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Author(s):  
Crinan Jarrett ◽  
Luke L. Powell ◽  
Tabe T. Regine Claire ◽  
Melanie Tchoumbou ◽  
Barbara Helm

AbstractWood Warblers, an Afro-Palearctic migrant species, are declining steadily in Europe likely due to mortality outside their breeding grounds. However, little is known about their overwintering, and records about the sensitive life-cycle stage of moult in Africa are practically absent. To fill this gap, we report on moult of Wood Warblers captured over two winters (January–February) in 2019–2020 in Cameroon. We caught 14 individuals, of which 12 were monitored for flight feather moult. All inspected individuals showed advanced stages of flight feather renewal. Despite low sample sizes, Underhill-Zucchini moult models aptly explained variation in primary and secondary moult (R2 = 0.61). Estimated moult onset date was 26 December, completion date was 25 February, and moult duration was 61 days. These findings fit well with experimental data on the annual cycle and the timing of recently published migration tracks of Wood Warblers. Jointly, the data suggest that moult timing is set by an internal programme, which enables Wood Warblers to organise their multi-stage migration such that they reach suitable moulting habitat in time, and can depart in time with a fresh plumage for the breeding grounds. In our study, moult occurred during the peak of the dry season, which in Cameroon nonetheless shows high relative humidity. During our mist-netting on 28 cocoa plantations of varying shade cover, Wood Warblers were caught on 6 farms whose canopies were comparatively open. These data suggest that the birds encounter in Cameroon relatively stable climatic conditions for moult, and do not measurably prefer closed-canopy forests. Our findings are important, because successful moult increases survival prospects and because moult needs to be safely embedded in a migratory life cycle. Hence, information on moult timing and location is essential for identifying year-round vulnerabilities of Wood Warblers.


The Auk ◽  
2021 ◽  
Vol 138 (1) ◽  
Author(s):  
Ronald L Mumme ◽  
Robert S Mulvihill ◽  
David Norman

Abstract Rapid high-intensity molt of flight feathers occurs in many bird species and can have several detrimental consequences, including reductions in flight capabilities, foraging performance, parental care, and plumage quality. Many migratory New World warblers (family Parulidae) are known to have intense remigial molt, and recent work has suggested that simultaneous replacement of the rectrices may be widespread in the family as well. However, the phylogenetic distribution of simultaneous rectrix molt, and high-intensity flight feather molt more generally, has not been systematically investigated in warblers. We addressed this issue by examining flight feather molt in 13 species, representing 7 different warbler genera, at Powdermill Avian Research Center in southwestern Pennsylvania, USA. All 13 species replaced their 12 rectrices simultaneously, with the onset of rectrix molt occurring in the early-middle stages of high-intensity primary molt. As expected, single-brooded early migrants molted earlier than double-brooded species whose nesting activities extend into late summer. However, our finding that late-molting species replaced their primaries more slowly and less intensively than early molting species was unexpected, as late-molting species are widely hypothesized to be under stronger migration-related time constraints. This surprising result appears to be at least partially explained by a positive association between the pace of molt and daylength; shorter late-summer days may mandate reduced daily food intake, lower molt intensity, and a slower pace of molt. In comparison to other passerines, flight feather molt in warblers of eastern North America is extraordinarily intense; at its peak, individuals are simultaneously replacing 50–67% of their 48 flight feathers (all 12 rectrices and 6–10 remiges on each wing) for 2–3 weeks or more. Because molt of this intensity is likely to present numerous challenges for flight, avoiding predators, foraging, and parental care, the period of flight feather molt for warblers constitutes a highly demanding phase of their annual cycle.


2020 ◽  
Author(s):  
Di Tang ◽  
Dawei Liu ◽  
Yin Yang ◽  
Yang Li ◽  
Xipeng Huang ◽  
...  
Keyword(s):  

The Auk ◽  
2020 ◽  
Vol 137 (4) ◽  
Author(s):  
Sievert Rohwer ◽  
Vanya G Rohwer ◽  
Meera Lee Sethi ◽  
Janneke HilleRisLambers

Abstract Using the patterns of fault bars in their primaries, we studied the mode of primary replacement in non-molting Lesser Sandhill Cranes (Antigone c. canadensis) salvaged from hunters in southwestern Saskatchewan. About 80% of their primaries are used for 2 yr and 20% for 3 yr. Primaries are replaced during the breeding season and are lost in synchronous blocks representing about half the primaries, suggesting that most adults probably can fly weakly during flight feather replacement. Cranes are large, aggressive birds, and this interesting, and undescribed mode of flight feather replacement seems adapted to the ability of adult cranes to defend their precocial chicks from predators. Strikingly, juvenile Sandhill Cranes showed no fault marks in their primaries, suggesting that their parents’ ability to protect them shields them from the fright of predator attacks, which, in most birds, causes fault bars to be more prevalent and strongly expressed in juveniles than adults. Adults show interesting variation in the number of primaries replaced annually, which seems likely related to whether or not they are caring for chicks. Further, single primaries may or may not be replaced preferentially, suggesting sensitivity to feather function. Evaluating these observations must await field studies of molting adults.


Development ◽  
2020 ◽  
Vol 147 (9) ◽  
pp. dev188821
Author(s):  
Lara Busby ◽  
Cristina Aceituno ◽  
Caitlin McQueen ◽  
Constance A. Rich ◽  
Maria A. Ros ◽  
...  

2020 ◽  
Author(s):  
Steven J. Portugal ◽  
Robert L. Nudds ◽  
Jonathan A. Green ◽  
R. McNeil Alexander ◽  
Patrick J. Butler ◽  
...  

ABSTRACTFeathers act as aerodynamic cantilevers, and to withstand the prolonged cyclical loading that occurs during flight, feathers must be stiff, lightweight and strong. We experimentally tested the differences in feather structure, primarily stiffness and size, between (a) wild and captive Barnacle Geese Branta leucopsis, and (b) primary feathers dropped during the annual flight feather moult, and those feathers freshly regrown during the moult process. We found that, despite having undergone a 5,000km round-trip migration, flight feathers dropped during moult in the wild geese were stiffer than those measured in the captive geese, both for those dropped during moult and those re-grown. We propose that this may be related to diet or stress in the captive geese.


2020 ◽  
Vol 131 (4) ◽  
pp. 807
Author(s):  
Page E. Klug ◽  
H. Jeffrey Homan ◽  
Brian D. Peer ◽  
George M. Linz

Cell ◽  
2019 ◽  
Vol 179 (6) ◽  
pp. 1409-1423.e17 ◽  
Author(s):  
Wei-Ling Chang ◽  
Hao Wu ◽  
Yu-Kun Chiu ◽  
Shuo Wang ◽  
Ting-Xin Jiang ◽  
...  

2019 ◽  
Author(s):  
Lara Busby ◽  
Cristina Aceituno ◽  
Caitlin McQueen ◽  
Constance A. Rich ◽  
Maria A. Ros ◽  
...  

Flight is a triumph of evolution that enabled the radiation and success of birds. A crucial step was the development of forelimb flight feathers that may have evolved for courtship or territorial displays in ancestral theropod dinosaurs. Classical tissue recombination experiments performed in the chick embryo provide evidence that signals operating during early limb development specify the position and identity of feathers. Here we show that a positional information gradient of Sonic hedgehog (Shh) signalling in the embryonic chick wing bud specifies the pattern of adult flight feathers in a defined spatial and temporal sequence that reflects their different identities. We reveal that the Shh signalling gradient is interpreted into specific patterns of flight feather-associated gene expression. Our data suggests that flight feather evolution involved the co-option of the pre-existing digit patterning mechanism and therefore uncovers an embryonic process that played a fundamental step in the evolution of avian flight.


2019 ◽  
Vol 28 (7) ◽  
pp. 074703
Author(s):  
Di Tang ◽  
Hai Zhu ◽  
Wei Yuan ◽  
Zhongyong Fan ◽  
Mingxia Lei

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