Genetic contribution from a zoo population can increase genetic variation in the highly inbred wild Swedish wolf population

2015 ◽  
Vol 16 (6) ◽  
pp. 1501-1505 ◽  
Author(s):  
Mija Jansson ◽  
Mats Amundin ◽  
Linda Laikre
1963 ◽  
Vol 14 (1) ◽  
pp. 93 ◽  
Author(s):  
GP Davey ◽  
JSF Barker

(i) The structure and genetic history of the pedigree Hereford breed in Australia are analysed by pedigree sampling methods. (ii) The pattern of the breed structure is generally similar to that found in other breeds, but it is extremely dynamic owing to the present rapid expansion of the breed. Changes are taking place in the herd composition of the major breeders' groups and there are many new herds yet to find their level in the structure. (iii) Considerable emphasis has been placed on the use of imported animals in the development of the breed. Of all herds registering in Volume 24 of the herd book, 31.6% used imported sires, and the percentage of genes in the breed in 1949 derived from animals imported since 1880 was 97.7, and from animals imported since 1930, 53.9%. (iv) The most important herd in 1949 made a genetic contribution to the breed of 33.1%, while the contributions of the four next most important herds were 17.4, 10.1, 7.4, and 6.1%. In the four-generation pedigrees from which these figures were derived, the contribution of imported animals was 56.1%. (v) The animal with the highest relationship to the breed was Free Town Director (Imp.), with direct relationships of 5.6 and 9.2% to the 1941 and 1949 samples respectively. Of the 16 sires and one dam whose direct relationships are 3.0% or more in any of the three sample years, 12 sires were imported. (vi) The total inbreeding in 1949 (base year 1880) was 2.6%. This comprised 0.2% current inbreeding, 1.6% long-term inbreeding, and 0.8% strain inbreeding. There was no evidence of subdivision of the breed into separate strains. (vii) The effective generation length has decreased since 1930 to about 5.5 years in the 1949–50 sample. Nearly 50% of the animals in this sample were sired by bulls 4 years old or younger, while about 33% were from dams 4 years old or younger. (viii) Bulls from major breeders' herds are used widely throughout the breed, while about 90% of sires and 45% of dams were bred in herds other than the one in which they were used. Therefore, it is unlikely that there is much genetic variation between herds.


2020 ◽  
Vol 287 (1921) ◽  
pp. 20192849 ◽  
Author(s):  
Brendan P. Zietsch ◽  
Hasse Walum ◽  
Paul Lichtenstein ◽  
Karin J. H. Verweij ◽  
Ralf Kuja-Halkola

The ratio of males to females among an individual's offspring at birth (offspring sex ratio) has long been of great interest to evolutionary biologists. The human offspring sex ratio is around 1 : 1 and is understood primarily in terms of Fisher's principle (R. A. Fisher, The genetical theory of natural selection , 1930), which is based on the insight that in a population with an unequal sex ratio, each individual of the rarer sex will on average have greater reproductive value than each individual of the more common sex. Accordingly, individuals genetically predisposed to produce the rarer sex will tend to have greater fitness and thus genes predisposing to bearing that sex will increase in frequency until the population sex ratio approaches 1 : 1. An assumption of this perspective is that individuals' offspring sex ratio is heritable. However, the heritability in humans remains remarkably uncertain, with inconsistent findings and important power limitations of existing studies. To address this persistent uncertainty, we used data from the entire Swedish-born population born 1932 or later, including 3 543 243 individuals and their 4 753 269 children. To investigate whether offspring sex ratio is influenced by genetic variation, we tested the association between individuals' offspring's sex and their siblings' offspring's sex ( n pairs = 14 015 421). We estimated that the heritability for offspring sex ratio was zero, with an upper 95% confidence interval of 0.002, rendering Fisher's principle and several other existing hypotheses untenable as frameworks for understanding human offspring sex ratio.


2013 ◽  
Vol 8 (4) ◽  
pp. e42
Author(s):  
Mija Jansson ◽  
Linda Laikre ◽  
Mats Amundin ◽  
Benjamin Jöngren

2011 ◽  
Vol 49 (01) ◽  
Author(s):  
A Tönjes ◽  
A Tönjes ◽  
T Strauch ◽  
C Ruffert ◽  
J Mössner ◽  
...  

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