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Journal ArticleDOI

Breeding seasonality and primary moult parameters of Euplectes species in South Africa

01 Jan 2006-Ostrich (Taylor & Francis Group)-Vol. 77, Iss: 2, pp 142-152
TL;DR: Yellow Bishops have rounder wings than other weaver species, possibly because their larger size affects flight aerodynamics, and the longer duration of primary moult of the Yellow Bishop may be related to food.
Abstract: The grassland biome in South Africa has a summer rainfall and Southern Red Bishops Euplectes orix , Fan-tailed Widows E. axillaris , White-winged Widow E. albonotatus , Red-collared Widow E. ardens and Long-tailed Widow E. progne breed from October or November to March. Primary moult starts in late March or early April. The widows with long tails (Long-tailed and Red-collared Widows) have moult durations of two months, while the widows with shorter tails (White-winged and Fan-tailed Widows) had moult durations of 1.5–1.7 months. Moult ends in late May or early June. Long-tailed Widows have rounder wings than other weaver species, possibly because their larger size affects flight aerodynamics. In the winter rainfall region, Southern Red Bishops and Yellow Bishops E. capensis start breeding after the winter rains, from August–November, and moult starts in early December. Primary moult duration in Yellow Bishops is relatively long, at 3.4 months. Yellow Bishops grow individual primary feathers at an average rate of 21.3 days per feather, while the other species moult primaries more quickly: White-winged Widow 8.1 days, Fan-tailed Widow 11.3 days, and Red-collared Widow 14.4 days. The number of primaries growing simultaneously is similar in the different species. The longer duration of primary moult of the Yellow Bishop may be related to food. Ostrich 2006, 77(3&4): 142–152

Summary (2 min read)

Jump to: [Introduction][Methods][Results] and [Discussion]

Introduction

  • There are seven breeding species of Euplectes bishops and widows in South Africa (Tarboton 2001) .
  • Species in this genus in South Africa have their distributions centred on the grassland and savanna biomes in the eastern parts of the country; Southern Red Bishops Euplectes orix and Yellow Bishops E. capensis extend into the eastern fynbos region of the Western Cape (Harrison et al.
  • This paper examines the relationship between the timing of primary moult and the timing of breeding in the annual cycles of six of the seven Euplectes species of South Africa.

Methods

  • Breeding seasonality data were obtained from the BirdLife South Africa Nest Record Card Scheme (NRC): Avian Ringing data were collected by ringers in the standard SAFRING (South African Bird Ringing Unit) electronic format.
  • The primaries were dried in an oven at 60°C for 24h to eliminate moisture and then weighed (Ohaus GA200D balance, precision 0.0001g).
  • Underhill and Joubert (1995) showed that within the Charadriiformes, the relative masses of the primary feathers were so similar that the average value for the species for which data were available could safely be used for species for which data were unavailable.
  • Presentation in tables of the statistical results of the Underhill-Zucchini moult model includes the following information: mean starting date, standard deviation of the start date, mean duration of moult, and mean completion date.
  • Thus, 95% of birds are estimated to start moult during the period from 1.96 standard deviations below the mean to 1.96 standard deviations above the mean.

Results

  • Within South Africa, breeding by Euplectes species began earliest in the Western Cape; the median date of egg laying in this province was September (Table 1 ).
  • Moulting birds were captured throughout the moulting season , sometimes in large numbers, enabling moult parameters to be estimated reliably.
  • Southern Red Bishops in the Eastern Cape showed a moult duration of 3.0 months, with moult starting in late April (Craig et al. 2001, Table 3 ).
  • Numbers of primaries growing simultaneously were similar in the five species: Southern Red Bishop 1.7, Yellow Bishop 2.0, Fan-tailed Widow 2.2, White-winged Widow 1.9, Red-collared Widow 2.3, and Long-tailed Widow 2.2.
  • In the six Euplectes species considered, the mean starting date of primary moult was 2.5-4.3 months after the median egg laying date and 0.9-2.3 months after the 95th percentile of egg laying (Table 5 ).

Discussion

  • The rounded wing shapes of the Long-tailed Widow, compared to the Southern Red Bishop and White-winged Widow , are probably due to adaptation rather than phylogeny ( males have larger wings than females, to compensate for the aerodynamic costs of a large tail in the male (Balmford et al. 1994) .
  • Whether there is a difference in relative primary feather masses between males and females is worth investigation.
  • Seeds are probably scarcer in the fynbos habitats of the Yellow Bishop than in the grassveld occupied by the other Euplectes species; it is therefore not unexpected that the duration of moult of the Yellow Bishop is c. 65% longer than the average of the species in summer rainfall areas (Table 3 ).
  • It would be beneficial to obtain moult records for the Yellow Bishop from other parts of their range, to understand how the timing and duration of moult is adjusted in different environmental regions.
  • The delay between the end of breeding and start of primary moult varied from 0.9-1.7 months.

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Citations
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Journal ArticleDOI
TL;DR: In this paper, the authors investigated bird nest predation using artificial nests in urban areas of the KwaZulu-Natal (KZN) Province of South Africa from June 2013 through February 2014.
Abstract: As urbanization increases, the identification of nest predators becomes important for avian conservation and management of urban wildlife communities. We investigated bird nest predation using artificial nests in urban areas of the KwaZulu-Natal (KZN) Province of South Africa. From June 2013 through February 2014 we installed seventy-five artificial nests in 25 suburban gardens in the Ethekwini and Msunduzi municipalities of KZN. Euplectes spp. nests were used and baited with two quail-sized, hand-made, silicon eggs. These were placed in residential gardens and monitored by camera traps for 2-weeks in winter, spring and summer respectively. Generally bird nesting occurs throughout the year in KZN’s subtropical climate, with some avoidance during the autumn season. Therefore, experiments were not conducted during autumn, as fresh nests were not available for use. Overall the rate of predation on artificial nests was 25 % (n = 19), with vervet monkeys Ceropithecus aethiops pygerythrus predating 20 % (n = 17) of the nests while domestic cats Felis catus predated 3 % (n = 2) of nests. Nest predation was significantly higher in the winter season, with 79 % of depredations occurring in winter (n = 15), 16 % in spring (n = 3) and 5 % in summer (n = 1), and in areas with less canopy cover. Our results suggest that vervet monkeys may have a negative impact on nesting birds in urban environments, however, in order to assess the rate of predation experiments on natural nests coupled with information on fledgling success is deemed necessary to investigate avian population declines.

25 citations


Cites background from "Breeding seasonality and primary mo..."

  • ...occurs throughout the year in KZN’s subtropical climate, with some avoidance of nesting during the autumn season (Oschadleus and Underhill 2006)....

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  • ...Generally bird nesting occurs throughout the year in KZN’s subtropical climate, with some avoidance of nesting during the autumn season (Oschadleus and Underhill 2006)....

    [...]

Journal ArticleDOI
01 Jul 2019-Ibis
TL;DR: It is suggested that because environmental conditions permit year‐round breeding, and because reproductive output is subject to high predation risk, there is probably a weak selection for individuals to match breeding with variable peak conditions in the environment.
Abstract: In some tropical birds, breeding seasonality is weak at the population level, even where there are predictable seasonal peaks in environmental conditions. It therefore remains unclear whether individuals are adapted to breeding at specific times of the year or flexible to variable environmental conditions. We tested whether the relative year‐round breeding activity of the Common Bulbul Pycnonotus barbatus arises due to within‐individual variability in breeding dates. We collected data from 827 birds via mist‐netting over 2 years with corresponding local weather data. We used a combination of climate envelope and generalized linear mixed models to explore how the timing of breeding is influenced by time of year, individual variation, rainfall and temperature in a West African savannah where seasonal precipitation determines annual variation in environmental conditions. We also pooled 65 breeding records from 19 individuals recorded between 2006 and 2017 based on brood patch occurrence and behavioural observation to compare within‐individual and population variability in breeding dates. We show that the breeding dates of individuals may be as variable as for the population as a whole. However, we observed a seasonal peak in juvenile occurrence that varies significantly between years. Models suggest no relationship between nesting and moult, and within‐year variation in rainfall and temperature, and birds were unlikely to breed during moult but may do so afterwards. Moult was very seasonal, correlating strongly with day length. We suggest that because environmental conditions permit year‐round breeding, and because reproductive output is subject to high predation risk, there is probably a weak selection for individuals to match breeding with variable peak conditions in the environment. Instead, moult, which always occurs annually and successfully, is probably under strong selection to match variable peak conditions in the environment so that long‐term survival ensures future reproduction.

11 citations


Cites background from "Breeding seasonality and primary mo..."

  • ...More recent studies (Dittami &Gwinner 1985, Tye 1992, Oschadleus & Underhill 2006, Greeney 2010, Reynolds et al. 2014), however, have revealed that breeding strategies are diverse and closely related to species niche, albeit with exceptions such as Ndithia et al. (2017) who found no relationship…...

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Journal ArticleDOI
08 Jul 2010-Ostrich
TL;DR: It is suggested that sex, geographical area and possible annual environmental variations may all influence the timing of moult in local populations of Southern Red Bishops Euplectes orix in relation to sex and geographical region.
Abstract: Using the SAFRING database and the Underhill-Zucchini model of primary moult, we analysed the timing of wing moult in Southern Red Bishops Euplectes orix in relation to sex and geographical region. Birds from the winter rainfall region in the south-western sector of the Western Cape start the annual moult more than two months before any other population, but there were no significant differences in starting date within the summer rainfall region. There were striking differences in the estimates of moult duration (62–114 d), which did not follow a consistent pattern in relation to sex or geography; annual variation within a region may be an additional factor. Throughout southern Africa, both sexes showed a trend for longer-winged birds to take more time to complete their moult. We suggest that sex, geographical area and possible annual environmental variations may all influence the timing of moult in local populations. In this sexually dimorphic species, males are consistently longer-winged and heavier tha...

10 citations

Journal ArticleDOI
31 Mar 2010-Ostrich
TL;DR: Investigation of the differences in the timing and duration of primary wing moult between males and females of sexually dimorphic passerines from the Western Cape, South Africa found variations in the patterns of moult were discussed in the context of differences in parental care.
Abstract: SAFRING ringing data was used to investigate the differences in the timing and duration of primary wing moult between males and females of sexually dimorphic passerines from the Western Cape, South Africa. In the sunbirds, weavers and canaries that were considered, the males generally started moult before the females, whereas this was not so for other species. In the species where males started moult before the females, the standard deviation of the start of moult was generally smaller in the males and the males generally took longer to moult. These differences in the patterns of moult are discussed in the context of differences in parental care between males and females of each species and within their taxonomic groups. OSTRICH 2010, 81(1): 63–67

9 citations

DissertationDOI
14 Jun 2019
TL;DR: Environmental conditions affect immune function more directly than via resource allocation trade-offs, but that variation in immune function does not follow simple environmental productivity pattern.
Abstract: "My studentship was supported by the Leventis Conservation Foundation through the University of St. Andrews, an Ubbo Emmius grant from the University of Groningen, a Royal Netherlands Academy of Arts and Science (KNAW) Academy Ecology Fund and an A. G. Leventis Foundation grant." -- Acknowledgements

7 citations


Cites background from "Breeding seasonality and primary mo..."

  • ...More recent studies (Dittami and Gwinner 1985, Tye 1992), Oschadleus and Underhill 2006, Greeney 2010, Reynolds et al. 2014) revealed however, that breeding strategies are diverse and closely related to species niche, albeit with exceptions such as Ndithia et al. (2017) who found no relationship…...

    [...]

References
More filters
Book
01 Jan 1997
TL;DR: In this paper, a major work covering the breeding and non-breeding birds of the Southern African sub-region is presented, which sets new standards in its scope and in its methods, for setting a measured baseline against which to judge environmental trends across the great range of southern Africa.
Abstract: This is a major work covering the breeding and non-breeding birds of the Southern African sub-region. Published in two volumes, Volume One includes introductory chapters describing methodology and the 'avi'-geography of the region, with habitat photos, and coverage of the non-passerines, whilst Volume Two covers the passerines. Some 900 species are covered in total, including 200 vagrants, with detailed species accounts, maps and statistics for at least 500 species. Conservation issues are discussed for most species. '...sets new standards in its scope and in its methods...it will come to be valued ever more as years go by, for setting a measured baseline against which to judge environmental trends across the great range of southern Africa.' - Colin Bibby, "BirdLife International".

347 citations

Book
01 Jan 1997

171 citations


"Breeding seasonality and primary mo..." refers background in this paper

  • ...Six species occur in Limpopo Province, Gauteng and the Eastern Cape; five species occur in the North-west and Free State Provinces; three species occur in the Western Cape; and three species have been recorded in the Northern Cape....

    [...]

  • ...Breeding of Red Bishops and Yellow Bishops in the Western Cape takes place at this time of the year....

    [...]

  • ...…in this genus in South Africa have their distributions centred on the grassland and savanna biomes in the eastern parts of the country; Southern Red Bishops Euplectes orix and Yellow Bishops E. capensis extend into the eastern fynbos region of the Western Cape (Harrison et al. 1997, Figure 1)....

    [...]

  • ...Species in this genus in South Africa have their distributions centred on the grassland and savanna biomes in the eastern parts of the country; Southern Red Bishops Euplectes orix and Yellow Bishops E. capensis extend into the eastern fynbos region of the Western Cape (Harrison et al. 1997, Figure 1)....

    [...]

  • ...Copyright © NISC Pty Ltd OSTRICH EISSN 1727–947X The grassland biome in South Africa has a summer rainfall and Southern Red Bishops Euplectes orix, Fan-tailed Widows E. axillaris, White-winged Widow E. albonotatus, Red-collared Widow E. ardens and Long-tailed Widow E. progne breed from October or November to March....

    [...]

Journal ArticleDOI
03 Apr 2008-Ibis
TL;DR: In this paper, the authors present a new approach to the analysis of primary moult and develop a mathematical model specifically designed for moult data, which is based on regression methods commonly used to estimate the parameters associated with moult in birds.
Abstract: The regression methods frequently used to estimate the parameters associated with primary moult in birds are unsatisfactory. Results obtained using least squares regression, and various ad hoc adaptations, are so obviously incorrect that many authors have fitted lines ‘by eye’ (Newton 1968, Thomas & Dartnall 1971, Elliott et al. 1976, Morrison 1976, Appleton & Minton 1978). In a comparison of seven regression methods, estimates of the average starting date varied between 29 June and 31 July, completion date between 2 and 24 October, and duration of moult between 72 and 109 days for the Redshank Tringa totanus, in spite of the very large sample of 1482 observations (Summers et al. 1983). In this paper we present a new approach to the analysis of primary moult and develop a mathematical model specifically designed for moult data.

159 citations


"Breeding seasonality and primary mo..." refers background or methods in this paper

  • ...For each species, a geographic area was chosen, so that sufficient records could be obtained for the analysis of moult: generally, 200 records spread over a year are adequate to enable the moult model of Underhill and Zucchini (1988) to converge....

    [...]

  • ...The data were considered to be of ‘Type 2’ of Underhill and Zucchini (1988), because full moult scores were recorded for each bird and all birds were considered to be available for sampling throughout the moult period....

    [...]

  • ...The UnderhillZucchini moult model (Underhill and Zucchini 1988) was used to estimate the parameters of primary moult....

    [...]

Journal ArticleDOI
01 Jul 2003-Ibis
TL;DR: It was found that level flapping-flight speed and the ability to negotiate an aerial obstacle course were unrelated to wingtip shape, but take-off parameters did vary with wing Tip shape; birds with more rounded wingtips tended to take off from the ground at a steeper angle of ascent than those with relatively more pointed wingtips.
Abstract: Although wingform is known to differ among individuals of the same species it is not known how intraspecific variation in wingtip shape is associated with flight performance. In this study, we have examined both among- and within-individual variation in wingtip shape in relation to changes in flight performance in the European Starling Sturnus vulgaris . We found that level flapping-flight speed and the ability to negotiate an aerial obstacle course were unrelated to wingtip shape. However, take-off parameters did vary with wingtip shape; birds with more rounded wingtips tended to take off from the ground at a steeper angle of ascent than those with relatively more pointed wingtips. The same relationships between wingtip morphology and flight were present in both the inter- and intra-individual experimental analyses. The evolutionary importance of this variation in take-off ability is discussed in terms of predator avoidance and enhancement of individual survival.

88 citations


"Breeding seasonality and primary mo..." refers background in this paper

  • ...European Starlings Sturnus vulgaris, with rounded wings, are able to take off from the ground at a steeper angle of ascent than those species with relatively more pointed wingtips (Swaddle and Lockwood 2003)....

    [...]

  • ...European Starlings Sturnus vulgaris, with more rounded wingtips, tended to take off from the ground at a steeper angle of ascent than those with relatively more pointed wingtips (Swaddle and Lockwood 2003)....

    [...]

Journal ArticleDOI
TL;DR: The findings confirm that certain aspects of sexual dimorphism may sometimes have evolved through selection for traits that reduce the costs of elaborate sexually selected characters, and suggest that future work aimed at understanding sexual selection by investigating patterns of sexualDimorphism should attempt to differentiate between the direct and indirect consequences of sexual selection.
Abstract: Recent work on birds suggests that certain morphological differences between the sexes may have evolved as an indirect consequence of sexual selection because they offset the cost of bearing extravagant ornaments used for fighting or mate attraction. For example, long-tailed male sunbirds and widowbirds also have longer wings than females, perhaps to compensate for the aerodynamic costs of tail elaboration. We used comparative data from 57 species to investigate whether this link between sexual dimorphism in wing and tail length is widespread among long-tailed birds. We found that within long-tailed families, variation in the extent of tail dimorphism was associated with corresponding variation in wing dimorphism. One nonfunctional explanation of this result is simply that the growth of wings and tails is controlled by a common developmental mechanism, such that long-tailed individuals inevitably grow long wings as well. However, this hypothesis cannot account for a second pattern in our data set: as predicted by aerodynamic theory, we found that, comparing across long-tailed families, sexual dimorphism in wing length varied with tail shape as well as with sex differences in tail length. Thus, wing dimorphism was generally greater in species with aerodynamically costly graduated tails than in birds with cheaper, streamer-shaped tails. This result was not caused by confounding phylogenetic effects, because it persisted when phylogeny was controlled for, using an independent comparisons method. Our findings therefore confirm that certain aspects of sexual dimorphism may sometimes have evolved through selection for traits that reduce the costs of elaborate sexually selected characters. We suggest that future work aimed at understanding sexual selection by investigating patterns of sexual dimorphism should attempt to differentiate between the direct and indirect consequences of sexual selection.

72 citations


"Breeding seasonality and primary mo..." refers background in this paper

  • ...The mean tail lengths of male and female Long-tailed Widows are 411mm and 62mm, respectively (Hockey et al. 2005); males have larger wings than females, to compensate for the aerodynamic costs of a large tail in the male (Balmford et al. 1994)....

    [...]

Frequently Asked Questions (6)
Q1. What contributions have the authors mentioned in the paper "Breeding seasonality and primary moult parameters of euplectes species in south africa" ?

In a recent study, Ostrich et al. this paper found that the primary moult duration of the Southern Red and Yellow Bishops is relatively long, at 3.4 months. 

Adult Yellow Bishops needed 2–4 weeks to grow individual primaries, while the other species moulted individual primaries more quickly. 

They estimated duration of moult to be 110 days in Southern Red Bishops, 100 days in male Fan-tailed Widows, and 80 days for Red-collared Widows and female Fan-tailed Widows. 

The mean tail lengths of male and female Long-tailed Widows are 411mm and 62mm, respectively (Hockey et al. 2005);males have larger wings than females, to compensate for the aerodynamic costs of a large tail in the male (Balmford et al. 1994). 

The data were considered to be of ‘Type 2’ of Underhill and Zucchini (1988), because full moult scores were recorded for each bird and all birds were considered to be available for sampling throughout the moult period. 

For Long-tailed Widows, 279 moult records were available (166 records for Mpumulanga, 55 for the Free State, 53 for Gauteng, and five records from other provinces).