THE EVOLUTION OF ALTERNATE MORPHOLOGIES: FITNESS AND WING MORPHOLOGY IN MALE SAND CRICKETS

Many organisms show distinct morphological types. We argue that the evolution of these alternate morphologies depends upon both fitness differences between morphs within each sex and the genetic correlation between sexes. In this paper, we examine the evolution of alternate morphologies using wing dimorphism in insects as a model system. Many insect species are wing dimorphic, one morph having wings and being capable of flight, the other lacking functional wings. While there is a well established trade-off in females between macroptery and reproduction, there are few data on the possible costs in males. We examine trade-offs between macroptery and life-history traits in male sand crickets, Gryllus firmus, and estimate the genetic correlation of wing dimorphism between the sexes. Macropterous males develop faster than micropterous males and are either larger or the same size depending upon rearing conditions. There is no difference in absolute or relative testis size at eclosion or 7 d thereafter. Finally, there is no difference between macropterous and micropterous males in relative success at siring offspring. Thus, with respect to the above traits, there are no costs associated with being winged in male G. firmus. It is possible that there may be a trade-off between calling rate and macroptery. A comparison of the relative frequency of macroptery between males and female across different orders of insects supports this hypothesis. The genetic correlation of wing dimorphism between the sexes is high (r₈ = 0.86), and hence the frequency of macroptery in males may be strongly influenced by selection acting on females.     

Food quality affects wing-form,demographic traits and number of yeast-like symbionts (YLS) in the planthopper vector,Delphacodes kuscheli (Hemiptera: Delphacidae)

Delphacodes kuscheli, the main vector of maize Mal de Río Cuarto disease in Argentina, was used to analyze the effect of food quality on wing-form, demographic traits and number of yeast-like symbionts (YLS). First instar nymphs were caged on the leaf apex or on the ligular zone of oat plants, characterized by having low and high nutritional value respectively, and followed in their development to adulthood. Food quality affected the proportion of wing morphs, with an increased number of brachypterous individuals on the higher food quality zone. Macropterous and brachypterous females from the ligular zone had higher survivorship, shorter development time and higher number of YLS. For males, development time and number of YLS did not differ significantly in individuals fed from both zones, while body and wing length were superior in individuals fed on the ligular zone. Results suggest that females allocate the resources from feeding on a richer zone to reduce the pre-reproductive period and to increase the number of YLS, and males acquire a larger size while maintaining development time and YLS number. This is the first study quantifying the variation of number of YLS according to food quality in a Neotropical planthopper pest.     

EVIDENCE THAT THE MAGNITUDE OF THE TRADE-OFF IN A DICHOTOMOUS TRAIT IS FREQUENCY DEPENDENT

Many traits, such as wing dimorphism, paedomorphosis, and cyclomorphosis vary dichotomously. Such dimorphisms are maintained in part because of a trade-off between components of fitness: for example, in insects, the flightless morph cannot migrate but has a greater fecundity than the flight-capable morph. Several recent theoretical studies have analyzed the evolution of dichotomous traits, assuming that each morph can be characterized by a discrete syndrome of characters. Consideration of the genetic basis of dimorphism suggests that this assumption is incorrect. In this paper, I report a test of this assumption using the wing-dimorphic sand cricket, Gryllus firmus. It is predicted that, rather than remaining constant, the fecundity of macropterous (long-winged, flight-capable) females will decrease as the proportion of macropterous females in the population or family increases. This prediction is supported by fecundity data from lines selected for high and low proportions of macroptery and by sib analysis. Thus, models that seek to predict the evolution of dichotomous traits should take into account the likelihood that values of components of fitness, such as fecundity, may be related to their frequencies in the population.     

Dispersal capability in a habitat specialist bush cricket: the role of population density and habitat moisture

1. In fragmented landscapes many insect species depend on a regular exchange of individuals between subpopulations to ensure the persistence of the population. Thus, the ability to disperse is of particular relevance. 2. However, in some insect species mobility is not a fixed trait. Hence, knowing the causes of phenotypic plasticity is of great importance when evaluating whether a species is able to survive in fragmented landscapes or not. 3. A multi‐year field study was conducted to identify possible causes of macroptery in the wing‐dimorphic habitat specialist Metrioptera brachyptera L. and to quantify its dispersal capability (% macropters). Therefore, 746 individuals of the species were caught on 135 plots. Additionally, environmental variables that possibly induce the development of macropters (population density and habitat moisture) were recorded. 4. Dispersal capability of M. brachyptera was very low. Less than 3% were long‐winged. The statistical analysis revealed that the proportion of long‐winged M. brachyptera was strongly correlated with high bush‐cricket densities and not with habitat moisture. 5. The low dispersal capability of M. brachyptera leads to the conclusion that individual exchange between isolated populations is limited or even impossible. Habitat specialists, like M. brachyptera, may thus be unable to respond to rapid changes in the availability of suitable habitats by dispersing, and hence may be especially dependent on habitat management activities that promote the long‐term stability of existing habitat patches.