Spatial variation in carotenoid plumage coloration and relationships between female coloration and quality in Prothonotary Warblers (Protonotaria citrea)

The Auk ◽  
2019 ◽  
Vol 136 (2) ◽  
Author(s):  
Morgan C Slevin ◽  
Lesley P Bulluck ◽  
Alix E Matthews ◽  
Than J Boves

Abstract Many birds use conspicuous plumage coloration to signal quality for sexual or social selection. However, it is still often unclear how intraspecific coloration and associated signaling vary spatially. Plumage coloration that is dependent on carotenoids may be ideal for studying spatial color variation because birds cannot naturally synthesize this pigment; therefore, bird coloration from carotenoids is at least partially contingent upon diet. As food availability often varies spatially, so might color and its signaling strength. While male coloration has received more research focus, less is known about female coloration and its relationships with social rank or sexual quality. To further improve our understanding of spatial variation in plumage coloration and correlations with individual quality, we compared Prothonotary Warblers breeding at 2 ecologically disparate sites separated by 1,300 km: in bottomland forests of Arkansas, USA, and the forests near the tidal freshwater James River in Virginia, USA. We assessed crown and breast plumage coloration for both sexes and compared several color metrics between sites. We then assessed surrogates of female quality (number of young fledged, number of eggs laid, provisioning rate, apparent annual survival, and nest depredation) and compared coloration-quality relationships between sites. We found that coloration of birds breeding in Arkansas was generally more elaborate than those breeding in Virginia. However, this was somewhat dependent on sex: females showed greater differences than males between sites. Additionally, color metrics of females breeding in Virginia showed stronger relationships with quality (all 5 quality metrics) than for birds breeding in Arkansas (only provisioning rate and nest depredation). Proximately, spatial variation in plumage coloration and the associated signaling may be explained by differences in diet between sites. Ultimately, spatial variation in intra- and intersexual selection pressures may explain how spatial variation in plumage signal strength evolved.

The Auk ◽  
2017 ◽  
Vol 134 (1) ◽  
pp. 229-239 ◽  
Author(s):  
Lesley P. Bulluck ◽  
Miran J. Foster ◽  
Samantha Kay ◽  
Donald E. Cox ◽  
Catherine Viverette ◽  
...  

The Condor ◽  
2007 ◽  
Vol 109 (1) ◽  
pp. 187-192 ◽  
Author(s):  
Ana S. Barreira ◽  
Dario A. Lijtmaer ◽  
Stephen C. Lougheed ◽  
Pablo L. Tubaro

Abstract Abstract Ultramarine Grosbeaks (Cyanocompsa brissonii) possess a striking sexual dichromatism, with males dark blue and females brown. There are two subspecies in Argentina: the larger-bodied C. b. argentina, which is common in shrubs and semiopen areas, and the smaller C. b. sterea that inhabits forests. We measured reflectance spectra of six plumage patches from study skins to evaluate the possibility of color differences between males of each subspecies and temporal variation in plumage coloration. We found differences between subspecies in color brightness, hue, saturation, and UV chroma in the plumage patches of more conspicuous coloration, which could be related to ambient light differences between the environments that each subspecies inhabits. We also documented temporal color variation in some plumage patches, in particular a gradual decrease of UV reflectance and a gradual increase in hue after molting, possibly attributable to feather wear.


2011 ◽  
Vol 61 (4) ◽  
pp. 441-455 ◽  
Author(s):  
Adrian Surmacki

AbstractPlumage coloration is an important trait used by birds in mate choice decisions and is often an indicator of social status. The two main types of color-producing mechanisms in feathers are pigment deposition (pigmentary coloration) or the coherent scattering of light reflected from keratin microstructure (structural coloration). External factors acting on the feather surface are also hypothesized to affect structural coloration. Because preening is an energy and time demanding behavior, color variation caused by soiling deposition is generally assumed to strengthen the condition signaling function of plumage coloration. To date, studies using artificial soiling have confirmed those hypotheses. However, information about how natural soiling affects plumage color are still scarce. In this paper, I investigated the effect of natural soiling on structurally-based feather color of blue tits Cyanistes caeruleus. As a method, I applied mechanical cleaning that functionally mimicked natural preening. Removal of soiling caused a decrease of ultraviolet (UV) chroma in males and decrease in brightness in females. According to visual contrast modeling, only changes in brightness should be perceived by birds. Further, more efficient chemical cleaning resulted in a significant increase in brightness in both sexes, presumably due to preen wax removal. These results suggest that the impact of natural feather soiling is not likely to modify structural coloration signaling. One possible explanation is that, under natural conditions, the amount of soil accumulating on feathers is too small to affect coloration.


Author(s):  
Delbert E. Philpott ◽  
W. Sapp ◽  
C. Williams ◽  
T. Fast ◽  
J. Stevenson ◽  
...  

Space Lab 3 (SL-3) was flown on Shuttle Challenger providing an opportunity to measure the effect of spaceflight on rat testes. Cannon developed the idea that organisms react to unfavorable conditions with highly integrated metabolic activities. Selye summarized the manifestations of physiological response to nonspecific stress and he pointed out that atrophy of the gonads always occurred. Many papers have been published showing the effects of social interaction, crowding, peck order and confinement. Flickinger showed delayed testicular development in subordinate roosters influenced by group numbers, social rank and social status. Christian reported increasing population size in mice resulted in adrenal hypertrophy, inhibition of reproductive maturation and loss of reproductive function in adults. Sex organ weights also declined. Two male dogs were flown on Cosmos 110 for 22 days. Fedorova reported an increase of 30 to 70% atypical spermatozoa consisting of tail curling and/or the absence of a tail.


1966 ◽  
Author(s):  
Henriette Groot ◽  
Evelyn Crumpton ◽  
Harry M. Grayson
Keyword(s):  

2019 ◽  
Author(s):  
Joel L Pick ◽  
Nyil Khwaja ◽  
Michael A. Spence ◽  
Malika Ihle ◽  
Shinichi Nakagawa

We often quantify a behaviour by counting the number of times it occurs within a specific, short observation period. Measuring behaviour in such a way is typically unavoidable but induces error. This error acts to systematically reduce effect sizes, including metrics of particular interest to behavioural and evolutionary ecologists such as R2, repeatability (intra-class correlation, ICC) and heritability. Through introducing a null model, the Poisson process, for modelling the frequency of behaviour, we give a mechanistic explanation of how this problem arises and demonstrate how it makes comparisons between studies and species problematic, because the magnitude of the error depends on how frequently the behaviour has been observed (e.g. as a function of the observation period) as well as how biologically variable the behaviour is. Importantly, the degree of error is predictable and so can be corrected for. Using the example of parental provisioning rate in birds, we assess the applicability of our null model for modelling the frequency of behaviour. We then review recent literature and demonstrate that the error is rarely accounted for in current analyses. We highlight the problems that arise from this and provide solutions. We further discuss the biological implications of deviations from our null model, and highlight the new avenues of research that they may provide. Adopting our recommendations into analyses of behavioural counts will improve the accuracy of estimated effect sizes and allow meaningful comparisons to be made between studies.


2006 ◽  
Vol 7 (2) ◽  
pp. 181-188 ◽  
Author(s):  
A. Altobelli ◽  
E. Bressan ◽  
E. Feoli ◽  
P. Ganis ◽  
F. Martini

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