Data from: An analysis of mating biases in trees
Data files
Dec 10, 2019 version files 10.56 MB
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Distance_Kinship_Matings__Acer_pictum.csv
172.18 KB
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Distance_Kinship_Matings__Baillonella_toxisperma.csv
126.76 KB
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Distance_Kinship_Matings__Bertholletia_excelsa.csv
345.38 KB
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Distance_Kinship_Matings__Cariniana_legalis.csv
87.53 KB
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Distance_Kinship_Matings__Catstanopsis_sieboldii.csv
391.84 KB
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Distance_Kinship_Matings__Dysoxylum_malabricum.csv
1.09 MB
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Distance_Kinship_Matings__Entandrophragma_cylindricum.csv
1.23 MB
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Distance_Kinship_Matings__Erythrophleum_suaveolens.csv
627.98 KB
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Distance_Kinship_Matings__Fraxinus_excelsior.csv
917.48 KB
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Distance_Kinship_Matings__Glionnetia_sericea.csv
858.78 KB
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Distance_Kinship_Matings__Jacaranda_copaia.csv
1.09 MB
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Distance_Kinship_Matings__Oenocarpus_bataua.csv
746.23 KB
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Distance_Kinship_Matings__Quercus_petreae.csv
507.28 KB
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Distance_Kinship_Matings__Quercus_robur.csv
329.61 KB
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Distance_Kinship_Matings__Shorea_xanthophylla.csv
645.97 KB
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Distance_Kinship_Matings__Vateria_indica.csv
147.07 KB
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Distance_Kinship_Matings_Abies_pinsapo.csv
461.30 KB
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Distance_Kinship_Matings_Phoenix_canarensis.csv
183.80 KB
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Distance_Kinship_Matings_Prunus_lannesiana.csv
110.44 KB
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Distance_Kinship_Matings_Sorbus_domestica.csv
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Abstract
Assortative mating is a deviation from random mating based on phenotypic similarity. As it is much better studied in animals than in plants, we investigate for trees whether kinship of realized mating pairs deviates from what is expected from the set of potential mates and use this information to infer mating biases that may result from kin recognition and/or assortative mating. Our analysis covers twenty species of trees for which microsatellite data is available for adult populations (potential mates) as well as seed arrays. We test whether mean relatedness of observed mating pairs deviates from null expectations that only take pollen dispersal distances into account (estimated from the same dataset). This allows to identify elevated as well as reduced kinship among realized mating pairs, indicative of positive and negative assortative mating, respectively. The test is also able to distinguish elevated biparental inbreeding that occurs solely as a result of related pairs growing closer to each other from further assortativeness.
Assortative mating in trees appears potentially common but not ubiquitous: nine data sets show mating bias with elevated inbreeding, nine do not deviate significantly from the null expectation, and two show mating bias with reduced inbreeding.
While our datasets lack direct information on phenology, our investigation of the phenological literature for each species identifies flowering phenology as a potential driver of positive assortative mating (leading to elevated inbreeding) in trees. Since active kin recognition provides an alternative hypothesis for these patterns, we encourage further investigations on the processes and traits that influence mating patterns in trees.
Methods
For all data sets we calculated pairwise kinship coefficients (Fij, Loiselle et al. 1995) and pairwise geographic distances for all adult trees, using software SPAGeDi 1-5a (Hardy and Vekemans 2002). Paternity assignments were conducted with Cervus 3.0.7 (Marshall et al. 1998; Kalinowski et al. 2007).