GENETICS OF GRACILARIA TIKVAHIAE (RHODOPHYCEAE). X. STUDIES ON A BISEXUAL CLONE12

A male done of the red alga Gracilaria tikvahiae McLachlan spontaneously produced a bisexual frond which remained bisexual in subsequent subcultures. Both male and female components of bisexual fronds were functional; however, some unusual results were obtained in crosses. When bisexual fronds were crossed with a normal haploid male, the resulting carpospores all developed into diploid male gametophytes. When bisexual plants were self fertilized, all the carpospores yielded diploid bisexual gametophytes. Only when bisexual plants were crossed to normal haploid females, did carpospores develop into diploid tetrasporophytes as they normally do. The F₁ gametophyte generation obtained from these tetrasporophytes, however, included not only females and males but also bisexual plants, in a 2:1:1 ratio. These results are consistent with the interpretation that bisexual plants have a recessive mutation of a gene other than the primary sex determining locus, and that this mutation is expressed only in male plants. It is suggested that the altered gene may ordinarily have a regulatory function in the maintenance of the dioecious condition.     

The effect of interspecific mating on sex ratios in the twospotted spider mite and the Banks grass mite (Acarina: Tetranychidae)

Mixed populations of the twospotted spider mite (TSM),Tetranychus urticae (Koch), and the Banks grass mite (BGM),Oligonychus pratensis (Banks), occur on corn and sorghum plants in late summer in the Great Plains. Interspecific matings between these arrhenotokous species occur readily in the laboratory but yield no female offspring. The effect of interspecific mating on female: male sex ratios was measured by examining the F₁ progeny of females that mated with both heterospecific and conspecific males in no-choice situations. TSM females that mated first with BGM males and then with TSM males produced a smaller percentage of female offspring than TSM females that mated only with TSM males (43.1±5.8 and 78.9±2.8% females, respectively). Similarly, BGM females mated with heterospecific males and then with conspecific males produced fewer female offspring than females mated only with BGM males (55.7±5.2 and 77.5±2.5%, respectively). Lower female: male sex ratios were produced also by BGM females that mated with TSM males after first mating with conspecifics (62.4±3.4%). In mixed populations containing males of both species, females also produced lower female: male sex ratios, but these ratios were not as low as expected based on mating propensities and progeny sex ratios observed in no-choice tests. These data suggest that interspecific mating may substantially reduce female fitness in both mite species by reducing the output of female offspring, but in mixed populations this effect is mitigated by unidentified behavioral mechanisms.     

Unexpectedly low frequencies of diploid males in an inbreeding parasitoid with complementary sex determination

In hymenopterans with single locus complementary sex determination, sex depends on the genotype at one polymorphic locus. Haploids are always male, while diploids are female when heterozygous and male when homozygous at the sex‐determining locus. Brothers and sisters have a 50% chance of sharing a sex allele (i.e. of being ‘matched’), and hence half of all sibling matings are expected to produce diploid males at the expense of females. Nevertheless, observed frequencies of diploid males are often lower than predicted, as diploid males may succumb to pre‐imaginal mortality, or because unmatched mates or sperm enjoy a competitive advantage. We counted diploid males in broods of the parasitoid wasp Cotesia glomerata sampled in the field, and in broods produced through controlled laboratory crosses. Consistently, the frequency of diploid males fell below expectations based upon the estimated occurrence of sibling mating. In the staged broods with diploid males, females made up a disproportionately large share of the diploids. Broods with and without diploid males were of similar size. Hence, the shortage of diploid males cannot be accounted for by differential pre‐imaginal mortality alone. Instead, we postulate the existence of a mechanism that leads to preferential fertilization of eggs by sperm bearing unmatched alleles. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ●● , ●●–●●.     

Sex-linked control of sex pheromone behavioral responses in European corn-borer moths (Ostrinia nubilalis) confirmed with TPI marker gene

In two races of European corn-borer moths (ECB), the E-race females emit and males respond to 99:1 sex pheromone blend of (E)/(Z)-11-tetradecenyl acetates, whereas the Z-race females and males produce and respond to the opposite 3:97 pheromone blend of (E)/(Z)-11-tetradecenyl acetates, respectively. We previously have shown that female production of the final blend ratio is under control of a major autosomal locus but that the sequence of male upwind flight responses to the blend is controlled by a sex-linked (Z-linked) locus. This sex-linked control of behavioral responses in crosses of E and Z ECB now is confirmed by use of sex-linked TPI (triose phosphate isomerase) allozyme phenotypes to determine the origin of the sex chromosomes in F₂ populations. F₁ males from reciprocal E × Z crosses generate similar behavioral-response profiles in wind-tunnel studies, with moderate numbers responding to the Z pheromone and intermediate blends (35%–65% Z), but very few responding to the E pheromone. The F₂ behavioral-response profiles indicate that they are composed of 1:1 mixtures of hybrids and paternal profiles. Analysis of TPI allozyme differences allowed us to separate male F₂ populations into individuals whose Z chromosomes both originated from their grandfathers, and individuals who had one Z chromosome originating from each grandparent. With these partitioned F₂s, the TPI homozygotes exhibited behavioral-response profiles very much like their grandfathers, whereas the TPI hybrids produced response profiles similar to their heterozygous F₁ fathers. These results demonstrate incontrovertibly that the response to sex pheromone in male ECB is controlled by a sex-linked gene that is tightly linked to the TPI locus and therefore is independent of the locus controlling pheromone blend production in females.     

Spontaneous polyploidy,gynogenesis and androgenesis in second generation (F2) koi Cyprinus carpio × goldfish Carassius auratus hybrids

The objective of this study was to characterize the genetics of second generation (F₂) koi Cyprinus carpio × goldfish Carassius auratus hybrids. Spermatozoa produced by a novel, fertile F₁ male were found to be diploid by flow‐cytometric analysis. Backcross (F₁ female × C. carpio male and C. carpio female × F₁ male) juveniles were triploid, confirming that female and male F₁ hybrids both produced diploid gametes. The vast majority of surviving F₂ juveniles was diploid and small proportions were aneuploid (2·1n–2·3n and 3·1n–3·9n), triploid (3n) and tetraploid (4n). Microsatellite genotyping showed that F₂ diploids repeated either the complete maternal or the complete paternal genotype. Fish with the maternal genotype were female and fish with the paternal genotype were male. This demonstrates that F₂ diploids were the result of spontaneous gynogenesis and spontaneous androgenesis. Analysis of microsatellite inheritance and the sex ratio in F₂ crosses showed that spontaneous gynogenesis and androgenesis did not always occur in equal proportions. One cross was found to have an approximate equal number of androgenetic and gynogenetic offspring while in several other crosses spontaneous androgenesis was found to occur more frequently than spontaneous gynogenesis.     

Effect of mating combinations on the host parasitisation and sex allocation in solitary endoparasitoid,Aenasius arizonensis (Hymenoptera: Encyrtidae)

Aenasius arizonensis (Girault) is an important solitary endoparasitoid of Phenacoccus solenopsis Tinsley. To optimise the mass production of high-quality females, it is important to assess the influence of mating regimes on the progeny fitness and sex allocation. We, therefore, hypothesise that mating combinations in A. arizonensis adults emerged from different host instars may influence parasitism and sex allocation in the subsequent generation. Therefore, we compared three nymphal instars (1st, 2nd and 3rd) and adults host stages of P. solenopsis for parasitism and sex allocation by A. arizonensis. Further, F₁ female progeny of the parasitoid emerged from different host instars was henceforth evaluated for its fitness in six mating combinations. A. arizonensis females parasitised all the host stages except the 1st instar nymphs. The parasitised 2nd instar nymphs yielded only males, while the sex ratio in the later host instars was strongly female-biased. The parasitoid females preferred 3rd instar nymphs with respect to higher parasitism (74.0–84.0%) and produced more females in the F₁ progeny as compared to other host stages. F₁ females that emerged from 3rd instar nymphs produced significantly higher parasitism (74.0–79.0%). These mating combinations also yielded more female progeny in the F₂ generation. However, parasitism by F₁ females was significantly lower (9.0–12.0%) when mated with males that emerged from 2nd instar P. solenopsis nymphs. Moreover, latter combinations yielded only male progeny in F₂ generation. These findings can be used in laboratory mass rearing of this parasitoid vis-à-vis biological control of P. solenopsis.     

Triploid females and diploid males: underreported phenomena in <Emphasis Type="Italic">Polistes</Emphasis> wasps?

Summary In hymenopteran species, males are usually haploid and females diploid. However, in species that have complementary sex determination (CSD), diploid males arise when a female produces offspring that are homozygous at the sex-determining locus. Although diploid males are often sterile, in some species they have been shown to produce diploid sperm, thus producing triploid daughters if they mate successfully. Diploid males have been observed in very few species of social wasps, and we know of no published reports of triploid females. In this paper, we review the existing literature on diploid males and triploid females in the Hymenoptera, and report the observation of triploid females in three species of Polistes paper wasps. Although polyploid offspring may be produced parthenogenetically, the more likely scenario is that Polistes wasps have CSD and produce diploid males via homozygosity at the sex-determining locus. Therefore, female triploidy indicates that diploid males do exist in Polistes species where they are presumed to be absent, and are likely to be even more frequent among species that have experienced a genetic bottleneck. We conclude by cautioning against the assumption of a selective advantage to the production of early males, and by discussing the implications of male diploidy and female triploidy for measurement of sex ratio investment and assumptions of reproductive skew theory.Received 5 December 2003; revised 20 March 2004; accepted 19 April 2004.     

Elimination of Wolbachia from Urolepis rufipes (Hymenoptera: Pteromalidae) with Heat and Antibiotic Treatments: Implications for Host Reproduction

Molecular analyses using ftsZ and wsp primers identified infections of type-A Wolbachia bacteria in populations of Urolepis rufipes (Ashmead) (Hymenoptera: Pteromalidae), a potential biocontrol agent for pest flies (Diptera: Muscidae) in livestock confinements. Incidence of infections ranged from 10 to 45% for three field populations and 100% in a laboratory colony. Provision of adult wasps with sugar water containing 50 μg mL^–1 tetracycline hydrochloride, or continuous rearing at 34±0.5°C eliminated Wolbachia from experimental populations after four and six generations, respectively. Results were similar for experimental crosses between infected parents, between uninfected parents, and between infected female and uninfected male parents. Embryonic mortality was less than 5% for the F₁ generation, which had an adult sex ratio of 2♀:1♂. In contrast, experimental crosses between uninfected female and infected male parents were associated with an embryonic mortality of about 20% and produced 37% fewer F₁ adults. However, because of an F₁ sex ratio of almost 0♀:1♂,?this latter cross produced an overall higher number of F₁ males. These combined results reflect elements of both male development (MD) type cytoplasmic incompatibility (CI) and female mortality (FM) type CI Wolbachia. MD type CI Wolbachia in incompatible crosses causes haploidization of fertilized (i.e., female) eggs. The resultant haploid eggs develop into males so that more males are produced in incompatible versus compatible crosses. FM type CI produces fewer offspring and a male-biased F₁ generation caused by enhanced mortality of female embryos. We speculate that the fate of fertilized eggs - haploidization versus mortality - may reflect differences in bacterial densities.     

Geographic variation in sex‐chromosome differentiation in the common frog (Rana temporaria)

In sharp contrast with birds and mammals, sex‐determination systems in ectothermic vertebrates are often highly dynamic and sometimes multifactorial. Both environmental and genetic effects have been documented in common frogs (Rana temporaria). One genetic linkage group, mapping to the largest pair of chromosomes and harbouring the candidate sex‐determining gene Dmrt1, associates with sex in several populations throughout Europe, but association varies both within and among populations. Here, we show that sex association at this linkage group differs among populations along a 1500‐km transect across Sweden. Genetic differentiation between sexes is strongest (F_ST = 0.152) in a northern‐boreal population, where male‐specific alleles and heterozygote excesses (F_IS = ?0.418 in males, +0.025 in females) testify to a male‐heterogametic system and lack of X‐Y recombination. In the southernmost population (nemoral climate), in contrast, sexes share the same alleles at the same frequencies (F_ST = 0.007 between sexes), suggesting unrestricted recombination. Other populations show intermediate levels of sex differentiation, with males falling in two categories: some cluster with females, while others display male‐specific Y haplotypes. This polymorphism may result from differences between populations in the patterns of X‐Y recombination, co‐option of an alternative sex‐chromosome pair, or a mixed sex‐determination system where maleness is controlled either by genes or by environment depending on populations or families. We propose approaches to test among these alternative models, to disentangle the effects of climate and phylogeography on the latitudinal trend, and to sort out how this polymorphism relates to the ‘sexual races’ described in common frogs in the 1930s.     

Cytogenetics of ticks (Acari: Ixodoidea)

Haemaphysalis longicornis consists of diploid bisexual races (20+ XX; 20+X), triploid obligatory parthenogenetic races (30–35 chromosomes) and an aneuploid race capable of bisexual and parthenogenetic reproduction (22–28 chromosomes). Karyotypes were analyzed for each race. Hybridization failed between diploid and triploid races, but succeeded between bisexual diploid males and parthenogenetic aneuploid females. F₁ and F₂ progeny were produced and their chromosomes studied. Crossing of F₁ progeny to a bisexual race was successful. Parthenogenetic ability was almost completely lost in F₁ and F₂ females. Several possible modes of evolution from diploid bisexual individuals to triploid parthenogenetic ones are discussed as is species characterization in taxa with races reproducing bisexually, parthenogenetically and by a combination of both methods.Supported in part by National Science Foundation Research Grant GB-21008, National Institute of Allergy and Infectious Diseases (NIH) Grant 09556 and the United States Army Medical Research and Development Command, Office of The Surgeon General, Department of the Army, Washington, D. C. 20315, U.S.A.     

Behavioral and electrophysiological responses of Helicoverpa assulta, H. armigera (Lepidoptera: Noctuidae), their F1 hybrids and backcross progenies to sex pheromone component blends

Two sibling species, Helicoverpa assulta and Helicoverpa armigera both use (Z)-9-hexadecenal and (Z)-11-hexadecenal as their sex pheromone components but in almost reversed ratios, 93:7 and 3:97, respectively. H. assulta and H. armigera males performed upwind flight in response to the H. assulta sex pheromone blend (93:7). H. armigera responded strongly to the H. armigera blend (3:97), whereas H. assulta males remained inactive upon exposure to this blend. Both species gave clear dose-dependent electrophysiological responses to (Z)-11-hexadecenal. However, (Z)-9-hexadecenal evoked strong dose-dependent electrophysiological responses in H. assulta males but not in H. armigera. The two male F₁ hybrids exhibited similar behavioral responses to two sex pheromone blends and electrophysiological responses to two pheromone components as H. armigera males. This indicated that H. armigera genes appear dominant in determining the behavioral response and electrophysiological responses. Behavioral and electrophysiological responses of backcrosses of male F₁ hybrids (H. armigera female × H. assulta male) with female H. assulta and H. armigera were close to that of H. assulta and H. armigera, respectively. However, backcrosses of female F₁ hybrids (H. assulta female × H. armigera male) with male H. assulta and H. armigera showed reduced behavioral responses but normal electrophysiological responses compared to males of the respective parental line.     

CHARACTERIZATION OF GENETIC MARKERS LINKED TO SEX DETERMINATION IN THE HAPLOID‐DIPLOID RED ALGA GRACILARIA CHILENSIS1

Bulk segregant analysis, random amplified polymorphic DNA (RAPD), and sequence characterized amplified region (SCAR) methods were used to identify sex‐linked molecular markers in the haploid‐diploid rhodophyte Gracilaria chilensis C. J. Bird, McLachlan et E. C. Oliveira. One hundred and eighty 10 bp primers were tested on three bulks of DNA: haploid males, haploid females, and diploid tetrasporophytes. Three RAPD primers (OPD15, OPG16, and OPN20) produced male‐specific bands; and one RAPD primer (OPD12), a female‐specific band. The sequences of the cloned putative sex‐specific PCR fragments were used to design specific primers for the female marker SCAR‐D12‐386 and the male marker SCAR‐G16‐486. Both SCAR markers gave unequivocal band patterns that allowed sex and phase to be determined in G. chilensis. Thus, all the females presented only the female band, and all the males only the male band, while all the tetrasporophytes amplified both male and female bands. Despite this sex‐specific association, we were able to amplify SCAR‐D12‐386 and SCAR‐G16‐486 in both sexes at low melting temperature. The differences between male and female sequences were of 8%–9% nucleotide divergence for SCAR‐D12‐386 and SCAR‐G16‐486, respectively. SCAR‐D12‐386 and SCAR‐G16‐486 could represent degenerated or diverged sequences located in the nonrecombining region of incipient sex chromosomes or heteromorphic sex chromosomes with sequence differences at the DNA level such that PCR primers amplify only one allele and not the other in highly specific PCR conditions. Seven gametic progenies composed of 19 males, 19 females, and the seven parental tetrasporophytes were analyzed. In all of them, the two SCAR markers segregated perfectly with sexual phenotypes.     

Diploid male production in a leaf‐cutting ant

1. In haplodiploid social insects where males are haploid and females are diploid, inbreeding depression is expressed as the production of diploid males when homozygosity at the sex‐determining locus results in the production of diploid individuals with a male phenotype. Diploid males are often assumed to have reduced fitness compared with their haploid brothers. 2. While studying the reproductive biology of a leaf‐cutting ant, Atta sexdens, in Gamboa, Republic of Panama, we detected the presence of a larger male morph. Using microsatellite markers we were able to confirm that the large male morph was diploid in 87% of cases. 3. We infer that the Gamboa population of A. sexdens experiences inbreeding depression because diploid males were found in three out of five mature colonies. However, their frequencies were relatively low because queens were multiply mated and our estimates suggest that many diploid male larvae may not survive to adulthood. 4. We measured two traits potentially linked to male reproductive success: sperm length and sperm number, and showed that diploid males produced fewer but longer sperm. These results provide indirect evidence that diploid male reproductive success would be reduced compared with haploid males if they were able to copulate. 5. We conclude that diploid male production is likely to affect the fitness of A. sexdens queens with a matched mating, as these males are produced at the cost of workers and, if the colony survives to reach mature size, also gynes.     

Identifizierung der genetischen Geschlechtschromosomen bei der monogenen Schmeißfliege Chrysomya rufifacies (Calliphoridae,Diptera)

Previous investigations have shown the sex determination in the monogenic blowfly Chrysomya rufifacies to be controlled by a cytologically not discernible homogamety-heterogamety mechanism in the female. Female-producing (thelygenic) females are assumed to be heterozygous for a dominant female sex realizer (F′) with sex-predetermining properties, while male-producing (arrhenogenic) females as well as males are supposed to be homozygous for the recessive allele (f). In order to identify the genetic sex chromosomes of C. rufifacies among its five pairs of long euchromatic chromosomes (nos.1–5) plus one pair of small heterochromatic ones (no. 6), all chromosomes were marked by reciprocal translocations induced by X-ray treatment of adult males. The inheritance of thirteen different heterozygous translocations has been analyzed. All of the translocations (eleven) between two of the four longer chromosomes did not show sex-linked inheritance, thus demonstrating the autosomal character of the chromosomes nos 1, 2, 3 and 4. The same is true for the translocation T6 (2/6). Therefore the small heterochromatic chromosome no. 6, corresponding to the morphologically differentiated sex chromosomes within the amphogenic calliphorid species, remains without sex determining function in the monogenic fly. This could be confirmed by the analysis of monosomic (monosomy-6) and trisomic (trisomy-6) individuals, which resulted from meiotic non-disjunction in T6/+ translocation heterozygotes. Contrary to these translocations, the heterozygous 5/2 translocation (T14) exhibited sex-linked inheritance: There was but a very low frequency (0,76 per cent) of recombinants resulting from crossing-over between F′/f and the translocation breakage point in thelygenic F₁ T14/+ females. The sex-linked inheritance of T14 was confirmed by the progeny of a thelygenic F₁ T14/+ female crossed to a homozygous T14/T14 translocation male. Among the offspring of that F₁ T14/+ female, which had received the translocation from its father, all of the F₂ T14/+ females were thelygenic compared to their arrhenogenic T14/T14 sisters. These results prove that the chromosomes of pair no. 5 genetically act as X′X-XX sex chromosomes in C. rufifacies.     

Plasticity in life-history traits of the bark beetle Ips calligraphus as influenced by phloem thickness

Summary Reproduction and development of Ips calligraphus (Germar) (Coleoptera: Scolytidae) occur primarily in the phloem (inner bark) tissue of its pine hosts. In slash pine (Pinus elliottii Engelm. var. elliottii), phloem thickness can vary widely from tree to tree. We compared adult residence time and fecundity and progeny development time, body size, and sex ratio of this beetle when reared in slash pine bolts and bark slabs with phloem thicker or thinner than average adult body width. Most studies were conducted at 20°, 25°, and 30° C. Residence time of parent males and females decreased with increasing temperature but it was not affected by phloem thickness. Residence time of parent males was about 2 days shorter than that of parent females at each temperature. Reproductive fitness was greater in thick phloem at all temperatures as measured by faster larval development, earlier emergence of progeny (F ₁ ) adults, and emergence of more progeny adults per parent female. Progeny survival was similar between phloem those from thick phloem, and their sex ratio was female biased (1:2 vs 1:1, male:female). When allowed to inhabit thick phloem, the progeny (F ₂) of adults from thin phloem were just as large and of similar sex ratio (1:1) as were progeny of F ₁ adults from thick phloem. The high degree of plasticity in the life-history traits of this beetle may enable it to successfully colonize pines that vary widely in phloem thickness.     

Nucleolus size varies with sex,ploidy and gene dosage in insects

The nucleolus constitutes a cytologically visible phenotype for ribosomal DNA (rDNA). Nucleolar size, as determined by silver staining, is a good indicator of cell proliferation rate and biosynthetic activity. Nevertheless, the relationship between rDNA content and sexual dimorphism for nucleolar size is not well documented. In the present study, the impact of sex and ploidy level on nucleolar size is investigated in three haplo/diploid and three diplo/diploid species of insect. Nucleolar sizes are found to be proportional to ploidy level in the haplo/diploid hymenopterans Trypoxylon albitarse and Nasonia vitripennis. Conversely, in the ant Messor barbarus, nucleolar sizes are larger in haploid males (winged) than diploid females (apterous). Among the diplo/diploid species, evidence for gene dosage compensation on nucleolar activity is suggested by the absence of sex differences in Drosophila simulans, a species in which rDNA is limited to the X chromosome. By contrast, in the grasshopper Stenobothrus festivus, another species with rRNA genes restricted to the X chromosome, the size of the nucleolus is significantly larger in females than in males. Additionally, in the grasshopper Chorthippus parallelus, where rDNA is distributed evenly on several autosomes of males and females, the females also show larger nucleoli than males. In both grasshopper species, the magnitude of the female/male ratio for nucleolus area is very similar to the body size ratio, suggesting that body size, as well as sex, ploidy, gene dosage and physiological activity, may be an important determinant of nucleolus area.     

Diploid arrhenotoky and automictic thelytoky in soft scale insects (Lecaniidae: Coccoidea: Homoptera)

Parthenogenesis is reported in three soft scales with 2n=16. In the unfertilized eggs of all three, oogenesis is normal and diploidy is restored by the fusion of the division products of the haploid female pronucleus. In Lecanium putmani Phillips 12 of 13 uninseminated females collected in the wild produced only males. The 21 inseminated females produced 15% males. The males were diploid but contained one euchromatic (E) and one heterochromatic (H) chromosome set. Most of the eggs produced by the inseminated females contained sperm but a few did not. It was concluded, therefore, that females develop from fertilized eggs and males from unfertilized eggs and that the species was diploid arrhenotokous. In L. cerasifex Fitch only 18 of 56 females collected in the wild had been inseminated. The frequency of males among their embryos was 22%. The males were again diploid with one E and one H set of chromosomes. Among the 38 uninseminated females, 27 produced only males, and 10 produced only females. All the female producers contained needle-like bacterial symbionts. Most of the male producers, and most of the inseminated females contained no symbionts; the rest contained rod-like symbionts. It was concluded, therefore, that the females of L. cerasifex studied belonged to two races, a diploid arrhenotokous race and an obligate automictic thelytokous race. Eucalymantus tessellatus (Signoret) is obligate automictic thelytokous. All the females examined were uninseminated and produced only females.Supported by Grant GB 23665 from the National Science Foundation, Washington, D.C.     

Phenotypic fitness effects of the selfish B chromosome,paternal sex ratio (PSR) in the parasitic waspNasonia vitripennis

Summary B chromosomes are often considered genomic parasites. Paternal sex ratio (PSR) is an extreme example of a parasitic B chromosome in the parasitoid waspNasonia vitripennis. PSR is transmitted through the sperm of carrier males and destroys the other paternal chromosomes in early fertilized eggs. PSR disrupts the normal haplodiploid sex determination in this wasp by converting diploid (female) eggs into haploid (male) eggs that bear PSR. In this study I compare a number of phenotypic fitness aspects of PSR and standard (non-PSR) males. In general, PSR males were as fit as standard males. No significant differences were found in longevity (with one exception), ability to compete for mates and sperm depletion rates. PSR males produced 11–22% larger family sizes and developed slightly faster than standard males. Under conditions of sperm competition, females who mated with both types of males fertilized a constant proportion of eggs with each sperm type over their lifetime. PSR males produced fewer offspring among progenies from double-inseminated females. Phenotypic fitness effects are believed to play a minor role in determining PSR frequencies in natural populations.     

Chromosomal differentiation in two species of Aedes and their hybrids revealed by giemsa C-banding

Giemsa C-banding patterns in two species of mosquitoes, Aedes aegypti and Aedes mascarensis, their hybrids and backcross progeny revealed differences in the sex chromosome pair. In A. aegypti, the female determining or the m chromosome in both males and females shows a conspicuous band in the centromere region and another band in one arm. The male determining or the M chromosome is devoid of any bands. Progeny of crosses involving A. aegypti females and A. mascarensis males showed interesting albeit unexpected results. The intercalary band was suppressed in both sons and daughters. When such F₁ sons were backcrossed to A. aegypti females, a proportion of males developed into intersexes. These intersex progeny differed from the normal males in terms of their banding pattern. In the reciprocal cross (A. mascarensis female × A. aegypti male), the F₁ and the backcross progeny yielded the expected C-banding patterns. The implications of the reversible expression of the intercalary band on the A. aegypti m chromosome and its relevance to genetic regulation are discussed.     

Sex, bugs and Haldane's rule: the nematode genus Pristionchus in the United States

The haplodiploid sex determining mechanism in Hymenoptera (males are haploid, females are diploid) has played an important role in the evolution of this insect order. In Hymenoptera sex is usually determined by a single locus, heterozygotes are female and hemizygotes are male. Under inbreeding, homozygous diploid and sterile males occur which form a genetic burden for a population. We review life history and genetical traits that may overcome the disadvantages of single locus complementary sex determination (sl-CSD). Behavioural adaptations to avoid matings between relatives include active dispersal from natal patches and mating preferences for non-relatives. In non-social species, temporal and spatial segregation of male and female offspring reduces the burden of sl-CSD. In social species, diploid males are produced at the expense of workers and female reproductives. In some social species, diploid males and diploid male producing queens are killed by workers. Diploid male production may have played a role in the evolution or maintenance of polygyny (multiple queens) and polyandry (multiple mating). Some forms of thelytoky (parthenogenetic female production) increase homozygosity and are therefore incompatible with sl-CSD. We discuss a number of hypothetical adaptations to sl-CSD which should be considered in future studies of this insect order.