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Sperm Length (sperm + length)
Selected AbstractsSperm length in sand martins Riparia riparia: a comment on Helfenstein et alJOURNAL OF AVIAN BIOLOGY, Issue 3 2009Oddmund Kleven How long is a sand martin Riparia riparia spermatozoon? In a recent study, Helfenstein et al. (2008) presented data on the intraspecific variation in sperm length, swimming speed and longevity in this species and some interesting correlations between these variables. However, the reported sperm lengths are remarkably short for the species, which casts doubts about whether sperm total length has actually been measured and how the observed relationships should be interpreted. [source] SPERM MORPHOLOGY AND VELOCITY ARE GENETICALLY CODETERMINED IN THE ZEBRA FINCHEVOLUTION, Issue 10 2009Jim Mossman Sperm morphology (size and shape) and sperm velocity are both positively associated with fertilization success, and are expected to be under strong selection. Until recently, evidence for a link between sperm morphology and velocity was lacking, but recent comparative studies have shown that species with high levels of sperm competition have evolved long and fast sperm. It is therefore surprising that evidence for a phenotypic or genetic relationship between length and velocity within species is equivocal, even though sperm competition is played out in the intraspecific arena. Here, we first show that sperm velocity is positively phenotypically correlated with measures of sperm length in the zebra finch Taeniopygia guttata. Second, by using the quantitative genetic "animal model" on a dataset from a multigenerational-pedigreed population, we show that sperm velocity is heritable, and positively genetically correlated to a number of heritable components of sperm length. Therefore, selection for faster sperm will simultaneously lead to the evolution of longer sperm (and vice versa). Our results provide, for the first time, a clear phenotypic and genetic link between sperm length and velocity, which has broad implications for understanding how recently described macroevolutionary patterns in sperm traits have evolved. [source] Co-evolution of male and female reproductive traits across the Bruchidae (Coleoptera)FUNCTIONAL ECOLOGY, Issue 5 2008P. F. Rugman-Jones Summary 1Despite the obvious importance of spermatozoa to individual reproductive success a general explanation of variation in spermatozoan form and function is still lacking. In species with internal fertilization, sperm not only have to interact with the physical and biochemical environment of the female reproductive tract, but frequently face competition from the sperm of rival males. Both sperm competition theory and adaptation to the selective environment of the female reproductive tract have been implicated in the evolution of spermatozoan morphological diversity. 2Using the comparative method, we examine variation in sperm length in relation to (i) sperm competition intensity (as measured by relative testis size) and (ii) female reproductive characters, across 15 species of beetle belonging to the family Bruchidae. 3Stepwise multiple regression within a phylogenetic framework revealed sperm length to be positively correlated with female spermathecal duct length and negatively related to spermathecal volume, but not testes size, indicating that the female reproductive environment rather than sperm competition per se exerts selection on sperm length in this taxonomic group. 4A positive association between testes volume and the volume of the female spermatheca was also evident suggesting correlated evolution of these traits. 5A number of models of sexual selection could lead to the correlated evolution of male and female reproductive characters, although the underlying mechanisms of cause and effect remain elusive. Divergence between species (and populations) in primary reproductive traits is likely to present a significant barrier to hetero-specific fertilization, and thus contribute to reproductive isolation. [source] Sperm length in sand martins Riparia riparia: a comment on Helfenstein et alJOURNAL OF AVIAN BIOLOGY, Issue 3 2009Oddmund Kleven How long is a sand martin Riparia riparia spermatozoon? In a recent study, Helfenstein et al. (2008) presented data on the intraspecific variation in sperm length, swimming speed and longevity in this species and some interesting correlations between these variables. However, the reported sperm lengths are remarkably short for the species, which casts doubts about whether sperm total length has actually been measured and how the observed relationships should be interpreted. [source] Geographic variation in sperm traits reflects predation risk and natural rates of multiple paternity in the guppyJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 6 2010K. E. ELGEE Abstract Guppies (Poecilia reticulata) are models for understanding the interplay between natural and sexual selection. In particular, predation has been implicated as a major force affecting female sexual preferences, male mating tactics and the level of sperm competition. When predation is high, females typically reduce their preferences for showy males and engage more in antipredator behaviours, whereas males exploit these changes by switching from sexual displays to forced matings. These patterns are thought to account for the relatively high levels of multiple paternity in high-predation populations compared to low-predation populations. Here, we assess the possible evolutionary consequences of these patterns by asking whether variation in sperm traits reflect differences in predation intensity among four pairs of Trinidadian populations: four that experience relatively low levels of predation from a gape-limited predator and four that experience relatively high levels of predation from a variety of piscivores. We found that males in high-predation populations had faster swimming sperm with longer midpieces compared to males in low-predation populations. However, we found no differences among males in high- and low-predation populations with respect to sperm number, sperm head length, flagellum length and total sperm length. [source] Sperm competition and maternal effects differentially influence testis and sperm size in Callosobruchus maculatusJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2009L. GAY Abstract The evolutionary factors affecting testis size are well documented, with sperm competition being of major importance. However, the factors affecting sperm length are not well understood; there are no clear theoretical predictions and the empirical evidence is inconsistent. Recently, maternal effects have been implicated in sperm length variation, a finding that may offer insights into its evolution. We investigated potential proximate and microevolutionary factors influencing testis and sperm size in the bruchid beetle Callosobruchus maculatus using a combined approach of an artificial evolution experiment over 90 generations and an environmental effects study. We found that while polyandry seems to select for larger testes, it had no detectable effect on sperm length. Furthermore, population density, a proximate indicator of sperm competition risk, was not significantly associated with sperm length or testis size variation. However, there were strong maternal effects influencing sperm length. [source] Sperm design and function in the redside dace Clinostomus elongatusJOURNAL OF FISH BIOLOGY, Issue 4 2009T. E. Pitcher A study was undertaken to examine sperm morphometry in relation to sperm velocity and sperm longevity in the redside dace Clinostomus elongatus. There was significant between-male variance in sperm size and shape metrics (total sperm length, sperm head length, flagellum length and sperm head length to width ratio) and positive relationships were found between these morphometrics and sperm velocity. There were no significant relationships found between sperm morphometry and sperm longevity, nor was there a trade-off between sperm velocity and sperm longevity. [source] Consistent significant variation between individual males in spermatozoal morphometryJOURNAL OF ZOOLOGY, Issue 2 2001Edward H. Morrow Abstract Comparative studies show that variation in sperm morphometry across taxa is associated with the environment in which sperm function, and the species' mating pattern dictating the risk of sperm competition. Accordingly, sperm have evolved to function in a non-self environment (in contrast to somatic cells) and sperm morphometry is predicted to be optimized independently of the individual male producing them, but is the result of selective forces arising directly from the fertilization and competitive environment in which sperm will operate. Males within a population are therefore under stabilizing selection to produce an optimal distribution of sperm sizes. The nature of this distribution was explored using consistent techniques to measure detailed sperm morphometry for 10 species in a range of taxa from insects to humans. Although we expected variance in sperm morphometry to be optimized by every individual male through stabilizing selection at a population or species level, we found the exact opposite; for every species examined there was significant variation between individual males in the total lengths of the sperm they produced. A significant variation is reported between individual males for every species in the sizes of each sperm head, mid-piece and flagellum component. The between-male variation exists consistently in wild, domestic and human populations, subject to a wide range of levels of inbreeding. In gryllid crickets sperm length is shown to be male-specific and is repeatable between successive ejaculates. Between-female variation in ova size (data are presented for trout) is explainable by individual female fecundity optimization strategies; however, the adaptive significance of widespread between-individual variance in male gamete size is counter-intuitive and difficult to interpret, particularly as the limited evidence available shows that sperm morphometry is not condition-dependent or resource-constrained. The differences, however, do suggest negligible influences from haploid expression in the development of sperm morphometry , if haplotypic expression were manifested we would expect more profound variation within a male's sperm population (to reflect the inherent within-male variance in haplotypes derived from recombination) rather than the significant between-male differences we found that suggests the diploid control of spermatozoal phenotype [source] Sperm length in sand martins Riparia riparia: a comment on Helfenstein et alJOURNAL OF AVIAN BIOLOGY, Issue 3 2009Oddmund Kleven How long is a sand martin Riparia riparia spermatozoon? In a recent study, Helfenstein et al. (2008) presented data on the intraspecific variation in sperm length, swimming speed and longevity in this species and some interesting correlations between these variables. However, the reported sperm lengths are remarkably short for the species, which casts doubts about whether sperm total length has actually been measured and how the observed relationships should be interpreted. [source] |