SEARCH · PubMed Health

Results for “mating”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 37 records · Page 2Linked to original sources

PubMed1976

Assortative mating in lesser snow geese (Anser caerulescens).

Assortative mating occurs in the dimorphic lesser snow geese in the wild. Mixed matings between the blue and white phases are much less frequent than would be expected by chance. Evidence from marked birds in field conditions indicated that mate choice was correlated with familial color. Birds from white families usually chose white mates, birds from blue families usually chose blue mates, and birds from mixed families chose mates of either color. Similar results were obtained under captive conditions when offspring from foster families with particular parental and offspring color combinations were allowed to choose mates. Both parental color and sibling color appeared to influence mate choice. The bird's own color did not appear to be important in mate choice in either field or experimental conditions, and in those cases where male and female parents differed in color neither parental color was more influential than the other in determining offspring mate choice. The results provide the first evidence, to our knowledge, that mate selection based on familial appearance operates intraspecifically in the wild.

Animals↗

PubMed1979

Quantitative analysis of mating behavior in aging male Drosophila melanogaster.

Dynamic changes in quantitative aspects of mating behavior of the male fruit fly as its life unfolds, from eclosion through maturity (peak performance) and "physiological death" (loss of fertility followed by complete loss of ability to mate), towards actual death, have been identified in this work by observations and measurements on 28 male fruit flies of the Oregon R strain studied individually. At weekly sessions from the first day of their imaginal life until their natural death, each fly was given the opportunity to mate with up to three virgin females during a one-hour period. Length of the latency period of each accomplished mating and duration of copulation were recorded. After mating the females were allowed to lay eggs for 24 hours and the number of offspring was counted 26 days later. The period between 1 and 4 weeks of age is characterized by peak and fairly constant performance: multiple matings, short latencies, long durations of copulation, and high degree of fertility (number of offspring); then a decline sets in, in some measures slower than in others, as the flies age. Large intra- and inter-individual variabilities were, however, found which obscure possible correlations between individual measures of mating ability and length of life. At the individual level, a preliminary analysis showed a good correlation (r = 0.80 and 0.79) between life span and week of last mating (onset of impotence) or week of last fertile mating (onset of sterility). At the population level it was found that a number of measures, i.e. number of remaining maters at each age, number of remaining fertile maters and total number of matings, had an age-course similar to survivorship but anticipated it by 4--6 weeks. Other measures, such as number of multiple matings and number of offspring declined with age faster than survivorship.

Aging↗

PubMed1975

Morphological change in the early stages of the mating process of Rhodosporidium toruloides.

The events which occur in the early stages of the mating process of the yeast Rhodosporidium toruloides between strains M-919 (mating type A) and M-1057 (mating type a) were investigated. In preliminary experiments we determined the frequency of mating by two newly designed methods: the liquid culture method and the membrane-filter microculture method. The mating frequencies of strains M-919 and M-1057 were 89% in the liquid culture method and 62% in the membrane-filter microculture method. The early stages in the mating process included the following events: (i) M-919 cells produce constitutively the extracellular inducing substance (A factor), (ii) M-1057 cells receive A factor, and in response to it they form mating tubes and secrete another inducing substance (a factor), (iii) M-919 cells receive a factor, and in response to it they form mating tubes, (iv) mating tubes elongate to the cells or the tubes of mating partner, (v) tips of the growing tubes recognize the opposite mating type cells or their tubes, followed by cell-to-cell fusion.

Basidiomycota↗

PubMed1975

Mating aggregates in Escherichia coli conjugation.

Mating mixtures of Escherichia coli cells were shown to contain mating aggregates of two to 20 cells each rather than only mating pairs of two cells each. The mating aggregate size distribution shows two broad peaks, at two to four cells and at eight to 13 cells. The quantitative mating aggregate size distribution and the proportion of male cells in mating aggregates are dependent on the input ratio of male to female cells. At an input ratio of one to one, the average mating aggregate contains equal proportions of male and female cells and most of the cells involved in mating are in large aggregates of seven or more cells each. The deoxyribonucleic acid (DNA) transfer efficiency per mating aggregate cell was constant regardless of average aggregate size or of the ratio of male to female cells in the aggregate. Under optimal conditions essentially every male cell or every female cell in a mating aggregate can be involved in DNA transfer. A comparison of light microscopy, sucrose gradient centrifugation, and analysis with a modified Coulter counter indicated that the number of cells in mating aggregates is best equantitated using a modified Coulter counter.

Cell Aggregation↗

PubMed1975

Relative mating activity of the sexes in homokaryotypes of Drosophila persimilis from a Redwoods population.

Previous tests for mating activity of Drosophila persimilis homokaryotype KL (Klamath) and MD (Mendocino) chromosomal arrangements (northern California population: Redwoods) had shown KL to mate faster on the average than MD in homogamic tests. A strain (double-cross hybrid of four KL lines from the same population) with reliable high mating activity was developed for testing the sexes separately. Five pairs of KL-MD homokaryotype strains were chosen to be tested by the criterion that each pair had been derived from a separate wild KL/MD progenitor. Strains were crossed within arrangements in a diallelic design (20 inter- and five intrastrain crosses tested in 16 replicates per cross) to provide mating activity indices of four sets: KL females, KL males, MD females, MD males. Mating tests employed ten virgin experimental flies with ten tester (double-cross hybrid) flies of the opposite sex in 30-min observation periods. All flies were matured for 5 days at 25 degrees C before testing. Among parental strains, females were consistently higher in mating activity than males for both KL and MD arrangements. Most interstrain hybrids were heterotic, with KL and MD females not significantly different. However, hybrid MD males displayed greatest variation and had lowest mating activity, while KL males were the least variable and highest in mating activity. With heterosis in the hybrids, there was no predictability (additivity) from performance of parental strains to hybrid offspring. Mating activities of the two sexes were uncorrelated, indicating either that the sexes have independent genetic systems controlling mating activity or that the expression of the same genetic system is influenced by sex. Since the hybrid males of the two karyotypes displayed different courtship activity while the females were at about an equal level of receptivity, intrasexual selection among males is likely to be important in nature.

Alleles↗

PubMed1977

Regulation of mating in the cell cycle of Saccharomyces cerevisiae.

The capacity of haploid a yeast cells to mate (fuse with a haploid strain of alpha mating type followed by nuclear fusion to produce a diploid cell) was assessed for a variety of temperature-sensitive cell division cycle (cdc) mutants at the permissive and restrictive temperatures. Asynchronous populations of some mutants do not mate at the restrictive temperature, and these mutants define genes (cdc 1, 4, 24, and 33) that are essential both for the cell cycle and for mating. For most cdc mutants, asynchronous populations mate well at the restrictive temperature while populations synchronized at the cdc block do not. Populations of a mutant carrying the cdc 28 mutation mate well at the restrictive temperature after synchronization at the cdc 28 step. These results suggest that mating can occur from the cdc 28 step, the same step at which mating factors arrest cell cycle progress. The cell cycle interval in which mating can occur may or may not extend to the immediately succeeding and diverging steps (cdc 4 and cdc 24). High frequency mating does not occur in the interval of the cell cycle extending from the step before the initiation of DNA synthesis (cdc 7) through DNA synthesis (cdc 2, 8, and 21), medial nuclear division (cdc 13), and late nuclear division (cdc 14 and 15).

Cell Cycle↗

PubMed1977

Effect of entry exclusion on mating aggregates and transconjugants.

Mating aggregates during conjugation directed by an F-like R factor in Escherichia coli were measured as the number of Lac+-Lac- sectored colonies present in a mating mixture. There is a high degree of correlation between the concentration of transconjugants produced in a mating mixture and the concentration of mating aggregates observed at several different concentrations of donor and recipient cells. The mating aggregates are sex pilus specific as demonstrated by the ability of donor-specific ribonucleic acid phage MS-2 to decrease both mating aggregates and transconjugants in a mating mixture. During entry exclusion by either a derepressed or a repressed F-like R factor, isogenic to the superinfecting R factor except for a resistance determinant, the number of transconjugants was markedly reduced, but the number of mating aggregates was not decreased. Entry exclusion by F-Gal toward the donor HfrH resembled that of the F-like R factor in that there was a reduction in the number of recombinants but no significant decrease in mating aggregates. These results suggest that entry exclusion inhibits conjugation at a stage after the formation of mating aggregates.

Conjugation, Genetic↗

PubMed1978

Reaction order of Saccharomyces cerevisiae alpha-factor-mediated cell cycle arrest and mating inhibition.

Alpha-factor-mediated cell cycle arrest and mating inhibition of a mating-type cells of Saccharomyces cerevisiae have been examined in liquid cultures. Cell cycle arrest may be monitored unambiguously by the appearance of morphologically abnormal cells after administration of alpha factor, whereas mating inhibition is determined by comparing the mating efficiency in the absence or presence of added alpha factor. For both cell cycle arrest and mating inhibition, a dose-dependent response may be observed at limiting concentrations of the pheromone. If cell cycle arrest and mating inhibition require a small number of alpha-factor molecules, one might expect that responsive/nonresponsive cells = K(alpha factor)(N) where N is the order of dependence of cell cycle arrest (or mating inhibition) on alpha-factor concentration. The value of N has been determined to be 0.98 +/- 0.18 (standard error of the mean) for cell cycle arrest and 1.08 +/- 0.32 for mating inhibition. These results support the notion that saturation of a single site by alpha factor is sufficient to cause cell cycle arrest or mating inhibition of a mating-type cells.

Cell Cycle↗

PubMed1977

Social organization and mating success in local song populations of village indigobirds, Vidua chalybeata.

Behavioral interactions among color-marked individual Vidua chalybeata that shared common song dialects were observed for 5 years in two populations at Lochinvar National Park, Zambia. Social interactions involved males visiting and competing for mating sites and female visiting male in an apparent sampling of potential copulating partners. Differences in mating success among the polygynous males were compared with male behavior and territory resources, and criteria were developed to test the importance of intrasexual male competition and female mate choice in explaining the mating system of the populations. Song behavior best explained differences in mating success of males, with lesser effects of neighboring males and the defensible resources around the call-sites. The social organization of song populations resembles that of a dispersed lek with females visiting many males but mating with few males. We discuss the observations on indigobirds in relation to behavioral selection, sexual selection, and mating systems. Mating systems of certain populations and species are compared using statistics of individual mating success.

Aggression↗

PubMed1978

Cell-cell recognition in Saccharomyces cerevisiae: regulation of mating-specific adhesion.

Mating-specific adhesion between haploid yeast cells of opposite mating type (a and alpha) was studied by using a quantitative agar plate assay. Washed a and alpha cells that had not previously been exposed to their respective opposite mating type ("naive" cells) adhered relatively weakly. In water, only 5 to 10% of the a cells stuck tightly enough to alpha cells to give rise subsequently to diploid clones on the assay plates. Under optimum conditions (pH 6 to 7, at least 0.1 M Nacl or 0.01 M Mg(2+)), there was about 20% adhesion. Nevertheless, this weak binding defined a mating type-specific interaction because, even under optimum conditions, the homologous interactions (a with a and alpha with alpha) yielded only 3 to 5% cohesion. In contrast to these results, washed cells that had been preincubated in the cell-free culture medium of their opposite mating type ("preconditioned" cells) adhered quite strongly. The degree of adhesion between preconditioned cells (40 to 50%) was essentially unaffected by extremes of ionic strength, pH, and temperature and by the absence of divalent cation. This strong interaction was also mating type specific since cohesion between preconditioned cells of like mating type was only about 5%. The increase in agglutinability was obtained if only the a cells were preconditioned and could be induced by highly purified preparations of natural or synthetically prepared alpha-factor, an oligopeptide pheromone released by the alpha cells. The appearance of increased adhesiveness was blocked by an inhibitor of RNA synthesis and by an inhibitor of protein synthesis, but not by an inhibitor of polysaccharide synthesis. Adhesion between preconditioned cells could be inhibited by pretreatment with functionally univalent succinylated concanavalin A or with extracts from preconditioned cells of the opposite mating type. These results confirm in a quantitative manner that the recognition between conjugating cells of S. cerevisiae is a developmentally regulated event that is under the control of the mating type locus.

Adhesiveness↗

PubMed1976

Effects of mating on serum LH, FSH, and prolactin and accessory tissue weight in male rats.

The literature reveals contradictory data regarding whether or not male release LH acutely following coitus. Since it has been shown that repeated mating increases accessory sex organ weight, suggesting induction of gonadotrophin release, it seemed of interest to reinvestigate the issue. Male rats were divided into two groups: the mated group was provided with frequent mating ("experiencing") trials; the unmated group served as cage controls which received no sexual contact throughout the entire experiment. All rats were provided with chronic jugular cannulae. One set of serum samples was taken from each rat at 85 days, the second set at 115 days. On the two evening when sampling took place the mated rats were subdivided into three groups: "chamber" (placed in mating arena alone), "mount" (allowed two to five mounts, but no intromission), and "ejaculation" (mated through entire copulatory sequence). Serum sampling took place every 15 min during the hour following completion of mating (defined in the "ejaculation" group). On the day following the second sampling, autopsies were performed, and terminal serum samples were taken. LH, FSH, and prolactin were measured by radioimmunoassay. There were no significant differences in any hormone among the groups during the hour following mating nor in the terminal sample. However, the mated rats showed significantly greater seminal vesicle and ventral prostate weights than the cage controls at autopsy. Several hypotheses are offered to account for the latter findings.

Animals↗

PubMed2025

Major histocompatibility complex class IIB disassortative mate choice in a genetically monogamous seabird.

Among species reproducing sexually, mating strategies represent a major component of individual fitness. The major histocompatibility complex (MHC) is an extremely diverse set of genes responsible for immunological recognition and defence against pathogens. Although dissimilarity between mates at the major histocompatibility complex has been proposed to drive mate choice through increased offspring pathogen resistance, evidence is mixed. In addition, explorations of the role of the major histocompatibility complex in other mating strategies, such as divorce, are rare. We investigated whether dissimilarity at the major histocompatibility complex class IIB is associated with mate choice and divorce probability in the genetically monogamous black-legged kittiwake (Rissa tridactyla). We found that first-time male breeders, as well as divorced males, were paired with females more dissimilar at the major histocompatibility complex class IIB than expected under random mating. We did not find evidence for mate choice based on major histocompatibility complex class IIB dissimilarity when considering females. In addition, in the studied population, divorce probability was very low compared with other populations and did not significantly vary with the dissimilarity of the pair at the major histocompatibility complex class IIB. Our results pave the way to a better understanding of the complex role of major histocompatibility complex dissimilarity in mating decisions of species displaying mutual choice and biparental care.

Animals↗

PubMed2026

REVIEW: CAUSES AND CONSEQUENCES OF DOING IT WITH ONESELF-SYNTHESIS AND META-ANALYSIS OF NEODERMATAN HERMAPHRODITIC MATING SYSTEMS.

Hermaphroditic mating systems profoundly influence evolution, yet in parasitic flatworms (Neodermata) they remain strikingly understudied. For decades, sweeping claims have oscillated between pervasive selfing and near-universal outcrossing, reflecting a lack of comprehensive synthesis. This review, the first in more than 40 yr, integrates nearly a century of research, from early observational studies to modern genetic analyses, to reveal a far more nuanced picture. Our meta-analysis of population-genetic data shows a sharp departure from the bimodal selfing patterns typical of plants and other hermaphroditic animals: neodermatan parasites are strongly skewed toward outcrossing. We link variation in mating systems to parasite demography and life-history traits, especially in species exhibiting mixed mating or elevated selfing. Current evidence suggests outcrossing is common, but taxonomic and life-history gaps preclude definitive conclusions. Beyond patterns and causes, we explore evolutionary consequences ranging from fitness costs such as inbreeding depression to trait evolution, including delayed selfing, sex allocation, and complex life cycles. Evidence for inbreeding depression is mixed and limited, yet emerging approaches using selfing-rate comparisons offer promising avenues for future research. Notably, demographic constraints, such as infection intensity and life-cycle architecture, often explain mixed mating without invoking selection, challenging classical models. Similarly limited in number, studies on sex allocation indicate that hermaphroditic mating systems can shape reproductive investment, with patterns consistent with local sperm competition in some taxa. By consolidating historical observations with modern genetic insights, this review provides the most comprehensive synthesis of hermaphroditic mating systems in the Neodermata to date. We highlight critical gaps in taxonomic coverage and experimental data and point to future opportunities for integrating genomic approaches with ecological and demographic frameworks. Such integration will be essential to illuminate how mating systems shape parasite evolution and to resolve long-standing questions about the persistence of mixed mating despite theoretical expectations.

Animals↗

PubMed1976

The behavioral phenotype and mating behavior of two inbred strains of Drosophila melanogaster.

Time to copulation was measured in matings within and between two inbred Drosophila melanogaster strains, Edinburgh (E) and 6C/L, using groups of one or five flies of each sex. The E males, which mated faster, usually mate with E females, which are less likely to be fertilized and have fewer progeny whose adult viability is lower. Although generally E males mated far faster with E females than did 6C/L males, there was no difference between the males when with 6C/L females. This need not imply any mating discrimination by E females, but only differences between the strains in the use of preening as a general repulsion movement toward other flies. It is suggested that a greater variety of behavioral and other characteristics (the "behavioral phenotype") should be considered in studies of mating speed and assortative mating, especially where mating speed is being considered as a major component of fitness.

Animals↗

PubMed1978

Influence of beta-alanine on mating and territorialism in Drosophila melanogaster.

Effects of beta-alanine on mating behavior and aggression were studied in Drosophila melanogaster using the following competitive pairs: (1) homozygous black (b/b) flies, in which beta-alanine synthesis is decreased, vs. alanine is blocked vs. wild-type (e+/e+) flies; (2) dark flies, in which beta-alanine incorporation is reduced, owing mainly to chromosome 3, vs. light flies collected from the same population as were the dark flies; (3) homozygous black (b/b) flies, in which beta-alanine synthesis is decreased, vs. beta-alanine-infected b/b flies, which are phenocopies of wild-type flies. The behavior of mixed-sex groups was studied in a large, illumination-graded observation chamber containing food and in small uniformly illuminated cells also containing food. The relative competitive mating abilities of these types were measured in both experimental conditions. Uninjected black flies, but not injected ones, showed weak and unsteady gait and weak wing extension. In ebony these abnormalities were more extreme. Dark flies did not show these abnormalities. Accelerated sexual maturation was indicated in males by early onset of courtship and enhanced territorial aggression and in females by earliness of mating. Such acceleration was observed in ebony and dark flies, compared with light flies, and among beta-alanine-injected b/b flies competing with uninjected black flies. Ebony males, although maturing earlier than wild-type males, were less successful than wild-type males in mating. This difference was even greater when the flies were all allowed to mature before competing. Ebony females outmated wild-type females. Dark flies outmated light flies, and beta-alanine-injected b/b males outmated uninjected black males, especially in bright light. Ebony flies mated much longer than wild-type flies, and black flies mated slightly longer than injected b/b flies. There was some spatial isolation of ebony from wild type, dark from light, and beta-alanine-injected from uninjected b/b flies in the illumination-graded observation chamber. Ebony flies more than wild type concentrated near food. Flies were attracted to the current of moist inlet air. They were also attracted to deposited excrement, and males defended such deposits as a mating area, thus showing rudiments of arena behavior in which a mating area away from the oviposition site is defended. Usually, however, the defended area focused on food.

Aggression↗

PubMed1979

Inbreeding and heterogamic mating: an alternative to Averhoff and Richardson.

An alternative explanation to the pheromonal control of mating through chemoreceptor saturation proposed by Averhoff and Richardson (1974) is offered for the apparent rise in heterogamic mating in their experiments, after several generations of full-sib mating. In a multiple-choice mating between two genotypic strains differing in their level of sexual vigor, there is a sequence from heterogamic to homogamic mating. It is proposed that, by reducing mating speed, inbreeding changes the rate of this sequence but not its pattern, so the apparent level of heterogamic mating will increase during inbreeding, for a fixed observation period. This hypothesis was tested using the Kence-Bryant model of mating success.

Animals↗

PubMedDate not supplied

[Macronuclear DNA and total protein contents of mating types I and II of Paramecium primaurelia, during the phase of maturity and the transition to senescence. Preliminary observations].

Concerning the studies on mating type differentiation and life cycle development in Paramecium primaurelia stock 90, both macronuclear DNA and total protein contents have been measured cytofluorometrically in mating type I and mating type II isogenic cell lines growing in logarithmic phase, throughout their maturity period and transition to senescence. The target was to investigate whether the two mating types undergo clonal decline in different times, as the previous studies suggested. The results indicate that, throughout the maturity period, macronuclear DNA and total protein contents vary both in mating type I and mating type II cell lines; moreover, aged phenotypes as the dramatic decrease of both contents, firstly occur in mating type II which, therefore, appears to be submitted to clonal decline before mating type I.

Aging↗

PubMed1976

Analysis of truncated distributions: mating speed in Drosophila melanogaster.

The distribution of mating speeds in wild-type Drosophila melanogaster is shown to be log normal. The analysis of mating speeds by methods for truncated distributions is validated, and unbiased estimates of the mean mating speed, the variance of mating speed, and the proportion of flies capable of ever mating are produced. In pair matings, not all pairs are capable of copulating, given even a 7-day mating period.

Animals↗