Experimental evidence for cryptic interference among socially foraging shorebirds

Foraging rate and the distribution of foragers depend on prey distribution in conjunction with interindividual interactions. Generalized functional response models predict intake rates and spatial distributions of foragers on the basis of resource distribution and interference competition. The adequ...

Full description

Bibliographic Details
Published in:Behavioral Ecology
Main Authors: Bijleveld, Allert Imre, Folmer, Eelke Olov, Piersma, Theunis
Format: Article in Journal/Newspaper
Language:English
Published: 2012
Subjects:
Online Access:https://hdl.handle.net/11370/c49e4926-5763-4912-aa01-e089996b8611
https://research.rug.nl/en/publications/c49e4926-5763-4912-aa01-e089996b8611
https://doi.org/10.1093/beheco/ars034
https://pure.rug.nl/ws/files/6780531/2012BehavEcolBijleveldSupp.mpg
https://pure.rug.nl/ws/files/6780532/2012BehavEcolBijleveld.pdf
Description
Summary:Foraging rate and the distribution of foragers depend on prey distribution in conjunction with interindividual interactions. Generalized functional response models predict intake rates and spatial distributions of foragers on the basis of resource distribution and interference competition. The adequacy of these models depends on how well they capture the foragers' essential behavior. In this paper, we report on the results of a foraging experiment designed to examine the mechanisms of interference competition using red knots Calidris canutus that feed on buried bivalves. Red knots are rarely observed to interfere in the field, but this does not imply absence of interference. Our experimental setup minimized resource depletion, which allowed us to quantify interference competition as the decline in intake rate as a function of group size, with prey density and social status as additional treatments. We found that intake rate and searching efficiency decreased with group size and that dominant birds had higher intake rates than subordinates. Additionally, time spent searching for prey increased with group size. The decrease in intake rate was not due to conventional interference mechanisms (such as kleptoparasitism and time spent interacting with conspecifics) but to "cryptic interference," that is, avoidance of physical encounters with conspecifics. To accurately predict intake rates and foraging distributions, theory and models need to account for the possibility that animals anticipate and try to avoid, at some costs, physical encounters with conspecifics (i.e., conflicts that would make conventional interference behavior visible).