Decision-making conditions for intra- or inter-nest mating of winged males in the male-dimorphic ant <Emphasis Type="Italic">Cardiocondyla minutior</Emphasis>

Only winged male and female ants generally mate through nuptial flight during the reproductive season. In the ants of Cardiocondyla, the males show wing dimorphism and their reproductive strategies differ depending on the differences in wing morphology. It has been suggested that wingless “ergatoid” males bearing very similar external morphologies to workers mate within natal nests, whereas winged males bearing typical ant male morphology disperse from their nests to mate. However, some behavioral observations suggest that the winged males of some Cardiocondyla ants such as C. obscurior and C. minutior may mate within natal nests before dispersion. We evaluated the factors affecting the mating behaviors of the winged males of C. minutior under laboratory conditions. We found that (1) the winged males remained and mated with virgin females in natal nests when either virgin winged females or the relatively mature pupae of winged females (i.e., at least 10 days) were present in the nest, (2) the winged males dispersed to adjacent nests with virgin winged females when only mated queens and the relatively young pupae of winged females (i.e., <9 days) were present in the nest, and (3) all winged males were accepted by the workers of non-natal nests irrespective of the distance from the natal nests in the field. Although most ergatoid males were accepted by the workers of close non-natal nests, they were all attacked and killed by the workers of distant non-natal nests. These results suggest that intra-nest mating and the dispersion of the winged males of C. minutior are facultatively determined by the condition of winged females (virginity and relative pupal age) in natal nests. Furthermore, our results suggest that winged males are likely to seek mating partners chemically and to mate with virgin winged females.     

Identification of acoustic stimuli that mediate sexual behavior inDrosophila busckii (Diptera: Drosophilidae)

We have shown that D. busckiimales and females, unlike other drosophilids that have been analyzed in this regard, court and copulate as well in relatively dim red light as they do in bright white light. We have also shown that males and females of this species flutter their wings during courtship and that wing fluttering in both sexes is associated with acoustic stimuli. Wingless males perform vigorous courtship but are incapable of mating, suggesting that females must perceive male song to be receptive to copulation. When they are tested with normal males, wingless females stimulate vigorous courtship, but their copulation frequencies are significantly lower than winged females. This observation suggests that perception of the female's song by either or both sexes facilitates mating.     

Alternative mating tactics and extreme male dimorphism in fig wasps

The dimorphisms in morphology and behaviour of male fig wasps are among the most extreme in the animal kingdom, and offer excellent opportunities to test the predictions of certain sexual selection models. Winged males resemble their conspecific females closely, but wingless males are so divergent in form that they have repeatedly been classified into different taxa. Wingless males mate within their natal fig fruits, whereas winged males disperse to mate. Individual species may have winged males, wingless males or both morphs. A key hypothesis proposes that sexual selection on male mating opportunities favours winged males in species with small broods and wingless males in species with large broods. Using data from 114 species in 33 genera, we show that both simple and formal comparative analyses support the correlated evolution of large brood size and male winglessness. Theoretical models further predict that, in male dimorphic species, the proportion of winged males should equal (in cases without local mate competition) or exceed (in cases with local mate competition) the proportion of females developing in fig fruits without wingless males. These predictions are met by eight out of nine male dimorphic species studied. Taken together, the patterns across all species, and between different male dimorphic species, strongly support sexual selection on mating opportunities as the major determinant of male morph ratios in fig wasps.     

Live and let die: why fighter males of the ant Cardiocondyla kill each other but tolerate their winged rivals

Unlike most social insects, many Cardiocondyla ant species havetwo male morphs: wingless (ergatoid) males, who remain in thenatal nest, and winged males who disperse but, strangely, beforeleaving may also mate within the nest. Whereas ergatoid malesare highly intolerant of each other and fight among themselves,they tend to tolerate their winged counterparts. This is despitethe fact that these winged males, like ergatoid males, representmating competition. Why should ergatoid males tolerate theirwinged rivals? We developed a mathematical model to addressthis question. Our model focuses on a number of factors likelytoinfluence whether ergatoid males are tolerant of winged males:ergatoid male–winged male relatedness, number of virginqueens, number of winged males, and the number of ejaculatesa winged male has (winged males are sperm limited, whereas ergatoidmales have lifelong spermatogenesis). Surprisingly, we foundthat increasing the number of virgin queens favors a kill strategy,whereas an increase in the other factors favors a let-live strategy;these predictions appear true for C. obscurior and for a numberof other Cardiocondyla species. Two further aspects, unequalinsemination success and multiple mating in queens, were alsoincorporated into the model and predictions made about theireffects on toleration of winged males. The model is applicablemore generally in species that have dimorphic males, such assome other ants, bees, and fig wasps.     

THE EVOLUTION OF ALTERNATIVE REPRODUCTIVE TACTICS IN MALE CARDIOCONDYLA ANTS

Alternative reproductive tactics are often associated with discontinuous variation in morphology but may evolve independent from each other. Based on life‐history data and a phylogeny we examine how male morphology and reproductive behavior are linked in the evolution of the ant genus Cardiocondyla. Wingless Cardiocondyla males engage in lethal fighting for access to female sexuals, whereas winged males disperse and mate away from the nest. This basic pattern shows considerable variation across species. A phylogeny based on ～3 kbp sequence data shows that male diphenism and lethal fighting are ancestral traits tightly linked in evolution. Winged males were lost convergently in several species groups, apparently in response to the low probability of encountering female sexuals in nests without a resident fighter male. An early dichotomy separates two clades with alternative male morphologies and fighting behavior, but phenotype and fighting strategy are not correlated with the presence of winged males.     

Additions To The Flora Of Shetland

ABSTRACT

Background: Pallenis spinosa (Asteraceae) produces both winged and wingless achenes. Both achene morphs are non-dormant and show a similar embryo size, rendering dispersal ability as their only apparent functional difference.

Aims: We studied morph-specific release and spatial dispersal patterns to ascertain whether the common view of seed dimorphism as a mixed strategy, that is functionally fully differentiated morphs, is appropriate for this system.

Methods: For three years, at the onset of achene release, in early autumn, we placed achene traps at different distances from source plants, censusing achene arrival at 3–4 day intervals. We constructed morph-specific dispersal kernels and related release intensity to prevailing meteorological conditions in census intervals. Selected kernel models were used to describe dispersal effects of observed changes in the proportion of winged achenes (p_w) in successive released fractions.

Results: Achene release extended up to early-mid winter, peaking in rainy, windy intervals. Throughout the season, p_w decreased progressively. Unexpectedly, the wingless morph produced the longest dispersal tails and it only showed ability for fat-tailed dispersal. Consequently, maximum dispersal distances steadily increased throughout the season.

Conclusions: Achene dimorphism in P. spinosa appears to allow a within-season continuous reshaping of the seed-dispersal kernel instead of representing a mixed strategy.     

Die genetische Grundlage der Monogenie bei der Schmei?fliege Chrysomya rufifacies (Calliphoridae, Diptera)

Summary Recently in our wild stock of the monogenic blowfly Chrysomya rufifacies a recessive mutation white (w) causing white instead of red-brown eyes spontaneously appeared (Fig. 1). This marker gene enabled us to clarify the genetic basis of monogeny in this species. F₁ offspring produced by reciprocal crossings between normal (+/+) and white-eyed (w/w) flies were phenotypically wildtype (Table 1). In F₂ offspring of female-producing (thelygenic) and male-producing (arrhenogenic) F₁ females wildtype and white-eyed flies appeared in the expected 3:1 ratio; in several crossings a slight deviation of this ratio indicated a reduced viability of the w/w individuals (Table 2). Examination of F₂ progeny of thelygenic F₁+/w females, which had received the w allele from their father, showed that most of the F₂+/+ females were thelygenic, whereas most of the F₂ w/w females were arrhenogenic; among F₂+/w females thelygenic and arrhenogenic individuals occurred in almost equal numbers (Table 3). On the other hand, when F₂ offspring of thelygenic F₁+/w females which had inherited the w allele from their mother were tested, most of the F₂+/+ females turned out to be arrhenogenic and most of the F₂ w/w females thelygenic; among F₂+/w females thelygenic and arrhenogenic flies also were found in almost equal frequencies (Table 4). the sex-linked inheritance of the factor w following from these results was also confirmed by an analysis of the progeny of thelygenic F₁+/w females backcrossed with w/w males. Among the R₁ offspring of F₁+/w females, which had received the w allele from their father, the +/w females were predominantly thelygenic compared to their predominantly arrhenogenic w/w sisters (Table 5). Analysis of R₁ progeny of F₁+/w females, which had inherited the w allele from their mother, yielded reciprocal results (Table 6).This mode of incomplete sex-linkage of the mutation white observed in C. rufifacies (Figs. 2–5) supports the hypothesis that thelygenic females are heterozygous for a dominant female sex realizer (F') with predetermined sex-determining properties, and that arrhenogenic females as well as the males are homozygous for the recessive allele f (Fig. 6). The recombination frequency between F'/f and the w-Locus was calculated to be 12.72±0.72 per cent.

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Mit Unterstützung durch die Deutsche forschungsgemeinschaft.     

A new type of male dimorphism with ergatoid and short-winged males in Cardiocondyla cf. kagutsuchi

Summary. A new type of ant male dimorphism, consisting of wingless (ergatoid) and short-winged (brachypterous) males, was found in a species of the “Cardiocondyla kagutsuchi”- complex from Malaysia. The ergatoid males show the typical morphological and behavioral characteristics of those of many other Cardiocondyla species. The brachypterous males are morphologically intermediate between ergatoid males and typical winged males of other taxa in this genus. On one hand, they share a number of morphological and behavioral features with ergatoid males that might be adaptations to the loss of flight and intranidal mating: aggressive behavior towards rival males, a prolonged spermatogenesis, which is unique in winged males, paler body coloration, smaller compound eyes, shorter antennal funiculi, more rounded heads – perhaps due to the increased development of mandibular muscles, and an angular pronotum, probably for neck protection. Their short wings appear to protect the petiolar joints during fighting. On the other hand, the brachypterous males have not become as specialized as the ergatoids and to some extent keep the nature of the winged males of other species, i.e., they escape from the nest with a higher probability and with less injuries and do not show a reduction of the ocelli. In the sexual production season, the ergatoid males emerged first in small numbers and then both male morphs emerged in large numbers. The sex ratio was extremely female-biased in the earlier stage of sexual production, probably due to local mate competition.Received 13 December 2004; revised 17 February 2005; accepted 22 February 2005.     

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.     

Older triploid fish retain impaired reproductive endocrinology in the European sea bass Dicentrarchus labrax

This paper reports on an evaluation of growth, gonadal development and reproductive endocrinology of older triploid (3n) European sea bass Dicentrarchus labrax in comparison with their diploid (2n) counterparts throughout their fifth and seventh annual cycle of life. While older triploids retained impaired reproductive endocrinology, a sexually related dimorphic growth was observed with 3n females attaining the largest sizes. Comparisons of some body indexes showed that 3n females had a significantly lower hepato‐somatic index (I_H) than 2n females but a significantly higher viscero‐somatic index (I_F). In contrast, both male and female triploids showed significantly lower gonado‐somatic index (I_G) than diploids. Accordingly, diploids produced mature gametes but triploids did not, demonstrating that despite the longer time given to triploids for gonadal development, they could not reproduce. Furthermore, older triploids had lower levels of plasma sex steroids (testosterone, T; 11‐ketotestosterone, 11‐KT and oestradiol‐17β, E₂) and luteinizing hormone (LH) than their 2n counterparts with 3n females showing drastic effects of triploidization on their reproductive endocrinology. Vitellogenin (VTG) was undetectable in 3n females. Gonadal content of steroid hormones and Sparus aurata‐type gonadotropin‐releasing hormone (sbGnRH) in the brain and pituitary were also lower in triploids compared with diploids. These results suggest that older 3n D. labrax retain functional sterility in both sexes, and 3n females might reach larger sizes than 3n males and their 2n counterparts in this species.     

Photoperiodic determination of gynoparae and males of damson-hop aphid Phorodon humuli

Abstract. Sexual morph production in Phorodon humuli is controlled by daylength. Wingless aphids reared from birth in short-day conditions (LD 12 : 12 h) and transferred when adult to long-day conditions (LD 18 : 6 h) produce only gynoparae and males until death some 7 weeks later, whereas those reared in long days and transferred to short days produce 20% wingless parthenogenetic females, 50% gynoparae and 30% of males in an overlapping sequence. No winged morph capable of re-infesting hop is produced. Less mature embryos are more sensitive to short days than older embryos because 100% of the former became gynoparae after 4 days of exposure of their mothers, and 59% when their mothers were exposed for the 4 days immediately preceding the birth of their offspring. Two days of exposure to short days switches 94% of young embryos from wingless to gynopara production when mature. The response to short days is irreversible. Wingless aphids reared from birth to adult in short days produce 30% fewer offspring than those reared to the same stage in long days and are male-biased, with 76–78% of their offspring being male.     

Genetic variation for sexual dimorphism in flower size within and between populations of gynodioecious Thymus vulgaris

There has been very little empirical study of quantitative genetic variation in flower size in sexually dimorphic plant species, despite the frequent occurrence of flower size differences between sexual phenotypes. In this study we quantify the nature of quantitative flower size variation in females and hermaphrodites of gynodioecious Thymus vulgaris. In a field study, females had significantly smaller flowers than hermaphrodites, and the degree of flower size dimorphism varied significantly among populations. To quantify the genetic basis of flower size variation we sampled maternal progeny from 10 F₀ females in three populations (across the range of variation in flower size in the field), performed controlled crosses on F₁ offspring in the glasshouse and grew F₂ progeny to flowering in uniform field conditions. A significant population * sex interaction was again observed, hence the degree of sexual dimorphism shows genetic variation among populations. A significant family * sex interaction was also observed, indicating that the degree of sexual dimorphism shows genetic variation among families. Females showed significantly greater variation among populations and among families than hermaphrodites. Female flower size varied significantly depending on the degree of stamen abortion, with morphologically intermediate females having flowers more similar to hermaphrodites than to other females. The frequency of female types that differ in the degree of stamen abortion varied among populations and families and mean family female flower size increased as the proportion of intermediate female types increased across families. Variation in the degree of flower size dimorphism thus appears to be a result of variation in the degree of stamen abortion in females, the potential causes of which are discussed.     

Photosynthesis performance in sweet almond [<Emphasis Type="Italic">Prunus dulcis</Emphasis> (Mill) D. Webb] exposed to supplemental UV-B radiation

Due to anthropogenic influences, solar UV-B irradiance at the earth’s surface is increasing. To determine the effects of enhanced UV-B radiation on photosynthetic characteristics of Prunus dulcis, two-year-old seedlings of the species were submitted to four levels of UV-B stress, namely 0 (UV-B_c), 4.42 (UV-B₁), 7.32 (UV-B₂) and 9.36 (UV-B₃) kJ m⁻² d⁻¹. Effects of UV-B stress on a range of chlorophyll (Chl) fluorescence parameters (FPs), Chl contents and photosynthetic gas-exchange parameters were investigated. UV-B stress promoted an increase in minimal fluorescence of dark-adapted state (F₀) and F₀/F_m, and a decrease in variable fluorescence (F_v, F_v/F_m, F_v/F₀ and F₀/F_m) due to its adverse effects on photosystem II (PSII) activity. No significant change was observed for maximal fluorescence of dark-adapted state (F_m). Enhanced UV-B radiation caused a significant inhibition of net photosynthetic rate (P _N) at UV-B₂ and UV-B₃ levels and this was accompanied by a reduction in stomatal conductance (g _s) and transpiration rate (E). The contents of Chl a, b, and total Chl content (a+b) were also significantly reduced at increased UV-B stress. In general, adverse UV-B effects became significant at the highest tested radiation dose 9.36 kJ m⁻² d⁻¹. The most sensitive indicators for UV-B stress were F_v/F₀, Chl a content and P _N. Significant P<0.05 alteration in these parameters was found indicating the drastic effect of UV-B radiation on P. dulcis.     

Wingless and intermorphic males in the ant <Emphasis Type="Italic">Cardiocondyla venustula</Emphasis>

The ant genus Cardiocondyla is characterized by a pronounced male diphenism with wingless fighter males and winged disperser males. Winged males have been lost convergently in at least two species-rich clades. Here, we describe the morphological variability of males of Cardiocondyla venustula from uThukela valley, South Africa. Winged males appear to be absent from this species. However, in addition to wingless (“ergatoid”) males with widely fused thoracic sutures and without ocelli, “intermorphic” males exist that combine the typical morphology of wingless males with characteristics of winged males, e.g., more pronounced thoracic sutures, rudimentary ocelli, and vestigial wings. Similar “intermorphic” males have previously been described from one of several genetically distinct lineages of the Southeast Asian “Cardiocondyla kagutsuchi” complex (Insect. Soc. 52: 274-281, 2005). To determine whether male morphology is associated with distinct clades also in C. venustula, we sequenced a 631 bp fragment of mitochondrial DNA of workers from 13 colonies. We found six haplotypes with a sequence variation of up to 5.7 %. Intermorphic and wingless males did not appear to be associated with a particular of these lineages and within colonies showed the same sequence. Interestingly, two colonies contained workers with different haplotypes, suggesting the occasional migration of queens and/or workers between colonies.     

Morphological and histological examination of short‐wing formation in the winter moth Protalcis concinnata (Insecta: Lepidoptera,Geometridae)

Winter geometrid moths exhibit sexual dimorphism in wing length and female‐specific flightlessness. Female‐specific flightlessness in insects is an interesting phenomenon in terms of sexual dimorphism and reproductive biology. In the winter geometrid moth, Protalcis concinnata (Wileman), adult females have short wings and adult males have fully developed wings. Although the developmental process for wing reduction in Lepidoptera is well studied, little is known about the morphology and the developmental pattern of short‐winged flightless morphs in Lepidoptera. To clarify the precise mechanisms and developmental processes that produce short‐winged morphs, we performed morphological and histological investigations of adult and pupal wing development in the winter geometrid moth P. concinnata. Our findings showed that (a) wing development in both sexes is similar until larval‐pupal metamorphosis, (b) the shape of the sexually dimorphic wings is determined by the position of the bordering lacuna (BL), (c) the BL is positioned farther inward in females than in males, and (d) after the short pupal diapause period, the female pupal wing epithelium degenerates to approximately two‐thirds its original size due to cell death. We propose that this developmental pattern is a previously unrecognized process among flightless Lepidoptera.     

Response of photosynthesis and chlorophyll fluorescence quenching to leaf dichotocarpism in Ligustrum vicaryi, an ornamental herb

Net photosynthetic rate of yellow upper leaves (UL) of Ligustrum vicaryi was slightly, but not significantly higher than that of green lower leaves (LL). Diurnally, maximum photochemical efficiency of photosystem 2, PS2 (F_v/F_m) of LL did not significantly decline but the UL showed fairly great daily variations. Yield of PS2 of UL showed an enantiomorphous variation to the photosynthetically active radiation and was significantly lower than in the LL. Unlike F_v/F_m, the efficiency of energy conversion in PS2 and both non-photosynthetic and photosynthetic quenching did not differ in UL and LL. Significant differences between UL and LL were found in contents of chlorophyll (Chl) a, b, and carotenoids (Car) and ratios of Chl a/b, Chl b/Chl (a+b), and Car/Chl (a+b). Leaf colour dichotocarpism in L. vicaryi was mainly caused by different photon utilization; sunflecks affected the LL.     

Reproductive strategies of two forms of flightless males in a non‐pollinating fig wasp under partial local mate competition

1. The underlying basis of alternative male reproductive strategies is either genetic or environmental. Several non‐pollinating fig wasp lineages have dimorphic males, typically with winged males that disperse from natal figs to mate and flightless males that seek mating opportunities in natal figs. 2. Walkerella sp. from Ficus benjamina has dark and pale wingless males. Observations and experiments in Xishuangbanna, Southern China found that (i) the sex ratio of Walkerella sp. did not vary with foundress number or brood size. (ii) The frequency of dark males increased with brood size and foundress number and they were absent from figs with a single foundress. This produced a higher proportion of dark males at higher densities. (iii) Males of both morphs fought, but injuries to dark males were more frequent. (iv) Dark males were more likely to disperse away from their natal figs and (v) they were more resistant to dehydration. 3. Responses to selection are constrained by the genetic options available. Consequently, selection pressures acting on different lineages can produce similar outcomes that are achieved in different ways. Walkerella species lack winged males, but dark males display some of their features, dispersing from natal figs and displaying appropriate physiological and behavioural adaptations. However, dark males also displayed increased levels of damage from fighting – a feature unlikely to be shared with the winged males of other species.     

Mate guarding and alternative reproductive tactics in the ant Hypoponera opacior

In many animals, males have evolved weapons, elaborate courtship displays, or costly ornaments to increase their reproductive success. Ants, in contrast, commonly mate during nuptial flights, in which males do not profit from fighting or attempting to monopolize females. However, where mating occurs in the nest, males can use other reproductive tactics. We found that wingless (apterous) males of Hypoponera opacior sat on top of queen cocoons, inserted their genitalia into the cocoons and remained in copula with cocooned queens for up to 40 h. These males were tolerant of each other; fighting was never recorded. Our observations therefore suggest that wingless males of H. opacior ensure reproduction by copulatory mate guarding. This strategy, although time consuming, presumably reduces the likelihood of subsequent inseminations by other males. Apterous H. opacior males have only a limited amount of sperm available: histological preparations showed that, in contrast to Cardiocondyla fighter males, the testes degenerate in early adult life. Males ofH. opacior have relatively few mating opportunities. Although some wingless males were reproductively active for more than 3 weeks, we observed a maximum of only six matings per male, with a mean slightly above one. SomeH. opacior males used an alternative reproductive tactic of dispersal and outbreeding. We found colonies headed by single, dealate queens, which did not rear wingless sexuals but presumably reproduced through winged reproductives that mate in nuptial flights. The social structure of those colonies contrasted with nests containing wingless reproductives, which were highly polygynous and polydomous.     

Ontogenetic scaling of the human nose in a longitudinal sample: Implications for genus Homo facial evolution

Researchers have hypothesized that nasal morphology, both in archaic Homo and in recent humans, is influenced by body mass and associated oxygen consumption demands required for tissue maintenance. Similarly, recent studies of the adult human nasal region have documented key differences in nasal form between males and females that are potentially linked to sexual dimorphism in body size, composition, and energetics. To better understand this potential developmental and functional dynamic, we first assessed sexual dimorphism in the nasal cavity in recent humans to determine when during ontogeny male‐female differences in nasal cavity size appear. Next, we assessed whether there are significant differences in nasal/body size scaling relationships in males and females during ontogeny. Using a mixed longitudinal sample we collected cephalometric and anthropometric measurements from n = 20 males and n = 18 females from 3.0 to 20.0+ years of age totaling n = 290 observations. We found that males and females exhibit similar nasal size values early in ontogeny and that sexual dimorphism in nasal size appears during adolescence. Moreover, when scaled to body size, males exhibit greater positive allometry in nasal size compared to females. This differs from patterns of sexual dimorphism in overall facial size, which are already present in our earliest age groups. Sexually dimorphic differences in nasal development and scaling mirror patterns of ontogenetic variation in variables associated with oxygen consumption and tissue maintenance. This underscores the importance of considering broader systemic factors in craniofacial development and may have important implications for the study of patters craniofacial evolution in the genus Homo. Am J Phys Anthropol 153:52–60, 2014. © 2013 Wiley Periodicals, Inc.     

Polymorphic fundatrices in thimbleberry aphid — ecology and maintenance

The thimbleberry aphid,Masonaphis maxima (Mason) lives on patches of plants that support 3,4 or 5 generations depending on site and weather. The life cycle requires sexual females and males to produce overwintering eggs. The eggs hatch in the spring to produce the first ’fundatrix’ generation; subsequent generations are produced parthenogenically. Males and other morphs are produced by wingless virginoparae, but sexual females are produced by ’gynoparae’, a winged morph that is specialized to produce only sexual females. The fundatrices have no indication of the number of generations that the plants will support in the current year. There are two fundatrix types that coexist in different ratios depending on the number of generations supported by the patch the previous year. One type produces sexual females in generations 3 and 5, and males in generations 4 and 5; the other type produces sexual females in generations 4 and 5, and males in generations 3, 4 and 5. The dimorphism adapts the aphid to its heterogeneous and somewhat unpredictable environment. The role of sex in the maintenance of the dimorphism is discussed. This is the first report of fundatrix polymorphism and consequent differential sex expression in aphids.