Life history biology sits on the interface between genetics and ecology, and both have made important theoretical and empirical contributions to our understanding. However, the connections between the disciplines have not always been as close as they might have been and this book takes some useful steps towards remedying this. It gives an excellent review of life history theory, and integrates this well with results from the empirical literature. After an 11-page introduction, Roff sets out ‘a framework for analysis’ in which he covers the necessary elements of quantitative and population genetics. This includes clear definitions of fitness in a range of circumstances, from density independent populations in constant environments through to the more complex situations of density and frequency dependence and environments that are spatially or temporally stochastic. Trade-offs are then examined, including a valuable analysis of potential pitfalls in studying them and ways that these can be avoided. The author then deals in turn with evolution in constant environments; stochastic environments and ‘predictable environments’. The last of these covers situations where there is environmental variation, but at least some information is available to allow individuals to make an adaptive response. The final chapter identifies 20 topics for future study. Some will find the book too dominated by theory. Others (but probably not readers of Heredity!) will find it contains too much genetics. But Roff does an excellent job of making the theory accessible, covering the essential issues and pointing to original sources for the details. Theory is related to a significant number of empirical studies, although there is room for another book reviewing the empirical literature on life histories in detail, and Roff’s book would provide a robust skeleton on which to hang this. To make my own assessment, I examined in detail Roff’s discussion of the question of fitness measures for density dependent populations in stochastic environments – an area in which I have been involved. I could not fault him – all the key references were there and the issues were made very clear without the more esoteric mathematics. I also examined some areas that I was less familiar with, and again the text was clear and easy to read. My only real criticism of the book would be that its very long chapters (more than 130 pages in one case) makes it difficult to find things. It would have been simple to address this by including the section headings on the contents pages. A minor personal quibble would be that the book usually expresses problems in terms of the intrinsic rate of increase, r, and the characteristic (Lotka) equation. A matrix formulation is often more tractable and is easier to generalise to density dependent populations and stochastic environments, so expanding on the relationship between the two would have been useful. But overall this is an excellent book. It brings together the key theory in a single place. It gives an invaluable route into the literature, with a bibliography of 1600 or so items. These features, and its identification of topics that need further study should make an important contribution to moving the field forward.

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Life History Evolution

Preface 1 Bounded and Rational 2 Fast and Frugal heuristics 3 Rules of Thumb in Animals and Humans 4 I Think, Therefore I Err 5 Striking a Blow for Sanity in Theories of Rationality 6 Out of the Frying Pan Into the Fire 7 What's in a Sample? A Manual for Building Cognitive Theories 8 "A 30% Chance of Rain Tomorrow" 9 Simple Tools for Understanding Risks: From Innumeracy to Insight 10 The Evolution of Statistical Thinking 11 Mindless Statistics 12 Children Can Solve Bayesian Problems 13 In the year 2054" Innumeracy Defeated References Subject Index Name index

Rationality for Mortals: How People Cope with Uncertainty

Every plant is a member of a complex insect community that consists of tens to hundreds of species that belong to different trophic levels. The dynamics of this community are critically influenced by the plant, which mediates interactions between community members that can occur on the plant simultaneously or at different times. Herbivory results in changes in the plant's morphological or chemical phenotype that affect interactions with subsequently arriving herbivores. Changes in the plant's phenotype are mediated by molecular processes such as phytohormonal signaling networks and transcriptomic rearrangements that are initiated by oral secretions of the herbivore. Processes at different levels of biological complexity occur at timescales ranging from minutes to years. In this review, we address plant-mediated interactions with multiple species of the associated insect community and their effects on community dynamics, and link these to the mechanistic effects that multiple attacks have on plant phenotypes.

Plant Interactions with Multiple Insect Herbivores: From Community to Genes

https://pure.mpg.de/pubman/item/item_2101028_4/component/file_2101027/JH_Simple_2005.pdf

Simple heuristics and rules of thumb: Where psychologists and behavioural biologists might meet

Measurement of Diversity of Human Field Pattern

We compared the expression profiles of jasmonic acid (JA)-inducible genes (Pin2 and LapA1) and salicylic acid (SA)-inducible genes (PRb-1b and GluB) in the tomato (Solanum lycopersicum cv. Micro-Tom) against herbivores using differing feeding modes: the leaf-chewing larvae of the insects Spodoptera litura and S. exigua; the western flower thrips (Frankliniella occidentalis) and the two-spotted spider mite (Tetranychus urticae) as cell-content feeders; and the leaf miner fly (Liriomyza sativae). Feeding by larvae of both S. litura and S. exigua chiefly activated JA-inducible genes, similar to the response to wound stimuli. Feeding by the thrips F. occidentalis also activated JA-inducible genes, as previously reported in Arabidopsis. Feeding by the spider mite T. urticae activated a JA-inducible LapA1 gene but did not activate a JA-inducible Pin2 gene and additionally activated SA-inducible genes, which were accompanied by the accumulation of SA. This may be a strain that represses induction of the JA signaling pathway. One day after oviposition by the leaf miner fly, L. sativae, JA-inducible genes were activated. However, after the L. sativae larvae hatched and began eating within the leaf tissues, JA-inducible gene expression decreased and SA-inducible gene expression increased. Activation of SA-inducible genes (PRb-1b and GluB) by L. sativae larval feeding seems to suppress JA-mediated plant defense but appears to be unrelated to SA accumulation.

https://link.springer.com/content/pdf/10.1007%2Fs11829-015-9412-x.pdf

Different expression profiles of jasmonic acid and salicylic acid inducible genes in the tomato plant against herbivores with various feeding modes

Waste management behavior is essential to achieve nest sanitation that is highly inferential on the evolution of group living because nest waste is an inevitable cost. However, how group living animals dispose of waste has not attracted much attention. Schizotetranychus miscanthi Saito is a social spider mite infesting a perennial grass (Miscanthus sinensis Anderss), in which all nest members tend to defecate at specific sites. We investigated the mechanisms by which the individuals select the site of defecation. The results show that nest members defecate at only one site inside the nest, and that waste management is maintained by two simple rules. First, mites defecate near the nest entrances if no volatile chemical cues are available, and secondly, when chemical cues are available from feces deposited previously, they defecate at this site. We discuss the adaptive significance of these mechanisms, as well as their role in the evolution of sociality in mites.

Rules for Nest Sanitation in a Social Spider Mite, Schizotetranychus miscanthi Saito (Acari: Tetranychidae)

When phylogenetically close, two competing species may reproductively interfere, and thereby affect their population dynamics. We tested for reproductive interference (RI) between two congeneric haplo-diploid spider mites, Tetranychus evansi and Tetranychus urticae, by investigating their interspecific mating and their population dynamics when they competed on the same plants. They are both pests of tomato, but differ in the host plant defences that they suppress or induce. To reduce the effect of plant-mediated interaction, we used a mutant tomato plant lacking jasmonate-mediated anti-herbivore defences in the competition experiment. In addition, to manipulate the effect of RI, we introduced founder females already mated with conspecific males in mild RI treatments or founder, virgin females in strong RI treatments (in either case together with heterospecific and conspecific males). As females show first-male sperm precedence, RI should occur especially in the founder generation under strong RI treatments. We found that T. urticae outcompeted T. evansi in mild, but not in strong RI treatments. Thus, T. evansi interfered reproductively with T. urticae. This result was supported by crossing experiments showing frequent interspecific copulations, strong postmating reproductive isolation and a preference of T. evansi males to mate with T. urticae (instead of conspecific) females, whereas T. urticae males preferred conspecific females. We conclude that interspecific mating comes at a cost due to asymmetric mate preferences of males. Because RI by T. evansi can improve its competitiveness to T. urticae, we propose that RI partly explains why T. evansi became invasive in Europe where T. urticae is endemic.

/pdf/testing-for-reproductive-interference-in-the-population-3yxjcbd1ki.pdf

Testing for reproductive interference in the population dynamics of two congeneric species of herbivorous mites

Post-copulatory associations between males and females have been found in a variety of insects and are often described as mate guarding. Males of the West Indian sweetpotato weevil Euscepes postfasciatus (Fairmaire) mount the female's back after copulation. Two hypotheses have been advanced to explain this behavior: mate guarding to prevent future copulations by rivals (hypothesis 1), and mate guarding to gain additional copulations (hypothesis 2). We conducted three experiments to test predictions from these hypotheses. Our results disproved hypothesis 1 because the duration of the post-copulatory association was very brief in comparison with the length of the refractory phase all females showed after copulation. When we prevented females from resisting copulations during the post-copulatory mounted phase males copulated again, while under normal conditions, a second copulation was never observed. This result may indicate the presence of a sexual conflict over mating. However, we propose an alternative interpretation of the result, namely that after mating, males test whether the copulation has successfully reduced female receptivity by attempting to remate. If females resist the mating, males leave.

Post‐copulatory Mounting Behavior of the West Indian Sweetpotato Weevil, Euscepes postfasciatus (Fairmaire) (Coleoptera: Curculionidae)

When two related species interbreed, their hybrid offspring frequently suffer from reduced fitness The genetics of hybrid incompatibility are described by the Bateson-Dobzhansky-Muller (BDM) model, where fitness is reduced by epistatic interactions between alleles of heterospecific origin Unfortunately, most empirical evidence for the BDM model comes from a few well-studied model organisms, restricting our genetic understanding of hybrid incompatibilities to limited taxa These systems are predominantly diploid and incompatibility is often complete, which complicates the detection of recessive allelic interactions and excludes the possibility to study viable or intermediate stages Here, we advocate research into non-model organisms with haploid or haplodiploid reproductive systems and incomplete hybrid incompatibility because (1) dominance is absent in haploids and (2) incomplete incompatibility allows comparing affected with unaffected individuals We describe a novel two-locus statistic specifying the frequency of individuals for which two alleles co-occur This approach to studying BDM incompatibilities requires genotypic characterization of hybrid individuals, but not genetic mapping or genome sequencing To illustrate our approach, we investigated genetic causes for hybrid incompatibility between differentiated lineages of the haplodiploid spider mite Tetranychus evansi, and show that strong, but incomplete, hybrid breakdown occurs In addition, by comparing the genotypes of viable hybrid males and inviable hybrid male eggs for eight microsatellite loci, we show that nuclear and cytonuclear BDM interactions constitute the basis of hybrid incompatibility in this species Our approach opens up possibilities to study BDM interactions in non-model taxa, and may give further insight into the genetic mechanisms behind hybrid incompatibility

/pdf/detection-of-genetic-incompatibilities-in-non-model-systems-n1uy5k3ym2.pdf

Detection of genetic incompatibilities in non-model systems using simple genetic markers: hybrid breakdown in the haplodiploid spider mite Tetranychus evansi

Yukie Sato

Papers

Different expression profiles of jasmonic acid and salicylic acid inducible genes in the tomato plant against herbivores with various feeding modes

Rules for Nest Sanitation in a Social Spider Mite, Schizotetranychus miscanthi Saito (Acari: Tetranychidae)

Testing for reproductive interference in the population dynamics of two congeneric species of herbivorous mites

Post‐copulatory Mounting Behavior of the West Indian Sweetpotato Weevil, Euscepes postfasciatus (Fairmaire) (Coleoptera: Curculionidae)

Detection of genetic incompatibilities in non-model systems using simple genetic markers: hybrid breakdown in the haplodiploid spider mite Tetranychus evansi