Flight-Feather Molt Patterns and Age in North American Owls Peter Pyle

The Auk ◽  
1998 ◽  
Vol 115 (2) ◽  
pp. 553-553
Author(s):  
Jonathan Dwight,
PLoS Biology ◽  
2009 ◽  
Vol 7 (6) ◽  
pp. e1000132 ◽  
Author(s):  
Sievert Rohwer ◽  
Robert E. Ricklefs ◽  
Vanya G. Rohwer ◽  
Michelle M. Copple
Keyword(s):  

The Condor ◽  
2001 ◽  
Vol 103 (3) ◽  
pp. 555-569 ◽  
Author(s):  
Christopher E. Filardi ◽  
Sievert Rohwer

Abstract We describe the rules of primary flight-feather replacement for Pelagic Cormorants (Phalacrocorax pelagicus), and contrast the completeness of primary replacement in individuals from Asia and North America. In adult Pelagic Cormorants primary replacement is stepwise, with multiple waves of molt, each initiated at the innermost primary (P1), proceeding simultaneously toward the tip of the wing. Shugart and Rohwer's (1996) ontogenetic model for generating and maintaining stepwise primary replacement depended upon incomplete molts. In each new episode of molt, waves of primary replacement were thought to be initiated at P1 and at each arrested wave that had failed to replace all old feathers in the preceding molt. Because most adult Pelagic Cormorants from North America completely replace their primaries but maintain stepwise primary molts, the latter assumption must be relaxed. In contrast to the present-day situation in North America, Pelagic Cormorants from northeastern Asia have incomplete molts of their primaries, and may be forced to skip breeding in some years to clear their wings of overworn primaries. Young birds from Asia start the replacement of their juvenile primaries later than North American birds and replace more feathers simultaneously. Implicancias de la Muda Primaria Completa e Incompleta en la Historia de Vida de Phalacrocorax pelagicus Resumen. Describimos las reglas de reemplazo de plumas primarias para Phalacrocorax pelagicus y contrastamos la totalización del reemplazo de primarias entre individuos de Asia y América del Norte. En individuos adultos, el reemplazo de primarias ocurre en varias etapas, con múltiples secuencias de muda cada una iniciada en la primaria más interna (P1), procediendo simultáneamente hacia la punta del ala. El modelo ontogenético de Shugart y Rohwer (1996) para la generación y mantenimiento del reemplazo en etapas de las plumas primarias depende de mudas incompletas. Se pensaba que en cada nuevo episodio de muda las secuencias de reemplazo de primarias eran iniciadas en P1 y en cada punto de interrupción de la muda precedente que hubiera impedido el reemplazo de todas las plumas viejas. Debido a que la mayoría de los individuos adultos de P. pelagicus de Norteamérica reeemplazan completamente sus primarias pero aún lo hacen en etapas, la última suposición debe ser re-evaluada. En contraste con la situación actual en Norteamérica, individuos del noreste de Asia tienen mudas incompletas de sus primarias y pueden verse forzados a no reproducirse en algunos años para despojarse de la presencia de primarias desgastadas. Las aves juveniles de Asia comienzan el reemplazo de sus primarias más tarde y reemplazan más plumas simultáneamente que las aves de Norteamérica.


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.


Ornis Svecica ◽  
2011 ◽  
Vol 21 (1) ◽  
pp. 11-19
Author(s):  
Roar Solheim

Great Grey Owls start flight feather moult when in their second year. Moult was studied on outspread wings of 58 individuals in the collections at Naturhistoriska Riksmuseet in Stockholm. The owls always moulted the innermost secondaries in their first moult, and usually at least two primaries, most often P5 and P6. After this moult, birds had 11–17 juvenile feathers left in each wing, of a total of 21 flight feathers. In their second flight feather moult, birds shed primaries outwards and inwards from the primaries moulted during the first moult. A variable number of secondaries outwards from S10 and S11 were moulted. All birds retained at least one juvenile feather, always P1. The number of juvenile flight feathers after the second moult was 1–6. The collection held no individuals known to be in their third flight feather moult. Thus it was not possible to determine whether birds in this age group could be aged by the wing moult pattern. Great Grey Owls with no juvenile flight feathers should thus be classified as 4C+ in autumn, and 5C+ in spring.


The Condor ◽  
2006 ◽  
Vol 108 (4) ◽  
pp. 877-886 ◽  
Author(s):  
Guillermo E. Pérez ◽  
Keith A. Hobson

Abstract Abstract The Loggerhead Shrike (Laniusludovicianus) breedsthroughout North America and various populationsapparently exhibit diverse molt strategies.However, molt in this species and how it may varygeographically is generally poorly known. Weinvestigated molt sequence in 27 breedingLoggerhead Shrikes using stable hydrogen(δD) isotope analysis of flightfeathers. Because feather δD varies with thelatitude at which feathers are grown in NorthAmerica, it is relatively straightforward toidentify those feathers grown south of anindividual's breeding location. We sampled 11feathers per individual to evaluate locations offeather molt between breeding and wintering groundsin North America. Sampling took place in centralSaskatchewan, Canada (n =  18 individuals) andin the southern region of the Saskatchewan-Manitobaborder (n =  9). We found evidencethat shrikes initiated flight feather molt on theirbreeding grounds (P1 and P3) but thenlargely suspended molt until reaching theirwintering areas. The isotopic evidence suggeststhat the first primary (P1, most depleted indeuterium, mean  = −103‰) provides information onshrike breeding latitudes while the innermosttertial (S9, most enriched in deuterium, mean =  −49‰)provides information on shrike wintering orsouthernmost molting latitudes.


The Auk ◽  
2004 ◽  
Vol 121 (1) ◽  
pp. 35-45 ◽  
Author(s):  
Christopher W. Thompson ◽  
Alexander S. Kitaysky

Abstract Previous reports have stated that Tufted Puffins (Fratercula cirrhata) lose all of their flight feathers simultaneously (or nearly so) during flight-feather molt and replace them in no apparent order. In contrast, we found that captive second-year (SY) Tufted Puffins (1) typically require 15 and 10 days to lose their primaries and secondaries, respectively, during their first flight-feather molt, and an average of 21 days to lose all of their remiges; and (2) replace their primaries in either of two discrete sequences. In 9 of 13 birds, primary molt began at the innermost primary, P1, and progressed distally to the outermost functional primary, P10. However, in the remaining four birds, primary molt began in the middle of the primaries (P5-P7) and progressed both distally to P10 and proximally toward P1. Before the proximal wave reached P1, a second wave of molt was initiated at P1 and progressed distally, typically replacing P2 and P3 before reaching the proximal wave. Such polymorphism in flight-feather molt sequence is rare in birds, having been reported previously only in a few passerine species. Secondary molt began about 13 days after onset of primary molt and finished at about the same time as primary molt, resulting in a total duration of flight-feather molt of ∼54 days and a flightless period of ∼40 days.


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

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