Table 1.
Modularity hypothesis | Buzz-bee (n = 16) | Mixed-vertebrate (n = 8) | Passerine (n = 6) | Merianieae | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|
CR | p | Z | CR | p | Z | CR | p | Z | CR | p | |
Hypothesis 1 | 0.815 | 0.001 | 2.353 | 1.100 | 0.653 | 0.286 | 1.077 | 0.318 | 0.287 | 1.527 | 1.000 |
Hypothesis 2 | 0.858 | 0.026 | 2.069 | 1.011 | 0.319 | 0.506 | 1.025 | 0.192 | 0.499 | 0.993 | 0.25 |
Hypothesis 3 | 0.935 | 0.051 | 1.889 | 0.994 | 0.203 | 0.767 | 1.012 | 0.101 | 1.117 | 0.963 | 0.113 |
Hypothesis 4 | 0.787 | 0.001 | 5.727 | 0.947 | 0.036 | 2.196 | 0.831 | 0.001 | 13.172 | 1.020 | 0.345 |
Hypothesis 5 | 0.812 | 0.001 | 3.423 | 0.977 | 0.070 | 1.579 | 0.917 | 0.005 | 4.270 | 0.977 | 0.124 |
Highest degrees of modularity are present in the buzz-bee syndrome and lowest in the mixed-vertebrate syndrome, analyses of evolutionary modularity accounting for phylogenetic relatedness (column Merianieae) show significant modularity in Hypotheses 3, 4 and 5
p – p-value < 0.05 (in italics and bold) indicates significantly smaller CR than expected when no modularity is present
CR covariance ratio, Z effect sizes of CR