plumage colour
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2022 ◽  
Author(s):  
Sean M. Mahoney ◽  
Matthew W. Reudink ◽  
Andrea Contina ◽  
Kelly A. Roberts ◽  
Veronica T. Schabert ◽  
...  

2021 ◽  
Vol 244 ◽  
pp. 105483
Author(s):  
Samuel O. Durosaro ◽  
Oluwaseun S. Iyasere ◽  
David O. Oguntade ◽  
Babatunde M. Ilori ◽  
Tejumola A. Odubola ◽  
...  

2021 ◽  
Author(s):  
Sean M Mahoney ◽  
Madison D. Oud ◽  
Claudie Pageau ◽  
Marcio Argollo de Menezes ◽  
Nathan Smith ◽  
...  

Plumage coloration is an important trait involved communication and is shaped by a variety of ecological pressures. Island residency has the potential to change the evolutionary trajectory of plumage colour by differences in habitat and resources, or by altering predation pressure and social selection intensity. Latitude, island size, and isolation may further influence colour evolution by biasing colonization. Therefore, general patterns of plumage evolution are difficult to disentangle. We used phylogenetically controlled analyses to assess the influence of island residency on plumage colouration, by calculating chromaticity values from red, blue, green scores extracted from photos of Order Passeriformes birds. Importantly, we controlled for ecological factors hypothesized to influence colour evolution and assessed family-level effects. We found 1) colour varied between islands and mainlands in females, but not males, and both sexes were affected by several ecological factors; 2) patterns of colour evolution varied among families; 3) island size and distance to the mainland and other islands significantly influenced colour; and 4) interactions between ecological factors and latitude were consistently influenced colour, supporting a latitudinal gradient hypothesis. Our results indicate although island residency influences female colour evolution, a myriad of ecological factors drive plumage colour and the patterns vary among families.


Genes ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 1097
Author(s):  
Henriëtte van der Zwan ◽  
Rencia van der Sluis

Parrots are considered the third most popular pet species, after dogs and cats, in the United States of America. Popular birds include budgerigars, lovebirds and cockatiels and are known for their plumage and vocal learning abilities. Plumage colour variation remains the main driving force behind breeder selection. Despite the birds’ popularity, only two molecular genetic tests—bird sexing and pathogen screening—are commercially available to breeders. For a limited number of species, parentage verification tests are available, but are mainly used in conservation and not for breeding purposes. No plumage colour genotyping test is available for any of the species. Due to the fact that there isn’t any commercial plumage genotype screening or parentage verification tests available, breeders mate close relatives to ensure recessive colour alleles are passed to the next generation. This, in turn, leads to inbreeding depression and decreased fertility, lower hatchability and smaller clutch sizes, all important traits in commercial breeding systems. This review highlights the research carried out in the field of pet parrot genomics and points out the areas where future research can make a vital contribution to understanding how parrot breeding can be improved to breed healthy, genetically diverse birds.


Animals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1827
Author(s):  
Enver Çavuşoğlu ◽  
Metin Petek

Transport conditions of end-of-lay hens are important for their welfare. This study investigated the effects of season, plumage colour, and transportation distance on the welfare of end-of-lay hens. Retrospective data from 31,667,274 end-of-lay hens transported to a poultry slaughterhouse in Turkey were analysed. The mean body weight loss, dead-on-arrival (DOA) rate, and reject rate were 3.723%, 1.397%, and 0.616%, respectively. The effects of season, plumage colour, and transport distance on the evaluated parameters were all statistically significant (p < 0.001). The highest body weight loss was found in winter, while the lowest body weight loss was found in autumn. The average DOA rate was highest in spring and lowest in autumn. The highest average reject rate was found in spring (0.630%). Body weight loss, DOA rates, and reject rates were also significantly different among white and brown hens (p < 0.001; p < 0.001; p = 0.016, respectively). The highest body weight loss and reject rates were found in white plumage hens, while the highest DOA rate was found in brown plumage hens. The body weight loss and DOA rate were positively correlated with transportation distance (p < 0.001). The results of this study indicate that more preventive measures should be taken during the transport of end-of-lay hens, especially in cold seasons such as winter, and over longer transport distances, in regard to the welfare of these animals. Additionally, the transport of these animals should be lessened to a certain distance.


2020 ◽  
Vol 46 (5) ◽  
Author(s):  
A. E. Jubril ◽  
T. R. Fayeye ◽  
A. A. Ademola ◽  
H. H. Gunn

This study was conducted to determine auto-sexing potential in Rhode Island, Nigerian local chicken and their reciprocal crosses. A total of 241 eggs were set in the incubator to determine the fertility, hatchability, % Hatch, % dead in shell, % dead in cell and % deformed chicks in the four genotypes (Rhode Island Red (RIR) x Rhode Island White (RIW), Rhode Island Red (RIR) x Rhode Island White (RIW), Nigerian Local Red (NLR) x Rhode Island White (RIW) and Nigerian Local Red (NLR) x Nigerian Local White (NLW). Only 94 eggs were hatched. RIRXRIW crossbred chicks had the highest percentage fertility of 88.89% followed by RIRxRIW (86.27%), NLRXRIW (77.36%) and NLRxNLW (72.31%), respectively. RIRxNLW had the highest percentage hatchability of 65.19%, followed by RIRxRIW (51.56%), NLRxNLW (51.06%) and NLRxRIW (24.39%). It was observed in the hatch-out analysis that the cross between NLRxRIW had the highest percentage of dead in shell (29.27%) followed by RIRxRIW (17.19%), NLRxNLW (17.02%) and RIRxNLW (11.36%), respectively. The highest percentage of dead in cell was recorded in NLRxRIW crossbred (43.33%), followed by NLRxNLW (31.92%), RIRxRIW (28.13%) and RIRxNLW (15.91%). The observed deformed chicks were highest in NLRxNLW (20.85%) followed by RIRxNLW (10.34%), RIRxRIW (6.06%) and NLRxNLW (0%), respectively. Also observed was the occurrence of bangers with NLRxRIW, having the highest occurrence of bangers (9.08%) and with NLRxNLW having no occurrence of bangers. The records of weekly body weight were taken on the 94 chicks and chi square analysis was used to test colour inheritance of chicks. Significant (P<0.05) difference was observed among genotypes in body weight of chicks at hatch and from weeks 1 to 8 weeks of age. The observed changes on body weight from 0 to 8th week of age of chicks showed significant difference across the four different genetic crossed groups (P<0.05) and weight at the 8th week showed that the cross between RIRxRIW (216.93g) had better in growth as compared to the cross between NLRxRIW (202.75g) and NLRxNLW (193.17g) which were statistically similar (P>0.05) and RIRxNLW (179.75g) crossbred chicks which had the lowest bodyweight at 8 weeks of age. The chi square (X2) analysis revealed that both RIRxRIW and NLRxRIW crossbred chicks were autosexed. The study concluded that selection for plumage colour showed great potential in determining the probability of chicks being autosexed. Also, pure bred of RIRXRIW and reciprocal cross of NLRXRIW showed great potential of producing autosexed chicks, while results on the direct crosses of NLRXNLW and RIRXNLW suggest that the pattern of inheritance of plumage colour is not simple. The study recommends further investigation to further ascertain the mode of plumage colour inheritance in the Nigerian Local Chickens.


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