Structure and evolution of the stigmapophysis—A unique repose wing-coupling structure in Psocodea

The gain of foldable wings is regarded as one of the key innovations enabling the present-day diversity of neopteran insects. Wing folding allows compact housing of the wings and shields the insect body from damage. Wing-fixing systems have evolved in some insects, probably to increase the durability of the shielding function by the wings. Bark lice (Psocodea) are known to possess a unique wing-to-wing repose coupling system, but a detailed morphological and evolutionary study of this system is lacking. In this study, we examined this repose coupling structure by SEM in 32 species including representatives of all three suborders of bark lice (Trogiomorpha, Troctomorpha and Psocomorpha). We concluded that the repose wing-coupling apparatus independently evolved twice within Psocodea. In Trogiomorpha, the apparatus is located on the subcostal vein of the forewing and is composed of elongated rib-like structures. In Troctomorpha and Psocomorpha, in contrast, the repose coupling structure is located on the radius vein of the forewing and is formed by a swollen vein. These morphological and developmental differences in the repose coupling structures also provide phylogenetic information at different systematic levels.     

Evaluating the life‐history trade‐off between dispersal capability and reproduction in wing dimorphic insects: a meta‐analysis

A life‐history trade‐off exists between flight capability and reproduction in many wing dimorphic insects: a long‐winged morph is flight‐capable at the expense of reproduction, while a short‐winged morph cannot fly, is less mobile, but has greater reproductive output. Using meta‐analyses, I investigated specific questions regarding this trade‐off. The trade‐off in females was expressed primarily as a later onset of egg production and lower fecundity in long‐winged females relative to short‐winged females. Although considerably less work has been done with males, the trade‐off exists for males among traits primarily related to mate acquisition. The trade‐off can potentially be mitigated in males, as long‐winged individuals possess an advantage in traits that can offset the costs of flight capability such as a shorter development time. The strength and direction of trends differed significantly among insect orders, and there was a relationship between the strength and direction of trends with the relative flight capabilities between the morphs. I discuss how the trade‐off might be both under‐ and overestimated in the literature, especially in light of work that has examined two relevant aspects of wing dimorphic species: (1) the effect of flight‐muscle histolysis on reproductive investment; and (2) the performance of actual flight by flight‐capable individuals.     

Trade‐offs to flight capability in Gryllus firmus: the influence of whole‐organism respiration rate on fitness

Wing dimorphism, where some macropterous long‐winged (LW) individuals can fly whereas micropterous short‐winged (SW) individuals cannot, is common in insects and believed to be maintained in part by trade‐offs between flight capability and reproductive traits. In this paper we examine differences in whole‐organism respiration rate between wing morphs of the sand cricket Gryllus firmus. We hypothesized that maintenance of the flight apparatus would result in elevated CO₂ respired because of the high metabolic cost of these tissues, which, in turn, constrain resources available for egg production in females. As the trade‐off involves calling behaviour in males, we predicted no equivalent constraint on organ development in this sex. We found female macropters (particularly older crickets) had significantly higher residual respiration rates than micropters. In males, we found only marginal differences between wing morphs. In both sexes there was a highly significant effect of flight muscles status on residual respiration rate, individuals with functional muscles having higher respiration rates. Both female and male macropters had significantly smaller gonads than micropters. Whole‐organism residual respiration rate was negatively correlated with fecundity: macropterous females with high respiration rates had smaller gonads compared with macropterous females with lower respiration rates.     

Density‐dependent sex‐biased development of macroptery in a water strider

In wing‐polymorphic insects, wing morphs differ not only in dispersal capability but also in life history traits because of trade‐offs between flight capability and reproduction. When the fitness benefits and costs of producing wings differ between males and females, sex‐specific trade‐offs can result in sex differences in the frequency of long‐winged individuals. Furthermore, the social environment during development affects sex differences in wing development, but few empirical tests of this phenomenon have been performed to date. Here, I used the wing‐dimorphic water strider Tenagogerris euphrosyne to test how rearing density and sex ratio affect the sex‐specific development of long‐winged dispersing morphs (i.e., sex‐specific macroptery). I also used a full‐sib, split‐family breeding design to assess genetic effects on density‐dependent, sex‐specific macroptery. I reared water strider nymphs at either high or low densities and measured their wing development. I found that long‐winged morphs developed more frequently in males than in females when individuals were reared in a high‐density environment. However, the frequency of long‐winged morphs was not biased according to sex when individuals were reared in a low‐density environment. In addition, full‐sib males and females showed similar macroptery incidence rates at low nymphal density, whereas the macroptery incidence rates differed between full‐sib males and females at high nymphal density. Thus complex gene‐by‐environment‐by‐sex interactions may explain the density‐specific levels of sex bias in macroptery, although this interpretation should be treated with some caution. Overall, my study provides empirical evidence for density‐specific, sex‐biased wing development. My findings suggest that social factors as well as abiotic factors can be important in determining sex‐biased wing development in insects.     

Seasonal changes in the flight apparatus of winged females and sexual males of the aphid <Emphasis Type="Italic">Tuberculatus quercicola</Emphasis> (Hemiptera: Aphididae)

Tuberculatus quercicola (Matsumura) feeds on Quercus dentata Thunberg, and has mutualistic interactions with ants. Tuberculatus quercicola has two winged morphs in its life cycle, winged females appear in summer and sexual males appear in autumn. Previous studies have shown that wing loading (ratio of body volume to wing area) is higher for the winged females, because of ant attendance, resulting in extremely low dispersal. It is known that the nutritional quality of host plants is high in spring and autumn, when leaves are growing or senescent, and low in summer when leaves are mature. This study examined the effects of seasonal plant deterioration on the development of flight apparatus (wing size and flight muscle) of winged females and males. Moreover, field intercept traps were used to examine the extent of dispersal of males. The results showed that seasonal plant deterioration affected development of the flight apparatus of winged females, particularly flight muscle. Flight muscle development was significantly higher in winged males in autumn than in winged females. However, winged males were not caught in any of the traps. The different resource allocation to the flight apparatus of winged females and males is discussed.     

Trade‐off between flight capability and reproduction in male Velarifictorus asperses crickets

1. There are numerous data that support the trade‐off between flight capability and reproduction in female wing polymorphic insects, but the relationship between wing form and fitness remains poorly investigated in males. 2. In the present study, the development of flight muscle and gonads, spermatophore size, and multiple copulation ability were investigated in both long‐winged (LW) and short‐winged (SW) males to verify this trade‐off, using a wing dimorphic cricket species Velarifictorus aspersus (Walker). 3. The LW males had better‐developed wing muscles than the SW males on the day of emergence, and both of them developed wing muscles after emergence, but the peak of weight in SW males was achieved 4 days later than that of the LW males. The accessory glands (AG) of the LW males developed significantly slower than that of the SW males. These results suggest that development and maintenance of flight muscles have a cost on the development of reproductive organs in male V. asperses. 4. The SW males produced significantly heavier spermatophores in a single copulation and mated more often than LW males. This indicates the SW males have a higher mating success than the LW males, thereby increasing their chance of siring offspring.     

Molecular systematics of the bark lice infraorder Caeciliusetae (Insecta: Psocodea)

The phylogenetic relationships of bark lice and parasitic lice (Insecta: Psocodea) have been studied in a number of recent molecular phylogenetic analyses based on DNA sequences. Many of these studies have focused on the position of parasitic lice within the free‐living bark lice. However, fewer such studies have examined the relationships among major groups of free‐living bark lice and their implications for classification. In this study we focus on the infraorder Caeciliusetae, a large group of bark lice (?1000 species) within the suborder Psocomorpha. Using sequences of two mitochondrial and two nuclear genes, we estimated the phylogeny for relationships among the five recognized families within the infraorder Caeciliusetae. Based on the results, the sister‐group relationship and respective monophyly of Stenopsocidae and Dasydemellidae is strongly supported. Monophyly of the larger families Amphipsocidae and Caeciliusidae was not supported, although the causes of this were the placement of two distinct subfamilies (Paracaeciliinae and Calocaeciliinae). The monophyly of Asiopsocidae could not be tested because it was sampled only by one species. Based on these results and consideration of morphological characters, we propose a new classification for Caeciliusetae, recognizing six families: Amphipsocidae, Stenopsocidae, Dasydemellidae, Asiopsocidae, Paracaeciliidae and Caeciliusidae. We expect that this new classification will stabilize the higher‐level taxonomy of this group and help to identify groups in need of further work among these insects.     

Comparative and functional morphology of wing coupling structures in Trichoptera: Annulipalpia

Several orders of morphologically four‐winged insects have evolved mechanisms that enforce a union between the mesothoracic and metathoracic wings (forewings and hindwings) during the wing beat cycle. Such mechanisms result in a morphologically tetrapterous insect flying as if it were functionally dipterous, and these mechanisms have been described for several insect orders. The caddisfly suborders Annulipalpia and Integripalpia (Trichoptera) each have evolved a wing coupling apparatus, with at least three systems having evolved within the suborder Annulipalpia. The comparative and inferred functional morphology of the putative wing coupling mechanisms is described for the annulipalpian families Hydropsychidae (subfamilies Macronematinae and Hydropsychinae), Polycentropodidae and Ecnomidae, and a novel form‐functional complex putatively involved with at‐rest forewing‐forewing coupling is described for Hydropsychidae: Smicrideinae. It is proposed that the morphology of the wing coupling apparatuses of Hydropsychinae and Macronematinae are apomorphies for those clades. J. Morphol. 2009. © 2009 Wiley‐Liss, Inc.     

Does wing reduction influence the relationship between altitude and insect body size? A case study using New Zealand's diverse stonefly fauna

Researchers have long been intrigued by evolutionary processes that explain biological diversity. Numerous studies have reported strong associations between animal body size and altitude, but insect analyses have often yielded equivocal results. Here, we analyze a collection database of New Zealand's diverse endemic stonefly fauna (106 species across 21 genera) to test for relationships between altitude and plecopteran body size. This insect assemblage includes a variety of wing‐reduced (26 spp) and fully winged (80 spp) taxa and covers a broad range of altitudes (0–2,000 m). We detected significant relationships between altitude and body size for wing‐reduced, but not fully winged, stonefly taxa. These results suggest that, while the maintenance of flight apparatus might place a constraint on body size in some fully winged species, the loss of flight may free insects from this evolutionary constraint. We suggest that rapid switches in insect dispersal ability may facilitate rapid evolutionary shifts across a number of biological attributes and may explain the inconsistent results from previous macroecological analyses of insect assemblages.     

Comparing wing loading,flight muscle and lipid content in ant‐attended and non‐attended Tuberculatus aphid species

Although all Tuberculatus aphids possess wings, some species associated with ants exhibit extremely low levels of dispersal compared with those not associated with ants. Furthermore, phylogenetic interspecific comparisons find significantly higher wing loading (i.e. higher ratio of body volume to wing area) in ant‐attended species. This observation indicates that ant‐attended species may allocate more of their body resources to reproductive traits (i.e. embryos) rather than flight apparatus (i.e. wings, flight muscle and lipid). The present study focuses on two sympatric aphid species and aims to investigate the hypothesized trade‐off in resource investment between fecundity and the flight apparatus; specifically, the ant‐attended Tuberculatus quercicola (Matsumura) and non‐attended Tuberculatus paiki Hille Ris Lambers. Species differences are compared in: (i) morphology, (ii) embryo production, (iii) triacylglycerol levels and (iv) wing loading and flight muscle. The results show that T. quercicola has a larger body volume, higher fecundity and higher wing loading compared with T. paiki, which has a smaller, slender‐shaped body, lower fecundity and lower wing loading. No significant difference is found between the species with respect to the percentage of triacylglycerol content in dry body weight. The flight muscle development is significantly lower in T. quercicola than in T. paiki. These results indicate that the additive effect of higher wing loading and the lower amount of flight muscle development in T. quercicola may increase the physical difficulty of flight, and hence be responsible for its lower dispersal ability. The trade‐off between fecundity and dispersal documented in wing‐dimorphic insects may therefore be applicable to T. quercicola, which has fully developed wings.     

Physiological trade‐offs between flight muscle and reproductive development in the wing‐dimorphic cricket Velarifictorus ornatus

Morphology, flight muscles, and reproductive development were compared between long‐winged (LW) and short‐winged (SW) morphs of the cricket Velarifictorus ornatus (Shiraki) (Orthoptera: Gryllidae). There was no difference in body weight and pre‐oviposition between the two morphs, but LW individuals had better‐developed flight muscles than SW individuals during and after emergence of the adult. The flight muscles at adult emergence represented 11.9% of the total body weight in the LW female and 4.9% in the SW female. In addition, the weight of the flight muscle of LW females increased by 50% during the first 5 days, whereas the flight muscle of the SW variant increased only slightly after adult emergence. The process of oviposition in LW, SW, and de‐alated females varied: SW females produced more eggs at the early stage than LW females, but de‐alation could shorten the time until the peak of egg laying and caused histolysis of flight muscles of LW females. There was no significant difference in total egg production between the above three groups. In the male, unlike the female, the accessory glands of the two wing morphs enlarged continuously at the same rate. There was no difference between the two wing morphs in the mass of the testes during the first 7 days after adult emergence.     

Morph‐specific differences in biochemical composition related to flight capability in the wing‐polyphenic Sitobion avenae

Flight performance at various times after emergence in the alate morph and age‐dependent changes in biochemical composition of winged and wingless morphs were evaluated in the wing‐polyphenic aphid Sitobion avenae (Fabricius) (Hemiptera: Aphididae). Alates exhibited the highest flight activity at 18–36 h after adult emergence. Throughout the nymphal and adult development, the whole‐body content of total lipid was significantly higher in the winged vs. wingless morph, whereas the content of water, soluble sugar, glycogen, phospholipid, and soluble protein showed significantly higher levels in the wingless vs. winged morph. There were no significant differences in the content of triglyceride and free fatty acid during nymphal and adult stages in both morphs. However, triglyceride content was significantly higher in the winged vs. wingless morph during adulthood. Differences in biochemical composition between morphs indicate that there is an energetic cost of flight capability. Our results from S. avenae adults showed that total lipid and triglyceride for the winged morph accumulated significantly to a maximum, and water content decreased significantly to a minimum, on days 1 and 2 after the final molt, exactly when the highest flight activity was reached. This study suggests that flight activity is associated with triglyceride and water content.     

Morphology of male genitalia in lice and their relatives and phylogenetic implications

Abstract.  Lice (Insecta: Phthiraptera) have long been considered to compose a monophyletic group of insects on the basis of external morphological characteristics. However, a recent phylogenetic analysis of 18S rDNA sequences suggested that 'Phthiraptera' have arisen twice within the order Psocoptera (booklice and barklice). The external features of lice are highly specialized to a parasitic lifestyle, and convergence may be frequent for such characters. To provide a further test between traditional and recent molecular-based phylogenetic hypotheses, a phylogenetic analysis of lice and relatives based on morphological characters that are independent from the selective pressures of a parasitic lifestyle is needed. Here, we examined the morphology of the male phallic organ in lice and relatives ('Psocoptera': suborders Troctomorpha and Psocomorpha) and detected some novel modifications that were stable within each group and useful for higher level phylogenetic reconstruction. Phylogenetic analysis based on these characters provided a concordant result with the 18S-based phylogeny. In particular, the apomorphic presence of articulations between the basal plate, mesomere and ventral plate (= sclerite on the permanently everted endophallus) is observed consistently throughout the psocid families Pachytroctidae and Liposcelididae and the louse suborder Amblycera, providing support for a clade composed of these three groups, although possible homoplasy was detected in some Ischnocera. This is the first study to provide morphological support for the polyphyly of lice.     

Do insects lose flight before they lose their wings? Population genetic structure in subalpine stoneflies

Wing reduction and flightlessness are common features of alpine and subalpine insects, and are typically interpreted as evolutionary adaptations to increase fecundity and promote local recruitment. Here, we assess the impact of wing reduction on dispersal in stoneflies (Plecoptera: Gripopterygidae: Zelandoperla ) in southern New Zealand. Specifically, we present comparative phylogeographic analyses (COI; H3) of strong-flying Zelandoperla decorata (144 individuals, 63 localities) vs. the co-distributed but weak-flying Zelandoperla fenestrata species group (186 individuals, 81 localities). The latter group exhibits a variety of morphotypes, ranging from fully winged to completely wingless. Consistent with its capacity for strong flight-mediated dispersal, Z .  decorata exhibited no substantial phylogeographic differentiation across its broad South Island range. Conversely the weak-flying fenestrata species group exhibited substantial genetic structure across both fine and broad geographic scales. Intriguingly, the variable degrees of wing development observed within the fenestrata species group had no apparent impact on levels of phylogeographic structure, which were high regardless of morphotype, suggesting that even fully winged specimens of this group do not fly. This finding implies that Zelandoperla flight loss occurs independently of wing loss, and might reflect underlying flight muscle reduction.     

Molecular systematics of Psocomorpha (Psocoptera)

Abstract.  Previous classification of the insect order Psocoptera has relied on morphological characters. Psocoptera are generally divided into three suborders: Trogiomorpha, Troctomorpha, and Psocomorpha. Traditional classification divides the Psocomorpha into four infraorders (Homilopsocidea, Caeciliusetae, Psocetae and Epipsocetae), but a recent morphological cladistic study removed Archipsocidae from Homilopsocidea and Hemipsocidae from Psocetae. We investigated the phylogenetic relationships within the suborder Psocomorpha using DNA sequences from the nuclear 18S and mitochondrial 16S, 12S and cytochrome oxidase I genes. Phylogenetic analyses of these gene sequences supported monophyly for Psocomorpha. In addition, monophyly of the traditional subgroups Caeciliusetae and Psocetae was generally supported. Monophyly of Homilopsocidea was not supported, and Archipsocus is removed from this group. Although the molecular phylogeny is generally consistent with recent cladistic studies of morphological characters, we found no evidence that Hemipsocidae should be removed from Psocetae.     

Wing Dimorphisms and the Evolution of Migratory Polymorphisms among the Insecta

Many species of insects exhibit wing dimorphism, one morph havingfully developed wings and the other morph having reduced wingsand being incapable of flight. These wing dimorphisms providevisible manifestations of migratory polymorphisms. Since wingedindividuals do not, in principle, have to fly, the existenceof forms with reduced wings suggests that there is a tradeoffbetween flight capability and other fitness components. Comparisonsof the life histories of the fully winged and wing reduced morphsdemonstrate that this tradeoff is most commonly expressed asa decrease in the age of first reproduction and increased fecundityin the morph with reduced wings. Given these tradeoffs, theevolution of wing dimorphism will depend upon its genetic basis,including correlations with other life history components. Areview of the recent literature suggests that the heritabilityof wing morphology is high, and we suggest that this high heritabilitycould be maintained, in part, by antagonistic pleiotropy. In dimorphic species, the winged morph is generally consideredto be the migrant form. However, there are significant correlations,both within and among species, between the proportion of wingedindividuals, the proportion of winged individuals with functionalflight muscles, and the flight propensity of those individuals.This suggests that the proportion of winged individuals andthe propensity of the winged morph to migrate are intimatelyconnected at both the physiological and population level. Therefore,the study of the evolution of wing dimorphism is important notonly in its own right but also as a model of how migratory propensityevolves in monomorphically winged species.     

The trade‐off to macroptery in the cricket Gryllus firmus: a path analysis in males

Among the Orthoptera, wing dimorphism, where one morph is long‐winged and flight capable while the other is short‐winged and flight incapable, is common and believed to be maintained in populations due to trade‐offs to flight capability. In males, macropterous individuals call less than micropterous individuals and as a consequence obtain fewer matings. This trade‐off is hypothesized to be mediated by the energetic costs of calling. In this paper we report results for a path analysis examining lipid weight and DLM (dorso longitudinal muscle) condition of male Gryllus firmus. We found that as DLM condition changes from a nonfunctional to a functional state, call duration decreases, and as lipid weight increases, call duration increases. The most important linked path was wing morph → DLM condition → call duration. This model is consistent with the prediction that the trade‐off between wing morph and call duration is mediated via DLM and lipid stores.     

Wing dimorphism in the migratory locust,Locusta migratoria: differentiation of wing morph and phase polyphenism

A short‐winged morph was recently discovered in the migratory locust, Locusta migratoria. It is different from the normal, long‐winged morph not only in forewing length but also in hind femur length, displaying a dimorphism. To understand the significance of this dimorphism, other morphological characters were compared between the two morphs, and the time of differentiation of wing‐pad length was investigated. Wing weights were heavier in the long‐winged morph than in the short‐winged morph. This result showed that the short‐winged morph is not formed by a failure of wing expansion. No obvious morph‐specific differences were observed in wing venation, but wing allometry studies indicated that the distal areas of the fore‐ and hindwings were disproportionally reduced in the short‐winged morph compared to the long‐winged morph. The morphological differentiation of the wing pad between the two morphs was observed at the penultimate nymphal stage. The flight muscle was well developed in the two morphs, and no sign of flight muscle histolysis was detected in either morph after adult emergence. An analysis of adult body dimensions suggested that the density‐dependent phase shifts known for the long‐winged morph of this locust were also exhibited by the short‐winged morph, demonstrating that these shifts are not specific to the migratory long‐winged morph.     

Genome‐wide SNPs reveal fine‐scale differentiation among wingless alpine stonefly populations and introgression between winged and wingless forms

Insect flight loss is a repeated phenomenon in alpine habitats, where wing reduction is thought to enhance local recruitment and increase fecundity. One predicted consequence of flight loss is reduced dispersal ability, which should lead to population genetic differentiation and perhaps ultimately to speciation. Using a dataset of 15,123 SNP loci, we present comparative analyses of fine‐scale population structure in codistributed Zelandoperla stonefly species, across three parallel altitudinal transects in New Zealand's Rock and Pillar mountain range. We find that winged populations (altitude 200–500 m; Zelandoperla decorata) show no genetic structuring within or among streams, suggesting substantial dispersal mediated by flight. By contrast, wingless populations (Zelandoperla fenestrata; altitude 200–1100 m) exhibit distinct genetic clusters associated with each stream, and additional evidence of isolation by distance within streams. Our data support the hypothesis that wing‐loss can initiate diversification in alpine insect populations over small spatial scales. The often deep phylogenetic placement of lowland Z. fenestrata within their stream‐specific clades suggests the possibility of independent alpine colonization events for each stream. Additionally, the detection of winged, interspecific hybrid individuals raises the intriguing possibility that a previously flightless lineage could reacquire flight via introgression.     

Variation in singing behaviour among morphs of the sand field cricket,Gryllus firmus

1. Trade‐offs play a fundamental role in the evolution of many traits. 2. In wing‐polymorphic field crickets, the long‐winged morph can disperse from unfavourable environments, but has lower reproductive success than the short‐winged morph, because of costs associated with flight capability. 3. However, long‐winged individuals may minimise costs in favourable environments by histolysing their flight muscles and becoming flightless. 4. Few studies have examined how flight‐muscle histolysis affects male signalling and mate attraction. 5. We examined differences in singing activity and song characteristics among the flightless (short‐winged and histolysed long‐winged) and the flight‐capable male morphs, and female preferences for male song, in the sand field cricket. 6. We found: (i) both flightless morphs sang more than the flight‐capable morph, (ii) song characteristics varied among the three morphs, and (iii) females preferred songs characteristic of the long‐winged morphs. 7. Histolysis should increase mating success of long‐winged males because it increases singing activity. 8. Histolysed long‐winged males may have higher mating success than short‐winged males as they sing as frequently but produce more attractive songs. 9. Therefore, plasticity within the long‐winged morph may reduce costs of maturing in environments from which dispersal is not advantageous; non‐flying morphs may be pursuing different reproductive tactics.