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#'
#' Each prey fatty acid signature is systematically removed from the
#' supplied prey database and its QFASA diet estimate is obtained by
#' treating the individual as a predator.
#'
#' @export
#'
#' @param preybase first column is name of species and remaining columns are fatty acids.
#' @param dist.meas see help file for \code{\link{p.QFASA}}.
#' @param gamma see help file for \code{\link{p.QFASA}}.
#' @return diet estimate
#'
#' @examples
#' data(preyFAs)
#' my.preybase <- preyFAs[, -c(1,3)]
#'
#' # Note: uncomment examples to run. CRAN tests fail because execution time > 5 seconds
#' # diets.out <- prey.on.prey(my.preybase, 2)
#' # round(MEANmeth(diets.out), 3)
#'
prey.on.prey <-function(preybase,dist.meas,gamma=1)
{
preybase[, -1] <- preybase[,-1]/apply(preybase[, -1], 1, sum)
sort.preytype <- order(preybase[, 1])
preybase <- preybase[sort.preytype,]
groups <- factor(preybase[, 1], unique(preybase[, 1]))
for( j in 1:nrow(preybase))
{
pred.sig <-preybase[j, -1]
prey.matrix <- MEANmeth(preybase[-j, ])
result <- p.QFASA(pred.sig,
prey.matrix,
cal.mat = rep(1,length(pred.sig)),
dist.meas,
gamma,
ext.fa = colnames(prey.matrix))
diet.est <- as.data.frame(result$`Diet Estimates`)
if(j == 1) {
DE.df<-diet.est
}
else {
DE.df <- rbind(DE.df, diet.est)
}
}
DE.df <- cbind(groups, DE.df)
dimnames(DE.df)[[2]] <- c("Species", levels(groups))
return(DE.df)
}
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