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Pre-mating injection of an analogue of gonadotrophin-releasing hormone (GnRH) and pregnancy rates to first insemination.

Two hundred and ninety two dairy cows received a subcutaneous injection of a 2.5 ml solution containing 10 microg GnRH-analogue (Receptal, Hoechst A.G.) 0-6 hours before insemination, while 284 cows acting as controls were injected with 2.5 ml of sterile pyrogen-free water at the same time. The two groups, the treated and the control, were formed by matching (pairing) each oestrous cow with another on the basis of interval from calving to first mating, condition score, and age on the day of first mating after calving. The cows were in 3 factory supply dairy herds, which were visited daily during the first 3 weeks of the mating season. All the cows presented for mating each day were inseminated by the same technician using 0.5 ml of ambient-temperature semen containing 2 million spermatozoa per insemination. The semen used on any particular day originated from one ejaculate of one bull (same batch number). The cows were manually examined for pregnancy 2 to 3 months after their first insemination. A similar response was seen in all three herds irrespective of the interval from calving to mating. First mating pregnancy rates were 9.3% higher in the Receptal-treated cows than in the control group (P = 0.025). It is suggested that Receptal may have a beneficial effect on the pregnancy rate of cows that have recently ovulated as well as on those having delayed ovulation.

Animals↗

Arousal, personality, and assortative mating in marriage.

It is known that there is significant assortative mating for intelligence. However, where personality is concerned, the picture is less clear, and where physiologically referenced individual differences are concerned, there is a negligible body of available research. A compound major individual difference variable having a putative physiological basis--arousal and the stimulation-seeking motive, which has not heretofore been investigated in studies of assortative mating--was the focus of the present study. In addition, three major personality dimensions--extraversion-introversion, neuroticism and psychoticism--were included for study. One hundred and two married couples in the housing complex of a large American midwestern university were tested on the arousal/stimulation-seeking and personality measures. Significant assortative mating (p less than .01) was found only for arousal/stimulation-seeking. The results for the other personality dimensions failed to confirm significant but slight assortative mating for neuroticism and psychoticism previously reported for British couples, but were in accord with the previously reported lack of any assortative mating for extraversion-introversion. The results were discussed in terms of further understanding the basis of assortative mating, with particular attention given to the likely role of biological cycles. Further research was outlined.

Adaptation, Psychological↗

Radiation-induced mating-type switching in the yeast Saccharomyces cerevisiae.

Haploid yeast cells possess two different mating types which are controlled genetically by the MAT locus. Information of the opposite mating type is stored on the same chromosome but not expressed. Radiation may initiate a gene conversion event leading to 'mating-type switching'. This was studied by using X-rays and 254 nm ultraviolet light. X-ray-induced mating type switching shows an oxygen enhancement ratio of 2.9 which is higher than that for survival (1.8) and equals that for double-strand break induction. Mating-type switching by UV is not photoreactivable and depends on a functioning excision repair system. The results are compatible with the interpretation that mating type switching is initiated by a double-strand break in the MAT coding region.

Gene Conversion↗

Required parental investment and mating patterns: a quantitative analysis in the context of evolutionarily stable strategies.

Much social psychological research has been dedicated to understanding mating strategies from the standpoint of genetic-fitness payout (e.g., Simpson and Gangestad, 2000). The current work is designed to provide a coherent, quantitative model for predicting different classes of mating strategies in both males and females. Specifically, the framework developed in this paper is an elaboration of Dawkins' (1989) quantitative assessment of different male and female mating strategies. Dawkins suggests that the prevalence of different strategies employed should be predictable in terms of evolutionary stable strategies. In the current work, a quantitative analysis predicting the prevalence of different mating strategies within each sex was conducted. The mathematical functions derived suggest that variability in the costs associated with raising offspring affects the expected prevalence of mating strategies differently for males and females. According to the present model, variability in female strategies should be less affected by changes in parental investment (PI) than variability in male strategies. Important predictions regarding male and female mating strategies across cultures are discussed.

Biological Evolution↗

Spodoptera exigua: mating disruption, measurement of airborne concentration of pheromone, and use of specialist receptor cell responses for comparison to female pheromone emission.

Field experiments were conducted to evaluate Shin-Etsu Yoto-con-S 'rope' pheromone dispensers applied at different site densities in cotton to determine efficacy in disrupting sexual communication and mating of beet armyworm moths, Spodoptera exigua (Hübner); obtain atmospheric measurements of the disruptant pheromone components in and away from treated areas; and relate this information to estimates of the concentration of pheromone in the near vicinity of a calling virgin female moth. The number of pheromone-dispensing sites/ha ranged from 25 with 20 ropes/site up to a total of 247 sites with 2 ropes each. A total of 112 g pheromone of a 70:30 blend of (Z,E)-9,12-tetradecadien-l- ol acetate (ZETA) and (Z)-tetradecen-1-ol (Z9-14:OH) was applied/ha. As few as 25 sites/ha effectively disrupted sexual communication by 91%, as measured by reductions of moth captures in traps baited with pheromone lures, and mating by beet armyworm females by 94% for at least 10 weeks post-treatment. The results compared favorably to an earlier large-scale field experiment in which beet armyworm larval populations were reduced 95% using 500 pheromone-dispensing sites/ha (two ropes/site) and 160 g total pheromone/ha. The airborne concentration of ZETA and Z9-14:OH measured within the pheromone-treated plots that disrupted mating was 1.5 x 10(-13) M and 1.2 x 10(-13) M, respectively. The airborne concentration of ZETA and Z9-14:OH in the vicinity of a female was estimated (by excision and electrophysiological methods) to range between 2.1 x 10(-11) M and 2.4 x 10(-12) M, respectively, in a 1.6 km/h (1 mph) wind speed. Thus, the average ZETA concentration in the treated plots was about 140 times less than that expected from a single female; the average Z9-14:OH in the treated plots was about 20 times less. The data support an argument that disruption of mating by beet armyworm resulted from an imbalance in sensory input because mating was almost completely disrupted in all of the plots for at least 10 weeks with a mixture of ZETA:Z9-14:OH that differed significantly with that from excised female sex pheromone glands. Estimates of these parameters provide a benchmark for the requisite pheromone concentration in the atmosphere to achieve a high level of mating disruption for beet armyworm and possibly other insect pest species.

Air↗

Prm1p, a pheromone-regulated multispanning membrane protein, facilitates plasma membrane fusion during yeast mating.

Cell fusion occurs throughout development, from fertilization to organogenesis. The molecular mechanisms driving plasma membrane fusion in these processes remain unknown. While yeast mating offers an excellent model system in which to study cell fusion, all genes previously shown to regulate the process act at or before cell wall breakdown; i.e., well before the two plasma membranes have come in contact. Using a new strategy in which genomic data is used to predict which genes may possess a given function, we identified PRM1, a gene that is selectively expressed during mating and that encodes a multispanning transmembrane protein. Prm1p localizes to sites of cell-cell contact where fusion occurs. In matings between Deltaprm1 mutants, a large fraction of cells initiate zygote formation and degrade the cell wall separating mating partners but then fail to fuse. Electron microscopic analysis reveals that the two plasma membranes in these mating pairs are tightly apposed, remaining separated only by a uniform gap of approximately 8 nm. Thus, the phenotype of Deltaprm1 mutants defines a new step in the mating reaction in which membranes are juxtaposed, possibly through a defined adherence junction, yet remain unfused. This phenotype suggests a role for Prm1p in plasma membrane fusion.

Amino Acid Sequence↗

Sexual conjugation in yeast. Cell surface changes in response to the action of mating hormones.

In the yeast Saccharomyces cerevisiae, sexual conjugation between haploid cells of opposite mating type results in the formation of a diploid zygote. When treated with fluorescently labeled concanavalin A, a zygote stains nonuniformly, with the greatest fluorescence occurring at the conjugation bridge between the two haploid parents. In the mating mixture, unconjugated haploid cells often elongate to pear-shaped forms ("shmoos") which likewise exhibit asymmetric staining with the most intense fluorescence at the growing end. Shmoo formation can be induced in cells of one mating type by the addition of a hormone secreted by cells of the opposite mating type; such shmoos also stain asymmetrically. In nearly all cases, the nonmating mutants that were examined stained uniformly after incubation with the appropriate hormone. Asymmetric staining is not observed with vegetative cells, even those that are budded. These results suggest that, before and during conjugation, localized cell surface changes occur in cells of both mating types; the surface alterations facilitate fusion and are apparently mediated by the hormones in a manner that is mating-type specific.

Cell Wall↗

Evolution of male parental care and female multiple mating: game-theoretical and two-locus diploid models.

Males gain a fitness benefit by mating with many females, whereas the number of progeny per female does not increase as a function of additional mates. Furthermore, males run the risk of investing in the offspring of other males if they provide parental care. Nevertheless, in various species, males provide parental care, and females mate with multiple males. We investigate a game-theoretical model in which females gain a direct benefit by multiple mating from the paternal care they elicit for their offspring. The parameters that directly favor male parental care, such as small cost of paternal care, have indirect positive effects on the evolution of female multiple mating, while they have negative effects in the opposite case. Both traits are more likely to evolve when the number of matings is smaller. The individual-based model of a diploid two-locus, two-allelic genetic model confirms the result.

Animals↗

A cognitive framework for mate choice and species recognition.

Mating decisions contribute to both the fitness of individuals and the emergence of evolutionary diversity, yet little is known about their cognitive architecture. We propose a simple model that describes how preferences are translated into decisions and how seemingly disparate patterns of preference can emerge from a single perceptual process. The model proposes that females use error-prone estimates of attractiveness to select mates based on a simple decision rule: choose the most attractive available male that exceeds some minimal criterion. We test the model in the tungara frog, a well-characterized species with an apparent dissociation between mechanisms of mate choice and species recognition. As suggested by our model results, we find that a mate attraction feature alters assessments of species status. Next, we compare female preferences in one-choice and two-choice tests, contexts thought to emphasize species recognition and mate choice, respectively. To do so, we use the model to generate maximum-likelihood estimators of preference strengths from empirical data. We find that a single representation of preferences is sufficient to explain response probabilities in both contexts across a wide range of stimuli. In this species, mate choice and species recognition are accurately and simply summarized by our model. While the findings resolve long-standing anomalies, they also illustrate how models of choice can bridge theoretical and empirical treatments of animal decisions. The data demonstrate a remarkable congruity of perceptual processes across contexts, tasks, and taxa.

Animals↗

Herbivory and competition interact to affect reproductive traits and mating system expression in Impatiens capensis.

As a step toward understanding how community context shapes mating system evolution, we investigated the combined role of two plant antagonisms, vegetative herbivory and intraspecific competition, for reproduction and mating system expression (relative production of selfing, cleistogamous and facultatively outcrossing, chasmogamous flowers and fruits) of Impatiens capensis. In a survey of I. capensis populations, we found that vegetative herbivory and intraspecific competition were positively correlated. In a greenhouse experiment where leaf damage and plant density were manipulated, multispecies interactions had dramatic effects on reproductive and mating system traits. Despite having additive effects on growth, herbivory and competition had nonadditive effects for mating system expression, chasmogamous fruit production, flower number and size, and cleistogamous flower production. Our results demonstrate that competitive interactions influence the effect of herbivory (and vice versa) on fitness components and mating system, and thus antagonisms may have unforeseen consequences for mating system evolution, population genetic diversity, and persistence.

Ecosystem↗

HLA and mate selection: no evidence in South Amerindians.

There have been reports of nonrandom mating (negative-assortative mating) or preference for individuals of different major histocompatibility complex (MHC) genotypes in both mice and humans. We have examined the association of HLA-A and HLA-B genotypes, both for each locus by itself and for two-locus genotypes, in mates of 194 couples from 11 South Amerindian tribes. The proportion of couples sampled averaged >50% of the total matings with progeny for 10 of the tribes. In nearly all cases, HLA-sharing proportions were very close to those expected from random mating, suggesting strong negative-assortative mating for MHC is not present in these South Amerindians.

Female↗

Effects of arousal from hibernation and plasma androgen levels on mating behavior in the male big brown bat, Eptesicus fuscus.

The effects of arousal from hibernation and presence of plasma androgen on the expression of mating behavior in male big brown bats (Eptesicus fuscus) were tested in a captive population exposed to seminatural conditions in central Alabama. In the mild winter of 1994-1995, flight cage temperatures never fell below 10 degrees C. Bats were never observed to enter sustained (over 2 d) torpor. They were also never observed to mate. Unmanipulated, sham-operated, and gonadectomized males and unmanipulated females were exposed to 6 d of 4 degrees C. All individuals appeared torpid, and body temperatures of monitored bats fell at least 15 degrees-20 degrees C. Plasma androgen levels of torpid unmanipulated, sham-operated, and gonadectomized males averaged 25.4 +/- 9.2, 19.7 +/- 9.1, and 1.5 +/- 0.25 ng/mL, respectively, and did not differ significantly from levels for the same groups 1 mo previous to induced torpor. When animals were returned to 23 degrees C, 57% of unmanipulated, 40% of the sham-operated, and 33% of gonadectomized males displayed mating behavior upon arousal. Almost all matings occurred within 48 h of arousal, the majority in the first 3 h. Males not exposed to low temperatures were not observed to mate. Although individuals from all three treatments mated, gonadectomized males averaged fewer mounts and copulations per individual. Androgen levels declined significantly from torpor levels in all groups 48 h after arousal. Thus, an extended period of low body temperature and arousal appeared to be a short-term activator of sexual behavior in the big brown bat; unmanipulated males were more strongly affected by this stimulus than gonadectomized males.

Androgens↗

An essential gene pair in Saccharomyces cerevisiae with a potential role in mating.

In the yeast Saccharomyces cerevisiae, the signal generated by extracellular pheromone is transmitted through the beta and gamma subunits of a trimeric G-protein to downstream signaling molecules that mediate the cellular responses associated with mating. To isolate potential downstream signaling components, a yeast genomic library on a multicopy plasmid was screened for genes that increased the mating efficiency of a strain containing a temperature-sensitive G beta subunit mutation. Overexpression of STE5, STE18 (which encodes the G gamma subunit), and a previously unidentified gene, termed SSF1, partially suppressed the mating defect of a G beta mutant. Hybridization of yeast genomic DNA with an SSF1 probe revealed a closely related homolog, termed SSF2, which was isolated and also found to test positively in the assay for suppression. Null mutations in either SSF1 or SSF2 had no obvious phenotype, but disruption of both genes was lethal. Depletion of SSF gene products from growing cultures caused both an arrest of cell division and a significant decrease in the ability of cells to mate. Because mating efficiency was increased by extra copies of the SSF genes and decreased by elimination of the gene products, it is likely that these genes play a role in mating as well as in an essential function.

Amino Acid Sequence↗

FUS1 regulates the opening and expansion of fusion pores between mating yeast.

Mating yeast cells provide a genetically accessible system for the study of cell fusion. The dynamics of fusion pores between yeast cells were analyzed by following the exchange of fluorescent markers between fusion partners. Upon plasma membrane fusion, cytoplasmic GFP and DsRed diffuse between cells at rates proportional to the size of the fusion pore. GFP permeance measurements reveal that a typical fusion pore opens with a burst and then gradually expands. In some mating pairs, a sudden increase in GFP permeance was found, consistent with the opening of a second pore. In contrast, other fusion pores closed after permitting a limited amount of cytoplasmic exchange. Deletion of FUS1 from both mating partners caused a >10-fold reduction in the initial permeance and expansion rate of the fusion pore. Although fus1 mating pairs also have a defect in degrading the cell wall that separates mating partners before plasma membrane fusion, other cell fusion mutants with cell wall remodeling defects had more modest effects on fusion pore permeance. Karyogamy is delayed by >1 h in fus1 mating pairs, possibly as a consequence of retarded fusion pore expansion.

Cell Membrane↗

A general algorithm to compute multilocus genotype frequencies under various mating systems.

This paper provides a general method to derive algebraic expressions of genotype frequencies for multiple loci under various mating systems, including random mating, back-crossing, selfing, and full-sib mating. For each mating system, general equations are presented. In the case of three loci, comprehensive tables provide recurrence equations for genotype frequencies under random or self mating, and expected genotype frequencies after two generations of full-sib mating. Our results should prove useful in genetic linkage analysis.

Algorithms↗

Pseudo-random mating populations. In celebration of the 80th anniversary of the Hardy-Weinberg law.

That random mating leads to Hardy-Weinberg distribution of genotypes is well known. This report is to show that, if the deviations from random mating are of a certain pattern, the offspring generation will also be in Hardy-Weinberg proportions. This brings out the fact that random mating is a sufficient condition, not a necessary one, for the attainment of the Hardy-Weinberg proportions. Such nonrandom-mating populations are tentatively said to be pseudo-random mating. Pseudo-random-mating populations exist for both autosomal and sex-linked systems with two or multiple alleles. This report covers the basic case of a two-allele autosomal locus in detail, but the possible extension to two loci and cytonuclear systems have also been mentioned in discussion.

Alleles↗

On the theory of partially inbreeding finite populations. II. Partial sib mating.

It is assumed that a population has M males in every generation, each of which is permanently mated with c-1 females, and that a proportion beta of matings are between males and their full sisters or half-sisters. Recurrence equations are derived for the inbreeding coefficient of one random individual, coefficients of kinship of random pairs of mates and probabilities of allelic identity when the infinite alleles model holds. If Ft is the inbreeding coefficient at time t and M is large, (1-Ft)/(1-Ft-1)----1-1/(2Ne) as t increases. The effective population number Ne = aM/[1 + (2a-1)FIS], where FIS is the inbreeding coefficient at equilibrium when M is infinite and the constant a depends upon the conditional probabilities of matings between full sibs and the two possible types of half-sibs. When there are M permanent couples, an approximation to the probability that an allele A survives if it is originally present in one AA heterozygote is proportional to FISs1 + (1-FIS)s2, where s1 and s2 are the selective advantages of AA and AA in comparison with AA. The paper concludes with a comparison between the results when there is partial selfing, partial full sib mating (c = 2) and partial sib mating when c is large.

Alleles↗

A filamentous growth response mediated by the yeast mating pathway.

Haploid cells of the budding yeast Saccharomyces cerevisiae respond to mating pheromones by arresting their cell-division cycle in G1 and differentiating into a cell type capable of locating and fusing with mating partners. Yeast cells undergo chemotactic cell surface growth when pheromones are present above a threshold level for morphogenesis; however, the morphogenetic responses of cells to levels of pheromone below this threshold have not been systematically explored. Here we show that MATa haploid cells exposed to low levels of the alpha-factor mating pheromone undergo a novel cellular response: cells modulate their division patterns and cell shape, forming colonies composed of filamentous chains of cells. Time-lapse analysis of filament formation shows that its dynamics are distinct from that of pseudohyphal growth; during pheromone-induced filament formation, daughter cells are delayed relative to mother cells with respect to the timing of bud emergence. Filament formation requires the RSR1(BUD1), BUD8, SLK1/BCK1, and SPA2 genes and many elements of the STE11/STE7 MAP kinase pathway; this response is also independent of FAR1, a gene involved in orienting cell polarization during the mating response. We suggest that mating yeast cells undergo a complex response to low levels of pheromone that may enhance the ability of cells to search for mating partners through the modification of cell shape and alteration of cell-division patterns.

Cell Division↗