Table 1.
case-study, signal variable | model, rank | constrained tree |
unconstrained tree |
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
AICc | AICw | r | t1/2 (support region) | vy (support region) | AICc | AICw | r | t1/2 (support region) | vy (support region) | ||
frogs, n = 32 species | |||||||||||
call amplitude modulation | 1. phylogeny: null | 292.1 | 0.37 | n.a. | 0 (0–10) | 440 (260–760) | 290.5 | 0.37 | n.a. | 20 (0–140) | 440 (300–∞) |
2. ecology: sympatry | 294.4 | 0.12 | ∼0.16a | 1 (0–10) | 420 (260–720) | 292.9 | 0.11 | ||||
3. ecology: microhabitatb | 294.2 | 0.13 | 292.5 | 0.14 | −0.14 | 20 (0–160) | 430 (280–∞) | ||||
4. ecology: noisec | 294.2 | 0.13 | 292.8 | 0.12 | |||||||
5. social: SSD | 294.5 | 0.11 | 293.1 | 0.10 | |||||||
6. allometry: body size | 294.7 | 0.10 | 292.6 | 0.13 | |||||||
7. ecology: macrohabitat | 296.7 | 0.04 | 294.8 | 0.04 | |||||||
call duration | 1. ecology: microhabitatb | −11.82 | 0.81 | 0.45 | 900 (170–∞) | 30 (0–70) | 57.1 | 0.12 | |||
2. phylogeny: null | −7.20 | 0.08 | 54.6 | 0.42 | n.a. | 460 (870–∞) | 10 (0–20) | ||||
3. ecology: sympatry | −5.16 | 0.03 | 57.3 | 0.11 | |||||||
4. allometry: body size | −5.20 | 0.03 | 57.2 | 0.11 | |||||||
5. ecology: noisec | −4.63 | 0.02 | 57.3 | 0.11 | |||||||
6. social: SSD | −4.59 | 0.02 | 57.3 | 0.11 | |||||||
7. ecology: macrohabitat | −3.53 | 0.01 | 60.0 | 0.03 | |||||||
birds (distantly related), n = 23 species | |||||||||||
syllable repertoire size | 1. allometry: body size | 46.2 | 0.35 | 0.35 | 75 (25–∞) | 25 (0–700) | 47.4 | 0.34 | 0.34 | 500 (25–∞) | 175 (0–700) |
2. phylogeny: null | 46.3 | 0.33 | n.a. | 300 (25–∞) | 125 (0–825) | 47.4 | 0.34 | n.a. | 175 (25–∞) | 75 (0–825) | |
3. ecology: breeding range | 48.6 | 0.11 | 49.7 | 0.11 | |||||||
4. ecology: macrohabitat | 48.7 | 0.10 | 50.0 | 0.09 | |||||||
5. social: extra-pair paternity | 48.9 | 0.09 | 49.9 | 0.10 | |||||||
6. social: mating system | 52.1 | 0.02 | 53.0 | 0.02 | |||||||
song repertoire size | 1. phylogeny: null | 55.0 | 0.46 | n.a. | 975 (0–∞) | 600 (0–∞) | 56.3 | 0.46 | n.a. | 975 (0–∞) | 575 (0–∞) |
2. ecology: breeding range | 57.0 | 0.17 | 0.21 | 950 (0–∞) | 550 (0–∞) | 58.3 | 0.17 | 0.20 | 975 (0–∞) | 575 (0–∞) | |
3. allometry: body size | 57.9 | 0.11 | 59.2 | 0.11 | |||||||
4. social: extra-pair paternity | 58.0 | 0.10 | 59.2 | 0.11 | |||||||
5. ecology: macrohabitat | 58.0 | 0.10 | 59.1 | 0.11 | |||||||
6. social: mating system | 59.2 | 0.06 | 61.3 | 0.04 | |||||||
birds (closely related), n = 23 species | |||||||||||
syllable repertoire | 1. ecology: migration | −41.4 | 0.42 | ∼0.52d | ∞ (630–∞) | 10 (0–20) | −37.5 | 0.13 | |||
2. phylogeny: null | −41.1 | 0.36 | n.a. | 940 (500–∞) | 10 (0–30) | −40.5 | 0.57 | n.a. | 910 (480–∞) | 10 (0–30) | |
3. ecology: macrohabitat | −38.7 | 0.11 | −37.8 | 0.15 | |||||||
4. allometry: body size | −38.7 | 0.11 | −38.0 | 0.16 | |||||||
syllable duration | 1. phylogeny: null | −64.1 | 0.66 | n.a. | ∞ (830–∞) | 10 (0–20) | −64.2 | 0.66 | n.a. | ∞ (830–∞) | 10 (0–20) |
2. ecology: macrohabitat | −61.2 | 0.15 | −61.3 | 0.16 | |||||||
3. allometry: body size | −61.2 | 0.15 | −61.2 | 0.15 | |||||||
4. ecology: migration | −57.9 | 0.03 | −58.1 | 0.03 | |||||||
song duration | 1. phylogeny: null | −57.8 | 0.64 | n.a. | ∞ (780–∞) | 10 (0–20) | −52.2 | 0.11 | |||
2. allometry: body size | −55.2 | 0.27 | −55.0 | 0.43 | 0.28 | ∞ (780–∞) | 10 (0–20) | ||||
3. ecology: macrohabitat | −54.9 | 0.15 | −54.6 | 0.35 | 0.05 | ∞ (780–∞) | 10 (0–20) | ||||
4. ecology: migration | −52.1 | 0.06 | −52.2 | 0.11 |
aThere are several prominent outliers making direct interpretation of this coefficient misleading (figure 1a).
bMicrohabitat was defined as the height (m) of call sites above ground.
cThe level of background noise potentially experienced by a species was determined by whether species were reported to call near streams.
dThe standard errors of parameter values for migration were very large making biological interpretation difficult.