha,
mu.RE = mu.RE, p.RE = p.RE, sp = FALSE, family = 'Poisson',
factor.model = TRUE, n.factors = n.factors)
y <- dat$y
X <- dat$X
X.p <- dat$X.p
X.re <- dat$X.re
X.p.re <- dat$X.p.re
coords <- dat$coords
# Package all data into a list
abund.covs <- X
colnames(abund.covs) <- c('int', 'abund.cov.1')
det.covs <- list(det.cov.1 = as.data.frame(X.p[, , 2]),
det.cov.2 = as.data.frame(X.p[, , 3]))
data.list <- list(y = y,
abund.covs = abund.covs,
det.covs = det.covs,
coords = coords)
prior.list <- list(beta.comm.normal = list(mean = rep(0, p.abund),
var = rep(100, p.abund)),
alpha.comm.normal = list(mean = rep(0, p.det),
var = rep(2.72, p.det)),
tau.sq.beta.ig = list(a = 0.1, b = 0.1),
tau.sq.alpha.ig = list(a = 0.1, b = 0.1))
inits.list <- list(beta.comm = 0, alpha.comm = 0,
beta = 0, alpha = 0,
tau.sq.beta = 0.5, tau.sq.alpha = 0.5,
N = apply(y, c(1, 2), max, na.rm = TRUE))
tuning.list <- list(beta = 0.5, alpha = 0.5, lambda = 0.5, w = 0.5)
n.batch <- 4
batch.length <- 25
n.burn <- 0
n.thin <- 1
n.chains <- 1
out <- lfMsNMix(abund.formula = ~ abund.cov.1,
det.formula = ~ det.cov.1 + det.cov.2,
data = data.list,
n.batch = n.batch,
inits = inits.list,
priors = prior.list,
tuning = tuning.list,
batch.length = batch.length,
n.omp.threads = 1,
n.factors = n.factors,
verbose = TRUE,
n.report = 1,
n.burn = n.burn,
n.thin = n.thin,
n.chains = n.chains)
#> ----------------------------------------
#> Preparing to run the model
#> ----------------------------------------
#> lambda is not specified in initial values.
#> Setting initial values of the lower triangle to 0
#> w is not specified in initial values.
#> Setting initial value to 0
#> ----------------------------------------
#> Model description
#> ----------------------------------------
#> Latent Factor Multi-species Poisson N-Mixture model fit with 64 sites and 6 species.
#>
#> Samples per Chain: 100
#> Burn-in: 0
#> Thinning Rate: 1
#> Number of Chains: 1
#> Total Posterior Samples: 100
#>
#> Using 3 latent factors.
#>
#> Source compiled with OpenMP support and model fit using 1 thread(s).
#>
#> Adaptive Metropolis with target acceptance rate: 43.0
#> ----------------------------------------
#> Chain 1
#> ----------------------------------------
#> Sampling ...
#> Batch: 1 of 4, 25.00%
#> Species Parameter Acceptance Tuning
#> 1 beta[1] 12.0 0.49010
#> 1 alpha[1] 20.0 0.49010
#> 2 beta[1] 24.0 0.49010
#> 2 alpha[1] 28.0 0.49010
#> 3 beta[1] 4.0 0.49010
#> 3 alpha[1] 4.0 0.49010
#> 4 beta[1] 28.0 0.49010
#> 4 alpha[1] 36.0 0.49010
#> 5 beta[1] 28.0 0.49010
#> 5 alpha[1] 56.0 0.51010
#> 6 beta[1] 24.0 0.49010
#> 6 alpha[1] 28.0 0.49010
#> -------------------------------------------------
#> Batch: 2 of 4, 50.00%
#> Species Parameter Acceptance Tuning
#> 1 beta[1] 12.0 0.48522
#> 1 alpha[1] 28.0 0.48522
#> 2 beta[1] 8.0 0.48522
#> 2 alpha[1] 16.0 0.48522
#> 3 beta[1] 8.0 0.48522
#> 3 alpha[1] 28.0 0.48522
#> 4 beta[1] 12.0 0.48522
#> 4 alpha[1] 32.0 0.48522
#> 5 beta[1] 24.0 0.48522
#> 5 alpha[1] 32.0 0.50503
#> 6 beta[1] 28.0 0.48522
#> 6 alpha[1] 24.0 0.48522
#> -------------------------------------------------
#> Batch: 3 of 4, 75.00%
#> Species Parameter Acceptance Tuning
#> 1 beta[1] 4.0 0.48039
#> 1 alpha[1] 28.0 0.48039
#> 2 beta[1] 16.0 0.48039
#> 2 alpha[1] 24.0 0.48039
#> 3 beta[1] 0.0 0.48039
#> 3 alpha[1] 12.0 0.48039
#> 4 beta[1] 20.0 0.48039
#> 4 alpha[1] 28.0 0.48039
#> 5 beta[1] 24.0 0.48039
#> 5 alpha[1] 44.0 0.51010
#> 6 beta[1] 36.0 0.48039
#> 6 alpha[1] 24.0 0.48039
#> -------------------------------------------------
#> Batch: 4 of 4, 100.00%
summary(out, level = 'community')
#>
#> Call:
#> lfMsNMix(abund.formula = ~abund.cov.1, det.formula = ~det.cov.1 +
#> det.cov.2, data = data.list, inits = inits.list, priors = prior.list,
#> tuning = tuning.list, n.factors = n.factors, n.batch = n.batch,
#> batch.length = batch.length, n.omp.threads = 1, verbose = TRUE,
#> n.report = 1, n.burn = n.burn, n.thin = n.thin, n.chains = n.chains)
#>
#> Samples per Chain: 100
#> Burn-in: 0
#> Thinning Rate: 1
#> Number of Chains: 1
#> Total Posterior Samples: 100
#> Run Time (min): 0.0035
#>
#> ----------------------------------------
#> Community Level
#> ----------------------------------------
#> Abundance Means (log scale):
#> Mean SD 2.5% 50% 97.5% Rhat ESS
#> (Intercept) 0.4613 0.3386 -0.2351 0.4702 1.1671 NA 35
#> abund.cov.1 0.2680 0.2898 -0.3028 0.2676 0.8098 NA 100
#>
#> Abundance Variances (log scale):
#> Mean SD 2.5% 50% 97.5% Rhat ESS
#> (Intercept) 0.7488 0.8101 0.0826 0.5316 2.6159 NA 100
#> abund.cov.1 0.5395 0.4193 0.0977 0.4270 1.6712 NA 53
#>
#> Detection Means (logit scale):
#> Mean SD 2.5% 50% 97.5% Rhat ESS
#> (Intercept) 0.1751 0.1895 -0.3469 0.1963 0.4395 NA 58
#> det.cov.1 0.2027 0.5211 -0.7551 0.1788 1.0672 NA 100
#> det.cov.2 0.4946 0.4365 -0.3495 0.4647 1.4335 NA 100
#>
#> Detection Variances (logit scale):
#> Mean SD 2.5% 50% 97.5% Rhat ESS
#> (Intercept) 0.1987 0.1789 0.0398 0.1545 0.7396 NA 23
#> det.cov.1 1.7934 1.5814 0.1569 1.2905 6.0634 NA 100
#> det.cov.2 1.8620 1.4946 0.3413 1.3768 6.0173 NA 100
```