John Hunt

John Hunt

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John Hunt

School of Science, Western Sydney University, Richmond, Australia

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2004 in Nature
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JHJohn Hunt
John Hunt
RBRobert Brooks
Robert Brooks
MJMichael D. Jennions
Michael D. Jennions
MSMichael J. Smith
Michael J. Smith
CBCaroline L. Bentsen
Caroline L. Bentsen
LBLuc F. Bussière
Luc F. Bussière

18 December 2008 in Journal of Evolutionary Biology
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JHJohn Hunt
John Hunt
CBCasper Johannes Breuker
Casper Johannes Breuker
JSJennifer A. Sadowski
Jennifer A. Sadowski
AMAllen J. Moore
Allen J. Moore
Empirical studies of sexual selection typically focus on one of the two mechanisms of sexual selection without integrating these into a description of total sexual selection, or study total sexual selection without quantifying the contributions of all of the mechanisms of sexual selection. However, this can provide an incomplete or misleading view of how sexually selected traits evolve if the mechanisms of sexual selection are opposing or differ in form. Here, we take a two‐fold approach to advocate a direction for future studies of sexual selection. We first show how a quantitative partitioning and examination of sexual selection mechanisms can inform by identifying illustrative studies that describe both male–male competition and female mate choice acting on the same trait. In our sample, the most common trait where this occurred was body size, and selection was typically linear. We found that male–male competition and female mate choice can be reinforcing or opposing, although the former is most common in the literature. The mechanisms of sexual selection can occur simultaneously or sequentially, and we found they were more likely to be opposing when the mechanisms operated sequentially. The degree and timing that these mechanisms interact have important implications for the operation of sexual selection and needs to be considered in designing studies. Our examples highlight where empirical data are needed. We especially lack standardized measures of the form and strength of selection imposed by each mechanism of sexual selection and how they combine to determine total sexual selection. Secondly, using quantitative genetic principles, we outline how the selection imposed by individual mechanisms can be measured and combined to estimate the total strength and form of sexual selection. We discuss the evolutionary consequences of combining the mechanisms of sexual selection and interpreting total sexual selection. We suggest how this approach may result in empirical progress in the field of sexual selection.

1 July 2005 in The American Naturalist
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JHJohn Hunt
John Hunt
RBRobert Brooks
Robert Brooks
MJMichael D. Jennions
Michael D. Jennions
The acquisition of resources is an important determinant of patterns of variation in and covariation among traits that are costly to produce and are dependent on condition for their expression. However, the extent to which variation in female mate choice behavior is condition dependent, and how this is related to other life‐history traits, remains largely unknown. We manipulated the acquisition of dietary protein in the black field cricket, Teleogryllus commodus, and measured the effects of this on several important life‐history traits and on female mate choice behavior. Females reared on a high‐protein diet developed faster, were heavier at eclosion, and lived longer than females reared on a low‐protein diet. Two lines of evidence suggest that female mate choice behavior in T. commodus is condition dependent. First, females reared on the high‐protein diet were more sexually responsive and expressed stronger linear and quadratic preference functions for call rate and dominant frequency, respectively. Second, within treatments, females that developed faster were lighter, generally less sexually responsive, and, in the high‐protein‐diet treatment, expressed weaker preferences than slower‐developing females. Collectively, our findings suggest an important role for resource acquisition in generating variation in mate choice behavior.

23 March 2015 in Aging Cell
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KJKim Jensen
Kim Jensen
CMColin McClure
Colin McClure
NPNicholas K. Priest
Nicholas K. Priest
JHJohn Hunt
John Hunt
Modest dietary restriction extends lifespan (LS) in a diverse range of taxa and typically has a larger effect in females than males. Traditionally, this has been attributed to a stronger trade-off between LS and reproduction in females than in males that is mediated by the intake of calories. Recent studies, however, suggest that it is the intake of specific nutrients that extends LS and mediates this trade-off. Here, we used the geometric framework (GF) to examine the sex-specific effects of protein (P) and carbohydrate (C) intake on LS and reproduction in Drosophila melanogaster. We found that LS was maximized at a high intake of C and a low intake of P in both sexes, whereas nutrient intake had divergent effects on reproduction. Male offspring production rate and LS were maximized at the same intake of nutrients, whereas female egg production rate was maximized at a high intake of diets with a P:C ratio of 1:2. This resulted in larger differences in nutrient-dependent optima for LS and reproduction in females than in males, as well as an optimal intake of nutrients for lifetime reproduction that differed between the sexes. Under dietary choice, the sexes followed similar feeding trajectories regulated around a P:C ratio of 1:4. Consequently, neither sex reached their nutritional optimum for lifetime reproduction, suggesting intralocus sexual conflict over nutrient optimization. Our study shows clear sex differences in the nutritional requirements of reproduction in D. melanogaster and joins the growing list of studies challenging the role of caloric restriction in extending LS.

11 January 2012 in Proceedings Of The Royal Society B-Biological Sciences
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KJKim Jensen
Kim Jensen
DMDavid Mayntz
David Mayntz
STSøren Toft
Søren Toft
FCFiona J. Clissold
Fiona J. Clissold
JHJohn Hunt
John Hunt
SSStephen J. Simpson
Stephen J. Simpson
Evolutionary theory predicts that animals should forage to maximize their fitness, which in predators is traditionally assumed equivalent to maximizing energy intake rather than balancing the intake of specific nutrients. We restricted female predatory ground beetles ( Anchomenus dorsalis ) to one of a range of diets varying in lipid and protein content, and showed that total egg production peaked at a target intake of both nutrients. Other beetles given a choice to feed from two diets differing only in protein and lipid composition selectively ingested nutrient combinations at this target intake. When restricted to nutritionally imbalanced diets, beetles balanced the over- and under-ingestion of lipid and protein around a nutrient composition that maximized egg production under those constrained circumstances. Selective foraging for specific nutrients in this predator thus maximizes its reproductive performance. Our findings have implications for predator foraging behaviour and in the structuring of ecological communities.

3 November 2015 in Biological Reviews
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DPDaniel Pincheira-Donoso
Daniel Pincheira-Donoso
JHJohn Hunt
John Hunt
Fitness results from an optimal balance between survival, mating success and fecundity. The interactions between these three components of fitness vary depending on the selective context, from positive covariation between them, to antagonistic pleiotropic relationships when fitness increases in one reduce the fitness of others. Therefore, elucidating the routes through which selection shapes life history and phenotypic adaptations via these fitness components is of primary significance to understanding ecological and evolutionary dynamics. However, while the fitness components mediated by natural (survival) and sexual (mating success) selection have been debated extensively from most possible perspectives, fecundity selection remains considerably less studied. Here, we review the theoretical basis, evidence and implications of fecundity selection as a driver of sex‐specific adaptive evolution. Based on accumulating literature on the life‐history, phenotypic and ecological aspects of fecundity, we (i) suggest a re‐arrangement of the concepts of fecundity, whereby we coin the term ‘transient fecundity’ to refer to brood size per reproductive episode, while ‘annual’ and ‘lifetime fecundity’ should not be used interchangeably with ‘transient fecundity’ as they represent different life‐history parameters; (ii) provide a generalized re‐definition of the concept of fecundity selection as a mechanism that encompasses any traits that influence fecundity in any direction (from high to low) and in either sex; (iii) review the (macro)ecological basis of fecundity selection (e.g. ecological pressures that influence predictable spatial variation in fecundity); (iv) suggest that most ecological theories of fecundity selection should be tested in organisms other than birds; (v) argue that the longstanding fecundity selection hypothesis of female‐biased sexual size dimorphism (SSD) has gained inconsistent support, that strong fecundity selection does not necessarily drive female‐biased SSD, and that this form of SSD can be driven by other selective pressures; and (vi) discuss cases in which fecundity selection operates on males. This conceptual analysis of the theory of fecundity selection promises to help illuminate one of the central components of fitness and its contribution to adaptive evolution.