Intraspecific nest parasitism was studied in a group of colonial Red-breasted Mergansers (Mergus serrator) nesting on the Tern Islands of Kouchibouguac National Park in New Brunswick in 1992. Nest parasitism is very common in this colony, and may influence the high rate of nest abandonment observed. Emphasis was placed on determining rates of successful parasitism (i.e. eggs added during the laying period of the hen at that nest), which are evolutionarily significant, and can easily go undetected. Three methods were used to determine if a nest contained egg(s) from another hen: abnormally large clutch size: more than one egg laid per day: and comparisons of DNA fingerprints of the hen versus putative chicks. When eggs were added to a nest during incubation, the nest was also labelled parasitized, but such eggs were not fully incubated (non-term) and thus were not successful. A new method of blood sampling ducklings in pipped eggs was tested and found to have negative effects on survival. As many as 14.8% (13/88) of the ducklings sampled subsequently died. Researchers wishing to use this method should proceed with caution. DNA fingerprinting determined that 50.0% of nests tested (6/12) were successfully parasitized. Two of six parasitized nests would have gone undetected using the other criteria to detect parasitism, thus proving the value of DNA fingerprinting. Of hatched young genetically analyzed, 30.9% (17/55) were parasitic. Nest parasitism appears to be an alternative breeding strategy in this population. Extra-pair copulation, previously unrecorded in this species, was discovered through DNA fingerprinting in two of four nests analyzed.

The rate of intraspecific nest parasitism was determined for a colony of Red-breasted Mergansers (Mergus serrator) nesting on the Tern Islands in Kouchibouguac National Park, New Brunswick. In order to recognize instances of nest parasitism, field criteria and microsatellite analysis testing for parentage between attending hens and the eggs in their nests were used. Traditionally, molecular analysis has involved collecting blood samples from females and offspring, however, for the purpose of this study, DNA was extracted successfully from feathers, egg membranes, and unhatched embryos which were collected during the summers of 1999 and 2000. A total of 8 primer pairs which amplified microsatellite loci in closely related avian species were tested (Sfimu-2, Sfimu-3, Sfimu-4, Sfimu-5, Sfimu-6, Sfimu-7, Bcamu-6, and Alamu-1). Four of these primers produced product of the expected size (Sfimu-3, Sfimu-4, Sfimu-7, and Bcamu-6). Amplification of these loci, however was inconsistent and subsequent sequence analysis revealed that the amplicons did not contain tandem repeats and therefore were not useful in genotyping. From field criteria we were able to establish rates of parasitism of 46% and 44% for each season. Rates of parasitism tended to be higher at the beginning of the season, compared to nests initiated later. Field criteria bring support to several hypotheses on causes of nest parasitism, indicating that more than one may influence rates of parasitism in a population.

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