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Expand Samples or Expand resemblances
The Exe environment matrix does not seem (from Plots>Draftsman Plot or Histogram Plot) to contain notable outliers and can safely be used without transformation of individual variables. It does however need Pre-treatment>Normalise Variables – rename it Abiotic...
Model matrix for 2D Euclidean; Cyclicity (Sea-loch macrofauna)
The other two Model Matrix options are (Type•Cyclicity (factor as cycles)) and (Type•Euclidean 2D). The latter simply calculates, for example, distance between samples in a geographic layout when the x, y co-ordinates of the sample points are not held in a sep...
2-way RELATE for cyclicity
A 2-way RELATE version of the above test where there are no replicates, and the cyclic factor under test is actually nested within a ‘nuisance’ factor whose effect we want to remove, is given by reverting to the full data sheet for the Loch Etive macrofauna sa...
(Leschenault estuarine fish, W Australia)
Veale L et al 2014 J Fish Biol 85: 1320-1354 describe trawl sampling for nearshore estuarine fish in the Leschenault estuary of Western Australia, over 4 regions (B - Basal, L - Lower, U - Upper, A - Apex of the estuary) and 4 seasons (Sp - Spring, S - Summer,...
Rationale for 2nd stage MDS
As seen above, the $\rho$ statistic, which rank correlates the elements of two similarity matrices, can provide a very useful and succinct summary of the extent of agreement between two ordinations (or, to be more precise, of agreement in the high-dimensional ...
Aggregation & transforms (Morlaix macrofauna)
Chapter 10 of CiMC gives several examples of aggregating species matrices to higher taxa – using the Tools>Aggregate routine – and the effect this has on the resulting multivariate (and univariate) analyses. We shall illustrate this with the benthic macrofauna...
Second-stage nMDS (Morlaix macrofauna)
The illustration below has calculated all combinations of species (sp), genus (gn) and family (fm) level data, under no transform (no), square-root (sqr), fourth-root (4th), log(x+1) (log) transforms and reduction to presence/absence (pa), with similarity shee...
2STAGE for resemblance coefficients (Clyde study)
The technique of 2nd stage plots has also been used (Clarke KR, Somerfield PJ, Chapman MG 2006, J Exp Mar Biol Ecol 330: 55-80) to examine the effects of different resemblance coefficient choices on a samples analysis, scaling this in relation to the effects o...
Conclusions on comparing resemblance coefficients
Clarke KR, Somerfield PJ, Chapman MG 2006, J Exp Mar Biol Ecol 330: 55-80 discuss this analysis (and that for several other data sets) in more detail, but to pick out just four general points: a) These 2nd stage plots have common features, irrespective of the ...
2STAGE for displaying ‘interactions’
A very different way of using 2nd stage matrices is best accessed through the alternative entry option in the dialog box for 2STAGE, namely to specify a single similarity matrix with factors defining a 2-way crossed layout of samples (e.g. of sites and times),...
(Phuket coral transect)
Open the workspace Phuket ws, of coral cover for the Ko Phuket transect A, in C:\Examples v7\ Phuket corals, or if not available, open the data files Phuket coral cover 83-87, 88-97 and 98-00, and Tools>Merge them (as in Section 11), taking the defaults to p...
2STAGE for time series and repeated measures
In the context of a 2-factor design, PRIMER makes a 2nd stage matrix very simple to produce but it is less easy to understand what it represents! The structure requires that the factors divide the data into a 2-way layout with no replicates in each cell; the i...
(Tees Bay macrofauna)
The workspace Tees ws was saved in Section 9; if not available open the data Tees macrobenthic abundance from C:\Examples v7\Tees macrobenthos and recalculate Bray-Curtis similarity on the 4th-root transformed abundances for all 192 samples (B-C all), with str...
(Calafuria macroalgae experiment)
The Calafuria macroalgal recolonisation experiment monitored the same physical rock patches over one year, having first cleared the (subtidal) rockface. Replicate patches were tracked for 8 different ‘treatments’, namely different times of year for the clearan...
Other BEST applications
Another situation employing rank correlation ($\rho$) between two resemblance matrices is the BEST (Bio-Env) routine of Section 13, where the biological similarity matrix (‘response’) describes the among-sample relationships of the full community and the secon...
BVStep stepwise selection
There is one fundamental problem with applying BEST (Bio-Env) in many of the above scenarios: the number of variable combinations from the active matrix that must be considered in a full search increases exponentially with the number of variables. For p variab...
Species sets ‘explaining’ the overall pattern
The main application area for the BVStep routine introduced by Clarke KR & Warwick RM 1998, Oecologia 113: 278-289, is what might be termed Bio-Bio, namely searching for subsets of species whose resemblance matrix best matches that of another (fixed) set of sp...
BVStep (Morlaix macrofauna)
Re-open the Morlaix ws workspace in C:\Examples v7\Morlaix macrofauna from earlier in this section, or since this is all that is needed, just open the data file Morlaix macrofauna abundance into a clear workspace. It consists of 21 sampling times and 251specie...
BVStep starting and stopping options
On B-C on 4rt, Analyse>BEST>(Method•BVSTEP) & (Worksheet: 4rt data), taking the defaults for all other entries (Spearman correlations, the suggested Bray-Curtis similarity, all 100 species Available for selection, and the permutation test ignored – a test of $...
BVStep from random starts
Starting the iterative search process from a blank species list is certainly not guaranteed to get you to the best solution (minimum number of species which give $\rho \ge$0.95) – it is easy to get trapped in a local optimum which in not the globally best solu...