Morphology of Parasitengona mites (Acariformes: Parasitengona) and their possible evolutionary scenario

On the basis of the analysis of morphology and biology of representatives of the Parasitengona, mostly trombiculids, trombidiids and water mites, a new attempt is made to clarify probable evolutionary scenario in this group of the higher trombidiform mites (Actinedida). It is supposed that the very old ancestral group of terrestrial arachnids, having bite-sucking mouth-parts, poorly differentiated sac-like midgut and capability to extra-oral digestion, fed predatory on different small soil arthropods at all phases of the life cycle. They were small segmented orthotrichous homeomorphic arachnids at the rank of genus or family. The favorable feeding conditions of the adult phase have led to the small eggs rich in yolk and the small larva. The latter have led in turn to the necessity of intensive feeding at the larval stage to complete the ontogenesis. Further in evolution, this group gave rise at once to two or even more large paraphyletic branches. Most of them retained feeding on arthropods with transition of larvae to much more effective parasitic feeding provided with the additional specialization of the larval stage. This branch comprise divergently radiated paraphyletic terrestrial and secondary-water water mites each having long course of evolution resulted in the recent groups of Calyptostomatoidea, Erythraeoidea, Trombidioidea and several superfamilies of water mites. Another branch of the ancestral Parasitengona has followed the way of adaptation of larvae to feeding on vertebrates, which were being attacked by the larvae in the environment of pasture. The parasitism on vertebrates has lead to several radical specializations of these mites and their significant evolutionary progress. At the same time, the similar ontogenetic dynamics, as well as synchronous reduction of particular developmental stages in all parasitengones, inevitably indicate the monophyletic origin of the whole branch of Parasitengona with Pterygosomatidae as the most probable sister group.     

Loss of larval parasitism in parasitengonine mites

Larval Parasitengona are typically parasites, yet at least 29 species of water mites and one species of Trombidiidae forgo larval feeding and any association with a host. Species with non-feeding larvae are isolated cases within species groups or genera where the remaining species have parasitic larvae. Species without larval parasitism occur in at least 14 genera, eight families and four superfamilies of water mites; the loss of larval parasitism is presumably polyphyletic, having occurred at least 21 times. Lineages of water mites with non-feeding larvae frequently exist in parallel with almost identical populations or species that have parasitic larvae. Thus, there is tremendous potential for studies comparing the relative merits of the two life history strategies. Comparisons indicate that adults from lineages with non-parasitic larvae produce smaller numbers of larger eggs; the extra nutrition included in larger eggs permits the larvae to forgo feeding. Non-feeding larvae frequently have wider dorsal plates but reduced leg length, setal length and sclerotization when compared to parasitic larvae from sister lineages. The adults of lineages with non-feeding larvae are frequently smaller in comparison to adults of sister lineages with parasitic larvae. There is no apparent pattern in relation to habitat: lineages lacking larval parasitism occur in streams, temporary ponds and the littoral and planktonic regions of permanent lakes. © Rapid Science Ltd. 1998     

The origin of parasitism in trombiculid mites (Acariformes: Trombiculidae)]

On the basis of literary data and original investigations some phylogenetic, ecological and morphological aspects of the origin of parasitism in trombiculid mites are carefully considered for the first time. It is shown that parasitism in this group of trombidiform mites is a relatively young historical phenomenon and was formed after their ontogenesis had differentiated into active and quiescent stages. Therefore, in the life pattern of trombiculid mites the character of individual development, that defines their biotopical restriction, is much more important than the phase parasitism. Primitive organization of the digestive system and extraintestinal digestion, so characteristic of this group, are one of the main reasons of the origin of their parasitism. Under pasture conditions trombiculid mites, that initially were predators-entomophages with bite-sucking mouth parts, pass easily to parasitism on vertebrate animals and become primary lymphophages. They use the vertebrate host's organism exclusively as a source of food and by the extent of polyphagia are very close to free-living blood-sucking insects. Stylostome, that develops during feeding of trombiculid larvae and some other closely related groups of trombidiform mites, is a universal structure for achieving a large amount of food on a wide range of animals during a relatively short period of time and reflects wide host-parasite specificity of these parasitic mites. From the historical view the larvae of trombiculid mites did not pass from one group of hosts to the others, but owing to morphological preadaptation to parasitism passed in a definite historical period, not earlier than Paleogene, to parasitism on all classes of terrestrial vertebrates, especially on mammals, their primary hosts.     

External structure of cuticle injuries and larval mouth parts of the chiggers Euschoengastia rotundata and Neotrombicula vulgaris (Trombiculidae)

When E. rotundata larvae parasitize the abdominal part of the body of their host (Clethrionomys glareolus), capsules with round terminal opening are formed from which hind part of the mite's body projects forwards. Organization of the capsules shows that their walls are formed by a substance (probably by larval saliva) which differs from host's tissues. At the bottom of the capsules there are larval adhesive sites with openings in the proximal parts of stylostomes which resemble in their structure these of N. vulgaris larvae. The latter do not form capsules when feeding on their natural hosts, Microtus arvalis. Proximal part of stylostome is formed in both cases by amorphous glutinous substance bearing imprints of mite's mobile digits of chelicerae and hypostome. Mouth parts of hungry mites and satiated larvae of both species differ only in relative sizes of constituent parts. Soft apical part of hypostome turns backwards during the feeding and forms a sucker. The feeding of larvae of trombiculids in capsules, which is formally regarded as ectoparasitism, can apparently be considered as a special type of parasitism.     

Parasitism of mosquitoes (Diptera: Culicidae) by larval mites (Acari: Parasitengona) in Adelaide, South Australia

Larval mites (Acari) from the cohort Parasitengona were collected from adult female mosquitoes captured in Adelaide, South Australia, from 1997 to 2000. Larvae from three families were identified: Arrenuridae, Hydryphantidae and Erythraeidae. Arrenurid larvae were associated with mosquitoes that use ground pools for larval habitat, while hydryphantids were associated with tree-hole and container-breeding species. Only a single erythraeid record was made. The overall prevalence of parasitism was very low (0.27% of 19 280 mosquitoes) and ranged from 0 to 5.6% for the 16 mosquito species collected. New mite–host records are presented.     

Resting nymphal stages and the nature of individual development in trombiculid mites (Acariformes: Trombiculidae)

A morphological expression of quiescent nymphal instars (calyptostases) in trombiculid mites (Trombiculidae) is analysed. The analysis takes into consideration ontogenetic functions of different instars during the individual development of these mites, which includes an alternation of active and regressive quiescent instars. Cyclic start and blocking of different integumental differentiation programs in Trombiculidae is caused by the cyclic reduction and renewal of particular functions of respective instars, whereas internal organs of these mites do not transform significantly during the life cycle. The reduction of some functions, particularly the locomotion and feeding, in the quiescent nymphal instars with changed integumental function has an inevitable result in a complication and prolongation of the moulting process. The moulting of these instars begins at once after finishing the previous moulting cycle, i.e. it is realized in "automatic pattern" without the intermoult phase. In general, the organization of both quiescent proto- and tritonymph is the same, because it expresses concordant morphological correlations and synchronous reductions of certain functions and structures in these instars during the evolutionary process. At the same time, the trombiculid mites and, perhaps, other representatives of Parasitengona reveal the most generalized type of ontogenesis in Acariformes within the "alternating calyptostasy" phenomenon.     

Differential Water Mite Parasitism,Phenoloxidase Activity,and Resistance to Mites Are Unrelated across Pairs of Related Damselfly Species

Related host species often demonstrate differences in prevalence and/or intensity of infection by particular parasite species, as well as different levels of resistance to those parasites. The mechanisms underlying this interspecific variation in parasitism and resistance expression are not well understood. Surprisingly, few researchers have assessed relations between actual levels of parasitism and resistance to parasites seen in nature across multiple host species. The main goal of this study was to determine whether interspecific variation in resistance against ectoparasitic larval water mites either was predictive of interspecific variation in parasitism for ten closely related species of damselflies (grouped into five “species pairs”), or was predicted by interspecific variation in a commonly used measure of innate immunity (total Phenoloxidase or potential PO activity). Two of five species pairs had interspecific differences in proportions of individuals resisting larval Arrenurus water mites, only one of five species pairs had species differences in prevalence of larval Arrenurus water mites, and another two of five species pairs showed species differences in mean PO activity. Within the two species pairs where species differed in proportion of individuals resisting mites the species with the higher proportion did not have correspondingly higher PO activity levels. Furthermore, the proportion of individuals resisting mites mirrored prevalence of parasitism in only one species pair. There was no interspecific variation in median intensity of mite infestation within any species pair. We conclude that a species’ relative ability to resist particular parasites does not explain interspecific variation in parasitism within species pairs and that neither resistance nor parasitism is reflected by interspecific variation in total PO or potential PO activity.     

Conflict between antipredator and antiparasite behaviour in larval damselflies

 Larval damselflies resist infestation by parasitic larval mites by exhibiting behaviours such as grooming, crawling, swimming, and striking at host-seeking mites. Larval damselflies are known to increase time spent in these behaviours in the presence of mites but reduce time spent in these behaviours in the presence of fish predators. The presence of both fish and larval mites presents an obvious conflict: a larval damselfly may actively avoid parasitism by mites, thus increasing its risk of predation, or it may reduce its activity when fish are present, thus increasing its risk of parasitism. We analysed the behaviour of larval Ischnura verticalis in an experiment where we crossed presence and absence of fish with presence and absence of larval mites. Presence of mites induced a large increase in activity of larval I. verticalis but fish had no effect and there were no interpretable interactions between effects of mites and fish. Subsequent experiments indicated that larval I. verticalis in the presence of both mites and fish were more likely to be attacked and killed by fish than those exposed only to fish. The high activity level of I. verticalis larvae in the presence of both fish and mites may suggest that costs of parasitism are high, or that under field conditions it is rare for larvae to be in the immediate presence of both fish predators and potentially parasitic mites. Received: 28 March 1996 / Accepted: 6 September 1996     

Modelling parasitism and predation of mosquitoes by water mites

Parasitism and predation are two ecological interactions that can occur simultaneously between two species. This is the case of Culicidae (Insecta: Diptera) and water mites (Acari: Hydrachnidia). The larva mites are~parasites of aquatic and semiaquatic insects, and deutonymphs and adults are predators of insect larvae and eggs. Since several families of water mites are associated with mosquitoes there is an interest in the potential use of these mites as biological control agents. The aim of this paper is to use mathematical modelling and analysis to assess the impact of predation and parasitism in the mosquito population. We propose a system of ordinary differential equations to model the interactions among the larval and adult stages of mosquitoes and water mites. The model exhibits three equilibria: the first equilibrium point corresponds to the state where the two species are absent, the second one to the state where only mosquitoes are present (water mites need insects to complete their life cycle), and the third one is the coexistence equilibrium. We analyze conditions for the asymptotic stability of equilibria, supported by analytical and numerical methods. We discuss the different scenarios that appear when we change the parasitism and predation parameters. High rates of parasitism and moderate predation can drive two species to a stable coexistence.     

Possible evolutionary scenarios in the parasitengona mites (Acariformes: Parasitengona) based on anatomical peculiarities of their digestive system

Five possible evolutionary scenarios of the higher acariform mites from the cohort Parasitengona are proposed on the basis of the detailed examination of anatomy of the excretory organ and midgut in the representatives of terrestrial mite families Trombiculidae and Microtrombidiidae, and in freshwater mite families Teutoniidae and Pionidae, on different developmental stages including parasitic larva. These scenarios explain possible ways of evolutionary transformation within the Parasitengona from one or several ancestor with the open digestive tract.     

A review of the external morphology of the family pterygosomatidae and its systematic position within the Prostigmata (Acari: Acariformes)

According to the traditional views mites of the family Pterygosomatidae belong to the cohort Anystina (Krantz, 1978; Kethley, 1982). Kethley (1982), however, noted similarities between these mites and representatives of the cohort Eleutherengona. In the tree diagram suggesting relationships among higher taxa Prostigmata proposed by Kethley (in Norton et al., 1993) this family derives from the eleutherengone clade. However, the characters and ranges of taxa upon which Kethley's hypothesis was based were not stated. In this paper, the external morphology of pterygosomatid mites is analyzed. The data provide strong evidence supporting a close relationship between Pterygosomatidae and the eleutherengone mites (Raphignathae and Heterostigmata). The setation of Pterygosomatidae is similar that of Raphignathae by the absence of trichobothria, adanal setae, and by the strongly reduced leg setation. In these mites, as in the eleutherengones (Raphignathae) an aedeagus is present, in females, the genital and anal openings are situated close to each other and are covered by a pair of common folds, in males these openings are fused, the leg femora are not separated onto basi- and telofemur, the naso, sejugal furrow, genital papillae, and the larval Claparede's organs are absent. Some similarities in the structure of the gnathosoma and the chelicerae with Anystina (including Parasitengona) are, probably, symplesiomorphies or convergently developed. Moreover, in pterygosomatids, the gnathosomal setation is represented by a single pair of gnathobasal setae, and the cheliceral and adoral setae, present in anystoid mites and early derivative eleutherengones, are absent. We believe, therefore, that Pterygosomatidae is a separate branch within the cohort Eleutherengona. Its exact position is, however, still unclear. Among pterygosomatid genera, mites of the genus Pimeliaphilus, which possess the maximal setation, are closest to the habitus. These mites are known from different parts of the world parasitizing mostly secretively living arthropods. We suggest that ancestors of the family were initially associated with arthropods and parasitism of pterygosomatids on lizards is the result of host switching from arthropods to these hosts.     

Red, distasteful water mites: did fish make them that way?

Water mites (Acari: Hydrachnida) are unusual among the typically cryptic freshwater fauna in that many species are brightly colored red or orange, and also appear to be distasteful to fish. This apparent aposematism (use of color to warn predators) has been previously explained as the evolutionary end-product of pressure from fish predation. The fish-predation argument has been supported by observations that fish spit out red mites, powder made from red water mites is more distasteful to fish than powder made from non-red mites, and red mites appear to be more abundant than non-red mites in water bodies where fish are present. In this paper, we challenge the hypothesis that fish were the sole driving force behind the evolution of aposematism in water mites. We show that non-red mites actually dominate in water bodies with fish, and that red mites are more abundant in temporary, fishless water bodies. We also demonstrate that powder made from red, terrestrial velvet mites (Trombidiidae) was as distasteful to fish as powder made from red water mites. We suggest that the main role of red and orange carotenoid pigments may be to act as photoprotectants, and hypothesize that redness originated in the terrestrial ancestors of water mites and has been retained in certain lineages of water mites after the invasion of the aquatic habitat. We also suggest that distastefulness evolved subsequent to bright coloration in response to increased conspicuousness to predators. Relaxed selection for redness has occurred when adults and/or larvae are less exposed to sunlight, either through occupying more protected habitats, parasitizing more nocturnal hosts, or parasitizing hosts for a short period of time. Our ability to test this alternative hypothesis is hampered by lack of knowledge of the source and mode of action of distastefulness, and of phylogenetic relationships among the Parasitengona.     

Life cycle and parasitic interaction of the lizard-parasitizing mite Ophionyssus galloticolus (Acari: Gamasida: Macronyssidae), with remarks about the evolutionary consequences of parasitism in mites

Wild-caught specimens of the lacertid lizard Gallotia galloti eisentrauti from the Canary Island of Tenerife were checked for ectoparasites. The parasitic gamasid mite Ophionyssus galloticolus Fain and Bannert (2000) was very abundant on these lizards. Additionally, parasitism by larvae of two species of Trombiculidae (Prostigmata: Parasitengona) was observed. O. galloticolus was reared in the laboratory on its natural host in order to investigate its life cycle, reproductive biology, and development. The life history of O. galloticolus is documented in detail and compared to literature data of other Ophionyssus species. O. galloticolus was found to be similar to other species of the same genus with respect to the duration of development, the precopulatory association of protonymphs, and the arrhenotokous development of eggs. However, it seems to be more tolerant towards low relative humidity and longer starvation periods than other Ophionyssus species. Evolutionary transformations of the life-history pattern of this genus and other parasitic mites in comparison to its predatory precursors involve a reduction or partial suppression of ontogenetic instars in order to decrease mortality during host-seeking phases, and a compensating increase in growth capacity of the remaining feeding instars facilitated by replacement of sclerites through elastic cuticle or by growth of new cuticle unrelated to a moult (neosomy).     

Red, distasteful water mites: did fish make them that way?

Water mites (Acari: Hydrachnida) are unusual among the typically cryptic freshwater fauna in that many species are brightly colored red or orange, and also appear to be distasteful to fish. This apparent aposematism (use of color to warn predators) has been previously explained as the evolutionary end-product of pressure from fish predation. The fish-predation argument has been supported by observations that fish spit out red mites, powder made from red water mites is more distasteful to fish than powder made from non-red mites, and red mites appear to be more abundant than non-red mites in water bodies where fish are present. In this paper, we challenge the hypothesis that fish were the sole driving force behind the evolution of aposematism in water mites. We show that non-red mites actually dominate in water bodies with fish, and that red mites are more abundant in temporary, fishless water bodies. We also demonstrate that powder made from red, terrestrial velvet mites (Trombidiidae) was as distasteful to fish as powder made from red water mites. We suggest that the main role of red and orange carotenoid pigments may be to act as photoprotectants, and hypothesize that redness originated in the terrestrial ancestors of water mites and has been retained in certain lineages of water mites after the invasion of the aquatic habitat. We also suggest that distastefulness evolved subsequent to bright coloration in response to increased conspicuousness to predators. Relaxed selection for redness has occurred when adults and/or larvae are less exposed to sunlight, either through occupying more protected habitats, parasitizing more nocturnal hosts, or parasitizing hosts for a short period of time. Our ability to test this alternative hypothesis is hampered by lack of knowledge of the source and mode of action of distastefulness, and of phylogenetic relationships among the Parasitengona.     

Parasitism ofAcyrthosiphon pisum byAllothrombium pulvinum (Acariformes: Trombidiidae): Host attachment site,host size selection,superparasitism and effect on host

Several aspects of parasitism of the pea aphid,Acyrthosiphon pisum (Harris), by the mite parasiteAllothrombium pulvinum Ewing, were examined in the laboratory. Larvae ofA. pulvinum were fastmoving mites that find their host by contact of their foretarsi with the host. They can attach to all parts of the host body, but insert their chelicerae only into weakly sclerotized parts such as intersegmental membranes. Of the attached larval mites, most (63.5–74.1%) were on the thorax of their hosts, regardless of host size. In hosts of small and medium size, the ventral side receives most parasitism, whereas in large hosts the lateral sites are most often attacked. Larval mites prefer large hosts when allowed to select between pairs of large and small hosts, but show no significant preference when allowed to choose between pairs of large and medium hosts or pairs of medium and small hosts. In two-choice tests, larval mites prefer previously parasitized hosts to umparasitized hosts, which results in superparasitism of the hosts. When the mite load is fiveA. pulvinum kills all small hosts within three days, and all medium hosts and 50% of large hosts within four days, the reproduction of surviving adult aphids were significantly reduced. Host-finding behavior, attachment site preference, host size selection, superparasitism, and effect on hosts are briefly reviewed for larval parasites of Trombidiidae. The potential role of larvalAllothrombium in integrated and biological aphid control is also discussed.     

Larval parasitism of spring-dwelling alpine water mites (Hydrachnidia,Acari): a study with particular reference to chironomid hosts

During faunistic investigations on spring habitats in the alpine National Park Berchtesgaden (Bavaria, Germany), water mites were found to be the group with the highest share of species strongly adapted to springs. At four sample sites at two spring complexes, insect emergence was screened for parasitism by larval water mites. A total of at least 36 host species were recorded as being parasitized by 19 water mite species. As in many other habitats, the most important host taxon was shown to be the nematoceran family Chironomidae, both in the number of species and individuals parasitized. Likewise, the number of water mite species attached to chironomids was high. Further host species were found among the Plecoptera, Trichoptera, Coleoptera, Limoniidae and Empididae (Diptera). These taxa were only parasitized by a single water mite species in each case. For 13 mite species, new hosts were recorded for the first time. For another six species, the known host spectrum could be confirmed and/or supplemented. The parasitological data presented (e.g., prevalences, selected attachment sites on the host, larval phenology, intensity of parasitism) provide, in most cases, basic information concerning previously unknown parasite–host associations. At this time, the reason for the strong crenobiosis in water mites cannot be explained by their parasitism.     

Types of parasitism of acarines and insects on terrestrial vertebrates

According to the recent taxonomic revisions, over 40000 species of insects and acarines are parasites or micropredatory blood-suckers of mammals and birds. The largest fraction of them are micropredators and temporary or permanent ectoparasites, the minority being endoparasitic. Some arthropods (blood-sucking dipterans) use the host primarily as a food resource, whereas for others (many astigmatic mites) the host constitutes the entire environment. A number of life forms, or types of parasitism, have arisen in the insects and acarines in the course of their adaptive evolution to parasitism on terrestrial vertebrates. The term “type of parasitism” designates a set of convergently arising morpho-physiological and ecological adaptations (adaptive complexes), demonstrated by different arthropod taxa. A classification of the types of parasitism in arthropods is proposed based on their temporal, spatial, and trophic associations with vertebrates. The following seven types of parasitism are distinguished: micropredatory blood-suckers, nest ectoparasites (nidicoles), temporary ectoparasites with prolonged feeding, permanent ectoparasites, intracutaneous endoparasites, cavity endoparasites, and tissue endoparasites.     

Parasites physically block host copulation: a potent mechanism of parasite-mediated sexual selection

Research on the role of parasites in sexual selection has focusedmainly on host mate choice favoring relatively unparasitizedmales. But parasites can also generate variance in host reproductivesuccess by influencing the ability of individual hosts to directlycompete among themselves for mates or fertilizations, a subjectarea that has received far less attention. We demonstrate experimentallythat parasitism by mites can drive sexual selection by way ofa novel mechanism involving male competition: physical inhibitionof host copulation. Mite resistance in natural populations isheritable, emphasizing the evolutionary potential of parasite-mediatedsexual selection in this system and indicating that femalesshould be receiving indirect fitness benefits as a result ofthis process. We show that parasitism by mites, Macrochelessubbadius, reduces mating success of male Drosophila nigrospiracula.Smaller males were more strongly compromised, identifying hostbody size as a tolerance trait. As parasite load increased,the rate at which males attempted to copulate but failed becauseof obstruction by mites increased. When mites were removed frominfested males, host mating success was restored. Thus, thephysical presence of the mites per se generates differentialmating success, in this case by interrupting the normal flowof mating behaviors. This study elucidates a potent mechanismof parasite-mediated sexual selection in a system wherein parasiteresistance is demonstrably heritable, and as such expands ourunderstanding of the evolutionary potential of sexual selection.     

EVOLUTIONARY LOSS OF LARVAL FEEDING: DEVELOPMENT,FORM AND FUNCTION IN A FACULTATIVELY FEEDING LARVA,BRISASTER LATIFRONS

Species with large eggs and nonfeeding larvae have evolved many times from ancestors with smaller eggs and feeding larvae in numerous groups of aquatic invertebrates and amphibians. This change in reproductive allocation and larval form is often accompanied by dramatic changes in development. Little is known of this transformation because the intermediate form (a facultatively feeding larva) is rare. Knowledge of facultatively feeding larvae may help explain the conditions under which nonfeeding larvae evolve. Two hypotheses concerning the evolutionary loss of larval feeding are as follows: (1) large eggs evolve before modifications in larval development, and (2) the intermediate form (facultatively feeding larva) is evolutionarily short-lived. I show that larvae of a heart urchin, Brisaster latifrons, are capable of feeding but do not require food to complete larval development. Food for larvae appears to have little effect on larval growth and development. The development, form, and suspension feeding mechanism of these larvae are similar to those of obligate-feeding larvae of other echinoids. Feeding rates of Brisaster larvae are similar to cooccurring, obligate-feeding echinoid larvae but are low relative to the large size of Brisaster larvae. The comparison shows that in Brisaster large egg size, independence from larval food, and relatively low feeding rate have evolved before the heterochronies and modified developmental mechanisms common in nonfeeding echinoid larvae. If it is general, the result suggests that hypotheses concerning the origin of nonfeeding larval development should be based on ecological factors that affect natural selection for large eggs, rather than on the evolution of heterochronies and developmental novelties in particular clades. I also discuss alternative hypotheses concerning the evolutionary persistence of facultative larval feeding as a reproductive strategy. These hypotheses could be tested against a phylogenetic hypothesis.     

The effects of selection for larval behavior on adult life-history features in Drosophila melanogaster

Selection for late-life fecundity and longevity in adult Drosophila melanogaster is well known to modify numerous characteristics of life history and physiology. We report experiments here in which selection applied to behavior affects features in an identical fashion. Selection for feeding rate of larval D. melanogaster modifies caloric intake, as measured by the uptake and incorporation of labeled glucose. Selection for slow larval feeding produced lines of D. melanogaster in which larvae synthesized significantly less lipid prior to pupation and eclosed to have low early-life fecundity and a long life as adults. They also had greater lifetime fecundity, but lower viability of egg to hatched adult. Alternatively, fast-feeding larvae incorporated more lipid before pupation and eclosed with high early-fecundity that declined rapidly throughout their short adult life. Slow-feeding populations also had a significantly enhanced expression of the stress-resistance genes CuZn-SOD, CATALASE, and HSP70. Selection on larval feeding behavior reproduced the antagonistic evolutionary trade-off found under selection for adult life span and mimicked the physiological response in life span as seen in many species when dietary restriction is imposed on adults. Thus, nutrient acquisition during development appears to share a common evolutionary and genetic basis with the allocation processes that determine adult life-history traits and the related phenotypic dietary restriction phenomena.