Castor is an industrially important oilseed crop. Vascular wilt caused by the soil borne fungus Fusarium oxysporum f. sp. ricini is a serious disease of castor. Use of resistant cultivars is the only viable option for management of wilt disease problem in castor production. Excellent sources of resistance to wilt have been found in castor germplasm. In this study, a set of four castor inbred lines (48–1, CI-1, AP42 and AP48) was characterized for inheritance of resistance to wilt by studying segregating populations generated by crossing these inbred lines with eight different susceptible genotypes. An artificial screening method (sick pot) with a new scoring system (days to wilt) was used for evaluation of plant progenies for reaction to the pathogen infection. The reaction of F1s indicated that the nature of resistance in 48–1, CI-1 and AP48 is recessive whereas it was dominant in AP42. Inheritance results from eight F2 populations showed that resistance to wilt is conferred by a single locus in one population and at least two loci, which interact in complementary way, in other seven populations. Different modes of inheritance were also observed when the same resistant source was crossed with different susceptible parents, indicating the possible role of genetic backgrounds in determining resistance. Overall, the results suggested that Mendelian resistance to wilt is predominant in the castor genotypes, which can be exploited for breeding cultivars. Particularly, AP42 with dominant nature of resistance will be of great interest to hybrid breeding.

Village chickens have been kept for millennia under patronage of smallholder farmers. Our study was intended at dissecting the signature of artificial selection and ecological variation on morphological structures of Ethiopian village chickens. This report was based on visual traits of 798 chickens and a concise one-to-one interview of 399 farmers for their preferences on chicken morphology. Significant population-specific differences in morphological counts were commonly found for rare morphological variants. Most of them were frequently seen in Jarso chickens, while some of them unique to Jarso chickens. This might be explained by the effect of location-specific evolutionary forces and differences in their breeding histories. The high within population variation in the frequency of morphological counts was observed among these panmictic chicken populations largely evolved under uncontrolled mating. Single comb was not (less) preferred by majority of the farmers (93.8 percent); it was thus present at a low frequency (26.7 percent). Farmers have shown high preference for yellow shank (42.3 percent), which was then frequently observed (61.1 percent). The reported reasons for morphological likeness were visual appeal, market demand and cultural and religious values. The absence of significant variation in preferences for chicken morphology among communities between the two study sites was attributed to their multifunctional needs.

The 20th Century saw an astonishing advance in our understanding of genetics and the scientific basis of the genetic improvement of farm animals. The application of genetic principles to chickens in the 1950s and 1960s led to a rapid change in the productivity and efficiency of laying hens and broiler chickens, turkeys and ducks. Subsequently, the application of increasingly powerful computers and sophisticated mathematical algorithms has increased the range of traits that could be successfully incorporated into breeding programs. Random sample tests of the performance of laying hens enjoyed a period of popularity and more recently the few remaining tests included husbandry systems in addition to strain evaluation. Characterisation of avian blood groups has led to the identification of the B21 haplotype that confers resistance to Marek's disease and to selection for this locus in commercial lines. The decade following the millennium saw the publication of the genome sequence of the chicken and the identification of millions of single nucleotide polymorphisms that, coupled with technological advances, made the application of whole genome selection practical in poultry. In parallel, the molecular basis for some Mendelian traits described a century ago is now being deciphered. Similar technologies have been applied to study genetic diversity in chickens and have provided insights into the evolution and domestication of chicken breeds. Finally, in this review, the recent development of the European Poultry Genetics Symposia coordinated by Working Group 3 ‘Genetics and Breeding’ that was based on combining the British Poultry Breeders Round Table and AVIAGEN from West and Eastern Europe, is discussed.

La palourde japonaise présente un grand polymorphisme de coloration de la coquille. Bien que ce polymorphisme soit connu depuis longtemps, son hérédité n'a jamais été analysée. Cette étude a pour but, hormis la connaissance fondamentale du déterminisme génétique des caractères de la coloration, de permettre de produire des individus homozygotes pour la coloration. Ceux-ci pourront être utilisés comme marqueurs génétiques dans des expériences au laboratoire. La coloration est définie par trois caractères, l'asymétrie, l'ornementation et la couleur de fond. Les palourdes à coloration asymétrique sont totalement ou partiellement dépigmentées, à l'exception d'une bande postérieure sur la valve gauche. Les palourdes à coloration symétrique sont pigmentées sur les deux valves. Quatre séries de croisements ont permis l'analyse de différents caractères, Asymétrie et Symétrie, et des ornementations Vague [V] et Zébré [Z]. Les résultats suggèrent que la coloration est contrôlée par au moins deux gènes. Le caractère d'asymétrie est contrôlé par un gène à deux allèles, asymétrie (A) dominante et symétrie (S) récessive. Quelquesindividus asymétriques homozygotes ont été identifiés. Un phénotype Bigarré (Bi), est apparu dans les ségrégations du croisement V × V et des croisements Z × Z. Les résultats suggèrent que Vague et Zébré sont dominants sur Bigarré. Cependant, il existe d'autres ornementations (phénotype 1) et le gène codant pour l'ornementation serait ainsi multiallélique. Le déterminisme de la couleur n'est pas défini. Par contre, les observations montrent que la coloration n'est pas liée au sexe. Dans la majorité des croisements, les proportions observées pour l'asymétrie s'éloignent des rapports attendus selon les lois de Mendel. Cette différence est due à un déficit systématique en individus homozygotes symétriques qui n'a pu être expliqué.