The function estimates any of the 24 indices of beta diversity reviewed by Koleff et al. (2003). Alternatively, it finds the co-occurrence frequencies for triangular plots (Koleff et al. 2003).
1 2 3 4 5
Community data matrix, or the
The index of beta diversity as defined in Koleff et al.
(2003), Table 1. You can use either the subscript of β or
the number of the index. See argument
Order sites by increasing number of species. This will influence the configuration in the triangular plot and non-symmetric indices.
Show the numbers, subscript names and the defining equations of the indices and exit.
Return scores suitable for triangular plotting of
Other arguments to functions.
The most commonly used index of beta diversity is β_w =
S/α - 1, where S is the total number of species, and
α is the average number of species per site (Whittaker
1960). A drawback of this model is that S increases with
sample size, but the expectation of α remains constant,
and so the beta diversity increases with sample size. A solution to
this problem is to study the beta diversity of pairs of sites. If we
denote the number of species shared between two sites as a and
the numbers of unique species (not shared) as b and c,
then S = a + b + c and α = (2 a + b + c)/2 so that
β_w = (b+c)/(2 a + b + c). This is the Sørensen
dissimilarity as defined in vegan function
vegdist with argument
binary = TRUE. Many
other indices are dissimilarity indices as well.
betadiver finds all indices reviewed by Koleff et
al. (2003). All these indices could be found with function
designdist, but the current function provides a
conventional shortcut. The function only finds the indices. The proper
analysis must be done with functions such as
The indices are directly taken from Table 1 of Koleff et al. (2003),
and they can be selected either by the index number or the subscript
name used by Koleff et al. The numbers, names and defining equations
can be seen using
betadiver(help = TRUE). In all cases where
there are two alternative forms, the one with the term -1 is
used. There are several duplicate indices, and the number of distinct
alternatives is much lower than 24 formally provided. The formulations
used in functions differ occasionally from those in Koleff et
al. (2003), but they are still mathematically equivalent. With
method = NA, no index is calculated, but instead an object of
betadiver is returned. This is a list of elements
plot can be used to
display the proportions of these elements in triangular plot as
suggested by Koleff et al. (2003), and
scores extracts the
triangular coordinates or the raw scores. Function
invisibly the triangular coordinates as an
method = NA, the function returns an object of
"betadisper" with elements
method is specified, the function returns a
"dist" object which can be used in any function analysing
dissimilarities. For beta diversity, particularly useful functions
betadisper to study the betadiversity in groups,
adonis for any model, and
compare beta diversities to other dissimilarities or distances
(including geographical distances). Although
"dist" object, some indices are similarities and
cannot be used as such in place of dissimilarities, but that is a
severe user error. Functions 10 (
"j") and 11 (
are two such similarity indices.
Some indices return similarities instead of dissimilarities.
Baselga, A. (2010) Partitioning the turnover and nestedness components of beta diversity. Global Ecology and Biogeography 19, 134–143.
Koleff, P., Gaston, K.J. and Lennon, J.J. (2003) Measuring beta diversity for presence-absence data. Journal of Animal Ecology 72, 367–382.
Whittaker, R.H. (1960) Vegetation of Siskiyou mountains, Oregon and California. Ecological Monographs 30, 279–338.
designdist for an alternative to implement all
vegdist for some canned alternatives,
mantel for analysing beta diversity objects.
nestedbetajac implement decomposition beta diversity
measures (Sørensen and Jaccard) into turnover and
nestedness components following Baselga (2010).
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Loading required package: permute Loading required package: lattice This is vegan 2.4-3 1 "w" = (b+c)/(2*a+b+c) 2 "-1" = (b+c)/(2*a+b+c) 3 "c" = (b+c)/2 4 "wb" = b+c 5 "r" = 2*b*c/((a+b+c)^2-2*b*c) 6 "I" = log(2*a+b+c) - 2*a*log(2)/(2*a+b+c) - ((a+b)*log(a+b) + (a+c)*log(a+c)) / (2*a+b+c) 7 "e" = exp(log(2*a+b+c) - 2*a*log(2)/(2*a+b+c) - ((a+b)*log(a+b) + (a+c)*log(a+c)) / (2*a+b+c))-1 8 "t" = (b+c)/(2*a+b+c) 9 "me" = (b+c)/(2*a+b+c) 10 "j" = a/(a+b+c) 11 "sor" = 2*a/(2*a+b+c) 12 "m" = (2*a+b+c)*(b+c)/(a+b+c) 13 "-2" = pmin(b,c)/(pmax(b,c)+a) 14 "co" = (a*c+a*b+2*b*c)/(2*(a+b)*(a+c)) 15 "cc" = (b+c)/(a+b+c) 16 "g" = (b+c)/(a+b+c) 17 "-3" = pmin(b,c)/(a+b+c) 18 "l" = (b+c)/2 19 "19" = 2*(b*c+1)/(a+b+c)/(a+b+c-1) 20 "hk" = (b+c)/(2*a+b+c) 21 "rlb" = a/(a+c) 22 "sim" = pmin(b,c)/(pmin(b,c)+a) 23 "gl" = 2*abs(b-c)/(2*a+b+c) 24 "z" = (log(2)-log(2*a+b+c)+log(a+b+c))/log(2)  0 0
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