We compared 26 hand-reared grey partridges given an experimental infection of the caecal nematode Heterakis gallinarum with 26 uninfected ones. Under laboratory conditions after 91 days, there were no measurable clinical effects of the infection. We found no effect of treatment on the amount of food eaten or on caecal dropping production. However, treated birds, in particular females, developed slightly lower body mass (around 2%) compared to the controls. At post-mortem examination, we found a positive relationship between breast muscle mass and the number of worms collected from the caeca of treated birds. Treated birds with no worms when examined had smaller breast muscle mass (4·6%) compared to the uninfected control birds. These results are largely different to those found in a similar study that documented significant negative impacts on most of these factors in 8 infected birds compared to 6 controls. Its findings were used in a published model to support a hypothesis that H. gallinarum maintained in the environment by common pheasants, the primary host for this worm, could negatively affect wild grey partridge productivity and survival. In the same model our data would not support this hypothesis. Possible explanations for the different results from the 2 experiments are discussed. Together they suggest that only in certain, as yet unidentified circumstances, could experimental H. gallinarum infections have deleterious effects on hand-reared grey partridges.

If the deleterious effects of non-specific parasites are greater on vulnerable host species than on reservoir host species then exclusion of the vulnerable host through apparent competition is more likely. Evidence suggests that such a mechanism occurs in interactions between the ring-necked pheasant (Phasianus colchicus), the grey partridge (Perdix perdix), and their shared caecal nematode Heterakis gallinarum. Modelling of the system predicts that the reduced parasite impact on the pheasant compared to the partridge results in the force of infection transmitted from pheasants to partridges being sufficient to cause partridge exclusion. Since the parasite impacts are currently estimated from correlational work, controlled infections were conducted to experimentally compare the impact of H. gallinarum on the two hosts and verify cause and effect. While challenged partridges showed reduced mass gain, decreased food consumption, and impaired caecal activity, in comparison to controls, the only detectable effect of parasite challenge on the pheasant was impaired caecal activity. The impact of H. gallinarum on challenged partridges conforms with previous correlational data, supporting the prediction that parasite-mediated apparent competition with the ring-necked pheasant may result in grey partridge exclusion. However, the observed decrease in the caecal activity of challenged pheasants could imply that H. gallinarum may also have an impact on the fecundity and survival of pheasants in the wild, particularly if food is limiting. If this is the case, the associated decrease in the force of infection to which the partridge is exposed may be sufficient to change the model prediction from partridge exclusion to pheasant and partridge coexistence.

Patterns of nematode fecundity were investigated for infections of the caecal worm Heterakis gallinarum in the ring-necked pheasant (Phasianus colchicus). Worm length was a good predictor of parasite fecundity. After controlling for worm length no other factors, including parasite intensity, were related to worm fecundity. Density dependence in worm size was detected in natural infections at parasite intensities above a threshold of 96 worms (worm size decreased with increasing parasite intensity). However, below this threshold, worm size actually decreased with decreasing parasite intensity (inverse density dependence). The interaction between density dependence and inverse density dependence in regulating the development and subsequent fecundity of H. gallinarum worms in ring-necked pheasants was demonstrated in an infection experiment. Density dependence was observed in the stunted growth of worms in heavily infected hosts, relative to worms in lightly infected hosts. Inverse density dependence in worm size was the common pattern across hosts by the end of the experiment, when parasite intensities were below the density dependence threshold. This is the first study to document both density dependence and inverse density dependence in parasite fecundity in the same host–helminth system.