2020
DOI: 10.1007/s00114-020-01674-1
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Testosterone and the dark ventral patch of male red deer: the role of the social environment

Abstract: The expression of male sexual traits, which is stimulated by testosterone, entails significant costs for individuals. Consequently, natural selection is expected to favour the modulation of sexual trait development according to the balance between its costs and benefits. The proportion of rivals in a population may affect this balance by increasing or decreasing the reproductive benefits associated with the development of sex traits. Here, we explore the relationship between testosterone level and sex-trait si… Show more

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Cited by 11 publications
(11 citation statements)
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“…Males with larger antlers in HC environment showed low testosterone levels in agreement with the expectation, while variation in antler size and testosterone were higher among LC males. Results for the dark ventral patch in Iberian red deer populations showed a positive relationship between this trait and testosterone, but only in HC populations (de la Peña et al 61 ) Both results suggest that the relationship between testosterone and sex traits may be weaker when sexual competition is lower, but further research is needed.…”
Section: Random Effectsmentioning
confidence: 96%
“…Males with larger antlers in HC environment showed low testosterone levels in agreement with the expectation, while variation in antler size and testosterone were higher among LC males. Results for the dark ventral patch in Iberian red deer populations showed a positive relationship between this trait and testosterone, but only in HC populations (de la Peña et al 61 ) Both results suggest that the relationship between testosterone and sex traits may be weaker when sexual competition is lower, but further research is needed.…”
Section: Random Effectsmentioning
confidence: 96%
“…The four measurements of parasites defined in this study were: (1) Prevalence, the number of hosts infected with one or more individuals of a particular parasitic species (or taxonomic group), divided by the number of hosts examined for that parasitic species ( Bush et al, 1997 ). (2) Parasite burden was estimated as the number of a parasitic form (oocysts, eggs or larvae) in a single faecal sample ( Bush et al, 1997 ; De la Peña et al, 2020a ). In this study the parasite burden was assessed by calculating the faecal oocyst or egg counts.…”
Section: Methodsmentioning
confidence: 99%
“…Parasite dynamics can be affected by abiotic factors (such as season and climatic conditions); for example, precipitation caused significant changes in the gastrointestinal parasites of eastern chimpanzees ( Gillespie et al, 2010 ) and temperature had a significant impact on the transmission of parasites in the gastrointestinal tracts of Arctic ungulates ( Kafle et al, 2018 ). Alpine chamois and red deer parasite burden was affected by various biotic factors, including reproduction and immune status ( Corlatti et al, 2012 ; De la Peña et al, 2020a ). The host often faces a life history trade-off between reproduction and immunity ( Corlatti et al, 2012 ; De la Peña et al, 2020a ).…”
Section: Introductionmentioning
confidence: 99%
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“…Regarding the frequency histogram of the dark ventral patch size (see Fig 1 ), we checked for unimodality or multimodality, estimating the distribution underlying this trait by Hartigans’ dip test using the package diptest [ 41 ]. In previous assessments, the frequency histogram of the size of the dark ventral patch showed a data gap in values between 40 and 50 cm [ 42 , 43 ]. Thus, we maintained here the cut point used in previous analyses that followed the distribution gap appearing in previous data sets, and defined two groups: low trait expression males, those that had between 0 and 50 cm of darkness area in their bellies, and those that had more than 50 cm, even the whole ventral area dark, high trait expression males.…”
Section: Methodsmentioning
confidence: 99%