The percentage of sperm motility (92-100%), spermatozoan velocity (112 -163 mm·s 21 ) and control hatching rates (83-96%) were evaluated for each of six gold and five green male common carp (Cyprinus carpio). In all 30 possible paired combinations of sperm-competition tests, hatching rates of 90 -97% were achieved. The mean percentage of offspring sired was strongly influenced by the male used (P < 0.001, R 2 5 0.91). The best male sired an average of 88% of the offspring in its competition tests, and the worst male sired only 5%. Spermatozoan-quality parameters could explain only part of the variation in male competitive ability. The male effects alone explained 91.4% of the observed variance, consisting of 17.1% explained by spermatozoan motility and 32.5% by control hatching rates in single fertilizations. Undetermined male effects explained 41.8%. The velocity of spermatozoa had no effect on the outcome of sperm competition. Neither was there any link between spermatozoan velocity and hatching rate in a control hatching test, whereas there was an effect of motility on hatching rate in this same test.Reproduction (
IntroductionSperm competition occurs when the spermatozoa of several males compete for fertilization. Competition is a major force for spermatozoan selection, but its implications for mating systems and on life-history evolution are only just beginning to be understood (Parker 1998, Gage et al. 2004. Trade-offs between gamete characteristics and relative gametic investment has been modelled by evolutionary stable strategy (ESS) approaches, when the optimal strategy for a male depends on the strategy adopted by other individuals in the population , Parker 1998, Petersen & Warner 1998. All of the models assume that males obtain more fertilization success by releasing more sperm, this being done at a cost to investment in other fitness-enhancing functions such as growth, finding additional males, investment in female function, mate defence, territoriality or releasing more sperm in other spawnings. As applied to fish, sperm-competition trials with paternity analysis have been conducted in several salmonid species (Gage et al. 1995, Gile & Ferguson 1995, Liley et al. 2002 and recently also in cyprinids (Kortet et al. 2004, Reichard et al. 2004a, 2004b or other species such as bluegill sunfish (Lepomis macrochirus; Burness et al. 2004). In rainbow trout (Oncorhynchus mykiss) male potency, defined as the ability of males to sire progeny when their sperm is pooled with that of other males, was not affected by the female gametes used, and decreased significantly when sperm concentrations were equalized (Gile & Ferguson 1995). Sperm vary in morphology, behaviour (speed, trajectory, percentage of sperm motility, etc.) and longevity in fishes. Currently, the mechanism of this variation is poorly explained (Cosson et al. 1999). There appear to be intraspecific differences that may correlate with male-mating type in Atlantic salmon (Salmo salar; Gage et al. 1995). Fishes show one of the widest ranges ...