Common Terns Sterna hirundo incubating a Red-necked Grebe Podiceps grisegena egg

During a study of Red-necked Grebes Podiceps grisegena in Lake Slagsmyren, Sweden, a pair of Common Terns Sterna hirundo were observed to have placed their two eggs on a deserted, floating nest of a Red-necked Grebe. Prior to this, the grebes had laid one egg of their own in the nest and this egg was included by the terns in their clutch and incubated by them. The species assignment of the odd egg was confirmed with DNA sequencing. A lack of natural nest sites for the terns to use at the lake could have caused this somewhat unusual choice of a nest site. I discuss possible explanations for adopting a foreign egg, including the adaptive behavioural response to roll an egg into the nest bowl to salvage lost eggs, the incubation stimulus that foreign eggs or egg-like objects potentially provide, and the limited egg discrimination abilities of Common Terns. The incubation of a foreign egg may reasonably be assumed to cost energy but to be of little benefit, if any, to the incubator.

Egg discrimination is mediated by individual differences in queen olfactory responsiveness and boldness

Nest parasites attempt to shift the cost of rearing young from themselves to others. Despite strong selection to avoid this exploitation, there is considerable variation among-individuals in susceptibility to nest parasites. We evaluated the effects of individual variation in boldness, aggressiveness, and olfactory responsiveness on egg discrimination in wasps: Polistes metricus, which founds nests as singleton individuals, and P. dominula, which founds nests in small coalitions. Aggressiveness and boldness were evaluated using individuals’ response to mechanical disturbance, and olfactory responsiveness was evaluated using individuals’ tendency to respond to a novel rewarding stimulus. Egg discrimination was evaluated by presenting each queen with a variety of foreign eggs: 1) unaltered eggs laid by the resident (negative control group), 2) eggs produced by the resident female that were removed and replaced (procedural control), 3) eggs of foreign conspecifics (conspecific egg), and 4) eggs of a heterospecific congener (heterospecific egg). Females of both species never rejected untampered eggs and rejected procedural controls in only 35% of cases. Both species were twice as likely (70% rejection rate) to reject eggs of foreign conspecifics or heterospecifics. In P. dominula, bolder individuals and those with low olfactory responsiveness were more likely to reject foreign eggs. In P. metricus, boldness was not associated with egg rejection, but individuals with heightened olfactory responsiveness were more likely to reject foreign eggs. Thus, there are contrasting associations between behavioral phenotypes and egg rejection across species. These results are discussed in light of differences in the colony founding behavior of these species.

Homing and Egg Discrimination in the Western Slimy Salamander,Plethodon albagula(Caudata: Plethodontidae)

In some species of vertebrates egg brooding is a costly form of parental care. Therefore, misdirection of parental care can significantly lower a female’s fitness. Because of the maternal investment and increased survivorship to offspring from egg guarding, a brooding female should home to her nest site after being displaced a short distance and discriminate between her own eggs and eggs from other females. In this study, we experimentally tested, in the field, alternative hypotheses concerning homing ability and egg discrimination in a population of nesting western slimy salamanders (Plethodon albagula). Fourteen brooding females were displaced 1 m to the left or right of their nest sites (determined randomly) for the homing experiment. Furthermore, brooding females (n = 13) were presented with their own clutches, which were displaced 50 cm to the left or right (determined randomly), and unfamiliar egg clutches at their original nest sites. The females were released at an equal distance from both egg clutches. After 24 hours, 12 displaced females (86%) had returned to their own nest sites and were brooding their egg clutches. Also, after 24 hours, nine test females had returned to their own nest sites and were brooding the unfamiliar egg clutches. No control or test females were present at the other new nest site locations. Therefore, we suggest that brooding femaleP. albagulado home to their nest sites and exhibit indirect egg discrimination.

Hosts of avian brood parasites have evolved egg signatures with elevated information content

Hosts of brood-parasitic birds must distinguish their own eggs from parasitic mimics, or pay the cost of mistakenly raising a foreign chick. Egg discrimination is easier when different host females of the same species each lay visually distinctive eggs (egg ‘signatures’), which helps to foil mimicry by parasites. Here, we ask whether brood parasitism is associated with lower levels of correlation between different egg traits in hosts, making individual host signatures more distinctive and informative. We used entropy as an index of the potential information content encoded by nine aspects of colour, pattern and luminance of eggs of different species in two African bird families (Cisticolidae parasitized by cuckoo finches Anomalospiza imberbis , and Ploceidae by diederik cuckoos Chrysococcyx caprius ). Parasitized species showed consistently higher entropy in egg traits than did related, unparasitized species. Decomposing entropy into two variation components revealed that this was mainly driven by parasitized species having lower levels of correlation between different egg traits, rather than higher overall levels of variation in each individual egg trait. This suggests that irrespective of the constraints that might operate on individual egg traits, hosts can further improve their defensive ‘signatures' by arranging suites of egg traits into unpredictable combinations.

Increase of clutch size triggers clutch destruction behaviour in common moorhens (Gallinula chloropus) during the incubation period

Conspecific brood parasitism (CBP) is common in a variety of animal taxa, including birds. In coots (Fulica spp.), and the closely related moorhens (Gallinula spp.), such parasitism is especially common, and hosts experience considerable costs through increased chick competition soon after hatching. Hence, these birds have evolved egg recognition and rejection abilities, e.g., egg counting, burying the foreign eggs, assigning them suboptimal positions within the mixed clutch, or deserting parasitized clutches. For common moorhens (Gallinula chloropus) it has been shown that desertion of parasitized nests pays most at the early egg laying stage. Later on, the costs of desertion exceed the costs of brood parasitism and acceptance is favoured. Here we tested moorhen egg discrimination behaviour during the incubation stage when acceptance of foreign eggs is expected. Four treatments were applied: (1) single added non-mimetic pale blue egg, (2) single added non-mimetic white chicken egg, (3) four foreign conspecific eggs added to the clutch and (4) four foreign conspecific eggs exchanged for four host eggs. Moorhens responded by egg destruction (47%) only to the increased clutch size but not to foreign egg colour and size match. In three nests where egg destruction occurred, all the eggs in the mixed clutch were destroyed by pecking, in two other nests one of the foreign eggs were pecked, while two other nests were deserted. These results are puzzling since moorhens have been shown to possess refined egg recognition abilities. To our knowledge, such destruction of parasitized clutches by moorhens during incubation has not previously been reported. We suggest that after clutch completion, moorhens use increase in clutch size as a cue to determine if they have been parasitized, and some individuals choose to reject parasitic eggs by deserting or destroying the whole clutch.