From: Intrinsic differences between males and females determine sex-specific consequences of inbreeding
Species | Vulnerable sex | Traits examined | Conclusions | Reference |
---|---|---|---|---|
Wild gourd | Female | Fruit and flower number, seed germination, pollen success | Female function requires more resources than male function | [53] |
Morning glory | Female | Flower and seed number, survival | Different numbers of loci affecting fitness or different average contributions | [67] |
Drosophila | Male | Larval-adult survival, female fecundity, male mating success | Inclusion of the opportunity for male-male competition increases differences in inbreeding depression among sexes | [11] |
Drosophila | Male | Egg hatchability, larval-adult survival, female fecundity, male mating success | Sexual selection makes inbreeding more costly for males | [7] |
Drosophila | Both | Egg-to-adult viability | No sex-specific inbreeding depression | [68] |
Stalk-eyed flies | Male/Both | Eyespan, thorax length, wing length | Sexually-selected trait (eyespan) more sensitive in males; no sex-specific differences in other traits | [69] |
Beetle | Female | Adult mortality | Sex-specific alleles involved in inbreeding depression; hemizygosity causes male-specific selection | [10] |
Beetle | Male | Sexual odorant signaling | Odorant may be male-only sexually selected trait | [70] |
Beetle | Male | Proportion of offspring in competitive environment | Males have greater reproductive variance; stressful environment amplifies inbreeding depression in males | [71] |
Butterfly | Male | Fertility | Sex-specific alleles involved in inbreeding depression; “direct or indirect fertility selection…operating differentially among the sexes” | [72] |
Hihi (bird) | Male* | Embryo/nestling mortality | Size dimorphism may increase inbreeding sensitivity; *lack of comparably inbred females may suggest elevated mortality | [73] |
Takahe (bird) | Female | Fledgling success | Sex-effect explanation “currently unknown” | [74] |
Song sparrow | Female | Offspring number and survival | Maternal effects increase female inbreeding sensitivity; reproductive ecology may decrease male sensitivity | [54] |
Song sparrow | Female/ Male/Both | Immune response (3 types) | “not clear why inbreeding effects should differ between males and females”; perhaps sex-specific variation in life-history allocation or physiology | [75] |
Japanese quail | Female | Hatching success, viability, fertility | Maternal effects; delay of sexual maturity in females | [52] |
Great tit | Both | Hatching, fledging, and breeding success | No sex-specific inbreeding depression | [76] |
Great tit | Female | Hatching success | Maternal effects increase female inbreeding sensitivity | [51] |
Zebra finch | Both/Female | Body mass, tarsus length, wing length, fat | Most morphological traits show similar patterns of inbreeding depression; sex-specific traits also vunerable | [77] |
Mouse | Male | Adult and offspring survivorship, male competitive ability | Sexual selection makes inbreeding more costly for males | [58] |
Gazelle | Female | Longevity | Longer female lifespan is more sensitive to inbreeding depression | [78] |