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dc.contributor.authorLangen, E
dc.contributor.authorvon Engelhardt, NB
dc.contributor.authorGoerlich-Jansson, V
dc.date.accessioned2018-04-13T07:22:44Z
dc.date.issued2018-07-01
dc.identifier.issn0016-6480
dc.identifier.issn1095-6840
dc.identifier.urihttp://hdl.handle.net/10026.1/11269
dc.description.abstract

The social environment of reproducing females can cause physiological changes, with consequences for reproductive investment and offspring development. These prenatal maternal effects are often found to be sex-specific and may have evolved as adaptations, maximizing fitness of male and female offspring for their future environment. Female hormone levels during reproduction are considered a potential mechanism regulating sex allocation in vertebrates: high maternal androgens have repeatedly been linked to increased investment in sons, whereas high glucocorticoid levels are usually related to increased investment in daughters. However, results are not consistent across studies and therefore still inconclusive. In Japanese quail (Coturnix japonica), we previously found that pair-housed females had higher plasma androgen levels and tended to have higher plasma corticosterone levels than group-housed females. In the current study we investigate whether these differences in maternal social environment and physiology affect offspring sex allocation and physiology. Counter to our expectations, we find no effects of the maternal social environment on offspring sex ratio, sex-specific mortality, growth, circulating androgen or corticosterone levels. Also, maternal corticosterone or androgen levels do not correlate with offspring sex ratio or mortality. The social environment during reproduction therefore does not necessarily modify sex allocation and offspring physiology, even if it causes differences in maternal physiology. We propose that maternal effects of the social environment strongly depend upon the type of social stimuli and the timing of changes in the social environment and hormones with respect to the reproductive cycle and meiosis.

dc.format.extent12-20
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherElsevier
dc.subjectFetal programming
dc.subjectSteroids
dc.subjectDevelopment
dc.subjectMortality
dc.subjectStress response
dc.subjectSex allocation
dc.titleNo evidence for sex-specific effects of the maternal social environment on offspring development in Japanese quail (Coturnix japonica)
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/29684400
plymouth.volume263
plymouth.publication-statusPublished
plymouth.journalGeneral and Comparative Endocrinology
dc.identifier.doi10.1016/j.ygcen.2018.04.015
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Biological and Marine Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA04 Psychology, Psychiatry and Neuroscience
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2018-04-12
dc.rights.embargodate2019-4-22
dc.identifier.eissn1095-6840
dc.rights.embargoperiodNo embargo
rioxxterms.funderVolkswagen Foundation
rioxxterms.identifier.projectEvolution of transgenerational effects: function & genetics of epigenetics.
rioxxterms.versionofrecord10.1016/j.ygcen.2018.04.015
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2018-07-01
rioxxterms.typeJournal Article/Review
plymouth.funderEvolution of transgenerational effects: function & genetics of epigenetics.::Volkswagen Foundation


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