Sexually transmitted diseases (STDs) of insects are known from the mites, nematodes, fungi, protists and viruses. In total 73 species of parasite and pathogen from approximately 182 species of host have been reported. Whereas nearly all vertebrate STDs are viruses or bacteria, the majority of insect STDs are multicellular ectoparasites, protistans or fungi. Insect STDs display a range of transmission modes, with 'pure' sexual transmission only described from ectoparasites, all of which are mites, fungi or nematodes, whereas the microparasitic endo-parasites tend to show vertical as well as sexual transmission. The distribution of STDs within taxa of insect hosts appears to be related to the life histories of the hosts. In particular, STDs will not be able to persist if host adult generations do not overlap unless they are also transmitted by some alternative route. This explains the observation that the Coleoptera seem to suffer from more STDs than other insect orders, since they tend to diapause as adults and are therefore more likely to have overlapping generations of adults in temperate regions. STDs of insects are often highly pathogenic, and are frequently responsible for sterilizing their hosts, a feature which is also found in mammalian STDs. This, combined with high prevalences indicates that STDs can be important in the evolution and ecology of their hosts. Although attempts to demonstrate mate choice for uninfected partners have so far failed it is likely that STDs have other effects on host mating behaviour, and there is evidence from a few systems that they might manipulate their hosts to cause them to mate more frequently. STDs may also play a part in sexual conflict, with males in some systems possibly gaining a selective advantage from transmitting certain STDs to females. STDs may well be important factors in host population dynamics, and some have the potential to be useful biological control agents, but empirical studies on these subjects are lacking.

Summary Angiosperm genome sizes (GS) range c. 2400‐fold, and as nucleic acids are amongst the most phosphorus‐ (P) and nitrogen (N)‐demanding cellular biomolecules, we test the hypothesis that a key influence on plant biomass and species composition is the interaction between N and P availability and plant GS.We analysed the impact of different nutrient regimes on above‐ground biomass of angiosperm species with different GS, ploidy level and Grime's C‐S‐R (competitive, stress‐tolerant, ruderal) plant strategies growing at the Park Grass Experiment (Rothamsted, UK), established in 1856.The biomass‐weighted mean GS of species growing on plots with the addition of both N and P fertilizer were significantly higher than that of plants growing on control plots and plots with either N or P. The plants on these N + P plots are dominated by polyploids with large GS and a competitive plant strategy.The results are consistent with our hypothesis that large genomes are costly to build and maintain under N and P limitation. Hence GS and ploidy are significant traits affecting biomass growth under different nutrient regimes, influencing plant community composition and ecosystem dynamics. We propose that GS is a critical factor needed in models that bridge the knowledge gap between biodiversity and ecosystem functioning.

Summary 1.Since parasite transmission is often density-dependent, group living is normally thought to lead to an increased exposure to parasitism. As a consequence, it is predicted that animals living in groups will invest more resources (energy, time, risk, etc.) in parasite defence than those living solitarily. 2. We tested this prediction by measuring basal immune parameters in the larvae of 12 species of Lepidoptera, grouped into six phylogenetically matched species-pairs, each comprising one solitary feeding and one gregariously feeding species. 3. Contrary to expectation, the solitary species in all six species-pairs had higher total haemocyte counts than the gregarious species, and in five out of six species-pairs the solitary species also exhibited higher phenoloxidase activity. Both measurements were positively correlated with each other and with the magnitude of the cellular encapsulation response. 4. The relationship between infection risk and group living was investigated with a dynamic, spatially explicit, host-pathogen model. This shows that when individuals aggregate in groups, the per capita risk of infection can be reduced if the lower betweengroup transmission more than compensates for the higher within-group transmission. 5. We conclude that the expectation that group living always leads to increased exposure to pathogens and parasites is overly simplistic, and that the specific details of the social system in question will determine if there is increased or decreased exposure to infection.

. 1. Non-linear allometries are those where a log -log scatterplot of trait size against body size deviates from simple linearity. These are found in many insects, including the horns of beetles, the forceps of earwigs, and the heads of certain castes of ant.2. Non-linear allometries are often associated with polyphenism that is itself related to behaviour: for example, the alternative mating tactics displayed by many species of beetle are widely associated with dimorphisms in horn size.3. This paper critically reviews the current techniques used to analyse these datasets. 4. Recommendations include the use of scatterplots and assessment of the goodness of fit of simple linear models as an initial screen for non-linear allometry. The use of recently developed algorithms for 'segmented' regression to analyse continuous allometric relationships, and a pragmatic approach to the analysis of discontinuous relationships that recognises that there is no simple way to distinguish between morphs in some cases, and that all of the proposed methods for doing so have some drawbacks.5. Worked examples of the analysis of two sets of data from animals that have been the subject of controversy regarding the nature of their allometric relationships are given: further worked examples are provided as online Supporting Information .Key words . Allometry , Allomyrina , analysis , dimorphism , non-linear allometry , polyphenism , switchpoint , Onthophagus . the detection and further analysis of non-linear allometries, with particular emphasis on dimorphic allometries, and makes recommendations for the best way to analyse a variety of different sorts of such non-linear allometric relationships. The use of these analyses is illustrated by two worked examples, and three further worked examples are provided as online Supporting Information . Figure 1 shows scatterplots of non-linear allometries from three insect species. It is obvious from a glance at this figure that there is substantial variation in these relationships, and the form of the relationship is an important consideration in deciding which analysis to use. The simplest and most important division is into what can be called continuous and discontinuous allometries. Continuous allometries are those where the allometric relationship can be regarded as a single, albeit not necessarily straight, line. These allometries can include simple curved relationships ( Fig. 1a ), ones with a switchpoint where the slope of the relationship changes abruptly [as is claimed, for example, for the horned beetle Onthophagus binodis ( Cook, 1987 ; see also Supporting Information Example 1) and for the fig wasp Sycoscapter australis ( Bean & Cook, 2001 )] and also those that show sigmoid patterns such as Onthophagus taurus ( Fig. 1b ). Discontinuous allometries are those that are divided into two (or more) discontinuous groups, which may be more or less separated from each other and which are not adequately modelled by a continuous line. Such discontinuous allometries are described from ma...

Summary1. Previous theoretical models of the effect of sexual selection on average individual fitness in a population have mostly predicted that sexually selected populations should adapt faster and clear deleterious mutations more quickly than populations where sexual selection is not operating. 2. While some laboratory studies have supported these predictions, others have not and studies of field systems have tended to find negative effects of sexual selection, or no effect. The negative effects of sexual selection found in field and other studies are usually ascribed to the costs associated with strong sexual selection acting on the population. 3. Here, using an individual-based model that allows feedback between demographic and evolutionary processes, we find that sexual selection can lead to both increases and decreases in population-level fitness measures such as extinction probability and adaptation rate. Whether fitness increases or decreases depends on a variety of environmental and demographic factors including the nature of environmental change, the carrying capacity of the environment, the average fecundity of the population in question and the strength of condition dependence. 4. In many cases, our model predicts that sexual selection leads to higher extinction probability in small populations because of an increased risk of demographic stochasticity, but lower extinction probability in larger populations because of faster adaptation rates. This is consistent with field studies that have mostly focussed on very small populations such as recently introduced birds, and tend to find negative effects, and also with laboratory studies that tend to use larger populations and have tended to find positive effects. 5. These findings go at least some way towards an understanding of the apparent contradictions between theoretical predictions, laboratory studies and field data.

In some cases male animals engage in aggressive contests for access to females, in others they adopt more passive strategies and invest in traits that assist them in detecting females or in competing with rivals in other ways, such as sperm competition. One possible factor determining the fitness of these different strategies is population density. Theoretically, aggressive tactics should be found at intermediate population densities. At low densities males that invest in traits related to searching for mates could be favoured, whereas at the highest densities males that fight over females might pay excessive costs for this behaviour because of the number of rival males that they will encounter. Current empirical evidence is mostly consistent with this scheme: in some cases it seems that traits that are associated with locating mates are favoured at low densities, with aggression related traits favoured at higher densities, and in other cases aggression is selected but as density increases less aggressive strategies become more common. There remain substantial differences between species, however, and I discuss how variation in mating system, in the costs of aggression and in the nature of sperm competition, plus ecological differences between species, can change the relationship between population density and the fitness consequences of aggressive and passive behavioural strategies.

Many studies have demonstrated the adaptive advantage of elaborate secondary sexual traits, but few if any have shown compelling evidence for the limits to the elaboration of these traits that must exist. We describe such evidence in the exaggerated mandibles of stag beetles. In 1932, Huxley showed that the slope of the allometric relationship between mandible length and body size in some stag beetles declines in the largest males. We show that this curvature is most pronounced in species with relatively long mandibles, consistent with the hypothesis that the decrease in slope is caused by the increasing costs of large mandibles, which ultimately limit their size. Increasing depletion of resources in the prepupa and pupa by the rapidly growing mandibles is the most likely way in which these costs are manifested. The curved allometries have two components: intraspecific mandible allometry is steepest among small males of the species with the longest mandibles, but shallowest among the largest males of those same species. These patterns suggest that selection continues to favour positive allometry in species that invest relatively more in weaponry despite the limits to mandible exaggeration being reached in the largest males.

Many host‐parasite models assume that transmission increases linearly with host population density (‘density‐dependent transmission’), but various alternative transmission functions have been proposed in an effort to capture the complexity of real biological systems. The most common alternative (usually applied to sexually transmitted parasites) assumes instead that the rate at which hosts contact one another is independent of population density, leading to ‘frequency‐dependent’ transmission. This straight‐forward distinction generates fundamentally different dynamics (e.g. deterministic, parasite‐driven extinction with frequency‐ but not density‐dependence). Here, we consider the situation where transmission occurs through two different types of contact, one of which is density‐dependent (e.g. social contacts), the other density‐independent (e.g. sexual contacts). Drawing on a range of biological examples, we propose that this type of contact structure may be widespread in natural populations. When our model is characterized mainly by density‐dependent transmission, we find that allowing even small amounts of transmission to occur through density‐independent contacts leads to the possibility of deterministic, parasite‐driven extinction (and lowers the threshold for parasite persistence). Contrastingly, allowing some density‐dependent transmission to occur in a model characterized mainly by density‐independent contacts (i.e. by frequency‐dependent transmission) does not affect the extinction threshold, but does increase the likelihood of parasite persistence. The idea that directly transmitted parasites exploit different types of host contact is not new, but here we show that the impact on dynamics can be fundamental even in the simplest cases. For example, in systems where density‐dependent transmission is normally assumed de facto, we show that parasite‐driven extinction can occur if a small amount of transmission occurs through density‐independent contacts. Many empirical studies are still guided by the traditional density/frequency dichotomy, but our combined transmission function may provide a better model for systems in which both types of transmission occur.