Effects of variations in micro-mammal abundance on artificial nest predation in conifer plantations and adjoining deciduous forests

2002 ◽  
Vol 157 (1-3) ◽  
pp. 255-265 ◽  
Author(s):  
Vincent Carignan ◽  
Marc-André Villard
Author(s):  
Paulo Victor Resende dos Santos ◽  
Ingrid Pinheiro Paschoaletto ◽  
Lia Nahomi Kajiki ◽  
Mariana de-Carvalho ◽  
Samara de Albuquerque Teixeira

2009 ◽  
Vol 92 (2) ◽  
pp. 90-95 ◽  
Author(s):  
Víctor López-Flores ◽  
Ian MacGregor-Fors ◽  
Jorge E. Schondube

1999 ◽  
Vol 77 (7) ◽  
pp. 1170-1173 ◽  
Author(s):  
Keith P Lewis ◽  
William A Montevecchi

In artificial-nest studies, Japanese Quail (Coturnix japonica) eggs have been used as surrogates for passerine eggs, although small mammals that prey on passerine eggs may be unable to consume Japanese Quail eggs. To determine the influence of egg size on nest predation in different landscapes on insular Newfoundland, we placed either a Japanese Quail egg or a smaller Chinese Painted Quail (Xexcalfactoris chinensis) egg in artificial ground nests along lakeshore forest edges and along riparian buffer strips. Clay eggs were used to identify nest predators. Levels of predation on nests with Japanese Quail and Chinese Painted Quail eggs were similar. Based on clay eggs, predation was attributed to red squirrels (Tamiasciurus hudsonicus), and we found no evidence that smaller mammals preyed on artificial nests. We conclude that the Japanese Quail egg is acceptable for use in artificial-nest studies in Newfoundland, and we discuss the implications of egg size and small mammals in nest-predation experiments.


2014 ◽  
Vol 59 ◽  
pp. 91-96 ◽  
Author(s):  
Petr Suvorov ◽  
Jana Svobodová ◽  
Tomáš Albrecht

2007 ◽  
Vol 23 (3) ◽  
pp. 519-527 ◽  
Author(s):  
Richard A. Noske ◽  
Sarah Fischer ◽  
Barry W. Brook

2019 ◽  
Vol 69 (2) ◽  
pp. 137-155
Author(s):  
Magne Husby

Abstract Despite nest predation being the most common cause of breeding failure in open-nesting birds, we have little insight into the cues used by nest predators when they search for nests. So far we have assumed that nest-predating birds are visually oriented while mammal predators to a large extent use scent and auditory cues like nestling begging calls. To evaluate how important nestling begging calls are for corvid nest predators searching for nests, I used artificial nests, which made it possible to find the real costs of the begging without mitigation by parental and nestling behavior. I used paired artificial nests, one with and one without nestling begging call playback. Within 10 days, 62.9% of the nests were predated. The analyses showed that nests with begging calls suffered a significantly higher predation rate than nests without begging calls, especially when the nests were placed close to corvid nests. Moreover, nests with begging calls were predated significantly earlier than nests without begging calls. In artificial nest pairs with both nests predated but on different days, nests with begging calls were predated first. In nest pairs with only one predated nest, nests with begging calls were predated most often. This experiment shows that nestling begging calls imply a cost in terms of increased and earlier nest predation, and that corvids use nestling begging calls as a cue to find and depredate bird nests, challenging earlier expectations.


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