Sperm: seminal fluid interactions and the adjustment of sperm quality in relation to female attractiveness

An important predictor of male fitness is the fertilizing efficiency of their ejaculates. Ejaculates are costly to produce and males are predicted to devote greater resources to copulations with reproductively superior females. It is well established that males allocate different numbers of sperm to ejaculates. However, less is known about how males adjust their sperm quality, which has important implications for our understanding of fertilization and the evolution of sexual strategies. Here we test in the fowl, Gallus gallus, whether males adjust their sperm velocity by differentially allocating seminal fluid to copulations with attractive and unattractive females. To disentangle the contributions of sperm and seminal fluid to sperm velocity, we separated and remixed sperm and seminal fluid from ejaculates allocated to females of different attractiveness. We show that dominant males increase the velocity of the sperm they invest in more attractive females by allocating larger ejaculates that contain seminal fluid that increases sperm velocity. Furthermore, we find weak evidence that males also allocate sperm with higher velocity, irrespective of seminal fluid, to more attractive females

Interspecific Germline Transmission of Cultured Primordial Germ Cells

In birds, the primordial germ cell (PGC) lineage separates from the soma within 24 h following fertilization. Here we show that the endogenous population of about 200 PGCs from a single chicken embryo can be expanded one million fold in culture. When cultured PGCs are injected into a xenogeneic embryo at an equivalent stage of development, they colonize the testis. At sexual maturity, these donor PGCs undergo spermatogenesis in the xenogeneic host and become functional sperm. Insemination of semen from the xenogeneic host into females from the donor species produces normal offspring from the donor species. In our model system, the donor species is chicken (Gallus domesticus) and the recipient species is guinea fowl (Numida meleagris), a member of a different avian family, suggesting that the mechanisms controlling proliferation of the germline are highly conserved within birds. From a pragmatic perspective, these data are the basis of a novel strategy to produce endangered species of birds using domesticated hosts that are both tractable and fecund

Annual variation in the concentrations of circulating hormones in capercaillie (Tetrao urogallus).

Seasonal variation in the levels of immunoreactive lutropin (LH), follitropin (FSH), prolactin (PRL), corticosterone (B), thyroxine (T4), and triiodothyronine (T3) was measured in the plasma of male and female capercaillies (Tetrao urogallus, Galliformes) in captivity (latitude N 67 degrees). In male capercaillies there was an increase in the concentrations of LH and FSH beginning in March and reaching their maxima in May, which correlated with the nesting period. The concentration of plasma PRL increased from the end of April and reached its highest level simultaneously with the rapid fall of plasma LH and FSH concentrations. It remained elevated until August, Plasma T4 level was depressed after levels of plasma FSH and LH had reached their maxima and was correlated to simultaneous elevation of plasma PRL level. No dramatic seasonal changes in plasma T3 level were noted. In the female capercaillie no marked changes in plasma FSH and LH concentrations were observed. Although four of six females laid eggs only one of them managed to terminate its nesting successfully; five eggs hatched. Changes in prolactin concentration in females parallel those in males. No marked variations were observed in plasma corticosterone concentrations. On the basis of these results it seems probable that captive female capercaillie show depressed gonadotrophin secretion, resulting in unsuccessful nesting. On the other hand it has to be emphasized that gonadotrophin assays may not be sensitive enough, especially in the female, to measure LH and FSH in the volumes of plasma put in the assays