Russell Bonduriansky

Bio: Russell Bonduriansky is an academic researcher from University of New South Wales. The author has contributed to research in topics: Sexual selection & Sexual conflict. The author has an hindex of 39, co-authored 107 publications receiving 8014 citations. Previous affiliations of Russell Bonduriansky include University of Toronto & University of Guelph.

The evolution of male mate choice in insects: a synthesis of ideas and evidence.

Abstract: Mate choice by males has been recognized at least since Darwin's time, but its phylogenetic distribution and effect on the evolution of female phenotypes remain poorly known. Moreover, the relative importance of factors thought to underlie the evolution of male mate choice (especially parental investment and mate quality variance) is still unresolved. Here I synthesize the empirical evidence and theory pertaining to the evolution of male mate choice and sex role reversal in insects, and examine the potential for male mating preferences to generate sexual selection on female phenotypes. Although male mate choice has received relatively little empirical study, the available evidence suggests that it is widespread among insects (and other animals). In addition to 'precopulatory' male mate choice, some insects exhibit 'cryptic' male mate choice, varying the amount of resources allocated to mating on the basis of female mate quality. As predicted by theory, the most commonly observed male mating preferences are those that tend to maximize a male's expected fertilization success from each mating. Such preferences tend to favour female phenotypes associated with high fecundity or reduced sperm competition intensity. Among insect species there is wide variation in mechanisms used by males to assess female mate quality, some of which (e.g. probing, antennating or repeatedly mounting the female) may be difficult to distinguish from copulatory courtship. According to theory, selection for male choosiness is an increasing function of mate quality variance and those reproductive costs that reduce, with each mating, the number of subsequent matings that a male can perform ('mating investment') Conversely, choosiness is constrained by the costs of mate search and assessment, in combination with the accuracy of assessment of potential mates and of the distribution of mate qualities. Stronger selection for male choosiness may also be expected in systems where female fitness increases with each copulation than in systems where female fitness peaks at a small number of matings. This theoretical framework is consistent with most of the empirical evidence. Furthermore, a variety of observed male mating preferences have the potential to exert sexual selection on female phenotypes. However, because male insects typically choose females based on phenotypic indicators of fecundity such as body size, and these are usually amenable to direct visual or tactile assessment, male mate choice often tends to reinforce stronger vectors of fecundity or viability selection, and seldom results in the evolution of female display traits. Research on orthopterans has shown that complete sex role reversal (i.e. males choosy, females competitive) can occur when male parental investment limits female fecundity and reduces the potential rate of reproduction of males sufficiently to produce a female-biased operational sex ratio. By contrast, many systems exhibiting partial sex role reversal (i.e. males choosy and competitive) are not associated with elevated levels of male parental investment, reduced male reproductive rates, or reduced male bias in the operational sex ratio. Instead, large female mate quality variance resulting from factors such as strong last-male sperm precedence or large variance in female fecundity may select for both male choosiness and competitiveness in such systems. Thus, partial and complete sex role reversal do not merely represent different points along a continuum of increasing male parental investment, but may evolve via different evolutionary pathways.

Intralocus sexual conflict.

Abstract: Intralocus sexual conflict occurs when selection on a shared trait in one sex displaces the other sex from its phenotypic optimum. It arises because many shared traits have a common genetic basis but undergo contrasting selection in the sexes. A recent surge of interest in this evolutionary tug of war has yielded evidence of such conflicts in laboratory and natural populations. Here we highlight outstanding questions about the causes and consequences of intralocus sexual conflict at the genomic level, and its long-term implications for sexual coevolution. Whereas recent thinking has focussed on the role of intralocus sexual conflict as a brake on sexual coevolution, we urge a broader appraisal that also takes account of its potential to drive adaptive evolution and speciation.

Eliminating autocorrelation reduces biological relevance of home range estimates

Abstract: 1. Destructive subsampling or restrictive sampling are often standard procedures to obtain independence of spatial observations in home range analyses. We examined whether home range estimators based upon kernel densities require serial independence of observations, by using a Monte Carlo simulation, antler flies and snapping turtles as models. 2. Home range size, time partitioning and total straight line distances travelled were tested to determine if subsampling improved kernel performance and estimation of home range parameters. 3. The accuracy and precision of home range estimates from the simulated data set improved at shorter time intervals despite the increase in autocorrelation among the observations. 4. Subsampling did not reduce autocorrelation among locational observations of snapping turtles or antler flies, and home range size, time partitioning and total distance travelled were better represented by autocorrelated observations. 5. We found that kernel densities do not require serial independence of observations when estimating home range, and we recommend that researchers maximize the number of observations using constant time intervals to increase the accuracy and precision of their estimates.

Nongenetic Inheritance and Its Evolutionary Implications

Abstract: Modern evolutionary biology is founded on the Mendelian-genetic model of inheritance, but it is now clear that this model is incomplete. Empirical evidence shows that environment (encompassing all external influences on the genome) can impose transgenerational effects and generate heritable variation for a broad array of traits in animals, plants, and other organisms. Such effects can be mediated by the transmission of epigenetic, cytoplasmic, somatic, nutritional, environmental, and behavioral variation. Building on the work of many authors, we outline a general framework for conceptualizing nongenetic inheritance and its evolutionary implications. This framework shows that, by decoupling phenotypic change from the genotype, nongenetic inheritance can circumvent the limitations of genetic inheritance and thereby influence population dynamics and alter the fitness landscape. The weight of theory and empirical evidence indicates that nongenetic inheritance is a potent factor in evolution that can engender ...

Sexual selection, sexual conflict and the evolution of ageing and life span

Abstract: Summary 1Classic evolutionary models interpret ageing as a cost of reproduction, but evolutionary research has thus far largely neglected the conceptual links between the evolution of ageing and a key mode of selection on male and female reproductive strategies – sexual selection and sexual conflict. 2We synthesize ideas and evidence linking sex and ageing, and make the case that a focus on this fascinating problem will ultimately lead to a more complete understanding of both the evolution of ageing and the evolution of sexual strategies. 3The primary and secondary differentiation of male and female reproductive strategies is expected to produce sex-specific optima for traits that affect longevity and ageing rate, often favouring a ‘live fast, die young’ strategy in males, relative to females, although numerous exceptions to this pattern are observed and sex-differences in ageing rate, in particular, remain poorly understood. 4Conversely, environmental factors that influence life expectancy or ageing rate can thereby determine the magnitude or even sign of sexual selection. 5Sexual conflict is expected to displace the sexes from their sex-specific life-history optima through sexually antagonistic interactions, as well as sex-specific selection on loci expressed in both sexes. 6Despite the availability of interesting and testable hypotheses linking sexual selection and ageing, relevant empirical studies are remarkably sparse, and the complex relation between sex, mortality rate and ageing remains poorly understood.

Human biochemical genetics

Abstract: So far in this course we have dealt entirely with the evolution of characters that are controlled by simple Mendelian inheritance at a single locus. There are notes on the course website about gametic disequilibrium and how allele frequencies change at two loci simultaneously, but we didn’t discuss them. In every example we’ve considered we’ve imagined that we could understand something about evolution by examining the evolution of a single gene. That’s the domain of classical population genetics. For the next few weeks we’re going to be exploring a field that’s actually older than classical population genetics, although the approach we’ll be taking to it involves the use of population genetic machinery. If you know a little about the history of evolutionary biology, you may know that after the rediscovery of Mendel’s work in 1900 there was a heated debate between the “biometricians” (e.g., Galton and Pearson) and the “Mendelians” (e.g., de Vries, Correns, Bateson, and Morgan). Biometricians asserted that the really important variation in evolution didn’t follow Mendelian rules. Height, weight, skin color, and similar traits seemed to

The descent of man and selection in relation to sex

Abstract: ION, GENERAL CONCEPTIONS, SELF-CONSCIOUSNESS, MENTAL INDIVIDUALITY. It would be very difficult for any one with even much more knowledge than I possess, to determine how far animals exhibit any traces of these high mental powers. This difficulty arises from the impossibility of judging what passes through the mind of an animal; and again, the fact that writers differ to a great extent in the meaning which they attribute to the above terms, causes a further difficulty. If one may judge from various articles which have been published lately, the greatest stress seems to be laid on the supposed entire absence in animals of the power of abstraction, or of forming general concepts. But when a dog sees another dog at a distance, it is often clear that he perceives that it is a dog in the abstract; for when he gets nearer his whole manner suddenly changes, if the other dog be a friend. A recent writer remarks, that in all such cases it is a pure assumption to assert that the mental act is not essentially of the same nature in the animal as in man. If either refers what he perceives with his senses to a mental concept, then so do both. (44. Mr. Hookham, in a letter to Prof. Max Muller, in the 'Birmingham News,' May, 1873.) When I say to my terrier, in an eager voice (and I have made the trial many times), "Hi, hi, where is it?" she at once takes it as a sign that something is to be hunted, and generally first looks quickly all around, and then rushes into the nearest thicket, to scent for any game, but finding nothing, she looks up into any neighbouring tree for a squirrel. Now do not these actions clearly shew that she had in her mind a general idea or concept that some animal is to be discovered and hunted? It may be freely admitted that no animal is self-conscious, if by this term it is implied, that he reflects on such points, as whence he comes or whither he will go, or what is life and death, and so forth. But how can we feel sure that an old dog with an excellent memory and some power of imagination, as shewn by his dreams, never reflects on his past pleasures or pains in the chase? And this would be a form of self-consciousness. On the other hand, as Buchner (45. 'Conferences sur la Theorie Darwinienne,' French translat. 1869, p. 132.) has remarked, how little can the hardworked wife of a degraded Australian savage, who uses very few abstract words, and cannot count above four, exert her self-consciousness, or reflect on the nature of her own existence. It is generally admitted, that the higher animals possess memory, attention, association, and even some imagination and reason. If these powers, which differ much in different animals, are capable of improvement, there seems no great improbability in more complex faculties, such as the higher forms of abstraction, and selfconsciousness, etc., having been evolved through the development and combination of the simpler ones. It has been urged against the views here maintained that it is impossible to say at what point in the ascending scale animals become capable of abstraction, etc.; but who can say at what age this occurs in our young children? We see at least that such powers

Spatial Analysis A Guide for Ecologists

Abstract: Preface 1. Spatial concepts and notions 2. Ecological and spatial processes 3. Points, lines and graphs 4. Spatial analysis of complete point location data 5. Contiguous units analysis 6. Spatial analysis of sample data 7. Spatial relationship and multiscale analysis 8. Spatial autocorrelation and inferential tests 9. Spatial partitioning: spatial clusters and boundary detection 10. Spatial diversity analysis 11. Spatio-temporal analysis 12. Closing comments and future directions References Index.