AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (499.2 KB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research | Open Access

Brood sex ratio in the Yellow-bellied Prinia (Prinia flaviventris)

Zhifeng Ding1,Fang Ji1,Qiuli Huang2Longwu Wang3Aiwu Jiang4Chunlan Zhang1Yongjun Feng1Yuan Tian1Huijian Hu1( )Wei Liang2 ( )
Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Guangdong Institute of Applied Biological Resources, Guangzhou 510260, China
Ministry of Education Key Laboratory for Tropical Plant and Animal Ecology, College of Life Sciences, Hainan Normal University, Haikou 571158, China
School of Life Sciences, Guizhou Normal University, Guiyang 550001, China
College of Forestry, Guangxi University, Nanning 530004, China

Zhifeng Ding and Fang Ji contributed equally to this work

Show Author Information

Abstract

Background

The adjustment of sex ratios in birds can occur at the egg and nestling stages. Previous studies showed that the sex ratio was affected by environmental factors and parental condition; it may result in seasonal and ecosystem differences.

Methods

In this study, the brood sex ratio of the Yellow-bellied Prinia (Prinia flaviventris) in the Nonggang area, Guangxi, southwestern China, was investigated during the breeding season from May to June in 2013 using PCR amplification from whole-genome DNA extracted from blood samples. A total of 31 nests of Yellow-bellied Prinia, including 132 brood fledglings and 31 pairs, were sampled.

Results

The results showed that the brood sex ratio of the Yellow-bellied Prinia was 1:1, and sex ratios of different nests were evenly distributed within the study area. No significant relationship was found between parental quality and nest characteristics with the brood sex ratio.

Conclusions

The present study indicated that no brood sex ratio bias in the Yellow-bellied Prinia highlighted the complexity of sex ratio adjustment in birds. In spite of our negative results, the lack of an association between brood sex ratio and parental quality and environmental factors in the Yellow-bellied Prinia provides valuable information on the adjustment of sex ratios in birds.

References

 

Barros Á, Álvarez D, Velando A. Climate influences fledgling sex ratio and sex-specific dispersal in a seabird. PLoS ONE. 2013;8:e71358.

 

Becker PH, Ezard THG, Ludwigs JD, Sauer-Gürth H, Wink M. Population sex ratio shift from fledging to recruitment: consequences for demography in a philopatric seabird. Oikos. 2008;117:60-8.

 

Bell SC, Owens IP, Lord AM. Quality of breeding territory mediates the influence of paternal quality on sex ratio bias in a free-living bird population. Behav Ecol. 2014;25:352-8.

 

Blank JL, Nolan V. Offspring sex ratio in red-winged blackbirds is dependent on maternal age. Proc Natl Acad Sci USA. 1983;80:6141-5.

 

Bouvier JC, Boivinb T, Charmantierc A, Lambrechtsc M, Lavigne C. More daughters in a less favourable world: breeding in intensively-managed orchards affects tertiary sex-ratio in the great tit. Basic Appl Ecol. 2016;17:638-47.

 

Charnov EL. The theory of sex allocation. Princeton: Princeton University Press; 1982.

 

Cichoń M, Sendecka J, Gustafsson L. Male-biased sex ratio among unhatched eggs in great tit Parus major, blue tit P. caeruleus and collared flycatcher Ficedula albicollis. J Avian Biol. 2005;36:386-90.

 

Cordero PJ, Griffith SC, Aparicio JM, Parkin DT. Sexual dimorphism in house sparrow eggs. Behav Ecol Sociobiol. 2000;48:353-7.

 

Daan S, Dijkstra C, Weissing FJ. An evolutionary explanation for seasonal trends in avian sex ratios. Behav Ecol. 1996;7:426-30.

 

Ding Z, Tang S, Zhang J, Chen Y, Hu H. Autumn moulting of the adults of Yellow-bellied Prinia, Prinia flaviventris. Chin J Zool. 2007;42:28-33 (in Chinese).

 

Ding Z, Li K, Tang S, Hu H. Spring moulting and tail changes of two wren warbler species. Chin J Zool. 2015;50:493-8 (in Chinese).

 

Ding Z, Liang J, Pan X, Hu H. Feeding behavior and nestling growth of Yellow-bellied Prinia (Prinia flaviventris). Chin J Zool. 2016;51:969-76 (in Chinese).

 

Ding Z, Liang J, Zhou Z, Feng Y, Hu H. Comparisons of breeding parameters of two Prinia species. Chin J Zool. 2017;52:417-22 (in Chinese).

 

Dietrich-Bischoff V, Schmoll T, Winkel W, Krackow S, Lubjuhn T. Extra-pair paternity, offspring mortality and offspring sex ratio in the socially monogamous coal tit (Parus ater). Behav Ecol Sociobiol. 2006;60:563-71.

 

Dijkstra C, Daan S, Buker JB. Adaptive seasonal variation in the sex ratio of kestrel broods. Funct Ecol. 1990;4:143-7.

 

Ewen JG, Cassey P, Moller AP. Facultative primary sex ratio variation: a lack of evidence in birds? Proc R Soc B. 2004;271:1277-82.

 

Fisher R. The genetical theory of natural selection. London: Oxford University Press; 1930.

 

Frank SA. Sex allocation theory for birds and mammals. Ann Rev Ecol Syst. 1990;21:13-55.

 

Griffiths R, Double MC, Orr K, Dawson RJ. A DNA test to sex most birds. Mol Ecol. 1998;7:1071-5.

 

Grindstaff JL, Buerkle AC, Casto JM, Nolan V, Ketterson ED. Offspring sex ratio is unrelated to male attractiveness in dark-eyed juncos (Junco hyemalis). Behav Ecol Sociobiol. 2001;50:312-6.

 

Gowaty PA. Differential dispersal, local resource competition, and sex ratio variation in birds. Am Nat. 1993;141:263-80.

 

Hasselquist D, Kempenaers B. Parental care and adaptive brood sex ratio manipulation in birds. Philos Trans R Soc B. 2002;357:363-72.

 

Howe HF. Sex-ratio adjustment in the common grackle. Science. 1977;198:744-6.

 

Huang Q, Wang L, Yang C, Liang W. Comparison of nest site selection of Orthotomus sutorius and O. cucullatus. China. J Ecol. 2015;34:2861-5 (in Chinese).

 

Jones KS, Nakagawa S, Sheldon BC. Environmental sensitivity in relation to size and sex in birds: meta-regression analysis. Am Nat. 2009;174:122-33.

 

Kilner R. Primary and secondary sex ratio manipulation by zebra finches. Anim Behav. 1998;56:155-64.

 

Komdeur J, Pen I. Adaptive sex allocation in birds: the complexities of linking theory and practice. Philos Trans R Soc Lond B. 2002;357:373-80.

 

Korpimaki E, May CA, Parkin DT, Wetton JH, Wiehn J. Environmental- and parental condition-related variation in sex ratio of kestrel broods. J Avian Biol. 2000;31:128-34.

 

Korsten P, Lessells CKM, Mateman AC, van der Velde M, Komdeur J. Primary sex ratio adjustment to experimentally reduced male UV attractiveness in blue tits. Behav Ecol. 2006;17:539-46.

 

Lessells CM. Parentally biased favouritism: why should parents specialize in caring for different offspring? Philos Trans R Soc B. 2002;357:381-403.

 

Ležalová R, Tkadlec E, Oborník M, Šimek J, Honza M. Should males come first? The relationship between offspring hatching order and sex in the black-headed gull Larus ridibundus. J Avian Biol. 2005;36:478-83.

 

Liang CF, Liang JY, Liu LF, Mo XL. A report on the exploration of the flora of Longgang. Guihaia. 1985;5:191-209.

 

Mainwaring MC, Lucy D, Hartley IR. Parentally biased favouritism in relation to offspring sex in zebra finches. Behav Ecol Sociobiol. 2011;65:2261-8.

 

Mead PS, Morton ML, Fish BE. Sexual dimorphism in egg size and implications regarding facultative manipulation of sex in mountain white-crowned sparrows. Condor. 1987;89:798-803.

 

Nager RG, Monaghan P, Griffiths R, Houston DC, Dawson R. Experimental demonstration that offspring sex ratio varies with maternal condition. Proc Natl Acad Sci USA. 1999;96:570-3.

 

Oddie KR. Size matters: competition between male and female great tit offspring. J Anim Ecol. 2000;69:903-12.

 

Olsent PD, Cockburn A. Female-biased sex allocation in peregrine falcons and other raptors. Behav Ecol Sociobiol. 2004;28:417-23.

 

Pérez C, Velando A, Domínguez J. Parental food conditions affect sex-specific embryo mortality in the yellow-legged gull (Larus michahellis). J Ornithol. 2006;147:513-9.

 

Pryke SR, Rollins LA. Mothers adjust offspring sex to match the quality of the rearing environment. Proc R Soc B. 2012;279:4051-7.

 
R Development Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. 2011.http://www.R-project.org/.
 

Smallwood PD, Smallwood J. Seasonal shifts in sex ratios of fledgling American kestrels (Falco parverius paulus): the early bird hypothesis. Evol Ecol. 1998;12:839-53.

 

Soma M, Saito DS, Hasegawa T, Okanoya K. Sex-specific maternal effect on egg mass, laying order, and sibling competition in the Bengalese finch (Lonchura striata var. domestica). Behav Ecol Sociobiol. 2007;61:1695-705.

 

Szekely T, Cuthill IC, Yezerinac S, Griffiths R, Kis J. Brood sex ratio in the Kentish plover. Behav Ecol. 2004;15:58-62.

 

Svenson M, Rintamäki PT, Birkhead TR, Griffith SC, Lundberg A. Impaired hatching success and male-biased embryo mortality in Tree Sparrows. J Ornithol. 2007;148:117-22.

 

Suorsa P, Helle H, Huhta E, Jäntti A, Nikula A, Hakkarainen H. Forest fragmentation is associated with primary brood sex ratio in the treecreeper (Certhia familiaris). Proc R Soc B. 2003;270:2215-22.

 

Taff CC, Freeman-Gallant CR, Dunn PO, Whittingham LA. Relationship between brood sex ratio and male ornaments depends on male age in a warbler. Anim Behav. 2011;81:619-25.

 

Velando A. Experimental manipulation of maternal effort produces differential effects in sons and daughters: implications for adaptive sex ratios in the blue-footed booby. Behav Ecol. 2002;13:443-9.

 

Wang L, Liang W, Yang C, Cheng S, Hsu Y, Lu X. Egg rejection and clutch phenotype variation in the plain prinia Prinia inornata. J Avian Biol. 2016;47:788-94.

 

West SA, Sheldon BC. Constraints in the evolution of sex ratio adjustment. Science. 2002;295:1685-8.

 

Weimerskirch H, Barbraud C, Lys P. Sex differences in parental investment and chick growth in wandering albatrosses: fitness consequences. Ecology. 2000;81:309-18.

 

Whittingham LA, Dunn PO. Effects of extra-pair and within-pair reproductive success on the opportunity for selection in birds. Behav Ecol. 2005;16:138-44.

 

Yamaguchi N, Kawano KK, Eguchi K, Yahara T. Facultative sex ratio adjustment in response to male tarsus length in the Varied Tit Parus varius. Ibis. 2004;146:108-13.

 

Yang C, Wang L, Hsu YC, Antonov A, Moksnes A, Røskaft E, Liang W, Stokke BG. UV reflectance as a cue in egg discrimination in two prinia species exploited differently by brood parasites in Taiwan. Ibis. 2013;155:571-5.

 

Yang C, Wang L, Cheng SJ, Hsu YC, Liang W, Møller AP. Nest defenses and egg recognition of Yellow-bellied Prinia against cuckoo parasitism. Naturwissenschaften. 2014;101:727-34.

 

Zhao Z. A handbook of the birds of China: Passerines. Changchu: Jilin Science and Technology Press; 2001 (in Chinese).

 

Zheng G. A checklist on the classification and distribution of the birds of China. Beijing: Science Press; 2011 (in Chinese).

Avian Research
Article number: 15
Cite this article:
Ding Z, Ji F, Huang Q, et al. Brood sex ratio in the Yellow-bellied Prinia (Prinia flaviventris). Avian Research, 2017, 8(1): 15. https://doi.org/10.1186/s40657-017-0074-5

583

Views

17

Downloads

3

Crossref

N/A

Web of Science

3

Scopus

0

CSCD

Altmetrics

Received: 31 January 2017
Accepted: 22 June 2017
Published: 30 June 2017
© The Author(s) 2017.

This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Return