Flexibility in the timing of post‐breeding moult in passerines in the UK

Higher temperatures resulting from climate change have led to predictions that the duration of the breeding season of many temperate bird species may be changing. However, the extent to which breeding seasons can be altered will also depend on the degree of flexibility in processes occurring at othe...

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Published inIbis (London, England) Vol. 157; no. 2; pp. 340 - 350
Main Authors Morrison, Catriona A, Baillie, Stephen R, Clark, Jacquie A, Johnston, Alison, Leech, David I, Robinson, Robert A, Perez‐Tris, Javier
Format Journal Article
LanguageEnglish
Published Oxford Published for the British Ornithologists' Union by Academic Press 01.04.2015
Blackwell Publishing Ltd
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Summary:Higher temperatures resulting from climate change have led to predictions that the duration of the breeding season of many temperate bird species may be changing. However, the extent to which breeding seasons can be altered will also depend on the degree of flexibility in processes occurring at other points in the annual cycle. In particular, plasticity in the timing of post‐breeding moult (PBM) could facilitate changes in the timing of key events throughout the annual cycle, but little is known about the level of within‐ and between‐species plasticity in PBM. As part of the British Trust for Ornithology (BTO) Ringing Scheme, many ringers routinely record moult scores of flight feathers, and these can be used to provide information on the annual progression of PBM for a range of species. Here we use ringing data to investigate patterns of PBM in 15 passerines, as well as data from the BTO Nest Record Scheme to relate these differences to the timing of breeding of these species across the UK. We find considerable variation in both the mean start (19 May–29 July) and duration (66–111 days) of PBM between species, but find no evidence that species starting PBM later in the season complete it any faster. However, there is considerable within‐species variation in PBM, particularly for multi‐brooded species; PBM starts later and is completed in less time when the duration of the breeding season (difference between first and last nests) is longer. This implies that a later end to breeding can be compensated for by faster PBM, and that advances in breeding could lead to earlier and slower PBM. Our findings suggest that adaptation of PBM in response to climate‐mediated changes in the timing and duration of the breeding season is possible. However, the requirement to complete PBM prior to migration or the onset of winter might constrain the extent to which breeding seasons can lengthen, especially for later nesting species.
Bibliography:http://dx.doi.org/10.1111/ibi.12234
istex:1C48A03A67311CDC25D488491D08017905FC7D52
ArticleID:IBI12234
The National Parks and Wildlife Service (Ireland)
British Trust for Ornithology
ark:/67375/WNG-MKX13JZH-T
BTO Ringing and Nest Record Schemes
Data S1. Testing for the influence of phylogenetic dependence in our data. Figure S1. Frequency distribution of the change in AIC when phylogenetic dependence is included in the model structure relative to an ordinary least squares model. Table S1. The mean start date, duration and standard deviation in start date of post-breeding moult in female and male individuals of 12 species of British breeding birds.
Joint Nature Conservation Committee
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0019-1019
1474-919X
DOI:10.1111/ibi.12234