Schulte-hostedde Etal Morphology

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calliper, accuracy 0.01 mm; Schulte-Hostedde et al. 2005). All variables. mental differences in Hoopoe preen gland morphology and secretions. Evidence for a.

Our results show that low variation in sperm size is strongly related to high sperm velocity and normal sperm morphology, which in turn are good predictors of male fertility in this species.

27 Oct 2016. size dimorphism (Schulte-Hostedde et al. 2002; Edelman and. are larger than males in all morphological measurements. (Levenson 1990).

Conversely, it is also possible to learn the graph structure, in our case the trophic net-. Reynolds et al., 2009; Schulte-Hostedde et al., 2005). Alternative, but.

Our results show that low variation in sperm size is strongly related to high sperm velocity and normal sperm morphology, which in turn are good predictors of male fertility in this species.

of mating success and broodstock development (Gage et al., 2004. Burness, G. ; Schulte-Hostedde, A. I.; Casselman, S. J.; Moyes, C. D.;. Montgomerie, R.

Our results highlight the importance of understanding how interactions between sexual selection pressures, and between behavior and morphology, function to influence male reproductive success. We used.

14 Jan 2019. 2015; Seddon et al., 2013; Simmons & Fitzpatrick, 2016). Sperm is. with body condition (Bonanno & Schulte- Hostedde, 2009; Kahrl. & Cox.

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Typical of male genital morphology generally, the mammalian baculum or. 57. 2004; Miller and Nagorsen 2008; Ramm et al. 2010; Schulte-Hostedde et al.

including previously unpublished genetic data and analyses that indicate that the many instances of mitochondrial introgression we have identified illustrate a gradual attenuation of gene flow with.

An association between male fertility and certain RNAs has been shown in humans but the mechanisms involved are unknown (Jodar et al. 2012). The hypotheses outlined above for the evolution of genetic.

favored by sexual and fecundity selection (Schulte-Hostedde et al. 2002). Here, we ask. Consequently, the age structure of the breeding population dif-.

In addition, human-mediated transport of founding individuals over long distances results in large geographical ranges for these species and colonisation of new areas, which would otherwise be.

Fairbairn 2000; Badyaev and Martin 2000; Schulte-Hostedde et al. 2002). Long- term. sexual differences in trophic morphology (an indicator of ecological.

26 Jun 2013. By providing the first evidence linking baculum morphology to male reproductive success, Tasikas DE, Fairn ER, Laurence S, Schulte-Hostedde AI: Baculum variation and. Stockley, P., Ramm, S.A., Sherborne, A.L. et al.

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In addition, human-mediated transport of founding individuals over long distances results in large geographical ranges for these species and colonisation of new areas, which would otherwise be.

Our results highlight the importance of understanding how interactions between sexual selection pressures, and between behavior and morphology, function to influence male reproductive success. We used.