Table 1 Model outputs of linear mixed models for the key explanatory variables of the ‘baseline innate immune models’ (response variables: hemagglutination, hemolysis, bacteria-killing capacity and baseline haptoglobin) and ‘innate immune response model’ (response variable: haptoglobin response, quantified as the difference between baseline haptoglobin concentration and haptoglobin concentration post-injection of lipopolysaccharides).

From: Parental morph combination does not influence innate immune function in nestlings of a colour-polymorphic African raptor

Measurement

Study period

N

Model output ‘pair morph’ explanatory variable

Model output ‘body mass index’ explanatory variable

Like

Mixed

Estimate

SE

χ2

ndf

ddf

P

Estimate

SE

χ2

ndf

ddf

P

Baseline innate immune models

Hemagglutination

2015–2019

98

81

0.247

0.172

2.07

1

172

0.156

0.003

0.002

3.94

1

172

0.047

Hemolysis

2015–2019

98

81

0.030

0.147

0.04

1

172

0.837

0.002

0.001

1.34

1

172

0.225

Baseline haptoglobin

2015–2019

99

78

0.012

0.021

0.32

1

169

0.574

-0.001

0.001

0.24

1

169

0.624

Bacteria killing

2015–2019

91

77

0.008

0.030

0.08

1

161

0.783

0.001

0.001

0.90

1

161

0.344

Innate immune response model

  

Haptoglobin response

2018–2019

30

19

-0.158

0.307

0.27

1

41

0.607

-0.001

0.003

0.16

1

41

0.694

  1. Key explanatory variables are parental ‘pair morph’ (factor in two levels: ‘like-morph’: dark-dark D♂D♀ and light-light L♂L♀; or ‘mixed-morph’: dark–light D♂L♀ and light–dark L♂D♀, the reference category is ‘mixed-morph') or the ‘body mass index’. All ‘baseline innate immune models’ were fitted with individual ‘sex’ (male or female), ‘age’ (numeric, in days: 20–35), ‘brood size’ (numeric, 1–3), ‘seasonality’ (numeric, week number: 22–46), and ‘time of the day’ when sample was obtained (numeric, hour: 7–17) as additional co-variates and territory ID as a random factor. Bacteria-killing and baseline haptoglobin concentration were log-transformed, the baseline haptoglobin model included an additional co-variate: a reading at 450 nm to control for plasma redness. The ‘innate immune response model’ was fitted with two baseline readings (650 nm and 450 nm) to control for initial haptoglobin concentration and plasma redness, ‘sex’, ‘age’ (numeric, week number: 22–35), ‘brood size’, ‘seasonality’ (numeric, week number: 23–43), as co-variates and territory ID as a random factor. All response variables were scaled and centred to the mean of the year, whereas all continuous variables were scaled. Study period (in years), sample size (N, for mixed- and like-morph), numerator and denominatior degrees of freedom (ndf and ddf) given in respective columns. See tables S1-S9 for full model outputs.